![(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-styryl-BODIPYs | CAS 1321616-68-5
| Catalog Number | F01-0121 |
| Category | BODIPY |
| Molecular Formula | C26H23BF2N2 |
| Molecular Weight | 412.29 |
* Please be kindly noted products are not for therapeutic use. We do not sell to patients.
Product Introduction
3-styryl-BODIPYs are a class of fluorescent dyes characterized by their extended conjugated aromatic systems, which enhance their photophysical properties. These compounds are known for their strong absorption and emission in the visible spectrum, making them suitable for various fluorescence imaging applications. The styryl modification allows for fine-tuning of their spectral properties, enabling their use as fluorogenic probes in bioimaging, where they can participate in energy transfer processes and serve as components in fluorescence resonance energy transfer (FRET) assays.
Product Specification
Application
Product Specification
| Excitation | 750 |
| Emission | 773 |
| Storage | Store at -20°C |
Application
3-styryl-BODIPYs, renowned for their exceptional photophysical properties, stand out as fluorescent dyes highly prized in diverse scientific realms. Here are four key applications of 3-styryl-BODIPYs intricately:
Fluorescence Imaging: Positioned at the forefront of fluorescence microscopy, 3-styryl-BODIPYs serve as indispensable tools for precise visualization of cellular components. Their vibrant fluorescence and remarkable light stability enable prolonged imaging sessions, rendering them ideal for tracing dynamic biological processes within living cells. Scientists frequently utilize these dyes to tag proteins, organelles, or cell membranes, facilitating in-depth structural analysis.
Biosensor Development: Essential in the realm of biosensor innovation, 3-styryl-BODIPYs play a pivotal role in the creation of biosensors tailored for detecting biological molecules or environmental shifts. Through the conjugation of 3-styryl-BODIPYs with specific biomolecules like antibodies or nucleic acids, researchers craft probes with remarkable sensitivity and selectivity. These biosensors find application across diverse sectors, encompassing medical diagnostics, environmental surveillance, and food safety assessments.
Photodynamic Therapy: At the cutting edge of cancer treatment modalities, 3-styryl-BODIPYs emerge as promising photosensitizers in photodynamic therapy (PDT). Upon illumination, these compounds unleash reactive oxygen species, triggering cell death selectively in targeted tumor cells. Their exceptional efficiency and specificity position them as standout contenders for minimally invasive cancer treatment strategies, heralding advances in oncological care.
Optoelectronic Devices: Embedded in the intricate web of optoelectronic innovation, 3-styryl-BODIPYs find application in the design of optoelectronic devices like organic light-emitting diodes (OLEDs) and solar cells. Their outstanding light absorption and emission characteristics contribute significantly to the advancement of high-performance, energy-efficient devices. Researchers persistently explore avenues for optimizing these dyes to elevate device efficiency and expand their technological footprint, driving the march towards enhanced device efficacy and broader application horizons.
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