TW200948269A - Emulsifiable concentrate - Google Patents

Emulsifiable concentrate Download PDF

Info

Publication number: TW200948269A
Authority: TW; Taiwan
Prior art keywords: acid; phenol; doc; emulsifier; group
Prior art date: 2008-04-08

Application number

TW98111533A

Other languages

English (en)

Chinese (zh)

Inventor

Cedric Dieleman

Michael Krapp

Ulrich Steinbrenner

Ansgar Schaefer

Steffen Kuhn

Eva Dillmann

Original Assignee

Basf Se

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.)

2008-04-08

Filing date

2009-04-07

Publication date

2009-12-01

2009-04-07 Application filed by Basf Se filed Critical Basf Se

2009-12-01 Publication of TW200948269A publication Critical patent/TW200948269A/zh

Links

239000004495 emulsifiable concentrate Substances 0.000 title claims abstract description 39
239000003995 emulsifying agent Substances 0.000 claims abstract description 88
239000000203 mixture Substances 0.000 claims abstract description 87
238000009472 formulation Methods 0.000 claims abstract description 70
241000233866 Fungi Species 0.000 claims abstract description 24
239000002904 solvent Substances 0.000 claims abstract description 18
238000000034 method Methods 0.000 claims abstract description 15
ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical class OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims abstract description 14
150000003852 triazoles Chemical class 0.000 claims abstract description 14
150000003839 salts Chemical class 0.000 claims abstract description 13
230000000855 fungicidal effect Effects 0.000 claims abstract description 12
239000003960 organic solvent Substances 0.000 claims abstract description 8
239000000654 additive Substances 0.000 claims abstract description 6
-1 ep0XiC0naz0le Chemical compound 0.000 claims description 126
239000002585 base Substances 0.000 claims description 15
229910052739 hydrogen Inorganic materials 0.000 claims description 13
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 12
239000001257 hydrogen Substances 0.000 claims description 12
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 10
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 9
GJYCVCVHRSWLNY-UHFFFAOYSA-N 2-butylphenol Chemical compound CCCCC1=CC=CC=C1O GJYCVCVHRSWLNY-UHFFFAOYSA-N 0.000 claims description 8
150000002989 phenols Chemical class 0.000 claims description 8
239000000126 substance Substances 0.000 claims description 8
ICKWICRCANNIBI-UHFFFAOYSA-N 2,4-di-tert-butylphenol Chemical compound CC(C)(C)C1=CC=C(O)C(C(C)(C)C)=C1 ICKWICRCANNIBI-UHFFFAOYSA-N 0.000 claims description 6
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 6
238000002156 mixing Methods 0.000 claims description 6
