CA2060269C - Polyether bloc amides, leur procede de synthese - Google Patents
Polyether bloc amides, leur procede de syntheseInfo
- Publication number
- CA2060269C CA2060269C CA002060269A CA2060269A CA2060269C CA 2060269 C CA2060269 C CA 2060269C CA 002060269 A CA002060269 A CA 002060269A CA 2060269 A CA2060269 A CA 2060269A CA 2060269 C CA2060269 C CA 2060269C
- Authority
- CA
- Canada
- Prior art keywords
- diacid
- polyether block
- block amides
- polyether
- oligoamide
- 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 - Fee Related
Links
- 238000000034 method Methods 0.000 title claims description 13
- 239000004721 Polyphenylene oxide Substances 0.000 title description 8
- 229920000570 polyether Polymers 0.000 title description 8
- 239000004952 Polyamide Substances 0.000 title description 5
- 229920002647 polyamide Polymers 0.000 title description 5
- 230000002194 synthesizing effect Effects 0.000 title 1
- 229920002614 Polyether block amide Polymers 0.000 claims description 27
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 14
- NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 claims description 12
- 150000004985 diamines Chemical class 0.000 claims description 10
- 238000006068 polycondensation reaction Methods 0.000 claims description 10
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 claims description 9
- 239000003054 catalyst Substances 0.000 claims description 8
- 229920000642 polymer Polymers 0.000 claims description 8
- JHWNWJKBPDFINM-UHFFFAOYSA-N Laurolactam Chemical compound O=C1CCCCCCCCCCCN1 JHWNWJKBPDFINM-UHFFFAOYSA-N 0.000 claims description 7
- 230000015572 biosynthetic process Effects 0.000 claims description 7
- QFTYSVGGYOXFRQ-UHFFFAOYSA-N dodecane-1,12-diamine Chemical compound NCCCCCCCCCCCCN QFTYSVGGYOXFRQ-UHFFFAOYSA-N 0.000 claims description 7
- 238000003786 synthesis reaction Methods 0.000 claims description 7
- JBKVHLHDHHXQEQ-UHFFFAOYSA-N epsilon-caprolactam Chemical compound O=C1CCCCCN1 JBKVHLHDHHXQEQ-UHFFFAOYSA-N 0.000 claims description 6
- 238000006116 polymerization reaction Methods 0.000 claims description 5
- 125000004432 carbon atom Chemical group C* 0.000 claims description 4
- PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 claims description 3
- 125000003118 aryl group Chemical group 0.000 claims description 3
- 229920001400 block copolymer Polymers 0.000 claims description 3
- 239000000178 monomer Substances 0.000 claims description 3
- 229920005604 random copolymer Polymers 0.000 claims description 3
- 150000003839 salts Chemical class 0.000 claims description 3
- DZIHTWJGPDVSGE-UHFFFAOYSA-N 4-[(4-aminocyclohexyl)methyl]cyclohexan-1-amine Chemical compound C1CC(N)CCC1CC1CCC(N)CC1 DZIHTWJGPDVSGE-UHFFFAOYSA-N 0.000 claims description 2
- FDLQZKYLHJJBHD-UHFFFAOYSA-N [3-(aminomethyl)phenyl]methanamine Chemical compound NCC1=CC=CC(CN)=C1 FDLQZKYLHJJBHD-UHFFFAOYSA-N 0.000 claims description 2
- 150000001413 amino acids Chemical class 0.000 claims description 2
- 239000002131 composite material Substances 0.000 claims description 2
- 150000003951 lactams Chemical class 0.000 claims description 2
- BJZYYSAMLOBSDY-QMMMGPOBSA-N (2s)-2-butoxybutan-1-ol Chemical compound CCCCO[C@@H](CC)CO BJZYYSAMLOBSDY-QMMMGPOBSA-N 0.000 claims 2
- 125000001931 aliphatic group Chemical group 0.000 claims 2
- 125000001183 hydrocarbyl group Chemical group 0.000 claims 2
- 238000006243 chemical reaction Methods 0.000 abstract description 19
- 229920001577 copolymer Polymers 0.000 abstract 1
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 54
- 229910052757 nitrogen Inorganic materials 0.000 description 27
