JP2003522242A5 - - Google Patents
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- JP2003522242A5 JP2003522242A5 JP2001557952A JP2001557952A JP2003522242A5 JP 2003522242 A5 JP2003522242 A5 JP 2003522242A5 JP 2001557952 A JP2001557952 A JP 2001557952A JP 2001557952 A JP2001557952 A JP 2001557952A JP 2003522242 A5 JP2003522242 A5 JP 2003522242A5
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- JP
- Japan
- Prior art keywords
- group
- carbon atoms
- substituted
- alkyl
- branched
- 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.)
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- 125000004432 carbon atom Chemical group C* 0.000 description 112
- 125000000217 alkyl group Chemical group 0.000 description 43
- 125000002947 alkylene group Chemical group 0.000 description 24
- 125000000753 cycloalkyl group Chemical group 0.000 description 18
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 18
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 18
- 125000003342 alkenyl group Chemical group 0.000 description 14
- 125000003884 phenylalkyl group Chemical group 0.000 description 13
- 125000003118 aryl group Chemical group 0.000 description 10
- -1 3-oxapentamethylene Chemical group 0.000 description 9
- 125000005843 halogen group Chemical group 0.000 description 9
- 239000000203 mixture Substances 0.000 description 8
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 description 8
- 229910052799 carbon Inorganic materials 0.000 description 7
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 7
- 239000004033 plastic Substances 0.000 description 6
- 229920003023 plastic Polymers 0.000 description 6
- 125000003710 aryl alkyl group Chemical group 0.000 description 5
- 125000003545 alkoxy group Chemical group 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- 125000002993 cycloalkylene group Chemical group 0.000 description 4
- ZCILGMFPJBRCNO-UHFFFAOYSA-N 4-phenyl-2H-benzotriazol-5-ol Chemical compound OC1=CC=C2NN=NC2=C1C1=CC=CC=C1 ZCILGMFPJBRCNO-UHFFFAOYSA-N 0.000 description 3
- RWRDLPDLKQPQOW-UHFFFAOYSA-N Pyrrolidine Chemical compound C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 description 3
- 125000004956 cyclohexylene group Chemical group 0.000 description 3
- 125000004209 (C1-C8) alkyl group Chemical group 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 description 2
- NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 description 2
- 125000004453 alkoxycarbonyl group Chemical group 0.000 description 2
- 125000000732 arylene group Chemical group 0.000 description 2
- 125000004429 atom Chemical group 0.000 description 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 2
- 125000004093 cyano group Chemical group *C#N 0.000 description 2
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 2
- 125000003700 epoxy group Chemical group 0.000 description 2
- 125000000816 ethylene group Chemical group [H]C([H])([*:1])C([H])([H])[*:2] 0.000 description 2
- 125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 125000002768 hydroxyalkyl group Chemical group 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 125000001624 naphthyl group Chemical group 0.000 description 2
- 125000004433 nitrogen atom Chemical group N* 0.000 description 2
- 239000005022 packaging material Substances 0.000 description 2
- 125000005010 perfluoroalkyl group Chemical group 0.000 description 2
- 125000004193 piperazinyl group Chemical group 0.000 description 2
- 239000006097 ultraviolet radiation absorber Substances 0.000 description 2
- 125000003837 (C1-C20) alkyl group Chemical group 0.000 description 1
- LEVFXWNQQSSNAC-UHFFFAOYSA-N 2-(4,6-diphenyl-1,3,5-triazin-2-yl)-5-hexoxyphenol Chemical compound OC1=CC(OCCCCCC)=CC=C1C1=NC(C=2C=CC=CC=2)=NC(C=2C=CC=CC=2)=N1 LEVFXWNQQSSNAC-UHFFFAOYSA-N 0.000 description 1
- UWSMKYBKUPAEJQ-UHFFFAOYSA-N 5-Chloro-2-(3,5-di-tert-butyl-2-hydroxyphenyl)-2H-benzotriazole Chemical compound CC(C)(C)C1=CC(C(C)(C)C)=CC(N2N=C3C=C(Cl)C=CC3=N2)=C1O UWSMKYBKUPAEJQ-UHFFFAOYSA-N 0.000 description 1
