NL1009260C2 - Triazine-derivaten die 2,2,6,6-tetramethyl-4-piperidylgroepen bevatten. - Google Patents

Triazine-derivaten die 2,2,6,6-tetramethyl-4-piperidylgroepen bevatten. Download PDF

Info

Publication number: NL1009260C2
Authority: NL; Netherlands
Prior art keywords: formula; alkyl; group; groups; hydrogen
Prior art date: 1997-05-27

Application number

NL1009260A

Other languages

English (en)

Dutch (nl)

Other versions

NL1009260A1 (nl

Inventor

Gianluca Ferri

Alessandro Zeddo

Original Assignee

Ciba Sc Holding 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.)

1997-05-27

Filing date

1998-05-26

Publication date

1999-09-24

1998-05-26 Application filed by Ciba Sc Holding Ag filed Critical Ciba Sc Holding Ag

1998-12-01 Publication of NL1009260A1 publication Critical patent/NL1009260A1/xx

1999-09-24 Application granted granted Critical

1999-09-24 Publication of NL1009260C2 publication Critical patent/NL1009260C2/nl

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-1 2,2,6,6-tetramethyl-4-piperidyl groups Chemical group 0.000 title claims description 184
150000003918 triazines Chemical class 0.000 title description 4
150000001875 compounds Chemical class 0.000 claims description 134
239000000203 mixture Substances 0.000 claims description 90
125000000217 alkyl group Chemical group 0.000 claims description 60
229910052739 hydrogen Inorganic materials 0.000 claims description 58
239000001257 hydrogen Substances 0.000 claims description 38
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 28
150000002431 hydrogen Chemical class 0.000 claims description 27
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 24
239000004743 Polypropylene Substances 0.000 claims description 21
125000003545 alkoxy group Chemical group 0.000 claims description 19
125000002947 alkylene group Chemical group 0.000 claims description 17
238000000034 method Methods 0.000 claims description 17
229920001155 polypropylene Polymers 0.000 claims description 17
239000011368 organic material Substances 0.000 claims description 15
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 12
229910052799 carbon Inorganic materials 0.000 claims description 12
125000000753 cycloalkyl group Chemical group 0.000 claims description 12
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 11
239000004698 Polyethylene Substances 0.000 claims description 10
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 10
229920000573 polyethylene Polymers 0.000 claims description 10
125000003031 C5-C7 cycloalkylene group Chemical group 0.000 claims description 8
125000000000 cycloalkoxy group Chemical group 0.000 claims description 7
125000003884 phenylalkyl group Chemical group 0.000 claims description 7
230000003647 oxidation Effects 0.000 claims description 6
238000007254 oxidation reaction Methods 0.000 claims description 6
229920001059 synthetic polymer Polymers 0.000 claims description 6
241001104043 Syringa Species 0.000 claims description 5
235000004338 Syringa vulgaris Nutrition 0.000 claims description 5
125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 claims description 5
125000002252 acyl group Chemical group 0.000 claims description 5
125000003342 alkenyl group Chemical group 0.000 claims description 5
125000004573 morpholin-4-yl group Chemical group N1(CCOCC1)* 0.000 claims description 5
125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 5
125000006702 (C1-C18) alkyl group Chemical group 0.000 claims description 4
125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 claims description 4
125000004200 2-methoxyethyl group Chemical group [H]C([H])([H])OC([H])([H])C([H])([H])* 0.000 claims description 4
125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims description 4
230000015556 catabolic process Effects 0.000 claims description 4
238000006731 degradation reaction Methods 0.000 claims description 4
230000000087 stabilizing effect Effects 0.000 claims description 4
125000004400 (C1-C12) alkyl group Chemical group 0.000 claims description 3
125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims description 3
125000004956 cyclohexylene group Chemical group 0.000 claims description 3
