Methanone, (2,4-dihydroxyphenyl)phenyl- (CAS 131-56-6) — Woody Base Note Fragrance Ingredient
Methanone, (2,4-dihydroxyphenyl)phenyl-
CAS 131-56-6
What Is Methanone, (2,4-dihydroxyphenyl)phenyl-?
This synthetic ingredient is a specialized fragrance compound primarily used in sunscreens and UV-protective cosmetics. It serves dual purposes as both a UV filter and fragrance component. Its importance lies in providing photostability to fragrances while contributing subtle aromatic qualities that enhance product formulations.
Safety Profile
USE WITH AWARENESSWhat Does Methanone, (2,4-dihydroxyphenyl)phenyl- Smell Like?
Presents a faint phenolic character with dry, slightly medicinal undertones. The aroma evolves from an initial sharpness to a more rounded, skin-like warmth. In dry-down, it leaves a subtle powdery trace reminiscent of sun-warmed cotton. Works best as a background fixative rather than a primary scent note.
In Famous Fragrances
Fragrance associations may not reflect actual formulations.
Used as a photostabilizer in this tropical floral, allowing citrus top notes to maintain brightness under UV exposure while contributing subtle phenolic depth.
Chemistry, Properties & Perfumer Guide
The Chemistry
A diaryl ketone derivative with strong UV absorption properties. Synthesized through Friedel-Crafts acylation of resorcinol. The hydroxyl groups provide both UV protection and limited solubility in polar solvents. Lacks chirality due to its symmetrical structure.
Physical & Chemical Properties
| Melting Point | 142-144 °C |
|---|
Perfumer Guide
| Application | Typical % | Range | Notes |
|---|---|---|---|
| Sunscreen Fragrances | 0.5-2% | Up to 3% | Primarily for UV stabilization |
| Functional Fragrances | 0.1-0.5% | Up to 1% | Background fixative |
Classic Accords
Tip: Combine with citrus oils to counteract phenolic notes while enhancing UV protection.
Alternatives & Comparisons
Higher UV absorption but stronger odor profile. Preferred when maximum sun protection is needed despite aromatic tradeoffs.
Safety, Regulatory & Sustainability
⚠ Regulatory Disclaimer
General reference only. Consult current IFRA Standards Library before formulating.
IFRA Status
Not currently restricted by IFRA
GHS Classification
RIFM Assessment
Evaluated as safe at current use levels in photoprotective products.
Sustainability
Synthetic production minimizes environmental impact compared to natural UV absorbers. Energy-efficient manufacturing process with high yield. Does not bioaccumulate.
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References
- Cosmetic Ingredient Review (2012). Safety Assessment of Benzophenones. Journal of Cosmetic Science.
Data: PubChem (NIH), PubMed, RIFM, IFRA. Last reviewed: Apr 2026.
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