MXPA97007900A - Sanitation composition especially adapted for the treatment of buildings for animal crises - Google Patents
Sanitation composition especially adapted for the treatment of buildings for animal crisesInfo
- Publication number
- MXPA97007900A MXPA97007900A MXPA/A/1997/007900A MX9707900A MXPA97007900A MX PA97007900 A MXPA97007900 A MX PA97007900A MX 9707900 A MX9707900 A MX 9707900A MX PA97007900 A MXPA97007900 A MX PA97007900A
- Authority
- MX
- Mexico
- Prior art keywords
- use according
- chlorides
- solution
- per liter
- composition
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 57
- 230000000249 desinfective Effects 0.000 claims abstract description 19
- 239000002917 insecticide Substances 0.000 claims abstract description 19
- 150000002191 fatty alcohols Chemical class 0.000 claims abstract description 12
- 241001465754 Metazoa Species 0.000 claims abstract description 10
- SXRSQZLOMIGNAQ-UHFFFAOYSA-N glutaraldehyde Chemical compound O=CCCCC=O SXRSQZLOMIGNAQ-UHFFFAOYSA-N 0.000 claims abstract description 9
- QGZKDVFQNNGYKY-UHFFFAOYSA-O ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims abstract description 6
- 239000007864 aqueous solution Substances 0.000 claims abstract description 5
- 150000003839 salts Chemical class 0.000 claims abstract description 5
- 239000011780 sodium chloride Substances 0.000 claims abstract description 5
- 235000019270 ammonium chloride Nutrition 0.000 claims abstract description 4
- 230000000384 rearing Effects 0.000 claims abstract 2
- 239000000243 solution Substances 0.000 claims description 11
- 150000001875 compounds Chemical class 0.000 claims description 10
- 239000000126 substance Substances 0.000 claims description 10
- RLLPVAHGXHCWKJ-HKUYNNGSSA-N (3-phenoxyphenyl)methyl (1R,3R)-3-(2,2-dichloroethenyl)-2,2-dimethylcyclopropane-1-carboxylate Chemical class CC1(C)[C@@H](C=C(Cl)Cl)[C@H]1C(=O)OCC1=CC=CC(OC=2C=CC=CC=2)=C1 RLLPVAHGXHCWKJ-HKUYNNGSSA-N 0.000 claims description 8
- 229960000490 Permethrin Drugs 0.000 claims description 8
- VEXZGXHMUGYJMC-UHFFFAOYSA-M chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 claims description 8
- 150000003242 quaternary ammonium salts Chemical class 0.000 claims description 6
- -1 alkylbenzyl chlorides Chemical class 0.000 claims description 4
- 230000001488 breeding Effects 0.000 claims description 4
- 125000004432 carbon atoms Chemical group C* 0.000 claims description 3
- FARBQUXLIQOIDY-UHFFFAOYSA-M dimethyl(dioctyl)azanium;chloride Chemical compound [Cl-].CCCCCCCC[N+](C)(C)CCCCCCCC FARBQUXLIQOIDY-UHFFFAOYSA-M 0.000 claims description 3
- IAYPIBMASNFSPL-UHFFFAOYSA-N oxane Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims description 3
- CNDHHGUSRIZDSL-UHFFFAOYSA-N 1-chlorooctane Chemical compound CCCCCCCCCl CNDHHGUSRIZDSL-UHFFFAOYSA-N 0.000 claims description 2
- 150000001348 alkyl chlorides Chemical class 0.000 claims description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 2
- 235000019441 ethanol Nutrition 0.000 claims description 2
- 150000003505 terpenes Chemical class 0.000 claims description 2
- 235000007586 terpenes Nutrition 0.000 claims description 2
- 150000003841 chloride salts Chemical class 0.000 claims 2
- 125000001931 aliphatic group Chemical class 0.000 claims 1
- NLXLAEXVIDQMFP-UHFFFAOYSA-N ammonia chloride Chemical class [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 claims 1
- 125000003118 aryl group Chemical class 0.000 claims 1
- 230000015572 biosynthetic process Effects 0.000 claims 1
- 238000003786 synthesis reaction Methods 0.000 claims 1
- 230000002194 synthesizing Effects 0.000 claims 1
- 230000000749 insecticidal Effects 0.000 description 19
- 230000000844 anti-bacterial Effects 0.000 description 12
- 239000000047 product Substances 0.000 description 10
- 230000000694 effects Effects 0.000 description 5
- 230000003253 viricidal Effects 0.000 description 5
- 150000001299 aldehydes Chemical class 0.000 description 4
- 238000010790 dilution Methods 0.000 description 4
- 230000000855 fungicidal Effects 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- 239000003899 bactericide agent Substances 0.000 description 3
- 230000015556 catabolic process Effects 0.000 description 3
- 239000000470 constituent Substances 0.000 description 3
- 231100000078 corrosive Toxicity 0.000 description 3
