SK3662001A3 - Non-aqueous suspension concentrate - Google Patents

Non-aqueous suspension concentrate Download PDF

Info

Publication number: SK3662001A3
Authority: SK; Slovakia
Prior art keywords: suspension concentrate; concentrate according; optionally; compounds; active
Prior art date: 1998-09-25

Application number

SK366-2001A

Other languages

English (en)

Slovak (sk)

Inventor

Michael Aven

Original Assignee

Basf Ag

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.)

1998-09-25

Filing date

1999-09-22

Publication date

2001-11-06

Family has litigation

First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=22578753&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=SK3662001(A3) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.

1999-09-22 Application filed by Basf Ag filed Critical Basf Ag

2001-11-06 Publication of SK3662001A3 publication Critical patent/SK3662001A3/sk

Links

239000007900 aqueous suspension Substances 0.000 title description 14
239000012141 concentrate Substances 0.000 title description 14
150000001875 compounds Chemical class 0.000 claims abstract description 51
239000002270 dispersing agent Substances 0.000 claims abstract description 26
239000004546 suspension concentrate Substances 0.000 claims abstract description 23
239000003960 organic solvent Substances 0.000 claims abstract description 7
239000002671 adjuvant Substances 0.000 claims abstract description 6
125000000129 anionic group Chemical group 0.000 claims abstract description 6
239000002562 thickening agent Substances 0.000 claims abstract description 6
-1 alkyl lactates Chemical class 0.000 claims description 41
239000000203 mixture Substances 0.000 claims description 40
239000004480 active ingredient Substances 0.000 claims description 26
239000000546 pharmaceutical excipient Substances 0.000 claims description 23
238000009472 formulation Methods 0.000 claims description 17
150000001412 amines Chemical class 0.000 claims description 7
125000005843 halogen group Chemical group 0.000 claims description 6
238000000034 method Methods 0.000 claims description 6
238000002360 preparation method Methods 0.000 claims description 6
150000003626 triacylglycerols Chemical class 0.000 claims description 6
229910052783 alkali metal Inorganic materials 0.000 claims description 5
150000001340 alkali metals Chemical class 0.000 claims description 5
150000002148 esters Chemical class 0.000 claims description 5
150000002334 glycols Chemical class 0.000 claims description 5
YWBFPKPWMSWWEA-UHFFFAOYSA-O triazolopyrimidine Chemical class BrC1=CC=CC(C=2N=C3N=CN[N+]3=C(NCC=3C=CN=CC=3)C=2)=C1 YWBFPKPWMSWWEA-UHFFFAOYSA-O 0.000 claims description 5
235000015112 vegetable and seed oil Nutrition 0.000 claims description 5
239000008158 vegetable oil Substances 0.000 claims description 5
229920003171 Poly (ethylene oxide) Polymers 0.000 claims description 4
241000607479 Yersinia pestis Species 0.000 claims description 4
150000001298 alcohols Chemical class 0.000 claims description 4
229910052784 alkaline earth metal Inorganic materials 0.000 claims description 4
125000000217 alkyl group Chemical group 0.000 claims description 4
150000004945 aromatic hydrocarbons Chemical class 0.000 claims description 4
235000014113 dietary fatty acids Nutrition 0.000 claims description 4
239000000194 fatty acid Substances 0.000 claims description 4
229930195729 fatty acid Natural products 0.000 claims description 4
150000004665 fatty acids Chemical class 0.000 claims description 4
