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Propylene Glycol vs Azodicarbonamide: which is worse?

Quick answer: Azodicarbonamide carries the heavier risk profile. Propylene Glycol is in the EU and in the US; Azodicarbonamide is in the EU and in the US.

PropertyPropylene GlycolAzodicarbonamide
EU status
US status
Risk level
Banned inEuropean Union, United Kingdom, Australia, New Zealand, Singapore
Restricted inEuropean Union (not permitted as a direct food additive in most food applications; only permitted as a carrier solvent for specific additives at low levels)Canada (not approved for food use)
Categoryadditiveadditive
Where it hides

What is Propylene Glycol?

Propylene glycol is a synthetic organic compound used as a humectant, solvent, and emulsifier in food, pharmaceuticals, cosmetics, and industrial applications. It is produced from propylene oxide (derived from petroleum). Its chemical formula is C3H8O2.

What is Azodicarbonamide?

Azodicarbonamide (ADA) is a synthetic chemical used in the food industry as a flour bleaching agent and dough conditioner, and industrially as a blowing agent in foam rubber and plastic production. Its chemical formula is C2H4N4O2. When it reacts with water or heat, it breaks down into biurea (primary product) and semicarbazide (SEM).

Documented risks

Propylene Glycol: Propylene glycol is generally considered safe by the FDA and is metabolized by the liver to lactic acid and pyruvate (normal metabolites). However, at high doses — particularly from intravenous pharmaceutical formulations — propylene glycol can accumulate and cause lactic acidosis, kidney toxicity, and CNS effects. These effects are seen in critically ill patients receiving high-dose PG-containing intravenous medications, not from food consumption. In children and people with impaired liver or kidney function, PG accumulation may occur at lower doses than in healthy adults. Animal studies have found reproductive and developmental effects at high doses. EFSA's 2018 re-evaluation found no concerns at typical food use levels but noted the EU limits PG use as a direct food additive, using it only as a carrier solvent for permitted additives.

Azodicarbonamide: ADA's primary food safety concern is its breakdown to semicarbazide (SEM) during baking. In a 2002 study, SEM was found to increase the incidence of vascular tumors in female mice at high doses. This single animal finding was sufficient under the EU's precautionary principle to ban ADA in food use in 2005. The FDA conducted a comprehensive SEM exposure assessment in 2016, concluding that US population exposure to SEM from ADA-treated bread is many orders of magnitude below doses showing tumor effects in rodents and does not warrant regulatory change. This reflects the FDA's risk-based approach. Urethane (ethyl carbamate) is another potentially harmful breakdown product of ADA. Urethane is classified as an IARC Group 2A probable human carcinogen. Small amounts of urethane can form from SEM in fermented or alcohol-containing environments. The 2014 'yoga mat chemical' controversy highlighted ADA's dual use: it is the same chemical used as a blowing agent in foam rubber and plastic manufacturing — including yoga mats. Consumer advocacy blogger Vani Hari's 'Food Babe' campaign led over 50,000 people to petition Subway, which voluntarily removed ADA from its bread in 2014. The dual industrial-food use raised public concern even though ADA's behavior in each context is chemically different. From occupational health: workers exposed to ADA powder in bakery or plastic manufacturing settings can develop occupational asthma. WHO recognizes ADA as a respiratory sensitizer in occupational settings, though dietary exposure through bread is fundamentally different from inhalation exposure.

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