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408395

Sigma-Aldrich

Dimethylammoniumdimethylcarbamat

Synonym(e):

N-Methylmethanamin-dimethylcarbamat, Dimcarb, Dimethylamin Kohlendioxid Komplex

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About This Item

Lineare Formel:
(CH3)2NH · (CH3)2NCOOH
CAS-Nummer:
Molekulargewicht:
134.18
Beilstein:
4531667
MDL-Nummer:
UNSPSC-Code:
12352100
PubChem Substanz-ID:
NACRES:
NA.22

Form

liquid

Qualitätsniveau

Brechungsindex

n20/D 1.454 (lit.)

bp

60-61 °C (lit.)

Dichte

1.05 g/mL at 25 °C (lit.)

Funktionelle Gruppe

amine

SMILES String

CNC.CN(C)C(O)=O

InChI

1S/C3H7NO2.C2H7N/c1-4(2)3(5)6;1-3-2/h1-2H3,(H,5,6);3H,1-2H3

InChIKey

JIYXHCMRGZVYMA-UHFFFAOYSA-N

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Allgemeine Beschreibung

Dimethylammonium dimethylcarbamate (DIMCARB) is the carbamate salt of dimethylamine. It is widely used as solvent and extractant. It has been investigated as ionic liquid. DIMCARB is formed by the reaction of dimethylamine and carbon dioxide.

Anwendung

Dimethylammonium dimethylcarbamate (DIMCARB) may be employed as an equivalent of dimethylamine, which on reaction with carboxylic acids affords N,N-dimethyl amides. It may be employed as ionic liquid for the synthesis of Cup-shaped calix[4]arenes bearing one or two ketocyanine fluorophore fragments at the wide rim of the macrocycle.
Ionic liquid primarily used as a solvent.
  • For synthesis of calixarene-based ketocyanine fluorophores
  • Distillation extraction of tannins from plant materials
  • Electrodeposition of silver or of lead on glassy carbon and mercury film electrodes
  • Synthesis of Ag and Au nanostructures
  • Reusable reaction medium for synthesis of monoarylidene cyclopentanones

Signalwort

Danger

Gefahreneinstufungen

Acute Tox. 4 Inhalation - Eye Dam. 1 - Flam. Liq. 2 - Skin Irrit. 2 - STOT SE 3

Zielorgane

Respiratory system

Lagerklassenschlüssel

3 - Flammable liquids

WGK

WGK 3

Flammpunkt (°F)

55.4 °F - DIN 51758

Flammpunkt (°C)

13 °C - DIN 51758

Persönliche Schutzausrüstung

Eyeshields, Faceshields, Gloves


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Lam Phan et al.
The Journal of organic chemistry, 73(1), 127-132 (2007-12-11)
Known liquids that can reversibly switch their polarity at atmospheric pressure are all prepared as mixtures of two liquid components; we now report a series of switchable-polarity solvents that consist, in their low-polarity form, of only a single liquid component
Dimethylammonium dimethylcarbamate (DIMCARB) as solvent and extractant.
Schroth W, et al.
Z. Chem., 73(1), 127-132 (1989)
Synthesis of calixarene-based ketocyanine fluorophores.
Matvieiev Y, et al.
Tetrahedron Letters, 52(30), 3922-3925 (2011)
Direct Catalytic Formation of Primary and Tertiary Amides from Non-Activated Carboxylic Acids, Employing Carbamates as Amine Source.
Tinnis F, et al.
Advanced Synthesis & Catalysis, 354(13), 2531-2536 (2012)
K M Johansson et al.
Physical chemistry chemical physics : PCCP, 10(20), 2972-2978 (2008-05-14)
We describe a fluidity and conductivity study as a function of composition in N-methylpyrrolidine-acetic acid mixtures. The simple 1 : 1 acid-base mixture appears to form an ionic liquid, but its degree of ionicity is quite low and such liquids

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