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6943-65-3

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6943-65-3 Usage

General Description

ETHYLENEBIS(ISOTHIOURONIUM BROMIDE) is a chemical compound commonly used as a biocide and preservative in industrial water treatment systems. It is an effective antimicrobial agent, particularly against bacteria, algae, and fungi, and is often used to control and prevent the growth of these microorganisms in cooling towers, process water, and other industrial systems. The compound works by disrupting the cell membranes of the target microorganisms, leading to their destruction. It is typically applied in liquid form and is known for its stability and long-lasting antimicrobial effects, making it a popular choice for controlling microbial growth in various industrial applications. However, it is important to use this chemical with caution and adhere to safety guidelines to minimize potential health and environmental risks.

Check Digit Verification of cas no

The CAS Registry Mumber 6943-65-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,4 and 3 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 6943-65:
(6*6)+(5*9)+(4*4)+(3*3)+(2*6)+(1*5)=123
123 % 10 = 3
So 6943-65-3 is a valid CAS Registry Number.
InChI:InChI=1/C4H10N4S2/c5-3(6)9-1-2-10-4(7)8/h1-2H2,(H3,5,6)(H3,7,8)

6943-65-3 Well-known Company Product Price

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  • Alfa Aesar

  • (L06784)  Ethylenebis(isothiouronium bromide), 98%   

  • 6943-65-3

  • 5g

  • 163.0CNY

  • Detail
  • Alfa Aesar

  • (L06784)  Ethylenebis(isothiouronium bromide), 98%   

  • 6943-65-3

  • 25g

  • 523.0CNY

  • Detail
  • Alfa Aesar

  • (L06784)  Ethylenebis(isothiouronium bromide), 98%   

  • 6943-65-3

  • 100g

  • 1629.0CNY

  • Detail

6943-65-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-carbamimidoylsulfanylethyl carbamimidothioate,dihydrobromide

1.2 Other means of identification

Product number -
Other names VUF 8332 dihydrobromide

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:6943-65-3 SDS

6943-65-3Relevant articles and documents

The 1,4-dithiin ring opening in 1,4-dithiinodiquinolines as a route to quinoline crown thioethers

Pluta, Krystian

, p. 2861 - 2870 (2007/10/03)

Quinoline crown thioethers (7) and (8) with 8-, 9-, 10-, 11-, 12-, 18-, 20-, 21- and 24-membered macrocyclic thiacrown ring were obtained by the 1,4- dithiin ring opening in 1,4-dithiinodiquinolines (1) and (2) with divalent sulfur nucleophiles followed by S-alkylation with divalent alkylating agents. Thiacrowns (7) and (8) contain two or four quinoline units.

Synthetic ionophores: Part 5 - synthesis of oxa-thia Crown ethers and a study of their ionophore character

Singh,Kumar,Singh,Kumar

, p. 237 - 240 (2007/10/02)

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ORGANIC SYNTHESIS USING PTC-5: NUCLEOPHILIC AROMATIC SUBSTITUTION UNDER LIQUID-LIQUID AND SOLID-LIQUID PHASE TRANSFER CONDITIONS.

Singh, Paramjit,Arora, Geeta

, p. 2625 - 2632 (2007/10/02)

The reaction of 1-chloro-4-nitrobenzene (1) with dithiols generated in situ from thiouronium salts (2) under PT conditions, which in turn have been procured by the reaction of appropriate α,ω-dibromoalkanes with thiourea have been investigated.The reactions of (1) with various diols have also been investigated and their reaction mechanism is discussed.

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