238000000227 grinding Methods 0.000 claims description 4
125000000623 heterocyclic group Chemical group 0.000 claims description 4
229910052739 hydrogen Inorganic materials 0.000 claims description 4
238000002156 mixing Methods 0.000 claims description 4
229910052757 nitrogen Inorganic materials 0.000 claims description 4
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 4
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 3
239000000654 additive Substances 0.000 claims description 3
125000003118 aryl group Chemical group 0.000 claims description 3
125000000753 cycloalkyl group Chemical group 0.000 claims description 3
238000007865 diluting Methods 0.000 claims description 3
239000001257 hydrogen Substances 0.000 claims description 3
125000004433 nitrogen atom Chemical group N* 0.000 claims description 3
UFTFJSFQGQCHQW-UHFFFAOYSA-N triformin Chemical compound O=COCC(OC=O)COC=O UFTFJSFQGQCHQW-UHFFFAOYSA-N 0.000 claims description 3
230000000996 additive effect Effects 0.000 claims description 2
125000003342 alkenyl group Chemical group 0.000 claims description 2
125000003545 alkoxy group Chemical group 0.000 claims description 2
125000000304 alkynyl group Chemical group 0.000 claims description 2
150000001602 bicycloalkyls Chemical group 0.000 claims description 2
238000004090 dissolution Methods 0.000 claims description 2
125000001188 haloalkyl group Chemical group 0.000 claims description 2
125000001072 heteroaryl group Chemical group 0.000 claims description 2
150000004760 silicates Chemical class 0.000 claims description 2
125000000547 substituted alkyl group Chemical group 0.000 claims description 2
230000000361 pesticidal effect Effects 0.000 abstract description 4
239000000725 suspension Substances 0.000 abstract description 3
229920002257 Plurafac® Polymers 0.000 description 13
239000003795 chemical substances by application Substances 0.000 description 10
241000196324 Embryophyta Species 0.000 description 7
239000004615 ingredient Substances 0.000 description 7
239000002245 particle Substances 0.000 description 7
238000010790 dilution Methods 0.000 description 6
239000012895 dilution Substances 0.000 description 6
239000007921 spray Substances 0.000 description 6
239000002904 solvent Substances 0.000 description 5
239000000126 substance Substances 0.000 description 5
239000004094 surface-active agent Substances 0.000 description 5
CNPVJWYWYZMPDS-UHFFFAOYSA-N 2-methyldecane Chemical compound CCCCCCCCC(C)C CNPVJWYWYZMPDS-UHFFFAOYSA-N 0.000 description 4
LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 4
125000004432 carbon atom Chemical group C* 0.000 description 4
239000006185 dispersion Substances 0.000 description 4
230000000855 fungicidal effect Effects 0.000 description 4
239000000417 fungicide Substances 0.000 description 4
230000012010 growth Effects 0.000 description 4
JGHZJRVDZXSNKQ-UHFFFAOYSA-N methyl octanoate Chemical compound CCCCCCCC(=O)OC JGHZJRVDZXSNKQ-UHFFFAOYSA-N 0.000 description 4
RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 3
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 3
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
125000001931 aliphatic group Chemical group 0.000 description 3
150000001338 aliphatic hydrocarbons Chemical class 0.000 description 3
239000000828 canola oil Substances 0.000 description 3
235000019519 canola oil Nutrition 0.000 description 3
239000004359 castor oil Substances 0.000 description 3
