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4,4-Difluoro-8(4'-iodophenyl)-1,3,5,7-tetramethyl-4-bora-3a,4a-diaza-s-indacene | 250734-47-5
| Catalog Number | F01-0052 |
| Category | BODIPY |
| Molecular Formula | C19H18BF2IN2 |
| Molecular Weight | 450.078 |
| Catalog Number | Size | Price | Quantity |
|---|---|---|---|
| F01-0052 | -- | $-- |
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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.
Chemical Information |
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| Canonical SMILES | [B-]1(N2C(=CC(=C2C(=C3[N+]1=C(C=C3C)C)C4=CC=C(C=C4)I)C)C)(F)F |
| InChI | InChI=1S/C19H18BF2IN2/c1-11-9-13(3)24-18(11)17(15-5-7-16(23)8-6-15)19-12(2)10-14(4)25(19)20(24,21)22/h5-10H,1-4H3 |
| InChI Key | VPZZHCAOEMWMSI-UHFFFAOYSA-N |
- Product Specification
- Application
| Excitation | 503 |
| Emission | 509 |
| Storage | Store at -20°C |
The compound 4,4-Difluoro-8(4’-iodophenyl)-1,3,5,7-tetramethyl-4-bora-3a,4a-diaza-s-indacene, commonly referenced in scientific literature, plays a significant role in fluorescent research and finds diverse applications across biosciences.
Fluorescent Labeling in Biological Imaging: This compound, known for its exceptional fluorescence and photostability, is a go-to fluorescent marker in biological imaging. It can be linked to biomolecules like proteins and nucleic acids, enabling the visualization of intricate cellular processes using fluorescence microscopy. This crucial application aids in monitoring molecular interactions and dynamic changes within live cells, shedding light on the inner workings of biological systems.
Chemical Sensing: Employed in chemical sensors for its sensitivity to environmental cues that can modulate its fluorescence properties, this compound is integral in detecting ions, pH variations, and small molecules with remarkable specificity. These sensors play a vital role in environmental surveillance and biochemical analyses, offering precise monitoring capabilities for various applications.
Photodynamic Therapy Research: In the realm of photodynamic therapy investigations, this compound acts as a potent photosensitizer by generating reactive oxygen species upon exposure to light. Scientists are exploring its potential in targeting and eradicating cancerous cells, providing valuable insights into non-invasive strategies for combating cancer. This research avenue holds promise for advancing cancer treatment methodologies.
Advanced Material Science: Applied in the development of organic electronic materials such as organic light-emitting diodes (OLEDs), this compound’s unique properties make it a valuable component in creating materials with desirable optical attributes. Its role in enhancing the optical characteristics of materials is pivotal for driving advancements in optoelectronic devices and fostering innovations in material science.
Applications of Fluorescent Probes & Dyes
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