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  • Trimethylolpropane tris(3-mercaptopropionate)

  • Trimethylolpropane tris(3-mercaptopropionate)

    Catalog Number
    ACM33007839
    CAS Number
    33007-83-9
    Product Name
    Trimethylolpropane tris(3-mercaptopropionate)
    Structure
    Category
    Monomers
    Synonyms
    opanediylester;propanoicacid,3-mercapto-,2-ethyl-2-[(3-mercapto-1-oxopropoxy)methyl]-1,3-pr;PROPANOIC ACID, 3-MERCAPTO-, 2-ETHYL-2- [(3-MERCAPTO-1-OXOPROPOXY) METHYL]-1, 3-PROPANEDIYL ESTER;TRIMETHYLOLPROPANE TRI(3-MERCAPTO PROPIONATE);TRIMETHYLOLPROPANE
    IUPAC Name
    2,2-bis(3-sulfanylpropanoyloxymethyl)butyl 3-sulfanylpropanoate
    Molecular Weight
    398.6g/mol
    Molecular Formula
    C15H26O6S3
    Canonical SMILES
    CCC(COC(=O)CCS)(COC(=O)CCS)COC(=O)CCS
    InChI
    InChI=1S/C15H26O6S3/c1-2-15(9-19-12(16)3-6-22,10-20-13(17)4-7-23)11-21-14(18)5-8-24/h22-24H,2-11H2,1H3
    InChI Key
    IMQFZQVZKBIPCQ-UHFFFAOYSA-N
    Application
    Trimethylolpropane tris(3-mercaptopropionate) serves a versatile role as a cross-linking and modifying agent, instrumental in the development of various advanced materials and applications. This colorless to light yellow liquid is primarily used to create hydrogels by crosslinking inulin derivatives, which are essential for various scientific studies due to their unique properties. It also plays a significant role in constructing porous hybrid monolithic materials, providing structure and stability needed in multiple fields. Furthermore, it acts as a monomer in the synthesis of thiol-ene-based polymeric fluorescence sensors through photo-initiated polymerization, leading to innovative advancements in sensor technology. Its ability to dissolve in water and polar solvents enhances its functionality across diverse applications, making it a critical component in the formulation of specialized polymers, resins, and coatings. Additionally, its use as a photoinitiator for UV-reactive coatings and inks demonstrates its importance in surface treatment and printing technologies. Beyond these applications, it functions as a chelating agent to tackle heavy metal toxicity and modifies emulsions for the effective extraction of heavy metals from water, underscoring its significance in environmental remediation efforts.
    Complexity
    348
    Covalently-Bonded Unit Count
    1
    EC Number
    251-336-1
    Exact Mass
    398.089152g/mol
    Formal Charge
    0
    Heavy Atom Count
    24
    Monoisotopic Mass
    398.089152g/mol
    Rotatable Bond Count
    16
    UNII
    BYN53W5D3L
    XLogP3
    1.6
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