(+)-epi–Bisabolol (CAS 76738-75-5) — Floral Base Note Fragrance Ingredient
(+)-epi-_-Bisabolol
CAS 76738-75-5
What Is (+)-epi-_-Bisabolol?
(+)-epi-α-Bisabolol is a naturally occurring monocyclic sesquiterpene alcohol found in chamomile and other plants. It’s used in skincare for its soothing properties and in fragrances for its mild, sweet, floral-woody aroma. This ingredient matters because it combines therapeutic benefits with subtle fragrance enhancement, making it popular in ‘clean beauty’ products.
Safety Profile
GENERALLY SAFEWhat Does (+)-epi-_-Bisabolol Smell Like?
A delicate balance of floral sweetness and creamy woodiness, like chamomile tea steeping in a cedarwood box. The scent unfolds with a soft powdery nuance reminiscent of baby products, settling into a comforting skin-like warmth. Its subtlety makes it an ideal base for enhancing other notes without overpowering them.
Chemistry, Properties & Perfumer Guide
The Chemistry
(+)-epi-α-Bisabolol is a sesquiterpene alcohol with four stereocenters. The (+)-epi form differs from α-bisabolol in its stereochemistry at C7. Industrially produced via stereoselective synthesis from farnesyl derivatives or by microbial transformation. Its chirality significantly impacts both biological activity and odor profile, with the (+)-epi form being more thermally stable than other isomers.
Physical & Chemical Properties
| Molecular Weight | 222.37 g/mol |
|---|---|
| Boiling Point | 153-154°C at 12 mmHg |
| Optical Rotation | +51.5° (c=1, CHCl3) |
Perfumer Guide
| Application | Typical % | Range | Notes |
|---|---|---|---|
| Skincare Fragrance | 0.5-2% | Up to 5% | Adds subtle scent to sensitive skin products |
| Aromatherapy | 1-3% | Up to 10% | Enhances relaxation blends |
Classic Accords
Tip: Use to round off sharp edges in citrus or herbal compositions.
Alternatives & Comparisons
The more common isomer with similar properties but slightly different odor profile.
Oxidized form with reduced fragrance impact but increased stability in formulations.
Safety, Regulatory & Sustainability
⚠ Regulatory Disclaimer
General reference only. Consult current IFRA Standards Library before formulating.
IFRA Status
No restrictions. IFRA compliant without limitations.
RIFM Assessment
RIFM assessment confirms safety for current use levels in cosmetics.
Sustainability
While naturally occurring in chamomile, commercial production is typically synthetic for consistency and yield. The synthetic route reduces agricultural land use compared to plant extraction. Biocatalytic production methods are being developed to improve green chemistry metrics.
Explore (+)-epi-_-Bisabolol
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References
- PubChem Compound Summary for (+)-epi-α-Bisabolol CID 1549992
- Bickers et al. (2005). Safety assessment of bisabolols. Food Chem Toxicol. PMID 15979247
Data: PubChem (NIH), PubMed, RIFM, IFRA. Last reviewed: Apr 2026.
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