- 231100001010 corrosive Toxicity 0.000 description 3
- 230000004059 degradation Effects 0.000 description 3
- 238000006731 degradation reaction Methods 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 241000238631 Hexapoda Species 0.000 description 2
- 230000032683 aging Effects 0.000 description 2
- UIERETOOQGIECD-ARJAWSKDSA-N angelic acid group Chemical group C(\C(\C)=C/C)(=O)O UIERETOOQGIECD-ARJAWSKDSA-N 0.000 description 2
- 238000003975 animal breeding Methods 0.000 description 2
- 150000001805 chlorine compounds Chemical class 0.000 description 2
- 230000000875 corresponding Effects 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000004177 patent blue V Substances 0.000 description 2
- 125000001453 quaternary ammonium group Chemical group 0.000 description 2
- 239000004172 quinoline yellow Substances 0.000 description 2
- 239000004094 surface-active agent Substances 0.000 description 2
- 230000002588 toxic Effects 0.000 description 2
- 231100000331 toxic Toxicity 0.000 description 2
- 239000000080 wetting agent Substances 0.000 description 2
- MBEVSMZJMIQVBG-UHFFFAOYSA-N 2-(hydroxymethyl)guanidine Chemical compound NC(N)=NCO MBEVSMZJMIQVBG-UHFFFAOYSA-N 0.000 description 1
- UDHXJZHVNHGCEC-UHFFFAOYSA-N Chlorophacinone Chemical compound C1=CC(Cl)=CC=C1C(C=1C=CC=CC=1)C(=O)C1C(=O)C2=CC=CC=C2C1=O UDHXJZHVNHGCEC-UHFFFAOYSA-N 0.000 description 1
- 235000007516 Chrysanthemum Nutrition 0.000 description 1
- 240000005250 Chrysanthemum indicum Species 0.000 description 1
- 235000005986 Chrysanthemum x morifolium Nutrition 0.000 description 1
- 241001633993 Cineraria Species 0.000 description 1
- SDIXRDNYIMOKSG-UHFFFAOYSA-L Disodium methyl arsenate Chemical compound [Na+].[Na+].C[As]([O-])([O-])=O SDIXRDNYIMOKSG-UHFFFAOYSA-L 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- 235000008331 Pinus X rigitaeda Nutrition 0.000 description 1
- 235000011613 Pinus brutia Nutrition 0.000 description 1
- 241000018646 Pinus brutia Species 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 241000589517 Pseudomonas aeruginosa Species 0.000 description 1
- 229940055023 Pseudomonas aeruginosa Drugs 0.000 description 1
- 241000700605 Viruses Species 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- VHUUQVKOLVNVRT-UHFFFAOYSA-N ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
- 150000001450 anions Chemical class 0.000 description 1
- 230000003042 antagnostic Effects 0.000 description 1
- 239000005557 antagonist Substances 0.000 description 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
- 238000006065 biodegradation reaction Methods 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000004568 cement Substances 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 230000000295 complement Effects 0.000 description 1
- 239000000645 desinfectant Substances 0.000 description 1
- 201000010099 disease Diseases 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- XWBDWHCCBGMXKG-UHFFFAOYSA-N ethanamine;hydron;chloride Chemical class Cl.CCN XWBDWHCCBGMXKG-UHFFFAOYSA-N 0.000 description 1
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 1
- 238000009313 farming Methods 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 239000000417 fungicide Substances 0.000 description 1
- 239000001046 green dye Substances 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 238000009533 lab test Methods 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 230000003000 nontoxic Effects 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 239000002304 perfume Substances 0.000 description 1
- 230000002688 persistence Effects 0.000 description 1
- 238000005191 phase separation Methods 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 230000036186 satiety Effects 0.000 description 1
- 235000019627 satiety Nutrition 0.000 description 1
- 230000000087 stabilizing Effects 0.000 description 1
- 230000002195 synergetic Effects 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 230000002110 toxicologic Effects 0.000 description 1
- 231100000027 toxicology Toxicity 0.000 description 1
- 239000000273 veterinary drug Substances 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 230000003612 virological Effects 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
Abstract
