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Safety Information

437778

Sigma-Aldrich

3,4-Dichloroaniline

98%

Synonym(s):

3,4-Dichlorobenzenamine, 3,4-Dichlorophenylamine, 4,5-Dichloroaniline, 4-Amino-1,2-dichlorobenzene, m,p-Dichloroaniline

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About This Item

Linear Formula:
Cl2C6H3NH2
CAS Number:
Molecular Weight:
162.02
Beilstein:
636837
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

98%

bp

272 °C (lit.)

mp

69-71 °C (lit.)

functional group

chloro

SMILES string

Nc1ccc(Cl)c(Cl)c1

InChI

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

InChI key

SDYWXFYBZPNOFX-UHFFFAOYSA-N

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General description

3,4-Dichloroaniline (3,4-DCA) is an aromatic amine and is a model environmental contaminant. It is an important precursor for the synthesis and degradation product of several herbicides. It is a metabolite of commonly applied herbicide, 3,4-dichloropropionanilide or propanil. Biodegradation kinetics of 3,4-DCA has been reported. Mechanism of degradation of aqueous 3,4-DCA in a novel dielectric barrier discharge plasma reactor has been studied. 1,2-dichlorobenzene, 2-chloro-1,4-benzoquinone, 3,4-dichlorophenyl isocyanate, 2-chlorohydroquinone, 3,4-dichloronitrobenzene and 3,4-dichlorophenol were identified as degradation intermediates by GC-MS analysis.

Application

3,4-Dichloroaniline may be employed as derivatization reagent for the HPLC analysis of perfluorooctanoic acid (PFOA).

Signal Word

Danger

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Dam. 1 - Skin Sens. 1

Storage Class Code

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

WGK

WGK 3

Flash Point(F)

275.0 °F - closed cup

Flash Point(C)

135.00 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

PRTR

Class I Designated Chemical Substances

ISHL Indicated Name

Substances Subject to be Indicated Names

ISHL Notified Names

Substances Subject to be Notified Names

JAN Code

437778-BULK:
437778-1KG:
437778-250G:
437778-VAR:
437778-5G:


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Guoqiang Shan et al.
Se pu = Chinese journal of chromatography, 32(9), 942-947 (2015-03-11)
A simple derivatization method followed by high performance liquid chromatography (HPLC) for the analysis of perfluorooctanoic acid (PFOA) was developed. PFOA was firstly derivatized with 3,4-dichloroaniline (DCA) using carbodiimide method. The typical amidate product was characterized by mass spectrometry (MS).
Ricardo Marques et al.
Environmental science and pollution research international, 22(9), 6687-6695 (2014-11-26)
This study models the biodegradation kinetics of two toxic xenobiotic compounds in enriched mixed cultures: a commonly applied herbicide (3,4-dichloropropionanilide or propanil) and its metabolite (3,4-dichloroaniline or DCA). The dependence of the metabolite degradation kinetics on the presence of the
M Monteiro et al.
Chemosphere, 62(8), 1333-1339 (2005-09-20)
The aromatic amine 3,4-dichloroaniline (DCA) is a model environmental contaminant, precursor for synthesis and degradation product of several herbicides, which is commonly found in European estuarine ecosystems. In this work, the possibility of using biochemical and histological markers to assess
Jingwei Feng et al.
Environmental science and pollution research international, 22(6), 4447-4459 (2014-10-16)
Degradation of aqueous 3,4-dichloroaniline (3,4-DCA) was conducted in a novel dielectric barrier discharge (DBD) plasma reactor. The factors affecting the degradation efficiency of 3,4-DCA and the degradation mechanism of 3,4-DCA were investigated. The experimental results indicated that the degradation efficiency
Nan Ye et al.
Nanotoxicology, 12(5), 423-438 (2018-04-17)
Concomitant releases of various engineered nanoparticles (NPs) into the environment have resulted in concerns regarding their combined toxicity to aquatic organisms. It is however, still elusive to distinguish the contribution to toxicity of components in NP mixtures. In the present

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