USH692H - Pest control - Google Patents
Pest control Download PDFInfo
- Publication number
- USH692H USH692H US07/151,237 US15123787A USH692H US H692 H USH692 H US H692H US 15123787 A US15123787 A US 15123787A US H692 H USH692 H US H692H
- Authority
- US
- United States
- Prior art keywords
- compound
- formula
- animal
- animals
- decamethrin
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Abandoned
Links
- 241000607479 Yersinia pestis Species 0.000 title description 3
- 241001465754 Metazoa Species 0.000 claims abstract description 30
- 238000000034 method Methods 0.000 claims abstract description 4
- YMGUBTXCNDTFJI-UHFFFAOYSA-N cyclopropanecarboxylic acid Chemical compound OC(=O)C1CC1 YMGUBTXCNDTFJI-UHFFFAOYSA-N 0.000 claims description 2
- 231100000252 nontoxic Toxicity 0.000 claims description 2
- 230000003000 nontoxic effect Effects 0.000 claims description 2
- 238000000151 deposition Methods 0.000 claims 1
- 230000001846 repelling effect Effects 0.000 claims 1
- 150000001875 compounds Chemical class 0.000 abstract description 32
- 241000255925 Diptera Species 0.000 abstract description 17
- 206010061217 Infestation Diseases 0.000 abstract description 6
- 241000238631 Hexapoda Species 0.000 abstract description 5
- 230000002265 prevention Effects 0.000 abstract description 3
- 101100386054 Saccharomyces cerevisiae (strain ATCC 204508 / S288c) CYS3 gene Proteins 0.000 abstract 1
- 101150035983 str1 gene Proteins 0.000 abstract 1
- 239000000203 mixture Substances 0.000 description 26
- 238000009472 formulation Methods 0.000 description 20
- 229960002483 decamethrin Drugs 0.000 description 12
- OWZREIFADZCYQD-NSHGMRRFSA-N deltamethrin Chemical compound CC1(C)[C@@H](C=C(Br)Br)[C@H]1C(=O)O[C@H](C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 OWZREIFADZCYQD-NSHGMRRFSA-N 0.000 description 12
- 239000007921 spray Substances 0.000 description 10
- 230000000694 effects Effects 0.000 description 8
- 241001494479 Pecora Species 0.000 description 7
- 241001494115 Stomoxys calcitrans Species 0.000 description 7
- 239000003921 oil Substances 0.000 description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
- 239000000443 aerosol Substances 0.000 description 6
- 239000002904 solvent Substances 0.000 description 6
- -1 2-benzyl-4-furylmethyl Chemical group 0.000 description 5
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 5
- VXSIXFKKSNGRRO-MXOVTSAMSA-N [(1s)-2-methyl-4-oxo-3-[(2z)-penta-2,4-dienyl]cyclopent-2-en-1-yl] (1r,3r)-2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropane-1-carboxylate;[(1s)-2-methyl-4-oxo-3-[(2z)-penta-2,4-dienyl]cyclopent-2-en-1-yl] (1r,3r)-3-[(e)-3-methoxy-2-methyl-3-oxoprop-1-enyl Chemical class CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)O[C@@H]1C(C)=C(C\C=C/C=C)C(=O)C1.CC1(C)[C@H](/C=C(\C)C(=O)OC)[C@H]1C(=O)O[C@@H]1C(C)=C(C\C=C/C=C)C(=O)C1 VXSIXFKKSNGRRO-MXOVTSAMSA-N 0.000 description 5
- 239000002728 pyrethroid Substances 0.000 description 5
- 239000000243 solution Substances 0.000 description 5
- 239000000725 suspension Substances 0.000 description 5
- 241000699670 Mus sp. Species 0.000 description 4
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 4
- 239000007900 aqueous suspension Substances 0.000 description 4
- 239000005667 attractant Substances 0.000 description 4
- 239000012895 dilution Substances 0.000 description 4
- 238000010790 dilution Methods 0.000 description 4
- 235000013601 eggs Nutrition 0.000 description 4
- 230000000749 insecticidal effect Effects 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- HYJYGLGUBUDSLJ-UHFFFAOYSA-N pyrethrin Natural products CCC(=O)OC1CC(=C)C2CC3OC3(C)C2C2OC(=O)C(=C)C12 HYJYGLGUBUDSLJ-UHFFFAOYSA-N 0.000 description 4
- 229940070846 pyrethrins Drugs 0.000 description 4
- 239000002453 shampoo Substances 0.000 description 4
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- 241000257232 Haematobia irritans Species 0.000 description 3
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 3
- 241000736227 Lucilia sericata Species 0.000 description 3
- 230000031902 chemoattractant activity Effects 0.000 description 3
- 239000004495 emulsifiable concentrate Substances 0.000 description 3
- 239000003995 emulsifying agent Substances 0.000 description 3
- 150000002148 esters Chemical class 0.000 description 3
- 239000003960 organic solvent Substances 0.000 description 3
- 239000004540 pour-on Substances 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- ISWHYOCZSAWJRF-UHFFFAOYSA-N 1-[cyano-(3-phenoxyphenyl)methyl]-3-(2,2-dibromoethenyl)-2,2-dimethylcyclopropane-1-carboxylic acid Chemical compound CC1(C)C(C=C(Br)Br)C1(C(O)=O)C(C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 ISWHYOCZSAWJRF-UHFFFAOYSA-N 0.000 description 2
- 241000238876 Acari Species 0.000 description 2
- 239000005995 Aluminium silicate Substances 0.000 description 2
- 241000283690 Bos taurus Species 0.000 description 2
- LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 description 2
- 241000257159 Musca domestica Species 0.000 description 2
