Amino-PEG10-alcohol is an amino-terminated polyethylene glycol linker bearing a terminal primary alcohol, providing a flexible, hydrophilic chain that typically spans roughly ten ethylene glycol units. The linker’s ether-rich backbone imparts conformational mobility and aqueous solubility, while the terminal amine enables straightforward conjugation to PROTAC warheads or ligands via amide coupling, carbamate formation, or reductive amination strategies, and the alcohol functionality can be used for derivatization when an additional handle is required. In PROTAC design, PEG linkers are widely used to spatially separate binding motifs, reduce steric interference, and promote productive ternary complex formation by allowing the recruited target-binding and E3-ligase-binding components to adopt favorable relative orientations. This material is valuable for systematic linker-length and attachment-position optimization in targeted protein degradation studies, helping researchers tune degradation potency and selectivity while maintaining solubility and minimizing nonspecific aggregation.
Structure of 129449-09-8
* For research and manufacturing use only. Not for human or clinical use.
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Amino-PEG10-alcohol, provides a hydrophilic, flexible polyethylene glycol (PEG) spacer terminating in a primary amino group and a hydroxyl handle. Such dual functionality enables modular conjugation to targeting ligands and E3-recruiting moieties, supporting efficient assembly of degraders with improved solubility and reduced nonspecific interactions. The detailed structural and reactivity characteristics are provided below.
Structure: Amino-PEG10-alcohol is a PEG-based linker featuring repeating ether units that confer conformational flexibility, along with a terminal primary amino group and an alcohol. Its structure contains ether linkages and aliphatic C–N and C–O bonds, typically yielding a water-compatible, polar, and hydrogen-bonding capable scaffold.
Reactivity: The terminal amino group is suited for nucleophilic acyl substitution or coupling reactions to install activated carboxylates or carboxylic acid derivatives, while the alcohol can participate in esterification or ether-forming transformations under standard organic synthesis conditions. Common approaches include amide or carbamate bond formation using coupling reagents, with polar aprotic solvents and mild bases to preserve PEG integrity. Reaction design should consider PEG’s solubility and steric accessibility to maintain efficient 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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