2,6-Diiodo-1,3,5,7-tetramethyl-8-(4-iodophenyl)-4,4-difluoroboradiazasindacene

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2,6-Diiodo-1,3,5,7-tetramethyl-8-(4-iodophenyl)-4,4-difluoroboradiazasindacene

2,6-Diiodo-1,3,5,7-tetramethyl-8-(4-iodophenyl)-4,4-difluoroboradiazasindacene | 1031443-56-7

Catalog Number F01-0081
Category BODIPY
Molecular Formula C19H16BF2I3N2
Molecular Weight 701.871
Catalog Number Size Price Quantity
F01-0081 -- $--

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 646
Emission 662
Storage Store at -20°C

2,6-Diiodo-1,3,5,7-tetramethyl-8-(4-iodophenyl)-4,4-difluoroboradiazasindacene, commonly referred to as a BODIPY derivative, is a fluorescent compound highly sought after in scientific research due to its versatile range of applications.

Fluorescent Probes: Renowned for its outstanding fluorescence properties, this BODIPY compound serves as a coveted probe in various imaging techniques. Emitting robust fluorescence with a high quantum yield, it is utilized to label biomolecules in studies of cellular and molecular biology. Researchers deploy this compound to trace cellular processes, visualize cell compartments, and investigate protein interactions within live cells with unparalleled precision.

Photodynamic Therapy: Within the realm of cancer therapy, BODIPY derivatives are being investigated as potential photosensitizers in photodynamic therapy (PDT). When exposed to specific light wavelengths, this compound initiates the generation of reactive oxygen species capable of eradicating cancer cells. Its adaptable photophysical characteristics position it as a prospect for targeted cancer treatment, offering a minimally invasive therapeutic avenue with remarkable potential.

Sensory Applications: BODIPY derivatives play a vital role in the advancement of chemical sensors for detecting ions, pH fluctuations, and other environmental changes. Through structural modifications, researchers craft sensors with tailored binding affinities and fluorescence alterations in response to desired analytes. This capability is essential for real-time surveillance of environmental parameters and biological processes, facilitating enhanced understanding of dynamic events.

Organic Electronics: In the domain of materials science, BODIPY compounds contribute to the evolution of organic electronic devices like organic light-emitting diodes (OLEDs) and solar cells. Their pronounced absorption and emission properties, coupled with robust thermal and photostability, enhance their efficacy in these applications. Scientists strive to optimize these materials to elevate device efficiency and performance, propelling the frontier of organic electronics forward.

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