- 241000257226 Muscidae Species 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 239000004480 active ingredient Substances 0.000 description 2
- 235000012211 aluminium silicate Nutrition 0.000 description 2
- 239000001273 butane Substances 0.000 description 2
- 239000000969 carrier Substances 0.000 description 2
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
- 239000003085 diluting agent Substances 0.000 description 2
- 238000007598 dipping method Methods 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 235000011187 glycerol Nutrition 0.000 description 2
- 239000002917 insecticide Substances 0.000 description 2
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 2
- 230000003287 optical effect Effects 0.000 description 2
- RLLPVAHGXHCWKJ-UHFFFAOYSA-N permethrin Chemical compound CC1(C)C(C=C(Cl)Cl)C1C(=O)OCC1=CC=CC(OC=2C=CC=CC=2)=C1 RLLPVAHGXHCWKJ-UHFFFAOYSA-N 0.000 description 2
- 229960000490 permethrin Drugs 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 239000001294 propane Substances 0.000 description 2
- 230000001681 protective effect Effects 0.000 description 2
- 239000004094 surface-active agent Substances 0.000 description 2
- 239000000454 talc Substances 0.000 description 2
- 229910052623 talc Inorganic materials 0.000 description 2
- 230000003442 weekly effect Effects 0.000 description 2
- 239000000080 wetting agent Substances 0.000 description 2
- IAKOZHOLGAGEJT-UHFFFAOYSA-N 1,1,1-trichloro-2,2-bis(p-methoxyphenyl)-Ethane Chemical compound C1=CC(OC)=CC=C1C(C(Cl)(Cl)Cl)C1=CC=C(OC)C=C1 IAKOZHOLGAGEJT-UHFFFAOYSA-N 0.000 description 1
- ZMZNPVSNGBQGRW-UHFFFAOYSA-N 3-(2,2-dichloroethenyl)-2,2-dimethyl-1-[(3-phenoxyphenyl)methyl]cyclopropane-1-carboxylic acid Chemical compound CC1(C)C(C=C(Cl)Cl)C1(C(O)=O)CC1=CC=CC(OC=2C=CC=CC=2)=C1 ZMZNPVSNGBQGRW-UHFFFAOYSA-N 0.000 description 1
- 241000238421 Arthropoda Species 0.000 description 1
- 241000257160 Calliphora Species 0.000 description 1
- 241000282472 Canis lupus familiaris Species 0.000 description 1
- 208000035473 Communicable disease Diseases 0.000 description 1
- LVZWSLJZHVFIQJ-UHFFFAOYSA-N Cyclopropane Chemical group C1CC1 LVZWSLJZHVFIQJ-UHFFFAOYSA-N 0.000 description 1
- YVGGHNCTFXOJCH-UHFFFAOYSA-N DDT Chemical compound C1=CC(Cl)=CC=C1C(C(Cl)(Cl)Cl)C1=CC=C(Cl)C=C1 YVGGHNCTFXOJCH-UHFFFAOYSA-N 0.000 description 1
- 241000202828 Dermatobia hominis Species 0.000 description 1
- 239000004338 Dichlorodifluoromethane Substances 0.000 description 1
- 241000283086 Equidae Species 0.000 description 1
- 241000287828 Gallus gallus Species 0.000 description 1
- 241000257324 Glossina <genus> Species 0.000 description 1
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 1
- 241001608644 Hippoboscidae Species 0.000 description 1
- 241000238729 Hydrotaea Species 0.000 description 1
- 241000543830 Hypoderma bovis Species 0.000 description 1
- 241000257174 Hypoderma lineatum Species 0.000 description 1
- 241000257162 Lucilia <blowfly> Species 0.000 description 1
- 229920000715 Mucilage Polymers 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 241000257191 Oestridae Species 0.000 description 1
- 241000543819 Oestrus ovis Species 0.000 description 1
- 241001674048 Phthiraptera Species 0.000 description 1
- 229920003171 Poly (ethylene oxide) Chemical class 0.000 description 1
- 241000134399 Simulium sp. Species 0.000 description 1
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- 241000255628 Tabanidae Species 0.000 description 1
- 241000255626 Tabanus <genus> Species 0.000 description 1
- 206010052428 Wound Diseases 0.000 description 1
- 208000027418 Wounds and injury Diseases 0.000 description 1
- 210000001015 abdomen Anatomy 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 125000003158 alcohol group Chemical group 0.000 description 1
- 150000001335 aliphatic alkanes Chemical class 0.000 description 1
- 239000012874 anionic emulsifier Substances 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 description 1
- 239000003139 biocide Substances 0.000 description 1
- VEMKTZHHVJILDY-UXHICEINSA-N bioresmethrin Chemical compound CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)OCC1=COC(CC=2C=CC=CC=2)=C1 VEMKTZHHVJILDY-UXHICEINSA-N 0.000 description 1
- 229950002373 bioresmethrin Drugs 0.000 description 1
- 239000008280 blood Substances 0.000 description 1
- 210000004369 blood Anatomy 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 235000013330 chicken meat Nutrition 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 239000006184 cosolvent Substances 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- FHIVAFMUCKRCQO-UHFFFAOYSA-N diazinon Chemical compound CCOP(=S)(OCC)OC1=CC(C)=NC(C(C)C)=N1 FHIVAFMUCKRCQO-UHFFFAOYSA-N 0.000 description 1
- PXBRQCKWGAHEHS-UHFFFAOYSA-N dichlorodifluoromethane Chemical compound FC(F)(Cl)Cl PXBRQCKWGAHEHS-UHFFFAOYSA-N 0.000 description 1
- 229940042935 dichlorodifluoromethane Drugs 0.000 description 1
