MXPA97005678A - Act insecticide composition - Google Patents
Act insecticide compositionInfo
- Publication number
- MXPA97005678A MXPA97005678A MXPA/A/1997/005678A MX9705678A MXPA97005678A MX PA97005678 A MXPA97005678 A MX PA97005678A MX 9705678 A MX9705678 A MX 9705678A MX PA97005678 A MXPA97005678 A MX PA97005678A
- Authority
- MX
- Mexico
- Prior art keywords
- composition according
- active insecticidal
- insecticidal composition
- surfactant
- active
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 94
- 239000002917 insecticide Substances 0.000 title description 3
- 230000000749 insecticidal effect Effects 0.000 claims abstract description 41
- 239000000839 emulsion Substances 0.000 claims abstract description 40
- 239000012071 phase Substances 0.000 claims abstract description 30
- 239000008346 aqueous phase Substances 0.000 claims abstract description 21
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 22
- 239000002904 solvent Substances 0.000 claims description 20
- 239000004094 surface-active agent Substances 0.000 claims description 18
- 239000003380 propellant Substances 0.000 claims description 12
- 239000004480 active ingredient Substances 0.000 claims description 11
- 239000004215 Carbon black (E152) Substances 0.000 claims description 9
- 229930195733 hydrocarbon Natural products 0.000 claims description 9
- 150000002430 hydrocarbons Chemical class 0.000 claims description 9
- 239000004615 ingredient Substances 0.000 claims description 9
- 239000002736 nonionic surfactant Substances 0.000 claims description 7
- LPXPTNMVRIOKMN-UHFFFAOYSA-M sodium nitrite Chemical group [Na+].[O-]N=O LPXPTNMVRIOKMN-UHFFFAOYSA-M 0.000 claims description 7
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims description 6
- ZORQXIQZAOLNGE-UHFFFAOYSA-N 1,1-difluorocyclohexane Chemical compound FC1(F)CCCCC1 ZORQXIQZAOLNGE-UHFFFAOYSA-N 0.000 claims description 5
- 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 claims description 5
- 239000006184 cosolvent Substances 0.000 claims description 5
- 239000001593 sorbitan monooleate Substances 0.000 claims description 5
- 229940035049 sorbitan monooleate Drugs 0.000 claims description 5
- 235000011069 sorbitan monooleate Nutrition 0.000 claims description 5
- FIPWRIJSWJWJAI-UHFFFAOYSA-N Butyl carbitol 6-propylpiperonyl ether Chemical compound C1=C(CCC)C(COCCOCCOCCCC)=CC2=C1OCO2 FIPWRIJSWJWJAI-UHFFFAOYSA-N 0.000 claims description 4
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 4
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical group C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims description 4
- 230000007797 corrosion Effects 0.000 claims description 4
- 238000005260 corrosion Methods 0.000 claims description 4
- 239000003205 fragrance Substances 0.000 claims description 4
- 229960005235 piperonyl butoxide Drugs 0.000 claims description 4
- -1 stearic Chemical group 0.000 claims description 4
- 239000003945 anionic surfactant Substances 0.000 claims description 3
- 239000003093 cationic surfactant Substances 0.000 claims description 3
- 239000003112 inhibitor Substances 0.000 claims description 3
- 229930195734 saturated hydrocarbon Natural products 0.000 claims description 3
- 235000010288 sodium nitrite Nutrition 0.000 claims description 3
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical class OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 claims description 2
- HVUMOYIDDBPOLL-XWVZOOPGSA-N Sorbitan monostearate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O HVUMOYIDDBPOLL-XWVZOOPGSA-N 0.000 claims description 2
- 125000001931 aliphatic group Chemical group 0.000 claims description 2
- 125000000129 anionic group Chemical group 0.000 claims description 2
- 125000003118 aryl group Chemical group 0.000 claims description 2
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid ester group Chemical class C(CCCCCCCCCCC)(=O)O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 claims description 2
- 150000002191 fatty alcohols Chemical class 0.000 claims description 2
- 238000005187 foaming Methods 0.000 claims description 2
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims description 2
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical group CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 claims description 2
