CH623348A5 - Phthalocyanine pigment compositions - Google Patents

Phthalocyanine pigment compositions Download PDF

Info

Publication number: CH623348A5
Authority: CH; Switzerland
Prior art keywords: parts; pigment; phthalocyanine; composition according; groups
Prior art date: 1975-09-09

Application number

CH1132876A

Other languages

German (de)

English (en)

Inventor

Ian Robert Wheeler

George Heddle Dr Robertson

Original Assignee

Ciba Geigy Ag

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.)

1975-09-09

Filing date

1976-09-07

Publication date

1981-05-29

1975-09-09 Priority claimed from GB37106/75A external-priority patent/GB1501184A/en

1976-05-07 Priority claimed from GB1873676A external-priority patent/GB1541599A/en

1976-09-07 Application filed by Ciba Geigy Ag filed Critical Ciba Geigy Ag

1981-05-29 Publication of CH623348A5 publication Critical patent/CH623348A5/de

Links

239000000049 pigment Substances 0.000 title claims description 37
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 title claims description 22
239000000203 mixture Substances 0.000 title claims description 21
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 claims description 12
239000001007 phthalocyanine dye Substances 0.000 claims description 11
125000000217 alkyl group Chemical group 0.000 claims description 10
125000003118 aryl group Chemical group 0.000 claims description 10
125000003710 aryl alkyl group Chemical group 0.000 claims description 7
125000004432 carbon atom Chemical group C* 0.000 claims description 6
125000002015 acyclic group Chemical group 0.000 claims description 5
125000004122 cyclic group Chemical group 0.000 claims description 5
-1 urethane compound Chemical class 0.000 claims description 5
JVVXZOOGOGPDRZ-SLFFLAALSA-N [(1R,4aS,10aR)-1,4a-dimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthren-1-yl]methanamine Chemical compound NC[C@]1(C)CCC[C@]2(C)C3=CC=C(C(C)C)C=C3CC[C@H]21 JVVXZOOGOGPDRZ-SLFFLAALSA-N 0.000 claims description 4
125000000542 sulfonic acid group Chemical group 0.000 claims description 4
JOYRKODLDBILNP-UHFFFAOYSA-N urethane group Chemical group NC(=O)OCC JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 claims description 4
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 3
125000003277 amino group Chemical group 0.000 claims description 2
125000000753 cycloalkyl group Chemical group 0.000 claims description 2
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 2
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 2
238000000034 method Methods 0.000 description 12
239000003973 paint Substances 0.000 description 11
239000006185 dispersion Substances 0.000 description 10
150000001875 compounds Chemical class 0.000 description 9
239000002904 solvent Substances 0.000 description 8
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 6
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
239000001055 blue pigment Substances 0.000 description 5
239000002002 slurry Substances 0.000 description 5
PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 4
XCJYREBRNVKWGJ-UHFFFAOYSA-N copper(II) phthalocyanine Chemical compound [Cu+2].C12=CC=CC=C2C(N=C2[N-]C(C3=CC=CC=C32)=N2)=NC1=NC([C]1C=CC=CC1=1)=NC=1N=C1[C]3C=CC=CC3=C2[N-]1 XCJYREBRNVKWGJ-UHFFFAOYSA-N 0.000 description 4
150000003839 salts Chemical class 0.000 description 4
QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 3
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 3
HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 3
229920000180 alkyd Polymers 0.000 description 3
238000000227 grinding Methods 0.000 description 3
238000011065 in-situ storage Methods 0.000 description 3
229910052751 metal Inorganic materials 0.000 description 3
239000002184 metal Substances 0.000 description 3
230000007935 neutral effect Effects 0.000 description 3
JVTCNOASZYIKTG-UHFFFAOYSA-N stk329495 Chemical compound [Cu].[N-]1C(N=C2C3=CC=CC=C3C(N=C3C4=CC=CC=C4C(=N4)[N-]3)=N2)=C(C=CC=C2)C2=C1N=C1C2=CC=CC=C2C4=N1 JVTCNOASZYIKTG-UHFFFAOYSA-N 0.000 description 3
150000003673 urethanes Chemical class 0.000 description 3
ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 2
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 2
RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 2
230000015572 biosynthetic process Effects 0.000 description 2
229910052801 chlorine Inorganic materials 0.000 description 2
239000000460 chlorine Substances 0.000 description 2
229910017052 cobalt Inorganic materials 0.000 description 2
239000010941 cobalt Substances 0.000 description 2
GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 2
