Thiophanate-methyl

Thiophanate-methyl
Names
	IUPAC name Dimethyl 4,4′-(o-phenylene)bis(3-thioallophanate)
Identifiers
CAS Number	23564-05-8 ;
3D model (JSmol)	Interactive image;
ChemSpider	2297683;
ECHA InfoCard	100.041.567
PubChem CID	3032791;
UNII	K4N81R84L8 ;
CompTox Dashboard (EPA)	DTXSID1024338 ;
	InChI InChI=1S/C12H14N4O4S2/c1-19-11(17)15-9(21)13-7-5-3-4-6-8(7)14-10(22)16-12(18)20-2/h3-6H,1-2H3,(H2,13,15,17,21)(H2,14,16,18,22) Key: QGHREAKMXXNCOA-UHFFFAOYSA-N;
	SMILES COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC;
Properties
Chemical formula	C12H14N4O4S2
Molar mass	342.39 g·mol−1
Appearance	white powder
Melting point	172 °C (342 °F; 445 K)
Solubility in water	26.6 mg/L
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
	Infobox references

Thiophanate-methyl is an organic compound with the formula C₆H₄(NHC(S)NH(CO)OCH₃)₂. The compound is a colorless or white solid, although commercial samples are generally tan-colored. It is prepared from o-phenylenediamine.

Uses and analysis

It is a widely used fungicide used on tree, vine, and root crops.[1] In Europe it is applied to tomato, wine grapes, beans, wheat, and aubergine.[2]

Methods for its analysis have received considerable attention.[3][4][5]

References

"Thiophanate-methyl" (PDF). Environmental Protection Agency.
. doi:10.2903/j.efsa.2018.5133 //doi.org/10.2903%2Fj.efsa.2018.5133. Cite journal requires |journal= (help); Missing or empty |title= (help)
Mol, Hans G. J.; Plaza-BolañOs, Patricia; Zomer, Paul; De Rijk, Theo C.; Stolker, Alida A. M.; Mulder, Patrick P. J. (2008). "Toward a Generic Extraction Method for Simultaneous Determination of Pesticides, Mycotoxins, Plant Toxins, and Veterinary Drugs in Feed and Food Matrixes". Analytical Chemistry. 80 (24): 9450–9459. doi:10.1021/ac801557f. PMID 19072261.
Romero-González, R.; Garrido Frenich, A.; Martínez Vidal, J.L.; Prestes, O.D.; Grio, S.L. (2011). "Simultaneous determination of pesticides, biopesticides and mycotoxins in organic products applying a quick, easy, cheap, effective, rugged and safe extraction procedure and ultra-high performance liquid chromatography–tandem mass spectrometry". Journal of Chromatography A. 1218 (11): 1477–1485. doi:10.1016/j.chroma.2011.01.034. PMID 21292276.
Kiljanek, Tomasz; Niewiadowska, Alicja; Semeniuk, Stanisław; Gaweł, Marta; Borzęcka, Milena; Posyniak, Andrzej (2016). "Multi-residue method for the determination of pesticides and pesticide metabolites in honeybees by liquid and gas chromatography coupled with tandem mass spectrometry—Honeybee poisoning incidents". Journal of Chromatography A. 1435: 100–114. doi:10.1016/j.chroma.2016.01.045. PMID 26830634.

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[1] "Thiophanate-methyl" (PDF). Environmental Protection Agency.

[2] . doi:10.2903/j.efsa.2018.5133 //doi.org/10.2903%2Fj.efsa.2018.5133. Cite journal requires |journal= (help); Missing or empty |title= (help)

[3] Mol, Hans G. J.; Plaza-BolañOs, Patricia; Zomer, Paul; De Rijk, Theo C.; Stolker, Alida A. M.; Mulder, Patrick P. J. (2008). "Toward a Generic Extraction Method for Simultaneous Determination of Pesticides, Mycotoxins, Plant Toxins, and Veterinary Drugs in Feed and Food Matrixes". Analytical Chemistry. 80 (24): 9450–9459. doi:10.1021/ac801557f. PMID 19072261.

[4] Romero-González, R.; Garrido Frenich, A.; Martínez Vidal, J.L.; Prestes, O.D.; Grio, S.L. (2011). "Simultaneous determination of pesticides, biopesticides and mycotoxins in organic products applying a quick, easy, cheap, effective, rugged and safe extraction procedure and ultra-high performance liquid chromatography–tandem mass spectrometry". Journal of Chromatography A. 1218 (11): 1477–1485. doi:10.1016/j.chroma.2011.01.034. PMID 21292276.

[5] Kiljanek, Tomasz; Niewiadowska, Alicja; Semeniuk, Stanisław; Gaweł, Marta; Borzęcka, Milena; Posyniak, Andrzej (2016). "Multi-residue method for the determination of pesticides and pesticide metabolites in honeybees by liquid and gas chromatography coupled with tandem mass spectrometry—Honeybee poisoning incidents". Journal of Chromatography A. 1435: 100–114. doi:10.1016/j.chroma.2016.01.045. PMID 26830634.