How we scored it
How it’s made
Where it comes from
Industrial allantoin is made by reacting urea (from natural-gas ammonia) with glyoxylic acid, a fully synthetic route. Comfrey-root-extracted allantoin exists but is not the dominant commercial cosmetic-grade source.
The most common industrial synthesis of Allantoin involves the reaction of urea with glyoxylic acid. This reaction is typically carried out in an aqueous medium under acidic conditions. Glyoxylic acid can be produced through various methods, including the oxidation of glyoxal or the ozonolysis of maleic acid. However, the urea feedstock is the dominant factor in determining the natural origin of the final product.
The reaction proceeds via a condensation mechanism. Urea, acting as a nucleophile, attacks the carbonyl carbon of glyoxylic acid. This is followed by cyclization and dehydration steps to form the allantoin molecule. The reaction conditions are generally mild, often involving heating the mixture to moderate temperatures (e.g., 50-100°C) for several hours.
Purification of the crude allantoin is crucial to obtain a cosmetic-grade product. This typically involves recrystallization from water or other suitable solvents. The process removes unreacted starting materials, byproducts, and inorganic salts. Filtration, washing, and drying are standard steps to isolate the pure allantoin crystals, which are then characterized for purity and quality before use in cosmetic formulations.
In plain English
Allantoin is a popular ingredient in skincare products, known for its soothing and skin-conditioning properties. It helps to calm irritated skin, promote cell regeneration, and leave the skin feeling smooth and soft. You'll often find it in moisturizers, lotions, and products designed for sensitive or dry skin.
While allantoin occurs naturally in some plants like comfrey and in the urine of most mammals, the allantoin used in cosmetics is almost exclusively produced through a chemical synthesis process. This process typically starts with urea, a common chemical compound. Urea is then reacted with another chemical, glyoxylic acid, under controlled conditions to create allantoin.
Because the primary starting materials for this synthesis are derived from fossil fuels (like natural gas used to produce ammonia for urea), allantoin is considered a synthetic ingredient with no natural origin according to the ISO 16128 standard. This means it has a Natural Origin Index (NOI) of 0.0.
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Structure
(2,5-dioxoimidazolidin-4-yl)urea
References
- 1ISO 16128-1:2016 and ISO 16128-2:2017 — Guidelines on technical definitions and criteria for natural and organic cosmetic ingredients and products. ISO, Geneva.
- 2Allantoin. PubChem CID 204. National Center for Biotechnology Information. pubchem.ncbi.nlm.nih.gov ↗
- 3ALLANTOIN. CosIng — European Commission cosmetic ingredient database. ec.europa.eu/cosing ↗
- 4ALLANTOIN. CosIng u2014 European Commission database for information on cosmetic substances and ingredients. https://ec.europa.eu/growth/tools-databases/cosing/search?search=ALLANTOIN