JPS588002A - 殺体外寄生虫噴霧処方物 - Google Patents
殺体外寄生虫噴霧処方物Info
- Publication number
 - JPS588002A JPS588002A JP57110062A JP11006282A JPS588002A JP S588002 A JPS588002 A JP S588002A JP 57110062 A JP57110062 A JP 57110062A JP 11006282 A JP11006282 A JP 11006282A JP S588002 A JPS588002 A JP S588002A
 - Authority
 - JP
 - Japan
 - Prior art keywords
 - formulation according
 - weight
 - active compound
 - parts
 - animal
 - 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.)
 - Granted
 
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 44
 - 239000007921 spray Substances 0.000 title claims description 13
 - 238000009472 formulation Methods 0.000 claims abstract description 37
 - 150000001875 compounds Chemical class 0.000 claims abstract description 32
 - 241001465754 Metazoa Species 0.000 claims abstract description 22
 - 239000003921 oil Substances 0.000 claims abstract description 18
 - 239000002904 solvent Substances 0.000 claims abstract description 10
 - 244000078703 ectoparasite Species 0.000 claims abstract description 4
 - 238000000034 method Methods 0.000 claims abstract description 4
 - 239000004606 Fillers/Extenders Substances 0.000 claims description 12
 - 235000014113 dietary fatty acids Nutrition 0.000 claims description 11
 - 239000000194 fatty acid Substances 0.000 claims description 11
 - 229930195729 fatty acid Natural products 0.000 claims description 11
 - -1 fatty acid esters Chemical class 0.000 claims description 10
 - ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 claims description 9
 - 239000002253 acid Substances 0.000 claims description 9
 - 150000004665 fatty acids Chemical class 0.000 claims description 7
 - LZCLXQDLBQLTDK-UHFFFAOYSA-N ethyl 2-hydroxypropanoate Chemical compound CCOC(=O)C(C)O LZCLXQDLBQLTDK-UHFFFAOYSA-N 0.000 claims description 6
 - 244000045947 parasite Species 0.000 claims description 6
 - UFTFJSFQGQCHQW-UHFFFAOYSA-N triformin Chemical compound O=COCC(OC=O)COC=O UFTFJSFQGQCHQW-UHFFFAOYSA-N 0.000 claims description 6
 - FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 claims description 5
 - 241000272525 Anas platyrhynchos Species 0.000 claims description 4
 - 239000003925 fat Substances 0.000 claims description 4
 - 244000144972 livestock Species 0.000 claims description 4
 - 229920006395 saturated elastomer Polymers 0.000 claims description 4
 - DKPFZGUDAPQIHT-UHFFFAOYSA-N Butyl acetate Natural products CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 claims description 3
 - 229940116333 ethyl lactate Drugs 0.000 claims description 3
 - 150000003626 triacylglycerols Chemical class 0.000 claims description 3
 - MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 claims description 2
 - RYYWUUFWQRZTIU-UHFFFAOYSA-K thiophosphate Chemical compound [O-]P([O-])([O-])=S RYYWUUFWQRZTIU-UHFFFAOYSA-K 0.000 claims description 2
 - AMQJEAYHLZJPGS-UHFFFAOYSA-N N-Pentanol Chemical compound CCCCCO AMQJEAYHLZJPGS-UHFFFAOYSA-N 0.000 claims 1
 - GXCLVBGFBYZDAG-UHFFFAOYSA-N N-[2-(1H-indol-3-yl)ethyl]-N-methylprop-2-en-1-amine Chemical compound CN(CCC1=CNC2=C1C=CC=C2)CC=C GXCLVBGFBYZDAG-UHFFFAOYSA-N 0.000 claims 1
 - 230000001984 ectoparasiticidal effect Effects 0.000 abstract 1
 - LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 14
 - 235000019198 oils Nutrition 0.000 description 13
 - LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 7
 - 235000019441 ethanol Nutrition 0.000 description 7
 - 239000000126 substance Substances 0.000 description 5
 - 238000011282 treatment Methods 0.000 description 5
 - 150000002148 esters Chemical class 0.000 description 4
 - 238000002360 preparation method Methods 0.000 description 4
