3784-03-0

Basic information

• Product Name: Sodium 2,4,6-trichlorophenolate
• Synonyms: 2,4,6-TRICHLOROPHENOL SODIUM SALT HYDRATE;1-Sodiooxy-2,4,6-trichlorobenzene;FREE SAMPLE NCV 2,4,6-TRICHLORP PHENOL;2,4,6-trichloro-phenosodiumsalt;2,4,6-TRICHLOROPHENOL SODIUM SALT;Sodium 2,4,6-trichlorophenolate;SODIUM TRICHLOROPHENATE;Phenol, 2,4,6-trichloro-, sodium salt
• CAS NO: 3784-03-0
• Molecular Formula: C₆H₂Cl₃O*Na
• Molecular Weight: 219.43
• EINECS: 223-246-2
• Product Categories: Phenoles and thiophenoles
• Mol File: 3784-03-0.mol

Chemical Properties

• Melting Point: 185 °C
• Boiling Point: 246 °C at 760 mmHg
• Flash Point: 95.9 °C
• Appearance: light yellow liquid
• Vapor Pressure: 0.0177mmHg at 25°C
• Storage Temp.: Sealed in dry,Room Temperature
• Solubility: soluble in Methanol
• Merck: 14,9644
• CAS DataBase Reference: Sodium 2,4,6-trichlorophenolate(CAS DataBase Reference)
• NIST Chemistry Reference: Sodium 2,4,6-trichlorophenolate(3784-03-0)
• EPA Substance Registry System: Sodium 2,4,6-trichlorophenolate(3784-03-0)

Safety Data

• Statements: 20/21/22-36/37/38
• Safety Statements: 26-36/37/39
• RIDADR: 2020
• HazardClass: 6.1(b)
• PackingGroup: III
• Hazardous Substances Data: 3784-03-0(Hazardous Substances Data)

Usage

Uses

Used in Cleaning Products:
Sodium 2,4,6-trichlorophenolate is used as a disinfectant and preservative for its ability to control microbial growth and inhibit the development of mold, mildew, and bacteria in cleaning products.
Used in Wood Preservation:
In the wood industry, sodium 2,4,6-trichlorophenolate is used as a preservative to protect wood from microbial decay and infestation, thereby extending its lifespan and maintaining its structural integrity.
Used in Leather Preservation:
Sodium 2,4,6-trichlorophenolate serves as a preservative in the leather industry to prevent the growth of mold and mildew, ensuring the durability and quality of leather goods.
Used in Textile Preservation:
This chemical compound is utilized in the textile industry as a preservative to protect fabrics from microbial damage, thus maintaining their appearance and functionality.

InChI:InChI=1/C6H3Cl3O.Na/c7-3-1-4(8)6(10)5(9)2-3;/h1-2,10H;/q;+1/p-1

Downstream Products

• 87-40-1 2,4,6-trichloroanisole 
• 53625-00-6 α-(2,4,6-trichloro-phenoxy)-isobutyric acid 
• 31836-18-7 2,4,6-trichlorophenyl chlorothionoformate 
• 778-83-6 2-(2,4,6-trichlorophenoxy)propanoic acid 
• 114133-84-5 N-ethyl-N'-methyl-diamidothiophosphoric acid O-(2,4,6-trichloro-phenyl ester) 
• 116401-94-6 ethyl-amidothiophosphoric acid O-ethyl ester-O'-(2,4,6-trichloro-phenyl ester) 
• 52200-07-4 (2,4,6-trichloro-phenoxysulfonyl)-carbamic acid methyl ester 
• 99848-00-7 (2,4,6-trichloro-phenoxymethyl)-phosphonic acid monoethyl ester 
• 101365-41-7 isopropyl-amidothiophosphoric acid O-ethyl ester-O'-(2,4,6-trichloro-phenyl ester) 
• 132982-56-0 (2,4,6-trichloro-phenoxy)-methanesulfonic acid 

Relevant articles and documents

Free Radical Combination Reactions Involving Phenoxyl Radicals

The rates of phenoxyl radical reactions with the superoxide anion radical, O2.-, a peroxyl radical, HOC(CH3)2CH2OO., and an alkyl radical, HOC(CH3)2CH2., in aqueous solution have been measured for 15 different phenoxyl radicals by means of pulse radiolysis.In addition, the one-electron reduction potentials of 10 phenoxyl radicals have been determined.The fraction of electron transfer in the reaction of phenoxyl radicals with O2.- was determined by analysis of γ-irradiated samples.The experimental data can be accommodated by the Marcus theory for electron transfer, with the reorganization energy λ0 = 155 kJ/mol for the reaction between O2.- and phenoxyl radicals.