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Esfenvalerate

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CAS:66230-04-4
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CAS:66230-04-4
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CAS:66230-04-4
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Products Intro: Product Name:esfenvalerate
CAS:66230-04-4
Purity:99% Package:1kg

Esfenvalerate manufacturers

  • Esfenvalerate
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  • $41.00 / 50mg
  • 2024-11-19
  • CAS:66230-04-4
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  • 2023-07-29
  • CAS:66230-04-4
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  • $100.00 / 25KG
  • 2023-01-31
  • CAS:66230-04-4
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Esfenvalerate Basic information
Description Sources
Product Name:Esfenvalerate
Synonyms:ASANA;ASANA (TM);HALLMARK;FERTIALPHA;FORALPHA;ESFENVALERATE;Cyano-3-phenoxybenzyl (S)-2-(4-chlorophenyl)-3-methylbutyrate;AMICIDIN SUPER
CAS:66230-04-4
MF:C25H22ClNO3
MW:419.91
EINECS:613-911-9
Product Categories:Insecticide;EQ - EZMethod Specific;PesticidesPesticides;Alpha sort;E;E-GMethod Specific;Endocrine Disruptors (Draft)Alphabetic;EPA;Insecticides;Oeko-Tex Standard 100;Pesticides&Metabolites;Pyrethroids
Mol File:66230-04-4.mol
Esfenvalerate Structure
Esfenvalerate Chemical Properties
Melting point 59°C
alpha D25 -15.0° (c = 2.0 in CH3OH)
Boiling point 151-167°C
density d2323 1.163
vapor pressure 2×10-7 Pa (25 °C)
refractive index 1.6500 (estimate)
storage temp. 0-6°C
solubility DMSO : 100 mg/mL (238.15 mM; Need ultrasonic)
form Solid
Water Solubility 0.002 mg l-1 (25 °C)
color White to light yellow
BRN 4275674
LogP6.220
CAS DataBase Reference66230-04-4(CAS DataBase Reference)
NIST Chemistry ReferenceBenzeneacetic acid, 4-chloro-«alpha»-(1-methylethyl)-, cyano (3-phenoxyphenyl)methyl ester,(s-(r*,r*))-(66230-04-4)
EPA Substance Registry SystemEsfenvalerate (66230-04-4)
Safety Information
Hazard Codes T;N,N,T
Risk Statements 23/25-43-50/53
Safety Statements 24-36/37/39-45-60-61
RIDADR UN 2811
WGK Germany 3
RTECS CY1576367
HazardClass 6.1(b)
PackingGroup III
HS Code 29269090
Hazardous Substances Data66230-04-4(Hazardous Substances Data)
ToxicityLC50 (96-hour) for fathead minnows 0.69 mg/L (Worthing and Hance, 1991); acute oral LD50 for rats 75 mg/kg (Hartley and Kidd, 1987).
MSDS Information
ProviderLanguage
Esfenvalerate English
Esfenvalerate Usage And Synthesis
DescriptionEsfenvalerate is a synthetic pyrethoid insecticide – a class of pesticides originating from the chrysanthemum flower, which disrupt sodium channels. It has replaced fenvalerate, a less effective and more chronically toxic enantiomer. It can be used for general pest control, including spiders, fleas, scorpions, moths, beetles, etc. It is frequently applied on vegetable, nut, and non-crop products, often in combination with other active ingredients such as carbamate compounds and organophosphates. Product labels containing esfenvalerate include Sumi-Alpha, Hounddog, Sven, Asana, and Esfenvalerate 5EC, manufactured variously by BASF, Greencrop, and Standon.
Sourceshttp://pmep.cce.cornell.edu/profiles/extoxnet/dienochlor-glyphosate/esfenvalerate-ext.html
https://en.wikipedia.org/wiki/Esfenvalerate
https://www.domyown.com/esfenvalerate-c-114_374.html
https://en.wikipedia.org/wiki/Pyrethroid
https://www.sciencedirect.com/topics/agricultural-and-biological-sciences/esfenvalerate
https://sitem.herts.ac.uk/aeru/ppdb/en/Reports/269.htm
Chemical PropertiesViscous yellow or amber liquid or white or amber crystalline solid.
UsesEsfenvalerate is the most potent insecticidal isomer of Fenvalerate (F279450), a pyrethroid insecticide used to control insects from food crops, animal feed and cotton products.
UsesInsecticide.
UsesEsfenvalerate possesses a broad range of insecticidal activity and it is used on cotton, fruit, vegetables and other crops.
DefinitionChEBI: Esfenvalerate is a fenvalerate. It has a role as a pyrethroid ester insecticide and an agrochemical.
