JP2012207012A5 - - Google Patents
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- Publication number
- JP2012207012A5 JP2012207012A5 JP2012037885A JP2012037885A JP2012207012A5 JP 2012207012 A5 JP2012207012 A5 JP 2012207012A5 JP 2012037885 A JP2012037885 A JP 2012037885A JP 2012037885 A JP2012037885 A JP 2012037885A JP 2012207012 A5 JP2012207012 A5 JP 2012207012A5
- Authority
- JP
- Japan
- Prior art keywords
- monomer unit
- solubility parameter
- solubility
- vinyl monomer
- term
- 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
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- 239000000178 monomer Substances 0.000 claims description 25
- 150000001875 compounds Chemical class 0.000 claims description 14
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 12
- 238000010557 suspension polymerization reaction Methods 0.000 claims description 4
- 239000002245 particle Substances 0.000 claims description 3
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims 5
- 229920002554 vinyl polymer Polymers 0.000 claims 5
- 229920000642 polymer Polymers 0.000 claims 4
- 230000003115 biocidal effect Effects 0.000 claims 2
- 239000003242 anti bacterial agent Substances 0.000 claims 1
- 238000013270 controlled release Methods 0.000 claims 1
- 239000002994 raw material Substances 0.000 claims 1
- 229910052739 hydrogen Inorganic materials 0.000 description 11
- 239000001257 hydrogen Substances 0.000 description 11
- 230000008018 melting Effects 0.000 description 9
- 238000002844 melting Methods 0.000 description 9
- -1 cineline Natural products 0.000 description 5
- WYVVKGNFXHOCQV-UHFFFAOYSA-N 3-iodoprop-2-yn-1-yl butylcarbamate Chemical compound CCCCNC(=O)OCC#CI WYVVKGNFXHOCQV-UHFFFAOYSA-N 0.000 description 2
- DBCAQXHNJOFNGC-UHFFFAOYSA-N 4-bromo-1,1,1-trifluorobutane Chemical compound FC(F)(F)CCCBr DBCAQXHNJOFNGC-UHFFFAOYSA-N 0.000 description 2
- YIVJZNGAASQVEM-UHFFFAOYSA-N Lauroyl peroxide Chemical compound CCCCCCCCCCCC(=O)OOC(=O)CCCCCCCCCCC YIVJZNGAASQVEM-UHFFFAOYSA-N 0.000 description 2
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 2
- 229920000297 Rayon Polymers 0.000 description 2
- 229960001591 cyfluthrin Drugs 0.000 description 2
- QQODLKZGRKWIFG-QSFXBCCZSA-N cyfluthrin Chemical compound CC1(C)[C@@H](C=C(Cl)Cl)[C@H]1C(=O)O[C@@H](C#N)C1=CC=C(F)C(OC=2C=CC=CC=2)=C1 QQODLKZGRKWIFG-QSFXBCCZSA-N 0.000 description 2
- STVZJERGLQHEKB-UHFFFAOYSA-N ethylene glycol dimethacrylate Substances CC(=C)C(=O)OCCOC(=O)C(C)=C STVZJERGLQHEKB-UHFFFAOYSA-N 0.000 description 2
- NYPJDWWKZLNGGM-UHFFFAOYSA-N fenvalerate Chemical compound C=1C=C(Cl)C=CC=1C(C(C)C)C(=O)OC(C#N)C(C=1)=CC=CC=1OC1=CC=CC=C1 NYPJDWWKZLNGGM-UHFFFAOYSA-N 0.000 description 2
- 239000000203 mixture Substances 0.000 description 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 description 2
- STJLVHWMYQXCPB-UHFFFAOYSA-N propiconazole Chemical compound O1C(CCC)COC1(C=1C(=CC(Cl)=CC=1)Cl)CN1N=CN=C1 STJLVHWMYQXCPB-UHFFFAOYSA-N 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- ZCVAOQKBXKSDMS-AQYZNVCMSA-N (+)-trans-allethrin Chemical compound CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)OC1C(C)=C(CC=C)C(=O)C1 ZCVAOQKBXKSDMS-AQYZNVCMSA-N 0.000 description 1
- 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
