LBF18108HP01: Difference between revisions

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|LipidMaps=LMFA01040010
|LipidMaps=LMFA01040010
|SysName=12,13-Epoxy-9-Hydroperoxy-10-Octadecenoic Acid
|SysName=12,13-Epoxy-9-Hydroperoxy-10-Octadecenoic Acid
|Common Name=&&12,13-Epoxy-9-Hydroperoxy-10-Octadecenoic Acid&&
|Mass Spectra=GC-EI-MS(after methanolysis, reduction and trimethylsilylation)[[Reference:Gardner_HW:Weisleder_D:Kleiman_R:,Lipids,1978,13,246|{{RelationTable/GetFirstAuthor|Reference:Gardner_HW:Weisleder_D:Kleiman_R:,Lipids,1978,13,246}}]][[Reference:Tokita_M:Morita_M:,Agric. Biol. Chem.,1987,51,309|{{RelationTable/GetFirstAuthor|Reference:Tokita_M:Morita_M:,Agric. Biol. Chem.,1987,51,309}}]]
|Mass Spectra=GC-EI-MS(after methanolysis, reduction and trimethylsilylation)[[Reference:Gardner_HW:Weisleder_D:Kleiman_R:,Lipids,1978,13,246|{{RelationTable/GetFirstAuthor|Reference:Gardner_HW:Weisleder_D:Kleiman_R:,Lipids,1978,13,246}}]][[Reference:Tokita_M:Morita_M:,Agric. Biol. Chem.,1987,51,309|{{RelationTable/GetFirstAuthor|Reference:Tokita_M:Morita_M:,Agric. Biol. Chem.,1987,51,309}}]]
|IR Spectra=Isorated trans unsaturation(970cm<SUP><FONT SIZE=-1>-</FONT></SUP><SUP><FONT SIZE=-1>1</FONT></SUP>), trans epoxide(885cm<SUP><FONT SIZE=-1>-</FONT></SUP><SUP><FONT SIZE=-1>1</FONT></SUP>), OOH(3600 AND 3430cm<SUP><FONT SIZE=-1>-</FONT></SUP><SUP><FONT SIZE=-1>1</FONT></SUP>) [[Reference:Gardner_HW:Weisleder_D:Kleiman_R:,Lipids,1978,13,246|{{RelationTable/GetFirstAuthor|Reference:Gardner_HW:Weisleder_D:Kleiman_R:,Lipids,1978,13,246}}]]
|IR Spectra=Isorated trans unsaturation(970cm<SUP><FONT SIZE=-1>-</FONT></SUP><SUP><FONT SIZE=-1>1</FONT></SUP>), trans epoxide(885cm<SUP><FONT SIZE=-1>-</FONT></SUP><SUP><FONT SIZE=-1>1</FONT></SUP>), OOH(3600 AND 3430cm<SUP><FONT SIZE=-1>-</FONT></SUP><SUP><FONT SIZE=-1>1</FONT></SUP>) [[Reference:Gardner_HW:Weisleder_D:Kleiman_R:,Lipids,1978,13,246|{{RelationTable/GetFirstAuthor|Reference:Gardner_HW:Weisleder_D:Kleiman_R:,Lipids,1978,13,246}}]]
|NMR Spectra=<SUP><FONT SIZE=-1>1</FONT></SUP>H-NMR(methyl ester)[[Reference:Gardner_HW:Weisleder_D:Kleiman_R:,Lipids,1978,13,246|{{RelationTable/GetFirstAuthor|Reference:Gardner_HW:Weisleder_D:Kleiman_R:,Lipids,1978,13,246}}]]: C9(4.33ppm), C10(5.85ppm), C11(5.47ppm), C12(3.11ppm), C13(2.84ppm) J10-11=16Hz(trans olefin), J12-13=2Hz(trans epoxide)
|NMR Spectra=<SUP><FONT SIZE=-1>1</FONT></SUP>H-NMR(methyl ester)[[Reference:Gardner_HW:Weisleder_D:Kleiman_R:,Lipids,1978,13,246|{{RelationTable/GetFirstAuthor|Reference:Gardner_HW:Weisleder_D:Kleiman_R:,Lipids,1978,13,246}}]]: C9(4.33ppm), C10(5.85ppm), C11(5.47ppm), C12(3.11ppm), C13(2.84ppm) J10-11=16Hz(trans olefin), J12-13=2Hz(trans epoxide)
}}
}}

Revision as of 08:19, 19 December 2008


Upper classes: LB LBF



12,13-Epoxy-9-Hydroperoxy-10-Octadecenoic Acid
LBF18108HP01.png
Structural Information
12,13-Epoxy-9-Hydroperoxy-10-Octadecenoic Acid
  • 12,13-Epoxy-9-Hydroperoxy-10-Octadecenoic Acid
Formula C18H32O5
Exact Mass 328.224974134
Average Mass 328.44368000000003
SMILES C(C(C=CC(OO)CCCCCCCC(O)=O)1)(CCCCC)O1
Physicochemical Information
Spectral Information
Mass Spectra GC-EI-MS(after methanolysis, reduction and trimethylsilylation) Gardner_HW et al. TokitaMet al.
UV Spectra
IR Spectra Isorated trans unsaturation(970cm-1), trans epoxide(885cm-1), OOH(3600 AND 3430cm-1) Gardner_HW et al.
NMR Spectra 1H-NMR(methyl ester) Gardner_HW et al.: C9(4.33ppm), C10(5.85ppm), C11(5.47ppm), C12(3.11ppm), C13(2.84ppm) J10-11=16Hz(trans olefin), J12-13=2Hz(trans epoxide)
Other Spectra
Chromatograms
Reported Metabolites, References
Biospecies ID Compound Name Reference Comment
n.a. LBF18108HP01 See above. Frankel_EN 1984
n.a. LBF18108HP01 See above. Fujimoto_K 1986
n.a. LBF18108HP01 See above. Gardner_HW 1975
n.a. LBF18108HP01 See above. Gardner_HW et al. 1978
n.a. LBF18108HP01 See above. Tokita_M et al. 1987
n.a. LBF18108HP01 See above. Wu_GS et al. 1977