SK321090A3 - 2,4-dimethyl-6-sec.alkyl-phenols, and stabilised organic materials them containing - Google Patents

2,4-dimethyl-6-sec.alkyl-phenols, and stabilised organic materials them containing Download PDF

Info

Publication number: SK321090A3
Authority: SK; Slovakia
Prior art keywords: mixture; styrene; formula; tert; compound
Prior art date: 1989-06-30

Application number

SK3210-90A

Other languages

English (en)

Slovak (sk)

Other versions

SK279627B6 (sk

Inventor

Rita Pitteloud

Paul Dubs

Original Assignee

Ciba Geigy 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.)

1989-06-30

Filing date

1990-06-27

Publication date

1999-01-11

1990-06-27 Application filed by Ciba Geigy Ag filed Critical Ciba Geigy Ag

1999-01-11 Publication of SK279627B6 publication Critical patent/SK279627B6/sk

1999-01-11 Publication of SK321090A3 publication Critical patent/SK321090A3/sk

Links

239000011368 organic material Substances 0.000 title claims description 12
239000000203 mixture Substances 0.000 claims description 90
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 72
-1 copolyamide Polymers 0.000 claims description 53
150000001875 compounds Chemical class 0.000 claims description 49
229920001577 copolymer Polymers 0.000 claims description 46
KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 claims description 27
125000000217 alkyl group Chemical group 0.000 claims description 20
239000004952 Polyamide Substances 0.000 claims description 14
229920002647 polyamide Polymers 0.000 claims description 14
229920001897 terpolymer Polymers 0.000 claims description 14
NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 claims description 13
239000004793 Polystyrene Substances 0.000 claims description 12
229920002223 polystyrene Polymers 0.000 claims description 12
229920006324 polyoxymethylene Polymers 0.000 claims description 11
238000000034 method Methods 0.000 claims description 10
239000004417 polycarbonate Substances 0.000 claims description 9
239000004721 Polyphenylene oxide Substances 0.000 claims description 8
229920000728 polyester Polymers 0.000 claims description 8
239000004814 polyurethane Substances 0.000 claims description 8
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 7
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 7
229920006380 polyphenylene oxide Polymers 0.000 claims description 7
125000004432 carbon atom Chemical group C* 0.000 claims description 6
229920002635 polyurethane Polymers 0.000 claims description 6
229920000515 polycarbonate Polymers 0.000 claims description 5
BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 claims description 4
VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 claims description 4
229930182556 Polyacetal Natural products 0.000 claims description 4
230000015556 catabolic process Effects 0.000 claims description 4
238000006731 degradation reaction Methods 0.000 claims description 4
239000000463 material Substances 0.000 claims description 4
230000003647 oxidation Effects 0.000 claims description 4
238000007254 oxidation reaction Methods 0.000 claims description 4
230000000087 stabilizing effect Effects 0.000 claims description 4
230000005855 radiation Effects 0.000 claims description 3
150000003440 styrenes Chemical class 0.000 claims description 3
239000008187 granular material Substances 0.000 claims 1
238000010525 oxidative degradation reaction Methods 0.000 claims 1
239000011145 styrene acrylonitrile resin Substances 0.000 claims 1
229920000642 polymer Polymers 0.000 description 17
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 12
239000005977 Ethylene Substances 0.000 description 12
229910052757 nitrogen Inorganic materials 0.000 description 12
MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 11
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 9
239000003054 catalyst Substances 0.000 description 9
150000002148 esters Chemical class 0.000 description 9
238000002360 preparation method Methods 0.000 description 9
GHKOFFNLGXMVNJ-UHFFFAOYSA-N Didodecyl thiobispropanoate Chemical compound CCCCCCCCCCCCOC(=O)CCSCCC(=O)OCCCCCCCCCCCC GHKOFFNLGXMVNJ-UHFFFAOYSA-N 0.000 description 8
239000004743 Polypropylene Substances 0.000 description 8
239000000839 emulsion Substances 0.000 description 8
229920002857 polybutadiene Polymers 0.000 description 8
KUFFULVDNCHOFZ-UHFFFAOYSA-N 2,4-xylenol Chemical compound CC1=CC=C(O)C(C)=C1 KUFFULVDNCHOFZ-UHFFFAOYSA-N 0.000 description 7
239000005062 Polybutadiene Substances 0.000 description 7
239000000654 additive Substances 0.000 description 7
238000004587 chromatography analysis Methods 0.000 description 7
150000001993 dienes Chemical class 0.000 description 7
229920001684 low density polyethylene Polymers 0.000 description 7
GQEZCXVZFLOKMC-UHFFFAOYSA-N 1-hexadecene Chemical compound CCCCCCCCCCCCCCC=C GQEZCXVZFLOKMC-UHFFFAOYSA-N 0.000 description 6
