
Mal-PEG2-bis-PEG2-BCN (exo)
| Catalog Number | R16-0059 |
| Category | BCN Reagents |
| Molecular Formula | C57H87N7O18 |
| Molecular Weight | 1158.34 |
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Product Introduction
Mal-PEG2-bis-PEG2-BCN (exo) is a heterobifunctional reagent that integrates maleimide and bicyclononyne (BCN) moieties, facilitating orthogonal conjugation strategies in bioconjugation and click chemistry applications. The maleimide group provides selective reactivity towards thiol-containing biomolecules, enabling site-specific conjugation under mild conditions, while the BCN moiety participates in strain-promoted azide-alkyne cycloaddition (SPAAC) reactions, allowing for copper-free click chemistry. The incorporation of PEG spacers enhances solubility and flexibility, making this reagent suitable for linking biomolecules, modifying surfaces, and constructing complex macromolecular assemblies.
Chemical Information
Product Specification
Application
Chemical Information
| Purity | >90% |
| Solubility | DCM, THF, acetonitrile, DMF and DMSO |
| Appearance | Oil |
Product Specification
| Storage | -80 °C |
Application
Mal-PEG2-bis-PEG2-BCN (exo) is a BCN-functionalized, PEG-based click chemistry reagent designed for strain-promoted alkyne–cyclooctyne cycloaddition in aqueous and biomolecular settings. The structure combines a maleimide handle with a bis-PEG spacer architecture and an exo-oriented bicyclononyne (BCN) motif, enabling orthogonal conjugation workflows where the maleimide can be used to install the construct onto thiol-bearing targets and the BCN moieties provide subsequent rapid labeling. This reagent is commonly used in chemical biology, biomaterials functionalization, and molecular imaging tool development where multivalent PEG spacing improves solubility and reduces nonspecific interactions.
1. Thiol-Target Conjugation
Mal-PEG2-bis-PEG2-BCN (exo) is used to attach PEGylated BCN functionality to thiol-containing biomolecules and surface-reactive platforms via the maleimide handle, supporting downstream click labeling with BCN-compatible partners. Researchers in chemical biology and glycobiology frequently incorporate this reagent into workflows that require stable installation of a reactive cyclooctyne handle while maintaining colloidal stability and minimizing aggregation. The PEG spacers help preserve accessibility of the BCN group for subsequent strain-promoted cycloaddition, which is particularly valuable when conjugates must remain water-soluble and compatible with complex biological buffers.
2. Multivalent Probe Labeling
Mal-PEG2-bis-PEG2-BCN (exo) is well suited for preparing multivalent labeling reagents for microscopy, flow-based assays, and analytical imaging workflows that benefit from increased local probe density. The bis-PEG architecture and exo-oriented BCN functionality support efficient grafting onto BCN-reactive scaffolds, enabling researchers to build higher-avidity probe formats without relying on harsh conditions. This product is frequently selected when conjugation strategies must deliver reproducible labeling density and maintain probe performance in crowded media such as protein-rich solutions or polymer-containing formulations.
3. Biomaterials Surface Functionalization
Mal-PEG2-bis-PEG2-BCN (exo) is applied to functionalize biomaterial surfaces and polymeric matrices with click-reactive BCN groups, enabling modular post-fabrication assembly of coatings, capture layers, and patterned interfaces. Materials scientists use the maleimide for installing the reagent onto thiol-modified surfaces or tethered linkers, then use strain-promoted cycloaddition to attach fluorescent tags, affinity ligands, or other functional components under mild conditions. The PEG spacers contribute to hydration and steric control at the interface, which is important for reducing nonspecific adsorption and improving the uniformity of subsequent surface labeling.
4. Modular Imaging Reagent Building
Mal-PEG2-bis-PEG2-BCN (exo) supports the construction of modular molecular imaging reagents by providing a convenient BCN-bearing handle that can be coupled to complementary imaging reporters in a bioorthogonal manner. In molecular imaging and diagnostic reagent development, the reagent is often used to generate intermediate conjugates that can be rapidly assembled with fluorophores, affinity tags, or other imaging moieties through strain-promoted click chemistry. The PEG-based design helps maintain reporter dispersion and compatibility with labeling buffers, supporting consistent probe assembly for research-grade imaging workflows.
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