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Merck

89650

Sigma-Aldrich

p-Toluidin -hydrochlorid

purum, ≥99.0% (AT)

Synonym(e):

4-Methyl-anilin -hydrochlorid

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About This Item

Lineare Formel:
CH3C6H4NH2 · HCl
CAS-Nummer:
Molekulargewicht:
143.61
Beilstein:
3557540
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
12352100
PubChem Substanz-ID:
NACRES:
NA.22

Qualität

purum

Qualitätsniveau

Assay

≥99.0% (AT)

Form

crystals

mp (Schmelzpunkt)

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

InChIKey

JQKBUTDZZRGQDR-UHFFFAOYSA-N

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Verwandte Kategorien

Signalwort

Danger

Gefahreneinstufungen

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

Lagerklassenschlüssel

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

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

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


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In der Dokumentenbibliothek finden Sie die Dokumentation zu den Produkten, die Sie kürzlich erworben haben.

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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
Issam Ahmed Mohammed et al.
Molecules (Basel, Switzerland), 15(10), 7498-7509 (2010-10-27)
Maleic anhydride was reacted with p-aminophenol and p-toluidine in the presence of di-phosphorus pentoxide (P₂O₅) as a catalyst to produce two compounds: N-(4-hydroxy-phenyl)maleimide (I) and N-(4-methylphenyl)maleimide (II). The new azo compounds I(a-c) and II(a-c) were prepared by the reaction of
E A Kowaluk et al.
Journal of pharmaceutical sciences, 75(6), 562-570 (1986-06-01)
Aqueous solutions of several ionizable substances were stored in plastic infusion bags and the sorption of the substances monitored with time. The substances used were p-nitrophenol, p-toluidine, warfarin sodium [3-(alpha-acetonylbenzyl)-4-hydroxycoumarin sodium salt] and trifluoperazine hydrochloride (10-[3-(4-methyl-1-piperazinyl)propyl]-2-(trifluoromethyl)phenothiazine dihydrochloride). The rate and
Paul G Stevenson et al.
Journal of chromatography. A, 1218(45), 8255-8263 (2011-10-11)
Several simple techniques are presented for the identification of the boundaries of chromatographic peaks. These methods provide a significant reduction in the time needed to perform the rapid, automatic calculation of the central peak moments and to evaluate the quality
N Dharaiya et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 93, 306-312 (2012-04-10)
The effect of p-toluidine (PTD) on the growth of cationic surfactant micelles in aqueous solutions was examined by viscosity, UV-visible spectroscopy, dynamic light scattering (DLS), (1)H NMR and nuclear Overhauser effect spectroscopy (NOESY). Viscosity and scattering results are used to

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