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 6
PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 6
239000004698 Polyethylene Substances 0.000 description 6
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 6
238000006243 chemical reaction Methods 0.000 description 6
239000004702 low-density polyethylene Substances 0.000 description 6
GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 description 6
229920000573 polyethylene Polymers 0.000 description 6
239000004800 polyvinyl chloride Substances 0.000 description 6
229920000915 polyvinyl chloride Polymers 0.000 description 6
239000000047 product Substances 0.000 description 6
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 5
229920001903 high density polyethylene Polymers 0.000 description 5
239000004700 high-density polyethylene Substances 0.000 description 5
SYSQUGFVNFXIIT-UHFFFAOYSA-N n-[4-(1,3-benzoxazol-2-yl)phenyl]-4-nitrobenzenesulfonamide Chemical class C1=CC([N+](=O)[O-])=CC=C1S(=O)(=O)NC1=CC=C(C=2OC3=CC=CC=C3N=2)C=C1 SYSQUGFVNFXIIT-UHFFFAOYSA-N 0.000 description 5
150000002989 phenols Chemical class 0.000 description 5
229920005989 resin Polymers 0.000 description 5
239000011347 resin Substances 0.000 description 5
125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 5
229920002554 vinyl polymer Polymers 0.000 description 5
239000001993 wax Substances 0.000 description 5
VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 4
TVWGHFVGFWIHFN-UHFFFAOYSA-N 2-hexadecan-2-yl-4,6-dimethylphenol Chemical compound CCCCCCCCCCCCCCC(C)C1=CC(C)=CC(C)=C1O TVWGHFVGFWIHFN-UHFFFAOYSA-N 0.000 description 4
GAWIXWVDTYZWAW-UHFFFAOYSA-N C[CH]O Chemical group C[CH]O GAWIXWVDTYZWAW-UHFFFAOYSA-N 0.000 description 4
229920000877 Melamine resin Polymers 0.000 description 4
150000001252 acrylic acid derivatives Chemical class 0.000 description 4
239000003795 chemical substances by application Substances 0.000 description 4
239000007788 liquid Substances 0.000 description 4
239000003921 oil Substances 0.000 description 4
229920000570 polyether Polymers 0.000 description 4
229920001155 polypropylene Polymers 0.000 description 4
239000011541 reaction mixture Substances 0.000 description 4
230000006641 stabilisation Effects 0.000 description 4
238000011105 stabilization Methods 0.000 description 4
150000005846 sugar alcohols Polymers 0.000 description 4
239000004711 α-olefin Substances 0.000 description 4
SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 3
NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 3
PNEYBMLMFCGWSK-UHFFFAOYSA-N Alumina Chemical compound [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 3
NLZUEZXRPGMBCV-UHFFFAOYSA-N Butylhydroxytoluene Chemical compound CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 NLZUEZXRPGMBCV-UHFFFAOYSA-N 0.000 description 3
229920002943 EPDM rubber Polymers 0.000 description 3
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 3
229920002396 Polyurea Polymers 0.000 description 3
XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 3
239000002253 acid Substances 0.000 description 3
150000001412 amines Chemical class 0.000 description 3
238000009835 boiling Methods 0.000 description 3
235000010354 butylated hydroxytoluene Nutrition 0.000 description 3
150000001991 dicarboxylic acids Chemical class 0.000 description 3
229920001971 elastomer Polymers 0.000 description 3
238000000921 elemental analysis Methods 0.000 description 3
150000002170 ethers Chemical class 0.000 description 3
229910052736 halogen Inorganic materials 0.000 description 3
150000002367 halogens Chemical class 0.000 description 3
XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 description 3
229920000126 latex Polymers 0.000 description 3
229920000092 linear low density polyethylene Polymers 0.000 description 3
239000004707 linear low-density polyethylene Substances 0.000 description 3
239000002480 mineral oil Substances 0.000 description 3
239000000178 monomer Substances 0.000 description 3
VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 3
229940117969 neopentyl glycol Drugs 0.000 description 3
229910052759 nickel Inorganic materials 0.000 description 3
235000019198 oils Nutrition 0.000 description 3
ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 3
239000000843 powder Substances 0.000 description 3
QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 3
125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 3
239000000376 reactant Substances 0.000 description 3
239000002904 solvent Substances 0.000 description 3
238000003756 stirring Methods 0.000 description 3
YODZTKMDCQEPHD-UHFFFAOYSA-N thiodiglycol Chemical compound OCCSCCO YODZTKMDCQEPHD-UHFFFAOYSA-N 0.000 description 3
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 3
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
JUSNISPZXDHWQK-UHFFFAOYSA-N 2,4-dimethyl-6-octadecan-2-ylphenol Chemical compound CCCCCCCCCCCCCCCCC(C)C1=CC(C)=CC(C)=C1O JUSNISPZXDHWQK-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
