2620-88-4

Usage

Uses

Used in Rubber Industry:
2,2'-dithiobis[N-butylbenzamide] is used as a rubber accelerator and vulcanization accelerator for the production of tires, belts, and other rubber products. It enhances the curing process, improving the rubber's strength, elasticity, and durability.
Used in Pharmaceutical and Agricultural Chemical Industries:
2,2'-dithiobis[N-butylbenzamide] serves as an intermediate in the synthesis of various pharmaceuticals and agricultural chemicals. Its unique chemical properties allow for the development of new compounds with specific therapeutic or pesticidal effects.
Used in Metal Extraction Processes:
As a chelating agent, 2,2'-dithiobis[N-butylbenzamide] is utilized in metal extraction processes. Its strong affinity for metal ions enables efficient separation and recovery of valuable metals from various sources.
Safety Precautions:
When working with 2,2'-dithiobis[N-butylbenzamide], it is crucial to use personal protective equipment, such as gloves, goggles, and respirators, to minimize the risk of exposure. Additionally, proper ventilation should be maintained in the workspace to reduce the concentration of airborne particles and vapors.

Upstream product

• 1677-27-6 3H-1,2-benzodithiol-3-one 
• 109-73-9 N-butylamine 
• 119-80-2 2,2'-dithiobenzoic acid 
• 147-93-3 Thiosalicylic acid 
• 19602-82-5 2,2'-dithiodibenzoic acid dichloride 
• 38058-01-4 2,2-dimethyl-4H-benzo[d][1,3]oxathiin-4-one 

Downstream Products

• 4299-07-4 2-butyl-1,2-benzothiazolin-3-one 
• 58249-32-4 2-mercapto-benzoic acid butylamide 

Relevant academic research and scientific papers

Cyclic Acyl Disulfides and Acyl Selenylsulfides as the Precursors for Persulfides (RSSH), Selenylsulfides (RSeSH), and Hydrogen Sulfide (H2S)

The reactions of three model compounds (1-3) for cyclic acyl disulfides and cyclic acyl selenylsulfides are studied. These compounds were found to be effective precursors for persulfides (RSSH) and selenylsulfides (RSeSH) upon reacting with nucleophilic s

Crucial role of selenium in the virucidal activity of benzisoselenazol- 3(2h)-ones and related diselenides

Various N-substituted benzisoselenazol-3(2H)-ones and their non-seleniumcontaining analogues have been synthesized and tested against selected viruses (HHV-1, EMCV and VSV) to determine the extent to which selenium plays a role in antiviral activity. The data presented here show that the presence of selenium is crucial for the antiviral properties of benzisoselenazol-3(2H)-ones since their isostructural analogues having different groups but lacking selenium either did not show any antiviral activity or their activity was substantially lower. The open-chain analogues of benzisoselenazol- 3(2H)-ones-diselenides also exhibited high antiviral activity while selenides and disulfides were completely inactive towards model viruses.

A practical synthesis of N-substituted 1,2-benzisothiazolin-3-ones from N,N′-disubstituted 2,2′-dithiodibenzamides

A variety of N-substituted 1,2-benzisothiazolin-3-ones were easily synthesized from N,N′-disubstituted 2,2′-dithiodibenzamides in the presence of O-methylhydroxylamine hydrochloride. Derivatives with a primary, secondary, or tertiary alkyl group or an aryl group on the N-1 nitrogen of the 1,2-benzisothiazolin-3-one were obtained.

Preparation and properties of 3,1-benzoxathian-4-one derivatives

A simple preparation of 3,1-benzoxathian-4-one derivatives (3) from thiosalicylic acid and aldehydes, methyl and cyclic ketones, as well as 2,2-dimethoxypropane was developed. The reactivity of 3 under nucleophilic, acidic, reductive and oxidative conditions was examined.

Antithrombotic agent

Certain 2,2'-dithiobis-N-substituted or unsubstituted benzamides or derivatives thereof are useful as antithrombotic agents because of their ability to suppress aggregation of blood platelets.