Compound
Sulphur dioxide
The antimicrobial and antioxidant on which most modern cidermaking depends, and whose effectiveness collapses as pH rises — which makes every sulphiting decision a pH decision first.
Also called SO2, Sulphite, Metabisulphite, Campden.
- Class
- Additives and processing aids
- Formula
- SO2
- How often it matters
- Present in every cider
What it does in cider
- Exists in three forms in equilibrium, and only the undissociated molecular form crosses microbial membranes and kills anything.
- Loses potency sharply as pH rises, because the equilibrium moves overwhelmingly towards the inactive bisulphite ion above pH 3.
- Binds irreversibly to acetaldehyde and reversibly to other carbonyls, so a large part of any addition is consumed doing no antimicrobial work at all.
- Inhibits polyphenol oxidase and destroys hydrogen peroxide, protecting colour and fresh aroma independently of its antimicrobial role.
- Selects between organisms rather than sterilising: it suppresses wild yeasts and most bacteria while Saccharomyces tolerates it, which is what makes a controlled inoculated ferment possible.
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.
- struck match
- burnt rubber at high free levels
- suppressed aroma
- bleached colour
Free sulphur dioxide becomes perceptible as a struck-match pungency at levels that vary with pH, because it is the molecular fraction that is smelled — the same free figure is far more obvious in a low-pH cider than a high-pH one.
Descriptors it is responsible for
Sensory records that name Sulphur dioxide as a cause. Each states the perception and the mechanism behind it.
- Struck match — The sharp, mineral, matchhead note of free sulphur dioxide above its perception threshold.
- Flinty — A sub-threshold reductive note read as struck flint rather than as sulphur, the mildest state of reduction.
- Geranium — The crushed-geranium-leaf note produced when lactic bacteria metabolise added sorbate — a fault with one cause and no remedy.
- Passion fruit — A penetrating tropical-sulphur note from volatile thiols released by yeast β-lyase activity.
- Wet stone — A cool, damp, faintly mineral impression, in cider a product of low-level sulphur compounds and high acidity rather than of minerals.
- Blackcurrant — A dark, slightly green berry note from sulphur-containing thiols, or from direct fruit addition.
The structure it moves
| Dimension | What it is |
|---|---|
| Freshness | Whether the drink smells and tastes of live fruit or of time and air. |
| Oxidative character | Nutty, bruised-apple, sherry-like or cardboard notes from exposure to air. |
| Fruit character | How 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.
2 separate analyses of sulphur dioxide. They are shown as they were measured, in their own contexts, and are not averaged — the same fruit grown somewhere else can genuinely give a different number.
Sulphur dioxide0.5–0.8 mg/L
context not recorded · Molecular (undissociated) SO2, calculated from free SO2 and pH · Andrew Lea
This is the target for the *molecular* fraction, not for free or total SO2, and confusing the three is the commonest error in sulphite practice. The free SO2 needed to reach it depends entirely on pH: a cider at pH 3.2 needs roughly a quarter of what a cider at pH 3.8 needs for identical protection.
Sulphur dioxide10.0 mg/L
context not recorded · European Union
A labelling trigger, not a technical or safety threshold. Above this concentration, expressed as total SO2, the presence of sulphites must be declared on the label as an allergen. It says nothing about whether the cider is adequately protected, and a cider below it is generally not protected at all.
Added or residual SO2, whose antimicrobial effect depends sharply on pH. Measured in milligrams per litre.
What forms it
Processes that put this compound into the drink, or increase how much of it is there.
Sulphiting
Adding sulphur dioxide to juice to suppress spoilage organisms and oxidative browning, at a level that only means anything once the juice pH is known.
Sulphite stabilisation
Managing free sulphur dioxide through maturation and at packaging so that a useful antimicrobial and antioxidant fraction survives into the bottle.
Juice storage
Holding unfermented juice sound between pressing and fermentation, by chilling, sulphiting, gas blanketing, freezing or aseptic filling.
What removes or limits it
Processes that reduce it, hold it below a threshold, or stop it forming in the first place.
Oxidative maturation
Ageing a cider with a deliberate, measured oxygen supply so that tannins polymerise and soften and an aldehydic character develops on purpose, which is not the same thing as the oxidation fault.
