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General Material Information

Preferred name farnesol
Trivial Name Farnesol
Short Description 3,7,11-trimethyl-2,6,10-dodecatrien-1-ol
Formula C15 H26 O
CAS Number 4602-84-0
FEMA Number 2478
ECHA Number 225-004-1
FDA UNII EB41QIU6JL
Beilstein Number 1763926
MDL MFCD00002918
COE Number 78
xLogP3-AA 4.80 (est)
Bio Activity Summary External link
NMR Predictor External link
JECFA Food Flavoring 1230 farnesol
FDA Patent No longer provide for the use of these seven synthetic flavoring substances
FDA Mainterm 4602-84-0 ; FARNESOL
Synonyms
  • 2,6,10-dodecatrien-1-ol, 3,7,11-trimethyl-
  • dragosantol (Symrise)
  • farnesol FCC
  • farnesol special
  • farnesol synthetic
  • farnesyl alcohol
  • 3,7,11-trimethyl dodeca-2,6,10-trienol
  • 3,7,11-trimethyl-2,6,10-dodecatrien-1-ol
  • 2,6,10-trimethyl-2,6,10-dodecatrien-12-ol
  • 3,7,11-trimethyl-2,6,10-dodecatrienol
  • 3,7,11-trimethyldodeca-2,6,10-trien-1-ol
  • 3,7,11-trimethyldodeca-2,6,10-trien-1-ol
  • 2,6,10-Dodecatrien-1-ol, 3,7,11-trimethyl-
  • 3,7,11-Trimethyl-2,6,10-dodecatrien-1-ol
  • FCI 119a
  • NSC 60597
  • Nikkosome
  • 3,7,11-Trimethyl-2,6,10-dodecen-1-ol
  • CSU 1806
  • MeSH ID: D005204