235000019438 castor oil Nutrition 0.000 description 3
229910052802 copper Inorganic materials 0.000 description 3
239000010949 copper Substances 0.000 description 3
150000002191 fatty alcohols Chemical class 0.000 description 3
ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 3
239000004009 herbicide Substances 0.000 description 3
239000007788 liquid Substances 0.000 description 3
239000000575 pesticide Substances 0.000 description 3
239000007787 solid Substances 0.000 description 3
238000003860 storage Methods 0.000 description 3
OVSKIKFHRZPJSS-UHFFFAOYSA-N 2,4-D Chemical compound OC(=O)COC1=CC=C(Cl)C=C1Cl OVSKIKFHRZPJSS-UHFFFAOYSA-N 0.000 description 2
FECDACOUYKFOOP-UHFFFAOYSA-N 2-ethylhexyl 2-hydroxypropanoate Chemical compound CCCCC(CC)COC(=O)C(C)O FECDACOUYKFOOP-UHFFFAOYSA-N 0.000 description 2
241000894006 Bacteria Species 0.000 description 2
KZBUYRJDOAKODT-UHFFFAOYSA-N Chlorine Chemical compound ClCl KZBUYRJDOAKODT-UHFFFAOYSA-N 0.000 description 2
MTBZIGHNGSTDJV-UHFFFAOYSA-N Ditalimfos Chemical compound C1=CC=C2C(=O)N(P(=S)(OCC)OCC)C(=O)C2=C1 MTBZIGHNGSTDJV-UHFFFAOYSA-N 0.000 description 2
PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 2
241000233866 Fungi Species 0.000 description 2
239000005562 Glyphosate Substances 0.000 description 2
241000238631 Hexapoda Species 0.000 description 2
241000244206 Nematoda Species 0.000 description 2
PVNIIMVLHYAWGP-UHFFFAOYSA-N Niacin Chemical compound OC(=O)C1=CC=CN=C1 PVNIIMVLHYAWGP-UHFFFAOYSA-N 0.000 description 2
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
239000005624 Tralkoxydim Substances 0.000 description 2
241000700605 Viruses Species 0.000 description 2
SRSXLGNVWSONIS-UHFFFAOYSA-N benzenesulfonic acid Chemical compound OS(=O)(=O)C1=CC=CC=C1 SRSXLGNVWSONIS-UHFFFAOYSA-N 0.000 description 2
OOCMUZJPDXYRFD-UHFFFAOYSA-L calcium;2-dodecylbenzenesulfonate Chemical compound [Ca+2].CCCCCCCCCCCCC1=CC=CC=C1S([O-])(=O)=O.CCCCCCCCCCCCC1=CC=CC=C1S([O-])(=O)=O OOCMUZJPDXYRFD-UHFFFAOYSA-L 0.000 description 2
229910052801 chlorine Inorganic materials 0.000 description 2
YPHMISFOHDHNIV-FSZOTQKASA-N cycloheximide Chemical compound C1[C@@H](C)C[C@H](C)C(=O)[C@@H]1[C@H](O)CC1CC(=O)NC(=O)C1 YPHMISFOHDHNIV-FSZOTQKASA-N 0.000 description 2
239000003085 diluting agent Substances 0.000 description 2
201000010099 disease Diseases 0.000 description 2
208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 2
238000004821 distillation Methods 0.000 description 2
LZCLXQDLBQLTDK-UHFFFAOYSA-N ethyl 2-hydroxypropanoate Chemical compound CCOC(=O)C(C)O LZCLXQDLBQLTDK-UHFFFAOYSA-N 0.000 description 2
BFWMWWXRWVJXSE-UHFFFAOYSA-M fentin hydroxide Chemical compound C=1C=CC=CC=1[Sn](C=1C=CC=CC=1)(O)C1=CC=CC=C1 BFWMWWXRWVJXSE-UHFFFAOYSA-M 0.000 description 2
229910052731 fluorine Inorganic materials 0.000 description 2
239000011737 fluorine Substances 0.000 description 2
229940060367 inert ingredients Drugs 0.000 description 2
239000002917 insecticide Substances 0.000 description 2
NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 2
244000005700 microbiome Species 0.000 description 2
238000012986 modification Methods 0.000 description 2
230000004048 modification Effects 0.000 description 2
239000005645 nematicide Substances 0.000 description 2
CWKFPEBMTGKLKX-UHFFFAOYSA-N picolinafen Chemical compound C1=CC(F)=CC=C1NC(=O)C1=CC=CC(OC=2C=C(C=CC=2)C(F)(F)F)=N1 CWKFPEBMTGKLKX-UHFFFAOYSA-N 0.000 description 2
230000008635 plant growth Effects 0.000 description 2
239000003755 preservative agent Substances 0.000 description 2
