Permethrin

Assemble a molecular structure model of Permethrin from Authentic Molymod Model Parts by Indigo.

Permethrin is classed as a synthetic neurotoxic pyrethroid insecticide that targets a wide variety of insects. It is a synthetic chemical compound based on extracts from the chrysanthemum flower. Permethrin control mechanism of arthropods such as insects & ticks is depolarization of sodium transport channels in neuronal membranes to cause paralysis.

Permethrin's chemical structure is a cyclopropanecarboxylate ester based on a cyclopropane ring. It has four stereoisomers with the (1R,3S)-trans and (1R,3R)-cis enantiomers responsible for the insecticidal properties of permethrin.

Common Uses for Permethrin:

  1. Food and Feed Crops
  2. Mosquito Control
  3. Lawns and Gardens
  4. Livestock and Pets
  5. Medications - Scabies and head lice
  6. Spraying buildings, clothing
  7. Flea Collars
  8. Restaurants
  9. Tick Repellant

A molecular model of Permethrin in the Molymod Hybrid Dome style uses the atoms & bonds in the parts list below. Our free 3D Molecular Model Builder shows other styles & allows for image rotation as an assembly guide.

Chemical data
Molecular Weight Chemical Formula
391.2932 C21H20Cl2O3

Permethrin molecular model built with Molymod Atoms & Bonds

Hybrid Dome
Open Sphere
Orbit Basic
Orbit Flexible
Parts
Synonyms
IUPAC Name: (3-phenoxyphenyl)methyl 3-(2,2-dichloroethenyl)-2,2-dimethylcyclopropane-1-carboxylate , InChI: 1S/C21H20Cl2O3/c1-21(2)17(12-18(22)23)19(21)20(24)25-13-14-7-6-10-16(11-14)26-15-8-4-3-5-9-15/h3-12,17,19H,13H2,1-2H3 , InChIKey: RLLPVAHGXHCWKJ-UHFFFAOYSA-N , SMILES: CC1(C(C1C(=O)OCC2=CC(=CC=C2)OC3=CC=CC=C3)C=C(Cl)Cl)C , CAS: 52645-53-1 , Lyclear, Nix, Pounce, Ambush,Torpedo, Cellutec, Ectiban, Pramiex, Exmin, Indothrin