SK57597A3 - Use of 3-arylacrylic acid esters as light-protection agents and stabilizers for non-living organic material - Google Patents

Use of 3-arylacrylic acid esters as light-protection agents and stabilizers for non-living organic material Download PDF

Info

Publication number: SK57597A3
Authority: SK; Slovakia
Prior art keywords: acid esters; arylacrylic acid; symbols; light; carbon atoms
Prior art date: 1994-11-11

Application number

SK575-97A

Other languages

English (en)

Slovak (sk)

Inventor

Alexander Aumuller

Martin Holderbaum

Wolfgang Goetze

Jurgen Krockenberger

Hubert Trauth

Original Assignee

Basf Ag

Priority date (The priority date 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 date listed.)

1994-11-11

Filing date

1995-11-03

Publication date

1998-06-03

1995-11-03 Application filed by Basf Ag filed Critical Basf Ag

1998-06-03 Publication of SK57597A3 publication Critical patent/SK57597A3/sk

Links

239000002253 acid Substances 0.000 title claims abstract description 18
239000003381 stabilizer Substances 0.000 title claims abstract description 18
150000002148 esters Chemical class 0.000 title claims abstract description 17
239000011368 organic material Substances 0.000 title claims abstract description 17
239000011814 protection agent Substances 0.000 title abstract description 5
125000004432 carbon atom Chemical group C* 0.000 claims abstract description 16
125000004430 oxygen atom Chemical group O* 0.000 claims abstract description 9
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims abstract description 6
150000003077 polyols Chemical group 0.000 claims abstract description 6
229910052739 hydrogen Inorganic materials 0.000 claims abstract description 5
239000001257 hydrogen Substances 0.000 claims abstract description 5
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract description 4
125000003118 aryl group Chemical group 0.000 claims abstract description 4
-1 aliphatic polyol Chemical class 0.000 claims description 53
229920003023 plastic Polymers 0.000 claims description 12
125000000217 alkyl group Chemical group 0.000 claims description 11
239000004033 plastic Substances 0.000 claims description 11
229920005862 polyol Polymers 0.000 claims description 9
239000003973 paint Substances 0.000 claims description 8
239000004417 polycarbonate Substances 0.000 claims description 8
239000004922 lacquer Substances 0.000 claims description 7
229920000515 polycarbonate Polymers 0.000 claims description 7
229920002635 polyurethane Polymers 0.000 claims description 6
239000004814 polyurethane Substances 0.000 claims description 6
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 5
230000000087 stabilizing effect Effects 0.000 claims description 5
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 3
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 3
229910052760 oxygen Inorganic materials 0.000 claims description 3
239000001301 oxygen Substances 0.000 claims description 3
125000004172 4-methoxyphenyl group Chemical group [H]C1=C([H])C(OC([H])([H])[H])=C([H])C([H])=C1* 0.000 claims description 2
239000003223 protective agent Substances 0.000 claims description 2
125000003545 alkoxy group Chemical group 0.000 claims 1
125000005036 alkoxyphenyl group Chemical group 0.000 claims 1
239000011203 carbon fibre reinforced carbon Substances 0.000 claims 1
125000001931 aliphatic group Chemical group 0.000 abstract description 2
125000001424 substituent group Chemical group 0.000 abstract description 2
125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 1
150000001875 compounds Chemical class 0.000 description 23
150000001412 amines Chemical class 0.000 description 8
229920000642 polymer Polymers 0.000 description 7
DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 6
239000003963 antioxidant agent Substances 0.000 description 5
235000006708 antioxidants Nutrition 0.000 description 5
229920001577 copolymer Polymers 0.000 description 5
239000000463 material Substances 0.000 description 5
239000000203 mixture Substances 0.000 description 5
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 4
239000004676 acrylonitrile butadiene styrene Substances 0.000 description 4
WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 4
150000001993 dienes Chemical class 0.000 description 4
239000004611 light stabiliser Substances 0.000 description 4
238000004383 yellowing Methods 0.000 description 4
CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 3
229920005830 Polyurethane Foam Polymers 0.000 description 3
XECAHXYUAAWDEL-UHFFFAOYSA-N acrylonitrile butadiene styrene Chemical compound C=CC=C.C=CC#N.C=CC1=CC=CC=C1 XECAHXYUAAWDEL-UHFFFAOYSA-N 0.000 description 3
229920000122 acrylonitrile butadiene styrene Polymers 0.000 description 3
239000007859 condensation product Substances 0.000 description 3
125000002887 hydroxy group Chemical group [H]O* 0.000 description 3
150000005673 monoalkenes Chemical class 0.000 description 3
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 3
