Saflufenacil

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

MedKoo CAT#: 558538

CAS#: 372137-35-4

Description: Saflufenacil is a uracil-based herbicide used to control annual broadleaf weeds in soybeans and corn.

Chemical Structure

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Saflufenacil
CAS# 372137-35-4
Instruction

Theoretical Analysis

MedKoo Cat#: 558538
Name: Saflufenacil
CAS#: 372137-35-4
Chemical Formula: C17H17ClF4N4O5S
Exact Mass: 500.05
Molecular Weight: 500.850
Elemental Analysis: C, 40.77; H, 3.42; Cl, 7.08; F, 15.17; N, 11.19; O, 15.97; S, 6.40

Price and Availability

This product is not in stock, which may be available by custom synthesis. For cost-effective reason, minimum order is 1g (price is usually high, lead time is 2~3 months, depending on the technical challenge). Quote less than 1g will not be provided. To request quote, please email to sales @medkoo.com or click below button.
Note: Price will be listed if it is available in the future.

Request quote for custom synthesis

Synonym: Saflufenacil; Kixor; Kixor Herbicide;

IUPAC/Chemical Name: 2-chloro-5-(3,6-dihydro-3-methyl-2,6-dioxo-4-(trifluoromethyl)-1(2H)-pyrimidinyl)-4-fluoro-N-((methyl(1-methylethyl)amino)sulfonyl)benzamide

InChi Key: GNHDVXLWBQYPJE-UHFFFAOYSA-N

InChi Code: InChI=1S/C17H17ClF4N4O5S/c1-8(2)25(4)32(30,31)23-15(28)9-5-12(11(19)6-10(9)18)26-14(27)7-13(17(20,21)22)24(3)16(26)29/h5-8H,1-4H3,(H,23,28)

SMILES Code: O=C(NS(=O)(N(C)C(C)C)=O)C1=CC(N(C(N(C)C(C(F)(F)F)=C2)=O)C2=O)=C(F)C=C1Cl

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:

Biological target:
In vitro activity:
In vivo activity:

Preparing Stock Solutions

The following data is based on the product molecular weight 500.85 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
Formulation protocol:
In vitro protocol:
In vivo protocol:

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1: Camargo ER, Senseman SA, Haney RL, Guice JB, McCauley GN. Soil residue analysis and degradation of saflufenacil as affected by moisture content and soil characteristics. Pest Manag Sci. 2013 Dec;69(12):1291-7. doi: 10.1002/ps.3494. Epub 2013 Mar 21. PubMed PMID: 23908059.

2: Lan M, Li S, Xu Z, Tian C, Yang M, Gui W, Zhu G. Simultaneous determination of saflufenacil and its two metabolites in soil samples by ultra-performance liquid chromatography with tandem mass spectrometry. J Sep Sci. 2014 Mar;37(6):658-64. doi: 10.1002/jssc.201301121. Epub 2014 Jan 29. PubMed PMID: 24382839.

3: Camargo ER, Senseman SA, McCauley GN, Bowe S, Harden J, Guice JB. Interaction between saflufenacil and imazethapyr in red rice (Oryza ssp.) and hemp sesbania (Sesbania exaltata) as affected by light intensity. Pest Manag Sci. 2012 Jul;68(7):1010-8. doi: 10.1002/ps.3260. Epub 2012 Feb 9. PubMed PMID: 22323402.

4: Ashigh J, Hall JC. Bases for interactions between saflufenacil and glyphosate in plants. J Agric Food Chem. 2010 Jun 23;58(12):7335-43. doi: 10.1021/jf100595a. PubMed PMID: 20481603.

5: Papiernik SK, Koskinen WC, Barber BL. Low sorption and fast dissipation of the herbicide saflufenacil in surface soils and subsoils of an eroded prairie landscape. J Agric Food Chem. 2012 Nov 7;60(44):10936-41. doi: 10.1021/jf303271p. Epub 2012 Oct 26. PubMed PMID: 23030723.

6: Zuo Y, Wu Q, Su SW, Niu CW, Xi Z, Yang GF. Synthesis, Herbicidal Activity, and QSAR of Novel N-Benzothiazolyl- pyrimidine-2,4-diones as Protoporphyrinogen Oxidase Inhibitors. J Agric Food Chem. 2016 Jan 27;64(3):552-62. doi: 10.1021/acs.jafc.5b05378. Epub 2016 Jan 14. PubMed PMID: 26728549.

7: Xie Y, Chi HW, Guan AY, Liu CL, Ma HJ, Cui DL. Design, synthesis, and herbicidal activity of novel substituted 3-(pyridin-2-yl)benzenesulfonamide derivatives. J Agric Food Chem. 2014 Dec 31;62(52):12491-6. doi: 10.1021/jf504018z. Epub 2014 Dec 19. PubMed PMID: 25437124.

8: Pandolfo CE, Presotto A, Carbonell FT, Ureta S, Poverene M, Cantamutto M. Transgenic glyphosate-resistant oilseed rape (Brassica napus) as an invasive weed in Argentina: detection, characterization, and control alternatives. Environ Sci Pollut Res Int. 2016 Dec;23(23):24081-24091. Epub 2016 Sep 16. PubMed PMID: 27638808.

9: Dayan FE, Owens DK, Duke SO. Rationale for a natural products approach to herbicide discovery. Pest Manag Sci. 2012 Apr;68(4):519-28. doi: 10.1002/ps.2332. Epub 2012 Jan 9. Review. PubMed PMID: 22232033.

10: Chahal PS, Ganie ZA, Jhala AJ. Overlapping Residual Herbicides for Control of Photosystem (PS) II- and 4-Hydroxyphenylpyruvate Dioxygenase (HPPD)-Inhibitor-Resistant Palmer amaranth (Amaranthus palmeri S. Watson) in Glyphosate-Resistant Maize. Front Plant Sci. 2018 Jan 9;8:2231. doi: 10.3389/fpls.2017.02231. eCollection 2017. PubMed PMID: 29375605; PubMed Central PMCID: PMC5767313.

11: Xie Y, Peng W, Ding F, Liu SJ, Ma HJ, Liu CL. Quantitative structure-activity relationship (QSAR) directed the discovery of 3-(pyridin-2-yl)benzenesulfonamide derivatives as novel herbicidal agents. Pest Manag Sci. 2018 Jan;74(1):189-199. doi: 10.1002/ps.4693. Epub 2017 Sep 11. PubMed PMID: 28762622.

12: Subedi M, Willenborg CJ, Vandenberg A. Influence of Harvest Aid Herbicides on Seed Germination, Seedling Vigor and Milling Quality Traits of Red Lentil (Lens culinaris L.). Front Plant Sci. 2017 Mar 14;8:311. doi: 10.3389/fpls.2017.00311. eCollection 2017. PubMed PMID: 28352275; PubMed Central PMCID: PMC5349153.

13: Casida JE. Why Prodrugs and Propesticides Succeed. Chem Res Toxicol. 2017 May 15;30(5):1117-1126. doi: 10.1021/acs.chemrestox.7b00030. Epub 2017 Apr 7. Review. PubMed PMID: 28334528.