GZRFMZUFEYOIML-UHFFFAOYSA-N 2-(2-ethyltetradecyl)-4,6-dimethylphenol Chemical compound CCCCCCCCCCCCC(CC)CC1=CC(C)=CC(C)=C1O GZRFMZUFEYOIML-UHFFFAOYSA-N 0.000 description 2
KPPISGHNOYPYCJ-UHFFFAOYSA-N 2-dodecan-2-yl-4,6-dimethylphenol Chemical compound CCCCCCCCCCC(C)C1=CC(C)=CC(C)=C1O KPPISGHNOYPYCJ-UHFFFAOYSA-N 0.000 description 2
ZKUAZHHEOVSSDB-UHFFFAOYSA-N 2-dodecan-3-yl-4,6-dimethylphenol Chemical compound CCCCCCCCCC(CC)C1=CC(C)=CC(C)=C1O ZKUAZHHEOVSSDB-UHFFFAOYSA-N 0.000 description 2
WPMYUUITDBHVQZ-UHFFFAOYSA-N 3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoic acid Chemical compound CC(C)(C)C1=CC(CCC(O)=O)=CC(C(C)(C)C)=C1O WPMYUUITDBHVQZ-UHFFFAOYSA-N 0.000 description 2
VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 2
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 2
PEEHTFAAVSWFBL-UHFFFAOYSA-N Maleimide Chemical compound O=C1NC(=O)C=C1 PEEHTFAAVSWFBL-UHFFFAOYSA-N 0.000 description 2
229920002292 Nylon 6 Polymers 0.000 description 2
YIKSCQDJHCMVMK-UHFFFAOYSA-N Oxamide Chemical class NC(=O)C(N)=O YIKSCQDJHCMVMK-UHFFFAOYSA-N 0.000 description 2
229920002367 Polyisobutene Polymers 0.000 description 2
235000021355 Stearic acid Nutrition 0.000 description 2
QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 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
GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
229920001807 Urea-formaldehyde Polymers 0.000 description 2
BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 2
229920000800 acrylic rubber Polymers 0.000 description 2
230000000996 additive effect Effects 0.000 description 2
239000001361 adipic acid Substances 0.000 description 2
235000011037 adipic acid Nutrition 0.000 description 2
229920000180 alkyd Polymers 0.000 description 2
125000005250 alkyl acrylate group Chemical group 0.000 description 2
XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 description 2
239000003963 antioxidant agent Substances 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
229920001400 block copolymer Polymers 0.000 description 2
229910052799 carbon Inorganic materials 0.000 description 2
239000007859 condensation product Substances 0.000 description 2
238000001816 cooling Methods 0.000 description 2
LPIQUOYDBNQMRZ-UHFFFAOYSA-N cyclopentene Chemical compound C1CC=CC1 LPIQUOYDBNQMRZ-UHFFFAOYSA-N 0.000 description 2
125000002704 decyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
150000004985 diamines Chemical class 0.000 description 2
238000001035 drying Methods 0.000 description 2
239000000806 elastomer Substances 0.000 description 2
239000003822 epoxy resin Substances 0.000 description 2
238000004817 gas chromatography Methods 0.000 description 2
230000005484 gravity Effects 0.000 description 2
LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 2
NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 description 2
229920005669 high impact polystyrene Polymers 0.000 description 2
238000004128 high performance liquid chromatography Methods 0.000 description 2
239000004797 high-impact polystyrene Substances 0.000 description 2
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 2
239000004615 ingredient Substances 0.000 description 2
229920000554 ionomer Polymers 0.000 description 2
ZFSLODLOARCGLH-UHFFFAOYSA-N isocyanuric acid Chemical compound OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 0.000 description 2
QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 2
239000004816 latex Substances 0.000 description 2
239000003446 ligand Substances 0.000 description 2
IVSZLXZYQVIEFR-UHFFFAOYSA-N m-xylene Chemical group CC1=CC=CC(C)=C1 IVSZLXZYQVIEFR-UHFFFAOYSA-N 0.000 description 2
FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 2
JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 2
239000000155 melt Substances 0.000 description 2
238000002844 melting Methods 0.000 description 2
230000008018 melting Effects 0.000 description 2
150000004702 methyl esters Chemical class 0.000 description 2
ZGEGCLOFRBLKSE-UHFFFAOYSA-N methylene hexane Natural products CCCCCC=C ZGEGCLOFRBLKSE-UHFFFAOYSA-N 0.000 description 2
238000012986 modification Methods 0.000 description 2
230000004048 modification Effects 0.000 description 2
150000005673 monoalkenes Chemical class 0.000 description 2
125000001421 myristyl 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])[H] 0.000 description 2
229920003052 natural elastomer Polymers 0.000 description 2
229920001194 natural rubber Polymers 0.000 description 2
QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 2
OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 2
125000000913 palmityl 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])[H] 0.000 description 2
WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 2
