UA62978C2 - Synergistic compositions comprising imazalil and epoxiconazole - Google Patents
Synergistic compositions comprising imazalil and epoxiconazole Download PDFInfo
- Publication number
- UA62978C2 UA62978C2 UA2000021178A UA2000021178A UA62978C2 UA 62978 C2 UA62978 C2 UA 62978C2 UA 2000021178 A UA2000021178 A UA 2000021178A UA 2000021178 A UA2000021178 A UA 2000021178A UA 62978 C2 UA62978 C2 UA 62978C2
- Authority
- UA
- Ukraine
- Prior art keywords
- imazalil
- active ingredients
- composition according
- composition
- plants
- Prior art date
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- 239000000203 mixture Substances 0.000 title claims abstract description 76
- PZBPKYOVPCNPJY-UHFFFAOYSA-N 1-[2-(allyloxy)-2-(2,4-dichlorophenyl)ethyl]imidazole Chemical compound ClC1=CC(Cl)=CC=C1C(OCC=C)CN1C=NC=C1 PZBPKYOVPCNPJY-UHFFFAOYSA-N 0.000 title claims abstract description 42
- 229960002125 enilconazole Drugs 0.000 title claims abstract description 29
- 239000005795 Imazalil Substances 0.000 title claims abstract description 28
- 239000005767 Epoxiconazole Substances 0.000 title claims abstract description 11
- 230000002195 synergetic effect Effects 0.000 title claims abstract description 11
- ZMYFCFLJBGAQRS-IRXDYDNUSA-N (2R,3S)-epoxiconazole Chemical compound C1=CC(F)=CC=C1[C@@]1(CN2N=CN=C2)[C@H](C=2C(=CC=CC=2)Cl)O1 ZMYFCFLJBGAQRS-IRXDYDNUSA-N 0.000 title abstract 2
- 150000003839 salts Chemical class 0.000 claims abstract description 23
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- 239000004480 active ingredient Substances 0.000 claims description 35
- ZMYFCFLJBGAQRS-IAGOWNOFSA-N (2S,3R)-epoxiconazole Chemical compound C1=CC(F)=CC=C1[C@]1(CN2N=CN=C2)[C@@H](C=2C(=CC=CC=2)Cl)O1 ZMYFCFLJBGAQRS-IAGOWNOFSA-N 0.000 claims description 17
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- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- FITIWKDOCAUBQD-UHFFFAOYSA-N prothiofos Chemical compound CCCSP(=S)(OCC)OC1=CC=C(Cl)C=C1Cl FITIWKDOCAUBQD-UHFFFAOYSA-N 0.000 description 1
- 239000008262 pumice Substances 0.000 description 1
- 229940015367 pyrethrum Drugs 0.000 description 1
- 125000001453 quaternary ammonium group Chemical group 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 235000021013 raspberries Nutrition 0.000 description 1
- 229940108410 resmethrin Drugs 0.000 description 1
- VEMKTZHHVJILDY-FIWHBWSRSA-N resmethrin Chemical compound CC1(C)[C@H](C=C(C)C)C1C(=O)OCC1=COC(CC=2C=CC=CC=2)=C1 VEMKTZHHVJILDY-FIWHBWSRSA-N 0.000 description 1
- 230000004044 response Effects 0.000 description 1
- 235000009566 rice Nutrition 0.000 description 1
- 229940080817 rotenone Drugs 0.000 description 1
- JUVIOZPCNVVQFO-UHFFFAOYSA-N rotenone Natural products O1C2=C3CC(C(C)=C)OC3=CC=C2C(=O)C2C1COC1=C2C=C(OC)C(OC)=C1 JUVIOZPCNVVQFO-UHFFFAOYSA-N 0.000 description 1
- 150000003873 salicylate salts Chemical class 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 235000003441 saturated fatty acids Nutrition 0.000 description 1
- 239000000565 sealant Substances 0.000 description 1
- 229910052624 sepiolite Inorganic materials 0.000 description 1
