Difenacoum
Difenacoum | ||
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IUPAC name 2-Hydroxy-3-[3-(4-phenylphenyl)-1-tetralinyl]-4-chromenone | ||
Other names Diphenacoum | ||
Identifiers | ||
CAS number | 56073-07-5 | |
PubChem | 41735 | |
KEGG | C16807 | |
Jmol-3D images | Image 1 | |
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Properties | ||
Molecular formula | C31H24O3 | |
Molar mass | 444.52 g/mol | |
Density | 1.27 (98.7% w/w) | |
Melting point | 211.0 – 215.0 °C (98.7% wlw) | |
(verify) (what is: / ?) Except where noted otherwise, data are given for materials in their standard state (at 25 °C (77 °F), 100 kPa) | ||
Infobox references | ||
Difenacoum is an anticoagulant of the 4-hydroxycoumarin vitamin K antagonist type. It has anticoagulant effects and is used commercially as a rodenticide.
Uses
Difenacoum is sold as blue-green pellets intended to be ingested by pests such as rats and mice.
Safety and toxicity
Because other species of mammals and birds may prey upon affected rodents, there is a risk of secondary or tertiary exposure.[1] Using radiolabeled isotopes, difenacoum (and/or its metabolites) has been shown to be distributed across many organ tissues upon oral ingestion, with the highest concentrations occurring in the liver and pancreas.[1]
Difenacoum has been shown to be highly toxic to some species of freshwater fish and green algae despite the fact that difenacoum is weakly soluble in aqueous solutions.[1]
References
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