MX2007014770A - Composiciones concentradas versatiles de alta carga para el control de ectoparasitos. - Google Patents
Composiciones concentradas versatiles de alta carga para el control de ectoparasitos.Info
- Publication number
- MX2007014770A MX2007014770A MX2007014770A MX2007014770A MX2007014770A MX 2007014770 A MX2007014770 A MX 2007014770A MX 2007014770 A MX2007014770 A MX 2007014770A MX 2007014770 A MX2007014770 A MX 2007014770A MX 2007014770 A MX2007014770 A MX 2007014770A
- Authority
- MX
- Mexico
- Prior art keywords
- composition
- surfactant
- metaflumizone
- carrier solvent
- approximately
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 74
- 239000012141 concentrate Substances 0.000 title abstract description 13
- 244000078703 ectoparasite Species 0.000 title description 5
- 241001465754 Metazoa Species 0.000 claims abstract description 31
- 239000002904 solvent Substances 0.000 claims abstract description 25
- MIFOMMKAVSCNKQ-HWIUFGAZSA-N Metaflumizone Chemical compound C1=CC(OC(F)(F)F)=CC=C1NC(=O)N\N=C(C=1C=C(C=CC=1)C(F)(F)F)\CC1=CC=C(C#N)C=C1 MIFOMMKAVSCNKQ-HWIUFGAZSA-N 0.000 claims abstract description 24
- 239000005914 Metaflumizone Substances 0.000 claims abstract description 24
- 239000004094 surface-active agent Substances 0.000 claims abstract description 24
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 16
- 238000000034 method Methods 0.000 claims description 14
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 12
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N dimethyl sulfoxide Natural products CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 claims description 8
- 239000007921 spray Substances 0.000 claims description 8
- 241001494479 Pecora Species 0.000 claims description 6
- 239000004540 pour-on Substances 0.000 claims description 6
- 241000282326 Felis catus Species 0.000 claims description 5
- 208000015181 infectious disease Diseases 0.000 claims description 5
- 238000011200 topical administration Methods 0.000 claims description 5
- 206010061217 Infestation Diseases 0.000 claims description 4
- 241000283707 Capra Species 0.000 claims description 3
- 239000000654 additive Substances 0.000 claims description 3
- 230000000996 additive effect Effects 0.000 claims description 3
- 235000013305 food Nutrition 0.000 claims description 3
- LLHKCFNBLRBOGN-UHFFFAOYSA-N propylene glycol methyl ether acetate Chemical group COCC(C)OC(C)=O LLHKCFNBLRBOGN-UHFFFAOYSA-N 0.000 claims description 3
- 241000282994 Cervidae Species 0.000 claims description 2
- 239000003963 antioxidant agent Substances 0.000 claims description 2
- 239000000975 dye Substances 0.000 claims description 2
- 238000005187 foaming Methods 0.000 claims description 2
- 239000002736 nonionic surfactant Substances 0.000 claims description 2
- 239000003755 preservative agent Substances 0.000 claims description 2
- 241000282836 Camelus dromedarius Species 0.000 claims 1
- 239000006260 foam Substances 0.000 claims 1
- 239000003381 stabilizer Substances 0.000 claims 1
- 238000009472 formulation Methods 0.000 abstract description 27
- 206010014143 Ectoparasitic Infestations Diseases 0.000 abstract description 5
- 230000000699 topical effect Effects 0.000 abstract description 5
- 208000029380 parasitic ectoparasitic infectious disease Diseases 0.000 abstract description 2
- 241000238876 Acari Species 0.000 description 6
- 239000000243 solution Substances 0.000 description 6
- 239000004544 spot-on Substances 0.000 description 6
