
AF 555 azide
| Catalog Number | R01-0455 |
| Category | Alexa Fluor |
| Molecular Formula | C38H49K3N6O13S4 |
| Molecular Weight | 1043.38 |
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Product Introduction
AF 555 azide is a water-soluble, bright orange-fluorescent dye with excitation ideally suited for the 532 nm or 555 nm laser lines and visualized with TRITC (tetramethylrhodamine) filter sets.
Chemical Information
Product Specification
Application
Chemical Information
| IUPAC Name | tripotassium;(2Z)-2-[(E)-3-[1-[6-(3-azidopropylamino)-6-oxohexyl]-3,3-dimethyl-5-sulfonatoindol-1-ium-2-yl]prop-2-enylidene]-3-methyl-3-(4-sulfonatobutyl)-1-(3-sulfonatopropyl)indole-5-sulfonate |
| SMILES | CC1(C2=C(C=CC(=C2)S(=O)(=O)[O-])[N+](=C1C=CC=C3C(C4=C(N3CCCS(=O)(=O)[O-])C=CC(=C4)S(=O)(=O)[O-])(C)CCCCS(=O)(=O)[O-])CCCCCC(=O)NCCCN=[N+]=[N-])C.[K+].[K+].[K+] |
| InChI | InChI=1S/C38H52N6O13S4.3K/c1-37(2)30-26-28(60(52,53)54)15-17-32(30)43(22-7-4-5-14-36(45)40-20-10-21-41-42-39)34(37)12-9-13-35-38(3,19-6-8-24-58(46,47)48)31-27-29(61(55,56)57)16-18-33(31)44(35)23-11-25-59(49,50)51;;;/h9,12-13,15-18,26-27H,4-8,10-11,14,19-25H2,1-3H3,(H4-,40,45,46,47,48,49,50,51,52,53,54,55,56,57);;;/q;3*+1/p-3 |
| InChIKey | DAWUVPYNNYLDCF-UHFFFAOYSA-K |
| Appearance | Dark Red Solid |
Product Specification
| Excitation | 552 |
| Emission | 566 |
Application
AF 555 azide is a reactive azide-functionalized fluorescent labeling building block built around the AF 555 fluorophore, enabling copper-free click chemistry workflows for attaching bright red/orange emission tags to biomolecules and materials. Its azide handle is designed for strain-promoted azide-alkyne cycloaddition (SPAAC) and related click conjugation strategies, supporting efficient incorporation of a defined fluorophore into probes, conjugates, and surface coatings for fluorescence imaging and quantitative assays.
1. Biomolecule Labeling
AF 555 azide is commonly used by chemical biology and glycobiology groups to fluorescently label proteins, peptides, and other biomolecules via click conjugation to complementary cyclooctyne/alkyne partners. Researchers incorporate AF 555 into antibody conjugates, affinity reagents, and tracking probes where a stable, spectrally distinct fluorophore is required for multicolor fluorescence imaging and downstream quantitative readouts. The azide functionality supports modular probe construction, allowing the fluorophore to be introduced at the stage that best matches the biomolecule's handling constraints and purification workflow.
2. Fluorescence Microscopy Imaging
AF 555 azide is frequently selected for fluorescence microscopy experiments that benefit from a red/orange-emitting dye tag, including labeling of extracellular targets, cell-associated biomolecules, and engineered materials used as imaging scaffolds. In microscopy workflows, the click-ready azide enables researchers to prepare conjugates with controlled fluorophore loading and to swap targeting ligands or carriers while keeping the same imaging channel. This makes AF 555 azide practical for designing reproducible staining reagents for confocal imaging, widefield fluorescence microscopy, and immunofluorescence-style labeling schemes where click conjugation is preferred over less selective dye-attachment chemistries.
3. Flow Cytometry Staining
AF 555 azide supports fluorescence-based cell staining workflows where click conjugation is used to generate defined fluorescent conjugates for flow cytometry analysis. Lab teams use AF 555-containing labeling reagents to quantify cell-surface binding of tagged ligands, to monitor biomolecule uptake after conjugate preparation, and to build multicolor panels that include an AF 555 emission channel. The azide handle helps streamline reagent development by enabling consistent fluorophore installation onto targeting components, which is especially useful when comparing multiple ligands or conditions under standardized cytometry acquisition settings.
4. Surface Functionalization Coatings
AF 555 azide is also used in biomaterials and surface engineering to introduce fluorescent tags onto polymer surfaces, hydrogels, and other functional coatings through click-compatible immobilization strategies. Materials researchers employ AF 555 azide to visualize surface-bound ligands, characterize coating uniformity, and track biomolecule attachment on engineered substrates used in cell culture and material-matrix studies. By using the azide as a modular reactive group, teams can couple AF 555 to surface-presented cyclooctyne/alkyne functionalities and produce imaging-ready materials for microscopy and fluorescence-based quality control.
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