AR071343A1 - Composicion para la salud de plantas - Google Patents
Composicion para la salud de plantasInfo
- Publication number
- AR071343A1 AR071343A1 ARP090100378A AR071343A1 AR 071343 A1 AR071343 A1 AR 071343A1 AR P090100378 A ARP090100378 A AR P090100378A AR 071343 A1 AR071343 A1 AR 071343A1
- Authority
- AR
- Argentina
- Prior art keywords
- compound
- plants
- plant
- fungicide
- health
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title abstract 4
- -1 amide compound Chemical class 0.000 abstract 15
- 230000000855 fungicidal effect Effects 0.000 abstract 6
- 239000000417 fungicide Substances 0.000 abstract 6
- 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 abstract 3
- 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 abstract 3
- 239000005767 Epoxiconazole Substances 0.000 abstract 3
- 239000005868 Metconazole Substances 0.000 abstract 3
- 239000005822 Propiconazole Substances 0.000 abstract 3
- 239000005839 Tebuconazole Substances 0.000 abstract 3
- 229940125782 compound 2 Drugs 0.000 abstract 3
- 150000001875 compounds Chemical class 0.000 abstract 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 abstract 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 3
- STJLVHWMYQXCPB-UHFFFAOYSA-N propiconazole Chemical compound O1C(CCC)COC1(C=1C(=CC(Cl)=CC=1)Cl)CN1N=CN=C1 STJLVHWMYQXCPB-UHFFFAOYSA-N 0.000 abstract 3
- 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 abstract 2
- 239000005730 Azoxystrobin Substances 0.000 abstract 2
- 239000005785 Fluquinconazole Substances 0.000 abstract 2
- 239000005787 Flutriafol Substances 0.000 abstract 2
- 239000005562 Glyphosate Substances 0.000 abstract 2
- 239000005796 Ipconazole Substances 0.000 abstract 2
- 239000005820 Prochloraz Substances 0.000 abstract 2
- 229930182692 Strobilurin Natural products 0.000 abstract 2
- 239000005847 Triazoxide Substances 0.000 abstract 2
- 239000005857 Trifloxystrobin Substances 0.000 abstract 2
- SRVFFFJZQVENJC-IHRRRGAJSA-N aloxistatin Chemical compound CCOC(=O)[C@H]1O[C@@H]1C(=O)N[C@@H](CC(C)C)C(=O)NCCC(C)C SRVFFFJZQVENJC-IHRRRGAJSA-N 0.000 abstract 2
- 150000001408 amides Chemical class 0.000 abstract 2
- 150000003851 azoles Chemical class 0.000 abstract 2
- WFDXOXNFNRHQEC-GHRIWEEISA-N azoxystrobin Chemical compound CO\C=C(\C(=O)OC)C1=CC=CC=C1OC1=CC(OC=2C(=CC=CC=2)C#N)=NC=N1 WFDXOXNFNRHQEC-GHRIWEEISA-N 0.000 abstract 2
- 229940126214 compound 3 Drugs 0.000 abstract 2
- 229910052731 fluorine Chemical group 0.000 abstract 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 abstract 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 abstract 2
- XDDAORKBJWWYJS-UHFFFAOYSA-N glyphosate Chemical compound OC(=O)CNCP(O)(O)=O XDDAORKBJWWYJS-UHFFFAOYSA-N 0.000 abstract 2
- 229940097068 glyphosate Drugs 0.000 abstract 2
- 230000002363 herbicidal effect Effects 0.000 abstract 2
- 239000004009 herbicide Substances 0.000 abstract 2
- 239000002917 insecticide Substances 0.000 abstract 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 abstract 2
