
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 | |
F01-0074 | -- | -- |
* Please be kindly noted products are not for therapeutic use. We do not sell to patients.
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.
Recommended Services
Blogs & Technical Articles

- Hoechst Dyes: Definition, Structure, Mechanism and Applications
- Mastering the Spectrum: A Comprehensive Guide to Cy3 and Cy5 Dyes
- Fluorescent Probes: Definition, Structure, Types and Application
- Fluorescent Dyes: Definition, Mechanism, Types and Application
- Coumarin Dyes: Definition, Structure, Benefits, Synthesis and Uses
- BODIPY Dyes: Definition, Structure, Synthesis and Uses
- Cyanine Dyes: Definition, Structure, Types and Uses
- Fluorescein Dyes: Definition, Structure, Synthesis and Uses
- Rhodamine Dyes: Definition, Structure, Uses, Excitation and Emission
- Unlocking the Power of Fluorescence Imaging: A Comprehensive Guide
- Cell Imaging: Definitions, Systems, Protocols, Dyes, and Applications
- Lipid Staining: Definition, Principles, Methods, Dyes, and Uses
- Flow Cytometry: Definition, Principles, Protocols, Dyes, and Uses
- Nucleic Acid Staining: Definition, Principles, Dyes, Procedures, and Uses
- DNA Staining: Definition, Procedures, Benefits, Dyes and Uses
- Cell Staining: Definition, Principles, Protocols, Dyes, and Uses
- Ion Imaging: Definition, Principles, Benefits, Dyes, and Uses
- Fluorescent Labeling: Definition, Principles, Types and Applications
Recommended Products