
AF 568 azide
| Catalog Number | R01-0459 |
| Category | Alexa Fluor |
| Molecular Formula | C36H34K2N6O10S2 |
| Molecular Weight | 853.02 |
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Product Introduction
AF 568 is a fluorescent dye with excitation peak at 572 nm and emission peak at 598 nm.
Chemical Information
Product Specification
Application
Chemical Information
| IUPAC Name | dipotassium;[13-[5-(3-azidopropylcarbamoyl)-2-carboxyphenyl]-7,7,19,19-tetramethyl-17-(sulfonatomethyl)-2-oxa-6,20-diazapentacyclo[12.8.0.03,12.05,10.016,21]docosa-1(22),3(12),4,8,10,13,15,17,20-nonaen-9-yl]methanesulfonate |
| SMILES | CC1(C=C(C2=CC3=C(C=C2N1)OC4=CC5=NC(C=C(C5=CC4=C3C6=C(C=CC(=C6)C(=O)NCCCN=[N+]=[N-])C(=O)O)CS(=O)(=O)[O-])(C)C)CS(=O)(=O)[O-])C.[K+].[K+] |
| InChI | InChI=1S/C36H36N6O10S2.2K/c1-35(2)15-20(17-53(46,47)48)23-11-26-30(13-28(23)40-35)52-31-14-29-24(21(18-54(49,50)51)16-36(3,4)41-29)12-27(31)32(26)25-10-19(6-7-22(25)34(44)45)33(43)38-8-5-9-39-42-37;;/h6-7,10-16,40H,5,8-9,17-18H2,1-4H3,(H,38,43)(H,44,45)(H,46,47,48)(H,49,50,51);;/q;2*+1/p-2 |
| InChIKey | SMJACSSSBQURHX-UHFFFAOYSA-L |
| Appearance | Dark Colored Solid |
Product Specification
| Excitation | 572 |
| Emission | 598 |
Application
AF 568 azide is a fluorescent azide building block designed for copper-free click chemistry labeling workflows. As an AF 568-derived dye, it provides orange-red fluorescence for tracking biomolecules and materials, while the azide handle enables efficient conjugation to cyclooctyne/DBCO- or strained-alkyne-functionalized targets. This combination makes it well suited for constructing fluorescent conjugates for imaging, assay development, and flow-based readouts where a robust dye attachment strategy is required.
1. Biomolecule Labeling
AF 568 azide is used by chemical biology and proteomics researchers to fluorescently label proteins, peptides, and other biomolecules via azide-alkyne click conjugation. In typical workflows, the azide dye is introduced to a cyclooctyne/DBCO-functionalized biomolecule or affinity reagent to generate stable fluorescent conjugates for downstream microscopy and fluorescence-based assays. The dye's AF 568 emission is commonly leveraged for multicolor experiments where orange-red channels are convenient, and the azide functional group supports modular probe construction without requiring dye redesign.
2. Fluorescence Microscopy Imaging
AF 568 azide supports fluorescence microscopy studies where researchers need a reactive dye for labeling biological samples and imaging structures with an orange-red readout. Investigators often incorporate the azide dye into labeling panels for fixed-cell imaging, cellular component tracking in labeled biomaterials, and visualization of tagged biomolecule populations. Because the labeling is driven by click-compatible functional handles rather than dye-specific coupling chemistries, AF 568 azide is frequently selected for building consistent fluorescent conjugates across experiments, including reagent sets used for comparative imaging and colocalization studies.
3. Flow Cytometry Staining
AF 568 azide is applied in flow cytometry workflows to generate fluorescently labeled targeting reagents and staining conjugates for population analysis. Researchers commonly use it to label antibody fragments, engineered binding proteins, or other DBCO/cyclooctyne-functionalized affinity reagents, enabling staining of labeled targets followed by fluorescence detection in an orange-red channel. The azide click handle is particularly useful for preparing reagent batches with standardized dye loading and for assembling multicolor panels where the AF 568 spectral region helps separate signals from other fluorophores.
4. Fluorescent Probe Construction
AF 568 azide is widely used in fluorescent probe development where modular dye attachment is required to create imaging reagents with defined targeting or reporting elements. Probe developers incorporate the azide dye into conjugation schemes by coupling it to cyclooctyne/DBCO-functionalized scaffolds such as affinity tags, polymer backbones, or nanoparticle surfaces, producing fluorescent constructs for assay development and molecular imaging experiments. This approach is commonly chosen when researchers want to rapidly swap targeting components while keeping the same AF 568 fluorophore for consistent optical readout across probe variants.
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