
1,7-Dimethyl-3,5-bis(phenylethenyl)-8-(4-iodophenyl)-4,4-difluoboradiazasindacene | 1256917-88-0
Catalog Number | F01-0133 |
Category | BODIPY |
Molecular Formula | C53H34BF2IN2 |
Molecular Weight | 874.579 |
Catalog Number | Size | Price | Quantity |
---|---|---|---|
F01-0133 | -- | $-- |
* 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 | 648 |
Emission | 671 |
Storage | Store at -20°C |
1,7-Dimethyl-3,5-bis(phenylethenyl)-8-(4-iodophenyl)-4,4-difluoboradiazasindacene, a fluorescent dye renowned for its advanced photophysical characteristics, finds diverse applications across various fields.
Fluorescence Imaging: Widely employed in biological and medical imaging, this compound's intense fluorescence properties render it indispensable for tracking and visualizing biological processes with exceptional sensitivity. Its bright and stable fluorescence is particularly advantageous for long-term studies and live-cell imaging, providing researchers with a powerful tool for exploring the intricacies of cellular behavior.
Cancer Diagnostics: In the realm of oncology, this compound plays a crucial role in diagnostic assays for detecting cancerous cells. Its strong fluorescence acts as a distinguishing marker that can bind to specific cancer cell receptors, enhancing the contrast in imaging modalities like flow cytometry and confocal microscopy. By enabling accurate identification and quantification of cancer cells, this compound supports early diagnosis and monitoring of treatment efficacy.
Chemical Sensing: Utilized in the development of chemical sensors, this compound exhibits the ability to detect ions and small molecules through fluorescence response to binding events. Its sensitivity as a probe makes it invaluable for detecting chemical species such as metal ions and environmental pollutants, with implications for environmental monitoring and industrial applications that rely on precise chemical detection mechanisms.
Material Science: Within the realm of materials science, this dye is harnessed to manipulate and elevate the optical properties of materials. By integrating it into polymers and nanomaterials, researchers can fashion luminescent materials essential for photonics and optoelectronics applications. These advancements drive innovation in technologies like display systems and light-emitting devices, showcasing the multifaceted utility of this compound in material engineering.
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