JP2012515234A - 有機黒色顔料およびその製造 - Google Patents
有機黒色顔料およびその製造 Download PDFInfo
- Publication number
- JP2012515234A JP2012515234A JP2011545661A JP2011545661A JP2012515234A JP 2012515234 A JP2012515234 A JP 2012515234A JP 2011545661 A JP2011545661 A JP 2011545661A JP 2011545661 A JP2011545661 A JP 2011545661A JP 2012515234 A JP2012515234 A JP 2012515234A
- Authority
- JP
- Japan
- Prior art keywords
- formula
- ray powder
- lines
- molar ratio
- alkyl
- 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
Links
- 239000000049 pigment Substances 0.000 title claims abstract description 49
- 238000004519 manufacturing process Methods 0.000 title claims description 15
- 150000001875 compounds Chemical class 0.000 claims abstract description 101
- 239000003054 catalyst Substances 0.000 claims abstract description 84
- 239000003086 colorant Substances 0.000 claims abstract description 77
- 238000000034 method Methods 0.000 claims abstract description 71
- 239000000203 mixture Substances 0.000 claims abstract description 63
- 239000013078 crystal Substances 0.000 claims abstract description 50
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 42
- 230000008569 process Effects 0.000 claims abstract description 31
- 239000003973 paint Substances 0.000 claims abstract description 21
- 239000004611 light stabiliser Substances 0.000 claims abstract description 17
- 229920003023 plastic Polymers 0.000 claims abstract description 11
- 239000004033 plastic Substances 0.000 claims abstract description 11
- 239000000976 ink Substances 0.000 claims abstract description 8
- 238000007639 printing Methods 0.000 claims abstract description 8
- 239000000843 powder Substances 0.000 claims description 138
- 239000007795 chemical reaction product Substances 0.000 claims description 76
- 230000002378 acidificating effect Effects 0.000 claims description 74
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 claims description 74
- 125000000217 alkyl group Chemical group 0.000 claims description 72
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims description 66
- 238000006243 chemical reaction Methods 0.000 claims description 56
- 239000000047 product Substances 0.000 claims description 48
- 238000006555 catalytic reaction Methods 0.000 claims description 36
- 239000002245 particle Substances 0.000 claims description 36
- 229910052801 chlorine Inorganic materials 0.000 claims description 34
- 229910052731 fluorine Inorganic materials 0.000 claims description 28
- 229910052739 hydrogen Inorganic materials 0.000 claims description 27
- 229960000583 acetic acid Drugs 0.000 claims description 25
- 229910004013 NO 2 Inorganic materials 0.000 claims description 23
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 23
- 229910052799 carbon Inorganic materials 0.000 claims description 21
- 229910052794 bromium Inorganic materials 0.000 claims description 19
- 125000003545 alkoxy group Chemical group 0.000 claims description 18
- 239000000463 material Substances 0.000 claims description 17
- 125000000464 thioxo group Chemical group S=* 0.000 claims description 15
- 125000003342 alkenyl group Chemical group 0.000 claims description 13
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 13
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 12
- 125000000304 alkynyl group Chemical group 0.000 claims description 11
- 125000003118 aryl group Chemical group 0.000 claims description 11
- 229910052736 halogen Inorganic materials 0.000 claims description 11
- 125000006297 carbonyl amino group Chemical group [H]N([*:2])C([*:1])=O 0.000 claims description 10
- 125000000392 cycloalkenyl group Chemical group 0.000 claims description 9
- 239000012362 glacial acetic acid Substances 0.000 claims description 9
- 150000002367 halogens Chemical class 0.000 claims description 9
- 229910052757 nitrogen Inorganic materials 0.000 claims description 8
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 8
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 7
- 125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 claims description 7
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 claims description 6
- 150000001793 charged compounds Chemical class 0.000 claims description 6
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 6
- 125000001072 heteroaryl group Chemical group 0.000 claims description 6
- 229910052760 oxygen Inorganic materials 0.000 claims description 6
- 238000001953 recrystallisation Methods 0.000 claims description 6
- 229910052717 sulfur Inorganic materials 0.000 claims description 6
- 125000000592 heterocycloalkyl group Chemical group 0.000 claims description 5
- 101100079984 Caenorhabditis elegans nhr-9 gene Proteins 0.000 claims description 4
- 125000004450 alkenylene group Chemical group 0.000 claims description 4
- 125000002947 alkylene group Chemical group 0.000 claims description 4
- 238000001819 mass spectrum Methods 0.000 claims description 4
- 125000001424 substituent group Chemical group 0.000 claims description 4
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 3
- 238000004040 coloring Methods 0.000 claims description 3
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims description 2
- 230000035484 reaction time Effects 0.000 claims description 2
- 239000012779 reinforcing material Substances 0.000 claims description 2
- 125000005843 halogen group Chemical group 0.000 claims 2
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 claims 2
- UPJMWRYBLNHWQS-UHFFFAOYSA-N 4-methylbenzenesulfonic acid;toluene Chemical compound CC1=CC=CC=C1.CC1=CC=C(S(O)(=O)=O)C=C1 UPJMWRYBLNHWQS-UHFFFAOYSA-N 0.000 claims 1
- 241000790917 Dioxys <bee> Species 0.000 claims 1
- 239000004606 Fillers/Extenders Substances 0.000 claims 1
- 150000001336 alkenes Chemical class 0.000 claims 1
- 239000004744 fabric Substances 0.000 claims 1
- 239000006229 carbon black Substances 0.000 abstract description 9
- 239000004753 textile Substances 0.000 abstract description 2
- 230000002195 synergetic effect Effects 0.000 abstract 1
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 97
- -1 acidic or neutral Substances 0.000 description 83
- JXDYKVIHCLTXOP-UHFFFAOYSA-N isatin Chemical compound C1=CC=C2C(=O)C(=O)NC2=C1 JXDYKVIHCLTXOP-UHFFFAOYSA-N 0.000 description 63
- 239000000460 chlorine Substances 0.000 description 52
- 238000010586 diagram Methods 0.000 description 50
- 238000000634 powder X-ray diffraction Methods 0.000 description 32
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 28
- 235000011054 acetic acid Nutrition 0.000 description 16
- 239000012429 reaction media Substances 0.000 description 16
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 15
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 12
- MCLKERLHVBEZIW-UHFFFAOYSA-N 2-[4-(carboxymethyl)-2,5-dihydroxyphenyl]acetic acid Chemical compound OC(=O)CC1=CC(O)=C(CC(O)=O)C=C1O MCLKERLHVBEZIW-UHFFFAOYSA-N 0.000 description 10
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 10
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 10
- 239000011248 coating agent Substances 0.000 description 10
- 238000000576 coating method Methods 0.000 description 10
- KJIFKLIQANRMOU-UHFFFAOYSA-N oxidanium;4-methylbenzenesulfonate Chemical compound O.CC1=CC=C(S(O)(=O)=O)C=C1 KJIFKLIQANRMOU-UHFFFAOYSA-N 0.000 description 10
- 150000003839 salts Chemical class 0.000 description 10
- 239000007859 condensation product Substances 0.000 description 9
- 239000006185 dispersion Substances 0.000 description 9
- 239000011368 organic material Substances 0.000 description 9
- 239000000725 suspension Substances 0.000 description 9
- 239000002966 varnish Substances 0.000 description 9
- XHDJYQWGFIBCEP-UHFFFAOYSA-N 5-Chloro-1H-indole-2,3-dione Chemical compound ClC1=CC=C2NC(=O)C(=O)C2=C1 XHDJYQWGFIBCEP-UHFFFAOYSA-N 0.000 description 8
- 239000002253 acid Substances 0.000 description 8
- 239000007864 aqueous solution Substances 0.000 description 8
- 0 Nc1sc(C(C2OC2*2)=O)c2cc1 Chemical compound Nc1sc(C(C2OC2*2)=O)c2cc1 0.000 description 7
- 150000001412 amines Chemical class 0.000 description 7
- QRUDEWIWKLJBPS-UHFFFAOYSA-N benzotriazole Chemical compound C1=CC=C2N[N][N]C2=C1 QRUDEWIWKLJBPS-UHFFFAOYSA-N 0.000 description 7
- 239000012964 benzotriazole Substances 0.000 description 7
- JROGBPMEKVAPEH-GXGBFOEMSA-N emetine dihydrochloride Chemical compound Cl.Cl.N1CCC2=CC(OC)=C(OC)C=C2[C@H]1C[C@H]1C[C@H]2C3=CC(OC)=C(OC)C=C3CCN2C[C@@H]1CC JROGBPMEKVAPEH-GXGBFOEMSA-N 0.000 description 7
- 239000012071 phase Substances 0.000 description 7
- 239000004014 plasticizer Substances 0.000 description 7
- 229920000728 polyester Polymers 0.000 description 7
- 239000006104 solid solution Substances 0.000 description 7
- 239000002904 solvent Substances 0.000 description 7
- LBLYYCQCTBFVLH-UHFFFAOYSA-N 2-Methylbenzenesulfonic acid Chemical compound CC1=CC=CC=C1S(O)(=O)=O LBLYYCQCTBFVLH-UHFFFAOYSA-N 0.000 description 6
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 6
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 6
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 6
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 6
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 6
- 229920002678 cellulose Polymers 0.000 description 6
- 238000001035 drying Methods 0.000 description 6
- 238000010438 heat treatment Methods 0.000 description 6
- 230000007935 neutral effect Effects 0.000 description 6
- 229920005989 resin Polymers 0.000 description 6
- 239000011347 resin Substances 0.000 description 6
- IMFACGCPASFAPR-UHFFFAOYSA-N tributylamine Chemical class CCCCN(CCCC)CCCC IMFACGCPASFAPR-UHFFFAOYSA-N 0.000 description 6
- DMHGXMPXHPOXBF-UHFFFAOYSA-N 5-Methoxyisatin Chemical compound COC1=CC=C2NC(=O)C(=O)C2=C1 DMHGXMPXHPOXBF-UHFFFAOYSA-N 0.000 description 5
- UNMYHYODJHKLOC-UHFFFAOYSA-N 5-Nitroisatin Chemical compound [O-][N+](=O)C1=CC=C2NC(=O)C(=O)C2=C1 UNMYHYODJHKLOC-UHFFFAOYSA-N 0.000 description 5
- VAJCSPZKMVQIAP-UHFFFAOYSA-N 5-methyl-1h-indole-2,3-dione Chemical compound CC1=CC=C2NC(=O)C(=O)C2=C1 VAJCSPZKMVQIAP-UHFFFAOYSA-N 0.000 description 5
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 5
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 5
- 239000000654 additive Substances 0.000 description 5
- 229920000180 alkyd Polymers 0.000 description 5
- 239000002585 base Substances 0.000 description 5
- 230000015572 biosynthetic process Effects 0.000 description 5
- 239000001913 cellulose Substances 0.000 description 5
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 5
- 230000000694 effects Effects 0.000 description 5
- 239000001257 hydrogen Substances 0.000 description 5
- 238000005259 measurement Methods 0.000 description 5
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 5
- 239000011541 reaction mixture Substances 0.000 description 5
- 239000011780 sodium chloride Substances 0.000 description 5
- 239000000243 solution Substances 0.000 description 5
- 239000008096 xylene Substances 0.000 description 5
- RXFCIXRFAJRBSG-UHFFFAOYSA-N 3,2,3-tetramine Chemical compound NCCCNCCNCCCN RXFCIXRFAJRBSG-UHFFFAOYSA-N 0.000 description 4
- AYGGQJHJRFZDFH-UHFFFAOYSA-N 5,7-dichloro-1h-indole-2,3-dione Chemical compound ClC1=CC(Cl)=CC2=C1NC(=O)C2=O AYGGQJHJRFZDFH-UHFFFAOYSA-N 0.000 description 4
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 4
- 239000000020 Nitrocellulose Substances 0.000 description 4
- 230000008859 change Effects 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
- 125000004122 cyclic group Chemical group 0.000 description 4
- UKMSUNONTOPOIO-UHFFFAOYSA-N docosanoic acid Chemical compound CCCCCCCCCCCCCCCCCCCCCC(O)=O UKMSUNONTOPOIO-UHFFFAOYSA-N 0.000 description 4
- 150000002148 esters Chemical class 0.000 description 4
- 239000011521 glass Substances 0.000 description 4
- 125000004435 hydrogen atom Chemical class [H]* 0.000 description 4
- 239000005457 ice water Substances 0.000 description 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 4
- LQNUZADURLCDLV-UHFFFAOYSA-N nitrobenzene Chemical compound [O-][N+](=O)C1=CC=CC=C1 LQNUZADURLCDLV-UHFFFAOYSA-N 0.000 description 4
- 229920001220 nitrocellulos Polymers 0.000 description 4
- 229920000137 polyphosphoric acid Polymers 0.000 description 4
- 239000011343 solid material Substances 0.000 description 4
- 238000012360 testing method Methods 0.000 description 4
- ARXJGSRGQADJSQ-UHFFFAOYSA-N 1-methoxypropan-2-ol Chemical compound COCC(C)O ARXJGSRGQADJSQ-UHFFFAOYSA-N 0.000 description 3
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- HFZSCCJTJGWTDZ-UHFFFAOYSA-N 5,7-dimethyl-1h-indole-2,3-dione Chemical compound CC1=CC(C)=CC2=C1NC(=O)C2=O HFZSCCJTJGWTDZ-UHFFFAOYSA-N 0.000 description 3
- GKODDAXOSGGARJ-UHFFFAOYSA-N 5-Fluoroisatin Chemical compound FC1=CC=C2NC(=O)C(=O)C2=C1 GKODDAXOSGGARJ-UHFFFAOYSA-N 0.000 description 3
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 3
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 3
- ZZSNKZQZMQGXPY-UHFFFAOYSA-N Ethyl cellulose Chemical compound CCOCC1OC(OC)C(OCC)C(OCC)C1OC1C(O)C(O)C(OC)C(CO)O1 ZZSNKZQZMQGXPY-UHFFFAOYSA-N 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 3
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- 239000004594 Masterbatch (MB) Substances 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- 239000004698 Polyethylene Substances 0.000 description 3
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical group C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 3
- 235000021355 Stearic acid Nutrition 0.000 description 3
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 3
- 239000006096 absorbing agent Substances 0.000 description 3
- 238000010521 absorption reaction Methods 0.000 description 3
- 150000007513 acids Chemical class 0.000 description 3
- 238000012644 addition polymerization Methods 0.000 description 3
- 150000001408 amides Chemical class 0.000 description 3
- 239000006227 byproduct Substances 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- 238000000921 elemental analysis Methods 0.000 description 3
- 239000003623 enhancer Substances 0.000 description 3
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 3
- 239000012530 fluid Substances 0.000 description 3
- 239000011737 fluorine Substances 0.000 description 3
- 230000005484 gravity Effects 0.000 description 3
- 238000000227 grinding Methods 0.000 description 3
- UWNADWZGEHDQAB-UHFFFAOYSA-N i-Pr2C2H4i-Pr2 Natural products CC(C)CCC(C)C UWNADWZGEHDQAB-UHFFFAOYSA-N 0.000 description 3
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 3
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 3
- 239000008188 pellet Substances 0.000 description 3
- 229920000098 polyolefin Polymers 0.000 description 3
- 229920001451 polypropylene glycol Polymers 0.000 description 3
- 238000012545 processing Methods 0.000 description 3
- 239000008117 stearic acid Substances 0.000 description 3
- 239000000758 substrate Substances 0.000 description 3
- CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 description 3
- 239000001993 wax Substances 0.000 description 3
- UOCLXMDMGBRAIB-UHFFFAOYSA-N 1,1,1-trichloroethane Chemical compound CC(Cl)(Cl)Cl UOCLXMDMGBRAIB-UHFFFAOYSA-N 0.000 description 2
- DHKHKXVYLBGOIT-UHFFFAOYSA-N 1,1-Diethoxyethane Chemical compound CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 description 2
- JYEUMXHLPRZUAT-UHFFFAOYSA-N 1,2,3-triazine Chemical compound C1=CN=NN=C1 JYEUMXHLPRZUAT-UHFFFAOYSA-N 0.000 description 2
- KVZJLSYJROEPSQ-UHFFFAOYSA-N 1,2-dimethylcyclohexane Chemical compound CC1CCCCC1C KVZJLSYJROEPSQ-UHFFFAOYSA-N 0.000 description 2
- OCJBOOLMMGQPQU-UHFFFAOYSA-N 1,4-dichlorobenzene Chemical compound ClC1=CC=C(Cl)C=C1 OCJBOOLMMGQPQU-UHFFFAOYSA-N 0.000 description 2
- XCYJPXQACVEIOS-UHFFFAOYSA-N 1-isopropyl-3-methylbenzene Chemical compound CC(C)C1=CC=CC(C)=C1 XCYJPXQACVEIOS-UHFFFAOYSA-N 0.000 description 2
- BWJKLDGAAPQXGO-UHFFFAOYSA-N 2,2,6,6-tetramethyl-4-octadecoxypiperidine Chemical compound CCCCCCCCCCCCCCCCCCOC1CC(C)(C)NC(C)(C)C1 BWJKLDGAAPQXGO-UHFFFAOYSA-N 0.000 description 2
- ONTODYXHFBKCDK-UHFFFAOYSA-N 2-(2,4-dimethylphenyl)-1,3,5-triazine Chemical compound CC1=CC(C)=CC=C1C1=NC=NC=N1 ONTODYXHFBKCDK-UHFFFAOYSA-N 0.000 description 2
- SBASXUCJHJRPEV-UHFFFAOYSA-N 2-(2-methoxyethoxy)ethanol Chemical compound COCCOCCO SBASXUCJHJRPEV-UHFFFAOYSA-N 0.000 description 2
- XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 description 2
- MSXVEPNJUHWQHW-UHFFFAOYSA-N 2-methylbutan-2-ol Chemical compound CCC(C)(C)O MSXVEPNJUHWQHW-UHFFFAOYSA-N 0.000 description 2
- SVTBMSDMJJWYQN-UHFFFAOYSA-N 2-methylpentane-2,4-diol Chemical compound CC(O)CC(C)(C)O SVTBMSDMJJWYQN-UHFFFAOYSA-N 0.000 description 2
- 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 description 2
- FBIXXCXCZOZFCO-UHFFFAOYSA-N 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 FBIXXCXCZOZFCO-UHFFFAOYSA-N 0.000 description 2
- BVNWQSXXRMNYKH-UHFFFAOYSA-N 4-phenyl-2h-benzotriazole Chemical compound C1=CC=CC=C1C1=CC=CC2=C1NN=N2 BVNWQSXXRMNYKH-UHFFFAOYSA-N 0.000 description 2
- MBVCESWADCIXJN-UHFFFAOYSA-N 5-Bromoisatin Chemical compound BrC1=CC=C2NC(=O)C(=O)C2=C1 MBVCESWADCIXJN-UHFFFAOYSA-N 0.000 description 2
- DLFVBJFMPXGRIB-UHFFFAOYSA-N Acetamide Chemical compound CC(N)=O DLFVBJFMPXGRIB-UHFFFAOYSA-N 0.000 description 2
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- 235000021357 Behenic acid Nutrition 0.000 description 2
