JP2008526922A - ポリウレア化合物 - Google Patents
ポリウレア化合物 Download PDFInfo
- Publication number
- JP2008526922A JP2008526922A JP2007550788A JP2007550788A JP2008526922A JP 2008526922 A JP2008526922 A JP 2008526922A JP 2007550788 A JP2007550788 A JP 2007550788A JP 2007550788 A JP2007550788 A JP 2007550788A JP 2008526922 A JP2008526922 A JP 2008526922A
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- JP
- Japan
- Prior art keywords
- monoamine
- polyurea compound
- polyurea
- chiral
- mixture
- 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.)
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- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/08—Processes
- C08G18/16—Catalysts
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C273/00—Preparation of urea or its derivatives, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups
- C07C273/18—Preparation of urea or its derivatives, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups of substituted ureas
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/2805—Compounds having only one group containing active hydrogen
- C08G18/285—Nitrogen containing compounds
- C08G18/2865—Compounds having only one primary or secondary amino group; Ammonia
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
- C08G18/72—Polyisocyanates or polyisothiocyanates
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D11/00—Inks
- C09D11/02—Printing inks
- C09D11/03—Printing inks characterised by features other than the chemical nature of the binder
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D5/00—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
- C09D5/04—Thixotropic paints
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D7/00—Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
- C09D7/40—Additives
- C09D7/43—Thickening agents
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L75/00—Compositions of polyureas or polyurethanes; Compositions of derivatives of such polymers
- C08L75/02—Polyureas
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- Chemical Kinetics & Catalysis (AREA)
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- Wood Science & Technology (AREA)
- Health & Medical Sciences (AREA)
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- Polymers & Plastics (AREA)
- General Chemical & Material Sciences (AREA)
- Polyurethanes Or Polyureas (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Paints Or Removers (AREA)
- Inks, Pencil-Leads, Or Crayons (AREA)
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| US65445505P | 2005-02-22 | 2005-02-22 | |
| PCT/EP2006/050134 WO2006075000A1 (en) | 2005-01-11 | 2006-01-10 | A polyurea compound |
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| JP2008526922A true JP2008526922A (ja) | 2008-07-24 |
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| EP (1) | EP1846469B1 (https=) |
| JP (2) | JP2008526922A (https=) |
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| CN (2) | CN101103061B (https=) |
| BR (1) | BRPI0606710A2 (https=) |
| RU (1) | RU2007130730A (https=) |
| WO (1) | WO2006075000A1 (https=) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2015155486A (ja) * | 2014-02-19 | 2015-08-27 | 東ソー株式会社 | ポリオール組成物 |
| KR101835720B1 (ko) * | 2015-11-30 | 2018-03-08 | 케이에스케미칼 주식회사 | 전단유동화 특성을 갖는 점탄성 조절제의 제조방법 |
| JP2018059096A (ja) * | 2016-09-30 | 2018-04-12 | ライオン株式会社 | 液体洗浄剤組成物 |
