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MilliporeSigma

258164

2,4-Dibromophenol

95%

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$136.85

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About This Item

Linear Formula:
Br2C6H3OH
CAS Number:
615-58-7
Molecular Weight:
251.90
Beilstein/REAXYS Number:
1861291
EC Number:
210-436-5
MDL number:
MFCD00002149
UNSPSC Code:
12352100
PubChem Substance ID:
24855633
NACRES:
NA.22

Key Documents

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Quality Level

100

assay

95%

form

solid

bp

154 °C/11 mmHg (lit.)

mp

35-38 °C (lit.)

functional group

bromo

SMILES string

Oc1ccc(Br)cc1Br

InChI

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

InChI key

FAXWFCTVSHEODL-UHFFFAOYSA-N

Gene Information

human ... ALOX12(239), ALOX15(246)

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249440137715252018
2,4-Dibromophenol 95%

Sigma-Aldrich

258164

2,4-Dibromophenol

Hydrocinnamoyl chloride 98%

Sigma-Aldrich

249440

Hydrocinnamoyl chloride

2,4,6-Tribromophenol 99%

Sigma-Aldrich

137715

2,4,6-Tribromophenol

2,6-Dibromophenol 99%

Sigma-Aldrich

252018

2,6-Dibromophenol

assay

95%

assay

98%

assay

99%

assay

99%

Quality Level

100

Quality Level

100

Quality Level

100

Quality Level

100

mp

35-38 °C (lit.)

mp

−7-−5 °C (lit.)

mp

90-94 °C (lit.)

mp

53-56 °C (lit.)

bp

154 °C/11 mmHg (lit.)

bp

107 °C/11 mmHg (lit.)

bp

282-290 °C/746 mmHg (lit.)

bp

255-256 °C/740 mmHg (lit.)

form

solid

form

liquid

form

-

form

solid

functional group

bromo

functional group

acyl chloride, phenyl

functional group

bromo

functional group

bromo

General description

The electrochemical hydrodehalogenation of 2,4-dibromophenol has been studied by electrochemical reduction in H-cells and solid polymer electrolyte cells using catalyzed cathodes[1]. 2,4-Dibromophenol inhibits the microbial activity in marine sediments[2].

pictograms

Skull and crossbones
GHS06

signalword

Danger

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

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

wgk_germany

WGK 3

flash_point_f

235.4 °F - closed cup

flash_point_c

113 °C - closed cup

ppe

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

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Certificates of Analysis (COA)

Lot/Batch Number
STBL3393
STBL1684
STBK9550
STBK0490
STBJ7584

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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)
Aliaksandr I Balabanovich et al.
Environmental science & technology, 39(14), 5469-5474 (2005-08-09)
Halogen-containing aromatics, mainly bromine-containing phenols, are harmful compounds contaminating pyrolysis oil from electronic boards containing halogenated flame retardants. In addition,theirformation increases the potential for evolution of polybrominated dibenzo-p-dioxins (PBDDs) and dibenzofurans (PBDFs) at relatively low temperature (up to 500 degrees
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
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
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