| Identification | More | [Name]
N-Methyl-1,2-benzenediamine dihydrochloride | [CAS]
25148-68-9 | [Synonyms]
2-METHYLAMINOANILINE HYDROCHLORIDE
N-METHYL-1,2-BENZENEDIAMINE DIHYDROCHLORIDE
N-METHYL-1,2-PHENYLENEDIAMINE DIHYDROCHLORIDE
N-METHYL-1,2-PHENYLENEDIAMINE HYDROCHLORIDE
N-METHYL-O-PHENLENEDIAMINE DIHYDROCHLORIDE
N-METHYL-O-PHENYLENEDIAMINE DIHYDROCHLORIDE
N-METHYL-O-PHENYLENEDIAMINE HYDROCHLORIDE
2-benzenediamine,n-methyl-dihydrochloride
N-methylbenzene-1,2-diamine dihydrochloride
N-methyl-O-phenlenediamine hydrochloride
N-Methyl-O-PhenylenediamineHcl
N-Methyl-o-phenylenediamine2HCl
N-METHYL-2-PHENYLENEDIAMINEDIHYDROCHLORIDE
N-METHYL-ORTHO-PHENYLENEDIAMINE2HCL
N-METHYL-ORTHO-PHENYLENEDIAMINEDIHYDROCHLORIDE
N1-methylbenzene-1,2-diamine dihydrochloride
1,2-Benzenediamine, N-methyl-, dihydrochloride
N-Methyl-o-phenylenediamine dihydrochloride ,98% | [EINECS(EC#)]
246-655-8 | [Molecular Formula]
C7H12Cl2N2 | [MDL Number]
MFCD00042021 | [Molecular Weight]
195.09 | [MOL File]
25148-68-9.mol |
| Chemical Properties | Back Directory | [Appearance]
Redish Powder | [Melting point ]
191°C | [storage temp. ]
Inert atmosphere,Room Temperature | [solubility ]
DMSO (Slightly), Methanol (Slightly) | [form ]
Solid | [color ]
Pale Red to Light Beige | [Water Solubility ]
>=10 g/100 mL at 23 ºC | [Detection Methods]
T,NMR | [InChI]
InChI=1S/C7H10N2.ClH/c1-9-7-5-3-2-4-6(7)8;/h2-5,9H,8H2,1H3;1H | [InChIKey]
IWRJMQUPCKSBFP-UHFFFAOYSA-N | [SMILES]
N(C1C=CC=CC=1N)C.Cl | [CAS DataBase Reference]
25148-68-9(CAS DataBase Reference) | [EPA Substance Registry System]
25148-68-9(EPA Substance) |
| Hazard Information | Back Directory | [General Description]
Crystals (from ethanol); light purple powder. | [Reactivity Profile]
N-METHYL-O-PHENYLENEDIAMINE DIHYDROCHLORIDE(25148-68-9) 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. | [Air & Water Reactions]
Water soluble. | [Fire Hazard]
Flash point data for this chemical are not available; however, N-METHYL-O-PHENYLENEDIAMINE DIHYDROCHLORIDE is probably combustible. | [Chemical Properties]
Redish Powder | [Uses]
N-Methyl-o-phenylenediamine, Dihydrochloride (cas# 25148-68-9) is a compound useful in organic synthesis. |
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