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	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It:MSG&amp;diff=5525</id>
		<title>It:MSG</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It:MSG&amp;diff=5525"/>
		<updated>2006-11-20T10:57:35Z</updated>

		<summary type="html">&lt;p&gt;Rw305: /* References &amp;amp; Useful Links */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;==Abstract==&lt;br /&gt;
[[Image:msg2.bmp|centre|300px|Chemical Structure of MSG]]&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;Monosodium Glutamate&#039;&#039;&#039; is more commonly known as &#039;&#039;&#039;MSG&#039;&#039;&#039; and has become the choice chemical for the enhancement of flavour in many foods. It was originally discovered in 1909 by the Ajinomoto Corporation in Japan.&lt;br /&gt;
&lt;br /&gt;
==The Basics==&lt;br /&gt;
{| class=&amp;quot;toccolours&amp;quot; border=&amp;quot;1&amp;quot; style=&amp;quot;float: right; clear: right; margin: 0 0 1em 1em; border-collapse: collapse;&amp;quot;&lt;br /&gt;
! {{chembox header}} | MSG &lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; width=&amp;quot;300&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image:msg.jpg]]&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | General&lt;br /&gt;
|-&lt;br /&gt;
| IUPAC nomenclature|Systematic name&lt;br /&gt;
|2-aminopentanedioic acid&lt;br /&gt;
|-&lt;br /&gt;
| Other names&lt;br /&gt;
|2-aminoglutaric acid, 1-aminopropane-1,&lt;br /&gt;
3-dicarboxylic acid&lt;br /&gt;
|-&lt;br /&gt;
| Chemical formula|Molecular formula]&lt;br /&gt;
|C&amp;lt;sub&amp;gt;5&amp;lt;/sub&amp;gt;H&amp;lt;sub&amp;gt;8&amp;lt;/sub&amp;gt;NNaO&amp;lt;sub&amp;gt;4&amp;lt;/sub&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
|-&lt;br /&gt;
| Molecular Weight&lt;br /&gt;
| 169.11&lt;br /&gt;
|-&lt;br /&gt;
| Appearance&lt;br /&gt;
| White Crystalline Solid&lt;br /&gt;
|-&lt;br /&gt;
| CAS registry number|CAS number&lt;br /&gt;
|142-47-2&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Properties&lt;br /&gt;
|-&lt;br /&gt;
| Melting point&lt;br /&gt;
| 232 °C (505 K)&lt;br /&gt;
|-&lt;br /&gt;
| Related compounds &lt;br /&gt;
| Glutamic Acid&lt;br /&gt;
|-&lt;br /&gt;
| Solubility in Water&lt;br /&gt;
| 100 mg/100ml&lt;br /&gt;
|-&lt;br /&gt;
| pH&lt;br /&gt;
| 7.0&lt;br /&gt;
|-&lt;br /&gt;
| {{chembox header}} | &amp;lt;small&amp;gt;Except where noted otherwise, data are given for&amp;lt;br /&amp;gt; materials in their [[standard state|standard state (at 25&amp;amp;nbsp;°C, 100&amp;amp;nbsp;kPa)]]&amp;lt;br /&amp;gt;[[wikipedia:Chemical infobox|Infobox disclaimer and references]]&amp;lt;/small&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
|}&lt;br /&gt;
MSG,is a sodium salt of the amino acid &#039;&#039;&#039;&#039;&#039;L-glutamic acid&#039;&#039;&#039;&#039;&#039;. It is practically odorless. It is produced by a bacterial fermentation process with starch or molasses as carbon sources and ammonium salts as nitrogen sources (Steffen process). MSG is not a direct taste enhancer but a complex flavour enhancer for gravies, meats, poultry, sauces, and in other combinations. It is also used to enhance the taste of tobacco and has been used medically to treat hepatic coma.&lt;br /&gt;
&lt;br /&gt;
===3D Representation===&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;green&amp;lt;/color&amp;gt;&lt;br /&gt;
&amp;lt;script&amp;gt;zoom 150; 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;&lt;br /&gt;
HEADER    NONAME 16-Nov-06                                              NONE   1&lt;br /&gt;
TITLE                                                                   NONE   2&lt;br /&gt;
AUTHOR    WWW daemon apache                                             NONE   3&lt;br /&gt;
REVDAT   1  16-Nov-06     0                                             NONE   4&lt;br /&gt;
ATOM      1  O           0       3.779  -0.333   0.251  0.00  0.00           O+0&lt;br /&gt;
ATOM      2  C           0       2.568   0.160  -0.050  0.00  0.00           C+0&lt;br /&gt;
ATOM      3  C           0       1.326  -0.540   0.437  0.00  0.00           C+0&lt;br /&gt;
ATOM      4  C           0       0.089   0.222  -0.042  0.00  0.00           C+0&lt;br /&gt;
ATOM      5  C           0      -1.172  -0.489   0.453  0.00  0.00           C+0&lt;br /&gt;
ATOM      6  H           0      -1.124  -0.603   1.536  0.00  0.00           H+0&lt;br /&gt;
ATOM      7  N           0      -1.265  -1.814  -0.174  0.00  0.00           N+0&lt;br /&gt;
ATOM      8  C           0      -2.385   0.327   0.088  0.00  0.00           C+0&lt;br /&gt;
ATOM      9  O           0      -3.155  -0.075  -0.769  0.00  0.00           O-1&lt;br /&gt;
ATOM     10  O           0      -2.598   1.389   0.648  0.00  0.00           O+0&lt;br /&gt;
ATOM     11  O           0       2.473   1.167  -0.713  0.00  0.00           O+0&lt;br /&gt;
ATOM     12  H           0       4.576   0.116  -0.061  0.00  0.00           H+0&lt;br /&gt;
ATOM     13  H           0       1.302  -1.556   0.041  0.00  0.00           H+0&lt;br /&gt;
ATOM     14  H           0       1.332  -0.575   1.527  0.00  0.00           H+0&lt;br /&gt;
ATOM     15  H           0       0.112   1.238   0.354  0.00  0.00           H+0&lt;br /&gt;
ATOM     16  H           0       0.083   0.257  -1.131  0.00  0.00           H+0&lt;br /&gt;
ATOM     17  H           0      -1.307  -1.660  -1.171  0.00  0.00           H+0&lt;br /&gt;
ATOM     18  H           0      -0.392  -2.284   0.010  0.00  0.00           H+0&lt;br /&gt;
CONECT    1    2   12    0    0                                         NONE  23&lt;br /&gt;
CONECT    2    1    3   11    0                                         NONE  24&lt;br /&gt;
CONECT    3    2    4   13   14                                         NONE  25&lt;br /&gt;
CONECT    4    3    5   15   16                                         NONE  26&lt;br /&gt;
CONECT    5    4    6    7    8                                         NONE  27&lt;br /&gt;
CONECT    7    5   17   18    0                                         NONE  28&lt;br /&gt;
CONECT    8    5    9   10    0                                         NONE  29&lt;br /&gt;
CONECT    9    8    0    0    0                                         NONE  30&lt;br /&gt;
CONECT   10    8    0    0    0                                         NONE  31&lt;br /&gt;
CONECT   11    2    0    0    0                                         NONE  32&lt;br /&gt;
END                                                                     NONE  33&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;
&lt;br /&gt;
&lt;br /&gt;
===Spectra===&lt;br /&gt;
[[Image:NMR of MSG.bmp|600px|&amp;lt;sup&amp;gt;1&amp;lt;/sup&amp;gt;H NMR Spectrum of MSG]]&lt;br /&gt;
&lt;br /&gt;
===Source &amp;amp; Manufacturing===&lt;br /&gt;
Glutamate itself is a naturally occuring amino acid that can be found in human bodies and high-protein foods (eg. nuts, meats and most dairy products). When it is not bound to sodium some of the glutamate is in the &amp;quot;free&amp;quot; ionic form; and only this free form of glutamate can enhance the flavor of foods. Tomatoes also have a high concentration of the free glutamate form making them natural flavour enhancers.&lt;br /&gt;
&lt;br /&gt;
Originally extracted from seaweed, modern MSG is produced by the fermentation of starch, sugar beets, sugar cane, or molasses.&lt;br /&gt;
&lt;br /&gt;
==References &amp;amp; Useful Links==&lt;br /&gt;
Image: http://www.germes-online.com/catalog/48/55/189/257161/monosodium_glutamate.html&lt;br /&gt;
&lt;br /&gt;
http://www.chemicalland21.com/lifescience/foco/MONOSODIUM%20GLUTAMATE.htm&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
--[[User:Rw305|Rw305]] 10:57, 20 November 2006 (UTC)&lt;/div&gt;</summary>
		<author><name>Rw305</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It:MSG&amp;diff=5524</id>
		<title>It:MSG</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It:MSG&amp;diff=5524"/>
		<updated>2006-11-20T10:57:10Z</updated>

		<summary type="html">&lt;p&gt;Rw305: /* Source &amp;amp; Manufacturing */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;==Abstract==&lt;br /&gt;
[[Image:msg2.bmp|centre|300px|Chemical Structure of MSG]]&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;Monosodium Glutamate&#039;&#039;&#039; is more commonly known as &#039;&#039;&#039;MSG&#039;&#039;&#039; and has become the choice chemical for the enhancement of flavour in many foods. It was originally discovered in 1909 by the Ajinomoto Corporation in Japan.&lt;br /&gt;
&lt;br /&gt;
==The Basics==&lt;br /&gt;
{| class=&amp;quot;toccolours&amp;quot; border=&amp;quot;1&amp;quot; style=&amp;quot;float: right; clear: right; margin: 0 0 1em 1em; border-collapse: collapse;&amp;quot;&lt;br /&gt;
! {{chembox header}} | MSG &lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; width=&amp;quot;300&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image:msg.jpg]]&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | General&lt;br /&gt;
|-&lt;br /&gt;
| IUPAC nomenclature|Systematic name&lt;br /&gt;
|2-aminopentanedioic acid&lt;br /&gt;
|-&lt;br /&gt;
| Other names&lt;br /&gt;
|2-aminoglutaric acid, 1-aminopropane-1,&lt;br /&gt;
3-dicarboxylic acid&lt;br /&gt;
|-&lt;br /&gt;
| Chemical formula|Molecular formula]&lt;br /&gt;
|C&amp;lt;sub&amp;gt;5&amp;lt;/sub&amp;gt;H&amp;lt;sub&amp;gt;8&amp;lt;/sub&amp;gt;NNaO&amp;lt;sub&amp;gt;4&amp;lt;/sub&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
|-&lt;br /&gt;
| Molecular Weight&lt;br /&gt;
| 169.11&lt;br /&gt;
|-&lt;br /&gt;
| Appearance&lt;br /&gt;
| White Crystalline Solid&lt;br /&gt;
|-&lt;br /&gt;
| CAS registry number|CAS number&lt;br /&gt;
|142-47-2&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Properties&lt;br /&gt;
|-&lt;br /&gt;
| Melting point&lt;br /&gt;
| 232 °C (505 K)&lt;br /&gt;
|-&lt;br /&gt;
| Related compounds &lt;br /&gt;
| Glutamic Acid&lt;br /&gt;
|-&lt;br /&gt;
| Solubility in Water&lt;br /&gt;
| 100 mg/100ml&lt;br /&gt;
|-&lt;br /&gt;
| pH&lt;br /&gt;
| 7.0&lt;br /&gt;
|-&lt;br /&gt;
| {{chembox header}} | &amp;lt;small&amp;gt;Except where noted otherwise, data are given for&amp;lt;br /&amp;gt; materials in their [[standard state|standard state (at 25&amp;amp;nbsp;°C, 100&amp;amp;nbsp;kPa)]]&amp;lt;br /&amp;gt;[[wikipedia:Chemical infobox|Infobox disclaimer and references]]&amp;lt;/small&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
|}&lt;br /&gt;
MSG,is a sodium salt of the amino acid &#039;&#039;&#039;&#039;&#039;L-glutamic acid&#039;&#039;&#039;&#039;&#039;. It is practically odorless. It is produced by a bacterial fermentation process with starch or molasses as carbon sources and ammonium salts as nitrogen sources (Steffen process). MSG is not a direct taste enhancer but a complex flavour enhancer for gravies, meats, poultry, sauces, and in other combinations. It is also used to enhance the taste of tobacco and has been used medically to treat hepatic coma.&lt;br /&gt;
&lt;br /&gt;
===3D Representation===&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;green&amp;lt;/color&amp;gt;&lt;br /&gt;
&amp;lt;script&amp;gt;zoom 150; 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;&lt;br /&gt;
HEADER    NONAME 16-Nov-06                                              NONE   1&lt;br /&gt;
TITLE                                                                   NONE   2&lt;br /&gt;
AUTHOR    WWW daemon apache                                             NONE   3&lt;br /&gt;
REVDAT   1  16-Nov-06     0                                             NONE   4&lt;br /&gt;
ATOM      1  O           0       3.779  -0.333   0.251  0.00  0.00           O+0&lt;br /&gt;
ATOM      2  C           0       2.568   0.160  -0.050  0.00  0.00           C+0&lt;br /&gt;
ATOM      3  C           0       1.326  -0.540   0.437  0.00  0.00           C+0&lt;br /&gt;
ATOM      4  C           0       0.089   0.222  -0.042  0.00  0.00           C+0&lt;br /&gt;
ATOM      5  C           0      -1.172  -0.489   0.453  0.00  0.00           C+0&lt;br /&gt;
ATOM      6  H           0      -1.124  -0.603   1.536  0.00  0.00           H+0&lt;br /&gt;
ATOM      7  N           0      -1.265  -1.814  -0.174  0.00  0.00           N+0&lt;br /&gt;
ATOM      8  C           0      -2.385   0.327   0.088  0.00  0.00           C+0&lt;br /&gt;
ATOM      9  O           0      -3.155  -0.075  -0.769  0.00  0.00           O-1&lt;br /&gt;
ATOM     10  O           0      -2.598   1.389   0.648  0.00  0.00           O+0&lt;br /&gt;
ATOM     11  O           0       2.473   1.167  -0.713  0.00  0.00           O+0&lt;br /&gt;
ATOM     12  H           0       4.576   0.116  -0.061  0.00  0.00           H+0&lt;br /&gt;
ATOM     13  H           0       1.302  -1.556   0.041  0.00  0.00           H+0&lt;br /&gt;
ATOM     14  H           0       1.332  -0.575   1.527  0.00  0.00           H+0&lt;br /&gt;
ATOM     15  H           0       0.112   1.238   0.354  0.00  0.00           H+0&lt;br /&gt;
ATOM     16  H           0       0.083   0.257  -1.131  0.00  0.00           H+0&lt;br /&gt;
ATOM     17  H           0      -1.307  -1.660  -1.171  0.00  0.00           H+0&lt;br /&gt;
ATOM     18  H           0      -0.392  -2.284   0.010  0.00  0.00           H+0&lt;br /&gt;
CONECT    1    2   12    0    0                                         NONE  23&lt;br /&gt;
CONECT    2    1    3   11    0                                         NONE  24&lt;br /&gt;
CONECT    3    2    4   13   14                                         NONE  25&lt;br /&gt;
CONECT    4    3    5   15   16                                         NONE  26&lt;br /&gt;
CONECT    5    4    6    7    8                                         NONE  27&lt;br /&gt;
CONECT    7    5   17   18    0                                         NONE  28&lt;br /&gt;
CONECT    8    5    9   10    0                                         NONE  29&lt;br /&gt;
CONECT    9    8    0    0    0                                         NONE  30&lt;br /&gt;
CONECT   10    8    0    0    0                                         NONE  31&lt;br /&gt;
CONECT   11    2    0    0    0                                         NONE  32&lt;br /&gt;
END                                                                     NONE  33&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;
&lt;br /&gt;
&lt;br /&gt;
===Spectra===&lt;br /&gt;
[[Image:NMR of MSG.bmp|600px|&amp;lt;sup&amp;gt;1&amp;lt;/sup&amp;gt;H NMR Spectrum of MSG]]&lt;br /&gt;
&lt;br /&gt;
===Source &amp;amp; Manufacturing===&lt;br /&gt;
Glutamate itself is a naturally occuring amino acid that can be found in human bodies and high-protein foods (eg. nuts, meats and most dairy products). When it is not bound to sodium some of the glutamate is in the &amp;quot;free&amp;quot; ionic form; and only this free form of glutamate can enhance the flavor of foods. Tomatoes also have a high concentration of the free glutamate form making them natural flavour enhancers.&lt;br /&gt;
&lt;br /&gt;
Originally extracted from seaweed, modern MSG is produced by the fermentation of starch, sugar beets, sugar cane, or molasses.&lt;br /&gt;
&lt;br /&gt;
==References &amp;amp; Useful Links==&lt;br /&gt;
Image: http://www.germes-online.com/catalog/48/55/189/257161/monosodium_glutamate.html&lt;br /&gt;
&lt;br /&gt;
http://www.chemicalland21.com/lifescience/foco/MONOSODIUM%20GLUTAMATE.htm&lt;/div&gt;</summary>
		<author><name>Rw305</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It:MSG&amp;diff=5523</id>
		<title>It:MSG</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It:MSG&amp;diff=5523"/>
		<updated>2006-11-20T10:52:40Z</updated>

		<summary type="html">&lt;p&gt;Rw305: /* Source */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;==Abstract==&lt;br /&gt;
[[Image:msg2.bmp|centre|300px|Chemical Structure of MSG]]&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;Monosodium Glutamate&#039;&#039;&#039; is more commonly known as &#039;&#039;&#039;MSG&#039;&#039;&#039; and has become the choice chemical for the enhancement of flavour in many foods. It was originally discovered in 1909 by the Ajinomoto Corporation in Japan.&lt;br /&gt;
&lt;br /&gt;
==The Basics==&lt;br /&gt;
{| class=&amp;quot;toccolours&amp;quot; border=&amp;quot;1&amp;quot; style=&amp;quot;float: right; clear: right; margin: 0 0 1em 1em; border-collapse: collapse;&amp;quot;&lt;br /&gt;
! {{chembox header}} | MSG &lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; width=&amp;quot;300&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image:msg.jpg]]&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | General&lt;br /&gt;
|-&lt;br /&gt;
| IUPAC nomenclature|Systematic name&lt;br /&gt;
|2-aminopentanedioic acid&lt;br /&gt;
|-&lt;br /&gt;
| Other names&lt;br /&gt;
|2-aminoglutaric acid, 1-aminopropane-1,&lt;br /&gt;
3-dicarboxylic acid&lt;br /&gt;
|-&lt;br /&gt;
| Chemical formula|Molecular formula]&lt;br /&gt;
|C&amp;lt;sub&amp;gt;5&amp;lt;/sub&amp;gt;H&amp;lt;sub&amp;gt;8&amp;lt;/sub&amp;gt;NNaO&amp;lt;sub&amp;gt;4&amp;lt;/sub&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
|-&lt;br /&gt;
| Molecular Weight&lt;br /&gt;
| 169.11&lt;br /&gt;
|-&lt;br /&gt;
| Appearance&lt;br /&gt;
| White Crystalline Solid&lt;br /&gt;
|-&lt;br /&gt;
| CAS registry number|CAS number&lt;br /&gt;
|142-47-2&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Properties&lt;br /&gt;
|-&lt;br /&gt;
| Melting point&lt;br /&gt;
| 232 °C (505 K)&lt;br /&gt;
|-&lt;br /&gt;
| Related compounds &lt;br /&gt;
| Glutamic Acid&lt;br /&gt;
|-&lt;br /&gt;
| Solubility in Water&lt;br /&gt;
| 100 mg/100ml&lt;br /&gt;
|-&lt;br /&gt;
| pH&lt;br /&gt;
| 7.0&lt;br /&gt;
|-&lt;br /&gt;
| {{chembox header}} | &amp;lt;small&amp;gt;Except where noted otherwise, data are given for&amp;lt;br /&amp;gt; materials in their [[standard state|standard state (at 25&amp;amp;nbsp;°C, 100&amp;amp;nbsp;kPa)]]&amp;lt;br /&amp;gt;[[wikipedia:Chemical infobox|Infobox disclaimer and references]]&amp;lt;/small&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
|}&lt;br /&gt;
MSG,is a sodium salt of the amino acid &#039;&#039;&#039;&#039;&#039;L-glutamic acid&#039;&#039;&#039;&#039;&#039;. It is practically odorless. It is produced by a bacterial fermentation process with starch or molasses as carbon sources and ammonium salts as nitrogen sources (Steffen process). MSG is not a direct taste enhancer but a complex flavour enhancer for gravies, meats, poultry, sauces, and in other combinations. It is also used to enhance the taste of tobacco and has been used medically to treat hepatic coma.&lt;br /&gt;
&lt;br /&gt;
===3D Representation===&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;green&amp;lt;/color&amp;gt;&lt;br /&gt;
&amp;lt;script&amp;gt;zoom 150; 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;&lt;br /&gt;
HEADER    NONAME 16-Nov-06                                              NONE   1&lt;br /&gt;
TITLE                                                                   NONE   2&lt;br /&gt;
AUTHOR    WWW daemon apache                                             NONE   3&lt;br /&gt;
REVDAT   1  16-Nov-06     0                                             NONE   4&lt;br /&gt;
ATOM      1  O           0       3.779  -0.333   0.251  0.00  0.00           O+0&lt;br /&gt;
ATOM      2  C           0       2.568   0.160  -0.050  0.00  0.00           C+0&lt;br /&gt;
ATOM      3  C           0       1.326  -0.540   0.437  0.00  0.00           C+0&lt;br /&gt;
ATOM      4  C           0       0.089   0.222  -0.042  0.00  0.00           C+0&lt;br /&gt;
ATOM      5  C           0      -1.172  -0.489   0.453  0.00  0.00           C+0&lt;br /&gt;
ATOM      6  H           0      -1.124  -0.603   1.536  0.00  0.00           H+0&lt;br /&gt;
ATOM      7  N           0      -1.265  -1.814  -0.174  0.00  0.00           N+0&lt;br /&gt;
ATOM      8  C           0      -2.385   0.327   0.088  0.00  0.00           C+0&lt;br /&gt;
ATOM      9  O           0      -3.155  -0.075  -0.769  0.00  0.00           O-1&lt;br /&gt;
ATOM     10  O           0      -2.598   1.389   0.648  0.00  0.00           O+0&lt;br /&gt;
ATOM     11  O           0       2.473   1.167  -0.713  0.00  0.00           O+0&lt;br /&gt;
ATOM     12  H           0       4.576   0.116  -0.061  0.00  0.00           H+0&lt;br /&gt;
ATOM     13  H           0       1.302  -1.556   0.041  0.00  0.00           H+0&lt;br /&gt;
ATOM     14  H           0       1.332  -0.575   1.527  0.00  0.00           H+0&lt;br /&gt;
ATOM     15  H           0       0.112   1.238   0.354  0.00  0.00           H+0&lt;br /&gt;
ATOM     16  H           0       0.083   0.257  -1.131  0.00  0.00           H+0&lt;br /&gt;
ATOM     17  H           0      -1.307  -1.660  -1.171  0.00  0.00           H+0&lt;br /&gt;
ATOM     18  H           0      -0.392  -2.284   0.010  0.00  0.00           H+0&lt;br /&gt;
CONECT    1    2   12    0    0                                         NONE  23&lt;br /&gt;
CONECT    2    1    3   11    0                                         NONE  24&lt;br /&gt;
CONECT    3    2    4   13   14                                         NONE  25&lt;br /&gt;
CONECT    4    3    5   15   16                                         NONE  26&lt;br /&gt;
CONECT    5    4    6    7    8                                         NONE  27&lt;br /&gt;
CONECT    7    5   17   18    0                                         NONE  28&lt;br /&gt;
CONECT    8    5    9   10    0                                         NONE  29&lt;br /&gt;
CONECT    9    8    0    0    0                                         NONE  30&lt;br /&gt;
CONECT   10    8    0    0    0                                         NONE  31&lt;br /&gt;
CONECT   11    2    0    0    0                                         NONE  32&lt;br /&gt;
END                                                                     NONE  33&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;
&lt;br /&gt;
&lt;br /&gt;
===Spectra===&lt;br /&gt;
[[Image:NMR of MSG.bmp|600px|&amp;lt;sup&amp;gt;1&amp;lt;/sup&amp;gt;H NMR Spectrum of MSG]]&lt;br /&gt;
&lt;br /&gt;
===Source &amp;amp; Manufacturing===&lt;br /&gt;
Glutamate itself is a naturally occuring amino acid that can be found in human bodies and high-protein foods (eg. nuts, meats and most dairy products). When it is not bound to sodium some of the glutamate is in the &amp;quot;free&amp;quot; ionic form; and only this free form of glutamate can enhance the flavor of foods. Tomatoes also have a high concentration of the free glutamate form making them natural flavour enhancers.&lt;br /&gt;
&lt;br /&gt;
==References &amp;amp; Useful Links==&lt;br /&gt;
Image: http://www.germes-online.com/catalog/48/55/189/257161/monosodium_glutamate.html&lt;br /&gt;
&lt;br /&gt;
http://www.chemicalland21.com/lifescience/foco/MONOSODIUM%20GLUTAMATE.htm&lt;/div&gt;</summary>
		<author><name>Rw305</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It:MSG&amp;diff=5522</id>
		<title>It:MSG</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It:MSG&amp;diff=5522"/>
		<updated>2006-11-20T10:47:02Z</updated>

		<summary type="html">&lt;p&gt;Rw305: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;==Abstract==&lt;br /&gt;
[[Image:msg2.bmp|centre|300px|Chemical Structure of MSG]]&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;Monosodium Glutamate&#039;&#039;&#039; is more commonly known as &#039;&#039;&#039;MSG&#039;&#039;&#039; and has become the choice chemical for the enhancement of flavour in many foods. It was originally discovered in 1909 by the Ajinomoto Corporation in Japan.&lt;br /&gt;
&lt;br /&gt;
==The Basics==&lt;br /&gt;
{| class=&amp;quot;toccolours&amp;quot; border=&amp;quot;1&amp;quot; style=&amp;quot;float: right; clear: right; margin: 0 0 1em 1em; border-collapse: collapse;&amp;quot;&lt;br /&gt;
! {{chembox header}} | MSG &lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; width=&amp;quot;300&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image:msg.jpg]]&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | General&lt;br /&gt;
|-&lt;br /&gt;
| IUPAC nomenclature|Systematic name&lt;br /&gt;
|2-aminopentanedioic acid&lt;br /&gt;
|-&lt;br /&gt;
| Other names&lt;br /&gt;
|2-aminoglutaric acid, 1-aminopropane-1,&lt;br /&gt;
3-dicarboxylic acid&lt;br /&gt;
|-&lt;br /&gt;
| Chemical formula|Molecular formula]&lt;br /&gt;
|C&amp;lt;sub&amp;gt;5&amp;lt;/sub&amp;gt;H&amp;lt;sub&amp;gt;8&amp;lt;/sub&amp;gt;NNaO&amp;lt;sub&amp;gt;4&amp;lt;/sub&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
|-&lt;br /&gt;
| Molecular Weight&lt;br /&gt;
| 169.11&lt;br /&gt;
|-&lt;br /&gt;
| Appearance&lt;br /&gt;
| White Crystalline Solid&lt;br /&gt;
|-&lt;br /&gt;
| CAS registry number|CAS number&lt;br /&gt;
|142-47-2&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Properties&lt;br /&gt;
|-&lt;br /&gt;
| Melting point&lt;br /&gt;
| 232 °C (505 K)&lt;br /&gt;
|-&lt;br /&gt;
| Related compounds &lt;br /&gt;
| Glutamic Acid&lt;br /&gt;
|-&lt;br /&gt;
| Solubility in Water&lt;br /&gt;
| 100 mg/100ml&lt;br /&gt;
|-&lt;br /&gt;
| pH&lt;br /&gt;
| 7.0&lt;br /&gt;
|-&lt;br /&gt;
| {{chembox header}} | &amp;lt;small&amp;gt;Except where noted otherwise, data are given for&amp;lt;br /&amp;gt; materials in their [[standard state|standard state (at 25&amp;amp;nbsp;°C, 100&amp;amp;nbsp;kPa)]]&amp;lt;br /&amp;gt;[[wikipedia:Chemical infobox|Infobox disclaimer and references]]&amp;lt;/small&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
|}&lt;br /&gt;
MSG,is a sodium salt of the amino acid &#039;&#039;&#039;&#039;&#039;L-glutamic acid&#039;&#039;&#039;&#039;&#039;. It is practically odorless. It is produced by a bacterial fermentation process with starch or molasses as carbon sources and ammonium salts as nitrogen sources (Steffen process). MSG is not a direct taste enhancer but a complex flavour enhancer for gravies, meats, poultry, sauces, and in other combinations. It is also used to enhance the taste of tobacco and has been used medically to treat hepatic coma.&lt;br /&gt;
&lt;br /&gt;
===3D Representation===&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;green&amp;lt;/color&amp;gt;&lt;br /&gt;
&amp;lt;script&amp;gt;zoom 150; 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;&lt;br /&gt;
HEADER    NONAME 16-Nov-06                                              NONE   1&lt;br /&gt;
TITLE                                                                   NONE   2&lt;br /&gt;
AUTHOR    WWW daemon apache                                             NONE   3&lt;br /&gt;
REVDAT   1  16-Nov-06     0                                             NONE   4&lt;br /&gt;
ATOM      1  O           0       3.779  -0.333   0.251  0.00  0.00           O+0&lt;br /&gt;
ATOM      2  C           0       2.568   0.160  -0.050  0.00  0.00           C+0&lt;br /&gt;
ATOM      3  C           0       1.326  -0.540   0.437  0.00  0.00           C+0&lt;br /&gt;
ATOM      4  C           0       0.089   0.222  -0.042  0.00  0.00           C+0&lt;br /&gt;
ATOM      5  C           0      -1.172  -0.489   0.453  0.00  0.00           C+0&lt;br /&gt;
ATOM      6  H           0      -1.124  -0.603   1.536  0.00  0.00           H+0&lt;br /&gt;
ATOM      7  N           0      -1.265  -1.814  -0.174  0.00  0.00           N+0&lt;br /&gt;
ATOM      8  C           0      -2.385   0.327   0.088  0.00  0.00           C+0&lt;br /&gt;
ATOM      9  O           0      -3.155  -0.075  -0.769  0.00  0.00           O-1&lt;br /&gt;
ATOM     10  O           0      -2.598   1.389   0.648  0.00  0.00           O+0&lt;br /&gt;
ATOM     11  O           0       2.473   1.167  -0.713  0.00  0.00           O+0&lt;br /&gt;
ATOM     12  H           0       4.576   0.116  -0.061  0.00  0.00           H+0&lt;br /&gt;
ATOM     13  H           0       1.302  -1.556   0.041  0.00  0.00           H+0&lt;br /&gt;
ATOM     14  H           0       1.332  -0.575   1.527  0.00  0.00           H+0&lt;br /&gt;
ATOM     15  H           0       0.112   1.238   0.354  0.00  0.00           H+0&lt;br /&gt;
ATOM     16  H           0       0.083   0.257  -1.131  0.00  0.00           H+0&lt;br /&gt;
ATOM     17  H           0      -1.307  -1.660  -1.171  0.00  0.00           H+0&lt;br /&gt;
ATOM     18  H           0      -0.392  -2.284   0.010  0.00  0.00           H+0&lt;br /&gt;
CONECT    1    2   12    0    0                                         NONE  23&lt;br /&gt;
CONECT    2    1    3   11    0                                         NONE  24&lt;br /&gt;
CONECT    3    2    4   13   14                                         NONE  25&lt;br /&gt;
CONECT    4    3    5   15   16                                         NONE  26&lt;br /&gt;
CONECT    5    4    6    7    8                                         NONE  27&lt;br /&gt;
CONECT    7    5   17   18    0                                         NONE  28&lt;br /&gt;
CONECT    8    5    9   10    0                                         NONE  29&lt;br /&gt;
CONECT    9    8    0    0    0                                         NONE  30&lt;br /&gt;
CONECT   10    8    0    0    0                                         NONE  31&lt;br /&gt;
CONECT   11    2    0    0    0                                         NONE  32&lt;br /&gt;
END                                                                     NONE  33&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;
&lt;br /&gt;
&lt;br /&gt;
===Spectra===&lt;br /&gt;
[[Image:NMR of MSG.bmp|600px|&amp;lt;sup&amp;gt;1&amp;lt;/sup&amp;gt;H NMR Spectrum of MSG]]&lt;br /&gt;
&lt;br /&gt;
===Source===&lt;br /&gt;
&lt;br /&gt;
==References &amp;amp; Useful Links==&lt;br /&gt;
Image: http://www.germes-online.com/catalog/48/55/189/257161/monosodium_glutamate.html&lt;br /&gt;
&lt;br /&gt;
http://www.chemicalland21.com/lifescience/foco/MONOSODIUM%20GLUTAMATE.htm&lt;/div&gt;</summary>
		<author><name>Rw305</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It:MSG&amp;diff=5521</id>
		<title>It:MSG</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It:MSG&amp;diff=5521"/>
		<updated>2006-11-20T10:40:00Z</updated>

