IL134900A - Synergistic preparations containing imzalil and epoxyconzole - Google Patents

Synergistic preparations containing imzalil and epoxyconzole

Info

Publication number: IL134900A
Authority: IL; Israel
Prior art keywords: imazalil; epoxiconazole; salt; composition; active ingredients
Prior art date: 1997-09-08

Application number

IL13490098A

Other languages

English (en)

Hebrew (he)

Other versions

IL134900A0 (en

Original Assignee

Janssen Pharmaceutica Nv

Priority date (The priority date 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 date listed.)

1997-09-08

Filing date

1998-09-01

Publication date

2004-09-27

1998-09-01 Application filed by Janssen Pharmaceutica Nv filed Critical Janssen Pharmaceutica Nv

2001-05-20 Publication of IL134900A0 publication Critical patent/IL134900A0/xx

2004-09-27 Publication of IL134900A publication Critical patent/IL134900A/en

Links

239000000203 mixture Substances 0.000 title claims abstract description 84
229960002125 enilconazole Drugs 0.000 title claims abstract description 28
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 27
239000005795 Imazalil Substances 0.000 title claims abstract description 27
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 claims abstract description 23
239000005767 Epoxiconazole Substances 0.000 title claims abstract description 23
230000002195 synergetic effect Effects 0.000 title claims abstract description 14
150000003839 salts Chemical class 0.000 claims abstract description 28
230000000843 anti-fungal effect Effects 0.000 claims abstract description 9
239000004480 active ingredient Substances 0.000 claims description 37
235000013399 edible fruits Nutrition 0.000 claims description 13
241000233866 Fungi Species 0.000 claims description 9
239000012141 concentrate Substances 0.000 claims description 6
239000004495 emulsifiable concentrate Substances 0.000 claims description 5
239000004546 suspension concentrate Substances 0.000 claims description 5
229940121375 antifungal agent Drugs 0.000 claims description 4
239000004550 soluble concentrate Substances 0.000 claims description 3
238000004519 manufacturing process Methods 0.000 claims 1
-1 hydrofluoric Chemical class 0.000 description 36
241000196324 Embryophyta Species 0.000 description 31
150000001875 compounds Chemical class 0.000 description 28
239000004094 surface-active agent Substances 0.000 description 15
238000009472 formulation Methods 0.000 description 14
NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonium chloride Substances [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 9
229910052751 metal Inorganic materials 0.000 description 9
239000002184 metal Substances 0.000 description 9
239000003760 tallow Substances 0.000 description 9
239000000969 carrier Substances 0.000 description 8
239000007788 liquid Substances 0.000 description 8
235000014113 dietary fatty acids Nutrition 0.000 description 7
239000000194 fatty acid Substances 0.000 description 7
229930195729 fatty acid Natural products 0.000 description 7
238000011282 treatment Methods 0.000 description 7
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 6
239000002671 adjuvant Substances 0.000 description 6
239000002585 base Substances 0.000 description 6
125000004432 carbon atom Chemical group C* 0.000 description 6
125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 6
239000000047 product Substances 0.000 description 6
239000007787 solid Substances 0.000 description 6
239000000126 substance Substances 0.000 description 6
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
239000002253 acid Substances 0.000 description 5
