Flutriafol Basic information
Product Name: Flutriafol
Synonyms: 1-(2-Fluorophenyl)-1-(4-fluorophenyl)-2-(1H-1,2,4-triazol-1-yl)ethanol;1-(2-fluorophenyl)-1-(4-fluorophenyl)-2-(1,2,4-triazol-1-yl)ethanol;Flutriafol 100mg [76674-21-0];(R)-1-(2-fluorophenyl)-1-(4-fluorophenyl)-2-(1H-1,2,4-triazol-1-yl)ethanol;PP 450-5;Flutriafol 0.1;Flutriafol TC (95%);VINCIT
CAS: 76674-21-0
MF: C16H13F2N3O
MW: 301.29
EINECS:
Product Categories: Agriculture;Alpha sort;ConazolesPesticides&Metabolites;E-GAlphabetic;F;FA - FL;Fungicides;Pesticides
Mol File: 76674-21-0.mol
Flutriafol Structure
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
form neat
pka 11.60±0.29(Predicted)
Water Solubility 130 mg l-1 (pH 7,20 °C)
Merck 13,4240
BRN 8155287
Stability: Stable. Incompatible with strong oxidizing agents.
InChIKey JWUCHKBSVLQQCO-UHFFFAOYSA-N
CAS DataBase Reference 76674-21-0(CAS DataBase Reference)
NIST Chemistry Reference Flutriafol(76674-21-0)
EPA Substance Registry System Flutriafol (76674-21-0)
Safety Information
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)
MSDS Information
Flutriafol Usage And Synthesis
Chemical Properties solid
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.
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.
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).
China