		<summary type="html">&lt;p&gt;Rw305: /* Spectra */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;==Abstract==&lt;br /&gt;
[[Image:msg2.bmp|centre|300px|Chemical Structure of MSG]]&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;Monosodium Glutamate&#039;&#039;&#039; is more commonly known as &#039;&#039;&#039;MSG&#039;&#039;&#039; and has become the choice chemical for the enhancement of flavour in many foods. It was originally discovered in 1909 by the Ajinomoto Corporation in Japan.&lt;br /&gt;
&lt;br /&gt;
==The Basics==&lt;br /&gt;
{| class=&amp;quot;toccolours&amp;quot; border=&amp;quot;1&amp;quot; style=&amp;quot;float: right; clear: right; margin: 0 0 1em 1em; border-collapse: collapse;&amp;quot;&lt;br /&gt;
! {{chembox header}} | MSG &lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; width=&amp;quot;300&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image:msg.jpg]]&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | General&lt;br /&gt;
|-&lt;br /&gt;
| IUPAC nomenclature|Systematic name&lt;br /&gt;
|2-aminopentanedioic acid&lt;br /&gt;
|-&lt;br /&gt;
| Other names&lt;br /&gt;
|2-aminoglutaric acid, 1-aminopropane-1,&lt;br /&gt;
3-dicarboxylic acid&lt;br /&gt;
|-&lt;br /&gt;
| Chemical formula|Molecular formula]&lt;br /&gt;
|C&amp;lt;sub&amp;gt;5&amp;lt;/sub&amp;gt;H&amp;lt;sub&amp;gt;8&amp;lt;/sub&amp;gt;NNaO&amp;lt;sub&amp;gt;4&amp;lt;/sub&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
|-&lt;br /&gt;
| Molecular Weight&lt;br /&gt;
| 169.11&lt;br /&gt;
|-&lt;br /&gt;
| Appearance&lt;br /&gt;
| White Crystalline Solid&lt;br /&gt;
|-&lt;br /&gt;
| CAS registry number|CAS number&lt;br /&gt;
|142-47-2&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Properties&lt;br /&gt;
|-&lt;br /&gt;
| Melting point&lt;br /&gt;
| 232 °C (505 K)&lt;br /&gt;
|-&lt;br /&gt;
| Related compounds &lt;br /&gt;
| Glutamic Acid&lt;br /&gt;
|-&lt;br /&gt;
| Solubility in Water&lt;br /&gt;
| 100 mg/100ml&lt;br /&gt;
|-&lt;br /&gt;
| pH&lt;br /&gt;
| 7.0&lt;br /&gt;
|-&lt;br /&gt;
| {{chembox header}} | &amp;lt;small&amp;gt;Except where noted otherwise, data are given for&amp;lt;br /&amp;gt; materials in their [[standard state|standard state (at 25&amp;amp;nbsp;°C, 100&amp;amp;nbsp;kPa)]]&amp;lt;br /&amp;gt;[[wikipedia:Chemical infobox|Infobox disclaimer and references]]&amp;lt;/small&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
|}&lt;br /&gt;
MSG,is a sodium salt of the amino acid &#039;&#039;&#039;&#039;&#039;L-glutamic acid&#039;&#039;&#039;&#039;&#039;. It is practically odorless. It is produced by a bacterial fermentation process with starch or molasses as carbon sources and ammonium salts as nitrogen sources (Steffen process). MSG is not a direct taste enhancer but a complex flavour enhancer for gravies, meats, poultry, sauces, and in other combinations. It is also used to enhance the taste of tobacco and has been used medically to treat hepatic coma.&lt;br /&gt;
&lt;br /&gt;
===3D Representation===&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;green&amp;lt;/color&amp;gt;&lt;br /&gt;
&amp;lt;script&amp;gt;zoom 150; 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;&lt;br /&gt;
HEADER    NONAME 16-Nov-06                                              NONE   1&lt;br /&gt;
TITLE                                                                   NONE   2&lt;br /&gt;
AUTHOR    WWW daemon apache                                             NONE   3&lt;br /&gt;
REVDAT   1  16-Nov-06     0                                             NONE   4&lt;br /&gt;
ATOM      1  O           0       3.779  -0.333   0.251  0.00  0.00           O+0&lt;br /&gt;
ATOM      2  C           0       2.568   0.160  -0.050  0.00  0.00           C+0&lt;br /&gt;
ATOM      3  C           0       1.326  -0.540   0.437  0.00  0.00           C+0&lt;br /&gt;
ATOM      4  C           0       0.089   0.222  -0.042  0.00  0.00           C+0&lt;br /&gt;
ATOM      5  C           0      -1.172  -0.489   0.453  0.00  0.00           C+0&lt;br /&gt;
ATOM      6  H           0      -1.124  -0.603   1.536  0.00  0.00           H+0&lt;br /&gt;
ATOM      7  N           0      -1.265  -1.814  -0.174  0.00  0.00           N+0&lt;br /&gt;
ATOM      8  C           0      -2.385   0.327   0.088  0.00  0.00           C+0&lt;br /&gt;
ATOM      9  O           0      -3.155  -0.075  -0.769  0.00  0.00           O-1&lt;br /&gt;
ATOM     10  O           0      -2.598   1.389   0.648  0.00  0.00           O+0&lt;br /&gt;
ATOM     11  O           0       2.473   1.167  -0.713  0.00  0.00           O+0&lt;br /&gt;
ATOM     12  H           0       4.576   0.116  -0.061  0.00  0.00           H+0&lt;br /&gt;
ATOM     13  H           0       1.302  -1.556   0.041  0.00  0.00           H+0&lt;br /&gt;
ATOM     14  H           0       1.332  -0.575   1.527  0.00  0.00           H+0&lt;br /&gt;
ATOM     15  H           0       0.112   1.238   0.354  0.00  0.00           H+0&lt;br /&gt;
ATOM     16  H           0       0.083   0.257  -1.131  0.00  0.00           H+0&lt;br /&gt;
ATOM     17  H           0      -1.307  -1.660  -1.171  0.00  0.00           H+0&lt;br /&gt;
ATOM     18  H           0      -0.392  -2.284   0.010  0.00  0.00           H+0&lt;br /&gt;
CONECT    1    2   12    0    0                                         NONE  23&lt;br /&gt;
CONECT    2    1    3   11    0                                         NONE  24&lt;br /&gt;
CONECT    3    2    4   13   14                                         NONE  25&lt;br /&gt;
CONECT    4    3    5   15   16                                         NONE  26&lt;br /&gt;
CONECT    5    4    6    7    8                                         NONE  27&lt;br /&gt;
CONECT    7    5   17   18    0                                         NONE  28&lt;br /&gt;
CONECT    8    5    9   10    0                                         NONE  29&lt;br /&gt;
CONECT    9    8    0    0    0                                         NONE  30&lt;br /&gt;
CONECT   10    8    0    0    0                                         NONE  31&lt;br /&gt;
CONECT   11    2    0    0    0                                         NONE  32&lt;br /&gt;
END                                                                     NONE  33&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;
&lt;br /&gt;
&lt;br /&gt;
===Spectra===&lt;br /&gt;
[[Image:NMR of MSG.bmp|600px|&amp;lt;sup&amp;gt;1&amp;lt;/sup&amp;gt;H NMR Spectrum of MSG]]&lt;br /&gt;
&lt;br /&gt;
==References &amp;amp; Useful Links==&lt;br /&gt;
Image: http://www.germes-online.com/catalog/48/55/189/257161/monosodium_glutamate.html&lt;br /&gt;
&lt;br /&gt;
http://www.chemicalland21.com/lifescience/foco/MONOSODIUM%20GLUTAMATE.htm&lt;/div&gt;</summary>
		<author><name>Rw305</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It:MSG&amp;diff=5520</id>
		<title>It:MSG</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It:MSG&amp;diff=5520"/>
		<updated>2006-11-20T10:39:44Z</updated>

		<summary type="html">&lt;p&gt;Rw305: /* Spectra */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;==Abstract==&lt;br /&gt;
[[Image:msg2.bmp|centre|300px|Chemical Structure of MSG]]&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;Monosodium Glutamate&#039;&#039;&#039; is more commonly known as &#039;&#039;&#039;MSG&#039;&#039;&#039; and has become the choice chemical for the enhancement of flavour in many foods. It was originally discovered in 1909 by the Ajinomoto Corporation in Japan.&lt;br /&gt;
&lt;br /&gt;
==The Basics==&lt;br /&gt;
{| class=&amp;quot;toccolours&amp;quot; border=&amp;quot;1&amp;quot; style=&amp;quot;float: right; clear: right; margin: 0 0 1em 1em; border-collapse: collapse;&amp;quot;&lt;br /&gt;
! {{chembox header}} | MSG &lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; width=&amp;quot;300&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image:msg.jpg]]&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | General&lt;br /&gt;
|-&lt;br /&gt;
| IUPAC nomenclature|Systematic name&lt;br /&gt;
|2-aminopentanedioic acid&lt;br /&gt;
|-&lt;br /&gt;
| Other names&lt;br /&gt;
|2-aminoglutaric acid, 1-aminopropane-1,&lt;br /&gt;
3-dicarboxylic acid&lt;br /&gt;
|-&lt;br /&gt;
| Chemical formula|Molecular formula]&lt;br /&gt;
|C&amp;lt;sub&amp;gt;5&amp;lt;/sub&amp;gt;H&amp;lt;sub&amp;gt;8&amp;lt;/sub&amp;gt;NNaO&amp;lt;sub&amp;gt;4&amp;lt;/sub&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
|-&lt;br /&gt;
| Molecular Weight&lt;br /&gt;
| 169.11&lt;br /&gt;
|-&lt;br /&gt;
| Appearance&lt;br /&gt;
| White Crystalline Solid&lt;br /&gt;
|-&lt;br /&gt;
| CAS registry number|CAS number&lt;br /&gt;
|142-47-2&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Properties&lt;br /&gt;
|-&lt;br /&gt;
| Melting point&lt;br /&gt;
| 232 °C (505 K)&lt;br /&gt;
|-&lt;br /&gt;
| Related compounds &lt;br /&gt;
| Glutamic Acid&lt;br /&gt;
|-&lt;br /&gt;
| Solubility in Water&lt;br /&gt;
| 100 mg/100ml&lt;br /&gt;
|-&lt;br /&gt;
| pH&lt;br /&gt;
| 7.0&lt;br /&gt;
|-&lt;br /&gt;
| {{chembox header}} | &amp;lt;small&amp;gt;Except where noted otherwise, data are given for&amp;lt;br /&amp;gt; materials in their [[standard state|standard state (at 25&amp;amp;nbsp;°C, 100&amp;amp;nbsp;kPa)]]&amp;lt;br /&amp;gt;[[wikipedia:Chemical infobox|Infobox disclaimer and references]]&amp;lt;/small&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
|}&lt;br /&gt;
MSG,is a sodium salt of the amino acid &#039;&#039;&#039;&#039;&#039;L-glutamic acid&#039;&#039;&#039;&#039;&#039;. It is practically odorless. It is produced by a bacterial fermentation process with starch or molasses as carbon sources and ammonium salts as nitrogen sources (Steffen process). MSG is not a direct taste enhancer but a complex flavour enhancer for gravies, meats, poultry, sauces, and in other combinations. It is also used to enhance the taste of tobacco and has been used medically to treat hepatic coma.&lt;br /&gt;
&lt;br /&gt;
===3D Representation===&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;green&amp;lt;/color&amp;gt;&lt;br /&gt;
&amp;lt;script&amp;gt;zoom 150; 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;&lt;br /&gt;
HEADER    NONAME 16-Nov-06                                              NONE   1&lt;br /&gt;
TITLE                                                                   NONE   2&lt;br /&gt;
AUTHOR    WWW daemon apache                                             NONE   3&lt;br /&gt;
REVDAT   1  16-Nov-06     0                                             NONE   4&lt;br /&gt;
ATOM      1  O           0       3.779  -0.333   0.251  0.00  0.00           O+0&lt;br /&gt;
ATOM      2  C           0       2.568   0.160  -0.050  0.00  0.00           C+0&lt;br /&gt;
ATOM      3  C           0       1.326  -0.540   0.437  0.00  0.00           C+0&lt;br /&gt;
ATOM      4  C           0       0.089   0.222  -0.042  0.00  0.00           C+0&lt;br /&gt;
ATOM      5  C           0      -1.172  -0.489   0.453  0.00  0.00           C+0&lt;br /&gt;
ATOM      6  H           0      -1.124  -0.603   1.536  0.00  0.00           H+0&lt;br /&gt;
ATOM      7  N           0      -1.265  -1.814  -0.174  0.00  0.00           N+0&lt;br /&gt;
ATOM      8  C           0      -2.385   0.327   0.088  0.00  0.00           C+0&lt;br /&gt;
ATOM      9  O           0      -3.155  -0.075  -0.769  0.00  0.00           O-1&lt;br /&gt;
ATOM     10  O           0      -2.598   1.389   0.648  0.00  0.00           O+0&lt;br /&gt;
ATOM     11  O           0       2.473   1.167  -0.713  0.00  0.00           O+0&lt;br /&gt;
ATOM     12  H           0       4.576   0.116  -0.061  0.00  0.00           H+0&lt;br /&gt;
ATOM     13  H           0       1.302  -1.556   0.041  0.00  0.00           H+0&lt;br /&gt;
ATOM     14  H           0       1.332  -0.575   1.527  0.00  0.00           H+0&lt;br /&gt;
ATOM     15  H           0       0.112   1.238   0.354  0.00  0.00           H+0&lt;br /&gt;
ATOM     16  H           0       0.083   0.257  -1.131  0.00  0.00           H+0&lt;br /&gt;
ATOM     17  H           0      -1.307  -1.660  -1.171  0.00  0.00           H+0&lt;br /&gt;
ATOM     18  H           0      -0.392  -2.284   0.010  0.00  0.00           H+0&lt;br /&gt;
CONECT    1    2   12    0    0                                         NONE  23&lt;br /&gt;
CONECT    2    1    3   11    0                                         NONE  24&lt;br /&gt;
CONECT    3    2    4   13   14                                         NONE  25&lt;br /&gt;
CONECT    4    3    5   15   16                                         NONE  26&lt;br /&gt;
CONECT    5    4    6    7    8                                         NONE  27&lt;br /&gt;
CONECT    7    5   17   18    0                                         NONE  28&lt;br /&gt;
CONECT    8    5    9   10    0                                         NONE  29&lt;br /&gt;
CONECT    9    8    0    0    0                                         NONE  30&lt;br /&gt;
CONECT   10    8    0    0    0                                         NONE  31&lt;br /&gt;
CONECT   11    2    0    0    0                                         NONE  32&lt;br /&gt;
END                                                                     NONE  33&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;
&lt;br /&gt;
&lt;br /&gt;
===Spectra===&lt;br /&gt;
[[Image:NMR of MSG.bmp|600px]|&amp;lt;sup&amp;gt;1&amp;lt;/sup&amp;gt;H NMR Spectrum of MSG]&lt;br /&gt;
&lt;br /&gt;
==References &amp;amp; Useful Links==&lt;br /&gt;
Image: http://www.germes-online.com/catalog/48/55/189/257161/monosodium_glutamate.html&lt;br /&gt;
&lt;br /&gt;
http://www.chemicalland21.com/lifescience/foco/MONOSODIUM%20GLUTAMATE.htm&lt;/div&gt;</summary>
		<author><name>Rw305</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It:MSG&amp;diff=5477</id>
		<title>It:MSG</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It:MSG&amp;diff=5477"/>
		<updated>2006-11-16T14:42:31Z</updated>

		<summary type="html">&lt;p&gt;Rw305: /* Spectra */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;==Abstract==&lt;br /&gt;
[[Image:msg2.bmp|centre|300px|Chemical Structure of MSG]]&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;Monosodium Glutamate&#039;&#039;&#039; is more commonly known as &#039;&#039;&#039;MSG&#039;&#039;&#039; and has become the choice chemical for the enhancement of flavour in many foods. It was originally discovered in 1909 by the Ajinomoto Corporation in Japan.&lt;br /&gt;
&lt;br /&gt;
==The Basics==&lt;br /&gt;
{| class=&amp;quot;toccolours&amp;quot; border=&amp;quot;1&amp;quot; style=&amp;quot;float: right; clear: right; margin: 0 0 1em 1em; border-collapse: collapse;&amp;quot;&lt;br /&gt;
! {{chembox header}} | MSG &lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; width=&amp;quot;300&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image:msg.jpg]]&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | General&lt;br /&gt;
|-&lt;br /&gt;
| IUPAC nomenclature|Systematic name&lt;br /&gt;
|2-aminopentanedioic acid&lt;br /&gt;
|-&lt;br /&gt;
| Other names&lt;br /&gt;
|2-aminoglutaric acid, 1-aminopropane-1,&lt;br /&gt;
3-dicarboxylic acid&lt;br /&gt;
|-&lt;br /&gt;
| Chemical formula|Molecular formula]&lt;br /&gt;
|C&amp;lt;sub&amp;gt;5&amp;lt;/sub&amp;gt;H&amp;lt;sub&amp;gt;8&amp;lt;/sub&amp;gt;NNaO&amp;lt;sub&amp;gt;4&amp;lt;/sub&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
|-&lt;br /&gt;
| Molecular Weight&lt;br /&gt;
| 169.11&lt;br /&gt;
|-&lt;br /&gt;
| Appearance&lt;br /&gt;
| White Crystalline Solid&lt;br /&gt;
|-&lt;br /&gt;
| CAS registry number|CAS number&lt;br /&gt;
|142-47-2&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Properties&lt;br /&gt;
|-&lt;br /&gt;
| Melting point&lt;br /&gt;
| 232 °C (505 K)&lt;br /&gt;
|-&lt;br /&gt;
| Related compounds &lt;br /&gt;
| Glutamic Acid&lt;br /&gt;
|-&lt;br /&gt;
| Solubility in Water&lt;br /&gt;
| 100 mg/100ml&lt;br /&gt;
|-&lt;br /&gt;
| pH&lt;br /&gt;
| 7.0&lt;br /&gt;
|-&lt;br /&gt;
| {{chembox header}} | &amp;lt;small&amp;gt;Except where noted otherwise, data are given for&amp;lt;br /&amp;gt; materials in their [[standard state|standard state (at 25&amp;amp;nbsp;°C, 100&amp;amp;nbsp;kPa)]]&amp;lt;br /&amp;gt;[[wikipedia:Chemical infobox|Infobox disclaimer and references]]&amp;lt;/small&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
|}&lt;br /&gt;
MSG,is a sodium salt of the amino acid &#039;&#039;&#039;&#039;&#039;L-glutamic acid&#039;&#039;&#039;&#039;&#039;. It is practically odorless. It is produced by a bacterial fermentation process with starch or molasses as carbon sources and ammonium salts as nitrogen sources (Steffen process). MSG is not a direct taste enhancer but a complex flavour enhancer for gravies, meats, poultry, sauces, and in other combinations. It is also used to enhance the taste of tobacco and has been used medically to treat hepatic coma.&lt;br /&gt;
&lt;br /&gt;
===3D Representation===&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;green&amp;lt;/color&amp;gt;&lt;br /&gt;
&amp;lt;script&amp;gt;zoom 150; 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;&lt;br /&gt;
HEADER    NONAME 16-Nov-06                                              NONE   1&lt;br /&gt;
TITLE                                                                   NONE   2&lt;br /&gt;
AUTHOR    WWW daemon apache                                             NONE   3&lt;br /&gt;
REVDAT   1  16-Nov-06     0                                             NONE   4&lt;br /&gt;
ATOM      1  O           0       3.779  -0.333   0.251  0.00  0.00           O+0&lt;br /&gt;
ATOM      2  C           0       2.568   0.160  -0.050  0.00  0.00           C+0&lt;br /&gt;
ATOM      3  C           0       1.326  -0.540   0.437  0.00  0.00           C+0&lt;br /&gt;
ATOM      4  C           0       0.089   0.222  -0.042  0.00  0.00           C+0&lt;br /&gt;
ATOM      5  C           0      -1.172  -0.489   0.453  0.00  0.00           C+0&lt;br /&gt;
ATOM      6  H           0      -1.124  -0.603   1.536  0.00  0.00           H+0&lt;br /&gt;
ATOM      7  N           0      -1.265  -1.814  -0.174  0.00  0.00           N+0&lt;br /&gt;
ATOM      8  C           0      -2.385   0.327   0.088  0.00  0.00           C+0&lt;br /&gt;
ATOM      9  O           0      -3.155  -0.075  -0.769  0.00  0.00           O-1&lt;br /&gt;
ATOM     10  O           0      -2.598   1.389   0.648  0.00  0.00           O+0&lt;br /&gt;
ATOM     11  O           0       2.473   1.167  -0.713  0.00  0.00           O+0&lt;br /&gt;
ATOM     12  H           0       4.576   0.116  -0.061  0.00  0.00           H+0&lt;br /&gt;
ATOM     13  H           0       1.302  -1.556   0.041  0.00  0.00           H+0&lt;br /&gt;
ATOM     14  H           0       1.332  -0.575   1.527  0.00  0.00           H+0&lt;br /&gt;
ATOM     15  H           0       0.112   1.238   0.354  0.00  0.00           H+0&lt;br /&gt;
ATOM     16  H           0       0.083   0.257  -1.131  0.00  0.00           H+0&lt;br /&gt;
ATOM     17  H           0      -1.307  -1.660  -1.171  0.00  0.00           H+0&lt;br /&gt;
ATOM     18  H           0      -0.392  -2.284   0.010  0.00  0.00           H+0&lt;br /&gt;
CONECT    1    2   12    0    0                                         NONE  23&lt;br /&gt;
CONECT    2    1    3   11    0                                         NONE  24&lt;br /&gt;
CONECT    3    2    4   13   14                                         NONE  25&lt;br /&gt;
CONECT    4    3    5   15   16                                         NONE  26&lt;br /&gt;
CONECT    5    4    6    7    8                                         NONE  27&lt;br /&gt;
CONECT    7    5   17   18    0                                         NONE  28&lt;br /&gt;
CONECT    8    5    9   10    0                                         NONE  29&lt;br /&gt;
CONECT    9    8    0    0    0                                         NONE  30&lt;br /&gt;
CONECT   10    8    0    0    0                                         NONE  31&lt;br /&gt;
CONECT   11    2    0    0    0                                         NONE  32&lt;br /&gt;
END                                                                     NONE  33&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;
&lt;br /&gt;
&lt;br /&gt;
===Spectra===&lt;br /&gt;
[[Image:NMR of MSG.bmp|600px]]&lt;br /&gt;
&lt;br /&gt;
==References &amp;amp; Useful Links==&lt;br /&gt;
Image: http://www.germes-online.com/catalog/48/55/189/257161/monosodium_glutamate.html&lt;br /&gt;
&lt;br /&gt;
http://www.chemicalland21.com/lifescience/foco/MONOSODIUM%20GLUTAMATE.htm&lt;/div&gt;</summary>
		<author><name>Rw305</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It:MSG&amp;diff=5476</id>
		<title>It:MSG</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It:MSG&amp;diff=5476"/>
		<updated>2006-11-16T14:42:06Z</updated>

		<summary type="html">&lt;p&gt;Rw305: /* Spectra */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;==Abstract==&lt;br /&gt;
[[Image:msg2.bmp|centre|300px|Chemical Structure of MSG]]&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;Monosodium Glutamate&#039;&#039;&#039; is more commonly known as &#039;&#039;&#039;MSG&#039;&#039;&#039; and has become the choice chemical for the enhancement of flavour in many foods. It was originally discovered in 1909 by the Ajinomoto Corporation in Japan.&lt;br /&gt;
&lt;br /&gt;
==The Basics==&lt;br /&gt;
{| class=&amp;quot;toccolours&amp;quot; border=&amp;quot;1&amp;quot; style=&amp;quot;float: right; clear: right; margin: 0 0 1em 1em; border-collapse: collapse;&amp;quot;&lt;br /&gt;
! {{chembox header}} | MSG &lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; width=&amp;quot;300&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image:msg.jpg]]&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | General&lt;br /&gt;
|-&lt;br /&gt;
| IUPAC nomenclature|Systematic name&lt;br /&gt;
|2-aminopentanedioic acid&lt;br /&gt;
|-&lt;br /&gt;
| Other names&lt;br /&gt;
|2-aminoglutaric acid, 1-aminopropane-1,&lt;br /&gt;
3-dicarboxylic acid&lt;br /&gt;
|-&lt;br /&gt;
| Chemical formula|Molecular formula]&lt;br /&gt;
|C&amp;lt;sub&amp;gt;5&amp;lt;/sub&amp;gt;H&amp;lt;sub&amp;gt;8&amp;lt;/sub&amp;gt;NNaO&amp;lt;sub&amp;gt;4&amp;lt;/sub&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
|-&lt;br /&gt;
| Molecular Weight&lt;br /&gt;
| 169.11&lt;br /&gt;
|-&lt;br /&gt;
| Appearance&lt;br /&gt;
| White Crystalline Solid&lt;br /&gt;
|-&lt;br /&gt;
| CAS registry number|CAS number&lt;br /&gt;
|142-47-2&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Properties&lt;br /&gt;
|-&lt;br /&gt;
| Melting point&lt;br /&gt;
| 232 °C (505 K)&lt;br /&gt;
|-&lt;br /&gt;
| Related compounds &lt;br /&gt;
| Glutamic Acid&lt;br /&gt;
|-&lt;br /&gt;
| Solubility in Water&lt;br /&gt;
| 100 mg/100ml&lt;br /&gt;
|-&lt;br /&gt;
| pH&lt;br /&gt;
| 7.0&lt;br /&gt;
|-&lt;br /&gt;
| {{chembox header}} | &amp;lt;small&amp;gt;Except where noted otherwise, data are given for&amp;lt;br /&amp;gt; materials in their [[standard state|standard state (at 25&amp;amp;nbsp;°C, 100&amp;amp;nbsp;kPa)]]&amp;lt;br /&amp;gt;[[wikipedia:Chemical infobox|Infobox disclaimer and references]]&amp;lt;/small&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
|}&lt;br /&gt;
MSG,is a sodium salt of the amino acid &#039;&#039;&#039;&#039;&#039;L-glutamic acid&#039;&#039;&#039;&#039;&#039;. It is practically odorless. It is produced by a bacterial fermentation process with starch or molasses as carbon sources and ammonium salts as nitrogen sources (Steffen process). MSG is not a direct taste enhancer but a complex flavour enhancer for gravies, meats, poultry, sauces, and in other combinations. It is also used to enhance the taste of tobacco and has been used medically to treat hepatic coma.&lt;br /&gt;
&lt;br /&gt;
===3D Representation===&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;green&amp;lt;/color&amp;gt;&lt;br /&gt;
&amp;lt;script&amp;gt;zoom 150; 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;&lt;br /&gt;
HEADER    NONAME 16-Nov-06                                              NONE   1&lt;br /&gt;
TITLE                                                                   NONE   2&lt;br /&gt;
AUTHOR    WWW daemon apache                                             NONE   3&lt;br /&gt;
REVDAT   1  16-Nov-06     0                                             NONE   4&lt;br /&gt;
ATOM      1  O           0       3.779  -0.333   0.251  0.00  0.00           O+0&lt;br /&gt;
ATOM      2  C           0       2.568   0.160  -0.050  0.00  0.00           C+0&lt;br /&gt;
ATOM      3  C           0       1.326  -0.540   0.437  0.00  0.00           C+0&lt;br /&gt;
ATOM      4  C           0       0.089   0.222  -0.042  0.00  0.00           C+0&lt;br /&gt;
ATOM      5  C           0      -1.172  -0.489   0.453  0.00  0.00           C+0&lt;br /&gt;
ATOM      6  H           0      -1.124  -0.603   1.536  0.00  0.00           H+0&lt;br /&gt;
ATOM      7  N           0      -1.265  -1.814  -0.174  0.00  0.00           N+0&lt;br /&gt;
ATOM      8  C           0      -2.385   0.327   0.088  0.00  0.00           C+0&lt;br /&gt;
ATOM      9  O           0      -3.155  -0.075  -0.769  0.00  0.00           O-1&lt;br /&gt;
ATOM     10  O           0      -2.598   1.389   0.648  0.00  0.00           O+0&lt;br /&gt;
ATOM     11  O           0       2.473   1.167  -0.713  0.00  0.00           O+0&lt;br /&gt;
ATOM     12  H           0       4.576   0.116  -0.061  0.00  0.00           H+0&lt;br /&gt;
ATOM     13  H           0       1.302  -1.556   0.041  0.00  0.00           H+0&lt;br /&gt;
ATOM     14  H           0       1.332  -0.575   1.527  0.00  0.00           H+0&lt;br /&gt;
ATOM     15  H           0       0.112   1.238   0.354  0.00  0.00           H+0&lt;br /&gt;
ATOM     16  H           0       0.083   0.257  -1.131  0.00  0.00           H+0&lt;br /&gt;
ATOM     17  H           0      -1.307  -1.660  -1.171  0.00  0.00           H+0&lt;br /&gt;
ATOM     18  H           0      -0.392  -2.284   0.010  0.00  0.00           H+0&lt;br /&gt;
CONECT    1    2   12    0    0                                         NONE  23&lt;br /&gt;
CONECT    2    1    3   11    0                                         NONE  24&lt;br /&gt;
CONECT    3    2    4   13   14                                         NONE  25&lt;br /&gt;
CONECT    4    3    5   15   16                                         NONE  26&lt;br /&gt;
CONECT    5    4    6    7    8                                         NONE  27&lt;br /&gt;
CONECT    7    5   17   18    0                                         NONE  28&lt;br /&gt;
CONECT    8    5    9   10    0                                         NONE  29&lt;br /&gt;
CONECT    9    8    0    0    0                                         NONE  30&lt;br /&gt;
CONECT   10    8    0    0    0                                         NONE  31&lt;br /&gt;
CONECT   11    2    0    0    0                                         NONE  32&lt;br /&gt;
END                                                                     NONE  33&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;
&lt;br /&gt;
&lt;br /&gt;
===Spectra===&lt;br /&gt;
[[Image:NMR of MSG.bmp]|600px]&lt;br /&gt;
&lt;br /&gt;
==References &amp;amp; Useful Links==&lt;br /&gt;
Image: http://www.germes-online.com/catalog/48/55/189/257161/monosodium_glutamate.html&lt;br /&gt;
&lt;br /&gt;
http://www.chemicalland21.com/lifescience/foco/MONOSODIUM%20GLUTAMATE.htm&lt;/div&gt;</summary>
		<author><name>Rw305</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=File:NMR_of_MSG.bmp&amp;diff=5475</id>
		<title>File:NMR of MSG.bmp</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=File:NMR_of_MSG.bmp&amp;diff=5475"/>
		<updated>2006-11-16T14:41:23Z</updated>

		<summary type="html">&lt;p&gt;Rw305: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;/div&gt;</summary>
		<author><name>Rw305</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It:MSG&amp;diff=5474</id>
		<title>It:MSG</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It:MSG&amp;diff=5474"/>
		<updated>2006-11-16T14:41:11Z</updated>

