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Catalog Number:
23111
CAS Number:
91990-88-4
4-( N -Succinimidylcarboxy)benzophénone
Purity:
≥ 99% (RMN)
Synonym(s):
Ester succinimidylique de l'acide 4-benzoylbenzoïque
Documents
$93.14 /25 mg
Taille
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Informations sur le produit

4-(N-Succinimidylcarboxy)benzophenone is a versatile chemical compound widely utilized in bioconjugation and labeling applications. This compound features a succinimidyl ester group, which enhances its reactivity with amines, making it an ideal choice for the development of targeted drug delivery systems and biomolecular probes. Researchers often employ this compound in the synthesis of fluorescent labels and affinity reagents, facilitating the study of protein interactions and cellular processes. Its ability to form stable conjugates with biomolecules allows for precise tracking and analysis in various biological assays.

Additionally, 4-(N-Succinimidylcarboxy)benzophenone is recognized for its unique photophysical properties, which contribute to its effectiveness in imaging applications. Its stability under physiological conditions and compatibility with a range of substrates make it a preferred choice for researchers in the fields of biochemistry and molecular biology. By incorporating this compound into their workflows, professionals can enhance the specificity and sensitivity of their experiments, ultimately leading to more reliable and reproducible results.

Numéro CAS 
91990-88-4
Formule moléculaire
C 18 H 135
Poids moléculaire 
323.3
Point de fusion 
203-208 °C
Informations générales
Numéro CAS 
91990-88-4
Formule moléculaire
C 18 H 135
Poids moléculaire 
323.3
Point de fusion 
203-208 °C
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

4-(N-Succinimidylcarboxy)benzophenone is widely utilized in research focused on:

  • Bioconjugation: This compound serves as a versatile linker in the bioconjugation of proteins and antibodies, allowing for the development of targeted therapeutics and diagnostics.
  • Fluorescent Labeling: It is used in the labeling of biomolecules for fluorescence microscopy, enhancing visualization in cellular studies and providing insights into biological processes.
  • Drug Delivery Systems: The compound plays a crucial role in the design of drug delivery systems, improving the efficacy and specificity of therapeutic agents in cancer treatment.
  • Surface Modification: It is applied in modifying surfaces of materials to improve biocompatibility, which is essential in medical device manufacturing and tissue engineering.
  • Research in Chemical Biology: This chemical is instrumental in studying protein interactions and dynamics, contributing to advancements in understanding cellular mechanisms and disease pathways.

Citations