JPS6164325A - 変性ポリアミン - Google Patents
変性ポリアミンInfo
- Publication number
- JPS6164325A JPS6164325A JP59184695A JP18469584A JPS6164325A JP S6164325 A JPS6164325 A JP S6164325A JP 59184695 A JP59184695 A JP 59184695A JP 18469584 A JP18469584 A JP 18469584A JP S6164325 A JPS6164325 A JP S6164325A
- Authority
- JP
- Japan
- Prior art keywords
- polyamine
- glycidyl ether
- ether
- derivative
- modified
- 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
- 229920000768 polyamine Polymers 0.000 title claims abstract description 56
- 150000001875 compounds Chemical class 0.000 claims abstract description 25
- 125000001183 hydrocarbyl group Chemical group 0.000 claims abstract description 3
- 239000002904 solvent Substances 0.000 claims description 8
- 125000004432 carbon atom Chemical group C* 0.000 claims description 6
- 239000000126 substance Substances 0.000 claims description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract description 3
- 239000001257 hydrogen Substances 0.000 abstract description 3
- 229910052739 hydrogen Inorganic materials 0.000 abstract description 3
- 150000001412 amines Chemical class 0.000 abstract 1
- -1 alkylene imine Chemical class 0.000 description 50
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 10
- 125000000217 alkyl group Chemical group 0.000 description 10
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 8
- 229920002873 Polyethylenimine Polymers 0.000 description 8
- 229920005989 resin Polymers 0.000 description 8
- 239000011347 resin Substances 0.000 description 8
- 241000238557 Decapoda Species 0.000 description 7
- 238000006243 chemical reaction Methods 0.000 description 7
- 239000004952 Polyamide Substances 0.000 description 6
- 239000003795 chemical substances by application Substances 0.000 description 6
- 239000000203 mixture Substances 0.000 description 6
- 229920002647 polyamide Polymers 0.000 description 6
- 238000007720 emulsion polymerization reaction Methods 0.000 description 5
- 150000003944 halohydrins Chemical class 0.000 description 5
- GQWWGRUJOCIUKI-UHFFFAOYSA-N 2-[3-(2-methyl-1-oxopyrrolo[1,2-a]pyrazin-3-yl)propyl]guanidine Chemical compound O=C1N(C)C(CCCN=C(N)N)=CN2C=CC=C21 GQWWGRUJOCIUKI-UHFFFAOYSA-N 0.000 description 4
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 4
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 4
- 125000002947 alkylene group Chemical group 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
- GYZLOYUZLJXAJU-UHFFFAOYSA-N diglycidyl ether Chemical class C1OC1COCC1CO1 GYZLOYUZLJXAJU-UHFFFAOYSA-N 0.000 description 4
- 239000000839 emulsion Substances 0.000 description 4
- 125000003700 epoxy group Chemical group 0.000 description 4
- 239000004094 surface-active agent Substances 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- 239000007864 aqueous solution Substances 0.000 description 3
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 3
- 239000007795 chemical reaction product Substances 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 239000003995 emulsifying agent Substances 0.000 description 3
