AR035032A1 - Composiciones insecticidas y acaricidas, empleo de mezclas para el control de las pestes animales, procedimiento para controlar las pestes animales, y procedimiento para la obtencion de composiciones insecticidas y acaricidas - Google Patents
Composiciones insecticidas y acaricidas, empleo de mezclas para el control de las pestes animales, procedimiento para controlar las pestes animales, y procedimiento para la obtencion de composiciones insecticidas y acaricidasInfo
- Publication number
- AR035032A1 AR035032A1 ARP010101700A ARP010101700A AR035032A1 AR 035032 A1 AR035032 A1 AR 035032A1 AR P010101700 A ARP010101700 A AR P010101700A AR P010101700 A ARP010101700 A AR P010101700A AR 035032 A1 AR035032 A1 AR 035032A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- halogen
- alkoxy
- optionally
- optionally substituted
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title abstract 5
- 239000000642 acaricide Substances 0.000 title 2
- 239000002917 insecticide Substances 0.000 title 2
- 229910052736 halogen Inorganic materials 0.000 abstract 39
- 150000002367 halogens Chemical class 0.000 abstract 27
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 17
- 125000000217 alkyl group Chemical group 0.000 abstract 11
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 abstract 10
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 7
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 5
- 125000004414 alkyl thio group Chemical group 0.000 abstract 4
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 4
- 229910052739 hydrogen Inorganic materials 0.000 abstract 4
- 239000001257 hydrogen Substances 0.000 abstract 4
- 229910052760 oxygen Inorganic materials 0.000 abstract 4
- 239000001301 oxygen Substances 0.000 abstract 4
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 abstract 3
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 abstract 3
- 229910052717 sulfur Inorganic materials 0.000 abstract 3
- 239000011593 sulfur Substances 0.000 abstract 3
- 125000003837 (C1-C20) alkyl group Chemical group 0.000 abstract 2
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 abstract 2
- 125000004209 (C1-C8) alkyl group Chemical group 0.000 abstract 2
- 125000003358 C2-C20 alkenyl group Chemical group 0.000 abstract 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 2
- 241000607479 Yersinia pestis Species 0.000 abstract 2
- 230000000895 acaricidal effect Effects 0.000 abstract 2
- 125000003342 alkenyl group Chemical group 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 2
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 2
- 150000002431 hydrogen Chemical class 0.000 abstract 2
- 230000000749 insecticidal effect Effects 0.000 abstract 2
- 125000006413 ring segment Chemical group 0.000 abstract 2
- 125000000027 (C1-C10) alkoxy group Chemical group 0.000 abstract 1
- 125000000008 (C1-C10) alkyl group Chemical group 0.000 abstract 1
- 125000004400 (C1-C12) alkyl group Chemical group 0.000 abstract 1
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 1
- ZDOOQPFIGYHZFV-UHFFFAOYSA-N 2-ethyl-4-[(4-phenoxyphenoxy)methyl]-1,3-dioxolane Chemical compound O1C(CC)OCC1COC(C=C1)=CC=C1OC1=CC=CC=C1 ZDOOQPFIGYHZFV-UHFFFAOYSA-N 0.000 abstract 1
- ZOCSXAVNDGMNBV-UHFFFAOYSA-N 5-amino-1-[2,6-dichloro-4-(trifluoromethyl)phenyl]-4-[(trifluoromethyl)sulfinyl]-1H-pyrazole-3-carbonitrile Chemical compound NC1=C(S(=O)C(F)(F)F)C(C#N)=NN1C1=C(Cl)C=C(C(F)(F)F)C=C1Cl ZOCSXAVNDGMNBV-UHFFFAOYSA-N 0.000 abstract 1
