UA78280C2 - Засіб для боротьби з шкідниками тварин - Google Patents
Засіб для боротьби з шкідниками тварин Download PDFInfo
- Publication number
- UA78280C2 UA78280C2 UA20040807169A UA20040807169A UA78280C2 UA 78280 C2 UA78280 C2 UA 78280C2 UA 20040807169 A UA20040807169 A UA 20040807169A UA 20040807169 A UA20040807169 A UA 20040807169A UA 78280 C2 UA78280 C2 UA 78280C2
- Authority
- UA
- Ukraine
- Prior art keywords
- active substances
- emulsifier
- solvent
- clothianidin
- spp
- Prior art date
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- 241000607479 Yersinia pestis Species 0.000 title claims description 15
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- IHTAIAZIELSSOO-MKWAYWHRSA-N sodium (Z)-hydroxyimino-(1-hydroxypropan-2-yl)-oxidoazanium Chemical compound [Na+].CC(CO)[N+](\[O-])=N\O IHTAIAZIELSSOO-MKWAYWHRSA-N 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- IYYIUOWKEMQYNV-UHFFFAOYSA-N sodium;ethoxy-oxido-oxophosphanium Chemical compound [Na+].CCO[P+]([O-])=O IYYIUOWKEMQYNV-UHFFFAOYSA-N 0.000 description 1
- 239000011877 solvent mixture Substances 0.000 description 1
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- 125000003003 spiro group Chemical group 0.000 description 1
- DTDSAWVUFPGDMX-UHFFFAOYSA-N spirodiclofen Chemical compound CCC(C)(C)C(=O)OC1=C(C=2C(=CC(Cl)=CC=2)Cl)C(=O)OC11CCCCC1 DTDSAWVUFPGDMX-UHFFFAOYSA-N 0.000 description 1
- GOLXNESZZPUPJE-UHFFFAOYSA-N spiromesifen Chemical compound CC1=CC(C)=CC(C)=C1C(C(O1)=O)=C(OC(=O)CC(C)(C)C)C11CCCC1 GOLXNESZZPUPJE-UHFFFAOYSA-N 0.000 description 1
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- 229960005322 streptomycin Drugs 0.000 description 1
- 150000004763 sulfides Chemical class 0.000 description 1
- 229940124530 sulfonamide Drugs 0.000 description 1
- XIUROWKZWPIAIB-UHFFFAOYSA-N sulfotep Chemical compound CCOP(=S)(OCC)OP(=S)(OCC)OCC XIUROWKZWPIAIB-UHFFFAOYSA-N 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 150000003464 sulfur compounds Chemical class 0.000 description 1
- JXHJNEJVUNHLKO-UHFFFAOYSA-N sulprofos Chemical compound CCCSP(=S)(OCC)OC1=CC=C(SC)C=C1 JXHJNEJVUNHLKO-UHFFFAOYSA-N 0.000 description 1
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- 229910052623 talc Inorganic materials 0.000 description 1
- 239000011269 tar Substances 0.000 description 1
- 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 description 1
- ROZUQUDEWZIBHV-UHFFFAOYSA-N tecloftalam Chemical compound OC(=O)C1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1C(=O)NC1=CC=CC(Cl)=C1Cl ROZUQUDEWZIBHV-UHFFFAOYSA-N 0.000 description 1
- XQTLDIFVVHJORV-UHFFFAOYSA-N tecnazene Chemical compound [O-][N+](=O)C1=C(Cl)C(Cl)=CC(Cl)=C1Cl XQTLDIFVVHJORV-UHFFFAOYSA-N 0.000 description 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 description 1
