JP2014132077A5 - - Google Patents
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- Publication number
- JP2014132077A5 JP2014132077A5 JP2013263667A JP2013263667A JP2014132077A5 JP 2014132077 A5 JP2014132077 A5 JP 2014132077A5 JP 2013263667 A JP2013263667 A JP 2013263667A JP 2013263667 A JP2013263667 A JP 2013263667A JP 2014132077 A5 JP2014132077 A5 JP 2014132077A5
- Authority
- JP
- Japan
- Prior art keywords
- polyethylene glycol
- molecular weight
- high molecular
- weight polyethylene
- group
- 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
- 229920001223 polyethylene glycol Polymers 0.000 claims description 33
- 238000000034 method Methods 0.000 claims description 32
- 150000001875 compounds Chemical class 0.000 claims description 30
- 239000004705 High-molecular-weight polyethylene Substances 0.000 claims description 25
- 239000003960 organic solvent Substances 0.000 claims description 21
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 20
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 claims description 12
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims description 12
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims description 12
- 238000000926 separation method Methods 0.000 claims description 12
- 239000002904 solvent Substances 0.000 claims description 12
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 10
- 229910017053 inorganic salt Inorganic materials 0.000 claims description 10
- 150000003839 salts Chemical class 0.000 claims description 10
- 239000012044 organic layer Substances 0.000 claims description 9
- 239000002202 Polyethylene glycol Substances 0.000 claims description 8
- 239000000654 additive Substances 0.000 claims description 8
- 230000000996 additive effect Effects 0.000 claims description 8
- 125000000524 functional group Chemical group 0.000 claims description 8
- 239000010410 layer Substances 0.000 claims description 8
- 101000629400 Homo sapiens Mesoderm-specific transcript homolog protein Proteins 0.000 claims description 7
- 102100026821 Mesoderm-specific transcript homolog protein Human genes 0.000 claims description 7
- KXSKAZFMTGADIV-UHFFFAOYSA-N 2-[3-(2-hydroxyethoxy)propoxy]ethanol Chemical compound OCCOCCCOCCO KXSKAZFMTGADIV-UHFFFAOYSA-N 0.000 claims description 6
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 claims description 6
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 6
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical group C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims description 6
- 101000693243 Homo sapiens Paternally-expressed gene 3 protein Proteins 0.000 claims description 6
- 102100025757 Paternally-expressed gene 3 protein Human genes 0.000 claims description 6
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 claims description 6
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 4
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 claims description 4
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 claims description 4
- BZLVMXJERCGZMT-UHFFFAOYSA-N Methyl tert-butyl ether Chemical compound COC(C)(C)C BZLVMXJERCGZMT-UHFFFAOYSA-N 0.000 claims description 4
- -1 PEG2 Proteins 0.000 claims description 4
- DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 claims description 4
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 claims description 4
- 229910052783 alkali metal Inorganic materials 0.000 claims description 4
- 150000001340 alkali metals Chemical class 0.000 claims description 4
- 229910052799 carbon Inorganic materials 0.000 claims description 4
- 125000004432 carbon atom Chemical group C* 0.000 claims description 4
- 239000012535 impurity Substances 0.000 claims description 4
- 125000006239 protecting group Chemical group 0.000 claims description 4
- DKPFZGUDAPQIHT-UHFFFAOYSA-N Butyl acetate Natural products CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 claims description 2
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 claims description 2
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 claims description 2
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 claims description 2
- KXKVLQRXCPHEJC-UHFFFAOYSA-N acetic acid trimethyl ester Natural products COC(C)=O KXKVLQRXCPHEJC-UHFFFAOYSA-N 0.000 claims description 2
- 238000001994 activation Methods 0.000 claims description 2
- 150000004945 aromatic hydrocarbons Chemical class 0.000 claims description 2
- 125000004429 atom Chemical group 0.000 claims description 2
- 239000007857 degradation product Substances 0.000 claims description 2
- 125000003827 glycol group Chemical group 0.000 claims description 2
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 claims description 2
- 150000002430 hydrocarbons Chemical group 0.000 claims description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 2
- 239000000203 mixture Substances 0.000 claims description 2
- 238000006116 polymerization reaction Methods 0.000 claims description 2
- 238000000746 purification Methods 0.000 claims description 2
- 239000007858 starting material Substances 0.000 claims description 2
- 150000003462 sulfoxides Chemical class 0.000 claims description 2
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 claims description 2
- 125000003944 tolyl group Chemical group 0.000 claims description 2
