F3401
2-Fluoroaniline
≥99%
Synonym(s):
1-Amino-2-fluorobenzene
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About This Item
Linear Formula:
FC6H4NH2
CAS Number:
Molecular Weight:
111.12
UNSPSC Code:
12352116
NACRES:
NA.25
PubChem Substance ID:
EC Number:
206-478-9
Beilstein/REAXYS Number:
1524219
MDL number:
Assay:
≥99%
Quality Segment
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.)
SMILES string
Nc1ccccc1F
InChI
1S/C6H6FN/c7-5-3-1-2-4-6(5)8/h1-4H,8H2
InChI key
FTZQXOJYPFINKJ-UHFFFAOYSA-N
Biochem/physiol Actions
The metabolism and excretion of the xenobiotic compound 2-fluoroaniline is important due to human exposure in manufacturing. It is found to be very efficiently metabolized, primarily by 4-hydroxylation with subsequent sulfate or glucuronide formation. N-Acetylation is also observed. At least 80% of the dose is excreted in the urine within 24 hr. 2-Fluoroaniline exerts its nephrotoxic effect through 4-hyroxylation and subsequent p-benzoquinonimine formation.
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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
Storage Class
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
Regulatory Information
危险化学品
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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
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 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
Global Trade Item Number
| SKU | GTIN |
|---|---|
| F3401-100G-A | 04061833613863 |
| F3401-25G-A | 04061833613917 |
| F3401-500G-A | 04061837692215 |