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Catalog Number:
47553
CAS Number:
150321-92-9
7-méthoxycoumarine-3-carboxylate de N- succinimidyle
Purity:
≥ 98 % (HPLC)
Synonym(s):
Ester N -succinimidylique de l'acide 7-méthoxycoumarine-3-carboxylique
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$42.00 /0,1 G
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Informations sur le produit

N-Succinimidyl 7-methoxycoumarin-3-carboxylate is a versatile chemical compound widely utilized in bioconjugation and fluorescence applications. This compound features a unique structure that allows for efficient labeling of biomolecules, making it an essential tool for researchers in the fields of biochemistry and molecular biology. Its ability to form stable conjugates with proteins and nucleic acids enhances its utility in various assays, including fluorescence microscopy and flow cytometry. The methoxy group contributes to its photostability, ensuring reliable performance in experimental settings.

In addition to its labeling capabilities, N-Succinimidyl 7-methoxycoumarin-3-carboxylate is particularly advantageous for developing targeted drug delivery systems and studying protein interactions. Its high reactivity and specificity enable researchers to create precise conjugates, facilitating advanced studies in drug design and therapeutic applications. This compound stands out among similar reagents due to its excellent solubility and compatibility with a wide range of biological systems, making it a preferred choice for professionals seeking reliable and effective labeling solutions.

Numéro CAS 
150321-92-9
Formule moléculaire
C 15 H 117
Poids moléculaire 
317.25
Informations générales
Numéro CAS 
150321-92-9
Formule moléculaire
C 15 H 117
Poids moléculaire 
317.25
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

N-Succinimidyl 7-methoxycoumarin-3-carboxylate is widely utilized in research focused on:

  • Fluorescent Labeling: This compound is commonly used to label biomolecules, such as proteins and nucleic acids, allowing researchers to track and visualize these molecules in biological systems through fluorescence microscopy.
  • Drug Development: It plays a significant role in the pharmaceutical industry for the development of targeted drug delivery systems, enhancing the efficacy of therapeutic agents by improving their solubility and stability.
  • Bioconjugation: The compound is effective in bioconjugation processes, where it helps to attach various functional groups to biomolecules, facilitating the creation of complex biological probes for diagnostics.
  • Research in Cell Biology: It is utilized in cell biology studies to investigate cellular processes, such as protein interactions and localization, providing insights into cellular mechanisms and disease states.
  • Environmental Monitoring: This chemical can be applied in environmental science for the detection of pollutants, as its fluorescent properties allow for sensitive and selective analysis of contaminants in various samples.

Citations