JP2013507388A - ポリアミン化合物を製造する方法 - Google Patents
ポリアミン化合物を製造する方法 Download PDFInfo
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- JP2013507388A JP2013507388A JP2012533352A JP2012533352A JP2013507388A JP 2013507388 A JP2013507388 A JP 2013507388A JP 2012533352 A JP2012533352 A JP 2012533352A JP 2012533352 A JP2012533352 A JP 2012533352A JP 2013507388 A JP2013507388 A JP 2013507388A
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- Prior art keywords
- methyl
- compound
- ethyl
- formula
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- Prior art date
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- 150000001875 compounds Chemical class 0.000 title claims abstract description 26
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 6
- 229920000768 polyamine Polymers 0.000 title description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims abstract description 22
- 238000000034 method Methods 0.000 claims abstract description 19
- 239000008199 coating composition Substances 0.000 claims abstract description 15
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims abstract description 13
- 125000000392 cycloalkenyl group Chemical group 0.000 claims abstract description 6
- SXRSQZLOMIGNAQ-UHFFFAOYSA-N Glutaraldehyde Chemical compound O=CCCCC=O SXRSQZLOMIGNAQ-UHFFFAOYSA-N 0.000 claims abstract description 5
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 7
- 239000004816 latex Substances 0.000 claims description 6
- 229920000126 latex Polymers 0.000 claims description 6
- 239000003638 chemical reducing agent Substances 0.000 claims description 5
- 125000005270 trialkylamine group Chemical group 0.000 claims description 5
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 4
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical group CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims description 3
- 125000001931 aliphatic group Chemical group 0.000 claims description 3
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims description 3
- 150000001412 amines Chemical class 0.000 abstract description 5
- 238000010979 pH adjustment Methods 0.000 abstract description 5
- 239000000126 substance Substances 0.000 abstract 1
- 239000000203 mixture Substances 0.000 description 14
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 12
- 239000012855 volatile organic compound Substances 0.000 description 10
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 9
- 239000000047 product Substances 0.000 description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- CBTVGIZVANVGBH-UHFFFAOYSA-N aminomethyl propanol Chemical compound CC(C)(N)CO CBTVGIZVANVGBH-UHFFFAOYSA-N 0.000 description 6
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 5
- 125000000217 alkyl group Chemical group 0.000 description 5
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 5
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 4
- 238000000576 coating method Methods 0.000 description 4
- 238000009472 formulation Methods 0.000 description 4
- HRPFQQALNDMRKK-UHFFFAOYSA-N 2,8-dimethyl-2,8-dinitrononane-3,7-diol Chemical compound [O-][N+](=O)C(C)(C)C(O)CCCC(O)C(C)(C)[N+]([O-])=O HRPFQQALNDMRKK-UHFFFAOYSA-N 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- 239000003054 catalyst Substances 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 229910052763 palladium Inorganic materials 0.000 description 3
- 229910052697 platinum Inorganic materials 0.000 description 3
