ES2239132T3 - Combinaciones de productos activos con propiedades insecticidas y acaricidas. - Google Patents
Combinaciones de productos activos con propiedades insecticidas y acaricidas.Info
- Publication number
- ES2239132T3 ES2239132T3 ES01925397T ES01925397T ES2239132T3 ES 2239132 T3 ES2239132 T3 ES 2239132T3 ES 01925397 T ES01925397 T ES 01925397T ES 01925397 T ES01925397 T ES 01925397T ES 2239132 T3 ES2239132 T3 ES 2239132T3
- Authority
- ES
- Spain
- Prior art keywords
- carbon atoms
- alkyl
- atoms
- carbon
- halogen
- 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.)
- Expired - Lifetime
Links
- 239000002917 insecticide Substances 0.000 title description 12
- 239000000642 acaricide Substances 0.000 title description 6
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 202
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 66
- 229910052736 halogen Inorganic materials 0.000 claims abstract description 61
- 125000003545 alkoxy group Chemical group 0.000 claims abstract description 60
- 150000002367 halogens Chemical class 0.000 claims abstract description 59
- 125000004429 atom Chemical group 0.000 claims abstract description 42
- 229910052799 carbon Inorganic materials 0.000 claims abstract description 37
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims abstract description 33
- 125000001188 haloalkyl group Chemical group 0.000 claims abstract description 33
- 239000000203 mixture Substances 0.000 claims abstract description 32
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract description 19
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 16
- 150000001875 compounds Chemical class 0.000 claims abstract description 16
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims abstract description 16
- 125000004438 haloalkoxy group Chemical group 0.000 claims abstract description 15
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 15
- 239000001257 hydrogen Substances 0.000 claims abstract description 15
- 125000003342 alkenyl group Chemical group 0.000 claims abstract description 13
- 125000004414 alkyl thio group Chemical group 0.000 claims abstract description 11
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims abstract description 11
- 229910052760 oxygen Inorganic materials 0.000 claims abstract description 11
- 239000001301 oxygen Substances 0.000 claims abstract description 11
- 229910052717 sulfur Inorganic materials 0.000 claims abstract description 8
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims abstract description 7
- 125000000753 cycloalkyl group Chemical group 0.000 claims abstract description 7
- 239000011593 sulfur Substances 0.000 claims abstract description 7
- 125000003884 phenylalkyl group Chemical group 0.000 claims abstract description 5
- 125000006413 ring segment Chemical group 0.000 claims abstract description 5
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract description 3
- 125000000304 alkynyl group Chemical group 0.000 claims abstract description 3
- 241001465754 Metazoa Species 0.000 claims description 14
- 241000607479 Yersinia pestis Species 0.000 claims description 12
- 230000000895 acaricidal effect Effects 0.000 claims description 11
- 150000002431 hydrogen Chemical class 0.000 claims description 10
- 238000000034 method Methods 0.000 claims description 9