125000002933 cyclohexyloxy group Chemical group C1(CCCCC1)O* 0.000 claims description 3
125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 claims description 3
125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 claims description 3
125000006273 (C1-C3) alkyl group Chemical group 0.000 claims 1
125000004191 (C1-C6) alkoxy group Chemical group 0.000 claims 1
125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 claims 1
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 57
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 54
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 45
229910052757 nitrogen Inorganic materials 0.000 description 45
239000000243 solution Substances 0.000 description 44
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 37
229920001577 copolymer Polymers 0.000 description 36
229920000642 polymer Polymers 0.000 description 21
239000003381 stabilizer Substances 0.000 description 20
238000003756 stirring Methods 0.000 description 19
JYEUMXHLPRZUAT-UHFFFAOYSA-N 1,2,3-triazine Chemical compound C1=CN=NN=C1 JYEUMXHLPRZUAT-UHFFFAOYSA-N 0.000 description 17
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 15
150000002148 esters Chemical class 0.000 description 15
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 14
ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 14
NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 13
239000007983 Tris buffer Substances 0.000 description 13
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 12
239000005977 Ethylene Substances 0.000 description 12
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 12
MGNCLNQXLYJVJD-UHFFFAOYSA-N cyanuric chloride Chemical compound ClC1=NC(Cl)=NC(Cl)=N1 MGNCLNQXLYJVJD-UHFFFAOYSA-N 0.000 description 12
MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 12
238000002360 preparation method Methods 0.000 description 12
239000000047 product Substances 0.000 description 12
239000004952 Polyamide Substances 0.000 description 11
150000001412 amines Chemical class 0.000 description 11
229920002647 polyamide Polymers 0.000 description 11
238000002844 melting Methods 0.000 description 9
230000008018 melting Effects 0.000 description 9
229920002857 polybutadiene Polymers 0.000 description 9
239000005062 Polybutadiene Substances 0.000 description 8
239000008346 aqueous phase Substances 0.000 description 8
KBPLFHHGFOOTCA-UHFFFAOYSA-N caprylic alcohol Natural products CCCCCCCCO KBPLFHHGFOOTCA-UHFFFAOYSA-N 0.000 description 8
238000006243 chemical reaction Methods 0.000 description 8
239000000460 chlorine Substances 0.000 description 8
229920001684 low density polyethylene Polymers 0.000 description 8
239000004702 low-density polyethylene Substances 0.000 description 8
229910052751 metal Inorganic materials 0.000 description 8
GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 description 8
239000012074 organic phase Substances 0.000 description 8
239000004417 polycarbonate Substances 0.000 description 8
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 7
PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 7
229920000122 acrylonitrile butadiene styrene Polymers 0.000 description 7
239000007859 condensation product Substances 0.000 description 7
150000001993 dienes Chemical class 0.000 description 7
239000000835 fiber Substances 0.000 description 7
229920001903 high density polyethylene Polymers 0.000 description 7
239000004700 high-density polyethylene Substances 0.000 description 7
239000002184 metal Substances 0.000 description 7
239000000843 powder Substances 0.000 description 7
239000008096 xylene Substances 0.000 description 7
XBDQKXXYIPTUBI-UHFFFAOYSA-N Propionic acid Chemical class CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 6
GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 6
239000000654 additive Substances 0.000 description 6
239000003054 catalyst 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
229920006324 polyoxymethylene Polymers 0.000 description 6
239000004800 polyvinyl chloride Substances 0.000 description 6
229920000915 polyvinyl chloride Polymers 0.000 description 6
150000001252 acrylic acid derivatives Chemical class 0.000 description 5
WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 5
125000004432 carbon atom Chemical group C* 0.000 description 5
229920001971 elastomer Polymers 0.000 description 5
239000000463 material Substances 0.000 description 5
FDAKZQLBIFPGSV-UHFFFAOYSA-N n-butyl-2,2,6,6-tetramethylpiperidin-4-amine Chemical compound CCCCNC1CC(C)(C)NC(C)(C)C1 FDAKZQLBIFPGSV-UHFFFAOYSA-N 0.000 description 5
239000003921 oil Substances 0.000 description 5
239000000049 pigment Substances 0.000 description 5
229920000728 polyester Polymers 0.000 description 5
150000005846 sugar alcohols Polymers 0.000 description 5
229920002554 vinyl polymer Polymers 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
ACZGCWSMSTYWDQ-UHFFFAOYSA-N 3h-1-benzofuran-2-one Chemical class C1=CC=C2OC(=O)CC2=C1 ACZGCWSMSTYWDQ-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
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
OFOBLEOULBTSOW-UHFFFAOYSA-L Malonate Chemical compound [O-]C(=O)CC([O-])=O OFOBLEOULBTSOW-UHFFFAOYSA-L 0.000 description 4
229920000877 Melamine resin Polymers 0.000 description 4
239000004721 Polyphenylene oxide Substances 0.000 description 4
JWUXJYZVKZKLTJ-UHFFFAOYSA-N Triacetonamine Chemical compound CC1(C)CC(=O)CC(C)(C)N1 JWUXJYZVKZKLTJ-UHFFFAOYSA-N 0.000 description 4
XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 4
239000002253 acid Substances 0.000 description 4
125000003118 aryl group Chemical group 0.000 description 4
QRUDEWIWKLJBPS-UHFFFAOYSA-N benzotriazole Chemical compound C1=CC=C2N[N][N]C2=C1 QRUDEWIWKLJBPS-UHFFFAOYSA-N 0.000 description 4
239000012964 benzotriazole Substances 0.000 description 4
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 4
239000003795 chemical substances by application Substances 0.000 description 4
DIOQZVSQGTUSAI-UHFFFAOYSA-N decane Chemical compound CCCCCCCCCC DIOQZVSQGTUSAI-UHFFFAOYSA-N 0.000 description 4
150000004985 diamines Chemical class 0.000 description 4
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 4
239000008187 granular material Substances 0.000 description 4
NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 description 4
XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 description 4
239000000155 melt Substances 0.000 description 4
JKQOBWVOAYFWKG-UHFFFAOYSA-N molybdenum trioxide Chemical compound O=[Mo](=O)=O JKQOBWVOAYFWKG-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
SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 4
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229920001707 polybutylene terephthalate Polymers 0.000 description 4
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125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 4
150000003839 salts Chemical class 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
ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-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 3
MSXVEPNJUHWQHW-UHFFFAOYSA-N 2-methylbutan-2-ol Chemical compound CCC(C)(C)O MSXVEPNJUHWQHW-UHFFFAOYSA-N 0.000 description 3
RXFCIXRFAJRBSG-UHFFFAOYSA-N 3,2,3-tetramine Chemical compound NCCCNCCNCCCN RXFCIXRFAJRBSG-UHFFFAOYSA-N 0.000 description 3
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CKPKHTKLLYPGFM-UHFFFAOYSA-N 6,6-dimethylheptane-1,1-diol Chemical compound CC(CCCCC(O)O)(C)C CKPKHTKLLYPGFM-UHFFFAOYSA-N 0.000 description 3
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ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 3
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239000003963 antioxidant agent Substances 0.000 description 3
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238000010586 diagram Methods 0.000 description 3
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229920000554 ionomer Polymers 0.000 description 3
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GXFQBBOZTNQHMW-UHFFFAOYSA-N n'-(2,2,6,6-tetramethylpiperidin-4-yl)hexane-1,6-diamine Chemical compound CC1(C)CC(NCCCCCCN)CC(C)(C)N1 GXFQBBOZTNQHMW-UHFFFAOYSA-N 0.000 description 3
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FPEXZUSKGJEHCF-UHFFFAOYSA-N 2,3,5-trioxabicyclo[2.2.2]octane Chemical compound O1CC2CCC1OO2 FPEXZUSKGJEHCF-UHFFFAOYSA-N 0.000 description 2