- 239000000523 sample Substances 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 238000010998 test method Methods 0.000 description 3
- NQFWPSDMPHNIBC-UHFFFAOYSA-N 2,8-diamino-2,8-dimethylnonane-3,7-diol Chemical compound CC(C)(N)C(O)CCCC(O)C(C)(C)N NQFWPSDMPHNIBC-UHFFFAOYSA-N 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 2
- FGLBSLMDCBOPQK-UHFFFAOYSA-N 2-nitropropane Chemical compound CC(C)[N+]([O-])=O FGLBSLMDCBOPQK-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- SVYKKECYCPFKGB-UHFFFAOYSA-N N,N-dimethylcyclohexylamine Chemical compound CN(C)C1CCCCC1 SVYKKECYCPFKGB-UHFFFAOYSA-N 0.000 description 2
- UEEJHVSXFDXPFK-UHFFFAOYSA-N N-dimethylaminoethanol Chemical compound CN(C)CCO UEEJHVSXFDXPFK-UHFFFAOYSA-N 0.000 description 2
- 239000007868 Raney catalyst Substances 0.000 description 2
- 229910000564 Raney nickel Inorganic materials 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- 125000003342 alkenyl group Chemical group 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 229940125904 compound 1 Drugs 0.000 description 2
- 229940126214 compound 3 Drugs 0.000 description 2
- 125000004122 cyclic group Chemical group 0.000 description 2
- 229960002887 deanol Drugs 0.000 description 2
- 239000012972 dimethylethanolamine Substances 0.000 description 2
- 239000002270 dispersing agent Substances 0.000 description 2
- 230000014759 maintenance of location Effects 0.000 description 2
- 150000002828 nitro derivatives Chemical class 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
- 239000002243 precursor Substances 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- 239000006254 rheological additive Substances 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 238000000967 suction filtration Methods 0.000 description 2
- 0 *C(*)(C(CCCC(C(*)(*)N)O)O)N Chemical compound *C(*)(C(CCCC(C(*)(*)N)O)O)N 0.000 description 1
- XRIBIDPMFSLGFS-UHFFFAOYSA-N 2-(dimethylamino)-2-methylpropan-1-ol Chemical compound CN(C)C(C)(C)CO XRIBIDPMFSLGFS-UHFFFAOYSA-N 0.000 description 1
- SUGZATOHBPXTDV-UHFFFAOYSA-N 2-nitrobutane Chemical compound CCC(C)[N+]([O-])=O SUGZATOHBPXTDV-UHFFFAOYSA-N 0.000 description 1
- GSSXLFACIJSBOM-UHFFFAOYSA-N 2h-pyran-2-ol Chemical compound OC1OC=CC=C1 GSSXLFACIJSBOM-UHFFFAOYSA-N 0.000 description 1
- PNGUSDWLIDZUHD-UHFFFAOYSA-N 6-(2-aminopropan-2-yl)oxan-2-ol Chemical compound CC(C)(N)C1CCCC(O)O1 PNGUSDWLIDZUHD-UHFFFAOYSA-N 0.000 description 1
- ZZKLJZUITAYAAN-UHFFFAOYSA-N 6-(2-nitropropan-2-yl)oxan-2-ol Chemical compound [O-][N+](=O)C(C)(C)C1CCCC(O)O1 ZZKLJZUITAYAAN-UHFFFAOYSA-N 0.000 description 1
- WDWSFTMSGDMZDK-UHFFFAOYSA-N 6-methyl-6-nitroheptane-1,5-diol Chemical compound [O-][N+](=O)C(C)(C)C(O)CCCCO WDWSFTMSGDMZDK-UHFFFAOYSA-N 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 238000006842 Henry reaction Methods 0.000 description 1
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 1
- JGFZNNIVVJXRND-UHFFFAOYSA-N N,N-Diisopropylethylamine (DIPEA) Chemical compound CCN(C(C)C)C(C)C JGFZNNIVVJXRND-UHFFFAOYSA-N 0.000 description 1
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
- 229920013802 TRITON CF-10 Polymers 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000008065 acid anhydrides Chemical class 0.000 description 1
- 239000013543 active substance Substances 0.000 description 1
- AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical class [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 239000008346 aqueous phase Substances 0.000 description 1