- 235000019404 dichlorodifluoromethane Nutrition 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 238000010410 dusting Methods 0.000 description 1
- 244000078703 ectoparasite Species 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 239000000499 gel Substances 0.000 description 1
- 238000003197 gene knockdown Methods 0.000 description 1
- 239000008103 glucose Substances 0.000 description 1
- 239000004519 grease Substances 0.000 description 1
- 238000000265 homogenisation Methods 0.000 description 1
- 208000015181 infectious disease Diseases 0.000 description 1
- 230000007794 irritation Effects 0.000 description 1
- 229960004592 isopropanol Drugs 0.000 description 1
- 239000003350 kerosene Substances 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 230000000670 limiting effect Effects 0.000 description 1
- 229940057995 liquid paraffin Drugs 0.000 description 1
- 244000144972 livestock Species 0.000 description 1
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Natural products C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 1
- 239000010445 mica Substances 0.000 description 1
- 229910052618 mica group Inorganic materials 0.000 description 1
- 235000013336 milk Nutrition 0.000 description 1
- 239000008267 milk Substances 0.000 description 1
- 210000004080 milk Anatomy 0.000 description 1
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
- 239000012875 nonionic emulsifier Substances 0.000 description 1
- 239000002674 ointment Substances 0.000 description 1
- 239000003883 ointment base Substances 0.000 description 1
- 230000017448 oviposition Effects 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 244000045947 parasite Species 0.000 description 1
- 239000006072 paste Substances 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 238000002203 pretreatment Methods 0.000 description 1
- 239000003380 propellant Substances 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- 238000010561 standard procedure Methods 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000000375 suspending agent Substances 0.000 description 1
- 230000008719 thickening Effects 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 230000000699 topical effect Effects 0.000 description 1
- 230000004580 weight loss Effects 0.000 description 1
- 239000004563 wettable powder Substances 0.000 description 1
- 210000002268 wool Anatomy 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/275—Nitriles; Isonitriles
Definitions
- This invention concerns the new use of known compounds and formulations containing them.
- Flies of the Order Diptera are a source of concern in animal husbandry as troublesome pests of many domestic animals. Apart from infesting animal wounds with eggs which mature in the flesh, they transmit a variety of infectious diseases by biting the animals, and can cause weight loss and decrease in milk yield.
- a variety of insecticides have been shown to be active against such flies, and some have found commercial application in preventing or limiting irritation of the animals. Such preparations have included DDT, pyrethrins, methoxychlor and diazinon, but all known remedies have at least one of the drawbacks of little or no repellant action on the flies, low insecticidal activity, and poor residual effects.
- a repellant effect of an insecticide is of particular importance in minimising fly worry or preventing the fly from attaching itself to the host thus decreasing the annoyance to the animal and the risk of infection.
- Pyrethrins in particular are recognized to have little commercial potential as repellants for nuisance flies and have further found little commercial application in the control of other arthropod ectoparasites of animals such as ticks, lice, mites and keds.
- the synthetic pyrethroid analogues of pyrethrins the compound bioresmethrin (2-benzyl-4-furylmethyl d-trans chrysanthemate) is known to be outstanding as a killing agent as measured by for example results obtained from topical application of the compound to adult houseflies (Musca domestica) but has been found to have only limited knock-down activity against these flies compared with that of pyrethrins.
- the compound permethrin, 3-phenoxybenzyl-2,2-dimethyl-3-(2,2-dichlorovinyl)cyclopropane-1-carboxylate is known from Belgian Patent No. 818820 to provide a protective effect for livestock against attack by insects of the Order Diptera and that this effect includes a repellant effect, an insecticidal effect and a residual effect.
- the structural formula (I) is intended to cover all the geometric and optical isomers of the compound including the (+)-cis-isomer, the (+)-trans-isomer, the ( ⁇ )-trans-isomer, the ( ⁇ )-cis-isomer and the ( ⁇ )-cis-trans-isomer (the sterochemistry referring to that of the cyclopropane rings).
- the alcohol moiety of the ester of formula (I) may be selected from the (-)-isomer, the (+)-isomer and the ( ⁇ )-isomer.
- the preferred isomer is (-)- ⁇ -cyano-3-phenoxybenxyl-(+)-cis-2,2-dimethyl-3-(2,2-dibromovinyl)cyclopropane-1-carboxylate.
