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	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It:Linalool&amp;diff=5028</id>
		<title>It:Linalool</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It:Linalool&amp;diff=5028"/>
		<updated>2006-11-08T15:39:24Z</updated>

		<summary type="html">&lt;p&gt;Jy405: /* References */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;==Introduction==&lt;br /&gt;
&#039;&#039;Lavender&#039;&#039; is a shrubby plant in the mint family with about 25-30 species. It is native from the Mediterranean region south to tropical Afric and the east to India. The aromatic smell is found in all parts of the shrub, but the essential oil is only produced from the flowers and flower-stalks. The lavender flower oil is a complex mixture compounds containing &#039;&#039;linalool&#039;&#039;, &#039;&#039;linalyl acetate&#039;&#039;, &#039;&#039;1, 8-cineole&#039;&#039;, &#039;&#039;β-ocimene&#039;&#039; and so on.&lt;br /&gt;
&lt;br /&gt;
[[Image:Lavender.jpg]]&lt;br /&gt;
&lt;br /&gt;
A picture of Lavender flower.&lt;br /&gt;
&lt;br /&gt;
==Linalool==&lt;br /&gt;
&#039;&#039;&#039;Linalool&#039;&#039;&#039;is a colourless fragrant liquid which can be found in many essential oil. As a fragrance, it is used in many soaps, detergents, creams, lotions, shampoos and it is a chemical intermediate in the formation of Vitamin E. It is also an insecticide which is safe to humans. &lt;br /&gt;
&lt;br /&gt;
[[Image:2D-structure_of_Linalool.gif]] &lt;br /&gt;
2D-strcture of a Linalool Molecule&lt;br /&gt;
&lt;br /&gt;
&amp;lt;jmol&amp;gt;&lt;br /&gt;
&amp;lt;jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;size&amp;gt;300&amp;lt;/size&amp;gt;&lt;br /&gt;
&amp;lt;color&amp;gt;silver&amp;lt;/color&amp;gt;&lt;br /&gt;
&amp;lt;script&amp;gt;zoom 120; cpk off;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;HEADER    NONAME 06-Nov-06                                              NONE   1&lt;br /&gt;
TITLE                                                                   NONE   2&lt;br /&gt;
AUTHOR    WWW daemon apache                                             NONE   3&lt;br /&gt;
REVDAT   1  06-Nov-06     0                                             NONE   4&lt;br /&gt;
ATOM      1  C           0      -3.030   1.372   0.117  0.00  0.00           C+0&lt;br /&gt;
ATOM      2  C           0      -3.012  -0.132   0.023  0.00  0.00           C+0&lt;br /&gt;
ATOM      3  C           0      -1.921  -0.752  -0.353  0.00  0.00           C+0&lt;br /&gt;
ATOM      4  C           0      -0.650   0.027  -0.573  0.00  0.00           C+0&lt;br /&gt;
ATOM      5  C           0       0.473  -0.580   0.272  0.00  0.00           C+0&lt;br /&gt;
ATOM      6  C           0       1.763   0.211   0.049  0.00  0.00           C+0&lt;br /&gt;
ATOM      7  C           0       1.546   1.668   0.460  0.00  0.00           C+0&lt;br /&gt;
ATOM      8  C           0       2.869  -0.387   0.880  0.00  0.00           C+0&lt;br /&gt;
ATOM      9  C           0       3.947  -0.853   0.300  0.00  0.00           C+0&lt;br /&gt;
ATOM     10  O           0       2.123   0.155  -1.333  0.00  0.00           O+0&lt;br /&gt;
ATOM     11  C           0      -4.249  -0.923   0.362  0.00  0.00           C+0&lt;br /&gt;
ATOM     12  H           0      -2.720   1.799  -0.837  0.00  0.00           H+0&lt;br /&gt;
ATOM     13  H           0      -4.039   1.709   0.356  0.00  0.00           H+0&lt;br /&gt;
ATOM     14  H           0      -2.344   1.695   0.900  0.00  0.00           H+0&lt;br /&gt;
ATOM     15  H           0      -1.932  -1.821  -0.506  0.00  0.00           H+0&lt;br /&gt;
ATOM     16  H           0      -0.375  -0.016  -1.627  0.00  0.00           H+0&lt;br /&gt;
ATOM     17  H           0      -0.804   1.065  -0.279  0.00  0.00           H+0&lt;br /&gt;
ATOM     18  H           0       0.198  -0.537   1.326  0.00  0.00           H+0&lt;br /&gt;
ATOM     19  H           0       0.627  -1.618  -0.022  0.00  0.00           H+0&lt;br /&gt;
ATOM     20  H           0       1.272   1.711   1.514  0.00  0.00           H+0&lt;br /&gt;
ATOM     21  H           0       2.466   2.232   0.301  0.00  0.00           H+0&lt;br /&gt;
ATOM     22  H           0       0.747   2.101  -0.141  0.00  0.00           H+0&lt;br /&gt;
ATOM     23  H           0       2.772  -0.431   1.955  0.00  0.00           H+0&lt;br /&gt;
ATOM     24  H           0       4.739  -1.281   0.896  0.00  0.00           H+0&lt;br /&gt;
ATOM     25  H           0       4.043  -0.809  -0.775  0.00  0.00           H+0&lt;br /&gt;
ATOM     26  H           0       2.251  -0.779  -1.551  0.00  0.00           H+0&lt;br /&gt;
ATOM     27  H           0      -4.046  -1.987   0.237  0.00  0.00           H+0&lt;br /&gt;
ATOM     28  H           0      -4.534  -0.727   1.396  0.00  0.00           H+0&lt;br /&gt;
ATOM     29  H           0      -5.062  -0.628  -0.301  0.00  0.00           H+0&lt;br /&gt;
CONECT    1    2   12   13   14                                         NONE  34&lt;br /&gt;
CONECT    2    1    3   11    0                                         NONE  35&lt;br /&gt;
CONECT    3    2    4   15    0                                         NONE  36&lt;br /&gt;
CONECT    4    3    5   16   17                                         NONE  37&lt;br /&gt;
CONECT    5    4    6   18   19                                         NONE  38&lt;br /&gt;
CONECT    6    5    7    8   10                                         NONE  39&lt;br /&gt;
CONECT    7    6   20   21   22                                         NONE  40&lt;br /&gt;
CONECT    8    6    9   23    0                                         NONE  41&lt;br /&gt;
CONECT    9    8   24   25    0                                         NONE  42&lt;br /&gt;
CONECT   10    6   26    0    0                                         NONE  43&lt;br /&gt;
CONECT   11    2   27   28   29                                         NONE  44&lt;br /&gt;
END                                                                     NONE  45&lt;br /&gt;
&amp;lt;/inlineContents&amp;gt;&lt;br /&gt;
&amp;lt;/jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;/jmol&amp;gt;&lt;br /&gt;
3D -Structure of A Linalool Molecule&lt;br /&gt;
&lt;br /&gt;
{| border=&amp;quot;1&amp;quot;&lt;br /&gt;
|+ The table&#039;s caption&lt;br /&gt;
!  !!&lt;br /&gt;
|-&lt;br /&gt;
! Einecs Number&lt;br /&gt;
| 201-134-4 ||&lt;br /&gt;
|-&lt;br /&gt;
! CAS Number&lt;br /&gt;
|78-70-6 ||&lt;br /&gt;
|-&lt;br /&gt;
! Chemical Name&lt;br /&gt;
|Linalool ||&lt;br /&gt;
|-&lt;br /&gt;
! Autoname&lt;br /&gt;
|&#039;&#039;3,7-Dimethyl-1,6-octadien-3-ol&#039;&#039; ||&lt;br /&gt;
|-&lt;br /&gt;
! Molecular Formula&lt;br /&gt;
|C10H18O||&lt;br /&gt;
|-&lt;br /&gt;
! Molecular Weight&lt;br /&gt;
|154.25 g/mol||&lt;br /&gt;
|-&lt;br /&gt;
! Physical State&lt;br /&gt;
|Clear to slightly yellow liquid||&lt;br /&gt;
|-&lt;br /&gt;
! Boiling Point&lt;br /&gt;
|198-200C||&lt;br /&gt;
|-&lt;br /&gt;
! Solubility in Water&lt;br /&gt;
|Insoluble||&lt;br /&gt;
|-&lt;br /&gt;
! Flash Point&lt;br /&gt;
|75C||&lt;br /&gt;
|-&lt;br /&gt;
! Toxicity&lt;br /&gt;
|Oral rat LD50: 2790 mg/kg||&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
==Synthesis of linalool==&lt;br /&gt;
Linalool is an anyclic alcohol. It has a sweet, pleasant fragrance and is one of the most frequently encountered floral scent compounds. Linalool has two enantiomeric forms (R) - linalool and (S) - linalool corresponds to the chiral properties of its hydroxylated third carbon. Traditionally, linalool was obtained from α- or β-pinene. The most modern synthesis start with &#039;&#039;2-methyl-2-hepten-6-one&#039;&#039; and proceed via base-calalyzed ethynylation with acetylene to dehydrolinalool, yielding linalool through hydrogenation of the triple bond in the presence of a palladium-carbon catalyst.&lt;br /&gt;
&lt;br /&gt;
[[Image:Synthesis_of_Linalool_Molecule.gif]]&lt;br /&gt;
&lt;br /&gt;
The process of sysnthesising a linalool molecule.&lt;br /&gt;
&lt;br /&gt;
==Uses of Lavender oil==&lt;br /&gt;
Generally its modern use is for aromatherapy. The research in lab showed that it helped in the reduction of advanced  mammory tumors in lab rats. Some other researches such as potential breast, ovarian, pancreatic, liver, and prostate cancer treatments are on-going.&lt;br /&gt;
Some advocates of alternative medicine claim that lavender oil can be used in a variety of variety.&lt;br /&gt;
 •	Cream: Add a few drops of oil to chamomile cream for eczema.&lt;br /&gt;
 •	Lotion: Add a few drops of oil to a little water for sunburn or scalds.&lt;br /&gt;
 •	Chest Rub: Add 1 ml oil and 5 drops chamomile oil to 10 ml carrier oil for asthmatic and bronchitic spasm.&lt;br /&gt;
 •	Hair Rinse: Dilute 5-10 drops of oil in water for lice, or use a few drops of neat oil on a fine comb for nits.&lt;br /&gt;
 •	Oil Apply undiluted to insect bites and stings: Dilute 10 drops oil in 25 ml carrier oil for sunstroke or to help prevent sunburn. &lt;br /&gt;
 •	Massage Oil: Dilute 1 ml &#039;lavender oil&#039; in 25 ml carrier oil, and massage into painful muscles.Dilute 10 drops in 25 ml carrier oil and massage into the temples and nape of the neck for tension headaches or at the first hint of a migraine.&lt;br /&gt;
&lt;br /&gt;
==Side Effects of Lavender oil==&lt;br /&gt;
A July 1, 2006 article in Science News stated that lavender oil had been implicated in abnormal development of the breasts in young boys.  Boys and girls are particularly sensitive to estrogenic and androgenic compounds because their sex hormone levels are low prior to puberty.There are identified hormonally active compounds in lavender oil which may be contributing to the increase incidence of early breast development in girls and enlarged breasts in boys.&lt;br /&gt;
&lt;br /&gt;
==References==&lt;br /&gt;
1.	&#039;&#039;http://en.wikipedia.org/wiki/Lavender&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
2.	&#039;&#039;http://www.umich.edu/~chemh215/CHEM216/HonorsCup/hcproposal/251__A.pdf&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
3.      &#039;&#039;http://www.linguasphere.org/dictionary/n-42188-linalool.html&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
4.      &#039;&#039;http://www.chemicalland21.com/specialtychem/perchem/LINALOOL.htm&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
5.      &#039;&#039;http://www.molecular-networks.com/online_demos/corina_demo.html&#039;&#039;&lt;/div&gt;</summary>
		<author><name>Jy405</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It:Linalool&amp;diff=5027</id>
		<title>It:Linalool</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It:Linalool&amp;diff=5027"/>
		<updated>2006-11-08T15:25:33Z</updated>

		<summary type="html">&lt;p&gt;Jy405: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;==Introduction==&lt;br /&gt;
&#039;&#039;Lavender&#039;&#039; is a shrubby plant in the mint family with about 25-30 species. It is native from the Mediterranean region south to tropical Afric and the east to India. The aromatic smell is found in all parts of the shrub, but the essential oil is only produced from the flowers and flower-stalks. The lavender flower oil is a complex mixture compounds containing &#039;&#039;linalool&#039;&#039;, &#039;&#039;linalyl acetate&#039;&#039;, &#039;&#039;1, 8-cineole&#039;&#039;, &#039;&#039;β-ocimene&#039;&#039; and so on.&lt;br /&gt;
&lt;br /&gt;
[[Image:Lavender.jpg]]&lt;br /&gt;
&lt;br /&gt;
A picture of Lavender flower.&lt;br /&gt;
&lt;br /&gt;
==Linalool==&lt;br /&gt;
&#039;&#039;&#039;Linalool&#039;&#039;&#039;is a colourless fragrant liquid which can be found in many essential oil. As a fragrance, it is used in many soaps, detergents, creams, lotions, shampoos and it is a chemical intermediate in the formation of Vitamin E. It is also an insecticide which is safe to humans. &lt;br /&gt;
&lt;br /&gt;
[[Image:2D-structure_of_Linalool.gif]] &lt;br /&gt;
2D-strcture of a Linalool Molecule&lt;br /&gt;
&lt;br /&gt;
&amp;lt;jmol&amp;gt;&lt;br /&gt;
&amp;lt;jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;size&amp;gt;300&amp;lt;/size&amp;gt;&lt;br /&gt;
&amp;lt;color&amp;gt;silver&amp;lt;/color&amp;gt;&lt;br /&gt;
&amp;lt;script&amp;gt;zoom 120; cpk off;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;HEADER    NONAME 06-Nov-06                                              NONE   1&lt;br /&gt;
TITLE                                                                   NONE   2&lt;br /&gt;
AUTHOR    WWW daemon apache                                             NONE   3&lt;br /&gt;
REVDAT   1  06-Nov-06     0                                             NONE   4&lt;br /&gt;
ATOM      1  C           0      -3.030   1.372   0.117  0.00  0.00           C+0&lt;br /&gt;
ATOM      2  C           0      -3.012  -0.132   0.023  0.00  0.00           C+0&lt;br /&gt;
ATOM      3  C           0      -1.921  -0.752  -0.353  0.00  0.00           C+0&lt;br /&gt;
ATOM      4  C           0      -0.650   0.027  -0.573  0.00  0.00           C+0&lt;br /&gt;
ATOM      5  C           0       0.473  -0.580   0.272  0.00  0.00           C+0&lt;br /&gt;
ATOM      6  C           0       1.763   0.211   0.049  0.00  0.00           C+0&lt;br /&gt;
ATOM      7  C           0       1.546   1.668   0.460  0.00  0.00           C+0&lt;br /&gt;
ATOM      8  C           0       2.869  -0.387   0.880  0.00  0.00           C+0&lt;br /&gt;
ATOM      9  C           0       3.947  -0.853   0.300  0.00  0.00           C+0&lt;br /&gt;
ATOM     10  O           0       2.123   0.155  -1.333  0.00  0.00           O+0&lt;br /&gt;
ATOM     11  C           0      -4.249  -0.923   0.362  0.00  0.00           C+0&lt;br /&gt;
ATOM     12  H           0      -2.720   1.799  -0.837  0.00  0.00           H+0&lt;br /&gt;
ATOM     13  H           0      -4.039   1.709   0.356  0.00  0.00           H+0&lt;br /&gt;
ATOM     14  H           0      -2.344   1.695   0.900  0.00  0.00           H+0&lt;br /&gt;
ATOM     15  H           0      -1.932  -1.821  -0.506  0.00  0.00           H+0&lt;br /&gt;
ATOM     16  H           0      -0.375  -0.016  -1.627  0.00  0.00           H+0&lt;br /&gt;
ATOM     17  H           0      -0.804   1.065  -0.279  0.00  0.00           H+0&lt;br /&gt;
ATOM     18  H           0       0.198  -0.537   1.326  0.00  0.00           H+0&lt;br /&gt;
ATOM     19  H           0       0.627  -1.618  -0.022  0.00  0.00           H+0&lt;br /&gt;
ATOM     20  H           0       1.272   1.711   1.514  0.00  0.00           H+0&lt;br /&gt;
ATOM     21  H           0       2.466   2.232   0.301  0.00  0.00           H+0&lt;br /&gt;
ATOM     22  H           0       0.747   2.101  -0.141  0.00  0.00           H+0&lt;br /&gt;
ATOM     23  H           0       2.772  -0.431   1.955  0.00  0.00           H+0&lt;br /&gt;
ATOM     24  H           0       4.739  -1.281   0.896  0.00  0.00           H+0&lt;br /&gt;
ATOM     25  H           0       4.043  -0.809  -0.775  0.00  0.00           H+0&lt;br /&gt;
ATOM     26  H           0       2.251  -0.779  -1.551  0.00  0.00           H+0&lt;br /&gt;
ATOM     27  H           0      -4.046  -1.987   0.237  0.00  0.00           H+0&lt;br /&gt;
ATOM     28  H           0      -4.534  -0.727   1.396  0.00  0.00           H+0&lt;br /&gt;
ATOM     29  H           0      -5.062  -0.628  -0.301  0.00  0.00           H+0&lt;br /&gt;
CONECT    1    2   12   13   14                                         NONE  34&lt;br /&gt;
CONECT    2    1    3   11    0                                         NONE  35&lt;br /&gt;
CONECT    3    2    4   15    0                                         NONE  36&lt;br /&gt;
CONECT    4    3    5   16   17                                         NONE  37&lt;br /&gt;
CONECT    5    4    6   18   19                                         NONE  38&lt;br /&gt;
CONECT    6    5    7    8   10                                         NONE  39&lt;br /&gt;
CONECT    7    6   20   21   22                                         NONE  40&lt;br /&gt;
CONECT    8    6    9   23    0                                         NONE  41&lt;br /&gt;
CONECT    9    8   24   25    0                                         NONE  42&lt;br /&gt;
CONECT   10    6   26    0    0                                         NONE  43&lt;br /&gt;
CONECT   11    2   27   28   29                                         NONE  44&lt;br /&gt;
END                                                                     NONE  45&lt;br /&gt;
&amp;lt;/inlineContents&amp;gt;&lt;br /&gt;
&amp;lt;/jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;/jmol&amp;gt;&lt;br /&gt;
3D -Structure of A Linalool Molecule&lt;br /&gt;
&lt;br /&gt;
{| border=&amp;quot;1&amp;quot;&lt;br /&gt;
|+ The table&#039;s caption&lt;br /&gt;
!  !!&lt;br /&gt;
|-&lt;br /&gt;
! Einecs Number&lt;br /&gt;
| 201-134-4 ||&lt;br /&gt;
|-&lt;br /&gt;
! CAS Number&lt;br /&gt;
|78-70-6 ||&lt;br /&gt;
|-&lt;br /&gt;
! Chemical Name&lt;br /&gt;
|Linalool ||&lt;br /&gt;
|-&lt;br /&gt;
! Autoname&lt;br /&gt;
|&#039;&#039;3,7-Dimethyl-1,6-octadien-3-ol&#039;&#039; ||&lt;br /&gt;
|-&lt;br /&gt;
! Molecular Formula&lt;br /&gt;
|C10H18O||&lt;br /&gt;
|-&lt;br /&gt;
! Molecular Weight&lt;br /&gt;
|154.25 g/mol||&lt;br /&gt;
|-&lt;br /&gt;
! Physical State&lt;br /&gt;
|Clear to slightly yellow liquid||&lt;br /&gt;
|-&lt;br /&gt;
! Boiling Point&lt;br /&gt;
|198-200C||&lt;br /&gt;
|-&lt;br /&gt;
! Solubility in Water&lt;br /&gt;
|Insoluble||&lt;br /&gt;
|-&lt;br /&gt;
! Flash Point&lt;br /&gt;
|75C||&lt;br /&gt;
|-&lt;br /&gt;
! Toxicity&lt;br /&gt;
|Oral rat LD50: 2790 mg/kg||&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
==Synthesis of linalool==&lt;br /&gt;
Linalool is an anyclic alcohol. It has a sweet, pleasant fragrance and is one of the most frequently encountered floral scent compounds. Linalool has two enantiomeric forms (R) - linalool and (S) - linalool corresponds to the chiral properties of its hydroxylated third carbon. Traditionally, linalool was obtained from α- or β-pinene. The most modern synthesis start with &#039;&#039;2-methyl-2-hepten-6-one&#039;&#039; and proceed via base-calalyzed ethynylation with acetylene to dehydrolinalool, yielding linalool through hydrogenation of the triple bond in the presence of a palladium-carbon catalyst.&lt;br /&gt;
&lt;br /&gt;
[[Image:Synthesis_of_Linalool_Molecule.gif]]&lt;br /&gt;
&lt;br /&gt;
The process of sysnthesising a linalool molecule.&lt;br /&gt;
&lt;br /&gt;
==Uses of Lavender oil==&lt;br /&gt;
Generally its modern use is for aromatherapy. The research in lab showed that it helped in the reduction of advanced  mammory tumors in lab rats. Some other researches such as potential breast, ovarian, pancreatic, liver, and prostate cancer treatments are on-going.&lt;br /&gt;
Some advocates of alternative medicine claim that lavender oil can be used in a variety of variety.&lt;br /&gt;
 •	Cream: Add a few drops of oil to chamomile cream for eczema.&lt;br /&gt;
 •	Lotion: Add a few drops of oil to a little water for sunburn or scalds.&lt;br /&gt;
 •	Chest Rub: Add 1 ml oil and 5 drops chamomile oil to 10 ml carrier oil for asthmatic and bronchitic spasm.&lt;br /&gt;
 •	Hair Rinse: Dilute 5-10 drops of oil in water for lice, or use a few drops of neat oil on a fine comb for nits.&lt;br /&gt;
 •	Oil Apply undiluted to insect bites and stings: Dilute 10 drops oil in 25 ml carrier oil for sunstroke or to help prevent sunburn. &lt;br /&gt;
 •	Massage Oil: Dilute 1 ml &#039;lavender oil&#039; in 25 ml carrier oil, and massage into painful muscles.Dilute 10 drops in 25 ml carrier oil and massage into the temples and nape of the neck for tension headaches or at the first hint of a migraine.&lt;br /&gt;
&lt;br /&gt;
==Side Effects of Lavender oil==&lt;br /&gt;
A July 1, 2006 article in Science News stated that lavender oil had been implicated in abnormal development of the breasts in young boys.  Boys and girls are particularly sensitive to estrogenic and androgenic compounds because their sex hormone levels are low prior to puberty.There are identified hormonally active compounds in lavender oil which may be contributing to the increase incidence of early breast development in girls and enlarged breasts in boys.&lt;br /&gt;
&lt;br /&gt;
==References==&lt;br /&gt;
1.	&#039;&#039;http://en.wikipedia.org/wiki/Lavender&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
2.	&#039;&#039;http://www.umich.edu/~chemh215/CHEM216/HonorsCup/hcproposal/251__A.pdf&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
3.      &#039;&#039;http://www.linguasphere.org/dictionary/n-42188-linalool.html&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
4.      &#039;&#039;http://www.chemicalland21.com/specialtychem/perchem/LINALOOL.htm&#039;&#039;&lt;/div&gt;</summary>
		<author><name>Jy405</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It:Linalool&amp;diff=5025</id>
		<title>It:Linalool</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It:Linalool&amp;diff=5025"/>
		<updated>2006-11-08T15:15:25Z</updated>

		<summary type="html">&lt;p&gt;Jy405: References&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;==Introduction==&lt;br /&gt;
Lavender is a shrubby plant in the mint family with about 25-30 species. It is native from the Mediterranean region south to tropical Afric and the east to India. The aromatic smell is found in all parts of the shrub, but the essential oil is only produced from the flowers and flower-stalks. The lavender flower oil is a complex mixture compounds containing linalool, linalyl acetate, 1, 8-cineole, β-ocimene and so on.&lt;br /&gt;
&lt;br /&gt;
[[Image:Lavender.jpg]]&lt;br /&gt;
&lt;br /&gt;
A picture of Lavender flower.&lt;br /&gt;
&lt;br /&gt;
==Linalool==&lt;br /&gt;
Linalool is a colourless fragrant liquid which can be found in many essential oil. As a fragrance, it is used in many soaps, detergents, creams, lotions, shampoos and it is a chemical intermediate in the formation of Vitamin E. It is also an insecticide which is safe to humans. &lt;br /&gt;
&lt;br /&gt;
[[Image:2D-structure_of_Linalool.gif]] &lt;br /&gt;
2D-strcture of a Linalool Molecule&lt;br /&gt;
&lt;br /&gt;
&amp;lt;jmol&amp;gt;&lt;br /&gt;
&amp;lt;jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;size&amp;gt;300&amp;lt;/size&amp;gt;&lt;br /&gt;
&amp;lt;color&amp;gt;silver&amp;lt;/color&amp;gt;&lt;br /&gt;
&amp;lt;script&amp;gt;zoom 120; cpk off;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;HEADER    NONAME 06-Nov-06                                              NONE   1&lt;br /&gt;
TITLE                                                                   NONE   2&lt;br /&gt;
AUTHOR    WWW daemon apache                                             NONE   3&lt;br /&gt;
REVDAT   1  06-Nov-06     0                                             NONE   4&lt;br /&gt;
ATOM      1  C           0      -3.030   1.372   0.117  0.00  0.00           C+0&lt;br /&gt;
ATOM      2  C           0      -3.012  -0.132   0.023  0.00  0.00           C+0&lt;br /&gt;
ATOM      3  C           0      -1.921  -0.752  -0.353  0.00  0.00           C+0&lt;br /&gt;
ATOM      4  C           0      -0.650   0.027  -0.573  0.00  0.00           C+0&lt;br /&gt;
ATOM      5  C           0       0.473  -0.580   0.272  0.00  0.00           C+0&lt;br /&gt;
ATOM      6  C           0       1.763   0.211   0.049  0.00  0.00           C+0&lt;br /&gt;
ATOM      7  C           0       1.546   1.668   0.460  0.00  0.00           C+0&lt;br /&gt;
ATOM      8  C           0       2.869  -0.387   0.880  0.00  0.00           C+0&lt;br /&gt;
ATOM      9  C           0       3.947  -0.853   0.300  0.00  0.00           C+0&lt;br /&gt;
ATOM     10  O           0       2.123   0.155  -1.333  0.00  0.00           O+0&lt;br /&gt;
ATOM     11  C           0      -4.249  -0.923   0.362  0.00  0.00           C+0&lt;br /&gt;
ATOM     12  H           0      -2.720   1.799  -0.837  0.00  0.00           H+0&lt;br /&gt;
ATOM     13  H           0      -4.039   1.709   0.356  0.00  0.00           H+0&lt;br /&gt;
ATOM     14  H           0      -2.344   1.695   0.900  0.00  0.00           H+0&lt;br /&gt;
ATOM     15  H           0      -1.932  -1.821  -0.506  0.00  0.00           H+0&lt;br /&gt;
ATOM     16  H           0      -0.375  -0.016  -1.627  0.00  0.00           H+0&lt;br /&gt;
ATOM     17  H           0      -0.804   1.065  -0.279  0.00  0.00           H+0&lt;br /&gt;
ATOM     18  H           0       0.198  -0.537   1.326  0.00  0.00           H+0&lt;br /&gt;
ATOM     19  H           0       0.627  -1.618  -0.022  0.00  0.00           H+0&lt;br /&gt;
ATOM     20  H           0       1.272   1.711   1.514  0.00  0.00           H+0&lt;br /&gt;
ATOM     21  H           0       2.466   2.232   0.301  0.00  0.00           H+0&lt;br /&gt;
ATOM     22  H           0       0.747   2.101  -0.141  0.00  0.00           H+0&lt;br /&gt;
ATOM     23  H           0       2.772  -0.431   1.955  0.00  0.00           H+0&lt;br /&gt;
ATOM     24  H           0       4.739  -1.281   0.896  0.00  0.00           H+0&lt;br /&gt;
ATOM     25  H           0       4.043  -0.809  -0.775  0.00  0.00           H+0&lt;br /&gt;
ATOM     26  H           0       2.251  -0.779  -1.551  0.00  0.00           H+0&lt;br /&gt;
ATOM     27  H           0      -4.046  -1.987   0.237  0.00  0.00           H+0&lt;br /&gt;
ATOM     28  H           0      -4.534  -0.727   1.396  0.00  0.00           H+0&lt;br /&gt;
ATOM     29  H           0      -5.062  -0.628  -0.301  0.00  0.00           H+0&lt;br /&gt;
CONECT    1    2   12   13   14                                         NONE  34&lt;br /&gt;
CONECT    2    1    3   11    0                                         NONE  35&lt;br /&gt;
CONECT    3    2    4   15    0                                         NONE  36&lt;br /&gt;
CONECT    4    3    5   16   17                                         NONE  37&lt;br /&gt;
CONECT    5    4    6   18   19                                         NONE  38&lt;br /&gt;
CONECT    6    5    7    8   10                                         NONE  39&lt;br /&gt;
CONECT    7    6   20   21   22                                         NONE  40&lt;br /&gt;
CONECT    8    6    9   23    0                                         NONE  41&lt;br /&gt;
CONECT    9    8   24   25    0                                         NONE  42&lt;br /&gt;
CONECT   10    6   26    0    0                                         NONE  43&lt;br /&gt;
CONECT   11    2   27   28   29                                         NONE  44&lt;br /&gt;
END                                                                     NONE  45&lt;br /&gt;
&amp;lt;/inlineContents&amp;gt;&lt;br /&gt;
&amp;lt;/jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;/jmol&amp;gt;&lt;br /&gt;
3D -Structure of A Linalool Molecule&lt;br /&gt;
&lt;br /&gt;
{| border=&amp;quot;1&amp;quot;&lt;br /&gt;
|+ The table&#039;s caption&lt;br /&gt;
!  !!&lt;br /&gt;
|-&lt;br /&gt;
! Einecs Number&lt;br /&gt;
| 201-134-4 ||&lt;br /&gt;
|-&lt;br /&gt;
! CAS Number&lt;br /&gt;
|78-70-6 ||&lt;br /&gt;
|-&lt;br /&gt;
! Chemical Name&lt;br /&gt;
|Linalool ||&lt;br /&gt;
|-&lt;br /&gt;
! Autoname&lt;br /&gt;
|3,7-Dimethyl-1,6-octadien-3-ol ||&lt;br /&gt;
|-&lt;br /&gt;
! Molecular Formula&lt;br /&gt;
|C10H18O||&lt;br /&gt;
|-&lt;br /&gt;
! Molecular Weight&lt;br /&gt;
|154.25 g/mol||&lt;br /&gt;
|-&lt;br /&gt;
! Physical State&lt;br /&gt;
|Clear to slightly yellow liquid||&lt;br /&gt;
|-&lt;br /&gt;
! Boiling Point&lt;br /&gt;
|198-200C||&lt;br /&gt;
|-&lt;br /&gt;
! Solubility in Water&lt;br /&gt;
|Insoluble||&lt;br /&gt;
|-&lt;br /&gt;
! Flash Point&lt;br /&gt;
|75C||&lt;br /&gt;
|-&lt;br /&gt;
! Toxicity&lt;br /&gt;
|Oral rat LD50: 2790 mg/kg||&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
==Synthesis of linalool==&lt;br /&gt;
Linalool is an anyclic alcohol. It has a sweet, pleasant fragrance and is one of the most frequently encountered floral scent compounds. Linalool has two enantiomeric forms (R) - linalool and (S) - linalool corresponds to the chiral properties of its hydroxylated third carbon. Traditionally, linalool was obtained from α- or β-pinene. The most modern synthesis start with 2-methyl-2-hepten-6-one and proceed via base-calalyzed ethynylation with acetylene to dehydrolinalool, yielding linalool through hydrogenation of the triple bond in the presence of a palladium-carbon catalyst.&lt;br /&gt;
&lt;br /&gt;
[[Image:Synthesis_of_Linalool_Molecule.gif]]&lt;br /&gt;
&lt;br /&gt;
The process of sysnthesising a linalool molecule.&lt;br /&gt;
&lt;br /&gt;
==Uses of Lavender oil==&lt;br /&gt;
Generally its modern use is for aromatherapy. The research in lab showed that it helped in the reduction of advanced  mammory tumors in lab rats. Some other researches such as potential breast, ovarian, pancreatic, liver, and prostate cancer treatments are on-going.&lt;br /&gt;
Some advocates of alternative medicine claim that lavender oil can be used in a variety of variety.&lt;br /&gt;
 •	Cream: Add a few drops of oil to chamomile cream for eczema.&lt;br /&gt;
 •	Lotion: Add a few drops of oil to a little water for sunburn or scalds.&lt;br /&gt;
 •	Chest Rub: Add 1 ml oil and 5 drops chamomile oil to 10 ml carrier oil for asthmatic and bronchitic spasm.&lt;br /&gt;
 •	Hair Rinse: Dilute 5-10 drops of oil in water for lice, or use a few drops of neat oil on a fine comb for nits.&lt;br /&gt;
 •	Oil Apply undiluted to insect bites and stings: Dilute 10 drops oil in 25 ml carrier oil for sunstroke or to help prevent sunburn. &lt;br /&gt;
 •	Massage Oil: Dilute 1 ml &#039;lavender oil&#039; in 25 ml carrier oil, and massage into painful muscles.Dilute 10 drops in 25 ml carrier oil and massage into the temples and nape of the neck for tension headaches or at the first hint of a migraine.&lt;br /&gt;
&lt;br /&gt;
==Side Effects of Lavender oil==&lt;br /&gt;
A July 1, 2006 article in Science News stated that lavender oil had been implicated in abnormal development of the breasts in young boys.  Boys and girls are particularly sensitive to estrogenic and androgenic compounds because their sex hormone levels are low prior to puberty.There are identified hormonally active compounds in lavender oil which may be contributing to the increase incidence of early breast development in girls and enlarged breasts in boys.&lt;br /&gt;
&lt;br /&gt;
==References==&lt;br /&gt;
1.	http://en.wikipedia.org/wiki/Lavender&lt;br /&gt;
&lt;br /&gt;
2.	http://www.umich.edu/~chemh215/CHEM216/HonorsCup/hcproposal/251__A.pdf&lt;br /&gt;
&lt;br /&gt;
3.      http://www.linguasphere.org/dictionary/n-42188-linalool.html&lt;br /&gt;
&lt;br /&gt;
4.      http://www.chemicalland21.com/specialtychem/perchem/LINALOOL.htm&lt;/div&gt;</summary>
		<author><name>Jy405</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It:Linalool&amp;diff=5024</id>
		<title>It:Linalool</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It:Linalool&amp;diff=5024"/>
		<updated>2006-11-08T15:13:27Z</updated>

		<summary type="html">&lt;p&gt;Jy405: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;==Introduction==&lt;br /&gt;
Lavender is a shrubby plant in the mint family with about 25-30 species. It is native from the Mediterranean region south to tropical Afric and the east to India. The aromatic smell is found in all parts of the shrub, but the essential oil is only produced from the flowers and flower-stalks. The lavender flower oil is a complex mixture compounds containing linalool, linalyl acetate, 1, 8-cineole, β-ocimene and so on.&lt;br /&gt;
&lt;br /&gt;
[[Image:Lavender.jpg]]&lt;br /&gt;
&lt;br /&gt;
A picture of Lavender flower.&lt;br /&gt;
&lt;br /&gt;
==Linalool==&lt;br /&gt;
Linalool is a colourless fragrant liquid which can be found in many essential oil. As a fragrance, it is used in many soaps, detergents, creams, lotions, shampoos and it is a chemical intermediate in the formation of Vitamin E. It is also an insecticide which is safe to humans. &lt;br /&gt;
&lt;br /&gt;
[[Image:2D-structure_of_Linalool.gif]] &lt;br /&gt;
2D-strcture of a Linalool Molecule&lt;br /&gt;
&lt;br /&gt;
&amp;lt;jmol&amp;gt;&lt;br /&gt;
&amp;lt;jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;size&amp;gt;300&amp;lt;/size&amp;gt;&lt;br /&gt;
&amp;lt;color&amp;gt;silver&amp;lt;/color&amp;gt;&lt;br /&gt;
&amp;lt;script&amp;gt;zoom 120; cpk off;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;HEADER    NONAME 06-Nov-06                                              NONE   1&lt;br /&gt;
TITLE                                                                   NONE   2&lt;br /&gt;
AUTHOR    WWW daemon apache                                             NONE   3&lt;br /&gt;
REVDAT   1  06-Nov-06     0                                             NONE   4&lt;br /&gt;
ATOM      1  C           0      -3.030   1.372   0.117  0.00  0.00           C+0&lt;br /&gt;
ATOM      2  C           0      -3.012  -0.132   0.023  0.00  0.00           C+0&lt;br /&gt;
ATOM      3  C           0      -1.921  -0.752  -0.353  0.00  0.00           C+0&lt;br /&gt;
ATOM      4  C           0      -0.650   0.027  -0.573  0.00  0.00           C+0&lt;br /&gt;
ATOM      5  C           0       0.473  -0.580   0.272  0.00  0.00           C+0&lt;br /&gt;
ATOM      6  C           0       1.763   0.211   0.049  0.00  0.00           C+0&lt;br /&gt;
ATOM      7  C           0       1.546   1.668   0.460  0.00  0.00           C+0&lt;br /&gt;
ATOM      8  C           0       2.869  -0.387   0.880  0.00  0.00           C+0&lt;br /&gt;
ATOM      9  C           0       3.947  -0.853   0.300  0.00  0.00           C+0&lt;br /&gt;
ATOM     10  O           0       2.123   0.155  -1.333  0.00  0.00           O+0&lt;br /&gt;
ATOM     11  C           0      -4.249  -0.923   0.362  0.00  0.00           C+0&lt;br /&gt;
ATOM     12  H           0      -2.720   1.799  -0.837  0.00  0.00           H+0&lt;br /&gt;
ATOM     13  H           0      -4.039   1.709   0.356  0.00  0.00           H+0&lt;br /&gt;
ATOM     14  H           0      -2.344   1.695   0.900  0.00  0.00           H+0&lt;br /&gt;
ATOM     15  H           0      -1.932  -1.821  -0.506  0.00  0.00           H+0&lt;br /&gt;
ATOM     16  H           0      -0.375  -0.016  -1.627  0.00  0.00           H+0&lt;br /&gt;
ATOM     17  H           0      -0.804   1.065  -0.279  0.00  0.00           H+0&lt;br /&gt;
ATOM     18  H           0       0.198  -0.537   1.326  0.00  0.00           H+0&lt;br /&gt;
ATOM     19  H           0       0.627  -1.618  -0.022  0.00  0.00           H+0&lt;br /&gt;
ATOM     20  H           0       1.272   1.711   1.514  0.00  0.00           H+0&lt;br /&gt;
ATOM     21  H           0       2.466   2.232   0.301  0.00  0.00           H+0&lt;br /&gt;
ATOM     22  H           0       0.747   2.101  -0.141  0.00  0.00           H+0&lt;br /&gt;
ATOM     23  H           0       2.772  -0.431   1.955  0.00  0.00           H+0&lt;br /&gt;
ATOM     24  H           0       4.739  -1.281   0.896  0.00  0.00           H+0&lt;br /&gt;
ATOM     25  H           0       4.043  -0.809  -0.775  0.00  0.00           H+0&lt;br /&gt;
ATOM     26  H           0       2.251  -0.779  -1.551  0.00  0.00           H+0&lt;br /&gt;
ATOM     27  H           0      -4.046  -1.987   0.237  0.00  0.00           H+0&lt;br /&gt;
ATOM     28  H           0      -4.534  -0.727   1.396  0.00  0.00           H+0&lt;br /&gt;
ATOM     29  H           0      -5.062  -0.628  -0.301  0.00  0.00           H+0&lt;br /&gt;
CONECT    1    2   12   13   14                                         NONE  34&lt;br /&gt;
CONECT    2    1    3   11    0                                         NONE  35&lt;br /&gt;
CONECT    3    2    4   15    0                                         NONE  36&lt;br /&gt;
CONECT    4    3    5   16   17                                         NONE  37&lt;br /&gt;
CONECT    5    4    6   18   19                                         NONE  38&lt;br /&gt;
CONECT    6    5    7    8   10                                         NONE  39&lt;br /&gt;
CONECT    7    6   20   21   22                                         NONE  40&lt;br /&gt;
CONECT    8    6    9   23    0                                         NONE  41&lt;br /&gt;
CONECT    9    8   24   25    0                                         NONE  42&lt;br /&gt;
CONECT   10    6   26    0    0                                         NONE  43&lt;br /&gt;
CONECT   11    2   27   28   29                                         NONE  44&lt;br /&gt;
END                                                                     NONE  45&lt;br /&gt;
&amp;lt;/inlineContents&amp;gt;&lt;br /&gt;
&amp;lt;/jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;/jmol&amp;gt;&lt;br /&gt;
3D -Structure of A Linalool Molecule&lt;br /&gt;
&lt;br /&gt;
{| border=&amp;quot;1&amp;quot;&lt;br /&gt;
|+ The table&#039;s caption&lt;br /&gt;
!  !!&lt;br /&gt;
|-&lt;br /&gt;
! Einecs Number&lt;br /&gt;
| 201-134-4 ||&lt;br /&gt;
|-&lt;br /&gt;
! CAS Number&lt;br /&gt;
|78-70-6 ||&lt;br /&gt;
|-&lt;br /&gt;
! Chemical Name&lt;br /&gt;
|Linalool ||&lt;br /&gt;
|-&lt;br /&gt;
! Autoname&lt;br /&gt;
|3,7-Dimethyl-1,6-octadien-3-ol ||&lt;br /&gt;
|-&lt;br /&gt;
! Molecular Formula&lt;br /&gt;
|C10H18O||&lt;br /&gt;
|-&lt;br /&gt;
! Molecular Weight&lt;br /&gt;
|154.25 g/mol||&lt;br /&gt;
|-&lt;br /&gt;
! Physical State&lt;br /&gt;
|Clear to slightly yellow liquid||&lt;br /&gt;
|-&lt;br /&gt;
! Boiling Point&lt;br /&gt;
|198-200C||&lt;br /&gt;
|-&lt;br /&gt;
! Solubility in Water&lt;br /&gt;
|Insoluble||&lt;br /&gt;
|-&lt;br /&gt;
! Flash Point&lt;br /&gt;
|75C||&lt;br /&gt;
|-&lt;br /&gt;
! Toxicity&lt;br /&gt;
|Oral rat LD50: 2790 mg/kg||&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
==Synthesis of linalool==&lt;br /&gt;
Linalool is an anyclic alcohol. It has a sweet, pleasant fragrance and is one of the most frequently encountered floral scent compounds. Linalool has two enantiomeric forms (R) - linalool and (S) - linalool corresponds to the chiral properties of its hydroxylated third carbon. Traditionally, linalool was obtained from α- or β-pinene. The most modern synthesis start with 2-methyl-2-hepten-6-one and proceed via base-calalyzed ethynylation with acetylene to dehydrolinalool, yielding linalool through hydrogenation of the triple bond in the presence of a palladium-carbon catalyst.&lt;br /&gt;
&lt;br /&gt;
[[Image:Synthesis_of_Linalool_Molecule.gif]]&lt;br /&gt;
&lt;br /&gt;
The process of sysnthesising a linalool molecule.&lt;br /&gt;
&lt;br /&gt;
==Uses of Lavender oil==&lt;br /&gt;
Generally its modern use is for aromatherapy. The research in lab showed that it helped in the reduction of advanced  mammory tumors in lab rats. Some other researches such as potential breast, ovarian, pancreatic, liver, and prostate cancer treatments are on-going.&lt;br /&gt;
Some advocates of alternative medicine claim that lavender oil can be used in a variety of variety.&lt;br /&gt;
 •	Cream: Add a few drops of oil to chamomile cream for eczema.&lt;br /&gt;
 •	Lotion: Add a few drops of oil to a little water for sunburn or scalds.&lt;br /&gt;
 •	Chest Rub: Add 1 ml oil and 5 drops chamomile oil to 10 ml carrier oil for asthmatic and bronchitic spasm.&lt;br /&gt;
 •	Hair Rinse: Dilute 5-10 drops of oil in water for lice, or use a few drops of neat oil on a fine comb for nits.&lt;br /&gt;
 •	Oil Apply undiluted to insect bites and stings: Dilute 10 drops oil in 25 ml carrier oil for sunstroke or to help prevent sunburn. &lt;br /&gt;
 •	Massage Oil: Dilute 1 ml &#039;lavender oil&#039; in 25 ml carrier oil, and massage into painful muscles.Dilute 10 drops in 25 ml carrier oil and massage into the temples and nape of the neck for tension headaches or at the first hint of a migraine.&lt;br /&gt;
&lt;br /&gt;
==Side Effects of Lavender oil==&lt;br /&gt;
A July 1, 2006 article in Science News stated that lavender oil had been implicated in abnormal development of the breasts in young boys.  Boys and girls are particularly sensitive to estrogenic and androgenic compounds because their sex hormone levels are low prior to puberty.There are identified hormonally active compounds in lavender oil which may be contributing to the increase incidence of early breast development in girls and enlarged breasts in boys.&lt;br /&gt;
&lt;br /&gt;
==References==&lt;br /&gt;
1.	http://en.wikipedia.org/wiki/Lavender&lt;br /&gt;
2.	http://www.umich.edu/~chemh215/CHEM216/HonorsCup/hcproposal/251__A.pdf&lt;br /&gt;
3.      http://www.linguasphere.org/dictionary/n-42188-linalool.html&lt;br /&gt;
4.      http://www.chemicalland21.com/specialtychem/perchem/LINALOOL.htm&lt;/div&gt;</summary>
		<author><name>Jy405</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It:Linalool&amp;diff=5023</id>
		<title>It:Linalool</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It:Linalool&amp;diff=5023"/>
		<updated>2006-11-08T14:58:52Z</updated>