YEWBOZCFGXOUQW-UHFFFAOYSA-N 2,6,7-trioxa-1-phosphabicyclo[2.2.2]octan-4-ylmethanol Chemical compound C1OP2OCC1(CO)CO2 YEWBOZCFGXOUQW-UHFFFAOYSA-N 0.000 description 2
BVUXDWXKPROUDO-UHFFFAOYSA-N 2,6-di-tert-butyl-4-ethylphenol Chemical compound CCC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 BVUXDWXKPROUDO-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
OEPOKWHJYJXUGD-UHFFFAOYSA-N 2-(3-phenylmethoxyphenyl)-1,3-thiazole-4-carbaldehyde Chemical compound O=CC1=CSC(C=2C=C(OCC=3C=CC=CC=3)C=CC=2)=N1 OEPOKWHJYJXUGD-UHFFFAOYSA-N 0.000 description 2
ZPIRWAHWDCHWLM-UHFFFAOYSA-N 2-dodecylsulfanylethanol Chemical compound CCCCCCCCCCCCSCCO ZPIRWAHWDCHWLM-UHFFFAOYSA-N 0.000 description 2
ODJQKYXPKWQWNK-UHFFFAOYSA-N 3,3'-Thiobispropanoic acid Chemical compound OC(=O)CCSCCC(O)=O ODJQKYXPKWQWNK-UHFFFAOYSA-N 0.000 description 2
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238000005809 transesterification reaction Methods 0.000 description 1
125000002889 tridecyl 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])[H] 0.000 description 1
IVIIAEVMQHEPAY-UHFFFAOYSA-N tridodecyl phosphite Chemical compound CCCCCCCCCCCCOP(OCCCCCCCCCCCC)OCCCCCCCCCCCC IVIIAEVMQHEPAY-UHFFFAOYSA-N 0.000 description 1
125000005591 trimellitate group Chemical group 0.000 description 1
CYTQBVOFDCPGCX-UHFFFAOYSA-N trimethyl phosphite Chemical compound COP(OC)OC CYTQBVOFDCPGCX-UHFFFAOYSA-N 0.000 description 1
125000003258 trimethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])[*:1] 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
229920001862 ultra low molecular weight polyethylene Polymers 0.000 description 1
229920006337 unsaturated polyester resin Polymers 0.000 description 1
150000003672 ureas Chemical class 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
210000003462 vein Anatomy 0.000 description 1
229920001866 very low density polyethylene Polymers 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
238000005303 weighing Methods 0.000 description 1
239000002023 wood Substances 0.000 description 1
150000003751 zinc Chemical class 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
239000004711 α-olefin Substances 0.000 description 1
239000002076 α-tocopherol Substances 0.000 description 1
235000004835 α-tocopherol Nutrition 0.000 description 1
235000007680 β-tocopherol Nutrition 0.000 description 1
239000011590 β-tocopherol Substances 0.000 description 1
239000002478 γ-tocopherol 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
QUEDXNHFTDJVIY-DQCZWYHMSA-N γ-tocopherol Chemical compound OC1=C(C)C(C)=C2O[C@@](CCC[C@H](C)CCC[C@H](C)CCCC(C)C)(C)CCC2=C1 QUEDXNHFTDJVIY-DQCZWYHMSA-N 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
- 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
- C08G73/00—Macromolecular compounds obtained by reactions forming a linkage containing nitrogen with or without oxygen or carbon in the main chain of the macromolecule, not provided for in groups C08G12/00 - C08G71/00
- C08G73/02—Polyamines
- C08G73/0273—Polyamines containing heterocyclic moieties in the main chain
- 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
- C08G73/00—Macromolecular compounds obtained by reactions forming a linkage containing nitrogen with or without oxygen or carbon in the main chain of the macromolecule, not provided for in groups C08G12/00 - C08G71/00
- C08G73/06—Polycondensates having nitrogen-containing heterocyclic rings in the main chain of the macromolecule
- C08G73/0622—Polycondensates containing six-membered rings, not condensed with other rings, with nitrogen atoms as the only ring hetero atoms
- C08G73/0638—Polycondensates containing six-membered rings, not condensed with other rings, with nitrogen atoms as the only ring hetero atoms with at least three nitrogen atoms in the ring
- C08G73/0644—Poly(1,3,5)triazines
- 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
- C08K5/16—Nitrogen-containing compounds
- C08K5/34—Heterocyclic compounds having nitrogen in the ring
- C08K5/3467—Heterocyclic compounds having nitrogen in the ring having more than two nitrogen atoms in the ring
- C08K5/3477—Six-membered rings
- C08K5/3492—Triazines
- C08K5/34926—Triazines also containing heterocyclic groups other than triazine groups

