BDP FL-PEG5-azide is a bifunctional PEG-based linker bearing a terminal azide group suitable for copper-free or copper-catalyzed azide–alkyne cycloaddition (click) chemistry and incorporating a fluorescent BDP (boron-dipyrromethene) reporting handle. Structurally, it consists of a short, flexible oligo(ethylene glycol) chain that provides aqueous solubility and spatial separation between conjugated partners, while the azide enables site-specific attachment to alkyne-functional ligands or PROTAC components. In targeted protein degradation workflows, such linkers are used to connect a recognition element (e.g., a ligand for an E3 ligase) to a second binding module or to install a fluorescent tag for monitoring synthesis, cellular uptake, and intracellular trafficking. The BDP fluorophore allows researchers to track conjugate integrity and localization during optimization of linker length and attachment geometry, improving the experimental design of PROTACs and related degraders.
Structure of 2093197-91-0
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BDP FL-PEG5-azide is a polyethylene glycol (PEG)-based linker engineered for PROTAC assembly, providing a flexible spacer that can improve productive ternary complex formation between a target-binding ligand and an E3 ligase recruiter. Its azide handle enables reliable bioorthogonal conjugation strategies commonly used in targeted protein degradation workflows. The following sections describe the molecule’s structure-related features and practical reactivity considerations for constructing PROTACs in a research setting.
Structure: The linker comprises a PEG chain featuring ether linkages that impart conformational flexibility and hydrophilicity, coupled to a terminal azide functional group. This combination supports solubility and spacer behavior, while the azide provides a chemically distinct reaction site for downstream conjugation.
Reactivity: The terminal azide is well suited for azide-based click conjugation, particularly strain-promoted azide–alkyne cycloaddition or copper-catalyzed azide–alkyne cycloaddition, depending on the partner functionality. Typical PROTAC synthesis uses inert atmosphere when required, polar aprotic solvents for solubility, and controlled temperatures to preserve sensitive ligands. Reaction proceeds via cycloaddition to form a stable triazole linkage under standard click-chemistry principles.
* 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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