JP5551673B2 - 低vocポリアミン - Google Patents
低vocポリアミン Download PDFInfo
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- JP5551673B2 JP5551673B2 JP2011254494A JP2011254494A JP5551673B2 JP 5551673 B2 JP5551673 B2 JP 5551673B2 JP 2011254494 A JP2011254494 A JP 2011254494A JP 2011254494 A JP2011254494 A JP 2011254494A JP 5551673 B2 JP5551673 B2 JP 5551673B2
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- compound
- heteroalkyl
- methyl
- alkyl
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- 229920000768 polyamine Polymers 0.000 title description 3
- 150000001875 compounds Chemical class 0.000 claims description 49
- 125000000217 alkyl group Chemical group 0.000 claims description 27
- 125000004404 heteroalkyl group Chemical group 0.000 claims description 24
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 20
- 125000003118 aryl group Chemical group 0.000 claims description 19
- 230000001588 bifunctional effect Effects 0.000 claims description 17
- 239000001257 hydrogen Substances 0.000 claims description 14
- 229910052739 hydrogen Inorganic materials 0.000 claims description 14
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 13
- 229910052757 nitrogen Inorganic materials 0.000 claims description 11
- 239000008199 coating composition Substances 0.000 claims description 10
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 9
- 150000002431 hydrogen Chemical class 0.000 claims description 9
- 229910052799 carbon Inorganic materials 0.000 claims description 7
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 7
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 5
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 5
- 238000000034 method Methods 0.000 claims description 4
- -1 heteroalkyl nitrogen atom Compound Chemical class 0.000 claims description 3
- 239000000203 mixture Substances 0.000 description 14
- YADISKICBOYXFS-UHFFFAOYSA-N 2-ethyl-2-nitropropane-1,3-diol Chemical compound CCC(CO)(CO)[N+]([O-])=O YADISKICBOYXFS-UHFFFAOYSA-N 0.000 description 10
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 10
- 238000006243 chemical reaction Methods 0.000 description 10
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 10
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 9
- 239000011541 reaction mixture Substances 0.000 description 8
- 239000000047 product Substances 0.000 description 7
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 6
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 5
- NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 description 5
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 5
- GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 4
- 238000004128 high performance liquid chromatography Methods 0.000 description 4
- 230000014759 maintenance of location Effects 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- MCSXGCZMEPXKIW-UHFFFAOYSA-N 3-hydroxy-4-[(4-methyl-2-nitrophenyl)diazenyl]-N-(3-nitrophenyl)naphthalene-2-carboxamide Chemical compound Cc1ccc(N=Nc2c(O)c(cc3ccccc23)C(=O)Nc2cccc(c2)[N+]([O-])=O)c(c1)[N+]([O-])=O MCSXGCZMEPXKIW-UHFFFAOYSA-N 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 3
- 125000002252 acyl group Chemical group 0.000 description 3
- 125000003545 alkoxy group Chemical group 0.000 description 3
- 125000004432 carbon atom Chemical group C* 0.000 description 3
- 239000003054 catalyst Substances 0.000 description 3
- 239000003638 chemical reducing agent Substances 0.000 description 3
- 125000005843 halogen group Chemical group 0.000 description 3
- 238000005984 hydrogenation reaction Methods 0.000 description 3
