1,3,5,7-Tetramethyl-8-(C3-COOH)4,4-difluoro-4-bora-3a,4a-diaza-s-indacene | CAS 878674-84-1

Catalog Number	F01-0117
Category	BODIPY
Molecular Formula	C17H21BF2N2O2
Molecular Weight	334.17

Catalog Number	Size	Price	Quantity
F01-0117	10 mg	$298

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Product Introduction

BODIPY dyes are used to generate fluorescent conjugates of proteins, nucleotides, oligonucleotides and dextrans, as well as to prepare fluorescent enzyme substrates, fatty acids, phospholipids, lipopolysaccharides, receptor ligands and polystyrene microspheres.

Chemical Information
Product Specification
Application

Synonyms	4-(4,4-Difluoro-1,3,5,7-tetramethyl-4-bora-3a,4a-diaza-s-indacene-8-yl)-butyric Acid
Purity	98%
Appearance	Orange solid

Excitation	646
Emission	662
Storage	Store at -20°C

1,3,5,7-Tetramethyl-8-(C3-COOH)-4,4-difluoro-4-bora-3a,4a-diaza-s-indacene, known as a BODIPY derivative, is a versatile fluorescent dye widely utilized in scientific research. Here are four key applications:

Fluorescence Imaging: This BODIPY derivative plays a pivotal role in fluorescence imaging, allowing researchers to fluorescently tag and visualize biological molecules within cellular environments. Its exceptional photostability and brightness make it an ideal choice for conducting extended imaging studies. Scientists leverage this dye to monitor intricate cellular processes, such as protein localization and dynamic activities in real-time, providing valuable insights into cellular behavior and interactions.

Molecular Probes: Serving as a valuable molecular probe, this compound facilitates the exploration of diverse biochemical interactions and pathways. With its remarkable fluorescence properties, it can be conjugated with biomolecules like nucleic acids and proteins to track their activities and interactions. This aids in unraveling complex cellular mechanisms and identifying potential targets for therapeutic interventions, offering a deeper understanding of cellular dynamics and signaling pathways.

Energy Transfer Studies: BODIPY derivatives, including this specific compound, are integral to conducting Förster Resonance Energy Transfer (FRET) studies, allowing researchers to delve into molecular interactions. By acting as a donor or acceptor in FRET experiments, this compound enables scientists to quantify the proximity and interactions between two fluorescently-labeled molecules. This technique yields valuable insights into molecular binding events and conformational changes, shedding light on intricate molecular relationships and structural alterations.

Chemical Sensing: This fluorescent dye also finds application in the development of cutting-edge chemical sensors, facilitating the detection of specific ions, molecules, or environmental changes through fluorescence signal variations. Integration of this dye into sensor platforms enables researchers to monitor environmental conditions, diagnose medical issues, and optimize industrial processes. These sensors offer a versatile solution for diverse applications, ranging from environmental monitoring to healthcare diagnostics and industrial quality control.