Science
Mechanism of Action
This compound functions by inhibiting microbial proliferation, thereby acting as a preservative. Research indicates that the monoethyleneamine (MEA) moiety facilitates greater skin absorption compared to its parent compound, o-phenylphenol, which is posited to heighten its potential for toxic effects.
Research
Clinical Evidence
Low confidenceN/A
Transparency
Dusting Analysis
MEA O-Phenylphenate is not an active ingredient commonly associated with 'dusting' due to its primary role as a preservative and its regulatory status, rendering concentration optimization for efficacy irrelevant in cosmetic contexts.
The Formula
Formulation
Stability
Direct stability data for MEA O-Phenylphenate is not specified. However, related o-phenylphenate salts are known to dissociate to o-phenylphenol (the free acid) within the common environmental pH range of 4 to 9. O-phenylphenol itself demonstrates stability at pH 5, 7, and 9.
Conflicts
- Prohibited for use as a preservative in cosmetic products within the European Union due to safety concerns and regulatory mandates (effective September 17, 2019).
- As a monoalkanolamine salt, its inclusion is subject to general EU cosmetic regulations governing monoalkylamines and monoalkanolamines, which restrict the total secondary amine content to a maximum of 0.5% in ready-for-use cosmetic preparations.
Safety
Safety Profile
MEA O-Phenylphenate is banned as a cosmetic preservative in the EU since September 17, 2019. Regulatory bodies, such as the SCCS, have been unable to establish safe use levels, citing insufficient relevant data. Concerns are heightened by its demonstrated greater skin penetration and the potential for increased toxicity compared to o-phenylphenol, partly attributed to the MEA moiety.
Your Skin
Skin Compatibility
Our Assessment
Verdict
MEA O-Phenylphenate is a prohibited cosmetic ingredient in the EU with high irritancy potential and unresolved safety concerns, making it unsuitable for skincare formulations.
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