gamma-terpineol

General Material Information

Preferred name	gamma-terpineol
Trivial Name	γ-Terpineol
Short Description	cyclohexanol, 1-methyl-4-(1-methylethylidene)-
Formula	C10 H18 O
CAS Number	586-81-2
ECHA Number	209-584-3
FDA UNII	5PH9U7XEWS
Nikkaji Number	J9.439K
xLogP3-AA	2.10 (est)
NMR Predictor	External link
Synonyms	cyclohexanol, 1-methyl-4-(1-methylethylidene)- p- menth-4(8)-en-1-ol 4(8)-p- menthen-1-ol 4(8)-para- menthen-1-ol 1-methyl-4-(1-methyl ethylidene) cyclohexan-1-ol 1-methyl-4-(1-methyl ethylidene) cyclohexanol 1-methyl-4-(1-methylethylidene)cyclohexan-1-ol 1-methyl-4-(1-methylethylidene)cyclohexanol 1-methyl-4-(propan-2-ylidene)cyclohexanol 1-methyl-4-isopropylidene cyclohexan-1-ol 1-methyl-4-propan-2-ylidenecyclohexan-1-ol 4-iso propylidene-1-methylcyclohexanol .gamma.- terpineol g- terpineol 1-methyl-4-propan-2-ylidenecyclohexan-1-ol p-Menth-4(8)-en-1-ol 1-Methyl-4-(1-methylethylidene)cyclohexanol γ-Terpineol 1-Methyl-4-(propan-2-ylidene)cyclohexan-1-ol

	1-methyl-4-propan-2-ylidenecyclohexan-1-ol
NIST Chemistry WebBook:	Search Inchi
Pubchem (cid):	11467
Pubchem (sid):	134975971
Pherobase:	View

Publications by PubMed
Niaouli oils from different sources: analysis and influence on cutaneous permeation of estradiol in vitro.
Screening for key odorants in Moroccan green olives by gas chromatography-olfactometry/aroma extract dilution analysis.
[Analysis of terpineol and improvement of technology process in terpineol production].
Bacterial susceptibility to and chemical composition of essential oils from Thymus kotschyanus and Thymus persicus.
Chemical Components of Four Essential Oils in Aromatherapy Recipe.
γ-terpineol inhibits cell growth and induces apoptosis in human liver cancer BEL-7402 cells in vitro.
Supplementation of moist and dehydrated citrus pulp in the diets of sheep artificially and naturally infected with gastrointestinal nematodes on the parasitological parameters and performance.
Composition of the essential oil of the Rhododendron tomentosum Harmaja from Estonia.
Comparative Chemical Composition and Antioxidant Properties of the Essential Oils and Aromatic Water from Teucrium persicum Boiss.
Degradation of terpenes and terpenoids from Mediterranean rangelands by mixed rumen bacteria in vitro.
Niaouli oils from different sources: analysis and influence on cutaneous permeation of estradiol in vitro.

(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):	C17518
HMDB (The Human Metabolome Database):	HMDB36993
FooDB:	FDB015965
Typical G.C.
VCF-Online:	VCF Volatile Compounds in Food
ChemSpider:	View
Wikipedia:	View

Material listed in food chemical codex	No
Molecular weight	154.2526550293
Melting Point	68 to 70°C @ 760 mm Hg
Boiling Point	218 to 219°C @ 760 mm Hg
Vapor Pressure	0.027 mmHg @ 25 °C
Flash Point TCC Value	88.33 °C TCC
logP (o/w)	2.613 est
Solubility
alcohol	Yes
water, very slightly	Yes
water, 260.1 mg/L @ 25 °C (est)	Yes
water	No

Applications	natural substances and extractives
Odor purposes	Acacia, Aldehydic, Almond, Amber, Anise, Apple blossom, Apricot, Balsam, Bay rum, Bayberry, Bergamot, Bluebell, Bois de rose, Bouquet, Bubble gum, Cajeput, Cardamom oil replacer, Carnation, Cassia, Cedarwood, Cherry, Christmas, Cinnamon, Citrus, Clary sage oil replacer, Clover, Crabapple blossom, Cubeb, Cypress oil replacer, Dillenia, Elder flower, Eucalyptus oil replacer, Evergreen, Fagonia, Fern, Fig, Fir needle oil replacer, Floral, Frangipani plumeria, Gardenia, Genet, Geranium, Grape, Grapefruit, Green, Green grass, Greenhouse, Hawthorn, Herbal, Hollyberry, Honeysuckle, Hyacinth, Jasmin, Jonesia, Juniper, Juniper berry, Lavandin, Lavender, Leather, Lemon, Lemongrass, Licorice, Lilac, Lily, Lime, Linaloe wood, Linden flower, Lotus, Lovage root, Mace, Magnolia, Muguet, Mulberry, Musk, Narcissus, Neroli, Niaouli, Nutmeg, Orange, Orange blossom, Fresh outdoors, Passion fruit, Peach, Pennyroyal, Peony, Petitgrain, Pine forest, Pineapple, Plum mirabelle plum, Potpourri, Powder, Rain, Raspberry, Rose, Sandalwood, Sassafras, Snake root, Spearmint, Spice, Sweet pea, Thyme oil white replacer, Tuberose, Valerian, Wallflower, Wintergreen, Wisteria, Woody
Flavoring purposes	Cajeput, Cubeb, Linaloe wood, Lovage root, Lychee, Mango, Mimosa, Pennyroyal, Snake root, Tea green tea, Tutti frutti, Valerian
Other purposes	Lux beauty shower soap, Meadow, Strawberry leaf, Tide


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

Category:
natural substances and extractives
Recommendation for gamma-terpineol usage levels up to:
	not for fragrance use.

Recommendation for gamma-terpineol flavor usage levels up to:
	not for flavor use.

AIDS Citations:Search

Cancer Citations:Search

Toxicology Citations:Search

EPA Substance Registry Services (TSCA):586-81-2

EPA Substance Registry Services (SRS):Registry

Laboratory Chemical Safety Summary :11467

National Institute of Allergy and Infectious Diseases:Data

1-methyl-4-propan-2-ylidenecyclohexan-1-ol

Chemidplus:0000586812