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10003-64-2

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10003-64-2 Usage

Chemical Properties

Off-White Solid

Uses

An Amadori compound having the potential to alter cellular adhesion, inhibit cancer metastasis and induce apoptosis.

Check Digit Verification of cas no

The CAS Registry Mumber 10003-64-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,0,0 and 3 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 10003-64:
(7*1)+(6*0)+(5*0)+(4*0)+(3*3)+(2*6)+(1*4)=32
32 % 10 = 2
So 10003-64-2 is a valid CAS Registry Number.

10003-64-2SDS

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 (2R)-3-methyl-2-[[(3S,4R,5R)-2,3,4,5-tetrahydroxyoxan-2-yl]methylamino]butanoic acid

1.2 Other means of identification

Product number -
Other names 1-Deoxy-1-L-valino-D-fructose

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:10003-64-2 SDS

10003-64-2Relevant articles and documents

Analysis of Amadori compounds by high-performance cation exchange chromatography coupled to tandem mass spectrometry

Davidek, Tomas,Kraehenbuehl, Karin,Devaud, Stephanie,Robert, Fabien,Blank, Imre

, p. 140 - 147 (2005)

High-performance cation exchange chromatography coupled to tandem mass spectrometry or electrochemical detection was found to be an efficient tool for analyzing Amadori compounds derived from hexose and pentose sugars. The method allows rapid separation and identification of Amadori compounds, while benefiting from the well-known advantages of mass spectrometry, such as specificity and sensitivity. Glucose- and xylose-derived Amadori compounds of several amino acids, such as glycine, alanine, valine, leucine/isoleucine, methionine, proline, phenylalanine, and glutamic acid, were separated or discriminated using this new method. The method is suitable for the analysis of both model reaction mixtures and food products. Fructosylglutamate was found to be the major Amadori compound in dried tomatoes (~1.5 g/100 g) and fructosylproline in dried apricots (~0.2 g/100 g). Reaction of xylose and glycine at 90 °C (pH 6) for 2 h showed rapid formation of xylulosylglycine (~12 mol %, 15 min) followed by slow decrease over time. Analysis of pentose-derived Amadori compounds is shown for the first time, which represents a major breakthrough in studying occurrence, formation, and decomposition of these labile Maillard intermediates.

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