- 239000005878 Azadirachtin Substances 0.000 abstract 1
- 239000005887 Chromafenozide Substances 0.000 abstract 1
- 241001266001 Cordyceps confragosa Species 0.000 abstract 1
- 239000005891 Cyromazine Substances 0.000 abstract 1
- 239000005893 Diflubenzuron Substances 0.000 abstract 1
- 239000005899 Fipronil Substances 0.000 abstract 1
- 239000005907 Indoxacarb Substances 0.000 abstract 1
- 239000005912 Lufenuron Substances 0.000 abstract 1
- 239000005938 Teflubenzuron Substances 0.000 abstract 1
- 239000005942 Triflumuron Substances 0.000 abstract 1
- 125000005108 alkenylthio group Chemical group 0.000 abstract 1
- 125000003545 alkoxy group Chemical group 0.000 abstract 1
- 125000003282 alkyl amino group Chemical group 0.000 abstract 1
- 125000000304 alkynyl group Chemical group 0.000 abstract 1
- 125000005109 alkynylthio group Chemical group 0.000 abstract 1
- VEHPJKVTJQSSKL-UHFFFAOYSA-N azadirachtin Natural products O1C2(C)C(C3(C=COC3O3)O)CC3C21C1(C)C(O)C(OCC2(OC(C)=O)C(CC3OC(=O)C(C)=CC)OC(C)=O)C2C32COC(C(=O)OC)(O)C12 VEHPJKVTJQSSKL-UHFFFAOYSA-N 0.000 abstract 1
- FTNJWQUOZFUQQJ-IRYYUVNJSA-N azadirachtin A Natural products C([C@@H]([C@]1(C=CO[C@H]1O1)O)[C@]2(C)O3)[C@H]1[C@]23[C@]1(C)[C@H](O)[C@H](OC[C@@]2([C@@H](C[C@@H]3OC(=O)C(\C)=C/C)OC(C)=O)C(=O)OC)[C@@H]2[C@]32CO[C@@](C(=O)OC)(O)[C@@H]12 FTNJWQUOZFUQQJ-IRYYUVNJSA-N 0.000 abstract 1
- FTNJWQUOZFUQQJ-NDAWSKJSSA-N azadirachtin A Chemical compound C([C@@H]([C@]1(C=CO[C@H]1O1)O)[C@]2(C)O3)[C@H]1[C@]23[C@]1(C)[C@H](O)[C@H](OC[C@@]2([C@@H](C[C@@H]3OC(=O)C(\C)=C\C)OC(C)=O)C(=O)OC)[C@@H]2[C@]32CO[C@@](C(=O)OC)(O)[C@@H]12 FTNJWQUOZFUQQJ-NDAWSKJSSA-N 0.000 abstract 1
- 229910052799 carbon Inorganic materials 0.000 abstract 1
- 150000001721 carbon Chemical group 0.000 abstract 1
- UISUNVFOGSJSKD-UHFFFAOYSA-N chlorfluazuron Chemical compound FC1=CC=CC(F)=C1C(=O)NC(=O)NC(C=C1Cl)=CC(Cl)=C1OC1=NC=C(C(F)(F)F)C=C1Cl UISUNVFOGSJSKD-UHFFFAOYSA-N 0.000 abstract 1
- HPNSNYBUADCFDR-UHFFFAOYSA-N chromafenozide Chemical compound CC1=CC(C)=CC(C(=O)N(NC(=O)C=2C(=C3CCCOC3=CC=2)C)C(C)(C)C)=C1 HPNSNYBUADCFDR-UHFFFAOYSA-N 0.000 abstract 1
- 125000005366 cycloalkylthio group Chemical group 0.000 abstract 1
- LVQDKIWDGQRHTE-UHFFFAOYSA-N cyromazine Chemical compound NC1=NC(N)=NC(NC2CC2)=N1 LVQDKIWDGQRHTE-UHFFFAOYSA-N 0.000 abstract 1
- 229950000775 cyromazine Drugs 0.000 abstract 1
- 125000004663 dialkyl amino group Chemical group 0.000 abstract 1
- QQQYTWIFVNKMRW-UHFFFAOYSA-N diflubenzuron Chemical compound FC1=CC=CC(F)=C1C(=O)NC(=O)NC1=CC=C(Cl)C=C1 QQQYTWIFVNKMRW-UHFFFAOYSA-N 0.000 abstract 1
- 229940019503 diflubenzuron Drugs 0.000 abstract 1
- RDYMFSUJUZBWLH-SVWSLYAFSA-N endosulfan Chemical compound C([C@@H]12)OS(=O)OC[C@@H]1[C@]1(Cl)C(Cl)=C(Cl)[C@@]2(Cl)C1(Cl)Cl RDYMFSUJUZBWLH-SVWSLYAFSA-N 0.000 abstract 1
- 229940013764 fipronil Drugs 0.000 abstract 1
- RYLHNOVXKPXDIP-UHFFFAOYSA-N flufenoxuron Chemical compound C=1C=C(NC(=O)NC(=O)C=2C(=CC=CC=2F)F)C(F)=CC=1OC1=CC=C(C(F)(F)F)C=C1Cl RYLHNOVXKPXDIP-UHFFFAOYSA-N 0.000 abstract 1
- 125000004438 haloalkoxy group Chemical group 0.000 abstract 1
- CNKHSLKYRMDDNQ-UHFFFAOYSA-N halofenozide Chemical compound C=1C=CC=CC=1C(=O)N(C(C)(C)C)NC(=O)C1=CC=C(Cl)C=C1 CNKHSLKYRMDDNQ-UHFFFAOYSA-N 0.000 abstract 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 abstract 1
