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F3800

Sigma-Aldrich

4-Fluoroaniline

99%

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Synonym(s):
1-Amino-4-fluorobenzene
Linear Formula:
FC6H4NH2
CAS Number:
Molecular Weight:
111.12
Beilstein/REAXYS Number:
742030
EC Number:
MDL number:
PubChem Substance ID:
NACRES:
NA.22

assay

99%

form

liquid

refractive index

n20/D 1.539 (lit.)

bp

187 °C/767 mmHg (lit.)

density

1.173 g/mL at 25 °C (lit.)

SMILES string

Nc1ccc(F)cc1

InChI

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

InChI key

KRZCOLNOCZKSDF-UHFFFAOYSA-N

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Show Differences

1 of 4

This Item
6535868.20565F8004
vibrant-m

F3800

4-Fluoroaniline

vibrant-m

653586

4-Fluoro-1,2-phenylenediamine

vibrant-m

8.20565

2-Fluoroaniline

vibrant-m

F8004

4-Fluorobenzyl chloride

density

1.173 g/mL at 25 °C (lit.)

density

-

density

1.15 g/cm3 at 20 °C

density

1.207 g/mL at 25 °C (lit.)

form

liquid

form

-

form

liquid

form

liquid

refractive index

n20/D 1.539 (lit.)

refractive index

-

refractive index

-

refractive index

n20/D 1.513 (lit.)

bp

187 °C/767 mmHg (lit.)

bp

-

bp

171-173 °C/1013 hPa

bp

82 °C/26 mmHg (lit.)

signalword

Danger

Hazard Classifications

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

Storage Class

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

wgk_germany

WGK 1

flash_point_f

162.9 °F

flash_point_c

72.7 °C

ppe

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


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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
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
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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