DE2063714B2 - - Google Patents
Info
- Publication number
- DE2063714B2 DE2063714B2 DE2063714A DE2063714A DE2063714B2 DE 2063714 B2 DE2063714 B2 DE 2063714B2 DE 2063714 A DE2063714 A DE 2063714A DE 2063714 A DE2063714 A DE 2063714A DE 2063714 B2 DE2063714 B2 DE 2063714B2
- Authority
- DE
- Germany
- Prior art keywords
- perylene
- amino
- pigment
- tetracarboxylic acid
- acid diimide
- 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 claims description 15
- 238000000227 grinding Methods 0.000 claims description 11
- PONZBUKBFVIXOD-UHFFFAOYSA-N 9,10-dicarbamoylperylene-3,4-dicarboxylic acid Chemical compound C=12C3=CC=C(C(O)=O)C2=C(C(O)=O)C=CC=1C1=CC=C(C(O)=N)C2=C1C3=CC=C2C(=N)O PONZBUKBFVIXOD-UHFFFAOYSA-N 0.000 claims description 10
- 150000003839 salts Chemical class 0.000 claims description 7
- -1 aliphatic amines Chemical class 0.000 claims description 6
- 238000000034 method Methods 0.000 claims description 6
- 238000004040 coloring Methods 0.000 claims description 5
- 238000010348 incorporation Methods 0.000 claims 1
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 6
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- 239000000203 mixture Substances 0.000 description 6
- 239000003973 paint Substances 0.000 description 6
- 239000004793 Polystyrene Substances 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- 238000009835 boiling Methods 0.000 description 3
- JRBPAEWTRLWTQC-UHFFFAOYSA-N dodecylamine Chemical compound CCCCCCCCCCCCN JRBPAEWTRLWTQC-UHFFFAOYSA-N 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 239000003960 organic solvent Substances 0.000 description 3
- 239000011780 sodium chloride Substances 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- FJLUATLTXUNBOT-UHFFFAOYSA-N 1-Hexadecylamine Chemical compound CCCCCCCCCCCCCCCCN FJLUATLTXUNBOT-UHFFFAOYSA-N 0.000 description 2
- SAIKULLUBZKPDA-UHFFFAOYSA-N Bis(2-ethylhexyl) amine Chemical compound CCCCC(CC)CNCC(CC)CCCC SAIKULLUBZKPDA-UHFFFAOYSA-N 0.000 description 2
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- REYJJPSVUYRZGE-UHFFFAOYSA-N Octadecylamine Chemical compound CCCCCCCCCCCCCCCCCCN REYJJPSVUYRZGE-UHFFFAOYSA-N 0.000 description 2
- 239000004952 Polyamide Substances 0.000 description 2
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- PLZVEHJLHYMBBY-UHFFFAOYSA-N Tetradecylamine Chemical compound CCCCCCCCCCCCCCN PLZVEHJLHYMBBY-UHFFFAOYSA-N 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- 239000001110 calcium chloride Substances 0.000 description 2
- 229910001628 calcium chloride Inorganic materials 0.000 description 2
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 2
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
- RAABOESOVLLHRU-UHFFFAOYSA-N diazene Chemical compound N=N RAABOESOVLLHRU-UHFFFAOYSA-N 0.000 description 2
- 229910000071 diazene Inorganic materials 0.000 description 2
- 238000004043 dyeing Methods 0.000 description 2
- XLHBQRJOHIHZGQ-UHFFFAOYSA-N heptadecan-9-amine Chemical compound CCCCCCCCC(N)CCCCCCCC XLHBQRJOHIHZGQ-UHFFFAOYSA-N 0.000 description 2
- LQNUZADURLCDLV-UHFFFAOYSA-N nitrobenzene Chemical compound [O-][N+](=O)C1=CC=CC=C1 LQNUZADURLCDLV-UHFFFAOYSA-N 0.000 description 2
- 239000004033 plastic Substances 0.000 description 2
- 229920003023 plastic Polymers 0.000 description 2
- 229920002647 polyamide Polymers 0.000 description 2
- 229920000915 polyvinyl chloride Polymers 0.000 description 2
- 239000004800 polyvinyl chloride Substances 0.000 description 2
- 229910052938 sodium sulfate Inorganic materials 0.000 description 2
- 235000011152 sodium sulphate Nutrition 0.000 description 2
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 2