239000000654 additive Substances 0.000 description 5
125000000217 alkyl group Chemical group 0.000 description 5
235000019270 ammonium chloride Nutrition 0.000 description 5
239000012895 dilution Substances 0.000 description 5
238000010790 dilution Methods 0.000 description 5
235000019441 ethanol Nutrition 0.000 description 5
238000011081 inoculation Methods 0.000 description 5
239000002917 insecticide Substances 0.000 description 5
239000002736 nonionic surfactant Substances 0.000 description 5
150000003904 phospholipids Chemical class 0.000 description 5
150000003242 quaternary ammonium salts Chemical class 0.000 description 5
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 4
DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 4
150000001298 alcohols Chemical class 0.000 description 4
239000003240 coconut oil Substances 0.000 description 4
235000019864 coconut oil Nutrition 0.000 description 4
235000008504 concentrate Nutrition 0.000 description 4
150000004665 fatty acids Chemical class 0.000 description 4
239000003337 fertilizer Substances 0.000 description 4
230000002538 fungal effect Effects 0.000 description 4
229930195733 hydrocarbon Natural products 0.000 description 4
229910052708 sodium Inorganic materials 0.000 description 4
239000011734 sodium Substances 0.000 description 4
239000002689 soil Substances 0.000 description 4
239000002904 solvent Substances 0.000 description 4
239000004215 Carbon black (E152) Substances 0.000 description 3
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
229910019142 PO4 Inorganic materials 0.000 description 3
QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 3
150000007513 acids Chemical class 0.000 description 3
150000003863 ammonium salts Chemical class 0.000 description 3
239000007798 antifreeze agent Substances 0.000 description 3
XKXHCNPAFAXVRZ-UHFFFAOYSA-N benzylazanium;chloride Chemical compound [Cl-].[NH3+]CC1=CC=CC=C1 XKXHCNPAFAXVRZ-UHFFFAOYSA-N 0.000 description 3
125000002091 cationic group Chemical group 0.000 description 3
235000020971 citrus fruits Nutrition 0.000 description 3
239000010949 copper Substances 0.000 description 3
239000002270 dispersing agent Substances 0.000 description 3
150000002170 ethers Chemical class 0.000 description 3
239000012669 liquid formulation Substances 0.000 description 3
150000002739 metals Chemical class 0.000 description 3
238000000034 method Methods 0.000 description 3
235000021317 phosphate Nutrition 0.000 description 3
239000000843 powder Substances 0.000 description 3
125000001273 sulfonato group Chemical class [O-]S(*)(=O)=O 0.000 description 3
150000003467 sulfuric acid derivatives Chemical class 0.000 description 3
230000009885 systemic effect Effects 0.000 description 3
229960004546 thiabendazole Drugs 0.000 description 3
239000004308 thiabendazole Substances 0.000 description 3
WJCNZQLZVWNLKY-UHFFFAOYSA-N thiabendazole Chemical compound S1C=NC(C=2NC3=CC=CC=C3N=2)=C1 WJCNZQLZVWNLKY-UHFFFAOYSA-N 0.000 description 3
235000010296 thiabendazole Nutrition 0.000 description 3
239000002562 thickening agent Substances 0.000 description 3
239000000080 wetting agent Substances 0.000 description 3
QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 2
235000016068 Berberis vulgaris Nutrition 0.000 description 2
241000335053 Beta vulgaris Species 0.000 description 2
229910021532 Calcite Inorganic materials 0.000 description 2
RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 2
240000008067 Cucumis sativus Species 0.000 description 2
241000219104 Cucurbitaceae Species 0.000 description 2
IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
