29426-78-6

Basic information

• Product Name: 2-bromo-4-[2-(3-bromo-4-hydroxy-phenyl)propan-2-yl]phenol
• Synonyms: 2-bromo-4-[2-(3-bromo-4-hydroxy-phenyl)propan-2-yl]phenol;2,2-Bis(3-bromo-4-hydroxyphenyl)propane
• CAS NO: 29426-78-6
• Molecular Formula: C₁₅H₁₄Br₂O₂
• Molecular Weight: 386.08
• Mol File: 29426-78-6.mol
• Article Data: 10

Chemical Properties

• Boiling Point: 409.6°Cat760mmHg
• Flash Point: 201.5°C
• Appearance: /
• Density: 1.664g/cm³
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 2-bromo-4-[2-(3-bromo-4-hydroxy-phenyl)propan-2-yl]phenol(CAS DataBase Reference)
• NIST Chemistry Reference: 2-bromo-4-[2-(3-bromo-4-hydroxy-phenyl)propan-2-yl]phenol(29426-78-6)
• EPA Substance Registry System: 2-bromo-4-[2-(3-bromo-4-hydroxy-phenyl)propan-2-yl]phenol(29426-78-6)

Safety Data

• Hazardous Substances Data: 29426-78-6(Hazardous Substances Data)

Usage

General Description

2-bromo-4-[2-(3-bromo-4-hydroxy-phenyl)propan-2-yl]phenol is a chemical compound that belongs to the class of brominated phenols. It is a highly reactive and potentially toxic compound that can be used as a disinfectant, antiseptic, and antimicrobial agent. Its molecular structure consists of a phenol group substituted with bromine atoms and a propyl group. The compound has been studied for its potential applications in pharmaceuticals, agrochemicals, and industrial processes, but its use is limited due to its potential toxicity and environmental impact. It is important to handle this compound with caution and adhere to safety protocols when working with it.

Upstream product

• 80-05-7 BPA 

Downstream Products

• 18811-78-4 4,4'-(propane-2,2-diyl)bis(benzene-1,2-diol) 
• 945548-25-4 2,2-bis(4-methoxy-3-bromophenyl)propane 

Relevant articles and documents

Synthesis and Toxicity of Halogenated Bisphenol Monosubstituted-Ethers: Establishing a Library for Potential Environmental Transformation Products of Emerging Contaminant

As an important branch of halogenated bisphenol compounds, the halogenated bisphenol monosubstituted-ether compounds have received a lot of attention in environmental health science because of their toxicity and variability. In this study, a synthetic method for bisphenol monosubstituted-ether byproduct libraries was developed. By using the versatile and efficient method, tetrachlorobisphenol A, tetrabromobisphenol A, and tetrabromobisphenol S monosubstituted alkyl-ether compounds were accessed in 39–82 % yield. Subsequently, the cytotoxicity of 27 compounds were screened using three different cell lines (HepG2, mouse primary astrocytes and Chang liver cells). Compound 2,6-dibromo-4-[3,5-dibromo-4-(2-hydroxyethoxy)benzene-1-sulfonyl]phenol was more toxic than other compounds in various cells, and the sensitivity of this compound to the normal hepatocytes and cancer cells was inconsistent. The compounds 2,6-dichloro-4-(2-{3,5-dichloro-4-[(prop-2-en-1-yl)oxy]phenyl}propan-2-yl)phenol and 2,6-dibromo-4-(2-{3,5-dibromo-4-[(prop-2-en-1-yl)oxy]phenyl}propan-2-yl)phenol were the most toxic to HepG2 cells, and most of the other compounds inhibited cell proliferation. Moreover, typical compounds were also reproductive and developmental toxic to zebrafish embryos at different concentrations. The synthetic byproduct libraries could be used as pure standard compounds and applied in research on environmental behavior and the transformation of halogenated flame retardants.

MEDICAL DEVICE USING SULFONATED NEUTRALIZED POLYMERS WITH REDUCED ADHESION OF BIOLOGICAL FLUIDS

A medical article having neutralized sulfonic acid groups on its surface, is disclosed. The article has reduced interaction with biological fluids such as insulin, human growth hormone and human serum albumin.

Method for manufacturing bisphenol

A method for manufacturing bisphenol by reacting phenols and ketones, characterized (1) in that an alkali metal compound and/or alkaline earth metal compound is added to bisphenol obtained by reacting a phenol and a ketone, and (2) in that the basicity of the bisphenol is adjusted so as to be equivalent to an amount of 1 × 10-8to 1 × 10-6moles of bisphenol as disodium salt with respect to 1 mole of bisphenol provides a bisphenol in which there is no residue of the organic catalysts ordinarily used in manufacturing bisphenol, so that byproducts are not produced during purification, allowing bisphenol with outstanding color tone, thermal resistance, etc., to be obtained.