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16230

Sigma-Aldrich

4-Bromoaniline

≥99.0% (GC)

Sinônimo(s):

1-Amino-4-bromobenzene, p-Bromoaniline

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About This Item

Fórmula linear:
BrC6H4NH2
Número CAS:
Peso molecular:
172.02
Beilstein:
742031
Número CE:
Número MDL:
Código UNSPSC:
12352100
ID de substância PubChem:
NACRES:
NA.22

Ensaio

≥99.0% (GC)

forma

solid

pf

56-62 °C (lit.)
63-65 °C

solubilidade

ethanol: soluble 0.5 g/10 mL, clear, colorless to almost colorless

cadeia de caracteres SMILES

Nc1ccc(Br)cc1

InChI

1S/C6H6BrN/c7-5-1-3-6(8)4-2-5/h1-4H,8H2

chave InChI

WDFQBORIUYODSI-UHFFFAOYSA-N

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Descrição geral

Photocatalytic degradation of 4-bromoaniline over ZnO or TiO2 (anatase and rutile) has been investigated in a photocatalytic reactor.

Aplicação

4-Bromoaniline was used as carbon and nitrogen supplement in the culture medium of Moraxella sp. strain G.

Ações bioquímicas/fisiológicas

4-Bromoaniline reduces gluconeogenesis in renal cortical slices obtained from the kidneys of untreated, male Fischer 344 rats.

Palavra indicadora

Danger

Classificações de perigo

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - STOT RE 2

Código de classe de armazenamento

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Equipamento de proteção individual

dust mask type N95 (US), Eyeshields, Faceshields, Gloves


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Mohammad Hossein Habibi et al.
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Photocatalytic degradation of aqueous solution of aniline derivatives such as ortho-nitroaniline (ONA), meta-nitroaniline (MNA), para-nitroaniline (PNA), 4-bromoaniline (4-BrA) and 2-chloroaniline (2-ClA) were carried out over ZnO or TiO2 (anatase and rutile) in a photocatalytic reactor. The observed results revealed that
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PloS one, 15(11), e0241849-e0241849 (2020-11-20)
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Toxicology letters, 114(1-3), 125-133 (2000-03-14)
Haloanilines are widely used as chemical intermediates in the manufacture of pesticides, dyes and drugs. The purpose of this study was to examine the in vitro nephrotoxic effects of the four 4-haloaniline and four 3,5-dihaloaniline isomers using renal cortical slices
H Major et al.
Xenobiotica; the fate of foreign compounds in biological systems, 33(8), 855-869 (2003-08-26)
1. The metabolic fate of 4-bromoaniline (4-BrA) was investigated in rat following intraperitoneal administration at 50 mg kg(-1) using HPLC-TOF-MS/MS. 2. The sensitivity provided by the use of TOF-MS/MS, aided by the distinctive isotope pattern resulting from the presence of
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