JP2012532239A5 - - Google Patents

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Publication number

JP2012532239A5

JP2012532239A5 JP2012518890A JP2012518890A JP2012532239A5 JP 2012532239 A5 JP2012532239 A5 JP 2012532239A5 JP 2012518890 A JP2012518890 A JP 2012518890A JP 2012518890 A JP2012518890 A JP 2012518890A JP 2012532239 A5 JP2012532239 A5 JP 2012532239A5

Authority

JP

Japan

Prior art keywords

tetraalkylpiperidine

hydroxy

alkyl

bis

group

Prior art date

2010-06-29

Legal status (The legal status 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 status listed.)

Granted

Links

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• 125000001424 substituent group Chemical group 0.000 claims 24
• 229910052739 hydrogen Inorganic materials 0.000 claims 15
• 239000001257 hydrogen Substances 0.000 claims 15
• 239000000203 mixture Substances 0.000 claims 13
• UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 11
• QLZHNIAADXEJJP-UHFFFAOYSA-L dioxido-oxo-phenyl-$l^{5}-phosphane Chemical compound [O-]P([O-])(=O)C1=CC=CC=C1 QLZHNIAADXEJJP-UHFFFAOYSA-L 0.000 claims 7
• 125000000217 alkyl group Chemical group 0.000 claims 6
• OEGSFELAUARXKF-UHFFFAOYSA-N guanidine;phenylphosphonic acid Chemical class NC(N)=N.OP(O)(=O)C1=CC=CC=C1 OEGSFELAUARXKF-UHFFFAOYSA-N 0.000 claims 6
• 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 6
• WKRUQZJUAPORKC-UHFFFAOYSA-N 2-[[4,6-bis[4-(1-cyclohexyloxy-2,2,6,6-tetramethylpiperidin-4-yl)butylamino]-1,3,5-triazin-2-yl]amino]ethanol Chemical compound C1C(C)(C)N(OC2CCCCC2)C(C)(C)CC1CCCCNC(N=1)=NC(NCCO)=NC=1NCCCCC(CC1(C)C)CC(C)(C)N1OC1CCCCC1 WKRUQZJUAPORKC-UHFFFAOYSA-N 0.000 claims 4
• AYJOUNOHHNLBJP-UHFFFAOYSA-N 6-chloro-2-n,4-n-bis[4-(1-cyclohexyloxy-2,2,6,6-tetramethylpiperidin-4-yl)butyl]-1,3,5-triazine-2,4-diamine Chemical compound C1C(C)(C)N(OC2CCCCC2)C(C)(C)CC1CCCCNC(N=1)=NC(Cl)=NC=1NCCCCC(CC1(C)C)CC(C)(C)N1OC1CCCCC1 AYJOUNOHHNLBJP-UHFFFAOYSA-N 0.000 claims 4
• 150000001875 compounds Chemical class 0.000 claims 4
• 150000002431 hydrogen Chemical class 0.000 claims 4
• 229920000307 polymer substrate Polymers 0.000 claims 4
• 125000002252 acyl group Chemical group 0.000 claims 3
• 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 3
• FUSRYQFNOAIOLF-UHFFFAOYSA-N phenylphosphonic acid;1,3,5-triazine-2,4,6-triamine Chemical compound NC1=NC(N)=NC(N)=N1.OP(O)(=O)C1=CC=CC=C1 FUSRYQFNOAIOLF-UHFFFAOYSA-N 0.000 claims 3
• FYQOHJWNKFULEZ-UHFFFAOYSA-N 1-(2-hydroxy-2-methylpropoxy)-2,2,6,6-tetramethylpiperidin-4-ol Chemical compound CC(C)(O)CON1C(C)(C)CC(O)CC1(C)C FYQOHJWNKFULEZ-UHFFFAOYSA-N 0.000 claims 2
• FUVBNYKKKZSBCG-UHFFFAOYSA-N 1-(2-hydroxy-2-methylpropoxy)-2,2,6,6-tetramethylpiperidin-4-one Chemical compound CC(C)(O)CON1C(C)(C)CC(=O)CC1(C)C FUVBNYKKKZSBCG-UHFFFAOYSA-N 0.000 claims 2
• WICJDHJYOIJBDM-UHFFFAOYSA-N 1-[4-[butyl-[4-[butyl-[1-(2-hydroxy-2-methylpropoxy)-2,2,6,6-tetramethylpiperidin-4-yl]amino]-6-(2-hydroxyethylamino)-1,3,5-triazin-2-yl]amino]-2,2,6,6-tetramethylpiperidin-1-yl]oxy-2-methylpropan-2-ol Chemical compound N=1C(NCCO)=NC(N(CCCC)C2CC(C)(C)N(OCC(C)(C)O)C(C)(C)C2)=NC=1N(CCCC)C1CC(C)(C)N(OCC(C)(C)O)C(C)(C)C1 WICJDHJYOIJBDM-UHFFFAOYSA-N 0.000 claims 2
• OKELZJLBUAZSCL-UHFFFAOYSA-N 1-cyclohexyloxy-2,2,6,6-tetramethyl-n-octadecylpiperidin-4-amine Chemical compound CC1(C)CC(NCCCCCCCCCCCCCCCCCC)CC(C)(C)N1OC1CCCCC1 OKELZJLBUAZSCL-UHFFFAOYSA-N 0.000 claims 2
• -1 1-cyclohexyloxy-2,2,6,6-tetramethylpiperidin-4-yl Chemical group 0.000 claims 2
