BE1009749A3 - Composes de piperidine et de triazine contenant des groupes silicies, composition les contenant et procede les utilisant pour stabiliser des matieres organiques. - Google Patents
Composes de piperidine et de triazine contenant des groupes silicies, composition les contenant et procede les utilisant pour stabiliser des matieres organiques. Download PDFInfo
- Publication number
 - BE1009749A3 BE1009749A3 BE9500983A BE9500983A BE1009749A3 BE 1009749 A3 BE1009749 A3 BE 1009749A3 BE 9500983 A BE9500983 A BE 9500983A BE 9500983 A BE9500983 A BE 9500983A BE 1009749 A3 BE1009749 A3 BE 1009749A3
 - Authority
 - BE
 - Belgium
 - Prior art keywords
 - group
 - formula
 - tert
 - butyl
 - bis
 - Prior art date
 
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- 239000000203 mixture Substances 0.000 title claims description 40
 - 239000011368 organic material Substances 0.000 title claims description 13
 - 238000000034 method Methods 0.000 title claims description 11
 - NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical class C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 title description 5
 - 230000006641 stabilisation Effects 0.000 title description 2
 - 238000011105 stabilization Methods 0.000 title description 2
 - KWAYGHBLGWNQBS-UHFFFAOYSA-N silicon;triazine Chemical group [Si].C1=CN=NN=C1 KWAYGHBLGWNQBS-UHFFFAOYSA-N 0.000 title 1
 - -1 2,2,6,6-tetramethyl-4-piperidyl group Chemical group 0.000 claims abstract description 98
 - 150000001875 compounds Chemical class 0.000 claims abstract description 44
 - 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims abstract description 16
 - 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 15
 - 239000001257 hydrogen Substances 0.000 claims abstract description 15
 - 125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract description 14
 - 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims abstract description 6
 - 125000000217 alkyl group Chemical group 0.000 claims description 18
 - 239000004743 Polypropylene Substances 0.000 claims description 14
 - 125000003545 alkoxy group Chemical group 0.000 claims description 10
 - 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 10
 - 229920001155 polypropylene Polymers 0.000 claims description 10
 - 125000003884 phenylalkyl group Chemical group 0.000 claims description 7
 - 239000004698 Polyethylene Substances 0.000 claims description 6
 - 239000000654 additive Substances 0.000 claims description 6
 - 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 6
 - 229920000573 polyethylene Polymers 0.000 claims description 6
 - 229920001059 synthetic polymer Polymers 0.000 claims description 6
 - 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 claims description 5
 - 230000003647 oxidation Effects 0.000 claims description 5
 - 238000007254 oxidation reaction Methods 0.000 claims description 5
 - 125000004209 (C1-C8) alkyl group Chemical group 0.000 claims description 4
 - 125000000753 cycloalkyl group Chemical group 0.000 claims description 4
 - 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 4
 - 125000002252 acyl group Chemical group 0.000 claims description 3
 - 125000003277 amino group Chemical group 0.000 claims description 3
 - 125000000000 cycloalkoxy group Chemical group 0.000 claims description 3
 - 230000000087 stabilizing effect Effects 0.000 claims description 2
 - 230000015556 catabolic process Effects 0.000 claims 2
 - 238000006731 degradation reaction Methods 0.000 claims 2
 - 125000004400 (C1-C12) alkyl group Chemical group 0.000 claims 1
 - PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 54
 - 229920001577 copolymer Polymers 0.000 description 36
 - 229920000642 polymer Polymers 0.000 description 19
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 - 229910052757 nitrogen Inorganic materials 0.000 description 15
 - NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 13
 - 239000004952 Polyamide Substances 0.000 description 13
 - 229920002647 polyamide Polymers 0.000 description 13
 - LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 12
 - OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 12
 - MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 12
 - 229920001684 low density polyethylene Polymers 0.000 description 12
 - 239000004702 low-density polyethylene Substances 0.000 description 12
 - VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 10
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 - 150000002148 esters Chemical class 0.000 description 9
 - 239000000463 material Substances 0.000 description 9
 - 229920002857 polybutadiene Polymers 0.000 description 9
 - 239000003381 stabilizer Substances 0.000 description 9
 - 239000005062 Polybutadiene Substances 0.000 description 8
 - 150000001412 amines Chemical class 0.000 description 8
 - KBPLFHHGFOOTCA-UHFFFAOYSA-N caprylic alcohol Natural products CCCCCCCCO KBPLFHHGFOOTCA-UHFFFAOYSA-N 0.000 description 8
 - GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 description 8
 - 239000004417 polycarbonate Substances 0.000 description 8
 - 229920000122 acrylonitrile butadiene styrene Polymers 0.000 description 7
 - 150000001993 dienes Chemical class 0.000 description 7
 - 239000000835 fiber Substances 0.000 description 7
 - WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 7
 - 229920006324 polyoxymethylene Polymers 0.000 description 7
 - KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 6
 - WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 6
 - PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 6
 - 239000007983 Tris buffer Substances 0.000 description 6
 - 239000007859 condensation product Substances 0.000 description 6
 - DMBHHRLKUKUOEG-UHFFFAOYSA-N diphenylamine Chemical compound C=1C=CC=CC=1NC1=CC=CC=C1 DMBHHRLKUKUOEG-UHFFFAOYSA-N 0.000 description 6
 - NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 description 6
 - TVMXDCGIABBOFY-UHFFFAOYSA-N n-Octanol Natural products CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 6
 - 229920000915 polyvinyl chloride Polymers 0.000 description 6
 - 239000004800 polyvinyl chloride Substances 0.000 description 6
 - CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 5
 - ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 5
 - WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 5
 - 239000003054 catalyst Substances 0.000 description 5
 - 229920001903 high density polyethylene Polymers 0.000 description 5
 - 239000004700 high-density polyethylene Substances 0.000 description 5
 - 238000002360 preparation method Methods 0.000 description 5
 - 150000005846 sugar alcohols Polymers 0.000 description 5
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 - DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 description 4
 - ALVZNPYWJMLXKV-UHFFFAOYSA-N 1,9-Nonanediol Chemical compound OCCCCCCCCCO ALVZNPYWJMLXKV-UHFFFAOYSA-N 0.000 description 4
 - GXURZKWLMYOCDX-UHFFFAOYSA-N 2,2-bis(hydroxymethyl)propane-1,3-diol;dihydroxyphosphanyl dihydrogen phosphite Chemical compound OP(O)OP(O)O.OCC(CO)(CO)CO GXURZKWLMYOCDX-UHFFFAOYSA-N 0.000 description 4
 - KXPXKNBDCUOENF-UHFFFAOYSA-N 2-(Octylthio)ethanol Chemical compound CCCCCCCCSCCO KXPXKNBDCUOENF-UHFFFAOYSA-N 0.000 description 4
 - ZPIRWAHWDCHWLM-UHFFFAOYSA-N 2-dodecylsulfanylethanol Chemical compound CCCCCCCCCCCCSCCO ZPIRWAHWDCHWLM-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
 - 229920000877 Melamine resin Polymers 0.000 description 4
 - 229910019032 PtCl2 Inorganic materials 0.000 description 4
 - GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 4
 - ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 4
 - 239000002253 acid Substances 0.000 description 4
 - 150000001252 acrylic acid derivatives Chemical class 0.000 description 4
 - 150000001336 alkenes Chemical class 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
 - 125000006309 butyl amino group Chemical group 0.000 description 4
 - DIOQZVSQGTUSAI-UHFFFAOYSA-N decane Chemical compound CCCCCCCCCC DIOQZVSQGTUSAI-UHFFFAOYSA-N 0.000 description 4
 - 229920001971 elastomer Polymers 0.000 description 4
 - 229940093476 ethylene glycol Drugs 0.000 description 4
 - XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 description 4
 - 229910052751 metal Inorganic materials 0.000 description 4
 - 239000002184 metal Substances 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
 - SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 4
 - 229940117969 neopentyl glycol Drugs 0.000 description 4
 - 239000003921 oil Substances 0.000 description 4
 - 229920001707 polybutylene terephthalate Polymers 0.000 description 4
 - 238000006116 polymerization reaction Methods 0.000 description 4
 - 239000004814 polyurethane Substances 0.000 description 4
 - 239000000047 product Substances 0.000 description 4
 - QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 4
 - 229960004063 propylene glycol Drugs 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
 - 239000007787 solid Substances 0.000 description 4
 - 239000000243 solution Substances 0.000 description 4
 - 239000002904 solvent Substances 0.000 description 4
 - 229920001897 terpolymer Polymers 0.000 description 4
 - 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 4
 - YODZTKMDCQEPHD-UHFFFAOYSA-N thiodiglycol Chemical compound OCCSCCO YODZTKMDCQEPHD-UHFFFAOYSA-N 0.000 description 4
 - 239000011732 tocopherol Substances 0.000 description 4
 - ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 4
 - 125000000026 trimethylsilyl group Chemical group [H]C([H])([H])[Si]([*])(C([H])([H])[H])C([H])([H])[H] 0.000 description 4
 - 239000008096 xylene Substances 0.000 description 4
 - ZEBMSMUPGIOANU-UHFFFAOYSA-N (3,5-ditert-butyl-4-hydroxyphenyl)methylphosphonic acid Chemical compound CC(C)(C)C1=CC(CP(O)(O)=O)=CC(C(C)(C)C)=C1O ZEBMSMUPGIOANU-UHFFFAOYSA-N 0.000 description 3
 - 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 3
 - VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 3
 - RXFCIXRFAJRBSG-UHFFFAOYSA-N 3,2,3-tetramine Chemical compound NCCCNCCNCCCN RXFCIXRFAJRBSG-UHFFFAOYSA-N 0.000 description 3
 - YEXOWHQZWLCHHD-UHFFFAOYSA-N 3,5-ditert-butyl-4-hydroxybenzoic acid Chemical compound CC(C)(C)C1=CC(C(O)=O)=CC(C(C)(C)C)=C1O YEXOWHQZWLCHHD-UHFFFAOYSA-N 0.000 description 3
 - CKPKHTKLLYPGFM-UHFFFAOYSA-N 6,6-dimethylheptane-1,1-diol Chemical compound CC(CCCCC(O)O)(C)C CKPKHTKLLYPGFM-UHFFFAOYSA-N 0.000 description 3
 - 229920002943 EPDM rubber Polymers 0.000 description 3
 - 229920002396 Polyurea Polymers 0.000 description 3
 - XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical group [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 3
 - 150000007513 acids Chemical class 0.000 description 3
 - 125000001931 aliphatic group Chemical group 0.000 description 3
 - XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 description 3
 - 239000003963 antioxidant agent Substances 0.000 description 3
 - 235000006708 antioxidants Nutrition 0.000 description 3
 - 125000003118 aryl group Chemical group 0.000 description 3
 - QRUDEWIWKLJBPS-UHFFFAOYSA-N benzotriazole Chemical compound C1=CC=C2N[N][N]C2=C1 QRUDEWIWKLJBPS-UHFFFAOYSA-N 0.000 description 3
 - 239000012964 benzotriazole Substances 0.000 description 3
 - 230000003197 catalytic effect Effects 0.000 description 3
 - 150000001991 dicarboxylic acids Chemical class 0.000 description 3
 - HQQADJVZYDDRJT-UHFFFAOYSA-N ethene;prop-1-ene Chemical group C=C.CC=C HQQADJVZYDDRJT-UHFFFAOYSA-N 0.000 description 3
