JP2014501642A5 - - Google Patents
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- Publication number
- JP2014501642A5 JP2014501642A5 JP2013544633A JP2013544633A JP2014501642A5 JP 2014501642 A5 JP2014501642 A5 JP 2014501642A5 JP 2013544633 A JP2013544633 A JP 2013544633A JP 2013544633 A JP2013544633 A JP 2013544633A JP 2014501642 A5 JP2014501642 A5 JP 2014501642A5
- Authority
- JP
- Japan
- Prior art keywords
- bis
- tetramethyl
- triazine
- hydroxy
- tetramethylpiperidin
- Prior art date
- 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
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- -1 —COOR 4 Chemical group 0.000 claims 58
- 238000000034 method Methods 0.000 claims 33
- 239000000203 mixture Substances 0.000 claims 30
- 229920000642 polymer Polymers 0.000 claims 21
- 125000000217 alkyl group Chemical group 0.000 claims 20
- 229910052739 hydrogen Inorganic materials 0.000 claims 19
- 125000001183 hydrocarbyl group Chemical group 0.000 claims 16
- 150000001875 compounds Chemical class 0.000 claims 15
- 239000001257 hydrogen Substances 0.000 claims 13
- 125000000753 cycloalkyl group Chemical group 0.000 claims 11
- 229910052757 nitrogen Inorganic materials 0.000 claims 10
- 239000003381 stabilizer Substances 0.000 claims 9
- RLHGFJMGWQXPBW-UHFFFAOYSA-N 2-hydroxy-3-(1h-imidazol-5-ylmethyl)benzamide Chemical compound NC(=O)C1=CC=CC(CC=2NC=NC=2)=C1O RLHGFJMGWQXPBW-UHFFFAOYSA-N 0.000 claims 8
- 229910052799 carbon Inorganic materials 0.000 claims 8
- 239000004611 light stabiliser Substances 0.000 claims 8
- 125000003118 aryl group Chemical group 0.000 claims 7
- 125000006659 (C1-C20) hydrocarbyl group Chemical group 0.000 claims 6
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 6
- 125000003545 alkoxy group Chemical group 0.000 claims 6
- 125000002877 alkyl aryl group Chemical group 0.000 claims 6
- 150000001412 amines Chemical class 0.000 claims 6
- 125000003710 aryl alkyl group Chemical group 0.000 claims 6
- VZWXIQHBIQLMPN-UHFFFAOYSA-N chromane Chemical compound C1=CC=C2CCCOC2=C1 VZWXIQHBIQLMPN-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
- OJMIONKXNSYLSR-UHFFFAOYSA-N phosphorous acid Chemical compound OP(O)O OJMIONKXNSYLSR-UHFFFAOYSA-N 0.000 claims 6
- 150000003254 radicals Chemical class 0.000 claims 6
- 239000007983 Tris buffer Substances 0.000 claims 5
- 125000005119 alkyl cycloalkyl group Chemical group 0.000 claims 5
- 150000002431 hydrogen Chemical class 0.000 claims 5
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 5
- UKJARPDLRWBRAX-UHFFFAOYSA-N n,n'-bis(2,2,6,6-tetramethylpiperidin-4-yl)hexane-1,6-diamine Chemical compound C1C(C)(C)NC(C)(C)CC1NCCCCCCNC1CC(C)(C)NC(C)(C)C1 UKJARPDLRWBRAX-UHFFFAOYSA-N 0.000 claims 5
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims 4
- 125000002252 acyl group Chemical group 0.000 claims 4
- 229920001577 copolymer Polymers 0.000 claims 4
- 125000001316 cycloalkyl alkyl group Chemical group 0.000 claims 4
- 150000002148 esters Chemical class 0.000 claims 4
- 229910052736 halogen Inorganic materials 0.000 claims 4
- 150000002367 halogens Chemical class 0.000 claims 4
- XRBCRPZXSCBRTK-UHFFFAOYSA-N phosphonous acid Chemical class OPO XRBCRPZXSCBRTK-UHFFFAOYSA-N 0.000 claims 4
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 4
- 229910052717 sulfur Inorganic materials 0.000 claims 4
- 239000011593 sulfur Substances 0.000 claims 4
- NZNAAUDJKMURFU-UHFFFAOYSA-N tetrakis(2,2,6,6-tetramethylpiperidin-4-yl) butane-1,2,3,4-tetracarboxylate Chemical compound C1C(C)(C)NC(C)(C)CC1OC(=O)CC(C(=O)OC1CC(C)(C)NC(C)(C)C1)C(C(=O)OC1CC(C)(C)NC(C)(C)C1)CC(=O)OC1CC(C)(C)NC(C)(C)C1 NZNAAUDJKMURFU-UHFFFAOYSA-N 0.000 claims 4
- NJPUGXZMKBZIQZ-UHFFFAOYSA-N 1,5-dioxaspiro[5.5]undecane-3,3-dicarboxylic acid Chemical compound O1CC(C(=O)O)(C(O)=O)COC11CCCCC1 NJPUGXZMKBZIQZ-UHFFFAOYSA-N 0.000 claims 3