- the compounds of formula (I) provide animals with a remarkable protective effect against attack by insects of the Order Diptera, and that this effect includes a high repellant effect, an excellent insecticidal effect, and long residual protection of the animals against infestation when the compounds of formula (I) are used at substantially lower doses than have hitherto been used for permethrin and for pyrethrins.
- the compounds are very effective in protecting cattle against the stable fly (Stomoxys calcitrans) the horn fly (Haematobia irritans) and the buffalo fly (Lyperosia exigua).
- the compounds of formula (I) may be used in the protection of a variety of animals against Diptera, which include cattle, horses, sheep and other ungulates, chickens and dogs.
- Pests which may be controlled by the use of compounds of formula (I) include Simulidae (e.g. Simulium sp.), Tabanidae (e.g. Tabanus sp.), Muscidae (e.g. Stomoxys calcitrans, Glossina sp., Lyperosia sp., Haemathobia sp., and Hydrotaea sp.), Caliphoridae (e.g. Lucilia sp., Chrysomyia sp., Calliphora sp. and Callitroga sp.) and Oestridae (e.g. Hypoderma bovis, H. lineatum, Oestrus Ovis and Dermatobia hominis).
- Simulidae e.g. Simulium sp.
- Tabanidae e.g. Tabanus sp.
- Muscidae e.g. Stomoxys calc
- the compounds of formula (I) may be used for such purposes by application of the compounds themselves or in a diluted form in known fashion as a dip, spray, foam, dust, aqueous suspension, paste, gel, shampoo, grease, aerosol, impregnated article or pour-on formulation. Dip concentrations are not applied per se, but are diluted with water and the animals immersed in a dipping bath containing the dip wash. Sprays may be applied by hand or by means of a spray race or arch. The animal may be saturated with the spray by means of high volume application or superficially coated with the spray by means of light or ultra low volume application. Aqueous suspensions may be applied to the animal in the same manner as sprays.
- Dusts may be distributed over the animals by means of a powder applicator or incorporated in perforated bags attached to trees or rubbing bars.
- Pastes, shampoos and greases may be applied manually or distributed over the surface of an inert material against which animals rub and transfer the material to their skins.
- Pour-on formulations are dispensed as a unit of liquid of relatively low volume on to the backs of animals such that all or most of the liquid is retained on the animals.
- the compounds of formula (I) may be formulated either as formulations ready for use on the animals or as formulations requiring further dilution prior to application, but both types of formulations comprise a compound of formula (I) in intimate admixture with one or more carriers or diluents.
- the carriers may be liquid, solid or gaseous or comprise mixtures of such substances, and the compound of formula (I) may be present in a concentration of from 0.025 to 99% w/v depending upon whether the formulation requires further dilution.
- Dusts may be prepared by intimate admixture of the chosen compound with a powered solid inert carrier for example suitable clays, kaolin, talc, mica, starch and diatomaceous earths.
- a powered solid inert carrier for example suitable clays, kaolin, talc, mica, starch and diatomaceous earths.
- Sprays of a compound of formula (I) may comprise a solution in an organic solvent (e.g. those listed below) or an emulsion in water (dip wash or spray wash) prepared in the field from an emulsifiable concentrate (otherwise known as a water miscible oil) which may also be used for dipping purposes.
- the concentrate preferably comprises a mixture of the active ingredient, with or without an organic solvent and one or more emulsifiers.
- Solvents may be present in wide limits but preferably in an amount of from 20 to 60% w/v of the composition and may be selected from kerosene, ketones, alkanols, xylene, aromatic naphtha, and other solvents known in the formulating art.
- concentration of emulsifiers may be varied within wide limits but preferably in the range of 5 to 25% w/v and are conveniently non-ionic surface active agents including polyoxyalkylene esters of alkyl phenols and polyoxyethylene derivatives of hexitol anhydrides.
- Dip washes may be prepared not only from emulsifiable concentrates but also from wettable powders comprising a compound of formula (I) in intimate admixture with a dispersing agent and one or more surface active agents.
- Aqueous suspensions of a compound of formula (I) may comprise a suspension in water together with suspending, stabilizing or other agents.
- the suspensions may be applied per se or in a diluted form in known fashion.
- Greases may be prepared from vegatable oils, synthetic esters of fatty acids or wool fat together with an inert base such as soft paraffin.
- a compound of formula (I) is preferably distributed uniformly through the mixture in solution or suspension.
- Greases may also be made from emulsifiable concentrates by diluting them with an ointment base.
- Pastes and shampoos are also semi-solid preparations in which a compound of formula (I) may be present as an uniform dispersion in a suitable base such as soft or liquid paraffin or made on a non-greasy basis with glycerin, mucilage or a suitable soap.
- a suitable base such as soft or liquid paraffin or made on a non-greasy basis with glycerin, mucilage or a suitable soap.
- shampoos and pastes are usually applied without further dilution they should contain the appropriate percentage of the compound of formula (I) required for treatment.
- Aerosol sprays may be prepared as a simple solution of the active ingredient in the aerosol propellant and a co-solvent such as halogenated alkanes and the solvents referred to above, respectively.
- Pour-on formulations may be made as a solution or suspension of a compound of formula (I) in a liquid medium which also contains a viscous oil to minimize spreading of the formulation on the surface of the animals.
