
Sulfo-Cyanine3 azide | CAS 1658416-54-6
| Catalog Number | F03-0002 |
| Category | sulfo-Cyanine3 |
| Molecular Formula | C33H41N6KO7S2 |
| Molecular Weight | 736.94 |
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Product Introduction
Sulfo-Cyanine3 azide is a water-soluble dye azide for Click Chemistry. Absorbance and emission of the dye are identical to Cy3® fluorophore.Brightness and photostability of fluorophore, together with high water solubility, makes this reagent an ideal choice for Click chemistry labeling of various molecules in aqueous phase.Click reaction can be carried out in pure water without need to use organic co-solvent. The reagent is designed for the labeling of sensitive molecules such as proteins, and even intact biological objects.
Chemical Information
Product Specification
Application
Chemical Information
| Related CAS | 2055138-89-9 (sodium salt) |
| Purity | NMR 1H, HPLC-MS (95%) |
| Solubility | soluble in water (0.62 M = 46 g/L), DMF, DMSO |
| Appearance | dark red crystals |
Product Specification
| ε, L⋅mol-1⋅cm-1 | 162000 |
| Fluorescence Quantum Yield | 0.1 |
| Excitation | 548 |
| Emission | 563 |
| 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. Desiccate. |
Application
Sulfo-Cyanine3 azide is a sulfonated cyanine dye click reagent designed for fluorescent labeling workflows that require azide functionality for bioorthogonal conjugation. Its water-soluble, membrane-compatible cyanine fluorophore enables bright fluorescence tracking of biomolecules and materials after azide-based coupling, supporting imaging and assay development where aqueous handling and dye conjugation are important.
1. Biomolecule Labeling
Sulfo-Cyanine3 azide is used by chemical biology and proteomics groups to install a cyanine3 fluorophore onto biomolecules through azide-enabled click conjugation. Researchers commonly incorporate the dye into labeling strategies for proteins, peptides, and other macromolecules that will be visualized by fluorescence microscopy or quantified in fluorescence-based assays. The sulfonated dye format supports aqueous conjugation and downstream handling, making it practical for preparing fluorescent conjugates used in binding studies, localization experiments, and reagent development for molecular imaging workflows.
2. Fluorescent Probe Construction
Sulfo-Cyanine3 azide supports fluorescent probe development where an azide handle is required to assemble imaging reagents from modular components. In probe construction pipelines, teams use the azide dye as a fluorescent reporter that can be linked to targeting ligands, affinity reagents, or scaffold molecules to create conjugated probes for cellular and biochemical imaging experiments. The cyanine3 optical reporter is particularly useful in workflows that rely on visible-range fluorescence readouts, including microscopy-based localization and plate-based fluorescence measurements for monitoring labeled constructs.
3. Surface And Biomaterial Functionalization
Sulfo-Cyanine3 azide is applied in biomaterials science to fluorescently tag surfaces and functional polymers using azide-based coupling strategies. Materials researchers use the dye to generate fluorescently labeled coatings, hydrogels, and surface-modified platforms that can be tracked during material characterization, imaging of interface behavior, or visualization of immobilized biomolecule layers. The sulfonated cyanine format helps maintain dye performance in aqueous environments typical of surface modification and washing steps, enabling robust visualization of functionalized materials in microscopy and related fluorescence characterization workflows.
4. Cell Imaging Labeling Studies
Sulfo-Cyanine3 azide is employed in fluorescence imaging studies where researchers need a cyanine3 reporter introduced via click-compatible azide chemistry. Lab teams use the dye to prepare fluorescently labeled biomolecule conjugates that can be imaged to follow distribution, uptake, or association patterns in cell-based experiments. Its sulfonated nature supports aqueous labeling protocols and helps maintain practical handling during staining and washing, enabling reproducible fluorescence labeling for microscopy readouts in chemical biology and imaging laboratories.
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