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F3800

Sigma-Aldrich

4-Fluoroaniline

99%

Sinonimo/i:

1-Amino-4-fluorobenzene

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About This Item

Formula condensata:
FC6H4NH2
Numero CAS:
371-40-4
Peso molecolare:
111.12
Beilstein:
742030
Numero CE:
206-735-5
Numero MDL:
MFCD00007829
Codice UNSPSC:
12352100
ID PubChem:
24894858
NACRES:
NA.22

Saggio

99%

Stato

liquid

Indice di rifrazione

n20/D 1.539 (lit.)

P. ebollizione

187 °C/767 mmHg (lit.)

Densità

1.173 g/mL at 25 °C (lit.)

Stringa SMILE

Nc1ccc(F)cc1

InChI

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

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Avvertenze

Danger

Indicazioni di pericolo

H302,H314,H373,H410

Classi di pericolo

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

Organi bersaglio

Blood,hematopoietic system

Codice della classe di stoccaggio

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

Classe di pericolosità dell'acqua (WGK)

WGK 1

Punto d’infiammabilità (°F)

162.9 °F

Punto d’infiammabilità (°C)

72.7 °C

Dispositivi di protezione individuale

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

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Certificati d'analisi (COA)

Lot/Batch Number
MKCL9467
MKCL1920
WXBC7912V
WXBC2194V
WXBB7908V

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4-Fluoro-N-methylaniline 97%

Sigma-Aldrich

223069

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

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
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
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
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
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
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