Hexabromobenzene

Hexabromobenzene
Names
Preferred IUPAC name
Hexabromobenzene
Other names
  • Perbromobenzene
  • HBB
Identifiers
3D model (JSmol)
ChEMBL
ChemSpider
ECHA InfoCard 100.001.613 Edit this at Wikidata
EC Number
  • 201-773-9
UNII
UN number 3077
  • InChI=1S/C6Br6/c7-1-2(8)4(10)6(12)5(11)3(1)9
    Key: CAYGQBVSOZLICD-UHFFFAOYSA-N
  • InChI=1/C6Br6/c7-1-2(8)4(10)6(12)5(11)3(1)9
    Key: CAYGQBVSOZLICD-UHFFFAOYAA
  • C1(=C(C(=C(C(=C1Br)Br)Br)Br)Br)Br
Properties
C6Br6
Molar mass 551.490 g·mol−1
Appearance Monoclinic needles or white powder.[1]
Odor Odorless[2]
Melting point 327 °C (621 °F; 600 K)[2]
0.16x10−3 mg/L (insoluble)[1]
Solubility Slightly soluble in Ethanol, Diethyl ether[3]
Solubility in Acetic acid Soluble[3]
Solubility in Benzene 10%[4]
Solubility in Chloroform 10%[4]
Solubility in Petroleum ether 10%[4]
log P 6.07[1]
Hazards
GHS labelling:[2]
GHS07: Exclamation mark
Danger[2]
H302, H312, H315, H319, H332, H335, H413[1]
P261, P264, P270, P271, P280, P301+P312, P302+P352, P304+P312, P304+P340, P305+P351+P338, P312, P321, P322, P330, P332+P313, P362, P363, P403+P233, P405, P501[1]
NFPA 704 (fire diamond)
NFPA 704 four-colored diamondHealth 2: Intense or continued but not chronic exposure could cause temporary incapacitation or possible residual injury. E.g. chloroformFlammability 0: Will not burn. E.g. waterInstability 0: Normally stable, even under fire exposure conditions, and is not reactive with water. E.g. liquid nitrogenSpecial hazards (white): no code
2
0
0
Safety data sheet (SDS) LCSS 6905
Related compounds
Related compounds
Hexafluorobenzene
Hexachlorobenzene
Hexaiodobenzene
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Hexabromobenzene (HBB) is an organobromine compound with the formula C6Br6. It features a central benzene ring with sixbromine substituents. Hexabromobenzene is a white powder that is not soluble in water but is soluble in ethanol, ether, and benzene. Its bromine content is above 86%.[5]

Preparation

It can be prepared by the reaction of benzene with 6 equivalents of bromine (Br2) in the presence of heat and UV light:[citation needed]

C6H6 + 6 Br2 → C6Br6 + 6 HBr

The reaction produces six equivalents of hydrogen bromide.

Uses

Hexabromobenzene has seen use in high voltage capacitors as a flame retardant.[6]

Hexabromobenzene finds extensive use as a fire retardant additive in a range of materials including plastics, paper, and electrical goods, where it serves as a top-tier flame retardant. It was introduced to replace traditional organobromine fire retardants such as polybrominated derivatives of diphenyl ethers and biphenyls.[7] With a high melting point of 327 °C and a high bromide content of 86%, HBB significantly enhances the fire safety of these materials.[8] Iits widespread application also leads to its dispersion in the environment.

Metabolism

Hexabromobenzene was used in a study investigating its metabolic fate in female rats, wherein the substance was orally administered at doses of 16.6 mg/kg body weight every other day for a span of 2 weeks. Analysis of the rats' excreta revealed the presence of various metabolites, including unchanged HBB, pentabromobenzene, as well as oxygen- and sulfur-containing compounds.[9]

Dangers

Hexabromobenzene poses significant dangers due to its toxicity profile as classified by the GHS (Globally Harmonized System of Classification and Labeling of Chemicals). Classified as GHS07, HBB exhibits acute toxicity via oral, dermal, and inhalation routes, categorizing it under category 4 for this hazard. Additionally, it induces skin and eye irritation, classified under category 2 for both. Moreover, HBB is known to cause skin sensitization (category 1) and specific target organ toxicity upon single exposure (category 3), with the respiratory system being the primary target organ.[10]

The acute toxicity of brominated benzenes decreases with an increase in the number of bromine atoms in the molecule.[11] However, the potential for necrotic changes varies based on the position of these bromine atoms within the molecule. There are severe health risks associated with HBB exposure, warranting careful handling and stringent safety measures in its use and management.[10]

References

  1. ^ a b c d e CID 6905 from PubChem
  2. ^ a b c d Record in the GESTIS Substance Database of the Institute for Occupational Safety and Health
  3. ^ a b Weast, R.C. (1979). Handbook of Chemistry and Physics (60 ed.). Boca Raton, Florida: CRC Press Inc. p. C-165. ISBN 9780849315565.
  4. ^ a b c Weast, Robert C.; Astle, Melvin J. (1985). CRC Handbook of Data On Organic Compounds. Vol. 1. Boca Raton, Florida: CRC Press Inc. p. 176. ISBN 9780849304002.
  5. ^ PubChem. "Hexabromobenzene". pubchem.ncbi.nlm.nih.gov. Retrieved 2024-02-11.
  6. ^ US Grant 6909590, Tsukasa Sato, Isao Fujiwara, Makoto Morita, Kenichi Horikawa, "High voltage capacitor and magnetron", published 2004-08-09, issued 2005-06-21, assigned to TDK Corp 
  7. ^ Hou, Rui; Lin, Lang; Li, Hengxiang; Liu, Shan; Xu, Xiangrong; Xu, Yiping; Jin, Xiaowei; Yuan, Yong; Wang, Zijian (2021). "Occurrence, bioaccumulation, fate, and risk assessment of novel brominated flame retardants (NBFRS) in aquatic environments — A critical review". Water Research. 198. Bibcode:2021WatRe.19817168H. doi:10.1016/j.watres.2021.117168. PMID 33962238.
  8. ^ "Premium 98% Pure Hexabromobenzene for Enhanced Fire Resistance & Versatility". Procurenet Limited. Retrieved 2024-02-11.
  9. ^ Koss, G; Doring, H; Wurminghausen, B; Koransky, W (November 1982). "Metabolic fate of hexabromobenzene in rats". Toxicology Letters. 14 (1–2): 69–77. doi:10.1016/0378-4274(82)90011-X.
  10. ^ a b "Hexabromobenzene". Sigma-Aldrich. August 27, 2023. Archived from the original on January 13, 2024. Retrieved February 3, 2024.
  11. ^ Peng, Anping; Gao, Hu; Wang, Huimin; Wang, Yi; Chen, Zeyou (July 2023). "Influence of organic cosolvents on hexabromobenzene degradation in solution by montmorillonite-templated subnanoscale zero-valent iron". Environmental Research. 229: 115986. Bibcode:2023ER....22915986P. doi:10.1016/j.envres.2023.115986. PMID 37100367.

 

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