241000159512 Geotrichum Species 0.000 description 2
244000168141 Geotrichum candidum Species 0.000 description 2
235000017388 Geotrichum candidum Nutrition 0.000 description 2
235000010469 Glycine max Nutrition 0.000 description 2
244000068988 Glycine max Species 0.000 description 2
XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
241001465754 Metazoa Species 0.000 description 2
SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 2
PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
229920003171 Poly (ethylene oxide) Polymers 0.000 description 2
239000002250 absorbent Substances 0.000 description 2
230000002745 absorbent Effects 0.000 description 2
230000000895 acaricidal effect Effects 0.000 description 2
239000000642 acaricide Substances 0.000 description 2
239000000853 adhesive Substances 0.000 description 2
230000001070 adhesive effect Effects 0.000 description 2
229910052783 alkali metal Inorganic materials 0.000 description 2
150000008055 alkyl aryl sulfonates Chemical class 0.000 description 2
239000003945 anionic surfactant Substances 0.000 description 2
239000004599 antimicrobial Substances 0.000 description 2
239000011230 binding agent Substances 0.000 description 2
VEMKTZHHVJILDY-UXHICEINSA-N bioresmethrin Chemical compound CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)OCC1=COC(CC=2C=CC=CC=2)=C1 VEMKTZHHVJILDY-UXHICEINSA-N 0.000 description 2
230000015572 biosynthetic process Effects 0.000 description 2
159000000007 calcium salts Chemical class 0.000 description 2
239000003093 cationic surfactant Substances 0.000 description 2
239000004464 cereal grain Substances 0.000 description 2
235000013339 cereals Nutrition 0.000 description 2
SXPWTBGAZSPLHA-UHFFFAOYSA-M cetalkonium chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCC[N+](C)(C)CC1=CC=CC=C1 SXPWTBGAZSPLHA-UHFFFAOYSA-M 0.000 description 2
229910052802 copper Inorganic materials 0.000 description 2
JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
229960002483 decamethrin Drugs 0.000 description 2
OWZREIFADZCYQD-NSHGMRRFSA-N deltamethrin Chemical compound CC1(C)[C@@H](C=C(Br)Br)[C@H]1C(=O)O[C@H](C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 OWZREIFADZCYQD-NSHGMRRFSA-N 0.000 description 2
DOIRQSBPFJWKBE-UHFFFAOYSA-N dibutyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 description 2
230000000694 effects Effects 0.000 description 2
239000000839 emulsion Substances 0.000 description 2
238000011156 evaluation Methods 0.000 description 2
238000002474 experimental method Methods 0.000 description 2
NYPJDWWKZLNGGM-UHFFFAOYSA-N fenvalerate Chemical compound C=1C=C(Cl)C=CC=1C(C(C)C)C(=O)OC(C#N)C(C=1)=CC=CC=1OC1=CC=CC=C1 NYPJDWWKZLNGGM-UHFFFAOYSA-N 0.000 description 2
230000000855 fungicidal effect Effects 0.000 description 2
239000000417 fungicide Substances 0.000 description 2
239000008187 granular material Substances 0.000 description 2
239000004009 herbicide Substances 0.000 description 2
239000002054 inoculum Substances 0.000 description 2
229910052500 inorganic mineral Inorganic materials 0.000 description 2
239000000463 material Substances 0.000 description 2
230000003641 microbiacidal effect Effects 0.000 description 2
244000005700 microbiome Species 0.000 description 2
239000011707 mineral Substances 0.000 description 2
238000002156 mixing Methods 0.000 description 2
239000005645 nematicide Substances 0.000 description 2
125000000913 palmityl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
150000003013 phosphoric acid derivatives Chemical class 0.000 description 2
239000005648 plant growth regulator Substances 0.000 description 2
