HO-PEG21-OH is a linear, terminally hydroxylated polyethylene glycol linker (PEG) with a long, flexible ethylene glycol chain that provides a hydrophilic spacer between PROTAC components. In targeted protein degradation constructs, such PEG linkers are widely used to tune the effective distance and relative orientation between a ligand that recruits an E3 ubiquitin ligase and a ligand that binds the target protein, thereby improving productive ternary complex formation while reducing non-specific hydrophobic interactions. The two terminal alcohol groups enable straightforward conjugation strategies (for example, through activation to form ethers, esters, or other coupling handles) while maintaining the PEG’s solubility and conformational mobility. This product is valuable for researchers optimizing linker length and physicochemical properties in PROTAC design, supporting systematic structure–activity relationship studies and enhancing experimental reproducibility in degradation assays.
Structure of 928211-42-1
* For research and manufacturing use only. Not for human or clinical use.
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HO-PEG21-OH is a polyethylene glycol-based bifunctional linker designed for constructing PROTACs through reliable, modular conjugation chemistry. Its PEG-rich backbone provides a flexible, hydrophilic spacer that can improve the effective reach and conformational adaptability between the ligand-binding warhead and the E3-recruiting element. This product is commonly used to tune linker length and polarity in targeted protein degradation workflows, and the following points describe its structure and practical reactivity considerations in detail below.
Structure: HO-PEG21-OH is a linear PEG diol featuring terminal hydroxyl groups connected by repeating ether units. The structure is dominated by flexible C–O–C linkages, offering high polarity and strong hydrogen-bonding capacity. As a result, it typically exhibits good solubility in aqueous and mixed organic media and behaves as a hydrophilic spacer.
Reactivity: The terminal alcohols enable PROTAC linker installation via standard hydroxyl-reactive transformations, such as activation to form leaving groups followed by nucleophilic substitution with complementary functional groups on ligands. Common approaches include converting alcohols to activated esters or carbonates, or using coupling strategies compatible with amines or carboxylic acids. Selection of mild bases, appropriate solvents, and temperature control is important to preserve ligand integrity and minimize side reactions during 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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