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74098-29-6

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74098-29-6 Usage

Description

6-CHLORO-3,4-DIMETHYL-2-NITROPHENOL, also known as PCMX, is a chemical compound that serves as an effective antiseptic and disinfectant. It is characterized by its yellow, crystalline solid form and a slightly phenolic odor. PCMX is soluble in alcohol, ether, and chloroform, and it demonstrates potent antimicrobial properties against an extensive spectrum of bacteria and fungi.

Uses

Used in Pharmaceutical Industry:
6-CHLORO-3,4-DIMETHYL-2-NITROPHENOL is used as an active ingredient in various pharmaceutical products for its strong antimicrobial properties. It is particularly effective in hand soaps and surgical scrubs, where it helps to reduce the spread of infections and maintain a hygienic environment.
Used in Personal Care Industry:
In the personal care industry, 6-CHLORO-3,4-DIMETHYL-2-NITROPHENOL is used as a key component in hand sanitizers and wound-care products. Its ability to eliminate a broad range of bacteria and fungi makes it an essential element in promoting skin health and preventing infections.
Used in Antimicrobial Coatings:
6-CHLORO-3,4-DIMETHYL-2-NITROPHENOL is utilized as an antimicrobial agent in coatings for various surfaces, such as medical equipment and hospital surfaces. This application helps to minimize the risk of hospital-acquired infections and ensures a cleaner, safer environment for patients and healthcare professionals.
Used in Textile Industry:
6-CHLORO-3,4-DIMETHYL-2-NITROPHENOL is also used in the textile industry to create antimicrobial fabrics. These fabrics are beneficial in producing clothing and bedding with enhanced hygiene properties, particularly for healthcare settings and personal use.
Used in Cosmetic Industry:
In the cosmetic industry, 6-CHLORO-3,4-DIMETHYL-2-NITROPHENOL is employed as a preservative in various cosmetic products. Its antimicrobial activity helps to prevent the growth of bacteria and fungi, thereby extending the shelf life and maintaining the quality of cosmetics.
Used in Veterinary Medicine:
6-CHLORO-3,4-DIMETHYL-2-NITROPHENOL is used in veterinary medicine as an antiseptic and disinfectant for treating wounds and infections in animals. Its broad-spectrum antimicrobial action ensures the effective management of various bacterial and fungal infections in veterinary practice.

Check Digit Verification of cas no

The CAS Registry Mumber 74098-29-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,0,9 and 8 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 74098-29:
(7*7)+(6*4)+(5*0)+(4*9)+(3*8)+(2*2)+(1*9)=146
146 % 10 = 6
So 74098-29-6 is a valid CAS Registry Number.
InChI:InChI=1/C8H8ClNO3/c1-4-3-6(9)8(11)7(5(4)2)10(12)13/h3,11H,1-2H3

74098-29-6SDS

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 6-chloro-3,4-dimethyl-2-nitrophenol

1.2 Other means of identification

Product number -
Other names 6-chloro-3,4-dimethyl-2-nitro-phenol

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:74098-29-6 SDS

74098-29-6Relevant articles and documents

Synthesis and isomerization of biindolinones from Collybia peronata and Tricholoma scalpturatum

Stachel, Shawn J.,Nilges, Mark,Van Vranken, David L.

, p. 4756 - 4762 (2007/10/03)

Peronatins A and B and 7,7'-dimethoxyperonatin B, originally isolated from the damaged fruiting bodies of Collybia peronata and Tricholoma scalpturatum, have been synthesized by oxidative dimerization of 2- alkylindoles. The conversion of peronatin A to peronatin B was shown to be catalyzed by Bronsted acids in chloroform solution and inhibited by triethylamine, implicating a retro-Mannich/Mannich isomerization pathway under these conditions. Attempts to identify or trap out radical or ionic intermediates were unsuccessful.

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