3,4-Diaminotoluene
3,4-Diaminotoluene structure
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Common Name | 3,4-Diaminotoluene | ||
|---|---|---|---|---|
| CAS Number | 496-72-0 | Molecular Weight | 122.168 | |
| Density | 1.1±0.1 g/cm3 | Boiling Point | 262.3±20.0 °C at 760 mmHg | |
| Molecular Formula | C7H10N2 | Melting Point | 87-89 °C(lit.) | |
| MSDS | Chinese USA | Flash Point | 132.1±21.3 °C | |
| Symbol |
GHS07 |
Signal Word | Warning | |
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Teratogenic evaluation of 2-nitro-p-phenylenediamine, 4-nitro-o-phenylenediamine, and 2,5-toluenediamine sulfate in the mouse.
Teratology 24(3) , 253-65, (1981) Pregnant outbred albino (CD-1) mice were given 2-nitro-p-phenylenediamine (2NPPD; 32-256 mg/kg/day), 4-nitro-o-phenylenediamine (4NOPD; 16-1024 mg/kg/day) or 2,5-toluenediamine sulfate (2,5TDS; 16-64 mg/kg/day) by subcutaneous injection on Days 6-15 of gestat... |
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Effect of 4 toluene diamine isomers on murine testicular DNA synthesis.
Mutat. Res. 91(1) , 75-9, (1981)
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Teratogenesis study of o-toluenediamine in rats and rabbits.
Toxicol. Appl. Pharmacol. 71(3) , 323-9, (1983) 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 was conducted with Dutch-Belted ... |
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Final amended report of the safety assessment of toluene-2,5-diamine, toluene-2,5-diamine sulfate, and toluene-3,4-diamine as used in cosmetics.
Int. J. Toxicol. 29(3 Suppl) , 61S-83S, (2010) 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... |
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The catalysis of the reduction of Zn (II) ions by 3, 4-diaminotoluene. Dalmata G.
Electrochim. Acta 42(9) , 1307-14, (1997)
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Synthesis and tuberculostatic activity of new benzimidazole derivatives. Foks H, et al.
Chem. Heterocycl. Comp. 42(5) , 611-14, (2006)
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Bridge cleavage of [{PhP(Se)(µ-Se)}2] by 1,2- C6H4(EH)(E'H) (E, E'=O or NH). X-ray crystal structure of PhP(Se)(NHC6H4NH-1,2). Bhattacharyya P, et al.
J. Organomet. Chem. 623(1) , 116-119, (2001)
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Some 4-substituted< i> o</i>-phenylenediamines as reagents for selenium. Tanaka M and Kawashima T.
Talanta 12(3) , 211-19, (1965)
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Spectrophotometric determination of selenium (IV) with 4-methyl-o-phenylenediamine based on piazselenol formation. Kartal S, et al.
J. Anal. Chem. 65(12) , 1221-27, (2010)
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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) , 349-59, (2010)
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