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
- LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 description 2
- SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 2
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 2
- 239000001856 Ethyl cellulose Substances 0.000 description 2
- ZHNUHDYFZUAESO-UHFFFAOYSA-N Formamide Chemical compound NC=O ZHNUHDYFZUAESO-UHFFFAOYSA-N 0.000 description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- 229920000877 Melamine resin Polymers 0.000 description 2
- ATHHXGZTWNVVOU-UHFFFAOYSA-N N-methylformamide Chemical compound CNC=O ATHHXGZTWNVVOU-UHFFFAOYSA-N 0.000 description 2
- REYJJPSVUYRZGE-UHFFFAOYSA-N Octadecylamine Chemical compound CCCCCCCCCCCCCCCCCCN REYJJPSVUYRZGE-UHFFFAOYSA-N 0.000 description 2
- CYTYCFOTNPOANT-UHFFFAOYSA-N Perchloroethylene Chemical group ClC(Cl)=C(Cl)Cl CYTYCFOTNPOANT-UHFFFAOYSA-N 0.000 description 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- 239000002202 Polyethylene glycol Substances 0.000 description 2
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 2
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 2
- DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- FZWLAAWBMGSTSO-UHFFFAOYSA-N Thiazole Chemical group C1=CSC=N1 FZWLAAWBMGSTSO-UHFFFAOYSA-N 0.000 description 2
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 229910001860 alkaline earth metal hydroxide Inorganic materials 0.000 description 2
- RDOXTESZEPMUJZ-UHFFFAOYSA-N anisole Chemical compound COC1=CC=CC=C1 RDOXTESZEPMUJZ-UHFFFAOYSA-N 0.000 description 2
- 239000012752 auxiliary agent Substances 0.000 description 2
- 229940116226 behenic acid Drugs 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- BTANRVKWQNVYAZ-UHFFFAOYSA-N butan-2-ol Chemical compound CCC(C)O BTANRVKWQNVYAZ-UHFFFAOYSA-N 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 2
- 238000007385 chemical modification Methods 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- NNBZCPXTIHJBJL-UHFFFAOYSA-N decalin Chemical compound C1CCCC2CCCCC21 NNBZCPXTIHJBJL-UHFFFAOYSA-N 0.000 description 2
- 229940117389 dichlorobenzene Drugs 0.000 description 2
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 2
- 238000009826 distribution Methods 0.000 description 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 description 2
- JRBPAEWTRLWTQC-UHFFFAOYSA-N dodecylamine Chemical compound CCCCCCCCCCCCN JRBPAEWTRLWTQC-UHFFFAOYSA-N 0.000 description 2
- 229920001971 elastomer Polymers 0.000 description 2
- 238000000119 electrospray ionisation mass spectrum Methods 0.000 description 2
- JBKVHLHDHHXQEQ-UHFFFAOYSA-N epsilon-caprolactam Chemical compound O=C1CCCCCN1 JBKVHLHDHHXQEQ-UHFFFAOYSA-N 0.000 description 2
- 150000002170 ethers Chemical class 0.000 description 2
- 229920001249 ethyl cellulose Polymers 0.000 description 2
- 235000019325 ethyl cellulose Nutrition 0.000 description 2
- FKRCODPIKNYEAC-UHFFFAOYSA-N ethyl propionate Chemical compound CCOC(=O)CC FKRCODPIKNYEAC-UHFFFAOYSA-N 0.000 description 2
- IIEWJVIFRVWJOD-UHFFFAOYSA-N ethylcyclohexane Chemical compound CCC1CCCCC1 IIEWJVIFRVWJOD-UHFFFAOYSA-N 0.000 description 2
- 239000000945 filler Substances 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 description 2
- KQNPFQTWMSNSAP-UHFFFAOYSA-N isobutyric acid Chemical compound CC(C)C(O)=O KQNPFQTWMSNSAP-UHFFFAOYSA-N 0.000 description 2
- 238000004898 kneading Methods 0.000 description 2
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 2
- 150000002605 large molecules Chemical class 0.000 description 2
- 229920000092 linear low density polyethylene Polymers 0.000 description 2
- 239000004707 linear low-density polyethylene Substances 0.000 description 2
- 238000011068 loading method Methods 0.000 description 2
- HQKMJHAJHXVSDF-UHFFFAOYSA-L magnesium stearate Chemical compound [Mg+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O HQKMJHAJHXVSDF-UHFFFAOYSA-L 0.000 description 2
- 238000000816 matrix-assisted laser desorption--ionisation Methods 0.000 description 2
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
- BHIWKHZACMWKOJ-UHFFFAOYSA-N methyl isobutyrate Chemical compound COC(=O)C(C)C BHIWKHZACMWKOJ-UHFFFAOYSA-N 0.000 description 2
- UAEPNZWRGJTJPN-UHFFFAOYSA-N methylcyclohexane Chemical compound CC1CCCCC1 UAEPNZWRGJTJPN-UHFFFAOYSA-N 0.000 description 2
- 229910003455 mixed metal oxide Inorganic materials 0.000 description 2
- 125000001421 myristyl 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])[H] 0.000 description 2
- 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 description 2
- 125000001280 n-hexyl group Chemical group C(CCCCC)* 0.000 description 2
- 238000006386 neutralization reaction Methods 0.000 description 2
- GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 description 2
- LYRFLYHAGKPMFH-UHFFFAOYSA-N octadecanamide Chemical compound CCCCCCCCCCCCCCCCCC(N)=O LYRFLYHAGKPMFH-UHFFFAOYSA-N 0.000 description 2
- HFPZCAJZSCWRBC-UHFFFAOYSA-N p-cymene Chemical compound CC(C)C1=CC=C(C)C=C1 HFPZCAJZSCWRBC-UHFFFAOYSA-N 0.000 description 2
- 125000003538 pentan-3-yl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])C([H])([H])[H] 0.000 description 2
- 230000002093 peripheral effect Effects 0.000 description 2
- 239000003208 petroleum Substances 0.000 description 2
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 2
- 230000019612 pigmentation Effects 0.000 description 2
- 229920001610 polycaprolactone Polymers 0.000 description 2
- 239000004632 polycaprolactone Substances 0.000 description 2
- 238000012643 polycondensation polymerization Methods 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- 229920001223 polyethylene glycol Polymers 0.000 description 2
- 229940068886 polyethylene glycol 300 Drugs 0.000 description 2
- 239000002861 polymer material Substances 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 2
- YKYONYBAUNKHLG-UHFFFAOYSA-N propyl acetate Chemical compound CCCOC(C)=O YKYONYBAUNKHLG-UHFFFAOYSA-N 0.000 description 2
- 230000005855 radiation Effects 0.000 description 2
- 239000000376 reactant Substances 0.000 description 2
- 239000005060 rubber Substances 0.000 description 2
- 229920006395 saturated elastomer Polymers 0.000 description 2
- CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 2
- 150000003335 secondary amines Chemical class 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000003549 soybean oil Substances 0.000 description 2
- 235000012424 soybean oil Nutrition 0.000 description 2
- 230000003595 spectral effect Effects 0.000 description 2
- 238000005507 spraying Methods 0.000 description 2
- 239000003381 stabilizer Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 238000006467 substitution reaction Methods 0.000 description 2
- 238000006277 sulfonation reaction Methods 0.000 description 2
- 238000003786 synthesis reaction Methods 0.000 description 2
- YTZKOQUCBOVLHL-UHFFFAOYSA-N tert-butylbenzene Chemical compound CC(C)(C)C1=CC=CC=C1 YTZKOQUCBOVLHL-UHFFFAOYSA-N 0.000 description 2
- 150000003512 tertiary amines Chemical class 0.000 description 2
- 229950011008 tetrachloroethylene Drugs 0.000 description 2
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 2
- UMGDCJDMYOKAJW-UHFFFAOYSA-N thiourea Chemical compound NC(N)=S UMGDCJDMYOKAJW-UHFFFAOYSA-N 0.000 description 2
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 2
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 2
- 238000012546 transfer Methods 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- DTGKSKDOIYIVQL-WEDXCCLWSA-N (+)-borneol Chemical group C1C[C@@]2(C)[C@@H](O)C[C@@H]1C2(C)C DTGKSKDOIYIVQL-WEDXCCLWSA-N 0.000 description 1
- PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 description 1
- 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 description 1
- OBETXYAYXDNJHR-SSDOTTSWSA-M (2r)-2-ethylhexanoate Chemical compound CCCC[C@@H](CC)C([O-])=O OBETXYAYXDNJHR-SSDOTTSWSA-M 0.000 description 1
- JJYUJOJVFRXHAE-UHFFFAOYSA-N (3,5,5-trimethyl-6-oxomorpholin-3-yl)methyl 2-ethylhexanoate Chemical compound CCCCC(CC)C(=O)OCC1(C)COC(=O)C(C)(C)N1 JJYUJOJVFRXHAE-UHFFFAOYSA-N 0.000 description 1
- MHCVCKDNQYMGEX-UHFFFAOYSA-N 1,1'-biphenyl;phenoxybenzene Chemical compound C1=CC=CC=C1C1=CC=CC=C1.C=1C=CC=CC=1OC1=CC=CC=C1 MHCVCKDNQYMGEX-UHFFFAOYSA-N 0.000 description 1
- SCYULBFZEHDVBN-UHFFFAOYSA-N 1,1-Dichloroethane Chemical compound CC(Cl)Cl SCYULBFZEHDVBN-UHFFFAOYSA-N 0.000 description 1
- YAXWOADCWUUUNX-UHFFFAOYSA-N 1,2,2,3-tetramethylpiperidine Chemical compound CC1CCCN(C)C1(C)C YAXWOADCWUUUNX-UHFFFAOYSA-N 0.000 description 1
- CGXOAAMIQPDTPE-UHFFFAOYSA-N 1,2,2,6,6-pentamethylpiperidin-4-amine Chemical compound CN1C(C)(C)CC(N)CC1(C)C CGXOAAMIQPDTPE-UHFFFAOYSA-N 0.000 description 1
- RELMFMZEBKVZJC-UHFFFAOYSA-N 1,2,3-trichlorobenzene Chemical compound ClC1=CC=CC(Cl)=C1Cl RELMFMZEBKVZJC-UHFFFAOYSA-N 0.000 description 1
- ZWVMLYRJXORSEP-UHFFFAOYSA-N 1,2,6-Hexanetriol Chemical compound OCCCCC(O)CO ZWVMLYRJXORSEP-UHFFFAOYSA-N 0.000 description 1
- BSKLHRVHTUTEBF-UHFFFAOYSA-N 1,2-diethoxyethane;1,2-dimethoxyethane Chemical compound COCCOC.CCOCCOCC BSKLHRVHTUTEBF-UHFFFAOYSA-N 0.000 description 1
- CYSGHNMQYZDMIA-UHFFFAOYSA-N 1,3-Dimethyl-2-imidazolidinon Chemical compound CN1CCN(C)C1=O CYSGHNMQYZDMIA-UHFFFAOYSA-N 0.000 description 1
- KEQGZUUPPQEDPF-UHFFFAOYSA-N 1,3-dichloro-5,5-dimethylimidazolidine-2,4-dione Chemical compound CC1(C)N(Cl)C(=O)N(Cl)C1=O KEQGZUUPPQEDPF-UHFFFAOYSA-N 0.000 description 1
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- FLOFHDFTDMRWIW-UHFFFAOYSA-N 1,4-dimethylindole-2,3-dione Chemical compound C1=CC=C(C)C2=C1N(C)C(=O)C2=O FLOFHDFTDMRWIW-UHFFFAOYSA-N 0.000 description 1
- 229940043375 1,5-pentanediol Drugs 0.000 description 1
- WWRCMNKATXZARA-UHFFFAOYSA-N 1-Isopropyl-2-methylbenzene Chemical compound CC(C)C1=CC=CC=C1C WWRCMNKATXZARA-UHFFFAOYSA-N 0.000 description 1
- KKOFPMFUCMGHDX-UHFFFAOYSA-N 1-[[3,5-bis[cyclohexyl-(3,3,4,5,5-pentamethyl-2-oxopiperazin-1-yl)amino]-1,3,5-triazinan-1-yl]-cyclohexylamino]-3,3,4,5,5-pentamethylpiperazin-2-one Chemical compound O=C1C(C)(C)N(C)C(C)(C)CN1N(N1CN(CN(C1)N(C1CCCCC1)N1C(C(C)(C)N(C)C(C)(C)C1)=O)N(C1CCCCC1)N1C(C(C)(C)N(C)C(C)(C)C1)=O)C1CCCCC1 KKOFPMFUCMGHDX-UHFFFAOYSA-N 0.000 description 1
- MESWESDXDWUFHK-UHFFFAOYSA-N 1-[[3,5-bis[cyclohexyl-(3,3,5,5-tetramethyl-2-oxopiperazin-1-yl)amino]-1,3,5-triazinan-1-yl]-cyclohexylamino]-3,3,5,5-tetramethylpiperazin-2-one Chemical compound O=C1C(C)(C)NC(C)(C)CN1N(N1CN(CN(C1)N(C1CCCCC1)N1C(C(C)(C)NC(C)(C)C1)=O)N(C1CCCCC1)N1C(C(C)(C)NC(C)(C)C1)=O)C1CCCCC1 MESWESDXDWUFHK-UHFFFAOYSA-N 0.000 description 1
- DURPTKYDGMDSBL-UHFFFAOYSA-N 1-butoxybutane Chemical compound CCCCOCCCC DURPTKYDGMDSBL-UHFFFAOYSA-N 0.000 description 1
- ZGPFGHSOYPBCGI-UHFFFAOYSA-N 1-chloroindole-2,3-dione Chemical compound C1=CC=C2N(Cl)C(=O)C(=O)C2=C1 ZGPFGHSOYPBCGI-UHFFFAOYSA-N 0.000 description 1
- VCYBVWFTGAZHGH-UHFFFAOYSA-N 1-methylindole-2,3-dione Chemical compound C1=CC=C2N(C)C(=O)C(=O)C2=C1 VCYBVWFTGAZHGH-UHFFFAOYSA-N 0.000 description 1
- BAUWRHPMUVYFOD-UHFFFAOYSA-N 1-methylpiperidin-4-ol Chemical compound CN1CCC(O)CC1 BAUWRHPMUVYFOD-UHFFFAOYSA-N 0.000 description 1
- UWCPWBIMRYXUOU-UHFFFAOYSA-N 1-phenylindole-2,3-dione Chemical compound C12=CC=CC=C2C(=O)C(=O)N1C1=CC=CC=C1 UWCPWBIMRYXUOU-UHFFFAOYSA-N 0.000 description 1
- HFZLSTDPRQSZCQ-UHFFFAOYSA-N 1-pyrrolidin-3-ylpyrrolidine Chemical compound C1CCCN1C1CNCC1 HFZLSTDPRQSZCQ-UHFFFAOYSA-N 0.000 description 1
- 238000005160 1H NMR spectroscopy Methods 0.000 description 1
- NBUKAOOFKZFCGD-UHFFFAOYSA-N 2,2,3,3-tetrafluoropropan-1-ol Chemical compound OCC(F)(F)C(F)F NBUKAOOFKZFCGD-UHFFFAOYSA-N 0.000 description 1
- RKMGAJGJIURJSJ-UHFFFAOYSA-N 2,2,6,6-Tetramethylpiperidine Substances CC1(C)CCCC(C)(C)N1 RKMGAJGJIURJSJ-UHFFFAOYSA-N 0.000 description 1
- ROODQCZSWXEDJL-UHFFFAOYSA-N 2,3-dioxo-1h-indole-7-carboxylic acid Chemical compound OC(=O)C1=CC=CC2=C1NC(=O)C2=O ROODQCZSWXEDJL-UHFFFAOYSA-N 0.000 description 1
- HBQUOLGAXBYZGR-UHFFFAOYSA-N 2,4,6-triphenyl-1,3,5-triazine Chemical compound C1=CC=CC=C1C1=NC(C=2C=CC=CC=2)=NC(C=2C=CC=CC=2)=N1 HBQUOLGAXBYZGR-UHFFFAOYSA-N 0.000 description 1
- UCJDCGANFAKTKA-UHFFFAOYSA-N 2,4-dimethyl-1,3,5-triazine Chemical compound CC1=NC=NC(C)=N1 UCJDCGANFAKTKA-UHFFFAOYSA-N 0.000 description 1
- HWRLEEPNFJNTOP-UHFFFAOYSA-N 2-(1,3,5-triazin-2-yl)phenol Chemical compound OC1=CC=CC=C1C1=NC=NC=N1 HWRLEEPNFJNTOP-UHFFFAOYSA-N 0.000 description 1
- UUINYPIVWRZHAG-UHFFFAOYSA-N 2-(4,6-diphenyl-1,3,5-triazin-2-yl)-5-methoxyphenol Chemical compound OC1=CC(OC)=CC=C1C1=NC(C=2C=CC=CC=2)=NC(C=2C=CC=CC=2)=N1 UUINYPIVWRZHAG-UHFFFAOYSA-N 0.000 description 1
- ZMWRRFHBXARRRT-UHFFFAOYSA-N 2-(benzotriazol-2-yl)-4,6-bis(2-methylbutan-2-yl)phenol Chemical compound CCC(C)(C)C1=CC(C(C)(C)CC)=CC(N2N=C3C=CC=CC3=N2)=C1O ZMWRRFHBXARRRT-UHFFFAOYSA-N 0.000 description 1
- OLFNXLXEGXRUOI-UHFFFAOYSA-N 2-(benzotriazol-2-yl)-4,6-bis(2-phenylpropan-2-yl)phenol Chemical compound C=1C(N2N=C3C=CC=CC3=N2)=C(O)C(C(C)(C)C=2C=CC=CC=2)=CC=1C(C)(C)C1=CC=CC=C1 OLFNXLXEGXRUOI-UHFFFAOYSA-N 0.000 description 1
- IYAZLDLPUNDVAG-UHFFFAOYSA-N 2-(benzotriazol-2-yl)-4-(2,4,4-trimethylpentan-2-yl)phenol Chemical compound CC(C)(C)CC(C)(C)C1=CC=C(O)C(N2N=C3C=CC=CC3=N2)=C1 IYAZLDLPUNDVAG-UHFFFAOYSA-N 0.000 description 1
- WXHVQMGINBSVAY-UHFFFAOYSA-N 2-(benzotriazol-2-yl)-4-tert-butylphenol Chemical compound CC(C)(C)C1=CC=C(O)C(N2N=C3C=CC=CC3=N2)=C1 WXHVQMGINBSVAY-UHFFFAOYSA-N 0.000 description 1
- RTNVDKBRTXEWQE-UHFFFAOYSA-N 2-(benzotriazol-2-yl)-6-butan-2-yl-4-tert-butylphenol Chemical compound CCC(C)C1=CC(C(C)(C)C)=CC(N2N=C3C=CC=CC3=N2)=C1O RTNVDKBRTXEWQE-UHFFFAOYSA-N 0.000 description 1
- VQMHSKWEJGIXGA-UHFFFAOYSA-N 2-(benzotriazol-2-yl)-6-dodecyl-4-methylphenol Chemical compound CCCCCCCCCCCCC1=CC(C)=CC(N2N=C3C=CC=CC3=N2)=C1O VQMHSKWEJGIXGA-UHFFFAOYSA-N 0.000 description 1
- FJGQBLRYBUAASW-UHFFFAOYSA-N 2-(benzotriazol-2-yl)phenol Chemical compound OC1=CC=CC=C1N1N=C2C=CC=CC2=N1 FJGQBLRYBUAASW-UHFFFAOYSA-N 0.000 description 1
- WFSMVVDJSNMRAR-UHFFFAOYSA-N 2-[2-(2-ethoxyethoxy)ethoxy]ethanol Chemical compound CCOCCOCCOCCO WFSMVVDJSNMRAR-UHFFFAOYSA-N 0.000 description 1
- LCZVSXRMYJUNFX-UHFFFAOYSA-N 2-[2-(2-hydroxypropoxy)propoxy]propan-1-ol Chemical compound CC(O)COC(C)COC(C)CO LCZVSXRMYJUNFX-UHFFFAOYSA-N 0.000 description 1
- ONABRCKXKDSXCA-UHFFFAOYSA-N 2-[3-amino-2,6-bis[butyl-(1-cyclohexyloxy-2,2,6,6-tetramethylpiperidin-4-yl)amino]-2h-1,3,5-triazin-4-yl]ethanol Chemical compound N1=C(N(CCCC)C2CC(C)(C)N(OC3CCCCC3)C(C)(C)C2)N=C(CCO)N(N)C1N(CCCC)C(CC1(C)C)CC(C)(C)N1OC1CCCCC1 ONABRCKXKDSXCA-UHFFFAOYSA-N 0.000 description 1
- FESJNIGBEZWAIB-UHFFFAOYSA-N 2-[4,6-bis(2,4-dimethylphenyl)-1,3,5-triazin-2-yl]-5-(2-hydroxy-3-octoxypropoxy)phenol Chemical compound OC1=CC(OCC(O)COCCCCCCCC)=CC=C1C1=NC(C=2C(=CC(C)=CC=2)C)=NC(C=2C(=CC(C)=CC=2)C)=N1 FESJNIGBEZWAIB-UHFFFAOYSA-N 0.000 description 1
- SITYOOWCYAYOKL-UHFFFAOYSA-N 2-[4,6-bis(2,4-dimethylphenyl)-1,3,5-triazin-2-yl]-5-(3-dodecoxy-2-hydroxypropoxy)phenol Chemical compound OC1=CC(OCC(O)COCCCCCCCCCCCC)=CC=C1C1=NC(C=2C(=CC(C)=CC=2)C)=NC(C=2C(=CC(C)=CC=2)C)=N1 SITYOOWCYAYOKL-UHFFFAOYSA-N 0.000 description 1
- ZSSVCEUEVMALRD-UHFFFAOYSA-N 2-[4,6-bis(2,4-dimethylphenyl)-1,3,5-triazin-2-yl]-5-(octyloxy)phenol Chemical compound OC1=CC(OCCCCCCCC)=CC=C1C1=NC(C=2C(=CC(C)=CC=2)C)=NC(C=2C(=CC(C)=CC=2)C)=N1 ZSSVCEUEVMALRD-UHFFFAOYSA-N 0.000 description 1
- DBYBHKQEHCYBQV-UHFFFAOYSA-N 2-[4,6-bis(2,4-dimethylphenyl)-1,3,5-triazin-2-yl]-5-dodecoxyphenol Chemical compound OC1=CC(OCCCCCCCCCCCC)=CC=C1C1=NC(C=2C(=CC(C)=CC=2)C)=NC(C=2C(=CC(C)=CC=2)C)=N1 DBYBHKQEHCYBQV-UHFFFAOYSA-N 0.000 description 1
- LSNNLZXIHSJCIE-UHFFFAOYSA-N 2-[4,6-bis(2,4-dimethylphenyl)-1,3,5-triazin-2-yl]-5-tridecoxyphenol Chemical compound OC1=CC(OCCCCCCCCCCCCC)=CC=C1C1=NC(C=2C(=CC(C)=CC=2)C)=NC(C=2C(=CC(C)=CC=2)C)=N1 LSNNLZXIHSJCIE-UHFFFAOYSA-N 0.000 description 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 description 1
- NPUPWUDXQCOMBF-UHFFFAOYSA-N 2-[4,6-bis(4-methylphenyl)-1,3,5-triazin-2-yl]-5-octoxyphenol Chemical compound OC1=CC(OCCCCCCCC)=CC=C1C1=NC(C=2C=CC(C)=CC=2)=NC(C=2C=CC(C)=CC=2)=N1 NPUPWUDXQCOMBF-UHFFFAOYSA-N 0.000 description 1
- PIGBIZGGEUNVCV-UHFFFAOYSA-N 2-[4,6-bis[4-(3-butoxy-2-hydroxypropoxy)-2-hydroxyphenyl]-1,3,5-triazin-2-yl]-5-(3-butoxy-2-hydroxypropoxy)phenol Chemical compound OC1=CC(OCC(O)COCCCC)=CC=C1C1=NC(C=2C(=CC(OCC(O)COCCCC)=CC=2)O)=NC(C=2C(=CC(OCC(O)COCCCC)=CC=2)O)=N1 PIGBIZGGEUNVCV-UHFFFAOYSA-N 0.000 description 1
- HHIVRACNDKRDTF-UHFFFAOYSA-N 2-[4-(2,4-dimethylphenyl)-6-(2-hydroxy-4-propoxyphenyl)-1,3,5-triazin-2-yl]-5-propoxyphenol Chemical compound OC1=CC(OCCC)=CC=C1C1=NC(C=2C(=CC(C)=CC=2)C)=NC(C=2C(=CC(OCCC)=CC=2)O)=N1 HHIVRACNDKRDTF-UHFFFAOYSA-N 0.000 description 1
- VARDNKCBWBOEBW-UHFFFAOYSA-N 2-[4-(4-methoxyphenyl)-6-phenyl-1,3,5-triazin-2-yl]phenol Chemical compound C1=CC(OC)=CC=C1C1=NC(C=2C=CC=CC=2)=NC(C=2C(=CC=CC=2)O)=N1 VARDNKCBWBOEBW-UHFFFAOYSA-N 0.000 description 1
- DOTYDHBOKPPXRB-UHFFFAOYSA-N 2-butyl-2-[(3,5-ditert-butyl-4-hydroxyphenyl)methyl]propanedioic acid Chemical compound CCCCC(C(O)=O)(C(O)=O)CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 DOTYDHBOKPPXRB-UHFFFAOYSA-N 0.000 description 1
- 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 description 1
- ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 description 1
- 229940093475 2-ethoxyethanol Drugs 0.000 description 1