MFOUDYKPLGXPGO-UHFFFAOYSA-N propachlor Chemical compound ClCC(=O)N(C(C)C)C1=CC=CC=C1 MFOUDYKPLGXPGO-UHFFFAOYSA-N 0.000 description 2
230000001681 protective effect Effects 0.000 description 2
239000005871 repellent Substances 0.000 description 2
230000002940 repellent Effects 0.000 description 2
238000005507 spraying Methods 0.000 description 2
UCSJYZPVAKXKNQ-HZYVHMACSA-N streptomycin Chemical compound CN[C@H]1[C@H](O)[C@@H](O)[C@H](CO)O[C@H]1O[C@@H]1[C@](C=O)(O)[C@H](C)O[C@H]1O[C@@H]1[C@@H](NC(N)=N)[C@H](O)[C@@H](NC(N)=N)[C@H](O)[C@H]1O UCSJYZPVAKXKNQ-HZYVHMACSA-N 0.000 description 2
239000008399 tap water Substances 0.000 description 2
235000020679 tap water Nutrition 0.000 description 2
XLNZEKHULJKQBA-UHFFFAOYSA-N terbufos Chemical compound CCOP(=S)(OCC)SCSC(C)(C)C XLNZEKHULJKQBA-UHFFFAOYSA-N 0.000 description 2
238000012360 testing method Methods 0.000 description 2
DQFPEYARZIQXRM-LTGZKZEYSA-N tralkoxydim Chemical compound C1C(=O)C(C(/CC)=N/OCC)=C(O)CC1C1=C(C)C=C(C)C=C1C DQFPEYARZIQXRM-LTGZKZEYSA-N 0.000 description 2
239000000080 wetting agent Substances 0.000 description 2
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
XERJKGMBORTKEO-VZUCSPMQSA-N (1e)-2-(ethylcarbamoylamino)-n-methoxy-2-oxoethanimidoyl cyanide Chemical compound CCNC(=O)NC(=O)C(\C#N)=N\OC XERJKGMBORTKEO-VZUCSPMQSA-N 0.000 description 1
NHOWDZOIZKMVAI-UHFFFAOYSA-N (2-chlorophenyl)(4-chlorophenyl)pyrimidin-5-ylmethanol Chemical compound C=1N=CN=CC=1C(C=1C(=CC=CC=1)Cl)(O)C1=CC=C(Cl)C=C1 NHOWDZOIZKMVAI-UHFFFAOYSA-N 0.000 description 1
RYAUSSKQMZRMAI-ALOPSCKCSA-N (2S,6R)-4-[3-(4-tert-butylphenyl)-2-methylpropyl]-2,6-dimethylmorpholine Chemical compound C=1C=C(C(C)(C)C)C=CC=1CC(C)CN1C[C@H](C)O[C@H](C)C1 RYAUSSKQMZRMAI-ALOPSCKCSA-N 0.000 description 1
CXNPLSGKWMLZPZ-GIFSMMMISA-N (2r,3r,6s)-3-[[(3s)-3-amino-5-[carbamimidoyl(methyl)amino]pentanoyl]amino]-6-(4-amino-2-oxopyrimidin-1-yl)-3,6-dihydro-2h-pyran-2-carboxylic acid Chemical compound O1[C@@H](C(O)=O)[C@H](NC(=O)C[C@@H](N)CCN(C)C(N)=N)C=C[C@H]1N1C(=O)N=C(N)C=C1 CXNPLSGKWMLZPZ-GIFSMMMISA-N 0.000 description 1
RLLPVAHGXHCWKJ-HKUYNNGSSA-N (3-phenoxyphenyl)methyl (1r,3r)-3-(2,2-dichloroethenyl)-2,2-dimethylcyclopropane-1-carboxylate Chemical compound CC1(C)[C@@H](C=C(Cl)Cl)[C@H]1C(=O)OCC1=CC=CC(OC=2C=CC=CC=2)=C1 RLLPVAHGXHCWKJ-HKUYNNGSSA-N 0.000 description 1
LDVVMCZRFWMZSG-OLQVQODUSA-N (3ar,7as)-2-(trichloromethylsulfanyl)-3a,4,7,7a-tetrahydroisoindole-1,3-dione Chemical compound C1C=CC[C@H]2C(=O)N(SC(Cl)(Cl)Cl)C(=O)[C@H]21 LDVVMCZRFWMZSG-OLQVQODUSA-N 0.000 description 1
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 description 1
CKPCAYZTYMHQEX-NBVRZTHBSA-N (e)-1-(2,4-dichlorophenyl)-n-methoxy-2-pyridin-3-ylethanimine Chemical compound C=1C=C(Cl)C=C(Cl)C=1C(=N/OC)/CC1=CC=CN=C1 CKPCAYZTYMHQEX-NBVRZTHBSA-N 0.000 description 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 description 1
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 description 1
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 description 1
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 description 1
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 description 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 description 1
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 description 1
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 description 1
RRQYJINTUHWNHW-UHFFFAOYSA-N 1-ethoxy-2-(2-ethoxyethoxy)ethane Chemical compound CCOCCOCCOCC RRQYJINTUHWNHW-UHFFFAOYSA-N 0.000 description 1
