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89650

Sigma-Aldrich

p-Toluidine hydrochloride

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
Beilstein:
3557540
EC Number:
208-740-8
MDL number:
MFCD00035497
UNSPSC Code:
12352100
PubChem Substance ID:
329769758
NACRES:
NA.22

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

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Related Categories

Signal Word

Danger

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 Code

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

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCCK3169
BCCF6475
BCCC3560
BCCC3031
BCCB5768

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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
Xiujuan Liu et al.
Journal of separation science, 30(15), 2506-2512 (2007-09-01)
In this study, two microextraction methods, viz. continuous-flow microextraction (CFME) and static liquid-phase microextraction (s-LPME), were optimized and compared for the determination of p-toluidine in water and Chlamydomonas reinhardtii samples. The calibration curve for p-toluidine was linear in the concentration
W J Brock et al.
Toxicology letters, 54(2-3), 317-325 (1990-12-01)
The in vivo covalent binding of ortho- and para-toluidine (OT and PT) to rat hepatic macromolecules was investigated to determine if a relationship exists between the degree of binding for each isomer and its carcinogenic potency. The ortho-isomer has been
Jingyan Zhang et al.
Journal of colloid and interface science, 316(2), 796-802 (2007-10-02)
The kinetics and mechanism of sphere-to-rod transitions of sodium alkyl sulfate micelles induced by hydrotropic salt, p-toluidine hydrochloride (PTHC), were investigated by stopped-flow with light scattering detection. Spherical sodium dodecyl sulfate (SDS) micelles transform into short ellipsoidal shapes at low
D R Doerge et al.
Chemical research in toxicology, 4(5), 556-560 (1991-09-01)
The metabolism of three arylamine substrates by H2O2 in the presence of each of the peroxidative enzymes chloroperoxidase (CPX) and pea seed peroxygenase (PSM) was conducted with normal H2O2 and with 18O-labeled H2O2. The resulting C-nitroso aromatic metabolites were examined
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