AR067097A1 - Procedimiento para la reduccion de la fototoxicidad de azoles en plantas dicotiledoneas por adicion de aditivos - Google Patents
Procedimiento para la reduccion de la fototoxicidad de azoles en plantas dicotiledoneas por adicion de aditivosInfo
- Publication number
- AR067097A1 AR067097A1 ARP080102653A ARP080102653A AR067097A1 AR 067097 A1 AR067097 A1 AR 067097A1 AR P080102653 A ARP080102653 A AR P080102653A AR P080102653 A ARP080102653 A AR P080102653A AR 067097 A1 AR067097 A1 AR 067097A1
- Authority
- AR
- Argentina
- Prior art keywords
- sodium
- sulphosuccinate
- sulfosuccinate
- triazole
- formula
- Prior art date
Links
- 239000000654 additive Substances 0.000 title abstract 2
- 206010034972 Photosensitivity reaction Diseases 0.000 title 1
- 150000003851 azoles Chemical class 0.000 title 1
- 208000007578 phototoxic dermatitis Diseases 0.000 title 1
- 231100000018 phototoxicity Toxicity 0.000 title 1
- -1 alkali metal sulphosuccinates Chemical class 0.000 abstract 6
- 239000000417 fungicide Substances 0.000 abstract 5
- 150000003852 triazoles Chemical class 0.000 abstract 4
- ULUAUXLGCMPNKK-UHFFFAOYSA-N Sulfobutanedioic acid Chemical class OC(=O)CC(C(O)=O)S(O)(=O)=O ULUAUXLGCMPNKK-UHFFFAOYSA-N 0.000 abstract 2
- 229910052783 alkali metal Inorganic materials 0.000 abstract 2
- 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 abstract 2
- 230000000855 fungicidal effect Effects 0.000 abstract 2
- 229910052739 hydrogen Inorganic materials 0.000 abstract 2
- 239000001257 hydrogen Substances 0.000 abstract 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 2
- 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 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 abstract 1
- ONBWNNUYXGJKKD-UHFFFAOYSA-N 1,4-bis(2-ethylhexoxy)-1,4-dioxobutane-2-sulfonic acid;sodium Chemical compound [Na].CCCCC(CC)COC(=O)CC(S(O)(=O)=O)C(=O)OCC(CC)CCCC ONBWNNUYXGJKKD-UHFFFAOYSA-N 0.000 abstract 1
- FXZAUBIBKADOBA-UHFFFAOYSA-N 1,4-bis(2-methylpropoxy)-1,4-dioxobutane-2-sulfonic acid;sodium Chemical compound [Na].CC(C)COC(=O)CC(S(O)(=O)=O)C(=O)OCC(C)C FXZAUBIBKADOBA-UHFFFAOYSA-N 0.000 abstract 1
- UTWVENOYOROSRG-UHFFFAOYSA-N 1,4-didodecoxy-1,4-dioxobutane-2-sulfonic acid;sodium Chemical compound [Na].CCCCCCCCCCCCOC(=O)CC(S(O)(=O)=O)C(=O)OCCCCCCCCCCCC UTWVENOYOROSRG-UHFFFAOYSA-N 0.000 abstract 1
- YUCTUWYCFFUCOR-UHFFFAOYSA-N 1,4-dihexoxy-1,4-dioxobutane-2-sulfonic acid;sodium Chemical compound [Na].CCCCCCOC(=O)CC(S(O)(=O)=O)C(=O)OCCCCCC YUCTUWYCFFUCOR-UHFFFAOYSA-N 0.000 abstract 1
- GEBAKLQZHWOTKS-UHFFFAOYSA-N 1,4-dioxo-1,4-di(propan-2-yloxy)butane-2-sulfonic acid;sodium Chemical compound [Na].CC(C)OC(=O)CC(S(O)(=O)=O)C(=O)OC(C)C GEBAKLQZHWOTKS-UHFFFAOYSA-N 0.000 abstract 1
- QQYSPMBMXXCTGQ-UHFFFAOYSA-N 1,4-dioxo-1,4-di(tridecoxy)butane-2-sulfonic acid;sodium Chemical compound [Na].CCCCCCCCCCCCCOC(=O)CC(S(O)(=O)=O)C(=O)OCCCCCCCCCCCCC QQYSPMBMXXCTGQ-UHFFFAOYSA-N 0.000 abstract 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 abstract 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 abstract 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 abstract 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 abstract 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 abstract 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 abstract 1