- 238000002844 melting Methods 0.000 description 19
- 230000008018 melting Effects 0.000 description 19
- 239000000203 mixture Substances 0.000 description 9
- 229920002725 thermoplastic elastomer Polymers 0.000 description 9
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 8
- 239000002253 acid Substances 0.000 description 8
- 238000003756 stirring Methods 0.000 description 8
- 150000002009 diols Chemical class 0.000 description 6
- TVIDDXQYHWJXFK-UHFFFAOYSA-N dodecanedioic acid Chemical compound OC(=O)CCCCCCCCCCC(O)=O TVIDDXQYHWJXFK-UHFFFAOYSA-N 0.000 description 6
- 239000012429 reaction media Substances 0.000 description 6
- 229910001220 stainless steel Inorganic materials 0.000 description 6
- 239000010935 stainless steel Substances 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 239000000243 solution Substances 0.000 description 5
- 239000004698 Polyethylene Substances 0.000 description 4
- 239000002202 Polyethylene glycol Substances 0.000 description 4
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 4
- 150000001408 amides Chemical class 0.000 description 4
- 239000007864 aqueous solution Substances 0.000 description 4
- SNRUBQQJIBEYMU-UHFFFAOYSA-N dodecane Chemical compound CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 4
- 238000010438 heat treatment Methods 0.000 description 4
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 4
- RLSSMJSEOOYNOY-UHFFFAOYSA-N m-cresol Chemical compound CC1=CC=CC(O)=C1 RLSSMJSEOOYNOY-UHFFFAOYSA-N 0.000 description 4
- 229920001223 polyethylene glycol Polymers 0.000 description 4
- 238000010926 purge Methods 0.000 description 4
- 239000011541 reaction mixture Substances 0.000 description 4
- 238000013019 agitation Methods 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 229920001971 elastomer Polymers 0.000 description 3
- 239000000806 elastomer Substances 0.000 description 3
- 230000032050 esterification Effects 0.000 description 3
- 238000005886 esterification reaction Methods 0.000 description 3
- 239000011521 glass Substances 0.000 description 3
- -1 hydrocarbon radical Chemical class 0.000 description 3
- 229920001169 thermoplastic Polymers 0.000 description 3
- 239000004416 thermosoftening plastic Substances 0.000 description 3
- 239000004215 Carbon black (E152) Substances 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 2
- 239000003153 chemical reaction reagent Substances 0.000 description 2
- 230000004927 fusion Effects 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 238000000265 homogenisation Methods 0.000 description 2
- 229930195733 hydrocarbon Natural products 0.000 description 2
- 229920003023 plastic Polymers 0.000 description 2
- 239000004033 plastic Substances 0.000 description 2
- 229920001451 polypropylene glycol Polymers 0.000 description 2
- 229920001187 thermosetting polymer Polymers 0.000 description 2
- QFGCFKJIPBRJGM-UHFFFAOYSA-N 12-[(2-methylpropan-2-yl)oxy]-12-oxododecanoic acid Chemical compound CC(C)(C)OC(=O)CCCCCCCCCCC(O)=O QFGCFKJIPBRJGM-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 241000790917 Dioxys <bee> Species 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- 229910003953 H3PO2 Inorganic materials 0.000 description 1
- 244000062793 Sorghum vulgare Species 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical group [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical group [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 description 1
- ZOIORXHNWRGPMV-UHFFFAOYSA-N acetic acid;zinc Chemical compound [Zn].CC(O)=O.CC(O)=O ZOIORXHNWRGPMV-UHFFFAOYSA-N 0.000 description 1
