Tetrachlorvinphos
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| Names | |
|---|---|
| Preferred IUPAC name
(Z)-2-Chloro-1-(2,4,5-trichlorophenyl)ethen-1-yl dimethyl phosphate | |
| Other names | |
| Identifiers | |
CAS Number |
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3D model (JSmol) |
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Beilstein Reference |
1890909 |
| ChEBI | |
| ChEMBL | |
| ChemSpider | |
| ECHA InfoCard | 100.040.772 |
| EC Number |
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| KEGG | |
PubChem CID |
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| RTECS number |
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| UNII | |
| UN number | 2783 |
CompTox Dashboard (EPA) |
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InChI
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SMILES
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| Properties | |
Chemical formula |
C10H9Cl4O4P |
| Molar mass | 365.95 g·mol−1 |
| Melting point | 97 to 98 °C (207 to 208 °F; 370 to 371 K)[4] |
| Pharmacology | |
| QP53AF14 (WHO) QP53BB04 (WHO) | |
| Hazards | |
| GHS labelling: | |
Pictograms |
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Signal word |
Warning |
Hazard statements |
H302, H332, H410 |
Precautionary statements |
P261, P264, P270, P271, P273, P301+P312, P304+P312, P304+P340, P312, P330, P391, P501 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references | |
Tetrachlorvinphos is an organophosphate insecticide used to kill fleas and ticks.[2]
History
Tetrachlorvinphos was initially registered for use in the United States in 1966 by the U.S. Department of Agriculture. Tetrachlorvinphos was originally registered for use on various food crops, livestock, pet animals, and in or around buildings. The crop uses were voluntarily canceled from product registrations in 1987.[5] In 2014, the Natural Resources Defense Council (NRDC) filed a lawsuit against the United States Environmental Protection Agency (EPA) seeking EPA to respond to NRDC's 2009 petition to ban tetrachlorvinphos in common pet flea treatment products.[6][7]
Human health hazards
Symptoms of exposure to this material include increased perspiration, nausea, lachrymation, salivation, blurred vision, diarrhea, pulmonary edema, respiratory depression and convulsions. The chemical material may be absorbed through the skin and is a lachrymator. It is a cholinesterase inhibitor and is a positive animal carcinogen.[3]
Chemical properties
The substance is insoluble in water. Flash point data are not available for this chemical; however, it is probably combustible. Tetrachlorvinphos is slowly hydrolyzed in neutral and aqueous acidic media. Is rapidly hydrolyzed in alkaline media.[3]
References
- ↑ "tetrachlorvinphos data sheet". www.bcpcpesticidecompendium.org. BCP Pesticide Compendium.
- 1 2 "Tetrachlorvinphos (TCVP)". Natural Resources Defense Council.
- 1 2 3 "TETRACHLORVINPHOS | CAMEO Chemicals | NOAA".
- ↑ "Tetrachlorvinphos". Sigma-Aldrich.
- ↑ "EPA Factsheet" (PDF). Archived from the original (PDF) on 2014-08-09. Retrieved 2013-07-28.
- ↑ "EPA Sued Over Toxic Pesticides in Pet Flea Collars | EcoWatch". ecowatch.com. Archived from the original on 2014-02-09.
- ↑ "NRDC Sues EPA to Ban Two Toxic Pesticides in Pet Flea Collars".
This article contains public domain text from the EPA and the NOAA .
External links
- Tetrachlorvinphos (TCVP), Environmental Protection Agency
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