
Coumarin 343 azide | CAS 1807503-82-7
| Catalog Number | F06-0001 |
| Category | Coumarin |
| Molecular Formula | C22H27N5O5 |
| Molecular Weight | 441.48 |
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Product Introduction
Coumarin 343 azide is a fluorescent dye characterized by its coumarin chromophore, which exhibits strong blue fluorescence upon excitation. The azide functional group in its structure allows for bioorthogonal conjugation through click chemistry, making it suitable for labeling biomolecules in complex biological environments. This compound is often utilized in fluorescence microscopy and biosensing applications where its spectral properties and conjugation capabilities are leveraged for precise molecular tracking and imaging.
Chemical Information
Product Specification
Application
Chemical Information
| Purity | NMR 1H (95%) TLC, functional testing |
| Solubility | Good in organic solvents (DCM, chloroform, DMF, DMSO, MeCN, alcohols), poor in water |
| Appearance | yellow powder |
Product Specification
| ε, L⋅mol-1⋅cm-1 | 39000 |
| Fluorescence Quantum Yield | 0.63 |
| Excitation | 437 |
| Emission | 477 |
| Storage | 24 months after receival at -20°C in the dark. Transportation: at room temperature for up to 3 weeks. Avoid prolonged exposure to light. |
Application
Coumarin 343 azide is a coumarin-based fluorescent azide designed for bioorthogonal click chemistry workflows, enabling efficient incorporation of a bright, UV-excitable fluorophore into biomolecules, linkers, and polymer or surface architectures. The azide handle supports strain-promoted or catalyst-assisted azide-alkyne conjugation strategies used in chemical biology, where fluorescent labeling, tracking, and probe construction are required with minimal perturbation to the labeled target. In typical imaging and assay development, Coumarin 343 azide is selected for its strong fluorescence output and convenient chemical reactivity through the azide functional group.
1. Biomolecule Click Labeling
Coumarin 343 azide is used to fluorescently label proteins, peptides, and other biomolecules during bioconjugation workflows that rely on azide-alkyne coupling. Researchers incorporate the dye into affinity reagents, labeling tags, and tracking conjugates to visualize binding, uptake, or distribution in microscopy-based studies, while keeping the fluorophore chemically addressable through the azide functionality. This approach is common in chemical biology laboratories building fluorescent conjugates for mechanistic studies, imaging reagent optimization, and assay development where a coumarin fluorophore provides strong signal under UV excitation.
2. Fluorescence Microscopy Tracing
Coumarin 343 azide supports cellular and biomaterial fluorescence microscopy applications where fluorescent tracking of labeled components is required. By clicking the azide dye onto alkyne-functional targets such as biomolecule conjugates, cell-surface engineered handles, or polymeric materials, investigators generate imaging reagents that report the spatial localization of the modified species. Coumarin 343 azide is frequently selected for experiments that benefit from a bright coumarin emission profile and straightforward conjugation into complex biological or materials systems, including co-localization studies with other fluorescent markers and time-course imaging of labeled constructs.
3. Polymer And Surface Functionalization
Coumarin 343 azide is also used in materials science and industrial R&D to create fluorescently functional polymers, hydrogels, and engineered surfaces via click chemistry. Incorporation of the azide fluorophore into alkyne-bearing matrices enables preparation of labeled coatings, diffusion-tracking materials, and fluorescence-tagged biomaterials used to monitor transport, distribution, or surface association. This application is particularly relevant for researchers who need a chemically stable fluorescent tag that can be introduced through a defined reactive handle, producing reproducible labeling of macromolecular or surface platforms for characterization and process development.
4. Fluorescent Probe Construction
Coumarin 343 azide is frequently employed as a fluorophore building block for constructing fluorescent probes and labeling reagents in chemical biology. The azide group allows coupling to probe scaffolds, linkers, and recognition constructs that are subsequently used for fluorescence readouts in imaging and plate-based assays. Teams developing molecular imaging reagents use Coumarin 343 azide to generate fluorescent conjugates with defined attachment points, enabling controlled probe assembly for studies of binding events, reagent localization, and fluorescent reporting of engineered chemical structures.
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