Two methods are described for locating the 0- (carboxymethyl) groups in O-(carboxymethyl)guar. In Method I, 0-(carboxymethyl)guar was depolymerized by methanolysis, the 0-(carboxymethyl) groups were reduced, and the mixture of methyl glycosides and 0-(2-hydroxyethyl)-substituted methyl glycosides wa
A quantitative method to determine the points of O-(2-hydroxypropyl) substitution in O-(2-hydroxypropyl)-guar
β Scribed by Michael McNeil; Peter Albersheim
- Publisher
- Elsevier Science
- Year
- 1984
- Tongue
- English
- Weight
- 410 KB
- Volume
- 131
- Category
- Article
- ISSN
- 0008-6215
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β¦ Synopsis
A method is described for locating the 0-(2-hydroxypropyl) groups in 0-(2hydroxypropyl)-substituted guar.
Per-0-methylation of the O-(Zhydroxypropyl)guar yielded guar that was partially 0-methylated and partially 0-(2methoxypropyl)ated.
This polymer was hydrolyzed, to afford a mixture of partially 0-methylated monosaccharides and partially 0-(2-methoxypropylated), partially 0-methylated monosaccharides. These monosaccharide derivatives were reduced, and the alditols acetylated, to give a mixture of partially 0-acetylated, partially Omethylated alditols with partially 0-acetylated, partially O-(Zmethoxypropyl)ated, partially 0-methylated alditols. These alditol derivatives were identified by gas-liquid chromatography-mass spectrometry, and quantitated by gasliquid chromatography.
π SIMILAR VOLUMES
Samples of O-(2-hydroxypropyl)derivatives of cyclomaltoheptaose (beta-cyclodextrin) with increasing substitution were prepared by withdrawing aliquots at different times from a reaction mixture containing cyclomaltoheptaose and an excess of (S)-propylene oxide in 0.39 M aqueous sodium hydroxide. The