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89650

p-Toluidine hydrochloride

Name: <I>p</I>-Toluidine hydrochloride
Brand: SIAL

purum, ≥99.0% (AT)

Synonym(s):

4-Methylaniline hydrochloride

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About This Item

Linear Formula:

CH₃C₆H₄NH₂· HCl

CAS Number:

540-23-8

Molecular Weight:

143.61

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

329769758

EC Number:

208-740-8

Beilstein/REAXYS Number:

3557540

MDL number:

MFCD00035497

Assay:

≥99.0% (AT)

Form:

crystals

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Properties

grade

purum

Quality Level

100

assay

≥99.0% (AT)

form

crystals

mp

243-245 °C (lit.)

SMILES string

Cl[H].Cc1ccc(N)cc1

InChI

1S/C7H9N.ClH/c1-6-2-4-7(8)5-3-6;/h2-5H,8H2,1H3;1H

InChI key

JQKBUTDZZRGQDR-UHFFFAOYSA-N

Description

pictograms

GHS06,GHS08,GHS09

signalword

Danger

hcodes

H301 + H311 + H331,H317,H319,H351,H410

pcodes

P273 - P280 - P301 + P310 - P302 + P352 + P312 - P304 + P340 + P311 - P305 + P351 + P338

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Carc. 2 - Eye 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

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges

Regulatory Information

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Distinct differences in the mechanisms of mucosal damage and γ-H2AX formation in the rat urinary bladder treated with o-toluidine and o-anisidine.

Takeshi Toyoda et al.

Archives of toxicology, 93(3), 753-762 (2019-01-19)

Although aromatic amines are widely used as raw materials for dyes, some of them have been concerned about carcinogenicity in the urinary bladder. We examined early changes in histopathology and the formation of γ-H2AX, a biomarker of DNA damage, in

Mutagenic potential of some chemical components of dental materials.

E G Miller et al.

Dental materials : official publication of the Academy of Dental Materials, 2(4), 163-165 (1986-08-01)

Spectrophotometric and spectroscopic studies of charge transfer complexes of p-toluidine as an electron donor with picric acid as an electron acceptor in different solvents.

Neeti Singh et al.

Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 75(4), 1347-1353 (2010-02-09)

The charge transfer complexes of the donor p-toluidine with pi-acceptor picric acid have been studied spectrophotometrically in various solvents such as carbon tetrachloride, chloroform, dichloromethane acetone, ethanol, and methanol at room temperature using absorption spectrophotometer. The results indicate that formation

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Global Trade Item Number

SKU	GTIN
89650-100G	04061833076392
89650-500G	04061833076408