- 241000238421 Arthropoda Species 0.000 description 4
- 241000283690 Bos taurus Species 0.000 description 4
- 241000283086 Equidae Species 0.000 description 4
- 238000002360 preparation method Methods 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- 241000282472 Canis lupus familiaris Species 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- 241001674048 Phthiraptera Species 0.000 description 3
- 239000008389 polyethoxylated castor oil Substances 0.000 description 3
- MEJYDZQQVZJMPP-ULAWRXDQSA-N (3s,3ar,6r,6ar)-3,6-dimethoxy-2,3,3a,5,6,6a-hexahydrofuro[3,2-b]furan Chemical compound CO[C@H]1CO[C@@H]2[C@H](OC)CO[C@@H]21 MEJYDZQQVZJMPP-ULAWRXDQSA-N 0.000 description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- 241000238631 Hexapoda Species 0.000 description 2
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 2
- 239000003945 anionic surfactant Substances 0.000 description 2
- 239000003085 diluting agent Substances 0.000 description 2
- 230000003993 interaction Effects 0.000 description 2
- LXCFILQKKLGQFO-UHFFFAOYSA-N methylparaben Chemical compound COC(=O)C1=CC=C(O)C=C1 LXCFILQKKLGQFO-UHFFFAOYSA-N 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- 229920001983 poloxamer Polymers 0.000 description 2
- 150000003138 primary alcohols Chemical class 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- QELSKZZBTMNZEB-UHFFFAOYSA-N propylparaben Chemical compound CCCOC(=O)C1=CC=C(O)C=C1 QELSKZZBTMNZEB-UHFFFAOYSA-N 0.000 description 2
- 230000000717 retained effect Effects 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 238000011282 treatment Methods 0.000 description 2
- WEEGYLXZBRQIMU-UHFFFAOYSA-N 1,8-cineole Natural products C1CC2CCC1(C)OC2(C)C WEEGYLXZBRQIMU-UHFFFAOYSA-N 0.000 description 1
- WDQFELCEOPFLCZ-UHFFFAOYSA-N 1-(2-hydroxyethyl)pyrrolidin-2-one Chemical compound OCCN1CCCC1=O WDQFELCEOPFLCZ-UHFFFAOYSA-N 0.000 description 1
- NZJXADCEESMBPW-UHFFFAOYSA-N 1-methylsulfinyldecane Chemical compound CCCCCCCCCCS(C)=O NZJXADCEESMBPW-UHFFFAOYSA-N 0.000 description 1
- KRUABTDBQQLWLS-UHFFFAOYSA-N 1-methylsulfinyltetradecane Chemical compound CCCCCCCCCCCCCCS(C)=O KRUABTDBQQLWLS-UHFFFAOYSA-N 0.000 description 1
- CTTJWXVQRJUJQW-UHFFFAOYSA-N 2,2-dioctyl-3-sulfobutanedioic acid Chemical class CCCCCCCCC(C(O)=O)(C(C(O)=O)S(O)(=O)=O)CCCCCCCC CTTJWXVQRJUJQW-UHFFFAOYSA-N 0.000 description 1
- DFEMJYIRAXUQQB-UHFFFAOYSA-N 3-ethyloxolan-2-one Chemical compound CCC1CCOC1=O DFEMJYIRAXUQQB-UHFFFAOYSA-N 0.000 description 1
- HBTAOSGHCXUEKI-UHFFFAOYSA-N 4-chloro-n,n-dimethyl-3-nitrobenzenesulfonamide Chemical compound CN(C)S(=O)(=O)C1=CC=C(Cl)C([N+]([O-])=O)=C1 HBTAOSGHCXUEKI-UHFFFAOYSA-N 0.000 description 1
- 125000004801 4-cyanophenyl group Chemical group [H]C1=C([H])C(C#N)=C([H])C([H])=C1* 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- 241000271566 Aves Species 0.000 description 1
- 241000282832 Camelidae Species 0.000 description 1
- 241000692095 Cuterebra Species 0.000 description 1
- ABIKNKURIGPIRJ-UHFFFAOYSA-N DL-4-hydroxy caproic acid Chemical compound CCC(O)CCC(O)=O ABIKNKURIGPIRJ-UHFFFAOYSA-N 0.000 description 1
- WEEGYLXZBRQIMU-WAAGHKOSSA-N Eucalyptol Chemical compound C1C[C@H]2CC[C@]1(C)OC2(C)C WEEGYLXZBRQIMU-WAAGHKOSSA-N 0.000 description 1
- 241000282324 Felis Species 0.000 description 1
- 241001660203 Gasterophilus Species 0.000 description 1
- 241000257176 Hypoderma <fly> Species 0.000 description 1
- 150000008575 L-amino acids Chemical class 0.000 description 1
- 241000920471 Lucilia caesar Species 0.000 description 1
