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(2R,3R)-2,3-Dihydroxysuccinamide is a chiral organic compound with the molecular formula C4H6O4N2. It features a succinamide backbone with two hydroxyl groups attached, and it is known for its ability to form stable complexes with metal ions due to its chelating properties.

634-63-9

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634-63-9 Usage

Uses

Used in Chemical Processes:
(2R,3R)-2,3-Dihydroxysuccinamide is used as a chelating agent for its ability to bind metal ions, which is particularly useful in various industrial chemical processes. Its capacity to form stable complexes makes it a valuable component in these applications.
Used in Metal Coordination Chemistry:
In the field of metal coordination chemistry, (2R,3R)-2,3-Dihydroxysuccinamide is utilized as a chelating agent to create stable metal complexes. This property is crucial for research and development in this scientific domain.
Used in Pharmaceuticals:
(2R,3R)-2,3-Dihydroxysuccinamide is used as a reagent in the pharmaceutical industry, where its chelating ability can be harnessed for the development of new drugs and the improvement of existing ones.
Used in Water Treatment:
(2R,3R)-2,3-Dihydroxysuccinamide has potential applications in water treatment, where its metal-binding properties can be employed to remove or reduce metal ion concentrations in water systems.
Used as a Corrosion Inhibitor:
In industrial settings, (2R,3R)-2,3-Dihydroxysuccinamide can be used as a corrosion inhibitor. Its ability to bind with metal ions can help prevent or reduce corrosion on metal surfaces, which is beneficial for maintaining the integrity and longevity of metal structures and equipment.

Check Digit Verification of cas no

The CAS Registry Mumber 634-63-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,3 and 4 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 634-63:
(5*6)+(4*3)+(3*4)+(2*6)+(1*3)=69
69 % 10 = 9
So 634-63-9 is a valid CAS Registry Number.
InChI:InChI=1/C4H8N2O4/c5-3(9)1(7)2(8)4(6)10/h1-2,7-8H,(H2,5,9)(H2,6,10)

634-63-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3-Dihydroxybutanediamide

1.2 Other means of identification

Product number -
Other names -

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:634-63-9 SDS

634-63-9Relevant academic research and scientific papers

From single molecule to crystal: Mapping out the conformations of tartaric acids and their derivatives

Janiak, Agnieszka,Rychlewska, Urszula,Kwit, Marcin,Stepien, Urszula,Gawronska, Krystyna,Gawronski, Jacek

experimental part, p. 1500 - 1506 (2012/07/28)

Stereoisomers of one of the most important organic compounds, tartaric acid, optically active and meso as well as the ester or amide derivatives, can show diverse structures related to the rotation around the three carbon-carbon bonds. This study determin

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