JP2000302758A5 - - Google Patents
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- JP2000302758A5 JP2000302758A5 JP2000049615A JP2000049615A JP2000302758A5 JP 2000302758 A5 JP2000302758 A5 JP 2000302758A5 JP 2000049615 A JP2000049615 A JP 2000049615A JP 2000049615 A JP2000049615 A JP 2000049615A JP 2000302758 A5 JP2000302758 A5 JP 2000302758A5
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- JP
- Japan
- Prior art keywords
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- carbon atoms
- alkyl
- hydroxy
- substituted
- 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 118
- 125000000217 alkyl group Chemical group 0.000 description 46
- 125000002252 acyl group Chemical group 0.000 description 24
- -1 2,3-dihydroxypropyl group Chemical group 0.000 description 22
- 125000001931 aliphatic group Chemical group 0.000 description 18
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 18
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 14
- 125000003073 divalent carboacyl group Chemical group 0.000 description 14
- 125000002947 alkylene group Chemical group 0.000 description 13
- 239000002253 acid Substances 0.000 description 12
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 11
- 125000003545 alkoxy group Chemical group 0.000 description 8
- KXDHJXZQYSOELW-UHFFFAOYSA-N carbonic acid monoamide Natural products NC(O)=O KXDHJXZQYSOELW-UHFFFAOYSA-N 0.000 description 8
- 150000001875 compounds Chemical class 0.000 description 8
- 239000000203 mixture Substances 0.000 description 8
- KJAMZCVTJDTESW-UHFFFAOYSA-N tiracizine Chemical compound C1CC2=CC=CC=C2N(C(=O)CN(C)C)C2=CC(NC(=O)OCC)=CC=C21 KJAMZCVTJDTESW-UHFFFAOYSA-N 0.000 description 8
- 125000002993 cycloalkylene group Chemical group 0.000 description 5
- 125000002723 alicyclic group Chemical group 0.000 description 4
- 150000007933 aliphatic carboxylic acids Chemical class 0.000 description 4
- 125000003342 alkenyl group Chemical group 0.000 description 4
- 150000001412 amines Chemical class 0.000 description 4
- 125000003118 aryl group Chemical group 0.000 description 4
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 4
- 125000005724 cycloalkenylene group Chemical group 0.000 description 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 4
- MSXVEPNJUHWQHW-UHFFFAOYSA-N 2-methylbutan-2-ol Chemical compound CCC(C)(C)O MSXVEPNJUHWQHW-UHFFFAOYSA-N 0.000 description 3
- JLIRPTLQJRCPCP-UHFFFAOYSA-N 6-o-[1-(2-hydroxy-2-methylpropoxy)-2,2,6,6-tetramethylpiperidin-4-yl] 1-o-methyl hexanedioate Chemical compound COC(=O)CCCCC(=O)OC1CC(C)(C)N(OCC(C)(C)O)C(C)(C)C1 JLIRPTLQJRCPCP-UHFFFAOYSA-N 0.000 description 3
- 125000004450 alkenylene group Chemical group 0.000 description 3
- 125000003277 amino group Chemical group 0.000 description 3
- 229910052799 carbon Inorganic materials 0.000 description 3
- 239000007795 chemical reaction product Substances 0.000 description 3
- 229910052801 chlorine Inorganic materials 0.000 description 3
- 125000001309 chloro group Chemical group Cl* 0.000 description 3
- 239000007859 condensation product Substances 0.000 description 3