239000011496 polyurethane foam Substances 0.000 description 3
230000006641 stabilisation Effects 0.000 description 3
238000011105 stabilization Methods 0.000 description 3
GVJHHUAWPYXKBD-UHFFFAOYSA-N (±)-α-Tocopherol Chemical compound OC1=C(C)C(C)=C2OC(CCCC(C)CCCC(C)CCCC(C)C)(C)CCC2=C1C GVJHHUAWPYXKBD-UHFFFAOYSA-N 0.000 description 2
PZRWFKGUFWPFID-UHFFFAOYSA-N 3,9-dioctadecoxy-2,4,8,10-tetraoxa-3,9-diphosphaspiro[5.5]undecane Chemical compound C1OP(OCCCCCCCCCCCCCCCCCC)OCC21COP(OCCCCCCCCCCCCCCCCCC)OC2 PZRWFKGUFWPFID-UHFFFAOYSA-N 0.000 description 2
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 2
229940126062 Compound A Drugs 0.000 description 2
239000005977 Ethylene Substances 0.000 description 2
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 2
NLDMNSXOCDLTTB-UHFFFAOYSA-N Heterophylliin A Natural products O1C2COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC2C(OC(=O)C=2C=C(O)C(O)=C(O)C=2)C(O)C1OC(=O)C1=CC(O)=C(O)C(O)=C1 NLDMNSXOCDLTTB-UHFFFAOYSA-N 0.000 description 2
BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 2
PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 2
NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 description 2
GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 2
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 2
239000006096 absorbing agent Substances 0.000 description 2
239000000654 additive Substances 0.000 description 2
QRUDEWIWKLJBPS-UHFFFAOYSA-N benzotriazole Chemical class C1=CC=C2N[N][N]C2=C1 QRUDEWIWKLJBPS-UHFFFAOYSA-N 0.000 description 2
YWDBZVIHZORXHG-UHFFFAOYSA-N bis(2,2,6,6-tetramethylpiperidin-1-yl) decanedioate Chemical compound CC1(C)CCCC(C)(C)N1OC(=O)CCCCCCCCC(=O)ON1C(C)(C)CCCC1(C)C YWDBZVIHZORXHG-UHFFFAOYSA-N 0.000 description 2
ZCDOYSPFYFSLEW-UHFFFAOYSA-N chromate(2-) Chemical class [O-][Cr]([O-])(=O)=O ZCDOYSPFYFSLEW-UHFFFAOYSA-N 0.000 description 2
238000000576 coating method Methods 0.000 description 2
230000000052 comparative effect Effects 0.000 description 2
239000002537 cosmetic Substances 0.000 description 2
ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 2
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
239000008187 granular material Substances 0.000 description 2
ZFSLODLOARCGLH-UHFFFAOYSA-N isocyanuric acid Chemical compound OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 0.000 description 2
239000006078 metal deactivator Substances 0.000 description 2
229910052757 nitrogen Inorganic materials 0.000 description 2
229910052698 phosphorus Inorganic materials 0.000 description 2
239000011574 phosphorus Substances 0.000 description 2
229920000728 polyester Polymers 0.000 description 2
230000001681 protective effect Effects 0.000 description 2
150000003254 radicals Chemical class 0.000 description 2
239000000126 substance Substances 0.000 description 2
229910052717 sulfur Inorganic materials 0.000 description 2
239000011593 sulfur Substances 0.000 description 2
239000002966 varnish Substances 0.000 description 2
229920002554 vinyl polymer Polymers 0.000 description 2
WEXKMBZQRXRWGX-UHFFFAOYSA-N (2,2,6,6-tetramethylpiperidin-1-yl) 2-[bis[2-oxo-2-(2,2,6,6-tetramethylpiperidin-1-yl)oxyethyl]amino]acetate Chemical compound CC1(C)CCCC(C)(C)N1OC(=O)CN(CC(=O)ON1C(CCCC1(C)C)(C)C)CC(=O)ON1C(C)(C)CCCC1(C)C WEXKMBZQRXRWGX-UHFFFAOYSA-N 0.000 description 1
HJIAMFHSAAEUKR-UHFFFAOYSA-N (2-hydroxyphenyl)-phenylmethanone Chemical class OC1=CC=CC=C1C(=O)C1=CC=CC=C1 HJIAMFHSAAEUKR-UHFFFAOYSA-N 0.000 description 1
CDUQMGQIHYISOP-RMKNXTFCSA-N (e)-2-cyano-3-phenylprop-2-enoic acid Chemical class OC(=O)C(\C#N)=C\C1=CC=CC=C1 CDUQMGQIHYISOP-RMKNXTFCSA-N 0.000 description 1
FIDRAVVQGKNYQK-UHFFFAOYSA-N 1,2,3,4-tetrahydrotriazine Chemical compound C1NNNC=C1 FIDRAVVQGKNYQK-UHFFFAOYSA-N 0.000 description 1
VNQNXQYZMPJLQX-UHFFFAOYSA-N 1,3,5-tris[(3,5-ditert-butyl-4-hydroxyphenyl)methyl]-1,3,5-triazinane-2,4,6-trione Chemical compound CC(C)(C)C1=C(O)C(C(C)(C)C)=CC(CN2C(N(CC=3C=C(C(O)=C(C=3)C(C)(C)C)C(C)(C)C)C(=O)N(CC=3C=C(C(O)=C(C=3)C(C)(C)C)C(C)(C)C)C2=O)=O)=C1 VNQNXQYZMPJLQX-UHFFFAOYSA-N 0.000 description 1
HTSGKJQDMSTCGS-UHFFFAOYSA-N 1,4-bis(4-chlorophenyl)-2-(4-methylphenyl)sulfonylbutane-1,4-dione Chemical compound C1=CC(C)=CC=C1S(=O)(=O)C(C(=O)C=1C=CC(Cl)=CC=1)CC(=O)C1=CC=C(Cl)C=C1 HTSGKJQDMSTCGS-UHFFFAOYSA-N 0.000 description 1
JDLQSLMTBGPZLW-UHFFFAOYSA-N 1-(1-hydroxyethyl)-2,2,6,6-tetramethylpiperidin-4-ol Chemical compound CC(O)N1C(C)(C)CC(O)CC1(C)C JDLQSLMTBGPZLW-UHFFFAOYSA-N 0.000 description 1
IHBLBMDDUQOYLA-UHFFFAOYSA-N 1-octadecyl-3-[4-[[4-(octadecylcarbamoylamino)phenyl]methyl]phenyl]urea Chemical compound C1=CC(NC(=O)NCCCCCCCCCCCCCCCCCC)=CC=C1CC1=CC=C(NC(=O)NCCCCCCCCCCCCCCCCCC)C=C1 IHBLBMDDUQOYLA-UHFFFAOYSA-N 0.000 description 1
PNXIFUGGZQKIIT-UHFFFAOYSA-N 10-oxo-10-(2,2,3,3,4-pentamethylpiperidin-1-yl)oxydecanoic acid Chemical compound CC1CCN(C(C1(C)C)(C)C)OC(=O)CCCCCCCCC(=O)O PNXIFUGGZQKIIT-UHFFFAOYSA-N 0.000 description 1
