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Catalog Number:
41015
CAS Number:
64019-57-4
Tris(2-benzimidazolylméthyl)amine
Purity:
≥ 96 % (HPLC)
Synonym(s):
N,N-Bis(1H-benzimidazol-2-ylméthyl)-1H-benzimidazole-2-méthanamine, (BimH)3
Documents
$112.57 /200 mg
Taille
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Informations sur le produit

Tris(2-benzimidazolylmethyl)amine is a versatile compound recognized for its unique chelating properties, making it an essential choice in various applications, particularly in coordination chemistry and catalysis. This compound serves as an effective ligand, forming stable complexes with transition metals, which can be utilized in catalyzing chemical reactions, enhancing reaction rates, and improving selectivity in synthetic processes. Its ability to stabilize metal ions makes it valuable in the development of catalysts for organic synthesis, including cross-coupling reactions and oxidation processes.

In addition to its role in catalysis, Tris(2-benzimidazolylmethyl)amine is also explored in the fields of materials science and biochemistry. Its biocompatibility and potential for use in drug delivery systems highlight its relevance in pharmaceutical applications. Researchers appreciate its multifunctional nature, which allows for the design of innovative materials and therapeutic agents. With its robust performance and adaptability, Tris(2-benzimidazolylmethyl)amine stands out as a compound of choice for professionals seeking effective solutions in chemical synthesis and material development.

Numéro CAS 
64019-57-4
Formule moléculaire
C 24 H 21 N 7
Poids moléculaire 
407.48
Point de fusion 
277 - 281 °C (lit.)
Informations générales
Numéro CAS 
64019-57-4
Formule moléculaire
C 24 H 21 N 7
Poids moléculaire 
407.48
Point de fusion 
277 - 281 °C (lit.)
Propriétés
Informations complémentaires sur la propriété à venir prochainement !
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Sécurité et réglementation
Matières dangereuses
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Antibiotique
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Réglementé par la DEA
Non
Avertissements 
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Applications

Tris(2-benzimidazolylmethyl)amine is widely utilized in research focused on:

  • Catalysis: This compound serves as an effective ligand in various catalytic processes, enhancing reaction rates and selectivity in organic synthesis.
  • Coordination Chemistry: It forms stable complexes with transition metals, making it valuable in the development of new materials and in the study of metal-ligand interactions.
  • Biological Applications: Its unique structure allows it to interact with biological systems, potentially leading to the development of novel pharmaceuticals targeting specific enzymes or receptors.
  • Fluorescent Probes: The compound can be used to create fluorescent probes for biological imaging, aiding researchers in visualizing cellular processes in real-time.
  • Environmental Chemistry: It has applications in the removal of heavy metals from wastewater, showcasing its potential in environmental remediation efforts.

Citations