1978
DOI: 10.1093/chromsci/16.8.329
|View full text |Cite
|
Sign up to set email alerts
|

A Novel and Rapid Method for the Preparation of Methyl Esters for Gas Chromatography: Application to the Determination of the Fatty Acids of Edible Fats and Oils

Abstract: A rapid, mild, and convenient transesterification of triglycerides was obtained using 0.2 N-methanolic (m-trifluoro-methylphenyl) trimethylammonium hydroxide. The method yielded results comparable to those obtained using methanolic sodium methoxide.

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1
1

Citation Types

0
21
0

Year Published

1980
1980
2016
2016

Publication Types

Select...
9

Relationship

0
9

Authors

Journals

citations
Cited by 64 publications
(21 citation statements)
references
References 0 publications
0
21
0
Order By: Relevance
“…In this case, the carboxylic end of the resulting fragment is converted to an alkoxycarbonyl group whereas the hydroxyl remains unchanged: 3 A further class of alkylating reagents, comprising tetramethylammonium hydroxide (TMAH), trimethylanilinium hydroxide and trimethylsulfonium hydroxide provides an efficient transformation of carboxylic acids into methyl esters under thermal conditions. [23][24][25][26][27][28][29] The reaction can be accomplished in a sealed tube at 300°C 30 or, most conveniently, on-line in the flash heater of a gas chromatograph at 250-300°C or even in a Curie-point pyrolyzer connected to a gas chromatograph/mass spectrometer:…”
Section: Diazomethane Is Usually Prepared By Reaction Of Nitrosomethymentioning
confidence: 99%
“…In this case, the carboxylic end of the resulting fragment is converted to an alkoxycarbonyl group whereas the hydroxyl remains unchanged: 3 A further class of alkylating reagents, comprising tetramethylammonium hydroxide (TMAH), trimethylanilinium hydroxide and trimethylsulfonium hydroxide provides an efficient transformation of carboxylic acids into methyl esters under thermal conditions. [23][24][25][26][27][28][29] The reaction can be accomplished in a sealed tube at 300°C 30 or, most conveniently, on-line in the flash heater of a gas chromatograph at 250-300°C or even in a Curie-point pyrolyzer connected to a gas chromatograph/mass spectrometer:…”
Section: Diazomethane Is Usually Prepared By Reaction Of Nitrosomethymentioning
confidence: 99%
“…16 Analysis of platelet fatty acids was performed by gas chromatography using an HP Model 5700 gas chromatograph (Hewlett-Packard, Palo Alto, Calif.) equipped with a flame ionization detector, a 50-mx 0.53-mm capillary column isothermal at 250°C, and a flow rate of N 2 of 10 ml/min. This approach permits quantification of fatty acid methyl esters with 16 and more carbon atoms.…”
Section: Platelet Fatty Acid Compositionmentioning
confidence: 99%
“…The fat from the surface layer was removed using a Pasteur pipette, stored at −20 °C, and solubilized in dichloromethane (1:9). The methyl esters were formed according to the method of McCreary, et al (1978) and quantified by gas chromatography (GC).…”
Section: Methodsmentioning
confidence: 99%