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96927-56-9

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96927-56-9 Usage

General Description

DL-GLUTAMIC-2,4,4-D3 ACID is a isotopically labeled form of L-glutamic acid, an important non-essential amino acid that plays a crucial role in protein synthesis and the functioning of the nervous system. It is also a key component of the citric acid cycle, which is involved in the production of energy within cells. DL-GLUTAMIC-2,4,4-D3 ACID is commonly used as a research tool for studying the metabolism and functions of glutamic acid in biological systems.

Check Digit Verification of cas no

The CAS Registry Mumber 96927-56-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,9,2 and 7 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 96927-56:
(7*9)+(6*6)+(5*9)+(4*2)+(3*7)+(2*5)+(1*6)=189
189 % 10 = 9
So 96927-56-9 is a valid CAS Registry Number.

96927-56-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name DL-GLUTAMIC-2,4,4-D3 ACID

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:96927-56-9 SDS

96927-56-9Upstream product

96927-56-9Downstream Products

96927-56-9Relevant articles and documents

Convenient Synthesis of Stereospecifically Deuteriated Glycines from Glutamic Acid using a Combination of Enzymatic and Chemical Methods

Santaniello, Enzo,Casati, Rosangela,Manzocchi, Ada

, p. 2389 - 2392 (2007/10/02)

Chiral glycines (1a) and (1b) have been synthesized starting from stereospecifically deuteriated 4-aminobutanoic acids (3a) and (3b).Enzymatic decarboxylation of (2S)-glutamic acid (2a) in (2)H2O and (2R,S)-glutamic acid (2b) + (2c) in H2O afforded (3a) and (3b), respectively.Chemical transformations of deuteriated pyrrolidinones (4a) and (4b) afforded stereospecifically labelled glycines (1a) and (1b) in good yields.

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