AP221A - Fungicidal compositions for seed dressing. - Google Patents
Fungicidal compositions for seed dressing. Download PDFInfo
- Publication number
- AP221A AP221A APAP/P/1991/000277A AP9100277A AP221A AP 221 A AP221 A AP 221A AP 9100277 A AP9100277 A AP 9100277A AP 221 A AP221 A AP 221A
- Authority
- AP
- ARIPO
- Prior art keywords
- fungicide
- seed
- plant propagation
- propagation product
- protection
- Prior art date
Links
- 230000000855 fungicidal effect Effects 0.000 title claims description 59
- 239000000203 mixture Substances 0.000 title claims description 50
- 208000031888 Mycoses Diseases 0.000 claims abstract description 5
- 239000000417 fungicide Substances 0.000 claims description 62
- 241000196324 Embryophyta Species 0.000 claims description 42
- 238000000034 method Methods 0.000 claims description 27
- 239000013543 active substance Substances 0.000 claims description 13
- 235000013339 cereals Nutrition 0.000 claims description 8
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 claims description 6
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- KUAZQDVKQLNFPE-UHFFFAOYSA-N thiram Chemical compound CN(C)C(=S)SSC(=S)N(C)C KUAZQDVKQLNFPE-UHFFFAOYSA-N 0.000 claims description 6
- 229960002447 thiram Drugs 0.000 claims description 6
- 239000005745 Captan Substances 0.000 claims description 5
- 240000007594 Oryza sativa Species 0.000 claims description 5
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- 239000005843 Thiram Substances 0.000 claims description 5
- 240000008042 Zea mays Species 0.000 claims description 5
- 235000016383 Zea mays subsp huehuetenangensis Nutrition 0.000 claims description 5
- 235000002017 Zea mays subsp mays Nutrition 0.000 claims description 5
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- 235000009973 maize Nutrition 0.000 claims description 5
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- 235000009566 rice Nutrition 0.000 claims description 5
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- ZQPPMHVWECSIRJ-KTKRTIGZSA-M oleate Chemical compound CCCCCCCC\C=C/CCCCCCCC([O-])=O ZQPPMHVWECSIRJ-KTKRTIGZSA-M 0.000 description 1
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- QXJKBPAVAHBARF-UHFFFAOYSA-N procymidone Chemical compound O=C1C2(C)CC2(C)C(=O)N1C1=CC(Cl)=CC(Cl)=C1 QXJKBPAVAHBARF-UHFFFAOYSA-N 0.000 description 1
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- 150000003230 pyrimidines Chemical class 0.000 description 1
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- XOAAWQZATWQOTB-UHFFFAOYSA-N taurine Chemical class NCCS(O)(=O)=O XOAAWQZATWQOTB-UHFFFAOYSA-N 0.000 description 1
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- BAKXBZPQTXCKRR-UHFFFAOYSA-N thiodicarb Chemical compound CSC(C)=NOC(=O)NSNC(=O)ON=C(C)SC BAKXBZPQTXCKRR-UHFFFAOYSA-N 0.000 description 1
- 238000002054 transplantation Methods 0.000 description 1
- VFJYIHQDILEQNR-UHFFFAOYSA-M trimethylsulfanium;iodide Chemical compound [I-].C[S+](C)C VFJYIHQDILEQNR-UHFFFAOYSA-M 0.000 description 1
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Classifications
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01C—PLANTING; SOWING; FERTILISING
- A01C1/00—Apparatus, or methods of use thereof, for testing or treating seed, roots, or the like, prior to sowing or planting
- A01C1/06—Coating or dressing seed
-
- 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
- A01N43/64—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with three nitrogen atoms as the only ring hetero atoms
- A01N43/647—Triazoles; Hydrogenated triazoles
- A01N43/653—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Environmental Sciences (AREA)
