How we scored it
Where it comes from
Dominant route degrades sclareol from clary sage (Salvia sclarea) to sclareolide, reduces it to a diol and cyclises it to ambroxide; a fermentation route via sugarcane farnesene and homofarnesol is also used. Fully petrochemical syntheses from small terpenoid blocks are uncommon.
In plain English
A woody, amber-smelling fragrance molecule (ambroxide) that gives perfumes warmth and long-lasting depth. It is most often made from sclareol, a compound extracted from clary sage, or by fermentation of sugar. It is used in place of ambergris, a rare material from sperm whales.
Structure
3a,6,6,9a-tetramethyl-2,4,5,5a,7,8,9,9b-octahydro-1H-benzo[e][1]benzofuran
References
- 1ISO 16128-1:2016 and ISO 16128-2:2017 — Guidelines on technical definitions and criteria for natural and organic cosmetic ingredients and products. ISO, Geneva.
- 2Dodecahydro-Tetramethylnaphthofuran. PubChem CID 107166. National Center for Biotechnology Information. pubchem.ncbi.nlm.nih.gov ↗
- 3DODECAHYDRO-TETRAMETHYLNAPHTHOFURAN. CosIng — European Commission cosmetic ingredient database. ec.europa.eu/cosing ↗
- 4DODECAHYDRO-TETRAMETHYLNAPHTHOFURAN. CosIng u2014 European Commission database for information on cosmetic substances and ingredients. https://ec.europa.eu/growth/tools-databases/cosing/search?search=DODECAHYDRO-TETRAMETHYLNAPHTHOFURAN