LBF18206HO03: Difference between revisions

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|LipidMaps=LMFA01050124
|LipidMaps=LMFA01050124
|SysName=9-Hydroxy-10,12-Octadecadienoic Acid/9-Hydroxy-10,12-Octadecadienoate
|SysName=9-Hydroxy-10,12-Octadecadienoic Acid/9-Hydroxy-10,12-Octadecadienoate
|Common Name=&&9-Hydroxy-10,12-Octadecadienoic Acid/9-Hydroxy-10,12-Octadecadienoate&&
|Common Name=&&9-Hydroxy-10,12-Octadecadienoic Acid&&9-Hydroxy-10,12-Octadecadienoate&&
|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:Kleiman_R:Spencer_GF:,J. Am. Oil Chem. Soc.,1973,50,31|{{RelationTable/GetFirstAuthor|Reference:Kleiman_R:Spencer_GF:,J. Am. Oil Chem. Soc.,1973,50,31}}]][[Reference:Frankel_EN:Neff_WE:Rohwedder_WK:Khambay_BP:Garwood_RF:Weedon_BC:,Lipids,1977,12,908|{{RelationTable/GetFirstAuthor|Reference:Frankel_EN:Neff_WE:Rohwedder_WK:Khambay_BP:Garwood_RF:Weedon_BC:,Lipids,1977,12,908}}]]: m/e=382[M], 367[M-CH3], 351[M-OCH3], 311[M-(CH2)4CH3], 225[M-(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}}]], GC-EI-MS(after methanolysis and hydrogenation)[[Reference:Christophersen_BO:,Biochim. Biophys. Acta,1968,164,35|{{RelationTable/GetFirstAuthor|Reference:Christophersen_BO:,Biochim. Biophys. Acta,1968,164,35}}]]
|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:Kleiman_R:Spencer_GF:,J. Am. Oil Chem. Soc.,1973,50,31|{{RelationTable/GetFirstAuthor|Reference:Kleiman_R:Spencer_GF:,J. Am. Oil Chem. Soc.,1973,50,31}}]][[Reference:Frankel_EN:Neff_WE:Rohwedder_WK:Khambay_BP:Garwood_RF:Weedon_BC:,Lipids,1977,12,908|{{RelationTable/GetFirstAuthor|Reference:Frankel_EN:Neff_WE:Rohwedder_WK:Khambay_BP:Garwood_RF:Weedon_BC:,Lipids,1977,12,908}}]]: m/e=382[M], 367[M-CH3], 351[M-OCH3], 311[M-(CH2)4CH3], 225[M-(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}}]], GC-EI-MS(after methanolysis and hydrogenation)[[Reference:Christophersen_BO:,Biochim. Biophys. Acta,1968,164,35|{{RelationTable/GetFirstAuthor|Reference:Christophersen_BO:,Biochim. Biophys. Acta,1968,164,35}}]]
|UV Spectra=Methyl ester: <FONT FACE="Symbol">l</FONT>/max=231, 233, 234nm [[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}}]]
|UV Spectra=Methyl ester: <FONT FACE="Symbol">l</FONT>/max=231, 233, 234nm [[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 00:02, 20 December 2008


Upper classes: LB LBF



IDs and Links
LipidBank DFA8022
LipidMaps LMFA01050124
CAS
KEGG {{{KEGG}}}
KNApSAcK {{{KNApSAcK}}}
mol LBF18206HO03
9-Hydroxy-10,12-Octadecadienoic Acid
LBF18206HO03.png
Structural Information
9-Hydroxy-10,12-Octadecadienoic Acid/9-Hydroxy-10,12-Octadecadienoate
  • 9-Hydroxy-10,12-Octadecadienoic Acid
  • 9-Hydroxy-10,12-Octadecadienoate
Formula C18H32O3
Exact Mass 296.23514489
Average Mass 296.44488
SMILES CCCCCC=CC=CC(O)CCCCCCCC(O)=O
Physicochemical Information
Spectral Information
Mass Spectra GC-EI-MS(after methanolysis and trimethylsilylation) StreckertGet al. KleimanRet al. Frankel_EN et al.: m/e=382[M], 367[M-CH3], 351[M-OCH3], 311[M-(CH2)4CH3], 225[M-(CH2)7COOCH3], GC-EI-MS(after methanolysis, hydrogenation and trimethylsilylation) StreckertGet al., GC-EI-MS(after methanolysis and hydrogenation) Christophersen_BO
UV Spectra Methyl ester: l/max=231, 233, 234nm Sessa_DJ et al.
IR Spectra Methyl ester: trans, trans isomer: trans, trans conjugated diene(985cm-1), free OH(3600cm-1), bonded OH(3695-3318cm-1), trans, cis isomer: trans, cis conjugated diene(990, 968cm-1), olefinic(3005cm-1), free OH(3600cm-1), bonded OH(3700-3160cm-
NMR Spectra 1H-NMR(methyl ester): trans, trans olefinic protons(5.41ppm), trans,cis olefinic protons(5.91ppm), C9(4.15-4.20ppm), C14(2.07-2.10ppm) Neff_WE et al. Sessa_DJ et al.
Other Spectra
Chromatograms
Reported Metabolites, References
Biospecies ID Compound Name Reference Comment
n.a. LBF18206HO03 See above. Christophersen_BO 1968
n.a. LBF18206HO03 See above. Frankel_EN et al. 1977
n.a. LBF18206HO03 See above. Fujimoto_K 1986
n.a. LBF18206HO03 See above. Kleiman_R et al. 1973
n.a. LBF18206HO03 See above. Neff_WE et al. 1978
n.a. LBF18206HO03 See above. Sessa_DJ et al. 1977
n.a. LBF18206HO03 See above. Streckert_G et al. 1975
n.a. LBF18206HO03 See above. Yamamoto_Y et al. 1984
n.a. LBF18206HO03 See above. Yamamoto_Y et al. 1984
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