JP2005504868A5 - - Google Patents
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- Publication number
- JP2005504868A5 JP2005504868A5 JP2003534486A JP2003534486A JP2005504868A5 JP 2005504868 A5 JP2005504868 A5 JP 2005504868A5 JP 2003534486 A JP2003534486 A JP 2003534486A JP 2003534486 A JP2003534486 A JP 2003534486A JP 2005504868 A5 JP2005504868 A5 JP 2005504868A5
- Authority
- JP
- Japan
- Prior art keywords
- group
- carbon atoms
- alkyl
- substituted
- unsubstituted
- 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.)
- Ceased
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- 125000004432 carbon atom Chemical group C* 0.000 claims 125
- 125000000217 alkyl group Chemical group 0.000 claims 45
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 18
- 125000004430 oxygen atom Chemical group O* 0.000 claims 17
- 229910052717 sulfur Inorganic materials 0.000 claims 17
- 125000004434 sulfur atom Chemical group 0.000 claims 17
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 14
- 150000001875 compounds Chemical class 0.000 claims 13
- -1 5,6,7,8-tetrahydro-2-naphthyl group Chemical group 0.000 claims 11
- 229910052799 carbon Inorganic materials 0.000 claims 10
- 230000000087 stabilizing effect Effects 0.000 claims 10
- 125000003884 phenylalkyl group Chemical group 0.000 claims 9
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 8
- 125000004429 atom Chemical group 0.000 claims 7
- 125000002947 alkylene group Chemical group 0.000 claims 6
- 150000001721 carbon Chemical class 0.000 claims 6
- 125000000753 cycloalkyl group Chemical group 0.000 claims 6
- 239000004952 Polyamide Substances 0.000 claims 5
- 125000002252 acyl group Chemical group 0.000 claims 5
- 125000004423 acyloxy group Chemical group 0.000 claims 5
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 claims 5
- 125000001231 benzoyloxy group Chemical group C(C1=CC=CC=C1)(=O)O* 0.000 claims 5
- 230000015572 biosynthetic process Effects 0.000 claims 5
- 239000000356 contaminant Substances 0.000 claims 5
- 125000002485 formyl group Chemical class [H]C(*)=O 0.000 claims 5
- 238000010128 melt processing Methods 0.000 claims 5
- 229920002647 polyamide Polymers 0.000 claims 5
- 229920006149 polyester-amide block copolymer Polymers 0.000 claims 5
- 125000003545 alkoxy group Chemical group 0.000 claims 4
- 125000004457 alkyl amino carbonyl group Chemical group 0.000 claims 4
- 229920001577 copolymer Polymers 0.000 claims 4
- 125000001153 fluoro group Chemical group F* 0.000 claims 4
- 239000003381 stabilizer Substances 0.000 claims 4
- 125000005236 alkanoylamino group Chemical group 0.000 claims 3
- 125000004414 alkyl thio group Chemical group 0.000 claims 3
- 125000003277 amino group Chemical group 0.000 claims 3
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims 3
- 125000006254 cycloalkyl carbonyl group Chemical group 0.000 claims 3
- 125000002993 cycloalkylene group Chemical group 0.000 claims 3
- 229910052731 fluorine Inorganic materials 0.000 claims 3
- 229910052760 oxygen Inorganic materials 0.000 claims 3
- 239000001301 oxygen Substances 0.000 claims 3
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 claims 3
- 229920000642 polymer Polymers 0.000 claims 3
- 150000005846 sugar alcohols Polymers 0.000 claims 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims 2
- 125000003282 alkyl amino group Chemical group 0.000 claims 2
- 125000001118 alkylidene group Chemical group 0.000 claims 2