- LHHLLQVLJAUUDT-UHFFFAOYSA-N 2-ethylhexyl 3-[3-(benzotriazol-2-yl)-5-tert-butyl-4-hydroxyphenyl]propanoate Chemical compound CC(C)(C)C1=CC(CCC(=O)OCC(CC)CCCC)=CC(N2N=C3C=CC=CC3=N2)=C1O LHHLLQVLJAUUDT-UHFFFAOYSA-N 0.000 description 1
- AWEVLIFGIMIQHY-UHFFFAOYSA-N 2-ethylhexyl 3-[3-tert-butyl-5-(5-chlorobenzotriazol-2-yl)-4-hydroxyphenyl]propanoate Chemical compound CC(C)(C)C1=CC(CCC(=O)OCC(CC)CCCC)=CC(N2N=C3C=C(Cl)C=CC3=N2)=C1O AWEVLIFGIMIQHY-UHFFFAOYSA-N 0.000 description 1
- 125000002941 2-furyl group Chemical group O1C([*])=C([H])C([H])=C1[H] 0.000 description 1
- VNJOEUSYAMPBAK-UHFFFAOYSA-N 2-methylbenzenesulfonic acid;hydrate Chemical compound O.CC1=CC=CC=C1S(O)(=O)=O VNJOEUSYAMPBAK-UHFFFAOYSA-N 0.000 description 1
- 125000004493 2-methylbut-1-yl group Chemical group CC(C*)CC 0.000 description 1
- QHTJSSMHBLGUHV-UHFFFAOYSA-N 2-methylbutan-2-ylbenzene Chemical compound CCC(C)(C)C1=CC=CC=C1 QHTJSSMHBLGUHV-UHFFFAOYSA-N 0.000 description 1
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
- 125000004105 2-pyridyl group Chemical group N1=C([*])C([H])=C([H])C([H])=C1[H] 0.000 description 1
- 125000000175 2-thienyl group Chemical group S1C([*])=C([H])C([H])=C1[H] 0.000 description 1
- GUCMKIKYKIHUTM-UHFFFAOYSA-N 3,3,5,5-tetramethyl-1-[2-(3,3,5,5-tetramethyl-2-oxopiperazin-1-yl)ethyl]piperazin-2-one Chemical compound O=C1C(C)(C)NC(C)(C)CN1CCN1C(=O)C(C)(C)NC(C)(C)C1 GUCMKIKYKIHUTM-UHFFFAOYSA-N 0.000 description 1
- BTXXTMOWISPQSJ-UHFFFAOYSA-N 4,4,4-trifluorobutan-2-one Chemical compound CC(=O)CC(F)(F)F BTXXTMOWISPQSJ-UHFFFAOYSA-N 0.000 description 1
- 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 description 1
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 1
- UQAMDAUJTXFNAD-UHFFFAOYSA-N 4-(4,6-dichloro-1,3,5-triazin-2-yl)morpholine Chemical compound ClC1=NC(Cl)=NC(N2CCOCC2)=N1 UQAMDAUJTXFNAD-UHFFFAOYSA-N 0.000 description 1
- FROCQMFXPIROOK-UHFFFAOYSA-N 4-[4,6-bis(2,4-dimethylphenyl)-1,3,5-triazin-2-yl]benzene-1,3-diol Chemical compound CC1=CC(C)=CC=C1C1=NC(C=2C(=CC(C)=CC=2)C)=NC(C=2C(=CC(O)=CC=2)O)=N1 FROCQMFXPIROOK-UHFFFAOYSA-N 0.000 description 1
- XDPKOJHXFUVOLC-UHFFFAOYSA-N 4-hexadecoxy-2,2,6,6-tetramethylpiperidine Chemical compound CCCCCCCCCCCCCCCCOC1CC(C)(C)NC(C)(C)C1 XDPKOJHXFUVOLC-UHFFFAOYSA-N 0.000 description 1
- UWSMKYBKUPAEJQ-UHFFFAOYSA-N 5-Chloro-2-(3,5-di-tert-butyl-2-hydroxyphenyl)-2H-benzotriazole Chemical compound CC(C)(C)C1=CC(C(C)(C)C)=CC(N2N=C3C=C(Cl)C=CC3=N2)=C1O UWSMKYBKUPAEJQ-UHFFFAOYSA-N 0.000 description 1
- LDFQLYHDZZPAGN-UHFFFAOYSA-N 5-chloro-7-methyl-1h-indole-2,3-dione Chemical compound CC1=CC(Cl)=CC2=C1NC(=O)C2=O LDFQLYHDZZPAGN-UHFFFAOYSA-N 0.000 description 1
- IPRLZACALWPEGS-UHFFFAOYSA-N 7,7,9,9-tetramethyl-2-undecyl-1-oxa-3,8-diazaspiro[4.5]decan-4-one Chemical compound O1C(CCCCCCCCCCC)NC(=O)C11CC(C)(C)NC(C)(C)C1 IPRLZACALWPEGS-UHFFFAOYSA-N 0.000 description 1
- RAZWNFJQEZAVOT-UHFFFAOYSA-N 8-acetyl-3-dodecyl-7,7,9,9-tetramethyl-1,3,8-triazaspiro[4.5]decane-2,4-dione Chemical compound O=C1N(CCCCCCCCCCCC)C(=O)NC11CC(C)(C)N(C(C)=O)C(C)(C)C1 RAZWNFJQEZAVOT-UHFFFAOYSA-N 0.000 description 1
- LPEKGGXMPWTOCB-UHFFFAOYSA-N 8beta-(2,3-epoxy-2-methylbutyryloxy)-14-acetoxytithifolin Natural products COC(=O)C(C)O LPEKGGXMPWTOCB-UHFFFAOYSA-N 0.000 description 1
- BQACOLQNOUYJCE-FYZZASKESA-N Abietic acid Natural products CC(C)C1=CC2=CC[C@]3(C)[C@](C)(CCC[C@@]3(C)C(=O)O)[C@H]2CC1 BQACOLQNOUYJCE-FYZZASKESA-N 0.000 description 1
- QZCLKYGREBVARF-UHFFFAOYSA-N Acetyl tributyl citrate Chemical compound CCCCOC(=O)CC(C(=O)OCCCC)(OC(C)=O)CC(=O)OCCCC QZCLKYGREBVARF-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 1
- 229920000178 Acrylic resin Polymers 0.000 description 1
- 239000004925 Acrylic resin Substances 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- DKPFZGUDAPQIHT-UHFFFAOYSA-N Butyl acetate Natural products CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 1
- 125000000739 C2-C30 alkenyl group Chemical group 0.000 description 1
- GZVHQXIWLZWABZ-QQTPKPIZSA-N CC(C(N1)=O)=C(/C=C\C=N/C)C1=O Chemical compound CC(C(N1)=O)=C(/C=C\C=N/C)C1=O GZVHQXIWLZWABZ-QQTPKPIZSA-N 0.000 description 1
- SWIQVLDEKWMWAL-UHFFFAOYSA-N CC(C)(C)OC(Cc1cc(O)c(CC(OC(C)(C)C)=O)cc1O)=O Chemical compound CC(C)(C)OC(Cc1cc(O)c(CC(OC(C)(C)C)=O)cc1O)=O SWIQVLDEKWMWAL-UHFFFAOYSA-N 0.000 description 1
- HELJSQCSIVUWCN-UHFFFAOYSA-N CC(CC(C)=C1)C(NC2=O)=C1C2=O Chemical compound CC(CC(C)=C1)C(NC2=O)=C1C2=O HELJSQCSIVUWCN-UHFFFAOYSA-N 0.000 description 1
- NGSJWHJAMHHZIF-UHFFFAOYSA-N COC(Cc(cc(c(CC(O)=O)c1)[O]=C)c1[O]=C)=O Chemical compound COC(Cc(cc(c(CC(O)=O)c1)[O]=C)c1[O]=C)=O NGSJWHJAMHHZIF-UHFFFAOYSA-N 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- 229940126062 Compound A Drugs 0.000 description 1
- 229920000089 Cyclic olefin copolymer Polymers 0.000 description 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- ZDQWESQEGGJUCH-UHFFFAOYSA-N Diisopropyl adipate Chemical compound CC(C)OC(=O)CCCCC(=O)OC(C)C ZDQWESQEGGJUCH-UHFFFAOYSA-N 0.000 description 1
- ORAWFNKFUWGRJG-UHFFFAOYSA-N Docosanamide Chemical compound CCCCCCCCCCCCCCCCCCCCCC(N)=O ORAWFNKFUWGRJG-UHFFFAOYSA-N 0.000 description 1
- OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- KMTRUDSVKNLOMY-UHFFFAOYSA-N Ethylene carbonate Chemical compound O=C1OCCO1 KMTRUDSVKNLOMY-UHFFFAOYSA-N 0.000 description 1
- NLDMNSXOCDLTTB-UHFFFAOYSA-N Heterophylliin A Natural products O1C2COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC2C(OC(=O)C=2C=C(O)C(O)=C(O)C=2)C(O)C1OC(=O)C1=CC(O)=C(O)C(O)=C1 NLDMNSXOCDLTTB-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- IJMWOMHMDSDKGK-UHFFFAOYSA-N Isopropyl propionate Chemical compound CCC(=O)OC(C)C IJMWOMHMDSDKGK-UHFFFAOYSA-N 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 1
- RJUFJBKOKNCXHH-UHFFFAOYSA-N Methyl propionate Chemical compound CCC(=O)OC RJUFJBKOKNCXHH-UHFFFAOYSA-N 0.000 description 1
- FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 description 1
- AMQJEAYHLZJPGS-UHFFFAOYSA-N N-Pentanol Chemical compound CCCCCO AMQJEAYHLZJPGS-UHFFFAOYSA-N 0.000 description 1
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 description 1
- OHLUUHNLEMFGTQ-UHFFFAOYSA-N N-methylacetamide Chemical compound CNC(C)=O OHLUUHNLEMFGTQ-UHFFFAOYSA-N 0.000 description 1
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
- CQYVZXUUXPGQEI-UHFFFAOYSA-N O=C(Cc1c2)Oc1cc(C1)c2OC1=O Chemical compound O=C(Cc1c2)Oc1cc(C1)c2OC1=O CQYVZXUUXPGQEI-UHFFFAOYSA-N 0.000 description 1
- 229920001237 Oxo Biodegradable Polymers 0.000 description 1
- ALQSHHUCVQOPAS-UHFFFAOYSA-N Pentane-1,5-diol Chemical compound OCCCCCO ALQSHHUCVQOPAS-UHFFFAOYSA-N 0.000 description 1
- PWATWSYOIIXYMA-UHFFFAOYSA-N Pentylbenzene Chemical compound CCCCCC1=CC=CC=C1 PWATWSYOIIXYMA-UHFFFAOYSA-N 0.000 description 1
- 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 description 1
- YGYAWVDWMABLBF-UHFFFAOYSA-N Phosgene Chemical compound ClC(Cl)=O YGYAWVDWMABLBF-UHFFFAOYSA-N 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 229920002367 Polyisobutene Polymers 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
- 229920000297 Rayon Polymers 0.000 description 1
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 1
- BOTDANWDWHJENH-UHFFFAOYSA-N Tetraethyl orthosilicate Chemical compound CCO[Si](OCC)(OCC)OCC BOTDANWDWHJENH-UHFFFAOYSA-N 0.000 description 1
- UWHCKJMYHZGTIT-UHFFFAOYSA-N Tetraethylene glycol, Natural products OCCOCCOCCOCCO UWHCKJMYHZGTIT-UHFFFAOYSA-N 0.000 description 1
- YTPLMLYBLZKORZ-UHFFFAOYSA-N Thiophene Chemical group C=1C=CSC=1 YTPLMLYBLZKORZ-UHFFFAOYSA-N 0.000 description 1
- XSTXAVWGXDQKEL-UHFFFAOYSA-N Trichloroethylene Chemical group ClC=C(Cl)Cl XSTXAVWGXDQKEL-UHFFFAOYSA-N 0.000 description 1
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical class CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 1
- RHQDFWAXVIIEBN-UHFFFAOYSA-N Trifluoroethanol Chemical compound OCC(F)(F)F RHQDFWAXVIIEBN-UHFFFAOYSA-N 0.000 description 1
- 239000012963 UV stabilizer Substances 0.000 description 1
- 229920001807 Urea-formaldehyde Polymers 0.000 description 1
- 239000004708 Very-low-density polyethylene Substances 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- 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 description 1
- KXKVLQRXCPHEJC-UHFFFAOYSA-N acetic acid trimethyl ester Natural products COC(C)=O KXKVLQRXCPHEJC-UHFFFAOYSA-N 0.000 description 1
- 125000003670 adamantan-2-yl group Chemical group [H]C1([H])C(C2([H])[H])([H])C([H])([H])C3([H])C([*])([H])C1([H])C([H])([H])C2([H])C3([H])[H] 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 239000002671 adjuvant Substances 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000008044 alkali metal hydroxides Chemical class 0.000 description 1
- 229910000272 alkali metal oxide Inorganic materials 0.000 description 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 1
- 229910000287 alkaline earth metal oxide Inorganic materials 0.000 description 1
- 125000000033 alkoxyamino group Chemical group 0.000 description 1
- OBETXYAYXDNJHR-UHFFFAOYSA-N alpha-ethylcaproic acid Natural products CCCCC(CC)C(O)=O OBETXYAYXDNJHR-UHFFFAOYSA-N 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- CEGOLXSVJUTHNZ-UHFFFAOYSA-K aluminium tristearate Chemical compound [Al+3].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CEGOLXSVJUTHNZ-UHFFFAOYSA-K 0.000 description 1
- 229940063655 aluminum stearate Drugs 0.000 description 1
- BBMXVTPBLPQMAE-UHFFFAOYSA-K aluminum;docosanoate Chemical compound [Al+3].CCCCCCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCCCCCC([O-])=O BBMXVTPBLPQMAE-UHFFFAOYSA-K 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 229920003180 amino resin Polymers 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 238000005280 amorphization Methods 0.000 description 1
- 125000002178 anthracenyl group Chemical group C1(=CC=CC2=CC3=CC=CC=C3C=C12)* 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 239000012431 aqueous reaction media Substances 0.000 description 1
- 239000003125 aqueous solvent Substances 0.000 description 1
- 125000001204 arachidyl 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])C([H])([H])C([H])([H])[H] 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 125000004069 aziridinyl group Chemical group 0.000 description 1
- 239000011324 bead Substances 0.000 description 1
- 125000002511 behenyl 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])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- XVAMCHGMPYWHNL-UHFFFAOYSA-N bemotrizinol Chemical compound OC1=CC(OCC(CC)CCCC)=CC=C1C1=NC(C=2C=CC(OC)=CC=2)=NC(C=2C(=CC(OCC(CC)CCCC)=CC=2)O)=N1 XVAMCHGMPYWHNL-UHFFFAOYSA-N 0.000 description 1
- RNSPZTMNEWTGLN-UHFFFAOYSA-N benzonitrile;pentane Chemical compound CCCCC.N#CC1=CC=CC=C1 RNSPZTMNEWTGLN-UHFFFAOYSA-N 0.000 description 1
- VEKDSSULFPMBDO-UHFFFAOYSA-N benzyl(tritert-butyl)azanium Chemical class CC(C)(C)[N+](C(C)(C)C)(C(C)(C)C)CC1=CC=CC=C1 VEKDSSULFPMBDO-UHFFFAOYSA-N 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 238000006065 biodegradation reaction Methods 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- CMXLJKWFEJEFJE-UHFFFAOYSA-N bis(1,2,2,6,6-pentamethylpiperidin-4-yl) 2-[(4-methoxyphenyl)methylidene]propanedioate Chemical compound C1=CC(OC)=CC=C1C=C(C(=O)OC1CC(C)(C)N(C)C(C)(C)C1)C(=O)OC1CC(C)(C)N(C)C(C)(C)C1 CMXLJKWFEJEFJE-UHFFFAOYSA-N 0.000 description 1
- RSOILICUEWXSLA-UHFFFAOYSA-N bis(1,2,2,6,6-pentamethylpiperidin-4-yl) decanedioate Chemical compound C1C(C)(C)N(C)C(C)(C)CC1OC(=O)CCCCCCCCC(=O)OC1CC(C)(C)N(C)C(C)(C)C1 RSOILICUEWXSLA-UHFFFAOYSA-N 0.000 description 1
- VKVSLLBZHYUYHH-UHFFFAOYSA-N bis(2,2,6,6-tetramethyl-1-octoxypiperidin-3-yl) butanedioate Chemical compound CC1(C)N(OCCCCCCCC)C(C)(C)CCC1OC(=O)CCC(=O)OC1C(C)(C)N(OCCCCCCCC)C(C)(C)CC1 VKVSLLBZHYUYHH-UHFFFAOYSA-N 0.000 description 1
- 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 description 1
- 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 description 1
- GOJOVSYIGHASEI-UHFFFAOYSA-N bis(2,2,6,6-tetramethylpiperidin-4-yl) butanedioate Chemical compound C1C(C)(C)NC(C)(C)CC1OC(=O)CCC(=O)OC1CC(C)(C)NC(C)(C)C1 GOJOVSYIGHASEI-UHFFFAOYSA-N 0.000 description 1
- XITRBUPOXXBIJN-UHFFFAOYSA-N bis(2,2,6,6-tetramethylpiperidin-4-yl) decanedioate Chemical compound C1C(C)(C)NC(C)(C)CC1OC(=O)CCCCCCCCC(=O)OC1CC(C)(C)NC(C)(C)C1 XITRBUPOXXBIJN-UHFFFAOYSA-N 0.000 description 1
- FQUNFJULCYSSOP-UHFFFAOYSA-N bisoctrizole Chemical compound N1=C2C=CC=CC2=NN1C1=CC(C(C)(C)CC(C)(C)C)=CC(CC=2C(=C(C=C(C=2)C(C)(C)CC(C)(C)C)N2N=C3C=CC=CC3=N2)O)=C1O FQUNFJULCYSSOP-UHFFFAOYSA-N 0.000 description 1
- 230000000740 bleeding effect Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- 230000001680 brushing effect Effects 0.000 description 1
- KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 description 1
- 229940043232 butyl acetate Drugs 0.000 description 1
- 125000006309 butyl amino group Chemical group 0.000 description 1
- 125000006487 butyl benzyl group Chemical group 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- QHIWVLPBUQWDMQ-UHFFFAOYSA-N butyl prop-2-enoate;methyl 2-methylprop-2-enoate;prop-2-enoic acid Chemical compound OC(=O)C=C.COC(=O)C(C)=C.CCCCOC(=O)C=C QHIWVLPBUQWDMQ-UHFFFAOYSA-N 0.000 description 1
- 238000003490 calendering Methods 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 150000001244 carboxylic acid anhydrides Chemical class 0.000 description 1
- 239000005018 casein Substances 0.000 description 1
- BECPQYXYKAMYBN-UHFFFAOYSA-N casein, tech. Chemical compound NCCCCC(C(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(CC(C)C)N=C(O)C(CCC(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(C(C)O)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(COP(O)(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(N)CC1=CC=CC=C1 BECPQYXYKAMYBN-UHFFFAOYSA-N 0.000 description 1
- 235000021240 caseins Nutrition 0.000 description 1
- 238000005266 casting Methods 0.000 description 1
- 229920002301 cellulose acetate Polymers 0.000 description 1
- 229920003086 cellulose ether Polymers 0.000 description 1
- 238000005119 centrifugation Methods 0.000 description 1
- 239000007809 chemical reaction catalyst Substances 0.000 description 1
- XTHPWXDJESJLNJ-UHFFFAOYSA-N chlorosulfonic acid Substances OS(Cl)(=O)=O XTHPWXDJESJLNJ-UHFFFAOYSA-N 0.000 description 1
- 238000004737 colorimetric analysis Methods 0.000 description 1
- 239000006103 coloring component Substances 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 238000000748 compression moulding Methods 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- MGNCLNQXLYJVJD-UHFFFAOYSA-N cyanuric chloride Chemical compound ClC1=NC(Cl)=NC(Cl)=N1 MGNCLNQXLYJVJD-UHFFFAOYSA-N 0.000 description 1
- 125000000000 cycloalkoxy group Chemical group 0.000 description 1
- 125000001995 cyclobutyl group Chemical group [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
- 125000000582 cycloheptyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
- 125000004210 cyclohexylmethyl group Chemical group [H]C([H])(*)C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C1([H])[H] 0.000 description 1
- 125000000640 cyclooctyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C([H])([H])C1([H])[H] 0.000 description 1
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 description 1
- 125000004186 cyclopropylmethyl group Chemical group [H]C([H])(*)C1([H])C([H])([H])C1([H])[H] 0.000 description 1
- 230000006378 damage Effects 0.000 description 1
- 125000003493 decenyl group Chemical group [H]C([*])=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])[H] 0.000 description 1
- 125000002704 decyl 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])* 0.000 description 1
- 239000002274 desiccant Substances 0.000 description 1
- JQVDAXLFBXTEQA-UHFFFAOYSA-N dibutylamine Chemical compound CCCCNCCCC JQVDAXLFBXTEQA-UHFFFAOYSA-N 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 229940028356 diethylene glycol monobutyl ether Drugs 0.000 description 1
- XXJWXESWEXIICW-UHFFFAOYSA-N diethylene glycol monoethyl ether Chemical compound CCOCCOCCO XXJWXESWEXIICW-UHFFFAOYSA-N 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- SZXQTJUDPRGNJN-UHFFFAOYSA-N dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 description 1
- 229940113120 dipropylene glycol Drugs 0.000 description 1
- KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical class [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- ZITKDVFRMRXIJQ-UHFFFAOYSA-N dodecane-1,2-diol Chemical compound CCCCCCCCCCC(O)CO ZITKDVFRMRXIJQ-UHFFFAOYSA-N 0.000 description 1
- 125000005066 dodecenyl group Chemical group C(=CCCCCCCCCCC)* 0.000 description 1
- ODQWQRRAPPTVAG-GZTJUZNOSA-N doxepin Chemical compound C1OC2=CC=CC=C2C(=C/CCN(C)C)/C2=CC=CC=C21 ODQWQRRAPPTVAG-GZTJUZNOSA-N 0.000 description 1
- MCPKSFINULVDNX-UHFFFAOYSA-N drometrizole Chemical compound CC1=CC=C(O)C(N2N=C3C=CC=CC3=N2)=C1 MCPKSFINULVDNX-UHFFFAOYSA-N 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 239000012636 effector Substances 0.000 description 1
- 230000032050 esterification Effects 0.000 description 1
- 238000005886 esterification reaction Methods 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 239000007888 film coating Substances 0.000 description 1
- 238000009501 film coating Methods 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000010419 fine particle Substances 0.000 description 1
- 235000019253 formic acid Nutrition 0.000 description 1
