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63709-57-9

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63709-57-9 Usage

Description

2,3-dichloro-6-(2,4-dichlorophenoxy)phenol is a chlorinated derivative of the antimicrobial agent triclosan, which is widely recognized for its effectiveness in inhibiting the growth of various microorganisms. 2,3-dichloro-6-(2,4-dichlorophenoxy)phenol is characterized by its chemical structure that features two chlorine atoms at the 2nd and 3rd positions, and a 2,4-dichlorophenoxy group attached to the 6th position of the phenol molecule. Its unique structure endows it with potent antimicrobial properties, making it a valuable compound for various applications.

Uses

Used in Environmental Testing and Research:
2,3-dichloro-6-(2,4-dichlorophenoxy)phenol is utilized as a standard for environmental testing and research, particularly in the assessment of the presence and impact of chlorinated compounds in various ecosystems. Its role in this context is crucial for understanding the potential ecological risks associated with the use of chlorinated antimicrobial agents and for developing strategies to mitigate their adverse effects on the environment.
Used in Antimicrobial Applications:
As a derivative of triclosan, 2,3-dichloro-6-(2,4-dichlorophenoxy)phenol is employed in various antimicrobial applications, including the development of personal care products, medical devices, and industrial materials. Its ability to inhibit the growth of bacteria, fungi, and other microorganisms makes it a valuable component in the formulation of products designed to maintain hygiene and prevent the spread of infections.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2,3-dichloro-6-(2,4-dichlorophenoxy)phenol is used as an active ingredient in the development of antimicrobial drugs and treatments. Its potent antimicrobial properties make it a promising candidate for the treatment of various bacterial and fungal infections, particularly those that are resistant to conventional antibiotics and antifungal agents.
Used in Agriculture:
2,3-dichloro-6-(2,4-dichlorophenoxy)phenol is also utilized in the agricultural sector as a component of pesticides and fungicides. Its antimicrobial properties help protect crops from diseases caused by pathogenic microorganisms, thereby contributing to increased crop yields and improved food security.

Check Digit Verification of cas no

The CAS Registry Mumber 63709-57-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,7,0 and 9 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 63709-57:
(7*6)+(6*3)+(5*7)+(4*0)+(3*9)+(2*5)+(1*7)=139
139 % 10 = 9
So 63709-57-9 is a valid CAS Registry Number.
InChI:InChI=1/C12H6Cl4O2/c13-6-1-3-9(8(15)5-6)18-10-4-2-7(14)11(16)12(10)17/h1-5,17H

63709-57-9SDS

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 2,3-Dichloro-6-(2,4-dichlorophenoxy)phenol

1.2 Other means of identification

Product number -
Other names 2',3,4,4'-Tetrachloro-2-hydroxydiphenyl ether

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:63709-57-9 SDS

63709-57-9Upstream product

63709-57-9Downstream Products

63709-57-9Relevant articles and documents

Real-time detection and identification of aqueous chlorine transformation products using QTOF MS

Vanderford, Brett J.,Mawhinney, Douglas B.,Rosario-Ortiz, Fernando L.,Snyder, Shane A.

, p. 4193 - 4199 (2008)

A screening technique has been developed that allows the rapid, real-time detection and identification of major transformation products of organic contaminants during aqueous oxidation experiments. In this technique, a target contaminant is dissolved in b

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