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Details

Stereochemistry ACHIRAL
Molecular Formula C10H18O
Molecular Weight 154.2493
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of .GAMMA.-TERPINEOL

SMILES

CC(C)=C1CCC(C)(O)CC1

InChI

InChIKey=NNRLDGQZIVUQTE-UHFFFAOYSA-N
InChI=1S/C10H18O/c1-8(2)9-4-6-10(3,11)7-5-9/h11H,4-7H2,1-3H3

HIDE SMILES / InChI

Description
Curator's Comment: description was created based on several sources, including: https://www.ncbi.nlm.nih.gov/pubmed/24716612 https://www.ncbi.nlm.nih.gov/pubmed/24250481 https://www.ncbi.nlm.nih.gov/pubmed/15713037 https://www.ncbi.nlm.nih.gov/pubmed/12670156

Terpineol is usually a mixture of three isomers: alpha-, beta-, and gamma-terpineol. gamma-Terpineol is isolated from carrot oils, from the cinnamon tree (Cinnamomum zeylanicum) and Scotch pine (Pinus sylvestris), it is found in Thymus persicus, Wild Rhododendron tomentosum Harmaja and Teucrium persicum Boiss essential oils, as an odorant in Moroccan green olives.

Approval Year

Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
Unknown

Approved Use

Unknown
PubMed

PubMed

TitleDatePubMed
Screening for key odorants in Moroccan green olives by gas chromatography-olfactometry/aroma extract dilution analysis.
2005 Feb 23
Comparative Chemical Composition and Antioxidant Properties of the Essential Oils and Aromatic Water from Teucrium persicum Boiss.
2012 Spring
γ-terpineol inhibits cell growth and induces apoptosis in human liver cancer BEL-7402 cells in vitro.
2014
Chemical Components of Four Essential Oils in Aromatherapy Recipe.
2015 Jun
Antinociceptive activity of the essential oil from Artemisia ludoviciana.
2016 Feb 17
Patents

Patents

Sample Use Guides

In Vivo Use Guide
Unknown
Route of Administration: Unknown
BEL-7402 cells were treated with various concentrations (40, 80, 160, 320 and 640 μg/ml) of γ-terpineol for 48 h. The γ-terpineol significantly suppressed BEL-7402 cell proliferation in a dose-dependent manner.
Name Type Language
.GAMMA.-TERPINEOL
Common Name English
CYCLOHEXANOL, 1-METHYL-4-(1-METHYLETHYLIDENE)-
Systematic Name English
P-MENTH-4(8)-EN-1-OL
Systematic Name English
GAMMA-TERPINEOL
Common Name English
Code System Code Type Description
NCI_THESAURUS
C80899
Created by admin on Fri Dec 15 15:05:13 GMT 2023 , Edited by admin on Fri Dec 15 15:05:13 GMT 2023
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PUBCHEM
11467
Created by admin on Fri Dec 15 15:05:13 GMT 2023 , Edited by admin on Fri Dec 15 15:05:13 GMT 2023
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EPA CompTox
DTXSID2060416
Created by admin on Fri Dec 15 15:05:13 GMT 2023 , Edited by admin on Fri Dec 15 15:05:13 GMT 2023
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NCI_THESAURUS
C45678
Created by admin on Fri Dec 15 15:05:13 GMT 2023 , Edited by admin on Fri Dec 15 15:05:13 GMT 2023
CONCEPT Industrial Aid
CAS
586-81-2
Created by admin on Fri Dec 15 15:05:13 GMT 2023 , Edited by admin on Fri Dec 15 15:05:13 GMT 2023
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ECHA (EC/EINECS)
209-584-3
Created by admin on Fri Dec 15 15:05:13 GMT 2023 , Edited by admin on Fri Dec 15 15:05:13 GMT 2023
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FDA UNII
5PH9U7XEWS
Created by admin on Fri Dec 15 15:05:13 GMT 2023 , Edited by admin on Fri Dec 15 15:05:13 GMT 2023
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