3-Cyclohexyl-6-dimethylamino-1-methyl-1,2,3,4-tetrahydro-1,3,5-triazin-2,4-dion Chemische Eigenschaften,Einsatz,Produktion Methoden
R-Sätze Betriebsanweisung:
R22:Gesundheitsschädlich beim Verschlucken.
R36:Reizt die Augen.
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
Hexazinone is a triazine compound used as a preemergence or postemergence herbicide to control many annual grasses and broad-leaved weeds in noncropped land and certain crops such as alfalfa, blueberries, coffee, pecans and sugarcane
Vorbereitung Methode
Hexazinone is a postemergence contact herbicide effective
against many annual and biennial weeds and, except for
Johnson grass, most perennial weeds. Human contact is
likely at the use stage, and dermal contact and inhalation
are of most concern.
Allgemeine Beschreibung
White crystalline solid. Corrosive eye irritant. Used as an herbicide.
Air & Water Reaktionen
Water soluble. Rapidly decomposed in solution by strong acids and bases.
Reaktivität anzeigen
A triazine.
Carcinogenicity
No carcinogenicity was detected
among pups of rats fed up to 5000 ppm for 2 years.
Similarly, no increase in tumors was produced by feeding up
to 10,000 ppm hexazinone to mice.
Environmental Fate
Soil/
Plant. Biodegrades in soil and natural waters releasing carbon dioxide. The reported half-life in soil is 1 to 6 months (Hartley and Kidd, 1987). Rhodes (1980a) found that the persistence of hexazinone varied from 4 weeks in a Delaware sandy loam to 24 weeks in a Mississippi silt loam.
Hexazinone is subject to microbial degradation (Rhodes, 1980a; Feng, 1987). Metabolites identified in soils, alfalfa and/or sugarcane include 3-(4-hydroxycyclohexyl)-6(dimethylamino)-1-methyl-1,3,5-triazine-2,4(1H,3H)-dione, 3-cyclohexyl-6-(methylamino)-1
Feng (1987) monitored the persistence and degradation of hexazinone in a silt loam soil 104 days after treatment of the herbicide. After 104 days, 66% of the hexazinone degraded via hydroxylation to form the major metabolite 3-(4-hydroxycyclohexyl)-6(dime
No traces of hexazinone or its metabolites were detected on treated blueberries (Jenson and Kimball, 1985).
Photolytic. Photodegradation products identified in aqueous hexazinone solutions following exposure to UV light (λ = 300–400 nm) were 3-(4-hydroxycyclohexyl)-6-(dimethylamino)-1-methyl-1,3,5-triazine-2,4(1H,3H)-dione, 3-cyclohexyl-6-(methylamino)
Stoffwechselwegen
In clay and sand soils, hexazinone is metabolized by
hydroxylation at the 4-position of the cyclohexane ring
and mono-N-demethylation to give [3-(4-
hydroxycyclohexyl)-6-(dimethylamino)-1-methyl-1,3,5-
triazine-2,4-(1H,3H )-dione], and [3-cyclohexyl-6-
(methylamino)-1-methyl-1,3,5-triazine-2,4-(1H,3H )-
dione, respectively. N-Demethylated metabolite is
found in a comparatively higher percentage than the
hydroxylated metabolite in both clay and sand soils.
3-Cyclohexyl-6-dimethylamino-1-methyl-1,2,3,4-tetrahydro-1,3,5-triazin-2,4-dion Upstream-Materialien And Downstream Produkte
Upstream-Materialien
Downstream Produkte
