ZA200102411B - Non-aqueous suspension concentrate. - Google Patents

Non-aqueous suspension concentrate. Download PDF

Info

Publication number: ZA200102411B
Authority: ZA; South Africa
Prior art keywords: accordance; aqueous; suspension concentrate; adjuvant; stable suspension
Prior art date: 1998-09-25

Application number

ZA200102411A

Other languages

English (en)

Inventor

Michael Aven

Original Assignee

American Cyanamid Co

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

2001-03-23

Publication date

2002-03-25

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=ZA200102411(B) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.

2001-03-23 Application filed by American Cyanamid Co filed Critical American Cyanamid Co

2002-03-25 Publication of ZA200102411B publication Critical patent/ZA200102411B/en

Links

239000007900 aqueous suspension Substances 0.000 title description 5
239000012141 concentrate Substances 0.000 title description 5
150000001875 compounds Chemical class 0.000 claims description 51
239000004546 suspension concentrate Substances 0.000 claims description 46
239000000203 mixture Substances 0.000 claims description 44
-1 alkyl lactates Chemical class 0.000 claims description 40
239000002671 adjuvant Substances 0.000 claims description 30
238000009472 formulation Methods 0.000 claims description 24
239000002270 dispersing agent Substances 0.000 claims description 21
229910052784 alkaline earth metal Inorganic materials 0.000 claims description 9
150000001412 amines Chemical class 0.000 claims description 8
125000000129 anionic group Chemical group 0.000 claims description 8
238000000034 method Methods 0.000 claims description 8
239000003960 organic solvent Substances 0.000 claims description 7
125000005843 halogen group Chemical group 0.000 claims description 6
150000003626 triacylglycerols Chemical class 0.000 claims description 6
241000607479 Yersinia pestis Species 0.000 claims description 5
150000001298 alcohols Chemical class 0.000 claims description 5
125000000217 alkyl group Chemical group 0.000 claims description 5
150000002148 esters Chemical class 0.000 claims description 5
238000003801 milling Methods 0.000 claims description 5
239000010773 plant oil Substances 0.000 claims description 5
238000002360 preparation method Methods 0.000 claims description 5
239000002562 thickening agent Substances 0.000 claims description 5
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 5
229920003171 Poly (ethylene oxide) Polymers 0.000 claims description 4
239000003513 alkali Substances 0.000 claims description 4
125000003545 alkoxy 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
125000000623 heterocyclic group Chemical group 0.000 claims description 4
229910052757 nitrogen Inorganic materials 0.000 claims description 4
UFTFJSFQGQCHQW-UHFFFAOYSA-N triformin Chemical compound O=COCC(OC=O)COC=O UFTFJSFQGQCHQW-UHFFFAOYSA-N 0.000 claims description 4
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
125000001188 haloalkyl group Chemical group 0.000 claims description 3
238000002156 mixing Methods 0.000 claims description 3
125000004433 nitrogen atom Chemical group N* 0.000 claims description 3
YWBFPKPWMSWWEA-UHFFFAOYSA-O triazolopyrimidine Chemical compound 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 3
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 2
125000003342 alkenyl 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
125000001072 heteroaryl group Chemical group 0.000 claims description 2
229910052739 hydrogen Inorganic materials 0.000 claims description 2
239000001257 hydrogen Substances 0.000 claims description 2
125000000547 substituted alkyl group Chemical group 0.000 claims description 2
125000003827 glycol group Chemical group 0.000 claims 1
239000004480 active ingredient Substances 0.000 description 17
229920002257 Plurafac® Polymers 0.000 description 12
239000004615 ingredient Substances 0.000 description 12
241000196324 Embryophyta Species 0.000 description 9
239000000126 substance Substances 0.000 description 7
239000003795 chemical substances by application Substances 0.000 description 6
238000010790 dilution Methods 0.000 description 6
239000012895 dilution Substances 0.000 description 6
239000002245 particle Substances 0.000 description 6
239000007921 spray Substances 0.000 description 6
CNPVJWYWYZMPDS-UHFFFAOYSA-N 2-methyldecane Chemical compound CCCCCCCCC(C)C CNPVJWYWYZMPDS-UHFFFAOYSA-N 0.000 description 5
239000002904 solvent Substances 0.000 description 5
239000004094 surface-active agent Substances 0.000 description 5
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 4
MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical class OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 4
