ENSIKLOPEDIA Cari Tekan Enter untuk memulai pencarian cepat. Kembali ke Ensiklopedia Arsip Wikipedia Indonesia Sulfometuron methyl Sulfometuron methyl Sulfometuron methyl Names Preferred IUPAC name Methyl 2-{[(4,6-dimethylpyrimidin-2-yl)carbamoyl]sulfamoyl}benzoate Identifiers CAS Number 74222-97-2 Y 3D model (JSmol) Interactive image ChEBI CHEBI:9348 ChEMBL ChEMBL513261 ChemSpider 47881 ECHA InfoCard 100.070.688 EC Number 277-780-6 KEGG C10955 PubChem CID 52997 UNII JLY5D60J1A Y CompTox Dashboard (EPA) DTXSID0034936 InChI InChI=1S/C15H16N4O5S/c1-9-8-10(2)17-14(16-9)18-15(21)19-25(22,23)12-7-5-4-6-11(12)13(20)24-3/h4-8H,1-3H3,(H2,16,17,18,19,21)Key: ZDXMLEQEMNLCQG-UHFFFAOYSA-N SMILES CC1=CC(=NC(=N1)NC(=O)NS(=O)(=O)C2=CC=CC=C2C(=O)OC)C Properties Chemical formula C15H16N4O5S Molar mass 364.38 g·mol−1 Appearance White solid Density 1.48 g/cm3 Melting point 202 °C (396 °F; 475 K) Solubility in water 244 mg/L Acidity (pKa) 5.2 Hazards GHS labelling: Pictograms Signal word Warning Hazard statements H319, H332, H410 Precautionary statements P261, P264+P265, P271, P273, P280, P304+P340, P305+P351+P338, P317, P337+P317, P391, P501 Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references Chemical compound Sulfometuron methyl is an organic compound used as an herbicide.[1] It is classed as a sulfonylurea. It functions via the inhibition of the enzyme acetolactate synthase, which catalyzes the first step in biosynthesis of the branched-chain amino acids valine, leucine, and isoleucine.[2] Sulfometuron methyl's HRAC classification is Group B (global, Aus), Group 2 (numeric), as it inhibits acetohydroxyacid synthase.[3] References ↑ "Sulfometuron-methyl". Extension Toxicology Network. Retrieved 10 February 2016. ↑ LaRossa, Robert; Schloss, John (1984). "The Sulfonylurea Herbicide Sulfometuron Methyl Is an Extremely Potent and Selective Inhibitor of Acetolactate Synthase in Salmonella typhimurium". Journal of Biological Chemistry. 259 (14): 8753–8757. doi:10.1016/S0021-9258(17)47217-6. PMID 6378902. ↑ "Classification of Herbicides According to Site of Action". Retrieved 19 July 2025. vtePest control: herbicidesAnilides/anilines acetochlor alachlor asulam benfluralin butachlor diethatyl diflufenican dimethenamid flamprop metazachlor metolachlor oryzalin pendimethalin pretilachlor propachlor propanil trifluralin Aromatic acids aminopyralid chloramben clopyralid dicamba picloram pyrithiobac quinclorac quinmerac Arsenicals cacodylic acid copper arsenate DSMA MSMA HPPD inhbitors flurochloridone isoxaflutole leptospermone mesotrione nitisinone sethoxydim sulcotrione Nitriles DCBN bromoxynil ioxynil Organophosphorus bensulide bialaphos ethephon fosamine glufosinate glyphosate piperophos PhenoxyAuxins 2,4-D 2,4-DB dichlorprop fenoprop MCPA MCPB mecoprop 2,4,5-T ACCase inhibitorsFOP herbicides chlorazifop cyhalofop diclofop fenoxaprop fluazifop haloxyfop quizalofop DIM herbicides alloxydim clethodim cycloxydim butroxydim sethoxydim Protox inhibitorsNitrophenyl ethers acifluorfen aclonifen bifenox fluorodifen fomesafen lactofen nitrofen oxyfluorfen Pyrimidinediones butafenacil saflufenacil Triazolinones carfentrazone sulfentrazone Pyridines dithiopyr fluroxypyr imazapyr thiazopyr triclopyr QuaternaryPhotosystem I inhibitors cyperquat diquat paraquat Thiocarbamates Benthiocarb Butylate S-Ethyl dipropylthiocarbamate prosulfocarb Triazinescellulose biosynthesis inhibitors indaziflam Photosystem II inhibitors ametryn atrazine cyanazine hexazinone metamitron metribuzin prometon prometryn propazine simazine simetryn terbuthylazine terbutryn UreasPhotosystem II inhibitors chlortoluron DCMU difenoxuron isoproturon linuron monuron monolinuron tebuthiuron ALS inhibitors chlorsulfuron flazasulfuron metsulfuron-methyl sulfometuron methyl tribenuron Others 3-AT aminocyclopyrachlor Bentazon clomazone dinoseb dinoterb juglone methazole metam sodium pyribenzoxim
