Fungicides, Agriculture & Feed, R&D, Biopesticides, Flavor & Fragrance Industry, Pharmaceutical
R&D on Terpinen-4-ol
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Fungicides, Agriculture & Feed, R&D, Biopesticides, Flavor & Fragrance Industry, Pharmaceutical
Terpinen-4-ol is naturally found in various plant essential oils(table 1), ecologically safe with pleasant odor, and has a variety of biological activities.
Familia | Genus | Species | Part | Content of terpinen-4-ol in its essential oil (mg/g) |
Cupressaceae | Sabina | S.vulgaris A | Fruit | 223.0 |
Juniperus | J.indica Bertol | Leaf | 37.0-130.0 | |
Annonaceae | Xylopia | X.aethiopica | Fruit | 129.0 |
Labiatae | Origanum | O.majorana | All parts | 323.0 |
O.ramonense Danin | leaf | 168.0 | ||
O.sbusp.viride | All parts | 168.2 | ||
Nepeta | N.asterotrichus | All parts | 228.0 | |
Stachys | S.gluinosa | All parts | 131.0 | |
Ocimum | O.americanum | All parts | 176.0 | |
Elsholtzia | E.fruiticosa | All parts | 126.0 | |
Compositae | Tanacetum | T.longifolium | Root | 258.0 |
Anthemis | A.carpatica | All parts | 97.0 | |
Rutaceae | Citrus | C.hystriz | Fruit | 175.5 |
Magnoliaceae | Iuicium | I.griffithii | Fruit | 110.0 |
Myrtaceae | Pimenta | P.racemosa | Fruit | 207.2 |
Burseraceae | Dacryodes | D.edulis | Bark | 256.0 |
Pandanceae | Panadanus | P.fascicularis | 152.0 | |
Zingiberaceae | Zingiber | Z.cassumunar Roxb | Leaf, Rootstalk | 505.0 |
Andcardiaceae | Pistacia | P.integerrima | Bark | 303.0 |
Acanthaceae | Strobilanthe | S.callosis | 190.0-230.0 |
Terpinen-4-ol, CAS: 562-74-3, formula C10H18O, has two optical isomers: D-Terpinen-4-ol and L-Terpinen-4-ol. It is pale yellow transparent liquid with unique pleasant odor, volatile and soluble in ether, acetone and other solvents with medium polarity. It can also be synthesized from Terpinolene 4, 8-epoxide or 1,4-Cineole.
Terpinen-4-ol itself or with the combined effect of other ingredients has a variety of biological activities, such as attracting activity, repellent activity, fumigant toxicity and growth inhibitory activity to insects, as well as antimicrobial activity, which bring broad prospects for its development and application in pesticides.
The capture rate of Rhizophagus Grandis Gyll is increased to 21.6% by the attractant composed of equal amount of Terpinen-4-ol, fenchol, borneol, α-terpineol, verbenol, fenchone, camphor and pentane, higher than the rate attracted by its favorite foods. The male and female of Hylotrupes bajulus all show strong tropism to terpinen-4-ol.
With unique odor, terpinen-4-ol has repellent activity for some insects.
It was found that terpinen-4-ol has high insecticidal activity to Tetranychus urticae Koch and other two types of the main pests, and the essential oil which contains terpinen-4-ol has high Fumigant toxicity to Rhyzopertha dominea. As well as many other oxygenated monoterpenes, terpinen-4-ol can also obstacle the development of insects and acari larvae.
Many essential oils containing abundant terpinen-4-ol, shows antimicrobial activity to yeast, lactobacillus, staphylococcus aureus, escheri chia cali, proteus miabilis, klebsirlla pneumaniae, pseudomonas aeruginosa, candida albicans and etc. Two essential oils containing terpinen-4-ol can lower 73.0%~75.8% the ratio of rot fruit as one research said.
As a natural material with abundant sources, aside from its insecticidal and antimicrobial effects, terpinen-4-ol is also widely used in daily chemicals, pharmaceuticals, foods and etc.