- HWUPDMFSGDXFMI-UHFFFAOYSA-N C1CCCCC1.[C] Chemical group C1CCCCC1.[C] HWUPDMFSGDXFMI-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical group C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 description 1
- 239000002250 absorbent Substances 0.000 description 1
- 230000002745 absorbent Effects 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 125000002252 acyl group Chemical group 0.000 description 1
- 125000004442 acylamino group Chemical group 0.000 description 1
- 125000004423 acyloxy group Chemical group 0.000 description 1
- 150000001335 aliphatic alkanes Chemical class 0.000 description 1
- 125000004450 alkenylene group Chemical group 0.000 description 1
- 125000003282 alkyl amino group Chemical group 0.000 description 1
- 125000004419 alkynylene group Chemical group 0.000 description 1
- 125000001769 aryl amino group Chemical group 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- QRUDEWIWKLJBPS-UHFFFAOYSA-N benzotriazole Chemical compound C1=CC=C2N[N][N]C2=C1 QRUDEWIWKLJBPS-UHFFFAOYSA-N 0.000 description 1
- 239000012964 benzotriazole Substances 0.000 description 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
- 125000000649 benzylidene group Chemical group [H]C(=[*])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
- 125000002619 bicyclic group Chemical group 0.000 description 1
- 125000005569 butenylene group Chemical group 0.000 description 1
- 125000005622 butynylene group Chemical group 0.000 description 1
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- 125000000392 cycloalkenyl group Chemical group 0.000 description 1
- 125000000000 cycloalkoxy group Chemical group 0.000 description 1
- 125000006840 diphenylmethane group Chemical group 0.000 description 1
- 125000002541 furyl group Chemical group 0.000 description 1
- 125000001188 haloalkyl group Chemical group 0.000 description 1
- 230000009931 harmful effect Effects 0.000 description 1
- 150000002430 hydrocarbons Chemical group 0.000 description 1
- 125000002757 morpholinyl group Chemical group 0.000 description 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 125000004430 oxygen atom Chemical group O* 0.000 description 1
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 1
- 125000003386 piperidinyl group Chemical group 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- 125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 description 1
- 125000005628 tolylene group Chemical group 0.000 description 1
- 125000006839 xylylene group Chemical group 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US17956700P | 2000-02-01 | 2000-02-01 | |
| US60/179,567 | 2000-02-01 | ||
| PCT/EP2001/000694 WO2001057124A2 (en) | 2000-02-01 | 2001-01-23 | Method of content protection with durable uv absorbers |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2003522242A JP2003522242A (ja) | 2003-07-22 |
| JP2003522242A5 true JP2003522242A5 (enExample) | 2008-03-13 |
| JP4681193B2 JP4681193B2 (ja) | 2011-05-11 |
Family
ID=22657115
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2001557952A Expired - Fee Related JP4681193B2 (ja) | 2000-02-01 | 2001-01-23 | 耐久性紫外線吸収剤による内容物の保護方法 |
Country Status (13)
| Country | Link |
|---|---|
| US (4) | US20020028861A1 (enExample) |
| EP (1) | EP1252226B1 (enExample) |
| JP (1) | JP4681193B2 (enExample) |
| KR (1) | KR100689232B1 (enExample) |
| CN (1) | CN1180008C (enExample) |
| AT (1) | ATE353353T1 (enExample) |
| AU (1) | AU780351B2 (enExample) |
| BR (2) | BR0117305B1 (enExample) |
| CA (1) | CA2396221C (enExample) |
| DE (1) | DE60126476T8 (enExample) |
| MX (2) | MX229551B (enExample) |
| RU (1) | RU2266306C2 (enExample) |
| WO (1) | WO2001057124A2 (enExample) |
Families Citing this family (40)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2003070819A1 (en) * | 2002-02-19 | 2003-08-28 | Ciba Specialty Chemicals Holding Inc. | Containers or films comprising hydroxyphenlbenzotriazole uv absorbers for protecting contents against the effects of uv radiation |
| WO2004000921A1 (en) * | 2002-06-19 | 2003-12-31 | Ciba Specialty Chemicals Holding Inc. | Stabilized polyamide compositions |
