Flusilazole

Bezeichnung:Flusilazole

CAS-Nr85509-19-9

Englisch Name:Flusilazole

CBNumberCB8339580

SummenformelC16H15F2N3Si

Molgewicht315.4

MOL-Datei85509-19-9.mol

Flusilazole physikalisch-chemischer Eigenschaften

Schmelzpunkt	55°
Siedepunkt	393 °C [760mmHg]
Dichte	1.17
Dampfdruck	3.9 x l0^-8 Pa (25 °C)
Brechungsindex	1.563
Flammpunkt	192°C
storage temp.	0-6°C
Löslichkeit	DMSO : 100 mg/mL (317.07 mM; Need ultrasonic)
pka	2.5 at 25℃
Wasserlöslichkeit	900 mg l^-1 (pH 1.1), 50 mg l^-1 (pH 5.7), 45 mg l^-1 (pH 7.8) at 25 °C
Aggregatzustand	Solid
Farbe	White to off-white
Merck	13,4232
BRN	5824097
CAS Datenbank	85509-19-9(CAS DataBase Reference)
EPA chemische Informationen	Flusilazole (85509-19-9)

Sicherheit

Kennzeichnung gefährlicher	T;N,N,T
R-Sätze:	61-22-40-51/53
S-Sätze:	53-45-61
RIDADR	UN 2588
WGK Germany	3
RTECS-Nr.	XZ4105000
Toxizität	LD50 in male, female rats (mg/kg): 1110, 674 orally; in rabbits >2000 dermally (Fort, Moberg)

Gefahreninformationscode (GHS)

Flusilazole Chemische Eigenschaften,Einsatz,Produktion Methoden

R-Sätze Betriebsanweisung:
R61:Kann das Kind im Mutterleib schädigen.
R22:Gesundheitsschädlich beim Verschlucken.
R40:Verdacht auf krebserzeugende Wirkung.
R51/53:Giftig für Wasserorganismen, kann in Gewässern längerfristig schädliche Wirkungen haben.
S-Sätze Betriebsanweisung:
S53:Exposition vermeiden - vor Gebrauch besondere Anweisungen einholen.
S45:Bei Unfall oder Unwohlsein sofort Arzt zuziehen (wenn möglich, dieses Etikett vorzeigen).
S61:Freisetzung in die Umwelt vermeiden. Besondere Anweisungen einholen/Sicherheitsdatenblatt zu Rate ziehen.
Chemische Eigenschaften
Brown-red viscous liquid
Verwenden
Agricultural fungicide.
Verwenden
Flusilazole is a silicon-containing triazole fungicide. Flusilazole is used to control fungal infections on a variety of fruit and vegetable crops
Verwenden
Flusilazole is a broad spectrum fungicide used to control fungal disease caused by pathogens of the Ascomycetes, Basidiomycetes and Deuteromycetes families. Flusilazole exhibits curative and preventative activities and is recommended for use in agriculture, horticulture and viticulture. Diseases controlled include eyespot, mildew, and rusts of cereals, cercospora and rust of sugar beets, leaf spots of oilseed rape, scab and mildew of pome and stone fruits, mildew and black rot of grapes and Sigatoka disease of bananas.
Definition
ChEBI: Flusilazole is an organosilicon compound that is dimethylsilane in which the hydrogens attached to the silicon are replaced by p-fluorophenyl groups and a hydrogen attached to one of the methyl groups is replaced by a 1H-1,2,4-triazol-1-yl group. It is a broad-sepctrum fungicide used to protect a variety of crops. It has a role as a xenobiotic, an environmental contaminant, an EC 1.14.13.70 (sterol 14alpha-demethylase) inhibitor and an antifungal agrochemical. It is a member of monofluorobenzenes, a member of triazoles, an organosilicon compound, a conazole fungicide and a triazole fungicide.
Stoffwechselwegen
Flusilazole is stable to aqueous hydrolytic and photolytic degradation. Although flusilazole is relatively stable in soil and is detected in plant and animal samples, numerous degradation products have been reported. The primary metabolic pathway involves the cleavage of the methylenesilicon or/and methylene-triazole linkage. Another primary pathway involves aryl hydroxylation followed by conjugation. The primary metabolic/degradation pathways of flusilazole in soil, plant and animals are presented in Scheme 1.
Degradation
Aqueous hydrolysis and photolysis are not sigruficant degradation pathways for flusilazole (1). Flusilazole was stable (<5% decomposition) in sterile buffers at pH 5, 7 and 9 (25 °C) for 34 days (Cadwgan, 1983). No significant degradation was observed when fusilazole was irradiated with simulated sunlight for 30 days at 300-450 nm in sterile buffer solution at pH 7 (Carter, 1986).

Flusilazole Upstream-Materialien And Downstream Produkte

Flusilazole Anbieter Lieferant Produzent Hersteller Vertrieb Händler.

85509-19-9, Flusilazole Verwandte Suche:

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