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70607-84-0

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70607-84-0 Usage

Uses

2-Pyrrolidinone-3,3,4,4,5,5-d6 is D6 labelled 2-Pyrrolidinone which is widely used organic polar solvent for various applications. 2-Pyrrolidinone is also an intermediate in the manufacture of polymers.

Check Digit Verification of cas no

The CAS Registry Mumber 70607-84-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,6,0 and 7 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 70607-84:
(7*7)+(6*0)+(5*6)+(4*0)+(3*7)+(2*8)+(1*4)=120
120 % 10 = 0
So 70607-84-0 is a valid CAS Registry Number.

70607-84-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-PYRROLIDINONE-3,3,4,4,5,5-D6

1.2 Other means of identification

Product number -
Other names 2-pyrrolidin-3-yl-pyridine

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:70607-84-0 SDS

70607-84-0Upstream product

70607-84-0Downstream Products

70607-84-0Relevant articles and documents

Detection of the in vivo conversion of 2-pyrrolidinone to γ-aminobutyric acid in mouse brain

Callery,Stogniew,Geelhaar

, p. 23 - 26 (1979)

Labeled γ-aminobutyric acid was detected in mouse brain following intravenous injections of deuterium labeled 2-pyrrolidinone. [2H6]Pyrrolidinone was prepared by the reduction of [2H4]succinimide with lithium aluminum deuteride. Quantification was accomplished by a gas chromatography mass spectrometry assay method. γ-Aminobutyric acid and internal standard, 5-aminovaleric acid, were converted to volatile derivatives by treatment with N,N-dimethylformamide dimethyl acetal. Quantitative estimates were derived from peak area measurements obtained from monitoring the parent ions of the γ-aminobutyric acid and internal standard derivatives by repetitive scanning during the GC run. The conversion of pyrrolidinone to γ-aminobutyric acid may provide a method for labelling central γ-aminobutyric acid pools.

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