LBF16304SC01

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Upper classes: LB LBF



6, 9, 12-Hexadecatrienoic acid
LBF16304SC01.png
Structural Information
Systematic Name 6, 9, 12-Hexadecatrienoic acid
Common Name
  • 6, 9, 12-Hexadecatrienoic acid
Symbol C16:3
Formula C16H26O2
Exact Mass 250.19328007599998
Average Mass 250.37643999999997
SMILES CCCC=CCC=CCC=CCCCCC(O)=O
Physicochemical Information
Melting Point
Boiling Point
Density
Optical Rotation
Refractive Index
Solubility soluble in alcohol and ether. KlenkEet al. StoffelWet al. StoffelWet al.
Source Herring, menhaden and rapeseed oils. Muscle lipids and internal lipids in a sardine. ( The concentration of internal lipids in total fatty acid is higher than that of muscle lipids. ) Hayashi_A et al.
Chemical Synthesis
Metabolism
Biological Activity
Genetic Information
Note
Spectral Information
Mass Spectra HR-EI-MS (METHYL ESTER) : M/Z; 264.20910(M) 001) EI-MS (PYRROLIDIDE) : M/Z; 154, 166, 194, 206, 234, 246 HayashiAet al..
UV Spectra
IR Spectra
NMR Spectra CMR (METHYL ESTER) : C12, 127.797; C13, 130.127; C14, 29.308; C15, 22.753; C16: 13.760ppm HayashiAet al. PMR(METHYL ESTER): CH3-C-C-C=C- (TERMINAL METHYL GROUP) , 0.83-0.98ppm (TRIPLETS) HayashiAet al.
Other Spectra
Chromatograms
Reported Metabolites, References
Biospecies ID Compound Name Reference Comment
n.a. LBF16304SC01 See above. Hayashi_A et al. 1970
n.a. LBF16304SC01 See above. Klenk_E et al. 1959
n.a. LBF16304SC01 See above. Stoffel_W et al. 1959
n.a. LBF16304SC01 See above. Stoffel_W et al. 1958


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