		<summary type="html">&lt;p&gt;Rw305: /* Spectra */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;==Abstract==&lt;br /&gt;
[[Image:msg2.bmp|centre|300px|Chemical Structure of MSG]]&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;Monosodium Glutamate&#039;&#039;&#039; is more commonly known as &#039;&#039;&#039;MSG&#039;&#039;&#039; and has become the choice chemical for the enhancement of flavour in many foods. It was originally discovered in 1909 by the Ajinomoto Corporation in Japan.&lt;br /&gt;
&lt;br /&gt;
==The Basics==&lt;br /&gt;
{| class=&amp;quot;toccolours&amp;quot; border=&amp;quot;1&amp;quot; style=&amp;quot;float: right; clear: right; margin: 0 0 1em 1em; border-collapse: collapse;&amp;quot;&lt;br /&gt;
! {{chembox header}} | MSG &lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; width=&amp;quot;300&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image:msg.jpg]]&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | General&lt;br /&gt;
|-&lt;br /&gt;
| IUPAC nomenclature|Systematic name&lt;br /&gt;
|2-aminopentanedioic acid&lt;br /&gt;
|-&lt;br /&gt;
| Other names&lt;br /&gt;
|2-aminoglutaric acid, 1-aminopropane-1,&lt;br /&gt;
3-dicarboxylic acid&lt;br /&gt;
|-&lt;br /&gt;
| Chemical formula|Molecular formula]&lt;br /&gt;
|C&amp;lt;sub&amp;gt;5&amp;lt;/sub&amp;gt;H&amp;lt;sub&amp;gt;8&amp;lt;/sub&amp;gt;NNaO&amp;lt;sub&amp;gt;4&amp;lt;/sub&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
|-&lt;br /&gt;
| Molecular Weight&lt;br /&gt;
| 169.11&lt;br /&gt;
|-&lt;br /&gt;
| Appearance&lt;br /&gt;
| White Crystalline Solid&lt;br /&gt;
|-&lt;br /&gt;
| CAS registry number|CAS number&lt;br /&gt;
|142-47-2&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Properties&lt;br /&gt;
|-&lt;br /&gt;
| Melting point&lt;br /&gt;
| 232 °C (505 K)&lt;br /&gt;
|-&lt;br /&gt;
| Related compounds &lt;br /&gt;
| Glutamic Acid&lt;br /&gt;
|-&lt;br /&gt;
| Solubility in Water&lt;br /&gt;
| 100 mg/100ml&lt;br /&gt;
|-&lt;br /&gt;
| pH&lt;br /&gt;
| 7.0&lt;br /&gt;
|-&lt;br /&gt;
| {{chembox header}} | &amp;lt;small&amp;gt;Except where noted otherwise, data are given for&amp;lt;br /&amp;gt; materials in their [[standard state|standard state (at 25&amp;amp;nbsp;°C, 100&amp;amp;nbsp;kPa)]]&amp;lt;br /&amp;gt;[[wikipedia:Chemical infobox|Infobox disclaimer and references]]&amp;lt;/small&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
|}&lt;br /&gt;
MSG,is a sodium salt of the amino acid &#039;&#039;&#039;&#039;&#039;L-glutamic acid&#039;&#039;&#039;&#039;&#039;. It is practically odorless. It is produced by a bacterial fermentation process with starch or molasses as carbon sources and ammonium salts as nitrogen sources (Steffen process). MSG is not a direct taste enhancer but a complex flavour enhancer for gravies, meats, poultry, sauces, and in other combinations. It is also used to enhance the taste of tobacco and has been used medically to treat hepatic coma.&lt;br /&gt;
&lt;br /&gt;
===3D Representation===&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;green&amp;lt;/color&amp;gt;&lt;br /&gt;
&amp;lt;script&amp;gt;zoom 150; 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;&lt;br /&gt;
HEADER    NONAME 16-Nov-06                                              NONE   1&lt;br /&gt;
TITLE                                                                   NONE   2&lt;br /&gt;
AUTHOR    WWW daemon apache                                             NONE   3&lt;br /&gt;
REVDAT   1  16-Nov-06     0                                             NONE   4&lt;br /&gt;
ATOM      1  O           0       3.779  -0.333   0.251  0.00  0.00           O+0&lt;br /&gt;
ATOM      2  C           0       2.568   0.160  -0.050  0.00  0.00           C+0&lt;br /&gt;
ATOM      3  C           0       1.326  -0.540   0.437  0.00  0.00           C+0&lt;br /&gt;
ATOM      4  C           0       0.089   0.222  -0.042  0.00  0.00           C+0&lt;br /&gt;
ATOM      5  C           0      -1.172  -0.489   0.453  0.00  0.00           C+0&lt;br /&gt;
ATOM      6  H           0      -1.124  -0.603   1.536  0.00  0.00           H+0&lt;br /&gt;
ATOM      7  N           0      -1.265  -1.814  -0.174  0.00  0.00           N+0&lt;br /&gt;
ATOM      8  C           0      -2.385   0.327   0.088  0.00  0.00           C+0&lt;br /&gt;
ATOM      9  O           0      -3.155  -0.075  -0.769  0.00  0.00           O-1&lt;br /&gt;
ATOM     10  O           0      -2.598   1.389   0.648  0.00  0.00           O+0&lt;br /&gt;
ATOM     11  O           0       2.473   1.167  -0.713  0.00  0.00           O+0&lt;br /&gt;
ATOM     12  H           0       4.576   0.116  -0.061  0.00  0.00           H+0&lt;br /&gt;
ATOM     13  H           0       1.302  -1.556   0.041  0.00  0.00           H+0&lt;br /&gt;
ATOM     14  H           0       1.332  -0.575   1.527  0.00  0.00           H+0&lt;br /&gt;
ATOM     15  H           0       0.112   1.238   0.354  0.00  0.00           H+0&lt;br /&gt;
ATOM     16  H           0       0.083   0.257  -1.131  0.00  0.00           H+0&lt;br /&gt;
ATOM     17  H           0      -1.307  -1.660  -1.171  0.00  0.00           H+0&lt;br /&gt;
ATOM     18  H           0      -0.392  -2.284   0.010  0.00  0.00           H+0&lt;br /&gt;
CONECT    1    2   12    0    0                                         NONE  23&lt;br /&gt;
CONECT    2    1    3   11    0                                         NONE  24&lt;br /&gt;
CONECT    3    2    4   13   14                                         NONE  25&lt;br /&gt;
CONECT    4    3    5   15   16                                         NONE  26&lt;br /&gt;
CONECT    5    4    6    7    8                                         NONE  27&lt;br /&gt;
CONECT    7    5   17   18    0                                         NONE  28&lt;br /&gt;
CONECT    8    5    9   10    0                                         NONE  29&lt;br /&gt;
CONECT    9    8    0    0    0                                         NONE  30&lt;br /&gt;
CONECT   10    8    0    0    0                                         NONE  31&lt;br /&gt;
CONECT   11    2    0    0    0                                         NONE  32&lt;br /&gt;
END                                                                     NONE  33&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;
&lt;br /&gt;
&lt;br /&gt;
===Spectra===&lt;br /&gt;
[[Image:NMR of MSG.bmp]]&lt;br /&gt;
&lt;br /&gt;
==References &amp;amp; Useful Links==&lt;br /&gt;
Image: http://www.germes-online.com/catalog/48/55/189/257161/monosodium_glutamate.html&lt;br /&gt;
&lt;br /&gt;
http://www.chemicalland21.com/lifescience/foco/MONOSODIUM%20GLUTAMATE.htm&lt;/div&gt;</summary>
		<author><name>Rw305</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It:MSG&amp;diff=5473</id>
		<title>It:MSG</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It:MSG&amp;diff=5473"/>
		<updated>2006-11-16T14:37:03Z</updated>

		<summary type="html">&lt;p&gt;Rw305: /* The Basics */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;==Abstract==&lt;br /&gt;
[[Image:msg2.bmp|centre|300px|Chemical Structure of MSG]]&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;Monosodium Glutamate&#039;&#039;&#039; is more commonly known as &#039;&#039;&#039;MSG&#039;&#039;&#039; and has become the choice chemical for the enhancement of flavour in many foods. It was originally discovered in 1909 by the Ajinomoto Corporation in Japan.&lt;br /&gt;
&lt;br /&gt;
==The Basics==&lt;br /&gt;
{| class=&amp;quot;toccolours&amp;quot; border=&amp;quot;1&amp;quot; style=&amp;quot;float: right; clear: right; margin: 0 0 1em 1em; border-collapse: collapse;&amp;quot;&lt;br /&gt;
! {{chembox header}} | MSG &lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; width=&amp;quot;300&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image:msg.jpg]]&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | General&lt;br /&gt;
|-&lt;br /&gt;
| IUPAC nomenclature|Systematic name&lt;br /&gt;
|2-aminopentanedioic acid&lt;br /&gt;
|-&lt;br /&gt;
| Other names&lt;br /&gt;
|2-aminoglutaric acid, 1-aminopropane-1,&lt;br /&gt;
3-dicarboxylic acid&lt;br /&gt;
|-&lt;br /&gt;
| Chemical formula|Molecular formula]&lt;br /&gt;
|C&amp;lt;sub&amp;gt;5&amp;lt;/sub&amp;gt;H&amp;lt;sub&amp;gt;8&amp;lt;/sub&amp;gt;NNaO&amp;lt;sub&amp;gt;4&amp;lt;/sub&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
|-&lt;br /&gt;
| Molecular Weight&lt;br /&gt;
| 169.11&lt;br /&gt;
|-&lt;br /&gt;
| Appearance&lt;br /&gt;
| White Crystalline Solid&lt;br /&gt;
|-&lt;br /&gt;
| CAS registry number|CAS number&lt;br /&gt;
|142-47-2&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Properties&lt;br /&gt;
|-&lt;br /&gt;
| Melting point&lt;br /&gt;
| 232 °C (505 K)&lt;br /&gt;
|-&lt;br /&gt;
| Related compounds &lt;br /&gt;
| Glutamic Acid&lt;br /&gt;
|-&lt;br /&gt;
| Solubility in Water&lt;br /&gt;
| 100 mg/100ml&lt;br /&gt;
|-&lt;br /&gt;
| pH&lt;br /&gt;
| 7.0&lt;br /&gt;
|-&lt;br /&gt;
| {{chembox header}} | &amp;lt;small&amp;gt;Except where noted otherwise, data are given for&amp;lt;br /&amp;gt; materials in their [[standard state|standard state (at 25&amp;amp;nbsp;°C, 100&amp;amp;nbsp;kPa)]]&amp;lt;br /&amp;gt;[[wikipedia:Chemical infobox|Infobox disclaimer and references]]&amp;lt;/small&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
|}&lt;br /&gt;
MSG,is a sodium salt of the amino acid &#039;&#039;&#039;&#039;&#039;L-glutamic acid&#039;&#039;&#039;&#039;&#039;. It is practically odorless. It is produced by a bacterial fermentation process with starch or molasses as carbon sources and ammonium salts as nitrogen sources (Steffen process). MSG is not a direct taste enhancer but a complex flavour enhancer for gravies, meats, poultry, sauces, and in other combinations. It is also used to enhance the taste of tobacco and has been used medically to treat hepatic coma.&lt;br /&gt;
&lt;br /&gt;
===3D Representation===&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;green&amp;lt;/color&amp;gt;&lt;br /&gt;
&amp;lt;script&amp;gt;zoom 150; 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;&lt;br /&gt;
HEADER    NONAME 16-Nov-06                                              NONE   1&lt;br /&gt;
TITLE                                                                   NONE   2&lt;br /&gt;
AUTHOR    WWW daemon apache                                             NONE   3&lt;br /&gt;
REVDAT   1  16-Nov-06     0                                             NONE   4&lt;br /&gt;
ATOM      1  O           0       3.779  -0.333   0.251  0.00  0.00           O+0&lt;br /&gt;
ATOM      2  C           0       2.568   0.160  -0.050  0.00  0.00           C+0&lt;br /&gt;
ATOM      3  C           0       1.326  -0.540   0.437  0.00  0.00           C+0&lt;br /&gt;
ATOM      4  C           0       0.089   0.222  -0.042  0.00  0.00           C+0&lt;br /&gt;
ATOM      5  C           0      -1.172  -0.489   0.453  0.00  0.00           C+0&lt;br /&gt;
ATOM      6  H           0      -1.124  -0.603   1.536  0.00  0.00           H+0&lt;br /&gt;
ATOM      7  N           0      -1.265  -1.814  -0.174  0.00  0.00           N+0&lt;br /&gt;
ATOM      8  C           0      -2.385   0.327   0.088  0.00  0.00           C+0&lt;br /&gt;
ATOM      9  O           0      -3.155  -0.075  -0.769  0.00  0.00           O-1&lt;br /&gt;
ATOM     10  O           0      -2.598   1.389   0.648  0.00  0.00           O+0&lt;br /&gt;
ATOM     11  O           0       2.473   1.167  -0.713  0.00  0.00           O+0&lt;br /&gt;
ATOM     12  H           0       4.576   0.116  -0.061  0.00  0.00           H+0&lt;br /&gt;
ATOM     13  H           0       1.302  -1.556   0.041  0.00  0.00           H+0&lt;br /&gt;
ATOM     14  H           0       1.332  -0.575   1.527  0.00  0.00           H+0&lt;br /&gt;
ATOM     15  H           0       0.112   1.238   0.354  0.00  0.00           H+0&lt;br /&gt;
ATOM     16  H           0       0.083   0.257  -1.131  0.00  0.00           H+0&lt;br /&gt;
ATOM     17  H           0      -1.307  -1.660  -1.171  0.00  0.00           H+0&lt;br /&gt;
ATOM     18  H           0      -0.392  -2.284   0.010  0.00  0.00           H+0&lt;br /&gt;
CONECT    1    2   12    0    0                                         NONE  23&lt;br /&gt;
CONECT    2    1    3   11    0                                         NONE  24&lt;br /&gt;
CONECT    3    2    4   13   14                                         NONE  25&lt;br /&gt;
CONECT    4    3    5   15   16                                         NONE  26&lt;br /&gt;
CONECT    5    4    6    7    8                                         NONE  27&lt;br /&gt;
CONECT    7    5   17   18    0                                         NONE  28&lt;br /&gt;
CONECT    8    5    9   10    0                                         NONE  29&lt;br /&gt;
CONECT    9    8    0    0    0                                         NONE  30&lt;br /&gt;
CONECT   10    8    0    0    0                                         NONE  31&lt;br /&gt;
CONECT   11    2    0    0    0                                         NONE  32&lt;br /&gt;
END                                                                     NONE  33&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;
&lt;br /&gt;
&lt;br /&gt;
===Spectra===&lt;br /&gt;
&lt;br /&gt;
==References &amp;amp; Useful Links==&lt;br /&gt;
Image: http://www.germes-online.com/catalog/48/55/189/257161/monosodium_glutamate.html&lt;br /&gt;
&lt;br /&gt;
http://www.chemicalland21.com/lifescience/foco/MONOSODIUM%20GLUTAMATE.htm&lt;/div&gt;</summary>
		<author><name>Rw305</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It:MSG&amp;diff=5472</id>
		<title>It:MSG</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It:MSG&amp;diff=5472"/>
		<updated>2006-11-16T14:35:28Z</updated>

		<summary type="html">&lt;p&gt;Rw305: /* Abstract */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;==Abstract==&lt;br /&gt;
[[Image:msg2.bmp|centre|300px|Chemical Structure of MSG]]&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;Monosodium Glutamate&#039;&#039;&#039; is more commonly known as &#039;&#039;&#039;MSG&#039;&#039;&#039; and has become the choice chemical for the enhancement of flavour in many foods. It was originally discovered in 1909 by the Ajinomoto Corporation in Japan.&lt;br /&gt;
&lt;br /&gt;
==The Basics==&lt;br /&gt;
{| class=&amp;quot;toccolours&amp;quot; border=&amp;quot;1&amp;quot; style=&amp;quot;float: right; clear: right; margin: 0 0 1em 1em; border-collapse: collapse;&amp;quot;&lt;br /&gt;
! {{chembox header}} | MSG &lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; width=&amp;quot;300&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image:msg.jpg]]&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | General&lt;br /&gt;
|-&lt;br /&gt;
| IUPAC nomenclature|Systematic name&lt;br /&gt;
|2-aminopentanedioic acid&lt;br /&gt;
|-&lt;br /&gt;
| Other names&lt;br /&gt;
|2-aminoglutaric acid, 1-aminopropane-1,&lt;br /&gt;
3-dicarboxylic acid&lt;br /&gt;
|-&lt;br /&gt;
| Chemical formula|Molecular formula]&lt;br /&gt;
|C&amp;lt;sub&amp;gt;5&amp;lt;/sub&amp;gt;H&amp;lt;sub&amp;gt;8&amp;lt;/sub&amp;gt;NNaO&amp;lt;sub&amp;gt;4&amp;lt;/sub&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
|-&lt;br /&gt;
| Molecular Weight&lt;br /&gt;
| 169.11&lt;br /&gt;
|-&lt;br /&gt;
| Appearance&lt;br /&gt;
| White Crystalline Solid&lt;br /&gt;
|-&lt;br /&gt;
| CAS registry number|CAS number&lt;br /&gt;
|142-47-2&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Properties&lt;br /&gt;
|-&lt;br /&gt;
| Melting point&lt;br /&gt;
| 232 °C (505 K)&lt;br /&gt;
|-&lt;br /&gt;
| Related compounds &lt;br /&gt;
| Glutamic Acid&lt;br /&gt;
|-&lt;br /&gt;
| Solubility in Water&lt;br /&gt;
| 100 mg/100ml&lt;br /&gt;
|-&lt;br /&gt;
| pH&lt;br /&gt;
| 7.0&lt;br /&gt;
|-&lt;br /&gt;
| {{chembox header}} | &amp;lt;small&amp;gt;Except where noted otherwise, data are given for&amp;lt;br /&amp;gt; materials in their [[standard state|standard state (at 25&amp;amp;nbsp;°C, 100&amp;amp;nbsp;kPa)]]&amp;lt;br /&amp;gt;[[wikipedia:Chemical infobox|Infobox disclaimer and references]]&amp;lt;/small&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
|}&lt;br /&gt;
MSG,is a sodium salt of the amino acid &#039;&#039;&#039;&#039;&#039;L-glutamic acid&#039;&#039;&#039;&#039;&#039;. It is practically odorless. It is produced by a bacterial fermentation process with starch or molasses as carbon sources and ammonium salts as nitrogen sources (Steffen process). MSG is not a direct taste enhancer but a complex flavour enhancer for gravies, meats, poultry, sauces, and in other combinations. It is also used to enhance the taste of tobacco and has been used medically to treat hepatic coma.&lt;br /&gt;
&lt;br /&gt;
===3D Representation===&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;green&amp;lt;/color&amp;gt;&lt;br /&gt;
&amp;lt;script&amp;gt;zoom 150; 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;&lt;br /&gt;
HEADER    NONAME 16-Nov-06                                              NONE   1&lt;br /&gt;
TITLE                                                                   NONE   2&lt;br /&gt;
AUTHOR    WWW daemon apache                                             NONE   3&lt;br /&gt;
REVDAT   1  16-Nov-06     0                                             NONE   4&lt;br /&gt;
ATOM      1  O           0       3.779  -0.333   0.251  0.00  0.00           O+0&lt;br /&gt;
ATOM      2  C           0       2.568   0.160  -0.050  0.00  0.00           C+0&lt;br /&gt;
ATOM      3  C           0       1.326  -0.540   0.437  0.00  0.00           C+0&lt;br /&gt;
ATOM      4  C           0       0.089   0.222  -0.042  0.00  0.00           C+0&lt;br /&gt;
ATOM      5  C           0      -1.172  -0.489   0.453  0.00  0.00           C+0&lt;br /&gt;
ATOM      6  H           0      -1.124  -0.603   1.536  0.00  0.00           H+0&lt;br /&gt;
ATOM      7  N           0      -1.265  -1.814  -0.174  0.00  0.00           N+0&lt;br /&gt;
ATOM      8  C           0      -2.385   0.327   0.088  0.00  0.00           C+0&lt;br /&gt;
ATOM      9  O           0      -3.155  -0.075  -0.769  0.00  0.00           O-1&lt;br /&gt;
ATOM     10  O           0      -2.598   1.389   0.648  0.00  0.00           O+0&lt;br /&gt;
ATOM     11  O           0       2.473   1.167  -0.713  0.00  0.00           O+0&lt;br /&gt;
ATOM     12  H           0       4.576   0.116  -0.061  0.00  0.00           H+0&lt;br /&gt;
ATOM     13  H           0       1.302  -1.556   0.041  0.00  0.00           H+0&lt;br /&gt;
ATOM     14  H           0       1.332  -0.575   1.527  0.00  0.00           H+0&lt;br /&gt;
ATOM     15  H           0       0.112   1.238   0.354  0.00  0.00           H+0&lt;br /&gt;
ATOM     16  H           0       0.083   0.257  -1.131  0.00  0.00           H+0&lt;br /&gt;
ATOM     17  H           0      -1.307  -1.660  -1.171  0.00  0.00           H+0&lt;br /&gt;
ATOM     18  H           0      -0.392  -2.284   0.010  0.00  0.00           H+0&lt;br /&gt;
CONECT    1    2   12    0    0                                         NONE  23&lt;br /&gt;
CONECT    2    1    3   11    0                                         NONE  24&lt;br /&gt;
CONECT    3    2    4   13   14                                         NONE  25&lt;br /&gt;
CONECT    4    3    5   15   16                                         NONE  26&lt;br /&gt;
CONECT    5    4    6    7    8                                         NONE  27&lt;br /&gt;
CONECT    7    5   17   18    0                                         NONE  28&lt;br /&gt;
CONECT    8    5    9   10    0                                         NONE  29&lt;br /&gt;
CONECT    9    8    0    0    0                                         NONE  30&lt;br /&gt;
CONECT   10    8    0    0    0                                         NONE  31&lt;br /&gt;
CONECT   11    2    0    0    0                                         NONE  32&lt;br /&gt;
END                                                                     NONE  33&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;
&lt;br /&gt;
==References &amp;amp; Useful Links==&lt;br /&gt;
Image: http://www.germes-online.com/catalog/48/55/189/257161/monosodium_glutamate.html&lt;br /&gt;
&lt;br /&gt;
http://www.chemicalland21.com/lifescience/foco/MONOSODIUM%20GLUTAMATE.htm&lt;/div&gt;</summary>
		<author><name>Rw305</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=File:Msg2.bmp&amp;diff=5471</id>
		<title>File:Msg2.bmp</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=File:Msg2.bmp&amp;diff=5471"/>
		<updated>2006-11-16T14:32:23Z</updated>

		<summary type="html">&lt;p&gt;Rw305: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;/div&gt;</summary>
		<author><name>Rw305</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It:MSG&amp;diff=5470</id>
		<title>It:MSG</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It:MSG&amp;diff=5470"/>
		<updated>2006-11-16T14:32:12Z</updated>

		<summary type="html">&lt;p&gt;Rw305: /* Abstract */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;==Abstract==&lt;br /&gt;
[[Image:msg2.bmp|centre|Chemical Structure of MSG]]&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;Monosodium Glutamate&#039;&#039;&#039; is more commonly known as &#039;&#039;&#039;MSG&#039;&#039;&#039; and has become the choice chemical for the enhancement of flavour in many foods. It was originally discovered in 1909 by the Ajinomoto Corporation in Japan.&lt;br /&gt;
&lt;br /&gt;
==The Basics==&lt;br /&gt;
{| class=&amp;quot;toccolours&amp;quot; border=&amp;quot;1&amp;quot; style=&amp;quot;float: right; clear: right; margin: 0 0 1em 1em; border-collapse: collapse;&amp;quot;&lt;br /&gt;
! {{chembox header}} | MSG &lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; width=&amp;quot;300&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image:msg.jpg]]&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | General&lt;br /&gt;
|-&lt;br /&gt;
| IUPAC nomenclature|Systematic name&lt;br /&gt;
|2-aminopentanedioic acid&lt;br /&gt;
|-&lt;br /&gt;
| Other names&lt;br /&gt;
|2-aminoglutaric acid, 1-aminopropane-1,&lt;br /&gt;
3-dicarboxylic acid&lt;br /&gt;
|-&lt;br /&gt;
| Chemical formula|Molecular formula]&lt;br /&gt;
|C&amp;lt;sub&amp;gt;5&amp;lt;/sub&amp;gt;H&amp;lt;sub&amp;gt;8&amp;lt;/sub&amp;gt;NNaO&amp;lt;sub&amp;gt;4&amp;lt;/sub&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
|-&lt;br /&gt;
| Molecular Weight&lt;br /&gt;
| 169.11&lt;br /&gt;
|-&lt;br /&gt;
| Appearance&lt;br /&gt;
| White Crystalline Solid&lt;br /&gt;
|-&lt;br /&gt;
| CAS registry number|CAS number&lt;br /&gt;
|142-47-2&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Properties&lt;br /&gt;
|-&lt;br /&gt;
| Melting point&lt;br /&gt;
| 232 °C (505 K)&lt;br /&gt;
|-&lt;br /&gt;
| Related compounds &lt;br /&gt;
| Glutamic Acid&lt;br /&gt;
|-&lt;br /&gt;
| Solubility in Water&lt;br /&gt;
| 100 mg/100ml&lt;br /&gt;
|-&lt;br /&gt;
| pH&lt;br /&gt;
| 7.0&lt;br /&gt;
|-&lt;br /&gt;
| {{chembox header}} | &amp;lt;small&amp;gt;Except where noted otherwise, data are given for&amp;lt;br /&amp;gt; materials in their [[standard state|standard state (at 25&amp;amp;nbsp;°C, 100&amp;amp;nbsp;kPa)]]&amp;lt;br /&amp;gt;[[wikipedia:Chemical infobox|Infobox disclaimer and references]]&amp;lt;/small&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
|}&lt;br /&gt;
MSG,is a sodium salt of the amino acid &#039;&#039;&#039;&#039;&#039;L-glutamic acid&#039;&#039;&#039;&#039;&#039;. It is practically odorless. It is produced by a bacterial fermentation process with starch or molasses as carbon sources and ammonium salts as nitrogen sources (Steffen process). MSG is not a direct taste enhancer but a complex flavour enhancer for gravies, meats, poultry, sauces, and in other combinations. It is also used to enhance the taste of tobacco and has been used medically to treat hepatic coma.&lt;br /&gt;
&lt;br /&gt;
===3D Representation===&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;green&amp;lt;/color&amp;gt;&lt;br /&gt;
&amp;lt;script&amp;gt;zoom 150; 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;&lt;br /&gt;
HEADER    NONAME 16-Nov-06                                              NONE   1&lt;br /&gt;
TITLE                                                                   NONE   2&lt;br /&gt;
AUTHOR    WWW daemon apache                                             NONE   3&lt;br /&gt;
REVDAT   1  16-Nov-06     0                                             NONE   4&lt;br /&gt;
ATOM      1  O           0       3.779  -0.333   0.251  0.00  0.00           O+0&lt;br /&gt;
ATOM      2  C           0       2.568   0.160  -0.050  0.00  0.00           C+0&lt;br /&gt;
ATOM      3  C           0       1.326  -0.540   0.437  0.00  0.00           C+0&lt;br /&gt;
ATOM      4  C           0       0.089   0.222  -0.042  0.00  0.00           C+0&lt;br /&gt;
ATOM      5  C           0      -1.172  -0.489   0.453  0.00  0.00           C+0&lt;br /&gt;
ATOM      6  H           0      -1.124  -0.603   1.536  0.00  0.00           H+0&lt;br /&gt;
ATOM      7  N           0      -1.265  -1.814  -0.174  0.00  0.00           N+0&lt;br /&gt;
ATOM      8  C           0      -2.385   0.327   0.088  0.00  0.00           C+0&lt;br /&gt;
ATOM      9  O           0      -3.155  -0.075  -0.769  0.00  0.00           O-1&lt;br /&gt;
ATOM     10  O           0      -2.598   1.389   0.648  0.00  0.00           O+0&lt;br /&gt;
ATOM     11  O           0       2.473   1.167  -0.713  0.00  0.00           O+0&lt;br /&gt;
ATOM     12  H           0       4.576   0.116  -0.061  0.00  0.00           H+0&lt;br /&gt;
ATOM     13  H           0       1.302  -1.556   0.041  0.00  0.00           H+0&lt;br /&gt;
ATOM     14  H           0       1.332  -0.575   1.527  0.00  0.00           H+0&lt;br /&gt;
ATOM     15  H           0       0.112   1.238   0.354  0.00  0.00           H+0&lt;br /&gt;
ATOM     16  H           0       0.083   0.257  -1.131  0.00  0.00           H+0&lt;br /&gt;
ATOM     17  H           0      -1.307  -1.660  -1.171  0.00  0.00           H+0&lt;br /&gt;
ATOM     18  H           0      -0.392  -2.284   0.010  0.00  0.00           H+0&lt;br /&gt;
CONECT    1    2   12    0    0                                         NONE  23&lt;br /&gt;
CONECT    2    1    3   11    0                                         NONE  24&lt;br /&gt;
CONECT    3    2    4   13   14                                         NONE  25&lt;br /&gt;
CONECT    4    3    5   15   16                                         NONE  26&lt;br /&gt;
CONECT    5    4    6    7    8                                         NONE  27&lt;br /&gt;
CONECT    7    5   17   18    0                                         NONE  28&lt;br /&gt;
CONECT    8    5    9   10    0                                         NONE  29&lt;br /&gt;
CONECT    9    8    0    0    0                                         NONE  30&lt;br /&gt;
CONECT   10    8    0    0    0                                         NONE  31&lt;br /&gt;
CONECT   11    2    0    0    0                                         NONE  32&lt;br /&gt;
END                                                                     NONE  33&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;
&lt;br /&gt;
==References &amp;amp; Useful Links==&lt;br /&gt;
Image: http://www.germes-online.com/catalog/48/55/189/257161/monosodium_glutamate.html&lt;br /&gt;
&lt;br /&gt;
http://www.chemicalland21.com/lifescience/foco/MONOSODIUM%20GLUTAMATE.htm&lt;/div&gt;</summary>
		<author><name>Rw305</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It:MSG&amp;diff=5469</id>
		<title>It:MSG</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It:MSG&amp;diff=5469"/>
		<updated>2006-11-16T14:31:34Z</updated>

