
Azido-PEG3-azide | CAS 101187-39-7
| Catalog Number | R14-0360 |
| Category | Azides |
| Molecular Formula | C8H16N6O3 |
| Molecular Weight | 244.25 |
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Product Introduction
1,11-Diazido-3,6,9-trioxaundecane (CAS# 101187-39-7) is a useful linker for biomolecules.
Chemical Information
Product Specification
Application
Chemical Information
| Synonyms | Azide-PEG4-Azide;1-azido-2-[2-[2-(2-azidoethoxy)ethoxy]ethoxy]ethane; 1-azido-2-[2-[2-(2-azidoethoxy)ethoxy]ethoxy]ethane |
| Purity | >95% |
| IUPAC Name | 1-azido-2-[2-[2-(2-azidoethoxy)ethoxy]ethoxy]ethane |
| SMILES | C(COCCOCCOCCN=[N+]=[N-])N=[N+]=[N-] |
| InChI | InChI=1S/C8H16N6O3/c9-13-11-1-3-15-5-7-17-8-6-16-4-2-12-14-10/h1-8H2 |
| InChIKey | SFMMXKLNFMIUCH-UHFFFAOYSA-N |
| Solubility | In DMSO: 100 mg/mL (409.42 mM; Need ultrasonic) |
| Appearance | Colorless clear liquid |
| LogP | 0.56232 |
Product Specification
| Storage | Pure form, -20°C, 3 years; 4°C, 2 years; In solvent, -80°C, 6 months; -20°C, 1 month |
| Signal | Warning |
| Precautionary Statement Codes | P264, P270, P301+P317, P330, and P501 |
Application
Azido-PEG3-azide is a PEG-based bifunctional azide reagent that serves as a versatile building block for click chemistry workflows. As a multi-azide substrate, it enables azide-to-alkyne conjugation strategies and is commonly used to introduce flexible PEG spacing between biomolecules, surfaces, or imaging labels. Its linear PEG3 linker and terminal azide groups make it particularly relevant for constructing multivalent conjugates, crosslinkable materials, and modular probe platforms in chemical biology and materials research.
1. Multivalent Probe Labeling
Azido-PEG3-azide is widely used to generate multivalent labeling reagents for chemical biology studies, where spacing and accessibility of reactive handles strongly influence downstream conjugation density. Researchers incorporate this PEG-diazide building block to extend the distance between a targeting moiety and a reporter, improving practical coupling to alkyne-functional dyes, affinity tags, or imaging ligands used in probe development. The bifunctional azide format supports iterative or parallel click steps, enabling the assembly of higher-order probe architectures such as dual-labeled constructs and modular sensor precursors.
2. Surface And Material Functionalization
Azido-PEG3-azide is commonly applied for functionalizing polymeric and solid-phase materials with azide handles that can be subsequently coupled to alkyne-bearing components via click chemistry. Biomaterials and coatings groups use it to tune surface hydrophilicity and reduce steric crowding by inserting a PEG spacer between the material interface and the reactive linkage. This reagent is especially useful when a material must present multiple conjugation sites for subsequent attachment of fluorescent reporters, affinity ligands, or capture molecules, supporting scalable workflows for assay substrate preparation and surface-reactive platform development.
3. Crosslinkable PEG Linkers
Azido-PEG3-azide is an effective PEG-based crosslinker precursor for creating networks and conjugate scaffolds that rely on azide functionality for orthogonal assembly with alkyne partners. In biomaterials science, it is used to introduce flexible, bioconjugation-ready spacing that can be translated into crosslinked hydrogels, tethered polymer conjugates, or multivalent linkages for immobilizing reagents on supports. The two terminal azides allow construction of defined connectivity patterns when paired with difunctional or multifunctional alkyne reagents, supporting reproducible formation of conjugate architectures used in research-grade material and interface engineering.
4. Modular Bioconjugation Platforms
Azido-PEG3-azide is frequently selected as a modular linker to prepare bioconjugation-ready intermediates for downstream click coupling to alkyne-functional biomolecules and probes. Chemical biology teams use it to standardize the introduction of PEG spacing and reactive azide termini, facilitating consistent assembly of conjugates such as dual-tag constructs, multicomponent labeling panels, and library-ready reagent sets. The PEG3 backbone helps maintain solubility and reduces nonspecific interactions during conjugate preparation, which is valuable for workflows that require robust handling of labeled reagents prior to final coupling steps.
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