- TVLSRXXIMLFWEO-UHFFFAOYSA-N prochloraz Chemical compound C1=CN=CN1C(=O)N(CCC)CCOC1=C(Cl)C=C(Cl)C=C1Cl TVLSRXXIMLFWEO-UHFFFAOYSA-N 0.000 abstract 2
- WZZLDXDUQPOXNW-UHFFFAOYSA-N propamocarb Chemical compound CCCOC(=O)NCCCN(C)C WZZLDXDUQPOXNW-UHFFFAOYSA-N 0.000 abstract 2
- IQGKIPDJXCAMSM-UHFFFAOYSA-N triazoxide Chemical compound N=1C2=CC=C(Cl)C=C2[N+]([O-])=NC=1N1C=CN=C1 IQGKIPDJXCAMSM-UHFFFAOYSA-N 0.000 abstract 2
- 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 abstract 2
- 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 abstract 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 abstract 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 abstract 1
- KWLVWJPJKJMCSH-UHFFFAOYSA-N 2-(4-chlorophenyl)-N-{2-[3-methoxy-4-(prop-2-yn-1-yloxy)phenyl]ethyl}-2-(prop-2-yn-1-yloxy)acetamide Chemical compound C1=C(OCC#C)C(OC)=CC(CCNC(=O)C(OCC#C)C=2C=CC(Cl)=CC=2)=C1 KWLVWJPJKJMCSH-UHFFFAOYSA-N 0.000 abstract 1
- SOUGWDPPRBKJEX-UHFFFAOYSA-N 3,5-dichloro-N-(1-chloro-3-methyl-2-oxopentan-3-yl)-4-methylbenzamide Chemical compound ClCC(=O)C(C)(CC)NC(=O)C1=CC(Cl)=C(C)C(Cl)=C1 SOUGWDPPRBKJEX-UHFFFAOYSA-N 0.000 abstract 1
- ZOCSXAVNDGMNBV-UHFFFAOYSA-N 5-amino-1-[2,6-dichloro-4-(trifluoromethyl)phenyl]-4-[(trifluoromethyl)sulfinyl]-1H-pyrazole-3-carbonitrile Chemical compound NC1=C(S(=O)C(F)(F)F)C(C#N)=NN1C1=C(Cl)C=C(C(F)(F)F)C=C1Cl ZOCSXAVNDGMNBV-UHFFFAOYSA-N 0.000 abstract 1
- PCCSBWNGDMYFCW-UHFFFAOYSA-N 5-methyl-5-(4-phenoxyphenyl)-3-(phenylamino)-1,3-oxazolidine-2,4-dione Chemical compound O=C1C(C)(C=2C=CC(OC=3C=CC=CC=3)=CC=2)OC(=O)N1NC1=CC=CC=C1 PCCSBWNGDMYFCW-UHFFFAOYSA-N 0.000 abstract 1
- 239000005964 Acibenzolar-S-methyl Substances 0.000 abstract 1
- JJLJMEJHUUYSSY-UHFFFAOYSA-L Copper hydroxide Chemical compound [OH-].[OH-].[Cu+2] JJLJMEJHUUYSSY-UHFFFAOYSA-L 0.000 abstract 1
- 239000005750 Copper hydroxide Substances 0.000 abstract 1
- 239000005752 Copper oxychloride Substances 0.000 abstract 1
- 239000005756 Cymoxanil Substances 0.000 abstract 1
- 239000005762 Dimoxystrobin Substances 0.000 abstract 1
- FNELVJVBIYMIMC-UHFFFAOYSA-N Ethiprole Chemical compound N1=C(C#N)C(S(=O)CC)=C(N)N1C1=C(Cl)C=C(C(F)(F)F)C=C1Cl FNELVJVBIYMIMC-UHFFFAOYSA-N 0.000 abstract 1
- 239000005772 Famoxadone Substances 0.000 abstract 1
- 239000005778 Fenpropimorph Substances 0.000 abstract 1
- 239000005899 Fipronil Substances 0.000 abstract 1
- 239000005780 Fluazinam Substances 0.000 abstract 1
- 239000005782 Fluopicolide Substances 0.000 abstract 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical group FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 abstract 1
- 239000005867 Iprodione Substances 0.000 abstract 1
- 239000005797 Iprovalicarb Substances 0.000 abstract 1
- 239000005800 Kresoxim-methyl Substances 0.000 abstract 1
- NWUWYYSKZYIQAE-ZBFHGGJFSA-N L-(R)-iprovalicarb Chemical compound CC(C)OC(=O)N[C@@H](C(C)C)C(=O)N[C@H](C)C1=CC=C(C)C=C1 NWUWYYSKZYIQAE-ZBFHGGJFSA-N 0.000 abstract 1
