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Hexanethioic acid S-butyl ester, also known as butyl hexyl sulfide, is an organic compound with the chemical formula C10H20S. It is a colorless liquid with a strong, unpleasant odor and is derived from the esterification of hexanethioic acid and butanol. Hexanethioic acid S-butyl ester is primarily used as a synthetic flavoring agent in the food and beverage industry, as well as a fragrance component in the production of perfumes and cosmetics. It is also employed as a solvent and a chemical intermediate in various industrial applications. Due to its potential health risks, it is essential to handle hexanethioic acid S-butyl ester with caution and in accordance with safety guidelines.

2432-79-3

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2432-79-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2432-79-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,4,3 and 2 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 2432-79:
(6*2)+(5*4)+(4*3)+(3*2)+(2*7)+(1*9)=73
73 % 10 = 3
So 2432-79-3 is a valid CAS Registry Number.
InChI:InChI=1/C10H20OS/c1-4-6-7-8-10(11)12-9(3)5-2/h9H,4-8H2,1-3H3

2432-79-3SDS

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 S-butan-2-yl hexanethioate

1.2 Other means of identification

Product number -
Other names S-butyl hexanethioate

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:2432-79-3 SDS

2432-79-3Downstream Products

2432-79-3Relevant academic research and scientific papers

Synthesis of S-Alkyl Alkanethioates via 1-Iodoalk-1-enyldialkylboranes

Hoshi, Masayuki,Masuda, Yuzuru,Arase, Akira

, p. 714 - 715 (1985)

S-Alkyl alkanethioates were formed in high yields by successive reactions of 1-iodoalk-1-enyl-bis(1,2-dimethylpropyl)boranes with alkylthiomagnesium bromides and alkaline hydrogen peroxide.

The hydroboration of 1-alkylthio-1-alkynes, and its application to the syntheses of s-alkyl alkanethioates and (Z)-1-alkylthio-1-alkenes

Hoshi,Masuda,Arase

, p. 447 - 452 (2007/10/02)

Hydroboration of 1-alkylthio-1-alkynes with dicyclohexylborane or bis(1,2-dimethylpropyl)borane proceeded smoothly, adding most of the dialkylboryl group to the α-position of the triple bond. The resulting alkenylboranes afforded either S-alkyl alkanethio

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