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		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=Rohypnol&amp;diff=13043</id>
		<title>Rohypnol</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=Rohypnol&amp;diff=13043"/>
		<updated>2007-12-05T11:52:43Z</updated>

		<summary type="html">&lt;p&gt;Wwl06: /* References */&lt;/p&gt;
&lt;hr /&gt;
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&amp;lt;!-- This template has been defined after elaborate discussion in the Chemicals Wikiproject. Please do not add, deleted or otherwise change it unless after due discussion in [[wikipedia talk:WikiProject Chemicals]] --&amp;gt;&lt;br /&gt;
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|-&lt;br /&gt;
! {{chembox header}} | General&lt;br /&gt;
|- &lt;br /&gt;
| [http://en.wikipedia.org/wiki/IUPAC Systematic name]&lt;br /&gt;
| 6-(2-fluorophenyl)-2-methyl-9-nitro-2,&lt;br /&gt;
5-diazabicyclo[5.4.0]undeca-5,8,10,12-&lt;br /&gt;
tetraen-3-one&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Chemical_formula Molecular formula]&lt;br /&gt;
| C16H12FN3O3&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Molar_mass Molar mass]&lt;br /&gt;
| 313.3&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
| Appearance&lt;br /&gt;
| White, light yellow crystalline powder&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/CAS_registry_number CAS number]&lt;br /&gt;
| 1622-62-4&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Properties&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Solubility Solubility]&lt;br /&gt;
| Almost insoluble in water but soluble in alcohol&amp;lt;!--  at least put miscible with, not soluble in --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
&amp;lt;!-- | Other solvents e.g. [[ethanol]], [[acetone]] --&amp;gt;&lt;br /&gt;
&amp;lt;!-- | solubility info on other solvents --&amp;gt;&lt;br /&gt;
&amp;lt;!-- |- --&amp;gt;&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Melting_point Melting point]&lt;br /&gt;
| 168-172 C &amp;lt;!-- (mention any decomposition) --&amp;gt;&lt;br /&gt;
|}&lt;br /&gt;
===Rohypnol (Flunitrazepam) ===&lt;br /&gt;
&amp;lt;jmol&amp;gt;&lt;br /&gt;
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&lt;br /&gt;
&lt;br /&gt;
Rohypnol is a sedative and belongs to a class of drugs known as the benzodiazepines which depress the central nervous system. It is the trade name for a compound known as flunitrazepam. The drug can be taken in a pill (1 and 2mg), crushed up and snorted or dissolved in a drink (alcohol). Rohypnol is manufactured worldwide for medical and therapeutic use but its popularity amongst drug users has rapidly increased and thus is referred to as a ‘Club Drug’ along with Ketamine, LSD and MDMA.&lt;br /&gt;
&lt;br /&gt;
==Synthesis==&lt;br /&gt;
&lt;br /&gt;
Flunitrazepam was first synthesised from (2-fluoro)-methylbenzene.&lt;br /&gt;
&lt;br /&gt;
==Mechanism of action==&lt;br /&gt;
&lt;br /&gt;
Rohypnol is lipophlic and when it is ingested, it is absorbed quickly into the bloodstream and enters the brain via oxidative pathways. The chemical is metabolised rapidly by enzymes (main one being CYP3A4) and binds to nerve receptors that are involved in co-ordination, memory and anxiety. In the absence of Rohypnol, the GABA neurotransmitter binds to these nerve receptors and reduces the activity in the brain. However, when Rohypnol is present it binds to another site (not the binding site) of GABA which slows down the nerve activity in the brain more efficiently. This enhancement of the GABA effect makes Rohypnol a ‘positive allosteric modulator’.&lt;br /&gt;
&lt;br /&gt;
As mentioned previously, Rohypnol is very rapidly absorbed and carried hepatically around the body and peak plasma concentrations occur after 40 minutes from ingestion and thus are a very fast acting benzodiazepine. In addition, Rohypnol has a long half life (roughly 18-26 hours) and a long lasting active metabolite so its effects can persist through to the next day. &lt;br /&gt;
&lt;br /&gt;
==Uses==&lt;br /&gt;
&lt;br /&gt;
Recreational&lt;br /&gt;
Rohypnol is grossly misused recreationally both on its own and with other drugs, e.g. with heroin to heighten the effects or after cocaine or methamphetamine use to ease the after effects of the high. It is also used to counteract the unwanted effects of stimulants such as paranoia, jitteriness, etc. It is used most frequently at raves and by high school and university students. Its low cost and availability is responsible for the rapidly growing numbers of Rohypnol users. &lt;br /&gt;
Medical&lt;br /&gt;
In the early 1970s, this drug was first used in hospitals where deep sedation was required. It is prescribed to relieve severe back pain and in the short term treatments of extreme cases of sleep disorders. It is also used therapeutically to calm patients.&lt;br /&gt;
 &lt;br /&gt;
(6)&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| [[Image:270247 rohypnol300.jpg|thumb|Description]]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
==Effects==&lt;br /&gt;
&lt;br /&gt;
As Rohypnol affects the neutosteroid metabolism, it interferes with brain and reproductive system functions. It results in changes to emotional state and motor functions. There are many short term effects from taking Rohypnol, the most common being amnesia. Others include: muscle relaxation, loss of inhibition, ‘drunken’ feeling, reduction in anxiety and hypnotic and euphoric effects. There are also adverse affects such as excessive sedation, impairment of balance and speech, lack of concentration, confusion, hallucinations, impaired psychomotor functions, slurred speech, and gastrointestinal distrurbances. Although it is classed as a depressant, in some individuals it may lead to aggressive behaviour or excitability. &lt;br /&gt;
&lt;br /&gt;
==Risks==&lt;br /&gt;
&lt;br /&gt;
It can be slipped into a drink unnoticed as it is odourless, tasteless and cannot be seen. There is therefore a high risk of a sexual assault and thus this drug is commonly known as the ‘date-rate drug’.&lt;br /&gt;
As the drug slows down the breathing and heart rate it can lead to breathing difficulties and nausea. The addictive nature of Rohypnol means that regular users are likely to develop a physical dependence. In addition, individuals may also develop a psychological dependence and overtime, increased doses are required to produce the same effect. Withdrawal effects are therefore inevitable and with heavy users, abrupt withdrawal can result in psychosis, seizures, severe insomnia and anxiety. When it is mixed with other drugs the adverse effects are heightened and the possibility of overdose is increased. Overdose can lead to excessive sedation, respiratory arrest which it most serious cases can result in coma and death. Comas and seizures are most likely when this sedative is combined with amphetamines.&lt;br /&gt;
When it is used during pregnancy, the lipolphilic Rohypnol penetrates the membranes and thus crosses over into the placenta resulting in a syndrome known as ‘Floppy Infant Syndrome’ when present in high doses.&lt;br /&gt;
&lt;br /&gt;
==Detection==&lt;br /&gt;
&lt;br /&gt;
Amnesia induced by taking this drug means that a victim of date-rape would not be able to provide any information about events that occurred whilst they were under its influence. This is the reason why the use of this drug in sexual assault is so common. The long half life of the drug means that sophisticated technological equipment can detect flunitrazepan and its related compounds in urine samples for up to about 5 days and roughly 30 days in hair.&lt;br /&gt;
&lt;br /&gt;
(1)&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
! Mass Spectrum&lt;br /&gt;
&lt;br /&gt;
! Chromatogram&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| [[Image:Mass Spec of Rohypnol png.PNG|thumb|Description]]&lt;br /&gt;
&lt;br /&gt;
| [[Image:Chromatogram of Flunitrazepam.PNG|thumb|Description]]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
==Legal status==&lt;br /&gt;
&lt;br /&gt;
Rohypnol is a class C drug. It is legal in 60 countries worldwide for medical use. It is available in the UK on private prescription otherwise its possession is illegal. Rohypnol is not legally available even for medical use in the US.&lt;br /&gt;
In 1998, the manufacturing company (Hoffman-Roche) improved the formula of the drug to make it easier to detect. It now contains a blue dye which appears when it is added to a drink and its solubility properties are altered such that it takes longer for it to dissolve into a drink. &lt;br /&gt;
&lt;br /&gt;
==Other names==&lt;br /&gt;
&lt;br /&gt;
Circles, Roach-2, Roofies, Roopies, Rope, R-2, Roaches, Forget-me-pills, Mexican Valium, Baptist Communion, R2-Do-U.&lt;br /&gt;
&lt;br /&gt;
==References==	&lt;br /&gt;
			&lt;br /&gt;
*(1) http://128.255.99.21/publications/archive/hotline/1999/1999_06/rohypnol.xml&lt;br /&gt;
*(2) http://www.streetdrugs.org/rohypnol.htm&lt;br /&gt;
*(3) http://www.drugs.com/rohypnol.html&lt;br /&gt;
*(4) http://earthops.org/rohypnol.php&lt;br /&gt;
*(5) http://en.wikipedia.org/wiki/Flunitrazepam&lt;br /&gt;
*(6) http://news.bbc.co.uk/1/hi/health/medical_notes/270247.stm&lt;/div&gt;</summary>
		<author><name>Wwl06</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=Rohypnol&amp;diff=13042</id>
		<title>Rohypnol</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=Rohypnol&amp;diff=13042"/>
		<updated>2007-12-05T11:52:07Z</updated>

		<summary type="html">&lt;p&gt;Wwl06: /* Uses */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&amp;lt;noinclude&amp;gt;&lt;br /&gt;
&amp;lt;!-- This template has been defined after elaborate discussion in the Chemicals Wikiproject. Please do not add, deleted or otherwise change it unless after due discussion in [[wikipedia talk:WikiProject Chemicals]] --&amp;gt;&lt;br /&gt;
&amp;lt;/noinclude&amp;gt;{| class=&amp;quot;toccolours&amp;quot; border=&amp;quot;1&amp;quot; style=&amp;quot;float: right; clear: right; margin: 0 0 1em 1em; border-collapse: collapse; width: 280px&amp;quot;&lt;br /&gt;
! {{chembox header}} | {{PAGENAME}} &amp;lt;!-- replace if not identical with the article name --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image:{{PAGENAME}}.jpg|200px|{{PAGENAME}}]] &amp;lt;!-- replace if not identical with the pagename --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | General&lt;br /&gt;
|- &lt;br /&gt;
| [http://en.wikipedia.org/wiki/IUPAC Systematic name]&lt;br /&gt;
| 6-(2-fluorophenyl)-2-methyl-9-nitro-2,&lt;br /&gt;
5-diazabicyclo[5.4.0]undeca-5,8,10,12-&lt;br /&gt;
tetraen-3-one&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Chemical_formula Molecular formula]&lt;br /&gt;
| C16H12FN3O3&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Molar_mass Molar mass]&lt;br /&gt;
| 313.3&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
| Appearance&lt;br /&gt;
| White, light yellow crystalline powder&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/CAS_registry_number CAS number]&lt;br /&gt;
| 1622-62-4&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Properties&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Solubility Solubility]&lt;br /&gt;
| Almost insoluble in water but soluble in alcohol&amp;lt;!--  at least put miscible with, not soluble in --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
&amp;lt;!-- | Other solvents e.g. [[ethanol]], [[acetone]] --&amp;gt;&lt;br /&gt;
&amp;lt;!-- | solubility info on other solvents --&amp;gt;&lt;br /&gt;
&amp;lt;!-- |- --&amp;gt;&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Melting_point Melting point]&lt;br /&gt;
| 168-172 C &amp;lt;!-- (mention any decomposition) --&amp;gt;&lt;br /&gt;
|}&lt;br /&gt;
===Rohypnol (Flunitrazepam) ===&lt;br /&gt;
&amp;lt;jmol&amp;gt;&lt;br /&gt;
&amp;lt;jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;size&amp;gt;200&amp;lt;/size&amp;gt;&lt;br /&gt;
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M  END&lt;br /&gt;
title1&lt;br /&gt;
title2&lt;br /&gt;
&lt;br /&gt;
M  END&amp;lt;/inlineContents&amp;gt;&lt;br /&gt;
&amp;lt;/jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;/jmol&amp;gt;&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
Rohypnol is a sedative and belongs to a class of drugs known as the benzodiazepines which depress the central nervous system. It is the trade name for a compound known as flunitrazepam. The drug can be taken in a pill (1 and 2mg), crushed up and snorted or dissolved in a drink (alcohol). Rohypnol is manufactured worldwide for medical and therapeutic use but its popularity amongst drug users has rapidly increased and thus is referred to as a ‘Club Drug’ along with Ketamine, LSD and MDMA.&lt;br /&gt;
&lt;br /&gt;
==Synthesis==&lt;br /&gt;
&lt;br /&gt;
Flunitrazepam was first synthesised from (2-fluoro)-methylbenzene.&lt;br /&gt;
&lt;br /&gt;
==Mechanism of action==&lt;br /&gt;
&lt;br /&gt;
Rohypnol is lipophlic and when it is ingested, it is absorbed quickly into the bloodstream and enters the brain via oxidative pathways. The chemical is metabolised rapidly by enzymes (main one being CYP3A4) and binds to nerve receptors that are involved in co-ordination, memory and anxiety. In the absence of Rohypnol, the GABA neurotransmitter binds to these nerve receptors and reduces the activity in the brain. However, when Rohypnol is present it binds to another site (not the binding site) of GABA which slows down the nerve activity in the brain more efficiently. This enhancement of the GABA effect makes Rohypnol a ‘positive allosteric modulator’.&lt;br /&gt;
&lt;br /&gt;
As mentioned previously, Rohypnol is very rapidly absorbed and carried hepatically around the body and peak plasma concentrations occur after 40 minutes from ingestion and thus are a very fast acting benzodiazepine. In addition, Rohypnol has a long half life (roughly 18-26 hours) and a long lasting active metabolite so its effects can persist through to the next day. &lt;br /&gt;
&lt;br /&gt;
==Uses==&lt;br /&gt;
&lt;br /&gt;
Recreational&lt;br /&gt;
Rohypnol is grossly misused recreationally both on its own and with other drugs, e.g. with heroin to heighten the effects or after cocaine or methamphetamine use to ease the after effects of the high. It is also used to counteract the unwanted effects of stimulants such as paranoia, jitteriness, etc. It is used most frequently at raves and by high school and university students. Its low cost and availability is responsible for the rapidly growing numbers of Rohypnol users. &lt;br /&gt;
Medical&lt;br /&gt;
In the early 1970s, this drug was first used in hospitals where deep sedation was required. It is prescribed to relieve severe back pain and in the short term treatments of extreme cases of sleep disorders. It is also used therapeutically to calm patients.&lt;br /&gt;
 &lt;br /&gt;
(6)&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| [[Image:270247 rohypnol300.jpg|thumb|Description]]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
==Effects==&lt;br /&gt;
&lt;br /&gt;
As Rohypnol affects the neutosteroid metabolism, it interferes with brain and reproductive system functions. It results in changes to emotional state and motor functions. There are many short term effects from taking Rohypnol, the most common being amnesia. Others include: muscle relaxation, loss of inhibition, ‘drunken’ feeling, reduction in anxiety and hypnotic and euphoric effects. There are also adverse affects such as excessive sedation, impairment of balance and speech, lack of concentration, confusion, hallucinations, impaired psychomotor functions, slurred speech, and gastrointestinal distrurbances. Although it is classed as a depressant, in some individuals it may lead to aggressive behaviour or excitability. &lt;br /&gt;
&lt;br /&gt;
==Risks==&lt;br /&gt;
&lt;br /&gt;
It can be slipped into a drink unnoticed as it is odourless, tasteless and cannot be seen. There is therefore a high risk of a sexual assault and thus this drug is commonly known as the ‘date-rate drug’.&lt;br /&gt;
As the drug slows down the breathing and heart rate it can lead to breathing difficulties and nausea. The addictive nature of Rohypnol means that regular users are likely to develop a physical dependence. In addition, individuals may also develop a psychological dependence and overtime, increased doses are required to produce the same effect. Withdrawal effects are therefore inevitable and with heavy users, abrupt withdrawal can result in psychosis, seizures, severe insomnia and anxiety. When it is mixed with other drugs the adverse effects are heightened and the possibility of overdose is increased. Overdose can lead to excessive sedation, respiratory arrest which it most serious cases can result in coma and death. Comas and seizures are most likely when this sedative is combined with amphetamines.&lt;br /&gt;
When it is used during pregnancy, the lipolphilic Rohypnol penetrates the membranes and thus crosses over into the placenta resulting in a syndrome known as ‘Floppy Infant Syndrome’ when present in high doses.&lt;br /&gt;
&lt;br /&gt;
==Detection==&lt;br /&gt;
&lt;br /&gt;
Amnesia induced by taking this drug means that a victim of date-rape would not be able to provide any information about events that occurred whilst they were under its influence. This is the reason why the use of this drug in sexual assault is so common. The long half life of the drug means that sophisticated technological equipment can detect flunitrazepan and its related compounds in urine samples for up to about 5 days and roughly 30 days in hair.&lt;br /&gt;
&lt;br /&gt;
(1)&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
! Mass Spectrum&lt;br /&gt;
&lt;br /&gt;
! Chromatogram&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| [[Image:Mass Spec of Rohypnol png.PNG|thumb|Description]]&lt;br /&gt;
&lt;br /&gt;
| [[Image:Chromatogram of Flunitrazepam.PNG|thumb|Description]]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
==Legal status==&lt;br /&gt;
&lt;br /&gt;
Rohypnol is a class C drug. It is legal in 60 countries worldwide for medical use. It is available in the UK on private prescription otherwise its possession is illegal. Rohypnol is not legally available even for medical use in the US.&lt;br /&gt;
In 1998, the manufacturing company (Hoffman-Roche) improved the formula of the drug to make it easier to detect. It now contains a blue dye which appears when it is added to a drink and its solubility properties are altered such that it takes longer for it to dissolve into a drink. &lt;br /&gt;
&lt;br /&gt;
==Other names==&lt;br /&gt;
&lt;br /&gt;
Circles, Roach-2, Roofies, Roopies, Rope, R-2, Roaches, Forget-me-pills, Mexican Valium, Baptist Communion, R2-Do-U.&lt;br /&gt;
&lt;br /&gt;
==References==	&lt;br /&gt;
			&lt;br /&gt;
*(1) http://128.255.99.21/publications/archive/hotline/1999/1999_06/rohypnol.xml&lt;br /&gt;
* http://www.streetdrugs.org/rohypnol.htm&lt;br /&gt;
* http://www.drugs.com/rohypnol.html&lt;br /&gt;
* http://earthops.org/rohypnol.php&lt;br /&gt;
* http://en.wikipedia.org/wiki/Flunitrazepam&lt;/div&gt;</summary>
		<author><name>Wwl06</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=Rohypnol&amp;diff=13041</id>
		<title>Rohypnol</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=Rohypnol&amp;diff=13041"/>
		<updated>2007-12-05T11:51:42Z</updated>

		<summary type="html">&lt;p&gt;Wwl06: /* Uses */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&amp;lt;noinclude&amp;gt;&lt;br /&gt;
&amp;lt;!-- This template has been defined after elaborate discussion in the Chemicals Wikiproject. Please do not add, deleted or otherwise change it unless after due discussion in [[wikipedia talk:WikiProject Chemicals]] --&amp;gt;&lt;br /&gt;
&amp;lt;/noinclude&amp;gt;{| class=&amp;quot;toccolours&amp;quot; border=&amp;quot;1&amp;quot; style=&amp;quot;float: right; clear: right; margin: 0 0 1em 1em; border-collapse: collapse; width: 280px&amp;quot;&lt;br /&gt;
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|-&lt;br /&gt;
! {{chembox header}} | General&lt;br /&gt;
|- &lt;br /&gt;
| [http://en.wikipedia.org/wiki/IUPAC Systematic name]&lt;br /&gt;
| 6-(2-fluorophenyl)-2-methyl-9-nitro-2,&lt;br /&gt;
5-diazabicyclo[5.4.0]undeca-5,8,10,12-&lt;br /&gt;
tetraen-3-one&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Chemical_formula Molecular formula]&lt;br /&gt;
| C16H12FN3O3&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Molar_mass Molar mass]&lt;br /&gt;
| 313.3&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
| Appearance&lt;br /&gt;
| White, light yellow crystalline powder&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/CAS_registry_number CAS number]&lt;br /&gt;
| 1622-62-4&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Properties&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Solubility Solubility]&lt;br /&gt;
| Almost insoluble in water but soluble in alcohol&amp;lt;!--  at least put miscible with, not soluble in --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
&amp;lt;!-- | Other solvents e.g. [[ethanol]], [[acetone]] --&amp;gt;&lt;br /&gt;
&amp;lt;!-- | solubility info on other solvents --&amp;gt;&lt;br /&gt;
&amp;lt;!-- |- --&amp;gt;&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Melting_point Melting point]&lt;br /&gt;
| 168-172 C &amp;lt;!-- (mention any decomposition) --&amp;gt;&lt;br /&gt;
|}&lt;br /&gt;
===Rohypnol (Flunitrazepam) ===&lt;br /&gt;
&amp;lt;jmol&amp;gt;&lt;br /&gt;
&amp;lt;jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;size&amp;gt;200&amp;lt;/size&amp;gt;&lt;br /&gt;
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&amp;lt;script&amp;gt;zoom 80; cpk on;frame 1; move 10 -20 10 0 0 0 0 0 3; delay 1;&amp;lt;/script&amp;gt;&lt;br /&gt;
&amp;lt;inlineContents&amp;gt;Molecule-1&lt;br /&gt;
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M  END&lt;br /&gt;
title1&lt;br /&gt;
title2&lt;br /&gt;
&lt;br /&gt;
M  END&amp;lt;/inlineContents&amp;gt;&lt;br /&gt;
&amp;lt;/jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;/jmol&amp;gt;&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
Rohypnol is a sedative and belongs to a class of drugs known as the benzodiazepines which depress the central nervous system. It is the trade name for a compound known as flunitrazepam. The drug can be taken in a pill (1 and 2mg), crushed up and snorted or dissolved in a drink (alcohol). Rohypnol is manufactured worldwide for medical and therapeutic use but its popularity amongst drug users has rapidly increased and thus is referred to as a ‘Club Drug’ along with Ketamine, LSD and MDMA.&lt;br /&gt;
&lt;br /&gt;
==Synthesis==&lt;br /&gt;
&lt;br /&gt;
Flunitrazepam was first synthesised from (2-fluoro)-methylbenzene.&lt;br /&gt;
&lt;br /&gt;
==Mechanism of action==&lt;br /&gt;
&lt;br /&gt;
Rohypnol is lipophlic and when it is ingested, it is absorbed quickly into the bloodstream and enters the brain via oxidative pathways. The chemical is metabolised rapidly by enzymes (main one being CYP3A4) and binds to nerve receptors that are involved in co-ordination, memory and anxiety. In the absence of Rohypnol, the GABA neurotransmitter binds to these nerve receptors and reduces the activity in the brain. However, when Rohypnol is present it binds to another site (not the binding site) of GABA which slows down the nerve activity in the brain more efficiently. This enhancement of the GABA effect makes Rohypnol a ‘positive allosteric modulator’.&lt;br /&gt;
&lt;br /&gt;
As mentioned previously, Rohypnol is very rapidly absorbed and carried hepatically around the body and peak plasma concentrations occur after 40 minutes from ingestion and thus are a very fast acting benzodiazepine. In addition, Rohypnol has a long half life (roughly 18-26 hours) and a long lasting active metabolite so its effects can persist through to the next day. &lt;br /&gt;
&lt;br /&gt;
==Uses==&lt;br /&gt;
&lt;br /&gt;
Recreational&lt;br /&gt;
Rohypnol is grossly misused recreationally both on its own and with other drugs, e.g. with heroin to heighten the effects or after cocaine or methamphetamine use to ease the after effects of the high. It is also used to counteract the unwanted effects of stimulants such as paranoia, jitteriness, etc. It is used most frequently at raves and by high school and university students. Its low cost and availability is responsible for the rapidly growing numbers of Rohypnol users. &lt;br /&gt;
Medical&lt;br /&gt;
In the early 1970s, this drug was first used in hospitals where deep sedation was required. It is prescribed to relieve severe back pain and in the short term treatments of extreme cases of sleep disorders. It is also used therapeutically to calm patients.&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| [[Image:270247 rohypnol300.jpg|thumb|Description]]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
==Effects==&lt;br /&gt;
&lt;br /&gt;
As Rohypnol affects the neutosteroid metabolism, it interferes with brain and reproductive system functions. It results in changes to emotional state and motor functions. There are many short term effects from taking Rohypnol, the most common being amnesia. Others include: muscle relaxation, loss of inhibition, ‘drunken’ feeling, reduction in anxiety and hypnotic and euphoric effects. There are also adverse affects such as excessive sedation, impairment of balance and speech, lack of concentration, confusion, hallucinations, impaired psychomotor functions, slurred speech, and gastrointestinal distrurbances. Although it is classed as a depressant, in some individuals it may lead to aggressive behaviour or excitability. &lt;br /&gt;
&lt;br /&gt;
==Risks==&lt;br /&gt;
&lt;br /&gt;
It can be slipped into a drink unnoticed as it is odourless, tasteless and cannot be seen. There is therefore a high risk of a sexual assault and thus this drug is commonly known as the ‘date-rate drug’.&lt;br /&gt;
As the drug slows down the breathing and heart rate it can lead to breathing difficulties and nausea. The addictive nature of Rohypnol means that regular users are likely to develop a physical dependence. In addition, individuals may also develop a psychological dependence and overtime, increased doses are required to produce the same effect. Withdrawal effects are therefore inevitable and with heavy users, abrupt withdrawal can result in psychosis, seizures, severe insomnia and anxiety. When it is mixed with other drugs the adverse effects are heightened and the possibility of overdose is increased. Overdose can lead to excessive sedation, respiratory arrest which it most serious cases can result in coma and death. Comas and seizures are most likely when this sedative is combined with amphetamines.&lt;br /&gt;
When it is used during pregnancy, the lipolphilic Rohypnol penetrates the membranes and thus crosses over into the placenta resulting in a syndrome known as ‘Floppy Infant Syndrome’ when present in high doses.&lt;br /&gt;
&lt;br /&gt;
==Detection==&lt;br /&gt;
&lt;br /&gt;
Amnesia induced by taking this drug means that a victim of date-rape would not be able to provide any information about events that occurred whilst they were under its influence. This is the reason why the use of this drug in sexual assault is so common. The long half life of the drug means that sophisticated technological equipment can detect flunitrazepan and its related compounds in urine samples for up to about 5 days and roughly 30 days in hair.&lt;br /&gt;
&lt;br /&gt;
(1)&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
! Mass Spectrum&lt;br /&gt;
&lt;br /&gt;
! Chromatogram&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| [[Image:Mass Spec of Rohypnol png.PNG|thumb|Description]]&lt;br /&gt;
&lt;br /&gt;
| [[Image:Chromatogram of Flunitrazepam.PNG|thumb|Description]]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
==Legal status==&lt;br /&gt;
&lt;br /&gt;
Rohypnol is a class C drug. It is legal in 60 countries worldwide for medical use. It is available in the UK on private prescription otherwise its possession is illegal. Rohypnol is not legally available even for medical use in the US.&lt;br /&gt;
In 1998, the manufacturing company (Hoffman-Roche) improved the formula of the drug to make it easier to detect. It now contains a blue dye which appears when it is added to a drink and its solubility properties are altered such that it takes longer for it to dissolve into a drink. &lt;br /&gt;
&lt;br /&gt;
==Other names==&lt;br /&gt;
&lt;br /&gt;
Circles, Roach-2, Roofies, Roopies, Rope, R-2, Roaches, Forget-me-pills, Mexican Valium, Baptist Communion, R2-Do-U.&lt;br /&gt;
&lt;br /&gt;
==References==	&lt;br /&gt;
			&lt;br /&gt;
*(1) http://128.255.99.21/publications/archive/hotline/1999/1999_06/rohypnol.xml&lt;br /&gt;
* http://www.streetdrugs.org/rohypnol.htm&lt;br /&gt;
* http://www.drugs.com/rohypnol.html&lt;br /&gt;
* http://earthops.org/rohypnol.php&lt;br /&gt;
* http://en.wikipedia.org/wiki/Flunitrazepam&lt;/div&gt;</summary>
		<author><name>Wwl06</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=Rohypnol&amp;diff=13040</id>
		<title>Rohypnol</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=Rohypnol&amp;diff=13040"/>
		<updated>2007-12-05T11:51:01Z</updated>

		<summary type="html">&lt;p&gt;Wwl06: /* Uses */&lt;/p&gt;
&lt;hr /&gt;
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|-&lt;br /&gt;
! {{chembox header}} | General&lt;br /&gt;
|- &lt;br /&gt;
| [http://en.wikipedia.org/wiki/IUPAC Systematic name]&lt;br /&gt;
| 6-(2-fluorophenyl)-2-methyl-9-nitro-2,&lt;br /&gt;
5-diazabicyclo[5.4.0]undeca-5,8,10,12-&lt;br /&gt;
tetraen-3-one&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Chemical_formula Molecular formula]&lt;br /&gt;
| C16H12FN3O3&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Molar_mass Molar mass]&lt;br /&gt;
| 313.3&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
| Appearance&lt;br /&gt;
| White, light yellow crystalline powder&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/CAS_registry_number CAS number]&lt;br /&gt;
| 1622-62-4&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Properties&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Solubility Solubility]&lt;br /&gt;
| Almost insoluble in water but soluble in alcohol&amp;lt;!--  at least put miscible with, not soluble in --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
&amp;lt;!-- | Other solvents e.g. [[ethanol]], [[acetone]] --&amp;gt;&lt;br /&gt;
&amp;lt;!-- | solubility info on other solvents --&amp;gt;&lt;br /&gt;
&amp;lt;!-- |- --&amp;gt;&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Melting_point Melting point]&lt;br /&gt;
| 168-172 C &amp;lt;!-- (mention any decomposition) --&amp;gt;&lt;br /&gt;
|}&lt;br /&gt;
===Rohypnol (Flunitrazepam) ===&lt;br /&gt;
&amp;lt;jmol&amp;gt;&lt;br /&gt;
&amp;lt;jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;size&amp;gt;200&amp;lt;/size&amp;gt;&lt;br /&gt;
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&amp;lt;script&amp;gt;zoom 80; cpk on;frame 1; move 10 -20 10 0 0 0 0 0 3; delay 1;&amp;lt;/script&amp;gt;&lt;br /&gt;
&amp;lt;inlineContents&amp;gt;Molecule-1&lt;br /&gt;
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&amp;lt;/jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;/jmol&amp;gt;&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
Rohypnol is a sedative and belongs to a class of drugs known as the benzodiazepines which depress the central nervous system. It is the trade name for a compound known as flunitrazepam. The drug can be taken in a pill (1 and 2mg), crushed up and snorted or dissolved in a drink (alcohol). Rohypnol is manufactured worldwide for medical and therapeutic use but its popularity amongst drug users has rapidly increased and thus is referred to as a ‘Club Drug’ along with Ketamine, LSD and MDMA.&lt;br /&gt;
&lt;br /&gt;
==Synthesis==&lt;br /&gt;
&lt;br /&gt;
Flunitrazepam was first synthesised from (2-fluoro)-methylbenzene.&lt;br /&gt;
&lt;br /&gt;
==Mechanism of action==&lt;br /&gt;
&lt;br /&gt;
Rohypnol is lipophlic and when it is ingested, it is absorbed quickly into the bloodstream and enters the brain via oxidative pathways. The chemical is metabolised rapidly by enzymes (main one being CYP3A4) and binds to nerve receptors that are involved in co-ordination, memory and anxiety. In the absence of Rohypnol, the GABA neurotransmitter binds to these nerve receptors and reduces the activity in the brain. However, when Rohypnol is present it binds to another site (not the binding site) of GABA which slows down the nerve activity in the brain more efficiently. This enhancement of the GABA effect makes Rohypnol a ‘positive allosteric modulator’.&lt;br /&gt;
&lt;br /&gt;
As mentioned previously, Rohypnol is very rapidly absorbed and carried hepatically around the body and peak plasma concentrations occur after 40 minutes from ingestion and thus are a very fast acting benzodiazepine. In addition, Rohypnol has a long half life (roughly 18-26 hours) and a long lasting active metabolite so its effects can persist through to the next day. &lt;br /&gt;
&lt;br /&gt;
==Uses==&lt;br /&gt;
&lt;br /&gt;
Recreational&lt;br /&gt;
Rohypnol is grossly misused recreationally both on its own and with other drugs, e.g. with heroin to heighten the effects or after cocaine or methamphetamine use to ease the after effects of the high. It is also used to counteract the unwanted effects of stimulants such as paranoia, jitteriness, etc. It is used most frequently at raves and by high school and university students. Its low cost and availability is responsible for the rapidly growing numbers of Rohypnol users. &lt;br /&gt;
Medical&lt;br /&gt;
In the early 1970s, this drug was first used in hospitals where deep sedation was required. It is prescribed to relieve severe back pain and in the short term treatments of extreme cases of sleep disorders. It is also used therapeutically to calm patients.&lt;br /&gt;
&lt;br /&gt;
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|}&lt;br /&gt;
&lt;br /&gt;
==Effects==&lt;br /&gt;
&lt;br /&gt;
As Rohypnol affects the neutosteroid metabolism, it interferes with brain and reproductive system functions. It results in changes to emotional state and motor functions. There are many short term effects from taking Rohypnol, the most common being amnesia. Others include: muscle relaxation, loss of inhibition, ‘drunken’ feeling, reduction in anxiety and hypnotic and euphoric effects. There are also adverse affects such as excessive sedation, impairment of balance and speech, lack of concentration, confusion, hallucinations, impaired psychomotor functions, slurred speech, and gastrointestinal distrurbances. Although it is classed as a depressant, in some individuals it may lead to aggressive behaviour or excitability. &lt;br /&gt;
&lt;br /&gt;
==Risks==&lt;br /&gt;
&lt;br /&gt;
It can be slipped into a drink unnoticed as it is odourless, tasteless and cannot be seen. There is therefore a high risk of a sexual assault and thus this drug is commonly known as the ‘date-rate drug’.&lt;br /&gt;
As the drug slows down the breathing and heart rate it can lead to breathing difficulties and nausea. The addictive nature of Rohypnol means that regular users are likely to develop a physical dependence. In addition, individuals may also develop a psychological dependence and overtime, increased doses are required to produce the same effect. Withdrawal effects are therefore inevitable and with heavy users, abrupt withdrawal can result in psychosis, seizures, severe insomnia and anxiety. When it is mixed with other drugs the adverse effects are heightened and the possibility of overdose is increased. Overdose can lead to excessive sedation, respiratory arrest which it most serious cases can result in coma and death. Comas and seizures are most likely when this sedative is combined with amphetamines.&lt;br /&gt;
When it is used during pregnancy, the lipolphilic Rohypnol penetrates the membranes and thus crosses over into the placenta resulting in a syndrome known as ‘Floppy Infant Syndrome’ when present in high doses.&lt;br /&gt;
&lt;br /&gt;
==Detection==&lt;br /&gt;
&lt;br /&gt;
Amnesia induced by taking this drug means that a victim of date-rape would not be able to provide any information about events that occurred whilst they were under its influence. This is the reason why the use of this drug in sexual assault is so common. The long half life of the drug means that sophisticated technological equipment can detect flunitrazepan and its related compounds in urine samples for up to about 5 days and roughly 30 days in hair.&lt;br /&gt;
&lt;br /&gt;
(1)&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
! Mass Spectrum&lt;br /&gt;
&lt;br /&gt;
! Chromatogram&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| [[Image:Mass Spec of Rohypnol png.PNG|thumb|Description]]&lt;br /&gt;
&lt;br /&gt;
| [[Image:Chromatogram of Flunitrazepam.PNG|thumb|Description]]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
==Legal status==&lt;br /&gt;
&lt;br /&gt;
Rohypnol is a class C drug. It is legal in 60 countries worldwide for medical use. It is available in the UK on private prescription otherwise its possession is illegal. Rohypnol is not legally available even for medical use in the US.&lt;br /&gt;
In 1998, the manufacturing company (Hoffman-Roche) improved the formula of the drug to make it easier to detect. It now contains a blue dye which appears when it is added to a drink and its solubility properties are altered such that it takes longer for it to dissolve into a drink. &lt;br /&gt;
&lt;br /&gt;
==Other names==&lt;br /&gt;
&lt;br /&gt;
Circles, Roach-2, Roofies, Roopies, Rope, R-2, Roaches, Forget-me-pills, Mexican Valium, Baptist Communion, R2-Do-U.&lt;br /&gt;
&lt;br /&gt;
==References==	&lt;br /&gt;
			&lt;br /&gt;
*(1) http://128.255.99.21/publications/archive/hotline/1999/1999_06/rohypnol.xml&lt;br /&gt;
* http://www.streetdrugs.org/rohypnol.htm&lt;br /&gt;
* http://www.drugs.com/rohypnol.html&lt;br /&gt;
* http://earthops.org/rohypnol.php&lt;br /&gt;
* http://en.wikipedia.org/wiki/Flunitrazepam&lt;/div&gt;</summary>
		<author><name>Wwl06</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=File:270247_rohypnol300.jpg&amp;diff=13038</id>
		<title>File:270247 rohypnol300.jpg</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=File:270247_rohypnol300.jpg&amp;diff=13038"/>
		<updated>2007-12-05T11:47:20Z</updated>

		<summary type="html">&lt;p&gt;Wwl06: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;/div&gt;</summary>
		<author><name>Wwl06</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=Rohypnol&amp;diff=13035</id>
		<title>Rohypnol</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=Rohypnol&amp;diff=13035"/>
		<updated>2007-12-05T11:45:40Z</updated>

		<summary type="html">&lt;p&gt;Wwl06: /* References */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&amp;lt;noinclude&amp;gt;&lt;br /&gt;
&amp;lt;!-- This template has been defined after elaborate discussion in the Chemicals Wikiproject. Please do not add, deleted or otherwise change it unless after due discussion in [[wikipedia talk:WikiProject Chemicals]] --&amp;gt;&lt;br /&gt;
&amp;lt;/noinclude&amp;gt;{| class=&amp;quot;toccolours&amp;quot; border=&amp;quot;1&amp;quot; style=&amp;quot;float: right; clear: right; margin: 0 0 1em 1em; border-collapse: collapse; width: 280px&amp;quot;&lt;br /&gt;
! {{chembox header}} | {{PAGENAME}} &amp;lt;!-- replace if not identical with the article name --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image:{{PAGENAME}}.jpg|200px|{{PAGENAME}}]] &amp;lt;!-- replace if not identical with the pagename --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | General&lt;br /&gt;
|- &lt;br /&gt;
| [http://en.wikipedia.org/wiki/IUPAC Systematic name]&lt;br /&gt;
| 6-(2-fluorophenyl)-2-methyl-9-nitro-2,&lt;br /&gt;
5-diazabicyclo[5.4.0]undeca-5,8,10,12-&lt;br /&gt;
tetraen-3-one&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Chemical_formula Molecular formula]&lt;br /&gt;
| C16H12FN3O3&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Molar_mass Molar mass]&lt;br /&gt;
| 313.3&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
| Appearance&lt;br /&gt;
| White, light yellow crystalline powder&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/CAS_registry_number CAS number]&lt;br /&gt;
| 1622-62-4&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Properties&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Solubility Solubility]&lt;br /&gt;
| Almost insoluble in water but soluble in alcohol&amp;lt;!--  at least put miscible with, not soluble in --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
&amp;lt;!-- | Other solvents e.g. [[ethanol]], [[acetone]] --&amp;gt;&lt;br /&gt;
&amp;lt;!-- | solubility info on other solvents --&amp;gt;&lt;br /&gt;
&amp;lt;!-- |- --&amp;gt;&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Melting_point Melting point]&lt;br /&gt;
| 168-172 C &amp;lt;!-- (mention any decomposition) --&amp;gt;&lt;br /&gt;
|}&lt;br /&gt;
===Rohypnol (Flunitrazepam) ===&lt;br /&gt;
&amp;lt;jmol&amp;gt;&lt;br /&gt;
&amp;lt;jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;size&amp;gt;200&amp;lt;/size&amp;gt;&lt;br /&gt;
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&amp;lt;script&amp;gt;zoom 80; cpk on;frame 1; move 10 -20 10 0 0 0 0 0 3; delay 1;&amp;lt;/script&amp;gt;&lt;br /&gt;
&amp;lt;inlineContents&amp;gt;Molecule-1&lt;br /&gt;
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M  END&lt;br /&gt;
title1&lt;br /&gt;
title2&lt;br /&gt;
&lt;br /&gt;
M  END&amp;lt;/inlineContents&amp;gt;&lt;br /&gt;
&amp;lt;/jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;/jmol&amp;gt;&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
Rohypnol is a sedative and belongs to a class of drugs known as the benzodiazepines which depress the central nervous system. It is the trade name for a compound known as flunitrazepam. The drug can be taken in a pill (1 and 2mg), crushed up and snorted or dissolved in a drink (alcohol). Rohypnol is manufactured worldwide for medical and therapeutic use but its popularity amongst drug users has rapidly increased and thus is referred to as a ‘Club Drug’ along with Ketamine, LSD and MDMA.&lt;br /&gt;
&lt;br /&gt;
==Synthesis==&lt;br /&gt;
&lt;br /&gt;
Flunitrazepam was first synthesised from (2-fluoro)-methylbenzene.&lt;br /&gt;
&lt;br /&gt;
==Mechanism of action==&lt;br /&gt;
&lt;br /&gt;
Rohypnol is lipophlic and when it is ingested, it is absorbed quickly into the bloodstream and enters the brain via oxidative pathways. The chemical is metabolised rapidly by enzymes (main one being CYP3A4) and binds to nerve receptors that are involved in co-ordination, memory and anxiety. In the absence of Rohypnol, the GABA neurotransmitter binds to these nerve receptors and reduces the activity in the brain. However, when Rohypnol is present it binds to another site (not the binding site) of GABA which slows down the nerve activity in the brain more efficiently. This enhancement of the GABA effect makes Rohypnol a ‘positive allosteric modulator’.&lt;br /&gt;
&lt;br /&gt;
As mentioned previously, Rohypnol is very rapidly absorbed and carried hepatically around the body and peak plasma concentrations occur after 40 minutes from ingestion and thus are a very fast acting benzodiazepine. In addition, Rohypnol has a long half life (roughly 18-26 hours) and a long lasting active metabolite so its effects can persist through to the next day. &lt;br /&gt;
&lt;br /&gt;
==Uses==&lt;br /&gt;
&lt;br /&gt;
Recreational&lt;br /&gt;
Rohypnol is grossly misused recreationally both on its own and with other drugs, e.g. with heroin to heighten the effects or after cocaine or methamphetamine use to ease the after effects of the high. It is also used to counteract the unwanted effects of stimulants such as paranoia, jitteriness, etc. It is used most frequently at raves and by high school and university students. Its low cost and availability is responsible for the rapidly growing numbers of Rohypnol users. &lt;br /&gt;
Medical&lt;br /&gt;
In the early 1970s, this drug was first used in hospitals where deep sedation was required. It is prescribed to relieve severe back pain and in the short term treatments of extreme cases of sleep disorders. It is also used therapeutically to calm patients. &lt;br /&gt;
&lt;br /&gt;
==Effects==&lt;br /&gt;
&lt;br /&gt;
As Rohypnol affects the neutosteroid metabolism, it interferes with brain and reproductive system functions. It results in changes to emotional state and motor functions. There are many short term effects from taking Rohypnol, the most common being amnesia. Others include: muscle relaxation, loss of inhibition, ‘drunken’ feeling, reduction in anxiety and hypnotic and euphoric effects. There are also adverse affects such as excessive sedation, impairment of balance and speech, lack of concentration, confusion, hallucinations, impaired psychomotor functions, slurred speech, and gastrointestinal distrurbances. Although it is classed as a depressant, in some individuals it may lead to aggressive behaviour or excitability. &lt;br /&gt;
&lt;br /&gt;
==Risks==&lt;br /&gt;
&lt;br /&gt;
It can be slipped into a drink unnoticed as it is odourless, tasteless and cannot be seen. There is therefore a high risk of a sexual assault and thus this drug is commonly known as the ‘date-rate drug’.&lt;br /&gt;
As the drug slows down the breathing and heart rate it can lead to breathing difficulties and nausea. The addictive nature of Rohypnol means that regular users are likely to develop a physical dependence. In addition, individuals may also develop a psychological dependence and overtime, increased doses are required to produce the same effect. Withdrawal effects are therefore inevitable and with heavy users, abrupt withdrawal can result in psychosis, seizures, severe insomnia and anxiety. When it is mixed with other drugs the adverse effects are heightened and the possibility of overdose is increased. Overdose can lead to excessive sedation, respiratory arrest which it most serious cases can result in coma and death. Comas and seizures are most likely when this sedative is combined with amphetamines.&lt;br /&gt;
When it is used during pregnancy, the lipolphilic Rohypnol penetrates the membranes and thus crosses over into the placenta resulting in a syndrome known as ‘Floppy Infant Syndrome’ when present in high doses.&lt;br /&gt;
&lt;br /&gt;
==Detection==&lt;br /&gt;
&lt;br /&gt;
Amnesia induced by taking this drug means that a victim of date-rape would not be able to provide any information about events that occurred whilst they were under its influence. This is the reason why the use of this drug in sexual assault is so common. The long half life of the drug means that sophisticated technological equipment can detect flunitrazepan and its related compounds in urine samples for up to about 5 days and roughly 30 days in hair.&lt;br /&gt;
&lt;br /&gt;
(1)&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
! Mass Spectrum&lt;br /&gt;
&lt;br /&gt;
! Chromatogram&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| [[Image:Mass Spec of Rohypnol png.PNG|thumb|Description]]&lt;br /&gt;
&lt;br /&gt;
| [[Image:Chromatogram of Flunitrazepam.PNG|thumb|Description]]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
==Legal status==&lt;br /&gt;
&lt;br /&gt;
Rohypnol is a class C drug. It is legal in 60 countries worldwide for medical use. It is available in the UK on private prescription otherwise its possession is illegal. Rohypnol is not legally available even for medical use in the US.&lt;br /&gt;
In 1998, the manufacturing company (Hoffman-Roche) improved the formula of the drug to make it easier to detect. It now contains a blue dye which appears when it is added to a drink and its solubility properties are altered such that it takes longer for it to dissolve into a drink. &lt;br /&gt;
&lt;br /&gt;
==Other names==&lt;br /&gt;
&lt;br /&gt;
Circles, Roach-2, Roofies, Roopies, Rope, R-2, Roaches, Forget-me-pills, Mexican Valium, Baptist Communion, R2-Do-U.&lt;br /&gt;
&lt;br /&gt;
==References==	&lt;br /&gt;
			&lt;br /&gt;
*(1) http://128.255.99.21/publications/archive/hotline/1999/1999_06/rohypnol.xml&lt;br /&gt;
* http://www.streetdrugs.org/rohypnol.htm&lt;br /&gt;
* http://www.drugs.com/rohypnol.html&lt;br /&gt;
* http://earthops.org/rohypnol.php&lt;br /&gt;
* http://en.wikipedia.org/wiki/Flunitrazepam&lt;/div&gt;</summary>
		<author><name>Wwl06</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=Rohypnol&amp;diff=13028</id>
		<title>Rohypnol</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=Rohypnol&amp;diff=13028"/>
		<updated>2007-12-05T11:44:29Z</updated>