The present invention relates to: A disinfectant composition in aqueous solution specially adapted for the treatment of buildings for the rearing of animals, characterized in that it contains, in weight proportions, between 1 and 20% of monoaldehydes or dialdehydes, especially glutaraldehyde, between 3 and 35% of salts, especially quaternary ammonium chlorides, between 1 and 15% of ethoxylated fatty alcohol, and between 0.5 and 15% of an insecticide agent chosen among the pyrethrinoids of
Description
COMPOSITION DISINFECTANT SPECIALLY ADAPTED FOR THE TREATMENT OF BUILDINGS FOR ANIMAL FARMING The present invention relates to a disinfectant composition in aqueous solution specially adapted for the treatment of buildings for animal husbandry during the so-called periods of "sanitary vacuum" that separate each batch of animals. Currently on the market are numerous disinfectant compositions whose purpose is the cleaning of the premises in the case of the industrial breeding of animals. To give satiety, such compositions must have a remarkable disinfectant activity, that is, a bactericidal, virucidal and fungicidal action; in addition, they must be chemodegradable or biodegradable, and not be toxic and not very corrosive. In order to satisfy these different criteria, it has already been proposed, in accordance with publication FR-A-87 15 212, a composition containing, by weight, between 3 and 35% of quaternary ammonium salts, between 1 and 20% of straight chain di aldehyde, especially glutaraldehyde, and between 1 and 15% of ethoxy side fatty alcohols. This composition, in use, has proved to be particularly active, easily eli unleable and without danger to human health. The bactericidal, virucidal and fungicidal qualities of quaternary ammonium and glutaraldehyde are well known for a long time. In the aforementioned disinfected composition, the fatty alcohols act as wetting and solubilizing agents capable of improving the "stability" of the solution and allowing the increase in the proportion of active products. The combination of quaternary ammonium salts of glutaraldehyde and ethoxylated fatty alcohols therefore makes it possible to obtain, in aqueous solution, very concentrated disinfectant compositions with a very broad spectrum of disinfectant activity and having, in particular, a very remarkable directed activity due to the excellent Tenoactivity of quaternary ammoniums. By way of example, the following composition proved to be particularly active: dideei chloride ldimeti lamonium 18.75 g
Dioctyl chloride ldimeti lamonium 18.75 g
Chloride of oct i ldeci Idi eti lamonio 37.50 g Alkyl Chloride < C14 50% - C12 40% - C16 10%) dimet i 1ben i 1 ammonium 50 g
Glutaraldehldo 62.50 g
Terpinol 20 g
Pine essence 20 g Fatty alcohols ethoxylated with 10 moles of ethylene oxide and 90% active matters. 40 g Angelic Green Dye < E 131 + E 104) 1 g
Water q .s .p. 1 1 i tro
Despite its proven advantages, this disinfectant composition has the drawback of not having any insecticidal action and therefore must be combined with a complementary treatment with the help of an insecticide product to obtain a complete sanitary "action". These operations represent an economic and material effort (number of operations, exposure of personnel, lengthening of period of "sanitary vacuum" of animal breeding sites). Therefore, and despite manufacturers' recommendations, users are sometimes tempted to mix in the course of the same treatment disinfectant specialties that do not have insecticidal action and insecticidal specialties that have no bactericidal or virucidal action. The mixtures made in this way, however, contact substances which are not necessarily compatible with each other and can cause poisoning-type accidents. In addition, studies that allow manufacturers to determine the efficacy of their product do not systematically take into account interactions that may appear when these products are associated with another specialty and can not guarantee that products mixed in this way retain their activity and stability. . Therefore, it would be desirable to be able to have a polyvalent specialty effectively associating disinfectant properties (bactericides, viricides and fungicides) and insecticidal properties. In spite of this obvious need, up to now it had not been possible