- 235000019355 sepiolite Nutrition 0.000 description 1
- HPYNBECUCCGGPA-UHFFFAOYSA-N silafluofen Chemical compound C1=CC(OCC)=CC=C1[Si](C)(C)CCCC1=CC=C(F)C(OC=2C=CC=CC=2)=C1 HPYNBECUCCGGPA-UHFFFAOYSA-N 0.000 description 1
- 150000004756 silanes Chemical class 0.000 description 1
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 235000019337 sorbitan trioleate Nutrition 0.000 description 1
- 229960000391 sorbitan trioleate Drugs 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- SFVFIFLLYFPGHH-UHFFFAOYSA-M stearalkonium chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCCCC[N+](C)(C)CC1=CC=CC=C1 SFVFIFLLYFPGHH-UHFFFAOYSA-M 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 238000004659 sterilization and disinfection Methods 0.000 description 1
- 235000021012 strawberries Nutrition 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 150000003459 sulfonic acid esters Chemical class 0.000 description 1
- 125000000542 sulfonic acid group Chemical group 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 150000003892 tartrate salts Chemical class 0.000 description 1
- 235000013616 tea Nutrition 0.000 description 1
- 239000012085 test solution Substances 0.000 description 1
- 230000001225 therapeutic effect Effects 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
- 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
- 229940024986 topical antifungal imidazole and triazole derivative Drugs 0.000 description 1
- YWSCPYYRJXKUDB-KAKFPZCNSA-N tralomethrin Chemical compound CC1(C)[C@@H](C(Br)C(Br)(Br)Br)[C@H]1C(=O)O[C@H](C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 YWSCPYYRJXKUDB-KAKFPZCNSA-N 0.000 description 1
- KVSKGMLNBAPGKH-UHFFFAOYSA-N tribromosalicylanilide Chemical compound OC1=C(Br)C=C(Br)C=C1C(=O)NC1=CC=C(Br)C=C1 KVSKGMLNBAPGKH-UHFFFAOYSA-N 0.000 description 1
- PIILXFBHQILWPS-UHFFFAOYSA-N tributyltin Chemical class CCCC[Sn](CCCC)CCCC PIILXFBHQILWPS-UHFFFAOYSA-N 0.000 description 1
- NFACJZMKEDPNKN-UHFFFAOYSA-N trichlorfon Chemical compound COP(=O)(OC)C(O)C(Cl)(Cl)Cl NFACJZMKEDPNKN-UHFFFAOYSA-N 0.000 description 1
- YNJBWRMUSHSURL-UHFFFAOYSA-N trichloroacetic acid Chemical class OC(=O)C(Cl)(Cl)Cl YNJBWRMUSHSURL-UHFFFAOYSA-N 0.000 description 1
- ICUTUKXCWQYESQ-UHFFFAOYSA-N triclocarban Chemical compound C1=CC(Cl)=CC=C1NC(=O)NC1=CC=C(Cl)C(Cl)=C1 ICUTUKXCWQYESQ-UHFFFAOYSA-N 0.000 description 1
- 229960001325 triclocarban Drugs 0.000 description 1
- GWBUNZLLLLDXMD-UHFFFAOYSA-H tricopper;dicarbonate;dihydroxide Chemical compound [OH-].[OH-].[Cu+2].[Cu+2].[Cu+2].[O-]C([O-])=O.[O-]C([O-])=O GWBUNZLLLLDXMD-UHFFFAOYSA-H 0.000 description 1
- HVLUSYMLLVVXGI-USGGBSEESA-M trimethyl-[(z)-octadec-9-enyl]azanium;chloride Chemical compound [Cl-].CCCCCCCC\C=C/CCCCCCCC[N+](C)(C)C HVLUSYMLLVVXGI-USGGBSEESA-M 0.000 description 1
- 235000021122 unsaturated fatty acids Nutrition 0.000 description 1
- 150000003672 ureas Chemical class 0.000 description 1
- 150000003751 zinc Chemical class 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 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
- A01N43/64—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)