- 239000005802 Mancozeb Substances 0.000 abstract 1
- 239000005807 Metalaxyl Substances 0.000 abstract 1
- 239000005809 Metiram Substances 0.000 abstract 1
- 239000005810 Metrafenone Substances 0.000 abstract 1
- 239000005818 Picoxystrobin Substances 0.000 abstract 1
- 239000005821 Propamocarb Substances 0.000 abstract 1
- 239000005823 Propineb Substances 0.000 abstract 1
- 239000005828 Pyrimethanil Substances 0.000 abstract 1
- 239000005837 Spiroxamine Substances 0.000 abstract 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 abstract 1
- 239000005842 Thiophanate-methyl Substances 0.000 abstract 1
- 239000005860 Valifenalate Substances 0.000 abstract 1
- 239000005863 Zoxamide Substances 0.000 abstract 1
- UELITFHSCLAHKR-UHFFFAOYSA-N acibenzolar-S-methyl Chemical group CSC(=O)C1=CC=CC2=C1SN=N2 UELITFHSCLAHKR-UHFFFAOYSA-N 0.000 abstract 1
- 239000004480 active ingredient Substances 0.000 abstract 1
- IMHBYKMAHXWHRP-UHFFFAOYSA-N anilazine Chemical compound ClC1=CC=CC=C1NC1=NC(Cl)=NC(Cl)=N1 IMHBYKMAHXWHRP-UHFFFAOYSA-N 0.000 abstract 1
- OIPMQULDKWSNGX-UHFFFAOYSA-N bis[[ethoxy(oxo)phosphaniumyl]oxy]alumanyloxy-ethoxy-oxophosphanium Chemical compound [Al+3].CCO[P+]([O-])=O.CCO[P+]([O-])=O.CCO[P+]([O-])=O OIPMQULDKWSNGX-UHFFFAOYSA-N 0.000 abstract 1
- JHRWWRDRBPCWTF-OLQVQODUSA-N captafol Chemical compound C1C=CC[C@H]2C(=O)N(SC(Cl)(Cl)C(Cl)Cl)C(=O)[C@H]21 JHRWWRDRBPCWTF-OLQVQODUSA-N 0.000 abstract 1
- 150000004657 carbamic acid derivatives Chemical class 0.000 abstract 1
- RXDMAYSSBPYBFW-PKFCDNJMSA-N carpropamide Chemical compound N([C@@H](C)C=1C=CC(Cl)=CC=1)C(=O)[C@@]1(CC)[C@H](C)C1(Cl)Cl RXDMAYSSBPYBFW-PKFCDNJMSA-N 0.000 abstract 1
- HKMOPYJWSFRURD-UHFFFAOYSA-N chloro hypochlorite;copper Chemical compound [Cu].ClOCl HKMOPYJWSFRURD-UHFFFAOYSA-N 0.000 abstract 1
- 229940125904 compound 1 Drugs 0.000 abstract 1
- 229910001956 copper hydroxide Inorganic materials 0.000 abstract 1
- OPQARKPSCNTWTJ-UHFFFAOYSA-L copper(ii) acetate Chemical compound [Cu+2].CC([O-])=O.CC([O-])=O OPQARKPSCNTWTJ-UHFFFAOYSA-L 0.000 abstract 1
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 abstract 1
- 125000004980 cyclopropylene group Chemical group 0.000 abstract 1
- 125000001028 difluoromethyl group Chemical group [H]C(F)(F)* 0.000 abstract 1
- WXUZAHCNPWONDH-DYTRJAOYSA-N dimoxystrobin Chemical compound CNC(=O)C(=N\OC)\C1=CC=CC=C1COC1=CC(C)=CC=C1C WXUZAHCNPWONDH-DYTRJAOYSA-N 0.000 abstract 1
- PYZSVQVRHDXQSL-UHFFFAOYSA-N dithianon Chemical compound S1C(C#N)=C(C#N)SC2=C1C(=O)C1=CC=CC=C1C2=O PYZSVQVRHDXQSL-UHFFFAOYSA-N 0.000 abstract 1
- 239000012990 dithiocarbamate Substances 0.000 abstract 1
- 150000004659 dithiocarbamates Chemical class 0.000 abstract 1
- VDLGAVXLJYLFDH-UHFFFAOYSA-N fenhexamid Chemical compound C=1C=C(O)C(Cl)=C(Cl)C=1NC(=O)C1(C)CCCCC1 VDLGAVXLJYLFDH-UHFFFAOYSA-N 0.000 abstract 1
- 229940013764 fipronil Drugs 0.000 abstract 1
