Fenthion

Fenthion[1]
Names
IUPAC name
O,O-Dimethyl O-[3-methyl-4-(methylsulfanyl)phenyl] phosphorothioate
Other names
• Dimethoxy-[3-methyl-4-(methylthio)phenoxy]-thioxophosphorane
• O,O-Dimethyl O-[3-methyl-4-(methylthio)phenyl] phosphorothioate
• O,O-Dimethyl O-4-methylthio-m-tolyl phosphorothioate
Identifiers
55-38-9 YesY
3D model (Jmol) Interactive image
ChEBI CHEBI:34761 YesY
ChEMBL ChEMBL1604375 N
ChemSpider 3229 YesY
ECHA InfoCard 100.000.211
KEGG D07950 YesY
PubChem 3346
UNII BL0L45OVKT YesY
Properties
C10H15O3PS2
Molar mass 278.33 g/mol
Appearance colorless, almost odorless liquid; 95-98% pure fenthion is a brown oily liquid with a weak garlic odor
Density 1.250 g/cm3 (at 20 °C / 4 °C)
Melting point 7 °C (45 °F; 280 K)
Boiling point 87 °C (189 °F; 360 K) at 0.01 mmHg
54-56 ppm (at 20 °C)
Solubility in glyceride oils, methanol, ethanol, ether, acetone, and most organic solvents, especially chlorinated hydrocarbons soluble
Vapor pressure 4 • 10−5 mmHg (at 20 °C)
Pharmacology
QP53BB02 (WHO)
Hazards
US health exposure limits (NIOSH):
PEL (Permissible)
 none[2]
REL (Recommended)
 None established[2]
IDLH (Immediate danger)
 N.D.[2]
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
N verify (what is YesYN ?)
Infobox references

Fenthion is an organothiophosphate insecticide, avicide, and acaricide. Like most other organophosphates, its mode of action is via cholinesterase inhibition. Due to its relatively low toxicity towards humans and mammals, fenthion is listed as moderately toxic compound in U.S. Environmental Protection Agency and World Health Organization toxicity class.[1][3]

Uses

Fenthion is a contact and stomach insecticide used against many biting insects. It is particularly effective against fruit flies, leaf hoppers, cereal bugs, stem borers, mosquitoes, animal parasites, mites, aphids, codling moths, and weaver birds. It has been widely used in sugar cane, rice, field corn, beets, pome and stone fruit, citrus fruits, pistachio, cotton, olives, coffee, cocoa, vegetables, and vines.[3]

Based on its high toxicity on birds, fenthion has been used to control weaver birds and other pest-birds in many parts of the world. Fenthion is also used in cattle, swine, and dogs to control lice, fleas, ticks, flies, and other external parasites.[3][4][5]

Amid concerns of harmful effects on environment, especially birds, Food and Drug Administration no longer approves uses of fenthion. However, fenthion has been extensively used in Florida to control adult mosquitoes. After preliminary risk assessments on human health and environment in 1998 and its revision in 1999, USEPA issued an Interim Reregistration Eligibility Decision (IRED) for fenthion in January 2001. The EPA has classified fenthion as Restricted Use Pesticide (RUP), and warrants special handling because of its toxicity.[6]

Some common trade names for fenthion are Avigel, Avigrease, Entex, Baytex, Baycid, Dalf, DMPT, Mercaptophos, Prentox, Fenthion 4E, Queletox, and Lebaycid.[3] Fenthion is available in dust, emulsifiable concentrate, granular, liquid concentrate, spray concentrate, ULV, and wettable powder formulations.

Synthesis

Fenthion can be synthesized by condensation of 4-methylmercapto-m-cresol and dimethylphosphorochloridothionate.[1]

Health effects

Fenthion exposure to general population is quite limited based on its bioavailability. Common form of fenthion exposure is occupation related, and occurs through dermal contact or inhalation of dust and sprays.[6] Another likely means of contamination is through ingestion of food, especially, if it has been applied quite recently with fenthion. So far, ingestion is the most likely severe poisoning case on humans and animals.[1] To avoid this, crops applied with fenthion should be allowed enough degradation time before harvesting. Normally, 2 – 4 weeks time is enough depending upon the type of crop.

