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	<title>LBGTGccc:16000SC01:18000SC01:16000SC01 2 - Revision history</title>
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	<updated>2026-05-01T09:06:26Z</updated>
	<subtitle>Revision history for this page on the wiki</subtitle>
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	<entry>
		<id>https://lipidbank.jp/mediawiki/index.php?title=LBGTGccc:16000SC01:18000SC01:16000SC01_2&amp;diff=68536&amp;oldid=prev</id>
		<title>Editor: LBGTGccc:16000SC01:18000SC01:16000SC01:02 moved to LBGTGccc:16000SC01:18000SC01:16000SC01 2</title>
		<link rel="alternate" type="text/html" href="https://lipidbank.jp/mediawiki/index.php?title=LBGTGccc:16000SC01:18000SC01:16000SC01_2&amp;diff=68536&amp;oldid=prev"/>
		<updated>2010-04-14T21:00:00Z</updated>

		<summary type="html">&lt;p&gt;&lt;a href=&quot;/wiki/LBGTGccc:16000SC01:18000SC01:16000SC01:02&quot; class=&quot;mw-redirect&quot; title=&quot;LBGTGccc:16000SC01:18000SC01:16000SC01:02&quot;&gt;LBGTGccc:16000SC01:18000SC01:16000SC01:02&lt;/a&gt; moved to &lt;a href=&quot;/wiki/LBGTGccc:16000SC01:18000SC01:16000SC01_2&quot; title=&quot;LBGTGccc:16000SC01:18000SC01:16000SC01 2&quot;&gt;LBGTGccc:16000SC01:18000SC01:16000SC01 2&lt;/a&gt;&lt;/p&gt;
&lt;table style=&quot;background-color: #fff; color: #202122;&quot; data-mw=&quot;interface&quot;&gt;
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				&lt;td colspan=&quot;2&quot; style=&quot;background-color: #fff; color: #202122; text-align: center;&quot;&gt;← Older revision&lt;/td&gt;
				&lt;td colspan=&quot;2&quot; style=&quot;background-color: #fff; color: #202122; text-align: center;&quot;&gt;Revision as of 06:00, 15 April 2010&lt;/td&gt;
				&lt;/tr&gt;&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot; id=&quot;mw-diff-left-l4&quot;&gt;Line 4:&lt;/td&gt;
&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot;&gt;Line 4:&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;|LipidBank=NAG5156&lt;/div&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;|LipidBank=NAG5156&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;|SysName=Glycerol 1,3-dihexadecanoate 2- (9-octadecenoate)  (Z) -form&lt;/div&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;|SysName=Glycerol 1,3-dihexadecanoate 2- (9-octadecenoate)  (Z) -form&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;−&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;|Common Name=&amp;amp;&amp;amp;alpha,alpha-Dipalmitoolein&amp;amp;&amp;amp;2-Oleodipalmitin&amp;amp;&amp;amp;9-Octadecenoic acid 2- [  (1-oxohexadecyl)  oxy ] -1- [   [  (1-oxohexadecyl) oxy ]  methyl ]  ethyl ester&lt;del style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;&amp;amp;&amp;amp;Glycerol 1,3-dihexadecanoate 2- (9-octadecenoate)  (Z) -form&lt;/del&gt;&amp;amp;&amp;amp;&lt;/div&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;|Common Name=&amp;amp;&amp;amp;alpha,alpha-Dipalmitoolein&amp;amp;&amp;amp;2-Oleodipalmitin&amp;amp;&amp;amp;9-Octadecenoic acid 2- [  (1-oxohexadecyl)  oxy ] -1- [   [  (1-oxohexadecyl) oxy ]  methyl ]  ethyl ester&amp;amp;&amp;amp;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;|Melting Point=Cryst.(acetone). Mp 37.2°C. Exhibits polymorphism.  beta 1=36.7°C. &amp;lt;&amp;lt;5144&amp;gt;&amp;gt;The crystal shows the typical polymorphism phenomenon. Knowledge and naming on got polymorphism are different by the researcher, and there is following correspondence on got polymolphism each. The crystallization phenomenon of the POP is greatly dependent on the polymorphism. By being dependent on the temperature of the crystallization, got polymorphism and the crystallization kinetic change.&lt;/div&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;|Melting Point=Cryst.(acetone). Mp 37.2°C. Exhibits polymorphism.  beta 1=36.7°C. &amp;lt;&amp;lt;5144&amp;gt;&amp;gt;The crystal shows the typical polymorphism phenomenon. Knowledge and naming on got polymorphism are different by the researcher, and there is following correspondence on got polymolphism each. The crystallization phenomenon of the POP is greatly dependent on the polymorphism. By being dependent on the temperature of the crystallization, got polymorphism and the crystallization kinetic change.&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;|Solubility= 1.65 at 13.9°C, 1.30 at 13.6°C, 1.05 at 12.9°C, 0.80 at 11.5°C g solute/100g solvent in tetradecane&amp;lt;&amp;lt;5182&amp;gt;&amp;gt;&lt;/div&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;|Solubility= 1.65 at 13.9°C, 1.30 at 13.6°C, 1.05 at 12.9°C, 0.80 at 11.5°C g solute/100g solvent in tetradecane&amp;lt;&amp;lt;5182&amp;gt;&amp;gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;

