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

95%

  • Product Code: 56659
  Alias:    1-(3-Dimethylaminopropyl)-3-ethylcarbodiimide
  CAS:    1892-57-5
Molecular Weight: 155.24 g./mol Molecular Formula: C₈H₁₇N₃
EC Number: 217-579-2 MDL Number: MFCD00044916
Melting Point: Boiling Point: 66-68°C/1mmHg
Density: 0.877 g/mL at 20 °C(lit.) Storage Condition: -20°C, sealed
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.
Product Specification:
Test 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
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
1.000 10-20 days $16.07
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5.000 10-20 days $27.12
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25.000 10-20 days $81.87
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100.000 10-20 days $281.27
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500.000 10-20 days $939.23
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N-(3-Dimethylaminopropyl)-N'-ethylcarbodiimide
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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