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Catalog Number:
23000
CAS Number:
42189-56-0
N-(1-Pyrenyl)maleimide
Purity:
≥ 98% (HPLC)
Synonym(s):
1-(1-Pyrenyl)-1H-pyrrole-2,5-dione
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$65.40 /250MG
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Product Information

N-(1-Pyrenyl)maleimide is a versatile compound widely recognized for its unique fluorescent properties, making it an excellent choice for applications in materials science and biochemistry. This compound serves as a valuable fluorescent probe in various research settings, particularly in the study of protein interactions and cellular imaging. Its ability to form stable conjugates with biomolecules allows researchers to track and visualize biological processes in real-time, enhancing our understanding of cellular dynamics. Additionally, N-(1-Pyrenyl)maleimide is utilized in the development of advanced materials, such as polymers and nanocomposites, where its fluorescence can be harnessed for sensing applications or as a marker in diagnostic tools.

The compound's distinctive pyrene moiety contributes to its strong photophysical properties, making it a preferred choice for researchers seeking reliable fluorescent markers. Its compatibility with various solvents and ease of incorporation into different matrices further enhance its utility in both academic and industrial settings. Whether in the realm of drug discovery, environmental monitoring, or the development of innovative materials, N-(1-Pyrenyl)maleimide stands out as a powerful tool that can significantly advance research and application outcomes.

Synonyms
1-(1-Pyrenyl)-1H-pyrrole-2,5-dione
CAS Number
42189-56-0
Purity
≥ 98% (HPLC)
Molecular Formula
C20H11NO2
Molecular Weight
297.32
MDL Number
MFCD00049301
PubChem ID
626783
Melting Point
235-237 °C
Appearance
Green solid powder
Conditions
Store at 0-8 °C
General Information
Synonyms
1-(1-Pyrenyl)-1H-pyrrole-2,5-dione
CAS Number
42189-56-0
Purity
≥ 98% (HPLC)
Molecular Formula
C20H11NO2
Molecular Weight
297.32
MDL Number
MFCD00049301
PubChem ID
626783
Melting Point
235-237 °C
Appearance
Green 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

N-(1-Pyrenyl)maleimide is widely utilized in research focused on:

  • Fluorescent Probes: This compound serves as a fluorescent label in biological research, allowing scientists to track cellular processes and interactions with high sensitivity.
  • Polymer Chemistry: It is used in the synthesis of functionalized polymers, enhancing their properties for applications in coatings and materials science.
  • Bioconjugation: The compound is effective in attaching biomolecules to surfaces, which is crucial for developing biosensors and diagnostic tools.
  • Photophysics Studies: Researchers utilize it to study energy transfer and photophysical properties, contributing to advancements in photonic devices.
  • Drug Delivery Systems: Its unique properties enable the design of targeted drug delivery systems, improving therapeutic efficacy and reducing side effects.

Citations