229920000151 polyglycol Polymers 0.000 description 2
239000010695 polyglycol Substances 0.000 description 2
229920000642 polymer Polymers 0.000 description 2
150000003254 radicals Chemical class 0.000 description 2
SMQUZDBALVYZAC-UHFFFAOYSA-N salicylaldehyde Chemical compound OC1=CC=CC=C1C=O SMQUZDBALVYZAC-UHFFFAOYSA-N 0.000 description 2
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 2
239000000344 soap Substances 0.000 description 2
239000000243 solution Substances 0.000 description 2
239000012453 solvate Substances 0.000 description 2
235000012424 soybean oil Nutrition 0.000 description 2
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235000020354 squash Nutrition 0.000 description 2
238000003786 synthesis reaction Methods 0.000 description 2
230000007704 transition Effects 0.000 description 2
235000015112 vegetable and seed oil Nutrition 0.000 description 2
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239000001993 wax Substances 0.000 description 2
ZCVAOQKBXKSDMS-AQYZNVCMSA-N (+)-trans-allethrin Chemical compound CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)OC1C(C)=C(CC=C)C(=O)C1 ZCVAOQKBXKSDMS-AQYZNVCMSA-N 0.000 description 1
SNICXCGAKADSCV-JTQLQIEISA-N (-)-Nicotine Chemical compound CN1CCC[C@H]1C1=CC=CN=C1 SNICXCGAKADSCV-JTQLQIEISA-N 0.000 description 1
KAATUXNTWXVJKI-NSHGMRRFSA-N (1R)-cis-(alphaS)-cypermethrin Chemical compound CC1(C)[C@@H](C=C(Cl)Cl)[C@H]1C(=O)O[C@H](C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 KAATUXNTWXVJKI-NSHGMRRFSA-N 0.000 description 1
YATDSXRLIUJOQN-SVRRBLITSA-N (2,3,4,5,6-pentafluorophenyl)methyl (1r,3s)-3-(2,2-dichloroethenyl)-2,2-dimethylcyclopropane-1-carboxylate Chemical compound CC1(C)[C@H](C=C(Cl)Cl)[C@H]1C(=O)OCC1=C(F)C(F)=C(F)C(F)=C1F YATDSXRLIUJOQN-SVRRBLITSA-N 0.000 description 1
OMFJOGRNNTZSQQ-UHFFFAOYSA-N (2-butan-2-ylphenyl)methylcarbamic acid Chemical compound CCC(C)C1=CC=CC=C1CNC(O)=O OMFJOGRNNTZSQQ-UHFFFAOYSA-N 0.000 description 1
JNYAEWCLZODPBN-JGWLITMVSA-N (2r,3r,4s)-2-[(1r)-1,2-dihydroxyethyl]oxolane-3,4-diol Chemical compound OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O JNYAEWCLZODPBN-JGWLITMVSA-N 0.000 description 1
ASWBNKHCZGQVJV-UHFFFAOYSA-N (3-hexadecanoyloxy-2-hydroxypropyl) 2-(trimethylazaniumyl)ethyl phosphate Chemical compound CCCCCCCCCCCCCCCC(=O)OCC(O)COP([O-])(=O)OCC[N+](C)(C)C ASWBNKHCZGQVJV-UHFFFAOYSA-N 0.000 description 1
WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
KANAPVJGZDNSCZ-UHFFFAOYSA-N 1,2-benzothiazole 1-oxide Chemical class C1=CC=C2S(=O)N=CC2=C1 KANAPVJGZDNSCZ-UHFFFAOYSA-N 0.000 description 1
TZCPCKNHXULUIY-RGULYWFUSA-N 1,2-distearoyl-sn-glycero-3-phosphoserine Chemical compound CCCCCCCCCCCCCCCCCC(=O)OC[C@H](COP(O)(=O)OC[C@H](N)C(O)=O)OC(=O)CCCCCCCCCCCCCCCCC TZCPCKNHXULUIY-RGULYWFUSA-N 0.000 description 1
IIZPXYDJLKNOIY-JXPKJXOSSA-N 1-palmitoyl-2-arachidonoyl-sn-glycero-3-phosphocholine Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCC\C=C/C\C=C/C\C=C/C\C=C/CCCCC IIZPXYDJLKNOIY-JXPKJXOSSA-N 0.000 description 1
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GUXWVUVLXIJHQF-UHFFFAOYSA-N 2,5-dibromophenol Chemical compound OC1=CC(Br)=CC=C1Br GUXWVUVLXIJHQF-UHFFFAOYSA-N 0.000 description 1
RANCECPPZPIPNO-UHFFFAOYSA-N 2,5-dichlorophenol Chemical compound OC1=CC(Cl)=CC=C1Cl RANCECPPZPIPNO-UHFFFAOYSA-N 0.000 description 1
XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical group COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 description 1
JDSQBDGCMUXRBM-UHFFFAOYSA-N 2-[2-(2-butoxypropoxy)propoxy]propan-1-ol Chemical group CCCCOC(C)COC(C)COC(C)CO JDSQBDGCMUXRBM-UHFFFAOYSA-N 0.000 description 1