- 238000007710 freezing Methods 0.000 description 1
- 230000008014 freezing Effects 0.000 description 1
- 238000007429 general method Methods 0.000 description 1
- 239000003365 glass fiber Substances 0.000 description 1
- 239000003966 growth inhibitor Substances 0.000 description 1
- 150000008282 halocarbons Chemical class 0.000 description 1
- 229910001385 heavy metal Inorganic materials 0.000 description 1
- 125000000755 henicosyl 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])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000003187 heptyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 description 1
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 1
- 125000006038 hexenyl group Chemical group 0.000 description 1
- 229940051250 hexylene glycol Drugs 0.000 description 1
- 229920001903 high density polyethylene Polymers 0.000 description 1
- 239000004700 high-density polyethylene Substances 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 125000002636 imidazolinyl group Chemical group 0.000 description 1
- 125000002883 imidazolyl group Chemical group 0.000 description 1
- 238000002329 infrared spectrum Methods 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 238000001746 injection moulding Methods 0.000 description 1
- 239000012784 inorganic fiber Substances 0.000 description 1
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 description 1
- WDAXFOBOLVPGLV-UHFFFAOYSA-N isobutyric acid ethyl ester Natural products CCOC(=O)C(C)C WDAXFOBOLVPGLV-UHFFFAOYSA-N 0.000 description 1
- JMMWKPVZQRWMSS-UHFFFAOYSA-N isopropanol acetate Natural products CC(C)OC(C)=O JMMWKPVZQRWMSS-UHFFFAOYSA-N 0.000 description 1
- 229940011051 isopropyl acetate Drugs 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 125000001786 isothiazolyl group Chemical group 0.000 description 1
- GWYFCOCPABKNJV-UHFFFAOYSA-N isovaleric acid Chemical compound CC(C)CC(O)=O GWYFCOCPABKNJV-UHFFFAOYSA-N 0.000 description 1
- 239000004310 lactic acid Substances 0.000 description 1
- 235000014655 lactic acid Nutrition 0.000 description 1
- 238000004989 laser desorption mass spectroscopy Methods 0.000 description 1
- 125000002463 lignoceryl 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])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000000944 linseed oil Substances 0.000 description 1
- 235000021388 linseed oil Nutrition 0.000 description 1
- 229920001684 low density polyethylene Polymers 0.000 description 1
- 239000004702 low-density polyethylene Substances 0.000 description 1
- 235000019359 magnesium stearate Nutrition 0.000 description 1
- OBQVOBQZMOXRAL-UHFFFAOYSA-L magnesium;docosanoate Chemical compound [Mg+2].CCCCCCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCCCCCC([O-])=O OBQVOBQZMOXRAL-UHFFFAOYSA-L 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 125000002960 margaryl 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])[H] 0.000 description 1
- 238000004949 mass spectrometry Methods 0.000 description 1
- 238000000691 measurement method Methods 0.000 description 1
- 150000007974 melamines Chemical class 0.000 description 1
- 150000002734 metacrylic acid derivatives Chemical class 0.000 description 1
- UZKWTJUDCOPSNM-UHFFFAOYSA-N methoxybenzene Substances CCCCOC=C UZKWTJUDCOPSNM-UHFFFAOYSA-N 0.000 description 1
- UJRDRFZCRQNLJM-UHFFFAOYSA-N methyl 3-[3-(benzotriazol-2-yl)-5-tert-butyl-4-hydroxyphenyl]propanoate Chemical compound CC(C)(C)C1=CC(CCC(=O)OC)=CC(N2N=C3C=CC=CC3=N2)=C1O UJRDRFZCRQNLJM-UHFFFAOYSA-N 0.000 description 1
- 229940057867 methyl lactate Drugs 0.000 description 1
- 229940017219 methyl propionate Drugs 0.000 description 1
- QLPMKRZYJPNIRP-UHFFFAOYSA-M methyl(trioctyl)azanium;bromide Chemical compound [Br-].CCCCCCCC[N+](C)(CCCCCCCC)CCCCCCCC QLPMKRZYJPNIRP-UHFFFAOYSA-M 0.000 description 1
- GYNNXHKOJHMOHS-UHFFFAOYSA-N methyl-cycloheptane Natural products CC1CCCCCC1 GYNNXHKOJHMOHS-UHFFFAOYSA-N 0.000 description 1
- 239000010445 mica Substances 0.000 description 1
- 229910052618 mica group Inorganic materials 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 125000002950 monocyclic group Chemical group 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 125000002757 morpholinyl group Chemical group 0.000 description 1
- GXFQBBOZTNQHMW-UHFFFAOYSA-N n'-(2,2,6,6-tetramethylpiperidin-4-yl)hexane-1,6-diamine Chemical compound CC1(C)CC(NCCCCCCN)CC(C)(C)N1 GXFQBBOZTNQHMW-UHFFFAOYSA-N 0.000 description 1
- SRLHDBRENZFCIN-UHFFFAOYSA-N n,n-di(butan-2-yl)butan-2-amine Chemical class CCC(C)N(C(C)CC)C(C)CC SRLHDBRENZFCIN-UHFFFAOYSA-N 0.000 description 1
- SYSQUGFVNFXIIT-UHFFFAOYSA-N n-[4-(1,3-benzoxazol-2-yl)phenyl]-4-nitrobenzenesulfonamide Chemical class C1=CC([N+](=O)[O-])=CC=C1S(=O)(=O)NC1=CC=C(C=2OC3=CC=CC=C3N=2)C=C1 SYSQUGFVNFXIIT-UHFFFAOYSA-N 0.000 description 1
- UONLDZHKYCFZRW-UHFFFAOYSA-N n-[6-[formyl-(2,2,6,6-tetramethylpiperidin-4-yl)amino]hexyl]-n-(2,2,6,6-tetramethylpiperidin-4-yl)formamide Chemical compound C1C(C)(C)NC(C)(C)CC1N(C=O)CCCCCCN(C=O)C1CC(C)(C)NC(C)(C)C1 UONLDZHKYCFZRW-UHFFFAOYSA-N 0.000 description 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- DARUEKWVLGHJJT-UHFFFAOYSA-N n-butyl-1-[4-[4-(butylamino)-2,2,6,6-tetramethylpiperidin-1-yl]-6-chloro-1,3,5-triazin-2-yl]-2,2,6,6-tetramethylpiperidin-4-amine Chemical compound CC1(C)CC(NCCCC)CC(C)(C)N1C1=NC(Cl)=NC(N2C(CC(CC2(C)C)NCCCC)(C)C)=N1 DARUEKWVLGHJJT-UHFFFAOYSA-N 0.000 description 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 description 1
- 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 description 1
- GOQYKNQRPGWPLP-UHFFFAOYSA-N n-heptadecyl alcohol Natural products CCCCCCCCCCCCCCCCCO GOQYKNQRPGWPLP-UHFFFAOYSA-N 0.000 description 1
- 125000001624 naphthyl group Chemical group 0.000 description 1
- 239000005445 natural material Substances 0.000 description 1
- 239000000025 natural resin Substances 0.000 description 1
- 229910017604 nitric acid Inorganic materials 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- ODUCDPQEXGNKDN-UHFFFAOYSA-N nitroxyl Chemical group O=N ODUCDPQEXGNKDN-UHFFFAOYSA-N 0.000 description 1
- 125000001196 nonadecyl 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])C([H])([H])[H] 0.000 description 1
- 125000005187 nonenyl group Chemical group C(=CCCCCCCC)* 0.000 description 1
- 125000001400 nonyl 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])[H] 0.000 description 1
- 125000002868 norbornyl group Chemical group C12(CCC(CC1)C2)* 0.000 description 1
- 125000005482 norpinyl group Chemical group 0.000 description 1
- 125000005064 octadecenyl group Chemical group C(=CCCCCCCCCCCCCCCCC)* 0.000 description 1
- SSDSCDGVMJFTEQ-UHFFFAOYSA-N octadecyl 3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)CCC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 SSDSCDGVMJFTEQ-UHFFFAOYSA-N 0.000 description 1
- 125000004365 octenyl group Chemical group C(=CCCCCCC)* 0.000 description 1
- DMFXLIFZVRXRRR-UHFFFAOYSA-N octyl 3-[3-tert-butyl-5-(5-chlorobenzotriazol-2-yl)-4-hydroxyphenyl]propanoate Chemical compound CC(C)(C)C1=CC(CCC(=O)OCCCCCCCC)=CC(N2N=C3C=C(Cl)C=CC3=N2)=C1O DMFXLIFZVRXRRR-UHFFFAOYSA-N 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 235000019198 oils Nutrition 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 238000000399 optical microscopy Methods 0.000 description 1
- 239000012074 organic phase Substances 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 125000002971 oxazolyl group Chemical group 0.000 description 1
- 125000003566 oxetanyl group Chemical group 0.000 description 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
- JCGNDDUYTRNOFT-UHFFFAOYSA-N oxolane-2,4-dione Chemical compound O=C1COC(=O)C1 JCGNDDUYTRNOFT-UHFFFAOYSA-N 0.000 description 1
- 125000004430 oxygen atom Chemical group O* 0.000 description 1
- NFHFRUOZVGFOOS-UHFFFAOYSA-N palladium;triphenylphosphane Chemical compound [Pd].C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 NFHFRUOZVGFOOS-UHFFFAOYSA-N 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 229940112041 peripherally acting muscle relaxants other quaternary ammonium compound in atc Drugs 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- 125000005561 phenanthryl group Chemical group 0.000 description 1
- 229920001568 phenolic resin Polymers 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 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 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 239000006069 physical mixture Substances 0.000 description 1
- 239000006187 pill Substances 0.000 description 1
- 125000004193 piperazinyl group Chemical group 0.000 description 1
- XUWHAWMETYGRKB-UHFFFAOYSA-N piperidin-2-one Chemical compound O=C1CCCCN1 XUWHAWMETYGRKB-UHFFFAOYSA-N 0.000 description 1
- 125000003386 piperidinyl group Chemical group 0.000 description 1
- 239000002798 polar solvent Substances 0.000 description 1
- 229920002587 poly(1,3-butadiene) polymer Polymers 0.000 description 1
- 229920000191 poly(N-vinyl pyrrolidone) Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920001707 polybutylene terephthalate Polymers 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229940113115 polyethylene glycol 200 Drugs 0.000 description 1
- 229940068918 polyethylene glycol 400 Drugs 0.000 description 1
- 229940057847 polyethylene glycol 600 Drugs 0.000 description 1
- 229920000139 polyethylene terephthalate Polymers 0.000 description 1
- 239000005020 polyethylene terephthalate Substances 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 1
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- 229940064298 pregnyl Drugs 0.000 description 1
- 230000003449 preventive effect Effects 0.000 description 1
- 150000003141 primary amines Chemical class 0.000 description 1
- 239000011164 primary particle Substances 0.000 description 1
- 235000019260 propionic acid Nutrition 0.000 description 1
- MCSINKKTEDDPNK-UHFFFAOYSA-N propyl propionate Chemical compound CCCOC(=O)CC MCSINKKTEDDPNK-UHFFFAOYSA-N 0.000 description 1
- 125000003072 pyrazolidinyl group Chemical group 0.000 description 1
- 125000002755 pyrazolinyl group Chemical group 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 125000000719 pyrrolidinyl group Chemical group 0.000 description 1
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 238000002310 reflectometry Methods 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 238000000790 scattering method Methods 0.000 description 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- ZJMWRROPUADPEA-UHFFFAOYSA-N sec-butylbenzene Chemical compound CCC(C)C1=CC=CC=C1 ZJMWRROPUADPEA-UHFFFAOYSA-N 0.000 description 1
- 125000000467 secondary amino group Chemical group [H]N([*:1])[*:2] 0.000 description 1
- 238000007493 shaping process Methods 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- VARHTEOJTOSPMY-UHFFFAOYSA-M sodium;2,3-dioxo-1h-indole-5-sulfonate Chemical compound [Na+].[O-]S(=O)(=O)C1=CC=C2NC(=O)C(=O)C2=C1 VARHTEOJTOSPMY-UHFFFAOYSA-M 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 239000011877 solvent mixture Substances 0.000 description 1
- 238000004611 spectroscopical analysis Methods 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 238000013112 stability test Methods 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 229940037312 stearamide Drugs 0.000 description 1
- 229960004274 stearic acid Drugs 0.000 description 1
- 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 description 1
- 238000007155 step growth polymerization reaction Methods 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- HXJUTPCZVOIRIF-UHFFFAOYSA-N sulfolane Chemical compound O=S1(=O)CCCC1 HXJUTPCZVOIRIF-UHFFFAOYSA-N 0.000 description 1
- HIFJUMGIHIZEPX-UHFFFAOYSA-N sulfuric acid;sulfur trioxide Chemical compound O=S(=O)=O.OS(O)(=O)=O HIFJUMGIHIZEPX-UHFFFAOYSA-N 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 229920005613 synthetic organic polymer Polymers 0.000 description 1
- 238000010345 tape casting Methods 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 125000005063 tetradecenyl group Chemical group C(=CCCCCCCCCCCCC)* 0.000 description 1
- HWCKGOZZJDHMNC-UHFFFAOYSA-M tetraethylammonium bromide Chemical compound [Br-].CC[N+](CC)(CC)CC HWCKGOZZJDHMNC-UHFFFAOYSA-M 0.000 description 1
- 125000003831 tetrazolyl group Chemical group 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 229920005992 thermoplastic resin Polymers 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
- VLLMWSRANPNYQX-UHFFFAOYSA-N thiadiazole Chemical compound C1=CSN=N1.C1=CSN=N1 VLLMWSRANPNYQX-UHFFFAOYSA-N 0.000 description 1
- YODZTKMDCQEPHD-UHFFFAOYSA-N thiodiglycol Chemical compound OCCSCCO YODZTKMDCQEPHD-UHFFFAOYSA-N 0.000 description 1
- 229950006389 thiodiglycol Drugs 0.000 description 1
- 230000009974 thixotropic effect Effects 0.000 description 1
- 235000010215 titanium dioxide Nutrition 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- 238000005809 transesterification reaction Methods 0.000 description 1
- 125000004306 triazinyl group Chemical group 0.000 description 1
- 150000003852 triazoles Chemical class 0.000 description 1
- 125000002889 tridecyl 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])[H] 0.000 description 1
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1
- JLGLQAWTXXGVEM-UHFFFAOYSA-N triethylene glycol monomethyl ether Chemical compound COCCOCCOCCO JLGLQAWTXXGVEM-UHFFFAOYSA-N 0.000 description 1
- RKBCYCFRFCNLTO-UHFFFAOYSA-N triisopropylamine Chemical class CC(C)N(C(C)C)C(C)C RKBCYCFRFCNLTO-UHFFFAOYSA-N 0.000 description 1
- SZEMGTQCPRNXEG-UHFFFAOYSA-M trimethyl(octadecyl)azanium;bromide Chemical compound [Br-].CCCCCCCCCCCCCCCCCC[N+](C)(C)C SZEMGTQCPRNXEG-UHFFFAOYSA-M 0.000 description 1
- GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical class CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 description 1
- YFTHZRPMJXBUME-UHFFFAOYSA-N tripropylamine Chemical class CCCN(CCC)CCC YFTHZRPMJXBUME-UHFFFAOYSA-N 0.000 description 1
- 229920000785 ultra high molecular weight polyethylene Polymers 0.000 description 1
- 229920001862 ultra low molecular weight polyethylene Polymers 0.000 description 1
- 238000002604 ultrasonography Methods 0.000 description 1
- 125000002948 undecyl 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])[H] 0.000 description 1
- 239000003981 vehicle Substances 0.000 description 1
- PXXNTAGJWPJAGM-UHFFFAOYSA-N vertaline Natural products C1C2C=3C=C(OC)C(OC)=CC=3OC(C=C3)=CC=C3CCC(=O)OC1CC1N2CCCC1 PXXNTAGJWPJAGM-UHFFFAOYSA-N 0.000 description 1
- 229920001866 very low density polyethylene Polymers 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 238000001238 wet grinding Methods 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
- 229910052724 xenon Inorganic materials 0.000 description 1
- FHNFHKCVQCLJFQ-UHFFFAOYSA-N xenon atom Chemical compound [Xe] FHNFHKCVQCLJFQ-UHFFFAOYSA-N 0.000 description 1
- 238000004383 yellowing Methods 0.000 description 1
- XOOUIPVCVHRTMJ-UHFFFAOYSA-L zinc stearate Chemical compound [Zn+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O XOOUIPVCVHRTMJ-UHFFFAOYSA-L 0.000 description 1
- IJQXGKBNDNQWAT-UHFFFAOYSA-L zinc;docosanoate Chemical compound [Zn+2].CCCCCCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCCCCCC([O-])=O IJQXGKBNDNQWAT-UHFFFAOYSA-L 0.000 description 1
- 239000004711 α-olefin Substances 0.000 description 1
- PAPBSGBWRJIAAV-UHFFFAOYSA-N ε-Caprolactone Chemical compound O=C1CCCCCO1 PAPBSGBWRJIAAV-UHFFFAOYSA-N 0.000 description 1
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B57/00—Other synthetic dyes of known constitution
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
- A01N43/74—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,3
- A01N43/78—1,3-Thiazoles; Hydrogenated 1,3-thiazoles
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/04—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D493/00—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system
- C07D493/02—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system in which the condensed system contains two hetero rings
- C07D493/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/16—Nitrogen-containing compounds
- C08K5/34—Heterocyclic compounds having nitrogen in the ring
- C08K5/3412—Heterocyclic compounds having nitrogen in the ring having one nitrogen atom in the ring
- C08K5/3415—Five-membered rings
- C08K5/3417—Five-membered rings condensed with carbocyclic rings
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B67/00—Influencing the physical, e.g. the dyeing or printing properties of dyestuffs without chemical reactions, e.g. by treating with solvents grinding or grinding assistants, coating of pigments or dyes; Process features in the making of dyestuff preparations; Dyestuff preparations of a special physical nature, e.g. tablets, films
- C09B67/0033—Blends of pigments; Mixtured crystals; Solid solutions
- C09B67/0034—Mixtures of two or more pigments or dyes of the same type
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/0008—Organic ingredients according to more than one of the "one dot" groups of C08K5/01 - C08K5/59
- C08K5/0041—Optical brightening agents, organic pigments
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
- Y10T428/2982—Particulate matter [e.g., sphere, flake, etc.]
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T442/00—Fabric [woven, knitted, or nonwoven textile or cloth, etc.]