 - 229920006242 ethylene acrylic acid copolymer Polymers 0.000 description 3
 - 239000005038 ethylene vinyl acetate Substances 0.000 description 3
 - 229920000554 ionomer Polymers 0.000 description 3
 - ZFSLODLOARCGLH-UHFFFAOYSA-N isocyanuric acid Chemical compound OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 0.000 description 3
 - 239000003446 ligand Substances 0.000 description 3
 - 150000002739 metals Chemical class 0.000 description 3
 - 150000005673 monoalkenes Chemical class 0.000 description 3
 - 239000000178 monomer Substances 0.000 description 3
 - 150000002815 nickel Chemical class 0.000 description 3
 - 229910052759 nickel Inorganic materials 0.000 description 3
 - 235000019198 oils Nutrition 0.000 description 3
 - 229920000058 polyacrylate Polymers 0.000 description 3
 - 229920000728 polyester Polymers 0.000 description 3
 - 229920000570 polyether Polymers 0.000 description 3
 - 229920001843 polymethylhydrosiloxane Polymers 0.000 description 3
 - 229920000098 polyolefin Polymers 0.000 description 3
 - 239000000843 powder Substances 0.000 description 3
 - 229920005989 resin Polymers 0.000 description 3
 - 239000011347 resin Substances 0.000 description 3
 - 125000004079 stearyl 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])([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])C([H])([H])[H] 0.000 description 3
 - 229960001295 tocopherol Drugs 0.000 description 3
 - 150000003918 triazines Chemical class 0.000 description 3
 - 238000005292 vacuum distillation Methods 0.000 description 3
 - 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 3
 - 239000001993 wax Substances 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
 - ZQMPWXFHAUDENN-UHFFFAOYSA-N 1,2-bis[(2-methylphenyl)amino]ethane Natural products CC1=CC=CC=C1NCCNC1=CC=CC=C1C ZQMPWXFHAUDENN-UHFFFAOYSA-N 0.000 description 2
 - YHMYGUUIMTVXNW-UHFFFAOYSA-N 1,3-dihydrobenzimidazole-2-thione Chemical compound C1=CC=C2NC(S)=NC2=C1 YHMYGUUIMTVXNW-UHFFFAOYSA-N 0.000 description 2
 - 150000005208 1,4-dihydroxybenzenes Chemical class 0.000 description 2
 - BUGAMLAPDQMYNZ-UHFFFAOYSA-N 1-(2,4,4-trimethylpentan-2-yl)-10h-phenothiazine Chemical class S1C2=CC=CC=C2NC2=C1C=CC=C2C(C)(C)CC(C)(C)C BUGAMLAPDQMYNZ-UHFFFAOYSA-N 0.000 description 2
 - HECLRDQVFMWTQS-RGOKHQFPSA-N 1755-01-7 Chemical compound C1[C@H]2[C@@H]3CC=C[C@@H]3[C@@H]1C=C2 HECLRDQVFMWTQS-RGOKHQFPSA-N 0.000 description 2
 - KGRVJHAUYBGFFP-UHFFFAOYSA-N 2,2'-Methylenebis(4-methyl-6-tert-butylphenol) Chemical compound CC(C)(C)C1=CC(C)=CC(CC=2C(=C(C=C(C)C=2)C(C)(C)C)O)=C1O KGRVJHAUYBGFFP-UHFFFAOYSA-N 0.000 description 2
 - BWJKLDGAAPQXGO-UHFFFAOYSA-N 2,2,6,6-tetramethyl-4-octadecoxypiperidine Chemical compound CCCCCCCCCCCCCCCCCCOC1CC(C)(C)NC(C)(C)C1 BWJKLDGAAPQXGO-UHFFFAOYSA-N 0.000 description 2
 - SLUKQUGVTITNSY-UHFFFAOYSA-N 2,6-di-tert-butyl-4-methoxyphenol Chemical compound COC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 SLUKQUGVTITNSY-UHFFFAOYSA-N 0.000 description 2
 - 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 2
 - SAEZGDDJKSBNPT-UHFFFAOYSA-N 3-dodecyl-1-(1,2,2,6,6-pentamethylpiperidin-4-yl)pyrrolidine-2,5-dione Chemical compound O=C1C(CCCCCCCCCCCC)CC(=O)N1C1CC(C)(C)N(C)C(C)(C)C1 SAEZGDDJKSBNPT-UHFFFAOYSA-N 0.000 description 2
 - BWDBEAQIHAEVLV-UHFFFAOYSA-N 6-methylheptan-1-ol Chemical compound CC(C)CCCCCO BWDBEAQIHAEVLV-UHFFFAOYSA-N 0.000 description 2
 - NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 2
 - 229920000178 Acrylic resin Polymers 0.000 description 2
 - 239000004925 Acrylic resin Substances 0.000 description 2
 - VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
 - UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 2
 - RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
 - OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 2
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 - TWRXJAOTZQYOKJ-UHFFFAOYSA-L Magnesium chloride Chemical compound [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 description 2
 - PEEHTFAAVSWFBL-UHFFFAOYSA-N Maleimide Chemical compound O=C1NC(=O)C=C1 PEEHTFAAVSWFBL-UHFFFAOYSA-N 0.000 description 2
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 - XQVWYOYUZDUNRW-UHFFFAOYSA-N N-Phenyl-1-naphthylamine Chemical compound C=1C=CC2=CC=CC=C2C=1NC1=CC=CC=C1 XQVWYOYUZDUNRW-UHFFFAOYSA-N 0.000 description 2
 - KEQFTVQCIQJIQW-UHFFFAOYSA-N N-Phenyl-2-naphthylamine Chemical compound C=1C=C2C=CC=CC2=CC=1NC1=CC=CC=C1 KEQFTVQCIQJIQW-UHFFFAOYSA-N 0.000 description 2
 - REYJJPSVUYRZGE-UHFFFAOYSA-N Octadecylamine Chemical compound CCCCCCCCCCCCCCCCCCN REYJJPSVUYRZGE-UHFFFAOYSA-N 0.000 description 2
 - 229910019142 PO4 Inorganic materials 0.000 description 2
 - 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 2
 - 229920002367 Polyisobutene Polymers 0.000 description 2
 - KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 2
 - XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 2
 - 239000002250 absorbent Substances 0.000 description 2
 - 230000002745 absorbent Effects 0.000 description 2
 - 229920000800 acrylic rubber Polymers 0.000 description 2
 - 239000012190 activator Substances 0.000 description 2
 - 239000001361 adipic acid Substances 0.000 description 2
 - 235000011037 adipic acid Nutrition 0.000 description 2
 - 229910052784 alkaline earth metal Inorganic materials 0.000 description 2
 - 229920000180 alkyd Polymers 0.000 description 2
 - 125000005250 alkyl acrylate group Chemical group 0.000 description 2
 - TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 2
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 - IVIIAEVMQHEPAY-UHFFFAOYSA-N tridodecyl phosphite Chemical compound CCCCCCCCCCCCOP(OCCCCCCCCCCCC)OCCCCCCCCCCCC IVIIAEVMQHEPAY-UHFFFAOYSA-N 0.000 description 1
 - CYTQBVOFDCPGCX-UHFFFAOYSA-N trimethyl phosphite Chemical compound COP(OC)OC CYTQBVOFDCPGCX-UHFFFAOYSA-N 0.000 description 1
 - CNUJLMSKURPSHE-UHFFFAOYSA-N trioctadecyl phosphite Chemical compound CCCCCCCCCCCCCCCCCCOP(OCCCCCCCCCCCCCCCCCC)OCCCCCCCCCCCCCCCCCC CNUJLMSKURPSHE-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
 - 125000002948 undecyl 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])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
 - 229920006337 unsaturated polyester resin Polymers 0.000 description 1
 - 125000003774 valeryl group Chemical group O=C([*])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
 - 235000015112 vegetable and seed oil Nutrition 0.000 description 1
 - 235000019871 vegetable fat Nutrition 0.000 description 1
 - 235000019154 vitamin C Nutrition 0.000 description 1
 - 239000011718 vitamin C Substances 0.000 description 1
 - 235000019165 vitamin E Nutrition 0.000 description 1
 - 239000011709 vitamin E Substances 0.000 description 1
 - 229940046009 vitamin E Drugs 0.000 description 1
 - 239000002023 wood Substances 0.000 description 1
 - 150000003751 zinc Chemical class 0.000 description 1
 - 239000011701 zinc Substances 0.000 description 1
 - 229910052725 zinc Inorganic materials 0.000 description 1
 - BOXSVZNGTQTENJ-UHFFFAOYSA-L zinc dibutyldithiocarbamate Chemical compound [Zn+2].CCCCN(C([S-])=S)CCCC.CCCCN(C([S-])=S)CCCC BOXSVZNGTQTENJ-UHFFFAOYSA-L 0.000 description 1
 - XOOUIPVCVHRTMJ-UHFFFAOYSA-L zinc stearate Chemical compound [Zn+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O XOOUIPVCVHRTMJ-UHFFFAOYSA-L 0.000 description 1
 - GVJHHUAWPYXKBD-IEOSBIPESA-N α-tocopherol Chemical compound OC1=C(C)C(C)=C2O[C@@](CCC[C@H](C)CCC[C@H](C)CCCC(C)C)(C)CCC2=C1C GVJHHUAWPYXKBD-IEOSBIPESA-N 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
 
Classifications
- 
        
- C—CHEMISTRY; METALLURGY
 - C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
 - C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
 - C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
 - C08G77/04—Polysiloxanes
 - C08G77/38—Polysiloxanes modified by chemical after-treatment
 - C08G77/382—Polysiloxanes modified by chemical after-treatment containing atoms other than carbon, hydrogen, oxygen or silicon
 - C08G77/388—Polysiloxanes modified by chemical after-treatment containing atoms other than carbon, hydrogen, oxygen or silicon containing nitrogen
 
 - 
        
- C—CHEMISTRY; METALLURGY
 - C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
 - C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
 - C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
 - C08G77/04—Polysiloxanes
 - C08G77/22—Polysiloxanes containing silicon bound to organic groups containing atoms other than carbon, hydrogen and oxygen
 - C08G77/26—Polysiloxanes containing silicon bound to organic groups containing atoms other than carbon, hydrogen and oxygen nitrogen-containing groups
 
 - 
        
- 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
 - C08K3/00—Use of inorganic substances as compounding ingredients
 - C08K3/18—Oxygen-containing compounds, e.g. metal carbonyls
 - C08K3/20—Oxides; Hydroxides
 - C08K3/22—Oxides; Hydroxides of metals
 
 - 
        
- 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
 - C08K5/09—Carboxylic acids; Metal salts thereof; Anhydrides thereof
 - C08K5/098—Metal salts of carboxylic acids
 
 - 
        
- 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
 - C08K5/49—Phosphorus-containing compounds
 
 - 
        
- 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
 - C08K5/49—Phosphorus-containing compounds
 - C08K5/51—Phosphorus bound to oxygen
 
 - 
        
- C—CHEMISTRY; METALLURGY
 - C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
 - C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
 - C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
 - C08L23/02—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
 
 - 
        
- C—CHEMISTRY; METALLURGY
 - C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
 - C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
 - C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
 - C08L23/02—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
 - C08L23/04—Homopolymers or copolymers of ethene
 - C08L23/06—Polyethene
 
 - 
        
- C—CHEMISTRY; METALLURGY
 - C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
 - C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
 - C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
 - C08L23/02—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
 - C08L23/10—Homopolymers or copolymers of propene
 
