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  • Coumachlor is used as a rodenticide. The chemical may be absorbed through the skin. Ingestion and other exposures to the chemical can cause various symptoms
  • The Chemical formula for  Coumachlor  is  C19H15ClO4
  • The enantiomers of the rodenticide coumachlor were separated by reversed phase HPLC using a Chirobiotic V column and detected by UV at 254nm.
  • Racemic mixtures of five acidic drugs have been successfully separated by supercritical fluid chromatography (SFC) using macrocyclic antibiotic chiral stationary phases (CSPs).
  • Using HPLCMS-MS both enantiomers of WAR and coumachlor (COU) were reproducibly separated in 8 min on a β-cyclodextrin column with limit of detection as low as 1ng/mL.
  • The anticoagulant rodenticides were greatly effective against the albino mouse Mus musculus var. albus, since they could cause a final mortality of hundred percent in a mean time ranging merely between 7 & 9 days. Chlorophacinone was more potent and effective than coumachlor; at its lowered concentrations of 25 and 44.5 ppm was more acceptable than coumachlor.
  • The advent of a highly potent but slow-acting rodenticide molecule, brodifacoum, has allowed the development of the pulsed baiting technique. This practical technique is highly effective and offers very significant savings both in bait and labour compared to first-generation anticoagulants, with excellent levels of control.
  • Four rodent control techniques-sustained baiting (SB) with cournachlor. pulsed baiting (PB) with brodifacoum. a lethal electrified barrier (LEB), and a nonlethal electrified barrier (NLEB)-were evaluated on the experimental fann of the International Rice Research Institute (IRRI) in the Philippines.
General Information
  • Coumachlor - Chemical Information
  • Coumachlor - Data Sheet
  • Coumachlor


  • Consultant from Africa
  • Consultant from USA


  • Chiral analyses using molecular micelles and multiple regression modeling in chromatographic and spectroscopic methods
  • A comparison of ionic liquids to molecular organic solvents as additives for chiral separations in
    micellar electrokinetic chromatography
  • The Comparative rodenticidal efficiency of five anti-coagulants
  • Separation and Determination of Warfarin Enantiomers in Human Plasma Using a Novel Polymeric Surfactant for Micellar Electrokinetic Chromatography-Mass Spectrometry


  • Anticoagulant Rodenticide Intoxication in Animals - A Review
  • A review of anticoagulant rodenticides in current use
  • Synthesis, antifeedant and insect growth-regulating activity of N-(2-nitro) benzylidene-3 aminocoumarin complexes and their physio-chemical characterization
  • Confirmation of indandione rodenticide toxicoses by mass spectrometry/mass spectrometry
  • A comparison of four rodent control methods in Philippine experimental rice felds
  • Screening for Drugs and Toxic Compounds in Human Serum
  • Pulsed Baiting - A new technique for high potency, slow acting rodenticides
  • Plant from Canada
  • Plant from Delhi


  • Assessing some Potential Environmental Impacts from Agricultural Anticoagulant Uses
  • Integrated Pest Management Collaborative Research Support Program (IPM CRSP) Eastern Africa Program


  • Rodenticidal composition
  • Rodenticide compositions comprising an artificial sweetener and a rodenticide
  • Rodenticide Mixture
  • Aqueous Rodenticide Formulations
  • Rodenticide for toxic wick

Material Safety Data Sheet

  • Coumachlor - Aldrich
  • Coumachlor - Fluka


  • Poisoning of wildlife with anticoagulant in new york
  • Rodenticide poisoning in pets
  • Poisoning caused by pesticides
  • Study of the cytogenetic effects of occupational exposure to pesticides on sanitation workers in Belo Horizonte, Brazil
  • Coumachlor - Human Toxicity


  • The dangerous chemical control act
  • Chemical groups and modes of action of pesticides
  • Pest control report
  • Poisons act


  • Coumachlor suppliers list
  • Supplier from China

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