LBF18304SC02: Difference between revisions

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|Solubility=[[Reference:Kass_JP:Miller_ES:Burr_GO:,J. Am. Chem. Soc.,1939,61,482|{{RelationTable/GetFirstAuthor|Reference:Kass_JP:Miller_ES:Burr_GO:,J. Am. Chem. Soc.,1939,61,482}}]]
|Solubility=[[Reference:Kass_JP:Miller_ES:Burr_GO:,J. Am. Chem. Soc.,1939,61,482|{{RelationTable/GetFirstAuthor|Reference:Kass_JP:Miller_ES:Burr_GO:,J. Am. Chem. Soc.,1939,61,482}}]]
|Source=
|Source=
|Chemical Synthesis=Synthetic, by isomerization of <FONT FACE="Symbol">a</FONT>-linolenic acid.
|Chemical Synthesis=Synthetic, by isomerization of alpha -linolenic acid.
|Metabolism=
|Metabolism=
|Symbol=C18:3
}}
}}


{{Lipid/Footer}}
{{Lipid/Footer}}

Latest revision as of 21:00, 14 April 2010

LipidBank Top
(トップ)
Fatty acid
(脂肪酸)
Glycerolipid
(グリセロ脂質)
Sphingolipid
(スフィンゴ脂質)
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Upper classes: LB LBF



9, 12, 14-Octadecatrienoic acid
LBF18304SC02.png
Structural Information
9, 12, 14-Octadecatrienoic acid
  • 9, 12, 14-Octadecatrienoic acid
C18:3
Formula C18H30O2
Exact Mass 278.224580204
Average Mass 278.4296
SMILES CCCC=CC=CCC=CCCCCCCCC(O)=O
Physicochemical Information
Kass_JP et al.
Synthetic, by isomerization of alpha -linolenic acid.
Spectral Information
Mass Spectra
UV Spectra
IR Spectra
NMR Spectra
Other Spectra
Chromatograms
Reported Metabolites, References
Biospecies ID Compound Name Reference Comment
n.a. LBF18304SC02 See above. Kass_JP et al. 1939