
DBCO-PEG4-triethoxysilane | CAS 2353410-02-1
| Catalog Number | R01-0347 |
| Category | Cycloalkyne Dyes (DBCO) |
| Molecular Formula | C₃₉H₅₇N₃O₁₀Si |
| Molecular Weight | 755.97 |
* Please be kindly noted products are not for therapeutic use. We do not sell to patients.
Product Introduction
DBCO-PEG4-triethoxysilane is a polyethylene glycol (PEG)-based PROTAC linker. DBCO-PEG4-triethoxysilane can be used in the synthesis of a series of PROTACs.
Chemical Information
Product Specification
Application
Computed Properties
Chemical Information
| Synonyms | 1-(4-{2-azatricyclo[10.4.0.0,hexadeca-1(16),4,6,8,12,14-hexaen-10-yn-2-yl}-4-oxobutanamido)-N-[3-(triethoxysilyl)propyl]-3,6,9,12-tetraoxapentadecan-15-amide |
| Purity | 98% |
| IUPAC Name | 4-(2-azatricyclo[10.4.0.04,9]hexadeca-1(16),4,6,8,12,14-hexaen-10-yn-2-yl)-4-oxo-N-[2-[2-[2-[2-[3-oxo-3-(3-triethoxysilylpropylamino)propoxy]ethoxy]ethoxy]ethoxy]ethyl]butanamide |
| SMILES | CCO[Si](CCCNC(=O)CCOCCOCCOCCOCCNC(=O)CCC(=O)N1CC2=CC=CC=C2C#CC3=CC=CC=C31)(OCC)OCC |
| InChI | InChI=1S/C39H57N3O10Si/c1-4-50-53(51-5-2,52-6-3)31-11-21-40-38(44)20-23-46-25-27-48-29-30-49-28-26-47-24-22-41-37(43)18-19-39(45)42-32-35-14-8-7-12-33(35)16-17-34-13-9-10-15-36(34)42/h7-10,12-15H,4-6,11,18-32H2,1-3H3,(H,40,44)(H,41,43) |
| InChIKey | BVPATRYMIHMPFW-UHFFFAOYSA-N |
| Solubility | DMSO, DCM, DMF |
Product Specification
| Storage | Please store the product under the recommended conditions in the Certificate of Analysis. |
Application
DBCO-PEG4-triethoxysilane is a bifunctional click chemistry reagent that combines a DBCO (dibenzocyclooctyne) strained-alkyne handle for copper-free strain-promoted azide–alkyne cycloaddition with a triethoxysilane group for surface attachment. The PEG4 spacer provides aqueous compatibility and molecular flexibility, enabling efficient presentation of the DBCO moiety on inorganic supports. This dual functionality makes it particularly relevant for building azide-functionalized bioconjugates, coatings, and imaging or sensing platforms on silica- and oxide-containing materials.
1. Surface Functionalization Coatings
DBCO-PEG4-triethoxysilane is widely used to create DBCO-presenting coatings on glass, silica, and other oxide-rich substrates via the triethoxysilane anchoring group. Researchers and materials scientists employ it to generate stable, covalently tethered click-ready surfaces that can subsequently react with azide-bearing biomolecules, polymers, or nanoparticles. The PEG4 linker helps reduce steric hindrance at the interface, supporting consistent grafting densities for downstream immobilization workflows used in biosurface engineering and assay development.
2. Immobilized Biomolecule Conjugation
DBCO-PEG4-triethoxysilane supports immobilization strategies where azide-functional targets are captured on silane-activated materials. Biomaterials groups use the reagent to attach enzymes, antibodies, peptides, or affinity ligands carrying azide tags to solid supports for creating reusable research tools such as functionalized microarrays, chromatography media, and immobilized affinity capture surfaces. The combination of a robust silane tether and a copper-free click handle is especially attractive for workflows that prioritize gentle conjugation conditions and reproducible surface presentation.
3. Nanoparticle And Bead Labeling
DBCO-PEG4-triethoxysilane is commonly applied to label silica-coated nanoparticles and porous silica beads with DBCO functionality prior to azide-mediated coupling. Molecular imaging and chemical biology laboratories use this approach to prepare clickable particulate probes for multivalent assembly, surface coating, and modular conjugation to azide-bearing targeting elements or reporters. The PEG4 spacer improves accessibility of the DBCO group on curved or high-surface-area materials, which is important for achieving uniform conjugation across heterogeneous particle populations.
4. Diagnostic Reagent Surface Platforms
DBCO-PEG4-triethoxysilane is used to build click-compatible diagnostic reagent surfaces where modular coupling of azide-tagged components is required. Diagnostic reagent developers and assay engineers incorporate the triethoxysilane chemistry to functionalize membrane-like or silica-based supports, then use strain-promoted azide–alkyne cycloaddition to assemble capture reagents, signal-generating components, or standardized reagent architectures. This platform approach enables rapid interchange of azide-functional reagents while maintaining a stable attachment layer on the underlying solid support.
Computed Properties
| Hydrogen Bond Donor Count | 2 |
| Hydrogen Bond Acceptor Count | 10 |
| Rotatable Bond Count | 28 |
| Exact Mass | 755.38132156 g/mol |
| Monoisotopic Mass | 755.38132156 g/mol |
| Topological Polar Surface Area | 143Ų |
| Heavy Atom Count | 53 |
| Formal Charge | 0 |
| Complexity | 1100 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently-Bonded Unit Count | 1 |
| Compound Is Canonicalized | Yes |
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