TW201542526A - 化合物、著色組成物、噴墨記錄用墨水、噴墨記錄方法、噴墨印表機墨水匣及噴墨記錄物 - Google Patents

化合物、著色組成物、噴墨記錄用墨水、噴墨記錄方法、噴墨印表機墨水匣及噴墨記錄物 Download PDF

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Publication number: TW201542526A
Authority: TW; Taiwan
Prior art keywords: group; heterocyclic; formula; aryl; amine
Prior art date: 2014-03-19

Application number

TW104108705A

Other languages

English (en)

Chinese (zh)

Inventor

Shinya Hayashi

Takashi Iizumi

Keiichi Tateishi

Kazushi Furukawa

Original Assignee

Fujifilm Corp

Priority date (The priority date 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 date listed.)

2014-03-19

Filing date

2015-03-19

Publication date

2015-11-16

2015-03-19 Application filed by Fujifilm Corp filed Critical Fujifilm Corp

2015-11-16 Publication of TW201542526A publication Critical patent/TW201542526A/zh

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150000001875 compounds Chemical class 0.000 title claims abstract description 115
239000000203 mixture Substances 0.000 title claims abstract description 65
238000000034 method Methods 0.000 title claims abstract description 41
238000004040 coloring Methods 0.000 title claims abstract description 14
-1 nonyloxy, decyloxy Chemical group 0.000 claims description 228
125000003118 aryl group Chemical group 0.000 claims description 124
125000000217 alkyl group Chemical group 0.000 claims description 115
125000000623 heterocyclic group Chemical group 0.000 claims description 108
125000001424 substituent group Chemical group 0.000 claims description 97
125000004432 carbon atom Chemical group C* 0.000 claims description 90
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 54
125000005843 halogen group Chemical group 0.000 claims description 46
125000003342 alkenyl group Chemical group 0.000 claims description 44
125000004453 alkoxycarbonyl group Chemical group 0.000 claims description 38
125000000304 alkynyl group Chemical group 0.000 claims description 37
125000004390 alkyl sulfonyl group Chemical group 0.000 claims description 35
150000001412 amines Chemical class 0.000 claims description 34
125000005161 aryl oxy carbonyl group Chemical group 0.000 claims description 33
125000004391 aryl sulfonyl group Chemical group 0.000 claims description 33
125000003545 alkoxy group Chemical group 0.000 claims description 29
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 28
125000004093 cyano group Chemical group *C#N 0.000 claims description 27
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 27
125000004104 aryloxy group Chemical group 0.000 claims description 26
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 26
125000003983 fluorenyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3CC12)* 0.000 claims description 25
125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 claims description 25
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125000004466 alkoxycarbonylamino group Chemical group 0.000 claims description 19
125000004656 alkyl sulfonylamino group Chemical group 0.000 claims description 19
125000005110 aryl thio group Chemical group 0.000 claims description 19
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125000005135 aryl sulfinyl group Chemical group 0.000 claims description 18
239000000463 material Substances 0.000 claims description 18
125000005194 alkoxycarbonyloxy group Chemical group 0.000 claims description 17
125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 17