- 125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 3
- 125000004430 oxygen atom Chemical group O* 0.000 description 3
- HJIAMFHSAAEUKR-UHFFFAOYSA-N (2-hydroxyphenyl)-phenylmethanone Chemical compound OC1=CC=CC=C1C(=O)C1=CC=CC=C1 HJIAMFHSAAEUKR-UHFFFAOYSA-N 0.000 description 2
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 description 2
- CSGAUKGQUCHWDP-UHFFFAOYSA-N 1-hydroxy-2,2,6,6-tetramethylpiperidin-4-ol Chemical compound CC1(C)CC(O)CC(C)(C)N1O CSGAUKGQUCHWDP-UHFFFAOYSA-N 0.000 description 2
- RKMGAJGJIURJSJ-UHFFFAOYSA-N 2,2,6,6-Tetramethylpiperidine Substances CC1(C)CCCC(C)(C)N1 RKMGAJGJIURJSJ-UHFFFAOYSA-N 0.000 description 2
- AXLQXVPJPNKKAF-UHFFFAOYSA-N C=C.C=C.C=C.C=C.C=C.C=C.N=C=O.N=C=O Chemical compound C=C.C=C.C=C.C=C.C=C.C=C.N=C=O.N=C=O AXLQXVPJPNKKAF-UHFFFAOYSA-N 0.000 description 2
- HPEUJPJOZXNMSJ-UHFFFAOYSA-N Methyl stearate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OC HPEUJPJOZXNMSJ-UHFFFAOYSA-N 0.000 description 2
- 239000007983 Tris buffer Substances 0.000 description 2
- 239000006096 absorbing agent Substances 0.000 description 2
- 125000003302 alkenyloxy group Chemical group 0.000 description 2
- 125000003282 alkyl amino group Chemical group 0.000 description 2
- 125000005530 alkylenedioxy group Chemical group 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- OPHOTHVVXMTDSN-UHFFFAOYSA-N bis[1-(2-hydroxy-2-methylpropoxy)-2,2,6,6-tetramethylpiperidin-4-yl] butanedioate Chemical compound C1C(C)(C)N(OCC(C)(O)C)C(C)(C)CC1OC(=O)CCC(=O)OC1CC(C)(C)N(OCC(C)(C)O)C(C)(C)C1 OPHOTHVVXMTDSN-UHFFFAOYSA-N 0.000 description 2
- WUXGYZUOHKJTEY-UHFFFAOYSA-N bis[1-(2-hydroxy-2-methylpropoxy)-2,2,6,6-tetramethylpiperidin-4-yl] hexanedioate Chemical compound C1C(C)(C)N(OCC(C)(O)C)C(C)(C)CC1OC(=O)CCCCC(=O)OC1CC(C)(C)N(OCC(C)(C)O)C(C)(C)C1 WUXGYZUOHKJTEY-UHFFFAOYSA-N 0.000 description 2
- JZOVJZCIRCQDDU-UHFFFAOYSA-N bis[1-(2-hydroxy-2-methylpropoxy)-2,2,6,6-tetramethylpiperidin-4-yl] pentanedioate Chemical compound C1C(C)(C)N(OCC(C)(O)C)C(C)(C)CC1OC(=O)CCCC(=O)OC1CC(C)(C)N(OCC(C)(C)O)C(C)(C)C1 JZOVJZCIRCQDDU-UHFFFAOYSA-N 0.000 description 2
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 description 2
- 239000000975 dye Substances 0.000 description 2
- 239000003063 flame retardant Substances 0.000 description 2
- 125000004029 hydroxymethyl group Chemical group [H]OC([H])([H])* 0.000 description 2
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 2
- 239000011976 maleic acid Substances 0.000 description 2
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 229920000620 organic polymer Polymers 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 125000004817 pentamethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[*:1] 0.000 description 2
- 125000000612 phthaloyl group Chemical group C(C=1C(C(=O)*)=CC=CC1)(=O)* 0.000 description 2
- 125000000587 piperidin-1-yl group Chemical group [H]C1([H])N(*)C([H])([H])C([H])([H])C([H])([H])C1([H])[H] 0.000 description 2
- 229920006395 saturated elastomer Polymers 0.000 description 2
- 125000003808 silyl group Chemical group [H][Si]([H])([H])[*] 0.000 description 2
