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    Disproportionated Rosin

    Disproportionated Rosin in Tradeasia

    IUPAC Name

    -

    Cas Number

    8050-09-7

    HS Code

    38069090

    Formula

    C20H30O2

    Basic Info

    Appearance

    Light Yellow Transparent Solid

    Common Names

    DPR

    Packaging

    Galvanized Iron Drum, 220kg net each, 22MT

    Brief Overview:

    Disproportionated rosin (DPR) is a compound consisting of dehydrogenated resin acids (dehydro-abietic acid) and hydrogenated resin acids (dihydro-abietic acid). It is produced from gum rosin by heating or acid treatment. DPR is commonly used in the form of a soap as an emulsifier in various products such as styrene-butadiene rubber, chloroprene rubber or acrylonitrile-butadiene-styrene rubber.

    Manufacturing Process:

    Disproportionated rosin is obtained by heating rosin mixtures at temperatures of 180-350 C for a sufficient time to reduce the abietic acid content to below 15%. The disproportionation process displaces the hydrogen in the abietic acid of the rosin to convert them into isomeric acids, particularly dehydroabietic acid, which lack nonbenzenoid double bond conjugation and are therefore more stable to oxidation than abietic acid. 

    Brief Overview:

    Disproportionated rosin (DPR) is a compound consisting of dehydrogenated resin acids (dehydro-abietic acid) and hydrogenated resin acids (dihydro-abietic acid). It is produced from gum rosin by heating or acid treatment. DPR is commonly used in the form of a soap as an emulsifier in various products such as styrene-butadiene rubber, chloroprene rubber or acrylonitrile-butadiene-styrene rubber.

    Manufacturing Process:

    Disproportionated rosin is obtained by heating rosin mixtures at temperatures of 180-350 C for a sufficient time to reduce the abietic acid content to below 15%. The disproportionation process displaces the hydrogen in the abietic acid of the rosin to convert them into isomeric acids, particularly dehydroabietic acid, which lack nonbenzenoid double bond conjugation and are therefore more stable to oxidation than abietic acid. 

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