to collect the necessary active substances in an active form, which is iscible in water and in suitable concentrations to obtain the essential efficacy for a single dose of use. The object of the present invention is to satisfy this need by proposing a composition adapted to the treatment of animal breeding buildings, chemically stable which has a high efficacy both insecticidal and bactericidal, virucidal and fungicidal and in parallel non-toxic for the intended use. and slightly corrosive in relation to exposed materials (especially metals). According to the present invention, this composition is characterized in that it contains, in proportions by weight, between 1 and 20% of onoaldehydes or dialdehydes, especially glutaraldehyde, between 3 and 35% of salts, especially quaternary ammonium chlorides, between 1 and 15 % of ethoxylated fatty alcohol and between 0.5 and 15% of an insecticide agent chosen among the synthetic pyrethrinoids, ie the analogs of pyrethrin which is a known insecticide itself constituted by toxic principles extracted from flowers and aerial parts of pi retre (Chrysanthemum Cineraria Folium). We observed that, surprisingly, it was possible, from the aforementioned known disinfectant composition, object of document FR-A-87 15 212 and acting on the nature and proportions of the solvents and surfactants employed, to obtain a stable and effective polyvalent composition thanks to the incorporation of a specific insecticide agent. According to the present invention, this insecticidal agent can advantageously be constituted by an isomer or a mixture of isomers of permethrin, particularly a mixture of approximately 25% cis isomer and about 75% trans isomer. Permethrin or <; l, RS) cis, trans (dichloro-2,2 vinyl) -3 dimethyl-2,2-cyclopropane carboxylate of phenoxy-3 benzyl is a pyrethrinoid with a broad spectrum of activity that is distinguished by a good persistence and whose effectiveness allows ensure insecticidal protection when used in low doses. The composition according to the present invention can advantageously contain about 20 g of synthetic pyrethrinoids and especially of permethrin by solution sol. According to another feature of the invention, the composition contains between 0.2 and 40% of terpene extacto and especially terpinol. The addition of terpinol in the composition according to the present invention is especially advantageous taking into consideration the fact that this compound, which has important bactericidal qualities, is at the same time perfume. By way of example, 100 g of terpinol per liter of solution can be used. According to another feature of the present invention, the composition contains essentially, per liter of solution, 60 g of ethoxylated fatty alcohols, consisting of ethoxylated compounds with 11 moles of ethyl alcohol and 45% of active substance. These fatty alcohols function as wetting and solubilizing agents. It is also possible, advantageously, to use, as quaternary ammonium salts, salts largely similar to those contained in the aforementioned disinfectant composition of document FR-A-87 15 212, that is, dialkyl ethylammonium chlorides and / or chlorides of alq? ilbencildi eti lamonio whose alkyl radicals contain between 8 and 16 carbon atoms. According to another characteristic of the invention, the composition essentially contains, per liter of solution, 125 g of quaternary ammonium salts constituted by a mixture of didecyl chloride, imidemmonium chloride, dioctyldimethyl ammonium chloride, octyl chloride, and the like. The Idimet and the anion and chlorides of alkyldimethylbenzylammonium, the latter being constituted by a mixture of approximately 50% by weight of C14 compounds, 40% by weight of C12 compounds and 10% by weight of C16 compounds. According to another feature of the present invention, the composition contains essentially 62.5 g of glutaraldehyde per liter of solution. The composition according to the present invention can and may contain other additives, such as a dye, especially a green dye. By way of example, the following composition proved to be especially advantageous, in uses dideci ldimeti lamonium chloride 18.75 g
Dioctyl dimethyl ammonium chloride 18.75 g
Chloride of octi ldeci ldimeti lamonio 37.50 g
