KR100457006B1 - 안정화제혼합물 - Google Patents
안정화제혼합물 Download PDFInfo
- Publication number
- KR100457006B1 KR100457006B1 KR1019970046267A KR19970046267A KR100457006B1 KR 100457006 B1 KR100457006 B1 KR 100457006B1 KR 1019970046267 A KR1019970046267 A KR 1019970046267A KR 19970046267 A KR19970046267 A KR 19970046267A KR 100457006 B1 KR100457006 B1 KR 100457006B1
- Authority
- KR
- South Korea
- Prior art keywords
- alkyl
- substituted
- cycloalkyl
- alkoxy
- formula
- 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.)
- Expired - Lifetime
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 130
- 239000003381 stabilizer Substances 0.000 title claims description 35
- 150000001875 compounds Chemical class 0.000 claims abstract description 108
- 239000003973 paint Substances 0.000 claims abstract description 63
- 239000011368 organic material Substances 0.000 claims abstract description 13
- 239000000463 material Substances 0.000 claims abstract description 11
- 230000000087 stabilizing effect Effects 0.000 claims abstract description 8
- 125000000217 alkyl group Chemical group 0.000 claims description 262
- -1 = O Chemical group 0.000 claims description 252
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 102
- 229910052739 hydrogen Inorganic materials 0.000 claims description 92
- XTFIVUDBNACUBN-UHFFFAOYSA-N 1,3,5-trinitro-1,3,5-triazinane Chemical compound [O-][N+](=O)N1CN([N+]([O-])=O)CN([N+]([O-])=O)C1 XTFIVUDBNACUBN-UHFFFAOYSA-N 0.000 claims description 83
- 239000001257 hydrogen Substances 0.000 claims description 79
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 56
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 55
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 45
- 125000004430 oxygen atom Chemical group O* 0.000 claims description 45
- 125000002947 alkylene group Chemical group 0.000 claims description 43
- 125000003545 alkoxy group Chemical group 0.000 claims description 42
- 125000003118 aryl group Chemical group 0.000 claims description 40
- 125000000000 cycloalkoxy group Chemical group 0.000 claims description 35
- 125000003342 alkenyl group Chemical group 0.000 claims description 32
- 229910052736 halogen Inorganic materials 0.000 claims description 29
- 125000003884 phenylalkyl group Chemical group 0.000 claims description 29
- 150000002367 halogens Chemical class 0.000 claims description 28
- 229910052799 carbon Inorganic materials 0.000 claims description 27
- 229910052760 oxygen Inorganic materials 0.000 claims description 27
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 26
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims description 24
- 125000003860 C1-C20 alkoxy group Chemical group 0.000 claims description 24
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims description 24
- 125000003358 C2-C20 alkenyl group Chemical group 0.000 claims description 19
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 19
- 150000001412 amines Chemical class 0.000 claims description 18
- 239000001301 oxygen Substances 0.000 claims description 18
- 125000004423 acyloxy group Chemical group 0.000 claims description 17
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 17
- 239000011230 binding agent Substances 0.000 claims description 17
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims description 17
- 150000002431 hydrogen Chemical class 0.000 claims description 15
- 125000005037 alkyl phenyl group Chemical group 0.000 claims description 13
- 125000004642 (C1-C12) alkoxy group Chemical group 0.000 claims description 12
- 125000000304 alkynyl group Chemical group 0.000 claims description 12
- 239000000126 substance Substances 0.000 claims description 12
- 229920001169 thermoplastic Polymers 0.000 claims description 12
