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farnesol

cosmetic, flavor and fragrance agents
2D:
3D:
CAS Number: 4602-84-0
ECHA EC Number: 225-004-1
FDA UNII: EB41QIU6JL
CoE Number: 78
Category: cosmetic, flavor and fragrance agents
IUPAC Name: farnesol
InChI : InChI=1/C15H26O/c1-13(2)7-5-8-14(3)9-6-10-15(4)11-12-16/h7,9,11,16H,5-6,8,10,12H2,1-4H3
Std.InChI: InChI=1S/C15H26O/c1-13(2)7-5-8-14(3)9-6-10-15(4)11-12-16/h7,9,11,16H,5-6,8,10,12H2,1-4H3
InChIKey : CRDAMVZIKSXKFV-UHFFFAOYAI
Std.InChIKey: CRDAMVZIKSXKFV-UHFFFAOYSA-N
SMILES : CC(=CCCC(=CCCC(=CCO)C)C)C
MDL: MFCD00002918
Molar Refractivity : 72.77 ± 0.3 cm3 (est)
Parachor : 585.8 ± 4.0 cm3 (est)
Index of Refraction : 1.485 ± 0.02 (est)
Surface Tension : 30.3 ± 3.3 dyne/cm (est)
Density : 0.875 ± 0.06 g/cm3 (est)
Polarizability : 28.85 ± 0.5 10-24cm3 (est)
Fragrance Demo Formulas

US / EU / FDA / JECFA / FEMA / FLAVIS / Scholar / Patent Information:

Google Scholar:Search
Google Books:Search
Google Scholar: with word "volatile"Search
Google Scholar: with word "flavor"Search
Google Scholar: with word "odor"Search
Perfumer and Flavorist:Search
Google Patents:Search
US Patents:Search
EU Patents:Search
Pubchem Patents:Search
PubMed:Search
NCBI:Search
JECFA Food Flavoring:1230 farnesol
DG SANTE Food Flavourings:02.029 3,7,11-trimethyl-2,6,10-dodecatrien-1-ol
FEMA Number:2478 farnesol
FDA:No longer provide for the use of these seven synthetic flavoring substances
FDA Mainterm (SATF):4602-84-0 ; FARNESOL
FDA Regulation:
FDA PART 172 -- FOOD ADDITIVES PERMITTED FOR DIRECT ADDITION TO FOOD FOR HUMAN CONSUMPTION
Subpart F--Flavoring Agents and Related Substances
Sec. 172.515 Synthetic flavoring substances and adjuvants.

Physical Properties:

Appearance:colorless to pale yellow clear oily liquid (est)
Assay: 96.00 to 100.00 sum of isomers
Food Chemicals Codex Listed: Yes
Specific Gravity:0.88400 to 0.88900 @ 25.00 °C.
Pounds per Gallon - (est).: 7.356 to 7.397
Refractive Index:1.48700 to 1.49200 @ 20.00 °C.
Boiling Point: 149.00 °C. @ 4.00 mm Hg
Boiling Point: 263.00 °C. @ 760.00 mm Hg
Vapor Pressure:0.000370 mmHg @ 25.00 °C. (est)
Vapor Density:>1 ( Air = 1 )
Flash Point: 205.00 °F. TCC ( 96.11 °C. )
logP (o/w): 4.828 (est)
Shelf Life: 12.00 month(s) or longer if stored properly.
Storage:store in cool, dry place in tightly sealed containers, protected from heat and light.
Soluble in:
alcohol
water, 1.287 mg/L @ 25 °C (est)
Insoluble in:
water
Stability:
cream
hair spray
lipstick
lotion
non-discoloring in most media
powder
soap

Suppliers:

