Skip to Content
Merck
All Photos(1)

Key Documents

W383902

Sigma-Aldrich

Farnesene, mixture of isomers

stabilized

Synonym(s):

(3E,6E)-3,7,11-trimethyldodeca-1,3,6,10-tetraene

Sign Into View Organizational & Contract Pricing


About This Item

Empirical Formula (Hill Notation):
C15H24
Molecular Weight:
204.35
FEMA Number:
3839
MDL number:
UNSPSC Code:
12164502
PubChem Substance ID:
Flavis number:
1.040
NACRES:
NA.21

biological source

synthetic

Quality Level

grade

Fragrance grade
Halal
Kosher

Agency

follows IFRA guidelines

reg. compliance

EU Regulation 1223/2009
FDA 21 CFR 117

form

liquid

may contain

<0.10% alpha-tocopherol, synthetic as stabilizer

composition

May include trans-β-Farnesene, cis-α-Farnesene, trans-α-Farnesene, bisabolene (a cyclic sesquiterpene), and other compounds.

color

colorless to light yellow

refractive index

n20/D 1.490-1.505 (lit.)

bp

260 °C (lit.)

density

0.844-0.8790 g/mL at 25 °C (lit.)

application(s)

flavors and fragrances

Documentation

see Safety & Documentation for available documents

food allergen

no known allergens

fragrance allergen

no known allergens

Organoleptic

lavender; citrus; herbaceous

storage temp.

2-8°C

SMILES string

C\C(C)=C\CC\C(C)=C\C\C=C(/C)C=C

InChI

1S/C15H24/c1-6-14(4)10-8-12-15(5)11-7-9-13(2)3/h6,9-10,12H,1,7-8,11H2,2-5H3/b14-10+,15-12+

InChI key

CXENHBSYCFFKJS-VDQVFBMKSA-N

Looking for similar products? Visit Product Comparison Guide

Related Categories

General description

Farnesene (mixture of isomers) may contain sequiterpenes, trans-β-farnesene, cis-α-farnesene, trans-α-farnesene, and bisabolene. α-Farnesene is reported to be an oviposition stimulant for Laspeyresia pomonella, while trans-β-farnesene as a feeding stimulant for Lutzomyia longipalpis.

Biochem/physiol Actions

Odor at 1.0%
Taste at 10-20 ppm

Other Notes

Natural occurrence: Apple, orange, grapefruit juice, mandarin and lime peel, grape, pear, ginger, nutmeg and basil.

Disclaimer

For R&D or non-EU Food use. Not for retail sale.

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Sandrine Demanèche et al.
Plants (Basel, Switzerland), 9(8) (2020-08-17)
Downy mildew of grapevine is one of the most destructive grapevine diseases worldwide. Nowadays, downy mildew control relies almost exclusively on the use of chemical pesticides, including copper products, which are efficient but controversial due to their environmental toxicity. Natural
?-Farnesene in the natural coating of apples.
Huelin FE & Murray KE.
Nature, 210(5042), 1260-1261 (1966)
Trans-beta-farnesene as a feeding stimulant for the sand fly Lutzomyia longipalpis (Diptera: Psychodidae).
Tesh RB, et al.
Journal of Medical Entomology, 29(2), 226-231 (1992)
Peng-Fei Lu et al.
Scientific reports, 10(1), 13658-13658 (2020-08-14)
The oriental fruit moth (OFM), Cydia (= Grapholitha) molesta, is a highly damaging pest; peaches are its primary host, and pears serve as post-peach secondary hosts during the late season in China. We collected volatiles from detached peach shoots and fruits
?-Farnesene, a naturally occurring oviposition stimulant for the codling moth, Laspeyresia pomonella.
Wearing CH & Hutchins RFN.
Journal of Insect Physiology, 19(6), 1251-1256 (1973)

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service