2010
DOI: 10.1194/jlr.d001065
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Preparation of fatty acid methyl esters for gas-liquid chromatography

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Cited by 529 publications
(384 citation statements)
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“…After that lipid extracts were separated by thinlayer chromatography in the system of solvents hexan : diethyl ether : glacial acetic acid (85 : 15 : 1) a fraction of free fatty acids was methylated with 3 М HCl in methanol [12].…”
Section: Methodsmentioning
confidence: 99%
“…After that lipid extracts were separated by thinlayer chromatography in the system of solvents hexan : diethyl ether : glacial acetic acid (85 : 15 : 1) a fraction of free fatty acids was methylated with 3 М HCl in methanol [12].…”
Section: Methodsmentioning
confidence: 99%
“…Transesterification with these reagents can be developed at room temperature in a short period of time. On the other hand, a disadvantage is that they do not convert free fatty acids in FAME, which limit its application to oils with high acidity (Simionato et al, 2010;Ichihara and Fukubayashi, 2010).…”
Section: Preparation Of Fatty Acid Methyl Esters (Fame)mentioning
confidence: 99%
“…Transesterification with these reagents can be developed at room temperature in a short period of time. On the other hand, a disadvantage is that they do not convert free fatty acids in FAME, which limit its application to oils with high acidity (Simionato et al, 2010;Ichihara and Fukubayashi, 2010). For the analysis of CLA in samples having high levels of free fatty acids, Kramer et al (1997) reported a method using acid and base catalysis in sequence.…”
Section: Ajabsmentioning
confidence: 99%
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