IUPAC/Chemical Name
DL-Alanine, N-benzoyl-N-(3-chloro-4-fluorophenyl)-
InChi Key
YQVMVCCFZCMYQB-UHFFFAOYSA-N
InChi Code
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)
SMILES Code
CC(C(O)=O)N(C(C1=CC=CC=C1)=O)C2=CC=C(F)C(Cl)=C2
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
Preparing Stock Solutions
The following data is based on the
product
molecular weight
321.73
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: 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.