- 150000002118 epoxides Chemical class 0.000 description 3
- 125000001165 hydrophobic group Chemical group 0.000 description 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 3
- 239000004711 α-olefin Substances 0.000 description 3
- 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
- 239000000853 adhesive Substances 0.000 description 2
- 230000001070 adhesive effect Effects 0.000 description 2
- 235000011037 adipic acid Nutrition 0.000 description 2
- 239000001361 adipic acid Substances 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 238000009833 condensation Methods 0.000 description 2
- 230000005494 condensation Effects 0.000 description 2
- 238000007334 copolymerization reaction Methods 0.000 description 2
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
- 239000000835 fiber Substances 0.000 description 2
- 150000002466 imines Chemical class 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 229920001281 polyalkylene Polymers 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- 150000003333 secondary alcohols Chemical class 0.000 description 2
- 238000004513 sizing Methods 0.000 description 2
- 125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([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 2
- 238000003756 stirring Methods 0.000 description 2
- VILCJCGEZXAXTO-UHFFFAOYSA-N 2,2,2-tetramine Chemical compound NCCNCCNCCN VILCJCGEZXAXTO-UHFFFAOYSA-N 0.000 description 1
- BBBUAWSVILPJLL-UHFFFAOYSA-N 2-(2-ethylhexoxymethyl)oxirane Chemical compound CCCCC(CC)COCC1CO1 BBBUAWSVILPJLL-UHFFFAOYSA-N 0.000 description 1
- XNJDQHLXEBQMDE-UHFFFAOYSA-N 2-(cyclohexyloxymethyl)oxirane Chemical compound C1OC1COC1CCCCC1 XNJDQHLXEBQMDE-UHFFFAOYSA-N 0.000 description 1
- MWEMVOWDVQAKHC-UHFFFAOYSA-N 2-(cyclopentyloxymethyl)oxirane Chemical compound C1OC1COC1CCCC1 MWEMVOWDVQAKHC-UHFFFAOYSA-N 0.000 description 1
- VMSIYTPWZLSMOH-UHFFFAOYSA-N 2-(dodecoxymethyl)oxirane Chemical compound CCCCCCCCCCCCOCC1CO1 VMSIYTPWZLSMOH-UHFFFAOYSA-N 0.000 description 1
- ZXJBWUAALADCRI-UHFFFAOYSA-N 2-(octadecoxymethyl)oxirane Chemical compound CCCCCCCCCCCCCCCCCCOCC1CO1 ZXJBWUAALADCRI-UHFFFAOYSA-N 0.000 description 1
- HRWYHCYGVIJOEC-UHFFFAOYSA-N 2-(octoxymethyl)oxirane Chemical compound CCCCCCCCOCC1CO1 HRWYHCYGVIJOEC-UHFFFAOYSA-N 0.000 description 1
- QNYBOILAKBSWFG-UHFFFAOYSA-N 2-(phenylmethoxymethyl)oxirane Chemical compound C1OC1COCC1=CC=CC=C1 QNYBOILAKBSWFG-UHFFFAOYSA-N 0.000 description 1
- SJLODCMGBPCIHA-UHFFFAOYSA-N 2-[1-cyclohexyl-1-[1-cyclohexyl-1-(oxiran-2-yl)decoxy]decyl]oxirane Chemical compound C1OC1C(C1CCCCC1)(CCCCCCCCC)OC(CCCCCCCCC)(C1CCCCC1)C1CO1 SJLODCMGBPCIHA-UHFFFAOYSA-N 0.000 description 1
- YWANOKMBEFRAJV-UHFFFAOYSA-N 2-[1-cyclohexyl-1-[1-cyclohexyl-1-(oxiran-2-yl)tridecoxy]tridecyl]oxirane Chemical compound C(CCCCCCCCCCC)C(C1CO1)(C1CCCCC1)OC(C1CO1)(CCCCCCCCCCCC)C1CCCCC1 YWANOKMBEFRAJV-UHFFFAOYSA-N 0.000 description 1