- RKMGAJGJIURJSJ-UHFFFAOYSA-N 2,2,6,6-Tetramethylpiperidine Substances CC1(C)CCCC(C)(C)N1 RKMGAJGJIURJSJ-UHFFFAOYSA-N 0.000 claims 3
- BWJKLDGAAPQXGO-UHFFFAOYSA-N 2,2,6,6-tetramethyl-4-octadecoxypiperidine Chemical compound CCCCCCCCCCCCCCCCCCOC1CC(C)(C)NC(C)(C)C1 BWJKLDGAAPQXGO-UHFFFAOYSA-N 0.000 claims 3
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 claims 3
- RXFCIXRFAJRBSG-UHFFFAOYSA-N 3,2,3-tetramine Chemical compound NCCCNCCNCCCN RXFCIXRFAJRBSG-UHFFFAOYSA-N 0.000 claims 3
- SAEZGDDJKSBNPT-UHFFFAOYSA-N 3-dodecyl-1-(1,2,2,6,6-pentamethylpiperidin-4-yl)pyrrolidine-2,5-dione Chemical compound O=C1C(CCCCCCCCCCCC)CC(=O)N1C1CC(C)(C)N(C)C(C)(C)C1 SAEZGDDJKSBNPT-UHFFFAOYSA-N 0.000 claims 3
- SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 claims 3
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims 3
- 239000007795 chemical reaction product Substances 0.000 claims 3
- GVJHHUAWPYXKBD-UHFFFAOYSA-N d-alpha-tocopherol Natural products OC1=C(C)C(C)=C2OC(CCCC(C)CCCC(C)CCCC(C)C)(C)CCC2=C1C GVJHHUAWPYXKBD-UHFFFAOYSA-N 0.000 claims 3
- 229910052760 oxygen Inorganic materials 0.000 claims 3
- 239000001301 oxygen Substances 0.000 claims 3
- 125000003884 phenylalkyl group Chemical group 0.000 claims 3
- 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 claims 3
- 125000001424 substituent group Chemical group 0.000 claims 3
- VXTRPEFUPWORNH-UHFFFAOYSA-N 1-(1-acetyl-2,2,6,6-tetramethylpiperidin-4-yl)-3-dodecylpyrrolidine-2,5-dione Chemical compound O=C1C(CCCCCCCCCCCC)CC(=O)N1C1CC(C)(C)N(C(C)=O)C(C)(C)C1 VXTRPEFUPWORNH-UHFFFAOYSA-N 0.000 claims 2
- GXURZKWLMYOCDX-UHFFFAOYSA-N 2,2-bis(hydroxymethyl)propane-1,3-diol;dihydroxyphosphanyl dihydrogen phosphite Chemical compound OP(O)OP(O)O.OCC(CO)(CO)CO GXURZKWLMYOCDX-UHFFFAOYSA-N 0.000 claims 2
- IXAKLSFFPBJWBS-UHFFFAOYSA-N 2-cycloundecyl-7,7,9,9-tetramethyl-1-oxa-3,8-diazaspiro[4.5]decan-4-one Chemical compound C1C(C)(C)NC(C)(C)CC21C(=O)NC(C1CCCCCCCCCC1)O2 IXAKLSFFPBJWBS-UHFFFAOYSA-N 0.000 claims 2
- NPYDPROENPLGBR-UHFFFAOYSA-N 4,6-dichloro-n-cyclohexyl-1,3,5-triazin-2-amine Chemical compound ClC1=NC(Cl)=NC(NC2CCCCC2)=N1 NPYDPROENPLGBR-UHFFFAOYSA-N 0.000 claims 2
- STEYNUVPFMIUOY-UHFFFAOYSA-N 4-Hydroxy-1-(2-hydroxyethyl)-2,2,6,6-tetramethylpiperidine Chemical compound CC1(C)CC(O)CC(C)(C)N1CCO STEYNUVPFMIUOY-UHFFFAOYSA-N 0.000 claims 2
- ZCQXJDSFSOETQO-UHFFFAOYSA-N 8-acetyl-3-dodecyl-7,7,9,9-tetramethyl-1,3,8-triazaspiro[4.5]decane-2,4-dione;3-dodecyl-1-(2,2,6,6-tetramethylpiperidin-4-yl)pyrrolidine-2,5-dione Chemical compound O=C1C(CCCCCCCCCCCC)CC(=O)N1C1CC(C)(C)NC(C)(C)C1.O=C1N(CCCCCCCCCCCC)C(=O)NC11CC(C)(C)N(C(C)=O)C(C)(C)C1 ZCQXJDSFSOETQO-UHFFFAOYSA-N 0.000 claims 2
- OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 claims 2
- AVXURJPOCDRRFD-UHFFFAOYSA-N Hydroxylamine Chemical compound ON AVXURJPOCDRRFD-UHFFFAOYSA-N 0.000 claims 2
- LKJPYSCBVHEWIU-UHFFFAOYSA-N N-[4-cyano-3-(trifluoromethyl)phenyl]-3-[(4-fluorophenyl)sulfonyl]-2-hydroxy-2-methylpropanamide Chemical compound C=1C=C(C#N)C(C(F)(F)F)=CC=1NC(=O)C(O)(C)CS(=O)(=O)C1=CC=C(F)C=C1 LKJPYSCBVHEWIU-UHFFFAOYSA-N 0.000 claims 2
- JKIJEFPNVSHHEI-UHFFFAOYSA-N Phenol, 2,4-bis(1,1-dimethylethyl)-, phosphite (3:1) Chemical compound CC(C)(C)C1=CC(C(C)(C)C)=CC=C1OP(OC=1C(=CC(=CC=1)C(C)(C)C)C(C)(C)C)OC1=CC=C(C(C)(C)C)C=C1C(C)(C)C JKIJEFPNVSHHEI-UHFFFAOYSA-N 0.000 claims 2
- 239000006096 absorbing agent Substances 0.000 claims 2
- 239000000654 additive Substances 0.000 claims 2
- 125000002947 alkylene group Chemical group 0.000 claims 2
- NLMFVJSIGDIJBB-UHFFFAOYSA-N bis(2,2,6,6-tetramethyl-1-octoxypiperidin-3-yl) decanedioate Chemical compound CC1(C)N(OCCCCCCCC)C(C)(C)CCC1OC(=O)CCCCCCCCC(=O)OC1C(C)(C)N(OCCCCCCCC)C(C)(C)CC1 NLMFVJSIGDIJBB-UHFFFAOYSA-N 0.000 claims 2
