DE3531920A1 - Method for combating ectoparasites in goats - Google Patents
Method for combating ectoparasites in goatsInfo
- Publication number
- DE3531920A1 DE3531920A1 DE19853531920 DE3531920A DE3531920A1 DE 3531920 A1 DE3531920 A1 DE 3531920A1 DE 19853531920 DE19853531920 DE 19853531920 DE 3531920 A DE3531920 A DE 3531920A DE 3531920 A1 DE3531920 A1 DE 3531920A1
- Authority
- DE
- Germany
- Prior art keywords
- dimethyl
- cyclopropane
- phenoxy
- cyano
- carboxylic acid
- 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.)
- Withdrawn
Links
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- 238000000034 method Methods 0.000 title claims abstract description 15
- 244000078703 ectoparasite Species 0.000 title claims abstract description 11
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- YATDSXRLIUJOQN-SVRRBLITSA-N (2,3,4,5,6-pentafluorophenyl)methyl (1r,3s)-3-(2,2-dichloroethenyl)-2,2-dimethylcyclopropane-1-carboxylate Chemical compound CC1(C)[C@H](C=C(Cl)Cl)[C@H]1C(=O)OCC1=C(F)C(F)=C(F)C(F)=C1F YATDSXRLIUJOQN-SVRRBLITSA-N 0.000 claims description 3
- OLKWYZYVQYPFIM-UHFFFAOYSA-N 3-[2-chloro-2-(4-chlorophenyl)ethenyl]-2,2-dimethylcyclopropane-1-carboxylic acid Chemical compound OC(=O)C1C(C)(C)C1C=C(Cl)C1=CC=C(Cl)C=C1 OLKWYZYVQYPFIM-UHFFFAOYSA-N 0.000 claims description 3
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- 235000019445 benzyl alcohol Nutrition 0.000 description 1
- 229960002903 benzyl benzoate Drugs 0.000 description 1
- 235000019437 butane-1,3-diol Nutrition 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
- 239000001768 carboxy methyl cellulose Substances 0.000 description 1
- 150000001733 carboxylic acid esters Chemical class 0.000 description 1
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 150000008422 chlorobenzenes Chemical class 0.000 description 1
- 239000008119 colloidal silica Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 235000005822 corn Nutrition 0.000 description 1
- 235000012343 cottonseed oil Nutrition 0.000 description 1
- 239000002385 cottonseed oil Substances 0.000 description 1
- SASYSVUEVMOWPL-NXVVXOECSA-N decyl oleate Chemical compound CCCCCCCCCCOC(=O)CCCCCCC\C=C/CCCCCCCC SASYSVUEVMOWPL-NXVVXOECSA-N 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 230000001804 emulsifying effect Effects 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- LVGKNOAMLMIIKO-QXMHVHEDSA-N ethyl oleate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCC LVGKNOAMLMIIKO-QXMHVHEDSA-N 0.000 description 1
- 229940093471 ethyl oleate Drugs 0.000 description 1
- 229920000159 gelatin Polymers 0.000 description 1
- 239000008273 gelatin Substances 0.000 description 1
- 235000019322 gelatine Nutrition 0.000 description 1
- 235000011852 gelatine desserts Nutrition 0.000 description 1
- 210000004907 gland Anatomy 0.000 description 1
- 230000000762 glandular Effects 0.000 description 1
- 125000005456 glyceride group Chemical group 0.000 description 1
- YQEMORVAKMFKLG-UHFFFAOYSA-N glycerine monostearate Natural products CCCCCCCCCCCCCCCCCC(=O)OC(CO)CO YQEMORVAKMFKLG-UHFFFAOYSA-N 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- SVUQHVRAGMNPLW-UHFFFAOYSA-N glycerol monostearate Natural products CCCCCCCCCCCCCCCCC(=O)OCC(O)CO SVUQHVRAGMNPLW-UHFFFAOYSA-N 0.000 description 1
- 150000002314 glycerols Chemical class 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- FUZZWVXGSFPDMH-UHFFFAOYSA-M hexanoate Chemical compound CCCCCC([O-])=O FUZZWVXGSFPDMH-UHFFFAOYSA-M 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 239000001023 inorganic pigment Substances 0.000 description 1
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
- 229940089456 isopropyl stearate Drugs 0.000 description 1
- 229940067606 lecithin Drugs 0.000 description 1
- 229920005610 lignin Polymers 0.000 description 1
- 230000005923 long-lasting effect Effects 0.000 description 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- XJRBAMWJDBPFIM-UHFFFAOYSA-N methyl vinyl ether Chemical compound COC=C XJRBAMWJDBPFIM-UHFFFAOYSA-N 0.000 description 1
- 239000004530 micro-emulsion Substances 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000019426 modified starch Nutrition 0.000 description 1
- 229940042880 natural phospholipid Drugs 0.000 description 1
- 229920000847 nonoxynol Polymers 0.000 description 1
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical class CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- BARWIPMJPCRCTP-UHFFFAOYSA-N oleic acid oleyl ester Natural products CCCCCCCCC=CCCCCCCCCOC(=O)CCCCCCCC=CCCCCCCCC BARWIPMJPCRCTP-UHFFFAOYSA-N 0.000 description 1
- 229940055577 oleyl alcohol Drugs 0.000 description 1
- XMLQWXUVTXCDDL-UHFFFAOYSA-N oleyl alcohol Natural products CCCCCCC=CCCCCCCCCCCO XMLQWXUVTXCDDL-UHFFFAOYSA-N 0.000 description 1
