WO2018217554A1 - Ternary insecticidal composition - Google Patents
Ternary insecticidal composition Download PDFInfo
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- WO2018217554A1 WO2018217554A1 PCT/US2018/033322 US2018033322W WO2018217554A1 WO 2018217554 A1 WO2018217554 A1 WO 2018217554A1 US 2018033322 W US2018033322 W US 2018033322W WO 2018217554 A1 WO2018217554 A1 WO 2018217554A1
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- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N53/00—Biocides, pest repellants or attractants, or plant growth regulators containing cyclopropane carboxylic acids or derivatives thereof
Definitions
- the present disclosure relates to a composite insecticidal composition and, more particularly, to an aerosol composite insecticidal composition, that comprises at least three active ingredients and is effective against both flying and crawling insects.
- Insecticide has been used over the years to prevent insects from attacking humans, animals, and crops. Diseases transmitted by insects are a major health hazard. Insects (mosquitoes, flies, and the like) transmit a number of diseases caused by the exposure of the victim to infectious agents such as viruses (chikungunya virus, yellow fever, dengue fever, etc.), bacteria (Lyme disease, plague, etc.), and parasites (malaria, sleeping sickness, leishmaniasis, filariasis, etc.) carried by the insect.
- viruses chikungunya virus, yellow fever, dengue fever, etc.
- bacteria Lyme disease, plague, etc.
- parasites malaria, sleeping sickness, leishmaniasis, filariasis, etc.
- mosquitoes cause greater human suffering than any other organism— over one million people worldwide die from mosquito-borne diseases annually.
- mosquitoes carry diseases that afflict humans, they also transmit several diseases and parasites that affect other animals, such as dogs and horses. These include dog heartworm, West Nile virus (WNV), and Eastern equine encephalitis (EEE).
- WNV West Nile virus
- EEE Eastern equine encephalitis
- mosquito bites may cause severe skin irritation resulting from an allergic reaction to the mosquito's saliva, causing inflammation and itching at the affected site, leading to the possible introduction of other disease causing agents.
- Crawling insects such as ants and cockroaches, are responsible for health problems as well.
- Cockroaches in the home environment are a health hazard not only because of the risks posed by cockroach antigens to asthma sufferers, but also because they can carry disease-causing agents. Cockroaches may play a role as carriers of intestinal diseases, such as diarrhea, dysentery, typhoid fever and cholera.
- Known commercially available insecticides are typically effective against either flying insects or crawling insects, but not both. Therefore, it is desirable to have a composite insecticidal composition with the ability to knockdown and kill both flying and crawling insects in a quick, efficient manner, be available in a single product, and to further provide residual activity.
- Embodiments of the current disclosure describe a composite insecticidal composition comprising transfluthrin, prallethrin, and cypermethrin.
- the transfluthrin is present at about 0.05% to about 0.5% by weight; the prallethrin at about 0.05% to about 0.5% by weight; and the cypermethrin at about 0.05% to about 0.5% by weight.
- the transfluthrin is present at about 0.1% by weight; the prallethrin at about 0.1% by weight; and the cypermethrin at about 0.1% by weight.
- the composite insecticidal composition further comprises at least one of a solvent and a propellant.
- the solvent may comprise aliphatic C9-C14 hydrocarbons, alicyclic C9-C14 hydrocarbons, naphtha, petroleum distillate, paraffins, iso-paraffins,
- the propellant may comprise methane, ethane, propane, pentane, isobutene, N-butane, iso-butane, dimethyl ether, 1, 1-difluoroethane, 1,1, 1,2-tetrafluoroethane, carbon dioxide, nitrogen, air, and the like, and any combinations thereof.
- the composite insecticidal composition is a composition for killing insects, comprising between about 0.05 and 0.5% by weight of transfluthrin, between about 0.05 and 0.5% by weight of prallethrin, between about 0.05 and 0.5% by weight of cypermethrin, between about 10 and 90% by weight of a petroleum distillate solvent or an isoparaffinic hydrocarbon solvent or both, and between about 10 and 80% by weight of a propellant.
- Certain embodiments comprise a method of killing insects, the method comprising providing the composition of claim 1 in a dispenser which dispenses the composition at a rate of between about 2.0 gram/second and about 3.5 gram/second, and instructing a user to spray the composition for a duration of between about 4 and about 5 seconds.
- a composite insecticidal composition designed to knockdown and kill both flying and crawling insects more effectively than other known compositions is presently disclosed.
