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BODIPY
1,5,7-Trimethyl-3-(E-4-hydroxyphenylethenyl)-8-phenyl-4,4-difluoroboradiazasindacene

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1,5,7-Trimethyl-3-(E-4-hydroxyphenylethenyl)-8-phenyl-4,4-difluoroboradiazasindacene

1,5,7-Trimethyl-3-(E-4-hydroxyphenylethenyl)-8-phenyl-4,4-difluoroboradiazasindacene | CAS 1373612-56-6

Catalog Number	F01-0062
Category	BODIPY
Molecular Formula	C26H23BF2N2O
Molecular Weight	428.289

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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.

Product Specification
Application

Excitation	565
Emission	574
Storage	Store at -20°C

1,5,7-Trimethyl-3-(E-4-hydroxyphenylethenyl)-8-phenyl-4,4-difluoroboradiazasindacene, a BODIPY derivative, is a fluorescent compound featuring an extended π-conjugation through a hydroxyphenylethenyl group and additional methyl and phenyl substitutions. This structural modification enhances its optical properties, including high fluorescence quantum yield, photostability, and tunable absorption/emission spectra, making it a highly versatile dye for various scientific and industrial applications.

This compound is widely used in fluorescence imaging and microscopy due to its strong emission intensity and stability. It is particularly suited for tracking biological processes, visualizing cellular structures, and monitoring molecular interactions in real time, contributing significantly to advancements in cell biology and medical diagnostics.

1,5,7-Trimethyl-3-(E-4-hydroxyphenylethenyl)-8-phenyl-BODIPY is a key player in chemical sensing applications. Its hydroxyphenylethenyl group enhances sensitivity to environmental changes, allowing the dye to act as a selective probe for detecting analytes like ions, reactive oxygen species (ROS), and biomolecules in environmental and biomedical contexts.

The compound finds use in photodynamic therapy (PDT) as a photosensitizer. Upon light activation, it efficiently produces singlet oxygen and other reactive species, enabling its application in targeted cancer treatment and antimicrobial therapies, combining therapeutic action with potential fluorescence-guided diagnostics.

In material science, this BODIPY derivative is employed in the development of optoelectronic devices, including organic light-emitting diodes (OLEDs) and dye-sensitized solar cells. Its extended conjugation and photophysical properties contribute to high energy conversion efficiency and stability, making it an essential material for next-generation technologies.