JP2006519916A5 - - Google Patents
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- JP2006519916A5 JP2006519916A5 JP2006509020A JP2006509020A JP2006519916A5 JP 2006519916 A5 JP2006519916 A5 JP 2006519916A5 JP 2006509020 A JP2006509020 A JP 2006509020A JP 2006509020 A JP2006509020 A JP 2006509020A JP 2006519916 A5 JP2006519916 A5 JP 2006519916A5
- Authority
- JP
- Japan
- Prior art keywords
- alkyl
- substituted
- cycloalkyl
- mol
- residues
- 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.)
- Pending
Links
- 229910052739 hydrogen Inorganic materials 0.000 claims description 140
- 239000001257 hydrogen Substances 0.000 claims description 140
- 125000000217 alkyl group Chemical group 0.000 claims description 45
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 34
- 229910052757 nitrogen Inorganic materials 0.000 claims description 31
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 25
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 5
- 125000004573 morpholin-4-yl group Chemical group N1(CCOCC1)* 0.000 claims description 5
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 claims description 4
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 4
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 claims 152
- 150000002431 hydrogen Chemical class 0.000 claims 104
- 239000000203 mixture Substances 0.000 claims 79
- 150000002009 diols Chemical class 0.000 claims 74
- QPFMBZIOSGYJDE-UHFFFAOYSA-N 1,1,2,2-tetrachloroethane Chemical compound ClC(Cl)C(Cl)Cl QPFMBZIOSGYJDE-UHFFFAOYSA-N 0.000 claims 64
- 125000003118 aryl group Chemical group 0.000 claims 42
- 125000001072 heteroaryl group Chemical group 0.000 claims 40
- 229920000728 polyester Polymers 0.000 claims 40
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical group OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims 37
- KKEYFWRCBNTPAC-UHFFFAOYSA-N terephthalic acid group Chemical group C(C1=CC=C(C(=O)O)C=C1)(=O)O KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 claims 37
- 150000002894 organic compounds Chemical class 0.000 claims 35
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims 33
- 125000000753 cycloalkyl group Chemical group 0.000 claims 30
- 125000004433 nitrogen atom Chemical group N* 0.000 claims 29
- YIMQCDZDWXUDCA-UHFFFAOYSA-N [4-(hydroxymethyl)cyclohexyl]methanol Chemical group OCC1CCC(CO)CC1 YIMQCDZDWXUDCA-UHFFFAOYSA-N 0.000 claims 27
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical group OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 claims 26
- 150000003839 salts Chemical class 0.000 claims 25
- 150000001875 compounds Chemical class 0.000 claims 24
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 22
- -1 nitrogen-containing compound Chemical class 0.000 claims 22
- 125000004437 phosphorous atom Chemical group 0.000 claims 21
- 125000004406 C3-C8 cycloalkylene group Chemical group 0.000 claims 20
- 125000000732 arylene group Chemical group 0.000 claims 20
- 229910052698 phosphorus Inorganic materials 0.000 claims 20
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims 19
- 239000011574 phosphorus Substances 0.000 claims 19
- 229920000642 polymer Polymers 0.000 claims 18
- 230000002378 acidificating effect Effects 0.000 claims 17
- 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 claims 16
- ORLQHILJRHBSAY-UHFFFAOYSA-N [1-(hydroxymethyl)cyclohexyl]methanol Chemical group OCC1(CO)CCCCC1 ORLQHILJRHBSAY-UHFFFAOYSA-N 0.000 claims 11
- 125000004356 hydroxy functional group Chemical group O* 0.000 claims 10
- 125000005647 linker group Chemical group 0.000 claims 10
- 125000001424 substituent group Chemical group 0.000 claims 8
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims 6
- 229910052736 halogen Inorganic materials 0.000 claims 6
- 150000002367 halogens Chemical class 0.000 claims 6
- 239000006097 ultraviolet radiation absorber Substances 0.000 claims 5
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims 4
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 claims 4
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims 4
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical group C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims 4
- 229910052744 lithium Inorganic materials 0.000 claims 4
- 229920000515 polycarbonate Polymers 0.000 claims 4
- 239000004417 polycarbonate Substances 0.000 claims 4
- 229910052700 potassium Inorganic materials 0.000 claims 4
- 239000011591 potassium Substances 0.000 claims 4
- 229910052708 sodium Inorganic materials 0.000 claims 4
- 239000011734 sodium Substances 0.000 claims 4
- KZNICNPSHKQLFF-UHFFFAOYSA-N succinimide Chemical group O=C1CCC(=O)N1 KZNICNPSHKQLFF-UHFFFAOYSA-N 0.000 claims 4
- UDQTXCHQKHIQMH-KYGLGHNPSA-N (3ar,5s,6s,7r,7ar)-5-(difluoromethyl)-2-(ethylamino)-5,6,7,7a-tetrahydro-3ah-pyrano[3,2-d][1,3]thiazole-6,7-diol Chemical compound S1C(NCC)=N[C@H]2[C@@H]1O[C@H](C(F)F)[C@@H](O)[C@@H]2O UDQTXCHQKHIQMH-KYGLGHNPSA-N 0.000 claims 3
- 239000006096 absorbing agent Substances 0.000 claims 3
- 229910000147 aluminium phosphate Inorganic materials 0.000 claims 3
- 229940125936 compound 42 Drugs 0.000 claims 3
- 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 claims 3
- YSUIQYOGTINQIN-UZFYAQMZSA-N 2-amino-9-[(1S,6R,8R,9S,10R,15R,17R,18R)-8-(6-aminopurin-9-yl)-9,18-difluoro-3,12-dihydroxy-3,12-bis(sulfanylidene)-2,4,7,11,13,16-hexaoxa-3lambda5,12lambda5-diphosphatricyclo[13.2.1.06,10]octadecan-17-yl]-1H-purin-6-one Chemical compound NC1=NC2=C(N=CN2[C@@H]2O[C@@H]3COP(S)(=O)O[C@@H]4[C@@H](COP(S)(=O)O[C@@H]2[C@@H]3F)O[C@H]([C@H]4F)N2C=NC3=C2N=CN=C3N)C(=O)N1 YSUIQYOGTINQIN-UZFYAQMZSA-N 0.000 claims 2
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims 2
- 229910019142 PO4 Inorganic materials 0.000 claims 2
- 239000003963 antioxidant agent Substances 0.000 claims 2
- 230000003078 antioxidant effect Effects 0.000 claims 2
- 239000003054 catalyst Substances 0.000 claims 2
- 150000002148 esters Chemical class 0.000 claims 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 2
- 229910052751 metal Inorganic materials 0.000 claims 2
- 239000002184 metal Substances 0.000 claims 2
- 239000002530 phenolic antioxidant Substances 0.000 claims 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 claims 2
- 239000010452 phosphate Substances 0.000 claims 2
- 229920000137 polyphosphoric acid Polymers 0.000 claims 2
- PXGZQGDTEZPERC-UHFFFAOYSA-N 1,4-cyclohexanedicarboxylic acid Chemical group OC(=O)C1CCC(C(O)=O)CC1 PXGZQGDTEZPERC-UHFFFAOYSA-N 0.000 claims 1
- ZYUVGYBAPZYKSA-UHFFFAOYSA-N 5-(3-hydroxybutan-2-yl)-4-methylbenzene-1,3-diol Chemical compound CC(O)C(C)C1=CC(O)=CC(O)=C1C ZYUVGYBAPZYKSA-UHFFFAOYSA-N 0.000 claims 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims 1
- 239000003795 chemical substances by application Substances 0.000 claims 1
- NHADDZMCASKINP-HTRCEHHLSA-N decarboxydihydrocitrinin Natural products C1=C(O)C(C)=C2[C@H](C)[C@@H](C)OCC2=C1O NHADDZMCASKINP-HTRCEHHLSA-N 0.000 claims 1
- 0 Cc(cc(*)cc1Sc2cc(*)cc(*)c2O)c1O Chemical compound Cc(cc(*)cc1Sc2cc(*)cc(*)c2O)c1O 0.000 description 7
- 239000000126 substance Substances 0.000 description 4
- OWXXKGVQBCBSFJ-UHFFFAOYSA-N 6-n-[3-[[4,6-bis[butyl-(1,2,2,6,6-pentamethylpiperidin-4-yl)amino]-1,3,5-triazin-2-yl]-[2-[[4,6-bis[butyl-(1,2,2,6,6-pentamethylpiperidin-4-yl)amino]-1,3,5-triazin-2-yl]-[3-[[4,6-bis[butyl-(1,2,2,6,6-pentamethylpiperidin-4-yl)amino]-1,3,5-triazin-2-yl]ami Chemical compound N=1C(NCCCN(CCN(CCCNC=2N=C(N=C(N=2)N(CCCC)C2CC(C)(C)N(C)C(C)(C)C2)N(CCCC)C2CC(C)(C)N(C)C(C)(C)C2)C=2N=C(N=C(N=2)N(CCCC)C2CC(C)(C)N(C)C(C)(C)C2)N(CCCC)C2CC(C)(C)N(C)C(C)(C)C2)C=2N=C(N=C(N=2)N(CCCC)C2CC(C)(C)N(C)C(C)(C)C2)N(CCCC)C2CC(C)(C)N(C)C(C)(C)C2)=NC(N(CCCC)C2CC(C)(C)N(C)C(C)(C)C2)=NC=1N(CCCC)C1CC(C)(C)N(C)C(C)(C)C1 OWXXKGVQBCBSFJ-UHFFFAOYSA-N 0.000 description 3