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 6
239000005822 Propiconazole Substances 0.000 claims description 5
FBOUIAKEJMZPQG-BLXFFLACSA-N diniconazole-M Chemical compound C1=NC=NN1/C([C@H](O)C(C)(C)C)=C/C1=CC=C(Cl)C=C1Cl FBOUIAKEJMZPQG-BLXFFLACSA-N 0.000 claims description 5
STJLVHWMYQXCPB-UHFFFAOYSA-N propiconazole Chemical compound O1C(CCC)COC1(C=1C(=CC(Cl)=CC=1)Cl)CN1N=CN=C1 STJLVHWMYQXCPB-UHFFFAOYSA-N 0.000 claims description 5
239000005864 Sulphur Substances 0.000 claims description 4
210000003802 sputum Anatomy 0.000 claims description 4
PFEFOYRSMXVNEL-UHFFFAOYSA-N 2,4,6-tritert-butylphenol Chemical compound CC(C)(C)C1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 PFEFOYRSMXVNEL-UHFFFAOYSA-N 0.000 claims description 3
WPVQCZGIVUKPMR-UHFFFAOYSA-N 3-butyl-2,6-ditert-butylphenol Chemical compound CCCCC1=CC=C(C(C)(C)C)C(O)=C1C(C)(C)C WPVQCZGIVUKPMR-UHFFFAOYSA-N 0.000 claims description 3
RQDJADAKIFFEKQ-UHFFFAOYSA-N 4-(4-chlorophenyl)-2-phenyl-2-(1,2,4-triazol-1-ylmethyl)butanenitrile Chemical compound C1=CC(Cl)=CC=C1CCC(C=1C=CC=CC=1)(C#N)CN1N=CN=C1 RQDJADAKIFFEKQ-UHFFFAOYSA-N 0.000 claims description 3
239000005775 Fenbuconazole Substances 0.000 claims description 3
OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 claims description 3
239000005868 Metconazole Substances 0.000 claims description 3
206010036790 Productive cough Diseases 0.000 claims description 3
229910052783 alkali metal Inorganic materials 0.000 claims description 3
AKNQMEBLVAMSNZ-UHFFFAOYSA-N azaconazole Chemical compound ClC1=CC(Cl)=CC=C1C1(CN2N=CN=C2)OCCO1 AKNQMEBLVAMSNZ-UHFFFAOYSA-N 0.000 claims description 3
229950000294 azaconazole Drugs 0.000 claims description 3
UREBDLICKHMUKA-CXSFZGCWSA-N dexamethasone Chemical compound C1CC2=CC(=O)C=C[C@]2(C)[C@]2(F)[C@@H]1[C@@H]1C[C@@H](C)[C@@](C(=O)CO)(O)[C@@]1(C)C[C@@H]2O UREBDLICKHMUKA-CXSFZGCWSA-N 0.000 claims description 3
229960003957 dexamethasone Drugs 0.000 claims description 3
230000002538 fungal effect Effects 0.000 claims description 3
238000010438 heat treatment Methods 0.000 claims description 3
125000003187 heptyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 3
XWPZUHJBOLQNMN-UHFFFAOYSA-N metconazole Chemical compound C1=NC=NN1CC1(O)C(C)(C)CCC1CC1=CC=C(Cl)C=C1 XWPZUHJBOLQNMN-UHFFFAOYSA-N 0.000 claims description 3
208000024794 sputum Diseases 0.000 claims description 3
PPDBOQMNKNNODG-NTEUORMPSA-N (5E)-5-(4-chlorobenzylidene)-2,2-dimethyl-1-(1,2,4-triazol-1-ylmethyl)cyclopentanol Chemical compound C1=NC=NN1CC1(O)C(C)(C)CC\C1=C/C1=CC=C(Cl)C=C1 PPDBOQMNKNNODG-NTEUORMPSA-N 0.000 claims description 2
WURBVZBTWMNKQT-UHFFFAOYSA-N 1-(4-chlorophenoxy)-3,3-dimethyl-1-(1,2,4-triazol-1-yl)butan-2-one Chemical compound C1=NC=NN1C(C(=O)C(C)(C)C)OC1=CC=C(Cl)C=C1 WURBVZBTWMNKQT-UHFFFAOYSA-N 0.000 claims description 2