- households tend to suffer from both flying and crawling insects. Therefore, it is important to develop an insecticidal composition that can knockdown and/or kill both flying and crawling insects in a timely fashion. It has been found that an insecticidal composition comprising three actives may provide such a benefit.
- the composite insecticidal composition comprises transfluthrin, prallethrin, and cypermethrin.
- Transfluthrin is a fast-acting pyrethroid insecticide with low persistency. It has the molecular formula C15H12CI2F4O2.
- Prallethrin is another pyrethroid insecticide, which has the molecular formula C19H24O3.
- Cypermethrin is a synthetic pyrethroid used as an insecticide in large-scale commercial agricultural applications as well as in consumer products for domestic purposes. It behaves as a fast-acting neurotoxin in insects. It is easily degraded in soil and on plants but can be effective for weeks when applied to indoor inert surfaces, providing long residual activity.
- Cypermethrin has a molecular formula of C22H19CI2NO3.
- the type of active ingredients, the spray rate of the composition, and the instructions regarding use of the composition are considered.
- the spray rate of the active ingredients is in the range of about 2.0 grams per second to about 2.5 grams per second.
- the spray rate of the active ingredients is in the range of about 2.5 grams per second to about 3.0 grams per second.
- the spray rate of the active ingredients is in the range of about 3.0 grams per second to about 3.5 grams per second.
- the user instructions for aerosol compositions may instruct the user to spray for about 4 to about 5 seconds.
- users are instructed to spray for about 5 to about 8 seconds. In yet other embodiments, users are instructed to spray for about 8 to about 12 seconds. It is desirable to provide an insecticidal composition comprising a particular amount of active ingredient to reach its best efficacy (ability to kill or knock down pests) when a certain spray rate and a certain amount of spray time (spray duration) are used.
- the transfluthrin is about 0.05% to about 0.5% by weight
- the prallethrin is about 0.05% to about 0.5% by weight
- the cypermethrin is about 0.05% to about 0.5% by weight.
- the transfluthrin is about 0.1% by weight
- the prallethrin is about 0.1% by weight
- the cypermethrin is about 0.1% by weight.
- the particular weight percentage may vary, but each of the transfluthrin, prallethrin, and cypermethrin are equal in their particular weight percentage to one another.
- the weight percentage of each component is at least about 0.1%), or less than or equal to about 0.5%, or greater than or equal to about 0.05%.
- concentrations of all the active ingredients may vary to suit different applications.
- concentration ranges of active ingredients are associated not only with the type of active ingredient, but with spray rate and instructions for use, including, but not limited to, spray duration and/or recommended proximity to the pest.
- Peet-Grady chambers were used in the studies conducted on mosquitoes and also on Periplaneta americana and Blatella germanica cockroaches. About 2.5 to about 3.5 grams of each test substance was sprayed into the chamber and mortality was observed 60 minutes after spraying of the test substances. In the first 10 minutes of observing the mortality, the number of falling mosquitoes or cockroaches was recorded at one minute intervals. After the first 10 minutes, the number of falling mosquitoes or cockroaches was recorded at 10 minute intervals up until 60 minutes. Following the first 60 minutes of the mortality observation, all the tested mosquitoes were moved outside the chambers and placed in a room. The number of falling mosquitoes was recorded every hour until the sixth hour. After 24 hours of observation, the number of mosquitoes that can revive and become active again was also recorded. Similarly, the number of falling cockroaches was recorded every hour until the sixth hour and at 24 hours. Studies were conducted at two testing locations.
- Composition 1 according to an embodiment of the present disclosure comprises about 0.1% by weight cypermethrin, about 0.1% by weight transfluthrin, about 0.1% by weight prallethrin, about 29% to about 29.7% by weight isoparaffinic hydrocarbon solvent and about 70% by weight propellant.
- the average knockdown of Culex quinquefasciatus (southern house mosquito) after exposure to Composition 1 for 1 minute is about 3.5%, for 2 minutes about 21%, for 3 minutes about 38.5%), for 4 minutes about 54%, for 5 minutes about 67%, for 6 minutes about 79.5%, for 7 minutes about 86.5%, for 8 minutes about 93%, and for 9 minutes about 98%.
- Exposure to Composition 1 reaches about 100% knockdown of the southern house mosquito in about 10 minutes, which is significantly faster in comparison to other known compositions. Further, Composition 1 has a faster and higher knockdown rate of the southern house mosquito over any other tested formulations, except for Formula 1. After 24 hours exposure to Composition 1, about 99.5%) of the southern house mosquitoes were killed.
