m-PEG5-triethoxysilane

 CAS No.: 2243566-42-7  Cat No.: BP-500650 4.5  

m-PEG5-triethoxysilane is a heterobifunctional PEG-based linker featuring a methoxy-terminated PEG chain on the PEG chain and a terminal triethoxysilane group. The triethoxysilane moiety hydrolyzes and condenses to form stable siloxane bonds with hydroxylated inorganic surfaces (e.g., glass, silica, or oxidized metal oxides), enabling robust surface immobilization or incorporation into silica-based linkers. In PROTAC and targeted degradation workflows, such PEG linkers are commonly used to introduce a flexible hydrophilic spacer that can reduce non-specific interactions, improve solubility, and provide controlled distance between a targeting ligand and an E3 ligase-binding module when conjugated to surface- or matrix-associated components. Its PEG5 chain length offers a balance between mobility and effective reach, supporting reproducible conjugation chemistry and facilitating downstream assembly of degraders or immobilized degradation assays.

m-PEG5-triethoxysilane

Structure of 2243566-42-7

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PROTAC Linker
Molecular Formula
C₂₁H₄₅NO₉Si
Molecular Weight
483.67

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

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Please store the product under the recommended conditions in the Certificate of Analysis.
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IUPACName
3-[2-[2-[2-(2-methoxyethoxy)ethoxy]ethoxy]ethoxy]-N-(3-triethoxysilylpropyl)propanamide
InChI Key
RXDVHXFXNJERJZ-UHFFFAOYSA-N
InChI
InChI=1S/C21H45NO9Si/c1-5-29-32(30-6-2,31-7-3)20-8-10-22-21(23)9-11-25-14-15-27-18-19-28-17-16-26-13-12-24-4/h5-20H2,1-4H3,(H,22,23)
SMILES
CCO[Si](CCCNC(=O)CCOCCOCCOCCOCCOC)(OCC)OCC

m-PEG5-triethoxysilane is a versatile PEG-based linker designed to connect PROTAC scaffolds to silane-functional surfaces or materials while maintaining hydrophilicity and flexible spacing. Its triethoxysilane group enables robust surface anchoring through hydrolysis and condensation, supporting stable immobilization strategies that can improve local concentration and reproducibility in targeted protein degradation workflows. The detailed structure and reactivity considerations for PROTAC assembly and conjugation are provided below.

Structure: The molecule combines a meta-substituted PEG chain with a triethoxysilane functionality. It contains ether linkages within the PEG segment, and an organosilane moiety bearing three alkoxy groups. The overall structure is flexible, polar, and suitable for aqueous-compatible conjugation chemistry.

Reactivity: The triethoxysilane portion undergoes hydrolysis to form silanol intermediates, followed by condensation to generate Si–O–Si linkages. Typical PROTAC-related conjugation or surface immobilization uses controlled moisture, mild acid or base to tune hydrolysis rate, and polar solvents such as alcohol/water mixtures. No metal catalysts are generally required; reaction proceeds via sol–gel principles under conditions that promote stable siloxane network formation.

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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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