2,6-Diiodo-1,3,5,7,8-pentaethyl-BODIPY

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2,6-Diiodo-1,3,5,7,8-pentaethyl-BODIPY

2,6-Diiodo-1,3,5,7,8-pentaethyl-BODIPY | 1031443-55-6

Catalog Number F01-0074
Category BODIPY
Molecular Formula C14H15BF2I2N2
Molecular Weight 513.90
Catalog Number Size Price Quantity
F01-0074 50 mg $399
F01-0074 100 mg $499

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 nm
Emission 662 nm
Storage Store at -20°C

2,6-Diiodo-1,3,5,7,8-pentaethyl-BODIPY is a fluorescent dye known for its exceptional photostability and bright fluorescence, making it ideal for various scientific applications.

Biotechnological Assays: This BODIPY dye is extensively used in biotechnological assays due to its strong fluorescence and ability to label biomolecules. Researchers employ it in flow cytometry to analyze cell populations by staining cells with fluorescently tagged antibodies. It is also used in fluorescence microscopy for tracking cell structures and dynamics, providing clear imaging of biological samples.

Photodynamic Therapy: 2,6-Diiodo-1,3,5,7,8-pentaethyl-BODIPY is applied in photodynamic therapy (PDT) for its capacity to generate reactive oxygen species when exposed to light. In PDT, it is used to treat certain types of cancers and infections by inducing cell death in targeted areas. Its iodine substitution enhances its efficacy as a photosensitizer, offering potential benefits in developing advanced therapeutic interventions.

Environmental Monitoring: The dye is also valuable in environmental science for tracking pollutants and studying ecological processes. By labeling specific environmental samples or organisms, it allows for the visualization and monitoring of pollutant distribution and uptake. This assists in understanding the impact of pollutants on ecosystems and devising strategies for environmental management and protection.

Chemical Sensing: 2,6-Diiodo-1,3,5,7,8-pentaethyl-BODIPY is used in the creation of chemical sensors due to its sensitivity and selectivity for various analytes. It serves as a probe for detecting changes in environmental conditions such as pH, metal ion concentration, and molecular interactions. These sensors are applied in both scientific research and industrial quality control, providing critical data for various fields.

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