- 125000001117 oleyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])/C([H])=C([H])\C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- BARWIPMJPCRCTP-CLFAGFIQSA-N oleyl oleate Chemical compound CCCCCCCC\C=C/CCCCCCCCOC(=O)CCCCCCC\C=C/CCCCCCCC BARWIPMJPCRCTP-CLFAGFIQSA-N 0.000 description 1
- 239000004006 olive oil Substances 0.000 description 1
- 235000008390 olive oil Nutrition 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 150000002903 organophosphorus compounds Chemical class 0.000 description 1
- QUANRIQJNFHVEU-UHFFFAOYSA-N oxirane;propane-1,2,3-triol Chemical compound C1CO1.OCC(O)CO QUANRIQJNFHVEU-UHFFFAOYSA-N 0.000 description 1
- 238000007911 parenteral administration Methods 0.000 description 1
- 239000000312 peanut oil Substances 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 150000003904 phospholipids Chemical class 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-N phosphoric acid Substances OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 1
- 235000011007 phosphoric acid Nutrition 0.000 description 1
- 239000001007 phthalocyanine dye Substances 0.000 description 1
- 239000002798 polar solvent Substances 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 239000008389 polyethoxylated castor oil Substances 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920000259 polyoxyethylene lauryl ether Polymers 0.000 description 1
- 235000010483 polyoxyethylene sorbitan monopalmitate Nutrition 0.000 description 1
- 239000000249 polyoxyethylene sorbitan monopalmitate Substances 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 229920000136 polysorbate Polymers 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 235000019422 polyvinyl alcohol Nutrition 0.000 description 1
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 1
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- ZPWFUIUNWDIYCJ-UHFFFAOYSA-N propan-2-yl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OC(C)C ZPWFUIUNWDIYCJ-UHFFFAOYSA-N 0.000 description 1
- RUOJZAUFBMNUDX-UHFFFAOYSA-N propylene carbonate Chemical compound CC1COC(=O)O1 RUOJZAUFBMNUDX-UHFFFAOYSA-N 0.000 description 1
- 239000003531 protein hydrolysate Substances 0.000 description 1
- 150000004671 saturated fatty acids Chemical class 0.000 description 1
- 235000003441 saturated fatty acids Nutrition 0.000 description 1
- 239000008159 sesame oil Substances 0.000 description 1
- 235000011803 sesame oil Nutrition 0.000 description 1
- 229920002545 silicone oil Polymers 0.000 description 1
- 235000019333 sodium laurylsulphate Nutrition 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000011877 solvent mixture Substances 0.000 description 1
- 235000011076 sorbitan monostearate Nutrition 0.000 description 1
- 239000001587 sorbitan monostearate Substances 0.000 description 1
- 229940035048 sorbitan monostearate Drugs 0.000 description 1
- 239000004544 spot-on Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- OULAJFUGPPVRBK-UHFFFAOYSA-N tetratriacontan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCO OULAJFUGPPVRBK-UHFFFAOYSA-N 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- UFTFJSFQGQCHQW-UHFFFAOYSA-N triformin Chemical compound O=COCC(OC=O)COC=O UFTFJSFQGQCHQW-UHFFFAOYSA-N 0.000 description 1
- 150000004670 unsaturated fatty acids Chemical class 0.000 description 1
- 235000021122 unsaturated fatty acids Nutrition 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
- 210000002268 wool Anatomy 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N53/00—Biocides, pest repellants or attractants, or plant growth regulators containing cyclopropane carboxylic acids or derivatives thereof
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Medicinal Preparation (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Abstract
Description
Die vorliegende Erfindung betrifft ein Verfahren zur Bekämpfung von Ektoparasiten bei Ziegen.The present invention relates to a method for combating of ectoparasites in goats.
Bisher wurde die Ektoparasitenbehandlung bei Ziegen durch Eintauchen (Dippen) oder Besprühen (Sprayen) der ganzen Körperoberfläche des Tieres durchgeführt. Diese Methoden haben jedoch eine Reihe von Nachteilen. Sie beanspruchen relativ viel Zeit, verursachen erhebliche Arbeit und Kosten und stellen für die Tiere einen erheblichen Streß dar. Ferner wurde versucht durch das Aufgießen (Pour-on) von relativ großen Präparatevolumina (meist in Öl formuliert) eine Ektoparasitenbekämpfung bei Ziegen zu erzielen.So far, ectoparasite treatment has been used on goats Immerse (dip) or spray (spray) the whole Body surface of the animal performed. These methods however, have a number of disadvantages. You claim relatively much time, cause considerable work and Cost and cause considerable stress for the animals It was also attempted by pouring on of relatively large specimen volumes (usually formulated in oil) to combat ectoparasites in goats achieve.
Es sind weiterhin Versuche gemacht worden, Ektoparasiten von Ziegen durch enterale oder parenterale Verabreichung von systemisch wirkenden organischen Phosphorverbindungen zu bekämpfen. Attempts have continued to be made to use ectoparasites of goats by enteral or parenteral administration of systemically acting organic phosphorus compounds to fight.
Keine dieser Behandlungsverfahren hatte bisher einen zufriedenstellenden Erfolg, insbesondere gegen Zecken und Milben. Speziell bei der Dip- und Sprayanwendung machte sich die Verschmutzungsgefahr für das Haarkleid, z. B. von Angoraziegen bei der späteren Wollqualität nachteilig bemerkbar.None of these treatments have had one satisfactory success, especially against ticks and Mites. Made especially with the dip and spray application the risk of contamination of the coat, z. B. from Angora goats adversely noticeable in the later wool quality.
Es wurde gefunden, daß man Ektoparasiten bei Ziegen wirkungsvoll bekämpfen kann, indem man sie im Aufgießverfahren mit 0,1-10 ml eines Mittels behandelt, das 2,2- Dimethyl-3-(2,2-dichlorvinyl)-cyclopropan-1-carbonsäure- α-cyano-(3-phenoxy-4-fluor)-benzylester (Cyfluthrin), 2,2-Dimethyl-3-(2,2-dichlorvinyl)-cyclopropan-1- carbonsäurepentafluorbenzylester (Fenfluthrin), 2,2-Dimethyl-3- [2(p-chlorphenyl)-2-chlorvinyl]-cyclopropan-1-carbonsäure- α-cyano-(3-phenoxy-4-fluor)-benzylester (Flumethrin), 2,2-Dimethyl-3-(2,2-dichlorvinyl)-cyclopropan-1- carbonsäure-α-cyano-3-phenoxy-benzylester (Cypermethrin), 2,2-Dimethyl-3-(2,2-dibromvinyl)-cyclopropan-1-carbonsäure- α-cyano-3-phenoxy-benzylester (Deltamethrin) deren Stereoisomere, Enantiomere oder Gemische neben einem oder mehreren hautverträglichen Verdünnungsmitteln, gegebenenfalls in Gegenwart von Emulgatoren und weiteren Hilfsstoffen enthält.It has been found that ectoparasites are found in goats can fight effectively by pouring them on treated with 0.1-10 ml of an agent containing 2.2- Dimethyl-3- (2,2-dichlorovinyl) -cyclopropane-1-carboxylic acid- α-cyano- (3-phenoxy-4-fluoro) benzyl ester (cyfluthrin), 2,2-dimethyl-3- (2,2-dichlorovinyl) cyclopropan-1- pentafluorobenzyl carboxylate (fenfluthrin), 2,2-dimethyl-3- [2 (p-chlorophenyl) -2-chlorovinyl] -cyclopropane-1-carboxylic acid- α-cyano- (3-phenoxy-4-fluoro) benzyl ester (flumethrin), 2,2-dimethyl-3- (2,2-dichlorovinyl) cyclopropan-1- carboxylic acid-α-cyano-3-phenoxy-benzyl ester (cypermethrin), 2,2-dimethyl-3- (2,2-dibromovinyl) -cyclopropane-1-carboxylic acid- α-cyano-3-phenoxy-benzyl ester (deltamethrin) whose Stereoisomers, enantiomers or mixtures in addition to one or several skin-compatible diluents, if necessary in the presence of emulsifiers and other auxiliaries contains.
Mittel dieser Zusammensetzung zeichnen sich vor allem durch ihre schnell einsetzende und sehr lang anhaltende Wirkung aus. Means of this composition stand out above all due to their quick onset and very long lasting Effect out.
Das Aufgießverfahren ist eine an sich bekannte Methode zur Bekämpfung von Ektoparasiten an Rindern (N. M. Rogoff et al J. Econ (1960) S. 814-817). Die dabei eingesetzten Mittel sind als Pour-on- oder Spot-on-Mittel bekannt, wobei die Wirkstoffe meist in größeren Volumina und in Öl formuliert auf den Rücken von Rindern aufgegossen werden. Das Verfahren zeichnet sich durch seine leichte Anwendbarkeit aus. Es konnte jedoch nicht erwartet werden, daß es sich auch zur Bekämpfung von Ektoparasiten bei Ziegen (insbesondere bei Angoraziegen) einsetzen läßt.The pouring process is a known method to control ectoparasites in cattle (N. M. Rogoff et al J. Econ (1960) pp. 814-817). The used Means are known as pour-on or spot-on means, whereby the active ingredients mostly in larger volumes and in oil formulated to be infused on the back of cattle. The process is characterized by its ease of use out. However, it could not be expected to be also to combat ectoparasites in goats (especially with Angora goats).
