MedKoo Cat#: 584147 | Name: Flurtamone
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Description:

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

Flurtamone is an agricultural chemical mainly used as an herbicide.

Chemical Structure

Flurtamone
Flurtamone
CAS#96525-23-4

Theoretical Analysis

MedKoo Cat#: 584147

Name: Flurtamone

CAS#: 96525-23-4

Chemical Formula: C18H14F3NO2

Exact Mass: 333.0977

Molecular Weight: 333.31

Elemental Analysis: C, 64.86; H, 4.23; F, 17.10; N, 4.20; O, 9.60

Price and Availability

Size Price Availability Quantity
100mg USD 450.00 Back order
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Related CAS #
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Synonym
Flurtamone; Benchmark; Fluortanone; BACCARA; RE 40885; RE-40885; RE40885; RE 40885;
IUPAC/Chemical Name
3(2H)-Furanone, 5-(methylamino)-2-phenyl-4-(3-(trifluoromethyl)phenyl)-
InChi Key
NYRMIJKDBAQCHC-UHFFFAOYSA-N
InChi Code
InChI=1S/C18H14F3NO2/c1-22-17-14(12-8-5-9-13(10-12)18(19,20)21)15(23)16(24-17)11-6-3-2-4-7-11/h2-10,16,22H,1H3
SMILES Code
O=C1C(C2=CC=CC=C2)OC(NC)=C1C3=CC=CC(C(F)(F)F)=C3
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
>2 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

Preparing Stock Solutions

The following data is based on the product molecular weight 333.31 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: Zhang Y, Zhou L, Li R, Li Y, Tan Y, Shi H, Wang M. Comprehensive Assessment of Enantioselective Bioactivity, Toxicity, and Dissipation in Soil of the Chiral Herbicide Flurtamone. J Agric Food Chem. 2023 Mar 29;71(12):4810-4816. doi: 10.1021/acs.jafc.3c00223. Epub 2023 Mar 15. PMID: 36919602. 2: Hillebrands L, Lamshoeft M, Lagojda A, Stork A, Kayser O. In vitro metabolism of tebuconazole, flurtamone, fenhexamid, metalaxyl-M and spirodiclofen in Cannabis sativa L. (hemp) callus cultures. Pest Manag Sci. 2021 Dec;77(12):5356-5366. doi: 10.1002/ps.6575. Epub 2021 Aug 6. PMID: 34309997; PMCID: PMC9292707. 3: Hillebrands L, Lamshoeft M, Lagojda A, Stork A, Kayser O. Evaluation of Callus Cultures to Elucidate the Metabolism of Tebuconazole, Flurtamone, Fenhexamid, and Metalaxyl-M in Brassica napus L., Glycine max (L.) Merr., Zea mays L., and Triticum aestivum L. J Agric Food Chem. 2020 Nov 20. doi: 10.1021/acs.jafc.0c05277. Epub ahead of print. PMID: 33215910. 4: Sandmann G, Ward CE, Lo WC, Nagy JO, Böger P. Bleaching herbicide flurtamone interferes with phytoene desaturase. Plant Physiol. 1990 Oct;94(2):476-8. doi: 10.1104/pp.94.2.476. PMID: 16667736; PMCID: PMC1077256. 5: European Food Safety Authority (EFSA); Arena M, Auteri D, Barmaz S, Bellisai G, Brancato A, Brocca D, Bura L, Byers H, Chiusolo A, Court Marques D, Crivellente F, De Lentdecker C, De Maglie M, Egsmose M, Erdos Z, Fait G, Ferreira L, Goumenou M, Greco L, Ippolito A, Istace F, Jarrah S, Kardassi D, Leuschner R, Lythgo C, Magrans JO, Medina P, Miron I, Molnar T, Nougadere A, Padovani L, Parra Morte JM, Pedersen R, Reich H, Sacchi A, Santos M, Serafimova R, Sharp R, Stanek A, Streissl F, Sturma J, Szentes C, Tarazona J, Terron A, Theobald A, Vagenende B, Verani A, Villamar-Bouza L. Updated peer review of the pesticide risk assessment of the active substance flurtamone. EFSA J. 2017 Sep 8;15(9):e04976. doi: 10.2903/j.efsa.2017.4976. PMID: 32625641; PMCID: PMC7009922. 6: Dücker R, Zöllner P, Parcharidou E, Ries S, Lorentz L, Beffa R. Enhanced metabolism causes reduced flufenacet sensitivity in black-grass (Alopecurus myosuroides Huds.) field populations. Pest Manag Sci. 2019 Nov;75(11):2996-3004. doi: 10.1002/ps.5414. Epub 2019 Apr 29. PMID: 30891919. 7: Linden H, Misawa N, Chamovitz D, Pecker I, Hirschberg J, Sandmann G. Functional complementation in Escherichia coli of different phytoene desaturase genes and analysis of accumulated carotenes. Z Naturforsch C J Biosci. 1991 Nov- Dec;46(11-12):1045-51. doi: 10.1515/znc-1991-11-1219. PMID: 1817513. 8: Suarez JV, Banks S, Thomas PG, Day A. A new F131V mutation in Chlamydomonas phytoene desaturase locates a cluster of norflurazon resistance mutations near the FAD-binding site in 3D protein models. PLoS One. 2014 Jun 17;9(6):e99894. doi: 10.1371/journal.pone.0099894. PMID: 24936791; PMCID: PMC4061028. 9: Scheurer M, Nödler K, Freeling F, Janda J, Happel O, Riegel M, Müller U, Storck FR, Fleig M, Lange FT, Brunsch A, Brauch HJ. Small, mobile, persistent: Trifluoroacetate in the water cycle - Overlooked sources, pathways, and consequences for drinking water supply. Water Res. 2017 Dec 1;126:460-471. doi: 10.1016/j.watres.2017.09.045. Epub 2017 Sep 26. PMID: 28992593. 10: Galán-Jiménez MC, Gómez-Pantoja E, Morillo E, Undabeytia T. Solubilization of herbicides by single and mixed commercial surfactants. Sci Total Environ. 2015 Dec 15;538:262-9. doi: 10.1016/j.scitotenv.2015.08.008. Epub 2015 Aug 24. PMID: 26311582. 11: Desmet EM, Bulcke R, Maeghe L. Field experiences with recent ALS-inhibitors on herbicide resistant blackgrass (Alopecurus myosuroides Huds.). Commun Agric Appl Biol Sci. 2004;69(3):83-9. PMID: 15759398. 12: Galán-Jiménez Mdel C, Mishael YG, Nir S, Morillo E, Undabeytia T. Factors affecting the design of slow release formulations of herbicides based on clay- surfactant systems. A methodological approach. PLoS One. 2013;8(3):e59060. doi: 10.1371/journal.pone.0059060. Epub 2013 Mar 19. PMID: 23527087; PMCID: PMC3602540.