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  • Dextran sulfate sodium salt from Leuconostoc spp.

  • Dextran sulfate sodium salt from Leuconostoc spp.

    Catalog Number
    ACM9011181
    CAS Number
    9011-18-1
    Product Name
    Dextran sulfate sodium salt from Leuconostoc spp.
    Category
    Natural Polymers and Biopolymers; Polysaccharide
    Description
    DryPowder;Solid
    IUPAC Name
    ethyl 4-aminobenzoate
    Molecular Weight
    165.19g/mol
    Molecular Formula
    C9H11NO2
    Canonical SMILES
    CCOC(=O)C1=CC=C(C=C1)N
    InChI
    InChI=1S/C9H11NO2/c1-2-12-9(11)7-3-5-8(10)6-4-7/h3-6H,2,10H2,1H3
    InChI Key
    BLFLLBZGZJTVJG-UHFFFAOYSA-N
    Boiling Point
    310.0 °C;310 °C
    Melting Point
    92.0 °C;92 °C;92°C
    Solubility
    0.01 M;One gram dissolves in about 5 ml alcohol, 2 ml chloroform, in about 4 ml ether, and in 30 to 50 ml of expressed almond oil or olive oil. Also sol in dil acids.;Soluble in acid;In water, 1,310 mg/L at 25 °C;>24.8 [ug/mL]
    Application
    Dextran sulfate sodium salt derived from Leuconostoc spp. serves a versatile role in scientific research and applications. This white to off-white powder is effectively utilized in a range of electrophoretic techniques, such as polyacrylamide-gel electrophoresis for carbohydrates (C-PAGE) and agarose gel electrophoresis for RNA. It is also incorporated into SPOTs imaging for sequential probing of targets and acts as a component in certain injection buffers. Notably, dextran sulfate sodium salt has been explored for its anticoagulant properties, demonstrating potential as a substitute for heparin, with particular interest in its interactions with enzyme and inhibitor systems within the coagulation cascade. Furthermore, when immobilized on cellulose, it can selectively remove LDL cholesterol during plasmapheresis. Its broad spectrum of biological activities includes enzyme inhibition, immune response modulation, cell interaction influences, and effects on viral infectivity, making it an attractive compound for further scientific inquiry.
    Color/Form
    Rhombohedra from ether;Needles from water
    Complexity
    151
    Covalently-Bonded Unit Count
    1
    EC Number
    202-303-5;618-471-1
    Exact Mass
    165.078979g/mol
    Formal Charge
    0
    Heavy Atom Count
    12
    Log P
    1.86 (LogP);log Kow = 1.86;1.86
    MeSH Entry Terms
    4-Aminobenzoic Acid Ethyl Ester;Acetate, Benzocaine;Americaine;Anaesthesin;Anesthesin;Bensokain;Benzocaine;Benzocaine Acetate;Benzocaine Formate;Benzocaine Hydrobromide;Benzocaine Hydrochloride;Benzocaine Methanesulfonate;Ethoform;Ethyl Aminobenzoate;Formate, Benzocaine;Hydrobromide, Benzocaine;Hydrochloride, Benzocaine;Methanesulfonate, Benzocaine
    Monoisotopic Mass
    165.078979g/mol
    NSC Number
    755909;41531;4688
    Other Experimental
    Stable in air;Henry's Law constant = 1.6X10-8 atm-cu m/mole at 25 °C /Estimated/;Hydroxyl radical reaction rate constant = 3.6X10-11 cu cm/molecule-sec at 25 °C /Estimated/
    Rotatable Bond Count
    3
    RTECS Number
    DG2450000
    Stability
    Stable in air.
    UNII
    U3RSY48JW5
    Vapor Pressure
    2.6X10-4 mm Hg at 25 °C /Estimated/
    XLogP3
    1.9
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