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272361

Sigma-Aldrich

2,3-Diaminotoluene

97%

Synonym(s):

3-Methyl-o-phenylenediamine

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About This Item

Linear Formula:
CH3C6H3(NH2)2
CAS Number:
2687-25-4
Molecular Weight:
122.17
Beilstein:
907184
EC Number:
220-248-5
MDL number:
MFCD00011589
UNSPSC Code:
12352100
PubChem Substance ID:
24856468

Quality Level

100

Assay

97%

mp

59-65 °C (lit.)

SMILES string

Cc1cccc(N)c1N

InChI

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

InChI key

AXNUJYHFQHQZBE-UHFFFAOYSA-N

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General description

The antitumour activity of Pd(II) and Pt(II) new complexes with 2,3-diaminotoluene was studied. 2,3-Diaminotoluene induced CYP1A activity.

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Classifications

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

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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M Pérez-Cabré et al.
Journal of inorganic biochemistry, 98(3), 510-521 (2004-02-28)
Pd(II) and Pt(II) new complexes with simple aromatic diamines were synthesised and characterised with the aim of studying their possible antitumour activity. The aromatic diamines chosen were 2,3-diaminotoluene (2,3 dat), 3,4-diaminotoluene (3,4 dat), 4,5-diaminoxylene (4,5 dax) and 2,3-diaminophenol (2,3 dap).
Y L Cheung et al.
Toxicology and applied pharmacology, 139(1), 203-211 (1996-07-01)
The present study was undertaken to provide a rationale for the marked difference in carcinogenic potential among isomeric diaminotoluenes, in relation to their ability to induce their own bioactivation through CYP1A induction, their genotoxic potential, and their ability to bind

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