- 239000004753 textile Substances 0.000 description 2
- 239000002966 varnish Substances 0.000 description 2
- 238000010626 work up procedure Methods 0.000 description 2
- WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 description 1
- XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 description 1
- PRIUALOJYOZZOJ-UHFFFAOYSA-L 2-ethylhexyl 2-[dibutyl-[2-(2-ethylhexoxy)-2-oxoethyl]sulfanylstannyl]sulfanylacetate Chemical compound CCCCC(CC)COC(=O)CS[Sn](CCCC)(CCCC)SCC(=O)OCC(CC)CCCC PRIUALOJYOZZOJ-UHFFFAOYSA-L 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 235000013162 Cocos nucifera Nutrition 0.000 description 1
- 244000060011 Cocos nucifera Species 0.000 description 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- MHZGKXUYDGKKIU-UHFFFAOYSA-N Decylamine Chemical compound CCCCCCCCCCN MHZGKXUYDGKKIU-UHFFFAOYSA-N 0.000 description 1
- 208000000655 Distemper Diseases 0.000 description 1
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 1
- 239000004640 Melamine resin Substances 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- AMQJEAYHLZJPGS-UHFFFAOYSA-N N-Pentanol Chemical compound CCCCCO AMQJEAYHLZJPGS-UHFFFAOYSA-N 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 229920000297 Rayon Polymers 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 229920000180 alkyd Polymers 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 239000003945 anionic surfactant Substances 0.000 description 1
- 239000011324 bead Substances 0.000 description 1
- XJHABGPPCLHLLV-UHFFFAOYSA-N benzo[de]isoquinoline-1,3-dione Chemical compound C1=CC(C(=O)NC2=O)=C3C2=CC=CC3=C1 XJHABGPPCLHLLV-UHFFFAOYSA-N 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000003093 cationic surfactant Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 235000019864 coconut oil Nutrition 0.000 description 1
- 239000003240 coconut oil Substances 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- HPXRVTGHNJAIIH-UHFFFAOYSA-N cyclohexanol Chemical compound OC1CCCCC1 HPXRVTGHNJAIIH-UHFFFAOYSA-N 0.000 description 1
- 150000004985 diamines Chemical class 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 239000011888 foil Substances 0.000 description 1
- 239000000976 ink Substances 0.000 description 1
- 229910017053 inorganic salt Inorganic materials 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- 239000004922 lacquer Substances 0.000 description 1
- 229920002521 macromolecule Polymers 0.000 description 1
- 235000012054 meals Nutrition 0.000 description 1
- 238000013508 migration Methods 0.000 description 1
- 230000005012 migration Effects 0.000 description 1
- 238000003801 milling Methods 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- 239000011368 organic material Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- XNGIFLGASWRNHJ-UHFFFAOYSA-L phthalate(2-) Chemical compound [O-]C(=O)C1=CC=CC=C1C([O-])=O XNGIFLGASWRNHJ-UHFFFAOYSA-L 0.000 description 1
- 230000019612 pigmentation Effects 0.000 description 1
- 230000000485 pigmenting effect Effects 0.000 description 1
- 229920002239 polyacrylonitrile Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 239000010453 quartz Substances 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 239000008096 xylene 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
- C09B67/0001—Post-treatment of organic pigments or dyes
- C09B67/002—Influencing the physical properties by treatment with an amine
-
- 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
- C09B5/00—Dyes with an anthracene nucleus condensed with one or more heterocyclic rings with or without carbocyclic rings
- C09B5/62—Cyclic imides or amidines of peri-dicarboxylic acids of the anthracene, benzanthrene, or perylene series