Von besonderem Vorteil bei der erfindungsgemäßen Methode ist es, daß sehr kleine Volumina der Wirkstoffe oder der entsprechenden wirkstoffhaltigen Formulierungen angewendet werden müssen, um einen Behandlungserfolg zu erzielen. Abhängig von der Größe der zu behandelnden Ziege werden Volumina zwischen 0,1-10 ml (vorzugsweise 1-5 ml) der Formulierung pro Tier angewendet.Of particular advantage in the method according to the invention is it that very small volumes of the active ingredients or the appropriate formulations containing active ingredient applied need to be successful in order to be successful. Dependent on the size of the goat to be treated Volumes between 0.1-10 ml (preferably 1-5 ml) of Formulation applied per animal.
Abhängig von dem jeweiligen Wirkstoff enthält die Formulierung den Wirkstoff in einer 0,01% bis 50% Lösung vorzugsweise in einer 0,1-10% Lösung. Der Wirkstoff wird den Ziegen in einer Menge von 0,01 mg-500 mg pro Tier je nach Wirkstoff verabreicht. Die Formulierung kann sowohl bei langhaarigen als auch bei geschorenen Ziegen verabreicht werden.Depending on the active ingredient, the formulation contains the active ingredient in a 0.01% to 50% solution is preferred in a 0.1-10% solution. The active ingredient will the goats in an amount of 0.01 mg-500 mg per animal administered depending on the active ingredient. The wording can both long-haired and shorn goats be administered.
Als Ektoparasiten der Ziegen, die mit den erfindungsgemäßen Formulierungen und den genannten Wirkstoffen bekämpft werden können seien beispielsweise genannt. As ectoparasites of goats, which with the invention Formulations and the active ingredients mentioned can be mentioned for example.
Hypoderma aeratum, Hypoderma crossi, Damalinia caprae, Bovicola painei, Damalinla limbata, Linognathus stenopsis, Otobius megnini, Ixodes pilosus, Ixodes rubicundus, Boophilus decoloratus, Hyalomma aegyptium, Rhipicephalus appendiculatus, Rhipicephalus evertsi, Amblyomma hebraeum, Amblyomma variegatum, Sarcoptes scabiei, Psoroptes communis caprae, Demodex caprae.Hypoderma aeratum, Hypoderma crossi, Damalinia caprae, Bovicola painei, Damalinla limbata, Linognathus stenopsis, Otobius magnini, Ixodes pilosus, Ixodes rubicundus, Boophilus decoloratus, Hyalomma aegyptium, Rhipicephalus appendiculatus, Rhipicephalus evertsi, Amblyomma hebraeum, Amblyomma variegatum, Sarcoptes scabiei, Psoroptes communis caprae, Demodex caprae.
Die Mittel werden in an sich bekannter Weise hergestellt indem der Wirkstoff oder Mischungen der Wirkstoffe in einem oder mehreren hautverträglichen Verdünnungsmitteln gelöst oder suspendiert und gegebenenfalls weitere Hilfsstoffe zugesetzt werden.The agents are produced in a manner known per se by the active ingredient or mixtures of the active ingredients in one or more skin-compatible diluents dissolved or suspended and optionally others Auxiliaries are added.
Geeignete Verdünnungsmittel sind Alkohole, wie Ethylalkohol, Isopropylalkohole, n-Butylalkohol, Amylalkohol, Octanol.Suitable diluents are alcohols, such as ethyl alcohol, Isopropyl alcohols, n-butyl alcohol, amyl alcohol, Octanol.
Glykole, wie Propylenglykol, 1,3-Butylenglykol, Ethylglykol, Dipropylenglykolmonomethylether.Glycols, such as propylene glycol, 1,3-butylene glycol, ethyl glycol, Dipropylene glycol monomethyl ether.
Aromatische Alkohole wie Benzylalkohol.Aromatic alcohols such as benzyl alcohol.
Carbonsäureester, wie z. B. Ethylacetat, Benzylbenzoat, Butylacetat, Propylencarbonat, Milchsäureethylester.Carboxylic acid esters, such as. B. ethyl acetate, benzyl benzoate, Butyl acetate, propylene carbonate, lactic acid ethyl ester.
Aliphatische Kohlenwasserstoffe, Öle, die nicht unter die Definition der spreitenden Öle fallen, wie z. B. Baumwollsaatöl, Erdnußöl, Maiskernöl, Olivenöl, Ricinusöl, Sesamöl. Aliphatic hydrocarbons, oils that are not under the definition of spreading oils fall, such as B. Cottonseed oil, peanut oil, corn kernel oil, olive oil, Castor oil, sesame oil.
Ketone, wie z. B. Aceton und Methylethylketon.Ketones such as B. acetone and methyl ethyl ketone.
Synth. Mono- und Triglyceride mit natürlichen Fettsäuren.Synth. Mono- and triglycerides with natural fatty acids.
Weiterhin sind u. a. Verbindungen wie Dimethylsulfoxid, Dimethylacetamid, Dimethylformamid, N-Methylpyrolidon, Dioxan, 2-Dimethyl-4-oxymethyl-1,3-dioxalan gut als Verdünnungsmittel geeignet.Furthermore, a. Compounds such as dimethyl sulfoxide, Dimethylacetamide, dimethylformamide, N-methylpyrolidone, Dioxane, 2-dimethyl-4-oxymethyl-1,3-dioxalane works well as Suitable diluent.