		<summary type="html">&lt;p&gt;Wwl06: /* References */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&amp;lt;noinclude&amp;gt;&lt;br /&gt;
&amp;lt;!-- This template has been defined after elaborate discussion in the Chemicals Wikiproject. Please do not add, deleted or otherwise change it unless after due discussion in [[wikipedia talk:WikiProject Chemicals]] --&amp;gt;&lt;br /&gt;
&amp;lt;/noinclude&amp;gt;{| class=&amp;quot;toccolours&amp;quot; border=&amp;quot;1&amp;quot; style=&amp;quot;float: right; clear: right; margin: 0 0 1em 1em; border-collapse: collapse; width: 280px&amp;quot;&lt;br /&gt;
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|-&lt;br /&gt;
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|-&lt;br /&gt;
! {{chembox header}} | General&lt;br /&gt;
|- &lt;br /&gt;
| [http://en.wikipedia.org/wiki/IUPAC Systematic name]&lt;br /&gt;
| 6-(2-fluorophenyl)-2-methyl-9-nitro-2,&lt;br /&gt;
5-diazabicyclo[5.4.0]undeca-5,8,10,12-&lt;br /&gt;
tetraen-3-one&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Chemical_formula Molecular formula]&lt;br /&gt;
| C16H12FN3O3&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Molar_mass Molar mass]&lt;br /&gt;
| 313.3&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
| Appearance&lt;br /&gt;
| White, light yellow crystalline powder&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/CAS_registry_number CAS number]&lt;br /&gt;
| 1622-62-4&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Properties&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Solubility Solubility]&lt;br /&gt;
| Almost insoluble in water but soluble in alcohol&amp;lt;!--  at least put miscible with, not soluble in --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
&amp;lt;!-- | Other solvents e.g. [[ethanol]], [[acetone]] --&amp;gt;&lt;br /&gt;
&amp;lt;!-- | solubility info on other solvents --&amp;gt;&lt;br /&gt;
&amp;lt;!-- |- --&amp;gt;&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Melting_point Melting point]&lt;br /&gt;
| 168-172 C &amp;lt;!-- (mention any decomposition) --&amp;gt;&lt;br /&gt;
|}&lt;br /&gt;
===Rohypnol (Flunitrazepam) ===&lt;br /&gt;
&amp;lt;jmol&amp;gt;&lt;br /&gt;
&amp;lt;jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;size&amp;gt;200&amp;lt;/size&amp;gt;&lt;br /&gt;
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&amp;lt;script&amp;gt;zoom 80; cpk on;frame 1; move 10 -20 10 0 0 0 0 0 3; delay 1;&amp;lt;/script&amp;gt;&lt;br /&gt;
&amp;lt;inlineContents&amp;gt;Molecule-1&lt;br /&gt;
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M  END&lt;br /&gt;
title1&lt;br /&gt;
title2&lt;br /&gt;
&lt;br /&gt;
M  END&amp;lt;/inlineContents&amp;gt;&lt;br /&gt;
&amp;lt;/jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;/jmol&amp;gt;&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
Rohypnol is a sedative and belongs to a class of drugs known as the benzodiazepines which depress the central nervous system. It is the trade name for a compound known as flunitrazepam. The drug can be taken in a pill (1 and 2mg), crushed up and snorted or dissolved in a drink (alcohol). Rohypnol is manufactured worldwide for medical and therapeutic use but its popularity amongst drug users has rapidly increased and thus is referred to as a ‘Club Drug’ along with Ketamine, LSD and MDMA.&lt;br /&gt;
&lt;br /&gt;
==Synthesis==&lt;br /&gt;
&lt;br /&gt;
Flunitrazepam was first synthesised from (2-fluoro)-methylbenzene.&lt;br /&gt;
&lt;br /&gt;
==Mechanism of action==&lt;br /&gt;
&lt;br /&gt;
Rohypnol is lipophlic and when it is ingested, it is absorbed quickly into the bloodstream and enters the brain via oxidative pathways. The chemical is metabolised rapidly by enzymes (main one being CYP3A4) and binds to nerve receptors that are involved in co-ordination, memory and anxiety. In the absence of Rohypnol, the GABA neurotransmitter binds to these nerve receptors and reduces the activity in the brain. However, when Rohypnol is present it binds to another site (not the binding site) of GABA which slows down the nerve activity in the brain more efficiently. This enhancement of the GABA effect makes Rohypnol a ‘positive allosteric modulator’.&lt;br /&gt;
&lt;br /&gt;
As mentioned previously, Rohypnol is very rapidly absorbed and carried hepatically around the body and peak plasma concentrations occur after 40 minutes from ingestion and thus are a very fast acting benzodiazepine. In addition, Rohypnol has a long half life (roughly 18-26 hours) and a long lasting active metabolite so its effects can persist through to the next day. &lt;br /&gt;
&lt;br /&gt;
==Uses==&lt;br /&gt;
&lt;br /&gt;
Recreational&lt;br /&gt;
Rohypnol is grossly misused recreationally both on its own and with other drugs, e.g. with heroin to heighten the effects or after cocaine or methamphetamine use to ease the after effects of the high. It is also used to counteract the unwanted effects of stimulants such as paranoia, jitteriness, etc. It is used most frequently at raves and by high school and university students. Its low cost and availability is responsible for the rapidly growing numbers of Rohypnol users. &lt;br /&gt;
Medical&lt;br /&gt;
In the early 1970s, this drug was first used in hospitals where deep sedation was required. It is prescribed to relieve severe back pain and in the short term treatments of extreme cases of sleep disorders. It is also used therapeutically to calm patients. &lt;br /&gt;
&lt;br /&gt;
==Effects==&lt;br /&gt;
&lt;br /&gt;
As Rohypnol affects the neutosteroid metabolism, it interferes with brain and reproductive system functions. It results in changes to emotional state and motor functions. There are many short term effects from taking Rohypnol, the most common being amnesia. Others include: muscle relaxation, loss of inhibition, ‘drunken’ feeling, reduction in anxiety and hypnotic and euphoric effects. There are also adverse affects such as excessive sedation, impairment of balance and speech, lack of concentration, confusion, hallucinations, impaired psychomotor functions, slurred speech, and gastrointestinal distrurbances. Although it is classed as a depressant, in some individuals it may lead to aggressive behaviour or excitability. &lt;br /&gt;
&lt;br /&gt;
==Risks==&lt;br /&gt;
&lt;br /&gt;
It can be slipped into a drink unnoticed as it is odourless, tasteless and cannot be seen. There is therefore a high risk of a sexual assault and thus this drug is commonly known as the ‘date-rate drug’.&lt;br /&gt;
As the drug slows down the breathing and heart rate it can lead to breathing difficulties and nausea. The addictive nature of Rohypnol means that regular users are likely to develop a physical dependence. In addition, individuals may also develop a psychological dependence and overtime, increased doses are required to produce the same effect. Withdrawal effects are therefore inevitable and with heavy users, abrupt withdrawal can result in psychosis, seizures, severe insomnia and anxiety. When it is mixed with other drugs the adverse effects are heightened and the possibility of overdose is increased. Overdose can lead to excessive sedation, respiratory arrest which it most serious cases can result in coma and death. Comas and seizures are most likely when this sedative is combined with amphetamines.&lt;br /&gt;
When it is used during pregnancy, the lipolphilic Rohypnol penetrates the membranes and thus crosses over into the placenta resulting in a syndrome known as ‘Floppy Infant Syndrome’ when present in high doses.&lt;br /&gt;
&lt;br /&gt;
==Detection==&lt;br /&gt;
&lt;br /&gt;
Amnesia induced by taking this drug means that a victim of date-rape would not be able to provide any information about events that occurred whilst they were under its influence. This is the reason why the use of this drug in sexual assault is so common. The long half life of the drug means that sophisticated technological equipment can detect flunitrazepan and its related compounds in urine samples for up to about 5 days and roughly 30 days in hair.&lt;br /&gt;
&lt;br /&gt;
(1)&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
! Mass Spectrum&lt;br /&gt;
&lt;br /&gt;
! Chromatogram&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| [[Image:Mass Spec of Rohypnol png.PNG|thumb|Description]]&lt;br /&gt;
&lt;br /&gt;
| [[Image:Chromatogram of Flunitrazepam.PNG|thumb|Description]]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
==Legal status==&lt;br /&gt;
&lt;br /&gt;
Rohypnol is a class C drug. It is legal in 60 countries worldwide for medical use. It is available in the UK on private prescription otherwise its possession is illegal. Rohypnol is not legally available even for medical use in the US.&lt;br /&gt;
In 1998, the manufacturing company (Hoffman-Roche) improved the formula of the drug to make it easier to detect. It now contains a blue dye which appears when it is added to a drink and its solubility properties are altered such that it takes longer for it to dissolve into a drink. &lt;br /&gt;
&lt;br /&gt;
==Other names==&lt;br /&gt;
&lt;br /&gt;
Circles, Roach-2, Roofies, Roopies, Rope, R-2, Roaches, Forget-me-pills, Mexican Valium, Baptist Communion, R2-Do-U.&lt;br /&gt;
&lt;br /&gt;
==References==	&lt;br /&gt;
			&lt;br /&gt;
*(1) http://128.255.99.21/publications/archive/hotline/1999/1999_06/rohypnol.xml&lt;br /&gt;
* http://www.streetdrugs.org/rohypnol.htm&lt;br /&gt;
* http://www.drugs.com/rohypnol.html&lt;br /&gt;
* http://earthops.org/rohypnol.php&lt;/div&gt;</summary>
		<author><name>Wwl06</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=Rohypnol&amp;diff=13023</id>
		<title>Rohypnol</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=Rohypnol&amp;diff=13023"/>
		<updated>2007-12-05T11:42:59Z</updated>

		<summary type="html">&lt;p&gt;Wwl06: /* References */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&amp;lt;noinclude&amp;gt;&lt;br /&gt;
&amp;lt;!-- This template has been defined after elaborate discussion in the Chemicals Wikiproject. Please do not add, deleted or otherwise change it unless after due discussion in [[wikipedia talk:WikiProject Chemicals]] --&amp;gt;&lt;br /&gt;
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|-&lt;br /&gt;
! {{chembox header}} | General&lt;br /&gt;
|- &lt;br /&gt;
| [http://en.wikipedia.org/wiki/IUPAC Systematic name]&lt;br /&gt;
| 6-(2-fluorophenyl)-2-methyl-9-nitro-2,&lt;br /&gt;
5-diazabicyclo[5.4.0]undeca-5,8,10,12-&lt;br /&gt;
tetraen-3-one&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Chemical_formula Molecular formula]&lt;br /&gt;
| C16H12FN3O3&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Molar_mass Molar mass]&lt;br /&gt;
| 313.3&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
| Appearance&lt;br /&gt;
| White, light yellow crystalline powder&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/CAS_registry_number CAS number]&lt;br /&gt;
| 1622-62-4&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Properties&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Solubility Solubility]&lt;br /&gt;
| Almost insoluble in water but soluble in alcohol&amp;lt;!--  at least put miscible with, not soluble in --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
&amp;lt;!-- | Other solvents e.g. [[ethanol]], [[acetone]] --&amp;gt;&lt;br /&gt;
&amp;lt;!-- | solubility info on other solvents --&amp;gt;&lt;br /&gt;
&amp;lt;!-- |- --&amp;gt;&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Melting_point Melting point]&lt;br /&gt;
| 168-172 C &amp;lt;!-- (mention any decomposition) --&amp;gt;&lt;br /&gt;
|}&lt;br /&gt;
===Rohypnol (Flunitrazepam) ===&lt;br /&gt;
&amp;lt;jmol&amp;gt;&lt;br /&gt;
&amp;lt;jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;size&amp;gt;200&amp;lt;/size&amp;gt;&lt;br /&gt;
&amp;lt;color&amp;gt;white&amp;lt;/color&amp;gt;&lt;br /&gt;
&amp;lt;script&amp;gt;zoom 80; cpk on;frame 1; move 10 -20 10 0 0 0 0 0 3; delay 1;&amp;lt;/script&amp;gt;&lt;br /&gt;
&amp;lt;inlineContents&amp;gt;Molecule-1&lt;br /&gt;
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   -0.2978    1.0695   -0.0067 C   0  0  0  0  0  0  0  0  0  3&lt;br /&gt;
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    0.9533   -5.7735    0.1176 C   0  0  0  0  0  0  0  0  0 23&lt;br /&gt;
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M  END&amp;lt;/inlineContents&amp;gt;&lt;br /&gt;
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&amp;lt;/jmol&amp;gt;&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
Rohypnol is a sedative and belongs to a class of drugs known as the benzodiazepines which depress the central nervous system. It is the trade name for a compound known as flunitrazepam. The drug can be taken in a pill (1 and 2mg), crushed up and snorted or dissolved in a drink (alcohol). Rohypnol is manufactured worldwide for medical and therapeutic use but its popularity amongst drug users has rapidly increased and thus is referred to as a ‘Club Drug’ along with Ketamine, LSD and MDMA.&lt;br /&gt;
&lt;br /&gt;
==Synthesis==&lt;br /&gt;
&lt;br /&gt;
Flunitrazepam was first synthesised from (2-fluoro)-methylbenzene.&lt;br /&gt;
&lt;br /&gt;
==Mechanism of action==&lt;br /&gt;
&lt;br /&gt;
Rohypnol is lipophlic and when it is ingested, it is absorbed quickly into the bloodstream and enters the brain via oxidative pathways. The chemical is metabolised rapidly by enzymes (main one being CYP3A4) and binds to nerve receptors that are involved in co-ordination, memory and anxiety. In the absence of Rohypnol, the GABA neurotransmitter binds to these nerve receptors and reduces the activity in the brain. However, when Rohypnol is present it binds to another site (not the binding site) of GABA which slows down the nerve activity in the brain more efficiently. This enhancement of the GABA effect makes Rohypnol a ‘positive allosteric modulator’.&lt;br /&gt;
&lt;br /&gt;
As mentioned previously, Rohypnol is very rapidly absorbed and carried hepatically around the body and peak plasma concentrations occur after 40 minutes from ingestion and thus are a very fast acting benzodiazepine. In addition, Rohypnol has a long half life (roughly 18-26 hours) and a long lasting active metabolite so its effects can persist through to the next day. &lt;br /&gt;
&lt;br /&gt;
==Uses==&lt;br /&gt;
&lt;br /&gt;
Recreational&lt;br /&gt;
Rohypnol is grossly misused recreationally both on its own and with other drugs, e.g. with heroin to heighten the effects or after cocaine or methamphetamine use to ease the after effects of the high. It is also used to counteract the unwanted effects of stimulants such as paranoia, jitteriness, etc. It is used most frequently at raves and by high school and university students. Its low cost and availability is responsible for the rapidly growing numbers of Rohypnol users. &lt;br /&gt;
Medical&lt;br /&gt;
In the early 1970s, this drug was first used in hospitals where deep sedation was required. It is prescribed to relieve severe back pain and in the short term treatments of extreme cases of sleep disorders. It is also used therapeutically to calm patients. &lt;br /&gt;
&lt;br /&gt;
==Effects==&lt;br /&gt;
&lt;br /&gt;
As Rohypnol affects the neutosteroid metabolism, it interferes with brain and reproductive system functions. It results in changes to emotional state and motor functions. There are many short term effects from taking Rohypnol, the most common being amnesia. Others include: muscle relaxation, loss of inhibition, ‘drunken’ feeling, reduction in anxiety and hypnotic and euphoric effects. There are also adverse affects such as excessive sedation, impairment of balance and speech, lack of concentration, confusion, hallucinations, impaired psychomotor functions, slurred speech, and gastrointestinal distrurbances. Although it is classed as a depressant, in some individuals it may lead to aggressive behaviour or excitability. &lt;br /&gt;
&lt;br /&gt;
==Risks==&lt;br /&gt;
&lt;br /&gt;
It can be slipped into a drink unnoticed as it is odourless, tasteless and cannot be seen. There is therefore a high risk of a sexual assault and thus this drug is commonly known as the ‘date-rate drug’.&lt;br /&gt;
As the drug slows down the breathing and heart rate it can lead to breathing difficulties and nausea. The addictive nature of Rohypnol means that regular users are likely to develop a physical dependence. In addition, individuals may also develop a psychological dependence and overtime, increased doses are required to produce the same effect. Withdrawal effects are therefore inevitable and with heavy users, abrupt withdrawal can result in psychosis, seizures, severe insomnia and anxiety. When it is mixed with other drugs the adverse effects are heightened and the possibility of overdose is increased. Overdose can lead to excessive sedation, respiratory arrest which it most serious cases can result in coma and death. Comas and seizures are most likely when this sedative is combined with amphetamines.&lt;br /&gt;
When it is used during pregnancy, the lipolphilic Rohypnol penetrates the membranes and thus crosses over into the placenta resulting in a syndrome known as ‘Floppy Infant Syndrome’ when present in high doses.&lt;br /&gt;
&lt;br /&gt;
==Detection==&lt;br /&gt;
&lt;br /&gt;
Amnesia induced by taking this drug means that a victim of date-rape would not be able to provide any information about events that occurred whilst they were under its influence. This is the reason why the use of this drug in sexual assault is so common. The long half life of the drug means that sophisticated technological equipment can detect flunitrazepan and its related compounds in urine samples for up to about 5 days and roughly 30 days in hair.&lt;br /&gt;
&lt;br /&gt;
(1)&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
! Mass Spectrum&lt;br /&gt;
&lt;br /&gt;
! Chromatogram&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| [[Image:Mass Spec of Rohypnol png.PNG|thumb|Description]]&lt;br /&gt;
&lt;br /&gt;
| [[Image:Chromatogram of Flunitrazepam.PNG|thumb|Description]]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
==Legal status==&lt;br /&gt;
&lt;br /&gt;
Rohypnol is a class C drug. It is legal in 60 countries worldwide for medical use. It is available in the UK on private prescription otherwise its possession is illegal. Rohypnol is not legally available even for medical use in the US.&lt;br /&gt;
In 1998, the manufacturing company (Hoffman-Roche) improved the formula of the drug to make it easier to detect. It now contains a blue dye which appears when it is added to a drink and its solubility properties are altered such that it takes longer for it to dissolve into a drink. &lt;br /&gt;
&lt;br /&gt;
==Other names==&lt;br /&gt;
&lt;br /&gt;
Circles, Roach-2, Roofies, Roopies, Rope, R-2, Roaches, Forget-me-pills, Mexican Valium, Baptist Communion, R2-Do-U.&lt;br /&gt;
&lt;br /&gt;
==References==	&lt;br /&gt;
			&lt;br /&gt;
*(1) http://128.255.99.21/publications/archive/hotline/1999/1999_06/rohypnol.xml&lt;/div&gt;</summary>
		<author><name>Wwl06</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=Rohypnol&amp;diff=13021</id>
		<title>Rohypnol</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=Rohypnol&amp;diff=13021"/>
		<updated>2007-12-05T11:42:48Z</updated>

		<summary type="html">&lt;p&gt;Wwl06: /* Detection */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&amp;lt;noinclude&amp;gt;&lt;br /&gt;
&amp;lt;!-- This template has been defined after elaborate discussion in the Chemicals Wikiproject. Please do not add, deleted or otherwise change it unless after due discussion in [[wikipedia talk:WikiProject Chemicals]] --&amp;gt;&lt;br /&gt;
&amp;lt;/noinclude&amp;gt;{| class=&amp;quot;toccolours&amp;quot; border=&amp;quot;1&amp;quot; style=&amp;quot;float: right; clear: right; margin: 0 0 1em 1em; border-collapse: collapse; width: 280px&amp;quot;&lt;br /&gt;
! {{chembox header}} | {{PAGENAME}} &amp;lt;!-- replace if not identical with the article name --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image:{{PAGENAME}}.jpg|200px|{{PAGENAME}}]] &amp;lt;!-- replace if not identical with the pagename --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | General&lt;br /&gt;
|- &lt;br /&gt;
| [http://en.wikipedia.org/wiki/IUPAC Systematic name]&lt;br /&gt;
| 6-(2-fluorophenyl)-2-methyl-9-nitro-2,&lt;br /&gt;
5-diazabicyclo[5.4.0]undeca-5,8,10,12-&lt;br /&gt;
tetraen-3-one&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Chemical_formula Molecular formula]&lt;br /&gt;
| C16H12FN3O3&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Molar_mass Molar mass]&lt;br /&gt;
| 313.3&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
| Appearance&lt;br /&gt;
| White, light yellow crystalline powder&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/CAS_registry_number CAS number]&lt;br /&gt;
| 1622-62-4&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Properties&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Solubility Solubility]&lt;br /&gt;
| Almost insoluble in water but soluble in alcohol&amp;lt;!--  at least put miscible with, not soluble in --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
&amp;lt;!-- | Other solvents e.g. [[ethanol]], [[acetone]] --&amp;gt;&lt;br /&gt;
&amp;lt;!-- | solubility info on other solvents --&amp;gt;&lt;br /&gt;
&amp;lt;!-- |- --&amp;gt;&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Melting_point Melting point]&lt;br /&gt;
| 168-172 C &amp;lt;!-- (mention any decomposition) --&amp;gt;&lt;br /&gt;
|}&lt;br /&gt;
===Rohypnol (Flunitrazepam) ===&lt;br /&gt;
&amp;lt;jmol&amp;gt;&lt;br /&gt;
&amp;lt;jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;size&amp;gt;200&amp;lt;/size&amp;gt;&lt;br /&gt;
&amp;lt;color&amp;gt;white&amp;lt;/color&amp;gt;&lt;br /&gt;
&amp;lt;script&amp;gt;zoom 80; cpk on;frame 1; move 10 -20 10 0 0 0 0 0 3; delay 1;&amp;lt;/script&amp;gt;&lt;br /&gt;
&amp;lt;inlineContents&amp;gt;Molecule-1&lt;br /&gt;
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    0.9533   -5.7735    0.1176 C   0  0  0  0  0  0  0  0  0 23&lt;br /&gt;
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M  END&lt;br /&gt;
title1&lt;br /&gt;
title2&lt;br /&gt;
&lt;br /&gt;
M  END&amp;lt;/inlineContents&amp;gt;&lt;br /&gt;
&amp;lt;/jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;/jmol&amp;gt;&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
Rohypnol is a sedative and belongs to a class of drugs known as the benzodiazepines which depress the central nervous system. It is the trade name for a compound known as flunitrazepam. The drug can be taken in a pill (1 and 2mg), crushed up and snorted or dissolved in a drink (alcohol). Rohypnol is manufactured worldwide for medical and therapeutic use but its popularity amongst drug users has rapidly increased and thus is referred to as a ‘Club Drug’ along with Ketamine, LSD and MDMA.&lt;br /&gt;
&lt;br /&gt;
==Synthesis==&lt;br /&gt;
&lt;br /&gt;
Flunitrazepam was first synthesised from (2-fluoro)-methylbenzene.&lt;br /&gt;
&lt;br /&gt;
==Mechanism of action==&lt;br /&gt;
&lt;br /&gt;
Rohypnol is lipophlic and when it is ingested, it is absorbed quickly into the bloodstream and enters the brain via oxidative pathways. The chemical is metabolised rapidly by enzymes (main one being CYP3A4) and binds to nerve receptors that are involved in co-ordination, memory and anxiety. In the absence of Rohypnol, the GABA neurotransmitter binds to these nerve receptors and reduces the activity in the brain. However, when Rohypnol is present it binds to another site (not the binding site) of GABA which slows down the nerve activity in the brain more efficiently. This enhancement of the GABA effect makes Rohypnol a ‘positive allosteric modulator’.&lt;br /&gt;
&lt;br /&gt;
As mentioned previously, Rohypnol is very rapidly absorbed and carried hepatically around the body and peak plasma concentrations occur after 40 minutes from ingestion and thus are a very fast acting benzodiazepine. In addition, Rohypnol has a long half life (roughly 18-26 hours) and a long lasting active metabolite so its effects can persist through to the next day. &lt;br /&gt;
&lt;br /&gt;
==Uses==&lt;br /&gt;
&lt;br /&gt;
Recreational&lt;br /&gt;
Rohypnol is grossly misused recreationally both on its own and with other drugs, e.g. with heroin to heighten the effects or after cocaine or methamphetamine use to ease the after effects of the high. It is also used to counteract the unwanted effects of stimulants such as paranoia, jitteriness, etc. It is used most frequently at raves and by high school and university students. Its low cost and availability is responsible for the rapidly growing numbers of Rohypnol users. &lt;br /&gt;
Medical&lt;br /&gt;
In the early 1970s, this drug was first used in hospitals where deep sedation was required. It is prescribed to relieve severe back pain and in the short term treatments of extreme cases of sleep disorders. It is also used therapeutically to calm patients. &lt;br /&gt;
&lt;br /&gt;
==Effects==&lt;br /&gt;
&lt;br /&gt;
As Rohypnol affects the neutosteroid metabolism, it interferes with brain and reproductive system functions. It results in changes to emotional state and motor functions. There are many short term effects from taking Rohypnol, the most common being amnesia. Others include: muscle relaxation, loss of inhibition, ‘drunken’ feeling, reduction in anxiety and hypnotic and euphoric effects. There are also adverse affects such as excessive sedation, impairment of balance and speech, lack of concentration, confusion, hallucinations, impaired psychomotor functions, slurred speech, and gastrointestinal distrurbances. Although it is classed as a depressant, in some individuals it may lead to aggressive behaviour or excitability. &lt;br /&gt;
&lt;br /&gt;
==Risks==&lt;br /&gt;
&lt;br /&gt;
It can be slipped into a drink unnoticed as it is odourless, tasteless and cannot be seen. There is therefore a high risk of a sexual assault and thus this drug is commonly known as the ‘date-rate drug’.&lt;br /&gt;
As the drug slows down the breathing and heart rate it can lead to breathing difficulties and nausea. The addictive nature of Rohypnol means that regular users are likely to develop a physical dependence. In addition, individuals may also develop a psychological dependence and overtime, increased doses are required to produce the same effect. Withdrawal effects are therefore inevitable and with heavy users, abrupt withdrawal can result in psychosis, seizures, severe insomnia and anxiety. When it is mixed with other drugs the adverse effects are heightened and the possibility of overdose is increased. Overdose can lead to excessive sedation, respiratory arrest which it most serious cases can result in coma and death. Comas and seizures are most likely when this sedative is combined with amphetamines.&lt;br /&gt;
When it is used during pregnancy, the lipolphilic Rohypnol penetrates the membranes and thus crosses over into the placenta resulting in a syndrome known as ‘Floppy Infant Syndrome’ when present in high doses.&lt;br /&gt;
&lt;br /&gt;
==Detection==&lt;br /&gt;
&lt;br /&gt;
Amnesia induced by taking this drug means that a victim of date-rape would not be able to provide any information about events that occurred whilst they were under its influence. This is the reason why the use of this drug in sexual assault is so common. The long half life of the drug means that sophisticated technological equipment can detect flunitrazepan and its related compounds in urine samples for up to about 5 days and roughly 30 days in hair.&lt;br /&gt;
&lt;br /&gt;
(1)&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
! Mass Spectrum&lt;br /&gt;
&lt;br /&gt;
! Chromatogram&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| [[Image:Mass Spec of Rohypnol png.PNG|thumb|Description]]&lt;br /&gt;
&lt;br /&gt;
| [[Image:Chromatogram of Flunitrazepam.PNG|thumb|Description]]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
==Legal status==&lt;br /&gt;
&lt;br /&gt;
Rohypnol is a class C drug. It is legal in 60 countries worldwide for medical use. It is available in the UK on private prescription otherwise its possession is illegal. Rohypnol is not legally available even for medical use in the US.&lt;br /&gt;
In 1998, the manufacturing company (Hoffman-Roche) improved the formula of the drug to make it easier to detect. It now contains a blue dye which appears when it is added to a drink and its solubility properties are altered such that it takes longer for it to dissolve into a drink. &lt;br /&gt;
&lt;br /&gt;
==Other names==&lt;br /&gt;
&lt;br /&gt;
Circles, Roach-2, Roofies, Roopies, Rope, R-2, Roaches, Forget-me-pills, Mexican Valium, Baptist Communion, R2-Do-U.&lt;br /&gt;
&lt;br /&gt;
==References==	&lt;br /&gt;
			&lt;br /&gt;
*http://128.255.99.21/publications/archive/hotline/1999/1999_06/rohypnol.xml&lt;/div&gt;</summary>
		<author><name>Wwl06</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=Rohypnol&amp;diff=13019</id>
		<title>Rohypnol</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=Rohypnol&amp;diff=13019"/>
		<updated>2007-12-05T11:37:36Z</updated>

		<summary type="html">&lt;p&gt;Wwl06: /* Detection */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&amp;lt;noinclude&amp;gt;&lt;br /&gt;
&amp;lt;!-- This template has been defined after elaborate discussion in the Chemicals Wikiproject. Please do not add, deleted or otherwise change it unless after due discussion in [[wikipedia talk:WikiProject Chemicals]] --&amp;gt;&lt;br /&gt;
&amp;lt;/noinclude&amp;gt;{| class=&amp;quot;toccolours&amp;quot; border=&amp;quot;1&amp;quot; style=&amp;quot;float: right; clear: right; margin: 0 0 1em 1em; border-collapse: collapse; width: 280px&amp;quot;&lt;br /&gt;
! {{chembox header}} | {{PAGENAME}} &amp;lt;!-- replace if not identical with the article name --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image:{{PAGENAME}}.jpg|200px|{{PAGENAME}}]] &amp;lt;!-- replace if not identical with the pagename --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | General&lt;br /&gt;
|- &lt;br /&gt;
| [http://en.wikipedia.org/wiki/IUPAC Systematic name]&lt;br /&gt;
| 6-(2-fluorophenyl)-2-methyl-9-nitro-2,&lt;br /&gt;
5-diazabicyclo[5.4.0]undeca-5,8,10,12-&lt;br /&gt;
tetraen-3-one&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Chemical_formula Molecular formula]&lt;br /&gt;
| C16H12FN3O3&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Molar_mass Molar mass]&lt;br /&gt;
| 313.3&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
| Appearance&lt;br /&gt;
| White, light yellow crystalline powder&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/CAS_registry_number CAS number]&lt;br /&gt;
| 1622-62-4&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Properties&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Solubility Solubility]&lt;br /&gt;
| Almost insoluble in water but soluble in alcohol&amp;lt;!--  at least put miscible with, not soluble in --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
&amp;lt;!-- | Other solvents e.g. [[ethanol]], [[acetone]] --&amp;gt;&lt;br /&gt;
&amp;lt;!-- | solubility info on other solvents --&amp;gt;&lt;br /&gt;
&amp;lt;!-- |- --&amp;gt;&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Melting_point Melting point]&lt;br /&gt;
| 168-172 C &amp;lt;!-- (mention any decomposition) --&amp;gt;&lt;br /&gt;
|}&lt;br /&gt;
===Rohypnol (Flunitrazepam) ===&lt;br /&gt;
&amp;lt;jmol&amp;gt;&lt;br /&gt;
&amp;lt;jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;size&amp;gt;200&amp;lt;/size&amp;gt;&lt;br /&gt;
&amp;lt;color&amp;gt;white&amp;lt;/color&amp;gt;&lt;br /&gt;
&amp;lt;script&amp;gt;zoom 80; cpk on;frame 1; move 10 -20 10 0 0 0 0 0 3; delay 1;&amp;lt;/script&amp;gt;&lt;br /&gt;
&amp;lt;inlineContents&amp;gt;Molecule-1&lt;br /&gt;
  WLViewer          3D                             0&lt;br /&gt;
&lt;br /&gt;
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   -1.7575    3.0755   -0.0128 C   0  0  0  0  0  0  0  0  0  1&lt;br /&gt;
   -1.6297    1.6014   -0.0031 N   0  0  0  0  0  0  0  0  0  2&lt;br /&gt;
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    2.0922    1.6398   -0.0497 C   0  0  0  0  0  0  0  0  0 11&lt;br /&gt;
   -2.0595   -1.6189    0.0233 N   0  0  0  0  0  0  0  0  0 12&lt;br /&gt;
   -0.1468   -3.1289    0.0744 C   0  0  0  0  0  0  0  0  0 13&lt;br /&gt;
    2.4132    0.3587   -0.0518 C   0  0  0  0  0  0  0  0  0 14&lt;br /&gt;
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    4.3160    0.9210   -0.0766 O   0  0  0  0  0  0  0  0  0 21&lt;br /&gt;
    3.5371   -1.2593   -0.0741 O   0  0  0  0  0  0  0  0  0 22&lt;br /&gt;
    0.9533   -5.7735    0.1176 C   0  0  0  0  0  0  0  0  0 23&lt;br /&gt;
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 17 22  2  0  0  0&lt;br /&gt;
 19 23  2  0  0  0&lt;br /&gt;
 20 23  1  0  0  0&lt;br /&gt;
M  END&lt;br /&gt;
title1&lt;br /&gt;
title2&lt;br /&gt;
&lt;br /&gt;
M  END&amp;lt;/inlineContents&amp;gt;&lt;br /&gt;
&amp;lt;/jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;/jmol&amp;gt;&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
Rohypnol is a sedative and belongs to a class of drugs known as the benzodiazepines which depress the central nervous system. It is the trade name for a compound known as flunitrazepam. The drug can be taken in a pill (1 and 2mg), crushed up and snorted or dissolved in a drink (alcohol). Rohypnol is manufactured worldwide for medical and therapeutic use but its popularity amongst drug users has rapidly increased and thus is referred to as a ‘Club Drug’ along with Ketamine, LSD and MDMA.&lt;br /&gt;
&lt;br /&gt;
==Synthesis==&lt;br /&gt;
&lt;br /&gt;
Flunitrazepam was first synthesised from (2-fluoro)-methylbenzene.&lt;br /&gt;
&lt;br /&gt;
==Mechanism of action==&lt;br /&gt;
&lt;br /&gt;
Rohypnol is lipophlic and when it is ingested, it is absorbed quickly into the bloodstream and enters the brain via oxidative pathways. The chemical is metabolised rapidly by enzymes (main one being CYP3A4) and binds to nerve receptors that are involved in co-ordination, memory and anxiety. In the absence of Rohypnol, the GABA neurotransmitter binds to these nerve receptors and reduces the activity in the brain. However, when Rohypnol is present it binds to another site (not the binding site) of GABA which slows down the nerve activity in the brain more efficiently. This enhancement of the GABA effect makes Rohypnol a ‘positive allosteric modulator’.&lt;br /&gt;
&lt;br /&gt;
As mentioned previously, Rohypnol is very rapidly absorbed and carried hepatically around the body and peak plasma concentrations occur after 40 minutes from ingestion and thus are a very fast acting benzodiazepine. In addition, Rohypnol has a long half life (roughly 18-26 hours) and a long lasting active metabolite so its effects can persist through to the next day. &lt;br /&gt;
&lt;br /&gt;
==Uses==&lt;br /&gt;
&lt;br /&gt;
Recreational&lt;br /&gt;
Rohypnol is grossly misused recreationally both on its own and with other drugs, e.g. with heroin to heighten the effects or after cocaine or methamphetamine use to ease the after effects of the high. It is also used to counteract the unwanted effects of stimulants such as paranoia, jitteriness, etc. It is used most frequently at raves and by high school and university students. Its low cost and availability is responsible for the rapidly growing numbers of Rohypnol users. &lt;br /&gt;
Medical&lt;br /&gt;
In the early 1970s, this drug was first used in hospitals where deep sedation was required. It is prescribed to relieve severe back pain and in the short term treatments of extreme cases of sleep disorders. It is also used therapeutically to calm patients. &lt;br /&gt;
&lt;br /&gt;
==Effects==&lt;br /&gt;
&lt;br /&gt;
As Rohypnol affects the neutosteroid metabolism, it interferes with brain and reproductive system functions. It results in changes to emotional state and motor functions. There are many short term effects from taking Rohypnol, the most common being amnesia. Others include: muscle relaxation, loss of inhibition, ‘drunken’ feeling, reduction in anxiety and hypnotic and euphoric effects. There are also adverse affects such as excessive sedation, impairment of balance and speech, lack of concentration, confusion, hallucinations, impaired psychomotor functions, slurred speech, and gastrointestinal distrurbances. Although it is classed as a depressant, in some individuals it may lead to aggressive behaviour or excitability. &lt;br /&gt;
&lt;br /&gt;
==Risks==&lt;br /&gt;
&lt;br /&gt;
It can be slipped into a drink unnoticed as it is odourless, tasteless and cannot be seen. There is therefore a high risk of a sexual assault and thus this drug is commonly known as the ‘date-rate drug’.&lt;br /&gt;
As the drug slows down the breathing and heart rate it can lead to breathing difficulties and nausea. The addictive nature of Rohypnol means that regular users are likely to develop a physical dependence. In addition, individuals may also develop a psychological dependence and overtime, increased doses are required to produce the same effect. Withdrawal effects are therefore inevitable and with heavy users, abrupt withdrawal can result in psychosis, seizures, severe insomnia and anxiety. When it is mixed with other drugs the adverse effects are heightened and the possibility of overdose is increased. Overdose can lead to excessive sedation, respiratory arrest which it most serious cases can result in coma and death. Comas and seizures are most likely when this sedative is combined with amphetamines.&lt;br /&gt;
When it is used during pregnancy, the lipolphilic Rohypnol penetrates the membranes and thus crosses over into the placenta resulting in a syndrome known as ‘Floppy Infant Syndrome’ when present in high doses.&lt;br /&gt;
&lt;br /&gt;
==Detection==&lt;br /&gt;
&lt;br /&gt;
Amnesia induced by taking this drug means that a victim of date-rape would not be able to provide any information about events that occurred whilst they were under its influence. This is the reason why the use of this drug in sexual assault is so common. The long half life of the drug means that sophisticated technological equipment can detect flunitrazepan and its related compounds in urine samples for up to about 5 days and roughly 30 days in hair.&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
! Mass Spectrum&lt;br /&gt;
&lt;br /&gt;
! Chromatogram&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
| [[Image:Mass Spec of Rohypnol png.PNG|thumb|Description]]&lt;br /&gt;
&lt;br /&gt;
| [[Image:Chromatogram of Flunitrazepam.PNG|thumb|Description]]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
==Legal status==&lt;br /&gt;
&lt;br /&gt;
Rohypnol is a class C drug. It is legal in 60 countries worldwide for medical use. It is available in the UK on private prescription otherwise its possession is illegal. Rohypnol is not legally available even for medical use in the US.&lt;br /&gt;
In 1998, the manufacturing company (Hoffman-Roche) improved the formula of the drug to make it easier to detect. It now contains a blue dye which appears when it is added to a drink and its solubility properties are altered such that it takes longer for it to dissolve into a drink. &lt;br /&gt;
&lt;br /&gt;
==Other names==&lt;br /&gt;
&lt;br /&gt;
Circles, Roach-2, Roofies, Roopies, Rope, R-2, Roaches, Forget-me-pills, Mexican Valium, Baptist Communion, R2-Do-U.&lt;br /&gt;
&lt;br /&gt;
==References==	&lt;br /&gt;
			&lt;br /&gt;
*http://128.255.99.21/publications/archive/hotline/1999/1999_06/rohypnol.xml&lt;/div&gt;</summary>
		<author><name>Wwl06</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=Rohypnol&amp;diff=13016</id>
		<title>Rohypnol</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=Rohypnol&amp;diff=13016"/>
		<updated>2007-12-05T11:34:30Z</updated>