- 230000000087 stabilizing effect Effects 0.000 description 2
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 2
- 125000006702 (C1-C18) alkyl group Chemical group 0.000 description 1
- YAXWOADCWUUUNX-UHFFFAOYSA-N 1,2,2,3-tetramethylpiperidine Chemical compound CC1CCCN(C)C1(C)C YAXWOADCWUUUNX-UHFFFAOYSA-N 0.000 description 1
- FYQOHJWNKFULEZ-UHFFFAOYSA-N 1-(2-hydroxy-2-methylpropoxy)-2,2,6,6-tetramethylpiperidin-4-ol Chemical compound CC(C)(O)CON1C(C)(C)CC(O)CC1(C)C FYQOHJWNKFULEZ-UHFFFAOYSA-N 0.000 description 1
- HAAOVMBCJOWJNT-UHFFFAOYSA-N 1-(2-hydroxyethoxy)-2,2,6,6-tetramethylpiperidin-4-ol Chemical compound CC1(C)CC(O)CC(C)(C)N1OCCO HAAOVMBCJOWJNT-UHFFFAOYSA-N 0.000 description 1
- NTGLWSXCQSEMIJ-UHFFFAOYSA-N 10-o-[1-(2-hydroxy-2-methylpropoxy)-2,2,6,6-tetramethylpiperidin-4-yl] 1-o-methyl decanedioate Chemical compound COC(=O)CCCCCCCCC(=O)OC1CC(C)(C)N(OCC(C)(C)O)C(C)(C)C1 NTGLWSXCQSEMIJ-UHFFFAOYSA-N 0.000 description 1
- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical class N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 description 1
- HWRLEEPNFJNTOP-UHFFFAOYSA-N 2-(1,3,5-triazin-2-yl)phenol Chemical compound OC1=CC=CC=C1C1=NC=NC=N1 HWRLEEPNFJNTOP-UHFFFAOYSA-N 0.000 description 1
- FJGQBLRYBUAASW-UHFFFAOYSA-N 2-(benzotriazol-2-yl)phenol Chemical compound OC1=CC=CC=C1N1N=C2C=CC=CC2=N1 FJGQBLRYBUAASW-UHFFFAOYSA-N 0.000 description 1
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 description 1
- DYIZJUDNMOIZQO-UHFFFAOYSA-N 4,5,6,7-tetrabromo-2-[2-(4,5,6,7-tetrabromo-1,3-dioxoisoindol-2-yl)ethyl]isoindole-1,3-dione Chemical compound O=C1C(C(=C(Br)C(Br)=C2Br)Br)=C2C(=O)N1CCN1C(=O)C2=C(Br)C(Br)=C(Br)C(Br)=C2C1=O DYIZJUDNMOIZQO-UHFFFAOYSA-N 0.000 description 1
- UWDMKTDPDJCJOP-UHFFFAOYSA-N 4-hydroxy-2,2,6,6-tetramethylpiperidin-1-ium-4-carboxylate Chemical compound CC1(C)CC(O)(C(O)=O)CC(C)(C)N1 UWDMKTDPDJCJOP-UHFFFAOYSA-N 0.000 description 1
- FJKROLUGYXJWQN-UHFFFAOYSA-M 4-hydroxybenzoate Chemical compound OC1=CC=C(C([O-])=O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-M 0.000 description 1
- MYHQQNGOMHTYGO-UHFFFAOYSA-N 4-o-[1-(2-hydroxy-2-methylpropoxy)-2,2,6,6-tetramethylpiperidin-4-yl] 1-o-methyl butanedioate Chemical compound COC(=O)CCC(=O)OC1CC(C)(C)N(OCC(C)(C)O)C(C)(C)C1 MYHQQNGOMHTYGO-UHFFFAOYSA-N 0.000 description 1
- DVTMIZHDLQFKEL-UHFFFAOYSA-N 5-o-[1-(2-hydroxy-2-methylpropoxy)-2,2,6,6-tetramethylpiperidin-4-yl] 1-o-methyl pentanedioate Chemical compound COC(=O)CCCC(=O)OC1CC(C)(C)N(OCC(C)(C)O)C(C)(C)C1 DVTMIZHDLQFKEL-UHFFFAOYSA-N 0.000 description 1
- 125000002853 C1-C4 hydroxyalkyl group Chemical group 0.000 description 1
- 241000790917 Dioxys <bee> Species 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 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
- 239000005057 Hexamethylene diisocyanate Substances 0.000 description 1
- AVXURJPOCDRRFD-UHFFFAOYSA-N Hydroxylamine Chemical compound ON AVXURJPOCDRRFD-UHFFFAOYSA-N 0.000 description 1
- DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 description 1
- XSTXAVWGXDQKEL-UHFFFAOYSA-N Trichloroethylene Chemical compound ClC=C(Cl)Cl XSTXAVWGXDQKEL-UHFFFAOYSA-N 0.000 description 1
- BRIAWAVIJRNLPF-UHFFFAOYSA-N [1-(2-hexadecanoyloxy-2-methylpropoxy)-2,2,6,6-tetramethylpiperidin-4-yl] hexadecanoate Chemical compound CCCCCCCCCCCCCCCC(=O)OC1CC(C)(C)N(OCC(C)(C)OC(=O)CCCCCCCCCCCCCCC)C(C)(C)C1 BRIAWAVIJRNLPF-UHFFFAOYSA-N 0.000 description 1
- ZEUWNUJMLBBCQQ-UHFFFAOYSA-N [1-(2-hydroxy-2-methylpropoxy)-2,2,6,6-tetramethylpiperidin-4-yl] hexadecanoate Chemical compound CCCCCCCCCCCCCCCC(=O)OC1CC(C)(C)N(OCC(C)(C)O)C(C)(C)C1 ZEUWNUJMLBBCQQ-UHFFFAOYSA-N 0.000 description 1
- KGUHWHHMNQPSRV-UHFFFAOYSA-N [1-(2-hydroxy-2-methylpropoxy)-2,2,6,6-tetramethylpiperidin-4-yl] octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OC1CC(C)(C)N(OCC(C)(C)O)C(C)(C)C1 KGUHWHHMNQPSRV-UHFFFAOYSA-N 0.000 description 1
- FLMHVBLPVFVUTM-UHFFFAOYSA-N [2,2,6,6-tetramethyl-1-(2-methyl-2-octadecanoyloxypropoxy)piperidin-4-yl] octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OC1CC(C)(C)N(OCC(C)(C)OC(=O)CCCCCCCCCCCCCCCCC)C(C)(C)C1 FLMHVBLPVFVUTM-UHFFFAOYSA-N 0.000 description 1
- 125000005336 allyloxy group Chemical group 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- DVXRGUXKOSSOHV-UHFFFAOYSA-N bis[1-(2-hydroxy-2-methylpropoxy)-2,2,6,6-tetramethylpiperidin-4-yl] decanedioate Chemical compound C1C(C)(C)N(OCC(C)(O)C)C(C)(C)CC1OC(=O)CCCCCCCCC(=O)OC1CC(C)(C)N(OCC(C)(C)O)C(C)(C)C1 DVXRGUXKOSSOHV-UHFFFAOYSA-N 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 150000007973 cyanuric acids Chemical class 0.000 description 1
- 125000000392 cycloalkenyl group Chemical group 0.000 description 1
- 125000000753 cycloalkyl group Chemical group 0.000 description 1
- HPXRVTGHNJAIIH-UHFFFAOYSA-N cyclohexanol Chemical compound OC1CCCCC1 HPXRVTGHNJAIIH-UHFFFAOYSA-N 0.000 description 1
- WHHGLZMJPXIBIX-UHFFFAOYSA-N decabromodiphenyl ether Chemical compound BrC1=C(Br)C(Br)=C(Br)C(Br)=C1OC1=C(Br)C(Br)=C(Br)C(Br)=C1Br WHHGLZMJPXIBIX-UHFFFAOYSA-N 0.000 description 1
- CAMHHLOGFDZBBG-UHFFFAOYSA-N epoxidized methyl oleate Natural products CCCCCCCCC1OC1CCCCCCCC(=O)OC CAMHHLOGFDZBBG-UHFFFAOYSA-N 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- JFCQEDHGNNZCLN-UHFFFAOYSA-N glutaric acid Chemical compound OC(=O)CCCC(O)=O JFCQEDHGNNZCLN-UHFFFAOYSA-N 0.000 description 1
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 150000002432 hydroperoxides Chemical class 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 239000003446 ligand Substances 0.000 description 1
- 239000004611 light stabiliser Substances 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 125000001160 methoxycarbonyl group Chemical group [H]C([H])([H])OC(*)=O 0.000 description 1
- 125000004573 morpholin-4-yl group Chemical group N1(CCOCC1)* 0.000 description 1
- FTWUXYZHDFCGSV-UHFFFAOYSA-N n,n'-diphenyloxamide Chemical compound C=1C=CC=CC=1NC(=O)C(=O)NC1=CC=CC=C1 FTWUXYZHDFCGSV-UHFFFAOYSA-N 0.000 description 1
- 125000004433 nitrogen atom Chemical group N* 0.000 description 1
- 125000000962 organic group Chemical group 0.000 description 1
- 150000002903 organophosphorus compounds Chemical class 0.000 description 1