ZQBAKBUEJOMQEX-UHFFFAOYSA-N phenyl salicylate Chemical compound OC1=CC=CC=C1C(=O)OC1=CC=CC=C1 ZQBAKBUEJOMQEX-UHFFFAOYSA-N 0.000 description 2
239000000049 pigment Substances 0.000 description 2
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238000006116 polymerization reaction Methods 0.000 description 2
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BBEAQIROQSPTKN-UHFFFAOYSA-N pyrene Chemical compound C1=CC=C2C=CC3=CC=CC4=CC=C1C2=C43 BBEAQIROQSPTKN-UHFFFAOYSA-N 0.000 description 2
239000007787 solid Substances 0.000 description 2
238000009987 spinning Methods 0.000 description 2
239000003381 stabilizer Substances 0.000 description 2
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KKEYFWRCBNTPAC-UHFFFAOYSA-L terephthalate(2-) Chemical compound [O-]C(=O)C1=CC=C(C([O-])=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-L 0.000 description 2
238000012360 testing method Methods 0.000 description 2
JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 2
HVLLSGMXQDNUAL-UHFFFAOYSA-N triphenyl phosphite Chemical compound C=1C=CC=CC=1OP(OC=1C=CC=CC=1)OC1=CC=CC=C1 HVLLSGMXQDNUAL-UHFFFAOYSA-N 0.000 description 2
RSJKGSCJYJTIGS-UHFFFAOYSA-N undecane Chemical compound CCCCCCCCCCC RSJKGSCJYJTIGS-UHFFFAOYSA-N 0.000 description 2
239000010457 zeolite Substances 0.000 description 2
OUBISKKOUYNDML-UHFFFAOYSA-N (2,2,6,6-tetramethylpiperidin-4-yl) 2-[bis[2-oxo-2-(2,2,6,6-tetramethylpiperidin-4-yl)oxyethyl]amino]acetate Chemical compound C1C(C)(C)NC(C)(C)CC1OC(=O)CN(CC(=O)OC1CC(C)(C)NC(C)(C)C1)CC(=O)OC1CC(C)(C)NC(C)(C)C1 OUBISKKOUYNDML-UHFFFAOYSA-N 0.000 description 1
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229920001195 polyisoprene Polymers 0.000 description 1
229920000193 polymethacrylate Polymers 0.000 description 1
229920000098 polyolefin Polymers 0.000 description 1
229920000069 polyphenylene sulfide Polymers 0.000 description 1
229920002689 polyvinyl acetate Polymers 0.000 description 1
239000011118 polyvinyl acetate Substances 0.000 description 1
229920002451 polyvinyl alcohol Polymers 0.000 description 1
229920002620 polyvinyl fluoride Polymers 0.000 description 1
239000005033 polyvinylidene chloride Substances 0.000 description 1
229920002981 polyvinylidene fluoride Polymers 0.000 description 1
229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
239000001267 polyvinylpyrrolidone Substances 0.000 description 1
235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 description 1
238000012545 processing Methods 0.000 description 1
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
239000011814 protection agent Substances 0.000 description 1
229910052895 riebeckite Inorganic materials 0.000 description 1
239000005060 rubber Substances 0.000 description 1
150000003839 salts Chemical class 0.000 description 1
229920006395 saturated elastomer Polymers 0.000 description 1
239000000565 sealant Substances 0.000 description 1
150000004760 silicates Chemical class 0.000 description 1
IJRHDFLHUATAOS-DPMBMXLASA-M sodium ricinoleate Chemical compound [Na+].CCCCCC[C@@H](O)C\C=C/CCCCCCCC([O-])=O IJRHDFLHUATAOS-DPMBMXLASA-M 0.000 description 1
238000001228 spectrum Methods 0.000 description 1
239000007858 starting material Substances 0.000 description 1
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 1
238000005728 strengthening Methods 0.000 description 1
229920000638 styrene acrylonitrile Polymers 0.000 description 1
229920003048 styrene butadiene rubber Polymers 0.000 description 1
238000006467 substitution reaction Methods 0.000 description 1
229920003051 synthetic elastomer Polymers 0.000 description 1
239000005061 synthetic rubber Substances 0.000 description 1
239000000454 talc Substances 0.000 description 1
229910052623 talc Inorganic materials 0.000 description 1
MHSKRLJMQQNJNC-UHFFFAOYSA-N terephthalamide Chemical compound NC(=O)C1=CC=C(C(N)=O)C=C1 MHSKRLJMQQNJNC-UHFFFAOYSA-N 0.000 description 1
238000002076 thermal analysis method Methods 0.000 description 1
229920001169 thermoplastic Polymers 0.000 description 1
229920002803 thermoplastic polyurethane Polymers 0.000 description 1
239000004416 thermosoftening plastic Substances 0.000 description 1
239000004408 titanium dioxide Substances 0.000 description 1
VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 1
125000002469 tricosyl 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])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 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
ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1
125000005591 trimellitate group Chemical group 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
150000003672 ureas Chemical class 0.000 description 1
235000015112 vegetable and seed oil Nutrition 0.000 description 1
235000019871 vegetable fat Nutrition 0.000 description 1
150000003739 xylenols Chemical class 0.000 description 1
238000004383 yellowing Methods 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

