Azido-PEG10-azide

 CAS No.: 1421783-42-7  Cat No.: BP-500423  Purity: 98% 4.5  

Azido-PEG10-azide is a bifunctional polyethylene glycol (PEG) linker bearing terminal azide groups, providing a flexible, hydrophilic spacer of intermediate chain length between two conjugation sites. The two azide termini enable efficient bioorthogonal “click” chemistry, most commonly copper-catalyzed or strain-promoted azide–alkyne cycloaddition, allowing researchers to modularly connect a target-binding ligand (e.g., a warhead or receptor-binding moiety) to an E3 ligase recruiter or other functional fragment through orthogonal coupling strategies. In PROTAC and targeted protein degradation workflows, this linker architecture helps tune the effective distance, relative orientation, and conformational freedom of the assembled degrader, which can strongly influence ternary complex formation and degradation potency. Its PEG-based nature also improves aqueous solubility and can reduce nonspecific hydrophobic interactions, supporting more reliable synthesis and characterization of linker–payload conjugates for mechanistic studies.

Azido-PEG10-azide

Structure of 1421783-42-7

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Category
PROTAC Linker
Molecular Formula
C₂₂H₄₄N₆O₁₀
Molecular Weight
552.62

* For research and manufacturing use only. Not for human or clinical use.

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Purity
98%
Storage
Please store the product under the recommended conditions in the Certificate of Analysis.
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Room temperature in continental US; may vary elsewhere.
IUPACName
1-azido-2-[2-[2-[2-[2-[2-[2-[2-[2-[2-(2-azidoethoxy)ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethane
Synonyms
1,32-diazido-3,6,9,12,15,18,21,24,27,30-decaoxadotriacontane
InChI Key
NLHKJEYZBGTRDB-UHFFFAOYSA-N
InChI
InChI=1S/C22H44N6O10/c23-27-25-1-3-29-5-7-31-9-11-33-13-15-35-17-19-37-21-22-38-20-18-36-16-14-34-12-10-32-8-6-30-4-2-26-28-24/h1-22H2
SMILES
C(COCCOCCOCCOCCOCCOCCOCCOCCOCCOCCN=[N+]=[N-])N=[N+]=[N-]

Azido-PEG10-azide is a bifunctional polyethylene glycol (PEG) linker designed for modular construction of PROTACs and other targeted degradation conjugates. Its two terminal azide groups enable orthogonal conjugation strategies that support efficient assembly of ligand–linker–ligand architectures while improving aqueous solubility and reducing nonspecific interactions. The linker’s flexible PEG backbone provides conformational mobility, which can help maintain productive binding and promote formation of the ternary complex. Detailed structural and reactivity considerations are provided below.

Structure: The molecule is a PEG-based linker bearing two terminal azide functional groups, connected through ether linkages along a flexible polyether chain. The azides are stable under many storage conditions yet serve as reactive handles for click-type conjugation. Overall, the PEG segment imparts hydrophilicity and favorable solubility in aqueous media.

Reactivity: Azido-PEG-azide is well suited for copper-catalyzed azide–alkyne cycloaddition and related azide click reactions, where azide groups react with terminal alkynes to form stable triazole linkages. Typical protocols employ a Cu(I) source and a suitable reducing agent, often in mixed aqueous/organic solvents, to generate the active catalytic species in situ. Reaction efficiency depends on ligand accessibility and maintaining conditions compatible with sensitive targeting ligands.

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* 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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Tip: Chemical formula is case sensitive. C22H30N4O c22h30n40
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