Flocoumafen
![Flocoumafen Structure](CAS/GIF/90035-08-8.gif)
- CAS No.
- 90035-08-8
- Chemical Name:
- Flocoumafen
- Synonyms
- STORM;stratgem;wl108366;Stratagen;Storm(TM);FLOCUMAFEN;FLOCOUMAFEN;flocoumafene;aphthyl)coumarin;Storm(rodenticide)
- CBNumber:
- CB6671271
- Molecular Formula:
- C33H25F3O4
- Molecular Weight:
- 542.54
- MOL File:
- 90035-08-8.mol
- Modify Date:
- 2024/7/2 8:55:14
Melting point | 181 °C |
---|---|
Boiling point | 672.4±55.0 °C(Predicted) |
Density | 1.2 g/cm3 |
vapor pressure | 1.33 x l0-10 Pa (25 °C) |
Flash point | 23 °C |
solubility | Chloroform (Slightly), Methanol (Slightly) |
form | Solid |
Water Solubility | 1.1 mg l-1 |
pka | 4.50±1.00(Predicted) |
color | White to off-white |
InChIKey | KKBGNYHHEIAGOH-UHFFFAOYSA-N |
EPA Substance Registry System | 2H-1-Benzopyran-2-one, 4-hydroxy-3-[1,2,3,4-tetrahydro-3-[4-[[4-(trifluoromethyl)phenyl]methoxy]phenyl]-1-naphthalenyl]- (90035-08-8) |
SAFETY
Risk and Safety Statements
Symbol(GHS) | ![]() ![]() ![]() GHS06,GHS08,GHS09 |
---|---|
Signal word | Danger |
Hazard statements | H300+H310+H330-H360D-H372-H410 |
Precautionary statements | P202-P260-P273-P280-P302+P352+P310-P304+P340+P310 |
Hazard Codes | T+,N |
Risk Statements | 26/27/28-48/23/24/25-50/53 |
Safety Statements | 28-36/37/39-45-60-61 |
RIDADR | 3027 |
WGK Germany | 3 |
RTECS | DJ3100300 |
HazardClass | 6.1(a) |
PackingGroup | I |
Toxicity | LD50 in rats, mice, rabbits (mg/kg): 0.25, 0.8, 0.2 orally (Bowler) |
Flocoumafen Chemical Properties,Uses,Production
Uses
Flocoumafen is a second-generation anti-coagulant used as a rodenticide. It has a very high toxicity and is restricted to indoor use and sewers (in the United Kingdom). This restriction is mainly due to the increased risk to non-target species. Studies have shown that rodents resistant to first-generation anti-coagulants can be adequately controlled with flocoumafen. The chemical substance is off-white solid, does not mix well with water (1.1 mg/L), and is sparingly soluble in acetone, ethanol, xylene, and octanol. Flocoumafen is stable to hydrolysis. Because of the acute toxicity of flocoumafen and its intended use as a rodenticide, chronic toxicity studies have not been reported. However, flocoumafen is known to cause adverse health effects and abnormal prothrombin.
Metabolic pathway
Flocoumafen exists as cis and trans isomers (Scheme 1). The tetralin ring adopts its most stable conformation in each case and the two forms have very similar shapes. Both are active rodenticides. The fate of flocoumafen in soils and plants has not been studied in detail because the compound is usually used as a pelleted bait or in a wax block. This limits its dissipation in the environment. Studies in animals and birds have been conducted as part of the assessment of safety and to investigate mode of action. Metabolism is slow in the rat and rapid in Japanese quail but this difference should be interpreted with care because of the 100-fold difference in dose used (see also Overview).
Degradation
Flocoumafen is a stable compound; no detectable degradation occurs at 50 °C at pH 7-9 over 4 weeks.
Flocoumafen Preparation Products And Raw materials
Raw materials
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