- 239000004816 latex Substances 0.000 description 3
- 229920000126 latex Polymers 0.000 description 3
- 229910052763 palladium Inorganic materials 0.000 description 3
- 229910052697 platinum Inorganic materials 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- 125000001424 substituent group Chemical group 0.000 description 3
- 238000006467 substitution reaction Methods 0.000 description 3
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 2
- GYKQZYIQBBLJLM-UHFFFAOYSA-N 2-ethyl-2-nitrobutan-1-ol Chemical compound CCC(CC)(CO)[N+]([O-])=O GYKQZYIQBBLJLM-UHFFFAOYSA-N 0.000 description 2
- LOTYADDQWWVBDJ-UHFFFAOYSA-N 2-methyl-2-nitropropane-1,3-diol Chemical compound OCC(C)(CO)[N+]([O-])=O LOTYADDQWWVBDJ-UHFFFAOYSA-N 0.000 description 2
- 0 CC(C)(*)CN1CCN(CC(C)(C)*)CC1 Chemical compound CC(C)(*)CN1CCN(CC(C)(C)*)CC1 0.000 description 2
- RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 2
- 239000007868 Raney catalyst Substances 0.000 description 2
- 229910000564 Raney nickel Inorganic materials 0.000 description 2
- NPXOKRUENSOPAO-UHFFFAOYSA-N Raney nickel Chemical compound [Al].[Ni] NPXOKRUENSOPAO-UHFFFAOYSA-N 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- 125000003277 amino group Chemical group 0.000 description 2
- 238000004458 analytical method Methods 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 150000001721 carbon Chemical group 0.000 description 2
- 239000007795 chemical reaction product Substances 0.000 description 2
- 125000001072 heteroaryl group Chemical group 0.000 description 2
- 239000011346 highly viscous material Substances 0.000 description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 2
- 238000004895 liquid chromatography mass spectrometry Methods 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- KVKFRMCSXWQSNT-UHFFFAOYSA-N n,n'-dimethylethane-1,2-diamine Chemical compound CNCCNC KVKFRMCSXWQSNT-UHFFFAOYSA-N 0.000 description 2
- 150000002828 nitro derivatives Chemical class 0.000 description 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 2
- 238000010979 pH adjustment Methods 0.000 description 2
- 229920006395 saturated elastomer Polymers 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 238000000967 suction filtration Methods 0.000 description 2
- 125000002030 1,2-phenylene group Chemical group [H]C1=C([H])C([*:1])=C([*:2])C([H])=C1[H] 0.000 description 1
- 125000001989 1,3-phenylene group Chemical group [H]C1=C([H])C([*:1])=C([H])C([*:2])=C1[H] 0.000 description 1
- 125000001140 1,4-phenylene group Chemical group [H]C1=C([H])C([*:2])=C([H])C([H])=C1[*:1] 0.000 description 1
- PCNWBUOSTLGPMI-UHFFFAOYSA-N 2-nitro-1-propanol Chemical compound OCC(C)[N+]([O-])=O PCNWBUOSTLGPMI-UHFFFAOYSA-N 0.000 description 1
- DHEAPCCWWIZJRQ-UHFFFAOYSA-N CCC(CN(C)CCN(C)CC(CC)(CO)[N+]([O-])=O)(CO)[N+]([O-])=O Chemical compound CCC(CN(C)CCN(C)CC(CC)(CO)[N+]([O-])=O)(CO)[N+]([O-])=O DHEAPCCWWIZJRQ-UHFFFAOYSA-N 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 1
- 229920000305 Nylon 6,10 Polymers 0.000 description 1
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 1
- JEDZLBFUGJTJGQ-UHFFFAOYSA-N [Na].COCCO[AlH]OCCOC Chemical compound [Na].COCCO[AlH]OCCOC JEDZLBFUGJTJGQ-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical class [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 description 1
- 125000004103 aminoalkyl group Chemical group 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 125000002843 carboxylic acid group Chemical group 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 125000004093 cyano group Chemical group *C#N 0.000 description 1
