HUP0300464A2 - Inszekticid és akaricid tulajdonságú hatóanyag-kombinációk és alkalmazásuk - Google Patents
Inszekticid és akaricid tulajdonságú hatóanyag-kombinációk és alkalmazásukInfo
- Publication number
- HUP0300464A2 HUP0300464A2 HU0300464A HUP0300464A HUP0300464A2 HU P0300464 A2 HUP0300464 A2 HU P0300464A2 HU 0300464 A HU0300464 A HU 0300464A HU P0300464 A HUP0300464 A HU P0300464A HU P0300464 A2 HUP0300464 A2 HU P0300464A2
- Authority
- HU
- Hungary
- Prior art keywords
- alkyl
- optionally substituted
- group
- alkoxy
- phenyl
- Prior art date
Links
- 230000000895 acaricidal effect Effects 0.000 title 1
- 239000013543 active substance Substances 0.000 title 1
- 230000000749 insecticidal effect Effects 0.000 title 1
- 125000000217 alkyl group Chemical group 0.000 abstract 6
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 6
- 125000000547 substituted alkyl group Chemical group 0.000 abstract 6
- 125000004183 alkoxy alkyl group Chemical group 0.000 abstract 5
- 125000003545 alkoxy group Chemical group 0.000 abstract 5
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 abstract 4
- 125000003342 alkenyl group Chemical group 0.000 abstract 4
- 229910052760 oxygen Inorganic materials 0.000 abstract 4
- 239000001301 oxygen Substances 0.000 abstract 4
- 229910052717 sulfur Inorganic materials 0.000 abstract 4
- 125000004434 sulfur atom Chemical group 0.000 abstract 4
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 abstract 3
- 125000005843 halogen group Chemical group 0.000 abstract 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 3
- 125000003884 phenylalkyl group Chemical group 0.000 abstract 3
- 125000003282 alkyl amino group Chemical group 0.000 abstract 2
- 125000006350 alkyl thio alkyl group Chemical group 0.000 abstract 2
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 2
- 125000001188 haloalkyl group Chemical group 0.000 abstract 2
- 238000002360 preparation method Methods 0.000 abstract 2
- 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
- 239000005894 Emamectin Substances 0.000 abstract 1
- 239000005899 Fipronil Substances 0.000 abstract 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
- 239000005907 Indoxacarb Substances 0.000 abstract 1
- 239000005912 Lufenuron Substances 0.000 abstract 1
- 239000005917 Methoxyfenozide Substances 0.000 abstract 1
- 239000005937 Tebufenozide Substances 0.000 abstract 1
- 239000005938 Teflubenzuron Substances 0.000 abstract 1
- 241000256618 Trichogramma Species 0.000 abstract 1
- 239000005942 Triflumuron Substances 0.000 abstract 1
- 239000004480 active ingredient Substances 0.000 abstract 1
- 125000005108 alkenylthio 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
- 229910052785 arsenic Inorganic materials 0.000 abstract 1
- RQNWIZPPADIBDY-UHFFFAOYSA-N arsenic atom Chemical group [As] RQNWIZPPADIBDY-UHFFFAOYSA-N 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
- 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
- 150000001875 compounds Chemical class 0.000 abstract 1
- 125000004122 cyclic group Chemical group 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
- 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
- -1 diophenolan Chemical compound 0.000 abstract 1
- CXEGAUYXQAKHKJ-NSBHKLITSA-N emamectin B1a Chemical compound C1=C[C@H](C)[C@@H]([C@@H](C)CC)O[C@]11O[C@H](C\C=C(C)\[C@@H](O[C@@H]2O[C@@H](C)[C@H](O[C@@H]3O[C@@H](C)[C@H](NC)[C@@H](OC)C3)[C@@H](OC)C2)[C@@H](C)\C=C\C=C/2[C@]3([C@H](C(=O)O4)C=C(C)[C@@H](O)[C@H]3OC\2)O)C[C@H]4C1 CXEGAUYXQAKHKJ-NSBHKLITSA-N 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
- 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
- 229910052739 hydrogen Inorganic materials 0.000 abstract 1
- 239000001257 hydrogen Substances 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
- QCAWEPFNJXQPAN-UHFFFAOYSA-N methoxyfenozide Chemical compound COC1=CC=CC(C(=O)NN(C(=O)C=2C=C(C)C=C(C)C=2)C(C)(C)C)=C1C QCAWEPFNJXQPAN-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
