3-Chlor-4-(chlormethyl)-1-[3-(trifluormethyl)phenyl]pyrrolidin-2-on Chemische Eigenschaften,Einsatz,Produktion Methoden
R-Sätze Betriebsanweisung:
R36/37/38:Reizt die Augen, die Atmungsorgane und die Haut.
S-Sätze Betriebsanweisung:
S26:Bei Berührung mit den Augen sofort gründlich mit Wasser abspülen und Arzt konsultieren.
S27:Beschmutzte, getränkte Kleidung sofort ausziehen.
S36/37/39:Bei der Arbeit geeignete Schutzkleidung,Schutzhandschuhe und Schutzbrille/Gesichtsschutz tragen.
Chemische Eigenschaften
Brown solid. Easily soluble in acetone, chlorobenzene, ethanol, xylene and other organic solvents, with a solubility of 100-150g/L. Solubility in kerosene <5g/L. The solubility in water is 28mg/L. Partition coefficient (n-octanol/water) 2300 (20°C). The half-life is 7d at 60°C and pH 4, 18d at 60°C and pH 7, and the half-life in soil is 11-100d.
Verwenden
Flurochloridone (FLC) is a monophenyl pyrrolidinone selective herbicide that can be used in herbicidal composition to control weed in crop fields. It is commonly used to inhibit weeds that occur during the growth of crop plants, such as grains, sunflowers, and potatoes.
Definition
ChEBI: Flurochloridone is a member of pyrrolidines, a member of (trifluoromethyl)benzenes and an organochlorine compound. It has a role as a carotenoid biosynthesis inhibitor, an agrochemical and a herbicide.
Stoffwechselwegen
From hydrolytic and photolytic studies of
flurochloridone in buffer solution, no hydrolysis of
flurochloridone occurs at pH 5, 7, or 9 at 25°C or at
pH 5 at 40°C. Appreciable hydrolysis occurs at
40°C at pH 7 and 9 with half-lives of 190 and
140 days, respectively. Five hydrolytic degradation
products and six photolytic degradation products are
identified. The major photolytic degradation product
which contains 39% of the radioactivity is
4-(chloromethyl)-3-hydroxy-1-[3-
(trifluoromethyl)phenyl]-2-pyrrolidinone with a mixture
of cis and trans isomers. The formation of this major
degradation product suggests that the major
photolytic pathway involves homolytic cleavage of the
carbon ? chlorine bond at the 3-position of the
pyrrolidinone ring and the free radical intermediate can react with water to give the major product or
eliminate the hydrogen radical to form 4-
(chloromethyl)-1,5-dihydro-1-[3-
(trifluoromethyl)phenyl]pyrrol-2H-one.
Mode of action
Flurochloridone is the active substance of some pre-emergence herbicides. It has an inhibitory effect on the synthesis of carotenoids, which protect chlorophylls against oxidative stress.
Toxicity evaluation
The acute oral LD50 of male rats is 4000 mg/kg, the acute transdermal LD50 of rabbits is >5000 mg/kg, and the acute inhalation of rats is LC50 10.3 mg/L (4h). Slightly irritating to rabbit skin and eyes.
3-Chlor-4-(chlormethyl)-1-[3-(trifluormethyl)phenyl]pyrrolidin-2-on Upstream-Materialien And Downstream Produkte
Upstream-Materialien
Downstream Produkte
