JP2013526492A5 - - Google Patents
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- JP2013526492A5 JP2013526492A5 JP2013509457A JP2013509457A JP2013526492A5 JP 2013526492 A5 JP2013526492 A5 JP 2013526492A5 JP 2013509457 A JP2013509457 A JP 2013509457A JP 2013509457 A JP2013509457 A JP 2013509457A JP 2013526492 A5 JP2013526492 A5 JP 2013526492A5
- Authority
- JP
- Japan
- Prior art keywords
- esters
- branched
- linear
- component
- composition according
- Prior art date
- Legal status (The legal status 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 status listed.)
- Pending
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- 239000000203 mixture Substances 0.000 claims 20
- 150000002148 esters Chemical class 0.000 claims 14
- 239000000194 fatty acid Substances 0.000 claims 8
- 239000003139 biocide Substances 0.000 claims 7
- 230000003115 biocidal effect Effects 0.000 claims 6
- 125000004432 carbon atom Chemical group C* 0.000 claims 6
- -1 triketone Chemical compound 0.000 claims 6
- 235000014113 dietary fatty acids Nutrition 0.000 claims 5
- 229930195729 fatty acid Natural products 0.000 claims 5
- 239000003921 oil Substances 0.000 claims 5
- 235000019198 oils Nutrition 0.000 claims 5
- 150000001298 alcohols Chemical class 0.000 claims 4
- 239000006184 cosolvent Substances 0.000 claims 3
- 239000003995 emulsifying agent Substances 0.000 claims 3
- 150000004665 fatty acids Chemical class 0.000 claims 3
- 150000002191 fatty alcohols Chemical class 0.000 claims 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 2
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 claims 2
- KAESVJOAVNADME-UHFFFAOYSA-N Pyrrole Chemical compound C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 claims 2
- 239000002671 adjuvant Substances 0.000 claims 2
- 235000010233 benzoic acid Nutrition 0.000 claims 2
- 150000001559 benzoic acids Chemical class 0.000 claims 2
- USIUVYZYUHIAEV-UHFFFAOYSA-N diphenyl ether Chemical compound C=1C=CC=CC=1OC1=CC=CC=C1 USIUVYZYUHIAEV-UHFFFAOYSA-N 0.000 claims 2
- 229910052739 hydrogen Inorganic materials 0.000 claims 2
- 239000001257 hydrogen Substances 0.000 claims 2
- 150000004702 methyl esters Chemical class 0.000 claims 2
- 229920005862 polyol Polymers 0.000 claims 2
- 150000003077 polyols Chemical class 0.000 claims 2
- 229920006395 saturated elastomer Polymers 0.000 claims 2
- 235000015112 vegetable and seed oil Nutrition 0.000 claims 2
- 239000008158 vegetable oil Substances 0.000 claims 2
- ZXQYGBMAQZUVMI-RDDWSQKMSA-N (1S)-cis-(alphaR)-cyhalothrin Chemical compound CC1(C)[C@H](\C=C(/Cl)C(F)(F)F)[C@@H]1C(=O)O[C@@H](C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 ZXQYGBMAQZUVMI-RDDWSQKMSA-N 0.000 claims 1
- ZMYFCFLJBGAQRS-IRXDYDNUSA-N (2R,3S)-epoxiconazole Chemical compound C1=CC(F)=CC=C1[C@@]1(CN2N=CN=C2)[C@H](C=2C(=CC=CC=2)Cl)O1 ZMYFCFLJBGAQRS-IRXDYDNUSA-N 0.000 claims 1
- HOKKPVIRMVDYPB-UVTDQMKNSA-N (Z)-thiacloprid Chemical compound C1=NC(Cl)=CC=C1CN1C(=N/C#N)/SCC1 HOKKPVIRMVDYPB-UVTDQMKNSA-N 0.000 claims 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 claims 1