		<summary type="html">&lt;p&gt;Wwl06: /* Detection */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&amp;lt;noinclude&amp;gt;&lt;br /&gt;
&amp;lt;!-- This template has been defined after elaborate discussion in the Chemicals Wikiproject. Please do not add, deleted or otherwise change it unless after due discussion in [[wikipedia talk:WikiProject Chemicals]] --&amp;gt;&lt;br /&gt;
&amp;lt;/noinclude&amp;gt;{| class=&amp;quot;toccolours&amp;quot; border=&amp;quot;1&amp;quot; style=&amp;quot;float: right; clear: right; margin: 0 0 1em 1em; border-collapse: collapse; width: 280px&amp;quot;&lt;br /&gt;
! {{chembox header}} | {{PAGENAME}} &amp;lt;!-- replace if not identical with the article name --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image:{{PAGENAME}}.jpg|200px|{{PAGENAME}}]] &amp;lt;!-- replace if not identical with the pagename --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | General&lt;br /&gt;
|- &lt;br /&gt;
| [http://en.wikipedia.org/wiki/IUPAC Systematic name]&lt;br /&gt;
| 6-(2-fluorophenyl)-2-methyl-9-nitro-2,&lt;br /&gt;
5-diazabicyclo[5.4.0]undeca-5,8,10,12-&lt;br /&gt;
tetraen-3-one&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Chemical_formula Molecular formula]&lt;br /&gt;
| C16H12FN3O3&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Molar_mass Molar mass]&lt;br /&gt;
| 313.3&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
| Appearance&lt;br /&gt;
| White, light yellow crystalline powder&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/CAS_registry_number CAS number]&lt;br /&gt;
| 1622-62-4&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Properties&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Solubility Solubility]&lt;br /&gt;
| Almost insoluble in water but soluble in alcohol&amp;lt;!--  at least put miscible with, not soluble in --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
&amp;lt;!-- | Other solvents e.g. [[ethanol]], [[acetone]] --&amp;gt;&lt;br /&gt;
&amp;lt;!-- | solubility info on other solvents --&amp;gt;&lt;br /&gt;
&amp;lt;!-- |- --&amp;gt;&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Melting_point Melting point]&lt;br /&gt;
| 168-172 C &amp;lt;!-- (mention any decomposition) --&amp;gt;&lt;br /&gt;
|}&lt;br /&gt;
===Rohypnol (Flunitrazepam) ===&lt;br /&gt;
&amp;lt;jmol&amp;gt;&lt;br /&gt;
&amp;lt;jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;size&amp;gt;200&amp;lt;/size&amp;gt;&lt;br /&gt;
&amp;lt;color&amp;gt;white&amp;lt;/color&amp;gt;&lt;br /&gt;
&amp;lt;script&amp;gt;zoom 80; cpk on;frame 1; move 10 -20 10 0 0 0 0 0 3; delay 1;&amp;lt;/script&amp;gt;&lt;br /&gt;
&amp;lt;inlineContents&amp;gt;Molecule-1&lt;br /&gt;
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&lt;br /&gt;
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&amp;lt;/jmol&amp;gt;&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
Rohypnol is a sedative and belongs to a class of drugs known as the benzodiazepines which depress the central nervous system. It is the trade name for a compound known as flunitrazepam. The drug can be taken in a pill (1 and 2mg), crushed up and snorted or dissolved in a drink (alcohol). Rohypnol is manufactured worldwide for medical and therapeutic use but its popularity amongst drug users has rapidly increased and thus is referred to as a ‘Club Drug’ along with Ketamine, LSD and MDMA.&lt;br /&gt;
&lt;br /&gt;
==Synthesis==&lt;br /&gt;
&lt;br /&gt;
Flunitrazepam was first synthesised from (2-fluoro)-methylbenzene.&lt;br /&gt;
&lt;br /&gt;
==Mechanism of action==&lt;br /&gt;
&lt;br /&gt;
Rohypnol is lipophlic and when it is ingested, it is absorbed quickly into the bloodstream and enters the brain via oxidative pathways. The chemical is metabolised rapidly by enzymes (main one being CYP3A4) and binds to nerve receptors that are involved in co-ordination, memory and anxiety. In the absence of Rohypnol, the GABA neurotransmitter binds to these nerve receptors and reduces the activity in the brain. However, when Rohypnol is present it binds to another site (not the binding site) of GABA which slows down the nerve activity in the brain more efficiently. This enhancement of the GABA effect makes Rohypnol a ‘positive allosteric modulator’.&lt;br /&gt;
&lt;br /&gt;
As mentioned previously, Rohypnol is very rapidly absorbed and carried hepatically around the body and peak plasma concentrations occur after 40 minutes from ingestion and thus are a very fast acting benzodiazepine. In addition, Rohypnol has a long half life (roughly 18-26 hours) and a long lasting active metabolite so its effects can persist through to the next day. &lt;br /&gt;
&lt;br /&gt;
==Uses==&lt;br /&gt;
&lt;br /&gt;
Recreational&lt;br /&gt;
Rohypnol is grossly misused recreationally both on its own and with other drugs, e.g. with heroin to heighten the effects or after cocaine or methamphetamine use to ease the after effects of the high. It is also used to counteract the unwanted effects of stimulants such as paranoia, jitteriness, etc. It is used most frequently at raves and by high school and university students. Its low cost and availability is responsible for the rapidly growing numbers of Rohypnol users. &lt;br /&gt;
Medical&lt;br /&gt;
In the early 1970s, this drug was first used in hospitals where deep sedation was required. It is prescribed to relieve severe back pain and in the short term treatments of extreme cases of sleep disorders. It is also used therapeutically to calm patients. &lt;br /&gt;
&lt;br /&gt;
==Effects==&lt;br /&gt;
&lt;br /&gt;
As Rohypnol affects the neutosteroid metabolism, it interferes with brain and reproductive system functions. It results in changes to emotional state and motor functions. There are many short term effects from taking Rohypnol, the most common being amnesia. Others include: muscle relaxation, loss of inhibition, ‘drunken’ feeling, reduction in anxiety and hypnotic and euphoric effects. There are also adverse affects such as excessive sedation, impairment of balance and speech, lack of concentration, confusion, hallucinations, impaired psychomotor functions, slurred speech, and gastrointestinal distrurbances. Although it is classed as a depressant, in some individuals it may lead to aggressive behaviour or excitability. &lt;br /&gt;
&lt;br /&gt;
==Risks==&lt;br /&gt;
&lt;br /&gt;
It can be slipped into a drink unnoticed as it is odourless, tasteless and cannot be seen. There is therefore a high risk of a sexual assault and thus this drug is commonly known as the ‘date-rate drug’.&lt;br /&gt;
As the drug slows down the breathing and heart rate it can lead to breathing difficulties and nausea. The addictive nature of Rohypnol means that regular users are likely to develop a physical dependence. In addition, individuals may also develop a psychological dependence and overtime, increased doses are required to produce the same effect. Withdrawal effects are therefore inevitable and with heavy users, abrupt withdrawal can result in psychosis, seizures, severe insomnia and anxiety. When it is mixed with other drugs the adverse effects are heightened and the possibility of overdose is increased. Overdose can lead to excessive sedation, respiratory arrest which it most serious cases can result in coma and death. Comas and seizures are most likely when this sedative is combined with amphetamines.&lt;br /&gt;
When it is used during pregnancy, the lipolphilic Rohypnol penetrates the membranes and thus crosses over into the placenta resulting in a syndrome known as ‘Floppy Infant Syndrome’ when present in high doses.&lt;br /&gt;
&lt;br /&gt;
==Detection==&lt;br /&gt;
&lt;br /&gt;
Amnesia induced by taking this drug means that a victim of date-rape would not be able to provide any information about events that occurred whilst they were under its influence. This is the reason why the use of this drug in sexual assault is so common. The long half life of the drug means that sophisticated technological equipment can detect flunitrazepan and its related compounds in urine samples for up to about 5 days and roughly 30 days in hair.&lt;br /&gt;
&lt;br /&gt;
Mass Spectrum&lt;br /&gt;
[[Image:Mass Spec of Rohypnol png.PNG|thumb|Description]]&lt;br /&gt;
&lt;br /&gt;
Chromatogram&lt;br /&gt;
[[Image:Chromatogram of Flunitrazepam.PNG|thumb|Description]]&lt;br /&gt;
&lt;br /&gt;
==Legal status==&lt;br /&gt;
&lt;br /&gt;
Rohypnol is a class C drug. It is legal in 60 countries worldwide for medical use. It is available in the UK on private prescription otherwise its possession is illegal. Rohypnol is not legally available even for medical use in the US.&lt;br /&gt;
In 1998, the manufacturing company (Hoffman-Roche) improved the formula of the drug to make it easier to detect. It now contains a blue dye which appears when it is added to a drink and its solubility properties are altered such that it takes longer for it to dissolve into a drink. &lt;br /&gt;
&lt;br /&gt;
==Other names==&lt;br /&gt;
&lt;br /&gt;
Circles, Roach-2, Roofies, Roopies, Rope, R-2, Roaches, Forget-me-pills, Mexican Valium, Baptist Communion, R2-Do-U.&lt;br /&gt;
&lt;br /&gt;
==References==	&lt;br /&gt;
			&lt;br /&gt;
*http://128.255.99.21/publications/archive/hotline/1999/1999_06/rohypnol.xml&lt;/div&gt;</summary>
		<author><name>Wwl06</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=File:Chromatogram_of_Flunitrazepam.PNG&amp;diff=13014</id>
		<title>File:Chromatogram of Flunitrazepam.PNG</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=File:Chromatogram_of_Flunitrazepam.PNG&amp;diff=13014"/>
		<updated>2007-12-05T11:33:32Z</updated>

		<summary type="html">&lt;p&gt;Wwl06: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;/div&gt;</summary>
		<author><name>Wwl06</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=Rohypnol&amp;diff=13010</id>
		<title>Rohypnol</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=Rohypnol&amp;diff=13010"/>
		<updated>2007-12-05T11:32:25Z</updated>

		<summary type="html">&lt;p&gt;Wwl06: /* Detection */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&amp;lt;noinclude&amp;gt;&lt;br /&gt;
&amp;lt;!-- This template has been defined after elaborate discussion in the Chemicals Wikiproject. Please do not add, deleted or otherwise change it unless after due discussion in [[wikipedia talk:WikiProject Chemicals]] --&amp;gt;&lt;br /&gt;
&amp;lt;/noinclude&amp;gt;{| class=&amp;quot;toccolours&amp;quot; border=&amp;quot;1&amp;quot; style=&amp;quot;float: right; clear: right; margin: 0 0 1em 1em; border-collapse: collapse; width: 280px&amp;quot;&lt;br /&gt;
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|-&lt;br /&gt;
! {{chembox header}} | General&lt;br /&gt;
|- &lt;br /&gt;
| [http://en.wikipedia.org/wiki/IUPAC Systematic name]&lt;br /&gt;
| 6-(2-fluorophenyl)-2-methyl-9-nitro-2,&lt;br /&gt;
5-diazabicyclo[5.4.0]undeca-5,8,10,12-&lt;br /&gt;
tetraen-3-one&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Chemical_formula Molecular formula]&lt;br /&gt;
| C16H12FN3O3&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Molar_mass Molar mass]&lt;br /&gt;
| 313.3&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
| Appearance&lt;br /&gt;
| White, light yellow crystalline powder&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/CAS_registry_number CAS number]&lt;br /&gt;
| 1622-62-4&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Properties&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Solubility Solubility]&lt;br /&gt;
| Almost insoluble in water but soluble in alcohol&amp;lt;!--  at least put miscible with, not soluble in --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
&amp;lt;!-- | Other solvents e.g. [[ethanol]], [[acetone]] --&amp;gt;&lt;br /&gt;
&amp;lt;!-- | solubility info on other solvents --&amp;gt;&lt;br /&gt;
&amp;lt;!-- |- --&amp;gt;&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Melting_point Melting point]&lt;br /&gt;
| 168-172 C &amp;lt;!-- (mention any decomposition) --&amp;gt;&lt;br /&gt;
|}&lt;br /&gt;
===Rohypnol (Flunitrazepam) ===&lt;br /&gt;
&amp;lt;jmol&amp;gt;&lt;br /&gt;
&amp;lt;jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;size&amp;gt;200&amp;lt;/size&amp;gt;&lt;br /&gt;
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&amp;lt;script&amp;gt;zoom 80; cpk on;frame 1; move 10 -20 10 0 0 0 0 0 3; delay 1;&amp;lt;/script&amp;gt;&lt;br /&gt;
&amp;lt;inlineContents&amp;gt;Molecule-1&lt;br /&gt;
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M  END&lt;br /&gt;
title1&lt;br /&gt;
title2&lt;br /&gt;
&lt;br /&gt;
M  END&amp;lt;/inlineContents&amp;gt;&lt;br /&gt;
&amp;lt;/jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;/jmol&amp;gt;&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
Rohypnol is a sedative and belongs to a class of drugs known as the benzodiazepines which depress the central nervous system. It is the trade name for a compound known as flunitrazepam. The drug can be taken in a pill (1 and 2mg), crushed up and snorted or dissolved in a drink (alcohol). Rohypnol is manufactured worldwide for medical and therapeutic use but its popularity amongst drug users has rapidly increased and thus is referred to as a ‘Club Drug’ along with Ketamine, LSD and MDMA.&lt;br /&gt;
&lt;br /&gt;
==Synthesis==&lt;br /&gt;
&lt;br /&gt;
Flunitrazepam was first synthesised from (2-fluoro)-methylbenzene.&lt;br /&gt;
&lt;br /&gt;
==Mechanism of action==&lt;br /&gt;
&lt;br /&gt;
Rohypnol is lipophlic and when it is ingested, it is absorbed quickly into the bloodstream and enters the brain via oxidative pathways. The chemical is metabolised rapidly by enzymes (main one being CYP3A4) and binds to nerve receptors that are involved in co-ordination, memory and anxiety. In the absence of Rohypnol, the GABA neurotransmitter binds to these nerve receptors and reduces the activity in the brain. However, when Rohypnol is present it binds to another site (not the binding site) of GABA which slows down the nerve activity in the brain more efficiently. This enhancement of the GABA effect makes Rohypnol a ‘positive allosteric modulator’.&lt;br /&gt;
&lt;br /&gt;
As mentioned previously, Rohypnol is very rapidly absorbed and carried hepatically around the body and peak plasma concentrations occur after 40 minutes from ingestion and thus are a very fast acting benzodiazepine. In addition, Rohypnol has a long half life (roughly 18-26 hours) and a long lasting active metabolite so its effects can persist through to the next day. &lt;br /&gt;
&lt;br /&gt;
==Uses==&lt;br /&gt;
&lt;br /&gt;
Recreational&lt;br /&gt;
Rohypnol is grossly misused recreationally both on its own and with other drugs, e.g. with heroin to heighten the effects or after cocaine or methamphetamine use to ease the after effects of the high. It is also used to counteract the unwanted effects of stimulants such as paranoia, jitteriness, etc. It is used most frequently at raves and by high school and university students. Its low cost and availability is responsible for the rapidly growing numbers of Rohypnol users. &lt;br /&gt;
Medical&lt;br /&gt;
In the early 1970s, this drug was first used in hospitals where deep sedation was required. It is prescribed to relieve severe back pain and in the short term treatments of extreme cases of sleep disorders. It is also used therapeutically to calm patients. &lt;br /&gt;
&lt;br /&gt;
==Effects==&lt;br /&gt;
&lt;br /&gt;
As Rohypnol affects the neutosteroid metabolism, it interferes with brain and reproductive system functions. It results in changes to emotional state and motor functions. There are many short term effects from taking Rohypnol, the most common being amnesia. Others include: muscle relaxation, loss of inhibition, ‘drunken’ feeling, reduction in anxiety and hypnotic and euphoric effects. There are also adverse affects such as excessive sedation, impairment of balance and speech, lack of concentration, confusion, hallucinations, impaired psychomotor functions, slurred speech, and gastrointestinal distrurbances. Although it is classed as a depressant, in some individuals it may lead to aggressive behaviour or excitability. &lt;br /&gt;
&lt;br /&gt;
==Risks==&lt;br /&gt;
&lt;br /&gt;
It can be slipped into a drink unnoticed as it is odourless, tasteless and cannot be seen. There is therefore a high risk of a sexual assault and thus this drug is commonly known as the ‘date-rate drug’.&lt;br /&gt;
As the drug slows down the breathing and heart rate it can lead to breathing difficulties and nausea. The addictive nature of Rohypnol means that regular users are likely to develop a physical dependence. In addition, individuals may also develop a psychological dependence and overtime, increased doses are required to produce the same effect. Withdrawal effects are therefore inevitable and with heavy users, abrupt withdrawal can result in psychosis, seizures, severe insomnia and anxiety. When it is mixed with other drugs the adverse effects are heightened and the possibility of overdose is increased. Overdose can lead to excessive sedation, respiratory arrest which it most serious cases can result in coma and death. Comas and seizures are most likely when this sedative is combined with amphetamines.&lt;br /&gt;
When it is used during pregnancy, the lipolphilic Rohypnol penetrates the membranes and thus crosses over into the placenta resulting in a syndrome known as ‘Floppy Infant Syndrome’ when present in high doses.&lt;br /&gt;
&lt;br /&gt;
==Detection==&lt;br /&gt;
&lt;br /&gt;
Amnesia induced by taking this drug means that a victim of date-rape would not be able to provide any information about events that occurred whilst they were under its influence. This is the reason why the use of this drug in sexual assault is so common. The long half life of the drug means that sophisticated technological equipment can detect flunitrazepan and its related compounds in urine samples for up to about 5 days and roughly 30 days in hair.&lt;br /&gt;
&lt;br /&gt;
[[Image:Mass Spec of Rohypnol png.PNG|thumb|Description]]&lt;br /&gt;
&lt;br /&gt;
==Legal status==&lt;br /&gt;
&lt;br /&gt;
Rohypnol is a class C drug. It is legal in 60 countries worldwide for medical use. It is available in the UK on private prescription otherwise its possession is illegal. Rohypnol is not legally available even for medical use in the US.&lt;br /&gt;
In 1998, the manufacturing company (Hoffman-Roche) improved the formula of the drug to make it easier to detect. It now contains a blue dye which appears when it is added to a drink and its solubility properties are altered such that it takes longer for it to dissolve into a drink. &lt;br /&gt;
&lt;br /&gt;
==Other names==&lt;br /&gt;
&lt;br /&gt;
Circles, Roach-2, Roofies, Roopies, Rope, R-2, Roaches, Forget-me-pills, Mexican Valium, Baptist Communion, R2-Do-U.&lt;br /&gt;
&lt;br /&gt;
==References==	&lt;br /&gt;
			&lt;br /&gt;
*http://128.255.99.21/publications/archive/hotline/1999/1999_06/rohypnol.xml&lt;/div&gt;</summary>
		<author><name>Wwl06</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=File:Mass_Spec_of_Rohypnol_png.PNG&amp;diff=13008</id>
		<title>File:Mass Spec of Rohypnol png.PNG</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=File:Mass_Spec_of_Rohypnol_png.PNG&amp;diff=13008"/>
		<updated>2007-12-05T11:31:43Z</updated>

		<summary type="html">&lt;p&gt;Wwl06: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;/div&gt;</summary>
		<author><name>Wwl06</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=Rohypnol&amp;diff=13004</id>
		<title>Rohypnol</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=Rohypnol&amp;diff=13004"/>
		<updated>2007-12-05T11:28:42Z</updated>

		<summary type="html">&lt;p&gt;Wwl06: /* Detection */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&amp;lt;noinclude&amp;gt;&lt;br /&gt;
&amp;lt;!-- This template has been defined after elaborate discussion in the Chemicals Wikiproject. Please do not add, deleted or otherwise change it unless after due discussion in [[wikipedia talk:WikiProject Chemicals]] --&amp;gt;&lt;br /&gt;
&amp;lt;/noinclude&amp;gt;{| class=&amp;quot;toccolours&amp;quot; border=&amp;quot;1&amp;quot; style=&amp;quot;float: right; clear: right; margin: 0 0 1em 1em; border-collapse: collapse; width: 280px&amp;quot;&lt;br /&gt;
! {{chembox header}} | {{PAGENAME}} &amp;lt;!-- replace if not identical with the article name --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image:{{PAGENAME}}.jpg|200px|{{PAGENAME}}]] &amp;lt;!-- replace if not identical with the pagename --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | General&lt;br /&gt;
|- &lt;br /&gt;
| [http://en.wikipedia.org/wiki/IUPAC Systematic name]&lt;br /&gt;
| 6-(2-fluorophenyl)-2-methyl-9-nitro-2,&lt;br /&gt;
5-diazabicyclo[5.4.0]undeca-5,8,10,12-&lt;br /&gt;
tetraen-3-one&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Chemical_formula Molecular formula]&lt;br /&gt;
| C16H12FN3O3&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Molar_mass Molar mass]&lt;br /&gt;
| 313.3&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
| Appearance&lt;br /&gt;
| White, light yellow crystalline powder&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/CAS_registry_number CAS number]&lt;br /&gt;
| 1622-62-4&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Properties&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Solubility Solubility]&lt;br /&gt;
| Almost insoluble in water but soluble in alcohol&amp;lt;!--  at least put miscible with, not soluble in --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
&amp;lt;!-- | Other solvents e.g. [[ethanol]], [[acetone]] --&amp;gt;&lt;br /&gt;
&amp;lt;!-- | solubility info on other solvents --&amp;gt;&lt;br /&gt;
&amp;lt;!-- |- --&amp;gt;&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Melting_point Melting point]&lt;br /&gt;
| 168-172 C &amp;lt;!-- (mention any decomposition) --&amp;gt;&lt;br /&gt;
|}&lt;br /&gt;
===Rohypnol (Flunitrazepam) ===&lt;br /&gt;
&amp;lt;jmol&amp;gt;&lt;br /&gt;
&amp;lt;jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;size&amp;gt;200&amp;lt;/size&amp;gt;&lt;br /&gt;
&amp;lt;color&amp;gt;white&amp;lt;/color&amp;gt;&lt;br /&gt;
&amp;lt;script&amp;gt;zoom 80; cpk on;frame 1; move 10 -20 10 0 0 0 0 0 3; delay 1;&amp;lt;/script&amp;gt;&lt;br /&gt;
&amp;lt;inlineContents&amp;gt;Molecule-1&lt;br /&gt;
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    0.9533   -5.7735    0.1176 C   0  0  0  0  0  0  0  0  0 23&lt;br /&gt;
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M  END&lt;br /&gt;
title1&lt;br /&gt;
title2&lt;br /&gt;
&lt;br /&gt;
M  END&amp;lt;/inlineContents&amp;gt;&lt;br /&gt;
&amp;lt;/jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;/jmol&amp;gt;&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
Rohypnol is a sedative and belongs to a class of drugs known as the benzodiazepines which depress the central nervous system. It is the trade name for a compound known as flunitrazepam. The drug can be taken in a pill (1 and 2mg), crushed up and snorted or dissolved in a drink (alcohol). Rohypnol is manufactured worldwide for medical and therapeutic use but its popularity amongst drug users has rapidly increased and thus is referred to as a ‘Club Drug’ along with Ketamine, LSD and MDMA.&lt;br /&gt;
&lt;br /&gt;
==Synthesis==&lt;br /&gt;
&lt;br /&gt;
Flunitrazepam was first synthesised from (2-fluoro)-methylbenzene.&lt;br /&gt;
&lt;br /&gt;
==Mechanism of action==&lt;br /&gt;
&lt;br /&gt;
Rohypnol is lipophlic and when it is ingested, it is absorbed quickly into the bloodstream and enters the brain via oxidative pathways. The chemical is metabolised rapidly by enzymes (main one being CYP3A4) and binds to nerve receptors that are involved in co-ordination, memory and anxiety. In the absence of Rohypnol, the GABA neurotransmitter binds to these nerve receptors and reduces the activity in the brain. However, when Rohypnol is present it binds to another site (not the binding site) of GABA which slows down the nerve activity in the brain more efficiently. This enhancement of the GABA effect makes Rohypnol a ‘positive allosteric modulator’.&lt;br /&gt;
&lt;br /&gt;
As mentioned previously, Rohypnol is very rapidly absorbed and carried hepatically around the body and peak plasma concentrations occur after 40 minutes from ingestion and thus are a very fast acting benzodiazepine. In addition, Rohypnol has a long half life (roughly 18-26 hours) and a long lasting active metabolite so its effects can persist through to the next day. &lt;br /&gt;
&lt;br /&gt;
==Uses==&lt;br /&gt;
&lt;br /&gt;
Recreational&lt;br /&gt;
Rohypnol is grossly misused recreationally both on its own and with other drugs, e.g. with heroin to heighten the effects or after cocaine or methamphetamine use to ease the after effects of the high. It is also used to counteract the unwanted effects of stimulants such as paranoia, jitteriness, etc. It is used most frequently at raves and by high school and university students. Its low cost and availability is responsible for the rapidly growing numbers of Rohypnol users. &lt;br /&gt;
Medical&lt;br /&gt;
In the early 1970s, this drug was first used in hospitals where deep sedation was required. It is prescribed to relieve severe back pain and in the short term treatments of extreme cases of sleep disorders. It is also used therapeutically to calm patients. &lt;br /&gt;
&lt;br /&gt;
==Effects==&lt;br /&gt;
&lt;br /&gt;
As Rohypnol affects the neutosteroid metabolism, it interferes with brain and reproductive system functions. It results in changes to emotional state and motor functions. There are many short term effects from taking Rohypnol, the most common being amnesia. Others include: muscle relaxation, loss of inhibition, ‘drunken’ feeling, reduction in anxiety and hypnotic and euphoric effects. There are also adverse affects such as excessive sedation, impairment of balance and speech, lack of concentration, confusion, hallucinations, impaired psychomotor functions, slurred speech, and gastrointestinal distrurbances. Although it is classed as a depressant, in some individuals it may lead to aggressive behaviour or excitability. &lt;br /&gt;
&lt;br /&gt;
==Risks==&lt;br /&gt;
&lt;br /&gt;
It can be slipped into a drink unnoticed as it is odourless, tasteless and cannot be seen. There is therefore a high risk of a sexual assault and thus this drug is commonly known as the ‘date-rate drug’.&lt;br /&gt;
As the drug slows down the breathing and heart rate it can lead to breathing difficulties and nausea. The addictive nature of Rohypnol means that regular users are likely to develop a physical dependence. In addition, individuals may also develop a psychological dependence and overtime, increased doses are required to produce the same effect. Withdrawal effects are therefore inevitable and with heavy users, abrupt withdrawal can result in psychosis, seizures, severe insomnia and anxiety. When it is mixed with other drugs the adverse effects are heightened and the possibility of overdose is increased. Overdose can lead to excessive sedation, respiratory arrest which it most serious cases can result in coma and death. Comas and seizures are most likely when this sedative is combined with amphetamines.&lt;br /&gt;
When it is used during pregnancy, the lipolphilic Rohypnol penetrates the membranes and thus crosses over into the placenta resulting in a syndrome known as ‘Floppy Infant Syndrome’ when present in high doses.&lt;br /&gt;
&lt;br /&gt;
==Detection==&lt;br /&gt;
&lt;br /&gt;
Amnesia induced by taking this drug means that a victim of date-rape would not be able to provide any information about events that occurred whilst they were under its influence. This is the reason why the use of this drug in sexual assault is so common. The long half life of the drug means that sophisticated technological equipment can detect flunitrazepan and its related compounds in urine samples for up to about 5 days and roughly 30 days in hair.&lt;br /&gt;
&lt;br /&gt;
[[Image:Mass Spec of Rohypnol.gif|thumb|Description]]&lt;br /&gt;
&lt;br /&gt;
==Legal status==&lt;br /&gt;
&lt;br /&gt;
Rohypnol is a class C drug. It is legal in 60 countries worldwide for medical use. It is available in the UK on private prescription otherwise its possession is illegal. Rohypnol is not legally available even for medical use in the US.&lt;br /&gt;
In 1998, the manufacturing company (Hoffman-Roche) improved the formula of the drug to make it easier to detect. It now contains a blue dye which appears when it is added to a drink and its solubility properties are altered such that it takes longer for it to dissolve into a drink. &lt;br /&gt;
&lt;br /&gt;
==Other names==&lt;br /&gt;
&lt;br /&gt;
Circles, Roach-2, Roofies, Roopies, Rope, R-2, Roaches, Forget-me-pills, Mexican Valium, Baptist Communion, R2-Do-U.&lt;br /&gt;
&lt;br /&gt;
==References==	&lt;br /&gt;
			&lt;br /&gt;
*http://128.255.99.21/publications/archive/hotline/1999/1999_06/rohypnol.xml&lt;/div&gt;</summary>
		<author><name>Wwl06</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=Rohypnol&amp;diff=13001</id>
		<title>Rohypnol</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=Rohypnol&amp;diff=13001"/>
		<updated>2007-12-05T11:26:36Z</updated>

		<summary type="html">&lt;p&gt;Wwl06: /* Detection */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&amp;lt;noinclude&amp;gt;&lt;br /&gt;
&amp;lt;!-- This template has been defined after elaborate discussion in the Chemicals Wikiproject. Please do not add, deleted or otherwise change it unless after due discussion in [[wikipedia talk:WikiProject Chemicals]] --&amp;gt;&lt;br /&gt;
&amp;lt;/noinclude&amp;gt;{| class=&amp;quot;toccolours&amp;quot; border=&amp;quot;1&amp;quot; style=&amp;quot;float: right; clear: right; margin: 0 0 1em 1em; border-collapse: collapse; width: 280px&amp;quot;&lt;br /&gt;
! {{chembox header}} | {{PAGENAME}} &amp;lt;!-- replace if not identical with the article name --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image:{{PAGENAME}}.jpg|200px|{{PAGENAME}}]] &amp;lt;!-- replace if not identical with the pagename --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | General&lt;br /&gt;
|- &lt;br /&gt;
| [http://en.wikipedia.org/wiki/IUPAC Systematic name]&lt;br /&gt;
| 6-(2-fluorophenyl)-2-methyl-9-nitro-2,&lt;br /&gt;
5-diazabicyclo[5.4.0]undeca-5,8,10,12-&lt;br /&gt;
tetraen-3-one&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Chemical_formula Molecular formula]&lt;br /&gt;
| C16H12FN3O3&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Molar_mass Molar mass]&lt;br /&gt;
| 313.3&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
| Appearance&lt;br /&gt;
| White, light yellow crystalline powder&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/CAS_registry_number CAS number]&lt;br /&gt;
| 1622-62-4&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Properties&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Solubility Solubility]&lt;br /&gt;
| Almost insoluble in water but soluble in alcohol&amp;lt;!--  at least put miscible with, not soluble in --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
&amp;lt;!-- | Other solvents e.g. [[ethanol]], [[acetone]] --&amp;gt;&lt;br /&gt;
&amp;lt;!-- | solubility info on other solvents --&amp;gt;&lt;br /&gt;
&amp;lt;!-- |- --&amp;gt;&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Melting_point Melting point]&lt;br /&gt;
| 168-172 C &amp;lt;!-- (mention any decomposition) --&amp;gt;&lt;br /&gt;
|}&lt;br /&gt;
===Rohypnol (Flunitrazepam) ===&lt;br /&gt;
&amp;lt;jmol&amp;gt;&lt;br /&gt;
&amp;lt;jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;size&amp;gt;200&amp;lt;/size&amp;gt;&lt;br /&gt;
&amp;lt;color&amp;gt;white&amp;lt;/color&amp;gt;&lt;br /&gt;
&amp;lt;script&amp;gt;zoom 80; cpk on;frame 1; move 10 -20 10 0 0 0 0 0 3; delay 1;&amp;lt;/script&amp;gt;&lt;br /&gt;
&amp;lt;inlineContents&amp;gt;Molecule-1&lt;br /&gt;
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&lt;br /&gt;
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    3.7354   -0.0966   -0.0725 N   0  0  0  0  0  0  0  0  0 17&lt;br /&gt;
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    0.9533   -5.7735    0.1176 C   0  0  0  0  0  0  0  0  0 23&lt;br /&gt;
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M  END&lt;br /&gt;
title1&lt;br /&gt;
title2&lt;br /&gt;
&lt;br /&gt;
M  END&amp;lt;/inlineContents&amp;gt;&lt;br /&gt;
&amp;lt;/jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;/jmol&amp;gt;&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
Rohypnol is a sedative and belongs to a class of drugs known as the benzodiazepines which depress the central nervous system. It is the trade name for a compound known as flunitrazepam. The drug can be taken in a pill (1 and 2mg), crushed up and snorted or dissolved in a drink (alcohol). Rohypnol is manufactured worldwide for medical and therapeutic use but its popularity amongst drug users has rapidly increased and thus is referred to as a ‘Club Drug’ along with Ketamine, LSD and MDMA.&lt;br /&gt;
&lt;br /&gt;
==Synthesis==&lt;br /&gt;
&lt;br /&gt;
Flunitrazepam was first synthesised from (2-fluoro)-methylbenzene.&lt;br /&gt;
&lt;br /&gt;
==Mechanism of action==&lt;br /&gt;
&lt;br /&gt;
Rohypnol is lipophlic and when it is ingested, it is absorbed quickly into the bloodstream and enters the brain via oxidative pathways. The chemical is metabolised rapidly by enzymes (main one being CYP3A4) and binds to nerve receptors that are involved in co-ordination, memory and anxiety. In the absence of Rohypnol, the GABA neurotransmitter binds to these nerve receptors and reduces the activity in the brain. However, when Rohypnol is present it binds to another site (not the binding site) of GABA which slows down the nerve activity in the brain more efficiently. This enhancement of the GABA effect makes Rohypnol a ‘positive allosteric modulator’.&lt;br /&gt;
&lt;br /&gt;
As mentioned previously, Rohypnol is very rapidly absorbed and carried hepatically around the body and peak plasma concentrations occur after 40 minutes from ingestion and thus are a very fast acting benzodiazepine. In addition, Rohypnol has a long half life (roughly 18-26 hours) and a long lasting active metabolite so its effects can persist through to the next day. &lt;br /&gt;
&lt;br /&gt;
==Uses==&lt;br /&gt;
&lt;br /&gt;
Recreational&lt;br /&gt;
Rohypnol is grossly misused recreationally both on its own and with other drugs, e.g. with heroin to heighten the effects or after cocaine or methamphetamine use to ease the after effects of the high. It is also used to counteract the unwanted effects of stimulants such as paranoia, jitteriness, etc. It is used most frequently at raves and by high school and university students. Its low cost and availability is responsible for the rapidly growing numbers of Rohypnol users. &lt;br /&gt;
Medical&lt;br /&gt;
In the early 1970s, this drug was first used in hospitals where deep sedation was required. It is prescribed to relieve severe back pain and in the short term treatments of extreme cases of sleep disorders. It is also used therapeutically to calm patients. &lt;br /&gt;
&lt;br /&gt;
==Effects==&lt;br /&gt;
&lt;br /&gt;
As Rohypnol affects the neutosteroid metabolism, it interferes with brain and reproductive system functions. It results in changes to emotional state and motor functions. There are many short term effects from taking Rohypnol, the most common being amnesia. Others include: muscle relaxation, loss of inhibition, ‘drunken’ feeling, reduction in anxiety and hypnotic and euphoric effects. There are also adverse affects such as excessive sedation, impairment of balance and speech, lack of concentration, confusion, hallucinations, impaired psychomotor functions, slurred speech, and gastrointestinal distrurbances. Although it is classed as a depressant, in some individuals it may lead to aggressive behaviour or excitability. &lt;br /&gt;
&lt;br /&gt;
==Risks==&lt;br /&gt;
&lt;br /&gt;
It can be slipped into a drink unnoticed as it is odourless, tasteless and cannot be seen. There is therefore a high risk of a sexual assault and thus this drug is commonly known as the ‘date-rate drug’.&lt;br /&gt;
As the drug slows down the breathing and heart rate it can lead to breathing difficulties and nausea. The addictive nature of Rohypnol means that regular users are likely to develop a physical dependence. In addition, individuals may also develop a psychological dependence and overtime, increased doses are required to produce the same effect. Withdrawal effects are therefore inevitable and with heavy users, abrupt withdrawal can result in psychosis, seizures, severe insomnia and anxiety. When it is mixed with other drugs the adverse effects are heightened and the possibility of overdose is increased. Overdose can lead to excessive sedation, respiratory arrest which it most serious cases can result in coma and death. Comas and seizures are most likely when this sedative is combined with amphetamines.&lt;br /&gt;
When it is used during pregnancy, the lipolphilic Rohypnol penetrates the membranes and thus crosses over into the placenta resulting in a syndrome known as ‘Floppy Infant Syndrome’ when present in high doses.&lt;br /&gt;
&lt;br /&gt;
==Detection==&lt;br /&gt;
&lt;br /&gt;
Amnesia induced by taking this drug means that a victim of date-rape would not be able to provide any information about events that occurred whilst they were under its influence. This is the reason why the use of this drug in sexual assault is so common. The long half life of the drug means that sophisticated technological equipment can detect flunitrazepan and its related compounds in urine samples for up to about 5 days and roughly 30 days in hair.&lt;br /&gt;
&lt;br /&gt;
==Legal status==&lt;br /&gt;
&lt;br /&gt;
Rohypnol is a class C drug. It is legal in 60 countries worldwide for medical use. It is available in the UK on private prescription otherwise its possession is illegal. Rohypnol is not legally available even for medical use in the US.&lt;br /&gt;
In 1998, the manufacturing company (Hoffman-Roche) improved the formula of the drug to make it easier to detect. It now contains a blue dye which appears when it is added to a drink and its solubility properties are altered such that it takes longer for it to dissolve into a drink. &lt;br /&gt;
&lt;br /&gt;
==Other names==&lt;br /&gt;
&lt;br /&gt;
Circles, Roach-2, Roofies, Roopies, Rope, R-2, Roaches, Forget-me-pills, Mexican Valium, Baptist Communion, R2-Do-U.&lt;br /&gt;
&lt;br /&gt;
==References==	&lt;br /&gt;
			&lt;br /&gt;
*http://128.255.99.21/publications/archive/hotline/1999/1999_06/rohypnol.xml&lt;/div&gt;</summary>
		<author><name>Wwl06</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=Rohypnol&amp;diff=12996</id>
		<title>Rohypnol</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=Rohypnol&amp;diff=12996"/>
		<updated>2007-12-05T11:25:02Z</updated>