Associate Allied Chemicals
Farnesol P
About
Augustus Oils
Farnesol
Services
Aurochemicals
FARNESOL, Natural
Bedoukian Research
FARNESOL
≥96.0% (sum of isomers), FCC, Kosher
Odor: A delicate, fresh, green muguet note
Use: Used in rose and other floral compositions.
Flavor: Floral, woody, dry
Woody, dry notes for cranberry, tea.
Berjé
Farnesol Synthetic
Media
BOC Sciences
For experimental / research use only.
FARNESOL FCC 96.0% (sum of isomers)
Creatingperfume.com
Farnesol Symrise
Odor: Delicate, fresh, green muguet note
Diffusions Aromatiques
FARNESOL
EMD Millipore
For experimental / research use only.
Farnesol
Ernesto Ventós
FARNESOL
Odor: FLORAL, SWEET, GREEN
Excellentia International
Farnesol Natural
ExtraSynthese
For experimental / research use only.
Farnesol
Indukern F&F
FARNESOL
Odor: GREEN, FRESH, FLORAL
Jiangyin Healthway
Farnesol
New functional food ingredients
Lluch Essence
FARNESOL
Moellhausen
FARNESOL
Odor: delicate, fresh green; floral, muguet-note
Pell Wall Perfumes
Farnesol
Penta International
FARNESOL FCC
Penta International
FARNESOL
PerfumersWorld
Farnesol
Perfumery Laboratory
Farnesol Symrise
Odor: gentle, sweet, fresh fragrance with shades of lime and lily-of-the-valley flowers
Prodasynth
FARNESOL
(SUM OF ISOMERS > 96%)
Odor: FLORAL, SWEET, GREEN
Reincke & Fichtner
Farnesol
Santa Cruz Biotechnology
For experimental / research use only.
Farnesol ≥97%
Sigma-Aldrich
Farnesol, mixture of isomers, ≥95%, stabilized, FG
Odor: anise; apricot; balsam; clove; grapefruit; oily; orange; floral; peach; pear
Certified Food Grade Products
SRS Aromatics
FARNESOL
Symrise
Dragosantol®
Bisabolol and Farnesol
Odor: characteristic
Use: Dragosantol® contains at least 85 % of d,l-alpha-bisabolol, a monocyclic unsaturated sesquiterpene alcohol. Ingredients of secondary importance are mainly farnesol isomers. Dragosantol® has been shown to possess soothing properties for stressed and sensitive skin. Moreover, body odor control effectiveness has been demonstrated both for d,l-alpha-bisabolol and for Dragosantol®.Dragosantol® is suitable for use in cosmetic products due to its stability and good compatibility to the skin. The main areas of application for Dragosantol® are skin care cosmetic preparations, in particular lotions and creams for sensitive skin. Unlike Azulen or camomile oil, Dragosantol® does not alter its color after long storage periods nor diffuse through plastic containers; therefore it can be used without problems.
Symrise
Farnesol Plus
Odor: characteristic
Use: Farnesol Plus is a nature identical, synergistic complex of active ingredients with deodorising properties. Farnesol Plus is composed of Farnesol, Phenoxyethanol, Glycerine monolaurate.
Symrise
Farnesol special
Odor: very mild and delicate green floral odor with typical lily of the valley character
Use: Stable in: body lotion (very good), shampoo (good), soap (good), ap roll-on (poor), powder (poor), cleaner citric (poor), cleaner apc (very good), bleach (poor).
Flavor: sweet, flowery, juicy
Useful in: mint, fruity citrus, fruity red, fruity yellow, fruity tropical, fruity others, sweet others, alcoholics.
TCI AMERICA
For experimental / research use only.
Farnesol (mixture of isomers)
Vigon International
Farnesol

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
Pictogram
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,�-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

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

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

Potential Blenders and core components :