- Health & Medical Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Soil Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR9007607A FR2663196A1 (fr) | 1990-06-13 | 1990-06-13 | Composition fongicide a base d'un triazole et d'une autre matiere active pour le traitement des semences. |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| AP9100277A0 AP9100277A0 (en) | 1991-07-31 |
| AP221A true AP221A (en) | 1992-10-21 |
Family
ID=9397742
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| APAP/P/1991/000277A AP221A (en) | 1990-06-13 | 1991-06-12 | Fungicidal compositions for seed dressing. |
Country Status (30)
| Country | Link |
|---|---|
| US (2) | US5290791A (cs) |
| EP (1) | EP0467792B1 (cs) |
| JP (1) | JPH04230204A (cs) |
| KR (1) | KR920000230A (cs) |
| CN (1) | CN1063396A (cs) |
| AP (1) | AP221A (cs) |
| AT (1) | ATE122205T1 (cs) |
| AU (1) | AU656320B2 (cs) |
| BR (1) | BR9102433A (cs) |
| CA (1) | CA2043812A1 (cs) |
| CS (1) | CS178491A3 (cs) |
| DE (1) | DE69109560T2 (cs) |
| DK (1) | DK0467792T3 (cs) |
| EG (1) | EG19259A (cs) |
| ES (1) | ES2071958T3 (cs) |
| FI (1) | FI97195C (cs) |
| FR (1) | FR2663196A1 (cs) |
| HU (1) | HU209725B (cs) |
| IE (1) | IE67894B1 (cs) |
| IL (1) | IL98400A (cs) |
| MA (1) | MA22180A1 (cs) |
| MY (1) | MY106539A (cs) |
| NO (1) | NO912238L (cs) |
| OA (1) | OA09364A (cs) |
| PL (1) | PL290663A1 (cs) |
| PT (1) | PT97934B (cs) |
| RO (1) | RO111980B1 (cs) |
| RU (1) | RU2035140C1 (cs) |
| TR (1) | TR25435A (cs) |
| ZA (1) | ZA914529B (cs) |
Families Citing this family (37)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2663195A1 (fr) * | 1990-06-13 | 1991-12-20 | Rhone Poulenc Agrochimie | Procede de traitement fongicide foliaire au moyen d'un triazole et composition fongicide pour mettre en óoeuvre le procede. |
| DE4122868A1 (de) * | 1991-07-11 | 1993-01-14 | Bayer Ag | Mikrobizide wirkstoffkombinationen |
| FR2708415B1 (fr) * | 1993-06-23 | 1996-08-30 | Rhone Poulenc Agrochimie | Traitement de semences à l'aide d'acide phosphoreux ou un de ses sels, et semences ainsi traitées. |
| FR2706736B1 (cs) * | 1993-06-23 | 1995-08-25 | Rhone Poulenc Agrochimie | |
| FR2712144B1 (fr) * | 1993-11-04 | 1997-07-18 | Rhone Poulenc Agrochimie | Association d'un fongicide à groupe azole avec un insecticide à groupe pyrazole, pyrrole ou phénylimidazole. |
| FR2711893B1 (fr) * | 1993-11-04 | 1996-01-12 | Rhone Poulenc Agrochimie | Association d'un fongicide à groupe azole avec un insecticide à groupe pyrazole, pyrrole ou phénylimidazole. |
| US5506250A (en) * | 1994-11-14 | 1996-04-09 | Rhone-Poulenc Inc. | Method of treating turf |
| DE19523449A1 (de) * | 1995-06-28 | 1997-01-02 | Bayer Ag | Verfahren zur Herstellung von 2,2-Dialkyl-aryliden-cycloalkanonen |
| FR2742311B1 (fr) * | 1995-12-19 | 1998-01-16 | Rhone Poulenc Agrochimie | Compositions fongicides synergiques a base de triticonazole |
| FR2742310B1 (fr) * | 1995-12-19 | 1998-01-16 | Rhone Poulenc Agrochimie | Nouvelle composition fongicide a base de triticonazole et de pyrimethanil |
| US5736164A (en) * | 1996-08-30 | 1998-04-07 | Taylor; John B. | Fungicidal compositions for plants containing phosphonate and phosphate salts, and derivatives thereof |
| US5800837A (en) * | 1996-08-30 | 1998-09-01 | Foliar Nutrients, Inc. | Plant fertilizer compositions containing phosphonate and phosphate salts and derivatives thereof |
| US6338860B1 (en) | 1996-08-30 | 2002-01-15 | Foliar Nutrients, Inc. | Compositions for plants containing phosphonate and phosphate salts, and derivatives thereof |
