Demeton-S-methyl

Last updated
Demeton-S-methyl [1]
Demeton-S-methyl.png
Names
Preferred IUPAC name
S-[2-(Ethylsulfanyl)ethyl] O,O-dimethyl phosphorothioate
Other names
1-(Dimethoxyphosphorylthio)-2-(ethylthio)ethane
S-[2-(Ethylthio)ethyl] O,O-dimethyl phosphorothioate, Demeton methyl; O,O-Dimethyl 2-ethylmercaptoethyl thiophosphate; Metasystox; Methyl mercaptophos; Methyl systox
Identifiers
3D model (JSmol)
1707311
ChEBI
ChEMBL
ChemSpider
ECHA InfoCard 100.011.866 OOjs UI icon edit-ltr-progressive.svg
EC Number
  • 213-052-6
KEGG
PubChem CID
RTECS number
  • TG1750000
UNII
UN number 3018
  • InChI=1S/C6H15O3PS2/c1-4-11-5-6-12-10(7,8-2)9-3/h4-6H2,1-3H3 Yes check.svgY
    Key: WEBQKRLKWNIYKK-UHFFFAOYSA-N Yes check.svgY
  • InChI=1/C6H15O3PS2/c1-4-11-5-6-12-10(7,8-2)9-3/h4-6H2,1-3H3
    Key: WEBQKRLKWNIYKK-UHFFFAOYAF
  • O=P(OC)(SCCSCC)OC
Properties
C6H15O3PS2
Molar mass 230.28 g/mol
AppearanceOily, colorless to pale-yellow liquid [2]
Density 1.2 g/cm3
Boiling point 118 °C (244 °F; 391 K)
0.33 g/100 ml (20 °C (68 °F; 293 K))
Vapor pressure 0.0004 mmHg (20 °C (68 °F; 293 K)) [2]
Hazards
GHS labelling:
GHS-pictogram-skull.svg GHS-pictogram-pollu.svg
Danger
H301, H311, H411
P264, P270, P273, P280, P301+P310, P302+P352, P312, P321, P322, P330, P361, P363, P391, P405, P501
NIOSH (US health exposure limits):
PEL (Permissible)
N.D. [2]
REL (Recommended)
TWA 0.5 mg/m3 [skin] [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).
Yes check.svgY  verify  (what is  Yes check.svgYX mark.svgN ?)

Demeton-S-methyl is an organic compound with the molecular formula C6H15O3PS2. It was used as an organothiophosphate acaricide and organothiophosphate insecticide. It is flammable. With prolonged storage, Demeton-S-methyl becomes more toxic due to formation of a sulfonium derivative which has greater affinity to the human form of the acetylcholinesterase enzyme, and this may present a hazard in agricultural use. [3]

Contents

History

Demeton-S-methyl was first described in 1950 by Schrader and was widely adopted as a pesticide because of the lower toxicity to humans than the previously used demeton. [4] [5] In its beginning days, it was mostly used together with demeton-O-methyl in an O:S ratio of 70:30. From 1957 onward, only pure demeton-S-methyl was used. [6] Because of its high toxicity and severe toxic effects to humans, demeton-S-methyl is now classified as a highly toxic substance by the World Health Organization and is banned from agricultural use worldwide. [7] [8]

Structure and reactivity

Demeton-S-Methyl is a compound that is closely related to VX in terms of structure. The structure is C6H15O3PS2. Demeton-S-Methyl has a molecular weight of 230.28 g/mol. [9] It appears as a colourless to slightly yellow coloured oily liquid with a garlic like odor. [10] Its density is 1.2 g/cm3, which makes it slightly heavier than water. The melting points and boiling points are <25 °C (<77 °F) and 118 °C (244 °F) respectively, [11] although the compound decomposes before reaching the boiling point. The relatively low 0,0004 mmHg (at 20 °C (68 °F; 293 K)) [12] means Demeton-S-Methyl will vaporize very slowly and mostly stay as a liquid. Demeton-S-Methyl is less stable than its predecessor Demeton, but it is used instead because of the lower toxicity to humans. Demeton-S-methyl is hydrolyzed quickly in alkaline media. [13] Demeton-S-methyl is readily soluble in water and most organic compounds.

