Bis-PEG15-acid is a bifunctional polyethylene glycol (PEG) linker featuring two PEG arms terminated with carboxylic acid groups, providing a long, hydrophilic spacer suitable for constructing PROTACs and related targeted protein degradation conjugates. Structurally, the extended PEG chain length and flexible ether backbone reduce steric constraints and improve aqueous solubility, while the terminal carboxylates enable robust amide-bond formation or other standard coupling chemistries to attach ligands or reactive handles. In PROTAC design, such a bis-functional PEG linker can spatially separate an E3 ligase–binding moiety from a target-binding ligand, thereby tuning effective ternary complex formation and promoting productive ubiquitination. Its value for targeted degradation research lies in its ability to systematically modulate linker length and geometry, facilitating optimization of degradation potency, selectivity, and physicochemical properties during iterative synthesis and biological evaluation.
* For research and manufacturing use only. Not for human or clinical use.
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Bis-PEG15-acid, is a polyethylene glycol-based bifunctional acid designed to connect two ligating fragments while providing conformational flexibility and improved aqueous compatibility. Its PEG-rich architecture can help maintain productive geometry for ternary complex formation and reduce non-specific interactions. The molecule is intended for researchers constructing targeted protein degradation (PROTAC) conjugates, and the following points describe its structure and practical reactivity considerations in PROTAC synthesis.
Structure: Bis-PEG15-acid is a PEG-based bis-functional linker featuring ether-rich polymer segments and terminal carboxylic acid functionality. The structure contains multiple C–O and C–C connections within the PEG backbone, offering high polarity and water solubility, with an acid group suitable for coupling chemistry.
Reactivity: The carboxylic acid termini enable standard PROTAC linker coupling to amine- or alcohol-containing warheads via amide or ester-forming activation. Typical approaches include converting the acid to an activated ester or using carbodiimide-mediated coupling under mild, aqueous or mixed-solvent conditions, often with base and coupling reagents. PEG linkers generally tolerate common organic solvents and do not require specialized catalysts beyond those used for amide/ester bond formation.
* 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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