JPS60158202A - 分離剤 - Google Patents
分離剤Info
- Publication number
- JPS60158202A JPS60158202A JP59014957A JP1495784A JPS60158202A JP S60158202 A JPS60158202 A JP S60158202A JP 59014957 A JP59014957 A JP 59014957A JP 1495784 A JP1495784 A JP 1495784A JP S60158202 A JPS60158202 A JP S60158202A
- Authority
- JP
- Japan
- Prior art keywords
- glycidyl methacrylate
- amino acid
- methanol
- optically active
- resolving agent
- 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
- 150000001413 amino acids Chemical class 0.000 claims abstract description 27
- VOZRXNHHFUQHIL-UHFFFAOYSA-N glycidyl methacrylate Chemical compound CC(=C)C(=O)OCC1CO1 VOZRXNHHFUQHIL-UHFFFAOYSA-N 0.000 claims abstract description 24
- 229910052751 metal Inorganic materials 0.000 claims abstract description 12
- 239000002184 metal Substances 0.000 claims abstract description 12
- 229920001577 copolymer Polymers 0.000 claims abstract description 9
- 150000003839 salts Chemical class 0.000 claims abstract description 9
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 7
- 125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 claims abstract description 5
- 229940024606 amino acid Drugs 0.000 abstract description 26
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 abstract description 13
- 239000000741 silica gel Substances 0.000 abstract description 12
- 229910002027 silica gel Inorganic materials 0.000 abstract description 12
- 230000003287 optical effect Effects 0.000 abstract description 11
- 229960002429 proline Drugs 0.000 abstract description 11
- ONIBWKKTOPOVIA-BYPYZUCNSA-N L-Proline Chemical compound OC(=O)[C@@H]1CCCN1 ONIBWKKTOPOVIA-BYPYZUCNSA-N 0.000 abstract description 10
- 229930182821 L-proline Natural products 0.000 abstract description 10
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 abstract description 10
- 239000000178 monomer Substances 0.000 abstract description 9
- 239000002904 solvent Substances 0.000 abstract description 9
- 159000000000 sodium salts Chemical class 0.000 abstract description 7
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 abstract description 4
- 238000012856 packing Methods 0.000 abstract description 4
- 238000004811 liquid chromatography Methods 0.000 abstract description 3
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 66
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 25
- 239000000945 filler Substances 0.000 description 19
- 229920000642 polymer Polymers 0.000 description 16
- OZAIFHULBGXAKX-UHFFFAOYSA-N 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile Chemical compound N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 description 14
- 230000015572 biosynthetic process Effects 0.000 description 14
- 238000003786 synthesis reaction Methods 0.000 description 14
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 14
- 229910000365 copper sulfate Inorganic materials 0.000 description 11
- ARUVKPQLZAKDPS-UHFFFAOYSA-L copper(II) sulfate Chemical compound [Cu+2].[O-][S+2]([O-])([O-])[O-] ARUVKPQLZAKDPS-UHFFFAOYSA-L 0.000 description 11
- 239000000203 mixture Substances 0.000 description 9
- 239000003480 eluent Substances 0.000 description 8
- 239000003999 initiator Substances 0.000 description 8
- 238000000926 separation method Methods 0.000 description 8
- 239000007864 aqueous solution Substances 0.000 description 7
- 150000001879 copper Chemical class 0.000 description 7