230000000052 comparative effect Effects 0.000 description 2
229910052802 copper Inorganic materials 0.000 description 2
239000010949 copper Substances 0.000 description 2
NLFBCYMMUAKCPC-KQQUZDAGSA-N ethyl (e)-3-[3-amino-2-cyano-1-[(e)-3-ethoxy-3-oxoprop-1-enyl]sulfanyl-3-oxoprop-1-enyl]sulfanylprop-2-enoate Chemical compound CCOC(=O)\C=C\SC(=C(C#N)C(N)=O)S\C=C\C(=O)OCC NLFBCYMMUAKCPC-KQQUZDAGSA-N 0.000 description 2
239000007788 liquid Substances 0.000 description 2
238000004519 manufacturing process Methods 0.000 description 2
229910052759 nickel Inorganic materials 0.000 description 2
239000002245 particle Substances 0.000 description 2
239000000843 powder Substances 0.000 description 2
YBBRCQOCSYXUOC-UHFFFAOYSA-N sulfuryl dichloride Chemical compound ClS(Cl)(=O)=O YBBRCQOCSYXUOC-UHFFFAOYSA-N 0.000 description 2
LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 description 2
229910052723 transition metal Inorganic materials 0.000 description 2
150000003624 transition metals Chemical class 0.000 description 2
239000002699 waste material Substances 0.000 description 2
229910052725 zinc Inorganic materials 0.000 description 2
239000011701 zinc Substances 0.000 description 2
SZUVGFMDDVSKSI-WIFOCOSTSA-N (1s,2s,3s,5r)-1-(carboxymethyl)-3,5-bis[(4-phenoxyphenyl)methyl-propylcarbamoyl]cyclopentane-1,2-dicarboxylic acid Chemical group O=C([C@@H]1[C@@H]([C@](CC(O)=O)([C@H](C(=O)N(CCC)CC=2C=CC(OC=3C=CC=CC=3)=CC=2)C1)C(O)=O)C(O)=O)N(CCC)CC(C=C1)=CC=C1OC1=CC=CC=C1 SZUVGFMDDVSKSI-WIFOCOSTSA-N 0.000 description 1
ALSTYHKOOCGGFT-KTKRTIGZSA-N (9Z)-octadecen-1-ol Chemical compound CCCCCCCC\C=C/CCCCCCCCO ALSTYHKOOCGGFT-KTKRTIGZSA-N 0.000 description 1
APLNAFMUEHKRLM-UHFFFAOYSA-N 2-[5-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]-1,3,4-oxadiazol-2-yl]-1-(3,4,6,7-tetrahydroimidazo[4,5-c]pyridin-5-yl)ethanone Chemical group C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)C1=NN=C(O1)CC(=O)N1CC2=C(CC1)N=CN2 APLNAFMUEHKRLM-UHFFFAOYSA-N 0.000 description 1
125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 description 1
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
239000000020 Nitrocellulose Substances 0.000 description 1
IGFHQQFPSIBGKE-UHFFFAOYSA-N Nonylphenol Natural products CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 description 1
125000001931 aliphatic group Chemical group 0.000 description 1
150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
125000003282 alkyl amino group Chemical group 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
150000001408 amides Chemical group 0.000 description 1
150000001412 amines Chemical class 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
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 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
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 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
238000004821 distillation Methods 0.000 description 1
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
229910052736 halogen Inorganic materials 0.000 description 1
150000002367 halogens Chemical class 0.000 description 1
125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
229910052739 hydrogen Inorganic materials 0.000 description 1
239000001257 hydrogen Substances 0.000 description 1
239000000976 ink Substances 0.000 description 1
229920001220 nitrocellulos Polymers 0.000 description 1
SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 1
125000002347 octyl 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])[H] 0.000 description 1
229940055577 oleyl alcohol Drugs 0.000 description 1
XMLQWXUVTXCDDL-UHFFFAOYSA-N oleyl alcohol Natural products CCCCCCC=CCCCCCCCCCCO XMLQWXUVTXCDDL-UHFFFAOYSA-N 0.000 description 1
125000000913 palmityl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
150000003254 radicals Chemical class 0.000 description 1
238000010992 reflux Methods 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
125000001424 substituent group Chemical group 0.000 description 1
125000000565 sulfonamide group Chemical group 0.000 description 1
DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 description 1
239000002966 varnish 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
- 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
- C09B67/0035—Mixtures of phthalocyanines
- 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
- C09B69/00—Dyes not provided for by a single group of this subclass
- C09B69/02—Dyestuff salts, e.g. salts of acid dyes with basic dyes
- C09B69/04—Dyestuff salts, e.g. salts of acid dyes with basic dyes of anionic dyes with nitrogen containing compounds

