m-PEG20-alcohol is a monodisperse, methoxy-terminated polyethylene glycol (PEG) linker bearing a terminal primary alcohol, designed for modular conjugation in targeted protein degradation constructs. Structurally, it comprises an ether-linked PEG chain of extended length that provides conformational flexibility and hydrophilicity, while the terminal alcohol serves as a reactive handle for coupling to electrophilic warheads or to complementary linker fragments (for example, via esterification, etherification, or activation to form further intermediates). In PROTAC design, PEG linkers commonly help tune the effective distance and orientation between the binding moieties, reduce nonspecific hydrophobic interactions, and improve solubility and handling of multicomponent degraders. The “m-” substitution pattern supports consistent linker geometry, facilitating reproducible synthesis and characterization. This product is therefore valuable for researchers optimizing linker length, attachment chemistry, and overall physicochemical properties to enhance degradation efficiency and experimental robustness.
Structure of 1059605-06-9
* For research and manufacturing use only. Not for human or clinical use.
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m-PEG20-alcohol is a polyethylene glycol-based linker alcohol designed to support the modular synthesis of PROTACs by providing a flexible, hydrophilic spacer between binding elements. Its ether-rich PEG backbone can enhance solubility and reduce nonspecific interactions, while the terminal alcohol enables straightforward functionalization for conjugation strategies. The subsequent points describe its structural features and practical considerations for assembling PROTAC constructs using this linker.
Structure: The linker comprises a repeating PEG ether chain terminated by a primary alcohol. Its polyether backbone contains multiple ether oxygen atoms, enabling strong hydrogen-bonding interactions and high conformational flexibility. The molecule is generally characterized by hydrophilicity and ether-dominated polarity, supporting improved aqueous compatibility.
Reactivity: As a terminal alcohol, it is suitable for conversion into activated derivatives (for example, ester or carbonate intermediates) that can be coupled to complementary PROTAC fragments bearing nucleophiles such as amines or carboxylates. Typical transformations rely on standard alcohol activation chemistries using coupling reagents under mild, anhydrous conditions with inert atmosphere when required. Solvent choice often favors polar aprotic media to maintain solubility and reaction efficiency.
* 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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