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DIHYDROXYACETONE
Chemical structure of DIHYDROXYACETONE

DIHYDROXYACETONE

CAS 96-26-4 · active · EC 202-494-5 · KR 다이하이드록시아세톤

Caution5 citations

1,3-Dihydroxyacetone

DIHYDROXYACETONE is an active ingredient used in skincare formulations.

self-tanning agent — reacts with surface skin proteins to temporarily darken skin
⚠️ Data is provided for informational purposes only. It may contain inaccuracies and should be independently verified. This is not medical advice. Consult a healthcare professional before making health decisions.

Quick facts

Description: DIHYDROXYACETONE — self-tanning agent — reacts with surface skin proteins to temporarily darken skin.

All Functions: self-tanning agent — reacts with surface skin proteins to temporarily darken skin

Quick Facts:

  • Category: active
  • Regulatory Note: Restricted in the EU

Proven Benefits At A Glance:

  • DHA is a 3-carbon sugar approved by the FDA as a color additive in sunless tanning products
  • It works by reacting with proteins in your skin to create a brown color, not by protecting from sun damage
  • DHA offers minimal to no protection against UV radiation—it’s purely cosmetic
  • The FDA recommends avoiding contact with eyes, lips, and mucous membranes, and warns against ingestion or inhalation
  • Contact dermatitis (skin irritation and allergic reactions) has been reported with DHA
  • At low concentrations used in consumer products, DHA doesn’t kill skin cells but does trigger cellular stress responses

Chemical Overview

Dihydroxyacetone is a ketotriose consisting of acetone bearing hydroxy substituents at positions 1 and 3. The simplest member of the class of ketoses and the parent of the class of glycerones. It has a role as a metabolite, an antifungal agent, a mouse metabolite, a Saccharomyces cerevisiae metabolite, an Escherichia coli metabolite and a human metabolite. It is a primary alpha-hydroxy ketone and a ketotriose. Dihydroxyacetone is a metabolite found in or produced by Escherichia coli (strain K12, MG1655). dihydroxyacetone has been reported in Arabidopsis thaliana, Homo sapiens, and other organisms with data available.

Source(s): ChEBI, E. coli Metabolome Database (ECMDB), LOTUS – the natural products occurrence database, via PubChem

Comedogenicity

No data yet
Not rated for this ingredient yet.

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