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D-Glucitol, also known as 6-O-R-D-galactopyranosyl, is a naturally occurring sugar alcohol derived from D-glucose. It is a polyol, which means it has multiple hydroxyl groups, and is often used as a sweetener in food products due to its low glycemic index and reduced calorie content compared to sugar. D-Glucitol,6-O-R-D-galactopyranosyl- is also known for its humectant properties, making it useful in pharmaceuticals and cosmetics to retain moisture. In the chemical structure, the 6-O-R-D-galactopyranosyl refers to the specific glycosidic linkage where a galactose molecule is attached to the sixth carbon of the glucitol molecule, forming a disaccharide. This particular chemical structure is significant in the field of carbohydrate chemistry and biochemistry, as it can influence the compound's biological activity and applications in various industries.

497-83-6

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497-83-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 497-83-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,9 and 7 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 497-83:
(5*4)+(4*9)+(3*7)+(2*8)+(1*3)=96
96 % 10 = 6
So 497-83-6 is a valid CAS Registry Number.

497-83-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name α-D-Galp-(1->6)-D-Glc-ol

1.2 Other means of identification

Product number -
Other names (2S,3R,4R,5R)-6-((2S,3R,4S,5R,6R)-3,4,5-Trihydroxy-6-hydroxymethyl-tetrahydro-pyran-2-yloxy)-hexane-1,2,3,4,5-pentaol

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:497-83-6 SDS

497-83-6Downstream Products

497-83-6Relevant academic research and scientific papers

SELECTIVE DEGRADATION OF THE GLYCOSYLURONIC ACID RESIDUES OF COMPLEX CARBOHYDRATES BY LITHIUM DISSOLVED IN ETHYLENEDIAMINE

Lau, James M.,McNeil, Michael,Darvill, Alan G.,Albersheim, Peter

, p. 219 - 244 (2007/10/02)

Lithium metal dissolved in ethylenediamine had been demonstrated to cleave a 3-linked glycosyluronic acid-containing polysaccharide .The present study with model compounds has established that, by lithium treatment, carbohydrates are cleaved at the sites of the glycosyluronic acid residues, regerdless of the point at which other glycosyl residues are attached to the glycosyluronic acid residue.Treatment of carbohydrates with lithium metal dissolved in ethylenediamine also results in cleavage of methyl glycosides, reduction of aldoses, and cleavage of methyl ethers and pyruvic acetals of glycosyl residues.Model compounds were used to demonstrate that oligosaccharides containing only neutral glycosyl residues are largely stable to the reaction conditions (except for the reduction of the glycose residue of each oligosaccharide).Thus, a general procedure for the selective cleavage of underivatized carbohydrates at the glycosyluronic acid residues is described.

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