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Health & Medical Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Plural Heterocyclic Compounds (AREA)
Compositions Of Macromolecular Compounds (AREA)
Paper (AREA)
Hydrogenated Pyridines (AREA)

NL1009260A 1997-05-27 1998-05-26 Triazine-derivaten die 2,2,6,6-tetramethyl-4-piperidylgroepen bevatten. NL1009260C2 (nl)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
EP97810332		1997-05-27
EP97810332		1997-05-27

Publications (2)

Publication Number	Publication Date
NL1009260A1 NL1009260A1 (nl)	1998-12-01
NL1009260C2 true NL1009260C2 (nl)	1999-09-24

Family

ID=8230246

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NL1009260A NL1009260C2 (nl)	1997-05-27	1998-05-26	Triazine-derivaten die 2,2,6,6-tetramethyl-4-piperidylgroepen bevatten.

Country Status (12)

Country	Link
US (1)	US6114420A (fr)
JP (1)	JPH10330378A (fr)
KR (1)	KR19980087355A (fr)
BE (1)	BE1011937A3 (fr)
CA (1)	CA2238432A1 (fr)
DE (1)	DE19823282A1 (fr)
ES (1)	ES2138934B1 (fr)
FR (1)	FR2763949B1 (fr)
GB (1)	GB2325667B (fr)
IT (1)	ITMI981170A1 (fr)
NL (1)	NL1009260C2 (fr)
TW (1)	TW509683B (fr)