- 125000005359 phenoxyalkyl group Chemical group 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
- QYPNKSZPJQQLRK-UHFFFAOYSA-N tebufenozide Chemical compound C1=CC(CC)=CC=C1C(=O)NN(C(C)(C)C)C(=O)C1=CC(C)=CC(C)=C1 QYPNKSZPJQQLRK-UHFFFAOYSA-N 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
- A01N43/12—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
- 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
- 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)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
Készítmény, amely (I) általános képletű ciklusos ketoenol - ahol Xhalogénatom, alkil-, alkoxi- vagy halogén-alkil-csoport; Y hidrogén-vagy halogénatom, III alkil-, alkoxi- vagy halogénalkil-csoport; Zalkil- vagy alkoxicsoport vagy halogénatom; n értéke 0-3; Ahidrogénatom vagy adott esetben szubsztituált alkil-, alkenil-,alkinil-, alkoxi-alkil-, polialkoxi-alkil-, alkil-tio-alkil- vagycikloalkilcsoport, amely oxigén- és/vagy kénatommal lehet megszakítva,éles adott esetben szubsztituált fenil- vagy fenil-alkil-csoport; Bhidrogénatom, alkil- vagy alkoxi-alkil-csoport; vagy ahol A és B aszénatommal együtt, gyűrűt képez, amely adott esetben oxigén- és/vagykénatommal van megszakítva, és adott esetben vagy benzo-kondenzált,vagy adott esetben szubsztituált fenilcsoport; G hidrogénatom, vagy(b), (c), (d), (e) vagy (f) képletű csoport, ahol R1 adott esetbenszubsztituált alkil-, alkenil-, alkoxi-alkil-, alkil-tio-alkil-,polialkoxi-alkil- vagy cikloalkilcsoport, amely oxigén- és/vagykénatommal lehet megszakítva; és adott esetben szubsztituált fenil-,fenil-alkil-, piridil-, pirimidil-, tiazolil- vagy pirazolilcsoport;vagy adott esetben szubsztituált fenoxi-alkil-csoport; R2 adottesetben szubsztituált alkil-, alkenil-, alkoxi-alkil- vagy polialkoxi-alkil-, fenil- vagy benzilcsoport; R3 adott esetben szubsztituáltalkil-, fenil- vagy benzilcsoport; R4 és R5 adott esetbenszubsztituált alkil-, alkoxi-, alkil-amino-, di(alkil-amino)-, alkil-,alkenil-tio-, alkinil-tio- vagy cikloalkil-tio-csoport, vagy adottesetben szubsztituált fenil-, fenoxi- vagy fenil-tio-csoport; R6 és R7adott esetben szubsztituált alkil-, alkoxi-, alkenil- vagy alkoxi-alkil-csoport, adott esetben szubsztituált fenilcsoport, adott esetbenszubsztituált benzilcsoport, vagy együtt 5- vagy 6-tagú gyűrűt képez,amely adott esetben oxigén- vagy kénatommal lehet megszakítva, ésadott esetben szubsztituált; és legalább egy következő vegyületbőláll: klórfluazuron, diflubenzuron, lufenuron, teflubenzuron,triflumuron, novaluron, flufenoxuron, hexaflumuron, emamektin, metoxi-fenozid, tebufenozid, halofenozid, endoszulfán, Trichlogramma spp.,Verticillium lecanii, fipronil, ciromazin, azadirachtin, diofenolán,indoxakarb, kromafenozid, bisztrifluoron. A találmány magában foglaljaa fenti hatóanyag-kombinációk kezelési és készítmény előállításieljárásokban való alkalmazását is. Ó
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE10018370A DE10018370A1 (de) | 2000-04-14 | 2000-04-14 | Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften |
PCT/EP2001/003713 WO2001078511A1 (de) | 2000-04-14 | 2001-04-02 | Wirkstoffkombinationen mit insektiziden und akariziden eigenschaften |
Publications (2)
Publication Number | Publication Date |
---|---|
HUP0300464A2 true HUP0300464A2 (hu) | 2003-07-28 |
HUP0300464A3 HUP0300464A3 (en) | 2003-10-28 |
Family
ID=7638632
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
HU0300464A HUP0300464A3 (en) | 2000-04-14 | 2001-04-02 | Active substance combinations with insecticidal and acaricidal properties and use thereof |
Country Status (20)
Country | Link |
---|---|
US (1) | US6919090B2 (hu) |
EP (1) | EP1276376B1 (hu) |
JP (1) | JP5002108B2 (hu) |
KR (1) | KR100745459B1 (hu) |
CN (1) | CN1217577C (hu) |
AR (1) | AR035032A1 (hu) |
AT (1) | ATE300176T1 (hu) |
AU (2) | AU2001258303B2 (hu) |
BR (1) | BR0110069A (hu) |
CA (2) | CA2405371C (hu) |
DE (2) | DE10018370A1 (hu) |
EG (1) | EG23237A (hu) |
ES (1) | ES2243492T3 (hu) |
HU (1) | HUP0300464A3 (hu) |