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 8
- 230000000749 insecticidal effect Effects 0.000 claims description 8
- XGWIJUOSCAQSSV-XHDPSFHLSA-N (S,S)-hexythiazox Chemical compound S([C@H]([C@@H]1C)C=2C=CC(Cl)=CC=2)C(=O)N1C(=O)NC1CCCCC1 XGWIJUOSCAQSSV-XHDPSFHLSA-N 0.000 claims description 4
- SPBDXSGPUHCETR-JFUDTMANSA-N 8883yp2r6d Chemical compound O1[C@@H](C)[C@H](O)[C@@H](OC)C[C@@H]1O[C@@H]1[C@@H](OC)C[C@H](O[C@@H]2C(=C/C[C@@H]3C[C@@H](C[C@@]4(O[C@@H]([C@@H](C)CC4)C(C)C)O3)OC(=O)[C@@H]3C=C(C)[C@@H](O)[C@H]4OC\C([C@@]34O)=C/C=C/[C@@H]2C)/C)O[C@H]1C.C1C[C@H](C)[C@@H]([C@@H](C)CC)O[C@@]21O[C@H](C\C=C(C)\[C@@H](O[C@@H]1O[C@@H](C)[C@H](O[C@@H]3O[C@@H](C)[C@H](O)[C@@H](OC)C3)[C@@H](OC)C1)[C@@H](C)\C=C\C=C/1[C@]3([C@H](C(=O)O4)C=C(C)[C@@H](O)[C@H]3OC\1)O)C[C@H]4C2 SPBDXSGPUHCETR-JFUDTMANSA-N 0.000 claims description 4
- 150000001721 carbon Chemical group 0.000 claims description 4
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 4
- UOAMTSKGCBMZTC-UHFFFAOYSA-N dicofol Chemical compound C=1C=C(Cl)C=CC=1C(C(Cl)(Cl)Cl)(O)C1=CC=C(Cl)C=C1 UOAMTSKGCBMZTC-UHFFFAOYSA-N 0.000 claims description 4
- 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 claims description 4
- DMYHGDXADUDKCQ-UHFFFAOYSA-N fenazaquin Chemical compound C1=CC(C(C)(C)C)=CC=C1CCOC1=NC=NC2=CC=CC=C12 DMYHGDXADUDKCQ-UHFFFAOYSA-N 0.000 claims description 4
- ZLBGSRMUSVULIE-GSMJGMFJSA-N milbemycin A3 Chemical compound O1[C@H](C)[C@@H](C)CC[C@@]11O[C@H](C\C=C(C)\C[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 ZLBGSRMUSVULIE-GSMJGMFJSA-N 0.000 claims description 4
- ITKAIUGKVKDENI-UHFFFAOYSA-N pyrimidifen Chemical compound CC1=C(C)C(CCOCC)=CC=C1OCCNC1=NC=NC(CC)=C1Cl ITKAIUGKVKDENI-UHFFFAOYSA-N 0.000 claims description 4
- FBQQHUGEACOBDN-UHFFFAOYSA-N quinomethionate Chemical compound N1=C2SC(=O)SC2=NC2=CC(C)=CC=C21 FBQQHUGEACOBDN-UHFFFAOYSA-N 0.000 claims description 4
- 229920006395 saturated elastomer Polymers 0.000 claims description 4
- 125000004434 sulfur atom Chemical group 0.000 claims description 4
- MLGCXEBRWGEOQX-UHFFFAOYSA-N tetradifon Chemical compound C1=CC(Cl)=CC=C1S(=O)(=O)C1=CC(Cl)=C(Cl)C=C1Cl MLGCXEBRWGEOQX-UHFFFAOYSA-N 0.000 claims description 4
- AZSNMRSAGSSBNP-UHFFFAOYSA-N 22,23-dihydroavermectin B1a Natural products C1CC(C)C(C(C)CC)OC21OC(CC=C(C)C(OC1OC(C)C(OC3OC(C)C(O)C(OC)C3)C(OC)C1)C(C)C=CC=C1C3(C(C(=O)O4)C=C(C)C(O)C3OC1)O)CC4C2 AZSNMRSAGSSBNP-UHFFFAOYSA-N 0.000 claims description 3
- IBSREHMXUMOFBB-JFUDTMANSA-N 5u8924t11h Chemical compound O1[C@@H](C)[C@H](O)[C@@H](OC)C[C@@H]1O[C@@H]1[C@@H](OC)C[C@H](O[C@@H]2C(=C/C[C@@H]3C[C@@H](C[C@@]4(O3)C=C[C@H](C)[C@@H](C(C)C)O4)OC(=O)[C@@H]3C=C(C)[C@@H](O)[C@H]4OC\C([C@@]34O)=C/C=C/[C@@H]2C)/C)O[C@H]1C.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](O)[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 IBSREHMXUMOFBB-JFUDTMANSA-N 0.000 claims description 3
- 239000005660 Abamectin Substances 0.000 claims description 3
