N-[[(4-Chlorphenyl)amino]carbonyl]-2,6-difluorbenzamid 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.
Beschreibung
Diflubenzuron is produced by the reaction of 2,6-difluorobenzamide
with 4-chlorophenylisocyanate. Diflubenzuron
was first registered as a pesticide in the United States in 1979.
Environmental Protection Agency issued a Registration Standard
for diflubenzuron in September 1985 (PB86-176500). In
1991, a Data Call-In was made to require additional residue
chemistry and ecological effects data. The current Reregistration
Eligibility Decision Document was issued in August 1997,
reflecting analysis of the new data.
Verwenden
Diflubenzuron is a benzoylurea-based pesticide belonging to the benzamide class. Diflubenzuron is a chitin synthesis inhibitor. Diflubenzuron is used in both agriculture and forest management to selec
tively control insect pests, particularly moths and weevils.
Definition
ChEBI: A benzoylurea insecticide that is urea in which a hydrogen attached to one of the nitrogens is replaced by a 4-chlorophenyl group, and a hydrogen attached to the other nitrogen is replaced bgy a 2,6-difluorobenzoyl group.
Allgemeine Beschreibung
Colorless to yellow crystals. Used as a selective insecticide.
Air & Water Reaktionen
Hydrolyzed in alkaline solution above pH 9.0.
Reaktivität anzeigen
A urea derivative.
Landwirtschaftliche Anwendung
Insecticide, Larvicide: Diflubenzuron is used primarily on citrus, cattle
feed, cotton, forestry, mushrooms, ornamentals, pastures,
soybeans, standing water, sewage systems, and wide-area
general outdoor treatment sites. The insecticide behaves as
a chitin inhibitor to inhibit the growth of many leaf-eating
larvae, mosquito larvae, aquatic midges, rust mite, boll weevil, and house-black-, and stable-flies. Diflubenzuron was
first registered in the United States in 1979 for use as an
insecticide.
Handelsname
ADEPT®; ASTONEX®; DIMILIN®;
DIMILIN® FLO; DIMILIN® WG-80; DU-112307®;
DUPHAR® PH 60-40; ODC-45®; DIFLURON®;
DU 112307®; LARGON®; LARVAKIL®;
MICROMITE®; OMS 1804®; PDD 60401®; PH 60-
40®; PHILIPS-DUPHAR® PH 60-40; TH 60-40®;
THOMPSON-HAYWARD® 6040; VIGILANTE®
Sicherheitsprofil
Moderately toxic by
skin contact. Mildly toxic by ingestion.
Mutation data reported. When heated to
decomposition it emits very toxic fumes of
Cl-, F-, and NOx.
Environmental Fate
Soil. The half-life in soil is <1 week (Hartley and Kidd, 1987). Di?ubenzuron degrades more rapidly in neutral or basic conditions but more slowly under acidic conditions (pH <6) (Ivie et al., 1980).
Chemical/Physical. Hydrolyzes in water to 4-chlorophenylurea (Verschueren, 1983).
Stoffwechselwegen
Diflubenzuron was the first active substance commercialised as a
benzoylurea insect growth regulator and there is extensive published
information on its degradation and metabolism. Detailed studies of the
degradation in soils have shown that cleavage of the urea linkage is
the major process. This also occurs in plants, insects and mammals but
the formation of products in which diflubenzuron is hydroxylated in
both rings is also an important metabolic process.
N-[[(4-Chlorphenyl)amino]carbonyl]-2,6-difluorbenzamid Upstream-Materialien And Downstream Produkte
Upstream-Materialien
Downstream Produkte