		<summary type="html">&lt;p&gt;Wwl06: /* Detection */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&amp;lt;noinclude&amp;gt;&lt;br /&gt;
&amp;lt;!-- This template has been defined after elaborate discussion in the Chemicals Wikiproject. Please do not add, deleted or otherwise change it unless after due discussion in [[wikipedia talk:WikiProject Chemicals]] --&amp;gt;&lt;br /&gt;
&amp;lt;/noinclude&amp;gt;{| class=&amp;quot;toccolours&amp;quot; border=&amp;quot;1&amp;quot; style=&amp;quot;float: right; clear: right; margin: 0 0 1em 1em; border-collapse: collapse; width: 280px&amp;quot;&lt;br /&gt;
! {{chembox header}} | {{PAGENAME}} &amp;lt;!-- replace if not identical with the article name --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image:{{PAGENAME}}.jpg|200px|{{PAGENAME}}]] &amp;lt;!-- replace if not identical with the pagename --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | General&lt;br /&gt;
|- &lt;br /&gt;
| [http://en.wikipedia.org/wiki/IUPAC Systematic name]&lt;br /&gt;
| 6-(2-fluorophenyl)-2-methyl-9-nitro-2,&lt;br /&gt;
5-diazabicyclo[5.4.0]undeca-5,8,10,12-&lt;br /&gt;
tetraen-3-one&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Chemical_formula Molecular formula]&lt;br /&gt;
| C16H12FN3O3&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Molar_mass Molar mass]&lt;br /&gt;
| 313.3&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
| Appearance&lt;br /&gt;
| White, light yellow crystalline powder&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/CAS_registry_number CAS number]&lt;br /&gt;
| 1622-62-4&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Properties&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Solubility Solubility]&lt;br /&gt;
| Almost insoluble in water but soluble in alcohol&amp;lt;!--  at least put miscible with, not soluble in --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
&amp;lt;!-- | Other solvents e.g. [[ethanol]], [[acetone]] --&amp;gt;&lt;br /&gt;
&amp;lt;!-- | solubility info on other solvents --&amp;gt;&lt;br /&gt;
&amp;lt;!-- |- --&amp;gt;&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Melting_point Melting point]&lt;br /&gt;
| 168-172 C &amp;lt;!-- (mention any decomposition) --&amp;gt;&lt;br /&gt;
|}&lt;br /&gt;
===Rohypnol (Flunitrazepam) ===&lt;br /&gt;
&amp;lt;jmol&amp;gt;&lt;br /&gt;
&amp;lt;jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;size&amp;gt;200&amp;lt;/size&amp;gt;&lt;br /&gt;
&amp;lt;color&amp;gt;white&amp;lt;/color&amp;gt;&lt;br /&gt;
&amp;lt;script&amp;gt;zoom 80; cpk on;frame 1; move 10 -20 10 0 0 0 0 0 3; delay 1;&amp;lt;/script&amp;gt;&lt;br /&gt;
&amp;lt;inlineContents&amp;gt;Molecule-1&lt;br /&gt;
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&lt;br /&gt;
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M  END&lt;br /&gt;
title1&lt;br /&gt;
title2&lt;br /&gt;
&lt;br /&gt;
M  END&amp;lt;/inlineContents&amp;gt;&lt;br /&gt;
&amp;lt;/jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;/jmol&amp;gt;&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
Rohypnol is a sedative and belongs to a class of drugs known as the benzodiazepines which depress the central nervous system. It is the trade name for a compound known as flunitrazepam. The drug can be taken in a pill (1 and 2mg), crushed up and snorted or dissolved in a drink (alcohol). Rohypnol is manufactured worldwide for medical and therapeutic use but its popularity amongst drug users has rapidly increased and thus is referred to as a ‘Club Drug’ along with Ketamine, LSD and MDMA.&lt;br /&gt;
&lt;br /&gt;
==Synthesis==&lt;br /&gt;
&lt;br /&gt;
Flunitrazepam was first synthesised from (2-fluoro)-methylbenzene.&lt;br /&gt;
&lt;br /&gt;
==Mechanism of action==&lt;br /&gt;
&lt;br /&gt;
Rohypnol is lipophlic and when it is ingested, it is absorbed quickly into the bloodstream and enters the brain via oxidative pathways. The chemical is metabolised rapidly by enzymes (main one being CYP3A4) and binds to nerve receptors that are involved in co-ordination, memory and anxiety. In the absence of Rohypnol, the GABA neurotransmitter binds to these nerve receptors and reduces the activity in the brain. However, when Rohypnol is present it binds to another site (not the binding site) of GABA which slows down the nerve activity in the brain more efficiently. This enhancement of the GABA effect makes Rohypnol a ‘positive allosteric modulator’.&lt;br /&gt;
&lt;br /&gt;
As mentioned previously, Rohypnol is very rapidly absorbed and carried hepatically around the body and peak plasma concentrations occur after 40 minutes from ingestion and thus are a very fast acting benzodiazepine. In addition, Rohypnol has a long half life (roughly 18-26 hours) and a long lasting active metabolite so its effects can persist through to the next day. &lt;br /&gt;
&lt;br /&gt;
==Uses==&lt;br /&gt;
&lt;br /&gt;
Recreational&lt;br /&gt;
Rohypnol is grossly misused recreationally both on its own and with other drugs, e.g. with heroin to heighten the effects or after cocaine or methamphetamine use to ease the after effects of the high. It is also used to counteract the unwanted effects of stimulants such as paranoia, jitteriness, etc. It is used most frequently at raves and by high school and university students. Its low cost and availability is responsible for the rapidly growing numbers of Rohypnol users. &lt;br /&gt;
Medical&lt;br /&gt;
In the early 1970s, this drug was first used in hospitals where deep sedation was required. It is prescribed to relieve severe back pain and in the short term treatments of extreme cases of sleep disorders. It is also used therapeutically to calm patients. &lt;br /&gt;
&lt;br /&gt;
==Effects==&lt;br /&gt;
&lt;br /&gt;
As Rohypnol affects the neutosteroid metabolism, it interferes with brain and reproductive system functions. It results in changes to emotional state and motor functions. There are many short term effects from taking Rohypnol, the most common being amnesia. Others include: muscle relaxation, loss of inhibition, ‘drunken’ feeling, reduction in anxiety and hypnotic and euphoric effects. There are also adverse affects such as excessive sedation, impairment of balance and speech, lack of concentration, confusion, hallucinations, impaired psychomotor functions, slurred speech, and gastrointestinal distrurbances. Although it is classed as a depressant, in some individuals it may lead to aggressive behaviour or excitability. &lt;br /&gt;
&lt;br /&gt;
==Risks==&lt;br /&gt;
&lt;br /&gt;
It can be slipped into a drink unnoticed as it is odourless, tasteless and cannot be seen. There is therefore a high risk of a sexual assault and thus this drug is commonly known as the ‘date-rate drug’.&lt;br /&gt;
As the drug slows down the breathing and heart rate it can lead to breathing difficulties and nausea. The addictive nature of Rohypnol means that regular users are likely to develop a physical dependence. In addition, individuals may also develop a psychological dependence and overtime, increased doses are required to produce the same effect. Withdrawal effects are therefore inevitable and with heavy users, abrupt withdrawal can result in psychosis, seizures, severe insomnia and anxiety. When it is mixed with other drugs the adverse effects are heightened and the possibility of overdose is increased. Overdose can lead to excessive sedation, respiratory arrest which it most serious cases can result in coma and death. Comas and seizures are most likely when this sedative is combined with amphetamines.&lt;br /&gt;
When it is used during pregnancy, the lipolphilic Rohypnol penetrates the membranes and thus crosses over into the placenta resulting in a syndrome known as ‘Floppy Infant Syndrome’ when present in high doses.&lt;br /&gt;
&lt;br /&gt;
==Detection==&lt;br /&gt;
&lt;br /&gt;
Amnesia induced by taking this drug means that a victim of date-rape would not be able to provide any information about events that occurred whilst they were under its influence. This is the reason why the use of this drug in sexual assault is so common. The long half life of the drug means that sophisticated technological equipment can detect flunitrazepan and its related compounds in urine samples for up to about 5 days and roughly 30 days in hair.&lt;br /&gt;
&lt;br /&gt;
[[Image:Mass Spec of Rohypnol.gif|thumb|Description]]&lt;br /&gt;
&lt;br /&gt;
==Legal status==&lt;br /&gt;
&lt;br /&gt;
Rohypnol is a class C drug. It is legal in 60 countries worldwide for medical use. It is available in the UK on private prescription otherwise its possession is illegal. Rohypnol is not legally available even for medical use in the US.&lt;br /&gt;
In 1998, the manufacturing company (Hoffman-Roche) improved the formula of the drug to make it easier to detect. It now contains a blue dye which appears when it is added to a drink and its solubility properties are altered such that it takes longer for it to dissolve into a drink. &lt;br /&gt;
&lt;br /&gt;
==Other names==&lt;br /&gt;
&lt;br /&gt;
Circles, Roach-2, Roofies, Roopies, Rope, R-2, Roaches, Forget-me-pills, Mexican Valium, Baptist Communion, R2-Do-U.&lt;br /&gt;
&lt;br /&gt;
==References==	&lt;br /&gt;
			&lt;br /&gt;
*http://128.255.99.21/publications/archive/hotline/1999/1999_06/rohypnol.xml&lt;/div&gt;</summary>
		<author><name>Wwl06</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=File:Mass_Spec_of_Rohypnol.gif&amp;diff=12993</id>
		<title>File:Mass Spec of Rohypnol.gif</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=File:Mass_Spec_of_Rohypnol.gif&amp;diff=12993"/>
		<updated>2007-12-05T11:23:36Z</updated>

		<summary type="html">&lt;p&gt;Wwl06: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;/div&gt;</summary>
		<author><name>Wwl06</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=Rohypnol&amp;diff=12988</id>
		<title>Rohypnol</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=Rohypnol&amp;diff=12988"/>
		<updated>2007-12-05T11:18:32Z</updated>

		<summary type="html">&lt;p&gt;Wwl06: /* Risks */&lt;/p&gt;
&lt;hr /&gt;
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&amp;lt;!-- This template has been defined after elaborate discussion in the Chemicals Wikiproject. Please do not add, deleted or otherwise change it unless after due discussion in [[wikipedia talk:WikiProject Chemicals]] --&amp;gt;&lt;br /&gt;
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|-&lt;br /&gt;
! {{chembox header}} | General&lt;br /&gt;
|- &lt;br /&gt;
| [http://en.wikipedia.org/wiki/IUPAC Systematic name]&lt;br /&gt;
| 6-(2-fluorophenyl)-2-methyl-9-nitro-2,&lt;br /&gt;
5-diazabicyclo[5.4.0]undeca-5,8,10,12-&lt;br /&gt;
tetraen-3-one&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Chemical_formula Molecular formula]&lt;br /&gt;
| C16H12FN3O3&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Molar_mass Molar mass]&lt;br /&gt;
| 313.3&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
| Appearance&lt;br /&gt;
| White, light yellow crystalline powder&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/CAS_registry_number CAS number]&lt;br /&gt;
| 1622-62-4&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Properties&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Solubility Solubility]&lt;br /&gt;
| Almost insoluble in water but soluble in alcohol&amp;lt;!--  at least put miscible with, not soluble in --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
&amp;lt;!-- | Other solvents e.g. [[ethanol]], [[acetone]] --&amp;gt;&lt;br /&gt;
&amp;lt;!-- | solubility info on other solvents --&amp;gt;&lt;br /&gt;
&amp;lt;!-- |- --&amp;gt;&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Melting_point Melting point]&lt;br /&gt;
| 168-172 C &amp;lt;!-- (mention any decomposition) --&amp;gt;&lt;br /&gt;
|}&lt;br /&gt;
===Rohypnol (Flunitrazepam) ===&lt;br /&gt;
&amp;lt;jmol&amp;gt;&lt;br /&gt;
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&lt;br /&gt;
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Rohypnol is a sedative and belongs to a class of drugs known as the benzodiazepines which depress the central nervous system. It is the trade name for a compound known as flunitrazepam. The drug can be taken in a pill (1 and 2mg), crushed up and snorted or dissolved in a drink (alcohol). Rohypnol is manufactured worldwide for medical and therapeutic use but its popularity amongst drug users has rapidly increased and thus is referred to as a ‘Club Drug’ along with Ketamine, LSD and MDMA.&lt;br /&gt;
&lt;br /&gt;
==Synthesis==&lt;br /&gt;
&lt;br /&gt;
Flunitrazepam was first synthesised from (2-fluoro)-methylbenzene.&lt;br /&gt;
&lt;br /&gt;
==Mechanism of action==&lt;br /&gt;
&lt;br /&gt;
Rohypnol is lipophlic and when it is ingested, it is absorbed quickly into the bloodstream and enters the brain via oxidative pathways. The chemical is metabolised rapidly by enzymes (main one being CYP3A4) and binds to nerve receptors that are involved in co-ordination, memory and anxiety. In the absence of Rohypnol, the GABA neurotransmitter binds to these nerve receptors and reduces the activity in the brain. However, when Rohypnol is present it binds to another site (not the binding site) of GABA which slows down the nerve activity in the brain more efficiently. This enhancement of the GABA effect makes Rohypnol a ‘positive allosteric modulator’.&lt;br /&gt;
&lt;br /&gt;
As mentioned previously, Rohypnol is very rapidly absorbed and carried hepatically around the body and peak plasma concentrations occur after 40 minutes from ingestion and thus are a very fast acting benzodiazepine. In addition, Rohypnol has a long half life (roughly 18-26 hours) and a long lasting active metabolite so its effects can persist through to the next day. &lt;br /&gt;
&lt;br /&gt;
==Uses==&lt;br /&gt;
&lt;br /&gt;
Recreational&lt;br /&gt;
Rohypnol is grossly misused recreationally both on its own and with other drugs, e.g. with heroin to heighten the effects or after cocaine or methamphetamine use to ease the after effects of the high. It is also used to counteract the unwanted effects of stimulants such as paranoia, jitteriness, etc. It is used most frequently at raves and by high school and university students. Its low cost and availability is responsible for the rapidly growing numbers of Rohypnol users. &lt;br /&gt;
Medical&lt;br /&gt;
In the early 1970s, this drug was first used in hospitals where deep sedation was required. It is prescribed to relieve severe back pain and in the short term treatments of extreme cases of sleep disorders. It is also used therapeutically to calm patients. &lt;br /&gt;
&lt;br /&gt;
==Effects==&lt;br /&gt;
&lt;br /&gt;
As Rohypnol affects the neutosteroid metabolism, it interferes with brain and reproductive system functions. It results in changes to emotional state and motor functions. There are many short term effects from taking Rohypnol, the most common being amnesia. Others include: muscle relaxation, loss of inhibition, ‘drunken’ feeling, reduction in anxiety and hypnotic and euphoric effects. There are also adverse affects such as excessive sedation, impairment of balance and speech, lack of concentration, confusion, hallucinations, impaired psychomotor functions, slurred speech, and gastrointestinal distrurbances. Although it is classed as a depressant, in some individuals it may lead to aggressive behaviour or excitability. &lt;br /&gt;
&lt;br /&gt;
==Risks==&lt;br /&gt;
&lt;br /&gt;
It can be slipped into a drink unnoticed as it is odourless, tasteless and cannot be seen. There is therefore a high risk of a sexual assault and thus this drug is commonly known as the ‘date-rate drug’.&lt;br /&gt;
As the drug slows down the breathing and heart rate it can lead to breathing difficulties and nausea. The addictive nature of Rohypnol means that regular users are likely to develop a physical dependence. In addition, individuals may also develop a psychological dependence and overtime, increased doses are required to produce the same effect. Withdrawal effects are therefore inevitable and with heavy users, abrupt withdrawal can result in psychosis, seizures, severe insomnia and anxiety. When it is mixed with other drugs the adverse effects are heightened and the possibility of overdose is increased. Overdose can lead to excessive sedation, respiratory arrest which it most serious cases can result in coma and death. Comas and seizures are most likely when this sedative is combined with amphetamines.&lt;br /&gt;
When it is used during pregnancy, the lipolphilic Rohypnol penetrates the membranes and thus crosses over into the placenta resulting in a syndrome known as ‘Floppy Infant Syndrome’ when present in high doses.&lt;br /&gt;
&lt;br /&gt;
==Detection==&lt;br /&gt;
&lt;br /&gt;
Amnesia induced by taking this drug means that a victim of date-rape would not be able to provide any information about events that occurred whilst they were under its influence. This is the reason why the use of this drug in sexual assault is so common. The long half life of the drug means that sophisticated technological equipment can detect flunitrazepan and its related compounds in urine samples for up to about 5 days and roughly 30 days in hair.&lt;br /&gt;
&lt;br /&gt;
==Legal status==&lt;br /&gt;
&lt;br /&gt;
Rohypnol is a class C drug. It is legal in 60 countries worldwide for medical use. It is available in the UK on private prescription otherwise its possession is illegal. Rohypnol is not legally available even for medical use in the US.&lt;br /&gt;
In 1998, the manufacturing company (Hoffman-Roche) improved the formula of the drug to make it easier to detect. It now contains a blue dye which appears when it is added to a drink and its solubility properties are altered such that it takes longer for it to dissolve into a drink. &lt;br /&gt;
&lt;br /&gt;
==Other names==&lt;br /&gt;
&lt;br /&gt;
Circles, Roach-2, Roofies, Roopies, Rope, R-2, Roaches, Forget-me-pills, Mexican Valium, Baptist Communion, R2-Do-U.&lt;br /&gt;
&lt;br /&gt;
==References==	&lt;br /&gt;
			&lt;br /&gt;
*http://128.255.99.21/publications/archive/hotline/1999/1999_06/rohypnol.xml&lt;/div&gt;</summary>
		<author><name>Wwl06</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=Rohypnol&amp;diff=12646</id>
		<title>Rohypnol</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=Rohypnol&amp;diff=12646"/>
		<updated>2007-12-03T14:16:18Z</updated>

		<summary type="html">&lt;p&gt;Wwl06: /* Other names */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&amp;lt;noinclude&amp;gt;&lt;br /&gt;
&amp;lt;!-- This template has been defined after elaborate discussion in the Chemicals Wikiproject. Please do not add, deleted or otherwise change it unless after due discussion in [[wikipedia talk:WikiProject Chemicals]] --&amp;gt;&lt;br /&gt;
&amp;lt;/noinclude&amp;gt;{| class=&amp;quot;toccolours&amp;quot; border=&amp;quot;1&amp;quot; style=&amp;quot;float: right; clear: right; margin: 0 0 1em 1em; border-collapse: collapse; width: 280px&amp;quot;&lt;br /&gt;
! {{chembox header}} | {{PAGENAME}} &amp;lt;!-- replace if not identical with the article name --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image:{{PAGENAME}}.jpg|200px|{{PAGENAME}}]] &amp;lt;!-- replace if not identical with the pagename --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | General&lt;br /&gt;
|- &lt;br /&gt;
| [http://en.wikipedia.org/wiki/IUPAC Systematic name]&lt;br /&gt;
| 6-(2-fluorophenyl)-2-methyl-9-nitro-2,&lt;br /&gt;
5-diazabicyclo[5.4.0]undeca-5,8,10,12-&lt;br /&gt;
tetraen-3-one&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Chemical_formula Molecular formula]&lt;br /&gt;
| C16H12FN3O3&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Molar_mass Molar mass]&lt;br /&gt;
| 313.3&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
| Appearance&lt;br /&gt;
| White, light yellow crystalline powder&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/CAS_registry_number CAS number]&lt;br /&gt;
| 1622-62-4&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Properties&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Solubility Solubility]&lt;br /&gt;
| Almost insoluble in water but soluble in alcohol&amp;lt;!--  at least put miscible with, not soluble in --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
&amp;lt;!-- | Other solvents e.g. [[ethanol]], [[acetone]] --&amp;gt;&lt;br /&gt;
&amp;lt;!-- | solubility info on other solvents --&amp;gt;&lt;br /&gt;
&amp;lt;!-- |- --&amp;gt;&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Melting_point Melting point]&lt;br /&gt;
| 168-172 C &amp;lt;!-- (mention any decomposition) --&amp;gt;&lt;br /&gt;
|}&lt;br /&gt;
===Rohypnol (Flunitrazepam) ===&lt;br /&gt;
&amp;lt;jmol&amp;gt;&lt;br /&gt;
&amp;lt;jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;size&amp;gt;200&amp;lt;/size&amp;gt;&lt;br /&gt;
&amp;lt;color&amp;gt;white&amp;lt;/color&amp;gt;&lt;br /&gt;
&amp;lt;script&amp;gt;zoom 80; cpk on;frame 1; move 10 -20 10 0 0 0 0 0 3; delay 1;&amp;lt;/script&amp;gt;&lt;br /&gt;
&amp;lt;inlineContents&amp;gt;Molecule-1&lt;br /&gt;
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title2&lt;br /&gt;
&lt;br /&gt;
M  END&amp;lt;/inlineContents&amp;gt;&lt;br /&gt;
&amp;lt;/jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;/jmol&amp;gt;&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
Rohypnol is a sedative and belongs to a class of drugs known as the benzodiazepines which depress the central nervous system. It is the trade name for a compound known as flunitrazepam. The drug can be taken in a pill (1 and 2mg), crushed up and snorted or dissolved in a drink (alcohol). Rohypnol is manufactured worldwide for medical and therapeutic use but its popularity amongst drug users has rapidly increased and thus is referred to as a ‘Club Drug’ along with Ketamine, LSD and MDMA.&lt;br /&gt;
&lt;br /&gt;
==Synthesis==&lt;br /&gt;
&lt;br /&gt;
Flunitrazepam was first synthesised from (2-fluoro)-methylbenzene.&lt;br /&gt;
&lt;br /&gt;
==Mechanism of action==&lt;br /&gt;
&lt;br /&gt;
Rohypnol is lipophlic and when it is ingested, it is absorbed quickly into the bloodstream and enters the brain via oxidative pathways. The chemical is metabolised rapidly by enzymes (main one being CYP3A4) and binds to nerve receptors that are involved in co-ordination, memory and anxiety. In the absence of Rohypnol, the GABA neurotransmitter binds to these nerve receptors and reduces the activity in the brain. However, when Rohypnol is present it binds to another site (not the binding site) of GABA which slows down the nerve activity in the brain more efficiently. This enhancement of the GABA effect makes Rohypnol a ‘positive allosteric modulator’.&lt;br /&gt;
&lt;br /&gt;
As mentioned previously, Rohypnol is very rapidly absorbed and carried hepatically around the body and peak plasma concentrations occur after 40 minutes from ingestion and thus are a very fast acting benzodiazepine. In addition, Rohypnol has a long half life (roughly 18-26 hours) and a long lasting active metabolite so its effects can persist through to the next day. &lt;br /&gt;
&lt;br /&gt;
==Uses==&lt;br /&gt;
&lt;br /&gt;
Recreational&lt;br /&gt;
Rohypnol is grossly misused recreationally both on its own and with other drugs, e.g. with heroin to heighten the effects or after cocaine or methamphetamine use to ease the after effects of the high. It is also used to counteract the unwanted effects of stimulants such as paranoia, jitteriness, etc. It is used most frequently at raves and by high school and university students. Its low cost and availability is responsible for the rapidly growing numbers of Rohypnol users. &lt;br /&gt;
Medical&lt;br /&gt;
In the early 1970s, this drug was first used in hospitals where deep sedation was required. It is prescribed to relieve severe back pain and in the short term treatments of extreme cases of sleep disorders. It is also used therapeutically to calm patients. &lt;br /&gt;
&lt;br /&gt;
==Effects==&lt;br /&gt;
&lt;br /&gt;
As Rohypnol affects the neutosteroid metabolism, it interferes with brain and reproductive system functions. It results in changes to emotional state and motor functions. There are many short term effects from taking Rohypnol, the most common being amnesia. Others include: muscle relaxation, loss of inhibition, ‘drunken’ feeling, reduction in anxiety and hypnotic and euphoric effects. There are also adverse affects such as excessive sedation, impairment of balance and speech, lack of concentration, confusion, hallucinations, impaired psychomotor functions, slurred speech, and gastrointestinal distrurbances. Although it is classed as a depressant, in some individuals it may lead to aggressive behaviour or excitability. &lt;br /&gt;
&lt;br /&gt;
==Risks==&lt;br /&gt;
&lt;br /&gt;
It can be slipped into a drink unnoticed as it is odourless, tasteless and cannot be seen. There is therefore a high risk of a sexual assault and thus this drug is commonly known as the ‘date-rate drug’.&lt;br /&gt;
As the drug slows down the breathing and heart rate it can lead to breathing difficulties and nausea. The addictive nature of Rohypnol means that regular users are likely to develop a physical dependence. In addition, individuals may also develop a psychological dependence and overtime, increased doses are required to produce the same effect. Withdrawal effects are therefore inevitable and with heavy users, abrupt withdrawal can result in psychosis, seizures, severe insomnia and anxiety. When it is mixed with other drugs the adverse effects are heightened and the possibility of overdose is increased. Overdose can lead to excessive sedation, respiratory arrest which it most serious cases can result in coma and death. Comas and seizures are most likely when this sedative is combined with amphetamines.&lt;br /&gt;
When it is used during pregnancy, the lipolphilic Rohypnol penetrates the membranes and thus crosses over into the placenta resulting in a syndrome known as ‘Floppy Infant Syndrome’ when present in high doses.&lt;br /&gt;
&lt;br /&gt;
==Legal status==&lt;br /&gt;
&lt;br /&gt;
Rohypnol is a class C drug. It is legal in 60 countries worldwide for medical use. It is available in the UK on private prescription otherwise its possession is illegal. Rohypnol is not legally available even for medical use in the US.&lt;br /&gt;
In 1998, the manufacturing company (Hoffman-Roche) improved the formula of the drug to make it easier to detect. It now contains a blue dye which appears when it is added to a drink and its solubility properties are altered such that it takes longer for it to dissolve into a drink. &lt;br /&gt;
&lt;br /&gt;
==Other names==&lt;br /&gt;
&lt;br /&gt;
Circles, Roach-2, Roofies, Roopies, Rope, R-2, Roaches, Forget-me-pills, Mexican Valium, Baptist Communion, R2-Do-U.&lt;br /&gt;
&lt;br /&gt;
==References==	&lt;br /&gt;
			&lt;br /&gt;
*http://128.255.99.21/publications/archive/hotline/1999/1999_06/rohypnol.xml&lt;/div&gt;</summary>
		<author><name>Wwl06</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=Rohypnol&amp;diff=12645</id>
		<title>Rohypnol</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=Rohypnol&amp;diff=12645"/>
		<updated>2007-12-03T14:10:42Z</updated>

		<summary type="html">&lt;p&gt;Wwl06: /* Rohypnol (Flunitrazepam) */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&amp;lt;noinclude&amp;gt;&lt;br /&gt;
&amp;lt;!-- This template has been defined after elaborate discussion in the Chemicals Wikiproject. Please do not add, deleted or otherwise change it unless after due discussion in [[wikipedia talk:WikiProject Chemicals]] --&amp;gt;&lt;br /&gt;
&amp;lt;/noinclude&amp;gt;{| class=&amp;quot;toccolours&amp;quot; border=&amp;quot;1&amp;quot; style=&amp;quot;float: right; clear: right; margin: 0 0 1em 1em; border-collapse: collapse; width: 280px&amp;quot;&lt;br /&gt;
! {{chembox header}} | {{PAGENAME}} &amp;lt;!-- replace if not identical with the article name --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image:{{PAGENAME}}.jpg|200px|{{PAGENAME}}]] &amp;lt;!-- replace if not identical with the pagename --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | General&lt;br /&gt;
|- &lt;br /&gt;
| [http://en.wikipedia.org/wiki/IUPAC Systematic name]&lt;br /&gt;
| 6-(2-fluorophenyl)-2-methyl-9-nitro-2,&lt;br /&gt;
5-diazabicyclo[5.4.0]undeca-5,8,10,12-&lt;br /&gt;
tetraen-3-one&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Chemical_formula Molecular formula]&lt;br /&gt;
| C16H12FN3O3&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Molar_mass Molar mass]&lt;br /&gt;
| 313.3&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
| Appearance&lt;br /&gt;
| White, light yellow crystalline powder&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/CAS_registry_number CAS number]&lt;br /&gt;
| 1622-62-4&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Properties&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Solubility Solubility]&lt;br /&gt;
| Almost insoluble in water but soluble in alcohol&amp;lt;!--  at least put miscible with, not soluble in --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
&amp;lt;!-- | Other solvents e.g. [[ethanol]], [[acetone]] --&amp;gt;&lt;br /&gt;
&amp;lt;!-- | solubility info on other solvents --&amp;gt;&lt;br /&gt;
&amp;lt;!-- |- --&amp;gt;&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Melting_point Melting point]&lt;br /&gt;
| 168-172 C &amp;lt;!-- (mention any decomposition) --&amp;gt;&lt;br /&gt;
|}&lt;br /&gt;
===Rohypnol (Flunitrazepam) ===&lt;br /&gt;
&amp;lt;jmol&amp;gt;&lt;br /&gt;
&amp;lt;jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;size&amp;gt;200&amp;lt;/size&amp;gt;&lt;br /&gt;
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&amp;lt;script&amp;gt;zoom 80; cpk on;frame 1; move 10 -20 10 0 0 0 0 0 3; delay 1;&amp;lt;/script&amp;gt;&lt;br /&gt;
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    0.9533   -5.7735    0.1176 C   0  0  0  0  0  0  0  0  0 23&lt;br /&gt;
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M  END&lt;br /&gt;
title1&lt;br /&gt;
title2&lt;br /&gt;
&lt;br /&gt;
M  END&amp;lt;/inlineContents&amp;gt;&lt;br /&gt;
&amp;lt;/jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;/jmol&amp;gt;&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
Rohypnol is a sedative and belongs to a class of drugs known as the benzodiazepines which depress the central nervous system. It is the trade name for a compound known as flunitrazepam. The drug can be taken in a pill (1 and 2mg), crushed up and snorted or dissolved in a drink (alcohol). Rohypnol is manufactured worldwide for medical and therapeutic use but its popularity amongst drug users has rapidly increased and thus is referred to as a ‘Club Drug’ along with Ketamine, LSD and MDMA.&lt;br /&gt;
&lt;br /&gt;
==Synthesis==&lt;br /&gt;
&lt;br /&gt;
Flunitrazepam was first synthesised from (2-fluoro)-methylbenzene.&lt;br /&gt;
&lt;br /&gt;
==Mechanism of action==&lt;br /&gt;
&lt;br /&gt;
Rohypnol is lipophlic and when it is ingested, it is absorbed quickly into the bloodstream and enters the brain via oxidative pathways. The chemical is metabolised rapidly by enzymes (main one being CYP3A4) and binds to nerve receptors that are involved in co-ordination, memory and anxiety. In the absence of Rohypnol, the GABA neurotransmitter binds to these nerve receptors and reduces the activity in the brain. However, when Rohypnol is present it binds to another site (not the binding site) of GABA which slows down the nerve activity in the brain more efficiently. This enhancement of the GABA effect makes Rohypnol a ‘positive allosteric modulator’.&lt;br /&gt;
&lt;br /&gt;
As mentioned previously, Rohypnol is very rapidly absorbed and carried hepatically around the body and peak plasma concentrations occur after 40 minutes from ingestion and thus are a very fast acting benzodiazepine. In addition, Rohypnol has a long half life (roughly 18-26 hours) and a long lasting active metabolite so its effects can persist through to the next day. &lt;br /&gt;
&lt;br /&gt;
==Uses==&lt;br /&gt;
&lt;br /&gt;
Recreational&lt;br /&gt;
Rohypnol is grossly misused recreationally both on its own and with other drugs, e.g. with heroin to heighten the effects or after cocaine or methamphetamine use to ease the after effects of the high. It is also used to counteract the unwanted effects of stimulants such as paranoia, jitteriness, etc. It is used most frequently at raves and by high school and university students. Its low cost and availability is responsible for the rapidly growing numbers of Rohypnol users. &lt;br /&gt;
Medical&lt;br /&gt;
In the early 1970s, this drug was first used in hospitals where deep sedation was required. It is prescribed to relieve severe back pain and in the short term treatments of extreme cases of sleep disorders. It is also used therapeutically to calm patients. &lt;br /&gt;
&lt;br /&gt;
==Effects==&lt;br /&gt;
&lt;br /&gt;
As Rohypnol affects the neutosteroid metabolism, it interferes with brain and reproductive system functions. It results in changes to emotional state and motor functions. There are many short term effects from taking Rohypnol, the most common being amnesia. Others include: muscle relaxation, loss of inhibition, ‘drunken’ feeling, reduction in anxiety and hypnotic and euphoric effects. There are also adverse affects such as excessive sedation, impairment of balance and speech, lack of concentration, confusion, hallucinations, impaired psychomotor functions, slurred speech, and gastrointestinal distrurbances. Although it is classed as a depressant, in some individuals it may lead to aggressive behaviour or excitability. &lt;br /&gt;
&lt;br /&gt;
==Risks==&lt;br /&gt;
&lt;br /&gt;
It can be slipped into a drink unnoticed as it is odourless, tasteless and cannot be seen. There is therefore a high risk of a sexual assault and thus this drug is commonly known as the ‘date-rate drug’.&lt;br /&gt;
As the drug slows down the breathing and heart rate it can lead to breathing difficulties and nausea. The addictive nature of Rohypnol means that regular users are likely to develop a physical dependence. In addition, individuals may also develop a psychological dependence and overtime, increased doses are required to produce the same effect. Withdrawal effects are therefore inevitable and with heavy users, abrupt withdrawal can result in psychosis, seizures, severe insomnia and anxiety. When it is mixed with other drugs the adverse effects are heightened and the possibility of overdose is increased. Overdose can lead to excessive sedation, respiratory arrest which it most serious cases can result in coma and death. Comas and seizures are most likely when this sedative is combined with amphetamines.&lt;br /&gt;
When it is used during pregnancy, the lipolphilic Rohypnol penetrates the membranes and thus crosses over into the placenta resulting in a syndrome known as ‘Floppy Infant Syndrome’ when present in high doses.&lt;br /&gt;
&lt;br /&gt;
==Legal status==&lt;br /&gt;
&lt;br /&gt;
Rohypnol is a class C drug. It is legal in 60 countries worldwide for medical use. It is available in the UK on private prescription otherwise its possession is illegal. Rohypnol is not legally available even for medical use in the US.&lt;br /&gt;
In 1998, the manufacturing company (Hoffman-Roche) improved the formula of the drug to make it easier to detect. It now contains a blue dye which appears when it is added to a drink and its solubility properties are altered such that it takes longer for it to dissolve into a drink. &lt;br /&gt;
&lt;br /&gt;
==Other names==&lt;br /&gt;
&lt;br /&gt;
Circles, Roach-2, Roofies, Roopies, Rope, R-2, Roaches, Forget-me-pills, Mexican Valium, Baptist Communion, R2-Do-U.&lt;/div&gt;</summary>
		<author><name>Wwl06</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=Rohypnol&amp;diff=12101</id>
		<title>Rohypnol</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=Rohypnol&amp;diff=12101"/>
		<updated>2007-11-27T16:29:26Z</updated>

		<summary type="html">&lt;p&gt;Wwl06: /* Rohypnol (Flunitrazepam) */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&amp;lt;noinclude&amp;gt;&lt;br /&gt;
&amp;lt;!-- This template has been defined after elaborate discussion in the Chemicals Wikiproject. Please do not add, deleted or otherwise change it unless after due discussion in [[wikipedia talk:WikiProject Chemicals]] --&amp;gt;&lt;br /&gt;
&amp;lt;/noinclude&amp;gt;{| class=&amp;quot;toccolours&amp;quot; border=&amp;quot;1&amp;quot; style=&amp;quot;float: right; clear: right; margin: 0 0 1em 1em; border-collapse: collapse; width: 280px&amp;quot;&lt;br /&gt;
! {{chembox header}} | {{PAGENAME}} &amp;lt;!-- replace if not identical with the article name --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image:{{PAGENAME}}.jpg|200px|{{PAGENAME}}]] &amp;lt;!-- replace if not identical with the pagename --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | General&lt;br /&gt;
|- &lt;br /&gt;
| [http://en.wikipedia.org/wiki/IUPAC Systematic name]&lt;br /&gt;
| 6-(2-fluorophenyl)-2-methyl-9-nitro-2,&lt;br /&gt;
5-diazabicyclo[5.4.0]undeca-5,8,10,12-&lt;br /&gt;
tetraen-3-one&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Chemical_formula Molecular formula]&lt;br /&gt;
| C16H12FN3O3&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Molar_mass Molar mass]&lt;br /&gt;
| 313.3&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
| Appearance&lt;br /&gt;
| White, light yellow crystalline powder&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/CAS_registry_number CAS number]&lt;br /&gt;
| 1622-62-4&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Properties&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Solubility Solubility]&lt;br /&gt;
| Almost insoluble in water but soluble in alcohol&amp;lt;!--  at least put miscible with, not soluble in --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
&amp;lt;!-- | Other solvents e.g. [[ethanol]], [[acetone]] --&amp;gt;&lt;br /&gt;
&amp;lt;!-- | solubility info on other solvents --&amp;gt;&lt;br /&gt;
&amp;lt;!-- |- --&amp;gt;&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Melting_point Melting point]&lt;br /&gt;
| 168-172 C &amp;lt;!-- (mention any decomposition) --&amp;gt;&lt;br /&gt;
|}&lt;br /&gt;
===Rohypnol (Flunitrazepam) ===&lt;br /&gt;
&amp;lt;jmol&amp;gt;&lt;br /&gt;
&amp;lt;jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;size&amp;gt;200&amp;lt;/size&amp;gt;&lt;br /&gt;
&amp;lt;color&amp;gt;white&amp;lt;/color&amp;gt;&lt;br /&gt;
&amp;lt;script&amp;gt;zoom 80; cpk on;frame 1; move 10 -20 10 0 0 0 0 0 3; delay 1;&amp;lt;/script&amp;gt;&lt;br /&gt;
&amp;lt;inlineContents&amp;gt;Molecule-1&lt;br /&gt;
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   -0.1468   -3.1289    0.0744 C   0  0  0  0  0  0  0  0  0 13&lt;br /&gt;
    2.4132    0.3587   -0.0518 C   0  0  0  0  0  0  0  0  0 14&lt;br /&gt;
   -0.9304   -4.2097   -0.0863 C   0  0  0  0  0  0  0  0  0 15&lt;br /&gt;
    1.3200   -3.4239    0.2878 C   0  0  0  0  0  0  0  0  0 16&lt;br /&gt;
    3.7354   -0.0966   -0.0725 N   0  0  0  0  0  0  0  0  0 17&lt;br /&gt;
   -2.2471   -4.0952   -0.2850 F   0  0  0  0  0  0  0  0  0 18&lt;br /&gt;
   -0.3488   -5.5718   -0.0633 C   0  0  0  0  0  0  0  0  0 19&lt;br /&gt;
    1.8237   -4.6496    0.3045 C   0  0  0  0  0  0  0  0  0 20&lt;br /&gt;
    4.3160    0.9210   -0.0766 O   0  0  0  0  0  0  0  0  0 21&lt;br /&gt;
    3.5371   -1.2593   -0.0741 O   0  0  0  0  0  0  0  0  0 22&lt;br /&gt;
    0.9533   -5.7735    0.1176 C   0  0  0  0  0  0  0  0  0 23&lt;br /&gt;
  1  2  1  0  0  0&lt;br /&gt;
  2  3  1  0  0  0&lt;br /&gt;
  2  4  1  0  0  0&lt;br /&gt;
  3  5  1  0  0  0&lt;br /&gt;
  3  6  2  0  0  0&lt;br /&gt;
  4  7  2  0  0  0&lt;br /&gt;
  4  8  1  0  0  0&lt;br /&gt;
  5  9  1  0  0  0&lt;br /&gt;
  5 10  2  0  0  0&lt;br /&gt;
  6 11  1  0  0  0&lt;br /&gt;
  8 12  1  0  0  0&lt;br /&gt;
  9 12  2  0  0  0&lt;br /&gt;
  9 13  1  0  0  0&lt;br /&gt;
 10 14  1  0  0  0&lt;br /&gt;
 11 14  2  0  0  0&lt;br /&gt;
 13 15  2  0  0  0&lt;br /&gt;
 13 16  1  0  0  0&lt;br /&gt;
 14 17  1  0  0  0&lt;br /&gt;
 15 18  1  0  0  0&lt;br /&gt;
 15 19  1  0  0  0&lt;br /&gt;
 16 20  2  0  0  0&lt;br /&gt;
 17 21  2  0  0  0&lt;br /&gt;
 17 22  2  0  0  0&lt;br /&gt;
 19 23  2  0  0  0&lt;br /&gt;
 20 23  1  0  0  0&lt;br /&gt;
M  END&lt;br /&gt;
title1&lt;br /&gt;
title2&lt;br /&gt;
&lt;br /&gt;
M  END&amp;lt;/inlineContents&amp;gt;&lt;br /&gt;
&amp;lt;/jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;/jmol&amp;gt;&lt;/div&gt;</summary>
		<author><name>Wwl06</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=Rohypnol&amp;diff=12096</id>
		<title>Rohypnol</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=Rohypnol&amp;diff=12096"/>
		<updated>2007-11-27T16:23:37Z</updated>

		<summary type="html">&lt;p&gt;Wwl06: /* Rohypnol (Flunitrazepam) */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&amp;lt;noinclude&amp;gt;&lt;br /&gt;
&amp;lt;!-- This template has been defined after elaborate discussion in the Chemicals Wikiproject. Please do not add, deleted or otherwise change it unless after due discussion in [[wikipedia talk:WikiProject Chemicals]] --&amp;gt;&lt;br /&gt;
&amp;lt;/noinclude&amp;gt;{| class=&amp;quot;toccolours&amp;quot; border=&amp;quot;1&amp;quot; style=&amp;quot;float: right; clear: right; margin: 0 0 1em 1em; border-collapse: collapse; width: 280px&amp;quot;&lt;br /&gt;
! {{chembox header}} | {{PAGENAME}} &amp;lt;!-- replace if not identical with the article name --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image:{{PAGENAME}}.jpg|200px|{{PAGENAME}}]] &amp;lt;!-- replace if not identical with the pagename --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | General&lt;br /&gt;
|- &lt;br /&gt;
| [http://en.wikipedia.org/wiki/IUPAC Systematic name]&lt;br /&gt;
| 6-(2-fluorophenyl)-2-methyl-9-nitro-2,&lt;br /&gt;
5-diazabicyclo[5.4.0]undeca-5,8,10,12-&lt;br /&gt;
tetraen-3-one&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Chemical_formula Molecular formula]&lt;br /&gt;
| C16H12FN3O3&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Molar_mass Molar mass]&lt;br /&gt;
| 313.3&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
| Appearance&lt;br /&gt;
| White, light yellow crystalline powder&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/CAS_registry_number CAS number]&lt;br /&gt;
| 1622-62-4&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Properties&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Solubility Solubility]&lt;br /&gt;
| Almost insoluble in water but soluble in alcohol&amp;lt;!--  at least put miscible with, not soluble in --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
&amp;lt;!-- | Other solvents e.g. [[ethanol]], [[acetone]] --&amp;gt;&lt;br /&gt;
&amp;lt;!-- | solubility info on other solvents --&amp;gt;&lt;br /&gt;
&amp;lt;!-- |- --&amp;gt;&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Melting_point Melting point]&lt;br /&gt;
| 168-172 C &amp;lt;!-- (mention any decomposition) --&amp;gt;&lt;br /&gt;
|}&lt;br /&gt;
===Rohypnol (Flunitrazepam) ===&lt;br /&gt;
&amp;lt;jmol&amp;gt;&lt;br /&gt;
&amp;lt;jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;size&amp;gt;200&amp;lt;/size&amp;gt;&lt;br /&gt;
&amp;lt;color&amp;gt;white&amp;lt;/color&amp;gt;&lt;br /&gt;
&amp;lt;script&amp;gt;zoom 80; cpk on;frame 1; move 10 -20 10 0 0 0 0 0 3; delay 1;&amp;lt;/script&amp;gt;&lt;br /&gt;
&amp;lt;inlineContents&amp;gt;rohypnol.mol&lt;br /&gt;
title1&lt;br /&gt;
title2&lt;br /&gt;
&lt;br /&gt;
M  END&amp;lt;/inlineContents&amp;gt;&lt;br /&gt;
&amp;lt;/jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;/jmol&amp;gt;&lt;/div&gt;</summary>
		<author><name>Wwl06</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=Rohypnol&amp;diff=12093</id>
		<title>Rohypnol</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=Rohypnol&amp;diff=12093"/>
		<updated>2007-11-27T16:21:45Z</updated>