For Odor
aldehydic
iso
butyraldehyde
FL/FR
citronellyl oxyacetaldehyde
FL/FR
6,7,8-
decen-1-ol
FR
dodecanal (aldehyde C-12 lauric)
FL/FR
lily pentanal
FR
2-
methyl undecanal (aldehyde C-12 mna)
FL/FR
3-
methyl-4-hexyl oxybutyraldehyde
FR
muguet undecadienal
FR
nonanal (aldehyde C-9)
FL/FR
10-
undecenal (aldehyde C-11 undecylenic)
FL/FR
iso
valeraldehyde
FL/FR
amber
angelica root oil
FL/FR
cistus ladaniferus resinoid
FL/FR
animal
para-
cresyl isobutyrate
FL/FR
para-
cresyl phenyl acetate
FL/FR
indole
FL/FR
anise
anise seed oil colombia
FL/FR
anisic
para-
anisaldehyde
FL/FR
ocimum basilicum herb oil
FL/FR
balsamic
iso
amyl benzoate
FL/FR
amyris wood oil
FL/FR
siam
benzoin resinoid
FL/FR
benzophenone
FR
benzyl salicylate
FL/FR
iso
butyl cinnamate
FL/FR
cinnamyl alcohol
FL/FR
cinnamyl butyrate
FL/FR
cinnamyl formate
FL/FR
clover nitrile
FR
copaiba balsam oil
FL/FR
ethyl cinnamate
FL/FR
fir balsam absolute
FR
linalyl cinnamate
FL/FR
methyl cinnamate
FL/FR
3-
phenyl propyl alcohol
FL/FR
tolu balsam
FL/FR
berry
raspberry ketone
FL/FR
caramellic
ethyl maltol
FL/FR
immortelle absolute
FL/FR
chemical
propyl propionate
FL/FR
chocolate
iso
amyl phenyl acetate
FL/FR
citrus
benzyl anthranilate
FR
bergamot oil
FL/FR
bergamot oil bergaptene reduced italy
FL/FR
bergamot oil turkey
FL/FR
citral
FL/FR
citral dimethyl acetal
FL/FR
citrus floral green fragrance
FR
citrus ocimenol
FR
(Z)-4-
decenal
FL/FR
2,4-
dimethyl-3-cyclohexene-1-methanyl acetate
FR
grapefruit pentanol
FR
myrmac aldehyde
FR
nonanal dimethyl acetal
FL/FR
sweet
orange peel oil c.p. brazil
FL/FR
(E)-2-
tetradecenal
FL/FR
2-
tetradecenal
FL/FR
tetrahydromyrcenol
FR
earthy
2-
octanone oxime
FR
octyl phenyl acetate
FL/FR
fatty
2-
decenal
FL/FR
floral
acetaldehyde dibutyl acetal
FL/FR
amyl benzoate
FL/FR
alpha-
amyl cinnamaldehyde
FL/FR
alpha-
amyl cinnamaldehyde dimethyl acetal
FL/FR
amyl salicylate
FL/FR
iso
amyl salicylate
FL/FR
anisyl propanal / methyl anthranilate schiff's base
FR
benzyl acetate
FL/FR
bois de rose oil brazil
FL/FR
boronia concrete
FL/FR
alpha-
butyl cinnamaldehyde
FL/FR
4-iso
butyl cyclohexane propanal
FR
iso
butyl salicylate
FL/FR
citronellol
FL/FR
citronellyl acetate
FL/FR
citronellyl ethoxalate
FR
citronellyl formate
FL/FR
citronellyl propionate
FL/FR
coranol (Firmenich)
FR
coriander seed oil
FL/FR
coriander seed oil CO2 extract
FL/FR
para-
cresyl propionaldehyde
CS
cumin carbinol
FR
cyclamen aldehyde
FL/FR
cyclamen aldehyde / methyl anthranilate schiff's base
FR
cyclamen homoaldehyde
FR
cyclohexyl ethyl alcohol
FL/FR
cyclohexyl propanol
FR
2-
decalinol
FR
9-
decen-1-ol
FL/FR
dictamnus hispanicus oil
FR
dihydrocarvyl acetate
FL/FR
(±)-2,3-
dihydrofarnesol
FL/FR
dihydroisojasmonate methyl ester
FR
dihydrojasmone
FL/FR
dihydrolinalool
FL/FR
dimethyl anthranilate
FL/FR
dimethyl benzyl carbinol
FL/FR
dimethyl benzyl carbinyl acetate
FL/FR
dimethyl benzyl carbinyl butyrate
FL/FR
6,8-
dimethyl-2-nonanol
FR
3,6-
dimethyl-3-octanol
FL/FR
4-
ethyl cyclohexane propanal
FR
ethyl linalool
FR
ethyl linalyl acetal
FR
ethyl linalyl acetate
FR
ethyl linalyl ether
FL/FR
ethyl phenoxyacetate
FR
farnesyl acetate
FL/FR
