LBF16304SC01: Difference between revisions
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|LipidMaps=LMFA01030136 | |LipidMaps=LMFA01030136 | ||
|SysName=6, 9, 12-Hexadecatrienoic acid | |SysName=6, 9, 12-Hexadecatrienoic acid | ||
|Common Name=&&6, 9, 12-Hexadecatrienoic acid&& | |||
|Solubility=soluble in alcohol and ether.[[Reference:Klenk_E:Steinbach_H:,Hoppe Seylers Z. Physiol. Chem.,1959,316,31|{{RelationTable/GetFirstAuthor|Reference:Klenk_E:Steinbach_H:,Hoppe Seylers Z. Physiol. Chem.,1959,316,31}}]][[Reference:Stoffel_W:Ahrens_EH_Jr:,J. Am. Chem. Soc.,1958,80,6604|{{RelationTable/GetFirstAuthor|Reference:Stoffel_W:Ahrens_EH_Jr:,J. Am. Chem. Soc.,1958,80,6604}}]][[Reference:Stoffel_W:Ahrens_EH_Jr:,J. Lipid Res.,1959,1,139|{{RelationTable/GetFirstAuthor|Reference:Stoffel_W:Ahrens_EH_Jr:,J. Lipid Res.,1959,1,139}}]] | |Solubility=soluble in alcohol and ether.[[Reference:Klenk_E:Steinbach_H:,Hoppe Seylers Z. Physiol. Chem.,1959,316,31|{{RelationTable/GetFirstAuthor|Reference:Klenk_E:Steinbach_H:,Hoppe Seylers Z. Physiol. Chem.,1959,316,31}}]][[Reference:Stoffel_W:Ahrens_EH_Jr:,J. Am. Chem. Soc.,1958,80,6604|{{RelationTable/GetFirstAuthor|Reference:Stoffel_W:Ahrens_EH_Jr:,J. Am. Chem. Soc.,1958,80,6604}}]][[Reference:Stoffel_W:Ahrens_EH_Jr:,J. Lipid Res.,1959,1,139|{{RelationTable/GetFirstAuthor|Reference:Stoffel_W:Ahrens_EH_Jr:,J. Lipid Res.,1959,1,139}}]] | ||
|Mass Spectra=HR-EI-MS (METHYL ESTER) : M/Z; 264.20910(M) 001) EI-MS (PYRROLIDIDE) : M/Z; 154, 166, 194, 206, 234, 246[[Reference:Hayashi_A:Matsubara_T:,Biochim. Biophys. Acta,1970,202,228|{{RelationTable/GetFirstAuthor|Reference:Hayashi_A:Matsubara_T:,Biochim. Biophys. Acta,1970,202,228}}]]. | |Mass Spectra=HR-EI-MS (METHYL ESTER) : M/Z; 264.20910(M) 001) EI-MS (PYRROLIDIDE) : M/Z; 154, 166, 194, 206, 234, 246[[Reference:Hayashi_A:Matsubara_T:,Biochim. Biophys. Acta,1970,202,228|{{RelationTable/GetFirstAuthor|Reference:Hayashi_A:Matsubara_T:,Biochim. Biophys. Acta,1970,202,228}}]]. | ||
|NMR Spectra=CMR (METHYL ESTER) : C12, 127.797; C13, 130.127; C14, 29.308; C15, 22.753; C16: 13.760ppm [[Reference:Hayashi_A:Matsubara_T:,Biochim. Biophys. Acta,1970,202,228|{{RelationTable/GetFirstAuthor|Reference:Hayashi_A:Matsubara_T:,Biochim. Biophys. Acta,1970,202,228}}]] PMR(METHYL ESTER): CH3-C-C-C=C- (TERMINAL METHYL GROUP) , 0.83-0.98ppm (TRIPLETS) [[Reference:Hayashi_A:Matsubara_T:,Biochim. Biophys. Acta,1970,202,228|{{RelationTable/GetFirstAuthor|Reference:Hayashi_A:Matsubara_T:,Biochim. Biophys. Acta,1970,202,228}}]] | |NMR Spectra=CMR (METHYL ESTER) : C12, 127.797; C13, 130.127; C14, 29.308; C15, 22.753; C16: 13.760ppm [[Reference:Hayashi_A:Matsubara_T:,Biochim. Biophys. Acta,1970,202,228|{{RelationTable/GetFirstAuthor|Reference:Hayashi_A:Matsubara_T:,Biochim. Biophys. Acta,1970,202,228}}]] PMR(METHYL ESTER): CH3-C-C-C=C- (TERMINAL METHYL GROUP) , 0.83-0.98ppm (TRIPLETS) [[Reference:Hayashi_A:Matsubara_T:,Biochim. Biophys. Acta,1970,202,228|{{RelationTable/GetFirstAuthor|Reference:Hayashi_A:Matsubara_T:,Biochim. Biophys. Acta,1970,202,228}}]] | ||
}} | }} |
Revision as of 09:01, 20 December 2008
IDs and Links | |
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LipidBank | DFA0175 |
LipidMaps | LMFA01030136 |
CAS | |
KEGG | {{{KEGG}}} |
KNApSAcK | {{{KNApSAcK}}} |
mol | LBF16304SC01 |
6, 9, 12-Hexadecatrienoic acid | |
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Structural Information | |
6, 9, 12-Hexadecatrienoic acid | |
| |
Formula | C16H26O2 |
Exact Mass | 250.19328007599998 |
Average Mass | 250.37643999999997 |
SMILES | CCCC=CCC=CCC=CCCCCC(O)=O |
Physicochemical Information | |
soluble in alcohol and ether. KlenkEet al. StoffelWet al. StoffelWet al. | |
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 |
[hide]Reported Metabolites, References | |||||||||||||||||||||||||
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