Some Analytical Observations of Autoxidation Products of Linoleic Acid and Their Thiobarbituric Acid Reactive Substances
- 9 September 1983
- journal article
- research article
- Published by Oxford University Press (OUP) in Agricultural and Biological Chemistry
- Vol. 47 (9) , 2035-2043
- https://doi.org/10.1080/00021369.1983.10865903
Abstract
Autoxidation products of linoleic acid (LA) were analyzed, when the weight became 1.14-fold under the autoxidation conditions of satisfactory atmospheric oxygen, at 37°C, in the dark, for 7 days. The LA absorbed 2.8 mol of oxygen to form secondary degradation products. This autoxidized LA consisted of 45% intact substance, 22% a mixture of polymers and endoperoxides, 18% LA hydroperoxides, 3% polar products, 1.7% azelaldehydeic acid, 1.3% hexahal, 0.9% azelaic acid, 0.6% octanoic acid, 0.3% suberaldehydeic acid, and so on. Thus, unstable 2,4-dienoic carbonyls were the main intermediate products of autoxidation of LA. Therefore, malonaldehyde was not a main product nor a major thiobarbituric acid reactive substance.This publication has 2 references indexed in Scilit:
- Lack of regioselectivity in formation of oxohydroxyoctadecenoic acids from the 9‐ or 13‐hydroperoxide of linoleic acidLipids, 1979
- Mass Spectrometry of Long-Chain EstersPublished by Elsevier ,1963