Synthesis

There are three ways of synthesizing Demeton-S-methyl. It can be made by a reaction between Thiodiglycol and dimethyl thiophosphate. [14] Here the sulfur in dimethyl thiophosphate attacks on one of the oxygens of thiodiglycol. One of the oxygens of dimethyl thiophosphate in turn forms a double bond with the phosphate and losing its hydrogen which forms water with the hydroxyl on the other side of the thiodiglycol. The second synthesis route is by alkylation of Dimethyl dithiophosphoric acid with 2-(ethylmercapto)-ethyl chloride. [15] The third way is through  the reaction of 2-(ethylthio)-ethanol, which is similar to thiodiglycol minus one of the hydroxyl groups, and O,O-dimethyl phosphochlorothioate. This happens through alcohol chlorination, hydrolysis and dehydrochlorination respectively. [16]

Available forms

Demeton-S-methyl is still available as a solution, however its use is banned in most countries because of the severe toxicity.

Mechanism of action

Demeton-S-methyl inhibits cholinesterase, which takes care of the breakdown of acetylcholine (AChE). In the presence of Demeton-S-methyl, an accumulation of AChE occurs, which can result in impeded neurotransmission. [17] This can lead to impaired muscle function and even suffocation resulting in death. [18]

Metabolism

Animal experiments show that almost all demeton-S-methyl derivatives are excreted through urine. Most of the demeton-S-methyl is converted to demeton-S-methyl sulfoxide, where an oxygen group is added to the sulfur in the side chain. This sulfoxide can then be further metabolised by adding another oxygen group, creating demeton-S-methyl sulfone. Another pathway to metabolise demeton-S-methyl is to demethylate the oxygen group(s) of demeton. Again, this demethylated form can occur in an sulfoxide and sulfone form. Lastly, de-esterification of the O-methylphosphoric ester group can occur which will be followed by methylation and sulfoxidation. This will lead to the formation of methyl sulfinyl-2-ethyl sulfinyl ethane and methyl sulfinyl-2-ethyl sulfonyl ethane. [19]

Uses

Demeton-S-Methyl is an organic phosphorus compound that has been used as an effective insecticide and acaricide in agriculture, mainly against plant-sucking arthropod pests. [20] [21] It was applied for control of aphids, mites, and whiteflies on fruit, vegetables, potatoes, beet and hops. [22] Demeton-S-Methyl is absorbed and distributed within the plant, allowing concentrations to reach high enough levels to kill the insects that feed on the plant by sucking its juices.

In agriculture, methyl demeton was used in a mixture of the O-isomer and the S-isomer in an approximate ratio of 70:30. [23] However, the S-isomer was found to be more toxic against insects than the O-isomer. [24] When the purified S-isomer form was introduced and availability rose, it replaced the mixture in agriculture.

Effects on human health

A lot of data on the toxicity of methyl-S-demeton comes from case studies, often with persons who have been exposed to the chemical occupationally. Methyl-S-demeton was sprayed on the plants by sprayers, who were often temporarily employed. In a study with sprayers that used methyl-S-demeton occupationally the health implications were assessed. [25] The sprayers worked 8 hours a day, and symptoms of intoxication occurred after one to 18 days of exposure. The main signs of toxicity included drowsiness, vomiting, abdominal pain, diarrhoea, nausea, fatigue, headache, respiratory problems, salivation and lachrymation. Serum-cholinesterase levels were lowered by 64% in 25 sprayers when compared to control persons.

In one case of poisoning, ingestion of 50 to 500 mg of methyl-S-demeton/kg body weight resulted in acute cardiovascular collapse and death 83 hours after exposure. [23] A second case-study involves a farmer who was exposed to the chemical on at least 23 occasions for periods varying from 20 minutes to 6+3⁄4 hours, mostly during his work as a marker in aerial spraying but also during the preparation of the chemical. [26] He developed headaches, nausea and dizziness during the working week which subsided during the weekend. Later, he developed anorexia and had difficulty performing simple cognitive tasks. He was admitted to the hospital where it was found that his serum-cholinesterase levels were very low. He was discharged when these levels rose to acceptable levels. In another case, a two-year-old boy was admitted to the hospital after ingestion of 10 ml (0.35 imp fl oz; 0.34 US fl oz) of demeton-S-methyl. Symptoms included excessive salivation, vomiting, bronchial hypersecretion, muscarinic effects on pulse rate and pupil size, and slight bradycardia. [27] In this case, too, serum-cholinesterase levels were significantly lowered, but returned to baseline after admission to the hospital. Lastly, one case of lethal suicide intoxication with demeton-S-methyl has been reported. [28]