 - 241000238876 Acari Species 0.000 description 3
 - ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
 - 239000004359 castor oil Substances 0.000 description 3
 - 235000019438 castor oil Nutrition 0.000 description 3
 - ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 3
 - WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 3
 - 229920002545 silicone oil Polymers 0.000 description 3
 - 238000012360 testing method Methods 0.000 description 3
 - XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
 - CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
 - 241000283690 Bos taurus Species 0.000 description 2
 - IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
 - OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical group OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 2
 - YXWCBRDRVXHABN-JCMHNJIXSA-N [cyano-(4-fluoro-3-phenoxyphenyl)methyl] 3-[(z)-2-chloro-2-(4-chlorophenyl)ethenyl]-2,2-dimethylcyclopropane-1-carboxylate Chemical compound C=1C=C(F)C(OC=2C=CC=CC=2)=CC=1C(C#N)OC(=O)C1C(C)(C)C1\C=C(/Cl)C1=CC=C(Cl)C=C1 YXWCBRDRVXHABN-JCMHNJIXSA-N 0.000 description 2
 - 230000000694 effects Effects 0.000 description 2
 - 230000001804 emulsifying effect Effects 0.000 description 2
 - 239000000839 emulsion Substances 0.000 description 2
 - RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
 - MVLVMROFTAUDAG-UHFFFAOYSA-N ethyl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC MVLVMROFTAUDAG-UHFFFAOYSA-N 0.000 description 2
 - 150000002191 fatty alcohols Chemical class 0.000 description 2
 - 150000002576 ketones Chemical class 0.000 description 2
 - 239000007788 liquid Substances 0.000 description 2
 - 238000004519 manufacturing process Methods 0.000 description 2
 - 239000011877 solvent mixture Substances 0.000 description 2
 - 238000005507 spraying Methods 0.000 description 2
 - WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
 - DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical class C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 description 1
 - RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
 - IIZPXYDJLKNOIY-JXPKJXOSSA-N 1-palmitoyl-2-arachidonoyl-sn-glycero-3-phosphocholine Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCC\C=C/C\C=C/C\C=C/C\C=C/CCCCC IIZPXYDJLKNOIY-JXPKJXOSSA-N 0.000 description 1
 - XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 description 1
 - TWJNQYPJQDRXPH-UHFFFAOYSA-N 2-cyanobenzohydrazide Chemical compound NNC(=O)C1=CC=CC=C1C#N TWJNQYPJQDRXPH-UHFFFAOYSA-N 0.000 description 1
 - LEACJMVNYZDSKR-UHFFFAOYSA-N 2-octyldodecan-1-ol Chemical compound CCCCCCCCCCC(CO)CCCCCCCC LEACJMVNYZDSKR-UHFFFAOYSA-N 0.000 description 1
 - LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 1
 - QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
 - 229920002134 Carboxymethyl cellulose Polymers 0.000 description 1
 - 206010007882 Cellulitis Diseases 0.000 description 1
 - LVGKNOAMLMIIKO-UHFFFAOYSA-N Elaidinsaeure-aethylester Natural products CCCCCCCCC=CCCCCCCCC(=O)OCC LVGKNOAMLMIIKO-UHFFFAOYSA-N 0.000 description 1
 - 108010010803 Gelatin Proteins 0.000 description 1
 - 229930194542 Keto Natural products 0.000 description 1
 - 235000021360 Myristic acid Nutrition 0.000 description 1
 - TUNFSRHWOTWDNC-UHFFFAOYSA-N Myristic acid Natural products CCCCCCCCCCCCCC(O)=O TUNFSRHWOTWDNC-UHFFFAOYSA-N 0.000 description 1
 - SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 1
 - 229910002651 NO3 Inorganic materials 0.000 description 1
 - NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 1
 - 239000005642 Oleic acid Substances 0.000 description 1
 - ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 1
 - 241000845082 Panama Species 0.000 description 1
 - 244000046052 Phaseolus vulgaris Species 0.000 description 1
 - 235000010627 Phaseolus vulgaris Nutrition 0.000 description 1
 - 241001474791 Proboscis Species 0.000 description 1
 - DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 description 1
 - HVUMOYIDDBPOLL-XWVZOOPGSA-N Sorbitan monostearate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O HVUMOYIDDBPOLL-XWVZOOPGSA-N 0.000 description 1
 - 229920002472 Starch Polymers 0.000 description 1
 - ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
 - 230000003187 abdominal effect Effects 0.000 description 1
 - 239000013543 active substance Substances 0.000 description 1
 - 239000002318 adhesion promoter Substances 0.000 description 1
 - 150000001298 alcohols Chemical class 0.000 description 1
 - 235000010443 alginic acid Nutrition 0.000 description 1
 - 229920000615 alginic acid Polymers 0.000 description 1
 - 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
 - 150000001409 amidines Chemical class 0.000 description 1
 - 239000002280 amphoteric surfactant Substances 0.000 description 1
 - 239000003945 anionic surfactant Substances 0.000 description 1
 - 239000003963 antioxidant agent Substances 0.000 description 1
 - 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
 - 238000003287 bathing Methods 0.000 description 1
 - OGBUMNBNEWYMNJ-UHFFFAOYSA-N batilol Chemical class CCCCCCCCCCCCCCCCCCOCC(O)CO OGBUMNBNEWYMNJ-UHFFFAOYSA-N 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
 - 210000000481 breast Anatomy 0.000 description 1
 - LRHPLDYGYMQRHN-UHFFFAOYSA-N butyl alcohol Substances CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 1
 - 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
 - CZBZUDVBLSSABA-UHFFFAOYSA-N butylated hydroxyanisole Chemical group COC1=CC=C(O)C(C(C)(C)C)=C1.COC1=CC=C(O)C=C1C(C)(C)C CZBZUDVBLSSABA-UHFFFAOYSA-N 0.000 description 1
 - 150000004657 carbamic acid derivatives Chemical class 0.000 description 1
 - 125000004432 carbon atom Chemical group C* 0.000 description 1
 - 239000001768 carboxy methyl cellulose Substances 0.000 description 1
 - 235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
 - 239000008112 carboxymethyl-cellulose Substances 0.000 description 1
 - 239000000969 carrier Substances 0.000 description 1
 - 239000003093 cationic surfactant Substances 0.000 description 1
 - 239000001913 cellulose Substances 0.000 description 1
 - 229920002678 cellulose Polymers 0.000 description 1
 - WOWHHFRSBJGXCM-UHFFFAOYSA-M cetyltrimethylammonium chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCC[N+](C)(C)C WOWHHFRSBJGXCM-UHFFFAOYSA-M 0.000 description 1
 - 239000012141 concentrate Substances 0.000 description 1
 - 238000007796 conventional method Methods 0.000 description 1
 - 229920001577 copolymer Polymers 0.000 description 1
 - 235000005687 corn oil Nutrition 0.000 description 1
 - 239000002537 cosmetic Substances 0.000 description 1
 - 235000012343 cottonseed oil Nutrition 0.000 description 1
 - 239000002385 cottonseed oil Substances 0.000 description 1
 - GVJHHUAWPYXKBD-UHFFFAOYSA-N d-alpha-tocopherol Natural products OC1=C(C)C(C)=C2OC(CCCC(C)CCCC(C)CCCC(C)C)(C)CCC2=C1C GVJHHUAWPYXKBD-UHFFFAOYSA-N 0.000 description 1
 - SASYSVUEVMOWPL-NXVVXOECSA-N decyl oleate Chemical compound CCCCCCCCCCOC(=O)CCCCCCC\C=C/CCCCCCCC SASYSVUEVMOWPL-NXVVXOECSA-N 0.000 description 1
 - 230000006866 deterioration Effects 0.000 description 1
 - 238000011161 development Methods 0.000 description 1
 - 210000005069 ears Anatomy 0.000 description 1