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&lt;/table&gt;</summary>
		<author><name>Editor</name></author>
	</entry>
	<entry>
		<id>https://lipidbank.jp/mediawiki/index.php?title=LBGTGccc:16000SC01:18000SC01:16000SC01_2&amp;diff=68535&amp;oldid=prev</id>
		<title>Editor: LBGTGccc:16000SC01:18000SC01:16000SC01:02 moved to LBGTGccc:16000SC01:18000SC01:16000SC01 2</title>
		<link rel="alternate" type="text/html" href="https://lipidbank.jp/mediawiki/index.php?title=LBGTGccc:16000SC01:18000SC01:16000SC01_2&amp;diff=68535&amp;oldid=prev"/>
		<updated>2010-02-25T10:00:10Z</updated>

		<summary type="html">&lt;p&gt;&lt;a href=&quot;/wiki/LBGTGccc:16000SC01:18000SC01:16000SC01:02&quot; class=&quot;mw-redirect&quot; title=&quot;LBGTGccc:16000SC01:18000SC01:16000SC01:02&quot;&gt;LBGTGccc:16000SC01:18000SC01:16000SC01:02&lt;/a&gt; moved to &lt;a href=&quot;/wiki/LBGTGccc:16000SC01:18000SC01:16000SC01_2&quot; title=&quot;LBGTGccc:16000SC01:18000SC01:16000SC01 2&quot;&gt;LBGTGccc:16000SC01:18000SC01:16000SC01 2&lt;/a&gt;&lt;/p&gt;
&lt;table style=&quot;background-color: #fff; color: #202122;&quot; data-mw=&quot;interface&quot;&gt;
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				&lt;td colspan=&quot;1&quot; style=&quot;background-color: #fff; color: #202122; text-align: center;&quot;&gt;← Older revision&lt;/td&gt;
				&lt;td colspan=&quot;1&quot; style=&quot;background-color: #fff; color: #202122; text-align: center;&quot;&gt;Revision as of 19:00, 25 February 2010&lt;/td&gt;
				&lt;/tr&gt;&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-notice&quot; lang=&quot;en&quot;&gt;&lt;div class=&quot;mw-diff-empty&quot;&gt;(No difference)&lt;/div&gt;
&lt;/td&gt;&lt;/tr&gt;&lt;/table&gt;</summary>
		<author><name>Editor</name></author>
	</entry>
	<entry>
		<id>https://lipidbank.jp/mediawiki/index.php?title=LBGTGccc:16000SC01:18000SC01:16000SC01_2&amp;diff=68534&amp;oldid=prev</id>
		<title>Editor: LBGTGccc:16000SC01:18000SC01:16000SC01:02 moved to LBGTGccc:16000SC01:18000SC01:16000SC01 2</title>
		<link rel="alternate" type="text/html" href="https://lipidbank.jp/mediawiki/index.php?title=LBGTGccc:16000SC01:18000SC01:16000SC01_2&amp;diff=68534&amp;oldid=prev"/>
		<updated>2010-02-19T14:00:10Z</updated>

		<summary type="html">&lt;p&gt;&lt;a href=&quot;/wiki/LBGTGccc:16000SC01:18000SC01:16000SC01:02&quot; class=&quot;mw-redirect&quot; title=&quot;LBGTGccc:16000SC01:18000SC01:16000SC01:02&quot;&gt;LBGTGccc:16000SC01:18000SC01:16000SC01:02&lt;/a&gt; moved to &lt;a href=&quot;/wiki/LBGTGccc:16000SC01:18000SC01:16000SC01_2&quot; title=&quot;LBGTGccc:16000SC01:18000SC01:16000SC01 2&quot;&gt;LBGTGccc:16000SC01:18000SC01:16000SC01 2&lt;/a&gt;&lt;/p&gt;
&lt;table style=&quot;background-color: #fff; color: #202122;&quot; data-mw=&quot;interface&quot;&gt;
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				&lt;td colspan=&quot;2&quot; style=&quot;background-color: #fff; color: #202122; text-align: center;&quot;&gt;← Older revision&lt;/td&gt;
				&lt;td colspan=&quot;2&quot; style=&quot;background-color: #fff; color: #202122; text-align: center;&quot;&gt;Revision as of 23:00, 19 February 2010&lt;/td&gt;
				&lt;/tr&gt;&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot; id=&quot;mw-diff-left-l5&quot;&gt;Line 5:&lt;/td&gt;
&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot;&gt;Line 5:&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;|SysName=Glycerol 1,3-dihexadecanoate 2- (9-octadecenoate)  (Z) -form&lt;/div&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;|SysName=Glycerol 1,3-dihexadecanoate 2- (9-octadecenoate)  (Z) -form&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;|Common Name=&amp;amp;&amp;amp;alpha,alpha-Dipalmitoolein&amp;amp;&amp;amp;2-Oleodipalmitin&amp;amp;&amp;amp;9-Octadecenoic acid 2- [  (1-oxohexadecyl)  oxy ] -1- [   [  (1-oxohexadecyl) oxy ]  methyl ]  ethyl ester&amp;amp;&amp;amp;Glycerol 1,3-dihexadecanoate 2- (9-octadecenoate)  (Z) -form&amp;amp;&amp;amp;&lt;/div&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;|Common Name=&amp;amp;&amp;amp;alpha,alpha-Dipalmitoolein&amp;amp;&amp;amp;2-Oleodipalmitin&amp;amp;&amp;amp;9-Octadecenoic acid 2- [  (1-oxohexadecyl)  oxy ] -1- [   [  (1-oxohexadecyl) oxy ]  methyl ]  ethyl ester&amp;amp;&amp;amp;Glycerol 1,3-dihexadecanoate 2- (9-octadecenoate)  (Z) -form&amp;amp;&amp;amp;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;−&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;|Melting Point=Cryst.(acetone). Mp 37.2°C. Exhibits polymorphism. &lt;del style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;beta1&lt;/del&gt;=36.7°C. &amp;lt;&amp;lt;5144&amp;gt;&amp;gt;The crystal shows the typical polymorphism phenomenon. Knowledge and naming on got polymorphism are different by the researcher, and there is following correspondence on got polymolphism each. The crystallization phenomenon of the POP is greatly dependent on the polymorphism. By being dependent on the temperature of the crystallization, got polymorphism and the crystallization kinetic change.&lt;/div&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;|Melting Point=Cryst.(acetone). Mp 37.2°C. Exhibits polymorphism. &lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt; beta 1&lt;/ins&gt;=36.7°C. &amp;lt;&amp;lt;5144&amp;gt;&amp;gt;The crystal shows the typical polymorphism phenomenon. Knowledge and naming on got polymorphism are different by the researcher, and there is following correspondence on got polymolphism each. The crystallization phenomenon of the POP is greatly dependent on the polymorphism. By being dependent on the temperature of the crystallization, got polymorphism and the crystallization kinetic change.&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;|Solubility= 1.65 at 13.9°C, 1.30 at 13.6°C, 1.05 at 12.9°C, 0.80 at 11.5°C g solute/100g solvent in tetradecane&amp;lt;&amp;lt;5182&amp;gt;&amp;gt;&lt;/div&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;|Solubility= 1.65 at 13.9°C, 1.30 at 13.6°C, 1.05 at 12.9°C, 0.80 at 11.5°C g solute/100g solvent in tetradecane&amp;lt;&amp;lt;5182&amp;gt;&amp;gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;|NMR Spectra=13C-NMR spectra &amp;lt;&amp;lt;5183&amp;gt;&amp;gt;,  &lt;/div&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;|NMR Spectra=13C-NMR spectra &amp;lt;&amp;lt;5183&amp;gt;&amp;gt;,  &lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;/table&gt;</summary>
		<author><name>Editor</name></author>
	</entry>
	<entry>
		<id>https://lipidbank.jp/mediawiki/index.php?title=LBGTGccc:16000SC01:18000SC01:16000SC01_2&amp;diff=68533&amp;oldid=prev</id>
		<title>Editor: LBGTGccc:16000SC01:18000SC01:16000SC01:02 moved to LBGTGccc:16000SC01:18000SC01:16000SC01 2</title>
		<link rel="alternate" type="text/html" href="https://lipidbank.jp/mediawiki/index.php?title=LBGTGccc:16000SC01:18000SC01:16000SC01_2&amp;diff=68533&amp;oldid=prev"/>
		<updated>2010-02-19T14:00:00Z</updated>

		<summary type="html">&lt;p&gt;&lt;a href=&quot;/wiki/LBGTGccc:16000SC01:18000SC01:16000SC01:02&quot; class=&quot;mw-redirect&quot; title=&quot;LBGTGccc:16000SC01:18000SC01:16000SC01:02&quot;&gt;LBGTGccc:16000SC01:18000SC01:16000SC01:02&lt;/a&gt; moved to &lt;a href=&quot;/wiki/LBGTGccc:16000SC01:18000SC01:16000SC01_2&quot; title=&quot;LBGTGccc:16000SC01:18000SC01:16000SC01 2&quot;&gt;LBGTGccc:16000SC01:18000SC01:16000SC01 2&lt;/a&gt;&lt;/p&gt;
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				&lt;td colspan=&quot;2&quot; style=&quot;background-color: #fff; color: #202122; text-align: center;&quot;&gt;← Older revision&lt;/td&gt;
				&lt;td colspan=&quot;2&quot; style=&quot;background-color: #fff; color: #202122; text-align: center;&quot;&gt;Revision as of 23:00, 19 February 2010&lt;/td&gt;
				&lt;/tr&gt;&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot; id=&quot;mw-diff-left-l5&quot;&gt;Line 5:&lt;/td&gt;
