2,4,6-Tribromofenol

2,4,6-Tribromofenol
Nazivi
	IUPAC naziv 2,4,6-Tribromofenol
	Drugi nazivi Tribromofenol; 2,4,6-TBP; TBP
Identifikacija
CAS broj	118-79-6 ;
3D model (Jmol)	interaktivna slika;
ChEBI	CHEBI:47696 ;
ChemSpider	1438 ;
DrugBank	DB02417 ;
ECHA InfoCard	100.003.890
KEGG	C14454 ;
PubChem C ID	1483;
	SMILES Brc1cc(Br)cc(Br)c1O; ; ; ; ; ;
Svojstva
Hemijska formula	C6H3Br3O
Molarna masa	330,80 g·mol−1
Agregatno stanje	Bele igle ili prizme
Tačka topljenja	95.5 °C
Tačka ključanja	244 °C; 286 °C
Rastvorljivost u vodi	Malo rastvoran; 59-61 mg/L
Opasnosti
	Letalna doza ili koncentracija (LD, LC):
LD50 (LD50)	2000 mg/kg (pacov, oralno)
	Ukoliko nije drugačije napomenuto, podaci se odnose na standardno stanje materijala (na 25 °C [77 °F], 100 kPa).
	verifikuj (šta je ?)
	Reference infokutije

2,4,6-Tribromofenol (TBP) je brominisani derivat fenola. On se koristi kao fungicid, prezervativ drveta, i kao intermedijer u pripremi sredstava za gašenje požara.

Produkcija

Mada je prirodni TBP identifikovan u okeanskim sedimentima kao metabolit morske faune,^[7] komercijalni produkt se priprema veštačkim putem. Po procenama iz 2001. svetska proizvodnja nadmašuje 9.500 tona godišnje.^[6] TBP se može pripremiti kontrolisanom reakcijom elementrnog broma i fenola:^[5]

Reference

^ Joanne Wixon; Douglas Kell (2000). „Website Review: The Kyoto Encyclopedia of Genes and Genomes — KEGG”. Yeast. 17 (1): 48—55. doi:10.1002/(SICI)1097-0061(200004)17:1<48::AID-YEA2>3.0.CO;2-H.
^ Li Q, Cheng T, Wang Y, Bryant SH (2010). „PubChem as a public resource for drug discovery.”. Drug Discov Today. 15 (23-24): 1052—7. PMID 20970519. doi:10.1016/j.drudis.2010.10.003. уреди
^ Evan E. Bolton; Yanli Wang; Paul A. Thiessen; Stephen H. Bryant (2008). „Chapter 12 PubChem: Integrated Platform of Small Molecules and Biological Activities”. Annual Reports in Computational Chemistry. 4: 217—241. doi:10.1016/S1574-1400(08)00012-1.
^ ^а ^б ^в ^г ^д Milne, G. W. A., ур. (2010). „3851: Tribromophenol”. Gardner's Commercially Important Chemicals: Synonyms, Trade Names, and Properties. стр. 632. ISBN 978-0-471-73518-2.
^ ^а ^б Merck Index, 11th Edition, 9526
^ ^а ^б Concise International Chemical Assessment Document 66: 2,4,6-Tribromophenol and Other Simple Brominated Phenols, International Programme on Chemical Safety
^ Fielman KT, Woodin SA, Lincoln DE (2001). „Polychaete indicator species as a source of natural halogenated organic compounds in marine sediments”. Environmental Toxicology and Chemistry. 20 (4): 738—747. PMID 11345448. doi:10.1002/etc.5620200407.

[1] Joanne Wixon; Douglas Kell (2000). „Website Review: The Kyoto Encyclopedia of Genes and Genomes — KEGG”. Yeast. 17 (1): 48—55. doi:10.1002/(SICI)1097-0061(200004)17:1<48::AID-YEA2>3.0.CO;2-H.

[2] Li Q, Cheng T, Wang Y, Bryant SH (2010). „PubChem as a public resource for drug discovery.”. Drug Discov Today. 15 (23-24): 1052—7. PMID 20970519. doi:10.1016/j.drudis.2010.10.003. уреди

[3] Evan E. Bolton; Yanli Wang; Paul A. Thiessen; Stephen H. Bryant (2008). „Chapter 12 PubChem: Integrated Platform of Small Molecules and Biological Activities”. Annual Reports in Computational Chemistry. 4: 217—241. doi:10.1016/S1574-1400(08)00012-1.

[Gardner-4] а ^б ^в ^г ^д Milne, G. W. A., ур. (2010). „3851: Tribromophenol”. Gardner's Commercially Important Chemicals: Synonyms, Trade Names, and Properties. стр. 632. ISBN 978-0-471-73518-2.

[Merck-5] а ^б Merck Index, 11th Edition, 9526

[Inchem-6] а ^б Concise International Chemical Assessment Document 66: 2,4,6-Tribromophenol and Other Simple Brominated Phenols, International Programme on Chemical Safety

[7] Fielman KT, Woodin SA, Lincoln DE (2001). „Polychaete indicator species as a source of natural halogenated organic compounds in marine sediments”. Environmental Toxicology and Chemistry. 20 (4): 738—747. PMID 11345448. doi:10.1002/etc.5620200407.

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