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Key Documents

229237

Sigma-Aldrich

4,4′-Dibromobiphenyl

98%

Sinônimo(s):

1-Bromo-4-(4-bromophenyl)benzene, 4,4′-Dibromo-1,1′-biphenyl, 4,4′-Dibromodiphenyl, 4′,4-Dibromobiphenyl, PBB 15, p,p′-Dibromobiphenyl

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About This Item

Fórmula linear:
BrC6H4C6H4Br
Número CAS:
Peso molecular:
312.00
Beilstein:
2044701
Número CE:
Número MDL:
Código UNSPSC:
12352100
ID de substância PubChem:
NACRES:
NA.22

Nível de qualidade

Ensaio

98%

forma

solid

pb

355-360 °C (lit.)

pf

163-165 °C (lit.)

cadeia de caracteres SMILES

Brc1ccc(cc1)-c2ccc(Br)cc2

InChI

1S/C12H8Br2/c13-11-5-1-9(2-6-11)10-3-7-12(14)8-4-10/h1-8H

chave InChI

HQJQYILBCQPYBI-UHFFFAOYSA-N

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Descrição geral

The degradation of 4,4′-dibromobiphenyl, through photoelectrocatalytic process, was studied.

Palavra indicadora

Danger

Classificações de perigo

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

Órgãos-alvo

Respiratory system

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 1

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Equipamento de proteção individual

Eyeshields, Gloves, type N95 (US)


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Marola M H van Lipzig et al.
Chemical research in toxicology, 18(11), 1691-1700 (2005-11-23)
Exposure of humans and wildlife to xenobiotics, such as halogenated biphenyls, that interfere with the endogenous estrogen balance may lead to endocrine disruption. Such compounds may either mimic or block estradiol's action by agonistic or antagonistic action, respectively. They may
Jinyang Chen et al.
Journal of hazardous materials, 235-236, 85-91 (2012-07-31)
In situ transformation of 4,4'-Dibromobiphenyl (4,4'-DBB) in water was observed with hydrothermal diamond anvil cell (HDAC) up to 633 K. It shows that 4,4'-DBB dissolves in water to form a homogenous phase at the temperature of 588 K and thus
Sierra Rayne et al.
Water research, 37(3), 551-560 (2003-04-12)
The anaerobic microbial and photochemical degradation pathways of 4,4'-dibromodiphenyl ether (BDE15) were examined. BDE15 was reductively debrominated within a fixed-film plug-flow biological reactor at hydraulic retention times of 3.4 and 6.8 h, leading to exclusive production of 4-bromodiphenyl ether (BDE3)
Haijin Liu et al.
Chemosphere, 82(1), 43-47 (2010-11-03)
Polybrominated biphenyls have been widely used as flameretardants in textile and electronic industries, and additives in plastics. Over the past few decades, much attention has been given to polybrominated biphenyls in the environment and their effects on humans. In this
Shanshan Qiu et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 76(5), 429-434 (2010-05-11)
In this work, both experimental and theoretical study on the FT-IR and Raman spectra as well as (1)H NMR and (13)C NMR chemical shifts of 4,4'-dibromodiphenyl ether have been carried out. The optimized geometry was obtained by using both HF

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