 - 239000003995 emulsifying agent Substances 0.000 description 1
 - 238000005516 engineering process Methods 0.000 description 1
 - 150000002170 ethers Chemical class 0.000 description 1
 - 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 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
 - 239000000835 fiber Substances 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
 - 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
 - 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
 - 238000007654 immersion Methods 0.000 description 1
 - 238000000338 in vitro Methods 0.000 description 1
 - 208000015181 infectious disease Diseases 0.000 description 1
 - 238000001802 infusion Methods 0.000 description 1
 - 229910001867 inorganic solvent Inorganic materials 0.000 description 1
 - 239000003049 inorganic solvent Substances 0.000 description 1
 - QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
 - 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
 - 125000000468 ketone group Chemical group 0.000 description 1
 - VMPHSYLJUKZBJJ-UHFFFAOYSA-N lauric acid triglyceride Natural products CCCCCCCCCCCC(=O)OCC(OC(=O)CCCCCCCCCCC)COC(=O)CCCCCCCCCCC VMPHSYLJUKZBJJ-UHFFFAOYSA-N 0.000 description 1
 - 235000010445 lecithin Nutrition 0.000 description 1
 - 239000000787 lecithin Substances 0.000 description 1
 - 229940067606 lecithin Drugs 0.000 description 1
 - 229920000609 methyl cellulose Polymers 0.000 description 1
 - UFEJKYYYVXYMMS-UHFFFAOYSA-N methylcarbamic acid Chemical compound CNC(O)=O UFEJKYYYVXYMMS-UHFFFAOYSA-N 0.000 description 1
 - 239000001923 methylcellulose Substances 0.000 description 1
 - 235000010981 methylcellulose Nutrition 0.000 description 1
 - 235000013336 milk Nutrition 0.000 description 1
 - 239000008267 milk Substances 0.000 description 1
 - 210000004080 milk Anatomy 0.000 description 1
 - 238000002156 mixing Methods 0.000 description 1
 - 239000002736 nonionic surfactant Substances 0.000 description 1
 - QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
 - WWZKQHOCKIZLMA-UHFFFAOYSA-N octanoic acid Chemical class CCCCCCCC(O)=O WWZKQHOCKIZLMA-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
 - BARWIPMJPCRCTP-CLFAGFIQSA-N oleyl oleate Chemical compound CCCCCCCC\C=C/CCCCCCCCOC(=O)CCCCCCC\C=C/CCCCCCCC BARWIPMJPCRCTP-CLFAGFIQSA-N 0.000 description 1
 - 239000003960 organic solvent Substances 0.000 description 1
 - 150000002903 organophosphorus compounds Chemical class 0.000 description 1
 - 230000003071 parasitic effect Effects 0.000 description 1
 - 230000024241 parasitism Effects 0.000 description 1
 - 210000002640 perineum Anatomy 0.000 description 1
 - XNGIFLGASWRNHJ-UHFFFAOYSA-L phthalate(2-) Chemical compound [O-]C(=O)C1=CC=CC=C1C([O-])=O XNGIFLGASWRNHJ-UHFFFAOYSA-L 0.000 description 1
 - 229920000058 polyacrylate Polymers 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
 - 238000007639 printing Methods 0.000 description 1
 - 235000003441 saturated fatty acids Nutrition 0.000 description 1
 - 150000004671 saturated fatty acids Chemical class 0.000 description 1
 - 239000008159 sesame oil Substances 0.000 description 1
 - 235000011803 sesame oil Nutrition 0.000 description 1
 - RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
 - 235000012239 silicon dioxide Nutrition 0.000 description 1
 - 238000002791 soaking Methods 0.000 description 1
 - 235000019333 sodium laurylsulphate Nutrition 0.000 description 1
 - 239000001587 sorbitan monostearate Substances 0.000 description 1
 - 235000011076 sorbitan monostearate Nutrition 0.000 description 1
 - 229940035048 sorbitan monostearate Drugs 0.000 description 1