- 125000003710 aryl alkyl group Chemical group 0.000 claims 2
- 150000002430 hydrocarbons Chemical group 0.000 claims 2
- 125000004957 naphthylene group Chemical group 0.000 claims 2
- 125000005346 substituted cycloalkyl group Chemical group 0.000 claims 2
- 239000011593 sulfur Substances 0.000 claims 2
- 125000001544 thienyl group Chemical group 0.000 claims 2
- YJTKZCDBKVTVBY-UHFFFAOYSA-N 1,3-Diphenylbenzene Chemical group C1=CC=CC=C1C1=CC=CC(C=2C=CC=CC=2)=C1 YJTKZCDBKVTVBY-UHFFFAOYSA-N 0.000 claims 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims 1
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 claims 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims 1
- 239000005977 Ethylene Substances 0.000 claims 1
- AVXURJPOCDRRFD-UHFFFAOYSA-N Hydroxylamine Chemical compound ON AVXURJPOCDRRFD-UHFFFAOYSA-N 0.000 claims 1
- ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical group OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 claims 1
- 125000000641 acridinyl group Chemical group C1(=CC=CC2=NC3=CC=CC=C3C=C12)* 0.000 claims 1
- 125000003342 alkenyl group Chemical group 0.000 claims 1
- 150000001412 amines Chemical class 0.000 claims 1
- 125000005428 anthryl group Chemical group [H]C1=C([H])C([H])=C2C([H])=C3C(*)=C([H])C([H])=C([H])C3=C([H])C2=C1[H] 0.000 claims 1
- 125000005605 benzo group Chemical group 0.000 claims 1
- 125000004618 benzofuryl group Chemical group O1C(=CC2=C1C=CC=C2)* 0.000 claims 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims 1
- 125000006267 biphenyl group Chemical group 0.000 claims 1
- 125000000609 carbazolyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3NC12)* 0.000 claims 1
- 150000001768 cations Chemical class 0.000 claims 1
- 125000001309 chloro group Chemical group Cl* 0.000 claims 1
- 125000000259 cinnolinyl group Chemical group N1=NC(=CC2=CC=CC=C12)* 0.000 claims 1
- 239000003086 colorant Substances 0.000 claims 1
- 125000004093 cyano group Chemical group *C#N 0.000 claims 1
- 125000000000 cycloalkoxy group Chemical group 0.000 claims 1
- 125000005201 cycloalkylcarbonyloxy group Chemical group 0.000 claims 1
- 125000004987 dibenzofuryl group Chemical group C1(=CC=CC=2OC3=C(C21)C=CC=C3)* 0.000 claims 1
- 239000000975 dye Substances 0.000 claims 1
- 125000003983 fluorenyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3CC12)* 0.000 claims 1
- 125000003838 furazanyl group Chemical group 0.000 claims 1
- 125000002541 furyl group Chemical group 0.000 claims 1
- 125000001183 hydrocarbyl group Chemical group 0.000 claims 1
- 125000000743 hydrocarbylene group Chemical group 0.000 claims 1
- 150000002443 hydroxylamines Chemical class 0.000 claims 1
- 125000002883 imidazolyl group Chemical group 0.000 claims 1
- 125000003453 indazolyl group Chemical group N1N=C(C2=C1C=CC=C2)* 0.000 claims 1
- 125000003406 indolizinyl group Chemical group C=1(C=CN2C=CC=CC12)* 0.000 claims 1
- 125000001041 indolyl group Chemical group 0.000 claims 1
- 125000000904 isoindolyl group Chemical group C=1(NC=C2C=CC=CC12)* 0.000 claims 1
- 125000005956 isoquinolyl group Chemical group 0.000 claims 1
- 125000001786 isothiazolyl group Chemical group 0.000 claims 1
- 125000000842 isoxazolyl group Chemical group 0.000 claims 1
- 239000002184 metal Substances 0.000 claims 1
- 239000000178 monomer Substances 0.000 claims 1
- SQDFHQJTAWCFIB-UHFFFAOYSA-N n-methylidenehydroxylamine Chemical compound ON=C SQDFHQJTAWCFIB-UHFFFAOYSA-N 0.000 claims 1