Families Citing this family (20)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
TW428008B (en) *	1997-05-27	2001-04-01	Ciba Sc Holding Ag	Block oligomers containing 1-hydrocarbyloxy-2,2,6,6-tetramethy1-4-piperidyl groups as stabilizers for organic materials
TW491872B (en) *	1997-05-27	2002-06-21	Ciba Sc Holding Ag	Block oligomers containing l-hydrocarbyloxy-2,2,6,6-tetramethyl-4- piperidyl groups as stabilizers for lower polyolefin
ES2213923T3 (es) *	1997-12-08	2004-09-01	Cytec Technology Corp.	Aminotriazinas protegidas por morfolino con sustituyentes amino impedidos y su uso como estabilizadores de luz.
US6271377B1 (en)	1999-02-25	2001-08-07	Ciba Specialty Chemicals Corporation	Hydroxy-substituted N-alkoxy hindered amines and compositions stabilized therewith
GB0003326D0 (en) *	1999-02-25	2000-04-05	Ciba Sc Holding Ag	Hydroxy-Substituted N-Alkoxy hindered amines
US6376584B1 (en)	1999-02-25	2002-04-23	Ciba Specialty Chemicals Corporation	Hydroxy-substituted N-alkoxy hindered amines and compositions stabilized therewith
US6392041B1 (en)	1999-02-25	2002-05-21	Ciba Specialty Chemicals Corporation	Hydroxy-substituted N-alkoxy hindered amines and compositions stabilized therewith
US7297735B2 (en) *	2003-03-05	2007-11-20	Eastman Chemical Company	Polycarbonate compositions
US7482397B2 (en) *	2003-01-13	2009-01-27	Eastman Chemical Company	Polycarbonate compositions
US20040143041A1 (en) *	2003-01-13	2004-07-22	Pearson Jason Clay	Polyester compositions
US20040192813A1 (en) *	2003-03-20	2004-09-30	Pearson Jason Clay	Polymer compositions containing an ultraviolet light absorbing compound
US7338992B2 (en) *	2003-03-05	2008-03-04	Eastman Chemical Company	Polyolefin compositions
US20040180994A1 (en) *	2003-03-05	2004-09-16	Pearson Jason Clay	Polyolefin compositions
US20050277713A1 (en) *	2003-03-05	2005-12-15	Pearson Jason C	Polymer blends
US20040183053A1 (en) *	2003-03-20	2004-09-23	Pearson Jason Clay	Process for the preparation of a hindered amine light stabilizer salt
KR101158123B1 (ko) *	2003-03-05	2012-06-19	이스트만 케미칼 컴파니	자외선 흡수 화합물을 함유하는 중합체 조성물
ATE390460T1 (de) *	2003-03-05	2008-04-15	Eastman Chem Co	Polymerblends
CA2788267A1 (fr) *	2010-03-09	2011-09-15	Basf Se	Polyamides resistant au vieillissement thermique
US10253164B2 (en) *	2014-05-15	2019-04-09	Basf Se	Highly effective stabilizer
EP2993216B1 (fr) *	2014-09-02	2017-07-26	Merck Patent GmbH	Composés et milieu liquide cristallin

Citations (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
EP0053775A2 (fr) *	1980-12-05	1982-06-16	Hoechst Aktiengesellschaft	Poly-bis-triazynylamines, procédé pour leur préparation, leur utilisation pour la stabilisation de polymères synthétiques et polymères ainsi stabilisés
US4459395A (en) *	1980-07-31	1984-07-10	Chimosa Chimica Organica S.P.A.	Piperidyl derivatives of triazine copolymers, processes for their preparation and stabilized composition containing these derivatives
EP0462069A2 (fr) *	1990-06-13	1991-12-18	Ciba-Geigy Ag	Nouveaux pipéridine-triazine co-oligomères et leur utilisation comme stabilisant pour des matériaux organiques

Family Cites Families (16)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
IT1052501B (it) *	1975-12-04	1981-07-20	Chimosa Chimica Organica Spa	Composti politriazinici utilizzabili per la stabilizzazione di polimeri sintetici e procedimento per la loro preparazione
US4234707A (en) *	1977-11-10	1980-11-18	Ciba-Geigy Corporation	Polymeric light stabilizers for plastics
DE2933078A1 (de) *	1979-08-16	1981-03-26	Hoechst Ag, 65929 Frankfurt	Neue triazinderivate, ihre herstellung und ihre verwendung als stabilisatoren fuer synthetische polymere
CA1134831A (fr) *	1980-02-04	1982-11-02	Carstab Corporation	Compose heterocyclique substitue 2,2,6,6- tetramethyle-4-piperidyle, et polymeres a base de ce compose
US4331586A (en) *	1981-07-20	1982-05-25	American Cyanamid Company	Novel light stabilizers for polymers
US4492791A (en) *	1982-05-04	1985-01-08	Ciba-Geigy Corporation	Process for the preparation of polyaminotriazines
US4526972A (en) *	1984-06-27	1985-07-02	Texaco Inc.	Ultraviolet light stabilizing sterically hindered polyoxyalkylene amines
JPS61176662A (ja) *	1985-02-01	1986-08-08	Adeka Argus Chem Co Ltd	安定化高分子材料組成物
US4847380A (en) *	1987-07-27	1989-07-11	Texaco Inc.	High molecular weight polyalkoxyamide, urea or urethane-containing piperidine radical
IT1227334B (it) *	1988-08-04	1991-04-08	Ciba Geigy Spa	Composti piperidin triazinici atti all'impiego come stabilizzanti per materiali organici.
CS270846B1 (en) *	1988-08-29	1990-08-14	Vass Frantisek	New polyaminotriazines and method of their preparation
CS273098B1 (en) *	1989-01-02	1991-03-12	Manasek Zdenek	Substituted polyaminotriazines and method of their preparation
IT1237129B (it) *	1989-11-10	1993-05-18	Valerio Borzatta	Composti piperidin-triazinici atti all'impiego come stabilizzanti per materiali organici.
US5112979A (en) *	1990-11-29	1992-05-12	Texaco Chemical Company	Polyoxyalkyleneamines containing tetraalkylpiperidine functionality and their use as light, heat and oxidation stabilizers
JP3183953B2 (ja) *	1992-07-07	2001-07-09	旭電化工業株式会社	安定化高分子材料組成物
IT1270975B (it) *	1993-06-03	1997-05-26	Ciba Geigy Spa	Composti piperidin-triazinici atti all'impiego come stabilizzanti allaluce, al calore e alla ossidazione per materiali organici