Agricultural UsesInsecticide: A U.S. EPA restricted Use Pesticide (RUP). Esfenvalerate is a synthetic insecticide used to control a wide range of pests such as moths, flies, beetles, and other insects. It is used on vegetable crops (soya beans, sugar cane), tree fruit, cotton, maize, sorghum and nut crops, and non-crop lands. It also is used on a wide variety of household pests. It is usually mixed with a wide variety of other types of pesticides such as carbamate compounds or organophosphates and has the naturally occurring compound fenvalerate for use in the U.S. Esfenvalerate is almost identical to fenvalerate. Much of the data for fenvalerate is applicable to the pesticide esfenvalerate because the two compounds contain the same components. The only differences in the two products are the relative proportions of the four separate constituents (isomers). Esfenvalerate has become the preferred compound because it requires lower application rates than fenvalerate, is less chronically toxic, and is a more powerful insecticide.
Trade nameAMERICARE®; ASANA®; ASANA-XL®; ASANA® DPX-YB656-84; ENFORCER®; EVERCIDE®; HALMARK®; OMS-3023®; S-1844®; S-5602 ALPHA®; SUMI-ALFA®; SUMI-ALPHA®; SS-PYDRIN®; SUMICIDIN A-ALPHA®
Potential ExposureEsfenvalerate is a synthetic pyrethroid Insecticide used to control wide range of pests such as moths, flies, beetles, and other insects. It is used on vegetable crops (soya beans, sugar cane), tree fruit, cotton, maize, sorghum and nut crops, and noncrop lands. It also isused on a wide variety of household pests. It is usually mixed with a wide variety of other types of pesticides such as carbamate compounds or organophosphates and has the naturally occurring compound fenvalerate for use in the United States Esfenvalerate is almost identical to fenvalerate. Much of the data for fenvalerate is applicable to the pesticide esfenvalerate (E:0207) because the two compounds contain the same components. The only differences in the two products are the relative proportions of the four separate constituents (isomers). Esfenvalerate has become the preferred compound because it requires lower applications rates than fenvalerate, is less chronically toxic, and is a more powerful insecticide. A United States Environmental Protection Agency Restricted Use Pesticide (RUP). Incompatibilities: Oxidizers (chlorates, nitrates, peroxides, permanganates, perchlorates, chlorine, bromine, fluorine, etc.); strong acids. Moisture may cause hydrolysis/ decomposition.
Environmental FateChemical/Physical. May hydrolyze in aqueous solutions forming acetic acid and other compounds.
Metabolic pathwayEsfenvalerate is the 2SαS-isomer of fenvalerate (which is racemic). It possesses some small differences in physical properties when compared with the racemate. Overall, the degradation and metabolism of the two compounds are very similar. Reference should be made to the fenvalerate entry. An important exception, which is discussed fully in the latter entry, is that esfenvalerate does not form the cholesterol ester conjugate that has been shown to be responsible for granulomatous changes in several tissues on repeated dosing of fenvalerate.
ShippingUN3349 Pyrethroid pesticide, solid toxic, Hazard Class: 6.1; Labels: 6.1-Poisonous material. UN3352 Pyrethroid pesticide, liquid toxic, Hazard Class: 6.1; Labels: 6.1-Poisonous materials
DegradationEsfenvalerate is hydrolysed in aqueous alkali to its constituent acid and alcohol; the latter decomposes to 3-phenoxybenzaldehyde and cyanide ion as described for fenvalerate and cypermethrin. Photodecomposition occurs as for fenvalerate.
IncompatibilitiesOxidizers (chlorates, nitrates, peroxides, permanganates, perchlorates, chlorine, bromine, fluorine, etc.); strong acids. Moisture may cause hydrolysis/ decomposition.
Waste DisposalIncineration would be an effective disposal procedure where permitted. If an efficient incinerator is not available, the product should be mixed with large amounts of combustible material and contact with the smoke should be avoided. In accordance with 40CFR165, follow recommendations for the disposal of pesticides and pesticide containers
Tag:Esfenvalerate(66230-04-4) Related Product Information
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