- 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 abstract 1
- 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 abstract 1
- 239000005741 Bromuconazole Substances 0.000 abstract 1
- 239000005767 Epoxiconazole Substances 0.000 abstract 1
- 239000005775 Fenbuconazole Substances 0.000 abstract 1
- 239000005785 Fluquinconazole Substances 0.000 abstract 1
- 239000005787 Flutriafol Substances 0.000 abstract 1
- 241000233866 Fungi Species 0.000 abstract 1
- 239000005796 Ipconazole Substances 0.000 abstract 1
- 239000005868 Metconazole Substances 0.000 abstract 1
- 239000005813 Penconazole Substances 0.000 abstract 1
- 231100000674 Phytotoxicity Toxicity 0.000 abstract 1
- 239000005822 Propiconazole Substances 0.000 abstract 1
- 239000005839 Tebuconazole Substances 0.000 abstract 1
- 239000005840 Tetraconazole Substances 0.000 abstract 1
- 239000005846 Triadimenol Substances 0.000 abstract 1
- 239000005859 Triticonazole Substances 0.000 abstract 1
- 150000001340 alkali metals Chemical class 0.000 abstract 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 abstract 1
- 150000001342 alkaline earth metals Chemical class 0.000 abstract 1
- 125000003545 alkoxy group Chemical group 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- 125000003118 aryl group Chemical group 0.000 abstract 1
- AKNQMEBLVAMSNZ-UHFFFAOYSA-N azaconazole Chemical compound ClC1=CC(Cl)=CC=C1C1(CN2N=CN=C2)OCCO1 AKNQMEBLVAMSNZ-UHFFFAOYSA-N 0.000 abstract 1
- 229950000294 azaconazole Drugs 0.000 abstract 1
- HJJVPARKXDDIQD-UHFFFAOYSA-N bromuconazole Chemical compound ClC1=CC(Cl)=CC=C1C1(CN2N=CN=C2)OCC(Br)C1 HJJVPARKXDDIQD-UHFFFAOYSA-N 0.000 abstract 1
- 239000003795 chemical substances by application Substances 0.000 abstract 1
- 125000000000 cycloalkoxy group Chemical group 0.000 abstract 1
- YHAIUSTWZPMYGG-UHFFFAOYSA-L disodium;2,2-dioctyl-3-sulfobutanedioate Chemical compound [Na+].[Na+].CCCCCCCCC(C([O-])=O)(C(C([O-])=O)S(O)(=O)=O)CCCCCCCC YHAIUSTWZPMYGG-UHFFFAOYSA-L 0.000 abstract 1
- HETXQHOFMGVMJT-UHFFFAOYSA-L disodium;2-(2-ethylhexyl)-2-sulfobutanedioate Chemical compound [Na+].[Na+].CCCCC(CC)CC(S(O)(=O)=O)(C([O-])=O)CC([O-])=O HETXQHOFMGVMJT-UHFFFAOYSA-L 0.000 abstract 1
- 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 1
- 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 1
- 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 abstract 1
- 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 1
- 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 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 1
- 230000003032 phytopathogenic effect Effects 0.000 abstract 1
- 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 1
- 150000003839 salts Chemical class 0.000 abstract 1
- UELAIMNOXLAYRW-UHFFFAOYSA-M sodium;1,4-dicyclohexyloxy-1,4-dioxobutane-2-sulfonate Chemical compound [Na+].C1CCCCC1OC(=O)C(S(=O)(=O)[O-])CC(=O)OC1CCCCC1 UELAIMNOXLAYRW-UHFFFAOYSA-M 0.000 abstract 1
- UMEWSJNRBXKWKZ-UHFFFAOYSA-M sodium;1,4-dioxo-1,4-dipentoxybutane-2-sulfonate Chemical compound [Na+].CCCCCOC(=O)CC(S([O-])(=O)=O)C(=O)OCCCCC UMEWSJNRBXKWKZ-UHFFFAOYSA-M 0.000 abstract 1
