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Pharm-Rx Mannitol

Pharm-Rx Mannitol is classified under active pharmaceutical ingredients (APIs) in the pharmaceuticals and nutraceuticals technologies, consists of D-mannitol, and is utilized in various healthcare and pharma markets, Pharm-Rx Mannitol is particularly in drug delivery and care solutions.

Chemical Name: D-mannitol

CAS Number: 69-65-8

Chemical Inventories: AICS (Australia), DSL (Canada), ECL (Korea), EINECS (EU), ENCS (Japan), IECSC (China), NZIoC (New Zealand), PICCS (Phillipines), TCSI (Taiwan), TSCA (USA)

Certifications & Compliance: California Proposition 65, FDA 29 CFR 1910.1200

Synonyms: 1,2,3,4,5,6-Hexanehexol, Cordycepic Acid, D-(-)-Mannitol, Manicol, Manitol

    Knowde Enhanced TDS

    Identification & Functionality

    Chemical Name

    D-mannitol

    Molecular formula
    C₆H₁₄O₆
    Technologies

    Pharmaceuticals & Nutraceuticals

    Product Families

    Pharmaceuticals & Nutraceuticals — Pharmaceutical Actives & Precursors

    Active Pharmaceutical Ingredients (APIs)

    Definition

    Mannitol contains not less than 97.0% and not more than 102.0% of mannitol (C₆H₁₄O₆), calculated on the dried basis.

    Chemical Structure

    - 1

    Applications & Uses

    Markets

    Healthcare & Pharma

    Applications

    Healthcare & Pharma — Drug Delivery & Care Solutions

    Other Drug & Care Solutions

    Properties

    Physical Form

    Powder

    Solubility

    Alkali Soluble,

    Aniline Soluble,

    Water Soluble

    Typical Properties
    ValueUnitsTest Method / Conditions
    Molecular Weight182.17——

    Regulatory & Compliance

    Certifications & Compliance

    California Proposition 65,

    FDA 29 CFR 1910.1200

    Chemical Inventories

    AICS (Australia),

    DSL (Canada),

    ECL (Korea),

    EINECS (EU),

    ENCS (Japan),

    IECSC (China),

    NZIoC (New Zealand),

    PICCS (Phillipines),

    TCSI (Taiwan),

    TSCA (USA)

    USP Reference Standards
    • USP Mannitol RS

    Packaging & Availability

    Labelling Information

    The label states, where applicable, the maximum concentration of bacterial endotoxins. The label states, where applicable, that the substance is suitable for use in the manufacture of parenteral dosage forms.

    Storage & Handling

    Storage Information

    Preserve in well-closed containers.