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Catalog Number:
47553
CAS Number:
150321-92-9
N -succinimidilo 7-metoxicumarina-3-carboxilato
Purity:
≥ 98 % (HPLC)
Synonym(s):
Éster N -succinimidílico del ácido 7-metoxicumarina-3-carboxílico
Documents
$42.00 /0,1 g
Tamaño
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Product Information

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.

Synonyms
Éster N -succinimidílico del ácido 7-metoxicumarina-3-carboxílico
CAS Number
150321-92-9
Purity
≥ 98 % (HPLC)
Molecular Formula
C 15 H 11 N.º 7
Molecular Weight
317.25
MDL Number
MFCD00467593
PubChem ID
2760554
Appearance
Polvo casi blanco
Conditions
Conservar a < -10 °C, bajo gas inerte.
General Information
Synonyms
Éster N -succinimidílico del ácido 7-metoxicumarina-3-carboxílico
CAS Number
150321-92-9
Purity
≥ 98 % (HPLC)
Molecular Formula
C 15 H 11 N.º 7
Molecular Weight
317.25
MDL Number
MFCD00467593
PubChem ID
2760554
Appearance
Polvo casi blanco
Conditions
Conservar a < -10 °C, bajo gas inerte.
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
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.

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