MedKoo Biosciences, Inc.
Tel:   +1-919-636-5577    Fax:   +1-919-980-4831    Email:   sales@medkoo.com
Search
Login Register
Search
MedKoo Cat#: 461694 | Name: Triflusulfuron-methyl
Featured

Description:

WARNING: This product is for research use only, not for human or veterinary use.

Triflusulfuron-methyl is a triazinylsulfonylurea herbicide.

Chemical Structure

Triflusulfuron-methyl
Triflusulfuron-methyl
CAS#126535-15-7

Theoretical Analysis

MedKoo Cat#: 461694

Name: Triflusulfuron-methyl

CAS#: 126535-15-7

Chemical Formula: C17H19F3N6O6S

Exact Mass: 492.1039

Molecular Weight: 492.43

Elemental Analysis: C, 41.47; H, 3.89; F, 11.57; N, 17.07; O, 19.49; S, 6.51

Price and Availability

Size Price Availability Quantity
100mg USD 270.00
Bulk Inquiry
Buy Now
Add to Cart
Related CAS #
No Data
Synonym
Triflusulfuron-methyl; Upbeet; DPX 66037; DPX-66037; DPX66037;
IUPAC/Chemical Name
methyl 2-(N-((4-(dimethylamino)-6-(2,2,2-trifluoroethoxy)-1,3,5-triazin-2-yl)carbamoyl)sulfamoyl)-3-methylbenzoate
InChi Key
IMEVJVISCHQJRM-UHFFFAOYSA-N
InChi Code
InChI=1S/C17H19F3N6O6S/c1-9-6-5-7-10(12(27)31-4)11(9)33(29,30)25-15(28)22-13-21-14(26(2)3)24-16(23-13)32-8-17(18,19)20/h5-7H,8H2,1-4H3,(H2,21,22,23,24,25,28)
SMILES Code
O=C(OC)C1=CC=CC(C)=C1S(=O)(NC(NC2=NC(N(C)C)=NC(OCC(F)(F)F)=N2)=O)=O
Appearance
Solid powder
Purity
>98% (or refer to the Certificate of Analysis)
Shipping Condition
Shipped under ambient temperature as non-hazardous chemical. This product is stable enough for a few weeks during ordinary shipping and time spent in Customs.
Storage Condition
Dry, dark and at 0 - 4 C for short term (days to weeks) or -20 C for long term (months to years).
Solubility
Soluble in DMSO
Shelf Life
>3 years if stored properly
Drug Formulation
This drug may be formulated in DMSO
Stock Solution Storage
0 - 4 C for short term (days to weeks), or -20 C for long term (months).
HS Tariff Code
2934.99.03.00
More Info

Preparing Stock Solutions

The following data is based on the product molecular weight 492.43 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.

