1-((2-(2,4-Dichlorphenyl)-4-pro-pyl-1,3-dioxalan-2-yl)methyl)-1H-1,2,4-triazol Chemische Eigenschaften,Einsatz,Produktion Methoden
R-Sätze Betriebsanweisung:
R22:Gesundheitsschädlich beim Verschlucken.
R43:Sensibilisierung durch Hautkontakt möglich.
R50/53:Sehr giftig für Wasserorganismen, kann in Gewässern längerfristig schädliche Wirkungen haben.
R39/23/24/25:Giftig: ernste Gefahr irreversiblen Schadens durch Einatmen, Berührung mit der Haut und durch Verschlucken.
R23/24/25:Giftig beim Einatmen, Verschlucken und Berührung mit der Haut.
R11:Leichtentzündlich.
S-Sätze Betriebsanweisung:
S36/37:Bei der Arbeit geeignete Schutzhandschuhe und Schutzkleidung tragen.
S46:Bei Verschlucken sofort ärztlichen Rat einholen und Verpackung oder Etikett vorzeigen.
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.
S45:Bei Unfall oder Unwohlsein sofort Arzt zuziehen (wenn möglich, dieses Etikett vorzeigen).
S16:Von Zündquellen fernhalten - Nicht rauchen.
S7:Behälter dicht geschlossen halten.
Beschreibung
Propiconazole is a mixture of four stereoisomers and was first
developed in 1979 by Janssen Pharmaceutical of Belgium.
Chemische Eigenschaften
normally provided as a yellow liquid
Verwenden
Labelled Propiconazole (P770100). Systemic foliar fungicide. Agricultural fungicide.
Allgemeine Beschreibung
Yellowish odorless liquid. Non corrosive. Used as a fungicide.
Reaktivität anzeigen
A triazole derivative.
Landwirtschaftliche Anwendung
Fungicide: Used to control fungi on a broad range of crops and turf. Used on ornamentals, range land and rights-of-way to prevent and control powdery mildew and fungi on hardwoods and conifers.
Handelsname
ALAMO®; BANNER®; BENIT®; BREAK®; BUMPER®; CGA-64250®; CGA-92710 F®; DESMEL®; FIDIS®; JUNO®; MANTI® S; MAXX®; NOVEL®; ORBIT®; PRACTIS®; PROPIMAX®; RADAR®; RESTORE®; SPIRE®; STRATEGO® (trifloxystrobin + propiconazole); TASPA®; TILT®; WOCOSIN®
mögliche Exposition
Propiconazole is a triazole fungicide
used to control fungi on a broad range of crops and turf.
Used on ornamentals, range land and rights-of-way to pre-
vent and control powdery mildew and fungi on hardwoods
and conifers.
Stoffwechselwegen
The numerous metabolites of propiconazole are
identified from rat urine and feces. Major sites for
enzymatic attack are the propyl side chain and the
cleavage of the dioxane ring. The 2,4-dichlorophenyl
ring is attacked in various ways including the formation of a cyclohexadiene ring system, hydroxylation,
replacement of the chlorine substituent by a hydroxy
group, and introduction of a methylthio group. The
1,2,4-triazole ring is oxidatively attacked, leading to
hydroxy derivatives. The vast majority of the alcoholic
and phenolic metabolites are excreted as sulfuric acid
and glucuronic acid conjugates. The major metabolic
pathway in mice is via cleavage of the dioxane ring.
Photolysis causes cleavage of the C1-triazole bond of
propiconazole, liberating 1,2,4-triazole as the major
product. Six more degradation products are identified
which are not included in the mammalian metabolites.
Versand/Shipping
UN3082 Environmentally hazardous substances,
liquid, n.o.s., Hazard class: 9; Labels: 9-Miscellaneous
hazardous material, Technical Name Required. UN3077
Environmentally hazardous substances, solid, n.o.s., Hazard
class: 9; Labels: 9-Miscellaneous hazardous material,
Technical Name Required.
Inkompatibilitäten
The triazoles are sensitive to heat,
friction, and impact. Sensitivity varies with the type
substitution to the triazole ring. Metal chelated and halogen
substitution of the triazol ring make for a particularly heat
sensitive material. Azido and nitro derivatives have been
employed as high explosives. No matter the derivative
these materials should be treated as explosives
Waste disposal
Consult with environmental
regulatory agencies for guidance on acceptable disposal
practices. Contact a licensed disposal facility about surplus
and nonrecyclable solutions. Burn in a chemical incinerator
equipped with an afterburner and scrubber. Extra care must
be exercised as the material in an organic solvent is highly
flammable. In accordance with 40CFR165, follow recom-
mendations for the disposal of pesticides and pesticide con-
tainers. Containers must be disposed of properly by
following package label directions or by contacting your
local or federal environmental control agency, or by con-
tacting your regional EPA office. Incineration or permanga-
nate oxidation.
1-((2-(2,4-Dichlorphenyl)-4-pro-pyl-1,3-dioxalan-2-yl)methyl)-1H-1,2,4-triazol Upstream-Materialien And Downstream Produkte
Upstream-Materialien
Downstream Produkte
