(Z,E)-farnesol
2,6,10-dodecatrien-1-ol, 3,7,11-trimethyl-, (Z,E)-
 
Notes:
None found
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CAS Number: 3790-71-4Picture of molecule3D/inchi
FDA UNII: SQ4TI19PXT
Nikkaji Web: J133.568E
Beilstein Number: 1723038
MDL: MFCD21365076
XlogP3-AA: 4.80 (est)
Molecular Weight: 222.37142000
Formula: C15 H26 O
NMR Predictor: Predict (works with chrome or firefox)
Category: flavor and fragrance agents
 
US / EU / FDA / JECFA / FEMA / FLAVIS / Scholar / Patent Information:
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Physical Properties:
Appearance: colorless to pale yellow clear liquid (est)
Assay: 92.00 to 100.00 % 
Food Chemicals Codex Listed: No
Boiling Point: 283.00 to  284.00 °C. @ 760.00 mm Hg (est)
Vapor Pressure: 0.000370 mmHg @ 25.00 °C. (est)
Flash Point: 234.00 °F. TCC ( 112.50 °C. ) (est)
logP (o/w): 5.314 (est)
Soluble in:
 alcohol
 water, 1.287 mg/L @ 25 °C (est)
Insoluble in:
 water
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Organoleptic Properties:
 
Odor and/or flavor descriptions from others (if found).
 
 
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Cosmetic Information:
None found
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Suppliers:
Sigma-Aldrich: Sigma
For experimental / research use only.
2-cis,6-trans-Farnesol ≥95.0% (GC)
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Safety Information:
Preferred SDS: View
 
Hazards identification
 
Classification of the substance or mixture
GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)
None found.
GHS Label elements, including precautionary statements
 
Pictogram
 
Hazard statement(s)
None found.
Precautionary statement(s)
None found.
Oral/Parenteral Toxicity:
Not determined
Dermal Toxicity:
Not determined
Inhalation Toxicity:
Not determined
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Safety in Use Information:
Category: flavor and fragrance agents
IFRA Code of Practice Notification of the 49th Amendment to the IFRA Code of Practice
 
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Safety References:
EPI System: View
AIDS Citations: Search
Cancer Citations: Search
Toxicology Citations: Search
EPA ACToR: Toxicology Data
EPA Substance Registry Services (SRS): Registry
Laboratory Chemical Safety Summary : 1549108
National Institute of Allergy and Infectious Diseases: Data
 (2Z,6E)-3,7,11-trimethyldodeca-2,6,10-trien-1-ol
Chemidplus: 0003790714
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References:
 (2Z,6E)-3,7,11-trimethyldodeca-2,6,10-trien-1-ol
NIST Chemistry WebBook: Search Inchi
Pubchem (cid): 1549108
Pubchem (sid): 135063463
Pherobase: View
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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
CHEBI: View
KEGG (GenomeNet): C03220
HMDB (The Human Metabolome Database): Search
FooDB: FDB014760
Export Tariff Code: 2905.22.0000
Typical G.C.
VCF-Online: VCF Volatile Compounds in Food
ChemSpider: View
Wikipedia: View
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Potential Blenders and core components note
 
None Found
 
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Potential Uses:
None Found
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Occurrence (nature, food, other): note
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Synonyms:
2,6,10-dodecatrien-1-ol, 3,7,11-trimethyl-, (Z,E)-
(2-cis,6-trans)-farnesol
(2Z,6E)-farnesol
2-cis,6-trans-farnesol
cis,trans-farnesol
(Z,E)-3,7,11-trimethyl-2,6,10-dodecatrien-1-ol
cis,trans-3,7,11-trimethyl-2,6,10-dodecatrien-1-ol
(2-cis,6-trans)-3,7,11-trimethyldodeca-2,6,10-trien-1-ol
(2Z,6E)-3,7,11-trimethyldodeca-2,6,10-trien-1-ol
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Articles:
PubMed: Synthesis of farnesol isomers via a modified Wittig procedure.
PubMed: Characterization of the odor-active volatiles in citrus Hyuganatsu (Citrus tamurana Hort. ex Tanaka).
PubMed: Lipid metabolism in helminth parasites--VI. Synthesis of 2-cis,6-trans farnesol by Hymenolepis diminuta (Cestoda).
PubMed: Determination of the volatile composition in essential oil of Descurainia sophia (L.) Webb ex Prantl (Flixweed) by gas chromatography/mass spectrometry (GC/MS).
PubMed: Effect of Matricaria chamomilla L. flower essential oil on the growth and ultrastructure of Aspergillus niger van Tieghem.
PubMed: Composition of volatile organic compounds in flowers of Astragalus sahendi.
PubMed: Engineered heterologous FPP synthases-mediated Z,E-FPP synthesis in E. coli.
PubMed: Analysis of the essential oil of Grindelia discoidea.
PubMed: Volatile constituents of redblush grapefruit (Citrus paradisi) and pummelo (Citrus grandis) peel essential oils from Kenya.
PubMed: Hydrolysis and isomerization of trans,trans-farnesyl diphosphate by Andrographis tissue-culture enzymes.
PubMed: Biosynthesis of trans, trans- and cis, trans-farnesols by soluble enzymes from tissue cultures of Andrographis paniculata.
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