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fenvalerate 92%TC 20%EC 200 G/L EC cas no 51630-58-1 51630-58-1 C25H22ClNO3
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Phenvalerate Basic information |
Product Name: | Phenvalerate |
Synonyms: | (cyano(3-phenoxyphenyl)methyl-4-chloro-alpha-(1-methylethyl)phenylacetate);(R,S)-.alpha.-Cyano-3-phenoxybenzyl(R,S)-2-(4-chlorophenyl)-3-methylbutyricester;(rs)-alpha-cyano-3-phenoxybenzyl(rs)-2-(4-chlorophenyl)-3-methylbutyrate;4-chloro-alpha-(1-methylethyl)-benzeneaceticacicyano(3-phenoxyphenyl)meth;4-chloro-alpha-(1-methylethyl)-benzeneaceticacicyano(3-phenoxyphenyl)methylester;4-chloro-alpha-(1-methylethyl)benzeneaceticacid,cyano(3-phenoxyphenyl)methyl;4-chloro-alpha-(1-methylethyl)benzeneaceticacidcyano(3-phenoxyphenyl)methyle;agrofen |
CAS: | 51630-58-1 |
MF: | C25H22ClNO3 |
MW: | 419.9 |
EINECS: | 257-326-3 |
Product Categories: | Agro-Chemicals;INSECTICIDE;Agro-Products;Aromatics;NULL |
Mol File: | 51630-58-1.mol |
Phenvalerate Chemical Properties |
bp | 300°C |
storage temp. | −20°C |
Merck | 13,4038 |
NIST Chemistry Reference | Benzeneacetic acid, 4-chloro-«alpha»-(1-methylethyl)-, cyano(3-phenoxyphenyl)methyl ester(51630-58-1) |
EPA Substance Registry System | Benzeneacetic acid, 4-chloro-.alpha.-(1-methylethyl)-, cyano(3-phenoxyphenyl)methyl ester(51630-58-1) |
Safety Information |
Hazard Codes | T,N |
Risk Statements | 25-36/37/38-50/53-57 |
Safety Statements | 26-45-60-61 |
RIDADR | UN 2811 6.1/PG 3 |
WGK Germany | 3 |
RTECS | CY1576350 |
HazardClass | 6.1(b) |
PackingGroup | III |
Hazardous Substances Data | 51630-58-1(Hazardous Substances Data) |
MSDS Information |
Provider | Language |
---|---|
SigmaAldrich | English |
Phenvalerate Usage And Synthesis |
Chemical Properties | Viscous Yellow Oil |
Usage | An insecticide, used to control insects from food crops, animal feed and cotton products. |
General Description | A clear viscious yellow liquid with a mild odor. Used as broad spectrum insecticide. |
Air & Water Reactions | Insoluble in water. Rapidly hydrolyzed by alkaline solution. |
Reactivity Profile | A pyrethroid. Phenvalerate is an ester and nitrile. Esters react with acids to liberate heat along with alcohols and acids. Strong oxidizing acids may cause a vigorous reaction that is sufficiently exothermic to ignite the reaction products. Heat is also generated by the interaction of esters with caustic solutions. Flammable hydrogen is generated by mixing esters with alkali metals and hydrides. Nitriles may polymerize in the presence of metals and some metal compounds. They are incompatible with acids; mixing nitriles with strong oxidizing acids can lead to extremely violent reactions. Nitriles are generally incompatible with other oxidizing agents such as peroxides and epoxides. The combination of bases and nitriles can produce hydrogen cyanide. Nitriles are hydrolyzed in both aqueous acid and base to give carboxylic acids (or salts of carboxylic acids). |
Phenvalerate Preparation Products And Raw materials |
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