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Journal ArticleDOI

Gas-Liquid Chromatographic Separation of Partially and Fully Methylated Methyl Glucopyranosides

W. John Lewicki, +1 more
- 01 Mar 1970 - 
- Vol. 3, Iss: 3, pp 151-157
TLDR
This article showed that the absence of a C6 methoxyl group lowers the response of a flame ionization detector, and that the presence of C6 methyl glucopyranosides lowers the detection performance.
Abstract
Carbowax 20M treated with 2-nitroterephthalic acid used as the liquid phase for gas-liquid chromatography gives sharply resolved peaks for several partially and fully methylated methyl glucopyranosides. The detector response of the standard compounds shows that the absence of a C6 methoxyl group lowers the response of a flame ionization detector.

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Citations
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Book ChapterDOI

Applications of Gas-Liquid Chromatography to Carbohydrates :Part I°

TL;DR: In this paper, the authors discuss the application of trimethylsilyl derivatives of carbohydrates in gas-liquid chromatography and the use of this method in the analysis of plant materials.
Journal ArticleDOI

Determination of the structure of a broth dextran produced by a cariogenic streptococcus

TL;DR: The broth polysaccharide from the cariogenic bacterium Streptococcus mutans E49 has been shown by periodate oxidation and methylation studies to be a highly branched dextran and a modification of the sodium hydride-methyl iodide method of methylation is presented.
Journal ArticleDOI

Chromatography of monosaccharides and disaccharides

TL;DR: Chromatographic procedures for measuring monosaccharides and disaccharide are reviewed in this article, where the most significant developments of the last decade are the increasing use of open tubular columns and bonded-packings based on silica.
References
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Journal ArticleDOI

Studies on reactions relating to carbohydrates and polysaccharides: lxvii. synthesis of methylated glucose derivatives

TL;DR: The Haworth methylation technique has been modified to provide improved methods of synthesis of 2,3-dimethyl-α- and β-methyl glucosides and 2, 3,4,6-tetramethyl glucose from glucose.
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