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2620-88-4

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2620-88-4 Usage

General Description

2,2'-dithiobis[N-butylbenzamide], also known as Dibutyldithiocarbamic acid benzyl ester, is a chemical compound commonly used as a rubber accelerator and vulcanization accelerator in the production of tires, belts, and other rubber products. It is also used as an intermediate in the synthesis of pharmaceuticals and agricultural chemicals. 2,2'-dithiobis[N-butylbenzamide] is classified as a dithiocarbamate, and its strong affinity for metal ions makes it a useful chelating agent in metal extraction processes. However, it is important to handle this chemical with caution as it is harmful if swallowed, inhaled, or absorbed through the skin, and it can cause irritation to the eyes, skin, and respiratory system. Personal protective equipment and proper ventilation are recommended when working with this compound.

Check Digit Verification of cas no

The CAS Registry Mumber 2620-88-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,6,2 and 0 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 2620-88:
(6*2)+(5*6)+(4*2)+(3*0)+(2*8)+(1*8)=74
74 % 10 = 4
So 2620-88-4 is a valid CAS Registry Number.

2620-88-4SDS

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 N-butyl-2-[[2-(butylcarbamoyl)phenyl]disulfanyl]benzamide

1.2 Other means of identification

Product number -
Other names Diphenyldisulfid-2,2'-dicarbonsaeure-bis-n-butylamid

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:2620-88-4 SDS

2620-88-4Relevant articles and documents

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

Kang, Jianming,Ferrell, Aaron J.,Chen, Wei,Wang, Difei,Xian, Ming

, p. 852 - 855 (2018)

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

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

Sano, Tomohumi,Takagi, Toshiyuki,Gama, Yasuo,Shibuya, Isao,Shimizu, Masao

, p. 1585 - 1588 (2007/10/03)

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.

Antithrombotic agent

-

, (2008/06/13)

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.

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