		<summary type="html">&lt;p&gt;Rw305: /* Abstract */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;==Abstract==&lt;br /&gt;
&amp;lt;align centre&amp;gt;[[Image:msg2.bmp]]&amp;lt;/align centre&amp;gt;&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;Monosodium Glutamate&#039;&#039;&#039; is more commonly known as &#039;&#039;&#039;MSG&#039;&#039;&#039; and has become the choice chemical for the enhancement of flavour in many foods. It was originally discovered in 1909 by the Ajinomoto Corporation in Japan.&lt;br /&gt;
&lt;br /&gt;
==The Basics==&lt;br /&gt;
{| class=&amp;quot;toccolours&amp;quot; border=&amp;quot;1&amp;quot; style=&amp;quot;float: right; clear: right; margin: 0 0 1em 1em; border-collapse: collapse;&amp;quot;&lt;br /&gt;
! {{chembox header}} | MSG &lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; width=&amp;quot;300&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image:msg.jpg]]&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | General&lt;br /&gt;
|-&lt;br /&gt;
| IUPAC nomenclature|Systematic name&lt;br /&gt;
|2-aminopentanedioic acid&lt;br /&gt;
|-&lt;br /&gt;
| Other names&lt;br /&gt;
|2-aminoglutaric acid, 1-aminopropane-1,&lt;br /&gt;
3-dicarboxylic acid&lt;br /&gt;
|-&lt;br /&gt;
| Chemical formula|Molecular formula]&lt;br /&gt;
|C&amp;lt;sub&amp;gt;5&amp;lt;/sub&amp;gt;H&amp;lt;sub&amp;gt;8&amp;lt;/sub&amp;gt;NNaO&amp;lt;sub&amp;gt;4&amp;lt;/sub&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
|-&lt;br /&gt;
| Molecular Weight&lt;br /&gt;
| 169.11&lt;br /&gt;
|-&lt;br /&gt;
| Appearance&lt;br /&gt;
| White Crystalline Solid&lt;br /&gt;
|-&lt;br /&gt;
| CAS registry number|CAS number&lt;br /&gt;
|142-47-2&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Properties&lt;br /&gt;
|-&lt;br /&gt;
| Melting point&lt;br /&gt;
| 232 °C (505 K)&lt;br /&gt;
|-&lt;br /&gt;
| Related compounds &lt;br /&gt;
| Glutamic Acid&lt;br /&gt;
|-&lt;br /&gt;
| Solubility in Water&lt;br /&gt;
| 100 mg/100ml&lt;br /&gt;
|-&lt;br /&gt;
| pH&lt;br /&gt;
| 7.0&lt;br /&gt;
|-&lt;br /&gt;
| {{chembox header}} | &amp;lt;small&amp;gt;Except where noted otherwise, data are given for&amp;lt;br /&amp;gt; materials in their [[standard state|standard state (at 25&amp;amp;nbsp;°C, 100&amp;amp;nbsp;kPa)]]&amp;lt;br /&amp;gt;[[wikipedia:Chemical infobox|Infobox disclaimer and references]]&amp;lt;/small&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
|}&lt;br /&gt;
MSG,is a sodium salt of the amino acid &#039;&#039;&#039;&#039;&#039;L-glutamic acid&#039;&#039;&#039;&#039;&#039;. It is practically odorless. It is produced by a bacterial fermentation process with starch or molasses as carbon sources and ammonium salts as nitrogen sources (Steffen process). MSG is not a direct taste enhancer but a complex flavour enhancer for gravies, meats, poultry, sauces, and in other combinations. It is also used to enhance the taste of tobacco and has been used medically to treat hepatic coma.&lt;br /&gt;
&lt;br /&gt;
===3D Representation===&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;green&amp;lt;/color&amp;gt;&lt;br /&gt;
&amp;lt;script&amp;gt;zoom 150; 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;&lt;br /&gt;
HEADER    NONAME 16-Nov-06                                              NONE   1&lt;br /&gt;
TITLE                                                                   NONE   2&lt;br /&gt;
AUTHOR    WWW daemon apache                                             NONE   3&lt;br /&gt;
REVDAT   1  16-Nov-06     0                                             NONE   4&lt;br /&gt;
ATOM      1  O           0       3.779  -0.333   0.251  0.00  0.00           O+0&lt;br /&gt;
ATOM      2  C           0       2.568   0.160  -0.050  0.00  0.00           C+0&lt;br /&gt;
ATOM      3  C           0       1.326  -0.540   0.437  0.00  0.00           C+0&lt;br /&gt;
ATOM      4  C           0       0.089   0.222  -0.042  0.00  0.00           C+0&lt;br /&gt;
ATOM      5  C           0      -1.172  -0.489   0.453  0.00  0.00           C+0&lt;br /&gt;
ATOM      6  H           0      -1.124  -0.603   1.536  0.00  0.00           H+0&lt;br /&gt;
ATOM      7  N           0      -1.265  -1.814  -0.174  0.00  0.00           N+0&lt;br /&gt;
ATOM      8  C           0      -2.385   0.327   0.088  0.00  0.00           C+0&lt;br /&gt;
ATOM      9  O           0      -3.155  -0.075  -0.769  0.00  0.00           O-1&lt;br /&gt;
ATOM     10  O           0      -2.598   1.389   0.648  0.00  0.00           O+0&lt;br /&gt;
ATOM     11  O           0       2.473   1.167  -0.713  0.00  0.00           O+0&lt;br /&gt;
ATOM     12  H           0       4.576   0.116  -0.061  0.00  0.00           H+0&lt;br /&gt;
ATOM     13  H           0       1.302  -1.556   0.041  0.00  0.00           H+0&lt;br /&gt;
ATOM     14  H           0       1.332  -0.575   1.527  0.00  0.00           H+0&lt;br /&gt;
ATOM     15  H           0       0.112   1.238   0.354  0.00  0.00           H+0&lt;br /&gt;
ATOM     16  H           0       0.083   0.257  -1.131  0.00  0.00           H+0&lt;br /&gt;
ATOM     17  H           0      -1.307  -1.660  -1.171  0.00  0.00           H+0&lt;br /&gt;
ATOM     18  H           0      -0.392  -2.284   0.010  0.00  0.00           H+0&lt;br /&gt;
CONECT    1    2   12    0    0                                         NONE  23&lt;br /&gt;
CONECT    2    1    3   11    0                                         NONE  24&lt;br /&gt;
CONECT    3    2    4   13   14                                         NONE  25&lt;br /&gt;
CONECT    4    3    5   15   16                                         NONE  26&lt;br /&gt;
CONECT    5    4    6    7    8                                         NONE  27&lt;br /&gt;
CONECT    7    5   17   18    0                                         NONE  28&lt;br /&gt;
CONECT    8    5    9   10    0                                         NONE  29&lt;br /&gt;
CONECT    9    8    0    0    0                                         NONE  30&lt;br /&gt;
CONECT   10    8    0    0    0                                         NONE  31&lt;br /&gt;
CONECT   11    2    0    0    0                                         NONE  32&lt;br /&gt;
END                                                                     NONE  33&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;
&lt;br /&gt;
==References &amp;amp; Useful Links==&lt;br /&gt;
Image: http://www.germes-online.com/catalog/48/55/189/257161/monosodium_glutamate.html&lt;br /&gt;
&lt;br /&gt;
http://www.chemicalland21.com/lifescience/foco/MONOSODIUM%20GLUTAMATE.htm&lt;/div&gt;</summary>
		<author><name>Rw305</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It:MSG&amp;diff=5468</id>
		<title>It:MSG</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It:MSG&amp;diff=5468"/>
		<updated>2006-11-16T14:31:12Z</updated>

		<summary type="html">&lt;p&gt;Rw305: /* Abstract */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;==Abstract==&lt;br /&gt;
&amp;lt;align centre&amp;gt;[[Image:msg2.jpg]]&amp;lt;/align centre&amp;gt;&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;Monosodium Glutamate&#039;&#039;&#039; is more commonly known as &#039;&#039;&#039;MSG&#039;&#039;&#039; and has become the choice chemical for the enhancement of flavour in many foods. It was originally discovered in 1909 by the Ajinomoto Corporation in Japan.&lt;br /&gt;
&lt;br /&gt;
==The Basics==&lt;br /&gt;
{| class=&amp;quot;toccolours&amp;quot; border=&amp;quot;1&amp;quot; style=&amp;quot;float: right; clear: right; margin: 0 0 1em 1em; border-collapse: collapse;&amp;quot;&lt;br /&gt;
! {{chembox header}} | MSG &lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; width=&amp;quot;300&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image:msg.jpg]]&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | General&lt;br /&gt;
|-&lt;br /&gt;
| IUPAC nomenclature|Systematic name&lt;br /&gt;
|2-aminopentanedioic acid&lt;br /&gt;
|-&lt;br /&gt;
| Other names&lt;br /&gt;
|2-aminoglutaric acid, 1-aminopropane-1,&lt;br /&gt;
3-dicarboxylic acid&lt;br /&gt;
|-&lt;br /&gt;
| Chemical formula|Molecular formula]&lt;br /&gt;
|C&amp;lt;sub&amp;gt;5&amp;lt;/sub&amp;gt;H&amp;lt;sub&amp;gt;8&amp;lt;/sub&amp;gt;NNaO&amp;lt;sub&amp;gt;4&amp;lt;/sub&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
|-&lt;br /&gt;
| Molecular Weight&lt;br /&gt;
| 169.11&lt;br /&gt;
|-&lt;br /&gt;
| Appearance&lt;br /&gt;
| White Crystalline Solid&lt;br /&gt;
|-&lt;br /&gt;
| CAS registry number|CAS number&lt;br /&gt;
|142-47-2&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Properties&lt;br /&gt;
|-&lt;br /&gt;
| Melting point&lt;br /&gt;
| 232 °C (505 K)&lt;br /&gt;
|-&lt;br /&gt;
| Related compounds &lt;br /&gt;
| Glutamic Acid&lt;br /&gt;
|-&lt;br /&gt;
| Solubility in Water&lt;br /&gt;
| 100 mg/100ml&lt;br /&gt;
|-&lt;br /&gt;
| pH&lt;br /&gt;
| 7.0&lt;br /&gt;
|-&lt;br /&gt;
| {{chembox header}} | &amp;lt;small&amp;gt;Except where noted otherwise, data are given for&amp;lt;br /&amp;gt; materials in their [[standard state|standard state (at 25&amp;amp;nbsp;°C, 100&amp;amp;nbsp;kPa)]]&amp;lt;br /&amp;gt;[[wikipedia:Chemical infobox|Infobox disclaimer and references]]&amp;lt;/small&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
|}&lt;br /&gt;
MSG,is a sodium salt of the amino acid &#039;&#039;&#039;&#039;&#039;L-glutamic acid&#039;&#039;&#039;&#039;&#039;. It is practically odorless. It is produced by a bacterial fermentation process with starch or molasses as carbon sources and ammonium salts as nitrogen sources (Steffen process). MSG is not a direct taste enhancer but a complex flavour enhancer for gravies, meats, poultry, sauces, and in other combinations. It is also used to enhance the taste of tobacco and has been used medically to treat hepatic coma.&lt;br /&gt;
&lt;br /&gt;
===3D Representation===&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;green&amp;lt;/color&amp;gt;&lt;br /&gt;
&amp;lt;script&amp;gt;zoom 150; 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;&lt;br /&gt;
HEADER    NONAME 16-Nov-06                                              NONE   1&lt;br /&gt;
TITLE                                                                   NONE   2&lt;br /&gt;
AUTHOR    WWW daemon apache                                             NONE   3&lt;br /&gt;
REVDAT   1  16-Nov-06     0                                             NONE   4&lt;br /&gt;
ATOM      1  O           0       3.779  -0.333   0.251  0.00  0.00           O+0&lt;br /&gt;
ATOM      2  C           0       2.568   0.160  -0.050  0.00  0.00           C+0&lt;br /&gt;
ATOM      3  C           0       1.326  -0.540   0.437  0.00  0.00           C+0&lt;br /&gt;
ATOM      4  C           0       0.089   0.222  -0.042  0.00  0.00           C+0&lt;br /&gt;
ATOM      5  C           0      -1.172  -0.489   0.453  0.00  0.00           C+0&lt;br /&gt;
ATOM      6  H           0      -1.124  -0.603   1.536  0.00  0.00           H+0&lt;br /&gt;
ATOM      7  N           0      -1.265  -1.814  -0.174  0.00  0.00           N+0&lt;br /&gt;
ATOM      8  C           0      -2.385   0.327   0.088  0.00  0.00           C+0&lt;br /&gt;
ATOM      9  O           0      -3.155  -0.075  -0.769  0.00  0.00           O-1&lt;br /&gt;
ATOM     10  O           0      -2.598   1.389   0.648  0.00  0.00           O+0&lt;br /&gt;
ATOM     11  O           0       2.473   1.167  -0.713  0.00  0.00           O+0&lt;br /&gt;
ATOM     12  H           0       4.576   0.116  -0.061  0.00  0.00           H+0&lt;br /&gt;
ATOM     13  H           0       1.302  -1.556   0.041  0.00  0.00           H+0&lt;br /&gt;
ATOM     14  H           0       1.332  -0.575   1.527  0.00  0.00           H+0&lt;br /&gt;
ATOM     15  H           0       0.112   1.238   0.354  0.00  0.00           H+0&lt;br /&gt;
ATOM     16  H           0       0.083   0.257  -1.131  0.00  0.00           H+0&lt;br /&gt;
ATOM     17  H           0      -1.307  -1.660  -1.171  0.00  0.00           H+0&lt;br /&gt;
ATOM     18  H           0      -0.392  -2.284   0.010  0.00  0.00           H+0&lt;br /&gt;
CONECT    1    2   12    0    0                                         NONE  23&lt;br /&gt;
CONECT    2    1    3   11    0                                         NONE  24&lt;br /&gt;
CONECT    3    2    4   13   14                                         NONE  25&lt;br /&gt;
CONECT    4    3    5   15   16                                         NONE  26&lt;br /&gt;
CONECT    5    4    6    7    8                                         NONE  27&lt;br /&gt;
CONECT    7    5   17   18    0                                         NONE  28&lt;br /&gt;
CONECT    8    5    9   10    0                                         NONE  29&lt;br /&gt;
CONECT    9    8    0    0    0                                         NONE  30&lt;br /&gt;
CONECT   10    8    0    0    0                                         NONE  31&lt;br /&gt;
CONECT   11    2    0    0    0                                         NONE  32&lt;br /&gt;
END                                                                     NONE  33&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;
&lt;br /&gt;
==References &amp;amp; Useful Links==&lt;br /&gt;
Image: http://www.germes-online.com/catalog/48/55/189/257161/monosodium_glutamate.html&lt;br /&gt;
&lt;br /&gt;
http://www.chemicalland21.com/lifescience/foco/MONOSODIUM%20GLUTAMATE.htm&lt;/div&gt;</summary>
		<author><name>Rw305</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It:MSG&amp;diff=5467</id>
		<title>It:MSG</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It:MSG&amp;diff=5467"/>
		<updated>2006-11-16T14:30:50Z</updated>

		<summary type="html">&lt;p&gt;Rw305: /* Abstract */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;==Abstract==&lt;br /&gt;
[[Image:msg2.jpg]]&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;Monosodium Glutamate&#039;&#039;&#039; is more commonly known as &#039;&#039;&#039;MSG&#039;&#039;&#039; and has become the choice chemical for the enhancement of flavour in many foods. It was originally discovered in 1909 by the Ajinomoto Corporation in Japan.&lt;br /&gt;
&lt;br /&gt;
==The Basics==&lt;br /&gt;
{| class=&amp;quot;toccolours&amp;quot; border=&amp;quot;1&amp;quot; style=&amp;quot;float: right; clear: right; margin: 0 0 1em 1em; border-collapse: collapse;&amp;quot;&lt;br /&gt;
! {{chembox header}} | MSG &lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; width=&amp;quot;300&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image:msg.jpg]]&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | General&lt;br /&gt;
|-&lt;br /&gt;
| IUPAC nomenclature|Systematic name&lt;br /&gt;
|2-aminopentanedioic acid&lt;br /&gt;
|-&lt;br /&gt;
| Other names&lt;br /&gt;
|2-aminoglutaric acid, 1-aminopropane-1,&lt;br /&gt;
3-dicarboxylic acid&lt;br /&gt;
|-&lt;br /&gt;
| Chemical formula|Molecular formula]&lt;br /&gt;
|C&amp;lt;sub&amp;gt;5&amp;lt;/sub&amp;gt;H&amp;lt;sub&amp;gt;8&amp;lt;/sub&amp;gt;NNaO&amp;lt;sub&amp;gt;4&amp;lt;/sub&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
|-&lt;br /&gt;
| Molecular Weight&lt;br /&gt;
| 169.11&lt;br /&gt;
|-&lt;br /&gt;
| Appearance&lt;br /&gt;
| White Crystalline Solid&lt;br /&gt;
|-&lt;br /&gt;
| CAS registry number|CAS number&lt;br /&gt;
|142-47-2&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Properties&lt;br /&gt;
|-&lt;br /&gt;
| Melting point&lt;br /&gt;
| 232 °C (505 K)&lt;br /&gt;
|-&lt;br /&gt;
| Related compounds &lt;br /&gt;
| Glutamic Acid&lt;br /&gt;
|-&lt;br /&gt;
| Solubility in Water&lt;br /&gt;
| 100 mg/100ml&lt;br /&gt;
|-&lt;br /&gt;
| pH&lt;br /&gt;
| 7.0&lt;br /&gt;
|-&lt;br /&gt;
| {{chembox header}} | &amp;lt;small&amp;gt;Except where noted otherwise, data are given for&amp;lt;br /&amp;gt; materials in their [[standard state|standard state (at 25&amp;amp;nbsp;°C, 100&amp;amp;nbsp;kPa)]]&amp;lt;br /&amp;gt;[[wikipedia:Chemical infobox|Infobox disclaimer and references]]&amp;lt;/small&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
|}&lt;br /&gt;
MSG,is a sodium salt of the amino acid &#039;&#039;&#039;&#039;&#039;L-glutamic acid&#039;&#039;&#039;&#039;&#039;. It is practically odorless. It is produced by a bacterial fermentation process with starch or molasses as carbon sources and ammonium salts as nitrogen sources (Steffen process). MSG is not a direct taste enhancer but a complex flavour enhancer for gravies, meats, poultry, sauces, and in other combinations. It is also used to enhance the taste of tobacco and has been used medically to treat hepatic coma.&lt;br /&gt;
&lt;br /&gt;
===3D Representation===&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;green&amp;lt;/color&amp;gt;&lt;br /&gt;
&amp;lt;script&amp;gt;zoom 150; 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;&lt;br /&gt;
HEADER    NONAME 16-Nov-06                                              NONE   1&lt;br /&gt;
TITLE                                                                   NONE   2&lt;br /&gt;
AUTHOR    WWW daemon apache                                             NONE   3&lt;br /&gt;
REVDAT   1  16-Nov-06     0                                             NONE   4&lt;br /&gt;
ATOM      1  O           0       3.779  -0.333   0.251  0.00  0.00           O+0&lt;br /&gt;
ATOM      2  C           0       2.568   0.160  -0.050  0.00  0.00           C+0&lt;br /&gt;
ATOM      3  C           0       1.326  -0.540   0.437  0.00  0.00           C+0&lt;br /&gt;
ATOM      4  C           0       0.089   0.222  -0.042  0.00  0.00           C+0&lt;br /&gt;
ATOM      5  C           0      -1.172  -0.489   0.453  0.00  0.00           C+0&lt;br /&gt;
ATOM      6  H           0      -1.124  -0.603   1.536  0.00  0.00           H+0&lt;br /&gt;
ATOM      7  N           0      -1.265  -1.814  -0.174  0.00  0.00           N+0&lt;br /&gt;
ATOM      8  C           0      -2.385   0.327   0.088  0.00  0.00           C+0&lt;br /&gt;
ATOM      9  O           0      -3.155  -0.075  -0.769  0.00  0.00           O-1&lt;br /&gt;
ATOM     10  O           0      -2.598   1.389   0.648  0.00  0.00           O+0&lt;br /&gt;
ATOM     11  O           0       2.473   1.167  -0.713  0.00  0.00           O+0&lt;br /&gt;
ATOM     12  H           0       4.576   0.116  -0.061  0.00  0.00           H+0&lt;br /&gt;
ATOM     13  H           0       1.302  -1.556   0.041  0.00  0.00           H+0&lt;br /&gt;
ATOM     14  H           0       1.332  -0.575   1.527  0.00  0.00           H+0&lt;br /&gt;
ATOM     15  H           0       0.112   1.238   0.354  0.00  0.00           H+0&lt;br /&gt;
ATOM     16  H           0       0.083   0.257  -1.131  0.00  0.00           H+0&lt;br /&gt;
ATOM     17  H           0      -1.307  -1.660  -1.171  0.00  0.00           H+0&lt;br /&gt;
ATOM     18  H           0      -0.392  -2.284   0.010  0.00  0.00           H+0&lt;br /&gt;
CONECT    1    2   12    0    0                                         NONE  23&lt;br /&gt;
CONECT    2    1    3   11    0                                         NONE  24&lt;br /&gt;
CONECT    3    2    4   13   14                                         NONE  25&lt;br /&gt;
CONECT    4    3    5   15   16                                         NONE  26&lt;br /&gt;
CONECT    5    4    6    7    8                                         NONE  27&lt;br /&gt;
CONECT    7    5   17   18    0                                         NONE  28&lt;br /&gt;
CONECT    8    5    9   10    0                                         NONE  29&lt;br /&gt;
CONECT    9    8    0    0    0                                         NONE  30&lt;br /&gt;
CONECT   10    8    0    0    0                                         NONE  31&lt;br /&gt;
CONECT   11    2    0    0    0                                         NONE  32&lt;br /&gt;
END                                                                     NONE  33&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;
&lt;br /&gt;
==References &amp;amp; Useful Links==&lt;br /&gt;
Image: http://www.germes-online.com/catalog/48/55/189/257161/monosodium_glutamate.html&lt;br /&gt;
&lt;br /&gt;
http://www.chemicalland21.com/lifescience/foco/MONOSODIUM%20GLUTAMATE.htm&lt;/div&gt;</summary>
		<author><name>Rw305</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=File:Msg2.jpg&amp;diff=5466</id>
		<title>File:Msg2.jpg</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=File:Msg2.jpg&amp;diff=5466"/>
		<updated>2006-11-16T14:30:39Z</updated>

		<summary type="html">&lt;p&gt;Rw305: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;/div&gt;</summary>
		<author><name>Rw305</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It:MSG&amp;diff=5465</id>
		<title>It:MSG</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It:MSG&amp;diff=5465"/>
		<updated>2006-11-16T14:28:48Z</updated>

		<summary type="html">&lt;p&gt;Rw305: /* Abstract */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;==Abstract==&lt;br /&gt;
[[Image:msg2.jpg]]&lt;br /&gt;
&#039;&#039;&#039;Monosodium Glutamate&#039;&#039;&#039; is more commonly known as &#039;&#039;&#039;MSG&#039;&#039;&#039; and has become the choice chemical for the enhancement of flavour in many foods. It was originally discovered in 1909 by the Ajinomoto Corporation in Japan.&lt;br /&gt;
&lt;br /&gt;
==The Basics==&lt;br /&gt;
{| class=&amp;quot;toccolours&amp;quot; border=&amp;quot;1&amp;quot; style=&amp;quot;float: right; clear: right; margin: 0 0 1em 1em; border-collapse: collapse;&amp;quot;&lt;br /&gt;
! {{chembox header}} | MSG &lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; width=&amp;quot;300&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image:msg.jpg]]&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | General&lt;br /&gt;
|-&lt;br /&gt;
| IUPAC nomenclature|Systematic name&lt;br /&gt;
|2-aminopentanedioic acid&lt;br /&gt;
|-&lt;br /&gt;
| Other names&lt;br /&gt;
|2-aminoglutaric acid, 1-aminopropane-1,&lt;br /&gt;
3-dicarboxylic acid&lt;br /&gt;
|-&lt;br /&gt;
| Chemical formula|Molecular formula]&lt;br /&gt;
|C&amp;lt;sub&amp;gt;5&amp;lt;/sub&amp;gt;H&amp;lt;sub&amp;gt;8&amp;lt;/sub&amp;gt;NNaO&amp;lt;sub&amp;gt;4&amp;lt;/sub&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
|-&lt;br /&gt;
| Molecular Weight&lt;br /&gt;
| 169.11&lt;br /&gt;
|-&lt;br /&gt;
| Appearance&lt;br /&gt;
| White Crystalline Solid&lt;br /&gt;
|-&lt;br /&gt;
| CAS registry number|CAS number&lt;br /&gt;
|142-47-2&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Properties&lt;br /&gt;
|-&lt;br /&gt;
| Melting point&lt;br /&gt;
| 232 °C (505 K)&lt;br /&gt;
|-&lt;br /&gt;
| Related compounds &lt;br /&gt;
| Glutamic Acid&lt;br /&gt;
|-&lt;br /&gt;
| Solubility in Water&lt;br /&gt;
| 100 mg/100ml&lt;br /&gt;
|-&lt;br /&gt;
| pH&lt;br /&gt;
| 7.0&lt;br /&gt;
|-&lt;br /&gt;
| {{chembox header}} | &amp;lt;small&amp;gt;Except where noted otherwise, data are given for&amp;lt;br /&amp;gt; materials in their [[standard state|standard state (at 25&amp;amp;nbsp;°C, 100&amp;amp;nbsp;kPa)]]&amp;lt;br /&amp;gt;[[wikipedia:Chemical infobox|Infobox disclaimer and references]]&amp;lt;/small&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
|}&lt;br /&gt;
MSG,is a sodium salt of the amino acid &#039;&#039;&#039;&#039;&#039;L-glutamic acid&#039;&#039;&#039;&#039;&#039;. It is practically odorless. It is produced by a bacterial fermentation process with starch or molasses as carbon sources and ammonium salts as nitrogen sources (Steffen process). MSG is not a direct taste enhancer but a complex flavour enhancer for gravies, meats, poultry, sauces, and in other combinations. It is also used to enhance the taste of tobacco and has been used medically to treat hepatic coma.&lt;br /&gt;
&lt;br /&gt;
===3D Representation===&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;green&amp;lt;/color&amp;gt;&lt;br /&gt;
&amp;lt;script&amp;gt;zoom 150; 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;&lt;br /&gt;
HEADER    NONAME 16-Nov-06                                              NONE   1&lt;br /&gt;
TITLE                                                                   NONE   2&lt;br /&gt;
AUTHOR    WWW daemon apache                                             NONE   3&lt;br /&gt;
REVDAT   1  16-Nov-06     0                                             NONE   4&lt;br /&gt;
ATOM      1  O           0       3.779  -0.333   0.251  0.00  0.00           O+0&lt;br /&gt;
ATOM      2  C           0       2.568   0.160  -0.050  0.00  0.00           C+0&lt;br /&gt;
ATOM      3  C           0       1.326  -0.540   0.437  0.00  0.00           C+0&lt;br /&gt;
ATOM      4  C           0       0.089   0.222  -0.042  0.00  0.00           C+0&lt;br /&gt;
ATOM      5  C           0      -1.172  -0.489   0.453  0.00  0.00           C+0&lt;br /&gt;
ATOM      6  H           0      -1.124  -0.603   1.536  0.00  0.00           H+0&lt;br /&gt;
ATOM      7  N           0      -1.265  -1.814  -0.174  0.00  0.00           N+0&lt;br /&gt;
ATOM      8  C           0      -2.385   0.327   0.088  0.00  0.00           C+0&lt;br /&gt;
ATOM      9  O           0      -3.155  -0.075  -0.769  0.00  0.00           O-1&lt;br /&gt;
ATOM     10  O           0      -2.598   1.389   0.648  0.00  0.00           O+0&lt;br /&gt;
ATOM     11  O           0       2.473   1.167  -0.713  0.00  0.00           O+0&lt;br /&gt;
ATOM     12  H           0       4.576   0.116  -0.061  0.00  0.00           H+0&lt;br /&gt;
ATOM     13  H           0       1.302  -1.556   0.041  0.00  0.00           H+0&lt;br /&gt;
ATOM     14  H           0       1.332  -0.575   1.527  0.00  0.00           H+0&lt;br /&gt;
ATOM     15  H           0       0.112   1.238   0.354  0.00  0.00           H+0&lt;br /&gt;
ATOM     16  H           0       0.083   0.257  -1.131  0.00  0.00           H+0&lt;br /&gt;
ATOM     17  H           0      -1.307  -1.660  -1.171  0.00  0.00           H+0&lt;br /&gt;
ATOM     18  H           0      -0.392  -2.284   0.010  0.00  0.00           H+0&lt;br /&gt;
CONECT    1    2   12    0    0                                         NONE  23&lt;br /&gt;
CONECT    2    1    3   11    0                                         NONE  24&lt;br /&gt;
CONECT    3    2    4   13   14                                         NONE  25&lt;br /&gt;
CONECT    4    3    5   15   16                                         NONE  26&lt;br /&gt;
CONECT    5    4    6    7    8                                         NONE  27&lt;br /&gt;
CONECT    7    5   17   18    0                                         NONE  28&lt;br /&gt;
CONECT    8    5    9   10    0                                         NONE  29&lt;br /&gt;
CONECT    9    8    0    0    0                                         NONE  30&lt;br /&gt;
CONECT   10    8    0    0    0                                         NONE  31&lt;br /&gt;
CONECT   11    2    0    0    0                                         NONE  32&lt;br /&gt;
END                                                                     NONE  33&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;
&lt;br /&gt;
==References &amp;amp; Useful Links==&lt;br /&gt;
Image: http://www.germes-online.com/catalog/48/55/189/257161/monosodium_glutamate.html&lt;br /&gt;
&lt;br /&gt;
http://www.chemicalland21.com/lifescience/foco/MONOSODIUM%20GLUTAMATE.htm&lt;/div&gt;</summary>
		<author><name>Rw305</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It:MSG&amp;diff=5464</id>
		<title>It:MSG</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It:MSG&amp;diff=5464"/>
		<updated>2006-11-16T14:28:36Z</updated>