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C39/00—Compounds having at least one hydroxy or O-metal group bound to a carbon atom of a six-membered aromatic ring
- C07C39/02—Compounds having at least one hydroxy or O-metal group bound to a carbon atom of a six-membered aromatic ring monocyclic with no unsaturation outside the aromatic ring
- C07C39/06—Alkylated phenols
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C37/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom of a six-membered aromatic ring
- C07C37/11—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom of a six-membered aromatic ring by reactions increasing the number of carbon atoms
- C07C37/20—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom of a six-membered aromatic ring by reactions increasing the number of carbon atoms using aldehydes or ketones
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C37/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom of a six-membered aromatic ring
- C07C37/50—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom of a six-membered aromatic ring by reactions decreasing the number of carbon atoms
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C37/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom of a six-membered aromatic ring
- C07C37/68—Purification; separation; Use of additives, e.g. for stabilisation
- C07C37/70—Purification; separation; Use of additives, e.g. for stabilisation by physical treatment
- C07C37/74—Purification; separation; Use of additives, e.g. for stabilisation by physical treatment by distillation
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C37/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom of a six-membered aromatic ring
- C07C37/68—Purification; separation; Use of additives, e.g. for stabilisation
- C07C37/70—Purification; separation; Use of additives, e.g. for stabilisation by physical treatment
- C07C37/84—Purification; separation; Use of additives, e.g. for stabilisation by physical treatment by crystallisation
- 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
- C08K5/13—Phenols; Phenolates
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K15/00—Anti-oxidant compositions; Compositions inhibiting chemical change
- C09K15/04—Anti-oxidant compositions; Compositions inhibiting chemical change containing organic compounds
- C09K15/06—Anti-oxidant compositions; Compositions inhibiting chemical change containing organic compounds containing oxygen
- C09K15/08—Anti-oxidant compositions; Compositions inhibiting chemical change containing organic compounds containing oxygen containing a phenol or quinone moiety
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/52—Improvements relating to the production of bulk chemicals using catalysts, e.g. selective catalysts

