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6487-38-3

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6487-38-3 Usage

Description

3-Hydroxypropionic acid is a building block in the synthesis of a variety of compounds with industrial applications, including acrylic acid, acrylamide, and 1,3-propanediol. Accumulation of 3-hydroxypropionic acid is also used as a biomarker of defects in propionic acid and branched-chain amino acid catabolism in patients with methylmalonic acidemia or propionic acidemia.

Chemical Properties

White Solid

Uses

3-Hydroxypropionic Acid Sodium Salt is a beta hydroxy acid derived from plants and crops such as corn. It is used in the preparation of acrylates and biodegradable polymer polyester.

Check Digit Verification of cas no

The CAS Registry Mumber 6487-38-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,4,8 and 7 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6487-38:
(6*6)+(5*4)+(4*8)+(3*7)+(2*3)+(1*8)=123
123 % 10 = 3
So 6487-38-3 is a valid CAS Registry Number.

6487-38-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Hydroxypropionic Acid Sodium Salt

1.2 Other means of identification

Product number -
Other names sodium,3-hydroxypropanoate

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:6487-38-3 SDS

6487-38-3Downstream Products

6487-38-3Relevant articles and documents

PURIFICATION OF 1,3-PROPANEDIOL BY DISTILLATION

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Page 12, (2008/06/13)

The present invention is a process for purification of 1,3-propanediol (PDO) by an inverted distillation sequence which comprises: (a) optionally removing water or other solvents from the crude 1,3-propanediol mixture; (b) distilling the crude 1,3-propanediol mixture under conditions which maximize the separation of components of the mixture which are heavier than 1,3-propanediol from the 1,3-propanediol and the components which are lighter than 1,3-propanediol; (c) drawing off a stream which contains at least most of the 1,3-propanediol and at least some of the components of the mixture which are lighter than 1,3-propanediol; and (d) distilling the stream of (c) to separate the 1,3-propanediol from components in the stream which are lighter than 1,3-propanediol and any residual components which are heavier than 1,3-propanediol.

AMIDRAZONES 9. CONVENIENT SYNTHESIS OF 1-ALKYL-1-PHENYLHYDRAZINES AND α,β-UNSATURATED AMIDRAZONES VIA BASE-PROMOTED REACTIONS OF 1,1-DISUBSTITUTED-3-AMNIO-4,5-DIHYDRO-1H-PYRAZOLIUM SALTS.

Smith, Richard F.,Olson, Laurie A.,Ryan, William J.,Coffman, Karen J.,Galante, Julienne M.,et al.

, p. 585 - 596 (2007/10/02)

A simple, efficient procedure for the conversion of phenylhydrazine to 1-alkyl-1-phenylhydrazines via base-promoted hydrolysis of 1-alkyl-3-amino-4,5-dihydro-1-phenyl-1H-pyrazolium iodides (2) is described.N',N'-disubstituted hydrazones of trans-cinnamamide and acrylamide are obtained by Hofmann-type ring openings of 1,1-disubstituted-3-amino-4,5-dihydro-5-phenyl (or 5-unsubstituted) -1H-pyrazolium halides (5,7).

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