3-Phenoxybenzyl-3-(2,2-dichlorvi-nyl)-2,2-dimethyl-cyclopropancar-boxylat Chemische Eigenschaften,Einsatz,Produktion Methoden
ERSCHEINUNGSBILD
GELBBRAUNE BIS BRAUNE, VISKOSE FLüSSIGKEIT ODER KRISTALLE.
CHEMISCHE GEFAHREN
Zersetzung beim Verbrennen unter Bildung giftiger Rauche mit Chlorwasserstoff.
ARBEITSPLATZGRENZWERTE
TLV nicht festgelegt (ACGIH 2005).
AUFNAHMEWEGE
Aufnahme in den K?rper durch Inhalation des Aerosols und durch Verschlucken.
INHALATIONSGEFAHREN
Nur ungenügende Angaben vorhanden über die Geschwindigkeit, mit der eine gesundheitssch?dliche Konzentration in der Luft beim Verdampfen bei 20°C erreicht wird.
WIRKUNGEN BEI KURZZEITEXPOSITION
WIRKUNGEN BEI KURZZEITEXPOSITION: Die Substanz reizt die Augen, die Haut und die Atemwege.
LECKAGE
NICHT in die Kanalisation spülen. NICHT in die Umwelt gelangen lassen. Verschüttetes Material in Beh?ltern sammeln; falls erforderlich durch Anfeuchten Staubentwicklung verhindern. Reste sorgf?ltig sammeln. An sicheren Ort bringen. Pers?nliche Schutzausrüstung: Atemschutzger?t, A/P2-Filter für organische D?mpfe und sch?dlichen Staub.
R-S?tze Betriebsanweisung:
R20/22:Gesundheitssch?dlich beim Einatmen und Verschlucken.
R43:Sensibilisierung durch Hautkontakt m?glich.
R50/53:Sehr giftig für Wasserorganismen, kann in Gew?ssern l?ngerfristig sch?dliche 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.
R51/53:Giftig für Wasserorganismen, kann in Gew?ssern l?ngerfristig sch?dliche Wirkungen haben.
R36:Reizt die Augen.
R20/21/22:Gesundheitssch?dlich beim Einatmen,Verschlucken und Berührung mit der Haut.
S-S?tze Betriebsanweisung:
S13:Von Nahrungsmitteln, Getr?nken und Futtermitteln fernhalten.
S24:Berührung mit der Haut vermeiden.
S36/37/39:Bei der Arbeit geeignete Schutzkleidung,Schutzhandschuhe und Schutzbrille/Gesichtsschutz tragen.
S60:Dieses Produkt und sein Beh?lter sind als gef?hrlicher 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 m?glich, dieses Etikett vorzeigen).
S36/37:Bei der Arbeit geeignete Schutzhandschuhe und Schutzkleidung tragen.
S16:Von Zündquellen fernhalten - Nicht rauchen.
S7:Beh?lter dicht geschlossen halten.
S26:Bei Berührung mit den Augen sofort gründlich mit Wasser abspülen und Arzt konsultieren.
Beschreibung
Yellow-brown to brown liquid, which sometimes tends to crystallize at room temperature (technical grade).
Permethrin, a pyrethroid insecticide with little mammalian toxicity, has been marketed as a tick repellent. Permethrin is the only synthetic pyrethroid that is used worldwide for head lice. The spray formulation is the most widely available form. Once applied to clothing, it is stable through several wash cycles. It is also suitable for treating sleeping bags, tents, and fabric used for insect screening. A liquid concentrate has been used to impregnate fabric for as long as the life of the garment. Permethrin is particularly helpful in the prevention of tick and chigger bites. These crawling arthropods must travel across the treated fabric, whereas flying insects tend to be attracted directly to exposed skin. The combination of a DEET-containing repellent and permethrin-treated clothing is generally highly ffective against a wide range of biting arthropods.
Chemische Eigenschaften
Crystalline Solid
Verwenden
Labelled Permethrin (P288500). Synthetic pyrethroid insectide, more stable to light and at least as active as the natural pyrethrins and with low mammalian toxicity.
Indications
Permethrin is a synthetic pyrethroid active against lice, ticks, mites, and fleas. It
acts on neural cellmembranes, delaying repolarization and causing paralysis. The
compound has no reported adverse properties, is heat and light stable, has 70%
to 80% ovicidal activity, and leaves an active residue on the scalp.
Permethrin 0.5% spray kills ticks and repels mosquitoes and stable flies. It is broken
down when applied to skin and, hence, should be applied to clothing, shoes, tents,
and so on. Spray only enough to moisten the material. Spray on clothing at least 2
hours before wearing. One treatment should last through a few washings.
Definition
ChEBI: A cyclopropanecarboxylate ester in which the esterifying alcohol is 3-phenoxybenzyl alcohol and the cyclopropane ring is substituted with a 2,2-dichlorovinyl group and with gem-dimethyl groups.
Allgemeine Beschreibung
Pale brown liquid. Relatively water insoluble. Used as an insecticide.