FTVFPPFZRRKJIH-UHFFFAOYSA-N 2,2,6,6-tetramethylpiperidin-4-amine Chemical class CC1(C)CC(N)CC(C)(C)N1 FTVFPPFZRRKJIH-UHFFFAOYSA-N 0.000 description 1
125000004201 2,4-dichlorophenyl group Chemical group [H]C1=C([H])C(*)=C(Cl)C([H])=C1Cl 0.000 description 1
FJGQBLRYBUAASW-UHFFFAOYSA-N 2-(benzotriazol-2-yl)phenol Chemical class OC1=CC=CC=C1N1N=C2C=CC=CC2=N1 FJGQBLRYBUAASW-UHFFFAOYSA-N 0.000 description 1
PQJZHMCWDKOPQG-UHFFFAOYSA-N 2-anilino-2-oxoacetic acid Chemical class OC(=O)C(=O)NC1=CC=CC=C1 PQJZHMCWDKOPQG-UHFFFAOYSA-N 0.000 description 1
125000006276 2-bromophenyl group Chemical group [H]C1=C([H])C(Br)=C(*)C([H])=C1[H] 0.000 description 1
125000004182 2-chlorophenyl group Chemical group [H]C1=C([H])C(Cl)=C(*)C([H])=C1[H] 0.000 description 1
239000004808 2-ethylhexylester Substances 0.000 description 1
125000004198 2-fluorophenyl group Chemical group [H]C1=C([H])C(F)=C(*)C([H])=C1[H] 0.000 description 1
CNXZMGRWEYQCOQ-UHFFFAOYSA-N 2-methoxy-3-phenylprop-2-enoic acid Chemical compound COC(C(O)=O)=CC1=CC=CC=C1 CNXZMGRWEYQCOQ-UHFFFAOYSA-N 0.000 description 1
125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
HNTWDNMNGNBFEA-UHFFFAOYSA-N 3,3,5,5-tetramethylpiperazin-2-one Chemical compound CC1(C)CNC(=O)C(C)(C)N1 HNTWDNMNGNBFEA-UHFFFAOYSA-N 0.000 description 1
AIBRSVLEQRWAEG-UHFFFAOYSA-N 3,9-bis(2,4-ditert-butylphenoxy)-2,4,8,10-tetraoxa-3,9-diphosphaspiro[5.5]undecane Chemical compound CC(C)(C)C1=CC(C(C)(C)C)=CC=C1OP1OCC2(COP(OC=3C(=CC(=CC=3)C(C)(C)C)C(C)(C)C)OC2)CO1 AIBRSVLEQRWAEG-UHFFFAOYSA-N 0.000 description 1
125000006275 3-bromophenyl group Chemical group [H]C1=C([H])C(Br)=C([H])C(*)=C1[H] 0.000 description 1
125000004179 3-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C(Cl)=C1[H] 0.000 description 1
125000004180 3-fluorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C(F)=C1[H] 0.000 description 1
PRWJPWSKLXYEPD-UHFFFAOYSA-N 4-[4,4-bis(5-tert-butyl-4-hydroxy-2-methylphenyl)butan-2-yl]-2-tert-butyl-5-methylphenol Chemical compound C=1C(C(C)(C)C)=C(O)C=C(C)C=1C(C)CC(C=1C(=CC(O)=C(C=1)C(C)(C)C)C)C1=CC(C(C)(C)C)=C(O)C=C1C PRWJPWSKLXYEPD-UHFFFAOYSA-N 0.000 description 1
125000004800 4-bromophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Br 0.000 description 1
125000001255 4-fluorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1F 0.000 description 1
UQRONKZLYKUEMO-UHFFFAOYSA-N 4-methyl-1-(2,4,6-trimethylphenyl)pent-4-en-2-one Chemical group CC(=C)CC(=O)Cc1c(C)cc(C)cc1C UQRONKZLYKUEMO-UHFFFAOYSA-N 0.000 description 1
NLZUEZXRPGMBCV-UHFFFAOYSA-N Butylhydroxytoluene Chemical compound CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 NLZUEZXRPGMBCV-UHFFFAOYSA-N 0.000 description 1
UHRASWZLCRHSJE-UHFFFAOYSA-N CC1(NC(CC(C1)C(C(C(C(C(=O)O)(C1CC(NC(C1)(C)C)(C)C)C1CC(NC(C1)(C)C)(C)C)C(=O)O)C(=O)O)(C(=O)O)C1CC(NC(C1)(C)C)(C)C)(C)C)C Chemical compound CC1(NC(CC(C1)C(C(C(C(C(=O)O)(C1CC(NC(C1)(C)C)(C)C)C1CC(NC(C1)(C)C)(C)C)C(=O)O)C(=O)O)(C(=O)O)C1CC(NC(C1)(C)C)(C)C)(C)C)C UHRASWZLCRHSJE-UHFFFAOYSA-N 0.000 description 1
BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
GHKOFFNLGXMVNJ-UHFFFAOYSA-N Didodecyl thiobispropanoate Chemical compound CCCCCCCCCCCCOC(=O)CCSCCC(=O)OCCCCCCCCCCCC GHKOFFNLGXMVNJ-UHFFFAOYSA-N 0.000 description 1
239000003508 Dilauryl thiodipropionate Substances 0.000 description 1
239000002656 Distearyl thiodipropionate Substances 0.000 description 1
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
229920004011 Macrolon® Polymers 0.000 description 1
YBGZDTIWKVFICR-JLHYYAGUSA-N Octyl 4-methoxycinnamic acid Chemical compound CCCCC(CC)COC(=O)\C=C\C1=CC=C(OC)C=C1 YBGZDTIWKVFICR-JLHYYAGUSA-N 0.000 description 1
239000002033 PVDF binder Substances 0.000 description 1
JKIJEFPNVSHHEI-UHFFFAOYSA-N Phenol, 2,4-bis(1,1-dimethylethyl)-, phosphite (3:1) Chemical compound CC(C)(C)C1=CC(C(C)(C)C)=CC=C1OP(OC=1C(=CC(=CC=1)C(C)(C)C)C(C)(C)C)OC1=CC=C(C(C)(C)C)C=C1C(C)(C)C JKIJEFPNVSHHEI-UHFFFAOYSA-N 0.000 description 1
229920002319 Poly(methyl acrylate) Polymers 0.000 description 1
239000004952 Polyamide Substances 0.000 description 1
239000005062 Polybutadiene Substances 0.000 description 1
239000004743 Polypropylene Substances 0.000 description 1
229920002396 Polyurea Polymers 0.000 description 1
239000004372 Polyvinyl alcohol Substances 0.000 description 1
XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 1
KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 1
ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
229930003427 Vitamin E Natural products 0.000 description 1
YIMQCDZDWXUDCA-UHFFFAOYSA-N [4-(hydroxymethyl)cyclohexyl]methanol Chemical compound OCC1CCC(CO)CC1 YIMQCDZDWXUDCA-UHFFFAOYSA-N 0.000 description 1
150000007513 acids Chemical class 0.000 description 1
150000001252 acrylic acid derivatives Chemical class 0.000 description 1
NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
230000032683 aging Effects 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
125000003277 amino group Chemical group 0.000 description 1
239000002216 antistatic agent Substances 0.000 description 1