- VBCVPMMZEGZULK-NRFANRHFSA-N indoxacarb Chemical compound C([C@@]1(OC2)C(=O)OC)C3=CC(Cl)=CC=C3C1=NN2C(=O)N(C(=O)OC)C1=CC=C(OC(F)(F)F)C=C1 VBCVPMMZEGZULK-NRFANRHFSA-N 0.000 abstract 1
- 229960000521 lufenuron Drugs 0.000 abstract 1
- PWPJGUXAGUPAHP-UHFFFAOYSA-N lufenuron Chemical compound C1=C(Cl)C(OC(F)(F)C(C(F)(F)F)F)=CC(Cl)=C1NC(=O)NC(=O)C1=C(F)C=CC=C1F PWPJGUXAGUPAHP-UHFFFAOYSA-N 0.000 abstract 1
- NJPPVKZQTLUDBO-UHFFFAOYSA-N novaluron Chemical compound C1=C(Cl)C(OC(F)(F)C(OC(F)(F)F)F)=CC=C1NC(=O)NC(=O)C1=C(F)C=CC=C1F NJPPVKZQTLUDBO-UHFFFAOYSA-N 0.000 abstract 1
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 abstract 1
- 125000003356 phenylsulfanyl group Chemical group [*]SC1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 abstract 1
- 125000003226 pyrazolyl group Chemical group 0.000 abstract 1
- 125000004076 pyridyl group Chemical group 0.000 abstract 1
- 125000000714 pyrimidinyl group Chemical group 0.000 abstract 1
- 229920006395 saturated elastomer Polymers 0.000 abstract 1
- 125000004434 sulfur atom Chemical group 0.000 abstract 1
- CJDWRQLODFKPEL-UHFFFAOYSA-N teflubenzuron Chemical compound FC1=CC=CC(F)=C1C(=O)NC(=O)NC1=CC(Cl)=C(F)C(Cl)=C1F CJDWRQLODFKPEL-UHFFFAOYSA-N 0.000 abstract 1
- 125000000335 thiazolyl group Chemical group 0.000 abstract 1
- XAIPTRIXGHTTNT-UHFFFAOYSA-N triflumuron Chemical compound C1=CC(OC(F)(F)F)=CC=C1NC(=O)NC(=O)C1=CC=CC=C1Cl XAIPTRIXGHTTNT-UHFFFAOYSA-N 0.000 abstract 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
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/02—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms
- A01N43/04—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom
- A01N43/06—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom five-membered rings
- A01N43/08—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom five-membered rings with oxygen as the ring hetero 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
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/02—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms
- A01N43/04—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom
- A01N43/06—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom five-membered rings
- A01N43/12—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom five-membered rings condensed with a carbocyclic ring
-
- 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
-
- 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
- A01N2300/00—Combinations or mixtures of active ingredients covered by classes A01N27/00 - A01N65/48 with other active or formulation relevant ingredients, e.g. specific carrier materials or surfactants, covered by classes A01N25/00 - A01N65/48
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Dentistry (AREA)
- Wood Science & Technology (AREA)
- Environmental Sciences (AREA)
- Zoology (AREA)
- Engineering & Computer Science (AREA)
- Plant Pathology (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Veterinary Medicine (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Public Health (AREA)
- Chemical & Material Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Organic Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Tropical Medicine & Parasitology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Abstract
