JPH029034B2 - - Google Patents

Info

Publication number: JPH029034B2
Authority: JP; Japan
Prior art keywords: ooc; formula; glycol; compound; pentaerythritol
Prior art date: 1987-03-23
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

Application number

JP6578187A

Other languages

English (en)

Japanese (ja)

Other versions

JPS62270591A (ja

Inventor

Seigo Oono

Tadao Nakaya

Minoru Imoto

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Oki Electric Industry Co Ltd

Original Assignee

Oki Electric Industry Co Ltd

Priority date (The priority date 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 date listed.)

1987-03-23

Filing date

1987-03-23

Publication date

1990-02-28

1987-03-23 Application filed by Oki Electric Industry Co Ltd filed Critical Oki Electric Industry Co Ltd

1987-03-23 Priority to JP6578187A priority Critical patent/JPS62270591A/ja

1987-11-24 Publication of JPS62270591A publication Critical patent/JPS62270591A/ja

1990-02-28 Publication of JPH029034B2 publication Critical patent/JPH029034B2/ja

Status Granted legal-status Critical Current

Links

ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 claims description 12
150000001875 compounds Chemical class 0.000 claims description 11
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims description 4
238000004519 manufacturing process Methods 0.000 claims description 3
239000002904 solvent Substances 0.000 claims description 3
125000001424 substituent group Chemical group 0.000 claims description 3
150000007530 organic bases Chemical class 0.000 claims description 2
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 claims description 2
125000005843 halogen group Chemical group 0.000 claims 1
150000003904 phospholipids Chemical class 0.000 description 7
239000000047 product Substances 0.000 description 7
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 6
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 6
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 5
238000010521 absorption reaction Methods 0.000 description 5
229920000642 polymer Polymers 0.000 description 5
IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 4
239000000243 solution Substances 0.000 description 4
WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
238000006243 chemical reaction Methods 0.000 description 3
238000000921 elemental analysis Methods 0.000 description 3
-1 polytetramethylene Polymers 0.000 description 3
YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 3
JNSGYXHNMZDPSI-MAZCIEHSSA-N CCCCC\C=C/C\C=C/CCCCCCCC(=O)OCC(CO)(CO)COC(=O)CCCCCCC\C=C/C\C=C/CCCCC Chemical compound CCCCC\C=C/C\C=C/CCCCCCCC(=O)OCC(CO)(CO)COC(=O)CCCCCCC\C=C/C\C=C/CCCCC JNSGYXHNMZDPSI-MAZCIEHSSA-N 0.000 description 2
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
102000004190 Enzymes Human genes 0.000 description 2
108090000790 Enzymes Proteins 0.000 description 2
IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 2
WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 2
230000007910 cell fusion Effects 0.000 description 2
239000012528 membrane Substances 0.000 description 2
239000000178 monomer Substances 0.000 description 2
210000000056 organ Anatomy 0.000 description 2
229920001223 polyethylene glycol Polymers 0.000 description 2
239000002244 precipitate Substances 0.000 description 2
YPFDHNVEDLHUCE-UHFFFAOYSA-N propane-1,3-diol Chemical compound OCCCO YPFDHNVEDLHUCE-UHFFFAOYSA-N 0.000 description 2
239000012265 solid product Substances 0.000 description 2
UWHCKJMYHZGTIT-UHFFFAOYSA-N tetraethylene glycol Chemical compound OCCOCCOCCOCCO UWHCKJMYHZGTIT-UHFFFAOYSA-N 0.000 description 2
GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical compound CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 description 2
SZCWBURCISJFEZ-UHFFFAOYSA-N (3-hydroxy-2,2-dimethylpropyl) 3-hydroxy-2,2-dimethylpropanoate Chemical compound OCC(C)(C)COC(=O)C(C)(C)CO SZCWBURCISJFEZ-UHFFFAOYSA-N 0.000 description 1
TZCPCKNHXULUIY-RGULYWFUSA-N 1,2-distearoyl-sn-glycero-3-phosphoserine Chemical compound CCCCCCCCCCCCCCCCCC(=O)OC[C@H](COP(O)(=O)OC[C@H](N)C(O)=O)OC(=O)CCCCCCCCCCCCCCCCC TZCPCKNHXULUIY-RGULYWFUSA-N 0.000 description 1