- 125000004442 acylamino group Chemical group 0.000 claims description 11
- 125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 claims description 11
- 125000005843 halogen group Chemical group 0.000 claims description 11
- 125000001931 aliphatic group Chemical group 0.000 claims description 10
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 10
- 239000004611 light stabiliser Substances 0.000 claims description 10
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 claims description 9
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 claims description 8
- 125000003944 tolyl group Chemical group 0.000 claims description 8
- 125000001589 carboacyl group Chemical group 0.000 claims description 7
- 229910052801 chlorine Inorganic materials 0.000 claims description 7
- 125000000392 cycloalkenyl group Chemical group 0.000 claims description 7
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 6
- 150000001721 carbon Chemical group 0.000 claims description 6
- 125000002933 cyclohexyloxy group Chemical group C1(CCCCC1)O* 0.000 claims description 6
- NIHNNTQXNPWCJQ-UHFFFAOYSA-N fluorene Chemical compound C1=CC=C2CC3=CC=CC=C3C2=C1 NIHNNTQXNPWCJQ-UHFFFAOYSA-N 0.000 claims description 6
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims description 5
- 125000001624 naphthyl group Chemical group 0.000 claims description 5
- 125000002071 phenylalkoxy group Chemical group 0.000 claims description 5
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 claims description 4
- FJGQBLRYBUAASW-UHFFFAOYSA-N 2-(benzotriazol-2-yl)phenol Chemical compound OC1=CC=CC=C1N1N=C2C=CC=CC2=N1 FJGQBLRYBUAASW-UHFFFAOYSA-N 0.000 claims description 4
- CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical compound [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 claims description 4
- 229910052783 alkali metal Inorganic materials 0.000 claims description 4
- 150000001340 alkali metals Chemical class 0.000 claims description 4
- 125000004450 alkenylene group Chemical group 0.000 claims description 4
- 125000004429 atom Chemical group 0.000 claims description 4
- 125000004985 dialkyl amino alkyl group Chemical group 0.000 claims description 4
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 4
- 125000006839 xylylene group Chemical group 0.000 claims description 4
- 125000004648 C2-C8 alkenyl group Chemical group 0.000 claims description 3
- 125000003302 alkenyloxy group Chemical group 0.000 claims description 3
- 125000004183 alkoxy alkyl group Chemical group 0.000 claims description 3
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims description 3
- 125000003282 alkyl amino group Chemical group 0.000 claims description 3
- 125000005336 allyloxy group Chemical group 0.000 claims description 3
- 125000002490 anilino group Chemical group [H]N(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims description 3
- 125000000732 arylene group Chemical group 0.000 claims description 3
- 125000002529 biphenylenyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3C12)* 0.000 claims description 3
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims description 3
- 125000006297 carbonyl amino group Chemical group [H]N([*:2])C([*:1])=O 0.000 claims description 3
- 235000013601 eggs Nutrition 0.000 claims description 3
- 125000002757 morpholinyl group Chemical group 0.000 claims description 3
- 125000005184 naphthylamino group Chemical group C1(=CC=CC2=CC=CC=C12)N* 0.000 claims description 3
- 125000004193 piperazinyl group Chemical group 0.000 claims description 3
- 125000003386 piperidinyl group Chemical group 0.000 claims description 3