- Y10T442/30—Woven fabric [i.e., woven strand or strip material]
Abstract
Description
上記式中、
R1およびR2は、互いに独立にHであるかまたはそれぞれ置換されていないかまたはハロゲンまたはC1〜C8アルコキシによって置換された、C1〜C24アルキル、C3〜C24シクロアルキル、C2〜C24アルケニル、C3〜C24シクロアルケニルまたはC2〜C24アルキニルであり;置換されていないかまたは1回または数回ハロゲン、ニトロ、シアノ、C1〜C8アルキルおよび/またはC1〜C8アルコキシによって置換されたC7〜C24アラルキルであり;または置換されていないかまたは1回または数回ハロゲン、ニトロ、シアノ、C1〜C8アルキルおよび/またはC1〜C8アルコキシによって置換されたC6〜C24アリールであり;
R3は、H、F、Cl、R8またはOR8、好ましくはHまたはFであり;
R4、R5およびR6は、互いに独立にH、F、Br、Cl、COOH、COOR8、CONH2、CONHR8、CONR8R8、CN、COR8、SO3H、SO2Cl、SO2NH2、SO2NHR8、SO2NR8R8、SO2R8、NO2、R8、OR8、SR8、NR8R8、NHCOR8または
R7は、Hであるかまたはそれぞれ置換されていないかまたは1回または数回F、オキソまたはチオキソによって置換され、および中断されていないかまたは1回または数回O、SまたはNR8によって中断された、C1〜C24アルキル、C3〜C24シクロアルキル、C2〜C24アルケニル、C3〜C24シクロアルケニル、C2〜C24アルキニルまたはC2〜C12ヘテロシクロアルキルであり;またはそれぞれ置換されていないかまたは1回または数回オキソ、チオキソ、F、Br、Cl、COOH、COOR8、CONH2、CONHR8、CONR8R8、CN、COR8、SO3H、SO3Cl、SO2NH2、SO2NHR8、SO2NR8R8、SO2R8、NO2、R8、OR8、SR8、NR8R8、NHCOR8または
それぞれR8は、全ての他のR8とは独立に、それぞれ置換されていないかまたは1回または数回F、オキソ、チオキソ、OR9、SR9またはNR9R9によって置換された、C1〜C24アルキル、C3〜C24シクロアルキル、C2〜C24アルケニル、C3〜C24シクロアルケニル、C2〜C24アルキニルまたはC2〜C12ヘテロシクロアルキルであり;またはそれぞれ置換されていないかまたは1回または数回オキソ、F、Br、Cl、COOH、CONH2、CONHR9、CONR9R9、SO3H、SO2Cl、SO2NH2、SO2NHR9、SO2NHR9R9、CN、NO2、OR9、SR9、NR9R9、NHCOR9または
2個のビシナルR8は、一緒になって−O−CO−O−、−O−CS−O−、−CO−N−CO−、−N−CO−N−、−N=S=N−、−N−C=C−、−O−C=C−、−S−C=C−、−O−C=N−、−S−C=N−、−N−N=N−、−N=C−C=C−、−C=N−C=C−、−N=C−C=N−、−C=N−N=C−または−C=N−C=N−または−C=C−C=C−を形成し、この場合それぞれ−C=および−N−は、全ての他の−C=および−N−とは独立にHまたはR9によって置換されており;または
2個のジェミナルまたはビシナルR8は、一緒になって、それぞれ置換されていないかまたは1回または数回F、オキソまたはチオキソによって置換された、C3〜C8アルキレンまたはC3〜C8アルケニレン基を形成し、この場合0、1または2個のノンビシナルメチレン単位は、O、SまたはNR9によって置換されていてよく;および
それぞれR9は、全ての他のR9とは独立に、それぞれ置換されていないかまたは1回または数回オキソ、チオキソ、Fおよび/またはO−C1〜C8アルキルによって置換された、C1〜C8アルキル、C3〜C6シクロアルキルまたはベンジルであり;またはそれぞれ置換されていないかまたは1回または数回F、Br、Cl、CO−C1〜C8アルキル、COOH、CONH、CONHC1〜C8アルキル、CON(C1〜C8アルキル)2、SO3H、SO3Cl、SO2NH2、SO2NHC1〜C8アルキル、SO2N(C1〜C8アルキル)2、CN、NO2、C1〜C8アルキル、OC1〜C8アルキル、SC1〜C8アルキルまたはN(C1〜C8アルキル)によって置換された、フェニルまたはC1〜C5ヘテロアリールであり;または
2個のビシナルR9は、一緒になって−O−CO−O−、−O−CS−O−、−CO−N−CO−、−N−CO−N−、−N=S=N−、−N−C=C−、−O−C=C−、−S−C=C−、−O−C=N−、−S−C=N−、−N−N=N−、−N=C−C=C−、−C=N−C=C−、−N=C−C=N−、−C=N−N=C−または−C=N−C=N−または−C=C−C=C−を形成し、この場合それぞれ−C=および−N−は、全ての他の−C=および−N−とは独立にH、F、オキソ、チオキソ、C1〜C8アルキルまたはOC1〜C8アルキルによって置換されており;または
2個のジェミナルまたはビシナルR9は、一緒になって、それぞれ置換されていないかまたは1回または数回オキソまたはチオキソによって置換された、C3〜C8アルキレンまたはC3〜C8アルケニレン基を形成し、この場合0、1または2個のノンビシナルメチレン単位は、O、SまたはN(C1〜C8アルキル)によって置換されていてよい。
R3=R4=R5=R6=R7=H;
R3=R5=R6=R7=H、R4=NO2;
R3=R5=R6=R7=H、R4=OCH3;
R3=R5=R6=R7=H、R4=Cl;
R3=R5=R6=R7=H、R4=F;
R3=R5=R6=R7=H、R4=Br;
R3=R5=R6=R7=H、R4=SO3H;
R3=R5=R6=R7=H、R4=COOH;
R3=R5=R6=R7=H、R4=N(CH3)2;
R3=R5=R6=R7=H、R4=NHCOC1〜C18アルキル、特にNHCOC1〜C12アルキル;
R3=R5=R6=R7=H、R4=C1〜C20アルキル、特にC1〜C14アルキル;
R3=R5=R6=R7=H、R4=C2〜C20アルコキシ、特にC2〜C14アルコキシ;
R3=R5=R7=H、R4=R6=CH3;
R3=R5=R7=H、R4=R6=Cl;
R3=R5=R7=H、R4=Cl、R6=CH3;
R3=R4=R5=R6=H、R7=CH3;
R3=R4=R5=R6=H、R7=C6H5;および
R3=R4=R7=H、R5およびR6が一緒になって=1,4−ブタジエニレン。
T=遠心分離時間 分;
d=粒径 μm;
N=毎分の回転数(=10000);
p=粒子充填量と初期流体充填量との密度差、mg/cm3;
η=流体の粘度 ポアズ;
R’’=ディスクの周辺測定位置での半径、cm;
R’=ディスクの中心付近での噴射位置での半径、cm〕を用いて測定される。
7.8s、10.2w、12.6s、18.6w、21.8w、22.4w、24.4m、25.0w、26.7m、27.2mおよび28.8w °2Θで線を有するX線粉末回折図(図1)によって特徴付けられた、実験式C26H12N2O6のモル比1:2での
R10は、H、CH3、C2H5、OCH3、OC2H5、F、Cl、Br、NO2、CN、COOHまたはSO3Hであり、
R11は、H、NO2、CN、COOHまたはSO3Hであり、および
R12は、H、CH3、C2H5、OCH3、OC2H5、FまたはClである〕で示される2〜5つの化合物と1:2の全体のモル比(i):(iv)で、水中で25℃で4.5以下のpKを有する触媒の存在下で反応させることによって特徴付けられた、黒色着色剤を製造する方法も提供する。
R13は、H、C1〜C8アルキル、OC1〜C8アルコキシ、F、Cl、Br、NO2、CN、COOHまたはSO3Hであり、
R14は、H、NO2、CN、COOHまたはSO3Hであり、およびR15は、H、ClまたはC1〜C8アルキルである。
7.6s、9.5w、11.8s、20.7w、24.7m、26.4mおよび28.4m °2Θで線を有するX線粉末回折図(図25)によって特徴付けられた、実験式C26H12N2O6、C28H16N2O6およびC30H20N2O6の化合物を有する、モル比1:1:1での
理論値:C 67.92 H 8.85 N 4.17 O 14.29 S 4.77;
実測値:C 66.35 H 9.11 N 3.77 O 14.30 S 5.45。
理論値:C 61.35 H 6.24 N 4.57 O 20.87 S 6.97;
実測値:C 58.90 H 7.47 N 4.01 O 21.25 S 6.74。
Claims (18)
- 黒色着色剤、好ましくは黒色顔料を製造する方法において、式
上記式中、
R1およびR2は、互いに独立にHであるかまたはそれぞれ置換されていないかまたはハロゲンまたはC1〜C8アルコキシによって置換された、C1〜C24アルキル、C3〜C24シクロアルキル、C2〜C24アルケニル、C3〜C24シクロアルケニルまたはC2〜C24アルキニルであり;置換されていないかまたは1回または数回ハロゲン、ニトロ、シアノ、C1〜C8アルキルおよび/またはC1〜C8アルコキシによって置換されたC7〜C24アラルキルであり;または置換されていないかまたは1回または数回ハロゲン、ニトロ、シアノ、C1〜C8アルキルおよび/またはC1〜C8アルコキシによって置換されたC6〜C24アリールであり;
R3は、H、F、Cl、R8またはOR8、好ましくはHまたはFであり;
R4、R5およびR6は、互いに独立にH、F、Br、Cl、COOH、COOR8、CONH2、CONHR8、CONR8R8、CN、COR8、SO3H、SO2Cl、SO2NH2、SO2NHR8、SO2NR8R8、SO2R8、NO2であり、
R8は、OR8、SR8、NR8R8、NHCOR8または
R3とR4、R4とR5またはR5とR6は、一緒になって対で、それぞれ置換されていないかまたは1回または数回F、OR、NO、オキソ、チキソまたはSOHによって置換されたC1〜C8アルケンジオキシ基、C3〜C6アルキレン基、C3〜C6アルケニレン基または1,4−ブタジエニレン基を形成し;
R7は、Hであるかまたはそれぞれ置換されていないかまたは1回または数回F、オキソまたはチオキソによって置換され、および中断されていないかまたは1回または数回O、SまたはNR8によって中断された、C1〜C24アルキル、C3〜C24シクロアルキル、C2〜C24アルケニル、C3〜C24シクロアルケニル、C2〜C24アルキニルまたはC2〜C12ヘテロシクロアルキルであり;またはそれぞれ置換されていないかまたは1回または数回オキソ、チオキソ、F、Br、Cl、COOH、COOR8、CONH2、CONHR8、CONR8R8、CN、COR8、SO3H、SO3Cl、SO2NH2、SO2NHR8、SO2NR8R8、SO2R8、NO2、R8、OR8、SR8、NR8R8、NHCOR8または
それぞれR8は、全ての他のR8とは独立に、それぞれ置換されていないかまたは1回または数回F、オキソ、チオキソ、OR9、SR9またはNR9R9によって置換された、C1〜C24アルキル、C3〜C24シクロアルキル、C2〜C24アルケニル、C3〜C24シクロアルケニル、C2〜C24アルキニルまたはC2〜C12ヘテロシクロアルキルであり;またはそれぞれ置換されていないかまたは1回または数回オキソ、F、Br、Cl、COOH、CONH2、CONHR9、CONR9R9、SO3H、SO2Cl、SO2NH2、SO2NHR9、SO2NHR9R9、CN、NO2、OR9、SR9、NR9R9、NHCOR9または
または2個のビシナル−R8は、一緒になって−O−CO−O−、−O−CS−O−、−CO−N−CO−、−N−CO−N−、−N=S=N−、−N−C=C−、−O−C=C−、−S−C=C−、−O−C=N−、−S−C=N−、−N−N=N−、−N=C−C=C−、−C=N−C=C−、−N=C−C=N−、−C=N−N=C−または−C=N−C=N−または−C=C−C=C−を形成し、この場合それぞれ−C=および−N−は、全ての他の−C=および−N−とは独立にHまたはR9によって置換されており;
または2個のジェミナルまたはビシナルR8は、一緒になって、それぞれ置換されていないかまたは1回または数回F、オキソまたはチオキソによって置換された、C3〜C8アルキレンまたはC3〜C8アルケニレン基を形成し、この場合0、1または2個のノンビシナルメチレン単位は、O、SまたはNR9によって置換されていてよく;および
それぞれR9は、全ての他のR9とは独立に、それぞれ置換されていないかまたは1回または数回オキソ、チオキソ、Fおよび/またはO−C1〜C8アルキルによって置換された、C1〜C8アルキル、C3〜C6シクロアルキルまたはベンジルであり;またはそれぞれ置換されていないかまたは1回または数回F、Br、Cl、CO−C1〜C8アルキル、COOH、CONH、CONHC1〜C8アルキル、CON(C1〜C8アルキル)2、SO3H、SO3Cl、SO2NH2、SO2NHC1〜C8アルキル、SO2N(C1〜C8アルキル)2、CN、NO2、C1〜C8アルキル、OC1〜C8アルキル、SC1〜C8アルキルまたはN(C1〜C8アルキル)によって置換された、フェニルまたはC1〜C5ヘテロアリールであり;
または2個のビシナルR9は、一緒になって−O−CO−O−、−O−CS−O−、−CO−N−CO−、−N−CO−N−、−N=S=N−、−N−C=C−、−O−C=C−、−S−C=C−、−O−C=N−、−S−C=N−、−N−N=N−、−N=C−C=C−、−C=N−C=C−、−N=C−C=N−、−C=N−N=C−または−C=N−C=N−または−C=C−C=C−を形成し、この場合それぞれ−C=および−N−は、全ての他の−C=および−N−とは独立にH、F、オキソ、チオキソ、C1〜C8アルキルまたはOC1〜C8アルキルによって置換されており;
または2個のジェミナルまたはビシナルR9は、一緒になって、それぞれ置換されていないかまたは1回または数回オキソまたはチオキソによって置換された、C3〜C8アルキレンまたはC3〜C8アルケニレン基を形成し、この場合0、1または2個のノンビシナルメチレン単位は、O、SまたはN(C1〜C8アルキル)によって置換されていてよい、黒色着色剤、好ましくは黒色顔料を製造する方法。 - R3、R5およびR7は、Hであり、R4およびR6は、互いに独立にH、F、Br、Cl、COOH、COOR8、CONH2、CONHR8、CONR8R8、CN、COR8、SO3H、SO2Cl、SO2NH2、SO2NHR8、SO2NR8R8、SO2R8、NO2、R8、OR8またはNHCOR8であり、またはR5およびR6は、一緒になって1,4−ブタジエニレン基を形成する、請求項1記載の方法。
- 黒色着色剤を製造する方法において、式
R10は、H、CH3、C2H5、OCH3、OC2H5、F、Cl、Br、NO2、CN、COOHまたはSO3Hであり、
R11は、H、NO2、CN、COOHまたはSO3Hであり、および
R12は、H、CH3、C2H5、OCH3、OC2H5、FまたはClである〕〕で示される2〜5つの化合物とを、1:2の全体のモル比(i):(iv)で、水中で25℃で4.5以下のpKを有する触媒の存在下で反応させ、この場合式(iv)の化合物の1つの量は、式(iv)の全ての化合物の全体量に対して50質量%〜80質量%であることを特徴とする、黒色着色剤を製造する方法。 - R10は、H、CH3、OCH3、F、Cl、Br、NO2またはSO3Hであり、R11は、HまたはSO3Hであり、およびR12は、H、CH3またはClである、請求項3記載の方法。
- 式(ii)、(iv)または(v)の化合物は、次の置換基パターン:
R3=R4=R5=R6=R7=H;
R3=R5=R6=R7=H、R4=NO2;
R3=R5=R6=R7=H、R4=OCH3;
R3=R5=R6=R7=H、R4=Cl;
R3=R5=R6=R7=H、R4=F;
R3=R5=R6=R7=H、R4=Br;
R3=R5=R6=R7=H、R4=SO3H;
R3=R5=R6=R7=H、R4=COOH;
R3=R5=R6=R7=H、R4=N(CH3)2;
R3=R5=R6=R7=H、R4=NHCOC1〜C18アルキル、特にNHCOC1〜C12アルキル;
R3=R5=R6=R7=H、R4=C1〜C20アルキル、特にC1〜C14アルキル;
R3=R5=R6=R7=H、R4=C2〜C20アルコキシ、特にC2〜C14アルコキシ;
R3=R5=R7=H、R4=R6=CH3;
R3=R5=R7=H、R4=R6=Cl;
R3=R5=R7=H、R4=Cl、R6=CH3;
R3=R4=R5=R6=H、R7=CH3;
R3=R4=R5=R6=H、R7=C6H5;および
R3=R4=R7=H、一緒になったR5とR6=1,4−ブタジエニレンを有する化合物から構成されている群から選択される、請求項1、2、3、4、5または6に記載の方法。 - 反応は、式(i)の化合物1モル当たり触媒5・10-3〜5モル%を用いて2・102〜2・106Paの圧力、20〜250℃の温度および1/2〜100時間の反応時間で行なわれる、請求項1、2、3、4、5、6または7に記載の方法。
- 黒色着色剤は、有利に凝集されていない顔料粒子から構成され、10nm〜10μmの平均粒径Lによって特徴付けられ、この場合好ましくは、粒子の60質量%〜100質量%、よりいっそう好ましくは80質量%〜100質量%は、L±1/2Lの粒径を有する、請求項1、2、3、4、5、6、7または8に記載の方法。
- 7.8s、10.2w、12.6s、18.6w、21.8w、22.4w、24.4m、25.0w、26.7m、27.2mおよび28.8w °2Θで線を有するX線粉末回折図によって特徴付けられた、実験式C26H12N2O6のモル比1:2での
6.6s、13.3w、14.8w、21.6w、24.5w、26.4mおよび28.7w °2Θで線を有するX線粉末回折図によって特徴付けられた、実験式C26H12N2O6のモル比1:2での
7.3s、10.9w、12.7w、14.6w、24.5w、26.4mおよび28.7w °2Θで線を有するX線粉末回折図によって特徴付けられた、実験式C26H12N2O6のモル比1:2での
7.2s、9.7w、11.6w、12.7w、19.2w、20.4w、21.5w、24.3w、25.0w、26.6wおよび28.5w °2Θで線を有するX線粉末回折図によって特徴付けられた、実験式C28H16N2O6のモル比1:2での
6.7w、12.6m、14.1w、15.7w、17.2w、19.6w、23.3w、24.8w、25.4w、27.6s、31.0wおよび34.3w °2Θで線を有するX線粉末回折図によって特徴付けられた、実験式C26H10N4O10のモル比1:2での
6.6s、9.7w、13.3w、16.2w、19.9w、22.1w、24.9w、26.9wおよび29.1w °2Θで線を有するX線粉末回折図によって特徴付けられた、実験式C26H10N4O10のモル比1:2での
7.0s、10.1m、11.8s、20.5m、21.8m、24.2m、26.3sおよび27.9m °2Θで線を有するX線粉末回折図によって特徴付けられた、実験式C28H16N2O8のモル比1:2での
6.2s、13.3m、17.8w、22.8w、23.0w、25.0wおよび26.9m °2Θで線を有するX線粉末回折図によって特徴付けられた、実験式C28H16N2O8のモル比1:2での
7.1m、11.7s、19.2w、20.5w、22.6m、24.3m、25.6w、26.7m、27.1mおよび29.0w °2Θで線を有するX線粉末回折図によって特徴付けられた、実験式C26H10N2O6Cl2のモル比1:2での
4.8m、12.6m、21.8w、24.9mおよび27.4s °2Θで線を有するX線粉末回折図によって特徴付けられた、実験式C26H10N2O6Cl2のモル比1:2での
4.7s、9.3w、14.5w、16.0w、19.7wおよび24.6w °2Θで線を有するX線粉末回折図によって特徴付けられた、実験式C26H10N2O6Cl2のモル比1:2での
5.9w、15.2w、23.9w、25.1mおよび26.8s °2Θで線を有するX線粉末回折図によって特徴付けられた、実験式C26H8N2O6Cl4のモル比1:2での
23.9wおよび26.9s °2Θで線を有するX線粉末回折図によって特徴付けられた、実験式C26H8N2O6Cl4のモル比1:2での
6.7s、14.8m、16.1m、19.9m、21.8m、22.3m、24.8m、26.8sおよび29.1m °2Θで線を有するX線粉末回折図によって特徴付けられた、実験式C26H10N2O6F2のモル比1:2での
6.7s、9.7W、13.3W、14.9W、16.3W、20.0W、22.3W、25.0W、26.9Wおよび29.2W °2Θで線を有するX線粉末回折図によって特徴付けられた、実験式C26H10N2O6F2のモル比1:2での
10.0w、11.6m、19.3m、20.6w、22.1s、23,3w、24.3m、25.4m、26.0w、26.9s、28.8wおよび31.3w °2Θで線を有するX線粉末回折図によって特徴付けられた、実験式C26H10N2O6Br2のモル比1:2での
6.0m、7.0m、9.2w、11.1s、19.7w、20.6m、22.4w、25.0m、26.5sおよび28.3w °2Θで線を有するX線粉末回折図によって特徴付けられた、実験式C28H14N2O6Cl2のモル比1:2での
6.7s、9.6w、10.7w、14.4w、15.2w、19.9w、21.6wおよび25.3w °2Θで線を有するX線粉末回折図によって特徴付けられた、実験式C38H20N2O6のモル比1:2での
8.5s、10.7w、12.6w、13.2w、21.0w、21.9w、22.7w、24.5w、26.9wおよび28.6w °2Θで線を有するX線粉末回折図によって特徴付けられた、実験式C28H16N2O6のモル比1:2での
6.9s、9.2w、11.1s、14.2w、20.3w、22.4wおよび26.3m °2Θで線を有するX線粉末回折図によって特徴付けられた、実験式C30H20N2O6のモル比1:2でのトルエン中p−トルエンスルホン酸を用いる、
6.9s、11.0s、20.3wおよび26.3m °2Θで線を有するX線粉末回折図によって特徴付けられた、実験式C30H20N2O6のモル比1:2での
10.6s、14.4w、16.7w、19.1w、23.7w、25.2w、26.6wおよび27.9w °2Θで線を有するX線粉末回折図によって特徴付けられた、実験式C30H16N2O10のモル比1:2での
7.9w、9.7w、11.5w、12.6s、13.5w、15.9w、19.6w、21.4m、22.8w、23.5w、24.0w、25.4m、25.6s、27.9w、28.3w、29.1wおよび30.7w °2Θで線を有するX線粉末回折図によって特徴付けられた、実験式C28H16N2O12S2のモル比1:2での
分子イオンピークm/z 548.1を有する質量スペクトルによって特徴付けられた、実験式C34H16N2O6のモル比1:2での
- 7.6s、9.5w、11.8s、20.7w、24.7m、26.4mおよび28.4m °2Θで線を有するX線粉末回折図によって特徴付けられた、実験式C26H12N2O6、C28H16N2O6およびC30H20N2O6の複数の化合物を有する、モル比1:1:1での
7.4s、10.0w、11.9s、18.8w、20.1w、22.1w、24.1m、25.0w、26.6mおよび28.6w °2Θで線を有するX線粉末回折図によって特徴付けられた、実験式C26H12N2O6、C27H14N2O6およびC28H16N2O6の複数の化合物を有する、モル比1:1:1での
7.2s、9.3w、11.3s、19.4w、20.6w、24.5w、26.4m、26.9wおよび28.3w °2Θで線を有するX線粉末回折図によって特徴付けられた、実験式C28H16N2O6、C29H18N2O6およびC30H20N2O6の複数の化合物を有する、モル比1:1:1での
7.2s、7.4s、10.3w、11.9m、12.2s、13.3w、18.9w、20.2w、22.8m、24.1s、25.3w、26.8sおよび29.0m °2Θで線を有するX線粉末回折図によって特徴付けられた、実験式C26H12N2O6、C26H11N2O6ClおよびC26H10N2O6Cl2の複数の化合物を有する、モル比1:1:1での
7.1s、11.6s、19.2w、20.4w、21.9w、24.2m、25.2w、26.7sおよび28.7w °2Θで線を有するX線粉末回折図によって特徴付けられた、実験式C26H10N2O6Cl2、C27H13N2O6ClおよびC28H16N2O6の複数の化合物を有する、モル比1:1:1での
6.6s、13.5w、14.7m、15.9w、19.8m、21.6m、22.3w、24.6m、26.6sおよび28.8m °2Θで線を有するX線粉末回折図によって特徴付けられた、実験式C26H12N2O6、C26H11N2O6FおよびC26H10N2O6F2の複数の化合物を有する、モル比1:1:1での
7.1m、10.2m、11.8s、13.1w、18.8m、20.2m、22.7s、24.0s、25.3m、26.5s、26.8sおよび28.8m °2Θで線を有するX線粉末回折図によって特徴付けられた、実験式C26H12N2O6、C26H11N2O6BrおよびC26H10N2O6Br2の複数の化合物を有する、モル比1:1:1での
7.0s、10.4w、11.6m、19.0w、20.3w、22.3w、24.0w、25.3w、26.5mおよび28.7w °2Θで線を有するX線粉末回折図によって特徴付けられた、実験式C26H12N2O6、C27H14N2O7およびC28H16N2O8の複数の化合物を有する、モル比1:1:1での
6.1m、11.9m、13.5w、15.0w、16.5w、22.6w、24.1w、24.7wおよび26.9s °2Θで線を有するX線粉末回折図によって特徴付けられた、実験式C26H10N2O6Cl2、C26H10N3O8ClおよびC26H10N4O10の複数の化合物を有する、モル比1:1:1での
4.6s、9.3w、11.6m、14.2w、17.1w、18.8w、22.1w、25.4m、26.0mおよび27.5s °2Θで線を有するX線粉末回折図によって特徴付けられた、実験式C26H10N2O6Cl2、C26H9N2O6Cl3およびC26H8N2O6Cl4の複数の化合物を有する、モル比1:1:1での
7.0s、11.2s、12.7w、19.4w、20.7w、21.6w、22.5w、24.3w、25.3w、26.8mおよび28.7w °2Θで線を有するX線粉末回折図によって特徴付けられた、実験式C26H10N2O6Cl2、C27H13N2O7ClおよびC28H16N2O8の複数の化合物を有する、モル比1:1:1での
- ペイント、印刷用インクおよびプラスチックを全体として着色するための、請求項1、2、3、4、5、6、7、8または9の記載により得られる黒色着色剤の使用、請求項10または11記載の黒色着色剤の使用、または請求項12記載の黒色着色剤組成物の使用。
- 他の結晶の多形態が着色剤の全ての結晶の多形態の全体量に対して20質量%未満、好ましくは10質量%未満の量で存在する、請求項13記載の黒色着色剤の使用。
- 請求項1、2、3、4、5、6、7、8または9の記載により得られる黒色着色剤、請求項10、11または13に記載の黒色着色剤または請求項12記載の黒色着色剤組成物を、全体の着色された高分子量材料に対して0.01質量%〜70質量%含有する、練込み着色された高分子量材料。
- それぞれ着色された全体の高分子量材料に対して、請求項1、2、3、4、5、6、7、8または9の記載により得られる黒色着色剤、請求項10または11に記載の黒色着色剤または請求項12記載の黒色着色剤組成物0.01質量%〜70質量%、好ましくは0.05質量%〜30質量%および塩基性光安定剤または塩基性光安定剤の混合物0.01質量%〜20質量%、好ましくは0.1質量%〜10質量%、よりいっそう好ましくは0.2質量%〜5質量%を含有する、練込み着色された高分子量材料。
- 請求項15または16に記載の練込み着色された高分子量材料を有し、好ましくは請求項15または16に記載の練込み着色された高分子量材料および場合によっては体質顔料および/または補強材料を含有する、マルチングフィルム、インストルメント・パネルまたは織物、庭園家具製品または構造物工業用要素。
- 請求項1、2、3、4、5、6、7、8または9の記載により得られる黒色着色剤、請求項10または11に記載の黒色着色剤または請求項12記載の黒色着色剤組成物がスルホン化されるか、クロロスルホン化されるか、カルボキシル基またはスルホ基で中和されるか、またはSO2Cl基でアミド化される、着色剤の製造法。
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP09150817.6 | 2009-01-19 | ||
EP09150817 | 2009-01-19 | ||
PCT/EP2009/067953 WO2010081625A2 (en) | 2009-01-19 | 2009-12-28 | Organic black pigments and their preparation |
Publications (3)
Publication Number | Publication Date |
---|---|
JP2012515234A true JP2012515234A (ja) | 2012-07-05 |
JP2012515234A5 JP2012515234A5 (ja) | 2013-02-21 |
JP5675647B2 JP5675647B2 (ja) | 2015-02-25 |
Family
ID=40902194
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2011545661A Active JP5675647B2 (ja) | 2009-01-19 | 2009-12-28 | 有機黒色顔料およびその製造 |
Country Status (7)
Country | Link |
---|---|
US (1) | US8691002B2 (ja) |
EP (1) | EP2387600B1 (ja) |
JP (1) | JP5675647B2 (ja) |
KR (1) | KR101773621B1 (ja) |