CComposición que contiene mezclas de compuestos de la fórmula (1) en la que X significa alquilo C1-6, halógeno, alcoxi C1-6 o halógenoalquilo C1-3; Y significa hidrógeno, alquilo C1-6, halógeno, alcoxi C1-6 o halógenoalquilo C1-3; Z significa alquilo C1-6, halógeno o alcoxi C1-6; n significa un número de 0 a 3; A significa hidrógeno o significa alquilo C1-12, alquenilo C3-8, alquinilo C3-8, alcoxi C1-10-alquilo C2-8, polialcoxi C1-8-alquilo C2-8, alquiltio C1-10-alquilo C2-8, de cadena lineal o de cadena ramificada, cicloalquilo con 3 a 8 átomos en el anillo, que puede estar interrumpido por oxígeno y/o por azufre, substituidos respectiva y opcionalmente con halógeno, y significa fenilo o fenil-alquilo C1-6 substituidos respectiva y opcionalmente con halógeno, con alquilo C1-6, con halógenoalquilo C1-6, con alcoxi C1-6, con halógenoalcoxi C1-6 o con nitro; B significa hidrógeno, alquilo C1-6 o alcoxi C1-6-alquilo C2-4, o donde A y B junto con el átomo de carbono, con el que están enlazados, forman un anillo con 3 a 8 miembros, saturado o insaturado, interrumpido opcionalmente por oxígeno y/o por azufre y substituido opcionalmente con halógeno, con alquilo C1-6, con alcoxi C1-6, con halógenoalquilo C1-4, con halógenoalcoxi C1-4, con alquiltio C1-4 o fenilo opcionalmente substituido, o está opcionalmente benzocondensado; G significa hidrógeno o significa los grupos -CO-R1, -SO2-R3, restos de fórmula (2), (3) ó (4), en los cuales R1 significa alquilo C1-20, alquenilo C2-20, alcoxi C1-8-alquilo C2-8, alquiltio C1-8-alquilo C2-8, polialcoxi C1-8-alquilo C2-8 o cicloalquilo con 3 a 8 átomos en el anillo, que puede estar interrumpido por átomos de oxígeno y/o de azufre, substituidos respectiva y opcionalmente con halógeno, significa fenilo substituido opcionalmente con halógeno, con nitro, con alquilo C1-6, con alcoxi C1-6, con halógenoalquilo C1-6 o con halógenoalcoxi C1-6, significa fenil-alquilo C1-6 substituido opcionalmente con halógeno, con alquilo C1-6, con alcoxi C1-6, con halógenoalquilo C1-6 o con halógenoalcoxi C1-6, significa piridilo, pirimidilo, tiazolilo o pirazolilo substituidos respectiva y opcionalmente con halógeno y/o con alquilo C1-6, significa fenoxi-alquilo C1-6 substituido opcionalmente con halógeno y/o con alquilo C1-6; R2 significa alquilo C1-20, alquenilo C2-20, alcoxi C1-8-alquilo C2-8 o polialcoxi C1-8-alquilo C2-8, substituidos respectiva y opcionalmente con halógeno, significa fenilo o bencilo substituidos respectiva y opcionalmente con halógeno, con nitro, con alquilo C1-6, con alcoxi C1-6 o con halógenoalquilo C1-6; R3 significa alquilo C1-8 substituido opcionalmente con halógeno, significa fenilo o bencilo substituidos respectiva y opcionalmente con alquilo C1-4, con halógeno, con halógenoalquilo C1-4, con alcoxi C1-4, con halógenoalcoxi C1-4, con nitro o con ciano; R4 y R5 independientemente entre sí, significan alquilo C1-8, alcoxi C1-8, alquilamino C1-8, dialquilamino C1-8, alquiltio C1-8, alqueniltio C2-5, alquiniltio C2-5 o cicloalquiltio C3-7, substituidos respectiva y opcionalmente con halógeno, significa fenilo, fenoxi o feniltio substituido respectiva y opcionalmente con halógeno, con nitro, con ciano, con alcoxi C1-4, con halógenoalcoxi C1-4, con alquiltio C1-4, con halógenoalquiltio C1-4, con alquilo C1-4 o con halógenoalquilo C1-4; R6 y R7 independientemente entre sí, significan alquilo C1-10, alcoxi C1-10, alquenilo C3-8 o alcoxi C1-8-alquilo C1-8, substituidos respectiva y opcionalmente con halógeno, significan fenilo substituido opcionalmente con halógeno, con halógenoalquilo C1-6, con alquilo C1-6 o con alcoxi C1-6, significan bencilo substituido