- MGNCLNQXLYJVJD-UHFFFAOYSA-N cyanuric chloride Chemical compound ClC1=NC(Cl)=NC(Cl)=N1 MGNCLNQXLYJVJD-UHFFFAOYSA-N 0.000 claims 2
- LPIQUOYDBNQMRZ-UHFFFAOYSA-N cyclopentene Chemical compound C1CC=CC1 LPIQUOYDBNQMRZ-UHFFFAOYSA-N 0.000 claims 2
- DIOQZVSQGTUSAI-UHFFFAOYSA-N decane Chemical compound CCCCCCCCCC DIOQZVSQGTUSAI-UHFFFAOYSA-N 0.000 claims 2
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 claims 2
- KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical class [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 claims 2
- 125000003438 dodecyl 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])C([H])([H])C([H])([H])* 0.000 claims 2
- 239000012634 fragment Substances 0.000 claims 2
- FNAZRRHPUDJQCJ-UHFFFAOYSA-N henicosane Chemical compound CCCCCCCCCCCCCCCCCCCCC FNAZRRHPUDJQCJ-UHFFFAOYSA-N 0.000 claims 2
- 229920001903 high density polyethylene Polymers 0.000 claims 2
- 239000004700 high-density polyethylene Substances 0.000 claims 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 2
- 229920001684 low density polyethylene Polymers 0.000 claims 2
- 239000004702 low-density polyethylene Substances 0.000 claims 2
- 229920001179 medium density polyethylene Polymers 0.000 claims 2
- 239000004701 medium-density polyethylene Substances 0.000 claims 2
- GXELTROTKVKZBQ-UHFFFAOYSA-N n,n-dibenzylhydroxylamine Chemical compound C=1C=CC=CC=1CN(O)CC1=CC=CC=C1 GXELTROTKVKZBQ-UHFFFAOYSA-N 0.000 claims 2
- DHXOCDLHWYUUAG-UHFFFAOYSA-N n,n-didodecylhydroxylamine Chemical compound CCCCCCCCCCCCN(O)CCCCCCCCCCCC DHXOCDLHWYUUAG-UHFFFAOYSA-N 0.000 claims 2
- DUWWHGPELOTTOE-UHFFFAOYSA-N n-(5-chloro-2,4-dimethoxyphenyl)-3-oxobutanamide Chemical compound COC1=CC(OC)=C(NC(=O)CC(C)=O)C=C1Cl DUWWHGPELOTTOE-UHFFFAOYSA-N 0.000 claims 2
- BLBLVDQTHWVGRA-UHFFFAOYSA-N n-butyl-3-[4-[4-(butylamino)-1,2,2,6,6-pentamethylpiperidin-3-yl]-6-chloro-1,3,5-triazin-2-yl]-1,2,2,6,6-pentamethylpiperidin-4-amine Chemical compound CCCCNC1CC(C)(C)N(C)C(C)(C)C1C1=NC(Cl)=NC(C2C(N(C)C(C)(C)CC2NCCCC)(C)C)=N1 BLBLVDQTHWVGRA-UHFFFAOYSA-N 0.000 claims 2
- 125000001624 naphthyl group Chemical group 0.000 claims 2
- MGFYIUFZLHCRTH-UHFFFAOYSA-N nitrilotriacetic acid Chemical compound OC(=O)CN(CC(O)=O)CC(O)=O MGFYIUFZLHCRTH-UHFFFAOYSA-N 0.000 claims 2
- ZPNJBTBYIHBSIG-UHFFFAOYSA-N phenyl-(2,2,6,6-tetramethylpiperidin-4-yl)methanone Chemical compound C1C(C)(C)NC(C)(C)CC1C(=O)C1=CC=CC=C1 ZPNJBTBYIHBSIG-UHFFFAOYSA-N 0.000 claims 2
- 235000019260 propionic acid Nutrition 0.000 claims 2
- KDYFGRWQOYBRFD-UHFFFAOYSA-L succinate(2-) Chemical compound [O-]C(=O)CCC([O-])=O KDYFGRWQOYBRFD-UHFFFAOYSA-L 0.000 claims 2
- KDYFGRWQOYBRFD-UHFFFAOYSA-N succinic acid Chemical compound OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 claims 2
- 239000003760 tallow Substances 0.000 claims 2
- HVLLSGMXQDNUAL-UHFFFAOYSA-N triphenyl phosphite Chemical group C=1C=CC=CC=1OP(OC=1C=CC=CC=1)OC1=CC=CC=C1 HVLLSGMXQDNUAL-UHFFFAOYSA-N 0.000 claims 2
- 229920000785 ultra high molecular weight polyethylene Polymers 0.000 claims 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 claims 1
- JMUOXOJMXILBTE-UHFFFAOYSA-N (2,2,6,6-tetramethylpiperidin-4-yl) octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OC1CC(C)(C)NC(C)(C)C1 JMUOXOJMXILBTE-UHFFFAOYSA-N 0.000 claims 1
- HJIAMFHSAAEUKR-UHFFFAOYSA-N (2-hydroxyphenyl)-phenylmethanone Chemical group OC1=CC=CC=C1C(=O)C1=CC=CC=C1 HJIAMFHSAAEUKR-UHFFFAOYSA-N 0.000 claims 1
- 125000006657 (C1-C10) hydrocarbyl group Chemical group 0.000 claims 1
- 125000004642 (C1-C12) alkoxy group Chemical group 0.000 claims 1
- FIDRAVVQGKNYQK-UHFFFAOYSA-N 1,2,3,4-tetrahydrotriazine Chemical compound C1NNNC=C1 FIDRAVVQGKNYQK-UHFFFAOYSA-N 0.000 claims 1
- JYEUMXHLPRZUAT-UHFFFAOYSA-N 1,2,3-triazine Chemical compound C1=CN=NN=C1 JYEUMXHLPRZUAT-UHFFFAOYSA-N 0.000 claims 1