US / EU / FDA / JECFA / FEMA / Scholar / Patents

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Literature & References

3,7,11-trimethyldodeca-2,6,10-trien-1-ol
NIST Chemistry WebBook:Search Inchi
Canada Domestic Sub. List:4602-84-0
Pubchem (cid):3327
Pubchem (sid):134986027
Publications by PubMed
Effects of farnesol and the off-flavor derivative geosmin on Streptomyces tendae.
Changes in volatile compound composition of Antrodia camphorata during solid state fermentation.
Improved production of isoamyl acetate by a sake yeast mutant resistant to an isoprenoid analog and its dependence on alcohol acetyltransferase activity, but not on isoamyl alcohol production.
Differential neural responses evoked by orthonasal versus retronasal odorant perception in humans.
Characterization of the odor-active volatiles in citrus Hyuganatsu (Citrus tamurana Hort. ex Tanaka).
Development of a multianalyte method based on micro-matrix-solid-phase dispersion for the analysis of fragrance allergens and preservatives in personal care products.
Assessment of the antioxidant and antiproliferative effects of sesquiterpenic compounds in in vitro Caco-2 cell models.
A new source of elemol rich essential oil and existence of multicellular oil glands in leaves of the Dioscorea species.
Hepatoprotection of sesquiterpenoids: a quantitative structure-activity relationship (QSAR) approach.
Characterization of essential oil from Citrus aurantium L. flowers: antimicrobial and antioxidant activities.
Determination of E,E-farnesol in Makgeolli (rice wine) using dynamic headspace sampling and stir bar sorptive extraction coupled with gas chromatography-mass spectrometry.
Anti-inflammatory effects of 27 selected terpenoid compounds tested through modulating Th1/Th2 cytokine secretion profiles using murine primary splenocytes.
β-ionone induces cell cycle arrest and apoptosis in human prostate tumor cells.
Novel antibiofilm chemotherapy targets exopolysaccharide synthesis and stress tolerance in Streptococcus mutans to modulate virulence expression in vivo.
Chemoprevention of hepatocarcinogenesis with dietary isoprenic derivatives: cellular and molecular aspects.
Analgesic potential of intrathecal farnesyl thiosalicylic acid and GW 5074 in vincristine-induced neuropathic pain in rats.
Identification, functional characterization, and regulation of the enzyme responsible for floral (E)-nerolidol biosynthesis in kiwifruit (Actinidia chinensis).
Alcohol-based quorum sensing plays a role in adhesion and sliding motility of the yeast Debaryomyces hansenii.
Food components with anticaries activity.
Increasing intake of long-chain n-3 PUFA enhances lipoperoxidation and modulates hepatic gene expression in a dose-dependent manner.
Farnesol, an isoprenoid, improves metabolic abnormalities in mice via both PPARα-dependent and -independent pathways.
Changes in volatile compound composition of Antrodia camphorata during solid state fermentation.
Chemical composition, cytotoxicity effect and antimicrobial activity of Ceratonia siliqua essential oil with preservative effects against Listeria inoculated in minced beef meat.
Development of a novel PPARγ ligand screening system using pinpoint fluorescence-probed protein.
Effect of Matricaria chamomilla L. flower essential oil on the growth and ultrastructure of Aspergillus niger van Tieghem.
In vivo and in vitro skin absorption of lipophilic compounds, dibutyl phthalate, farnesol and geraniol in the hairless guinea pig.
d-δ-Tocotrienol-mediated suppression of the proliferation of human PANC-1, MIA PaCa-2, and BxPC-3 pancreatic carcinoma cells.
Fragrance material review on farnesol.
Biphenylalkylacetylhydroquinone ethers suppress the proliferation of murine B16 melanoma cells.
Electrochemical impedance spectroscopy for the study of juvenile hormones-recombinant protein interactions.
Evaluation of an alcohol-based surgical hand disinfectant containing a synergistic combination of farnesol and benzethonium chloride for immediate and persistent activity against resident hand flora of volunteers and with a novel in vitro pig skin model.
Effect of a short contact time with lees on volatile composition of Airen and Macabeo wines.
Farnesol and geraniol chemopreventive activities during the initial phases of hepatocarcinogenesis involve similar actions on cell proliferation and DNA damage, but distinct actions on apoptosis, plasma cholesterol and HMGCoA reductase.
Differential neural responses evoked by orthonasal versus retronasal odorant perception in humans.
Chemical compounds of the foraging recruitment pheromone in bumblebees.
Some advances in the knowledge of grape, wine and distillates chemistry as achieved by mass spectrometry.
Modulation of hepatic and renal drug metabolizing enzyme activities in rats by subchronic administration of farnesol.
Stir bar sorptive extraction applied to volatile constituents evolution during Vitis vinifera ripening.
Studies of the isoprenoid-mediated inhibition of mevalonate synthesis applied to cancer chemotherapy and chemoprevention.
Sensitization of Staphylococcus aureus and Escherichia coli to antibiotics by the sesquiterpenoids nerolidol, farnesol, bisabolol, and apritone.
Juvenile hormone biosynthesis in larval and adult stick insects, Carausius morosus.
Characterization of the odor-active volatiles in citrus Hyuganatsu (Citrus tamurana Hort. ex Tanaka).
Influence of plant growth stage on the essential oil content and composition in Davana (Artemisia pallens wall.).
[Reproductive and developmental toxicity study of prednisolone farnesylate (PNF)--study of subcutaneous administration of PNF during the perinatal and lactation periods in rats].
[Reproductive and developmental toxicity study of prednisolone farnesylate (PNF)--teratogenicity study in rabbits by subcutaneous administration].
[Reproductive and developmental toxicity study of prednisolone farnesylate (PNF)--study by subcutaneous administration of PNF during the period of fetal organogenesis in rats].
[Reproductive and developmental toxicity study of prednisolone farnesylate (PNF)--study by subcutaneous administration of PNF prior to and in the early stages of pregnancy in rats].
Activity of the corpora allata of adult female Leucophaea maderae: effects of mating and feeding.
[The effect of a controlled gas atmosphere on farnesene dynamics and the development of sunburn in apples].
Model studies in terpene biosynthesis.
Superficial scald, a functional disorder of stored apples. IV. Effect of variety, maturity, oiled wraps and diphenylamine on the concentration of alpha-farnesene in the fruit.