CN (1) | CN102292397B (ja) |
ES (1) | ES2463674T3 (ja) |
WO (1) | WO2010081625A2 (ja) |
Cited By (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2014103628A1 (ja) | 2012-12-27 | 2014-07-03 | 富士フイルム株式会社 | カラーフィルタ用組成物、赤外線透過フィルタ及びその製造方法、並びに赤外線センサー |
WO2014208348A1 (ja) * | 2013-06-24 | 2014-12-31 | 東レ株式会社 | タッチパネル用黒色樹脂組成物 |
WO2017158914A1 (ja) | 2016-03-14 | 2017-09-21 | 富士フイルム株式会社 | 組成物、膜、硬化膜、光学センサおよび膜の製造方法 |
WO2019054281A1 (ja) | 2017-09-15 | 2019-03-21 | 富士フイルム株式会社 | 組成物、膜、積層体、赤外線透過フィルタ、固体撮像素子および赤外線センサ |
WO2020049930A1 (ja) | 2018-09-07 | 2020-03-12 | 富士フイルム株式会社 | 車両用ヘッドライトユニット、ヘッドライト用の遮光膜、ヘッドライト用の遮光膜の製造方法 |
WO2020059509A1 (ja) | 2018-09-20 | 2020-03-26 | 富士フイルム株式会社 | 硬化性組成物、硬化膜、赤外線透過フィルタ、積層体、固体撮像素子、センサ、及び、パターン形成方法 |
WO2021039205A1 (ja) | 2019-08-29 | 2021-03-04 | 富士フイルム株式会社 | 組成物、膜、近赤外線カットフィルタ、パターン形成方法、積層体、固体撮像素子、赤外線センサ、画像表示装置、カメラモジュール、及び、化合物 |
WO2022130773A1 (ja) | 2020-12-17 | 2022-06-23 | 富士フイルム株式会社 | 組成物、膜、光学フィルタ、固体撮像素子、画像表示装置および赤外線センサ |
WO2022131191A1 (ja) | 2020-12-16 | 2022-06-23 | 富士フイルム株式会社 | 組成物、膜、光学フィルタ、固体撮像素子、画像表示装置および赤外線センサ |
WO2022210175A1 (ja) | 2021-03-29 | 2022-10-06 | 富士フイルム株式会社 | 黒色感光性組成物、黒色感光性組成物の製造方法、硬化膜、カラーフィルタ、遮光膜、光学素子、固体撮像素子、ヘッドライトユニット |
Families Citing this family (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102282216B (zh) | 2009-01-19 | 2014-05-14 | 巴斯夫欧洲公司 | 黑色颜料分散体 |
KR101939419B1 (ko) | 2010-12-30 | 2019-01-16 | 바스프 에스이 | 표면-개질된 안료 제제 |
US10048528B2 (en) | 2014-11-19 | 2018-08-14 | Samsung Sdi Co., Ltd. | Liquid crystal display |
KR102014107B1 (ko) | 2015-05-01 | 2019-08-26 | 후지필름 가부시키가이샤 | 막, 막의 제조 방법, 고체 촬상 소자 및 적외선 센서 |
CN105949442A (zh) * | 2016-03-31 | 2016-09-21 | 合肥工业大学 | 基于(2-氧吲哚-3-亚基)苯并二呋喃-二酮和连噻吩的共轭聚合物的新型聚合方法 |
KR101876198B1 (ko) | 2016-11-28 | 2018-07-10 | 씨큐브 주식회사 | 천연 숯을 이용한 흑색계의 진주 광택 안료의 제조 방법 |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH08510441A (ja) * | 1992-11-25 | 1996-11-05 | ゼネカ・リミテッド | 化合物 |
JP2000504053A (ja) * | 1996-02-01 | 2000-04-04 | ビーエーエスエフ アクチェンゲゼルシャフト | ベンゾジフラノン染料の製造方法 |
JP2002528448A (ja) * | 1998-10-22 | 2002-09-03 | チバ スペシャルティ ケミカルズ ホールディング インコーポレーテッド | オキソベンゾフラニリデン−ジヒドロインドロン類 |
JP2003512996A (ja) * | 1999-11-03 | 2003-04-08 | チバ スペシャルティ ケミカルズ ホールディング インコーポレーテッド | 着色ガラス質材料、それに被覆されているその前駆体ガラス製物品及びその調製方法 |
JP2010534726A (ja) * | 2007-07-19 | 2010-11-11 | ビーエーエスエフ ソシエタス・ヨーロピア | ビス−オキソジヒドロインドリレン−ベンゾジフラノンを含むnir不活性基体 |
Family Cites Families (259)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CH93487A (de) | 1920-12-11 | 1922-03-01 | Staudinger Hermann Dr Prof | Verfahren zur Herstellung einer heterocyclischen Verbindung der Naphtalinreihe. |
US3118887A (en) | 1961-03-06 | 1964-01-21 | American Cyanamid Co | O-hydroxy substituted tris aryl-s-triazines |
US3113942A (en) | 1961-07-13 | 1963-12-10 | Monsanto Res Corp | Mono-alkyl ethers of tris (2-hydroxyphenyl) triazines |
US3113940A (en) | 1961-07-13 | 1963-12-10 | Monsanto Res Corp | Aromatic partial ethers of tris (2-hydroxyphenyl) triazine |
US3113941A (en) | 1961-07-13 | 1963-12-10 | Monsanto Res Corp | Esters of hydroxyaryltriazines |
NL130888C (ja) | 1961-12-21 | |||
NL123744C (ja) | 1962-10-30 | |||
CH484695A (de) | 1962-10-30 | 1970-01-31 | Ciba Geigy | Verwendung von neuen Hydroxyphenyl-1,3,5-triazinen als Ultraviolettschutzmittel ausserhalb der Textilindustrie |
CH480091A (de) | 1962-10-30 | 1969-10-31 | Ciba Geigy | Verwendung von neuen Hydroxyphenyl-1,3,5-triazinen als Ultraviolettschutzmittel ausserhalb der Textilindustrie |
CH480090A (de) | 1962-10-30 | 1969-10-31 | Ciba Geigy | Verwendung von neuen Hydroxyphenyl-1,3,5-triazinen als Ultraviolettschutzmittel ausserhalb der Textilindustrie |
NL130993C (ja) | 1963-02-07 | |||
CH448083A (de) | 1963-05-04 | 1967-12-15 | Ciba Geigy | Verwendung von neuen Hydroxyaryl-pyrimidinen bei Verfahren zum Schützen von nicht-textilen organischen Materialien |
CH469053A (de) | 1963-07-26 | 1969-02-28 | Ciba Geigy | Verwendung von neuen Hydroxyphenyl-1,3,5-triazinen als Schutzmittel gegen Ultraviolettstrahlung für nichttextile organische Materialien |
CH485484A (de) | 1964-12-04 | 1970-02-15 | Ciba Geigy | Verwendung von neuen Hydroxyphenyl-1,3,5-triazinen als Schutzmittel gegen Ultraviollettstrahlung für organische Materialien ausserhalb der Textilindustrie |
CH478589A (de) | 1965-09-24 | 1969-09-30 | Ciba Geigy | Verwendung von Aryl-1,3,5-triazinen als Stabilisierungsmittel gegen Ultraviolettstrahlung und Hitzeeinwirkung ausserhalb der Textilindustrie |
US3535318A (en) | 1967-03-13 | 1970-10-20 | American Cyanamid Co | Mono - aromatic - pentaalkyl ethers of hexamethylolmelamine crease-proofing agents |
US3496134A (en) | 1967-06-20 | 1970-02-17 | American Cyanamid Co | Stabilization of rigid poly(vinylchloride) plastics with bis-amides and ultraviolet absorbers |
US3641213A (en) | 1969-02-27 | 1972-02-08 | American Cyanamid Co | Synergistic uv absorber combination for polypropylene-polyvinylpyridine blend |
CH533853A (de) | 1970-03-23 | 1973-02-15 | Ciba Geigy Ag | Verwendung von 2'-Hydroxyphenyl-1,3,5-triazinen als Stabilisierungsmittel gegen Ultraviolettstrahlung in photographischem Material |
CH557693A (de) | 1971-06-23 | 1975-01-15 | Ciba Geigy Ag | Verfahren zum schuetzen von organischen materialien gegen ultraviolettstrahlung. |
JPS5038133B2 (ja) | 1971-09-17 | 1975-12-08 | ||
FR2363133A1 (fr) | 1977-05-10 | 1978-03-24 | Agfa Gevaert | Colorants chromogenes dont la molecule comprend une fraction absorbant les rayons ultraviolets |
US4186108A (en) | 1978-02-08 | 1980-01-29 | Minnesota Mining And Manufacturing Company | Liquid compositions containing triarylsulfonium complex salts and oxyethylene material |
EP0165608B1 (de) | 1984-06-22 | 1991-01-02 | Ilford Ag | Hydroxyphenyltriazine, Verfahren zu ihrer Herstellung und ihre Verwendung als UV-Absorber |
AU573053B2 (en) | 1984-12-07 | 1988-05-26 | Commonwealth Scientific And Industrial Research Organisation | Sulfonated triazine as photostabilisers on fibres and leather |
US4619956A (en) | 1985-05-03 | 1986-10-28 | American Cyanamid Co. | Stabilization of high solids coatings with synergistic combinations |
US4831068A (en) | 1987-02-27 | 1989-05-16 | Ciba-Geigy Corporation | Process for improving the photochemical stability of dyeings on polyester fibre materials |
EP0280654B1 (de) | 1987-02-27 | 1992-05-13 | Ciba-Geigy Ag | Verfahren zur Verbesserung der fotochemischen Stabilität von Färbungen auf Polyesterfasermaterialien |
US4950304A (en) | 1987-10-02 | 1990-08-21 | Ciba-Geigy Corporation | Process for quenching or suppressing the fluorescence of substrates treated with fluorescent whitening agents |
JPH0718585B2 (ja) | 1987-11-19 | 1995-03-06 | 松下電器産業株式会社 | 空気調和機の遠隔操作装置 |
US4826978A (en) | 1987-12-29 | 1989-05-02 | Milliken Research Corporation | Reactive, non-yellowing triazine compounds useful as UV screening agents for polymers |
EP0345212A1 (de) | 1988-05-04 | 1989-12-06 | Ciba-Geigy Ag | Verfahren zur Verhinderung der Vergilbung von mit Fleckenschutzmitteln ausgerüsteten Polyamidfasermaterialien |
DE3815622A1 (de) | 1988-05-07 | 1989-11-16 | Merck Patent Gmbh | Fotoinitiator-dispersionen |
EP0357545A3 (de) | 1988-07-21 | 1990-03-21 | Ciba-Geigy Ag | Kationische Verbindungen, deren Herstellung und deren Anwendung zur fotochemischen Stabilisierung basisch anfärbbarer Polyamid-, Polyacrylnitril-und Polyesterfasermaterialien |
DE59010061D1 (de) | 1989-04-21 | 1996-02-29 | Ciba Geigy Ag | Verfahren zur Herstellung von 2-(2',4'-Dihydroxyphenyl)-4,6-diaryl-s-triazinen |
EP0425429B1 (de) | 1989-08-25 | 1995-02-22 | Ciba-Geigy Ag | Lichtstabilisierte Tinten |
US5231135A (en) | 1989-09-05 | 1993-07-27 | Milliken Research Corporation | Lightfast colored polymeric coatings and process for making same |
DE69030362T2 (de) | 1989-12-05 | 1997-10-23 | Ciba Geigy Ag | Stabilisiertes organisches Material |
ES2077052T3 (es) | 1989-12-21 | 1995-11-16 | Ciba Geigy Ag | Procedimiento para la incorporacion de o-hidroxifenil-s-triazinas a polimeros organicos. |
US5759700A (en) | 1989-12-26 | 1998-06-02 | Cytec Technology Corp. | Stabilization of high solids coatings with liquid compositions of triazine UV absorbers |
EP0441746B1 (de) | 1990-02-06 | 1995-06-21 | Ciba-Geigy Ag | Lichtstabilisierte Bindemittel für Lacke |
EP0442847B2 (de) | 1990-02-16 | 2000-08-23 | Ciba SC Holding AG | Gegen Schädigung durch Licht, Wärme und Sauerstoff stabilisierte Ueberzugsmittel |
ATE150458T1 (de) | 1990-02-28 | 1997-04-15 | Cytec Tech Corp | Stabilisierung von überzügen mit hohem festkörpergehalt mit flüssigen zusammenstellungen von uv absorbierenden triazinen |
DE59107052D1 (de) | 1990-03-30 | 1996-01-25 | Ciba Geigy Ag | Lackzusammensetzungen |
DE59109192D1 (de) | 1990-04-20 | 2000-08-17 | Ciba Sc Holding Ag | Verbindungen aus o-Hydroxyphenyl-1,3,5-triazinen und sterisch gehinderten Aminen |
DE59107294D1 (de) | 1990-05-10 | 1996-03-07 | Ciba Geigy Ag | Strahlenhärtbare lichtstabilisierte Zusammensetzungen |
DE59108599D1 (de) | 1990-05-31 | 1997-04-17 | Ciba Geigy | Stabilisierung von Färbungen auf Polyamidfasern |
DE59106971D1 (de) | 1990-07-12 | 1996-01-11 | Ciba Geigy Ag | Verfahren zur photochemischen und thermischen Stabilisierung von Polyamid-Fasermaterialien. |
DE59105836D1 (de) | 1990-07-23 | 1995-08-03 | Ciba Geigy Ag | Wässrige Dispersion schwerlöslicher UV-Absorber. |
EP0483488B1 (en) | 1990-10-29 | 1997-03-12 | Cytec Technology Corp. | Synergistic ultraviolet absorber compositions containing hydroxy aryl triazines and tetraalkyl piperidines |
DE59209837D1 (de) | 1991-01-31 | 2000-06-15 | Ciba Sc Holding Ag | Verfahren zur Herstellung von 2-(2',4'-Dihydroxyphenyl)-4,6-diaryl-s-triazinen |
KR100187320B1 (ko) | 1991-02-21 | 1999-04-01 | 월터 클리웨인 | 광, 산소 및 열에 대해 안정화된 도료 |
TW222292B (ja) | 1991-02-21 | 1994-04-11 | Ciba Geigy Ag | |
EP0502821B1 (de) | 1991-03-05 | 1996-01-31 | Ciba-Geigy Ag | Silylierte 2-(2-Hydroxyphenyl)-4,6-diaryl-1,3,5-triazine |
EP0506615B1 (de) | 1991-03-27 | 1995-02-22 | Ciba-Geigy Ag | Stabilisierte Methylmethacrylat-Polymere |
EP0512946B1 (de) | 1991-05-02 | 1995-09-13 | Ciba-Geigy Ag | Verfahren zur Verbesserung der Lichtechtheit von Leder |
DE59208921D1 (de) | 1991-06-03 | 1997-10-30 | Ciba Geigy Ag | UV-Absorber enthaltendes photographisches Material |
EP0530135A1 (de) | 1991-06-03 | 1993-03-03 | Ciba-Geigy Ag | UV-Absorber enthaltendes photographisches Material |
DK0523006T3 (da) | 1991-07-12 | 1995-12-27 | Ciba Geigy Ag | Fremgangsmåde til trykning og fotokemisk stabilisering af polyesterfibermaterialer |
DE59203814D1 (de) | 1991-07-29 | 1995-11-02 | Ciba Geigy Ag | Lichtstabilisierte Copolymer-Zusammensetzungen als Bindemittel für Lacke. |
DE59208885D1 (de) | 1991-09-05 | 1997-10-16 | Ciba Geigy Ag | UV-Absorber enthaltendes photographisches Material |
EP0546993A1 (de) | 1991-12-09 | 1993-06-16 | Ciba-Geigy Ag | Wasserlöschliche Triazinderivate zur photochemischen und thermischen Stabilisierung von Polyamidfasermaterialien |
EP0555180A1 (de) | 1992-02-04 | 1993-08-11 | Ciba-Geigy Ag | Verfahren zur Herstellung von 2-Hydroxy-4,6-diaryl-1,3,5-triazinen |
DE59303910D1 (de) | 1992-02-13 | 1996-10-31 | Ciba Geigy Ag | Verfahren zur Herstellung von 2-Hydroxy-4,6-diaryl-1,3,5-triazin |
US5298030A (en) | 1992-02-21 | 1994-03-29 | Ciba-Geigy Corporation | Process for the photochemical and thermal stabilization of undyed and dyed or printed polyester fiber materials |
TW252111B (ja) | 1992-07-02 | 1995-07-21 | Ciba Geigy | |
SE500609C2 (sv) | 1992-07-09 | 1994-07-25 | Asea Brown Boveri | Lindningskopplare |
ATE155538T1 (de) | 1992-08-18 | 1997-08-15 | Ciba Geigy Ag | Verfahren zur photochemischen und thermischen stabilisierung von ungefärbten und gefärbten polyesterfasermaterialien |
JP3800344B2 (ja) | 1992-09-07 | 2006-07-26 | チバ スペシャルティ ケミカルズ ホールディング インコーポレーテッド | ヒドロキシフェニル−s−トリアジン |
US5489503A (en) | 1992-12-03 | 1996-02-06 | Ciba-Geigy Corp. | UV absorbers |
DE59310205D1 (de) | 1992-12-17 | 2001-10-11 | Ciba Sc Holding Ag | Kationische Verbindungen, deren Herstellung und deren Anwendung zur fotochemischen Stabilisierung basisch anfärbbarer Polyamidfasermaterialien |
US5621052A (en) | 1992-12-29 | 1997-04-15 | Cytec Technology Corp. | Aminoplast-anchored ultraviolet light stabilizers |
EP0618205A1 (de) | 1993-04-02 | 1994-10-05 | Ciba-Geigy Ag | Wasserlösliche Triazinderivate zur photochemischen und thermischen Stabilisierung von Polyamidfasermaterialien |
EP0621266A1 (de) | 1993-04-22 | 1994-10-26 | Ciba-Geigy Ag | Sterisch gehinderte Phenole und ihre Verwendung zur Stabilisierung von Polyamid-Fasermaterialen |
US6706215B1 (en) | 1993-05-17 | 2004-03-16 | Ciba Specialty Chemicals Corporation | Coating compositions stabilized against damage by light, heat and oxygen |
GB2278115B (en) | 1993-05-17 | 1997-08-06 | Ciba Geigy Ag | 2-(2-Hydroxyphenyl)-1,3-pyrimidine derivatives and their use as stabilizers for coating compositions |
JPH07134360A (ja) | 1993-09-14 | 1995-05-23 | Konica Corp | ハロゲン化銀写真感光材料及び画像形成方法 |
CH686305A5 (de) | 1993-09-28 | 1996-02-29 | Ciba Geigy Ag | Verfahren zur Herstellung von 1,3,5-Triazinen. |
EP0648754B1 (de) | 1993-10-15 | 2000-07-12 | Ciba SC Holding AG | Verfahren zur Herstellung von Hydroxyphenyl-1,3,5-Triazinen |
TW254936B (ja) | 1993-10-22 | 1995-08-21 | Ciba Geigy | |
JP3111302B2 (ja) | 1993-11-22 | 2000-11-20 | 富士写真フイルム株式会社 | ハロゲン化銀カラー写真感光材料 |
EP0654469B1 (de) | 1993-11-23 | 2001-08-22 | Ciba SC Holding AG | o-Hydroxyphenyl-s-triazine enthaltende stabilisierte Polymere |
