2-Chlor-N-[[(4-methoxy-6-methyl-1,3,5-triazin-2-yl)amino]carbonyl]benzolsulfonamid 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.
S36:DE: Bei der Arbeit geeignete Schutzkleidung tragen.
S26:Bei Berührung mit den Augen sofort gründlich mit Wasser abspülen und Arzt konsultieren.
Beschreibung
Chlorsulfuron is one of the first sulfonylurea herbicides
developed and commercialized by DuPont. Dr George Levitt
and his team at DuPont first synthesized chlorsulfuron in 1976,
and it was commercialized for use as a herbicide in 1981. It is
currently registered by DuPont in the United States, Canada,
the European Union, Russia, the Ukraine, Australia, New
Zealand, South Africa, Saudi Arabia, and in several countries of
South America.
Compared with many other herbicides that are applied at
levels of pounds per acre (or kilograms per acre), sulfonylureas
are highly effective at use rates of less than an ounce per acre
(approximately 6 g per acre for chlorsulfuron).
Chemische Eigenschaften
Colorless, odorless crystals
Verwenden
Chlorsulfuron is used as a postemergence herbicide for the
control of dicotyledonous weeds, with excellent safety for
wheat and other cereals crops. While chlorsulfuron is primarily
used to control weeds in cereals, it can also be used in range
and pasture applications. It is currently only used to a minor
extent for nonfood industrial applications and right-of-way
purposes.
Allgemeine Beschreibung
Colorless crystals. Non corrosive. Insoluble in water. Used as an herbicide.
Air & Water Reaktionen
Insoluble in water. Reacts slowly with water. The reaction is promoted by acid such that the pH is less than 5.0 (1/2 life of 24-48 hrs.). Reaction is also promoted by polar organic solvents such as methanol and acetone.
Landwirtschaftliche Anwendung
Herbicide: A selective systemic herbicide used to control most
broadleaf weeds and some annual grasses in wheat, barley,
oats, duram, rye, triticale and flax. Applied to non-crop
sites such as rights-of-way, fence rows and roadsides.
Handelsname
DPX 4189®; FINESSE®; GLEAN®;
GLEAN 20DF®; LANDMARK® MP; LASHER®;
RIVERDALE CORSAIR®; TELAR® DF
mögliche Exposition
A selective systemic sulfonylurea herbicide used to control most broadleaf weeds and some annual grasses in wheat, barley, oats, duram, rye, triticale, and flax. Applied to noncrop sites such as rights-of-way, fence rows, and roadsides.
Environmental Fate
Soil. Degrades in soil via hydrolysis followed by microbial degradation forming low
molecular weight, inactive compounds. The estimated half-life was reported to range from
4 to 6 weeks (Hartley and Kidd, 1987; Cremlyn, 1991). Microorganisms capable of
degrading chlorsulfuron are Aspergillis niger, Streptomyces griseolus and Penicillium sp.
(Humburg et al., 1989). One transformation product reported in field soils is 2-chlorobenzenesulfonamide (Smith, 1988)
The reported dissipation rate of chlorsulfuron in surface soil is 0.024/day (Walker and
Brown, 1983). The persistence of chlorsulfuron decreased when soil temperature and
moisture were increased (Walker and Brown, 1983; Thirunarayanan et al., 1985)
Plant. Chlorsulfuron is metabolized by plants to hydroxylated, nonphytotoxic compounds including 2-chloro-N-(((4-methoxy-6-methyl-1,3,5-triazin-2-yl)-amino)carbonyl)benzenesulfonamide (Duke et al., 1991). Devine and Born (1985) and Peterson and
Photolytic. The reported photolysis half-lives of chlorsulfuron in distilled water, methanol and natural creek water at λ >290 nm were 18, 92 and 18 hours, respectively. In all
cases, 2-chlorobenzene sulfonamide, 2-methoxy-4-methyl-6-amino-1,3,5-triazine and
trace amounts of the tentatively identified compound nitroso-2-chlorophenylsulfone
formed as photoproducts (Herrmann et al., 1985).
Stoffwechselwegen
Chlorsulfuron is metabolized in wheat and in tolerant
broadleaves via different pathways where
hydroxylation occurs on the methyl group of the
triazine ring and at the phenyl ring of the chlorsulfuron
in respective plants. With chemical degradation of
chlorsulfuron on dry minerals (Syst.), two pathways of
degradation are observed, one of which is direct
Versand/Shipping
UN3077 Environmentally hazardous substances, solid, n.o.s., Hazard class: 9; Labels: 9-Miscellaneous hazardous material, Technical Name Required.
Inkompatibilitäten
Slowly hydrolyzes in water, releasing ammonia and forming acetate salts. May bencompatible with oxidizers (chlorates, nitrates, peroxides, permanganates, perchlorates, chlorine, bromine, fluorine, etc.); contact may cause fires or explosions. Keep away from alkaline materials, strong bases, strong acids, oxoacids, epoxides.
Waste disposal
It is the responsibility of chemical waste generators to determine the toxicity and physical properties and of a discarded chemical and to properly identify its classification and certification as a hazardous waste and to determine the disposal method. United States Environmental Protection Agency guidelines for the classification determination are listed in 40 CFR Parts 261.3. In addition, waste generators must consult and follow all regional, national, state, and local hazardous waste laws to ensure complete and accurate classification and disposal methods. Recycle any unused portion of the material for its approved use or return it to the manufacturer or supplier. Ultimate disposal of the chemical must consider: the material’s impact on air quality; potential migration in soil or water; effects on animal, aquatic, and plant life; and conformance with environmental and public health regulations
2-Chlor-N-[[(4-methoxy-6-methyl-1,3,5-triazin-2-yl)amino]carbonyl]benzolsulfonamid Upstream-Materialien And Downstream Produkte
Upstream-Materialien
Downstream Produkte