Alkydimether Chloride Ibencylammonium (C14 alkyl 50% -C12 40% - C16 10%) 50 g Blutaraldehyde 62.50 g
Permethrin (cis / trans isomer: 25% / 75%) 20 g Ethoxylated fatty alcohols with 11 moles of ethylene oxide and 45% of active substances. 60 g Terpinol 100 g
Angelic green coloring (E131 - E104) 0.020 g
Water de ineral ized q.s.p. 1 liter
The properties of the composition object of the present invention could be verified by the experimental tests described below: 1) INSECTICIDE EFFICACY Two tests were carried out in order to evaluate the insecticidal power of the composition in accordance with the
> present invention. The performance of such tests proved to be indispensable, taking into consideration the fact that if the insecticidal properties of the pyrethrinoids are well known per se, it was not evident that, within the composition, no antagonists could be produced or "entrapment" phenomenon. of active matters by the other constituents. a) Laboratory test This test was carried out in accordance with the "Protocole exp rimental destiné á établir, en laboratoire, l'efficacité d'une spécialité insecticide" (Experimental protocol whose purpose is to establish, in the laboratory, the efficacy of a specialty insecticide) (Center National d'Etudes Vétérinai res et Al imentai res) (National Center for Veterinary and Food Studies) and made it possible to verify the efficacy of a composition with the composition according to the present invention on surfaces of a different nature (wood, cement and metal). The results, which take into consideration mortality percentages obtained with flies, appear in figure la (corresponding to mortality without treatment) and in figure Ib (corresponding to mortality after treatment).
From the first 20 minutes of exposure, the efficacy is optimal. b) Tests carried out in the field Only the natural conditions of use make it possible to evaluate the actual effectiveness of an insecticide. In fact, the remanence of the treatment is an important quality criterion for this type of product. This remanence is influenced by the stability and resistance of the insecticide on the surfaces to the extent that the latter acts by contact with the insect. The contact with the insect is in turn influenced by the natural fouling of the buildings dedicated to the cria. of animals with the passage of time. The test was carried out in accordance with method No. 107: "Methodological approach for the processing of insecticide products destined to lutter against the mouches des étables dans les lacaux d'élevages d'animaux domestiques" (Test method for practical effectiveness of insecticide products whose purpose is to fight against flies in stables in breeding premises of domestic animals) established by the members of the Coission des Essais Biologiques de l'Association Nationale pour la Protection des Plantes (Commission for Biological Tests) of the National Association for the Protection of Plants). Held the summer, the trial consisted in the comparison of the variations of the population of flies in the buildings dedicated to the breeding of animals in the course of the 3 months after the treatment. The test was carried out both in an untreated building and in a building treated by the composition in accordance with the present invention and in a building treated with a known insecticide for positive control. The results obtained appear in figure 2. CONCLUSION: These results show that the composition according to the present invention is equally effective as a product known exclusively as an insecticide. 2) BACTERICIDE AND VIRICIDE EFFICACY a) Bactericide Preliminary tests allowed to verify that the substances active responsible for bactericidal activity retain their potency. The synergistic association of the mixture of aqueous ammonia and aldehyde which is a characteristic of the above disinfectant composition according to the document FP-A-87 15 212 is not inhibited within the framework of the composition according to the present invention. . This control was carried out by comparing the CMB (minimum bactericidal concentrations) obtained in the Pseudomonas aeruginosa strain in the presence of pure water at 30 ° C (method: by icroplates in accordance with AFNOR NF T 72-170). Four variants of the composition according to the present invention