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Chemical Kinetics & Catalysis (AREA)
Health & Medical Sciences (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Crystallography & Structural Chemistry (AREA)
Engineering & Computer Science (AREA)
Materials Engineering (AREA)
Compositions Of Macromolecular Compounds (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Anti-Oxidant Or Stabilizer Compositions (AREA)

SK3210-90A 1989-06-30 1990-06-27 2,4-dimethyl-6-sec.alkyl-phenols, and stabilised organic materials them containing SK321090A3 (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
CH243589		1989-06-30

Publications (2)

Publication Number	Publication Date
SK279627B6 SK279627B6 (sk)	1999-01-11
SK321090A3 true SK321090A3 (en)	1999-01-11

Family

ID=4233737

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
SK3210-90A SK321090A3 (en)	1989-06-30	1990-06-27	2,4-dimethyl-6-sec.alkyl-phenols, and stabilised organic materials them containing

Country Status (13)

Country	Link
US (1)	US5098945A (cs)
EP (1)	EP0406169B1 (cs)
JP (1)	JP2923674B2 (cs)
KR (1)	KR0168044B1 (cs)
CN (2)	CN1054143C (cs)
BR (1)	BR9003097A (cs)
CA (1)	CA2020051C (cs)
CZ (1)	CZ285993B6 (cs)
DD (1)	DD298945A5 (cs)
DE (1)	DE59010722D1 (cs)
ES (1)	ES2103732T3 (cs)
RU (2)	RU2068424C1 (cs)
SK (1)	SK321090A3 (cs)

Families Citing this family (14)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
ES2101994T3 (es) *	1992-04-08	1997-07-16	Ciba Geigy Ag	Antioxidantes liquidos como estabilizadores.
TW276260B (cs) *	1992-07-15	1996-05-21	Ciba Geigy Ag
DE4226288A1 (de) *	1992-08-08	1994-02-10	Hoechst Ag	Verfahren zur thermooxidativen Stabilisierung von Oxalkylenglykolalkylethern und thermooxidativ stabilisierte Mischungen von Oxalkylenglykolalkylethern
FR2696471B1 (fr) *	1992-10-02	1994-12-23	Inst Textile De France	Utilisation de la vanilline et de ses dérivés comme agents de protection anti-UV.
US5958254A (en) *	1992-11-24	1999-09-28	Commonwealth Scientific And Industrial Research Organization	Oxygen scavengers independent of transition metal catalysts
EP0669367A1 (de) *	1994-02-24	1995-08-30	Ciba-Geigy Ag	Phenolische Stabilisatormischungen
MY113152A (en) *	1996-01-31	2001-11-30	Ciba Holding Inc	Synergistic mixture consisting of a 2-4-dimethyl-6-s-alkylphenol and a sterically hindered phenol
ES2137101B1 (es) *	1997-01-30	2000-11-01	Ciba Sc Holding Ag	Mezcla sinergistica que consiste en un 2,4-dimetil-6-s-alquilfenol y un fenol estericamente impedido.
JP3802999B2 (ja) *	1999-08-09	2006-08-02	信越化学工業株式会社	塩化ビニル系重合体の製造方法
US6538056B1 (en)	2000-10-10	2003-03-25	Clariant International Ltd.	Polyolefin articles with long-term elevated temperature stability
RU2184124C1 (ru) *	2000-11-28	2002-06-27	Открытое акционерное общество "Нижнекамскнефтехим"	Способ стабилизации бутилкаучука
CN104591970B (zh) *	2014-12-23	2016-06-15	天津利安隆新材料股份有限公司	2,4-二甲基-6-（1-甲基-十五烷基）苯酚的制备方法
ES2765411T3 (es)	2016-01-21	2020-06-09	Basf Se	Mezcla de aditivos para la estabilización de poliol y poliuretano
CN107602353A (zh) *	2017-11-14	2018-01-19	郑程	一种防老剂264的制备方法