		<summary type="html">&lt;p&gt;Wwl06: /* Rohypnol (Flunitrazepam) */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&amp;lt;noinclude&amp;gt;&lt;br /&gt;
&amp;lt;!-- This template has been defined after elaborate discussion in the Chemicals Wikiproject. Please do not add, deleted or otherwise change it unless after due discussion in [[wikipedia talk:WikiProject Chemicals]] --&amp;gt;&lt;br /&gt;
&amp;lt;/noinclude&amp;gt;{| class=&amp;quot;toccolours&amp;quot; border=&amp;quot;1&amp;quot; style=&amp;quot;float: right; clear: right; margin: 0 0 1em 1em; border-collapse: collapse; width: 280px&amp;quot;&lt;br /&gt;
! {{chembox header}} | {{PAGENAME}} &amp;lt;!-- replace if not identical with the article name --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image:{{PAGENAME}}.jpg|200px|{{PAGENAME}}]] &amp;lt;!-- replace if not identical with the pagename --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | General&lt;br /&gt;
|- &lt;br /&gt;
| [http://en.wikipedia.org/wiki/IUPAC Systematic name]&lt;br /&gt;
| 6-(2-fluorophenyl)-2-methyl-9-nitro-2,&lt;br /&gt;
5-diazabicyclo[5.4.0]undeca-5,8,10,12-&lt;br /&gt;
tetraen-3-one&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Chemical_formula Molecular formula]&lt;br /&gt;
| C16H12FN3O3&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Molar_mass Molar mass]&lt;br /&gt;
| 313.3&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
| Appearance&lt;br /&gt;
| White, light yellow crystalline powder&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/CAS_registry_number CAS number]&lt;br /&gt;
| 1622-62-4&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Properties&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Solubility Solubility]&lt;br /&gt;
| Almost insoluble in water but soluble in alcohol&amp;lt;!--  at least put miscible with, not soluble in --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
&amp;lt;!-- | Other solvents e.g. [[ethanol]], [[acetone]] --&amp;gt;&lt;br /&gt;
&amp;lt;!-- | solubility info on other solvents --&amp;gt;&lt;br /&gt;
&amp;lt;!-- |- --&amp;gt;&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Melting_point Melting point]&lt;br /&gt;
| 168-172 C &amp;lt;!-- (mention any decomposition) --&amp;gt;&lt;br /&gt;
|}&lt;br /&gt;
===Rohypnol (Flunitrazepam) ===&lt;br /&gt;
&amp;lt;jmol&amp;gt;&lt;br /&gt;
&amp;lt;jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;size&amp;gt;200&amp;lt;/size&amp;gt;&lt;br /&gt;
&amp;lt;color&amp;gt;white&amp;lt;/color&amp;gt;&lt;br /&gt;
&amp;lt;script&amp;gt;zoom 80; cpk on;frame 1; move 10 -20 10 0 0 0 0 0 3; delay 1;&amp;lt;/script&amp;gt;&lt;br /&gt;
&amp;lt;inlineContents&amp;gt;rohypnol.mol&lt;br /&gt;
title1&lt;br /&gt;
title2&lt;br /&gt;
  3  2  0  0  0                 1 V2000&lt;br /&gt;
   -1.0400    1.5290    0.0000 O   0  0  0  0  0&lt;br /&gt;
   -1.0331    2.4710    0.0000 H   0  0  0  0  0&lt;br /&gt;
   -1.9535    1.2993    0.0000 H   0  0  0  0  0&lt;br /&gt;
  1  2  1  0  0  0&lt;br /&gt;
  1  3  1  0  0  0&lt;br /&gt;
M  END&amp;lt;/inlineContents&amp;gt;&lt;br /&gt;
&amp;lt;/jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;/jmol&amp;gt;&lt;/div&gt;</summary>
		<author><name>Wwl06</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=Rohypnol&amp;diff=12090</id>
		<title>Rohypnol</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=Rohypnol&amp;diff=12090"/>
		<updated>2007-11-27T16:15:33Z</updated>

		<summary type="html">&lt;p&gt;Wwl06: /* Rohypnol (Flunitrazepam) */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&amp;lt;noinclude&amp;gt;&lt;br /&gt;
&amp;lt;!-- This template has been defined after elaborate discussion in the Chemicals Wikiproject. Please do not add, deleted or otherwise change it unless after due discussion in [[wikipedia talk:WikiProject Chemicals]] --&amp;gt;&lt;br /&gt;
&amp;lt;/noinclude&amp;gt;{| class=&amp;quot;toccolours&amp;quot; border=&amp;quot;1&amp;quot; style=&amp;quot;float: right; clear: right; margin: 0 0 1em 1em; border-collapse: collapse; width: 280px&amp;quot;&lt;br /&gt;
! {{chembox header}} | {{PAGENAME}} &amp;lt;!-- replace if not identical with the article name --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image:{{PAGENAME}}.jpg|200px|{{PAGENAME}}]] &amp;lt;!-- replace if not identical with the pagename --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | General&lt;br /&gt;
|- &lt;br /&gt;
| [http://en.wikipedia.org/wiki/IUPAC Systematic name]&lt;br /&gt;
| 6-(2-fluorophenyl)-2-methyl-9-nitro-2,&lt;br /&gt;
5-diazabicyclo[5.4.0]undeca-5,8,10,12-&lt;br /&gt;
tetraen-3-one&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Chemical_formula Molecular formula]&lt;br /&gt;
| C16H12FN3O3&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Molar_mass Molar mass]&lt;br /&gt;
| 313.3&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
| Appearance&lt;br /&gt;
| White, light yellow crystalline powder&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/CAS_registry_number CAS number]&lt;br /&gt;
| 1622-62-4&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Properties&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Solubility Solubility]&lt;br /&gt;
| Almost insoluble in water but soluble in alcohol&amp;lt;!--  at least put miscible with, not soluble in --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
&amp;lt;!-- | Other solvents e.g. [[ethanol]], [[acetone]] --&amp;gt;&lt;br /&gt;
&amp;lt;!-- | solubility info on other solvents --&amp;gt;&lt;br /&gt;
&amp;lt;!-- |- --&amp;gt;&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Melting_point Melting point]&lt;br /&gt;
| 168-172 C &amp;lt;!-- (mention any decomposition) --&amp;gt;&lt;br /&gt;
|}&lt;br /&gt;
===Rohypnol (Flunitrazepam) ===&lt;br /&gt;
&amp;lt;jmol&amp;gt;&lt;br /&gt;
&amp;lt;jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;size&amp;gt;200&amp;lt;/size&amp;gt;&lt;br /&gt;
&amp;lt;color&amp;gt;white&amp;lt;/color&amp;gt;&lt;br /&gt;
&amp;lt;script&amp;gt;zoom 80; cpk on;frame 1; move 10 -20 10 0 0 0 0 0 3; delay 1;&amp;lt;/script&amp;gt;&lt;br /&gt;
&amp;lt;inlineContents&amp;gt;water.mol&lt;br /&gt;
title1&lt;br /&gt;
title2&lt;br /&gt;
  3  2  0  0  0                 1 V2000&lt;br /&gt;
   -1.0400    1.5290    0.0000 O   0  0  0  0  0&lt;br /&gt;
   -1.0331    2.4710    0.0000 H   0  0  0  0  0&lt;br /&gt;
   -1.9535    1.2993    0.0000 H   0  0  0  0  0&lt;br /&gt;
  1  2  1  0  0  0&lt;br /&gt;
  1  3  1  0  0  0&lt;br /&gt;
M  END&amp;lt;/inlineContents&amp;gt;&lt;br /&gt;
&amp;lt;/jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;/jmol&amp;gt;&lt;/div&gt;</summary>
		<author><name>Wwl06</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=Rohypnol&amp;diff=12089</id>
		<title>Rohypnol</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=Rohypnol&amp;diff=12089"/>
		<updated>2007-11-27T16:01:57Z</updated>

		<summary type="html">&lt;p&gt;Wwl06: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&amp;lt;noinclude&amp;gt;&lt;br /&gt;
&amp;lt;!-- This template has been defined after elaborate discussion in the Chemicals Wikiproject. Please do not add, deleted or otherwise change it unless after due discussion in [[wikipedia talk:WikiProject Chemicals]] --&amp;gt;&lt;br /&gt;
&amp;lt;/noinclude&amp;gt;{| class=&amp;quot;toccolours&amp;quot; border=&amp;quot;1&amp;quot; style=&amp;quot;float: right; clear: right; margin: 0 0 1em 1em; border-collapse: collapse; width: 280px&amp;quot;&lt;br /&gt;
! {{chembox header}} | {{PAGENAME}} &amp;lt;!-- replace if not identical with the article name --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image:{{PAGENAME}}.jpg|200px|{{PAGENAME}}]] &amp;lt;!-- replace if not identical with the pagename --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | General&lt;br /&gt;
|- &lt;br /&gt;
| [http://en.wikipedia.org/wiki/IUPAC Systematic name]&lt;br /&gt;
| 6-(2-fluorophenyl)-2-methyl-9-nitro-2,&lt;br /&gt;
5-diazabicyclo[5.4.0]undeca-5,8,10,12-&lt;br /&gt;
tetraen-3-one&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Chemical_formula Molecular formula]&lt;br /&gt;
| C16H12FN3O3&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Molar_mass Molar mass]&lt;br /&gt;
| 313.3&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
| Appearance&lt;br /&gt;
| White, light yellow crystalline powder&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/CAS_registry_number CAS number]&lt;br /&gt;
| 1622-62-4&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Properties&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Solubility Solubility]&lt;br /&gt;
| Almost insoluble in water but soluble in alcohol&amp;lt;!--  at least put miscible with, not soluble in --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
&amp;lt;!-- | Other solvents e.g. [[ethanol]], [[acetone]] --&amp;gt;&lt;br /&gt;
&amp;lt;!-- | solubility info on other solvents --&amp;gt;&lt;br /&gt;
&amp;lt;!-- |- --&amp;gt;&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Melting_point Melting point]&lt;br /&gt;
| 168-172 C &amp;lt;!-- (mention any decomposition) --&amp;gt;&lt;br /&gt;
|}&lt;br /&gt;
===Rohypnol (Flunitrazepam) ===&lt;/div&gt;</summary>
		<author><name>Wwl06</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=Rohypnol&amp;diff=12088</id>
		<title>Rohypnol</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=Rohypnol&amp;diff=12088"/>
		<updated>2007-11-27T16:00:44Z</updated>

		<summary type="html">&lt;p&gt;Wwl06: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;br /&gt;
&amp;lt;noinclude&amp;gt;&lt;br /&gt;
&amp;lt;!-- This template has been defined after elaborate discussion in the Chemicals Wikiproject. Please do not add, deleted or otherwise change it unless after due discussion in [[wikipedia talk:WikiProject Chemicals]] --&amp;gt;&lt;br /&gt;
&amp;lt;/noinclude&amp;gt;{| class=&amp;quot;toccolours&amp;quot; border=&amp;quot;1&amp;quot; style=&amp;quot;float: right; clear: right; margin: 0 0 1em 1em; border-collapse: collapse; width: 280px&amp;quot;&lt;br /&gt;
! {{chembox header}} | {{PAGENAME}} &amp;lt;!-- replace if not identical with the article name --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image:{{PAGENAME}}.jpg|200px|{{PAGENAME}}]] &amp;lt;!-- replace if not identical with the pagename --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | General&lt;br /&gt;
|- &lt;br /&gt;
| [http://en.wikipedia.org/wiki/IUPAC Systematic name]&lt;br /&gt;
| 6-(2-fluorophenyl)-2-methyl-9-nitro-2,&lt;br /&gt;
5-diazabicyclo[5.4.0]undeca-5,8,10,12-&lt;br /&gt;
tetraen-3-one&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Chemical_formula Molecular formula]&lt;br /&gt;
| C16H12FN3O3&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Molar_mass Molar mass]&lt;br /&gt;
| 313.3&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
| Appearance&lt;br /&gt;
| White, light yellow crystalline powder&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/CAS_registry_number CAS number]&lt;br /&gt;
| 1622-62-4&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Properties&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Solubility Solubility]&lt;br /&gt;
| Almost insoluble in water but soluble in alcohol&amp;lt;!--  at least put miscible with, not soluble in --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
&amp;lt;!-- | Other solvents e.g. [[ethanol]], [[acetone]] --&amp;gt;&lt;br /&gt;
&amp;lt;!-- | solubility info on other solvents --&amp;gt;&lt;br /&gt;
&amp;lt;!-- |- --&amp;gt;&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Melting_point Melting point]&lt;br /&gt;
| 168-172 C &amp;lt;!-- (mention any decomposition) --&amp;gt;&lt;br /&gt;
&lt;br /&gt;
===Rohypnol (Flunitrazepam) ===&lt;/div&gt;</summary>
		<author><name>Wwl06</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=Rohypnol&amp;diff=12084</id>
		<title>Rohypnol</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=Rohypnol&amp;diff=12084"/>
		<updated>2007-11-27T15:42:16Z</updated>

		<summary type="html">&lt;p&gt;Wwl06: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;br /&gt;
&lt;br /&gt;
&amp;lt;noinclude&amp;gt;&lt;br /&gt;
&amp;lt;!-- This template has been defined after elaborate discussion in the Chemicals Wikiproject. Please do not add, deleted or otherwise change it unless after due discussion in [[wikipedia talk:WikiProject Chemicals]] --&amp;gt;&lt;br /&gt;
&amp;lt;/noinclude&amp;gt;{| class=&amp;quot;toccolours&amp;quot; border=&amp;quot;1&amp;quot; style=&amp;quot;float: right; clear: right; margin: 0 0 1em 1em; border-collapse: collapse; width: 280px&amp;quot;&lt;br /&gt;
! {{chembox header}} | {{PAGENAME}} &amp;lt;!-- replace if not identical with the article name --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image:{{PAGENAME}}.jpg|200px|{{PAGENAME}}]] &amp;lt;!-- replace if not identical with the pagename --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | General&lt;br /&gt;
|- &lt;br /&gt;
| [http://en.wikipedia.org/wiki/IUPAC Systematic name]&lt;br /&gt;
| 6-(2-fluorophenyl)-2-methyl-9-nitro-2,&lt;br /&gt;
5-diazabicyclo[5.4.0]undeca-5,8,10,12-&lt;br /&gt;
tetraen-3-one&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Chemical_formula Molecular formula]&lt;br /&gt;
| C16H12FN3O3&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Molar_mass Molar mass]&lt;br /&gt;
| 313.3&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
| Appearance&lt;br /&gt;
| White, light yellow crystalline powder&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/CAS_registry_number CAS number]&lt;br /&gt;
| 1622-62-4&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Properties&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Solubility Solubility]&lt;br /&gt;
| Almost insoluble in water but soluble in alcohol&amp;lt;!--  at least put miscible with, not soluble in --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
&amp;lt;!-- | Other solvents e.g. [[ethanol]], [[acetone]] --&amp;gt;&lt;br /&gt;
&amp;lt;!-- | solubility info on other solvents --&amp;gt;&lt;br /&gt;
&amp;lt;!-- |- --&amp;gt;&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Melting_point Melting point]&lt;br /&gt;
| 168-172 C &amp;lt;!-- (mention any decomposition) --&amp;gt;&lt;/div&gt;</summary>
		<author><name>Wwl06</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=Rohypnol&amp;diff=12083</id>
		<title>Rohypnol</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=Rohypnol&amp;diff=12083"/>
		<updated>2007-11-27T15:42:04Z</updated>

		<summary type="html">&lt;p&gt;Wwl06: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;khkjnmk&lt;br /&gt;
vghf&lt;br /&gt;
&lt;br /&gt;
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&lt;br /&gt;
fdgdfg&lt;br /&gt;
&lt;br /&gt;
&amp;lt;noinclude&amp;gt;&lt;br /&gt;
&amp;lt;!-- This template has been defined after elaborate discussion in the Chemicals Wikiproject. Please do not add, deleted or otherwise change it unless after due discussion in [[wikipedia talk:WikiProject Chemicals]] --&amp;gt;&lt;br /&gt;
&amp;lt;/noinclude&amp;gt;{| class=&amp;quot;toccolours&amp;quot; border=&amp;quot;1&amp;quot; style=&amp;quot;float: right; clear: right; margin: 0 0 1em 1em; border-collapse: collapse; width: 280px&amp;quot;&lt;br /&gt;
! {{chembox header}} | {{PAGENAME}} &amp;lt;!-- replace if not identical with the article name --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image:{{PAGENAME}}.jpg|200px|{{PAGENAME}}]] &amp;lt;!-- replace if not identical with the pagename --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | General&lt;br /&gt;
|- &lt;br /&gt;
| [http://en.wikipedia.org/wiki/IUPAC Systematic name]&lt;br /&gt;
| 6-(2-fluorophenyl)-2-methyl-9-nitro-2,&lt;br /&gt;
5-diazabicyclo[5.4.0]undeca-5,8,10,12-&lt;br /&gt;
tetraen-3-one&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Chemical_formula Molecular formula]&lt;br /&gt;
| C16H12FN3O3&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Molar_mass Molar mass]&lt;br /&gt;
| 313.3&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
| Appearance&lt;br /&gt;
| White, light yellow crystalline powder&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/CAS_registry_number CAS number]&lt;br /&gt;
| 1622-62-4&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Properties&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Solubility Solubility]&lt;br /&gt;
| Almost insoluble in water but soluble in alcohol&amp;lt;!--  at least put miscible with, not soluble in --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
&amp;lt;!-- | Other solvents e.g. [[ethanol]], [[acetone]] --&amp;gt;&lt;br /&gt;
&amp;lt;!-- | solubility info on other solvents --&amp;gt;&lt;br /&gt;
&amp;lt;!-- |- --&amp;gt;&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Melting_point Melting point]&lt;br /&gt;
| 168-172 C &amp;lt;!-- (mention any decomposition) --&amp;gt;&lt;/div&gt;</summary>
		<author><name>Wwl06</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=Rohypnol&amp;diff=12082</id>
		<title>Rohypnol</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=Rohypnol&amp;diff=12082"/>
		<updated>2007-11-27T15:41:44Z</updated>

		<summary type="html">&lt;p&gt;Wwl06: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;br /&gt;
khkjnmk&lt;br /&gt;
&lt;br /&gt;
&amp;lt;noinclude&amp;gt;&lt;br /&gt;
&amp;lt;!-- This template has been defined after elaborate discussion in the Chemicals Wikiproject. Please do not add, deleted or otherwise change it unless after due discussion in [[wikipedia talk:WikiProject Chemicals]] --&amp;gt;&lt;br /&gt;
&amp;lt;/noinclude&amp;gt;{| class=&amp;quot;toccolours&amp;quot; border=&amp;quot;1&amp;quot; style=&amp;quot;float: right; clear: right; margin: 0 0 1em 1em; border-collapse: collapse; width: 280px&amp;quot;&lt;br /&gt;
! {{chembox header}} | {{PAGENAME}} &amp;lt;!-- replace if not identical with the article name --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image:{{PAGENAME}}.jpg|200px|{{PAGENAME}}]] &amp;lt;!-- replace if not identical with the pagename --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | General&lt;br /&gt;
|- &lt;br /&gt;
| [http://en.wikipedia.org/wiki/IUPAC Systematic name]&lt;br /&gt;
| 6-(2-fluorophenyl)-2-methyl-9-nitro-2,&lt;br /&gt;
5-diazabicyclo[5.4.0]undeca-5,8,10,12-&lt;br /&gt;
tetraen-3-one&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Chemical_formula Molecular formula]&lt;br /&gt;
| C16H12FN3O3&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Molar_mass Molar mass]&lt;br /&gt;
| 313.3&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
| Appearance&lt;br /&gt;
| White, light yellow crystalline powder&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/CAS_registry_number CAS number]&lt;br /&gt;
| 1622-62-4&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Properties&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Solubility Solubility]&lt;br /&gt;
| Almost insoluble in water but soluble in alcohol&amp;lt;!--  at least put miscible with, not soluble in --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
&amp;lt;!-- | Other solvents e.g. [[ethanol]], [[acetone]] --&amp;gt;&lt;br /&gt;
&amp;lt;!-- | solubility info on other solvents --&amp;gt;&lt;br /&gt;
&amp;lt;!-- |- --&amp;gt;&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Melting_point Melting point]&lt;br /&gt;
| 168-172 C &amp;lt;!-- (mention any decomposition) --&amp;gt;&lt;/div&gt;</summary>
		<author><name>Wwl06</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=Rohypnol&amp;diff=12081</id>
		<title>Rohypnol</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=Rohypnol&amp;diff=12081"/>
		<updated>2007-11-27T15:41:26Z</updated>

		<summary type="html">&lt;p&gt;Wwl06: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&amp;lt;noinclude&amp;gt;&lt;br /&gt;
&amp;lt;!-- This template has been defined after elaborate discussion in the Chemicals Wikiproject. Please do not add, deleted or otherwise change it unless after due discussion in [[wikipedia talk:WikiProject Chemicals]] --&amp;gt;&lt;br /&gt;
&amp;lt;/noinclude&amp;gt;{| class=&amp;quot;toccolours&amp;quot; border=&amp;quot;1&amp;quot; style=&amp;quot;float: right; clear: right; margin: 0 0 1em 1em; border-collapse: collapse; width: 280px&amp;quot;&lt;br /&gt;
! {{chembox header}} | {{PAGENAME}} &amp;lt;!-- replace if not identical with the article name --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image:{{PAGENAME}}.jpg|200px|{{PAGENAME}}]] &amp;lt;!-- replace if not identical with the pagename --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | General&lt;br /&gt;
|- &lt;br /&gt;
| [http://en.wikipedia.org/wiki/IUPAC Systematic name]&lt;br /&gt;
| 6-(2-fluorophenyl)-2-methyl-9-nitro-2,&lt;br /&gt;
5-diazabicyclo[5.4.0]undeca-5,8,10,12-&lt;br /&gt;
tetraen-3-one&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Chemical_formula Molecular formula]&lt;br /&gt;
| C16H12FN3O3&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Molar_mass Molar mass]&lt;br /&gt;
| 313.3&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
| Appearance&lt;br /&gt;
| White, light yellow crystalline powder&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/CAS_registry_number CAS number]&lt;br /&gt;
| 1622-62-4&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Properties&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Solubility Solubility]&lt;br /&gt;
| Almost insoluble in water but soluble in alcohol&amp;lt;!--  at least put miscible with, not soluble in --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
&amp;lt;!-- | Other solvents e.g. [[ethanol]], [[acetone]] --&amp;gt;&lt;br /&gt;
&amp;lt;!-- | solubility info on other solvents --&amp;gt;&lt;br /&gt;
&amp;lt;!-- |- --&amp;gt;&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Melting_point Melting point]&lt;br /&gt;
| 168-172 C &amp;lt;!-- (mention any decomposition) --&amp;gt;&lt;/div&gt;</summary>
		<author><name>Wwl06</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=Rohypnol&amp;diff=12080</id>
		<title>Rohypnol</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=Rohypnol&amp;diff=12080"/>
		<updated>2007-11-27T15:41:17Z</updated>

		<summary type="html">&lt;p&gt;Wwl06: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&amp;lt;noinclude&amp;gt;&lt;br /&gt;
&amp;lt;!-- This template has been defined after elaborate discussion in the Chemicals Wikiproject. Please do not add, deleted or otherwise change it unless after due discussion in [[wikipedia talk:WikiProject Chemicals]] --&amp;gt;&lt;br /&gt;
&amp;lt;/noinclude&amp;gt;{| class=&amp;quot;toccolours&amp;quot; border=&amp;quot;1&amp;quot; style=&amp;quot;float: right; clear: right; margin: 0 0 1em 1em; border-collapse: collapse; width: 280px&amp;quot;&lt;br /&gt;
! {{chembox header}} | {{PAGENAME}} &amp;lt;!-- replace if not identical with the article name --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image:{{PAGENAME}}.jpg|200px|{{PAGENAME}}]] &amp;lt;!-- replace if not identical with the pagename --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | General&lt;br /&gt;
|- &lt;br /&gt;
| [http://en.wikipedia.org/wiki/IUPAC Systematic name]&lt;br /&gt;
| 6-(2-fluorophenyl)-2-methyl-9-nitro-2,&lt;br /&gt;
5-diazabicyclo[5.4.0]undeca-5,8,10,12-&lt;br /&gt;
tetraen-3-one&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Chemical_formula Molecular formula]&lt;br /&gt;
| C16H12FN3O3&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Molar_mass Molar mass]&lt;br /&gt;
| 313.3&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
| Appearance&lt;br /&gt;
| White, light yellow crystalline powder&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/CAS_registry_number CAS number]&lt;br /&gt;
| 1622-62-4&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Properties&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Solubility Solubility]&lt;br /&gt;
| Almost insoluble in water but soluble in alcohol&amp;lt;!--  at least put miscible with, not soluble in --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
&amp;lt;!-- | Other solvents e.g. [[ethanol]], [[acetone]] --&amp;gt;&lt;br /&gt;
&amp;lt;!-- | solubility info on other solvents --&amp;gt;&lt;br /&gt;
&amp;lt;!-- |- --&amp;gt;&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Melting_point Melting point]&lt;br /&gt;
| 168-172 C &amp;lt;!-- (mention any decomposition) --&amp;gt;&lt;br /&gt;
&lt;br /&gt;
kmkln&lt;/div&gt;</summary>
		<author><name>Wwl06</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=Rohypnol&amp;diff=12079</id>
		<title>Rohypnol</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=Rohypnol&amp;diff=12079"/>
		<updated>2007-11-27T15:41:02Z</updated>

		<summary type="html">&lt;p&gt;Wwl06: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&amp;lt;noinclude&amp;gt;&lt;br /&gt;
&amp;lt;!-- This template has been defined after elaborate discussion in the Chemicals Wikiproject. Please do not add, deleted or otherwise change it unless after due discussion in [[wikipedia talk:WikiProject Chemicals]] --&amp;gt;&lt;br /&gt;
&amp;lt;/noinclude&amp;gt;{| class=&amp;quot;toccolours&amp;quot; border=&amp;quot;1&amp;quot; style=&amp;quot;float: right; clear: right; margin: 0 0 1em 1em; border-collapse: collapse; width: 280px&amp;quot;&lt;br /&gt;
! {{chembox header}} | {{PAGENAME}} &amp;lt;!-- replace if not identical with the article name --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image:{{PAGENAME}}.jpg|200px|{{PAGENAME}}]] &amp;lt;!-- replace if not identical with the pagename --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | General&lt;br /&gt;
|- &lt;br /&gt;
| [http://en.wikipedia.org/wiki/IUPAC Systematic name]&lt;br /&gt;
| 6-(2-fluorophenyl)-2-methyl-9-nitro-2,&lt;br /&gt;
5-diazabicyclo[5.4.0]undeca-5,8,10,12-&lt;br /&gt;
tetraen-3-one&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Chemical_formula Molecular formula]&lt;br /&gt;
| C16H12FN3O3&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Molar_mass Molar mass]&lt;br /&gt;
| 313.3&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
| Appearance&lt;br /&gt;
| White, light yellow crystalline powder&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/CAS_registry_number CAS number]&lt;br /&gt;
| 1622-62-4&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Properties&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Solubility Solubility]&lt;br /&gt;
| Almost insoluble in water but soluble in alcohol&amp;lt;!--  at least put miscible with, not soluble in --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
&amp;lt;!-- | Other solvents e.g. [[ethanol]], [[acetone]] --&amp;gt;&lt;br /&gt;
&amp;lt;!-- | solubility info on other solvents --&amp;gt;&lt;br /&gt;
&amp;lt;!-- |- --&amp;gt;&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Melting_point Melting point]&lt;br /&gt;
| 168-172 C &amp;lt;!-- (mention any decomposition) --&amp;gt;&lt;/div&gt;</summary>
		<author><name>Wwl06</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=Rohypnol&amp;diff=12078</id>
		<title>Rohypnol</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=Rohypnol&amp;diff=12078"/>
		<updated>2007-11-27T15:40:38Z</updated>

		<summary type="html">&lt;p&gt;Wwl06: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&amp;lt;noinclude&amp;gt;&lt;br /&gt;
&amp;lt;!-- This template has been defined after elaborate discussion in the Chemicals Wikiproject. Please do not add, deleted or otherwise change it unless after due discussion in [[wikipedia talk:WikiProject Chemicals]] --&amp;gt;&lt;br /&gt;
&amp;lt;/noinclude&amp;gt;{| class=&amp;quot;toccolours&amp;quot; border=&amp;quot;1&amp;quot; style=&amp;quot;float: right; clear: right; margin: 0 0 1em 1em; border-collapse: collapse; width: 280px&amp;quot;&lt;br /&gt;
! {{chembox header}} | {{PAGENAME}} &amp;lt;!-- replace if not identical with the article name --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image:{{PAGENAME}}.jpg|200px|{{PAGENAME}}]] &amp;lt;!-- replace if not identical with the pagename --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | General&lt;br /&gt;
|- &lt;br /&gt;
| [http://en.wikipedia.org/wiki/IUPAC Systematic name]&lt;br /&gt;
| 6-(2-fluorophenyl)-2-methyl-9-nitro-2,&lt;br /&gt;
5-diazabicyclo[5.4.0]undeca-5,8,10,12-&lt;br /&gt;
tetraen-3-one&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
| Other names&lt;br /&gt;
| {{{OtherNames}}}&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Chemical_formula Molecular formula]&lt;br /&gt;
| C16H12FN3O3&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Molar_mass Molar mass]&lt;br /&gt;
| 313.3&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
| Appearance&lt;br /&gt;
| White, light yellow crystalline powder&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/CAS_registry_number CAS number]&lt;br /&gt;
| 1622-62-4&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Properties&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Density Density] &amp;amp; [http://en.wikipedia.org/wiki/Phase_%28matter%29 phase]&lt;br /&gt;
| {{{Density}}} g/cm³ &amp;lt;!-- ? g/cm³, solid / ? g/ml, liquid / ? g/l, gas --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Solubility Solubility]&lt;br /&gt;
| Almost insoluble in water but soluble in alcohol&amp;lt;!--  at least put miscible with, not soluble in --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
&amp;lt;!-- | Other solvents e.g. [[ethanol]], [[acetone]] --&amp;gt;&lt;br /&gt;
&amp;lt;!-- | solubility info on other solvents --&amp;gt;&lt;br /&gt;
&amp;lt;!-- |- --&amp;gt;&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Melting_point Melting point]&lt;br /&gt;
| 168-172 C &amp;lt;!-- (mention any decomposition) --&amp;gt;&lt;/div&gt;</summary>
		<author><name>Wwl06</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=Rohypnol&amp;diff=12077</id>
		<title>Rohypnol</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=Rohypnol&amp;diff=12077"/>
		<updated>2007-11-27T15:39:54Z</updated>

		<summary type="html">&lt;p&gt;Wwl06: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&amp;lt;noinclude&amp;gt;&lt;br /&gt;
&amp;lt;!-- This template has been defined after elaborate discussion in the Chemicals Wikiproject. Please do not add, deleted or otherwise change it unless after due discussion in [[wikipedia talk:WikiProject Chemicals]] --&amp;gt;&lt;br /&gt;
&amp;lt;/noinclude&amp;gt;{| class=&amp;quot;toccolours&amp;quot; border=&amp;quot;1&amp;quot; style=&amp;quot;float: right; clear: right; margin: 0 0 1em 1em; border-collapse: collapse; width: 280px&amp;quot;&lt;br /&gt;
! {{chembox header}} | {{PAGENAME}} &amp;lt;!-- replace if not identical with the article name --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image:{{PAGENAME}}.jpg|200px|{{PAGENAME}}]] &amp;lt;!-- replace if not identical with the pagename --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | General&lt;br /&gt;
|- &lt;br /&gt;
| [http://en.wikipedia.org/wiki/IUPAC Systematic name]&lt;br /&gt;
| 6-(2-fluorophenyl)-2-methyl-9-nitro-2,&lt;br /&gt;
5-diazabicyclo[5.4.0]undeca-5,8,10,12-&lt;br /&gt;
tetraen-3-one&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
| Other names&lt;br /&gt;
| {{{OtherNames}}}&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Chemical_formula Molecular formula]&lt;br /&gt;
| C16H12FN3O3&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Molar_mass Molar mass]&lt;br /&gt;
| 313.3&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
| Appearance&lt;br /&gt;
| White, light yellow crystalline powder&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/CAS_registry_number CAS number]&lt;br /&gt;
| 1622-62-4&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Properties&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Density Density] &amp;amp; [http://en.wikipedia.org/wiki/Phase_%28matter%29 phase]&lt;br /&gt;
| {{{Density}}} g/cm³ &amp;lt;!-- ? g/cm³, solid / ? g/ml, liquid / ? g/l, gas --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Solubility Solubility]&lt;br /&gt;
| Almost insoluble in water but soluble in alcohol&amp;lt;!--  at least put miscible with, not soluble in --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
&amp;lt;!-- | Other solvents e.g. [[ethanol]], [[acetone]] --&amp;gt;&lt;br /&gt;
&amp;lt;!-- | solubility info on other solvents --&amp;gt;&lt;br /&gt;
&amp;lt;!-- |- --&amp;gt;&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Melting_point Melting point]&lt;br /&gt;
| 168-172 C &amp;lt;!-- (mention any decomposition) --&amp;gt;&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Structure&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Orbital_hybridisation Molecular shape] &amp;lt;!-- for simple covalent molecules (omit for most large molecules, ionics and complexes) --&amp;gt;&lt;br /&gt;
| {{{Mol_Shape}}} &amp;lt;!-- e.g. trigonal bipyramidal --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Coordination_geometry Coordination&amp;lt;br /&amp;gt;geometry] &amp;lt;!-- for a metal complex or an ionic crystal, otherwise omit --&amp;gt;&lt;br /&gt;
| {{{Coordination}}} &amp;lt;!-- e.g. trigonal bipyramidal --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Crystal_structure Crystal structure] &amp;lt;!-- omit if not a solid --&amp;gt;&lt;br /&gt;
| {{{Crystal_Structure}}} &amp;lt;!-- e.g. [[triclinic]], [[monoclinic]], [[orthorhombic]], [[hexagonal]], [[rhombohedral|trigonal]], [[tetragonal]], [[cubic]], and mention &amp;quot;close packed&amp;quot; or similar.  You may also cite what class it belongs to, e.g. [[Cadmium_chloride#Crystal_structure|CdCl&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt;]]  --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [[Dipole#Molecular_dipoles|Dipole moment]]&lt;br /&gt;
| {{{DM}}} [[Debye|D]]&lt;/div&gt;</summary>
		<author><name>Wwl06</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=Rohypnol&amp;diff=12076</id>
		<title>Rohypnol</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=Rohypnol&amp;diff=12076"/>
		<updated>2007-11-27T15:39:18Z</updated>

		<summary type="html">&lt;p&gt;Wwl06: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&amp;lt;noinclude&amp;gt;&lt;br /&gt;
&amp;lt;!-- This template has been defined after elaborate discussion in the Chemicals Wikiproject. Please do not add, deleted or otherwise change it unless after due discussion in [[wikipedia talk:WikiProject Chemicals]] --&amp;gt;&lt;br /&gt;
&amp;lt;/noinclude&amp;gt;{| class=&amp;quot;toccolours&amp;quot; border=&amp;quot;1&amp;quot; style=&amp;quot;float: right; clear: right; margin: 0 0 1em 1em; border-collapse: collapse; width: 280px&amp;quot;&lt;br /&gt;
! {{chembox header}} | {{PAGENAME}} &amp;lt;!-- replace if not identical with the article name --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image:{{PAGENAME}}.jpg|200px|{{PAGENAME}}]] &amp;lt;!-- replace if not identical with the pagename --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | General&lt;br /&gt;
|- &lt;br /&gt;
| [http://en.wikipedia.org/wiki/IUPAC Systematic name]&lt;br /&gt;
| 6-(2-fluorophenyl)-2-methyl-9-nitro-2,&lt;br /&gt;
5-diazabicyclo[5.4.0]undeca-5,8,10,12-&lt;br /&gt;
tetraen-3-one&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
| Other names&lt;br /&gt;
| {{{OtherNames}}}&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Chemical_formula Molecular formula]&lt;br /&gt;
| C16H12FN3O3&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Molar_mass Molar mass]&lt;br /&gt;
| 313.3&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
| Appearance&lt;br /&gt;
| White, light yellow crystalline powder&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/CAS_registry_number CAS number]&lt;br /&gt;
| 1622-62-4&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Properties&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Density Density] &amp;amp; [http://en.wikipedia.org/wiki/Phase_%28matter%29 phase]&lt;br /&gt;
| {{{Density}}} g/cm³ &amp;lt;!-- ? g/cm³, solid / ? g/ml, liquid / ? g/l, gas --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Solubility Solubility]&lt;br /&gt;
| Almost insoluble in water but soluble in alcohol&amp;lt;!--  at least put miscible with, not soluble in --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
&amp;lt;!-- | Other solvents e.g. [[ethanol]], [[acetone]] --&amp;gt;&lt;br /&gt;
&amp;lt;!-- | solubility info on other solvents --&amp;gt;&lt;br /&gt;
&amp;lt;!-- |- --&amp;gt;&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Melting_point Melting point]&lt;br /&gt;
| 168-172 C &amp;lt;!-- (mention any decomposition) --&amp;gt;&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Structure&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Orbital_hybridisation Molecular shape] &amp;lt;!-- for simple covalent molecules (omit for most large molecules, ionics and complexes) --&amp;gt;&lt;br /&gt;
| {{{Mol_Shape}}} &amp;lt;!-- e.g. trigonal bipyramidal --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Coordination_geometry Coordination&amp;lt;br /&amp;gt;geometry] &amp;lt;!-- for a metal complex or an ionic crystal, otherwise omit --&amp;gt;&lt;br /&gt;
| {{{Coordination}}} &amp;lt;!-- e.g. trigonal bipyramidal --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Crystal_structure Crystal structure] &amp;lt;!-- omit if not a solid --&amp;gt;&lt;br /&gt;
| {{{Crystal_Structure}}} &amp;lt;!-- e.g. [[triclinic]], [[monoclinic]], [[orthorhombic]], [[hexagonal]], [[rhombohedral|trigonal]], [[tetragonal]], [[cubic]], and mention &amp;quot;close packed&amp;quot; or similar.  You may also cite what class it belongs to, e.g. [[Cadmium_chloride#Crystal_structure|CdCl&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt;]]  --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [[Dipole#Molecular_dipoles|Dipole moment]]&lt;br /&gt;
| {{{DM}}} [[Debye|D]]&lt;br /&gt;
&lt;br /&gt;
! {{chembox header}} | [[{{PAGENAME}} (data page)|Supplementary data page]]&lt;br /&gt;
|-&lt;br /&gt;
| [[{{PAGENAME}} (data page)#Structure and properties|Structure and&amp;lt;br /&amp;gt;properties]] &lt;br /&gt;
| [http://en.wikipedia.org/wiki/Refractive_index &#039;&#039;n&#039;&#039;], [http://en.wikipedia.org/wiki/Dielectric_constant ε&amp;lt;sub&amp;gt;r&amp;lt;/sub&amp;gt;], etc. &lt;br /&gt;
|-&lt;br /&gt;
| [[{{PAGENAME}} (data page)#Thermodynamic properties|Thermodynamic&amp;lt;br /&amp;gt;data]] &lt;br /&gt;
| Phase behaviour&amp;lt;br /&amp;gt;Solid, liquid, gas &lt;br /&gt;
|-&lt;br /&gt;
| [[{{PAGENAME}} (data page)#Spectral data|Spectral data]]&lt;br /&gt;
| [[UV/VIS spectroscopy|UV]], [[Infrared spectroscopy|IR]], [[nuclear magnetic resonance spectroscopy|NMR]], [[Mass spectrometry|MS]]&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Related compounds&lt;br /&gt;
|-&lt;br /&gt;
| Other [[Ion|anion]]s &amp;lt;!-- please omit if not applicable --&amp;gt;&lt;br /&gt;
| {{{Other_anion}}} &amp;lt;!-- Put in related anions e.g, iron(II) fluoride &amp;amp; iron(II) bromide if compound is iron(II) chloride --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| Other [[Ion|cation]]s &amp;lt;!-- please omit if not applicable --&amp;gt;&lt;br /&gt;
| {{{Ohter_cation}}} &amp;lt;!-- Put in other oxidation states of same element e.g. [[iron(III) chloride]], also for related metals such as [[manganese(II) chloride]], [[cobalt(II) chloride]], ruthenium(III) chloride--&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| Related compounds &lt;br /&gt;
&amp;lt;!-- A miscellaneous heading - use for covalent inorganics;  e.g. for PCl&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt; you would list PCl&amp;lt;sub&amp;gt;5&amp;lt;/sub&amp;gt;, POCl&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;, PF&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;, PBr&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;, NCl&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt; and AsCl&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;. &lt;br /&gt;
Please omit if not applicable --&amp;gt;&lt;br /&gt;
| {{{Relative_Compounds}}}&lt;br /&gt;
|-&lt;br /&gt;
| {{chembox header}} | &amp;lt;small&amp;gt;Except where noted otherwise, data are given for&amp;lt;br /&amp;gt; materials in their [[standard state|standard state (at 25&amp;amp;nbsp;°C, 100&amp;amp;nbsp;kPa)]]&amp;lt;br /&amp;gt;[[wikipedia:Chemical infobox|Infobox disclaimer and references]]&amp;lt;/small&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
|}&lt;br /&gt;
{{Chem-Data_Structure}}&lt;/div&gt;</summary>
		<author><name>Wwl06</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=Rohypnol&amp;diff=12075</id>
		<title>Rohypnol</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=Rohypnol&amp;diff=12075"/>
		<updated>2007-11-27T15:38:38Z</updated>

