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L478421-100mgDescriptionRefer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
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M108601-5mlMethyl acetoacetate undergoes asymmetric hydrogenation to form (R)-(-)-methyl-3-hydroxybutyrate in the presence of enantioselective Ni/SiO2 catalysts. It undergoes Pechmann reactions with phenols in various ionic liquids.Methyl acetoacetate was used
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M106479-100mgMethyl heptadecanoate.
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M106479-1gMethyl heptadecanoate.
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M107373-100mlMethyl myristate.
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M107373-25mlMethyl myristate.
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M107373-500mlMethyl myristate.
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M117559-1mlMethyl stearate solution.
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