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35170

Sigma-Aldrich

2,4-Dichloroaniline

≥97.0% (GC)

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About This Item

Linear Formula:
Cl2C6H3NH2
CAS Number:
554-00-7
Molecular Weight:
162.02
Beilstein/REAXYS Number:
386422
EC Number:
209-057-8
MDL number:
MFCD00007661
UNSPSC Code:
12352100
PubChem Substance ID:
57649345
NACRES:
NA.22

assay

≥97.0% (GC)

bp

245 °C (lit.)

mp

59-62 °C (lit.)
60-65 °C

solubility

methanol: soluble, clear, very faintly brownish-yellow

SMILES string

Nc1ccc(Cl)cc1Cl

InChI

1S/C6H5Cl2N/c7-4-1-2-6(9)5(8)3-4/h1-3H,9H2

InChI key

KQCMTOWTPBNWDB-UHFFFAOYSA-N

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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.

pictograms

Skull and crossbonesEnvironment
GHS06,GHS09

signalword

Danger

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 4 Oral - Aquatic Chronic 2

Storage Class

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

wgk_germany

WGK 3

flash_point_f

239.0 °F - closed cup

flash_point_c

115 °C - closed cup

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Certificates of Analysis (COA)

Lot/Batch Number
BCCC5333
BCCC3188
WXBC4269V
WXBC1564V
WXBC1564V

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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)
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
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
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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