Tetraethylene glycol monoethyl ether is a polyethylene glycol–type linker featuring an ether-terminated chain with a terminal ethyl substituent, providing a flexible, hydrophilic segment suitable for conjugation in bifunctional constructs. In PROTAC and targeted protein degradation designs, such PEG-derived linkers help tune the spatial relationship between the ligand that recruits the E3 ubiquitin ligase and the ligand that binds the target protein, thereby influencing productive ternary complex formation and overall degradation potency. The repeating ethylene glycol units can reduce nonspecific hydrophobic interactions, improve aqueous solubility, and accommodate conformational freedom, which is often critical for optimizing linker length and geometry in degradation assays. As a research-grade building block, it supports systematic linker engineering, enabling investigators to evaluate how hydrophilicity and chain flexibility affect intracellular stability, cell permeability trends, and the efficiency of ubiquitination-driven target turnover.
Structure of 5650-20-4
* For research and manufacturing use only. Not for human or clinical use.
| Size | Price | Stock | Quantity |
|---|---|---|---|
| 100 mg | $439 | In stock | |
| 500 mg | $524 | In stock |
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tetraethylene glycol monoethyl ether, provides a flexible, hydrophilic spacer that can modulate linker length, solvation, and conformational freedom between an E3 ligase ligand and a target-binding moiety. Its ether-rich architecture supports favorable aqueous compatibility and can help tune intramolecular positioning to improve productive ternary complex formation. The detailed structural and synthetic considerations are provided below to support experimental PROTAC construction and optimization.
Structure: The linker is composed of an ethylene glycol oligomer bearing a terminal ethyl ether, featuring multiple ether oxygen atoms. It contains repeating C–O–C ether linkages that confer conformational flexibility and strong hydrogen-bond acceptor character, typically resulting in good water miscibility and low polarity-driven aggregation.
Reactivity: As an ether-based, non-activated spacer, it is generally used by functionalizing either terminus to enable coupling to PROTAC warheads and E3 ligase ligands. Suitable strategies include standard nucleophilic substitution or ether/ester-forming reactions after introducing complementary reactive groups on the linker. Reactions are commonly performed under inert or controlled conditions in polar aprotic solvents, using appropriate bases or coupling reagents consistent with the functional groups present on partner ligands.
Dear team. How to prepare Tetraethylene glycol monoethyl ether in lab ?
Tetraethylene glycol monoethyl ether is produced through the reaction of ethylene oxide with diethylene glycol. This process involves the addition of four ethylene oxide molecules to one diethylene glycol molecule.
12/7/2018
Hi! What is the environmental Impact of Tetraethylene glycol monoethyl ether ?
Tetraethylene glycol monoethyl ether is biodegradable, which means it can break down in the environment over time.
25/6/2020
What is the role of Tetraethylene glycol monoethyl ether in solvent industry ?
Good evening! Tetraethylene glycol monoethyl ether is primarily used as a solvent in various applications, including paints, coatings, inks, and cleaning products. It helps dissolve and disperse other substances and is often preferred due to its low volatility and stability.
29/3/2021
synthesize other compounds
We buy Tetraethylene glycol monoethyl ether and use it to synthesize other compounds, which has a high yield.
19/2/2016
synthesize PROTAC
Tetraethylene glycol monomethyl ether is a PEG-based PROTAC linker, so we use it in the synthesis of PROTACs. The effect expected was seen with it!
11/7/2018
stabilize emulsions
Satisfied with product. In water-based formulations, we use Tetraethylene glycol monoethyl ether to facilitate the mixing and compatibility of different components. It can stabilize emulsions and improve the performance of various formulations.
12/1/2022
* 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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