FI122765B - Insekticidkomposition för däggdjurs, i synnerhet för hundars och katters loppor - Google Patents
Insekticidkomposition för däggdjurs, i synnerhet för hundars och katters loppor Download PDFInfo
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- FI122765B FI122765B FI20115199A FI20115199A FI122765B FI 122765 B FI122765 B FI 122765B FI 20115199 A FI20115199 A FI 20115199A FI 20115199 A FI20115199 A FI 20115199A FI 122765 B FI122765 B FI 122765B
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- YHAIUSTWZPMYGG-UHFFFAOYSA-L disodium;2,2-dioctyl-3-sulfobutanedioate Chemical compound [Na+].[Na+].CCCCCCCCC(C([O-])=O)(C(C([O-])=O)S(O)(=O)=O)CCCCCCCC YHAIUSTWZPMYGG-UHFFFAOYSA-L 0.000 description 1
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- 125000003438 dodecyl group Chemical class [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
- 244000079386 endoparasite Species 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
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- 229930195729 fatty acid Natural products 0.000 description 1
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- 235000011187 glycerol Nutrition 0.000 description 1
- RGNPBRKPHBKNKX-UHFFFAOYSA-N hexaflumuron Chemical compound C1=C(Cl)C(OC(F)(F)C(F)F)=C(Cl)C=C1NC(=O)NC(=O)C1=C(F)C=CC=C1F RGNPBRKPHBKNKX-UHFFFAOYSA-N 0.000 description 1
- 230000003054 hormonal effect Effects 0.000 description 1
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- YWTYJOPNNQFBPC-UHFFFAOYSA-N imidacloprid Chemical compound [O-][N+](=O)\N=C1/NCCN1CC1=CC=C(Cl)N=C1 YWTYJOPNNQFBPC-UHFFFAOYSA-N 0.000 description 1
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- 229940067606 lecithin Drugs 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- 239000000594 mannitol Substances 0.000 description 1
- 235000010355 mannitol Nutrition 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
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- 150000004180 methoprene derivatives Chemical class 0.000 description 1
- 230000003278 mimic effect Effects 0.000 description 1
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- ZHALDANPYXAMJF-UHFFFAOYSA-N octadecanoate;tris(2-hydroxyethyl)azanium Chemical compound OCC[NH+](CCO)CCO.CCCCCCCCCCCCCCCCCC([O-])=O ZHALDANPYXAMJF-UHFFFAOYSA-N 0.000 description 1
- 239000002674 ointment Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 125000000913 palmityl 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])([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
- 230000000803 paradoxical effect Effects 0.000 description 1
- 230000001717 pathogenic effect Effects 0.000 description 1
- 239000000546 pharmaceutical excipient Substances 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 239000000473 propyl gallate Substances 0.000 description 1
- 235000010388 propyl gallate Nutrition 0.000 description 1
- 229940075579 propyl gallate Drugs 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- NHDHVHZZCFYRSB-UHFFFAOYSA-N pyriproxyfen Chemical compound C=1C=CC=NC=1OC(C)COC(C=C1)=CC=C1OC1=CC=CC=C1 NHDHVHZZCFYRSB-UHFFFAOYSA-N 0.000 description 1
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 1
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- 229910052708 sodium Inorganic materials 0.000 description 1
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- 235000013616 tea Nutrition 0.000 description 1
- 229940029614 triethanolamine stearate Drugs 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
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Classifications
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- A—HUMAN NECESSITIES
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- 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
- A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
- A01N25/02—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests containing liquids as carriers, diluents or solvents
-
- 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
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/56—1,2-Diazoles; Hydrogenated 1,2-diazoles
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- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/12—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing the group, wherein Cn means a carbon skeleton not containing a ring; Thio analogues thereof
-
- 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
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
- A01N43/40—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom six-membered rings
-
- 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
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/02—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having no bond to a nitrogen atom
-
- 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
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/28—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N<
- A01N47/34—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N< containing the groups, e.g. biuret; Thio analogues thereof; Urea-aldehyde condensation products
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/49—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds
- A61K8/494—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with more than one nitrogen as the only hetero atom
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/0012—Galenical forms characterised by the site of application
- A61K9/0014—Skin, i.e. galenical aspects of topical compositions
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- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P33/00—Antiparasitic agents
- A61P33/14—Ectoparasiticides, e.g. scabicides
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q17/00—Barrier preparations; Preparations brought into direct contact with the skin for affording protection against external influences, e.g. sunlight, X-rays or other harmful rays, corrosive materials, bacteria or insect stings
- A61Q17/02—Barrier preparations; Preparations brought into direct contact with the skin for affording protection against external influences, e.g. sunlight, X-rays or other harmful rays, corrosive materials, bacteria or insect stings containing insect repellants
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Agronomy & Crop Science (AREA)
- Engineering & Computer Science (AREA)
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- Zoology (AREA)
- Environmental Sciences (AREA)
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- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- Dermatology (AREA)
- Epidemiology (AREA)
- Medicinal Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Toxicology (AREA)
- Birds (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Tropical Medicine & Parasitology (AREA)
- Organic Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Medicinal Preparation (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Claims (37)
1. Användning av ä ena sidan förening (A) med formeS 1-[2,6-Ci2~4-CF3-fenyi]-2-CN-4-[SO-CF3]-5-NH2-pyrazol och a and ra sidan minst en ovicid förening (B), som är av typen IGR (ett ämne som regierar insekters tiiiväxt), i 5 en vätskeformig vehikel, som är godtagber för djur och lämplig för loka! ”spot-on”-appiicering pä huden, för framställning av en komposition, som är avsedd att administreras lokalt punkt för punkt via huden som ett längvarigt skydd mot ioppor och fäs-tingar hos smä daggdjur, främst hundar och katter, 10 varvid den vätskeformiga bäraren och föreningarnas (A) och (B) hait anordnas sä att den appliceras punkt för punkt "pour-on"-typiskt pä huden och i komposition förening (A) är närvarande i mängd av 1 - 20 % (w/v) och förening (B) är närvarande i mängd av 1 - 20 % (w/v).
