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线性分子式:
FC6H4NH2
化学文摘社编号:
分子量:
111.12
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
206-735-5
Beilstein/REAXYS Number:
742030
MDL number:
Assay:
99%
Form:
liquid
InChI key
KRZCOLNOCZKSDF-UHFFFAOYSA-N
InChI
1S/C6H6FN/c7-5-1-3-6(8)4-2-5/h1-4H,8H2
SMILES string
Nc1ccc(F)cc1
assay
99%
form
liquid
bp
187 °C/767 mmHg (lit.)
density
1.173 g/mL at 25 °C (lit.)
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
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
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
Rex Patrick et al.
Journal of pharmaceutical and biomedical analysis, 56(4), 721-727 (2011-08-16)
Collision-induced dissociation (CID) mass spectra of a few haloaniline isomers, (chloroanilines, dichloroanilines, difluoroanilines, chloro-fluoroanilines and bromo-fluoroanilines) were characterized. The mass spectral behaviour of difluoroanilines was different from those of the corresponding regioisomers of the other haloanilines. For all ortho regioisomers
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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