- An animal host may be protected against infestation of Dipteran parasites by means of carrying a suitable-moulded, shaped plastic article impregnated with a compound of formula (I).
- Such articles include impregnated collars, tags, bands, sheets and strips suitably attached to appropriate parts of the body.
- the concentration of the compound of formula (I) to be applied to an animal will vary according to the isomer chosen, the nature of the formulation and the likely infestation, but in general 0.001% to 1% w/v of the compound should be present in the applied formulation.
- concentration of the compound of formula (I) to be applied to an animal will vary according to the isomer chosen, the nature of the formulation and the likely infestation, but in general 0.001% to 1% w/v of the compound should be present in the applied formulation.
- a regular application for example weekly, by standard techniques of a solution or emulsion of 0.001 to 0.1% w/v has been found to provide satisfactory control.
- the amount of the compound deposited on an animal will vary according to the method of application, the size of the animal, the concentration of the compound in the applied formulation and the nature of the formulation.
- Dusts, greases, pastes and aerosol formulations are usually applied at concentrations of 0.001 to 1.0% w/v of a compound of formula (I) in the applied formulation.
- a method of treating an animal for the prevention or control of infestation of insects of the Order Diptera which comprises application to the animal of a non-toxic infestation prevention or control effective amount of ⁇ -cyano-3-phenoxybenzyl-2,2-dimethyl-3-(2,2-dibromovinyl)cyclopropane-1-carboxylate or of a formulation comprising said compound in intimate admixture with a carrier or diluent therefor.
- Decamethrin refers to (-)- ⁇ -cyano-3-phenoxybenzyl-(+)-cis-2,2-dimethyl-3-(2,2-dibromovinyl) cyclopropane-1-carboxylate.
- mice were sprayed with a range of washes, at differing concentrations of Decamethrin (each wash comprising Decamethrin dissolved in an organic solvent and emulsifiers and emulsified in water), and the mice allowed to clean themselves and dry. After a period of 4 hours the mice were anaesthetised and strapped over gauze boxes containing adult Stomoxys calcitrans previously starved for 24 hours, and the host and flies allowed to remain in contact. After 0.5 hour and flies were anaesthetised, squashed between filter paper and the number having blood in the abdomen counted.
- Decamethrin each wash comprising Decamethrin dissolved in an organic solvent and emulsifiers and emulsified in water
- the % of repelled flies against the concentration of Decamethrin applied to the mice is plotted and the RC 50 and RC 99 values (the concentration of Decamethrin which repels 50% and 99% of the flies respectively) is calculated from the regression line.
- Friesian steers matched for their susceptibility to S. calcitrans were arranged into groups according to susceptibility. Each steer in a group was sprayed at 7 or 14 day intervals with 1 liter of wash containing Decamethrin at a certain concentration; steers of other groups were sprayed with washes of other concentrations. (The washes were prepared by appropriate dilution of a 20% w/v miscible-oil and applied to the animal as a light tip-spray by means of a knapsack sprayer).
- Exposures of starved adult S. calcitrans were made before and after treatment and the number of flies alighting on each steer during the exposure was counted.
- the length of protection afforded was determined by the selection of a value of 67% of the pre-treatment count of S. calcitrans as the break-point.
- control and test sheep were then exposed to gravid, female, Lucilia sericata (N strain). Six hours later a comparison was made between the number of eggs laid on the dipped as opposed to the undipped sheep by estimating the number of eggs present in each cluster.
- Celite 209 is an inert carrier.
- Perminal BX and Dispersol AC are wetting agents.
- Esso 200 Solvent is a mobile oil which consists of 95% of aromatic hydrocarbons.
- the butane/propane mixture is chosen so as to have a pressure of 40 pounds per square inch at 21° C.
- Aerosol OTB is a wetting agent.
- Keltrol is a thickening/suspending agent.
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
A method of treating an animal for the prevention or control of infestation by insects of the Order Diptera which comprises application to the animal of a compound of formula ##STR1##
Description
This is a continuation of co-pending application Ser. No. 365,532, filed on Apr. 5, 1982, which is a divisional of Ser. No. 213,930, filed on Dec. 8, 1980, now abandoned, which is a continuation of Ser. No. 29,337, filed on Apr. 12, 1979, now abandoned, which is a continuation of Ser. No. 863,736, filed on Dec. 23, 1977, now abandoned.
This invention concerns the new use of known compounds and formulations containing them.
Flies of the Order Diptera are a source of concern in animal husbandry as troublesome pests of many domestic animals. Apart from infesting animal wounds with eggs which mature in the flesh, they transmit a variety of infectious diseases by biting the animals, and can cause weight loss and decrease in milk yield.
A variety of insecticides have been shown to be active against such flies, and some have found commercial application in preventing or limiting irritation of the animals. Such preparations have included DDT, pyrethrins, methoxychlor and diazinon, but all known remedies have at least one of the drawbacks of little or no repellant action on the flies, low insecticidal activity, and poor residual effects. A repellant effect of an insecticide is of particular importance in minimising fly worry or preventing the fly from attaching itself to the host thus decreasing the annoyance to the animal and the risk of infection.