235000010290 biphenyl Nutrition 0.000 description 1
239000004305 biphenyl Substances 0.000 description 1
125000006269 biphenyl-2-yl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C1=C(*)C([H])=C([H])C([H])=C1[H] 0.000 description 1
125000006268 biphenyl-3-yl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C1=C([H])C(*)=C([H])C([H])=C1[H] 0.000 description 1
125000000319 biphenyl-4-yl group Chemical group [H]C1=C([H])C([H])=C([H])C([H])=C1C1=C([H])C([H])=C([*])C([H])=C1[H] 0.000 description 1
SMISHRXKWQZCCQ-UHFFFAOYSA-N bis(1,2,2,6,6-pentamethylpiperidin-3-yl) decanedioate Chemical compound CC1(C)N(C)C(C)(C)CCC1OC(=O)CCCCCCCCC(=O)OC1C(C)(C)N(C)C(C)(C)CC1 SMISHRXKWQZCCQ-UHFFFAOYSA-N 0.000 description 1
DQXBYHZEEUGOBF-UHFFFAOYSA-N but-3-enoic acid;ethene Chemical compound C=C.OC(=O)CC=C DQXBYHZEEUGOBF-UHFFFAOYSA-N 0.000 description 1
KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 description 1
235000010354 butylated hydroxytoluene Nutrition 0.000 description 1
230000015556 catabolic process Effects 0.000 description 1
238000002144 chemical decomposition reaction Methods 0.000 description 1
PMMYEEVYMWASQN-IMJSIDKUSA-N cis-4-Hydroxy-L-proline Chemical compound O[C@@H]1CN[C@H](C(O)=O)C1 PMMYEEVYMWASQN-IMJSIDKUSA-N 0.000 description 1
238000004040 coloring Methods 0.000 description 1
125000004122 cyclic group Chemical group 0.000 description 1
125000000753 cycloalkyl group Chemical group 0.000 description 1
125000000582 cycloheptyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
RLMGYIOTPQVQJR-UHFFFAOYSA-N cyclohexane-1,3-diol Chemical compound OC1CCCC(O)C1 RLMGYIOTPQVQJR-UHFFFAOYSA-N 0.000 description 1
UKJLNMAFNRKWGR-UHFFFAOYSA-N cyclohexatrienamine Chemical group NC1=CC=C=C[CH]1 UKJLNMAFNRKWGR-UHFFFAOYSA-N 0.000 description 1
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 1
125000000640 cyclooctyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C([H])([H])C1([H])[H] 0.000 description 1
NUUPJBRGQCEZSI-UHFFFAOYSA-N cyclopentane-1,3-diol Chemical compound OC1CCC(O)C1 NUUPJBRGQCEZSI-UHFFFAOYSA-N 0.000 description 1
125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
238000006731 degradation reaction Methods 0.000 description 1
235000019304 dilauryl thiodipropionate Nutrition 0.000 description 1
SZXQTJUDPRGNJN-UHFFFAOYSA-N dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 description 1
238000002845 discoloration Methods 0.000 description 1
PWWSSIYVTQUJQQ-UHFFFAOYSA-N distearyl thiodipropionate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)CCSCCC(=O)OCCCCCCCCCCCCCCCCCC PWWSSIYVTQUJQQ-UHFFFAOYSA-N 0.000 description 1
235000019305 distearyl thiodipropionate Nutrition 0.000 description 1
239000000839 emulsion Substances 0.000 description 1
229920006242 ethylene acrylic acid copolymer Polymers 0.000 description 1
125000000816 ethylene group Chemical group [H]C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
239000005038 ethylene vinyl acetate Substances 0.000 description 1
238000001125 extrusion Methods 0.000 description 1
239000000945 filler Substances 0.000 description 1
239000003063 flame retardant Substances 0.000 description 1
WIGCFUFOHFEKBI-UHFFFAOYSA-N gamma-tocopherol Natural products CC(C)CCCC(C)CCCC(C)CCCC1CCC2C(C)C(O)C(C)C(C)C2O1 WIGCFUFOHFEKBI-UHFFFAOYSA-N 0.000 description 1
229910052736 halogen Inorganic materials 0.000 description 1
125000005843 halogen group Chemical group 0.000 description 1
150000002367 halogens Chemical class 0.000 description 1
229920001903 high density polyethylene Polymers 0.000 description 1
239000004700 high-density polyethylene Substances 0.000 description 1
125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 1
125000001972 isopentyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 description 1
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
125000005644 linolenyl group Chemical group 0.000 description 1
239000007788 liquid Substances 0.000 description 1
230000007774 longterm Effects 0.000 description 1
229920001684 low density polyethylene Polymers 0.000 description 1
239000004702 low-density polyethylene Substances 0.000 description 1
125000000040 m-tolyl group Chemical group [H]C1=C([H])C(*)=C([H])C(=C1[H])C([H])([H])[H] 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
238000000034 method Methods 0.000 description 1
GPKUICFDWYEPTK-UHFFFAOYSA-N methoxycyclohexatriene Chemical compound COC1=CC=C=C[CH]1 GPKUICFDWYEPTK-UHFFFAOYSA-N 0.000 description 1
238000000465 moulding Methods 0.000 description 1
QITVMFSGIKQAFH-UHFFFAOYSA-N n'-(2,2,6,6-tetramethylpiperidin-1-yl)hexane-1,6-diamine Chemical compound CC1(C)CCCC(C)(C)N1NCCCCCCN QITVMFSGIKQAFH-UHFFFAOYSA-N 0.000 description 1
KZWQGEXECXCXPR-UHFFFAOYSA-N n-[6-formamido-6-(2,2,6,6-tetramethylpiperidin-4-yl)hexyl]formamide Chemical compound CC1(C)CC(C(CCCCCNC=O)NC=O)CC(C)(C)N1 KZWQGEXECXCXPR-UHFFFAOYSA-N 0.000 description 1
125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
125000003136 n-heptyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
