https://lipidbank.jp/mediawiki/index.php?action=history&feed=atom&title=LBF08102BC02 2026-04-29T09:56:31Z Revision history for this page on the wiki MediaWiki 1.43.0 https://lipidbank.jp/mediawiki/index.php?title=LBF08102BC02&diff=42933&oldid=prev 2010-05-12T06:22:12Z

<p></p> <table style="background-color: #fff; color: #202122;" data-mw="interface"> <col class="diff-marker" /> <col class="diff-content" /> <col class="diff-marker" /> <col class="diff-content" /> <tr class="diff-title" lang="en"> <td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">← Older revision</td> <td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">Revision as of 15:22, 12 May 2010</td> </tr><tr><td colspan="2" class="diff-lineno" id="mw-diff-left-l9">Line 9:</td> <td colspan="2" class="diff-lineno">Line 9:</td></tr> <tr><td class="diff-marker"></td><td style="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;"><div>|Common Name=&amp;&amp;2,7-Dimethyl-6-octenoic acid&amp;&amp;</div></td><td class="diff-marker"></td><td style="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;"><div>|Common Name=&amp;&amp;2,7-Dimethyl-6-octenoic acid&amp;&amp;</div></td></tr> <tr><td class="diff-marker"></td><td style="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;"><div>|Boiling Point=146 - 147°C/13mmHg [[Reference:Ishimaru_H:,J. Chem. Soc. Japan. Pure Chem. Sec.,1955,76,1253|{{RelationTable/GetFirstAuthor|Reference:Ishimaru_H:,J. Chem. Soc. Japan. Pure Chem. Sec.,1955,76,1253}}]]</div></td><td class="diff-marker"></td><td style="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;"><div>|Boiling Point=146 - 147°C/13mmHg [[Reference:Ishimaru_H:,J. Chem. Soc. Japan. Pure Chem. Sec.,1955,76,1253|{{RelationTable/GetFirstAuthor|Reference:Ishimaru_H:,J. Chem. Soc. Japan. Pure Chem. Sec.,1955,76,1253}}]]</div></td></tr> <tr><td class="diff-marker" data-marker="−"></td><td style="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;"><div>|Density=D16/4 <del style="font-weight: bold; text-decoration: none;">= </del>0.9257 [[Reference:Ishimaru_H:,J. Chem. Soc. Japan. Pure Chem. Sec.,1955,76,1253|{{RelationTable/GetFirstAuthor|Reference:Ishimaru_H:,J. Chem. Soc. Japan. Pure Chem. Sec.,1955,76,1253}}]]</div></td><td class="diff-marker" data-marker="+"></td><td style="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;"><div>|Density=D16/4<ins style="font-weight: bold; text-decoration: none;">: </ins>0.9257 [[Reference:Ishimaru_H:,J. Chem. Soc. Japan. Pure Chem. Sec.,1955,76,1253|{{RelationTable/GetFirstAuthor|Reference:Ishimaru_H:,J. Chem. Soc. Japan. Pure Chem. Sec.,1955,76,1253}}]]</div></td></tr> <tr><td class="diff-marker"></td><td style="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;"><div>|Refractive= eta 16/D = 1.4502 [[Reference:Ishimaru_H:,J. Chem. Soc. Japan. Pure Chem. Sec.,1955,76,1253|{{RelationTable/GetFirstAuthor|Reference:Ishimaru_H:,J. Chem. Soc. Japan. Pure Chem. Sec.,1955,76,1253}}]]</div></td><td class="diff-marker"></td><td style="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;"><div>|Refractive= eta 16/D = 1.4502 [[Reference:Ishimaru_H:,J. Chem. Soc. Japan. Pure Chem. Sec.,1955,76,1253|{{RelationTable/GetFirstAuthor|Reference:Ishimaru_H:,J. Chem. Soc. Japan. Pure Chem. Sec.,1955,76,1253}}]]</div></td></tr> <tr><td class="diff-marker"></td><td style="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;"><div>|Source=</div></td><td class="diff-marker"></td><td style="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;"><div>|Source=</div></td></tr> <!-- diff cache key wikidb:diff:1.41:old-42932:rev-42933:php=table --> </table>

