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| | Flutriafol Basic information |
| | Flutriafol Chemical Properties |
| Melting point | 130° | | Boiling point | 506.5±60.0 °C(Predicted) | | density | 1.3015 (estimate) | | vapor pressure | 7.1 x l0-9 Pa (20 °C) | | Fp | 2 °C | | storage temp. | 0-6°C | | solubility | Chloroform (Slightly), DMSO (Slightly), Methanol (Slightly) | | pka | 11.60±0.29(Predicted) | | Water Solubility | 130 mg l-1 (pH 7,20 °C) | | form | neat | | color | White to Off-White | | Merck | 13,4240 | | BRN | 8155287 | | Stability: | Stable. Incompatible with strong oxidizing agents. | | InChIKey | JWUCHKBSVLQQCO-UHFFFAOYSA-N | | LogP | 2.290 | | CAS DataBase Reference | 76674-21-0(CAS DataBase Reference) | | NIST Chemistry Reference | Flutriafol(76674-21-0) | | EPA Substance Registry System | Flutriafol (76674-21-0) |
| Hazard Codes | Xn,F | | Risk Statements | 22-36-20/21/22-11 | | Safety Statements | 22-24/25-36-26 | | RIDADR | UN 1648 3/PG 2 | | WGK Germany | 3 | | RTECS | XZ4825000 | | HS Code | 29339900 | | Toxicity | LD50 male, female rats (mg/kg): 1140, 1480 orally; rats, rabbits: >1000, >2000 percutaneously (Skidmore) |
| | Flutriafol Usage And Synthesis |
| Chemical Properties | solid | | Uses | Agricultural fungicide. | | Uses | 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. | | Uses | 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. | | Definition | 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. | | Metabolic pathway | Flutriafol is stable to hydrolysis and to light and it is persistent in soils. In
crops, the metabolites identified were derivatives of triazole. | | Degradation | 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). |
| | Flutriafol Preparation Products And Raw materials |
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