Skip to Content
Merck
CN
All Photos(3)

Documents

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

Sign Into View Organizational & Contract Pricing
All Photos(3)

About This Item

Linear Formula:
Cl2C6H3NH2
CAS Number:
95-76-1
Molecular Weight:
162.02
Beilstein:
636837
EC Number:
202-448-4
MDL number:
MFCD00007768
UNSPSC Code:
12352100
PubChem Substance ID:
24867396
NACRES:
NA.22

Quality Level

100

Assay

98%

bp

272 °C (lit.)

mp

69-71 °C (lit.)

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

Looking for similar products? Visit Product Comparison Guide

Related Categories

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

WGK

WGK 3

Flash Point(F)

275.0 °F

Flash Point(C)

135.00 °C

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

危险化学品

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

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
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
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).
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
View All Related Papers

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service