- WWJZWCUNLNYYAU-UHFFFAOYSA-N temephos Chemical compound C1=CC(OP(=S)(OC)OC)=CC=C1SC1=CC=C(OP(=S)(OC)OC)C=C1 WWJZWCUNLNYYAU-UHFFFAOYSA-N 0.000 description 1
- IROINLKCQGIITA-UHFFFAOYSA-N terbutryn Chemical compound CCNC1=NC(NC(C)(C)C)=NC(SC)=N1 IROINLKCQGIITA-UHFFFAOYSA-N 0.000 description 1
- IWVCMVBTMGNXQD-UHFFFAOYSA-N terramycin dehydrate Natural products C1=CC=C2C(O)(C)C3C(O)C4C(N(C)C)C(O)=C(C(N)=O)C(=O)C4(O)C(O)=C3C(=O)C2=C1O IWVCMVBTMGNXQD-UHFFFAOYSA-N 0.000 description 1
- UBCKGWBNUIFUST-YHYXMXQVSA-N tetrachlorvinphos Chemical compound COP(=O)(OC)O\C(=C/Cl)C1=CC(Cl)=C(Cl)C=C1Cl UBCKGWBNUIFUST-YHYXMXQVSA-N 0.000 description 1
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- WJCNZQLZVWNLKY-UHFFFAOYSA-N thiabendazole Chemical compound S1C=NC(C=2NC3=CC=CC=C3N=2)=C1 WJCNZQLZVWNLKY-UHFFFAOYSA-N 0.000 description 1
- 229960004546 thiabendazole Drugs 0.000 description 1
- NWWZPOKUUAIXIW-FLIBITNWSA-N thiamethoxam Chemical compound [O-][N+](=O)\N=C/1N(C)COCN\1CC1=CN=C(Cl)S1 NWWZPOKUUAIXIW-FLIBITNWSA-N 0.000 description 1
- BAKXBZPQTXCKRR-UHFFFAOYSA-N thiodicarb Chemical compound CSC(C)=NOC(=O)NSNC(=O)ON=C(C)SC BAKXBZPQTXCKRR-UHFFFAOYSA-N 0.000 description 1
- QGHREAKMXXNCOA-UHFFFAOYSA-N thiophanate-methyl Chemical compound COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC QGHREAKMXXNCOA-UHFFFAOYSA-N 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- OBZIQQJJIKNWNO-UHFFFAOYSA-N tolclofos-methyl Chemical compound COP(=S)(OC)OC1=C(Cl)C=C(C)C=C1Cl OBZIQQJJIKNWNO-UHFFFAOYSA-N 0.000 description 1
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical class CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 1
- 230000009261 transgenic effect Effects 0.000 description 1
- BAZVSMNPJJMILC-UHFFFAOYSA-N triadimenol Chemical compound C1=NC=NN1C(C(O)C(C)(C)C)OC1=CC=C(Cl)C=C1 BAZVSMNPJJMILC-UHFFFAOYSA-N 0.000 description 1
- IQGKIPDJXCAMSM-UHFFFAOYSA-N triazoxide Chemical compound N=1C2=CC=C(Cl)C=C2[N+]([O-])=NC=1N1C=CN=C1 IQGKIPDJXCAMSM-UHFFFAOYSA-N 0.000 description 1
- STCOOQWBFONSKY-UHFFFAOYSA-N tributyl phosphate Chemical compound CCCCOP(=O)(OCCCC)OCCCC STCOOQWBFONSKY-UHFFFAOYSA-N 0.000 description 1
- WVZPYZMQQDNINJ-UHFFFAOYSA-N tributyl(butylstannyloxy)stannane Chemical compound CCCC[SnH](CCCC)O[SnH](CCCC)CCCC WVZPYZMQQDNINJ-UHFFFAOYSA-N 0.000 description 1
- YDUBPEZBWPRJJL-UHFFFAOYSA-M tributyl-(4-chloro-2-phenylphenoxy)stannane Chemical compound CCCC[Sn](CCCC)(CCCC)OC1=CC=C(Cl)C=C1C1=CC=CC=C1 YDUBPEZBWPRJJL-UHFFFAOYSA-M 0.000 description 1
- HFFZSMFXOBHQLV-UHFFFAOYSA-M tributylstannyl dodecanoate Chemical compound CCCCCCCCCCCC(=O)O[Sn](CCCC)(CCCC)CCCC HFFZSMFXOBHQLV-UHFFFAOYSA-M 0.000 description 1
- PIILXFBHQILWPS-UHFFFAOYSA-N tributyltin Chemical compound CCCC[Sn](CCCC)CCCC PIILXFBHQILWPS-UHFFFAOYSA-N 0.000 description 1
- DQJCHOQLCLEDLL-UHFFFAOYSA-N tricyclazole Chemical compound CC1=CC=CC2=C1N1C=NN=C1S2 DQJCHOQLCLEDLL-UHFFFAOYSA-N 0.000 description 1
- HSMVPDGQOIQYSR-KGENOOAVSA-N triflumizole Chemical compound C1=CN=CN1C(/COCCC)=N/C1=CC=C(Cl)C=C1C(F)(F)F HSMVPDGQOIQYSR-KGENOOAVSA-N 0.000 description 1
- RROQIUMZODEXOR-UHFFFAOYSA-N triforine Chemical compound O=CNC(C(Cl)(Cl)Cl)N1CCN(C(NC=O)C(Cl)(Cl)Cl)CC1 RROQIUMZODEXOR-UHFFFAOYSA-N 0.000 description 1
- 229940036248 turpentine Drugs 0.000 description 1
- 238000009834 vaporization Methods 0.000 description 1
- 230000008016 vaporization Effects 0.000 description 1
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- 239000000080 wetting agent Substances 0.000 description 1
- 210000002268 wool Anatomy 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 239000005943 zeta-Cypermethrin Substances 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
- AMHNZOICSMBGDH-UHFFFAOYSA-L zineb Chemical compound [Zn+2].[S-]C(=S)NCCNC([S-])=S AMHNZOICSMBGDH-UHFFFAOYSA-L 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- 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
- A01N43/24—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 two or more hetero atoms
- A01N43/26—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 two or more hetero atoms five-membered rings
- A01N43/28—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 two or more hetero atoms five-membered rings with two hetero atoms in positions 1,3
-
- 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
- A01N51/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds having the sequences of atoms O—N—S, X—O—S, N—N—S, O—N—N or O-halogen, regardless of the number of bonds each atom has and with no atom of these sequences forming part of a heterocyclic 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
- A01N53/00—Biocides, pest repellants or attractants, or plant growth regulators containing cyclopropane carboxylic acids or derivatives thereof
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02A—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
- Y02A50/00—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
- Y02A50/30—Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change
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)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE10203688A DE10203688A1 (de) | 2002-01-31 | 2002-01-31 | Synergistische insektizide Mischungen |
PCT/EP2003/000478 WO2003063592A1 (de) | 2002-01-31 | 2003-01-20 | Synergistische insektizide mischungen |
Publications (1)
Publication Number | Publication Date |
---|---|
UA78280C2 true UA78280C2 (uk) | 2007-03-15 |
Family
ID=7713432
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
UA20040807169A UA78280C2 (uk) | 2002-01-31 | 2003-01-20 | Засіб для боротьби з шкідниками тварин |
Country Status (26)
Country | Link |
---|---|
US (2) | US7097848B2 (zh) |
EP (2) | EP1473997B1 (zh) |
