Name | lauric acid oleyl ester |
Synonyms | OLEYL LAURATE Einecs 242-842-3 Oleyl dodecanoate lauric acid oleyl ester LAURIC ACID OLEOYL ESTER (Z)-octadec-9-enyl laurate ethyl 4-(5-formylfuran-2-yl)benzoate Dodecanoic acid (Z)-9-octadecenyl ester Dodecanoic acid, (9Z)-9-octadecenyl ester |
CAS | 19149-85-0 |
EINECS | 242-842-3 |
InChI | InChI=1/C14H12O4/c1-2-17-14(16)11-5-3-10(4-6-11)13-8-7-12(9-15)18-13/h3-9H,2H2,1H3 |
Molecular Formula | C30H58O2 |
Molar Mass | 450.78 |
Density | 1.199g/cm3 |
Boling Point | 404.7°C at 760 mmHg |
Flash Point | 198.6°C |
Vapor Presure | 9.24E-07mmHg at 25°C |
Storage Condition | -20°C |
Refractive Index | 1.564 |
use | lauric acid oleyl ester can be used as a reactive diluent for bisphenol a epoxy resin. Small toxicity, easy to use. And can improve the properties of some resins after hardening, such as impact strength. Lauric acid oleyl ester can be used as the active diluent of bisphenol A epoxy resin, which is less toxic, easy to use, and can improve the performance of the resin after hardening. Reference dosage is 5% ~ 15%. |
Synthesis | n-butanol first undergoes a complexation reaction with the ether in the boron trifluoride ether complex to form a positive and negative ion pair. The positive and negative ion pair lies in the etherification reaction of epichlorohydrin to form an etherification intermediate. The etherification intermediate dehydrates chlorine atoms under the action of alkali metal oxides and undergoes a closed-loop reaction to generate n-butyl glycidyl ether (lauric acid oleyl ester): |