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Thiopropionic acid S-isopropyl ester, also known as S-isopropyl propylxanthate or S-isopropyl ethyl xanthogenate, is an organic compound with the chemical formula C6H12OS2. It is a colorless liquid that is soluble in organic solvents and has a pungent odor. Thiopropionic acid S-isopropyl ester is primarily used as a vulcanization accelerator in the rubber industry, enhancing the elasticity and strength of rubber products. It is also employed as a flotation agent in the mining industry, where it helps in the separation of valuable minerals from waste materials. Thiopropionic acid S-isopropyl ester is synthesized by reacting isopropanol with thiopropionic acid, and its chemical properties include reactivity with metals and bases. Due to its potential health and environmental risks, it is important to handle this chemical with proper safety measures.

2432-47-5

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2432-47-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2432-47-5 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, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 2432-47:
(6*2)+(5*4)+(4*3)+(3*2)+(2*4)+(1*7)=65
65 % 10 = 5
So 2432-47-5 is a valid CAS Registry Number.

2432-47-5SDS

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-isopropyl thiol-propionate

1.2 Other means of identification

Product number -
Other names Isopropyl-thiopropionat

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:2432-47-5 SDS

2432-47-5Relevant academic research and scientific papers

The Reductive Acylation of Organic Disulfides with Aldehydes under Photochemical and Radical Conditions

Takagi, Makoto,Goto, Setsuo,Tazaki, Masato,Matsuda, Tsutomu

, p. 1982 - 1987 (1980)

The irradiation of organic disulfides in aldehyde solvents resulted in the reductive fission of the S-S linkage, giving an equimolar mixture of the corresponding thiol and thiol acylate in a good yield.The cyclic disulfides gave mono S-acylated dithiols.The reaction proceeded by means of the photo-initiated radical chain mechanism, and AIBN (azobisisobutyronitrile) effected the same reaction under thermal conditions.

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