- UZCGKGPEKUCDTF-UHFFFAOYSA-N fluazinam Chemical compound [O-][N+](=O)C1=CC(C(F)(F)F)=C(Cl)C([N+]([O-])=O)=C1NC1=NC=C(C(F)(F)F)C=C1Cl UZCGKGPEKUCDTF-UHFFFAOYSA-N 0.000 abstract 1
- GBOYJIHYACSLGN-UHFFFAOYSA-N fluopicolide Chemical compound ClC1=CC(C(F)(F)F)=CN=C1CNC(=O)C1=C(Cl)C=CC=C1Cl GBOYJIHYACSLGN-UHFFFAOYSA-N 0.000 abstract 1
- 239000011737 fluorine Chemical group 0.000 abstract 1
- 125000001153 fluoro group Chemical group F* 0.000 abstract 1
- GNVDAZSPJWCIQZ-UHFFFAOYSA-N flusulfamide Chemical compound ClC1=CC([N+](=O)[O-])=CC=C1NS(=O)(=O)C1=CC=C(Cl)C(C(F)(F)F)=C1 GNVDAZSPJWCIQZ-UHFFFAOYSA-N 0.000 abstract 1
- 125000005843 halogen group Chemical group 0.000 abstract 1
- 150000002391 heterocyclic compounds Chemical class 0.000 abstract 1
- 229910052739 hydrogen Inorganic materials 0.000 abstract 1
- 239000001257 hydrogen Substances 0.000 abstract 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 1
- RONFGUROBZGJKP-UHFFFAOYSA-N iminoctadine Chemical compound NC(N)=NCCCCCCCCNCCCCCCCCN=C(N)N RONFGUROBZGJKP-UHFFFAOYSA-N 0.000 abstract 1
- ONUFESLQCSAYKA-UHFFFAOYSA-N iprodione Chemical compound O=C1N(C(=O)NC(C)C)CC(=O)N1C1=CC(Cl)=CC(Cl)=C1 ONUFESLQCSAYKA-UHFFFAOYSA-N 0.000 abstract 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 abstract 1
- 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 abstract 1
- YKSNLCVSTHTHJA-UHFFFAOYSA-L maneb Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S YKSNLCVSTHTHJA-UHFFFAOYSA-L 0.000 abstract 1
- 229920000940 maneb Polymers 0.000 abstract 1
- ZQEIXNIJLIKNTD-UHFFFAOYSA-N methyl N-(2,6-dimethylphenyl)-N-(methoxyacetyl)alaninate Chemical compound COCC(=O)N(C(C)C(=O)OC)C1=C(C)C=CC=C1C ZQEIXNIJLIKNTD-UHFFFAOYSA-N 0.000 abstract 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 1
- 229920000257 metiram Polymers 0.000 abstract 1
- HIIRDDUVRXCDBN-OBGWFSINSA-N metominostrobin Chemical compound CNC(=O)C(=N\OC)\C1=CC=CC=C1OC1=CC=CC=C1 HIIRDDUVRXCDBN-OBGWFSINSA-N 0.000 abstract 1
- 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 abstract 1
- UMRZSTCPUPJPOJ-UHFFFAOYSA-N norbornane Chemical group C1CC2CCC1C2 UMRZSTCPUPJPOJ-UHFFFAOYSA-N 0.000 abstract 1
- 150000004045 organic chlorine compounds Chemical class 0.000 abstract 1
- IBSNKSODLGJUMQ-SDNWHVSQSA-N picoxystrobin Chemical compound CO\C=C(\C(=O)OC)C1=CC=CC=C1COC1=CC=CC(C(F)(F)F)=N1 IBSNKSODLGJUMQ-SDNWHVSQSA-N 0.000 abstract 1
- KKMLIVYBGSAJPM-UHFFFAOYSA-L propineb Chemical compound [Zn+2].[S-]C(=S)NC(C)CNC([S-])=S KKMLIVYBGSAJPM-UHFFFAOYSA-L 0.000 abstract 1
- ZLIBICFPKPWGIZ-UHFFFAOYSA-N pyrimethanil Chemical compound CC1=CC(C)=NC(NC=2C=CC=CC=2)=N1 ZLIBICFPKPWGIZ-UHFFFAOYSA-N 0.000 abstract 1
- PUYXTUJWRLOUCW-UHFFFAOYSA-N spiroxamine Chemical compound O1C(CN(CC)CCC)COC11CCC(C(C)(C)C)CC1 PUYXTUJWRLOUCW-UHFFFAOYSA-N 0.000 abstract 1
- 125000001424 substituent group Chemical group 0.000 abstract 1
- 229910052717 sulfur Inorganic materials 0.000 abstract 1
- 239000011593 sulfur Substances 0.000 abstract 1