- JFLRKDZMHNBDQS-UCQUSYKYSA-N CC[C@H]1CCC[C@@H]([C@H](C(=O)C2=C[C@H]3[C@@H]4C[C@@H](C[C@H]4C(=C[C@H]3[C@@H]2CC(=O)O1)C)O[C@H]5[C@@H]([C@@H]([C@H]([C@@H](O5)C)OC)OC)OC)C)O[C@H]6CC[C@@H]([C@H](O6)C)N(C)C.CC[C@H]1CCC[C@@H]([C@H](C(=O)C2=C[C@H]3[C@@H]4C[C@@H](C[C@H]4C=C[C@H]3C2CC(=O)O1)O[C@H]5[C@@H]([C@@H]([C@H]([C@@H](O5)C)OC)OC)OC)C)O[C@H]6CC[C@@H]([C@H](O6)C)N(C)C Chemical compound CC[C@H]1CCC[C@@H]([C@H](C(=O)C2=C[C@H]3[C@@H]4C[C@@H](C[C@H]4C(=C[C@H]3[C@@H]2CC(=O)O1)C)O[C@H]5[C@@H]([C@@H]([C@H]([C@@H](O5)C)OC)OC)OC)C)O[C@H]6CC[C@@H]([C@H](O6)C)N(C)C.CC[C@H]1CCC[C@@H]([C@H](C(=O)C2=C[C@H]3[C@@H]4C[C@@H](C[C@H]4C=C[C@H]3C2CC(=O)O1)O[C@H]5[C@@H]([C@@H]([C@H]([C@@H](O5)C)OC)OC)OC)C)O[C@H]6CC[C@@H]([C@H](O6)C)N(C)C JFLRKDZMHNBDQS-UCQUSYKYSA-N 0.000 claims description 3
- 239000005656 Fenazaquin Substances 0.000 claims description 3
- 239000005661 Hexythiazox Substances 0.000 claims description 3
- 239000005918 Milbemectin Substances 0.000 claims description 3
- 239000005930 Spinosad Substances 0.000 claims description 3
- 229950008167 abamectin Drugs 0.000 claims description 3
- ONHBDDJJTDTLIR-UHFFFAOYSA-N azocyclotin Chemical compound C1CCCCC1[Sn](N1N=CN=C1)(C1CCCCC1)C1CCCCC1 ONHBDDJJTDTLIR-UHFFFAOYSA-N 0.000 claims description 3
- WCMMILVIRZAPLE-UHFFFAOYSA-M cyhexatin Chemical compound C1CCCCC1[Sn](C1CCCCC1)(O)C1CCCCC1 WCMMILVIRZAPLE-UHFFFAOYSA-M 0.000 claims description 3
- 229960002418 ivermectin Drugs 0.000 claims description 3
- 229940014213 spinosad Drugs 0.000 claims description 3
- HYVWIQDYBVKITD-UHFFFAOYSA-N tolylfluanid Chemical compound CN(C)S(=O)(=O)N(SC(F)(Cl)Cl)C1=CC=C(C)C=C1 HYVWIQDYBVKITD-UHFFFAOYSA-N 0.000 claims description 3
- 239000005653 Bifenazate Substances 0.000 claims description 2
- 239000005663 Pyridaben Substances 0.000 claims description 2
- 239000005658 Tebufenpyrad Substances 0.000 claims description 2
- 125000005108 alkenylthio group Chemical group 0.000 claims description 2
- 125000003282 alkyl amino group Chemical group 0.000 claims description 2
- 125000005109 alkynylthio group Chemical group 0.000 claims description 2
- 125000005605 benzo group Chemical group 0.000 claims description 2
- VHLKTXFWDRXILV-UHFFFAOYSA-N bifenazate Chemical compound C1=C(NNC(=O)OC(C)C)C(OC)=CC=C1C1=CC=CC=C1 VHLKTXFWDRXILV-UHFFFAOYSA-N 0.000 claims description 2
- CWFOCCVIPCEQCK-UHFFFAOYSA-N chlorfenapyr Chemical compound BrC1=C(C(F)(F)F)N(COCC)C(C=2C=CC(Cl)=CC=2)=C1C#N CWFOCCVIPCEQCK-UHFFFAOYSA-N 0.000 claims description 2
- 125000005366 cycloalkylthio group Chemical group 0.000 claims description 2
- WOWBFOBYOAGEEA-UHFFFAOYSA-N diafenthiuron Chemical compound CC(C)C1=C(NC(=S)NC(C)(C)C)C(C(C)C)=CC(OC=2C=CC=CC=2)=C1 WOWBFOBYOAGEEA-UHFFFAOYSA-N 0.000 claims description 2
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims description 2
- 125000005359 phenoxyalkyl group Chemical group 0.000 claims description 2
- 125000003356 phenylsulfanyl group Chemical group [*]SC1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims description 2
- 125000003226 pyrazolyl group Chemical group 0.000 claims description 2
- DWFZBUWUXWZWKD-UHFFFAOYSA-N pyridaben Chemical compound C1=CC(C(C)(C)C)=CC=C1CSC1=C(Cl)C(=O)N(C(C)(C)C)N=C1 DWFZBUWUXWZWKD-UHFFFAOYSA-N 0.000 claims description 2
- 125000004076 pyridyl group Chemical group 0.000 claims description 2
- 125000000714 pyrimidinyl group Chemical group 0.000 claims description 2
- 239000004094 surface-active agent Substances 0.000 claims description 2
- ZZYSLNWGKKDOML-UHFFFAOYSA-N tebufenpyrad Chemical compound CCC1=NN(C)C(C(=O)NCC=2C=CC(=CC=2)C(C)(C)C)=C1Cl ZZYSLNWGKKDOML-UHFFFAOYSA-N 0.000 claims description 2
- 125000000335 thiazolyl group Chemical group 0.000 claims description 2
- 239000005651 Acequinocyl Substances 0.000 claims 1
- QDRXWCAVUNHOGA-UHFFFAOYSA-N acequinocyl Chemical group C1=CC=C2C(=O)C(CCCCCCCCCCCC)=C(OC(C)=O)C(=O)C2=C1 QDRXWCAVUNHOGA-UHFFFAOYSA-N 0.000 claims 1
- 125000004435 hydrogen atom Chemical class [H]* 0.000 abstract 2
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- 235000012015 potatoes Nutrition 0.000 description 1
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- 238000001556 precipitation Methods 0.000 description 1
- STJLVHWMYQXCPB-UHFFFAOYSA-N propiconazole Chemical compound O1C(CCC)COC1(C=1C(=CC(Cl)=CC=1)Cl)CN1N=CN=C1 STJLVHWMYQXCPB-UHFFFAOYSA-N 0.000 description 1
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- WJSXSXUHWBSPEP-UHFFFAOYSA-N pyridine;triphenylborane Chemical compound C1=CC=NC=C1.C1=CC=CC=C1B(C=1C=CC=CC=1)C1=CC=CC=C1 WJSXSXUHWBSPEP-UHFFFAOYSA-N 0.000 description 1
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Classifications
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- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- 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
- 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)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
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| DE10013914A DE10013914A1 (de) | 2000-03-21 | 2000-03-21 | Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften |
| DE10013914 | 2000-03-21 |
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| ES2239132T3 true ES2239132T3 (es) | 2005-09-16 |
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| ES01925397T Expired - Lifetime ES2239132T3 (es) | 2000-03-21 | 2001-03-08 | Combinaciones de productos activos con propiedades insecticidas y acaricidas. |
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| WO (1) | WO2001070027A2 (cg-RX-API-DMAC7.html) |
| ZA (1) | ZA200206608B (cg-RX-API-DMAC7.html) |
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| 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 |
| DE10013914A1 (de) * | 2000-03-21 | 2001-09-27 | Bayer Ag | Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften |
| DE10015310A1 (de) * | 2000-03-28 | 2001-10-04 | Bayer Ag | Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften |
| DE10017881A1 (de) * | 2000-04-11 | 2001-10-25 | Bayer Ag | Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften |
| DE10018370A1 (de) * | 2000-04-14 | 2001-10-18 | Bayer Ag | Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften |
| AR036872A1 (es) | 2001-08-13 | 2004-10-13 | Du Pont | Compuesto de antranilamida, composicion que lo comprende y metodo para controlar una plaga de invertebrados |
| DE10330723A1 (de) * | 2003-07-08 | 2005-02-03 | Bayer Cropscience Ag | Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften |
| DE10353281A1 (de) * | 2003-11-14 | 2005-06-16 | Bayer Cropscience Ag | Wirkstoffkombination mit insektiziden und akariziden Eigenschaften |
| DE10356550A1 (de) * | 2003-12-04 | 2005-07-07 | Bayer Cropscience Ag | Wirkstoffkombinationen mit insektiziden Eigenschaften |
| DE102004001112A1 (de) * | 2004-01-07 | 2005-08-18 | Bayer Cropscience Ag | Wirkstoffkombinationen mit insektizide und akariziden Eigenschaften |
| US20090054470A1 (en) * | 2005-03-15 | 2009-02-26 | Jan Pieter Hendrik Bosselaers | Use of mitochondrial electron transport inhibitors to control fouling organisms |
| EP1890538B1 (en) * | 2005-05-26 | 2015-10-28 | Eli Lilly And Company | Improved fish production |
| DE102006008691A1 (de) * | 2006-02-24 | 2007-08-30 | Bayer Cropscience Ag | Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften |
| DE102006014480A1 (de) * | 2006-03-29 | 2007-10-04 | Bayer Cropscience Ag | Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften |
| CN100355342C (zh) * | 2006-08-18 | 2007-12-19 | 中国农业大学 | 农药组合物 |
| CN101795568A (zh) * | 2007-06-07 | 2010-08-04 | 达沃股份有限公司 | 外寄生物的防控 |
| US8110608B2 (en) | 2008-06-05 | 2012-02-07 | Ecolab Usa Inc. | Solid form sodium lauryl sulfate (SLS) pesticide composition |
| DK2343975T3 (da) * | 2008-09-22 | 2012-12-03 | Entarco Sa | Spinosyn-antibegroningssammensætninger, fremgangsmåder til deres anvendelse samt genstande beskyttet mod vedhæftning af biobegroningsorganismer |
| JP2011037760A (ja) | 2009-08-11 | 2011-02-24 | Sumitomo Chemical Co Ltd | 有害生物防除組成物 |
| RS55986B1 (sr) | 2010-01-22 | 2017-09-29 | Bayer Ip Gmbh | Akaricidne i/ili insekticidne kombinacije aktivnih supstanci |
| US8968757B2 (en) | 2010-10-12 | 2015-03-03 | Ecolab Usa Inc. | Highly wettable, water dispersible, granules including two pesticides |
| DE102011013556A1 (de) * | 2011-03-10 | 2012-09-13 | Clariant International Ltd. | Zusammensetzungen enthaltend Copolymere |
| CN102669120A (zh) * | 2012-04-12 | 2012-09-19 | 广东中迅农科股份有限公司 | 一种含有阿维菌素和螺甲螨酯的增效杀螨组合物 |
| CN102726404A (zh) * | 2012-06-09 | 2012-10-17 | 广东中迅农科股份有限公司 | 含有螺甲螨酯和唑螨酯的杀螨组合物 |
| CN105165882B (zh) * | 2012-06-27 | 2017-07-28 | 李炎 | 一种含灭螨醌的杀螨组合物 |
| CN103621549B (zh) * | 2012-08-25 | 2015-10-28 | 陕西美邦农药有限公司 | 一种杀螨组合物 |
| CN103621509B (zh) * | 2012-08-28 | 2015-10-21 | 陕西美邦农药有限公司 | 一种含螺甲螨酯的农药组合物 |
| 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 |
| CN103651484B (zh) * | 2012-08-31 | 2015-04-15 | 陕西美邦农药有限公司 | 一种含螺甲螨酯与氨基甲酸酯类的农药组合物 |
| CN103651548B (zh) * | 2012-09-04 | 2015-10-28 | 陕西美邦农药有限公司 | 一种含螺甲螨酯的杀虫组合物 |
| CN105685078B (zh) * | 2012-09-04 | 2018-07-10 | 陕西美邦农药有限公司 | 一种农药组合物 |
| CN103651469A (zh) * | 2012-09-04 | 2014-03-26 | 陕西美邦农药有限公司 | 一种农药组合物 |
| CN103039474A (zh) * | 2012-12-17 | 2013-04-17 | 广东中迅农科股份有限公司 | 含有螺甲螨酯和丁醚脲的杀螨组合物 |
| CN104585179B (zh) * | 2014-12-25 | 2017-12-12 | 广东中迅农科股份有限公司 | 一种含有吡螨胺和螺螨双酯的增效杀螨组合物 |
| CN105766911A (zh) * | 2016-03-31 | 2016-07-20 | 太仓市璜泾华南农机作业专业合作社 | 一种含螺环季酮酸类化合物和杀虫单的杀虫组合物 |
| CN105746570A (zh) * | 2016-03-31 | 2016-07-13 | 太仓市璜泾华南农机作业专业合作社 | 一种含螺环季酮酸类化合物和四氟苯菊酯的杀虫组合物 |
| CN107318866A (zh) * | 2016-04-28 | 2017-11-07 | 江苏龙灯化学有限公司 | 一种杀虫组合物 |
| 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 |
| KR20180003122U (ko) | 2018-10-23 | 2018-10-31 | 정인성 | 커넥터의 풀림 방지를 위한 잠금 기기 |
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| US2812281A (en) | 1953-11-14 | 1957-11-05 | Philips Corp | Polychloro-diphenylsulfones and the use of such compounds for combatting the stages in the development of mites |
| US2812280A (en) | 1954-04-20 | 1957-11-05 | Rohm & Haas | Preparation of bis (halophenyl) trichloroethanol |
| BE585312A (cg-RX-API-DMAC7.html) | 1958-12-16 | |||
| US3272854A (en) | 1963-07-18 | 1966-09-13 | Us Rubber Co | Cycloaliphatic sulfite esters |
| US3264177A (en) | 1964-02-17 | 1966-08-02 | Dow Chemical Co | Methods for the control of arachnids |
