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Formetanate

Fonofos Formaldehyde Formetanate.HCI Formic acid Furfural... [Pg.367]

Folpet heterocyclic nitrogen, indoledione Fomesafen amide, phenyl ether, sulfonamide Fonofos phosphoro organic, phosphoro dithioate Forchlorfenuron urea, pyridine Formetanate hydrochloride carbamate, amidine Formothion phosphoro organic, phosphoro dithioate, amide... [Pg.1008]

Dimethyl cyclopropane dicarboxylic acid anhydride procymidone Dimethyl formamide chlordimeform, formetanate... [Pg.1035]

Formamidine insecticides are all derivatives of formamidine (HN=CHNH,). This class comprises a new, small group of chemicals that exhibit insecticidal and miticidal properties. Three examples are chlordimeform, formetanate hydrochloride, and amitraz, shown as follows. [Pg.62]

SYNS CARZOL SP DICARZOL m-((piMETHYL-AiMINO)METHYLENE)AMINO)PHENYLMETHYL CARBAMATE,HYDR0CHL0RIDE 3-DIMETHYL-AMINOMETHYLENEIMINOPHENYL-N-METHYL-CARBAMATE, HYDROCHLORIDE ENT 27,566 EP-332 FORMETANATE HYDROCHLORIDE iMORTON EP332 NOR-AM EP 332 SCHERING 36056 SN 36056... [Pg.539]

Formamidines comprise a small group of promising insecticides. Chlordimeform, formetanate, and amitraz are examples of this group. These compounds are effective against most stages of mites and ticks. Thus they am classified as ovicides, insecticides, and acariddes. Formulations are emulsifi-able concentrates and water-soluble powders. [Pg.158]

Though subjectively defined, and often not intensively investigated with the necessary field and laboratory studies, the phenomenon of instability has been noted for TEPP resistance 22.), the organotin acaricides (24-26), propargite (fi.), dicofol (see below), and formetanate hydrochloride. Noteworthy contradictions regarding resistance stability exist. Welty et al. (22) found resistance to cyhexatin in Panonychus ulmi to be stable in two field... [Pg.79]

Formetanate Mineral, tap waters Microwave-assisted analyte hydrolysis UV-Vis 0.20 x 10-5 mol L 1 Flow injection system in-line waste treatment exploiting Ti02 addition and UV irradiation [430]... [Pg.329]

M.J. Escuriola, A. Morales-Rubio, M. de La Guardia, A clean analytical method for the spectrophotometric determination of formetanate incorporating an on-line microwave assisted hydrolysis step, Anal. Chim. Acta 390 (1999) 147. [Pg.441]

Dimethylaminomethyleneiminophenyl N-methylcarbamate (formetanate, 15) contains both amidine and carbamate groups (Wakerley and Weighton, 1969). The amidine moiety of the molecule is synthesised in the same way as described for chlorphenamidine, and the 3-dimethylaminomethyleneiminophenol obtained is carbamoylated with methyl isocyanate ... [Pg.245]

The acute oral of formetanate for rats is 24 mg/kg. It is particularly effective against the motile stages of spider mites. [Pg.245]

See other pages where Formetanate is mentioned: [Pg.420]    [Pg.291]    [Pg.223]    [Pg.223]    [Pg.52]    [Pg.481]    [Pg.67]    [Pg.420]    [Pg.696]    [Pg.291]    [Pg.361]    [Pg.59]    [Pg.83]    [Pg.83]    [Pg.1015]    [Pg.1016]    [Pg.1025]    [Pg.1039]    [Pg.1044]    [Pg.1064]    [Pg.1070]    [Pg.135]    [Pg.223]    [Pg.257]    [Pg.62]    [Pg.62]    [Pg.52]    [Pg.1698]    [Pg.52]    [Pg.579]    [Pg.579]    [Pg.69]    [Pg.69]    [Pg.69]    [Pg.171]    [Pg.78]    [Pg.553]    [Pg.384]   
See also in sourсe #XX -- [ Pg.83 ]



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Formetanate hydrochloride

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