- AHUXYBVKTIBBJW-UHFFFAOYSA-N dimethoxy(diphenyl)silane Chemical compound C=1C=CC=CC=1[Si](OC)(OC)C1=CC=CC=C1 AHUXYBVKTIBBJW-UHFFFAOYSA-N 0.000 description 7
- 238000000034 method Methods 0.000 description 7
- 239000002245 particle Substances 0.000 description 7
- 239000011148 porous material Substances 0.000 description 7
- -1 silane compound Chemical class 0.000 description 7
- 239000007787 solid Substances 0.000 description 7
- 229910001220 stainless steel Inorganic materials 0.000 description 7
- 239000010935 stainless steel Substances 0.000 description 7
- 238000005406 washing Methods 0.000 description 7
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 6
- 229910000077 silane Inorganic materials 0.000 description 4
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 4
- 229920002554 vinyl polymer Polymers 0.000 description 4
- SOGAXMICEFXMKE-UHFFFAOYSA-N Butylmethacrylate Chemical compound CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 description 3
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 3
- 229910000831 Steel Inorganic materials 0.000 description 3
- 229920002401 polyacrylamide Polymers 0.000 description 3
- 239000010959 steel Substances 0.000 description 3
- JLBJTVDPSNHSKJ-UHFFFAOYSA-N 4-Methylstyrene Chemical compound CC1=CC=C(C=C)C=C1 JLBJTVDPSNHSKJ-UHFFFAOYSA-N 0.000 description 2
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 2
- 239000004793 Polystyrene Substances 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 239000000499 gel Substances 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 239000012046 mixed solvent Substances 0.000 description 2
- 229920002223 polystyrene Polymers 0.000 description 2
- KFDVPJUYSDEJTH-UHFFFAOYSA-N 4-ethenylpyridine Chemical compound C=CC1=CC=NC=C1 KFDVPJUYSDEJTH-UHFFFAOYSA-N 0.000 description 1
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- PMMYEEVYMWASQN-DMTCNVIQSA-N Hydroxyproline Chemical compound O[C@H]1CN[C@H](C(O)=O)C1 PMMYEEVYMWASQN-DMTCNVIQSA-N 0.000 description 1
- 125000000174 L-prolyl group Chemical group [H]N1C([H])([H])C([H])([H])C([H])([H])[C@@]1([H])C(*)=O 0.000 description 1
- 101100010166 Mus musculus Dok3 gene Proteins 0.000 description 1
- ONIBWKKTOPOVIA-UHFFFAOYSA-N Proline Natural products OC(=O)C1CCCN1 ONIBWKKTOPOVIA-UHFFFAOYSA-N 0.000 description 1
- 125000005396 acrylic acid ester group Chemical group 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 1
- 150000001342 alkaline earth metals Chemical class 0.000 description 1
- 150000003862 amino acid derivatives Chemical class 0.000 description 1
- 239000011324 bead Substances 0.000 description 1
- KVNRLNFWIYMESJ-UHFFFAOYSA-N butyronitrile Chemical compound CCCC#N KVNRLNFWIYMESJ-UHFFFAOYSA-N 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 238000007334 copolymerization reaction Methods 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- PMMYEEVYMWASQN-UHFFFAOYSA-N dl-hydroxyproline Natural products OC1C[NH2+]C(C([O-])=O)C1 PMMYEEVYMWASQN-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 150000004795 grignard reagents Chemical class 0.000 description 1
- 238000004128 high performance liquid chromatography Methods 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 230000003301 hydrolyzing effect Effects 0.000 description 1
- 229960002591 hydroxyproline Drugs 0.000 description 1
- 150000002484 inorganic compounds Chemical class 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 238000012690 ionic polymerization Methods 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- FQPSGWSUVKBHSU-UHFFFAOYSA-N methacrylamide Chemical compound CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 description 1
