LBF18206HP03
From Jcbl.jp
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Fatty acid (脂肪酸) |
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IDs and Links | |
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LipidBank | |
DFA8004 | |
LipidMaps | |
LMFA01040007 | |
CAS | |
KEGG | |
{{{KEGG}}} | |
KNApSAcK | |
LBF18206HP03.mol |
12-Hydroperoxy-9,13-octadecadienoate | |
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Structural Information | |
Systematic Name | 12-Hydroperoxy-9,13-octadecadienoic acid |
Common Name |
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Symbol | |
Formula | C18H32O4 |
Exact Mass | 312.23005951199997 |
Average Mass | 312.44428 |
SMILES | CCCCC=CC(OO)CC=CCCCCCCCC(O)=O |
Physicochemical Information | |
Melting Point | |
Boiling Point | |
Density | |
Optical Rotation | |
Refractive Index | |
Solubility | |
Source | Oxidation of methyl linoleate by singlet oxygen Frankel_EN Frankel_EN Frankel_EN Frankel_EN . |
Chemical Synthesis | |
Metabolism | |
Biological Activity | Pysiological damages are induced by these hydroperoxides which are incorporated into bodies or synthesized endogenously. Logani_MK et al. Sevanian_A et al. Fujimoto_K |
Genetic Information | |
Note | |
Spectral Information | |
Mass Spectra | GC-EI-MS(after methanolysis, reduction and trimethylsilylation) TeraoJet al. Frankel_EN et al.: m/e= 185[SMTO=CH-CH=CH-(CH2)3CH3], GC-EI-MS (after methylation, reduction and hydrogenation) Chan_HWS : m/e= 229[CH(OH)(CH2)10COOCH3], 200[(CH2)10COOCH3+H], 197[C(OH)(CH2)10CO] GC-EI-MS(after methylation, reduction, hydrogenation and trimethylsilylation) TeraoJet al. |
UV Spectra | |
IR Spectra | After methanolyzation and reduction Thomas_MJ et al. TeraoJet al.: isolated double bond (3013-3010, 972-971cm-1) |
NMR Spectra | 1H-NMR(after methanolyzation and reduction) Thomas_MJ et al.: olefinic protons(5.55-5.59ppm), C10 (4.08-4.11ppm) |
Other Spectra | |
Chromatograms |
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