JP2006117940A5 - - Google Patents
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- Publication number
- JP2006117940A5 JP2006117940A5 JP2005305771A JP2005305771A JP2006117940A5 JP 2006117940 A5 JP2006117940 A5 JP 2006117940A5 JP 2005305771 A JP2005305771 A JP 2005305771A JP 2005305771 A JP2005305771 A JP 2005305771A JP 2006117940 A5 JP2006117940 A5 JP 2006117940A5
- Authority
- JP
- Japan
- Prior art keywords
- acrylate
- methacrylate
- alkyl
- crotonic acid
- propyl
- 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
- -1 pentyl - Chemical class 0.000 description 5
- 150000001875 compounds Chemical class 0.000 description 3
- 150000003141 primary amines Chemical class 0.000 description 3
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 description 2
- SOGAXMICEFXMKE-UHFFFAOYSA-N Butylmethacrylate Chemical compound CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 description 2
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 2
- WGQKYBSKWIADBV-UHFFFAOYSA-N benzylamine Chemical group NCC1=CC=CC=C1 WGQKYBSKWIADBV-UHFFFAOYSA-N 0.000 description 2
- 239000002981 blocking agent Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- GOXQRTZXKQZDDN-UHFFFAOYSA-N 2-Ethylhexyl acrylate Chemical compound CCCCC(CC)COC(=O)C=C GOXQRTZXKQZDDN-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- WDQMWEYDKDCEHT-UHFFFAOYSA-N 2-ethylhexyl 2-methylprop-2-enoate Chemical compound CCCCC(CC)COC(=O)C(C)=C WDQMWEYDKDCEHT-UHFFFAOYSA-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
- CFVWNXQPGQOHRJ-UHFFFAOYSA-N 2-methylpropyl prop-2-enoate Chemical compound CC(C)COC(=O)C=C CFVWNXQPGQOHRJ-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 1
- PAFZNILMFXTMIY-UHFFFAOYSA-N Cyclohexylamine Natural products NC1CCCCC1 PAFZNILMFXTMIY-UHFFFAOYSA-N 0.000 description 1
- HTJDQJBWANPRPF-UHFFFAOYSA-N Cyclopropylamine Chemical class NC1CC1 HTJDQJBWANPRPF-UHFFFAOYSA-N 0.000 description 1
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 1
- ZFDIRQKJPRINOQ-HWKANZROSA-N Ethyl crotonate Chemical compound CCOC(=O)\C=C\C ZFDIRQKJPRINOQ-HWKANZROSA-N 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
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 1
- 150000001299 aldehydes Chemical class 0.000 description 1
- 150000003973 alkyl amines Chemical class 0.000 description 1
- 125000005907 alkyl ester group Chemical group 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000011203 carbon fibre reinforced carbon Substances 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- LDHQCZJRKDOVOX-NSCUHMNNSA-N crotonic acid Chemical compound C\C=C\C(O)=O LDHQCZJRKDOVOX-NSCUHMNNSA-N 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- 150000003946 cyclohexylamines Chemical class 0.000 description 1
- SUPCQIBBMFXVTL-UHFFFAOYSA-N ethyl 2-methylprop-2-enoate Chemical compound CCOC(=O)C(C)=C SUPCQIBBMFXVTL-UHFFFAOYSA-N 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- JJWLVOIRVHMVIS-UHFFFAOYSA-N isopropylamine Chemical class CC(C)N JJWLVOIRVHMVIS-UHFFFAOYSA-N 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- MCVVUJPXSBQTRZ-ONEGZZNKSA-N methyl (e)-but-2-enoate Chemical compound COC(=O)\C=C\C MCVVUJPXSBQTRZ-ONEGZZNKSA-N 0.000 description 1
- FJDUDHYHRVPMJZ-UHFFFAOYSA-N nonan-1-amine Chemical compound CCCCCCCCCN FJDUDHYHRVPMJZ-UHFFFAOYSA-N 0.000 description 1
- 125000002347 octyl group Chemical class [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- BOQSSGDQNWEFSX-UHFFFAOYSA-N propan-2-yl 2-methylprop-2-enoate Chemical compound CC(C)OC(=O)C(C)=C BOQSSGDQNWEFSX-UHFFFAOYSA-N 0.000 description 1
- LYBIZMNPXTXVMV-UHFFFAOYSA-N propan-2-yl prop-2-enoate Chemical compound CC(C)OC(=O)C=C LYBIZMNPXTXVMV-UHFFFAOYSA-N 0.000 description 1
- ZHDCHCTZRODSEN-HWKANZROSA-N propyl (e)-but-2-enoate Chemical compound CCCOC(=O)\C=C\C ZHDCHCTZRODSEN-HWKANZROSA-N 0.000 description 1