		<summary type="html">&lt;p&gt;Rw305: /* Abstract */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;==Abstract==&lt;br /&gt;
[[Image:msg.jpg]]&lt;br /&gt;
&#039;&#039;&#039;Monosodium Glutamate&#039;&#039;&#039; is more commonly known as &#039;&#039;&#039;MSG&#039;&#039;&#039; and has become the choice chemical for the enhancement of flavour in many foods. It was originally discovered in 1909 by the Ajinomoto Corporation in Japan.&lt;br /&gt;
&lt;br /&gt;
==The Basics==&lt;br /&gt;
{| class=&amp;quot;toccolours&amp;quot; border=&amp;quot;1&amp;quot; style=&amp;quot;float: right; clear: right; margin: 0 0 1em 1em; border-collapse: collapse;&amp;quot;&lt;br /&gt;
! {{chembox header}} | MSG &lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; width=&amp;quot;300&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image:msg.jpg]]&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | General&lt;br /&gt;
|-&lt;br /&gt;
| IUPAC nomenclature|Systematic name&lt;br /&gt;
|2-aminopentanedioic acid&lt;br /&gt;
|-&lt;br /&gt;
| Other names&lt;br /&gt;
|2-aminoglutaric acid, 1-aminopropane-1,&lt;br /&gt;
3-dicarboxylic acid&lt;br /&gt;
|-&lt;br /&gt;
| Chemical formula|Molecular formula]&lt;br /&gt;
|C&amp;lt;sub&amp;gt;5&amp;lt;/sub&amp;gt;H&amp;lt;sub&amp;gt;8&amp;lt;/sub&amp;gt;NNaO&amp;lt;sub&amp;gt;4&amp;lt;/sub&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
|-&lt;br /&gt;
| Molecular Weight&lt;br /&gt;
| 169.11&lt;br /&gt;
|-&lt;br /&gt;
| Appearance&lt;br /&gt;
| White Crystalline Solid&lt;br /&gt;
|-&lt;br /&gt;
| CAS registry number|CAS number&lt;br /&gt;
|142-47-2&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Properties&lt;br /&gt;
|-&lt;br /&gt;
| Melting point&lt;br /&gt;
| 232 °C (505 K)&lt;br /&gt;
|-&lt;br /&gt;
| Related compounds &lt;br /&gt;
| Glutamic Acid&lt;br /&gt;
|-&lt;br /&gt;
| Solubility in Water&lt;br /&gt;
| 100 mg/100ml&lt;br /&gt;
|-&lt;br /&gt;
| pH&lt;br /&gt;
| 7.0&lt;br /&gt;
|-&lt;br /&gt;
| {{chembox header}} | &amp;lt;small&amp;gt;Except where noted otherwise, data are given for&amp;lt;br /&amp;gt; materials in their [[standard state|standard state (at 25&amp;amp;nbsp;°C, 100&amp;amp;nbsp;kPa)]]&amp;lt;br /&amp;gt;[[wikipedia:Chemical infobox|Infobox disclaimer and references]]&amp;lt;/small&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
|}&lt;br /&gt;
MSG,is a sodium salt of the amino acid &#039;&#039;&#039;&#039;&#039;L-glutamic acid&#039;&#039;&#039;&#039;&#039;. It is practically odorless. It is produced by a bacterial fermentation process with starch or molasses as carbon sources and ammonium salts as nitrogen sources (Steffen process). MSG is not a direct taste enhancer but a complex flavour enhancer for gravies, meats, poultry, sauces, and in other combinations. It is also used to enhance the taste of tobacco and has been used medically to treat hepatic coma.&lt;br /&gt;
&lt;br /&gt;
===3D Representation===&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;green&amp;lt;/color&amp;gt;&lt;br /&gt;
&amp;lt;script&amp;gt;zoom 150; 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;&lt;br /&gt;
HEADER    NONAME 16-Nov-06                                              NONE   1&lt;br /&gt;
TITLE                                                                   NONE   2&lt;br /&gt;
AUTHOR    WWW daemon apache                                             NONE   3&lt;br /&gt;
REVDAT   1  16-Nov-06     0                                             NONE   4&lt;br /&gt;
ATOM      1  O           0       3.779  -0.333   0.251  0.00  0.00           O+0&lt;br /&gt;
ATOM      2  C           0       2.568   0.160  -0.050  0.00  0.00           C+0&lt;br /&gt;
ATOM      3  C           0       1.326  -0.540   0.437  0.00  0.00           C+0&lt;br /&gt;
ATOM      4  C           0       0.089   0.222  -0.042  0.00  0.00           C+0&lt;br /&gt;
ATOM      5  C           0      -1.172  -0.489   0.453  0.00  0.00           C+0&lt;br /&gt;
ATOM      6  H           0      -1.124  -0.603   1.536  0.00  0.00           H+0&lt;br /&gt;
ATOM      7  N           0      -1.265  -1.814  -0.174  0.00  0.00           N+0&lt;br /&gt;
ATOM      8  C           0      -2.385   0.327   0.088  0.00  0.00           C+0&lt;br /&gt;
ATOM      9  O           0      -3.155  -0.075  -0.769  0.00  0.00           O-1&lt;br /&gt;
ATOM     10  O           0      -2.598   1.389   0.648  0.00  0.00           O+0&lt;br /&gt;
ATOM     11  O           0       2.473   1.167  -0.713  0.00  0.00           O+0&lt;br /&gt;
ATOM     12  H           0       4.576   0.116  -0.061  0.00  0.00           H+0&lt;br /&gt;
ATOM     13  H           0       1.302  -1.556   0.041  0.00  0.00           H+0&lt;br /&gt;
ATOM     14  H           0       1.332  -0.575   1.527  0.00  0.00           H+0&lt;br /&gt;
ATOM     15  H           0       0.112   1.238   0.354  0.00  0.00           H+0&lt;br /&gt;
ATOM     16  H           0       0.083   0.257  -1.131  0.00  0.00           H+0&lt;br /&gt;
ATOM     17  H           0      -1.307  -1.660  -1.171  0.00  0.00           H+0&lt;br /&gt;
ATOM     18  H           0      -0.392  -2.284   0.010  0.00  0.00           H+0&lt;br /&gt;
CONECT    1    2   12    0    0                                         NONE  23&lt;br /&gt;
CONECT    2    1    3   11    0                                         NONE  24&lt;br /&gt;
CONECT    3    2    4   13   14                                         NONE  25&lt;br /&gt;
CONECT    4    3    5   15   16                                         NONE  26&lt;br /&gt;
CONECT    5    4    6    7    8                                         NONE  27&lt;br /&gt;
CONECT    7    5   17   18    0                                         NONE  28&lt;br /&gt;
CONECT    8    5    9   10    0                                         NONE  29&lt;br /&gt;
CONECT    9    8    0    0    0                                         NONE  30&lt;br /&gt;
CONECT   10    8    0    0    0                                         NONE  31&lt;br /&gt;
CONECT   11    2    0    0    0                                         NONE  32&lt;br /&gt;
END                                                                     NONE  33&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;
&lt;br /&gt;
==References &amp;amp; Useful Links==&lt;br /&gt;
Image: http://www.germes-online.com/catalog/48/55/189/257161/monosodium_glutamate.html&lt;br /&gt;
&lt;br /&gt;
http://www.chemicalland21.com/lifescience/foco/MONOSODIUM%20GLUTAMATE.htm&lt;/div&gt;</summary>
		<author><name>Rw305</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It:MSG&amp;diff=5463</id>
		<title>It:MSG</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It:MSG&amp;diff=5463"/>
		<updated>2006-11-16T14:26:24Z</updated>

		<summary type="html">&lt;p&gt;Rw305: /* 3D Representation */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;==Abstract==&lt;br /&gt;
&#039;&#039;&#039;Monosodium Glutamate&#039;&#039;&#039; is more commonly known as &#039;&#039;&#039;MSG&#039;&#039;&#039; and has become the choice chemical for the enhancement of flavour in many foods. It was originally discovered in 1909 by the Ajinomoto Corporation in Japan.&lt;br /&gt;
&lt;br /&gt;
==The Basics==&lt;br /&gt;
{| class=&amp;quot;toccolours&amp;quot; border=&amp;quot;1&amp;quot; style=&amp;quot;float: right; clear: right; margin: 0 0 1em 1em; border-collapse: collapse;&amp;quot;&lt;br /&gt;
! {{chembox header}} | MSG &lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; width=&amp;quot;300&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image:msg.jpg]]&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | General&lt;br /&gt;
|-&lt;br /&gt;
| IUPAC nomenclature|Systematic name&lt;br /&gt;
|2-aminopentanedioic acid&lt;br /&gt;
|-&lt;br /&gt;
| Other names&lt;br /&gt;
|2-aminoglutaric acid, 1-aminopropane-1,&lt;br /&gt;
3-dicarboxylic acid&lt;br /&gt;
|-&lt;br /&gt;
| Chemical formula|Molecular formula]&lt;br /&gt;
|C&amp;lt;sub&amp;gt;5&amp;lt;/sub&amp;gt;H&amp;lt;sub&amp;gt;8&amp;lt;/sub&amp;gt;NNaO&amp;lt;sub&amp;gt;4&amp;lt;/sub&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
|-&lt;br /&gt;
| Molecular Weight&lt;br /&gt;
| 169.11&lt;br /&gt;
|-&lt;br /&gt;
| Appearance&lt;br /&gt;
| White Crystalline Solid&lt;br /&gt;
|-&lt;br /&gt;
| CAS registry number|CAS number&lt;br /&gt;
|142-47-2&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Properties&lt;br /&gt;
|-&lt;br /&gt;
| Melting point&lt;br /&gt;
| 232 °C (505 K)&lt;br /&gt;
|-&lt;br /&gt;
| Related compounds &lt;br /&gt;
| Glutamic Acid&lt;br /&gt;
|-&lt;br /&gt;
| Solubility in Water&lt;br /&gt;
| 100 mg/100ml&lt;br /&gt;
|-&lt;br /&gt;
| pH&lt;br /&gt;
| 7.0&lt;br /&gt;
|-&lt;br /&gt;
| {{chembox header}} | &amp;lt;small&amp;gt;Except where noted otherwise, data are given for&amp;lt;br /&amp;gt; materials in their [[standard state|standard state (at 25&amp;amp;nbsp;°C, 100&amp;amp;nbsp;kPa)]]&amp;lt;br /&amp;gt;[[wikipedia:Chemical infobox|Infobox disclaimer and references]]&amp;lt;/small&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
|}&lt;br /&gt;
MSG,is a sodium salt of the amino acid &#039;&#039;&#039;&#039;&#039;L-glutamic acid&#039;&#039;&#039;&#039;&#039;. It is practically odorless. It is produced by a bacterial fermentation process with starch or molasses as carbon sources and ammonium salts as nitrogen sources (Steffen process). MSG is not a direct taste enhancer but a complex flavour enhancer for gravies, meats, poultry, sauces, and in other combinations. It is also used to enhance the taste of tobacco and has been used medically to treat hepatic coma.&lt;br /&gt;
&lt;br /&gt;
===3D Representation===&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;green&amp;lt;/color&amp;gt;&lt;br /&gt;
&amp;lt;script&amp;gt;zoom 150; 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;&lt;br /&gt;
HEADER    NONAME 16-Nov-06                                              NONE   1&lt;br /&gt;
TITLE                                                                   NONE   2&lt;br /&gt;
AUTHOR    WWW daemon apache                                             NONE   3&lt;br /&gt;
REVDAT   1  16-Nov-06     0                                             NONE   4&lt;br /&gt;
ATOM      1  O           0       3.779  -0.333   0.251  0.00  0.00           O+0&lt;br /&gt;
ATOM      2  C           0       2.568   0.160  -0.050  0.00  0.00           C+0&lt;br /&gt;
ATOM      3  C           0       1.326  -0.540   0.437  0.00  0.00           C+0&lt;br /&gt;
ATOM      4  C           0       0.089   0.222  -0.042  0.00  0.00           C+0&lt;br /&gt;
ATOM      5  C           0      -1.172  -0.489   0.453  0.00  0.00           C+0&lt;br /&gt;
ATOM      6  H           0      -1.124  -0.603   1.536  0.00  0.00           H+0&lt;br /&gt;
ATOM      7  N           0      -1.265  -1.814  -0.174  0.00  0.00           N+0&lt;br /&gt;
ATOM      8  C           0      -2.385   0.327   0.088  0.00  0.00           C+0&lt;br /&gt;
ATOM      9  O           0      -3.155  -0.075  -0.769  0.00  0.00           O-1&lt;br /&gt;
ATOM     10  O           0      -2.598   1.389   0.648  0.00  0.00           O+0&lt;br /&gt;
ATOM     11  O           0       2.473   1.167  -0.713  0.00  0.00           O+0&lt;br /&gt;
ATOM     12  H           0       4.576   0.116  -0.061  0.00  0.00           H+0&lt;br /&gt;
ATOM     13  H           0       1.302  -1.556   0.041  0.00  0.00           H+0&lt;br /&gt;
ATOM     14  H           0       1.332  -0.575   1.527  0.00  0.00           H+0&lt;br /&gt;
ATOM     15  H           0       0.112   1.238   0.354  0.00  0.00           H+0&lt;br /&gt;
ATOM     16  H           0       0.083   0.257  -1.131  0.00  0.00           H+0&lt;br /&gt;
ATOM     17  H           0      -1.307  -1.660  -1.171  0.00  0.00           H+0&lt;br /&gt;
ATOM     18  H           0      -0.392  -2.284   0.010  0.00  0.00           H+0&lt;br /&gt;
CONECT    1    2   12    0    0                                         NONE  23&lt;br /&gt;
CONECT    2    1    3   11    0                                         NONE  24&lt;br /&gt;
CONECT    3    2    4   13   14                                         NONE  25&lt;br /&gt;
CONECT    4    3    5   15   16                                         NONE  26&lt;br /&gt;
CONECT    5    4    6    7    8                                         NONE  27&lt;br /&gt;
CONECT    7    5   17   18    0                                         NONE  28&lt;br /&gt;
CONECT    8    5    9   10    0                                         NONE  29&lt;br /&gt;
CONECT    9    8    0    0    0                                         NONE  30&lt;br /&gt;
CONECT   10    8    0    0    0                                         NONE  31&lt;br /&gt;
CONECT   11    2    0    0    0                                         NONE  32&lt;br /&gt;
END                                                                     NONE  33&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;
&lt;br /&gt;
==References &amp;amp; Useful Links==&lt;br /&gt;
Image: http://www.germes-online.com/catalog/48/55/189/257161/monosodium_glutamate.html&lt;br /&gt;
&lt;br /&gt;
http://www.chemicalland21.com/lifescience/foco/MONOSODIUM%20GLUTAMATE.htm&lt;/div&gt;</summary>
		<author><name>Rw305</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It:MSG&amp;diff=5462</id>
		<title>It:MSG</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It:MSG&amp;diff=5462"/>
		<updated>2006-11-16T14:26:03Z</updated>

		<summary type="html">&lt;p&gt;Rw305: /* 3D Representation */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;==Abstract==&lt;br /&gt;
&#039;&#039;&#039;Monosodium Glutamate&#039;&#039;&#039; is more commonly known as &#039;&#039;&#039;MSG&#039;&#039;&#039; and has become the choice chemical for the enhancement of flavour in many foods. It was originally discovered in 1909 by the Ajinomoto Corporation in Japan.&lt;br /&gt;
&lt;br /&gt;
==The Basics==&lt;br /&gt;
{| class=&amp;quot;toccolours&amp;quot; border=&amp;quot;1&amp;quot; style=&amp;quot;float: right; clear: right; margin: 0 0 1em 1em; border-collapse: collapse;&amp;quot;&lt;br /&gt;
! {{chembox header}} | MSG &lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; width=&amp;quot;300&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image:msg.jpg]]&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | General&lt;br /&gt;
|-&lt;br /&gt;
| IUPAC nomenclature|Systematic name&lt;br /&gt;
|2-aminopentanedioic acid&lt;br /&gt;
|-&lt;br /&gt;
| Other names&lt;br /&gt;
|2-aminoglutaric acid, 1-aminopropane-1,&lt;br /&gt;
3-dicarboxylic acid&lt;br /&gt;
|-&lt;br /&gt;
| Chemical formula|Molecular formula]&lt;br /&gt;
|C&amp;lt;sub&amp;gt;5&amp;lt;/sub&amp;gt;H&amp;lt;sub&amp;gt;8&amp;lt;/sub&amp;gt;NNaO&amp;lt;sub&amp;gt;4&amp;lt;/sub&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
|-&lt;br /&gt;
| Molecular Weight&lt;br /&gt;
| 169.11&lt;br /&gt;
|-&lt;br /&gt;
| Appearance&lt;br /&gt;
| White Crystalline Solid&lt;br /&gt;
|-&lt;br /&gt;
| CAS registry number|CAS number&lt;br /&gt;
|142-47-2&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Properties&lt;br /&gt;
|-&lt;br /&gt;
| Melting point&lt;br /&gt;
| 232 °C (505 K)&lt;br /&gt;
|-&lt;br /&gt;
| Related compounds &lt;br /&gt;
| Glutamic Acid&lt;br /&gt;
|-&lt;br /&gt;
| Solubility in Water&lt;br /&gt;
| 100 mg/100ml&lt;br /&gt;
|-&lt;br /&gt;
| pH&lt;br /&gt;
| 7.0&lt;br /&gt;
|-&lt;br /&gt;
| {{chembox header}} | &amp;lt;small&amp;gt;Except where noted otherwise, data are given for&amp;lt;br /&amp;gt; materials in their [[standard state|standard state (at 25&amp;amp;nbsp;°C, 100&amp;amp;nbsp;kPa)]]&amp;lt;br /&amp;gt;[[wikipedia:Chemical infobox|Infobox disclaimer and references]]&amp;lt;/small&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
|}&lt;br /&gt;
MSG,is a sodium salt of the amino acid &#039;&#039;&#039;&#039;&#039;L-glutamic acid&#039;&#039;&#039;&#039;&#039;. It is practically odorless. It is produced by a bacterial fermentation process with starch or molasses as carbon sources and ammonium salts as nitrogen sources (Steffen process). MSG is not a direct taste enhancer but a complex flavour enhancer for gravies, meats, poultry, sauces, and in other combinations. It is also used to enhance the taste of tobacco and has been used medically to treat hepatic coma.&lt;br /&gt;
&lt;br /&gt;
===3D Representation===&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;lilac&amp;lt;/color&amp;gt;&lt;br /&gt;
&amp;lt;script&amp;gt;zoom 100; 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;&lt;br /&gt;
HEADER    NONAME 16-Nov-06                                              NONE   1&lt;br /&gt;
TITLE                                                                   NONE   2&lt;br /&gt;
AUTHOR    WWW daemon apache                                             NONE   3&lt;br /&gt;
REVDAT   1  16-Nov-06     0                                             NONE   4&lt;br /&gt;
ATOM      1  O           0       3.779  -0.333   0.251  0.00  0.00           O+0&lt;br /&gt;
ATOM      2  C           0       2.568   0.160  -0.050  0.00  0.00           C+0&lt;br /&gt;
ATOM      3  C           0       1.326  -0.540   0.437  0.00  0.00           C+0&lt;br /&gt;
ATOM      4  C           0       0.089   0.222  -0.042  0.00  0.00           C+0&lt;br /&gt;
ATOM      5  C           0      -1.172  -0.489   0.453  0.00  0.00           C+0&lt;br /&gt;
ATOM      6  H           0      -1.124  -0.603   1.536  0.00  0.00           H+0&lt;br /&gt;
ATOM      7  N           0      -1.265  -1.814  -0.174  0.00  0.00           N+0&lt;br /&gt;
ATOM      8  C           0      -2.385   0.327   0.088  0.00  0.00           C+0&lt;br /&gt;
ATOM      9  O           0      -3.155  -0.075  -0.769  0.00  0.00           O-1&lt;br /&gt;
ATOM     10  O           0      -2.598   1.389   0.648  0.00  0.00           O+0&lt;br /&gt;
ATOM     11  O           0       2.473   1.167  -0.713  0.00  0.00           O+0&lt;br /&gt;
ATOM     12  H           0       4.576   0.116  -0.061  0.00  0.00           H+0&lt;br /&gt;
ATOM     13  H           0       1.302  -1.556   0.041  0.00  0.00           H+0&lt;br /&gt;
ATOM     14  H           0       1.332  -0.575   1.527  0.00  0.00           H+0&lt;br /&gt;
ATOM     15  H           0       0.112   1.238   0.354  0.00  0.00           H+0&lt;br /&gt;
ATOM     16  H           0       0.083   0.257  -1.131  0.00  0.00           H+0&lt;br /&gt;
ATOM     17  H           0      -1.307  -1.660  -1.171  0.00  0.00           H+0&lt;br /&gt;
ATOM     18  H           0      -0.392  -2.284   0.010  0.00  0.00           H+0&lt;br /&gt;
CONECT    1    2   12    0    0                                         NONE  23&lt;br /&gt;
CONECT    2    1    3   11    0                                         NONE  24&lt;br /&gt;
CONECT    3    2    4   13   14                                         NONE  25&lt;br /&gt;
CONECT    4    3    5   15   16                                         NONE  26&lt;br /&gt;
CONECT    5    4    6    7    8                                         NONE  27&lt;br /&gt;
CONECT    7    5   17   18    0                                         NONE  28&lt;br /&gt;
CONECT    8    5    9   10    0                                         NONE  29&lt;br /&gt;
CONECT    9    8    0    0    0                                         NONE  30&lt;br /&gt;
CONECT   10    8    0    0    0                                         NONE  31&lt;br /&gt;
CONECT   11    2    0    0    0                                         NONE  32&lt;br /&gt;
END                                                                     NONE  33&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;
&lt;br /&gt;
==References &amp;amp; Useful Links==&lt;br /&gt;
Image: http://www.germes-online.com/catalog/48/55/189/257161/monosodium_glutamate.html&lt;br /&gt;
&lt;br /&gt;
http://www.chemicalland21.com/lifescience/foco/MONOSODIUM%20GLUTAMATE.htm&lt;/div&gt;</summary>
		<author><name>Rw305</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It:MSG&amp;diff=5461</id>
		<title>It:MSG</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It:MSG&amp;diff=5461"/>
		<updated>2006-11-16T14:25:43Z</updated>

		<summary type="html">&lt;p&gt;Rw305: /* 3D Representation */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;==Abstract==&lt;br /&gt;
&#039;&#039;&#039;Monosodium Glutamate&#039;&#039;&#039; is more commonly known as &#039;&#039;&#039;MSG&#039;&#039;&#039; and has become the choice chemical for the enhancement of flavour in many foods. It was originally discovered in 1909 by the Ajinomoto Corporation in Japan.&lt;br /&gt;
&lt;br /&gt;
==The Basics==&lt;br /&gt;
{| class=&amp;quot;toccolours&amp;quot; border=&amp;quot;1&amp;quot; style=&amp;quot;float: right; clear: right; margin: 0 0 1em 1em; border-collapse: collapse;&amp;quot;&lt;br /&gt;
! {{chembox header}} | MSG &lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; width=&amp;quot;300&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image:msg.jpg]]&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | General&lt;br /&gt;
|-&lt;br /&gt;
| IUPAC nomenclature|Systematic name&lt;br /&gt;
|2-aminopentanedioic acid&lt;br /&gt;
|-&lt;br /&gt;
| Other names&lt;br /&gt;
|2-aminoglutaric acid, 1-aminopropane-1,&lt;br /&gt;
3-dicarboxylic acid&lt;br /&gt;
|-&lt;br /&gt;
| Chemical formula|Molecular formula]&lt;br /&gt;
|C&amp;lt;sub&amp;gt;5&amp;lt;/sub&amp;gt;H&amp;lt;sub&amp;gt;8&amp;lt;/sub&amp;gt;NNaO&amp;lt;sub&amp;gt;4&amp;lt;/sub&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
|-&lt;br /&gt;
| Molecular Weight&lt;br /&gt;
| 169.11&lt;br /&gt;
|-&lt;br /&gt;
| Appearance&lt;br /&gt;
| White Crystalline Solid&lt;br /&gt;
|-&lt;br /&gt;
| CAS registry number|CAS number&lt;br /&gt;
|142-47-2&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Properties&lt;br /&gt;
|-&lt;br /&gt;
| Melting point&lt;br /&gt;
| 232 °C (505 K)&lt;br /&gt;
|-&lt;br /&gt;
| Related compounds &lt;br /&gt;
| Glutamic Acid&lt;br /&gt;
|-&lt;br /&gt;
| Solubility in Water&lt;br /&gt;
| 100 mg/100ml&lt;br /&gt;
|-&lt;br /&gt;
| pH&lt;br /&gt;
| 7.0&lt;br /&gt;
|-&lt;br /&gt;
| {{chembox header}} | &amp;lt;small&amp;gt;Except where noted otherwise, data are given for&amp;lt;br /&amp;gt; materials in their [[standard state|standard state (at 25&amp;amp;nbsp;°C, 100&amp;amp;nbsp;kPa)]]&amp;lt;br /&amp;gt;[[wikipedia:Chemical infobox|Infobox disclaimer and references]]&amp;lt;/small&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
|}&lt;br /&gt;
MSG,is a sodium salt of the amino acid &#039;&#039;&#039;&#039;&#039;L-glutamic acid&#039;&#039;&#039;&#039;&#039;. It is practically odorless. It is produced by a bacterial fermentation process with starch or molasses as carbon sources and ammonium salts as nitrogen sources (Steffen process). MSG is not a direct taste enhancer but a complex flavour enhancer for gravies, meats, poultry, sauces, and in other combinations. It is also used to enhance the taste of tobacco and has been used medically to treat hepatic coma.&lt;br /&gt;
&lt;br /&gt;
===3D Representation===&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;blue&amp;lt;/color&amp;gt;&lt;br /&gt;
&amp;lt;script&amp;gt;zoom 150; cpk on;frame 1; move 10 -20 10 0 0 0 0 0 3; delay 1;&amp;lt;/script&amp;gt;&lt;br /&gt;
&amp;lt;inlineContents&amp;gt;&lt;br /&gt;
HEADER    NONAME 16-Nov-06                                              NONE   1&lt;br /&gt;
TITLE                                                                   NONE   2&lt;br /&gt;
AUTHOR    WWW daemon apache                                             NONE   3&lt;br /&gt;
REVDAT   1  16-Nov-06     0                                             NONE   4&lt;br /&gt;
ATOM      1  O           0       3.779  -0.333   0.251  0.00  0.00           O+0&lt;br /&gt;
ATOM      2  C           0       2.568   0.160  -0.050  0.00  0.00           C+0&lt;br /&gt;
ATOM      3  C           0       1.326  -0.540   0.437  0.00  0.00           C+0&lt;br /&gt;
ATOM      4  C           0       0.089   0.222  -0.042  0.00  0.00           C+0&lt;br /&gt;
ATOM      5  C           0      -1.172  -0.489   0.453  0.00  0.00           C+0&lt;br /&gt;
ATOM      6  H           0      -1.124  -0.603   1.536  0.00  0.00           H+0&lt;br /&gt;
ATOM      7  N           0      -1.265  -1.814  -0.174  0.00  0.00           N+0&lt;br /&gt;
ATOM      8  C           0      -2.385   0.327   0.088  0.00  0.00           C+0&lt;br /&gt;
ATOM      9  O           0      -3.155  -0.075  -0.769  0.00  0.00           O-1&lt;br /&gt;
ATOM     10  O           0      -2.598   1.389   0.648  0.00  0.00           O+0&lt;br /&gt;
ATOM     11  O           0       2.473   1.167  -0.713  0.00  0.00           O+0&lt;br /&gt;
ATOM     12  H           0       4.576   0.116  -0.061  0.00  0.00           H+0&lt;br /&gt;
ATOM     13  H           0       1.302  -1.556   0.041  0.00  0.00           H+0&lt;br /&gt;
ATOM     14  H           0       1.332  -0.575   1.527  0.00  0.00           H+0&lt;br /&gt;
ATOM     15  H           0       0.112   1.238   0.354  0.00  0.00           H+0&lt;br /&gt;
ATOM     16  H           0       0.083   0.257  -1.131  0.00  0.00           H+0&lt;br /&gt;
ATOM     17  H           0      -1.307  -1.660  -1.171  0.00  0.00           H+0&lt;br /&gt;
ATOM     18  H           0      -0.392  -2.284   0.010  0.00  0.00           H+0&lt;br /&gt;
CONECT    1    2   12    0    0                                         NONE  23&lt;br /&gt;
CONECT    2    1    3   11    0                                         NONE  24&lt;br /&gt;
CONECT    3    2    4   13   14                                         NONE  25&lt;br /&gt;
CONECT    4    3    5   15   16                                         NONE  26&lt;br /&gt;
CONECT    5    4    6    7    8                                         NONE  27&lt;br /&gt;
CONECT    7    5   17   18    0                                         NONE  28&lt;br /&gt;
CONECT    8    5    9   10    0                                         NONE  29&lt;br /&gt;
CONECT    9    8    0    0    0                                         NONE  30&lt;br /&gt;
CONECT   10    8    0    0    0                                         NONE  31&lt;br /&gt;
CONECT   11    2    0    0    0                                         NONE  32&lt;br /&gt;
END                                                                     NONE  33&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;
&lt;br /&gt;
==References &amp;amp; Useful Links==&lt;br /&gt;
Image: http://www.germes-online.com/catalog/48/55/189/257161/monosodium_glutamate.html&lt;br /&gt;
&lt;br /&gt;
http://www.chemicalland21.com/lifescience/foco/MONOSODIUM%20GLUTAMATE.htm&lt;/div&gt;</summary>
		<author><name>Rw305</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It:MSG&amp;diff=5460</id>
		<title>It:MSG</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It:MSG&amp;diff=5460"/>
		<updated>2006-11-16T14:24:57Z</updated>

		<summary type="html">&lt;p&gt;Rw305: /* 3D Representation */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;==Abstract==&lt;br /&gt;
&#039;&#039;&#039;Monosodium Glutamate&#039;&#039;&#039; is more commonly known as &#039;&#039;&#039;MSG&#039;&#039;&#039; and has become the choice chemical for the enhancement of flavour in many foods. It was originally discovered in 1909 by the Ajinomoto Corporation in Japan.&lt;br /&gt;
&lt;br /&gt;
==The Basics==&lt;br /&gt;
{| class=&amp;quot;toccolours&amp;quot; border=&amp;quot;1&amp;quot; style=&amp;quot;float: right; clear: right; margin: 0 0 1em 1em; border-collapse: collapse;&amp;quot;&lt;br /&gt;
! {{chembox header}} | MSG &lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; width=&amp;quot;300&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image:msg.jpg]]&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | General&lt;br /&gt;
|-&lt;br /&gt;
| IUPAC nomenclature|Systematic name&lt;br /&gt;
|2-aminopentanedioic acid&lt;br /&gt;
|-&lt;br /&gt;
| Other names&lt;br /&gt;
|2-aminoglutaric acid, 1-aminopropane-1,&lt;br /&gt;
3-dicarboxylic acid&lt;br /&gt;
|-&lt;br /&gt;
| Chemical formula|Molecular formula]&lt;br /&gt;
|C&amp;lt;sub&amp;gt;5&amp;lt;/sub&amp;gt;H&amp;lt;sub&amp;gt;8&amp;lt;/sub&amp;gt;NNaO&amp;lt;sub&amp;gt;4&amp;lt;/sub&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
|-&lt;br /&gt;
| Molecular Weight&lt;br /&gt;
| 169.11&lt;br /&gt;
|-&lt;br /&gt;
| Appearance&lt;br /&gt;
| White Crystalline Solid&lt;br /&gt;
|-&lt;br /&gt;
| CAS registry number|CAS number&lt;br /&gt;
|142-47-2&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Properties&lt;br /&gt;
|-&lt;br /&gt;
| Melting point&lt;br /&gt;
| 232 °C (505 K)&lt;br /&gt;
|-&lt;br /&gt;
| Related compounds &lt;br /&gt;
| Glutamic Acid&lt;br /&gt;
|-&lt;br /&gt;
| Solubility in Water&lt;br /&gt;
| 100 mg/100ml&lt;br /&gt;
|-&lt;br /&gt;
| pH&lt;br /&gt;
| 7.0&lt;br /&gt;
|-&lt;br /&gt;
| {{chembox header}} | &amp;lt;small&amp;gt;Except where noted otherwise, data are given for&amp;lt;br /&amp;gt; materials in their [[standard state|standard state (at 25&amp;amp;nbsp;°C, 100&amp;amp;nbsp;kPa)]]&amp;lt;br /&amp;gt;[[wikipedia:Chemical infobox|Infobox disclaimer and references]]&amp;lt;/small&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
|}&lt;br /&gt;
MSG,is a sodium salt of the amino acid &#039;&#039;&#039;&#039;&#039;L-glutamic acid&#039;&#039;&#039;&#039;&#039;. It is practically odorless. It is produced by a bacterial fermentation process with starch or molasses as carbon sources and ammonium salts as nitrogen sources (Steffen process). MSG is not a direct taste enhancer but a complex flavour enhancer for gravies, meats, poultry, sauces, and in other combinations. It is also used to enhance the taste of tobacco and has been used medically to treat hepatic coma.&lt;br /&gt;
&lt;br /&gt;
===3D Representation===&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;light blue&amp;lt;/color&amp;gt;&lt;br /&gt;
&amp;lt;script&amp;gt;zoom 150; cpk off;frame 50; 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;&lt;br /&gt;
HEADER    NONAME 16-Nov-06                                              NONE   1&lt;br /&gt;
TITLE                                                                   NONE   2&lt;br /&gt;
AUTHOR    WWW daemon apache                                             NONE   3&lt;br /&gt;
REVDAT   1  16-Nov-06     0                                             NONE   4&lt;br /&gt;
ATOM      1  O           0       3.779  -0.333   0.251  0.00  0.00           O+0&lt;br /&gt;
ATOM      2  C           0       2.568   0.160  -0.050  0.00  0.00           C+0&lt;br /&gt;
ATOM      3  C           0       1.326  -0.540   0.437  0.00  0.00           C+0&lt;br /&gt;
ATOM      4  C           0       0.089   0.222  -0.042  0.00  0.00           C+0&lt;br /&gt;
ATOM      5  C           0      -1.172  -0.489   0.453  0.00  0.00           C+0&lt;br /&gt;
ATOM      6  H           0      -1.124  -0.603   1.536  0.00  0.00           H+0&lt;br /&gt;
ATOM      7  N           0      -1.265  -1.814  -0.174  0.00  0.00           N+0&lt;br /&gt;
ATOM      8  C           0      -2.385   0.327   0.088  0.00  0.00           C+0&lt;br /&gt;
ATOM      9  O           0      -3.155  -0.075  -0.769  0.00  0.00           O-1&lt;br /&gt;
ATOM     10  O           0      -2.598   1.389   0.648  0.00  0.00           O+0&lt;br /&gt;
ATOM     11  O           0       2.473   1.167  -0.713  0.00  0.00           O+0&lt;br /&gt;
ATOM     12  H           0       4.576   0.116  -0.061  0.00  0.00           H+0&lt;br /&gt;
ATOM     13  H           0       1.302  -1.556   0.041  0.00  0.00           H+0&lt;br /&gt;
ATOM     14  H           0       1.332  -0.575   1.527  0.00  0.00           H+0&lt;br /&gt;
ATOM     15  H           0       0.112   1.238   0.354  0.00  0.00           H+0&lt;br /&gt;
ATOM     16  H           0       0.083   0.257  -1.131  0.00  0.00           H+0&lt;br /&gt;
ATOM     17  H           0      -1.307  -1.660  -1.171  0.00  0.00           H+0&lt;br /&gt;
ATOM     18  H           0      -0.392  -2.284   0.010  0.00  0.00           H+0&lt;br /&gt;
CONECT    1    2   12    0    0                                         NONE  23&lt;br /&gt;
CONECT    2    1    3   11    0                                         NONE  24&lt;br /&gt;
CONECT    3    2    4   13   14                                         NONE  25&lt;br /&gt;
CONECT    4    3    5   15   16                                         NONE  26&lt;br /&gt;
CONECT    5    4    6    7    8                                         NONE  27&lt;br /&gt;
CONECT    7    5   17   18    0                                         NONE  28&lt;br /&gt;
CONECT    8    5    9   10    0                                         NONE  29&lt;br /&gt;
CONECT    9    8    0    0    0                                         NONE  30&lt;br /&gt;
CONECT   10    8    0    0    0                                         NONE  31&lt;br /&gt;
CONECT   11    2    0    0    0                                         NONE  32&lt;br /&gt;
END                                                                     NONE  33&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;
&lt;br /&gt;
==References &amp;amp; Useful Links==&lt;br /&gt;
Image: http://www.germes-online.com/catalog/48/55/189/257161/monosodium_glutamate.html&lt;br /&gt;
&lt;br /&gt;
http://www.chemicalland21.com/lifescience/foco/MONOSODIUM%20GLUTAMATE.htm&lt;/div&gt;</summary>
		<author><name>Rw305</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It:MSG&amp;diff=5459</id>
		<title>It:MSG</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It:MSG&amp;diff=5459"/>
		<updated>2006-11-16T14:18:05Z</updated>