RMOGWMIKYWRTKW-UHFFFAOYSA-N 1-(4-chlorophenyl)-4,4-dimethyl-2-(1H-1,2,4-triazol-1-yl)pentan-3-ol Chemical compound C1=NC=NN1C(C(O)C(C)(C)C)CC1=CC=C(Cl)C=C1 RMOGWMIKYWRTKW-UHFFFAOYSA-N 0.000 claims description 2
PXMNMQRDXWABCY-UHFFFAOYSA-N 1-(4-chlorophenyl)-4,4-dimethyl-3-(1H-1,2,4-triazol-1-ylmethyl)pentan-3-ol Chemical compound C1=NC=NN1CC(O)(C(C)(C)C)CCC1=CC=C(Cl)C=C1 PXMNMQRDXWABCY-UHFFFAOYSA-N 0.000 claims description 2
VGPIBGGRCVEHQZ-UHFFFAOYSA-N 1-(biphenyl-4-yloxy)-3,3-dimethyl-1-(1,2,4-triazol-1-yl)butan-2-ol Chemical compound C1=NC=NN1C(C(O)C(C)(C)C)OC(C=C1)=CC=C1C1=CC=CC=C1 VGPIBGGRCVEHQZ-UHFFFAOYSA-N 0.000 claims description 2
LQDARGUHUSPFNL-UHFFFAOYSA-N 1-[2-(2,4-dichlorophenyl)-3-(1,1,2,2-tetrafluoroethoxy)propyl]1,2,4-triazole Chemical compound C=1C=C(Cl)C=C(Cl)C=1C(COC(F)(F)C(F)F)CN1C=NC=N1 LQDARGUHUSPFNL-UHFFFAOYSA-N 0.000 claims description 2
MGNFYQILYYYUBS-UHFFFAOYSA-N 1-[3-(4-tert-butylphenyl)-2-methylpropyl]piperidine Chemical compound C=1C=C(C(C)(C)C)C=CC=1CC(C)CN1CCCCC1 MGNFYQILYYYUBS-UHFFFAOYSA-N 0.000 claims description 2
YTOPFCCWCSOHFV-UHFFFAOYSA-N 2,6-dimethyl-4-tridecylmorpholine Chemical compound CCCCCCCCCCCCCN1CC(C)OC(C)C1 YTOPFCCWCSOHFV-UHFFFAOYSA-N 0.000 claims description 2
STMIIPIFODONDC-UHFFFAOYSA-N 2-(2,4-dichlorophenyl)-1-(1H-1,2,4-triazol-1-yl)hexan-2-ol Chemical compound C=1C=C(Cl)C=C(Cl)C=1C(O)(CCCC)CN1C=NC=N1 STMIIPIFODONDC-UHFFFAOYSA-N 0.000 claims description 2
HZJKXKUJVSEEFU-UHFFFAOYSA-N 2-(4-chlorophenyl)-2-(1H-1,2,4-triazol-1-ylmethyl)hexanenitrile Chemical compound C=1C=C(Cl)C=CC=1C(CCCC)(C#N)CN1C=NC=N1 HZJKXKUJVSEEFU-UHFFFAOYSA-N 0.000 claims description 2
UFNOUKDBUJZYDE-UHFFFAOYSA-N 2-(4-chlorophenyl)-3-cyclopropyl-1-(1H-1,2,4-triazol-1-yl)butan-2-ol Chemical compound C1=NC=NN1CC(O)(C=1C=CC(Cl)=CC=1)C(C)C1CC1 UFNOUKDBUJZYDE-UHFFFAOYSA-N 0.000 claims description 2
YABFPHSQTSFWQB-UHFFFAOYSA-N 2-(4-fluorophenyl)-1-(1,2,4-triazol-1-yl)-3-(trimethylsilyl)propan-2-ol Chemical compound C=1C=C(F)C=CC=1C(O)(C[Si](C)(C)C)CN1C=NC=N1 YABFPHSQTSFWQB-UHFFFAOYSA-N 0.000 claims description 2
MNHVNIJQQRJYDH-UHFFFAOYSA-N 2-[2-(1-chlorocyclopropyl)-3-(2-chlorophenyl)-2-hydroxypropyl]-1,2-dihydro-1,2,4-triazole-3-thione Chemical compound N1=CNC(=S)N1CC(C1(Cl)CC1)(O)CC1=CC=CC=C1Cl MNHVNIJQQRJYDH-UHFFFAOYSA-N 0.000 claims description 2
KNDDEFBFJLKPFE-UHFFFAOYSA-N 4-n-Heptylphenol Chemical compound CCCCCCCC1=CC=C(O)C=C1 KNDDEFBFJLKPFE-UHFFFAOYSA-N 0.000 claims description 2
IGFHQQFPSIBGKE-UHFFFAOYSA-N 4-nonylphenol Chemical compound CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 claims description 2
NTDQQZYCCIDJRK-UHFFFAOYSA-N 4-octylphenol Chemical compound CCCCCCCCC1=CC=C(O)C=C1 NTDQQZYCCIDJRK-UHFFFAOYSA-N 0.000 claims description 2
239000005740 Boscalid Substances 0.000 claims description 2
239000005741 Bromuconazole Substances 0.000 claims description 2
239000005757 Cyproconazole Substances 0.000 claims description 2
239000005767 Epoxiconazole Substances 0.000 claims description 2
239000005777 Fenpropidin Substances 0.000 claims description 2
239000005785 Fluquinconazole Substances 0.000 claims description 2
239000005796 Ipconazole Substances 0.000 claims description 2
239000005800 Kresoxim-methyl Substances 0.000 claims description 2
239000005810 Metrafenone Substances 0.000 claims description 2
239000005811 Myclobutanil Substances 0.000 claims description 2
239000005825 Prothioconazole Substances 0.000 claims description 2
239000005839 Tebuconazole Substances 0.000 claims description 2
239000005840 Tetraconazole Substances 0.000 claims description 2
239000005846 Triadimenol Substances 0.000 claims description 2
239000005859 Triticonazole Substances 0.000 claims description 2
150000001340 alkali metals Chemical class 0.000 claims description 2
238000010539 anionic addition polymerization reaction Methods 0.000 claims description 2
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 2
229940118790 boscalid Drugs 0.000 claims description 2
WYEMLYFITZORAB-UHFFFAOYSA-N boscalid Chemical compound C1=CC(Cl)=CC=C1C1=CC=CC=C1NC(=O)C1=CC=CN=C1Cl WYEMLYFITZORAB-UHFFFAOYSA-N 0.000 claims description 2
IJJVMEJXYNJXOJ-UHFFFAOYSA-N fluquinconazole Chemical compound C=1C=C(Cl)C=C(Cl)C=1N1C(=O)C2=CC(F)=CC=C2N=C1N1C=NC=N1 IJJVMEJXYNJXOJ-UHFFFAOYSA-N 0.000 claims description 2
FQKUGOMFVDPBIZ-UHFFFAOYSA-N flusilazole Chemical compound C=1C=C(F)C=CC=1[Si](C=1C=CC(F)=CC=1)(C)CN1C=NC=N1 FQKUGOMFVDPBIZ-UHFFFAOYSA-N 0.000 claims description 2
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 2
AGKSTYPVMZODRV-UHFFFAOYSA-N imibenconazole Chemical compound C1=CC(Cl)=CC=C1CSC(CN1N=CN=C1)=NC1=CC=C(Cl)C=C1Cl AGKSTYPVMZODRV-UHFFFAOYSA-N 0.000 claims description 2
QTYCMDBMOLSEAM-UHFFFAOYSA-N ipconazole Chemical compound C1=NC=NN1CC1(O)C(C(C)C)CCC1CC1=CC=C(Cl)C=C1 QTYCMDBMOLSEAM-UHFFFAOYSA-N 0.000 claims description 2
ZOTBXTZVPHCKPN-HTXNQAPBSA-N kresoxim-methyl Chemical compound CO\N=C(\C(=O)OC)C1=CC=CC=C1COC1=CC=CC=C1C ZOTBXTZVPHCKPN-HTXNQAPBSA-N 0.000 claims description 2
AMSPWOYQQAWRRM-UHFFFAOYSA-N metrafenone Chemical compound COC1=CC=C(Br)C(C)=C1C(=O)C1=C(C)C=C(OC)C(OC)=C1OC AMSPWOYQQAWRRM-UHFFFAOYSA-N 0.000 claims description 2
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 claims description 2
