
DBCO-PEG23-amine
| Catalog Number | R01-0398 |
| Category | Cycloalkyne Dyes (DBCO) |
| Molecular Formula | C67H113N3O25 |
| Molecular Weight | 1360.7 |
* Please be kindly noted products are not for therapeutic use. We do not sell to patients.
Product Introduction
DBCO-PEG23-amine is a PEG linker which contains DBCO and amine moieties. The DBCO group is commonly used in copper-free Click Chemistry reactions. The amine group is reactive with carboxylic acids, activated NHS esters, carbonyls (ketone, aldehyde) etc. The hydrophilic PEG spacer increases the water solubility of the compound.
Chemical Information
Product Specification
Application
Chemical Information
| Purity | 98% |
| Solubility | DMSO, DCM, DMF |
Product Specification
| Storage | -20 °C |
Application
DBCO-PEG23-amine is a strain-promoted azide-alkyne cycloaddition (SPAAC) click chemistry reagent built on a dibenzocyclooctyne (DBCO) cyclooctyne core, providing fast, catalyst-free conjugation to azide-bearing biomolecules and materials. The extended PEG23 spacer and terminal amine enable aqueous compatibility and versatile downstream coupling to activated carboxylates, NHS-esters, aldehydes, or other amine-reactive handles. This combination makes DBCO-PEG23-amine a widely used linker for preparing modular PEGylated probes, surface-functionalized platforms, and multivalent conjugates in chemical biology and biomaterials workflows.
1. Protein And Peptide Labeling
DBCO-PEG23-amine is commonly used to introduce a DBCO click handle into protein and peptide labeling workflows where azide-functional targets are already available, such as azide-tagged antibodies, engineered protein domains, or metabolically labeled biomolecules. The PEG23 chain helps reduce nonspecific interactions and improves colloidal stability in buffer, which is particularly useful when preparing soluble conjugates for imaging, binding studies, or analytical assays. The terminal amine further supports orthogonal functionalization steps, enabling researchers to tune charge, immobilization chemistry, or multivalent architectures before or after click conjugation.
2. Surface And Material Functionalization
DBCO-PEG23-amine is well suited for functionalizing biomaterials and material surfaces that require stable attachment of DBCO-bearing linkers prior to SPAAC with azide-containing coatings, nanoparticles, or biomolecular ligands. The PEG spacer supports better surface hydration and spacing control, which can improve accessibility of the click-reactive DBCO group on crowded interfaces. The amine handle enables straightforward immobilization onto activated surfaces or coupling to other linker systems used in biosensor fabrication, affinity materials, and polymer conjugates, supporting scalable workflows for preparing reusable or modular material platforms.
3. Multivalent Probe And Nanoconjugate Building
DBCO-PEG23-amine is frequently incorporated into multivalent probe design and nanoconjugate assembly, where controlling linker length and flexibility is critical for achieving effective presentation of reactive groups. By providing a DBCO moiety for SPAAC and a PEG23 spacer for steric tuning, this reagent supports the construction of higher-order conjugates such as PEGylated imaging probes, affinity reagents, and clustered ligand displays on nanoparticles or polymer backbones. The terminal amine enables additional conjugation steps to introduce targeting ligands, reporter handles, or secondary capture groups, facilitating iterative build-up of complex materials used in chemical biology research.
4. PEGylated Linker For Diagnostics Research
DBCO-PEG23-amine is used in diagnostic-reagent development and assay-reagent customization where PEG-based spacing and orthogonal chemistry are valuable for controlling reagent behavior in complex assay matrices. Researchers often employ this reagent to generate DBCO-functional intermediates that can be clicked onto azide-bearing detection components, including affinity reagents and labeled reporters, while maintaining improved solubility and reduced aggregation relative to shorter or more hydrophobic linkers. The amine functionality supports downstream coupling to assay-specific capture chemistries, enabling the creation of modular reagent formats for platform testing and method development in molecular diagnostics research environments.
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