
BCN-PEG3-OTs (exo)
| Catalog Number | R16-0056 |
| Category | BCN Reagents |
| Molecular Formula | C26H37NO8S |
| Molecular Weight | 523.64 |
* Please be kindly noted products are not for therapeutic use. We do not sell to patients.
Product Introduction
BCN-PEG3-OTs (exo) features a bicyclo[6.1.0]nonyne (BCN) moiety, which enables strain-promoted azide-alkyne cycloaddition (SPAAC) reactions, making it suitable for copper-free click chemistry applications. The presence of a PEG3 linker within its molecular architecture facilitates solubility and flexibility, allowing for effective conjugation with biomolecules or surfaces. As an exo isomer of BCN with a tosylate leaving group, it can participate in nucleophilic substitution reactions, serving as a versatile intermediate for further functionalization or surface modification tasks.
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-PEG3-OTs (exo) is a BCN-based, PEG3-linked click chemistry reagent designed for strain-promoted cycloaddition with tetrazines, enabling efficient bioorthogonal labeling in complex chemical and biological environments. The molecule incorporates a BCN (bicyclononyne) reactive handle and an OTs leaving group that supports robust conjugation workflows to activated nucleophiles or surfaces, while the PEG3 spacer improves solubility and reduces nonspecific interactions. BCN-PEG3-OTs (exo) is commonly used in research settings where modular attachment of functional groups, probes, or materials is required prior to tetrazine-mediated imaging or enrichment.
1. Tetrazine Bioorthogonal Labeling
BCN-PEG3-OTs (exo) is widely used as a BCN-functional intermediate for building tetrazine-reactive imaging and detection reagents, particularly when a PEG spacer is needed to maintain accessibility of the cycloaddition handle. Researchers incorporate this BCN-PEG3 unit into labeling constructs for tracking biomolecules, mapping interaction partners, and generating multi-component probe libraries where subsequent tetrazine conjugation provides a high-contrast, orthogonal coupling step. The exo BCN orientation and PEG3 tether help preserve reactivity and accessibility in crowded labeling conditions, making the reagent a practical choice for workflows that prioritize modular probe assembly and reproducible conjugation chemistry.
2. Surface And Material Functionalization
BCN-PEG3-OTs (exo) supports downstream functionalization of polymeric and inorganic surfaces through its OTs-derived conjugation handle, enabling the immobilization of BCN-bearing linkers onto prepared substrates. Materials scientists and chemical engineers use BCN-PEG3-OTs (exo) to create tetrazine-reactive surfaces for affinity capture, spatially resolved labeling, and reagent patterning in assays and research platforms. The PEG3 spacer is particularly valuable for reducing steric hindrance at the interface, improving the accessibility of the BCN group for later tetrazine-based coupling to fluorescent tags, affinity moieties, or reporter constructs.
3. Probe And Tag Conjugate Assembly
BCN-PEG3-OTs (exo) is commonly employed to assemble research-grade probe conjugates where a BCN handle must be installed onto a targeting scaffold, linker system, or reporter-bearing platform. In molecular imaging and chemical biology tool development, this reagent is used to generate BCN-functional intermediates that can be rapidly transformed into final tetrazine-reactive imaging agents, enrichment reagents, or multiplexing toolkits. The PEG3 linker provides a balance between solubility and functional-group spacing, helping maintain consistent labeling behavior across different conjugation formats such as small-molecule tags, polymeric probes, and modular affinity reagents.
4. Enrichment And Pull-Down Workflows
BCN-PEG3-OTs (exo) is used to prepare enrichment handles that can be coupled to tetrazine-tagged reporters for selective capture and downstream analysis in chemical biology and analytical chemistry workflows. By installing BCN onto a solid support or an affinity-compatible intermediate, laboratories can perform sequential labeling and retrieval steps that improve signal-to-background in complex mixtures. This reagent is especially useful when the chemistry requires a reliable BCN-bearing platform that remains accessible after conjugation, allowing efficient subsequent tetrazine-mediated attachment of detection or processing components during assay development and method optimization.
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