In this article, we will delve into the fascinating world of Fenamiphos, exploring its origins, evolution and relevance today. From its appearance in history to its impact on contemporary society, Fenamiphos has played a fundamental role in different aspects of our lives. Along these lines, we will delve into its most relevant and transcendental aspects, analyzing its influence in various areas and its importance in popular culture. Join us on this journey of discovery and reflection about Fenamiphos, an exciting topic that will not leave anyone indifferent.
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Names | |
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Preferred IUPAC name
(RS)-N-propan-2-amine | |
Systematic IUPAC name
(RS)-{Ethoxyphosphoryl}(propan-2-yl)amine | |
Identifiers | |
3D model (JSmol)
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4752893 | |
ChEBI | |
ChEMBL | |
ChemSpider |
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ECHA InfoCard | 100.040.756 |
EC Number |
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KEGG | |
MeSH | Fenamiphos |
PubChem CID
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RTECS number |
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UNII | |
UN number | 2783, 2811 |
CompTox Dashboard (EPA)
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Properties | |
C13H22NO3PS | |
Molar mass | 303.36 g·mol−1 |
Appearance | Off-white to tan waxy solid |
Density | 1.14 g/cm3[1] |
Melting point | 49 °C; 121 °F; 323 K[1] |
0.03% (20 °C)[1] | |
Vapor pressure | 0.00005 mmHg (20 °C)[1] |
Hazards | |
Occupational safety and health (OHS/OSH): | |
Main hazards
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Toxic |
NIOSH (US health exposure limits): | |
PEL (Permissible)
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none[1] |
REL (Recommended)
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TWA 0.1 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 , 100 kPa).
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Fenamiphos is an organophosphate acetylcholinesterase inhibitor used as an insecticide.[2]