Hydroxy-PEG11-Boc
Hydroxy-PEG11-Boc is a heterobifunctional polyethylene glycol (PEG) linker featuring a terminal hydroxyl group and a tert-butyl ester-protected carboxyl group, providing a hydrophilic, flexible spacer for PROTAC synthesis. The PEG chain length of approximately eleven ethylene glycol units imparts conformational mobility and aqueous solubility, while the tert-butyl ester protects a carboxyl group and can be cleaved under acidic conditions to reveal the carboxylic acid for downstream coupling. In PROTAC design, such PEG-based linkers help position the E3-ligase-binding ligand and the target-binding warhead at an appropriate distance and orientation, reducing steric clashes and improving productive ternary complex formation. The hydroxyl/tert-butyl ester functionality supports stepwise conjugation strategies, facilitating reproducible assembly of degraders and optimization of linker length and polarity. This product is valuable for researchers seeking robust, water-compatible linker scaffolds to systematically tune degradation potency and selectivity in targeted protein degradation studies.
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* For research and manufacturing use only. Not for human or clinical use.
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Hydroxy-PEG11-Boc is a polyethylene glycol (PEG)-based linker designed for assembling PROTACs and other targeted protein degradation constructs. Its PEG segment provides conformational flexibility and improved solubility, while the Boc-protected functionality enables controlled downstream coupling to ligands under standard synthetic workflows. The hydroxyl handle supports reliable functionalization strategies, and the resulting linker architecture is well suited for tuning spatial separation between binding elements. Detailed structural and reactivity considerations are provided below.
Structure: The linker comprises a PEG chain terminated with a hydroxyl group and bearing a Boc-protected functional site. It contains repeating ether linkages typical of PEG, providing a flexible, hydrophilic scaffold. The Boc group is a carbamate protecting group that can be removed under acidic conditions, enabling chemoselective activation.
Reactivity: Boc functionality is commonly deprotected using mild acid conditions to reveal the corresponding amine or reactive carbamate-derived intermediate, which can then be used for PROTAC assembly. The hydroxyl terminus can be converted to activated derivatives (for example, via standard leaving-group formation) for nucleophilic substitution or coupling to electrophilic partners. Solvent systems and catalysts are selected to preserve PEG integrity and avoid side reactions during linker-ligand conjugation.
* 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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