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F3800

Sigma-Aldrich

4-Fluoroaniline

99%

Sinônimo(s):

1-Amino-4-fluorobenzene

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About This Item

Fórmula linear:
FC6H4NH2
Número CAS:
371-40-4
Peso molecular:
111.12
Beilstein:
742030
Número CE:
206-735-5
Número MDL:
MFCD00007829
Código UNSPSC:
12352100
ID de substância PubChem:
24894858
NACRES:
NA.22

Ensaio

99%

forma

liquid

índice de refração

n20/D 1.539 (lit.)

pb

187 °C/767 mmHg (lit.)

densidade

1.173 g/mL at 25 °C (lit.)

cadeia de caracteres SMILES

Nc1ccc(F)cc1

InChI

1S/C6H6FN/c7-5-1-3-6(8)4-2-5/h1-4H,8H2

chave InChI

KRZCOLNOCZKSDF-UHFFFAOYSA-N

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Categorias relacionadas

Palavra indicadora

Danger

Frases de perigo

H302,H314,H373,H410

Classificações de perigo

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Dam. 1 - Skin Corr. 1C - STOT RE 2

Órgãos-alvo

Blood,hematopoietic system

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 1

Ponto de fulgor (°F)

162.9 °F

Ponto de fulgor (°C)

72.7 °C

Equipamento de proteção individual

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

Certificados de análise (COA)

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Sigma-Aldrich

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4-Fluoro-N-methylaniline

2,4,6-Trifluoroaniline ≥97%

Sigma-Aldrich

196835

2,4,6-Trifluoroaniline

p-Toluidine 99.6%

Sigma-Aldrich

236314

p-Toluidine

C V Eadsforth et al.
Xenobiotica; the fate of foreign compounds in biological systems, 16(6), 555-566 (1986-06-01)
o-Fluoroaniline is rapidly metabolized and excreted in rats, rabbits and marmosets. Following a single oral dose of 14C-fluoroaniline of about 20 mg/kg, more than 80% of the dose is excreted in 0-24 h, the urine being the major route of
Meizhen Wang et al.
Environmental science and pollution research international, 20(9), 6201-6209 (2013-04-17)
To develop a bacterial bioaugmentation system for fluorine-containing industrial wastewater treatment, optimal conditions for 4-fluoroaniline (4-FA) degradation and autoinducer release in Acinetobacter sp. TW were determined. Quorum sensing in biofilms of strain TW was also investigated. Different optimal conditions exist
G B Scarfe et al.
Xenobiotica; the fate of foreign compounds in biological systems, 29(2), 205-216 (1999-04-13)
1. The urinary metabolic fate of 4-fluoroaniline (4-FA) and 1-[13C]-4-fluoroacetanilide (4-FAA) has been studied using NMR-based methods after 50 and 100 mg kg(-1) i.p. doses respectively to the male Sprague-Dawley rat. 2. 4-FA was both ortho- and para-hydroxylated. The major
I M Rietjens et al.
Chemico-biological interactions, 77(3), 263-281 (1991-01-01)
Metabolism and bioactivation of fluoroanilines was studied both in vitro in microsomal systems and in vivo. 4-Fluoroaniline and pentafluoroaniline and their non-para fluorinated analogues were used as the model compounds. Special attention was focussed on bioactivation to reactive benzoquinoneimines. Cytochrome
J G Bundy et al.
Xenobiotica; the fate of foreign compounds in biological systems, 32(6), 479-490 (2002-08-06)
1. Little is known about metabolism of xenobiotics by earthworms, despite their importance in soil ecotoxicity testing. Normal earthworms and earthworms treated with antibiotics to ensure inhibition of gut microflora were exposed to two model xenobiotic compounds, 4-fluoroaniline and 4-fluorobiphenyl
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