- LITQZINTSYBKIU-UHFFFAOYSA-F tetracopper;hexahydroxide;sulfate Chemical compound [OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[Cu+2].[Cu+2].[Cu+2].[Cu+2].[O-]S([O-])(=O)=O LITQZINTSYBKIU-UHFFFAOYSA-F 0.000 abstract 1
- 125000001544 thienyl group Chemical group 0.000 abstract 1
- QGHREAKMXXNCOA-UHFFFAOYSA-N thiophanate-methyl Chemical group COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC QGHREAKMXXNCOA-UHFFFAOYSA-N 0.000 abstract 1
- HYVWIQDYBVKITD-UHFFFAOYSA-N tolylfluanid Chemical compound CN(C)S(=O)(=O)N(SC(F)(Cl)Cl)C1=CC=C(C)C=C1 HYVWIQDYBVKITD-UHFFFAOYSA-N 0.000 abstract 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 abstract 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 abstract 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
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/56—1,2-Diazoles; Hydrogenated 1,2-diazoles
-
- 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
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E50/00—Technologies for the production of fuel of non-fossil origin
- Y02E50/30—Fuel from waste, e.g. synthetic alcohol or diesel
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02W—CLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO WASTEWATER TREATMENT OR WASTE MANAGEMENT
- Y02W30/00—Technologies for solid waste management
- Y02W30/40—Bio-organic fraction processing; Production of fertilisers from the organic fraction of waste or refuse
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Cultivation Of Plants (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Método para mejorar la salud de plantas de al menos una variedad de plantas, donde el método comprende tratar la planta y/o el lugar donde está creciendo o intenta crecer la planta con un compuesto amida de la formula 1. La presente también se refiere a un método para mejorar la salud de plantas de al menos una variedad de plantas, donde el método comprende tratar la planta y/o el lugar donde está creciendo o intenta crecer la planta con una mezcla que comprende un compuesto amida que presenta la formula 1 y al menos un compuesto seleccionado del grupo que consiste de otro fungicida 2 (compuesto 2), otro fungicida 3 (compuesto 2b), un insecticida (compuesto 3) y un herbicida (compuesto 4). Reivindicacion 1: Un método para mejorar la salud de plantas de al menos una variedad de plantas, caracterizado porque el método comprende tratar la planta y/o el lugar donde está creciendo o intenta crecer la planta con una amida que presenta la formula 1 en la que los sustituyentes son como se definen a continuacion: R4 es metilo, difluorometilo, o trifluorometilo; R5 es hidrogeno o fluor; M es un anillo tienilo o es un anillo fenilo, donde el anillo fenilo esta sustituido o no sustituido con un átomo de fluor; Q es un enlace directo, un anillo ciclopropileno o un anillo biciclo[2,2,1]heptano alineado; R1 es ciclopropilo, 1,3-dimetilbutilo, isopropilo, fenilo sustituido con dos o tres átomos de halogeno o un