150000002191 fatty alcohols Chemical class 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
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 3
241001646398 Pseudomonas chlororaphis Species 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
125000004432 carbon atom Chemical group C* 0.000 description 3
239000004359 castor oil Substances 0.000 description 3
235000019438 castor oil Nutrition 0.000 description 3
239000006185 dispersion Substances 0.000 description 3
230000000694 effects Effects 0.000 description 3
150000002334 glycols Chemical class 0.000 description 3
239000004009 herbicide Substances 0.000 description 3
125000004435 hydrogen atom Chemical group [H]* 0.000 description 3
239000007788 liquid Substances 0.000 description 3
230000000361 pesticidal effect Effects 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
WNZQDUSMALZDQF-UHFFFAOYSA-N 2-benzofuran-1(3H)-one Chemical compound C1=CC=C2C(=O)OCC2=C1 WNZQDUSMALZDQF-UHFFFAOYSA-N 0.000 description 2
241000894006 Bacteria Species 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
PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
241000700605 Viruses Species 0.000 description 2
FPIPGXGPPPQFEQ-OVSJKPMPSA-N all-trans-retinol Chemical compound OC\C=C(/C)\C=C\C=C(/C)\C=C\C1=C(C)CCCC1(C)C FPIPGXGPPPQFEQ-OVSJKPMPSA-N 0.000 description 2
WMGSQTMJHBYJMQ-UHFFFAOYSA-N aluminum;magnesium;silicate Chemical compound [Mg+2].[Al+3].[O-][Si]([O-])([O-])[O-] WMGSQTMJHBYJMQ-UHFFFAOYSA-N 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
230000004071 biological effect Effects 0.000 description 2
229920001400 block copolymer Polymers 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
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
229940117927 ethylene oxide Drugs 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
125000003709 fluoroalkyl group Chemical group 0.000 description 2
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 2
RONFGUROBZGJKP-UHFFFAOYSA-N iminoctadine Chemical compound NC(N)=NCCCCCCCCNCCCCCCCCN=C(N)N RONFGUROBZGJKP-UHFFFAOYSA-N 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
JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-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
125000000962 organic group Chemical group 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
239000005871 repellent Substances 0.000 description 2
230000002940 repellent Effects 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
239000000725 suspension Substances 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
LOQQVLXUKHKNIA-UHFFFAOYSA-N thifensulfuron Chemical compound COC1=NC(C)=NC(NC(=O)NS(=O)(=O)C2=C(SC=C2)C(O)=O)=N1 LOQQVLXUKHKNIA-UHFFFAOYSA-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
SAPGTCDSBGMXCD-UHFFFAOYSA-N (2-chlorophenyl)-(4-fluorophenyl)-pyrimidin-5-ylmethanol Chemical compound C=1N=CN=CC=1C(C=1C(=CC=CC=1)Cl)(O)C1=CC=C(F)C=C1 SAPGTCDSBGMXCD-UHFFFAOYSA-N 0.000 description 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 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
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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
YIKWKLYQRFRGPM-UHFFFAOYSA-N 1-dodecylguanidine acetate Chemical compound CC(O)=O.CCCCCCCCCCCCN=C(N)N YIKWKLYQRFRGPM-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
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YIVXMZJTEQBPQO-UHFFFAOYSA-N 2,4-DB Chemical compound OC(=O)CCCOC1=CC=C(Cl)C=C1Cl YIVXMZJTEQBPQO-UHFFFAOYSA-N 0.000 description 1
OZSVBRVFXIOJSU-UHFFFAOYSA-N 2,6-dichloro-n-[[4-(trifluoromethyl)phenyl]methyl]benzamide Chemical compound C1=CC(C(F)(F)F)=CC=C1CNC(=O)C1=C(Cl)C=CC=C1Cl OZSVBRVFXIOJSU-UHFFFAOYSA-N 0.000 description 1
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YTOPFCCWCSOHFV-UHFFFAOYSA-N 2,6-dimethyl-4-tridecylmorpholine Chemical compound CCCCCCCCCCCCCN1CC(C)OC(C)C1 YTOPFCCWCSOHFV-UHFFFAOYSA-N 0.000 description 1
MZHCENGPTKEIGP-UHFFFAOYSA-N 2-(2,4-dichlorophenoxy)propanoic acid Chemical compound OC(=O)C(C)OC1=CC=C(Cl)C=C1Cl MZHCENGPTKEIGP-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
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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
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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)
Catching Or Destruction (AREA)
Saccharide Compounds (AREA)

ZA200102411A 1998-09-25 2001-03-23 Non-aqueous suspension concentrate. ZA200102411B (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US16085698A	1998-09-25	1998-09-25

Publications (1)

Publication Number	Publication Date
ZA200102411B true ZA200102411B (en)	2002-03-25

Family

ID=22578753

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
ZA200102411A ZA200102411B (en)	1998-09-25	2001-03-23	Non-aqueous suspension concentrate.