&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot;&gt;Line 5:&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;|SysName=Glycerol 1,3-dihexadecanoate 2- (9-octadecenoate)  (Z) -form&lt;/div&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;|SysName=Glycerol 1,3-dihexadecanoate 2- (9-octadecenoate)  (Z) -form&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;|Common Name=&amp;amp;&amp;amp;alpha,alpha-Dipalmitoolein&amp;amp;&amp;amp;2-Oleodipalmitin&amp;amp;&amp;amp;9-Octadecenoic acid 2- [  (1-oxohexadecyl)  oxy ] -1- [   [  (1-oxohexadecyl) oxy ]  methyl ]  ethyl ester&amp;amp;&amp;amp;Glycerol 1,3-dihexadecanoate 2- (9-octadecenoate)  (Z) -form&amp;amp;&amp;amp;&lt;/div&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;|Common Name=&amp;amp;&amp;amp;alpha,alpha-Dipalmitoolein&amp;amp;&amp;amp;2-Oleodipalmitin&amp;amp;&amp;amp;9-Octadecenoic acid 2- [  (1-oxohexadecyl)  oxy ] -1- [   [  (1-oxohexadecyl) oxy ]  methyl ]  ethyl ester&amp;amp;&amp;amp;Glycerol 1,3-dihexadecanoate 2- (9-octadecenoate)  (Z) -form&amp;amp;&amp;amp;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;−&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;|Melting Point=Cryst.(acetone). Mp 37.2°C. Exhibits polymorphism. &lt;del style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;&amp;lt;FONT FACE=&quot;Symbol&quot;&amp;gt;b&amp;lt;/FONT&amp;gt;1&lt;/del&gt;=36.7°C. &amp;lt;&amp;lt;5144&amp;gt;&amp;gt;The crystal shows the typical polymorphism phenomenon. Knowledge and naming on got polymorphism are different by the researcher, and there is following correspondence on got polymolphism each. The crystallization phenomenon of the POP is greatly dependent on the polymorphism. By being dependent on the temperature of the crystallization, got polymorphism and the crystallization kinetic change.&lt;/div&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;|Melting Point=Cryst.(acetone). Mp 37.2°C. Exhibits polymorphism. &lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;beta1&lt;/ins&gt;=36.7°C. &amp;lt;&amp;lt;5144&amp;gt;&amp;gt;The crystal shows the typical polymorphism phenomenon. Knowledge and naming on got polymorphism are different by the researcher, and there is following correspondence on got polymolphism each. The crystallization phenomenon of the POP is greatly dependent on the polymorphism. By being dependent on the temperature of the crystallization, got polymorphism and the crystallization kinetic change.&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;|Solubility= 1.65 at 13.9°C, 1.30 at 13.6°C, 1.05 at 12.9°C, 0.80 at 11.5°C g solute/100g solvent in tetradecane&amp;lt;&amp;lt;5182&amp;gt;&amp;gt;&lt;/div&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;|Solubility= 1.65 at 13.9°C, 1.30 at 13.6°C, 1.05 at 12.9°C, 0.80 at 11.5°C g solute/100g solvent in tetradecane&amp;lt;&amp;lt;5182&amp;gt;&amp;gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;|NMR Spectra=13C-NMR spectra &amp;lt;&amp;lt;5183&amp;gt;&amp;gt;,  &lt;/div&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;|NMR Spectra=13C-NMR spectra &amp;lt;&amp;lt;5183&amp;gt;&amp;gt;,  &lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;/table&gt;</summary>
		<author><name>Editor</name></author>
	</entry>
	<entry>
		<id>https://lipidbank.jp/mediawiki/index.php?title=LBGTGccc:16000SC01:18000SC01:16000SC01_2&amp;diff=68532&amp;oldid=prev</id>
		<title>Editor: LBGTGccc:16000SC01:18000SC01:16000SC01:02 moved to LBGTGccc:16000SC01:18000SC01:16000SC01 2</title>
		<link rel="alternate" type="text/html" href="https://lipidbank.jp/mediawiki/index.php?title=LBGTGccc:16000SC01:18000SC01:16000SC01_2&amp;diff=68532&amp;oldid=prev"/>
		<updated>2010-02-18T15:00:00Z</updated>

		<summary type="html">&lt;p&gt;&lt;a href=&quot;/wiki/LBGTGccc:16000SC01:18000SC01:16000SC01:02&quot; class=&quot;mw-redirect&quot; title=&quot;LBGTGccc:16000SC01:18000SC01:16000SC01:02&quot;&gt;LBGTGccc:16000SC01:18000SC01:16000SC01:02&lt;/a&gt; moved to &lt;a href=&quot;/wiki/LBGTGccc:16000SC01:18000SC01:16000SC01_2&quot; title=&quot;LBGTGccc:16000SC01:18000SC01:16000SC01 2&quot;&gt;LBGTGccc:16000SC01:18000SC01:16000SC01 2&lt;/a&gt;&lt;/p&gt;
&lt;table style=&quot;background-color: #fff; color: #202122;&quot; data-mw=&quot;interface&quot;&gt;