- 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 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
- A01N43/64—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with three nitrogen atoms as the only ring hetero atoms
- A01N43/647—Triazoles; Hydrogenated triazoles
- A01N43/653—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
Landscapes
- Life Sciences & Earth Sciences (AREA)
- 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)
Abstract
Además, la solicitud se refiere a agentes que contienen determinados fungicidas de triazol en combinacion con aditivos, en especial sulfosuccinatos de metal alcalino, así como su uso para el combate de hongos fitopatogenos no deseados. Reivindicacion 1: Procedimiento para la reduccion de la fitotoxicidad de fungicidas de triazol en plantas dicotiledoneas, caracterizado porque se anaden a los agentes fungicidas, que contienen al menos un fungicida de triazol, sulfosuccinatos de la formula general (1) en la que R1 y R2 representan, de modo independiente entre sí, hidroxi, alcoxi o cicloalcoxi o el grupo de formula (2) en el que al menos un radical R1 o R2 no representa hidroxi, R3 representa hidrogeno o metilo, R4 representa hidrogeno, alquilo o arilo, m representa un numero entero de 0 a 100, X representa un metal alcalino, donde n representa 1, o un metal alcalinotérreo, donde n representa 2. Reivindicacion 2: Procedimiento de acuerdo con la reivindicacion 1, caracterizado porque se emplea un sulfosuccinato de la formula (1), seleccionado de diisopropil-sulfosuccinato de sodio, diisobutil-sulfosuccinato de sodio, dipentil-sulfosuccinato de sodio, dihexil-sulfosuccinato de sodio, dioctil-sulfosuccinato de sodio, di(2-etilhexil)-sulfosuccinato de sodio, didodecil-sulfosuccinato de sodio, ditridecil-sulfosuccinato de sodio, diciclohexil-sulfosuccinato de sodio, con preferencia di(2-etilhexil)-sulfosuccinato de sodio. Reivindicacion 4: Procedimiento de acuerdo con una de las reivindicaciones 1, 2 o 3, caracterizado porque se emplea un fungicida de triazol seleccionado de azaconazol, bitertanol, bromuconazol, ciproconazol, difenoconazol, diniconazol, diniconazol-M, epoxiconazol, etaconazol, fenbuconazol, fluquinconazol, flusilazol, flutriafol, hexaconazol, imibenconazol, ipconazol, metconazol, miclobutanilo, penconazol, propiconazol, protioconazol, simeconazol, tebuconazol, tetraconazol, triadimefona, triadimenol, triticonazol, y sus correspondientes sales.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP07110836 | 2007-06-22 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR067097A1 true AR067097A1 (es) | 2009-09-30 |
Family
ID=39789966
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP080102653A AR067097A1 (es) | 2007-06-22 | 2008-06-26 | Procedimiento para la reduccion de la fototoxicidad de azoles en plantas dicotiledoneas por adicion de aditivos |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US20100184816A1 (es) |
| AR (1) | AR067097A1 (es) |
| BR (1) | BRPI0812799A2 (es) |
| CL (1) | CL2008001779A1 (es) |
| TW (1) | TW200911117A (es) |
| WO (1) | WO2009000407A1 (es) |
Families Citing this family (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP2533633B1 (de) * | 2010-02-02 | 2017-02-01 | LANXESS Distribution GmbH | Fungizide mischungen |