- 150000004702 methyl esters Chemical class 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 238000010526 radical polymerization reaction Methods 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- FGMPLJWBKKVCDB-UHFFFAOYSA-N trans-L-hydroxy-proline Natural products ON1CCCC1C(O)=O FGMPLJWBKKVCDB-UHFFFAOYSA-N 0.000 description 1
- 229910052723 transition metal Inorganic materials 0.000 description 1
- 150000003624 transition metals Chemical class 0.000 description 1
- 230000004304 visual acuity Effects 0.000 description 1
Landscapes
- Solid-Sorbent Or Filter-Aiding Compositions (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP59014957A JPS60158202A (ja) | 1984-01-30 | 1984-01-30 | 分離剤 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP59014957A JPS60158202A (ja) | 1984-01-30 | 1984-01-30 | 分離剤 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS60158202A true JPS60158202A (ja) | 1985-08-19 |
| JPH0475209B2 JPH0475209B2 (enExample) | 1992-11-30 |
Family
ID=11875454
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP59014957A Granted JPS60158202A (ja) | 1984-01-30 | 1984-01-30 | 分離剤 |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS60158202A (enExample) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2003002812A (ja) * | 2001-04-19 | 2003-01-08 | Toho Chem Ind Co Ltd | アミノ酸変性水溶性高分子を含む化粧料組成物 |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5914958A (ja) * | 1982-07-15 | 1984-01-25 | Komori Printing Mach Co Ltd | 輪転印刷機の刷版装着装置 |
-
1984
- 1984-01-30 JP JP59014957A patent/JPS60158202A/ja active Granted
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5914958A (ja) * | 1982-07-15 | 1984-01-25 | Komori Printing Mach Co Ltd | 輪転印刷機の刷版装着装置 |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2003002812A (ja) * | 2001-04-19 | 2003-01-08 | Toho Chem Ind Co Ltd | アミノ酸変性水溶性高分子を含む化粧料組成物 |
Also Published As
| Publication number | Publication date |
|---|---|
| JPH0475209B2 (enExample) | 1992-11-30 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US5968652A (en) | Silane coated particle | |
| KR101354476B1 (ko) | 크로마토그래피 매질 성능을 향상시키기 위한 그라프팅 방법 | |
| JP3147389B2 (ja) | アニオン交換体 | |
| CN104109222B (zh) | 一种含多面体寡聚倍半硅烷试剂的杂化整体材料的制备 | |
| CN105992949A (zh) | 固相载体、固相载体的制造方法、亲和精制用载体、亲和色谱用填充剂的制造方法、亲和色谱用填充剂、色谱柱和精制方法 | |
| US5925253A (en) | Hydrolytically stable resins for use in anion-exchange chromatography | |
| CN105348541B (zh) | 血液净化吸附剂及其制备方法 | |
| JPS58132004A (ja) | 親水性重合体マトリツクスを有する両性イオン交換体の製造方法 | |
| KR20120031869A (ko) | 개선된 크로마토그래피 매질의 제조방법 및 사용방법 | |
| JPH0647454B2 (ja) | アシル化ポリエチレンイミン結合相シリカ生成物のスルホン酸誘導体類 | |
| EP0068290B1 (en) | Optically active polymers of methacrylate esters | |
| WO2001096424A1 (en) | Process for producing high-purity vinylpyrrolidone polymer | |
| JPS60158202A (ja) | 分離剤 | |
| JPH0691956B2 (ja) | 光学活性な高分子を担持させた分離用吸着剤 | |
| JPH09503865A (ja) | ゲル浸透クロマトグラフィーの方法と保持体 | |
| JPH02104289A (ja) | 新しい着色したモノマー及びポリマー、該ポリマーの製造方法並びに該ポリマーを使用して生物学的に活性な物質を分離する方法 | |
| JPS60158203A (ja) | 分離剤 | |
| JP3543476B2 (ja) | 架橋共重合体の製造方法 | |
| JP3147943B2 (ja) | 糖液精製用架橋アニオン交換体 | |
| EP0444643A2 (en) | Anion exchanger | |
| JPS62227446A (ja) | アフイニテイ・クロマトグラフイ−用吸着体 | |
| JP2006122851A (ja) | ポリマー結合型カラム | |
| JPS6069111A (ja) | 2−ピリジル基を有する有機重合体 | |
| JP3259728B2 (ja) | アニオン交換体の製造方法 | |
| JPS61162750A (ja) | 光学分割用充填剤 |