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Butanethioic acid, also known as butane-1-thiol or butyl mercaptan, is a colorless, flammable, and highly volatile liquid with a strong, offensive odor. It is an organic compound belonging to the class of thiols, characterized by the presence of a sulfur-hydrogen bond (-SH). The chemical formula for butanethioic acid is C4H10S, and it has a molecular weight of 90.187 g/mol. Butanethioic acid is primarily used as a chemical intermediate in the production of various chemicals, such as rubber accelerators, pesticides, and pharmaceuticals. Additionally, it is employed as a flavoring agent in the food industry to impart a cooked or roasted flavor to certain products. Due to its pungent smell, butanethioic acid is also used as an odorant in natural gas to detect leaks, as it is added to odorless natural gas to make it easily detectable by humans.

3931-64-4

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3931-64-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3931-64-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,9,3 and 1 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 3931-64:
(6*3)+(5*9)+(4*3)+(3*1)+(2*6)+(1*4)=94
94 % 10 = 4
So 3931-64-4 is a valid CAS Registry Number.

3931-64-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name thiolobutyric acid

1.2 Other means of identification

Product number -
Other names butanethioic S-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:3931-64-4 SDS

3931-64-4Relevant academic research and scientific papers

Product selectivity in the electroreduction of thioesters

We?wer,Olivero,Du?ach

, p. 1709 - 1714 (2007/10/03)

The electroreduction of differently substituted aromatic and aliphatic thioesters (RCOSR′) led to regioselective reactions depending on the nature of the substituents. Thus, the cleavage between the carbonyl group and the SR′ group afforded α-diketones an

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