coumatetralyl - Coumatetralyl 3alphatetralyl4hydroxycoumarin was introduced by Bayer brogger AG with the trademark name of Racumin It has been used for commensal control in many countries It is formulated as a dry bait 00375 a liquid bait of its sodiumsalt and a 075 tracking dust Chalermchaikit et al 1993Pure coumatetralyl is a colorless powder which is stable at temperatures below 150C COUMATETRALYL is a yellowishwhite powder used as a rodenticide and an anticoagulant It may cause bleeding liver damage and fire hazards Learn about its identification hazards response and regulatory information Coumatetralyl an overview ScienceDirect Topics Coumatetralyl IUPAC name 4hydroxy31 2 3 4tetrahydro1naphthyl coumarin CAS number 5836293 is a rodenticide produced by Bayer Environmental Science at Bayer AG site in Uerdingen Germany Coumatetralyl technical grade produced by Bayer AG is a racemic mixture of R and S enantiomers is also called Racumin S technical ENE 1183b Coumatetralyl Producttype PT 14 Rodenticides ECHA Common Name COUMATETRALYL CAS Number 5836293 DOT Number UN 3027 HAZARD SUMMARY Coumatetralyl can affect you by ingestion and may be absorbed through the skin High or repeated exposure can reduce the ability of the blood to clot causing hemorrhage Symptoms may include easy bruising nosebleeds bleeding gums andor blood in Coumatetralyl C19H16O3 CID 54678504 PubChem 1st generation anticoagulants RRAC Resistance guide Coumatetralyl an overview ScienceDirect Topics PDF Coumatetralyl Hazard Summary Workplace Exposure Limits Ways of Reducing Coumatetralyl is a secondgeneration anticoagulant rodenticide that inhibits vitamin K epoxidase Learn about its chemical structure properties uses and analytical methods for detection in biological samples Particulatephase coumatetralyl will be removed ambre from the atmosphere by wet or dry deposition Coumatetralyl contains chromophores that absorb at wavelengths 290 nm and therefore may be susceptible to direct photolysis by sunlight If released to soil coumatetralyl is expected to have slight mobility based upon an estimated Koc of 3900 COUMATETRALYL CAMEO Chemicals NOAA Coumatetralyl 5836293 ChemicalBook Coumatetralyl is produced by the condensation of 4 hydroxycoumarin with 1234tetrahydro1naphthol 28 First introduced in 1956 coumatetralyl is one of the most widely used firstgeneration anticoagulants It is not however available in the United States Chemical Properties Coumatetralyl is a yellowishwhite crystalline solid Uses Coumatetralyl was launched in 1957 and is marketed worldwide and is more potent than warfarin and some other firstgeneration compounds It is used as a tracking powder or as a cereal bait wax block or paste for rodent control Like other anticoagulant rodenticides coumatetralyl inhibits the formation of vitamin Kdependent clotting factors Coumatetralyl is an anticoagulant of the 4hydroxycoumarin vitamin K antagonist type used as a rodenticide 2 Common applications Coumatetralyl is commonly used with grains and other cereals as a rodent poison in conjunction with a tracking powder to monitor feeding activity in a particular area Tracking powder also clings to fur which Coumatetralyl Wikipedia Coumatetralyl is an anticoagulant of the warfarin type Symptoms of overexposure relate to failure of the blood clotting mechanism and include bleeding gums and failure of blood clotting after skin wounds After one exposure the toxicity of coumatetralyl is relatively low however if overexposure continues for several days the totoh product becomes Coumatetralyl wikidoc
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