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Sigma-Aldrich

2-Chloroaniline

≥99.5% (GC)

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About This Item

Linear Formula:
ClC6H4NH2
CAS Number:
Molecular Weight:
127.57
Beilstein:
606077
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

≥99.5% (GC)

form

liquid

refractive index

n20/D 1.589

bp

208-210 °C (lit.)

mp

0-3 °C

solubility

water: soluble 5.13 g/L at 20 °C

density

1.213 g/mL at 25 °C (lit.)

SMILES string

Nc1ccccc1Cl

InChI

1S/C6H6ClN/c7-5-3-1-2-4-6(5)8/h1-4H,8H2

InChI key

AKCRQHGQIJBRMN-UHFFFAOYSA-N

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General description

2-Chloroaniline is widely used in polymer, rubber, pharmaceutical and dye industries. Determination of 2-chloroaniline in polymer industrial wastewater has been examined using HPLC with on-line microdialysis. Degradation of 2-chloroaniline in water by ozonation as well as by photolysis (UV-light of 254 nm) and radiolysis (γ-rays) in the presence of ozone has been investigated.

Signal Word

Danger

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Irrit. 2 - Muta. 2 - STOT RE 2

Storage Class Code

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

WGK

WGK 3

Flash Point(F)

221.0 °F - closed cup

Flash Point(C)

105 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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’.

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Shamsunnahar Suchana et al.
Journal of chromatography. A, 1621, 461083-461083 (2020-04-23)
A rapid and sensitive direct immersion solid-phase microextraction (SPME) technique for the analysis of seven chloro (Cl-) and nitro (NO2-) substituted anilines, toluenes, and nitrobenzenes from small volume (1.5 mL) aqueous samples was optimized for gas chromatography using Design of Experiments
Comparative studies on the degradation of aqueous 2-chloroaniline by O3 as well as by UV-light and ?-rays in the presence of ozone.
Winarno EK and Getoff N.
Radiation Physics and Chemistry, 65(4), 387-395 (2002)
H Kataoka
Journal of chromatography. A, 733(1-2), 19-34 (1996-05-10)
The environmental analysis of amines is important to preserve human health because these compounds often have toxic effects. Gas chromatography (GC) of free amines is generally unsatisfactory owing to the adsorption and decomposition of the solutes on the column. Derivatization
L Zampori et al.
Journal of hazardous materials, 170(2-3), 1041-1049 (2009-06-16)
The aim of the present work is to investigate the effect of a prolonged leaching test (more than a year) on the microstructure of solidified cementitious wasteforms. A set of four different cement-based monoliths (Ap, Bp, Cp and Dp) was
Dmitry Tsvelikhovsky et al.
Journal of the American Chemical Society, 132(40), 14048-14051 (2010-09-23)
The Pd-catalyzed condensation of 2-bromostyrene and 2-chloroaniline derivatives yields stable diphenylamine intermediates, which are selectively converted to five-, six-, or seven-membered heteroaromatics (indoles, carbazoles, acridines, and dibenzazepines). The selectivity of these intramolecular transformations is uniquely ligand-controlled and offers efficient routes

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