
BCN-PEG4-HyNic (exo)
| Catalog Number | R16-0050 |
| Category | BCN Reagents |
| Molecular Formula | C28H41N5O6 |
| Molecular Weight | 543.65 |
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Product Introduction
BCN-PEG4-HyNic (exo) features a bicyclo[6.1.0]nonyne (BCN) moiety, which participates in strain-promoted azide-alkyne cycloaddition reactions, facilitating bioorthogonal conjugation processes. The compound is equipped with a PEG4 spacer, providing enhanced solubility and flexibility in linker design, crucial for surface modification and polymer functionalization applications. Additionally, the incorporation of a HyNic group allows for hydrazone formation, enabling efficient bioconjugation and labeling of biomolecules in diverse experimental contexts.
Chemical Information
Product Specification
Application
Chemical Information
| Purity | >95% |
| Solubility | DCM, THF, acetonitrile, DMF and DMSO |
| Appearance | Colorless oil |
Product Specification
| Storage | -20 °C |
Application
BCN-PEG4-HyNic (exo) is a BCN-functionalized, PEG4-linked hydrazine/nucleophile reagent designed for strain-promoted click chemistry and widely used in bioorthogonal labeling workflows. The bicyclononyne (BCN) handle enables rapid, catalyst-free conjugation to complementary azide-bearing partners, while the HyNic moiety provides an orthogonal reactive element commonly leveraged for probe assembly and multicomponent targeting strategies. Its PEG spacer supports aqueous solubility and improves conjugation accessibility, making it a practical building block for fluorescent, affinity, and imaging reagent development.
1. Live-Cell Surface Labeling
BCN-PEG4-HyNic (exo) is used to install BCN-bearing conjugates on cell-surface or membrane-associated biomolecules for downstream azide-reactive tagging in cellular assays. Researchers commonly incorporate this reagent into labeling schemes where PEG-mediated spacing helps maintain accessibility of the click handle, supporting efficient coupling to azide-functional probes such as fluorophores, affinity tags, or imaging reporters. The HyNic functionality is often retained for additional orthogonal assembly steps, enabling modular workflows that separate surface installation from final probe generation.
2. Fluorescent Probe Conjugation
BCN-PEG4-HyNic (exo) serves as a versatile linker for constructing fluorescent conjugates where BCN-driven click coupling is used to attach dyes to biomolecule scaffolds. In probe development pipelines, the PEG4 spacer helps reduce steric constraints and supports consistent labeling across protein, peptide, or polymer carriers bearing azide groups. The HyNic group is frequently used as a complementary reactive handle during multistep reagent assembly, allowing researchers to generate probe sets with controlled stoichiometry and orthogonal functionalization for microscopy and assay readouts.
3. Molecular Imaging Reagent Assembly
BCN-PEG4-HyNic (exo) is applied in the preparation of molecular imaging platforms that rely on modular conjugation strategies. Teams developing imaging reagents often use BCN click chemistry to rapidly couple the BCN-bearing component to azide-functional imaging reporters or targeting constructs under mild conditions compatible with sensitive labeling reagents. The PEG4 linker contributes to improved aqueous behavior and spatial presentation of the BCN moiety, while the HyNic functionality supports additional conjugation logic for assembling multicomponent imaging probes and reagent libraries.
4. Biomaterials Surface Functionalization
BCN-PEG4-HyNic (exo) is used to functionalize biomaterial surfaces and interfaces with BCN-reactive groups for subsequent azide-based coupling steps. Materials scientists incorporate this reagent into coatings, hydrogel systems, and polymer conjugates to enable post-fabrication attachment of fluorescent markers, affinity ligands, or diagnostic reagent components via strain-promoted click chemistry. The PEG4 spacer helps mitigate surface crowding and promotes effective presentation of reactive sites, while the HyNic handle supports orthogonal modification routes during material-to-probe translation.
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