mPEG10-alcohol is a methoxy-terminated poly(ethylene glycol) monomethyl ether with an alcohol end group, providing a short, flexible PEG chain suitable for controlled linker construction. Structurally, it is characterized by a linear ethylene glycol repeat segment capped at one terminus by a methyl ether and at the other by a primary hydroxyl, enabling straightforward functionalization via standard PEG chemistry (e.g., conversion of the alcohol to activated esters, carbonates, or other coupling handles). In PROTAC and targeted protein degradation workflows, such PEG linkers are commonly used to tune solubility, reduce nonspecific adsorption, and modulate the effective distance and conformational freedom between a ligand for an E3 ligase and a target-binding moiety. The PEG spacer can thereby improve aqueous handling and help preserve productive ternary-complex formation. As a modular building block, mPEG10-alcohol supports the synthesis of degraders and related conjugates where balanced hydrophilicity and linker flexibility are critical for experimental performance.
Structure of 27425-92-9
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mPEG10-alcohol is a polyethylene glycol (mPEG)–derived alcohol linker designed to support PROTAC construction by enabling controlled conjugation, solubility enhancement, and improved handling of bifunctional degradation agents. Its ether-rich, flexible scaffold can help tune physicochemical properties and facilitate attachment to ligands or reactive handles under standard bioconjugation workflows. The detailed structural and reactivity considerations are provided below to guide experimental design.
Structure: mPEG10-alcohol comprises a methoxy-capped poly(ethylene glycol) chain terminating in a primary alcohol. The molecule features repeating ether linkages that confer conformational flexibility, hydrophilicity, and chemical stability, while the terminal hydroxyl provides a reactive functional group for derivatization. These characteristics make it suitable for linker-mediated conjugation.
Reactivity: The terminal alcohol enables common PROTAC-compatible coupling strategies after conversion to activated intermediates, such as ester or carbonate derivatives, or via nucleophilic substitution routes to introduce electrophilic sites for ligand attachment. Typical conditions use polar aprotic or aqueous-compatible solvents and mild bases or coupling reagents, with reaction temperatures selected to preserve sensitive ligands. Mechanistically, formation of an activated carbonyl or leaving group allows controlled nucleophilic attack by target functional groups, yielding stable linkages suitable for bifunctional assembly.
* Our calculator is based on the following equation:
Concentration (start) x Volume (start) = Concentration (final) x Volume (final)
It is commonly abbreviated as: C1V1 = C2V2
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