- a "dead” (or killed) insect must be an insect with absolutely no movement, no twitching, no antenna moving, etc.
- a dead insect is probed or subjected to other stimuli to verify lack of movement.
- a "knockdown" of an insect is considered to be any condition between dead and full mobility, i.e., knockdown is often measured as the insect's inability to respond to a stimulus such as light or touch.
- knockdown is defined as mosquitoes resting on the floor of the chamber and experiencing some aberrant behavior, such as on laying on their back or side, spinning erratically in one spot, or the inability to sustain normal flight more than a few inches giving an impression of hopping.
- knockdown is used to measure the effect of a pesticide. It is desirable to not only knockdown, but to kill insects to avoid the breeding of knockdown resistant insects.
- Knockdown resistance (“kdr"), describes cases of resistance to diphenyl ethane (e.g. DDT) and pyrethroid insecticides in insects and other arthropods that result from reduced sensitivity of the nervous system caused by point mutations in the insect's genetic makeup. Such mutative resistance is characterized by the presence of kdr alleles in the insect's genome. Knockdown resistance remains a threat to the continued usefulness of pyrethroids in the control of many pest species.
- the average knockdown of southern house mosquitoes after exposure to Composition 1 for 1 minute is about 9.3%, for 2 minutes about 20.7%, for 3 minutes about 36.7%, for 4 minutes about 47.3%o, for 5 minutes about 63.3%>, for 6 minutes about 76.7%, for 7 minutes about 78%, for 8 minutes about 86.7%, for 9 minutes about 90%, and for 12 minutes about 98.7%.
- Exposure to Composition 1 reaches 100% knockdown of the southern house mosquito in about 13 minutes, significantly faster in comparison to other known compositions. After 24 hours exposure to Composition 1, 100%) of the southern house mosquitoes were killed.
- Composition 1 has a faster and higher knockdown rate of the southern house mosquito than any other tested formulations.
- the average of knockdown of Aedes aegypti (yellow fever mosquito) after exposure to Composition 1 for 1 minute is about 77% and for 2 minutes about 93%.
- Exposure to Composition 1 reaches 100% knockdown of the yellow fever mosquito in just 3 minutes, significantly faster in comparison to other known compositions.
- Composition 1 has a faster and higher knockdown rate of the yellow fever mosquitos than any other tested formulation.
- Composition 1 is also effective against crawling insects, such as Periplantea americana (American cockroach) and Blatella germanica (German cockroach). The average knockdown of American cockroaches following space spray exposure to crawling insects, such as Periplantea americana (American cockroach) and Blatella germanica (German cockroach). The average knockdown of American cockroaches following space spray exposure to crawling insects, such as Periplantea americana (American cockroach) and Blatella germanica (German cockroach). The average knockdown of American cockroaches following space spray exposure to
- Composition 1 for 1 minute is about 4%, for 2 minutes about 27.2%, for 3 minutes about 40%, for 4 minutes about 77.6%, for 5 minutes about 88%, for 6 minutes about 92.8%, for 7 minutes about 94.4%), for 8 minutes about 95.2%, and for 9 minutes about 96%.
- Exposure to Composition 1 reaches 100% knockdown of American cockroaches in about 10 minutes, which is significantly faster in comparison to other known compositions.
- After 24 hours exposure to Composition 1, about 20.8%) of American cockroaches were killed.
- the average knockdown of German cockroaches following space spray exposure to Composition 1 for 1 minute is about 89.6% and reaches about 100% in 2 minutes.
- Composition 1 for 1 minute is about 59%, for 2 minutes about 84%, for 3 minutes about 96%, and reaches 100% in just about 4 minutes.
- Composition 1 has a faster and higher knockdown rate of American cockroaches than any other tested formulation.
- the average knockdown of German cockroaches after direct spray exposure to Composition 1 for 1 minute is about 72%, for 2 minutes about 44%, and reaches 100% in about 3 minutes.
- Composition 1 has a faster and higher knockdown rate of German cockroaches than any other tested formulation.
- the currently disclosed composite insecticidal composition exhibits faster and higher knockdown rates and higher killing rates against flying insects and crawling insects compared to other tested formulations.
- Other formulations including other commercially available formulations, may have only fast and high knockdown rates against either flying insects or crawling insects, but not both.