- SNOOUWRIMMFWNE-UHFFFAOYSA-M sodium;6-[(3,4,5-trimethoxybenzoyl)amino]hexanoate Chemical compound [Na+].COC1=CC(C(=O)NCCCCCC([O-])=O)=CC(OC)=C1OC SNOOUWRIMMFWNE-UHFFFAOYSA-M 0.000 claims description 3
- 125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 claims description 3
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 49
- 229920001577 copolymer Polymers 0.000 description 36
- 229920000642 polymer Polymers 0.000 description 36
- 150000003254 radicals Chemical class 0.000 description 36
- 229910052757 nitrogen Inorganic materials 0.000 description 35
- 239000011347 resin Substances 0.000 description 23
- 229920005989 resin Polymers 0.000 description 23
- 229920002647 polyamide Polymers 0.000 description 21
- 239000004952 Polyamide Substances 0.000 description 20
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 19
- 229910052751 metal Inorganic materials 0.000 description 17
- 239000002184 metal Substances 0.000 description 17
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 15
- 239000004417 polycarbonate Substances 0.000 description 15
- 239000003054 catalyst Substances 0.000 description 14
- 150000002148 esters Chemical class 0.000 description 14
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 13
- 229920000728 polyester Polymers 0.000 description 13
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 12
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 12
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 12
- 229920006324 polyoxymethylene Polymers 0.000 description 12
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 11
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 11
- 239000004721 Polyphenylene oxide Substances 0.000 description 11
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 11
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 10
- 239000005977 Ethylene Substances 0.000 description 10
- 239000004743 Polypropylene Substances 0.000 description 10
- 229920001971 elastomer Polymers 0.000 description 10
- 238000000034 method Methods 0.000 description 10
- 239000004814 polyurethane Substances 0.000 description 10
- 229920000877 Melamine resin Polymers 0.000 description 9
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 9
- 239000008199 coating composition Substances 0.000 description 9
- 229920002857 polybutadiene Polymers 0.000 description 9
- 229920000515 polycarbonate Polymers 0.000 description 9
- 239000005062 Polybutadiene Substances 0.000 description 8
- 229920000122 acrylonitrile butadiene styrene Polymers 0.000 description 8
- KBPLFHHGFOOTCA-UHFFFAOYSA-N caprylic alcohol Natural products CCCCCCCCO KBPLFHHGFOOTCA-UHFFFAOYSA-N 0.000 description 8
- 229920001684 low density polyethylene Polymers 0.000 description 8
- 239000004702 low-density polyethylene Substances 0.000 description 8
- GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 description 8
- 229920000570 polyether Polymers 0.000 description 8
- 229920006380 polyphenylene oxide Polymers 0.000 description 8
- 229920002635 polyurethane Polymers 0.000 description 8
- 239000000843 powder Substances 0.000 description 8
- 239000000047 product Substances 0.000 description 8
- 239000000243 solution Substances 0.000 description 8
- 239000007859 condensation product Substances 0.000 description 7
- 239000004700 high-density polyethylene Substances 0.000 description 7
- 239000007787 solid Substances 0.000 description 7
- 229920002554 vinyl polymer Polymers 0.000 description 7
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 6
- 239000004698 Polyethylene Substances 0.000 description 6
- 239000002253 acid Substances 0.000 description 6
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 6
- 125000004432 carbon atom Chemical group C* 0.000 description 6
