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Preparation of fatty acid methyl esters for gas-liquid chromatography

Journal of Lipid Research · 2009 · Vol. 51(3) · pp. 635–640
K. IchiharaYumeto Fukubayashi

Abstract

A convenient method using commercial aqueous concentrated HCl (conc. HCl; 35%, w/w) as an acid catalyst was developed for preparation of fatty acid methyl esters (FAMEs) from sterol esters, triacylglycerols, phospholipids, and FFAs for gas-liquid chromatography (GC). An 8% (w/v) solution of HCl in methanol/water (85:15, v/v) was prepared by diluting 9.7 ml of conc. HCl with 41.5 ml of methanol. Toluene (0.2 ml), methanol (1.5 ml), and the 8% HCl solution (0.3 ml) were added sequentially to the lipid sample. The final HCl concentration was 1.2% (w/v). This solution (2 ml) was incubated at 45 degrees C overnight or heated at 100 degrees C for 1-1.5 h. The amount of FFA formed in the presence of water derived from conc. HCl was estimated to be <1.4%. The yields of FAMEs were >96% for the above lipid classes and were the same as or better than those obtained by saponification/methylation or by acid-catalyzed methanolysis/methylation using commercial anhydrous HCl/methanol. The method developed here could be successfully applied to fatty acid analysis of various lipid samples, including fish oils, vegetable oils, and blood lipids by GC.

Analytical Chemistry and ChromatographyFatty Acid Research and HealthBiochemical Analysis and Sensing TechniquesChemistrySaponificationMethanolChromatographyAnhydrousGas chromatographyFatty acidFatty acid methyl esterTolueneAqueous solution

MeSH terms

MethanolChromatography, LiquidEstersFatty AcidsFish OilsHydrochloric AcidIndicators and ReagentsKineticsLipidsMethylationPlant OilsSolubilityTemperatureTolueneWater
Citations
640
FWCI
3.32
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24
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92%
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References
Direct transesterification of all classes of lipids in a one-step reaction.
Journal of Lipid Research · 1986 · 2,380 citations
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