Editor https://lipidbank.jp/mediawiki/index.php?title=LBF08102BC02&diff=42932&oldid=prev 2010-04-14T21:00:00Z

<p></p> <table style="background-color: #fff; color: #202122;" data-mw="interface"> <col class="diff-marker" /> <col class="diff-content" /> <col class="diff-marker" /> <col class="diff-content" /> <tr class="diff-title" lang="en"> <td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">← Older revision</td> <td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">Revision as of 06:00, 15 April 2010</td> </tr><tr><td colspan="4" class="diff-notice" lang="en"><div class="mw-diff-empty">(No difference)</div> </td></tr> <!-- diff cache key wikidb:diff:1.41:old-42931:rev-42932 --> </table>

Editor https://lipidbank.jp/mediawiki/index.php?title=LBF08102BC02&diff=42931&oldid=prev 2010-04-09T06:18:34Z

<p></p> <table style="background-color: #fff; color: #202122;" data-mw="interface"> <col class="diff-marker" /> <col class="diff-content" /> <col class="diff-marker" /> <col class="diff-content" /> <tr class="diff-title" lang="en"> <td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">← Older revision</td> <td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">Revision as of 15:18, 9 April 2010</td> </tr><tr><td colspan="2" class="diff-lineno" id="mw-diff-left-l6">Line 6:</td> <td colspan="2" class="diff-lineno">Line 6:</td></tr> <tr><td class="diff-marker"></td><td style="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;"><div>|LipidBank=DFA7097</div></td><td class="diff-marker"></td><td style="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;"><div>|LipidBank=DFA7097</div></td></tr> <tr><td class="diff-marker"></td><td style="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;"><div>|LipidMaps=LMFA01020129</div></td><td class="diff-marker"></td><td style="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;"><div>|LipidMaps=LMFA01020129</div></td></tr> <tr><td class="diff-marker" data-marker="−"></td><td style="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;"><div>|SysName=2,7-Dimethyl-6-<del style="font-weight: bold; text-decoration: none;">Octenoic Acid</del></div></td><td class="diff-marker" data-marker="+"></td><td style="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;"><div>|SysName=2,7-Dimethyl-6-<ins style="font-weight: bold; text-decoration: none;">octenoic acid</ins></div></td></tr> <tr><td class="diff-marker" data-marker="−"></td><td style="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;"><div>|Common Name=&amp;&amp;2,7-Dimethyl-6-<del style="font-weight: bold; text-decoration: none;">Octenoic Acid</del>&amp;&amp;</div></td><td class="diff-marker" data-marker="+"></td><td style="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;"><div>|Common Name=&amp;&amp;2,7-Dimethyl-6-<ins style="font-weight: bold; text-decoration: none;">octenoic acid</ins>&amp;&amp;</div></td></tr> <tr><td class="diff-marker"></td><td style="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;"><div>|Boiling Point=146 - 147°C/13mmHg [[Reference:Ishimaru_H:,J. Chem. Soc. Japan. Pure Chem. Sec.,1955,76,1253|{{RelationTable/GetFirstAuthor|Reference:Ishimaru_H:,J. Chem. Soc. Japan. Pure Chem. Sec.,1955,76,1253}}]]</div></td><td class="diff-marker"></td><td style="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;"><div>|Boiling Point=146 - 147°C/13mmHg [[Reference:Ishimaru_H:,J. Chem. Soc. Japan. Pure Chem. Sec.,1955,76,1253|{{RelationTable/GetFirstAuthor|Reference:Ishimaru_H:,J. Chem. Soc. Japan. Pure Chem. Sec.,1955,76,1253}}]]</div></td></tr> <tr><td class="diff-marker"></td><td style="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;"><div>|Density=D16/4 = 0.9257 [[Reference:Ishimaru_H:,J. Chem. Soc. Japan. Pure Chem. Sec.,1955,76,1253|{{RelationTable/GetFirstAuthor|Reference:Ishimaru_H:,J. Chem. Soc. Japan. Pure Chem. Sec.,1955,76,1253}}]]</div></td><td class="diff-marker"></td><td style="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;"><div>|Density=D16/4 = 0.9257 [[Reference:Ishimaru_H:,J. Chem. Soc. Japan. Pure Chem. Sec.,1955,76,1253|{{RelationTable/GetFirstAuthor|Reference:Ishimaru_H:,J. Chem. Soc. Japan. Pure Chem. Sec.,1955,76,1253}}]]</div></td></tr> <!-- diff cache key wikidb:diff:1.41:old-42930:rev-42931:php=table --> </table>

