prosulfuron

benzenesulfonamide, N-(((4-methoxy-6-methyl-1,3,5-triazin-2-yl)amino)carbonyl)-2-(3,3,3-trifluoropropyl)-

CAS: 94125-34-5 C15 H16 F3 N5 O4 S MW: 419.38452960

Identification

Nameprosulfuron
IUPAC1-(4-methoxy-6-methyl-1,3,5-triazin-2-yl)-3-[2-(3,3,3-trifluoropropyl)phenyl]sulfonylurea
CAS Number94125-34-5
FDA UNIING7LE47J14
Molecular FormulaC15 H16 F3 N5 O4 S
Molecular Weight419.38452960
MDL NumberMFCD01863141
Nikkaji NumberJ653.647F
Beilstein7800481

Regulatory

Physical Properties

Assay 95.00 to 100.00
Food Chemicals Codex Listed No
Melting Point 155.00 °C. @ 760.00 mm Hg
Flash Point 32.00 °F. TCC ( 0.00 °C. ) (est)
logP (o/w) 3.020 (est)
Soluble in water, 29 mg/L @ 25 °C (exp)

No sensory data available

Safety Information

Oral/Parenteral ToxicityNot determined
Dermal ToxicityNot determined
Inhalation ToxicityNot determined

GHS Classification

['GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)', 'GHS Label elements, including precautionary statements']

Safety in Use

Categoryherbicides / pesticides
Recommendation for prosulfuron usage levels up tonot for fragrance use.
Recommendation for prosulfuron flavor usage levels up tonot for flavor use.

BOC Sciences

Best of Chemicals Supplier

Quality supplier of research chemicals and biochemicals including inhibitors, building blocks, GMP Products, impurities and metabolites, APIs for Veterinary, Natural Compounds, ADCs, Stem Cell Molecul...

View All Website 1-631-485-4226 account@bocsci.com

Potential Uses

None Found

Natural Occurrence

not found in nature

Synonyms

benzenesulfonamide, N-(((4-methoxy-6-methyl-1,3,5-triazin-2-yl)amino)carbonyl)-2-(3,3,3-trifluoropropyl)- 1-(4- methoxy-6-methyl-1,3,5-triazin-2-yl)-3-[2-(3,3,3-trifluoropropyl)phenyl]sulfonylurea PubMed: Ionic-liquid-functionalized magnetic particles as an adsorbent for the magnetic SPE of sulfonylurea herbicides in environmental water samples. PubMed: Magnetic solid-phase extraction of sulfonylurea herbicides in environmental water samples by Fe3O4@dioctadecyl dimethyl ammonium chloride@silica magnetic particles. PubMed: Toxic effects of four sulphonylureas herbicides on soil microbial biomass. PubMed: Rapid determination of sixteen sulfonylurea herbicides in surface water by solid phase extraction cleanup and ultra-high-pressure liquid chromatography coupled with tandem mass spectrometry. 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. PubMed: No-tillage system applied to the sunflower (hybrid pioneer PR64E83) resistant to the tribenuron-methyl in the conditions from Romania. PubMed: Organic amendments from olive cake as a strategy to modify the degradation of sulfonylurea herbicides in soil. PubMed: Impact of an herbicide combination of bromoxynil and prosulfuron on soil microorganisms. PubMed: [Simultaneous determination of ten sulfonylurea herbicide residues in soybeans by high performance liquid chromatography]. PubMed: Crosstalk and differential response to abiotic and biotic stressors reflected at the transcriptional level of effector genes from secondary metabolism. PubMed: Hydrophilic and hydrophobic sorption of organic acids by variable charge soils: effect of chemical acidity and acidic functional group. PubMed: Factors controlling sorption of prosulfuron by variable-charge soils and model sorbents. PubMed: Soil transformation of prosulfuron. PubMed: Effects of soil pH and soil water content on prosulfuron dissipation. PubMed: Induction of cytochrome P450 genes by ethanol in maize.