- the currently disclosed composite insecticidal composition is the only composition known that is effective against both flying and crawling insects at the rates and times disclosed herein. Table 1 provides a comparative study with other tested insecticidal formulations. All Peet-
- Grady Data is generated from label usage dosage of 1.8 seconds except for Composition 1 (0.90 second dose), and all direct spray knockdown data is generated using a 1.0 second dose from 18 inches unless noted with an asterisk (*).
- Formulation D Mean Aedes aegypti mean Mean KT90 Mean KT90 100% KD at KT90 KT90 11.74 min 10.08 sec 62.10 sec 5 min
- Formulation E Mean Aedes aegypti mean Mean KT90 Mean KT90 100% KD at
- Prallethrin Anopheles mean KT90
- Formulation F Mean Aedes aegypti mean 92% KD at 5 84% KD at 5 100% KD at
- Prallethrin Anopheles mean KT90
- Formulation G Mean Aedes aegypti mean Mean KT90 Mean KT90 NA
- d-Phenothrin Anopheles mean KT90
- Formulation H Mean Aedes aegypti mean Mean KT90 92% KD at 100% KD at
- quinquefasciatus, Anopheles stephensi, and Aedes albopictus) is generated using a Peet-Grady test chamber.
- the test substance, Composition 1 was sprayed into the Peet-Grady test chamber for about 0.9 seconds in the presence of adult mosquitos and houseflies.
- the other test substances, such as Formulations A-H were sprayed into the Peet-Grady test chamber for about 1.8 seconds in the presence of adult mosquitos and houseflies.
- the methodology provides a comparison using 0.9 seconds vs 1.8 seconds to demonstrate that Composition 1 in a 50% spray duration (0.9 seconds) performs better than the comparative formulations having a spray duration of 1.8 seconds. In other words, Composition 1 outperformed the comparative formulations, using only 50% of the spray duration of the comparative formulations.
- a container holding a testing substance was weighed after spraying and the difference was calculated (D) and the contents of the container were discharged into the spray hood for 5 seconds (S).
- Mosquitoes were introduced to the testing chamber and were acclimated for
- the container including the test substances Prior to the treatment, the container including the test substances were weighed. The container was re-weighed after treatment. The weight of the test substances was measured after spraying to determine the actual dosage. Following mosquito acclimation, the test substances were sprayed into the chamber for about 0.9 seconds (Composition 1) or about 1.8 seconds (Formulations A-H). Immediately following the application the testing chamber was closed and the timer started. Knockdown counts were taken beginning approximately 30 seconds before the actual 3, 5, and 10-minute intervals. At approximately 14 minutes an exhaust on the chamber was opened. At approximately 15 minutes the downed mosquitoes were counted. To obtain a total mosquito count, the mosquitoes that were not knocked down were then collected and counted.
- Knockdown counts were taken at 15 minutes and 24-hour mortality counts at 24 ⁇ 2 hours.
- the average time to reach 90% mortality (KT90) in houseflies when using Composition 1 was about 5.38 minutes, which is shorter than most KT90 of Formulations A-H, even though the spray durations of Formulations A-H were twice that of Composition 1.
- the KT90 of each of the four different types of mosquitoes when using Composition 1 was much lower than the KT90 of each of Formulations A-H respectively, also with a spray duration twice that of Composition 1.
- the composite insecticidal composition further comprises at least one of a solvent and a propellant.
- the composite insecticidal composition may further comprise a fragrance. Such embodiments may comprise a fragrance at about 0.1% to about 2% by weight.
- the composite insecticidal composition is an aerosol insecticidal composition, which is suitable for industrial and domestic applications.
- An embodiment comprises a dispensing container having aerosol dispensing means, at least three active ingredients, a solvent at a sufficient weight percentage to dissolve the active ingredients, and a propellant gas at a sufficient pressure to dispense the active ingredients dissolved in the solvent from the dispensing means as an aerosol.
- An aerosol insecticidal composition is ideal for use against both flying and crawling insects.
- the aerosol composition may be sprayed in the air for any flying insect and may be sprayed in the air for preventative measures.
- crawling insects the aerosol composition may be sprayed directly on the insect or on inert surfaces such as, but not limited to, floorboards, under the sink, thresholds, and doorways as a preventative measure.
- the solvent may be aliphatic C9-C14 hydrocarbons, alicyclic C9- Ci4 hydrocarbons, naphtha, petroleum distillate, paraffins, iso-paraffins, isoparaffinic
- the solvent is a petroleum distillate.
