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  • Chitosan (200-600mPa·s, 0.5% in 0.5% Acetic Acid at 20°C)

  • Chitosan (200-600mPa·s, 0.5% in 0.5% Acetic Acid at 20°C)

    Catalog Number
    ACM9012764-3
    CAS Number
    9012-76-4
    Product Name
    Chitosan (200-600mPa·s, 0.5% in 0.5% Acetic Acid at 20°C)
    Category
    Polymers
    Description
    Solid
    IUPAC Name
    methyl N-[(2S,3R,4R,5S,6R)-5-[(2S,3R,4R,5S,6R)-3-amino-5-[(2S,3R,4R,5S,6R)-3-amino-5-[(2S,3R,4R,5S,6R)-3-amino-5-[(2S,3R,4R,5S,6R)-3-amino-5-[(2S,3R,4R,5S,6R)-3-amino-5-[(2S,3R,4R,5S,6R)-3-amino-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4-hydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4-hydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4-hydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4-hydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4-hydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2-[(2R,3S,4R,5R,6S)-5-amino-6-[(2R,3S,4R,5R,6R)-5-amino-4,6-dihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy-4-hydroxy-2-(hydroxymethyl)oxan-3-yl]oxy-4-hydroxy-6-(hydroxymethyl)oxan-3-yl]carbamate
    Molecular Weight
    1526.5g/mol
    Molecular Formula
    C56H103N9O39
    Canonical SMILES
    COC(=O)NC1C(C(C(OC1OC2C(OC(C(C2O)N)OC3C(OC(C(C3O)N)O)CO)CO)CO)OC4C(C(C(C(O4)CO)OC5C(C(C(C(O5)CO)OC6C(C(C(C(O6)CO)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)CO)OC9C(C(C(C(O9)CO)O)O)N)O)N)O)N)O)N)O)N)O)N)O
    InChI
    InChI=1S/C56H103N9O39/c1-87-56(86)65-28-38(84)46(19(10-74)96-55(28)104-45-18(9-73)95-49(27(64)37(45)83)97-39-12(3-67)88-47(85)20(57)31(39)77)103-54-26(63)36(82)44(17(8-72)94-54)102-53-25(62)35(81)43(16(7-71)93-53)101-52-24(61)34(80)42(15(6-70)92-52)100-51-23(60)33(79)41(14(5-69)91-51)99-50-22(59)32(78)40(13(4-68)90-50)98-48-21(58)30(76)29(75)11(2-66)89-48/h11-55,66-85H,2-10,57-64H2,1H3,(H,65,86)/t11-,12-,13-,14-,15-,16-,17-,18-,19-,20-,21-,22-,23-,24-,25-,26-,27-,28-,29-,30-,31-,32-,33-,34-,35-,36-,37-,38-,39-,40-,41-,42-,43-,44-,45-,46-,47-,48+,49+,50+,51+,52+,53+,54+,55+/m1/s1
    InChI Key
    FLASNYPZGWUPSU-SICDJOISSA-N
    Application
    Chitosan (200-600mPa·s, 0.5% in 0.5% Acetic Acid at 20°C) serves as a versatile and effective ingredient valued for its various beneficial properties in cosmetics and pharmaceuticals. This film-forming polysaccharide is odorless and appears as either a white or creamy-white powder, sometimes looking 'cotton-like' during fiber formation. It enhances skin moisture retention by preventing transepidermal water loss and can bind other ingredients to increase their availability to the skin, such as improving liposome stability. Known for its antibacterial properties, chitosan also contributes to the microbiological stability of preparations. Studies show it can boost the water resistance of sunscreens and prolong the scent longevity in fragrances. Acting as a skin conditioner, chitosan improves skin softness and is commonly found in moisturizers, sunscreens, acne treatments, and hair care products. Derived from shrimp shells, it is a cationic polymer prepared through the deacetylation of chitin. This enhances its biodegradability, biocompatibility, and antibacterial activity, making it suitable for numerous applications. In pharmaceuticals, chitosan is used in various drug delivery systems, including controlled drug delivery, mucoadhesive dosage forms, and gene delivery, processed into gels, films, beads, microspheres, tablets, and liposome coatings through techniques like spray-drying and granulation.
    Complexity
    2630
    Covalently-Bonded Unit Count
    1
    EC Number
    618-480-0
    Exact Mass
    1525.635315g/mol
    Formal Charge
    0
    Heavy Atom Count
    104
    MeSH Entry Terms
    Chitosan;Poliglusam
    Monoisotopic Mass
    1525.635315g/mol
    Rotatable Bond Count
    27
    XLogP3
    -21.4
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