1998
- 1998-05-04 TW TW087106882A patent/TW509683B/zh not_active IP Right Cessation
- 1998-05-19 GB GB9810645A patent/GB2325667B/en not_active Expired - Fee Related
- 1998-05-25 CA CA002238432A patent/CA2238432A1/fr not_active Abandoned
- 1998-05-25 DE DE19823282A patent/DE19823282A1/de not_active Withdrawn
- 1998-05-26 NL NL1009260A patent/NL1009260C2/nl not_active IP Right Cessation
- 1998-05-26 IT IT98MI001170A patent/ITMI981170A1/it unknown
- 1998-05-26 ES ES009801082A patent/ES2138934B1/es not_active Expired - Fee Related
- 1998-05-26 FR FR9806584A patent/FR2763949B1/fr not_active Expired - Fee Related
- 1998-05-26 KR KR1019980018947A patent/KR19980087355A/ko not_active Ceased
- 1998-05-26 US US09/084,681 patent/US6114420A/en not_active Expired - Fee Related
- 1998-05-27 JP JP10162979A patent/JPH10330378A/ja active Pending
- 1998-05-27 BE BE9800405A patent/BE1011937A3/fr not_active IP Right Cessation

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4459395A (en) *	1980-07-31	1984-07-10	Chimosa Chimica Organica S.P.A.	Piperidyl derivatives of triazine copolymers, processes for their preparation and stabilized composition containing these derivatives
EP0053775A2 (fr) *	1980-12-05	1982-06-16	Hoechst Aktiengesellschaft	Poly-bis-triazynylamines, procédé pour leur préparation, leur utilisation pour la stabilisation de polymères synthétiques et polymères ainsi stabilisés
EP0462069A2 (fr) *	1990-06-13	1991-12-18	Ciba-Geigy Ag	Nouveaux pipéridine-triazine co-oligomères et leur utilisation comme stabilisant pour des matériaux organiques

Also Published As

Publication number	Publication date
JPH10330378A (ja)	1998-12-15
KR19980087355A (ko)	1998-12-05
ES2138934B1 (es)	2000-09-16
GB9810645D0 (en)	1998-07-15
ITMI981170A1 (it)	1999-11-26
BE1011937A3 (fr)	2000-03-07
ES2138934A1 (es)	2000-01-16
FR2763949B1 (fr)	2000-05-12
TW509683B (en)	2002-11-11
FR2763949A1 (fr)	1998-12-04
DE19823282A1 (de)	1998-12-03
NL1009260A1 (nl)	1998-12-01
GB2325667A (en)	1998-12-02
GB2325667B (en)	2001-04-18
CA2238432A1 (fr)	1998-11-27
US6114420A (en)	2000-09-05

