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Safety Information

236322

Sigma-Aldrich

2-Chloro-4-aminotoluene

98%

Synonym(s):

3-Chloro-4-methylaniline, 3-Chloro-p-toluidine, 4-Amino-2-chlorotoluene

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About This Item

Linear Formula:
ClC6H3(CH3)NH2
CAS Number:
95-74-9
Molecular Weight:
141.60
Beilstein:
636511
EC Number:
202-446-3
MDL number:
MFCD00007773
UNSPSC Code:
12352100
PubChem Substance ID:
24854163
NACRES:
NA.22

Quality Level

100

Assay

98%

form

solid

refractive index

n20/D 1.584 (lit.)

bp

237-238 °C (lit.)

mp

24-25 °C (lit.)

density

1.167 g/mL at 25 °C

functional group

chloro

storage temp.

2-8°C

SMILES string

Cc1ccc(N)cc1Cl

InChI

1S/C7H8ClN/c1-5-2-3-6(9)4-7(5)8/h2-4H,9H2,1H3

InChI key

RQKFYFNZSHWXAW-UHFFFAOYSA-N

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Application

2-Chloro-4-aminotoluene has been used in the preparation of 2-chloro-4-cyanotoluene by Sandmeyer reaction with cuprous cyanide.

Pictograms

Skull and crossbonesEnvironment
GHS06,GHS09

Signal Word

Danger

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 3 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Irrit. 2 - Skin Irrit. 2 - Skin Sens. 1

Storage Class Code

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 3

Flash Point(F)

212.0 °F - closed cup

Flash Point(C)

100 °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.

JAN Code

236322-BULK:
236322-VAR:
236322-500G:
236322-50G:

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Certificates of Analysis (COA)

Lot/Batch Number
MKCL6954
MKCK6313
10128PH
02827PH
04927LE

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119. Synthesis of nuclear amidino-derivatives of 5-aminoacridine.
Goldberg AA and Kelly W.
Journal of the Chemical Society, 637-641 (1947)
Randal S Stahl et al.
Journal of agricultural and food chemistry, 50(4), 732-738 (2002-02-07)
A method using a deuterated surrogate of the avicide 3-chloro-p-toluidine hydrochloride (CPTH) was developed to quantify the CPTH residues in the gastrointestinal (GI) tract and breast muscle tissues in birds collected in CPTH-baited sunflower and rice fields. This method increased
John J Johnston et al.
Pest management science, 61(7), 649-659 (2005-03-05)
A probabilistic model was developed to estimate target and non-target avian mortality associated with the application of the avicide CPTH (3-chloro-p-toluidine hydrochloride) to minimize sprouting rice damage in the southern USA. CPTH exposures for individual birds were predicted by random
E Nikodémusz et al.
Gegenbaurs morphologisches Jahrbuch, 128(5), 753-761 (1982-01-01)
Gross and microscopic changes in response to single po. doses of avicide 3-chloro-4-methyl benzamine HCl were studied in rooks (Corvus frugilegus L.) and pheasants (Phasianus colchicus L.). The observed changes followed a dose- and survival time related pattern and rooks
Angshuman Bagchi et al.
Computational biology and chemistry, 30(3), 227-232 (2006-05-25)
Microbial redox reactions involving inorganic sulfur compounds in the environment are one of the major reactions of the global sulfur cycle. These reactions are mediated by phylogenetically diverse prokaryotes containing the sulfur oxidizing gene cluster (sox). The sox gene cluster
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