
Azido-PEG6-alcohol | CAS 86770-69-6
| Catalog Number | R14-0216 |
| Category | Azides |
| Molecular Formula | C12H25N3O6 |
| Molecular Weight | 307.34 |
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Product Introduction
Azido-PEG6-alcohol is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs. Azido-PEG6-alcohol is also a non-cleavable 6 unit PEG ADC linker used in the synthesis of antibody-drug conjugates (ADCs).
Chemical Information
Product Specification
Application
Computed Properties
Patents
Chemical Information
| Synonyms | N3-PEG6-OH; 17-azido-3,6,9,12,15-pentaoxaheptadecan-1-ol |
| Purity | >98.0% |
| Shelf Life | 0-4°C for short term (days to weeks), or -20°C for long term (months). |
| IUPAC Name | 2-[2-[2-[2-[2-(2-azidoethoxy)ethoxy]ethoxy]ethoxy]ethoxy]ethanol |
| SMILES | C(COCCOCCOCCOCCOCCO)N=[N+]=[N-] |
| InChI | InChI=1S/C12H25N3O6/c13-15-14-1-3-17-5-7-19-9-11-21-12-10-20-8-6-18-4-2-16/h16H,1-12H2 |
| InChIKey | DPRULTZUGLDCPZ-UHFFFAOYSA-N |
| Solubility | 10 mm in DMSO |
| Appearance | Solid |
Product Specification
| Storage | Store at -20 °C, keep in dry and avoid sunlight. |
Application
Azido-PEG6-alcohol is a PEG-based azide building block designed for copper-free and copper-mediated click chemistry workflows, enabling efficient installation of azide functionality onto hydroxyl-containing surfaces, linkers, and polymeric or biomaterial scaffolds. Its flexible PEG spacer (PEG6) and terminal alcohol support solubility and conjugation handle compatibility, making it a widely used reagent for preparing clickable intermediates prior to downstream bioconjugation, surface functionalization, and molecular imaging probe assembly. The azide group provides a robust chemical handle for strain-promoted or CuAAC ligation strategies commonly used in chemical biology and materials research.
1. Biomolecule PEGylation Handles
Azido-PEG6-alcohol is frequently used to introduce a PEG spacer bearing an azide group onto hydroxyl-functional biomolecule derivatives, including PEGylated linkers used in labeling workflows. Researchers and core facilities rely on this reagent to generate clickable conjugation intermediates that can be coupled to cyclooctyne or other alkyne partners for modular assembly of fluorescent tags, affinity handles, and multivalent binding constructs. The PEG6 segment helps maintain colloidal stability and reduces non-specific interactions in complex labeling buffers, while the terminal alcohol supports compatibility with common derivatization strategies used to prepare conjugation-ready materials.
2. Surface And Material Functionalization
Azido-PEG6-alcohol is used to create azide-functional surfaces and polymeric materials for subsequent click-based attachment of dyes, capture ligands, and imaging reagents. Materials scientists often incorporate this reagent into coating, grafting, or post-functionalization pipelines where a hydroxyl-bearing PEG linker improves wetting and surface coverage control before the click step. After azide installation, the reagent enables straightforward coupling to complementary clickable groups to build patterned interfaces, functional films, and sensor-adjacent chemistries without requiring harsh conditions that can damage sensitive substrates.
3. Molecular Imaging Probe Conjugation
Azido-PEG6-alcohol serves as a practical azide-containing linker for preparing molecular imaging reagents and analytical probes that require modular late-stage conjugation. Probe developers use the PEG6 spacer to tune solubility and reduce aggregation tendencies of fluorescent or affinity-based reporters during labeling and purification. By converting a hydroxyl-containing precursor into an azide-bearing intermediate, the reagent supports efficient downstream attachment to alkyne-functional imaging moieties, enabling rapid generation of probe variants for method development in chemical biology and diagnostic reagent research.
4. Diagnostic Reagent Linker Platforms
Azido-PEG6-alcohol is commonly used to build linker platforms for diagnostic and assay reagent development where azide functionality is required for consistent, high-throughput conjugation. Assay developers incorporate PEG-based clickable spacers to improve reagent handling in aqueous assay conditions and to support controlled presentation of signaling or capture components after click coupling. The terminal alcohol and PEG6 flexibility make it suitable for preparing standardized clickable conjugates used in reagent kits, microarray workflows, and automated labeling pipelines that benefit from modular chemistry and reproducible linker architecture.
Computed Properties
| XLogP3 | -0.3 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 8 |
| Rotatable Bond Count | 17 |
| Exact Mass | 307.17433553 g/mol |
| Monoisotopic Mass | 307.17433553 g/mol |
| Topological Polar Surface Area | 80.7Ų |
| Heavy Atom Count | 21 |
| Formal Charge | 0 |
| Complexity | 251 |
| 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 |
Patents
| Publication Number | Title | Priority Date |
|---|---|---|
| WO-2020139807-A2 | Nanocapsules for the delivery of cell modulating agents | 2018-12-23 |
| AU-2019414331-A1 | Nanocapsules for the delivery of cell modulating agents | 2018-12-23 |
| EP-3898978-A2 | Nanocapsules for the delivery of cell modulating agents | 2018-12-23 |
| US-2021322331-A1 | Nanocapsules for the delivery of cell modulating agents | 2018-12-23 |
| CN-113544270-A | Nanocapsules for delivery of cell modulators | 2018-12-23 |
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