Air & Water Reaktionen
Insoluble in water.
Reaktivit?t anzeigen
A pyrethroid derivative.
Kontakt-Allergie
Pyrethroids, also called pyrethrinoids, are neurotoxic
synthetic compounds used as insecticides, with irritant
properties. Cypermethrin and fenvalerate have been
reported as causing positive allergic patch tests, but
only fenvalerate was relevant in an agricultural worker.
Pharmakologie
Permethrin is a synthetic pyrethroid that interferes with the influx of sodium
through cell membranes, leading to neurologic paralysis and death of the mite.
There is minimal percutaneous absorption (<2%), which is rapidly hydrolyzed
and excreted in the urine. Permethrin 5% dermal cream (Elimite) is applied for
8 to 12 hours to the entire body from the chin down and is then washed off.
Clinical Use
Permethrin is 3-(2,2-Dichloroethenyl)-2,2-dimethylcyclopropanecarboxylicacid (3-phenoxyphenyl)methylester or 3-(phenoxyphenyl)methyl (±)-cis, trans-3-(2,2-dichloroethenyl)-2,2-dimethylcyclopropanecarboxylate(Nix). This synthetic pyrethrinoid compound is more stablechemically than most natural pyrethrins and is at least as activeas an insecticide. Of the four isomers present, the1(R),trans and 1(R),cis-isomers are primarily responsiblefor the insecticidal activity. The commercial product is amixture consisting of 60% trans and 40% cis racemic isomers.It occurs as colorless to pale yellow low-melting crystalsor as a pale yellow liquid and is insoluble in water butsoluble in most organic solvents.
Permethrin exerts a lethal action against lice, ticks, mites,and fleas. It acts on the nerve cell membranes of the parasitesto disrupt sodium channel conductance. It is used as apediculicide for the treatment of head lice. A single applicationof a 1% solution effects cures in more than 99% ofcases. The most frequent side effect is pruritus, which occurredin about 6% of the patients tested.
Sicherheitsprofil
Poison by inhalation, intravenous, and intracerebral routes. Moderately toxic by ingestion. Experimental reproductive effects. Mutation data reported. A skin irritant. When heated to decomposition it emits toxic fumes of Cl-. See also ESTERS
Environmental Fate
Soil. Permethrin biodegraded rapidly via hydrolysis yielding 3-(2,2-dichloroethenyl)-
2,2-dimethylcyclopropanecarboxylic acid and 3-phenoxybenzyl alcohol (Kaufman et al.,
1981). The reported half-life in soil containing 1.3–51.3% organic matter and pH 4.2–7.7
is <38 days (Worthing and Hance, 1991)
In lake water, permethrin degraded more rapidly than in flooded sediment to transand cis-(dichlorovinyl)dimethylcyclopropanecarboxylic acid. The cis isomer was more
stable toward biological and chemical degradation than the trans isomer (Sharom and
Solom
Plant. Metabolites identified in cotton leaves included trans-hydroxypermethrin, 2′-
hydroxypermethrin, 4′-hydroxypermethrin, dichlorovinyl acid, dichlorovinyl acid conjugates, hydroxydichlorovinyl acid, hydroxydichlorovinyl acid conjugates, phe
Dislodgable residues of permethrin on cotton leaves 0, 24, 48, 72 and 96 hours after
application (1.1 kg/ha) were (cis:trans): 0.26:0.38, 0.24:0.34, 0.22:0.32, 0.16:0.24 and
0.15:0.21 μg/m2, respectively (Buck et al., 1980).
Photolytic. Photolysis of permethrin in aqueous solutions containing various solvents
(acetone, hexane and methanol) under UV light (λ >290 nm) or on soil in sunlight initially
resulted in the isomerization of the cyclopropane moiety and ester cl
Stoffwechselwegen
Permethrin was one of the first photostable pyrethroids suitable for field
use.It served as a precursor for others such as its α-cyano analogue,
cypermethrin. As it lacks the cyano group it has no chirality at the acarbon
atom and therefore consists of a mixture of only four isomers. It is
hydrolysed more readily than cypermethrin because it is an ester of a
primary alcohol.
Much of the early research on the metabolism of the synthetic, photostable
pyrethroids was conducted by Casida and co-workers on permethrin.
The published results greatly assisted subsequent work on the
analogues. This is stressed because some of the information reported
below will draw on the metabolic schemes given in the cypermethrin
entry.
The environmental fate of permethrin and its metabolism in plants,
insects, animals and fish have been reported. The insecticide is metabolised
by ester cleavage to its constituent acid and alcohol and subsequent
conjugation of these. The primary metabolites are also subject to oxidation
prior to conjugation. Permethrin itself is also subject to oxidation, the cisisomers
more so than the trans-isomers because the former is more slowly
hy droly sed.
3-Phenoxybenzyl-3-(2,2-dichlorvi-nyl)-2,2-dimethyl-cyclopropancar-boxylat Upstream-Materialien And Downstream Produkte
Upstream-Materialien
Downstream Produkte