- 150000007514 bases Chemical class 0.000 description 2
- XITRBUPOXXBIJN-UHFFFAOYSA-N bis(2,2,6,6-tetramethylpiperidin-4-yl) decanedioate Chemical compound C1C(C)(C)NC(C)(C)CC1OC(=O)CCCCCCCCC(=O)OC1CC(C)(C)NC(C)(C)C1 XITRBUPOXXBIJN-UHFFFAOYSA-N 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 125000003161 (C1-C6) alkylene group Chemical group 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 239000004611 light stabiliser Substances 0.000 description 1
- 229910017464 nitrogen compound Inorganic materials 0.000 description 1
- 150000002830 nitrogen compounds Chemical class 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US45232003P | 2003-03-05 | 2003-03-05 | |
| US10/393,475 US20040192813A1 (en) | 2003-03-20 | 2003-03-20 | Polymer compositions containing an ultraviolet light absorbing compound |
| PCT/US2004/006435 WO2004078840A2 (en) | 2003-03-05 | 2004-03-03 | Polymer compositions containing an ultraviolet light absorbing compound |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2006519916A JP2006519916A (ja) | 2006-08-31 |
| JP2006519916A5 true JP2006519916A5 (enExample) | 2006-10-12 |
Family
ID=32965335
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2006509020A Pending JP2006519916A (ja) | 2003-03-05 | 2004-03-03 | 紫外線吸収性化合物を含むポリマー組成物 |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US7491760B2 (enExample) |
| EP (1) | EP1599532B1 (enExample) |
| JP (1) | JP2006519916A (enExample) |
| KR (1) | KR101158123B1 (enExample) |
| BR (1) | BRPI0407952A (enExample) |
| WO (1) | WO2004078840A2 (enExample) |
Families Citing this family (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7550599B2 (en) * | 2003-02-26 | 2009-06-23 | Ciba Specialty Chemicals Corporation | Water compatible sterically hindered alkoxyamines and hydroxy substituted alkoxyamines |
| JP2007521378A (ja) * | 2003-07-11 | 2007-08-02 | イーストマン ケミカル カンパニー | 最大歩留りのためのｐｅｔプロセスへのｕｖ吸収剤の添加 |
| US7541407B2 (en) | 2004-05-27 | 2009-06-02 | Eastman Chemical Company | Process for adding methine UV light absorbers to PET prepared by direct esterification |
| JP2008503646A (ja) * | 2004-06-22 | 2008-02-07 | インヴィスタ テクノロジー エスアエルエル | 酸性および塩基性成分を含む可溶化添加剤組成物 |
| JP2012041467A (ja) * | 2010-08-20 | 2012-03-01 | Mitsubishi Chemicals Corp | ポリカーボネート樹脂組成物及び成形品 |
| JP6282792B2 (ja) * | 2010-08-20 | 2018-02-21 | 三菱ケミカル株式会社 | ポリカーボネート樹脂組成物及び成形品 |
| EP2511341A4 (en) * | 2009-12-10 | 2015-07-08 | Mitsubishi Chem Corp | POLYCARBONATE RESIN COMPOSITION AND MOLDING PRODUCTS |
| JP6151471B2 (ja) * | 2010-08-20 | 2017-06-21 | 三菱ケミカル株式会社 | ポリカーボネート樹脂組成物及び成形品 |
| KR101814832B1 (ko) * | 2009-12-10 | 2018-01-30 | 미쯔비시 케미컬 주식회사 | 폴리카보네이트 수지 조성물 그리고 이것을 성형하여 얻어지는 성형체, 필름, 플레이트 및 사출 성형품 |
| EP2511342A4 (en) * | 2009-12-10 | 2015-09-23 | Mitsubishi Chem Corp | POLYCARBONATE RESIN COMPOSITION AND MOLDING PRODUCTS |
| JP6151470B2 (ja) * | 2010-08-20 | 2017-06-21 | 三菱ケミカル株式会社 | ポリカーボネート樹脂組成物及び成形品 |
| JP5966251B2 (ja) | 2010-03-26 | 2016-08-10 | 三菱化学株式会社 | ポリカーボネート樹脂組成物及び成形品 |
| JP2016121365A (ja) * | 2016-04-04 | 2016-07-07 | 三菱化学株式会社 | ポリカーボネート樹脂組成物及び成形品 |
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-
2004
- 2004-03-03 JP JP2006509020A patent/JP2006519916A/ja active Pending
- 2004-03-03 EP EP04716911.5A patent/EP1599532B1/en not_active Expired - Lifetime
- 2004-03-03 WO PCT/US2004/006435 patent/WO2004078840A2/en not_active Ceased
- 2004-03-03 KR KR1020057016533A patent/KR101158123B1/ko not_active Expired - Fee Related
- 2004-03-03 BR BRPI0407952-3A patent/BRPI0407952A/pt not_active IP Right Cessation
-
2005
- 2005-08-16 US US11/204,461 patent/US7491760B2/en active Active
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