
BCN-PEG4-hydrazide (exo)
| Catalog Number | R16-0034 |
| Category | BCN Reagents |
| Molecular Formula | C22H37N3O7 |
| Molecular Weight | 455.55 |
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Product Introduction
BCN-PEG4-hydrazide (exo) features a bicyclo[6.1.0]nonyne (BCN) moiety, which participates in strain-promoted azide-alkyne cycloaddition reactions, a hallmark of click chemistry. The incorporation of a PEG4 spacer enhances hydrophilicity, while the hydrazide functionality allows for subsequent conjugation with aldehydes or ketones, facilitating versatile bioconjugation strategies. This reagent is often employed in the modification of biomolecules, surface immobilization, and the development of multifunctional polymeric systems.
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-PEG4-hydrazide (exo) is a BCN-functionalized, polyethylene glycol (PEG)-linked hydrazide designed for strain-promoted click chemistry with tetrazines, enabling bioorthogonal conjugation under mild conditions. The BCN handle provides a fast, selective reaction partner for tetrazine reagents, while the hydrazide offers a reactive site for subsequent coupling to aldehyde-bearing biomolecules, surfaces, or material scaffolds. This combination makes BCN-PEG4-hydrazide (exo) particularly relevant for modular labeling workflows in chemical biology, diagnostics reagent development, and biomaterials functionalization where controlled attachment and spacing are important.
1. Tetrazine-Based Probe Labeling
BCN-PEG4-hydrazide (exo) is used as a click-ready PEG spacer conjugate for preparing tetrazine-reactive labeling reagents and imaging probes. Researchers employ the BCN handle to install hydrazide-bearing functionality onto tetrazine-tagged carriers, nanoparticles, or probe platforms, improving solubility and reducing nonspecific interactions through the PEG segment. The resulting conjugates are commonly advanced into workflows that require a defined attachment point for downstream coupling chemistry, such as linking to aldehyde-functional targeting ligands, affinity reagents, or assay components.
2. Hydrazone Coupling to Aldehydes
BCN-PEG4-hydrazide (exo) supports two-stage assembly strategies in which the hydrazide functionality is leveraged to form hydrazone linkages with aldehyde-containing partners. This is widely used in research-grade conjugation pipelines for attaching biomolecules, polymers, and labeling moieties to hydrazide-bearing scaffolds after initial BCN-mediated click installation. The PEG4 spacing helps maintain accessibility of the hydrazide group and can improve conjugate homogeneity when immobilizing or decorating complex constructs such as probe libraries, affinity reagents, and reagent cartridges for analytical assays.
3. Surface and Material Functionalization
BCN-PEG4-hydrazide (exo) is applicable to the functionalization of biomaterial surfaces and engineered materials where PEG-mediated presentation of reactive groups is required. Teams in biomaterials science and chemical biology use the BCN handle to graft hydrazide-containing PEG linkers onto tetrazine-functionalized coatings, films, or particle surfaces, creating stable, addressable interfaces for subsequent aldehyde-driven coupling. This approach is commonly used to generate reproducible functional surfaces for binding studies, reagent immobilization, and modular construction of multi-component material systems.
4. Molecular Imaging and Diagnostics Reagents
BCN-PEG4-hydrazide (exo) is routinely incorporated into the build-out of molecular imaging and diagnostic reagent platforms that rely on modular conjugation and controlled linker architecture. The BCN click handle enables rapid installation onto tetrazine-bearing imaging or capture components, while the hydrazide group provides a practical handle for connecting to aldehyde-functional reporters, tags, or recognition elements. In diagnostic reagent development and chemical biology tool creation, this reagent supports flexible assembly of labeled constructs and multiplex-ready probe formats where spacing and reactive-site accessibility are critical for consistent performance in assay workflows.
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