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METOXADIAZONE

METOXADIAZONE Suppliers list
Company Name: TianJin Alta Scientific Co., Ltd.  
Tel: 022-65378550-8551
Email: contact@altascientific.com
Company Name: Alta Scientific Co., Ltd.  
Tel: 022-6537-8550 15522853686
Email: sales@altasci.com.cn
Company Name: Shanghai Jiegu Biotechnology Co., Ltd.  
Tel: 021-51698675
Email: sales@jiejiegroup.com
Company Name: Energy Chemical  
Tel: 021-58432009 400-005-6266
Email: marketing@energy-chemical.com
Company Name: LGC Science (Shanghai) Ltd.  
Tel: 17717235263
Email: offer.de@lgcgroup.com
METOXADIAZONE Basic information
Product Name:METOXADIAZONE
Synonyms:Ars Red;Elemic;RP 32861;S 21074;Valsan;5-methoxy-3-(2-methoxyphenyl)-1,3,4-oxadiazol-2-one;3-(2-methoxyphenyl)-5-methoxy-1,3,4-oxadiazol-2(3H)-one;2-methoxy-4-(o-methoxyphenyl)-delta(sup 2)-1,3,4-oxadiazolin-5-one Elemic
CAS:60589-06-2
MF:C10H10N2O4
MW:222.2
EINECS:
Product Categories:
Mol File:60589-06-2.mol
METOXADIAZONE Structure
METOXADIAZONE Chemical Properties
Boiling point 363.37°C (rough estimate)
density 1.3404 (rough estimate)
refractive index 1.6300 (estimate)
solubility Chloroform (Slightly), Methanol (Slightly)
form Solid
pka-0.95±0.40(Predicted)
color Pale Yellow to Light Brown
Stability:Light Sensitive
CAS DataBase Reference60589-06-2
Safety Information
ToxicityLD50 orl-rat: 175 mg/kg IYKEDH 19,735,88
MSDS Information
METOXADIAZONE Usage And Synthesis
Chemical PropertiesPure product is light yellow to russet crystal or crystalline powder. m.p.79.5°C, vapor pressure 0.147Pa (25°C), relative density 1.401-1.410, ignition point 160°C, ignition temperature 390°C. It is soluble in acetone, ethyl acetate, chloromethane, anisole; more soluble in methanol, xylene, trichloroethane; soluble in ethanol, isopropanol, toluene. Freely soluble in acetone, chloroform, ethyl acetate, chloromethane, anisole; more soluble in methanol, xylene, trichloroethane; soluble in ethanol, isopropanol, trimethylbenzene, alkylbenzene, etc.; almost insoluble in water, cyclohexane, kerosene. Stable at room temperature, unstable at higher than 50°C. By adding Sumillizer-TNP (2%), a stable agent can be obtained. Explosivity is the lower limit of dust explosion. 40 ℃ in the following solvents after 6 months residual rate is: acetone 97.7%, methanol 85.3%, isopropanol 95%, ethyl acetate 99.8%, cyclohexanone 100.5%, xylene 101.0%, chloroform 93.2%, trichloroethane 102.0%, it can be seen that the methanol in the more decomposable in its solvents and stable. The agent is stable in other carriers except unstable in bentonite and sodium carbonate (40℃, 6 residuals of 85.7% and 16. 0% respectively). The xenon lamp irradiation test proved that it will gradually decompose in the light, in addition, humidity also has an effect on the agent.
UsesMetoxadiazone is used as an insecticide used to control rice hoppers, cockroaches and ants.
Production MethodsThe commercial production process of metoxadiazone is not described in open literature. However, the generic process for oxadiazolone insecticides is that they are typically produced by assembling the oxadiazolinone ring from appropriate hydrazide and carbonyl precursors, followed by aryl substitution to introduce the 2 methoxyphenyl group and O methylation to yield the methoxy substituted heterocycle.
DefinitionChEBI: Metoxadiazone is a member of methoxybenzenes.
Mechanism of actionSelective, induces stunting and chlorosis. It works by blocking adrenergic receptors, leading to the relaxation of vascular smooth muscles and inhibition of norepinephrine secretion from the adrenal glands
Safety ProfileA poison by ingestion and subcutaneous routes. Moderately toxic by skin contact. When heated to decomposition it emits toxic vapors of NOx.
Pesticide TypeInsecticide
METOXADIAZONE Preparation Products And Raw materials
Raw materialsPhosgene-->o-Anisidine-->Methyl chloroformate
Tag:METOXADIAZONE(60589-06-2) Related Product Information
3-(4-Aminophenyl)-5-methoxy-1,3,4-oxadiazol-2(3H)-one 5-Methoxy-3-(4-nitrophenyl)-3H-(1,3,4)oxadiazol-2-one ethyl 1-(2-methoxyphenyl)-5-oxo-4,5-dihydro-1H-1,2,4-triazole-3-carboxylate 6-Bromo-2-(2-methoxyphenyl)pyridazin-3(2H)-one 3(2H)-Pyridazinone, 5-bromo-2-(2-methoxyphenyl)- {[1-(2-methoxyphenyl)-1H-pyrazol-4-yl]methyl}amine dihydrochloride