Pentabromobenzyl acrylate
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| Names | |
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| IUPAC name
(2,3,4,5,6-pentabromophenyl)methyl prop-2-enoate | |
| Identifiers | |
3D model (JSmol) |
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| ChemSpider | |
| ECHA InfoCard | 100.056.134 |
| EC Number |
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PubChem CID |
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| UNII | |
CompTox Dashboard (EPA) |
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| Properties | |
| C10H5Br5O2 | |
| Molar mass | 556.668 g·mol−1 |
| Hazards | |
| GHS labelling:[1] | |
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| Warning | |
| H319, H413 | |
| P264+P265, P273, P280, P305+P351+P338, P337+P317, P501 | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references | |
Pentabromobenzyl acrylate (abbreviated as PBB-Acr)[2] is an organic compound used as a reactive flame retardant in polybutylene terephthalate, polyethylene terephthalate, and acrylonitrile butadiene styrene polymers.[3][4]
References
- ↑ PubChem. "2-Propenoic acid, (2,3,4,5,6-pentabromophenyl)methyl ester". pubchem.ncbi.nlm.nih.gov. Retrieved 2026-05-23.
- ↑ Åke Bergman; et al. (2012), "A novel abbreviation standard for organobromine, organochlorine and organophosphorus flame retardants and some characteristics of the chemicals", Environment International, vol. 49, pp. 57–82, Bibcode:2012EnInt..49...57B, doi:10.1016/j.envint.2012.08.003, PMC 3483428, PMID 22982223
- ↑ Adrian Covaci, Stuart Harrad, Mohamed A.-E. Abdallah, Nadeem Ali, Robin J. Law, Dorte Herzke, Cynthia A. de Wit (February 2011), "Novel brominated flame retardants: a review of their analysis, environmental fate and behaviour", Environment International, vol. 37, no. 2, pp. 532–556, Bibcode:2011EnInt..37..532C, doi:10.1016/j.envint.2010.11.007, PMID 21168217
{{citation}}: CS1 maint: multiple names: authors list (link) - ↑ EFSA Panel on Contaminants in the Food Chain (October 2012), "Scientific Opinion on Emerging and Novel Brominated Flame Retardants (BFRs) in Food", EFSA Journal, vol. 10, no. 10, doi:10.2903/j.efsa.2012.2908

