
BCN-PEG4-alkyne (exo)
| Catalog Number | R16-0046 |
| Category | BCN Reagents |
| Molecular Formula | C22H33NO6 |
| Molecular Weight | 407.59 |
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Product Introduction
BCN-PEG4-alkyne (exo) features a bicyclononyne (BCN) moiety conjugated to an alkyne group through a four-unit polyethylene glycol (PEG4) spacer. This reagent participates in strain-promoted azide-alkyne cycloaddition (SPAAC) reactions, facilitating copper-free click chemistry applications in bioconjugation and labeling. The PEG4 linker enhances solubility and flexibility, supporting its incorporation into surface modification and polymer functionalization strategies.
Chemical Information
Product Specification
Application
Chemical Information
| Purity | >95% |
| Solubility | DCM, THF, acetonitrile, DMF and DMSO |
| Appearance | Oil |
Product Specification
| Storage | -80 °C |
Application
BCN-PEG4-alkyne (exo) is a bicyclononyne (BCN) click chemistry reagent bearing a PEG4 linker and a terminal alkyne handle, enabling strain-promoted cycloaddition for efficient bioconjugation in aqueous conditions. The exo-oriented BCN functionality and flexible PEG spacer are commonly leveraged to improve conjugation accessibility and reduce steric effects in labeling workflows. As a bifunctional click-ready construct, BCN-PEG4-alkyne (exo) is frequently incorporated into chemical biology and biomaterials programs that require modular attachment points for downstream imaging, surface patterning, or multi-step conjugation strategies.
1. Live-Cell Surface Labeling
BCN-PEG4-alkyne (exo) is widely used for labeling cell surfaces and extracellular biomolecules where rapid, catalyst-free click reactions are advantageous for preserving sensitive biological structures. Researchers in chemical biology and imaging groups often choose this reagent when they need a PEG-mediated spacer to improve reach to membrane-proximal targets and to support consistent conjugation across heterogeneous surfaces. The alkyne handle also supports orthogonal follow-up chemistry, allowing sequential installation of reporters, affinity tags, or secondary probes without redesigning the primary labeling step.
2. Protein and Peptide Conjugation
BCN-PEG4-alkyne (exo) serves as a practical coupling component for generating BCN-functional protein or peptide conjugates used in assay development and reagent construction. In bioconjugation workflows, the PEG4 linker helps maintain solubility and reduces nonspecific aggregation that can complicate labeling of biomacromolecules, while the BCN moiety provides a robust click handle for attaching to azide-bearing partners. Many laboratories employ BCN-PEG4-alkyne (exo) to build modular reagent sets for studying biomolecular interactions, preparing labeled standards, or creating multi-component probe libraries with consistent spacing and improved handling.
3. Biomaterials Surface Functionalization
BCN-PEG4-alkyne (exo) is commonly applied to functionalize polymeric and hydrogel materials with clickable moieties for constructing biointerfaces, coatings, and patterned surfaces. Biomaterials scientists use the PEG4 spacer to promote uniform presentation of the reactive BCN group at the material interface, which can be critical for reproducible conjugation density and accessibility. The resulting BCN-functional surfaces can be further coupled to azide-containing ligands or imaging tags, supporting iterative design of materials for cell-interaction studies, biosensing platforms, and customizable surface chemistries.
4. Multi-Step Probe Construction
BCN-PEG4-alkyne (exo) is particularly useful in multi-step labeling and probe assembly pipelines where an initial BCN-based click installation is followed by additional orthogonal modifications via the alkyne functionality. Molecular imaging and diagnostic reagent developers often integrate this reagent into workflows that require staged incorporation of fluorophores, affinity elements, or enrichment handles while keeping the overall probe architecture modular. The PEG4 linker contributes to improved solubility and reduced steric congestion, helping maintain probe performance during conjugation and purification steps used to prepare complex research reagents.
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