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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
Structure of PROSULFURON

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)

HIDE SMILES / InChI

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

PubMed

TitleDatePubMed
Soil transformation of prosulfuron.
2003 Jun 4
Factors controlling sorption of prosulfuron by variable-charge soils and model sorbents.
2004 Jul-Aug
[Simultaneous determination of ten sulfonylurea herbicide residues in soybeans by high performance liquid chromatography].
2004 Nov
Hydrophilic and hydrophobic sorption of organic acids by variable charge soils: effect of chemical acidity and acidic functional group.
2004 Oct 15
No-tillage system applied to the sunflower (hybrid pioneer PR64E83) resistant to the tribenuron-methyl in the conditions from Romania.
2007
A composite transcriptional signature differentiates responses towards closely related herbicides in Arabidopsis thaliana and Brassica napus.
2010 Mar
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

Sample Use Guides

Rat LD50 4360 mg/kg body weight
Route of Administration: Oral
Substance Class Chemical
Created
by admin
on Fri Dec 15 18:06:36 GMT 2023
Edited
by admin
on Fri Dec 15 18:06:36 GMT 2023
Record UNII
NG7LE47J14
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
PROSULFURON
ISO   MI  
Common Name English
PEAK
Brand Name English
N-(((4-METHOXY-6-METHYL-1,3,5-TRIAZIN-2-YL)AMINO)CARBONYL)-2-(3,3,3-TRIFLUOROPROPYL)BENZENESULFONAMIDE
Systematic Name English
1-(4-METHOXY-6-METHYL-1,3,5-TRIAZIN-2-YL)-3-(2-(3,3,3-TRIFLUOROPROPYL)PHENYLSULFONYL)UREA
Systematic Name English
CGA-152005
Code English
PROSULFURON [MI]
Common Name English
PROSULFURON [ISO]
Common Name English
Classification Tree Code System Code
EPA PESTICIDE CODE 129031
Created by admin on Fri Dec 15 18:06:36 GMT 2023 , Edited by admin on Fri Dec 15 18:06:36 GMT 2023
Code System Code Type Description
CAS
94125-34-5
Created by admin on Fri Dec 15 18:06:36 GMT 2023 , Edited by admin on Fri Dec 15 18:06:36 GMT 2023
PRIMARY
ALANWOOD
prosulfuron
Created by admin on Fri Dec 15 18:06:36 GMT 2023 , Edited by admin on Fri Dec 15 18:06:36 GMT 2023
PRIMARY
EPA CompTox
DTXSID9034868
Created by admin on Fri Dec 15 18:06:36 GMT 2023 , Edited by admin on Fri Dec 15 18:06:36 GMT 2023
PRIMARY
MERCK INDEX
m9262
Created by admin on Fri Dec 15 18:06:36 GMT 2023 , Edited by admin on Fri Dec 15 18:06:36 GMT 2023
PRIMARY Merck Index
FDA UNII
NG7LE47J14
Created by admin on Fri Dec 15 18:06:36 GMT 2023 , Edited by admin on Fri Dec 15 18:06:36 GMT 2023
PRIMARY
PUBCHEM
91751
Created by admin on Fri Dec 15 18:06:36 GMT 2023 , Edited by admin on Fri Dec 15 18:06:36 GMT 2023
PRIMARY