				&lt;col class=&quot;diff-marker&quot; /&gt;
				&lt;col class=&quot;diff-content&quot; /&gt;
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				&lt;td colspan=&quot;2&quot; style=&quot;background-color: #fff; color: #202122; text-align: center;&quot;&gt;← Older revision&lt;/td&gt;
				&lt;td colspan=&quot;2&quot; style=&quot;background-color: #fff; color: #202122; text-align: center;&quot;&gt;Revision as of 00:00, 19 February 2010&lt;/td&gt;
				&lt;/tr&gt;&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot; id=&quot;mw-diff-left-l4&quot;&gt;Line 4:&lt;/td&gt;
&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot;&gt;Line 4:&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;|LipidBank=NAG5156&lt;/div&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;|LipidBank=NAG5156&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;|SysName=Glycerol 1,3-dihexadecanoate 2- (9-octadecenoate)  (Z) -form&lt;/div&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;|SysName=Glycerol 1,3-dihexadecanoate 2- (9-octadecenoate)  (Z) -form&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;−&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;|Common Name=alpha,alpha-&lt;del style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;Dipalmitoolein2&lt;/del&gt;-&lt;del style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;Oleodipalmitin9&lt;/del&gt;-Octadecenoic acid 2- [  (1-oxohexadecyl)  oxy ] -1- [   [  (1-oxohexadecyl) oxy ]  methyl ]  ethyl &lt;del style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;esterGlycerol &lt;/del&gt;1,3-dihexadecanoate 2- (9-octadecenoate)  (Z) -form&lt;/div&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;|Common Name=&lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;&amp;amp;&amp;amp;&lt;/ins&gt;alpha,alpha-&lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;Dipalmitoolein&amp;amp;&amp;amp;2&lt;/ins&gt;-&lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;Oleodipalmitin&amp;amp;&amp;amp;9&lt;/ins&gt;-Octadecenoic acid 2- [  (1-oxohexadecyl)  oxy ] -1- [   [  (1-oxohexadecyl) oxy ]  methyl ]  ethyl &lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;ester&amp;amp;&amp;amp;Glycerol &lt;/ins&gt;1,3-dihexadecanoate 2- (9-octadecenoate)  (Z) -form&lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;&amp;amp;&amp;amp;&lt;/ins&gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;−&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;|Melting Point=Cryst.(acetone). Mp 37.2°C. Exhibits polymorphism. FONT FACE=&lt;del style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;Symbolb&lt;/del&gt;/&lt;del style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;FONT1&lt;/del&gt;=36.7°C. &lt;del style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;5144The &lt;/del&gt;crystal shows the typical polymorphism phenomenon. Knowledge and naming on got polymorphism are different by the researcher, and there is following correspondence on got polymolphism each. The crystallization phenomenon of the POP is greatly dependent on the polymorphism. By being dependent on the temperature of the crystallization, got polymorphism and the crystallization kinetic change.&lt;/div&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;|Melting Point=Cryst.(acetone). Mp 37.2°C. Exhibits polymorphism. &lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;&amp;lt;&lt;/ins&gt;FONT FACE=&lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;&quot;Symbol&quot;&amp;gt;b&amp;lt;&lt;/ins&gt;/&lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;FONT&amp;gt;1&lt;/ins&gt;=36.7°C. &lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;&amp;lt;&amp;lt;5144&amp;gt;&amp;gt;The &lt;/ins&gt;crystal shows the typical polymorphism phenomenon. Knowledge and naming on got polymorphism are different by the researcher, and there is following correspondence on got polymolphism each. The crystallization phenomenon of the POP is greatly dependent on the polymorphism. By being dependent on the temperature of the crystallization, got polymorphism and the crystallization kinetic change.