- 239000008096 xylene Substances 0.000 claims description 2
- 229920000642 polymer Polymers 0.000 claims 1
- YIWGJFPJRAEKMK-UHFFFAOYSA-N 1-(2H-benzotriazol-5-yl)-3-methyl-8-[2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidine-5-carbonyl]-1,3,8-triazaspiro[4.5]decane-2,4-dione Chemical compound CN1C(=O)N(c2ccc3n[nH]nc3c2)C2(CCN(CC2)C(=O)c2cnc(NCc3cccc(OC(F)(F)F)c3)nc2)C1=O YIWGJFPJRAEKMK-UHFFFAOYSA-N 0.000 description 1
- FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 description 1
- 150000002009 diols Chemical class 0.000 description 1
- 239000000047 product Substances 0.000 description 1
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2013263667A JP5843172B2 (ja) | 2009-03-31 | 2013-12-20 | 高分子量ポリエチレングリコール化合物の精製方法 |
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2009084773 | 2009-03-31 | ||
| JP2009084773 | 2009-03-31 | ||
| JP2013263667A JP5843172B2 (ja) | 2009-03-31 | 2013-12-20 | 高分子量ポリエチレングリコール化合物の精製方法 |
Related Parent Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2010078127A Division JP5569787B2 (ja) | 2009-03-31 | 2010-03-30 | 高分子量ポリエチレングリコール化合物の精製方法 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2014132077A JP2014132077A (ja) | 2014-07-17 |
| JP2014132077A5 true JP2014132077A5 (enExample) | 2014-08-28 |
| JP5843172B2 JP5843172B2 (ja) | 2016-01-13 |
Family
ID=43069052
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2010078127A Active JP5569787B2 (ja) | 2009-03-31 | 2010-03-30 | 高分子量ポリエチレングリコール化合物の精製方法 |
| JP2013263667A Active JP5843172B2 (ja) | 2009-03-31 | 2013-12-20 | 高分子量ポリエチレングリコール化合物の精製方法 |
Family Applications Before (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2010078127A Active JP5569787B2 (ja) | 2009-03-31 | 2010-03-30 | 高分子量ポリエチレングリコール化合物の精製方法 |
Country Status (2)
| Country | Link |
|---|---|
| US (1) | US20100292515A1 (enExample) |
| JP (2) | JP5569787B2 (enExample) |
Families Citing this family (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8163869B1 (en) | 2010-12-27 | 2012-04-24 | Nof Corporation | Purification method of carboxyl group-containing polyoxyethylene derivative |
| US9458292B2 (en) | 2013-03-27 | 2016-10-04 | Nof Corporation | Method for purifying polyethylene glycol having one amino group |
| JP6366382B2 (ja) * | 2014-06-27 | 2018-08-01 | キヤノン株式会社 | トナーの製造方法 |
| JP6935059B2 (ja) * | 2017-03-30 | 2021-09-15 | 日油株式会社 | カルボキシル基を一つ有するポリエチレングリコールの精製方法 |
| DE102018000650A1 (de) * | 2018-01-27 | 2019-08-01 | Friedrich-Schiller-Universität Jena | Verfahren zur Bestimmung von Verunreinigungen in Polyalkylenethern oder Polyalkylenaminen und dessen Verwendung |
| CN111936549B (zh) * | 2018-03-29 | 2023-03-10 | 日油株式会社 | 包含三苯甲基的单分散聚乙二醇的纯化方法 |
| CN109909464B (zh) * | 2019-04-11 | 2020-10-16 | 东北大学 | 一种具有骨架结构的高透磁高导热结晶器内套 |
| JP7688818B2 (ja) * | 2019-12-27 | 2025-06-05 | 日油株式会社 | 分岐型ポリエチレングリコールの精製方法 |
| CN111579660A (zh) * | 2020-04-24 | 2020-08-25 | 药源生物科技（启东）有限公司 | 一种测定聚乙二醇4000及其散剂平均分子量及分布系数的检测方法 |
| CN115160558B (zh) * | 2022-07-27 | 2023-06-02 | 江西阿尔法高科药业有限公司 | 一种药用辅料级聚氧乙烯的精制方法 |
Family Cites Families (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3492358A (en) * | 1968-04-10 | 1970-01-27 | Dow Chemical Co | Purification of ethers |
| JPS5432597A (en) * | 1977-08-18 | 1979-03-09 | Kanegafuchi Chem Ind Co Ltd | Purification of high molecular weight alkylene oxide polymer |
| DE2854541A1 (de) * | 1978-12-16 | 1980-06-26 | Bayer Ag | Verfahren zur reinigung nichtionischer emulgatoren |
| US4962238A (en) * | 1989-10-04 | 1990-10-09 | Exxon Research And Engineering Company | Removal of glycols from a polyalkylene glycol dialkyl ether solution |
| DE3933333A1 (de) * | 1989-10-06 | 1991-04-11 | Basf Ag | Verfahren zur reinigung von polyalkylenetherglykolen, die heteropolysaeuren enthalten |
| US5298410A (en) * | 1993-02-25 | 1994-03-29 | Sterling Winthrop Inc. | Lyophilized formulation of polyethylene oxide modified proteins with increased shelf-life |
| US5932462A (en) * | 1995-01-10 | 1999-08-03 | Shearwater Polymers, Inc. | Multiarmed, monofunctional, polymer for coupling to molecules and surfaces |
| JPH09169683A (ja) * | 1995-12-20 | 1997-06-30 | Denki Kagaku Kogyo Kk | ポリオキシアルキレン誘導体の精製方法 |
| US5800711A (en) * | 1996-10-18 | 1998-09-01 | Mdv Technologies, Inc. | Process for the fractionation of polyoxyalkylene block copolymers |
| US6455639B1 (en) * | 1998-03-24 | 2002-09-24 | Nof Corporation | Oxirane derivative and process for the preparation thereof |
| JP4123856B2 (ja) * | 2001-07-31 | 2008-07-23 | 日油株式会社 | 生体関連物質の修飾剤およびポリオキシアルキレン誘導体の製造方法 |
| JP4412461B2 (ja) * | 2002-11-20 | 2010-02-10 | 日油株式会社 | 修飾された生体関連物質、その製造方法および中間体 |
| US8367876B2 (en) * | 2004-07-13 | 2013-02-05 | Kaneka Corporation | Method for producing polyether |
| US20060045866A1 (en) * | 2004-09-01 | 2006-03-02 | Chris Chappelow | Novel high purity and high molecular weight mPEG alcohol compositions |
| US7199193B2 (en) * | 2004-09-28 | 2007-04-03 | Dow Global Technologies, Inc. | Polyethylene glycol compounds and process of making |
-
2010
- 2010-03-30 JP JP2010078127A patent/JP5569787B2/ja active Active
- 2010-03-31 US US12/751,195 patent/US20100292515A1/en not_active Abandoned
-
2013
- 2013-12-20 JP JP2013263667A patent/JP5843172B2/ja active Active
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