Editor https://lipidbank.jp/mediawiki/index.php?title=LBF08102BC02&diff=42930&oldid=prev 2010-03-19T05:29:22Z

<p></p> <table style="background-color: #fff; color: #202122;" data-mw="interface"> <col class="diff-marker" /> <col class="diff-content" /> <col class="diff-marker" /> <col class="diff-content" /> <tr class="diff-title" lang="en"> <td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">← Older revision</td> <td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">Revision as of 14:29, 19 March 2010</td> </tr><tr><td colspan="2" class="diff-lineno" id="mw-diff-left-l12">Line 12:</td> <td colspan="2" class="diff-lineno">Line 12:</td></tr> <tr><td class="diff-marker"></td><td style="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;"><div>|Refractive= eta 16/D = 1.4502 [[Reference:Ishimaru_H:,J. Chem. Soc. Japan. Pure Chem. Sec.,1955,76,1253|{{RelationTable/GetFirstAuthor|Reference:Ishimaru_H:,J. Chem. Soc. Japan. Pure Chem. Sec.,1955,76,1253}}]]</div></td><td class="diff-marker"></td><td style="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;"><div>|Refractive= eta 16/D = 1.4502 [[Reference:Ishimaru_H:,J. Chem. Soc. Japan. Pure Chem. Sec.,1955,76,1253|{{RelationTable/GetFirstAuthor|Reference:Ishimaru_H:,J. Chem. Soc. Japan. Pure Chem. Sec.,1955,76,1253}}]]</div></td></tr> <tr><td class="diff-marker"></td><td style="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;"><div>|Source=</div></td><td class="diff-marker"></td><td style="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;"><div>|Source=</div></td></tr> <tr><td class="diff-marker" data-marker="−"></td><td style="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;"><div>|Chemical Synthesis=2,7-Dimethyl-6-octenoic acid was prepared from methyl-(5-methyl-4-hexenyl)-malonic acid diethyl and <del style="font-weight: bold; text-decoration: none;">koh </del>[[Reference:Ishimaru_H:,J. Chem. Soc. Japan. Pure Chem. Sec.,1955,76,1253|{{RelationTable/GetFirstAuthor|Reference:Ishimaru_H:,J. Chem. Soc. Japan. Pure Chem. Sec.,1955,76,1253}}]].</div></td><td class="diff-marker" data-marker="+"></td><td style="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;"><div>|Chemical Synthesis=2,7-Dimethyl-6-octenoic acid was prepared from methyl-(5-methyl-4-hexenyl)-malonic acid diethyl and <ins style="font-weight: bold; text-decoration: none;">KOH </ins>[[Reference:Ishimaru_H:,J. Chem. Soc. Japan. Pure Chem. Sec.,1955,76,1253|{{RelationTable/GetFirstAuthor|Reference:Ishimaru_H:,J. Chem. Soc. Japan. Pure Chem. Sec.,1955,76,1253}}]].</div></td></tr> <tr><td class="diff-marker"></td><td style="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;"><div>|Metabolism=</div></td><td class="diff-marker"></td><td style="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;"><div>|Metabolism=</div></td></tr> <tr><td class="diff-marker"></td><td style="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;"><div>}}</div></td><td class="diff-marker"></td><td style="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;"><div>}}</div></td></tr> <tr><td class="diff-marker"></td><td style="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;"><br></td><td class="diff-marker"></td><td style="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;"><br></td></tr> <tr><td class="diff-marker"></td><td style="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;"><div>{{Lipid/Footer}}</div></td><td class="diff-marker"></td><td style="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;"><div>{{Lipid/Footer}}</div></td></tr> <!-- diff cache key wikidb:diff:1.41:old-42929:rev-42930:php=table --> </table>