GB9326358D0 (en) | 1993-12-23 | 1994-02-23 | Ciba Geigy Ag | Compositions for the treatment of textiles |
ATE180283T1 (de) | 1994-01-19 | 1999-06-15 | Ciba Geigy Ag | Stabilisieren von leder gegen thermische und photochemische zersetzung |
GB9403451D0 (en) | 1994-02-23 | 1994-04-13 | Ciba Geigy Ag | Sunscreen compositions |
DE59509569D1 (de) | 1994-04-26 | 2001-10-11 | Ciba Sc Holding Ag | Kationische oder basische Aminobenzthiazol-Farbstoffe |
GB9409466D0 (en) | 1994-05-12 | 1994-06-29 | Ciba Geigy Ag | Textile treatment |
DE69533417T2 (de) | 1994-05-12 | 2005-08-18 | Ciba Specialty Chemicals Holding Inc. | Textilbehandlungen |
GB2290745A (en) | 1994-07-01 | 1996-01-10 | Ciba Geigy Ag | Coextruded stabilised laminated thermolastics |
US5741905A (en) | 1994-07-23 | 1998-04-21 | Ciba Specialty Chemicals Corporation | Triazine ultraviolet absorbers useful for improving the sun protection factor of textiles |
GB2291658B (en) | 1994-07-23 | 1998-08-12 | Ciba Geigy Ag | Aqueous textile treatment compositions containing an ultra-violet absorbing agent |
US5556973A (en) | 1994-07-27 | 1996-09-17 | Ciba-Geigy Corporation | Red-shifted tris-aryl-s-triazines and compositions stabilized therewith |
ES2152374T3 (es) | 1994-09-14 | 2001-02-01 | Ciba Sc Holding Ag | Absorbentes uv, obtencion y utilizacion. |
DE69507235T2 (de) | 1994-09-30 | 1999-07-29 | Ciba Geigy Ag | Stabilisierung von pigmentierten Fasern mit einer synergistischen Mischung von UV-Absorber und gehindertem Amin |
EP0706083A1 (de) | 1994-10-04 | 1996-04-10 | Ciba-Geigy Ag | Fotografisches Aufzeichnungsmaterial enthaltend einen UV-Absorber |
US5672704A (en) | 1994-10-04 | 1997-09-30 | Ciba-Geigy Corporation | 2-Hydroxyphenyl-s-Triazines substituted with ethylenically unsaturated moieties |
AU703967B2 (en) | 1994-10-10 | 1999-04-01 | Ciba Specialty Chemicals Holding Inc. | Bisresorcinyltriazines |
EP0711804A3 (de) | 1994-11-14 | 1999-09-22 | Ciba SC Holding AG | Kryptolichtschutzmittel |
DE4442167A1 (de) | 1994-11-26 | 1996-05-30 | Basf Ag | Witterungsstabile Polyoxymethylenformmassen |
JPH08151480A (ja) | 1994-11-29 | 1996-06-11 | Asahi Denka Kogyo Kk | 耐候性の改善された有機材料組成物 |
JP3548645B2 (ja) | 1994-12-09 | 2004-07-28 | 三善加工株式会社 | 植物の栽培方法 |
DE4444258A1 (de) | 1994-12-13 | 1995-11-23 | Agfa Gevaert Ag | Fotografisches Aufzeichnungsmaterial |
JP3404160B2 (ja) | 1995-01-06 | 2003-05-06 | 旭電化工業株式会社 | メタクリル系ラッカー組成物 |
DE19500441A1 (de) | 1995-01-10 | 1996-07-11 | Agfa Gevaert Ag | Fotografisches Aufzeichnungsmaterial |
JPH08193180A (ja) | 1995-01-18 | 1996-07-30 | Asahi Denka Kogyo Kk | エマルジョン型塗料用組成物 |
TW308601B (ja) | 1995-01-18 | 1997-06-21 | Ciba Sc Holding Ag | |
CN1117086C (zh) | 1995-03-15 | 2003-08-06 | 希巴特殊化学控股公司 | 联苯基取代的三嗪类光稳定剂 |
AU713025B2 (en) | 1995-03-17 | 1999-11-18 | Ciba Specialty Chemicals Holding Inc. | Liposomogenic UV absorbers |
JP3435251B2 (ja) | 1995-03-28 | 2003-08-11 | 旭電化工業株式会社 | 感熱記録材料 |
JPH11503781A (ja) | 1995-04-19 | 1999-03-30 | シエル・インターナシヨネイル・リサーチ・マーチヤツピイ・ベー・ウイ | ポリケトンポリマー組成物 |
EP0743309B1 (de) | 1995-05-18 | 2003-09-10 | Ciba Specialty Chemicals Holding Inc. | o-Hydroxyphenyl-s-triazine als UV-Stabilisatoren |
US5681871A (en) | 1995-05-24 | 1997-10-28 | Johnson & Johnson Vision Products, Inc. | Method for preparing ultraviolet radiation absorbing contact lenses |
TW325490B (en) | 1995-06-23 | 1998-01-21 | Ciba Sc Holding Ag | Polysiloxane light stabilizers |
JP3736814B2 (ja) | 1995-07-05 | 2006-01-18 | 旭電化工業株式会社 | トリアジン系化合物およびそれからなる紫外線吸収剤 |
JPH0922099A (ja) | 1995-07-06 | 1997-01-21 | Fuji Photo Film Co Ltd | ハロゲン化銀カラー写真感光材料 |
GB9515048D0 (en) | 1995-07-22 | 1995-09-20 | Ciba Geigy Ag | Sunscreen compositions |
WO1997003642A1 (en) | 1995-07-22 | 1997-02-06 | Ciba Specialty Chemicals Holding Inc. | Sunscreen compositions |
JPH0952916A (ja) | 1995-08-11 | 1997-02-25 | Asahi Denka Kogyo Kk | 紫外線吸収性組成物 |
JP3844307B2 (ja) | 1995-08-11 | 2006-11-08 | 株式会社Adeka | 2−(2’,4’−ジヒドロキシフェニル)−4,6−ジアリール−s−トリアジン誘導体の製造方法 |
US5585422A (en) | 1995-09-20 | 1996-12-17 | Ciba-Geigy Corporation | Hybrid s-triazine light stabilizers substituted by benzotriazole or benzophenone moieties and compositions stabilized therewith |
DE19536376A1 (de) | 1995-09-29 | 1996-05-15 | Agfa Gevaert Ag | Fotografisches Material |
DE19538950A1 (de) | 1995-10-19 | 1997-04-24 | Agfa Gevaert Ag | Farbfotografisches Silberhalogenidmaterial |
JP3904262B2 (ja) | 1995-11-06 | 2007-04-11 | 旭化成ケミカルズ株式会社 | 積層体 |
DE19541941A1 (de) | 1995-11-10 | 1997-05-15 | Agfa Gevaert Ag | Farbfotografisches Silberhalogenidmaterial |
DE19543730A1 (de) | 1995-11-23 | 1997-05-28 | Ciba Geigy Ag | Bis-Resorcinyl-Triazine |
US5726310A (en) | 1995-12-14 | 1998-03-10 | Ciba Specialty Chemicals Corporation | Process for the preparation of 2-(2,4-dihydroxylphenyl)-4,6-bis(2,4-dimehylphenyl)-s-triazine |
JPH09176476A (ja) | 1995-12-25 | 1997-07-08 | Mitsubishi Gas Chem Co Inc | 耐紫外線性ポリカーボネート樹脂組成物 |
JP3705554B2 (ja) | 1996-01-19 | 2005-10-12 | 旭化成ケミカルズ株式会社 | ポリアセタール樹脂組成物 |
JP3881396B2 (ja) | 1996-02-21 | 2007-02-14 | 関西ペイント株式会社 | クリヤー塗料およびその塗装法 |
EP0795640B1 (de) | 1996-03-13 | 2008-06-18 | Huntsman Advanced Materials (Switzerland) GmbH | Stabilisatorkombination |
CH692739A5 (de) | 1996-03-26 | 2002-10-15 | Ciba Sc Holding Ag | Polymerzusammensetzungen enthaltend 2-Hydroxyphenyl-1,3,5-triazine als UV-Absorber sowie neue 2-Hydroxyphenyl-1,3,5-triazine |
GB9606970D0 (en) | 1996-04-02 | 1996-06-05 | Ciba Geigy Ag | Compounds |
US5770115A (en) | 1996-04-19 | 1998-06-23 | Ppg Industries, Inc. | Photochromic naphthopyran compositions of improved fatigue resistance |
DE19619946A1 (de) | 1996-05-17 | 1997-11-20 | Agfa Gevaert Ag | Farbfotografisches Silberhalogenidmaterial |
JPH101599A (ja) | 1996-06-19 | 1998-01-06 | Mitsubishi Chem Corp | ポリブチレンテレフタレート |
US5962683A (en) | 1996-06-28 | 1999-10-05 | Ciba Specialty Chemicals Corp. | Oxazoline compounds as stabilizers |
JP3727113B2 (ja) | 1996-07-31 | 2005-12-14 | 旭化成ケミカルズ株式会社 | ポリカーボネート積層シート |
JPH1017556A (ja) | 1996-07-03 | 1998-01-20 | Asahi Denka Kogyo Kk | トリアジン系化合物、それからなる紫外線吸収剤およびそれを含む組成物 |
JP3932144B2 (ja) | 1996-07-05 | 2007-06-20 | 株式会社Adeka | トリアジン系化合物、それからなる紫外線吸収剤及びそれを含む高分子材料組成物 |
ES2192688T3 (es) | 1996-07-18 | 2003-10-16 | Ciba Sc Holding Ag | Derivados de benzofenona polioxialquilen sustituidos y puenteados como absorbedores de uv. |
JPH1044357A (ja) | 1996-08-02 | 1998-02-17 | Asahi Chem Ind Co Ltd | 撥水性積層シート |
JPH1044358A (ja) | 1996-08-02 | 1998-02-17 | Asahi Chem Ind Co Ltd | 表面硬化積層シート |
GB9617185D0 (en) | 1996-08-15 | 1996-09-25 | Ici Plc | Polymeric film |
JPH1060212A (ja) | 1996-08-15 | 1998-03-03 | Asahi Chem Ind Co Ltd | 光安定化された帯電防止性アクリル系樹脂組成物 |
US5990188A (en) | 1996-08-15 | 1999-11-23 | General Electric Company | Radiation curable coatings with improved weatherability |
US6004678A (en) | 1996-08-16 | 1999-12-21 | General Electric Company | Low plate out polycarbonate compositions |
EP0824909B1 (de) | 1996-08-23 | 2003-09-10 | Ciba Specialty Chemicals Holding Inc. | Verwendung von ausgewählten Benzotriazol- und Triazinderivaten zum Schützen von menschlichem Haar vor der schädigenden Einwirkung von UV-Strahlung |
US5726309A (en) | 1996-08-27 | 1998-03-10 | Ciba Specialty Chemicals Corporation | Tris-aryls-triazines substituted with biphenylyl groups |
US5998116A (en) | 1996-09-13 | 1999-12-07 | Ciba Specialty Chemicals Corporation | Color-photographic recording material |
DE19739781A1 (de) | 1996-09-13 | 1998-03-19 | Ciba Geigy Ag | Hydroxyphenyltriazine |
BE1012529A3 (fr) | 1996-09-13 | 2000-12-05 | Ciba Sc Holding Ag | Melange de triaryltriazines et son utilisation pour la stabilisation de materiaux organiques. |
JPH10110140A (ja) | 1996-10-07 | 1998-04-28 | Sekisui Chem Co Ltd | 粘着テープの製造方法 |
GB2319523B (en) | 1996-11-20 | 2000-11-08 | Ciba Sc Holding Ag | Hydroxyphenyltriazines |
BR9713109B1 (pt) | 1996-11-20 | 2009-05-05 | preparações cosméticas de derivados simétricos de triazina, para pele ou cabelo e seu uso. | |
US5872165A (en) | 1996-12-18 | 1999-02-16 | Basf Corporation | Coating composition and method for reducing ultraviolet light degradation |
JP2001511823A (ja) | 1996-12-18 | 2001-08-14 | ビーエーエスエフ、コーポレーション | 耐久性増強剤、その方法およびそれを含有するコーティング組成物 |
DE19701719A1 (de) | 1997-01-20 | 1998-07-23 | Agfa Gevaert Ag | Farbfotografisches Aufzeichnungsmaterial mit Silberhalogenidemulsionsschichten und diesen zugeordneten Farbkupplern, das in mindestens eine seiner farbkupplerhaltigen Schichten Zusätze zur Verbesserung der Farbbildstabilität enthält |
DE19701718A1 (de) | 1997-01-20 | 1998-07-23 | Agfa Gevaert Ag | Farbfotografisches Aufzeichnungsmaterial mit Silberhalogenidemulsionsschichten und diesen zugeordneten Farbkupplern, das in mindestens einer seiner farbkupplerhaltigen Schichten Zusätze zur Verbesserung der Farbbildstabilität enthält |
JPH10204284A (ja) | 1997-01-21 | 1998-08-04 | Kyodo Yakuhin Kk | 安定化されたポリウレタン組成物 |
EP0864687A3 (de) | 1997-03-11 | 1999-11-24 | Ciba SC Holding AG | Verfahren zur Verbesserung der photochemischen Stabilität von Färbungen und Drucken auf Polyesterfasern |
EP0870797B1 (en) | 1997-04-07 | 2003-01-29 | Agfa-Gevaert | Polyalkylene naphtalate film comprising specific UV-absorber |
CN1234052A (zh) * | 1997-04-17 | 1999-11-03 | 西巴特殊化学品控股有限公司 | 给体取代的氧靛蓝衍生物和其作为着色剂的用途 |
EP0878469B1 (de) | 1997-05-16 | 2004-10-27 | Ciba SC Holding AG | Resorcinyl-Triazine |
DE19723504C1 (de) | 1997-06-05 | 1998-10-15 | Basf Coatings Ag | Beschichtungsmittel, Verfahren zu seiner Herstellung und seine Verwendung als Decklack oder Klarlack, insbesondere zur Beschichtung von Kunststoffen |
DE19723582A1 (de) | 1997-06-05 | 1998-12-10 | Agfa Gevaert Ag | Fotografisches Aufzeichnungsmaterial mit einem transparenten Schichtträger |
US5840788A (en) | 1997-06-20 | 1998-11-24 | Acushnet Company | Ultraviolet light resistant urethane top coat for golf balls |
BR9811958B1 (pt) | 1997-08-20 | 2010-08-24 | uso de um absorvedor de uv derivado de bis(resorcinil)triazina e formulaÇço cosmÉtica compreendendo o mesmo. | |
US5907026A (en) | 1997-08-27 | 1999-05-25 | General Electric Company | Polycarbonate compositions comprising polyester resins and ultraviolet light absorbers |
JP4070157B2 (ja) | 1997-08-29 | 2008-04-02 | 株式会社Adeka | トリアジン系化合物および紫外線吸収剤 |
JP4070156B2 (ja) | 1997-08-29 | 2008-04-02 | 株式会社Adeka | トリアジン系化合物及び紫外線吸収剤 |
US5869554A (en) | 1997-09-02 | 1999-02-09 | General Electric Company | Polycarbonate compositions comprising hindered amine light stabilizers and ultraviolet light absorbers |
JP4014184B2 (ja) | 1997-10-13 | 2007-11-28 | 株式会社Adeka | 高分子材料組成物 |
US6117997A (en) | 1997-11-19 | 2000-09-12 | Ciba Specialty Chemicals Corporation | Hydroxyphenyltriazines |
ZA9810605B (en) | 1997-11-21 | 1999-05-25 | Cytec Techonoly Corp | Trisaryl-1,3,5-triazine ultraviolet light absorbers |
ZA9810604B (en) | 1997-11-21 | 1999-05-25 | Cytec Tech Corp | Novel trisaryl-1,3,5-triazine ultraviolet light absorbers |
JPH11160840A (ja) | 1997-11-27 | 1999-06-18 | Konica Corp | 紫外線吸収機能を有する写真用カプラー及び該写真用カプラーを用いたハロゲン化銀写真感光材料 |
JPH11174638A (ja) | 1997-12-08 | 1999-07-02 | Konica Corp | ハロゲン化銀カラー写真感光材料 |
EP0937716B1 (de) | 1998-02-20 | 2003-04-09 | Ciba SC Holding AG | Verfahren zur Herstellung von Phenyldichloro-1,3,5-triazinverbindungen |
DE69941073D1 (de) | 1998-03-02 | 2009-08-20 | Ciba Holding Inc | Verfahren zur Herstellung von 2,4-Diaryl-6-o-hydroxyphenyl-1,3,5-triazin Derivaten in Anwesenheit eines Protonensäure-Katalysators |
BR9909461A (pt) * | 1998-04-08 | 2000-12-12 | Ciba Sc Holding Ag | Dibenzonaftironas e o uso das mesmas para colorir ou pigmentar material orgânico de alto peso molecular |
SG75939A1 (en) | 1998-04-09 | 2000-10-24 | Ciba Sc Holding Ag | Diresorcinyl-alkoxy-and-aryloxy-s-triazines |
US6455442B1 (en) | 1998-04-27 | 2002-09-24 | Ciba Specialty Chemicals Corporation | Process for the preparation of UV protective coatings by plasma-enhanced deposition |
US6051164A (en) | 1998-04-30 | 2000-04-18 | Cytec Technology Corp. | Methods and compositions for protecting polymers from UV light |
JP2000026435A (ja) | 1998-05-07 | 2000-01-25 | Ciba Specialty Chem Holding Inc | トリスレゾリシニルトリアジン |
EP0964096A2 (de) | 1998-06-11 | 1999-12-15 | Ciba SC Holding AG | Verfahren zur Verbesserung der photochemischen und thermischen Stabilität von Färbungen und Drucken auf Polyesterfasermaterialien |
DE69924490T2 (de) | 1998-06-22 | 2006-01-19 | Ciba Speciality Chemicals Holding Inc. | Poly-trisaryl-1,3,5-triazin-carbamate als uv-lichtabsorber |
JP2002518487A (ja) | 1998-06-22 | 2002-06-25 | サイテク・テクノロジー・コーポレーシヨン | ベンゾ環置換トリアジン及びピリミジン紫外線吸収剤 |
EP1087947A2 (en) | 1998-06-22 | 2001-04-04 | Ciba SC Holding AG | Trisaryl-1,3,5-triazine ultraviolet light absorbers containing hindered phenols |
AU755175B2 (en) | 1998-06-22 | 2002-12-05 | Cytec Technology Corp. | Non-yellowing para-tertiary-alkyl phenyl substituted triazine ultraviolet light absorbers |
ZA9810599B (en) | 1998-06-22 | 1999-07-30 | Cytec Tech Corp | Triazine UV absorber comprising amino resins. |
CA2336246A1 (en) | 1998-06-22 | 1999-12-29 | Cytec Technology Corp. | Red-shifted trisaryl-1,3,5-triazine ultraviolet light absorbers |
JP3640806B2 (ja) | 1998-07-31 | 2005-04-20 | 大塚化学ホールディングス株式会社 | 転写箔 |
ATE338032T1 (de) | 1998-09-04 | 2006-09-15 | Cytec Tech Corp | 2-(2,4 dihydroxyphenyl)-4,6 bis(3,4- dimethylphenyl)-s-triazine und 2-(2,4- |
WO2000014076A1 (en) | 1998-09-04 | 2000-03-16 | Ciba Specialty Chemicals Holding Inc. | Process for making 2,4-dihydroxyphenyl and 2-hydroxy-4-alkoxyphenyl substituted triazine compounds |