- the petroleum distillate is comprised of hydrocarbons, C11-C14, n-alkanes, isoalkanes, cyclics, ⁇ 2% aromatics.
- the solvent is an isoparaffinic hydrocarbon.
- the isoparaffinic hydrocarbon is naphtha (petroleum), hydrotreated heavy.
- the solvent is comprised of a petroleum distillate or an isoparaffinic hydrocarbon or both. Certain embodiments may comprise at least two solvents.
- the molar ratio of the at least two solvents may be in the range of about 1 : 1 to about 1 : 100 or about 1 : 100 to about 1 : 1 based on the total concentration of the solvents.
- the solvent is present at an appropriate amount to dissolve the active ingredients, and may also contribute to carrier efficiency, which is defined as the degree to which a solvent induces penetration of an insecticide into the pest.
- Petroleum distillates are commonly used to refer to aliphatic hydrocarbons, defined to also include natural or synthetic paraffinic hydrocarbons. Petroleum distillates may include mineral spirits, kerosene, white spirits, naphtha, Stoddard solvents, and the like. These products may contain trace amounts of benzene and/or other aromatics.
- solvents such as butylglycol, carbon tetrachloride, chloroform, chloropenthane, cresol, cyclohexanol, cyclohexanone, dibromom ethane, 1,2- dichlorobenzene, 1,1-dichloroethane, 1,2-dichloroethane, dichloroethylene, 1,1-dichloroethylene, 1,2-dichloropropane, diethylbenzene, dimethyl carbonate, ⁇ , ⁇ -dimethylformamide, 1,4-dioxane, ethylbenzene, ethylene glycol, ethylglycol, formol, furfuryl alcohol, isophorone, isopropyl glycol, kerosene, mesithyl oxide, mesithylene, methanol, 2-methoxypropanol, methylmetacrylate, methylcyclohexan
- Certain solvents can increase the rate of penetration of contact insecticides through the insect cuticle.
- the solvent is present at about 10% to about 90% by weight, preferably, about 25% to about 35% by weight. In a preferred embodiment, the solvent is present in about 30% by weight. While specific values of the solvent are chosen for this embodiment, it is to be understood that, within the scope of the disclosure, this value may vary over wide ranges to suit different applications.
- the weight percentage of the solvent may increase to dissolve the active ingredients when, for example, there are additional active ingredients in one composition formula compared to another. The weight percentage of the solvent is balanced to effectively dissolve the active ingredients and effectively penetrate the cuticles of insects.
- the propellant pressurizes the aerosol container and influences the form in which the composite insecticidal composition is discharged.
- the composition may be discharged in the form of foam, stream, or spray.
- the pressure normally created by the propellant is about 0.7 to about 9.8 bars (35 psi to 140 psi) at 21.1 °C. If propellant concentration is increased, the composition may be discharged in the form of lower density foams.
- the propellant By adjusting the propellant and solvent used, quick breaking foams can be produced, or foams can be created that remain visually unchanged for days.
- the propellant must have sufficient dispersive energy to overcome the surface tension of the liquid mixture, plus the cohesive and adhesive forces.
- Aerosol propellants may comprise compressed gases, soluble gases, and liquefied gases.
- the propellant may be carbon dioxide, nitrogen, air, and the like, or any combinations thereof.
- the propellant belongs to the liquefied gases category including, but not limited to hydrocarbon propellants.
- the propellant may be methane, ethane, propane, pentane, isobutene, N-butane, iso-butane, dimethyl ether, 1, 1-difluoroethane, 1, 1,1,2-tetrafluoroethane and the like, and any combinations of two or more thereof.
- the propellant is propane.
- the propellant is butane, including both N-butane and iso-butane.
- Some embodiments may comprise at least a first propellant and a second propellant.
- the first and second propellants are in a molar ratio in the range of about 1 : 1 to about 100: 1, or about 100: 1 to about 1 : 1 based on the total concentration of the first and second propellant.
- the first propellant is propane and the second propellant is butane.
- the propellant is present in about 0.5% to about 90% by weight, more preferably, about 10% to about 80% by weight. In a preferred embodiment, the propellant is present in about 70% by weight. While specific values chosen for the propellant are recited, it is to be understood that, within the scope of the disclosure, the value of this parameter may vary over wide ranges to suit different applications.