- 230000008034 disappearance Effects 0.000 description 1
- 239000008098 formaldehyde solution Substances 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 238000004817 gas chromatography Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 125000005842 heteroatom Chemical group 0.000 description 1
- 125000001183 hydrocarbyl group Chemical group 0.000 description 1
- 125000004356 hydroxy functional group Chemical group O* 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 239000012280 lithium aluminium hydride Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- MCSAJNNLRCFZED-UHFFFAOYSA-N nitroethane Chemical compound CC[N+]([O-])=O MCSAJNNLRCFZED-UHFFFAOYSA-N 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 125000004430 oxygen atom Chemical group O* 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 125000006413 ring segment Chemical group 0.000 description 1
- 239000012419 sodium bis(2-methoxyethoxy)aluminum hydride Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 238000001291 vacuum drying Methods 0.000 description 1
- 239000003039 volatile agent Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
- C07D295/04—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms
- C07D295/08—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly bound oxygen or sulfur atoms
- C07D295/084—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly bound oxygen or sulfur atoms with the ring nitrogen atoms and the oxygen or sulfur atoms attached to the same carbon chain, which is not interrupted by carbocyclic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C215/00—Compounds containing amino and hydroxy groups bound to the same carbon skeleton
- C07C215/02—Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton
- C07C215/04—Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being saturated
- C07C215/06—Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being saturated and acyclic
- C07C215/14—Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being saturated and acyclic the nitrogen atom of the amino group being further bound to hydrocarbon groups substituted by amino groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Paints Or Removers (AREA)
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。アルキル基は場合によっては1以上の二重結合もしくは三重結合を有する。アルキル基上での1以上のヒドロキシもしくはアルコキシ基の置換が許容される。好ましくは、アルキル基は飽和かつ非置換である。「シクロアルキル」基は少なくとも1つの飽和環を含むアルキル基である。「ヘテロアルキル」基は少なくとも1つの炭素がO、NRもしくはS(ここで、Rは水素、アルキル、アリール、アルアルキルもしくは−CH 2 C(Y)(R 1 )(CH 2 OH)基(ここでYは化合物(II)もしくは化合物(I)においてそれぞれNO 2 もしくはNH 2 である)である)によって置き換えられたアルキル基であり、例えば、−CH2CHR’(OCH2CHR’)n−(ここで、R’は水素、メチルもしくはエチルであり、nは1〜9、またはそのヘテロアルキル基の最大サイズおよびR’の種類(identity)によって決定される上限である)である。ヘテロアルキル基の炭素数はそのヘテロアルキル基における実際の炭素原子の数であって、組み込まれたヘテロ原子を含まない。本発明のある実施形態においては、ヘテロアルキル基は酸素へテロ原子だけを有し、かつ炭素原子:酸素原子の比率は5:1〜2:1、あるいは4:1〜2.5:1である。本発明のある実施形態においては、ヘテロアルキル基は窒素へテロ原子だけを有し、かつ炭素原子:窒素原子の比率は2以上:1である。本発明のある実施形態においては、少なくとも1つの窒素原子を含むヘテロアルキル基は窒素原子に結合した−CH2C(Y)(R1)(CH2OH)基を有し、ここでYは化合物(II)もしくは化合物(I)においてそれぞれNO2もしくはNH2である。本発明のある実施形態においては、ヘテロアルキル基はその鎖のいずれかの末端で炭素原子を介して結合されている。「アリール」基は芳香族炭化水素化合物から得られる置換基である。アリール基は、他に特定されない限りは、全部で6〜20個の環原子を有し、かつ別々もしくは縮合した1以上の環を有する。「アルアルキル」基は「アリール」基で置換された「アルキル」基である。「アリールアルキル」基はアルキル基に二官能性アリール基が挿入されている二官能性基であって、例えば、−(CH2)xC6H4(CH2)y−であり、ここでC6H4はo−、m−もしくはp−フェニレンであり、xおよびyは同じかもしくは異なっていてよく、好ましくは同じであり、かつアリールアルキル基の全体のサイズおよび挿入されたアリール基の種類と調和した値を有する。「アリールヘテロアルキル」基はヘテロアルキル基に二官能性アリール基が挿入されている二官能性基である。アリール基上での以下の基の1種以上の置換が許容される:ハロ、シアノ、ニトロ、ヒドロキシ、アルコキシ、アルキル、ヘテロアルキル、アルカノイル、アミノ、または1以上のアルキル、アリール、アルアルキル、ヘテロアルキルもしくはアルカノイルで置換されたアミノ;1以上のハロ基による置換がアルキル、ヘテロアルキル、アルカノイルもしくはアルコキシ基上で可能である。好ましくは、アリール基はハロゲン原子を含まない。本発明のある好ましい実施形態においては、アリール基は非置換であるか、またはアルキル基だけで置換されている。二官能性基は2つの結合点を有する置換基であり、例えば、二官能性アルキル基の例は、−(CH2)x−(ここで、xは2〜20であり得る)であろう。