125000004206 2,2,2-trifluoroethyl group Chemical group [H]C([H])(*)C(F)(F)F 0.000 description 1
YUBCVMNXGPVXID-UHFFFAOYSA-N 2,2-dichloro-3,3-dimethylcyclopropane-1-carboxylic acid Chemical compound CC1(C)C(C(O)=O)C1(Cl)Cl YUBCVMNXGPVXID-UHFFFAOYSA-N 0.000 description 1
SVPKNMBRVBMTLB-UHFFFAOYSA-N 2,3-dichloronaphthalene-1,4-dione Chemical compound C1=CC=C2C(=O)C(Cl)=C(Cl)C(=O)C2=C1 SVPKNMBRVBMTLB-UHFFFAOYSA-N 0.000 description 1
239000002794 2,4-DB Substances 0.000 description 1
239000005631 2,4-Dichlorophenoxyacetic acid Substances 0.000 description 1
YTOPFCCWCSOHFV-UHFFFAOYSA-N 2,6-dimethyl-4-tridecylmorpholine Chemical compound CCCCCCCCCCCCCN1CC(C)OC(C)C1 YTOPFCCWCSOHFV-UHFFFAOYSA-N 0.000 description 1
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 description 1
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 description 1
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 description 1
NUPJIGQFXCQJBK-UHFFFAOYSA-N 2-(4-isopropyl-4-methyl-5-oxo-4,5-dihydro-1H-imidazol-2-yl)-5-(methoxymethyl)nicotinic acid Chemical compound OC(=O)C1=CC(COC)=CN=C1C1=NC(C)(C(C)C)C(=O)N1 NUPJIGQFXCQJBK-UHFFFAOYSA-N 0.000 description 1
CLQMBPJKHLGMQK-UHFFFAOYSA-N 2-(4-isopropyl-4-methyl-5-oxo-4,5-dihydro-1H-imidazol-2-yl)nicotinic acid Chemical compound N1C(=O)C(C(C)C)(C)N=C1C1=NC=CC=C1C(O)=O CLQMBPJKHLGMQK-UHFFFAOYSA-N 0.000 description 1
GOCUAJYOYBLQRH-UHFFFAOYSA-N 2-(4-{[3-chloro-5-(trifluoromethyl)pyridin-2-yl]oxy}phenoxy)propanoic acid Chemical compound C1=CC(OC(C)C(O)=O)=CC=C1OC1=NC=C(C(F)(F)F)C=C1Cl GOCUAJYOYBLQRH-UHFFFAOYSA-N 0.000 description 1
YUVKUEAFAVKILW-UHFFFAOYSA-N 2-(4-{[5-(trifluoromethyl)pyridin-2-yl]oxy}phenoxy)propanoic acid Chemical compound C1=CC(OC(C)C(O)=O)=CC=C1OC1=CC=C(C(F)(F)F)C=N1 YUVKUEAFAVKILW-UHFFFAOYSA-N 0.000 description 1
UWHURBUBIHUHSU-UHFFFAOYSA-N 2-[(4-methoxy-6-methyl-1,3,5-triazin-2-yl)carbamoylsulfamoyl]benzoic acid Chemical compound COC1=NC(C)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)C(O)=O)=N1 UWHURBUBIHUHSU-UHFFFAOYSA-N 0.000 description 1
OOLBCHYXZDXLDS-UHFFFAOYSA-N 2-[4-(2,4-dichlorophenoxy)phenoxy]propanoic acid Chemical compound C1=CC(OC(C)C(O)=O)=CC=C1OC1=CC=C(Cl)C=C1Cl OOLBCHYXZDXLDS-UHFFFAOYSA-N 0.000 description 1
MPPOHAUSNPTFAJ-UHFFFAOYSA-N 2-[4-[(6-chloro-1,3-benzoxazol-2-yl)oxy]phenoxy]propanoic acid Chemical compound C1=CC(OC(C)C(O)=O)=CC=C1OC1=NC2=CC=C(Cl)C=C2O1 MPPOHAUSNPTFAJ-UHFFFAOYSA-N 0.000 description 1
IAJOBQBIJHVGMQ-UHFFFAOYSA-N 2-amino-4-[hydroxy(methyl)phosphoryl]butanoic acid Chemical compound CP(O)(=O)CCC(N)C(O)=O IAJOBQBIJHVGMQ-UHFFFAOYSA-N 0.000 description 1
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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
NKNFWVNSBIXGLL-UHFFFAOYSA-N triazamate Chemical compound CCOC(=O)CSC1=NC(C(C)(C)C)=NN1C(=O)N(C)C NKNFWVNSBIXGLL-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
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
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
230000000007 visual effect Effects 0.000 description 1
239000008096 xylene Substances 0.000 description 1
150000003738 xylenes Chemical class 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
- A01N25/04—Dispersions, emulsions, suspoemulsions, suspension concentrates or gels
- 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
- A01N43/90—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having two or more relevant hetero rings, condensed among themselves or with a common carbocyclic ring system

