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10003-64-2

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10003-64-2 Usage

Description

Fructosylvaline, an Amadori compound, is an off-white solid with the potential to alter cellular adhesion, inhibit cancer metastasis, and induce apoptosis. It is a derivative of hydrolyzable tannins and possesses unique chemical properties that make it a promising candidate for various applications in different industries.

Uses

Used in Pharmaceutical Industry:
Fructosylvaline is used as a pharmaceutical agent for its ability to alter cellular adhesion, which can help in inhibiting cancer metastasis and inducing apoptosis. Its unique properties make it a valuable compound in the development of new drugs and therapies for cancer treatment.
Used in Cosmetics Industry:
Fructosylvaline is used as an ingredient in the cosmetics industry for its potential to improve skin health and appearance. Its ability to alter cellular adhesion may contribute to the development of products that promote skin regeneration and repair.
Used in Food Industry:
Fructosylvaline is used as an additive in the food industry due to its off-white solid form and unique chemical properties. It may be utilized to enhance the texture, flavor, or shelf life of certain food products.
Used in Research and Development:
Fructosylvaline is used as a research compound for its potential applications in various fields, including pharmaceuticals, cosmetics, and the food industry. Its unique properties make it an interesting subject for further study and development of new products and therapies.

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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