125000005200 aryloxy carbonyloxy group Chemical group 0.000 claims description 16
125000001624 naphthyl group Chemical group 0.000 claims description 16
125000004657 aryl sulfonyl amino group Chemical group 0.000 claims description 14
RSPCKAHMRANGJZ-UHFFFAOYSA-N thiohydroxylamine Chemical compound SN RSPCKAHMRANGJZ-UHFFFAOYSA-N 0.000 claims description 14
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CVXBEEMKQHEXEN-UHFFFAOYSA-N carbaryl Chemical compound C1=CC=C2C(OC(=O)NC)=CC=CC2=C1 CVXBEEMKQHEXEN-UHFFFAOYSA-N 0.000 claims description 6
229960005286 carbaryl Drugs 0.000 claims description 6
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125000003170 phenylsulfonyl group Chemical group C1(=CC=CC=C1)S(=O)(=O)* 0.000 claims description 6
125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 claims description 6
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150000001345 alkine derivatives Chemical class 0.000 claims description 2
BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 claims description 2
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238000003860 storage Methods 0.000 abstract description 15
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125000006615 aromatic heterocyclic group Chemical group 0.000 description 16
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239000003795 chemical substances by application Substances 0.000 description 15
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125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 15
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125000003277 amino group Chemical group 0.000 description 14
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical group C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 13
239000000654 additive Substances 0.000 description 13
239000012736 aqueous medium Substances 0.000 description 13
IAZDPXIOMUYVGZ-WFGJKAKNSA-N Dimethyl sulfoxide Chemical compound [2H]C([2H])([2H])S(=O)C([2H])([2H])[2H] IAZDPXIOMUYVGZ-WFGJKAKNSA-N 0.000 description 12
WMFOQBRAJBCJND-UHFFFAOYSA-M Lithium hydroxide Chemical compound [Li+].[OH-] WMFOQBRAJBCJND-UHFFFAOYSA-M 0.000 description 12
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NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 12
DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 12
125000000751 azo group Chemical group [*]N=N[*] 0.000 description 12
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125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 11
150000002391 heterocyclic compounds Chemical class 0.000 description 11
239000007788 liquid Substances 0.000 description 11
239000003002 pH adjusting agent Substances 0.000 description 11
230000003449 preventive effect Effects 0.000 description 11
239000002585 base Substances 0.000 description 10
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ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 9
125000001309 chloro group Chemical group Cl* 0.000 description 9
230000000694 effects Effects 0.000 description 9
239000002609 medium Substances 0.000 description 9
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VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 8
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239000003112 inhibitor Substances 0.000 description 8
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KWGKDLIKAYFUFQ-UHFFFAOYSA-M lithium chloride Chemical compound [Li+].[Cl-] KWGKDLIKAYFUFQ-UHFFFAOYSA-M 0.000 description 8
239000000126 substance Substances 0.000 description 8
