Benzyl-PEG7-azide is a polyethylene glycol (PEG) linker bearing a benzyl group at one terminus and an azide handle at the other, providing a flexible, water-compatible chain length suitable for bioconjugation workflows. The PEG segment acts as a spacer that can reduce steric interference between a PROTAC’s binding modules, improve effective reach, and often enhance solubility in aqueous assay conditions. In targeted protein degradation design, the azide functionality enables site-specific attachment to complementary alkyne-bearing partners via copper-catalyzed or strain-promoted azide–alkyne cycloaddition, allowing researchers to assemble PROTAC constructs with controlled linker placement. This linker is particularly valuable for generating modular degradation libraries where tuning of spatial orientation and linker length is critical for maintaining ternary complex formation and degradation potency.
Structure of 868594-42-7
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Benzyl-PEG7-azide is a PEG-based azide linker designed for modular PROTAC synthesis, enabling efficient conjugation of ligands through azide-compatible chemistries. Its flexible poly(ethylene glycol) scaffold supports favorable linker solvation and conformational freedom, which can help tune ternary complex formation and targeted protein degradation performance. The benzyl capping group provides a defined attachment handle, while the azide functionality enables reliable coupling strategies.
Structure: The molecule contains a benzyl-terminated PEG chain bearing a terminal azide group. It features ether linkages characteristic of PEG, flexible C–O and C–C connectivity, and a covalently bound azide suitable for click-type transformations. The resulting amphiphilic character supports aqueous solubility and reduced nonspecific hydrophobic interactions.
Reactivity: The azide group is well suited for copper-catalyzed azide–alkyne cycloaddition and related azide coupling approaches used in PROTAC assembly. Typical conditions employ a compatible alkyne partner, a copper catalyst system, and an inert or controlled atmosphere to minimize side reactions; aqueous/organic mixed solvents are commonly used for solubility. Reaction progress is governed by catalyst activation and alkyne accessibility, with purification by standard chromatography or precipitation methods.
* 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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