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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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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
Hao Wu et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 67(3-4), 976-979 (2007-02-03)
The molecular interactions between aniline, p-toluidines, benzidine and p-phenylenediamine as electron donors and 7,7,8,8-tetracyanoquinodimethane (TCNQ) as acceptor have been investigated by spectrophotometric method. Different variables affecting the reaction were studies and optimized. At the optimum reaction conditions Beer's law was
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
Svetlana N Ignatieva et al.
Inorganic chemistry, 49(12), 5407-5412 (2010-05-28)
The first representative of 1,5-diaza-3,7-diphosphacyclooctanes (1) with chiral L-menthyl substituents on the phosphorus atoms was obtained by condensation of L-menthylphosphine with formaldehyde and p-toluidine. This optically active cyclic bisphosphine readily forms a stable P,P-complex with borane (2) and P,P-chelate complexes
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