
A compound known for its soothing and skin conditioning properties, commonly used in skincare products.
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CAS Number
97-59-6
HS Code
2933.21.0000
Molecular Formula
C₄H₆N₄O₃
INCI Name
Allantoin
A compound known for its soothing and skin conditioning properties, commonly used in skincare products.
CAS Number
97-59-6
INCI Name
Allantoin
HS Code
2933.21.0000
Molecular Formula
C₄H₆N₄O₃
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| Property | Specification |
|---|---|
| Ph | 4.5 - 6 (5% in water, 20 °C) |
| Odor | Odorless |
| Appearance | Colorless to white solid |
| Refractive Index | n20/D 1.442(lit.) |
| Molecular Weight (G/Mol) | 158.12 |
| Ph (If Aqueous Solution) | 4.5 - 6 (5% in water, 20 °C) |
| Density Or Specific Gravity | 0.951 g/mL at 25 °C (lit.) |
| Property | Specification |
|---|---|
| Pka | 8.96(at 25℃) |
| Property | Specification |
|---|---|
| Flash Point | 230-234°C |
| Boiling Point | Decomposes before boiling |
| Melting Point | 239 °C |
| Thermal Stability | Stable at room temperature; decomposes at high temperatures |
| Decomposition Temperature | Decomposes above melting point |
Dissolve allantoin in the water phase and heat to ensure complete solubility. Avoid adding during the cool-down phase, as it has limited solubility in cold water and may recrystallize.
| Key Ingredients | Indicative Dosage (% w/w) |
|---|---|
| Water (Aqua) | 70% |
| Glycerin | 5% |
| Cetearyl Alcohol | 4% |
| Caprylic/Capric Triglyceride | 6% |
| Isopropyl Myristate | 3% |
| Stearic Acid | 2% |
| Triethanolamine (TEA) | 0.8% |
| Benzalkonium Chloride (50% sol.) | 0.2% |
| Allantoin | 0.5% |
| Panthenol (Pro-Vitamin B5) | 1% |
| Tocopheryl Acetate (Vitamin E) | 0.5% |
| Dimethicone | 2% |
| Fragrance | 0.5% |
| Phenoxyethanol & Ethylhexylglycerin | 1% |
| Citric Acid (10% solution) | 0.4% |
Add allantoin to the heated water phase to ensure proper dissolution, as it has low solubility in cold water. Mix well to avoid grittiness or sediment in the final shampoo.
| Key Ingredients | Indicative Dosage (% w/w) |
|---|---|
| Primary surfactants | 8-12% |
| Secondary surfactants | 2-5% |
| Butters | 20-40% |
| Allantoin | 0.1–1% |
| Water | 40-50% |
| Other UV Filters, Antioxidants, Humectants, Fragrance/flavor etc. |
When formulating facial cleansers, dissolve Allantoin (typically 0.1–0.5%) in the water phase by heating to ensure full solubility. Avoid overheating, as Allantoin can degrade at high temperatures. Stir gently to maintain clarity in clear formulations.
| Key Ingredients | Indicative Dosage (% w/w) |
|---|---|
| Deionized Water | 70% |
| EDTA-2Na | 0.10% |
| Sodium Cocoamphoacetate | 10% |
| Cocamidopropyl Betaine | 8% |
| Glycerine | 5% |
| Lauryl Glucoside | 4% |
| Panthenol | 1% |
| Allantoin | 0.3% |
When adding allantoin to sunscreen, dissolve it in the water phase at 0.05–0.5% concentration and heat gently to ensure full solubilization. Maintain final pH between 5.0–7.0 for stability and compatibility with UV filters. Stir thoroughly to ensure uniform dispersion.
| Key Ingredients | Indicative Dosage (% w/w) |
|---|---|
| Homosalate | 6-10% |
| Ethylhexyl Methoxycinnamate | 5-9% |
| Ethylhexyl Salicylate | 2-6% |
| 4-Methylbenzylidene Camphor | 2-5% |
| Titanium Dioxide | 2-6% |
| Polydimethylsiloxane | 3-8% |
| Propylene Glycol | 3-6% |
| Allantoin | 0.05% to 0.3% |
| Plant extracts (e.g., safflower extract) | 0.3-0.6% |
| Emulsifiers and thickeners |
| Products | Authorized dosage % |
|---|---|
| Skin Care | 0.5-2% |
| Hair shampoo | 0.1-1% |
| Other Personal Care | 0.2-2% |
Condensation of urea with glyoxylic acid, followed by cyclization and oxidation. Yield recovery for the urea-glyoxylic acid process typically ranges from 80–90%.
1. Condensation of urea with glyoxylic acid, followed by cyclization and oxidation. Yield recovery for the urea-glyoxylic acid process typically ranges from 80–90%. Ran Material: Urea, Glyoxylic acid, Catalyst/oxidizing agent Overall Formula: C₂H₄N₂O₂ (Urea) + C₂H₂O₃ (Glyoxylic acid) → C₄H₆N₄O₃ (Allantoin) + H₂O
Oxidation of uric acid, a naturally occurring purine derivative. The yield recovery is typically around 60–75%.
2. Oxidation of uric acid, a naturally occurring purine derivative. The yield recovery is typically around 60–75%. Raw Material: Uric acid, Oxidizing agent (e.g., potassium permanganate or nitric acid), Water Overall Formula: C₅H₄N₄O₃ (Uric acid) + [O] → C₄H₆N₄O₃ (Allantoin)
Condensation of urea with glyoxylic acid, followed by cyclization and oxidation. Yield recovery for the urea-glyoxylic acid process typically ranges from 80–90%.
1. Condensation of urea with glyoxylic acid, followed by cyclization and oxidation. Yield recovery for the urea-glyoxylic acid process typically ranges from 80–90%. Ran Material: Urea, Glyoxylic acid, Catalyst/oxidizing agent Overall Formula: C₂H₄N₂O₂ (Urea) + C₂H₂O₃ (Glyoxylic acid) → C₄H₆N₄O₃ (Allantoin) + H₂O
Oxidation of uric acid, a naturally occurring purine derivative. The yield recovery is typically around 60–75%.
2. Oxidation of uric acid, a naturally occurring purine derivative. The yield recovery is typically around 60–75%. Raw Material: Uric acid, Oxidizing agent (e.g., potassium permanganate or nitric acid), Water Overall Formula: C₅H₄N₄O₃ (Uric acid) + [O] → C₄H₆N₄O₃ (Allantoin)
| Region | Max Allowed Level | Notes | Certification Body |
|---|---|---|---|
| United States | 2% | The US FDA list Allantoin as a over-the-counter (OTC) skin protectant at 0.5% to 2%. | FDA |
| European Union | - | No explicit legal maximum, can be used at any safe concentration | SCCS (Scientific Committee on Consumer Safety) |
| India | - | No BIS-specific limit | - |
| Japan | - | No specific limit | MHLW – Ministry of Health, Labour and Welfare |
| Australia | - | No statutory maximum | - |
| China | - | No statutory maximum | NMPA - National Medical Products Administration |
| Korea, Republic of | - | No statutory maximum | MFDS - Ministry of Food and Drug Safety |
| ASEAN | - | No statutory maximum | - |
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