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Butyl hydrogen carbonotrithioate, also known as butyl xanthogen carbonate, is an organic compound with the chemical formula C5H10OSS. It is a colorless to pale yellow liquid that is soluble in organic solvents and has a pungent odor. butyl hydrogen carbonotrithioate is primarily used as a vulcanization accelerator in the rubber industry, enhancing the speed and quality of rubber's reaction with sulfur. It is also employed as a flame retardant and a stabilizer in various chemical processes. Due to its reactivity, butyl hydrogen carbonotrithioate requires careful handling and is typically stored in a cool, dry place away from heat and direct sunlight.

928-48-3

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928-48-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 928-48-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,2 and 8 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 928-48:
(5*9)+(4*2)+(3*8)+(2*4)+(1*8)=93
93 % 10 = 3
So 928-48-3 is a valid CAS Registry Number.

928-48-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name potassium,butylsulfanylmethanedithioic acid

1.2 Other means of identification

Product number -
Other names potassium 4-pyridinyldithiocarbazate

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:928-48-3 SDS

928-48-3Relevant academic research and scientific papers

2,2,4,4-Tetrathio substituted 1,3-dithietanes

Weber, Wolfgang,Chirowodza, Helen,Pasch, Harald

, p. 2017 - 2021 (2013/03/14)

The synthesis of 2,2,4,4-tetrathio substituted 1,3-dithietanes and their intermediates by reaction of thiophosgene with carbonotrithioates or O-ethyldithiocarbonate is reported. Their reactivity against thermolysis and aminolysis was investigated.

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