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72377-05-0

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72377-05-0 Usage

General Description

(S)-2-Ethylhexanoic acid, also known as (S)-2-Ethylhexanoate, is a carboxylic acid with the chemical formula C8H16O2. It is a colorless liquid with a fruity odor, and is used as a chemical intermediate in the production of various substances such as pharmaceuticals, plasticizers, and fragrances. It is also commonly used as a precursor for the synthesis of metal soaps, which are used as paint driers and lubricants. (S)-2-Ethylhexanoic acid is considered to be relatively non-toxic and is not classified as a hazardous substance, making it a widely used and versatile chemical compound in various industrial applications.

Check Digit Verification of cas no

The CAS Registry Mumber 72377-05-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,3,7 and 7 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 72377-05:
(7*7)+(6*2)+(5*3)+(4*7)+(3*7)+(2*0)+(1*5)=130
130 % 10 = 0
So 72377-05-0 is a valid CAS Registry Number.

72377-05-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S)-ethylhexanoic acid

1.2 Other means of identification

Product number -
Other names S-(+)-2-ethylhexanoic 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:72377-05-0 SDS

72377-05-0Upstream product

72377-05-0Relevant articles and documents

Directed evolution of an enantioselective lipase with broad substrate scope for hydrolysis of α-substituted esters

Engstroem, Karin,Nyhlen, Jonas,Sandstroem, Anders G.,Baeckvall, Jan-E.

supporting information; experimental part, p. 7038 - 7042 (2010/07/05)

A variant of Candida antarctica lipase A (CalA) was developed for the hydrolysis of α-substituted p-nitrophenyl esters by directed evolution. The E values of this variant for 7 different esters was 45-276, which is a large improvement compared to 2-20 for the wild type. The broad substrate scope of this enzyme variant is of synthetic use, and hydrolysis of the tested substrates proceeded with an enantiomeric excess between 95-99%. A 30-fold increase in activity was also observed for most substrates. The developed enzyme variant shows (R)-selectivity, which is reversed compared to the wild type that is (S)-selective for most substrates.

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