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Oxidation of Hop Acids

Hop α- and β-acids, and particularly iso-α-acids, undergo oxidation reactions during ageing, resulting in the loss of bitterness.

It has been shown that volatile carbonyls can be produced from a solution of bitter substances, higher alcohols and melanoidins. The trans isomers are more prone to degradation than the cis isomers. Reduced hop products do not participate in these reactions.

Other aromas, described as rancid, sweaty socks and cheesy can be formed from the oxidation of α- and β-acids. These aromas are imparted by free acids originating from the oxidation of the acyl side-chain of the acidic resin fractions. The main reactants are:

  • Isobutyric

  • Isovaleric

  • 2-Methyl butyric acid

In addition, ethyl esters consequently formed from these acids, contribute to a stale hop character.

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