Pyrethrins in particular are recognized to have little commercial potential as repellants for nuisance flies and have further found little commercial application in the control of other arthropod ectoparasites of animals such as ticks, lice, mites and keds. Amongst the synthetic pyrethroid analogues of pyrethrins the compound bioresmethrin (2-benzyl-4-furylmethyl d-trans chrysanthemate) is known to be outstanding as a killing agent as measured by for example results obtained from topical application of the compound to adult houseflies (Musca domestica) but has been found to have only limited knock-down activity against these flies compared with that of pyrethrins.
The compound permethrin, 3-phenoxybenzyl-2,2-dimethyl-3-(2,2-dichlorovinyl)cyclopropane-1-carboxylate is known from Belgian Patent No. 818820 to provide a protective effect for livestock against attack by insects of the Order Diptera and that this effect includes a repellant effect, an insecticidal effect and a residual effect.
α-Cyano-3-phenoxybenzyl-2,2-dimethyl-3-(2,2-dibromovinyl)cyclopropane-1-carboxylate, and its optical and geometrical isomers, (hereinafter referred to as the compounds of formula (I) are known (from U.K. Patent Nos. 1,413,491 and 1,448,228) to have insecticidal activity against a variety of insects including Musca domestica. ##STR2##
The structural formula (I) is intended to cover all the geometric and optical isomers of the compound including the (+)-cis-isomer, the (+)-trans-isomer, the (±)-trans-isomer, the (±)-cis-isomer and the (±)-cis-trans-isomer (the sterochemistry referring to that of the cyclopropane rings). Moreover the alcohol moiety of the ester of formula (I) may be selected from the (-)-isomer, the (+)-isomer and the (±)-isomer. The preferred isomer is (-)-α-cyano-3-phenoxybenxyl-(+)-cis-2,2-dimethyl-3-(2,2-dibromovinyl)cyclopropane-1-carboxylate.
It has now been found that the compounds of formula (I) provide animals with a remarkable protective effect against attack by insects of the Order Diptera, and that this effect includes a high repellant effect, an excellent insecticidal effect, and long residual protection of the animals against infestation when the compounds of formula (I) are used at substantially lower doses than have hitherto been used for permethrin and for pyrethrins. In particular the compounds are very effective in protecting cattle against the stable fly (Stomoxys calcitrans) the horn fly (Haematobia irritans) and the buffalo fly (Lyperosia exigua).
The compounds of formula (I) may be used in the protection of a variety of animals against Diptera, which include cattle, horses, sheep and other ungulates, chickens and dogs.
Pests which may be controlled by the use of compounds of formula (I) include Simulidae (e.g. Simulium sp.), Tabanidae (e.g. Tabanus sp.), Muscidae (e.g. Stomoxys calcitrans, Glossina sp., Lyperosia sp., Haemathobia sp., and Hydrotaea sp.), Caliphoridae (e.g. Lucilia sp., Chrysomyia sp., Calliphora sp. and Callitroga sp.) and Oestridae (e.g. Hypoderma bovis, H. lineatum, Oestrus Ovis and Dermatobia hominis).
The compounds of formula (I) may be used for such purposes by application of the compounds themselves or in a diluted form in known fashion as a dip, spray, foam, dust, aqueous suspension, paste, gel, shampoo, grease, aerosol, impregnated article or pour-on formulation. Dip concentrations are not applied per se, but are diluted with water and the animals immersed in a dipping bath containing the dip wash. Sprays may be applied by hand or by means of a spray race or arch. The animal may be saturated with the spray by means of high volume application or superficially coated with the spray by means of light or ultra low volume application. Aqueous suspensions may be applied to the animal in the same manner as sprays. Dusts may be distributed over the animals by means of a powder applicator or incorporated in perforated bags attached to trees or rubbing bars. Pastes, shampoos and greases may be applied manually or distributed over the surface of an inert material against which animals rub and transfer the material to their skins. Pour-on formulations are dispensed as a unit of liquid of relatively low volume on to the backs of animals such that all or most of the liquid is retained on the animals.
The compounds of formula (I) may be formulated either as formulations ready for use on the animals or as formulations requiring further dilution prior to application, but both types of formulations comprise a compound of formula (I) in intimate admixture with one or more carriers or diluents. The carriers may be liquid, solid or gaseous or comprise mixtures of such substances, and the compound of formula (I) may be present in a concentration of from 0.025 to 99% w/v depending upon whether the formulation requires further dilution.
Dusts may be prepared by intimate admixture of the chosen compound with a powered solid inert carrier for example suitable clays, kaolin, talc, mica, starch and diatomaceous earths.
Sprays of a compound of formula (I) may comprise a solution in an organic solvent (e.g. those listed below) or an emulsion in water (dip wash or spray wash) prepared in the field from an emulsifiable concentrate (otherwise known as a water miscible oil) which may also be used for dipping purposes. The concentrate preferably comprises a mixture of the active ingredient, with or without an organic solvent and one or more emulsifiers. Solvents may be present in wide limits but preferably in an amount of from 20 to 60% w/v of the composition and may be selected from kerosene, ketones, alkanols, xylene, aromatic naphtha, and other solvents known in the formulating art. The concentration of emulsifiers may be varied within wide limits but preferably in the range of 5 to 25% w/v and are conveniently non-ionic surface active agents including polyoxyalkylene esters of alkyl phenols and polyoxyethylene derivatives of hexitol anhydrides.