		<summary type="html">&lt;p&gt;Jy405: Side effects of lavender oil&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;==Introduction==&lt;br /&gt;
Lavender is a shrubby plant in the mint family with about 25-30 species. It is native from the Mediterranean region south to tropical Afric and the east to India. The aromatic smell is found in all parts of the shrub, but the essential oil is only produced from the flowers and flower-stalks. The lavender flower oil is a complex mixture compounds containing linalool, linalyl acetate, 1, 8-cineole, β-ocimene and so on.&lt;br /&gt;
&lt;br /&gt;
[[Image:Lavender.jpg]]&lt;br /&gt;
&lt;br /&gt;
A picture of Lavender flower.&lt;br /&gt;
&lt;br /&gt;
==Linalool==&lt;br /&gt;
Linalool is a colourless fragrant liquid which can be found in many essential oil. As a fragrance, it is used in many soaps, detergents, creams, lotions, shampoos and it is a chemical intermediate in the formation of Vitamin E. It is also an insecticide which is safe to humans. &lt;br /&gt;
&lt;br /&gt;
[[Image:2D-structure_of_Linalool.gif]] &lt;br /&gt;
2D-strcture of a Linalool Molecule&lt;br /&gt;
&lt;br /&gt;
&amp;lt;jmol&amp;gt;&lt;br /&gt;
&amp;lt;jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;size&amp;gt;300&amp;lt;/size&amp;gt;&lt;br /&gt;
&amp;lt;color&amp;gt;silver&amp;lt;/color&amp;gt;&lt;br /&gt;
&amp;lt;script&amp;gt;zoom 120; cpk off;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;HEADER    NONAME 06-Nov-06                                              NONE   1&lt;br /&gt;
TITLE                                                                   NONE   2&lt;br /&gt;
AUTHOR    WWW daemon apache                                             NONE   3&lt;br /&gt;
REVDAT   1  06-Nov-06     0                                             NONE   4&lt;br /&gt;
ATOM      1  C           0      -3.030   1.372   0.117  0.00  0.00           C+0&lt;br /&gt;
ATOM      2  C           0      -3.012  -0.132   0.023  0.00  0.00           C+0&lt;br /&gt;
ATOM      3  C           0      -1.921  -0.752  -0.353  0.00  0.00           C+0&lt;br /&gt;
ATOM      4  C           0      -0.650   0.027  -0.573  0.00  0.00           C+0&lt;br /&gt;
ATOM      5  C           0       0.473  -0.580   0.272  0.00  0.00           C+0&lt;br /&gt;
ATOM      6  C           0       1.763   0.211   0.049  0.00  0.00           C+0&lt;br /&gt;
ATOM      7  C           0       1.546   1.668   0.460  0.00  0.00           C+0&lt;br /&gt;
ATOM      8  C           0       2.869  -0.387   0.880  0.00  0.00           C+0&lt;br /&gt;
ATOM      9  C           0       3.947  -0.853   0.300  0.00  0.00           C+0&lt;br /&gt;
ATOM     10  O           0       2.123   0.155  -1.333  0.00  0.00           O+0&lt;br /&gt;
ATOM     11  C           0      -4.249  -0.923   0.362  0.00  0.00           C+0&lt;br /&gt;
ATOM     12  H           0      -2.720   1.799  -0.837  0.00  0.00           H+0&lt;br /&gt;
ATOM     13  H           0      -4.039   1.709   0.356  0.00  0.00           H+0&lt;br /&gt;
ATOM     14  H           0      -2.344   1.695   0.900  0.00  0.00           H+0&lt;br /&gt;
ATOM     15  H           0      -1.932  -1.821  -0.506  0.00  0.00           H+0&lt;br /&gt;
ATOM     16  H           0      -0.375  -0.016  -1.627  0.00  0.00           H+0&lt;br /&gt;
ATOM     17  H           0      -0.804   1.065  -0.279  0.00  0.00           H+0&lt;br /&gt;
ATOM     18  H           0       0.198  -0.537   1.326  0.00  0.00           H+0&lt;br /&gt;
ATOM     19  H           0       0.627  -1.618  -0.022  0.00  0.00           H+0&lt;br /&gt;
ATOM     20  H           0       1.272   1.711   1.514  0.00  0.00           H+0&lt;br /&gt;
ATOM     21  H           0       2.466   2.232   0.301  0.00  0.00           H+0&lt;br /&gt;
ATOM     22  H           0       0.747   2.101  -0.141  0.00  0.00           H+0&lt;br /&gt;
ATOM     23  H           0       2.772  -0.431   1.955  0.00  0.00           H+0&lt;br /&gt;
ATOM     24  H           0       4.739  -1.281   0.896  0.00  0.00           H+0&lt;br /&gt;
ATOM     25  H           0       4.043  -0.809  -0.775  0.00  0.00           H+0&lt;br /&gt;
ATOM     26  H           0       2.251  -0.779  -1.551  0.00  0.00           H+0&lt;br /&gt;
ATOM     27  H           0      -4.046  -1.987   0.237  0.00  0.00           H+0&lt;br /&gt;
ATOM     28  H           0      -4.534  -0.727   1.396  0.00  0.00           H+0&lt;br /&gt;
ATOM     29  H           0      -5.062  -0.628  -0.301  0.00  0.00           H+0&lt;br /&gt;
CONECT    1    2   12   13   14                                         NONE  34&lt;br /&gt;
CONECT    2    1    3   11    0                                         NONE  35&lt;br /&gt;
CONECT    3    2    4   15    0                                         NONE  36&lt;br /&gt;
CONECT    4    3    5   16   17                                         NONE  37&lt;br /&gt;
CONECT    5    4    6   18   19                                         NONE  38&lt;br /&gt;
CONECT    6    5    7    8   10                                         NONE  39&lt;br /&gt;
CONECT    7    6   20   21   22                                         NONE  40&lt;br /&gt;
CONECT    8    6    9   23    0                                         NONE  41&lt;br /&gt;
CONECT    9    8   24   25    0                                         NONE  42&lt;br /&gt;
CONECT   10    6   26    0    0                                         NONE  43&lt;br /&gt;
CONECT   11    2   27   28   29                                         NONE  44&lt;br /&gt;
END                                                                     NONE  45&lt;br /&gt;
&amp;lt;/inlineContents&amp;gt;&lt;br /&gt;
&amp;lt;/jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;/jmol&amp;gt;&lt;br /&gt;
3D -Structure of A Linalool Molecule&lt;br /&gt;
&lt;br /&gt;
{| border=&amp;quot;1&amp;quot;&lt;br /&gt;
|+ The table&#039;s caption&lt;br /&gt;
!  !!&lt;br /&gt;
|-&lt;br /&gt;
! Einecs Number&lt;br /&gt;
| 201-134-4 ||&lt;br /&gt;
|-&lt;br /&gt;
! CAS Number&lt;br /&gt;
|78-70-6 ||&lt;br /&gt;
|-&lt;br /&gt;
! Chemical Name&lt;br /&gt;
|Linalool ||&lt;br /&gt;
|-&lt;br /&gt;
! Autoname&lt;br /&gt;
|3,7-Dimethyl-1,6-octadien-3-ol ||&lt;br /&gt;
|-&lt;br /&gt;
! Molecular Formula&lt;br /&gt;
|C10H18O||&lt;br /&gt;
|-&lt;br /&gt;
! Molecular Weight&lt;br /&gt;
|154.25 g/mol||&lt;br /&gt;
|-&lt;br /&gt;
! Physical State&lt;br /&gt;
|Clear to slightly yellow liquid||&lt;br /&gt;
|-&lt;br /&gt;
! Boiling Point&lt;br /&gt;
|198-200C||&lt;br /&gt;
|-&lt;br /&gt;
! Solubility in Water&lt;br /&gt;
|Insoluble||&lt;br /&gt;
|-&lt;br /&gt;
! Flash Point&lt;br /&gt;
|75C||&lt;br /&gt;
|-&lt;br /&gt;
! Toxicity&lt;br /&gt;
|Oral rat LD50: 2790 mg/kg||&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
==Synthesis of linalool==&lt;br /&gt;
Linalool is an anyclic alcohol. It has a sweet, pleasant fragrance and is one of the most frequently encountered floral scent compounds. Linalool has two enantiomeric forms (R) - linalool and (S) - linalool corresponds to the chiral properties of its hydroxylated third carbon. Traditionally, linalool was obtained from α- or β-pinene. The most modern synthesis start with 2-methyl-2-hepten-6-one and proceed via base-calalyzed ethynylation with acetylene to dehydrolinalool, yielding linalool through hydrogenation of the triple bond in the presence of a palladium-carbon catalyst.&lt;br /&gt;
&lt;br /&gt;
[[Image:Synthesis_of_Linalool_Molecule.gif]]&lt;br /&gt;
&lt;br /&gt;
The process of sysnthesising a linalool molecule.&lt;br /&gt;
&lt;br /&gt;
==Uses of Lavender oil==&lt;br /&gt;
Generally its modern use is for aromatherapy. The research in lab showed that it helped in the reduction of advanced  mammory tumors in lab rats. Some other researches such as potential breast, ovarian, pancreatic, liver, and prostate cancer treatments are on-going.&lt;br /&gt;
Some advocates of alternative medicine claim that lavender oil can be used in a variety of variety.&lt;br /&gt;
 •	Cream: Add a few drops of oil to chamomile cream for eczema.&lt;br /&gt;
 •	Lotion: Add a few drops of oil to a little water for sunburn or scalds.&lt;br /&gt;
 •	Chest Rub: Add 1 ml oil and 5 drops chamomile oil to 10 ml carrier oil for asthmatic and bronchitic spasm.&lt;br /&gt;
 •	Hair Rinse: Dilute 5-10 drops of oil in water for lice, or use a few drops of neat oil on a fine comb for nits.&lt;br /&gt;
 •	Oil Apply undiluted to insect bites and stings: Dilute 10 drops oil in 25 ml carrier oil for sunstroke or to help prevent sunburn. &lt;br /&gt;
 •	Massage Oil: Dilute 1 ml &#039;lavender oil&#039; in 25 ml carrier oil, and massage into painful muscles.Dilute 10 drops in 25 ml carrier oil and massage into the temples and nape of the neck for tension headaches or at the first hint of a migraine.&lt;br /&gt;
&lt;br /&gt;
==Side Effects of Lavender oil==&lt;br /&gt;
A July 1, 2006 article in Science News stated that lavender oil had been implicated in abnormal development of the breasts in young boys.  Boys and girls are particularly sensitive to estrogenic and androgenic compounds because their sex hormone levels are low prior to puberty.There are identified hormonally active compounds in lavender oil which may be contributing to the increase incidence of early breast development in girls and enlarged breasts in boys.&lt;/div&gt;</summary>
		<author><name>Jy405</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It:Linalool&amp;diff=4986</id>
		<title>It:Linalool</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It:Linalool&amp;diff=4986"/>
		<updated>2006-11-07T11:40:13Z</updated>

		<summary type="html">&lt;p&gt;Jy405: /* Linalool */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;==Introduction==&lt;br /&gt;
Lavender is a shrubby plant in the mint family with about 25-30 species. It is native from the Mediterranean region south to tropical Afric and the east to India. The aromatic smell is found in all parts of the shrub, but the essential oil is only produced from the flowers and flower-stalks. The lavender flower oil is a complex mixture compounds containing linalool, linalyl acetate, 1, 8-cineole, β-ocimene and so on.&lt;br /&gt;
&lt;br /&gt;
[[Image:Lavender.jpg]]&lt;br /&gt;
&lt;br /&gt;
A picture of Lavender flower.&lt;br /&gt;
&lt;br /&gt;
==Linalool==&lt;br /&gt;
Linalool is a colourless fragrant liquid which can be found in many essential oil. As a fragrance, it is used in many soaps, detergents, creams, lotions, shampoos and it is a chemical intermediate in the formation of Vitamin E. It is also an insecticide which is safe to humans. &lt;br /&gt;
&lt;br /&gt;
[[Image:2D-structure_of_Linalool.gif]] &lt;br /&gt;
2D-strcture of a Linalool Molecule&lt;br /&gt;
&lt;br /&gt;
&amp;lt;jmol&amp;gt;&lt;br /&gt;
&amp;lt;jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;size&amp;gt;300&amp;lt;/size&amp;gt;&lt;br /&gt;
&amp;lt;color&amp;gt;silver&amp;lt;/color&amp;gt;&lt;br /&gt;
&amp;lt;script&amp;gt;zoom 120; cpk off;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;HEADER    NONAME 06-Nov-06                                              NONE   1&lt;br /&gt;
TITLE                                                                   NONE   2&lt;br /&gt;
AUTHOR    WWW daemon apache                                             NONE   3&lt;br /&gt;
REVDAT   1  06-Nov-06     0                                             NONE   4&lt;br /&gt;
ATOM      1  C           0      -3.030   1.372   0.117  0.00  0.00           C+0&lt;br /&gt;
ATOM      2  C           0      -3.012  -0.132   0.023  0.00  0.00           C+0&lt;br /&gt;
ATOM      3  C           0      -1.921  -0.752  -0.353  0.00  0.00           C+0&lt;br /&gt;
ATOM      4  C           0      -0.650   0.027  -0.573  0.00  0.00           C+0&lt;br /&gt;
ATOM      5  C           0       0.473  -0.580   0.272  0.00  0.00           C+0&lt;br /&gt;
ATOM      6  C           0       1.763   0.211   0.049  0.00  0.00           C+0&lt;br /&gt;
ATOM      7  C           0       1.546   1.668   0.460  0.00  0.00           C+0&lt;br /&gt;
ATOM      8  C           0       2.869  -0.387   0.880  0.00  0.00           C+0&lt;br /&gt;
ATOM      9  C           0       3.947  -0.853   0.300  0.00  0.00           C+0&lt;br /&gt;
ATOM     10  O           0       2.123   0.155  -1.333  0.00  0.00           O+0&lt;br /&gt;
ATOM     11  C           0      -4.249  -0.923   0.362  0.00  0.00           C+0&lt;br /&gt;
ATOM     12  H           0      -2.720   1.799  -0.837  0.00  0.00           H+0&lt;br /&gt;
ATOM     13  H           0      -4.039   1.709   0.356  0.00  0.00           H+0&lt;br /&gt;
ATOM     14  H           0      -2.344   1.695   0.900  0.00  0.00           H+0&lt;br /&gt;
ATOM     15  H           0      -1.932  -1.821  -0.506  0.00  0.00           H+0&lt;br /&gt;
ATOM     16  H           0      -0.375  -0.016  -1.627  0.00  0.00           H+0&lt;br /&gt;
ATOM     17  H           0      -0.804   1.065  -0.279  0.00  0.00           H+0&lt;br /&gt;
ATOM     18  H           0       0.198  -0.537   1.326  0.00  0.00           H+0&lt;br /&gt;
ATOM     19  H           0       0.627  -1.618  -0.022  0.00  0.00           H+0&lt;br /&gt;
ATOM     20  H           0       1.272   1.711   1.514  0.00  0.00           H+0&lt;br /&gt;
ATOM     21  H           0       2.466   2.232   0.301  0.00  0.00           H+0&lt;br /&gt;
ATOM     22  H           0       0.747   2.101  -0.141  0.00  0.00           H+0&lt;br /&gt;
ATOM     23  H           0       2.772  -0.431   1.955  0.00  0.00           H+0&lt;br /&gt;
ATOM     24  H           0       4.739  -1.281   0.896  0.00  0.00           H+0&lt;br /&gt;
ATOM     25  H           0       4.043  -0.809  -0.775  0.00  0.00           H+0&lt;br /&gt;
ATOM     26  H           0       2.251  -0.779  -1.551  0.00  0.00           H+0&lt;br /&gt;
ATOM     27  H           0      -4.046  -1.987   0.237  0.00  0.00           H+0&lt;br /&gt;
ATOM     28  H           0      -4.534  -0.727   1.396  0.00  0.00           H+0&lt;br /&gt;
ATOM     29  H           0      -5.062  -0.628  -0.301  0.00  0.00           H+0&lt;br /&gt;
CONECT    1    2   12   13   14                                         NONE  34&lt;br /&gt;
CONECT    2    1    3   11    0                                         NONE  35&lt;br /&gt;
CONECT    3    2    4   15    0                                         NONE  36&lt;br /&gt;
CONECT    4    3    5   16   17                                         NONE  37&lt;br /&gt;
CONECT    5    4    6   18   19                                         NONE  38&lt;br /&gt;
CONECT    6    5    7    8   10                                         NONE  39&lt;br /&gt;
CONECT    7    6   20   21   22                                         NONE  40&lt;br /&gt;
CONECT    8    6    9   23    0                                         NONE  41&lt;br /&gt;
CONECT    9    8   24   25    0                                         NONE  42&lt;br /&gt;
CONECT   10    6   26    0    0                                         NONE  43&lt;br /&gt;
CONECT   11    2   27   28   29                                         NONE  44&lt;br /&gt;
END                                                                     NONE  45&lt;br /&gt;
&amp;lt;/inlineContents&amp;gt;&lt;br /&gt;
&amp;lt;/jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;/jmol&amp;gt;&lt;br /&gt;
3D -Structure of A Linalool Molecule&lt;br /&gt;
&lt;br /&gt;
{| border=&amp;quot;1&amp;quot;&lt;br /&gt;
|+ The table&#039;s caption&lt;br /&gt;
!  !!&lt;br /&gt;
|-&lt;br /&gt;
! Einecs Number&lt;br /&gt;
| 201-134-4 ||&lt;br /&gt;
|-&lt;br /&gt;
! CAS Number&lt;br /&gt;
|78-70-6 ||&lt;br /&gt;
|-&lt;br /&gt;
! Chemical Name&lt;br /&gt;
|Linalool ||&lt;br /&gt;
|-&lt;br /&gt;
! Autoname&lt;br /&gt;
|3,7-Dimethyl-1,6-octadien-3-ol ||&lt;br /&gt;
|-&lt;br /&gt;
! Molecular Formula&lt;br /&gt;
|C10H18O||&lt;br /&gt;
|-&lt;br /&gt;
! Molecular Weight&lt;br /&gt;
|154.25 g/mol||&lt;br /&gt;
|-&lt;br /&gt;
! Physical State&lt;br /&gt;
|Clear to slightly yellow liquid||&lt;br /&gt;
|-&lt;br /&gt;
! Boiling Point&lt;br /&gt;
|198-200C||&lt;br /&gt;
|-&lt;br /&gt;
! Solubility in Water&lt;br /&gt;
|Insoluble||&lt;br /&gt;
|-&lt;br /&gt;
! Flash Point&lt;br /&gt;
|75C||&lt;br /&gt;
|-&lt;br /&gt;
! Toxicity&lt;br /&gt;
|Oral rat LD50: 2790 mg/kg||&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
==Synthesis of linalool==&lt;br /&gt;
Linalool is an anyclic alcohol. It has a sweet, pleasant fragrance and is one of the most frequently encountered floral scent compounds. Linalool has two enantiomeric forms (R) - linalool and (S) - linalool corresponds to the chiral properties of its hydroxylated third carbon. Traditionally, linalool was obtained from α- or β-pinene. The most modern synthesis start with 2-methyl-2-hepten-6-one and proceed via base-calalyzed ethynylation with acetylene to dehydrolinalool, yielding linalool through hydrogenation of the triple bond in the presence of a palladium-carbon catalyst.&lt;br /&gt;
&lt;br /&gt;
[[Image:Synthesis_of_Linalool_Molecule.gif]]&lt;br /&gt;
&lt;br /&gt;
The process of sysnthesising a linalool molecule.&lt;br /&gt;
&lt;br /&gt;
==Uses of Lavender oil==&lt;br /&gt;
Generally its modern use is for aromatherapy. The research in lab showed that it helped in the reduction of advanced  mammory tumors in lab rats. Some other researches such as potential breast, ovarian, pancreatic, liver, and prostate cancer treatments are on-going.&lt;br /&gt;
Some advocates of alternative medicine claim that lavender oil can be used in a variety of variety.&lt;br /&gt;
 •	Cream: Add a few drops of oil to chamomile cream for eczema.&lt;br /&gt;
 •	Lotion: Add a few drops of oil to a little water for sunburn or scalds.&lt;br /&gt;
 •	Chest Rub: Add 1 ml oil and 5 drops chamomile oil to 10 ml carrier oil for asthmatic and bronchitic spasm.&lt;br /&gt;
 •	Hair Rinse: Dilute 5-10 drops of oil in water for lice, or use a few drops of neat oil on a fine comb for nits.&lt;br /&gt;
 •	Oil Apply undiluted to insect bites and stings: Dilute 10 drops oil in 25 ml carrier oil for sunstroke or to help prevent sunburn. &lt;br /&gt;
 •	Massage Oil: Dilute 1 ml &#039;lavender oil&#039; in 25 ml carrier oil, and massage into painful muscles.Dilute 10 drops in 25 ml carrier oil and massage into the temples and nape of the neck for tension headaches or at the first hint of a migraine.&lt;/div&gt;</summary>
		<author><name>Jy405</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It:Linalool&amp;diff=4983</id>
		<title>It:Linalool</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It:Linalool&amp;diff=4983"/>
		<updated>2006-11-07T11:33:49Z</updated>

