SK285104B6 - Synergická stabilizátorová zmes, kompozícia s jej obsahom a spôsob stabilizácie organického materiálu - Google Patents

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Publication number

SK285104B6

SK285104B6 SK461-96A SK46196A SK285104B6 SK 285104 B6 SK285104 B6 SK 285104B6 SK 46196 A SK46196 A SK 46196A SK 285104 B6 SK285104 B6 SK 285104B6

Authority

SK

Slovakia

Prior art keywords

carbon atoms

group

formula

compound

component

Prior art date

1995-04-11

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• 239000000203 mixture Substances 0.000 title claims abstract description 103
• 239000003381 stabilizer Substances 0.000 title claims abstract description 69
• 239000011368 organic material Substances 0.000 title claims description 18
• 238000000034 method Methods 0.000 title claims description 12
• 230000002195 synergetic effect Effects 0.000 title abstract description 6
• 230000006641 stabilisation Effects 0.000 title 1
• 238000011105 stabilization Methods 0.000 title 1
• 125000004432 carbon atom Chemical group C* 0.000 claims description 313
• 125000000217 alkyl group Chemical group 0.000 claims description 150
• -1 2,2,6,6-tetramethylpiperidin-4-yl groups Chemical group 0.000 claims description 108
• 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 79
• 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 76
• 125000000753 cycloalkyl group Chemical group 0.000 claims description 72
• 125000002947 alkylene group Chemical group 0.000 claims description 68
• 238000006731 degradation reaction Methods 0.000 claims description 43
• 125000003884 phenylalkyl group Chemical group 0.000 claims description 42
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• 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 32
• 230000015556 catabolic process Effects 0.000 claims description 29
• 238000006243 chemical reaction Methods 0.000 claims description 27
• 229910052757 nitrogen Inorganic materials 0.000 claims description 26
• 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 20
• 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 16
• 125000004433 nitrogen atom Chemical group N* 0.000 claims description 16
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• YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 claims description 9
• 229910052799 carbon Inorganic materials 0.000 claims description 7
• 229910052739 hydrogen Inorganic materials 0.000 claims description 7
• 125000002347 octyl 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])[H] 0.000 claims description 7
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• 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 6
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