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    Butyl Acetate (99%) - China

    Butyl Acetate (99%) - China in Tradeasia

    IUPAC Name

    Butyl Acetate

    Cas Number

    123-86-4

    HS Code

    2915.33.00

    Formula

    C6H12O2

    Basic Info

    Appearance

    Transparent Liquid

    Common Names

    Butyl Ethanoate

    Packaging

    180 KG Metal Drum

    Brief Overview 

    Butyl acetate, also called butyl ethanoate, is an organic compound with medium volatility and a characteristic fruity ester odor. It is found in many types of fruit, where, along with other chemicals, it imparts characteristic flavors and has the sweet scent of banana or apple. Butyl acetate is a medium-boiling ester solvent. It is highly flammable and miscible with all common organic solvents, but has only slight miscibility in water. Butyl acetate is volatile in the atmosphere and undergoes photochemical oxidation reactions with hydroxyl radicals and chlorine atoms.

    Manufacturing Process 

    The esterification of butanol and acetic acid results in the formation of butyl acetate, with sulfuric acid serving as the catalyst. The removal of water through azeotropic separation drives the reaction to completion. Subsequently, the acid catalyst is neutralized, and the ester undergoes purification via distillation.

    Brief Overview 

    Butyl acetate, also called butyl ethanoate, is an organic compound with medium volatility and a characteristic fruity ester odor. It is found in many types of fruit, where, along with other chemicals, it imparts characteristic flavors and has the sweet scent of banana or apple. Butyl acetate is a medium-boiling ester solvent. It is highly flammable and miscible with all common organic solvents, but has only slight miscibility in water. Butyl acetate is volatile in the atmosphere and undergoes photochemical oxidation reactions with hydroxyl radicals and chlorine atoms.

    Manufacturing Process 

    The esterification of butanol and acetic acid results in the formation of butyl acetate, with sulfuric acid serving as the catalyst. The removal of water through azeotropic separation drives the reaction to completion. Subsequently, the acid catalyst is neutralized, and the ester undergoes purification via distillation.

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