		<summary type="html">&lt;p&gt;Jy405: /* Synthesis of linalool */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;==Introduction==&lt;br /&gt;
Lavender is a shrubby plant in the mint family with about 25-30 species. It is native from the Mediterranean region south to tropical Afric and the east to India. The aromatic smell is found in all parts of the shrub, but the essential oil is only produced from the flowers and flower-stalks. The lavender flower oil is a complex mixture compounds containing linalool, linalyl acetate, 1, 8-cineole, β-ocimene and so on.&lt;br /&gt;
&lt;br /&gt;
[[Image:Lavender.jpg]]&lt;br /&gt;
&lt;br /&gt;
A picture of Lavender flower.&lt;br /&gt;
&lt;br /&gt;
==Linalool==&lt;br /&gt;
Linalool is a colourless fragrant liquid which can be found in many essential oil.&lt;br /&gt;
&lt;br /&gt;
[[Image:2D-structure_of_Linalool.gif]] &lt;br /&gt;
2D-strcture of a Linalool Molecule&lt;br /&gt;
&lt;br /&gt;
&amp;lt;jmol&amp;gt;&lt;br /&gt;
&amp;lt;jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;size&amp;gt;300&amp;lt;/size&amp;gt;&lt;br /&gt;
&amp;lt;color&amp;gt;silver&amp;lt;/color&amp;gt;&lt;br /&gt;
&amp;lt;script&amp;gt;zoom 120; cpk off;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;HEADER    NONAME 06-Nov-06                                              NONE   1&lt;br /&gt;
TITLE                                                                   NONE   2&lt;br /&gt;
AUTHOR    WWW daemon apache                                             NONE   3&lt;br /&gt;
REVDAT   1  06-Nov-06     0                                             NONE   4&lt;br /&gt;
ATOM      1  C           0      -3.030   1.372   0.117  0.00  0.00           C+0&lt;br /&gt;
ATOM      2  C           0      -3.012  -0.132   0.023  0.00  0.00           C+0&lt;br /&gt;
ATOM      3  C           0      -1.921  -0.752  -0.353  0.00  0.00           C+0&lt;br /&gt;
ATOM      4  C           0      -0.650   0.027  -0.573  0.00  0.00           C+0&lt;br /&gt;
ATOM      5  C           0       0.473  -0.580   0.272  0.00  0.00           C+0&lt;br /&gt;
ATOM      6  C           0       1.763   0.211   0.049  0.00  0.00           C+0&lt;br /&gt;
ATOM      7  C           0       1.546   1.668   0.460  0.00  0.00           C+0&lt;br /&gt;
ATOM      8  C           0       2.869  -0.387   0.880  0.00  0.00           C+0&lt;br /&gt;
ATOM      9  C           0       3.947  -0.853   0.300  0.00  0.00           C+0&lt;br /&gt;
ATOM     10  O           0       2.123   0.155  -1.333  0.00  0.00           O+0&lt;br /&gt;
ATOM     11  C           0      -4.249  -0.923   0.362  0.00  0.00           C+0&lt;br /&gt;
ATOM     12  H           0      -2.720   1.799  -0.837  0.00  0.00           H+0&lt;br /&gt;
ATOM     13  H           0      -4.039   1.709   0.356  0.00  0.00           H+0&lt;br /&gt;
ATOM     14  H           0      -2.344   1.695   0.900  0.00  0.00           H+0&lt;br /&gt;
ATOM     15  H           0      -1.932  -1.821  -0.506  0.00  0.00           H+0&lt;br /&gt;
ATOM     16  H           0      -0.375  -0.016  -1.627  0.00  0.00           H+0&lt;br /&gt;
ATOM     17  H           0      -0.804   1.065  -0.279  0.00  0.00           H+0&lt;br /&gt;
ATOM     18  H           0       0.198  -0.537   1.326  0.00  0.00           H+0&lt;br /&gt;
ATOM     19  H           0       0.627  -1.618  -0.022  0.00  0.00           H+0&lt;br /&gt;
ATOM     20  H           0       1.272   1.711   1.514  0.00  0.00           H+0&lt;br /&gt;
ATOM     21  H           0       2.466   2.232   0.301  0.00  0.00           H+0&lt;br /&gt;
ATOM     22  H           0       0.747   2.101  -0.141  0.00  0.00           H+0&lt;br /&gt;
ATOM     23  H           0       2.772  -0.431   1.955  0.00  0.00           H+0&lt;br /&gt;
ATOM     24  H           0       4.739  -1.281   0.896  0.00  0.00           H+0&lt;br /&gt;
ATOM     25  H           0       4.043  -0.809  -0.775  0.00  0.00           H+0&lt;br /&gt;
ATOM     26  H           0       2.251  -0.779  -1.551  0.00  0.00           H+0&lt;br /&gt;
ATOM     27  H           0      -4.046  -1.987   0.237  0.00  0.00           H+0&lt;br /&gt;
ATOM     28  H           0      -4.534  -0.727   1.396  0.00  0.00           H+0&lt;br /&gt;
ATOM     29  H           0      -5.062  -0.628  -0.301  0.00  0.00           H+0&lt;br /&gt;
CONECT    1    2   12   13   14                                         NONE  34&lt;br /&gt;
CONECT    2    1    3   11    0                                         NONE  35&lt;br /&gt;
CONECT    3    2    4   15    0                                         NONE  36&lt;br /&gt;
CONECT    4    3    5   16   17                                         NONE  37&lt;br /&gt;
CONECT    5    4    6   18   19                                         NONE  38&lt;br /&gt;
CONECT    6    5    7    8   10                                         NONE  39&lt;br /&gt;
CONECT    7    6   20   21   22                                         NONE  40&lt;br /&gt;
CONECT    8    6    9   23    0                                         NONE  41&lt;br /&gt;
CONECT    9    8   24   25    0                                         NONE  42&lt;br /&gt;
CONECT   10    6   26    0    0                                         NONE  43&lt;br /&gt;
CONECT   11    2   27   28   29                                         NONE  44&lt;br /&gt;
END                                                                     NONE  45&lt;br /&gt;
&amp;lt;/inlineContents&amp;gt;&lt;br /&gt;
&amp;lt;/jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;/jmol&amp;gt;&lt;br /&gt;
3D -Structure of A Linalool Molecule&lt;br /&gt;
&lt;br /&gt;
{| border=&amp;quot;1&amp;quot;&lt;br /&gt;
|+ The table&#039;s caption&lt;br /&gt;
!  !!&lt;br /&gt;
|-&lt;br /&gt;
! Einecs Number&lt;br /&gt;
| 201-134-4 ||&lt;br /&gt;
|-&lt;br /&gt;
! CAS Number&lt;br /&gt;
|78-70-6 ||&lt;br /&gt;
|-&lt;br /&gt;
! Chemical Name&lt;br /&gt;
|Linalool ||&lt;br /&gt;
|-&lt;br /&gt;
! Autoname&lt;br /&gt;
|3,7-Dimethyl-1,6-octadien-3-ol ||&lt;br /&gt;
|-&lt;br /&gt;
! Molecular Formula&lt;br /&gt;
|C10H18O||&lt;br /&gt;
|-&lt;br /&gt;
! Molecular Weight&lt;br /&gt;
|154.25 g/mol||&lt;br /&gt;
|-&lt;br /&gt;
! Physical State&lt;br /&gt;
|Clear to slightly yellow liquid||&lt;br /&gt;
|-&lt;br /&gt;
! Boiling Point&lt;br /&gt;
|198-200C||&lt;br /&gt;
|-&lt;br /&gt;
! Solubility in Water&lt;br /&gt;
|Insoluble||&lt;br /&gt;
|-&lt;br /&gt;
! Flash Point&lt;br /&gt;
|75C||&lt;br /&gt;
|-&lt;br /&gt;
! Toxicity&lt;br /&gt;
|Oral rat LD50: 2790 mg/kg||&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
==Synthesis of linalool==&lt;br /&gt;
Linalool is an anyclic alcohol. It has a sweet, pleasant fragrance and is one of the most frequently encountered floral scent compounds. Linalool has two enantiomeric forms (R) - linalool and (S) - linalool corresponds to the chiral properties of its hydroxylated third carbon. Traditionally, linalool was obtained from α- or β-pinene. The most modern synthesis start with 2-methyl-2-hepten-6-one and proceed via base-calalyzed ethynylation with acetylene to dehydrolinalool, yielding linalool through hydrogenation of the triple bond in the presence of a palladium-carbon catalyst.&lt;br /&gt;
&lt;br /&gt;
[[Image:Synthesis_of_Linalool_Molecule.gif]]&lt;br /&gt;
&lt;br /&gt;
The process of sysnthesising a linalool molecule.&lt;br /&gt;
&lt;br /&gt;
==Uses of Lavender oil==&lt;br /&gt;
Generally its modern use is for aromatherapy. The research in lab showed that it helped in the reduction of advanced  mammory tumors in lab rats. Some other researches such as potential breast, ovarian, pancreatic, liver, and prostate cancer treatments are on-going.&lt;br /&gt;
Some advocates of alternative medicine claim that lavender oil can be used in a variety of variety.&lt;br /&gt;
 •	Cream: Add a few drops of oil to chamomile cream for eczema.&lt;br /&gt;
 •	Lotion: Add a few drops of oil to a little water for sunburn or scalds.&lt;br /&gt;
 •	Chest Rub: Add 1 ml oil and 5 drops chamomile oil to 10 ml carrier oil for asthmatic and bronchitic spasm.&lt;br /&gt;
 •	Hair Rinse: Dilute 5-10 drops of oil in water for lice, or use a few drops of neat oil on a fine comb for nits.&lt;br /&gt;
 •	Oil Apply undiluted to insect bites and stings: Dilute 10 drops oil in 25 ml carrier oil for sunstroke or to help prevent sunburn. &lt;br /&gt;
 •	Massage Oil: Dilute 1 ml &#039;lavender oil&#039; in 25 ml carrier oil, and massage into painful muscles.Dilute 10 drops in 25 ml carrier oil and massage into the temples and nape of the neck for tension headaches or at the first hint of a migraine.&lt;/div&gt;</summary>
		<author><name>Jy405</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It:Linalool&amp;diff=4960</id>
		<title>It:Linalool</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It:Linalool&amp;diff=4960"/>
		<updated>2006-11-06T16:27:57Z</updated>

		<summary type="html">&lt;p&gt;Jy405: 3D-structure of a Linalool molecule&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;==Introduction==&lt;br /&gt;
Lavender is a shrubby plant in the mint family with about 25-30 species. It is native from the Mediterranean region south to tropical Afric and the east to India. The aromatic smell is found in all parts of the shrub, but the essential oil is only produced from the flowers and flower-stalks. The lavender flower oil is a complex mixture compounds containing linalool, linalyl acetate, 1, 8-cineole, β-ocimene and so on.&lt;br /&gt;
&lt;br /&gt;
[[Image:Lavender.jpg]]&lt;br /&gt;
&lt;br /&gt;
A picture of Lavender flower.&lt;br /&gt;
&lt;br /&gt;
==Linalool==&lt;br /&gt;
Linalool is a colourless fragrant liquid which can be found in many essential oil.&lt;br /&gt;
&lt;br /&gt;
[[Image:2D-structure_of_Linalool.gif]] &lt;br /&gt;
2D-strcture of a Linalool Molecule&lt;br /&gt;
&lt;br /&gt;
&amp;lt;jmol&amp;gt;&lt;br /&gt;
&amp;lt;jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;size&amp;gt;300&amp;lt;/size&amp;gt;&lt;br /&gt;
&amp;lt;color&amp;gt;silver&amp;lt;/color&amp;gt;&lt;br /&gt;
&amp;lt;script&amp;gt;zoom 120; cpk off;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;HEADER    NONAME 06-Nov-06                                              NONE   1&lt;br /&gt;
TITLE                                                                   NONE   2&lt;br /&gt;
AUTHOR    WWW daemon apache                                             NONE   3&lt;br /&gt;
REVDAT   1  06-Nov-06     0                                             NONE   4&lt;br /&gt;
ATOM      1  C           0      -3.030   1.372   0.117  0.00  0.00           C+0&lt;br /&gt;
ATOM      2  C           0      -3.012  -0.132   0.023  0.00  0.00           C+0&lt;br /&gt;
ATOM      3  C           0      -1.921  -0.752  -0.353  0.00  0.00           C+0&lt;br /&gt;
ATOM      4  C           0      -0.650   0.027  -0.573  0.00  0.00           C+0&lt;br /&gt;
ATOM      5  C           0       0.473  -0.580   0.272  0.00  0.00           C+0&lt;br /&gt;
ATOM      6  C           0       1.763   0.211   0.049  0.00  0.00           C+0&lt;br /&gt;
ATOM      7  C           0       1.546   1.668   0.460  0.00  0.00           C+0&lt;br /&gt;
ATOM      8  C           0       2.869  -0.387   0.880  0.00  0.00           C+0&lt;br /&gt;
ATOM      9  C           0       3.947  -0.853   0.300  0.00  0.00           C+0&lt;br /&gt;
ATOM     10  O           0       2.123   0.155  -1.333  0.00  0.00           O+0&lt;br /&gt;
ATOM     11  C           0      -4.249  -0.923   0.362  0.00  0.00           C+0&lt;br /&gt;
ATOM     12  H           0      -2.720   1.799  -0.837  0.00  0.00           H+0&lt;br /&gt;
ATOM     13  H           0      -4.039   1.709   0.356  0.00  0.00           H+0&lt;br /&gt;
ATOM     14  H           0      -2.344   1.695   0.900  0.00  0.00           H+0&lt;br /&gt;
ATOM     15  H           0      -1.932  -1.821  -0.506  0.00  0.00           H+0&lt;br /&gt;
ATOM     16  H           0      -0.375  -0.016  -1.627  0.00  0.00           H+0&lt;br /&gt;
ATOM     17  H           0      -0.804   1.065  -0.279  0.00  0.00           H+0&lt;br /&gt;
ATOM     18  H           0       0.198  -0.537   1.326  0.00  0.00           H+0&lt;br /&gt;
ATOM     19  H           0       0.627  -1.618  -0.022  0.00  0.00           H+0&lt;br /&gt;
ATOM     20  H           0       1.272   1.711   1.514  0.00  0.00           H+0&lt;br /&gt;
ATOM     21  H           0       2.466   2.232   0.301  0.00  0.00           H+0&lt;br /&gt;
ATOM     22  H           0       0.747   2.101  -0.141  0.00  0.00           H+0&lt;br /&gt;
ATOM     23  H           0       2.772  -0.431   1.955  0.00  0.00           H+0&lt;br /&gt;
ATOM     24  H           0       4.739  -1.281   0.896  0.00  0.00           H+0&lt;br /&gt;
ATOM     25  H           0       4.043  -0.809  -0.775  0.00  0.00           H+0&lt;br /&gt;
ATOM     26  H           0       2.251  -0.779  -1.551  0.00  0.00           H+0&lt;br /&gt;
ATOM     27  H           0      -4.046  -1.987   0.237  0.00  0.00           H+0&lt;br /&gt;
ATOM     28  H           0      -4.534  -0.727   1.396  0.00  0.00           H+0&lt;br /&gt;
ATOM     29  H           0      -5.062  -0.628  -0.301  0.00  0.00           H+0&lt;br /&gt;
CONECT    1    2   12   13   14                                         NONE  34&lt;br /&gt;
CONECT    2    1    3   11    0                                         NONE  35&lt;br /&gt;
CONECT    3    2    4   15    0                                         NONE  36&lt;br /&gt;
CONECT    4    3    5   16   17                                         NONE  37&lt;br /&gt;
CONECT    5    4    6   18   19                                         NONE  38&lt;br /&gt;
CONECT    6    5    7    8   10                                         NONE  39&lt;br /&gt;
CONECT    7    6   20   21   22                                         NONE  40&lt;br /&gt;
CONECT    8    6    9   23    0                                         NONE  41&lt;br /&gt;
CONECT    9    8   24   25    0                                         NONE  42&lt;br /&gt;
CONECT   10    6   26    0    0                                         NONE  43&lt;br /&gt;
CONECT   11    2   27   28   29                                         NONE  44&lt;br /&gt;
END                                                                     NONE  45&lt;br /&gt;
&amp;lt;/inlineContents&amp;gt;&lt;br /&gt;
&amp;lt;/jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;/jmol&amp;gt;&lt;br /&gt;
3D -Structure of A Linalool Molecule&lt;br /&gt;
&lt;br /&gt;
{| border=&amp;quot;1&amp;quot;&lt;br /&gt;
|+ The table&#039;s caption&lt;br /&gt;
!  !!&lt;br /&gt;
|-&lt;br /&gt;
! Einecs Number&lt;br /&gt;
| 201-134-4 ||&lt;br /&gt;
|-&lt;br /&gt;
! CAS Number&lt;br /&gt;
|78-70-6 ||&lt;br /&gt;
|-&lt;br /&gt;
! Chemical Name&lt;br /&gt;
|Linalool ||&lt;br /&gt;
|-&lt;br /&gt;
! Autoname&lt;br /&gt;
|3,7-Dimethyl-1,6-octadien-3-ol ||&lt;br /&gt;
|-&lt;br /&gt;
! Molecular Formula&lt;br /&gt;
|C10H18O||&lt;br /&gt;
|-&lt;br /&gt;
! Molecular Weight&lt;br /&gt;
|154.25 g/mol||&lt;br /&gt;
|-&lt;br /&gt;
! Physical State&lt;br /&gt;
|Clear to slightly yellow liquid||&lt;br /&gt;
|-&lt;br /&gt;
! Boiling Point&lt;br /&gt;
|198-200C||&lt;br /&gt;
|-&lt;br /&gt;
! Solubility in Water&lt;br /&gt;
|Insoluble||&lt;br /&gt;
|-&lt;br /&gt;
! Flash Point&lt;br /&gt;
|75C||&lt;br /&gt;
|-&lt;br /&gt;
! Toxicity&lt;br /&gt;
|Oral rat LD50: 2790 mg/kg||&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
==Synthesis of linalool==&lt;br /&gt;
Linalool is an anyclic alcohol. It has a sweet, pleasant fragrance and is one of the most frequently encountered floral scent compounds. Linalool has two enantiomeric forms (R) - linalool and (S) - linalool corresponds to the chiral properties of its hydroxylated third carbon. Traditionally, linalool was obtained from α- or β-pinene. The most modern synthesis start with 2-methyl-2-hepten-6-one and proceed via base-calalyzed ethynylation with acetylene to dehydrolinalool, yielding linalool through hydrogenation of the triple bond in the presence of a palladium-carbon catalyst.&lt;br /&gt;
&lt;br /&gt;
[[Image:Synthesis_of_Linalool_Molecule.gif]]&lt;br /&gt;
&lt;br /&gt;
The process of sysnthesising linalool molecule using 3,7-dimethyl-1,6-octadien-3-ol.&lt;br /&gt;
&lt;br /&gt;
==Uses of Lavender oil==&lt;br /&gt;
Generally its modern use is for aromatherapy. The research in lab showed that it helped in the reduction of advanced  mammory tumors in lab rats. Some other researches such as potential breast, ovarian, pancreatic, liver, and prostate cancer treatments are on-going.&lt;br /&gt;
Some advocates of alternative medicine claim that lavender oil can be used in a variety of variety.&lt;br /&gt;
 •	Cream: Add a few drops of oil to chamomile cream for eczema.&lt;br /&gt;
 •	Lotion: Add a few drops of oil to a little water for sunburn or scalds.&lt;br /&gt;
 •	Chest Rub: Add 1 ml oil and 5 drops chamomile oil to 10 ml carrier oil for asthmatic and bronchitic spasm.&lt;br /&gt;
 •	Hair Rinse: Dilute 5-10 drops of oil in water for lice, or use a few drops of neat oil on a fine comb for nits.&lt;br /&gt;
 •	Oil Apply undiluted to insect bites and stings: Dilute 10 drops oil in 25 ml carrier oil for sunstroke or to help prevent sunburn. &lt;br /&gt;
 •	Massage Oil: Dilute 1 ml &#039;lavender oil&#039; in 25 ml carrier oil, and massage into painful muscles.Dilute 10 drops in 25 ml carrier oil and massage into the temples and nape of the neck for tension headaches or at the first hint of a migraine.&lt;/div&gt;</summary>
		<author><name>Jy405</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It:Linalool&amp;diff=4951</id>
		<title>It:Linalool</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It:Linalool&amp;diff=4951"/>
		<updated>2006-11-06T15:56:58Z</updated>

		<summary type="html">&lt;p&gt;Jy405: /* Introduction */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;==Introduction==&lt;br /&gt;
Lavender is a shrubby plant in the mint family with about 25-30 species. It is native from the Mediterranean region south to tropical Afric and the east to India. The aromatic smell is found in all parts of the shrub, but the essential oil is only produced from the flowers and flower-stalks. The lavender flower oil is a complex mixture compounds containing linalool, linalyl acetate, 1, 8-cineole, β-ocimene and so on.&lt;br /&gt;
&lt;br /&gt;
[[Image:Lavender.jpg]]&lt;br /&gt;
&lt;br /&gt;
A picture of Lavender flower.&lt;br /&gt;
&lt;br /&gt;
==Linalool==&lt;br /&gt;
Linalool is a colourless fragrant liquid which can be found in many essential oil.&lt;br /&gt;
&lt;br /&gt;
[[Image:2D-structure_of_Linalool.gif]] &lt;br /&gt;
2D-strcture of Linalool&lt;br /&gt;
{| border=&amp;quot;1&amp;quot;&lt;br /&gt;
|+ The table&#039;s caption&lt;br /&gt;
!  !!&lt;br /&gt;
|-&lt;br /&gt;
! Einecs Number&lt;br /&gt;
| 201-134-4 ||&lt;br /&gt;
|-&lt;br /&gt;
! CAS Number&lt;br /&gt;
|78-70-6 ||&lt;br /&gt;
|-&lt;br /&gt;
! Chemical Name&lt;br /&gt;
|Linalool ||&lt;br /&gt;
|-&lt;br /&gt;
! Autoname&lt;br /&gt;
|3,7-Dimethyl-1,6-octadien-3-ol ||&lt;br /&gt;
|-&lt;br /&gt;
! Molecular Formula&lt;br /&gt;
|C10H18O||&lt;br /&gt;
|-&lt;br /&gt;
! Molecular Weight&lt;br /&gt;
|154.25 g/mol||&lt;br /&gt;
|-&lt;br /&gt;
! Physical State&lt;br /&gt;
|Clear to slightly yellow liquid||&lt;br /&gt;
|-&lt;br /&gt;
! Boiling Point&lt;br /&gt;
|198-200C||&lt;br /&gt;
|-&lt;br /&gt;
! Solubility in Water&lt;br /&gt;
|Insoluble||&lt;br /&gt;
|-&lt;br /&gt;
! Flash Point&lt;br /&gt;
|75C||&lt;br /&gt;
|-&lt;br /&gt;
! Toxicity&lt;br /&gt;
|Oral rat LD50: 2790 mg/kg||&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
==Synthesis of linalool==&lt;br /&gt;
Linalool is an anyclic alcohol. It has a sweet, pleasant fragrance and is one of the most frequently encountered floral scent compounds. Linalool has two enantiomeric forms (R) - linalool and (S) - linalool corresponds to the chiral properties of its hydroxylated third carbon. Traditionally, linalool was obtained from α- or β-pinene. The most modern synthesis start with 2-methyl-2-hepten-6-one and proceed via base-calalyzed ethynylation with acetylene to dehydrolinalool, yielding linalool through hydrogenation of the triple bond in the presence of a palladium-carbon catalyst.&lt;br /&gt;
&lt;br /&gt;
[[Image:Synthesis_of_Linalool_Molecule.gif]]&lt;br /&gt;
&lt;br /&gt;
The process of sysnthesising linalool molecule using 3,7-dimethyl-1,6-octadien-3-ol.&lt;br /&gt;
&lt;br /&gt;
==Uses of Lavender oil==&lt;br /&gt;
Generally its modern use is for aromatherapy. The research in lab showed that it helped in the reduction of advanced  mammory tumors in lab rats. Some other researches such as potential breast, ovarian, pancreatic, liver, and prostate cancer treatments are on-going.&lt;br /&gt;
Some advocates of alternative medicine claim that lavender oil can be used in a variety of variety.&lt;br /&gt;
 •	Cream: Add a few drops of oil to chamomile cream for eczema.&lt;br /&gt;
 •	Lotion: Add a few drops of oil to a little water for sunburn or scalds.&lt;br /&gt;
 •	Chest Rub: Add 1 ml oil and 5 drops chamomile oil to 10 ml carrier oil for asthmatic and bronchitic spasm.&lt;br /&gt;
 •	Hair Rinse: Dilute 5-10 drops of oil in water for lice, or use a few drops of neat oil on a fine comb for nits.&lt;br /&gt;
 •	Oil Apply undiluted to insect bites and stings: Dilute 10 drops oil in 25 ml carrier oil for sunstroke or to help prevent sunburn. &lt;br /&gt;
 •	Massage Oil: Dilute 1 ml &#039;lavender oil&#039; in 25 ml carrier oil, and massage into painful muscles.Dilute 10 drops in 25 ml carrier oil and massage into the temples and nape of the neck for tension headaches or at the first hint of a migraine.&lt;/div&gt;</summary>
		<author><name>Jy405</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=File:Lavender.jpg&amp;diff=4949</id>
		<title>File:Lavender.jpg</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=File:Lavender.jpg&amp;diff=4949"/>
		<updated>2006-11-06T15:55:41Z</updated>

		<summary type="html">&lt;p&gt;Jy405: A picture of Lavender&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;A picture of Lavender&lt;/div&gt;</summary>
		<author><name>Jy405</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It:Linalool&amp;diff=4946</id>
		<title>It:Linalool</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It:Linalool&amp;diff=4946"/>
		<updated>2006-11-06T15:53:16Z</updated>