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Abstract
Description
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Priority Applications (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| BR112019024465-4A BR112019024465B1 (en) | 2017-05-22 | 2018-05-18 | COMPOSITIONS COMPRISING TRANSFLUTHrin, PRALETHRIN AND CYPERMETHRIN AND USE THEREOF FOR THE EXTERMINATION OF INSECTS |
| MX2019014032A MX2019014032A (en) | 2017-05-22 | 2018-05-18 | Ternary insecticidal composition. |
| PH12019502604A PH12019502604A1 (en) | 2017-05-22 | 2019-11-20 | Composite insecticidal composition |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US15/601,393 | 2017-05-22 | ||
| US15/601,393 US10405552B2 (en) | 2017-05-22 | 2017-05-22 | Composite insecticidal composition |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| WO2018217554A1 true WO2018217554A1 (en) | 2018-11-29 |
Family
ID=62620960
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/US2018/033322 Ceased WO2018217554A1 (en) | 2017-05-22 | 2018-05-18 | Ternary insecticidal composition |
Country Status (5)
| Country | Link |
|---|---|
| US (2) | US10405552B2 (en) |
| AR (1) | AR111821A1 (en) |
| MX (1) | MX2019014032A (en) |
| PH (1) | PH12019502604A1 (en) |
| WO (1) | WO2018217554A1 (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2025016887A1 (en) | 2023-07-14 | 2025-01-23 | Reckitt & Colman (Overseas) Hygiene Home Limited | Pest control composition |
| WO2026046842A1 (en) | 2024-08-26 | 2026-03-05 | Reckitt & Colman (Overseas) Hygiene Home Limited | Pest control composition |
Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5091183A (en) * | 1989-09-14 | 1992-02-25 | Sumitomo Chemical Company, Limited | Insecticidal and/or acaricidal composition |
| WO2014040720A1 (en) * | 2012-09-14 | 2014-03-20 | Aragon Net Ltd. | Insecticidal aerosol |
| CN104522040A (en) * | 2014-12-24 | 2015-04-22 | 东莞市绿雅达有害生物防制技术有限公司 | Invertebrate pest control agent mixture and preparation method thereof |
| WO2015159772A1 (en) * | 2014-04-18 | 2015-10-22 | 大日本除蟲菊株式会社 | Mosquito control aerosol and mosquito control method |
Family Cites Families (49)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0125471A3 (en) | 1983-04-07 | 1986-09-17 | The Wellcome Foundation Limited | Pesticidal composition |
| AU605652B2 (en) | 1987-12-15 | 1991-01-17 | Sumitomo Chemical Company, Limited | Insecticidal aerosol |
| AU611590B2 (en) | 1988-11-11 | 1991-06-13 | Sumitomo Chemical Company, Limited | Insecticidal composition comprising 2,4-dioxo-1-(2- propynyl)imidazolidin-3-ylmethyl chrysanthemate, organic solvent and kerosine, and an aerosol containing same |
| HU204393B (en) | 1988-12-22 | 1992-01-28 | Chinoin Gyogyszer Es Vegyeszet | Insecticide aqouos solutions containing piretroides as active components and microemulsion compositions containing former solutions |
| EP1070752A3 (en) | 1990-09-03 | 2003-08-27 | Connetics Australia Pty Limited | A concentrated aerosol space spray |
| FR2713235B1 (en) | 1993-11-29 | 1996-01-19 | Rhone Poulenc Agrochimie | Composition for aerosol and aerosol generating system containing it. |
| ZA96514B (en) | 1995-01-27 | 1996-08-13 | Johnson & Son Inc S C | Insecticidally-active composition |
| US6582714B1 (en) | 1995-04-10 | 2003-06-24 | S. C. Johnson & Son, Inc. | Article for insert control by passive evaporation of an active ingredient |
| DE69625499T2 (en) | 1995-06-22 | 2003-07-24 | Reckitt Benckiser (Australia) Pty Ltd., West Ryde | INSECTICIDE AEROSOL SPRAY COMPOSITIONS |
| GB9520705D0 (en) | 1995-10-10 | 1995-12-13 | R & C Products Pty Ltd | Improvements in or relating to organic compounds |
