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4,4-Difluoro-8-bithienyl-1,3,5,7-tetramethyl-BODIPY | CAS 1452398-18-3
| Catalog Number | F01-0057 |
| Category | BODIPY |
| Molecular Formula | C21H19BF2N2S2 |
| Molecular Weight | 412.335 |
* Please be kindly noted products are not for therapeutic use. We do not sell to patients.
Product Introduction
4,4-Difluoro-8-bithienyl-1,3,5,7-tetramethyl-BODIPY is a member of the BODIPY dye family, characterized by its boron-dipyrromethene core and extended bithienyl conjugation, which enhances its photophysical properties. This compound exhibits strong absorption and emission in the visible spectrum, making it suitable for fluorescence microscopy and flow cytometry applications. It features reactive sites that facilitate conjugation with biomolecules, enabling its use in the development of fluorescent probes for cellular imaging and biosensing assays.
Chemical Information
Product Specification
Application
Chemical Information
| Synonyms | 4,4-Difluoro-8-bithienyl-1,3,5,7-tetramethyl-4-bora-3a,4a-diaza-s-indacene |
Product Specification
| Excitation | 585 |
| Emission | 594 |
| Storage | Store at -20°C |
Application
4,4-Difluoro-8-bithienyl-1,3,5,7-tetramethyl-BODIPY is a fluorophore compound known for its impressive photophysical properties. Its applications span across several scientific and industrial fields. Here are some key applications of 4,4-Difluoro-8-bithienyl-1,3,5,7-tetramethyl-BODIPY:
Fluorescent Probing: In biochemical research, this BODIPY derivative is employed as a fluorescent probe for imaging and tracking biological molecules. Its high fluorescence quantum yield and stability make it ideal for labeling proteins, nucleic acids, and cell membranes. This application facilitates the visualization of cellular processes and molecular interactions in real-time.
Photodynamic Therapy: 4,4-Difluoro-8-bithienyl-1,3,5,7-tetramethyl-BODIPY is used in photodynamic therapy (PDT) for cancer treatment. As a photosensitizer, it generates reactive oxygen species upon light activation, inducing cell death in targeted cancer cells. This approach offers a minimally invasive alternative to traditional cancer treatments and is effective in targeting localized tumors.
Organic Electronics: This compound finds use in the development of organic electronic devices, including organic light-emitting diodes (OLEDs) and organic solar cells. Its strong absorption and emission properties contribute to the efficiency and performance of these devices. Researchers engineer materials that enhance optical and electronic characteristics, leading to innovations in display technology and renewable energy sources.
Environmental Sensing: 4,4-Difluoro-8-bithienyl-1,3,5,7-tetramethyl-BODIPY is employed in the design of chemical sensors for detecting environmental pollutants and hazardous substances. Its sensitivity to changes in the surrounding environment makes it effective for monitoring pH levels, metal ions, and toxic gases. This application aids in environmental protection and ensures safety in various industrial settings.
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