Names | |
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Preferred IUPAC name
1,4,5,6,7,8,8-Heptachloro-3a,4,7,7a-tetrahydro-1H-4,7-methanoindene | |
Identifiers | |
3D model (JSmol)
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ChEBI | |
ChEMBL | |
ChemSpider | |
ECHA InfoCard | 100.000.876 |
KEGG | |
PubChem CID
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UNII | |
CompTox Dashboard (EPA)
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Properties | |
C10H5Cl7 | |
Molar mass | 373.32 g/mol |
Appearance | White to tan solid |
Odor | Camphorous |
Density | 1.58 g/cm3 |
Melting point | 95 to 96 °C (203 to 205 °F; 368 to 369 K) |
Boiling point | 135 to 145 °C (275 to 293 °F; 408 to 418 K) at 1-1.5 mmHg |
0.0006% (20°C)[1] | |
Vapor pressure | 0.0003 mmHg (25°C)[1] |
Hazards | |
Flash point | noncombustible[1] |
Lethal dose or concentration (LD, LC): | |
LD50 (median dose)
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116 mg/kg (oral, guinea pig) 40 mg/kg (oral, rat) 100 mg/kg (oral, rat) 68 mg/kg (oral, mouse) 100 mg/kg (oral, hamster)[2] |
LDLo (lowest published)
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50 mg/kg (cat, oral)[2] |
LCLo (lowest published)
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150 mg/m3 (cat, 4 hr) 200 mg/m3 (mammal, 4 hr)[2] |
NIOSH (US health exposure limits): | |
PEL (Permissible)
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TWA 0.5 mg/m3 [skin][1] |
REL (Recommended)
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Ca TWA 0.5 mg/m3 [skin][1] |
IDLH (Immediate danger)
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Ca [35 mg/m3][1] |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Heptachlor is an organochlorine compound that was used as an insecticide. Usually sold as a white or tan powder, heptachlor is one of the cyclodiene insecticides. In 1962, Rachel Carson's Silent Spring questioned the safety of heptachlor and other chlorinated insecticides. Due to its highly stable structure, heptachlor can persist in the environment for decades. In the United States, the Environmental Protection Agency has limited the sale of heptachlor products to the specific application of fire ant control in underground transformers. The amount that can be present in different foods is regulated.[3]