Science
Mechanism of Action
This polymer utilizes cationic (positively charged) aminopropyl groups to selectively bond with the skin's naturally negative surface, particularly in damaged or dry areas. Its dual-length alkyl chains (C6-12 and C14-18) create a breathable, water-resistant lipid shield that enhances moisture retention while the acetylation process ensures a refined, odor-free sensory profile during application.
Research
Clinical Evidence
Medium confidence5%
Key findings
- 01 Demonstrated superior durability and comfort in color cosmetic matrices, preventing cracking on keratinous surfaces like the skin and lips.
Transparency
Dusting Analysis
In high-performance foundations or barrier creams, this ingredient should be present at 1% or higher to provide its signature film-forming and substantive benefits; concentrations below 0.1% are likely for marketing claims rather than functional efficacy.
The Formula
Formulation
Stability
Excellent stability in anhydrous formulas and both W/O and O/W emulsions. Requires careful pH management to prevent premature protonation of amino groups which can destabilize specific emulsion types.
Synergies
- Inorganic pigments
- Non-polar emollients
- Hydrophobically treated powders
Conflicts
- Anionic surfactants
- Strong oxidizing agents
Safety
Safety Profile
While this specific INCI is a newer modification, its parent classes (Amodimethicones and Alkyl Dimethicones) have an established safety profile in cosmetic use.
Your Skin
Skin Compatibility
Our Assessment
Verdict
A high-precision polymer essential for creating breathable, long-wearing barriers and improving the tactile finish of complex skincare and hybrid cosmetic formulas.
Related
Similar Ingredients
Finding similar ingredients…
References
Sources