| US3639446A (en) | 1965-12-13 | 1972-02-01 | Geigy Chem Corp | 4 4'-dibromo- and 4-chloro-4'-bromobenzilic acid esters |
| US3657451A (en) | 1971-02-08 | 1972-04-18 | Shell Oil Co | Organo-tin miticides and method of using the same |
| US4174405A (en) | 1974-02-25 | 1979-11-13 | Uniroyal, Inc. | Thiophenes useful in control of acarids |
| US4055661A (en) | 1974-12-11 | 1977-10-25 | E. I. Du Pont De Nemours And Company | Miticidal and aphicidal method utilizing 2-higher alkyl-3-hydroxy-1,4-naphthoquinone carboxylic acid esters |
| US4070481A (en) | 1975-09-15 | 1978-01-24 | E. I. Du Pont De Nemours And Company | Substituted 2-higher alkyl-3-hydroxy-1,4-naphthoquinone carboxylic acid esters and their use as miticides |
| US4148918A (en) | 1974-05-10 | 1979-04-10 | E. I. Du Pont De Nemours And Company | Substituted 2-higher alkyl-3-hydroxy-1,4-naphthoquinone carboxylic acid esters and their use as miticides |
| US4053634A (en) | 1975-09-15 | 1977-10-11 | E. I. Du Pont De Nemours And Company | Miticidal and aphicidal method utilizing 2-higher alkyl-3-hydroxy-1,4-naphthoquinone carboxylic acid esters |
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-
2000
- 2000-03-21 DE DE10013914A patent/DE10013914A1/de not_active Withdrawn
-
2001
- 2001-03-08 CN CNA018065570A patent/CN1635834A/zh active Pending
- 2001-03-08 MX MXPA02009219A patent/MXPA02009219A/es active IP Right Grant
- 2001-03-08 US US10/221,970 patent/US6706758B2/en not_active Expired - Lifetime
- 2001-03-08 KR KR1020027011333A patent/KR100730000B1/ko not_active Expired - Lifetime
- 2001-03-08 WO PCT/EP2001/002610 patent/WO2001070027A2/de not_active Ceased
- 2001-03-08 EP EP01925397A patent/EP1267620B1/de not_active Expired - Lifetime
- 2001-03-08 BR BRPI0109346-0A patent/BR0109346B1/pt not_active IP Right Cessation
- 2001-03-08 JP JP2001568236A patent/JP2003528059A/ja active Pending
- 2001-03-08 AU AU2001252169A patent/AU2001252169A1/en not_active Abandoned
- 2001-03-08 ES ES01925397T patent/ES2239132T3/es not_active Expired - Lifetime
- 2001-03-08 DE DE50105775T patent/DE50105775D1/de not_active Expired - Fee Related
- 2001-03-20 EG EG20010273A patent/EG23228A/xx active
- 2001-03-21 TW TW090106526A patent/TWI257291B/zh not_active IP Right Cessation
- 2001-03-21 AR ARP010101319A patent/AR030555A1/es active IP Right Grant
-
2002
- 2002-08-19 ZA ZA200206608A patent/ZA200206608B/en unknown
-
2004
- 2004-01-27 US US10/765,249 patent/US7205289B2/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| KR100730000B1 (ko) | 2007-06-20 |
| DE10013914A1 (de) | 2001-09-27 |
| WO2001070027A2 (de) | 2001-09-27 |
| US6706758B2 (en) | 2004-03-16 |
| JP2003528059A (ja) | 2003-09-24 |
| TWI257291B (en) | 2006-07-01 |
| AU2001252169A1 (en) | 2001-10-03 |
| EP1267620A2 (de) | 2003-01-02 |
| KR20020079923A (ko) | 2002-10-19 |
| US20040186171A1 (en) | 2004-09-23 |
| CN1635834A (zh) | 2005-07-06 |
| DE50105775D1 (de) | 2005-05-04 |
| EP1267620B1 (de) | 2005-03-30 |
| MXPA02009219A (es) | 2003-05-23 |
| ZA200206608B (en) | 2003-08-19 |
| AR030555A1 (es) | 2003-08-27 |
| US20030114312A1 (en) | 2003-06-19 |
| US7205289B2 (en) | 2007-04-17 |
| WO2001070027A3 (de) | 2002-06-27 |
| BR0109346A (pt) | 2003-06-17 |
| EG23228A (en) | 2004-08-31 |
| BR0109346B1 (pt) | 2012-12-11 |
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