Bromo-PEG5-propionic acid is a PEG-based linker bearing a terminal bromo group and a carboxylic acid, providing a chemically addressable handle for controlled conjugation in PROTAC and targeted protein degradation constructs. The ether-rich PEG chain confers conformational flexibility and aqueous solubility, while the bromo substituent enables site-specific functionalization (for example, via nucleophilic substitution or subsequent derivatization to install an appropriate warhead or attachment motif). The terminal propionic acid functionality serves as an acylating or coupling partner, allowing formation of stable amide or ester linkages to connect the linker to ligands or scaffold elements used for recruiting an E3 ligase and the target-binding moiety. In PROTAC design, this linker architecture helps tune the effective distance and orientation between binding partners, which can improve ternary complex formation and degradation efficiency. As a modular PEG spacer, it is valuable for systematic structure–activity studies and for optimizing linker length and chemistry in degradation research.
Structure of 1817735-27-5
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Bromo-PEG5-propionic acid is a PEG-based, bromo-functional linker designed for modular assembly of PROTACs, enabling reliable spatial separation between a ligand and an E3-recruiting or target-binding moiety. Its ether-rich PEG scaffold supports favorable solubility and conformational flexibility, while the bromo group provides a practical handle for controlled bond formation. The following sections describe the linker’s structure and the reactivity options typically used to build PROTAC architectures.
Structure: The linker features a polyethylene glycol chain containing repeating ether units, terminated with a bromo substituent and a propionic acid functionality. It contains C–Br and C–O ether bonds, along with a carboxylic acid capable of hydrogen bonding and ionic interactions. Overall, it is a polar, flexible scaffold.
Reactivity: The bromo terminus is commonly used for nucleophilic substitution or related coupling strategies, where the bromo group serves as a leaving group under appropriate conditions. Carboxylic acid can be activated for amide or ester formation via standard coupling chemistries, often using carbodiimide-based activators and compatible bases. Solvents such as polar aprotic media are frequently employed to promote substitution and minimize side reactions.
* 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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