JPS6317102B2 - - Google Patents

Info

Publication number: JPS6317102B2
Authority: JP; Japan
Prior art keywords: pigment; pigments; azo; production example; general formula
Prior art date: 1979-10-26
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.): Expired

Application number

JP13770779A

Other languages

English (en)

Japanese (ja)

Other versions

JPS5661461A (en

Inventor

Shigeyuki Ehashi

Hiromitsu Katsura

Kenichi Kakimoto

Junichi Tsuchida

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Artience Co Ltd

Original Assignee

Toyo Ink Mfg Co Ltd

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.)

1979-10-26

Filing date

1979-10-26

Publication date

1988-04-12

1979-10-26 Application filed by Toyo Ink Mfg Co Ltd filed Critical Toyo Ink Mfg Co Ltd

1979-10-26 Priority to JP13770779A priority Critical patent/JPS5661461A/ja

1981-05-26 Publication of JPS5661461A publication Critical patent/JPS5661461A/ja

1988-04-12 Publication of JPS6317102B2 publication Critical patent/JPS6317102B2/ja

Status Granted legal-status Critical Current

Links

239000000049 pigment Substances 0.000 claims description 60
239000000203 mixture Substances 0.000 claims description 17
239000000987 azo dye Substances 0.000 claims description 15
-1 azo compound Chemical class 0.000 claims description 14
125000000217 alkyl group Chemical group 0.000 claims description 5
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 4
125000004432 carbon atom Chemical group C* 0.000 claims description 4
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 3
229910052757 nitrogen Inorganic materials 0.000 claims description 3
125000000623 heterocyclic group Chemical group 0.000 claims description 2
125000004430 oxygen atom Chemical group O* 0.000 claims description 2
239000003973 paint Substances 0.000 description 29
238000004519 manufacturing process Methods 0.000 description 27
150000001875 compounds Chemical class 0.000 description 19
239000000976 ink Substances 0.000 description 15
238000010992 reflux Methods 0.000 description 13
239000002966 varnish Substances 0.000 description 12
238000000034 method Methods 0.000 description 11
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 9
238000002156 mixing Methods 0.000 description 9
230000000052 comparative effect Effects 0.000 description 8
238000007796 conventional method Methods 0.000 description 8
230000008878 coupling Effects 0.000 description 8
238000010168 coupling process Methods 0.000 description 8
238000005859 coupling reaction Methods 0.000 description 8
FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 description 8
150000001412 amines Chemical class 0.000 description 7
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 6
125000000751 azo group Chemical group [*]N=N[*] 0.000 description 6
239000013078 crystal Substances 0.000 description 6
125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 description 6
239000006185 dispersion Substances 0.000 description 6
230000000694 effects Effects 0.000 description 6
239000002687 nonaqueous vehicle Substances 0.000 description 6
239000008096 xylene Substances 0.000 description 6
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
238000004220 aggregation Methods 0.000 description 4
230000002776 aggregation Effects 0.000 description 4
235000019646 color tone Nutrition 0.000 description 4
238000004040 coloring Methods 0.000 description 4
239000000975 dye Substances 0.000 description 4
239000012860 organic pigment Substances 0.000 description 4
239000000843 powder Substances 0.000 description 4
229920005989 resin Polymers 0.000 description 4
239000011347 resin Substances 0.000 description 4
NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical compound CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 description 3
239000000020 Nitrocellulose Substances 0.000 description 3
GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 3
229910052784 alkaline earth metal Inorganic materials 0.000 description 3
239000011248 coating agent Substances 0.000 description 3
238000000576 coating method Methods 0.000 description 3
239000010419 fine particle Substances 0.000 description 3
239000001023 inorganic pigment Substances 0.000 description 3
239000004922 lacquer Substances 0.000 description 3