radical trifluorometiltio. Reivindicacion 4: El método como se reivindica en cualquiera de las reivindicaciones 1 a 3, caracterizado porque una mezcla del compuesto amida de formula 1 (compuesto 1) y otro fungicida 2 (compuesto 2) es aplicada en cantidades sinergísticamente efectivas para la salud de las plantas, donde el otro fungicida 2 es seleccionado del grupo que consiste de (i) estrobilurinas, seleccionadas de azoxiestrobina, dimoxiestrobina, fluoxaestrobina, kresoxim-metilo, metominoestrobina, orisaestrobina, picoxiestrobina, piracloestrobina y trifloxiestrobina; (ii) amidas carboxílicas, seleccionadas de boscalida, fenhexamida, metalaxilo, dimetomorf, fluopicolida (picobenzamida), zoxamida, mandipropamida y carpropamida; (iii) azoles, seleccionados de ciproconazol, difenoconazol, epoxiconazol, flusilazol, fluquinconazol, flutriafol, ipconazol, metconazol, propiconazol, protioconazol, tebuconazol, ciazofamida, prochloraz, etaboxam y triazoxido; (iv) compuestos heterocíclicos, seleccionadas de famoxadona, fluazinam, ciprodinilo, pirimetanilo, fenpropimorf, iprodiona, acibenzolar-S-metilo, proquinazida, quinoxifeno, fenpiclonilo, captano, fenpropidino, captafol y anilazina; (v) carbamatos y ditiocarbamatos, seleccionadas de mancozeb, metiram, iprovalicarb, maneb, propineb, flubentiavalicarb (bentiavalicarb) y propamocarb (vi) compuestos organo-cloro, seleccionados de tiofanato metilo, clorotalonilo, tolilfluanida y flusulfamida; (vii) ingredientes activos inorgánicos, seleccionadas de la composicion Bordeaux, acetato de cobre, hidroxido de cobre, oxicloruro de cobre, sulfato de cobre básico y azufre; (viii) varios, seleccionados de espiroxamina, guazatina, cimoxanilo, ciflufenamida, valifenal, metrafenona, fosetil-aluminio y ditianona. Reivindicacion 6: El método como se reivindica en la reivindicacion 4, caracterizado porque el otro fungicida 2 (compuesto 2) es seleccionado del grupo que consiste de (i) estrobilurinas, seleccionadas de azoxiestrobina, orisaestrobina, piracloestrobina y trifloxiestrobina; (iii) azoles, seleccionados de epoxiconazol, metconazol, protioconazol, tebuconazol y propiconazol. Reivindicacion 9: El método como se reivindica en cualquiera de las reivindicaciones 1 a 3, caracterizado porque comprende adicionalmente un insecticida (compuesto 3), seleccionado de fipronilo y etiprol. Reivindicacion 10: El método como se reivindica en cualquiera de las reivindicaciones 1 a 9, caracterizado porque comprende adicionalmente otro fungicida 3 (compuesto 2b), seleccionado de ciproconazol, difenoconazol, epoxiconazol, flusilazol, fluquinconazol, flutriafol, ipconazol, metconazol, propiconazol, protioconazol, tebuconazol, ciazofamida, prochloraz, etaboxam y triazoxido. Reivindicacion 11: El método como se reivindica en cualquiera de las reivindicaciones 1 a 9, caracterizado porque comprende adicionalmente un herbicida (compuesto 4) seleccionado de glifosato, sulfosinato y glifosinato.