| WO2019235256A1 (ja) * | 2018-06-05 | 2019-12-12 | 東京エレクトロン株式会社 | 成膜用組成物および成膜装置 |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2006074895A1 (en) * | 2005-01-11 | 2006-07-20 | Nuplex Resins B.V. | Commixtures for use in rheology modification |
| FR2907336A1 (fr) * | 2006-10-19 | 2008-04-25 | Oreal | Vernis a ongles contenant un agent gelifiant polyuree |
| GB2462105A (en) * | 2008-07-24 | 2010-01-27 | Nuplex Resins Bv | Thixotropic aqueous coating composition |
| US20130203934A1 (en) * | 2010-04-09 | 2013-08-08 | Bayer Materialscience Llc | Two-component, polyaspartic coating compositions |
| CN102372655B (zh) * | 2010-08-26 | 2014-03-26 | 中国石油化工股份有限公司 | 一种碳酰四胺化合物及其制备方法 |
| EP2463340A1 (de) | 2010-12-09 | 2012-06-13 | Sika Technology AG | Thixotrope Polyharnstoffaddukte |
| CN105985724A (zh) | 2011-10-07 | 2016-10-05 | 树脂核动力工业有限公司 | 可交联组合物 |
| EP2644632A1 (en) * | 2012-03-29 | 2013-10-02 | Huntsman International Llc | Isocyanate-based prepolymer |
| EP2644633A1 (en) * | 2012-03-29 | 2013-10-02 | Huntsman International Llc | Isocyanate-based prepolymer |
| ES2669524T3 (es) | 2013-04-08 | 2018-05-28 | Allnex Netherlands B.V. | Composición reticulable por reacción de adición de Michael Real (RMA) |
| US20150175836A1 (en) * | 2013-12-19 | 2015-06-25 | Axalta Coating Systems Ip Co., Llc | Low bake temperature curable coating compositions and processes for producing coatings at low bake temperatures |
| US20150175834A1 (en) * | 2013-12-19 | 2015-06-25 | Axalta Coating Systems Ip Co., Llc | Low bake temperature curable coating compositions and processes for producing coatings at low bake temperatures |
| US9856384B2 (en) * | 2014-07-21 | 2018-01-02 | Axalta Coatings Systems Ip Co., Llc | Sag control compositions, methods of forming the same, and methods of forming coating systems using the same |
| PL3283587T3 (pl) | 2015-04-17 | 2024-07-22 | Allnex Netherlands B.V. | Sieciowalne rma kompozycje i sieciowalne rma żywice do powłok łatwych do czyszczenia |
| EP3283585B1 (en) | 2015-04-17 | 2023-11-15 | Allnex Netherlands B.V. | Adhesion promotor for real michael addition crosslinkable compositions |
| JP6837991B2 (ja) | 2015-04-17 | 2021-03-03 | オールネックス・ネザーランズ・ビー．ブイ．Ａｌｌｎｅｘ Ｎｅｔｈｅｒｌａｎｄｓ Ｂ．Ｖ． | フロアコーティング組成物 |
| EP3283583A1 (en) | 2015-04-17 | 2018-02-21 | Allnex Netherlands B.V. | Process for the manufacture of a crosslinkable composition |
| US10407385B2 (en) * | 2015-07-27 | 2019-09-10 | Byk-Chemie Gmbh | Ureaurethanes for rheology control |
| WO2018012552A1 (ja) * | 2016-07-15 | 2018-01-18 | 関西ペイント株式会社 | 塗料組成物 |
| CN109923144B (zh) * | 2016-11-07 | 2022-03-22 | 湛新荷兰有限公司 | 制备触变性组合物的方法 |
| JP7187483B2 (ja) * | 2017-12-28 | 2022-12-12 | 関西ペイント株式会社 | 塗料組成物 |
| EP3663326A1 (en) | 2018-12-04 | 2020-06-10 | Allnex Netherlands B.V. | Rma crosslinkable polymer |
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| CN111349370A (zh) * | 2020-04-24 | 2020-06-30 | 湖南湘江关西涂料有限公司 | 高触变性树脂及其制备方法与应用、涂料 |
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| MX2023012346A (es) * | 2021-04-28 | 2023-10-27 | Allnex Netherlands Bv | Proceso para la aplicacion sin exceso de pulverizacion de una composicion de resina y composiciones de resina para usarse en el proceso. |
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Family Cites Families (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3367920A (en) * | 1964-11-24 | 1968-02-06 | Merck & Co Inc | Polyurea and method of preparing same |
| US3620695A (en) * | 1969-04-10 | 1971-11-16 | Texaco Inc | Thickened compositions and process of preparing them |