2. Användning enligt patentkrav 1, kä n neteckn ad av att minst en förening (B), som är av IGR-typ och som sparar ungdomshormoner.
3. Användning enligt patentkrav 1, kännetecknad av att minst en förening (B), som är av IGR-typ är inhibitor av syntesen av kitin.
4. Användning enligt patentkrav 1, k ä n n e t e c k n a d av att en 20 förening (B) som sparar ungdomshormoner, väljs frän gruppen: azadiraktin, diofenolan, fenoxikarb, hydropren, kinopren, metopren, pyriproxifen, tetrahyd-roazadiraktin, och 4-k!or-2-(2-kIor-2-metylpropyl)-5-(6-jod-3-pyr!dylmetoxi)pyri-dizin-3(2H)-on.
5. Användning enligt patentkrav 3, k ä n n e t e c k n a d av att inhi-25 bitor av syntesen av kitin väljs frän guppen som bestär av klorfluazuron, cyro- ^ mazin, diflubensuron, fluazuron, flucykloxuron, flufenoxuron, gexaflumuron, lu- O ^ fenuron, ebufenozid, teflubensuron, triflumuron, 1-(2,6-difluorbensoyl)-3-(2- o fluor-4-(trifluorrnetyl)fenylurea, 1-(2,6-dif!uorbensoyl)-3-(2-fluor-4-(1,1,2,2-tetra- g fluoretoxl)fenyiurea, och 1-(2,6-difluorbensoyl)-3-(2-fluor-4-trifluormetyi)fenyl- g 30 urea. CL
8. Användning enligt patentkrav 4, kännetecknad av att en O) förening (B) som sparar ungdomshormoner, väljs frän gruppen: diofenolan, ^ metopren, pyriproxifen, hydropren. oj 7. Användning enligt patentkrav 4, kännetecknad av att en 35 förening (B) som sparar ungdomshormoner är pyriproxifen.
8, Användning enligt patentkrav 4, k ä n n e t e c k n a d av att en förening (B) som spärar ungdomshormoner är metopren.
9. Användning enligt patentkrav 4, k ä n n e t e c k n a d av att en förening (B) som spärar ungdomshormoner är diofenolan.
10. Användning enligt patentkrav 4, k ä n n e t e c k n a d av att en förening (B) som spärar ungdomshormoner är fenoxikarb.
11. Användning enligt nägot av patentkraven 1-10, känne-t e c k n a d av att viktförhäilandet för föreningarna (A) enligt forme! (I) och för-eningarna av typ (B) är 80:20 - 20:80,
12. Användning enligt nägot av patentkraven 1-11, känne- t e c k n a d av att den vätskeformiga bäraren och föreningarnas (A) och (B) hait anordnas för lokal administrering pä ett omräde, vars yta är under 10 cm2.
13. Användning enligt patentkrav 12, kännetecknad av att den vätskeformiga bäraren och föreningarnas (A) och (B) hait anordnas för Ιοί 5 kai administrering pä tvä ställen vilka företrädesvis är belägna mellan djurens skuldror.
14. Användning enligt nägot av patentkraven 1-13, känne-t e c k n a d av att den omfattar en dos 0,1 - 40 mg/kg av förening (A) och en dos 0.1 - 40 mg/kg av förening (B).