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|---|---|---|---|
| PCT/EP2008/051375 WO2008095913A2 (en) | 2007-02-06 | 2008-02-05 | Pesticidal mixtures |
| EP08161625 | 2008-08-01 |
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| AR071343A1 true AR071343A1 (es) | 2010-06-16 |
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| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP090100378 AR071343A1 (es) | 2008-02-05 | 2009-02-04 | Composicion para la salud de plantas |
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| UA (1) | UA105897C2 (es) |
| WO (1) | WO2009098218A2 (es) |
| ZA (1) | ZA201006292B (es) |
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| CN101674729A (zh) * | 2007-03-20 | 2010-03-17 | 巴斯夫欧洲公司 | 保护大豆以防真菌侵染的方法 |
| BRPI0905841A2 (pt) * | 2008-02-05 | 2015-06-30 | Basf Se | "método para melhorar a saúde de uma planta, uso de uma amida, misturas fungicidas, método para controlar pragas e semente" |
| EP2105049A1 (en) * | 2008-03-28 | 2009-09-30 | Bayer CropScience AG | Method of plant growth promotion using amide compounds |
| US20110203018A1 (en) * | 2008-10-21 | 2011-08-18 | Basf Se | Use of Carboxamides on Cultivated Plants |
-
2009
- 2009-02-04 UA UAA201010580A patent/UA105897C2/uk unknown
- 2009-02-04 KR KR1020107019685A patent/KR20100110892A/ko not_active Withdrawn
- 2009-02-04 AU AU2009211411A patent/AU2009211411A1/en not_active Abandoned
- 2009-02-04 AR ARP090100378 patent/AR071343A1/es unknown
- 2009-02-04 JP JP2010545452A patent/JP2011511032A/ja active Pending
- 2009-02-04 CN CN200980108215.2A patent/CN101965128B/zh not_active Expired - Fee Related
- 2009-02-04 EA EA201001232A patent/EA018987B1/ru not_active IP Right Cessation
- 2009-02-04 CA CA 2712488 patent/CA2712488A1/en not_active Abandoned
- 2009-02-04 MX MX2010008129A patent/MX2010008129A/es not_active Application Discontinuation
- 2009-02-04 US US12/865,784 patent/US20110263423A1/en not_active Abandoned
- 2009-02-04 BR BRPI0905941-5A patent/BRPI0905941A2/pt not_active Application Discontinuation
- 2009-02-04 EP EP20090709231 patent/EP2242366A2/en not_active Withdrawn
- 2009-02-04 WO PCT/EP2009/051241 patent/WO2009098218A2/en not_active Ceased
- 2009-02-05 PE PE2009000182A patent/PE20091459A1/es not_active Application Discontinuation
- 2009-02-05 TW TW98103740A patent/TWI457326B/zh not_active IP Right Cessation
-
2010
- 2010-07-29 CR CR11611A patent/CR11611A/es unknown
- 2010-09-02 ZA ZA2010/06292A patent/ZA201006292B/en unknown
- 2010-09-02 CO CO10108742A patent/CO6300902A2/es not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| AU2009211411A1 (en) | 2009-08-13 |
| UA105897C2 (uk) | 2014-07-10 |
| BRPI0905941A2 (pt) | 2015-06-30 |
| EA018987B1 (ru) | 2013-12-30 |
| EA201001232A1 (ru) | 2011-04-29 |
| EP2242366A2 (en) | 2010-10-27 |
| MX2010008129A (es) | 2010-08-11 |
| CA2712488A1 (en) | 2009-08-13 |
| CR11611A (es) | 2010-11-23 |
| CN101965128B (zh) | 2014-10-01 |
| TWI457326B (zh) | 2014-10-21 |
| JP2011511032A (ja) | 2011-04-07 |
| US20110263423A1 (en) | 2011-10-27 |
| PE20091459A1 (es) | 2009-10-24 |
| WO2009098218A3 (en) | 2010-09-02 |
| ZA201006292B (en) | 2011-11-30 |
| CN101965128A (zh) | 2011-02-02 |
| TW200940510A (en) | 2009-10-01 |
| KR20100110892A (ko) | 2010-10-13 |
| WO2009098218A2 (en) | 2009-08-13 |
| CO6300902A2 (es) | 2011-07-21 |
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