Besonders gut geeignet sind niedere Alkohole mit bis zu 8 Kohlenstoffatomen im Molekül, sowie niedere Ketone wie Methylethylketon und Ether des Ethylenglykols und des Propylenglykols.Lower alcohols with up to 8 carbon atoms are particularly suitable in the molecule, as well as lower ketones such as Methyl ethyl ketone and ether of ethylene glycol and Propylene glycol.
Es können bei der Herstellung der erfindungsgemäß verwendbaren Mittel ein oder mehrere Verdünnungsmittel eingesetzt werden.It can be used in the production of the usable according to the invention Means one or more diluents be used.
Als weitere Hilfsstoffe sind geeignet:
a)Haftvermittler, z. B. Carboxmethylcellulose, Methylcellulose
und andere Celllose- und Stärke-Derivate,
Polyacrylate, Alginate, Gelatine, Gummiarabicum
Polyvinylpyrrolidon, Polyvinylalkohol, Copolymere
aus Methylvinylether und Maleinsäureanhydrid, Polyethylenglykole,
Paraffine, Öle, Wachse, hydriertes
Rizinusöl.
Kolloidale Kieselsäure oder Gemische der aufgeführten
Stoffe. Lösungen und Emulgatoren können
neben dem Wirkstoff die üblichen Trägerstoffe enthalten,
wie
b) Tenside (beinhaltet Emulgatoren und Netzmittel),
z. B.
1. anionaktive, wie Na-Laurylsulfat, Fettalkoholethersulfate,
Mono/Dialkylpolyglykoletherorthophosphorsäureester-
Monoethanolaminsalz,
Calciumalkylarylsulfonat,
2. kationaktive, wie Cethyltrimethylammoniumchlorid,
3. ampholytische, wie Di-Na-N-lauryl-:-iminodipropionat
oder Lecithin,
4. nicht ionogene, z. B. polyoxyethyliertes
Ricinusöl, polyoxyethyliertes Sorbitan-Monooleat,
Sorbitan-Monostearat, Glycerinmonostearat,
Polyoxyethylenstearat, Alkylphenolpolyglykolether.
c) Spreitmittel wie z. B.
Silikonöle verschiedener Viskosität
Fettsäureester wie Ethylstearat, Di-n-butyl-adipat,
Laurinsäurehexylester, Dipropylen-glykolpelargonat,
Ester einer verzweigten Fettsäure mittlerer Kettenlänge
mit gesättigten Fettalkoholen C16-C18, Isopropylmyristat,
Isopropylpalmitat, Capryl/Caprinsäureester
von gesättigten Fettalkoholen der
Kettenlänge C12-C18, Isopropylstearat, Ölsäureoleylester,
Ölsäuredecylester, Ethyloleat, Milchsäureethylester,
wachsartige Fettsäureester wie
künstliches Entenbürzeldrüsenfett, Dibutylphthalat,
Adipinsäurediisopropylester, letzterem verwandte
Estergemische u. a.
Triglyceride wie Capryl/Caprinsäuretriglycerid,
Triglyceridgemische mit Pflanzenfettsäuren der
Kettenlänge C8-C12 oder anderen speziell ausgewählten
natürlichen Fettsäuren, Partialglyceridgemische
gesättigter oder ungesättigter evtl. auch
hydroxylgruppenhaltige Fettsäuren, Monodiglyceride
der C8/C10-Fettsäuren und andere.
Fettalkohole wie Isotridecylalkohol, 2-Octyldodecanol,
Cetylstearylalkohol, Oleylalkohol.
Fettsäuren wie z. B. Ölsäure.
Besonders gut geeignete spreitende Öle sind die
folgenden:
Isopropylmyristat, Isopropylpalmitat, Capryl/Caprinsäureester
von gesättigten Fettalkoholen der
Kettenlänge C12-C18, wachsartige Fettsäureester wie
künstliches Entenbürzeldrüsenfett.The following are also suitable as auxiliary substances:
a) adhesion promoter, e.g. B. carboxmethyl cellulose, methyl cellulose and other cellulose and starch derivatives, polyacrylates, alginates, gelatin, gum arabic, polyvinyl pyrrolidone, polyvinyl alcohol, copolymers of methyl vinyl ether and maleic anhydride, polyethylene glycols, paraffins, oils, waxes, hydrogenated castor oil.
Colloidal silica or mixtures of the listed substances. In addition to the active ingredient, solutions and emulsifiers can contain the usual carriers, such as
b) surfactants (contains emulsifiers and wetting agents), e.g. B.
1. anionic, such as sodium lauryl sulfate, fatty alcohol ether sulfates, mono / dialkyl polyglycol ether orthophosphoric acid ester monoethanolamine salt, calcium alkylarylsulfonate,
2. cationic, such as methyl trimethyl ammonium chloride,
3. ampholytic, such as di-Na-N-lauryl: iminodipropionate or lecithin,
4. non-ionogenic, e.g. B. polyoxyethylated castor oil, polyoxyethylated sorbitan monooleate, sorbitan monostearate, glycerol monostearate, polyoxyethylene stearate, alkylphenol polyglycol ether.
c) spreading agents such. B.
