Identification

Namefarnesane
IUPAC2,6,10-trimethyldodecane
CAS Number3891-98-3
FDA UNII8X81V0IT6Q
Molecular FormulaC15 H32
Molecular Weight212.42004000
MDL NumberMFCD00027077
Nikkaji NumberJ13.488K
Beilstein1719672

Regulatory

Physical Properties

Appearance colorless to pale yellow clear liquid (est)
Assay 95.00 to 100.00
Food Chemicals Codex Listed No
Boiling Point 248.00 to 250.00 °C. @ 760.00 mm Hg (est)
Vapor Pressure 0.037000 mmHg @ 25.00 °C. (est)
Flash Point 218.00 °F. TCC ( 103.10 °C. ) (est)
logP (o/w) 7.882 (est)
Soluble in alcohol
Insoluble in water

No sensory data available

Safety Information

Preferred SDSView
Oral/Parenteral ToxicityNot determined
Dermal ToxicityNot determined
Inhalation ToxicityNot determined

GHS Classification

['GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)', 'GHS Label elements, including precautionary statements']

Safety in Use

Categoryflavor and fragrance agents
RIFM Fragrance Material Safety AssessmentSearch

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Potential Uses

None Found

Natural Occurrence

walnut black walnut oil

Synonyms

dodecane, 2,6,10-trimethyl- 2,6,10- trimethyl dodecane 2,6,10- trimethyldodecane PubMed: Simultaneous determination of hydrocarbon renewable diesel, biodiesel and petroleum diesel contents in diesel fuel blends using near infrared (NIR) spectroscopy and chemometrics. PubMed: Alleviating monoterpene toxicity using a two-phase extractive fermentation for the bioproduction of jet fuel mixtures in Saccharomyces cerevisiae. PubMed: Detailed analysis of petroleum hydrocarbon attenuation in biopiles by high-performance liquid chromatography followed by comprehensive two-dimensional gas chromatography. PubMed: Biodegradation of hydrocarbon cuts used for diesel oil formulation. PubMed: New farnesane-type sesquiterpenes, hedychiols A and B 8,9-diacetate, and inhibitors of degranulation in RBL-2H3 cells from the rhizome of Hedychium coronarium. PubMed: Novel oligorhamnosides from the stem bark of Cleistopholis glauca. PubMed: Natural and synthetic materials with insect hormone activity. 7. Juvenile activity of the farnesane-type compounds on Locusta migratoria L and Schistocerca gregaria (Forsk). PubMed: Natural and synthetic materials with insect hormones activity. 8. Juvenile activity of the farnesane-type compounds on Galleria mellonella.