opcionalmente con halógeno, con alquilo C1-6, con halógenoalquilo C1-6 o con alcoxi C1-6, o juntos significan un anillo con 5 ó 6 miembros interrumpido opcionalmente por oxígeno o por azufre, que puede estar substituido opcionalmente con alquilo C1-6, y al menos uno de los compuestos siguientes: Chlorfluazuron, Diflubenzuron, Lufenuron, Teflubenzuron, Triflumuron, Novaluron, Flufenoxuron, Hexaflumuron, Emamectin, Methoxyfenozide, Tebufenozide, Halofenozide, Endosulfan, Trichlogramma spp., Verticillium-lecanii, Fipronil, Cyromazine, Azadirachtin, Diofenolan, Indoxacarb, Chromafenozide, o Bistrifluoron; empleo de mezclas para el control de las pestes animales, procedimiento para controlar las pestes animales, y procedimiento para la obtención de composiciones insecticidas y acaricidas, que tienen propiedades insecticidas y acaricidas muy buenas.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE10018370A DE10018370A1 (de) | 2000-04-14 | 2000-04-14 | Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR035032A1 true AR035032A1 (es) | 2004-04-14 |
Family
ID=7638632
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP010101700A AR035032A1 (es) | 2000-04-14 | 2001-04-10 | Composiciones insecticidas y acaricidas, empleo de mezclas para el control de las pestes animales, procedimiento para controlar las pestes animales, y procedimiento para la obtencion de composiciones insecticidas y acaricidas |
Country Status (20)
| Country | Link |
|---|---|
| US (1) | US6919090B2 (es) |
| EP (1) | EP1276376B1 (es) |
| JP (1) | JP5002108B2 (es) |
| KR (1) | KR100745459B1 (es) |
| CN (1) | CN1217577C (es) |
| AR (1) | AR035032A1 (es) |
| AT (1) | ATE300176T1 (es) |
| AU (2) | AU2001258303B2 (es) |
| BR (1) | BR0110069A (es) |
| CA (2) | CA2405371C (es) |
| DE (2) | DE10018370A1 (es) |
| EG (1) | EG23237A (es) |
| ES (1) | ES2243492T3 (es) |
| HU (1) | HUP0300464A3 (es) |
| IL (2) | IL152010A0 (es) |
| MX (1) | MXPA02010123A (es) |
| PL (1) | PL357831A1 (es) |
| TW (1) | TWI228124B (es) |
| WO (1) | WO2001078511A1 (es) |
| ZA (1) | ZA200207473B (es) |
Families Citing this family (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20050192319A1 (en) * | 1996-09-19 | 2005-09-01 | Albert Boeckh | Spot-on formulations for combating parasites |
| DE19818732A1 (de) * | 1998-04-27 | 1999-10-28 | Bayer Ag | Arylphenylsubstituierte cyclische Ketoenole |
| DE19948129A1 (de) * | 1999-10-07 | 2001-04-12 | Bayer Ag | Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften |
| MY142815A (en) | 2004-02-19 | 2011-01-14 | Univ Florida | Use of molt-accelerating compounds, ecdysteroids, analogs thereof, and chitin synthesis inhibitors for controlling termites. |
| DE102006014481A1 (de) * | 2006-03-29 | 2007-10-04 | Bayer Cropscience Ag | Wirkstoffkombinationen mit insektiziden Eigenschaften |
| DE102006014482A1 (de) * | 2006-03-29 | 2007-10-04 | Bayer Cropscience Ag | Wirkstoffkombinationen mit insektiziden Eigenschaften |
| US8110608B2 (en) | 2008-06-05 | 2012-02-07 | Ecolab Usa Inc. | Solid form sodium lauryl sulfate (SLS) pesticide composition |
| BR112012018108A2 (pt) | 2010-01-22 | 2015-10-20 | Bayer Ip Gmbh | combinações acaricidas e/ou inseticidas de ingredientes ativos |
| US8968757B2 (en) | 2010-10-12 | 2015-03-03 | Ecolab Usa Inc. | Highly wettable, water dispersible, granules including two pesticides |
| CN103563961B (zh) * | 2012-08-05 | 2016-07-06 | 南京华洲药业有限公司 | 一种含噻虫啉和甲氧虫酰肼的复合杀虫组合物及其用途 |