- QDYOUVZODPKHBI-UHFFFAOYSA-N 1,3,5,7,9,11-hexazatetracyclo[9.2.1.05,13.07,12]tetradeca-2,8,12-triene-6,14-dione Chemical compound C1N=CN2C(=O)N3C4=C2N1C(=O)N4C=NC3 QDYOUVZODPKHBI-UHFFFAOYSA-N 0.000 claims 1
- VNQNXQYZMPJLQX-UHFFFAOYSA-N 1,3,5-tris[(3,5-ditert-butyl-4-hydroxyphenyl)methyl]-1,3,5-triazinane-2,4,6-trione Chemical compound CC(C)(C)C1=C(O)C(C(C)(C)C)=CC(CN2C(N(CC=3C=C(C(O)=C(C=3)C(C)(C)C)C(C)(C)C)C(=O)N(CC=3C=C(C(O)=C(C=3)C(C)(C)C)C(C)(C)C)C2=O)=O)=C1 VNQNXQYZMPJLQX-UHFFFAOYSA-N 0.000 claims 1
- XYXJKPCGSGVSBO-UHFFFAOYSA-N 1,3,5-tris[(4-tert-butyl-3-hydroxy-2,6-dimethylphenyl)methyl]-1,3,5-triazinane-2,4,6-trione Chemical compound CC1=CC(C(C)(C)C)=C(O)C(C)=C1CN1C(=O)N(CC=2C(=C(O)C(=CC=2C)C(C)(C)C)C)C(=O)N(CC=2C(=C(O)C(=CC=2C)C(C)(C)C)C)C1=O XYXJKPCGSGVSBO-UHFFFAOYSA-N 0.000 claims 1
- FFIJIFGRYNWQNQ-UHFFFAOYSA-N 1-(2,2,6,6-tetramethylpiperidin-4-yl)pyrrole-2,5-dione Chemical compound C1C(C)(C)NC(C)(C)CC1N1C(=O)C=CC1=O FFIJIFGRYNWQNQ-UHFFFAOYSA-N 0.000 claims 1
- 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 1
- GSOBQKOVISZSEE-UHFFFAOYSA-N 1-(triazin-4-yl)piperazin-2-one Chemical compound O=C1CNCCN1C1=CC=NN=N1 GSOBQKOVISZSEE-UHFFFAOYSA-N 0.000 claims 1
- QSSWKPVVDJURMQ-UHFFFAOYSA-N 2,2,4,4,6-pentamethyl-1,3-diazinane Chemical compound CC1CC(C)(C)NC(C)(C)N1 QSSWKPVVDJURMQ-UHFFFAOYSA-N 0.000 claims 1
- HWRLEEPNFJNTOP-UHFFFAOYSA-N 2-(1,3,5-triazin-2-yl)phenol Chemical class OC1=CC=CC=C1C1=NC=NC=N1 HWRLEEPNFJNTOP-UHFFFAOYSA-N 0.000 claims 1
- FJGQBLRYBUAASW-UHFFFAOYSA-N 2-(benzotriazol-2-yl)phenol Chemical class OC1=CC=CC=C1N1N=C2C=CC=CC2=N1 FJGQBLRYBUAASW-UHFFFAOYSA-N 0.000 claims 1
- WDSZRYWCOPYDJE-UHFFFAOYSA-N 2-[4,6-bis(2,4-dimethylphenyl)-1,3,5-triazin-2-yl]-5-(2-hydroxy-3-nonoxypropoxy)-4-(2-phenylpropan-2-yl)phenol Chemical compound CCCCCCCCCOCC(O)COC1=CC(O)=C(C=2N=C(N=C(N=2)C=2C(=CC(C)=CC=2)C)C=2C(=CC(C)=CC=2)C)C=C1C(C)(C)C1=CC=CC=C1 WDSZRYWCOPYDJE-UHFFFAOYSA-N 0.000 claims 1
- CTQAYJKMGXQVQH-UHFFFAOYSA-N 2-[4,6-bis(2,4-dimethylphenyl)-1,3,5-triazin-2-yl]-5-(2-hydroxy-3-phenylmethoxypropoxy)phenol Chemical compound CC1=CC(C)=CC=C1C1=NC(C=2C(=CC(C)=CC=2)C)=NC(C=2C(=CC(OCC(O)COCC=3C=CC=CC=3)=CC=2)O)=N1 CTQAYJKMGXQVQH-UHFFFAOYSA-N 0.000 claims 1
- WYLMGXULBMHUDT-UHFFFAOYSA-N 2-[4,6-bis(2,4-dimethylphenyl)-1,3,5-triazin-2-yl]-5-[3-(2-ethylhexoxy)-2-hydroxypropoxy]phenol Chemical compound OC1=CC(OCC(O)COCC(CC)CCCC)=CC=C1C1=NC(C=2C(=CC(C)=CC=2)C)=NC(C=2C(=CC(C)=CC=2)C)=N1 WYLMGXULBMHUDT-UHFFFAOYSA-N 0.000 claims 1
- WPMUMRCRKFBYIH-UHFFFAOYSA-N 2-[4,6-bis(2-hydroxy-4-octoxyphenyl)-1,3,5-triazin-2-yl]-5-octoxyphenol Chemical compound OC1=CC(OCCCCCCCC)=CC=C1C1=NC(C=2C(=CC(OCCCCCCCC)=CC=2)O)=NC(C=2C(=CC(OCCCCCCCC)=CC=2)O)=N1 WPMUMRCRKFBYIH-UHFFFAOYSA-N 0.000 claims 1
- ZBUFTVMOMCQOFV-UHFFFAOYSA-N 2-[4,6-bis(4-phenylphenyl)-1,3,5-triazin-2-yl]-5-(2-ethylhexoxy)phenol Chemical compound OC1=CC(OCC(CC)CCCC)=CC=C1C1=NC(C=2C=CC(=CC=2)C=2C=CC=CC=2)=NC(C=2C=CC(=CC=2)C=2C=CC=CC=2)=N1 ZBUFTVMOMCQOFV-UHFFFAOYSA-N 0.000 claims 1
- GZQKBPSHUCTQCZ-UHFFFAOYSA-N 2-[4,6-bis[4-(3-butan-2-yloxy-2-hydroxypropoxy)-2-hydroxyphenyl]-1,3,5-triazin-2-yl]-5-(3-butan-2-yloxy-2-hydroxypropoxy)phenol Chemical compound OC1=CC(OCC(O)COC(C)CC)=CC=C1C1=NC(C=2C(=CC(OCC(O)COC(C)CC)=CC=2)O)=NC(C=2C(=CC(OCC(O)COC(C)CC)=CC=2)O)=N1 GZQKBPSHUCTQCZ-UHFFFAOYSA-N 0.000 claims 1
- VVBVFVRWEMORTQ-UHFFFAOYSA-N 2-[4-(4,6-diphenyl-1,3,5-triazin-2-yl)-3-hydroxyphenoxy]ethyl 2-ethylhexanoate Chemical compound OC1=CC(OCCOC(=O)C(CC)CCCC)=CC=C1C1=NC(C=2C=CC=CC=2)=NC(C=2C=CC=CC=2)=N1 VVBVFVRWEMORTQ-UHFFFAOYSA-N 0.000 claims 1
- JPGKCKOKTLQEOD-UHFFFAOYSA-N 2-[4-(4-bromophenyl)-6-[2-hydroxy-4-(2-hydroxyethoxy)phenyl]-1,3,5-triazin-2-yl]-5-(2-hydroxyethoxy)phenol Chemical compound OC1=CC(OCCO)=CC=C1C1=NC(C=2C=CC(Br)=CC=2)=NC(C=2C(=CC(OCCO)=CC=2)O)=N1 JPGKCKOKTLQEOD-UHFFFAOYSA-N 0.000 claims 1