Juice oxidation
The enzymic browning that begins the moment apple juice meets air, which some traditions deliberately allow and others suppress.
Tank maturation
Resting cider in stainless steel or a lined vessel, where the point of the container is that it contributes nothing and admits almost no oxygen.
Racking
Moving cider off the sediment it has thrown, which both cleans the liquid and — by taking yeast and nitrogen away with the deposit — slows what is left of the ferment.
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.
Excess sulphur dioxide
A struck-match or burnt-match aroma and a prickle at the back of the nose from too much free sulphur dioxide, with a real health consideration for sulphite-sensitive people.
Oxidation
The cumulative effect of oxygen on finished cider: fruit aroma flattens, colour deepens towards amber, and a bruised-apple or sherry-like character replaces the fresh one.
Unwanted refermentation
Fermentation restarting in a sealed container, generating carbon dioxide that was not planned for and pressure that a bottle may not withstand.
Colour loss
A cider left noticeably paler than it should be, usually because fining, filtration or sulphite has removed the phenolic material that gave it colour.
Geranium taint
A sharp, unmistakable crushed-geranium-leaf smell produced when lactic acid bacteria metabolise sorbic acid added as a preservative.
Stuck fermentation
A fermentation that has stopped before the sugar is gone and will not restart, leaving a sweet, low-alcohol cider that is vulnerable to everything.
Acetaldehyde excess
A bruised-apple, green-nut or sherry aroma from acetaldehyde, produced by oxidation, by film yeast, or left behind by a ferment that was interrupted.
Enzymatic browning
The rapid darkening of milled fruit and fresh juice as polyphenol oxidase converts phenolics to quinones, taking colour and some tannin structure with it.
Low acidity
A cider without enough acid to give it definition, tasting soft, heavy and dull — and sitting at a pH that leaves it exposed to spoilage organisms.
Microbial haze
Cloudiness caused by a growing population of spoilage organisms, and therefore a symptom of something worse rather than a clarity problem in itself.
Plastic and packaging taint
Plastic, rubber, adhesive or chemical notes picked up from unsuitable containers, liners, hoses, gaskets or cleaning residues.
Reduction
A closed, stale, slightly sulphurous character in cider held under strongly oxygen-free conditions, sometimes clearing with air and sometimes not.
Under-carbonation
A cider intended to sparkle that has little or no dissolved gas, usually because the bottle conditioning never started or the closure did not hold.
Atypical ageing
A cider that loses its fruit unusually early and develops a flat, faintly acrid or naphthalene-like character — a syndrome described in white wine and less firmly established in cider.
Pinking
An unexpected pink or salmon tint developing in a pale cider or perry, associated with oxidation of colourless phenolic precursors.
Organisms that produce it
Which organism is responsible usually decides whether the compound is a feature or a symptom.
Saccharomyces cerevisiae
The yeast that finishes essentially every cider, whether it arrives in a sachet or from the fruit, the press and the vessel.
Dekkera bruxellensis
The yeast behind 4-ethylphenol, and the organism that a cider tradition may regard as its signature or its ruin depending on where and how it is made.
Zygosaccharomyces bailii
A preservative-resistant spoilage yeast that refements sweetened cider and juice, and one of very few organisms able to grow through sorbate and benzoate at cider strength.
Acetobacter aceti
An acetic acid bacterium that oxidises ethanol to acetic acid wherever cider meets air, and the organism behind most volatile acidity in cider.
Oenococcus oeni
The acid-tolerant lactic acid bacterium that carries out most deliberate malolactic fermentation, converting malic acid to lactic acid after the yeast has finished.
Hanseniaspora uvarum
The apiculate yeast most often reported from grapes and widely present on apples too, whose anamorph name *Kloeckera apiculata* still appears throughout older cider literature.
Described in full
- What is plotted
- The vertical axis is molecular sulphur dioxide as a percentage of free sulphur dioxide. The horizontal axis is juice pH, from 3.0 to 4.0. The curve is calculated, not sketched: the molecular fraction is one divided by one plus ten to the power of pH minus 1.81.
- Why only the molecular form counts
- Free sulphur dioxide is a mixture of molecular SO₂ and bisulphite. Only the molecular form is antimicrobial. Measuring free sulphite therefore tells you how much you added, not how much is working.
