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Compound

trans-2-Hexenal

The sharper, more penetrating green aldehyde of the same pathway as hexanal, made from linolenic rather than linoleic acid, and a marker of underripe fruit.

Also called (E)-2-hexenal, Leaf aldehyde.

Class
Aldehydes
Formula
C6H10O
How often it matters
Specialist — met in particular circumstances

What it does in cider

How it is perceived

What the compound registers as, and at roughly what concentration. Perception is not a property of the molecule alone: sugar, tannin and carbonation all change where a threshold falls.

On threshold

Perceived as harsher and more intrusive than hexanal at comparable concentration, and a recognised marker of green, underripe fruit character in fresh juice.

Descriptors it is responsible for

Sensory records that name trans-2-Hexenal as a cause. Each states the perception and the mechanism behind it.

The structure it moves

Structural dimensions this compound contributes to. Direction and amount depend on concentration and on what else is in the drink; the dimensions themselves are set out in full under Sensory.
DimensionWhat it is
Fruit characterHow strongly the drink smells of apple or pear, and of fruit generally.
FreshnessWhether the drink smells and tastes of live fruit or of time and air.

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.

About trans-2-Hexenal

The lipoxygenase pathway acts on two membrane fatty acids and produces two different green notes. Linoleic acid gives hexanal, which reads as cut grass and fresh apple. Linolenic acid gives trans-2-hexenal, which reads as leaf and stem and is distinctly harsher — the smell of a torn leaf rather than a mown lawn.

Underripe fruit carries proportionally more linolenic acid, so juice pressed from fruit picked early is greener in this specific, unattractive way, and the difference is one of the sensory arguments for leaving cider fruit on the tree or in store until it is properly ready.

Like hexanal it is largely reduced by yeast during fermentation and is not usually a feature of finished cider. It is a juice compound, most relevant to anyone tasting through a pressing to judge the fruit.

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.