Flazasulfuron | CAS#104040-78-0

MedKoo Cat#: 535722 | Name: Flazasulfuron

Description:

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

Flazasulfuron is a bioactive chemical.

Chemical Structure

Flazasulfuron

CAS#104040-78-0

Theoretical Analysis

MedKoo Cat#: 535722

Name: Flazasulfuron

CAS#: 104040-78-0

Chemical Formula: C13H12F3N5O5S

Exact Mass: 407.0511

Molecular Weight: 407.32

Elemental Analysis: C, 38.33; H, 2.97; F, 13.99; N, 17.19; O, 19.64; S, 7.87

Price and Availability

This product is currently not in stock but may be available through custom synthesis. To ensure cost efficiency, the minimum order quantity is 1 gram. The estimated lead time is 2 to 4 months, with pricing dependent on the complexity of the synthesis (typically high for intricate chemistries). Quotes for quantities below 1 gram will not be provided. To request a quote, please click the button below. Note: If this product becomes available in stock in the future, pricing will be listed accordingly.

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Related CAS #

No Data

Synonym

Flazasulfuron

IUPAC/Chemical Name

2-Pyridinesulfonamide, N-(((4,6-dimethoxy-2-pyrimidinyl)amino)carbonyl)-3-(trifluoromethyl)-

InChi Key

HWATZEJQIXKWQS-UHFFFAOYSA-N

InChi Code

InChI=1S/C13H12F3N5O5S/c1-25-8-6-9(26-2)19-11(18-8)20-12(22)21-27(23,24)10-7(13(14,15)16)4-3-5-17-10/h3-6H,1-2H3,(H2,18,19,20,21,22)

SMILES Code

O=S(C1=NC=CC=C1C(F)(F)F)(NC(NC2=NC(OC)=CC(OC)=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

2934.99.9001

More Info

Instruction

View handling instruction

Preparing Stock Solutions

The following data is based on the product molecular weight 407.32 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.

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: Mandl K, Cantelmo C, Gruber E, Faber F, Friedrich B, Zaller JG. Effects of Glyphosate-, Glufosinate- and Flazasulfuron-Based Herbicides on Soil Microorganisms in a Vineyard. Bull Environ Contam Toxicol. 2018 Nov;101(5):562-569. doi: 10.1007/s00128-018-2438-x. Epub 2018 Sep 18. PMID: 30229276; PMCID: PMC6223855. 2: Tahmasebi BK, Alcántara-de la Cruz R, Alcántara E, Torra J, Domínguez- Valenzuela JA, Cruz-Hipólito HE, Rojano-Delgado AM, De Prado R. Multiple Resistance Evolution in Bipyridylium-Resistant Epilobium ciliatum After Recurrent Selection. Front Plant Sci. 2018 May 28;9:695. doi: 10.3389/fpls.2018.00695. PMID: 29892306; PMCID: PMC5985439. 3: Couderchet M, Vernet G. Pigments as biomarkers of exposure to the vineyard herbicide flazasulfuron in freshwater algae. Ecotoxicol Environ Saf. 2003 Jul;55(3):271-7. doi: 10.1016/s0147-6513(02)00064-7. PMID: 12798760. 4: Magné C, Saladin G, Clément C. Transient effect of the herbicide flazasulfuron on carbohydrate physiology in Vitis vinifera L. Chemosphere. 2006 Jan;62(4):650-7. doi: 10.1016/j.chemosphere.2005.04.119. Epub 2005 Jun 28. PMID: 15987652. 5: Bertrand C, Witczak-Legrand A, Sabadie J, Cooper JF. Flazasulfuron: alcoholysis, chemical hydrolysis, and degradation on various minerals. J Agric Food Chem. 2003 Dec 17;51(26):7717-21. doi: 10.1021/jf0347970. PMID: 14664534. 6: Durigan-Marcel EB, Durigan JC, Gustavo M. Selectivity of the herbicide flazasulfuron applied after postemergence in sugarcane (Saccharum spp. L.) crop. J Environ Sci Health B. 2005;40(1):177-80. doi: 10.1081/pfc-200034303. PMID: 15656177. 7: Zaller JG, Cantelmo C, Santos GD, Muther S, Gruber E, Pallua P, Mandl K, Friedrich B, Hofstetter I, Schmuckenschlager B, Faber F. Herbicides in vineyards reduce grapevine root mycorrhization and alter soil microorganisms and the nutrient composition in grapevine roots, leaves, xylem sap and grape juice. Environ Sci Pollut Res Int. 2018 Aug;25(23):23215-23226. doi: 10.1007/s11356-018-2422-3. Epub 2018 Jun 3. PMID: 29862481; PMCID: PMC6096560. 8: Olette R, Couderchet M, Biagianti S, Eullaffroy P. Toxicity and removal of pesticides by selected aquatic plants. Chemosphere. 2008 Feb;70(8):1414-21. doi: 10.1016/j.chemosphere.2007.09.016. Epub 2007 Nov 5. PMID: 17980900. 9: Raeppel C, Fabritius M, Nief M, Appenzeller BM, Briand O, Tuduri L, Millet M. Analysis of airborne pesticides from different chemical classes adsorbed on Radiello® Tenax® passive tubes by thermal-desorption-GC/MS. Environ Sci Pollut Res Int. 2015 Feb;22(4):2726-34. doi: 10.1007/s11356-014-3534-z. Epub 2014 Sep 11. PMID: 25205153. 10: Botta F, Fauchon N, Blanchoud H, Chevreuil M, Guery B. Phyt'Eaux Cités: application and validation of a programme to reduce surface water contamination with urban pesticides. Chemosphere. 2012 Jan;86(2):166-76. doi: 10.1016/j.chemosphere.2011.10.005. Epub 2011 Nov 9. PMID: 22078267.