SK280307B6

SK280307B6 - 2,4-dialkyl-6-sek.alkylfenoly, kompozície obsahujú

2,4-dialkyl-6-sek.alkylfenoly, kompozície obsahujú Download PDF

Info

Publication number: SK280307B6
Authority: SK; Slovakia
Prior art keywords: tert; compounds; formula; butyl; styrene
Prior art date: 1992-07-15

Application number

SK735-93A

Other languages

English (en)

Slovak (sk)

Other versions

SK73593A3 (en

Inventor

Paul Dubs

Rita Pitteloud

Original Assignee

Ciba Specialty Chemicals Holding Inc.

Priority date

1992-07-15

Filing date

1993-07-13

Publication date

1999-11-08

1993-07-13 Application filed by Ciba Specialty Chemicals Holding Inc. filed Critical Ciba Specialty Chemicals Holding Inc.

1994-06-08 Publication of SK73593A3 publication Critical patent/SK73593A3/sk

1999-11-08 Publication of SK280307B6 publication Critical patent/SK280307B6/sk

Links

150000001875 compounds Chemical class 0.000 title claims abstract description 69
239000000203 mixture Substances 0.000 title claims description 53
-1 alpha, alpha-dimethylbenzyl Chemical group 0.000 claims abstract description 88
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims abstract description 28
125000004432 carbon atom Chemical group C* 0.000 claims abstract description 22
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims abstract description 19
239000011368 organic material Substances 0.000 claims abstract description 17
125000000217 alkyl group Chemical group 0.000 claims abstract description 16
230000015556 catabolic process Effects 0.000 claims abstract description 9
238000006731 degradation reaction Methods 0.000 claims abstract description 9
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 37
229920001577 copolymer Polymers 0.000 claims description 35
239000004952 Polyamide Substances 0.000 claims description 13
229920000122 acrylonitrile butadiene styrene Polymers 0.000 claims description 13
229920002647 polyamide Polymers 0.000 claims description 13
XECAHXYUAAWDEL-UHFFFAOYSA-N acrylonitrile butadiene styrene Chemical compound C=CC=C.C=CC#N.C=CC1=CC=CC=C1 XECAHXYUAAWDEL-UHFFFAOYSA-N 0.000 claims description 11
239000004676 acrylonitrile butadiene styrene Substances 0.000 claims description 11
229920006324 polyoxymethylene Polymers 0.000 claims description 10
239000004721 Polyphenylene oxide Substances 0.000 claims description 9
239000004793 Polystyrene Substances 0.000 claims description 9
239000004417 polycarbonate Substances 0.000 claims description 9
229920002223 polystyrene Polymers 0.000 claims description 9
230000001590 oxidative effect Effects 0.000 claims description 7
229920000728 polyester Polymers 0.000 claims description 7
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239000004814 polyurethane Substances 0.000 claims description 7
125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 6
229920000515 polycarbonate Polymers 0.000 claims description 5
229920000098 polyolefin Polymers 0.000 claims description 5
229920002635 polyurethane Polymers 0.000 claims description 5
229920001897 terpolymer Polymers 0.000 claims description 5
230000000087 stabilizing effect Effects 0.000 claims description 4
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150000003440 styrenes Chemical class 0.000 claims 2
XMCMLCLWNUDTFL-UHFFFAOYSA-N C=CCCC.C=CC1=CC=CC=C1 Chemical compound C=CCCC.C=CC1=CC=CC=C1 XMCMLCLWNUDTFL-UHFFFAOYSA-N 0.000 claims 1
239000010775 animal oil Substances 0.000 claims 1
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238000007254 oxidation reaction Methods 0.000 abstract description 8
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239000004816 latex Substances 0.000 description 4
HQKMJHAJHXVSDF-UHFFFAOYSA-L magnesium stearate Chemical compound [Mg+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O HQKMJHAJHXVSDF-UHFFFAOYSA-L 0.000 description 4
239000000178 monomer Substances 0.000 description 4
DNIAPMSPPWPWGF-UHFFFAOYSA-N monopropylene glycol Natural products CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 4
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150000002815 nickel Chemical class 0.000 description 4
WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 4
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125000001424 substituent group Chemical group 0.000 description 4
YODZTKMDCQEPHD-UHFFFAOYSA-N thiodiglycol Chemical compound OCCSCCO YODZTKMDCQEPHD-UHFFFAOYSA-N 0.000 description 4
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FJKROLUGYXJWQN-UHFFFAOYSA-N 4-hydroxybenzoic acid Chemical compound OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 3
LALMYSXJJWCRDR-UHFFFAOYSA-N 4-tert-butyl-2-hexadecan-2-yl-6-methylphenol Chemical compound CCCCCCCCCCCCCCC(C)C1=CC(C(C)(C)C)=CC(C)=C1O LALMYSXJJWCRDR-UHFFFAOYSA-N 0.000 description 3
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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
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230000032683 aging Effects 0.000 description 3
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CJZGTCYPCWQAJB-UHFFFAOYSA-L calcium stearate Chemical compound [Ca+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CJZGTCYPCWQAJB-UHFFFAOYSA-L 0.000 description 3
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150000001991 dicarboxylic acids Chemical class 0.000 description 3
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239000003446 ligand Substances 0.000 description 3
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TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 3
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OPSWAWSNPREEFQ-UHFFFAOYSA-K triphenoxyalumane Chemical class [Al+3].[O-]C1=CC=CC=C1.[O-]C1=CC=CC=C1.[O-]C1=CC=CC=C1 OPSWAWSNPREEFQ-UHFFFAOYSA-K 0.000 description 3
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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
GQEZCXVZFLOKMC-UHFFFAOYSA-N 1-hexadecene Chemical compound CCCCCCCCCCCCCCC=C GQEZCXVZFLOKMC-UHFFFAOYSA-N 0.000 description 2
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