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Catalog Number:
47752
CAS Number:
146616-66-2
Ester N- succinimidylique de l'acide 4,4-difluoro-5,7-diméthyl-4-bora-3 a ,4 a -diaza- s -indacène-3-propionique
Purity:
≥ 98 % (HPLC)
Synonym(s):
3-[3-[(2,5-dioxopyrrolidin-1-yl)oxy]-3-oxopropyl]-5,5-difluoro-7,9-diméthyl-5 H -dipyrrolo[1,2-c:2',1'-f][1,3,2]diazaborinin-4-ium-5-uide
Documents
$270.00 /5 mg
Taille
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Informations sur le produit

4,4-Difluoro-5,7-dimethyl-4-bora-3a,4a-diaza-s-indacene-3-propionic acid N-succinimidyl ester is a specialized chemical compound with significant applications in bioconjugation and fluorescent labeling. This compound is particularly valuable in the fields of biochemistry and molecular biology, where it serves as a reactive probe for labeling biomolecules such as proteins and nucleic acids. Its unique structure allows for efficient conjugation to amine-containing compounds, facilitating the development of targeted therapies and diagnostic tools.

The compound's fluorescence properties make it an excellent choice for applications in imaging and detection, providing researchers with the ability to visualize and track biological processes in real-time. Its stability and reactivity enhance its utility in various experimental setups, making it a preferred choice among professionals seeking reliable labeling reagents. With its potential to improve the sensitivity and specificity of assays, this compound is an essential tool for advancing research in cellular biology, drug development, and diagnostics.

Numéro CAS 
146616-66-2
Formule moléculaire
C18H18BF2N3O4
Poids moléculaire 
389.17
Point de fusion 
160 - 164 °C
Informations générales
Numéro CAS 
146616-66-2
Formule moléculaire
C18H18BF2N3O4
Poids moléculaire 
389.17
Point de fusion 
160 - 164 °C
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

4,4-Difluoro-5,7-dimethyl-4-bora-3a,4a-diaza-s-indacene-3-propionic acid N-succinimidyl ester is widely utilized in research focused on:

  • Fluorescent Labeling: This compound serves as a fluorescent probe in biological research, allowing scientists to tag proteins and other biomolecules for visualization under fluorescence microscopy.
  • Bioconjugation: It is used in the conjugation of biomolecules, such as antibodies or peptides, enhancing their stability and functionality for therapeutic applications.
  • Immunoassays: The compound is valuable in developing sensitive immunoassays, enabling the detection of low-abundance targets in complex biological samples.
  • Drug Development: Researchers utilize it in drug discovery processes to track and study the interactions of potential drug candidates with biological targets.
  • In Vivo Imaging: It plays a role in in vivo imaging studies, providing insights into biological processes and disease mechanisms through its fluorescent properties.

Citations