- IEGRLEZDTRNPRH-UHFFFAOYSA-N 2-hydroxyiminocyclohexan-1-one Chemical compound ON=C1CCCCC1=O IEGRLEZDTRNPRH-UHFFFAOYSA-N 0.000 claims 1
- QMEQBOSUJUOXMX-UHFFFAOYSA-N 2h-oxadiazine Chemical compound N1OC=CC=N1 QMEQBOSUJUOXMX-UHFFFAOYSA-N 0.000 claims 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 claims 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 claims 1
- OEDUIFSDODUDRK-UHFFFAOYSA-N 5-phenyl-1h-pyrazole Chemical compound N1N=CC=C1C1=CC=CC=C1 OEDUIFSDODUDRK-UHFFFAOYSA-N 0.000 claims 1
- HOSGXJWQVBHGLT-UHFFFAOYSA-N 6-hydroxy-3,4-dihydro-1h-quinolin-2-one Chemical group N1C(=O)CCC2=CC(O)=CC=C21 HOSGXJWQVBHGLT-UHFFFAOYSA-N 0.000 claims 1
- VTNQPKFIQCLBDU-UHFFFAOYSA-N Acetochlor Chemical compound CCOCN(C(=O)CCl)C1=C(C)C=CC=C1CC VTNQPKFIQCLBDU-UHFFFAOYSA-N 0.000 claims 1
- 239000005730 Azoxystrobin Substances 0.000 claims 1
- 239000005874 Bifenthrin Substances 0.000 claims 1
- 239000005944 Chlorpyrifos Substances 0.000 claims 1
- 239000005892 Deltamethrin Substances 0.000 claims 1
- 239000005767 Epoxiconazole Substances 0.000 claims 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims 1
- 239000005775 Fenbuconazole Substances 0.000 claims 1
- 239000005899 Fipronil Substances 0.000 claims 1
- 239000005558 Fluroxypyr Substances 0.000 claims 1
- 239000005562 Glyphosate Substances 0.000 claims 1
- 239000005906 Imidacloprid Substances 0.000 claims 1
- 239000005907 Indoxacarb Substances 0.000 claims 1
- HRYILSDLIGTCOP-UHFFFAOYSA-N N-benzoylurea Chemical compound NC(=O)NC(=O)C1=CC=CC=C1 HRYILSDLIGTCOP-UHFFFAOYSA-N 0.000 claims 1
- 239000005590 Oxyfluorfen Substances 0.000 claims 1
- OQMBBFQZGJFLBU-UHFFFAOYSA-N Oxyfluorfen Chemical compound C1=C([N+]([O-])=O)C(OCC)=CC(OC=2C(=CC(=CC=2)C(F)(F)F)Cl)=C1 OQMBBFQZGJFLBU-UHFFFAOYSA-N 0.000 claims 1
- 229910019142 PO4 Inorganic materials 0.000 claims 1
- 239000005822 Propiconazole Substances 0.000 claims 1
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 claims 1
- 229930182692 Strobilurin Natural products 0.000 claims 1
- 239000005839 Tebuconazole Substances 0.000 claims 1
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 claims 1
- 239000005940 Thiacloprid Substances 0.000 claims 1
- 239000002253 acid Substances 0.000 claims 1
- 150000007513 acids Chemical class 0.000 claims 1
- 125000002252 acyl group Chemical group 0.000 claims 1
- 239000001361 adipic acid Substances 0.000 claims 1
- 235000011037 adipic acid Nutrition 0.000 claims 1
- 125000001931 aliphatic group Chemical group 0.000 claims 1
- 125000005907 alkyl ester group Chemical group 0.000 claims 1
- 125000000217 alkyl group Chemical group 0.000 claims 1
- 125000002947 alkylene group Chemical group 0.000 claims 1
- 150000003931 anilides Chemical class 0.000 claims 1
- 239000003945 anionic surfactant Substances 0.000 claims 1
- 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 claims 1
- OMFRMAHOUUJSGP-IRHGGOMRSA-N bifenthrin Chemical compound C1=CC=C(C=2C=CC=CC=2)C(C)=C1COC(=O)[C@@H]1[C@H](\C=C(/Cl)C(F)(F)F)C1(C)C OMFRMAHOUUJSGP-IRHGGOMRSA-N 0.000 claims 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 claims 1
