FENBUCONAZOLE

FENBUCONAZOLE Struktur
114369-43-6
CAS-Nr.
114369-43-6
Englisch Name:
FENBUCONAZOLE
Synonyma:
INDAR;TROIKA;Indar 5;INDAR(R);ENABLE(R);GOVERN(R);FENETHANIL;FENBUCONAZOL;FENBUCONAZOLE;Fenbuconazole [iso]
CBNumber:
CB7405237
Summenformel:
C19H17ClN4
Molgewicht:
336.82
MOL-Datei:
114369-43-6.mol

FENBUCONAZOLE Eigenschaften

Schmelzpunkt:
125.0℃
Siedepunkt:
507.14°C (rough estimate)
Dichte
1.1288 (rough estimate)
Dampfdruck
5 x l0-6 Pa (20 °C)
Brechungsindex
1.6110 (estimate)
storage temp. 
0-6°C
Löslichkeit
Chloroform (Slightly), DMSO (Slightly)
Wasserlöslichkeit
0.2 mg l-1 (25 °C)
pka
2.34±0.10(Predicted)
BRN 
8333667
LogP
3.79 at 20℃
EPA chemische Informationen
Fenbuconazole (114369-43-6)
Sicherheit
  • Risiko- und Sicherheitserklärung
  • Gefahreninformationscode (GHS)
Kennzeichnung gefährlicher N
R-Sätze: 50/53
S-Sätze: 60-61
RIDADR  UN 3077 9/PG 3
WGK Germany  2
RTECS-Nr. XZ5257500
Toxizität LD50 in rats (mg/kg): >2000 orally; >5000 dermally (Driant)
Bildanzeige (GHS) GHS hazard pictograms
Alarmwort Warnung
Gefahrenhinweise
Code Gefahrenhinweise Gefahrenklasse Abteilung Alarmwort Symbol P-Code
H410 Sehr giftig für Wasserorganismen mit langfristiger Wirkung. Langfristig (chronisch) gewässergefährdend Kategorie 1 Warnung GHS hazard pictogramssrc="/GHS09.jpg" width="20" height="20" /> P273, P391, P501
Sicherheit
P273 Freisetzung in die Umwelt vermeiden.
P391 Verschüttete Mengen aufnehmen.
P501 Inhalt/Behälter ... (Entsorgungsvorschriften vom Hersteller anzugeben) zuführen.

FENBUCONAZOLE Chemische Eigenschaften,Einsatz,Produktion Methoden

R-Sätze Betriebsanweisung:

R50/53:Sehr giftig für Wasserorganismen, kann in Gewässern längerfristig schädliche Wirkungen haben.

S-Sätze Betriebsanweisung:

S60:Dieses Produkt und sein Behälter sind als gefährlicher Abfall zu entsorgen.
S61:Freisetzung in die Umwelt vermeiden. Besondere Anweisungen einholen/Sicherheitsdatenblatt zu Rate ziehen.

Verwenden

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.

Stoffwechselwegen

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 Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte


FENBUCONAZOLE Anbieter Lieferant Produzent Hersteller Vertrieb Händler.

Global( 93)Lieferanten
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114369-43-6()Verwandte Suche:


  • 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
  • 114369-43-6
  • C19H17ClN4
  • Alpha sort
  • ConazolesPesticides&Metabolites
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  • FA - FL
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