 - 
        
- C—CHEMISTRY; METALLURGY
 - C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
 - C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
 - C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
 - C08L23/02—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
 - C08L23/10—Homopolymers or copolymers of propene
 - C08L23/12—Polypropene
 
 - 
        
- C—CHEMISTRY; METALLURGY
 - C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
 - C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
 - C08L83/00—Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon only; Compositions of derivatives of such polymers
 
 - 
        
- C—CHEMISTRY; METALLURGY
 - C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
 - C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
 - C08L2203/00—Applications
 - C08L2203/12—Applications used for fibers
 
 
Landscapes
- Chemical & Material Sciences (AREA)
 - Health & Medical Sciences (AREA)
 - Chemical Kinetics & Catalysis (AREA)
 - Medicinal Chemistry (AREA)
 - Polymers & Plastics (AREA)
 - Organic Chemistry (AREA)
 - General Chemical & Material Sciences (AREA)
 - Compositions Of Macromolecular Compounds (AREA)
 - Laminated Bodies (AREA)
 - Silicon Polymers (AREA)
 
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title | 
|---|---|---|---|
| ITMI942429A IT1271133B (it) | 1994-11-30 | 1994-11-30 | Composti piperidino triazinici contenenti gruppi silanici come stabilizzanti per materiali organici | 
Publications (1)
| Publication Number | Publication Date | 
|---|---|
| BE1009749A3 true BE1009749A3 (fr) | 1997-07-01 | 
Family
ID=11369940
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date | 
|---|---|---|---|
| BE9500983A BE1009749A3 (fr) | 1994-11-30 | 1995-11-30 | Composes de piperidine et de triazine contenant des groupes silicies, composition les contenant et procede les utilisant pour stabiliser des matieres organiques. | 
Country Status (11)
| Country | Link | 
|---|---|
| JP (1) | JPH08225650A (forum.php) | 
| KR (1) | KR960017676A (forum.php) | 
| BE (1) | BE1009749A3 (forum.php) | 
| CA (1) | CA2163956A1 (forum.php) | 
| DE (1) | DE19544114A1 (forum.php) | 
| ES (1) | ES2102329B1 (forum.php) | 
| FR (1) | FR2727419B1 (forum.php) | 
| GB (1) | GB2295619B (forum.php) | 
| IT (1) | IT1271133B (forum.php) | 
| NL (1) | NL1001781C2 (forum.php) | 
| TW (1) | TW303380B (forum.php) | 
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title | 
|---|---|---|---|---|
| DE60002859T2 (de) | 1999-04-27 | 2003-12-04 | Ciba Speciality Chemicals Holding Inc., Basel | Polysilanstabilisatoren mit sterisch gehinderten aminogruppen | 
| NO325797B1 (no) * | 2005-10-14 | 2008-07-21 | Nor X Ind As | Lysbeskyttelsesmiddel basert på organisk/uorganisk hybridpolymer, fremgangsmåte til fremstilling og anvendelse av samme | 
| FR2921663A1 (fr) * | 2007-10-02 | 2009-04-03 | Bluestar Silicones France Soc | Polyorganosiloxanes a fonction piperidine depourvus de toxicite par contact cutane et utilisation de ces derniers dans des compositions cosmetiques | 
| JP5640471B2 (ja) * | 2010-06-02 | 2014-12-17 | Jsr株式会社 | 液晶配向剤、液晶配向膜、液晶配向膜の形成方法及び液晶表示素子 | 
| JP5781511B2 (ja) | 2011-02-04 | 2015-09-24 | 株式会社Adeka | ヒンダードアミン骨格を有する化合物及び樹脂組成物 | 
| CN114854023A (zh) * | 2022-05-07 | 2022-08-05 | 宿迁联宏新材料有限公司 | 一种聚烯烃树脂用光稳定剂及其制备方法和应用 | 
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title | 
|---|---|---|---|---|
| EP0461071A1 (en) * | 1990-06-06 | 1991-12-11 | Ciba-Geigy Ag | Piperidine-triazine compounds containing silane groups, for use as stabilizers for organic materials | 
| EP0502821A1 (de) * | 1991-03-05 | 1992-09-09 | Ciba-Geigy Ag | Silylierte 2-(2-Hydroxyphenyl)-4,6-diaryl-1,3,5-triazine | 
| EP0659930A1 (fr) * | 1993-12-27 | 1995-06-28 | Rhone-Poulenc Chimie | Procédé d'adoucissage textile non jaunissant dans lequel, on utilise une composition comprenant un polyorganosiloxane | 
- 
        1994
        