EP1109791B1 (en) | 1998-09-04 | 2004-11-03 | Cytec Technology Corp. | Process for making 2-(2-hydroxy-4-alkoxyphenyl)-4,6-bisaryl-1,3,5-triazines |
AU5789299A (en) | 1998-09-04 | 2000-03-27 | Ciba Specialty Chemicals Holding Inc. | Process for making 2-hydroxy-4-alkoxyphenyl or 2,4-dihydroxyphenyl substituted 1,3,5-triazine uv absorbers |
DE19846971A1 (de) | 1998-10-12 | 2000-04-20 | Basf Coatings Ag | Beschichtungsmittel, Verfahren zu seiner Herstellung und seine Verwendung als Decklack oder Klarlack, insbesondere zur Beschichtung von Kunststoffen |
JP2000136270A (ja) | 1998-10-30 | 2000-05-16 | Dainippon Ink & Chem Inc | 樹脂組成物およびその成形体 |
WO2000025731A1 (en) | 1998-11-02 | 2000-05-11 | Ciba Specialty Chemicals Holding Inc. | Stabilisation of body-care and household products |
WO2000025730A1 (en) | 1998-11-02 | 2000-05-11 | Ciba Specialty Chemicals Holding Inc. | Stabilization of body-care and household products |
TWI259182B (en) | 1998-11-17 | 2006-08-01 | Cytec Tech Corp | Process for preparing triazines using a combination of Lewis acids with reaction promoters |
JP2000154322A (ja) | 1998-11-19 | 2000-06-06 | Grand Polymer:Kk | 難燃性熱可塑性樹脂組成物 |
GB2344596A (en) | 1998-12-09 | 2000-06-14 | Du Pont | Flame retarded and UV light stabilised polyester film |
WO2000039209A1 (en) | 1998-12-23 | 2000-07-06 | Ciba Specialty Chemicals Holding Inc. | Polymeric stabilizers having low polydispersity |
JP4135041B2 (ja) | 1998-12-25 | 2008-08-20 | Dic株式会社 | 樹脂組成物およびその成形体 |
US6392041B1 (en) | 1999-02-25 | 2002-05-21 | Ciba Specialty Chemicals Corporation | Hydroxy-substituted N-alkoxy hindered amines and compositions stabilized therewith |
JP4259697B2 (ja) | 1999-03-02 | 2009-04-30 | 株式会社Adeka | ポリカーボネート樹脂成形物 |
CN1330645C (zh) * | 1999-03-10 | 2007-08-08 | 西巴特殊化学品控股有限公司 | 作为有机材料着色剂的苯并呋喃-2-酮类化合物 |
WO2000061685A1 (fr) | 1999-04-12 | 2000-10-19 | Asahi Denka Kogyo K. K. | Composition de matiere polymere |
US6191199B1 (en) | 1999-05-03 | 2001-02-20 | Ciba Speciatly Chemicals Corporation | Stabilized adhesive compositions containing highly soluble, high extinction photostable hydroxyphenyl-s-triazine UV absorbers and laminated articles derived therefrom |
CN1221244C (zh) | 1999-06-18 | 2005-10-05 | 西巴特殊化学品控股有限公司 | 微细颜料混合物 |
ES2370485T3 (es) | 1999-07-09 | 2011-12-16 | Basf Se | C.i. pigmento red 254 con propiedades colorantes mejoradas. |
EP1068866A3 (de) | 1999-07-12 | 2004-03-17 | Ciba SC Holding AG | Verwendung von Mischungen aus Mikropigmenten zur Bräunungsverhinderung und Aufhellung der Haut und Haare |
JP3968197B2 (ja) | 1999-09-22 | 2007-08-29 | 富士フイルム株式会社 | 画像保存性の改良されたカラー写真感光材料及び写真用塗布組成物 |
DE69931792T2 (de) | 1999-12-01 | 2007-05-16 | Chi Mei Optoelectronics Corp. | UV absorbierender Film und Verwendung als Schutzfolie |
AU779668B2 (en) | 1999-12-23 | 2005-02-03 | Ciba Specialty Chemicals Holding Inc. | Stabilizer mixture |
BR0117305B1 (pt) | 2000-02-01 | 2013-02-05 | mÉtodo de proteÇço de conteédos contra os efeitos prejudiciais de radiaÇço ultravioleta. | |
DE60133181T2 (de) | 2000-02-22 | 2009-03-12 | Ciba Holding Inc. | Stabilisatormischungen für polyolefine |
CA2399871A1 (en) | 2000-02-22 | 2001-08-30 | Ciba Specialty Chemicals Holding Inc. | Romp with oligomeric uv-absorbers |
DE10009286A1 (de) | 2000-02-28 | 2001-08-30 | Mitsubishi Polyester Film Gmbh | Weisse, biaxial orientierte, schwer entflammbare und UV-stabilisierte Polyesterfolie mit Cycloolefincopolymer, Verfahren zu ihrer Herstellung und ihre Verwendung |
DE10009246A1 (de) | 2000-02-28 | 2001-08-30 | Mitsubishi Polyester Film Gmbh | Weiße, biaxial orientierte und UV-stabilisierte Polyesterfolie mit Cycloolefinocopolymer (COC), Verfahren zu ihrer Herstellung und ihre Verwendung |
JP3617802B2 (ja) | 2000-03-30 | 2005-02-09 | 富士写真フイルム株式会社 | 光情報記録媒体及び情報記録方法 |
GB2361005B (en) | 2000-04-04 | 2002-08-14 | Ciba Sc Holding Ag | Synergistic mixtures of uv-absorbers in polyolefins |
WO2001079340A1 (en) | 2000-04-13 | 2001-10-25 | 3M Innovative Properties Company | Light stable articles |
ES2220722T3 (es) | 2000-05-19 | 2004-12-16 | Dow Global Technologies Inc. | Composiciones de polimero de carbonato que comprenden compuestos absorbentes de uv poco volatiles. |
US6297300B1 (en) | 2000-05-19 | 2001-10-02 | The Dow Chemical Company | Carbonate polymer compositions comprising low volatile UV absorbers |
US6828364B2 (en) | 2000-07-14 | 2004-12-07 | Ciba Specialty Chemicals Corporation | Stabilizer mixtures |
JP4488604B2 (ja) | 2000-07-26 | 2010-06-23 | 株式会社Adeka | 難燃性合成樹脂組成物 |
CO5231248A1 (es) | 2000-07-26 | 2002-12-27 | Ciba Sc Holding Ag | Articulos transparentes de polimero de baja consistencia |
US6835329B2 (en) | 2000-10-03 | 2004-12-28 | Ciba Specialty Chemicals Corporation | Heteroaryl substituted hydroxyphenyltriazine uv-absorbers |
US6867250B1 (en) | 2000-10-30 | 2005-03-15 | Cytec Technology Corp. | Non-yellowing ortho-dialkyl aryl substituted triazine ultraviolet light absorbers |
JP3590345B2 (ja) | 2000-11-27 | 2004-11-17 | 三井化学株式会社 | 光記録媒体 |
DE10101222A1 (de) | 2001-01-12 | 2002-07-25 | Agfa Gevaert Ag | Farbfotografisches Silberhalogenidmaterial |
JP4526196B2 (ja) | 2001-02-02 | 2010-08-18 | 大塚化学株式会社 | 紫外線吸収性共重合体、耐候性樹脂組成物及び記録材料 |
BR0207076A (pt) | 2001-02-08 | 2004-01-20 | Ciba Sc Holding Ag | Condicionamento de pigmentos orgânicos |
US6562083B2 (en) | 2001-04-02 | 2003-05-13 | Ciba Specialty Chemicals Corporation | Candle wax stabilized with s-triazines/hals |
JP4146105B2 (ja) | 2001-05-30 | 2008-09-03 | 富士フイルム株式会社 | 紫外線吸収剤及びその製造方法、紫外線吸収剤を含有する組成物、ならびに画像形成方法 |
US6632944B2 (en) | 2001-06-22 | 2003-10-14 | Cytec Technology Corp. | Process for isolation of monophenolic-bisaryl triazines |
TWI318208B (en) | 2001-07-02 | 2009-12-11 | Ciba Sc Holding Ag | Highly compatible hydroxyphenyltriazine uv-absorbers |
US20040198875A1 (en) | 2001-08-15 | 2004-10-07 | Nikolas Kaprinidis | Flame retardant compositions |
US6492533B1 (en) * | 2001-09-18 | 2002-12-10 | Milliken & Company | Bismethine benzodifuranone derivative colorants |
US6800757B2 (en) | 2001-09-27 | 2004-10-05 | Cytec Technology Corp. | Red-shifted triazine ultravioletlight absorbers |
KR20040048959A (ko) | 2001-10-18 | 2004-06-10 | 시바 스페셜티 케미칼스 홀딩 인크. | 유기 물질용 안정화제로서의 나프틸트리아진 |
EP1308308A3 (en) | 2001-10-31 | 2005-08-17 | EASTMAN KODAK COMPANY (a New Jersey corporation) | Ink jet recording element and printing method |
EP1308311A3 (en) | 2001-10-31 | 2005-08-17 | Eastman Kodak Company | Ink jet recording element and printing method |
US6855269B2 (en) | 2001-11-09 | 2005-02-15 | Cytec Technology Corp. | Phenyl ether-substituted hydroxyphenyl triazine ultraviolet light absorbers |
AU2002348236A1 (en) | 2001-12-27 | 2003-07-24 | Cytec Technology Corp. | Uv stabilized thermoplastic olefins |
WO2003070819A1 (en) | 2002-02-19 | 2003-08-28 | Ciba Specialty Chemicals Holding Inc. | Containers or films comprising hydroxyphenlbenzotriazole uv absorbers for protecting contents against the effects of uv radiation |
US6855666B2 (en) | 2002-03-18 | 2005-02-15 | Eastman Kodak Company | Transferable UV protective image overcoat |
AU2003246417A1 (en) | 2002-06-19 | 2004-01-06 | Ciba Specialty Chemicals Holding Inc. | Stabilized polyamide compositions |
EP1308084A1 (en) | 2002-10-02 | 2003-05-07 | Ciba SC Holding AG | Synergistic UV absorber combination |
EP1627011B1 (en) | 2003-05-26 | 2007-12-19 | Ciba SC Holding AG | Highly compatible and non-migratory polymeric uv-absorber |
US7695643B2 (en) | 2005-02-02 | 2010-04-13 | Ciba Specialty Chemicals Corporation | Long wavelength shifted benzotriazole UV-absorbers and their use |
JP5256028B2 (ja) | 2005-06-10 | 2013-08-07 | チバ ホールディング インコーポレーテッド | トリス(ヒドロキシフェニル)トリアジン |
KR101355874B1 (ko) | 2005-06-10 | 2014-02-03 | 시바 홀딩 인크 | 방향족 카보사이클릭 융합된 환 시스템을 갖는하이드록시페닐트리아진 |
US20100119858A1 (en) | 2007-04-25 | 2010-05-13 | Ciba Corporation | Tinted clear coatings for wood |
US8669336B2 (en) | 2008-02-22 | 2014-03-11 | Basf Se | Fluoro levelling agents |
KR101630886B1 (ko) | 2008-05-15 | 2016-06-15 | 바스프 에스이 | 용매계 코팅에 대한 실리콘 무함유 소포제 |
CN102282216B (zh) * | 2009-01-19 | 2014-05-14 | 巴斯夫欧洲公司 | 黑色颜料分散体 |
-
2009
- 2009-12-28 KR KR1020117019406A patent/KR101773621B1/ko active IP Right Grant
- 2009-12-28 ES ES09799114T patent/ES2463674T3/es active Active
- 2009-12-28 JP JP2011545661A patent/JP5675647B2/ja active Active
- 2009-12-28 US US13/144,940 patent/US8691002B2/en active Active
- 2009-12-28 EP EP20090799114 patent/EP2387600B1/en active Active
- 2009-12-28 CN CN200980154692.2A patent/CN102292397B/zh active Active
- 2009-12-28 WO PCT/EP2009/067953 patent/WO2010081625A2/en active Application Filing
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH08510441A (ja) * | 1992-11-25 | 1996-11-05 | ゼネカ・リミテッド | 化合物 |
JP2000504053A (ja) * | 1996-02-01 | 2000-04-04 | ビーエーエスエフ アクチェンゲゼルシャフト | ベンゾジフラノン染料の製造方法 |
JP2002528448A (ja) * | 1998-10-22 | 2002-09-03 | チバ スペシャルティ ケミカルズ ホールディング インコーポレーテッド | オキソベンゾフラニリデン−ジヒドロインドロン類 |
JP2003512996A (ja) * | 1999-11-03 | 2003-04-08 | チバ スペシャルティ ケミカルズ ホールディング インコーポレーテッド | 着色ガラス質材料、それに被覆されているその前駆体ガラス製物品及びその調製方法 |
JP2010534726A (ja) * | 2007-07-19 | 2010-11-11 | ビーエーエスエフ ソシエタス・ヨーロピア | ビス−オキソジヒドロインドリレン−ベンゾジフラノンを含むnir不活性基体 |
Cited By (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2014103628A1 (ja) | 2012-12-27 | 2014-07-03 | 富士フイルム株式会社 | カラーフィルタ用組成物、赤外線透過フィルタ及びその製造方法、並びに赤外線センサー |
US10436959B2 (en) | 2012-12-27 | 2019-10-08 | Fujifilm Corporation | Composition for color filter, infrared transmission filter and production method thereof, and infrared sensor |
WO2014208348A1 (ja) * | 2013-06-24 | 2014-12-31 | 東レ株式会社 | タッチパネル用黒色樹脂組成物 |
JPWO2014208348A1 (ja) * | 2013-06-24 | 2017-02-23 | 東レ株式会社 | タッチパネル用黒色樹脂組成物 |
WO2017158914A1 (ja) | 2016-03-14 | 2017-09-21 | 富士フイルム株式会社 | 組成物、膜、硬化膜、光学センサおよび膜の製造方法 |
WO2019054281A1 (ja) | 2017-09-15 | 2019-03-21 | 富士フイルム株式会社 | 組成物、膜、積層体、赤外線透過フィルタ、固体撮像素子および赤外線センサ |
WO2020049930A1 (ja) | 2018-09-07 | 2020-03-12 | 富士フイルム株式会社 | 車両用ヘッドライトユニット、ヘッドライト用の遮光膜、ヘッドライト用の遮光膜の製造方法 |
WO2020059509A1 (ja) | 2018-09-20 | 2020-03-26 | 富士フイルム株式会社 | 硬化性組成物、硬化膜、赤外線透過フィルタ、積層体、固体撮像素子、センサ、及び、パターン形成方法 |
WO2021039205A1 (ja) | 2019-08-29 | 2021-03-04 | 富士フイルム株式会社 | 組成物、膜、近赤外線カットフィルタ、パターン形成方法、積層体、固体撮像素子、赤外線センサ、画像表示装置、カメラモジュール、及び、化合物 |
WO2022131191A1 (ja) | 2020-12-16 | 2022-06-23 | 富士フイルム株式会社 | 組成物、膜、光学フィルタ、固体撮像素子、画像表示装置および赤外線センサ |
WO2022130773A1 (ja) | 2020-12-17 | 2022-06-23 | 富士フイルム株式会社 | 組成物、膜、光学フィルタ、固体撮像素子、画像表示装置および赤外線センサ |
WO2022210175A1 (ja) | 2021-03-29 | 2022-10-06 | 富士フイルム株式会社 | 黒色感光性組成物、黒色感光性組成物の製造方法、硬化膜、カラーフィルタ、遮光膜、光学素子、固体撮像素子、ヘッドライトユニット |
Also Published As
Publication number | Publication date |
---|---|
CN102292397B (zh) | 2014-12-10 |
US8691002B2 (en) | 2014-04-08 |
CN102292397A (zh) | 2011-12-21 |
KR101773621B1 (ko) | 2017-08-31 |
KR20110108401A (ko) | 2011-10-05 |
JP5675647B2 (ja) | 2015-02-25 |
ES2463674T3 (es) | 2014-05-28 |
WO2010081625A2 (en) | 2010-07-22 |
EP2387600A2 (en) | 2011-11-23 |
US20110294385A1 (en) | 2011-12-01 |
EP2387600B1 (en) | 2014-04-02 |
WO2010081625A3 (en) | 2010-11-04 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JP5675647B2 (ja) | 有機黒色顔料およびその製造 | |
EP0256983B1 (de) | Feste Lösungen von Pyrrolo-[3,4-c]-pyrrolen | |
US7077898B2 (en) | Black pigment compositions | |
US20040249162A1 (en) | Process for the direct preparation of pyrrolo[3 4-c]pyrroles | |
KR100435007B1 (ko) | 1,4-디케토피롤로피롤및퀴나크리돈의3성분고용체 | |
KR960002229B1 (ko) | 피롤로-[3,4-c]-피롤과 퀴나크리돈의 고체 용액 | |
CZ173696A3 (en) | Pigment mixtures prepared from diketopyrrolopyrroles | |
KR101939419B1 (ko) | 표면-개질된 안료 제제 | |
US6869472B2 (en) | 2,9-dichloroquinacridone pigment | |
JP2001187845A (ja) | ジケトピロロピロール | |
EP3197955B1 (en) | Stabilization of c.i. pigment yellow 139 | |
EP3521378B1 (en) | Pyrimidoquinazoline pigment, method for manufacturing pyrimidoquinazoline pigment, and pigment colorant | |
JPH064771B2 (ja) | イソインドリン色素 | |
EP3197954B1 (en) | Pigment composition | |
JP2024502260A (ja) | 近赤外線(nir)透明性中性黒色ペリレン固溶体 | |
AU2002250851A1 (en) | 2, 9-dichloroquinacridone pigment |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
A524 | Written submission of copy of amendment under article 19 pct |
Free format text: JAPANESE INTERMEDIATE CODE: A524 Effective date: 20121225 |
|
A621 | Written request for application examination |
Free format text: JAPANESE INTERMEDIATE CODE: A621 Effective date: 20121225 |
|
A977 | Report on retrieval |
Free format text: JAPANESE INTERMEDIATE CODE: A971007 Effective date: 20140224 |
|
A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20140324 |
|
A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20140618 |
|
TRDD | Decision of grant or rejection written | ||
A01 | Written decision to grant a patent or to grant a registration (utility model) |
Free format text: JAPANESE INTERMEDIATE CODE: A01 Effective date: 20141125 |
|
A61 | First payment of annual fees (during grant procedure) |
Free format text: JAPANESE INTERMEDIATE CODE: A61 Effective date: 20141224 |
|
R150 | Certificate of patent or registration of utility model |
Ref document number: 5675647 Country of ref document: JP Free format text: JAPANESE INTERMEDIATE CODE: R150 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
S111 | Request for change of ownership or part of ownership |
Free format text: JAPANESE INTERMEDIATE CODE: R313113 |
|
R350 | Written notification of registration of transfer |
Free format text: JAPANESE INTERMEDIATE CODE: R350 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |