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Merck
CN

236322

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
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24854163
EC Number:
202-446-3
Beilstein/REAXYS Number:
636511
MDL number:
MFCD00007773

Key Documents

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Product Name

2-Chloro-4-aminotoluene, 98%

InChI key

RQKFYFNZSHWXAW-UHFFFAOYSA-N

InChI

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

SMILES string

Cc1ccc(N)cc1Cl

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

Quality Level

100

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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

signalword

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

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

ppe

Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges

Regulatory Information

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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)
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
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
Randal S Stahl et al.
Journal of chromatographic science, 43(7), 367-371 (2005-09-24)
Methods are developed to extract and quantitate the avicide 3-chloro-p-toluidine hydrochloride (CPT HCl) from rough-hulled rice and ethyl-cellulose-coated rice baits using high-performance liquid chromatography. The mobile phase used in the ethyl-cellulose-coated rice matrix method is an acetonitrile(ACN)-phosphate buffer (60:40) at
J C Hurley et al.
Journal of agricultural and food chemistry, 47(7), 2904-2907 (1999-12-20)
Stabilization of the avicide 3-chloro-p-toluidine (CPTH) on rice baits by pseudo latex polymeric coating and beta-cyclodextin inclusion was investigated. When CPTH-treated rice baits were exposed to sunlight, the CPTH formed colored compounds, which exacerbated problems with bait acceptance and efficacy.
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