
m-PEG7-azide | CAS 208987-04-6
| Catalog Number | R14-0171 |
| Category | Azides |
| Molecular Formula | C₁₅H₃₁N₃O₇ |
| Molecular Weight | 365.42 |
* Please be kindly noted products are not for therapeutic use. We do not sell to patients.
Product Introduction
m-PEG7-azide is a polyethylene glycol (PEG)-based PROTAC linker. m-PEG7-azide can be used in the synthesis of a series of PROTACs.
Chemical Information
Product Specification
Application
Computed Properties
Patents
Chemical Information
| Synonyms | mPEG7-N3; azido-mPEG7; 2,5,8,11,14,17,20-Heptaoxadocosane, 22-azido-; 1-azido-2-[2-[2-[2-[2-[2-(2-methoxyethoxy)ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethane; (3,6,9,12,15,18,21-Heptaoxadocosane-1-yl) azide; 22-AZIDO-2,5,8,11,14,17,20-HEPTAOXADOCOSANE |
| Purity | 98% |
| IUPAC Name | 1-azido-2-[2-[2-[2-[2-[2-(2-methoxyethoxy)ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethane |
| SMILES | COCCOCCOCCOCCOCCOCCOCCN=[N+]=[N-] |
| InChI | InChI=1S/C15H31N3O7/c1-19-4-5-21-8-9-23-12-13-25-15-14-24-11-10-22-7-6-20-3-2-17-18-16/h2-15H2,1H3 |
| InChIKey | KKPCQLXBYKYWQE-UHFFFAOYSA-N |
Product Specification
| Storage | Please store the product under the recommended conditions in the Certificate of Analysis. |
Application
m-PEG7-azide is a polyethylene glycol (PEG)-based azide functionalization reagent designed for bioorthogonal click chemistry workflows. As an azide-bearing linker, it is commonly used in strain-promoted or copper-catalyzed azide–alkyne cycloaddition (CuAAC) conjugation strategies to install PEG spacers onto biomolecules, surfaces, and polymeric materials. The presence of a defined PEG chain length supports improved solubility, reduced nonspecific interactions, and tunable hydrophilicity, making m-PEG7-azide a frequent choice in probe preparation, material functionalization, and conjugate library development.
1. PEGylated Biomolecule Conjugates
m-PEG7-azide is widely used to introduce a PEG spacer into biomolecule conjugates where improved aqueous handling and steric shielding are required for downstream labeling or binding assays. Researchers incorporate the azide handle so that biomolecules bearing complementary alkyne partners can be clicked to generate stable PEGylated constructs for protein labeling, peptide modification, and multicomponent reagent assembly. The PEG segment helps maintain colloidal stability during purification and storage, while the azide functionality provides a modular attachment point for subsequent functionalization steps.
2. Surface Functionalization And Coatings
m-PEG7-azide supports azide-based surface engineering for creating hydrophilic, antifouling-like PEG layers on materials used in biosensing and analytical workflows. By coupling m-PEG7-azide onto surfaces that present complementary reactive groups (or by using it as the azide component in click-compatible schemes), laboratories can tune surface wettability and reduce nonspecific adsorption that can otherwise interfere with assay readouts. This application is common in the preparation of microarrays, diagnostic reagent platforms, and functionalized polymer films where consistent PEG presentation is important for reproducible performance.
3. Molecular Imaging Probe Building
m-PEG7-azide is used as a PEG-azide building block in the construction of imaging and detection probes that benefit from improved solubility and reduced aggregation. Probe developers frequently rely on azide–alkyne click-compatible assembly to attach PEG spacers to targeting scaffolds, fluorophores, or reporter constructs, enabling better dispersion in aqueous buffers and more robust handling during conjugate purification. The modular azide handle also facilitates rapid exchange of reporter components, supporting iterative probe optimization in molecular imaging research tool development.
4. Diagnostic Reagent And Assay Platforms
m-PEG7-azide is a practical component for preparing click-assembled diagnostic reagents and assay platform reagents where controlled surface or reagent architecture improves workflow consistency. In many lab and industrial R&D settings, azide-bearing PEG linkers are incorporated to regulate spacing between functional groups, enhance mixing and stability in assay buffers, and minimize nonspecific interactions that can contribute to background signal. The PEGylated azide format is particularly valuable when building multivalent reagent systems, such as modular labeling reagents and conjugate libraries used to screen assay chemistries.
Computed Properties
| XLogP3 | 0.1 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 9 |
| Rotatable Bond Count | 21 |
| Exact Mass | 365.21620034 g/mol |
| Monoisotopic Mass | 365.21620034 g/mol |
| Topological Polar Surface Area | 79Ų |
| Heavy Atom Count | 25 |
| Formal Charge | 0 |
| Complexity | 305 |
| 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-2022122035-A1 | Coagulation factor xia inhibitor, preparation method therefor and use thereof | 2020-12-11 |
| WO-2018211286-A1 | N-type conjugated polymers | 2017-05-19 |
| US-2010143250-A1 | Compounds for the diagnosis of apoptosis | 2007-03-28 |
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