FJBGIXKIXPUXBY-UHFFFAOYSA-N {2-[3-(4-chlorophenyl)propyl]-2,4,4-trimethyl-1,3-oxazolidin-3-yl}(imidazol-1-yl)methanone Chemical compound C1=CN=CN1C(=O)N1C(C)(C)COC1(C)CCCC1=CC=C(Cl)C=C1 FJBGIXKIXPUXBY-UHFFFAOYSA-N 0.000 claims description 2
210000003296 saliva Anatomy 0.000 claims 3
QQOMQLYQAXGHSU-UHFFFAOYSA-N 2,3,6-Trimethylphenol Chemical compound CC1=CC=C(C)C(O)=C1C QQOMQLYQAXGHSU-UHFFFAOYSA-N 0.000 claims 2
UJOBWOGCFQCDNV-UHFFFAOYSA-N 9H-carbazole Chemical compound C1=CC=C2C3=CC=CC=C3NC2=C1 UJOBWOGCFQCDNV-UHFFFAOYSA-N 0.000 claims 2
239000011814 protection agent Substances 0.000 claims 2
YNWVFADWVLCOPU-MDWZMJQESA-N (1E)-1-(4-chlorophenyl)-4,4-dimethyl-2-(1H-1,2,4-triazol-1-yl)pent-1-en-3-ol Chemical compound C1=NC=NN1/C(C(O)C(C)(C)C)=C/C1=CC=C(Cl)C=C1 YNWVFADWVLCOPU-MDWZMJQESA-N 0.000 claims 1
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 claims 1
SJCKVWVUTUYEDN-UHFFFAOYSA-N 1,6-dibutylcyclohexa-2,4-dien-1-ol Chemical compound C(CCC)C1(C(C=CC=C1)CCCC)O SJCKVWVUTUYEDN-UHFFFAOYSA-N 0.000 claims 1
JWUCHKBSVLQQCO-UHFFFAOYSA-N 1-(2-fluorophenyl)-1-(4-fluorophenyl)-2-(1H-1,2,4-triazol-1-yl)ethanol Chemical compound C=1C=C(F)C=CC=1C(C=1C(=CC=CC=1)F)(O)CN1C=NC=N1 JWUCHKBSVLQQCO-UHFFFAOYSA-N 0.000 claims 1
WKBPZYKAUNRMKP-UHFFFAOYSA-N 1-[2-(2,4-dichlorophenyl)pentyl]1,2,4-triazole Chemical compound C=1C=C(Cl)C=C(Cl)C=1C(CCC)CN1C=NC=N1 WKBPZYKAUNRMKP-UHFFFAOYSA-N 0.000 claims 1
DKCPKDPYUFEZCP-UHFFFAOYSA-N 2,6-di-tert-butylphenol Chemical compound CC(C)(C)C1=CC=CC(C(C)(C)C)=C1O DKCPKDPYUFEZCP-UHFFFAOYSA-N 0.000 claims 1
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YQEZLKZALYSWHR-UHFFFAOYSA-N Ketamine Chemical compound C=1C=CC=C(Cl)C=1C1(NC)CCCCC1=O YQEZLKZALYSWHR-UHFFFAOYSA-N 0.000 claims 1
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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
229930185603 trichostatin Natural products 0.000 description 1
RTKIYFITIVXBLE-QEQCGCAPSA-N trichostatin A Chemical compound ONC(=O)/C=C/C(/C)=C/[C@@H](C)C(=O)C1=CC=C(N(C)C)C=C1 RTKIYFITIVXBLE-QEQCGCAPSA-N 0.000 description 1
DQJCHOQLCLEDLL-UHFFFAOYSA-N tricyclazole Chemical compound CC1=CC=CC2=C1N1C=NN=C1S2 DQJCHOQLCLEDLL-UHFFFAOYSA-N 0.000 description 1
229940087291 tridecyl alcohol Drugs 0.000 description 1
125000002889 tridecyl 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])[H] 0.000 description 1
XOALFFJGWSCQEO-UHFFFAOYSA-N tridecyl prop-2-enoate Chemical compound CCCCCCCCCCCCCOC(=O)C=C XOALFFJGWSCQEO-UHFFFAOYSA-N 0.000 description 1
ONCZDRURRATYFI-TVJDWZFNSA-N trifloxystrobin Chemical compound CO\N=C(\C(=O)OC)C1=CC=CC=C1CO\N=C(/C)C1=CC=CC(C(F)(F)F)=C1 ONCZDRURRATYFI-TVJDWZFNSA-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
RVKCCVTVZORVGD-UHFFFAOYSA-N trinexapac-ethyl Chemical group O=C1CC(C(=O)OCC)CC(=O)C1=C(O)C1CC1 RVKCCVTVZORVGD-UHFFFAOYSA-N 0.000 description 1
