
Cyanine3 alkyne
| Catalog Number | R02-0021 |
| Category | Alkynes |
| Molecular Formula | C33H40ClN3O |
| Molecular Weight | 530.14 |
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Product Introduction
Cyanine3 alkyne is a fluorophore ready for the use in Click Chemistry reaction.With this reagent, bright and photostable Cyanine3 reporter, an analog of Cy3®, can be attached to nearly any molecule bearing azide group.
Chemical Information
Product Specification
Application
Computed Properties
Chemical Information
| Related CAS | 1902918-31-3 (without anion) |
| Purity | NMR 1H (95%), HPLC-MS |
| IUPAC Name | 6-[3,3-dimethyl-2-[3-(1,3,3-trimethylindol-1-ium-2-yl)prop-2-enylidene]indol-1-yl]-N-prop-2-ynylhexanamide;chloride |
| SMILES | CC1(C2=CC=CC=C2[N+](=C1C=CC=C3C(C4=CC=CC=C4N3CCCCCC(=O)NCC#C)(C)C)C)C.[Cl-] |
| InChI | InChI=1S/C33H39N3O.ClH/c1-7-23-34-31(37)22-9-8-14-24-36-28-19-13-11-17-26(28)33(4,5)30(36)21-15-20-29-32(2,3)25-16-10-12-18-27(25)35(29)6;/h1,10-13,15-21H,8-9,14,22-24H2,2-6H3;1H |
| InChIKey | YIXIKYACJGHYQL-UHFFFAOYSA-N |
| Solubility | soluble in organic solvents (DMF, DMSO, dichloromethane), , practically insoluble in water (50 mg/L = 80 uM) |
| Appearance | red powder |
Product Specification
| ε, L⋅mol-1⋅cm-1 | 150000 |
| Fluorescence Quantum Yield | 0.31 |
| Excitation | 555 |
| Emission | 570 |
| Storage | 24 months after receival at -20°C in the dark. Transportation: at room temperature for up to 3 weeks. |
Application
Cyanine3 alkyne is a cyanine dye bearing a terminal alkyne handle, enabling copper(I)-catalyzed azide-alkyne cycloaddition (CuAAC) to install the fluorophore onto azide-functional biomolecules, targeting ligands, and polymer or surface materials. Its bright visible emission makes it a widely used fluorescent tag for constructing microscopy and flow cytometry labeling reagents, where the clickable alkyne provides a convenient way to generate dye conjugates with defined stoichiometry.
1. Biomolecule Click Labeling
Cyanine3 alkyne is used by chemical biology and glycobiology groups to fluorescently label azide-functional proteins, peptides, and carbohydrates via CuAAC, producing stable cyanine conjugates for binding and localization studies. Researchers frequently incorporate the dye into labeling workflows where a pre-functionalized biomolecule (azide-bearing) is available and a robust fluorescent readout is required for imaging, wash-based assays, or quantitative fluorescence measurements.
2. Fluorescent Probe Construction
Cyanine3 alkyne serves as a fluorophore building block for fluorescent probe development, especially when a modular design is needed to connect a cyanine reporter to a recognition element. Probe developers use the alkyne handle to couple Cyanine3 to azide-tagged scaffolds such as affinity ligands, nucleic-acid components, or engineered binding domains, enabling rapid generation of probe libraries for microscopy-based screening and fluorescence-based characterization of binding or interaction workflows.
3. Surface And Polymer Functionalization
Cyanine3 alkyne is applied in biomaterials research to create fluorescently labeled surfaces, coatings, and polymer conjugates by clicking the dye onto azide-functional materials. Materials scientists use the resulting cyanine-labeled constructs for tracking adsorption, monitoring surface interactions, and visualizing biomaterial interfaces under fluorescence microscopy, where the alkyne provides a practical route to incorporate a stable, visible fluorophore into otherwise non-fluorescent substrates.
4. Microscopy And Flow Cytometry Tagging
Cyanine3 alkyne supports fluorescence labeling strategies for cellular and molecular imaging workflows after click conjugation to azide-bearing targeting reagents. Imaging and cytometry users rely on the cyanine reporter to generate consistent fluorescent conjugates that can be used for microscopy visualization of labeled species and for flow cytometry readouts of fluorescently tagged biomolecules, including conjugates prepared from click-compatible ligands and carrier systems.
Computed Properties
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 3 |
| Rotatable Bond Count | 9 |
| Exact Mass | 529.2859906 g/mol |
| Monoisotopic Mass | 529.2859906 g/mol |
| Topological Polar Surface Area | 35.4Ų |
| Heavy Atom Count | 38 |
| Formal Charge | 0 |
| Complexity | 975 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 2 |
| Covalently-Bonded Unit Count | 2 |
| Compound Is Canonicalized | Yes |
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