ES2538802T3 - Derivados de aminopiperinina 4-N-(disustituidos) como aditivos para masas de moldeo de poliamida y su uso - Google Patents
Derivados de aminopiperinina 4-N-(disustituidos) como aditivos para masas de moldeo de poliamida y su uso Download PDFInfo
- Publication number
- ES2538802T3 ES2538802T3 ES13152696.4T ES13152696T ES2538802T3 ES 2538802 T3 ES2538802 T3 ES 2538802T3 ES 13152696 T ES13152696 T ES 13152696T ES 2538802 T3 ES2538802 T3 ES 2538802T3
- Authority
- ES
- Spain
- Prior art keywords
- additive
- polyamide molding
- independently
- molding mass
- respectively independently
- 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.)
- Active
Links
- 239000000654 additive Substances 0.000 title claims abstract description 38
- 239000004952 Polyamide Substances 0.000 title claims description 19
- 229920002647 polyamide Polymers 0.000 title claims description 19
- 238000000465 moulding Methods 0.000 title claims description 12
- 230000000996 additive effect Effects 0.000 claims abstract description 31
- 125000004400 (C1-C12) alkyl group Chemical group 0.000 claims abstract description 5
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 5
- 125000003118 aryl group Chemical group 0.000 claims abstract description 3
- JBKVHLHDHHXQEQ-UHFFFAOYSA-N epsilon-caprolactam Chemical compound O=C1CCCCCN1 JBKVHLHDHHXQEQ-UHFFFAOYSA-N 0.000 claims description 22
- 229920000642 polymer Polymers 0.000 claims description 17
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 claims description 12
- 239000004753 textile Substances 0.000 claims description 7
- 238000002360 preparation method Methods 0.000 claims description 6
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 5
- 238000009833 condensation Methods 0.000 claims description 5
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 claims description 4
- 125000001931 aliphatic group Chemical group 0.000 claims description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 2
- 239000001361 adipic acid Substances 0.000 claims description 2
- 235000011037 adipic acid Nutrition 0.000 claims description 2
- 150000001735 carboxylic acids Chemical class 0.000 claims description 2
- 230000005494 condensation Effects 0.000 claims description 2
- 239000000203 mixture Substances 0.000 claims description 2
- 125000003158 alcohol group Chemical group 0.000 claims 1
- 125000003277 amino group Chemical group 0.000 claims 1
- 230000001588 bifunctional effect Effects 0.000 claims 1
- 125000002057 carboxymethyl group Chemical group [H]OC(=O)C([H])([H])[*] 0.000 claims 1
- 238000009987 spinning Methods 0.000 description 10
- 238000009826 distribution Methods 0.000 description 9
- 230000000052 comparative effect Effects 0.000 description 7
- 150000001875 compounds Chemical class 0.000 description 7
- 238000011084 recovery Methods 0.000 description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 239000000178 monomer Substances 0.000 description 5
- 238000010186 staining Methods 0.000 description 5
- 238000006068 polycondensation reaction Methods 0.000 description 4
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 230000008569 process Effects 0.000 description 3
- 230000006641 stabilisation Effects 0.000 description 3
- 238000011105 stabilization Methods 0.000 description 3
- 239000003381 stabilizer Substances 0.000 description 3
- FTVFPPFZRRKJIH-UHFFFAOYSA-N 2,2,6,6-tetramethylpiperidin-4-amine Chemical compound CC1(C)CC(N)CC(C)(C)N1 FTVFPPFZRRKJIH-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- 230000003078 antioxidant effect Effects 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 238000004043 dyeing Methods 0.000 description 2
- 230000002349 favourable effect Effects 0.000 description 2
- 230000000704 physical effect Effects 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 150000003512 tertiary amines Chemical class 0.000 description 2
- DRSHXJFUUPIBHX-UHFFFAOYSA-N COc1ccc(cc1)N1N=CC2C=NC(Nc3cc(OC)c(OC)c(OCCCN4CCN(C)CC4)c3)=NC12 Chemical compound COc1ccc(cc1)N1N=CC2C=NC(Nc3cc(OC)c(OC)c(OCCCN4CCN(C)CC4)c3)=NC12 DRSHXJFUUPIBHX-UHFFFAOYSA-N 0.000 description 1
- 229920002292 Nylon 6 Polymers 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- NLFBCYMMUAKCPC-KQQUZDAGSA-N ethyl (e)-3-[3-amino-2-cyano-1-[(e)-3-ethoxy-3-oxoprop-1-enyl]sulfanyl-3-oxoprop-1-enyl]sulfanylprop-2-enoate Chemical compound CCOC(=O)\C=C\SC(=C(C#N)C(N)=O)S\C=C\C(=O)OCC NLFBCYMMUAKCPC-KQQUZDAGSA-N 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 150000003053 piperidines Chemical class 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 239000000779 smoke Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
- 125000001302 tertiary amino group Chemical group 0.000 description 1
- 239000003017 thermal stabilizer Substances 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
- C08G69/02—Polyamides derived from amino-carboxylic acids or from polyamines and polycarboxylic acids
- C08G69/26—Polyamides derived from amino-carboxylic acids or from polyamines and polycarboxylic acids derived from polyamines and polycarboxylic acids
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
- C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D211/06—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
- C07D211/36—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D211/56—Nitrogen atoms
- C07D211/58—Nitrogen atoms attached in position 4
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Polyamides (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Hydrogenated Pyridines (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP13152696.4A EP2759534B1 (de) | 2013-01-25 | 2013-01-25 | 4-N-(disubstituierte)-Aminopiperininderivateals Additive für Polyamidformmassen und deren Verwendung |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES2538802T3 true ES2538802T3 (es) | 2015-06-24 |
Family
ID=47605400
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES13152696.4T Active ES2538802T3 (es) | 2013-01-25 | 2013-01-25 | Derivados de aminopiperinina 4-N-(disustituidos) como aditivos para masas de moldeo de poliamida y su uso |
Country Status (10)
| Country | Link |
|---|---|
| US (1) | US9908973B2 (enExample) |
| EP (1) | EP2759534B1 (enExample) |
| JP (1) | JP6496249B2 (enExample) |
| KR (1) | KR20150125645A (enExample) |
| CN (1) | CN105143184B (enExample) |
| EA (1) | EA029652B1 (enExample) |
| ES (1) | ES2538802T3 (enExample) |
| PL (1) | PL2759534T3 (enExample) |
| TW (1) | TWI602877B (enExample) |
| WO (1) | WO2014114721A1 (enExample) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| MX2022010952A (es) | 2020-03-05 | 2022-10-07 | C4 Therapeutics Inc | Compuestos para la degradacion dirigida de brd9. |
| CA3258672A1 (en) | 2022-06-16 | 2023-12-21 | Amphista Therapeutics Limited | BIFUNCTIONAL MOLECULES FOR TARGETED PROTEIN DEGRADATION |
| JP2025531881A (ja) | 2022-09-13 | 2025-09-25 | アンフィスタ セラピューティクス リミテッド | 標的タンパク質分解のための化合物 |
| GB202319256D0 (en) | 2023-12-15 | 2024-01-31 | Amphista Therapeutics Ltd | Novel compounds for targeted protein degradation |
| WO2025191109A1 (en) | 2024-03-13 | 2025-09-18 | Amphista Therapeutics Limited | Combinations comprising brd9 bifunctional compounds and their use in the treatment of cancer |
Family Cites Families (23)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4191683A (en) * | 1975-05-28 | 1980-03-04 | Ciba-Geigy Corporation | Derivatives of 4-aminopiperidine as stabilizers for polymers |
| DE2545647C3 (de) * | 1975-10-11 | 1982-03-11 | Bayer Ag, 5090 Leverkusen | Stabilisierung synthetischer Polymerer |
| CH623066A5 (enExample) * | 1976-05-11 | 1981-05-15 | Ciba Geigy Ag | |
| DE2642386A1 (de) | 1976-09-21 | 1978-03-23 | Bayer Ag | Permanent stabilisierte polyurethane |
| DE2642374A1 (de) * | 1976-09-21 | 1978-03-23 | Bayer Ag | Permanent stabilisierte polyurethane |
