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 Level
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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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
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
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
Global Trade Item Number
| SKU | GTIN |
|---|---|
| F3401-100G-A | 04061833613863 |
| F3401-25G-A | 04061833613917 |
| F3401-500G-A | 04061837692215 |