23505-41-1 Usage
Uses
Used in Agriculture:
Pirimiphos ethyl is used as an insecticide for the protection of crops. It is effective against a wide range of pests, including aphids, whiteflies, and mites, which can cause significant damage to plants and reduce crop yields. By controlling these pests, pirimiphos ethyl helps to maintain the health and productivity of crops.
Used in Public Health:
In addition to its agricultural applications, pirimiphos ethyl is also used in public health settings to control pests that can transmit diseases. It is particularly useful in combating mosquitoes, which are known vectors for diseases such as malaria, dengue fever, and Zika virus. By reducing mosquito populations, pirimiphos ethyl can play a crucial role in disease prevention and control efforts.
Used in Stored Product Protection:
Pirimiphos ethyl is also used to protect stored products, such as grains and cereals, from infestation by pests like beetles and weevils. These pests can cause significant economic losses by damaging stored goods, and the use of pirimiphos ethyl helps to prevent such losses and maintain the quality of stored products.
Used in Veterinary Medicine:
In veterinary medicine, pirimiphos ethyl is used to control ectoparasites, such as ticks and mites, that can infest livestock. These parasites can cause discomfort to animals and may also transmit diseases. By using pirimiphos ethyl to control these pests, it helps to ensure the health and well-being of animals in the livestock industry.
Reactivity Profile
Organophosphates, such as Pirimiphos ethyl, are susceptible to formation of highly toxic and flammable phosphine gas in the presence of strong reducing agents such as hydrides. Partial oxidation by oxidizing agents may result in the release of toxic phosphorus oxides.
Health Hazard
Pirimiphos ethyl is an organophosphorus pesticide and is absorbed by the skin, as well as by the respiratory and gastrointestinal tracts. It is a cholinesterase inhibitor, acting on the nervous system.
Fire Hazard
As with other organophosphorus pesticides, container may explode in heat of fire. Heat may cause decomposition and evolution of highly toxic fumes of phosphorus oxides, nitrogen oxides and sulfur oxides. Decomposes above 266F.
Potential Exposure
A potential danger to those involved in the manufacture, formulation and application of this organophosphate soil insecticide.
Shipping
In accordance with 40CFR165, follow recommendations for the disposal of pesticides and pesticide containers. Must be disposed properly by following package label directions or by contacting your local or federal environmental control agency, or by contacting your regional EPA office.
Check Digit Verification of cas no
The CAS Registry Mumber 23505-41-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,5,0 and 5 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 23505-41:
(7*2)+(6*3)+(5*5)+(4*0)+(3*5)+(2*4)+(1*1)=81
81 % 10 = 1
So 23505-41-1 is a valid CAS Registry Number.
InChI:InChI=1/C13H24N3O3PS/c1-6-16(7-2)13-14-11(5)10-12(15-13)19-20(21,17-8-3)18-9-4/h10H,6-9H2,1-5H3
23505-41-1Relevant articles and documents
Liquid formulations
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, (2008/06/13)
A pour-on formulation comprising one or more ectoparasiticides in a solvent system comprising 80 to 98% w/v of a fixed oil and 2 to 20% w/v of a volatile silicone, a method for its preparations and its use in the control of ectoparasiticides on animals.
Acetic acid derivatives and processes for their production
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, (2008/06/13)
A process for the preparation of a compound of formula: STR1 wherein R is an amino, hydrocarbylamino or dihydrocarbylamino radical, the hydrocarbylamino and dihydrocarbylamino radicals being unsubstituted, or substituted in the hydrocarbyl moiety with atoms or radicals which do not interfere with the process and Z is an acyl radical which comprises the steps of: (a) decarboxylating a compound of formula: STR2 to produce the corresponding 4-hydroxy-6-methyl-pyrimidine; and (B) TREATING THE CORRESPONDING 4-HYDROXY-6-METHYL PYRIMIDINE THUS PRODUCED WITH AN ACYLATING AGENT CAPABLE OF PROVIDING THE ACYL RADICAL Z; where both steps (a) and (b) are carried out in the same solvent or diluent.
