LBF18207HP02: Difference between revisions

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|IR Spectra=Ester carbonyl(1740cm<SUP><FONT SIZE=-1>-</FONT></SUP><SUP><FONT SIZE=-1>1</FONT></SUP>), trans, trans diene(991cm<SUP><FONT SIZE=-1>-</FONT></SUP><SUP><FONT SIZE=-1>1</FONT></SUP>)[[Reference:Schieberle_P:Grosch_W:,Z. Lebensm. Unters. Forsch.,1981,173,192|{{RelationTable/GetFirstAuthor|Reference:Schieberle_P:Grosch_W:,Z. Lebensm. Unters. Forsch.,1981,173,192}}]]
|IR Spectra=Ester carbonyl(1740cm<SUP><FONT SIZE=-1>-</FONT></SUP><SUP><FONT SIZE=-1>1</FONT></SUP>), trans, trans diene(991cm<SUP><FONT SIZE=-1>-</FONT></SUP><SUP><FONT SIZE=-1>1</FONT></SUP>)[[Reference:Schieberle_P:Grosch_W:,Z. Lebensm. Unters. Forsch.,1981,173,192|{{RelationTable/GetFirstAuthor|Reference:Schieberle_P:Grosch_W:,Z. Lebensm. Unters. Forsch.,1981,173,192}}]]
|NMR Spectra=<SUP><FONT SIZE=-1>1</FONT></SUP>H-NMR[[Reference:Schieberle_P:Grosch_W:,Z. Lebensm. Unters. Forsch.,1981,173,192|{{RelationTable/GetFirstAuthor|Reference:Schieberle_P:Grosch_W:,Z. Lebensm. Unters. Forsch.,1981,173,192}}]]: C9-C12(5.5-6.1ppm), C13(4.1ppm), C8(2.1ppm)
|NMR Spectra=<SUP><FONT SIZE=-1>1</FONT></SUP>H-NMR[[Reference:Schieberle_P:Grosch_W:,Z. Lebensm. Unters. Forsch.,1981,173,192|{{RelationTable/GetFirstAuthor|Reference:Schieberle_P:Grosch_W:,Z. Lebensm. Unters. Forsch.,1981,173,192}}]]: C9-C12(5.5-6.1ppm), C13(4.1ppm), C8(2.1ppm)
|Source=A degradation product of 13-hydroperoxymethyllinoleate in the presence of di-tert-butyl peroxyoxalate[[Reference:Schieberle_P:Grosch_W:,Z. Lebensm. Unters. Forsch.,1981,173,192|{{RelationTable/GetFirstAuthor|Reference:Schieberle_P:Grosch_W:,Z. Lebensm. Unters. Forsch.,1981,173,192}}]];>.
|Chemical Synthesis=
|Metabolism=
}}
}}


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Revision as of 22:00, 24 November 2009

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Upper classes: LB LBF



Methyl 13-Butylperoxy-9,11-Octadecadienoate
LBF18207HP02.png
Structural Information
Methyl 13-Butylperoxy-9,11-Octadecadienoate
  • Methyl 13-Butylperoxy-9,11-Octadecadienoate
Formula C23H42O4
Exact Mass 382.30830983199996
Average Mass 382.57718
SMILES C(C)CCCC(OOC(C)(C)C)C=CC=CCCCCCCCC(=O)OC
Physicochemical Information
A degradation product of 13-hydroperoxymethyllinoleate in the presence of di-tert-butyl peroxyoxalate Schieberle_P et al.;>.
Spectral Information
Mass Spectra GC-EI-MS(hydrogenation with palladium-charcoal) SchieberlePet al.
UV Spectra lether/max=234nm SchieberlePet al.
IR Spectra Ester carbonyl(1740cm-1), trans, trans diene(991cm-1) SchieberlePet al.
NMR Spectra 1H-NMR SchieberlePet al.: C9-C12(5.5-6.1ppm), C13(4.1ppm), C8(2.1ppm)
Other Spectra
Chromatograms
Reported Metabolites, References
Biospecies ID Compound Name Reference Comment
n.a. LBF18207HP02 See above. Schieberle_P et al. 1981