were tested (variations in the proportions of surfactants and co-solvents). RESULTS: For each trial (including the previous disinfectant composition), Bactericidal Minimum Concentrations were obtained for dilutions less than or equal to 0.125%. CONCLUSION: Bactericidal efficacy is maintained compared to the previous approved disinfectant composition for use at 0.5% dilution on e to Pseudomas aeruginosa; the use of the composition according to the present invention is foreseen for a dilution of 2%. b) VIRICIDAL The test was carried out by micromanagement on the virus of the disease of Talfan (Picornaevirus type 1), well known for its resistance to disinfectants and which constitutes for this reason the factor limiting the dilution of use. RESULTS: The composition according to the present invention, diluted at 2%, allows to obtain a reduction of at least 3 Log of the viral titer, in accordance with the requirements of the Laboratoire des Medicamente Vétérinaires (Laboratory of Veterinary Drugs) in relation to the disinfectant of agricultural use. 3) CHEMICAL STABILITY The stability study of the composition includes the control of the appearance of the product, the measurement of the pH and the dosage of the active substances. The study is carried out on samples stored in polypropylene bottles, in a bath at a temperature of 37 ° C, in order to have an accelerated aging profile. The data presented below correspond to batches stored at 37 ° C for more than 3 months, a) Appearance of the samples absence of precipitates absence of phase separation of the constituents stable coloration.
That is, an aspect without change after 3 months at 37 ° C. b) Stability of the aldehydes The stability at a temperature of 37 ° C of the aldehydes is shown in Figure 3. No significant degradation is observed after 99 days at a temperature of 37 ° C. c) Stability of quaternary ammoniums The stability at 37 ° C of quaternary ammonium is shown in Figure 4. No significant degradation is observed after 99 days at a temperature of 37 ° C. d) Stability of permethrin The stability at 37 ° C of permethrin appears in Figure 5. No significant degradation is observed after 99 days at a temperature of 37 ° C. e) Variations of the pH The pH evolution at a temperature of 37 * C appears in figure 6. The pH decreases slightly after 2 months f) Comments The graphs mentioned above correspond to the results of the dosages made on six different batches of the composition according to the present invention. These lots contain some variations among them in terms of the percentages of excipients. It can be seen that the active substances successfully resist the aging conditions at 37 ° C for at least 3 months. 4) TOXICOLOGICAL ASPECT The different constituents of the composition according to the present invention do not present a particular danger in the expected dose of use (2% in aqueous dilution). 5) CORROSIVE ACTION OF THE COMPOSITION In the doses of use, the composition presents no particular risk in relation to the materials exposed to the treatments.
Claims (11)
- CLAIMS 1. The use for the treatment of buildings for the rearing of animals, particularly during the periods known as "sanitary vacuum" that separate each batch of animals, from a disinfectant composition in aqueous solution containing, in proportions by weight, between 1 and 20% of onoaldehydes or dialdehldoß, especially glutaraldehyde, between 3 and 35% of salts, especially quaternary ammonium chlorides, between 1 and 15% of ethoxylated fatty alcohols, and between 0.5 and 15% of an insecticide agent chosen among the pyrethrinoids of synthesis.
- 2. The use according to claim 1, characterized in that the insecticidal agent constitutes an isomer or a mixture of isomers of permethrin.
- 3. The use according to claim 2, characterized in that the insecticidal agent contains approximately 25% cis isomer and 75% trans isomer.
- 4. The use according to any of the rei indications 1 to 3, characterized in that it contains between 0.2 and 40% terpene extract, especially terpinal.
- 5. The use according to any of claims 1 to 4, characterized in that the quaternary ammonium salts are dialkydimetiimmonium chlorides and / or alkylimethylbenzylchlorides, the alkyl radicals contain between 8 and 16 carbon atoms. .