| CN103621518A (zh) * | 2012-08-30 | 2014-03-12 | 陕西美邦农药有限公司 | 一种含螺甲螨酯与生物源类的农药组合物 |
| CN106942261A (zh) * | 2017-04-13 | 2017-07-14 | 青岛瀚生生物科技股份有限公司 | 具有杀虫杀螨活性的组合物及其应用 |
| CN109673643A (zh) * | 2018-08-21 | 2019-04-26 | 青岛瀚生生物科技股份有限公司 | 农用杀虫组合物及其应用 |
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-
2000
- 2000-04-14 DE DE10018370A patent/DE10018370A1/de not_active Withdrawn
-
2001
- 2001-04-02 ES ES01931557T patent/ES2243492T3/es not_active Expired - Lifetime
- 2001-04-02 CA CA2405371A patent/CA2405371C/en not_active Expired - Fee Related
- 2001-04-02 PL PL01357831A patent/PL357831A1/xx not_active Application Discontinuation
- 2001-04-02 DE DE50106896T patent/DE50106896D1/de not_active Expired - Fee Related
- 2001-04-02 US US10/257,235 patent/US6919090B2/en not_active Expired - Fee Related
- 2001-04-02 MX MXPA02010123A patent/MXPA02010123A/es active IP Right Grant
- 2001-04-02 AU AU2001258303A patent/AU2001258303B2/en not_active Ceased
- 2001-04-02 EP EP01931557A patent/EP1276376B1/de not_active Expired - Lifetime
- 2001-04-02 IL IL15201001A patent/IL152010A0/xx active IP Right Grant
- 2001-04-02 JP JP2001575823A patent/JP5002108B2/ja not_active Expired - Fee Related
- 2001-04-02 AU AU5830301A patent/AU5830301A/xx active Pending
- 2001-04-02 WO PCT/EP2001/003713 patent/WO2001078511A1/de not_active Ceased
- 2001-04-02 KR KR1020027013474A patent/KR100745459B1/ko not_active Expired - Fee Related
- 2001-04-02 BR BR0110069-6A patent/BR0110069A/pt not_active Application Discontinuation
- 2001-04-02 HU HU0300464A patent/HUP0300464A3/hu unknown
- 2001-04-02 AT AT01931557T patent/ATE300176T1/de not_active IP Right Cessation
- 2001-04-02 CN CN018098835A patent/CN1217577C/zh not_active Expired - Lifetime
- 2001-04-02 CA CA2715554A patent/CA2715554A1/en not_active Abandoned
- 2001-04-09 TW TW090108373A patent/TWI228124B/zh not_active IP Right Cessation
- 2001-04-10 AR ARP010101700A patent/AR035032A1/es not_active Application Discontinuation
- 2001-04-18 EG EG20010387A patent/EG23237A/xx active
-
2002
- 2002-09-18 ZA ZA200207473A patent/ZA200207473B/en unknown
- 2002-09-30 IL IL152010A patent/IL152010A/en not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| MXPA02010123A (es) | 2003-04-25 |
| CA2405371C (en) | 2011-01-04 |
| DE50106896D1 (de) | 2005-09-01 |
| EP1276376A1 (de) | 2003-01-22 |
| US6919090B2 (en) | 2005-07-19 |
| AU5830301A (en) | 2001-10-30 |
| ES2243492T3 (es) | 2005-12-01 |
| CN1430470A (zh) | 2003-07-16 |
| AU2001258303B2 (en) | 2005-03-10 |
| KR20020087127A (ko) | 2002-11-21 |
| KR100745459B1 (ko) | 2007-08-03 |
| JP2003530409A (ja) | 2003-10-14 |
| HUP0300464A3 (en) | 2003-10-28 |
| HUP0300464A2 (hu) | 2003-07-28 |
| CN1217577C (zh) | 2005-09-07 |
| PL357831A1 (en) | 2004-07-26 |
| IL152010A (en) | 2007-02-11 |
| ATE300176T1 (de) | 2005-08-15 |
| JP5002108B2 (ja) | 2012-08-15 |
| BR0110069A (pt) | 2002-12-31 |
| US20030185813A1 (en) | 2003-10-02 |
| EG23237A (en) | 2004-09-29 |
| IL152010A0 (en) | 2003-04-10 |
| ZA200207473B (en) | 2003-09-18 |
| DE10018370A1 (de) | 2001-10-18 |
| TWI228124B (en) | 2005-02-21 |
| WO2001078511A1 (de) | 2001-10-25 |
| EP1276376B1 (de) | 2005-07-27 |
| CA2405371A1 (en) | 2001-10-25 |
| CA2715554A1 (en) | 2001-10-25 |
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Legal Events
| Date | Code | Title | Description |
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| FA | Abandonment or withdrawal |