Silicone oils of different viscosities
Fatty acid esters such as ethyl stearate, di-n-butyl adipate, lauric acid hexyl ester, dipropylene glycol pelargonate, esters of a branched fatty acid of medium chain length with saturated fatty alcohols C 16 -C 18 , isopropyl myristate, isopropyl palmitate, caprylic / capric acid esters of saturated fatty alcohols 18 of chain length C 12 , Isopropyl stearate, oleic acid oleyl ester, oleic acid decyl ester, ethyl oleate, lactic acid ethyl ester, waxy fatty acid esters such as artificial duckling gland fat, dibutyl phthalate, adipic acid diisopropyl ester, the latter related ester mixtures and others
Triglycerides such as caprylic / capric acid triglyceride, triglyceride mixtures with vegetable fatty acids of chain length C 8 -C 12 or other specially selected natural fatty acids, partial glyceride mixtures of saturated or unsaturated fatty acids, which may also contain hydroxyl groups, monodiglycerides of C 8 / C 10 fatty acids and others.
Fatty alcohols such as isotridecyl alcohol, 2-octyldodecanol, cetylstearyl alcohol, oleyl alcohol.
Fatty acids such as B. oleic acid.
The following are particularly suitable spreading oils:
Isopropyl myristate, isopropyl palmitate, caprylic / capric acid esters of saturated fatty alcohols with chain length C 12 -C 18 , wax-like fatty acid esters such as artificial duckling glandular fat.
Als Mittel für das erfindungsgemäße Verfahren kommen jedoch auch übliche Suspensions- und Emulsionskonzentrate in Frage, die vor Gebrauch mit Wasser auf die gewünschte Anwendungskonzentrate verdünnt werden. However, as a means for the process according to the invention also conventional suspension and emulsion concentrates in question, before using water to the desired one Application concentrates are diluted.
Diese Formulierungen werden in bekannter Weise hergestellt, z. B. durch Vermischen des Wirkstoffs mit Streckmitteln, also flüssigen Lösungsmitteln, gegebenenfalls unter Verwendung von oberflächenaktiven Mitteln, also Emulgiermitteln und/oder Dispergiermitteln und/oder schaumerzeugenden Mitteln. Im Falle der Benutzung von Wasser als Streckmittel können z. B. auch organische Lösungsmittel als Hilfslösungsmittel verwendet werden. Als flüssige Lösungsmittel kommen im wesentlichen in Frage: Aromaten, wie Xylol, Toluol, oder Alkylnaphthaline, chlorierte Aromaten oder chlorierte aliphatische Kohlenwasserstoffe, wie Chlorbenzole, Chlorethylene oder Methylenchlorid, aliphatische Kohlenwasserstoffe, wie Cyclohexan oder Paraffine, z. B. Erdölfraktionen, Alkohole, wie Butanol oder Glykol sowie deren Ether und Ester, Ketone, wie Aceton, Methylethylketon, Methylisobutylketon oder Cyclohexanon, stark polare Lösungsmittel, wie Dimethylformamid und Dimethylsulfoxid, sowie Wasser: als Emulgier- und/oder schaumerzeugende Mittel kommen in Frage: z. B. nichtionogene und anionische Emulgatoren, wie Polyoxyethylen-Fettsäure-Ester, Polyoxyethylen-Fettalkohol- Ether, z. B. Alkylarylpolyglykol-Ether, Alkylsulfonate, Alkylsulfate, Arylsulfonate sowie Eiweißhydrolysate; als Dispergiermittel kommen in Frage: z. B. Lignin-Sulfitablaugen und Methylcellulose.These formulations are prepared in a known manner e.g. B. by mixing the active ingredient with Extenders, that is liquid solvents, if appropriate using surfactants, thus emulsifiers and / or dispersants and / or foaming agents. In case of using Water as an extender can e.g. B. also organic solvents can be used as auxiliary solvents. As Liquid solvents are essentially: Aromatics, such as xylene, toluene, or alkylnaphthalenes, chlorinated aromatics or chlorinated aliphatic Hydrocarbons such as chlorobenzenes, chlorethylenes or Methylene chloride, aliphatic hydrocarbons, such as Cyclohexane or paraffins, e.g. B. petroleum fractions, alcohols, such as butanol or glycol and their ethers and esters, Ketones such as acetone, methyl ethyl ketone, methyl isobutyl ketone or cyclohexanone, strongly polar solvents, such as Dimethylformamide and dimethyl sulfoxide, as well as water: as Emulsifying and / or foaming agents come in Question: e.g. B. nonionic and anionic emulsifiers, such as Polyoxyethylene fatty acid esters, polyoxyethylene fatty alcohol Ethers, e.g. B. alkylaryl polyglycol ethers, alkyl sulfonates, Alkyl sulfates, aryl sulfonates and protein hydrolyzates; as Dispersants come into question: z. B. Lignin sulfite liquor and methyl cellulose.
