Etofenprox

Bezeichnung:Etofenprox

CAS-Nr80844-07-1

Englisch Name:Etofenprox

CBNumberCB8706849

SummenformelC25H28O3

Molgewicht376.49

MOL-Datei80844-07-1.mol

Etofenprox physikalisch-chemischer Eigenschaften

Schmelzpunkt	36.4-38.0°
Siedepunkt	445.03°C (rough estimate)
Dichte	1.1386 (rough estimate)
Dampfdruck	32×10^-3 Pa (100 °C)
Brechungsindex	nD20.2 1.5732
storage temp.	Sealed in dry,Room Temperature
Löslichkeit	DMSO: 100 mg/mL (265.61 mM)
Wasserlöslichkeit	<0.001 mg l^-1(25 °C)
Stabilität	Stable. Incompatible with strong oxidizing agents.
CAS Datenbank	80844-07-1(CAS DataBase Reference)
NIST chemische Informationen	Etofenprox(80844-07-1)
EPA chemische Informationen	Etofenprox (80844-07-1)

Sicherheit

RIDADR	UN 3077 9 / PGIII
WGK Germany	2
RTECS-Nr.	DA0670000
Toxizität	LD50 in rats, mice (mg/kg): >2880, >107200 orally; >2140, >2140 dermally

Gefahreninformationscode (GHS)

Etofenprox Chemische Eigenschaften,Einsatz,Produktion Methoden

Chemische Eigenschaften
solid
Verwenden
Insecticide.
Verwenden
Etofenprox is used to control a wide variety of insects on fruit, tea, soyabeans and many vegetables. It is also used in public health and animal health.
Definition
ChEBI: An aromatic ether that is the 3-phenoxybenzyl ether of 2-(4-ethoxyphenyl)-2-methylpropan-1-ol.
Landwirtschaftliche Anwendung
Insecticide: Approved for use in the U.S. and more than a dozen EU countries.
Handelsname
MTI 500®; PUNKASO®; TREBON®; ZOECON® RF-316
Stoffwechselwegen
Etofenprox is one of the few members of a new class, the non-ester pyrethroids. It lacks the ester bond and therefore is not subject to facile chemical or biochemical hydrolysis. Metabolic options will be limited to oxidative processes. Little has been published in the scientific literature. Its photochemistry has been described and metabolic oxidation products have been noted.
Degradation
Etofenprox is stable in acid and alkaline media for more than 100 days at 80 °C. It is reasonably stable to light under normal conditions of use but it is photodegradable. Under conditions where allethrin was degraded with a half-life of 0.5 hours, etofenprox had a half-life of 3 hours (Tsao and Eto, 1990).
The major product was the ester formed by oxidation at the benzylic carbon atom to form 2-(4-ethoxyphenyl)-2-methylpropyl 3-phenoxybenzoate (2), clearly the result of hydroxylation and dehydrogenation. This ester was found to be non-toxic to houseflies. It was cleaved to form 3PBA (5) and the alcohol (6). 6 was degraded via decarboxylation to 7 and 8. A concurrent reaction of etofenprox was O-de-ethylation to the phenol (3). A similar array of products was seen in both aqueous suspension and as a thin film on glass. It should be noted that this study did not utilise radiolabelled compound.

Etofenprox Upstream-Materialien And Downstream Produkte

Etofenprox Anbieter Lieferant Produzent Hersteller Vertrieb Händler.

80844-07-1, Etofenprox Verwandte Suche:

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