
DBCO-PEG23-amine TFA salt
| Catalog Number | R01-0400 |
| Category | Cycloalkyne Dyes (DBCO) |
| Molecular Formula | C69H114F3N3O27 |
| Molecular Weight | 1474.7 |
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Product Introduction
DBCO-PEG23-amine TFA salt 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
Computed Properties
Chemical Information
| Synonyms | DBCO-PEG23-amine |
| Purity | 98% |
| IUPAC Name | N-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-(2-aminoethoxy)ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethyl]-4-(2-azatricyclo[10.4.0.04,9]hexadeca-1(16),4,6,8,12,14-hexaen-10-yn-2-yl)-4-oxobutanamide |
| SMILES | C1C2=CC=CC=C2C#CC3=CC=CC=C3N1C(=O)CCC(=O)NCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCN |
| InChI | InChI=1S/C67H113N3O25/c68-13-15-73-17-19-75-21-23-77-25-27-79-29-31-81-33-35-83-37-39-85-41-43-87-45-47-89-49-51-91-53-55-93-57-59-95-60-58-94-56-54-92-52-50-90-48-46-88-44-42-86-40-38-84-36-34-82-32-30-80-28-26-78-24-22-76-20-18-74-16-14-69-66(71)11-12-67(72)70-61-64-7-2-1-5-62(64)9-10-63-6-3-4-8-65(63)70/h1-8H,11-61,68H2,(H,69,71) |
| InChIKey | NLDOMACCXIMRCH-UHFFFAOYSA-N |
Product Specification
| Storage | -20 °C |
Application
DBC0-PEG23-amine TFA salt is a DBCO-functionalized, PEGylated primary amine reagent designed for copper-free strain-promoted azide–alkyne cycloaddition (SPAAC). The long, flexible PEG spacer improves aqueous compatibility and reduces nonspecific interactions, while the terminal amine enables downstream coupling to activated carboxylic acids, NHS-esters, aldehydes, or isothiocyanates. As a result, DBC0-PEG23-amine TFA salt is widely used as a versatile click handle for building bioconjugates, surface-functional materials, and molecular imaging or diagnostic reagent platforms where stable attachment and controlled spacing are critical.
1. Bioconjugate Linker Design
DBC0-PEG23-amine TFA salt is commonly selected as a SPAAC-compatible linker for assembling multi-component bioconjugates, including antibody–polymer conjugates, protein–surface constructs, and ligand-decorated carriers. The DBCO group provides a robust, catalyst-free click site for reacting with azide-bearing biomolecules or affinity tags, while the PEG spacer helps maintain accessibility of the conjugated partners and supports homogeneous labeling in aqueous buffers. The terminal amine further supports secondary derivatization, enabling researchers to incorporate additional functional groups such as charge-modulating handles, chelators, or reactive moieties for stepwise construct assembly.
2. PEGylated Surface Functionalization
DBC0-PEG23-amine TFA salt is used to introduce SPAAC-reactive functionality onto polymer films, nanoparticles, and other material surfaces where controlled interfacial spacing is important. The PEG chain reduces steric crowding at the interface and can improve colloidal stability, making this reagent attractive for preparing azide-reactive coatings or for creating modular surfaces that can be further functionalized with azide-tagged biomolecules. The amine at the PEG terminus also supports additional surface chemistry workflows, such as coupling to carboxyl-functional substrates or linking to bifunctional crosslinkers used in materials development and assay platform fabrication.
3. Molecular Imaging Probe Assembly
DBC0-PEG23-amine TFA salt serves as a practical click component for constructing imaging and detection probes that require both a SPAAC handle and a defined attachment point for reporter integration. Researchers often use it to append azide-reactive targeting elements to fluorophores, affinity reagents, or other signal-bearing scaffolds, taking advantage of the PEG spacer to preserve probe performance by limiting quenching-prone proximity and nonspecific adsorption. The amine functionality enables convenient post-click conjugation to activated reporter derivatives, supporting modular probe generation for microscopy, fluorescence-based assays, and other optical or molecular detection tool development.
4. Diagnostic Reagent Platform Building
DBC0-PEG23-amine TFA salt is frequently incorporated into diagnostic reagent development workflows that rely on modular assembly of capture and detection components. By providing a DBCO click site for reaction with azide-functional reagents, it supports the construction of multivalent binding systems and reagent mixes where consistent spacing between functional groups improves binding accessibility and assay robustness. The terminal amine allows further customization of the conjugate architecture, supporting integration of additional reactive groups for immobilization on assay supports, coupling to affinity ligands, or incorporation of labels used in research-grade diagnostic assay formats.
Computed Properties
| XLogP3 | -2.3 |
| Hydrogen Bond Donor Count | 2 |
| Hydrogen Bond Acceptor Count | 26 |
| Rotatable Bond Count | 74 |
| Exact Mass | 1359.76631610 g/mol |
| Monoisotopic Mass | 1359.76631610 g/mol |
| Topological Polar Surface Area | 288Ų |
| Heavy Atom Count | 95 |
| Formal Charge | 0 |
| Complexity | 1730 |
| 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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