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Paints Or Removers (AREA)
- Coloring (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Priority Applications (8)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE2063714A DE2063714C3 (de) | 1970-12-24 | 1970-12-24 | Verfahren zur Überführung von Perylen-S^-SMO-tetracarbonsäurediimid in eine als Pigmentfarbstoff verwendbare Form |
| CH1863971A CH533163A (de) | 1970-12-24 | 1971-12-20 | Verfahren zur Überführung von Perylen-3,4,9,10-tetracarbonsäurediimid in einer als Pigmentfarbstoff verwendbaren Form |
| IT54922/71A IT945588B (it) | 1970-12-24 | 1971-12-22 | Procedimento per trasformare diim mide di acido perilen 3, 4, 9, 10 tetracarbossilico in una forma di pigmento |
| GB5993671A GB1321349A (en) | 1970-12-24 | 1971-12-23 | Process for the conversion of perylene-3,4,9,10-tetracarboxylic acid diimide into a form suitable as pigment dyestuff |
| BE777230A BE777230A (fr) | 1970-12-24 | 1971-12-23 | Procede pour convertir le diimide de l'acide perylene 3,4,9,10-tetracarboxylique en une forme utilisable comme colorant pigmentaire |
| NL7117770A NL7117770A (en, 2012) | 1970-12-24 | 1971-12-23 | |
| US00211681A US3752686A (en) | 1970-12-24 | 1971-12-23 | Process for the conversion of perylene-3,4,9,10 - tetracarboxylic acid diimide into a form suitable as pigment dyestuff |
| FR7146639A FR2119752A5 (en, 2012) | 1970-12-24 | 1971-12-24 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE2063714A DE2063714C3 (de) | 1970-12-24 | 1970-12-24 | Verfahren zur Überführung von Perylen-S^-SMO-tetracarbonsäurediimid in eine als Pigmentfarbstoff verwendbare Form |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| DE2063714A1 DE2063714A1 (de) | 1972-06-29 |
| DE2063714B2 true DE2063714B2 (en, 2012) | 1979-01-25 |
| DE2063714C3 DE2063714C3 (de) | 1979-10-11 |
Family
ID=5792114
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE2063714A Expired DE2063714C3 (de) | 1970-12-24 | 1970-12-24 | Verfahren zur Überführung von Perylen-S^-SMO-tetracarbonsäurediimid in eine als Pigmentfarbstoff verwendbare Form |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US3752686A (en, 2012) |
| BE (1) | BE777230A (en, 2012) |
| CH (1) | CH533163A (en, 2012) |
| DE (1) | DE2063714C3 (en, 2012) |
| FR (1) | FR2119752A5 (en, 2012) |
| GB (1) | GB1321349A (en, 2012) |
| IT (1) | IT945588B (en, 2012) |
| NL (1) | NL7117770A (en, 2012) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2316536C3 (de) * | 1973-04-03 | 1981-08-20 | Basf Ag, 6700 Ludwigshafen | Verfahren zur Herstellung von farbstarken und leicht verteilbaren Perylen- 3,4,9,10-tetracarbonsäurediimiden |
| DE2962612D1 (en) * | 1978-05-18 | 1982-06-09 | Ciba Geigy Ag | Process for batch-colouring hard pvc and polyolefines |
| DE2837731A1 (de) | 1978-08-30 | 1980-03-13 | Basf Ag | Verfahren zur herstellung von pigmentformen des perylen-3,4,9,10-tetracarbonsaeurediimids mit hoher lasur und brillanz |
| US5019473A (en) * | 1990-02-23 | 1991-05-28 | Eastman Kodak Company | Electrophotographic recording elements containing photoconductive perylene pigments |
| US5141837A (en) * | 1990-02-23 | 1992-08-25 | Eastman Kodak Company | Method for preparing coating compositions containing photoconductive perylene pigments |
-
1970
- 1970-12-24 DE DE2063714A patent/DE2063714C3/de not_active Expired
-
1971
- 1971-12-20 CH CH1863971A patent/CH533163A/de not_active IP Right Cessation
- 1971-12-22 IT IT54922/71A patent/IT945588B/it active
- 1971-12-23 NL NL7117770A patent/NL7117770A/xx unknown
- 1971-12-23 GB GB5993671A patent/GB1321349A/en not_active Expired
