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Fenamiphos

IUPAC name ethyl-4-methylthio-m-tolyl isopropylphosphoramidate Molecular formula C13H22NO3PS Toxicity class USEPA I WHO la [Pg.138]

Figure 1 SRM chromatograms of (a) fenamiphos and metabolites and (b) imidacloprid and metabolites. IS refers to the stable labeled isotopes. The values below the names refer to the mass transitions, i.e., M -b 1 -> product ion for the metabolite... Figure 1 SRM chromatograms of (a) fenamiphos and metabolites and (b) imidacloprid and metabolites. IS refers to the stable labeled isotopes. The values below the names refer to the mass transitions, i.e., M -b 1 -> product ion for the metabolite...
Biodegradation can only take place if the sorbed pollutants can be rapidly released from the organoclay complex as is the case with naphthalene (Crocker et al. 1995) and the herbicide fenamiphos (Singh et al. 2003). [Pg.162]

Lamberti F, Greco N (1991) Effectiveness of soil solarization for control of plant parasitic nematodes. In DeVay JE, Stapleton JJ, Elmore CL (eds) Proceedings of the first international conference on soil solarization, Amman, Jordan, 19-25 February 1990. FAO Plant Protection and Production Paper No. 109, FAO, Rome, Italy, pp 167-172 Lamberti F, D Addabbo T, Greco P, Carella A, De Cosmis P (2000) Management of root-knot nematodes by combination of soil solarization and fenamiphos in southern Italy. Nematol Medit 28 31 15... [Pg.263]

CASRN 22224-92-6 molecular formula C13H22NO3PS FW 303.40 Soil. Oxidizes in soil to the fenamiphos sulfone and fenamiphos sulfoxide (Lee et al., 1986). Fenamiphos rapidly degraded in Arredondo soil to fenamiphos sulfone and the corresponding phenol. The half-life in this soil is 38-67 d (Ou and Rao, 1986). [Pg.1583]

Surface Water, in estuarine water, the half-life of fenamiphos was 1.80 d (Lacorte et al, 1995). Chemical/Physical. Emits toxic fumes of phosphorus, nitrogen, and sulfur oxides when heated to decomposition (Lewis, 1990). [Pg.1583]

Lee, C.-C., Green, R.E., andApt, W.J. Transformation and adsorption of fenamiphos, f. sulfoxide and f.sulfone in molokaisoil and simulated movement with irrigations, J. Contam. Hydro ., 1 211-225, 1986. [Pg.1685]

Ramesh, A. and Balasubramanian, M. Kinetics and hydrolysis of fenamiphos, fipronil, and trifluralin in aqueous buffer solutions, J. Agric. Food Chem., 47(8) 3367-3371, 1999. [Pg.1713]

Fenamiphos 303.4 49.3 700 Very soluble Very soluble Very soluble Very soluble 3.23-3.28... [Pg.721]

Mevinphos I, dimethoate, mevinphos II, dichlorvos, diazinon, paraoxon, azinphos-methyl, fenamiphos, parathion-methyl, malathion, fenitrothion, azinphos ethyl, fenthion, parathion-ethyl, coumaphos, phorate, phoxim, disulfoton, chlorpyriphos, ome-thoate, monocrotophos, vamidothion, bromophos ethyl, metoxichlor, DDT... [Pg.742]

Chlorpyriphos methyl, diazinon, disulfoton, fenamiphos, fenthion, isofenphos, malathion, methidathion, pyridafenthion, temephos... [Pg.744]

Water Trichlorfon, dichlorvos, mevinphos, demethon-S-methyl, dimethoate, oxydemeton-methyl, fenamiphos, fenthion ... [Pg.745]

Water Dimethoate, fenamiphos, bromophos ethyl, fenthion, coumaphos, fenchlorfos, chlorpyriphos, monocrotophos, mevinphos, fosphamidon, paraoxon, azinphos methyl, foxim, carbophenothion, bromophos methyl Carbamates, phenyl urea, anilides, nitrofenoles... [Pg.745]

See other pages where Fenamiphos is mentioned: [Pg.394]    [Pg.203]    [Pg.68]    [Pg.96]    [Pg.332]    [Pg.341]    [Pg.354]    [Pg.51]    [Pg.85]    [Pg.233]    [Pg.835]    [Pg.92]    [Pg.173]    [Pg.297]    [Pg.659]    [Pg.67]    [Pg.477]    [Pg.33]    [Pg.34]    [Pg.1250]    [Pg.1312]    [Pg.1375]    [Pg.1419]    [Pg.1583]    [Pg.70]    [Pg.68]    [Pg.96]    [Pg.358]    [Pg.374]    [Pg.375]    [Pg.375]    [Pg.394]    [Pg.720]    [Pg.725]    [Pg.744]   
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