| RU2202185C2 (ru) * | 1997-06-16 | 2003-04-20 | Новартис Аг | Композиция, обладающая синергетической активностью в отношении поражения растений болезнями, и способ защиты растений от фитопатогенных болезней |
| KR100587198B1 (ko) * | 1997-08-28 | 2006-10-19 | 신젠타 파티서페이션즈 아게 | 곤충 또는 대표적 진드기 목의 방제용 물질 |
| CN1088330C (zh) * | 1999-08-11 | 2002-07-31 | 桂保华 | 种子处理剂 |
| JP2002291340A (ja) * | 2001-04-02 | 2002-10-08 | Dainichiseika Color & Chem Mfg Co Ltd | セル苗処理剤、セル苗処理方法及びセル苗の定植方法 |
| AU2003289183B2 (en) * | 2002-12-04 | 2009-09-10 | Hokkai Sankyo Co., Ltd. | Method of preventing wheat from mycotoxin contamination |
| US6743752B2 (en) | 2003-03-28 | 2004-06-01 | Northern Quinoa Corporation | Method of protecting plants from bacterial diseases |
| US20050261129A1 (en) * | 2003-09-22 | 2005-11-24 | Dutcheshen Joseph M | Method of protecting plants from bacterial and fungal diseases |
| UA66740A (en) * | 2003-12-31 | 2004-05-17 | Prezens Ltd Liability Company | Pesticidal composition |
| EP1550371A3 (en) * | 2003-12-31 | 2006-08-16 | Tovarystvo z obmegenoyu vidpovidalnistyu "Prezence" | Pesticidal compositions comprising an oxathiin and triazole fungicides |
| BRPI0615849B1 (pt) * | 2005-09-13 | 2015-12-01 | Basf Se | método de proteção de uma planta contra um fitopatógeno, uso de um composto, e, composição para tratar semente de uma planta para protegê-la contra um fitopatógeno |
| CN101583279A (zh) * | 2007-01-17 | 2009-11-18 | 巴斯夫欧洲公司 | 保护植物以防腐霉属和丝核菌属的方法、用途和试剂 |
| WO2008135480A2 (en) * | 2007-05-02 | 2008-11-13 | Basf Se | Method for controlling specific fungal pathogen in soybeans by employing benodanil |
| MX2013003584A (es) * | 2010-10-01 | 2013-09-06 | Basf Se | Proceso para preparar 5-[1-(4-clorofenil)-metilen]-1-hidroximetil- 2, 2-dimetil-ciclopentanol. |
| CN102150672B (zh) * | 2010-12-16 | 2013-04-10 | 陕西韦尔奇作物保护有限公司 | 一种含有克菌丹与三唑类化合物的杀菌组合物 |
| CN102150667A (zh) * | 2011-02-26 | 2011-08-17 | 陕西美邦农药有限公司 | 一种含有十三吗啉的增效杀菌组合物 |
| CN102204540B (zh) * | 2011-04-02 | 2014-03-05 | 陕西汤普森生物科技有限公司 | 一种含有乙嘧酚与三唑类化合物的杀菌组合物 |
| CN102217605A (zh) * | 2011-04-20 | 2011-10-19 | 陕西汤普森生物科技有限公司 | 一种含氟酰胺与三唑类化合物的杀菌组合物 |
| AU2012257748B2 (en) * | 2011-05-17 | 2016-06-30 | Bayer Intellectual Property Gmbh | Active compound combinations |
| WO2013117629A1 (en) | 2012-02-10 | 2013-08-15 | Basf Agro B.V., Arnhem (Nl), Zürich-Branch | Process for preparing cis-5-[1-(4-chlorophenyl)-methylene]-1-hydroxymethyl-2,2-dimethylcyclopentanol |
| FR3088804B1 (fr) * | 2018-11-22 | 2020-11-27 | Limagrain Europe | Composition antifongique pour pelliculage de semences |
| CN110204500A (zh) * | 2019-07-17 | 2019-09-06 | 九江德思光电材料有限公司 | 一种叶菌唑的制备方法 |
| CN110305077A (zh) * | 2019-07-17 | 2019-10-08 | 九江德思光电材料有限公司 | 一种叶菌唑环氧化中间体的合成方法 |
| RU2723184C1 (ru) * | 2019-08-14 | 2020-06-09 | Оганесов Армен Владимирович | Фунгицид и способ его производства |
| EP4140305A4 (en) * | 2020-12-18 | 2024-08-14 | University of Hyogo | SEED GERMINATION PROMOTION LIQUID AND METHOD FOR PROMOTING SEED GERMINATION THEREOF |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2641277A1 (fr) * | 1988-12-29 | 1990-07-06 | Rhone Poulenc Agrochimie | Azolylmethylcyclopentane ou cyclopentene benzolidene et utilisation comme fongicide |
| EP0378953A1 (fr) * | 1988-12-29 | 1990-07-25 | Rhone-Poulenc Agrochimie | Benzylidène azolylméthylecycloalcane et utilisation comme fongicide |
| DE3941593A1 (de) * | 1989-12-16 | 1991-06-20 | Basf Ag | Azolylmethylcycloalkanole |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR378953A (fr) * | 1907-06-18 | 1907-10-22 | Fulton Co | Régulateur automatique de température pour installations de chauffage et autres applications |