		<summary type="html">&lt;p&gt;Wwl06: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&amp;lt;noinclude&amp;gt;&lt;br /&gt;
&amp;lt;!-- This template has been defined after elaborate discussion in the Chemicals Wikiproject. Please do not add, deleted or otherwise change it unless after due discussion in [[wikipedia talk:WikiProject Chemicals]] --&amp;gt;&lt;br /&gt;
&amp;lt;/noinclude&amp;gt;{| class=&amp;quot;toccolours&amp;quot; border=&amp;quot;1&amp;quot; style=&amp;quot;float: right; clear: right; margin: 0 0 1em 1em; border-collapse: collapse; width: 280px&amp;quot;&lt;br /&gt;
! {{chembox header}} | {{PAGENAME}} &amp;lt;!-- replace if not identical with the article name --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image:{{PAGENAME}}.jpg|200px|{{PAGENAME}}]] &amp;lt;!-- replace if not identical with the pagename --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | General&lt;br /&gt;
|- &lt;br /&gt;
| [http://en.wikipedia.org/wiki/IUPAC Systematic name]&lt;br /&gt;
| 6-(2-fluorophenyl)-2-methyl-9-nitro-2,&lt;br /&gt;
5-diazabicyclo[5.4.0]undeca-5,8,10,12-&lt;br /&gt;
tetraen-3-one&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
| Other names&lt;br /&gt;
| {{{OtherNames}}}&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Chemical_formula Molecular formula]&lt;br /&gt;
| C16H12FN3O3&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Molar_mass Molar mass]&lt;br /&gt;
| 313.3&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
| Appearance&lt;br /&gt;
| White, light yellow crystalline powder&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/CAS_registry_number CAS number]&lt;br /&gt;
| 1622-62-4&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Properties&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Density Density] &amp;amp; [http://en.wikipedia.org/wiki/Phase_%28matter%29 phase]&lt;br /&gt;
| {{{Density}}} g/cm³ &amp;lt;!-- ? g/cm³, solid / ? g/ml, liquid / ? g/l, gas --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Solubility Solubility]&lt;br /&gt;
| Almost insoluble in water but soluble in alcohol&amp;lt;!--  at least put miscible with, not soluble in --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
&amp;lt;!-- | Other solvents e.g. [[ethanol]], [[acetone]] --&amp;gt;&lt;br /&gt;
&amp;lt;!-- | solubility info on other solvents --&amp;gt;&lt;br /&gt;
&amp;lt;!-- |- --&amp;gt;&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Melting_point Melting point]&lt;br /&gt;
| 168-172 C &amp;lt;!-- (mention any decomposition) --&amp;gt;&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Structure&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Orbital_hybridisation Molecular shape] &amp;lt;!-- for simple covalent molecules (omit for most large molecules, ionics and complexes) --&amp;gt;&lt;br /&gt;
| {{{Mol_Shape}}} &amp;lt;!-- e.g. trigonal bipyramidal --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Coordination_geometry Coordination&amp;lt;br /&amp;gt;geometry] &amp;lt;!-- for a metal complex or an ionic crystal, otherwise omit --&amp;gt;&lt;br /&gt;
| {{{Coordination}}} &amp;lt;!-- e.g. trigonal bipyramidal --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Crystal_structure Crystal structure] &amp;lt;!-- omit if not a solid --&amp;gt;&lt;br /&gt;
| {{{Crystal_Structure}}} &amp;lt;!-- e.g. [[triclinic]], [[monoclinic]], [[orthorhombic]], [[hexagonal]], [[rhombohedral|trigonal]], [[tetragonal]], [[cubic]], and mention &amp;quot;close packed&amp;quot; or similar.  You may also cite what class it belongs to, e.g. [[Cadmium_chloride#Crystal_structure|CdCl&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt;]]  --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [[Dipole#Molecular_dipoles|Dipole moment]]&lt;br /&gt;
| {{{DM}}} [[Debye|D]]&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Hazards &amp;lt;!--  Summary only- MSDS entry provides more complete information --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [[Material safety data sheet|MSDS]]&lt;br /&gt;
| [[{{PAGENAME}} (data page)#Material Safety Data Sheet|External MSDS]] &amp;lt;!-- please replace with proper link--&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| Main [[Worker safety and health|hazard]]s&lt;br /&gt;
| {{{Hazards}}} &amp;lt;!-- e.g. highly toxic, explosive, flammable, corrosive --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [[NFPA 704]]&lt;br /&gt;
| {{{NFPA}}}&amp;lt;!-- {{NFPA 704 | Health=4 | Flammability=4 | Reactivity=4 | Other=OX }} These are set on &amp;quot;very dangerous&amp;quot; as default- adjust according to actual values --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [[Flash point]]&lt;br /&gt;
| {{{Fp}}}°C&lt;br /&gt;
|-&lt;br /&gt;
| [[Risk and Safety Statements|R/S statement]]&lt;br /&gt;
| [[List of R-phrases|R]]: {{{R-S}}} &amp;lt;br /&amp;gt; [[List of S-phrases|S]]: ?&lt;br /&gt;
|-&lt;br /&gt;
| [[RTECS]] number&lt;br /&gt;
| {{{RTECS}}}&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | [[{{PAGENAME}} (data page)|Supplementary data page]]&lt;br /&gt;
|-&lt;br /&gt;
| [[{{PAGENAME}} (data page)#Structure and properties|Structure and&amp;lt;br /&amp;gt;properties]] &lt;br /&gt;
| [http://en.wikipedia.org/wiki/Refractive_index &#039;&#039;n&#039;&#039;], [http://en.wikipedia.org/wiki/Dielectric_constant ε&amp;lt;sub&amp;gt;r&amp;lt;/sub&amp;gt;], etc. &lt;br /&gt;
|-&lt;br /&gt;
| [[{{PAGENAME}} (data page)#Thermodynamic properties|Thermodynamic&amp;lt;br /&amp;gt;data]] &lt;br /&gt;
| Phase behaviour&amp;lt;br /&amp;gt;Solid, liquid, gas &lt;br /&gt;
|-&lt;br /&gt;
| [[{{PAGENAME}} (data page)#Spectral data|Spectral data]]&lt;br /&gt;
| [[UV/VIS spectroscopy|UV]], [[Infrared spectroscopy|IR]], [[nuclear magnetic resonance spectroscopy|NMR]], [[Mass spectrometry|MS]]&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Related compounds&lt;br /&gt;
|-&lt;br /&gt;
| Other [[Ion|anion]]s &amp;lt;!-- please omit if not applicable --&amp;gt;&lt;br /&gt;
| {{{Other_anion}}} &amp;lt;!-- Put in related anions e.g, iron(II) fluoride &amp;amp; iron(II) bromide if compound is iron(II) chloride --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| Other [[Ion|cation]]s &amp;lt;!-- please omit if not applicable --&amp;gt;&lt;br /&gt;
| {{{Ohter_cation}}} &amp;lt;!-- Put in other oxidation states of same element e.g. [[iron(III) chloride]], also for related metals such as [[manganese(II) chloride]], [[cobalt(II) chloride]], ruthenium(III) chloride--&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| Related compounds &lt;br /&gt;
&amp;lt;!-- A miscellaneous heading - use for covalent inorganics;  e.g. for PCl&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt; you would list PCl&amp;lt;sub&amp;gt;5&amp;lt;/sub&amp;gt;, POCl&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;, PF&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;, PBr&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;, NCl&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt; and AsCl&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;. &lt;br /&gt;
Please omit if not applicable --&amp;gt;&lt;br /&gt;
| {{{Relative_Compounds}}}&lt;br /&gt;
|-&lt;br /&gt;
| {{chembox header}} | &amp;lt;small&amp;gt;Except where noted otherwise, data are given for&amp;lt;br /&amp;gt; materials in their [[standard state|standard state (at 25&amp;amp;nbsp;°C, 100&amp;amp;nbsp;kPa)]]&amp;lt;br /&amp;gt;[[wikipedia:Chemical infobox|Infobox disclaimer and references]]&amp;lt;/small&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
|}&lt;br /&gt;
{{Chem-Data_Structure}}&lt;/div&gt;</summary>
		<author><name>Wwl06</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=Rohypnol&amp;diff=12072</id>
		<title>Rohypnol</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=Rohypnol&amp;diff=12072"/>
		<updated>2007-11-27T15:38:02Z</updated>

		<summary type="html">&lt;p&gt;Wwl06: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&amp;lt;noinclude&amp;gt;&lt;br /&gt;
&amp;lt;!-- This template has been defined after elaborate discussion in the Chemicals Wikiproject. Please do not add, deleted or otherwise change it unless after due discussion in [[wikipedia talk:WikiProject Chemicals]] --&amp;gt;&lt;br /&gt;
&amp;lt;/noinclude&amp;gt;{| class=&amp;quot;toccolours&amp;quot; border=&amp;quot;1&amp;quot; style=&amp;quot;float: right; clear: right; margin: 0 0 1em 1em; border-collapse: collapse; width: 280px&amp;quot;&lt;br /&gt;
! {{chembox header}} | {{PAGENAME}} &amp;lt;!-- replace if not identical with the article name --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image:{{PAGENAME}}.jpg|200px|{{PAGENAME}}]] &amp;lt;!-- replace if not identical with the pagename --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | General&lt;br /&gt;
|- &lt;br /&gt;
| [http://en.wikipedia.org/wiki/IUPAC Systematic name]&lt;br /&gt;
| 6-(2-fluorophenyl)-2-methyl-9-nitro-2,&lt;br /&gt;
5-diazabicyclo[5.4.0]undeca-5,8,10,12-&lt;br /&gt;
tetraen-3-one&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
| Other names&lt;br /&gt;
| {{{OtherNames}}}&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Chemical_formula Molecular formula]&lt;br /&gt;
| C16H12FN3O3&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Molar_mass Molar mass]&lt;br /&gt;
| 313.3&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
| Appearance&lt;br /&gt;
| White, light yellow crystalline powder&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/CAS_registry_number CAS number]&lt;br /&gt;
| 1622-62-4&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Properties&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Density Density] &amp;amp; [http://en.wikipedia.org/wiki/Phase_%28matter%29 phase]&lt;br /&gt;
| {{{Density}}} g/cm³ &amp;lt;!-- ? g/cm³, solid / ? g/ml, liquid / ? g/l, gas --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Solubility Solubility]&lt;br /&gt;
| Almost insoluble in water but soluble in alcohol&amp;lt;!--  at least put miscible with, not soluble in --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
&amp;lt;!-- | Other solvents e.g. [[ethanol]], [[acetone]] --&amp;gt;&lt;br /&gt;
&amp;lt;!-- | solubility info on other solvents --&amp;gt;&lt;br /&gt;
&amp;lt;!-- |- --&amp;gt;&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Melting_point Melting point]&lt;br /&gt;
| 168-172 C &amp;lt;!-- (mention any decomposition) --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Boiling_point Boiling point]&lt;br /&gt;
| {{{Bp}}} K&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Acid_dissociation_constant Acidity] (p&#039;&#039;K&#039;&#039;&amp;lt;sub&amp;gt;a&amp;lt;/sub&amp;gt;) &amp;lt;!-- omit if not an acid or a base.  If several values, be clear --&amp;gt;&lt;br /&gt;
| {{{pKa}}}&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Acid_dissociation_constant Basicity] (p&#039;&#039;K&#039;&#039;&amp;lt;sub&amp;gt;b&amp;lt;/sub&amp;gt;) &amp;lt;!-- omit if not a base. If several values, be clear --&amp;gt;&lt;br /&gt;
| {{{pKb}}}&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Specific_rotation Chiral rotation &amp;lt;nowiki&amp;gt;[α]&amp;lt;/nowiki&amp;gt;&amp;lt;sub&amp;gt;D&amp;lt;/sub&amp;gt;] &amp;lt;!-- (Only include this for chiral compounds, indicate direction/enantiomer combo if known) --&amp;gt;&lt;br /&gt;
| {{{Rotation}}}°&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Viscosity Viscosity]&lt;br /&gt;
| {{{Viscosity}}} [[Poise|cP]] at 25°C &amp;lt;!-- Liquids only, omit if data unavailable. You may use [[Pascal second|Pa.s]] if you prefer --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Structure&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Orbital_hybridisation Molecular shape] &amp;lt;!-- for simple covalent molecules (omit for most large molecules, ionics and complexes) --&amp;gt;&lt;br /&gt;
| {{{Mol_Shape}}} &amp;lt;!-- e.g. trigonal bipyramidal --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Coordination_geometry Coordination&amp;lt;br /&amp;gt;geometry] &amp;lt;!-- for a metal complex or an ionic crystal, otherwise omit --&amp;gt;&lt;br /&gt;
| {{{Coordination}}} &amp;lt;!-- e.g. trigonal bipyramidal --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Crystal_structure Crystal structure] &amp;lt;!-- omit if not a solid --&amp;gt;&lt;br /&gt;
| {{{Crystal_Structure}}} &amp;lt;!-- e.g. [[triclinic]], [[monoclinic]], [[orthorhombic]], [[hexagonal]], [[rhombohedral|trigonal]], [[tetragonal]], [[cubic]], and mention &amp;quot;close packed&amp;quot; or similar.  You may also cite what class it belongs to, e.g. [[Cadmium_chloride#Crystal_structure|CdCl&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt;]]  --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [[Dipole#Molecular_dipoles|Dipole moment]]&lt;br /&gt;
| {{{DM}}} [[Debye|D]]&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Hazards &amp;lt;!--  Summary only- MSDS entry provides more complete information --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [[Material safety data sheet|MSDS]]&lt;br /&gt;
| [[{{PAGENAME}} (data page)#Material Safety Data Sheet|External MSDS]] &amp;lt;!-- please replace with proper link--&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| Main [[Worker safety and health|hazard]]s&lt;br /&gt;
| {{{Hazards}}} &amp;lt;!-- e.g. highly toxic, explosive, flammable, corrosive --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [[NFPA 704]]&lt;br /&gt;
| {{{NFPA}}}&amp;lt;!-- {{NFPA 704 | Health=4 | Flammability=4 | Reactivity=4 | Other=OX }} These are set on &amp;quot;very dangerous&amp;quot; as default- adjust according to actual values --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [[Flash point]]&lt;br /&gt;
| {{{Fp}}}°C&lt;br /&gt;
|-&lt;br /&gt;
| [[Risk and Safety Statements|R/S statement]]&lt;br /&gt;
| [[List of R-phrases|R]]: {{{R-S}}} &amp;lt;br /&amp;gt; [[List of S-phrases|S]]: ?&lt;br /&gt;
|-&lt;br /&gt;
| [[RTECS]] number&lt;br /&gt;
| {{{RTECS}}}&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | [[{{PAGENAME}} (data page)|Supplementary data page]]&lt;br /&gt;
|-&lt;br /&gt;
| [[{{PAGENAME}} (data page)#Structure and properties|Structure and&amp;lt;br /&amp;gt;properties]] &lt;br /&gt;
| [http://en.wikipedia.org/wiki/Refractive_index &#039;&#039;n&#039;&#039;], [http://en.wikipedia.org/wiki/Dielectric_constant ε&amp;lt;sub&amp;gt;r&amp;lt;/sub&amp;gt;], etc. &lt;br /&gt;
|-&lt;br /&gt;
| [[{{PAGENAME}} (data page)#Thermodynamic properties|Thermodynamic&amp;lt;br /&amp;gt;data]] &lt;br /&gt;
| Phase behaviour&amp;lt;br /&amp;gt;Solid, liquid, gas &lt;br /&gt;
|-&lt;br /&gt;
| [[{{PAGENAME}} (data page)#Spectral data|Spectral data]]&lt;br /&gt;
| [[UV/VIS spectroscopy|UV]], [[Infrared spectroscopy|IR]], [[nuclear magnetic resonance spectroscopy|NMR]], [[Mass spectrometry|MS]]&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Related compounds&lt;br /&gt;
|-&lt;br /&gt;
| Other [[Ion|anion]]s &amp;lt;!-- please omit if not applicable --&amp;gt;&lt;br /&gt;
| {{{Other_anion}}} &amp;lt;!-- Put in related anions e.g, iron(II) fluoride &amp;amp; iron(II) bromide if compound is iron(II) chloride --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| Other [[Ion|cation]]s &amp;lt;!-- please omit if not applicable --&amp;gt;&lt;br /&gt;
| {{{Ohter_cation}}} &amp;lt;!-- Put in other oxidation states of same element e.g. [[iron(III) chloride]], also for related metals such as [[manganese(II) chloride]], [[cobalt(II) chloride]], ruthenium(III) chloride--&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| Related compounds &lt;br /&gt;
&amp;lt;!-- A miscellaneous heading - use for covalent inorganics;  e.g. for PCl&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt; you would list PCl&amp;lt;sub&amp;gt;5&amp;lt;/sub&amp;gt;, POCl&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;, PF&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;, PBr&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;, NCl&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt; and AsCl&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;. &lt;br /&gt;
Please omit if not applicable --&amp;gt;&lt;br /&gt;
| {{{Relative_Compounds}}}&lt;br /&gt;
|-&lt;br /&gt;
| {{chembox header}} | &amp;lt;small&amp;gt;Except where noted otherwise, data are given for&amp;lt;br /&amp;gt; materials in their [[standard state|standard state (at 25&amp;amp;nbsp;°C, 100&amp;amp;nbsp;kPa)]]&amp;lt;br /&amp;gt;[[wikipedia:Chemical infobox|Infobox disclaimer and references]]&amp;lt;/small&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
|}&lt;br /&gt;
{{Chem-Data_Structure}}&lt;/div&gt;</summary>
		<author><name>Wwl06</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=Rohypnol&amp;diff=12070</id>
		<title>Rohypnol</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=Rohypnol&amp;diff=12070"/>
		<updated>2007-11-27T15:34:53Z</updated>

		<summary type="html">&lt;p&gt;Wwl06: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&amp;lt;noinclude&amp;gt;&lt;br /&gt;
&amp;lt;!-- This template has been defined after elaborate discussion in the Chemicals Wikiproject. Please do not add, deleted or otherwise change it unless after due discussion in [[wikipedia talk:WikiProject Chemicals]] --&amp;gt;&lt;br /&gt;
&amp;lt;/noinclude&amp;gt;{| class=&amp;quot;toccolours&amp;quot; border=&amp;quot;1&amp;quot; style=&amp;quot;float: right; clear: right; margin: 0 0 1em 1em; border-collapse: collapse; width: 280px&amp;quot;&lt;br /&gt;
! {{chembox header}} | {{PAGENAME}} &amp;lt;!-- replace if not identical with the article name --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image:{{PAGENAME}}.jpg|200px|{{PAGENAME}}]] &amp;lt;!-- replace if not identical with the pagename --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | General&lt;br /&gt;
|- &lt;br /&gt;
| [http://en.wikipedia.org/wiki/IUPAC Systematic name]&lt;br /&gt;
| 6-(2-fluorophenyl)-2-methyl-9-nitro-2,&lt;br /&gt;
5-diazabicyclo[5.4.0]undeca-5,8,10,12-&lt;br /&gt;
tetraen-3-one&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
| Other names&lt;br /&gt;
| {{{OtherNames}}}&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Chemical_formula Molecular formula]&lt;br /&gt;
| C16H12FN3O3&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Molar_mass Molar mass]&lt;br /&gt;
| 313.3&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
| Appearance&lt;br /&gt;
| White, light yellow crystalline powder&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/CAS_registry_number CAS number]&lt;br /&gt;
| {{{CASNo}}}&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Properties&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Density Density] &amp;amp; [http://en.wikipedia.org/wiki/Phase_%28matter%29 phase]&lt;br /&gt;
| {{{Density}}} g/cm³ &amp;lt;!-- ? g/cm³, solid / ? g/ml, liquid / ? g/l, gas --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Solubility Solubility]&lt;br /&gt;
| Almost insoluble in water but soluble in alcohol&amp;lt;!--  at least put miscible with, not soluble in --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
&amp;lt;!-- | Other solvents e.g. [[ethanol]], [[acetone]] --&amp;gt;&lt;br /&gt;
&amp;lt;!-- | solubility info on other solvents --&amp;gt;&lt;br /&gt;
&amp;lt;!-- |- --&amp;gt;&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Melting_point Melting point]&lt;br /&gt;
| 168-172 C &amp;lt;!-- (mention any decomposition) --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Boiling_point Boiling point]&lt;br /&gt;
| {{{Bp}}} K&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Acid_dissociation_constant Acidity] (p&#039;&#039;K&#039;&#039;&amp;lt;sub&amp;gt;a&amp;lt;/sub&amp;gt;) &amp;lt;!-- omit if not an acid or a base.  If several values, be clear --&amp;gt;&lt;br /&gt;
| {{{pKa}}}&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Acid_dissociation_constant Basicity] (p&#039;&#039;K&#039;&#039;&amp;lt;sub&amp;gt;b&amp;lt;/sub&amp;gt;) &amp;lt;!-- omit if not a base. If several values, be clear --&amp;gt;&lt;br /&gt;
| {{{pKb}}}&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Specific_rotation Chiral rotation &amp;lt;nowiki&amp;gt;[α]&amp;lt;/nowiki&amp;gt;&amp;lt;sub&amp;gt;D&amp;lt;/sub&amp;gt;] &amp;lt;!-- (Only include this for chiral compounds, indicate direction/enantiomer combo if known) --&amp;gt;&lt;br /&gt;
| {{{Rotation}}}°&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Viscosity Viscosity]&lt;br /&gt;
| {{{Viscosity}}} [[Poise|cP]] at 25°C &amp;lt;!-- Liquids only, omit if data unavailable. You may use [[Pascal second|Pa.s]] if you prefer --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Structure&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Orbital_hybridisation Molecular shape] &amp;lt;!-- for simple covalent molecules (omit for most large molecules, ionics and complexes) --&amp;gt;&lt;br /&gt;
| {{{Mol_Shape}}} &amp;lt;!-- e.g. trigonal bipyramidal --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Coordination_geometry Coordination&amp;lt;br /&amp;gt;geometry] &amp;lt;!-- for a metal complex or an ionic crystal, otherwise omit --&amp;gt;&lt;br /&gt;
| {{{Coordination}}} &amp;lt;!-- e.g. trigonal bipyramidal --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Crystal_structure Crystal structure] &amp;lt;!-- omit if not a solid --&amp;gt;&lt;br /&gt;
| {{{Crystal_Structure}}} &amp;lt;!-- e.g. [[triclinic]], [[monoclinic]], [[orthorhombic]], [[hexagonal]], [[rhombohedral|trigonal]], [[tetragonal]], [[cubic]], and mention &amp;quot;close packed&amp;quot; or similar.  You may also cite what class it belongs to, e.g. [[Cadmium_chloride#Crystal_structure|CdCl&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt;]]  --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [[Dipole#Molecular_dipoles|Dipole moment]]&lt;br /&gt;
| {{{DM}}} [[Debye|D]]&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Hazards &amp;lt;!--  Summary only- MSDS entry provides more complete information --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [[Material safety data sheet|MSDS]]&lt;br /&gt;
| [[{{PAGENAME}} (data page)#Material Safety Data Sheet|External MSDS]] &amp;lt;!-- please replace with proper link--&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| Main [[Worker safety and health|hazard]]s&lt;br /&gt;
| {{{Hazards}}} &amp;lt;!-- e.g. highly toxic, explosive, flammable, corrosive --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [[NFPA 704]]&lt;br /&gt;
| {{{NFPA}}}&amp;lt;!-- {{NFPA 704 | Health=4 | Flammability=4 | Reactivity=4 | Other=OX }} These are set on &amp;quot;very dangerous&amp;quot; as default- adjust according to actual values --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [[Flash point]]&lt;br /&gt;
| {{{Fp}}}°C&lt;br /&gt;
|-&lt;br /&gt;
| [[Risk and Safety Statements|R/S statement]]&lt;br /&gt;
| [[List of R-phrases|R]]: {{{R-S}}} &amp;lt;br /&amp;gt; [[List of S-phrases|S]]: ?&lt;br /&gt;
|-&lt;br /&gt;
| [[RTECS]] number&lt;br /&gt;
| {{{RTECS}}}&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | [[{{PAGENAME}} (data page)|Supplementary data page]]&lt;br /&gt;
|-&lt;br /&gt;
| [[{{PAGENAME}} (data page)#Structure and properties|Structure and&amp;lt;br /&amp;gt;properties]] &lt;br /&gt;
| [http://en.wikipedia.org/wiki/Refractive_index &#039;&#039;n&#039;&#039;], [http://en.wikipedia.org/wiki/Dielectric_constant ε&amp;lt;sub&amp;gt;r&amp;lt;/sub&amp;gt;], etc. &lt;br /&gt;
|-&lt;br /&gt;
| [[{{PAGENAME}} (data page)#Thermodynamic properties|Thermodynamic&amp;lt;br /&amp;gt;data]] &lt;br /&gt;
| Phase behaviour&amp;lt;br /&amp;gt;Solid, liquid, gas &lt;br /&gt;
|-&lt;br /&gt;
| [[{{PAGENAME}} (data page)#Spectral data|Spectral data]]&lt;br /&gt;
| [[UV/VIS spectroscopy|UV]], [[Infrared spectroscopy|IR]], [[nuclear magnetic resonance spectroscopy|NMR]], [[Mass spectrometry|MS]]&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Related compounds&lt;br /&gt;
|-&lt;br /&gt;
| Other [[Ion|anion]]s &amp;lt;!-- please omit if not applicable --&amp;gt;&lt;br /&gt;
| {{{Other_anion}}} &amp;lt;!-- Put in related anions e.g, iron(II) fluoride &amp;amp; iron(II) bromide if compound is iron(II) chloride --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| Other [[Ion|cation]]s &amp;lt;!-- please omit if not applicable --&amp;gt;&lt;br /&gt;
| {{{Ohter_cation}}} &amp;lt;!-- Put in other oxidation states of same element e.g. [[iron(III) chloride]], also for related metals such as [[manganese(II) chloride]], [[cobalt(II) chloride]], ruthenium(III) chloride--&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| Related compounds &lt;br /&gt;
&amp;lt;!-- A miscellaneous heading - use for covalent inorganics;  e.g. for PCl&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt; you would list PCl&amp;lt;sub&amp;gt;5&amp;lt;/sub&amp;gt;, POCl&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;, PF&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;, PBr&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;, NCl&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt; and AsCl&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;. &lt;br /&gt;
Please omit if not applicable --&amp;gt;&lt;br /&gt;
| {{{Relative_Compounds}}}&lt;br /&gt;
|-&lt;br /&gt;
| {{chembox header}} | &amp;lt;small&amp;gt;Except where noted otherwise, data are given for&amp;lt;br /&amp;gt; materials in their [[standard state|standard state (at 25&amp;amp;nbsp;°C, 100&amp;amp;nbsp;kPa)]]&amp;lt;br /&amp;gt;[[wikipedia:Chemical infobox|Infobox disclaimer and references]]&amp;lt;/small&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
|}&lt;br /&gt;
{{Chem-Data_Structure}}&lt;/div&gt;</summary>
		<author><name>Wwl06</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=Rohypnol&amp;diff=12069</id>
		<title>Rohypnol</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=Rohypnol&amp;diff=12069"/>
		<updated>2007-11-27T15:33:33Z</updated>

		<summary type="html">&lt;p&gt;Wwl06: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&amp;lt;noinclude&amp;gt;&lt;br /&gt;
&amp;lt;!-- This template has been defined after elaborate discussion in the Chemicals Wikiproject. Please do not add, deleted or otherwise change it unless after due discussion in [[wikipedia talk:WikiProject Chemicals]] --&amp;gt;&lt;br /&gt;
&amp;lt;/noinclude&amp;gt;{| class=&amp;quot;toccolours&amp;quot; border=&amp;quot;1&amp;quot; style=&amp;quot;float: right; clear: right; margin: 0 0 1em 1em; border-collapse: collapse; width: 280px&amp;quot;&lt;br /&gt;
! {{chembox header}} | {{PAGENAME}} &amp;lt;!-- replace if not identical with the article name --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image:{{PAGENAME}}.jpg|200px|{{PAGENAME}}]] &amp;lt;!-- replace if not identical with the pagename --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | General&lt;br /&gt;
|- &lt;br /&gt;
| [http://en.wikipedia.org/wiki/IUPAC Systematic name]&lt;br /&gt;
| 6-(2-fluorophenyl)-2-methyl-9-nitro-2,&lt;br /&gt;
5-diazabicyclo[5.4.0]undeca-5,8,10,12-&lt;br /&gt;
tetraen-3-one&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
| Other names&lt;br /&gt;
| {{{OtherNames}}}&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Chemical_formula Molecular formula]&lt;br /&gt;
| C16H12FN3O3&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Molar_mass Molar mass]&lt;br /&gt;
| 313.3&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
| Appearance&lt;br /&gt;
| White solid&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/CAS_registry_number CAS number]&lt;br /&gt;
| {{{CASNo}}}&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Properties&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Density Density] &amp;amp; [http://en.wikipedia.org/wiki/Phase_%28matter%29 phase]&lt;br /&gt;
| {{{Density}}} g/cm³ &amp;lt;!-- ? g/cm³, solid / ? g/ml, liquid / ? g/l, gas --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Solubility Solubility]&lt;br /&gt;
| Almost insoluble in water but soluble in alcohol&amp;lt;!--  at least put miscible with, not soluble in --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
&amp;lt;!-- | Other solvents e.g. [[ethanol]], [[acetone]] --&amp;gt;&lt;br /&gt;
&amp;lt;!-- | solubility info on other solvents --&amp;gt;&lt;br /&gt;
&amp;lt;!-- |- --&amp;gt;&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Melting_point Melting point]&lt;br /&gt;
| 168-172 C &amp;lt;!-- (mention any decomposition) --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Boiling_point Boiling point]&lt;br /&gt;
| {{{Bp}}} K&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Acid_dissociation_constant Acidity] (p&#039;&#039;K&#039;&#039;&amp;lt;sub&amp;gt;a&amp;lt;/sub&amp;gt;) &amp;lt;!-- omit if not an acid or a base.  If several values, be clear --&amp;gt;&lt;br /&gt;
| {{{pKa}}}&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Acid_dissociation_constant Basicity] (p&#039;&#039;K&#039;&#039;&amp;lt;sub&amp;gt;b&amp;lt;/sub&amp;gt;) &amp;lt;!-- omit if not a base. If several values, be clear --&amp;gt;&lt;br /&gt;
| {{{pKb}}}&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Specific_rotation Chiral rotation &amp;lt;nowiki&amp;gt;[α]&amp;lt;/nowiki&amp;gt;&amp;lt;sub&amp;gt;D&amp;lt;/sub&amp;gt;] &amp;lt;!-- (Only include this for chiral compounds, indicate direction/enantiomer combo if known) --&amp;gt;&lt;br /&gt;
| {{{Rotation}}}°&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Viscosity Viscosity]&lt;br /&gt;
| {{{Viscosity}}} [[Poise|cP]] at 25°C &amp;lt;!-- Liquids only, omit if data unavailable. You may use [[Pascal second|Pa.s]] if you prefer --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Structure&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Orbital_hybridisation Molecular shape] &amp;lt;!-- for simple covalent molecules (omit for most large molecules, ionics and complexes) --&amp;gt;&lt;br /&gt;
| {{{Mol_Shape}}} &amp;lt;!-- e.g. trigonal bipyramidal --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Coordination_geometry Coordination&amp;lt;br /&amp;gt;geometry] &amp;lt;!-- for a metal complex or an ionic crystal, otherwise omit --&amp;gt;&lt;br /&gt;
| {{{Coordination}}} &amp;lt;!-- e.g. trigonal bipyramidal --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Crystal_structure Crystal structure] &amp;lt;!-- omit if not a solid --&amp;gt;&lt;br /&gt;
| {{{Crystal_Structure}}} &amp;lt;!-- e.g. [[triclinic]], [[monoclinic]], [[orthorhombic]], [[hexagonal]], [[rhombohedral|trigonal]], [[tetragonal]], [[cubic]], and mention &amp;quot;close packed&amp;quot; or similar.  You may also cite what class it belongs to, e.g. [[Cadmium_chloride#Crystal_structure|CdCl&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt;]]  --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [[Dipole#Molecular_dipoles|Dipole moment]]&lt;br /&gt;
| {{{DM}}} [[Debye|D]]&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Hazards &amp;lt;!--  Summary only- MSDS entry provides more complete information --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [[Material safety data sheet|MSDS]]&lt;br /&gt;
| [[{{PAGENAME}} (data page)#Material Safety Data Sheet|External MSDS]] &amp;lt;!-- please replace with proper link--&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| Main [[Worker safety and health|hazard]]s&lt;br /&gt;
| {{{Hazards}}} &amp;lt;!-- e.g. highly toxic, explosive, flammable, corrosive --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [[NFPA 704]]&lt;br /&gt;
| {{{NFPA}}}&amp;lt;!-- {{NFPA 704 | Health=4 | Flammability=4 | Reactivity=4 | Other=OX }} These are set on &amp;quot;very dangerous&amp;quot; as default- adjust according to actual values --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [[Flash point]]&lt;br /&gt;
| {{{Fp}}}°C&lt;br /&gt;
|-&lt;br /&gt;
| [[Risk and Safety Statements|R/S statement]]&lt;br /&gt;
| [[List of R-phrases|R]]: {{{R-S}}} &amp;lt;br /&amp;gt; [[List of S-phrases|S]]: ?&lt;br /&gt;
|-&lt;br /&gt;
| [[RTECS]] number&lt;br /&gt;
| {{{RTECS}}}&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | [[{{PAGENAME}} (data page)|Supplementary data page]]&lt;br /&gt;
|-&lt;br /&gt;
| [[{{PAGENAME}} (data page)#Structure and properties|Structure and&amp;lt;br /&amp;gt;properties]] &lt;br /&gt;
| [http://en.wikipedia.org/wiki/Refractive_index &#039;&#039;n&#039;&#039;], [http://en.wikipedia.org/wiki/Dielectric_constant ε&amp;lt;sub&amp;gt;r&amp;lt;/sub&amp;gt;], etc. &lt;br /&gt;
|-&lt;br /&gt;
| [[{{PAGENAME}} (data page)#Thermodynamic properties|Thermodynamic&amp;lt;br /&amp;gt;data]] &lt;br /&gt;
| Phase behaviour&amp;lt;br /&amp;gt;Solid, liquid, gas &lt;br /&gt;
|-&lt;br /&gt;
| [[{{PAGENAME}} (data page)#Spectral data|Spectral data]]&lt;br /&gt;
| [[UV/VIS spectroscopy|UV]], [[Infrared spectroscopy|IR]], [[nuclear magnetic resonance spectroscopy|NMR]], [[Mass spectrometry|MS]]&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Related compounds&lt;br /&gt;
|-&lt;br /&gt;
| Other [[Ion|anion]]s &amp;lt;!-- please omit if not applicable --&amp;gt;&lt;br /&gt;
| {{{Other_anion}}} &amp;lt;!-- Put in related anions e.g, iron(II) fluoride &amp;amp; iron(II) bromide if compound is iron(II) chloride --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| Other [[Ion|cation]]s &amp;lt;!-- please omit if not applicable --&amp;gt;&lt;br /&gt;
| {{{Ohter_cation}}} &amp;lt;!-- Put in other oxidation states of same element e.g. [[iron(III) chloride]], also for related metals such as [[manganese(II) chloride]], [[cobalt(II) chloride]], ruthenium(III) chloride--&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| Related compounds &lt;br /&gt;
&amp;lt;!-- A miscellaneous heading - use for covalent inorganics;  e.g. for PCl&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt; you would list PCl&amp;lt;sub&amp;gt;5&amp;lt;/sub&amp;gt;, POCl&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;, PF&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;, PBr&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;, NCl&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt; and AsCl&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;. &lt;br /&gt;
Please omit if not applicable --&amp;gt;&lt;br /&gt;
| {{{Relative_Compounds}}}&lt;br /&gt;
|-&lt;br /&gt;
| {{chembox header}} | &amp;lt;small&amp;gt;Except where noted otherwise, data are given for&amp;lt;br /&amp;gt; materials in their [[standard state|standard state (at 25&amp;amp;nbsp;°C, 100&amp;amp;nbsp;kPa)]]&amp;lt;br /&amp;gt;[[wikipedia:Chemical infobox|Infobox disclaimer and references]]&amp;lt;/small&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
|}&lt;br /&gt;
{{Chem-Data_Structure}}&lt;/div&gt;</summary>
		<author><name>Wwl06</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=Rohypnol&amp;diff=12068</id>
		<title>Rohypnol</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=Rohypnol&amp;diff=12068"/>
		<updated>2007-11-27T15:33:12Z</updated>

		<summary type="html">&lt;p&gt;Wwl06: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&amp;lt;noinclude&amp;gt;&lt;br /&gt;
&amp;lt;!-- This template has been defined after elaborate discussion in the Chemicals Wikiproject. Please do not add, deleted or otherwise change it unless after due discussion in [[wikipedia talk:WikiProject Chemicals]] --&amp;gt;&lt;br /&gt;
&amp;lt;/noinclude&amp;gt;{| class=&amp;quot;toccolours&amp;quot; border=&amp;quot;1&amp;quot; style=&amp;quot;float: right; clear: right; margin: 0 0 1em 1em; border-collapse: collapse; width: 280px&amp;quot;&lt;br /&gt;
! {{chembox header}} | {{PAGENAME}} &amp;lt;!-- replace if not identical with the article name --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image:{{PAGENAME}}.jpg|200px|{{PAGENAME}}]] &amp;lt;!-- replace if not identical with the pagename --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | General&lt;br /&gt;
|- &lt;br /&gt;
| [http://en.wikipedia.org/wiki/IUPAC Systematic name]&lt;br /&gt;
| 6-(2-fluorophenyl)-2-methyl-9-nitro-2,&lt;br /&gt;
5-diazabicyclo[5.4.0]undeca-5,8,10,12-&lt;br /&gt;
tetraen-3-one&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
| Other names&lt;br /&gt;
| {{{OtherNames}}}&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Chemical_formula Molecular formula]&lt;br /&gt;
| C16H12FN3O3&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Molar_mass Molar mass]&lt;br /&gt;
| 313.3&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
| Appearance&lt;br /&gt;
| White solid&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/CAS_registry_number CAS number]&lt;br /&gt;
| {{{CASNo}}}&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Properties&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Density Density] &amp;amp; [http://en.wikipedia.org/wiki/Phase_%28matter%29 phase]&lt;br /&gt;
| {{{Density}}} g/cm³ &amp;lt;!-- ? g/cm³, solid / ? g/ml, liquid / ? g/l, gas --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Solubility Solubility]&lt;br /&gt;
| Almost insoluble &amp;lt;!--  at least put miscible with, not soluble in --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
&amp;lt;!-- | Other solvents e.g. [[ethanol]], [[acetone]] --&amp;gt;&lt;br /&gt;
&amp;lt;!-- | solubility info on other solvents --&amp;gt;&lt;br /&gt;
&amp;lt;!-- |- --&amp;gt;&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Melting_point Melting point]&lt;br /&gt;
| 168-172 C &amp;lt;!-- (mention any decomposition) --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Boiling_point Boiling point]&lt;br /&gt;
| {{{Bp}}} K&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Acid_dissociation_constant Acidity] (p&#039;&#039;K&#039;&#039;&amp;lt;sub&amp;gt;a&amp;lt;/sub&amp;gt;) &amp;lt;!-- omit if not an acid or a base.  If several values, be clear --&amp;gt;&lt;br /&gt;
| {{{pKa}}}&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Acid_dissociation_constant Basicity] (p&#039;&#039;K&#039;&#039;&amp;lt;sub&amp;gt;b&amp;lt;/sub&amp;gt;) &amp;lt;!-- omit if not a base. If several values, be clear --&amp;gt;&lt;br /&gt;
| {{{pKb}}}&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Specific_rotation Chiral rotation &amp;lt;nowiki&amp;gt;[α]&amp;lt;/nowiki&amp;gt;&amp;lt;sub&amp;gt;D&amp;lt;/sub&amp;gt;] &amp;lt;!-- (Only include this for chiral compounds, indicate direction/enantiomer combo if known) --&amp;gt;&lt;br /&gt;
| {{{Rotation}}}°&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Viscosity Viscosity]&lt;br /&gt;
| {{{Viscosity}}} [[Poise|cP]] at 25°C &amp;lt;!-- Liquids only, omit if data unavailable. You may use [[Pascal second|Pa.s]] if you prefer --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Structure&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Orbital_hybridisation Molecular shape] &amp;lt;!-- for simple covalent molecules (omit for most large molecules, ionics and complexes) --&amp;gt;&lt;br /&gt;
| {{{Mol_Shape}}} &amp;lt;!-- e.g. trigonal bipyramidal --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Coordination_geometry Coordination&amp;lt;br /&amp;gt;geometry] &amp;lt;!-- for a metal complex or an ionic crystal, otherwise omit --&amp;gt;&lt;br /&gt;
| {{{Coordination}}} &amp;lt;!-- e.g. trigonal bipyramidal --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Crystal_structure Crystal structure] &amp;lt;!-- omit if not a solid --&amp;gt;&lt;br /&gt;
| {{{Crystal_Structure}}} &amp;lt;!-- e.g. [[triclinic]], [[monoclinic]], [[orthorhombic]], [[hexagonal]], [[rhombohedral|trigonal]], [[tetragonal]], [[cubic]], and mention &amp;quot;close packed&amp;quot; or similar.  You may also cite what class it belongs to, e.g. [[Cadmium_chloride#Crystal_structure|CdCl&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt;]]  --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [[Dipole#Molecular_dipoles|Dipole moment]]&lt;br /&gt;
| {{{DM}}} [[Debye|D]]&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Hazards &amp;lt;!--  Summary only- MSDS entry provides more complete information --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [[Material safety data sheet|MSDS]]&lt;br /&gt;
| [[{{PAGENAME}} (data page)#Material Safety Data Sheet|External MSDS]] &amp;lt;!-- please replace with proper link--&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| Main [[Worker safety and health|hazard]]s&lt;br /&gt;
| {{{Hazards}}} &amp;lt;!-- e.g. highly toxic, explosive, flammable, corrosive --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [[NFPA 704]]&lt;br /&gt;
| {{{NFPA}}}&amp;lt;!-- {{NFPA 704 | Health=4 | Flammability=4 | Reactivity=4 | Other=OX }} These are set on &amp;quot;very dangerous&amp;quot; as default- adjust according to actual values --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [[Flash point]]&lt;br /&gt;
| {{{Fp}}}°C&lt;br /&gt;
|-&lt;br /&gt;
| [[Risk and Safety Statements|R/S statement]]&lt;br /&gt;
| [[List of R-phrases|R]]: {{{R-S}}} &amp;lt;br /&amp;gt; [[List of S-phrases|S]]: ?&lt;br /&gt;
|-&lt;br /&gt;
| [[RTECS]] number&lt;br /&gt;
| {{{RTECS}}}&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | [[{{PAGENAME}} (data page)|Supplementary data page]]&lt;br /&gt;
|-&lt;br /&gt;
| [[{{PAGENAME}} (data page)#Structure and properties|Structure and&amp;lt;br /&amp;gt;properties]] &lt;br /&gt;
| [http://en.wikipedia.org/wiki/Refractive_index &#039;&#039;n&#039;&#039;], [http://en.wikipedia.org/wiki/Dielectric_constant ε&amp;lt;sub&amp;gt;r&amp;lt;/sub&amp;gt;], etc. &lt;br /&gt;
|-&lt;br /&gt;
| [[{{PAGENAME}} (data page)#Thermodynamic properties|Thermodynamic&amp;lt;br /&amp;gt;data]] &lt;br /&gt;
| Phase behaviour&amp;lt;br /&amp;gt;Solid, liquid, gas &lt;br /&gt;
|-&lt;br /&gt;
| [[{{PAGENAME}} (data page)#Spectral data|Spectral data]]&lt;br /&gt;
| [[UV/VIS spectroscopy|UV]], [[Infrared spectroscopy|IR]], [[nuclear magnetic resonance spectroscopy|NMR]], [[Mass spectrometry|MS]]&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Related compounds&lt;br /&gt;
|-&lt;br /&gt;
| Other [[Ion|anion]]s &amp;lt;!-- please omit if not applicable --&amp;gt;&lt;br /&gt;
| {{{Other_anion}}} &amp;lt;!-- Put in related anions e.g, iron(II) fluoride &amp;amp; iron(II) bromide if compound is iron(II) chloride --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| Other [[Ion|cation]]s &amp;lt;!-- please omit if not applicable --&amp;gt;&lt;br /&gt;
| {{{Ohter_cation}}} &amp;lt;!-- Put in other oxidation states of same element e.g. [[iron(III) chloride]], also for related metals such as [[manganese(II) chloride]], [[cobalt(II) chloride]], ruthenium(III) chloride--&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| Related compounds &lt;br /&gt;
&amp;lt;!-- A miscellaneous heading - use for covalent inorganics;  e.g. for PCl&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt; you would list PCl&amp;lt;sub&amp;gt;5&amp;lt;/sub&amp;gt;, POCl&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;, PF&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;, PBr&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;, NCl&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt; and AsCl&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;. &lt;br /&gt;
Please omit if not applicable --&amp;gt;&lt;br /&gt;
| {{{Relative_Compounds}}}&lt;br /&gt;
|-&lt;br /&gt;
| {{chembox header}} | &amp;lt;small&amp;gt;Except where noted otherwise, data are given for&amp;lt;br /&amp;gt; materials in their [[standard state|standard state (at 25&amp;amp;nbsp;°C, 100&amp;amp;nbsp;kPa)]]&amp;lt;br /&amp;gt;[[wikipedia:Chemical infobox|Infobox disclaimer and references]]&amp;lt;/small&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
|}&lt;br /&gt;
{{Chem-Data_Structure}}&lt;/div&gt;</summary>
		<author><name>Wwl06</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=Rohypnol&amp;diff=12067</id>
		<title>Rohypnol</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=Rohypnol&amp;diff=12067"/>
		<updated>2007-11-27T15:32:41Z</updated>