15. Användning enligt patentkrav 14, kännetecknad av att den omfattar en dos 1 - 20 mg/kg av förening (A) och en dos 1-30 mg/kg av förening (B).
18. Användning eniigt nägot av patentkraven 1-15, kännetecknad av att den dessutom omfattar en kristalliseringsinhibitor (b).
17. Användning enligt patentkrav 16, kännetecknad av att kristalliseringsinhibitor (b) är närvarande företrädesvis i en mängd av 1 - 20 % (M 5 (vv/v). ^ 18. Användning enligt patentkrav 16 eller 17, kännetecknad 9 av att kristalliseringsinhibitom (b) väljs frän gruppen som bestär av följande: CO o 30 poiyvtnylpyrrolidon, polyvinylalkohoier, vinylacetat och kopolymerer c av vinylpyrrolidon, polyetylenglykoler, bensylalkoho!, mannitol, glycerol, sorbien toi, estrar av sorbitanpolyoxietylener; lecitin, natriumkarboximetylcellulosa, ^ akrylderivat säsom metakrylater och motsvarande, ^ anjoniska ytaktiva ämnen, säsom alkali-, främst natrium-, kalium- el- ^ 35 ler ammonium-, stearater; kalciumstearat; trietanolaminstearat; natriumabietat; aikylsulfater, främst natriumiaurylsuifat och natriumsetyisulfat; natriumdodekyl-bensensulfonai, natriumdioktyisuifosuckinat; fettsyror, främst kopraoljederivat, katjoniska ytaktiva ämnen säsom vattenlösliga kvaternära ammoni-umsalter med forme! N+R‘R,,R,,‘R""Y'I väri radikalerna R är kolväteradikaler, 5 som eventueilt är hydroxylerade, och Y" är en stark syras anjon, säsom nägon halogenid-, sulfat- och sulfonatanjon; setyltrimetyiammoniumbromid räknas tii! de användbara katjoniska ytaktiva ämnena, aminsalter med forme! N+R'R"R’", där radikaierna R är kolväteradikaler, som eventueilt är hydroxylerade; oktadecySaminhydroklorid räknas tili de 10 användbara katjoniska ytaktiva ämnena, icke-joniska ytaktiva ämnen säsom sorbitanestrar, som eventueilt är polyoxietylenerade, särskilt preparat Polysorbate 80, polyoxietynelerade al-kyletrar; polyetyienglykolstearat, ricinoljas polyoxietylenerade derivat, polygly-cerolestrar, polyoxietylenerade fettalkoholer, polyoxietylenerade fettsyror, ety-15 lenoxid och kopolymerer av propylenoxid, amfotera ytaktiva ämnen säsom substituerade laurylderivat av detain, eller företrädesvis en blandning av minst tvä nämnda.
19, Användning enligt patentkrav 18, kännetecknad avatt 20 katjoniska ytaktiva ämne är setyltrimetyiammoniumbromid.
20, Användning enligt patentkrav 18, kän netecknad av att aminsalt är oktadecylaminhydroklorid.
21, Användning enligt nägot av patentkraven 16 - 20, kännetecknad av att den omfattar ett kristailiseringsinhibitorpar, som har bildats 25 genom att förena ett filmogent ämne av poiymertyp och ett ytaktivt ämne, företrädesvis i mängder, som är närä kristalliseringsinhibitorns totalmängders C\J £ gräns eller identiska i förhallande tili den. ^ 22. Användning enligt patentkrav 21, kännetecknad av att 9 filmogena ämnet väljs frän gruppen som bestär av följande: CO o 30 polyvinylpyrrolidone olika kvaliteter, ir polyvinyialkoholer och ^ kopolymerer av vinylacetat och vinylpyrrolidon, 2 och att det ytaktiva ämnet väljs fran icke-joniska aktiva ämnen. ^ 23. Användning enligt patentkrav 22, kännetecknad av att o ^ 35 icke-joniskt aktivt ämne är polyoxietynelerade sorbitanester.
24. Användning enligt patentkrav 23, k ä n n e t e c k n a d av att po iyoxietyneierade sorbitanester är polysorbate,
25. Användning enligt nagot av patentkraven 1-24, känne-t e c k n a d av att den omfattar ett organiskt iösningsmedei (c), vars dielektrici- 5 tetskonstant är 10-35, varvid halien av detta Iösningsmedei I totalkomposit-ionen motsvarar företrädesvis en 100 % kompositions komplement.
