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Sigma-Aldrich

(−)-Terpinen-4-ol

≥95.0% (sum of enantiomers, GC)

Synonym(s):

(R)-1-Isopropyl-4-methyl-3-cyclohexen-1-ol, (R)-p-Menth-1-en-4-ol

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About This Item

Empirical Formula (Hill Notation):
C10H18O
CAS Number:
20126-76-5
Molecular Weight:
154.25
MDL number:
MFCD00167108
UNSPSC Code:
12352002
PubChem Substance ID:
57646932
NACRES:
NA.22

Quality Level

100

assay

≥95.0% (sum of enantiomers, GC)

optical activity

[α]20/D -25±6°, neat

optical purity

enantiomeric ratio: ~2:1

refractive index

n20/D 1.479

density

0.934 g/mL at 20 °C

SMILES string

CC(C)[C@@]1(O)CCC(C)=CC1

InChI

1S/C10H18O/c1-8(2)10(11)6-4-9(3)5-7-10/h4,8,11H,5-7H2,1-3H3/t10-/m0/s1

InChI key

WRYLYDPHFGVWKC-JTQLQIEISA-N

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General description

Terpinen-4-ol, a monoterpenoid alcohol, is the key constituent of tea tree (Melaleuca alternifolia) oil.

Application

(-)-Terpinen-4-ol has been used as a standard for the determination of the composition of Lavandula stoechas essential oil by fast gas chromatography-electronic impact ionization/mass spectrometry (FGC-EI/MS).

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

10 - Combustible liquids

wgk_germany

WGK 3

flash_point_f

174.2 °F - closed cup

flash_point_c

79 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Evaluation of the anticonvulsant activity of terpinen-4-ol
Sousa, Dami?o P. de, et al
Zeitschrift fur Naturforschung C, 64(1-2), 1-5 (2009)
Laura de Fátima Souto Maior et al.
Clinical oral investigations, 23(7), 2837-2848 (2019-05-22)
This study investigated the anti-Candida activity and the Shore A hardness of a tissue conditioner (Softone™) modified by incorporation of terpinen-4-ol and cinnamaldehyde. Agar diffusion, microdilution, and mechanism of action methods were performed to determine to evaluate the antifungal activity
Zhenbiao Li et al.
Applied microbiology and biotechnology, 104(5), 2163-2178 (2020-01-26)
Tea tree oil (TTO) and its two characteristic components (terpinen-4-ol and 1,8-cineole) have been shown to inhibit Botrytis cinerea growth. In this study, we conducted a transcriptome analysis to determine the effects of TTO and its characteristic components, alone and
Lavandula stoechas essential oil from Spain: Aromatic profile determined by gas chromatography-mass spectrometry, antioxidant and lipoxygenase inhibitory bioactivities.
Carrasco A, et al.
Industrial Crops and Products, 73, 16-27 (2015)
P H Hart et al.
Inflammation research : official journal of the European Histamine Research Society ... [et al.], 49(11), 619-626 (2000-12-29)
To evaluate potential antiinflammatory properties of tea tree oil, the essential oil steam distilled from the Australian native plant, Melaleuca alternifolia. The ability of tea tree oil to reduce the production in vitro of tumour necrosis factor-alpha (TNFalpha), interleukin (IL)-1beta
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