2666-53-7

Basic information

• Product Name: 2,4,6-TRIBROMOPHENOLSODIUMSALT
• Synonyms: 2,4,6-TRIBROMOPHENOLSODIUMSALT;SODIUM2,4,6-TRIBROMOPHENATE;SODIUMTRIBROMOPHENATE;Sodium 2,4,6-tribromophenolate
• CAS NO: 2666-53-7
• Molecular Formula: C₆H₂Br₃O*Na
• Molecular Weight: 353.79
• Mol File: 2666-53-7.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 286.8°Cat760mmHg
• Flash Point: 109.7°C
• Appearance: /
• Density: g/cm³
• Vapor Pressure: 0.0015mmHg at 25°C
• CAS DataBase Reference: 2,4,6-TRIBROMOPHENOLSODIUMSALT(CAS DataBase Reference)
• NIST Chemistry Reference: 2,4,6-TRIBROMOPHENOLSODIUMSALT(2666-53-7)
• EPA Substance Registry System: 2,4,6-TRIBROMOPHENOLSODIUMSALT(2666-53-7)

Safety Data

• Hazardous Substances Data: 2666-53-7(Hazardous Substances Data)

Usage

General Description

2,4,6-tribromophenolsodiumsalt is a chemical compound with the formula C6H2Br3O2Na. It is a member of the organobromine class of chemicals and is commonly used as a flame retardant in various products. The compound is soluble in water and often used in the production of flame-retardant materials such as textiles, plastics, and foam. 2,4,6-tribromophenolsodiumsalt works by reducing the flammability of these materials and is often used in combination with other flame retardants to enhance its effectiveness. However, concerns have been raised about its potential impact on human health and the environment, leading to restrictions in its use in some regions.

InChI:InChI=1/C6H3Br3O.Na/c7-3-1-4(8)6(10)5(9)2-3;/h1-2,10H;/q;+1/p-1

Upstream product

• 118-79-6 2,4,6-tribromophenol 
• 108-95-2 phenol 
• 78165-03-4 C₆H₂Br₃O 

Downstream Products

• 84998-84-5 (2,4,6-tribromo-phenoxy)-acetic acid 
• 201160-26-1 (2,4,6-tribromo-phenoxy)-acetone 
• 3278-89-5 1,3,5-tribromo-2-prop-2-enoxybenzene 
• 285981-78-4 diamminebis(2,4,6-tribromophenolato-O)copper(II) 
• 14711-10-5 N-Chlor-iminokohlensaeure-bis-<2,4,6-tribromphenylester> 
• 20244-60-4 2,4,4-tribromo-6-chloro-cyclohexa-2,5-dienone 
• 134145-76-9 1-Carbazol-9-yl-2-(2,4,6-tribromo-phenoxy)-propan-1-one 
• 134145-68-9 1-Carbazol-9-yl-2-(2,4,6-tribromo-phenoxy)-ethanone 
• 139554-52-2 2-(2,4,6-Tribromo-phenoxy)-propionyl chloride 
• 39784-12-8 2,4,6-tribromophenoxyacetyl chloride 
• 4641-30-9 2-(2,4,6-tribromo-phenoxy)-propionic acid 
• 68577-54-8 4-Phenyl-2,2,6-tris-(2,4,6-tribromo-phenoxy)-2λ⁵-[1,3,5,2]triazaphosphinine 
• 14711-08-1 Iminokohlensaeure-bis-<2,4,6-tribromphenylester> 
• 607-99-8 2,4,6-tribromoanisole 

Relevant articles and documents

Synthesis method of beraprost sodium intermediate

The invention relates to a synthesis method of a beraprost sodium intermediate I. Cyclopentene and N-bromosuccinimide (NBS) are subjected to a free radical reaction to obtain dibromocyclopentene, anda safer solvent is used for replacing solvents such as carbon tetrachloride and benzene; during preparation of sodium tribromophenolate, sodium hydroxide and other alkalis are used for replacing sodium hydride; 3, 5-bis (2, 4, 6-tribromophenoxy) cyclopentene is directly prepared from generated dibromocyclopentene and 2, 4, 6-tribromophenol sodium through interaction by a'one-pot boiling 'method. The improved reaction conditions are milder, the environment is more friendly, and industrial production is facilitated.

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.