54406-48-3 Usage
Description
Empenthrin, an insecticidal pyrethroid compound, is a synthetic chemical derived from natural pyrethrins found in the flowers of the Chrysanthemum plant. It is characterized by its liquid chemical properties and is known for its potent insecticidal activity.
Uses
Used in Domestic Insect Control:
Empenthrin is used as a domestic insecticide for controlling moths and other insects that attack fabrics. Its effectiveness in eliminating these pests helps protect clothing and other fabric items from damage.
Used in Agricultural Applications:
Empenthrin is also utilized in the agricultural industry as an insecticide to protect crops from various insect pests. Its broad-spectrum activity makes it a valuable tool in ensuring the health and yield of crops.
Used in Veterinary Medicine:
In the veterinary field, Empenthrin is employed as an insecticide to control pests that affect the health and well-being of animals. It helps in maintaining a clean and safe environment for livestock and pets by reducing the presence of insects that may transmit diseases or cause discomfort.
Used in Public Health:
Empenthrin is also used in public health initiatives to control insect populations that transmit diseases, such as mosquitoes. Its insecticidal properties contribute to the reduction of vector-borne illnesses, thereby improving overall public health.
Metabolic pathway
Empenthrin is a low molecular weight ester of (1R)-chrysanthemic acid
(2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropanecarboxylic acid). It
has a relatively high vapour pressure and, unlike most pyrethroids, it is
effective against flying insects. The molecule has three chiral centres and
geometric isomerism in the alcohol group but, with the exception of the
1R acid, the full isomer mixture is used. As the insecticide has been
developed for domestic use, it is unlikely that there will be a requirement
for metabolism studies in plants or for extensive environmental fate studies.
Its metabolism in rats has been reported, with particular attention
paid to the fate of the novel alcohol moiety. As with other pyrethroids,
ester cleavage and oxidation and conjugation of the alcohol metabolite
predominated. The fate of the chrysanthemic acids can be assessed by
reference to phenothrin.
Degradation
Empenthrin is a stable molecule but it would be expected to be labile at
pH values above 10.
Check Digit Verification of cas no
The CAS Registry Mumber 54406-48-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,4,0 and 6 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 54406-48:
(7*5)+(6*4)+(5*4)+(4*0)+(3*6)+(2*4)+(1*8)=113
113 % 10 = 3
So 54406-48-3 is a valid CAS Registry Number.
InChI:InChI=1/C18H26O2/c1-8-10-13(5)15(9-2)20-17(19)16-14(11-12(3)4)18(16,6)7/h2,10-11,14-16H,8H2,1,3-7H3