Dbmanager https://lipidbank.jp/mediawiki/index.php?title=LBF08102BC02&diff=42929&oldid=prev 2010-02-25T10:00:10Z

<p></p> <table style="background-color: #fff; color: #202122;" data-mw="interface"> <col class="diff-marker" /> <col class="diff-content" /> <col class="diff-marker" /> <col class="diff-content" /> <tr class="diff-title" lang="en"> <td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">← Older revision</td> <td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">Revision as of 19:00, 25 February 2010</td> </tr><tr><td colspan="4" class="diff-notice" lang="en"><div class="mw-diff-empty">(No difference)</div> </td></tr> <!-- diff cache key wikidb:diff:1.41:old-42928:rev-42929 --> </table>

Editor https://lipidbank.jp/mediawiki/index.php?title=LBF08102BC02&diff=42928&oldid=prev 2010-02-19T14:00:10Z

<p></p> <table style="background-color: #fff; color: #202122;" data-mw="interface"> <col class="diff-marker" /> <col class="diff-content" /> <col class="diff-marker" /> <col class="diff-content" /> <tr class="diff-title" lang="en"> <td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">← Older revision</td> <td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">Revision as of 23:00, 19 February 2010</td> </tr><tr><td colspan="2" class="diff-lineno" id="mw-diff-left-l10">Line 10:</td> <td colspan="2" class="diff-lineno">Line 10:</td></tr> <tr><td class="diff-marker"></td><td style="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;"><div>|Boiling Point=146 - 147°C/13mmHg [[Reference:Ishimaru_H:,J. Chem. Soc. Japan. Pure Chem. Sec.,1955,76,1253|{{RelationTable/GetFirstAuthor|Reference:Ishimaru_H:,J. Chem. Soc. Japan. Pure Chem. Sec.,1955,76,1253}}]]</div></td><td class="diff-marker"></td><td style="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;"><div>|Boiling Point=146 - 147°C/13mmHg [[Reference:Ishimaru_H:,J. Chem. Soc. Japan. Pure Chem. Sec.,1955,76,1253|{{RelationTable/GetFirstAuthor|Reference:Ishimaru_H:,J. Chem. Soc. Japan. Pure Chem. Sec.,1955,76,1253}}]]</div></td></tr> <tr><td class="diff-marker"></td><td style="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;"><div>|Density=D16/4 = 0.9257 [[Reference:Ishimaru_H:,J. Chem. Soc. Japan. Pure Chem. Sec.,1955,76,1253|{{RelationTable/GetFirstAuthor|Reference:Ishimaru_H:,J. Chem. Soc. Japan. Pure