- The shape of the curve
- It falls steeply and then flattens. At pH 3.0 about six percent of the free sulphite is molecular; by pH 4.0 it is about six tenths of one percent. The active fraction falls roughly tenfold across one pH unit.
- What that means in practice
- To hold the commonly used protective level of 0.8 mg/L molecular SO₂ needs about 13 mg/L free sulphite at pH 3.0, about 50 mg/L at pH 3.6, and about 125 mg/L at pH 4.0.
- Why bittersweet juice is the hard case
- Low-acid bittersweet fruit ferments at a high pH, exactly where sulphite is least effective, and where the sulphite dose required approaches or exceeds legal and sensory limits. This is a large part of why sharp fruit is blended in.
- The 1.81 in the expression
- It is the first acid dissociation constant of sulphurous acid, expressed as pKa. The equation is the Henderson–Hasselbalch relationship applied to that equilibrium, which is why the curve is a property of the chemistry rather than an empirical fit.
- A caution
- Bound sulphite is not shown at all. A substantial fraction of any addition binds irreversibly to acetaldehyde and other carbonyls and never contributes to the free figure, so the dose added always exceeds the free level measured afterwards.
About Sulphur dioxide
Dissolve sulphur dioxide in a cider and it immediately distributes itself between three species: molecular SO2, the bisulphite ion, and the sulphite ion. Only the first of these does the antimicrobial work. It is uncharged, so it crosses cell membranes freely, and inside the cell — where the pH is higher — it dissociates, acidifies the cytoplasm and reacts with essential thiols and cofactors. The charged ions cannot cross a membrane and are, for this purpose, inert.
The proportion in the active form is fixed by pH, through the first dissociation constant, which sits at about 1.81. The arithmetic is unforgiving. At pH 3.0 roughly six per cent of the free sulphur dioxide is molecular; at pH 3.5 about two per cent; at pH 3.8 about one per cent; at pH 4.0 well under one per cent. Since the target for meaningful protection is a molecular concentration of something like 0.5 to 0.8 mg/L, the free sulphur dioxide required to reach it rises from around 15 to 20 mg/L in a sharp cider to something over 100 mg/L in a cider at pH 4.0 — a level that would be organoleptically obvious and, in many jurisdictions, close to or above what the law permits. This is the whole reason a high-pH cider is hard to protect, and the reason a sulphiting decision cannot be made from a rate table without knowing the pH.
The second complication is binding. Sulphur dioxide reacts with carbonyl compounds, and the reaction with acetaldehyde is strong enough to be effectively permanent on cellar timescales. Bound sulphite is not molecular, not free, and not doing anything, but it is counted in total SO2 and therefore against any legal maximum. Juice from rotten or oxidised fruit is full of binders — acetaldehyde, pyruvate, ketonic compounds from mould metabolism, oxidation products of galacturonic acid — so it swallows large additions and shows almost no free SO2 the next morning. The useful conclusion is that sorting fruit is a sulphite-saving measure, and that a maker who responds to disappearing sulphite by adding more is paying twice for nothing.
What sulphur dioxide is actually used for varies with the stage. In juice it inhibits polyphenol oxidase and suppresses the wild yeast and bacterial population, which is what makes a predictable inoculated fermentation possible — and correspondingly, a maker who wants a wild ferment is choosing to forgo it, or to use a small addition that selects rather than sterilises. In finished cider it protects against refermentation, against acetic bacteria and against oxidation, both by scavenging oxidation products and by destroying the hydrogen peroxide generated when phenolics oxidise. It is also the necessary partner to sorbate, which does nothing to lactic bacteria and produces the geranium fault if they are left unchecked.
Two limits sit around all of this. The legal one is that maximum permitted concentrations are set by food additive law in each jurisdiction and are stated as total rather than free SO2, and that above 10 mg/L the label must declare sulphites. The human one is that a minority of people, most notably some with asthma, react to sulphites, which is precisely why the declaration exists. Neither of these is a reason to treat sulphur dioxide as sinister; both are reasons to use the smallest amount that does the job, and to make that judgement from the pH rather than from habit.
Related compounds
Compounds it is formed from, converted into, confused with, or routinely met alongside.
Aldehydes
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.