• KTNPVRSKFWZJEZ-UHFFFAOYSA-N 2,2,6,6-tetramethylpiperidin-1-amine Chemical compound CC1(C)CCCC(C)(C)N1N KTNPVRSKFWZJEZ-UHFFFAOYSA-N 0.000 claims 2
• VVISQEKWYPFFLK-UHFFFAOYSA-N 2-n,2-n,4-n,4-n-tetrabutyl-6-chloro-1,3,5-triazine-2,4-diamine Chemical compound CCCCN(CCCC)C1=NC(Cl)=NC(N(CCCC)CCCC)=N1 VVISQEKWYPFFLK-UHFFFAOYSA-N 0.000 claims 2
• RXFCIXRFAJRBSG-UHFFFAOYSA-N 3,2,3-tetramine Chemical compound NCCCNCCNCCCN RXFCIXRFAJRBSG-UHFFFAOYSA-N 0.000 claims 2
• 125000004648 C2-C8 alkenyl group Chemical group 0.000 claims 2
• KGUHWHHMNQPSRV-UHFFFAOYSA-N [1-(2-hydroxy-2-methylpropoxy)-2,2,6,6-tetramethylpiperidin-4-yl] octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OC1CC(C)(C)N(OCC(C)(C)O)C(C)(C)C1 KGUHWHHMNQPSRV-UHFFFAOYSA-N 0.000 claims 2
• JLOAPAGFWFMZLD-UHFFFAOYSA-N bis(1-cyclohexyloxy-2,2,6,6-tetramethylpiperidin-4-yl) hexanedioate Chemical compound CC1(C)CC(OC(=O)CCCCC(=O)OC2CC(C)(C)N(OC3CCCCC3)C(C)(C)C2)CC(C)(C)N1OC1CCCCC1 JLOAPAGFWFMZLD-UHFFFAOYSA-N 0.000 claims 2
• OSIVCXJNIBEGCL-UHFFFAOYSA-N bis(2,2,6,6-tetramethyl-1-octoxypiperidin-4-yl) decanedioate Chemical compound C1C(C)(C)N(OCCCCCCCC)C(C)(C)CC1OC(=O)CCCCCCCCC(=O)OC1CC(C)(C)N(OCCCCCCCC)C(C)(C)C1 OSIVCXJNIBEGCL-UHFFFAOYSA-N 0.000 claims 2
• DVXRGUXKOSSOHV-UHFFFAOYSA-N bis[1-(2-hydroxy-2-methylpropoxy)-2,2,6,6-tetramethylpiperidin-4-yl] decanedioate Chemical compound C1C(C)(C)N(OCC(C)(O)C)C(C)(C)CC1OC(=O)CCCCCCCCC(=O)OC1CC(C)(C)N(OCC(C)(C)O)C(C)(C)C1 DVXRGUXKOSSOHV-UHFFFAOYSA-N 0.000 claims 2
• WUXGYZUOHKJTEY-UHFFFAOYSA-N bis[1-(2-hydroxy-2-methylpropoxy)-2,2,6,6-tetramethylpiperidin-4-yl] hexanedioate Chemical compound C1C(C)(C)N(OCC(C)(O)C)C(C)(C)CC1OC(=O)CCCCC(=O)OC1CC(C)(C)N(OCC(C)(C)O)C(C)(C)C1 WUXGYZUOHKJTEY-UHFFFAOYSA-N 0.000 claims 2
• 125000006309 butyl amino group Chemical group 0.000 claims 2
• 150000001732 carboxylic acid derivatives Chemical class 0.000 claims 2
• 239000007795 chemical reaction product Substances 0.000 claims 2
• 125000004464 hydroxyphenyl group Chemical group 0.000 claims 2
• 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 2
• 239000000758 substrate Substances 0.000 claims 2
• 229920001169 thermoplastic Polymers 0.000 claims 2
• RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 claims 1
• 125000003358 C2-C20 alkenyl group Chemical group 0.000 claims 1
• 150000001336 alkenes Chemical class 0.000 claims 1
• 150000001735 carboxylic acids Chemical class 0.000 claims 1
• 229920001577 copolymer Polymers 0.000 claims 1
• 125000000753 cycloalkyl group Chemical group 0.000 claims 1
• 239000003063 flame retardant Substances 0.000 claims 1
• 229920001519 homopolymer Polymers 0.000 claims 1
• 238000000034 method Methods 0.000 claims 1
• 239000000178 monomer Substances 0.000 claims 1
• 229920000098 polyolefin Polymers 0.000 claims 1
• 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims 1
• 229920002554 vinyl polymer Polymers 0.000 claims 1
• 0 CCCCN(CCC)c1nc(C(C)(C)N(C)C(CC2(C)C)CC(C)(CCC(C)(CC(CC3(C)C)N(C)c4nc(N(*)C(CC5(C)C)CC(C)(C)N5OCCC)nc(C(CC)N(C)C(CC5(C)C)CC(C)(C)N5OCCC)n4)N3OCCC)N2OCCC)nc(N(CCCC)CCCC)n1 Chemical compound CCCCN(CCC)c1nc(C(C)(C)N(C)C(CC2(C)C)CC(C)(CCC(C)(CC(CC3(C)C)N(C)c4nc(N(*)C(CC5(C)C)CC(C)(C)N5OCCC)nc(C(CC)N(C)C(CC5(C)C)CC(C)(C)N5OCCC)n4)N3OCCC)N2OCCC)nc(N(CCCC)CCCC)n1 0.000 description 1
• FOAZNYCOPRTDAW-UHFFFAOYSA-N CCCCN(CCCC)c1nc(N(C)C(CC2(C)C)CC(C)(C)N2OCCC)nc(N(CCCC)CCCC)n1 Chemical compound CCCCN(CCCC)c1nc(N(C)C(CC2(C)C)CC(C)(C)N2OCCC)nc(N(CCCC)CCCC)n1 FOAZNYCOPRTDAW-UHFFFAOYSA-N 0.000 description 1