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid group Chemical group C(CCCCCCC\C=C/CCCCCCCC)(=O)O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 claims description 2
- IPCSVZSSVZVIGE-UHFFFAOYSA-N palmitic acid group Chemical group C(CCCCCCCCCCCCCCC)(=O)O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 claims description 2
- 239000004299 sodium benzoate Substances 0.000 claims description 2
- 235000010234 sodium benzoate Nutrition 0.000 claims description 2
- 239000001587 sorbitan monostearate Substances 0.000 claims description 2
- 235000011076 sorbitan monostearate Nutrition 0.000 claims description 2
- 229940035048 sorbitan monostearate Drugs 0.000 claims description 2
- IYFATESGLOUGBX-YVNJGZBMSA-N Sorbitan monopalmitate Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O IYFATESGLOUGBX-YVNJGZBMSA-N 0.000 claims 1
- 125000003158 alcohol group Chemical group 0.000 claims 1
- WXMKPNITSTVMEF-UHFFFAOYSA-M sodium benzoate Chemical compound [Na+].[O-]C(=O)C1=CC=CC=C1 WXMKPNITSTVMEF-UHFFFAOYSA-M 0.000 claims 1
- 239000001570 sorbitan monopalmitate Substances 0.000 claims 1
- 235000011071 sorbitan monopalmitate Nutrition 0.000 claims 1
- 229940031953 sorbitan monopalmitate Drugs 0.000 claims 1
- 241000238631 Hexapoda Species 0.000 abstract description 14
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 6
- 238000003756 stirring Methods 0.000 description 5
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 4
- 239000007789 gas Substances 0.000 description 4
- 238000005507 spraying Methods 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- 229920002101 Chitin Polymers 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 239000000443 aerosol Substances 0.000 description 3
- 238000013019 agitation Methods 0.000 description 3
- 239000006185 dispersion Substances 0.000 description 3
- 239000006260 foam Substances 0.000 description 3
- 238000009472 formulation Methods 0.000 description 3
- 229960000490 permethrin Drugs 0.000 description 3
- 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 3
- HYJYGLGUBUDSLJ-UHFFFAOYSA-N pyrethrin Natural products CCC(=O)OC1CC(=C)C2CC3OC3(C)C2C2OC(=O)C(=C)C12 HYJYGLGUBUDSLJ-UHFFFAOYSA-N 0.000 description 3
- 239000002728 pyrethroid Substances 0.000 description 3
- 239000007921 spray Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- GQPLMRYTRLFLPF-UHFFFAOYSA-N Nitrous Oxide Chemical compound [O-][N+]#N GQPLMRYTRLFLPF-UHFFFAOYSA-N 0.000 description 2
- VQXSOUPNOZTNAI-UHFFFAOYSA-N Pyrethrin I Natural products CC(=CC1CC1C(=O)OC2CC(=O)C(=C2C)CC=C/C=C)C VQXSOUPNOZTNAI-UHFFFAOYSA-N 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 125000002091 cationic group Chemical group 0.000 description 2
- 235000013601 eggs Nutrition 0.000 description 2
- NNPPMTNAJDCUHE-UHFFFAOYSA-N isobutane Chemical compound CC(C)C NNPPMTNAJDCUHE-UHFFFAOYSA-N 0.000 description 2
- QWTDNUCVQCZILF-UHFFFAOYSA-N isopentane Chemical compound CCC(C)C QWTDNUCVQCZILF-UHFFFAOYSA-N 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 239000003209 petroleum derivative Substances 0.000 description 2
- 239000011148 porous material Substances 0.000 description 2
- 239000001294 propane Substances 0.000 description 2
- VJFUPGQZSXIULQ-XIGJTORUSA-N pyrethrin II Chemical compound 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 VJFUPGQZSXIULQ-XIGJTORUSA-N 0.000 description 2
- 239000005871 repellent Substances 0.000 description 2
- ZCVAOQKBXKSDMS-PVAVHDDUSA-N (+)-trans-(S)-allethrin Chemical compound CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)O[C@@H]1C(C)=C(CC=C)C(=O)C1 ZCVAOQKBXKSDMS-PVAVHDDUSA-N 0.000 description 1
- ZCVAOQKBXKSDMS-AQYZNVCMSA-N (+)-trans-allethrin Chemical compound CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)OC1C(C)=C(CC=C)C(=O)C1 ZCVAOQKBXKSDMS-AQYZNVCMSA-N 0.000 description 1
- CXBMCYHAMVGWJQ-CABCVRRESA-N (1,3-dioxo-4,5,6,7-tetrahydroisoindol-2-yl)methyl (1r,3r)-2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropane-1-carboxylate Chemical compound CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)OCN1C(=O)C(CCCC2)=C2C1=O CXBMCYHAMVGWJQ-CABCVRRESA-N 0.000 description 1
- KAATUXNTWXVJKI-NSHGMRRFSA-N (1R)-cis-(alphaS)-cypermethrin Chemical compound CC1(C)[C@@H](C=C(Cl)Cl)[C@H]1C(=O)O[C@H](C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 KAATUXNTWXVJKI-NSHGMRRFSA-N 0.000 description 1
