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Compound

p-Coumaroylquinic acid

The second most abundant hydroxycinnamic ester in apple, and the reservoir from which the p-coumaric acid behind 4-ethylphenol is slowly released.

Class
Phenolics
Formula
Not a single molecule — see below
How often it matters
Specialist — met in particular circumstances

What it does in cider

What forms it

Processes that put this compound into the drink, or increase how much of it is there.

What removes or limits it

Processes that reduce it, hold it below a threshold, or stop it forming in the first place.

Faults it is implicated in

Being implicated is not the same as being a fault. Several of the compounds on this site are ordinary constituents of a sound cider and define a named fault only above a concentration.

Organisms that produce it

Which organism is responsible usually decides whether the compound is a feature or a symptom.

About p-Coumaroylquinic acid

Where chlorogenic acid is caffeic acid bound to quinic acid, p-coumaroylquinic acid is p-coumaric acid bound to the same partner, and in most apple juices it is the second most abundant member of the hydroxycinnamic ester pool. Its single ring hydroxyl makes it a poorer substrate for polyphenol oxidase than chlorogenic acid, so it survives the browning of a juice better and carries further into the finished cider.

Its interest is as a reservoir. 4-Ethylphenol, the compound most responsible for the sticking-plaster and horse-blanket end of cider aroma, is made from free p-coumaric acid, and free p-coumaric acid in a cider comes mostly from the slow hydrolysis of this ester. A cider therefore has a stock of potential phenolic character built in from the fruit, which will be realised or not depending on whether the organisms capable of using it are present.

This explains a pattern that otherwise looks arbitrary: two barrels of the same cider, both carrying Dekkera, can differ substantially in phenolic intensity depending on how much bound precursor the fruit supplied and how long the cider has had to release it.

Related compounds

Compounds it is formed from, converted into, confused with, or routinely met alongside.

What people ask next

Questions readers ask about the things this page mentions. Each one goes to the section that answers it rather than to a page written to receive the question.

Where to go next

Sources

What this page rests on. Where a source is marked as registered rather than read, CiderHQ is recording that the body is authoritative on the subject without claiming to have worked through the document itself. See our evidence policy for what each state means.