		<summary type="html">&lt;p&gt;Wwl06: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&amp;lt;noinclude&amp;gt;&lt;br /&gt;
&amp;lt;!-- This template has been defined after elaborate discussion in the Chemicals Wikiproject. Please do not add, deleted or otherwise change it unless after due discussion in [[wikipedia talk:WikiProject Chemicals]] --&amp;gt;&lt;br /&gt;
&amp;lt;/noinclude&amp;gt;{| class=&amp;quot;toccolours&amp;quot; border=&amp;quot;1&amp;quot; style=&amp;quot;float: right; clear: right; margin: 0 0 1em 1em; border-collapse: collapse; width: 280px&amp;quot;&lt;br /&gt;
! {{chembox header}} | {{PAGENAME}} &amp;lt;!-- replace if not identical with the article name --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image:{{PAGENAME}}.jpg|200px|{{PAGENAME}}]] &amp;lt;!-- replace if not identical with the pagename --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | General&lt;br /&gt;
|- &lt;br /&gt;
| [http://en.wikipedia.org/wiki/IUPAC Systematic name]&lt;br /&gt;
| 6-(2-fluorophenyl)-2-methyl-9-nitro-2,&lt;br /&gt;
5-diazabicyclo[5.4.0]undeca-5,8,10,12-&lt;br /&gt;
tetraen-3-one&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
| Other names&lt;br /&gt;
| {{{OtherNames}}}&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Chemical_formula Molecular formula]&lt;br /&gt;
| C16H12FN3O3&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Molar_mass Molar mass]&lt;br /&gt;
| 313.3&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
| Appearance&lt;br /&gt;
| White solid&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/CAS_registry_number CAS number]&lt;br /&gt;
| {{{CASNo}}}&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Properties&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Density Density] &amp;amp; [http://en.wikipedia.org/wiki/Phase_%28matter%29 phase]&lt;br /&gt;
| {{{Density}}} g/cm³ &amp;lt;!-- ? g/cm³, solid / ? g/ml, liquid / ? g/l, gas --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Solubility Solubility in water]&lt;br /&gt;
| Almost insoluble &amp;lt;!--  at least put miscible with, not soluble in --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
&amp;lt;!-- | Other solvents e.g. [[ethanol]], [[acetone]] --&amp;gt;&lt;br /&gt;
&amp;lt;!-- | solubility info on other solvents --&amp;gt;&lt;br /&gt;
&amp;lt;!-- |- --&amp;gt;&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Melting_point Melting point]&lt;br /&gt;
| 168-172 C &amp;lt;!-- (mention any decomposition) --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Boiling_point Boiling point]&lt;br /&gt;
| {{{Bp}}} K&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Acid_dissociation_constant Acidity] (p&#039;&#039;K&#039;&#039;&amp;lt;sub&amp;gt;a&amp;lt;/sub&amp;gt;) &amp;lt;!-- omit if not an acid or a base.  If several values, be clear --&amp;gt;&lt;br /&gt;
| {{{pKa}}}&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Acid_dissociation_constant Basicity] (p&#039;&#039;K&#039;&#039;&amp;lt;sub&amp;gt;b&amp;lt;/sub&amp;gt;) &amp;lt;!-- omit if not a base. If several values, be clear --&amp;gt;&lt;br /&gt;
| {{{pKb}}}&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Specific_rotation Chiral rotation &amp;lt;nowiki&amp;gt;[α]&amp;lt;/nowiki&amp;gt;&amp;lt;sub&amp;gt;D&amp;lt;/sub&amp;gt;] &amp;lt;!-- (Only include this for chiral compounds, indicate direction/enantiomer combo if known) --&amp;gt;&lt;br /&gt;
| {{{Rotation}}}°&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Viscosity Viscosity]&lt;br /&gt;
| {{{Viscosity}}} [[Poise|cP]] at 25°C &amp;lt;!-- Liquids only, omit if data unavailable. You may use [[Pascal second|Pa.s]] if you prefer --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Structure&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Orbital_hybridisation Molecular shape] &amp;lt;!-- for simple covalent molecules (omit for most large molecules, ionics and complexes) --&amp;gt;&lt;br /&gt;
| {{{Mol_Shape}}} &amp;lt;!-- e.g. trigonal bipyramidal --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Coordination_geometry Coordination&amp;lt;br /&amp;gt;geometry] &amp;lt;!-- for a metal complex or an ionic crystal, otherwise omit --&amp;gt;&lt;br /&gt;
| {{{Coordination}}} &amp;lt;!-- e.g. trigonal bipyramidal --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Crystal_structure Crystal structure] &amp;lt;!-- omit if not a solid --&amp;gt;&lt;br /&gt;
| {{{Crystal_Structure}}} &amp;lt;!-- e.g. [[triclinic]], [[monoclinic]], [[orthorhombic]], [[hexagonal]], [[rhombohedral|trigonal]], [[tetragonal]], [[cubic]], and mention &amp;quot;close packed&amp;quot; or similar.  You may also cite what class it belongs to, e.g. [[Cadmium_chloride#Crystal_structure|CdCl&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt;]]  --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [[Dipole#Molecular_dipoles|Dipole moment]]&lt;br /&gt;
| {{{DM}}} [[Debye|D]]&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Hazards &amp;lt;!--  Summary only- MSDS entry provides more complete information --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [[Material safety data sheet|MSDS]]&lt;br /&gt;
| [[{{PAGENAME}} (data page)#Material Safety Data Sheet|External MSDS]] &amp;lt;!-- please replace with proper link--&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| Main [[Worker safety and health|hazard]]s&lt;br /&gt;
| {{{Hazards}}} &amp;lt;!-- e.g. highly toxic, explosive, flammable, corrosive --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [[NFPA 704]]&lt;br /&gt;
| {{{NFPA}}}&amp;lt;!-- {{NFPA 704 | Health=4 | Flammability=4 | Reactivity=4 | Other=OX }} These are set on &amp;quot;very dangerous&amp;quot; as default- adjust according to actual values --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [[Flash point]]&lt;br /&gt;
| {{{Fp}}}°C&lt;br /&gt;
|-&lt;br /&gt;
| [[Risk and Safety Statements|R/S statement]]&lt;br /&gt;
| [[List of R-phrases|R]]: {{{R-S}}} &amp;lt;br /&amp;gt; [[List of S-phrases|S]]: ?&lt;br /&gt;
|-&lt;br /&gt;
| [[RTECS]] number&lt;br /&gt;
| {{{RTECS}}}&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | [[{{PAGENAME}} (data page)|Supplementary data page]]&lt;br /&gt;
|-&lt;br /&gt;
| [[{{PAGENAME}} (data page)#Structure and properties|Structure and&amp;lt;br /&amp;gt;properties]] &lt;br /&gt;
| [http://en.wikipedia.org/wiki/Refractive_index &#039;&#039;n&#039;&#039;], [http://en.wikipedia.org/wiki/Dielectric_constant ε&amp;lt;sub&amp;gt;r&amp;lt;/sub&amp;gt;], etc. &lt;br /&gt;
|-&lt;br /&gt;
| [[{{PAGENAME}} (data page)#Thermodynamic properties|Thermodynamic&amp;lt;br /&amp;gt;data]] &lt;br /&gt;
| Phase behaviour&amp;lt;br /&amp;gt;Solid, liquid, gas &lt;br /&gt;
|-&lt;br /&gt;
| [[{{PAGENAME}} (data page)#Spectral data|Spectral data]]&lt;br /&gt;
| [[UV/VIS spectroscopy|UV]], [[Infrared spectroscopy|IR]], [[nuclear magnetic resonance spectroscopy|NMR]], [[Mass spectrometry|MS]]&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Related compounds&lt;br /&gt;
|-&lt;br /&gt;
| Other [[Ion|anion]]s &amp;lt;!-- please omit if not applicable --&amp;gt;&lt;br /&gt;
| {{{Other_anion}}} &amp;lt;!-- Put in related anions e.g, iron(II) fluoride &amp;amp; iron(II) bromide if compound is iron(II) chloride --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| Other [[Ion|cation]]s &amp;lt;!-- please omit if not applicable --&amp;gt;&lt;br /&gt;
| {{{Ohter_cation}}} &amp;lt;!-- Put in other oxidation states of same element e.g. [[iron(III) chloride]], also for related metals such as [[manganese(II) chloride]], [[cobalt(II) chloride]], ruthenium(III) chloride--&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| Related compounds &lt;br /&gt;
&amp;lt;!-- A miscellaneous heading - use for covalent inorganics;  e.g. for PCl&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt; you would list PCl&amp;lt;sub&amp;gt;5&amp;lt;/sub&amp;gt;, POCl&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;, PF&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;, PBr&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;, NCl&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt; and AsCl&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;. &lt;br /&gt;
Please omit if not applicable --&amp;gt;&lt;br /&gt;
| {{{Relative_Compounds}}}&lt;br /&gt;
|-&lt;br /&gt;
| {{chembox header}} | &amp;lt;small&amp;gt;Except where noted otherwise, data are given for&amp;lt;br /&amp;gt; materials in their [[standard state|standard state (at 25&amp;amp;nbsp;°C, 100&amp;amp;nbsp;kPa)]]&amp;lt;br /&amp;gt;[[wikipedia:Chemical infobox|Infobox disclaimer and references]]&amp;lt;/small&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
|}&lt;br /&gt;
{{Chem-Data_Structure}}&lt;/div&gt;</summary>
		<author><name>Wwl06</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=Rohypnol&amp;diff=12065</id>
		<title>Rohypnol</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=Rohypnol&amp;diff=12065"/>
		<updated>2007-11-27T15:31:56Z</updated>

		<summary type="html">&lt;p&gt;Wwl06: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&amp;lt;noinclude&amp;gt;&lt;br /&gt;
&amp;lt;!-- This template has been defined after elaborate discussion in the Chemicals Wikiproject. Please do not add, deleted or otherwise change it unless after due discussion in [[wikipedia talk:WikiProject Chemicals]] --&amp;gt;&lt;br /&gt;
&amp;lt;/noinclude&amp;gt;{| class=&amp;quot;toccolours&amp;quot; border=&amp;quot;1&amp;quot; style=&amp;quot;float: right; clear: right; margin: 0 0 1em 1em; border-collapse: collapse; width: 280px&amp;quot;&lt;br /&gt;
! {{chembox header}} | {{PAGENAME}} &amp;lt;!-- replace if not identical with the article name --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image:{{PAGENAME}}.jpg|200px|{{PAGENAME}}]] &amp;lt;!-- replace if not identical with the pagename --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | General&lt;br /&gt;
|- &lt;br /&gt;
| [http://en.wikipedia.org/wiki/IUPAC Systematic name]&lt;br /&gt;
| 6-(2-fluorophenyl)-2-methyl-9-nitro-2,&lt;br /&gt;
5-diazabicyclo[5.4.0]undeca-5,8,10,12-&lt;br /&gt;
tetraen-3-one&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
| Other names&lt;br /&gt;
| {{{OtherNames}}}&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Chemical_formula Molecular formula]&lt;br /&gt;
| C16H12FN3O3&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Molar_mass Molar mass]&lt;br /&gt;
| 313.3&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
| Appearance&lt;br /&gt;
| {{{Appearance}}}&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/CAS_registry_number CAS number]&lt;br /&gt;
| {{{CASNo}}}&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Properties&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Density Density] &amp;amp; [http://en.wikipedia.org/wiki/Phase_%28matter%29 phase]&lt;br /&gt;
| {{{Density}}} g/cm³ &amp;lt;!-- ? g/cm³, solid / ? g/ml, liquid / ? g/l, gas --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Solubility Solubility in water]&lt;br /&gt;
| Almost insoluble &amp;lt;!--  at least put miscible with, not soluble in --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
&amp;lt;!-- | Other solvents e.g. [[ethanol]], [[acetone]] --&amp;gt;&lt;br /&gt;
&amp;lt;!-- | solubility info on other solvents --&amp;gt;&lt;br /&gt;
&amp;lt;!-- |- --&amp;gt;&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Melting_point Melting point]&lt;br /&gt;
| 168-172 C &amp;lt;!-- (mention any decomposition) --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Boiling_point Boiling point]&lt;br /&gt;
| {{{Bp}}} K&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Acid_dissociation_constant Acidity] (p&#039;&#039;K&#039;&#039;&amp;lt;sub&amp;gt;a&amp;lt;/sub&amp;gt;) &amp;lt;!-- omit if not an acid or a base.  If several values, be clear --&amp;gt;&lt;br /&gt;
| {{{pKa}}}&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Acid_dissociation_constant Basicity] (p&#039;&#039;K&#039;&#039;&amp;lt;sub&amp;gt;b&amp;lt;/sub&amp;gt;) &amp;lt;!-- omit if not a base. If several values, be clear --&amp;gt;&lt;br /&gt;
| {{{pKb}}}&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Specific_rotation Chiral rotation &amp;lt;nowiki&amp;gt;[α]&amp;lt;/nowiki&amp;gt;&amp;lt;sub&amp;gt;D&amp;lt;/sub&amp;gt;] &amp;lt;!-- (Only include this for chiral compounds, indicate direction/enantiomer combo if known) --&amp;gt;&lt;br /&gt;
| {{{Rotation}}}°&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Viscosity Viscosity]&lt;br /&gt;
| {{{Viscosity}}} [[Poise|cP]] at 25°C &amp;lt;!-- Liquids only, omit if data unavailable. You may use [[Pascal second|Pa.s]] if you prefer --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Structure&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Orbital_hybridisation Molecular shape] &amp;lt;!-- for simple covalent molecules (omit for most large molecules, ionics and complexes) --&amp;gt;&lt;br /&gt;
| {{{Mol_Shape}}} &amp;lt;!-- e.g. trigonal bipyramidal --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Coordination_geometry Coordination&amp;lt;br /&amp;gt;geometry] &amp;lt;!-- for a metal complex or an ionic crystal, otherwise omit --&amp;gt;&lt;br /&gt;
| {{{Coordination}}} &amp;lt;!-- e.g. trigonal bipyramidal --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Crystal_structure Crystal structure] &amp;lt;!-- omit if not a solid --&amp;gt;&lt;br /&gt;
| {{{Crystal_Structure}}} &amp;lt;!-- e.g. [[triclinic]], [[monoclinic]], [[orthorhombic]], [[hexagonal]], [[rhombohedral|trigonal]], [[tetragonal]], [[cubic]], and mention &amp;quot;close packed&amp;quot; or similar.  You may also cite what class it belongs to, e.g. [[Cadmium_chloride#Crystal_structure|CdCl&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt;]]  --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [[Dipole#Molecular_dipoles|Dipole moment]]&lt;br /&gt;
| {{{DM}}} [[Debye|D]]&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Hazards &amp;lt;!--  Summary only- MSDS entry provides more complete information --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [[Material safety data sheet|MSDS]]&lt;br /&gt;
| [[{{PAGENAME}} (data page)#Material Safety Data Sheet|External MSDS]] &amp;lt;!-- please replace with proper link--&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| Main [[Worker safety and health|hazard]]s&lt;br /&gt;
| {{{Hazards}}} &amp;lt;!-- e.g. highly toxic, explosive, flammable, corrosive --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [[NFPA 704]]&lt;br /&gt;
| {{{NFPA}}}&amp;lt;!-- {{NFPA 704 | Health=4 | Flammability=4 | Reactivity=4 | Other=OX }} These are set on &amp;quot;very dangerous&amp;quot; as default- adjust according to actual values --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [[Flash point]]&lt;br /&gt;
| {{{Fp}}}°C&lt;br /&gt;
|-&lt;br /&gt;
| [[Risk and Safety Statements|R/S statement]]&lt;br /&gt;
| [[List of R-phrases|R]]: {{{R-S}}} &amp;lt;br /&amp;gt; [[List of S-phrases|S]]: ?&lt;br /&gt;
|-&lt;br /&gt;
| [[RTECS]] number&lt;br /&gt;
| {{{RTECS}}}&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | [[{{PAGENAME}} (data page)|Supplementary data page]]&lt;br /&gt;
|-&lt;br /&gt;
| [[{{PAGENAME}} (data page)#Structure and properties|Structure and&amp;lt;br /&amp;gt;properties]] &lt;br /&gt;
| [http://en.wikipedia.org/wiki/Refractive_index &#039;&#039;n&#039;&#039;], [http://en.wikipedia.org/wiki/Dielectric_constant ε&amp;lt;sub&amp;gt;r&amp;lt;/sub&amp;gt;], etc. &lt;br /&gt;
|-&lt;br /&gt;
| [[{{PAGENAME}} (data page)#Thermodynamic properties|Thermodynamic&amp;lt;br /&amp;gt;data]] &lt;br /&gt;
| Phase behaviour&amp;lt;br /&amp;gt;Solid, liquid, gas &lt;br /&gt;
|-&lt;br /&gt;
| [[{{PAGENAME}} (data page)#Spectral data|Spectral data]]&lt;br /&gt;
| [[UV/VIS spectroscopy|UV]], [[Infrared spectroscopy|IR]], [[nuclear magnetic resonance spectroscopy|NMR]], [[Mass spectrometry|MS]]&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Related compounds&lt;br /&gt;
|-&lt;br /&gt;
| Other [[Ion|anion]]s &amp;lt;!-- please omit if not applicable --&amp;gt;&lt;br /&gt;
| {{{Other_anion}}} &amp;lt;!-- Put in related anions e.g, iron(II) fluoride &amp;amp; iron(II) bromide if compound is iron(II) chloride --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| Other [[Ion|cation]]s &amp;lt;!-- please omit if not applicable --&amp;gt;&lt;br /&gt;
| {{{Ohter_cation}}} &amp;lt;!-- Put in other oxidation states of same element e.g. [[iron(III) chloride]], also for related metals such as [[manganese(II) chloride]], [[cobalt(II) chloride]], ruthenium(III) chloride--&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| Related compounds &lt;br /&gt;
&amp;lt;!-- A miscellaneous heading - use for covalent inorganics;  e.g. for PCl&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt; you would list PCl&amp;lt;sub&amp;gt;5&amp;lt;/sub&amp;gt;, POCl&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;, PF&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;, PBr&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;, NCl&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt; and AsCl&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;. &lt;br /&gt;
Please omit if not applicable --&amp;gt;&lt;br /&gt;
| {{{Relative_Compounds}}}&lt;br /&gt;
|-&lt;br /&gt;
| {{chembox header}} | &amp;lt;small&amp;gt;Except where noted otherwise, data are given for&amp;lt;br /&amp;gt; materials in their [[standard state|standard state (at 25&amp;amp;nbsp;°C, 100&amp;amp;nbsp;kPa)]]&amp;lt;br /&amp;gt;[[wikipedia:Chemical infobox|Infobox disclaimer and references]]&amp;lt;/small&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
|}&lt;br /&gt;
{{Chem-Data_Structure}}&lt;/div&gt;</summary>
		<author><name>Wwl06</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=Rohypnol&amp;diff=12064</id>
		<title>Rohypnol</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=Rohypnol&amp;diff=12064"/>
		<updated>2007-11-27T15:30:27Z</updated>

		<summary type="html">&lt;p&gt;Wwl06: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&amp;lt;noinclude&amp;gt;&lt;br /&gt;
&amp;lt;!-- This template has been defined after elaborate discussion in the Chemicals Wikiproject. Please do not add, deleted or otherwise change it unless after due discussion in [[wikipedia talk:WikiProject Chemicals]] --&amp;gt;&lt;br /&gt;
&amp;lt;/noinclude&amp;gt;{| class=&amp;quot;toccolours&amp;quot; border=&amp;quot;1&amp;quot; style=&amp;quot;float: right; clear: right; margin: 0 0 1em 1em; border-collapse: collapse; width: 280px&amp;quot;&lt;br /&gt;
! {{chembox header}} | {{PAGENAME}} &amp;lt;!-- replace if not identical with the article name --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image:{{PAGENAME}}.jpg|200px|{{PAGENAME}}]] &amp;lt;!-- replace if not identical with the pagename --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | General&lt;br /&gt;
|- &lt;br /&gt;
| [http://en.wikipedia.org/wiki/IUPAC Systematic name]&lt;br /&gt;
| 6-(2-fluorophenyl)-2-methyl-9-nitro-2,&lt;br /&gt;
5-diazabicyclo[5.4.0]undeca-5,8,10,12-&lt;br /&gt;
tetraen-3-one&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
| Other names&lt;br /&gt;
| {{{OtherNames}}}&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Chemical_formula Molecular formula]&lt;br /&gt;
| C16H12FN3O3&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Molar_mass Molar mass]&lt;br /&gt;
| 313.3&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
| Appearance&lt;br /&gt;
| {{{Appearance}}}&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/CAS_registry_number CAS number]&lt;br /&gt;
| {{{CASNo}}}&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Properties&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Density Density] &amp;amp; [http://en.wikipedia.org/wiki/Phase_%28matter%29 phase]&lt;br /&gt;
| {{{Density}}} g/cm³ &amp;lt;!-- ? g/cm³, solid / ? g/ml, liquid / ? g/l, gas --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Solubility Solubility in water]&lt;br /&gt;
| {{{Sol_Water}}} g/100 ml (25°C) &amp;lt;!--  at least put miscible with, not soluble in --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
&amp;lt;!-- | Other solvents e.g. [[ethanol]], [[acetone]] --&amp;gt;&lt;br /&gt;
&amp;lt;!-- | solubility info on other solvents --&amp;gt;&lt;br /&gt;
&amp;lt;!-- |- --&amp;gt;&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Melting_point Melting point]&lt;br /&gt;
| 168-172 C &amp;lt;!-- (mention any decomposition) --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Boiling_point Boiling point]&lt;br /&gt;
| {{{Bp}}} K&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Acid_dissociation_constant Acidity] (p&#039;&#039;K&#039;&#039;&amp;lt;sub&amp;gt;a&amp;lt;/sub&amp;gt;) &amp;lt;!-- omit if not an acid or a base.  If several values, be clear --&amp;gt;&lt;br /&gt;
| {{{pKa}}}&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Acid_dissociation_constant Basicity] (p&#039;&#039;K&#039;&#039;&amp;lt;sub&amp;gt;b&amp;lt;/sub&amp;gt;) &amp;lt;!-- omit if not a base. If several values, be clear --&amp;gt;&lt;br /&gt;
| {{{pKb}}}&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Specific_rotation Chiral rotation &amp;lt;nowiki&amp;gt;[α]&amp;lt;/nowiki&amp;gt;&amp;lt;sub&amp;gt;D&amp;lt;/sub&amp;gt;] &amp;lt;!-- (Only include this for chiral compounds, indicate direction/enantiomer combo if known) --&amp;gt;&lt;br /&gt;
| {{{Rotation}}}°&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Viscosity Viscosity]&lt;br /&gt;
| {{{Viscosity}}} [[Poise|cP]] at 25°C &amp;lt;!-- Liquids only, omit if data unavailable. You may use [[Pascal second|Pa.s]] if you prefer --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Structure&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Orbital_hybridisation Molecular shape] &amp;lt;!-- for simple covalent molecules (omit for most large molecules, ionics and complexes) --&amp;gt;&lt;br /&gt;
| {{{Mol_Shape}}} &amp;lt;!-- e.g. trigonal bipyramidal --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Coordination_geometry Coordination&amp;lt;br /&amp;gt;geometry] &amp;lt;!-- for a metal complex or an ionic crystal, otherwise omit --&amp;gt;&lt;br /&gt;
| {{{Coordination}}} &amp;lt;!-- e.g. trigonal bipyramidal --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Crystal_structure Crystal structure] &amp;lt;!-- omit if not a solid --&amp;gt;&lt;br /&gt;
| {{{Crystal_Structure}}} &amp;lt;!-- e.g. [[triclinic]], [[monoclinic]], [[orthorhombic]], [[hexagonal]], [[rhombohedral|trigonal]], [[tetragonal]], [[cubic]], and mention &amp;quot;close packed&amp;quot; or similar.  You may also cite what class it belongs to, e.g. [[Cadmium_chloride#Crystal_structure|CdCl&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt;]]  --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [[Dipole#Molecular_dipoles|Dipole moment]]&lt;br /&gt;
| {{{DM}}} [[Debye|D]]&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Hazards &amp;lt;!--  Summary only- MSDS entry provides more complete information --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [[Material safety data sheet|MSDS]]&lt;br /&gt;
| [[{{PAGENAME}} (data page)#Material Safety Data Sheet|External MSDS]] &amp;lt;!-- please replace with proper link--&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| Main [[Worker safety and health|hazard]]s&lt;br /&gt;
| {{{Hazards}}} &amp;lt;!-- e.g. highly toxic, explosive, flammable, corrosive --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [[NFPA 704]]&lt;br /&gt;
| {{{NFPA}}}&amp;lt;!-- {{NFPA 704 | Health=4 | Flammability=4 | Reactivity=4 | Other=OX }} These are set on &amp;quot;very dangerous&amp;quot; as default- adjust according to actual values --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [[Flash point]]&lt;br /&gt;
| {{{Fp}}}°C&lt;br /&gt;
|-&lt;br /&gt;
| [[Risk and Safety Statements|R/S statement]]&lt;br /&gt;
| [[List of R-phrases|R]]: {{{R-S}}} &amp;lt;br /&amp;gt; [[List of S-phrases|S]]: ?&lt;br /&gt;
|-&lt;br /&gt;
| [[RTECS]] number&lt;br /&gt;
| {{{RTECS}}}&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | [[{{PAGENAME}} (data page)|Supplementary data page]]&lt;br /&gt;
|-&lt;br /&gt;
| [[{{PAGENAME}} (data page)#Structure and properties|Structure and&amp;lt;br /&amp;gt;properties]] &lt;br /&gt;
| [http://en.wikipedia.org/wiki/Refractive_index &#039;&#039;n&#039;&#039;], [http://en.wikipedia.org/wiki/Dielectric_constant ε&amp;lt;sub&amp;gt;r&amp;lt;/sub&amp;gt;], etc. &lt;br /&gt;
|-&lt;br /&gt;
| [[{{PAGENAME}} (data page)#Thermodynamic properties|Thermodynamic&amp;lt;br /&amp;gt;data]] &lt;br /&gt;
| Phase behaviour&amp;lt;br /&amp;gt;Solid, liquid, gas &lt;br /&gt;
|-&lt;br /&gt;
| [[{{PAGENAME}} (data page)#Spectral data|Spectral data]]&lt;br /&gt;
| [[UV/VIS spectroscopy|UV]], [[Infrared spectroscopy|IR]], [[nuclear magnetic resonance spectroscopy|NMR]], [[Mass spectrometry|MS]]&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Related compounds&lt;br /&gt;
|-&lt;br /&gt;
| Other [[Ion|anion]]s &amp;lt;!-- please omit if not applicable --&amp;gt;&lt;br /&gt;
| {{{Other_anion}}} &amp;lt;!-- Put in related anions e.g, iron(II) fluoride &amp;amp; iron(II) bromide if compound is iron(II) chloride --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| Other [[Ion|cation]]s &amp;lt;!-- please omit if not applicable --&amp;gt;&lt;br /&gt;
| {{{Ohter_cation}}} &amp;lt;!-- Put in other oxidation states of same element e.g. [[iron(III) chloride]], also for related metals such as [[manganese(II) chloride]], [[cobalt(II) chloride]], ruthenium(III) chloride--&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| Related compounds &lt;br /&gt;
&amp;lt;!-- A miscellaneous heading - use for covalent inorganics;  e.g. for PCl&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt; you would list PCl&amp;lt;sub&amp;gt;5&amp;lt;/sub&amp;gt;, POCl&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;, PF&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;, PBr&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;, NCl&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt; and AsCl&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;. &lt;br /&gt;
Please omit if not applicable --&amp;gt;&lt;br /&gt;
| {{{Relative_Compounds}}}&lt;br /&gt;
|-&lt;br /&gt;
| {{chembox header}} | &amp;lt;small&amp;gt;Except where noted otherwise, data are given for&amp;lt;br /&amp;gt; materials in their [[standard state|standard state (at 25&amp;amp;nbsp;°C, 100&amp;amp;nbsp;kPa)]]&amp;lt;br /&amp;gt;[[wikipedia:Chemical infobox|Infobox disclaimer and references]]&amp;lt;/small&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
|}&lt;br /&gt;
{{Chem-Data_Structure}}&lt;/div&gt;</summary>
		<author><name>Wwl06</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=Rohypnol&amp;diff=12060</id>
		<title>Rohypnol</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=Rohypnol&amp;diff=12060"/>
		<updated>2007-11-27T15:19:27Z</updated>

		<summary type="html">&lt;p&gt;Wwl06: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&amp;lt;noinclude&amp;gt;&lt;br /&gt;
&amp;lt;!-- This template has been defined after elaborate discussion in the Chemicals Wikiproject. Please do not add, deleted or otherwise change it unless after due discussion in [[wikipedia talk:WikiProject Chemicals]] --&amp;gt;&lt;br /&gt;
&amp;lt;/noinclude&amp;gt;{| class=&amp;quot;toccolours&amp;quot; border=&amp;quot;1&amp;quot; style=&amp;quot;float: right; clear: right; margin: 0 0 1em 1em; border-collapse: collapse; width: 280px&amp;quot;&lt;br /&gt;
! {{chembox header}} | {{PAGENAME}} &amp;lt;!-- replace if not identical with the article name --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image:{{PAGENAME}}.jpg|200px|{{PAGENAME}}]] &amp;lt;!-- replace if not identical with the pagename --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | General&lt;br /&gt;
|- &lt;br /&gt;
| [http://en.wikipedia.org/wiki/IUPAC Systematic name]&lt;br /&gt;
| 6-(2-fluorophenyl)-2-methyl-9-nitro-2,&lt;br /&gt;
5-diazabicyclo[5.4.0]undeca-5,8,10,12-&lt;br /&gt;
tetraen-3-one&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
| Other names&lt;br /&gt;
| {{{OtherNames}}}&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Chemical_formula Molecular formula]&lt;br /&gt;
| C16H12FN3O3&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Molar_mass Molar mass]&lt;br /&gt;
| 313.3&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
| Appearance&lt;br /&gt;
| {{{Appearance}}}&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/CAS_registry_number CAS number]&lt;br /&gt;
| {{{CASNo}}}&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Properties&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Density Density] &amp;amp; [http://en.wikipedia.org/wiki/Phase_%28matter%29 phase]&lt;br /&gt;
| {{{Density}}} g/cm³ &amp;lt;!-- ? g/cm³, solid / ? g/ml, liquid / ? g/l, gas --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Solubility Solubility in water]&lt;br /&gt;
| {{{Sol_Water}}} g/100 ml (25°C) &amp;lt;!--  at least put miscible with, not soluble in --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
&amp;lt;!-- | Other solvents e.g. [[ethanol]], [[acetone]] --&amp;gt;&lt;br /&gt;
&amp;lt;!-- | solubility info on other solvents --&amp;gt;&lt;br /&gt;
&amp;lt;!-- |- --&amp;gt;&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Melting_point Melting point]&lt;br /&gt;
| {{{Mp}}} K &amp;lt;!-- (mention any decomposition) --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Boiling_point Boiling point]&lt;br /&gt;
| {{{Bp}}} K&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Acid_dissociation_constant Acidity] (p&#039;&#039;K&#039;&#039;&amp;lt;sub&amp;gt;a&amp;lt;/sub&amp;gt;) &amp;lt;!-- omit if not an acid or a base.  If several values, be clear --&amp;gt;&lt;br /&gt;
| {{{pKa}}}&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Acid_dissociation_constant Basicity] (p&#039;&#039;K&#039;&#039;&amp;lt;sub&amp;gt;b&amp;lt;/sub&amp;gt;) &amp;lt;!-- omit if not a base. If several values, be clear --&amp;gt;&lt;br /&gt;
| {{{pKb}}}&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Specific_rotation Chiral rotation &amp;lt;nowiki&amp;gt;[α]&amp;lt;/nowiki&amp;gt;&amp;lt;sub&amp;gt;D&amp;lt;/sub&amp;gt;] &amp;lt;!-- (Only include this for chiral compounds, indicate direction/enantiomer combo if known) --&amp;gt;&lt;br /&gt;
| {{{Rotation}}}°&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Viscosity Viscosity]&lt;br /&gt;
| {{{Viscosity}}} [[Poise|cP]] at 25°C &amp;lt;!-- Liquids only, omit if data unavailable. You may use [[Pascal second|Pa.s]] if you prefer --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Structure&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Orbital_hybridisation Molecular shape] &amp;lt;!-- for simple covalent molecules (omit for most large molecules, ionics and complexes) --&amp;gt;&lt;br /&gt;
| {{{Mol_Shape}}} &amp;lt;!-- e.g. trigonal bipyramidal --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Coordination_geometry Coordination&amp;lt;br /&amp;gt;geometry] &amp;lt;!-- for a metal complex or an ionic crystal, otherwise omit --&amp;gt;&lt;br /&gt;
| {{{Coordination}}} &amp;lt;!-- e.g. trigonal bipyramidal --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Crystal_structure Crystal structure] &amp;lt;!-- omit if not a solid --&amp;gt;&lt;br /&gt;
| {{{Crystal_Structure}}} &amp;lt;!-- e.g. [[triclinic]], [[monoclinic]], [[orthorhombic]], [[hexagonal]], [[rhombohedral|trigonal]], [[tetragonal]], [[cubic]], and mention &amp;quot;close packed&amp;quot; or similar.  You may also cite what class it belongs to, e.g. [[Cadmium_chloride#Crystal_structure|CdCl&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt;]]  --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [[Dipole#Molecular_dipoles|Dipole moment]]&lt;br /&gt;
| {{{DM}}} [[Debye|D]]&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Hazards &amp;lt;!--  Summary only- MSDS entry provides more complete information --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [[Material safety data sheet|MSDS]]&lt;br /&gt;
| [[{{PAGENAME}} (data page)#Material Safety Data Sheet|External MSDS]] &amp;lt;!-- please replace with proper link--&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| Main [[Worker safety and health|hazard]]s&lt;br /&gt;
| {{{Hazards}}} &amp;lt;!-- e.g. highly toxic, explosive, flammable, corrosive --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [[NFPA 704]]&lt;br /&gt;
| {{{NFPA}}}&amp;lt;!-- {{NFPA 704 | Health=4 | Flammability=4 | Reactivity=4 | Other=OX }} These are set on &amp;quot;very dangerous&amp;quot; as default- adjust according to actual values --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [[Flash point]]&lt;br /&gt;
| {{{Fp}}}°C&lt;br /&gt;
|-&lt;br /&gt;
| [[Risk and Safety Statements|R/S statement]]&lt;br /&gt;
| [[List of R-phrases|R]]: {{{R-S}}} &amp;lt;br /&amp;gt; [[List of S-phrases|S]]: ?&lt;br /&gt;
|-&lt;br /&gt;
| [[RTECS]] number&lt;br /&gt;
| {{{RTECS}}}&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | [[{{PAGENAME}} (data page)|Supplementary data page]]&lt;br /&gt;
|-&lt;br /&gt;
| [[{{PAGENAME}} (data page)#Structure and properties|Structure and&amp;lt;br /&amp;gt;properties]] &lt;br /&gt;
| [http://en.wikipedia.org/wiki/Refractive_index &#039;&#039;n&#039;&#039;], [http://en.wikipedia.org/wiki/Dielectric_constant ε&amp;lt;sub&amp;gt;r&amp;lt;/sub&amp;gt;], etc. &lt;br /&gt;
|-&lt;br /&gt;
| [[{{PAGENAME}} (data page)#Thermodynamic properties|Thermodynamic&amp;lt;br /&amp;gt;data]] &lt;br /&gt;
| Phase behaviour&amp;lt;br /&amp;gt;Solid, liquid, gas &lt;br /&gt;
|-&lt;br /&gt;
| [[{{PAGENAME}} (data page)#Spectral data|Spectral data]]&lt;br /&gt;
| [[UV/VIS spectroscopy|UV]], [[Infrared spectroscopy|IR]], [[nuclear magnetic resonance spectroscopy|NMR]], [[Mass spectrometry|MS]]&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Related compounds&lt;br /&gt;
|-&lt;br /&gt;
| Other [[Ion|anion]]s &amp;lt;!-- please omit if not applicable --&amp;gt;&lt;br /&gt;
| {{{Other_anion}}} &amp;lt;!-- Put in related anions e.g, iron(II) fluoride &amp;amp; iron(II) bromide if compound is iron(II) chloride --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| Other [[Ion|cation]]s &amp;lt;!-- please omit if not applicable --&amp;gt;&lt;br /&gt;
| {{{Ohter_cation}}} &amp;lt;!-- Put in other oxidation states of same element e.g. [[iron(III) chloride]], also for related metals such as [[manganese(II) chloride]], [[cobalt(II) chloride]], ruthenium(III) chloride--&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| Related compounds &lt;br /&gt;
&amp;lt;!-- A miscellaneous heading - use for covalent inorganics;  e.g. for PCl&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt; you would list PCl&amp;lt;sub&amp;gt;5&amp;lt;/sub&amp;gt;, POCl&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;, PF&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;, PBr&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;, NCl&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt; and AsCl&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;. &lt;br /&gt;
Please omit if not applicable --&amp;gt;&lt;br /&gt;
| {{{Relative_Compounds}}}&lt;br /&gt;
|-&lt;br /&gt;
| {{chembox header}} | &amp;lt;small&amp;gt;Except where noted otherwise, data are given for&amp;lt;br /&amp;gt; materials in their [[standard state|standard state (at 25&amp;amp;nbsp;°C, 100&amp;amp;nbsp;kPa)]]&amp;lt;br /&amp;gt;[[wikipedia:Chemical infobox|Infobox disclaimer and references]]&amp;lt;/small&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
|}&lt;br /&gt;
{{Chem-Data_Structure}}&lt;/div&gt;</summary>
		<author><name>Wwl06</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=Rohypnol&amp;diff=12059</id>
		<title>Rohypnol</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=Rohypnol&amp;diff=12059"/>
		<updated>2007-11-27T15:19:12Z</updated>

		<summary type="html">&lt;p&gt;Wwl06: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&amp;lt;noinclude&amp;gt;&lt;br /&gt;
&amp;lt;!-- This template has been defined after elaborate discussion in the Chemicals Wikiproject. Please do not add, deleted or otherwise change it unless after due discussion in [[wikipedia talk:WikiProject Chemicals]] --&amp;gt;&lt;br /&gt;
&amp;lt;/noinclude&amp;gt;{| class=&amp;quot;toccolours&amp;quot; border=&amp;quot;1&amp;quot; style=&amp;quot;float: right; clear: right; margin: 0 0 1em 1em; border-collapse: collapse; width: 280px&amp;quot;&lt;br /&gt;
! {{chembox header}} | {{PAGENAME}} &amp;lt;!-- replace if not identical with the article name --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image:{{PAGENAME}}.jpg|200px|{{PAGENAME}}]] &amp;lt;!-- replace if not identical with the pagename --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | General&lt;br /&gt;
|- &lt;br /&gt;
| [http://en.wikipedia.org/wiki/IUPAC Systematic name]&lt;br /&gt;
| 6-(2-fluorophenyl)-2-methyl-9-nitro-2,&lt;br /&gt;
5-diazabicyclo[5.4.0]undeca-5,8,10,12-&lt;br /&gt;
tetraen-3-one&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
| Other names&lt;br /&gt;
| {{{OtherNames}}}&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Chemical_formula Molecular formula]&lt;br /&gt;
| {{{C16H12FN3O3}}} &lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Molar_mass Molar mass]&lt;br /&gt;
| {{{313.3}}}&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
| Appearance&lt;br /&gt;
| {{{Appearance}}}&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/CAS_registry_number CAS number]&lt;br /&gt;
| {{{CASNo}}}&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Properties&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Density Density] &amp;amp; [http://en.wikipedia.org/wiki/Phase_%28matter%29 phase]&lt;br /&gt;
| {{{Density}}} g/cm³ &amp;lt;!-- ? g/cm³, solid / ? g/ml, liquid / ? g/l, gas --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Solubility Solubility in water]&lt;br /&gt;
| {{{Sol_Water}}} g/100 ml (25°C) &amp;lt;!--  at least put miscible with, not soluble in --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
&amp;lt;!-- | Other solvents e.g. [[ethanol]], [[acetone]] --&amp;gt;&lt;br /&gt;
&amp;lt;!-- | solubility info on other solvents --&amp;gt;&lt;br /&gt;
&amp;lt;!-- |- --&amp;gt;&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Melting_point Melting point]&lt;br /&gt;
| {{{Mp}}} K &amp;lt;!-- (mention any decomposition) --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Boiling_point Boiling point]&lt;br /&gt;
| {{{Bp}}} K&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Acid_dissociation_constant Acidity] (p&#039;&#039;K&#039;&#039;&amp;lt;sub&amp;gt;a&amp;lt;/sub&amp;gt;) &amp;lt;!-- omit if not an acid or a base.  If several values, be clear --&amp;gt;&lt;br /&gt;
| {{{pKa}}}&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Acid_dissociation_constant Basicity] (p&#039;&#039;K&#039;&#039;&amp;lt;sub&amp;gt;b&amp;lt;/sub&amp;gt;) &amp;lt;!-- omit if not a base. If several values, be clear --&amp;gt;&lt;br /&gt;
| {{{pKb}}}&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Specific_rotation Chiral rotation &amp;lt;nowiki&amp;gt;[α]&amp;lt;/nowiki&amp;gt;&amp;lt;sub&amp;gt;D&amp;lt;/sub&amp;gt;] &amp;lt;!-- (Only include this for chiral compounds, indicate direction/enantiomer combo if known) --&amp;gt;&lt;br /&gt;
| {{{Rotation}}}°&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Viscosity Viscosity]&lt;br /&gt;
| {{{Viscosity}}} [[Poise|cP]] at 25°C &amp;lt;!-- Liquids only, omit if data unavailable. You may use [[Pascal second|Pa.s]] if you prefer --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Structure&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Orbital_hybridisation Molecular shape] &amp;lt;!-- for simple covalent molecules (omit for most large molecules, ionics and complexes) --&amp;gt;&lt;br /&gt;
| {{{Mol_Shape}}} &amp;lt;!-- e.g. trigonal bipyramidal --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Coordination_geometry Coordination&amp;lt;br /&amp;gt;geometry] &amp;lt;!-- for a metal complex or an ionic crystal, otherwise omit --&amp;gt;&lt;br /&gt;
| {{{Coordination}}} &amp;lt;!-- e.g. trigonal bipyramidal --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Crystal_structure Crystal structure] &amp;lt;!-- omit if not a solid --&amp;gt;&lt;br /&gt;
| {{{Crystal_Structure}}} &amp;lt;!-- e.g. [[triclinic]], [[monoclinic]], [[orthorhombic]], [[hexagonal]], [[rhombohedral|trigonal]], [[tetragonal]], [[cubic]], and mention &amp;quot;close packed&amp;quot; or similar.  You may also cite what class it belongs to, e.g. [[Cadmium_chloride#Crystal_structure|CdCl&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt;]]  --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [[Dipole#Molecular_dipoles|Dipole moment]]&lt;br /&gt;
| {{{DM}}} [[Debye|D]]&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Hazards &amp;lt;!--  Summary only- MSDS entry provides more complete information --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [[Material safety data sheet|MSDS]]&lt;br /&gt;
| [[{{PAGENAME}} (data page)#Material Safety Data Sheet|External MSDS]] &amp;lt;!-- please replace with proper link--&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| Main [[Worker safety and health|hazard]]s&lt;br /&gt;
| {{{Hazards}}} &amp;lt;!-- e.g. highly toxic, explosive, flammable, corrosive --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [[NFPA 704]]&lt;br /&gt;
| {{{NFPA}}}&amp;lt;!-- {{NFPA 704 | Health=4 | Flammability=4 | Reactivity=4 | Other=OX }} These are set on &amp;quot;very dangerous&amp;quot; as default- adjust according to actual values --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [[Flash point]]&lt;br /&gt;
| {{{Fp}}}°C&lt;br /&gt;
|-&lt;br /&gt;
| [[Risk and Safety Statements|R/S statement]]&lt;br /&gt;
| [[List of R-phrases|R]]: {{{R-S}}} &amp;lt;br /&amp;gt; [[List of S-phrases|S]]: ?&lt;br /&gt;
|-&lt;br /&gt;
| [[RTECS]] number&lt;br /&gt;
| {{{RTECS}}}&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | [[{{PAGENAME}} (data page)|Supplementary data page]]&lt;br /&gt;
|-&lt;br /&gt;
| [[{{PAGENAME}} (data page)#Structure and properties|Structure and&amp;lt;br /&amp;gt;properties]] &lt;br /&gt;
| [http://en.wikipedia.org/wiki/Refractive_index &#039;&#039;n&#039;&#039;], [http://en.wikipedia.org/wiki/Dielectric_constant ε&amp;lt;sub&amp;gt;r&amp;lt;/sub&amp;gt;], etc. &lt;br /&gt;
|-&lt;br /&gt;
| [[{{PAGENAME}} (data page)#Thermodynamic properties|Thermodynamic&amp;lt;br /&amp;gt;data]] &lt;br /&gt;
| Phase behaviour&amp;lt;br /&amp;gt;Solid, liquid, gas &lt;br /&gt;
|-&lt;br /&gt;
| [[{{PAGENAME}} (data page)#Spectral data|Spectral data]]&lt;br /&gt;
| [[UV/VIS spectroscopy|UV]], [[Infrared spectroscopy|IR]], [[nuclear magnetic resonance spectroscopy|NMR]], [[Mass spectrometry|MS]]&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Related compounds&lt;br /&gt;
|-&lt;br /&gt;
| Other [[Ion|anion]]s &amp;lt;!-- please omit if not applicable --&amp;gt;&lt;br /&gt;
| {{{Other_anion}}} &amp;lt;!-- Put in related anions e.g, iron(II) fluoride &amp;amp; iron(II) bromide if compound is iron(II) chloride --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| Other [[Ion|cation]]s &amp;lt;!-- please omit if not applicable --&amp;gt;&lt;br /&gt;
| {{{Ohter_cation}}} &amp;lt;!-- Put in other oxidation states of same element e.g. [[iron(III) chloride]], also for related metals such as [[manganese(II) chloride]], [[cobalt(II) chloride]], ruthenium(III) chloride--&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| Related compounds &lt;br /&gt;
&amp;lt;!-- A miscellaneous heading - use for covalent inorganics;  e.g. for PCl&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt; you would list PCl&amp;lt;sub&amp;gt;5&amp;lt;/sub&amp;gt;, POCl&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;, PF&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;, PBr&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;, NCl&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt; and AsCl&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;. &lt;br /&gt;
Please omit if not applicable --&amp;gt;&lt;br /&gt;
| {{{Relative_Compounds}}}&lt;br /&gt;
|-&lt;br /&gt;
| {{chembox header}} | &amp;lt;small&amp;gt;Except where noted otherwise, data are given for&amp;lt;br /&amp;gt; materials in their [[standard state|standard state (at 25&amp;amp;nbsp;°C, 100&amp;amp;nbsp;kPa)]]&amp;lt;br /&amp;gt;[[wikipedia:Chemical infobox|Infobox disclaimer and references]]&amp;lt;/small&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
|}&lt;br /&gt;
{{Chem-Data_Structure}}&lt;/div&gt;</summary>
		<author><name>Wwl06</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=Rohypnol&amp;diff=12058</id>
		<title>Rohypnol</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=Rohypnol&amp;diff=12058"/>
		<updated>2007-11-27T15:18:49Z</updated>