| AU722204B2 (en) | 1995-10-31 | 2000-07-27 | Sumitomo Chemical Company, Limited | Pesticidal composition |
| DE69618620D1 (en) | 1996-06-11 | 2002-02-21 | Attavet Aubagne | INSECTICIDAL AND ANTIPARASITARY AQUEOUS COMPOSITION, METHOD FOR THEIR PRODUCTION AND USE |
| US5792465A (en) | 1996-06-28 | 1998-08-11 | S. C. Johnson & Son, Inc. | Microemulsion insect control compositions containing phenol |
| JP3855311B2 (en) | 1996-08-07 | 2006-12-06 | 住友化学株式会社 | Aerosol composition |
| US6028117A (en) | 1996-12-18 | 2000-02-22 | S. C. Johnson & Son, Inc. | Microemulsion insect control compositions |
| US5912003A (en) | 1997-02-12 | 1999-06-15 | Kukbo Pharma Co., Ltd. | Spray-type insecticidal paint and manufacturing process thereof |
| GB2327881A (en) | 1997-08-06 | 1999-02-10 | Reckitt & Colman Inc | Control of dust particles |
| TW384207B (en) | 1997-08-20 | 2000-03-11 | Fumakilla Ltd | Piezoelectric chemical-liquid atomizer apparatus and method for repelling or eliminating harmful organism |
| US6548085B1 (en) | 1998-04-15 | 2003-04-15 | Woodstream Corporation | Insecticidal compositions and method of controlling insect pests using same |
| US6646011B2 (en) | 1998-06-03 | 2003-11-11 | Johnson & Johnson Consumer Companies, Inc. | Insect repellant compositions |
| JP4776757B2 (en) | 1999-10-01 | 2011-09-21 | 株式会社ダイゾー | Aerosol composition |
| AR029677A1 (en) | 2000-06-29 | 2003-07-10 | Bayer Ag | COMBINATIONS OF ACTIVE COMPOUNDS WITH INSECTICIDES AND ACARICIDES |
| US6719959B1 (en) | 2000-11-28 | 2004-04-13 | Avon Products, Inc. | Extended duration insect repellent composition and method of application to the skin |
| US6969521B1 (en) | 2000-11-28 | 2005-11-29 | Avon Products, Inc. | Aerosol insect repellent composition having low VOC content and method of applying same to the skin |
| EP1269842B1 (en) | 2001-06-20 | 2004-10-20 | Flit S.A. | Method for controlling the application of an insecticide and composition therefor |
| MXPA06001532A (en) | 2003-08-08 | 2006-05-15 | Fumakilla Ltd | Aerosol for controlling insect pests. |
| US7341736B2 (en) | 2004-01-30 | 2008-03-11 | S.C. Johnson & Son, Inc. | Aerosol spray resistant to discoloration |
| EP1617606A1 (en) * | 2004-07-16 | 2006-01-18 | Matsushita Electric Industrial Co., Ltd. | Scheduling mode switching for uplink transmissions |
| JP2008534684A (en) | 2005-04-04 | 2008-08-28 | バレント バイオサイエンシス コーポレーション | Stable pesticide concentrates and end-use emulsions |
| GB0508152D0 (en) * | 2005-04-22 | 2005-06-01 | Reckitt Benckiser Au Pty Ltd | Aerosol insecticide composition |
| GB0615473D0 (en) | 2006-08-03 | 2006-09-13 | Livie Biopesticides Ltd | Insecticidal composition |
| GB0615475D0 (en) * | 2006-08-03 | 2006-09-13 | Livie Biopesticides Ltd | Insecticidal composition-dill oil |
| AR063704A1 (en) | 2006-09-14 | 2009-02-11 | Makhteshim Chem Works Ltd | PESTICIDE NANOPARTICLES OBTAINED OBTAINED FROM MICROEMULSIONS AND NANOEMULSIONS |
| ITRE20060144A1 (en) | 2006-11-23 | 2008-05-24 | Re Le Vi Spa | ACARICIDAL COMPOSITION |
| JP5326318B2 (en) | 2007-03-30 | 2013-10-30 | 住友化学株式会社 | Pest control aerosol composition |
| BE1018002A5 (en) | 2008-02-18 | 2010-03-02 | Chimac | CONCENTRATED COMPOSITION OF PYRETHRINOID OR PYRETHRE. |
| GB0900874D0 (en) * | 2009-01-20 | 2009-03-04 | Reckitt & Colman Overseas | Insecticidal composition |
| WO2010086872A1 (en) | 2009-01-29 | 2010-08-05 | Director General, Defence Research & Development Organisation | A wool care composition |
