fenvalerate 92%TC 2...

fenvalerate 92%TC 20%EC 200 G/L EC cas no 51630-58-1
fenvalerate 92%TC 20%EC 200 G/L EC cas no 51630-58-1
fenvalerate 92%TC 20%EC 200 G/L EC cas no 51630-58-1
fenvalerate 92%TC 20%EC 200 G/L EC cas no 51630-58-1

fenvalerate 92%TC 20%EC 200 G/L EC cas no 51630-58-1

Min.Order / FOB Price:Get Latest Price

50 Gram

Negotiable

  • Min.Order :50 Gram
  • Purity: 92%TC 20%EC 200 G/L EC
  • Payment Terms : L/C,D/P,T/T

Keywords

fenvalerate 92%TC 20%EC 200 G/L EC cas no 51630-58-1 51630-58-1 C25H22ClNO3

Quick Details

  • Appearance:light yellow liquid
  • Application:RED SOLID
  • PackAge:as needed
  • ProductionCapacity:500|Kilogram|Month
  • Storage:Store in cool and dry
  • Transportation:by air or sea

Superiority:

2.Our product feature:

As a leading manufacturer in China, we can provide high quality goods at the lowest price upon your requests. Our company mainly supply products as follows: anhydrous sodium sulphate or SSA , natural Zeolite powder, 4A molecular sieve & laundry Zeolite powder, Linear alkyl benzene sulphonic acid or LBSA, Sodium lauryl ether sulphate or SLES , Soda ash dense and light, STPP …… if you need some new merchandises, we can also offer consulting service for you.

3.Delivery Time

-Sample Order: 1-3 days after receipt of the full payment.

-Stock Order: 3-7days after receipt of the full payment

-OEM Order: 7-12days after receipt of the deposit.

4.Payment

T/T for convenience , L/C for insurance Of course we also accept other payment ways.

5.Transportation

Transported by DHL, UPS, EMS, Air freight, sea freight etc.

6. Do you support drop shipping

Yes, your drop shipping is available.

Details:

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 Structure
 
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).

 

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