		<summary type="html">&lt;p&gt;Wwl06: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&amp;lt;noinclude&amp;gt;&lt;br /&gt;
&amp;lt;!-- This template has been defined after elaborate discussion in the Chemicals Wikiproject. Please do not add, deleted or otherwise change it unless after due discussion in [[wikipedia talk:WikiProject Chemicals]] --&amp;gt;&lt;br /&gt;
&amp;lt;/noinclude&amp;gt;{| class=&amp;quot;toccolours&amp;quot; border=&amp;quot;1&amp;quot; style=&amp;quot;float: right; clear: right; margin: 0 0 1em 1em; border-collapse: collapse; width: 280px&amp;quot;&lt;br /&gt;
! {{chembox header}} | {{PAGENAME}} &amp;lt;!-- replace if not identical with the article name --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image:{{PAGENAME}}.jpg|200px|{{PAGENAME}}]] &amp;lt;!-- replace if not identical with the pagename --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | General&lt;br /&gt;
|- &lt;br /&gt;
| [http://en.wikipedia.org/wiki/IUPAC Systematic name]&lt;br /&gt;
| {{{6-(2-fluorophenyl)-2-methyl-9-nitro-2,&lt;br /&gt;
5-diazabicyclo[5.4.0]undeca-5,8,10,12-&lt;br /&gt;
tetraen-3-one}}}&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
| Other names&lt;br /&gt;
| {{{OtherNames}}}&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Chemical_formula Molecular formula]&lt;br /&gt;
| {{{C16H12FN3O3}}} &lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Molar_mass Molar mass]&lt;br /&gt;
| {{{313.3}}}&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
| Appearance&lt;br /&gt;
| {{{Appearance}}}&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/CAS_registry_number CAS number]&lt;br /&gt;
| {{{CASNo}}}&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Properties&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Density Density] &amp;amp; [http://en.wikipedia.org/wiki/Phase_%28matter%29 phase]&lt;br /&gt;
| {{{Density}}} g/cm³ &amp;lt;!-- ? g/cm³, solid / ? g/ml, liquid / ? g/l, gas --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Solubility Solubility in water]&lt;br /&gt;
| {{{Sol_Water}}} g/100 ml (25°C) &amp;lt;!--  at least put miscible with, not soluble in --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
&amp;lt;!-- | Other solvents e.g. [[ethanol]], [[acetone]] --&amp;gt;&lt;br /&gt;
&amp;lt;!-- | solubility info on other solvents --&amp;gt;&lt;br /&gt;
&amp;lt;!-- |- --&amp;gt;&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Melting_point Melting point]&lt;br /&gt;
| {{{Mp}}} K &amp;lt;!-- (mention any decomposition) --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Boiling_point Boiling point]&lt;br /&gt;
| {{{Bp}}} K&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Acid_dissociation_constant Acidity] (p&#039;&#039;K&#039;&#039;&amp;lt;sub&amp;gt;a&amp;lt;/sub&amp;gt;) &amp;lt;!-- omit if not an acid or a base.  If several values, be clear --&amp;gt;&lt;br /&gt;
| {{{pKa}}}&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Acid_dissociation_constant Basicity] (p&#039;&#039;K&#039;&#039;&amp;lt;sub&amp;gt;b&amp;lt;/sub&amp;gt;) &amp;lt;!-- omit if not a base. If several values, be clear --&amp;gt;&lt;br /&gt;
| {{{pKb}}}&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Specific_rotation Chiral rotation &amp;lt;nowiki&amp;gt;[α]&amp;lt;/nowiki&amp;gt;&amp;lt;sub&amp;gt;D&amp;lt;/sub&amp;gt;] &amp;lt;!-- (Only include this for chiral compounds, indicate direction/enantiomer combo if known) --&amp;gt;&lt;br /&gt;
| {{{Rotation}}}°&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Viscosity Viscosity]&lt;br /&gt;
| {{{Viscosity}}} [[Poise|cP]] at 25°C &amp;lt;!-- Liquids only, omit if data unavailable. You may use [[Pascal second|Pa.s]] if you prefer --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Structure&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Orbital_hybridisation Molecular shape] &amp;lt;!-- for simple covalent molecules (omit for most large molecules, ionics and complexes) --&amp;gt;&lt;br /&gt;
| {{{Mol_Shape}}} &amp;lt;!-- e.g. trigonal bipyramidal --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Coordination_geometry Coordination&amp;lt;br /&amp;gt;geometry] &amp;lt;!-- for a metal complex or an ionic crystal, otherwise omit --&amp;gt;&lt;br /&gt;
| {{{Coordination}}} &amp;lt;!-- e.g. trigonal bipyramidal --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Crystal_structure Crystal structure] &amp;lt;!-- omit if not a solid --&amp;gt;&lt;br /&gt;
| {{{Crystal_Structure}}} &amp;lt;!-- e.g. [[triclinic]], [[monoclinic]], [[orthorhombic]], [[hexagonal]], [[rhombohedral|trigonal]], [[tetragonal]], [[cubic]], and mention &amp;quot;close packed&amp;quot; or similar.  You may also cite what class it belongs to, e.g. [[Cadmium_chloride#Crystal_structure|CdCl&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt;]]  --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [[Dipole#Molecular_dipoles|Dipole moment]]&lt;br /&gt;
| {{{DM}}} [[Debye|D]]&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Hazards &amp;lt;!--  Summary only- MSDS entry provides more complete information --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [[Material safety data sheet|MSDS]]&lt;br /&gt;
| [[{{PAGENAME}} (data page)#Material Safety Data Sheet|External MSDS]] &amp;lt;!-- please replace with proper link--&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| Main [[Worker safety and health|hazard]]s&lt;br /&gt;
| {{{Hazards}}} &amp;lt;!-- e.g. highly toxic, explosive, flammable, corrosive --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [[NFPA 704]]&lt;br /&gt;
| {{{NFPA}}}&amp;lt;!-- {{NFPA 704 | Health=4 | Flammability=4 | Reactivity=4 | Other=OX }} These are set on &amp;quot;very dangerous&amp;quot; as default- adjust according to actual values --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [[Flash point]]&lt;br /&gt;
| {{{Fp}}}°C&lt;br /&gt;
|-&lt;br /&gt;
| [[Risk and Safety Statements|R/S statement]]&lt;br /&gt;
| [[List of R-phrases|R]]: {{{R-S}}} &amp;lt;br /&amp;gt; [[List of S-phrases|S]]: ?&lt;br /&gt;
|-&lt;br /&gt;
| [[RTECS]] number&lt;br /&gt;
| {{{RTECS}}}&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | [[{{PAGENAME}} (data page)|Supplementary data page]]&lt;br /&gt;
|-&lt;br /&gt;
| [[{{PAGENAME}} (data page)#Structure and properties|Structure and&amp;lt;br /&amp;gt;properties]] &lt;br /&gt;
| [http://en.wikipedia.org/wiki/Refractive_index &#039;&#039;n&#039;&#039;], [http://en.wikipedia.org/wiki/Dielectric_constant ε&amp;lt;sub&amp;gt;r&amp;lt;/sub&amp;gt;], etc. &lt;br /&gt;
|-&lt;br /&gt;
| [[{{PAGENAME}} (data page)#Thermodynamic properties|Thermodynamic&amp;lt;br /&amp;gt;data]] &lt;br /&gt;
| Phase behaviour&amp;lt;br /&amp;gt;Solid, liquid, gas &lt;br /&gt;
|-&lt;br /&gt;
| [[{{PAGENAME}} (data page)#Spectral data|Spectral data]]&lt;br /&gt;
| [[UV/VIS spectroscopy|UV]], [[Infrared spectroscopy|IR]], [[nuclear magnetic resonance spectroscopy|NMR]], [[Mass spectrometry|MS]]&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Related compounds&lt;br /&gt;
|-&lt;br /&gt;
| Other [[Ion|anion]]s &amp;lt;!-- please omit if not applicable --&amp;gt;&lt;br /&gt;
| {{{Other_anion}}} &amp;lt;!-- Put in related anions e.g, iron(II) fluoride &amp;amp; iron(II) bromide if compound is iron(II) chloride --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| Other [[Ion|cation]]s &amp;lt;!-- please omit if not applicable --&amp;gt;&lt;br /&gt;
| {{{Ohter_cation}}} &amp;lt;!-- Put in other oxidation states of same element e.g. [[iron(III) chloride]], also for related metals such as [[manganese(II) chloride]], [[cobalt(II) chloride]], ruthenium(III) chloride--&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| Related compounds &lt;br /&gt;
&amp;lt;!-- A miscellaneous heading - use for covalent inorganics;  e.g. for PCl&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt; you would list PCl&amp;lt;sub&amp;gt;5&amp;lt;/sub&amp;gt;, POCl&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;, PF&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;, PBr&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;, NCl&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt; and AsCl&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;. &lt;br /&gt;
Please omit if not applicable --&amp;gt;&lt;br /&gt;
| {{{Relative_Compounds}}}&lt;br /&gt;
|-&lt;br /&gt;
| {{chembox header}} | &amp;lt;small&amp;gt;Except where noted otherwise, data are given for&amp;lt;br /&amp;gt; materials in their [[standard state|standard state (at 25&amp;amp;nbsp;°C, 100&amp;amp;nbsp;kPa)]]&amp;lt;br /&amp;gt;[[wikipedia:Chemical infobox|Infobox disclaimer and references]]&amp;lt;/small&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
|}&lt;br /&gt;
{{Chem-Data_Structure}}&lt;/div&gt;</summary>
		<author><name>Wwl06</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=Rohypnol&amp;diff=12056</id>
		<title>Rohypnol</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=Rohypnol&amp;diff=12056"/>
		<updated>2007-11-27T15:17:30Z</updated>

		<summary type="html">&lt;p&gt;Wwl06: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&amp;lt;noinclude&amp;gt;&lt;br /&gt;
&amp;lt;!-- This template has been defined after elaborate discussion in the Chemicals Wikiproject. Please do not add, deleted or otherwise change it unless after due discussion in [[wikipedia talk:WikiProject Chemicals]] --&amp;gt;&lt;br /&gt;
&amp;lt;/noinclude&amp;gt;{| class=&amp;quot;toccolours&amp;quot; border=&amp;quot;1&amp;quot; style=&amp;quot;float: right; clear: right; margin: 0 0 1em 1em; border-collapse: collapse; width: 280px&amp;quot;&lt;br /&gt;
! {{chembox header}} | {{PAGENAME}} &amp;lt;!-- replace if not identical with the article name --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image:{{PAGENAME}}.jpg|200px|{{PAGENAME}}]] &amp;lt;!-- replace if not identical with the pagename --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | General&lt;br /&gt;
|- &lt;br /&gt;
| [http://en.wikipedia.org/wiki/IUPAC Systematic name]&lt;br /&gt;
| {{{6-(2-fluorophenyl)-2-methyl-9-nitro-2,&lt;br /&gt;
5-diazabicyclo[5.4.0]undeca-5,8,10,12-&lt;br /&gt;
tetraen-3-one}}}&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
| Other names&lt;br /&gt;
| {{{OtherNames}}}&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Chemical_formula Molecular formula]&lt;br /&gt;
| {{{Formula}}} &lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Chemical_file_format SMILES] &amp;lt;!-- mostly for organic compounds, omit otherwise --&amp;gt;&lt;br /&gt;
| {{{SMILES}}}&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Molar_mass Molar mass]&lt;br /&gt;
| {{{MolarMass}}}&lt;br /&gt;
|-&lt;br /&gt;
| Appearance&lt;br /&gt;
| {{{Appearance}}}&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/CAS_registry_number CAS number]&lt;br /&gt;
| {{{CASNo}}}&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Properties&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Density Density] &amp;amp; [http://en.wikipedia.org/wiki/Phase_%28matter%29 phase]&lt;br /&gt;
| {{{Density}}} g/cm³ &amp;lt;!-- ? g/cm³, solid / ? g/ml, liquid / ? g/l, gas --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Solubility Solubility in water]&lt;br /&gt;
| {{{Sol_Water}}} g/100 ml (25°C) &amp;lt;!--  at least put miscible with, not soluble in --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
&amp;lt;!-- | Other solvents e.g. [[ethanol]], [[acetone]] --&amp;gt;&lt;br /&gt;
&amp;lt;!-- | solubility info on other solvents --&amp;gt;&lt;br /&gt;
&amp;lt;!-- |- --&amp;gt;&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Melting_point Melting point]&lt;br /&gt;
| {{{Mp}}} K &amp;lt;!-- (mention any decomposition) --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Boiling_point Boiling point]&lt;br /&gt;
| {{{Bp}}} K&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Acid_dissociation_constant Acidity] (p&#039;&#039;K&#039;&#039;&amp;lt;sub&amp;gt;a&amp;lt;/sub&amp;gt;) &amp;lt;!-- omit if not an acid or a base.  If several values, be clear --&amp;gt;&lt;br /&gt;
| {{{pKa}}}&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Acid_dissociation_constant Basicity] (p&#039;&#039;K&#039;&#039;&amp;lt;sub&amp;gt;b&amp;lt;/sub&amp;gt;) &amp;lt;!-- omit if not a base. If several values, be clear --&amp;gt;&lt;br /&gt;
| {{{pKb}}}&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Specific_rotation Chiral rotation &amp;lt;nowiki&amp;gt;[α]&amp;lt;/nowiki&amp;gt;&amp;lt;sub&amp;gt;D&amp;lt;/sub&amp;gt;] &amp;lt;!-- (Only include this for chiral compounds, indicate direction/enantiomer combo if known) --&amp;gt;&lt;br /&gt;
| {{{Rotation}}}°&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Viscosity Viscosity]&lt;br /&gt;
| {{{Viscosity}}} [[Poise|cP]] at 25°C &amp;lt;!-- Liquids only, omit if data unavailable. You may use [[Pascal second|Pa.s]] if you prefer --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Structure&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Orbital_hybridisation Molecular shape] &amp;lt;!-- for simple covalent molecules (omit for most large molecules, ionics and complexes) --&amp;gt;&lt;br /&gt;
| {{{Mol_Shape}}} &amp;lt;!-- e.g. trigonal bipyramidal --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Coordination_geometry Coordination&amp;lt;br /&amp;gt;geometry] &amp;lt;!-- for a metal complex or an ionic crystal, otherwise omit --&amp;gt;&lt;br /&gt;
| {{{Coordination}}} &amp;lt;!-- e.g. trigonal bipyramidal --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Crystal_structure Crystal structure] &amp;lt;!-- omit if not a solid --&amp;gt;&lt;br /&gt;
| {{{Crystal_Structure}}} &amp;lt;!-- e.g. [[triclinic]], [[monoclinic]], [[orthorhombic]], [[hexagonal]], [[rhombohedral|trigonal]], [[tetragonal]], [[cubic]], and mention &amp;quot;close packed&amp;quot; or similar.  You may also cite what class it belongs to, e.g. [[Cadmium_chloride#Crystal_structure|CdCl&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt;]]  --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [[Dipole#Molecular_dipoles|Dipole moment]]&lt;br /&gt;
| {{{DM}}} [[Debye|D]]&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Hazards &amp;lt;!--  Summary only- MSDS entry provides more complete information --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [[Material safety data sheet|MSDS]]&lt;br /&gt;
| [[{{PAGENAME}} (data page)#Material Safety Data Sheet|External MSDS]] &amp;lt;!-- please replace with proper link--&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| Main [[Worker safety and health|hazard]]s&lt;br /&gt;
| {{{Hazards}}} &amp;lt;!-- e.g. highly toxic, explosive, flammable, corrosive --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [[NFPA 704]]&lt;br /&gt;
| {{{NFPA}}}&amp;lt;!-- {{NFPA 704 | Health=4 | Flammability=4 | Reactivity=4 | Other=OX }} These are set on &amp;quot;very dangerous&amp;quot; as default- adjust according to actual values --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [[Flash point]]&lt;br /&gt;
| {{{Fp}}}°C&lt;br /&gt;
|-&lt;br /&gt;
| [[Risk and Safety Statements|R/S statement]]&lt;br /&gt;
| [[List of R-phrases|R]]: {{{R-S}}} &amp;lt;br /&amp;gt; [[List of S-phrases|S]]: ?&lt;br /&gt;
|-&lt;br /&gt;
| [[RTECS]] number&lt;br /&gt;
| {{{RTECS}}}&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | [[{{PAGENAME}} (data page)|Supplementary data page]]&lt;br /&gt;
|-&lt;br /&gt;
| [[{{PAGENAME}} (data page)#Structure and properties|Structure and&amp;lt;br /&amp;gt;properties]] &lt;br /&gt;
| [http://en.wikipedia.org/wiki/Refractive_index &#039;&#039;n&#039;&#039;], [http://en.wikipedia.org/wiki/Dielectric_constant ε&amp;lt;sub&amp;gt;r&amp;lt;/sub&amp;gt;], etc. &lt;br /&gt;
|-&lt;br /&gt;
| [[{{PAGENAME}} (data page)#Thermodynamic properties|Thermodynamic&amp;lt;br /&amp;gt;data]] &lt;br /&gt;
| Phase behaviour&amp;lt;br /&amp;gt;Solid, liquid, gas &lt;br /&gt;
|-&lt;br /&gt;
| [[{{PAGENAME}} (data page)#Spectral data|Spectral data]]&lt;br /&gt;
| [[UV/VIS spectroscopy|UV]], [[Infrared spectroscopy|IR]], [[nuclear magnetic resonance spectroscopy|NMR]], [[Mass spectrometry|MS]]&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Related compounds&lt;br /&gt;
|-&lt;br /&gt;
| Other [[Ion|anion]]s &amp;lt;!-- please omit if not applicable --&amp;gt;&lt;br /&gt;
| {{{Other_anion}}} &amp;lt;!-- Put in related anions e.g, iron(II) fluoride &amp;amp; iron(II) bromide if compound is iron(II) chloride --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| Other [[Ion|cation]]s &amp;lt;!-- please omit if not applicable --&amp;gt;&lt;br /&gt;
| {{{Ohter_cation}}} &amp;lt;!-- Put in other oxidation states of same element e.g. [[iron(III) chloride]], also for related metals such as [[manganese(II) chloride]], [[cobalt(II) chloride]], ruthenium(III) chloride--&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| Related compounds &lt;br /&gt;
&amp;lt;!-- A miscellaneous heading - use for covalent inorganics;  e.g. for PCl&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt; you would list PCl&amp;lt;sub&amp;gt;5&amp;lt;/sub&amp;gt;, POCl&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;, PF&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;, PBr&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;, NCl&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt; and AsCl&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;. &lt;br /&gt;
Please omit if not applicable --&amp;gt;&lt;br /&gt;
| {{{Relative_Compounds}}}&lt;br /&gt;
|-&lt;br /&gt;
| {{chembox header}} | &amp;lt;small&amp;gt;Except where noted otherwise, data are given for&amp;lt;br /&amp;gt; materials in their [[standard state|standard state (at 25&amp;amp;nbsp;°C, 100&amp;amp;nbsp;kPa)]]&amp;lt;br /&amp;gt;[[wikipedia:Chemical infobox|Infobox disclaimer and references]]&amp;lt;/small&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
|}&lt;br /&gt;
{{Chem-Data_Structure}}&lt;/div&gt;</summary>
		<author><name>Wwl06</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=Rohypnol&amp;diff=12054</id>
		<title>Rohypnol</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=Rohypnol&amp;diff=12054"/>
		<updated>2007-11-27T15:16:59Z</updated>

		<summary type="html">&lt;p&gt;Wwl06: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&amp;lt;noinclude&amp;gt;&lt;br /&gt;
&amp;lt;!-- This template has been defined after elaborate discussion in the Chemicals Wikiproject. Please do not add, deleted or otherwise change it unless after due discussion in [[wikipedia talk:WikiProject Chemicals]] --&amp;gt;&lt;br /&gt;
&amp;lt;/noinclude&amp;gt;{| class=&amp;quot;toccolours&amp;quot; border=&amp;quot;1&amp;quot; style=&amp;quot;float: right; clear: right; margin: 0 0 1em 1em; border-collapse: collapse; width: 280px&amp;quot;&lt;br /&gt;
! {{chembox header}} | {{PAGENAME}} &amp;lt;!-- replace if not identical with the article name --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image:{{PAGENAME}}.jpg|200px|{{PAGENAME}}]] &amp;lt;!-- replace if not identical with the pagename --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | General&lt;br /&gt;
|- &lt;br /&gt;
| [http://en.wikipedia.org/wiki/IUPAC Systematic name]&lt;br /&gt;
| {{{6-(2-fluorophenyl)-2-methyl-9-nitro-2,5-diazabicyclo[5.4.0]undeca-5,8,10,12-tetraen-3-one}}}&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
| Other names&lt;br /&gt;
| {{{OtherNames}}}&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Chemical_formula Molecular formula]&lt;br /&gt;
| {{{Formula}}} &lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Chemical_file_format SMILES] &amp;lt;!-- mostly for organic compounds, omit otherwise --&amp;gt;&lt;br /&gt;
| {{{SMILES}}}&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Molar_mass Molar mass]&lt;br /&gt;
| {{{MolarMass}}}&lt;br /&gt;
|-&lt;br /&gt;
| Appearance&lt;br /&gt;
| {{{Appearance}}}&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/CAS_registry_number CAS number]&lt;br /&gt;
| {{{CASNo}}}&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Properties&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Density Density] &amp;amp; [http://en.wikipedia.org/wiki/Phase_%28matter%29 phase]&lt;br /&gt;
| {{{Density}}} g/cm³ &amp;lt;!-- ? g/cm³, solid / ? g/ml, liquid / ? g/l, gas --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Solubility Solubility in water]&lt;br /&gt;
| {{{Sol_Water}}} g/100 ml (25°C) &amp;lt;!--  at least put miscible with, not soluble in --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
&amp;lt;!-- | Other solvents e.g. [[ethanol]], [[acetone]] --&amp;gt;&lt;br /&gt;
&amp;lt;!-- | solubility info on other solvents --&amp;gt;&lt;br /&gt;
&amp;lt;!-- |- --&amp;gt;&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Melting_point Melting point]&lt;br /&gt;
| {{{Mp}}} K &amp;lt;!-- (mention any decomposition) --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Boiling_point Boiling point]&lt;br /&gt;
| {{{Bp}}} K&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Acid_dissociation_constant Acidity] (p&#039;&#039;K&#039;&#039;&amp;lt;sub&amp;gt;a&amp;lt;/sub&amp;gt;) &amp;lt;!-- omit if not an acid or a base.  If several values, be clear --&amp;gt;&lt;br /&gt;
| {{{pKa}}}&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Acid_dissociation_constant Basicity] (p&#039;&#039;K&#039;&#039;&amp;lt;sub&amp;gt;b&amp;lt;/sub&amp;gt;) &amp;lt;!-- omit if not a base. If several values, be clear --&amp;gt;&lt;br /&gt;
| {{{pKb}}}&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Specific_rotation Chiral rotation &amp;lt;nowiki&amp;gt;[α]&amp;lt;/nowiki&amp;gt;&amp;lt;sub&amp;gt;D&amp;lt;/sub&amp;gt;] &amp;lt;!-- (Only include this for chiral compounds, indicate direction/enantiomer combo if known) --&amp;gt;&lt;br /&gt;
| {{{Rotation}}}°&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Viscosity Viscosity]&lt;br /&gt;
| {{{Viscosity}}} [[Poise|cP]] at 25°C &amp;lt;!-- Liquids only, omit if data unavailable. You may use [[Pascal second|Pa.s]] if you prefer --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Structure&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Orbital_hybridisation Molecular shape] &amp;lt;!-- for simple covalent molecules (omit for most large molecules, ionics and complexes) --&amp;gt;&lt;br /&gt;
| {{{Mol_Shape}}} &amp;lt;!-- e.g. trigonal bipyramidal --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Coordination_geometry Coordination&amp;lt;br /&amp;gt;geometry] &amp;lt;!-- for a metal complex or an ionic crystal, otherwise omit --&amp;gt;&lt;br /&gt;
| {{{Coordination}}} &amp;lt;!-- e.g. trigonal bipyramidal --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Crystal_structure Crystal structure] &amp;lt;!-- omit if not a solid --&amp;gt;&lt;br /&gt;
| {{{Crystal_Structure}}} &amp;lt;!-- e.g. [[triclinic]], [[monoclinic]], [[orthorhombic]], [[hexagonal]], [[rhombohedral|trigonal]], [[tetragonal]], [[cubic]], and mention &amp;quot;close packed&amp;quot; or similar.  You may also cite what class it belongs to, e.g. [[Cadmium_chloride#Crystal_structure|CdCl&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt;]]  --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [[Dipole#Molecular_dipoles|Dipole moment]]&lt;br /&gt;
| {{{DM}}} [[Debye|D]]&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Hazards &amp;lt;!--  Summary only- MSDS entry provides more complete information --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [[Material safety data sheet|MSDS]]&lt;br /&gt;
| [[{{PAGENAME}} (data page)#Material Safety Data Sheet|External MSDS]] &amp;lt;!-- please replace with proper link--&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| Main [[Worker safety and health|hazard]]s&lt;br /&gt;
| {{{Hazards}}} &amp;lt;!-- e.g. highly toxic, explosive, flammable, corrosive --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [[NFPA 704]]&lt;br /&gt;
| {{{NFPA}}}&amp;lt;!-- {{NFPA 704 | Health=4 | Flammability=4 | Reactivity=4 | Other=OX }} These are set on &amp;quot;very dangerous&amp;quot; as default- adjust according to actual values --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [[Flash point]]&lt;br /&gt;
| {{{Fp}}}°C&lt;br /&gt;
|-&lt;br /&gt;
| [[Risk and Safety Statements|R/S statement]]&lt;br /&gt;
| [[List of R-phrases|R]]: {{{R-S}}} &amp;lt;br /&amp;gt; [[List of S-phrases|S]]: ?&lt;br /&gt;
|-&lt;br /&gt;
| [[RTECS]] number&lt;br /&gt;
| {{{RTECS}}}&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | [[{{PAGENAME}} (data page)|Supplementary data page]]&lt;br /&gt;
|-&lt;br /&gt;
| [[{{PAGENAME}} (data page)#Structure and properties|Structure and&amp;lt;br /&amp;gt;properties]] &lt;br /&gt;
| [http://en.wikipedia.org/wiki/Refractive_index &#039;&#039;n&#039;&#039;], [http://en.wikipedia.org/wiki/Dielectric_constant ε&amp;lt;sub&amp;gt;r&amp;lt;/sub&amp;gt;], etc. &lt;br /&gt;
|-&lt;br /&gt;
| [[{{PAGENAME}} (data page)#Thermodynamic properties|Thermodynamic&amp;lt;br /&amp;gt;data]] &lt;br /&gt;
| Phase behaviour&amp;lt;br /&amp;gt;Solid, liquid, gas &lt;br /&gt;
|-&lt;br /&gt;
| [[{{PAGENAME}} (data page)#Spectral data|Spectral data]]&lt;br /&gt;
| [[UV/VIS spectroscopy|UV]], [[Infrared spectroscopy|IR]], [[nuclear magnetic resonance spectroscopy|NMR]], [[Mass spectrometry|MS]]&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Related compounds&lt;br /&gt;
|-&lt;br /&gt;
| Other [[Ion|anion]]s &amp;lt;!-- please omit if not applicable --&amp;gt;&lt;br /&gt;
| {{{Other_anion}}} &amp;lt;!-- Put in related anions e.g, iron(II) fluoride &amp;amp; iron(II) bromide if compound is iron(II) chloride --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| Other [[Ion|cation]]s &amp;lt;!-- please omit if not applicable --&amp;gt;&lt;br /&gt;
| {{{Ohter_cation}}} &amp;lt;!-- Put in other oxidation states of same element e.g. [[iron(III) chloride]], also for related metals such as [[manganese(II) chloride]], [[cobalt(II) chloride]], ruthenium(III) chloride--&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| Related compounds &lt;br /&gt;
&amp;lt;!-- A miscellaneous heading - use for covalent inorganics;  e.g. for PCl&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt; you would list PCl&amp;lt;sub&amp;gt;5&amp;lt;/sub&amp;gt;, POCl&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;, PF&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;, PBr&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;, NCl&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt; and AsCl&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;. &lt;br /&gt;
Please omit if not applicable --&amp;gt;&lt;br /&gt;
| {{{Relative_Compounds}}}&lt;br /&gt;
|-&lt;br /&gt;
| {{chembox header}} | &amp;lt;small&amp;gt;Except where noted otherwise, data are given for&amp;lt;br /&amp;gt; materials in their [[standard state|standard state (at 25&amp;amp;nbsp;°C, 100&amp;amp;nbsp;kPa)]]&amp;lt;br /&amp;gt;[[wikipedia:Chemical infobox|Infobox disclaimer and references]]&amp;lt;/small&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
|}&lt;br /&gt;
{{Chem-Data_Structure}}&lt;/div&gt;</summary>
		<author><name>Wwl06</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=Rohypnol&amp;diff=12050</id>
		<title>Rohypnol</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=Rohypnol&amp;diff=12050"/>
		<updated>2007-11-27T15:15:56Z</updated>

		<summary type="html">&lt;p&gt;Wwl06: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;br /&gt;
&amp;lt;noinclude&amp;gt;&lt;br /&gt;
&amp;lt;!-- This template has been defined after elaborate discussion in the Chemicals Wikiproject. Please do not add, deleted or otherwise change it unless after due discussion in [[wikipedia talk:WikiProject Chemicals]] --&amp;gt;&lt;br /&gt;
&amp;lt;/noinclude&amp;gt;{| class=&amp;quot;toccolours&amp;quot; border=&amp;quot;1&amp;quot; style=&amp;quot;float: right; clear: right; margin: 0 0 1em 1em; border-collapse: collapse; width: 280px&amp;quot;&lt;br /&gt;
! {{chembox header}} | {{PAGENAME}} &amp;lt;!-- replace if not identical with the article name --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image:{{PAGENAME}}.jpg|200px|{{PAGENAME}}]] &amp;lt;!-- replace if not identical with the pagename --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | General&lt;br /&gt;
|- &lt;br /&gt;
| [http://en.wikipedia.org/wiki/IUPAC Systematic name]&lt;br /&gt;
| {{{IUPACName}}}&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
| Other names&lt;br /&gt;
| {{{OtherNames}}}&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Chemical_formula Molecular formula]&lt;br /&gt;
| {{{Formula}}} &lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Chemical_file_format SMILES] &amp;lt;!-- mostly for organic compounds, omit otherwise --&amp;gt;&lt;br /&gt;
| {{{SMILES}}}&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Molar_mass Molar mass]&lt;br /&gt;
| {{{MolarMass}}}&lt;br /&gt;
|-&lt;br /&gt;
| Appearance&lt;br /&gt;
| {{{Appearance}}}&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/CAS_registry_number CAS number]&lt;br /&gt;
| {{{CASNo}}}&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Properties&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Density Density] &amp;amp; [http://en.wikipedia.org/wiki/Phase_%28matter%29 phase]&lt;br /&gt;
| {{{Density}}} g/cm³ &amp;lt;!-- ? g/cm³, solid / ? g/ml, liquid / ? g/l, gas --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Solubility Solubility in water]&lt;br /&gt;
| {{{Sol_Water}}} g/100 ml (25°C) &amp;lt;!--  at least put miscible with, not soluble in --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
&amp;lt;!-- | Other solvents e.g. [[ethanol]], [[acetone]] --&amp;gt;&lt;br /&gt;
&amp;lt;!-- | solubility info on other solvents --&amp;gt;&lt;br /&gt;
&amp;lt;!-- |- --&amp;gt;&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Melting_point Melting point]&lt;br /&gt;
| {{{Mp}}} K &amp;lt;!-- (mention any decomposition) --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Boiling_point Boiling point]&lt;br /&gt;
| {{{Bp}}} K&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Acid_dissociation_constant Acidity] (p&#039;&#039;K&#039;&#039;&amp;lt;sub&amp;gt;a&amp;lt;/sub&amp;gt;) &amp;lt;!-- omit if not an acid or a base.  If several values, be clear --&amp;gt;&lt;br /&gt;
| {{{pKa}}}&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Acid_dissociation_constant Basicity] (p&#039;&#039;K&#039;&#039;&amp;lt;sub&amp;gt;b&amp;lt;/sub&amp;gt;) &amp;lt;!-- omit if not a base. If several values, be clear --&amp;gt;&lt;br /&gt;
| {{{pKb}}}&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Specific_rotation Chiral rotation &amp;lt;nowiki&amp;gt;[α]&amp;lt;/nowiki&amp;gt;&amp;lt;sub&amp;gt;D&amp;lt;/sub&amp;gt;] &amp;lt;!-- (Only include this for chiral compounds, indicate direction/enantiomer combo if known) --&amp;gt;&lt;br /&gt;
| {{{Rotation}}}°&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Viscosity Viscosity]&lt;br /&gt;
| {{{Viscosity}}} [[Poise|cP]] at 25°C &amp;lt;!-- Liquids only, omit if data unavailable. You may use [[Pascal second|Pa.s]] if you prefer --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Structure&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Orbital_hybridisation Molecular shape] &amp;lt;!-- for simple covalent molecules (omit for most large molecules, ionics and complexes) --&amp;gt;&lt;br /&gt;
| {{{Mol_Shape}}} &amp;lt;!-- e.g. trigonal bipyramidal --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Coordination_geometry Coordination&amp;lt;br /&amp;gt;geometry] &amp;lt;!-- for a metal complex or an ionic crystal, otherwise omit --&amp;gt;&lt;br /&gt;
| {{{Coordination}}} &amp;lt;!-- e.g. trigonal bipyramidal --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Crystal_structure Crystal structure] &amp;lt;!-- omit if not a solid --&amp;gt;&lt;br /&gt;
| {{{Crystal_Structure}}} &amp;lt;!-- e.g. [[triclinic]], [[monoclinic]], [[orthorhombic]], [[hexagonal]], [[rhombohedral|trigonal]], [[tetragonal]], [[cubic]], and mention &amp;quot;close packed&amp;quot; or similar.  You may also cite what class it belongs to, e.g. [[Cadmium_chloride#Crystal_structure|CdCl&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt;]]  --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [[Dipole#Molecular_dipoles|Dipole moment]]&lt;br /&gt;
| {{{DM}}} [[Debye|D]]&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Hazards &amp;lt;!--  Summary only- MSDS entry provides more complete information --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [[Material safety data sheet|MSDS]]&lt;br /&gt;
| [[{{PAGENAME}} (data page)#Material Safety Data Sheet|External MSDS]] &amp;lt;!-- please replace with proper link--&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| Main [[Worker safety and health|hazard]]s&lt;br /&gt;
| {{{Hazards}}} &amp;lt;!-- e.g. highly toxic, explosive, flammable, corrosive --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [[NFPA 704]]&lt;br /&gt;
| {{{NFPA}}}&amp;lt;!-- {{NFPA 704 | Health=4 | Flammability=4 | Reactivity=4 | Other=OX }} These are set on &amp;quot;very dangerous&amp;quot; as default- adjust according to actual values --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [[Flash point]]&lt;br /&gt;
| {{{Fp}}}°C&lt;br /&gt;
|-&lt;br /&gt;
| [[Risk and Safety Statements|R/S statement]]&lt;br /&gt;
| [[List of R-phrases|R]]: {{{R-S}}} &amp;lt;br /&amp;gt; [[List of S-phrases|S]]: ?&lt;br /&gt;
|-&lt;br /&gt;
| [[RTECS]] number&lt;br /&gt;
| {{{RTECS}}}&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | [[{{PAGENAME}} (data page)|Supplementary data page]]&lt;br /&gt;
|-&lt;br /&gt;
| [[{{PAGENAME}} (data page)#Structure and properties|Structure and&amp;lt;br /&amp;gt;properties]] &lt;br /&gt;
| [http://en.wikipedia.org/wiki/Refractive_index &#039;&#039;n&#039;&#039;], [http://en.wikipedia.org/wiki/Dielectric_constant ε&amp;lt;sub&amp;gt;r&amp;lt;/sub&amp;gt;], etc. &lt;br /&gt;
|-&lt;br /&gt;
| [[{{PAGENAME}} (data page)#Thermodynamic properties|Thermodynamic&amp;lt;br /&amp;gt;data]] &lt;br /&gt;
| Phase behaviour&amp;lt;br /&amp;gt;Solid, liquid, gas &lt;br /&gt;
|-&lt;br /&gt;
| [[{{PAGENAME}} (data page)#Spectral data|Spectral data]]&lt;br /&gt;
| [[UV/VIS spectroscopy|UV]], [[Infrared spectroscopy|IR]], [[nuclear magnetic resonance spectroscopy|NMR]], [[Mass spectrometry|MS]]&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Related compounds&lt;br /&gt;
|-&lt;br /&gt;
| Other [[Ion|anion]]s &amp;lt;!-- please omit if not applicable --&amp;gt;&lt;br /&gt;
| {{{Other_anion}}} &amp;lt;!-- Put in related anions e.g, iron(II) fluoride &amp;amp; iron(II) bromide if compound is iron(II) chloride --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| Other [[Ion|cation]]s &amp;lt;!-- please omit if not applicable --&amp;gt;&lt;br /&gt;
| {{{Ohter_cation}}} &amp;lt;!-- Put in other oxidation states of same element e.g. [[iron(III) chloride]], also for related metals such as [[manganese(II) chloride]], [[cobalt(II) chloride]], ruthenium(III) chloride--&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| Related compounds &lt;br /&gt;
&amp;lt;!-- A miscellaneous heading - use for covalent inorganics;  e.g. for PCl&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt; you would list PCl&amp;lt;sub&amp;gt;5&amp;lt;/sub&amp;gt;, POCl&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;, PF&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;, PBr&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;, NCl&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt; and AsCl&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;. &lt;br /&gt;
Please omit if not applicable --&amp;gt;&lt;br /&gt;
| {{{Relative_Compounds}}}&lt;br /&gt;
|-&lt;br /&gt;
| {{chembox header}} | &amp;lt;small&amp;gt;Except where noted otherwise, data are given for&amp;lt;br /&amp;gt; materials in their [[standard state|standard state (at 25&amp;amp;nbsp;°C, 100&amp;amp;nbsp;kPa)]]&amp;lt;br /&amp;gt;[[wikipedia:Chemical infobox|Infobox disclaimer and references]]&amp;lt;/small&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
|}&lt;br /&gt;
{{Chem-Data_Structure}}&lt;/div&gt;</summary>
		<author><name>Wwl06</name></author>
	</entry>
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