- AQIXEPGDORPWBJ-UHFFFAOYSA-N pentan-3-ol Chemical compound CCC(O)CC AQIXEPGDORPWBJ-UHFFFAOYSA-N 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 125000000075 primary alcohol group Chemical group 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 150000003333 secondary alcohols Chemical class 0.000 description 1
- 125000004469 siloxy group Chemical group [SiH3]O* 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 150000003509 tertiary alcohols Chemical class 0.000 description 1
- 238000005809 transesterification reaction Methods 0.000 description 1
- BHYQWBKCXBXPKM-UHFFFAOYSA-N tris[3-bromo-2,2-bis(bromomethyl)propyl] phosphate Chemical compound BrCC(CBr)(CBr)COP(=O)(OCC(CBr)(CBr)CBr)OCC(CBr)(CBr)CBr BHYQWBKCXBXPKM-UHFFFAOYSA-N 0.000 description 1
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US09/257,711 US6271377B1 (en) | 1999-02-25 | 1999-02-25 | Hydroxy-substituted N-alkoxy hindered amines and compositions stabilized therewith |
| US09/315704 | 1999-05-20 | ||
| US09/257711 | 1999-05-20 | ||
| US09/315,704 US6166212A (en) | 1999-05-20 | 1999-05-20 | Process for the synthesis of N-(hydroxyalkoxy) substituted hindered amine stabilizers |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2000302758A JP2000302758A (ja) | 2000-10-31 |
| JP2000302758A5 true JP2000302758A5 (enrdf_load_stackoverflow) | 2007-04-12 |
| JP4757977B2 JP4757977B2 (ja) | 2011-08-24 |
Family
ID=26946156
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2000049615A Expired - Lifetime JP4757977B2 (ja) | 1999-02-25 | 2000-02-25 | ヒドロキシ−置換されたｎ−アルコキシ立体障害性アミン |
Country Status (18)
Families Citing this family (37)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB2377935B (en) * | 1998-12-14 | 2003-06-18 | Ciba Sc Holding Ag | Sterically hindered amine compounds |
| US6376584B1 (en) * | 1999-02-25 | 2002-04-23 | Ciba Specialty Chemicals Corporation | Hydroxy-substituted N-alkoxy hindered amines and compositions stabilized therewith |
| TWI273115B (en) * | 2000-12-12 | 2007-02-11 | Ciba Sc Holding Ag | Improved weatherability of flame retardant polyolefin |
| DE10106543A1 (de) * | 2001-02-13 | 2002-08-22 | Basf Ag | Beschichtungsmittelzusammensetzungen |
| US20030040593A1 (en) * | 2001-04-26 | 2003-02-27 | Nobuya Saegusa | Vinyl-polymerizable monomer having tertiary hydroxyl group and polymer |
| JP4562324B2 (ja) * | 2001-07-06 | 2010-10-13 | 株式会社Adeka | 安定化されたポリウレタン樹脂 |
| ITMI20012081A1 (it) * | 2001-10-09 | 2003-04-09 | 3V Sigma Spa | Composizioni liquide di perossidi stabilizzate |
| CA2517334A1 (en) * | 2003-02-26 | 2004-09-10 | Ciba Specialty Chemicals Holding Inc. | Water compatible sterically hindered alkoxyamines and hydroxy substituted alkoxyamines |
| CN1823042B (zh) * | 2003-07-14 | 2010-06-23 | 西巴特殊化学品控股有限公司 | 制备位阻n-烃氧基胺类化合物的过氧化氢催化的方法 |
| US7595011B2 (en) | 2004-07-12 | 2009-09-29 | Ciba Specialty Chemicals Corporation | Stabilized electrochromic media |
| US7410936B2 (en) * | 2004-08-23 | 2008-08-12 | Ciba Specialty Chemicals Corporation | Stabilized body care products, household products, textiles and fabrics |