		<summary type="html">&lt;p&gt;Jy405: /* Synthesis of linalool */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;==Introduction==&lt;br /&gt;
Lavender is a shrubby plant in the mint family with about 25-30 species. It is native from the Mediterranean region south to tropical Afric and the east to India. The aromatic smell is found in all parts of the shrub, but the essential oil is only produced from the flowers and flower-stalks. The lavender flower oil is a complex mixture compounds containing linalool, linalyl acetate, 1, 8-cineole, β-ocimene and so on. &lt;br /&gt;
==Linalool==&lt;br /&gt;
Linalool is a colourless fragrant liquid which can be found in many essential oil.&lt;br /&gt;
&lt;br /&gt;
[[Image:2D-structure_of_Linalool.gif]] &lt;br /&gt;
2D-strcture of Linalool&lt;br /&gt;
{| border=&amp;quot;1&amp;quot;&lt;br /&gt;
|+ The table&#039;s caption&lt;br /&gt;
!  !!&lt;br /&gt;
|-&lt;br /&gt;
! Einecs Number&lt;br /&gt;
| 201-134-4 ||&lt;br /&gt;
|-&lt;br /&gt;
! CAS Number&lt;br /&gt;
|78-70-6 ||&lt;br /&gt;
|-&lt;br /&gt;
! Chemical Name&lt;br /&gt;
|Linalool ||&lt;br /&gt;
|-&lt;br /&gt;
! Autoname&lt;br /&gt;
|3,7-Dimethyl-1,6-octadien-3-ol ||&lt;br /&gt;
|-&lt;br /&gt;
! Molecular Formula&lt;br /&gt;
|C10H18O||&lt;br /&gt;
|-&lt;br /&gt;
! Molecular Weight&lt;br /&gt;
|154.25 g/mol||&lt;br /&gt;
|-&lt;br /&gt;
! Physical State&lt;br /&gt;
|Clear to slightly yellow liquid||&lt;br /&gt;
|-&lt;br /&gt;
! Boiling Point&lt;br /&gt;
|198-200C||&lt;br /&gt;
|-&lt;br /&gt;
! Solubility in Water&lt;br /&gt;
|Insoluble||&lt;br /&gt;
|-&lt;br /&gt;
! Flash Point&lt;br /&gt;
|75C||&lt;br /&gt;
|-&lt;br /&gt;
! Toxicity&lt;br /&gt;
|Oral rat LD50: 2790 mg/kg||&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
==Synthesis of linalool==&lt;br /&gt;
Linalool is an anyclic alcohol. It has a sweet, pleasant fragrance and is one of the most frequently encountered floral scent compounds. Linalool has two enantiomeric forms (R) - linalool and (S) - linalool corresponds to the chiral properties of its hydroxylated third carbon. Traditionally, linalool was obtained from α- or β-pinene. The most modern synthesis start with 2-methyl-2-hepten-6-one and proceed via base-calalyzed ethynylation with acetylene to dehydrolinalool, yielding linalool through hydrogenation of the triple bond in the presence of a palladium-carbon catalyst.&lt;br /&gt;
&lt;br /&gt;
[[Image:Synthesis_of_Linalool_Molecule.gif]]&lt;br /&gt;
&lt;br /&gt;
The process of sysnthesising linalool molecule using 3,7-dimethyl-1,6-octadien-3-ol.&lt;br /&gt;
&lt;br /&gt;
==Uses of Lavender oil==&lt;br /&gt;
Generally its modern use is for aromatherapy. The research in lab showed that it helped in the reduction of advanced  mammory tumors in lab rats. Some other researches such as potential breast, ovarian, pancreatic, liver, and prostate cancer treatments are on-going.&lt;br /&gt;
Some advocates of alternative medicine claim that lavender oil can be used in a variety of variety.&lt;br /&gt;
 •	Cream: Add a few drops of oil to chamomile cream for eczema.&lt;br /&gt;
 •	Lotion: Add a few drops of oil to a little water for sunburn or scalds.&lt;br /&gt;
 •	Chest Rub: Add 1 ml oil and 5 drops chamomile oil to 10 ml carrier oil for asthmatic and bronchitic spasm.&lt;br /&gt;
 •	Hair Rinse: Dilute 5-10 drops of oil in water for lice, or use a few drops of neat oil on a fine comb for nits.&lt;br /&gt;
 •	Oil Apply undiluted to insect bites and stings: Dilute 10 drops oil in 25 ml carrier oil for sunstroke or to help prevent sunburn. &lt;br /&gt;
 •	Massage Oil: Dilute 1 ml &#039;lavender oil&#039; in 25 ml carrier oil, and massage into painful muscles.Dilute 10 drops in 25 ml carrier oil and massage into the temples and nape of the neck for tension headaches or at the first hint of a migraine.&lt;/div&gt;</summary>
		<author><name>Jy405</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=File:Synthesis_of_Linalool_Molecule.gif&amp;diff=4938</id>
		<title>File:Synthesis of Linalool Molecule.gif</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=File:Synthesis_of_Linalool_Molecule.gif&amp;diff=4938"/>
		<updated>2006-11-06T15:48:23Z</updated>

		<summary type="html">&lt;p&gt;Jy405: The process of sysnthesis of Linalool molecule.&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;The process of sysnthesis of Linalool molecule.&lt;/div&gt;</summary>
		<author><name>Jy405</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It:Linalool&amp;diff=4921</id>
		<title>It:Linalool</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It:Linalool&amp;diff=4921"/>
		<updated>2006-11-06T15:33:15Z</updated>

		<summary type="html">&lt;p&gt;Jy405: 2D-strcture of Linalool&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;==Introduction==&lt;br /&gt;
Lavender is a shrubby plant in the mint family with about 25-30 species. It is native from the Mediterranean region south to tropical Afric and the east to India. The aromatic smell is found in all parts of the shrub, but the essential oil is only produced from the flowers and flower-stalks. The lavender flower oil is a complex mixture compounds containing linalool, linalyl acetate, 1, 8-cineole, β-ocimene and so on. &lt;br /&gt;
==Linalool==&lt;br /&gt;
Linalool is a colourless fragrant liquid which can be found in many essential oil.&lt;br /&gt;
&lt;br /&gt;
[[Image:2D-structure_of_Linalool.gif]] &lt;br /&gt;
2D-strcture of Linalool&lt;br /&gt;
{| border=&amp;quot;1&amp;quot;&lt;br /&gt;
|+ The table&#039;s caption&lt;br /&gt;
!  !!&lt;br /&gt;
|-&lt;br /&gt;
! Einecs Number&lt;br /&gt;
| 201-134-4 ||&lt;br /&gt;
|-&lt;br /&gt;
! CAS Number&lt;br /&gt;
|78-70-6 ||&lt;br /&gt;
|-&lt;br /&gt;
! Chemical Name&lt;br /&gt;
|Linalool ||&lt;br /&gt;
|-&lt;br /&gt;
! Autoname&lt;br /&gt;
|3,7-Dimethyl-1,6-octadien-3-ol ||&lt;br /&gt;
|-&lt;br /&gt;
! Molecular Formula&lt;br /&gt;
|C10H18O||&lt;br /&gt;
|-&lt;br /&gt;
! Molecular Weight&lt;br /&gt;
|154.25 g/mol||&lt;br /&gt;
|-&lt;br /&gt;
! Physical State&lt;br /&gt;
|Clear to slightly yellow liquid||&lt;br /&gt;
|-&lt;br /&gt;
! Boiling Point&lt;br /&gt;
|198-200C||&lt;br /&gt;
|-&lt;br /&gt;
! Solubility in Water&lt;br /&gt;
|Insoluble||&lt;br /&gt;
|-&lt;br /&gt;
! Flash Point&lt;br /&gt;
|75C||&lt;br /&gt;
|-&lt;br /&gt;
! Toxicity&lt;br /&gt;
|Oral rat LD50: 2790 mg/kg||&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
==Synthesis of linalool==&lt;br /&gt;
Linalool is an anyclic alcohol. It has a sweet, pleasant fragrance and is one of the most frequently encountered floral scent compounds. Linalool has two enantiomeric forms (R) - linalool and (S) - linalool corresponds to the chiral properties of its hydroxylated third carbon. Traditionally, linalool was obtained from α- or β-pinene. The most modern synthesis start with 2-methyl-2-hepten-6-one and proceed via base-calalyzed ethynylation with acetylene to dehydrolinalool, yielding linalool through hydrogenation of the triple bond in the presence of a palladium-carbon catalyst.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==Uses of Lavender oil==&lt;br /&gt;
Generally its modern use is for aromatherapy. The research in lab showed that it helped in the reduction of advanced  mammory tumors in lab rats. Some other researches such as potential breast, ovarian, pancreatic, liver, and prostate cancer treatments are on-going.&lt;br /&gt;
Some advocates of alternative medicine claim that lavender oil can be used in a variety of variety.&lt;br /&gt;
 •	Cream: Add a few drops of oil to chamomile cream for eczema.&lt;br /&gt;
 •	Lotion: Add a few drops of oil to a little water for sunburn or scalds.&lt;br /&gt;
 •	Chest Rub: Add 1 ml oil and 5 drops chamomile oil to 10 ml carrier oil for asthmatic and bronchitic spasm.&lt;br /&gt;
 •	Hair Rinse: Dilute 5-10 drops of oil in water for lice, or use a few drops of neat oil on a fine comb for nits.&lt;br /&gt;
 •	Oil Apply undiluted to insect bites and stings: Dilute 10 drops oil in 25 ml carrier oil for sunstroke or to help prevent sunburn. &lt;br /&gt;
 •	Massage Oil: Dilute 1 ml &#039;lavender oil&#039; in 25 ml carrier oil, and massage into painful muscles.Dilute 10 drops in 25 ml carrier oil and massage into the temples and nape of the neck for tension headaches or at the first hint of a migraine.&lt;/div&gt;</summary>
		<author><name>Jy405</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=File:2D-structure_of_Linalool.gif&amp;diff=4916</id>
		<title>File:2D-structure of Linalool.gif</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=File:2D-structure_of_Linalool.gif&amp;diff=4916"/>
		<updated>2006-11-06T15:28:45Z</updated>

		<summary type="html">&lt;p&gt;Jy405: 2D-structure of Linalool&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;2D-structure of Linalool&lt;/div&gt;</summary>
		<author><name>Jy405</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It:Linalool&amp;diff=4894</id>
		<title>It:Linalool</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It:Linalool&amp;diff=4894"/>
		<updated>2006-11-06T11:19:17Z</updated>

		<summary type="html">&lt;p&gt;Jy405: /* Uses of Lavender oil */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;==Introduction==&lt;br /&gt;
Lavender is a shrubby plant in the mint family with about 25-30 species. It is native from the Mediterranean region south to tropical Afric and the east to India. The aromatic smell is found in all parts of the shrub, but the essential oil is only produced from the flowers and flower-stalks. The lavender flower oil is a complex mixture compounds containing linalool, linalyl acetate, 1, 8-cineole, β-ocimene and so on. &lt;br /&gt;
==Linalool==&lt;br /&gt;
Linalool is a colourless fragrant liquid which can be found in many essential oil.&lt;br /&gt;
{| border=&amp;quot;1&amp;quot;&lt;br /&gt;
|+ The table&#039;s caption&lt;br /&gt;
!  !!&lt;br /&gt;
|-&lt;br /&gt;
! Einecs Number&lt;br /&gt;
| 201-134-4 ||&lt;br /&gt;
|-&lt;br /&gt;
! CAS Number&lt;br /&gt;
|78-70-6 ||&lt;br /&gt;
|-&lt;br /&gt;
! Chemical Name&lt;br /&gt;
|Linalool ||&lt;br /&gt;
|-&lt;br /&gt;
! Autoname&lt;br /&gt;
|3,7-Dimethyl-1,6-octadien-3-ol ||&lt;br /&gt;
|-&lt;br /&gt;
! Molecular Formula&lt;br /&gt;
|C10H18O||&lt;br /&gt;
|-&lt;br /&gt;
! Molecular Weight&lt;br /&gt;
|154.25 g/mol||&lt;br /&gt;
|-&lt;br /&gt;
! Physical State&lt;br /&gt;
|Clear to slightly yellow liquid||&lt;br /&gt;
|-&lt;br /&gt;
! Boiling Point&lt;br /&gt;
|198-200C||&lt;br /&gt;
|-&lt;br /&gt;
! Solubility in Water&lt;br /&gt;
|Insoluble||&lt;br /&gt;
|-&lt;br /&gt;
! Flash Point&lt;br /&gt;
|75C||&lt;br /&gt;
|-&lt;br /&gt;
! Toxicity&lt;br /&gt;
|Oral rat LD50: 2790 mg/kg||&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
==Synthesis of linalool==&lt;br /&gt;
Linalool is an anyclic alcohol. It has a sweet, pleasant fragrance and is one of the most frequently encountered floral scent compounds. Linalool has two enantiomeric forms (R) - linalool and (S) - linalool corresponds to the chiral properties of its hydroxylated third carbon. Traditionally, linalool was obtained from α- or β-pinene. The most modern synthesis start with 2-methyl-2-hepten-6-one and proceed via base-calalyzed ethynylation with acetylene to dehydrolinalool, yielding linalool through hydrogenation of the triple bond in the presence of a palladium-carbon catalyst.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==Uses of Lavender oil==&lt;br /&gt;
Generally its modern use is for aromatherapy. The research in lab showed that it helped in the reduction of advanced  mammory tumors in lab rats. Some other researches such as potential breast, ovarian, pancreatic, liver, and prostate cancer treatments are on-going.&lt;br /&gt;
Some advocates of alternative medicine claim that lavender oil can be used in a variety of variety.&lt;br /&gt;
 •	Cream: Add a few drops of oil to chamomile cream for eczema.&lt;br /&gt;
 •	Lotion: Add a few drops of oil to a little water for sunburn or scalds.&lt;br /&gt;
 •	Chest Rub: Add 1 ml oil and 5 drops chamomile oil to 10 ml carrier oil for asthmatic and bronchitic spasm.&lt;br /&gt;
 •	Hair Rinse: Dilute 5-10 drops of oil in water for lice, or use a few drops of neat oil on a fine comb for nits.&lt;br /&gt;
 •	Oil Apply undiluted to insect bites and stings: Dilute 10 drops oil in 25 ml carrier oil for sunstroke or to help prevent sunburn. &lt;br /&gt;
 •	Massage Oil: Dilute 1 ml &#039;lavender oil&#039; in 25 ml carrier oil, and massage into painful muscles.Dilute 10 drops in 25 ml carrier oil and massage into the temples and nape of the neck for tension headaches or at the first hint of a migraine.&lt;/div&gt;</summary>
		<author><name>Jy405</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It:Linalool&amp;diff=4889</id>
		<title>It:Linalool</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It:Linalool&amp;diff=4889"/>
		<updated>2006-11-06T11:08:10Z</updated>

		<summary type="html">&lt;p&gt;Jy405: /* Uses of Lavender oil */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;==Introduction==&lt;br /&gt;
Lavender is a shrubby plant in the mint family with about 25-30 species. It is native from the Mediterranean region south to tropical Afric and the east to India. The aromatic smell is found in all parts of the shrub, but the essential oil is only produced from the flowers and flower-stalks. The lavender flower oil is a complex mixture compounds containing linalool, linalyl acetate, 1, 8-cineole, β-ocimene and so on. &lt;br /&gt;
==Linalool==&lt;br /&gt;
Linalool is a colourless fragrant liquid which can be found in many essential oil.&lt;br /&gt;
{| border=&amp;quot;1&amp;quot;&lt;br /&gt;
|+ The table&#039;s caption&lt;br /&gt;
!  !!&lt;br /&gt;
|-&lt;br /&gt;
! Einecs Number&lt;br /&gt;
| 201-134-4 ||&lt;br /&gt;
|-&lt;br /&gt;
! CAS Number&lt;br /&gt;
|78-70-6 ||&lt;br /&gt;
|-&lt;br /&gt;
! Chemical Name&lt;br /&gt;
|Linalool ||&lt;br /&gt;
|-&lt;br /&gt;
! Autoname&lt;br /&gt;
|3,7-Dimethyl-1,6-octadien-3-ol ||&lt;br /&gt;
|-&lt;br /&gt;
! Molecular Formula&lt;br /&gt;
|C10H18O||&lt;br /&gt;
|-&lt;br /&gt;
! Molecular Weight&lt;br /&gt;
|154.25 g/mol||&lt;br /&gt;
|-&lt;br /&gt;
! Physical State&lt;br /&gt;
|Clear to slightly yellow liquid||&lt;br /&gt;
|-&lt;br /&gt;
! Boiling Point&lt;br /&gt;
|198-200C||&lt;br /&gt;
|-&lt;br /&gt;
! Solubility in Water&lt;br /&gt;
|Insoluble||&lt;br /&gt;
|-&lt;br /&gt;
! Flash Point&lt;br /&gt;
|75C||&lt;br /&gt;
|-&lt;br /&gt;
! Toxicity&lt;br /&gt;
|Oral rat LD50: 2790 mg/kg||&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
==Synthesis of linalool==&lt;br /&gt;
Linalool is an anyclic alcohol. It has a sweet, pleasant fragrance and is one of the most frequently encountered floral scent compounds. Linalool has two enantiomeric forms (R) - linalool and (S) - linalool corresponds to the chiral properties of its hydroxylated third carbon. Traditionally, linalool was obtained from α- or β-pinene. The most modern synthesis start with 2-methyl-2-hepten-6-one and proceed via base-calalyzed ethynylation with acetylene to dehydrolinalool, yielding linalool through hydrogenation of the triple bond in the presence of a palladium-carbon catalyst.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==Uses of Lavender oil==&lt;br /&gt;
Generally its modern use is for aromatherapy. The research in lab showed that it helped in the reduction of advanced  mammory tumors in lab rats. Some other researches such as potential breast, ovarian, pancreatic, liver, and prostate cancer treatments are on-going.&lt;br /&gt;
Some advocates of alternative medicine claim that lavender oil can be used in a variety of variety.&lt;br /&gt;
(1)Cream Add a few drops of oil to chamomile cream for eczema. &lt;br /&gt;
(2)Lotion Add a few drops of oil to a little water for sunburn or scalds. &lt;br /&gt;
(3)Chest Rub Add 1 ml oil and 5 drops chamomile oil to 10 ml carrier oil for asthmatic and bronchitic spasm. &lt;br /&gt;
(4)Hair Rinse Dilute 5-10 drops of oil in water for lice, or use a few drops of neat oil on a fine comb for nits. &lt;br /&gt;
(5)Massage Oil Dilute 1 ml &#039;lavender oil&#039; in 25 ml carrier oil, and massage into painful muscles. Dilute 10 drops in 25 ml carrier oil and massage into the temples and nape of the neck for tension headaches or at the first hint of a migraine. &lt;br /&gt;
(6)Oil Apply undiluted to insect bites and stings. Dilute 10 drops oil in 25 ml carrier oil for sunstroke or to help prevent sunburn. (Note: this is not an effective sunblock.)&lt;/div&gt;</summary>
		<author><name>Jy405</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It:Linalool&amp;diff=4888</id>
		<title>It:Linalool</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It:Linalool&amp;diff=4888"/>
		<updated>2006-11-06T10:50:09Z</updated>

		<summary type="html">&lt;p&gt;Jy405: Uses of Lavender oil&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;==Introduction==&lt;br /&gt;
Lavender is a shrubby plant in the mint family with about 25-30 species. It is native from the Mediterranean region south to tropical Afric and the east to India. The aromatic smell is found in all parts of the shrub, but the essential oil is only produced from the flowers and flower-stalks. The lavender flower oil is a complex mixture compounds containing linalool, linalyl acetate, 1, 8-cineole, β-ocimene and so on. &lt;br /&gt;
==Linalool==&lt;br /&gt;
Linalool is a colourless fragrant liquid which can be found in many essential oil.&lt;br /&gt;
{| border=&amp;quot;1&amp;quot;&lt;br /&gt;
|+ The table&#039;s caption&lt;br /&gt;
!  !!&lt;br /&gt;
|-&lt;br /&gt;
! Einecs Number&lt;br /&gt;
| 201-134-4 ||&lt;br /&gt;
|-&lt;br /&gt;
! CAS Number&lt;br /&gt;
|78-70-6 ||&lt;br /&gt;
|-&lt;br /&gt;
! Chemical Name&lt;br /&gt;
|Linalool ||&lt;br /&gt;
|-&lt;br /&gt;
! Autoname&lt;br /&gt;
|3,7-Dimethyl-1,6-octadien-3-ol ||&lt;br /&gt;
|-&lt;br /&gt;
! Molecular Formula&lt;br /&gt;
|C10H18O||&lt;br /&gt;
|-&lt;br /&gt;
! Molecular Weight&lt;br /&gt;
|154.25 g/mol||&lt;br /&gt;
|-&lt;br /&gt;
! Physical State&lt;br /&gt;
|Clear to slightly yellow liquid||&lt;br /&gt;
|-&lt;br /&gt;
! Boiling Point&lt;br /&gt;
|198-200C||&lt;br /&gt;
|-&lt;br /&gt;
! Solubility in Water&lt;br /&gt;
|Insoluble||&lt;br /&gt;
|-&lt;br /&gt;
! Flash Point&lt;br /&gt;
|75C||&lt;br /&gt;
|-&lt;br /&gt;
! Toxicity&lt;br /&gt;
|Oral rat LD50: 2790 mg/kg||&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
==Synthesis of linalool==&lt;br /&gt;
Linalool is an anyclic alcohol. It has a sweet, pleasant fragrance and is one of the most frequently encountered floral scent compounds. Linalool has two enantiomeric forms (R) - linalool and (S) - linalool corresponds to the chiral properties of its hydroxylated third carbon. Traditionally, linalool was obtained from α- or β-pinene. The most modern synthesis start with 2-methyl-2-hepten-6-one and proceed via base-calalyzed ethynylation with acetylene to dehydrolinalool, yielding linalool through hydrogenation of the triple bond in the presence of a palladium-carbon catalyst.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==Uses of Lavender oil==&lt;br /&gt;
Generally its modern use is for aromatherapy. The research in lab showed that it helped in the reduction of advanced  mammory tumors in lab rats. Some other researches such as potential breast, ovarian, pancreatic, liver, and prostate cancer treatments are on-going.&lt;br /&gt;
Some advocates of alternative medicine claim that lavender oil can be used in a variety of variety.&lt;br /&gt;
•Cream Add a few drops of oil to chamomile cream for eczema. &lt;br /&gt;
•Lotion Add a few drops of oil to a little water for sunburn or scalds. &lt;br /&gt;
•Chest Rub Add 1 ml oil and 5 drops chamomile oil to 10 ml carrier oil for asthmatic and bronchitic spasm. &lt;br /&gt;
•Hair Rinse Dilute 5-10 drops of oil in water for lice, or use a few drops of neat oil on a fine comb for nits. &lt;br /&gt;
•Massage Oil Dilute 1 ml &#039;lavender oil&#039; in 25 ml carrier oil, and massage into painful muscles. Dilute 10 drops in 25 ml carrier oil and massage into the temples and nape of the neck for tension headaches or at the first hint of a migraine. &lt;br /&gt;
•Oil Apply undiluted to insect bites and stings. Dilute 10 drops oil in 25 ml carrier oil for sunstroke or to help prevent sunburn. (Note: this is not an effective sunblock.)&lt;/div&gt;</summary>
		<author><name>Jy405</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It:Linalool&amp;diff=4878</id>
		<title>It:Linalool</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It:Linalool&amp;diff=4878"/>
		<updated>2006-11-05T15:58:58Z</updated>

