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BODIPY
2,6-Diiodo-1,5,7-trimethyl-3-(4-propargyloxyphenylethenyl)-8-phenyl-4,4-difluoroboradiazasindacene

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2,6-Diiodo-1,5,7-trimethyl-3-(4-propargyloxyphenylethenyl)-8-phenyl-4,4-difluoroboradiazasindacene

2,6-Diiodo-1,5,7-trimethyl-3-(4-propargyloxyphenylethenyl)-8-phenyl-4,4-difluoroboradiazasindacene | CAS 1632007-42-1

Catalog Number	F01-0080
Category	BODIPY
Molecular Formula	C29H23BF2I2N2O
Molecular Weight	718.131

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* Please be kindly noted products are not for therapeutic use. We do not sell to patients.

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Product Introduction

Click-ready iodo-BODIPY with extended conjugation for red emission. Ideal for bioconjugation and ratiometric sensor construction.

Product Specification
Application

Excitation	649
Emission	667
Storage	Store at -20°C

2,6-Diiodo-1,5,7-trimethyl-3-(4-propargyloxyphenylethenyl)-8-phenyl-4,4-difluoroboradiazasindacene is a fluorescent dye with promising applications in the field of biochemical research.

Fluorescence Microscopy: This compound can be used as a fluorescent probe in microscopy to visualize cellular structures and molecular interactions. Its unique spectral properties allow for high-resolution imaging of live cells, providing insights into cellular dynamics. Researchers can employ this dye in multicolor fluorescence microscopy to study complex biological processes.

Fluorescent Tagging in Molecular Biology: The compound serves as an excellent fluorescent tag for biomolecules such as proteins, nucleic acids, and other small molecules. By tagging these biomolecules, scientists can track their localization and movement within cells. This is crucial for understanding molecular pathways and interactions within cellular environments.

Biolabeling and Biosensing: In biosensing applications, this fluorescent compound can be used to detect specific biomolecules in complex biological samples. When conjugated with biomolecular recognition elements, it acts as a sensitive reporter in assays for detecting proteins, nucleic acids, or other analytes. Such applications are vital for diagnostics and monitoring biochemical changes in real-time.

Photodynamic Therapy Research: The compound's ability to generate reactive oxygen species upon light activation makes it a candidate for photodynamic therapy (PDT) research. Researchers can explore its potential as a photosensitizer to target and kill cancer cells. This approach combines the compound's imaging capabilities with therapeutic functions, offering dual benefits in cancer treatment studies.