N-Methyl-1,2-benzenediamine dihydrochloride

1,2-Benzenediamine, N1-methyl-, hydrochloride (1:2)

1,2-Benzenediamine,N1-methyl-,hydrochloride (1:2);1,2-Benzenediamine,N-methyl-,dihydrochloride;o-Phenylenediamine,N-methyl-,dihydrochloride;N-Methyl-o-phenylenediamine dihydrochloride;N-Methyl-1,2-diaminobenzene dihydrochloride;N-Methyl-1,2-phenylenediamine dihydrochloride;1-Amino-2-methylaminobenzene dihydrochloride;N-Methyl-1,2-benzenediamine dihydrochloride;2-(Methylamino)aniline Dihydrochloride

25148-68-9

C7H10N2.2ClH

InChIKey=DKEONVNYXODZRQ-UHFFFAOYSA-N

195.09000

194.03800

246-655-8

NML5KQ540I

DTXSID5025651

2921519090

Bulk Drug Intermediates

38.05000

Crystals (from ethanol); light purple powder. (NTP, 1992)

191ºC

252.4ºC at 760 mmHg

122.4ºC

H2O: >=10 g/100 mL at 23 ºC

Keep container closed when not in use. Store in a tightly closed container. Store in a cool, dry, well-ventilated area away from

0.0193mmHg at 25°C

Water soluble.

Salts, Acidic

N-METHYL-O-PHENYLENEDIAMINE DIHYDROCHLORIDE is an acidic salt. Materials in this group are generally soluble in water. The resulting solutions contain moderate concentrations of hydrogen ions and have pH's of less than 7.0. They react as acids to neutralize bases. These neutralizations generate heat, but less or far less than is generated by neutralization of inorganic acids, inorganic oxoacids, and carboxylic acid. They usually do not react as either oxidizing agents or reducing agents but such behavior is not impossible. Many of these compounds catalyze organic reactions.