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281999

Sigma-Aldrich

4-Bromobiphenyl

98%

Synonym(s):

(4-Bromophenyl)benzene, 1-Bromo-4-phenylbenzene, 4-Biphenyl bromide, 4′-Bromobiphenyl, p-Phenylphenyl bromide

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About This Item

Linear Formula:
C6H5C6H4Br
CAS Number:
92-66-0
Molecular Weight:
233.10
Beilstein:
1907453
EC Number:
202-176-6
MDL number:
MFCD00000100
UNSPSC Code:
12352100
PubChem Substance ID:
24857009
NACRES:
NA.22
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Quality Level

100

Assay

98%

form

solid

bp

310 °C (lit.)

mp

82-86 °C (lit.)

functional group

bromo
phenyl

SMILES string

Brc1ccc(cc1)-c2ccccc2

InChI

1S/C12H9Br/c13-12-8-6-11(7-9-12)10-4-2-1-3-5-10/h1-9H

InChI key

PKJBWOWQJHHAHG-UHFFFAOYSA-N

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General description

In vitro metabolism of 4-bromobiphenyl by cytochrome P-450-dependent monooxygenases in rat hepatic microsomes has been investigated[1]. 4-Bromobiphenyl undergoes reduction to biphenyl in cationic micelles (cetyltrimethyl-ammonium bromide) by electrochemically generated anion radicals of 9-phenylanthracene[2].

Application

4-Bromobiphenyl was used in the synthesis of 4-biphenylthiolate[1].

Signal Word

Danger

Hazard Statements

H302,H315,H318,H335,H400

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Acute 1 - Eye Dam. 1 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

EU REACH Annex XVII (Restriction List)

CAS No.

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Certificates of Analysis (COA)

Lot/Batch Number
STBG6919
STBD2171V
MKBK4180V
MKBH9142V
MKBF2857V

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Electrocatalytic reactions in organized assemblies: Part I. Reduction of 4-bromobiphenyl in cationic and non-ionic micelles.
Rusling JF, et al.
J. Electroanal. Chem. Interfac. Electrochem., 240(1), 201-216 (1988)
Structure of 4-biphenylthiolate on Au nanoparticle surfaces studied by UV-Vis absorption spectroscopy, transmission electron microscopy and surface-enhanced Raman scattering.
Jang S, et al.
Surface and Interface Analysis : SIA, 36(1), 43-48 (2004)
A D Davison et al.
Canadian journal of microbiology, 42(1), 66-71 (1996-01-01)
Sphingomonas paucimobilis BPSI-3 was previously isolated from a mixed microbial consortium growing on biphenyl as the sole source of carbon and energy. Transformation of 4-chlorobiphenyl (4CBP) was demonstrated by this strain, although little or no growth was observed. In minimal
A Parkinson et al.
Biochemical pharmacology, 31(10), 1849-1856 (1982-05-15)
The in vitro metabolism of biphenyl, 4-fluoro-, 4-chloro-, 4-bromo- and 4-iodobiphenyl by cytochrome P-450-dependent monooxygenases was investigated using hepatic microsomes from immature male rats pretreated with phenobarbitone or 3-methylcholanthrene. The major route of metabolism of biphenyl and the 4-halobiphenyls was
Man Wang et al.
Journal of chromatography. A, 1412, 12-21 (2015-08-19)
A new magnetic porous carbon-doped graphitic carbon nitride nanocomposite and experimental strategies were environment-friendly designed for solid phase extraction of brominated flame retardants from water sample. The easily synthesized and low cost nanocomposite was characterized using techniques, including Fourier transform

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