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Merck

66770

Sigma-Aldrich

Methylenediamine dihydrochloride

≥98.0% (AT)

Sinónimos:

Diaminomethane dihydrochloride

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About This Item

Fórmula lineal:
CH2(NH2)2 · 2HCl
Número de CAS:
Peso molecular:
118.99
Beilstein:
3664689
Número CE:
Número MDL:
Código UNSPSC:
12352100
ID de la sustancia en PubChem:
NACRES:
NA.22
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Ensayo

≥98.0% (AT)

Formulario

solid

grupo funcional

amine

temp. de almacenamiento

2-8°C

cadena SMILES

Cl.Cl.NCN

InChI

1S/CH6N2.2ClH/c2-1-3;;/h1-3H2;2*1H

Clave InChI

QCYJCJJCNRIMNG-UHFFFAOYSA-N

Descripción general

Methylenediamine dihydrochloride, also known as Diaminomethane dihydrochloride is an organic compound that is often utilized as a reagent and slow ammonia-releasing agent during the synthesis of primary amides of peptides and amino acids from active esters. [1]

Aplicación

Methylenediamine dihydrochloride can be used as a reactant to synthesize:
  • Poly(methylene biguanides) via polycondensation reaction with sodium dicyanamide in the presence of 1-butanol[2].
  • Didodecanoylamides by reacting with (2S)-2-methyldodecanoyl chloride via acylation in the presence of sodium bicarbonate[3].
It can also be used as a hydrogen source in catalytic hydrogenation reactions[4].

Código de clase de almacenamiento

11 - Combustible Solids

Clase de riesgo para el agua (WGK)

WGK 3

Punto de inflamabilidad (°F)

Not applicable

Punto de inflamabilidad (°C)

Not applicable

Equipo de protección personal

Eyeshields, Gloves, type N95 (US)


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Nickel-catalyzed transfer semihydrogenation and hydroamination of aromatic alkynes using amines as hydrogen donors
Reyes S, et al.
Organometallics, 30, 3340-3345 (2011)
Takaaki Sumiyoshi et al.
Journal of the American Chemical Society, 125(40), 12137-12142 (2003-10-02)
A series of 10 didodecanoylamides of alpha,omega-alkylidenediamines bridged by a straight carbon chain varying in length from 0 to 9 carbons was examined as possible gelator molecules of organic liquids to gain information on the relationships between the spacial arrangement
G Galaverna et al.
International journal of peptide and protein research, 42(1), 53-57 (1993-07-01)
Amide formation from acids, N-protected amino acids and peptides was achieved in an easy and convenient way by treating "active esters" such as succinimidyl or 4-nitrophenyl esters or acyl chlorides with diaminomethane dihydrochloride in dioxane in the presence of Et3N.
Poly(alkylene biguanides) as proton conductors for high-temperature PEMFCs.
Jochen Britz et al.
Advanced materials (Deerfield Beach, Fla.), 22(8), E72-E76 (2010-03-11)
'Passe-partout effect' in positive patch test reactions: a novel pattern of edge effect.
Esen Ozkaya
Contact dermatitis, 61(4), 245-247 (2009-10-15)

Questions

  1. I am curious about where HCl is located and how it is bonded in the molecule.

    1 answer
    1. Both of the amino groups of the Methylenediamine are protonated (that is, as -NH3+ groups), with a chloride (Cl-) counterion associated with each of them. That is, it is best to think of the HCl as being dissociated, with H+ on the amine and Cl- as the counterion.

      Helpful?

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