US2014120186A1PendingUtilityA1
Insecticidal compositions and methods of using the same
Assignee: CLARKE MOSQUITO CONTROL PRODUCTS INCPriority: Jul 13, 2011Filed: Jan 7, 2014Published: May 1, 2014
Est. expiryJul 13, 2031(~4.9 yrs left)· nominal 20-yr term from priority
Inventors:Michael Dean WillisMarie Elizabeth SaundersDarryl RamoutarJoanna Maria SzymczykFrances Nita KrenickAndrea Rohrbacher
A01N 65/22A01N 37/06A01N 65/00A01N 53/00A01N 31/06A01N 35/02A01N 43/56A01N 35/06A01N 27/00A01N 49/00Y02A50/30
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Claims
Abstract
Insecticidal compositions have at least one active agent and at least one insecticide. The active agent can include perilla oil, a component found in perilla oil, or a perillaldehyde or carvone analog. The insecticide can include a pyrethrum, pyrethrin, pyrethroid, neonicotinoid, chlofenapyr, ethiprole, sulfoxoflor, carbamate, organophosphate, or organochlorine. Methods for controlling insects include contacting an insect with an effective amount of a composition described in this specification. Modified plants that produce an active agent can be contacted with an insecticide.
Claims
exact text as granted — not AI-modifiedWhat is claimed is:
1 . An insecticidal composition comprising an insecticide and an active agent present in an amount of about 1% to 99% by weight of the composition, the active agent selected from the group consisting of (i) perilla oil; (ii) a perilla oil component selected from the group consisting of farnesene, perillaldehyde, linolenic acid, caryophyllene, limonene, carvone, perillyl alcohol, perillic acid, pinene, linalool, germacrene, bergamotene, and spathulenol; and (iii) a perillaldehyde analog.
2 . The composition of claim 1 , wherein the active agent comprises perilla oil, perillaldehyde, or carvone, including (R)-carvone or (S)-carvone.
3 . The composition of claim 1 , wherein the perillaldehyde analog is a compound of formula (A):
wherein:
R 1 is selected from the group consisting of —CH 2 OH, —CHO, and —COOR a ;
R 2 is selected from the group consisting of hydrogen, alkyl and alkenyl;
R 3 is selected from the group consisting of hydrogen and alkyl;
R 4 is hydrogen, or R 4 and R 2 are taken together with the atoms to which they are attached to form an optionally substituted ring; and
R a is selected from the group consisting of hydrogen and alkyl.
4 . The composition of claim 1 , wherein the perillaldehyde analog is selected from the group consisting of limonene including D-limonene, perillyl alcohol including (S)-(−)-perillyl alcohol, perillic acid including (S)-(−)-perillic acid, myrtenal including (1R)-(−)-myrtenal, and 3-methyl-1-cyclohexene-1-carboxaldehyde.
5 . The composition of claim 1 , wherein the insecticide is selected from the group consisting of pyrethrin, pyrethroid, neonicotinoid, chlofenapyr, ethiprole, sulfoxoflor, carbamates, organophosphates, and organochlorines.
6 . The composition of claim 5 , wherein the insecticide comprises one or more naturally occurring pyrethrins selected from the group consisting of Jasomolin-I, Cinerin-I, Pyrethrin-I, Jasmolin-II, Cinerin-II, and Pyrethrin-II.
7 . The composition of claim 5 , wherein the insecticide comprises one or more pyrethroids selected from the group consisting of etofenprox, permethrin, prallethrin, resmethrin, and sumithrin.
8 . The composition of claim 5 , wherein the insecticide comprises one or more compounds selected from the group consisting of allethrin, alpha-cypermethrin, bifenthrin, beta-cypermethrin, cyfluthrin, cypermethrin, deltamethrin, esfenvalerate, etofenprox, lamdba-cyhalothrin, and zeta-cypermethrin.
9 . The composition of claim 5 , wherein the insecticide comprises one or more neonicotinoids selected from the group consisting of dinotefuran, acetamiprid, clothianidin, imidacloprid, nitenpyram, thiacloprid, and thiamethoxam.
10 . The composition of claim 9 , wherein the insecticide comprises at least one of clothianidin or imidacloprid.
11 . The composition of claim 1 , wherein the composition is substantially free of piperonyl butoxide.
12 . The composition of claim 1 , wherein the composition is substantially free of N-octyl bicycloheptene dicarboximide.
13 . The composition of claim 1 , wherein the composition comprises less than about 95% by weight of the insecticide.
14 . The composition of claim 1 , wherein the composition comprises less than about 60% by weight of the insecticide.
15 . The composition of claim 1 , wherein the composition further comprises mineral oil, glycerol, or other diluent that provides viscosity modifying properties.
16 . The composition of claim 1 , wherein the composition is suitable for application as at least one of an aerosol, fog, mist, spray, ultra low volume spray, or surface contact treatment.
17 . A method for controlling insects, the method comprising contacting a population of insects with an effective amount of the composition of claim 1 .
18 . The method of claim 17 , wherein the insect is a mosquito.
19 . The method of claim 17 , wherein the composition is topically applied to the population in an amount sufficient to kill at least 25% of the population.
20 . The method of claim 17 , wherein the composition is topically applied to the population in an amount sufficient to kill at least 50% of the population.
21 . The method of claim 17 , wherein the composition is applied by at least one of an aerosol, mist, fog, spray, vapor, ULV spray, or surface contact treatment.
22 . The method of claim 17 , wherein the population is exposed to the insecticide so that the composition is ingested by the insects sufficient to kill at least 50% of the population.Join the waitlist — get patent alerts
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