- VGWBCYJIAAOAKY-UHFFFAOYSA-N 2-[1-cyclopentyl-1-[1-cyclopentyl-1-(oxiran-2-yl)decoxy]decyl]oxirane Chemical compound C(CCCCCCCC)C(C1CO1)(C1CCCC1)OC(C1CO1)(CCCCCCCCC)C1CCCC1 VGWBCYJIAAOAKY-UHFFFAOYSA-N 0.000 description 1
- GNVLEDJRZZWPNZ-UHFFFAOYSA-N 2-[1-cyclopentyl-1-[1-cyclopentyl-1-(oxiran-2-yl)nonadecoxy]nonadecyl]oxirane Chemical compound C(CCCCCCCCCCCCCCCCC)C(C1CO1)(C1CCCC1)OC(C1CO1)(CCCCCCCCCCCCCCCCCC)C1CCCC1 GNVLEDJRZZWPNZ-UHFFFAOYSA-N 0.000 description 1
- NGCACSQHGAHCPN-UHFFFAOYSA-N 2-[1-cyclopentyl-1-[1-cyclopentyl-1-(oxiran-2-yl)tridecoxy]tridecyl]oxirane Chemical compound C(CCCCCCCCCCC)C(C1CO1)(C1CCCC1)OC(C1CO1)(CCCCCCCCCCCC)C1CCCC1 NGCACSQHGAHCPN-UHFFFAOYSA-N 0.000 description 1
- HQSSSDRMIQMATB-UHFFFAOYSA-N 2-[2-[2-(oxiran-2-yl)-1-phenylicosan-2-yl]oxy-1-phenylicosan-2-yl]oxirane Chemical compound C(CCCCCCCCCCCCCCCCC)C(C1CO1)(CC1=CC=CC=C1)OC(C1CO1)(CCCCCCCCCCCCCCCCCC)CC1=CC=CC=C1 HQSSSDRMIQMATB-UHFFFAOYSA-N 0.000 description 1
- OYABCAVFBBNKPR-UHFFFAOYSA-N 2-[2-[2-(oxiran-2-yl)-1-phenyltetradecan-2-yl]oxy-1-phenyltetradecan-2-yl]oxirane Chemical compound C(CCCCCCCCCCC)C(C1CO1)(CC1=CC=CC=C1)OC(C1CO1)(CCCCCCCCCCCC)CC1=CC=CC=C1 OYABCAVFBBNKPR-UHFFFAOYSA-N 0.000 description 1
- SYNNFKSHBFPYGR-UHFFFAOYSA-N 2-[2-[2-(oxiran-2-yl)-1-phenylundecan-2-yl]oxy-1-phenylundecan-2-yl]oxirane Chemical compound C(CCCCCCCC)C(C1CO1)(CC1=CC=CC=C1)OC(C1CO1)(CCCCCCCCC)CC1=CC=CC=C1 SYNNFKSHBFPYGR-UHFFFAOYSA-N 0.000 description 1
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- NOWKCMXCCJGMRR-UHFFFAOYSA-N Aziridine Chemical compound C1CN1 NOWKCMXCCJGMRR-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 1
- FQYUMYWMJTYZTK-UHFFFAOYSA-N Phenyl glycidyl ether Chemical compound C1OC1COC1=CC=CC=C1 FQYUMYWMJTYZTK-UHFFFAOYSA-N 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- 229920002396 Polyurea Polymers 0.000 description 1
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000008065 acid anhydrides Chemical class 0.000 description 1
- 238000007259 addition reaction Methods 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 125000003710 aryl alkyl group Chemical group 0.000 description 1
- 235000019445 benzyl alcohol Nutrition 0.000 description 1
- 150000003938 benzyl alcohols Chemical class 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 125000000753 cycloalkyl group Chemical group 0.000 description 1
- 230000018044 dehydration Effects 0.000 description 1
- 238000006297 dehydration reaction Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 230000001804 emulsifying effect Effects 0.000 description 1
- GKIPXFAANLTWBM-UHFFFAOYSA-N epibromohydrin Chemical compound BrCC1CO1 GKIPXFAANLTWBM-UHFFFAOYSA-N 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 239000012442 inert solvent Substances 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- LSHROXHEILXKHM-UHFFFAOYSA-N n'-[2-[2-[2-(2-aminoethylamino)ethylamino]ethylamino]ethyl]ethane-1,2-diamine Chemical compound NCCNCCNCCNCCNCCN LSHROXHEILXKHM-UHFFFAOYSA-N 0.000 description 1
- 125000004433 nitrogen atom Chemical group N* 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 150000007519 polyprotic acids Polymers 0.000 description 1
