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72676-55-2

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72676-55-2 Usage

Description

5,5'-dithiodi-1,3,4-thiadiazole-2(3H)-thione is a chemical compound known for its unique properties and versatile applications across various industries. It is characterized by its ability to act as a vulcanizing agent, crosslinking agent, and additive for metallic surfaces, making it a valuable component in the manufacturing and processing of certain materials.

Uses

Used in Rubber Industry:
5,5'-dithiodi-1,3,4-thiadiazole-2(3H)-thione is used as a rubber vulcanizing agent for chlorinated polyethylene (CPE) rubber. It enhances the rubber's properties, such as strength, elasticity, and durability, by facilitating the crosslinking process between polymer chains.
Used in Rubber Crosslinking:
As a rubber crosslinking agent, 5,5'-dithiodi-1,3,4-thiadiazole-2(3H)-thione plays a crucial role in improving the overall performance of rubber products. It helps in creating a network of chemical bonds between polymer chains, resulting in increased stability and resistance to deformation.
Used in Metallic Surface Treatment:
5,5'-dithiodi-1,3,4-thiadiazole-2(3H)-thione is also utilized as an additive for metallic surfaces. It contributes to the enhancement of surface properties, such as corrosion resistance, wear resistance, and adhesion, making it suitable for various applications in the metalworking and manufacturing industries.
Used in Cured Chlorinated Polyethylene (CPE):
In the production of cured CPE, 5,5'-dithiodi-1,3,4-thiadiazole-2(3H)-thione is employed to improve the material's performance characteristics. It aids in the vulcanization process, leading to a more robust and reliable end product with enhanced mechanical properties and resistance to environmental factors.

Flammability and Explosibility

Nonflammable

Check Digit Verification of cas no

The CAS Registry Mumber 72676-55-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,6,7 and 6 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 72676-55:
(7*7)+(6*2)+(5*6)+(4*7)+(3*6)+(2*5)+(1*5)=152
152 % 10 = 2
So 72676-55-2 is a valid CAS Registry Number.

72676-55-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-[(2-sulfanylidene-3H-1,3,4-thiadiazol-5-yl)disulfanyl]-3H-1,3,4-thiadiazole-2-thione

1.2 Other means of identification

Product number -
Other names 3H,3'H-5,5'-disulfanediyl-bis-[1,3,4]thiadiazole-2-thione

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Lubricants and lubricant additives,Process regulators
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:72676-55-2 SDS

72676-55-2Downstream Products

72676-55-2Relevant articles and documents

THE PHOTOLYSIS OF 1,3,4-THIADIAZOLIDINE-2,5-DITHIONES IN PRESENCE AND IN ABSENCE OF SINGLET OXYGEN

Zayed, M. F.,Hafez, T. S.,El-Din, N. Khir,Hefny, E.

, p. 51 - 55 (2007/10/02)

The photolysis of 1,3,4-thiadiazolidine-2,5-dithiones (Ia-c) in methanol has been studied.The disulphides IIa-c were isolated and identified.Dye sensitized photooxygenation of compounds Ia-c were also studied.Compounds IIa, IIIa and IVa were produced in case of Ia, and IIb and IIIb were produced in Ib, and IIc and IIIc were produced in Ic.A mechanism for the formation of these compounds is presented.

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