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FENBUCONAZOLE

FENBUCONAZOLE Structure
CAS No.
114369-43-6
Chemical Name:
FENBUCONAZOLE
Synonyms
INDAR;TROIKA;Indar 5;INDAR(R);ENABLE(R);GOVERN(R);FENETHANIL;FENBUCONAZOL;FENBUCONAZOLE;Fenbuconazole [iso]
CBNumber:
CB7405237
Molecular Formula:
C19H17ClN4
Molecular Weight:
336.82
MOL File:
114369-43-6.mol
MSDS File:
SDS
Modify Date:
2023/5/15 10:43:18

FENBUCONAZOLE Properties

Melting point 125.0℃
Boiling point 507.14°C (rough estimate)
Density 1.1288 (rough estimate)
vapor pressure 5 x l0-6 Pa (20 °C)
refractive index 1.6110 (estimate)
storage temp. 0-6°C
solubility Chloroform (Slightly), DMSO (Slightly)
Water Solubility 0.2 mg l-1 (25 °C)
pka 2.34±0.10(Predicted)
BRN 8333667
LogP 3.79 at 20℃
EPA Substance Registry System Fenbuconazole (114369-43-6)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS09
Signal word  Warning
Hazard statements  H410
Precautionary statements  P273-P391-P501
Hazard Codes  N
Risk Statements  50/53
Safety Statements  60-61
RIDADR  UN 3077 9/PG 3
WGK Germany  2
RTECS  XZ5257500
Toxicity LD50 in rats (mg/kg): >2000 orally; >5000 dermally (Driant)

FENBUCONAZOLE price More Price(1)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) 31654 Fenbuconazol PESTANAL?, analytical standard 114369-43-6 100MG ₹6559.95 2022-06-14 Buy
Product number Packaging Price Buy
31654 100MG ₹6559.95 Buy

FENBUCONAZOLE Chemical Properties,Uses,Production

Uses

Fenbuconazole is a conazole based fungicide used as a spray for the control of leaf spot, yellow and brown rust, powdery mildew and net blotch on wheat and barley and apple scab, pear scab and apple p owdery mildew on apples and pears.

Metabolic pathway

A number of sites in the fenbuconazole molecule are susceptible to enzymic attack. Consequently, a large variety of metabolites may be formed by oxidative attack on the phenolic rings or the aliphatic benzylic carbon atom adjacent to the 4-chlorophenyl ring. In mammals, oxidation at the benzylic carbon atom is an important pathway, which gives rise to the corresponding alcohol or ketone. This pathway also leads to lactone formation via hydrolysis of the nitrile group and elimination of a molecule of water. The alcohol may also form conjugates with glucuronic or sulfuric acid. Additional reactions in mammals involve hydroxylation of the phenolic rings.
In plants, oxidation at the benzylic carbon is an important step to further metabolites and cleavage of the linkage to the triazole ring generates triazole, which is subsequently incorporated in a number of metabolic products. Information presented in this entry is based on the PSD Evaluation (PSD, 1995).

Degradation

Fenbuconazole is thermally stable up to 150 °C and there was no observed degradation when fenbuconazole was incubated in the dark in aqueous solutions at pH 5,7 and 9 for up to 30 days at 25 °C.
When an aqueous solution of fenbuconazole (concentration 1.5μg ml-1, pH 7) was irradiated with a xenon arc lamp (filtered to remove wavelengths below 290 nm), the overall radioactivity was 105% of the original amount and the only compound detected was fenbuconazole.

FENBUCONAZOLE Preparation Products And Raw materials

Raw materials

Preparation Products

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1H-1,2,4-Triazole-1-propanenitrile, .alpha.-2-(4-chlorophenyl)ethyl-.alpha.-phenyl- 4-(4-Chlorophenyl)-2-phenyl-2-(1H-1,2,4-tri-azole-1-ylmethyl)butyronitrile Fenbuconazole 100mg [114369-43-6] Fenbuconazol solution ENABLE(R) FENBUCONAZOL FENBUCONAZOLE FENETHANIL GOVERN(R) INDAR INDAR(R) aplha-[2-(4-Chlorophenyl)ethyl]-alpha-phenyl-1H-1,2,4-triazole-1-propanenitrile Fenbuconazole [iso] Indar 5 ALPHA-(3-(4-CHLOROPHENYL)ETHYL-ALPHA-PHENYL)-(1H-1,2,4-TRIAZOLE)-1-PROPANENITRILE 4-(4-CHLOROPHENYL)-2-PHENYL-2-[1H-1,2,4-TRIAZOL-1-YLMETHYL]-BUTANENITRILE TROIKA 1h-1,2,4-triazole-1-propanenitrile,alpha-(2-(4-chlorophenyl)ethyl)-alpha-pheny 4-(4-chlorophenyl)-2-phenyl-2-(1h-1,2,4-triazol-1-ylmethyl)butyronitrile 4-triazole-1-propanenitrile,alpha-(2-(4-chlorophenyl)ethyl)-alpha-phenyl-1h-2 alpha-(2-(4-chlorophenyl)ethyl)-alpha-phenyl-1h-1,2,4-triazole-1-propanenitr FENBUCONAZOLE, 100MG, NEAT FENBUCONAZOL PESTANAL, 100 MG Fenbuconazole Solution, 1000ppm Fenbuconazole @100 μg/mL in MeOH Fenbuconazole@1000 μg/mL in Acetone Fenbuconazole Standard FenbuconazoleSolution,100mg/L,1ml FenbuconazoleSolution,10mg/L,1ml 1H-1,2,4-Triazole-1-propanenitrile, α-[2-(4-chlorophenyl)ethyl]-α-phenyl- FenbuconazoleQ: What is Fenbuconazole Q: What is the CAS Number of Fenbuconazole Q: What is the storage condition of Fenbuconazole Q: What are the applications of Fenbuconazole 2-((1H-1,2,4-Triazol-1-yl)methyl)-4-(4-chlorophenyl)-2-phenylbutanenitrile Resorcinol Impurity 41 Fenbuconazole Solution in Methanol Fenbuconazole Solution in Acetonitrile 1H-1,2,4-Triazole-1-propanenitrile, α-[2-(4-chlorophenyl)ethyl]-α-phenyl- 114369-43-6 C19H17ClN4 Alpha sort ConazolesPesticides&Metabolites E-GAlphabetic F FA - FL Fungicides Pesticides ConazolesAlphabetic