229920001220 nitrocellulos Polymers 0.000 description 3
230000002829 reductive effect Effects 0.000 description 3
238000000926 separation method Methods 0.000 description 3
239000002904 solvent Substances 0.000 description 3
238000003860 storage Methods 0.000 description 3
125000001424 substituent group Chemical group 0.000 description 3
OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 3
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical class [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 description 2
JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 2
NRCMAYZCPIVABH-UHFFFAOYSA-N Quinacridone Chemical compound N1C2=CC=CC=C2C(=O)C2=C1C=C1C(=O)C3=CC=CC=C3NC1=C2 NRCMAYZCPIVABH-UHFFFAOYSA-N 0.000 description 2
QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 2
229910052782 aluminium Inorganic materials 0.000 description 2
XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
150000004982 aromatic amines Chemical class 0.000 description 2
150000001732 carboxylic acid derivatives Chemical class 0.000 description 2
150000004985 diamines Chemical class 0.000 description 2
WASQWSOJHCZDFK-UHFFFAOYSA-N diketene Chemical compound C=C1CC(=O)O1 WASQWSOJHCZDFK-UHFFFAOYSA-N 0.000 description 2
238000010438 heat treatment Methods 0.000 description 2
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 2
125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 2
238000003756 stirring Methods 0.000 description 2
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
KNDAEDDIIQYRHY-UHFFFAOYSA-N 2-[4-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]-3-(piperazin-1-ylmethyl)pyrazol-1-yl]-1-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)ethanone Chemical group C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)C=1C(=NN(C=1)CC(=O)N1CC2=C(CC1)NN=N2)CN1CCNCC1 KNDAEDDIIQYRHY-UHFFFAOYSA-N 0.000 description 1
ALKYHXVLJMQRLQ-UHFFFAOYSA-N 3-Hydroxy-2-naphthoate Chemical compound C1=CC=C2C=C(O)C(C(=O)O)=CC2=C1 ALKYHXVLJMQRLQ-UHFFFAOYSA-N 0.000 description 1
SKDHHIUENRGTHK-UHFFFAOYSA-N 4-nitrobenzoyl chloride Chemical compound [O-][N+](=O)C1=CC=C(C(Cl)=O)C=C1 SKDHHIUENRGTHK-UHFFFAOYSA-N 0.000 description 1
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 1
239000004923 Acrylic lacquer Substances 0.000 description 1
239000004925 Acrylic resin Substances 0.000 description 1
229920000178 Acrylic resin Polymers 0.000 description 1
VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
235000008733 Citrus aurantifolia Nutrition 0.000 description 1
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 1
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 1
RAHZWNYVWXNFOC-UHFFFAOYSA-N Sulphur dioxide Chemical group O=S=O RAHZWNYVWXNFOC-UHFFFAOYSA-N 0.000 description 1
235000011941 Tilia x europaea Nutrition 0.000 description 1
XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 1
DYRDKSSFIWVSNM-UHFFFAOYSA-N acetoacetanilide Chemical class CC(=O)CC(=O)NC1=CC=CC=C1 DYRDKSSFIWVSNM-UHFFFAOYSA-N 0.000 description 1
239000002253 acid Substances 0.000 description 1
238000007605 air drying Methods 0.000 description 1
229920000180 alkyd Polymers 0.000 description 1
125000004202 aminomethyl group Chemical group [H]N([H])C([H])([H])* 0.000 description 1
229940051880 analgesics and antipyretics pyrazolones Drugs 0.000 description 1
IRERQBUNZFJFGC-UHFFFAOYSA-L azure blue Chemical compound [Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Al+3].[Al+3].[Al+3].[Al+3].[Al+3].[Al+3].[S-]S[S-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-] IRERQBUNZFJFGC-UHFFFAOYSA-L 0.000 description 1
239000000981 basic dye Substances 0.000 description 1
230000003796 beauty Effects 0.000 description 1
150000001555 benzenes Chemical class 0.000 description 1
238000009835 boiling Methods 0.000 description 1
229910052793 cadmium Inorganic materials 0.000 description 1
BDOSMKKIYDKNTQ-UHFFFAOYSA-N cadmium atom Chemical compound [Cd] BDOSMKKIYDKNTQ-UHFFFAOYSA-N 0.000 description 1
CJOBVZJTOIVNNF-UHFFFAOYSA-N cadmium sulfide Chemical compound [Cd]=S CJOBVZJTOIVNNF-UHFFFAOYSA-N 0.000 description 1
239000006229 carbon black Substances 0.000 description 1
238000006243 chemical reaction Methods 0.000 description 1
229910001919 chlorite Inorganic materials 0.000 description 1
