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3-Pyrrolidinone, also known as 1-Methyl-2-pyrrolidinone, is a colorless liquid with a slightly ammonia-like odor. It is a five-membered lactam that is commonly used as a versatile solvent in various applications due to its ability to dissolve a wide range of materials. Its high boiling point and low vapor pressure contribute to its stability and reliability in industrial processes.

96-42-4

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96-42-4 Usage

Uses

Used in Pharmaceutical Industry:
3-Pyrrolidinone is used as a solvent for the production of pharmaceuticals, facilitating the dissolution and processing of various compounds in the manufacturing of drugs.
Used in Agrochemical Industry:
3-Pyrrolidinone is used as a solvent in the production of agrochemicals, aiding in the formulation and application of pesticides and other agricultural chemicals.
Used in Polymer Industry:
3-Pyrrolidinone is used as a solvent in the synthesis and processing of polymers, contributing to the development of new materials with specific properties.
Used in Electronics Industry:
3-Pyrrolidinone is used as a solvent in the electronics industry, particularly for the cleaning and processing of electronic components, due to its ability to dissolve a wide range of materials.
It is important to handle 3-Pyrrolidinone with caution, as it can cause skin and eye irritation. It should be used in well-ventilated areas to ensure safety during its application in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 96-42-4 includes 5 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 2 digits, 9 and 6 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 96-42:
(4*9)+(3*6)+(2*4)+(1*2)=64
64 % 10 = 4
So 96-42-4 is a valid CAS Registry Number.
InChI:InChI=1/C4H7NO/c6-4-1-2-5-3-4/h5H,1-3H2

96-42-4SDS

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 pyrrolidin-3-one

1.2 Other means of identification

Product number -
Other names 3-Oxo-pyrrolidin

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:96-42-4 SDS

96-42-4Relevant academic research and scientific papers

Synthesis and in-vitro activity of new 1β-methylcarbapenem derivatives as antibacterial agents

Jung, Myung-Ho,Joon, Hee Hong,Cho, Jung-Hyuck,Oh, Chang-Hyun

scheme or table, p. 780 - 786 (2009/04/07)

The synthesis of a new series of 1β-methylcarbapenems having pyrrolidine and piperidine moieties is described. Their in-vitro antibacterial activities against both Gram-positive and Gram-negative bacteria were tested and the effect of substituents on the pyrrolidine ring was investigated. A particular compound III b having an oxime-pyrrolidine moiety showed the most potent antibacterial activity.

Identification of a novel class of succinyl-nitrile-based Cathepsin S inhibitors

Bekkali, Younes,Thomson, David S.,Betageri, Raj,Emmanuel, Michel J.,Hao, Ming-Hong,Hickey, Eugene,Liu, Weimin,Patel, Usha,Ward, Yancey D.,Young, Erick R.R.,Nelson, Richard,Kukulka, Alison,Brown, Maryanne L.,Crane, Kathy,White, Della,Freeman, Dorothy M.,Labadia, Mark E.,Wildeson, Jessi,Spero, Denice M.

, p. 2465 - 2469 (2008/03/11)

The synthesis and in vitro activities of a series of succinyl-nitrile-based inhibitors of Cathepsin S are described. Several members of this class show nanomolar inhibition of the target enzyme as well as cellular potency. The inhibitors displaying the greatest potency contain N-alkyl substituted piperidine and pyrrolidine rings spiro-fused to the α-carbon of the P1 residue.

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