		<summary type="html">&lt;p&gt;Rw305: /* 3D Representation */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;==Abstract==&lt;br /&gt;
&#039;&#039;&#039;Monosodium Glutamate&#039;&#039;&#039; is more commonly known as &#039;&#039;&#039;MSG&#039;&#039;&#039; and has become the choice chemical for the enhancement of flavour in many foods. It was originally discovered in 1909 by the Ajinomoto Corporation in Japan.&lt;br /&gt;
&lt;br /&gt;
==The Basics==&lt;br /&gt;
{| class=&amp;quot;toccolours&amp;quot; border=&amp;quot;1&amp;quot; style=&amp;quot;float: right; clear: right; margin: 0 0 1em 1em; border-collapse: collapse;&amp;quot;&lt;br /&gt;
! {{chembox header}} | MSG &lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; width=&amp;quot;300&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image:msg.jpg]]&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | General&lt;br /&gt;
|-&lt;br /&gt;
| IUPAC nomenclature|Systematic name&lt;br /&gt;
|2-aminopentanedioic acid&lt;br /&gt;
|-&lt;br /&gt;
| Other names&lt;br /&gt;
|2-aminoglutaric acid, 1-aminopropane-1,&lt;br /&gt;
3-dicarboxylic acid&lt;br /&gt;
|-&lt;br /&gt;
| Chemical formula|Molecular formula]&lt;br /&gt;
|C&amp;lt;sub&amp;gt;5&amp;lt;/sub&amp;gt;H&amp;lt;sub&amp;gt;8&amp;lt;/sub&amp;gt;NNaO&amp;lt;sub&amp;gt;4&amp;lt;/sub&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
|-&lt;br /&gt;
| Molecular Weight&lt;br /&gt;
| 169.11&lt;br /&gt;
|-&lt;br /&gt;
| Appearance&lt;br /&gt;
| White Crystalline Solid&lt;br /&gt;
|-&lt;br /&gt;
| CAS registry number|CAS number&lt;br /&gt;
|142-47-2&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Properties&lt;br /&gt;
|-&lt;br /&gt;
| Melting point&lt;br /&gt;
| 232 °C (505 K)&lt;br /&gt;
|-&lt;br /&gt;
| Related compounds &lt;br /&gt;
| Glutamic Acid&lt;br /&gt;
|-&lt;br /&gt;
| Solubility in Water&lt;br /&gt;
| 100 mg/100ml&lt;br /&gt;
|-&lt;br /&gt;
| pH&lt;br /&gt;
| 7.0&lt;br /&gt;
|-&lt;br /&gt;
| {{chembox header}} | &amp;lt;small&amp;gt;Except where noted otherwise, data are given for&amp;lt;br /&amp;gt; materials in their [[standard state|standard state (at 25&amp;amp;nbsp;°C, 100&amp;amp;nbsp;kPa)]]&amp;lt;br /&amp;gt;[[wikipedia:Chemical infobox|Infobox disclaimer and references]]&amp;lt;/small&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
|}&lt;br /&gt;
MSG,is a sodium salt of the amino acid &#039;&#039;&#039;&#039;&#039;L-glutamic acid&#039;&#039;&#039;&#039;&#039;. It is practically odorless. It is produced by a bacterial fermentation process with starch or molasses as carbon sources and ammonium salts as nitrogen sources (Steffen process). MSG is not a direct taste enhancer but a complex flavour enhancer for gravies, meats, poultry, sauces, and in other combinations. It is also used to enhance the taste of tobacco and has been used medically to treat hepatic coma.&lt;br /&gt;
&lt;br /&gt;
===3D Representation===&lt;br /&gt;
&lt;br /&gt;
==References &amp;amp; Useful Links==&lt;br /&gt;
Image: http://www.germes-online.com/catalog/48/55/189/257161/monosodium_glutamate.html&lt;br /&gt;
&lt;br /&gt;
http://www.chemicalland21.com/lifescience/foco/MONOSODIUM%20GLUTAMATE.htm&lt;/div&gt;</summary>
		<author><name>Rw305</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It:MSG&amp;diff=5458</id>
		<title>It:MSG</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It:MSG&amp;diff=5458"/>
		<updated>2006-11-16T14:17:51Z</updated>

		<summary type="html">&lt;p&gt;Rw305: /* 3D Representation */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;==Abstract==&lt;br /&gt;
&#039;&#039;&#039;Monosodium Glutamate&#039;&#039;&#039; is more commonly known as &#039;&#039;&#039;MSG&#039;&#039;&#039; and has become the choice chemical for the enhancement of flavour in many foods. It was originally discovered in 1909 by the Ajinomoto Corporation in Japan.&lt;br /&gt;
&lt;br /&gt;
==The Basics==&lt;br /&gt;
{| class=&amp;quot;toccolours&amp;quot; border=&amp;quot;1&amp;quot; style=&amp;quot;float: right; clear: right; margin: 0 0 1em 1em; border-collapse: collapse;&amp;quot;&lt;br /&gt;
! {{chembox header}} | MSG &lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; width=&amp;quot;300&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image:msg.jpg]]&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | General&lt;br /&gt;
|-&lt;br /&gt;
| IUPAC nomenclature|Systematic name&lt;br /&gt;
|2-aminopentanedioic acid&lt;br /&gt;
|-&lt;br /&gt;
| Other names&lt;br /&gt;
|2-aminoglutaric acid, 1-aminopropane-1,&lt;br /&gt;
3-dicarboxylic acid&lt;br /&gt;
|-&lt;br /&gt;
| Chemical formula|Molecular formula]&lt;br /&gt;
|C&amp;lt;sub&amp;gt;5&amp;lt;/sub&amp;gt;H&amp;lt;sub&amp;gt;8&amp;lt;/sub&amp;gt;NNaO&amp;lt;sub&amp;gt;4&amp;lt;/sub&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
|-&lt;br /&gt;
| Molecular Weight&lt;br /&gt;
| 169.11&lt;br /&gt;
|-&lt;br /&gt;
| Appearance&lt;br /&gt;
| White Crystalline Solid&lt;br /&gt;
|-&lt;br /&gt;
| CAS registry number|CAS number&lt;br /&gt;
|142-47-2&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Properties&lt;br /&gt;
|-&lt;br /&gt;
| Melting point&lt;br /&gt;
| 232 °C (505 K)&lt;br /&gt;
|-&lt;br /&gt;
| Related compounds &lt;br /&gt;
| Glutamic Acid&lt;br /&gt;
|-&lt;br /&gt;
| Solubility in Water&lt;br /&gt;
| 100 mg/100ml&lt;br /&gt;
|-&lt;br /&gt;
| pH&lt;br /&gt;
| 7.0&lt;br /&gt;
|-&lt;br /&gt;
| {{chembox header}} | &amp;lt;small&amp;gt;Except where noted otherwise, data are given for&amp;lt;br /&amp;gt; materials in their [[standard state|standard state (at 25&amp;amp;nbsp;°C, 100&amp;amp;nbsp;kPa)]]&amp;lt;br /&amp;gt;[[wikipedia:Chemical infobox|Infobox disclaimer and references]]&amp;lt;/small&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
|}&lt;br /&gt;
MSG,is a sodium salt of the amino acid &#039;&#039;&#039;&#039;&#039;L-glutamic acid&#039;&#039;&#039;&#039;&#039;. It is practically odorless. It is produced by a bacterial fermentation process with starch or molasses as carbon sources and ammonium salts as nitrogen sources (Steffen process). MSG is not a direct taste enhancer but a complex flavour enhancer for gravies, meats, poultry, sauces, and in other combinations. It is also used to enhance the taste of tobacco and has been used medically to treat hepatic coma.&lt;br /&gt;
&lt;br /&gt;
===3D Representation===&lt;br /&gt;
&amp;lt;jmol&amp;gt;&lt;br /&gt;
&amp;lt;jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;size&amp;gt;400&amp;lt;/size&amp;gt;&lt;br /&gt;
&amp;lt;color&amp;gt;black&amp;lt;/color&amp;gt;&lt;br /&gt;
&amp;lt;script&amp;gt;zoom 80; cpk on;frame 2; move 10 -20 10 0 0 0 0 0 3; delay 1;&amp;lt;/script&amp;gt;&lt;br /&gt;
  18 17  0        0              1 V2000&lt;br /&gt;
    3.7760   -0.3320    0.2480 O   0  0  0  0  0  0  0  0  0  0  0  0&lt;br /&gt;
    2.5680    0.1600   -0.0480 C   0  0  0  0  0  0  0  0  0  0  0  0&lt;br /&gt;
    1.3240   -0.5400    0.4360 C   0  0  0  0  0  0  0  0  0  0  0  0&lt;br /&gt;
    0.0880    0.2200   -0.0400 C   0  0  0  0  0  0  0  0  0  0  0  0&lt;br /&gt;
   -1.1720   -0.4880    0.4520 C   0  0  0  0  0  0  0  0  0  0  0  0&lt;br /&gt;
   -1.1240   -0.6000    1.5360 H   0  0  0  0  0  0  0  0  0  0  0  0&lt;br /&gt;
   -1.2640   -1.8120   -0.1720 N   0  0  0  0  0  0  0  0  0  0  0  0&lt;br /&gt;
   -2.3840    0.3240    0.0880 C   0  0  0  0  0  0  0  0  0  0  0  0&lt;br /&gt;
   -3.1520   -0.0720   -0.7680 O   0  0  0  0  0  0  0  0  0  0  0  0&lt;br /&gt;
   -2.5960    1.3880    0.6480 O   0  0  0  0  0  0  0  0  0  0  0  0&lt;br /&gt;
    2.4720    1.1640   -0.7120 O   0  0  0  0  0  0  0  0  0  0  0  0&lt;br /&gt;
    4.5760    0.1160   -0.0600 H   0  0  0  0  0  0  0  0  0  0  0  0&lt;br /&gt;
    1.3000   -1.5560    0.0400 H   0  0  0  0  0  0  0  0  0  0  0  0&lt;br /&gt;
    1.3320   -0.5720    1.5240 H   0  0  0  0  0  0  0  0  0  0  0  0&lt;br /&gt;
    0.1120    1.2360    0.3520 H   0  0  0  0  0  0  0  0  0  0  0  0&lt;br /&gt;
    0.0800    0.2560   -1.1280 H   0  0  0  0  0  0  0  0  0  0  0  0&lt;br /&gt;
   -1.3040   -1.6600   -1.1680 H   0  0  0  0  0  0  0  0  0  0  0  0&lt;br /&gt;
   -0.3920   -2.2840    0.0080 H   0  0  0  0  0  0  0  0  0  0  0  0&lt;br /&gt;
  8 10  1  0&lt;br /&gt;
  8  9  1  0&lt;br /&gt;
  7 18  1  0&lt;br /&gt;
  7 17  1  0&lt;br /&gt;
  5  8  1  0&lt;br /&gt;
  5  7  1  0&lt;br /&gt;
  5  6  1  0&lt;br /&gt;
  4 16  1  0&lt;br /&gt;
  4 15  1  0&lt;br /&gt;
  4  5  1  0&lt;br /&gt;
  3 14  1  0&lt;br /&gt;
  3 13  1  0&lt;br /&gt;
  3  4  1  0&lt;br /&gt;
  2 11  1  0&lt;br /&gt;
  2  3  1  0&lt;br /&gt;
  1 12  1  0&lt;br /&gt;
  1  2  1  0&lt;br /&gt;
M  END&amp;lt;/inlineContents&amp;gt;&lt;br /&gt;
&amp;lt;/jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;/jmol&amp;gt;&lt;br /&gt;
&lt;br /&gt;
==References &amp;amp; Useful Links==&lt;br /&gt;
Image: http://www.germes-online.com/catalog/48/55/189/257161/monosodium_glutamate.html&lt;br /&gt;
&lt;br /&gt;
http://www.chemicalland21.com/lifescience/foco/MONOSODIUM%20GLUTAMATE.htm&lt;/div&gt;</summary>
		<author><name>Rw305</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It:MSG&amp;diff=5457</id>
		<title>It:MSG</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It:MSG&amp;diff=5457"/>
		<updated>2006-11-16T14:14:14Z</updated>

		<summary type="html">&lt;p&gt;Rw305: /* The Basics */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;==Abstract==&lt;br /&gt;
&#039;&#039;&#039;Monosodium Glutamate&#039;&#039;&#039; is more commonly known as &#039;&#039;&#039;MSG&#039;&#039;&#039; and has become the choice chemical for the enhancement of flavour in many foods. It was originally discovered in 1909 by the Ajinomoto Corporation in Japan.&lt;br /&gt;
&lt;br /&gt;
==The Basics==&lt;br /&gt;
{| class=&amp;quot;toccolours&amp;quot; border=&amp;quot;1&amp;quot; style=&amp;quot;float: right; clear: right; margin: 0 0 1em 1em; border-collapse: collapse;&amp;quot;&lt;br /&gt;
! {{chembox header}} | MSG &lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; width=&amp;quot;300&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image:msg.jpg]]&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | General&lt;br /&gt;
|-&lt;br /&gt;
| IUPAC nomenclature|Systematic name&lt;br /&gt;
|2-aminopentanedioic acid&lt;br /&gt;
|-&lt;br /&gt;
| Other names&lt;br /&gt;
|2-aminoglutaric acid, 1-aminopropane-1,&lt;br /&gt;
3-dicarboxylic acid&lt;br /&gt;
|-&lt;br /&gt;
| Chemical formula|Molecular formula]&lt;br /&gt;
|C&amp;lt;sub&amp;gt;5&amp;lt;/sub&amp;gt;H&amp;lt;sub&amp;gt;8&amp;lt;/sub&amp;gt;NNaO&amp;lt;sub&amp;gt;4&amp;lt;/sub&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
|-&lt;br /&gt;
| Molecular Weight&lt;br /&gt;
| 169.11&lt;br /&gt;
|-&lt;br /&gt;
| Appearance&lt;br /&gt;
| White Crystalline Solid&lt;br /&gt;
|-&lt;br /&gt;
| CAS registry number|CAS number&lt;br /&gt;
|142-47-2&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Properties&lt;br /&gt;
|-&lt;br /&gt;
| Melting point&lt;br /&gt;
| 232 °C (505 K)&lt;br /&gt;
|-&lt;br /&gt;
| Related compounds &lt;br /&gt;
| Glutamic Acid&lt;br /&gt;
|-&lt;br /&gt;
| Solubility in Water&lt;br /&gt;
| 100 mg/100ml&lt;br /&gt;
|-&lt;br /&gt;
| pH&lt;br /&gt;
| 7.0&lt;br /&gt;
|-&lt;br /&gt;
| {{chembox header}} | &amp;lt;small&amp;gt;Except where noted otherwise, data are given for&amp;lt;br /&amp;gt; materials in their [[standard state|standard state (at 25&amp;amp;nbsp;°C, 100&amp;amp;nbsp;kPa)]]&amp;lt;br /&amp;gt;[[wikipedia:Chemical infobox|Infobox disclaimer and references]]&amp;lt;/small&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
|}&lt;br /&gt;
MSG,is a sodium salt of the amino acid &#039;&#039;&#039;&#039;&#039;L-glutamic acid&#039;&#039;&#039;&#039;&#039;. It is practically odorless. It is produced by a bacterial fermentation process with starch or molasses as carbon sources and ammonium salts as nitrogen sources (Steffen process). MSG is not a direct taste enhancer but a complex flavour enhancer for gravies, meats, poultry, sauces, and in other combinations. It is also used to enhance the taste of tobacco and has been used medically to treat hepatic coma.&lt;br /&gt;
&lt;br /&gt;
===3D Representation===&lt;br /&gt;
&amp;lt;jmol&amp;gt;&lt;br /&gt;
&amp;lt;jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;size&amp;gt;400&amp;lt;/size&amp;gt;&lt;br /&gt;
&amp;lt;color&amp;gt;purple&amp;lt;/color&amp;gt;&lt;br /&gt;
&amp;lt;script&amp;gt;zoom 80; 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;msg.mol&lt;br /&gt;
 19 17  0        0              1 V2000&lt;br /&gt;
    1.3880   -2.0960   -0.6080 O   0  0  0  0  0  0  0  0  0  0  0  0&lt;br /&gt;
    0.4160   -1.4120    0.0120 C   0  0  0  0  0  0  0  0  0  0  0  0&lt;br /&gt;
   -0.8240   -1.0080   -0.7360 C   0  0  0  0  0  0  0  0  0  0  0  0&lt;br /&gt;
   -1.7600   -0.2400    0.1960 C   0  0  0  0  0  0  0  0  0  0  0  0&lt;br /&gt;
   -3.0200    0.1680   -0.5640 C   0  0  0  0  0  0  0  0  0  0  0  0&lt;br /&gt;
   -3.4760   -0.7120   -1.0120 H   0  0  0  0  0  0  0  0  0  0  0  0&lt;br /&gt;
   -2.6640    1.1200   -1.6240 N   0  0  0  0  0  0  0  0  0  0  0  0&lt;br /&gt;
   -3.9960    0.8120    0.3800 C   0  0  0  0  0  0  0  0  0  0  0  0&lt;br /&gt;
   -4.2200    2.0080    0.3040 O   0  0  0  0  0  0  0  0  0  0  0  0&lt;br /&gt;
   -4.5600    0.1400    1.2280 O   0  0  0  0  0  0  0  0  0  0  0  0&lt;br /&gt;
    0.5400   -1.1160    1.1800 O   0  0  0  0  0  0  0  0  0  0  0  0&lt;br /&gt;
   11.6560    1.0640    0.1400 Na  0  0  0  0  0  0  0  0  0  0  0  0&lt;br /&gt;
    2.1840   -2.3560   -0.1240 H   0  0  0  0  0  0  0  0  0  0  0  0&lt;br /&gt;
   -0.5480   -0.3680   -1.5760 H   0  0  0  0  0  0  0  0  0  0  0  0&lt;br /&gt;
   -1.3280   -1.9000   -1.1080 H   0  0  0  0  0  0  0  0  0  0  0  0&lt;br /&gt;
   -2.0360   -0.8760    1.0360 H   0  0  0  0  0  0  0  0  0  0  0  0&lt;br /&gt;
   -1.2520    0.6480    0.5680 H   0  0  0  0  0  0  0  0  0  0  0  0&lt;br /&gt;
   -2.2440    1.9160   -1.1680 H   0  0  0  0  0  0  0  0  0  0  0  0&lt;br /&gt;
   -1.9360    0.6840   -2.1720 H   0  0  0  0  0  0  0  0  0  0  0  0&lt;br /&gt;
 19  7  1  0&lt;br /&gt;
 18  7  1  0&lt;br /&gt;
 17  4  1  0&lt;br /&gt;
 16  4  1  0&lt;br /&gt;
 15  3  1  0&lt;br /&gt;
 14  3  1  0&lt;br /&gt;
 13  1  1  0&lt;br /&gt;
 11  2  1  0&lt;br /&gt;
 10  8  1  0&lt;br /&gt;
  9  8  1  0&lt;br /&gt;
  8  5  1  0&lt;br /&gt;
  7  5  1  0&lt;br /&gt;
  6  5  1  0&lt;br /&gt;
  5  4  1  0&lt;br /&gt;
  4  3  1  0&lt;br /&gt;
  3  2  1  0&lt;br /&gt;
  2  1  1  0&lt;br /&gt;
M  END&amp;lt;/inlineContents&amp;gt;&lt;br /&gt;
&amp;lt;/jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;/jmol&amp;gt;&lt;br /&gt;
&lt;br /&gt;
==References &amp;amp; Useful Links==&lt;br /&gt;
Image: http://www.germes-online.com/catalog/48/55/189/257161/monosodium_glutamate.html&lt;br /&gt;
&lt;br /&gt;
http://www.chemicalland21.com/lifescience/foco/MONOSODIUM%20GLUTAMATE.htm&lt;/div&gt;</summary>
		<author><name>Rw305</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It:MSG&amp;diff=5456</id>
		<title>It:MSG</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It:MSG&amp;diff=5456"/>
		<updated>2006-11-16T14:05:42Z</updated>

		<summary type="html">&lt;p&gt;Rw305: /* References &amp;amp; Useful Links */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;==Abstract==&lt;br /&gt;
&#039;&#039;&#039;Monosodium Glutamate&#039;&#039;&#039; is more commonly known as &#039;&#039;&#039;MSG&#039;&#039;&#039; and has become the choice chemical for the enhancement of flavour in many foods. It was originally discovered in 1909 by the Ajinomoto Corporation in Japan.&lt;br /&gt;
&lt;br /&gt;
==The Basics==&lt;br /&gt;
{| class=&amp;quot;toccolours&amp;quot; border=&amp;quot;1&amp;quot; style=&amp;quot;float: right; clear: right; margin: 0 0 1em 1em; border-collapse: collapse;&amp;quot;&lt;br /&gt;
! {{chembox header}} | MSG &lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; width=&amp;quot;300&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image:msg.jpg]]&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | General&lt;br /&gt;
|-&lt;br /&gt;
| IUPAC nomenclature|Systematic name&lt;br /&gt;
|2-aminopentanedioic acid&lt;br /&gt;
|-&lt;br /&gt;
| Other names&lt;br /&gt;
|2-aminoglutaric acid, 1-aminopropane-1,&lt;br /&gt;
3-dicarboxylic acid&lt;br /&gt;
|-&lt;br /&gt;
| Chemical formula|Molecular formula]&lt;br /&gt;
|C&amp;lt;sub&amp;gt;5&amp;lt;/sub&amp;gt;H&amp;lt;sub&amp;gt;8&amp;lt;/sub&amp;gt;NNaO&amp;lt;sub&amp;gt;4&amp;lt;/sub&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
|-&lt;br /&gt;
| Molecular Weight&lt;br /&gt;
| 169.11&lt;br /&gt;
|-&lt;br /&gt;
| Appearance&lt;br /&gt;
| White Crystalline Solid&lt;br /&gt;
|-&lt;br /&gt;
| CAS registry number|CAS number&lt;br /&gt;
|142-47-2&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Properties&lt;br /&gt;
|-&lt;br /&gt;
| Melting point&lt;br /&gt;
| 232 °C (505 K)&lt;br /&gt;
|-&lt;br /&gt;
| Related compounds &lt;br /&gt;
| Glutamic Acid&lt;br /&gt;
|-&lt;br /&gt;
| Solubility in Water&lt;br /&gt;
| 100 mg/100ml&lt;br /&gt;
|-&lt;br /&gt;
| pH&lt;br /&gt;
| 7.0&lt;br /&gt;
|-&lt;br /&gt;
| {{chembox header}} | &amp;lt;small&amp;gt;Except where noted otherwise, data are given for&amp;lt;br /&amp;gt; materials in their [[standard state|standard state (at 25&amp;amp;nbsp;°C, 100&amp;amp;nbsp;kPa)]]&amp;lt;br /&amp;gt;[[wikipedia:Chemical infobox|Infobox disclaimer and references]]&amp;lt;/small&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
|}&lt;br /&gt;
MSG,is a sodium salt of the amino acid &#039;&#039;&#039;&#039;&#039;L-glutamic acid&#039;&#039;&#039;&#039;&#039;. It is practically odorless. It is produced by a bacterial fermentation process with starch or molasses as carbon sources and ammonium salts as nitrogen sources (Steffen process). MSG is not a direct taste enhancer but a complex flavour enhancer for gravies, meats, poultry, sauces, and in other combinations. It is also used to enhance the taste of tobacco and has been used medically to treat hepatic coma.&lt;br /&gt;
&lt;br /&gt;
==References &amp;amp; Useful Links==&lt;br /&gt;
Image: http://www.germes-online.com/catalog/48/55/189/257161/monosodium_glutamate.html&lt;br /&gt;
&lt;br /&gt;
http://www.chemicalland21.com/lifescience/foco/MONOSODIUM%20GLUTAMATE.htm&lt;/div&gt;</summary>
		<author><name>Rw305</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It:MSG&amp;diff=5455</id>
		<title>It:MSG</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It:MSG&amp;diff=5455"/>
		<updated>2006-11-16T14:05:19Z</updated>

		<summary type="html">&lt;p&gt;Rw305: /* The Basics */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;==Abstract==&lt;br /&gt;
&#039;&#039;&#039;Monosodium Glutamate&#039;&#039;&#039; is more commonly known as &#039;&#039;&#039;MSG&#039;&#039;&#039; and has become the choice chemical for the enhancement of flavour in many foods. It was originally discovered in 1909 by the Ajinomoto Corporation in Japan.&lt;br /&gt;
&lt;br /&gt;
==The Basics==&lt;br /&gt;
{| class=&amp;quot;toccolours&amp;quot; border=&amp;quot;1&amp;quot; style=&amp;quot;float: right; clear: right; margin: 0 0 1em 1em; border-collapse: collapse;&amp;quot;&lt;br /&gt;
! {{chembox header}} | MSG &lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; width=&amp;quot;300&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image:msg.jpg]]&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | General&lt;br /&gt;
|-&lt;br /&gt;
| IUPAC nomenclature|Systematic name&lt;br /&gt;
|2-aminopentanedioic acid&lt;br /&gt;
|-&lt;br /&gt;
| Other names&lt;br /&gt;
|2-aminoglutaric acid, 1-aminopropane-1,&lt;br /&gt;
3-dicarboxylic acid&lt;br /&gt;
|-&lt;br /&gt;
| Chemical formula|Molecular formula]&lt;br /&gt;
|C&amp;lt;sub&amp;gt;5&amp;lt;/sub&amp;gt;H&amp;lt;sub&amp;gt;8&amp;lt;/sub&amp;gt;NNaO&amp;lt;sub&amp;gt;4&amp;lt;/sub&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
|-&lt;br /&gt;
| Molecular Weight&lt;br /&gt;
| 169.11&lt;br /&gt;
|-&lt;br /&gt;
| Appearance&lt;br /&gt;
| White Crystalline Solid&lt;br /&gt;
|-&lt;br /&gt;
| CAS registry number|CAS number&lt;br /&gt;
|142-47-2&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Properties&lt;br /&gt;
|-&lt;br /&gt;
| Melting point&lt;br /&gt;
| 232 °C (505 K)&lt;br /&gt;
|-&lt;br /&gt;
| Related compounds &lt;br /&gt;
| Glutamic Acid&lt;br /&gt;
|-&lt;br /&gt;
| Solubility in Water&lt;br /&gt;
| 100 mg/100ml&lt;br /&gt;
|-&lt;br /&gt;
| pH&lt;br /&gt;
| 7.0&lt;br /&gt;
|-&lt;br /&gt;
| {{chembox header}} | &amp;lt;small&amp;gt;Except where noted otherwise, data are given for&amp;lt;br /&amp;gt; materials in their [[standard state|standard state (at 25&amp;amp;nbsp;°C, 100&amp;amp;nbsp;kPa)]]&amp;lt;br /&amp;gt;[[wikipedia:Chemical infobox|Infobox disclaimer and references]]&amp;lt;/small&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
|}&lt;br /&gt;
MSG,is a sodium salt of the amino acid &#039;&#039;&#039;&#039;&#039;L-glutamic acid&#039;&#039;&#039;&#039;&#039;. It is practically odorless. It is produced by a bacterial fermentation process with starch or molasses as carbon sources and ammonium salts as nitrogen sources (Steffen process). MSG is not a direct taste enhancer but a complex flavour enhancer for gravies, meats, poultry, sauces, and in other combinations. It is also used to enhance the taste of tobacco and has been used medically to treat hepatic coma.&lt;br /&gt;
&lt;br /&gt;
==References &amp;amp; Useful Links==&lt;br /&gt;
Image: http://www.germes-online.com/catalog/48/55/189/257161/monosodium_glutamate.html&lt;/div&gt;</summary>
		<author><name>Rw305</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It:MSG&amp;diff=5454</id>
		<title>It:MSG</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It:MSG&amp;diff=5454"/>
		<updated>2006-11-16T14:02:30Z</updated>

		<summary type="html">&lt;p&gt;Rw305: /* The Basics */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;==Abstract==&lt;br /&gt;
&#039;&#039;&#039;Monosodium Glutamate&#039;&#039;&#039; is more commonly known as &#039;&#039;&#039;MSG&#039;&#039;&#039; and has become the choice chemical for the enhancement of flavour in many foods. It was originally discovered in 1909 by the Ajinomoto Corporation in Japan.&lt;br /&gt;
&lt;br /&gt;
==The Basics==&lt;br /&gt;
{| class=&amp;quot;toccolours&amp;quot; border=&amp;quot;1&amp;quot; style=&amp;quot;float: right; clear: right; margin: 0 0 1em 1em; border-collapse: collapse;&amp;quot;&lt;br /&gt;
! {{chembox header}} | MSG &lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; width=&amp;quot;300&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image:msg.jpg]]&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | General&lt;br /&gt;
|-&lt;br /&gt;
| IUPAC nomenclature|Systematic name&lt;br /&gt;
|2-aminopentanedioic acid&lt;br /&gt;
|-&lt;br /&gt;
| Other names&lt;br /&gt;
|2-aminoglutaric acid, 1-aminopropane-1,&lt;br /&gt;
3-dicarboxylic acid&lt;br /&gt;
|-&lt;br /&gt;
| Chemical formula|Molecular formula]&lt;br /&gt;
|C&amp;lt;sub&amp;gt;5&amp;lt;/sub&amp;gt;H&amp;lt;sub&amp;gt;8&amp;lt;/sub&amp;gt;NNaO&amp;lt;sub&amp;gt;4&amp;lt;/sub&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
|-&lt;br /&gt;
| Molecular Weight&lt;br /&gt;
| 169.11&lt;br /&gt;
|-&lt;br /&gt;
| Appearance&lt;br /&gt;
| White Crystalline Solid&lt;br /&gt;
|-&lt;br /&gt;
| CAS registry number|CAS number&lt;br /&gt;
|142-47-2&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Properties&lt;br /&gt;
|-&lt;br /&gt;
| Melting point&lt;br /&gt;
| 232 °C (505 K)&lt;br /&gt;
|-&lt;br /&gt;
| Related compounds &lt;br /&gt;
| Glutamic Acid&lt;br /&gt;
|-&lt;br /&gt;
| Solubility in Water&lt;br /&gt;
| 100 mg/100ml&lt;br /&gt;
|-&lt;br /&gt;
| pH&lt;br /&gt;
| 7.0&lt;br /&gt;
|-&lt;br /&gt;
| {{chembox header}} | &amp;lt;small&amp;gt;Except where noted otherwise, data are given for&amp;lt;br /&amp;gt; materials in their [[standard state|standard state (at 25&amp;amp;nbsp;°C, 100&amp;amp;nbsp;kPa)]]&amp;lt;br /&amp;gt;[[wikipedia:Chemical infobox|Infobox disclaimer and references]]&amp;lt;/small&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
==References &amp;amp; Useful Links==&lt;br /&gt;
Image: http://www.germes-online.com/catalog/48/55/189/257161/monosodium_glutamate.html&lt;/div&gt;</summary>
		<author><name>Rw305</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It:MSG&amp;diff=5453</id>
		<title>It:MSG</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It:MSG&amp;diff=5453"/>
		<updated>2006-11-16T14:02:13Z</updated>