SBXWFLISHPUINY-UHFFFAOYSA-N triphenyltin Chemical compound C1=CC=CC=C1[Sn](C=1C=CC=CC=1)C1=CC=CC=C1 SBXWFLISHPUINY-UHFFFAOYSA-N 0.000 description 1
ZNISUIPMIHJFRZ-UHFFFAOYSA-N triphenyltin;hydrochloride Chemical compound Cl.C1=CC=CC=C1[Sn](C=1C=CC=CC=1)C1=CC=CC=C1 ZNISUIPMIHJFRZ-UHFFFAOYSA-N 0.000 description 1
239000001226 triphosphate Substances 0.000 description 1
235000011178 triphosphate Nutrition 0.000 description 1
UNXRWKVEANCORM-UHFFFAOYSA-I triphosphate(5-) Chemical compound [O-]P([O-])(=O)OP([O-])(=O)OP([O-])([O-])=O UNXRWKVEANCORM-UHFFFAOYSA-I 0.000 description 1
UNXRWKVEANCORM-UHFFFAOYSA-N triphosphoric acid Chemical compound OP(O)(=O)OP(O)(=O)OP(O)(O)=O UNXRWKVEANCORM-UHFFFAOYSA-N 0.000 description 1
150000003648 triterpenes Chemical class 0.000 description 1
GPRLSGONYQIRFK-MNYXATJNSA-N triton Chemical compound [3H+] GPRLSGONYQIRFK-MNYXATJNSA-N 0.000 description 1
239000002753 trypsin inhibitor Substances 0.000 description 1
231100000397 ulcer Toxicity 0.000 description 1
125000002948 undecyl 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])[H] 0.000 description 1
JARYYMUOCXVXNK-CSLFJTBJSA-N validamycin A Chemical compound N([C@H]1C[C@@H]([C@H]([C@H](O)[C@H]1O)O[C@H]1[C@@H]([C@@H](O)[C@H](O)[C@@H](CO)O1)O)CO)[C@H]1C=C(CO)[C@@H](O)[C@H](O)[C@H]1O JARYYMUOCXVXNK-CSLFJTBJSA-N 0.000 description 1
DBXFMOWZRXXBRN-LWKPJOBUSA-N valifenalate Chemical compound CC(C)OC(=O)N[C@@H](C(C)C)C(=O)NC(CC(=O)OC)C1=CC=C(Cl)C=C1 DBXFMOWZRXXBRN-LWKPJOBUSA-N 0.000 description 1
239000008158 vegetable oil Substances 0.000 description 1
210000003462 vein Anatomy 0.000 description 1
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
229920003169 water-soluble polymer Polymers 0.000 description 1
238000009333 weeding Methods 0.000 description 1
241000228158 x Triticosecale Species 0.000 description 1
239000000230 xanthan gum Substances 0.000 description 1
229920001285 xanthan gum Polymers 0.000 description 1
235000010493 xanthan gum Nutrition 0.000 description 1
229940082509 xanthan gum Drugs 0.000 description 1
239000000811 xylitol Substances 0.000 description 1
HEBKCHPVOIAQTA-SCDXWVJYSA-N xylitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)CO HEBKCHPVOIAQTA-SCDXWVJYSA-N 0.000 description 1
235000010447 xylitol Nutrition 0.000 description 1
229960002675 xylitol Drugs 0.000 description 1
DUBNHZYBDBBJHD-UHFFFAOYSA-L ziram Chemical compound [Zn+2].CN(C)C([S-])=S.CN(C)C([S-])=S DUBNHZYBDBBJHD-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
- A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
- A01N25/02—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests containing liquids as carriers, diluents or solvents

