
bis-PEG2-endo-BCN | CAS 1476737-97-9
| Catalog Number | R16-0006 |
| Category | BCN Reagents |
| Molecular Formula | C28H40N2O6 |
| Molecular Weight | 500.63 |
* Please be kindly noted products are not for therapeutic use. We do not sell to patients.
Product Introduction
bis-PEG2-endo-BCN is a bifunctional ADC linker with two endo-BCN groups connected via PEG2 spacer, facilitating dual strain-promoted click conjugations in antibody-drug conjugate synthesis.
Chemical Information
Product Specification
Application
Chemical Information
| Synonyms | bis(bicyclo[6.1.0]non-4-yn-9-ylmethyl) ((ethane-1,2-diylbis(oxy))bis(ethane-2,1-diyl))dicarbamate |
| Purity | >98.0% |
| Shelf Life | -20°C 3 years powder; -80°C 2 years in solvent |
| IUPAC Name | |
| SMILES | C1CC2C(C2COC(=O)NCCOCCOCCNC(=O)OCC3C4C3CCC#CCC4)CCC#C1 |
| InChI | InChI=1S/C28H40N2O6/c31-27(35-19-25-21-9-5-1-2-6-10-22(21)25)29-13-15-33-17-18-34-16-14-30-28(32)36-20-26-23-11-7-3-4-8-12-24(23)26/h21-26H,5-20H2,(H,29,31)(H,30,32) |
| InChIKey | NISHVKOYJUQOBR-UHFFFAOYSA-N |
| Solubility | 10 mm in DMSO |
| Appearance | Solid |
Product Specification
| Storage | Store at -20 °C, keep in dry and avoid sunlight. |
Application
bis-PEG2-endo-BCN is a bis-functional, PEGylated bicyclononyne (BCN) click chemistry reagent designed for strain-promoted azide–alkyne cycloaddition (SPAAC) with azides under copper-free conditions. The endo-BCN architecture provides efficient reactivity toward azide partners, while the PEG2 spacer and bis-functional design support multivalent labeling and improved solubility in aqueous workflows. bis-PEG2-endo-BCN is commonly selected for building modular biomaterials, preparing functional imaging probes, and generating well-defined conjugates in chemical biology and diagnostics research.
1. Multivalent Biomolecule Labeling
bis-PEG2-endo-BCN is widely used to introduce two BCN reactive handles into azide-bearing biomolecules, enabling multivalent conjugation strategies that improve labeling density and conjugate homogeneity for downstream assays. Researchers commonly pair bis-PEG2-endo-BCN with azide-functional proteins, peptides, oligonucleotides, or cell-surface targeting constructs to generate defined dual-site adducts for mechanistic studies, binding assays, and platform development. The PEG2 spacing helps maintain aqueous compatibility and reduces nonspecific aggregation during conjugation and purification steps, making the reagent a practical choice for workflows that require consistent, reproducible functionalization.
2. Hydrogel And Surface Functionalization
bis-PEG2-endo-BCN supports copper-free click immobilization of BCN-bearing PEG constructs onto azide-functional hydrogels and polymer surfaces, facilitating rapid fabrication of functional biomaterials. Biomaterials groups use this reagent to pattern or crosslink azide-containing matrices, incorporate bioorthogonal ligands, and tune surface chemistry for cell-interaction studies and materials characterization. The bis-functional nature is particularly useful when dual attachment points are desired to enhance network stability or to control ligand presentation on scaffolds and coatings used in laboratory-scale device prototyping and materials screening.
3. Molecular Imaging Probe Construction
bis-PEG2-endo-BCN is commonly incorporated into molecular imaging and detection reagent development as a modular BCN building block for attaching azide-tagged fluorophores, affinity moieties, or reporter groups. Chemical biology teams rely on the PEGylated bis-BCN format to improve solubility and to support controlled multivalent probe assembly, which can be advantageous when designing higher-affinity labeling reagents or signal-amplified constructs for microscopy and analytical workflows. The copper-free SPAAC compatibility also aligns with sensitive labeling environments where minimizing metal exposure is important for preserving probe integrity during conjugation.
4. Diagnostic Reagent And Assay Platforms
bis-PEG2-endo-BCN is used in the preparation of research diagnostic reagents and assay components that require bioorthogonal coupling to azide-functional capture elements, reporters, or assay surfaces. Suppliers and academic groups often select this reagent to assemble dual-functional conjugates, such as linking azide-bearing detection labels to azide-presenting assay formats, including bead-based assays and microarray-style reagent libraries. The bis-functional PEG2 scaffold helps streamline reagent handling in aqueous buffers and supports scalable conjugation workflows used for method development, reagent optimization, and assay prototyping.
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