- -1 bis-AMP compounds Chemical class 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 125000002843 carboxylic acid group Chemical group 0.000 description 1
- 150000001793 charged compounds Chemical class 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 125000000753 cycloalkyl group Chemical group 0.000 description 1
- 239000013530 defoamer Substances 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 239000012634 fragment Substances 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 238000002290 gas chromatography-mass spectrometry Methods 0.000 description 1
- 238000004128 high performance liquid chromatography Methods 0.000 description 1
- 125000001183 hydrocarbyl group Chemical group 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 238000005984 hydrogenation reaction Methods 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 239000005457 ice water Substances 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- VMOWKUTXPNPTEN-UHFFFAOYSA-N n,n-dimethylpropan-2-amine Chemical compound CC(C)N(C)C VMOWKUTXPNPTEN-UHFFFAOYSA-N 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- 230000003472 neutralizing effect Effects 0.000 description 1
- NJNQUTDUIPVROZ-UHFFFAOYSA-N nitrocyclohexane Chemical compound [O-][N+](=O)C1CCCCC1 NJNQUTDUIPVROZ-UHFFFAOYSA-N 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- 239000012074 organic phase Substances 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 239000012071 phase Substances 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- 238000010926 purge Methods 0.000 description 1
- 239000008213 purified water Substances 0.000 description 1
- 238000007655 standard test method Methods 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- 238000004448 titration Methods 0.000 description 1
- GPRLSGONYQIRFK-MNYXATJNSA-N triton Chemical compound [3H+] GPRLSGONYQIRFK-MNYXATJNSA-N 0.000 description 1
- 239000011882 ultra-fine particle Substances 0.000 description 1
- 238000001291 vacuum drying Methods 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C201/00—Preparation of esters of nitric or nitrous acid or of compounds containing nitro or nitroso groups bound to a carbon skeleton
- C07C201/06—Preparation of nitro compounds
- C07C201/12—Preparation of nitro compounds by reactions not involving the formation of nitro groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C213/00—Preparation of compounds containing amino and hydroxy, amino and etherified hydroxy or amino and esterified hydroxy groups bound to the same carbon skeleton
- C07C213/02—Preparation of compounds containing amino and hydroxy, amino and etherified hydroxy or amino and esterified hydroxy groups bound to the same carbon skeleton by reactions involving the formation of amino groups from compounds containing hydroxy groups or etherified or esterified hydroxy groups
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/16—Nitrogen-containing compounds
- C08K5/17—Amines; Quaternary ammonium compounds
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Paints Or Removers (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Abstract
Description
他に示されない限りは、全てのパーセンテージは重量パーセンテージ(重量%)である。百万分率での濃度(ppm)は重量/体積基準で計算される。「水性」組成物は水を少なくとも30重量%、あるいは水を少なくとも35重量%、あるいは水を少なくとも38重量%含む組成物である。好ましくは、水性組成物は5重量%を超えて有機溶媒を含まない。他に特定されない限りは、「アルキル」基は線状もしくは分岐の配置の1〜20個の炭素原子を有するヒドロカルビル基である。アルケニル基は1以上の二重結合、好ましくは1つの二重結合を有するアルキル基である。「シクロアルキル」もしくは「シクロアルケニル」基は少なくとも1つの環を含むアルキルもしくはアルケニル基である。