Chem. Sec.,1955,76,1253}}]]</div></td><td class="diff-marker"></td><td style="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;"><div>|Density=D16/4 = 0.9257 [[Reference:Ishimaru_H:,J. Chem. Soc. Japan. Pure Chem. Sec.,1955,76,1253|{{RelationTable/GetFirstAuthor|Reference:Ishimaru_H:,J. Chem. Soc. Japan. Pure Chem. Sec.,1955,76,1253}}]]</div></td></tr> <tr><td class="diff-marker" data-marker="−"></td><td style="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;"><div>|Refractive=<del style="font-weight: bold; text-decoration: none;">eta16</del>/D = 1.4502 [[Reference:Ishimaru_H:,J. Chem. Soc. Japan. Pure Chem. Sec.,1955,76,1253|{{RelationTable/GetFirstAuthor|Reference:Ishimaru_H:,J. Chem. Soc. Japan. Pure Chem. Sec.,1955,76,1253}}]]</div></td><td class="diff-marker" data-marker="+"></td><td style="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;"><div>|Refractive= <ins style="font-weight: bold; text-decoration: none;">eta 16</ins>/D = 1.4502 [[Reference:Ishimaru_H:,J. Chem. Soc. Japan. Pure Chem. Sec.,1955,76,1253|{{RelationTable/GetFirstAuthor|Reference:Ishimaru_H:,J. Chem. Soc. Japan. Pure Chem. Sec.,1955,76,1253}}]]</div></td></tr> <tr><td class="diff-marker"></td><td style="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;"><div>|Source=</div></td><td class="diff-marker"></td><td style="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;"><div>|Source=</div></td></tr> <tr><td class="diff-marker"></td><td style="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;"><div>|Chemical Synthesis=2,7-Dimethyl-6-octenoic acid was prepared from methyl-(5-methyl-4-hexenyl)-malonic acid diethyl and koh [[Reference:Ishimaru_H:,J. Chem. Soc. Japan. Pure Chem. Sec.,1955,76,1253|{{RelationTable/GetFirstAuthor|Reference:Ishimaru_H:,J. Chem. Soc. Japan. Pure Chem. Sec.,1955,76,1253}}]].</div></td><td class="diff-marker"></td><td style="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;"><div>|Chemical Synthesis=2,7-Dimethyl-6-octenoic acid was prepared from methyl-(5-methyl-4-hexenyl)-malonic acid diethyl and koh [[Reference:Ishimaru_H:,J. Chem. Soc. Japan. Pure Chem. Sec.,1955,76,1253|{{RelationTable/GetFirstAuthor|Reference:Ishimaru_H:,J. Chem. Soc. Japan. Pure Chem. Sec.,1955,76,1253}}]].</div></td></tr> <!-- diff cache key wikidb:diff:1.41:old-42927:rev-42928:php=table --> </table>