&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;−&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;|Solubility= 1.65 at 13.9°C, 1.30 at 13.6°C, 1.05 at 12.9°C, 0.80 at 11.5°C g solute/100g solvent in &lt;del style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;tetradecane5182&lt;/del&gt;&lt;/div&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;|Solubility= 1.65 at 13.9°C, 1.30 at 13.6°C, 1.05 at 12.9°C, 0.80 at 11.5°C g solute/100g solvent in &lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;tetradecane&amp;lt;&amp;lt;5182&amp;gt;&amp;gt;&lt;/ins&gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;−&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;|NMR Spectra=13C-NMR spectra 5183,  &lt;/div&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;|NMR Spectra=13C-NMR spectra &lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;&amp;lt;&amp;lt;&lt;/ins&gt;5183&lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;&amp;gt;&amp;gt;&lt;/ins&gt;,  &lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;−&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;|NOTE Spectra=X-ray short spacing and long spacing 5184,  &lt;/div&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;|NOTE Spectra=X-ray short spacing and long spacing &lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;&amp;lt;&amp;lt;&lt;/ins&gt;5184&lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;&amp;gt;&amp;gt;&lt;/ins&gt;,  &lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;}}&lt;/div&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;}}&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;br&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;br&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;{{Lipid/Footer}}&lt;/div&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;{{Lipid/Footer}}&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;/table&gt;</summary>
		<author><name>Editor</name></author>
	</entry>
	<entry>
		<id>https://lipidbank.jp/mediawiki/index.php?title=LBGTGccc:16000SC01:18000SC01:16000SC01_2&amp;diff=68531&amp;oldid=prev</id>
		<title>Editor: LBGTGccc:16000SC01:18000SC01:16000SC01:02 moved to LBGTGccc:16000SC01:18000SC01:16000SC01 2</title>
		<link rel="alternate" type="text/html" href="https://lipidbank.jp/mediawiki/index.php?title=LBGTGccc:16000SC01:18000SC01:16000SC01_2&amp;diff=68531&amp;oldid=prev"/>
		<updated>2010-01-27T20:00:00Z</updated>

		<summary type="html">&lt;p&gt;&lt;a href=&quot;/wiki/LBGTGccc:16000SC01:18000SC01:16000SC01:02&quot; class=&quot;mw-redirect&quot; title=&quot;LBGTGccc:16000SC01:18000SC01:16000SC01:02&quot;&gt;LBGTGccc:16000SC01:18000SC01:16000SC01:02&lt;/a&gt; moved to &lt;a href=&quot;/wiki/LBGTGccc:16000SC01:18000SC01:16000SC01_2&quot; title=&quot;LBGTGccc:16000SC01:18000SC01:16000SC01 2&quot;&gt;LBGTGccc:16000SC01:18000SC01:16000SC01 2&lt;/a&gt;&lt;/p&gt;
&lt;table style=&quot;background-color: #fff; color: #202122;&quot; data-mw=&quot;interface&quot;&gt;
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				&lt;td colspan=&quot;2&quot; style=&quot;background-color: #fff; color: #202122; text-align: center;&quot;&gt;← Older revision&lt;/td&gt;
				&lt;td colspan=&quot;2&quot; style=&quot;background-color: #fff; color: #202122; text-align: center;&quot;&gt;Revision as of 05:00, 28 January 2010&lt;/td&gt;
				&lt;/tr&gt;&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot; id=&quot;mw-diff-left-l4&quot;&gt;Line 4:&lt;/td&gt;
&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot;&gt;Line 4:&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;|LipidBank=NAG5156&lt;/div&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;|LipidBank=NAG5156&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;|SysName=Glycerol 1,3-dihexadecanoate 2- (9-octadecenoate)  (Z) -form&lt;/div&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;|SysName=Glycerol 1,3-dihexadecanoate 2- (9-octadecenoate)  (Z) -form&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;−&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;|Common Name=&lt;del style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;&amp;amp;&amp;amp;&lt;/del&gt;alpha,alpha-&lt;del style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;Dipalmitoolein&amp;amp;&amp;amp;2&lt;/del&gt;-&lt;del