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5-(Azido-PEG4)-pent-2-yn-1-Ol
| Catalog Number | R14-0203 |
| Category | Azides |
| Molecular Formula | C13H23N3O5 |
| Molecular Weight | 301.3 |
* Please be kindly noted products are not for therapeutic use. We do not sell to patients.
Product Introduction
5-(Azido-PEG4)-pent-2-yn-1-Ol is a PEG linker containing an azide group and a terminal hydroxyl group. The hydrophilic PEG spacer increases solubility in aqueous media. The azide group can react with alkyne, BCN, DBCO via Click Chemistry to yield a stable triazole linkage. The hydroxyl group enables further derivatization or replacement with other reactive functional groups.
Chemical Information
Product Specification
Application
Computed Properties
Chemical Information
| Purity | 98% |
| IUPAC Name | 5-[2-[2-[2-(2-azidoethoxy)ethoxy]ethoxy]ethoxy]pent-2-yn-1-ol |
| SMILES | C(COCCOCCOCCOCCN=[N+]=[N-])C#CCO |
| InChI | InChI=1S/C13H23N3O5/c14-16-15-4-7-19-9-11-21-13-12-20-10-8-18-6-3-1-2-5-17/h17H,3-13H2 |
| InChIKey | YQCLXMHUARTLPW-UHFFFAOYSA-N |
Product Specification
| Storage | -20 °C |
Application
5-(Azido-PEG4)-pent-2-yn-1-Ol is a bifunctional, PEG-linked click chemistry building block that incorporates an azide handle and a terminal alkyne (propargyl alcohol motif) for orthogonal conjugation strategies. As a PEG4 spacer, it is commonly selected to improve solubility, reduce steric congestion, and tune linker length in probe and material assemblies. Its dual-reactive functionality makes it relevant for constructing modular biomolecule conjugates, surface coatings, and imaging or assay platforms that rely on copper-catalyzed azide–alkyne cycloaddition (CuAAC) or related click workflows.
1. Biomolecule Labeling Workflows
5-(Azido-PEG4)-pent-2-yn-1-Ol is widely used as a linker reagent to introduce a PEG spacer between a reactive biomolecule and downstream click partners, enabling efficient attachment of probes to proteins, peptides, or nucleic-acid derived constructs. Researchers often employ the azide or alkyne functionality depending on the complementary handle presented on the targeting component, allowing flexible design of conjugation schemes for mechanistic studies, binding assays, and analytical labeling. The PEG4 element helps maintain aqueous compatibility and can preserve the accessibility of the conjugated biomolecule, which is particularly valuable when building multi-component probe libraries.
2. Surface Functionalization And Coatings
5-(Azido-PEG4)-pent-2-yn-1-Ol supports the preparation of functional material surfaces where click chemistry is used to immobilize ligands, capture reagents, or reporter tags onto polymers, hydrogels, and microfabricated substrates. The PEG spacer is advantageous for creating antifouling-like spacing and improving the presentation of immobilized molecules away from the surface, which can enhance uniformity in array formats and improve reproducibility in surface-based assays. In practice, the reagent is selected to provide a robust, modular way to pattern reactive sites that can be further clicked with complementary azide or alkyne partners.
3. Molecular Imaging Probe Construction
5-(Azido-PEG4)-pent-2-yn-1-Ol is used to assemble imaging and detection probes that require controlled linker architecture between a reporter moiety and a targeting or affinity component. The dual functionality enables sequential or staged conjugation approaches, where the PEG4 spacer helps tune distance and reduce steric hindrance around the reporter group. Probe developers commonly incorporate such PEG-linked click handles to facilitate rapid exchange of targeting ligands or reporter chemistries while maintaining consistent chemical connectivity for comparative imaging reagent optimization.
4. Diagnostic And Assay Reagent Platforms
5-(Azido-PEG4)-pent-2-yn-1-Ol is a practical building block for preparing assay reagents that rely on click-based conjugation to generate multivalent detection constructs, including enzyme or polymer-linked readouts and affinity reagent assemblies. The PEG4 linker supports stable, water-compatible labeling and can help maintain the functional accessibility of immobilized or conjugated components in complex assay buffers. By providing a defined click handle for downstream coupling, the reagent is frequently used in workflows that require scalable reagent preparation for screening formats, calibration standards, and modular assay component libraries.
Computed Properties
| XLogP3 | 0.4 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 7 |
| Rotatable Bond Count | 14 |
| Exact Mass | 301.16377084 g/mol |
| Monoisotopic Mass | 301.16377084 g/mol |
| Topological Polar Surface Area | 71.5Ų |
| Heavy Atom Count | 21 |
| Formal Charge | 0 |
| Complexity | 333 |
| 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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