Names | |
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IUPAC name
(1,3-Dioxo-4,5,6,7-tetrahydroisoindol-2-yl)methyl 2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropane-1-carboxylate
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Preferred IUPAC name
(1,3-Dioxo-1,3,4,5,6,7-hexahydro-2H-isoindol-2-yl)methyl 2,2-dimethyl-3-(2-methylprop-1-en-1-yl)cyclopropane-1-carboxylate | |
Identifiers | |
3D model (JSmol)
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ChEBI | |
ChemSpider | |
ECHA InfoCard | 100.028.829 |
EC Number |
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KEGG | |
PubChem CID
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RTECS number |
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UNII | |
CompTox Dashboard (EPA)
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Properties | |
C19H25NO4 | |
Molar mass | 331.406 g/mol |
Appearance | white crystalline solid |
Odor | strong, pyrethrum-like |
Density | 1.108 g/cm3 |
Melting point | 65 to 80 °C (149 to 176 °F; 338 to 353 K) |
0.00183 g/100 mL | |
Solubility | soluble in methane, hexane slightly soluble in acetone, n-octanol, ethanol very slightly soluble in xylene |
log P | 4.73 |
Vapor pressure | 10 Pa |
Refractive index (nD)
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1.5175 |
Pharmacology | |
P03BA04 (WHO) QP53AC13 (WHO) | |
Hazards | |
Lethal dose or concentration (LD, LC): | |
LD50 (median dose)
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20,000 mg/kg (rat, oral) |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Tetramethrin is a potent synthetic insecticide in the pyrethroid family. It is a white crystalline solid with a melting point of 65–80 °C. The commercial product is a mixture of stereoisomers.
It is commonly used as an insecticide, and affects the insect's nervous system. It is found in many household insecticide products.[1]
Tetramethrin has an expected half-life of 12.5–14 days in soil and 13–25 days in water.[2] Tetramethrin was classified as a Category 2 carcinogen in 2018 by Directorate-General for the Environment of the European Commission.[3]