Comparison of Methylation Procedures for Conjugated Linoleic Acid and Artifact Formation by Commercial (Trimethylsilyl)diazomethane
- 15 February 2001
- journal article
- research article
- Published by American Chemical Society (ACS) in Journal of Agricultural and Food Chemistry
- Vol. 49 (3), 1158-1164
- https://doi.org/10.1021/jf001209z
Abstract
Four different methods for methylating conjugated linoleic acid (CLA) were compared. The HCl/MeOH and BF3/MeOH methods were tested under different time and temperature combinations. Increasing temperature and/or incubation time for either method decreased the cis-9,trans-11 and trans-10,cis-12 isomers, but trans-9,trans-11/trans-10,trans-12 isomers and artifacts (allylic methoxide) were increased. In addition, the triacylglyceride form of CLA was tested using the above methods and NaOMe at various temperatures for 20 min. The NaOMe did not generate methoxy artifacts. However, there were impurities in GC after methylation with NaOMe as well as with BF3/MeOH. The (trimethylsilyl)diazomethane method, which is a mild and easy alternative, was tested. Free forms of fatty acids were easily, but not completely, methylated by this method. Also, the method generated artifacts (trimethylsilyl CLA esters) and impurities (trimethylsilyl) that would interfere with short-chain fatty-acid analysis by GC. Keywords: Conjugated linoleic acid; CLA; methylation; (trimethylsilyl)diazomethane.Keywords
This publication has 4 references indexed in Scilit:
- Mechanisms of Action of Conjugated Linoleic Acid: Evidence and SpeculationProceedings of the Society for Experimental Biology and Medicine, 2000
- Evidence that commercial calf and horse sera can contain substantial amounts of trans‐10,cis‐12 conjugated linoleic acidLipids, 1998
- Biohydrogenation of Unsaturated Fatty AcidsJournal of Biological Chemistry, 1967
- The Use Of Trifluoroacetic Anhydride And Related Compounds In Organic SynthesesChemical Reviews, 1955