- 1971-12-23 BE BE777230A patent/BE777230A/xx unknown
- 1971-12-23 US US00211681A patent/US3752686A/en not_active Expired - Lifetime
- 1971-12-24 FR FR7146639A patent/FR2119752A5/fr not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| FR2119752A5 (en, 2012) | 1972-08-04 |
| IT945588B (it) | 1973-05-10 |
| DE2063714C3 (de) | 1979-10-11 |
| BE777230A (fr) | 1972-06-23 |
| NL7117770A (en, 2012) | 1972-06-27 |
| GB1321349A (en) | 1973-06-27 |
| CH533163A (de) | 1973-01-31 |
| US3752686A (en) | 1973-08-14 |
| DE2063714A1 (de) | 1972-06-29 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| EP0254681A2 (de) | Neue Stoffzusammensetzungen auf der Basis von Indanthronblau-Pigmenten | |
| DE1914271A1 (de) | Verfahren zur Herstellung farbstarker transparenter Pigmente der Isoindolinreihe | |
| DE2302509A1 (de) | Disazopigment, verfahren zu seiner herstellung und seine verwendung | |
| DE2256485C3 (de) | Kupferphthalocyaninpigmente sowie ihre Verwendung | |
| DE2302481B2 (de) | Disazopigment, Verfahren zu seiner Herstellung und seiner Verwendung | |
| DE2063714C3 (de) | Verfahren zur Überführung von Perylen-S^-SMO-tetracarbonsäurediimid in eine als Pigmentfarbstoff verwendbare Form | |
| EP0008063B1 (de) | Azomethinderivate von Anthrachinonen, Verfahren zu deren Herstellung; deren Verwendung zum Pigmentieren organischer makromolekularer Stoffe und die so erhaltenen Materialien | |
| DE1807729A1 (de) | Farbstoff der Perylentetracorbonsaeurediimidreihe | |
| DE1257096B (de) | Verwendung zweier neuer Modifikationen des Perylen-3, 4, 9, 10-tetracarbonsaeure-bis-(4-phenylazo)-phenylimids als Pigmente | |
| DE2743095A1 (de) | Anthrachinonverbindungen, verfahren zu deren herstellung sowie deren verwendung | |
| DE2247009C3 (de) | Iminoisoindolinonfarbstoffe und Verwendung zum Pigmentieren von hochmolekularem organischem Material | |
| DE2043482C3 (de) | Monoazopigment, Verfahren zu seiner Herstellung und Verwendung | |
| DE2518892B2 (de) | Iminoisoindolinonpigmente, Verfahren zu deren Herstellung und ihre Verwendung | |
| DE1569773B1 (de) | Pigment der Bis-(tetrachlor-isoindolin-l-on-3-ylidenimino)-aryl-reihe und Verfahren zu dessen Herstellung | |
| DE2520011A1 (de) | Neue iminoisoindolinonpigmente und verfahren zu deren herstellung | |
| DE2012505B2 (de) | Kupfer- und nickelphthalocyanin- mischkondensat-pigmente | |
| DE929992C (de) | Verfahren zur Herstellung von gefaerbtem Polyvinylbenzal | |
| DE2012507C3 (de) | Verfahren zur Herstellung von Phthalocyaninpigmenten und ihre Verwendung als Pigmente für Lacke, Druck' farben, Leim- und Binderfarben, sowie zum Masse- und Spinnfärben von makromolekularen Stoffen und künstlichen Fasern | |
| DE2804062A1 (de) | Neue stabile modifikation eines isoindolinon-pigments, verfahren zu deren herstellung und deren verwendung | |
| DE2400561A1 (de) | Iminoisoindolinonfarbstoffe und verfahren zu deren herstellung | |
| DE1812004C3 (de) | Modifikationen des Tetrabrom-8,8'-dihydroxy-naphthazins, ihre Herstellung und ihre Verwendung als Pigmentfarbstoffe | |
| DE1569773C (de) | Pigment der Bis (tetrachlor isoindo Im 1 on 3 yhdenimino) aryl reihe und Verfahren zu dessen Herstellung | |
| DE2513578C3 (de) | 2,6-Dioxy-3-cyan-4-methylpyridin-Disazofarbstoff, Verfahren zu seiner Herstellung und seine Verwendung für Druckfarben und Lacke | |
| DE1494081A1 (de) | Verfahren zum Pigmentieren von makromolekularen organischen Stoffen | |
| DE2847661A1 (de) | Neue modifikation eines disazopigmentes |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| C3 | Grant after two publication steps (3rd publication) | ||
| 8339 | Ceased/non-payment of the annual fee |