tefluthrin (racemic)
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Names | |
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Preferred IUPAC name
rac-(2,3,5,6-Tetrafluoro-4-methylphenyl)methyl (1R,3R)-2,2-dimethyl-3-[(1Z)-2-chloro-3,3,3-trifluoroprop-1-en-1-yl]cyclopropane-1-carboxylate | |
Other names
Tefluthrine
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Identifiers | |
3D model (JSmol)
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ChEBI | |
ChEMBL | |
ChemSpider | |
ECHA InfoCard | 100.124.968 |
EC Number |
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KEGG | |
PubChem CID
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UNII | |
CompTox Dashboard (EPA)
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Properties[1] | |
C17H14ClF7O2 | |
Molar mass | 418.74 g·mol−1 |
Appearance | colorless solid |
Density | 1.48 g/mL |
Melting point | 44.6 °C |
Boiling point | 156 °C at 1 mmHg |
0.02 mg/L in water
>500 g/L in acetone, hexane, toluene | |
log P | 6.4 |
Hazards[2] | |
GHS labelling: | |
Danger | |
H300, H310, H330, H410 | |
P260, P262, P264, P270, P271, P273, P280, P284, P301+P310, P302+P350, P304+P340, P310, P320, P321, P322, P330, P361, P363, P391, P403+P233, P405, P501 | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Tefluthrin is the ISO common name[3] for an organic compound that is used as a pesticide.[1] It is a pyrethroid, a class of synthetic insecticides that mimic the structure and properties of the naturally occurring insecticide pyrethrin which is present in the flowers of Chrysanthemum cinerariifolium. Pyrethroids such as tefluthrin are often preferred as active ingredients in agricultural insecticides because they are more cost-effective and longer acting than natural pyrethrins.[4] It is effective against soil pests because it can move as a vapour without irreversibly binding to soil particles: in this respect it differs from most other pyrethroids.[5]