LBF18106HO02: Difference between revisions

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|LipidMaps=LMFA01050126
|LipidMaps=LMFA01050126
|SysName=9,10-Dihydroxy-12-Octadecenoic Acid
|SysName=9,10-Dihydroxy-12-Octadecenoic Acid
|Mass Spectra=GC-EI-MS(after methanolysis and trimethylsilylation)<<8059/8071>>: m/e=457[M-CH3], 441[M-OCH3], 382[M-HOTMS], 361[SMTO=CH-CH(OTMS)-(CH2)7COOCH3], 271[361-HOTMS], 259[SMTO=CH-(CH2)7COOCH3], GC-EI-MS(after methanolysis, hydrogenation and trimethylsilylation)<<8059>>
|Mass Spectra=GC-EI-MS(after methanolysis and trimethylsilylation)[[Reference:Streckert_G:Stan_HJ:,Lipids,1975,10,847|{{RelationTable/GetFirstAuthor|Reference:Streckert_G:Stan_HJ:,Lipids,1975,10,847}}]][[Reference:Sessa_DJ:Gardner_HW:Kleiman_R:Weisleder_D:,Lipids,1977,12,613|{{RelationTable/GetFirstAuthor|Reference:Sessa_DJ:Gardner_HW:Kleiman_R:Weisleder_D:,Lipids,1977,12,613}}]]: m/e=457[M-CH3], 441[M-OCH3], 382[M-HOTMS], 361[SMTO=CH-CH(OTMS)-(CH2)7COOCH3], 271[361-HOTMS], 259[SMTO=CH-(CH2)7COOCH3], GC-EI-MS(after methanolysis, hydrogenation and trimethylsilylation)[[Reference:Streckert_G:Stan_HJ:,Lipids,1975,10,847|{{RelationTable/GetFirstAuthor|Reference:Streckert_G:Stan_HJ:,Lipids,1975,10,847}}]]
|IR Spectra=Methyl ester<<8071>>
|IR Spectra=Methyl ester[[Reference:Sessa_DJ:Gardner_HW:Kleiman_R:Weisleder_D:,Lipids,1977,12,613|{{RelationTable/GetFirstAuthor|Reference:Sessa_DJ:Gardner_HW:Kleiman_R:Weisleder_D:,Lipids,1977,12,613}}]]
}}
}}

Revision as of 00:00, 12 December 2008


Upper classes: LB LBF



GlcNAca/b1-3Xyla-4Galb1-3GalNAca1-4(NeuAc?1-2NeuGc4Mea1-3)GalNAcb1-4(EtnP-6)GlcNAcb1-3Manb1-4Glcb1-1Cer
LBF18106HO02.png
Structural Information
9,10-Dihydroxy-12-Octadecenoic Acid
Formula C18H34O4
Exact Mass 314.24570957599997
Average Mass 314.46016
SMILES CCCCCC=CCC(O)C(O)CCCCCCCC(O)=O
Physicochemical Information
Spectral Information
Mass Spectra GC-EI-MS(after methanolysis and trimethylsilylation) StreckertGet al. Sessa_DJ et al.: m/e=457[M-CH3], 441[M-OCH3], 382[M-HOTMS], 361[SMTO=CH-CH(OTMS)-(CH2)7COOCH3], 271[361-HOTMS], 259[SMTO=CH-(CH2)7COOCH3], GC-EI-MS(after methanolysis, hydrogenation and trimethylsilylation) StreckertGet al.
UV Spectra
IR Spectra Methyl ester Sessa_DJ et al.
NMR Spectra
Other Spectra
Chromatograms
Reported Metabolites, References
Biospecies ID Compound Name Reference Comment
n.a. LBF18106HO02 See above. Sessa_DJ et al. 1977
n.a. LBF18106HO02 See above. Streckert_G et al. 1975