Details
Stereochemistry | ACHIRAL |
Molecular Formula | C15H16F3N5O4S |
Molecular Weight | 419.379 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
COC1=NC(C)=NC(NC(=O)NS(=O)(=O)C2=C(CCC(F)(F)F)C=CC=C2)=N1
InChI
InChIKey=LTUNNEGNEKBSEH-UHFFFAOYSA-N
InChI=1S/C15H16F3N5O4S/c1-9-19-12(22-14(20-9)27-2)21-13(24)23-28(25,26)11-6-4-3-5-10(11)7-8-15(16,17)18/h3-6H,7-8H2,1-2H3,(H2,19,20,21,22,23,24)
Molecular Formula | C15H16F3N5O4S |
Molecular Weight | 419.379 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Prosulfuron is a broad-spectrum sulfonylurea herbicide approved for use at EU for selective control of broadleaf weeds in corn, sorghum, and cereal grains. It is highly soluble in water and many organic solvents. Prosulfuron is volatile, mobile and has a high potential for leaching to groundwater. Prosulfuron is subject to numerous aryl and aliphatic hydroxylation reactions in microbial cultures, plants, and animals. Other degradative reactions include O-demethylation of the triazinyl methoxy group and cleavage of the sulfonylurea linkage of the parent herbicide and hydroxylated metabolites. It is generally moderately persistent in soil systems but can very persistent in aquatic systems. It is moderately toxic to mammals birds, honeybees, earthworms and fish but is not expected to bioaccumulate. Prosulfuron has rapidly eliminated in mammals. In rats treated with subtoxic doses of Prosulfuron 90% of the oral dose excreted within 48 hours. No significant residues were found in tissues collected 7 days after dosing, and unmetabolized Prosulfuron represented a significant portion of the excreted radiolabelled residues. Prosulfuron is highly toxic to algae and aquatic plants.
Approval Year
PubMed
Title | Date | PubMed |
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Soil transformation of prosulfuron. | 2003 Jun 4 |
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Factors controlling sorption of prosulfuron by variable-charge soils and model sorbents. | 2004 Jul-Aug |
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[Simultaneous determination of ten sulfonylurea herbicide residues in soybeans by high performance liquid chromatography]. | 2004 Nov |
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Hydrophilic and hydrophobic sorption of organic acids by variable charge soils: effect of chemical acidity and acidic functional group. | 2004 Oct 15 |
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No-tillage system applied to the sunflower (hybrid pioneer PR64E83) resistant to the tribenuron-methyl in the conditions from Romania. | 2007 |
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A composite transcriptional signature differentiates responses towards closely related herbicides in Arabidopsis thaliana and Brassica napus. | 2010 Mar |
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N-methylimidazolium ionic liquid-functionalized silica as a sorbent for selective solid-phase extraction of 12 sulfonylurea herbicides in environmental water and soil samples. | 2010 Mar 5 |
Patents
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 18:06:36 GMT 2023
by
admin
on
Fri Dec 15 18:06:36 GMT 2023
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Record UNII |
NG7LE47J14
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Record Status |
Validated (UNII)
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Record Version |
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-
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EPA PESTICIDE CODE |
129031
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94125-34-5
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prosulfuron
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DTXSID9034868
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m9262
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NG7LE47J14
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91751
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