CFWRDBDJAOHXSH-SECBINFHSA-N 2-azaniumylethyl [(2r)-2,3-diacetyloxypropyl] phosphate Chemical compound CC(=O)OC[C@@H](OC(C)=O)COP(O)(=O)OCCN CFWRDBDJAOHXSH-SECBINFHSA-N 0.000 description 1
NCKMMSIFQUPKCK-UHFFFAOYSA-N 2-benzyl-4-chlorophenol Chemical compound OC1=CC=C(Cl)C=C1CC1=CC=CC=C1 NCKMMSIFQUPKCK-UHFFFAOYSA-N 0.000 description 1
WBIQQQGBSDOWNP-UHFFFAOYSA-N 2-dodecylbenzenesulfonic acid Chemical class CCCCCCCCCCCCC1=CC=CC=C1S(O)(=O)=O WBIQQQGBSDOWNP-UHFFFAOYSA-N 0.000 description 1
QCDWFXQBSFUVSP-UHFFFAOYSA-N 2-phenoxyethanol Chemical compound OCCOC1=CC=CC=C1 QCDWFXQBSFUVSP-UHFFFAOYSA-N 0.000 description 1
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GBNHEBQXJVDXSW-UHFFFAOYSA-N 3,4,5-trichlorophenol Chemical compound OC1=CC(Cl)=C(Cl)C(Cl)=C1 GBNHEBQXJVDXSW-UHFFFAOYSA-N 0.000 description 1
PZFMWYNHJFZBPO-UHFFFAOYSA-N 3,5-dibromophenol Chemical compound OC1=CC(Br)=CC(Br)=C1 PZFMWYNHJFZBPO-UHFFFAOYSA-N 0.000 description 1
VPOMSPZBQMDLTM-UHFFFAOYSA-N 3,5-dichlorophenol Chemical compound OC1=CC(Cl)=CC(Cl)=C1 VPOMSPZBQMDLTM-UHFFFAOYSA-N 0.000 description 1
FOGYNLXERPKEGN-UHFFFAOYSA-N 3-(2-hydroxy-3-methoxyphenyl)-2-[2-methoxy-4-(3-sulfopropyl)phenoxy]propane-1-sulfonic acid Chemical compound COC1=CC=CC(CC(CS(O)(=O)=O)OC=2C(=CC(CCCS(O)(=O)=O)=CC=2)OC)=C1O FOGYNLXERPKEGN-UHFFFAOYSA-N 0.000 description 1
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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
150000004671 saturated fatty acids Chemical class 0.000 description 1
235000003441 saturated fatty acids Nutrition 0.000 description 1
229910052624 sepiolite Inorganic materials 0.000 description 1
235000019355 sepiolite Nutrition 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
238000005507 spraying Methods 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 Chemical class 0.000 description 1
238000004659 sterilization and disinfection Methods 0.000 description 1
239000004575 stone Substances 0.000 description 1
235000021012 strawberries Nutrition 0.000 description 1
125000001424 substituent group Chemical group 0.000 description 1
125000000542 sulfonic acid group Chemical group 0.000 description 1
150000003460 sulfonic acids Chemical class 0.000 description 1
239000000375 suspending agent Substances 0.000 description 1
239000000725 suspension Substances 0.000 description 1
239000000454 talc Substances 0.000 description 1
235000012222 talc Nutrition 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
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
AMFGTOFWMRQMEM-UHFFFAOYSA-N triazophos Chemical compound N1=C(OP(=S)(OCC)OCC)N=CN1C1=CC=CC=C1 AMFGTOFWMRQMEM-UHFFFAOYSA-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
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
150000004670 unsaturated fatty acids Chemical class 0.000 description 1
235000021122 unsaturated fatty acids Nutrition 0.000 description 1
150000003672 ureas Chemical class 0.000 description 1
235000013311 vegetables Nutrition 0.000 description 1
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
229920002554 vinyl polymer Polymers 0.000 description 1
238000009736 wetting Methods 0.000 description 1
239000002023 wood Substances 0.000 description 1
150000003751 zinc Chemical class 0.000 description 1
239000011701 zinc Substances 0.000 description 1
229910052725 zinc Inorganic materials 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)
Dentistry (AREA)
Pest Control & Pesticides (AREA)
Plant Pathology (AREA)
Health & Medical Sciences (AREA)
Engineering & Computer Science (AREA)
Agronomy & Crop Science (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)

IL13490098A 1997-09-08 1998-09-01 Synergistic preparations containing imzalil and epoxyconzole IL134900A (en)

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 (2)

Publication Number	Publication Date
IL134900A0 IL134900A0 (en)	2001-05-20
IL134900A true IL134900A (en)	2004-09-27

Family

ID=8228714

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
IL13490098A IL134900A (en)	1997-09-08	1998-09-01	Synergistic preparations containing imzalil and epoxyconzole

Country Status (20)

Country	Link
US (1)	US6174911B1 (de)
EP (1)	EP1014792B1 (de)
AR (1)	AR017071A1 (de)
AT (1)	ATE241905T1 (de)
AU (1)	AU741544B2 (de)
BG (1)	BG64109B1 (de)
BR (1)	BR9812630A (de)
CA (1)	CA2302428A1 (de)
DE (1)	DE69815363D1 (de)
EE (1)	EE04087B1 (de)
HU (1)	HUP0003478A3 (de)
IL (1)	IL134900A (de)
NO (1)	NO20001170L (de)
NZ (1)	NZ503118A (de)
PL (1)	PL339175A1 (de)
SK (1)	SK2802000A3 (de)
TR (1)	TR200000623T2 (de)
UA (1)	UA62978C2 (de)
WO (1)	WO1999012422A1 (de)
ZA (1)	ZA988167B (de)

Families Citing this family (14)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
AU2003246635A1 (en) *	2002-07-10	2004-02-02	Basf Aktiengesellschaft	Fungicidal mixtures based on dithianon
CA2554236C (en)	2004-02-04	2012-09-11	Janssen Pharmaceutica N.V.	Synergistic antifungal didecyl dimethyl ammonium chloride compositions
US7753907B2 (en)	2004-10-29	2010-07-13	Boston Scientific Scimed, Inc.	Medical device systems and methods
CA2622114A1 (en) *	2005-09-29	2007-04-12	Janssen Pharmaceutica N.V.	Synergistic imazalil combinations
JP5199891B2 (ja)	2006-03-07	2013-05-15	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	イマザリルと銀化合物との組み合わせ
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
US8921403B2 (en) *	2007-08-31	2014-12-30	Janssen Pharmaceutica, Nv	Combinations of imazalil and hydroxypyridones
EP2200438B1 (de)	2007-09-07	2011-07-13	Janssen Pharmaceutica NV	Kombinationen aus pyrimethanil und silberverbindungen
US8575187B2 (en)	2008-02-06	2013-11-05	Janssen Pharmaceutica, Nv	Combinations of anilinopyrimidines and pyrion compounds
US8043422B2 (en)	2008-02-06	2011-10-25	Janssen Pharmaceutica, Nv	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
ES2602481T3 (es)	2010-07-01	2017-02-21	Janssen Pharmaceutica, N.V.	Combinaciones antimicrobianas de compuestos de piriona con polietileniminas
ES2542246T3 (es)	2011-03-17	2015-08-03	Ica Laboratories Cc	Composición fungicida

Family Cites Families (6)

