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33380

Sigma-Aldrich

4-Methyl-o-phenylenediamine

purum, ≥98.0% (NT)

Sinonimo/i:

3,4-Toluenediamine

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About This Item

Formula condensata:
CH3C6H3(NH2)2
Numero CAS:
496-72-0
Peso molecolare:
122.17
Beilstein:
507965
Numero CE:
207-826-2
Numero MDL:
MFCD00007728
Codice UNSPSC:
12352100
ID PubChem:
329754508
NACRES:
NA.22

Grado

purum

Livello qualitativo

100

Saggio

≥98.0% (NT)

P. ebollizione

155-156 °C/18 mmHg (lit.)

Punto di fusione

87-89 °C (lit.)
87-89 °C

applicazioni

agriculture
environmental

Stringa SMILE

Cc1ccc(N)c(N)c1

InChI

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

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Categorie correlate

Descrizione generale

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

Applicazioni

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.

Pittogrammi

Exclamation mark
GHS07

Avvertenze

Warning

Indicazioni di pericolo

H302 + H312 + H332,H315,H319,H335

Classi di pericolo

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

Organi bersaglio

Respiratory system

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 1

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

dust mask type N95 (US), Eyeshields, Gloves

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Certificati d'analisi (COA)

Lot/Batch Number

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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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