axyridis to D-limonene and terpinolene
with no aphids: Analytical reagent-grade pure D-limonene and terpinolene
were used to test the behavioral responses of H.
However, based on previous studies at the same study site, the rain forest produces at least 12 different monoterpene species, including [beta]-ocimene and terpinolene
, which are highly reactive with respect to ozone (Jardine et al.
With respect to crop levels, only three--isobutyl alcohol, terpinolene
and diethyl succinate (the latter was only detected in HC treatment)--differed between HC and FC in 2011.
On the other hand, the relative mid beta activity significantly decreased and the relative fast alpha activity significantly increased in the right prefrontal region during the inhalation of terpinolene
Other constituents such as [gamma]-Terpinene,Sabinene hydrate, Terpinolene
, Terpinene-4-ol,[alpha]-Copaene [alpha]-Humulene, Germacrene D, [alpha]-Mumolene, [alpha]-Famesene, [gamma]-Cadinene, [delta]-Cadinene, Calacorene, Caryophyllene oxide I, Caryophyllene oxide II and Palmitic acid were present in amount less the 1%.
1 23 Unidentified 1 1063 1558 -- -- 24 Terpinolene
1083 1274 0.
The components observed are: a) tricyclene, (b) (-) -[alpha]-pinene, (+)-[alpha]-pinene racemate, (c) camphene, (d) 1,4-cineole (e), limonene, (f) terpinolene
, and (g) turpineol.
The only compounds present in the two oils were [alpha]- terpinolene
and the D-germacrene, but at different proportions.
As the monocyclic terpene compounds, there are limonene, dipentene (optical isomer of limonene), terpinolene
, [alpha]-pinene, [beta]-pinene, terpinene, and menthadiene, and these have been used as raw materials for epoxy resins and curing agents.
Thus the presence of [alpha]-pinene, [alpha]-terpinene, [gamma]-terpinene, terpinolene
, [beta]-terpineol, a-terpineol (one the major compounds in fruit extract), 4-terpineol, isoborneol, [gamma]-cadinene (the major compound in leaf extract), [alpha]-cadinene, cadina-1, 4-diene and [sigma]-cadinene may contribute to the diuretic and antiseptic action of the leaf and fruit extracts of the Egyptian J.
5% are due to two terpenes, d-limonene and terpinolene
, and one terpene-alcohol, [alpha]-terpineol.
During storage, the content of esters, terpinene-4-ol and terpineol increased, while levels of aldehydes, myrcene and terpinolene