46490
4-氟苯胺
technical, ≥97.0% (GC)
别名:
对氟苯胺
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关于此项目
线性分子式:
FC6H4NH2
化学文摘社编号:
分子量:
111.12
EC Number:
206-735-5
UNSPSC Code:
12352100
PubChem Substance ID:
Beilstein/REAXYS Number:
742030
MDL number:
grade
technical
assay
≥97.0% (GC)
refractive index
n20/D 1.539 (lit.), n20/D 1.540
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
General description
The barriers to inversion and internal rotation of the NH2 group in 4-fluoroaniline has been investigated by far infrared gas spectra.
Application
4-Fluoroaniline may be employed as one of the target pollutant during the investigation of biodegradability of fluorinated compounds under aerobic conditions. It may be used for the synthesis of luminescent and cationic monocyclometalated gold(III) monoaryl complexes.
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Dam. 1 - Skin Corr. 1C - STOT RE 2
target_organs
Blood,hematopoietic system
存储类别
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
wgk
WGK 1
flash_point_f
162.9 °F
flash_point_c
72.7 °C
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
法规信息
危险化学品
此项目有
Far infrared investigation of aniline and 4-fluoroaniline in the vapour phase. Inversion and torsion of the amino group.
Larsen NW, et al.
Chemical Physics Letters, 43(3), 584-586 (1976)
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
Zhi-Qing Zhao et al.
Biodegradation, 26(1), 1-14 (2014-09-23)
The fate of fluorinated compounds in the environment, especially polyfluorinated aromatics, is a matter of great concern. In this work, 4-Fluoroaniline (4-FA), 2,4-Difluoroanilines (2,4-DFA), and 2,3,4-Trifluoroanilines (2,3,4-TFA), were chosen as the target pollutants to study their biodegradability under aerobic conditions.
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
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