IL (2) | IL152010A0 (hu) |
MX (1) | MXPA02010123A (hu) |
PL (1) | PL357831A1 (hu) |
TW (1) | TWI228124B (hu) |
WO (1) | WO2001078511A1 (hu) |
ZA (1) | ZA200207473B (hu) |
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 |
EP2525658B1 (de) | 2010-01-22 | 2017-03-01 | Bayer Intellectual Property GmbH | Akarizide und/oder insektizide wirkstoffkombinationen |
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 |
CN105900985A (zh) * | 2012-08-30 | 2016-08-31 | 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 |
Family Cites Families (61)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
NO89105A (hu) * | 1954-06-18 | |||
US3264177A (en) * | 1964-02-17 | 1966-08-02 | Dow Chemical Co | Methods for the control of arachnids |
US5342958A (en) * | 1970-05-15 | 1994-08-30 | Solvay Duphar International Research B.V. | Organic compounds derived from urea or thiourea |
US3989842A (en) * | 1970-05-15 | 1976-11-02 | U.S. Philips Corporation | Certain substituted benzoyl urea insecticides |
US4166124A (en) * | 1970-05-15 | 1979-08-28 | U.S. Philips Corporation | Insecticidal 2,6-dihalobenzoyl urea derivatives |
US5245071A (en) * | 1970-05-15 | 1993-09-14 | Duphar International Research B.V. | Organic compounds derived from urea or thiourea |
US3933908A (en) * | 1970-05-15 | 1976-01-20 | U.S. Philips Corporation | Substituted benzoyl ureas |
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-
2000
- 2000-04-14 DE DE10018370A patent/DE10018370A1/de not_active Withdrawn
-
2001
- 2001-04-02 JP JP2001575823A patent/JP5002108B2/ja not_active Expired - Fee Related
- 2001-04-02 HU HU0300464A patent/HUP0300464A3/hu unknown
- 2001-04-02 CN CN018098835A patent/CN1217577C/zh not_active Expired - Lifetime
- 2001-04-02 BR BR0110069-6A patent/BR0110069A/pt not_active Application Discontinuation
- 2001-04-02 AU AU2001258303A patent/AU2001258303B2/en not_active Ceased
- 2001-04-02 US US10/257,235 patent/US6919090B2/en not_active Expired - Fee Related
- 2001-04-02 AU AU5830301A patent/AU5830301A/xx active Pending
- 2001-04-02 EP EP01931557A patent/EP1276376B1/de not_active Expired - Lifetime
- 2001-04-02 KR KR1020027013474A patent/KR100745459B1/ko not_active IP Right Cessation
- 2001-04-02 AT AT01931557T patent/ATE300176T1/de not_active IP Right Cessation
- 2001-04-02 MX MXPA02010123A patent/MXPA02010123A/es active IP Right Grant
- 2001-04-02 DE DE50106896T patent/DE50106896D1/de not_active Expired - Fee Related
- 2001-04-02 CA CA2405371A patent/CA2405371C/en not_active Expired - Fee Related
- 2001-04-02 ES ES01931557T patent/ES2243492T3/es not_active Expired - Lifetime
- 2001-04-02 WO PCT/EP2001/003713 patent/WO2001078511A1/de active IP Right Grant
- 2001-04-02 CA CA2715554A patent/CA2715554A1/en not_active Abandoned
- 2001-04-02 IL IL15201001A patent/IL152010A0/xx active IP Right Grant
- 2001-04-02 PL PL01357831A patent/PL357831A1/xx not_active Application Discontinuation
- 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 |
---|---|
EP1276376B1 (de) | 2005-07-27 |
JP2003530409A (ja) | 2003-10-14 |
IL152010A0 (en) | 2003-04-10 |
US20030185813A1 (en) | 2003-10-02 |
CN1430470A (zh) | 2003-07-16 |
CA2405371C (en) | 2011-01-04 |
HUP0300464A3 (en) | 2003-10-28 |
CN1217577C (zh) | 2005-09-07 |
DE50106896D1 (de) | 2005-09-01 |
DE10018370A1 (de) | 2001-10-18 |
AR035032A1 (es) | 2004-04-14 |
KR20020087127A (ko) | 2002-11-21 |
KR100745459B1 (ko) | 2007-08-03 |
EG23237A (en) | 2004-09-29 |
US6919090B2 (en) | 2005-07-19 |
CA2405371A1 (en) | 2001-10-25 |
WO2001078511A1 (de) | 2001-10-25 |
IL152010A (en) | 2007-02-11 |
BR0110069A (pt) | 2002-12-31 |
AU2001258303B2 (en) | 2005-03-10 |
EP1276376A1 (de) | 2003-01-22 |
CA2715554A1 (en) | 2001-10-25 |
ATE300176T1 (de) | 2005-08-15 |
ZA200207473B (en) | 2003-09-18 |
TWI228124B (en) | 2005-02-21 |
PL357831A1 (en) | 2004-07-26 |
MXPA02010123A (es) | 2003-04-25 |
ES2243492T3 (es) | 2005-12-01 |
JP5002108B2 (ja) | 2012-08-15 |
AU5830301A (en) | 2001-10-30 |
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