Field trapping of three Epinotia species with (Z,Z)-7,9-dodecadienyl acetate (Lepidoptera: Tortricidae) was written by Reed, D. W.;Chisholm, M. D.. And the article was included in Journal of Chemical Ecology in 1985.Safety of (E)-Dodeca-9,11-dien-1-yl acetate The following contents are mentioned in the article:
A field survey of the geometrical isomers of 7,9-dodecadienyl alc., acetate, and aldehyde has resulted in attractants and inhibitors for 3 species of tortricid moths. Epinotia silvertoniensis And an undescribed Epinotia species were all attracted to (Z,Z)-7,9-dodecadienyl acetate. Another Epinotia species was attracted to (Z,Z)-7,9-dodecadienyl acetate and (Z,Z)-7,9-dodecadien-1-ol. Electroantennogram data and inhibition patterns for one of the Epinotia species were also reported. In addition, E. criddleana was attracted to lures containing (E)-9-dodecenyl acetate. This study involved multiple reactions and reactants, such as (E)-Dodeca-9,11-dien-1-yl acetate (cas: 50767-78-7Safety of (E)-Dodeca-9,11-dien-1-yl acetate).
(E)-Dodeca-9,11-dien-1-yl acetate (cas: 50767-78-7) belongs to esters. Esters are widespread in nature and are widely used in industry. In nature, fats are in general triesters derived from glycerol and fatty acids. Esters are responsible for the aroma of many fruits. Esterification is the general name for a chemical reaction in which two reactants (typically an alcohol and an acid) form an ester as the reaction product. Esters are common in organic chemistry and biological materials.Safety of (E)-Dodeca-9,11-dien-1-yl acetate
Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics