JPS6145650B2 - - Google Patents
Info
- Publication number
- JPS6145650B2 JPS6145650B2 JP8718377A JP8718377A JPS6145650B2 JP S6145650 B2 JPS6145650 B2 JP S6145650B2 JP 8718377 A JP8718377 A JP 8718377A JP 8718377 A JP8718377 A JP 8718377A JP S6145650 B2 JPS6145650 B2 JP S6145650B2
- Authority
- JP
- Japan
- Prior art keywords
- hydrogen atom
- alkali metal
- atom
- formula
- carbon atoms
- 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.)
- Expired
Links
- 229920000642 polymer Polymers 0.000 claims description 24
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 13
- 229910052783 alkali metal Inorganic materials 0.000 claims description 9
- 125000000217 alkyl group Chemical group 0.000 claims description 9
- 125000004432 carbon atom Chemical group C* 0.000 claims description 9
- 150000001340 alkali metals Chemical group 0.000 claims description 8
- 125000005843 halogen group Chemical group 0.000 claims description 5
- 239000003505 polymerization initiator Substances 0.000 claims description 4
- 150000008044 alkali metal hydroxides Chemical class 0.000 claims description 3
- 150000001413 amino acids Chemical class 0.000 claims description 3
- 239000002280 amphoteric surfactant Substances 0.000 claims description 3
- 238000004519 manufacturing process Methods 0.000 claims description 2
- 239000003513 alkali Chemical group 0.000 claims 1
- 150000001875 compounds Chemical class 0.000 description 24
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 18
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 12
- 239000007864 aqueous solution Substances 0.000 description 11
- 238000007127 saponification reaction Methods 0.000 description 10
- 238000006243 chemical reaction Methods 0.000 description 5
- 238000006116 polymerization reaction Methods 0.000 description 5
- 239000004094 surface-active agent Substances 0.000 description 5
- NOWKCMXCCJGMRR-UHFFFAOYSA-N Aziridine Chemical compound C1CN1 NOWKCMXCCJGMRR-UHFFFAOYSA-N 0.000 description 4
- 238000010521 absorption reaction Methods 0.000 description 4
- 150000002148 esters Chemical class 0.000 description 4
- 239000007787 solid Substances 0.000 description 4
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- 239000011734 sodium Substances 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- -1 acryl vinyl Chemical group 0.000 description 2
- 238000007259 addition reaction Methods 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 229940125904 compound 1 Drugs 0.000 description 2
- 238000000921 elemental analysis Methods 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 238000010528 free radical solution polymerization reaction Methods 0.000 description 2
- 239000005457 ice water Substances 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 239000000178 monomer Substances 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- 239000004902 Softening Agent Substances 0.000 description 1
- 238000000862 absorption spectrum Methods 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 239000002216 antistatic agent Substances 0.000 description 1
- 238000005452 bending Methods 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000012662 bulk polymerization Methods 0.000 description 1
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 238000010538 cationic polymerization reaction Methods 0.000 description 1
- 229940125782 compound 2 Drugs 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 125000002704 decyl 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])* 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- VEUUMBGHMNQHGO-UHFFFAOYSA-N ethyl chloroacetate Chemical compound CCOC(=O)CCl VEUUMBGHMNQHGO-UHFFFAOYSA-N 0.000 description 1
- 238000005187 foaming Methods 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 229910000000 metal hydroxide Inorganic materials 0.000 description 1
