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Key Documents

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D101400

Sigma-Aldrich

2,4-Difluoroaniline

99%

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About This Item

Fórmula lineal:
F2C6H3NH2
Número de CAS:
367-25-9
Peso molecular:
129.11
Beilstein/REAXYS Number:
2802556
EC Number:
206-687-5
MDL number:
MFCD00007648
UNSPSC Code:
12352100
PubChem Substance ID:
24893321
NACRES:
NA.22

assay

99%

form

liquid

refractive index

n20/D 1.506 (lit.)

bp

170 °C/753 mmHg (lit.)

mp

−7.5 °C (lit.)

density

1.268 g/mL at 25 °C (lit.)

SMILES string

Nc1ccc(F)cc1F

InChI

1S/C6H5F2N/c7-4-1-2-6(9)5(8)3-4/h1-3H,9H2

InChI key

CEPCPXLLFXPZGW-UHFFFAOYSA-N

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pictograms

Skull and crossbones
GHS06

signalword

Danger

hcodes

H302,H311

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_germany

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

Certificados de análisis (COA)

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Sigma-Aldrich

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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
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
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
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)
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
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