Amino-PEG7-alcohol is a polyethylene glycol (PEG) based bifunctional linker featuring a terminal primary amine and a terminal hydroxyl group, providing a flexible, water-soluble chain of intermediate length suitable for bioconjugation workflows. The amine enables covalent attachment to PROTAC-relevant warheads or handles (for example, via amide coupling, carbamate formation, or reductive amination), while the alcohol can serve as an additional functional group for further derivatization or for constructing controlled attachment geometries. In PROTAC design, such PEG linkers help tune the effective distance and relative orientation between the ligand-binding domain and the E3 ligase recruiting module, often improving solubility and reducing nonproductive aggregation, thereby supporting productive ternary complex formation. This linker is valuable for researchers optimizing linker length, flexibility, and physicochemical properties across targeted protein degradation series, enabling systematic structure–property studies and facilitating downstream conjugation to diverse chemical scaffolds.
Structure of 1425973-14-3
* For research and manufacturing use only. Not for human or clinical use.
| Size | Price | Stock | Quantity |
|---|---|---|---|
| -- | $-- | In stock |
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| ConcentrationVolumeMass | 1 mg | 5 mg | 10 mg |
|---|---|---|---|
| 1 mM | 3.0731 mL | 15.3657 mL | 30.7314 mL |
| 5 mM | 0.6146 mL | 3.0731 mL | 6.1463 mL |
| 10 mM | 0.3073 mL | 1.5366 mL | 3.0731 mL |
Amino-PEG7-alcohol is a polyethylene glycol-based linker building block designed to support PROTAC assembly by providing a flexible, hydrophilic spacer and a functional handle for conjugation. Its ether-rich backbone helps tune solubility and conformational freedom between the target-binding ligand and the E3-recruiting moiety, which can improve productive ternary complex formation. Detailed structural and reactivity guidance is provided below.
Structure: The linker contains an amino functional group and a terminal alcohol, connected through a PEG chain composed of repeating ether units. This architecture provides flexible C–O and C–C connectivity, with multiple ether oxygen atoms that support hydrogen-bonding and enhanced polarity.
Reactivity: The amino group is suitable for nucleophilic coupling strategies such as amide bond formation with activated carboxylic acids, or for carbamate formation using activated carbonyl derivatives. The terminal alcohol can participate in esterification or ether-forming reactions under standard coupling conditions. Typical approaches use coupling reagents and base in polar aprotic solvents, with reaction progress monitored by chromatographic methods to ensure clean functionalization.
* 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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