| WO2007007855A1 (ja) * | 2005-07-08 | 2007-01-18 | Canon Kabushiki Kaisha | サーマルインクジェット用インク及びそれを用いたインクカートリッジ |
| CN101218103B (zh) * | 2005-07-08 | 2011-07-13 | 佳能株式会社 | 热喷墨墨和使用该墨的墨盒 |
| US20070072965A1 (en) * | 2005-09-23 | 2007-03-29 | Mouhcine Kanouni | Color fast polyurethanes |
| CN101484423B (zh) * | 2006-07-05 | 2011-09-07 | 西巴控股有限公司 | 制备位阻硝酰基醚的方法 |
| US8481726B2 (en) | 2006-07-05 | 2013-07-09 | Basf Se | Process for the preparation of sterically hindered nitroxyl ethers |
| ATE493387T1 (de) | 2006-07-05 | 2011-01-15 | Basf Se | Verfahren zur herstellung sterisch gehinderter nitroxylether |
| US20120145241A1 (en) * | 2009-08-18 | 2012-06-14 | Basf Se | Photovoltaic module with stabilized polymeric encapsulant |
| EP2708574A1 (en) * | 2012-09-18 | 2014-03-19 | Clariant International Ltd. | Oxygen scavenging plastic material |
| NZ718820A (en) | 2013-09-30 | 2017-10-27 | Certain Teed Corp | Stain repellent and voc eliminating coatings and use thereof |
| SG11201606231TA (en) | 2014-02-28 | 2016-08-30 | Exxonmobil Chem Patents Inc | Mooney viscosity stable brominated elastomers |
| SA116370295B1 (ar) * | 2015-02-20 | 2016-12-06 | باسف اس اى | رقائق، وأشرطة وفتائل أحادية من البولي أوليفين مثبتة للضوء |
| WO2017015338A1 (en) * | 2015-07-20 | 2017-01-26 | Basf Corporation | Flame-retardant polyolefin systems |
| CN105085376B (zh) * | 2015-09-07 | 2018-01-05 | 江苏裕兴薄膜科技股份有限公司 | 一种含受阻胺基团的二元醇单体及其聚酯共聚物 |
| US10767073B2 (en) * | 2016-10-18 | 2020-09-08 | Ppg Industries Ohio, Inc. | Curable film-forming compositions containing hydroxyl functional, branched acrylic polymers and multilayer composite coatings |
| KR102201293B1 (ko) * | 2019-05-15 | 2021-01-11 | 한국신발피혁연구원 | 웨더 스트립용 우레탄 아크릴레이트계 하이브리드 코팅 조성물 |
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| CN110606986B (zh) * | 2019-09-20 | 2020-05-22 | 杭州聚丰新材料有限公司 | 一种硅橡胶交联剂及其制备方法与应用 |
| CN110903237A (zh) * | 2019-12-16 | 2020-03-24 | 兰州精细化工有限责任公司 | 一种双(1-辛氧基-2,2,6,6-四甲基-4-哌啶基)癸二酸酯的制备方法 |
| EP4083168A4 (en) | 2019-12-27 | 2024-01-10 | Daihachi Chemical Industry Co., Ltd. | FLAME RETARDANT COMPOSITION AND FLAME RETARDANT THERMOPLASTIC RESIN COMPOSITION HAVING THE FLAME RETARDANT COMPOSITION |
| CN112778990B (zh) * | 2021-02-05 | 2022-06-03 | 西南石油大学 | 一种用于油田注水井的污水混配暂堵剂及其制备方法 |
| CN113582914B (zh) * | 2021-08-02 | 2023-11-03 | 天津利安隆新材料股份有限公司 | 含羟基的受阻胺光稳定剂的制备方法 |
| KR102497017B1 (ko) * | 2021-08-26 | 2023-02-07 | 강남제비스코 주식회사 | LiDAR 기능 향상을 위한 아크릴폴리올계 서페이서 조성물 |
| CN113956776B (zh) * | 2021-12-06 | 2022-12-13 | 烟台大学 | 可粉末化自修复阻燃低voc聚氨酯涂料的制备方法及汽车革中应用 |
| CN114940684B (zh) * | 2022-05-24 | 2023-07-21 | 浙江大学温州研究院 | 一种白光发光的卤化铜配合物及其制备方法和应用 |
| CN116082705B (zh) * | 2022-12-05 | 2023-09-12 | 苏州易昇光学材料股份有限公司 | 一种抗黄变自修复凝胶 |
| EP4464752A1 (de) * | 2023-05-17 | 2024-11-20 | Lignocolor GmbH | Verfahren zur beschichtung von harten oberflächen mit pigmentfilmen |
Family Cites Families (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU571240B2 (en) * | 1983-07-11 | 1988-04-14 | Commonwealth Scientific And Industrial Research Organisation | Alkoxy-amines, useful as initiators |