- 239000003795 chemical substances by application Substances 0.000 description 6
- 150000001993 dienes Chemical class 0.000 description 6
- 239000000806 elastomer Substances 0.000 description 6
- NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 description 6
- 229920001903 high density polyethylene Polymers 0.000 description 6
- 238000002844 melting Methods 0.000 description 6
- 230000008018 melting Effects 0.000 description 6
- 150000002739 metals Chemical class 0.000 description 6
- 238000002156 mixing Methods 0.000 description 6
- 229920000058 polyacrylate Polymers 0.000 description 6
- 229920000573 polyethylene Polymers 0.000 description 6
- 229920001228 polyisocyanate Polymers 0.000 description 6
- 239000005056 polyisocyanate Substances 0.000 description 6
- 229920000098 polyolefin Polymers 0.000 description 6
- 229920001155 polypropylene Polymers 0.000 description 6
- 239000004800 polyvinyl chloride Substances 0.000 description 6
- 229920000915 polyvinyl chloride Polymers 0.000 description 6
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 6
- ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 description 5
- 0 CC(C)(*)Oc(cc1O)c(*)cc1-c1nc(-c(cc2)ccc2-c2ccccc2)nc(-c(cc2)ccc2-c2ccccc2)n1 Chemical compound CC(C)(*)Oc(cc1O)c(*)cc1-c1nc(-c(cc2)ccc2-c2ccccc2)nc(-c(cc2)ccc2-c2ccccc2)n1 0.000 description 5
- 229920001400 block copolymer Polymers 0.000 description 5
- 238000000576 coating method Methods 0.000 description 5
- 125000005842 heteroatom Chemical group 0.000 description 5
- 239000012948 isocyanate Substances 0.000 description 5
- 239000000049 pigment Substances 0.000 description 5
- 229920001707 polybutylene terephthalate Polymers 0.000 description 5
- 229920000647 polyepoxide Polymers 0.000 description 5
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 5
- 230000005855 radiation Effects 0.000 description 5
- 239000000758 substrate Substances 0.000 description 5
- 150000005846 sugar alcohols Polymers 0.000 description 5
- 239000004416 thermosoftening plastic Substances 0.000 description 5
- KAKZBPTYRLMSJV-UHFFFAOYSA-N vinyl-ethylene Natural products C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 5
- DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 description 4
- BPXVHIRIPLPOPT-UHFFFAOYSA-N 1,3,5-tris(2-hydroxyethyl)-1,3,5-triazinane-2,4,6-trione Chemical compound OCCN1C(=O)N(CCO)C(=O)N(CCO)C1=O BPXVHIRIPLPOPT-UHFFFAOYSA-N 0.000 description 4
- ALVZNPYWJMLXKV-UHFFFAOYSA-N 1,9-Nonanediol Chemical compound OCCCCCCCCCO ALVZNPYWJMLXKV-UHFFFAOYSA-N 0.000 description 4
- ZPIRWAHWDCHWLM-UHFFFAOYSA-N 2-dodecylsulfanylethanol Chemical compound CCCCCCCCCCCCSCCO ZPIRWAHWDCHWLM-UHFFFAOYSA-N 0.000 description 4
- CKPKHTKLLYPGFM-UHFFFAOYSA-N 6,6-dimethylheptane-1,1-diol Chemical compound CC(CCCCC(O)O)(C)C CKPKHTKLLYPGFM-UHFFFAOYSA-N 0.000 description 4
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 4
- 229920002943 EPDM rubber Polymers 0.000 description 4
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 4
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 4
- 229920002292 Nylon 6 Polymers 0.000 description 4
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 4
- 229930040373 Paraformaldehyde Natural products 0.000 description 4
- 229920002396 Polyurea Polymers 0.000 description 4
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 4
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 4
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 4
- 229920000180 alkyd Polymers 0.000 description 4
- 150000008064 anhydrides Chemical class 0.000 description 4
- 239000003963 antioxidant agent Substances 0.000 description 4
- 235000006708 antioxidants Nutrition 0.000 description 4
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 4