KR (1) | KR100992946B1 (zh) |
CN (3) | CN1895048B (zh) |
AR (1) | AR038323A1 (zh) |
AT (1) | ATE550941T1 (zh) |
AU (2) | AU2003202575B2 (zh) |
BR (2) | BR122013019371B1 (zh) |
CA (1) | CA2474086C (zh) |
CO (1) | CO5600986A2 (zh) |
DE (1) | DE10203688A1 (zh) |
DK (1) | DK1473997T3 (zh) |
EG (1) | EG23409A (zh) |
ES (2) | ES2400288T3 (zh) |
HR (1) | HRP20040789B1 (zh) |
IL (1) | IL163106A (zh) |
ME (1) | MEP11008A (zh) |
MX (1) | MXPA04007298A (zh) |
NZ (1) | NZ534368A (zh) |
PL (2) | PL212915B1 (zh) |
PT (1) | PT1473997E (zh) |
RS (1) | RS52708B (zh) |
SI (2) | SI1473997T1 (zh) |
UA (1) | UA78280C2 (zh) |
WO (1) | WO2003063592A1 (zh) |
ZA (1) | ZA200405968B (zh) |
Families Citing this family (41)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1297545C (zh) * | 1998-06-10 | 2007-01-31 | 拜尔公司 | 防治植物有害生物的组合物 |
DE10347440A1 (de) * | 2003-10-13 | 2005-05-04 | Bayer Cropscience Ag | Synergistische insektizide Mischungen |
EP1922930A3 (en) * | 2004-03-16 | 2013-02-20 | Syngenta Participations AG | Pesticidal composition and method for seed treatment |
AU2005231132B2 (en) * | 2004-03-25 | 2011-06-09 | Fmc Corporation | Liquid termiticide compositions of pyrethroids and a neonicitinoids |
DE102004032418A1 (de) * | 2004-04-07 | 2005-10-27 | Bayer Cropscience Ag | Wirkstoffkombinationen mit insektiziden Eigenschaften |
DE102004033289A1 (de) * | 2004-04-24 | 2005-11-10 | Bayer Cropscience Ag | Synergistische insektizide Mischungen |
DE102004062512A1 (de) * | 2004-12-24 | 2006-07-06 | Bayer Cropscience Ag | Synergistische Mischungen mit insektizider und fungizider Wirkung |
JP2006219463A (ja) * | 2005-02-14 | 2006-08-24 | Chemiprokasei Kaisha Ltd | 木材害虫防除組成物 |
BRPI0607259A2 (pt) * | 2005-02-24 | 2009-08-25 | Syngenta Participations Ag | método para melhorar o crescimento de plantas resistentes ou tolerantes a nematóides |
AR056290A1 (es) | 2005-03-31 | 2007-10-03 | Nippon Soda Co | Metodo para inhibir la produccion de de micotoxina |
EP1865771A1 (en) * | 2005-04-08 | 2007-12-19 | Syngeta Participations AG | Method of mollusc control |
US20070099963A1 (en) * | 2005-11-01 | 2007-05-03 | Bayer Cropscience Lp | Nematicidal compositions and methods |
DE102006014487A1 (de) * | 2006-03-29 | 2007-10-04 | Bayer Cropscience Ag | Wirkstoffkombinationen mit insektiziden Eigenschaften |
TR200901842T1 (tr) * | 2006-09-12 | 2009-06-22 | Nippon Soda Co., Ltd. | Stabil süspansiyon formunda haşere kontrol ajanı |
WO2010092031A2 (en) * | 2009-02-11 | 2010-08-19 | Basf Se | Pesticidal mixtures |
WO2010092028A2 (en) * | 2009-02-11 | 2010-08-19 | Basf Se | Pesticidal mixtures |
CN102232385A (zh) * | 2010-04-25 | 2011-11-09 | 青岛凯源祥化工有限公司 | 一种含有噻虫胺和阿维菌素的杀虫组合物 |
NZ603839A (en) | 2010-04-27 | 2014-12-24 | Sumitomo Chemical Co | Pesticidal composition and its use |
JP5712504B2 (ja) | 2010-04-27 | 2015-05-07 | 住友化学株式会社 | 有害生物防除組成物およびその用途 |