Landscapes

Life Sciences & Earth Sciences (AREA)
General Health & Medical Sciences (AREA)
Health & Medical Sciences (AREA)
Toxicology (AREA)
Pest Control & Pesticides (AREA)
Plant Pathology (AREA)
Agronomy & Crop Science (AREA)
Engineering & Computer Science (AREA)
Dentistry (AREA)
Wood Science & Technology (AREA)
Zoology (AREA)
Environmental Sciences (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)

TW98111533A 2008-04-08 2009-04-07 Emulsifiable concentrate TW200948269A (en)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
EP08154192		2008-04-08
EP08154238		2008-04-09

Publications (1)

Publication Number	Publication Date
TW200948269A true TW200948269A (en)	2009-12-01

Family

ID=41162294

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
TW98111533A TW200948269A (en)	2008-04-08	2009-04-07	Emulsifiable concentrate

Country Status (9)

Country	Link
EP (1)	EP2303006A2 (es)
CN (1)	CN102014617B (es)
AR (1)	AR071465A1 (es)
BR (1)	BRPI0910402A2 (es)
CR (1)	CR11694A (es)
EA (1)	EA017661B1 (es)
MX (1)	MX2010010335A (es)
TW (1)	TW200948269A (es)
WO (1)	WO2009124920A2 (es)

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* Cited by examiner, † Cited by third party
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CN102613217B (zh) *	2011-02-01	2013-10-16	石河子大学	一种抗植物病原真菌组合物及其制备方法
RU2572201C1 (ru) *	2014-09-29	2015-12-27	Общество с ограниченной ответственностью "Доктор Фармер Инвест"	Фунгицидный протравитель семян "турион"
CA2993486C (en) *	2015-07-27	2023-12-12	Basf Se	Emulsifiable concentrate comprising triazole fungicide, fatty acid amide and aromatic hydrocarbon
UA107869U (uk) *	2015-12-21	2016-06-24	Товариство З Обмеженою Відповідальністю "Альфа Хімгруп"	Фунгіцидна композиція для передпосівної обробки насіння пшениці
CN106879589A (zh) *	2016-12-30	2017-06-23	新昌县派特普科技有限公司	草坪护理用杀菌剂专用有机硅生化助剂
US11834466B2 (en)	2017-11-30	2023-12-05	5Metis, Inc.	Benzoxaborole compounds and formulations thereof
GB2584044B (en) *	2018-01-05	2022-08-31	Mi Llc	Invert emulsion gravel packing fluid for alternate path technology
WO2019245934A1 (en) *	2018-06-19	2019-12-26	M-I L.L.C.	Invert emulsion screen running fluid stability and reversibility control
US11236115B2 (en)	2018-08-18	2022-02-01	5Metis, Inc.	Solid forms of substituted benzoxaborole and compositions thereof
CN110074129A (zh) *	2019-05-10	2019-08-02	南京荣诚化工有限公司	一种结合辛硫磷高效氯氟氰菊酯的可溶液剂
CN111066800A (zh) *	2019-12-26	2020-04-28	安徽久易农业股份有限公司	一种丙硫菌唑系列乳油及其制备方法和应用
US12534678B2 (en) *	2020-11-04	2026-01-27	Basf Se	Aqueous emulsifier package with anionic surfactant for fuel emulsion
UY39548A (es) *	2020-12-01	2022-06-30	Adama Makhteshim Ltd	Composiciones estabilizadas que contienen fungicidas de estrobilurina y alcoholes polihídricos
WO2022238999A1 (en) *	2021-05-10	2022-11-17	Adama Agan Ltd.	Stable agrochemical suspension concentrate compositions

