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)

Flash point:

2 °C

storage temp. 

0-6°C

solubility 

Chloroform (Slightly), DMSO (Slightly), Methanol (Slightly)

form 

Solid

Water Solubility 

130 mg l^-1 (pH 7,20 °C)

pka

11.60±0.29(Predicted)

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)

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)

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

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

Agricultural fungicide.

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(76674-21-0)Related Product Information

• Ethanol
• 2-AMINO-1-PHENYLETHANOL
• Diethanolamine
• Diethylstilbestrol
• 2-Methoxyethanol
• 1,2,4-Triazole
• Monoethanolamine
• Ethyl acetate
• 2-Mercaptoethanol
• Phenylacetone
• 1-(4-Fluorophenyl)ethanol
• 2-FLUOROPHENETHYLAMINE
• 1-(2-Fluorophenyl)ethanol
• 2-AMINO-1-(2-FLUORO-PHENYL)-ETHANOL
• 2-(4-FLUOROPHENYL)-2-PROPANOL
• 4-Fluorophenethylamine
• FLUTRIAFOL PESTANAL, 100 MG
• 4-FLUOROBENZHYDROL