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1-O,2-O,3-O,4-O-Tetrakis(trimethylsilyl)-D-threitol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

32381-52-5

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32381-52-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 32381-52-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,3,8 and 1 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 32381-52:
(7*3)+(6*2)+(5*3)+(4*8)+(3*1)+(2*5)+(1*2)=95
95 % 10 = 5
So 32381-52-5 is a valid CAS Registry Number.

32381-52-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name trimethylsilyl ether of threitol

1.2 Other means of identification

Product number -
Other names (2R,3R)-1,2,3,4-Tetrakis-trimethylsilanyloxy-butane

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:32381-52-5 SDS

32381-52-5Downstream Products

32381-52-5Relevant academic research and scientific papers

Capillary gas-chromatographic analysis of monosaccharides: Improvements and comparisons using trifluoroacetylation and trimethylsilylation of sugar O-benzyl- and O-methyl-oximes

Andrews, Mark A.

, p. 1 - 19 (2007/10/02)

Two new procedures for the gas-chromatographic analysis of monosaccharides are reported. One involves derivatization of the sugars by reaction with O-benzylhydroxylamine followed by trifluoroacetylation with N-methylbis(trifluoroacetamide) and chromatography on a DB-1701 capillary column. This technique probably provides the best resolution achieved to date of the C3-C6 aldoses, as well as of the corresponding alditols. Ketoses can be qualitatively analyzed by this method, but complications interfere with their quantitative analysis. The second procedure also involves initial derivatization as the O-benzyloxime, but is followed by trimethylsilylation with 1-trimethylsilylimidazole, and chromatography on a DB-17 column. This technique is particularly useful for C5 sugars, C6 ketoses, and mixtures of sugars, alditols, and/or lactones. A number of additional, critical, observations on the derivatization and capillary gas-chromatographic analysis of monosaccharides are described.

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