57730-98-0

Basic information

• Product Name: 2,4,6-Tribromothiophenol
• Synonyms: 2,4,6-tribromothiophenol;BENZENETHIOL 2,4,6-TRIBROMINE;2,4,6-Tribromobenzenethiol;2,4,6-Tribromothioph
• CAS NO: 57730-98-0
• Molecular Formula: C₆H₃Br₃S
• Molecular Weight: 346.87
• Mol File: 57730-98-0.mol

Chemical Properties

• Melting Point: 115.5-115.9 °C
• Boiling Point: 328.8°Cat760mmHg
• Flash Point: 152.7°C
• Appearance: /
• Density: 2.303g/cm³
• Vapor Pressure: 0.000354mmHg at 25°C
• Refractive Index: 1.689
• PKA: 4.63±0.50(Predicted)
• CAS DataBase Reference: 2,4,6-Tribromothiophenol(CAS DataBase Reference)
• NIST Chemistry Reference: 2,4,6-Tribromothiophenol(57730-98-0)
• EPA Substance Registry System: 2,4,6-Tribromothiophenol(57730-98-0)

Safety Data

• Hazardous Substances Data: 57730-98-0(Hazardous Substances Data)

Usage

Uses

Used in Flame Retardant Applications:
2,4,6-Tribromothiophenol is used as a flame retardant for enhancing the fire resistance of various materials. It is incorporated into polymers, plastics, and other materials to improve their ability to withstand combustion.
Used in Polymer and Plastic Industries:
In the polymer and plastic industries, 2,4,6-Tribromothiophenol is used as an additive to confer flame-retardant properties to the final products, ensuring they meet safety standards and reducing the risk of fire-related incidents.
Environmental and Health Considerations:
It is important to consider the potential environmental and health impacts of 2,4,6-Tribromothiophenol, as it has raised concerns due to its chemical nature. As a result, its usage is regulated in some countries to mitigate any adverse effects on the environment and human health.

InChI:InChI=1/C6H3Br3S/c7-3-1-4(8)6(10)5(9)2-3/h1-2,10H

Upstream product

• 61268-35-7 O-(2,4,6-tribromophenyl)-N,N-dimethylthiocarbamate 
• 118-79-6 2,4,6-tribromophenol 
• 857782-13-9 dithiocarbonic acid S,S'-bis-(2,4,6-tribromo-phenyl ester) 

Downstream Products

• 62601-13-2 1,3,5-Tribromo-2-chloromethylsulfanyl-benzene 

Relevant articles and documents

N-(5,7-dibromo-1,3-benzoxathiol-2-ylidene)-N-methylmethanaminium bromide, N-(5,7-diiodo-1,3-benzoxathiol-2-ylidene)-N-methylmethanaminium iodide and their preparation

N-(5,7-Dibromo-1,3-benzoxathiol-2-ylidene)-N-methylmethanaminium bromide and the analogous diodo iodide, new compounds, are prepared by the thermal rearrangement of O-(2,4,6-tribromophenyl)-N,N-dimethylthiocarbamate and O-(2,4,6-triiodophenyl)-N,N-dimethy

Pesticidal compositions containing phosphoric esters and divalent sulphur compounds

Pesticidal composition comprising: a pesticidal, phosphoric ester the molecule of which has at least one alkyl group of 1 to 3 carbon atoms, 0.05 to 10% of an agent stabilizing the said ester against decomposition by protonisation, together with adjuvants characterized in that the stabilizing agent comprises at least one sulphur compound containing per molecule at least one divalent sulphur atom of which one valence is bonded to an atom chosen from sulphur, carbon, nitrogen, hydrogen, and metals capable of giving a salt, the other valence being bonded to an atom chosen from hydrogen, the carbon atom already noted, a second carbon atom, the nitrogen atom already noted, a second nitrogen atom, the metal atom already noted in the case of a metal of valence greater than one, a second atom of metal and oxygen when the first valence is not attached to an atom of hydrogen, the proportion of sulphur calculated with reference to the weight of the sulphur compound being between 5 and 99%. Process for stabilizing a phosphoric ester of which the molecule possesses at least one alkyl group containing 1 to 3 carbon atoms characterized in that there is added to the phosphoric ester or to a mixture which contains it, 0.05 to 10% calculated on the weight of the phosphoric acid ester of an agent capable of stabilizing the said phosphoric ester against protonisation and comprising at least one sulphur compound such as that defined thereupon.