
Pyrene azide 1 | CAS 2135330-58-2
| Catalog Number | F08-0007 |
| Category | Pyrene Dyes |
| Molecular Formula | C23H22N4O3 |
| Molecular Weight | 402.45 |
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Product Introduction
Pyrene is a polyaromatic hydrocarbon with strong short-wavelength fluorescence. Unlike other fluorescent dyes, polyaromatic hydrocarbons are fluorescent probes with strong sensitivity to microenvironment. Thus, its fluorescence is different in polar, and nonpolar environments. Other effects can also be observed.,When two pyrenes are in close proximity, they form excimers. Excimer formation can be easily observed, and quantitatively estimated using fluorescent spectra.,Pyrene azide is a reagent for easy pyrene Click Chemistry labeling of any alkyne-bearing molecule. It allows to turn any molecule into pyrene-bearing probe.,This azide contains hydrophilic triethyleneglycol linker to mitigate intrinsic pyrene hydrophobicity, and facilitate attachment to biomolecules in aqueous solutions.,Another pyrene azide for Click Chemistry labeling is also available: Pyrene azide 2.
Chemical Information
Product Specification
Application
Chemical Information
| Purity | NMR 1H (95%) |
| Solubility | Soluble in dichloromethane, chloroform, moderately Soluble in DMSO, DMF, acetonitrile |
| Appearance | Yellowish solid |
Product Specification
| Excitation | 343; 326; 313; 276; 265; 242; 234 |
| Emission | 377; 397 |
| Storage | 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
Pyrene azide 1 is an azide-functionalized pyrene fluorophore designed for click chemistry-enabled incorporation into labeled biomolecules and materials. Its extended aromatic pyrene core provides strong fluorescence that is frequently leveraged for sensitive tracking in chemical biology workflows, while the azide handle enables efficient bioorthogonal conjugation to alkyne partners for probe and surface construction.
1. Fluorescent Biomolecule Labeling
Pyrene azide 1 is used as a fluorescent labeling building block in bioconjugation workflows where researchers need robust aromatic fluorescence to track proteins, peptides, and other biomolecules after conjugation. In practice, the azide functionality is employed to install the pyrene fluorophore onto alkyne-bearing targets, enabling fluorescent tagging for downstream imaging, binding studies, and reagent development. This approach is common in chemical biology and biomaterials laboratories that require stable, bright labeling for conjugates used in microscopy and fluorescence readouts.
2. Click-Constructed Fluorescent Probes
Pyrene azide 1 serves as a practical fluorophore component for constructing fluorescent probes and assay reagents through azide-alkyne click conjugation. Researchers incorporate the pyrene label into probe scaffolds to create fluorescent reporters that can be integrated into larger detection formats, including labeled affinity reagents and modular imaging constructs. The pyrene emission is particularly useful when a strong, easily excited fluorescence signal is desired for monitoring probe localization in complex mixtures or for tracking probe-bearing conjugates in workflow development.
3. Surface and Polymer Functionalization
Pyrene azide 1 is widely applied for fluorescent surface engineering and polymer functionalization where azide-to-alkyne click coupling is used to immobilize fluorescent moieties on materials. Materials scientists and biomaterials groups use it to generate fluorescently traceable surfaces, coatings, and functional polymers that can be visualized by fluorescence microscopy or used as fluorescent markers in material characterization studies. The pyrene label provides a convenient way to confirm grafting, distribution, and retention of functional groups on engineered substrates.
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