		<summary type="html">&lt;p&gt;Rw305: /* The Basics */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;==Abstract==&lt;br /&gt;
&#039;&#039;&#039;Monosodium Glutamate&#039;&#039;&#039; is more commonly known as &#039;&#039;&#039;MSG&#039;&#039;&#039; and has become the choice chemical for the enhancement of flavour in many foods. It was originally discovered in 1909 by the Ajinomoto Corporation in Japan.&lt;br /&gt;
&lt;br /&gt;
==The Basics==&lt;br /&gt;
{| class=&amp;quot;toccolours&amp;quot; border=&amp;quot;1&amp;quot; style=&amp;quot;float: right; clear: right; margin: 0 0 1em 1em; border-collapse: collapse;&amp;quot;&lt;br /&gt;
! {{chembox header}} | MSG &lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; width=&amp;quot;300&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image:msg.jpg]]&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | General&lt;br /&gt;
|-&lt;br /&gt;
| IUPAC nomenclature|Systematic name&lt;br /&gt;
|2-aminopentanedioic acid&lt;br /&gt;
|-&lt;br /&gt;
| Other names&lt;br /&gt;
|2-aminoglutaric acid, 1-aminopropane-1,&lt;br /&gt;
3-dicarboxylic acid&lt;br /&gt;
|-&lt;br /&gt;
| Chemical formula|Molecular formula]&lt;br /&gt;
|C&amp;lt;sub&amp;gt;5&amp;lt;/sub&amp;gt;H&amp;lt;sub&amp;gt;8&amp;lt;/sub&amp;gt;NNaO&amp;lt;sub&amp;gt;4&amp;lt;/sub&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
|-&lt;br /&gt;
| Molecular Weight&lt;br /&gt;
| 169.11&lt;br /&gt;
|-&lt;br /&gt;
| Appearance&lt;br /&gt;
| White Crystalline Solid&lt;br /&gt;
|-&lt;br /&gt;
| CAS registry number|CAS number&lt;br /&gt;
|142-47-2&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Properties&lt;br /&gt;
|-&lt;br /&gt;
| Melting point&lt;br /&gt;
| 232 °C (505 K)&lt;br /&gt;
|-&lt;br /&gt;
| Related compounds &lt;br /&gt;
| Glutamic Acid&lt;br /&gt;
|-&lt;br /&gt;
| Solubility in Water&lt;br /&gt;
| 100 mg/100ml&lt;br /&gt;
|-&lt;br /&gt;
| pH&lt;br /&gt;
| 7.0&lt;br /&gt;
| {{chembox header}} | &amp;lt;small&amp;gt;Except where noted otherwise, data are given for&amp;lt;br /&amp;gt; materials in their [[standard state|standard state (at 25&amp;amp;nbsp;°C, 100&amp;amp;nbsp;kPa)]]&amp;lt;br /&amp;gt;[[wikipedia:Chemical infobox|Infobox disclaimer and references]]&amp;lt;/small&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
==References &amp;amp; Useful Links==&lt;br /&gt;
Image: http://www.germes-online.com/catalog/48/55/189/257161/monosodium_glutamate.html&lt;/div&gt;</summary>
		<author><name>Rw305</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It:MSG&amp;diff=5452</id>
		<title>It:MSG</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It:MSG&amp;diff=5452"/>
		<updated>2006-11-16T14:00:14Z</updated>

		<summary type="html">&lt;p&gt;Rw305: /* The Basics */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;==Abstract==&lt;br /&gt;
&#039;&#039;&#039;Monosodium Glutamate&#039;&#039;&#039; is more commonly known as &#039;&#039;&#039;MSG&#039;&#039;&#039; and has become the choice chemical for the enhancement of flavour in many foods. It was originally discovered in 1909 by the Ajinomoto Corporation in Japan.&lt;br /&gt;
&lt;br /&gt;
==The Basics==&lt;br /&gt;
{| class=&amp;quot;toccolours&amp;quot; border=&amp;quot;1&amp;quot; style=&amp;quot;float: right; clear: right; margin: 0 0 1em 1em; border-collapse: collapse;&amp;quot;&lt;br /&gt;
! {{chembox header}} | MSG &lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; width=&amp;quot;300&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image:msg.jpg]]&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | General&lt;br /&gt;
|-&lt;br /&gt;
| IUPAC nomenclature|Systematic name&lt;br /&gt;
|2-aminopentanedioic acid&lt;br /&gt;
|-&lt;br /&gt;
| Other names&lt;br /&gt;
|2-aminoglutaric acid, 1-aminopropane-1,&lt;br /&gt;
3-dicarboxylic acid&lt;br /&gt;
|-&lt;br /&gt;
| Chemical formula|Molecular formula]&lt;br /&gt;
|C&amp;lt;sub&amp;gt;5&amp;lt;/sub&amp;gt;H&amp;lt;sub&amp;gt;8&amp;lt;/sub&amp;gt;NNaO&amp;lt;sub&amp;gt;4&amp;lt;/sub&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
|-&lt;br /&gt;
| Molecular Weight&lt;br /&gt;
| 169.11&lt;br /&gt;
|-&lt;br /&gt;
| Appearance&lt;br /&gt;
| White Crystalline Solid&lt;br /&gt;
|-&lt;br /&gt;
| CAS registry number|CAS number&lt;br /&gt;
|142-47-2&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Properties&lt;br /&gt;
|-&lt;br /&gt;
| Melting point&lt;br /&gt;
| 232 °C (505 K)&lt;br /&gt;
|-&lt;br /&gt;
| Related compounds &lt;br /&gt;
| Glutamic Acid&lt;br /&gt;
|-&lt;br /&gt;
| {{chembox header}} | &amp;lt;small&amp;gt;Except where noted otherwise, data are given for&amp;lt;br /&amp;gt; materials in their [[standard state|standard state (at 25&amp;amp;nbsp;°C, 100&amp;amp;nbsp;kPa)]]&amp;lt;br /&amp;gt;[[wikipedia:Chemical infobox|Infobox disclaimer and references]]&amp;lt;/small&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
==References &amp;amp; Useful Links==&lt;br /&gt;
Image: http://www.germes-online.com/catalog/48/55/189/257161/monosodium_glutamate.html&lt;/div&gt;</summary>
		<author><name>Rw305</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It:MSG&amp;diff=5451</id>
		<title>It:MSG</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It:MSG&amp;diff=5451"/>
		<updated>2006-11-16T13:58:05Z</updated>

		<summary type="html">&lt;p&gt;Rw305: /* The Basics */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;==Abstract==&lt;br /&gt;
&#039;&#039;&#039;Monosodium Glutamate&#039;&#039;&#039; is more commonly known as &#039;&#039;&#039;MSG&#039;&#039;&#039; and has become the choice chemical for the enhancement of flavour in many foods. It was originally discovered in 1909 by the Ajinomoto Corporation in Japan.&lt;br /&gt;
&lt;br /&gt;
==The Basics==&lt;br /&gt;
{| class=&amp;quot;toccolours&amp;quot; border=&amp;quot;1&amp;quot; style=&amp;quot;float: right; clear: right; margin: 0 0 1em 1em; border-collapse: collapse;&amp;quot;&lt;br /&gt;
! {{chembox header}} | MSG &lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; width=&amp;quot;300&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image:msg.jpg]]&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | General&lt;br /&gt;
|-&lt;br /&gt;
| [[IUPAC nomenclature|Systematic name]]&lt;br /&gt;
|2-aminopentanedioic acid&lt;br /&gt;
|-&lt;br /&gt;
| Other names&lt;br /&gt;
|2-aminoglutaric acid, 1-aminopropane-1,&lt;br /&gt;
3-dicarboxylic acid&lt;br /&gt;
|-&lt;br /&gt;
| [[Chemical formula|Molecular formula]]&lt;br /&gt;
|C&amp;lt;sub&amp;gt;5&amp;lt;/sub&amp;gt;H&amp;lt;sub&amp;gt;8&amp;lt;/sub&amp;gt;NNaO&amp;lt;sub&amp;gt;4&amp;lt;/sub&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
|-&lt;br /&gt;
| [[Molecular Weight]]&lt;br /&gt;
| 169.11&lt;br /&gt;
|-&lt;br /&gt;
| Appearance&lt;br /&gt;
| White Crystalline Solid&lt;br /&gt;
|-&lt;br /&gt;
| [[CAS registry number|CAS number]]&lt;br /&gt;
|142-47-2&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Properties&lt;br /&gt;
|-&lt;br /&gt;
| [[Melting point]]&lt;br /&gt;
| 232 °C (505 K)&lt;br /&gt;
|-&lt;br /&gt;
| Related compounds &lt;br /&gt;
| Glutamic Acid&lt;br /&gt;
|-&lt;br /&gt;
| {{chembox header}} | &amp;lt;small&amp;gt;Except where noted otherwise, data are given for&amp;lt;br /&amp;gt; materials in their [[standard state|standard state (at 25&amp;amp;nbsp;°C, 100&amp;amp;nbsp;kPa)]]&amp;lt;br /&amp;gt;[[wikipedia:Chemical infobox|Infobox disclaimer and references]]&amp;lt;/small&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
==References &amp;amp; Useful Links==&lt;br /&gt;
Image: http://www.germes-online.com/catalog/48/55/189/257161/monosodium_glutamate.html&lt;/div&gt;</summary>
		<author><name>Rw305</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It:MSG&amp;diff=5450</id>
		<title>It:MSG</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It:MSG&amp;diff=5450"/>
		<updated>2006-11-16T13:55:43Z</updated>

		<summary type="html">&lt;p&gt;Rw305: /* The Basics */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;==Abstract==&lt;br /&gt;
&#039;&#039;&#039;Monosodium Glutamate&#039;&#039;&#039; is more commonly known as &#039;&#039;&#039;MSG&#039;&#039;&#039; and has become the choice chemical for the enhancement of flavour in many foods. It was originally discovered in 1909 by the Ajinomoto Corporation in Japan.&lt;br /&gt;
&lt;br /&gt;
==The Basics==&lt;br /&gt;
{| class=&amp;quot;toccolours&amp;quot; border=&amp;quot;1&amp;quot; style=&amp;quot;float: right; clear: right; margin: 0 0 1em 1em; border-collapse: collapse;&amp;quot;&lt;br /&gt;
! {{chembox header}} | MSG &lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; width=&amp;quot;300&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image:msg.jpg]]&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | General&lt;br /&gt;
|-&lt;br /&gt;
| [[IUPAC nomenclature|Systematic name]]&lt;br /&gt;
|2-aminopentanedioic acid&lt;br /&gt;
|-&lt;br /&gt;
| Other names&lt;br /&gt;
|2-aminoglutaric acid, 1-aminopropane-1,&lt;br /&gt;
3-dicarboxylic acid&lt;br /&gt;
|-&lt;br /&gt;
| [[Chemical formula|Molecular formula]]&lt;br /&gt;
|C&amp;lt;sub&amp;gt;5&amp;lt;/sub&amp;gt;H&amp;lt;sub&amp;gt;8&amp;lt;/sub&amp;gt;NNaO&amp;lt;sub&amp;gt;4&amp;lt;/sub&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
|-&lt;br /&gt;
| [[Molecular Weight]]&lt;br /&gt;
| 169.11&lt;br /&gt;
|-&lt;br /&gt;
| Appearance&lt;br /&gt;
| White Crystalline Solid&lt;br /&gt;
|-&lt;br /&gt;
| [[CAS registry number|CAS number]]&lt;br /&gt;
|142-47-2&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Properties&lt;br /&gt;
|-&lt;br /&gt;
| [[Melting point]]&lt;br /&gt;
| 164-165°C (377-378 K)&lt;br /&gt;
|-&lt;br /&gt;
| Related compounds &lt;br /&gt;
| Sulfadoxine-pyrimethamine&lt;br /&gt;
|-&lt;br /&gt;
| {{chembox header}} | &amp;lt;small&amp;gt;Except where noted otherwise, data are given for&amp;lt;br /&amp;gt; materials in their [[standard state|standard state (at 25&amp;amp;nbsp;°C, 100&amp;amp;nbsp;kPa)]]&amp;lt;br /&amp;gt;[[wikipedia:Chemical infobox|Infobox disclaimer and references]]&amp;lt;/small&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
==References &amp;amp; Useful Links==&lt;br /&gt;
Image: http://www.germes-online.com/catalog/48/55/189/257161/monosodium_glutamate.html&lt;/div&gt;</summary>
		<author><name>Rw305</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It:MSG&amp;diff=5449</id>
		<title>It:MSG</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It:MSG&amp;diff=5449"/>
		<updated>2006-11-16T13:54:07Z</updated>

		<summary type="html">&lt;p&gt;Rw305: /* The Basics */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;==Abstract==&lt;br /&gt;
&#039;&#039;&#039;Monosodium Glutamate&#039;&#039;&#039; is more commonly known as &#039;&#039;&#039;MSG&#039;&#039;&#039; and has become the choice chemical for the enhancement of flavour in many foods. It was originally discovered in 1909 by the Ajinomoto Corporation in Japan.&lt;br /&gt;
&lt;br /&gt;
==The Basics==&lt;br /&gt;
{| class=&amp;quot;toccolours&amp;quot; border=&amp;quot;1&amp;quot; style=&amp;quot;float: right; clear: right; margin: 0 0 1em 1em; border-collapse: collapse;&amp;quot;&lt;br /&gt;
! {{chembox header}} | MSG &lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; width=&amp;quot;300&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image:msg.jpg]]&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | General&lt;br /&gt;
|-&lt;br /&gt;
| [[IUPAC nomenclature|Systematic name]]&lt;br /&gt;
|2-aminopentanedioic acid&lt;br /&gt;
|-&lt;br /&gt;
| Other names&lt;br /&gt;
|2-aminoglutaric acid, 1-aminopropane-1,&lt;br /&gt;
3-dicarboxylic acid&lt;br /&gt;
|-&lt;br /&gt;
| [[Chemical formula|Molecular formula]]&lt;br /&gt;
|C&amp;lt;sub&amp;gt;5&amp;lt;/sub&amp;gt;H&amp;lt;sub&amp;gt;8&amp;lt;/sub&amp;gt;NNaO&amp;lt;sub&amp;gt;4&amp;lt;/sub&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
|-&lt;br /&gt;
| [[Molecular Weight]]&lt;br /&gt;
| 169.11&lt;br /&gt;
|-&lt;br /&gt;
| Appearance&lt;br /&gt;
| White Crystalline Solid&lt;br /&gt;
|-&lt;br /&gt;
| [[CAS registry number|CAS number]]&lt;br /&gt;
| 32221-81-1&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Properties&lt;br /&gt;
|-&lt;br /&gt;
| [[Melting point]]&lt;br /&gt;
| 164-165°C (377-378 K)&lt;br /&gt;
|-&lt;br /&gt;
| Related compounds &lt;br /&gt;
| Sulfadoxine-pyrimethamine&lt;br /&gt;
|-&lt;br /&gt;
| {{chembox header}} | &amp;lt;small&amp;gt;Except where noted otherwise, data are given for&amp;lt;br /&amp;gt; materials in their [[standard state|standard state (at 25&amp;amp;nbsp;°C, 100&amp;amp;nbsp;kPa)]]&amp;lt;br /&amp;gt;[[wikipedia:Chemical infobox|Infobox disclaimer and references]]&amp;lt;/small&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
==References &amp;amp; Useful Links==&lt;br /&gt;
Image: http://www.germes-online.com/catalog/48/55/189/257161/monosodium_glutamate.html&lt;/div&gt;</summary>
		<author><name>Rw305</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It:MSG&amp;diff=5448</id>
		<title>It:MSG</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It:MSG&amp;diff=5448"/>
		<updated>2006-11-16T13:52:29Z</updated>

		<summary type="html">&lt;p&gt;Rw305: /* References &amp;amp; Links */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;==Abstract==&lt;br /&gt;
&#039;&#039;&#039;Monosodium Glutamate&#039;&#039;&#039; is more commonly known as &#039;&#039;&#039;MSG&#039;&#039;&#039; and has become the choice chemical for the enhancement of flavour in many foods. It was originally discovered in 1909 by the Ajinomoto Corporation in Japan.&lt;br /&gt;
&lt;br /&gt;
==The Basics==&lt;br /&gt;
{| class=&amp;quot;toccolours&amp;quot; border=&amp;quot;1&amp;quot; style=&amp;quot;float: right; clear: right; margin: 0 0 1em 1em; border-collapse: collapse;&amp;quot;&lt;br /&gt;
! {{chembox header}} | MSG &lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; width=&amp;quot;300&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image:msg.jpg]]&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | General&lt;br /&gt;
|-&lt;br /&gt;
| [[IUPAC nomenclature|Systematic name]]&lt;br /&gt;
|2-aminopentanedioic acid&lt;br /&gt;
|-&lt;br /&gt;
| Other names&lt;br /&gt;
|2-aminoglutaric acid, 1-aminopropane-1,&lt;br /&gt;
3-dicarboxylic acid&lt;br /&gt;
|-&lt;br /&gt;
| [[Chemical formula|Molecular formula]]&lt;br /&gt;
|C&amp;lt;sub&amp;gt;5&amp;lt;/sub&amp;gt;H&amp;lt;sub&amp;gt;8&amp;lt;/sub&amp;gt;NNaO&amp;lt;sub&amp;gt;4&amp;lt;/sub&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
|-&lt;br /&gt;
| [[Molecular Weight]]&lt;br /&gt;
| 169.11&lt;br /&gt;
|-&lt;br /&gt;
| Appearance&lt;br /&gt;
| White Crystalline Solid&lt;br /&gt;
|-&lt;br /&gt;
| [[CAS registry number|CAS number]]&lt;br /&gt;
| 142-47-2&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Properties&lt;br /&gt;
|-&lt;br /&gt;
| [[Melting point]]&lt;br /&gt;
| 164-165°C (377-378 K)&lt;br /&gt;
|-&lt;br /&gt;
| Related compounds &lt;br /&gt;
| Sulfadoxine-pyrimethamine&lt;br /&gt;
|-&lt;br /&gt;
| {{chembox header}} | &amp;lt;small&amp;gt;Except where noted otherwise, data are given for&amp;lt;br /&amp;gt; materials in their [[standard state|standard state (at 25&amp;amp;nbsp;°C, 100&amp;amp;nbsp;kPa)]]&amp;lt;br /&amp;gt;[[wikipedia:Chemical infobox|Infobox disclaimer and references]]&amp;lt;/small&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==References &amp;amp; Useful Links==&lt;br /&gt;
Image: http://www.germes-online.com/catalog/48/55/189/257161/monosodium_glutamate.html&lt;/div&gt;</summary>
		<author><name>Rw305</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It:MSG&amp;diff=5447</id>
		<title>It:MSG</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It:MSG&amp;diff=5447"/>
		<updated>2006-11-16T13:50:59Z</updated>

		<summary type="html">&lt;p&gt;Rw305: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;==Abstract==&lt;br /&gt;
&#039;&#039;&#039;Monosodium Glutamate&#039;&#039;&#039; is more commonly known as &#039;&#039;&#039;MSG&#039;&#039;&#039; and has become the choice chemical for the enhancement of flavour in many foods. It was originally discovered in 1909 by the Ajinomoto Corporation in Japan.&lt;br /&gt;
&lt;br /&gt;
==The Basics==&lt;br /&gt;
{| class=&amp;quot;toccolours&amp;quot; border=&amp;quot;1&amp;quot; style=&amp;quot;float: right; clear: right; margin: 0 0 1em 1em; border-collapse: collapse;&amp;quot;&lt;br /&gt;
! {{chembox header}} | MSG &lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; width=&amp;quot;300&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image:msg.jpg]]&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | General&lt;br /&gt;
|-&lt;br /&gt;
| [[IUPAC nomenclature|Systematic name]]&lt;br /&gt;
|2-aminopentanedioic acid&lt;br /&gt;
|-&lt;br /&gt;
| Other names&lt;br /&gt;
|2-aminoglutaric acid, 1-aminopropane-1,&lt;br /&gt;
3-dicarboxylic acid&lt;br /&gt;
|-&lt;br /&gt;
| [[Chemical formula|Molecular formula]]&lt;br /&gt;
|C&amp;lt;sub&amp;gt;5&amp;lt;/sub&amp;gt;H&amp;lt;sub&amp;gt;8&amp;lt;/sub&amp;gt;NNaO&amp;lt;sub&amp;gt;4&amp;lt;/sub&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
|-&lt;br /&gt;
| [[Molecular Weight]]&lt;br /&gt;
| 169.11&lt;br /&gt;
|-&lt;br /&gt;
| Appearance&lt;br /&gt;
| White Crystalline Solid&lt;br /&gt;
|-&lt;br /&gt;
| [[CAS registry number|CAS number]]&lt;br /&gt;
| 142-47-2&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Properties&lt;br /&gt;
|-&lt;br /&gt;
| [[Melting point]]&lt;br /&gt;
| 164-165°C (377-378 K)&lt;br /&gt;
|-&lt;br /&gt;
| Related compounds &lt;br /&gt;
| Sulfadoxine-pyrimethamine&lt;br /&gt;
|-&lt;br /&gt;
| {{chembox header}} | &amp;lt;small&amp;gt;Except where noted otherwise, data are given for&amp;lt;br /&amp;gt; materials in their [[standard state|standard state (at 25&amp;amp;nbsp;°C, 100&amp;amp;nbsp;kPa)]]&amp;lt;br /&amp;gt;[[wikipedia:Chemical infobox|Infobox disclaimer and references]]&amp;lt;/small&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==References &amp;amp; Links==&lt;br /&gt;
Image: http://www.germes-online.com/catalog/48/55/189/257161/monosodium_glutamate.html&lt;/div&gt;</summary>
		<author><name>Rw305</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It:MSG&amp;diff=5446</id>
		<title>It:MSG</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It:MSG&amp;diff=5446"/>
		<updated>2006-11-16T13:49:25Z</updated>

		<summary type="html">&lt;p&gt;Rw305: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;==Abstract==&lt;br /&gt;
&#039;&#039;&#039;Monosodium Glutamate&#039;&#039;&#039; is more commonly known as &#039;&#039;&#039;MSG&#039;&#039;&#039; and has become the choice chemical for the enhancement of flavour in many foods. It was originally discovered in 1909 by the Ajinomoto Corporation in Japan.&lt;br /&gt;
&lt;br /&gt;
==The Basics==&lt;br /&gt;
{| class=&amp;quot;toccolours&amp;quot; border=&amp;quot;1&amp;quot; style=&amp;quot;float: right; clear: right; margin: 0 0 1em 1em; border-collapse: collapse;&amp;quot;&lt;br /&gt;
! {{chembox header}} | MSG &lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; width=&amp;quot;300&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image:msg.jpg]]&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | General&lt;br /&gt;
|-&lt;br /&gt;
| [[IUPAC nomenclature|Systematic name]]&lt;br /&gt;
|2-aminopentanedioic acid&lt;br /&gt;
|-&lt;br /&gt;
| Other names&lt;br /&gt;
|2-aminoglutaric acid, 1-aminopropane-1,&lt;br /&gt;
3-dicarboxylic acid&lt;br /&gt;
|-&lt;br /&gt;
| [[Chemical formula|Molecular formula]]&lt;br /&gt;
|C&amp;lt;sub&amp;gt;5&amp;lt;/sub&amp;gt;H&amp;lt;sub&amp;gt;8&amp;lt;/sub&amp;gt;NNaO&amp;lt;sub&amp;gt;4&amp;lt;/sub&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
|-&lt;br /&gt;
| [[Molecular Weight]]&lt;br /&gt;
| 169.11&lt;br /&gt;
|-&lt;br /&gt;
| Appearance&lt;br /&gt;
| White Crystalline Solid&lt;br /&gt;
|-&lt;br /&gt;
| [[CAS registry number|CAS number]]&lt;br /&gt;
| 142-47-2&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Properties&lt;br /&gt;
|-&lt;br /&gt;
| [[Melting point]]&lt;br /&gt;
| 164-165°C (377-378 K)&lt;br /&gt;
|-&lt;br /&gt;
| Related compounds &lt;br /&gt;
| Sulfadoxine-pyrimethamine&lt;br /&gt;
|-&lt;br /&gt;
| {{chembox header}} | &amp;lt;small&amp;gt;Except where noted otherwise, data are given for&amp;lt;br /&amp;gt; materials in their [[standard state|standard state (at 25&amp;amp;nbsp;°C, 100&amp;amp;nbsp;kPa)]]&amp;lt;br /&amp;gt;[[wikipedia:Chemical infobox|Infobox disclaimer and references]]&amp;lt;/small&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
==References &amp;amp; Links==&lt;br /&gt;
Image: http://www.germes-online.com/catalog/48/55/189/257161/monosodium_glutamate.html&lt;/div&gt;</summary>
		<author><name>Rw305</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It:MSG&amp;diff=5445</id>
		<title>It:MSG</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It:MSG&amp;diff=5445"/>
		<updated>2006-11-16T13:47:15Z</updated>

		<summary type="html">&lt;p&gt;Rw305: /* The Basics */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;==Abstract==&lt;br /&gt;
&#039;&#039;&#039;Monosodium Glutamate&#039;&#039;&#039; is more commonly known as &#039;&#039;&#039;MSG&#039;&#039;&#039; and has become the choice chemical for the enhancement of flavour in many foods. It was originally discovered in 1909 by the Ajinomoto Corporation in Japan.&lt;br /&gt;
&lt;br /&gt;
==The Basics==&lt;br /&gt;
{| class=&amp;quot;toccolours&amp;quot; border=&amp;quot;1&amp;quot; style=&amp;quot;float: right; clear: right; margin: 0 0 1em 1em; border-collapse: collapse;&amp;quot;&lt;br /&gt;
! {{chembox header}} | MSG &lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; width=&amp;quot;300&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image:msg.jpg]]&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | General&lt;br /&gt;
|-&lt;br /&gt;
| [[IUPAC nomenclature|Systematic name]]&lt;br /&gt;
|2-aminopentanedioic acid&lt;br /&gt;
|-&lt;br /&gt;
| Other names&lt;br /&gt;
|2-aminoglutaric acid, 1-aminopropane-1,&lt;br /&gt;
3-dicarboxylic acid&lt;br /&gt;
|-&lt;br /&gt;
| [[Chemical formula|Molecular formula]]&lt;br /&gt;
|C&amp;lt;sub&amp;gt;5&amp;lt;/sub&amp;gt;H&amp;lt;sub&amp;gt;8&amp;lt;/sub&amp;gt;NNaO&amp;lt;sub&amp;gt;4&amp;lt;/sub&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
|-&lt;br /&gt;
| [[Molecular Weight]]&lt;br /&gt;
| 169.11&lt;br /&gt;
|-&lt;br /&gt;
| Appearance&lt;br /&gt;
| White Crystalline Solid&lt;br /&gt;
|-&lt;br /&gt;
| [[CAS registry number|CAS number]]&lt;br /&gt;
| 142-47-2&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Properties&lt;br /&gt;
|-&lt;br /&gt;
| [[Melting point]]&lt;br /&gt;
| 164-165°C (377-378 K)&lt;br /&gt;
|-&lt;br /&gt;
| Related compounds &lt;br /&gt;
| Sulfadoxine-pyrimethamine&lt;br /&gt;
|-&lt;br /&gt;
| {{chembox header}} | &amp;lt;small&amp;gt;Except where noted otherwise, data are given for&amp;lt;br /&amp;gt; materials in their [[standard state|standard state (at 25&amp;amp;nbsp;°C, 100&amp;amp;nbsp;kPa)]]&amp;lt;br /&amp;gt;[[wikipedia:Chemical infobox|Infobox disclaimer and references]]&amp;lt;/small&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
|}&lt;/div&gt;</summary>
		<author><name>Rw305</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=File:Msg.jpg&amp;diff=5444</id>
		<title>File:Msg.jpg</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=File:Msg.jpg&amp;diff=5444"/>
		<updated>2006-11-16T13:45:22Z</updated>

		<summary type="html">&lt;p&gt;Rw305: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;/div&gt;</summary>
		<author><name>Rw305</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It:MSG&amp;diff=5443</id>
		<title>It:MSG</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It:MSG&amp;diff=5443"/>
		<updated>2006-11-16T13:44:55Z</updated>

		<summary type="html">&lt;p&gt;Rw305: /* The Basics */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;==Abstract==&lt;br /&gt;
&#039;&#039;&#039;Monosodium Glutamate&#039;&#039;&#039; is more commonly known as &#039;&#039;&#039;MSG&#039;&#039;&#039; and has become the choice chemical for the enhancement of flavour in many foods. It was originally discovered in 1909 by the Ajinomoto Corporation in Japan.&lt;br /&gt;
&lt;br /&gt;
==The Basics==&lt;br /&gt;
{| class=&amp;quot;toccolours&amp;quot; border=&amp;quot;1&amp;quot; style=&amp;quot;float: right; clear: right; margin: 0 0 1em 1em; border-collapse: collapse;&amp;quot;&lt;br /&gt;
! {{chembox header}} | MSG &lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; width=&amp;quot;300&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image:msg.jpg|thumb|]]&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | General&lt;br /&gt;
|-&lt;br /&gt;
| [[IUPAC nomenclature|Systematic name]]&lt;br /&gt;
|2-aminopentanedioic acid&lt;br /&gt;
|-&lt;br /&gt;
| Other names&lt;br /&gt;
|2-aminoglutaric acid, 1-aminopropane-1,&lt;br /&gt;
3-dicarboxylic acid&lt;br /&gt;
|-&lt;br /&gt;
| [[Chemical formula|Molecular formula]]&lt;br /&gt;
|C&amp;lt;sub&amp;gt;5&amp;lt;/sub&amp;gt;H&amp;lt;sub&amp;gt;8&amp;lt;/sub&amp;gt;NNaO&amp;lt;sub&amp;gt;4&amp;lt;/sub&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
|-&lt;br /&gt;
| [[Molecular Weight]]&lt;br /&gt;
| 169.11&lt;br /&gt;
|-&lt;br /&gt;
| Appearance&lt;br /&gt;
| White Crystalline Solid&lt;br /&gt;
|-&lt;br /&gt;
| [[CAS registry number|CAS number]]&lt;br /&gt;
| 142-47-2&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Properties&lt;br /&gt;
|-&lt;br /&gt;
| [[Melting point]]&lt;br /&gt;
| 164-165°C (377-378 K)&lt;br /&gt;
|-&lt;br /&gt;
| Related compounds &lt;br /&gt;
| Sulfadoxine-pyrimethamine&lt;br /&gt;
|-&lt;br /&gt;
| {{chembox header}} | &amp;lt;small&amp;gt;Except where noted otherwise, data are given for&amp;lt;br /&amp;gt; materials in their [[standard state|standard state (at 25&amp;amp;nbsp;°C, 100&amp;amp;nbsp;kPa)]]&amp;lt;br /&amp;gt;[[wikipedia:Chemical infobox|Infobox disclaimer and references]]&amp;lt;/small&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
|}&lt;/div&gt;</summary>
		<author><name>Rw305</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It:MSG&amp;diff=5442</id>
		<title>It:MSG</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It:MSG&amp;diff=5442"/>
		<updated>2006-11-16T12:24:23Z</updated>