- 241000771994 Melophagus ovinus Species 0.000 description 1
- FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 description 1
- MMOXZBCLCQITDF-UHFFFAOYSA-N N,N-diethyl-m-toluamide Chemical compound CCN(CC)C(=O)C1=CC=CC(C)=C1 MMOXZBCLCQITDF-UHFFFAOYSA-N 0.000 description 1
- 229920002685 Polyoxyl 35CastorOil Polymers 0.000 description 1
- 241000283984 Rodentia Species 0.000 description 1
- 241000258242 Siphonaptera Species 0.000 description 1
- 206010040914 Skin reaction Diseases 0.000 description 1
- 241000282887 Suidae Species 0.000 description 1
- 239000001089 [(2R)-oxolan-2-yl]methanol Substances 0.000 description 1
- 239000013543 active substance Substances 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 239000000443 aerosol Substances 0.000 description 1
- -1 alkyl methyl sulfoxides Chemical class 0.000 description 1
- 239000003674 animal food additive Substances 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 230000037396 body weight Effects 0.000 description 1
- 239000003093 cationic surfactant Substances 0.000 description 1
- 210000004081 cilia Anatomy 0.000 description 1
- 229960005233 cineole Drugs 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 229940031578 diisopropyl adipate Drugs 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 229940113088 dimethylacetamide Drugs 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 230000009977 dual effect Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000003623 enhancer Substances 0.000 description 1
- 125000000219 ethylidene group Chemical group [H]C(=[*])C([H])([H])[H] 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- JBFHTYHTHYHCDJ-UHFFFAOYSA-N gamma-caprolactone Chemical compound CCC1CCC(=O)O1 JBFHTYHTHYHCDJ-UHFFFAOYSA-N 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 244000144980 herd Species 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 239000002917 insecticide Substances 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 235000010270 methyl p-hydroxybenzoate Nutrition 0.000 description 1
- 239000004292 methyl p-hydroxybenzoate Substances 0.000 description 1
- 229960002216 methylparaben Drugs 0.000 description 1
- 230000001617 migratory effect Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 229920000847 nonoxynol Polymers 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 239000003961 penetration enhancing agent Substances 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 230000035755 proliferation Effects 0.000 description 1
- 235000010232 propyl p-hydroxybenzoate Nutrition 0.000 description 1
- 239000004405 propyl p-hydroxybenzoate Substances 0.000 description 1
- 229960003415 propylparaben Drugs 0.000 description 1
- HNJBEVLQSNELDL-UHFFFAOYSA-N pyrrolidin-2-one Chemical compound O=C1CCCN1 HNJBEVLQSNELDL-UHFFFAOYSA-N 0.000 description 1
- 150000004040 pyrrolidinones Chemical class 0.000 description 1
- 231100000430 skin reaction Toxicity 0.000 description 1
- 230000035483 skin reaction Effects 0.000 description 1
- 239000011877 solvent mixture Substances 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 239000013589 supplement Substances 0.000 description 1
- BSYVTEYKTMYBMK-UHFFFAOYSA-N tetrahydrofurfuryl alcohol Chemical compound OCC1CCCO1 BSYVTEYKTMYBMK-UHFFFAOYSA-N 0.000 description 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/16—Amides, e.g. hydroxamic acids
- A61K31/17—Amides, e.g. hydroxamic acids having the group >N—C(O)—N< or >N—C(S)—N<, e.g. urea, thiourea, carmustine
