Names | |
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IUPAC name
S-Benzyl N,N-dipropylcarbamothioate
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Other names
Prosulfocarb, A8545C
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Identifiers | |
ECHA InfoCard | 100.100.363 |
PubChem CID
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CompTox Dashboard (EPA)
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Properties | |
C14H21NOS | |
Molar mass | 251.39 g·mol−1 |
Appearance | Colourless - pale yellow |
Odor | Aromatic |
Density | 1049 kg/m3[1] |
Melting point | -20 °C[3] |
Boiling point | 341 °C[3] |
Insoluble[3] | |
Solubility in xylene | Soluble[3] |
Solubility in acetone | Soluble[3] |
Solubility in heptane | Soluble[3] |
Solubility in ethyl acetate | Soluble[3] |
Vapor pressure | 0.79 mPa[3] |
Hazards | |
GHS labelling: | |
Warning | |
H227, H302, H317, H335, H371, H373, H401 | |
Flash point | 167.1 °C[1] |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Prosulfocarb is a pre-emergent herbicide used agriculturally in Australia, the EU, Japan, New Zealand, (since 2020), Morocco and Iran, for control of annual ryegrass and toad rush in wheat and barley crops.[4][5][6][3] It was introduced to the EU in 1988 and is rapidly growing in use, with sales increasing by over 500% in France since 2008.[7]
Prosulfocarb is a thiocarbamate, and is absorbed by the roots of germinating seedlings to inhibit growth in the meristem by inhibiting fat synthesis,[4] of resistance HRAC Group J, (Aus),[4] K3/N, (Global), 15. (numeric)[8] Applying prosulfocarb repeatedly builds weed resistance but undoes trifluralin (Group 3) resistance, as they have opposing mechanisms: prosulfocarb is resisted by decreasing pesticide metabolism; trifluralin is resisted by increasing metabolism.[9]
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was invoked but never defined (see the help page).