- MTAZNLWOLGHBHU-UHFFFAOYSA-N butadiene-styrene rubber Chemical compound C=CC=C.C=CC1=CC=CC=C1 MTAZNLWOLGHBHU-UHFFFAOYSA-N 0.000 description 4
- 239000011248 coating agent Substances 0.000 description 4
- 150000001991 dicarboxylic acids Chemical class 0.000 description 4
- XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 description 4
- 229920000554 ionomer Polymers 0.000 description 4
- ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 description 4
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 4
- DNIAPMSPPWPWGF-UHFFFAOYSA-N monopropylene glycol Natural products CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 4
- FPQJEXTVQZHURJ-UHFFFAOYSA-N n,n'-bis(2-hydroxyethyl)oxamide Chemical compound OCCNC(=O)C(=O)NCCO FPQJEXTVQZHURJ-UHFFFAOYSA-N 0.000 description 4
- TVMXDCGIABBOFY-UHFFFAOYSA-N n-Octanol Natural products CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 4
- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 4
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 4
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 4
- 238000006116 polymerization reaction Methods 0.000 description 4
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 4
- 238000002360 preparation method Methods 0.000 description 4
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 4
- 235000013772 propylene glycol Nutrition 0.000 description 4
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 4
- 239000005060 rubber Substances 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- 229910052717 sulfur Inorganic materials 0.000 description 4
- YODZTKMDCQEPHD-UHFFFAOYSA-N thiodiglycol Chemical compound OCCSCCO YODZTKMDCQEPHD-UHFFFAOYSA-N 0.000 description 4
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 4
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- JYEUMXHLPRZUAT-UHFFFAOYSA-N 1,2,3-triazine Chemical group C1=CN=NN=C1 JYEUMXHLPRZUAT-UHFFFAOYSA-N 0.000 description 3
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 3
- RMSGQZDGSZOJMU-UHFFFAOYSA-N 1-butyl-2-phenylbenzene Chemical group CCCCC1=CC=CC=C1C1=CC=CC=C1 RMSGQZDGSZOJMU-UHFFFAOYSA-N 0.000 description 3
- ONTODYXHFBKCDK-UHFFFAOYSA-N 2-(2,4-dimethylphenyl)-1,3,5-triazine Chemical compound CC1=CC(C)=CC=C1C1=NC=NC=N1 ONTODYXHFBKCDK-UHFFFAOYSA-N 0.000 description 3
- IUVCFHHAEHNCFT-INIZCTEOSA-N 2-[(1s)-1-[4-amino-3-(3-fluoro-4-propan-2-yloxyphenyl)pyrazolo[3,4-d]pyrimidin-1-yl]ethyl]-6-fluoro-3-(3-fluorophenyl)chromen-4-one Chemical compound C1=C(F)C(OC(C)C)=CC=C1C(C1=C(N)N=CN=C11)=NN1[C@@H](C)C1=C(C=2C=C(F)C=CC=2)C(=O)C2=CC(F)=CC=C2O1 IUVCFHHAEHNCFT-INIZCTEOSA-N 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- 229940126062 Compound A Drugs 0.000 description 3
- 229920000089 Cyclic olefin copolymer Polymers 0.000 description 3
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical group C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 3
- 239000004716 Ethylene/acrylic acid copolymer Substances 0.000 description 3
- 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 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- SJRJJKPEHAURKC-UHFFFAOYSA-N N-Methylmorpholine Chemical compound CN1CCOCC1 SJRJJKPEHAURKC-UHFFFAOYSA-N 0.000 description 3
- 239000004734 Polyphenylene sulfide Substances 0.000 description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- 239000007983 Tris buffer Substances 0.000 description 3
- 239000006096 absorbing agent Substances 0.000 description 3
- 239000000654 additive Substances 0.000 description 3
- 239000001361 adipic acid Substances 0.000 description 3
- 235000011037 adipic acid Nutrition 0.000 description 3
- 230000032683 aging Effects 0.000 description 3
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 3