Country Status (22)

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

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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
ES2223932T3 (es) *	2000-08-25	2005-03-01	Basf Aktiengesellschaft	Formulacion fungicida.
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
WO2004008855A1 (de) *	2002-07-18	2004-01-29	Basf Aktiengesellschaft	Fungizide mischungen
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
ES2308256T3 (es)	2003-09-24	2008-12-01	Wyeth Holdings Corporation	6-aril-7-halo-imidazo(1,2-a)pirimidinas como agentes anticancerosos.
SI1680425T1 (sl)	2003-09-24	2007-04-30	Wyeth Corp	6-((substituirani)fenil)triazolopirimidini kot sredstva proti raku
WO2005074685A1 (en) *	2004-02-06	2005-08-18	Bayer Cropscience Gmbh	Plant protection compositions and use thereof
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
AU2006274070C1 (en) *	2005-07-27	2012-03-29	Basf Se	Fungicidal mixtures based on azolopyrimidinylamines
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
EP1905300A1 (de) *	2006-09-30	2008-04-02	Bayer CropScience AG	Wasser dispergierbare agrochemische Formulierungen enthaltend Polyalkoxytriglyzeride als Penetrationsförderer
MX2009003378A (es) *	2006-09-30	2009-04-09	Bayer Cropscience Ag	Concentrados en suspension para la mejora de la absorcion por la raiz de principios activos agroquimicos.
EP1905302A1 (de) *	2006-09-30	2008-04-02	Bayer CropScience AG	Suspensionskonzentrate
WO2009118025A1 (en) *	2008-03-27	2009-10-01	Bayer Cropscience Aktiengesellschaft	Method for controlling animal pest and plant pathogenic fungi by applying an agrochemical composition into the culture medium, suitable formulation and use thereof
WO2009118027A1 (en) *	2008-03-27	2009-10-01	Bayer Cropscience Aktiengesellschaft	Suspension concentrates for improving root uptake of agrochemically active compounds
EP2326169B1 (en)	2008-05-28	2016-07-27	GAT Microencapsulation GmbH	Suspension concentrates in oil of sulfonylureas and combinations with fluroxypyr or other agrochemicals
HUE036088T2 (hu) *	2010-02-12	2018-06-28	Basf Se	Oldott és szuszpendált peszticidet, alkil-laktátot és alkoholt tartalmazó vízmentes készítmény
CN103118536B (zh) *	2010-04-26	2015-07-01	陶氏益农公司	经稳定化的农业油分散体
DK2736327T3 (da)	2011-07-26	2018-04-23	Clariant Int Ltd	Æteriserede lactatestere, fremgangsmåde til fremstilling af disse og deres anvendelse til forbedring af virkningen af plantebeskyttelsesmidler
BR112014022648B1 (pt) *	2012-03-13	2021-05-25	Basf Se	formulação de concentrado líquido, preparação aquosa, métodos para proteger plantas, não-terapêutico para controlar pragas invertebradas e para proteção de material de propagação de planta contra pragas invertebradas, e usos de uma formulação
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
CZ288224B6 (en) *	1993-09-28	2001-05-16	American Cyanamid Co	Herbicidal emulsifiable compositions formed by suspension concentrate
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 JP JP2000571755A patent/JP2002525291A/ja not_active Withdrawn
- 1999-09-22 DE DE69914364T patent/DE69914364T2/de not_active Revoked
- 1999-09-22 IL IL14208499A patent/IL142084A/xx not_active IP Right Cessation
- 1999-09-22 AU AU62601/99A patent/AU765664B2/en not_active Ceased
- 1999-09-22 SK SK366-2001A patent/SK3662001A3/sk unknown
- 1999-09-22 ES ES99949806T patent/ES2214890T3/es not_active Expired - Lifetime
- 1999-09-22 PT PT99949806T patent/PT1130962E/pt unknown
- 1999-09-22 CN CN998114057A patent/CN1215764C/zh not_active Expired - Fee Related
- 1999-09-22 CZ CZ20011057A patent/CZ20011057A3/cs unknown
- 1999-09-22 BR BR9913922-7A patent/BR9913922A/pt not_active Application Discontinuation
- 1999-09-22 PL PL99346870A patent/PL346870A1/xx not_active IP Right Cessation
- 1999-09-22 UA UA2001042823A patent/UA70965C2/uk unknown
- 1999-09-22 RU RU2001111328/12A patent/RU2224434C2/ru not_active IP Right Cessation
- 1999-09-22 AT AT99949806T patent/ATE258009T1/de not_active IP Right Cessation
- 1999-09-22 HU HU0103741A patent/HUP0103741A3/hu unknown
- 1999-09-22 EP EP99949806A patent/EP1130962B1/en not_active Revoked
- 1999-09-22 NZ NZ510741A patent/NZ510741A/en unknown
- 1999-09-22 CA CA002345296A patent/CA2345296A1/en not_active Abandoned
- 1999-09-22 KR KR1020017003789A patent/KR100689910B1/ko not_active Expired - Fee Related
- 1999-09-22 WO PCT/US1999/022046 patent/WO2000018227A1/en not_active Ceased
- 1999-09-22 DK DK99949806T patent/DK1130962T3/da active
2001
- 2001-03-23 ZA ZA200102411A patent/ZA200102411B/en unknown