- A61K31/175—Amides, e.g. hydroxamic acids having the group >N—C(O)—N< or >N—C(S)—N<, e.g. urea, thiourea, carmustine having the group, >N—C(O)—N=N— or, e.g. carbonohydrazides, carbazones, semicarbazides, semicarbazones; Thioanalogues 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
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/44—Oils, fats or waxes according to two or more groups of A61K47/02-A61K47/42; Natural or modified natural oils, fats or waxes, e.g. castor oil, polyethoxylated castor oil, montan wax, lignite, shellac, rosin, beeswax or lanolin
-
- 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
- A61K9/0017—Non-human animal skin, e.g. pour-on, spot-on
-
- 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
- A61K9/08—Solutions
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P33/00—Antiparasitic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P33/00—Antiparasitic agents
- A61P33/14—Ectoparasiticides, e.g. scabicides
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Chemical & Material Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Dentistry (AREA)
- Wood Science & Technology (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Engineering & Computer Science (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Tropical Medicine & Parasitology (AREA)
- Dermatology (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Medicinal Preparation (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US68394905P | 2005-05-24 | 2005-05-24 | |
| PCT/US2006/019284 WO2006127399A2 (en) | 2005-05-24 | 2006-05-18 | Versatile high load concentrate compositions comprising metaflumizone for control of ecto-parasites |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MX2007014770A true MX2007014770A (es) | 2008-02-20 |
Family
ID=36968719
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MX2007014770A MX2007014770A (es) | 2005-05-24 | 2006-05-18 | Composiciones concentradas versatiles de alta carga para el control de ectoparasitos. |
Country Status (26)
| Country | Link |
|---|---|
| US (1) | US7763267B2 (https=) |
| EP (1) | EP1896000B1 (https=) |
| JP (1) | JP5042997B2 (https=) |
| KR (1) | KR20080012949A (https=) |
| CN (1) | CN101180043B (https=) |
| AP (1) | AP2360A (https=) |
| AR (1) | AR059113A1 (https=) |
| AT (1) | ATE516023T1 (https=) |
| AU (1) | AU2006249423B2 (https=) |
| BR (1) | BRPI0610146A2 (https=) |
| CA (1) | CA2609057A1 (https=) |
| CY (1) | CY1111742T1 (https=) |
| DK (1) | DK1896000T3 (https=) |
| EA (1) | EA013682B1 (https=) |
| ES (1) | ES2367584T3 (https=) |
| IL (1) | IL187460A0 (https=) |
| MX (1) | MX2007014770A (https=) |
| NO (1) | NO20076004L (https=) |
| NZ (1) | NZ563525A (https=) |
| PL (1) | PL1896000T3 (https=) |
| PT (1) | PT1896000E (https=) |
| SI (1) | SI1896000T1 (https=) |
| TW (1) | TWI368505B (https=) |
| UA (1) | UA96415C2 (https=) |
| WO (1) | WO2006127399A2 (https=) |
| ZA (1) | ZA200710181B (https=) |
Families Citing this family (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| TWI350728B (en) * | 2004-10-08 | 2011-10-21 | Wyeth Corp | Amitraz compositions |
| US8744546B2 (en) | 2005-05-05 | 2014-06-03 | Dexcom, Inc. | Cellulosic-based resistance domain for an analyte sensor |
| US20060288955A1 (en) * | 2005-05-24 | 2006-12-28 | Wyeth | Device and method for controlling insects |
| US20100095900A1 (en) * | 2005-05-24 | 2010-04-22 | Wyeth Llc | Device and method for controlling insects |
