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CAS

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38499-08-0

Triphenylmethanesulfenamide is a chemical compound that serves as an accelerator in the production of rubber and other polymers, enhancing the curing process and improving the material's tensile strength, elasticity, and thermal stability. It is also utilized as a stabilizer in various products such as cosmetics, adhesives, and sealants. However, it requires careful handling due to its potential to cause skin irritation and allergic reactions in some individuals.

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  • 38499-08-0 Structure

  • Basic information

    1. Product Name: TRIPHENYLMETHANESULFENAMIDE
    2. Synonyms: TRIPHENYLMETHANESULFENAMIDE;Triphenylmethanesulfonamide.;TRIPHENYLMETHANESULPHENAMIDE;S-tritylthiohydroxylamine
    3. CAS NO:38499-08-0
    4. Molecular Formula: C19H17NS
    5. Molecular Weight: 291.41
    6. EINECS: N/A
    7. Product Categories: Organic Building Blocks;Others;Sulfur Compounds
    8. Mol File: 38499-08-0.mol

  • Chemical Properties

    1. Melting Point: 128-130 °C(lit.)
    2. Boiling Point: 437.9 °C at 760 mmHg
    3. Flash Point: 218.6 °C
    4. Appearance: /
    5. Density: 1.163 g/cm3
    6. Vapor Pressure: 7.19E-08mmHg at 25°C
    7. Refractive Index: 1.647
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: TRIPHENYLMETHANESULFENAMIDE(CAS DataBase Reference)
    11. NIST Chemistry Reference: TRIPHENYLMETHANESULFENAMIDE(38499-08-0)
    12. EPA Substance Registry System: TRIPHENYLMETHANESULFENAMIDE(38499-08-0)

  • Safety Data

    1. Hazard Codes: Xi
    2. Statements: 36/37/38
    3. Safety Statements: 26-37/39
    4. WGK Germany: 3
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 38499-08-0(Hazardous Substances Data)

38499-08-0 Usage

Uses

Used in Rubber and Polymer Production:
Triphenylmethanesulfenamide is used as an accelerator for speeding up the curing process of rubber and other polymers, which results in improved tensile strength, elasticity, and thermal stability of the final product.
Used in Cosmetics:
In the cosmetics industry, triphenylmethanesulfenamide is used as a stabilizer to maintain the quality and consistency of cosmetic products, ensuring their longevity and effectiveness.
Used in Adhesives and Sealants:
Triphenylmethanesulfenamide is employed as a stabilizer in adhesives and sealants to enhance their performance and durability, providing better bonding and sealing properties.

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.

Studies on the Preparation and Reactions of Tritylsulfenimines

Branchaud, Bruce P.

, p. 3531 - 3538 (2007/10/02)

Carbonyl compounds react with stable, crystalline triphenylmethanesulfenamide (TrSNH2, 4) under mild conditions to form tritylsulfenimines 5 and 6.Lithiation of acetone tritylsulfenimine (5c) at O deg C led to a novel rearrangement-decomposition producing

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