LBF16304SC01

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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

IDs and Links
LipidBank	DFA0175
LipidMaps	LMFA01030136
CAS
KEGG	{{{KEGG}}}
KNApSAcK	{{{KNApSAcK}}}
mol	LBF16304SC01

6, 9, 12-Hexadecatrienoic acid
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