LBF18206HP03

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Upper classes: LB LBF



12-Hydroperoxy-9,13-Octadecadienoic Acid
LBF18206HP03.png
Structural Information
12-Hydroperoxy-9,13-Octadecadienoic Acid/12-Hydroperoxy-9,13-Octadecadienoate
  • 12-Hydroperoxy-9,13-Octadecadienoic Acid
  • 12-Hydroperoxy-9,13-Octadecadienoate
Formula C18H32O4
Exact Mass 312.23005951199997
Average Mass 312.44428
SMILES CCCCC=CC(OO)CC=CCCCCCCCC(O)=O
Physicochemical Information
Oxidation of methyl linoleate by singlet oxygen Frankel_EN Frankel_EN Frankel_EN Frankel_EN ;>.
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
Reported Metabolites, References
Biospecies ID Compound Name Reference Comment
n.a. LBF18206HP03 See above. Chan_HWS 1977
n.a. LBF18206HP03 See above. Frankel_EN 1987
n.a. LBF18206HP03 See above. Frankel_EN 1980
n.a. LBF18206HP03 See above. Frankel_EN 1983
n.a. LBF18206HP03 See above. Frankel_EN 1984
n.a. LBF18206HP03 See above. Frankel_EN et al. 1979
n.a. LBF18206HP03 See above. Fujimoto_K 1986
n.a. LBF18206HP03 See above. Logani_MK et al. 1980
n.a. LBF18206HP03 See above. Sevanian_A et al. 1985
n.a. LBF18206HP03 See above. Terao_J et al. 1977
n.a. LBF18206HP03 See above. Thomas_MJ et al. 1980