Gases
Dissolved oxygen
Essential to a healthy yeast population at the start of fermentation and the principal enemy of a cider from the moment fermentation ends.
Enzymes
Polyphenol oxidase
The copper enzyme that turns cut apple brown within seconds, and the reason a cidermaker has to decide, at the press, whether to let the juice oxidise or to stop it.
Acids
Galacturonic acid
The sugar acid that pectin chains are built from, released as they break down, and a significant part of why juice from rotten fruit binds so much of the sulphite added to it.
Additives and processing aids
Ascorbic acid
An oxygen scavenger that protects colour and aroma while it lasts and can promote browning once it is exhausted, which is why it is never used without sulphur dioxide.
Additives and processing aids
Potassium sorbate
The soluble salt in which sorbic acid is actually added, used to hold sweetness in a bottled cider, and dangerous to use without sulphite because of what lactic bacteria do to it.
Phenolics
Anthocyanins
The red pigments of apple skin and red-fleshed cultivars, which are colour rather than flavour and which fade quickly in a cider unless the pH is low.
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.
- Which yeast ferments cider — Saccharomyces cerevisiae finishes almost every cider fermentation, whether it was pitched or arrived from the press house. In a spontaneous ferment it is not the first organism present, only the one that survives the alcohol it makes.
- What is oxidation in cider
- Why did my sweetened cider start fermenting again — Live yeast met the sugar that was added back. Sweetening is only stable if the yeast has been removed by sterile filtration, killed by pasteurisation, or held in check by sorbate together with sufficient sulphite.
- What is brettanomyces — *Brettanomyces*, correctly *Dekkera* in its spore-forming form, is a slow yeast that ferments sugars other strains leave behind and produces volatile phenols smelling of farmyard, leather or sticking plaster. In cider it is common and not always unwanted.
- What turns cider into vinegar — Acetic acid bacteria oxidising ethanol, in two steps that both consume oxygen. This is why acetification is an air problem: a full sealed vessel does not acetify however many bacteria it contains.
- Which bacterium carries out malolactic fermentation in cider — Oenococcus oeni, in cider as in wine. Genome studies find that the cider strains are genetically distinguishable from the wine ones and that the strain most basal to the whole species was isolated from cider.
Where to go next
- All compounds — Grouped by what the fruit brings and what the ferment makes of it.
- Sensory — Every descriptor, with the compound or process that causes it.
- Microbiology — The organisms whose metabolism most of this chemistry belongs to.
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.
The Science of Cidermaking and associated technical writing
Andrew Lea · reference work · passage verified 2026-08-24
Written by a food chemist who worked at Long Ashton on apple phenolics. Unusual among specialist cider writing in that it is primary-research-adjacent: the author is describing work he did, and cites the literature. This is why it is registered at tier 1 for chemistry while a general cider book is not.
Cider and perry production technical training material
Peter Mitchell / Cider and Perry Academy · reference work · registered as competent for this subject
Searched again on 2026-08-25 and it remains the one printed source here that a bibliographic check cannot fix, because it is not a published work with an edition. It is course material issued to participants of a training programme, so there is no catalogue record to verify, no ISBN, and no lawful public copy. Its state stays `registered` for that reason rather than through inattention.
Regulation (EU) No 1169/2011 on the provision of food information to consumers
European Union · legislation · passage verified 2026-08-24
The instrument behind the "contains sulphites" declaration and the alcoholic-strength labelling rule. Read on 2026-08-24 in the assimilated text maintained on legislation.gov.uk, which is the version in force for Great Britain and keeps the EU numbering. Two provisions matter to cider and both are widely misquoted: the sulphite threshold is 10 mg/L rather than a percentage, and a labelled cider strength carries a tolerance of a full percentage point either way — twice what still grape wine is allowed.
Food labelling and packaging guidance
Food Standards Agency / Department for Business and Trade · regulator · retrieved 2026-08-24
European Food Safety Authority scientific opinions
EFSA · regulator · retrieved 2026-08-24
Registered for the food-safety questions cider genuinely raises: patulin in juice from rotten fruit, sulphite sensitivity, and the toxicology behind additive limits.
Codex Alimentarius food standards
FAO / WHO · standards body · retrieved 2026-08-24