- 125000001624 naphthyl group Chemical group 0.000 claims 1
- 125000004593 naphthyridinyl group Chemical group N1=C(C=CC2=CC=CN=C12)* 0.000 claims 1
- 125000001820 oxy group Chemical group [*:1]O[*:2] 0.000 claims 1
- 125000005010 perfluoroalkyl group Chemical group 0.000 claims 1
- 125000005327 perimidinyl group Chemical group N1C(=NC2=CC=CC3=CC=CC1=C23)* 0.000 claims 1
- 125000004934 phenanthridinyl group Chemical group C1(=CC=CC2=NC=C3C=CC=CC3=C12)* 0.000 claims 1
- 125000004625 phenanthrolinyl group Chemical group N1=C(C=CC2=CC=C3C=CC=NC3=C12)* 0.000 claims 1
- 125000005561 phenanthryl group Chemical group 0.000 claims 1
- 125000001791 phenazinyl group Chemical group C1(=CC=CC2=NC3=CC=CC=C3N=C12)* 0.000 claims 1
- 125000001484 phenothiazinyl group Chemical group C1(=CC=CC=2SC3=CC=CC=C3NC12)* 0.000 claims 1
- 125000001644 phenoxazinyl group Chemical group C1(=CC=CC=2OC3=CC=CC=C3NC12)* 0.000 claims 1
- 125000000951 phenoxy group Chemical class [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims 1
- 125000002071 phenylalkoxy group Chemical group 0.000 claims 1
- 125000004592 phthalazinyl group Chemical group C1(=NN=CC2=CC=CC=C12)* 0.000 claims 1
- 239000000049 pigment Substances 0.000 claims 1
- 229920002401 polyacrylamide Polymers 0.000 claims 1
- 229920000573 polyethylene Polymers 0.000 claims 1
- 229920002451 polyvinyl alcohol Polymers 0.000 claims 1
- 125000001042 pteridinyl group Chemical group N1=C(N=CC2=NC=CN=C12)* 0.000 claims 1
- 125000000561 purinyl group Chemical group N1=C(N=C2N=CNC2=C1)* 0.000 claims 1
- 125000003373 pyrazinyl group Chemical group 0.000 claims 1
- 125000003226 pyrazolyl group Chemical group 0.000 claims 1
- 125000004076 pyridyl group Chemical group 0.000 claims 1
- 125000000714 pyrimidinyl group Chemical group 0.000 claims 1
- 125000002112 pyrrolidino group Chemical group [*]N1C([H])([H])C([H])([H])C([H])([H])C1([H])[H] 0.000 claims 1
- 125000000168 pyrrolyl group Chemical group 0.000 claims 1
- 125000002294 quinazolinyl group Chemical group N1=C(N=CC2=CC=CC=C12)* 0.000 claims 1
- 125000005493 quinolyl group Chemical group 0.000 claims 1
- 125000001567 quinoxalinyl group Chemical group N1=C(C=NC2=CC=CC=C12)* 0.000 claims 1
- 125000000547 substituted alkyl group Chemical group 0.000 claims 1
- 125000005650 substituted phenylene group Chemical group 0.000 claims 1
- 125000001834 xanthenyl group Chemical group C1=CC=CC=2OC3=CC=CC=C3C(C12)* 0.000 claims 1
- 238000004383 yellowing Methods 0.000 claims 1
- 0 CC1(*)Oc2c(*)c(C)c(C)c(*)c2C1(*)* Chemical compound CC1(*)Oc2c(*)c(C)c(C)c(*)c2C1(*)* 0.000 description 1
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US32794401P | 2001-10-09 | 2001-10-09 | |
| US33825301P | 2001-12-06 | 2001-12-06 | |
| US40015802P | 2002-08-01 | 2002-08-01 | |
| PCT/EP2002/010995 WO2003031507A2 (en) | 2001-10-09 | 2002-10-01 | Polyester and polyamide compositions of low residual aldehyde content |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2005504868A JP2005504868A (ja) | 2005-02-17 |
| JP2005504868A5 true JP2005504868A5 (cg-RX-API-DMAC7.html) | 2006-01-05 |
Family
ID=27406563
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2003534486A Ceased JP2005504868A (ja) | 2001-10-09 | 2002-10-01 | 低残留アルデヒド含量のポリエステル及びポリアミド組成物 |
Country Status (10)
| Country | Link |
|---|---|
| US (1) | US20050176859A1 (cg-RX-API-DMAC7.html) |
| EP (1) | EP1440117B1 (cg-RX-API-DMAC7.html) |
| JP (1) | JP2005504868A (cg-RX-API-DMAC7.html) |
| AT (1) | ATE349488T1 (cg-RX-API-DMAC7.html) |
| AU (1) | AU2002350471A1 (cg-RX-API-DMAC7.html) |
| CA (1) | CA2466240A1 (cg-RX-API-DMAC7.html) |
| DE (1) | DE60217151T2 (cg-RX-API-DMAC7.html) |
| ES (1) | ES2278068T3 (cg-RX-API-DMAC7.html) |
| TW (1) | TWI303646B (cg-RX-API-DMAC7.html) |
| WO (1) | WO2003031507A2 (cg-RX-API-DMAC7.html) |
Families Citing this family (20)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP4144008B2 (ja) * | 2001-08-13 | 2008-09-03 | チバ ホールディング インコーポレーテッド | 低残存アルデヒド含量のポリエステル組成物 |
| WO2004000923A1 (en) * | 2002-06-24 | 2003-12-31 | The Procter & Gamble Company | Food package |
| WO2005040261A1 (en) * | 2003-10-15 | 2005-05-06 | Polyone Corporation | Use of tocopherol to scavenge acetaldehyde in polyethylene terephthalate containers |
| GB0406482D0 (en) * | 2004-03-23 | 2004-04-28 | Colormatrix Europe Ltd | Thermoplastic polymer additive compositions |
| WO2010068710A2 (en) * | 2008-12-09 | 2010-06-17 | University Of Florida Research Foundation, Inc. | Kinase inhibitor compounds |
| EP2406320A1 (en) * | 2009-03-13 | 2012-01-18 | Basf Se | Stabilized blends of polyester and polyamide |
| WO2010103030A2 (en) | 2009-03-13 | 2010-09-16 | Basf Se | Stabilized blends of polyester and polyamide |
| JP5294943B2 (ja) * | 2009-03-30 | 2013-09-18 | シーシーアイ株式会社 | ソリッドタイヤの荷重判定方法 |
| WO2011068987A2 (en) * | 2009-12-04 | 2011-06-09 | Georgetown University | Compositions and methods for the treatment of giardiasis |
| CN102875489B (zh) * | 2012-09-17 | 2015-09-30 | 浙江大学 | 2,6-二叔丁基-4-(苯基-1-哌啶基甲基)-苯酚的制备方法 |
| US9650539B2 (en) | 2014-10-27 | 2017-05-16 | Eastman Chemical Company | Thermosetting compositions based on unsaturated polyesters and phenolic resins |
| US9598602B2 (en) * | 2014-11-13 | 2017-03-21 | Eastman Chemical Company | Thermosetting compositions based on phenolic resins and curable poleyester resins made with diketene or beta-ketoacetate containing compounds |
| US9487619B2 (en) | 2014-10-27 | 2016-11-08 | Eastman Chemical Company | Carboxyl functional curable polyesters containing tetra-alkyl cyclobutanediol |
| US20160340471A1 (en) | 2015-05-19 | 2016-11-24 | Eastman Chemical Company | Aliphatic polyester coating compositions containing tetramethyl cyclobutanediol |
| US20170088665A1 (en) | 2015-09-25 | 2017-03-30 | Eastman Chemical Company | POLYMERS CONTAINING CYCLOBUTANEDIOL AND 2,2 BIS(HYDROXYMETHYL) AlKYLCARBOXYLIC ACID |
| US9988553B2 (en) | 2016-02-22 | 2018-06-05 | Eastman Chemical Company | Thermosetting coating compositions |
| US10011737B2 (en) | 2016-03-23 | 2018-07-03 | Eastman Chemical Company | Curable polyester polyols and their use in thermosetting soft feel coating formulations |
| EP3700750B1 (en) | 2017-10-26 | 2025-07-23 | AdvanSix Resins & Chemicals LLC | Multilayer package structure for ozone scavenging |
| CN109354571A (zh) * | 2018-09-29 | 2019-02-19 | 大连理工大学 | 回收再利用哌啶制备4-苯亚甲基-2,6-二叔丁基-2,5-环己二烯-1-酮的方法 |
| CN109735099A (zh) * | 2018-12-27 | 2019-05-10 | 会通新材料(上海)有限公司 | 一种改善耐光老化特性的聚酰胺56组合物及其应用 |
Family Cites Families (21)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NL98864C (cg-RX-API-DMAC7.html) * | 1956-10-02 | |||
| ZA757702B (en) * | 1975-02-26 | 1976-11-24 | Grace W R & Co | Adjustable sealing device |
| DE2551634C3 (de) * | 1975-11-18 | 1980-07-17 | Bayer Ag, 5090 Leverkusen | Verfahren zur Herstellung von Isocyanuratgruppen aufweisenden Polyisocyanaten |
| US4361681A (en) * | 1980-11-03 | 1982-11-30 | The Goodyear Tire & Rubber Company | Polyethylene terephthalate having a reduced acetaldehyde generation rate |
| EP0061210B1 (en) * | 1981-03-20 | 1985-01-16 | Akzo N.V. | Coloured polyethylene terephthalate moulding compound, a process for the preparation thereof and a container made therefrom |
| US4837115A (en) * | 1986-07-30 | 1989-06-06 | Toyo Seikan Kaisha, Ltd. | Thermoplastic polyester composition having improved flavor-retaining property and vessel formed therefrom |
| US4873279A (en) * | 1986-12-22 | 1989-10-10 | General Electric Company | Copolyester-carbonate and polyester resin blends exhibiting improved color properties |
| US5258233A (en) * | 1992-04-02 | 1993-11-02 | Eastman Kodak Company | Polyester/polyamide blend having improved flavor retaining property and clarity |
| US5266413A (en) * | 1992-05-18 | 1993-11-30 | Eastman Kodak Company | Copolyester/polyamide blend having improved flavor retaining property and clarity |
| KR940011606A (ko) * | 1992-11-05 | 1994-06-21 | 에른스트 알테르 | α,ω-알칸디페놀, 이를 함유하는 조성물 및 이들의 안정화제로서의 용도 |
| EP0691370A3 (en) * | 1994-07-07 | 1996-07-17 | Mitsubishi Chem Corp | Flame retardant polyester blend |
| US5459224A (en) * | 1994-07-18 | 1995-10-17 | Eastman Chemical Company | Copolyesters having improved weatherability |
| DE19503053B4 (de) * | 1995-02-01 | 2005-08-18 | Zimmer Ag | Verfahren zur direkten Herstellung von Polyester-Verpackungen |
| US5648032A (en) * | 1995-08-01 | 1997-07-15 | Eastman Chemical Company | Process for producing polyester articles having low acetaldehyde content |
| US5650469A (en) * | 1995-10-25 | 1997-07-22 | Eastman Chemical Company | Polyester/polyamide blend having improved flavor retaining property and clarity |
| DE19614067A1 (de) * | 1996-04-09 | 1997-10-16 | Hoechst Ag | Additivmischung mit nukleierender Wirkung für Kunststoffmassen |
| US6042908A (en) * | 1996-08-22 | 2000-03-28 | Eastman Chemical Company | Process for improving the flavor retaining property of polyester/polyamide blend containers for ozonated water |
| US6417358B1 (en) * | 1998-06-25 | 2002-07-09 | Ciba Specialty Chemicals Corporation | Process for the preparation of 3-aryl-benzofuranones |
| GB9909956D0 (en) * | 1999-04-29 | 1999-06-30 | Univ Aston | Thermoplastic moulding compositions and polymer additives |
| ATE339471T1 (de) * | 1999-06-30 | 2006-10-15 | Ciba Sc Holding Ag | Polyesterzusammensetzungen mit niedrigem restaldehydgehalt |
| US6274212B1 (en) * | 2000-02-22 | 2001-08-14 | The Coca-Cola Company | Method to decrease the acetaldehyde content of melt-processed polyesters |
-
2002
- 2002-10-01 AU AU2002350471A patent/AU2002350471A1/en not_active Abandoned
- 2002-10-01 JP JP2003534486A patent/JP2005504868A/ja not_active Ceased
- 2002-10-01 DE DE60217151T patent/DE60217151T2/de not_active Expired - Lifetime
- 2002-10-01 AT AT02785142T patent/ATE349488T1/de active
- 2002-10-01 WO PCT/EP2002/010995 patent/WO2003031507A2/en not_active Ceased
- 2002-10-01 ES ES02785142T patent/ES2278068T3/es not_active Expired - Lifetime
- 2002-10-01 US US10/491,598 patent/US20050176859A1/en not_active Abandoned
- 2002-10-01 CA CA002466240A patent/CA2466240A1/en not_active Abandoned
- 2002-10-01 EP EP02785142A patent/EP1440117B1/en not_active Expired - Lifetime
- 2002-10-07 TW TW091123048A patent/TWI303646B/zh not_active IP Right Cessation
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