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A detailed identification study on high-temperature degradation products of oleic and linoleic acid methyl esters by GC-MS and GC-FTIR
Authors:Berdeaux Olivier  Fontagné Stéphanie  Sémon Etienne  Velasco Joaquin  Sébédio Jean Louis  Dobarganes Carmen
Institution:1. Plate-forme ChemoSens, Centre des Sciences du Goût et de l’Alimentation, UMR6265 CNRS, UMR1324 INRA, Université de Bourgogne, Agrosup Dijon, 21000 Dijon, France;2. UR1067 INRA, Nutrition, Métabolisme, Aquaculture, 64310 Saint-Pée-sur-Nivelle, France;3. Instituto de la Grasa (CISC), Avda. Padre García Tejero 4, 41012 Seville, Spain;4. UMR 1019, INRA-Université d’Auvergne, Plate-forme d’exploration du métabolisme, des gènes aux métabolites, 63122 St Genès Champanelle, France
Abstract:GC-MS and GC-FTIR were complementarily applied to identify oxidation compounds formed under frying conditions in methyl oleate and linoleate heated at 180°C. 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.
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