(-)-α-Terpineol - CAS 10482-56-1
Category:
Main Product
Product Name:
(-)-α-Terpineol
Catalog Number:
10482-56-1
Synonyms:
(l)-alpha-terpineol; (s)-(-)-p-menth-1-en-8-o; .alpha.,.alpha.-4-trimethyl-,(S)-3-Cyclohexene-1-methanol; 2-(4-Methyl-3-cyclohexen-1-yl)-2-propanol; 3-Cyclohexene-1-methanol, alpha,alpha,4-trimethyl-, (S)-; 3-Cyclohexene-1-methanol,.alpha.,.alpha.-4-trimethyl
CAS Number:
10482-56-1
Molecular Weight:
154.25
Molecular Formula:
C10H18O
Quantity:
Data not available, please inquire.
COA:
Inquire
MSDS:
Inquire
Canonical SMILES:
CC1=CCC(CC1)C(C)(C)O
InChI:
InChI=1S/C10H18O/c1-8-4-6-9(7-5-8)10(2,3)11/h4,9,11H,5-7H2,1-3H3/t9-/m1/s1
InChIKey:
WUOACPNHFRMFPN-SECBINFHSA-N
Chemical Structure
CAS 10482-56-1 (-)-α-Terpineol

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Reference Reading


1.Fumigant Toxicity of Lamiaceae Plant Essential Oils and Blends of Their Constituents against Adult Rice Weevil Sitophilus oryzae.
Kim SW1, Lee HR2, Jang MJ3, Jung CS4, Park IK5,6. Molecules. 2016 Mar 16;21(3). pii: E361. doi: 10.3390/molecules21030361.
To find a new and safe alternative to conventional insecticides, we evaluated the fumigant toxicity of eight Lamiaceae essential oils and their constituents against the adult rice weevil Sitophilus oryzae. Of the eight species tested, hyssop (Hyssopus offcinalis), majoram (Origanum majorana), and Thymus zygis essential oils showed strong fumigant toxicity against S. oryzae adults at 25 mg/L air concentration. Constituents of active essential oils were analyzed by gas chromatography coupled to flame ionization detector (FID) and gas chromatography-mass spectrometry. A total of 13, 15, and 17 compounds were identified from hyssop, majoram, and Thymus zygis essential oils, respectively. Pinocamphone and isopinocamphone were isolated by open column chromatography. Among the test compounds, pinocamphone and isopinocamphone showed the strongest fumigant toxicity against S. oryzae. Sabinene hydrate, linalool, α-terpineol, and terpinen-4-ol exhibited 100% fumigant toxicity against S.
2.DoOR 2.0 - Comprehensive Mapping of Drosophila melanogaster Odorant Responses.
Münch D1, Galizia CG1. Sci Rep. 2016 Feb 25;6:21841. doi: 10.1038/srep21841.
Odors elicit complex patterns of activated olfactory sensory neurons. Knowing the complete olfactome, i.e. the responses in all sensory neurons for all relevant odorants, is desirable to understand olfactory coding. The DoOR project combines all available Drosophila odorant response data into a single consensus response matrix. Since its first release many studies were published: receptors were deorphanized and several response profiles were expanded. In this study, we add unpublished data to the odor-response profiles for four odorant receptors (Or10a, Or42b, Or47b, Or56a). We deorphanize Or69a, showing a broad response spectrum with the best ligands including 3-hydroxyhexanoate, alpha-terpineol, 3-octanol and linalool. We include all of these datasets into DoOR, provide a comprehensive update of both code and data, and new tools for data analyses and visualizations. The DoOR project has a web interface for quick queries (http://neuro.uni.
3.α-Terpineol attenuates morphine-induced physical dependence and tolerance in mice: role of nitric oxide.
Parvardeh S1, Moghimi M1, Eslami P2, Masoudi A1. Iran J Basic Med Sci. 2016 Feb;19(2):201-8.
OBJECTIVES: Dependence and tolerance to opioid analgesics are major problems limiting their clinical application. α-Terpineol is a monoterpenoid alcohol with neuroprotective effects which is found in several medicinal plants such as Myrtus communis, Laurus nobilis, and Stachys byzantina. It has been shown that some of these medicinal plants such as S. byzantina attenuate dependence and tolerance to morphine. Since α-terpineol is one of the bioactive phytochemical constituent of these medicinal plants, the present study was conducted to investigate the effects of α-terpineol on morphine-induced dependence and tolerance in mice.
4.Acaricidal activity of Asarum heterotropoides root-derived compounds and hydrodistillate constitutes toward Dermanyssus gallinae (Mesostigmata: Dermanyssidae).
Kim JR1, Perumalsamy H2, Lee JH3, Ahn YJ2, Lee YS4, Lee SG3. Exp Appl Acarol. 2016 Apr;68(4):485-95. doi: 10.1007/s10493-015-0005-2. Epub 2015 Dec 26.
The acaricidal activity of Asarum heterotropoides root-derived principles, methyleugenol, safrole, 3-carene, α-asarone, pentadecane and A. heterotropoides root steam distillate constituents was tested against poultry red mites Dermanyssus gallinae (De Geer). All active principles were identified by spectroscopic analysis. Results were compared with those of two conventional acaricides, benzyl benzoate and N,N-diethyl-3-methylbenzamide (DEET). Methyleugenol (24 h LC50 = 0.57 µg/cm(2)) and safrole (24 h LC50 = 8.54 µg/cm(2)) were the most toxic compounds toward D. gallinae, followed by 3,4,5-trimethoxytoluene, 3,5-dimethoxytoluene, estragole, α-terpineol, verbenone, eucarvone, linalool, and terpinen-4-ol (LC50 = 15.65-27.88 µg/cm(2)). Methyleugenol was 16.7× and 11.0× more toxic than benzyl benzoate (LC50 = 9.52 μg/cm(2)) and DEET (LC50 = 6.28 μg/cm(2)), respectively; safrole was 1.1× and 0.73× more toxic. Asarum heterotropoides root-derived materials, particularly methyleugenol and safrole, merit further study as potential acaricides.