- CWVUGNSYIROMGD-UHFFFAOYSA-N 2-[4-(4-chlorophenyl)-6-[2-hydroxy-4-(2-hydroxyethoxy)phenyl]-1,3,5-triazin-2-yl]-5-(2-hydroxyethoxy)phenol Chemical compound OC1=CC(OCCO)=CC=C1C1=NC(C=2C=CC(Cl)=CC=2)=NC(C=2C(=CC(OCCO)=CC=2)O)=N1 CWVUGNSYIROMGD-UHFFFAOYSA-N 0.000 claims 1
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- RFOHWLRXZVHOBB-UHFFFAOYSA-N n-butyl-2,2,6,6-tetramethylpiperidin-1-amine Chemical compound CCCCNN1C(C)(C)CCCC1(C)C RFOHWLRXZVHOBB-UHFFFAOYSA-N 0.000 claims 1
- FDAKZQLBIFPGSV-UHFFFAOYSA-N n-butyl-2,2,6,6-tetramethylpiperidin-4-amine Chemical compound CCCCNC1CC(C)(C)NC(C)(C)C1 FDAKZQLBIFPGSV-UHFFFAOYSA-N 0.000 claims 1
- JQARHBQLKPQLRB-UHFFFAOYSA-N n-heptadecyl-n-hexadecylhydroxylamine Chemical compound CCCCCCCCCCCCCCCCCN(O)CCCCCCCCCCCCCCCC JQARHBQLKPQLRB-UHFFFAOYSA-N 0.000 claims 1
- ZRPOKHXBOZQSOX-UHFFFAOYSA-N n-heptadecyl-n-octadecylhydroxylamine Chemical compound CCCCCCCCCCCCCCCCCCN(O)CCCCCCCCCCCCCCCCC ZRPOKHXBOZQSOX-UHFFFAOYSA-N 0.000 claims 1
- WGCBLWIBXXQTAW-UHFFFAOYSA-N n-hexadecyl-n-octadecylhydroxylamine Chemical compound CCCCCCCCCCCCCCCCCCN(O)CCCCCCCCCCCCCCCC WGCBLWIBXXQTAW-UHFFFAOYSA-N 0.000 claims 1
- IUMKEVRMAYGUGZ-UHFFFAOYSA-N n-hexadecyl-n-tetradecylhydroxylamine Chemical compound CCCCCCCCCCCCCCCCN(O)CCCCCCCCCCCCCC IUMKEVRMAYGUGZ-UHFFFAOYSA-N 0.000 claims 1
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 claims 1
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- 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 claims 1
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Families Citing this family (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US11267951B2 (en) | 2010-12-13 | 2022-03-08 | Cytec Technology Corp. | Stabilizer compositions containing substituted chroman compounds and methods of use |
| US20130168128A1 (en) * | 2011-12-29 | 2013-07-04 | Viakable, S. A. De C. V. | Sun-light resistant self-lubricated insulated conductor |
| NZ726849A (en) * | 2012-06-13 | 2018-06-29 | Cytec Tech Corp | Stabilizer compositions containing substituted chroman compounds and methods of use |
| WO2014190298A1 (en) * | 2013-05-24 | 2014-11-27 | Dow Global Technologies Llc | An ethylene-based composition |
| KR101635519B1 (ko) * | 2013-11-29 | 2016-07-04 | 롯데케미칼 주식회사 | 가교화 회전 성형용 폴리에틸렌 수지 조성물 및 이로부터 형성된 수지 성형품 |
| TWI760297B (zh) | 2014-11-20 | 2022-04-11 | 美商塞特工業公司 | 安定劑組合物及使用該組合物以保護有機材料抵抗ｕｖ光及熱降解之方法 |
| US10570270B2 (en) | 2016-11-18 | 2020-02-25 | Equistar Chemicals, Lp | Polyolefin materials for rotational molding applications having improved impact properties and color stability |
| EP3578599A1 (en) | 2018-06-08 | 2019-12-11 | Cytec Industries Inc. | Granular stabilizer compositions for use in polymer resins and methods of making same |
| US11827767B2 (en) † | 2018-07-12 | 2023-11-28 | Lg Chem, Ltd. | Plasticizer composition comprising cyclohexane polyester-based substance and resin composition comprising the same |
| CN112771108B (zh) | 2018-08-22 | 2023-05-05 | 巴斯夫欧洲公司 | 稳定的滚塑聚烯烃 |
| WO2020217482A1 (ja) * | 2019-04-26 | 2020-10-29 | 株式会社ユポ・コーポレーション | 樹脂組成物及び樹脂シート |
| KR102270026B1 (ko) * | 2020-01-31 | 2021-06-28 | 현대약품 주식회사 | (3s)-3-(4-(3-(1,4-다이옥사스파이로[4,5]데스-7-엔-8-일)벤질옥시)페닐)헥스-4-이노익산의 품질 평가 방법 |
| WO2024083872A1 (en) | 2022-10-18 | 2024-04-25 | Cytec Industries Inc. | Synergistic stabilizer compositions and methods for using same for protecting organic materials from uv light and thermal degradation |
| WO2025056330A1 (en) | 2023-09-13 | 2025-03-20 | Cytec Industries Inc. | Stabilized polymer compositions with improved color resistance |
| PL448056A1 (pl) * | 2024-03-20 | 2025-09-22 | Politechnika Łódzka | Kompozycja elastomerowa przeznaczone na wyroby polimerowe o podwyższonej odporności na utlenianie |