Landscapes

Life Sciences & Earth Sciences (AREA)
General Health & Medical Sciences (AREA)
Health & Medical Sciences (AREA)
Zoology (AREA)
Dentistry (AREA)
Environmental Sciences (AREA)
Pest Control & Pesticides (AREA)
Plant Pathology (AREA)
Wood Science & Technology (AREA)
Engineering & Computer Science (AREA)
Agronomy & Crop Science (AREA)
Toxicology (AREA)
Chemical & Material Sciences (AREA)
Dispersion Chemistry (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Saccharide Compounds (AREA)
Catching Or Destruction (AREA)

SK366-2001A 1998-09-25 1999-09-22 Non-aqueous suspension concentrate SK3662001A3 (en)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
US16085698A	1998-09-25	1998-09-25
PCT/US1999/022046 WO2000018227A1 (fr)	1998-09-25	1999-09-22	Suspension concentree non aqueuse

Publications (1)

Publication Number	Publication Date
SK3662001A3 true SK3662001A3 (en)	2001-11-06

Family

ID=22578753

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
SK366-2001A SK3662001A3 (en)	1998-09-25	1999-09-22	Non-aqueous suspension concentrate

Country Status (22)

Country	Link
EP (1)	EP1130962B1 (fr)
JP (1)	JP2002525291A (fr)
KR (1)	KR100689910B1 (fr)
CN (1)	CN1215764C (fr)
AT (1)	ATE258009T1 (fr)
AU (1)	AU765664B2 (fr)
BR (1)	BR9913922A (fr)
CA (1)	CA2345296A1 (fr)
CZ (1)	CZ20011057A3 (fr)
DE (1)	DE69914364T2 (fr)
DK (1)	DK1130962T3 (fr)
ES (1)	ES2214890T3 (fr)
HU (1)	HUP0103741A3 (fr)
IL (1)	IL142084A (fr)
NZ (1)	NZ510741A (fr)
PL (1)	PL346870A1 (fr)
PT (1)	PT1130962E (fr)
RU (1)	RU2224434C2 (fr)
SK (1)	SK3662001A3 (fr)
UA (1)	UA70965C2 (fr)
WO (1)	WO2000018227A1 (fr)
ZA (1)	ZA200102411B (fr)

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CN1192707C (zh)	1999-10-26	2005-03-16	陶氏益农有限责任公司	除草剂的浓悬浮剂
WO2002015697A2 (fr) *	2000-08-25	2002-02-28	Basf Aktiengesellschaft	Preparation fongicide
JP5025053B2 (ja) *	2001-08-23	2012-09-12	日本化薬株式会社	小川型農薬製剤
IL148684A (en) *	2002-03-14	2006-12-31	Yoel Sasson	Pesticidal composition
UA78586C2 (en) *	2002-07-18	2007-04-10	Basf Ag	Fungicidal mixture, using thereof, agent and method for controlling pathogenic fungi
JP2007506744A (ja)	2003-09-24	2007-03-22	ワイス・ホールディングズ・コーポレイション	抗癌剤としての６−［（置換）フェニル］トリアゾロピリミジン類
US7419982B2 (en)	2003-09-24	2008-09-02	Wyeth Holdings Corporation	Crystalline forms of 5-chloro-6-{2,6-difluoro-4-[3-(methylamino)propoxy]phenyl}-N-[(1S)-2,2,2-trifluoro-1-methylethyl][1,2,4]triazolo[1,5-a]pyrimidin-7-amine salts
AU2004275728A1 (en)	2003-09-24	2005-04-07	Wyeth Holdings Corporation	6-aryl-7-halo-imidazo[1,2-a]pyrimidines as anticancer agent
JP2007520511A (ja) *	2004-02-06	2007-07-26	バイエルクロップサイエンスゲーエムベーハー	植物保護組成物およびその使用
DE102004011007A1 (de) *	2004-03-06	2005-09-22	Bayer Cropscience Ag	Suspensionskonzentrate auf Ölbasis
US7651977B2 (en) *	2004-10-28	2010-01-26	Valent U.S.A. Corporation	Herbicidal compositions
CN101232814A (zh) *	2005-07-27	2008-07-30	巴斯福股份公司	基于唑并嘧啶基胺的杀真菌混合物
DE102005042876A1 (de)	2005-09-09	2007-03-22	Bayer Cropscience Ag	Verwendung von Laktatestern zur Verbesserung der Wirkung von Pflanzenschutzmitteln
TWI324908B (en) *	2006-01-05	2010-05-21	Du Pont	Liquid formulations of carboxamide arthropodicides
BRPI0717239A2 (pt) *	2006-09-30	2013-10-08	Bayer Cropscience Ag	Concentrados de suspensão para melhorar a absorção da raiz de substâncias ativas agroquímicas
EP1905302A1 (fr) *	2006-09-30	2008-04-02	Bayer CropScience AG	Suspensions concentrées
EP1905300A1 (fr) *	2006-09-30	2008-04-02	Bayer CropScience AG	Compositions phytosanitaires dispersables dans l' eau comprenant des polyalkoxytriglycerides en tant que promoteurs de pénétration
WO2009118025A1 (fr) *	2008-03-27	2009-10-01	Bayer Cropscience Aktiengesellschaft	Procédé permettant de contrôler les animaux nuisibles et les champignons pathogènes nuisibles pour les plantes en appliquant une composition agrochimique dans le milieu de culture, formule appropriée et son utilisation
WO2009118027A1 (fr) *	2008-03-27	2009-10-01	Bayer Cropscience Aktiengesellschaft	Concentrés en suspension pour améliorer l’absorption par les racines de composés agrochimiques actifs
US20110086760A1 (en)	2008-05-28	2011-04-14	Victor Casana Giner	Suspension concentrates in oil of sulfonylureas and combinations with fluroxypyr or other agrochemicals
BR112012018072B1 (pt) *	2010-02-12	2018-10-30	Basf Se	formulação anidra e método para controlar fungos fitopatogênicos
EP2563115B1 (fr) *	2010-04-26	2017-11-08	Dow AgroSciences, LLC	Dispersions agricoles stabilisées à base d'huile
WO2013014126A1 (fr)	2011-07-26	2013-01-31	Bayer Intellectual Property Gmbh	Esters de lactate ethérés, procédé de préparation et leur utilisation pour améliorer l'effet d'agents phytoprotecteurs
JP6088552B2 (ja) *	2012-03-13	2017-03-01	ビーエーエスエフソシエタス・ヨーロピアＢａｓｆＳｅ	ピリピロペン殺虫剤ｉｉｉ含有液体濃厚製剤
BR102013009504A2 (pt) *	2013-04-18	2015-03-17	Oxiteno S A Indústria E Comércio	Formulação agroquímica do tipo dispersão em óleo, uso das formulações agroquímicas do tipo dispersão em óleo e processo de obtenção de formulação agroquímica do tipo dispersão em óleo
GB201405271D0 (en) *	2014-03-25	2014-05-07	Croda Int Plc	Agrochemical oil based concentrates

