Rotenone
Rotenone is an odorless, colorless, crystalline isoflavone used as a broad-spectrum insecticide, piscicide, and pesticide. It occurs naturally in the seeds and stems of several plants, such as the jicama vine, and in the roots of several other members of the Fabaceae. It was the first-described member of the family of chemical compounds known as rotenoids.
Names | |
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IUPAC name
(5′′R)-4′,5′-Dimethoxy-5′′-(prop-1-en-2-yl)-4′′,5′′-dihydrofuro[2′′,3′′:7,8]rotenan-4-one | |
Systematic IUPAC name
(2R,6aS,12aS)-8,9-Dimethoxy-2-(prop-1-en-2-yl)-1,2,12,12a-tetrahydro[1]benzopyrano[3,4-b]furo[2,3-h][1]benzopyran-6(6aH)-one | |
Other names
Tubatoxin, Paraderil | |
Identifiers | |
3D model (JSmol) |
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ChEBI | |
ChEMBL | |
ChemSpider | |
ECHA InfoCard | 100.001.365 |
KEGG | |
MeSH | Rotenone |
PubChem CID |
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UNII | |
CompTox Dashboard (EPA) |
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Properties | |
C23H22O6 | |
Molar mass | 394.423 g·mol−1 |
Appearance | Colorless to red crystalline solid |
Odor | odorless |
Density | 1.27 g/cm3 @ 20 °C |
Melting point | 165 to 166 °C (329 to 331 °F; 438 to 439 K) |
Boiling point | 210 to 220 °C (410 to 428 °F; 483 to 493 K) at 0.5 mmHg |
Solubility | Soluble in ether and acetone, slightly soluble in ethanol |
Vapor pressure | <0.00004 mmHg (20°C) |
Hazards | |
Lethal dose or concentration (LD, LC): | |
LD50 (median dose) |
60 mg/kg (oral, rat) 132 mg/kg (oral, rat) 25 mg/kg (oral, rat) 2.8 mg/kg (oral, mouse) |
NIOSH (US health exposure limits): | |
PEL (Permissible) |
TWA 5 mg/m3 |
REL (Recommended) |
TWA 5 mg/m3 |
IDLH (Immediate danger) |
2500 mg/m3 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references |
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