| WO2025219501A1 (en) | 2024-04-17 | 2025-10-23 | Cytec Industries Inc. | Stabilizing compositions for polymeric materials |
Family Cites Families (88)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5455043A (en) | 1977-10-12 | 1979-05-01 | Mitsui Petrochem Ind Ltd | Polyolefin compound |
| GB2042562B (en) | 1979-02-05 | 1983-05-11 | Sandoz Ltd | Stabilising polymers |
| US4240961A (en) | 1979-05-29 | 1980-12-23 | The B. F. Goodrich Company | Synthesis of 2-piperazinones and 1,4-diaza-2-keto-cycloheptanes |
| JPS5896638A (ja) | 1981-12-04 | 1983-06-08 | Asahi Chem Ind Co Ltd | 重合体組成物 |
| US4480092A (en) | 1982-02-19 | 1984-10-30 | The B. F. Goodrich Company | Alkylated polyalkylenepolyamines, substituted oxo-piperazinyl-triazines |
| US4639479A (en) | 1982-02-19 | 1987-01-27 | The Bfgoodrich Company | Polyalkylenepolyamine having pendant substituted oxo-piperazinyltriazines and UV light stabilized compositions |
| US4489099A (en) | 1983-02-28 | 1984-12-18 | The Goodyear Tire & Rubber Company | Vitamin E/DLTDP stabilizer system for chewing gum SBR |
| EP0183869B1 (en) | 1984-12-06 | 1991-04-17 | Kuraray Co., Ltd. | Chroman compounds and their use |
| CA1241009A (en) | 1984-12-07 | 1988-08-23 | Manzo Shiono | Chroman compounds and uses thereof |
| US4629752A (en) | 1985-07-22 | 1986-12-16 | The B. F. Goodrich Company | Substituted oxo-piperazinyl-triazines and UV light stabilized compositions |
| DE3634531A1 (de) | 1986-10-10 | 1988-04-14 | Basf Ag | Stabilisatorgemische fuer kunststoffe |
| US4797438A (en) | 1987-05-11 | 1989-01-10 | The B. F. Goodrich Company | Stabilized gamma-irradiated polypropylene and sterilizable articles thereof |
| DE3735577A1 (de) | 1987-10-21 | 1989-05-03 | Basf Ag | Gemisch zum stabilisieren von polyurethanen |
| JPH01170632A (ja) | 1987-12-26 | 1989-07-05 | Sakai Chem Ind Co Ltd | 樹脂組成物 |
| US5262471A (en) * | 1988-11-21 | 1993-11-16 | Fuji Photo Film Co., Ltd. | Method of preparing packaging material for photographic photosensitive material and masterbatch therefor |
| DE58906177D1 (de) | 1988-12-23 | 1993-12-16 | Basf Ag | Stabilisatorgemische für kunststoffe. |
| EP0384472B1 (en) | 1989-02-23 | 1997-09-10 | Fuji Photo Film Co., Ltd. | Resin composition and packaging material for photosensitive materials |
| JPH0335552A (ja) | 1989-06-30 | 1991-02-15 | Nec Kansai Ltd | 高耐圧半導体装置 |
| JP2813891B2 (ja) * | 1989-07-07 | 1998-10-22 | 住友化学工業株式会社 | 食品容器 |
| US5175312A (en) | 1989-08-31 | 1992-12-29 | Ciba-Geigy Corporation | 3-phenylbenzofuran-2-ones |
| US5013836A (en) | 1989-11-21 | 1991-05-07 | The B. F. Goodrich Company | Process for methylating a hindered nitrogen atom in a polysubstituted diazacycloalkan-2-one |
| TW206220B (cg-RX-API-DMAC7.html) | 1991-07-01 | 1993-05-21 | Ciba Geigy Ag | |
| US5252643A (en) | 1991-07-01 | 1993-10-12 | Ciba-Geigy Corporation | Thiomethylated benzofuran-2-ones |
| GB9121575D0 (en) * | 1991-10-11 | 1991-11-27 | Sandoz Ltd | Improvements in or relating to organic compounds |
| US5308549A (en) | 1991-11-12 | 1994-05-03 | Hoffmann-La Roche Inc. | Stabilizers for thermo plastic materials |
| US5218008A (en) | 1991-11-13 | 1993-06-08 | The Dow Chemical Company | Polyethers stabilized with 6-chromanol derivatives |
| US5310771A (en) | 1992-04-23 | 1994-05-10 | Phillips Petroleum Company | Polyolefin stabilization |
| TW260686B (cg-RX-API-DMAC7.html) | 1992-05-22 | 1995-10-21 | Ciba Geigy | |
| GB2267490B (en) | 1992-05-22 | 1995-08-09 | Ciba Geigy Ag | 3-(Carboxymethoxyphenyl)benzofuran-2-one stabilisers |
| NL9300801A (nl) | 1992-05-22 | 1993-12-16 | Ciba Geigy | 3-(acyloxyfenyl)benzofuran-2-on als stabilisatoren. |
| MX9305489A (es) | 1992-09-23 | 1994-03-31 | Ciba Geigy Ag | 3-(dihidrobenzofuran-5-il)benzofuran-2-onas, estabilizadores. |
