N-(3-Dimethylaminopropyl)-N'-ethylcarbodiimide

95%

Reagent Code: #56659
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Alias 1-(3-Dimethylaminopropyl)-3-ethylcarbodiimide
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CAS Number 1892-57-5

science Other reagents with same CAS 1892-57-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 155.24 g/mol
Formula C₈H₁₇N₃
badge Registry Numbers
EC Number 217-579-2
MDL Number MFCD00044916
thermostat Physical Properties
Boiling Point 66-68°C/1mmHg
inventory_2 Storage & Handling
Density 0.877 g/mL at 20 °C(lit.)
Storage -20°C, sealed

description Product Description

Used extensively in peptide synthesis to facilitate the formation of amide bonds between amino acids. It is particularly effective in coupling carboxyl groups to amines, making it a crucial reagent in the production of peptides and proteins. Additionally, it finds application in the modification of polymers and surfaces, where it aids in the attachment of functional groups or biomolecules. In biochemistry, it is employed to crosslink proteins or nucleic acids, enabling the study of molecular interactions. Its role in activating carboxylic acids for further reactions also makes it valuable in organic synthesis, especially in the preparation of esters and amides.

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Test Parameter Specification
Purity (GC) 94.5-100%
Refractive Index (N20D) 1.459-1.463
Appearance Colorless to slightly greenish-yellow clear liquid
Infrared Spectrometry Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿320.00
inventory 5g
10-20 days ฿540.00
inventory 25g
10-20 days ฿1,630.00
inventory 100g
10-20 days ฿5,600.00
inventory 500g
10-20 days ฿18,700.00

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N-(3-Dimethylaminopropyl)-N'-ethylcarbodiimide
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Used extensively in peptide synthesis to facilitate the formation of amide bonds between amino acids. It is particularly effective in coupling carboxyl groups to amines, making it a crucial reagent in the production of peptides and proteins. Additionally, it finds application in the modification of polymers and surfaces, where it aids in the attachment of functional groups or biomolecules. In biochemistry, it is employed to crosslink proteins or nucleic acids, enabling the study of molecular interactions. Its role in activating carboxylic acids for further reactions also makes it valuable in organic synthesis, especially in the preparation of esters and amides.
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