- NHARPDSAXCBDDR-UHFFFAOYSA-N propyl 2-methylprop-2-enoate Chemical compound CCCOC(=O)C(C)=C NHARPDSAXCBDDR-UHFFFAOYSA-N 0.000 description 1
- PNXMTCDJUBJHQJ-UHFFFAOYSA-N propyl prop-2-enoate Chemical compound CCCOC(=O)C=C PNXMTCDJUBJHQJ-UHFFFAOYSA-N 0.000 description 1
- BHRZNVHARXXAHW-UHFFFAOYSA-N sec-butylamine Chemical compound CCC(C)N BHRZNVHARXXAHW-UHFFFAOYSA-N 0.000 description 1
- ISXSCDLOGDJUNJ-UHFFFAOYSA-N tert-butyl prop-2-enoate Chemical compound CC(C)(C)OC(=O)C=C ISXSCDLOGDJUNJ-UHFFFAOYSA-N 0.000 description 1
- YBRBMKDOPFTVDT-UHFFFAOYSA-N tert-butylamine Chemical compound CC(C)(C)N YBRBMKDOPFTVDT-UHFFFAOYSA-N 0.000 description 1
- LDHQCZJRKDOVOX-UHFFFAOYSA-N trans-crotonic acid Natural products CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 description 1
- ZFDIRQKJPRINOQ-UHFFFAOYSA-N transbutenic acid ethyl ester Natural products CCOC(=O)C=CC ZFDIRQKJPRINOQ-UHFFFAOYSA-N 0.000 description 1
- 150000007934 α,β-unsaturated carboxylic acids Chemical class 0.000 description 1
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US10/970,740 US7371807B2 (en) | 2004-10-21 | 2004-10-21 | Blocked biuretized isocyanates |
| US10/970740 | 2004-10-21 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2006117940A JP2006117940A (ja) | 2006-05-11 |
| JP2006117940A5 true JP2006117940A5 (enExample) | 2008-12-04 |
| JP4947952B2 JP4947952B2 (ja) | 2012-06-06 |
Family
ID=35428092
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2005305771A Expired - Fee Related JP4947952B2 (ja) | 2004-10-21 | 2005-10-20 | ブロックト・ビウレット化イソシアネート |
Country Status (13)
| Country | Link |
|---|---|
| US (1) | US7371807B2 (enExample) |
| EP (1) | EP1650245B1 (enExample) |
| JP (1) | JP4947952B2 (enExample) |
| KR (1) | KR20060054130A (enExample) |
| CN (1) | CN1769359A (enExample) |
| AT (1) | ATE381582T1 (enExample) |
| CA (1) | CA2523840C (enExample) |
| DE (1) | DE602005003898T2 (enExample) |
| ES (1) | ES2297585T3 (enExample) |
| MX (1) | MXPA05011280A (enExample) |
| NO (1) | NO20054853L (enExample) |
| RU (1) | RU2005132379A (enExample) |
| UA (1) | UA86369C2 (enExample) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7772307B2 (en) * | 2003-08-27 | 2010-08-10 | Great Eastern Resins Industrial Co., Ltd. | Water dispersible polyisocyanate composition and its uses |
| US20060089481A1 (en) * | 2004-10-21 | 2006-04-27 | Roesler Richard R | Blocked biuretized isocyanates |
| US7833692B2 (en) | 2007-03-12 | 2010-11-16 | Brewer Science Inc. | Amine-arresting additives for materials used in photolithographic processes |
| EP3950758A4 (en) * | 2019-03-29 | 2022-11-30 | Mitsui Chemicals, Inc. | CROSS-LINKING AGENT FOR FIBERS OR LEATHER |
Family Cites Families (28)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3976622A (en) | 1973-02-17 | 1976-08-24 | Bayer Aktiengesellschaft | Process for the production of polyisocyanates with a biuret structure |
| DE2308015B2 (de) | 1973-02-17 | 1980-07-31 | Bayer Ag, 5090 Leverkusen | Verfahren zur Herstellung von Polyisocyanaten mit Biuretstruktur |
| DE2507682A1 (de) * | 1975-02-22 | 1976-09-02 | Bayer Ag | Isocyanate |
| DE2730513A1 (de) | 1977-07-06 | 1979-01-25 | Bayer Ag | Verfahren zur herstellung von modifizierten polyisocyanaten |
| US4324979A (en) | 1979-06-21 | 1982-04-13 | National Research Development Corporation | Variable neutron collimator |
| US4495229A (en) | 1982-06-08 | 1985-01-22 | Chemische Werke Huls A.G. | One-component, heat-curing polyurethane-coatings, stable in storage |
| US4439593A (en) | 1983-05-26 | 1984-03-27 | Mobay Chemical Corporation | Polyurethane compositions with improved storage stability |
| US4518522A (en) | 1983-09-19 | 1985-05-21 | Mobay Chemical Corporation | Blocked polyisocyanates with improved storage stability |