- FJDPATXIBIBRIM-QFMSAKRMSA-N (1R)-trans-cyphenothrin Chemical compound CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)OC(C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 FJDPATXIBIBRIM-QFMSAKRMSA-N 0.000 description 1
- FMTFEIJHMMQUJI-NJAFHUGGSA-N 102130-98-3 Natural products CC=CCC1=C(C)[C@H](CC1=O)OC(=O)[C@@H]1[C@@H](C=C(C)C)C1(C)C FMTFEIJHMMQUJI-NJAFHUGGSA-N 0.000 description 1
- 239000005877 Alpha-Cypermethrin Substances 0.000 description 1
- 241000239290 Araneae Species 0.000 description 1
- 241001674044 Blattodea Species 0.000 description 1
- 239000005946 Cypermethrin Substances 0.000 description 1
- 239000005892 Deltamethrin Substances 0.000 description 1
- 241000257303 Hymenoptera Species 0.000 description 1
- 241001124553 Lepismatidae Species 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- AOMUHOFOVNGZAN-UHFFFAOYSA-N N,N-bis(2-hydroxyethyl)dodecanamide Chemical compound CCCCCCCCCCCC(=O)N(CCO)CCO AOMUHOFOVNGZAN-UHFFFAOYSA-N 0.000 description 1
- 206010052437 Nasal discomfort Diseases 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 241000238814 Orthoptera Species 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- 241000607479 Yersinia pestis Species 0.000 description 1
- 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 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
- 229940024113 allethrin Drugs 0.000 description 1
- 239000003849 aromatic solvent Substances 0.000 description 1
- 229950002373 bioresmethrin Drugs 0.000 description 1
- 239000001273 butane Substances 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 150000008280 chlorinated hydrocarbons Chemical class 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- KAATUXNTWXVJKI-UHFFFAOYSA-N cypermethrin Chemical compound CC1(C)C(C=C(Cl)Cl)C1C(=O)OC(C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 KAATUXNTWXVJKI-UHFFFAOYSA-N 0.000 description 1
- 229960005424 cypermethrin Drugs 0.000 description 1
- 229940008203 d-transallethrin Drugs 0.000 description 1
- 229960002483 decamethrin Drugs 0.000 description 1
- 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 1
- AFABGHUZZDYHJO-UHFFFAOYSA-N dimethyl butane Natural products CCCC(C)C AFABGHUZZDYHJO-UHFFFAOYSA-N 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 230000001804 emulsifying effect Effects 0.000 description 1
- 238000003912 environmental pollution Methods 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 239000001282 iso-butane Substances 0.000 description 1
- 150000002646 long chain fatty acid esters Chemical class 0.000 description 1
- 231100000053 low toxicity Toxicity 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000001272 nitrous oxide Substances 0.000 description 1
- 230000009972 noncorrosive effect Effects 0.000 description 1
- 230000000149 penetrating effect Effects 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- SBNFWQZLDJGRLK-UHFFFAOYSA-N phenothrin Chemical compound CC1(C)C(C=C(C)C)C1C(=O)OCC1=CC=CC(OC=2C=CC=CC=2)=C1 SBNFWQZLDJGRLK-UHFFFAOYSA-N 0.000 description 1
- 229960003536 phenothrin Drugs 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- 229940070846 pyrethrins Drugs 0.000 description 1
- 230000002940 repellent Effects 0.000 description 1
- 229940108410 resmethrin Drugs 0.000 description 1
- VEMKTZHHVJILDY-FIWHBWSRSA-N resmethrin Chemical compound CC1(C)[C@H](C=C(C)C)C1C(=O)OCC1=COC(CC=2C=CC=CC=2)=C1 VEMKTZHHVJILDY-FIWHBWSRSA-N 0.000 description 1
- 230000007928 solubilization Effects 0.000 description 1
- 238000005063 solubilization Methods 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 229960005199 tetramethrin Drugs 0.000 description 1
- 239000007762 w/o emulsion Substances 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Abstract
The present invention relates to: An active insecticidal composition that forms an oil-free emulsion of limited stability containing an aqueous phase and an oil phase. When this composition is sprayed on a target surface, the aqueous phase is at least partially removed from the oil phase in the air or at the time of touching the target surface. Consequently, this composition leaves no ugly milky residue. Likewise, it is highly effective to kill insect
Description
ACTIVE INSECTICIDE COMPOSITION
BACKGROUND OF THE INVENTION
FIELD OF THE INVENTION
The present invention relates to an active insecticidal composition that forms an oil-free emulsion of limited stability.
