Science
Mechanism of Action
Functions as a prodrug that penetrates skin and undergoes enzymatic hydrolysis by esterases to release pure vitamin C. Once converted, it scavenges reactive oxygen species, inhibits tyrosinase to reduce melanin production, and serves as an essential cofactor for collagen synthesis enzymes. The glyceryl component provides additional humectant benefits for enhanced skin barrier function.
Research
Clinical Evidence
Medium confidence1%
Key findings
- 01 Clinical trials demonstrated maximum permeability enhancement at 1.0% concentration, with no additional benefits observed at higher percentages
Transparency
Dusting Analysis
Given the established 1% optimal efficacy threshold, concentrations below 0.5% may represent symbolic inclusion rather than therapeutic dosing.
The Formula
Formulation
Stability
Exceptional stability profile compared to L-ascorbic acid, maintaining integrity at 50°C without requiring ultra-low pH conditions below 3.5
Synergies
- Vitamin E
- Ferulic acid
- Hyaluronic acid
Conflicts
- Strong oxidizing agents
- Strong alkaline ingredients
- Cationic surfactants
Safety
Safety Profile
Covered under CIR safety assessment for ascorbic acid ethers and esters, with typical cosmetic usage ranging 1-7% depending on formulation
Your Skin
Skin Compatibility
Our Assessment
Verdict
A scientifically sound vitamin C derivative that delivers stability advantages over pure ascorbic acid with demonstrated clinical efficacy at 1% concentration.
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References
Sources