- FJDPATXIBIBRIM-QFMSAKRMSA-N (1R)-trans-cyphenothrin Chemical compound CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)OC(C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 FJDPATXIBIBRIM-QFMSAKRMSA-N 0.000 description 1
- FMTFEIJHMMQUJI-NJAFHUGGSA-N 102130-98-3 Natural products CC=CCC1=C(C)[C@H](CC1=O)OC(=O)[C@@H]1[C@@H](C=C(C)C)C1(C)C FMTFEIJHMMQUJI-NJAFHUGGSA-N 0.000 description 1
- RUMACXVDVNRZJZ-UHFFFAOYSA-N 2-methylpropyl 2-methylprop-2-enoate Chemical compound CC(C)COC(=O)C(C)=C RUMACXVDVNRZJZ-UHFFFAOYSA-N 0.000 description 1
- 229940044120 2-n-octyl-4-isothiazolin-3-one Drugs 0.000 description 1
- 229940099451 3-iodo-2-propynylbutylcarbamate Drugs 0.000 description 1
- 239000005652 Acrinathrin Substances 0.000 description 1
- 239000005877 Alpha-Cypermethrin Substances 0.000 description 1
- 239000005874 Bifenthrin Substances 0.000 description 1
- 239000005896 Etofenprox Substances 0.000 description 1
- 101000811217 Haloarcula marismortui (strain ATCC 43049 / DSM 3752 / JCM 8966 / VKM B-1809) 30S ribosomal protein S19e Proteins 0.000 description 1
- WOBHKFSMXKNTIM-UHFFFAOYSA-N Hydroxyethyl methacrylate Chemical compound CC(=C)C(=O)OCCO WOBHKFSMXKNTIM-UHFFFAOYSA-N 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 229930182984 Jasmolin Natural products 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- 239000005820 Prochloraz Substances 0.000 description 1
- 239000005822 Propiconazole Substances 0.000 description 1
- VQXSOUPNOZTNAI-UHFFFAOYSA-N Pyrethrin I Natural products CC(=CC1CC1C(=O)OC2CC(=O)C(=C2C)CC=C/C=C)C VQXSOUPNOZTNAI-UHFFFAOYSA-N 0.000 description 1
- IAXXETNIOYFMLW-GYSYKLTISA-N [(1r,3r,4r)-4,7,7-trimethyl-3-bicyclo[2.2.1]heptanyl] 2-methylprop-2-enoate Chemical compound C1C[C@@]2(C)[C@H](OC(=O)C(=C)C)C[C@@H]1C2(C)C IAXXETNIOYFMLW-GYSYKLTISA-N 0.000 description 1
- YLFSVIMMRPNPFK-WEQBUNFVSA-N acrinathrin Chemical compound CC1(C)[C@@H](\C=C/C(=O)OC(C(F)(F)F)C(F)(F)F)[C@H]1C(=O)O[C@H](C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 YLFSVIMMRPNPFK-WEQBUNFVSA-N 0.000 description 1
- 229940024113 allethrin Drugs 0.000 description 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 description 1
- HYFQSJHSFBMMMP-UHFFFAOYSA-N bis(4-fluorophenyl)methyl-(1,2,4-triazol-1-ylmethyl)silane Chemical compound C1=CC(F)=CC=C1C(C=1C=CC(F)=CC=1)[SiH2]CN1N=CN=C1 HYFQSJHSFBMMMP-UHFFFAOYSA-N 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- YREQHYQNNWYQCJ-UHFFFAOYSA-N etofenprox Chemical compound C1=CC(OCC)=CC=C1C(C)(C)COCC1=CC=CC(OC=2C=CC=CC=2)=C1 YREQHYQNNWYQCJ-UHFFFAOYSA-N 0.000 description 1
- 229950005085 etofenprox Drugs 0.000 description 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 description 1
- 238000009472 formulation Methods 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- JPMIIZHYYWMHDT-UHFFFAOYSA-N octhilinone Chemical compound CCCCCCCCN1SC=CC1=O JPMIIZHYYWMHDT-UHFFFAOYSA-N 0.000 description 1
- 150000003014 phosphoric acid esters Chemical class 0.000 description 1
- SMKRKQBMYOFFMU-UHFFFAOYSA-N prallethrin Chemical compound CC1(C)C(C=C(C)C)C1C(=O)OC1C(C)=C(CC#C)C(=O)C1 SMKRKQBMYOFFMU-UHFFFAOYSA-N 0.000 description 1
- HYJYGLGUBUDSLJ-UHFFFAOYSA-N pyrethrin Natural products CCC(=O)OC1CC(=C)C2CC3OC3(C)C2C2OC(=O)C(=C)C12 HYJYGLGUBUDSLJ-UHFFFAOYSA-N 0.000 description 1