- 150000004692 metal hydroxides Chemical class 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- QABLOFMHHSOFRJ-UHFFFAOYSA-N methyl 2-chloroacetate Chemical compound COC(=O)CCl QABLOFMHHSOFRJ-UHFFFAOYSA-N 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 239000012454 non-polar solvent Substances 0.000 description 1
- 125000002524 organometallic group Chemical group 0.000 description 1
- VWSUVZVPDQDVRT-UHFFFAOYSA-N phenylperoxybenzene Chemical compound C=1C=CC=CC=1OOC1=CC=CC=C1 VWSUVZVPDQDVRT-UHFFFAOYSA-N 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 239000002798 polar solvent Substances 0.000 description 1
- 239000002685 polymerization catalyst Substances 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 238000010526 radical polymerization reaction Methods 0.000 description 1
- 238000007151 ring opening polymerisation reaction Methods 0.000 description 1
- 239000002453 shampoo Substances 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- VOITXYVAKOUIBA-UHFFFAOYSA-N triethylaluminium Chemical compound CC[Al](CC)CC VOITXYVAKOUIBA-UHFFFAOYSA-N 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
Landscapes
- Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)
- Detergent Compositions (AREA)
- Polymers With Sulfur, Phosphorus Or Metals In The Main Chain (AREA)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP8718377A JPS5421500A (en) | 1977-07-20 | 1977-07-20 | Ampho high polymer* preparation thereof and amino acid type amphoteric surfactant composed thereof |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP8718377A JPS5421500A (en) | 1977-07-20 | 1977-07-20 | Ampho high polymer* preparation thereof and amino acid type amphoteric surfactant composed thereof |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5421500A JPS5421500A (en) | 1979-02-17 |
| JPS6145650B2 true JPS6145650B2 (enExample) | 1986-10-09 |
Family
ID=13907863
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP8718377A Granted JPS5421500A (en) | 1977-07-20 | 1977-07-20 | Ampho high polymer* preparation thereof and amino acid type amphoteric surfactant composed thereof |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5421500A (enExample) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP4942284B2 (ja) * | 2003-09-26 | 2012-05-30 | 株式会社日本触媒 | ポリアルキレンイミン誘導体およびその用途 |
| JP2010001495A (ja) * | 2009-09-29 | 2010-01-07 | Nippon Shokubai Co Ltd | ポリアルキレンイミン誘導体、その製造方法およびその用途 |
-
1977
- 1977-07-20 JP JP8718377A patent/JPS5421500A/ja active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5421500A (en) | 1979-02-17 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JPH0320331A (ja) | 溶剤可溶性ポリオルガノシルセスキオキサンの製造方法 | |
| Ali et al. | Cyclopolymerization studies of diallyl‐and tetraallylpiperazinium salts | |
| CN103467742B (zh) | 聚乙烯撑硫化物及其制备方法 | |
| EP0530408B1 (en) | Olefin polymers having both ends modified and processes for the production thereof | |
| JPH09227688A (ja) | ヒドロキシル基含有シロキサン化合物の製造方法 | |
| JP2862336B2 (ja) | 両末端修飾オレフィン重合体及びその製造法 | |
| JP5000904B2 (ja) | 末端にメルカプト基を有するポリビニルアルコール系重合体の製造方法 | |
| JP3078060B2 (ja) | 星型ブロック共重合体およびその製造方法 | |
| JPH082923B2 (ja) | 星型化合物の製造方法 | |
| JPH07258310A (ja) | アクリレート類の重合を制御する方法及び触媒 | |
| JP3912457B2 (ja) | プロピレンオキシドの重合触媒組成物 | |
| US3202716A (en) | Monomeric derivatives of 2, 4-dihydroxybenzophenone | |
| JP2004514768A (ja) | 高分子量パーフルオロシクロブタンポリマーおよびその製造方法 | |
| JP7587212B2 (ja) | スルフィド基を有するアリル位置換メタクリル酸エステルの製造方法 | |
| JP3630858B2 (ja) | ブロック共重合体 | |
| JP7441526B2 (ja) | 架橋高分子化合物およびその製造方法並びに高分子化合物の生成方法 | |
| US3156720A (en) | Ethylenically unsaturated derivatives of ortho-dihydric phenols | |
| JPH0469141B2 (enExample) | ||
| JPS6251943B2 (enExample) | ||
| JP3807455B2 (ja) | ポリ（アリルトリアルキルアンモニウム塩）の製造方法 | |
| JP3078061B2 (ja) | 水酸基を有する星型化合物の製造方法 | |
| JP2575805B2 (ja) | 含フッ素フェネチルアルコール誘導体 | |
| JPH05279414A (ja) | 星型ポリビニルアセタールおよびその製造方法 | |
| JPS63162640A (ja) | ペンタエリスリト−ルアリルエ−テルの製造方法 | |
| JPS63260925A (ja) | 主鎖にジシラン結合を有するポリシロキサンおよびその製造法 |