CA2797376C (en) | 2010-04-28 | 2018-11-20 | Sumitomo Chemical Company, Limited | Plant disease controlling compositions comprising a carboxamide compound and an azole fungicide |
NZ603844A (en) | 2010-04-28 | 2014-08-29 | Sumitomo Chemical Co | Pesticidal composition and its use |
JP5724211B2 (ja) | 2010-04-28 | 2015-05-27 | 住友化学株式会社 | 植物病害防除組成物およびその用途 |
WO2012124795A1 (en) * | 2011-03-17 | 2012-09-20 | Sumitomo Chemical Company, Limited | Pest control composition and pest control method |
CN102379308A (zh) * | 2011-09-21 | 2012-03-21 | 江苏扬农化工股份有限公司 | 含有噻虫胺的复配杀虫组合物及其应用 |
CN102365970A (zh) * | 2011-09-30 | 2012-03-07 | 山东京蓬生物药业股份有限公司 | 含有噻虫胺和甲氨基阿维菌素苯甲酸盐的增效杀虫组合物及其应用 |
CN102428951A (zh) * | 2012-01-14 | 2012-05-02 | 陕西美邦农药有限公司 | 一种含有噻虫胺的杀虫组合物 |
EP2811834A1 (en) * | 2012-02-08 | 2014-12-17 | Bayer Intellectual Property GmbH | Active compound compositions for vector control of insecticide-resistant pests |
CN102763672B (zh) * | 2012-08-13 | 2014-01-08 | 广西汇丰生物科技有限公司 | 含伊维菌素和噻虫胺的颗粒剂 |
CN103621537A (zh) * | 2012-08-29 | 2014-03-12 | 南京华洲药业有限公司 | 一种含噻虫胺和甲维盐的增效杀虫组合物及其应用 |
EA030236B1 (ru) * | 2012-11-30 | 2018-07-31 | Байер Кропсайенс Акциенгезельшафт | Тройные фунгицидные и пестицидные смеси |
CN103798275A (zh) * | 2014-02-21 | 2014-05-21 | 罗晓丹 | 一种防治甘蔗地下害虫的农药颗粒剂 |
CN103875704A (zh) * | 2014-03-19 | 2014-06-25 | 黄业新 | 一种含噻虫胺和二嗪磷的农药颗粒剂 |
CN105432666B (zh) * | 2015-11-19 | 2018-07-31 | 广州万粤知识产权运营有限公司 | 一种含苏云金杆菌的农药组合物 |
CN106386842A (zh) * | 2016-08-17 | 2017-02-15 | 陕西西大华特科技实业有限公司 | 一种含有噻虫胺和高效氯氟氰菊酯的杀虫组合物 |
CN106508948B (zh) * | 2016-10-27 | 2019-03-26 | 山东润博生物科技有限公司 | 一种含有阿维菌素和噻虫胺的悬浮种衣剂及其应用 |
CN107156168A (zh) * | 2017-06-21 | 2017-09-15 | 天峨县平昌生态农业有限公司 | 一种用于防治小菜蛾的杀虫组合物 |
CN109907073B (zh) * | 2018-11-06 | 2024-02-23 | 宁夏大学 | 一种防治粉虱的生物农药以及用途 |
CN111011368A (zh) * | 2019-11-11 | 2020-04-17 | 南京华洲药业有限公司 | 含高效氯氟氰菊酯和甲氨基阿维菌素苯甲酸盐的复合杀虫杀螨纳米水剂及其用途 |
CN111084191B (zh) * | 2019-12-25 | 2022-02-25 | 南京保丰农药有限公司 | 噻虫胺和高效氟氯氰菊酯悬浮剂及其制备方法 |
CN112956480A (zh) * | 2021-02-04 | 2021-06-15 | 四川眉山凯尔化工有限公司 | 一种农药杀虫剂原药配方 |
CN117598324A (zh) * | 2023-11-21 | 2024-02-27 | 西南大学 | 一种基于球孢白僵菌的防治橘小实蝇药剂及其测试方法 |
Family Cites Families (25)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3313684A (en) | 1959-12-05 | 1967-04-11 | Bayer Ag | 3, 5-dimethyl-4-methylmercaptophenyl n-methyl carbamate and methods for combating insects |
SE434277B (sv) | 1976-04-19 | 1984-07-16 | Merck & Co Inc | Sett att framstella nya antihelmintiskt verkande foreningar genom odling av streptomyces avermitilis |
US4427663A (en) | 1982-03-16 | 1984-01-24 | Merck & Co., Inc. | 4"-Keto-and 4"-amino-4"-deoxy avermectin compounds and substituted amino derivatives thereof |
ZA836964B (en) | 1982-10-11 | 1984-05-30 | Ici Plc | Insecticidal product and preparation thereof |
GB8308507D0 (en) | 1983-03-28 | 1983-05-05 | Ici Plc | Insecticidal product |
