Tebuconazole

Bezeichnung:Tebuconazole

CAS-Nr107534-96-3

Englisch Name:Tebuconazole

CBNumberCB1350463

SummenformelC16H22ClN3O

Molgewicht307.82

MOL-Datei107534-96-3.mol

Tebuconazole physikalisch-chemischer Eigenschaften

Schmelzpunkt	102-105°C
Siedepunkt	476.9±55.0 °C(Predicted)
Dichte	1.25
Dampfdruck	1.7 x l0^-6 Pa (20 °C)
Brechungsindex	1.5800 (estimate)
Flammpunkt	100 °C
storage temp.	Sealed in dry,2-8°C
Löslichkeit	Chloroform: Slightly Soluble; Methanol: Slightly Soluble
Aggregatzustand	Solid
pka	13.70±0.29(Predicted)
Farbe	White to Almost white
Wasserlöslichkeit	32 mg/L at 20 ºC
Merck	14,9092
InChIKey	PXMNMQRDXWABCY-UHFFFAOYSA-N
LogP	3.700
CAS Datenbank	107534-96-3(CAS DataBase Reference)
NIST chemische Informationen	Tebuconazole(107534-96-3)
EPA chemische Informationen	Tebuconazole (107534-96-3)

Sicherheit

Kennzeichnung gefährlicher	Xn;N,N,Xn
R-Sätze:	22-51/53-63
S-Sätze:	2-22-36/37-61
RIDADR	UN 3077 9/PG 3
WGK Germany	3
RTECS-Nr.	XZ4803270
HazardClass	9
PackingGroup	III
HS Code	29339900
Giftige Stoffe Daten	107534-96-3(Hazardous Substances Data)
Toxizität	bird - domestic,LD50,oral,> 1gm/kg (1000mg/kg),Pesticide Manual. Vol. 9, Pg. 785, 1991.

Gefahreninformationscode (GHS)

Tebuconazole Chemische Eigenschaften,Einsatz,Produktion Methoden

R-Sätze Betriebsanweisung:
R22:Gesundheitsschädlich beim Verschlucken.
R51/53:Giftig für Wasserorganismen, kann in Gewässern längerfristig schädliche Wirkungen haben.
R63:Kann das Kind im Mutterleib möglicherweise schädigen.
S-Sätze Betriebsanweisung:
S2:Darf nicht in die Hände von Kindern gelangen.
S22:Staub nicht einatmen.
S36/37:Bei der Arbeit geeignete Schutzhandschuhe und Schutzkleidung tragen.
S61:Freisetzung in die Umwelt vermeiden. Besondere Anweisungen einholen/Sicherheitsdatenblatt zu Rate ziehen.
Chemische Eigenschaften
White Solid
Verwenden
Fungicide.
Verwenden
Tebuconazole used as a seed dressing is effective against various smut and bunt diseases of cereals. Used as a spray it controls numerous pathogens in various crops: rust species, powdery mildew, Rhyncosporum secalis, Sqtoria spp., Pyrenophora spp., Fusarium spp. in cereals, Mycosphaerella spp. in bananas, Pucciniu spp. and Sclerufium roIfsii in peanuts.
Verwenden
Ergosterol biosynthesis inhibitor. Fungicide.
Verwenden
A triazole fungicide showing potential carcinogenicity
Definition
ChEBI: 1-(4-chlorophenyl)-4,4-dimethyl-3-(1H-1,2,4-triazol-1-ylmethyl)pentan-3-ol is a tertiary alcohol that is pentan-3-ol substituted by a 4-chlorophenyl, methyl, methyl, and a 1H-1,2,4-triazol-1-ylmethyl at positions 1, 4, 4 and 3 respectively. It is a member of monochlorobenzenes, a member of triazoles and a tertiary alcohol.
Landwirtschaftliche Anwendung
Fungicide, Plant growth regulator: Used as a seed treatment against smuts and bunts of cereals; as a foliar spray against diseases of cereal, peanuts, oilseed rape, grapes, bananas, stone fruit, and pome fruit. Registered for use in EU countries. Registered for use in the U.S.
Handelsname
BAY®-HWG 1608; BAYER®-HWG-1608 CORAIL®; ELITE®; FOLICUR®; FOLITRAZOLE®; GAUCHO®; HORIZON®; HWG 1608®; LYNX-1.2®; PREVENTOL® RAXIL (tebuconazole + metalaxyl); SILVACUR®; TEBUJECT®; WOLMAN®; WOODLIFE®
Stoffwechselwegen
Tebuconazole is degraded in soils and does not accumulate. In plants the metabolites were mainly compounds containing triazole, and in mammals tebuconazole was rapidly metabolised and excreted in urine and faeces.
Degradation
Tebuconazole is stable to elevated temperatures. Under sterile conditions it is stable to hydrolysis in water. It is hydrolysed slowly with a DTS0 of >1 year.
Only two products were formed by irradiation of a suspension of tebuconazole in water with UV light (>280 nm). These were the hydrochloride (3) and 1,2,4-triazole (2). The expected product in which chlorine was replaced by hydroxyl could not be isolated. In organic solvents a number of products were formed. Several products (3, 4, 5, 6, 7, 8, 9, 12, 13, 14) were isolated from benzene after 72 hours irradiation (>280 nm). In a number of cases products isolated from photolysis in benzene were formed by reactions in which the solvent participated and involved addition of a benzene molecule (4, 9, 5, 6). On irradiation in methylene chloride and methanol, 4-chloracetophenone (10) and acetophenone (11) were also identified in addition to starting material and 1,2,4-triazole (Wamhoff et al., 1994).

Tebuconazole Upstream-Materialien And Downstream Produkte

Tebuconazole Anbieter Lieferant Produzent Hersteller Vertrieb Händler.

107534-96-3, Tebuconazole Verwandte Suche:

Send Inquriy