Application of Transesterification Derivatization Reaction for GC-MS Analysis

Authors

  • Adam Březina Department of Chemistry, Faculty of Science, Masaryk University, Brno, Czech Republic
  • Adéla Dořmanová Department of Chemistry, Faculty of Science, Masaryk University, Brno, Czech Republic
  • Petr Kukučka RECETOX, Faculty of Science, Masaryk University, Brno, Czech Republic
  • Přemysl Lubal Department of Chemistry, Faculty of Science, Masaryk University, Brno, Czech Republic
  • Marta Farková Department of Chemistry, Faculty of Science, Masaryk University, Brno, Czech Republic

DOI:

https://doi.org/10.54779/ccsss20220319

Keywords:

derivatization, GC-MS, lipids, oils, transesterification

Abstract

This paper is focused on study of the concentration of the basic catalyst in methanol on the yield of the derivatization transesterification reaction of triacyglycerols. Potassium hydroxide and sodium hydroxide solutions were used as basic catalysts. Triacylglycerols were transesterified, rapeseed oil was used as a sample. Triacylglycerols were converted to methyl esters of fatty acids, which were subsequently determined by GC-MS where the peak areas were monitored, because they represent the yield of the formed fatty acid methyl esters, namely palmitic, oleic, linoleic and stearic acids. The highest yield of transesterification of the oil to methylesters of fatty acids was found for a concentration of 3.0 mol dm–3 for KOH and 2.0 mol dm–3 for NaOH. At higher catalyst concentrations, a predominant side-reaction, saponification, was observed, which decreased the overall yield of fatty acid methyl esters.

Published

2022-11-02