This composition when sprayed on a target surface, leaves no unpleasant milky residue. In addition, it is highly effective in killing insects.
DESCRIPTION OF THE PREVIOUS TECHNIQUE
Active insecticidal compositions are generally sprayed from a container such as an aerosol container, onto a target surface. For a successful sprinkling that is uniform and equally distributed, the composition must be homogeneous or almost homogeneous. Traditionally, many active insecticidal compositions have had a single homogenous oil phase. However, such compositions usually have a high flammability and contribute to volatile petroleum products in the atmosphere. To reduce the oil content, the compositions were developed to form a homogeneous, stable emulsion containing an aqueous phase and an oil phase, such as those described in the U.S. Patents. Nos. 3,159,535 and 3,303,091. The patent of E.U.A. No. 5,178,871 discloses a stable, double emulsion. However, when such compositions are sprayed onto a target surface, unpleasant milky residues that characterize the appearance of an emulsion often remain on the surface, at least until the composition is completely dried. Compositions have also been developed which form emulsions without water (or oil in water), wherein the aqueous phase is the continuous phase and the oil phase is the embedded or discontinuous phase, such as those described in the U.S. Patents. Nos. 4,822,613; 4,889,710 and 5,094,853. However, said compositions typically form a stable foam when sprayed on a target surface. In addition, if the active ingredient is dissolved or dispersed in the aqueous phase, the active ingredient does not effectively penetrate the surfaces of water-repellent chitin insects. The patent of E.U.A. No. 2,418,652 discloses an emulsion without water to which a cationic emulsifier has been added, although in an amount less than an emulsifying amount. The cationic material is believed to adjust the surface charge of the oil globules suspended from the emulsion without water to increase its ability to adhere to the surface of a generally negatively charged sheet. The patent of E.U.A. No. 1,707,466 discloses a concentrated, stable oil emulsion which can be diluted with water to form a stable dispersion of oil in water. Although the dispersion is described as being stable over time while in its container, it is said to be substantially broken by contact with the target surface to coat plants or insect eggs with oil, combating the scale of insects and killing the eggs of the insects. coated insects. No other insecticide other than the same oil is used. The patent of E. U.A. No. 4, 904,464 discloses an insecticidal composition containing cocodiethanolamide which is separated into different phases of water and oil, which, under agitation, form an unstable dispersion, as opposed to an oil-free emulsion, which is then separated immediately after assortment. subsequent to the agitation.
COMPENDIUM OF THE INVENTION
The inventors hereby have discovered an active, novel insecticidal composition which leaves no unpleasant milky spots when sprayed on a target surface. The composition is also highly effective in killing a variety of insects, including cockroaches, ants, silverfish, crickets and spiders. In one embodiment, the present invention provides an active insecticidal composition that forms an oil-free emulsion of limited stability, comprising: an aqueous phase comprising water; an oil phase comprising a hydrocarbon solvent and at least one active ingredient; and an amount of an effective surfactant to form an emulsion without non-foaming oil of limited stability; whereby when the emulsion is first formed inside and then sprayed from a container, the aqueous phase is at least partially separated from the oil phase in the air or at the time of touching a target surface.