125000001280 n-hexyl group Chemical group C(CCCCC)* 0.000 description 1
125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
XOZHJGPWRAFSMY-UHFFFAOYSA-N n-phenyl-1h-benzimidazole-2-carboxamide Chemical class N=1C2=CC=CC=C2NC=1C(=O)NC1=CC=CC=C1 XOZHJGPWRAFSMY-UHFFFAOYSA-N 0.000 description 1
125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
125000001624 naphthyl group Chemical group 0.000 description 1
230000007935 neutral effect Effects 0.000 description 1
229910052759 nickel Inorganic materials 0.000 description 1
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
XZPUTNZHTQVTHG-UHFFFAOYSA-N nonanethioic s-acid Chemical compound CCCCCCCCC(O)=S XZPUTNZHTQVTHG-UHFFFAOYSA-N 0.000 description 1
125000003261 o-tolyl group Chemical group [H]C1=C([H])C(*)=C(C([H])=C1[H])C([H])([H])[H] 0.000 description 1
SSDSCDGVMJFTEQ-UHFFFAOYSA-N octadecyl 3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)CCC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 SSDSCDGVMJFTEQ-UHFFFAOYSA-N 0.000 description 1
239000002674 ointment Substances 0.000 description 1
125000001117 oleyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])/C([H])=C([H])\C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 description 1
125000000636 p-nitrophenyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)[N+]([O-])=O 0.000 description 1
125000001037 p-tolyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])[H] 0.000 description 1
NFHFRUOZVGFOOS-UHFFFAOYSA-N palladium;triphenylphosphane Chemical compound [Pd].C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 NFHFRUOZVGFOOS-UHFFFAOYSA-N 0.000 description 1
239000008194 pharmaceutical composition Substances 0.000 description 1
239000002530 phenolic antioxidant Substances 0.000 description 1
150000002989 phenols Chemical class 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
OJMIONKXNSYLSR-UHFFFAOYSA-N phosphorous acid Chemical compound OP(O)O OJMIONKXNSYLSR-UHFFFAOYSA-N 0.000 description 1
239000000049 pigment Substances 0.000 description 1
239000006187 pill Substances 0.000 description 1
229920001643 poly(ether ketone) Polymers 0.000 description 1
229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 1
229920002492 poly(sulfone) Polymers 0.000 description 1
229920002401 polyacrylamide Polymers 0.000 description 1
229920000058 polyacrylate Polymers 0.000 description 1
229920002239 polyacrylonitrile Polymers 0.000 description 1
229920002647 polyamide Polymers 0.000 description 1
229920002857 polybutadiene Polymers 0.000 description 1
229920001748 polybutylene Polymers 0.000 description 1
229920006393 polyether sulfone Polymers 0.000 description 1
229920001195 polyisoprene Polymers 0.000 description 1
229920000193 polymethacrylate Polymers 0.000 description 1
229920006324 polyoxymethylene Polymers 0.000 description 1
235000013824 polyphenols Nutrition 0.000 description 1
229920001155 polypropylene Polymers 0.000 description 1
229920001451 polypropylene glycol Polymers 0.000 description 1
229920001296 polysiloxane Polymers 0.000 description 1
229920002223 polystyrene Polymers 0.000 description 1
239000011118 polyvinyl acetate Substances 0.000 description 1
229920002689 polyvinyl acetate Polymers 0.000 description 1
229920002451 polyvinyl alcohol Polymers 0.000 description 1
229920000915 polyvinyl chloride Polymers 0.000 description 1
239000004800 polyvinyl chloride Substances 0.000 description 1
229920002620 polyvinyl fluoride Polymers 0.000 description 1
229920002981 polyvinylidene fluoride Polymers 0.000 description 1
239000002243 precursor Substances 0.000 description 1
238000002360 preparation method Methods 0.000 description 1
125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
125000003548 sec-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
239000007787 solid Substances 0.000 description 1
239000000243 solution Substances 0.000 description 1
150000005846 sugar alcohols Polymers 0.000 description 1
239000000829 suppository 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
LVEOKSIILWWVEO-UHFFFAOYSA-N tetradecyl 3-(3-oxo-3-tetradecoxypropyl)sulfanylpropanoate Chemical compound CCCCCCCCCCCCCCOC(=O)CCSCCC(=O)OCCCCCCCCCCCCCC LVEOKSIILWWVEO-UHFFFAOYSA-N 0.000 description 1
CYRMSUTZVYGINF-UHFFFAOYSA-N trichlorofluoromethane Chemical compound FC(Cl)(Cl)Cl CYRMSUTZVYGINF-UHFFFAOYSA-N 0.000 description 1
WGKLOLBTFWFKOD-UHFFFAOYSA-N tris(2-nonylphenyl) phosphite Chemical compound CCCCCCCCCC1=CC=CC=C1OP(OC=1C(=CC=CC=1)CCCCCCCCC)OC1=CC=CC=C1CCCCCCCCC WGKLOLBTFWFKOD-UHFFFAOYSA-N 0.000 description 1
HBYRZSMDBQVSHO-UHFFFAOYSA-N tris(2-tert-butyl-4-methylphenyl) phosphite Chemical compound CC(C)(C)C1=CC(C)=CC=C1OP(OC=1C(=CC(C)=CC=1)C(C)(C)C)OC1=CC=C(C)C=C1C(C)(C)C HBYRZSMDBQVSHO-UHFFFAOYSA-N 0.000 description 1
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
235000019165 vitamin E Nutrition 0.000 description 1
229940046009 vitamin E Drugs 0.000 description 1
239000011709 vitamin E Substances 0.000 description 1
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1

