Why the score varies
This ingredient is made commercially by more than one route, and ISO 16128 scores the feedstock actually used. Without a supplier certificate of origin the value cannot be claimed.
| Route | Feedstock | NOI | Share | Notes |
|---|---|---|---|---|
| Synthetic (racemic) from petrochemical terpene precursors | petrochemical farnesene/nerolidol-type intermediates | 0.00 | ~60% | |
| Steam distillation from candeia tree bark or chamomile oil | candeia wood or German chamomile essential oil | 1.00 | ~40% |
How we scored it
How it’s made
Where it comes from
A large share of commercial bisabolol is synthesised from petrochemical terpene intermediates. The natural alternative, levomenol, is steam-distilled from Brazilian candeia tree bark or German chamomile oil.
In plain English
A soothing skin-conditioning ingredient with a mild floral scent, used to calm and condition skin. It can be extracted from Brazilian candeia tree bark or chamomile oil, but much of the supply is made synthetically from petrochemical terpene chemicals.
CosIng definition: (R*,R*)-.alpha.,4-dimethyl-.alpha.-(4-methyl-3-pentenyl)cyclohex-3-ene-1-methanol; 3-Cyclohexene-1-methanol, alpha,4-dimethyl-alpha-(4-methyl-3-pentenyl)-, (theta,theta)-(+/-)-; 3-Cyclohexene-1-methanol, alpha,4-dimethyl-alpha-(4-methyl-3-pentenyl)-, (S-(theta,theta))- (levomenol)
Natural alternatives with the same function
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Structure
(2R)-6-methyl-2-[(1R)-4-methylcyclohex-3-en-1-yl]hept-5-en-2-ol
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.
- 2Bisabolol. PubChem CID 1549992. National Center for Biotechnology Information. pubchem.ncbi.nlm.nih.gov ↗
- 3BISABOLOL. CosIng — European Commission cosmetic ingredient database. ec.europa.eu/cosing ↗
- 4BISABOLOL. CosIng u2014 European Commission database for information on cosmetic substances and ingredients. https://ec.europa.eu/growth/tools-databases/cosing/search?search=BISABOLOL