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80-60-4

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80-60-4 Usage

General Description

DL-2-aminobutyric acid is a chemical compound with the molecular formula C4H9NO2. It is an amino acid derivative that is structurally similar to gamma-aminobutyric acid (GABA), a neurotransmitter involved in the central nervous system. DL-2-aminobutyric acid is used in research and pharmaceutical applications to study the effects of GABA and related compounds on neurological function and to develop potential treatments for conditions such as anxiety, epilepsy, and neuropathic pain. It is also being investigated for its potential role in modulating neurotransmitter activity in the brain. Additionally, DL-2-aminobutyric acid has some potential as a biomarker for certain metabolic disorders and it may have applications in the production of pharmaceuticals.

Check Digit Verification of cas no

The CAS Registry Mumber 80-60-4 includes 5 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 2 digits, 8 and 0 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 80-60:
(4*8)+(3*0)+(2*6)+(1*0)=44
44 % 10 = 4
So 80-60-4 is a valid CAS Registry Number.
InChI:InChI=1S/C4H9NO2/c1-2-3(5)4(6)7/h3H,2,5H2,1H3,(H,6,7)

80-60-4SDS

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 DL-2-AMINOBUTYRIC ACID

1.2 Other means of identification

Product number -
Other names a-Aminobutyric Acid

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:80-60-4 SDS

80-60-4Downstream Products

80-60-4Relevant articles and documents

METHOD OF SEPARATING AND COLLECTING OPTICALLY ACTIVE AMINO ACID AMIDE

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Page/Page column 11-12;13, (2008/06/13)

[PROBLEMS] To provide a method of efficiently separating and collecting an optically active amino acid amide and an optically active amino acid, which are highly important substances as intermediates in producing various industrial products, pesticides and medicines, from an aqueous solution containing the optically active amino acid amide and the optically active amino acid. [MEANS FOR SOLVING PROBLEMS] In separating and collecting an optically active amino acid amide from an aqueous solution containing the optically active amino acid amide and an optically active amino acid by using the difference in solubility in an organic solvent between the optically active amino acid amide and the optically active amino acid, the separation/collection procedures are carried out, without desalting the aqueous solution or after desalting the same, under such conditions that the ratio (C/A) of the sum of the anionic equivalents (A) contained in the aqueous solution to the sum of the cation equivalents (C) ranges from 0.95 to 1.05 in the case of the non-desalted aqueous solution, or from 0.5 to 1.5 in the case of the desalted aqueous solution.

Resolution of Underivatized Amino Acids by Reversed-Phase Chromatography

Gil-Av, E.,Tishbee, A.,Hare, P. E.

, p. 5115 - 5117 (2007/10/02)

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