229910052619 chlorite group Inorganic materials 0.000 description 1
XTHPWXDJESJLNJ-UHFFFAOYSA-N chlorosulfonic acid Substances OS(Cl)(=O)=O XTHPWXDJESJLNJ-UHFFFAOYSA-N 0.000 description 1
QBWCMBCROVPCKQ-UHFFFAOYSA-N chlorous acid Chemical compound OCl=O QBWCMBCROVPCKQ-UHFFFAOYSA-N 0.000 description 1
239000011362 coarse particle Substances 0.000 description 1
239000008199 coating composition Substances 0.000 description 1
238000009500 colour coating Methods 0.000 description 1
238000005520 cutting process Methods 0.000 description 1
238000000354 decomposition reaction Methods 0.000 description 1
238000007033 dehydrochlorination reaction Methods 0.000 description 1
PPSZHCXTGRHULJ-UHFFFAOYSA-N dioxazine Chemical compound O1ON=CC=C1 PPSZHCXTGRHULJ-UHFFFAOYSA-N 0.000 description 1
230000002349 favourable effect Effects 0.000 description 1
235000013305 food Nutrition 0.000 description 1
238000001879 gelation Methods 0.000 description 1
239000011521 glass Substances 0.000 description 1
125000005843 halogen group Chemical group 0.000 description 1
RBTKNAXYKSUFRK-UHFFFAOYSA-N heliogen blue Chemical compound [Cu].[N-]1C2=C(C=CC=C3)C3=C1N=C([N-]1)C3=CC=CC=C3C1=NC([N-]1)=C(C=CC=C3)C3=C1N=C([N-]1)C3=CC=CC=C3C1=N2 RBTKNAXYKSUFRK-UHFFFAOYSA-N 0.000 description 1
UCNNJGDEJXIUCC-UHFFFAOYSA-L hydroxy(oxo)iron;iron Chemical compound [Fe].O[Fe]=O.O[Fe]=O UCNNJGDEJXIUCC-UHFFFAOYSA-L 0.000 description 1
239000005457 ice water Substances 0.000 description 1
230000001771 impaired effect Effects 0.000 description 1
PXZQEOJJUGGUIB-UHFFFAOYSA-N isoindolin-1-one Chemical compound C1=CC=C2C(=O)NCC2=C1 PXZQEOJJUGGUIB-UHFFFAOYSA-N 0.000 description 1
239000004571 lime Substances 0.000 description 1
239000000463 material Substances 0.000 description 1
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
QOHMWDJIBGVPIF-UHFFFAOYSA-N n',n'-diethylpropane-1,3-diamine Chemical compound CCN(CC)CCCN QOHMWDJIBGVPIF-UHFFFAOYSA-N 0.000 description 1
YPLIFKZBNCNJJN-UHFFFAOYSA-N n,n-bis(ethylamino)ethanamine Chemical compound CCNN(CC)NCC YPLIFKZBNCNJJN-UHFFFAOYSA-N 0.000 description 1
150000002790 naphthalenes Chemical class 0.000 description 1
150000004780 naphthols Chemical class 0.000 description 1
239000003960 organic solvent Substances 0.000 description 1
230000000242 pagocytic effect Effects 0.000 description 1
239000002245 particle Substances 0.000 description 1
125000002080 perylenyl group Chemical group C1(=CC=C2C=CC=C3C4=CC=CC5=CC=CC(C1=C23)=C45)* 0.000 description 1
CSHWQDPOILHKBI-UHFFFAOYSA-N peryrene Natural products C1=CC(C2=CC=CC=3C2=C2C=CC=3)=C3C2=CC=CC3=C1 CSHWQDPOILHKBI-UHFFFAOYSA-N 0.000 description 1
150000002989 phenols Chemical class 0.000 description 1
IEQIEDJGQAUEQZ-UHFFFAOYSA-N phthalocyanine Chemical compound N1C(N=C2C3=CC=CC=C3C(N=C3C4=CC=CC=C4C(=N4)N3)=N2)=C(C=CC=C2)C2=C1N=C1C2=CC=CC=C2C4=N1 IEQIEDJGQAUEQZ-UHFFFAOYSA-N 0.000 description 1
229920006122 polyamide resin Polymers 0.000 description 1
238000002360 preparation method Methods 0.000 description 1
JEXVQSWXXUJEMA-UHFFFAOYSA-N pyrazol-3-one Chemical class O=C1C=CN=N1 JEXVQSWXXUJEMA-UHFFFAOYSA-N 0.000 description 1
239000002994 raw material Substances 0.000 description 1
238000004062 sedimentation Methods 0.000 description 1
239000002002 slurry Substances 0.000 description 1
239000000126 substance Substances 0.000 description 1
229940124530 sulfonamide Drugs 0.000 description 1
125000000565 sulfonamide group Chemical group 0.000 description 1
150000003456 sulfonamides Chemical class 0.000 description 1
125000001174 sulfone group Chemical group 0.000 description 1
YBBRCQOCSYXUOC-UHFFFAOYSA-N sulfuryl dichloride Chemical group ClS(Cl)(=O)=O YBBRCQOCSYXUOC-UHFFFAOYSA-N 0.000 description 1
239000000725 suspension Substances 0.000 description 1
238000001308 synthesis method Methods 0.000 description 1
229920002803 thermoplastic polyurethane Polymers 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
235000013799 ultramarine blue Nutrition 0.000 description 1
239000000984 vat dye Substances 0.000 description 1
239000003981 vehicle Substances 0.000 description 1
238000005406 washing Methods 0.000 description 1
235000014692 zinc oxide Nutrition 0.000 description 1
239000011787 zinc oxide Substances 0.000 description 1