style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;Oleodipalmitin&amp;amp;&amp;amp;9&lt;/del&gt;-Octadecenoic acid 2- [  (1-oxohexadecyl)  oxy ] -1- [   [  (1-oxohexadecyl) oxy ]  methyl ]  ethyl &lt;del style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;ester&amp;amp;&amp;amp;Glycerol &lt;/del&gt;1,3-dihexadecanoate 2- (9-octadecenoate)  (Z) -form&lt;del style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;&amp;amp;&amp;amp;&lt;/del&gt;&lt;/div&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;|Common Name=alpha,alpha-&lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;Dipalmitoolein2&lt;/ins&gt;-&lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;Oleodipalmitin9&lt;/ins&gt;-Octadecenoic acid 2- [  (1-oxohexadecyl)  oxy ] -1- [   [  (1-oxohexadecyl) oxy ]  methyl ]  ethyl &lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;esterGlycerol &lt;/ins&gt;1,3-dihexadecanoate 2- (9-octadecenoate)  (Z) -form&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;−&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;|Melting Point=Cryst.(acetone). Mp 37.2°C. Exhibits polymorphism. &lt;del style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;&amp;lt;&lt;/del&gt;FONT FACE=&lt;del style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;&quot;Symbol&quot;&amp;gt;b&amp;lt;&lt;/del&gt;/&lt;del style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;FONT&amp;gt;1&lt;/del&gt;=36.7°C. &lt;del style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;&amp;lt;&amp;lt;5144&amp;gt;&amp;gt;The &lt;/del&gt;crystal shows the typical polymorphism phenomenon. Knowledge and naming on got polymorphism are different by the researcher, and there is following correspondence on got polymolphism each. The crystallization phenomenon of the POP is greatly dependent on the polymorphism. By being dependent on the temperature of the crystallization, got polymorphism and the crystallization kinetic change.&lt;/div&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;|Melting Point=Cryst.(acetone). Mp 37.2°C. Exhibits polymorphism. FONT FACE=&lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;Symbolb&lt;/ins&gt;/&lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;FONT1&lt;/ins&gt;=36.7°C. &lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;5144The &lt;/ins&gt;crystal shows the typical polymorphism phenomenon. Knowledge and naming on got polymorphism are different by the researcher, and there is following correspondence on got polymolphism each. The crystallization phenomenon of the POP is greatly dependent on the polymorphism. By being dependent on the temperature of the crystallization, got polymorphism and the crystallization kinetic change.&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;−&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;|Solubility= 1.65 at 13.9°C, 1.30 at 13.6°C, 1.05 at 12.9°C, 0.80 at 11.5°C g solute/100g solvent in &lt;del style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;tetradecane&amp;lt;&amp;lt;5182&amp;gt;&amp;gt;&lt;/del&gt;&lt;/div&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;|Solubility= 1.65 at 13.9°C, 1.30 at 13.6°C, 1.05 at 12.9°C, 0.80 at 11.5°C g solute/100g solvent in &lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;tetradecane5182&lt;/ins&gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;−&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;|NMR Spectra=13C-NMR spectra &lt;del style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;&amp;lt;&amp;lt;&lt;/del&gt;5183&lt;del style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;&amp;gt;&amp;gt;&lt;/del&gt;,  &lt;/div&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;|NMR Spectra=13C-NMR spectra 5183,  &lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;−&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;|NOTE Spectra=X-ray short spacing and long spacing &lt;del style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;&amp;lt;&amp;lt;&lt;/del&gt;5184&lt;del style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;&amp;gt;&amp;gt;&lt;/del&gt;,  &lt;/div&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;|NOTE Spectra=X-ray short spacing and long spacing 5184,  &lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;}}&lt;/div&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;}}&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;br&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;br&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;{{Lipid/Footer}}&lt;/div&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;{{Lipid/Footer}}&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;/table&gt;</summary>
