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33380

Sigma-Aldrich

4-Methyl-o-phenylendiamin

purum, ≥98.0% (NT)

Synonym(e):

3,4-Diamino-toluol

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About This Item

Lineare Formel:
CH3C6H3(NH2)2
CAS-Nummer:
496-72-0
Molekulargewicht:
122.17
Beilstein:
507965
EG-Nummer:
207-826-2
MDL-Nummer:
MFCD00007728
UNSPSC-Code:
12352100
PubChem Substanz-ID:
329754508
NACRES:
NA.22

Qualität

purum

Qualitätsniveau

100

Assay

≥98.0% (NT)

bp

155-156 °C/18 mmHg (lit.)

mp (Schmelzpunkt)

87-89 °C (lit.)
87-89 °C

Anwendung(en)

agriculture
environmental

SMILES String

Cc1ccc(N)c(N)c1

InChI

1S/C7H10N2/c1-5-2-3-6(8)7(9)4-5/h2-4H,8-9H2,1H3

InChIKey

DGRGLKZMKWPMOH-UHFFFAOYSA-N

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Allgemeine Beschreibung

4-Methyl-o-phenylenediamine is the 4-substituted derivative of o-phenylenediamine. It reacts with selenous acid in acid solution to form benzoselenadiazoles.

Anwendung

4-Methyl-o-phenylenediamine was employed as chromogenic reagent in the spectrophotometric determination of selenium(IV). It was used in the synthesis of an asymmetrical tetradentate Schiff base via condensation with dehydroacetic acid and salicylic aldehyde.

Piktogramme

Exclamation mark
GHS07

Signalwort

Warning

Gefahreneinstufungen

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Zielorgane

Respiratory system

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 1

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

dust mask type N95 (US), Eyeshields, Gloves

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Analysenzertifikate (COA)

Lot/Batch Number
BCBG0032V
1401133V
BCBB4968
8158X
1401133

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Synthesis, characterization and thermal study of some transition metal complexes of an asymmetrical tetradentate Schiff base ligand.
Munde AS, et al.
J. Serb. Chem. Soc., 75(3), 349-359 (2010)
Spectrophotometric determination of selenium (IV) with 4-methyl-o-phenylenediamine based on piazselenol formation.
Kartal S, et al.
Journal of Analytical Chemistry, 65(12), 1221-1227 (2010)
Some 4-substituted< i> o</i>-phenylenediamines as reagents for selenium.
Tanaka M and Kawashima T.
Talanta, 12(3), 211-219 (1965)
P J Becci et al.
Toxicology and applied pharmacology, 71(3), 323-329 (1983-12-01)
o-Toluenediamine in corn oil was administered po to Sprague-Dawley rats at dosages of 10, 30, 100, or 300 mg/kg body wt/day during Days 6 through 15 of gestation. All animals were killed on Day 20 of gestation. A similar study
Christina L Burnett et al.
International journal of toxicology, 29(3 Suppl), 61S-83S (2010-05-22)
Toluene-2,5-diamine, toluene-2,5-diamine sulfate, and toluene-3,4-diamine are diaminotoluenes used as colorants in permanent hair dyes and tints. Toluene-2,5-diamine is used in 79 products at concentrations up to 3%; toluene-2,5-diamine sulfate is used in 168 products at concentrations up to 4%. Toluene-3,4-diamine
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