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Catalog Number:
23034
CAS Number:
92944-71-3
4-(N-Maleimido)benzophenone
Purity:
≥ 98% (HPLC)
Synonym(s):
1-(4-Benzoylphenyl)-1H-pyrrole-2,5-dione
Documents
$105.56 /100MG
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Product Information

4-(N-Maleimido)benzophenone is a versatile compound widely utilized in the fields of organic chemistry and materials science. This compound serves as an effective photoinitiator in UV-curable coatings and adhesives, enabling rapid curing processes that enhance production efficiency. Its unique maleimide functionality allows for selective reactions with thiols, making it invaluable in the development of bioconjugates and drug delivery systems. Researchers appreciate its stability under UV light and its ability to facilitate cross-linking in polymer matrices, which is crucial for creating durable materials with tailored properties.

In addition to its applications in coatings and adhesives, 4-(N-Maleimido)benzophenone is also employed in the synthesis of advanced materials, including hydrogels and nanocomposites. Its ability to form covalent bonds with various substrates opens up possibilities for innovative applications in biomedical devices and sensors. The compound's efficiency and effectiveness in promoting chemical reactions make it a preferred choice for professionals seeking reliable solutions in their research and industrial applications.

Synonyms
1-(4-Benzoylphenyl)-1H-pyrrole-2,5-dione
CAS Number
92944-71-3
Purity
≥ 98% (HPLC)
Molecular Formula
C17H11NO3
Molecular Weight
277.28
MDL Number
MFCD00079465
PubChem ID
146390
Melting Point
155 - 157 ?C
Appearance
Light yellow solid powder
Conditions
Store at 0-8°C
General Information
Synonyms
1-(4-Benzoylphenyl)-1H-pyrrole-2,5-dione
CAS Number
92944-71-3
Purity
≥ 98% (HPLC)
Molecular Formula
C17H11NO3
Molecular Weight
277.28
MDL Number
MFCD00079465
PubChem ID
146390
Melting Point
155 - 157 ?C
Appearance
Light yellow solid powder
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-Maleimido)benzophenone is widely utilized in research focused on:

  • Chemical Synthesis: This compound serves as a versatile reagent in the synthesis of various polymers and bioconjugates, enhancing the development of advanced materials.
  • Photoinitiators: It is commonly used in UV-curable coatings and adhesives, where it acts as a photoinitiator, enabling rapid curing processes that improve production efficiency.
  • Bioconjugation: Researchers leverage its maleimide group for selective conjugation to thiol-containing biomolecules, facilitating the creation of targeted drug delivery systems and diagnostic tools.
  • Fluorescent Probes: The compound can be employed in the design of fluorescent probes for biological imaging, providing insights into cellular processes and disease mechanisms.
  • Material Science: It plays a role in the development of functionalized surfaces and nanomaterials, contributing to innovations in electronics and sensor technologies.

Citations