- 229920000122 acrylonitrile butadiene styrene Polymers 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 150000001279 adipic acids Chemical class 0.000 description 1
- 230000009435 amidation Effects 0.000 description 1
- 238000007112 amidation reaction Methods 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- FOTKYAAJKYLFFN-UHFFFAOYSA-N decane-1,10-diol Chemical compound OCCCCCCCCCCO FOTKYAAJKYLFFN-UHFFFAOYSA-N 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 238000000280 densification Methods 0.000 description 1
- 150000001991 dicarboxylic acids Chemical class 0.000 description 1
- 238000011010 flushing procedure Methods 0.000 description 1
- 229910052735 hafnium Inorganic materials 0.000 description 1
- VBJZVLUMGGDVMO-UHFFFAOYSA-N hafnium atom Chemical group [Hf] VBJZVLUMGGDVMO-UHFFFAOYSA-N 0.000 description 1
- 125000004836 hexamethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[*:1] 0.000 description 1
- 150000002430 hydrocarbons Chemical group 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 235000019713 millet Nutrition 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- ACVYVLVWPXVTIT-UHFFFAOYSA-N phosphinic acid Chemical compound O[PH2]=O ACVYVLVWPXVTIT-UHFFFAOYSA-N 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920001955 polyphenylene ether Polymers 0.000 description 1
- 229920000909 polytetrahydrofuran Polymers 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 150000003504 terephthalic acids Chemical class 0.000 description 1
- ISIJQEHRDSCQIU-UHFFFAOYSA-N tert-butyl 2,7-diazaspiro[4.5]decane-7-carboxylate Chemical compound C1N(C(=O)OC(C)(C)C)CCCC11CNCC1 ISIJQEHRDSCQIU-UHFFFAOYSA-N 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 230000009466 transformation Effects 0.000 description 1
- 239000004246 zinc acetate Substances 0.000 description 1
- 229910052726 zirconium Chemical group 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G69/00—Macromolecular compounds obtained by reactions forming a carboxylic amide link in the main chain of the macromolecule
- C08G69/44—Polyester-amides
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G69/00—Macromolecular compounds obtained by reactions forming a carboxylic amide link in the main chain of the macromolecule
- C08G69/40—Polyamides containing oxygen in the form of ether groups
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G69/00—Macromolecular compounds obtained by reactions forming a carboxylic amide link in the main chain of the macromolecule
- C08G69/48—Polymers modified by chemical after-treatment
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
- Y10T428/2913—Rod, strand, filament or fiber
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
- Y10T428/2913—Rod, strand, filament or fiber
- Y10T428/2929—Bicomponent, conjugate, composite or collateral fibers or filaments [i.e., coextruded sheath-core or side-by-side type]
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
- Y10T428/2913—Rod, strand, filament or fiber
- Y10T428/2933—Coated or with bond, impregnation or core
- Y10T428/2964—Artificial fiber or filament
- Y10T428/2967—Synthetic resin or polymer
- Y10T428/2969—Polyamide, polyimide or polyester
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Polyamides (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Glass Compositions (AREA)
- Food-Manufacturing Devices (AREA)
- Medicines Containing Plant Substances (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Enzymes And Modification Thereof (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR9101032 | 1991-01-30 | ||