- VJFUPGQZSXIULQ-XIGJTORUSA-N pyrethrin II Chemical compound CC1(C)[C@H](/C=C(\C)C(=O)OC)[C@H]1C(=O)O[C@@H]1C(C)=C(C\C=C/C=C)C(=O)C1 VJFUPGQZSXIULQ-XIGJTORUSA-N 0.000 description 1
- 239000002728 pyrethroid Substances 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000013268 sustained release Methods 0.000 description 1
- 239000012730 sustained-release form Substances 0.000 description 1
- YWSCPYYRJXKUDB-KAKFPZCNSA-N tralomethrin Chemical compound CC1(C)[C@@H](C(Br)C(Br)(Br)Br)[C@H]1C(=O)O[C@H](C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 YWSCPYYRJXKUDB-KAKFPZCNSA-N 0.000 description 1
- QORWJWZARLRLPR-UHFFFAOYSA-H tricalcium bis(phosphate) Chemical group [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O QORWJWZARLRLPR-UHFFFAOYSA-H 0.000 description 1
Priority Applications (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2012037885A JP6083936B2 (ja) | 2011-03-11 | 2012-02-23 | 徐放性粒子の製造方法 |
| PCT/JP2012/055968 WO2012124598A1 (ja) | 2011-03-11 | 2012-03-08 | 徐放性粒子 |
| CN2012800126121A CN103415207A (zh) | 2011-03-11 | 2012-03-08 | 缓释粒子 |
| US14/003,271 US9511030B2 (en) | 2011-03-11 | 2012-03-08 | Controlled release particles |
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2011054628 | 2011-03-11 | ||
| JP2011054628 | 2011-03-11 | ||
| JP2012037885A JP6083936B2 (ja) | 2011-03-11 | 2012-02-23 | 徐放性粒子の製造方法 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2012207012A JP2012207012A (ja) | 2012-10-25 |
| JP2012207012A5 true JP2012207012A5 (https=) | 2015-04-09 |
| JP6083936B2 JP6083936B2 (ja) | 2017-02-22 |
Family
ID=46830671
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2012037885A Active JP6083936B2 (ja) | 2011-03-11 | 2012-02-23 | 徐放性粒子の製造方法 |
Country Status (4)
| Country | Link |
|---|---|
| US (1) | US9511030B2 (https=) |
| JP (1) | JP6083936B2 (https=) |
| CN (1) | CN103415207A (https=) |
| WO (1) | WO2012124598A1 (https=) |
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP6109502B2 (ja) * | 2012-07-13 | 2017-04-05 | 大阪ガスケミカル株式会社 | 抗生物活性粒子およびその製造方法 |
| SG10201604814WA (en) | 2013-03-21 | 2016-08-30 | Eupraxia Pharmaceuticals USA LLC | Injectable sustained release composition and method of using the same for treating inflammation in joints and pain associated therewith |
| US10111424B2 (en) | 2013-05-17 | 2018-10-30 | 3M Innovative Properties Company | Release of biologically active agents from polymeric composite particles |
| WO2015030213A1 (ja) * | 2013-08-30 | 2015-03-05 | 日本エンバイロケミカルズ株式会社 | 徐放性粒子、その製造方法、成形材料および成形品 |
| CN105085778B (zh) * | 2014-04-22 | 2018-11-16 | 广东华润涂料有限公司 | 用于缓释功能成分的涂料组合物用水性胶乳、其制备方法以及应用 |
| EP3193847A4 (en) * | 2014-09-19 | 2018-06-06 | Eupraxia Pharmaceuticals Inc. | Injectable microparticles for hyper-localized release of therapeutic agents |
| MX2018005035A (es) | 2015-10-27 | 2018-09-06 | Eupraxia Pharmaceuticals Inc | Formulaciones de liberacion sostenida de anestesicos locales. |
| JP6830666B2 (ja) * | 2017-09-22 | 2021-02-17 | 新中村化学工業株式会社 | コアシェル型農薬粒剤組成物及びその製造方法 |
| US10881103B2 (en) * | 2017-11-06 | 2021-01-05 | National Chung Shan Institute Of Science And Technology | Biocide-encapsulated microcapsule for use in paint |
| US20230365761A1 (en) | 2020-09-11 | 2023-11-16 | Osaka Gas Chemicals Co., Ltd. | Additive for resin kneading |