 - 241000894007 species Species 0.000 description 1
 - 239000004551 spreading oil Substances 0.000 description 1
 - 239000003381 stabilizer Substances 0.000 description 1
 - 239000008107 starch Substances 0.000 description 1
 - 235000019698 starch Nutrition 0.000 description 1
 - 230000003068 static effect Effects 0.000 description 1
 - 238000003756 stirring Methods 0.000 description 1
 - 239000004094 surface-active agent Substances 0.000 description 1
 - 239000000725 suspension Substances 0.000 description 1
 - 229920003002 synthetic resin Polymers 0.000 description 1
 - 239000000057 synthetic resin Substances 0.000 description 1
 - OULAJFUGPPVRBK-UHFFFAOYSA-N tetratriacontan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCO OULAJFUGPPVRBK-UHFFFAOYSA-N 0.000 description 1
 - 150000003585 thioureas Chemical class 0.000 description 1
 - 229960001295 tocopherol Drugs 0.000 description 1
 - 229930003799 tocopherol Natural products 0.000 description 1
 - 235000010384 tocopherol Nutrition 0.000 description 1
 - 239000011732 tocopherol Substances 0.000 description 1
 - 125000002640 tocopherol group Chemical group 0.000 description 1
 - 150000004670 unsaturated fatty acids Chemical class 0.000 description 1
 - 235000021122 unsaturated fatty acids Nutrition 0.000 description 1
 - 235000013311 vegetables Nutrition 0.000 description 1
 - 239000001993 wax Substances 0.000 description 1
 - 230000004580 weight loss Effects 0.000 description 1
 - 239000000080 wetting agent 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
 - 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
 
 - 
        
- 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
 - 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
 
 
Landscapes
- Life Sciences & Earth Sciences (AREA)
 - General Health & Medical Sciences (AREA)
 - Health & Medical Sciences (AREA)
 - Toxicology (AREA)
 - Pest Control & Pesticides (AREA)
 - Plant Pathology (AREA)
 - Agronomy & Crop Science (AREA)
 - Engineering & Computer Science (AREA)
 - Dentistry (AREA)
 - Wood Science & Technology (AREA)
 - Zoology (AREA)
 - Environmental Sciences (AREA)
 - Agricultural Chemicals And Associated Chemicals (AREA)
 - Medicinal Preparation (AREA)
 - Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
 
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title | 
|---|---|---|---|
| DE3125897.2 | 1981-07-01 | ||
| DE19813125897 DE3125897A1 (de) | 1981-07-01 | 1981-07-01 | Ektoparasitizide sprueh-formulierungen | 
Publications (2)
| Publication Number | Publication Date | 
|---|---|
| JPS588002A true JPS588002A (ja) | 1983-01-18 | 
| JPH0113681B2 JPH0113681B2 (forum.php) | 1989-03-07 | 
Family
ID=6135829
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date | 
|---|---|---|---|
| JP57110062A Granted JPS588002A (ja) | 1981-07-01 | 1982-06-28 | 殺体外寄生虫噴霧処方物 | 
Country Status (11)
| Country | Link | 
|---|---|
| EP (1) | EP0069269B1 (forum.php) | 
| JP (1) | JPS588002A (forum.php) | 
| KR (1) | KR840000171A (forum.php) | 
| AT (1) | ATE21478T1 (forum.php) | 
| AU (1) | AU560431B2 (forum.php) | 
| DE (2) | DE3125897A1 (forum.php) | 
| DK (1) | DK294882A (forum.php) | 
| IL (1) | IL66147A0 (forum.php) | 
| NZ (1) | NZ201086A (forum.php) | 
| PH (1) | PH18948A (forum.php) | 
| ZA (1) | ZA824663B (forum.php) | 
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title | 
|---|---|---|---|---|
| JP2006213616A (ja) * | 2005-02-02 | 2006-08-17 | Osaka Seiyaku:Kk | 動物用外部寄生虫防除剤 | 
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title | 
|---|---|---|---|---|
