13075-01-9

Basic information

• Product Name: 1,2,4-tribromo-3,5,6-trichlorobenzene
• Synonyms: 1,2,4-Tribromo-3,5,6-trichlorobenzene; benzene, 1,2,4-tribromo-3,5,6-trichloro-
• CAS NO: 13075-01-9
• Molecular Formula: C₆Br₃Cl₃
• Molecular Weight: 418.1352
• Mol File: 13075-01-9.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 376.1°C at 760 mmHg
• Flash Point: 192.9°C
• Density: 2.405g/cm³
• Vapor Pressure: 1.61E-05mmHg at 25°C
• Refractive Index: 1.657
• CAS DataBase Reference: 1,2,4-tribromo-3,5,6-trichlorobenzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2,4-tribromo-3,5,6-trichlorobenzene(13075-01-9)
• EPA Substance Registry System: 1,2,4-tribromo-3,5,6-trichlorobenzene(13075-01-9)

Safety Data

• Hazardous Substances Data: 13075-01-9(Hazardous Substances Data)

Usage

Structure

Three bromine atoms and three chlorine atoms are attached to a benzene ring.

Halogenated compound

Highly halogenated organic compound.

Primary use

Flame retardant and in the production of various industrial products.

Industrial applications

Electrical and electronic devices, textiles, and plastics.

Thermal stability

High thermal stability and resistance to degradation.

Environmental concern

Identified as a persistent organic pollutant.

Bioaccumulation

Potential to bioaccumulate in organisms.

Toxicity

Toxicity to aquatic life.

Regulatory status

Use has been restricted in several countries to minimize environmental and human health impact.

Upstream product

• 103038-81-9 2-tert-butyl-1,3,4-trichloro-benzene 
• 120-82-1 1,2,4-Trichlorobenzene 
• 103038-80-8 1-tert-butyl-2,4,5-trichloro-benzene 

Downstream Products

• 30936-28-8 3,5,6-Trichlor-trimellitonitril 

Relevant articles and documents

ORGANIC LIGHT-EMITTING DIODE MATERIALS

Described herin are molecules for use in organic light emitting diodes. Example molecules comprise at least one acceptor moiety A, at least one donor moiety D, and optionally one or more bridge moieties B. Each moiety A is covalently attached to either the moiety B or the moeity D, each moiety D is covalently attached to either the moeity B or the moeity A, and each B is covalently attached to at least one moiety A and at least one moiety D. Values and preferred values of moieties A, D and B are defined herein.

PERBROMINATION OF BENZENE AND SOME OF ITS DERIVATIVES

Perbrominated compounds - pentabromophenol, hexabromobenzene, pentabromotoluene, polychlorobromobenzenes, and decabromodiphenyl ether - have been obtained.Substitution bromination has been discovered in treating diphenyl sulfoxide, diphenyl sulfide, diphenylmethane, diphenyl oxide, and benzophenone with excess bromine in the presence of AlBr3.A series of ethers and esters of pentabromophenol have been obtained; their hydrolysis has been carried out.A negative influence of ferric halides has been discovered in exhaustive bromination of aromatic compounds.