
Sulfo-Cyanine3 alkyne
| Catalog Number | R02-0031 |
| Category | Alkynes |
| Molecular Formula | C33H38KN3O7S2 |
| Molecular Weight | 691.90 |
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Product Introduction
Sulfo-Cyanine3 alkyne is a fluorescent probe featuring an alkyne functional group that participates in copper-catalyzed azide–alkyne cycloaddition reactions. This compound is commonly used in labeling chemistry, where its alkyne moiety enables conjugation to azide-functionalized biomolecules, facilitating the creation of stable triazole linkages. Its sulfo-Cyanine3 chromophore provides robust fluorescence properties, making it suitable for applications in imaging and tracking within complex biological systems.
Chemical Information
Product Specification
Application
Chemical Information
| Related CAS | 2055138-87-7 (inner salt) |
| Purity | NMR 1H, HPLC-MS (95%) |
| Solubility | soluble in water (0.57 M = 40 g/L), DMSO, DMF |
| Appearance | dark red powder |
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. |
Application
Sulfo-Cyanine3 alkyne is a sulfonated cyanine fluorophore bearing an alkyne handle, enabling copper-free click chemistry workflows for fluorescent labeling of biomolecules and materials. Its water-soluble, charged structure supports aqueous conjugation and downstream fluorescence imaging, while the cyanine dye provides strong visible-range signal for microscopy and flow-based readouts. Researchers use this reagent to build fluorescent conjugates where a stable dye tag and a click-compatible functional group are both required.
1. Biomolecule Fluorescent Labeling
Sulfo-Cyanine3 alkyne is commonly used by chemical biology and glycobiology groups to fluorescently label proteins, peptides, and other biomolecules through click-ready conjugation strategies. The sulfonated cyanine dye supports labeling in aqueous buffers, and the alkyne functionality allows incorporation of the fluorophore into larger constructs such as dye-tagged affinity reagents, tracking probes, and labeling standards. In practice, conjugates prepared from this reagent are frequently used to monitor binding, uptake, and localization in fluorescence microscopy experiments, as well as to verify labeling efficiency in fluorescence-based characterization workflows.
2. Flow Cytometry Dye Conjugates
Sulfo-Cyanine3 alkyne is used in flow cytometry workflows where a bright, water-compatible cyanine dye is needed for labeling cell-associated targets. By introducing the alkyne-bearing fluorophore into antibodies, ligands, or other targeting molecules via click chemistry, researchers generate fluorescent conjugates for analyzing binding to cell surfaces and for quantifying fluorescence intensity distributions across populations. The charged sulfonate group helps maintain aqueous handling during conjugate preparation and staining steps, supporting consistent staining and readout in standard flow cytometry instrument configurations.
3. Fluorescent Probe Construction
Sulfo-Cyanine3 alkyne serves as a practical building block for constructing fluorescent probes and imaging reagents that require a defined dye tag with a click-reactive handle. In probe development, the alkyne group is leveraged to assemble dye-containing conjugates for molecular imaging reagent libraries, including multicomponent labeling schemes where the cyanine signal is used as a reporter. This approach is widely adopted in assay development and microscopy studies that need modular fluorophore installation onto targeting scaffolds, polymer backbones, or biomaterial surfaces to visualize where and how labeled constructs localize during experiments.
4. Biomaterial And Surface Functionalization
Sulfo-Cyanine3 alkyne is also applied in biomaterials science to fluorescently functionalize hydrophilic surfaces and polymeric materials for imaging and material characterization. Researchers incorporate the dye into surface coatings or material conjugates using click-compatible assembly, enabling visualization of immobilized ligands, coating uniformity, and spatial distribution of functional groups. Such fluorescently modified materials are frequently used in microscopy-based studies of surface interactions, in platform development for labeled material assays, and in quality-control workflows that rely on direct fluorescence readout of surface-bound components.
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