DETAILED DESCRIPTION OF THE INVENTION
The active insecticidal composition of the present invention includes an aqueous phase and an oil phase. An active insecticidal ingredient that is soluble in oil and substantially insoluble in water dissolves in the oil phase. The active insecticidal composition of the invention forms an oil-free emulsion of limited stability. An emulsion made in accordance with the invention should be considered as of limited stability if it is virtually evident that at least one begins to separate in fifteen seconds from the end of vigorous manual agitation in a bottle or other closed container. An oil-free emulsion that has oil and water phases (or, as an equivalent term, a water-in-oil emulsion) is a type of emulsion in which the oil phase is the continuous phase and the aqueous phase is the phase embedded or discontinuous. Since the oil-free emulsion of this invention has limited stability, the aqueous phase and the oil phase of the composition are usually separated during storage, at least partially. When the two phases of the active insecticidal composition of the invention are mixed together, for example, by stirring or stirring in a container containing the composition, an emulsion without oil is formed, which is substantially free of foam but which is also homogeneous or almost homogeneous When this emulsion is sprayed from the container, the aqueous phase separates from the oil phase at least partially and preferably completely, while the emulsion continues to travel through the air or rapidly at the time of touching the target surface. Typically, the aqueous phase is separated within about 10 seconds after the emulsion has been sprayed. Preferably, the aqueous phase is separated in about 5 seconds, and most preferably, the aqueous phase is separated immediately after the emulsion has been sprayed. As a result, there is no unpleasant milky residue remaining which characterizes the appearance of an emulsion on the target surface. Many insects have a dermatosque ueleto made mainly of chitin, which has a water repellent surface. The water easily spreads from the chitin surfaces without much penetration into the pores of the insect surfaces. In the present invention, the aqueous phase is separated from the oil phase and runs, leaving the oil phase and its active insecticidal ingredient, dissolved, on the surface of the insect. The oil phase moistens the surface, resulting in the active insecticidal ingredient carried in the oil phase penetrating more effectively into the pores of the surface. Accordingly, the composition of this invention is highly effective in killing insects. Preferably, a surfactant is present in the composition in an amount that is effective to provide an emulsion of limited stability. If the amount of surfactant present is excessive, the emulsion may become too stable and take on an excessively milky appearance. That is, the aqueous phase and the oil phase will not separate sufficiently after spraying. If the amount of surfactant present is not sufficient, the composition can not form an emulsion, at all. Typically, the amount of surfactant is from about 0.03% to about 0.10%, preferably from about 0.05% to about 0.10%, by weight, based on the total weight of the composition. All nonionic, anionic, and cationic surfactants can be used in the compositions of this invention, provided the surfactant can cause the formation of an oil-free emulsion by manually stirring the composition in a bottle or can. Preferably, the surfactant has a hydrophilic / lipophilic balance (hereinafter referred to as an "HLB") of between about 3 and about 9. If the surfactant has an HLB greater than about 9, by stirring an emulsion can be formed without water, instead of an emulsion without oil. If the surfactant has an HLB less than about 3, it becomes difficult to form an emulsion in situ by stirring the container while maintaining the composition. Nonionic surfactants are the preferred surfactants used in the compositions of the present invention, since they generally exhibit low toxicity to non-target humans and animals and are non-corrosive. Cationic surfactants tend to be corrosive in commercially common metal containers, typically used to contain insecticidal sprays. The anionic surfactants can cause nasal irritation, if they breathe and can also cause the formation of foam. Examples of suitable nonionic surfactants include long chain fatty acid esters of polyhydroxy compounds such as glycol, glycerol, and sorbitol esters of oleic, stearic, palmitic and lauric acids.; polyethoxylated fatty alcohols having from 2 to 9 ethylene oxide units; and polyethoxylated nonyl phenols having from 2 to 9 ethylene oxide units. Preferred nonionic surfactants are sorbitan mono-oleate, and sorbitan monostearate, which are commercially available as Span® 80, Span® 60, and Span® 40, respectively, from ICI Specialty Chemicals. The very preferred nonionic surfactant for the composition of this invention is sorbitan mono-oleate. The oil phase of the composition of this invention contains a hydrocarbon solvent. The amount of the solvent present in the composition must be effective to dissolve the active ingredient and form an emulsion without oil. Typically, the hydrocarbon solvent is present in the composition in an amount of from about 0.5% to about 40% and preferably from about 5% to about 30% by weight, based on the total weight of the composition. Examples of suitable hydrocarbon solvents include aliphatic, aromatic and naphthenic solvents, and mixtures thereof. Examples of suitable aliphatic hydrocarbons include isoparaffinic and normal paraffinic solvents such as those commercially available from Exxon Chemicals of Houston, Texas under the trade names of ISOPAR® and NORPAR®. Examples of suitable aromatic solvents include benzene, toluene and xylene. Examples of suitable