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 |
|---|---|---|
| N-methylimidazolium ionic liquid-functionalized silica as a sorbent for selective solid-phase extraction of 12 sulfonylurea herbicides in environmental water and soil samples. | 2010-03-05 |
|
| A composite transcriptional signature differentiates responses towards closely related herbicides in Arabidopsis thaliana and Brassica napus. | 2010-03 |
|
| Non-antibiotic selection systems for soybean somatic embryos: the lysine analog aminoethyl-cysteine as a selection agent. | 2009-11-18 |
|
| Organic amendments from olive cake as a strategy to modify the degradation of sulfonylurea herbicides in soil. | 2007-07-25 |
|
| No-tillage system applied to the sunflower (hybrid pioneer PR64E83) resistant to the tribenuron-methyl in the conditions from Romania. | 2007 |
|
| Impact of an herbicide combination of bromoxynil and prosulfuron on soil microorganisms. | 2006-09 |
|
| [Simultaneous determination of ten sulfonylurea herbicide residues in soybeans by high performance liquid chromatography]. | 2004-11 |
|
| Hydrophilic and hydrophobic sorption of organic acids by variable charge soils: effect of chemical acidity and acidic functional group. | 2004-10-15 |
|
| Factors controlling sorption of prosulfuron by variable-charge soils and model sorbents. | 2004-07-16 |
|
| Crosstalk and differential response to abiotic and biotic stressors reflected at the transcriptional level of effector genes from secondary metabolism. | 2004-04 |
|
| Soil transformation of prosulfuron. | 2003-06-04 |
|
| Effects of soil pH and soil water content on prosulfuron dissipation. | 2002-05-22 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 19:02:30 GMT 2025
by
admin
on
Mon Mar 31 19:02:30 GMT 2025
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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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Preferred Name | English | ||
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EPA PESTICIDE CODE |
129031
Created by
admin on Mon Mar 31 19:02:30 GMT 2025 , Edited by admin on Mon Mar 31 19:02:30 GMT 2025
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| Code System | Code | Type | Description | ||
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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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PRIMARY | Merck Index | ||
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NG7LE47J14
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91751
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