		<summary type="html">&lt;p&gt;Jy405: Synthesis of Linalool&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;==Introduction==&lt;br /&gt;
Lavender is a shrubby plant in the mint family with about 25-30 species. It is native from the Mediterranean region south to tropical Afric and the east to India. The aromatic smell is found in all parts of the shrub, but the essential oil is only produced from the flowers and flower-stalks. The lavender flower oil is a complex mixture compounds containing linalool, linalyl acetate, 1, 8-cineole, β-ocimene and so on. &lt;br /&gt;
==Linalool==&lt;br /&gt;
Linalool is a colourless fragrant liquid which can be found in many essential oil.&lt;br /&gt;
{| border=&amp;quot;1&amp;quot;&lt;br /&gt;
|+ The table&#039;s caption&lt;br /&gt;
!  !!&lt;br /&gt;
|-&lt;br /&gt;
! Einecs Number&lt;br /&gt;
| 201-134-4 ||&lt;br /&gt;
|-&lt;br /&gt;
! CAS Number&lt;br /&gt;
|78-70-6 ||&lt;br /&gt;
|-&lt;br /&gt;
! Chemical Name&lt;br /&gt;
|Linalool ||&lt;br /&gt;
|-&lt;br /&gt;
! Autoname&lt;br /&gt;
|3,7-Dimethyl-1,6-octadien-3-ol ||&lt;br /&gt;
|-&lt;br /&gt;
! Molecular Formula&lt;br /&gt;
|C10H18O||&lt;br /&gt;
|-&lt;br /&gt;
! Molecular Weight&lt;br /&gt;
|154.25 g/mol||&lt;br /&gt;
|-&lt;br /&gt;
! Physical State&lt;br /&gt;
|Clear to slightly yellow liquid||&lt;br /&gt;
|-&lt;br /&gt;
! Boiling Point&lt;br /&gt;
|198-200C||&lt;br /&gt;
|-&lt;br /&gt;
! Solubility in Water&lt;br /&gt;
|Insoluble||&lt;br /&gt;
|-&lt;br /&gt;
! Flash Point&lt;br /&gt;
|75C||&lt;br /&gt;
|-&lt;br /&gt;
! Toxicity&lt;br /&gt;
|Oral rat LD50: 2790 mg/kg||&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
==Synthesis of linalool==&lt;br /&gt;
Linalool is an anyclic alcohol. It has a sweet, pleasant fragrance and is one of the most frequently encountered floral scent compounds. Linalool has two enantiomeric forms (R) - linalool and (S) - linalool corresponds to the chiral properties of its hydroxylated third carbon. Traditionally, linalool was obtained from α- or β-pinene. The most modern synthesis start with 2-methyl-2-hepten-6-one and proceed via base-calalyzed ethynylation with acetylene to dehydrolinalool, yielding linalool through hydrogenation of the triple bond in the presence of a palladium-carbon catalyst.&lt;/div&gt;</summary>
		<author><name>Jy405</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It:projects&amp;diff=4877</id>
		<title>It:projects</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It:projects&amp;diff=4877"/>
		<updated>2006-11-05T15:44:56Z</updated>

		<summary type="html">&lt;p&gt;Jy405: /* Supplemental  Project Page */&lt;/p&gt;
&lt;hr /&gt;
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|-&lt;br /&gt;
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| bgcolor=&amp;quot;#CCFF00&amp;quot; |11&lt;br /&gt;
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| bgcolor=&amp;quot;#CCFF00&amp;quot; |13&lt;br /&gt;
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| bgcolor=&amp;quot;#CCFF00&amp;quot; |16&lt;br /&gt;
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| bgcolor=&amp;quot;#CCFF00&amp;quot; |17&lt;br /&gt;
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| bgcolor=&amp;quot;#CCFF00&amp;quot; |18&lt;br /&gt;
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| bgcolor=&amp;quot;#CCFF00&amp;quot; |19&lt;br /&gt;
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| bgcolor=&amp;quot;#CCFF00&amp;quot; |20&lt;br /&gt;
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[[Template:Chem-Data]]&lt;/div&gt;</summary>
		<author><name>Jy405</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It:Linalool&amp;diff=4876</id>
		<title>It:Linalool</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It:Linalool&amp;diff=4876"/>
		<updated>2006-11-05T15:42:50Z</updated>

		<summary type="html">&lt;p&gt;Jy405: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;==Introduction==&lt;br /&gt;
Lavender is a shrubby plant in the mint family with about 25-30 species. It is native from the Mediterranean region south to tropical Afric and the east to India. The aromatic smell is found in all parts of the shrub, but the essential oil is only produced from the flowers and flower-stalks. The lavender flower oil is a complex mixture compounds containing linalool, linalyl acetate, 1, 8-cineole, β-ocimene and so on. &lt;br /&gt;
==Linalool==&lt;br /&gt;
Linalool is a colourless fragrant liquid which can be found in many essential oil.&lt;br /&gt;
{| border=&amp;quot;1&amp;quot;&lt;br /&gt;
|+ The table&#039;s caption&lt;br /&gt;
!  !!&lt;br /&gt;
|-&lt;br /&gt;
! Einecs Number&lt;br /&gt;
| 201-134-4 ||&lt;br /&gt;
|-&lt;br /&gt;
! CAS Number&lt;br /&gt;
|78-70-6 ||&lt;br /&gt;
|-&lt;br /&gt;
! Chemical Name&lt;br /&gt;
|Linalool ||&lt;br /&gt;
|-&lt;br /&gt;
! Autoname&lt;br /&gt;
|3,7-Dimethyl-1,6-octadien-3-ol ||&lt;br /&gt;
|-&lt;br /&gt;
! Molecular Formula&lt;br /&gt;
|C10H18O||&lt;br /&gt;
|-&lt;br /&gt;
! Molecular Weight&lt;br /&gt;
|154.25 g/mol||&lt;br /&gt;
|-&lt;br /&gt;
! Physical State&lt;br /&gt;
|Clear to slightly yellow liquid||&lt;br /&gt;
|-&lt;br /&gt;
! Boiling Point&lt;br /&gt;
|198-200C||&lt;br /&gt;
|-&lt;br /&gt;
! Solubility in Water&lt;br /&gt;
|Insoluble||&lt;br /&gt;
|-&lt;br /&gt;
! Flash Point&lt;br /&gt;
|75C||&lt;br /&gt;
|-&lt;br /&gt;
! Toxicity&lt;br /&gt;
|Oral rat LD50: 2790 mg/kg||&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
|}&lt;/div&gt;</summary>
		<author><name>Jy405</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It:Linalool&amp;diff=4875</id>
		<title>It:Linalool</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It:Linalool&amp;diff=4875"/>
		<updated>2006-11-05T14:54:47Z</updated>

		<summary type="html">&lt;p&gt;Jy405: Physical properties&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;Lavender is a shrubby plant in the mint family with about 25-30 species. It is native from the Mediterranean region south to tropical Afric and the east to India. The aromatic smell is found in all parts of the shrub, but the essential oil is only produced from the flowers and flower-stalks. The lavender flower oil is a complex mixture compounds containing linalool, linalyl acetate, 1, 8-cineole, β-ocimene and so on. &lt;br /&gt;
&lt;br /&gt;
Linalool is a colourless fragrant liquid which can be found in many essential oil.&lt;br /&gt;
{| border=&amp;quot;1&amp;quot;&lt;br /&gt;
|+ The table&#039;s caption&lt;br /&gt;
!  !!&lt;br /&gt;
|-&lt;br /&gt;
! Einecs Number&lt;br /&gt;
| 201-134-4 ||&lt;br /&gt;
|-&lt;br /&gt;
! CAS Number&lt;br /&gt;
|78-70-6 ||&lt;br /&gt;
|-&lt;br /&gt;
! Chemical Name&lt;br /&gt;
|Linalool ||&lt;br /&gt;
|-&lt;br /&gt;
! Autoname&lt;br /&gt;
|3,7-Dimethyl-1,6-octadien-3-ol ||&lt;br /&gt;
|-&lt;br /&gt;
! Molecular Formula&lt;br /&gt;
|C10H18O||&lt;br /&gt;
|-&lt;br /&gt;
! Molecular Weight&lt;br /&gt;
|154.25 g/mol||&lt;br /&gt;
|-&lt;br /&gt;
! Physical State&lt;br /&gt;
|Clear to slightly yellow liquid||&lt;br /&gt;
|-&lt;br /&gt;
! Boiling Point&lt;br /&gt;
|198-200C||&lt;br /&gt;
|-&lt;br /&gt;
! Solubility in Water&lt;br /&gt;
|Insoluble||&lt;br /&gt;
|-&lt;br /&gt;
! Flash Point&lt;br /&gt;
|75C||&lt;br /&gt;
|-&lt;br /&gt;
! Stability&lt;br /&gt;
|Stable under ordinary conditions||&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
|}&lt;/div&gt;</summary>
		<author><name>Jy405</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It:Linalool&amp;diff=4842</id>
		<title>It:Linalool</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It:Linalool&amp;diff=4842"/>
		<updated>2006-11-04T16:53:21Z</updated>

		<summary type="html">&lt;p&gt;Jy405: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;Lavender is a shrubby plant in the mint family with about 25-30 species. It is native from the Mediterranean region south to tropical Afric and the east to India. The aromatic smell is found in all parts of the shrub, but the essential oil is only produced from the flowers and flower-stalks. The lavender flower oil is a complex mixture compounds containing linalool, linalyl acetate, 1, 8-cineole, β-ocimene and so on. &lt;br /&gt;
&lt;br /&gt;
Linalool is a colourless fragrant liquid which can be found in many essential oil.&lt;/div&gt;</summary>
		<author><name>Jy405</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It:projects&amp;diff=4841</id>
		<title>It:projects</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It:projects&amp;diff=4841"/>
		<updated>2006-11-04T16:51:33Z</updated>

		<summary type="html">&lt;p&gt;Jy405: /* Export Pages */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;__FORCETOC__&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;&#039;&#039;You MUST use the  Edit buttons on the right to edit this content.  Do NOT use the Edit button on the top of this page.&#039;&#039;&#039;&#039;&#039;&lt;br /&gt;
== Sandbox (Play-Pen) ==	 &lt;br /&gt;
		 &lt;br /&gt;
This is an area where you can play without worrying what you do. Enter it by pressing the [Edit] button &#039;&#039;&#039;on the right&#039;&#039;&#039; and &#039;&#039;&#039;not&#039;&#039;&#039; at the top. Go here for a [http://en.wikipedia.org/wiki/Wikipedia:Cheatsheet &#039;&#039;cheat sheet&#039;&#039;] summary of how to create a Wiki page.	 It&#039;s a free-for-all in here! Learn how to use a Wiki by coming here! PS This is how to do Greek: &amp;amp;Alpha;, &amp;amp;alpha;, &amp;amp;beta; &amp;amp;Delta;, &amp;amp;delta;	 		 &lt;br /&gt;
Try copying/pasting some of the [http://www.ch.ic.ac.uk/local/it/lab1.html examples in the course work] into this page. See the effect by selecting &#039;&#039;&#039;Show Preview&#039;&#039;&#039;. No not use &#039;&#039;&#039;Save Page&#039;&#039;&#039; so as to leave this area uncluttered for others.&lt;br /&gt;
----&lt;br /&gt;
&lt;br /&gt;
== Main Project Page ==&lt;br /&gt;
&#039;&#039;&#039;Please do not edit this page itself&#039;&#039;&#039;.  Click on one of the titles to start editing.&lt;br /&gt;
{| summary=&amp;quot;CIT Project  Titles&amp;quot; border=&amp;quot;1&amp;quot;&lt;br /&gt;
! bgcolor=&amp;quot;cyan&amp;quot; |Project&amp;lt;br /&amp;gt; Number&lt;br /&gt;
! bgcolor=&amp;quot;cyan&amp;quot; |General Keywords&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |01&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; | [[it:Lignocaine|Lignocaine (used in dentistry as a &amp;quot;local&amp;quot;)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |02&lt;br /&gt;
| bgcolor=&amp;quot;#66FF99&amp;quot; | [[it:Piperine|Piperine (active ingredient of both black and white pepper)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |03&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; | [[it:Rapamycin|Rapamycin (prevents transplant rejection)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |04&lt;br /&gt;
| bgcolor=&amp;quot;#66FF99&amp;quot; | [[it:Gossypol|Gossypol (male birth control)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |05&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; | [[it:Gentamycin|Gentamicin A (aminoglycoside antibiotic)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |06&lt;br /&gt;
| bgcolor=&amp;quot;#66FF99&amp;quot; | [[it:Herceptin|Herceptin (topical anticancer drug)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |07&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; | [[it:Gingerone|Zingerone (the characteristic smell of ginger)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |08&lt;br /&gt;
| bgcolor=&amp;quot;#66FF99&amp;quot; | [[it:Sucralose|Sucralose (non-metabolizable sweetening agent)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |09&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; | [[it:Bufotoxin|Bufotoxin (active component of the toad &#039;&#039;Bufo vulgaris&#039;&#039;)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |10&lt;br /&gt;
| bgcolor=&amp;quot;#66FF99&amp;quot; | [[it:Roaccutane|Roaccutane (treatment for severe acne)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |11&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; | [[it:Sibutramine|Sibutramine (appetite suppresor)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |12&lt;br /&gt;
| bgcolor=&amp;quot;#66FF99&amp;quot; | [[it:Anandamide|Anandamide (the &amp;quot;feel-good&amp;quot; factor in chocolate)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |13&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; | [[it:h3nbh3|Ammonia-borane: H&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;N-BH&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt; (Hydrogen storage molecule?)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |14&lt;br /&gt;
| bgcolor=&amp;quot;#66FF99&amp;quot; | [[it:Methoxsalen|Methoxsalen (Treatment of psoriasis)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |15&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; | [[it:Hycocine|Hyoscine (From Mandrake and Witches Henbane, pre-med before surgery)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |16&lt;br /&gt;
| bgcolor=&amp;quot;#66FF99&amp;quot; | [[it:Capreomycin|Capreomycin (Drug-resistant TB)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |17&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; | [[it:wilkinson|Wilkinson&#039;s catalyst]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |18&lt;br /&gt;
| bgcolor=&amp;quot;#66FF99&amp;quot; | [[it:Jacobsen|Jacobsen&#039;s epoxidation catalyst]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |19&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; | [[it:Methylaluminoxane|Methylaluminoxane: MAO - hugely important ethylene polymerisation cocatalyst]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |20&lt;br /&gt;
| bgcolor=&amp;quot;#66FF99&amp;quot; | [[it:Schwartz|Schwartz reagent for the hydrozirconation of alkenes and alkynes]]&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
== Supplemental  Project Page ==&lt;br /&gt;
&lt;br /&gt;
This area is for people who wish to create their own projects if none of the above appeal to them. Click on the  &#039;&#039;&#039;Edit&#039;&#039;&#039;  button to the right to open up an editable page,&lt;br /&gt;
then add an entry below as follows&lt;br /&gt;
&lt;br /&gt;
*&amp;lt;nowiki&amp;gt; [[it:name_of_project|Descriptive name of intended project]]&amp;lt;/nowiki&amp;gt;&lt;br /&gt;
*This will produce the effect:  [[it:name_of_project|Descriptive name of intended project]]&lt;br /&gt;
----&lt;br /&gt;
*[[it:sitagliptin_page|Sitagliptin]]&lt;br /&gt;
*[[it:Retinal|Retinal, molecule of sight]]&lt;br /&gt;
*[[it:Tamoxifen|Tamoxifen, breast cancer treatment]]&lt;br /&gt;
*[[it:Morphine|Morphine, painkiller]]&lt;br /&gt;
*[[it:Pelargonidin|Pelargonidin, colouring in nature]]&lt;br /&gt;
*[[it:Propanil|Propanil, weedkiller]]&lt;br /&gt;
*[[it:Ranitidine|Ranitidine, antiulcerative]]&lt;br /&gt;
*[[it:chlorphentermine|chlorphentermine, anorectic]]&lt;br /&gt;
*[[it:Serotonin|Serotonin, The &#039;HAPPY&#039; Drug]]&lt;br /&gt;
*[[it:Amphidinolide T1|Amphidinolide T1]]&lt;br /&gt;
*[[it:Rosiglitazone|Rosiglitazone, drug that is currently used to treat diabetes.]]&lt;br /&gt;
*[[it:Furosemide|Furosemide]]&lt;br /&gt;
*[[it:Tryptophan|Tryptophan]]&lt;br /&gt;
*[[it:methylpentynol|methylpentynol, tranquilliser.]]&lt;br /&gt;
*[[it:Ferrocene|Ferrocene]]&lt;br /&gt;
*[[it:Scopolamine|Scopolamine, the (Former) Truth Drug]]&lt;br /&gt;
*[[it:Camptothecin|Camptothecin,Anti-cancer agent ]]&lt;br /&gt;
*[[it:Salmeterol|Salmeterol, an agonist used to treat asthma]]&lt;br /&gt;
*[[it:Psilocin|Psilocin]]&lt;br /&gt;
*[[it:Epibatidine|Epibatidine]]&lt;br /&gt;
*[[it:Beta Carotene|Beta Carotene]]&lt;br /&gt;
*[[it:Thyroxine|Thyroxine, the Thyroid Hormone]]&lt;br /&gt;
*[[it:Tetrahydrocannabinol|Tetrahydrocannabinol]]&lt;br /&gt;
*[[it:Linalool|A component of essential oil]]&lt;br /&gt;
&lt;br /&gt;
== [[Special:Export|Export Pages]] ==&lt;br /&gt;
&lt;br /&gt;
== Overlaps ==&lt;br /&gt;
&lt;br /&gt;
If two people start editing a page at the same time, and  &#039;&#039;&#039;save&#039;&#039;&#039; the change simultaneously, its possible only one of the changes&lt;br /&gt;
will be made permanent.  If anyone spots this happening, please let  me know. &lt;br /&gt;
&lt;br /&gt;
One precaution you could take is to keep a copy of the contents of the page you are editing in eg Wordpad (or Word),&lt;br /&gt;
make the changes there, and then copy the entire lot to the  Wiki page to preview and then save. Tht way, if your contribution&lt;br /&gt;
is overlapped by someone else, you will still have a copy, and you can then resubmit it.&lt;br /&gt;
----&lt;br /&gt;
--[[User:Rzepa|Rzepa]] 12:25, 19 October 2006 (BST)&lt;br /&gt;
&lt;br /&gt;
== Wiki Utillities ==&lt;br /&gt;
Utilities have been written to help the conversion of material from  HTML.&lt;br /&gt;
&lt;br /&gt;
# [http://diberri.dyndns.org/wikipedia/html2wiki/ A HTML2Wiki Converter]&lt;br /&gt;
&lt;br /&gt;
No wiki2html converter suitable for use has yet been identified.&lt;br /&gt;
=== Wiki Templates ===&lt;br /&gt;
&lt;br /&gt;
[[Template:DOI]] and [[Template:Doi-inline]] are providea as (protected) templates for your use.  Many other templates exist, often to be found on e.g. Wikipedia pages.  You may decide one of these is of particular use, or of interest.  If so, you can install it on the wiki here for you and others to use.  Add below a line that looks like  {{template-name|parameter}}, save, and click on the red text to create the new template. If you prefer the task of adding useful templates to that of adding information about molecules, then you will be given full credit for performing this valuable service for others!&lt;br /&gt;
--[[User:Rzepa|Rzepa]] 14:41, 20 October 2006 (BST)&lt;br /&gt;
&lt;br /&gt;
----&lt;br /&gt;
[[Template:Chem-Data]]&lt;/div&gt;</summary>
		<author><name>Jy405</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It:projects&amp;diff=4840</id>
		<title>It:projects</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It:projects&amp;diff=4840"/>
		<updated>2006-11-04T16:49:53Z</updated>

