Description
This is a novel chinese a pyrethroid ester insecticide for which little published data is available.
Chemical Properties
Dextro-trans Chloropropargyl Permethrin is light gray-yellow crystal with a melting point of 90℃. It is easily soluble in toluene, acetone, cyclohexane and other organic solvents, insoluble in water and other hydroxyl solvents. It is stable to light and heat, and also stable in neutral and slightly acidic medium, but easy to decompose under alkaline conditions.
Definition
ChEBI: Chloroprallethrin is a carboxylic ester obtained by formal condensation between the carboxy group of (1R,3S)-3-(2,2-dichloroethenyl)-2,2-dimethylcyclopropane-1-carboxylic acid and the hydroxy group of (4S)-4-hydroxy-3-methyl-2-(prop-2-yn-1-yl)cyclopent-2-en-1-one. It has a role as a pyrethroid ester insecticide and an agrochemical. It is an organochlorine compound, an enone, a terminal acetylenic compound, a cyclic ketone and a cyclopropanecarboxylate ester.
Production Methods
Chloroprallethrin is produced through the modular ester-assembly route characteristic of many modern pyrethroid-type insecticides. Commercial manufacturers begin by preparing the acid fragment, a chlorinated, highly substituted cyclopropanecarboxylic acid, using established halogenation and cyclopropanation chemistry common across the pyrethroid class. In parallel, they generate the alcohol fragment, a prallethrin-type allylic alcohol built from terpene-derived intermediates. These two components are then coupled via esterification under controlled conditions to form chloroprallethrin. The crude ester is subsequently purified, stripped of residual solvents, and crystallised or stabilised as an oil, yielding technical grade material suitable for formulation.
Mechanism of action
Pyrethroid insecticides generally work by disrupting sodium channels in insect nerve cells, leading to paralysis and death.
Pesticide Type
Insecticide