| US8831966B2 (en) * | 2003-02-14 | 2014-09-09 | Oracle International Corporation | Method for delegated administration |
| US7591000B2 (en) | 2003-02-14 | 2009-09-15 | Oracle International Corporation | System and method for hierarchical role-based entitlements |
| US6917975B2 (en) * | 2003-02-14 | 2005-07-12 | Bea Systems, Inc. | Method for role and resource policy management |
| CA2523569A1 (en) * | 2003-05-06 | 2004-11-18 | Ciba Specialty Chemicals Holding Inc. | Photo-cured and stabilized coatings |
| JP2007507567A (ja) * | 2003-05-26 | 2007-03-29 | チバ スペシャルティ ケミカルズ ホールディング インコーポレーテッド | 高適合性及び非移行性ポリマー状ｕｖ−吸収剤 |
| US20060252857A1 (en) * | 2003-05-27 | 2006-11-09 | Schaefer Thomas | Aminoaryl-1-3-5-triazines and their use as uv absorbers |
| FR2856659B1 (fr) * | 2003-06-30 | 2005-09-23 | Brosserie Soc Gen De | Flacon chimiquement resistant pour produits cosmetiques. |
| US20050047991A1 (en) * | 2003-09-03 | 2005-03-03 | Rees Wayne M. | Method of stabilizing packaged active chlorine-containing solutions against light-induced degradation employing alkaline hypochlorite solutions in combination with a container |
| US20050047990A1 (en) * | 2003-09-03 | 2005-03-03 | Rees Wayne M. | Method of stabilizing packaged active chlorine-containing solutions against light-induced degradation employing stabilized hypochlorite solutions in combination with a container |
| US20050249904A1 (en) * | 2004-01-23 | 2005-11-10 | Rajnish Batlaw | Articles and process of making polypropylene articles having ultraviolet light protection by injection stretch blow molding of polypropylene |
| AU2005235601A1 (en) | 2004-04-16 | 2005-11-03 | Advanced Plastics Technologies Luxemboug S.A. | A bottle, a method of forming the bottle, a liquid dispensing system and an extruded profile |
| US20050232848A1 (en) * | 2004-04-20 | 2005-10-20 | Andreas Nguyen | Packaging for dilute hypochlorite |
| PL1865347T3 (pl) * | 2005-03-31 | 2012-10-31 | Nippon Catalytic Chem Ind | Polaryzacyjna folia ochronna, płytka polaryzacyjna, oraz wyświetlacz obrazu |
| US20070090010A1 (en) * | 2005-10-20 | 2007-04-26 | The Procter & Gamble Company | Transparent or translucent filled package exhibiting a colored appearance |
| WO2008006722A2 (en) * | 2006-07-10 | 2008-01-17 | Ciba Holding Inc. | Method of protecting organic material from light |
| TWI473851B (zh) * | 2008-07-22 | 2015-02-21 | Basell Polyolefine Gmbh | 在包含生質柴油及氧之液態燃料存在下具改良抗熱氧化降解力之乙烯聚合物及由其所製成之塑料燃料槽 |
| CH699237B1 (de) * | 2008-07-24 | 2011-07-15 | Alpla Werke | Kunststoffformulierung und Verfahren zur Herstellung von Kunststoffflaschen in einem Zweistufen-Streckblasprozess. |
| MY150926A (en) * | 2008-07-30 | 2014-03-14 | Colgate Palmolive Co | A uv-protected container with product having dyes or lakes |
| RU2371365C1 (ru) * | 2008-11-05 | 2009-10-27 | Игорь Александрович Зенов | Многослойная пластиковая емкость для хранения пищевых продуктов |
| EP2380859B1 (en) * | 2008-12-22 | 2018-08-22 | Sekisui Chemical Co., Ltd. | Laminate for laminated glass and interlayer for laminated glass |
| CN102292397B (zh) | 2009-01-19 | 2014-12-10 | 巴斯夫欧洲公司 | 有机黑色颜料及其制备 |
| JP5422269B2 (ja) | 2009-06-23 | 2014-02-19 | 富士フイルム株式会社 | 紫外線吸収剤組成物及び樹脂組成物 |
| RU2404102C1 (ru) * | 2009-06-29 | 2010-11-20 | Игорь Александрович Зенов | Пластиковая емкость для хранения пищевых продуктов (варианты) |
| EP2453874A2 (en) * | 2009-07-14 | 2012-05-23 | Biogen Idec MA Inc. | Methods for inhibiting yellow color and peroxide formation in a composition |
| US8216357B2 (en) * | 2009-09-25 | 2012-07-10 | General Electric Company | Protective coating compositions and devices |
| BR112012010588A2 (pt) * | 2009-11-05 | 2019-09-24 | Procter & Gamble | produto embalado destinado à proteção de composição líquida senível à luz. |
| FR2959494B1 (fr) | 2010-04-28 | 2014-01-03 | Soc Lotoise Devaporation Solev | Emballage rigide pour produit cosmetique ou pharmaceutique sensible au rayonnement ultraviolet |
| CN103930276A (zh) * | 2011-11-14 | 2014-07-16 | 电气化学工业株式会社 | 多层树脂片及成型容器 |