| TW255902B (cg-RX-API-DMAC7.html) | 1992-09-23 | 1995-09-01 | Ciba Geigy | |
| CH686306A5 (de) | 1993-09-17 | 1996-02-29 | Ciba Geigy Ag | 3-Aryl-benzofuranone als Stabilisatoren. |
| US5357020A (en) * | 1993-09-29 | 1994-10-18 | Union Carbide Chemicals & Plastics Technology Corporation | Polysiloxane with chromanol moiety |
| WO1995019391A1 (en) * | 1994-01-14 | 1995-07-20 | Exxon Chemical Patents Inc. | Gas fade resistant ultraviolet additive formulations for polyethylene |
| DE4405670A1 (de) | 1994-02-23 | 1995-08-24 | Basf Ag | Stabilisatorgemisch aus Chromanderivaten, organischen Phosphiten oder Phosphoniten und Aminen |
| TW297822B (cg-RX-API-DMAC7.html) * | 1994-04-13 | 1997-02-11 | Ciba Geigy Ag | |
| CA2146034A1 (en) | 1994-05-12 | 1995-11-13 | Kenneth W. Willcox | Polymer stabilization |
| DE4420769A1 (de) * | 1994-06-15 | 1995-12-21 | Basf Ag | Mit alpha-Tocopherol stabilisierte Styrol/Butadien-Blockcopolymere |
| DE19501053A1 (de) | 1995-01-16 | 1996-07-18 | Basf Ag | Stabilisatorgemisch aus Chromanderivaten und inerten organischen Lösungsmitteln sowie dieses Stabilisatorgemisch enthaltende Mikrokapseln |
| US5594055A (en) | 1995-02-22 | 1997-01-14 | Hoffmann-La Roche Inc. | Antioxidant system for polyolefins |
| USH1600H (en) * | 1995-03-27 | 1996-10-01 | Quantum Chemical Company | High density polyethylenes with improved processing stability |
| DE19516283A1 (de) | 1995-05-04 | 1996-11-07 | Basf Ag | Thermoplastische Formmasse |
| DE19524178A1 (de) | 1995-07-03 | 1997-01-09 | Basf Ag | Thermoplastische Formmassen sowie ein Verfahren zur Reduzierung der Bildung von Restmonomeren in diesen Formmassen |
| AU6613296A (en) | 1995-07-20 | 1997-02-18 | Basf Aktiengesellschaft | Chroman derivatives, their preparation and their use as stabilizers of organic material against light, oxygen and heat |
| TW438850B (en) | 1995-09-15 | 2001-06-07 | Ciba Sc Holding Ag | Stabilization of polyolefin composition in permanent contact with extracting media |
| US5844027A (en) | 1996-05-03 | 1998-12-01 | Ciba Specialty Chemicals Corporation | Stabilizer composition for thermoplastic materials |
| GB9613515D0 (en) | 1996-06-27 | 1996-08-28 | Clariant Int Ltd | Stabilizer compositions |
| EP0839623B1 (de) | 1996-10-30 | 2001-01-31 | Ciba SC Holding AG | Stabilisatorkombination für das Rotomolding-Verfahren |
| IT1289935B1 (it) | 1997-02-20 | 1998-10-19 | Great Lakes Chemical Italia | Forma solida di uno stabilizzante per polimeri organici |
| US5844026A (en) | 1997-06-30 | 1998-12-01 | Ciba Specialty Chemicals Corporation | N,N',N''-tris{2,4-bis Hydrocarbyloxy-2,2,6,6-tetra-methylpiperidin-4-yl)alkylamino!-s-triazin-6-yl}-3,3'-ethylenediiminodipropylamines, their isomers and bridged derivatives and polymer compositions stabilized therewith |
| US6468258B1 (en) | 1997-07-18 | 2002-10-22 | Baxter International Inc. | Plastic compositions including vitamin E for medical containers and methods for providing such compositions and containers |
| WO1999054394A1 (en) * | 1998-04-17 | 1999-10-28 | Yoshitomi Fine Chemicals, Ltd. | Stabilizer for organic polymeric material and organic polymeric material composition |
| US6465548B1 (en) | 1997-10-02 | 2002-10-15 | Yoshitomi Fine Chemicals, Ltd. | Stabilizer for organic polymer material and organic polymer material composition |
| WO1999048997A1 (en) * | 1998-03-24 | 1999-09-30 | Ciba Specialty Chemicals Holding Inc. | Stabilisation of organic materials |
| US6051164A (en) * | 1998-04-30 | 2000-04-18 | Cytec Technology Corp. | Methods and compositions for protecting polymers from UV light |
| GB2344103B (en) | 1998-11-24 | 2003-04-16 | Ciba Sc Holding Ag | Piperazinone derivatives |
| US6271377B1 (en) | 1999-02-25 | 2001-08-07 | Ciba Specialty Chemicals Corporation | Hydroxy-substituted N-alkoxy hindered amines and compositions stabilized therewith |
| NL1014465C2 (nl) | 1999-03-01 | 2002-01-29 | Ciba Sc Holding Ag | Stabilisatorcombinatie voor het rotomoldingproces. |
| US6444733B1 (en) * | 1999-03-01 | 2002-09-03 | Ciba Specialty Chemicals Corporation | Stabilizer combination for the rotomolding process |
| DE19929302A1 (de) * | 1999-06-25 | 2000-12-28 | Basf Ag | Haftfähigkeitsverringerte Formmassen für Kraftfahrzeuganwendungen |
| DE19948117A1 (de) | 1999-10-06 | 2001-04-12 | Basf Ag | Stabilisatorzusammensetzung |
| JP3717360B2 (ja) * | 2000-02-04 | 2005-11-16 | ナカシマプロペラ株式会社 | 人工関節用摺動部材の成形方法 |
| WO2002020508A1 (en) | 2000-08-23 | 2002-03-14 | Youngdae Kim | Polyoxyethylene-polyoxypropylene vitamin e and process for preparation thereof |
| CA2436960C (en) * | 2000-12-06 | 2012-08-07 | Ciba Specialty Chemicals Holding Inc. | Polypropylene resin compositions |
| DE10161863A1 (de) | 2001-12-14 | 2003-07-03 | Basf Ag | Stabilisatorzusammensetzung II |
| WO2003057772A2 (en) | 2001-12-27 | 2003-07-17 | Cytec Technology Corp. | Uv stabilized thermoplastic olefins |
| CN1302058C (zh) * | 2002-05-27 | 2007-02-28 | 大湖化学公司欧洲分公司 | 稳定化的聚丙烯 |
| WO2004024810A2 (en) | 2002-09-11 | 2004-03-25 | Ciba, Specialty Chemicals Holding Inc. | Stabillization of organic materials |
| JP2006501351A (ja) | 2002-10-01 | 2006-01-12 | エクソンモービル・ケミカル・パテンツ・インク | 回転成形用ポリエチレン組成物 |
| EP1308084A1 (en) | 2002-10-02 | 2003-05-07 | Ciba SC Holding AG | Synergistic UV absorber combination |
| DE10254548A1 (de) * | 2002-11-21 | 2004-06-17 | Basf Ag | Verwendung UV-Absorber enthaltender Polymerpulver zur Stabilisierung von Polymeren gegen die Einwirkung von UV-Strahlung |
| KR101114272B1 (ko) * | 2003-02-26 | 2012-03-28 | 시바 홀딩 인크 | 수 혼화성의 입체적으로 속박된 하이드록시 치환된 알콕시아민 |
| US20050081278A1 (en) * | 2003-10-17 | 2005-04-21 | Williams William A. | Polymeric glove with lotion coating and method of making same |
| US20070227087A1 (en) * | 2003-10-24 | 2007-10-04 | Crane Plastics Company Llc | Method of manufacturing simulated stone, brick, and masonry panels and wall structures |
| SA07280006B1 (ar) | 2006-02-01 | 2011-05-14 | سيبا سبشيالتي كيميكالز هولدينج انك | استخدام امينات ثنائية معاقة فراغياً كإضافات معالجة في عمليات التشكيل الدوراني |
| US8765848B2 (en) | 2006-03-16 | 2014-07-01 | Clariant Finance (Bvi) Limited | Modified waxes, a process for their preparation, and their use |
| WO2007128672A1 (en) * | 2006-05-03 | 2007-11-15 | Ciba Holding Inc. | Substituted hexahydro-1,4-diazepin-5-ones and compositions stabilized therewith |
| DK2118174T3 (da) | 2007-03-12 | 2013-02-25 | Bayer Oy | Anvendelse af tocopherol |
| ATE544476T1 (de) | 2007-04-10 | 2012-02-15 | Zimmer Inc | Antioxidans-stabilisiertes vernetztes ultrahochmolekulares polyethylen für anwendungen in medizinprodukten |
| EP2164892A1 (en) | 2007-07-10 | 2010-03-24 | Basf Se | Stabilizer compositions |
| EP2014704B1 (en) * | 2007-07-13 | 2010-12-15 | Borealis Technology Oy | Low migration polyolefin composition comprising vitamin E-type stabiliser |
| JP5411525B2 (ja) | 2009-02-18 | 2014-02-12 | 株式会社Ａｄｅｋａ | 耐熱性の改善された紫外線吸収剤組成物及びこれを含有してなる合成樹脂組成物 |
| DK2421913T3 (en) | 2009-04-21 | 2017-07-17 | Basf Corp | METHOD OF ROTATING POLYETHYLE ARTICLES |
| JP2010270310A (ja) * | 2009-04-24 | 2010-12-02 | Sumitomo Chemical Co Ltd | 安定剤組成物及び該組成物を含有する熱可塑性ポリマー組成物 |
| JP5177575B2 (ja) | 2010-01-28 | 2013-04-03 | 三菱電機株式会社 | 再生ポリオレフィン系樹脂組成物および再生ポリスチレン系樹脂組成物 |
| US11267951B2 (en) | 2010-12-13 | 2022-03-08 | Cytec Technology Corp. | Stabilizer compositions containing substituted chroman compounds and methods of use |
| NZ726849A (en) | 2012-06-13 | 2018-06-29 | Cytec Tech Corp | Stabilizer compositions containing substituted chroman compounds and methods of use |
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