		<summary type="html">&lt;p&gt;Rw305: /* The Basics */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;==Abstract==&lt;br /&gt;
&#039;&#039;&#039;Monosodium Glutamate&#039;&#039;&#039; is more commonly known as &#039;&#039;&#039;MSG&#039;&#039;&#039; and has become the choice chemical for the enhancement of flavour in many foods. It was originally discovered in 1909 by the Ajinomoto Corporation in Japan.&lt;br /&gt;
&lt;br /&gt;
==The Basics==&lt;br /&gt;
{| class=&amp;quot;toccolours&amp;quot; border=&amp;quot;1&amp;quot; style=&amp;quot;float: right; clear: right; margin: 0 0 1em 1em; border-collapse: collapse;&amp;quot;&lt;br /&gt;
! {{chembox header}} | MSG &lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; width=&amp;quot;300&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image:It-Dihydroartemisinin.jpg|thumb|]]&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | General&lt;br /&gt;
|-&lt;br /&gt;
| [[IUPAC nomenclature|Systematic name]]&lt;br /&gt;
|2-aminopentanedioic acid&lt;br /&gt;
|-&lt;br /&gt;
| Other names&lt;br /&gt;
|2-aminoglutaric acid, 1-aminopropane-1,&lt;br /&gt;
3-dicarboxylic acid&lt;br /&gt;
|-&lt;br /&gt;
| [[Chemical formula|Molecular formula]]&lt;br /&gt;
|C&amp;lt;sub&amp;gt;5&amp;lt;/sub&amp;gt;H&amp;lt;sub&amp;gt;8&amp;lt;/sub&amp;gt;NNaO&amp;lt;sub&amp;gt;4&amp;lt;/sub&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
|-&lt;br /&gt;
| [[Molecular Weight]]&lt;br /&gt;
| 169.11&lt;br /&gt;
|-&lt;br /&gt;
| Appearance&lt;br /&gt;
| White Crystalline Solid&lt;br /&gt;
|-&lt;br /&gt;
| [[CAS registry number|CAS number]]&lt;br /&gt;
| 142-47-2&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Properties&lt;br /&gt;
|-&lt;br /&gt;
| [[Melting point]]&lt;br /&gt;
| 164-165°C (377-378 K)&lt;br /&gt;
|-&lt;br /&gt;
| Related compounds &lt;br /&gt;
| Sulfadoxine-pyrimethamine&lt;br /&gt;
|-&lt;br /&gt;
| {{chembox header}} | &amp;lt;small&amp;gt;Except where noted otherwise, data are given for&amp;lt;br /&amp;gt; materials in their [[standard state|standard state (at 25&amp;amp;nbsp;°C, 100&amp;amp;nbsp;kPa)]]&amp;lt;br /&amp;gt;[[wikipedia:Chemical infobox|Infobox disclaimer and references]]&amp;lt;/small&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
|}&lt;/div&gt;</summary>
		<author><name>Rw305</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It:MSG&amp;diff=5441</id>
		<title>It:MSG</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It:MSG&amp;diff=5441"/>
		<updated>2006-11-16T12:17:59Z</updated>

		<summary type="html">&lt;p&gt;Rw305: /* The Basics */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;==Abstract==&lt;br /&gt;
&#039;&#039;&#039;Monosodium Glutamate&#039;&#039;&#039; is more commonly known as &#039;&#039;&#039;MSG&#039;&#039;&#039; and has become the choice chemical for the enhancement of flavour in many foods. It was originally discovered in 1909 by the Ajinomoto Corporation in Japan.&lt;br /&gt;
&lt;br /&gt;
==The Basics==&lt;br /&gt;
{| class=&amp;quot;toccolours&amp;quot; border=&amp;quot;1&amp;quot; style=&amp;quot;float: right; clear: right; margin: 0 0 1em 1em; border-collapse: collapse;&amp;quot;&lt;br /&gt;
! {{chembox header}} | MSG &lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; width=&amp;quot;300&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image:It-Dihydroartemisinin.jpg|thumb|]]&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | General&lt;br /&gt;
|-&lt;br /&gt;
| [[IUPAC nomenclature|Systematic name]]&lt;br /&gt;
|2-aminopentanedioic acid&lt;br /&gt;
|-&lt;br /&gt;
| Other names&lt;br /&gt;
|2-aminoglutaric acid, 1-aminopropane-1,&lt;br /&gt;
3-dicarboxylic acid&lt;br /&gt;
|-&lt;br /&gt;
| [[Chemical formula|Molecular formula]]&lt;br /&gt;
|C&amp;lt;sub&amp;gt;5&amp;lt;/sub&amp;gt;H&amp;lt;sub&amp;gt;8&amp;lt;/sub&amp;gt;NNaO&amp;lt;sub&amp;gt;4&amp;lt;/sub&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
|-&lt;br /&gt;
| [[Molecular Weight]]&lt;br /&gt;
| 169.11&lt;br /&gt;
|-&lt;br /&gt;
| Appearance&lt;br /&gt;
| White Crystalline Solid&lt;br /&gt;
|-&lt;br /&gt;
| [[CAS registry number|CAS number]]&lt;br /&gt;
| 81496-82-4&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Properties&lt;br /&gt;
|-&lt;br /&gt;
| [[Melting point]]&lt;br /&gt;
| 164-165°C (377-378 K)&lt;br /&gt;
|-&lt;br /&gt;
| Related compounds &lt;br /&gt;
| Sulfadoxine-pyrimethamine&lt;br /&gt;
|-&lt;br /&gt;
| {{chembox header}} | &amp;lt;small&amp;gt;Except where noted otherwise, data are given for&amp;lt;br /&amp;gt; materials in their [[standard state|standard state (at 25&amp;amp;nbsp;°C, 100&amp;amp;nbsp;kPa)]]&amp;lt;br /&amp;gt;[[wikipedia:Chemical infobox|Infobox disclaimer and references]]&amp;lt;/small&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
|}&lt;/div&gt;</summary>
		<author><name>Rw305</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It:MSG&amp;diff=5440</id>
		<title>It:MSG</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It:MSG&amp;diff=5440"/>
		<updated>2006-11-16T12:17:51Z</updated>

		<summary type="html">&lt;p&gt;Rw305: /* The Basics */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;==Abstract==&lt;br /&gt;
&#039;&#039;&#039;Monosodium Glutamate&#039;&#039;&#039; is more commonly known as &#039;&#039;&#039;MSG&#039;&#039;&#039; and has become the choice chemical for the enhancement of flavour in many foods. It was originally discovered in 1909 by the Ajinomoto Corporation in Japan.&lt;br /&gt;
&lt;br /&gt;
==The Basics==&lt;br /&gt;
{| class=&amp;quot;toccolours&amp;quot; border=&amp;quot;1&amp;quot; style=&amp;quot;float: right; clear: right; margin: 0 0 1em 1em; border-collapse: collapse;&amp;quot;&lt;br /&gt;
! {{chembox header}} | MSG &lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; width=&amp;quot;300&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffgf&amp;quot; | [[Image:It-Dihydroartemisinin.jpg|thumb|]]&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | General&lt;br /&gt;
|-&lt;br /&gt;
| [[IUPAC nomenclature|Systematic name]]&lt;br /&gt;
|2-aminopentanedioic acid&lt;br /&gt;
|-&lt;br /&gt;
| Other names&lt;br /&gt;
|2-aminoglutaric acid, 1-aminopropane-1,&lt;br /&gt;
3-dicarboxylic acid&lt;br /&gt;
|-&lt;br /&gt;
| [[Chemical formula|Molecular formula]]&lt;br /&gt;
|C&amp;lt;sub&amp;gt;5&amp;lt;/sub&amp;gt;H&amp;lt;sub&amp;gt;8&amp;lt;/sub&amp;gt;NNaO&amp;lt;sub&amp;gt;4&amp;lt;/sub&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
|-&lt;br /&gt;
| [[Molecular Weight]]&lt;br /&gt;
| 169.11&lt;br /&gt;
|-&lt;br /&gt;
| Appearance&lt;br /&gt;
| White Crystalline Solid&lt;br /&gt;
|-&lt;br /&gt;
| [[CAS registry number|CAS number]]&lt;br /&gt;
| 81496-82-4&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Properties&lt;br /&gt;
|-&lt;br /&gt;
| [[Melting point]]&lt;br /&gt;
| 164-165°C (377-378 K)&lt;br /&gt;
|-&lt;br /&gt;
| Related compounds &lt;br /&gt;
| Sulfadoxine-pyrimethamine&lt;br /&gt;
|-&lt;br /&gt;
| {{chembox header}} | &amp;lt;small&amp;gt;Except where noted otherwise, data are given for&amp;lt;br /&amp;gt; materials in their [[standard state|standard state (at 25&amp;amp;nbsp;°C, 100&amp;amp;nbsp;kPa)]]&amp;lt;br /&amp;gt;[[wikipedia:Chemical infobox|Infobox disclaimer and references]]&amp;lt;/small&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
|}&lt;/div&gt;</summary>
		<author><name>Rw305</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It:MSG&amp;diff=5439</id>
		<title>It:MSG</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It:MSG&amp;diff=5439"/>
		<updated>2006-11-16T12:17:41Z</updated>

		<summary type="html">&lt;p&gt;Rw305: /* The Basics */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;==Abstract==&lt;br /&gt;
&#039;&#039;&#039;Monosodium Glutamate&#039;&#039;&#039; is more commonly known as &#039;&#039;&#039;MSG&#039;&#039;&#039; and has become the choice chemical for the enhancement of flavour in many foods. It was originally discovered in 1909 by the Ajinomoto Corporation in Japan.&lt;br /&gt;
&lt;br /&gt;
==The Basics==&lt;br /&gt;
{| class=&amp;quot;toccolours&amp;quot; border=&amp;quot;1&amp;quot; style=&amp;quot;float: right; clear: right; margin: 0 0 1em 1em; border-collapse: collapse;&amp;quot;&lt;br /&gt;
! {{chembox header}} | MSG &lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; width=&amp;quot;300&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image:It-Dihydroartemisinin.jpg|thumb|]]&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | General&lt;br /&gt;
|-&lt;br /&gt;
| [[IUPAC nomenclature|Systematic name]]&lt;br /&gt;
|2-aminopentanedioic acid&lt;br /&gt;
|-&lt;br /&gt;
| Other names&lt;br /&gt;
|2-aminoglutaric acid, 1-aminopropane-1,&lt;br /&gt;
3-dicarboxylic acid&lt;br /&gt;
|-&lt;br /&gt;
| [[Chemical formula|Molecular formula]]&lt;br /&gt;
|C&amp;lt;sub&amp;gt;5&amp;lt;/sub&amp;gt;H&amp;lt;sub&amp;gt;8&amp;lt;/sub&amp;gt;NNaO&amp;lt;sub&amp;gt;4&amp;lt;/sub&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
|-&lt;br /&gt;
| [[Molecular Weight]]&lt;br /&gt;
| 169.11&lt;br /&gt;
|-&lt;br /&gt;
| Appearance&lt;br /&gt;
| White Crystalline Solid&lt;br /&gt;
|-&lt;br /&gt;
| [[CAS registry number|CAS number]]&lt;br /&gt;
| 81496-82-4&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Properties&lt;br /&gt;
|-&lt;br /&gt;
| [[Melting point]]&lt;br /&gt;
| 164-165°C (377-378 K)&lt;br /&gt;
|-&lt;br /&gt;
| Related compounds &lt;br /&gt;
| Sulfadoxine-pyrimethamine&lt;br /&gt;
|-&lt;br /&gt;
| {{chembox header}} | &amp;lt;small&amp;gt;Except where noted otherwise, data are given for&amp;lt;br /&amp;gt; materials in their [[standard state|standard state (at 25&amp;amp;nbsp;°C, 100&amp;amp;nbsp;kPa)]]&amp;lt;br /&amp;gt;[[wikipedia:Chemical infobox|Infobox disclaimer and references]]&amp;lt;/small&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
|}&lt;/div&gt;</summary>
		<author><name>Rw305</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It:MSG&amp;diff=5438</id>
		<title>It:MSG</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It:MSG&amp;diff=5438"/>
		<updated>2006-11-16T12:17:14Z</updated>

		<summary type="html">&lt;p&gt;Rw305: /* The Basics */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;==Abstract==&lt;br /&gt;
&#039;&#039;&#039;Monosodium Glutamate&#039;&#039;&#039; is more commonly known as &#039;&#039;&#039;MSG&#039;&#039;&#039; and has become the choice chemical for the enhancement of flavour in many foods. It was originally discovered in 1909 by the Ajinomoto Corporation in Japan.&lt;br /&gt;
&lt;br /&gt;
==The Basics==&lt;br /&gt;
{| class=&amp;quot;toccolours&amp;quot; border=&amp;quot;1&amp;quot; style=&amp;quot;float: right; clear: right; margin: 0 0 1em 1em; border-collapse: collapse;&amp;quot;&lt;br /&gt;
! {{chembox header}} | {{PAGENAME}} &amp;lt;!-- replace if not identical with the article name --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; width=&amp;quot;300&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image:It-Dihydroartemisinin.jpg|thumb|]]&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | General&lt;br /&gt;
|-&lt;br /&gt;
| [[IUPAC nomenclature|Systematic name]]&lt;br /&gt;
|2-aminopentanedioic acid&lt;br /&gt;
|-&lt;br /&gt;
| Other names&lt;br /&gt;
|2-aminoglutaric acid, 1-aminopropane-1,&lt;br /&gt;
3-dicarboxylic acid&lt;br /&gt;
|-&lt;br /&gt;
| [[Chemical formula|Molecular formula]]&lt;br /&gt;
|C&amp;lt;sub&amp;gt;5&amp;lt;/sub&amp;gt;H&amp;lt;sub&amp;gt;8&amp;lt;/sub&amp;gt;NNaO&amp;lt;sub&amp;gt;4&amp;lt;/sub&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
|-&lt;br /&gt;
| [[Molecular Weight]]&lt;br /&gt;
| 169.11&lt;br /&gt;
|-&lt;br /&gt;
| Appearance&lt;br /&gt;
| White Crystalline Solid&lt;br /&gt;
|-&lt;br /&gt;
| [[CAS registry number|CAS number]]&lt;br /&gt;
| 81496-82-4&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Properties&lt;br /&gt;
|-&lt;br /&gt;
| [[Melting point]]&lt;br /&gt;
| 164-165°C (377-378 K)&lt;br /&gt;
|-&lt;br /&gt;
| Related compounds &lt;br /&gt;
| Sulfadoxine-pyrimethamine&lt;br /&gt;
|-&lt;br /&gt;
| {{chembox header}} | &amp;lt;small&amp;gt;Except where noted otherwise, data are given for&amp;lt;br /&amp;gt; materials in their [[standard state|standard state (at 25&amp;amp;nbsp;°C, 100&amp;amp;nbsp;kPa)]]&amp;lt;br /&amp;gt;[[wikipedia:Chemical infobox|Infobox disclaimer and references]]&amp;lt;/small&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
|}&lt;/div&gt;</summary>
		<author><name>Rw305</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It:MSG&amp;diff=5437</id>
		<title>It:MSG</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It:MSG&amp;diff=5437"/>
		<updated>2006-11-16T12:14:52Z</updated>

		<summary type="html">&lt;p&gt;Rw305: /* The Basics */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;==Abstract==&lt;br /&gt;
&#039;&#039;&#039;Monosodium Glutamate&#039;&#039;&#039; is more commonly known as &#039;&#039;&#039;MSG&#039;&#039;&#039; and has become the choice chemical for the enhancement of flavour in many foods. It was originally discovered in 1909 by the Ajinomoto Corporation in Japan.&lt;br /&gt;
&lt;br /&gt;
==The Basics==&lt;br /&gt;
{| class=&amp;quot;toccolours&amp;quot; border=&amp;quot;1&amp;quot; style=&amp;quot;float: right; clear: right; margin: 0 0 1em 1em; border-collapse: collapse;&amp;quot;&lt;br /&gt;
! {{chembox header}} | {{PAGENAME}} &amp;lt;!-- replace if not identical with the article name --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; width=&amp;quot;300&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image:It-Dihydroartemisinin.jpg|thumb|]]&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | General&lt;br /&gt;
|-&lt;br /&gt;
| [[IUPAC nomenclature|Systematic name]]&lt;br /&gt;
|2-aminopentanedioic acid&lt;br /&gt;
|-&lt;br /&gt;
| Other names&lt;br /&gt;
|2-aminoglutaric acid, 1-aminopropane-1,3-dicarboxylic acid&lt;br /&gt;
|-&lt;br /&gt;
| [[Chemical formula|Molecular formula]]&lt;br /&gt;
|C&amp;lt;sub&amp;gt;5&amp;lt;/sub&amp;gt;H&amp;lt;sub&amp;gt;8&amp;lt;/sub&amp;gt;NNaO&amp;lt;sub&amp;gt;4&amp;lt;/sub&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
|-&lt;br /&gt;
| [[Molecular Weight]]&lt;br /&gt;
| 169.11&lt;br /&gt;
|-&lt;br /&gt;
| Appearance&lt;br /&gt;
| White Crystalline Solid&lt;br /&gt;
|-&lt;br /&gt;
| [[CAS registry number|CAS number]]&lt;br /&gt;
| 81496-82-4&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Properties&lt;br /&gt;
|-&lt;br /&gt;
| [[Melting point]]&lt;br /&gt;
| 164-165°C (377-378 K)&lt;br /&gt;
|-&lt;br /&gt;
| Related compounds &lt;br /&gt;
| Sulfadoxine-pyrimethamine&lt;br /&gt;
|-&lt;br /&gt;
| {{chembox header}} | &amp;lt;small&amp;gt;Except where noted otherwise, data are given for&amp;lt;br /&amp;gt; materials in their [[standard state|standard state (at 25&amp;amp;nbsp;°C, 100&amp;amp;nbsp;kPa)]]&amp;lt;br /&amp;gt;[[wikipedia:Chemical infobox|Infobox disclaimer and references]]&amp;lt;/small&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
|}&lt;/div&gt;</summary>
		<author><name>Rw305</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It:Dihydroartemisinin&amp;diff=5436</id>
		<title>It:Dihydroartemisinin</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It:Dihydroartemisinin&amp;diff=5436"/>
		<updated>2006-11-16T12:00:14Z</updated>

		<summary type="html">&lt;p&gt;Rw305: /* Basic Information */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;== Abstract ==&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;Dihydroartemisinin&#039;&#039;&#039; is the active ingredient in the anti-malarial drugs Alaxin and Cotexin. The parasitic disease is transferred through mosquito bites &amp;amp; in many cases fatal and over the years has become more and more resistant to drugs designed to counter its effects. The disease is most present in tropical countries such as Brazil, India, Thailand and Nigeria due to the the high mosquito population.&lt;br /&gt;
&lt;br /&gt;
== Basic Information ==&lt;br /&gt;
{| class=&amp;quot;toccolours&amp;quot; border=&amp;quot;1&amp;quot; style=&amp;quot;float: right; clear: right; margin: 0 0 1em 1em; border-collapse: collapse;&amp;quot;&lt;br /&gt;
! {{chembox header}} | {{PAGENAME}} &amp;lt;!-- replace if not identical with the article name --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; width=&amp;quot;300&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image:It-Dihydroartemisinin.jpg|thumb|]]&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | General&lt;br /&gt;
|-&lt;br /&gt;
| [[IUPAC nomenclature|Systematic name]]&lt;br /&gt;
|Dihydroartemisinin&lt;br /&gt;
|-&lt;br /&gt;
| Other names&lt;br /&gt;
|Dihydro-Qinghaosu&lt;br /&gt;
|-&lt;br /&gt;
| [[Chemical formula|Molecular formula]]&lt;br /&gt;
|C&amp;lt;sub&amp;gt;15&amp;lt;/sub&amp;gt;H&amp;lt;sub&amp;gt;24&amp;lt;/sub&amp;gt;O&amp;lt;sub&amp;gt;5&amp;lt;/sub&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
|-&lt;br /&gt;
| [[Molar mass]]&lt;br /&gt;
| 284.35 g/mol&lt;br /&gt;
|-&lt;br /&gt;
| Appearance&lt;br /&gt;
| White Crystalline Solid&lt;br /&gt;
|-&lt;br /&gt;
| [[CAS registry number|CAS number]]&lt;br /&gt;
| 81496-82-4&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Properties&lt;br /&gt;
|-&lt;br /&gt;
| [[Melting point]]&lt;br /&gt;
| 164-165°C (377-378 K)&lt;br /&gt;
|-&lt;br /&gt;
| Related compounds &lt;br /&gt;
| Sulfadoxine-pyrimethamine&lt;br /&gt;
|-&lt;br /&gt;
| {{chembox header}} | &amp;lt;small&amp;gt;Except where noted otherwise, data are given for&amp;lt;br /&amp;gt; materials in their [[standard state|standard state (at 25&amp;amp;nbsp;°C, 100&amp;amp;nbsp;kPa)]]&amp;lt;br /&amp;gt;[[wikipedia:Chemical infobox|Infobox disclaimer and references]]&amp;lt;/small&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
Dihydroartemisinin is produced by the reduction of &#039;&#039;&#039;Artemisinin&#039;&#039;&#039; (this reaction is covered later). Artemisinin is obtained from the &#039;&#039;Artemisia annua&#039;&#039; shrub which has long been used in traditional Chinese medicine. Not all shrubs of this species contain artemisinin. Apparently it is only produced when the plant is subjected to certain conditions. It can be synthesized from arteminisic acid.&lt;br /&gt;
&lt;br /&gt;
=== 3D Image ===&lt;br /&gt;
&amp;lt;jmol&amp;gt;&lt;br /&gt;
&amp;lt;jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;size&amp;gt;400&amp;lt;/size&amp;gt;&lt;br /&gt;
&amp;lt;color&amp;gt;orange&amp;lt;/color&amp;gt;&lt;br /&gt;
&amp;lt;script&amp;gt;zoom 150; 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;&lt;br /&gt;
HEADER    NONAME 07-Nov-06                                              NONE   1&lt;br /&gt;
TITLE                                                                   NONE   2&lt;br /&gt;
AUTHOR    WWW daemon apache                                             NONE   3&lt;br /&gt;
REVDAT   1  07-Nov-06     0                                             NONE   4&lt;br /&gt;
ATOM      1  C           0       3.741   1.404  -0.080  0.00  0.00           C+0&lt;br /&gt;
ATOM      2  C           0       2.459   0.577   0.026  0.00  0.00           C+0&lt;br /&gt;
ATOM      3  O           0       1.623   1.290   0.922  0.00  0.00           O+0&lt;br /&gt;
ATOM      4  C           0       2.876  -0.743   0.688  0.00  0.00           C+0&lt;br /&gt;
ATOM      5  C           0       1.913  -1.840   0.241  0.00  0.00           C+0&lt;br /&gt;
ATOM      6  C           0       0.490  -1.455   0.621  0.00  0.00           C+0&lt;br /&gt;
ATOM      7  H           0       0.473  -1.210   1.683  0.00  0.00           H+0&lt;br /&gt;
ATOM      8  C           0      -0.444  -2.641   0.388  0.00  0.00           C+0&lt;br /&gt;
ATOM      9  H           0      -0.007  -3.537   0.829  0.00  0.00           H+0&lt;br /&gt;
ATOM     10  C           0      -0.628  -2.854  -1.116  0.00  0.00           C+0&lt;br /&gt;
ATOM     11  C           0      -1.808  -2.373   1.029  0.00  0.00           C+0&lt;br /&gt;
ATOM     12  C           0      -2.169  -0.897   0.834  0.00  0.00           C+0&lt;br /&gt;
ATOM     13  C           0      -1.473  -0.395  -0.435  0.00  0.00           C+0&lt;br /&gt;
ATOM     14  H           0      -1.591  -1.151  -1.212  0.00  0.00           H+0&lt;br /&gt;
ATOM     15  C           0      -2.110   0.887  -0.919  0.00  0.00           C+0&lt;br /&gt;
ATOM     16  H           0      -1.896   1.007  -1.981  0.00  0.00           H+0&lt;br /&gt;
ATOM     17  C           0      -3.625   0.787  -0.730  0.00  0.00           C+0&lt;br /&gt;
ATOM     18  C           0      -1.607   2.112  -0.177  0.00  0.00           C+0&lt;br /&gt;
ATOM     19  H           0      -1.990   3.008  -0.666  0.00  0.00           H+0&lt;br /&gt;
ATOM     20  O           0      -2.084   2.074   1.169  0.00  0.00           O+0&lt;br /&gt;
ATOM     21  O           0      -0.189   2.160  -0.166  0.00  0.00           O+0&lt;br /&gt;
ATOM     22  C           0       0.261   1.066   0.602  0.00  0.00           C+0&lt;br /&gt;
ATOM     23  H           0      -0.310   1.039   1.530  0.00  0.00           H+0&lt;br /&gt;
ATOM     24  C           0       0.019  -0.241  -0.155  0.00  0.00           C+0&lt;br /&gt;
ATOM     25  O           0       0.728  -0.237  -1.400  0.00  0.00           O+0&lt;br /&gt;
ATOM     26  O           0       1.969   0.472  -1.272  0.00  0.00           O+0&lt;br /&gt;
ATOM     27  H           0       4.198   1.494   0.906  0.00  0.00           H+0&lt;br /&gt;
ATOM     28  H           0       4.436   0.912  -0.759  0.00  0.00           H+0&lt;br /&gt;
ATOM     29  H           0       3.502   2.397  -0.461  0.00  0.00           H+0&lt;br /&gt;
ATOM     30  H           0       3.891  -1.000   0.383  0.00  0.00           H+0&lt;br /&gt;
ATOM     31  H           0       2.833  -0.638   1.772  0.00  0.00           H+0&lt;br /&gt;
ATOM     32  H           0       1.980  -1.964  -0.840  0.00  0.00           H+0&lt;br /&gt;
ATOM     33  H           0       2.179  -2.778   0.731  0.00  0.00           H+0&lt;br /&gt;
ATOM     34  H           0       0.069  -3.618  -1.462  0.00  0.00           H+0&lt;br /&gt;
ATOM     35  H           0      -1.650  -3.176  -1.315  0.00  0.00           H+0&lt;br /&gt;
ATOM     36  H           0      -0.433  -1.919  -1.641  0.00  0.00           H+0&lt;br /&gt;
ATOM     37  H           0      -2.563  -3.000   0.555  0.00  0.00           H+0&lt;br /&gt;
ATOM     38  H           0      -1.761  -2.600   2.094  0.00  0.00           H+0&lt;br /&gt;
ATOM     39  H           0      -3.249  -0.795   0.726  0.00  0.00           H+0&lt;br /&gt;
ATOM     40  H           0      -1.829  -0.319   1.693  0.00  0.00           H+0&lt;br /&gt;
ATOM     41  H           0      -3.858   0.772   0.334  0.00  0.00           H+0&lt;br /&gt;
ATOM     42  H           0      -4.107   1.647  -1.196  0.00  0.00           H+0&lt;br /&gt;
ATOM     43  H           0      -3.989  -0.129  -1.195  0.00  0.00           H+0&lt;br /&gt;
ATOM     44  H           0      -1.746   2.866   1.608  0.00  0.00           H+0&lt;br /&gt;
CONECT    1    2   27   28   29                                         NONE  49&lt;br /&gt;
CONECT    2    1   26    3    4                                         NONE  50&lt;br /&gt;
CONECT    3    2   22    0    0                                         NONE  51&lt;br /&gt;
CONECT    4    2    5   30   31                                         NONE  52&lt;br /&gt;
CONECT    5    4    6   32   33                                         NONE  53&lt;br /&gt;
CONECT    6    5   24    7    8                                         NONE  54&lt;br /&gt;
CONECT    8    6    9   10   11                                         NONE  55&lt;br /&gt;
CONECT   10    8   34   35   36                                         NONE  56&lt;br /&gt;
CONECT   11    8   12   37   38                                         NONE  57&lt;br /&gt;
CONECT   12   11   13   39   40                                         NONE  58&lt;br /&gt;
CONECT   13   12   24   14   15                                         NONE  59&lt;br /&gt;
CONECT   15   13   16   17   18                                         NONE  60&lt;br /&gt;
CONECT   17   15   41   42   43                                         NONE  61&lt;br /&gt;
CONECT   18   15   19   20   21                                         NONE  62&lt;br /&gt;
CONECT   20   18   44    0    0                                         NONE  63&lt;br /&gt;
CONECT   21   18   22    0    0                                         NONE  64&lt;br /&gt;
CONECT   22   21    3   23   24                                         NONE  65&lt;br /&gt;
CONECT   24   22   13    6   25                                         NONE  66&lt;br /&gt;
CONECT   25   24   26    0    0                                         NONE  67&lt;br /&gt;
CONECT   26   25    2    0    0                                         NONE  68&lt;br /&gt;
END                                                                     NONE  69&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;
&lt;br /&gt;
=== H&amp;lt;sup&amp;gt;1&amp;lt;/sup&amp;gt; NMR Spectrum ===&lt;br /&gt;
[[Image:dihydroartemisinin H1 nmr.bmp]]&lt;br /&gt;
&lt;br /&gt;
== Synthesis ==&lt;br /&gt;
&lt;br /&gt;
The image below shows the synthesis of Dihydroartemisinin from Artemisinin using NaBH&amp;lt;sub&amp;gt;4&amp;lt;/sub&amp;gt;:&lt;br /&gt;
&lt;br /&gt;
[[Image:formation.jpg]]&lt;br /&gt;
==So how does it actually work?==&lt;br /&gt;
&lt;br /&gt;
Although the specific reaction mechanism is not well understood it is known how the malarial parasite is killed. The parasite attacks red blood cells and consumes haemoglobin and producing heme (an iron-based complex). The iron in heme reacts with the peroxide on the &#039;&#039;&#039;Dihydroartemisinin&#039;&#039;&#039; generating high-valent iron-oxo species. Further reactions occur that produce reactive oxygen radicals which damage the parasite leading to its death.&lt;br /&gt;
&lt;br /&gt;
[[Image:heme.gif]]-&amp;gt;Heme&lt;br /&gt;
&lt;br /&gt;
== References &amp;amp; Useful Links ==&lt;br /&gt;
&lt;br /&gt;
http://www.buyreagents.com/dihydroartemisinin.html &lt;br /&gt;
&lt;br /&gt;
http://en.wikipedia.org/wiki/Artemisinin&lt;br /&gt;
&lt;br /&gt;
Synthesis Diagram: &#039;&#039;&#039;Immunodetection of Artemisinin in Artemisia Annua Cultivated in Hydroponic Conditions&#039;&#039;&#039;; Journal; Jaziri, Mondher; Diallo, Billo; Vanhaelen, Maurice; Homes, Jacques; Yoshimatsu, Kayo; Shimomura, Koichiro; PYTCAS; Phytochemistry; EN; 33; 4; 1993; 821-826&lt;br /&gt;
&lt;br /&gt;
http://en.wikipedia.org/wiki/Artemisinin#_ref-2&lt;/div&gt;</summary>
		<author><name>Rw305</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It:MSG&amp;diff=5435</id>
		<title>It:MSG</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It:MSG&amp;diff=5435"/>
		<updated>2006-11-16T11:56:26Z</updated>

		<summary type="html">&lt;p&gt;Rw305: /* Abstrac */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;==Abstract==&lt;br /&gt;
&#039;&#039;&#039;Monosodium Glutamate&#039;&#039;&#039; is more commonly known as &#039;&#039;&#039;MSG&#039;&#039;&#039; and has become the choice chemical for the enhancement of flavour in many foods. It was originally discovered in 1909 by the Ajinomoto Corporation in Japan.&lt;br /&gt;
&lt;br /&gt;
==The Basics==&lt;/div&gt;</summary>
		<author><name>Rw305</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It:MSG&amp;diff=5434</id>
		<title>It:MSG</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It:MSG&amp;diff=5434"/>
		<updated>2006-11-16T11:56:04Z</updated>

		<summary type="html">&lt;p&gt;Rw305: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;==Abstrac==&lt;br /&gt;
&#039;&#039;&#039;Monosodium Glutamate&#039;&#039;&#039; is more commonly known as &#039;&#039;&#039;MSG&#039;&#039;&#039; and has become the choice chemical for the enhancement of flavour in many foods. It was originally discovered in 1909 by the Ajinomoto Corporation in Japan.&lt;br /&gt;
&lt;br /&gt;
==The Basics==&lt;/div&gt;</summary>
		<author><name>Rw305</name></author>
	</entry>
</feed>