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Chemical Kinetics & Catalysis (AREA)
Inks, Pencil-Leads, Or Crayons (AREA)
Compositions Of Macromolecular Compounds (AREA)
Paints Or Removers (AREA)
Coloring (AREA)

CH1132876A 1975-09-09 1976-09-07 Phthalocyanine pigment compositions CH623348A5 (en)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
GB37106/75A GB1501184A (en)	1975-09-09	1975-09-09	Phthalocyanine pigment composition
GB1873676A GB1541599A (en)	1976-05-07	1976-05-07	Pigment composition

Publications (1)

Publication Number	Publication Date
CH623348A5 true CH623348A5 (en)	1981-05-29

Family

ID=26253579

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CH1132876A CH623348A5 (en)	1975-09-09	1976-09-07	Phthalocyanine pigment compositions

Country Status (6)

Country	Link
JP (1)	JPS6059264B2 (da)
CA (1)	CA1080907A (da)
CH (1)	CH623348A5 (da)
DE (1)	DE2640063A1 (da)
DK (1)	DK403976A (da)
FR (1)	FR2355885A1 (da)

Families Citing this family (11)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
GB1575562A (en) *	1977-03-19	1980-09-24	Ciba Geigy Ag	Pigment composition
US4522654A (en) *	1983-12-23	1985-06-11	Inmont Corporation	Continuous method of producing phthalocyanine pigment dispersions in organic solvent
JPH01284867A (ja) *	1988-05-11	1989-11-16	Sharp Corp	電子写真プリンター装置
CH685162A5 (de) *	1991-05-07	1995-04-13	Ciba Geigy Ag	Pigmentzusammensetzungen.
JP2836320B2 (ja) *	1991-10-04	1998-12-14	東洋インキ製造株式会社	塗料組成物
JP3132231B2 (ja) *	1993-04-23	2001-02-05	東洋インキ製造株式会社	顔料組成物および印刷インキもしくは塗料組成物
AU3386195A (en) *	1995-08-18	1997-03-12	Bayer Aktiengesellschaft	Microbicidal formulations
JPH08240945A (ja) *	1996-01-23	1996-09-17	Sanyo Electric Co Ltd	Ｌｅｄプリンタ
CN1281490A (zh) *	1997-12-09	2001-01-24	日本化药株式会社	新的盐类及含有该盐类的光敏性着色树脂组合物
DE102008026584A1 (de) *	2008-06-03	2009-12-10	Clariant International Limited	Verbessertes Cyanfarbmittel
WO2019124050A1 (ja) *	2017-12-22	2019-06-27	Dic株式会社	銅フタロシアニン顔料組成物及びこれを有するインキ組成物

