DIMETHYLAMMONIUM DIMETHYLCARBAMATE(DIMCARB) Chemical Properties

Melting point:

°C

Boiling point:

60-61 °C(lit.)

Density 

1.05 g/mL at 25 °C(lit.)

refractive index 

n20/D 1.454(lit.)

Flash point:

150 °F

storage temp. 

2-8°C

solubility 

Chloroform (Sparingly), Methanol (Slightly), Water (Soluble)

form 

Liquid

Specific Gravity

1.05

color 

Clear colorless to light yellow

BRN 

4531667

EPA Substance Registry System

Dimethylammonium dimethylcarbamate (4137-10-4)

Safety Information

Hazard Codes 

Xi

Risk Statements 

10-36/37/38

Safety Statements 

26-36

RIDADR 

2733

WGK Germany 

3

F 

4.4

HS Code 

29215990

MSDS

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• Language:English Provider:ACROS

DIMETHYLAMMONIUM DIMETHYLCARBAMATE(DIMCARB) Usage And Synthesis

Chemical Properties

clear colorless to light yellow liquid

Uses

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

Uses

Dimethylammonium dimethylcarbamate is an ionic liquid primarily used as a solvent.• ;For synthesis of calixarene-based ketocyanine fluorophores1• ;Distillation extraction of tannins from plant materials2• ;Electrodeposition of silver3 or of lead on glassy carbon and mercury film electrodes4• ;Synthesis of Ag and Au nanostructures5• ;Reusable reaction medium for synthesis of monoarylidene cyclopentanones6

General Description

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.

DIMETHYLAMMONIUM DIMETHYLCARBAMATE(DIMCARB)(4137-10-4)Related Product Information

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• Z-ARG(Z)2-OH
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• Z-PRO-D-LEU-OH
• Z-PRO-PHE-OH
• Z-PRO-MET-OH
• BOC-N-ME-P-NITRO-PHE-OH DCHA
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• BOC-PRO-LEU-VAL-OME
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• AMO 1618
• Z-PRO-ILE-OH
• ASISCHEM D08269
• Z-PRO-PHE-NH2