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Compound

Acetaldehyde

The compound sitting one step short of ethanol, which smells of bruised apple and sherry, binds most of the sulphite added to a cider, and is the chemical signature of oxidation.

Also called Ethanal.

Class
Aldehydes
Formula
CH3CHO
How often it matters
Present in every cider

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

Free acetaldehyde is perceptible well below the total figure, because bound acetaldehyde is not smelled at all. Sensory thresholds quoted for wine sit in the region of a hundred milligrams per litre of total acetaldehyde, but in a cider carrying little free sulphur dioxide the same total is far more obvious.

Descriptors it is responsible for

Sensory records that name Acetaldehyde 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
Oxidative characterNutty, bruised-apple, sherry-like or cardboard notes from exposure to air.
FreshnessWhether the drink smells and tastes of live fruit or of time and air.
Fruit characterHow strongly the drink smells of apple or pear, and of fruit generally.

Measured figures

Shown as they were measured, with the context each was taken in. They are not averaged: a concentration recorded in one country's fruit in one decade is not a constant.

Acetaldehyde2.0–3.0 mg/L

Villaviciosa, Asturias, Spain, 2001–2002 · 4 samples · Gas chromatography with flame ionisation detection · Suárez Valles, Pando Bedriñana, Fernández Tascón, Querol Simón and Rodríguez Madrera, Food Microbiology 24(1):25–31

Sound, fully fermented cider that had not been sulphited. Acetaldehyde binds sulphur dioxide, so a sulphited cider of the same age can carry considerably more of it while smelling of less; and an oxidising cider climbs well above this band. The figure describes healthy cider, not a limit.

The intermediate between sugar and ethanol, which is also what oxidation turns ethanol back into — so the same number can mean a young ferment or an old fault. Measured in milligrams per litre.

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 Acetaldehyde

Every molecule of ethanol in a cider passed through acetaldehyde on the way. Yeast decarboxylates pyruvate to acetaldehyde and then reduces acetaldehyde to ethanol, and in a healthy ferment the intermediate rises during the vigorous phase and is largely reclaimed as the ferment finishes. A ferment that is stressed, sulphited heavily at the start, or stopped abruptly leaves more of it behind, which is one reason an arrested fermentation can taste flatter than expected.

In a finished cider the compound arrives by a different route: oxidation. Acetic acid bacteria oxidise ethanol to acetaldehyde as their first step, film yeasts do the same at an exposed surface, and there is a purely chemical route as well, in which phenolic compounds oxidised by air generate hydrogen peroxide that oxidises ethanol directly. That last route matters because it needs no organism at all — a sound, sterile cider left in contact with air will still develop acetaldehyde, and the more phenolic it is the faster it does so.

The sulphite relationship is the practically important one. Acetaldehyde reacts with bisulphite to form a hydroxysulphonate, and the binding is strong enough to be effectively irreversible on cellar timescales. Bound sulphite has no antimicrobial activity whatever, so a cider carrying acetaldehyde consumes its sulphite additions without gaining protection. This is why an oxidised or bacterially spoiled batch seems to swallow sulphite: the added SO2 is being locked to the aldehyde rather than doing any work. It is also why measured total SO2 can be high while free SO2 — the only fraction that protects anything — is negligible.

The same reaction runs in the other direction as a treatment, and it deserves stating carefully. Binding acetaldehyde removes its smell, so a modest sulphite addition can make a lightly oxidised cider taste noticeably fresher. Nothing has been repaired: the aldehyde is still there, the sulphite has been consumed, and the cider is now less protected than the analysis of total SO2 suggests. Meanwhile, in styles built on air — traditional Asturian sidra, some barrel-matured English and Norman ciders — the same compound is not a fault at all but a recognised part of the character, judged against expectations the style established long before anybody could measure 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.