26. Användning enligt patentkrav 25, k ä n n e t e c k n a d av att det organiska lösningsmedlet (c) väljs frän följande: aceton, acetonitril, bensyialko-hol, butyldiglykol, dimetyiacetamid, dimetylformamid, dipropylenglykols n-bu- 10 tyleter, etanol, isopropanoi, metanol, etylenglykols monoetyieter, etylenglykols monometyleter, monometylacetamid, dipropylenglykols monometyleter, väts-keformiga polyoxietylenglykoler, propylenglykoi, 2-pyrrolidon, främst N-metyl-pyrrolidon, dietylenglykols monoetyieter, etylengiykol, dietylftalat elier en blandning av ätminstone tvä av dessa.
27. Användning enligt nagot av patentkraven 25 ooh 26, känne- t e c k n a d av att den dessutom omfattar ett organiskt hjälplösningsmedel (d), vars kokpunkt är under 100 °C och vars dielektricätetskonstant är 10-40 och som blandas I vatien och/eller Iösningsmedei (c), varvid detta hjäiplösnings-mede! företrädesvis är närvarande i hjälplösningsmediets (d):s och lösnings- 20 medlets (c):s vikt/vikt- (w/w) förhällande 1:15-1:2.
28. Användning enligt patentkrav 27, kännetecknad av att organiskt hjälplösningsmedels (d) kokpunkt är under 80 ÖC.
29. Användning enligt patentkrav 27 elier 28, kännetecknad av att organiskt hjälplösningsmedels (d) dieiektricitetskonstant är 20 - 30.
30. Användning enligt nagot av patentkraven 27-29, känne tecknad av att hjälplösningsmediet (d) väljs frän absoiut etanol, isopropa- C\J 5 nol och metanol. ^ 31. Användning enligt nagot av patentkraven 1, 2, 4, 6, 7 och 11 - 9 30, k ä n n e t e c k n a d av att komposition innebäller 5 -10 % av föreningen S 30 1-[2,6-Ci2-4-CF3-fenyl]-3-CN-4-[SO-CF3]-5-NH2-pyrazol och 5-20 % pyriproxi- a. fen. Q_ <-» 32. Användning enligt nagot av patentkraven 1, 2, 4, 6, 8 och 11 - ^ 30, k ä n n e te c k n a d av att komposition innehäller 10 % av föreningen 1- ^ [2,6-Ci2-4-CF3-fenyl]-3-CN-4-[SO-CF3]-5-NH2-pyrazol och 30 % metopren. CM
33, Användning enligt nägot av patentkraven 1-24, känne-t e c k n a d av att förening (A) är närvarande i komposition i en mängd 5 -15 % (w/v).
34, Användning enligt nagot av patentkraven 27 -33, känne-5 t e c k n a d av att det organiska iösningsmedlet (c) väljs frän N-metylpyrrolidon eller dietylenglykols monoetyleter, och bjälpiösningsmedlet (d) väljs frän absolut etanol, isopropanol och metanol.
35, Användning enligt nägot av patentkraven 16-34, kannele c k n a d av att kristalliseringsinhibitorn (b) omfattar polyvinylpyrrolidon.
36. Användning eniigt nägot av patentkraven 1-30, känne- tecknad av att den innehäller 5-15 % av föreningen 1-[2,6-Ci2-4-CF3-fenyl]-3-CN-4-ESO-CF3]-5-NH2-pyrazol och 1 - 20 % minst en förening (B).
37. Användning enligt patentkrav 36, k ä n n e t e c k n a d av att förening (B) är metopren. (M δ (M sj- o CO o X en CL O) O) δ δ (M
Applications Claiming Priority (6)
Application Number | Priority Date | Filing Date | Title |
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FR9604208 | 1996-03-29 | ||
FR9604208A FR2746594B1 (fr) | 1996-03-29 | 1996-03-29 | Association insecticide contre les puces des mammiferes, notamment des chiens et chats |
US69211396A | 1996-08-05 | 1996-08-05 | |
US69211396 | 1996-08-05 | ||
FR9700541 | 1997-01-20 | ||
PCT/FR1997/000541 WO1997036485A1 (fr) | 1996-03-29 | 1997-03-26 | Association insecticide contre les puces des mammiferes, notamment des chiens et chats |
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FI122765B true FI122765B (sv) | 2012-06-29 |
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FI974351A FI122468B (sv) | 1996-03-29 | 1997-11-27 | Insikticidkomposition mot däggdjurs, isynnerhet mot hundars och kattors loppor |
FI20115199A FI122765B (sv) | 1996-03-29 | 2011-02-28 | Insekticidkomposition för däggdjurs, i synnerhet för hundars och katters loppor |
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FI974351A FI122468B (sv) | 1996-03-29 | 1997-11-27 | Insikticidkomposition mot däggdjurs, isynnerhet mot hundars och kattors loppor |
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CL (1) | CL2004001187A1 (sv) |
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DE (15) | DE19782317A5 (sv) |
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FI (2) | FI122468B (sv) |
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