Dip washes may be prepared not only from emulsifiable concentrates but also from wettable powders comprising a compound of formula (I) in intimate admixture with a dispersing agent and one or more surface active agents.
Aqueous suspensions of a compound of formula (I) may comprise a suspension in water together with suspending, stabilizing or other agents. The suspensions may be applied per se or in a diluted form in known fashion.
Greases (or ointments) may be prepared from vegatable oils, synthetic esters of fatty acids or wool fat together with an inert base such as soft paraffin.
A compound of formula (I) is preferably distributed uniformly through the mixture in solution or suspension. Greases may also be made from emulsifiable concentrates by diluting them with an ointment base.
Pastes and shampoos are also semi-solid preparations in which a compound of formula (I) may be present as an uniform dispersion in a suitable base such as soft or liquid paraffin or made on a non-greasy basis with glycerin, mucilage or a suitable soap. As greases, shampoos and pastes are usually applied without further dilution they should contain the appropriate percentage of the compound of formula (I) required for treatment.
Aerosol sprays may be prepared as a simple solution of the active ingredient in the aerosol propellant and a co-solvent such as halogenated alkanes and the solvents referred to above, respectively. Pour-on formulations may be made as a solution or suspension of a compound of formula (I) in a liquid medium which also contains a viscous oil to minimize spreading of the formulation on the surface of the animals.
An animal host may be protected against infestation of Dipteran parasites by means of carrying a suitable-moulded, shaped plastic article impregnated with a compound of formula (I). Such articles include impregnated collars, tags, bands, sheets and strips suitably attached to appropriate parts of the body.
The concentration of the compound of formula (I) to be applied to an animal will vary according to the isomer chosen, the nature of the formulation and the likely infestation, but in general 0.001% to 1% w/v of the compound should be present in the applied formulation. For the control of biting flies, a regular application, for example weekly, by standard techniques of a solution or emulsion of 0.001 to 0.1% w/v has been found to provide satisfactory control. It will be understood that the amount of the compound deposited on an animal will vary according to the method of application, the size of the animal, the concentration of the compound in the applied formulation and the nature of the formulation.
Dusts, greases, pastes and aerosol formulations are usually applied at concentrations of 0.001 to 1.0% w/v of a compound of formula (I) in the applied formulation.
It will be appreciated from the foregoing that what we will claim may comprise any novel feature described herein, principally and not exclusively, for example:
(a) A method of treating an animal for the prevention or control of infestation of insects of the Order Diptera which comprises application to the animal of a non-toxic infestation prevention or control effective amount of α-cyano-3-phenoxybenzyl-2,2-dimethyl-3-(2,2-dibromovinyl)cyclopropane-1-carboxylate or of a formulation comprising said compound in intimate admixture with a carrier or diluent therefor.
The following Examples illustrate the present invention and the manner in which it may be carried out but should not be construed as in any way constituting a limitation thereof. In the Examples, Decamethrin refers to (-)-α-cyano-3-phenoxybenzyl-(+)-cis-2,2-dimethyl-3-(2,2-dibromovinyl) cyclopropane-1-carboxylate.
Groups of mice were sprayed with a range of washes, at differing concentrations of Decamethrin (each wash comprising Decamethrin dissolved in an organic solvent and emulsifiers and emulsified in water), and the mice allowed to clean themselves and dry. After a period of 4 hours the mice were anaesthetised and strapped over gauze boxes containing adult Stomoxys calcitrans previously starved for 24 hours, and the host and flies allowed to remain in contact. After 0.5 hour and flies were anaesthetised, squashed between filter paper and the number having blood in the abdomen counted. The % of repelled flies against the concentration of Decamethrin applied to the mice is plotted and the RC50 and RC99 values (the concentration of Decamethrin which repels 50% and 99% of the flies respectively) is calculated from the regression line.
For Decamethrin the RC50 (%) was 0.0020 and the RC99 (%) was 0.02.
Friesian steers, matched for their susceptibility to S. calcitrans were arranged into groups according to susceptibility. Each steer in a group was sprayed at 7 or 14 day intervals with 1 liter of wash containing Decamethrin at a certain concentration; steers of other groups were sprayed with washes of other concentrations. (The washes were prepared by appropriate dilution of a 20% w/v miscible-oil and applied to the animal as a light tip-spray by means of a knapsack sprayer).
Exposures of starved adult S. calcitrans were made before and after treatment and the number of flies alighting on each steer during the exposure was counted.
The length of protection afforded was determined by the selection of a value of 67% of the pre-treatment count of S. calcitrans as the break-point.
The results are tabulated below:
______________________________________
Treatment Interval
Days protection
Concentration (% w/v)
days (average)
______________________________________
0.0125 7 2
0.0250 7 6
0.0500 14 9
0.0750 14 14
0.1000 14 14
______________________________________
Seven sheep were dipped in a wash containing 0.05% w/v of Decamethrin prepared from a 2.5% w/v miscible-oil. At weekly intervals post-treatment portions of the sheeps' fleece were parted and 1 to 2 drops of a fly-attractant were applied. The attractant was prepared by homogenisation of Lucilia sericata (N strain) larvae feeding on ox-liver. Glucose and saline solution were added to the homogenate to afford the attractant as a suspension. Seven control undipped sheep were similarly treated with the attractant.
