| Nombre del producto | (E)-9-Dodecen-1-yl acetate |
| Abreviatura | E9-12Ac |
| Sinónimos | acetate,(e)-9-dodecen-1-o;TRANS-9-DODECENYL ACETATE;9-DODECENYLACETATE;Acetic acid (E)-9-dodecenyl ester;9E-12Ac;(E)-dodec-9-enyl acetate;(9E)-9-Dodecenyl acetate;(E)-9-Dodecen-1-ol acetate |
| N.º CAS | 35148-19-7 |
| Plaga objetivo | Sparganothis pilleriana; Grape berry moth；European grapevine moth |
| Escenario de aplicación | Fruits |
| Fórmula molecular | C14H26O2 |
| Peso molecular | 226.35 |
| Densidad | 0.881±0.06 g/cm3 (20 ºC 760 Torr) |
| Forma | |
| Punto de ebullición | 300.1±21.0℃ (760 Torr) |
| Temperatura de almacenamiento | |
| Pureza | 90%，95%，98% |
| Aplicación | (E)-9-Dodecen-1-yl acetate (abbreviated as E9-12:OAc) is a key trans-isomer component of the sex pheromone in the date palm moth (Ancylis sativa). Studies show that when mixed with its cis-isomer (Z9-12:OAc) at an 8:2 ratio, it forms a highly effective binary pheromone system, demonstrating strong activity in field electroantennogram and moth-trapping tests. This blend disrupts male orientation to females, significantly reducing mating rates. It has been successfully applied in green control methods, such as polyethylene plastic tube lures, offering advantages like zero pollution, protection of natural enemies, and precise monitoring, making it a prominent tool in integrated pest management. |
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