Get a Free 5ml Mini Now Free 5ml Mini With Every Order of The Mantle
Moumoujus

GLYCIDYL METHACRYLATE/VA/VINYL CHLORIDE COPOLYMER.

Insufficient Data / FILM FORMING

This terpolymer is synthesized from glycidyl methacrylate, vinyl acetate, and vinyl chloride monomers. Characterized by the reactive epoxy groups derived from glycidyl methacrylate, it functions primarily as a cross-linking agent and adhesion promoter in various industrial applications. Direct efficacy and safety data for its use in precision skincare are currently unavailable.

Summary

Binding Agent Adhesion Promoter Cross-linking Agent Film Former

Science

Mechanism of Action

The copolymer's mechanism of action is primarily driven by the epoxy functionality contributed by its glycidyl methacrylate component. These epoxy groups enable high reactivity, facilitating cross-linking and enhancing adhesion within polymer systems. While this bifunctional nature is exploited for chemical modification and property enhancement in materials like waterborne polyurethanes or PVC, its specific biological mechanism when applied directly to human skin in cosmetic formulations is not documented in the available scientific literature.

Research

Clinical Evidence

Insufficient-data confidence
Effective range N/A
Optimal

N/A

Transparency

Dusting Analysis

Not commonly dusted

The Formula

Formulation

Solubility
Unknown
Optimal pH N/A
0 7 14

Stability

The glycidyl methacrylate component introduces reactive epoxide groups into the copolymer structure, rendering it susceptible to various chemical reactions, including cross-linking. The reactivity of these epoxy groups can be influenced by their spatial orientation, the presence of other polar groups, steric bulk, solvent type, and temperature. Comprehensive stability data specifically for this terpolymer in cosmetic formulations are not currently available.

Safety

Safety Profile

CIR Status
Not reviewed
Sensitization risk Unknown

GLYCIDYL METHACRYLATE/VA/VINYL CHLORIDE COPOLYMER has not been specifically reviewed by either the Cosmetic Ingredient Review (CIR) or the Scientific Committee on Consumer Safety (SCCS) for its safety in cosmetic applications. While FDA regulations permit similar polymers of glycidyl methacrylate for indirect food contact as components in adhesives and coatings (e.g., 21 CFR 175.105, 175.300, 176.180), this does not equate to direct cosmetic approval. Importantly, Glycidyl Methacrylate (GMA), the monomer precursor, is classified as a highly reactive substance, highly toxic by inhalation, and a severe irritant and corrosive agent to skin, eyes, and the respiratory tract. It has also been identified as a dermal sensitizer in animal models and is listed by the State of California as a chemical known to cause cancer. While the safety profile of a polymer can differ significantly from its monomer, direct safety data for this specific copolymer in cosmetic contexts is critically absent, raising significant cautionary flags given the monomer's profile.

Your Skin

Skin Compatibility

No Normal
No Dry
No Oily
No Sensitive
Irritancy Unknown
Comedogenicity Unknown

Our Assessment

Verdict

Insufficient Data

Due to a complete absence of specific safety and efficacy data for this copolymer in cosmetic applications, coupled with serious toxicity and carcinogenicity concerns associated with its monomer, its suitability for skincare cannot be determined.

Related

Similar Ingredients

Finding similar ingredients…

References

Sources