229940043375 1,5-pentanediol Drugs 0.000 description 1
IIZPXYDJLKNOIY-JXPKJXOSSA-N 1-palmitoyl-2-arachidonoyl-sn-glycero-3-phosphocholine Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCC\C=C/C\C=C/C\C=C/C\C=C/CCCCC IIZPXYDJLKNOIY-JXPKJXOSSA-N 0.000 description 1
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 1
JZNWSCPGTDBMEW-UHFFFAOYSA-N Glycerophosphorylethanolamin Natural products NCCOP(O)(=O)OCC(O)CO JZNWSCPGTDBMEW-UHFFFAOYSA-N 0.000 description 1
ZWZWYGMENQVNFU-UHFFFAOYSA-N Glycerophosphorylserin Natural products OC(=O)C(N)COP(O)(=O)OCC(O)CO ZWZWYGMENQVNFU-UHFFFAOYSA-N 0.000 description 1
QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 1
238000004566 IR spectroscopy Methods 0.000 description 1
ALQSHHUCVQOPAS-UHFFFAOYSA-N Pentane-1,5-diol Chemical compound OCCCCCO ALQSHHUCVQOPAS-UHFFFAOYSA-N 0.000 description 1
229920000562 Poly(ethylene adipate) Polymers 0.000 description 1
239000002202 Polyethylene glycol Substances 0.000 description 1
BJXXCOMGRRCAGN-XPWSMXQVSA-N [2,2-bis(hydroxymethyl)-3-[(e)-octadec-9-enoyl]oxypropyl] (e)-octadec-9-enoate Chemical compound CCCCCCCC\C=C\CCCCCCCC(=O)OCC(CO)(CO)COC(=O)CCCCCCC\C=C\CCCCCCCC BJXXCOMGRRCAGN-XPWSMXQVSA-N 0.000 description 1
WSETZJFXXOFEBR-UHFFFAOYSA-N [2,2-bis(hydroxymethyl)-3-tetradecanoyloxypropyl] tetradecanoate Chemical compound CCCCCCCCCCCCCC(=O)OCC(CO)(CO)COC(=O)CCCCCCCCCCCCC WSETZJFXXOFEBR-UHFFFAOYSA-N 0.000 description 1
QSLBMRULKKYEHX-UHFFFAOYSA-N [2-(hexadecanoyloxymethyl)-3-hydroxy-2-(hydroxymethyl)propyl] hexadecanoate Chemical compound CCCCCCCCCCCCCCCC(=O)OCC(CO)(CO)COC(=O)CCCCCCCCCCCCCCC QSLBMRULKKYEHX-UHFFFAOYSA-N 0.000 description 1
IETYWXORNPVXNT-UHFFFAOYSA-N [2-(hexanoyloxymethyl)-3-hydroxy-2-(hydroxymethyl)propyl] hexanoate Chemical compound CCCCCC(=O)OCC(CO)(CO)COC(=O)CCCCC IETYWXORNPVXNT-UHFFFAOYSA-N 0.000 description 1
WNLRTRBMVRJNCN-UHFFFAOYSA-L adipate(2-) Chemical compound [O-]C(=O)CCCCC([O-])=O WNLRTRBMVRJNCN-UHFFFAOYSA-L 0.000 description 1
238000004458 analytical method Methods 0.000 description 1
230000023555 blood coagulation Effects 0.000 description 1
210000005013 brain tissue Anatomy 0.000 description 1
210000000170 cell membrane Anatomy 0.000 description 1
239000007795 chemical reaction product Substances 0.000 description 1
210000000805 cytoplasm Anatomy 0.000 description 1
FOTKYAAJKYLFFN-UHFFFAOYSA-N decane-1,10-diol Chemical compound OCCCCCCCCCCO FOTKYAAJKYLFFN-UHFFFAOYSA-N 0.000 description 1
238000010586 diagram Methods 0.000 description 1
150000004985 diamines Chemical class 0.000 description 1
150000002009 diols Chemical class 0.000 description 1
230000000694 effects Effects 0.000 description 1
238000001914 filtration Methods 0.000 description 1
235000019256 formaldehyde Nutrition 0.000 description 1
230000006870 function Effects 0.000 description 1
SXCBDZAEHILGLM-UHFFFAOYSA-N heptane-1,7-diol Chemical compound OCCCCCCCO SXCBDZAEHILGLM-UHFFFAOYSA-N 0.000 description 1
XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 description 1
125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
239000000787 lecithin Substances 0.000 description 1
229940067606 lecithin Drugs 0.000 description 1
235000010445 lecithin Nutrition 0.000 description 1
239000007788 liquid Substances 0.000 description 1
239000000463 material Substances 0.000 description 1
230000004060 metabolic process Effects 0.000 description 1
238000000034 method Methods 0.000 description 1
239000011259 mixed solution Substances 0.000 description 1
229930014626 natural product Natural products 0.000 description 1
OEIJHBUUFURJLI-UHFFFAOYSA-N octane-1,8-diol Chemical compound OCCCCCCCCO OEIJHBUUFURJLI-UHFFFAOYSA-N 0.000 description 1
150000008104 phosphatidylethanolamines Chemical class 0.000 description 1
229920001451 polypropylene glycol Polymers 0.000 description 1
239000002994 raw material Substances 0.000 description 1
238000007151 ring opening polymerisation reaction Methods 0.000 description 1
230000014860 sensory perception of taste Effects 0.000 description 1
238000003756 stirring Methods 0.000 description 1

JP6578187A 1987-03-23 1987-03-23 （２−オキソ−１，３，２−ジオキサホスホリル）グリコキシ−２−オキソ−１，３，２−ジオキサホスホラン及びその製造方法 Granted JPS62270591A (ja)

Priority Applications (1)

Application Number	Priority Date	Filing Date	Title
JP6578187A JPS62270591A (ja)	1987-03-23	1987-03-23	（２−オキソ−１，３，２−ジオキサホスホリル）グリコキシ−２−オキソ−１，３，２−ジオキサホスホラン及びその製造方法

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
JP6578187A JPS62270591A (ja)	1987-03-23	1987-03-23	（２−オキソ−１，３，２−ジオキサホスホリル）グリコキシ−２−オキソ−１，３，２−ジオキサホスホラン及びその製造方法

Related Parent Applications (1)

Application Number	Title	Priority Date	Filing Date
JP58036649A Division JPS59164331A (ja)	1983-03-08	1983-03-08	リン脂質類似構造を有するポリマー並びにその製造方法

Publications (2)

Publication Number	Publication Date
JPS62270591A JPS62270591A (ja)	1987-11-24
JPH029034B2 true JPH029034B2 (de)	1990-02-28

Family

ID=13296922

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP6578187A Granted JPS62270591A (ja)	1987-03-23	1987-03-23	（２−オキソ−１，３，２−ジオキサホスホリル）グリコキシ−２−オキソ−１，３，２−ジオキサホスホラン及びその製造方法

Country Status (1)

Country	Link
JP (1)	JPS62270591A (de)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
WO2012175923A1 (en)	2011-06-24	2012-12-27	Biointeractions Limited, University Of Reading	Biocompatible, biomimetic ampholyte materials

1987
- 1987-03-23 JP JP6578187A patent/JPS62270591A/ja active Granted

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
WO2012175923A1 (en)	2011-06-24	2012-12-27	Biointeractions Limited, University Of Reading	Biocompatible, biomimetic ampholyte materials

Also Published As

Publication number	Publication date
JPS62270591A (ja)	1987-11-24

Publication	Publication Date	Title
Knani et al.	1993	Enzymatic polyesterification in organic media. Enzyme‐catalyzed synthesis of linear polyesters. I. Condensation polymerization of linear hydroxyesters. II. Ring‐opening polymerization of ϵ‐caprolactone
EP0275293B1 (de)	1992-10-21	Polyester
JP3241505B2 (ja)	2001-12-25	生分解性光学活性コポリマー及びその製造方法
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Y. Yuen et al.	2018	Biodegradable polycarbonate iongels for electrophysiology measurements
Rubio Hernández-Sampelayo et al.	2022	Biodegradable and biocompatible thermoplastic poly (ester-urethane) s based on poly (ε-caprolactone) and novel 1, 3-propanediol bis (4-isocyanatobenzoate) diisocyanate: synthesis and characterization
JPH029034B2 (de)	1990-02-28
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US6048523A (en)	2000-04-11	Polyester cyclic compounds, their complexes and bonded bodies
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JP2001288222A (ja)	2001-10-16	ベチュリンから得られるポリマー及びその製造法
JPH023415A (ja)	1990-01-09	新規アルファーオキシ酸ポリマー
JPS59164331A (ja)	1984-09-17	リン脂質類似構造を有するポリマー並びにその製造方法
JPH0316364B2 (de)	1991-03-05
JP4441032B2 (ja)	2010-03-31	二官能性有機リン化合物、重合体、及び用途
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AU2019230476B2 (en)	2024-11-14	Carbonate-linked surface modifying macromolecules
CN1159310C (zh)	2004-07-28	2-乙氧羰基-2-甲基三亚甲基碳酸酯及其制备方法
JPH08134085A (ja)	1996-05-28	リン脂質類似構造を有するポリウレタン化合物
JPH02238007A (ja)	1990-09-20	天然リン脂質類似構造を有する化合物及びポリマー並びにその製造方法
Elango et al.	2024	Investigation on Poly (2-Oxybutane-1-yl (4-Oxynapthalene-1-yl) Sebacoylate Random Block Copolyester

JPH029034B2 - - Google Patents

Info

Links

Priority Applications (1)

Applications Claiming Priority (1)

Related Parent Applications (1)

Publications (2)

Family

ID=13296922

Family Applications (1)

Country Status (1)

Cited By (1)

Cited By (1)

Also Published As

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