| FR9101032A FR2672053B1 (fr) | 1991-01-30 | 1991-01-30 | Polyether bloc amides, leur procede de synthese. |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CA2060269A1 CA2060269A1 (fr) | 1992-07-31 |
| CA2060269C true CA2060269C (fr) | 1996-09-24 |
Family
ID=9409194
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA002060269A Expired - Fee Related CA2060269C (fr) | 1991-01-30 | 1992-01-29 | Polyether bloc amides, leur procede de synthese |
Country Status (13)
| Country | Link |
|---|---|
| US (1) | US5213891A (enExample) |
| EP (1) | EP0506495B1 (enExample) |
| JP (1) | JP2635259B2 (enExample) |
| KR (1) | KR960007340B1 (enExample) |
| CN (1) | CN1036525C (enExample) |
| AT (1) | ATE146201T1 (enExample) |
| AU (1) | AU651168B2 (enExample) |
| CA (1) | CA2060269C (enExample) |
| DE (1) | DE69215732T2 (enExample) |
| FI (1) | FI920401L (enExample) |
| FR (1) | FR2672053B1 (enExample) |
| IE (1) | IE920300A1 (enExample) |
| NO (1) | NO920382L (enExample) |
Families Citing this family (52)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NZ239723A (en) * | 1990-09-18 | 1993-06-25 | Chicopee | Blends comprising a hydrophilic block poly (ether-co-amide) and a hydrophobic polymer |
| US5489667A (en) * | 1991-03-20 | 1996-02-06 | Atochem Deutschland Gmbh | Polyetheresteramides and process for making and using the same |
| DE69406686T2 (de) * | 1993-01-08 | 1998-05-20 | Tosoh Corp | Esteramid-Copolymere und ihre Herstellung |
| US5342918A (en) * | 1993-04-30 | 1994-08-30 | Texaco Chemical Company | Carboxyl-terminated polyetheramines |
| WO1996025451A1 (en) * | 1995-02-17 | 1996-08-22 | W.R. Grace & Co.-Conn. | Thermoplastic block copolymer with inherent anti-fog properties |
| DE69631449T2 (de) * | 1995-04-11 | 2004-09-16 | Atofina | Verpackung aus Polymeren mit Polyamid- und Polyetherblöcken zum Frischhalten von Produkten |
| US5845652A (en) * | 1995-06-06 | 1998-12-08 | Tseng; Mingchih M. | Dental floss |
| AU708978B2 (en) * | 1995-06-06 | 1999-08-19 | Gillette Canada Inc. | Dental floss |
| US6027592A (en) * | 1995-06-06 | 2000-02-22 | Gillette Canada Inc. | Dental floss |
| US5900471A (en) * | 1997-04-03 | 1999-05-04 | Alliedsignal Inc. | Films of blended nylon resins and laminates therefrom |
| AUPP610798A0 (en) | 1998-09-23 | 1998-10-15 | Swig Pty Ltd | Improved polymers |
| MXPA03000310A (es) * | 2000-07-12 | 2004-12-13 | Gryphon Therapeutics Inc | Quimiocinas sinteticas bioactivas, modificadas con polimeros y metodos para su elaboracion y uso. |
| KR20030057529A (ko) * | 2000-09-08 | 2003-07-04 | 그리폰 테라퓨틱스, 인코포레이티드 | 합성 적혈구생성 자극 단백질 |
| US7118737B2 (en) | 2000-09-08 | 2006-10-10 | Amylin Pharmaceuticals, Inc. | Polymer-modified synthetic proteins |
| US20040077835A1 (en) * | 2001-07-12 | 2004-04-22 | Robin Offord | Chemokine receptor modulators, production and use |
| EP1616003A4 (en) | 2002-12-30 | 2007-06-20 | Gryphon Therapeutics Inc | WATER-SOLUBLE THIOESTER AND SELENOESTER COMPOUNDS AND METHOD FOR THE PRODUCTION AND USE THEREOF |
| US8394471B2 (en) * | 2004-12-14 | 2013-03-12 | Parker-Hannifin Corporation | Electrically-conductive hose |
| EP1868652A2 (en) | 2005-04-05 | 2007-12-26 | Istituto di Richerche di Biologia Molecolare P. Angeletti S.p.A. | Method for shielding functional sites or epitopes on proteins |
| US7985783B2 (en) | 2006-09-21 | 2011-07-26 | The Regents Of The University Of California | Aldehyde tags, uses thereof in site-specific protein modification |
| FR2927631B1 (fr) | 2008-02-15 | 2010-03-05 | Arkema France | Utilisation d'un promoteur d'adherence dans une solution de nettoyage de la surface d'un substrat a base de tpe et/ou de pa, pour augmenter l'adherence dudit substrat avec les joints de colle aqueux. |
| FR2936803B1 (fr) | 2008-10-06 | 2012-09-28 | Arkema France | Copolymere a blocs issu de matieres renouvelables et procede de fabrication d'un tel copolymere a blocs. |
| FR2941700B1 (fr) | 2009-02-02 | 2012-03-16 | Arkema France | Procede de synthese d'un alliage de copolymere a blocs presentant des proprietes antistatiques ameliorees. |
| FR2954151B1 (fr) | 2009-12-17 | 2012-03-16 | Oreal | Utilisation d'une composition cosmetique comprenant au moins un polymere elastomere filmogene pour le traitement de la transpiration humaine |
| FR2958649B1 (fr) | 2010-04-07 | 2012-05-04 | Arkema France | Copolymere a blocs issu de matieres renouvelables et procede de fabrication d'un tel copolymere a blocs |
| JP5867387B2 (ja) * | 2010-05-19 | 2016-02-24 | 三菱瓦斯化学株式会社 | ポリエステルアミド化合物 |
| FR2960773B1 (fr) | 2010-06-03 | 2015-12-11 | Oreal | Procedes de traitement cosmetique utilisant un revetement a base d'un polymere polyamide-polyether |
| FR2972351B1 (fr) | 2011-03-09 | 2013-04-12 | Oreal | Procede de traitement cosmetique de la transpiration humaine comprenant l'application d'un film polymerique anti-transpirant solubilisable |
| CN103747807B (zh) | 2011-07-05 | 2016-12-07 | 比奥阿赛斯技术有限公司 | P97‑抗体缀合物和使用方法 |
| CA3140358A1 (en) | 2012-07-31 | 2014-02-06 | Bioasis Technologies, Inc. | Dephosphorylated lysosomal storage disease proteins and methods of use thereof |
| AU2013341711A1 (en) | 2012-11-12 | 2015-05-21 | Redwood Bioscience, Inc. | Compounds and methods for producing a conjugate |
| WO2014078733A1 (en) | 2012-11-16 | 2014-05-22 | The Regents Of The University Of California | Pictet-spengler ligation for protein chemical modification |
| US9310374B2 (en) | 2012-11-16 | 2016-04-12 | Redwood Bioscience, Inc. | Hydrazinyl-indole compounds and methods for producing a conjugate |
| AU2014243816B2 (en) | 2013-03-13 | 2019-01-31 | Bioasis Technologies Inc. | Fragments of p97 and uses thereof |
| US20150093399A1 (en) | 2013-08-28 | 2015-04-02 | Bioasis Technologies, Inc. | Cns-targeted conjugates having modified fc regions and methods of use thereof |
| FR3011550B1 (fr) * | 2013-10-07 | 2016-11-18 | Arkema France | Copolymere a blocs polyamide et a bloc polyether |
| CN115504924A (zh) | 2013-11-27 | 2022-12-23 | 雷德伍德生物科技股份有限公司 | 肼基-吡咯并化合物及用于生成缀合物的方法 |
| JP6897903B2 (ja) * | 2014-09-24 | 2021-07-07 | 株式会社ブリヂストン | タイヤ |
| EP3373937B1 (en) | 2015-11-09 | 2021-12-22 | R.P. Scherer Technologies, LLC | Anti-cd22 antibody-maytansine conjugates and methods of use thereof |
| AU2017250778B2 (en) | 2016-04-15 | 2021-09-23 | Beckman Coulter, Inc. | Photoactive macromolecules and uses thereof |
| JP7097885B2 (ja) | 2016-12-12 | 2022-07-08 | ベクトン・ディキンソン・アンド・カンパニー | 水溶性ポリマー色素 |
| CN119286279A (zh) | 2017-12-26 | 2025-01-10 | 贝克顿·迪金森公司 | 深紫外线可激发的水溶剂化聚合物染料 |
| EP3775052B1 (en) | 2018-03-30 | 2024-06-05 | Becton, Dickinson and Company | Water-soluble polymeric dyes having pendant chromophores |
| EP3813867A1 (en) | 2018-07-22 | 2021-05-05 | Bioasis Technologies Inc. | Treatment of lymmphatic metastases |
| FR3096683B1 (fr) | 2019-05-27 | 2022-03-04 | Arkema France | copolyesteramide auto-ignifugé |
| FR3096684B1 (fr) | 2019-05-29 | 2022-03-04 | Arkema France | Copolymère à blocs à résistance améliorée au sébum |
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| CN121866309A (zh) | 2023-09-21 | 2026-04-14 | 贝克曼库尔特有限公司 | 用于流式细胞术的二氢菲（dhp）桥接染料 |
Family Cites Families (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2273021B1 (enExample) * | 1974-05-31 | 1977-03-11 | Ato Chimie | |
| FR2378058A1 (fr) * | 1977-01-24 | 1978-08-18 | Ato Chimie | Copolyetheresteramides stables a l'hydrolyse |
| FR2401947A1 (fr) * | 1977-09-02 | 1979-03-30 | Ato Chimie | Procede de preparation de polyether-ester-amides sequences utilisables, entre autres, comme produits a mouler, a extruder ou a filer |
| DE2913460A1 (de) * | 1979-04-04 | 1980-10-16 | Bayer Ag | Estermodifizierte polyamide |
| DE2932234C2 (de) * | 1979-08-09 | 1982-01-28 | Chemische Werke Hüls AG, 4370 Marl | Verfahren zur Herstellung von Polyether(ester)amiden |
| DE2936976C2 (de) * | 1979-09-13 | 1986-09-18 | Hüls AG, 4370 Marl | Verfahren zur Herstellung von Polyether(ester)amiden |
| DE2936977C2 (de) * | 1979-09-13 | 1986-06-12 | Hüls AG, 4370 Marl | Verfahren zur Herstellung von Polyether(ester)amiden |
| FR2470141B1 (fr) * | 1979-11-19 | 1985-05-31 | Ato Chimie | Nouveau procede de synthese de copolycondensats sequences polyetheresteramide |
| JPS5790017A (en) * | 1980-11-25 | 1982-06-04 | Toray Ind Inc | Production of polyether-ester-amide |
| US4578451A (en) * | 1983-07-15 | 1986-03-25 | Ethicon, Inc. | Surgical filaments from block copolyetheramides |
| US4536563A (en) * | 1983-11-18 | 1985-08-20 | Daicel Chemical Industries, Ltd. | Process for manufacturing polyetheresteramide |
| JPS6335622A (ja) * | 1986-07-31 | 1988-02-16 | Asahi Chem Ind Co Ltd | ポリアミド弾性体の製造方法 |
| JPS6348332A (ja) * | 1986-08-15 | 1988-03-01 | Asahi Chem Ind Co Ltd | ポリエ−テルエステルアミドの製造方法 |
| JPS63182343A (ja) * | 1987-01-23 | 1988-07-27 | Asahi Chem Ind Co Ltd | ポリエ−テルエステルアミドの製造法 |
| JPS63277239A (ja) * | 1987-05-08 | 1988-11-15 | Asahi Chem Ind Co Ltd | ポリアミドエラストマ−の製造方法 |
-
1991
- 1991-01-30 FR FR9101032A patent/FR2672053B1/fr not_active Expired - Fee Related
-
1992
- 1992-01-27 EP EP92400205A patent/EP0506495B1/fr not_active Expired - Lifetime
- 1992-01-27 DE DE69215732T patent/DE69215732T2/de not_active Expired - Fee Related
- 1992-01-27 AT AT92400205T patent/ATE146201T1/de not_active IP Right Cessation
- 1992-01-29 KR KR1019920001291A patent/KR960007340B1/ko not_active Expired - Fee Related
- 1992-01-29 NO NO92920382A patent/NO920382L/no unknown
- 1992-01-29 FI FI920401A patent/FI920401L/fi not_active Application Discontinuation
- 1992-01-29 AU AU10560/92A patent/AU651168B2/en not_active Ceased
- 1992-01-29 CA CA002060269A patent/CA2060269C/fr not_active Expired - Fee Related
- 1992-01-29 IE IE030092A patent/IE920300A1/en unknown
- 1992-01-30 JP JP4015478A patent/JP2635259B2/ja not_active Expired - Fee Related
- 1992-01-30 CN CN92100711A patent/CN1036525C/zh not_active Expired - Fee Related
- 1992-01-30 US US07/828,150 patent/US5213891A/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| JPH04337325A (ja) | 1992-11-25 |
| FI920401A7 (fi) | 1992-07-31 |
| IE920300A1 (en) | 1992-07-29 |
| AU1056092A (en) | 1992-08-06 |
| DE69215732D1 (de) | 1997-01-23 |
| CA2060269A1 (fr) | 1992-07-31 |
| NO920382D0 (no) | 1992-01-29 |
| NO920382L (no) | 1992-07-31 |
| AU651168B2 (en) | 1994-07-14 |
| KR960007340B1 (ko) | 1996-05-31 |
| CN1063876A (zh) | 1992-08-26 |
| FI920401L (fi) | 1992-07-31 |
| KR920014859A (ko) | 1992-08-25 |
| US5213891A (en) | 1993-05-25 |
| FR2672053A1 (fr) | 1992-07-31 |
| EP0506495A2 (fr) | 1992-09-30 |
| EP0506495A3 (enExample) | 1994-03-02 |
| FI920401A0 (fi) | 1992-01-29 |
| FR2672053B1 (fr) | 1993-04-23 |
| ATE146201T1 (de) | 1996-12-15 |
| CN1036525C (zh) | 1997-11-26 |
| EP0506495B1 (fr) | 1996-12-11 |
| DE69215732T2 (de) | 1997-06-26 |
| JP2635259B2 (ja) | 1997-07-30 |
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Legal Events
| Date | Code | Title | Description |
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| EEER | Examination request | ||
| MKLA | Lapsed |