- 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)
- Pretreatment Of Seeds And Plants (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP97202760 | 1997-09-08 | ||
PCT/EP1998/005711 WO1999012422A1 (en) | 1997-09-08 | 1998-09-01 | Synergistic compositions comprising imazalil and epoxiconazole |
Publications (1)
Publication Number | Publication Date |
---|---|
UA62978C2 true UA62978C2 (en) | 2004-01-15 |
Family
ID=8228714
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
UA2000021178A UA62978C2 (en) | 1997-09-08 | 1998-01-09 | Synergistic compositions comprising imazalil and epoxiconazole |
Country Status (20)
Country | Link |
---|---|
US (1) | US6174911B1 (no) |
EP (1) | EP1014792B1 (no) |
AR (1) | AR017071A1 (no) |
AT (1) | ATE241905T1 (no) |
AU (1) | AU741544B2 (no) |
BG (1) | BG64109B1 (no) |
BR (1) | BR9812630A (no) |
CA (1) | CA2302428A1 (no) |
DE (1) | DE69815363D1 (no) |
EE (1) | EE04087B1 (no) |
HU (1) | HUP0003478A3 (no) |
IL (1) | IL134900A (no) |
NO (1) | NO20001170L (no) |
NZ (1) | NZ503118A (no) |
PL (1) | PL339175A1 (no) |
SK (1) | SK2802000A3 (no) |
TR (1) | TR200000623T2 (no) |
UA (1) | UA62978C2 (no) |
WO (1) | WO1999012422A1 (no) |
ZA (1) | ZA988167B (no) |
Families Citing this family (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE50308438D1 (de) * | 2002-07-10 | 2007-11-29 | Basf Ag | Fungizide Mischungen auf Basis von Dithianon |
DE602005002236T2 (de) | 2004-02-04 | 2008-05-15 | Janssen Pharmaceutica N.V. | Synergistische antifungale ddac-zusammensetzungen |
US7753907B2 (en) | 2004-10-29 | 2010-07-13 | Boston Scientific Scimed, Inc. | Medical device systems and methods |
NZ583584A (en) | 2005-09-29 | 2010-05-28 | Janssen Pharmaceutica Nv | Synergistic antifungal combinations of imazalil and fosetyl-Al (aluminum tris(ethyl phosphite)) |
RU2434382C2 (ru) | 2006-03-07 | 2011-11-27 | Янссен Фармацевтика Н.В. | Комбинации имазалила и соединений серебра |
JP2009535377A (ja) | 2006-05-02 | 2009-10-01 | ジヤンセン・フアーマシユーチカ・ナームローゼ・フエンノートシヤツプ | イマザリルを含んでなる殺生物性組み合わせ |
EP2197440B1 (en) * | 2007-08-31 | 2012-12-26 | Janssen Pharmaceutica, N.V. | Combinations of imazalil and hydroxypyridones |
PT2200438E (pt) | 2007-09-07 | 2011-09-30 | Janssen Pharmaceutica Nv | Combinações de pirimetanil e compostos de prata |
EP2242365B1 (en) | 2008-02-06 | 2013-01-16 | Janssen Pharmaceutica NV | Combinations of pyrimethanil and pyrion compounds |
CA2711762C (en) | 2008-02-06 | 2016-11-01 | Jan Pieter Hendrik Bosselaers | Combinations of phenylpyrroles and pyrion compounds |
MX2009002351A (es) | 2008-03-07 | 2009-09-25 | Plant Protectants Llc | Metodos para proteger cultivos de la descomposicion microbiana de post cosecha. |
US9675080B2 (en) | 2009-03-20 | 2017-06-13 | Verdesian Life Sciences U.S., Llc | Methods for delaying maturity of crops |
US9237749B2 (en) | 2010-07-01 | 2016-01-19 | Janssen Pharmaceutica N.V. | Antimicrobial combinations of pyrion compounds with polyethyleneimines |
ES2542246T3 (es) | 2011-03-17 | 2015-08-03 | Ica Laboratories Cc | Composición fungicida |