Recalculate based on batch purity %
Concentration / Solvent Volume / Mass 1 mg 5 mg 10 mg
1 mM 1.15 mL 5.76 mL 11.51 mL
5 mM 0.23 mL 1.15 mL 2.3 mL
10 mM 0.12 mL 0.58 mL 1.15 mL
50 mM 0.02 mL 0.12 mL 0.23 mL
1: Rodríguez-Palma CE, Herráez-Hernández R, Campíns-Falcó P. A modified micro- solid phase extraction device for in-port elution and injection into portable liquid chromatography: A proof-of-concept study. J Chromatogr A. 2023 Aug 30;1705:464216. doi: 10.1016/j.chroma.2023.464216. Epub 2023 Jul 15. PMID: 37480726. 2: European Food Safety Authority (EFSA); Alvarez F, Arena M, Auteri D, Binaglia M, Castoldi AF, Chiusolo A, Colagiorgi A, Colas M, Crivellente F, De Lentdecker C, Egsmose M, Fait G, Ferilli F, Gouliarmou V, Nogareda LH, Ippolito A, Istace F, Jarrah S, Kardassi D, Kienzler A, Lanzoni A, Lava R, Linguadoca A, Lythgo C, Magrans O, Mangas I, Miron I, Molnar T, Padovani L, Parra Morte JM, Serafimova R, Sharp R, Szentes C, Terron A, Theobald A, Tiramani M, Villamar-Bouza L. Peer review of the pesticide risk assessment of the active substance triflusulfuron- methyl. EFSA J. 2022 May 18;20(5):e07303. doi: 10.2903/j.efsa.2022.7303. PMID: 35600269; PMCID: PMC9115678. 3: Luo R, Shen B, Xiang P, Liu W. Determination of twenty herbicides in blood by ultrapressure liquid chromatography-tandem mass spectrometry. Forensic Sci Int. 2021 Oct;327:110910. doi: 10.1016/j.forsciint.2021.110910. Epub 2021 Jul 20. PMID: 34425306. 4: Yu CY, Lian JL, Gong Q, Ren LS, Huang Z, Xu AX, Dong JG. Sublethal application of various sulfonylurea and imidazolinone herbicides favors outcrossing and hybrid seed production in oilseed rape. BMC Plant Biol. 2020 Feb 11;20(1):69. doi: 10.1186/s12870-020-2278-9. PMID: 32046649; PMCID: PMC7014721. 5: Chen L, Wu J, Huang X. Multiple monolithic fibers modified with a molecularly imprinted polymer for solid phase microextraction of sulfonylurea herbicides based on boron-nitrogen interaction. Mikrochim Acta. 2019 Jun 25;186(7):470. doi: 10.1007/s00604-019-3610-7. PMID: 31240479. 6: Bragina IV, Fedorova NE, Volkova VN, Egorchenkova OE, Mukhina LP, Larkina MV. [The method of multicomponent determination of herbicides of various chemical classes in water]. Gig Sanit. 2016;95(11):1099-104. Russian. PMID: 29446274. 7: Gure A, Lara FJ, García-Campaña AM, Megersa N, del Olmo-Iruela M. Vortex- assisted ionic liquid dispersive liquid-liquid microextraction for the determination of sulfonylurea herbicides in wine samples by capillary high- performance liquid chromatography. Food Chem. 2015 Mar 1;170:348-53. doi: 10.1016/j.foodchem.2014.08.065. Epub 2014 Aug 23. PMID: 25306356. 8: Rieke S, Koehn S, Hirsch-Ernst K, Pfeil R, Kneuer C, Marx-Stoelting P. Combination effects of (tri)azole fungicides on hormone production and xenobiotic metabolism in a human placental cell line. Int J Environ Res Public Health. 2014 Sep 17;11(9):9660-79. doi: 10.3390/ijerph110909660. PMID: 25233012; PMCID: PMC4199042. 9: He Z, Liu D, Zhou Z, Wang P. Ionic-liquid-functionalized magnetic particles as an adsorbent for the magnetic SPE of sulfonylurea herbicides in environmental water samples. J Sep Sci. 2013 Oct;36(19):3226-33. doi: 10.1002/jssc.201300390. Epub 2013 Aug 27. PMID: 23894051. 10: Nanita SC, Padivitage NL. Ammonium chloride salting out extraction/cleanup for trace-level quantitative analysis in food and biological matrices by flow injection tandem mass spectrometry. Anal Chim Acta. 2013 Mar 20;768:1-11. doi: 10.1016/j.aca.2013.01.011. Epub 2013 Jan 16. PMID: 23473245. 11: De Cauwer B, Devos R, Claerhout S, Bulcke R, Reheul D. Seed germination, seedling emergence, seed persistence and triflusulfuron-methyl sensitivity in Galinsoga parviflora and G. quadriradiata. Commun Agric Appl Biol Sci. 2013;78(3):681-91. PMID: 25151846. 12: He Z, Liu D, Li R, Zhou Z, Wang P. Magnetic solid-phase extraction of sulfonylurea herbicides in environmental water samples by Fe3O4@dioctadecyl dimethyl ammonium chloride@silica magnetic particles. Anal Chim Acta. 2012 Oct 17;747:29-35. doi: 10.1016/j.aca.2012.08.015. Epub 2012 Aug 27. PMID: 22986132. 13: Mereiter K. A 1:1 co-crystal of the herbicide triflusulfuron-methyl and its degradation product triazine amine. Acta Crystallogr Sect E Struct Rep Online. 2011 Sep 1;67(Pt 9):o2321-2. doi: 10.1107/S1600536811031631. Epub 2011 Aug 11. PMID: 22058947; PMCID: PMC3200658. 14: Nanita SC, Stry JJ, Pentz AM, McClory JP, May JH. Fast extraction and dilution flow injection mass spectrometry method for quantitative chemical residue screening in food. J Agric Food Chem. 2011 Jul 27;59(14):7557-68. doi: 10.1021/jf104237y. Epub 2011 Mar 9. PMID: 21388127. 15: Gigliotti G, Onofri A, Pannacci E, Businelli D, Trevisan M. Influence of dissolved organic matter from waste material on the phytotoxicity and environmental fate of triflusulfuron methyl. Environ Sci Technol. 2005 Oct 1;39(19):7446-51. doi: 10.1021/es048234w. PMID: 16245814. 16: Cougnaud A, Faur C, Le Cloirec P. Removal of pesticides from aqueous solution: Quantitative relationship between activated carbon characteristics and adsorption properties. Environ Technol. 2005 Aug;26(8):857-66. doi: 10.1080/09593332608618497. PMID: 16128384. 17: Chafik N, Mansour M, Elamrani B, Schramm KW, Kettrup A, Elamrani MK. Application of coupled liquid chromatography-mass spectrometry in photolysis studies of the herbicide triflusulfuron-methyl. Pest Manag Sci. 2001 Jun;57(6):527-30. doi: 10.1002/ps.314. PMID: 11407029. 18: Vega D, Cambon JP, Bastide J. Triflusulfuron-methyl dissipation in water and soil. J Agric Food Chem. 2000 Aug;48(8):3733-7. doi: 10.1021/jf9910943. PMID: 10956179.

View History

MRS1754

MRS1754

Featured