Toxicity

The Joint FAO/WHO Meeting on Pesticide Residues (JMPR) concluded that demeton-S-methyl is a highly toxic organophosphorus insecticide. Effects due to chronic exposure are unlikely to occur. Furthermore, demeton-S-methyl does not persist in the environment and is not accumulated by organisms. However, demeton-S-methyl has a high acute toxicity towards aquatic invertebrates and is also toxic to birds and fish. [17] The JMPR recommended ADI (acceptable daily intake) is 0.0003 mg/kg body weight. The LD50 values of demeton-S-methyl for mammals range from 7 to 100 mg/kg body weight, depending on the route of administration and species. [17]

Oral LD50 values of demeton-S-methyl in rats were between 33 and 129 mg/kg body weight. [17] When the toxin was inhaled, the LC50 with 4 hours of exposure for Wistar rats was found to be 310 mg/m3 air for males, and 210 mg/m3 air for females. [17] In dietary studies on dogs, mice and rats, NOAEL (No Observed Adverse Effect Level) values of 1 mg/kg diet were found. These values are equal to a NOAEL range of 0.036 to 0.24 mg/kg body weight per day.

Analysis

Hrynko et al. 2021 provides an analysis method for detection of Demeton-S-methyl and Demeton-S-methyl-sulfone intoxication of bees. [29]

