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35829

Supelco

2,4-Dichloroaniline

PESTANAL®, analytical standard

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About This Item

Linear Formula:
Cl2C6H3NH2
CAS Number:
Molecular Weight:
162.02
Beilstein:
386422
EC Number:
MDL number:
UNSPSC Code:
41116107
eCl@ss:
39050667
PubChem Substance ID:
NACRES:
NA.24

grade

analytical standard

Quality Level

product line

PESTANAL®

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

bp

245 °C (lit.)

mp

59-62 °C (lit.)

application(s)

agriculture
environmental

format

neat

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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Application

2,4-Dichloroaniline may be used as an analytical reference standard for the determination of the analyte in water samples by ultrasound-assisted ionic liquid dispersive liquid-phase micro-extraction, capillary electrophoresis with electrochemical and fluorescence detection and gas chromatography-mass spectrometry (GC-MS), respectively.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

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Legal Information

PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany

Pictograms

Skull and crossbonesEnvironment

Signal Word

Danger

Hazard Statements

Hazard Classifications

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

Storage Class Code

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

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

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Ultrasound-assisted ionic liquid dispersive liquid-phase micro-extraction: A novel approach for the sensitive determination of aromatic amines in water samples.
Zhou Q, et al.
Journal of Chromatography A, 1216(20), 4361-4365 (2009)
Determination of aromatic amines in water samples by capillary electrophoresis with electrochemical and fluorescence detection.
Asthana A, et al.
Journal of Chromatography A, 895(1-2), 197-203 (2000)
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
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

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