LBF18303SC02: Difference between revisions

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|LipidBank=DFA0192
|LipidBank=DFA0192
|LipidMaps=LMFA01030153
|LipidMaps=LMFA01030153
|SysName=trans-9, trans-12, trans-15-Octadecatrienoic acid
|SysName=(trans-9,trans-12,trans-15) -Octadecatrienoic acid
|Common Name=&&Elaidolinoleic acid&&trans-9, trans-12, trans-15-Octadecatrienoic acid&&
|Common Name=&&(9E,12E,15E) -Octadecatrienoic acid&&Elaidolinoleic acid&&
|Melting Point=29.5-30°C
|Melting Point=29.5-30°C
|Solubility=solubule in methylalcohol and petroleum ether.[[Reference:Kass_JP:Nichols_J:Burr_GO:,J. Am. Chem. Soc.,1941,63,1060|{{RelationTable/GetFirstAuthor|Reference:Kass_JP:Nichols_J:Burr_GO:,J. Am. Chem. Soc.,1941,63,1060}}]]
|Solubility=solubule in methyl alcohol and petroleum ether.[[Reference:Kass_JP:Nichols_J:Burr_GO:,J. Am. Chem. Soc.,1941,63,1060|{{RelationTable/GetFirstAuthor|Reference:Kass_JP:Nichols_J:Burr_GO:,J. Am. Chem. Soc.,1941,63,1060}}]]
|Source=
|Source=
|Chemical Synthesis=Synthetic, by treatment of the ester form of  alpha -linolenic acid with 1% Se at 205-215°C to yield this acid ester (melting point, 29-30°C).
|Chemical Synthesis=Synthetic, by treatment of the ester form of  alpha -linolenic acid with 1% Se at 205-215°C to yield this acid ester (melting point, 29-30°C).

Latest revision as of 05:00, 5 October 2010

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Upper classes: LB LBF



(9E,12E,15E) -Octadecatrienoic acid
LBF18303SC02.png
Structural Information
(trans-9,trans-12,trans-15) -Octadecatrienoic acid
  • (9E,12E,15E) -Octadecatrienoic acid
  • Elaidolinoleic acid
C18:3
Formula C18H30O2
Exact Mass 278.224580204
Average Mass 278.4296
SMILES CCC=CCC=CCC=CCCCCCCCC(O)=O
Physicochemical Information
29.5-30°C
solubule in methyl alcohol and petroleum ether. Kass_JP et al.
Synthetic, by treatment of the ester form of alpha -linolenic acid with 1% Se at 205-215°C to yield this acid ester (melting point, 29-30°C).
Spectral Information
Mass Spectra
UV Spectra
IR Spectra
NMR Spectra
Other Spectra
Chromatograms
Reported Metabolites, References
Biospecies ID Compound Name Reference Comment
n.a. LBF18303SC02 See above. Kass_JP et al. 1941