See also

Related Research Articles

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References

  1. ↑ Demeton-S-methyl at INCHEM
  2. 1 2 3 4 5 NIOSH Pocket Guide to Chemical Hazards. "#0410". National Institute for Occupational Safety and Health (NIOSH).
  3. ↑ Black RM, Harrison JM. The chemistry of organophosphorus chemical warfare agents. Chapter 10 of The chemistry of organophosphorus compounds. Volume 4, Ter- and quinque-valent phosphorus acids and their derivatives. (1996) ISBN   0-471-95706-2
  4. ↑ Fest, Christa; Schmidt, Karl-Julius (1973). The Chemistry of Organophosphorus Pesticides. doi:10.1007/978-3-642-97876-0. ISBN   978-3-642-97878-4.
  5. ↑ Matolcsy, György (1988). Pesticide chemistry. Miklós. Nádasy, Viktor Andriska, Sándor Terényi. Amsterdam: Elsevier. ISBN   978-0-444-98903-1. OCLC   316571303.
  6. ↑ "Advisory Report Health-based Reassessment of Administrative Occupational Exposure Limits; Methyl-S-demeton" (PDF).
  7. ↑ "The WHO Recommended Classification of Pesticides by Hazard and guidelines to classification, 2019 edition". World Healthy Organization (WHO). Retrieved 2022-06-15.
  8. ↑ "Pesticide Restricitions".
  9. ↑ "CDC - NIOSH Pocket Guide to Chemical Hazards - Demeton".
  10. ↑ "Hazardous Substances Data Bank (HSDB)".
  11. ↑ "919-86-8 CAS MSDS (DEMETON-S-METHYL) Melting Point Boiling Point Density CAS Chemical Properties".
  12. ↑ "NOAA Office of Response. Search Chemicals".
  13. ↑ Tomlin, C.D.S., "Demeton-S-Methyl 919-86-8", The e-Pesticide Manual, 13th Edition Version 3.1, British Crop Protection Council
  14. ↑ Koch, R. (1982). "Sittig, M., Pesticide Manufacturing and Toxic Materials Control Encyclopedia. Park Ridge, N. J., Noyes Data Corporation, 1980, 810 S., 96.–$". Acta Hydrochimica et Hydrobiologica . 10 (4): 338. doi:10.1002/aheh.19820100405. ISSN   0323-4320.
  15. ↑ Spencer, E.Y. (1982). Guide to the Chemicals Used in Crop Protection (7th ed.). Ottawa, Canada: Information Canada. p. 169.
  16. ↑ Ashford, R.D. (1994). Ashford's Dictionary of Industrial Chemicals. Benezit Dictionary of Artists. Wavelength Publications Ltd.
  17. 1 2 3 4 5 World Health Organization/International Programme on Chemical Safety. DemetonS-methyl. Geneva, Switzerland: World Health Organization, 1997; Environmental Health Criteria 197.
  18. ↑ "Active Ingredient Fact Sheets" (PDF).
  19. ↑ "697. Demeton-S-methyl (Pesticide residues in food: 1984 evaluations)".
  20. ↑ Bishop, AL; McKenzie, HJ; Barchia, IM; Spohr, LJ (April 1998). "Efficacy of insecticides against the lucerne flea, Sminthurus viridis (L.) (Collembola: Sminthuridae), and other arthropods in lucerne". Australian Journal of Entomology . 37 (1): 40–48. doi:10.1111/j.1440-6055.1998.00019.x. ISSN   1326-6756.
  21. ↑ Ziegler, Walter; Engelhardt, Gabriele; Wallnoefer, Peter R.; Oehlmann, Linthard; Wagner, Klaus (November 1980). "Degradation of demeton S-methyl sulfoxide (Metasystox R) by soil microorganisms". Journal of Agricultural and Food Chemistry . 28 (6): 1102–1106. doi:10.1021/jf60232a003. ISSN   0021-8561.
  22. ↑ Spencer, E.Y. (December 1984). "The pesticide manual-A world compendium. 7th ed". Pesticide Biochemistry and Physiology . 22 (3): 369. doi:10.1016/0048-3575(84)90030-0. ISSN   0048-3575.
  23. 1 2 "Health Council of the Netherlands: Committee on Updating of Occupational Exposure Limits. Methyl-S-demeton; Health-based Reassessment of Administrative Occupational Exposure Limits". Health Council of the Netherlands . 2003.
  24. ↑ Chambers, Janice E. (1992), "Summary and Conclusions", Organophosphates Chemistry, Fate, and Effects, Elsevier, pp. 435–440, doi:10.1016/b978-0-08-091726-9.50026-4, ISBN   9780080917269
  25. ↑ Hegazy, M. R. (1965-07-01). "Poisoning by Meta-Isosystox in Spraymen and in Accidentally Exposed Patients". Occupational and Environmental Medicine . 22 (3): 230–235. doi:10.1136/oem.22.3.230. ISSN   1351-0711. PMC   1008302 .
  26. ↑ Redhead, I.H. (March 1968). "Poisoning on the Farm". The Lancet . 291 (7544): 686–688. doi:10.1016/s0140-6736(68)92117-x. ISSN   0140-6736. PMID   4170666.
  27. ↑ Rolfsjord, L. B., Fjaerli, H. O., Meidel, N., Stromme, J. H., Kowalczyk, M., & Jacobsen, D. (1998). "Severe organophosphate (demeton-S-methyl) poisoning in a two-year-old child". Veterinary and Human Toxicology . 40 (4): 222–224. PMID   9682409.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  28. ↑ Schludecker, D.; Aderjan, R. (August 1988). "Chemisch-Toxikologische Befunde bei einer tödlich verlaufenen suicidalen Vergiftung mit Demeton-S-Methyl". Zeitschrift für Rechtsmedizin . 101 (1): 55–60. doi:10.1007/bf00205326. ISSN   0044-3433. PMID   3218390. S2CID   37340261.
  29. ↑ Hrynko, Izabela; Kaczyński, Piotr; Łozowicka, Bożena (2021). "A global study of pesticides in bees: QuEChERS as a sample preparation methodology for their analysis – Critical review and perspective". Science of the Total Environment . Elsevier BV. 792: 148385. Bibcode:2021ScTEn.792n8385H. doi:10.1016/j.scitotenv.2021.148385. ISSN   0048-9697. PMID   34153771. This review cites this research: Hrynko, Izabela; Łozowicka, Bożena; Kaczyński, Piotr (2021). "Development of precise micro analytical tool to identify potential insecticide hazards to bees in guttation fluid using LC–ESI–MS/MS". Chemosphere . Elsevier BV. 263: 128143. Bibcode:2021Chmsp.263l8143H. doi:10.1016/j.chemosphere.2020.128143. ISSN   0045-6535. PMID   33297131. S2CID   224994184.
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