コーティングのための原料のVOC(揮発性有機化合物)含量は、不揮発性材料(NVM)含量および水含量を測定し、次いでその残部をVOCとして計算することにより決定される。これら測定は、米国においてコーティング配合物のVOC含量を決定するために使用される方法であるUSEPA試験方法24によって特定される手順に従って行われる。
1.POLYPHOBE(ポリフォーブ)TR−116:高効率レオロジー調節剤
2.POLYPHOBE(ポリフォーブ)TR−117:レオロジー調節剤
3.TAMOL(タモール)1124:分散剤
4.STRODEX(ストロデックス)PK−95G:エマルションのための分散/湿潤剤として使用される酸無水物界面活性剤
5.TRITON(トライトン)CF−10:非イオン性界面活性剤
6.RHODOLINE(ロドライン)643:オールベースの脱泡剤
7.TIPURE(タイピュア)R−706:二酸化チタン顔料
8.POLYGLOSS(ポリグロス)90:水系および溶媒系コーティングの双方において、容易な分散および向上した光沢を提供するように設計された超微粒子サイズで高光沢のカオリン
9.UCARラテックス300:ビニルアクリルポリマー
Claims (10)
- R1がメチルであり、R2がメチルもしくはエチルであるか、またはR1とR2とが一緒になってシクロヘキシル基を形成している、請求項1に記載の方法。
- R1がメチルであり、かつR2がメチルもしくはエチルである請求項2に記載の方法。
- R1がメチルであり、かつR2がメチルもしくはエチルである請求項4に記載の方法。
- R1がメチルであり、R2がメチルもしくはエチルであるか、またはR1とR2とが一緒になってシクロヘキシル基を形成している、請求項6に記載の方法。
- 水性コーティング組成物が、アクリル酸、メタクリル酸またはこれらの組み合わせの重合単位を含むアクリルラテックスである請求項7に記載の方法。
- R1がメチルであり、かつR2がメチルもしくはエチルである請求項8に記載の方法。
- アクリルラテックスの当初pHが2〜7である請求項9に記載の方法。
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US27853009P | 2009-10-08 | 2009-10-08 | |
US61/278,530 | 2009-10-08 | ||
PCT/US2010/052004 WO2011044478A1 (en) | 2009-10-08 | 2010-10-08 | Method for preparing polyamine compounds |
Publications (2)
Publication Number | Publication Date |
---|---|
JP2013507388A true JP2013507388A (ja) | 2013-03-04 |
JP5562426B2 JP5562426B2 (ja) | 2014-07-30 |
Family
ID=43500456
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2012533352A Active JP5562426B2 (ja) | 2009-10-08 | 2010-10-08 | ポリアミン化合物を製造する方法 |
Country Status (7)
Country | Link |
---|---|
US (1) | US8692031B2 (ja) |
EP (1) | EP2464621B1 (ja) |
JP (1) | JP5562426B2 (ja) |
CN (1) | CN102712567B (ja) |
BR (1) | BR112012007986B8 (ja) |
CA (1) | CA2775388C (ja) |
WO (1) | WO2011044478A1 (ja) |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE10318143A1 (de) | 2003-03-08 | 2004-09-23 | Brillux Gmbh & Co. Kg | Beschichtungsmittel mit Farbumschlag |
DE502004004117D1 (de) * | 2003-03-08 | 2007-08-02 | Brillux Gmbh & Co Kg | Beschichtungsmittel mit Farbumschlag |
CN100363421C (zh) * | 2005-02-05 | 2008-01-23 | 广州慧谷化学有限公司 | 一种热固性丙烯酸乳液及其制备方法以及含有该乳液的涂料 |
-
2010
- 2010-10-08 CA CA2775388A patent/CA2775388C/en active Active
- 2010-10-08 JP JP2012533352A patent/JP5562426B2/ja active Active
- 2010-10-08 WO PCT/US2010/052004 patent/WO2011044478A1/en active Application Filing
- 2010-10-08 US US13/500,449 patent/US8692031B2/en active Active
- 2010-10-08 BR BR112012007986A patent/BR112012007986B8/pt active IP Right Grant
- 2010-10-08 CN CN201080044986.2A patent/CN102712567B/zh active Active
- 2010-10-08 EP EP10765729.8A patent/EP2464621B1/en active Active
Non-Patent Citations (3)
Title |
---|
JPN6013039900; Olester Benson et al.: The Journal of Organic Chemistry 53, 1988, p.3036-3045 * |
JPN6013039902; 第5版 実験化学講座14 有機化合物の合成II-アルコール・アミン- 第5版,第2刷, 20070415, 第448-450頁, 丸善株式会社 * |
JPN6013039903; 第4版 実験化学講座20 有機合成II-アルコール・アミン- 第4版,第3刷, 19960425, 第380-381頁, 丸善株式会社 * |
Also Published As
Publication number | Publication date |
---|---|
CA2775388A1 (en) | 2011-04-14 |
CN102712567B (zh) | 2014-06-25 |
CN102712567A (zh) | 2012-10-03 |
EP2464621B1 (en) | 2013-06-05 |
WO2011044478A1 (en) | 2011-04-14 |
BR112012007986B1 (pt) | 2021-11-16 |
BR112012007986B8 (pt) | 2021-12-21 |
CA2775388C (en) | 2014-09-09 |
BR112012007986A2 (pt) | 2016-03-29 |
EP2464621A1 (en) | 2012-06-20 |
US8692031B2 (en) | 2014-04-08 |
US20120202934A1 (en) | 2012-08-09 |
JP5562426B2 (ja) | 2014-07-30 |
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