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N-Methyl-1,2-benzenediamine dihydrochloride

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N-Methyl-1,2-benzenediamine dihydrochloride Basic information

Product Name:
N-Methyl-1,2-benzenediamine dihydrochloride
Synonyms:
  • 2-METHYLAMINOANILINE HYDROCHLORIDE
  • N-METHYL-O-PHENLENEDIAMINE DIHYDROCHLORIDE
  • N-METHYL-O-PHENYLENEDIAMINE DIHYDROCHLORIDE
  • N-METHYL-O-PHENYLENEDIAMINE HYDROCHLORIDE
  • N-METHYL-1,2-PHENYLENEDIAMINE DIHYDROCHLORIDE
  • N-METHYL-1,2-PHENYLENEDIAMINE HYDROCHLORIDE
  • N-METHYL-1,2-BENZENEDIAMINE DIHYDROCHLORIDE
  • 2-benzenediamine,n-methyl-dihydrochloride
CAS:
25148-68-9
MF:
C7H11ClN2
MW:
158.63
EINECS:
246-655-8
Product Categories:
  • Aromatics
  • Aromatics Compounds
  • Chemical intermediate for Telmisartan
  • INTERMEDIATESOF
  • 25148-68-9
Mol File:
25148-68-9.mol
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N-Methyl-1,2-benzenediamine dihydrochloride Chemical Properties

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
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
N-Methyl-o-phenylenediamine dihydrochloride (25148-68-9)
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Safety Information

Safety Statements 
24/25
RIDADR 
UN 2811 6.1/PG III
HazardClass 
IRRITANT
PackingGroup 
III
HS Code 
29214400

MSDS

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N-Methyl-1,2-benzenediamine dihydrochloride Usage And Synthesis

Chemical Properties

Redish Powder

Uses

N-Methyl-o-phenylenediamine, Dihydrochloride (cas# 25148-68-9) is a compound useful in organic synthesis.

General Description

Crystals (from ethanol); light purple powder.

Air & Water Reactions

Water soluble.

Reactivity Profile

N-Methyl-1,2-benzenediamine 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.

Fire Hazard

Flash point data for N-Methyl-1,2-benzenediamine dihydrochloride are not available; however, N-Methyl-1,2-benzenediamine dihydrochloride is probably combustible.

N-Methyl-1,2-benzenediamine dihydrochlorideSupplier

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