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4057436A (en) *	1974-09-17	1977-11-08	Imperial Chemical Industries Limited	Dispersion of solids in organic solvents
DE3111052C2 (de) *	1981-03-20	1985-03-07	Ciba-Geigy GmbH, 7867 Wehr	Distanzfolie für den Formen- und Modellbau sowie ihre Verwendung
JPS5916580A (ja) *	1982-07-17	1984-01-27	コンピユ−タ−サ−ビス株式会社	選別装置の通口遮蔽機構

1976
- 1976-09-06 DE DE19762640063 patent/DE2640063A1/de not_active Ceased
- 1976-09-07 CA CA260,622A patent/CA1080907A/en not_active Expired
- 1976-09-07 CH CH1132876A patent/CH623348A5/de not_active IP Right Cessation
- 1976-09-08 DK DK403976A patent/DK403976A/da not_active Application Discontinuation
- 1976-09-09 FR FR7627101A patent/FR2355885A1/fr active Granted
- 1976-09-09 JP JP51108376A patent/JPS6059264B2/ja not_active Expired

Also Published As

Publication number	Publication date
DE2640063A1 (de)	1977-03-17
JPS5233922A (en)	1977-03-15
FR2355885B1 (da)	1980-10-03
FR2355885A1 (fr)	1978-01-20
JPS6059264B2 (ja)	1985-12-24
CA1080907A (en)	1980-07-08
DK403976A (da)	1977-03-10

Legal Events

Date	Code	Title	Description
1984-05-30	PL	Patent ceased
2024-10-31	PL	Patent ceased

Publication	Publication Date	Title
DE3305571C2 (da)	1991-02-28
EP0511165A2 (de)	1992-10-28	Neue Diketopyrrolopyrrolverbindungen
DE2554252A1 (de)	1977-06-16	Verfahren zur ueberfuehrung von rohkupferphthalocyaninen in eine pigmentform
DE2103030C3 (de)	1979-11-29	Verfahren zur Pigmentbehandlung
DE2308594A1 (de)	1973-08-30	Bisazomethinpigment und verfahren zu seiner herstellung
DE2531823A1 (de)	1976-02-05	Gegenueber kristallisation stabile phthalocyaninpigmente
EP0273866A2 (de)	1988-07-06	Neue Stoffzusammensetzungen auf der Basis von C.I. Pigment Rot 177
DE2312147A1 (de)	1973-09-27	Phthalocyanin-pigmente
DE2640063A1 (de)	1977-03-17	Pigmentzusammensetzungen
DE3542437A1 (de)	1986-06-19	Pulverpigment mit verbesserten rheologischen eigenschaften, verfahren zu ihrer herstellung und ihre verwendung mit einem gehalt von mindestens 5 % unsubstituiertem chinacridon
CH630946A5 (de)	1982-07-15	Phthalocyaninpigmentpraeparate und verfahren zu deren herstellung.
DE2727531C2 (da)	1990-02-15
DE1444195A1 (de)	1968-12-05	Nichtflockende und loesungsmittelechte Phthalocyaninpigmentgemische
DE1444274A1 (de)	1969-03-27	Verfahren zur Herstellung von Pigmentmassen
CH644391A5 (de)	1984-07-31	Verfahren zur herstellung eines isoindolinon-pigments.
DE2811539C2 (da)	1988-02-04
DE2720464C2 (da)	1988-07-07
DE1619618C3 (de)	1973-10-04	Chinacridon-Pigmentmasse
EP0445072B1 (de)	1996-03-27	Herstellung metallisierter Azopigmente
DE2406332B2 (de)	1980-06-26	Phthalocyanine, Verfahren zu ihrer Herstellung und ihre Verwendung
CH629523A5 (de)	1982-04-30	Verfahren zur herstellung von kupferphthalocyaninderivaten.
DE2739775C2 (da)	1987-12-03
DE1285445B (de)	1968-12-19	Pigmentmasse
DE1592876A1 (de)	1970-12-23	Verfahren zur UEberfuehrung von Farbstoffen aus der Reihe der Arylpararosanilinsulfonsaeuren in coloristisch wertvolle Pigmente
DE1128065B (de)	1962-04-19	Verfahren zur Herstellung flockulationsbestaendiger Kupferphthalocyaninpigmente