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137715

Sigma-Aldrich

2,4,6-Tribromophenol

99%

Sinonimo/i:

1,3,5-Tribromo-2-hydroxybenzene, Bromol

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About This Item

Formula condensata:
Br3C6H2OH
Numero CAS:
118-79-6
Peso molecolare:
330.80
Beilstein:
776920
Numero CE:
204-278-6
Numero MDL:
MFCD00002150
Codice UNSPSC:
12352100
ID PubChem:
24848344
NACRES:
NA.22

Densità del vapore

11.4 (vs air)

Saggio

99%

P. eboll.

282-290 °C/746 mmHg (lit.)

Punto di fusione

90-94 °C (lit.)

Solubilità

water: soluble 0.007g/100ml at 25 °C
chloroform: soluble
diethyl ether: soluble
ethanol: soluble
methanol: soluble
methylene chloride: soluble

Stringa SMILE

Oc1c(Br)cc(Br)cc1Br

InChI

1S/C6H3Br3O/c7-3-1-4(8)6(10)5(9)2-3/h1-2,10H
BSWWXRFVMJHFBN-UHFFFAOYSA-N

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Descrizione generale

2,4,6-Tribromophenol undergoes oxidative degradation catalyzed by SiO2-supported iron(III)-5,10,15,20-tetrakis(4-carboxyphenyl) porphyrin. It is degraded by Bacillus sp.GZT strain via reductive bromination as major degradation pathway. It is a widely used brominated flame retardant.

Applicazioni

2,4,6-Tribromophenol was used in analysis of nonylphenol, nonylphenol monoethoxylate and octylphenol in sediment, water and fish tissue.

Pittogrammi

Exclamation markEnvironment
GHS07,GHS09

Avvertenze

Warning

Indicazioni di pericolo

H317,H319,H400

Classi di pericolo

Aquatic Acute 1 - Eye Irrit. 2 - Skin Sens. 1

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Certificati d'analisi (COA)

Cerca il Certificati d'analisi (COA) digitando il numero di lotto/batch corrispondente. I numeri di lotto o di batch sono stampati sull'etichetta dei prodotti dopo la parola ‘Lotto’ o ‘Batch’.

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Lye CM, et al.
Environmental Science & Technology, 33(7), 1009-1014 (1999)
Qianqian Zhu et al.
Journal of environmental science and health. Part A, Toxic/hazardous substances & environmental engineering, 48(13), 1593-1601 (2013-08-21)
Iron(III)-porphyrin complexes are generally regarded as green catalysts, since they mimic the catalytic center of cytochrome-P450 and widely used as green catalysts for degrading halogenated phenols in wastewater, such as landfill leachates. However, iron(III)-porphyrins are deactivated by self-oxidation in the
C Pizarro et al.
Journal of chromatography. A, 1217(49), 7630-7637 (2010-11-03)
A dispersive liquid-liquid microextraction (DLLME) method has been optimised for simultaneously extracting 2,4,6-trichloranisole (TCA), 2,3,4,6-tetrachloroanisole (TeCA), 2,4,6-tribromoanisole (TBA), pentachloroanisole (PCA), 2,4,6-trichlorophenol (TCP), 2,3,4,6-tetrachlorophenol (TeCP), 2,4,6-tribromophenol (TBP) and pentachlorophenol (PCP) from wine. The haloanisoles and halophenols were automatically determined using a
Kristina Arnoldsson et al.
Environmental science & technology, 46(13), 7239-7244 (2012-06-13)
Polybrominated dibenzo-p-dioxins (PBDD) are emerging environmental pollutants with structural similarities to the highly characterized toxicants polychlorinated dibenzo-p-dioxins. The geographical and temporal variations of PBDD in biota samples from the Baltic Sea do not display features that are normally related to
Anna Norman Haldén et al.
Aquatic toxicology (Amsterdam, Netherlands), 100(1), 30-37 (2010-08-20)
The bromophenol 2,4,6-tribromophenol (TBP) is widely used as an industrial chemical, formed by degradation of tetrabromobisphenol-A, and it occurs naturally in marine organisms. Concentrations of TBP in fish have been related to intake via feed, but little is known about
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