		<summary type="html">&lt;p&gt;Jy405: /* Export Pages */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;__FORCETOC__&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;&#039;&#039;You MUST use the  Edit buttons on the right to edit this content.  Do NOT use the Edit button on the top of this page.&#039;&#039;&#039;&#039;&#039;&lt;br /&gt;
== Sandbox (Play-Pen) ==	 &lt;br /&gt;
		 &lt;br /&gt;
This is an area where you can play without worrying what you do. Enter it by pressing the [Edit] button &#039;&#039;&#039;on the right&#039;&#039;&#039; and &#039;&#039;&#039;not&#039;&#039;&#039; at the top. Go here for a [http://en.wikipedia.org/wiki/Wikipedia:Cheatsheet &#039;&#039;cheat sheet&#039;&#039;] summary of how to create a Wiki page.	 It&#039;s a free-for-all in here! Learn how to use a Wiki by coming here! PS This is how to do Greek: &amp;amp;Alpha;, &amp;amp;alpha;, &amp;amp;beta; &amp;amp;Delta;, &amp;amp;delta;	 		 &lt;br /&gt;
Try copying/pasting some of the [http://www.ch.ic.ac.uk/local/it/lab1.html examples in the course work] into this page. See the effect by selecting &#039;&#039;&#039;Show Preview&#039;&#039;&#039;. No not use &#039;&#039;&#039;Save Page&#039;&#039;&#039; so as to leave this area uncluttered for others.&lt;br /&gt;
----&lt;br /&gt;
&lt;br /&gt;
== Main Project Page ==&lt;br /&gt;
&#039;&#039;&#039;Please do not edit this page itself&#039;&#039;&#039;.  Click on one of the titles to start editing.&lt;br /&gt;
{| summary=&amp;quot;CIT Project  Titles&amp;quot; border=&amp;quot;1&amp;quot;&lt;br /&gt;
! bgcolor=&amp;quot;cyan&amp;quot; |Project&amp;lt;br /&amp;gt; Number&lt;br /&gt;
! bgcolor=&amp;quot;cyan&amp;quot; |General Keywords&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |01&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; | [[it:Lignocaine|Lignocaine (used in dentistry as a &amp;quot;local&amp;quot;)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |02&lt;br /&gt;
| bgcolor=&amp;quot;#66FF99&amp;quot; | [[it:Piperine|Piperine (active ingredient of both black and white pepper)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |03&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; | [[it:Rapamycin|Rapamycin (prevents transplant rejection)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |04&lt;br /&gt;
| bgcolor=&amp;quot;#66FF99&amp;quot; | [[it:Gossypol|Gossypol (male birth control)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |05&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; | [[it:Gentamycin|Gentamicin A (aminoglycoside antibiotic)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |06&lt;br /&gt;
| bgcolor=&amp;quot;#66FF99&amp;quot; | [[it:Herceptin|Herceptin (topical anticancer drug)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |07&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; | [[it:Gingerone|Zingerone (the characteristic smell of ginger)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |08&lt;br /&gt;
| bgcolor=&amp;quot;#66FF99&amp;quot; | [[it:Sucralose|Sucralose (non-metabolizable sweetening agent)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |09&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; | [[it:Bufotoxin|Bufotoxin (active component of the toad &#039;&#039;Bufo vulgaris&#039;&#039;)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |10&lt;br /&gt;
| bgcolor=&amp;quot;#66FF99&amp;quot; | [[it:Roaccutane|Roaccutane (treatment for severe acne)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |11&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; | [[it:Sibutramine|Sibutramine (appetite suppresor)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |12&lt;br /&gt;
| bgcolor=&amp;quot;#66FF99&amp;quot; | [[it:Anandamide|Anandamide (the &amp;quot;feel-good&amp;quot; factor in chocolate)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |13&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; | [[it:h3nbh3|Ammonia-borane: H&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;N-BH&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt; (Hydrogen storage molecule?)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |14&lt;br /&gt;
| bgcolor=&amp;quot;#66FF99&amp;quot; | [[it:Methoxsalen|Methoxsalen (Treatment of psoriasis)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |15&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; | [[it:Hycocine|Hyoscine (From Mandrake and Witches Henbane, pre-med before surgery)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |16&lt;br /&gt;
| bgcolor=&amp;quot;#66FF99&amp;quot; | [[it:Capreomycin|Capreomycin (Drug-resistant TB)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |17&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; | [[it:wilkinson|Wilkinson&#039;s catalyst]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |18&lt;br /&gt;
| bgcolor=&amp;quot;#66FF99&amp;quot; | [[it:Jacobsen|Jacobsen&#039;s epoxidation catalyst]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |19&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; | [[it:Methylaluminoxane|Methylaluminoxane: MAO - hugely important ethylene polymerisation cocatalyst]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |20&lt;br /&gt;
| bgcolor=&amp;quot;#66FF99&amp;quot; | [[it:Schwartz|Schwartz reagent for the hydrozirconation of alkenes and alkynes]]&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
== Supplemental  Project Page ==&lt;br /&gt;
&lt;br /&gt;
This area is for people who wish to create their own projects if none of the above appeal to them. Click on the  &#039;&#039;&#039;Edit&#039;&#039;&#039;  button to the right to open up an editable page,&lt;br /&gt;
then add an entry below as follows&lt;br /&gt;
&lt;br /&gt;
*&amp;lt;nowiki&amp;gt; [[it:name_of_project|Descriptive name of intended project]]&amp;lt;/nowiki&amp;gt;&lt;br /&gt;
*This will produce the effect:  [[it:name_of_project|Descriptive name of intended project]]&lt;br /&gt;
----&lt;br /&gt;
*[[it:sitagliptin_page|Sitagliptin]]&lt;br /&gt;
*[[it:Retinal|Retinal, molecule of sight]]&lt;br /&gt;
*[[it:Tamoxifen|Tamoxifen, breast cancer treatment]]&lt;br /&gt;
*[[it:Morphine|Morphine, painkiller]]&lt;br /&gt;
*[[it:Pelargonidin|Pelargonidin, colouring in nature]]&lt;br /&gt;
*[[it:Propanil|Propanil, weedkiller]]&lt;br /&gt;
*[[it:Ranitidine|Ranitidine, antiulcerative]]&lt;br /&gt;
*[[it:chlorphentermine|chlorphentermine, anorectic]]&lt;br /&gt;
*[[it:Serotonin|Serotonin, The &#039;HAPPY&#039; Drug]]&lt;br /&gt;
*[[it:Amphidinolide T1|Amphidinolide T1]]&lt;br /&gt;
*[[it:Rosiglitazone|Rosiglitazone, drug that is currently used to treat diabetes.]]&lt;br /&gt;
*[[it:Furosemide|Furosemide]]&lt;br /&gt;
*[[it:Tryptophan|Tryptophan]]&lt;br /&gt;
*[[it:methylpentynol|methylpentynol, tranquilliser.]]&lt;br /&gt;
*[[it:Ferrocene|Ferrocene]]&lt;br /&gt;
*[[it:Scopolamine|Scopolamine, the (Former) Truth Drug]]&lt;br /&gt;
*[[it:Camptothecin|Camptothecin,Anti-cancer agent ]]&lt;br /&gt;
*[[it:Salmeterol|Salmeterol, an agonist used to treat asthma]]&lt;br /&gt;
*[[it:Psilocin|Psilocin]]&lt;br /&gt;
*[[it:Epibatidine|Epibatidine]]&lt;br /&gt;
*[[it:Beta Carotene|Beta Carotene]]&lt;br /&gt;
*[[it:Thyroxine|Thyroxine, the Thyroid Hormone]]&lt;br /&gt;
*[[it:Tetrahydrocannabinol|Tetrahydrocannabinol]]&lt;br /&gt;
*[[it:Linalool|A component of essential oil]]&lt;br /&gt;
&lt;br /&gt;
== [[Special:Export|Export Pages]] ==&lt;br /&gt;
Lavender is a shrubby plant in the mint family with about 25-30 species. It is native from the Mediterranean region south to tropical Afric and the east to India. The aromatic smell is found in all parts of the shrub, but the essential oil is only produced from the flowers and flower-stalks. The lavender flower oil is a complex mixture compounds containing linalool, linalyl acetate, 1, 8-cineole, β-ocimene and so on.&lt;br /&gt;
&lt;br /&gt;
Linalool is a colourless fragrant liquid which can be found in many essential oil.&lt;br /&gt;
&lt;br /&gt;
== Overlaps ==&lt;br /&gt;
&lt;br /&gt;
If two people start editing a page at the same time, and  &#039;&#039;&#039;save&#039;&#039;&#039; the change simultaneously, its possible only one of the changes&lt;br /&gt;
will be made permanent.  If anyone spots this happening, please let  me know. &lt;br /&gt;
&lt;br /&gt;
One precaution you could take is to keep a copy of the contents of the page you are editing in eg Wordpad (or Word),&lt;br /&gt;
make the changes there, and then copy the entire lot to the  Wiki page to preview and then save. Tht way, if your contribution&lt;br /&gt;
is overlapped by someone else, you will still have a copy, and you can then resubmit it.&lt;br /&gt;
----&lt;br /&gt;
--[[User:Rzepa|Rzepa]] 12:25, 19 October 2006 (BST)&lt;br /&gt;
&lt;br /&gt;
== Wiki Utillities ==&lt;br /&gt;
Utilities have been written to help the conversion of material from  HTML.&lt;br /&gt;
&lt;br /&gt;
# [http://diberri.dyndns.org/wikipedia/html2wiki/ A HTML2Wiki Converter]&lt;br /&gt;
&lt;br /&gt;
No wiki2html converter suitable for use has yet been identified.&lt;br /&gt;
=== Wiki Templates ===&lt;br /&gt;
&lt;br /&gt;
[[Template:DOI]] and [[Template:Doi-inline]] are providea as (protected) templates for your use.  Many other templates exist, often to be found on e.g. Wikipedia pages.  You may decide one of these is of particular use, or of interest.  If so, you can install it on the wiki here for you and others to use.  Add below a line that looks like  {{template-name|parameter}}, save, and click on the red text to create the new template. If you prefer the task of adding useful templates to that of adding information about molecules, then you will be given full credit for performing this valuable service for others!&lt;br /&gt;
--[[User:Rzepa|Rzepa]] 14:41, 20 October 2006 (BST)&lt;br /&gt;
&lt;br /&gt;
----&lt;br /&gt;
[[Template:Chem-Data]]&lt;/div&gt;</summary>
		<author><name>Jy405</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It:projects&amp;diff=4839</id>
		<title>It:projects</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It:projects&amp;diff=4839"/>
		<updated>2006-11-04T16:47:25Z</updated>

		<summary type="html">&lt;p&gt;Jy405: /* Supplemental  Project Page */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;__FORCETOC__&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;&#039;&#039;You MUST use the  Edit buttons on the right to edit this content.  Do NOT use the Edit button on the top of this page.&#039;&#039;&#039;&#039;&#039;&lt;br /&gt;
== Sandbox (Play-Pen) ==	 &lt;br /&gt;
		 &lt;br /&gt;
This is an area where you can play without worrying what you do. Enter it by pressing the [Edit] button &#039;&#039;&#039;on the right&#039;&#039;&#039; and &#039;&#039;&#039;not&#039;&#039;&#039; at the top. Go here for a [http://en.wikipedia.org/wiki/Wikipedia:Cheatsheet &#039;&#039;cheat sheet&#039;&#039;] summary of how to create a Wiki page.	 It&#039;s a free-for-all in here! Learn how to use a Wiki by coming here! PS This is how to do Greek: &amp;amp;Alpha;, &amp;amp;alpha;, &amp;amp;beta; &amp;amp;Delta;, &amp;amp;delta;	 		 &lt;br /&gt;
Try copying/pasting some of the [http://www.ch.ic.ac.uk/local/it/lab1.html examples in the course work] into this page. See the effect by selecting &#039;&#039;&#039;Show Preview&#039;&#039;&#039;. No not use &#039;&#039;&#039;Save Page&#039;&#039;&#039; so as to leave this area uncluttered for others.&lt;br /&gt;
----&lt;br /&gt;
&lt;br /&gt;
== Main Project Page ==&lt;br /&gt;
&#039;&#039;&#039;Please do not edit this page itself&#039;&#039;&#039;.  Click on one of the titles to start editing.&lt;br /&gt;
{| summary=&amp;quot;CIT Project  Titles&amp;quot; border=&amp;quot;1&amp;quot;&lt;br /&gt;
! bgcolor=&amp;quot;cyan&amp;quot; |Project&amp;lt;br /&amp;gt; Number&lt;br /&gt;
! bgcolor=&amp;quot;cyan&amp;quot; |General Keywords&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |01&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; | [[it:Lignocaine|Lignocaine (used in dentistry as a &amp;quot;local&amp;quot;)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |02&lt;br /&gt;
| bgcolor=&amp;quot;#66FF99&amp;quot; | [[it:Piperine|Piperine (active ingredient of both black and white pepper)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |03&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; | [[it:Rapamycin|Rapamycin (prevents transplant rejection)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |04&lt;br /&gt;
| bgcolor=&amp;quot;#66FF99&amp;quot; | [[it:Gossypol|Gossypol (male birth control)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |05&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; | [[it:Gentamycin|Gentamicin A (aminoglycoside antibiotic)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |06&lt;br /&gt;
| bgcolor=&amp;quot;#66FF99&amp;quot; | [[it:Herceptin|Herceptin (topical anticancer drug)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |07&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; | [[it:Gingerone|Zingerone (the characteristic smell of ginger)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |08&lt;br /&gt;
| bgcolor=&amp;quot;#66FF99&amp;quot; | [[it:Sucralose|Sucralose (non-metabolizable sweetening agent)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |09&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; | [[it:Bufotoxin|Bufotoxin (active component of the toad &#039;&#039;Bufo vulgaris&#039;&#039;)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |10&lt;br /&gt;
| bgcolor=&amp;quot;#66FF99&amp;quot; | [[it:Roaccutane|Roaccutane (treatment for severe acne)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |11&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; | [[it:Sibutramine|Sibutramine (appetite suppresor)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |12&lt;br /&gt;
| bgcolor=&amp;quot;#66FF99&amp;quot; | [[it:Anandamide|Anandamide (the &amp;quot;feel-good&amp;quot; factor in chocolate)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |13&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; | [[it:h3nbh3|Ammonia-borane: H&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;N-BH&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt; (Hydrogen storage molecule?)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |14&lt;br /&gt;
| bgcolor=&amp;quot;#66FF99&amp;quot; | [[it:Methoxsalen|Methoxsalen (Treatment of psoriasis)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |15&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; | [[it:Hycocine|Hyoscine (From Mandrake and Witches Henbane, pre-med before surgery)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |16&lt;br /&gt;
| bgcolor=&amp;quot;#66FF99&amp;quot; | [[it:Capreomycin|Capreomycin (Drug-resistant TB)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |17&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; | [[it:wilkinson|Wilkinson&#039;s catalyst]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |18&lt;br /&gt;
| bgcolor=&amp;quot;#66FF99&amp;quot; | [[it:Jacobsen|Jacobsen&#039;s epoxidation catalyst]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |19&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; | [[it:Methylaluminoxane|Methylaluminoxane: MAO - hugely important ethylene polymerisation cocatalyst]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |20&lt;br /&gt;
| bgcolor=&amp;quot;#66FF99&amp;quot; | [[it:Schwartz|Schwartz reagent for the hydrozirconation of alkenes and alkynes]]&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
== Supplemental  Project Page ==&lt;br /&gt;
&lt;br /&gt;
This area is for people who wish to create their own projects if none of the above appeal to them. Click on the  &#039;&#039;&#039;Edit&#039;&#039;&#039;  button to the right to open up an editable page,&lt;br /&gt;
then add an entry below as follows&lt;br /&gt;
&lt;br /&gt;
*&amp;lt;nowiki&amp;gt; [[it:name_of_project|Descriptive name of intended project]]&amp;lt;/nowiki&amp;gt;&lt;br /&gt;
*This will produce the effect:  [[it:name_of_project|Descriptive name of intended project]]&lt;br /&gt;
----&lt;br /&gt;
*[[it:sitagliptin_page|Sitagliptin]]&lt;br /&gt;
*[[it:Retinal|Retinal, molecule of sight]]&lt;br /&gt;
*[[it:Tamoxifen|Tamoxifen, breast cancer treatment]]&lt;br /&gt;
*[[it:Morphine|Morphine, painkiller]]&lt;br /&gt;
*[[it:Pelargonidin|Pelargonidin, colouring in nature]]&lt;br /&gt;
*[[it:Propanil|Propanil, weedkiller]]&lt;br /&gt;
*[[it:Ranitidine|Ranitidine, antiulcerative]]&lt;br /&gt;
*[[it:chlorphentermine|chlorphentermine, anorectic]]&lt;br /&gt;
*[[it:Serotonin|Serotonin, The &#039;HAPPY&#039; Drug]]&lt;br /&gt;
*[[it:Amphidinolide T1|Amphidinolide T1]]&lt;br /&gt;
*[[it:Rosiglitazone|Rosiglitazone, drug that is currently used to treat diabetes.]]&lt;br /&gt;
*[[it:Furosemide|Furosemide]]&lt;br /&gt;
*[[it:Tryptophan|Tryptophan]]&lt;br /&gt;
*[[it:methylpentynol|methylpentynol, tranquilliser.]]&lt;br /&gt;
*[[it:Ferrocene|Ferrocene]]&lt;br /&gt;
*[[it:Scopolamine|Scopolamine, the (Former) Truth Drug]]&lt;br /&gt;
*[[it:Camptothecin|Camptothecin,Anti-cancer agent ]]&lt;br /&gt;
*[[it:Salmeterol|Salmeterol, an agonist used to treat asthma]]&lt;br /&gt;
*[[it:Psilocin|Psilocin]]&lt;br /&gt;
*[[it:Epibatidine|Epibatidine]]&lt;br /&gt;
*[[it:Beta Carotene|Beta Carotene]]&lt;br /&gt;
*[[it:Thyroxine|Thyroxine, the Thyroid Hormone]]&lt;br /&gt;
*[[it:Tetrahydrocannabinol|Tetrahydrocannabinol]]&lt;br /&gt;
*[[it:Linalool|A component of essential oil]]&lt;br /&gt;
&lt;br /&gt;
== [[Special:Export|Export Pages]] ==&lt;br /&gt;
&lt;br /&gt;
== Overlaps ==&lt;br /&gt;
&lt;br /&gt;
If two people start editing a page at the same time, and  &#039;&#039;&#039;save&#039;&#039;&#039; the change simultaneously, its possible only one of the changes&lt;br /&gt;
will be made permanent.  If anyone spots this happening, please let  me know. &lt;br /&gt;
&lt;br /&gt;
One precaution you could take is to keep a copy of the contents of the page you are editing in eg Wordpad (or Word),&lt;br /&gt;
make the changes there, and then copy the entire lot to the  Wiki page to preview and then save. Tht way, if your contribution&lt;br /&gt;
is overlapped by someone else, you will still have a copy, and you can then resubmit it.&lt;br /&gt;
----&lt;br /&gt;
--[[User:Rzepa|Rzepa]] 12:25, 19 October 2006 (BST)&lt;br /&gt;
&lt;br /&gt;
== Wiki Utillities ==&lt;br /&gt;
Utilities have been written to help the conversion of material from  HTML.&lt;br /&gt;
&lt;br /&gt;
# [http://diberri.dyndns.org/wikipedia/html2wiki/ A HTML2Wiki Converter]&lt;br /&gt;
&lt;br /&gt;
No wiki2html converter suitable for use has yet been identified.&lt;br /&gt;
=== Wiki Templates ===&lt;br /&gt;
&lt;br /&gt;
[[Template:DOI]] and [[Template:Doi-inline]] are providea as (protected) templates for your use.  Many other templates exist, often to be found on e.g. Wikipedia pages.  You may decide one of these is of particular use, or of interest.  If so, you can install it on the wiki here for you and others to use.  Add below a line that looks like  {{template-name|parameter}}, save, and click on the red text to create the new template. If you prefer the task of adding useful templates to that of adding information about molecules, then you will be given full credit for performing this valuable service for others!&lt;br /&gt;
--[[User:Rzepa|Rzepa]] 14:41, 20 October 2006 (BST)&lt;br /&gt;
&lt;br /&gt;
----&lt;br /&gt;
[[Template:Chem-Data]]&lt;/div&gt;</summary>
		<author><name>Jy405</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It:projects&amp;diff=4838</id>
		<title>It:projects</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It:projects&amp;diff=4838"/>
		<updated>2006-11-04T16:44:08Z</updated>

		<summary type="html">&lt;p&gt;Jy405: /* Export Pages */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;__FORCETOC__&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;&#039;&#039;You MUST use the  Edit buttons on the right to edit this content.  Do NOT use the Edit button on the top of this page.&#039;&#039;&#039;&#039;&#039;&lt;br /&gt;
== Sandbox (Play-Pen) ==	 &lt;br /&gt;
		 &lt;br /&gt;
This is an area where you can play without worrying what you do. Enter it by pressing the [Edit] button &#039;&#039;&#039;on the right&#039;&#039;&#039; and &#039;&#039;&#039;not&#039;&#039;&#039; at the top. Go here for a [http://en.wikipedia.org/wiki/Wikipedia:Cheatsheet &#039;&#039;cheat sheet&#039;&#039;] summary of how to create a Wiki page.	 It&#039;s a free-for-all in here! Learn how to use a Wiki by coming here! PS This is how to do Greek: &amp;amp;Alpha;, &amp;amp;alpha;, &amp;amp;beta; &amp;amp;Delta;, &amp;amp;delta;	 		 &lt;br /&gt;
Try copying/pasting some of the [http://www.ch.ic.ac.uk/local/it/lab1.html examples in the course work] into this page. See the effect by selecting &#039;&#039;&#039;Show Preview&#039;&#039;&#039;. No not use &#039;&#039;&#039;Save Page&#039;&#039;&#039; so as to leave this area uncluttered for others.&lt;br /&gt;
----&lt;br /&gt;
&lt;br /&gt;
== Main Project Page ==&lt;br /&gt;
&#039;&#039;&#039;Please do not edit this page itself&#039;&#039;&#039;.  Click on one of the titles to start editing.&lt;br /&gt;
{| summary=&amp;quot;CIT Project  Titles&amp;quot; border=&amp;quot;1&amp;quot;&lt;br /&gt;
! bgcolor=&amp;quot;cyan&amp;quot; |Project&amp;lt;br /&amp;gt; Number&lt;br /&gt;
! bgcolor=&amp;quot;cyan&amp;quot; |General Keywords&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |01&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; | [[it:Lignocaine|Lignocaine (used in dentistry as a &amp;quot;local&amp;quot;)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |02&lt;br /&gt;
| bgcolor=&amp;quot;#66FF99&amp;quot; | [[it:Piperine|Piperine (active ingredient of both black and white pepper)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |03&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; | [[it:Rapamycin|Rapamycin (prevents transplant rejection)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |04&lt;br /&gt;
| bgcolor=&amp;quot;#66FF99&amp;quot; | [[it:Gossypol|Gossypol (male birth control)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |05&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; | [[it:Gentamycin|Gentamicin A (aminoglycoside antibiotic)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |06&lt;br /&gt;
| bgcolor=&amp;quot;#66FF99&amp;quot; | [[it:Herceptin|Herceptin (topical anticancer drug)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |07&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; | [[it:Gingerone|Zingerone (the characteristic smell of ginger)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |08&lt;br /&gt;
| bgcolor=&amp;quot;#66FF99&amp;quot; | [[it:Sucralose|Sucralose (non-metabolizable sweetening agent)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |09&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; | [[it:Bufotoxin|Bufotoxin (active component of the toad &#039;&#039;Bufo vulgaris&#039;&#039;)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |10&lt;br /&gt;
| bgcolor=&amp;quot;#66FF99&amp;quot; | [[it:Roaccutane|Roaccutane (treatment for severe acne)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |11&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; | [[it:Sibutramine|Sibutramine (appetite suppresor)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |12&lt;br /&gt;
| bgcolor=&amp;quot;#66FF99&amp;quot; | [[it:Anandamide|Anandamide (the &amp;quot;feel-good&amp;quot; factor in chocolate)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |13&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; | [[it:h3nbh3|Ammonia-borane: H&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;N-BH&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt; (Hydrogen storage molecule?)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |14&lt;br /&gt;
| bgcolor=&amp;quot;#66FF99&amp;quot; | [[it:Methoxsalen|Methoxsalen (Treatment of psoriasis)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |15&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; | [[it:Hycocine|Hyoscine (From Mandrake and Witches Henbane, pre-med before surgery)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |16&lt;br /&gt;
| bgcolor=&amp;quot;#66FF99&amp;quot; | [[it:Capreomycin|Capreomycin (Drug-resistant TB)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |17&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; | [[it:wilkinson|Wilkinson&#039;s catalyst]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |18&lt;br /&gt;
| bgcolor=&amp;quot;#66FF99&amp;quot; | [[it:Jacobsen|Jacobsen&#039;s epoxidation catalyst]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |19&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; | [[it:Methylaluminoxane|Methylaluminoxane: MAO - hugely important ethylene polymerisation cocatalyst]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |20&lt;br /&gt;
| bgcolor=&amp;quot;#66FF99&amp;quot; | [[it:Schwartz|Schwartz reagent for the hydrozirconation of alkenes and alkynes]]&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
== Supplemental  Project Page ==&lt;br /&gt;
&lt;br /&gt;
This area is for people who wish to create their own projects if none of the above appeal to them. Click on the  &#039;&#039;&#039;Edit&#039;&#039;&#039;  button to the right to open up an editable page,&lt;br /&gt;
then add an entry below as follows&lt;br /&gt;
&lt;br /&gt;
*&amp;lt;nowiki&amp;gt; [[it:name_of_project|Descriptive name of intended project]]&amp;lt;/nowiki&amp;gt;&lt;br /&gt;
*This will produce the effect:  [[it:name_of_project|Descriptive name of intended project]]&lt;br /&gt;
----&lt;br /&gt;
*[[it:sitagliptin_page|Sitagliptin]]&lt;br /&gt;
*[[it:Retinal|Retinal, molecule of sight]]&lt;br /&gt;
*[[it:Tamoxifen|Tamoxifen, breast cancer treatment]]&lt;br /&gt;
*[[it:Morphine|Morphine, painkiller]]&lt;br /&gt;
*[[it:Pelargonidin|Pelargonidin, colouring in nature]]&lt;br /&gt;
*[[it:Propanil|Propanil, weedkiller]]&lt;br /&gt;
*[[it:Ranitidine|Ranitidine, antiulcerative]]&lt;br /&gt;
*[[it:chlorphentermine|chlorphentermine, anorectic]]&lt;br /&gt;
*[[it:Serotonin|Serotonin, The &#039;HAPPY&#039; Drug]]&lt;br /&gt;
*[[it:Amphidinolide T1|Amphidinolide T1]]&lt;br /&gt;
*[[it:Rosiglitazone|Rosiglitazone, drug that is currently used to treat diabetes.]]&lt;br /&gt;
*[[it:Furosemide|Furosemide]]&lt;br /&gt;
*[[it:Tryptophan|Tryptophan]]&lt;br /&gt;
*[[it:methylpentynol|methylpentynol, tranquilliser.]]&lt;br /&gt;
*[[it:Ferrocene|Ferrocene]]&lt;br /&gt;
*[[it:Scopolamine|Scopolamine, the (Former) Truth Drug]]&lt;br /&gt;
*[[it:Camptothecin|Camptothecin,Anti-cancer agent ]]&lt;br /&gt;
*[[it:Salmeterol|Salmeterol, an agonist used to treat asthma]]&lt;br /&gt;
*[[it:Psilocin|Psilocin]]&lt;br /&gt;
*[[it:Epibatidine|Epibatidine]]&lt;br /&gt;
*[[it:Beta Carotene|Beta Carotene]]&lt;br /&gt;
*[[it:Thyroxine|Thyroxine, the Thyroid Hormone]]&lt;br /&gt;
*[[it:Tetrahydrocannabinol|Tetrahydrocannabinol]]&lt;br /&gt;
&lt;br /&gt;
== [[Special:Export|Export Pages]] ==&lt;br /&gt;
&lt;br /&gt;
== Overlaps ==&lt;br /&gt;
&lt;br /&gt;
If two people start editing a page at the same time, and  &#039;&#039;&#039;save&#039;&#039;&#039; the change simultaneously, its possible only one of the changes&lt;br /&gt;
will be made permanent.  If anyone spots this happening, please let  me know. &lt;br /&gt;
&lt;br /&gt;
One precaution you could take is to keep a copy of the contents of the page you are editing in eg Wordpad (or Word),&lt;br /&gt;
make the changes there, and then copy the entire lot to the  Wiki page to preview and then save. Tht way, if your contribution&lt;br /&gt;
is overlapped by someone else, you will still have a copy, and you can then resubmit it.&lt;br /&gt;
----&lt;br /&gt;
--[[User:Rzepa|Rzepa]] 12:25, 19 October 2006 (BST)&lt;br /&gt;
&lt;br /&gt;
== Wiki Utillities ==&lt;br /&gt;
Utilities have been written to help the conversion of material from  HTML.&lt;br /&gt;
&lt;br /&gt;
# [http://diberri.dyndns.org/wikipedia/html2wiki/ A HTML2Wiki Converter]&lt;br /&gt;
&lt;br /&gt;
No wiki2html converter suitable for use has yet been identified.&lt;br /&gt;
=== Wiki Templates ===&lt;br /&gt;
&lt;br /&gt;
[[Template:DOI]] and [[Template:Doi-inline]] are providea as (protected) templates for your use.  Many other templates exist, often to be found on e.g. Wikipedia pages.  You may decide one of these is of particular use, or of interest.  If so, you can install it on the wiki here for you and others to use.  Add below a line that looks like  {{template-name|parameter}}, save, and click on the red text to create the new template. If you prefer the task of adding useful templates to that of adding information about molecules, then you will be given full credit for performing this valuable service for others!&lt;br /&gt;
--[[User:Rzepa|Rzepa]] 14:41, 20 October 2006 (BST)&lt;br /&gt;
&lt;br /&gt;
----&lt;br /&gt;
[[Template:Chem-Data]]&lt;/div&gt;</summary>
		<author><name>Jy405</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It:projects&amp;diff=4837</id>
		<title>It:projects</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It:projects&amp;diff=4837"/>
		<updated>2006-11-04T16:39:58Z</updated>

