
m-PEG2-DBCO
| Catalog Number | R01-0368 |
| Category | Cycloalkyne Dyes (DBCO) |
| Molecular Formula | C24H26N2O4 |
| Molecular Weight | 406.5 |
* Please be kindly noted products are not for therapeutic use. We do not sell to patients.
Product Introduction
m-PEG2-DBCO features a dibenzocyclooctyne (DBCO) moiety conjugated to a two-unit methoxy polyethylene glycol (m-PEG) chain, facilitating bioorthogonal labeling and conjugation processes. The DBCO group enables strain-promoted azide-alkyne cycloaddition (SPAAC), allowing for copper-free click chemistry reactions with azide-functionalized molecules. This reagent is commonly used in the modification of biomolecules, surface immobilization, and the development of PEGylation strategies, offering a robust platform for bioconjugation and polymer functionalization in diverse experimental settings.
Chemical Information
Product Specification
Application
Computed Properties
Patents
Chemical Information
| IUPAC Name | 4-(2-azatricyclo[10.4.0.04,9]hexadeca-1(16),4,6,8,12,14-hexaen-10-yn-2-yl)-N-[2-(2-methoxyethoxy)ethyl]-4-oxobutanamide |
| SMILES | COCCOCCNC(=O)CCC(=O)N1CC2=CC=CC=C2C#CC3=CC=CC=C31 |
| InChI | InChI=1S/C24H26N2O4/c1-29-16-17-30-15-14-25-23(27)12-13-24(28)26-18-21-8-3-2-6-19(21)10-11-20-7-4-5-9-22(20)26/h2-9H,12-18H2,1H3,(H,25,27) |
| InChIKey | MSDBUVAFXGJQTF-UHFFFAOYSA-N |
Product Specification
| Storage | -20 °C |
Application
m-PEG2-DBCO is a polyethylene glycol (PEG)-tethered DBCO (dibenzocyclooctyne) cyclooctyne designed for strain-promoted azide–alkyne cycloaddition (SPAAC) click chemistry. The reagent combines a bioinert PEG spacer with a highly reactive cyclooctyne handle, enabling efficient, catalyst-free conjugation under mild aqueous conditions. Its compact, water-compatible architecture makes it a widely used building block for preparing azide-functional biomolecules, surfaces, and materials for downstream labeling, assembly, and imaging workflows.
1. Biomolecule PEGylation
m-PEG2-DBCO is commonly used to introduce a PEG spacer onto azide-bearing proteins, peptides, antibodies, and nucleic-acid reagents via SPAAC, supporting improved solubility and reduced nonspecific interactions in complex assay buffers. Researchers often select this reagent when they need a short, defined PEG length that preserves binding or recognition elements while providing steric shielding and better handling during conjugate preparation. The DBCO functionality enables rapid attachment to azide tags without copper catalysts, which is advantageous for sensitive biomolecule formats and for workflows that prioritize operational simplicity and reproducibility.
2. Surface And Material Functionalization
m-PEG2-DBCO is frequently applied to functionalize azide-present surfaces and polymeric materials, including hydrogel platforms, bead-based supports, and microfabricated substrates used in chemical biology and materials research. The PEG spacer helps tune interfacial properties such as hydration, protein adsorption, and accessibility of the reactive site, which is particularly relevant when immobilizing affinity ligands or creating patterned binding regions. By using SPAAC chemistry, teams can attach DBCO-bearing PEG linkers to azide-functional coatings under conditions compatible with many material chemistries and device assembly constraints.
3. Multicolor Probe And Imaging Conjugates
m-PEG2-DBCO is a practical reagent for constructing azide-tagged fluorescent probes and imaging reagents, where a PEG spacer can improve dispersion, reduce aggregation, and enhance labeling uniformity in probe formulations. Molecular imaging and assay development groups often incorporate m-PEG2-DBCO to couple imaging handles to azide-functional targeting components, enabling modular assembly of probe libraries with consistent linker length. The catalyst-free nature of SPAAC supports integration into iterative labeling pipelines, including rapid exchange of probe components for optimization of signal-to-background in research assays.
4. Targeted Delivery Platform Building
m-PEG2-DBCO is used as a click-ready PEG linker in the preparation of modular delivery and carrier-like research constructs, where azide-functional targeting ligands or surface components are assembled onto DBCO-functionalized scaffolds. The short PEG segment can help regulate surface presentation and accessibility of conjugated moieties, which matters for reproducible assembly of multicomponent platforms such as ligand-decorated nanoparticles, vesicle-like systems, and scaffolded carrier materials used in chemical biology tool development. This reagent supports streamlined conjugation workflows that avoid copper catalysts, which can be important for maintaining the integrity of complex, multi-domain constructs during preparation.
Computed Properties
| XLogP3 | 1.8 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 4 |
| Rotatable Bond Count | 9 |
| Exact Mass | 406.18925731 g/mol |
| Monoisotopic Mass | 406.18925731 g/mol |
| Topological Polar Surface Area | 67.9Ų |
| Heavy Atom Count | 30 |
| Formal Charge | 0 |
| Complexity | 638 |
| 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 |
Patents
| Publication Number | Title | Priority Date |
|---|---|---|
| US-2022016252-A1 | Immuno oncology combination therapy with il-2 conjugates and anti-egfr antibodies | 2020-06-25 |
| US-2022401561-A1 | Protein-macromolecule conjugates and methods of use thereof | 2019-09-30 |
| US-2022016249-A1 | IL-2 Conjugates and Methods of Use Thereof | 2019-02-06 |
| US-10746731-B2 | Surface immobilization of an analyte-recognizing molecule | 2015-06-30 |
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