6533b831fe1ef96bd1298fc5
RESEARCH PRODUCT
A detailed identification study on high-temperature degradation products of oleic and linoleic acid methyl esters by GC–MS and GC–FTIR
Olivier BerdeauxCarmen DobarganesJean Louis SébédioStéphanie FontagnéEtienne SémonJoaquín Velascosubject
030309 nutrition & dieteticsLinoleic acidMass-spectrometrychemistry.chemical_elementGas-chromatographyOleic AcidsBiochemistryGas Chromatography-Mass Spectrometry03 medical and health scienceschemistry.chemical_compound0404 agricultural biotechnologyFourier transform infraredFuranSpectroscopy Fourier Transform InfraredMoleculeOrganic chemistryMolecular BiologyBond cleavage0303 health sciencesAldehydesPrimary (chemistry)Organic ChemistryTemperaturePolar compounds04 agricultural and veterinary sciencesCell Biology040401 food scienceKeto AcidsThermoxidationShort-chain glycerol-bound compoundschemistryLinoleic AcidsGas chromatographyGas chromatography–mass spectrometryCarbon[SDV.AEN]Life Sciences [q-bio]/Food and Nutritiondescription
GC-MS and GC-FTIR were complementarily applied to identify oxidation compounds formed under frying conditions in methyl oleate and linoleate heated at 180ºC. The study was focused on the compounds that originated through hydroperoxide scission that remain attached to the glyceridic backbone in fats and oils and form part of non-volatile molecules. Twenty one short-chain esterified compounds, consisting of 8 aldehydes, 3 methyl ketones, 4 primary alcohols, 5 alkanes and 1 furan, were identified. In addition, twenty non-esterified volatile compounds, consisting of alcohols, aldehydes and acids, were also identified as major non-esterified components. Furanoid compounds of 18 carbon atoms formed by a different route were also identified in this study. Overall, the composition of the small fraction originated from hydroperoxide scission provides a clear idea of the complexity of the new compounds formed during thermoxidation and frying.
year | journal | country | edition | language |
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2012-04-01 |