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General Material Information

Preferred name (-)-cubenol
Trivial Name (1S,4R,4aR,8aR)-4,7-dimethyl-1-propan-2-yl-2,3,4,5,6,8a-hexahydro-1H-naphthalen-4a-ol
Short Description (1S,4R,4aR,8aR)-4,7-dimethyl-1-(propan-2-yl)-1,3,4,5,6,8a-hexahydronaphthalen-4a(2H)-ol
Formula C15 H26 O
CAS Number 21284-22-0
Deleted CAS Number 19912-64-2
FDA UNII Search
Nikkaji Number J15.759G
xLogP3-AA 3.70 (est)
NMR Predictor External link
Synonyms
  • 10bH- cadin-4-en-1-ol
  • (1S,4R,4aR,8aR)-4,7-dimethyl-1-(propan-2-yl)-1,3,4,5,6,8a-hexahydronaphthalen-4a(2H)-ol
  • (1S,4R,4aR,8aR)-4,7-dimethyl-1-propan-2-yl-2,3,4,5,6,8a-hexahydro-1H-naphthalen-4a-ol
  • (1S- (1alpha,4beta, 4abeta,8aalpha))- 1,3,4,5,6,8a- hexahydro-4,7-dimethyl-1-(1-methyl ethyl)-4a(2H)-naphthalenol
  • (1S,4R,4aR,8aR)-1-iso propyl-4,7-dimethyl-1,3,4,5,6,8a-hexahydronaphthalen-4a(2H)-ol

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Literature & References

(1S,4R,4aR,8aR)-4,7-dimethyl-1-propan-2-yl-2,3,4,5,6,8a-hexahydro-1H-naphthalen-4a-ol
NIST Chemistry WebBook:Search Inchi
Pubchem (cid):11770062
Pubchem (sid):135349547
Flavornet:21284-22-0
Pherobase:View
Publications by PubMed
Aroma changes of black tea prepared from methyl jasmonate treated tea plants.
Essential oil characterization of two Azorean Cryptomeria japonica populations and their biological evaluations.
[(2)H26]-1-epi-Cubenol, a completely deuterated natural product from Streptomyces griseus.
Chemical composition and biological activities of the essential oil from Calamintha nepeta plants from the wild in southern Italy.
Essential oil composition of Ficus benjamina (Moraceae) and Irvingia barteri (Irvingiaceae).
Chemical composition, antimicrobial and antioxidant properties of the volatile oil and methanol extract of Xenophyllum poposum.
Chemical composition of essential oil of Ferulago macrocarpa (Fenzl) Boiss. fruits.
Composition of the essential oil of Buddleja thyrsoides Lam. leaves from Brazil.
In vitro antimicrobial properties and chemical composition of Santolina chamaecyparissus essential oil from Algeria.
Evaluation of volatile constituents of Cochlospermum angolense.
Antifungal properties of Japanese cedar essential oil from waste wood chips made from used sake barrels.
Chemical composition and antioxidant activity of the essential oil of Tabernaemontana catharinensis A. DC. leaves.
Composition of three essential oils, and their mammalian cell toxicity and antimycobacterial activity against drug resistant-tuberculosis and nontuberculous mycobacteria strains.
Chemical and biological evaluation of essential oils from two species of Myrtaceae - Eugenia uniflora L. and Plinia trunciflora (O. Berg) Kausel.
Variation in the volatile constituents of Artemisia annua var. CIM-Arogya during plant ontogeny.
Free Radical Scavenging Potential and Essential Oil Composition of the Dorema glabrum Fisch. C.A. Mey Roots from Iran.
Biological activity of the essential oil of Kadsura longipedunculata (Schisandraceae) and its major components.
Antimicrobial activity and chemical composition of endemic Centaurea cariensis subsp. niveo-tomentosa.
A new epoxy-cadinane sesquiterpene from the marine brown alga Dictyopteris divaricata.
Identification of a novel compound that inhibits iNOS and COX-2 expression in LPS-stimulated macrophages from Schisandra chinensis.
Comparison of antioxidant and free radical scavenging activities of the essential oils from flowers and fruits of Otostegia persica Boiss.
Insecticidal activity of Valeriana jatamansi (Valerianaceae) against mosquitoes.
The essential oil qualitative and quantitative composition in the needles of Pinus sylvestris L. growing along industrial transects.
Volatile oil from Guarea macrophylla ssp. tuberculata: seasonal variation and electroantennographic detection by Hypsipyla grandella.
Screening of chemical composition and antifungal and antioxidant activities of the essential oils from three Turkish artemisia species.
[Contrastive analysis of volatile oil from Serissa serissoides in different seasons].
Aroma compound analysis of Piper nigrum and Piper guineense essential oils from Cameroon using solid-phase microextraction-gas chromatography, solid-phase microextraction-gas chromatography-mass spectrometry and olfactometry.
Cytotoxic butanolides and secobutanolides from the stem wood of Formosan Lindera communis.
Five new cadinane-type sesquiterpenes from the heartwood of Chamaecyparis obtusa var. formosana.
Volatile secondary metabolite pattern of callus cultures of Chamomilla recutita.

Other Information

PhysChem Properties

Material listed in food chemical codex No
Molecular weight 222.37141418457
Boiling Point 300 to 302°C @ 760 mm Hg
Flash Point TCC Value 128.33 °C TCC
logP (o/w) 4.97
Solubility
alcohol Yes
water, 9.13 mg/L @ 25 °C (est) Yes

Organoleptic Properties

Odor Type: Spicy
spicy, herbal, tea green tea
General comment At 100.00 %. spicy herbal green tea
Flavor Type: Spicy
spicy
General comment Spicy

Occurrences

Safety Information

Safety information

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

Safety in use information

Category:
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
Recommendation for (-)-cubenol usage levels up to:
2.0000 % in the fragrance concentrate.

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 :11770062
National Institute of Allergy and Infectious Diseases:Data
(1S,4R,4aR,8aR)-4,7-dimethyl-1-propan-2-yl-2,3,4,5,6,8a-hexahydro-1H-naphthalen-4a-ol
Chemidplus:021284220