TWI635326B

TWI635326B - 紅色著色硬化性樹脂組合物

紅色著色硬化性樹脂組合物 Download PDF

Info

Publication number: TWI635326B
Authority: TW; Taiwan
Prior art keywords: group; hydrocarbon group; carbon atoms; pigment; formula
Prior art date: 2011-12-09

Application number

TW101146261A

Other languages

English (en)

Chinese (zh)

Other versions

TW201331712A (zh

Inventor

Soyeon Park

朴昭妍

Original Assignee

Sumitomo Chemical Co., Ltd.

住友化學股份有限公司

Dongwoo Fine-Chem Co., Ltd.

東友精細化工有限公司

Priority date

2011-12-09

Filing date

2012-12-07

Publication date

2018-09-11

2012-12-07 Application filed by Sumitomo Chemical Co., Ltd., 住友化學股份有限公司, Dongwoo Fine-Chem Co., Ltd., 東友精細化工有限公司 filed Critical Sumitomo Chemical Co., Ltd.

2013-08-01 Publication of TW201331712A publication Critical patent/TW201331712A/zh

2018-09-11 Application granted granted Critical

2018-09-11 Publication of TWI635326B publication Critical patent/TWI635326B/zh

Links

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239000011347 resin Substances 0.000 claims abstract description 81
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125000004432 carbon atom Chemical group C* 0.000 claims abstract description 69
239000000049 pigment Substances 0.000 claims abstract description 55
229930195734 saturated hydrocarbon Natural products 0.000 claims abstract description 36
125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract description 33
239000003505 polymerization initiator Substances 0.000 claims abstract description 33
125000002029 aromatic hydrocarbon group Chemical group 0.000 claims abstract description 24
125000000217 alkyl group Chemical group 0.000 claims abstract description 21
239000003086 colorant Substances 0.000 claims abstract description 15
125000001424 substituent group Chemical group 0.000 claims abstract description 14
125000005843 halogen group Chemical group 0.000 claims abstract description 13
239000001053 orange pigment Substances 0.000 claims abstract description 5
239000001054 red pigment Substances 0.000 claims abstract description 5
239000001052 yellow pigment Substances 0.000 claims abstract description 5
125000001183 hydrocarbyl group Chemical group 0.000 claims abstract 10
229910052757 nitrogen Inorganic materials 0.000 claims description 40
125000004433 nitrogen atom Chemical group N* 0.000 claims description 32
229910052799 carbon Inorganic materials 0.000 claims description 8
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239000011734 sodium Substances 0.000 description 5
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125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 1
WLVPQQDEYVVXJF-UHFFFAOYSA-N phenyl bicyclo[2.2.1]hept-2-ene-5-carboxylate Chemical compound C1C(C=C2)CC2C1C(=O)OC1=CC=CC=C1 WLVPQQDEYVVXJF-UHFFFAOYSA-N 0.000 description 1
HPAFOABSQZMTHE-UHFFFAOYSA-N phenyl-(2,4,6-trimethylphenyl)methanone Chemical compound CC1=CC(C)=CC(C)=C1C(=O)C1=CC=CC=C1 HPAFOABSQZMTHE-UHFFFAOYSA-N 0.000 description 1
LYXOWKPVTCPORE-UHFFFAOYSA-N phenyl-(4-phenylphenyl)methanone Chemical compound C=1C=C(C=2C=CC=CC=2)C=CC=1C(=O)C1=CC=CC=C1 LYXOWKPVTCPORE-UHFFFAOYSA-N 0.000 description 1
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XNGIFLGASWRNHJ-UHFFFAOYSA-L phthalate(2-) Chemical compound [O-]C(=O)C1=CC=CC=C1C([O-])=O XNGIFLGASWRNHJ-UHFFFAOYSA-L 0.000 description 1
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BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
125000002572 propoxy group Chemical group [*]OC([H])([H])C(C([H])([H])[H])([H])[H] 0.000 description 1
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ILPVOWZUBFRIAX-UHFFFAOYSA-N propyl 2-oxopropanoate Chemical compound CCCOC(=O)C(C)=O ILPVOWZUBFRIAX-UHFFFAOYSA-N 0.000 description 1
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DHHGSXPASZBLGC-VPMNAVQSSA-L remazole orange-3R Chemical compound [Na+].[Na+].OC=1C2=CC(NC(=O)C)=CC=C2C=C(S([O-])(=O)=O)C=1\N=N\C1=CC=C(S(=O)(=O)CCOS([O-])(=O)=O)C=C1 DHHGSXPASZBLGC-VPMNAVQSSA-L 0.000 description 1
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AXMCIYLNKNGNOT-UHFFFAOYSA-M sodium;3-[[4-[(4-dimethylazaniumylidenecyclohexa-2,5-dien-1-ylidene)-[4-[ethyl-[(3-sulfonatophenyl)methyl]amino]phenyl]methyl]-n-ethylanilino]methyl]benzenesulfonate Chemical compound [Na+].C=1C=C(C(=C2C=CC(C=C2)=[N+](C)C)C=2C=CC(=CC=2)N(CC)CC=2C=C(C=CC=2)S([O-])(=O)=O)C=CC=1N(CC)CC1=CC=CC(S([O-])(=O)=O)=C1 AXMCIYLNKNGNOT-UHFFFAOYSA-M 0.000 description 1
STZCRXQWRGQSJD-UHFFFAOYSA-N sodium;4-[[4-(dimethylamino)phenyl]diazenyl]benzenesulfonic acid Chemical compound [Na+].C1=CC(N(C)C)=CC=C1N=NC1=CC=C(S(O)(=O)=O)C=C1 STZCRXQWRGQSJD-UHFFFAOYSA-N 0.000 description 1
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MUTNCGKQJGXKEM-UHFFFAOYSA-N tamibarotene Chemical compound C=1C=C2C(C)(C)CCC(C)(C)C2=CC=1NC(=O)C1=CC=C(C(O)=O)C=C1 MUTNCGKQJGXKEM-UHFFFAOYSA-N 0.000 description 1
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ISXSCDLOGDJUNJ-UHFFFAOYSA-N tert-butyl prop-2-enoate Chemical class CC(C)(C)OC(=O)C=C ISXSCDLOGDJUNJ-UHFFFAOYSA-N 0.000 description 1
125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 1
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238000004448 titration Methods 0.000 description 1
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 1
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125000003258 trimethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])[*:1] 0.000 description 1
AAAQKTZKLRYKHR-UHFFFAOYSA-N triphenylmethane Chemical compound C1=CC=CC=C1C(C=1C=CC=CC=1)C1=CC=CC=C1 AAAQKTZKLRYKHR-UHFFFAOYSA-N 0.000 description 1
UJMBCXLDXJUMFB-UHFFFAOYSA-K trisodium;5-oxo-1-(4-sulfonatophenyl)-4-[(4-sulfonatophenyl)diazenyl]-4h-pyrazole-3-carboxylate Chemical compound [Na+].[Na+].[Na+].[O-]C(=O)C1=NN(C=2C=CC(=CC=2)S([O-])(=O)=O)C(=O)C1N=NC1=CC=C(S([O-])(=O)=O)C=C1 UJMBCXLDXJUMFB-UHFFFAOYSA-K 0.000 description 1
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