| US5986033A (en) | 1984-02-29 | 1999-11-16 | The Baxenden Chemical Co. | Blocked isocyanates |
| DE3434881A1 (de) * | 1984-09-22 | 1986-04-03 | Hüls AG, 4370 Marl | Lagerstabile polyurethanharz-pulverlacke |
| US4677180A (en) | 1986-07-16 | 1987-06-30 | Mobay Corporation | Polyurethane compositions with improved storage stability |
| US4788262A (en) | 1986-12-08 | 1988-11-29 | Mobay Corporation | Polyisocyanate blends with improved compatibility with coreactants |
| US5071937A (en) | 1987-12-22 | 1991-12-10 | Mobay Corporation | Coating compositions based on blocked polyisocyanates and sterically hindered aromatic polyamines |
| US5370908A (en) | 1993-05-24 | 1994-12-06 | Olin Corporation | Low VOC, heat-curable, one-component and two-component coating compositions based on organic polyisocyanates |
| DE4324947A1 (de) | 1993-07-24 | 1995-01-26 | Basf Lacke & Farben | Nichtwäßrige Lacke |
| DE19505035A1 (de) | 1995-02-15 | 1996-08-22 | Basf Ag | Verfahren zur Herstellung biurethgruppen-haltigen Polyisocyanaten |
| DE19534624A1 (de) | 1995-09-18 | 1997-03-20 | Bayer Ag | Allophanatgruppen aufweisende Polyisocyanate auf Basis Diphenylmethandiisocyanat mit überwiegend oder vollständig blockierten Isocyanatgruppen |
| JP3712295B2 (ja) | 1996-04-12 | 2005-11-02 | 旭化成ケミカルズ株式会社 | ブロックポリイソシアネート組成物及びそれを用いた一液性熱硬化組成物 |
| DE19626886A1 (de) | 1996-07-04 | 1998-01-08 | Huels Chemische Werke Ag | Blockierte Polyisocyanate, ein Verfahren zu ihrer Herstellung sowie deren Verwendung |
| DE19748584A1 (de) | 1997-11-04 | 1999-05-06 | Basf Coatings Ag | Verfahren zur Herstellung einer mehrschichtigen Lackierung und für diese Verfahren geeignete Lacke |
| DE19813352A1 (de) | 1998-03-26 | 1999-09-30 | Bayer Ag | Malonesterblockierte Polyisocyanate mit Formaldehyd gegen Thermovergilbung |
| DE19941213A1 (de) | 1999-08-30 | 2001-03-01 | Bayer Ag | Malonester-blockiertes HDI-Trimerisat mit IPDA- und Formaldehydstabilisierung |
| MXPA04002650A (es) | 2001-09-21 | 2004-07-08 | Du Pont | Preparacion y uso de poliisocianatos que contienen biuret como agentes de reticulacion para recubrimientos. |
| DE10226931A1 (de) * | 2002-06-17 | 2003-12-24 | Bayer Ag | Polyurethan-Polyharnstoff Dispersionen |
| DE10226925A1 (de) * | 2002-06-17 | 2003-12-24 | Bayer Ag | Blockierte Polyisocyanate |
| US7026428B2 (en) | 2002-06-17 | 2006-04-11 | Bayer Aktiengesellschaft | Blocked polyisocyanates |
| DE10328993A1 (de) | 2003-06-27 | 2005-01-20 | Bayer Materialscience Ag | Blockierte Polyisocyanate |
| DE10328994A1 (de) * | 2003-06-27 | 2005-01-13 | Bayer Materialscience Ag | Blockierte Polyisocyanate |
-
2004
- 2004-10-21 US US10/970,740 patent/US7371807B2/en not_active Expired - Lifetime
-
2005
- 2005-10-08 EP EP05021975A patent/EP1650245B1/en not_active Expired - Lifetime
- 2005-10-08 ES ES05021975T patent/ES2297585T3/es not_active Expired - Lifetime
- 2005-10-08 DE DE602005003898T patent/DE602005003898T2/de not_active Expired - Lifetime
- 2005-10-08 AT AT05021975T patent/ATE381582T1/de not_active IP Right Cessation
- 2005-10-19 CA CA2523840A patent/CA2523840C/en not_active Expired - Fee Related
- 2005-10-20 MX MXPA05011280A patent/MXPA05011280A/es active IP Right Grant
- 2005-10-20 RU RU2005132379/04A patent/RU2005132379A/ru not_active Application Discontinuation
- 2005-10-20 UA UAA200509897A patent/UA86369C2/ru unknown
- 2005-10-20 NO NO20054853A patent/NO20054853L/no not_active Application Discontinuation
- 2005-10-20 KR KR1020050098973A patent/KR20060054130A/ko not_active Ceased
- 2005-10-20 JP JP2005305771A patent/JP4947952B2/ja not_active Expired - Fee Related
- 2005-10-21 CN CNA2005101162112A patent/CN1769359A/zh active Pending
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