Editor https://lipidbank.jp/mediawiki/index.php?title=LBF08102BC02&diff=42927&oldid=prev 2010-02-19T14:00:00Z

<p></p> <table style="background-color: #fff; color: #202122;" data-mw="interface"> <col class="diff-marker" /> <col class="diff-content" /> <col class="diff-marker" /> <col class="diff-content" /> <tr class="diff-title" lang="en"> <td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">← Older revision</td> <td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">Revision as of 23:00, 19 February 2010</td> </tr><tr><td colspan="2" class="diff-lineno" id="mw-diff-left-l10">Line 10:</td> <td colspan="2" class="diff-lineno">Line 10:</td></tr> <tr><td class="diff-marker"></td><td style="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;"><div>|Boiling Point=146 - 147°C/13mmHg [[Reference:Ishimaru_H:,J. Chem. Soc. Japan. Pure Chem. Sec.,1955,76,1253|{{RelationTable/GetFirstAuthor|Reference:Ishimaru_H:,J. Chem. Soc. Japan. Pure Chem. Sec.,1955,76,1253}}]]</div></td><td class="diff-marker"></td><td style="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;"><div>|Boiling Point=146 - 147°C/13mmHg [[Reference:Ishimaru_H:,J. Chem. Soc. Japan. Pure Chem. Sec.,1955,76,1253|{{RelationTable/GetFirstAuthor|Reference:Ishimaru_H:,J. Chem. Soc. Japan. Pure Chem. Sec.,1955,76,1253}}]]</div></td></tr> <tr><td class="diff-marker"></td><td style="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;"><div>|Density=D16/4 = 0.9257 [[Reference:Ishimaru_H:,J. Chem. Soc. Japan. Pure Chem. Sec.,1955,76,1253|{{RelationTable/GetFirstAuthor|Reference:Ishimaru_H:,J. Chem. Soc. Japan. Pure Chem. Sec.,1955,76,1253}}]]</div></td><td class="diff-marker"></td><td style="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;"><div>|Density=D16/4 = 0.9257 [[Reference:Ishimaru_H:,J. Chem. Soc. Japan. Pure Chem. Sec.,1955,76,1253|{{RelationTable/GetFirstAuthor|Reference:Ishimaru_H:,J. Chem. Soc. Japan. Pure Chem. Sec.,1955,76,1253}}]]</div></td></tr> <tr><td class="diff-marker" data-marker="−"></td><td style="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;"><div>|Refractive=<del style="font-weight: bold; text-decoration: none;">&lt;FONT FACE="Symbol"&gt;h&lt;/FONT&gt;16</del>/D = 1.4502 [[Reference:Ishimaru_H:,J. Chem. Soc. Japan. Pure Chem. Sec.,1955,76,1253|{{RelationTable/GetFirstAuthor|Reference:Ishimaru_H:,J. Chem. Soc. Japan. Pure Chem. Sec.,1955,76,1253}}]]</div></td><td class="diff-marker" data-marker="+"></td><td style="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;"><div>|Refractive=<ins style="font-weight: bold; text-decoration: none;">eta16</ins>/D = 1.4502 [[Reference:Ishimaru_H:,J. Chem. Soc. Japan. Pure Chem. Sec.,1955,76,1253|{{RelationTable/GetFirstAuthor|Reference:Ishimaru_H:,J. Chem. Soc. Japan. Pure Chem. Sec.,1955,76,1253}}]]</div></td></tr> <tr><td class="diff-marker"></td><td style="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;"><div>|Source=</div></td><td class="diff-marker"></td><td style="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;"><div>|Source=</div></td></tr> <tr><td class="diff-marker"></td><td style="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;"><div>|Chemical Synthesis=2,7-Dimethyl-6-octenoic acid was prepared from methyl-(5-methyl-4-hexenyl)-malonic acid diethyl and koh [[Reference:Ishimaru_H:,J. Chem. Soc. Japan. Pure Chem. Sec.,1955,76,1253|{{RelationTable/GetFirstAuthor|Reference:Ishimaru_H:,J. Chem. Soc. Japan. Pure Chem. Sec.,1955,76,1253}}]].</div></td><td class="diff-marker"></td><td style="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;"><div>|Chemical Synthesis=2,7-Dimethyl-6-octenoic acid was prepared from methyl-(5-methyl-4-hexenyl)-malonic acid diethyl and koh [[Reference:Ishimaru_H:,J. Chem. Soc. Japan. Pure Chem. Sec.,1955,76,1253|{{RelationTable/GetFirstAuthor|Reference:Ishimaru_H:,J. Chem. Soc. Japan. Pure Chem. Sec.,1955,76,1253}}]].</div></td></tr> <!-- diff cache key wikidb:diff:1.41:old-42926:rev-42927:php=table --> </table>

Editor https://lipidbank.jp/mediawiki/index.php?title=LBF08102BC02&diff=42926&oldid=prev 2010-01-06T21:00:00Z