| US9244013B2 (en) * | 2012-06-29 | 2016-01-26 | Johnson & Johnson Vision Care, Inc. | Method of quantifying UV disinfecting doses applied to an ophthalmic lens using indicators |
| CN102944940B (zh) * | 2012-12-04 | 2014-07-30 | 吴金军 | 一种感光变色镜片 |
| JP2016033021A (ja) * | 2014-07-31 | 2016-03-10 | 株式会社Adeka | 紫外線遮光容器 |
| CN104495098A (zh) * | 2014-11-11 | 2015-04-08 | 句容市茂源织造厂 | 一种绿色蔬菜包装 |
| RU2624704C1 (ru) * | 2016-04-15 | 2017-07-05 | Общество с ограниченной ответственностью "Данафлекс-Нано" | Прозрачный высокобарьерный материал |
| RU2635136C1 (ru) * | 2016-08-30 | 2017-11-09 | Общество с ограниченной ответственностью "Терморан" (ООО "Терморан") | Стеклонаполненная композиция на основе полифениленсульфида |
| CN110563661B (zh) * | 2018-06-05 | 2021-08-27 | 台湾永光化学工业股份有限公司 | 具红移效应的苯并三唑紫外线吸收剂及其用途 |
| KR102769555B1 (ko) * | 2018-06-21 | 2025-02-19 | 도판 홀딩스 가부시키가이샤 | 보호 필름 및 시트 |
| GB2590495B (en) * | 2019-12-20 | 2024-08-28 | Henkel Ag & Co Kgaa | A container for, and a pack including, cyanoacrylate composition(s) |
| KR102866440B1 (ko) | 2020-07-28 | 2025-10-01 | 삼성디스플레이 주식회사 | 표시 장치 및 표시 장치용 광 흡수제 |
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| EP0913462A1 (en) | 1997-10-31 | 1999-05-06 | The Procter & Gamble Company | Liquid aqueous bleaching compositions packaged in a UV-resistant container |
| DE69941073D1 (de) | 1998-03-02 | 2009-08-20 | Ciba Holding Inc | Verfahren zur Herstellung von 2,4-Diaryl-6-o-hydroxyphenyl-1,3,5-triazin Derivaten in Anwesenheit eines Protonensäure-Katalysators |
| AR018847A1 (es) | 1998-04-09 | 2001-12-12 | Procter & Gamble | Producto detergente para el lavado de vajilla que tiene una botella resistente a la luz ultravioleta |
| DE69814096T2 (de) | 1998-11-10 | 2004-03-04 | The Procter & Gamble Company, Cincinnati | Folie mit Eigenschaften hinsichtlich UV-Barriere |
| WO2000043318A2 (en) | 1999-01-22 | 2000-07-27 | The Procter & Gamble Company | Colored acidic rinse aid product having an ultraviolet light resistant bottle |
| BR0010228A (pt) * | 1999-05-03 | 2002-02-13 | Ciba Sc Holding Ag | Composições adesivas estabilizadas contendo absorvedores de uv de benzotriazol fotoestáveis, deslocados para o vermelho, altamente solúveis e artigos laminados derivados das mesmas |
| US6191199B1 (en) * | 1999-05-03 | 2001-02-20 | Ciba Speciatly Chemicals Corporation | Stabilized adhesive compositions containing highly soluble, high extinction photostable hydroxyphenyl-s-triazine UV absorbers and laminated articles derived therefrom |
| EP1038912A3 (en) * | 2000-06-22 | 2000-12-27 | Ciba SC Holding AG | High molecular weight hindered hydrocarbyloxyamine stabilizers |
-
2001
- 2001-01-23 MX MXPA02007355 patent/MX229551B/es active IP Right Grant
- 2001-01-23 EP EP01916950A patent/EP1252226B1/en not_active Expired - Lifetime
- 2001-01-23 JP JP2001557952A patent/JP4681193B2/ja not_active Expired - Fee Related
- 2001-01-23 RU RU2002123360/04A patent/RU2266306C2/ru not_active IP Right Cessation
- 2001-01-23 AU AU44106/01A patent/AU780351B2/en not_active Ceased
- 2001-01-23 BR BRPI0117305-7A patent/BR0117305B1/pt not_active IP Right Cessation
- 2001-01-23 CN CNB018043992A patent/CN1180008C/zh not_active Expired - Fee Related
- 2001-01-23 AT AT01916950T patent/ATE353353T1/de active
- 2001-01-23 CA CA2396221A patent/CA2396221C/en not_active Expired - Fee Related
- 2001-01-23 BR BRPI0108013-0A patent/BR0108013B1/pt not_active IP Right Cessation
- 2001-01-23 DE DE60126476T patent/DE60126476T8/de active Active
- 2001-01-23 KR KR1020027009228A patent/KR100689232B1/ko not_active Expired - Fee Related
- 2001-01-23 WO PCT/EP2001/000694 patent/WO2001057124A2/en not_active Ceased
- 2001-01-29 US US09/772,245 patent/US20020028861A1/en not_active Abandoned
-
2002
- 2002-07-30 MX MXPA05001128 patent/MX257080A/es unknown
- 2002-11-15 US US10/295,313 patent/US6746739B2/en not_active Expired - Lifetime
- 2002-12-18 US US10/323,238 patent/US6797751B2/en not_active Expired - Lifetime
-
2004
- 2004-03-30 US US10/812,722 patent/US7288583B2/en not_active Expired - Fee Related
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