229910052717 sulfur Inorganic materials 0.000 description 8
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159000000002 lithium salts Chemical class 0.000 description 7
125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 7
239000000047 product Substances 0.000 description 7
229910000030 sodium bicarbonate Inorganic materials 0.000 description 7
235000017557 sodium bicarbonate Nutrition 0.000 description 7
125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 7
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HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 6
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229910000147 aluminium phosphate Inorganic materials 0.000 description 6
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238000000354 decomposition reaction Methods 0.000 description 6
DOIRQSBPFJWKBE-UHFFFAOYSA-N dibutyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 description 6
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125000002350 geranyl group Chemical group [H]C([*])([H])/C([H])=C(C([H])([H])[H])/C([H])([H])C([H])([H])C([H])=C(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
229910001385 heavy metal Inorganic materials 0.000 description 1
BRWIZMBXBAOCCF-UHFFFAOYSA-N hydrazinecarbothioamide Chemical compound NNC(N)=S BRWIZMBXBAOCCF-UHFFFAOYSA-N 0.000 description 1
ZMZDMBWJUHKJPS-UHFFFAOYSA-N hydrogen thiocyanate Natural products SC#N ZMZDMBWJUHKJPS-UHFFFAOYSA-N 0.000 description 1
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
238000003384 imaging method Methods 0.000 description 1
150000002460 imidazoles Chemical class 0.000 description 1
229940097275 indigo Drugs 0.000 description 1
COHYTHOBJLSHDF-UHFFFAOYSA-N indigo powder Natural products N1C2=CC=CC=C2C(=O)C1=C1C(=O)C2=CC=CC=C2N1 COHYTHOBJLSHDF-UHFFFAOYSA-N 0.000 description 1
239000004615 ingredient Substances 0.000 description 1
239000013067 intermediate product Substances 0.000 description 1
238000011835 investigation Methods 0.000 description 1
150000002500 ions Chemical class 0.000 description 1
QQVIHTHCMHWDBS-UHFFFAOYSA-L isophthalate(2-) Chemical compound [O-]C(=O)C1=CC=CC(C([O-])=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-L 0.000 description 1
125000003253 isopropoxy group Chemical group [H]C([H])([H])C([H])(O*)C([H])([H])[H] 0.000 description 1
150000002576 ketones Chemical class 0.000 description 1
239000004973 liquid crystal related substance Substances 0.000 description 1
XIXADJRWDQXREU-UHFFFAOYSA-M lithium acetate Chemical compound [Li+].CC([O-])=O XIXADJRWDQXREU-UHFFFAOYSA-M 0.000 description 1
229940031993 lithium benzoate Drugs 0.000 description 1
XGZVUEUWXADBQD-UHFFFAOYSA-L lithium carbonate Chemical compound [Li+].[Li+].[O-]C([O-])=O XGZVUEUWXADBQD-UHFFFAOYSA-L 0.000 description 1
229910052808 lithium carbonate Inorganic materials 0.000 description 1
LDJNSLOKTFFLSL-UHFFFAOYSA-M lithium;benzoate Chemical compound [Li+].[O-]C(=O)C1=CC=CC=C1 LDJNSLOKTFFLSL-UHFFFAOYSA-M 0.000 description 1
230000007774 longterm Effects 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
DZVCFNFOPIZQKX-LTHRDKTGSA-M merocyanine Chemical compound [Na+].O=C1N(CCCC)C(=O)N(CCCC)C(=O)C1=C\C=C\C=C/1N(CCCS([O-])(=O)=O)C2=CC=CC=C2O\1 DZVCFNFOPIZQKX-LTHRDKTGSA-M 0.000 description 1
229940098779 methanesulfonic acid Drugs 0.000 description 1
HNQIVZYLYMDVSB-UHFFFAOYSA-N methanesulfonimidic acid Chemical compound CS(N)(=O)=O HNQIVZYLYMDVSB-UHFFFAOYSA-N 0.000 description 1
