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N-(3,4-Dichlorophenyl)guanidine, with the molecular formula C7H6Cl2N2, is a white crystalline solid that serves as an effective antimicrobial agent and preservative. Its chemical structure endows it with the ability to inhibit the growth of bacteria and fungi, making it a valuable component in various applications across different industries.

65783-10-0

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65783-10-0 Usage

Uses

Used in Personal Care Products:
N-(3,4-Dichlorophenyl)guanidine is used as a preservative in personal care products such as shampoos, soaps, and deodorants for its ability to prevent spoilage by inhibiting the growth of bacteria and fungi.
Used in Rubber and Plastics Manufacturing:
In the manufacturing industry, N-(3,4-Dichlorophenyl)guanidine is utilized in the production of rubber and plastics, contributing to the enhancement of their properties and performance.
Used in Industrial Water Treatment:
N-(3,4-Dichlorophenyl)guanidine is also employed in the treatment of industrial water systems, where it helps control microbial growth to maintain the efficiency and safety of these systems.
It is crucial to handle N-(3,4-Dichlorophenyl)guanidine with care due to its potential toxicity if ingested or inhaled, and its capacity to cause skin and eye irritation. Adhering to proper safety measures is essential when working with this chemical to minimize the risk of exposure.

Check Digit Verification of cas no

The CAS Registry Mumber 65783-10-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,7,8 and 3 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 65783-10:
(7*6)+(6*5)+(5*7)+(4*8)+(3*3)+(2*1)+(1*0)=150
150 % 10 = 0
So 65783-10-0 is a valid CAS Registry Number.

65783-10-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(3,4-dichlorophenyl)guanidine

1.2 Other means of identification

Product number -
Other names N-(3,4-dichlorophenyl)guanidine nitrate

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:65783-10-0 SDS

65783-10-0Relevant academic research and scientific papers

Facile synthesis of 2,4-diamino-6-alkyl- or 6-aryl-pyrimidine derivatives

Wang, Xihong,Sathunuru, Ramadas,Melendez, Victor,Kozar, Michael P.,Lin, Ai J.

scheme or table, p. 1056 - 1061 (2010/10/21)

(Chemical Equation Presented) Facile methods were developed to prepare a series of 6-phenyl and 6-alkyl-2,4-diaminopyrimidine derivatives. The pyrimidine ring of the final products was constructed by treatment of a 1,3-dicarbonyl derivative with an amidin

2-Guanidinylimidazolidinedione compounds and methods of making and using thereof

-

Page/Page column 7-8; 10; 12-13, (2010/02/12)

Disclosed herein are 2-guanidinylimidazolidinedione compounds having the structural formula A or B wherein R1 and R2 are each independently a hydrogen, halogen, alkyl, alkoxyl, amino, alkylamino or aralkyl, and wherein R3

Unambiguous synthesis and prophylactic antimalarial activities of imidazolidinedione derivatives

Zhang, Quan,Guan, Jian,Sacci, John,Ager, Arba,Ellis, William,Milhous, Wilbur,Kyle, Dennis,Lin, Ai J.

, p. 6472 - 6481 (2007/10/03)

WR182393, a guanidinoimidazolidinedione derivatives with potent causal prophylactic antimalarial activity by intramuscular injection, was previouly prepared by treatment of chloroproguanil and diethyl oxalate, yielding a mixture of two closely related iso

PYRADAZINE COMPOUNDS AS GSK-3 INHIBITORS

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Page 94-95, (2008/06/13)

The present invention relates generally to inhibitors of the kinases, such as GSK3, and more particularly to fused pyradazine compounds according to formula (I) and methods of their use.

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