| US4165329A (en) * | 1972-06-02 | 1979-08-21 | Chevron Research Company | Grease thickening agent |
| NL176864C (nl) | 1976-11-25 | 1985-06-17 | Akzo Nv | Werkwijze voor de bereiding van een thixotrope bekledingssamenstelling. |
| US4528319A (en) * | 1984-07-20 | 1985-07-09 | General Motors Corporation | Sag control of high solid polyurethane clearcoats by urea thixotrope/silica systems |
| JPH0637602B2 (ja) | 1986-09-25 | 1994-05-18 | 日本油脂株式会社 | 塗料用流動性制御剤 |
| US5176907A (en) * | 1991-08-13 | 1993-01-05 | The Johns Hopkins University School Of Medicine | Biocompatible and biodegradable poly (phosphoester-urethanes) |
| ZA981569B (en) * | 1997-04-08 | 1999-08-25 | Du Pont | An engineered seed protein having a higher percentage of essential amino acids. |
| US7196154B2 (en) * | 2000-12-11 | 2007-03-27 | Light Black Inc. | Method of producing polymer resins |
| DE60237243D1 (de) * | 2001-10-26 | 2010-09-16 | Nuplex Resins Bv | Nadelförmige kristalle von diharnstoffderivaten die sich von hydrazin ableiten und ihre verwendung zur veränderung der rheology in überzugszusammensetzungen und klebstoffen |
| US20050119422A1 (en) * | 2002-04-24 | 2005-06-02 | Basf Corporation | Thermally curable, thixotropic mixtures containing carbamate and/or allophanate groups |
| AU2003258013A1 (en) * | 2002-08-01 | 2004-02-23 | California Institute Of Technology | Synthesis of macrocyclic polymers by ring insertion polymerization of cyclic olefin monomers |
| EP1641888B1 (en) | 2003-07-08 | 2012-02-29 | Nuplex Resins B.V. | Amino acid derivatives and their use as a sag control agent |
| KR101317545B1 (ko) * | 2005-06-28 | 2013-10-15 | 누플렉스 레진스 비브이 | 요변성 레올로지 개량제로서의 폴리우레아 생성물 |
-
2006
- 2006-01-10 US US11/795,095 patent/US8742052B2/en active Active
- 2006-01-10 WO PCT/EP2006/050134 patent/WO2006075000A1/en not_active Ceased
- 2006-01-10 JP JP2007550788A patent/JP2008526922A/ja not_active Withdrawn
- 2006-01-10 EP EP06700743.5A patent/EP1846469B1/en not_active Expired - Lifetime
- 2006-01-10 RU RU2007130730/04A patent/RU2007130730A/ru not_active Application Discontinuation
- 2006-01-10 KR KR1020077016675A patent/KR20070100947A/ko not_active Withdrawn
- 2006-01-10 CN CN2006800020901A patent/CN101103061B/zh not_active Expired - Lifetime
- 2006-01-10 BR BRPI0606710A patent/BRPI0606710A2/pt not_active IP Right Cessation
- 2006-01-10 JP JP2007550741A patent/JP2008527126A/ja not_active Withdrawn
- 2006-01-10 CN CNA2006800020865A patent/CN101103060A/zh active Pending
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2015155486A (ja) * | 2014-02-19 | 2015-08-27 | 東ソー株式会社 | ポリオール組成物 |
| KR101835720B1 (ko) * | 2015-11-30 | 2018-03-08 | 케이에스케미칼 주식회사 | 전단유동화 특성을 갖는 점탄성 조절제의 제조방법 |
| JP2018059096A (ja) * | 2016-09-30 | 2018-04-12 | ライオン株式会社 | 液体洗浄剤組成物 |
| JP7004537B2 (ja) | 2016-09-30 | 2022-01-21 | ライオン株式会社 | 粒子分散洗浄剤組成物 |
| WO2019235256A1 (ja) * | 2018-06-05 | 2019-12-12 | 東京エレクトロン株式会社 | 成膜用組成物および成膜装置 |
Also Published As
| Publication number | Publication date |
|---|---|
| EP1846469A1 (en) | 2007-10-24 |
| CN101103061B (zh) | 2011-03-02 |
| WO2006075000A1 (en) | 2006-07-20 |
| CN101103061A (zh) | 2008-01-09 |
| JP2008527126A (ja) | 2008-07-24 |
| US20080139755A1 (en) | 2008-06-12 |
| EP1846469B1 (en) | 2014-04-30 |
| RU2007130730A (ru) | 2009-02-20 |
| US8742052B2 (en) | 2014-06-03 |
| BRPI0606710A2 (pt) | 2017-07-11 |
| CN101103060A (zh) | 2008-01-09 |
| KR20070100947A (ko) | 2007-10-15 |
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