
BCN-PEG3-oxyamine (exo)
| Catalog Number | R16-0049 |
| Category | BCN Reagents |
| Molecular Formula | C21H35N3O7 |
| Molecular Weight | 441.52 |
* Please be kindly noted products are not for therapeutic use. We do not sell to patients.
Product Introduction
BCN-PEG3-oxyamine (exo) features a bicyclononyne (BCN) moiety, which participates in strain-promoted azide-alkyne cycloaddition reactions, enabling copper-free click chemistry applications. The incorporation of a PEG3 spacer enhances solubility and flexibility, facilitating its use in diverse bioconjugation and surface modification contexts. The oxyamine functional group allows for further conjugation strategies, making it suitable for applications in polymer functionalization and bioorthogonal chemistry.
Chemical Information
Product Specification
Application
Chemical Information
| Purity | >90% |
| Solubility | DCM, THF, acetonitrile, DMF and DMSO |
| Appearance | Colorless oil |
Product Specification
| Storage | -20 °C |
Application
BCN-PEG3-oxyamine (exo) is a BCN-functionalized, PEG3-spaced click chemistry reagent designed for bioorthogonal labeling workflows that commonly rely on strain-promoted cycloaddition chemistry. The molecule couples a BCN (bicyclononyne) handle with an oxyamine functionality, providing a convenient modular platform for introducing reactive oxime-forming chemistry onto biomolecules, surfaces, and polymeric constructs. Its PEG3 spacer supports aqueous compatibility and reduces steric constraints, which is valuable in probe development, imaging reagent assembly, and materials functionalization where controlled conjugation is required.
1. Bioorthogonal Probe Labeling
BCN-PEG3-oxyamine (exo) is used to generate labeling reagents for chemical biology studies where BCN-mediated capture is paired with downstream oxime-related conjugation strategies. Researchers incorporate this reagent into workflows for tagging proteins, peptides, and other biomolecular targets in complex buffers, enabling the installation of an oxyamine-bearing handle that can be carried through to subsequent affinity capture, enrichment, or analytical readouts. The PEG3 spacing helps maintain labeling efficiency and improves compatibility with labeling of sensitive biomolecular systems, supporting routine probe preparation for microscopy, flow-based assays, and analytical chemistry.
2. Surface And Material Functionalization
BCN-PEG3-oxyamine (exo) is well suited for functionalizing polymer and biomaterial surfaces with a reactive oxyamine-containing motif while leveraging BCN-based bioorthogonal attachment to preinstalled BCN-compatible surfaces or linkers. Materials scientists use it to introduce defined chemical functionality for building responsive coatings, immobilized capture surfaces, and modular interfaces for biosensing and research-grade diagnostic reagent development. The reagent’s PEG3 linker contributes to surface accessibility, which is important when attaching reactive groups to high-aspect-ratio materials such as hydrogels, membranes, and microstructured substrates.
3. Imaging And Molecular Diagnostics Tooling
BCN-PEG3-oxyamine (exo) supports the assembly of molecular imaging and diagnostic tooling by providing a BCN-reactive handle that can be incorporated into probe design pipelines. Chemical biology teams use the reagent to install oxyamine functionality on imaging scaffolds, enabling later conjugation to reporter moieties, affinity ligands, or signal-generating components used in research imaging platforms. The exo-oriented BCN/oxyamine architecture and PEG3 spacer are commonly leveraged to improve conjugation consistency across probe batches, which is particularly useful for building standardized reagent sets for instrument-based characterization.
4. Protein Conjugation Workflows
BCN-PEG3-oxyamine (exo) is applied in protein conjugation workflows where researchers need a robust chemical handle for constructing multi-component bioconjugates. The BCN functionality enables selective coupling to BCN-reactive partners in bioorthogonal labeling schemes, while the oxyamine group provides a practical chemical motif for subsequent derivatization steps used to generate conjugated protein reagents, affinity reagents, and analytical standards. Laboratories in chemical biology and biomaterials research often choose this reagent when they want PEG-mediated spacing to support efficient modification without excessive aggregation or loss of functional accessibility.
Recommended Services
Recommended Articles
- Hoechst Dyes: Definition, Structure, Mechanism and Applications
- Mastering the Spectrum: A Comprehensive Guide to Cy3 and Cy5 Dyes
- Fluorescent Probes: Definition, Structure, Types and Application
- Fluorescent Dyes: Definition, Mechanism, Types and Application
- Coumarin Dyes: Definition, Structure, Benefits, Synthesis and Uses
- Unlocking the Power of Fluorescence Imaging: A Comprehensive Guide
- Cell Imaging: Definitions, Systems, Protocols, Dyes, and Applications
- Lipid Staining: Definition, Principles, Methods, Dyes, and Uses
- Flow Cytometry: Definition, Principles, Protocols, Dyes, and Uses
- Nucleic Acid Staining: Definition, Principles, Dyes, Procedures, and Uses
Recommended Products
Online Inquiry