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Farnesol

3,7,11-Trimethyl-2,6,10-dodecatrien-1-ol

(2E,6E)-Farnesol · trans,trans-Farnesol

Aliphatic sesquiterpenoid polyalkene alcohol · C₁₅H₂₆O

Chemical structure of Farnesol
2D structure PubChem / NCI CIR

Chemical info

CAS number CAS
106-28-5
Molecular formula
C₁₅H₂₆O
Molecular weight
222.37 g/mol
Aroma
Light floral, with lily-of-the-valley and chamomile facets, sweet and soft.

Safety

Weak sensitizer · IFRA restricted

Farnesol is a sesquiterpene alcohol occurring mainly in ambrette and Western Australian sandalwood oils. The EU lists it as one of 26 fragrance allergens requiring declaration.

Skin. A 5 percent patch test across three groups of more than 300 volunteers produced no irritation or sensitization. In maximation tests, 5 percent of healthy individuals showed allergic reactions to farnesol at 10 to 12 percent. Undiluted material caused reactions in 14.7 percent of individuals.

Dermatitis patients. Reaction rates to 5 percent farnesol vary from 0.4 to 1.2 percent in large European studies. Several cases of axillary dermatitis have been reported in young women using farnesol-containing deodorants.

Oral and dermal. Acute oral LD50 in rats exceeds 5 g/kg, in mice 8.76 g/kg. Acute dermal LD50 in rabbits exceeds 5 g/kg.

Subchronic. A 28-day oral study at 500 to 1,000 mg/kg/day in rats showed no clinical toxicity. Increased kidney and liver weights were attributed to induction of drug-metabolizing enzymes.

Mutagenicity and cancer. Not mutagenic in Ames or micronucleus tests. Significant anticancer activity against melanoma, pancreatic, leukemia and oral squamous carcinoma cells.


Usage guidelines

Concern level
Low to moderate
IFRA
1.2 percent in leave-on products, minimum 96 percent isomer purity
EU
Mandatory declaration above 100 ppm (rinse-off) or 10 ppm (leave-on)
Oils with high content
Ambrette 3.4 – 39.0 percent

Found in essential oils

Principal sources
Ambrette3.4 – 39.0 %
Sandalwood (Western Australian)7.9 – 9.3 %
Palmarosa0.5 – 6.1 %
Neroli0 – 3.2 %
Vassoura5.5 %
Rose (Japanese)3.8 %
Galangal (greater)0 – 3.1 %
Cabreuva2.5 %
Rose (Damask)0 – 1.5 %
Rose (Provence)0.5 – 1.3 %
Tuberose1.7 %

Pharmacokinetics

After oral administration of a mixture of farnesol isomers in rats, 80 percent of farnesol recovered in plasma was the (2E,6E)-isomer. A 28-day oral course significantly increased the activities of several liver enzymes including CYP1A, CYP2A1-3, CYP2B1/2, CYP2E1, CYP3A1/2, glutathione reductase and UGT.


Notes

Farnesol is sometimes used as a bacteriostat as well as a fragrance material in deodorants. The real-world risk of skin sensitization from farnesol in essential oils is low.