floral butanal
FR
floral pyranol
FR
floral undecenone
FR
freesia acetate
FR
gardenia absolute
FR
gardenia acetal
FR
gardenia concrete
FR
gardenia decalone
FR
geraniol
FL/FR
geranium oil
FL/FR
geranium oil africa
FL/FR
geranium oil bourbon
FL/FR
geranyl acetate
FL/FR
geranyl acetone
FL/FR
geranyl formate
FL/FR
geranyl isobutyrate
FL/FR
geranyl nonanoate
CS
hawthorn ethanol
FR
heliotropyl acetone
FL/FR
(Z)-4-
hepten-2-yl salicylate
FR
(Z)-3-
hexen-1-yl salicylate
FL/FR
alpha-
hexyl cinnamaldehyde
FL/FR
hexyl lactate
FL/FR
ho leaf oil
FR
ho wood oil
FR
hyacinth ether
FR
hyacinth oil
FR
hydrangea fragrance
FR
hydroxycitronellal
FL/FR
hydroxycitronellal / methyl anthranilate schiff's base
FR
hydroxycitronellal diethyl acetal
FL/FR
hydroxycitronellal dimethyl acetal
FL/FR
hydroxycitronellal propylene glycol acetal
FL/FR
hydroxycitronellol
FL/FR
jasimia
FR
jasmin cyclopentanol
FR
jonquil absolute
FR
leerall
FR
leerall / methyl anthranilate schiff's base
FR
lilac absolute
FR
lily fragrance
FR
lily propanol
FR
lilyall
FR
lilyall / methyl anthranilate schiff's base
FR
laevo-
linalool
FL/FR
dextro-
linalool
FL/FR
linalool
FL/FR
linalool oxide
FL/FR
linalyl anthranilate
FL/FR
linalyl benzoate
FL/FR
linalyl phenyl acetate
FL/FR
linalyl propionate
FL/FR
lotus fragrance
FR
magnolia cyclohexanol
FR
magnolia decadienal
FR
magnolia indene
FR
(2-
methoxy-1-methyl propyl) benzene
FR
(3-
methoxy-2-methyl propyl) benzene
FR
methoxycitronellal
FR
1-(2-
methyl allyl oxy)-2-methyl butane
FR
4-
methyl cyclohexane propanal
FR
methyl dihydrojasmonate
FL/FR
2-
methyl octanal
FL/FR
mimosa absolute
FL/FR
mimosa absolute france
FL/FR
mimosa absolute india
FL/FR
muguet butanal
FR
muguet butanol
FR
muguet carbaldehyde
FR
muguet carbinol
FL/FR
muguet carboxaldehyde
FR
muguet dienal
FR
muguet ethanol
FR
muguet nitrile
FR
muguet octadienol
FR
muguet propanol
FR
muguet shiseol
FL/FR
nerol
FL/FR
neroli oil bigarde
FL/FR
neroli oil CO2 extract
FL/FR
nerolidol
FL/FR
(E)-
nerolidol
FL/FR
neryl acetate
FL/FR
ocean propanal
FL/FR
ocean propanal / methyl anthranilate schiff's base
FR
beta-
ocimene
FL/FR
(Z)-beta-
ocimene
FL/FR
orange leaf absolute
FL/FR
bitter
orangeflower absolute tunisia
FL/FR
orchid specialty
FR
orris pyridine 25% IPM
FR
palmarosa oil
FL/FR
papaya isobutyrate
FL/FR
peony alcohol
FR
petitgrain lemon oil
FL/FR
petitgrain oil paraguay
FL/FR
phenethyl acetate
FL/FR
phenethyl alcohol
FL/FR
phenethyl butyrate
FL/FR
phenethyl phenyl acetate
FL/FR
phenyl acetaldehyde dicitronellyl acetal
FR
phenyl acetaldehyde diisobutyl acetal
FL/FR
phenyl glycol diacetate
FR
2-
phenyl propionaldehyde ethylene glycol acetal
FR
4-
propyl cyclohexane propanal
FR
rhodinol
FL/FR
rhodinyl formate
FL/FR
rose absolute pentanol
FR
rose butanoate
FL/FR
(Z)-
rose oxide
FL/FR
laevo-
rose oxide
FL/FR
rose pyran
FR
styralyl formate
FL/FR
sweet pea absolute
FR
alpha-
terpinyl anthranilate
FL/FR
terpinyl isobutyrate
FL/FR
tetrahydrolinalool
FL/FR
5-
tricyclodecenyl acetate
FR
verdyl acetate
FR
violet methyl carbonate
FR
ylang ylang flower oil
FL/FR
ylang ylang flower oil III
FL/FR
fresh
3-(3-
propen-2-yl phenyl) butanal
FR
fruity