Family Cites Families (16)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US2198349A (en) *	1932-10-10	1940-04-23	Sharp & Dohme Inc	Alkyl cresols
US2073995A (en) *	1934-06-22	1937-03-16	Abbott Lab	Alkyl cresols
US2205947A (en) *	1935-09-25	1940-06-25	Nat Aniline & Chem Co Inc	Nuclear alkyl derivatives of phenol compounds
US2202877A (en) *	1937-04-12	1940-06-04	Gulf Oil Corp	Antioxidants and petroleum oils containing the same
US2605251A (en) *	1946-03-09	1952-07-29	Firestone Tire & Rubber Co	Butadiene rubbery copolymer stabilized with 2, 4-dimethyl-6-octylphenol
US3082258A (en) *	1960-05-12	1963-03-19	Eastman Kodak Co	Alkylation of phenols
DE1142873B (de) *	1961-01-25	1963-01-31	Bayer Ag	Verfahren zur Herstellung von 2- und bzw. oder 6-Alkylphenolen
US3367981A (en) *	1963-05-10	1968-02-06	Ethyl Corp	Phenol alkylation process
US3347938A (en) *	1964-04-23	1967-10-17	Eastman Kodak Co	Antioxidant composition
US3511802A (en) *	1968-06-10	1970-05-12	Eastman Kodak Co	Stabilized polypropylene resin composition
US3929912A (en) *	1970-05-25	1975-12-30	Universal Oil Prod Co	Alkylation of hydroxy-substituted aromatic compounds
US4086283A (en) *	1975-06-25	1978-04-25	Bayer Aktiengesellschaft	Process for preparing thymol
US4405818A (en) *	1981-09-30	1983-09-20	Mobil Oil Corporation	Production of meta-isopropylphenolic products
SU1182020A1 (ru) *	1983-07-08	1985-09-30	Отделение Нефтехимии Института Физико-Органической Химии И Углехимии Ан Усср	Способ получени 2-(1-метилалкил)-фенолов
US4954663A (en) *	1988-10-06	1990-09-04	Mobil Oil Corp.	Process for preparing long chain alkyl phenols
CA1326095C (en) *	1987-05-18	1994-01-11	Toshikazu Ijitsu	Styrene-based resin composition and moldings produced from said composition

1990
- 1990-06-21 ES ES90810463T patent/ES2103732T3/es not_active Expired - Lifetime
- 1990-06-21 DE DE59010722T patent/DE59010722D1/de not_active Expired - Lifetime
- 1990-06-21 EP EP90810463A patent/EP0406169B1/de not_active Expired - Lifetime
- 1990-06-27 CZ CS903210A patent/CZ285993B6/cs not_active IP Right Cessation
- 1990-06-27 SK SK3210-90A patent/SK321090A3/sk not_active IP Right Cessation
- 1990-06-28 CA CA002020051A patent/CA2020051C/en not_active Expired - Lifetime
- 1990-06-28 DD DD90342260A patent/DD298945A5/de not_active IP Right Cessation
- 1990-06-28 KR KR1019900009596A patent/KR0168044B1/ko not_active Expired - Lifetime
- 1990-06-29 JP JP2172536A patent/JP2923674B2/ja not_active Expired - Lifetime
- 1990-06-29 RU SU904830348A patent/RU2068424C1/ru active
- 1990-06-30 CN CN90106526A patent/CN1054143C/zh not_active Expired - Lifetime
- 1990-07-02 BR BR909003097A patent/BR9003097A/pt not_active IP Right Cessation
1991
- 1991-02-11 US US07/654,415 patent/US5098945A/en not_active Expired - Lifetime
1992
- 1992-07-24 RU SU925052443A patent/RU2067972C1/ru active
1999
- 1999-01-29 CN CN99101817A patent/CN1090167C/zh not_active Expired - Lifetime

