28434-00-6 Usage
Description
S-Bioallethrin, a synthetic insecticide structurally similar to pyrethrin, is a potent constituent of allethrin. It is a clear to amber viscous liquid and a yellow liquid that is miscible with most organic solvents. As an ester of the (1R, trans)-acid with (1S)-allethrolone, S-Bioallethrin exhibits fast knock-down activity against household pest insects, making it several times more effective than allethrin.
Uses
Used in Insecticides:
S-Bioallethrin is used as a contact insecticide for its rapid knockdown effect against flying and crawling insects. Its effectiveness is further enhanced by the addition of a synergist such as piperonyl butoxide or MGK 264 in pesticide formulations.
Used in Public Health Applications:
S-Bioallethrin is employed in public health applications to control mosquitoes, houseflies, and cockroaches. It is particularly useful in indoor settings, where it can be applied in aerosols, coils, or sprays to combat these pests effectively.
Used in Household Pest Control:
S-Bioallethrin is utilized in various household pest control products, such as aerosols, coils, and sprays, to target and eliminate flying and crawling insects, contributing to a cleaner and healthier living environment.
Air & Water Reactions
Insoluble in water.
Reactivity Profile
ALLETHRIN is incompatible with alkalis.
Check Digit Verification of cas no
The CAS Registry Mumber 28434-00-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,4,3 and 4 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 28434-00:
(7*2)+(6*8)+(5*4)+(4*3)+(3*4)+(2*0)+(1*0)=106
106 % 10 = 6
So 28434-00-6 is a valid CAS Registry Number.
InChI:InChI=1/C19H26O3/c1-7-8-13-12(4)16(10-15(13)20)22-18(21)17-14(9-11(2)3)19(17,5)6/h7,9,14,16-17H,1,8,10H2,2-6H3/t14-,16-,17+/m1/s1
28434-00-6Relevant articles and documents
Process for producing cyclopropanecarboxylates
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, (2008/06/13)
There is disclosed a process process for producing a cyclopropanecarboxylate of formula (1): 1which process comprises reacting cyclopropanecarboxylic acid of formula (2): 2with a monohydroxy compound of formula (3): R6OH??(3),in the presence of a catalyst compound comprising an element of to Group 4 of the Periodic Table of Elements.