Discover the new Chem-Impex: Where innovation starts with a bond.

Catalog Number:
33523
CAS Number:
1892-57-5
N-(3-Dimethylaminopropyl)-N′-ethylcarbodiimide
Purity:
≥ 98% (GC)
Synonym(s):
1-(3-Dimethylaminopropyl)-3-ethylcarbodiimide, N-Ethyl-N'-(3-dimethylaminopropyl)carbodiimide
Hazmat
Documents
$20.00 /5G
Pack Size Availability Price
Request Bulk Quote
Product Information

Incompatible with strong acids and strong oxidizing agents. 1-(3-Dimethylaminopropyl)-3-ethylcarbodiimide is used as a carboxyl activating agent and activate phosphate groups in phospho mono and di esters.

Synonyms
1-(3-Dimethylaminopropyl)-3-ethylcarbodiimide, N-Ethyl-N'-(3-dimethylaminopropyl)carbodiimide
CAS Number
1892-57-5
Purity
≥ 98% (GC)
Molecular Formula
C8H17N3
Molecular Weight
0
MDL Number
MFCD00044916
PubChem ID
15908
Density
0.877 g/mL at 20 °C (Lit.)
Appearance
Colorless to light yellow liquid
Boiling Point
100 - 105 °C / 2 mmHg
Refractive Index
n20/D 1.459 - 1.465 (Lit.)
Conditions
Store at -10 °C
General Information
Synonyms
1-(3-Dimethylaminopropyl)-3-ethylcarbodiimide, N-Ethyl-N'-(3-dimethylaminopropyl)carbodiimide
CAS Number
1892-57-5
Purity
≥ 98% (GC)
Molecular Formula
C8H17N3
Molecular Weight
0
MDL Number
MFCD00044916
PubChem ID
15908
Density
0.877 g/mL at 20 °C (Lit.)
Appearance
Colorless to light yellow liquid
Boiling Point
100 - 105 °C / 2 mmHg
Refractive Index
n20/D 1.459 - 1.465 (Lit.)
Conditions
Store at -10 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
Yes
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

N-(3-Dimethylaminopropyl)-N'-ethylcarbodiimide is widely utilized in research focused on:

  • Peptide Synthesis: This compound is a key reagent in the formation of peptide bonds, facilitating the coupling of amino acids in the development of peptides and proteins, which are essential in pharmaceuticals and biotechnology.
  • Bioconjugation: It is commonly used to link biomolecules, such as proteins to antibodies or drugs, enhancing the efficacy of targeted therapies in drug development and diagnostics.
  • Polymer Chemistry: The chemical serves as a coupling agent in the synthesis of various polymers, improving their properties for applications in materials science and engineering.
  • Cross-linking Agents: It acts as a cross-linker in the preparation of hydrogels, which are vital in tissue engineering and drug delivery systems, offering controlled release of therapeutic agents.
  • Surface Modification: This compound is employed in modifying surfaces of biomaterials to enhance biocompatibility, crucial for medical implants and devices.

Citations