Landscapes

Inks, Pencil-Leads, Or Crayons (AREA)
Compositions Of Macromolecular Compounds (AREA)

JP13770779A 1979-10-26 1979-10-26 Pigment composition Granted JPS5661461A (en)

Priority Applications (1)

Application Number	Priority Date	Filing Date	Title
JP13770779A JPS5661461A (en)	1979-10-26	1979-10-26	Pigment composition

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
JP13770779A JPS5661461A (en)	1979-10-26	1979-10-26	Pigment composition

Publications (2)

Publication Number	Publication Date
JPS5661461A JPS5661461A (en)	1981-05-26
JPS6317102B2 true JPS6317102B2 (ko)	1988-04-12

Family

ID=15204935

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP13770779A Granted JPS5661461A (en)	1979-10-26	1979-10-26	Pigment composition

Country Status (1)

Country	Link
JP (1)	JPS5661461A (ko)

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
EP1676889A1 (en)	2004-12-03	2006-07-05	Toyo Ink Mfg. Co., Ltd.	Colored composition
WO2008099879A1 (ja)	2007-02-16	2008-08-21	Toppan Printing Co., Ltd.	リターデイション基板、その製造方法及び液晶表示装置
WO2009122621A1 (ja)	2008-03-31	2009-10-08	凸版印刷株式会社	位相差板、その製造方法及び液晶表示装置
US8665404B2 (en)	2007-12-21	2014-03-04	Nitto Denko Corporation	Liquid crystal cell substrate, liquid crystal cell, liquid crystal panel, and liquid crystal display
WO2014061747A1 (ja)	2012-10-17	2014-04-24	東洋インキＳｃホールディングス株式会社	液体現像剤用高分子分散剤、液体現像剤、及び印刷物
WO2018131422A1 (ja)	2017-01-13	2018-07-19	東洋インキＳｃホールディングス株式会社	液体現像剤、及び印刷物の製造方法
WO2019230539A1 (ja)	2018-05-31	2019-12-05	東洋インキＳｃホールディングス株式会社	着色組成物、および固体撮像素子用カラーフィルタの製造方法