- 6. The use according to claim 5, characterized in that it contains essentially, per liter of solution, 125 g of quaternary ammonium salt constituted by a mixture of d idee and Idimet chloride, of dioctyldimethylammonium chloride, of octylchloride chloride. Idimet and ammonium chlorides and Ibenci lamanium alkyl chlorides, the latter consisting of a mixture of approximately 50% by weight of C14 compounds, 40% by weight of C12 compounds and 10% by weight of C16 compounds. The use according to any of claims 1 to 6, characterized in that it contains essentially 62.5 g of glutaraldehyde per liter of solution. 8. The use according to any of claims 1 to 7, characterized in that it contains essentially 20 g of synthetic pyrethrinoids and especially of permethrin per liter of solution. 9. The use according to any of the above indications 1 to 8, characterized in that it contains essentially, per liter of solution, 60 g of ethazylated fatty alcohols, constituted by ethoxylated compounds with 11 moles of ethyl alcohol and 45% of active substance. 10. The use according to any of claims 1 to 9, characterized in that it contains essentially 100 g of terpinol per liter of solution. 11. The disinfectant composition in aqueous solution specially adapted for the treatment of buildings for the breeding of animals, characterized because it contains in weight proportions between 1 and 20% of onoaldehydes to good dialdehydes, especially glutaraldehyde, between 3 and 35% of dialki chlorides. limeti lamonia and / or alkylbenzyl chlorides Idimethylammonium, the alkyl radicals contain between 8 and 16 carbon atoms, between 1 and 15% of ethoxylated fatty alcohols consisting of ethoxylated compounds with 11 moles of ethylene oxide and 45% of active substance, and between 0.5 and 15% of an insecticide agent chosen among the synthetic pyrethrinoids, this composition is free of salts of aliphatic acids or aromatic hydroxylates.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR9612616 | 1996-10-16 | ||
FR9612616A FR2754425B1 (en) | 1996-10-16 | 1996-10-16 | DISINFECTANT COMPOSITION IN PARTICULAR SUITABLE FOR THE TREATMENT OF LIVESTOCK |
Publications (2)
Publication Number | Publication Date |
---|---|
MX9707900A MX9707900A (en) | 1998-08-30 |
MXPA97007900A true MXPA97007900A (en) | 1998-11-12 |
Family
ID=
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JP6933983B2 (en) | Vitamin E-containing isooxazoline solution for use with sanitized drinking water | |
US10959429B2 (en) | Disinfectant formulation | |
RU2302858C2 (en) | Parasiticidal compositions and methods for their application | |
EP3927163A1 (en) | A method and composition for insect repellency using aversive agent | |
CN102334501A (en) | Preparation and application of multifunctional atomization agent for controlling pests | |
US20040253287A1 (en) | Environmentally safe insecticides | |
US5932615A (en) | Disinfecting composition especially suitable for the treatment of livestock buildings | |
CN102318639A (en) | Preparation and application with compound Alevaire of sterilization and insecticidal function | |
US6103763A (en) | Methods of killing insects | |
CN102334502A (en) | Preparation and application of multifunctional atomization agent for controlling pests in sealed container | |
US9609864B2 (en) | Disinfectant formulation | |
US10638753B2 (en) | Disinfectant formulation | |
US10405544B2 (en) | Disinfectant formulation | |
KR102050708B1 (en) | Composition for disinfection and acaricide, and method for controlling of red mite using the same | |
CN102210300A (en) | Preparation and application of multifunctional atomizing agent for preventing and controlling pests of inspection and quarantine system | |
US10111425B2 (en) | Disinfectant formulation | |
US11589581B2 (en) | Disinfectant formulation | |
US6740319B2 (en) | Chemical attractants for yellowjacket wasps | |
MXPA97007900A (en) | Sanitation composition especially adapted for the treatment of buildings for animal crises | |
CN113854294A (en) | Disinfectant composition for musk deer breeding houses as well as preparation method and application of disinfectant composition | |
CA2141761A1 (en) | Ionone disinfectant | |
JP5701097B2 (en) | Terrestrial invertebrate repellent composition | |
RU2816103C1 (en) | Disinfectant with repellent properties "dez garant anti fly" and method for production thereof | |
KR20110059060A (en) | Rodent repellent composition | |
US20170238557A1 (en) | Aqueous composition based on natural extracts for cleaning, and as a disinfectant, insect repellent, insecticide and freshener |