- 150000003141 primary amines Chemical class 0.000 description 1
- 229920013730 reactive polymer Polymers 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 239000012261 resinous substance Substances 0.000 description 1
- 150000003335 secondary amines Chemical group 0.000 description 1
- FAGUFWYHJQFNRV-UHFFFAOYSA-N tetraethylenepentamine Chemical compound NCCNCCNCCNCCN FAGUFWYHJQFNRV-UHFFFAOYSA-N 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
Landscapes
- Paper (AREA)
- Emulsifying, Dispersing, Foam-Producing Or Wetting Agents (AREA)
- Polyethers (AREA)
- Polymers With Sulfur, Phosphorus Or Metals In The Main Chain (AREA)
- Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP59184695A JPS6164325A (ja) | 1984-09-05 | 1984-09-05 | 変性ポリアミン |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP59184695A JPS6164325A (ja) | 1984-09-05 | 1984-09-05 | 変性ポリアミン |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS6164325A true JPS6164325A (ja) | 1986-04-02 |
| JPH0363575B2 JPH0363575B2 (enrdf_load_stackoverflow) | 1991-10-01 |
Family
ID=16157756
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP59184695A Granted JPS6164325A (ja) | 1984-09-05 | 1984-09-05 | 変性ポリアミン |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS6164325A (enrdf_load_stackoverflow) |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2004044015A (ja) * | 2002-07-11 | 2004-02-12 | Hymo Corp | 水溶性重合体分散液の使用方法 |
| JP2007056203A (ja) * | 2005-08-26 | 2007-03-08 | Dainippon Ink & Chem Inc | エポキシ主鎖とアルキレンイミン側鎖とを有する共重合体からなる顔料分散剤 |
| JP2012149185A (ja) * | 2011-01-20 | 2012-08-09 | Nippon Shokubai Co Ltd | ポリアルキレンアミンアルキレンオキシド共重合体 |
| JP2013060562A (ja) * | 2011-09-15 | 2013-04-04 | Nippon Shokubai Co Ltd | ポリアミン系重合体およびその製造方法 |
| WO2016039425A1 (ja) * | 2014-09-10 | 2016-03-17 | 株式会社日本触媒 | ポリアルキレンイミン誘導体を含む抗菌剤 |
-
1984
- 1984-09-05 JP JP59184695A patent/JPS6164325A/ja active Granted
Cited By (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2004044015A (ja) * | 2002-07-11 | 2004-02-12 | Hymo Corp | 水溶性重合体分散液の使用方法 |
| JP2007056203A (ja) * | 2005-08-26 | 2007-03-08 | Dainippon Ink & Chem Inc | エポキシ主鎖とアルキレンイミン側鎖とを有する共重合体からなる顔料分散剤 |
| JP2012149185A (ja) * | 2011-01-20 | 2012-08-09 | Nippon Shokubai Co Ltd | ポリアルキレンアミンアルキレンオキシド共重合体 |
| JP2013060562A (ja) * | 2011-09-15 | 2013-04-04 | Nippon Shokubai Co Ltd | ポリアミン系重合体およびその製造方法 |
| WO2016039425A1 (ja) * | 2014-09-10 | 2016-03-17 | 株式会社日本触媒 | ポリアルキレンイミン誘導体を含む抗菌剤 |
| JPWO2016039425A1 (ja) * | 2014-09-10 | 2017-04-27 | 株式会社日本触媒 | ポリアルキレンイミン誘導体を含む抗菌剤 |
| EP3202265A4 (en) * | 2014-09-10 | 2018-02-28 | Nippon Shokubai Co., Ltd. | Antimicrobial agent containing polyalkyleneimine derivative |
| US10905117B2 (en) | 2014-09-10 | 2021-02-02 | Nippon Shokubai Co., Ltd | Antimicrobial agent containing polyalkyleneimine derivative |
Also Published As
| Publication number | Publication date |
|---|---|
| JPH0363575B2 (enrdf_load_stackoverflow) | 1991-10-01 |
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