| EP4304878A4 (en) * | 2021-03-08 | 2025-01-29 | Regents of the University of Michigan | Crosslinked ion-exchange materials, related methods, and related articles |
Family Cites Families (27)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS59145265A (ja) | 1983-02-04 | 1984-08-20 | Sumitomo Naugatuck Co Ltd | 接着剤組成物 |
| GB8331546D0 (en) | 1983-11-25 | 1984-01-04 | Exxon Research Engineering Co | Polymeric compositions |
| EP0143608B1 (en) | 1983-11-25 | 1992-07-22 | Ciba Specialty Chemicals Water Treatments Limited | Manufacture and use of polymeric beads |
| JPS6186941A (ja) | 1984-10-03 | 1986-05-02 | Japan Synthetic Rubber Co Ltd | 含油マイクロカプセルの製造方法 |
| JPH0699244B2 (ja) * | 1985-04-10 | 1994-12-07 | 日本ペイント株式会社 | 抗有害生物性を有する微小樹脂粒子 |
| US5225279A (en) * | 1985-04-30 | 1993-07-06 | Rohm And Haas Company | Solvent core encapsulant composition |
| DE4137619A1 (de) | 1991-11-15 | 1993-05-19 | Basf Ag | Mikrokapseln mit feststoff-kern |
| JPH0753835A (ja) * | 1993-08-10 | 1995-02-28 | Takeda Chem Ind Ltd | 有効成分を含有するコアポリマー、コアシェルポリマーおよびそれらの製造法 |
| DE19644224A1 (de) | 1996-10-24 | 1998-04-30 | Bayer Ag | Antifoulingbeschichtung |
| US5972363A (en) * | 1997-04-11 | 1999-10-26 | Rohm And Haas Company | Use of an encapsulated bioactive composition |
| DE19807118A1 (de) | 1998-02-20 | 1999-08-26 | Bayer Ag | Perlpolymerisat-Formulierungen |
| US7354596B1 (en) | 1998-05-01 | 2008-04-08 | 3M Innovative Properties Company | Anti-microbial agent delivery system |
| US6471975B1 (en) | 1998-05-01 | 2002-10-29 | 3M Innovative Properties Company | Microspheres as a delivery vehicle for bio-active agents useful in agricultural applications |
| DE60040411D1 (de) * | 1999-11-19 | 2008-11-13 | Nof Corp | Gerter freigabe und verfahren zu ihrer herstellung |
| JP4514077B2 (ja) | 1999-12-27 | 2010-07-28 | 日本エンバイロケミカルズ株式会社 | 微生物増殖抑制剤含有マイクロカプセルおよび微生物増殖抑制剤含有マイクロカプセルの製造方法 |
| JP2004331625A (ja) | 2003-05-12 | 2004-11-25 | Nof Corp | 水分散型のフェロモン徐放製剤およびその製造方法 |
| US20050282011A1 (en) | 2004-06-21 | 2005-12-22 | Nissin Chemical Industry Co., Ltd. | Microcapsule emulsion and method for producing the same |
| JP4842567B2 (ja) * | 2004-06-21 | 2011-12-21 | 日信化学工業株式会社 | マイクロカプセルエマルジョン及びその製造方法 |
| NO20071200L (no) | 2006-03-16 | 2007-09-17 | Rohm & Haas | Blandinger av innkapslede biocider |
| JP5045046B2 (ja) * | 2006-09-25 | 2012-10-10 | 住友化学株式会社 | 被覆粉状農薬 |
| JP4716435B2 (ja) | 2007-03-02 | 2011-07-06 | シチズン電子株式会社 | 光源装置及び光源装置を備えた表示装置 |
| JP2008239561A (ja) | 2007-03-28 | 2008-10-09 | Sumitomo Chemical Co Ltd | 常温で固体の生理活性物質のマイクロカプセル組成物の製造方法 |
| JP5125168B2 (ja) | 2007-03-28 | 2013-01-23 | 住友化学株式会社 | 常温で固体の生理活性物質のマイクロカプセル組成物の製造方法 |
| CN102480939B (zh) * | 2009-09-11 | 2014-11-05 | 日本环境化学株式会社 | 缓释性颗粒及其制造方法 |
| JP5763570B2 (ja) * | 2011-03-11 | 2015-08-12 | 大阪ガスケミカル株式会社 | 徐放性粒子およびその製造方法 |
| CN104023527A (zh) * | 2011-12-28 | 2014-09-03 | 日本环境化学株式会社 | 缓释性粒子、木材处理剂及其制造方法 |
| CN104411168A (zh) * | 2012-07-13 | 2015-03-11 | 日本环境化学株式会社 | 抗生物活性粒子及其制造方法 |
-
2012
- 2012-02-23 JP JP2012037885A patent/JP6083936B2/ja active Active
- 2012-03-08 US US14/003,271 patent/US9511030B2/en not_active Expired - Fee Related
- 2012-03-08 WO PCT/JP2012/055968 patent/WO2012124598A1/ja not_active Ceased
- 2012-03-08 CN CN2012800126121A patent/CN103415207A/zh active Pending
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