Dimethylcarbamoyl chloride
97%
Reagent
Code: #122093
Alias
Dimethylcarbamoyl chloride; chlorodimethylcarbamoyl, N,N-dimethylcarbamoyl chloride, chloroformyl dimethylamine, N,N-dimethylformyl chloride
CAS Number
79-44-7
blur_circular Chemical Specifications
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Molecular Information
Weight
107.54 g/mol
Formula
C₃H₆ClNO
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Registry Numbers
EC Number
201-208-6
MDL Number
MFCD00000635
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Physical Properties
Melting Point
−33 °C(lit.)
Boiling Point
167-168 °C775 mm Hg(lit.)
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Storage & Handling
Density
1.168 g/mL at 25 °C(lit.)
Storage
room temperature, dry
description Product Description
Used primarily in organic synthesis, it serves as a key reagent for introducing the dimethylcarbamoyl group into various compounds. It is widely employed in the production of pharmaceuticals, particularly in the synthesis of active pharmaceutical ingredients (APIs) that require carbamate functionalities. Additionally, it finds application in the manufacture of agrochemicals, such as pesticides and herbicides, where it acts as an intermediate in the synthesis of carbamate-based compounds. Its role in polymer chemistry is also notable, as it is used to modify polymers to enhance specific properties. Due to its reactivity, it is handled with caution in controlled environments to ensure safety.
format_list_bulleted Product Specification
Test Parameter | Specification |
---|---|
Purity (GC) | 97-100 |
Refractive Index (N20/D) | 1.452-1.455 |
Specific Gravity (20/20°C) | 1.169-1.712 |
Appearance | Colorless Liquid |
Infrared Spectrum | Conforms To Structure |
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Dimethylcarbamoyl chloride
Used primarily in organic synthesis, it serves as a key reagent for introducing the dimethylcarbamoyl group into various compounds. It is widely employed in the production of pharmaceuticals, particularly in the synthesis of active pharmaceutical ingredients (APIs) that require carbamate functionalities. Additionally, it finds application in the manufacture of agrochemicals, such as pesticides and herbicides, where it acts as an intermediate in the synthesis of carbamate-based compounds. Its role in polymer chemistry is also notable, as it is used to modify polymers to enhance specific properties. Due to its reactivity, it is handled with caution in controlled environments to ensure safety.
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