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Folpet
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Names | |
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Preferred IUPAC name
2-[(Tricloromethyl)sulfanyl]-1H-isoindole-1,3(2H)-dione | |
Other names
N-(Trichloromethylthio)phthalimide, Orthophaltan, Phaltan, Faltan, Folpan, Faltex, Folpex
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Identifiers | |
3D model (JSmol)
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ChEBI | |
ChEMBL | |
ECHA InfoCard | 100.004.627 |
EC Number |
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KEGG | |
PubChem CID
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RTECS number |
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UNII | |
UN number | 3077 2588 |
CompTox Dashboard (EPA)
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Properties | |
C9H4Cl3NO2S | |
Molar mass | 296.55 g·mol−1 |
Appearance | white solid |
Density | 1.72 g/cm3 |
Melting point | 177 °C (351 °F; 450 K) (decomp.) |
Hazards | |
GHS labelling: | |
Warning | |
H317, H319, H332, H351, H400 | |
P201, P202, P261, P264, P271, P272, P273, P280, P281, P302+P352, P304+P312, P304+P340, P305+P351+P338, P308+P313, P312, P321, P333+P313, P337+P313, P363, P391, P405, P501 | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Folpet is the tradename for the organic compound with the formula C6H4(CO)2NSCCl3. It is a fungicide derived from phthalimide (C6H4(CO)2N-) and trichloromethylsulfenyl chloride. The compound is white although commercial samples can appear brownish. It is structurally related to Captan, which is also a trichloromethylsulfenyl-containing fungicide.
Resistance
As of December 2019 folpet resistance is still unheard of due to its multiple effects. However, in 2001 some degree of cross-resistance was reported in iprodione-resistant South African Botrytis cinerea on grape.