		<summary type="html">&lt;p&gt;Jy405: /* Export Pages */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;__FORCETOC__&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;&#039;&#039;You MUST use the  Edit buttons on the right to edit this content.  Do NOT use the Edit button on the top of this page.&#039;&#039;&#039;&#039;&#039;&lt;br /&gt;
== Sandbox (Play-Pen) ==	 &lt;br /&gt;
		 &lt;br /&gt;
This is an area where you can play without worrying what you do. Enter it by pressing the [Edit] button &#039;&#039;&#039;on the right&#039;&#039;&#039; and &#039;&#039;&#039;not&#039;&#039;&#039; at the top. Go here for a [http://en.wikipedia.org/wiki/Wikipedia:Cheatsheet &#039;&#039;cheat sheet&#039;&#039;] summary of how to create a Wiki page.	 It&#039;s a free-for-all in here! Learn how to use a Wiki by coming here! PS This is how to do Greek: &amp;amp;Alpha;, &amp;amp;alpha;, &amp;amp;beta; &amp;amp;Delta;, &amp;amp;delta;	 		 &lt;br /&gt;
Try copying/pasting some of the [http://www.ch.ic.ac.uk/local/it/lab1.html examples in the course work] into this page. See the effect by selecting &#039;&#039;&#039;Show Preview&#039;&#039;&#039;. No not use &#039;&#039;&#039;Save Page&#039;&#039;&#039; so as to leave this area uncluttered for others.&lt;br /&gt;
----&lt;br /&gt;
&lt;br /&gt;
== Main Project Page ==&lt;br /&gt;
&#039;&#039;&#039;Please do not edit this page itself&#039;&#039;&#039;.  Click on one of the titles to start editing.&lt;br /&gt;
{| summary=&amp;quot;CIT Project  Titles&amp;quot; border=&amp;quot;1&amp;quot;&lt;br /&gt;
! bgcolor=&amp;quot;cyan&amp;quot; |Project&amp;lt;br /&amp;gt; Number&lt;br /&gt;
! bgcolor=&amp;quot;cyan&amp;quot; |General Keywords&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |01&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; | [[it:Lignocaine|Lignocaine (used in dentistry as a &amp;quot;local&amp;quot;)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |02&lt;br /&gt;
| bgcolor=&amp;quot;#66FF99&amp;quot; | [[it:Piperine|Piperine (active ingredient of both black and white pepper)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |03&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; | [[it:Rapamycin|Rapamycin (prevents transplant rejection)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |04&lt;br /&gt;
| bgcolor=&amp;quot;#66FF99&amp;quot; | [[it:Gossypol|Gossypol (male birth control)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |05&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; | [[it:Gentamycin|Gentamicin A (aminoglycoside antibiotic)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |06&lt;br /&gt;
| bgcolor=&amp;quot;#66FF99&amp;quot; | [[it:Herceptin|Herceptin (topical anticancer drug)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |07&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; | [[it:Gingerone|Zingerone (the characteristic smell of ginger)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |08&lt;br /&gt;
| bgcolor=&amp;quot;#66FF99&amp;quot; | [[it:Sucralose|Sucralose (non-metabolizable sweetening agent)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |09&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; | [[it:Bufotoxin|Bufotoxin (active component of the toad &#039;&#039;Bufo vulgaris&#039;&#039;)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |10&lt;br /&gt;
| bgcolor=&amp;quot;#66FF99&amp;quot; | [[it:Roaccutane|Roaccutane (treatment for severe acne)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |11&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; | [[it:Sibutramine|Sibutramine (appetite suppresor)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |12&lt;br /&gt;
| bgcolor=&amp;quot;#66FF99&amp;quot; | [[it:Anandamide|Anandamide (the &amp;quot;feel-good&amp;quot; factor in chocolate)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |13&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; | [[it:h3nbh3|Ammonia-borane: H&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;N-BH&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt; (Hydrogen storage molecule?)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |14&lt;br /&gt;
| bgcolor=&amp;quot;#66FF99&amp;quot; | [[it:Methoxsalen|Methoxsalen (Treatment of psoriasis)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |15&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; | [[it:Hycocine|Hyoscine (From Mandrake and Witches Henbane, pre-med before surgery)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |16&lt;br /&gt;
| bgcolor=&amp;quot;#66FF99&amp;quot; | [[it:Capreomycin|Capreomycin (Drug-resistant TB)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |17&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; | [[it:wilkinson|Wilkinson&#039;s catalyst]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |18&lt;br /&gt;
| bgcolor=&amp;quot;#66FF99&amp;quot; | [[it:Jacobsen|Jacobsen&#039;s epoxidation catalyst]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |19&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; | [[it:Methylaluminoxane|Methylaluminoxane: MAO - hugely important ethylene polymerisation cocatalyst]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |20&lt;br /&gt;
| bgcolor=&amp;quot;#66FF99&amp;quot; | [[it:Schwartz|Schwartz reagent for the hydrozirconation of alkenes and alkynes]]&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
== Supplemental  Project Page ==&lt;br /&gt;
&lt;br /&gt;
This area is for people who wish to create their own projects if none of the above appeal to them. Click on the  &#039;&#039;&#039;Edit&#039;&#039;&#039;  button to the right to open up an editable page,&lt;br /&gt;
then add an entry below as follows&lt;br /&gt;
&lt;br /&gt;
*&amp;lt;nowiki&amp;gt; [[it:name_of_project|Descriptive name of intended project]]&amp;lt;/nowiki&amp;gt;&lt;br /&gt;
*This will produce the effect:  [[it:name_of_project|Descriptive name of intended project]]&lt;br /&gt;
----&lt;br /&gt;
*[[it:sitagliptin_page|Sitagliptin]]&lt;br /&gt;
*[[it:Retinal|Retinal, molecule of sight]]&lt;br /&gt;
*[[it:Tamoxifen|Tamoxifen, breast cancer treatment]]&lt;br /&gt;
*[[it:Morphine|Morphine, painkiller]]&lt;br /&gt;
*[[it:Pelargonidin|Pelargonidin, colouring in nature]]&lt;br /&gt;
*[[it:Propanil|Propanil, weedkiller]]&lt;br /&gt;
*[[it:Ranitidine|Ranitidine, antiulcerative]]&lt;br /&gt;
*[[it:chlorphentermine|chlorphentermine, anorectic]]&lt;br /&gt;
*[[it:Serotonin|Serotonin, The &#039;HAPPY&#039; Drug]]&lt;br /&gt;
*[[it:Amphidinolide T1|Amphidinolide T1]]&lt;br /&gt;
*[[it:Rosiglitazone|Rosiglitazone, drug that is currently used to treat diabetes.]]&lt;br /&gt;
*[[it:Furosemide|Furosemide]]&lt;br /&gt;
*[[it:Tryptophan|Tryptophan]]&lt;br /&gt;
*[[it:methylpentynol|methylpentynol, tranquilliser.]]&lt;br /&gt;
*[[it:Ferrocene|Ferrocene]]&lt;br /&gt;
*[[it:Scopolamine|Scopolamine, the (Former) Truth Drug]]&lt;br /&gt;
*[[it:Camptothecin|Camptothecin,Anti-cancer agent ]]&lt;br /&gt;
*[[it:Salmeterol|Salmeterol, an agonist used to treat asthma]]&lt;br /&gt;
*[[it:Psilocin|Psilocin]]&lt;br /&gt;
*[[it:Epibatidine|Epibatidine]]&lt;br /&gt;
*[[it:Beta Carotene|Beta Carotene]]&lt;br /&gt;
*[[it:Thyroxine|Thyroxine, the Thyroid Hormone]]&lt;br /&gt;
*[[it:Tetrahydrocannabinol|Tetrahydrocannabinol]]&lt;br /&gt;
&lt;br /&gt;
== [[Special:Export|Export Pages]] ==&lt;br /&gt;
&lt;br /&gt;
[[it:name_of_project| Linalool(A component in essential oil)]]&lt;br /&gt;
&lt;br /&gt;
Introduction&lt;br /&gt;
Lavender is a shrubby plant in the mint family with about 25-30 species. It is native from the Mediterranean region south to tropical Afric and the east to India. The aromatic smell is found in all parts of the shrub, but the essential oil is only produced from the flowers and flower-stalks. The lavender flower oil is a complex mixture compounds containing linalool, linalyl acetate, 1, 8-cineole, β-ocimene and so on.&lt;br /&gt;
 &lt;br /&gt;
Linalool is a colourless fragrant liquid which can be found in many essential oil.&lt;br /&gt;
&lt;br /&gt;
== Overlaps ==&lt;br /&gt;
&lt;br /&gt;
If two people start editing a page at the same time, and  &#039;&#039;&#039;save&#039;&#039;&#039; the change simultaneously, its possible only one of the changes&lt;br /&gt;
will be made permanent.  If anyone spots this happening, please let  me know. &lt;br /&gt;
&lt;br /&gt;
One precaution you could take is to keep a copy of the contents of the page you are editing in eg Wordpad (or Word),&lt;br /&gt;
make the changes there, and then copy the entire lot to the  Wiki page to preview and then save. Tht way, if your contribution&lt;br /&gt;
is overlapped by someone else, you will still have a copy, and you can then resubmit it.&lt;br /&gt;
----&lt;br /&gt;
--[[User:Rzepa|Rzepa]] 12:25, 19 October 2006 (BST)&lt;br /&gt;
&lt;br /&gt;
== Wiki Utillities ==&lt;br /&gt;
Utilities have been written to help the conversion of material from  HTML.&lt;br /&gt;
&lt;br /&gt;
# [http://diberri.dyndns.org/wikipedia/html2wiki/ A HTML2Wiki Converter]&lt;br /&gt;
&lt;br /&gt;
No wiki2html converter suitable for use has yet been identified.&lt;br /&gt;
=== Wiki Templates ===&lt;br /&gt;
&lt;br /&gt;
[[Template:DOI]] and [[Template:Doi-inline]] are providea as (protected) templates for your use.  Many other templates exist, often to be found on e.g. Wikipedia pages.  You may decide one of these is of particular use, or of interest.  If so, you can install it on the wiki here for you and others to use.  Add below a line that looks like  {{template-name|parameter}}, save, and click on the red text to create the new template. If you prefer the task of adding useful templates to that of adding information about molecules, then you will be given full credit for performing this valuable service for others!&lt;br /&gt;
--[[User:Rzepa|Rzepa]] 14:41, 20 October 2006 (BST)&lt;br /&gt;
&lt;br /&gt;
----&lt;br /&gt;
[[Template:Chem-Data]]&lt;/div&gt;</summary>
		<author><name>Jy405</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It:projects&amp;diff=4836</id>
		<title>It:projects</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It:projects&amp;diff=4836"/>
		<updated>2006-11-04T16:34:14Z</updated>

		<summary type="html">&lt;p&gt;Jy405: /* Export Pages */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;__FORCETOC__&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;&#039;&#039;You MUST use the  Edit buttons on the right to edit this content.  Do NOT use the Edit button on the top of this page.&#039;&#039;&#039;&#039;&#039;&lt;br /&gt;
== Sandbox (Play-Pen) ==	 &lt;br /&gt;
		 &lt;br /&gt;
This is an area where you can play without worrying what you do. Enter it by pressing the [Edit] button &#039;&#039;&#039;on the right&#039;&#039;&#039; and &#039;&#039;&#039;not&#039;&#039;&#039; at the top. Go here for a [http://en.wikipedia.org/wiki/Wikipedia:Cheatsheet &#039;&#039;cheat sheet&#039;&#039;] summary of how to create a Wiki page.	 It&#039;s a free-for-all in here! Learn how to use a Wiki by coming here! PS This is how to do Greek: &amp;amp;Alpha;, &amp;amp;alpha;, &amp;amp;beta; &amp;amp;Delta;, &amp;amp;delta;	 		 &lt;br /&gt;
Try copying/pasting some of the [http://www.ch.ic.ac.uk/local/it/lab1.html examples in the course work] into this page. See the effect by selecting &#039;&#039;&#039;Show Preview&#039;&#039;&#039;. No not use &#039;&#039;&#039;Save Page&#039;&#039;&#039; so as to leave this area uncluttered for others.&lt;br /&gt;
----&lt;br /&gt;
&lt;br /&gt;
== Main Project Page ==&lt;br /&gt;
&#039;&#039;&#039;Please do not edit this page itself&#039;&#039;&#039;.  Click on one of the titles to start editing.&lt;br /&gt;
{| summary=&amp;quot;CIT Project  Titles&amp;quot; border=&amp;quot;1&amp;quot;&lt;br /&gt;
! bgcolor=&amp;quot;cyan&amp;quot; |Project&amp;lt;br /&amp;gt; Number&lt;br /&gt;
! bgcolor=&amp;quot;cyan&amp;quot; |General Keywords&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |01&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; | [[it:Lignocaine|Lignocaine (used in dentistry as a &amp;quot;local&amp;quot;)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |02&lt;br /&gt;
| bgcolor=&amp;quot;#66FF99&amp;quot; | [[it:Piperine|Piperine (active ingredient of both black and white pepper)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |03&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; | [[it:Rapamycin|Rapamycin (prevents transplant rejection)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |04&lt;br /&gt;
| bgcolor=&amp;quot;#66FF99&amp;quot; | [[it:Gossypol|Gossypol (male birth control)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |05&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; | [[it:Gentamycin|Gentamicin A (aminoglycoside antibiotic)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |06&lt;br /&gt;
| bgcolor=&amp;quot;#66FF99&amp;quot; | [[it:Herceptin|Herceptin (topical anticancer drug)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |07&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; | [[it:Gingerone|Zingerone (the characteristic smell of ginger)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |08&lt;br /&gt;
| bgcolor=&amp;quot;#66FF99&amp;quot; | [[it:Sucralose|Sucralose (non-metabolizable sweetening agent)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |09&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; | [[it:Bufotoxin|Bufotoxin (active component of the toad &#039;&#039;Bufo vulgaris&#039;&#039;)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |10&lt;br /&gt;
| bgcolor=&amp;quot;#66FF99&amp;quot; | [[it:Roaccutane|Roaccutane (treatment for severe acne)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |11&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; | [[it:Sibutramine|Sibutramine (appetite suppresor)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |12&lt;br /&gt;
| bgcolor=&amp;quot;#66FF99&amp;quot; | [[it:Anandamide|Anandamide (the &amp;quot;feel-good&amp;quot; factor in chocolate)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |13&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; | [[it:h3nbh3|Ammonia-borane: H&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;N-BH&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt; (Hydrogen storage molecule?)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |14&lt;br /&gt;
| bgcolor=&amp;quot;#66FF99&amp;quot; | [[it:Methoxsalen|Methoxsalen (Treatment of psoriasis)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |15&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; | [[it:Hycocine|Hyoscine (From Mandrake and Witches Henbane, pre-med before surgery)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |16&lt;br /&gt;
| bgcolor=&amp;quot;#66FF99&amp;quot; | [[it:Capreomycin|Capreomycin (Drug-resistant TB)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |17&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; | [[it:wilkinson|Wilkinson&#039;s catalyst]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |18&lt;br /&gt;
| bgcolor=&amp;quot;#66FF99&amp;quot; | [[it:Jacobsen|Jacobsen&#039;s epoxidation catalyst]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |19&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; | [[it:Methylaluminoxane|Methylaluminoxane: MAO - hugely important ethylene polymerisation cocatalyst]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |20&lt;br /&gt;
| bgcolor=&amp;quot;#66FF99&amp;quot; | [[it:Schwartz|Schwartz reagent for the hydrozirconation of alkenes and alkynes]]&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
== Supplemental  Project Page ==&lt;br /&gt;
&lt;br /&gt;
This area is for people who wish to create their own projects if none of the above appeal to them. Click on the  &#039;&#039;&#039;Edit&#039;&#039;&#039;  button to the right to open up an editable page,&lt;br /&gt;
then add an entry below as follows&lt;br /&gt;
&lt;br /&gt;
*&amp;lt;nowiki&amp;gt; [[it:name_of_project|Descriptive name of intended project]]&amp;lt;/nowiki&amp;gt;&lt;br /&gt;
*This will produce the effect:  [[it:name_of_project|Descriptive name of intended project]]&lt;br /&gt;
----&lt;br /&gt;
*[[it:sitagliptin_page|Sitagliptin]]&lt;br /&gt;
*[[it:Retinal|Retinal, molecule of sight]]&lt;br /&gt;
*[[it:Tamoxifen|Tamoxifen, breast cancer treatment]]&lt;br /&gt;
*[[it:Morphine|Morphine, painkiller]]&lt;br /&gt;
*[[it:Pelargonidin|Pelargonidin, colouring in nature]]&lt;br /&gt;
*[[it:Propanil|Propanil, weedkiller]]&lt;br /&gt;
*[[it:Ranitidine|Ranitidine, antiulcerative]]&lt;br /&gt;
*[[it:chlorphentermine|chlorphentermine, anorectic]]&lt;br /&gt;
*[[it:Serotonin|Serotonin, The &#039;HAPPY&#039; Drug]]&lt;br /&gt;
*[[it:Amphidinolide T1|Amphidinolide T1]]&lt;br /&gt;
*[[it:Rosiglitazone|Rosiglitazone, drug that is currently used to treat diabetes.]]&lt;br /&gt;
*[[it:Furosemide|Furosemide]]&lt;br /&gt;
*[[it:Tryptophan|Tryptophan]]&lt;br /&gt;
*[[it:methylpentynol|methylpentynol, tranquilliser.]]&lt;br /&gt;
*[[it:Ferrocene|Ferrocene]]&lt;br /&gt;
*[[it:Scopolamine|Scopolamine, the (Former) Truth Drug]]&lt;br /&gt;
*[[it:Camptothecin|Camptothecin,Anti-cancer agent ]]&lt;br /&gt;
*[[it:Salmeterol|Salmeterol, an agonist used to treat asthma]]&lt;br /&gt;
*[[it:Psilocin|Psilocin]]&lt;br /&gt;
*[[it:Epibatidine|Epibatidine]]&lt;br /&gt;
*[[it:Beta Carotene|Beta Carotene]]&lt;br /&gt;
*[[it:Thyroxine|Thyroxine, the Thyroid Hormone]]&lt;br /&gt;
*[[it:Tetrahydrocannabinol|Tetrahydrocannabinol]]&lt;br /&gt;
&lt;br /&gt;
== [[Special:Export|Export Pages]] ==&lt;br /&gt;
&lt;br /&gt;
[[it:name_of_project| Linalool(A component in essential oil)]]&lt;br /&gt;
&lt;br /&gt;
== Overlaps ==&lt;br /&gt;
&lt;br /&gt;
If two people start editing a page at the same time, and  &#039;&#039;&#039;save&#039;&#039;&#039; the change simultaneously, its possible only one of the changes&lt;br /&gt;
will be made permanent.  If anyone spots this happening, please let  me know. &lt;br /&gt;
&lt;br /&gt;
One precaution you could take is to keep a copy of the contents of the page you are editing in eg Wordpad (or Word),&lt;br /&gt;
make the changes there, and then copy the entire lot to the  Wiki page to preview and then save. Tht way, if your contribution&lt;br /&gt;
is overlapped by someone else, you will still have a copy, and you can then resubmit it.&lt;br /&gt;
----&lt;br /&gt;
--[[User:Rzepa|Rzepa]] 12:25, 19 October 2006 (BST)&lt;br /&gt;
&lt;br /&gt;
== Wiki Utillities ==&lt;br /&gt;
Utilities have been written to help the conversion of material from  HTML.&lt;br /&gt;
&lt;br /&gt;
# [http://diberri.dyndns.org/wikipedia/html2wiki/ A HTML2Wiki Converter]&lt;br /&gt;
&lt;br /&gt;
No wiki2html converter suitable for use has yet been identified.&lt;br /&gt;
=== Wiki Templates ===&lt;br /&gt;
&lt;br /&gt;
[[Template:DOI]] and [[Template:Doi-inline]] are providea as (protected) templates for your use.  Many other templates exist, often to be found on e.g. Wikipedia pages.  You may decide one of these is of particular use, or of interest.  If so, you can install it on the wiki here for you and others to use.  Add below a line that looks like  {{template-name|parameter}}, save, and click on the red text to create the new template. If you prefer the task of adding useful templates to that of adding information about molecules, then you will be given full credit for performing this valuable service for others!&lt;br /&gt;
--[[User:Rzepa|Rzepa]] 14:41, 20 October 2006 (BST)&lt;br /&gt;
&lt;br /&gt;
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[[Template:Chem-Data]]&lt;/div&gt;</summary>
		<author><name>Jy405</name></author>
	</entry>
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