Propoxur
Names | |
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Preferred IUPAC name
2-[(Propan-2-yl)oxy]phenyl methylcarbamate | |
Identifiers | |
CAS Number
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3D model (JSmol)
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ChEBI | |
ChEMBL | |
ChemSpider | |
ECHA InfoCard | 100.003.676 |
KEGG | |
PubChem CID
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UNII | |
CompTox Dashboard (EPA)
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Properties | |
Chemical formula
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C11H15NO3 |
Molar mass | 209.245 g·mol−1 |
Appearance | White to tan crystalline powder[1] |
Odor | faint, characteristic[1] |
Melting point | 86 to 92 °C; 187 to 197 °F; 359 to 365 K |
Boiling point | decomposes[1] |
0.2% (20°C)[1] | |
Vapor pressure | 0.0000937 mmHg (20 °C)[1] |
Pharmacology | |
ATCvet code
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QP53AE02 (WHO) |
Hazards | |
Flash point | > 149 °C; 300 °F; 422 K |
NIOSH (US health exposure limits): | |
PEL (Permissible)
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none[1] |
REL (Recommended)
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TWA 0.5 mg/m3[1] |
IDLH (Immediate danger)
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N.D.[1] |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
what is ?) | (|
Infobox references | |
Propoxur (Baygon) is a carbamate non-systemic insecticide introduced in 1959 with a fast knockdown and long residual effect used against turf, forestry, and household pests and fleas. It is also used in pest control for other domestic animals, Anopheles mosquitoes, ants, gypsy moths, and other agricultural pests.[2][3] It can also be used as a molluscicide.[3][4][5]
Several U.S. states have petitioned the Environmental Protection Agency (EPA) to use propoxur against bedbug infestations, but the EPA has been reluctant to approve indoor use because of its potential toxicity to children after chronic exposure.[6]
Action[]
Carbamate insecticides kill insects by irreversibly inactivating the enzyme acetylcholinesterase.
Environmental effects[]
Propoxur rapidly breaks down in alkaline solution.[7] Propoxur is highly toxic to many bird species, but its toxicity varies by the species. It is moderately to slightly toxic to fish and other aquatic species. Propoxur is highly toxic to honeybees.[5]
References[]
- ^ a b c d e f g h NIOSH Pocket Guide to Chemical Hazards. "#0531". National Institute for Occupational Safety and Health (NIOSH).
- ^ ACGIH, 1991a[full citation needed]
- ^ a b Budavari, 1996a[full citation needed]
- ^ Lewis, 1993a[full citation needed]
- ^ a b EXTOXNET Extension Toxicology Network. Pesticide Information Profile. Propoxur. June 1996.
- ^ "In Search of a Bedbug Solution". New York Times. September 4, 2010.
- ^ Propoxur (WHO Pesticide Residues Series 3): October 01, 2009.
- Acetylcholinesterase inhibitors
- Carbamate insecticides
- Catechol ethers
- Isopropyl compounds
- Aromatic carbamates
- Phenol esters