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Publication number	Priority date	Publication date	Assignee	Title
BE619550A (es) *	1961-06-30
JPS5675409A (en) *	1979-11-26	1981-06-22	Sumitomo Chem Co Ltd	Emulsion composition for herbicidal use
US4411694A (en) *	1980-06-03	1983-10-25	American Cyanamid Company	Emulsifiable concentrates of 2-chloro-N-isopropyl-2',3'-dimethylacetanilide with improved resistance to crystallization and process for preparing the same
CS253719B2 (en) *	1984-03-07	1987-12-17	Janssen Pharmaceutica Nv	Emulsible concentrate with fungicide activity and process for preparing thereof
EP0357559B1 (de) *	1988-09-02	1994-10-19	AgrEvo UK Limited	Wässrige Formulierungen und deren Verwendung
DE4108871A1 (de) *	1991-03-19	1992-09-24	Hoechst Ag	Waessrige formulierung von prochloraz, ihre herstellung und ihre verwendung
US6872736B1 (en) *	2000-01-26	2005-03-29	Basf Aktiengesellschaft	Non-aqueous emulsifiable concentrate formulation
EP1205108A3 (de) *	2000-10-02	2002-06-12	Bayer Ag	Wirkstoffhaltige Emulsionen

2009
- 2009-04-07 WO PCT/EP2009/054113 patent/WO2009124920A2/en not_active Ceased
- 2009-04-07 AR ARP090101238 patent/AR071465A1/es unknown
- 2009-04-07 TW TW98111533A patent/TW200948269A/zh unknown
- 2009-04-07 CN CN200980115847.1A patent/CN102014617B/zh not_active Expired - Fee Related
- 2009-04-07 MX MX2010010335A patent/MX2010010335A/es unknown
- 2009-04-07 BR BRPI0910402-0A patent/BRPI0910402A2/pt not_active Application Discontinuation
- 2009-04-07 EP EP09729458A patent/EP2303006A2/en not_active Withdrawn
- 2009-04-07 EA EA201001575A patent/EA017661B1/ru not_active IP Right Cessation
2010
- 2010-09-27 CR CR11694A patent/CR11694A/es unknown

Also Published As

Publication number	Publication date
AR071465A1 (es)	2010-06-23
MX2010010335A (es)	2010-10-04
CR11694A (es)	2011-01-10
EA201001575A1 (ru)	2011-04-29
EP2303006A2 (en)	2011-04-06
BRPI0910402A2 (pt)	2015-07-28
CN102014617B (zh)	2014-10-01
EA017661B1 (ru)	2013-02-28
WO2009124920A2 (en)	2009-10-15
CN102014617A (zh)	2011-04-13
WO2009124920A3 (en)	2010-04-08

Publication	Publication Date	Title
TW200948269A (en)	2009-12-01	Emulsifiable concentrate
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JP5920983B2 (ja)	2016-05-24	有害菌類を防除するための組み合わせにおける合成殺菌剤および生物学的殺菌剤の使用
US20110105323A1 (en)	2011-05-05	Calcium Salts of Phosphorous Acid for Increasing the Effect of Fungicides
CN102448295B (zh)	2015-11-25	防治有害真菌的方法
JP2011522005A (ja)	2011-07-28	相乗作用的殺菌剤混合物
JP5422560B2 (ja)	2014-02-19	殺菌剤混合物
ES2557902T3 (es)	2016-01-29	Composiciones fungicidas que comprenden 3'-bromo-2,3,4,6'-tetrametoxi-2'-6-dimetilbenzofenona
AU2008300639B2 (en)	2012-11-01	Fungicidal mixtures of triticonazole and difenoconazole
CN102480937B (zh)	2014-12-10	悬浮乳液农药组合物