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- 239000004711 α-olefin Substances 0.000 description 1
- QUEDXNHFTDJVIY-UHFFFAOYSA-N γ-tocopherol Chemical class OC1=C(C)C(C)=C2OC(CCCC(C)CCCC(C)CCCC(C)C)(C)CCC2=C1 QUEDXNHFTDJVIY-UHFFFAOYSA-N 0.000 description 1
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Abstract
Description
Claims (9)
- 하기 화학식(1)의 화합물 및 화학식(2)의 화합물을 포함하는 혼합물:화학식 (1)중에서,G1은 수소 또는 -OG이고;k는 1 또는 2이며; 또 k=1이면,G는 수소 또는 C1-C18알킬이거나; 또는 OH, C1-C18알콕시, C5-C12시클로알콕시, 알릴옥시, 할로겐, =O, -COOH, -COOG8, -CONH2, -CONHG9, -CON(G9)(G10), -NH2, -NHG9, =NG9, -N(G9)(G10), -NHCOG11, -CN, -OCOG11, 페녹시 및/또는 C1-C18알킬-, C1-C18알콕시- 또는 할로-치환된 페녹시에 의해 치환된 C1-C18알킬이거나; 또는 G는 중간에 -O-를 포함하고 또 OH에 의해 치환될 수 있는 C3-C50알킬이거나; 또는 G는 C3-C6알케닐; 글리시딜; C5-C12시클로알킬; OH, C1-C4알킬 또는 -OCOG11에 의해 치환된 C5-C12시클로알킬; 비치환되거나 또는 OH, Cl, C1-C18알콕시 또는 C1-C18알킬에 의해 치환된 C7-C11페닐알킬; -CO-G12 또는 -SO2-G13이고;G3, G4 및 G5는 서로 독립해서 H, C1-C12알킬; C2-C6알케닐; C1-C18알콕시; C5-C12시클로알콕시; C2-C18알케녹시; 할로겐; -C≡ N; C1-C4할로알킬; C7-C11페닐알킬; COOG8; CONH2; CONHG9; CONG9G10; 술포; C2-C18아실아미노; OCOG11; 페닐옥시; 또는 C1-C18알킬, C1-C18알콕시 또는 할로겐에 의해 치환된 페닐옥시, C1-C12알킬 또는 C1-C18알콕시이고; 또 화학식 (1)중의 한 개 라디칼 G3은 부가적으로 -NG16G17의 의미를 가지며;G6은 화학식(2)에서 R1에 지시한 의미를 포함하고;G8은 C1-C18알킬; C3-C18알케닐; 중간에 O, NH, NG9 또는 S를 포함하고 및/또는 OH에 의해 치환된 C3-C50알킬; -P(O)(OG14)2, -N(G9)(G10) 또는 -OCOG11 및/또는 OH에 의해 치환된 C1-C4알킬; 글리시딜; C5-C12시클로알킬; C1-C4알킬시클로헥실; 페닐; C7-C14알킬페닐; C6-C15비시클로알킬; C6-C15비시클로알케닐; C6-C15트리시클로알킬; C6-C15비시클로알킬; 또는 C7-C11페닐알킬이며;G9 및 G10은 서로 독립해서 C1-C12알킬; C3-C12알콕시알킬; C2-C18알카노일; C4-C16디알킬아미노알킬 또는 C5-C12시클로알킬이거나; 또는G9 및 G10은 합쳐져서 C3-C9알킬렌 또는 -옥사알킬렌 또는 -아자알킬렌이며;G11은 C1-C18알킬; C1-C12알콕시; C2-C18알케닐; C7-C11페닐알킬; C7-C11페닐알콕시; C6-C12시클로알킬; C6-C12시클로알콕시; 페녹시 또는 페닐이거나; 또는 중간에 -O-를 포함하고 또 OH에 의해 치환될 수 있는 C3-C50알킬이고;G12는 C1-C18알킬; C2-C18알케닐; 페닐; C1-C18알콕시; C3-C18알케닐옥시; 중간에 O, NH, NG9 또는 S를 포함하고 및/또는 OH에 의해 치환된 C3-C50알콕시; 시클로헥실옥시; 페녹시; C7-C14알킬페녹시; C7-C11페닐알콕시; C1-C12알킬아미노; 페닐아미노; 톨릴아미노 또는 나프틸아미노이며;G13은 C1-C12알킬; 페닐; 나프틸 또는 C7-C14알킬페닐이고;G14는 C1-C12알킬, 메틸페닐 또는 페닐이며;G16은 수소 또는 C1-C20알킬이고;G17은 수소, C1-C20알킬, C7-C13페닐알킬, -C(=O)-G19, -C(=O)-NH-G16이며; 또G19는 C1-C20알킬; 중간에 1 내지 6개의 산소 원자를 갖고 및/또는 OH, 할로겐, NH2, NHG9 또는 NG9G10에 의해 치환된 C2-C20알킬; 페닐; C7-C13페닐알킬 또는 C2-C20알케닐이고;또 k=2 이면,E1 및 E2는 화학식(1a)의 기이고;G는 C2-C16알킬렌, C4-C12알케닐렌, 크실릴렌, 중간에 -O-를 포함하고 및/또는 OH에 의해 치환될 수 있는 C3-C20알킬렌이거나, 또는 화학식 -CH2CH(OH)CH2O-G20-OCH2CH(OH)CH2-, -CO-G21-CO-, -CO-NH-G22-NH-CO-, -(CH2)j-COO-G20-OOC-(CH2)j- (이때, j는 1 내지 3 범위의 수임)이거나, 또는G20은 C2-C10알킬렌; 중간에 O, 페닐렌 또는 -페닐렌-E-페닐렌-을 포함하는 C4-C50알킬렌이고, E는 -O-, -S-, -SO2-, -CH2-, -CO- 또는 -C(CH3)2- 이며,G21은 C2-C10알킬렌, C2-C10옥사알킬렌, C2-C10티아알킬렌, C6-C12아릴렌 또는 C2-C6알케닐렌이고;또 화학식(2)에서,R1은 수소; C1-C24알킬 또는 C5-C12시클로알킬이거나; 또는 1 내지 9개의 할로겐 원자, -R4, -OR5, -N(R5)2, =NR5, =O, -CON(R5)2, -COR5, -COOR5, -OCOR5, -OCON(R5)2, -CN, -NO2, -SR5, -SO2R5, -P(O)(OR5)2, 모르폴리닐, 피페리디닐, 2,2,6,6-테트라메틸피페리디닐, 피페라지닐 또는 N-메틸피페라지닐 기 또는 이들의 조합에 의해 치환된 C1-C24알킬 또는 C5-C12시클로알킬이거나; 또는 중간에 1 내지 6개의 페닐렌, -O-, -NR5-, -CONR5-, -COO-, -OCO-, -CH(R5)-, -C(R5)2- 또는 -CO- 기 또는 이들의 조합을 포함하는 C5-C12시클로알킬 또는 C1-C24알킬이거나; 또는 R1은 C2-C24알케닐; 할로겐; -SR3, SOR3; SO2R3; -SO3H; 또는 SO3M 이며;R3은 C1-C20알킬; C3-C18알케닐; C5-C12시클로알킬; C7-C15페닐알킬, 또는 비치환되거나 또는 1 내지 3개의 C1-C4알킬에 의해 치환된 C6-C12아릴이고;R4는 비치환된 C6-C12아릴; 또는 1 내지 3개의 할로겐 원자, C1-C8알킬 또는 C1-C8알콕시 또는 이들의 조합에 의해 치환된 C6-C12아릴; C5-C12시클로알킬; 비치환된 C7-C15페닐알킬이거나; 또는 페닐 고리에서 1 내지 3개의 할로겐 원자, C1-C8알킬, C1-C8알콕시 또는 이들의 조합에 의해 치환된 C7-C15페닐알킬이거나; 또는 C2-C8알케닐이며;R5는 R4; 수소; C1-C24알킬; 또는 화학식(1c) 의 라디칼이고, T는 수소; C1-C8알킬; 히드록시 기 또는 아실옥시 기에 의해 치환된 C2-C8알킬; 옥실; 히드록시; -CH2CN; C1-C18알콕시; C5-C12시클로알콕시; C3-C6알케닐; C7-C9페닐알킬; 페닐 고리에서 C1-C4알킬에 의해 1회, 2회 또는 3회 치환된 C7-C9페닐알킬이거나; 또는 지방족 C1-C8알카노일이며;R6 내지 R15는 서로 독립해서 수소; 히드록시; -C≡N; C1-C20알킬; C1-C20알콕시; C7-C20페닐알킬; C4-C12시클로알킬; C4-C12시클로알콕시; 