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Supelco

2,4,6-Tribromophenol

analytical standard

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About This Item

Linear Formula:
Br3C6H2OH
CAS Number:
118-79-6
Molecular Weight:
330.80
Beilstein:
776920
EC Number:
204-278-6
MDL number:
MFCD00002150
UNSPSC Code:
41116107
PubChem Substance ID:
329755537

grade

analytical standard

vapor density

11.4 (vs air)

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

bp

282-290 °C/746 mmHg (lit.)

mp

90-94 °C (lit.)

application(s)

environmental

format

neat

SMILES string

Oc1c(Br)cc(Br)cc1Br

InChI

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

InChI key

BSWWXRFVMJHFBN-UHFFFAOYSA-N

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Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Pictograms

Exclamation markEnvironment
GHS07,GHS09

Signal Word

Warning

Hazard Statements

H317,H319,H400

Hazard Classifications

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

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

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Certificates of Analysis (COA)

Lot/Batch Number
BCCJ9553
BCBW8501

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Hidetoshi Kuramochi et al.
Journal of environmental monitoring : JEM, 10(2), 206-210 (2008-02-05)
2,4,6-Tribromophenol (TBP) is expected to exist in both ionic and non-ionic forms in the environment due to ionisation of the phenolic group at near neutral pH. In this study, the water solubility (Sw) and 1-octanol-water partition coefficient (Kow) of aqueous
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
Lei Zu et al.
Bioresource technology, 110, 153-159 (2012-02-24)
A strain Bacillus sp. GZT capable of debrominating and mineralizing 2,4,6-tribromophenol (TBP) was isolated and characterized by morphological observation, biochemical and physiological identification as well as 16S rRNA sequence analysis. Biodegradation kinetics experiments demonstrated that initial TBP concentration had a
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
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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