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GB2083360B (en) *	1980-09-03	1983-09-21	Dow Chemical Co	Solvent-flowable compositions containing a substituted urea insecticide
DE3130633A1 (de) *	1981-08-01	1983-02-17	Basf Ag, 6700 Ludwigshafen	7-amino-azolo(1,5-a)pyrimidine und diese enthaltende fungizide
JPS5929604A (ja) *	1982-08-13	1984-02-16	Nissan Chem Ind Ltd	水性懸濁除草組成物
IT1173066B (it) *	1984-01-18	1987-06-18	Sipcam Spa	Sospensione fluida stabilizzata di antiparassitari in solventi organici non clorurati e procedimento di preparazione e di impiego della stessa
JP2569342B2 (ja) *	1987-10-22	1997-01-08	石原産業株式会社	除草懸濁状組成物
KR910019503A (ko) *	1990-05-10	1991-12-19	후루까와 도요히꼬	수면 직접 시용(施用) 유성 현탁제제
EP0645083B1 (fr) *	1993-09-28	1999-02-03	American Cyanamid Company	Compositions concentrées de suspensions émulsionnables d'acides imidazolinyl benzoiques, leur esters et leurs sels et de dinitroanilines herbicides
DE19605786A1 (de) *	1996-02-16	1997-08-21	Hoechst Schering Agrevo Gmbh	Ölsuspensionskonzentrate
JPH11322517A (ja) *	1998-03-17	1999-11-24	American Cyanamid Co	トリアゾロピリミジン類の効力の増進