The control and test sheep were then exposed to gravid, female, Lucilia sericata (N strain). Six hours later a comparison was made between the number of eggs laid on the dipped as opposed to the undipped sheep by estimating the number of eggs present in each cluster.
If a dipped sheep carried more than two eggs in any cluster protection was not regarded as being obtained.
The results obtained indicated that approximately 13 weeks protection against oviposition by adult Lucilia sericata N was afforded by the above treatment.
______________________________________
Wettable Powder Formulations
(a) % w/w
(b) % w/w
______________________________________
Decamethrin 2.5 25.0
Celite 209 68.5 51.0
Kaolin 25.0 20.0
Perminal BX 1.0 1.0
Dispersol AC 3.0 3.0
100.0 100.0
______________________________________
Celite 209 is an inert carrier.
Perminal BX and Dispersol AC are wetting agents.
______________________________________
Miscible-oil Formulations
(a) % w/w
(b) % w/w
______________________________________
Decamethrin 2.5 19.0
Cyclohexanone -- 15.0
Esso 200 Solvent 85.0 53.5
Anionic/Non-ionic Emulsifier
12.5 12.5
100.00 100.00
______________________________________
Esso 200 Solvent is a mobile oil which consists of 95% of aromatic hydrocarbons.
______________________________________
Pressure-packed Aerosol Formulations
(a) (b) (c) (d)
______________________________________
Decamcthrin 0.20 0.10 0.05 0.01
Methylene chloride
25.00 44.90 39.95
Iso-propyl alcohol
14.80 -- -- 19.99
Refined Petroleum Solvent
-- 55.00 20.00
--
50/50 Trichlorofluoro
60.00 -- -- --
methane/dichlorodifluoro
methane
Butane/Propane mixture
-- -- 40.00
Water -- -- -- 40.00
Dimethyl ether -- -- -- 40.00
100.00 100.00 100.00
100.00
______________________________________
The butane/propane mixture is chosen so as to have a pressure of 40 pounds per square inch at 21° C.
______________________________________
Dusting Powder Formulations
(a) % w/w
(b) % w/w
______________________________________
Decamethrin 0.005 1.0
Talc 99.995 99.0
100.000 100.0
______________________________________
______________________________________
Aqueous Suspensions
(a) % w/w
(b) % w/w
______________________________________
Decamethrin 5.0 20.0
Aerosol OTB 0.2 0.2
Keltrol 0.8 0.6
Water 74.0 61.2
Glycerol 20.0 15.0
100.0 100.0
______________________________________
Aerosol OTB is a wetting agent.
Keltrol is a thickening/suspending agent.
Claims (1)
1. A method of repelling flies from an animal which comprises depositing on said animal a non-toxic effective fly repellant amount of (-)-α-cyano-3-phenoxybenzyl-(+)-cis-2,2-dimethyl-3-(2,2-dibromovinyl) cyclopropane-1-carboxylate.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US07/151,237 USH692H (en) | 1977-12-23 | 1987-10-27 | Pest control |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US86373677A | 1977-12-23 | 1977-12-23 | |
| US07/151,237 USH692H (en) | 1977-12-23 | 1987-10-27 | Pest control |
Related Parent Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US06365532 Continuation | 1982-04-05 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| USH692H true USH692H (en) | 1989-10-03 |
Family
ID=26848450
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US07/151,237 Abandoned USH692H (en) | 1977-12-23 | 1987-10-27 | Pest control |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | USH692H (en) |
-
1987
- 1987-10-27 US US07/151,237 patent/USH692H/en not_active Abandoned
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US4780459A (en) | Synergistic compositions | |
| US4020181A (en) | Method of repelling insects from domestic mammals | |
| EP1372382B1 (en) | Method of repelling insects | |
| US5236954A (en) | Parasiticidal composition and methods for its making and use | |
| US4404223A (en) | Pesticidal formulations | |
| AP222A (en) | An animal pour-on pesticidal formulation. | |
| US5435992A (en) | Non-irritating pesticidal compositions | |
| GB2185685A (en) | An oil-in-water pesticidal emulsion | |
| JPS63246302A (en) | Lousicidal composition | |
| JPH0629161B2 (en) | Ectoparasiticidal preparation, its manufacturing method and ectoparasite control method | |
| EP0576594B1 (en) | Protective compositions | |
| US4897386A (en) | Synergistic compositions | |
| US5942525A (en) | Spot treatment of animals with pyriproxyfen and an insecticide | |
| GB1591105A (en) | Pest control | |
| US5290770A (en) | Synergistic compositions | |
| CA1091148A (en) | Pest control | |
| JP2790678B2 (en) | Pest repellent | |
| USH692H (en) | Pest control | |
| JPH0463841B2 (en) | ||
| EP0235979B1 (en) | Pesticidal formulations | |
| Drummond | New methods of applying drugs for the cntrol of ectoparasites | |
| Roberts | Field tests with five insecticides for the control of horn flies | |
| GB1602971A (en) | Synergistic pesticidal compositions | |
| US5096895A (en) | Novel synergistic compositions | |
| US3067091A (en) | Insect combatting |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| STCF | Information on status: patent grant |
Free format text: PATENTED CASE |