<p></p> <table style="background-color: #fff; color: #202122;" data-mw="interface"> <col class="diff-marker" /> <col class="diff-content" /> <col class="diff-marker" /> <col class="diff-content" /> <tr class="diff-title" lang="en"> <td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">← Older revision</td> <td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">Revision as of 06:00, 7 January 2010</td> </tr><tr><td colspan="2" class="diff-lineno" id="mw-diff-left-l10">Line 10:</td> <td colspan="2" class="diff-lineno">Line 10:</td></tr> <tr><td class="diff-marker"></td><td style="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;"><div>|Boiling Point=146 - 147°C/13mmHg [[Reference:Ishimaru_H:,J. Chem. Soc. Japan. Pure Chem. Sec.,1955,76,1253|{{RelationTable/GetFirstAuthor|Reference:Ishimaru_H:,J. Chem. Soc. Japan. Pure Chem. Sec.,1955,76,1253}}]]</div></td><td class="diff-marker"></td><td style="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;"><div>|Boiling Point=146 - 147°C/13mmHg [[Reference:Ishimaru_H:,J. Chem. Soc. Japan. Pure Chem. Sec.,1955,76,1253|{{RelationTable/GetFirstAuthor|Reference:Ishimaru_H:,J. Chem. Soc. Japan. Pure Chem. Sec.,1955,76,1253}}]]</div></td></tr> <tr><td class="diff-marker"></td><td style="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;"><div>|Density=D16/4 = 0.9257 [[Reference:Ishimaru_H:,J. Chem. Soc. Japan. Pure Chem. Sec.,1955,76,1253|{{RelationTable/GetFirstAuthor|Reference:Ishimaru_H:,J. Chem. Soc. Japan. Pure Chem. Sec.,1955,76,1253}}]]</div></td><td class="diff-marker"></td><td style="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;"><div>|Density=D16/4 = 0.9257 [[Reference:Ishimaru_H:,J. Chem. Soc. Japan. Pure Chem. Sec.,1955,76,1253|{{RelationTable/GetFirstAuthor|Reference:Ishimaru_H:,J. Chem. Soc. Japan. Pure Chem. Sec.,1955,76,1253}}]]</div></td></tr> <tr><td class="diff-marker" data-marker="−"></td><td style="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;"><div>|<del style="font-weight: bold; text-decoration: none;">Optical</del>=&lt;FONT FACE="Symbol"&gt;h&lt;/FONT&gt;16/D = 1.4502 [[Reference:Ishimaru_H:,J. Chem. Soc. Japan. Pure Chem. Sec.,1955,76,1253|{{RelationTable/GetFirstAuthor|Reference:Ishimaru_H:,J. Chem. Soc. Japan. Pure Chem. Sec.,1955,76,1253}}]]</div></td><td class="diff-marker" data-marker="+"></td><td style="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;"><div>|<ins style="font-weight: bold; text-decoration: none;">Refractive</ins>=&lt;FONT FACE="Symbol"&gt;h&lt;/FONT&gt;16/D = 1.4502 [[Reference:Ishimaru_H:,J. Chem. Soc. Japan. Pure Chem. Sec.,1955,76,1253|{{RelationTable/GetFirstAuthor|Reference:Ishimaru_H:,J. Chem. Soc. Japan. Pure Chem. Sec.,1955,76,1253}}]]</div></td></tr> <tr><td class="diff-marker"></td><td style="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;"><div>|Source=</div></td><td class="diff-marker"></td><td style="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;"><div>|Source=</div></td></tr> <tr><td class="diff-marker"></td><td style="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;"><div>|Chemical Synthesis=2,7-Dimethyl-6-octenoic acid was prepared from methyl-(5-methyl-4-hexenyl)-malonic acid diethyl and koh [[Reference:Ishimaru_H:,J. Chem. Soc. Japan. Pure Chem. Sec.,1955,76,1253|{{RelationTable/GetFirstAuthor|Reference:Ishimaru_H:,J. Chem. Soc. Japan. Pure Chem. Sec.,1955,76,1253}}]].</div></td><td class="diff-marker"></td><td style="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;"><div>|Chemical Synthesis=2,7-Dimethyl-6-octenoic acid was prepared from methyl-(5-methyl-4-hexenyl)-malonic acid diethyl and koh [[Reference:Ishimaru_H:,J. Chem. Soc. Japan. Pure Chem. Sec.,1955,76,1253|{{RelationTable/GetFirstAuthor|Reference:Ishimaru_H:,J. Chem. Soc. Japan. Pure Chem. Sec.,1955,76,1253}}]].</div></td></tr> <!-- diff cache key wikidb:diff:1.41:old-42925:rev-42926:php=table --> </table>

Editor https://lipidbank.jp/mediawiki/index.php?title=LBF08102BC02&diff=42925&oldid=prev 2009-11-25T11:55:00Z