125000001434 methanylylidene group Chemical group [H]C#[*] 0.000 description 1
125000000250 methylamino group Chemical group [H]N(*)C([H])([H])[H] 0.000 description 1
125000000325 methylidene group Chemical group [H]C([H])=* 0.000 description 1
125000006216 methylsulfinyl group Chemical group [H]C([H])([H])S(*)=O 0.000 description 1
239000008267 milk Substances 0.000 description 1
210000004080 milk Anatomy 0.000 description 1
235000013336 milk Nutrition 0.000 description 1
150000007522 mineralic acids Chemical class 0.000 description 1
239000003607 modifier Substances 0.000 description 1
235000019796 monopotassium phosphate Nutrition 0.000 description 1
229910000402 monopotassium phosphate Inorganic materials 0.000 description 1
235000019799 monosodium phosphate Nutrition 0.000 description 1
229910000403 monosodium phosphate Inorganic materials 0.000 description 1
125000002757 morpholinyl group Chemical group 0.000 description 1
VMGAPWLDMVPYIA-HIDZBRGKSA-N n'-amino-n-iminomethanimidamide Chemical compound N\N=C\N=N VMGAPWLDMVPYIA-HIDZBRGKSA-N 0.000 description 1
IOKYPACLTOWHCM-UHFFFAOYSA-N n,n-diethyldodecan-1-amine Chemical compound CCCCCCCCCCCCN(CC)CC IOKYPACLTOWHCM-UHFFFAOYSA-N 0.000 description 1
MLQPXAQSJNFRRZ-UHFFFAOYSA-N n-decyldodecan-1-amine Chemical compound CCCCCCCCCCCCNCCCCCCCCCC MLQPXAQSJNFRRZ-UHFFFAOYSA-N 0.000 description 1
125000006608 n-octyloxy group Chemical group 0.000 description 1
150000002790 naphthalenes Chemical class 0.000 description 1
150000004780 naphthols Chemical class 0.000 description 1
150000002791 naphthoquinones Chemical class 0.000 description 1
230000003472 neutralizing effect Effects 0.000 description 1
239000001006 nitroso dye Substances 0.000 description 1
KSCKTBJJRVPGKM-UHFFFAOYSA-N octan-1-olate;titanium(4+) Chemical compound [Ti+4].CCCCCCCC[O-].CCCCCCCC[O-].CCCCCCCC[O-].CCCCCCCC[O-] KSCKTBJJRVPGKM-UHFFFAOYSA-N 0.000 description 1
229920002114 octoxynol-9 Polymers 0.000 description 1
JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
150000002894 organic compounds Chemical class 0.000 description 1
230000003204 osmotic effect Effects 0.000 description 1
150000004893 oxazines Chemical class 0.000 description 1
150000002916 oxazoles Chemical class 0.000 description 1
125000001037 p-tolyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])[H] 0.000 description 1
229940049954 penicillin Drugs 0.000 description 1
229960004321 pentaerithrityl tetranitrate Drugs 0.000 description 1
UWJJYHHHVWZFEP-UHFFFAOYSA-N pentane-1,1-diol Chemical compound CCCCC(O)O UWJJYHHHVWZFEP-UHFFFAOYSA-N 0.000 description 1
125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 1
XQYMIMUDVJCMLU-UHFFFAOYSA-N phenoxyperoxybenzene Chemical class C=1C=CC=CC=1OOOC1=CC=CC=C1 XQYMIMUDVJCMLU-UHFFFAOYSA-N 0.000 description 1
IVDNCEPKBKOMER-UHFFFAOYSA-N phenoxyphosphane Chemical compound POC1=CC=CC=C1 IVDNCEPKBKOMER-UHFFFAOYSA-N 0.000 description 1
CMPQUABWPXYYSH-UHFFFAOYSA-N phenyl phosphate Chemical compound OP(O)(=O)OC1=CC=CC=C1 CMPQUABWPXYYSH-UHFFFAOYSA-N 0.000 description 1
RPGWZZNNEUHDAQ-UHFFFAOYSA-O phenylphosphanium Chemical compound [PH3+]C1=CC=CC=C1 RPGWZZNNEUHDAQ-UHFFFAOYSA-O 0.000 description 1
235000021317 phosphate Nutrition 0.000 description 1
125000005499 phosphonyl group Chemical group 0.000 description 1
PJNZPQUBCPKICU-UHFFFAOYSA-N phosphoric acid;potassium Chemical compound [K].OP(O)(O)=O PJNZPQUBCPKICU-UHFFFAOYSA-N 0.000 description 1
229910000073 phosphorus hydride Inorganic materials 0.000 description 1
ZFACJPAPCXRZMQ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O.OC(=O)C1=CC=CC=C1C(O)=O ZFACJPAPCXRZMQ-UHFFFAOYSA-N 0.000 description 1
150000003021 phthalic acid derivatives Chemical class 0.000 description 1
229940081066 picolinic acid Drugs 0.000 description 1
239000002985 plastic film Substances 0.000 description 1
229920006255 plastic film Polymers 0.000 description 1
239000002861 polymer material Substances 0.000 description 1
235000011056 potassium acetate Nutrition 0.000 description 1
CHKVPAROMQMJNQ-UHFFFAOYSA-M potassium bisulfate Chemical compound [K+].OS([O-])(=O)=O CHKVPAROMQMJNQ-UHFFFAOYSA-M 0.000 description 1
229910000343 potassium bisulfate Inorganic materials 0.000 description 1
229910000027 potassium carbonate Inorganic materials 0.000 description 1
235000011181 potassium carbonates Nutrition 0.000 description 1
CASUWPDYGGAUQV-UHFFFAOYSA-M potassium;methanol;hydroxide Chemical compound [OH-].[K+].OC CASUWPDYGGAUQV-UHFFFAOYSA-M 0.000 description 1
125000001844 prenyl group Chemical group [H]C([*])([H])C([H])=C(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
238000011085 pressure filtration Methods 0.000 description 1
JEXVQSWXXUJEMA-UHFFFAOYSA-N pyrazol-3-one Chemical class O=C1C=CN=N1 JEXVQSWXXUJEMA-UHFFFAOYSA-N 0.000 description 1
150000003222 pyridines Chemical class 0.000 description 1
125000001453 quaternary ammonium group Chemical group 0.000 description 1
150000003242 quaternary ammonium salts Chemical class 0.000 description 1
IZMJMCDDWKSTTK-UHFFFAOYSA-N quinoline yellow Chemical compound C1=CC=CC2=NC(C3C(C4=CC=CC=C4C3=O)=O)=CC=C21 IZMJMCDDWKSTTK-UHFFFAOYSA-N 0.000 description 1
GJAWHXHKYYXBSV-UHFFFAOYSA-N quinolinic acid Chemical compound OC(=O)C1=CC=CN=C1C(O)=O GJAWHXHKYYXBSV-UHFFFAOYSA-N 0.000 description 1
230000005855 radiation Effects 0.000 description 1
239000002994 raw material Substances 0.000 description 1
238000010992 reflux Methods 0.000 description 1
BOLDJAUMGUJJKM-LSDHHAIUSA-N renifolin D Natural products CC(=C)[C@@H]1Cc2c(O)c(O)ccc2[C@H]1CC(=O)c3ccc(O)cc3O BOLDJAUMGUJJKM-LSDHHAIUSA-N 0.000 description 1
238000011160 research Methods 0.000 description 1
238000000926 separation method Methods 0.000 description 1
238000010008 shearing Methods 0.000 description 1
238000004513 sizing Methods 0.000 description 1
235000015424 sodium Nutrition 0.000 description 1
239000001632 sodium acetate Substances 0.000 description 1
235000017281 sodium acetate Nutrition 0.000 description 1
229960003885 sodium benzoate Drugs 0.000 description 1
WBHQBSYUUJJSRZ-UHFFFAOYSA-M sodium bisulfate Chemical compound [Na+].OS([O-])(=O)=O WBHQBSYUUJJSRZ-UHFFFAOYSA-M 0.000 description 1
229910000342 sodium bisulfate Inorganic materials 0.000 description 1
229910000029 sodium carbonate Inorganic materials 0.000 description 1
235000002639 sodium chloride Nutrition 0.000 description 1
AJPJDKMHJJGVTQ-UHFFFAOYSA-M sodium dihydrogen phosphate Chemical compound [Na+].OP(O)([O-])=O AJPJDKMHJJGVTQ-UHFFFAOYSA-M 0.000 description 1
239000004402 sodium ethyl p-hydroxybenzoate Substances 0.000 description 1
235000010226 sodium ethyl p-hydroxybenzoate Nutrition 0.000 description 1
239000001488 sodium phosphate Substances 0.000 description 1
229910000162 sodium phosphate Inorganic materials 0.000 description 1
235000011008 sodium phosphates Nutrition 0.000 description 1
AKHNMLFCWUSKQB-UHFFFAOYSA-L sodium thiosulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=S AKHNMLFCWUSKQB-UHFFFAOYSA-L 0.000 description 1