| US4348524A (en) * | 1980-03-28 | 1982-09-07 | Ciba-Geigy Corporation | Amide derivatives of polyalkylpiperidines |
| AU7424681A (en) * | 1980-09-10 | 1982-03-18 | B.F. Goodrich Company, The | Piperidine derivatives as u.v. stabilisers |
| CA1266272A (en) * | 1983-05-27 | 1990-02-27 | Masakatsu Yoshimura | A 2,2,6,6-tetramethylpiperidine derivative, its production and a stabilizer for synthetic resins containing the same |
| JPS59219346A (ja) | 1983-05-27 | 1984-12-10 | Sumitomo Chem Co Ltd | 合成樹脂用安定剤 |
| DE3328134C2 (de) * | 1983-08-04 | 1986-08-07 | Hüls AG, 4370 Marl | EP-Pulverlacke und Verfahren zur Herstellung matter Überzüge |
| US5112979A (en) | 1990-11-29 | 1992-05-12 | Texaco Chemical Company | Polyoxyalkyleneamines containing tetraalkylpiperidine functionality and their use as light, heat and oxidation stabilizers |
| KR100232977B1 (ko) | 1994-04-15 | 1999-12-01 | 스타르크 카르크 | 본질적으로 광 및 열에 안정한 폴리아미드 |
| US5618909A (en) * | 1995-07-27 | 1997-04-08 | Alliedsignal Inc. | Light stabilized polyamide substrate and process for making |
| DE19645166A1 (de) | 1996-11-02 | 1998-05-07 | Huels Chemische Werke Ag | Blockierte Polyisocyanate mit eingebautem HALS-Stabilisator |
| MY127653A (en) * | 1996-05-16 | 2006-12-29 | Toray Industries | Biaxially stretched polyester film for forming container and method of producing the film |
| RU2156264C2 (ru) | 1996-07-09 | 2000-09-20 | Емс-Инвента АГ | Устойчивый к атмосферным воздействиям полиамид и способ его получения (варианты) |
| DE19804980A1 (de) * | 1998-02-07 | 1999-08-12 | Huels Chemische Werke Ag | Hydroxyl- und uretdiongruppenhaltige Polyisocyanate mit eingebautem HALS-Stabilisator, ein Verfahren zu ihrer Herstellung und deren Verwendung |
| DE19812135A1 (de) * | 1998-03-20 | 1999-09-23 | Basf Ag | Inhärent licht- und hitzestabilisierte Polyamide mit verbesserter Naßechtheit |
| DE19854421B4 (de) | 1998-11-25 | 2006-11-02 | Ems-Inventa Ag | Verfahren zur Herstellung von Polyamid-6 für Spinnzwecke |
| US6620438B2 (en) * | 2001-03-08 | 2003-09-16 | Boehringer Ingelheim Pharma Kg | Pharmaceutical compositions based on anticholinergics and NK1-receptor antagonists |
| US7998886B2 (en) * | 2005-10-24 | 2011-08-16 | Milliken & Company | Hindered amine treated textiles |
| DE102008026075B4 (de) | 2008-05-30 | 2015-04-30 | Lurgi Zimmer Gmbh | Verfahren zur Herstellung von Polyamiden unter Verwendung von Carbonsäuren und Amiden |
| DE102008002607A1 (de) | 2008-06-24 | 2009-12-31 | Robert Bosch Gmbh | Schweißvorrichtung |
-
2013
- 2013-01-25 EP EP13152696.4A patent/EP2759534B1/de not_active Not-in-force
- 2013-01-25 ES ES13152696.4T patent/ES2538802T3/es active Active
- 2013-01-25 PL PL13152696T patent/PL2759534T3/pl unknown
-
2014
- 2014-01-22 TW TW103102197A patent/TWI602877B/zh not_active IP Right Cessation
- 2014-01-23 JP JP2015554146A patent/JP6496249B2/ja not_active Expired - Fee Related
- 2014-01-23 CN CN201480006196.3A patent/CN105143184B/zh not_active Expired - Fee Related
- 2014-01-23 KR KR1020157019718A patent/KR20150125645A/ko not_active Abandoned
- 2014-01-23 WO PCT/EP2014/051343 patent/WO2014114721A1/de not_active Ceased
- 2014-01-23 EA EA201591060A patent/EA029652B1/ru not_active IP Right Cessation
- 2014-01-23 US US14/763,086 patent/US9908973B2/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| WO2014114721A1 (de) | 2014-07-31 |
| JP2016511777A (ja) | 2016-04-21 |
| US9908973B2 (en) | 2018-03-06 |
| TWI602877B (zh) | 2017-10-21 |
| KR20150125645A (ko) | 2015-11-09 |
| CN105143184B (zh) | 2017-10-03 |
| EP2759534B1 (de) | 2015-03-11 |
| CN105143184A (zh) | 2015-12-09 |
| EA029652B1 (ru) | 2018-04-30 |
| US20150329671A1 (en) | 2015-11-19 |
| EP2759534A1 (de) | 2014-07-30 |
| PL2759534T3 (pl) | 2015-08-31 |
| TW201439206A (zh) | 2014-10-16 |
| JP6496249B2 (ja) | 2019-04-03 |
| EA201591060A1 (ru) | 2015-12-30 |
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