- 1994-11-30 IT ITMI942429A patent/IT1271133B/it active IP Right Grant
 
 - 
        1995
        
- 1995-10-30 TW TW084111512A patent/TW303380B/zh active
 - 1995-11-24 GB GB9524075A patent/GB2295619B/en not_active Expired - Fee Related
 - 1995-11-27 DE DE19544114A patent/DE19544114A1/de not_active Withdrawn
 - 1995-11-28 CA CA002163956A patent/CA2163956A1/en not_active Abandoned
 - 1995-11-28 FR FR9514088A patent/FR2727419B1/fr not_active Expired - Fee Related
 - 1995-11-28 KR KR1019950046060A patent/KR960017676A/ko not_active Withdrawn
 - 1995-11-29 JP JP7334055A patent/JPH08225650A/ja active Pending
 - 1995-11-29 ES ES09502353A patent/ES2102329B1/es not_active Expired - Lifetime
 - 1995-11-29 NL NL1001781A patent/NL1001781C2/nl not_active IP Right Cessation
 - 1995-11-30 BE BE9500983A patent/BE1009749A3/fr not_active IP Right Cessation
 
 
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title | 
|---|---|---|---|---|
| EP0461071A1 (en) * | 1990-06-06 | 1991-12-11 | Ciba-Geigy Ag | Piperidine-triazine compounds containing silane groups, for use as stabilizers for organic materials | 
| EP0502821A1 (de) * | 1991-03-05 | 1992-09-09 | Ciba-Geigy Ag | Silylierte 2-(2-Hydroxyphenyl)-4,6-diaryl-1,3,5-triazine | 
| EP0659930A1 (fr) * | 1993-12-27 | 1995-06-28 | Rhone-Poulenc Chimie | Procédé d'adoucissage textile non jaunissant dans lequel, on utilise une composition comprenant un polyorganosiloxane | 
Also Published As
| Publication number | Publication date | 
|---|---|
| JPH08225650A (ja) | 1996-09-03 | 
| FR2727419B1 (fr) | 1997-12-12 | 
| NL1001781C2 (nl) | 1997-03-25 | 
| ITMI942429A1 (it) | 1996-05-30 | 
| NL1001781A1 (nl) | 1996-05-30 | 
| IT1271133B (it) | 1997-05-26 | 
| ES2102329A1 (es) | 1997-07-16 | 
| ITMI942429A0 (it) | 1994-11-30 | 
| KR960017676A (ko) | 1996-06-17 | 
| CA2163956A1 (en) | 1996-05-31 | 
| ES2102329B1 (es) | 1998-04-01 | 
| FR2727419A1 (fr) | 1996-05-31 | 
| DE19544114A1 (de) | 1996-06-05 | 
| TW303380B (forum.php) | 1997-04-21 | 
| GB9524075D0 (en) | 1996-01-24 | 
| GB2295619A (en) | 1996-06-05 | 
| GB2295619B (en) | 1997-02-19 | 
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Legal Events
| Date | Code | Title | Description | 
|---|---|---|---|
| RE | Patent lapsed | 
             Owner name: CIBA SPECIALTY CHEMICALS HOLDING INC. Effective date: 19981130  |