Other Information

(IUPAC):Atomic Weights of the Elements 2011 (pdf)
Videos:The Periodic Table of Videos
tgsc:Atomic Weights use for this web site
(IUPAC):Periodic Table of the Elements
FDA Substances Added to Food (formerly EAFUS):View
CHEBI:View
CHEMBL:View
Golm Metabolome Database:Search
KEGG (GenomeNet):C01126
HMDB (The Human Metabolome Database):HMDB04305
FooDB:FDB014891
Export Tariff Code:2905.22.5050
Typical G.C.
VCF-Online:VCF Volatile Compounds in Food
ChemSpider:View
Wikipedia:View

PhysChem Properties

Material listed in food chemical codex Yes
Molecular weight 222.37141418457
Specific gravity @ 25 °C
Pounds per Gallon 7.356 to 7.397
Refractive Index 1.487 to 1.492 @ 20 °C
Vapor Pressure 0.00037 mmHg @ 25 °C
Vapor Density 1
Flash Point TCC Value 96.11 °C TCC
logP (o/w) 4.828 est
Shelf life 12 months (or longer if stored properly.)
Storage notes Store in cool, dry place in tightly sealed containers, protected from heat and light.
Solubility
alcohol Yes
water, 1.287 mg/L @ 25 °C (est) Yes
water No
Stability
cream Unspecified
hair spray Unspecified
lipstick Unspecified
lotion Unspecified
non-discoloring in most media Unspecified
powder Unspecified
soap Unspecified

Organoleptic Properties

Odor Type: Floral
fresh, sweet, linden flower, floral, angelica, dry
Odor strength low
Substantivity 400 hour(s) at 100.00 %
Luebke, William tgsc, (1985) At 100.00 %. mild fresh sweet linden floral angelica
Flavor Type: Floral
floral, juicy, green, tropical, plum, pear, peach, cilantro, metallic
Luebke, William tgsc, (1985) Floral juicy green tropical plum pear peach cilantro metallic
Woody, dry notes for cranberry, tea. Floral, woody, dry
Useful in: mint, fruity citrus, fruity red, fruity yellow, fruity tropical, fruity others, sweet others, alcoholics. Sweet, flowery, juicy

Occurrences

Safety Information

Safety information

Preferred SDS: View
European information :
Most important hazard(s):
Xi - Irritant
R 36/38 - Irritating to skin and eyes.
R 43 - May cause sensitisation by skin contact.
S 02 - Keep out of the reach of children.
S 24/25 - Avoid contact with skin and eyes.
S 26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
S 36 - Wear suitable protective clothing.
Hazards identification
Classification of the substance or mixture
GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)
Acute aquatic toxicity (Category 2), H401
Chronic aquatic toxicity (Category 2), H411
GHS Label elements, including precautionary statements
Pictogramenvironment.jpg
Signal word Warning
Hazard statement(s)
H401 - Toxic to aquatic life
H411 - Toxic to aquatic life with long lasting effects
Precautionary statement(s)
P273 - Avoid release to the environment.
P391 - Collect spillage. Hazardous to the aquatic environment
P501 - Dispose of contents/ container to an approved waste disposal plant.
Oral/Parenteral Toxicity:
oral-rat LD50 6000 mg/kg
BEHAVIORAL: SOMNOLENCE (GENERAL DEPRESSED ACTIVITY) BEHAVIORAL: ANTIPSYCHOTIC
Therapie. Vol. 27, Pg. 893, 1972.

oral-mouse LD50 7400 mg/kg
BEHAVIORAL: SOMNOLENCE (GENERAL DEPRESSED ACTIVITY) BEHAVIORAL: ANTIPSYCHOTIC
Therapie. Vol. 27, Pg. 893, 1972.

intraperitoneal-mouse LD50 443 mg/kg
BEHAVIORAL: SOMNOLENCE (GENERAL DEPRESSED ACTIVITY) BEHAVIORAL: ANTIPSYCHOTIC
Therapie. Vol. 27, Pg. 893, 1972.

