2,4,6-TRIBROMOPHENOL

PRODUCT IDENTIFICATION

CAS NO. 118-79-6

2,4,6-TRIBROMOPHENOL

EINECS NO. 204-278-6
FORMULA Br3C6H2OH
MOL WT. 330.82

H.S. CODE

2908.19.6000

 

 

TOXICITY

Oral rat LD50: 200 mg/kg

SYNONYMS Tribromophenol; Bromol; Bromkal Pur 3; 三溴苯酚; Xeroform;
SMILES c1(c(cc(Br)cc1Br)Br)O

CLASSIFICATION

Flame Retardant, Fungicide, Organobromide

EXTRA NOTES

TSCA Flag T [Subject to the Section 4 test rule under TSCA]

PHYSICAL AND CHEMICAL PROPERTIES

PHYSICAL STATE white to pink powder

MELTING POINT

92 - 94 C
BOILING POINT 282 - 290 C
SPECIFIC GRAVITY 2.55

SOLUBILITY IN WATER

Slightly soluble
VAPOR DENSITY 11.4
pKa 6.8 (Dissociation Constant at 20 C)
log Pow 4.13 (Octanol-water)
VAPOR PRESSURE 3.03E-04 (mmHg at 25 C)
HENRY LAW CONSTANT 3.55E-08 (atm-m3/mole at 25 C)
OH RATE CONSTANT 4.75E-13 (cm3/molecule-sec at 25 C Atmospheric )

AUTOIGNITION

 

NFPA RATINGS

Health: 1; Flammability: ; Reactivity: 0

REFRACTIVE INDEX

 

FLASH POINT

178 C

STABILITY Stable under ordinary conditions

EXTERNAL LINKS & GENERAL DESCRIPTION

Wikipedia Linking

Material Safety Data Sheet

Google Scholar Search

http://www.inchem.org/
The production volume of 2,4,6-tribromophenol was estimated at approximately 2,500 t/year in Japan and 9,500 t/year world-wide in 2001. This substance is produced in a closed system. This substance is used almost entirely as a chemical intermediate to make a flame retardant or directly as a flame retardant. The way to use this substance as a flame retardant is called "capping" i.e. the terminal -OH group of a polymer is capped with 2,4,6-tribromophenol which is then covalently bound to the polymer. The reaction occurs during polymerization of oxirane to form 2,4,6-tribromophenoxy-ether. Consequently, the resulting polymer becomes flame retardant/resistant. The presence of the free substance itself in the polymer would give the resin a stinking odor because of the sublimating property of the substance and the resin would not be of commercial value. The potential for release of this substance from resins “capped" with it are not higher than the potential for release of 2,4,6-tribromophenol from polymers added with flame retardants derived from this substance. Other than that, antiseptic and germicide use (e.g., in pharmaceutical prepns) is reported [Danish EPA, 2000]. However, the amount is too small to be detected by the producer of the chemical.

Local: Flame retardant in epoxy, polyurethane, plastics, paper and textiles. Fire extinguishing media. 2,4,6-Tribromophenol is used also as an flame retardant in epoxy, polyurethane, plastics, paper, textiles and others. It can be combined with a synergist such as antimony trioxide for maximum flame retardant performance. Tribromophenol may also be used as an intermediate for the production of other commercial flame retardants and fire extinguishing media. It can be used as an antiseptic agent.

SALES SPECIFICATION

APPEARANCE

white to pink powder

BROMINE CONTENT

71.5% min

MELTING POINT

90 C min

LOSS ON DRYING

0.5% max

TRANSPORTATION
PACKING 25kgs in bag
HAZARD CLASS

6.1 (Packing group : III)

UN NO. 2811
GENERAL DESCRIPTION OF FLAME RETARDANT AGENT

Flame Retardant are substances that can be chemically inserted into the polymer molecule or be phisically blended in polymers after polymerization to suppress, reduce, delay or modify the propagation of a flame through a plastic materials. There are several classes of flame retardants; Halogenated Hydrocarbons (Chlorine and Bromine containing compounds and reactive flame retardants), Inorganic flame retardants ( Boron compounds, Antimony oxides, Aluminium Hydroxide, molybdenum compounds, zinc and magnesium oxides ), Phosphorous containing compounds (Organic phosphate esters, phosphates, halogenated phosphorus compounds and inorganic phosphorus containing salts).

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