할로겐; 할로-C1-C5알킬; 술포닐; 카르복시; 아실아미노; 아실옥시; C1-C12알콕시카르보닐; 아미노카르보닐; -O-Y; 또는 -O-Z이거나; 또는 R8 및 R9는 페닐 라디칼과 합쳐져서 중간에 하나 이상의 산소 또는 질소 원자를 포함하는 고리상 라디칼이고; 또 R11은 q가 0이면, 부가적으로 -NG16G17의 의미를 포함하고, G16 및 G17은 상기 정의된 의미를 가지며;M은 알칼리 금속이고;p는 1 또는 2이며;q는 0 또는 1이고;p=1 이면,X, Y 및 Z는 서로 독립해서 Ry; Rx에 의해 치환된 C1-C24알킬; 중간에 산소 원자를 포함하고 RX에 의해 치환된 C2-C50알킬; -Rx에 의해 치환된 C4-C12시클로알킬; -ORy에 의해 치환된 C4-C12시클로알킬; 중간에 산소 원자를 포함하는 C4-C20알케닐이거나; 또는 화학식R2 및 R'2는 서로 독립해서, 탄소원자에 부착된 경우, Rx이고; 또 탄소 이외의 원자에 부착된 경우, Ry이며;n은 0 내지 20이고; 또m은 0 내지 20이며; 또p=2 이면,Y 및 Z는 서로 독립해서 p=1일 때와 동일한 의미를 가지며; 또X는 C2-C12알킬렌; -CO-(C2-C12알킬렌)-CO-; -CO-페닐렌-CO-; CO-비페닐렌-CO-; CO-O-(C2-C12알킬렌)-O-CO-; -CO-O-페닐렌-O-CO; -CO-O-비페닐렌-O-CO-; -CO-NR'-(C2-C12알킬렌)-NR'-CO-; -CO-NR'-페닐렌-NR'-CO; -CO-NR'-비페닐렌-NR'-CO-; -CH2-CH(OH)-CH2-; -CH2-CH(OR2)-CH2-; -CH2-CH(OH)-CH2-O-D-O-CH2-CH(OH)-CH2; -CH((CH2)nR2)-COO-D-OOC-CH((CH2)nR2)-; -CH2-CH(OR2)-CH2-O-D-O-CH2-CH(OR2)-CH2- 이고;D는 C2-C12알킬렌; 중간에 산소 원자를 포함하는 C4-C50알킬렌; 페닐렌; 비페닐렌 또는 페닐렌-E-페닐렌이며;E는 -O-; -S-; -SO2-; -CH2-; -CO-; 또는 -C(CH3)2- 이고;Rx는 수소; 히드록시; C1-C20알킬; C4-C12시클로알킬; C1-C20알콕시; C4-C12시클로알콕시; 중간에 산소 원자를 포함하는 C4-C12시클로알킬 또는 C4-C12시클로알콕시; C6-C12아릴; 헤테로-C3-C12아릴; -ORz; NHRz; Rz; CONR'R"; 알릴; C2-C20알케닐; C4-C12시클로알케닐; 중간에 산소 원자를 포함하는 C4-C12시클로알케닐; C3-C20알키닐; 또는 C6-C12시클로알키닐; 또는 히드록시, -NH2, -NH-C1-C8알킬, -NH-시클로헥실, -N(C1-C8알킬)2, 디시클로헥실아미노, 할로겐, C1-C20알킬, C1-C20알콕시, C4-C12시클로알킬, C4-C12시클로알콕시, C2-C20알케닐, C4-C12시클로알킬, C3-C20알키닐, C6-C12시클로알키닐, C6-C12아릴, 아실아미노, 아실옥시, 술포닐, 카르복시, (메트)아크릴옥시, (메트)아크릴아미노, 에 의해 치환된 C1-C20알킬, C2-C20알콕시 또는 C4-C12시클로알킬이며;Ry는 수소; C1-C20알킬; C4-C12시클로알킬; 중간에 산소 원자를 포함하는 C4-C12시클로알킬; C6-C12아릴; 헤테로-C3-C12아릴; -Rz; 알릴; C2-C20알케닐; 중간에 산소 원자를 포함하거나 포함하지 않는 C4-C12시클로알케닐; C3-C20알키닐; 또는 C6-C12시클로알키닐; 또는 히드록시, -NH2, -NH-C1-C8알킬, -NH-시클로헥실, -N(C1-C8알킬)2, 디시클로헥실아미노, 할로겐, C1-C20알킬, C1-C20알콕시, C4-C12시클로알킬, C4-C12시클로알콕시, C2-C20알케닐, C4-C12시클로알킬, C3-C20알키닐, C6-C12시클로알키닐, C6-C12아릴, 아실아민, 아실옥시, 술포닐, 카르복시, (메트)아크릴옥시, (메트)아크릴아미노, 에 의해 치환된 C1-C20알킬 또는 C4-C12시클로알킬이고;Rz는 -COR'; -COOR'; -CONR'R"; -CO-CH=CH2; -CO-C(CH3)=CH2 이며;R' 및 R"는 서로 독립해서 수소; C1-C20알킬; 중간에 산소 원자를 포함하는 C4-C50알킬; C4-C12 시클로알킬; 중간에 산소 원자를 포함하는 C4-C12 시클로알킬; C2-C20 알케닐; 중간에 산소 원자를 포함하는 C2-C20 알케닐; 또는 C6-C12 아릴이거나; 또는 히드록시, -NH2, -NH-C1-C8 알킬, -NH-시클로헥실, -N(C1-C8알킬)2, 디시클로헥실아미노, 할로겐, C1-C20 알킬, C1-C20 알콕시, C4-C12시클로알킬, C4-C12 시클로알콕시, C2-C20알케닐, C4-C12시클로알킬, C3-C20 알키닐, C6-C12 시클로알키닐, C6-C12 아릴, 아실아미노, 아실옥시, 술포닐, 카르복시, (메트)아크릴옥시, (메트)아크릴아미노, 에 의해 치환된 C1-C20 알킬 또는 C4-C12 시클로알킬임.
- 제 1항에 있어서, 화학식(1)의 화합물 중량부당 0.2 내지 5 중량부의 화학식(2)의 화합물을 포함하는 혼합물.
- 제 1항에 있어서, 화학식(1)의 화합물에서,k가 1이고,G는 수소, C1-C18알킬, OH, C1-C18알콕시, C5-C12시클로알콕시, -COOG8, -CON(G9)(G10), 페녹시 및/또는 -OCOG11에 의해 치환된 C1-C12알킬; 글리시딜 또는 벤질이거나; 또는 G는 -(CH2CHG15-O)i-G18 또는 -CH2-CH(OH)-CH2-O-(CH2CHG15-O)i-G18 이며, 이때 i는 2 내지 12의 수이고;G8은 C1-C12알킬; C3-C12알케닐; 중간에 O를 포함하고 및/또는 OH에 의해 치환된 C6-C20알킬; C5-C12시클로알킬; C1-C4알킬시클로헥실이거나; 또는 -P(0)(OG14)2에 의해 치환된 C1-C4 알킬이고;G9 및 G10은 C4-C8알킬이고;G11은 C1-C8알킬, 시클로헥실 또는 C2-C3알케닐이거나; 또는 중간에 -O-를 포함하는 C3-C20알킬이거나; 또는 중간에 -0-를 포함하고 OH에 의해 치환된 C3-C20알킬이고,G14는 C1-C4알킬이며;G15는 H이고; 그리고G16은 수소, C1-C18알킬, 페닐 또는 C7-C10 알킬페닐이고;또 화학식(2)의 화합물에서,R6 내지 R15는 서로 독립해서 H, C1-C12알킬 또는 Cl이며;R11, R12 및 R13은, q가 0인 경우, OH 및 OY를 나타내고;p는 1이고;X 및 Y는 서로 독립해서 Ry; Rx에 의해 치환된 C2-C12알킬; 중간에 산소 원자를 포함하고 Rx에 의해 치환된 C3-C30알킬이고;Rx는 히드록시; C1-C12알킬; C6-C12시클로알킬; C1-C20알콕시; C6-C12시클로알콕시; 페닐; -ORz; Rz; 알릴; 또는 히드록시, C1-C12알킬, C1-C12알콕시, 카르복시에 의해 치환된 C1-C20알킬, C2-C20알콕시 또는 시클로헥실이고;Ry는 수소; C1-C12알킬; C6-C12시클로알킬; 페닐; -Rz; 알릴; 또는 히드록시, C1-C12알킬, C1-C12알콕시 또는 카르복시에 의해 치환된 C1-C20알킬 또는 시클로헥실이며;RZ는 -COR'; -COOR'; -CONR'R"; -CO-CH=CH2; -CO-C(CH3)=CH2 이고;R' 및 R"는 서로 독립해서 수소; C1-C20알킬; 중간에 산소 원자를 포함하는 C4-C20알킬; C4-C12 시클로알킬; 또는 히드록시, C1-C12알킬, C1-C12알콕시 또는 카르복시에 의해 치환된 C2-C20 알킬 또는 시클로헥실인 혼합물.
