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Catalog Number:
23111
CAS Number:
91990-88-4
4-(N-Succinimidylcarboxy)benzophenone
Purity:
≥ 99% (NMR)
Synonym(s):
4-Benzoylbenzoic acid succinimidyl ester
Documents
$93.14 /25MG
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Product Information

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.

Synonyms
4-Benzoylbenzoic acid succinimidyl ester
CAS Number
91990-88-4
Purity
≥ 99% (NMR)
Molecular Formula
C18H13NO5
Molecular Weight
323.3
MDL Number
MFCD00058572
PubChem ID
2762595
Melting Point
203-208 °C
Appearance
White solid
Conditions
Store at 0-8 °C
General Information
Synonyms
4-Benzoylbenzoic acid succinimidyl ester
CAS Number
91990-88-4
Purity
≥ 99% (NMR)
Molecular Formula
C18H13NO5
Molecular Weight
323.3
MDL Number
MFCD00058572
PubChem ID
2762595
Melting Point
203-208 °C
Appearance
White solid
Conditions
Store at 0-8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
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