Fenthion poisoning is consistent with symptoms of other organophosphate effects on human health. Primarily, the effect is cholinesterase inhibition.

Acute toxicity

Acute poisoning of fenthion results in miosis (pinpoint pupils), headache, nausea/vomiting, dizziness, muscle weakness, drowsiness, lethargy, agitation, or anxiety. If the poisoning is moderate or severe, it results in chest tightness, breathing difficulty, hypertension, abdominal pain, diarrhea, heavy salivation, profuse sweating, or fasciculation.[4][6]

Chronic toxicity

Chronic effect of fenthion has not been reported.[6]

Environmental effects

Despite short half-life in the environment, fenthion toxicity is highly significant to birds and estuarine/marine invertebrates.[4] Even though some parts of the world use fenthion to control pest birds, such as weaver bird, many non-targeted wild birds are victim of fenthion poisoning. Acute symptoms of fenthion poisoning in birds include tearing of the eyes, foamy salivation, lack of movement, tremors, congestion of the windpipe, lack of coordination in walking, and an abnormally rapid rate of breathing or difficult breathing. Fenthion has been found toxic to fishes and other aquatic invertebrates. Bees are also found to be greatly affected by fenthion contamination.[3]

Degradation in nature

Photodegradation and biodegradation are common mechanisms of fenthion degradation in the environment. In the atmosphere, vapor phase fenthion reacts rapidly with photochemically produced hydroxyl radicals, and its half-life is about 5 hours. In soil and water, photodegradation is again predominant mechanism if there is enough presence of sunlight. Under normal aquatic environment, half-life of fenthion in water is 2.9 to 21.1 days.[1] It may be photodynamically, chemically or biologically degraded. The degradation mechanisms can be hydrolysis, oxidation, and/or alkylation-dealkylation, which are dependent on the presence of light, temperature, alkali, or enzymatic activity.[7]

In soil, fenthion degradation ranges from 4 to 6 weeks and it occurs through photodegradation as well as anaerobic or non-photolytic organisms. However, soil particles strongly adsorb fenthion that makes it less susceptible to percolate with water through the soil.[6]

References

  1. 1 2 3 4 5 HSDB. (2003). Hazardous Substance Data Bank: Fenthion. National Library of Medicine: National Toxicology Program. Available at http://toxnet.nlm.nih.gov/cgi-bin/sis/htmlgen?HSDB Accessed April 29, 2009.
  2. 1 2 3 "NIOSH Pocket Guide to Chemical Hazards #0285". National Institute for Occupational Safety and Health (NIOSH).
  3. 1 2 3 4 5 EXTOXNET. (2003). Pesticide information Profile for Fenthion. Cooperative Extension Offices of Cornell University, Michigan State University, Oregon State University, and University of California at Davis. Available at http://pmep.cce.cornell.edu/profiles/extoxnet/dienochlor-glyphosate/fenthion-ext.html Accessed April 25, 2009.
  4. 1 2 3 USEPA. (2001). Interim Reregeistration Eligibility Decision for Fenthion. United States Environmental Protection Agency. Available at http://www.epa.gov/pesticides/reregistration/REDs/0290ired.pdf Accessed April 25, 2009.
  5. ↑ APVMA. (2005). Fenthion Review - Frequently asked questions. Australian Pesticides and Veterinary Medicines Authority. Available at http://www.apvma.gov.au/chemrev/fenthion_faq.shtml Accessed April 26, 2009.
  6. 1 2 3 4 5 ASTDR. (2005). Toxicologic Information about Insecticides Used for Eradicating Mosquitoes (West Nile Virus Control). Department of Health and Human Services: Agency for Toxic Substances and Disease Registry. Available at http://www.atsdr.cdc.gov/consultations/west_nile_virus/fenthion.html Accessed April 25, 2009.
  7. ↑ Wang, T., Kadlac, T., and Lenahan, R. (1989). Persistence of Fenthion in the Aquatic Environment. Bull. Environ. Contam. Toxicol., 42 (3), 389-394. doi:10.1007/BF01699965
This article is issued from Wikipedia - version of the 8/24/2016. The text is available under the Creative Commons Attribution/Share Alike but additional terms may apply for the media files.