JPWO2019084895A5 - - Google Patents
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- Publication number
- JPWO2019084895A5 JPWO2019084895A5 JP2020522868A JP2020522868A JPWO2019084895A5 JP WO2019084895 A5 JPWO2019084895 A5 JP WO2019084895A5 JP 2020522868 A JP2020522868 A JP 2020522868A JP 2020522868 A JP2020522868 A JP 2020522868A JP WO2019084895 A5 JPWO2019084895 A5 JP WO2019084895A5
- Authority
- JP
- Japan
- Prior art keywords
- solvent
- pesticide
- formulation
- weight percent
- ethyl
- 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.)
- Granted
Links
- 239000002904 solvent Substances 0.000 description 67
- 239000000575 pesticide Substances 0.000 description 42
- -1 ether ester Chemical class 0.000 description 17
- 239000003090 pesticide formulation Substances 0.000 description 15
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 13
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 13
- 229910052739 hydrogen Inorganic materials 0.000 description 12
- 239000001257 hydrogen Substances 0.000 description 12
- 125000004435 hydrogen atoms Chemical class [H]* 0.000 description 12
- 239000000203 mixture Substances 0.000 description 10
- 230000000052 comparative effect Effects 0.000 description 9
- 150000002170 ethers Chemical class 0.000 description 8
- 239000004480 active ingredient Substances 0.000 description 7
- 125000003118 aryl group Chemical group 0.000 description 7
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 7
- CTQNGGLPUBDAKN-UHFFFAOYSA-N o-xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 7
- 239000008096 xylene Substances 0.000 description 7
- 125000000217 alkyl group Chemical group 0.000 description 6
- 125000004432 carbon atoms Chemical group C* 0.000 description 6
- 238000000034 method Methods 0.000 description 6
- 239000005874 Bifenthrin Substances 0.000 description 5
- 238000004090 dissolution Methods 0.000 description 5
- 239000000463 material Substances 0.000 description 5
- 238000002360 preparation method Methods 0.000 description 5
- OMFRMAHOUUJSGP-IRHGGOMRSA-N κ-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 description 5
- 239000005885 Buprofezin Substances 0.000 description 4
- PRLVTUNWOQKEAI-UHFFFAOYSA-N buprofezin Chemical compound O=C1N(C(C)C)C(=NC(C)(C)C)SCN1C1=CC=CC=C1 PRLVTUNWOQKEAI-UHFFFAOYSA-N 0.000 description 4
- 239000000825 pharmaceutical preparation Substances 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- 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 3
- 239000005839 Tebuconazole Substances 0.000 description 3
- PXMNMQRDXWABCY-UHFFFAOYSA-N Tebuconazole Chemical compound C1=NC=NN1CC(O)(C(C)(C)C)CCC1=CC=C(Cl)C=C1 PXMNMQRDXWABCY-UHFFFAOYSA-N 0.000 description 3
- BHXIWUJLHYHGSJ-UHFFFAOYSA-N ethyl 3-ethoxypropanoate Chemical group CCOCCC(=O)OCC BHXIWUJLHYHGSJ-UHFFFAOYSA-N 0.000 description 3
- 238000009472 formulation Methods 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- FFSJPOPLSWBGQY-UHFFFAOYSA-N triazol-4-one Chemical compound O=C1C=NN=N1 FFSJPOPLSWBGQY-UHFFFAOYSA-N 0.000 description 3
- 239000003905 agrochemical Substances 0.000 description 2
- 239000003849 aromatic solvent Substances 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 230000001747 exhibiting Effects 0.000 description 2