1999
- 1999-09-22 NZ NZ510741A patent/NZ510741A/en unknown
- 1999-09-22 PL PL99346870A patent/PL346870A1/xx not_active IP Right Cessation
- 1999-09-22 KR KR1020017003789A patent/KR100689910B1/ko not_active Expired - Fee Related
- 1999-09-22 CN CN998114057A patent/CN1215764C/zh not_active Expired - Fee Related
- 1999-09-22 WO PCT/US1999/022046 patent/WO2000018227A1/fr not_active Ceased
- 1999-09-22 SK SK366-2001A patent/SK3662001A3/sk unknown
- 1999-09-22 BR BR9913922-7A patent/BR9913922A/pt not_active Application Discontinuation
- 1999-09-22 IL IL14208499A patent/IL142084A/xx not_active IP Right Cessation
- 1999-09-22 DK DK99949806T patent/DK1130962T3/da active
- 1999-09-22 EP EP99949806A patent/EP1130962B1/fr not_active Revoked
- 1999-09-22 CA CA002345296A patent/CA2345296A1/fr not_active Abandoned
- 1999-09-22 AU AU62601/99A patent/AU765664B2/en not_active Ceased
- 1999-09-22 HU HU0103741A patent/HUP0103741A3/hu unknown
- 1999-09-22 ES ES99949806T patent/ES2214890T3/es not_active Expired - Lifetime
- 1999-09-22 JP JP2000571755A patent/JP2002525291A/ja not_active Withdrawn
- 1999-09-22 CZ CZ20011057A patent/CZ20011057A3/cs unknown
- 1999-09-22 RU RU2001111328/12A patent/RU2224434C2/ru not_active IP Right Cessation
- 1999-09-22 PT PT99949806T patent/PT1130962E/pt unknown
- 1999-09-22 UA UA2001042823A patent/UA70965C2/uk unknown
- 1999-09-22 AT AT99949806T patent/ATE258009T1/de not_active IP Right Cessation
- 1999-09-22 DE DE69914364T patent/DE69914364T2/de not_active Revoked
2001
- 2001-03-23 ZA ZA200102411A patent/ZA200102411B/en unknown

Also Published As

Publication number	Publication date
IL142084A (en)	2005-12-18
EP1130962A1 (fr)	2001-09-12
ZA200102411B (en)	2002-03-25
ATE258009T1 (de)	2004-02-15
WO2000018227A1 (fr)	2000-04-06
NZ510741A (en)	2003-08-29
KR20010106488A (ko)	2001-11-29
ES2214890T3 (es)	2004-09-16
DE69914364D1 (de)	2004-02-26
IL142084A0 (en)	2002-03-10
DE69914364T2 (de)	2004-07-22
PT1130962E (pt)	2004-04-30
HUP0103741A2 (hu)	2002-01-28
DK1130962T3 (da)	2004-05-17
RU2224434C2 (ru)	2004-02-27
EP1130962B1 (fr)	2004-01-21
UA70965C2 (uk)	2004-11-15
JP2002525291A (ja)	2002-08-13
AU765664B2 (en)	2003-09-25
AU6260199A (en)	2000-04-17
KR100689910B1 (ko)	2007-03-09
CN1215764C (zh)	2005-08-24
CN1320015A (zh)	2001-10-31
CZ20011057A3 (cs)	2002-05-15
BR9913922A (pt)	2002-04-23
HUP0103741A3 (en)	2004-09-28
CA2345296A1 (fr)	2000-04-06
PL346870A1 (en)	2002-03-11

Publication	Publication Date	Title
SK3662001A3 (en)	2001-11-06	Non-aqueous suspension concentrate
US6383984B1 (en)	2002-05-07	Aqueous suspension concentrate
US6165940A (en)	2000-12-26	Non-aqueous suspension concentrate
EP2912945B1 (fr)	2018-10-10	Concentré de suspension comprenant du tébuconazole
EP1023832A1 (fr)	2000-08-02	Suspension aqueuse concentrée
CN1284453C (zh)	2006-11-15	可微乳化的农用化学品浓缩物
US6566308B1 (en)	2003-05-20	Emulsifiable concentrate containing one or more pesticides and adjuvants
PL206592B1 (pl)	2010-08-31	Koncentraty zawiesinowe na bazie oleju, sposób ich wytwarzania i ich zastosowanie
EP0933025A1 (fr)	1999-08-04	Concentré émulsifiable contenant un ou plusieurs pesticides
EP1025757B1 (fr)	2005-11-09	Concentré phytosanitaire émulsifiable contenant des agents anti-moussants
US6387848B1 (en)	2002-05-14	Non-aqueous concentrated spreading oil composition
EP1023833A2 (fr)	2000-08-02	Concenté émulsifiable contenant un ou plusieurs pesticides et adjvants
AU2022301619B2 (en)	2024-03-28	A solid bio-pesticidal composition comprising of elemental sulphur and azadirachtin
MXPA01003037A (en)	2003-11-07	Non-aqueous suspension concentrate
EP0878128A1 (fr)	1998-11-18	Formulations solides