235000019345 sodium thiosulphate Nutrition 0.000 description 1
238000013112 stability test Methods 0.000 description 1
150000003431 steroids Chemical class 0.000 description 1
125000003107 substituted aryl group Chemical group 0.000 description 1
125000000626 sulfinic acid group Chemical group 0.000 description 1
150000003456 sulfonamides Chemical class 0.000 description 1
125000006296 sulfonyl amino group Chemical group [H]N(*)S(*)(=O)=O 0.000 description 1
238000001308 synthesis method Methods 0.000 description 1
230000002194 synthesizing effect Effects 0.000 description 1
235000002906 tartaric acid Nutrition 0.000 description 1
239000011975 tartaric acid Substances 0.000 description 1
238000012360 testing method Methods 0.000 description 1
235000019364 tetracycline Nutrition 0.000 description 1
229960002180 tetracycline Drugs 0.000 description 1
229930101283 tetracycline Natural products 0.000 description 1
150000003522 tetracyclines Chemical class 0.000 description 1
QEMXHQIAXOOASZ-UHFFFAOYSA-N tetramethylammonium Chemical compound C[N+](C)(C)C QEMXHQIAXOOASZ-UHFFFAOYSA-N 0.000 description 1
150000008334 thiadiazines Chemical class 0.000 description 1
150000003557 thiazoles Chemical class 0.000 description 1
125000005300 thiocarboxy group Chemical group C(=S)(O)* 0.000 description 1
150000003568 thioethers Chemical class 0.000 description 1
150000003585 thioureas Chemical class 0.000 description 1
150000003918 triazines Chemical class 0.000 description 1
125000001425 triazolyl group Chemical group 0.000 description 1
RJIFVNWOLLIBJV-UHFFFAOYSA-N tributyl benzene-1,2,4-tricarboxylate Chemical compound CCCCOC(=O)C1=CC=C(C(=O)OCCCC)C(C(=O)OCCCC)=C1 RJIFVNWOLLIBJV-UHFFFAOYSA-N 0.000 description 1
IELLVVGAXDLVSW-UHFFFAOYSA-N tricyclohexyl phosphate Chemical compound C1CCCCC1OP(OC1CCCCC1)(=O)OC1CCCCC1 IELLVVGAXDLVSW-UHFFFAOYSA-N 0.000 description 1
OHRVKCZTBPSUIK-UHFFFAOYSA-N tridodecyl phosphate Chemical compound CCCCCCCCCCCCOP(=O)(OCCCCCCCCCCCC)OCCCCCCCCCCCC OHRVKCZTBPSUIK-UHFFFAOYSA-N 0.000 description 1
150000003639 trimesic acids Chemical class 0.000 description 1
APVVRLGIFCYZHJ-UHFFFAOYSA-N trioctyl 2-hydroxypropane-1,2,3-tricarboxylate Chemical compound CCCCCCCCOC(=O)CC(O)(C(=O)OCCCCCCCC)CC(=O)OCCCCCCCC APVVRLGIFCYZHJ-UHFFFAOYSA-N 0.000 description 1
XZZNDPSIHUTMOC-UHFFFAOYSA-N triphenyl phosphate Chemical compound C=1C=CC=CC=1OP(OC=1C=CC=CC=1)(=O)OC1=CC=CC=C1 XZZNDPSIHUTMOC-UHFFFAOYSA-N 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
RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 description 1
238000003828 vacuum filtration Methods 0.000 description 1
238000005406 washing Methods 0.000 description 1
239000001018 xanthene dye 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
125000002256 xylenyl group Chemical class C1(C(C=CC=C1)C)(C)* 0.000 description 1
239000001052 yellow pigment Substances 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D11/00—Inks
- C09D11/30—Inkjet printing inks
- C09D11/32—Inkjet printing inks characterised by colouring agents
- C09D11/322—Pigment inks
- 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
- C09B31/00—Disazo and polyazo dyes of the type A->B->C, A->B->C->D, or the like, prepared by diazotising and coupling
- C09B31/02—Disazo dyes
- C09B31/12—Disazo dyes from other coupling components "C"
- C09B31/14—Heterocyclic components
- C09B31/153—Heterocyclic components containing a six-membered ring with one nitrogen atom as the only ring hetero-atom

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Life Sciences & Earth Sciences (AREA)
Engineering & Computer Science (AREA)
Materials Engineering (AREA)
Wood Science & Technology (AREA)
Inks, Pencil-Leads, Or Crayons (AREA)
Ink Jet Recording Methods And Recording Media Thereof (AREA)
Pigments, Carbon Blacks, Or Wood Stains (AREA)
Ink Jet (AREA)

TW104108705A 2014-03-19 2015-03-19 化合物、著色組成物、噴墨記錄用墨水、噴墨記錄方法、噴墨印表機墨水匣及噴墨記錄物 TW201542526A (zh)

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JP (1)	JP2015178576A (fr)
TW (1)	TW201542526A (fr)
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JP6247971B2 (ja) *	2014-03-19	2017-12-13	富士フイルム株式会社	化合物、着色組成物、インクジェット記録用インク、インクジェット記録方法、インクジェットプリンタカートリッジ、及びインクジェット記録物
JP2023125501A (ja) *	2022-02-28	2023-09-07	ブラザー工業株式会社	インクジェット記録用水性インク、インクジェット記録方法、インクジェット記録装置、及びインク収容容器

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JPS5246230B2 (fr) *	1972-12-16	1977-11-22
IT985617B (it) *	1972-04-06	1974-12-10	Basf Ag	Azocoloranti idrosolubili della serie 2 6 diamminopiridinica
DE2230392A1 (de) *	1972-06-22	1974-01-31	Cassella Farbwerke Mainkur Ag	Substituierte pyridinverbindungen und verfahren zu ihrer herstellung
JP3222236B2 (ja) *	1993-01-11	2001-10-22	三井化学株式会社	感熱昇華転写記録用マゼンタ系色素、同色素を含むインキ組成物、及び転写シート
DE19706245A1 (de) *	1997-02-18	1998-08-20	Basf Ag	Trifluormethylsubstituierte Azofarbstoffe
JP2003206230A (ja) *	2002-01-10	2003-07-22	Yamanouchi Pharmaceut Co Ltd	シアノヘテロ環誘導体又はその塩
WO2004005472A2 (fr) *	2002-07-02	2004-01-15	Southern Research Institute	Inhibiteurs de ftsz et leurs utilisations
JP2004067898A (ja) *	2002-08-07	2004-03-04	Fuji Photo Film Co Ltd	着色組成物、インクジェット記録用インク及びインクジェット記録方法
JP4383156B2 (ja) *	2003-01-08	2009-12-16	富士フイルム株式会社	インクジェット用インク、インクジェット記録方法およびカラートナー用組成物
WO2006034473A2 (fr) *	2004-09-23	2006-03-30	Reddy Us Therapeutics, Inc.	Nouveaux composes de pyrimidine, leur procede de preparation, et compositions les contenant
JP2007099825A (ja) *	2005-09-30	2007-04-19	Fujifilm Corp	水性インク、インクジェット記録用インク、インクジェット記録方法、記録物、インクカートリッジ、インクジェットプリンタ
WO2008053812A1 (fr) *	2006-10-27	2008-05-08	Mitsubishi Tanabe Pharma Corporation	Dérivé de cyanopyridine et son utilisation médicale
MX2010008700A (es) *	2008-02-22	2010-08-30	Hoffmann La Roche	Moduladores de beta-amiloide.
JP5866150B2 (ja) *	2010-07-30	2016-02-17	富士フイルム株式会社	新規なアゾ化合物、水溶液、インク組成物、インクジェット記録用インク、インクジェット記録方法、インクジェット記録用インクカートリッジ、及びインクジェット記録物
CA2870095A1 (fr) *	2012-04-30	2013-11-07	Scifluor Life Sciences, Llc	Derives fluores de 2-amino-4-(benzylamino)phenylcarbamate

2014
- 2014-03-19 JP JP2014057180A patent/JP2015178576A/ja not_active Abandoned
- 2014-12-24 WO PCT/JP2014/084091 patent/WO2015141095A1/fr not_active Ceased
2015
- 2015-03-19 TW TW104108705A patent/TW201542526A/zh unknown

Also Published As

Publication number	Publication date
WO2015141095A1 (fr)	2015-09-24
JP2015178576A (ja)	2015-10-08

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