D101400
2,4-Difluoroaniline
99%
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About This Item
Linear Formula:
F2C6H3NH2
CAS Number:
Molecular Weight:
129.11
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
206-687-5
Beilstein/REAXYS Number:
2802556
MDL number:
Assay:
99%
Form:
liquid
InChI key
CEPCPXLLFXPZGW-UHFFFAOYSA-N
InChI
1S/C6H5F2N/c7-4-1-2-6(9)5(8)3-4/h1-3H,9H2
SMILES string
Nc1ccc(F)cc1F
assay
99%
form
liquid
Quality Level
bp
170 °C/753 mmHg (lit.)
mp
−7.5 °C (lit.)
density
1.268 g/mL at 25 °C (lit.)
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 3 Dermal - Acute Tox. 4 Oral
Storage Class
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
wgk
WGK 1
flash_point_f
143.6 °F - closed cup
flash_point_c
62 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
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Wei Chih Huang et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 93, 176-179 (2012-04-07)
We applied the two-color resonant two-photon ionization and mass-analyzed threshold ionization techniques to record the vibronic and cation spectra of 2,4-difluoroaniline. The cation spectra were recorded by ionizing via the 0(0), X(1), 6b(1), and 1(1) levels of the electronically excited
Duoli Guo et al.
AAPS PharmSciTech, 13(2), 661-673 (2012-05-04)
A stability-indicating high-performance liquid chromatography method to quantify 2-(2,4-difluorophenyl)-4,5,6,7-tetrafluoroisoindoline-1,3-dione (NSC-726796) and its three main degradation products was developed. This method was used to investigate its degradation kinetics and mechanism. The reaction follows first-order kinetics and appears to be base catalyzed
P J Boogaard et al.
Environmental health perspectives, 102 Suppl 6, 27-29 (1994-10-01)
Exposure to 2,4-difluoroaniline (DFA) was monitored by GC-MS of DFA adducts bound to hemoglobin (Hb). In two studies, involving 20 and 16 workers potentially exposed to low concentrations of DFA, median concentrations of 10 (range 1-83) and 20 (range 4-322)
Sergey E Korchak et al.
The Journal of chemical physics, 137(9), 094503-094503 (2012-09-11)
Effects of spin-spin interactions on the nuclear magnetic relaxation dispersion (NMRD) of protons were studied in a situation where spin ½ hetero-nuclei are present in the molecule. As in earlier works [K. L. Ivanov, A. V. Yurkovskaya, and H.-M. Vieth
Junyu Guo et al.
Environmental pollution (Barking, Essex : 1987), 225, 175-183 (2017-04-04)
Trifluoroacetic acid (TFA) in the atmosphere is produced by degradation of hydrochlorofluorocarbons and hydrofluorocarbons. In recent years, TFA has attracted global attention because of increased environmental concentrations, biological toxicity and accumulation in aqueous environments. This study focused on the mechanisms
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