| US3823240A (en) * | 1970-10-06 | 1974-07-09 | Rhone Poulenc Sa | Fungicidal hydantoin derivatives |
| EP0052424B2 (en) * | 1980-11-19 | 1990-02-28 | Imperial Chemical Industries Plc | Triazole compounds, a process for preparing them, their use as plant fungicides and fungicidal compositions containing them |
| DE3333411A1 (de) * | 1983-09-16 | 1985-04-04 | Bayer Ag, 5090 Leverkusen | Fungizide mittel |
| IT1196465B (it) * | 1986-07-07 | 1988-11-16 | Montedison Spa | Miscele fungicide |
| JPH0625140B2 (ja) * | 1986-11-10 | 1994-04-06 | 呉羽化学工業株式会社 | 新規アゾール誘導体、その製造方法及び該誘導体の農園芸用薬剤 |
| US4940722A (en) * | 1986-12-10 | 1990-07-10 | Sumitomo Chemical Companmy, Limited | Seed disinfectant composition |
| US5256683A (en) * | 1988-12-29 | 1993-10-26 | Rhone-Poulenc Agrochimie | Fungicidal compositions containing (benzylidene)-azolylmethylcycloalkane |
| FR2663195A1 (fr) * | 1990-06-13 | 1991-12-20 | Rhone Poulenc Agrochimie | Procede de traitement fongicide foliaire au moyen d'un triazole et composition fongicide pour mettre en óoeuvre le procede. |
-
1990
- 1990-06-13 FR FR9007607A patent/FR2663196A1/fr not_active Withdrawn
-
1991
- 1991-06-04 CA CA002043812A patent/CA2043812A1/en not_active Abandoned
- 1991-06-06 IL IL98400A patent/IL98400A/en not_active IP Right Cessation
- 1991-06-11 AT AT91420188T patent/ATE122205T1/de not_active IP Right Cessation
- 1991-06-11 DK DK91420188.4T patent/DK0467792T3/da active
- 1991-06-11 NO NO91912238A patent/NO912238L/no unknown
- 1991-06-11 ES ES91420188T patent/ES2071958T3/es not_active Expired - Lifetime
- 1991-06-11 EP EP91420188A patent/EP0467792B1/fr not_active Expired - Lifetime
- 1991-06-11 PT PT97934A patent/PT97934B/pt not_active IP Right Cessation
- 1991-06-11 EG EG36091A patent/EG19259A/xx active
- 1991-06-11 DE DE69109560T patent/DE69109560T2/de not_active Expired - Fee Related
- 1991-06-11 MA MA22455A patent/MA22180A1/fr unknown
- 1991-06-11 CS CS911784A patent/CS178491A3/cs unknown
- 1991-06-12 AP APAP/P/1991/000277A patent/AP221A/en active
- 1991-06-12 HU HU911959A patent/HU209725B/hu not_active IP Right Cessation
- 1991-06-12 RU SU914895734A patent/RU2035140C1/ru active
- 1991-06-12 RO RO147775A patent/RO111980B1/ro unknown
- 1991-06-12 AU AU78340/91A patent/AU656320B2/en not_active Ceased
- 1991-06-12 IE IE199291A patent/IE67894B1/en not_active IP Right Cessation
- 1991-06-12 BR BR919102433A patent/BR9102433A/pt not_active Application Discontinuation
- 1991-06-12 MY MYPI91001046A patent/MY106539A/en unknown
- 1991-06-12 FI FI912822A patent/FI97195C/fi not_active IP Right Cessation
- 1991-06-13 KR KR1019910009753A patent/KR920000230A/ko not_active Withdrawn
- 1991-06-13 OA OA60018A patent/OA09364A/xx unknown
- 1991-06-13 CN CN91104062A patent/CN1063396A/zh active Pending
- 1991-06-13 ZA ZA914529A patent/ZA914529B/xx unknown
- 1991-06-13 PL PL29066391A patent/PL290663A1/xx unknown
- 1991-06-13 JP JP3142059A patent/JPH04230204A/ja active Pending
- 1991-06-13 US US07/714,726 patent/US5290791A/en not_active Expired - Fee Related
- 1991-06-13 TR TR91/0599A patent/TR25435A/xx unknown
-
1993
- 1993-12-03 US US08/162,494 patent/US5629330A/en not_active Expired - Fee Related
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2641277A1 (fr) * | 1988-12-29 | 1990-07-06 | Rhone Poulenc Agrochimie | Azolylmethylcyclopentane ou cyclopentene benzolidene et utilisation comme fongicide |
| EP0378953A1 (fr) * | 1988-12-29 | 1990-07-25 | Rhone-Poulenc Agrochimie | Benzylidène azolylméthylecycloalcane et utilisation comme fongicide |
| DE3941593A1 (de) * | 1989-12-16 | 1991-06-20 | Basf Ag | Azolylmethylcycloalkanole |
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