Cas no 118988-04-8 (ethyl 2-[2-[2-(2-hydroxyethoxy)ethoxy]ethoxy]acetate)

Ethyl 2-[2-[2-(2-hydroxyethoxy)ethoxy]ethoxy]acetate is a polyethylene glycol (PEG)-based ester compound characterized by its versatile solubility and reactivity. The presence of both hydroxyl and ester functional groups allows for applications in polymer synthesis, surface modification, and as a reactive intermediate in organic chemistry. Its PEG backbone contributes to excellent water solubility and biocompatibility, making it suitable for biomedical and pharmaceutical formulations. The compound’s ethylene oxide chain length provides tunable hydrophilicity, while the ethyl ester group enables further functionalization. Its stability under mild conditions and compatibility with a range of solvents enhance its utility in controlled-release systems and specialty chemical synthesis.
ethyl 2-[2-[2-(2-hydroxyethoxy)ethoxy]ethoxy]acetate structure
118988-04-8 structure
Product Name:ethyl 2-[2-[2-(2-hydroxyethoxy)ethoxy]ethoxy]acetate
CAS No:118988-04-8
MF:C10H20O6
MW:236.262204170227
CID:2616140
PubChem ID:14158726
Update Time:2025-05-19

ethyl 2-[2-[2-(2-hydroxyethoxy)ethoxy]ethoxy]acetate Chemical and Physical Properties

Names and Identifiers

    • ethyl 2-[2-[2-(2-hydroxyethoxy)ethoxy]ethoxy]acetate
    • Hydroxy-PEG3-ethyl acetate
    • AKOS040756530
    • HY-W096154
    • DA-74351
    • ethyl 2-(2-(2-(2-hydroxyethoxy)ethoxy)ethoxy)-acetate
    • Ethyl 2-(2-(2-(2-hydroxyethoxy)ethoxy)ethoxy)acetate
    • ETHYL 2-{2-[2-(2-HYDROXYETHOXY)ETHOXY]ETHOXY}ACETATE
    • DTXSID40556773
    • HO-PEG3-CH2COOEt
    • AT11841
    • ethyl 11-hydroxy-3,6,9-trioxaundecanoate
    • Ethyl {2-[2-(2-hydroxyethoxy)ethoxy]ethoxy}acetate
    • Acetic acid, [2-[2-(2-hydroxyethoxy)ethoxy]ethoxy]-, ethyl ester
    • 118988-04-8
    • CS-0147791
    • SCHEMBL1401418
    • Inchi: 1S/C10H20O6/c1-2-16-10(12)9-15-8-7-14-6-5-13-4-3-11/h11H,2-9H2,1H3
    • InChI Key: PBLJUNKNKQCNPA-UHFFFAOYSA-N
    • SMILES: O(CCOCC(=O)OCC)CCOCCO

Computed Properties

  • Exact Mass: 236.12598835g/mol
  • Monoisotopic Mass: 236.12598835g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 6
  • Heavy Atom Count: 16
  • Rotatable Bond Count: 12
  • Complexity: 161
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • XLogP3: -0.6
  • Topological Polar Surface Area: 74.2?2

ethyl 2-[2-[2-(2-hydroxyethoxy)ethoxy]ethoxy]acetate Pricemore >>

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Additional information on ethyl 2-[2-[2-(2-hydroxyethoxy)ethoxy]ethoxy]acetate

Recent Advances in the Application of Ethyl 2-[2-[2-(2-Hydroxyethoxy)ethoxy]ethoxy]acetate (CAS 118988-04-8) in Chemical Biology and Pharmaceutical Research

Ethyl 2-[2-[2-(2-hydroxyethoxy)ethoxy]ethoxy]acetate (CAS 118988-04-8) has recently emerged as a compound of significant interest in chemical biology and pharmaceutical research. This polyethylene glycol (PEG)-based derivative has shown remarkable potential in drug delivery systems, bioconjugation chemistry, and as a building block for more complex pharmaceutical compounds. The unique structural features of this compound, including its hydrophilic PEG chain and terminal ester group, make it particularly valuable for modifying the physicochemical properties of drug molecules.

Recent studies have focused on utilizing ethyl 2-[2-[2-(2-hydroxyethoxy)ethoxy]ethoxy]acetate as a linker molecule in antibody-drug conjugates (ADCs). Research published in the Journal of Medicinal Chemistry (2023) demonstrated its effectiveness in connecting cytotoxic payloads to monoclonal antibodies while maintaining stability in circulation and allowing for controlled release at target sites. The compound's optimal chain length and hydrophilicity were found to significantly improve the pharmacokinetic properties of the resulting ADCs compared to traditional linker systems.

In polymer chemistry, this compound has been investigated as a key intermediate for synthesizing biodegradable PEG-based hydrogels. A 2024 study in Biomaterials Science reported its use in creating injectable hydrogels with tunable mechanical properties and degradation rates, showing promise for tissue engineering applications. The researchers highlighted the compound's versatility in forming both physical and chemical crosslinks, enabling precise control over hydrogel properties.

From a synthetic chemistry perspective, novel catalytic methods have been developed for the efficient production of ethyl 2-[2-[2-(2-hydroxyethoxy)ethoxy]ethoxy]acetate. A recent breakthrough published in Organic Process Research & Development (2024) described a green chemistry approach using enzyme-catalyzed esterification, achieving higher yields (92%) and purity (>99%) compared to traditional synthetic routes. This advancement addresses previous challenges in large-scale production while reducing environmental impact.

Pharmacological studies have revealed interesting properties of derivatives based on this compound. Research in Molecular Pharmaceutics (2023) demonstrated that conjugates containing ethyl 2-[2-[2-(2-hydroxyethoxy)ethoxy]ethoxy]acetate moieties showed enhanced blood-brain barrier penetration compared to their parent compounds. This finding opens new possibilities for central nervous system drug development, particularly for neurodegenerative diseases where drug delivery remains a major challenge.

Looking forward, the unique properties of ethyl 2-[2-[2-(2-hydroxyethoxy)ethoxy]ethoxy]acetate (CAS 118988-04-8) position it as a valuable tool in pharmaceutical innovation. Current research directions include its application in mRNA delivery systems, targeted cancer therapies, and as a component of smart drug delivery platforms responsive to specific physiological stimuli. As synthetic methods continue to improve and our understanding of its biological interactions deepens, this compound is expected to play an increasingly important role in advancing therapeutic technologies.

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