Dermal Toxicity:
skin-rabbit LD50 > 5000 mg/kg
Therapie. Vol. 27, Pg. 893, 1972.

Inhalation Toxicity:
Not determined

Safety in use information

Category:
cosmetic, flavor and fragrance agents
RIFM Fragrance Material Safety Assessment: Search
IFRA Code of Practice Notification of the 49th Amendment to the IFRA Code of Practice
IFRA Critical Effect:
Dermal sensitization
View the IFRA Standard
View IFRA Standards Library for complete information.
Please review Amendment 49 IFRA documentation for complete information.
IFRA RESTRICTION LIMITS IN THE FINISHED PRODUCT (%):
Category 1: Products applied to the lips
0.21 %
Category 2: Products applied to the axillae
0.062 %
Category 3: Products applied to the face/body using fingertips
1.20 %
Category 4: Products related to fine fragrance
1.20 %
Category 5: Products applied to the face and body using the hands (palms), primarily leave-on
Category 5A: Body lotion products applied to the body using the hands (palms), primarily leave-on
0.29 %
Category 5B: Face moisturizer products applied to the face using the hands (palms), primarily leave-on
0.29 %
Category 5C: Hand cream products applied to the hands using the hands (palms), primarily leave-on
0.29 %
Category 5D: Baby Creams, baby Oils and baby talc
0.29 %
Category 6: Products with oral and lip exposure
0.68 %
Category 7: Products applied to the hair with some hand contact
Category 7A: Rinse-off products applied to the hair with some hand contact
2.40 %
Category 7B: Leave-on products applied to the hair with some hand contact
2.40 %
Category 8: Products with significant anogenital exposure
0.12 %
Category 9: Products with body and hand exposure, primarily rinse off
2.30 %
Category 10: Household care products with mostly hand contact
Category 10A: Household care excluding aerosol products (excluding aerosol/spray products)
8.10 %
Category 10B: Household aerosol/spray products
8.10 %
Category 11: Products with intended skin contact but minimal transfer of fragrance to skin from inert substrate
Category 11A: Products with intended skin contact but minimal transfer of fragrance to skin from inert substrate without UV exposure
4.50 %
Category 11B: Products with intended skin contact but minimal transfer of fragrance to skin from inert substrate with potential UV exposure
4.50 %
Category 12: Products not intended for direct skin contact, minimal or insignificant transfer to skin
No Restriction
Notes:
IFRA FLAVOR REQUIREMENTS:

Due to the possible ingestion of small amounts of fragrance ingredients from their use in products in Categories 1 and 6, materials must not only comply with IFRA Standards but must also be recognized as safe as a flavoring ingredient as defined by the IOFI Code of Practice (www.iofi.org). For more details see chapter 1 of the Guidance for the use of IFRA Standards.