| TW200846029A (en) * | 2007-02-09 | 2008-12-01 | Wyeth Corp | High dose, long-acting ectoparasiticide for extended control |
| CL2008001614A1 (es) * | 2007-06-05 | 2008-08-08 | Wyeth Corp | Composicion parasiticida veterinaria que comprende un disolvente que no contiene hidroxilo, un estabilizador, amitraz y opcionalmente una lactona macrociclica y miristato de isopropilo; y su uso para tratar o controlar una infestacion o infeccion par |
| WO2009035908A1 (en) * | 2007-09-11 | 2009-03-19 | Wyeth | Compositions and their use for the treatment of protozoal infections comprising metaflumi zone |
| WO2010096623A1 (en) * | 2009-02-23 | 2010-08-26 | Wyeth Llc | Improved-scent ectoparasiticidal formulation |
| GB0912975D0 (en) * | 2009-07-24 | 2009-09-02 | Syngenta Ltd | Formulations |
| KR20130130761A (ko) | 2010-12-27 | 2013-12-02 | 인터벳 인터내셔널 비.브이. | 국소 적용 이속사졸린 제제 |
| ES2711760T3 (es) * | 2011-01-04 | 2019-05-07 | Novaliq Gmbh | Emulsiones de aceite/agua que comprenden alcanos semifluorados |
| GB201101209D0 (en) | 2011-01-24 | 2011-03-09 | Syngenta Ltd | Formulation component |
| CN102657220A (zh) * | 2012-03-31 | 2012-09-12 | 广西田园生化股份有限公司 | 含氰氟虫腙与有机磷类杀虫剂的超低容量液剂 |
| US9703217B1 (en) * | 2016-03-25 | 2017-07-11 | Xerox Corporation | Toner compositions for magnetic ink character recognition |
| GB201707930D0 (en) * | 2017-05-17 | 2017-06-28 | Syngenta Participations Ag | Formulation component |
| CN107568214B (zh) * | 2017-09-28 | 2020-12-11 | 中国农业科学院农业环境与可持续发展研究所 | 一种农药固体纳米分散体及其制备方法 |
Family Cites Families (31)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3711606A (en) * | 1970-09-02 | 1973-01-16 | Crown Zellerbach Corp | Enhancing tissue penetration of physiologically active steroidal agents with dmso |
| DE2614841A1 (de) * | 1976-04-06 | 1977-10-20 | Bayer Ag | Neue pour-on-formulierungen von anthelmintika |
| CA1176167A (en) | 1980-03-06 | 1984-10-16 | John J. Windheuser | Use of n,n-diethyl-m-toluamide for enhancing skin permeation of bio-affecting agents |
| US4337330A (en) * | 1980-09-02 | 1982-06-29 | Union Carbide Corporation | Blends of water soluble polyethers and poly(hydroxyethers)s |
| US4560553A (en) | 1981-07-07 | 1985-12-24 | Merck & Co., Inc. | Use of eucalyptol for enhancing skin permeation of bio-affecting agents |
| GB8525447D0 (en) | 1985-10-16 | 1985-11-20 | Fbc Ltd | Pesticidal compositions |
| EP0273862B1 (de) * | 1986-12-05 | 1991-07-10 | Ciba-Geigy Ag | Ektoparasitizide nicht-wässrige Pour-on-Flüssigformulierung |
| US5116850A (en) | 1987-11-30 | 1992-05-26 | E. I. Du Pont De Nemours And Co. | Heterocyclic pyrazoline carboxanilides |
| DE69119301T2 (de) | 1990-06-16 | 1996-10-17 | Nihon Nohyaku Co Ltd | Hydrazincarboxamidderivate, Verfahren für ihre Herstellung und ihre Verwendung |
| EP0553284A1 (en) | 1990-10-05 | 1993-08-04 | E.I. Du Pont De Nemours And Company | Semicarbazone arthropodicides |
| EP0486937B1 (en) | 1990-11-17 | 1995-03-22 | Nihon Nohyaku Co., Ltd. | Hydrazone derivatives, processes for production thereof, and uses thereof |
| US5462938A (en) | 1990-12-21 | 1995-10-31 | Annus; Gary D. | Arthropodicidal oxadiazinyl, thiadiazinyl and triazinyl carboxanilides |
| US5250532A (en) | 1991-04-11 | 1993-10-05 | Dowelanco | 3,4,N-trisubstituted-4,5-dihydro-1H-pyrazole-1-carboxamides and their use as insecticides |
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2006
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- 2006-05-18 AP AP2007004240A patent/AP2360A/xx active
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