Occurrence (nature, food, other):

ambrette seed
Search Trop Picture
ambrette seed concrete @ 0.22%
Data GC Search Trop Picture
anise seed oil star china @ 0.03%
Data GC Search Trop Picture
basil plant
Search Trop Picture
beet oil
Search Trop Picture
bergamot oil @ trace%
Data GC Search Trop Picture
blueberry fruit
Search Trop Picture
brandy
Search PMC Picture
cabreuva
Search Trop Picture
cananga odorata oil java @ 1.24%
Data GC Search Trop Picture
cananga oil china @ 0.21%
Data GC Search Trop Picture
cassia plant
Search Trop Picture
chamomile garden chamomile plant
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chamomile sweet false chamomile plant
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cinnamon ceylon cinnamon bark
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cinnamon ceylon cinnamon leaf oil
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cinnamon ceylon cinnamon stem bark
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citronella
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clove bud oil @ 0.77%
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clove leaf oil @ 0.61%
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clove stem oil india @ 0.47%
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couroupita guianensis aubl. flower oil brazil @ 1.80%
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cranberry fruit
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cubeb oil @ trace%
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cumin fruit
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cumin seed
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davana oil @ 0.5%
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geranium rose-scented oil (pelargonium spp.) cuba @ 0.40%
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ginger rhizome oil
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ginger root
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grapefruit oil california @ 0.12%
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guava fruit oil reunion @ 0.40%
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herniaria incana lam. oil greece @ 0.80%
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jasmin absolute concrete india @ 0.22-0.44%
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lavender oil france @ trace%
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lavender oil spike spain @ 0.03%
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lemongrass plant
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neroli bigarde oil france @ trace%
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neroli oil CO2 extract @ 0.44%
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orangeflower absolute morocco @ 3.6-15.4%
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orangeflower water absolute @ 0.0-1.9%
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oregano shoot
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osmanthus absolute @ 0.18%
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palmarosa
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plumcot fruit
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raspberry red raspberry plant
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rose absolute morocco @ 0.60%
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sage plant
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sideritis scardica l. oil bulgaria @ 4.30%
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sideritis syriaca l. oil bulgaria @ 3.40%
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spearmint leaf
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tea leaf
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thyme oil wild or creeping france @ 1.92%
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tolu balsam
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turmeric root oil hydrodistilled @ 0.14%
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wine
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ylang ylang
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zingiber officinale root oil china @ 0.34%
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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

Articles:

PubMed:Effects of farnesol and the off-flavor derivative geosmin on Streptomyces tendae.
PubMed:Changes in volatile compound composition of Antrodia camphorata during solid state fermentation.
PubMed: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.
PubMed:Differential neural responses evoked by orthonasal versus retronasal odorant perception in humans.
PubMed:Characterization of the odor-active volatiles in citrus Hyuganatsu (Citrus tamurana Hort. ex Tanaka).
PubMed:Development of a multianalyte method based on micro-matrix-solid-phase dispersion for the analysis of fragrance allergens and preservatives in personal care products.
PubMed:Assessment of the antioxidant and antiproliferative effects of sesquiterpenic compounds in in vitro Caco-2 cell models.
PubMed:A new source of elemol rich essential oil and existence of multicellular oil glands in leaves of the Dioscorea species.
PubMed:Hepatoprotection of sesquiterpenoids: a quantitative structure-activity relationship (QSAR) approach.
PubMed:Characterization of essential oil from Citrus aurantium L. flowers: antimicrobial and antioxidant activities.
PubMed:Determination of E,E-farnesol in Makgeolli (rice wine) using dynamic headspace sampling and stir bar sorptive extraction coupled with gas chromatography-mass spectrometry.
PubMed:Anti-inflammatory effects of 27 selected terpenoid compounds tested through modulating Th1/Th2 cytokine secretion profiles using murine primary splenocytes.
PubMed:β-ionone induces cell cycle arrest and apoptosis in human prostate tumor cells.
PubMed:Novel antibiofilm chemotherapy targets exopolysaccharide synthesis and stress tolerance in Streptococcus mutans to modulate virulence expression in vivo.
PubMed:Chemoprevention of hepatocarcinogenesis with dietary isoprenic derivatives: cellular and molecular aspects.
PubMed:Analgesic potential of intrathecal farnesyl thiosalicylic acid and GW 5074 in vincristine-induced neuropathic pain in rats.
PubMed:Identification, functional characterization, and regulation of the enzyme responsible for floral (E)-nerolidol biosynthesis in kiwifruit (Actinidia chinensis).
PubMed:Alcohol-based quorum sensing plays a role in adhesion and sliding motility of the yeast Debaryomyces hansenii.
PubMed:Food components with anticaries activity.
PubMed:Increasing intake of long-chain n-3 PUFA enhances lipoperoxidation and modulates hepatic gene expression in a dose-dependent manner.
PubMed:Farnesol, an isoprenoid, improves metabolic abnormalities in mice via both PPARα-dependent and -independent pathways.
PubMed:Changes in volatile compound composition of Antrodia camphorata during solid state fermentation.
PubMed:Chemical composition, cytotoxicity effect and antimicrobial activity of Ceratonia siliqua essential oil with preservative effects against Listeria inoculated in minced beef meat.
PubMed:Development of a novel PPARγ ligand screening system using pinpoint fluorescence-probed protein.
PubMed:Effect of Matricaria chamomilla L. flower essential oil on the growth and ultrastructure of Aspergillus niger van Tieghem.
PubMed:In vivo and in vitro skin absorption of lipophilic compounds, dibutyl phthalate, farnesol and geraniol in the hairless guinea pig.
PubMed:d-δ-Tocotrienol-mediated suppression of the proliferation of human PANC-1, MIA PaCa-2, and BxPC-3 pancreatic carcinoma cells.
PubMed:Fragrance material review on farnesol.
PubMed:Biphenylalkylacetylhydroquinone ethers suppress the proliferation of murine B16 melanoma cells.
PubMed:Electrochemical impedance spectroscopy for the study of juvenile hormones-recombinant protein interactions.
PubMed: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.
PubMed:Effect of a short contact time with lees on volatile composition of Airen and Macabeo wines.
PubMed: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.
PubMed:Differential neural responses evoked by orthonasal versus retronasal odorant perception in humans.
PubMed:Chemical compounds of the foraging recruitment pheromone in bumblebees.
PubMed:Some advances in the knowledge of grape, wine and distillates chemistry as achieved by mass spectrometry.
PubMed:Modulation of hepatic and renal drug metabolizing enzyme activities in rats by subchronic administration of farnesol.
PubMed:Stir bar sorptive extraction applied to volatile constituents evolution during Vitis vinifera ripening.
PubMed:Studies of the isoprenoid-mediated inhibition of mevalonate synthesis applied to cancer chemotherapy and chemoprevention.
PubMed:Sensitization of Staphylococcus aureus and Escherichia coli to antibiotics by the sesquiterpenoids nerolidol, farnesol, bisabolol, and apritone.
PubMed:Juvenile hormone biosynthesis in larval and adult stick insects, Carausius morosus.
PubMed:Characterization of the odor-active volatiles in citrus Hyuganatsu (Citrus tamurana Hort. ex Tanaka).
PubMed:Influence of plant growth stage on the essential oil content and composition in Davana (Artemisia pallens wall.).
PubMed:[Reproductive and developmental toxicity study of prednisolone farnesylate (PNF)--study of subcutaneous administration of PNF during the perinatal and lactation periods in rats].
PubMed:[Reproductive and developmental toxicity study of prednisolone farnesylate (PNF)--teratogenicity study in rabbits by subcutaneous administration].
PubMed:[Reproductive and developmental toxicity study of prednisolone farnesylate (PNF)--study by subcutaneous administration of PNF during the period of fetal organogenesis in rats].
PubMed:[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].
PubMed:Activity of the corpora allata of adult female Leucophaea maderae: effects of mating and feeding.
PubMed:[The effect of a controlled gas atmosphere on farnesene dynamics and the development of sunburn in apples].
PubMed:Model studies in terpene biosynthesis.
PubMed: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.
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