| DE3529693A1 (de) * | 1985-08-20 | 1987-02-26 | Bayer Ag | Verfahren zur bekaempfung von ektoparasiten bei herdentieren und vergesellschaftet lebenden tieren | 
| DE4334553C2 (de) * | 1993-10-11 | 1998-05-20 | Synopharm Gmbh Pharmazeutische | Flüssiges pharmazeutisches System zur perkutanen Applikation | 
| IL147829A0 (en) * | 1999-08-12 | 2002-08-14 | Lilly Co Eli | Topical organic ectoparasiticidal formulations | 
| US6933318B1 (en) | 1999-08-12 | 2005-08-23 | Eli Lilly And Company | Topical organic ectoparasiticidal formulations | 
| AUPQ441699A0 (en) * | 1999-12-02 | 2000-01-06 | Eli Lilly And Company | Pour-on formulations | 
| DE10063865A1 (de) * | 2000-12-21 | 2002-06-27 | Bayer Ag | Verwendung von Pyrazoloximen als Parasitizide | 
| DK1435786T3 (da) | 2001-09-17 | 2011-10-03 | Lilly Co Eli | Pesticide formuleringer | 
| KR100758371B1 (ko) * | 2006-08-10 | 2007-09-14 | 한국생명공학연구원 | 살충제 | 
| GB201205562D0 (en) * | 2012-03-29 | 2012-05-09 | Reckitt & Colman Overseas | Liquid insecticidal compositions | 
| CN103141505B (zh) * | 2013-03-29 | 2015-04-22 | 广西田园生化股份有限公司 | 一种防治水稻稻飞虱的展膜油剂组合药剂 | 
| CN103355287A (zh) * | 2013-07-30 | 2013-10-23 | 河北博嘉农业有限公司 | 一种防治稻水象甲的展膜油剂 | 
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title | 
|---|---|---|---|---|
| DE1542752A1 (de) * | 1965-12-18 | 1970-07-30 | Jenapharm Veb | Mittel zu Bekaempfung von Ekto- und Endoparasiten bei Warmbluetern und Verfahren zu ihrer Herstellung | 
| DE2614841A1 (de) * | 1976-04-06 | 1977-10-20 | Bayer Ag | Neue pour-on-formulierungen von anthelmintika | 
| IT1123122B (it) * | 1979-09-12 | 1986-04-30 | Montedison Spa | Composizioni liquide insetticide contenenti piretroidi sintetici | 
| DE3029426A1 (de) * | 1980-08-02 | 1982-03-11 | Bayer Ag, 5090 Leverkusen | Gegen zwecken wirksame pour-on-formulierungen | 
| US4479968A (en) * | 1980-10-17 | 1984-10-30 | The Wellcome Foundation Ltd. | Control of ectoparasitic infestations of pigs | 
| EP0061208A1 (en) * | 1981-03-16 | 1982-09-29 | Janssen Pharmaceutica N.V. | Insecticidal control of ectoparasites | 
- 
        1981
        
- 1981-07-01 DE DE19813125897 patent/DE3125897A1/de not_active Withdrawn
 
 - 
        1982
        
- 1982-06-21 EP EP82105418A patent/EP0069269B1/de not_active Expired
 - 1982-06-21 DE DE8282105418T patent/DE3272717D1/de not_active Expired
 - 1982-06-21 AT AT82105418T patent/ATE21478T1/de active
 - 1982-06-24 PH PH27482A patent/PH18948A/en unknown
 - 1982-06-28 JP JP57110062A patent/JPS588002A/ja active Granted
 - 1982-06-28 IL IL66147A patent/IL66147A0/xx unknown
 - 1982-06-28 NZ NZ201086A patent/NZ201086A/en unknown
 - 1982-06-30 AU AU85466/82A patent/AU560431B2/en not_active Ceased
 - 1982-06-30 ZA ZA824663A patent/ZA824663B/xx unknown
 - 1982-06-30 DK DK294882A patent/DK294882A/da unknown
 - 1982-07-01 KR KR1019820002951A patent/KR840000171A/ko not_active Withdrawn
 
 
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title | 
|---|---|---|---|---|
| JP2006213616A (ja) * | 2005-02-02 | 2006-08-17 | Osaka Seiyaku:Kk | 動物用外部寄生虫防除剤 | 
Also Published As
| Publication number | Publication date | 
|---|---|
| ATE21478T1 (de) | 1986-09-15 | 
| DK294882A (da) | 1983-01-02 | 
| EP0069269A3 (en) | 1984-04-25 | 
| PH18948A (en) | 1985-11-14 | 
| AU8546682A (en) | 1983-01-06 | 
| DE3125897A1 (de) | 1983-02-10 | 
| DE3272717D1 (de) | 1986-09-25 | 
| KR840000171A (ko) | 1984-02-18 | 
| IL66147A0 (en) | 1982-09-30 | 
| EP0069269B1 (de) | 1986-08-20 | 
| EP0069269A2 (de) | 1983-01-12 | 
| JPH0113681B2 (forum.php) | 1989-03-07 | 
| ZA824663B (en) | 1983-04-27 | 
| AU560431B2 (en) | 1987-04-09 | 
| NZ201086A (en) | 1986-04-11 | 
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