Fenitrothion

Source: Wikipedia, the free encyclopedia.
Fenitrothion
Names
Preferred IUPAC name
O,O-Dimethyl O-(3-methyl-4-nitrophenyl) phosphorothioate
Other names
• Dimethoxy-(3-methyl-4-nitrophenoxy)thioxophosphorane
O,O-Dimethyl O-4-nitro-m-tolyl phosphorothioate
Identifiers
3D model (
JSmol
)
ChEBI
ChEMBL
ChemSpider
ECHA InfoCard
100.004.114 Edit this at Wikidata
KEGG
UNII
  • InChI=1S/C9H12NO5PS/c1-7-6-8(4-5-9(7)10(11)12)15-16(17,13-2)14-3/h4-6H,1-3H3 checkY
    Key: ZNOLGFHPUIJIMJ-UHFFFAOYSA-N checkY
  • InChI=1/C9H12NO5PS/c1-7-6-8(4-5-9(7)10(11)12)15-16(17,13-2)14-3/h4-6H,1-3H3
    Key: ZNOLGFHPUIJIMJ-UHFFFAOYAZ
  • S=P(Oc1cc(c(cc1)[N+]([O-])=O)C)(OC)OC
Properties
C9H12NO5PS
Molar mass 277.23 g·mol−1
Appearance Yellow-brown liquid
Density 1.3227 g/cm3
Melting point 3.4 °C (38.1 °F; 276.5 K)
Boiling point 118 °C (244 °F; 391 K) at 0.05 mmHg
38.0 mg/L
Solubility Readily soluble in dichloromethane, 2-propanol, toluene, hardly soluble in n-hexane.[1]
log P 3.30 (octanol/water)[2]
Hazards
Lethal dose or concentration (LD, LC):
Rat, oral: 500 mg/kg[3]

Mouse (female), oral: 1416 mg/kg[4]

Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
checkY verify (what is checkY☒N ?)

Fenitrothion (

phosphorothioate (organophosphate) insecticide that is inexpensive and widely used worldwide. Trade names include Sumithion, a 94.2% solution of fenitrothion.[5]

Health effects

Fenitrothion at sublethal doses affected the motor movement of marsupials,[6] and at acute dose levels it reduced the energy of birds.[7]

In chronic (low) dose tests, unexpectedly only the lowest concentration (0.011 microgram/liter) of fenitrothion depressed the growth of an algae, though all of the chronic dose levels used were toxic in other ways to the algae.[8]

Just half of fenitrothion's minimally effective dose altered the thyroid structure of a freshwater murrel (the snakehead fish).[9]

Cases of non-specific

Reye's syndrome) in children living in the vicinity of fenitrothion-spraying operations invoked the research described latterly in Science,[10] and originally in The Lancet:[11]

2-day-old mice were dosed topically for 11 days with fenitrothion, amongst other substances. After a further 2 days a sublethal dose of

encephalomyocarditis virus was injected subcutaneously in known titre. Mortality-rates in the 10-day period after virus
injection 4-9% in fenitrothion groups, and 0% in corn-oil controls. Fatty changes were noted in liver and kidney in the insecticide-virus groups. The encephalopathy showed no specific central-nervous system lesion, but death followed a sequence of paralysis and convulsions. The possible role of exposure to combinations of insecticides in human viral susceptibility requires further attention.

Further study showed that the illness was caused not by fenitrothion itself, but combinations which included the surfactants and the solvent (with or without the pesticide) clearly showed that pretreatment with these chemicals markedly increased the viral lethality in the test mice.[12]

Resistance

In an unusual demonstration of resistance to pesticides, 8% of insects in farm fields were found to carry a symbiotic gut microbe that can metabolize and detoxify fenitrothion; after in-vitro tests showed that the microbe significantly increased the survival of fenitrothion-treated insects.[13]

References

  1. OCLC 50201739
    .
  2. .
  3. .
  4. ^ Sekizawa J, Eto M, Miyamoto J, Matsuo M (1992). Environ Health Criteria 133: Fenitrothion (Report). Geneva: World Health Organization. p. 70.
  5. ^ "Fenitrothion". PubChem Compound Database. National Center for Biotechnology Information.
  6. PMID 18547601
    .
  7. .
  8. .
  9. .
  10. .
  11. .
  12. .
  13. .

Further reading

External links