All Photos(3)
Synonym(s):
2,4-Dichlorophenylamine, 4-Chloro-2-chloroaniline
Linear Formula:
Cl2C6H3NH2
CAS Number:
Molecular Weight:
162.02
Beilstein:
386422
EC Number:
MDL number:
UNSPSC Code:
12352100
eCl@ss:
39050667
PubChem Substance ID:
NACRES:
NA.22
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Quality Level
Assay
99%
form
solid
bp
245 °C (lit.)
mp
59-62 °C (lit.)
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 degraded by Delftia tsuruhatensis H1. 2,4-Dichloroaniline metabolite is detected in human urine sample by GC/MS and high performance liquid chromatograph.
Application
- Phototransformation of 2,4-Dichloroaniline: Studies the phototransformation of 2,4-Dichloroaniline in freshwater environments, crucial for understanding its environmental degradation and implications for water purification technologies (Ucun et al., 2021).
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 4 Oral - Aquatic Chronic 2
WGK
WGK 3
Flash Point(F)
closed cup
Flash Point(C)
closed cup
Regulatory Information
危险化学品
Certificates of Analysis (COA)
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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
I Leguen et al.
Aquatic toxicology (Amsterdam, Netherlands), 53(3-4), 201-214 (2001-06-16)
Their functions and localisation can expose gill cells to volume changes. To maintain their vital functions, these gill cells must regulate their own volume after cellular swelling or shrinkage. Recently, we showed that rainbow trout pavement gill cells in primary
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
Sophie Pascal-Lorber et al.
Journal of agricultural and food chemistry, 51(16), 4712-4718 (2004-01-07)
The uptake and metabolism of [14C]-2,4-dichlorophenol (DCP) and [14C]-2,4-dichloroaniline (DCA) were investigated in wheat and soybean. Seeds were exposed to a nutrient solution containing 50 microM of one of two radiolabeled compounds, and plant organs were harvested separately after 18
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