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KLEPTOSE®

hydroxypropyl-betacyclodextrin HPB and HP-Parenteral grade

KLEPTOSE® HPB & HP hydroxypropyl-betacyclodextrin parenteral grade materials that are used as encapsulating agents for Rx injectables. These are modified betacyclodextrins for parenteral use. Modified betacyclodextrins used in parenteral preparations provide active substance stabilization improvement against light and oxidation as well as enhancement of solubilization of active pharmaceutical ingredients.

Molecular encapsulation with modified beta-cyclodextrins has become an accepted and useful tool for pharmaceutical developers. There are currently several pharmaceutical products containing modified cyclodextrin complexes on the market. Roquette has pioneered the industrial development of cyclodextrins with its KLEPTOSE® range of betacyclodextrins.

hydroxypropyl-betacyclodextrin (HPBCD) is a white, amorphous powder. The HPBCD molecule is a torus shaped ring with a polar hydrophilic outside and an apolar hydrophobic cavity. 

® Registered trademark(s) of Roquette Frères
    Pyrogen Free
    DMF Available
    GMP Certificate

    Applications

    • Injectables
      • Rx Injectables

    Functional Properties

    • Excipient
      • Encapsulating Agent
      • Solubilizer
      • Stabilizer

    Documents & Samples

    Cosmetics
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    Unfortunately hydroxypropyl-betacyclodextrin HPB HP_PARENTERAL GRADE are not available in $country.

    Product Types

    KLEPTOSE® HP PARENTERAL GRADE - #346114

    Key attributes: Molecular encapsulation, Improve injectable API solubility and/or stability
    Unfortunately this product is not available for sampling

    High molecular substitution (MS) = 0.81 - 0.99

    KLEPTOSE® HPB PARENTERAL GRADE - #346111

    Key attributes: Molecular encapsulation, Improve injectable API solubility and/or stability
    Unfortunately this product is not available for sampling

    Medium molecular substitution (MS) = 0.58 - 0.68

    KLEPTOSE® HPB-LB PARENTERAL GRADE - #346115

    Key attributes: Molecular encapsulation, Improve injectable API solubility and/or stability
    Unfortunately this product is not available for sampling

    Medium molecular substitution (MS) = 0.50 - 0.71

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    Regulation & Compliance

    Registrations may vary depending on local regulations

    Compliance

    • European Pharmacopoeia
    • United States Pharmacopeia

    Regulatory

    • A Drug Master File (DMF) is available. Please contact us to discuss this information

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