- VXIVSQZSERGHQP-UHFFFAOYSA-N chloroacetamide Chemical compound NC(=O)CCl VXIVSQZSERGHQP-UHFFFAOYSA-N 0.000 claims 1
- SBPBAQFWLVIOKP-UHFFFAOYSA-N chlorpyrifos Chemical compound CCOP(=S)(OCC)OC1=NC(Cl)=C(Cl)C=C1Cl SBPBAQFWLVIOKP-UHFFFAOYSA-N 0.000 claims 1
- 150000001934 cyclohexanes Chemical class 0.000 claims 1
- 229960002483 decamethrin Drugs 0.000 claims 1
- OWZREIFADZCYQD-NSHGMRRFSA-N deltamethrin Chemical compound CC1(C)[C@@H](C=C(Br)Br)[C@H]1C(=O)O[C@H](C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 OWZREIFADZCYQD-NSHGMRRFSA-N 0.000 claims 1
- 150000001983 dialkylethers Chemical class 0.000 claims 1
- 229940013764 fipronil Drugs 0.000 claims 1
- MEFQWPUMEMWTJP-UHFFFAOYSA-N fluroxypyr Chemical compound NC1=C(Cl)C(F)=NC(OCC(O)=O)=C1Cl MEFQWPUMEMWTJP-UHFFFAOYSA-N 0.000 claims 1
- 238000009472 formulation Methods 0.000 claims 1
- 239000000417 fungicide Substances 0.000 claims 1
- XDDAORKBJWWYJS-UHFFFAOYSA-N glyphosate Chemical compound OC(=O)CNCP(O)(O)=O XDDAORKBJWWYJS-UHFFFAOYSA-N 0.000 claims 1
- 229940097068 glyphosate Drugs 0.000 claims 1
- 239000004009 herbicide Substances 0.000 claims 1
- WNLRTRBMVRJNCN-UHFFFAOYSA-N hexanedioic acid Natural products OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 claims 1
- 229930195733 hydrocarbon Natural products 0.000 claims 1
- 150000002430 hydrocarbons Chemical class 0.000 claims 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 1
- YWTYJOPNNQFBPC-UHFFFAOYSA-N imidacloprid Chemical compound [O-][N+](=O)\N=C1/NCCN1CC1=CC=C(Cl)N=C1 YWTYJOPNNQFBPC-UHFFFAOYSA-N 0.000 claims 1
- 229940056881 imidacloprid Drugs 0.000 claims 1
- VBCVPMMZEGZULK-NRFANRHFSA-N indoxacarb Chemical compound C([C@@]1(OC2)C(=O)OC)C3=CC(Cl)=CC=C3C1=NN2C(=O)N(C(=O)OC)C1=CC=C(OC(F)(F)F)C=C1 VBCVPMMZEGZULK-NRFANRHFSA-N 0.000 claims 1
- 239000002917 insecticide Substances 0.000 claims 1
- 150000003903 lactic acid esters Chemical class 0.000 claims 1
- 239000005910 lambda-Cyhalothrin Substances 0.000 claims 1
- 239000007788 liquid Substances 0.000 claims 1
- 239000002480 mineral oil Substances 0.000 claims 1
- 239000002736 nonionic surfactant Substances 0.000 claims 1
- IDOWTHOLJBTAFI-UHFFFAOYSA-N phenmedipham Chemical compound COC(=O)NC1=CC=CC(OC(=O)NC=2C=C(C)C=CC=2)=C1 IDOWTHOLJBTAFI-UHFFFAOYSA-N 0.000 claims 1
- BSCCSDNZEIHXOK-UHFFFAOYSA-N phenyl carbamate Chemical compound NC(=O)OC1=CC=CC=C1 BSCCSDNZEIHXOK-UHFFFAOYSA-N 0.000 claims 1
- 239000010452 phosphate Substances 0.000 claims 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 claims 1
- SIOXPEMLGUPBBT-UHFFFAOYSA-N picolinic acid Chemical compound OC(=O)C1=CC=CC=N1 SIOXPEMLGUPBBT-UHFFFAOYSA-N 0.000 claims 1
- 239000005648 plant growth regulator Substances 0.000 claims 1
- 150000003138 primary alcohols Chemical class 0.000 claims 1
- LFULEKSKNZEWOE-UHFFFAOYSA-N propanil Chemical compound CCC(=O)NC1=CC=C(Cl)C(Cl)=C1 LFULEKSKNZEWOE-UHFFFAOYSA-N 0.000 claims 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 claims 1
- 239000002728 pyrethroid Substances 0.000 claims 1