- 229920001600 hydrophobic polymer Polymers 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 125000001424 substituent group Chemical group 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive Effects 0.000 description 1
- 239000002671 adjuvant Substances 0.000 description 1
- 230000000240 adjuvant Effects 0.000 description 1
- 230000000111 anti-oxidant Effects 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 230000001804 emulsifying Effects 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 231100000086 high toxicity Toxicity 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| PCT/CN2017/109246 WO2019084895A1 (en) | 2017-11-03 | 2017-11-03 | Solvents for agricultural applications and pesticide formulations |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2021510367A JP2021510367A (ja) | 2021-04-22 |
| JPWO2019084895A5 true JPWO2019084895A5 (zh) | 2022-11-09 |
| JP7227239B2 JP7227239B2 (ja) | 2023-02-21 |
Family
ID=66332778
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2020522868A Active JP7227239B2 (ja) | 2017-11-03 | 2017-11-03 | 農業用途のための溶媒および農薬製剤 |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US20200253196A1 (zh) |
| EP (1) | EP3704088A4 (zh) |
| JP (1) | JP7227239B2 (zh) |
| CN (1) | CN111247122B (zh) |
| BR (1) | BR112020008102B1 (zh) |
| CA (1) | CA3079265A1 (zh) |
| WO (1) | WO2019084895A1 (zh) |
Family Cites Families (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2504151A (en) * | 1948-02-12 | 1950-04-18 | Us Agriculture | Process of preparing methyl betafurfuryloxypropionate |
| JP3619261B2 (ja) * | 1993-06-15 | 2005-02-09 | 三菱レイヨン株式会社 | 溶剤組成物 |
| JPH11116994A (ja) * | 1997-10-17 | 1999-04-27 | Kyowa Yuka Kk | アルコキシ酪酸エステルからなる溶剤 |
| GB0129267D0 (en) * | 2001-12-06 | 2002-01-23 | Syngenta Ltd | Fungicides |
| DE10160008A1 (de) * | 2001-12-06 | 2003-06-18 | Haarmann & Reimer Gmbh | Verfahren zur Herstellung von Cyclohexyloxyessigsäurealkylestern |
| US7579017B2 (en) * | 2003-06-18 | 2009-08-25 | Brook Chandler Murphy | Physical mode of action pesticide |
| TWI386714B (zh) * | 2004-05-06 | 2013-02-21 | Dongjin Semichem Co Ltd | Ｔｆｔ-ｌｃｄ用層間有機絕緣膜、ｔｆｔ-ｌｃｄ用層間有機絕緣膜用丙烯酸系共聚合體樹脂及其製造方法 |
| EP2062875A1 (en) * | 2007-11-13 | 2009-05-27 | LABORATORIO FARMACEUTICO C.T. S.r.l. | New polymorphic forms of n-[4-(trifluoromethyl)benzyl]-4-methoxybutyramide |
| JP5365002B2 (ja) * | 2008-01-09 | 2013-12-11 | オート化学工業株式会社 | 硬化性組成物 |
| CN102007450B (zh) * | 2008-09-26 | 2015-01-21 | 株式会社Lg化学 | 用于黑矩阵的光敏树脂组合物 |
| EP3178320A1 (de) * | 2015-12-11 | 2017-06-14 | Bayer CropScience AG | Flüssige fungizid-haltige formulierungen |
| JP6792822B2 (ja) * | 2016-03-30 | 2020-12-02 | 学校法人神奈川大学 | 乳化組成物、製品、有機溶媒の含有量を低減させる方法、及び乳化剤の選択方法 |
-
2017
- 2017-11-03 WO PCT/CN2017/109246 patent/WO2019084895A1/en unknown
- 2017-11-03 CN CN201780096176.3A patent/CN111247122B/zh active Active
- 2017-11-03 CA CA3079265A patent/CA3079265A1/en active Pending
- 2017-11-03 US US16/638,416 patent/US20200253196A1/en not_active Abandoned
- 2017-11-03 JP JP2020522868A patent/JP7227239B2/ja active Active
- 2017-11-03 BR BR112020008102-7A patent/BR112020008102B1/pt active IP Right Grant
- 2017-11-03 EP EP17930200.5A patent/EP3704088A4/en active Pending
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