LBF18203EO02: Difference between revisions

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|Common Name=&&Methyl-12,13-Epoxy-9,15-Octadecadienoate&&
|Common Name=&&Methyl-12,13-Epoxy-9,15-Octadecadienoate&&
|Mass Spectra=GC-EI-MS[[Reference:Neff_WE:Frankel_EN:Weisleder_D:,Lipids,1982,17,780|{{RelationTable/GetFirstAuthor|Reference:Neff_WE:Frankel_EN:Weisleder_D:,Lipids,1982,17,780}}]]: m/e=308[M]; 277[M-OCH3]; 211[CH-(O)-CHCH2CH=CH(CH2)7COOCH3-28] 83[M-CH2CH=CH(CH2)7COOCH3-28], GC-EI-MS(after hydrogenation)(105): m/e=281[M-OCH3]; 241[CH-(O)-CH(CH2)10CO OCH3]; 213[214-28]; 113[M-(CH2)10COOCH3]; 85[113-28]
|Mass Spectra=GC-EI-MS[[Reference:Neff_WE:Frankel_EN:Weisleder_D:,Lipids,1982,17,780|{{RelationTable/GetFirstAuthor|Reference:Neff_WE:Frankel_EN:Weisleder_D:,Lipids,1982,17,780}}]]: m/e=308[M]; 277[M-OCH3]; 211[CH-(O)-CHCH2CH=CH(CH2)7COOCH3-28] 83[M-CH2CH=CH(CH2)7COOCH3-28], GC-EI-MS(after hydrogenation)(105): m/e=281[M-OCH3]; 241[CH-(O)-CH(CH2)10CO OCH3]; 213[214-28]; 113[M-(CH2)10COOCH3]; 85[113-28]
|IR Spectra=Cis unsaturation: 3002cm^- ^1 [[Reference:Neff_WE:Frankel_EN:Weisleder_D:,Lipids,1981,16,439|{{RelationTable/GetFirstAuthor|Reference:Neff_WE:Frankel_EN:Weisleder_D:,Lipids,1981,16,439}}]]
|IR Spectra=Cis unsaturation: 3002cm^{-1}[[Reference:Neff_WE:Frankel_EN:Weisleder_D:,Lipids,1981,16,439|{{RelationTable/GetFirstAuthor|Reference:Neff_WE:Frankel_EN:Weisleder_D:,Lipids,1981,16,439}}]]
|NMR Spectra=^1 H-NMR[[Reference:Neff_WE:Frankel_EN:Weisleder_D:,Lipids,1981,16,439|{{RelationTable/GetFirstAuthor|Reference:Neff_WE:Frankel_EN:Weisleder_D:,Lipids,1981,16,439}}]]: cis unsaturationS: 5.43ppm[4H]; cis epoxide ring:2.79 and 2.98ppm[2H]
|NMR Spectra=^1 H-NMR[[Reference:Neff_WE:Frankel_EN:Weisleder_D:,Lipids,1981,16,439|{{RelationTable/GetFirstAuthor|Reference:Neff_WE:Frankel_EN:Weisleder_D:,Lipids,1981,16,439}}]]: cis unsaturationS: 5.43ppm[4H]; cis epoxide ring:2.79 and 2.98ppm[2H]
|Source=Autooxidation of linoleate[[Reference:Neff_WE:Frankel_EN:Weisleder_D:,Lipids,1981,16,439|{{RelationTable/GetFirstAuthor|Reference:Neff_WE:Frankel_EN:Weisleder_D:,Lipids,1981,16,439}}]]. Photoenhancement of linoleate peroxidation[[Reference:Neff_WE:Frankel_EN:Weisleder_D:,Lipids,1982,17,780|{{RelationTable/GetFirstAuthor|Reference:Neff_WE:Frankel_EN:Weisleder_D:,Lipids,1982,17,780}}]].
|Source=Autooxidation of linoleate[[Reference:Neff_WE:Frankel_EN:Weisleder_D:,Lipids,1981,16,439|{{RelationTable/GetFirstAuthor|Reference:Neff_WE:Frankel_EN:Weisleder_D:,Lipids,1981,16,439}}]]. Photoenhancement of linoleate peroxidation[[Reference:Neff_WE:Frankel_EN:Weisleder_D:,Lipids,1982,17,780|{{RelationTable/GetFirstAuthor|Reference:Neff_WE:Frankel_EN:Weisleder_D:,Lipids,1982,17,780}}]].

Revision as of 10:00, 25 February 2010

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Upper classes: LB LBF



Methyl-12,13-Epoxy-9,15-Octadecadienoate
LBF18203EO02.png
Structural Information
Methyl-12,13-Epoxy-9,15-Octadecadienoate
  • Methyl-12,13-Epoxy-9,15-Octadecadienoate
Formula C19H32O3
Exact Mass 308.23514489
Average Mass 308.45558
SMILES C(C(CC=CCCCCCCCC(=O)OC)1)(CC=CCC)O1
Physicochemical Information
Autooxidation of linoleate Neff_WE et al.. Photoenhancement of linoleate peroxidation Neff_WE et al..
Spectral Information
Mass Spectra GC-EI-MS Neff_WE et al.: m/e=308[M]; 277[M-OCH3]; 211[CH-(O)-CHCH2CH=CH(CH2)7COOCH3-28] 83[M-CH2CH=CH(CH2)7COOCH3-28], GC-EI-MS(after hydrogenation)(105): m/e=281[M-OCH3]; 241[CH-(O)-CH(CH2)10CO OCH3]; 213[214-28]; 113[M-(CH2)10COOCH3]; 85[113-28]
UV Spectra
IR Spectra Cis unsaturation: 3002cm-1 Neff_WE et al.
NMR Spectra 1H-NMR Neff_WE et al.: cis unsaturationS: 5.43ppm[4H]; cis epoxide ring:2.79 and 2.98ppm[2H]
Other Spectra
Chromatograms
Reported Metabolites, References
Biospecies ID Compound Name Reference Comment
n.a. LBF18203EO02 See above. Neff_WE et al. 1981
n.a. LBF18203EO02 See above. Neff_WE et al. 1982