- 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.
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General
Information
- Coumachlor - Chemical
Information
- Coumachlor - Data
Sheet
- Coumachlor
Consultant
- Consultant from
Africa
- Consultant from USA
Process
- 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
Application
- 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
Technology
- 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
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Plant
- Plant from Canada
- Plant from Delhi
Project
- Assessing some Potential
Environmental Impacts from Agricultural Anticoagulant Uses
- Integrated Pest Management
Collaborative Research Support Program (IPM CRSP) Eastern Africa
Program
Patent
- 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
Toxicity
- 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
Report
- The dangerous chemical control act
- Chemical groups and modes of action of
pesticides
- Pest control report
- Poisons act
Suppliers
- Coumachlor suppliers
list
- Supplier from China
Order the CD-ROM
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