Amino-PEG5-alcohol is a bifunctional polyethylene glycol linker featuring a terminal primary amine and a terminal hydroxyl group, providing a flexible, hydrophilic chain of five ethylene glycol units. The ether-rich PEG backbone confers conformational mobility and improves aqueous solubility, while the amine and alcohol termini serve as orthogonal handles for chemical conjugation. In PROTAC and targeted protein degradation workflows, such linkers are used to spatially separate the ligand-binding warhead from the E3 ligase–recruiting moiety, tuning effective intramolecular geometry and thereby influencing ternary complex formation and degradation potency. The PEG segment can also reduce non-specific hydrophobic interactions and help maintain solubility of larger conjugates during synthesis and biological testing. This linker is therefore valuable for constructing modular PROTACs, enabling systematic optimization of linker length and attachment chemistry to support reproducible, structure–function studies in targeted degradation research.
Structure of 34188-11-9
* For research and manufacturing use only. Not for human or clinical use.
| Size | Price | Stock | Quantity |
|---|---|---|---|
| -- | $-- | In stock |
Looking for different specifications? Click to request a custom quote!
Capabilities & Facilities
Popular Publications Citing BOC Sciences Products
| ConcentrationVolumeMass | 1 mg | 5 mg | 10 mg |
|---|---|---|---|
| 1 mM | 4.2143 mL | 21.0713 mL | 42.1425 mL |
| 5 mM | 0.8429 mL | 4.2143 mL | 8.4285 mL |
| 10 mM | 0.4214 mL | 2.1071 mL | 4.2143 mL |
Amino-PEG5-alcohol is a PEG-based bifunctional linker designed for modular assembly in targeted protein degradation (PROTAC) workflows. Its flexible polyether backbone supports productive ternary complex formation, while the terminal amino and alcohol functionalities enable robust conjugation to ligands under standard bioconjugation and coupling strategies. This linker is well suited for constructing PROTACs where controlled spacing and aqueous compatibility are important, and the following sections describe its structure and practical reactivity for experimental use.
Structure: The linker comprises a flexible polyethylene glycol chain terminated by an amino group and a primary alcohol. It contains repeating ether linkages that confer conformational mobility and hydrophilicity, alongside a carbon–oxygen bond at the alcohol terminus. The amino functionality provides a reactive handle for amide or carbamate formation.
Reactivity: The amino group can be employed in amide coupling (via activated carboxylic acids) or carbamate formation (via activated carbonyl derivatives), while the alcohol can participate in esterification or conversion to leaving-group derivatives for subsequent substitution. Typical conditions use coupling reagents such as carbodiimides or activated chloroformates, with polar aprotic solvents and base to promote nucleophilic acyl substitution. Protecting-group strategies are often used to maintain chemoselectivity during stepwise PROTAC synthesis.
* 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
Please contact us with any specific requirements and we will get back to you as soon as possible.