1,3,5,7-tetramethyl-2,6-diiodo-C3-SE-BODIPYs | CAS 1825368-13-5

Catalog Number	F01-0119
Category	BODIPY
Molecular Formula	C21H22BF2I2N3O4
Molecular Weight	683.04

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Product Introduction

Heavy-atom BODIPY derivative designed for singlet oxygen generation. Perfect for photodynamic therapy and optical sensing.

Product Specification
Application

Storage

Store at -20°C

1,3,5,7-tetramethyl-2,6-diiodo-C3-SE-BODIPYs fluorescent dyes with exceptional characteristics find diverse applications in scientific fields.

Bioimaging: In the realm of bioimaging, researchers rely on the exceptional fluorescence and photostability of these BODIPY derivatives for visualizing and monitoring cellular processes. Their capacity to traverse cell membranes facilitates high-resolution imaging of live cells across diverse experimental scenarios, ideal for exploring dynamic biological phenomena and cellular localization in both research and medical diagnostics.

Photodynamic Therapy: Delving into the domain of photodynamic therapy (PDT), these specialized compounds serve as potent photosensitizers, generating reactive oxygen species post-light activation. Selectively targeting and annihilating cancerous cells, they present an attractive non-invasive treatment avenue. Their precision and effectiveness in inducing cell demise position them as promising contenders in the realm of cancer therapy, offering hope for improved patient outcomes.

Sensors and Probes: Functioning as versatile sensors and probes, these BODIPY compounds exhibit tunable fluorescence properties conducive to detecting specific ions or molecules. By responding to environmental shifts like pH or ion concentration through alterations in fluorescence intensity or wavelength, they play a pivotal role in crafting sensitive diagnostic instruments and environmental monitoring devices, crucial for advancing scientific research and environmental protection efforts.

Energy Transfer Studies: Engaging in energy transfer studies, 1,3,5,7-tetramethyl-2,6-diiodo-C3-SE-BODIPYs act as key players in Förster Resonance Energy Transfer (FRET) experiments, functioning as either acceptors or donors. Their spectral attributes enable seamless participation in energy transfer processes, facilitating exploration of molecular interactions and distances. This application proves invaluable for probing intricate processes such as protein folding, conformational changes, and interactions within complex biological systems.