| SU1215332A3 (ru) * | 1983-12-27 | 1999-02-10 | Научно - исследовательский институт химикатов для полимерных материалов. | Олигомеры на основе эпоксидных смол и производных пространственно-затрудненных аминов в качестве светостабилизирующей добавки к термостабилизатору полипропилена на основе фенольных антиоксидантов |
| EP0155912A3 (de) * | 1984-03-20 | 1986-06-04 | Ciba-Geigy Ag | Strahlenstabilisierte polymere Zusammensetzungen |
| US5096950A (en) * | 1988-10-19 | 1992-03-17 | Ciba-Geigy Corporation | Polyolefin compositions stabilized with NOR-substituted hindered amines |
| EP0365481A1 (en) * | 1988-10-19 | 1990-04-25 | Ciba-Geigy Ag | Polymeric substrates stabilized with N-substituted hindered amines |
| US5004770A (en) * | 1988-10-19 | 1991-04-02 | Ciba-Geigy Corporation | Polymeric substrates stabilized with N-substituted hindered amines |
| EP0389420B1 (en) * | 1989-03-21 | 1994-09-21 | Ciba-Geigy Ag | Ethylenically unsaturated compounds containing 1-hydrocarbyloxy-2,2,6,6-tetramethylpiperidine moieties, and polymers, copolymers and stabilized compositions |
| IT1237126B (it) * | 1989-11-07 | 1993-05-18 | Ciba Geigy Spa | Stabilizzanti polimerici contenenti gruppi amminici impediti e gruppi idrossilamminici |
| TW270131B (enrdf_load_stackoverflow) * | 1993-07-13 | 1996-02-11 | Ciba Geigy | |
| JPH0952975A (ja) * | 1995-08-18 | 1997-02-25 | Clariant Internatl Ltd | 顔料の安定化方法及びこの方法に用いる組成物 |
| US5627248A (en) * | 1995-09-26 | 1997-05-06 | The Dow Chemical Company | Difunctional living free radical polymerization initiators |
| US5844025A (en) * | 1996-12-02 | 1998-12-01 | Ciba Specialty Chemicals Corporation | 1,2-Bis-adducts of stable nitroxides with substituted ethylenes and stabilized compositions |
| TW509683B (en) * | 1997-05-27 | 2002-11-11 | Ciba Sc Holding Ag | Triazine derivatives containing 2,2,6,6-tetramethyl-4-piperidyl groups |
| ATE284862T1 (de) * | 1999-06-23 | 2005-01-15 | Nof Corp | Vinylierte alkoxamine, ihre verwendung und ein verfahren zu ihrer herstellung |
| DE50004231D1 (de) * | 1999-09-07 | 2003-12-04 | Bayer Ag | Funktionalisierte Alkoxyamin-Initiatoren |
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2000
- 2000-02-15 GB GBGB0003326.6A patent/GB0003326D0/en not_active Ceased
- 2000-02-17 NL NL1014414A patent/NL1014414C2/nl not_active IP Right Cessation
- 2000-02-23 DE DE10008367.6A patent/DE10008367B4/de not_active Expired - Lifetime
- 2000-02-23 IT IT2000MI000327A patent/IT1319167B1/it active
- 2000-02-23 TW TW089103127A patent/TW491876B/zh not_active IP Right Cessation
- 2000-02-23 ES ES200000419A patent/ES2195674B1/es not_active Expired - Fee Related
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- 2000-02-24 FR FR0002308A patent/FR2790259B1/fr not_active Expired - Lifetime
- 2000-02-24 KR KR1020000009171A patent/KR100676473B1/ko not_active Expired - Lifetime
- 2000-02-24 CN CNB001065157A patent/CN1230424C/zh not_active Expired - Lifetime
- 2000-02-24 BE BE2000/0146A patent/BE1013530A5/fr not_active IP Right Cessation
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