Also Published As

Publication number	Publication date
NZ510741A (en)	2003-08-29
CN1320015A (zh)	2001-10-31
ES2214890T3 (es)	2004-09-16
PT1130962E (pt)	2004-04-30
CA2345296A1 (en)	2000-04-06
DE69914364T2 (de)	2004-07-22
AU765664B2 (en)	2003-09-25
AU6260199A (en)	2000-04-17
KR20010106488A (ko)	2001-11-29
CN1215764C (zh)	2005-08-24
IL142084A (en)	2005-12-18
RU2224434C2 (ru)	2004-02-27
WO2000018227A1 (en)	2000-04-06
UA70965C2 (uk)	2004-11-15
DE69914364D1 (de)	2004-02-26
JP2002525291A (ja)	2002-08-13
HUP0103741A2 (hu)	2002-01-28
DK1130962T3 (da)	2004-05-17
ATE258009T1 (de)	2004-02-15
BR9913922A (pt)	2002-04-23
HUP0103741A3 (en)	2004-09-28
IL142084A0 (en)	2002-03-10
CZ20011057A3 (cs)	2002-05-15
PL346870A1 (en)	2002-03-11
SK3662001A3 (en)	2001-11-06
EP1130962A1 (en)	2001-09-12
KR100689910B1 (ko)	2007-03-09
EP1130962B1 (en)	2004-01-21

Publication	Publication Date	Title
AU765664B2 (en)	2003-09-25	Non-aqueous suspension concentrate
US6165940A (en)	2000-12-26	Non-aqueous suspension concentrate
US6383984B1 (en)	2002-05-07	Aqueous suspension concentrate
EP2912945B1 (en)	2018-10-10	Suspension concentrate comprising tebuconazole
EP1023832A1 (en)	2000-08-02	Aqueous suspension concentrate
EP0933025B1 (en)	2004-08-04	Emulsifiable concentrate containing one or more pesticides
US6566308B1 (en)	2003-05-20	Emulsifiable concentrate containing one or more pesticides and adjuvants
CN115087349A (zh)	2022-09-20	用于农业产品的表面活性剂
CN1107273A (zh)	1995-08-23	改进的农业用制剂
EP1025757B1 (en)	2005-11-09	Crop protection emulsifiable concentrate containing defoaming agents
US6387848B1 (en)	2002-05-14	Non-aqueous concentrated spreading oil composition
US6444618B1 (en)	2002-09-03	Crop protection emulsifiable concentrate containing defoaming agents
EP1023833A2 (en)	2000-08-02	Emulsifiable concentrate containing one or more pesticides and adjuvants
US6030924A (en)	2000-02-29	Solid formulations
AU740169B2 (en)	2001-11-01	Solid formulations for crop protection
MXPA01003037A (en)	2003-11-07	Non-aqueous suspension concentrate
TWI236872B (en)	2005-08-01	Non-aqueous concentrated spreading oil composition
JP2005536544A (ja)	2005-12-02	組成物