Legal Events

Date	Code	Title	Description
1999-02-01	AD1A	A request for search or an international type search has been filed
1999-12-01	PD2B	A search report has been drawn up
2005-02-01	VD1	Lapsed due to non-payment of the annual fee	Effective date: 20041201

Publication	Publication Date	Title
NL1012844C2 (nl)	2000-12-06	Draaginrichting voor een adembeschermingsapparaat.
US6020406A (en)	2000-02-01	Synergistic stabilizer mixture
CA2167660C (fr)	2007-06-19	Melange stabilisateur synergiste
US5817821A (en)	1998-10-06	Mixtures of polyalkylpiperidin-4-yl dicarboxylic acid esters as stabilizers for organic materials
JPH09216946A (ja)	1997-08-19	有機材料の安定剤としての２，２，６，６−テトラメチルピペリジル基を含有するブロックオリゴマー
US6114420A (en)	2000-09-05	Triazine derivatives containing 2,2,6,6-tetramethyl-4-piperidyl groups
US5837792A (en)	1998-11-17	Polysiloxane light stabilizers
US5919399A (en)	1999-07-06	Synergistic stabilizer mixture
US5561179A (en)	1996-10-01	Piperidine compounds containing silane groups as stabilizers for organic materials
SK278485B6 (en)	1997-07-09	The piperidine compound containing silane groups, a stabilised synthetic polymeric material with its content and a method of stabilisation of this material
NL9401175A (nl)	1995-02-16	Nieuwe derivaten van 2,2,6,6-tetramethyl-4-piperidinol voor toepassing als stabiliseermiddelen tegen licht, hitte en oxidatie voor organische materialen.
NL9400374A (nl)	1994-10-03	Nieuwe polymethylpiperidine-verbindingen die silaan-groepen bevatten en die bruikbaar zijn als stabiliseermiddelen voor organische materialen.
FR2809739A1 (fr)	2001-12-07	Melanges de stabilisants
NL1001605C2 (nl)	1997-04-03	Nieuwe 2,2,6,6-tetramethylpiperidine-derivaten voor toepassing als sta- biliseermiddelen voor organische materialen tegen licht, hitte en oxida- tie.
NL1013844C2 (nl)	2001-11-29	Sterisch gehinderde amineverbindingen.
JPH0770064A (ja)	1995-03-14	有機材料用の安定剤としての用途のための新規ポリアルキル−４−ピペリジノール誘導体
EP0984958B1 (fr)	2003-03-26	Blocs oligomeres contenant des groupes 1-hydrocarbyloxy-2,2,6,6-tetramethyl-4-piperidyl comme stabilisants pour des materiaux organiques
US5847132A (en)	1998-12-08	Polytriazine derivatives containing polyalkylpiperidinyloxy or polyalkylpiperidinylamino groups
EP0794972B1 (fr)	1999-01-13	Composes piperidines contenant des groupes silanes en tant que stabilisateurs de materiaux organiques
NL1001781C2 (nl)	1997-03-25	Silaangroepen bevattende piperidine-triazine-verbindingen als stabiliseermiddelen voor organische materialen.
WO2005090307A1 (fr)	2005-09-29	Synthese d'ethers amines
NL9400515A (nl)	1994-11-01	Nieuwe piperidine-triazine-verbindingen die geschikt zijn voor gebruik als stabiliseermiddelen voor organische materialen.
NL9400213A (nl)	1994-09-01	Nieuwe piperidine-triazine-verbindingen die geschikt zijn voor gebruik als stabiliseermiddelen voor organische materialen.
EP1185577B1 (fr)	2003-05-21	Stabilisateurs polysilane contenant de groupes amide a encombrement sterique
EP0835873A1 (fr)	1998-04-15	Mélanges de composés de tétramines de polyalkylpiperidinylaminotriazine trisubstitués et tétrasubstitués