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
IT1154630B (it) *	1982-12-06	1987-01-21	Montedison Spa	Pigmenti gialli compositi fotostabili e processo per la loro preparazione

1979
- 1979-10-26 JP JP13770779A patent/JPS5661461A/ja active Granted

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
EP1676889A1 (en)	2004-12-03	2006-07-05	Toyo Ink Mfg. Co., Ltd.	Colored composition
WO2008099879A1 (ja)	2007-02-16	2008-08-21	Toppan Printing Co., Ltd.	リターデイション基板、その製造方法及び液晶表示装置
US8665404B2 (en)	2007-12-21	2014-03-04	Nitto Denko Corporation	Liquid crystal cell substrate, liquid crystal cell, liquid crystal panel, and liquid crystal display
WO2009122621A1 (ja)	2008-03-31	2009-10-08	凸版印刷株式会社	位相差板、その製造方法及び液晶表示装置
WO2014061747A1 (ja)	2012-10-17	2014-04-24	東洋インキＳｃホールディングス株式会社	液体現像剤用高分子分散剤、液体現像剤、及び印刷物
WO2018131422A1 (ja)	2017-01-13	2018-07-19	東洋インキＳｃホールディングス株式会社	液体現像剤、及び印刷物の製造方法
WO2019230539A1 (ja)	2018-05-31	2019-12-05	東洋インキＳｃホールディングス株式会社	着色組成物、および固体撮像素子用カラーフィルタの製造方法

Also Published As

Publication number	Publication date
JPS5661461A (en)	1981-05-26

Publication	Publication Date	Title
US4310359A (en)	1982-01-12	Pigment compositions
JPS6088185A (ja)	1985-05-17	顔料分散剤
JPS6317101B2 (ko)	1988-04-12
JPH0134269B2 (ko)	1989-07-18
JPH10245501A (ja)	1998-09-14	顔料組成物およびその製造方法
KR20050006208A (ko)	2005-01-15	안료계 잉크 및 페인트의 레올로지를 향상시키기 위한조성물 및 방법
JPH049192B2 (ko)	1992-02-19
JPS63305173A (ja)	1988-12-13	顔料分散剤
JP2507810B2 (ja)	1996-06-19	顔料分散剤，顔料組成物，塗料および印刷インキ
JPS6317102B2 (ko)	1988-04-12
JPH0572943B2 (ko)	1993-10-13
JP2503468B2 (ja)	1996-06-05	ジスアゾ顔料組成物
JPH07110923B2 (ja)	1995-11-29	顔料組成物及び顔料分散体
JP3389808B2 (ja)	2003-03-24	顔料組成物およびその製造方法
JPH0118948B2 (ko)	1989-04-07
EP0595857A1 (en)	1994-05-11	Mixed coupled azo pigments
JPH0735484B2 (ja)	1995-04-19	顔料の分散方法および顔料組成物
JPH0217219B2 (ko)	1990-04-19
JPH0252659B2 (ko)	1990-11-14
JPH04246469A (ja)	1992-09-02	顔料組成物
JPH0673302A (ja)	1994-03-15	顔料分散剤
JPH0662876B2 (ja)	1994-08-17	モノアゾレーキ顔料の製造方法
JPH0134270B2 (ko)	1989-07-18
JPS59193125A (ja)	1984-11-01	顔料分散剤
JPH0134271B2 (ko)	1989-07-18

JPS6317102B2 - - Google Patents

Info

Links

Landscapes

Priority Applications (1)

Applications Claiming Priority (1)

Publications (2)

Family

ID=15204935

Family Applications (1)

Country Status (1)

Cited By (7)

Families Citing this family (1)

Cited By (7)

Also Published As

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