Also Published As

Publication number	Publication date
CN1048865A (zh)	1991-01-30
RU2068424C1 (ru)	1996-10-27
CZ321090A3 (cs)	1999-08-11
SK279627B6 (sk)	1999-01-11
CN1054143C (zh)	2000-07-05
JPH0350247A (ja)	1991-03-04
KR910000939A (ko)	1991-01-30
HK1003005A1 (en)	1998-09-30
EP0406169B1 (de)	1997-06-04
DE59010722D1 (de)	1997-07-10
BR9003097A (pt)	1991-08-27
ES2103732T3 (es)	1997-10-01
CZ285993B6 (cs)	1999-12-15
RU2067972C1 (ru)	1996-10-20
KR0168044B1 (ko)	1999-03-20
DD298945A5 (de)	1992-03-19
US5098945A (en)	1992-03-24
EP0406169A1 (de)	1991-01-02
JP2923674B2 (ja)	1999-07-26
CA2020051A1 (en)	1990-12-31
CN1229783A (zh)	1999-09-29
CA2020051C (en)	2001-11-20
CN1090167C (zh)	2002-09-04

Legal Events

Date	Code	Title	Description
2010-08-09	MK4A	Expiry of patent	Expiry date: 20100627

Publication	Publication Date	Title
RU2130931C1 (ru)	1999-05-27	Производные бензофуран-2-онов, стабилизированная композиция, способ стабилизации, производные миндальной кислоты и способ их получения
EP0415887B1 (de)	1994-10-05	3-Phenylbenzofuran-2-one
CZ290103B6 (cs)	2002-05-15	3-(Karboxymethoxyfenyl)benzofuran-2-on, kompozicetuto sloučeninu obsahující, použití této sloučeniny jako stabilizátoru pro syntetické polymery a způsob stabilizace syntetického polymeru
DE4221068A1 (de)	1993-01-14	Bisbenzofuran-2-one
CZ196293A3 (en)	1994-04-13	Stabilizers based on 3-(dihydrobenyofuran-5-yl)benzofuran-2-ones
SK321090A3 (en)	1999-01-11	2,4-dimethyl-6-sec.alkyl-phenols, and stabilised organic materials them containing
US4617336A (en)	1986-10-14	Acylated calixarene stabilizers
EP0029803B1 (en)	1985-06-19	Organic polymeric materials stabilized with calcium stearoyl lactate
EP0081457B1 (de)	1987-10-07	Phenole und ihre Verwendung als Stabilisatoren
EP0145658B1 (de)	1987-07-08	Amide von Hydroxyphenylalkylthio-alkancarbonsäuren
EP0579576B1 (de)	1998-05-20	2,4-Dialkyl-6-sec-alkylphenole
US4560799A (en)	1985-12-24	Tri- and Tetra-(substituted hydroxyphenylthio) alkane and cycloalkane stabilizers and stabilized compositions
EP0249577B1 (de)	1991-12-04	Langketten-(4-Hydroxyphenyl)propionat-Derivate als Stabilisatoren
EP0252003B1 (de)	1991-08-21	Substituierte Aminoxysuccinate und deren Verwendung als Stabilisatoren
CA1292228C (en)	1991-11-19	Isocyanuric acid derivatives
US4612341A (en)	1986-09-16	Tri- and tetra-(substituted hydroxyphenylthio) alkane and cycloalkane stabilizers
EP0152022B1 (de)	1988-10-05	Di-(substituiertes hydroxyphenylthio)-alkane und -cycloalkane und sie enthaltende Stoffzusammensetzungen
US4810740A (en)	1989-03-07	Stabilized organic material
KR100229150B1 (ko)	1999-11-01	디페닐 아세트산 유도체 및 이들을 함유하는 조성물