| US8603640B2 (en) | 2009-03-13 | 2013-12-10 | Michael Kennedy | Hydrofluoroalkanes as carrier solvents for timber preservation |
| EP2424370A2 (en) | 2009-04-28 | 2012-03-07 | BASF Corporation | Foamable pesticide compositions |
| AR076484A1 (en) | 2009-04-28 | 2011-06-15 | Basf Corp | COMPOSITIONS AND APPLICATORS OF PESTICIDES |
| EA201200375A1 (en) | 2009-08-28 | 2012-09-28 | Басф Корпорейшн | RECESSABLE PESTICIDAL COMPOSITIONS AND APPLICATION METHODS |
| CN102548416B (en) | 2009-09-29 | 2013-11-13 | 巴斯夫欧洲公司 | Pesticidal mixtures |
| WO2011155630A1 (en) | 2010-06-11 | 2011-12-15 | 株式会社ダイゾー | Aerosol composition |
| US8475769B2 (en) | 2010-06-25 | 2013-07-02 | S.C. Johnson & Son, Inc. | Aerosol composition with enhanced dispersion effects |
| CA2840831C (en) | 2011-07-08 | 2017-11-07 | S. C. Johnson & Son, Inc. | Compressed gas aerosols with enhanced intensity and longevity of actives |
| MX356989B (en) | 2011-07-13 | 2018-06-22 | Clarke Mosquito Control Products Inc | Insecticidal compositions and methods of using the same. |
| WO2013041975A2 (en) | 2011-08-23 | 2013-03-28 | Vive Crop Protection Inc. | Pyrethroid formulations |
| WO2015133318A1 (en) | 2014-03-04 | 2015-09-11 | 大日本除蟲菊株式会社 | Aerosol for mosquito control and mosquito control method |
-
2017
- 2017-05-22 US US15/601,393 patent/US10405552B2/en active Active
-
2018
- 2018-05-18 MX MX2019014032A patent/MX2019014032A/en unknown
- 2018-05-18 WO PCT/US2018/033322 patent/WO2018217554A1/en not_active Ceased
- 2018-05-22 AR ARP180101354A patent/AR111821A1/en active IP Right Grant
-
2019
- 2019-07-31 US US16/527,595 patent/US10945436B2/en active Active
- 2019-11-20 PH PH12019502604A patent/PH12019502604A1/en unknown
Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5091183A (en) * | 1989-09-14 | 1992-02-25 | Sumitomo Chemical Company, Limited | Insecticidal and/or acaricidal composition |
| WO2014040720A1 (en) * | 2012-09-14 | 2014-03-20 | Aragon Net Ltd. | Insecticidal aerosol |
| WO2015159772A1 (en) * | 2014-04-18 | 2015-10-22 | 大日本除蟲菊株式会社 | Mosquito control aerosol and mosquito control method |
| CN104522040A (en) * | 2014-12-24 | 2015-04-22 | 东莞市绿雅达有害生物防制技术有限公司 | Invertebrate pest control agent mixture and preparation method thereof |
Non-Patent Citations (2)
| Title |
|---|
| CHEMWATCH: "REGISTERED PESTICIDES LIST - PART I", CHEMWATCH.NET, 20 April 2016 (2016-04-20), pages 1 - 7, XP055491433, Retrieved from the Internet <URL:http://full.chemwatch.net/galleria/LEGSREGS/30-2-4-8-852-3-AA-20160420.pdf> [retrieved on 20180710] * |
| YAN H ET AL: "Simultaneous determination of nine pyrethroids in indoor insecticide products by capillary gas chromatography", JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS, NEW YORK, NY, US, vol. 51, no. 3, 5 February 2010 (2010-02-05), pages 774 - 777, XP026740751, ISSN: 0731-7085, [retrieved on 20091007], DOI: 10.1016/J.JPBA.2009.09.048 * |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2025016887A1 (en) | 2023-07-14 | 2025-01-23 | Reckitt & Colman (Overseas) Hygiene Home Limited | Pest control composition |
| WO2026046842A1 (en) | 2024-08-26 | 2026-03-05 | Reckitt & Colman (Overseas) Hygiene Home Limited | Pest control composition |
Also Published As
| Publication number | Publication date |
|---|---|
| PH12019502604A1 (en) | 2020-09-28 |
| MX2019014032A (en) | 2020-02-17 |
| US20180332854A1 (en) | 2018-11-22 |
| BR112019024465A2 (en) | 2020-06-16 |
| US10945436B2 (en) | 2021-03-16 |
| US20190350205A1 (en) | 2019-11-21 |
| AR111821A1 (en) | 2019-08-21 |
| US10405552B2 (en) | 2019-09-10 |
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