Classifications

- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/81—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
- A61K8/8141—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
- A61K8/8152—Homopolymers or copolymers of esters, e.g. (meth)acrylic acid esters; Compositions of derivatives of such polymers
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q17/00—Barrier preparations; Preparations brought into direct contact with the skin for affording protection against external influences, e.g. sunlight, X-rays or other harmful rays, corrosive materials, bacteria or insect stings
- A61Q17/04—Topical preparations for affording protection against sunlight or other radiation; Topical sun tanning preparations
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/04—Oxygen-containing compounds
- C08K5/10—Esters; Ether-esters
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D7/00—Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
- C09D7/40—Additives
- C09D7/48—Stabilisers against degradation by oxygen, light or heat
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K15/00—Anti-oxidant compositions; Compositions inhibiting chemical change
- C09K15/04—Anti-oxidant compositions; Compositions inhibiting chemical change containing organic compounds
- C09K15/06—Anti-oxidant compositions; Compositions inhibiting chemical change containing organic compounds containing oxygen

Landscapes

Chemical & Material Sciences (AREA)
Health & Medical Sciences (AREA)
Life Sciences & Earth Sciences (AREA)
Organic Chemistry (AREA)
Animal Behavior & Ethology (AREA)
General Health & Medical Sciences (AREA)
Engineering & Computer Science (AREA)
Materials Engineering (AREA)
Veterinary Medicine (AREA)
Public Health (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Chemical Kinetics & Catalysis (AREA)
Birds (AREA)
Epidemiology (AREA)
Wood Science & Technology (AREA)
Dermatology (AREA)
Compositions Of Macromolecular Compounds (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Hydrogenated Pyridines (AREA)
Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Paints Or Removers (AREA)
Plural Heterocyclic Compounds (AREA)
Lubricants (AREA)
Laminated Bodies (AREA)