Es können in den Formulierungen Haftmittel wie Carboxymethylcellulose, natürliche und synthetische pulverige, körnige oder latexförmige Polymere verwendet werden, wie Gummiarabicum, Polyvinylalkohol, Polyvinylacetat, sowie natürliche Phospholipide, wie Kephaline und Lecithine, und synthetische Phospholipide. Weitere Additive können mineralische und vegetabile Öle sein.In the formulations, adhesives such as carboxymethyl cellulose, natural and synthetic powdery, granular or latex-shaped polymers can be used, such as Gum arabic, polyvinyl alcohol, polyvinyl acetate, as well natural phospholipids, such as cephalins and lecithins, and synthetic phospholipids. Other additives can mineral and vegetable oils.
Es können Farbstoffe wie anorganische Pigmente, z. B. Eisenoxid, Titanoxid, Ferrocyanblau und organische Farbstoffe, wie Alizarin-, Azo- und Metallphthalocyaninfarbstoffe enthalten sein.Dyes such as inorganic pigments, e.g. B. Iron oxide, titanium oxide, ferrocyan blue and organic Dyes such as alizarin, azo and metal phthalocyanine dyes be included.
Als Mittel für das erfindungsgemäße Verfahren kommen auch wasserhaltige Mikroemulsionen in Frage. Solche enthalten 0,1-10% Wirkstoff, 1-30% eines oberflächenaktiven Mittels, gegebenenfalls 20-70% eines mit Wasser mischbaren Verdünnungsmittels sowie gegebenenfalls 0-5% Hilfsmittel, wobei der Rest aus Wasser besteht.Also come as means for the method according to the invention water-containing microemulsions in question. Such contain 0.1-10% active ingredient, 1-30% of a surfactant By means of, optionally 20-70% of a water-miscible Diluent and optionally 0-5% Tools, the rest of which consists of water.
Als oberflächenaktive Mittel seien genannt: nicht-ionische, wasserlösliche Emulgatoren mit einem HLB (hydrophilic/lipophilic/balance-Wert) größer als 10, z. B. W® (Bayer AG), Alkylarylpolyglykolether, Emulgator NP 10® (Bayer AG), Alkylarylpolyglykolether; Renex 678® (Atlas Chemical Industries), Polyoxyethylenalkylarylether; Tween 40® (Atlas), Polyoxyethylensorbitanmonopalmitat; Myri 53® (Atlas), Polyoxyethylenstearat; Atlas G 3707®, Polyoxyethylenlaurylether; Atlas G 3920®, Polyoxyethylene oleylether; Atlas G 9046 T®, Polyoxyethylenmannitanmonolaurat; Emulgator 1371 B® (Bayer AG), Alkylpolyglykolether; Emulgator 1736® (Bayer AG), Alkylpolyglykolether (Oleylpolyglykolether); Emulgator OX® (Bayer AG), Alkylpolyglykolether (Dodecylpolyglykolether); Ninox BM-2® (Stephan Chemical Co.), ethoxyliertes Nonylphenol; Triton X-100® (Rohm an Haas Co.), Isooctylphenolpolyethoxyethanol; Cremophor EL®.The following may be mentioned as surface-active agents: non-ionic, water-soluble emulsifiers with an HLB (hydrophilic / lipophilic / balance value) greater than 10, e.g. B. W® (Bayer AG), alkylaryl polyglycol ether, emulsifier NP 10® (Bayer AG), alkylaryl polyglycol ether; Renex 678® (Atlas Chemical Industries), polyoxyethylene alkyl aryl ether; Tween 40® (Atlas), polyoxyethylene sorbitan monopalmitate; Myri 53® (Atlas), polyoxyethylene stearate; Atlas G 3707®, polyoxyethylene lauryl ether; Atlas G 3920®, polyoxyethylene oleyl ether; Atlas G 9046 T®, Polyoxyethylene mannitan monolaurate; Emulsifier 1371 B® (Bayer AG), alkyl polyglycol ether; Emulsifier 1736® (Bayer AG), alkyl polyglycol ether (oleyl polyglycol ether); Emulsifier OX® (Bayer AG), alkyl polyglycol ether (dodecyl polyglycol ether); Ninox BM-2® (Stephan Chemical Co.), ethoxylated nonylphenol; Triton X-100® (Rohm an Haas Co.), Isooctylphenol polyethoxyethanol; Cremophor EL®.
Als Lösungsmittel seien genannt: Methanol, Ethanol, Propanol, vorzugsweise Isopropanol, Dimethylsulfoxid, Dimethylsulfoxid, Dimethylformamid, Glycerine, Ethylenglykolmonomethylether, Diethylglykolmonomethylether (Methoxyethoxyethanol, Methyl carbitol), Polyethylenglykole, Propylenglykole, Polypropylenglykole sowie Ketone wie Aceton und Methylethylketon.The following may be mentioned as solvents: methanol, ethanol, Propanol, preferably isopropanol, dimethyl sulfoxide, Dimethyl sulfoxide, dimethylformamide, glycerols, ethylene glycol monomethyl ether, Diethyl glycol monomethyl ether (Methoxyethoxyethanol, methyl carbitol), polyethylene glycols, Propylene glycols, polypropylene glycols as well Ketones such as acetone and methyl ethyl ketone.
