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38499-08-0

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38499-08-0 Usage

General Description

Triphenylmethanesulfenamide is a chemical compound commonly used as an accelerator in the production of rubber and other polymers. Its main function is to speed up the curing process of these materials. When added to rubber, it helps to improve its tensile strength, elasticity, and thermal stability. Triphenylmethanesulfenamide is also used as a stabilizer in various products, including cosmetics, adhesives, and sealants. However, it is important to handle this chemical with caution, as it can irritate the skin and cause allergic reactions in some individuals.

Check Digit Verification of cas no

The CAS Registry Mumber 38499-08-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,4,9 and 9 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 38499-08:
(7*3)+(6*8)+(5*4)+(4*9)+(3*9)+(2*0)+(1*8)=160
160 % 10 = 0
So 38499-08-0 is a valid CAS Registry Number.
InChI:InChI=1/C19H17NS/c20-21-19(16-10-4-1-5-11-16,17-12-6-2-7-13-17)18-14-8-3-9-15-18/h1-15H,20H2

38499-08-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name S-tritylthiohydroxylamine

1.2 Other means of identification

Product number -
Other names Triphenylmethanesulfenamide

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:38499-08-0 SDS

38499-08-0Relevant articles and documents

The Synthesis of Substituted thio>acetic Acids

Woulfe, Steven R.,Miller, Marvin J.

, p. 3133 - 3139 (2007/10/02)

The synthesis of substituted thio>acetic acids (6, thiamazins) is described.Various substituted 3(S)-(acylamino)-2-azetidinones were sulfenylated with tert-butyl (phtalimidothio)acetate.Deprotection of the tert-butyl ester with trifluoroacetic acid provided the title compounds.In sharp contrast to their oxygen analogues (oxamazins), the thiamazins were devoid of biological activity.

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