Flamprop

For research use only. Not for therapeutic Use.

  • CAT Number: I027525
  • CAS Number: 58667-63-3
  • Molecular Formula: C16H13ClFNO3
  • Molecular Weight: 321.73
  • Purity: 98%
Inquiry Now

Flamprop (Cat.No:I027525) is a herbicide widely used in agricultural practices to control the growth of weeds and grasses. It belongs to the chemical class of aryloxyphenoxypropionates and acts by inhibiting the enzyme acetyl-CoA carboxylase, crucial for lipid synthesis in plants. Flamprop offers selective and effective weed control in various crops.


Catalog Number I027525
CAS Number 58667-63-3
Synonyms

Flamprop

Molecular Formula C16H13ClFNO3
Purity 98%
Solubility Soluble in DMSO
Appearance Solid powder
Storage Dry, dark and at 0 - 4℃ for short term (days to weeks) or -20℃ for long term (months to years).
IUPAC Name DL-Alanine, N-benzoyl-N-(3-chloro-4-fluorophenyl)-
InChI InChI=1S/C16H13ClFNO3/c1-10(16(21)22)19(12-7-8-14(18)13(17)9-12)15(20)11-5-3-2-4-6-11/h2-10H,1H3,(H,21,22)
InChIKey YQVMVCCFZCMYQB-UHFFFAOYSA-N
SMILES CC(C(O)=O)N(C(C1=CC=CC=C1)=O)C2=CC=C(F)C(Cl)=C2
Reference

1: Tresch S, Niggeweg R, Grossmann K. The herbicide flamprop-M-methyl has a new antimicrotubule mechanism of action. Pest Manag Sci. 2008 Nov;64(11):1195-203. doi: 10.1002/ps.1618. PMID: 18551723.
2: Hutson DH, Crayford JV, Hoadley EC. The fate of the herbicide flamprop- isopropyl (barnon) in rats and dogs. Xenobiotica. 1977 May;7(5):279-300. doi: 10.3109/00498257709035786. PMID: 899038.
3: Brain KR, James V. Metabolism of [(14)C]Flamprop-isopropyl in suspension cultures from Medicago sativa and Phaseolus sp. Plant Cell Rep. 1982 Jun;1(4):172-5. doi: 10.1007/BF00269191. PMID: 24259137.
4: Jia W, Chu X, Zhang F. Multiresidue pesticide analysis in nutraceuticals from green tea extracts by comprehensive two-dimensional gas chromatography with time-of-flight mass spectrometry. J Chromatogr A. 2015 May 22;1395:160-6. doi: 10.1016/j.chroma.2015.03.071. Epub 2015 Apr 1. PMID: 25865796.
5: Hakme E, Lozano A, Gómez-Ramos MM, Hernando MD, Fernández-Alba AR. Non-target evaluation of contaminants in honey bees and pollen samples by gas chromatography time-of-flight mass spectrometry. Chemosphere. 2017 Oct;184:1310-1319. doi: 10.1016/j.chemosphere.2017.06.089. Epub 2017 Jun 20. PMID: 28679151.
6: Zertal A, Jacquet M, Lavédrine B, Sehili T. Photodegradation of chlorinated pesticides dispersed on sand. Chemosphere. 2005 Mar;58(10):1431-7. doi: 10.1016/j.chemosphere.2004.09.085. PMID: 15686762.
7: Fenni M, Shakir AN, Maillet J. Comparative efficacy of five herbicides on winter cereal weeds in semi-arid region of Algeria. Meded Rijksuniv Gent Fak Landbouwkd Toegep Biol Wet. 2001;66(2b):791-5. PMID: 12425104.
8: Díez C, Barrado E. Soil-dissipation kinetics of twelve herbicides used on a rain-fed barley crop in Spain. Anal Bioanal Chem. 2010 Jun;397(4):1617-26. doi: 10.1007/s00216-010-3671-2. Epub 2010 Apr 25. PMID: 20419492.
9: André C, Berthelot A, Thomassin M, Guillaume YC. Enantioselective aptameric molecular recognition material: Design of a novel chiral stationary phase for enantioseparation of a series of chiral herbicides by capillary electrochromatography. Electrophoresis. 2006 Aug;27(16):3254-62. doi: 10.1002/elps.200500070. PMID: 16865666.
10: Bedford CT, Crayford JV, Hutson DH, Wiggins DE. An example of the oxidative de-esterification of an isopropyl ester. Its role in the metabolism of the herbicide flampropisopropyl. Xenobiotica. 1978 Jun;8(6):383-95. doi: 10.3109/00498257809070022. PMID: 676346.
11: Desiderio C, Polcaro CM, Fanali S. Stereoselective analysis of herbicides by capillary electrophoresis using sulfobutyl ether beta-cyclodextrin as chiral selector. Electrophoresis. 1997 Feb;18(2):227-34. doi: 10.1002/elps.1150180209. PMID: 9080130.

Request a Quote