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Merck

258164

Sigma-Aldrich

2,4-Dibromphenol

95%

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About This Item

Lineare Formel:
Br2C6H3OH
CAS-Nummer:
Molekulargewicht:
251.90
Beilstein:
1861291
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
12352100
PubChem Substanz-ID:
NACRES:
NA.22

Assay

95%

Form

solid

bp

154 °C/11 mmHg (lit.)

mp (Schmelzpunkt)

35-38 °C (lit.)

SMILES String

Oc1ccc(Br)cc1Br

InChI

1S/C6H4Br2O/c7-4-1-2-6(9)5(8)3-4/h1-3,9H

InChIKey

FAXWFCTVSHEODL-UHFFFAOYSA-N

Angaben zum Gen

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Allgemeine Beschreibung

The electrochemical hydrodehalogenation of 2,4-dibromophenol has been studied by electrochemical reduction in H-cells and solid polymer electrolyte cells using catalyzed cathodes. 2,4-Dibromophenol inhibits the microbial activity in marine sediments.

Piktogramme

Skull and crossbones

Signalwort

Danger

Gefahreneinstufungen

Acute Tox. 2 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Zielorgane

Respiratory system

Lagerklassenschlüssel

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

WGK

WGK 3

Flammpunkt (°F)

235.4 °F - closed cup

Flammpunkt (°C)

113 °C - closed cup

Persönliche Schutzausrüstung

Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges


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Inhibition of microbial activity in marine sediments by a bromophenol from a hemichordate.
King GM.
Nature, 323(6085), 257-259 (1986)
H Cheng et al.
Environmental science & technology, 38(2), 638-642 (2004-01-31)
A new technology for remediation of halogenated organics-oil systems, which can cause serious environmental problems, has been demonstrated using the electrochemical hydrodehalogenation of 2,4-dibromophenol (DBP) in paraffin oil in a solid polymer electrolyte reactor. The reactor has been evaluated in
G M King
Applied and environmental microbiology, 54(12), 3079-3085 (1988-12-01)
Halophenols such as 2,4-dibromophenol (DBP) occur naturally in some marine sediments, as a consequence of various animal and algal activities. In an earlier study, DBP was observed in the burrow microenvironment of the hemichordate Saccoglossus kowalewskii. At the concentrations found
Hui Liu et al.
Chemosphere, 84(4), 512-518 (2011-04-05)
Hydroxylated polybrominated diphenyl ethers (HO-PBDEs) have received significant attention due to their toxicities and universal presence in the environmental matrices. However, their origins are not fully understood. We explored the feasibility of the generation of HO-PBDEs through photochemical processes from
Keun Young Kim et al.
Journal of food science, 75(5), H145-H150 (2010-07-16)
A bromophenol, bis(2,3-dibromo-4,5-dihydroxybenzyl) ether, was purified from the red alga Polyopes lancifolia. Its IC(50) values were 0.098 and 0.120 microM against Saccharomyces cerevisiae and Bacillus stearothermophilus alpha-glucosidases, respectively, and 1.00 and 1.20 mM against rat-intestinal sucrase and maltase. This bromophenol

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