![(E)-10-(4-(5,5-dimethyl-1,3,2-dioxaborinan-2-yl)phenyl)-3-(4-(dimethylamino)styryl)-5,5-difluoro-1,7,9-trimethyl-5H-dipyrrolo[1,2-c:2',1'-f][1,3,2]diazaborinin-4-ium-5-uide](https://resource.bocsci.com/structure/949108-72-9.gif)
![(T-4)-[3-BRomo-5-[(4-bromo-3,5-dimethyl-2H-pyrrol-2-ylidene-κN)phenylmethyl]-2,4-dimethyl-1H-pyrrolato-κN]difluoroboron](/images/structure-default.jpg)
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3,5-distyryl-BODIPYs | CAS 1238620-18-2
| Catalog Number | F01-0128 |
| Category | BODIPY |
| Molecular Formula | C33H27BF2N |
| Molecular Weight | 486.392 |
* Please be kindly noted products are not for therapeutic use. We do not sell to patients.
Product Introduction
3,5-Distyryl-BODIPYs are a class of fluorescent dyes characterized by an extended conjugated system that enhances their photophysical properties. These compounds exhibit strong absorption and emission in the visible region, making them suitable for applications in fluorescence microscopy and bioimaging. Their structural features allow for efficient energy transfer processes, enabling their use as components in Förster Resonance Energy Transfer (FRET) assays.
Chemical Information
Product Specification
Application
Chemical Information
| Synonyms | Boron, difluoro[3-methyl-2-[[3-methyl-5-[(1E)-2-phenylethenyl]-2H-pyrrol-2-ylidene-κN]phenylmethyl]-5-[(1E)-2-phenylethenyl]-1H-pyrrolato-κN]-, (T-4)- |
Product Specification
| Excitation | 548 |
| Emission | 567 |
| Storage | Store at -20°C |
Application
3,5-distyryl-BODIPYs are fluorescent dyes with remarkable photophysical properties, making them highly valuable for various scientific and industrial applications. Here are some key applications of 3,5-distyryl-BODIPYs:
Biomedical Imaging: 3,5-distyryl-BODIPYs are extensively used in biomedical imaging due to their excellent fluorescence characteristics, such as high quantum yields and photostability. These dyes are ideal for labeling biomolecules, tissues, and cells, providing vivid contrasts in fluorescence microscopy. Their ability to track cellular events and interactions helps in understanding disease pathways and drug mechanisms.
Photodynamic Therapy (PDT): In cancer treatment, 3,5-distyryl-BODIPYs serve as photosensitizers in photodynamic therapy. When activated by light, these dyes generate reactive oxygen species that can destroy cancer cells. Their tunable wavelengths and minimal dark toxicity make them promising agents for non-invasive cancer therapies, offering targeted tumor ablation with reduced side effects.
Solar Energy: These compounds have shown great potential in solar energy applications, particularly in dye-sensitized solar cells (DSSCs). 3,5-distyryl-BODIPYs can efficiently harvest sunlight and convert it into electrical energy. Their highly tunable electronic properties and strong light absorption contribute to enhanced solar cell efficiencies and the development of renewable energy technologies.
Environmental Sensing: 3,5-distyryl-BODIPYs are employed as sensors for detecting environmental pollutants and chemical changes. Their sensitive fluorescence responses to various analytes, such as heavy metals and organic compounds, allow for real-time monitoring of environmental quality. This application is crucial for assessing ecosystem health and ensuring regulatory compliance.
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