Recombinant Bovine Somatotropin vs Azodicarbonamide: which is worse?
Quick answer: Azodicarbonamide carries the heavier risk profile. Recombinant Bovine Somatotropin is — in the EU and — in the US; Azodicarbonamide is — in the EU and — in the US.
| Property | Recombinant Bovine Somatotropin | Azodicarbonamide |
|---|---|---|
| EU status | — | — |
| US status | — | — |
| Risk level | — | — |
| Banned in | European Union, Canada, Japan, Australia, New Zealand | European Union, United Kingdom, Australia, New Zealand, Singapore |
| Restricted in | — | Canada (not approved for food use) |
| Category | additive | additive |
| Where it hides | — | — |
What is Recombinant Bovine Somatotropin?
Recombinant bovine somatotropin (rBST) is the synthetic version of bovine growth hormone (BST), naturally produced by the pituitary gland in cattle. The recombinant version is produced using genetically engineered bacteria and is injected into dairy cows to increase milk production by 10-15%. Brand name: Posilac.
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
Recombinant Bovine Somatotropin: See recombinant-bovine-growth-hormone-rbgh for full detail. Key concerns: rBST elevates IGF-1 in milk; elevated blood IGF-1 is associated with breast, prostate, and colorectal cancer risk in epidemiological studies. Animal welfare: increased mastitis (up to 25-50% higher rates), lameness, and antibiotic use. The Codex Alimentarius Commission declined to endorse rBST safety MRLs in a historic 33-29 vote. Health Canada rejected rBST approval in 1999 after finding it caused significant animal health problems requiring increased antibiotic use.
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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