Maximised Survey-derived Daily Intakes (MSDI-EU): 7.70 (μg/capita/day)
Maximised Survey-derived Daily Intakes (MSDI-USA): 2.60 (μg/capita/day)
Threshold of Concern:1800 (μg/person/day)
Structure Class: I
Use levels for FEMA GRAS flavoring substances on which the FEMA Expert Panel based its judgments that the substances are generally recognized as safe (GRAS).
The Expert Panel also publishes separate extensive reviews of scientific information on all FEMA GRAS flavoring substances and can be found at FEMA Flavor Ingredient Library
publication number: 3
Click here to view publication 3
average usual ppmaverage maximum ppm
baked goods: -1.70000
beverages(nonalcoholic): -0.76000
beverages(alcoholic): --
breakfast cereal: --
cheese: --
chewing gum: --
condiments / relishes: --
confectionery froastings: --
egg products: --
fats / oils: --
fish products: --
frozen dairy: -0.40000
fruit ices: -0.40000
gelatins / puddings: -0.10000
granulated sugar: --
gravies: --
hard candy: -1.40000
imitation dairy: --
instant coffee / tea: --
jams / jellies: --
meat products: --
milk products: --
nut products: --
other grains: --
poultry: --
processed fruits: --
processed vegetables: --
reconstituted vegetables: --
seasonings / flavors: --
snack foods: --
soft candy: --
soups: --
sugar substitutes: --
sweet sauces: --

Safety references

European Food Safety Athority(EFSA):Flavor usage levels; Subacute, Subchronic, Chronic and Carcinogenicity Studies; Developmental / Reproductive Toxicity Studies; Genotoxicity Studies...

European Food Safety Authority (EFSA) reference(s):

Flavouring Group Evaluation 202: 3-Alkylated aliphatic acyclic alpha,beta-unsaturated aldehydes and precursors with or without additional double bonds from chemical subgroup 1.1.3 of FGE.19[1]
View page or View pdf

Flavouring Group Evaluation 72 (FGE.72): Consideration of aliphatic, branched-chain saturated and unsaturated alcohols, aldehydes, acids, and related esters evaluated by the JECFA (61st meeting) structurally related to branched- and straight-chain unsaturated carboxylic acids. Esters of these and straight-chain aliphatic saturated alcohols evaluated by EFSA in FGE.05Rev2 (2010)
View page or View pdf

Scientific Opinion on Flavouring Group Evaluation 95 (FGE.95): Consideration of aliphatic, linear or branched-chain saturated and unsaturated alcohols, aldehydes, acids and related esters evaluated by JECFA (69th meeting) structurally related to esters of branched- and straight-chain aliphatic saturated primary alcohols and of one secondary alcohol, and branched- and straight-chain unsaturated carboxylic acids evaluated by EFSA in FGE.05Rev1 (2008)
View page or View pdf

Scientific Opinion on Flavouring Group Evaluation 72, Revision 1 (FGE.72Rev1): Consideration of aliphatic, branched-chain saturated and unsaturated alcohols, aldehydes, acids, and related esters evaluated by the JECFA (61st meeting) structurally related to branched- and straight-chain unsaturated carboxylic acids, esters of these and straight-chain aliphatic saturated alcohols evaluated by EFSA in FGE.05Rev2
View page or View pdf

Safety and efficacy of a,ß-unsaturated straight-chain and branched-chain aliphatic primary alcohols, aldehydes, acids and esters belonging to chemical group 3 when used as flavourings for all animal species
View page or View pdf

Scientific Opinion on Flavouring Group Evaluation 72, Revision 2 (FGE.72Rev2): consideration of aliphatic, branched-chain saturated and unsaturated alcohols, aldehydes, acids and related esters evaluated by JECFA (61st, 68th and 69th meetings) and structurally related to flavouring substances in FGE.05Rev3
View page or View pdf

EPI System: View
AIDS Citations:Search
Cancer Citations:Search
Toxicology Citations:Search
EPA Substance Registry Services (TSCA):4602-84-0
EPA ACToR:Toxicology Data
EPA Substance Registry Services (SRS):Registry
Laboratory Chemical Safety Summary :3327
National Institute of Allergy and Infectious Diseases:Data
SCCNFP:opinion
WGK Germany:2
3,7,11-trimethyldodeca-2,6,10-trien-1-ol
Chemidplus:0004602840
EPA/NOAA CAMEO:hazardous materials
RTECS:JR4979000 for cas# 4602-84-0