SK575-97A 1994-11-11 1995-11-03 Use of 3-arylacrylic acid esters as light-protection agents and stabilizers for non-living organic material SK57597A3 (en)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
DE4440288A DE4440288A1 (de)	1994-11-11	1994-11-11	Verwendung von 3-Arylacrylsäureestern als Lichtschutzmittel und Stabilisatoren für nicht lebendes organisches Material
PCT/EP1995/004313 WO1996015184A1 (de)	1994-11-11	1995-11-03	Verwendung von 3-arylacrylsäureestern als lichtschutzmittel und stabilisatoren für nicht lebendes organisches material

Publications (1)

Publication Number	Publication Date
SK57597A3 true SK57597A3 (en)	1998-06-03

Family

ID=6533049

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
SK575-97A SK57597A3 (en)	1994-11-11	1995-11-03	Use of 3-arylacrylic acid esters as light-protection agents and stabilizers for non-living organic material

Country Status (21)

Country	Link
US (1)	US5821292A (cs)
EP (1)	EP0791032B1 (cs)
JP (1)	JP3638607B2 (cs)
KR (1)	KR100421066B1 (cs)
CN (1)	CN1074010C (cs)
AT (1)	ATE192469T1 (cs)
AU (1)	AU3980495A (cs)
BG (1)	BG101484A (cs)
BR (1)	BR9509655A (cs)
CA (1)	CA2204916A1 (cs)
CZ (1)	CZ135097A3 (cs)
DE (2)	DE4440288A1 (cs)
ES (1)	ES2145935T3 (cs)
FI (1)	FI971992A0 (cs)
HU (1)	HUT76987A (cs)
NO (1)	NO972157L (cs)
PL (1)	PL320202A1 (cs)
PT (1)	PT791032E (cs)
SK (1)	SK57597A3 (cs)
TW (1)	TW399080B (cs)
WO (1)	WO1996015184A1 (cs)

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US6410620B2 (en)	1999-09-10	2002-06-25	General Electric Company	Color stable compositions containing arylate-comprising polymers
US6414058B2 (en)	1999-09-10	2002-07-02	General Electric Company	Color stable compositions containing arylate-comprising polymers
JP2003508616A (ja) *	1999-09-10	2003-03-04	ゼネラル・エレクトリック・カンパニイ	色安定性に優れたポリアリーレート含有組成物
DE19948117A1 (de)	1999-10-06	2001-04-12	Basf Ag	Stabilisatorzusammensetzung
DE10011317A1 (de) *	2000-03-10	2001-09-13	Basf Ag	Verwendung von aminosubstituierten Hydroxybenzophenonen als Lichtschutzmittel und Stabilisatoren für nicht lenbendes organisches Material
DE10120838A1 (de) *	2001-04-27	2002-10-31	Basf Ag	Stoffmischung zur UV-Stabilisierung von Kunststoffen und Herstellung davon
DE10161864A1 (de) *	2001-12-14	2003-07-03	Basf Ag	Stabilisatorzusammensetzung III
DE10161863A1 (de) *	2001-12-14	2003-07-03	Basf Ag	Stabilisatorzusammensetzung II
DE10161861A1 (de) *	2001-12-14	2003-07-03	Basf Ag	Stabilisatorzusammensetzung I
TWI329652B (en) *	2003-03-26	2010-09-01	Sumitomo Chemical Co	Resin composition and molded article thereof
JP4379174B2 (ja) *	2003-03-26	2009-12-09	住友化学株式会社	導光体
DE102004036965A1 (de) *	2004-07-30	2006-02-16	Basf Ag	Stabilisatorzusammensetzung aus flüssigen und festen UV-Absorbern
EP3309215B1 (en) *	2015-06-12	2019-07-24	Mitsubishi Chemical Corporation	Resin composition, film using same and multilayer structure
CN108473742B (zh) *	2015-12-16	2021-11-12	三菱化学株式会社	树脂组合物及使用其的熔融成型品、以及多层结构体
CN109843963B (zh) *	2016-10-14	2022-05-13	旭化成株式会社	异氰酸酯组合物、异氰酸酯聚合物的制造方法和异氰酸酯聚合物
CN109306133B (zh) *	2018-08-13	2020-11-17	内蒙古科技大学	Pvc用咪唑羧酸稀土复合热稳定剂及其制备方法