naphthenic solvents include dearomatized and naphthenic aromatics containing isoparaffins. Naphthenic solvents are generally commercially available as mixtures of naphthenic, normal paraffinic and / or isoparaffinic solvents. Examples of suitable naphthenic solvents that are commercially available include EXXSOL® D-40, D-60, D-80, D-110, and D-130 from Exxon Chemicals, Houston, Texas. A preferred hydrocarbon solvent for use in the present invention is a mixture of normal naphthenic and paraffinic solvents, commercially available as EXXSOL® D-60. A co-solvent that is soluble in both the aqueous phase and the oil phase can also be added to the composition of this invention. The co-solvent assists the solubilization of the active insecticidal ingredient in the oil phase and also accelerates the breakdown of the emulsion. Typically, the amount of the co-solvent present is from about 1% to about 5% by weight, based on the total weight of the composition. If the amount exceeds approximately 5%, the emulsion may not be formed. Examples of suitable co-solvents include alcohols such as methanol, ethanol, propanol and isopropanol. As described above, the composition of the present invention contains at least one active insecticidal ingredient in an amount sufficient to provide insecticidal activity. Any conventional active ingredient that is insoluble in water and soluble in the hydrocarbon solvent can be used. Examples of suitable active ingredients include, but are not limited to, natural pyrethrins, synthetic pyrethroids such as permethrin, cypermethrin, deltamethrin, alphamethrin, cyphenothrin, fenvolerate, allethrin, tetramethrin, resmethrin, bioresmethrin, d-trans-allethrin, and phenothrin, pyrethroid halogenated and cyano-pyrethroid. Typically, the active ingredient is present in the compositions of the present invention in an amount of from about 0.20% to about 2%, and preferably from about 0.10% to about 1% by weight, based on the total weight of the composition. A synergist for the active ingredient in the compositions of this invention may also be included in conventional amounts. Examples of suitable synergists include piperonyl butoxide and N-octyl-bicycloheptane-dicarboximide. The water forming the aqueous phase of the composition of the invention must be present in an effective amount to form an oil-free emulsion of limited stability and to facilitate spraying. When the composition is sprayed from a container, the water works as a filler to add volume to the sprayed product. Typically, water is present in the composition in an amount of fabout 30% to about 70% and preferably fabout 40% to about 70% by weight, based on the total weight of the composition. The active insecticidal composition of the present invention can be combined with a suitable propellant to form an aerosol formulation. Examples of suitable propellants include compressed gas propellants such as nitrogen, carbon dioxide, and nitrous oxide; liquefied gas propellants such as fluorinated and chlorinated hydrocarbons, dimethyl ether, vinyl chloride; saturated hydrocarbons such as propane, butane, and sobutane, isopentane, and mixtures thereof; and mixtures of liquefied gases and compressed gases. In order to reduce environmental pollution, it is preferred to employ liquefied saturated hydrocarbons as the propellant. Typically, the hydrocarbon propellant is present in the composition of this invention in an amount of from about 8% to about 50%, and preferably from about 5% to about 30% by weight, based on the total weight of the composition. Other ingredients that may be part of the composition of the present invention include fragrance in conventional amounts to mask the unpleasant odor of active ingredients and corrosion inhibitors such as nitrite, sodium benzoate, and mixtures thereof in conventional amounts to inhibit corrosion of metal containers, in which the composition is usually contained. The present invention will now be illustrated with the following non-limiting examples.
EXAMPLE
An active insecticidal composition that can form an oil-free emulsion of limited stability was prepared with the following ingredients:
Ingredients Percent in Weight Pyrethrin 20% 1,000 Permethrin 90% 0.222 Piperonyl Butoxide 0.500 Sorbitan Mono-Oleate 0.050 Fragrance 0.228 Isopropanol 1,000 EXXSOL® D-60 29,000 Sodium Nitrite 0.090 Water 59.910 Propellant A-91 8,000
The A-91 propellant is a conventional propellant containing 70% propane and 30% isobutane. The composition was prepared by dissolving the 20% pyrethrin, 90% permethrin, piperonyl butoxide, sorbitan mono-oleate, fragrance, and isopropanol in EXXSOL® D-60 to form a solvent intermediate. The sodium nitrite was dissolved in water to form a water intermediate. The water intermediate was then added to an aerosol container, followed by the solvent intermediate. Then, a valve was placed in the container and held. The vessel was then pressurized with the A-91 propellant. The vessel was then stirred to form an oilless emulsion of limited stability. Immediately afterwards, the composition was sprayed from the container to a target surface. It was observed that when the spray touched the target surface, the aqueous phase separated from the oil phase almost immediately. As a result, there were no unpleasant milky spots on the target surface. Since the present invention has been described with respect to what are currently considered the preferred embodiments, it should be understood that the invention is not limited to the embodiments described. Otherwise, the invention is intended to cover the various equivalent modifications and formulations included within the scope and spirit of the appended claims. The scope of the following claims has to be in accordance with the broadest interpretation in order to encompass such modifications and equivalent formulations and functions.