		<author><name>Editor</name></author>
	</entry>
	<entry>
		<id>https://lipidbank.jp/mediawiki/index.php?title=LBGTGccc:16000SC01:18000SC01:16000SC01_2&amp;diff=68530&amp;oldid=prev</id>
		<title>Editor: LBGTGccc:16000SC01:18000SC01:16000SC01:02 moved to LBGTGccc:16000SC01:18000SC01:16000SC01 2</title>
		<link rel="alternate" type="text/html" href="https://lipidbank.jp/mediawiki/index.php?title=LBGTGccc:16000SC01:18000SC01:16000SC01_2&amp;diff=68530&amp;oldid=prev"/>
		<updated>2010-01-20T01:39:18Z</updated>

		<summary type="html">&lt;p&gt;&lt;a href=&quot;/wiki/LBGTGccc:16000SC01:18000SC01:16000SC01:02&quot; class=&quot;mw-redirect&quot; title=&quot;LBGTGccc:16000SC01:18000SC01:16000SC01:02&quot;&gt;LBGTGccc:16000SC01:18000SC01:16000SC01:02&lt;/a&gt; moved to &lt;a href=&quot;/wiki/LBGTGccc:16000SC01:18000SC01:16000SC01_2&quot; title=&quot;LBGTGccc:16000SC01:18000SC01:16000SC01 2&quot;&gt;LBGTGccc:16000SC01:18000SC01:16000SC01 2&lt;/a&gt;&lt;/p&gt;
&lt;table style=&quot;background-color: #fff; color: #202122;&quot; data-mw=&quot;interface&quot;&gt;
				&lt;tr class=&quot;diff-title&quot; lang=&quot;en&quot;&gt;
				&lt;td colspan=&quot;1&quot; style=&quot;background-color: #fff; color: #202122; text-align: center;&quot;&gt;← Older revision&lt;/td&gt;
				&lt;td colspan=&quot;1&quot; style=&quot;background-color: #fff; color: #202122; text-align: center;&quot;&gt;Revision as of 10:39, 20 January 2010&lt;/td&gt;
				&lt;/tr&gt;&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-notice&quot; lang=&quot;en&quot;&gt;&lt;div class=&quot;mw-diff-empty&quot;&gt;(No difference)&lt;/div&gt;
&lt;/td&gt;&lt;/tr&gt;&lt;/table&gt;</summary>
		<author><name>Editor</name></author>
	</entry>
	<entry>
		<id>https://lipidbank.jp/mediawiki/index.php?title=LBGTGccc:16000SC01:18000SC01:16000SC01_2&amp;diff=68529&amp;oldid=prev</id>
		<title>Editor at 13:00, 26 July 2009</title>
		<link rel="alternate" type="text/html" href="https://lipidbank.jp/mediawiki/index.php?title=LBGTGccc:16000SC01:18000SC01:16000SC01_2&amp;diff=68529&amp;oldid=prev"/>
		<updated>2009-07-26T13:00:00Z</updated>

		<summary type="html">&lt;p&gt;&lt;/p&gt;
&lt;p&gt;&lt;b&gt;New page&lt;/b&gt;&lt;/p&gt;&lt;div&gt;{{Lipid/Header}}&lt;br /&gt;
&lt;br /&gt;
{{Metabolite&lt;br /&gt;
|LipidBank=NAG5156&lt;br /&gt;
|SysName=Glycerol 1,3-dihexadecanoate 2- (9-octadecenoate)  (Z) -form&lt;br /&gt;
|Common Name=&amp;amp;&amp;amp;alpha,alpha-Dipalmitoolein&amp;amp;&amp;amp;2-Oleodipalmitin&amp;amp;&amp;amp;9-Octadecenoic acid 2- [  (1-oxohexadecyl)  oxy ] -1- [   [  (1-oxohexadecyl) oxy ]  methyl ]  ethyl ester&amp;amp;&amp;amp;Glycerol 1,3-dihexadecanoate 2- (9-octadecenoate)  (Z) -form&amp;amp;&amp;amp;&lt;br /&gt;
|Melting Point=Cryst.(acetone). Mp 37.2°C. Exhibits polymorphism. &amp;lt;FONT FACE=&amp;quot;Symbol&amp;quot;&amp;gt;b&amp;lt;/FONT&amp;gt;1=36.7°C. &amp;lt;&amp;lt;5144&amp;gt;&amp;gt;The crystal shows the typical polymorphism phenomenon. Knowledge and naming on got polymorphism are different by the researcher, and there is following correspondence on got polymolphism each. The crystallization phenomenon of the POP is greatly dependent on the polymorphism. By being dependent on the temperature of the crystallization, got polymorphism and the crystallization kinetic change.&lt;br /&gt;
|Solubility= 1.65 at 13.9°C, 1.30 at 13.6°C, 1.05 at 12.9°C, 0.80 at 11.5°C g solute/100g solvent in tetradecane&amp;lt;&amp;lt;5182&amp;gt;&amp;gt;&lt;br /&gt;
|NMR Spectra=13C-NMR spectra &amp;lt;&amp;lt;5183&amp;gt;&amp;gt;, &lt;br /&gt;
|NOTE Spectra=X-ray short spacing and long spacing &amp;lt;&amp;lt;5184&amp;gt;&amp;gt;, &lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
{{Lipid/Footer}}&lt;/div&gt;</summary>
		<author><name>Editor</name></author>
	</entry>
</feed>