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US2775574A (en) *	1953-04-27	1956-12-25	Monsanto Chemicals	Acrylonitrile copolymers stabilized with cinnamic acid and its salts
US3074971A (en) *	1959-01-23	1963-01-22	Gen Aniline & Film Corp	alpha-cyanocinnamic acid esters
US3052636A (en) *	1959-05-26	1962-09-04	Gen Aniline & Film Corp	Ultra-violet light stabilized organic compositions
US3085097A (en) *	1960-03-09	1963-04-09	Gen Aniline & Film Corp	alpha-cyano, 2-alkoxy-1-naphthaleneacrylic acid esters
US3278448A (en) *	1960-05-17	1966-10-11	Bayer Ag	Ultra-violet protective light filter
US3244668A (en) *	1961-01-23	1966-04-05	Ethyl Corp	Stabilized plastic
DE1694137B2 (de) *	1967-03-09	1975-09-04	Bayer Ag, 5090 Leverkusen	Formteile aus Polycarbonaten mit veredelten Oberflächen und Verfahren zu deren Herstellung
DE1922815A1 (de) *	1969-05-05	1970-11-12	Merck Anlagen Gmbh	Phenolaether und Phenolester als Stabilisatoren
US4273833A (en) *	1975-09-19	1981-06-16	United States Trading International, Inc.	Anti-fouling overcoating composition and use thereof
US4049869A (en) *	1975-09-19	1977-09-20	United States Trading International, Inc.	Method for preserving porous inorganic substrates
JPS53102357A (en) *	1977-02-17	1978-09-06	Adeka Argus Chem Co Ltd	Stabilized halogen-containing resin compsition
JPS5935941B2 (ja) *	1979-04-02	1984-08-31	株式会社資生堂	紫外線吸収剤
US5000945A (en) *	1986-04-22	1991-03-19	Ajinomoto Co., Inc.	Method of stabilizing a UVB absorbing compound, a stabilized UV absorber, and a cosmetic composition containing the same
JPH06104647B2 (ja) *	1992-01-29	1994-12-21	和歌山県	フェルラ酸誘導体、その製造方法および紫外線吸収剤
JPH07207063A (ja) *	1994-01-11	1995-08-08	Toppan Printing Co Ltd	耐光性プラスチック組成物
DE4405670A1 (de) *	1994-02-23	1995-08-24	Basf Ag	Stabilisatorgemisch aus Chromanderivaten, organischen Phosphiten oder Phosphoniten und Aminen

1994
- 1994-11-11 DE DE4440288A patent/DE4440288A1/de not_active Withdrawn
1995
- 1995-11-03 JP JP51568896A patent/JP3638607B2/ja not_active Expired - Fee Related
- 1995-11-03 BR BR9509655A patent/BR9509655A/pt not_active IP Right Cessation
- 1995-11-03 CN CN95196614A patent/CN1074010C/zh not_active Expired - Fee Related
- 1995-11-03 WO PCT/EP1995/004313 patent/WO1996015184A1/de not_active Ceased
- 1995-11-03 HU HU9701801A patent/HUT76987A/hu unknown
- 1995-11-03 SK SK575-97A patent/SK57597A3/sk unknown
- 1995-11-03 EP EP95938396A patent/EP0791032B1/de not_active Expired - Lifetime
- 1995-11-03 KR KR1019970703118A patent/KR100421066B1/ko not_active Expired - Fee Related
- 1995-11-03 AU AU39804/95A patent/AU3980495A/en not_active Abandoned
- 1995-11-03 ES ES95938396T patent/ES2145935T3/es not_active Expired - Lifetime
- 1995-11-03 CZ CZ971350A patent/CZ135097A3/cs unknown
- 1995-11-03 US US08/836,043 patent/US5821292A/en not_active Expired - Lifetime
- 1995-11-03 PL PL95320202A patent/PL320202A1/xx unknown
- 1995-11-03 DE DE59508283T patent/DE59508283D1/de not_active Expired - Lifetime
- 1995-11-03 PT PT95938396T patent/PT791032E/pt unknown
- 1995-11-03 CA CA002204916A patent/CA2204916A1/en not_active Abandoned
- 1995-11-03 AT AT95938396T patent/ATE192469T1/de not_active IP Right Cessation
- 1995-11-03 FI FI971992A patent/FI971992A0/fi not_active Application Discontinuation
- 1995-11-09 TW TW084111860A patent/TW399080B/zh active
1997
- 1997-05-09 NO NO972157A patent/NO972157L/no unknown
- 1997-05-14 BG BG101484A patent/BG101484A/xx unknown

Also Published As

Publication number	Publication date
BG101484A (bg)	1997-10-31
FI971992A7 (fi)	1997-05-09
BR9509655A (pt)	1997-10-14
NO972157L (no)	1997-05-12
TW399080B (en)	2000-07-21
KR100421066B1 (ko)	2004-06-30
AU3980495A (en)	1996-06-06
CA2204916A1 (en)	1996-05-23
WO1996015184A1 (de)	1996-05-23
KR970707220A (ko)	1997-12-01
FI971992L (fi)	1997-05-09
EP0791032A1 (de)	1997-08-27
NO972157D0 (no)	1997-05-09
JP3638607B2 (ja)	2005-04-13
DE4440288A1 (de)	1996-05-15
PL320202A1 (en)	1997-09-15
MX9703407A (es)	1997-07-31
HUT76987A (hu)	1998-01-28
EP0791032B1 (de)	2000-05-03
US5821292A (en)	1998-10-13
CN1168683A (zh)	1997-12-24
JPH10508642A (ja)	1998-08-25
FI971992A0 (fi)	1997-05-09
ATE192469T1 (de)	2000-05-15
CZ135097A3 (cs)	1998-04-15
PT791032E (pt)	2000-10-31
ES2145935T3 (es)	2000-07-16
DE59508283D1 (de)	2000-06-08
CN1074010C (zh)	2001-10-31

Publication	Publication Date	Title
US5821292A (en)	1998-10-13	3-arylacrylic acid ester light-protection stabilizers for organic material
MXPA97003351A (es)	1997-08-01	Esteres 2-cianoacrilicos
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