GB2130199A (en) | 1982-10-11 | 1984-05-31 | Ici Plc | An enantiomeric pair of cyhalothrin isomers and process for the preparation thereof |
DE3522629A1 (de) | 1985-06-25 | 1987-01-08 | Bayer Ag | Verfahren zur herstellung bestimmter enantiomerenpaare von permethrinsaeure-(alpha)-cyano-3-phenoxy-4-fluor-benzyl -ester |
US4874749A (en) | 1987-07-31 | 1989-10-17 | Merck & Co., Inc. | 4"-Deoxy-4-N-methylamino avermectin Bla/Blb |
JP2779403B2 (ja) | 1988-11-29 | 1998-07-23 | 日本バイエルアグロケム株式会社 | 殺虫性ニトロ化合物 |
US5238949A (en) | 1988-11-29 | 1993-08-24 | Nihon Bayer Agrochem K.K. | Insecticidally active nitro pyridyl compounds |
IE71183B1 (en) | 1988-12-27 | 1997-01-29 | Takeda Chemical Industries Ltd | Guanidine derivatives their production and insecticides |
ES2059841T3 (es) | 1989-02-13 | 1994-11-16 | Bayer Agrochem Kk | Nitro compuestos con actividad insecticida. |
US5204359A (en) | 1989-02-13 | 1993-04-20 | Nihon Bayer Agrochem K.K. | Insecticidally active nitro compounds |
US4874794A (en) | 1989-04-28 | 1989-10-17 | Lidak Biopharmaceuticals | Inflammatory disease treatment |
IL98599A (en) | 1990-06-28 | 1995-06-29 | Merck & Co Inc | Stable salts of "4-deoxy-" 4-epi-methylamino abramectin and insecticides containing them |
US6828275B2 (en) * | 1998-06-23 | 2004-12-07 | Bayer Aktiengesellschaft | Synergistic insecticide mixtures |
DE19823396A1 (de) * | 1998-05-26 | 1999-12-02 | Bayer Ag | Synergistische insektizide Mischungen |
PL197431B1 (pl) * | 1998-07-02 | 2008-03-31 | Lilly Co Eli | Szampon do zwalczania wszawicy u ludzi, preparat przeciw wszawicy kondycjonujący włosy, płukanka przeciw wszawicy, zastosowanie spinozyny lub jej pochodnej lub soli do wytwarzania leku do leczenia wszawicy |
ATE289750T1 (de) | 1998-11-20 | 2005-03-15 | Bayer Cropscience Ag | Fungizide wirkstoffkombinationen |
US6586617B1 (en) * | 1999-04-28 | 2003-07-01 | Sumitomo Chemical Takeda Agro Company, Limited | Sulfonamide derivatives |
US6927210B1 (en) * | 1999-08-12 | 2005-08-09 | Eli Lilly And Company | Ectoparasiticidal aqueous suspension formulations of spinosyns |
MY138097A (en) * | 2000-03-22 | 2009-04-30 | Du Pont | Insecticidal anthranilamides |
JP4324308B2 (ja) * | 2000-04-26 | 2009-09-02 | 住友化学株式会社 | ハエ類の防除方法 |
US6838473B2 (en) * | 2000-10-06 | 2005-01-04 | Monsanto Technology Llc | Seed treatment with combinations of pyrethrins/pyrethroids and clothiandin |
US6660690B2 (en) * | 2000-10-06 | 2003-12-09 | Monsanto Technology, L.L.C. | Seed treatment with combinations of insecticides |
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- 2003-01-20 BR BRBR122013019371-5A patent/BR122013019371B1/pt active IP Right Grant
- 2003-01-20 BR BRPI0307356-4A patent/BR0307356B1/pt active IP Right Grant
- 2003-01-20 ME MEP-110/08A patent/MEP11008A/xx unknown
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