<p></p> <table style="background-color: #fff; color: #202122;" data-mw="interface"> <col class="diff-marker" /> <col class="diff-content" /> <col class="diff-marker" /> <col class="diff-content" /> <tr class="diff-title" lang="en"> <td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">← Older revision</td> <td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">Revision as of 20:55, 25 November 2009</td> </tr><tr><td colspan="2" class="diff-lineno" id="mw-diff-left-l12">Line 12:</td> <td colspan="2" class="diff-lineno">Line 12:</td></tr> <tr><td class="diff-marker"></td><td style="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;"><div>|Optical=&lt;FONT FACE=&quot;Symbol&quot;&gt;h&lt;/FONT&gt;16/D = 1.4502 [[Reference:Ishimaru_H:,J. Chem. Soc. Japan. Pure Chem. Sec.,1955,76,1253|{{RelationTable/GetFirstAuthor|Reference:Ishimaru_H:,J. Chem. Soc. Japan. Pure Chem. Sec.,1955,76,1253}}]]</div></td><td class="diff-marker"></td><td style="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;"><div>|Optical=&lt;FONT FACE=&quot;Symbol&quot;&gt;h&lt;/FONT&gt;16/D = 1.4502 [[Reference:Ishimaru_H:,J. Chem. Soc. Japan. Pure Chem. Sec.,1955,76,1253|{{RelationTable/GetFirstAuthor|Reference:Ishimaru_H:,J. Chem. Soc. Japan. Pure Chem. Sec.,1955,76,1253}}]]</div></td></tr> <tr><td class="diff-marker"></td><td style="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;"><div>|Source=</div></td><td class="diff-marker"></td><td style="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;"><div>|Source=</div></td></tr> <tr><td class="diff-marker" data-marker="−"></td><td style="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;"><div>|Chemical Synthesis=2,7-Dimethyl-6-octenoic acid was prepared from methyl-(5-methyl-4-hexenyl)-malonic acid diethyl and koh [[Reference:Ishimaru_H:,J. Chem. Soc. Japan. Pure Chem. Sec.,1955,76,1253|{{RelationTable/GetFirstAuthor|Reference:Ishimaru_H:,J. Chem. Soc. Japan. Pure Chem. Sec.,1955,76,1253}}]]<del style="font-weight: bold; text-decoration: none;">;&gt;</del>.</div></td><td class="diff-marker" data-marker="+"></td><td style="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;"><div>|Chemical Synthesis=2,7-Dimethyl-6-octenoic acid was prepared from methyl-(5-methyl-4-hexenyl)-malonic acid diethyl and koh [[Reference:Ishimaru_H:,J. Chem. Soc. Japan. Pure Chem. Sec.,1955,76,1253|{{RelationTable/GetFirstAuthor|Reference:Ishimaru_H:,J. Chem. Soc. Japan. Pure Chem. Sec.,1955,76,1253}}]].</div></td></tr> <tr><td class="diff-marker"></td><td style="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;"><div>|Metabolism=</div></td><td class="diff-marker"></td><td style="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;"><div>|Metabolism=</div></td></tr> <tr><td class="diff-marker"></td><td style="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;"><div>}}</div></td><td class="diff-marker"></td><td style="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;"><div>}}</div></td></tr> <tr><td class="diff-marker"></td><td style="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;"><br></td><td class="diff-marker"></td><td style="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;"><br></td></tr> <tr><td class="diff-marker"></td><td style="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;"><div>{{Lipid/Footer}}</div></td><td class="diff-marker"></td><td style="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;"><div>{{Lipid/Footer}}</div></td></tr> <!-- diff cache key wikidb:diff:1.41:old-42924:rev-42925:php=table --> </table>

Editor https://lipidbank.jp/mediawiki/index.php?title=LBF08102BC02&diff=42924&oldid=prev 2009-11-25T10:00:00Z

<p></p> <table style="background-color: #fff; color: #202122;" data-mw="interface"> <col class="diff-marker" /> <col class="diff-content" /> <col class="diff-marker" /> <col class="diff-content" /> <tr class="diff-title" lang="en"> <td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">← Older revision</td> <td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">Revision as of 19:00, 25 November 2009</td> </tr><tr><td colspan="4" class="diff-notice" lang="en"><div class="mw-diff-empty">(No difference)</div> </td></tr> <!-- diff cache key wikidb:diff:1.41:old-42923:rev-42924 --> </table>

Editor