NO310421B1 - Blandinger av blokkoligomerer inneholdende 2,2,6,6-tetrametyl- 4-piperidyl-grupper som stabilisatorer for organiske materialer - Google Patents

Info

Publication number

NO310421B1

NO310421B1 NO19965150A NO965150A NO310421B1 NO 310421 B1 NO310421 B1 NO 310421B1 NO 19965150 A NO19965150 A NO 19965150A NO 965150 A NO965150 A NO 965150A NO 310421 B1 NO310421 B1 NO 310421B1

Authority

NO

Norway

Prior art keywords

formula

alkyl

substituted

unsubstituted

group

Prior art date

1995-12-04

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• 239000000203 mixture Substances 0.000 title claims description 190
• -1 2,2,6,6-tetramethyl-4-piperidyl groups Chemical group 0.000 title claims description 144
• 239000011368 organic material Substances 0.000 title claims description 18
• 239000003381 stabilizer Substances 0.000 title description 17
• 150000001875 compounds Chemical class 0.000 claims description 156
• 229910052739 hydrogen Inorganic materials 0.000 claims description 46
• 239000001257 hydrogen Substances 0.000 claims description 45
• 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 38
• 125000000217 alkyl group Chemical group 0.000 claims description 33
• 239000004743 Polypropylene Substances 0.000 claims description 30
• 150000002431 hydrogen Chemical class 0.000 claims description 30
• 229920001155 polypropylene Polymers 0.000 claims description 26
• 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 24
• 238000006243 chemical reaction Methods 0.000 claims description 23
• 238000000034 method Methods 0.000 claims description 19
• UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 15
• 125000003884 phenylalkyl group Chemical group 0.000 claims description 15
• 125000004573 morpholin-4-yl group Chemical group N1(CCOCC1)* 0.000 claims description 14
• 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 14
• 125000002947 alkylene group Chemical group 0.000 claims description 13
• 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 12
• 239000004698 Polyethylene Substances 0.000 claims description 11
• 229920000573 polyethylene Polymers 0.000 claims description 11
• 125000000753 cycloalkyl group Chemical group 0.000 claims description 9
• 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 claims description 8
• 125000004200 2-methoxyethyl group Chemical group [H]C([H])([H])OC([H])([H])C([H])([H])* 0.000 claims description 8
• 125000003342 alkenyl group Chemical group 0.000 claims description 8
• 150000007529 inorganic bases Chemical class 0.000 claims description 8
• 230000003647 oxidation Effects 0.000 claims description 8
• 238000007254 oxidation reaction Methods 0.000 claims description 8
• 230000015556 catabolic process Effects 0.000 claims description 7
• 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 7
• 238000006731 degradation reaction Methods 0.000 claims description 7
• FDAKZQLBIFPGSV-UHFFFAOYSA-N n-butyl-2,2,6,6-tetramethylpiperidin-4-amine Chemical group CCCCNC1CC(C)(C)NC(C)(C)C1 FDAKZQLBIFPGSV-UHFFFAOYSA-N 0.000 claims description 7
• 239000003960 organic solvent Substances 0.000 claims description 7
• 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 claims description 5
• 238000004519 manufacturing process Methods 0.000 claims description 5
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• 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims description 4
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• 230000000087 stabilizing effect Effects 0.000 claims description 4
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