F3401
2-氟苯胺
≥99%
别名:
1-氨基-2-氟苯
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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
UNSPSC Code:
12352116
NACRES:
NA.25
PubChem Substance ID:
EC Number:
206-478-9
Beilstein/REAXYS Number:
1524219
MDL number:
产品名称
2-氟苯胺, ≥99%
InChI
1S/C6H6FN/c7-5-3-1-2-4-6(5)8/h1-4H,8H2
InChI key
FTZQXOJYPFINKJ-UHFFFAOYSA-N
SMILES string
Nc1ccccc1F
assay
≥99%
refractive index
n20/D 1.544 (lit.)
bp
182-183 °C (lit.)
mp
−29 °C (lit.)
density
1.151 g/mL at 25 °C (lit.)
Quality Level
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Biochem/physiol Actions
由于人体暴露在制造中，异生素化合物 2-氟苯胺的代谢和排泄是重要的。发现它非常有效地代谢，主要是通过 4-羟基化，随后形成硫酸盐或葡糖苷酸。还观察到 N-乙酰化。至少 80％ 的剂量在 24 小时内从尿液中排出。2-氟苯胺通过 4-羟基化和随后的对苯醌亚胺形成发挥其肾毒性作用。
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Dam. 1 - Flam. Liq. 3 - Skin Corr. 1C - STOT RE 2
target_organs
Blood,hematopoietic system
存储类别
3 - Flammable liquids
wgk
WGK 2
flash_point_f
140.0 °F - closed cup
flash_point_c
60 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
法规信息
危险化学品
此项目有
M Arivazhagan et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 96, 668-676 (2012-08-14)
The Fourier transform infrared (FT-IR) and Fourier transform Raman (FT-Raman) spectra of 4-chloro-2-fluoroaniline (CFA) have been recorded and analyzed. The equilibrium geometry, bonding features and harmonic vibrational frequencies have been investigated with the help of ab initio and density functional
A L Sharma et al.
Applied biochemistry and biotechnology, 96(1-3), 155-165 (2002-01-11)
Poly(2-fluoroaniline) was prepared by both chemical and electrochemical polymerization in acidic medium. Characterization of poly(2-fluoroaniline) was accomplished experimentally using ultraviolet-visible, Fourier transform infrared, differential scanning calorimetry, thermal gravimetric analysis, and X-ray diffraction techniques, respectively. Scanning electron microscopy studies revealed globular
M A Valentovic et al.
Toxicology, 75(2), 121-131 (1992-11-01)
Aniline and its halogenated derivatives are widely used as chemical intermediates. The purpose of this study was to determine the hepatotoxic and nephrotoxic potential of the 2-haloanilines. Male Fischer 344 rats (n > or = 4) were injected (i.p.) with
J Vervoort et al.
NMR in biomedicine, 4(6), 255-261 (1991-12-01)
The present study describes results from an in vivo 19F NMR study on rats exposed to the xenobiotic compound 2-fluoroaniline. Qualitative pharmacokinetics and the biotransformation of 2-fluoroaniline were studied after exposure to 50 mg/kg body wt 2-fluoroaniline. Accumulation and elimination
Suria Jahan et al.
Transfusion, 60(4), 769-778 (2020-03-19)
Platelet engraftment following cord blood (CB) transplantation remains a significant hurdle to this day. The uncontrolled growth of ice, a process referred to as ice recrystallization, is one of several mechanisms that lead to cell loss and decreased potency during
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