- 238000007142 ring opening reaction Methods 0.000 claims 1
- 150000003839 salts Chemical class 0.000 claims 1
- 229920002545 silicone oil Polymers 0.000 claims 1
- 150000003626 triacylglycerols Chemical class 0.000 claims 1
- UFTFJSFQGQCHQW-UHFFFAOYSA-N triformin Chemical compound O=COCC(OC=O)COC=O UFTFJSFQGQCHQW-UHFFFAOYSA-N 0.000 claims 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP10004859.4A EP2384624B1 (en) | 2010-05-08 | 2010-05-08 | Biocide compositions comprising alkoxylated oligoglycerol esters |
| EPEP10004859 | 2010-05-08 | ||
| PCT/EP2011/001579 WO2011141093A1 (en) | 2010-05-08 | 2011-03-30 | Biocide compositions comprising alkoxylated oligoglycerol esters |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2013526492A JP2013526492A (ja) | 2013-06-24 |
| JP2013526492A5 true JP2013526492A5 (enExample) | 2014-05-15 |
Family
ID=43412015
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2013509457A Pending JP2013526492A (ja) | 2010-05-08 | 2011-03-30 | アルコキシ化オリゴグリセロールエステルを含むバイオサイド組成物 |
Country Status (13)
| Country | Link |
|---|---|
| US (1) | US8980867B2 (enExample) |
| EP (1) | EP2384624B1 (enExample) |
| JP (1) | JP2013526492A (enExample) |
| KR (1) | KR20130100901A (enExample) |
| CN (1) | CN102970866B (enExample) |
| AU (1) | AU2011252440B2 (enExample) |
| BR (1) | BR112012028559B1 (enExample) |
| CA (1) | CA2798654C (enExample) |
| ES (1) | ES2541592T3 (enExample) |
| IL (1) | IL222853B (enExample) |
| RU (1) | RU2560590C2 (enExample) |
| UA (1) | UA109135C2 (enExample) |
| WO (1) | WO2011141093A1 (enExample) |
Families Citing this family (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US9591854B2 (en) | 2012-06-18 | 2017-03-14 | Basf Se | Agroformulations containing a lactone based alkoxylate |
| US20140206541A1 (en) * | 2013-01-24 | 2014-07-24 | Cognis Ip Management Gmbh | Agricultural Compositions Comprising Mono Or Dicarboxylic Acid Esters Of Polyhydric Alcohols |
| RU2632959C2 (ru) | 2013-08-14 | 2017-10-11 | Крода, Инк. | Уменьшение сноса при опрыскивании |
| CN105451551B (zh) * | 2013-08-14 | 2018-09-07 | 禾大公司 | 助剂组合 |
| US10370493B2 (en) * | 2016-01-29 | 2019-08-06 | Evonik Degussa Gmbh | Polyglycerol alkoxylate esters and preparation and use thereof |
| EP3490378B1 (en) * | 2016-07-29 | 2021-10-13 | Basf Se | A method for controlling insects where an alkoxylated glycerol is applied to soil |
| AU2019300109B2 (en) * | 2018-07-10 | 2025-04-10 | Bayer Aktiengesellschaft | Novel carrier fluids for liquid fungal spore formulations |
| CN113613497B (zh) | 2019-04-03 | 2023-10-03 | 克里尔利夫公司 | 胶态银基组合物及其用于预防和控制植物病害的方法 |
| AU2019236750B2 (en) * | 2019-09-27 | 2023-02-23 | Imtrade Australia Pty Ltd | Chlorpyrifos formulation |
| WO2025037126A1 (en) * | 2023-08-12 | 2025-02-20 | Sartipi Sasan | The compounds to combat fungal and bacterial with plant disease |
Family Cites Families (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DD268147A1 (de) | 1988-01-13 | 1989-05-24 | Akad Wissenschaften Ddr | Herbizides mittel |
| CA2081652C (en) * | 1991-10-31 | 2002-09-10 | Yuichi Hioki | Agricultural chemical composition |