Die Mittel werden hergestellt durch Lösen des oder der Wirkstoffe in einem Emulgator oder in einem Emulgator- Lösungsmittelgemisch unter Erwärmung, falls notwendig, und durch Zugabe des erforderlichen Anteils Wasser unter Rühren. Eine besondere Homogenisierungsvorrichtung ist nicht erforderlich.The agents are made by loosening the or the Active ingredients in an emulsifier or in an emulsifier Solvent mixture with heating, if necessary and by adding the required amount of water under Stir. A special homogenizer is not mandatory.
Besonders bevorzugt werden die in DE-OS 32 08 334 beschriebenen Formulierungen eingesetzt. Herstellung und Zusammensetzung dieser Formulierungen kann im einzelnen der DE-OS 32 08 334 entnommen werden.Those described in DE-OS 32 08 334 are particularly preferred Formulations used. Manufacture and The composition of these formulations may vary can be taken from DE-OS 32 08 334.
Claims (2)
Priority Applications (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19853531920 DE3531920A1 (en) | 1985-09-07 | 1985-09-07 | Method for combating ectoparasites in goats |
| ZA866752A ZA866752B (en) | 1985-09-07 | 1986-09-05 | Method for combating ectoparasites of goats |
| AU62428/86A AU6242886A (en) | 1985-09-07 | 1986-09-08 | Method for combating ectoparasites of goats by fluthrin and methrin derivatives |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19853531920 DE3531920A1 (en) | 1985-09-07 | 1985-09-07 | Method for combating ectoparasites in goats |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE3531920A1 true DE3531920A1 (en) | 1987-03-12 |
Family
ID=6280329
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE19853531920 Withdrawn DE3531920A1 (en) | 1985-09-07 | 1985-09-07 | Method for combating ectoparasites in goats |
Country Status (3)
| Country | Link |
|---|---|
| AU (1) | AU6242886A (en) |
| DE (1) | DE3531920A1 (en) |
| ZA (1) | ZA866752B (en) |
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2001040446A1 (en) * | 1999-12-02 | 2001-06-07 | Lilly Co Eli | Pour-on formulations |
| WO2002050042A3 (en) * | 2000-12-21 | 2002-11-28 | Bayer Ag | Use of pyrazol oximes as parasiticidal agents |
| DE10337305A1 (en) * | 2003-07-02 | 2005-02-03 | Andresen, Uwe, Prof. Dr. | Parasiticides, repellant composition and process for their preparation and use |
| US7772194B2 (en) | 2001-09-17 | 2010-08-10 | Eli Lilly And Company | Pesticidal formulations |
| WO2011103694A1 (en) | 2010-02-26 | 2011-09-01 | Solnova Ag | Spot-on preparation with parasite-repelling action |
| DE202012004045U1 (en) | 2012-04-16 | 2012-05-02 | Solnova Ag | Spot-on preparation |
| EP3771335A1 (en) | 2019-07-31 | 2021-02-03 | Athenion AG | Repellent composition |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU620863B2 (en) * | 1989-04-21 | 1992-02-27 | Sentrachem Limited | Liquid pour-on formulation |
-
1985
- 1985-09-07 DE DE19853531920 patent/DE3531920A1/en not_active Withdrawn
-
1986
- 1986-09-05 ZA ZA866752A patent/ZA866752B/en unknown
- 1986-09-08 AU AU62428/86A patent/AU6242886A/en not_active Abandoned
Cited By (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2001040446A1 (en) * | 1999-12-02 | 2001-06-07 | Lilly Co Eli | Pour-on formulations |
| WO2001040446A3 (en) * | 1999-12-02 | 2002-01-17 | Lilly Co Eli | Pour-on formulations |
| US6955818B1 (en) | 1999-12-02 | 2005-10-18 | Eli Lilly And Company | Pour-on formulations |
| WO2002050042A3 (en) * | 2000-12-21 | 2002-11-28 | Bayer Ag | Use of pyrazol oximes as parasiticidal agents |
| US7772194B2 (en) | 2001-09-17 | 2010-08-10 | Eli Lilly And Company | Pesticidal formulations |
| US8048861B2 (en) | 2001-09-17 | 2011-11-01 | Eli Lilly And Company | Pesticidal formulations |
| DE10337305A1 (en) * | 2003-07-02 | 2005-02-03 | Andresen, Uwe, Prof. Dr. | Parasiticides, repellant composition and process for their preparation and use |
| WO2011103694A1 (en) | 2010-02-26 | 2011-09-01 | Solnova Ag | Spot-on preparation with parasite-repelling action |
| DE202012004045U1 (en) | 2012-04-16 | 2012-05-02 | Solnova Ag | Spot-on preparation |
| EP2653034A1 (en) | 2012-04-16 | 2013-10-23 | Solnova AG | Spot-on preparation with parasite-repelling action for topical application to animals |
| EP3771335A1 (en) | 2019-07-31 | 2021-02-03 | Athenion AG | Repellent composition |
| EP3771336A1 (en) | 2019-07-31 | 2021-02-03 | Athenion AG | Repellent composition |
Also Published As
| Publication number | Publication date |
|---|---|
| ZA866752B (en) | 1987-05-27 |
| AU6242886A (en) | 1987-03-12 |
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