Family Cites Families (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3658813A (en) | 1970-01-13 | 1972-04-25 | Janssen Pharmaceutica Nv | 1-(beta-aryl-beta-(r-oxy)-ethyl)-imidazoles |
DE2823818C2 (de) | 1978-05-31 | 1987-01-15 | HORA Landwirtschaftliche Betriebsmittel GmbH, 7867 Wehr | Saatgut-Beizmittel und deren Verwendung |
DE2916853A1 (de) | 1979-04-26 | 1980-11-06 | Wacker Chemie Gmbh | Fungizidkombination zur behandlung von getreidesaatgut |
CA1271764A (en) | 1985-03-29 | 1990-07-17 | Stefan Karbach | Azolylmethyloxiranes, their preparation and their use as crop protection agents |
US5013746A (en) * | 1988-04-08 | 1991-05-07 | Janssen Pharmaceutica N.V. | Imazalil containing synergistic compositions |
ES2080063T3 (es) * | 1988-04-08 | 1996-02-01 | Janssen Pharmaceutica Nv | Composiciones sinergicas que contienen imazalil. |
-
1998
- 1998-01-09 UA UA2000021178A patent/UA62978C2/uk unknown
- 1998-09-01 US US09/486,955 patent/US6174911B1/en not_active Expired - Fee Related
- 1998-09-01 NZ NZ503118A patent/NZ503118A/en unknown
- 1998-09-01 EP EP98954263A patent/EP1014792B1/en not_active Expired - Lifetime
- 1998-09-01 PL PL98339175A patent/PL339175A1/xx unknown
- 1998-09-01 TR TR2000/00623T patent/TR200000623T2/xx unknown
- 1998-09-01 BR BR9812630-0A patent/BR9812630A/pt not_active IP Right Cessation
- 1998-09-01 SK SK280-2000A patent/SK2802000A3/sk unknown
- 1998-09-01 DE DE69815363T patent/DE69815363D1/de not_active Expired - Lifetime
- 1998-09-01 HU HU0003478A patent/HUP0003478A3/hu unknown
- 1998-09-01 WO PCT/EP1998/005711 patent/WO1999012422A1/en active IP Right Grant
- 1998-09-01 AU AU11455/99A patent/AU741544B2/en not_active Ceased
- 1998-09-01 CA CA002302428A patent/CA2302428A1/en not_active Abandoned
- 1998-09-01 EE EEP200000099A patent/EE04087B1/xx not_active IP Right Cessation
- 1998-09-01 IL IL13490098A patent/IL134900A/en not_active IP Right Cessation
- 1998-09-01 AT AT98954263T patent/ATE241905T1/de not_active IP Right Cessation
- 1998-09-07 ZA ZA9808167A patent/ZA988167B/xx unknown
- 1998-09-07 AR ARP980104453A patent/AR017071A1/es unknown
-
2000
- 2000-02-28 BG BG104203A patent/BG64109B1/bg active Active
- 2000-03-07 NO NO20001170A patent/NO20001170L/no not_active Application Discontinuation
Also Published As
Publication number | Publication date |
---|---|
BG64109B1 (bg) | 2004-01-30 |
TR200000623T2 (tr) | 2000-08-21 |
NZ503118A (en) | 2001-05-25 |
NO20001170L (no) | 2000-05-02 |
BG104203A (en) | 2001-08-31 |
EE04087B1 (et) | 2003-08-15 |
EP1014792A1 (en) | 2000-07-05 |
EP1014792B1 (en) | 2003-06-04 |
ATE241905T1 (de) | 2003-06-15 |
WO1999012422A1 (en) | 1999-03-18 |
EE200000099A (et) | 2000-12-15 |
DE69815363D1 (de) | 2003-07-10 |
PL339175A1 (en) | 2000-12-04 |
US6174911B1 (en) | 2001-01-16 |
IL134900A (en) | 2004-09-27 |
IL134900A0 (en) | 2001-05-20 |
ZA988167B (en) | 2000-03-22 |
NO20001170D0 (no) | 2000-03-07 |
BR9812630A (pt) | 2000-08-22 |
AU1145599A (en) | 1999-03-29 |
HUP0003478A3 (en) | 2002-01-28 |
AR017071A1 (es) | 2001-08-22 |
AU741544B2 (en) | 2001-12-06 |
SK2802000A3 (en) | 2000-08-14 |
CA2302428A1 (en) | 1999-03-18 |
HUP0003478A2 (hu) | 2001-02-28 |
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