Methyl Cyclopentenolone
| Category | SWEETS AND GOURMAND SMELLS |
| Subcategory | gourmand · caramel · maple |
| Origin | |
| Volatility | Heart Note |
| Botanical | N/A — synthetic molecule |
| Appearance | Colorless to pale yellow crystalline solid |
| Producing Countries | Synthesized worldwide |
| Pyramid | Heart |
Sweet, maple-caramel with a warm, fenugreek-like quality. Methyl cyclopentenolone smells like maple syrup drizzled on warm toast — deeply sweet, warm, unmistakably gourmand.
Scent
Evolution over time
Immediately
After a few hours
After a few days
The Full Story
Did You Know?
Extraction & Chemistry
Extraction method: Produced synthetically from cyclotene derivatives. Found naturally in coffee, maple syrup, and fenugreek but not commercially extracted from these sources.
| Molecular Formula | C6H8O2 |
| CAS Number | 80-71-7 |
| Botanical Name | N/A — synthetic molecule |
| IFRA Status | No known restrictions |
| Synonyms | Cyclotene, Corylone, 2-Hydroxy-3-methyl-2-cyclopenten-1-one |
| Physical Properties | |
| Lasting Power | 6–12 hours |
| Appearance | Colorless to pale yellow crystalline solid |
| Boiling Point | 200.00 °C. @ 760.00 mm Hg |
| Flash Point | > 200.00 °F. TCC ( > 93.33 °C. ) |
| Melting Point | 104.00 to 108.00 °C. @ 760.00 mm Hg |
In Perfumery
Trace modifier in gourmand and maple-themed compositions. Methyl cyclopentenolone provides maple-syrup character at extremely low concentrations (0.001-0.05%). Used in maple accords, caramel compositions, and sweet-gourmand blends. The molecule's potency limits dosage — overdosing creates an artificial, candy-like result.