- A) 광, 산소 및/또는 열에 의한 손상에 민감한 유기 물질 및B) 안정화제로서 화학식(1)의 화합물 및 화학식(2)의 화합물을 포함하는 혼합물을 포함하는 조성물.
- 제 4항에 있어서, 성분 A 100 중량부당 0.01 내지 15 중량부의 성분 B를 포함하는 조성물.
- 제 4항에 있어서, 성분 A로서 열가소성 중합체, 도료용 결합제 또는 사진 물질을 포함하는 조성물.
- 제 6항에 있어서, 성분 A로서 도료용 결합제 또는 열가소성 중합체 및 추가의 성분으로서 입체 장애 아민 및/또는 2-히드록시페닐-2H-벤조트리아졸 유형의 광 안정화제로 구성된 군으로 부터 선택된 안정화제를 포함하는 조성물.
- 화학식(1)의 화합물 및 화학식(2)의 화합물을 포함하는 제 1항에 따른 혼합물을 안정화제로서 유기 물질에 부가하는 것을 포함하는 광, 산소 및/또는 열에 의한 손상으로 부터 유기 물질을 안정화시키는 방법.
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-
1997
- 1997-09-04 BE BE9700719A patent/BE1012529A3/fr not_active IP Right Cessation
- 1997-09-05 AU AU36843/97A patent/AU727251B2/en not_active Ceased
- 1997-09-08 US US08/925,014 patent/US6060543A/en not_active Expired - Lifetime
- 1997-09-09 KR KR1019970046267A patent/KR100457006B1/ko not_active Expired - Lifetime
- 1997-09-10 IT IT97MI002058A patent/IT1295008B1/it active IP Right Grant
- 1997-09-10 GB GB9719141A patent/GB2317893B/en not_active Expired - Lifetime
- 1997-09-10 DE DE19739797A patent/DE19739797B4/de not_active Expired - Lifetime
- 1997-09-10 ES ES009701910A patent/ES2142242B1/es not_active Expired - Fee Related
- 1997-09-11 TW TW086113165A patent/TW376409B/zh not_active IP Right Cessation
- 1997-09-11 CA CA002215134A patent/CA2215134C/en not_active Expired - Lifetime
- 1997-09-11 FR FR9711289A patent/FR2753448B1/fr not_active Expired - Lifetime
- 1997-09-11 SE SE9703289A patent/SE510502C2/sv not_active IP Right Cessation
- 1997-09-12 NL NL1007028A patent/NL1007028C2/nl not_active IP Right Cessation
- 1997-09-13 MY MYPI97004258A patent/MY116146A/en unknown
- 1997-09-15 CN CNB971184534A patent/CN1185294C/zh not_active Expired - Lifetime
- 1997-09-15 BR BR9704713A patent/BR9704713A/pt not_active IP Right Cessation
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Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR101541431B1 (ko) * | 2007-01-15 | 2015-08-03 | 시바 홀딩 인크 | 2-하이드록시 페닐 트리아진에 의해 uv 안정화된 착색된 투명 피복물 |
Also Published As
| Publication number | Publication date |
|---|---|
| SE510502C2 (sv) | 1999-05-31 |
| CA2215134A1 (en) | 1998-03-13 |
| SE9703289L (sv) | 1998-03-14 |
| NL1007028A1 (nl) | 1998-03-16 |
| ES2142242B1 (es) | 2000-11-16 |
| US6060543A (en) | 2000-05-09 |
| NL1007028C2 (nl) | 2000-08-08 |
| SE9703289D0 (sv) | 1997-09-11 |
| KR19980024436A (ko) | 1998-07-06 |
| MX9706950A (es) | 1998-08-30 |
| GB2317893A (en) | 1998-04-08 |
| ES2142242A1 (es) | 2000-04-01 |
| JP4379640B2 (ja) | 2009-12-09 |
| BR9704713A (pt) | 1998-12-15 |
| CA2215134C (en) | 2007-08-21 |
| ITMI972058A1 (it) | 1999-03-10 |
| AU3684397A (en) | 1998-03-19 |
| DE19739797A1 (de) | 1998-03-19 |
| FR2753448A1 (fr) | 1998-03-20 |
| BE1012529A3 (fr) | 2000-12-05 |
| GB9719141D0 (en) | 1997-11-12 |
| CN1177608A (zh) | 1998-04-01 |
| FR2753448B1 (fr) | 2002-02-01 |
| MY116146A (en) | 2003-11-28 |
| CN1185294C (zh) | 2005-01-19 |
| GB2317893B (en) | 2000-11-08 |
| DE19739797B4 (de) | 2008-06-05 |
| AU727251B2 (en) | 2000-12-07 |
| JPH1095974A (ja) | 1998-04-14 |
| TW376409B (en) | 1999-12-11 |
| IT1295008B1 (it) | 1999-04-27 |
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