INCI Name
Retinol
Functions
2 Roles
Sustainability
6/10
Category
actives
What It Does
Retinol is the pure alcohol form of Vitamin A and is considered the gold standard anti-aging active in cosmetic formulations. It is highly unstable and sensitive to light, air, and heat, requiring careful encapsulation or stabilization systems to maintain efficacy. Formulators choose retinol for its clinically proven ability to stimulate collagen production, accelerate cell turnover, and improve skin texture, though it requires concentrations typically between 0.01-1% and must be formulated in anhydrous or specially stabilized systems to prevent degradation.
Technical Properties
Ionic Charge
nonionic
Molecular charge type
Viscosity Effect
neutral
Impact on formula thickness
Ingredient Compatibility
Known Interactions
Benzoyl Peroxide oxidizes and deactivates Retinol on contact. These must never be in the same formulation.
Retinol and L-Ascorbic Acid both require low pH but Retinol is unstable in acidic conditions. Using both in the same formula reduces efficacy of both actives. Separate into AM (Vitamin C) and PM (Retinol) products.
Retinol combined with Glycolic Acid significantly increases irritation potential. The low pH required for Glycolic Acid (pH 3.0-4.0) destabilizes Retinol. Use in separate products.
Retinol is destabilized by the low pH required for Lactic Acid efficacy (pH 3.5-4.0). Combined use increases irritation without proportional benefit. Use in separate products.
Mandelic Acid requires low pH (3.0-4.0) that destabilizes Retinol. While less irritating than Glycolic Acid, the pH conflict remains. Use in separate products.
Retinol and Salicylic Acid together increase irritation risk. Salicylic Acid's optimal pH (2.5-4) destabilizes Retinol. Best used in separate routines.
Copper peptides and Retinol operate through competing pathways (copper promotes collagen synthesis while retinol increases cell turnover). Combined use may increase irritation and reduce peptide stability.
Avobenzone (Butyl Methoxydibenzoylmethane) can accelerate Retinol photodegradation. If combining in a day product, use encapsulated Retinol or a photostabilized Avobenzone.
Sustainability Profile
Sustainability Score
Biodegradability
readily biodegradable
Source
synthetic
Feedstock
Typically synthesized from beta-ionone or produced through chemical modification of retinyl esters
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Quick Reference
- Full INCI Name
- Retinol
- Common Name
- Vitamin A
- CAS Number
- 68-26-8
- Category
- actives
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