Science
Mechanism of Action
Functions as a dye coupler that undergoes oxidation in the presence of hydrogen peroxide, forming quinone-imine intermediates that react with primary dye intermediates to create large polymeric pigment molecules
Research
Clinical Evidence
Medium confidenceN/A
Key findings
- 01 FDA/CIR Safety Assessment establishing 0.2% maximum concentration for hair dye use
- 02 SCCS dermal absorption study showing 0.41-1.68% skin penetration at 2% concentration
Transparency
Dusting Analysis
Not applicable to skincare formulations - this ingredient is restricted to hair dye applications only
The Formula
Formulation
Stability
Requires acidic conditions for stability; rapidly degrades in alkaline environments with darkening. Most stable as dihydrochloride salt form. Light and heat sensitive.
Conflicts
- Strong oxidizing agents
- Strong acids
- Transition metals
- Alkaline environments
Safety
Safety Profile
Known skin sensitizer and primary irritant. Prohibited for eye area use. Mutagenic potential at higher concentrations. Restricted to hair dye applications only.
Your Skin
Skin Compatibility
Our Assessment
Verdict
Not suitable for skincare applications due to high sensitization risk and restriction to hair dye use only.
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References
Sources