| EP2353387A1 (de) * | 2010-02-05 | 2011-08-10 | Bayer CropScience AG | Verwendung von Succinat-Dehydrogenase (SDH)-Inhibitoren in der Behandlung von Pflanzenarten der Familie der Süßgräser |
| JP5764957B2 (ja) * | 2010-03-03 | 2015-08-19 | 住友化学株式会社 | 植物病害防除組成物及び植物病害防除方法 |
| US8876481B2 (en) * | 2011-01-05 | 2014-11-04 | General Electric Company | Turbine airfoil component assembly for use in a gas turbine engine and methods for fabricating same |
| CN102172241B (zh) * | 2011-03-19 | 2014-03-19 | 陕西汤普森生物科技有限公司 | 一种含有吡唑醚菌酯与三唑类的农药组合物 |
| CN103563945A (zh) * | 2012-08-05 | 2014-02-12 | 南京华洲药业有限公司 | 一种含吡唑醚菌酯和丙硫菌唑的杀菌组合物及其应用 |
| GB201301975D0 (en) * | 2013-02-04 | 2013-03-20 | Syngenta Participations Ag | New method for the purpose of safening |
| GB201301979D0 (en) | 2013-02-04 | 2013-03-20 | Syngenta Participations Ag | New composition and use thereof |
| CN103548857B (zh) * | 2013-08-21 | 2017-02-08 | 陕西康禾立丰生物科技药业有限公司 | 一种含吡唑醚菌酯的农药组合物 |
| CN104621130A (zh) * | 2013-11-15 | 2015-05-20 | 南京华洲药业有限公司 | 一种含丙硫菌唑和嘧菌酯的杀菌组合物及其应用 |
| CN104186471B (zh) * | 2014-08-04 | 2017-11-28 | 广东中迅农科股份有限公司 | 一种含有氯氟氰虫酰胺和甲氧虫酰肼的农药组合物 |
| CN104322502A (zh) * | 2014-10-16 | 2015-02-04 | 浙江省化工研究院有限公司 | 一种含氯氟氰虫酰胺的农药组合物 |
| ES2879858T3 (es) | 2018-02-09 | 2021-11-23 | Rotam Agrochem Int Co Ltd | El uso de una mezcla fungicida para reducir la fitotoxicidad de cada fungicida individual |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1462043A (en) * | 1973-02-22 | 1977-01-19 | Ici Ltd | Process for combating fungi |
| US4367089A (en) * | 1980-10-08 | 1983-01-04 | E. I. Du Pont De Nemours And Company | Fungicidal carbamates of triazole ethanols (or ethenols) |
| CA2244526A1 (en) * | 1997-08-21 | 1999-02-21 | Bayer Corporation | Improved fungicide composition |
| US20010051175A1 (en) * | 1999-04-12 | 2001-12-13 | Strom Robert M. | Aqueous dispersions of agricultural chemicals |
| AR055627A1 (es) * | 2005-09-05 | 2007-08-29 | Cheminova As | Metodo de reduccion de la fitoxicidad en plantas suceptibles a fungicidas de triazol |
| EP2202228B1 (en) * | 2007-10-15 | 2014-12-10 | Takeda Pharmaceutical Company Limited | Amide compounds and use of the same |
| WO2010139410A2 (de) * | 2009-06-02 | 2010-12-09 | Bayer Cropscience Ag | Verwendung von succinat dehydrogenase inhibitoren zur kontrolle von sclerotinia ssp |
| EP2301350A1 (en) * | 2009-09-16 | 2011-03-30 | Bayer CropScience AG | Use of succinate dehydrogenase inhibitors for increasing the content of desired ingredients in crops |
-
2008
- 2008-06-10 BR BRPI0812799-9A2A patent/BRPI0812799A2/pt not_active IP Right Cessation
- 2008-06-10 US US12/665,283 patent/US20100184816A1/en not_active Abandoned
- 2008-06-10 WO PCT/EP2008/004610 patent/WO2009000407A1/de not_active Ceased
- 2008-06-16 CL CL2008001779A patent/CL2008001779A1/es unknown
- 2008-06-20 TW TW097122974A patent/TW200911117A/zh unknown
- 2008-06-26 AR ARP080102653A patent/AR067097A1/es not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| BRPI0812799A2 (pt) | 2014-09-30 |
| TW200911117A (en) | 2009-03-16 |
| CL2008001779A1 (es) | 2008-12-26 |
| US20100184816A1 (en) | 2010-07-22 |
| WO2009000407A1 (de) | 2008-12-31 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FA | Abandonment or withdrawal |