1H NMR(DMSO−d6):δ1.46(s,6H)、δ2.50(s,2H)、δ3.17(s,8H)、δ3.7(s,4H)およびδ5.31(d,4H)。13C NMR(DMSO−d6):δ16.8、48.5、54.5、63.9および93.0ppm。
Claims (10)
- XがC 4 −C8ヘテロアルキルである請求項1に記載の化合物。
- R2がCH2C(NH2)(R1)(CH2OH)である請求項2に記載の化合物。
- Xが少なくとも1つの窒素原子を有するC4−C8ヘテロアルキル基であり、CH2C(NH2)(R1)(CH2OH)基がヘテロアルキル窒素原子に結合している請求項3に記載の化合物。
- XがC 4 −C8ヘテロアルキルである請求項5に記載の化合物。
- R2がCH2C(NO2)(R1)(CH2OH)である請求項6に記載の化合物。
- XがC 4 −C8ヘテロアルキルである請求項8に記載の方法。
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US201061427273P | 2010-12-27 | 2010-12-27 | |
US61/427,273 | 2010-12-27 |
Publications (2)
Publication Number | Publication Date |
---|---|
JP2012136508A JP2012136508A (ja) | 2012-07-19 |
JP5551673B2 true JP5551673B2 (ja) | 2014-07-16 |
Family
ID=45093443
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2011254494A Active JP5551673B2 (ja) | 2010-12-27 | 2011-11-22 | 低vocポリアミン |
Country Status (6)
Country | Link |
---|---|
US (1) | US8288464B2 (ja) |
EP (1) | EP2468713B1 (ja) |
JP (1) | JP5551673B2 (ja) |
CN (1) | CN102584607B (ja) |
BR (1) | BRPI1107063B1 (ja) |
CA (1) | CA2759341C (ja) |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CA2759346C (en) * | 2010-12-27 | 2014-01-28 | Dow Global Technologies Llc | Low-voc polyamino alcohols |
US10563042B2 (en) | 2016-12-14 | 2020-02-18 | Ecolab Usa Inc. | Quaternary cationic polymers |
US11427964B2 (en) | 2018-06-12 | 2022-08-30 | Ecolab Usa Inc. | Quaternary cationic surfactants and polymers for use as release and coating modifying agents in creping and tissue papers |
Family Cites Families (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2046720A (en) * | 1933-06-09 | 1936-07-07 | Girdler Corp | Nu-hydroxy-aminoalkyl substituted alkylene diamines |
US20060106129A1 (en) * | 2002-05-08 | 2006-05-18 | Michael Gernon | Optimized alkanolamines for latex paints |
US20100041801A1 (en) * | 2007-01-05 | 2010-02-18 | Dowling Conor M | Amine neutralizing agents for low volatile compound organic paints |
JP5698218B2 (ja) * | 2009-04-29 | 2015-04-08 | アンガス ケミカル カンパニー | ペイント及びコーティング用の低voc添加剤としての第三級アミノアルコール |
WO2010126962A1 (en) * | 2009-04-29 | 2010-11-04 | Dow Global Technologies Inc. | Polyhydroxy-diamines as multi-functional additives for paints, coatings and expoxies |
CN102803202B (zh) * | 2009-06-26 | 2014-05-28 | 安格斯化学公司 | 作为用于油漆和涂料的低气味、低voc多官能添加剂的多羟基二胺 |
US8722936B2 (en) * | 2009-10-08 | 2014-05-13 | Angus Chemical Company | Low-VOC polyamines |
CA2759346C (en) * | 2010-12-27 | 2014-01-28 | Dow Global Technologies Llc | Low-voc polyamino alcohols |
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2011
- 2011-11-22 CA CA2759341A patent/CA2759341C/en active Active
- 2011-11-22 JP JP2011254494A patent/JP5551673B2/ja active Active
- 2011-11-23 EP EP11190347.2A patent/EP2468713B1/en active Active
- 2011-12-13 US US13/323,920 patent/US8288464B2/en active Active
- 2011-12-21 CN CN201110452598.4A patent/CN102584607B/zh active Active
- 2011-12-26 BR BRPI1107063-3A patent/BRPI1107063B1/pt active IP Right Grant
Also Published As
Publication number | Publication date |
---|---|
CN102584607A (zh) | 2012-07-18 |
EP2468713A1 (en) | 2012-06-27 |
US20120165463A1 (en) | 2012-06-28 |
BRPI1107063B1 (pt) | 2019-02-12 |
CN102584607B (zh) | 2015-06-10 |
US8288464B2 (en) | 2012-10-16 |
EP2468713B1 (en) | 2016-03-16 |
CA2759341A1 (en) | 2012-06-27 |
JP2012136508A (ja) | 2012-07-19 |
BRPI1107063A2 (pt) | 2013-06-11 |
CA2759341C (en) | 2013-11-19 |
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