| JP3228571B2 (ja) * | 1991-10-31 | 2001-11-12 | 花王株式会社 | 農薬用効力増強剤及び農薬組成物 |
| FR2729307B1 (fr) | 1995-01-18 | 1997-04-18 | Seppic Sa | Utilisation d'esters d'acides gras ethoxyles comme composants auto-emulsionnables notamment utiles pour la preparation de produits de traitement phytosanitaires ou de medicaments a usage veterinaire ou humain |
| GB9703054D0 (en) * | 1997-02-14 | 1997-04-02 | Ici Plc | Agrochemical surfactant compositions |
| WO2001008481A1 (de) * | 1999-07-30 | 2001-02-08 | Clariant Gmbh | Pestizidzubereitungen enthaltend polyglycerine oder polyglycerinderivate |
| CR6243A (es) * | 1999-09-20 | 2008-04-16 | Syngenta Participations Ag | Formulaciones plaguicidas que contienen tensoactivo de poliarilfenolfosfatoester alcoxilado y tensoactivo de lignosulfonato alcoxilado |
| DE10000320A1 (de) * | 2000-01-07 | 2001-07-12 | Cognis Deutschland Gmbh | Wäßriges herbizides Mittel |
| DE10132459A1 (de) | 2001-07-04 | 2003-01-23 | Cognis Deutschland Gmbh | Verfahren zur Verbesserung der Regenfestigkeit von Pflanzenschutzmitteln |
| DE10211801B4 (de) * | 2002-03-16 | 2004-09-30 | Clariant Gmbh | Kosmetische und pharmazeutische Zubereitungen enthaltend einen oxalkylierten Polyglycerinester |
| DE10233701A1 (de) * | 2002-07-24 | 2004-02-05 | Basf Ag | Entschäumer und/oder Entlüfter für wässrige, zur Schaumbildung neigende Medien |
| DE10307171B4 (de) | 2003-02-20 | 2009-04-16 | Clariant Produkte (Deutschland) Gmbh | Copolymere enthaltende landwirschaftliche Mittel |
| DE10340540A1 (de) * | 2003-09-01 | 2005-03-24 | Basf Ag | Emulgatorfreie Entschäumer, Verfahren zu ihrer Herstellung und ihre Verwendung |
| JP2007045708A (ja) * | 2005-08-05 | 2007-02-22 | Asahi Breweries Ltd | 植物害虫防除剤組成物 |
| JP4931388B2 (ja) * | 2005-09-07 | 2012-05-16 | アサヒグループホールディングス株式会社 | 植物病害抵抗性遺伝子活性化用組成物 |
| JP2008141967A (ja) * | 2006-12-06 | 2008-06-26 | Kao Corp | 麦類の増収方法 |
| JP2008162912A (ja) * | 2006-12-27 | 2008-07-17 | Kao Corp | 根粒の増加方法 |
-
2010
- 2010-05-08 EP EP10004859.4A patent/EP2384624B1/en not_active Not-in-force
- 2010-05-08 ES ES10004859.4T patent/ES2541592T3/es active Active
-
2011
- 2011-03-30 JP JP2013509457A patent/JP2013526492A/ja active Pending
- 2011-03-30 WO PCT/EP2011/001579 patent/WO2011141093A1/en not_active Ceased
- 2011-03-30 AU AU2011252440A patent/AU2011252440B2/en not_active Ceased
- 2011-03-30 CN CN201180033613.XA patent/CN102970866B/zh not_active Expired - Fee Related
- 2011-03-30 UA UAA201213922A patent/UA109135C2/uk unknown
- 2011-03-30 US US13/696,891 patent/US8980867B2/en active Active
- 2011-03-30 KR KR1020127030607A patent/KR20130100901A/ko not_active Withdrawn
- 2011-03-30 BR BR112012028559-9A patent/BR112012028559B1/pt not_active IP Right Cessation
- 2011-03-30 CA CA2798654A patent/CA2798654C/en not_active Expired - Fee Related
- 2011-03-30 RU RU2012147935/13A patent/RU2560590C2/ru not_active IP Right Cessation
-
2012
- 2012-11-05 IL IL222853A patent/IL222853B/en not_active IP Right Cessation
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