Science
Mechanism of Action
It acts by uncoupling oxidative phosphorylation and binding to microbial protein thiol groups. This disrupts cell membrane integrity and interferes with essential metabolic enzymes.
Research
Clinical Evidence
Insufficient-data confidenceN/A
Transparency
Dusting Analysis
The Formula
Formulation
Stability
Dichlorophene is acidic, slowly oxidizes in air, and forms salts with alkalis. Its photolysis pathways are pH and oxygen-dependent.
Conflicts
- strong oxidizing agents
- strong bases
Safety
Safety Profile
The CIR found insufficient safety data for cosmetics. Europe limits its concentration to 0.5%, Japan prohibits it, and the EPA warns of developmental toxicity.
Your Skin
Skin Compatibility
Our Assessment
Verdict
Despite its antimicrobial properties, Dichlorophene is widely restricted or prohibited in cosmetics due to significant safety concerns, including potential for sensitization and developmental toxicity.
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