aristolene

(-)-9-aristolene

CAS: 6831-16-9 C15 H24 MW: 204.35628000

Identification

Namearistolene
IUPACaristol-9-ene
CAS Number6831-16-9
FDA UNIISearch
Molecular FormulaC15 H24
Molecular Weight204.35628000
MDL NumberMFCD00042955

Regulatory

Physical Properties

Assay 95.00 to 100.00
Food Chemicals Codex Listed No
Boiling Point 259.90 °C. @ 760.00 mm Hg (est)
Vapor Pressure 0.020000 mmHg @ 25.00 °C. (est)
Flash Point 211.00 °F. TCC ( 99.30 °C. ) (est)
logP (o/w) 6.336 (est)
Soluble in water, 0.07675 mg/L @ 25 °C (est)

No sensory data available

Safety Information

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

Categorynatural substances and extractives
Recommendation for aristolene usage levels up tonot for fragrance use.
Recommendation for aristolene flavor usage levels up tonot for flavor use.

No supplier data available

Potential Uses

None Found

Natural Occurrence

asarum canadense root oil @ 0.20% Data

Synonyms

aristol-9-ene (-)-9- aristolene PubMed: Effect of gibberellic acid (GA), indole acetic acid (IAA) and benzylaminopurine (BAP) on the synthesis of essential oils and the isomerization of methyl chavicol and trans-anethole in Ocimum gratissimum L. PubMed: Volatile organic compounds of six French Dryopteris species: natural odorous and bioactive resources. PubMed: Increases of 2-furanmethanol and maltol in Korean red ginseng during explosive puffing process. PubMed: Comparative study on volatile components of Nardostachys rhizome. PubMed: Biotransformation of aristolane- and 2,3-secoaromadendrane-type sesquiterpenoids having a 1,1-dimethylcyclopropane ring by Chlorella fusca var. vacuolata, mucor species, and Aspergillus niger. PubMed: Gansongon, a New Aristolane Ketone from Nardostachys chinesis Batalin and Structure Revision of an Aristolenol. PubMed: Insecticidal activity of Valeriana jatamansi (Valerianaceae) against mosquitoes. PubMed: Analytical discrimination of poisonous and nonpoisonous chemotypes of giant fennel (Ferula communis L.) through their biologically active and volatile fractions. PubMed: Terpenoids from the roots and rhizomes of Nardostachys chinensis.