Etofenprox Property

Melting point:

36.4-38.0°

Boiling point:

445.03°C (rough estimate)

Density 

1.1386 (rough estimate)

vapor pressure 

32×10^-3 Pa (100 °C)

refractive index 

nD20.2 1.5732

storage temp. 

Sealed in dry,Room Temperature

solubility 

DMSO: 100 mg/mL (265.61 mM)

form 

Solid

Water Solubility 

<0.001 mg l^-1(25 °C)

color 

Off-white to light yellow

Stability:

Stable. Incompatible with strong oxidizing agents.

CAS DataBase Reference

80844-07-1(CAS DataBase Reference)

NIST Chemistry Reference

Etofenprox(80844-07-1)

EPA Substance Registry System

Etofenprox (80844-07-1)

Safety

RIDADR 

UN 3077 9 / PGIII

WGK Germany 

2

RTECS 

DA0670000

Toxicity

LD50 in rats, mice (mg/kg): >2880, >107200 orally; >2140, >2140 dermally

Hazard and Precautionary Statements (GHS)

Symbol(GHS)

Signal word

Warning

Hazard statements

H362May cause harm to breast-fed children

H410Very toxic to aquatic life with long lasting effects

Precautionary statements

P201Obtain special instructions before use.

P260Do not breathe dust/fume/gas/mist/vapours/spray.

P263Avoid contact during pregnancy/while nursing.

P273Avoid release to the environment.

P308+P313IF exposed or concerned: Get medical advice/attention.

P391Collect spillage. Hazardous to the aquatic environment

Etofenprox Chemical Properties,Usage,Production

Description

Etofenprox belongs to a pyrethroid derivative that is commonly used as an insecticide in agriculture, horticulture, viticulture, forestry, animal health and public health against various insect pests. It can be found as an active ingredient in a variety of pest control products, which is effective to control broad spectrum of pests, such as crawling and flying insects. In the field of agriculture, etofenprox can be applied on a broad range of crops, including rice, fruits, vegetables, corn, soybeans and tea, which is poorly absorbed by roots and little translocation occurs within plants. It is also used for the public health by controlling adult mosquitoes, non biting midges, biting and non-biting flies, which may carry the pathogen. Besides, etofenprox can be found as an component in flea and tick medications for dogs and cats.
Etofenprox is a new type of insecticide with low mammalian toxicity, which can be decomposed in soil by anaerobic and aerobic microorganisms. It functions by strongly disrupting the transmission of nervous impulses and causes paralysis and death to the target insect.

Chemical Properties

solid

Uses

Insecticide.

Uses

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.

Agricultural Uses

Insecticide: Approved for use in the U.S. and more than a dozen EU countries.

Trade name

MTI 500®; PUNKASO®; TREBON®; ZOECON® RF-316

Metabolic pathway

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.