35170
2,4-二氯苯胺
≥97.0% (GC)
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关于此项目
线性分子式:
Cl2C6H3NH2
化学文摘社编号:
分子量:
162.02
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
209-057-8
Beilstein/REAXYS Number:
386422
MDL number:
InChI key
KQCMTOWTPBNWDB-UHFFFAOYSA-N
InChI
1S/C6H5Cl2N/c7-4-1-2-6(9)5(8)3-4/h1-3H,9H2
SMILES string
Nc1ccc(Cl)cc1Cl
assay
≥97.0% (GC)
bp
245 °C (lit.)
mp
59-62 °C (lit.), 60-65 °C
solubility
methanol: soluble, clear, very faintly brownish-yellow
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General description
2,4-Dichloroaniline is an organic xenobiotic compound and its acute toxicity, modes of action and physicochemical properties towards the freshwater crustacean amphipod Gammarus pulex has been investigated. Biodegradation of 2,4-dichloroaniline by new strain Delftia tsuruhatensis H1 has been reported. The electrochemical oxidation of 2,4-dichloroaniline was studied in acetonitrile solution. Quantitative method for the detection of 2,4-dichloroaniline in environmental water samples by solid-phase microextraction (SPME) in gas chromatography–mass spectrometry has been reported.
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 4 Oral - Aquatic Chronic 2
存储类别
6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
wgk
WGK 3
flash_point_f
239.0 °F - closed cup
flash_point_c
115 °C - closed cup
法规信息
新产品
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The electrochemical oxidation of 4-chloroaniline, 2, 4-dichloroaniline and 2, 4, 6-trichloroaniline in acetonitrile solution.
Kadar M, et al.
Electrochimica Acta, 46(9), 1297-1306 (2001)
Determination of aromatic amines by solid-phase microextraction and gas chromatography−mass spectrometry in water samples.
Muller L, et al.
Journal of Chromatography A, 791(1), 221-230 (1997)
Michael Kilemade et al.
Aquatic toxicology (Amsterdam, Netherlands), 60(1-2), 43-59 (2002-09-03)
Little or no work has been carried out on primary cell cultures in terms of cellular proliferation and toxicity studies. Cell proliferation represents one of the most relevant cellular functions. Anti-PCNA antibodies have aroused considerable interest recently as potential immunocytochemical
J Struijs et al.
Applied and environmental microbiology, 55(10), 2527-2531 (1989-10-01)
We investigated the transformation of 2,4-dichloroaniline (2,4-DiCA) and 3,4-DiCA to monochloroanilines (CA) in anaerobic pond sediment. Dechlorination of 3,4-DiCA to 3-CA started after a lag period of 3 weeks and was complete after an additional 5 weeks. Although 2,4-DiCA disappeared
N Sundaraganesan et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 73(1), 11-19 (2009-03-03)
In this work, the experimental and theoretical study on molecular structure and vibrational spectra of 2,4-dichloroaniline (2,4-DCA) were studied. The Fourier transform infrared (gas phase) and Fourier transform Raman spectra of 2,4-DCA were recorded. The molecular geometry and vibrational frequencies
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