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Galactosylisomaltol is a glycosylation end product that is formed through the Maillard reaction of lactose via the 1-deoxyosone pathway. It is a naturally occurring compound that can be found in commercial drinking milk.

82756-28-3

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82756-28-3 Usage

Uses

Used in Food Industry:
Galactosylisomaltol is used as a natural compound in the food industry, specifically in commercial drinking milk. Its presence in milk is a result of the Maillard reaction, which contributes to the flavor and aroma of the product.

Check Digit Verification of cas no

The CAS Registry Mumber 82756-28-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,7,5 and 6 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 82756-28:
(7*8)+(6*2)+(5*7)+(4*5)+(3*6)+(2*2)+(1*8)=153
153 % 10 = 3
So 82756-28-3 is a valid CAS Registry Number.

82756-28-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name galactosyl isomaltol

1.2 Other means of identification

Product number -
Other names 3-O-β-D-galactopyranosyloxy-2-furyl methyl ketone

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:82756-28-3 SDS

82756-28-3Relevant academic research and scientific papers

Efficient syntheses of N-alkyl-3-hydroxy-2-methyl-4(1H)-pyridinones from carbohydrate precursors

Fox, Raymond C.,Taylor, Paul D.

, p. 989 - 1001 (1999)

N-alkyl-3-hydroxy-2-methyl-4(1H)-pyridinones can be synthesised in reasonable yield from either 1-(3-hydroxy-2-furanyl)ethanone or O- galactosylisomaltol. Since these carbohydrate precursors can be produced from the disaccharide, α-D-lactose, a simple and inexpensive transformation into pyridinones is possible.

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