Little information is available for the specific isomer but is for the isomeric mixture. Flutriafol is a commonly used curative and preventative fungicide. It is moderately soluble in water, tends to be persistent in soil systems and is often stable in aquatic systems. It is moderately mobile and so may leach to groundwaters under certain conditions. It is moderately toxic to most biodiversity including honeybees and earthworms. It may be a development and/or reproduction toxin.
Little data is available for the isomer but is available for the isomeric mixture. Flutriafol is a commonly used curative and preventative fungicide. It is moderately soluble in water, tends to be persistent in soil systems and is often stable in aquatic systems. It is moderately mobile and so may leach to groundwaters under certain conditions. It is moderately toxic to most biodiversity including honeybees and earthworms. It may be a development and/or reproduction toxin,
Flutriafol is a commonly used curative and preventative fungicide. It is moderately soluble in water, tends to be persistent in soil systems and is often stable in aquatic systems. It is moderately mobile and so may leach to groundwaters under certain conditions. It is moderately toxic to most biodiversity including honeybees and earthworms. It may be a development and/or reproduction toxin.
Flutriafol is used to control a wide variety of leaf and ear diseases
in cereals. It is also used in seed treatment formulations to control the
major soil-borne and seed-borne diseases of cereals.
Flutriafol is a systemic fungicide of the triazole class. Flutriafol has broad spectrum fungicidal activity and is used to control effectively cereal powdery mildew, cloud disease, leaf spot disease a
nd rust disease.
ChEBI: 1-(2-fluorophenyl)-1-(4-fluorophenyl)-2-(1H-1,2,4-triazol-1-yl)ethanol is a tertiary alcohol that is ethanol in which one of the hydrogens at position 1 is replaced by an p-fluorophenyl group, the other hydrogen at position 1 is replaced by a p-fluorophenyl group, and one of the hydrogens at position 2 is replaced by a 1H-1,2,4-triazol-1-yl group. It is a member of triazoles, a tertiary alcohol and a member of monofluorobenzenes.
Broad-spectrum, systemic, contact action with eradicant and protective properties. Sterol biosynthesis inhibitor.
Broad-spectrum, systemic, contact action with eradicant and protective properties. Sterol biosynthesis inhibitor.
Broad-spectrum, systemic, contact action with eradicant and protective properties. Sterol biosynthesis inhibitor.
Anhydrous potassium fluoride was reacted with 2,3,4,5-tetrachloronitrobenzene in anhydrous dimethylformamide at 140C for 15 hours to obtain 2,4-difluoro-3,5-dichloronitrobenzene, and then the reaction was carried out in acetic acid at 95-100C for 8 hours with iron powder reduction to obtain 2,4-difluoro-3,5-dichlorobenzenamine. -2,6-difluorobenzamide reacted with oxalyl chloride in toluene at reflux for 5 hours to obtain 2,6-difluorobenzoyl isocyanate, and then reacted with the above mentioned 2,4-difluoro-3,5-dichloroaniline in toluene at room temperature for 15 hours, and the white solid powder obtained was powdery mildew.
Flutriafol is stable to hydrolysis and to light and it is persistent in soils. In
crops, the metabolites identified were derivatives of triazole.
Flutriafol, 1, is stable to hydrolysis at pH 5,7 and 9 in water at 50 °C over
a period of 30 days in the dark.
[14C-friazole]Flutriafoaln d [14C-carbinol]flutriafol were applied at a rate
equivalent to 94 g ai ha-1 to samples of dry sandy loam soil distributed as
a thin layer on 10 cm diameter glass plates. Samples were exposed to
natural sunlight for 30 days or to alternating periods of 'black light' and
darkness for 7 days. Recovery was 60-47% of applied radioactivity after
7 days artificial illumination and 74-85% after exposure to natural sunlight.
All degradation products accounted for ＜5 %of the total applied
radioactivity (PSD, 1996).