* Cited by examiner, † Cited by third party
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
IL78175A (en)	1985-03-29	1989-10-31	Basf Ag	Azolylmethyloxiranes,their preparation and their use as fungicide 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 EP EP98954263A patent/EP1014792B1/de not_active Expired - Lifetime
- 1998-09-01 WO PCT/EP1998/005711 patent/WO1999012422A1/en not_active Ceased
- 1998-09-01 SK SK280-2000A patent/SK2802000A3/sk unknown
- 1998-09-01 AU AU11455/99A patent/AU741544B2/en not_active Ceased
- 1998-09-01 BR BR9812630-0A patent/BR9812630A/pt not_active IP Right Cessation
- 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 DE DE69815363T patent/DE69815363D1/de 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 AT AT98954263T patent/ATE241905T1/de not_active IP Right Cessation
- 1998-09-01 US US09/486,955 patent/US6174911B1/en not_active Expired - Fee Related
- 1998-09-01 HU HU0003478A patent/HUP0003478A3/hu unknown
- 1998-09-01 NZ NZ503118A patent/NZ503118A/en unknown
- 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 unknown
- 2000-03-07 NO NO20001170A patent/NO20001170L/no not_active Application Discontinuation

Also Published As

Publication number	Publication date
BG104203A (en)	2001-08-31
NO20001170D0 (no)	2000-03-07
PL339175A1 (en)	2000-12-04
AU1145599A (en)	1999-03-29
TR200000623T2 (tr)	2000-08-21
EE04087B1 (et)	2003-08-15
ATE241905T1 (de)	2003-06-15
BG64109B1 (bg)	2004-01-30
WO1999012422A1 (en)	1999-03-18
AU741544B2 (en)	2001-12-06
EP1014792A1 (de)	2000-07-05
EP1014792B1 (de)	2003-06-04
IL134900A0 (en)	2001-05-20
NO20001170L (no)	2000-05-02
CA2302428A1 (en)	1999-03-18
US6174911B1 (en)	2001-01-16
HUP0003478A2 (hu)	2001-02-28
HUP0003478A3 (en)	2002-01-28
UA62978C2 (en)	2004-01-15
NZ503118A (en)	2001-05-25
ZA988167B (en)	2000-03-22
DE69815363D1 (de)	2003-07-10
AR017071A1 (es)	2001-08-22
EE200000099A (et)	2000-12-15
BR9812630A (pt)	2000-08-22
SK2802000A3 (en)	2000-08-14

Legal Events

Date	Code	Title	Description
2005-02-20	FF	Patent granted
2006-01-15	MM9K	Patent not in force due to non-payment of renewal fees

Publication	Publication Date	Title
US5397795A (en)	1995-03-14	Synergistic compositions containing propiconazole and tebuconazole
CA2193364C (en)	2007-02-13	Synergistic compositions containing metconazole and another triazole
US5223524A (en)	1993-06-29	Synergistic compositions containing propiconazole and tebuconazole
EP1713331B1 (de)	2007-08-29	Synergistische antifungale ddac-zusammensetzungen
IL190447A (en)	2014-06-30	An agricultural preparation containing imazilil and boscalid and methods for preparing it
EP1014792B1 (de)	2003-06-04	Imazalil und epoxiconazol beinhaltende synergistische zusammensetzungen
EP0336489B1 (de)	1995-08-23	Imazalil enthaltende synergistische Zusammensetzungen
US5013746A (en)	1991-05-07	Imazalil containing synergistic compositions
MXPA00002346A (en)	2002-03-05	Synergistic compositions comprising imazalil and epoxiconazole
CZ2000702A3 (cs)	2000-06-14	Synergické prostředky obsahující imazalil a epoxiconazol
HK1010703B (en)	2002-03-22	Synergistic compositions containing metconazole and another triazole
HK1079401B (en)	2009-06-05	Formulations comprising triazoles and alkoxylated amines
HK1079401A1 (zh)	2006-04-07	含有三唑和烷氧化胺的制剂