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Catalog Number:
33523
CAS Number:
1892-57-5
N- (3-Diméthylaminopropyl) -N′- éthylcarbodiimide
Purity:
≥ 98% (CG)
Synonym(s):
1-(3-diméthylaminopropyl)-3-éthylcarbodiimide, N -Éthyl -N' -(3-diméthylaminopropyl)carbodiimide
Hazmat
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$20.00 /5G
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Product Information

Incompatible avec les acides forts et les agents oxydants forts. Le 1-(3-diméthylaminopropyl)-3-éthylcarbodiimide est utilisé comme agent d'activation carboxyle et active les groupes phosphate dans les mono et di esters phospho.

Synonyms
1-(3-diméthylaminopropyl)-3-éthylcarbodiimide, N -Éthyl -N' -(3-diméthylaminopropyl)carbodiimide
CAS Number
1892-57-5
Purity
≥ 98% (CG)
Molecular Formula
C8H17N3
Molecular Weight
155.24
MDL Number
MFCD00044916
PubChem ID
15908
Density
0,877 g/mL à 20 °C (Lit.)
Appearance
Liquide incolore à jaune clair
Boiling Point
100 - 105 ?C / 2 mmHg
Refractive Index
n20/D 1,459 - 1,465 (lit.)
Conditions
Conserver à -10 °C
General Information
Synonyms
1-(3-diméthylaminopropyl)-3-éthylcarbodiimide, N -Éthyl -N' -(3-diméthylaminopropyl)carbodiimide
CAS Number
1892-57-5
Purity
≥ 98% (CG)
Molecular Formula
C8H17N3
Molecular Weight
155.24
MDL Number
MFCD00044916
PubChem ID
15908
Density
0,877 g/mL à 20 °C (Lit.)
Appearance
Liquide incolore à jaune clair
Boiling Point
100 - 105 ?C / 2 mmHg
Refractive Index
n20/D 1,459 - 1,465 (lit.)
Conditions
Conserver à -10 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
Oui
Antibiotic
Non
DEA-regulated
Non
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