INDUSTRIAL APPLICABILITY
Insecticidal spray compositions have immediate utility in the control of insect pests. The active insecticidal composition of the invention has the additional, industrially desirable application of providing a composition having a reduced concentration of volatile petroleum products, while remaining both suitable for spraying through conventional means and an effective insect spraying annihilator. .
Claims (19)
- CLAIMS 1 .- An active insecticidal composition that forms an emulsion if oil of limited stability, comprising: an aqueous phase comprising water; an oil phase comprising a hydrocarbon solvent and at least one active insecticidal ingredient; and an amount of an effective surfactant to form an oil-free, non-foaming emulsion; whereby when the emulsion is formed inside and then sprayed from a container, the aqueous phase separates at least partially from the oil phase in the air or at the time of touching the target surface.
- 2. The active insecticidal composition according to claim 1, wherein said surfactant is present in an amount of about 0.03% to about 0.10% by weight, based on the total weight of the composition.
- 3. The active insecticidal composition according to claim 2, wherein said surfactant is present in an amount from about 0.05% to about 0.10%.
- 4. - The active insecticidal composition according to claim 1, wherein said surfactant agent has an HLB of between about 3 and about 9.
- The active insecticidal composition according to claim 4, wherein said surfactant is selected from the group consisting of nonionic, anionic and cationic surfactants.
- 6. - The active insecticidal composition according to claim 5, wherein said surfactant is a nonionic surfactant.
- 7. The active insecticidal composition according to claim 6, wherein said surfactant is selected from the group consisting of glycol, glycerol, and sorbitol esters of oleic, stearic, palmitic and lauric acids, polyethoxylated fatty alcohols having 2 to 9 units of ethylene oxide and polyethoxylated nonylphenols having from 2 to 9 units of ethylene oxide.
- 8. The active insecticidal composition according to claim 6, wherein said surfactant is selected from the group consisting of sorbitan mono-oleate, sorbitan monostearate and sorbitan monopalmitate.
- 9 - The active insecticidal composition according to claim 1, wherein said hydrocarbon solvent is selected from the group consisting of aliphatic, aromatic and naphthenic solvents, and mixtures thereof.
- 10. The active insecticidal composition according to claim 1, wherein said composition further comprises a co-solvent.
- 11. The active insecticidal composition according to claim 10, wherein said co-solvent is an alcohol.
- 12. The active insecticidal composition according to claim 1, wherein said active ingredient is selected from the group consisting of natural pyrethroids, synthetic pyrethroids, halogenated pyrethroids and cyano-pyrethroids.
- 13. The active insecticidal composition according to claim 1, wherein it further comprises a synergist for said active ingredient.
- 14. The active insecticidal composition according to claim 13, wherein said synergist is selected from the group consisting of piperonyl butoxide and N-octyl-bicycloheptane-dicarboximide.
- 15. The active insecticidal composition according to claim 1, wherein it further comprises a propellant.
- 16. The active insecticidal composition according to claim 15, wherein said propellant is selected from the group consisting of liquefied saturated hydrocarbons and mixtures thereof.
- 17. The active insecticidal composition according to claim 1, wherein said composition further comprises a fragrance.
- 18. The active insecticidal composition according to claim 1, wherein said composition further comprises a corrosion inhibitor.
- 19. The active insecticidal composition according to claim 18, wherein said corrosion inhibitor is selected from the group consisting of sodium nitrite, sodium benzoate, and mixtures thereof.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US379247 | 1982-05-17 | ||
US37924795A | 1995-01-27 | 1995-01-27 | |
PCT/US1996/000983 WO1996022686A1 (en) | 1995-01-27 | 1996-01-24 | Insecticidally-active composition |
Publications (2)
Publication Number | Publication Date |
---|---|
MX9705678A MX9705678A (en) | 1997-10-31 |
MXPA97005678A true MXPA97005678A (en) | 1998-07-03 |
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