
Azido-PEG4-oxazolidin-2-one | CAS 1919045-03-6
| Catalog Number | R14-0128 |
| Category | Azides |
| Molecular Formula | C13H24N4O6 |
| Molecular Weight | 332.4 |
* Please be kindly noted products are not for therapeutic use. We do not sell to patients.
Product Introduction
Azido-PEG4-oxazolidin-2-one is a bifunctional crosslinker containing an azide group and an oxazolidin group. The azide group enables Click Chemistry. The Oxazolidin-2-onegroup is an efficient ligand for the copper-catalyzed N-arylation of pyrrole, imidazole and Iindole. The hydrophilic PEG spacer increases solubility in aqueous media.
Chemical Information
Product Specification
Application
Computed Properties
Chemical Information
| Synonyms | 2-Oxazolidinone, 3-(14-azido-3,6,9,12-tetraoxatetradec-1-yl)-; 3-[2-[2-[2-[2-(2-azidoethoxy)ethoxy]ethoxy]ethoxy]ethyl]-1,3-oxazolidin-2-one |
| Purity | 98% |
| IUPAC Name | 3-[2-[2-[2-[2-(2-azidoethoxy)ethoxy]ethoxy]ethoxy]ethyl]-1,3-oxazolidin-2-one |
| SMILES | C1COC(=O)N1CCOCCOCCOCCOCCN=[N+]=[N-] |
| InChI | InChI=1S/C13H24N4O6/c14-16-15-1-4-19-7-9-21-11-12-22-10-8-20-5-2-17-3-6-23-13(17)18/h1-12H2 |
| InChIKey | LQVWHKLBYQKZEO-UHFFFAOYSA-N |
Product Specification
| Storage | -20 °C |
Application
Azido-PEG4-oxazolidin-2-one is a PEGylated azide-bearing click chemistry reagent that combines an azide handle for bioorthogonal conjugation with an oxazolidin-2-one motif commonly used as a versatile electrophilic/functional group in chemical biology workflows. Its polyethylene glycol linker improves aqueous compatibility and reduces nonspecific interactions, making it well suited for labeling, surface functionalization, and reagent incorporation into larger molecular constructs. The presence of the azide enables downstream strain-promoted or catalyst-free click strategies for attaching the oxazolidin-2-one functionality to biomolecules, polymers, and imaging or diagnostic scaffolds.
1. Biomolecule Labeling
Azido-PEG4-oxazolidin-2-one is frequently used in bioconjugation workflows where researchers need to introduce a PEG-spaced azide handle into proteins, peptides, or nucleic-acid-associated constructs prior to click-based assembly of multifunctional probes. The reagent’s PEG4 spacing supports efficient conjugation and helps maintain solubility during buffer-exchange and purification steps typical of labeling pipelines. In practice, it is incorporated as a modular building block to generate intermediate conjugates that can be further functionalized with complementary click partners, enabling the construction of affinity reagents, binding probes, and multi-component chemical tools for mechanistic studies and assay development.
2. Surface And Material Functionalization
Azido-PEG4-oxazolidin-2-one is well aligned with materials chemistry use cases where azide-bearing linkers are required to create clickable surfaces for subsequent grafting or patterning. Researchers apply this reagent to functionalize polymer films, hydrogel networks, and biomaterial surfaces with PEG-mediated spacing that can improve accessibility of reactive sites and reduce steric hindrance for downstream conjugation. After immobilization or incorporation, the azide enables modular attachment of fluorescent tags, affinity ligands, or other functional moieties through click coupling, supporting the development of customizable platforms for biosensing, surface-based assays, and research-grade materials.
3. Molecular Imaging Probes
Azido-PEG4-oxazolidin-2-one is used as a chemical handle in the preparation of imaging and detection reagents that require controlled attachment of functional groups to targeting scaffolds or reporter constructs. The PEG4 linker helps maintain dispersion and reduces aggregation tendencies when probes are assembled in aqueous systems, which is particularly valuable during probe formulation and characterization. By leveraging the azide for click-compatible assembly, teams can generate probe intermediates that carry the oxazolidin-2-one functionality while enabling rapid conjugation to imaging reporters or signal-generating components, supporting iterative design of molecular imaging tools.
4. Diagnostic Reagent Development
Azido-PEG4-oxazolidin-2-one supports diagnostic-reagent workflows that rely on modular conjugation strategies to build assay-ready reagents with defined chemical composition and spacing. In many development settings, the reagent is used to introduce an azide-bearing PEG linker into antibody fragments, affinity binders, or assay components, allowing subsequent click-based installation of detection reporters or capture elements. The oxazolidin-2-one motif provides an additional functional handle for constructing multi-functional assay formats, while the PEG4 spacer promotes consistent behavior in buffered assay conditions and helps preserve accessibility of labeled groups for downstream assay assembly and reagent screening.
Computed Properties
| XLogP3 | 0.2 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 8 |
| Rotatable Bond Count | 15 |
| Exact Mass | 332.16958450 g/mol |
| Monoisotopic Mass | 332.16958450 g/mol |
| Topological Polar Surface Area | 80.8Ų |
| Heavy Atom Count | 23 |
| Formal Charge | 0 |
| Complexity | 364 |
| 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 |
Recommended Services
Recommended Articles
- Hoechst Dyes: Definition, Structure, Mechanism and Applications
- Mastering the Spectrum: A Comprehensive Guide to Cy3 and Cy5 Dyes
- Fluorescent Probes: Definition, Structure, Types and Application
- Fluorescent Dyes: Definition, Mechanism, Types and Application
- Coumarin Dyes: Definition, Structure, Benefits, Synthesis and Uses
- Unlocking the Power of Fluorescence Imaging: A Comprehensive Guide
- Cell Imaging: Definitions, Systems, Protocols, Dyes, and Applications
- Lipid Staining: Definition, Principles, Methods, Dyes, and Uses
- Flow Cytometry: Definition, Principles, Protocols, Dyes, and Uses
- Nucleic Acid Staining: Definition, Principles, Dyes, Procedures, and Uses
Recommended Products
Online Inquiry