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Catalog Number:
00051
CAS Number:
530-62-1
N,N-Carbonyldiimidazole
Purity:
≥ 97% (Assay by titration)
Synonym(s):
CDI, 1,1'-Carbonyldiimidazole
Hazmat
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$18.50 /25G
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Product Information

N,N-Carbonyldiimidazole is a versatile reagent widely utilized in organic synthesis and peptide coupling reactions. Known for its efficiency in activating carboxylic acids, this compound facilitates the formation of amide bonds, making it an essential tool for chemists in the pharmaceutical and biotechnology industries. Its ability to promote reactions under mild conditions enhances its appeal, particularly in the synthesis of complex molecules, including pharmaceuticals and biologically active compounds.

Additionally, N,N-Carbonyldiimidazole serves as a coupling agent in the synthesis of various polymers and materials, contributing to advancements in material science. Its unique properties allow for selective reactions, minimizing by-products and improving yields, which is crucial for researchers aiming for high purity in their products. With its broad applicability and effectiveness, N,N-Carbonyldiimidazole stands out as a reliable choice for professionals seeking to streamline their synthetic processes and achieve superior results.

Synonyms
CDI, 1,1'-Carbonyldiimidazole
CAS Number
530-62-1
Purity
≥ 97% (Assay by titration)
Molecular Formula
C7H6N4O
Molecular Weight
162.15
MDL Number
MFCD00005286
PubChem ID
68263
Melting Point
113 - 124 ?C
Appearance
Off-white to yellowish brown crystalline powder
Conditions
Store at RT
General Information
Synonyms
CDI, 1,1'-Carbonyldiimidazole
CAS Number
530-62-1
Purity
≥ 97% (Assay by titration)
Molecular Formula
C7H6N4O
Molecular Weight
162.15
MDL Number
MFCD00005286
PubChem ID
68263
Melting Point
113 - 124 ?C
Appearance
Off-white to yellowish brown crystalline powder
Conditions
Store at RT
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Yes
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

N,N-Carbonyldiimidazole is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as an effective coupling agent in the formation of peptide bonds, facilitating the synthesis of peptides in pharmaceutical research.
  • Carbamate Formation: It is commonly used to convert alcohols into carbamates, which are important intermediates in the production of various agrochemicals and pharmaceuticals.
  • Protein Modification: Researchers employ it for selective modification of amino acids in proteins, enhancing the study of protein function and interactions.
  • Organic Synthesis: The compound acts as a versatile reagent in organic synthesis, particularly in the preparation of imidazole derivatives, which are valuable in medicinal chemistry.
  • Bioconjugation: It is utilized in bioconjugation processes to link biomolecules, aiding in the development of targeted drug delivery systems and diagnostic tools.

Citations