GB971048A - Pigment dyes - Google Patents
Pigment dyesInfo
- Publication number
- GB971048A GB971048A GB4315460A GB4315460A GB971048A GB 971048 A GB971048 A GB 971048A GB 4315460 A GB4315460 A GB 4315460A GB 4315460 A GB4315460 A GB 4315460A GB 971048 A GB971048 A GB 971048A
- Authority
- GB
- United Kingdom
- Prior art keywords
- ring
- give
- formula
- yellow
- pigments
- 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.)
- Expired
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D513/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
- C07D513/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
- C07D513/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D513/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
- C07D513/12—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains three hetero rings
- C07D513/14—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/16—Nitrogen-containing compounds
- C08K5/34—Heterocyclic compounds having nitrogen in the ring
- C08K5/3442—Heterocyclic compounds having nitrogen in the ring having two nitrogen atoms in the ring
- C08K5/3462—Six-membered rings
- C08K5/3465—Six-membered rings condensed with carbocyclic rings
-
- 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
- C09B17/00—Azine dyes
- C09B17/005—Dyes containing at least four ortho-condensed rings with at least two ring N-atoms in the system, e.g. fluoflavine, fluorubine, fluorindine
-
- 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
- C09B5/24—Dyes with an anthracene nucleus condensed with one or more heterocyclic rings with or without carbocyclic rings the heterocyclic rings being only condensed with an anthraquinone nucleus in 1-2 or 2-3 position
- C09B5/2409—Dyes with an anthracene nucleus condensed with one or more heterocyclic rings with or without carbocyclic rings the heterocyclic rings being only condensed with an anthraquinone nucleus in 1-2 or 2-3 position not provided for in one of the sub groups C09B5/26 - C09B5/62
-
- 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
- C09B57/00—Other synthetic dyes of known constitution
-
- 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
- C09B67/0071—Process features in the making of dyestuff preparations; Dehydrating agents; Dispersing agents; Dustfree compositions
- C09B67/0092—Dyes in solid form
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Coloring (AREA)
- Paints Or Removers (AREA)
- Inks, Pencil-Leads, Or Crayons (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Abstract
Plaster of Paris and cement are coloured red with a pigment of the formula <FORM:0971048/C1/1>ALSO:In examples, a pigment of the formula <FORM:0971048/C3/1> (2) wherein X is NH and rings A and D are each linearly fused with benzene rings, is ground with nitrocellulose, dibutyl phthalate and an ethyl alcohol/ethyl glycol mixture to give a yellow printing colour; (3) wherein X is 0, is mixed with a lacquer containing nitrocellulose, dibutylphthalate, benzyl butyl phthalate, the product obtained by treating cyclohexanone with sodium hydroxide, butyl acetate, methyl acetate, and toluene to give a greenish-yellow lacquer, (pigments wherein X is NH, ring D forms part of a phenazine residue and ring A may or may not be linearly fused to a benzene ring may also be used); (4) wherein X is NH, ring D forms part of a phenazine residue and ring A is linearly fused to a benzene ring, is ground with xylene and a mixture of linseed oil and the esterification product from phthalic acid, glycerin and pentaerythritol to give a red-orange lacquer; (5) wherein X is NH and ring D is linearly fused to a benzene ring, is ground with an unsaturated polyester resin drying without the aid of paraffin and then mixed with monostyrene, a cyclohexanone peroxide paste in dibutyl phthalate, cobalt naphthenate in white spirit and silicone oil in xylene to give a yellow paint for wood; (6) wherein X is 0 and ring D forms part of an anthraquinone residue, is mixed with polyvinyl chloride, di-isooctyl phthalate and titanium dioxide to give a red polyvinyl chloride; and (7) wherein X is NH, is mixed and homogenised with polystyrene granulate or polyethylene to give a yellow plastic.ALSO:Quinoxaline derivatives of the formula <FORM:0971048/C4-C5/1> wherein X is NH, O or S and which may carry substituents and/or other rings fused linearly or angularly are made by heating a 2 : 3-dichlorquinoxaline at a temperature above about 125 DEG C. with an appropriate o-diamino-, o-amino-hydroxy- or o-amino-mercapto-aromatic or heterocyclic compound at a mol. ratio of about 1 : 1 using a carboxylic acid-N : N-dialkylamide as a solvent. The invention also comprises pigments of the above formula wherein X is NH, O or S and which may be substituted and/or have linearly fused rings, having a mean particle size in the range of from 0.02 to 1 micron. The pigments may be made by the process above and then if necessray be subjected to salt-milling or acid-pasting. When additional fused rings are present these may be such that ring A in the formula above also forms part of a naphthalene nucleus and/or ring D also forms part of naphthalene, anthracene, anthraquinone or phenazine nuclei. The pigments colour a variety of materials. In examples (1) a yellow printing ink is made by grinding aluminium hydroxide and a linseed oil varnish with one of a number of pigments of the above general formula, and a yellow wall-paper colour is made by mixing a paste of a pigment of the above general formula where a benzene ring is linearly fused to ring D with heavy spar, aluminium sulphate, sodium carbonate and water, adding barium chloride and mixing the precipitate obtained with glue solution.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE1957B0055975 DE1237243C2 (en) | 1957-12-19 | 1957-12-19 | Use of quinoxal derivatives as pigment dyes |
Publications (1)
Publication Number | Publication Date |
---|---|
GB971048A true GB971048A (en) | 1964-09-30 |
Family
ID=6971166
Family Applications (3)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB1735464A Expired GB970472A (en) | 1957-12-19 | 1960-12-15 | |
GB4315460A Expired GB971048A (en) | 1957-12-19 | 1960-12-15 | Pigment dyes |
GB4315560A Expired GB970471A (en) | 1957-12-19 | 1960-12-15 | Pigment dyes |
Family Applications Before (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB1735464A Expired GB970472A (en) | 1957-12-19 | 1960-12-15 |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB4315560A Expired GB970471A (en) | 1957-12-19 | 1960-12-15 | Pigment dyes |
Country Status (5)
Country | Link |
---|---|
BE (1) | BE598296A (en) |
CH (2) | CH370387A (en) |
DE (1) | DE1237243C2 (en) |
FR (1) | FR1278293A (en) |
GB (3) | GB970472A (en) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB0520539D0 (en) | 2005-10-08 | 2005-11-16 | Avecia Inkjet Ltd | Process compound, ink and use |
DE102007050673A1 (en) * | 2007-10-19 | 2009-04-23 | Friedrich-Schiller-Universität Jena | New hexaaza-acene compounds comprising three pyrazine-annelated and additional benzo-annelated rings, useful as fluorescence dye in biochemical medical diagnostics, and as transistor in organic semiconductor technology |
-
1957
- 1957-12-19 DE DE1957B0055975 patent/DE1237243C2/en not_active Expired
-
1960
- 1960-12-06 CH CH1364460A patent/CH370387A/en unknown
- 1960-12-06 CH CH1364360A patent/CH409200A/en unknown
- 1960-12-15 GB GB1735464A patent/GB970472A/en not_active Expired
- 1960-12-15 GB GB4315460A patent/GB971048A/en not_active Expired
- 1960-12-15 GB GB4315560A patent/GB970471A/en not_active Expired
- 1960-12-19 BE BE598296A patent/BE598296A/en unknown
- 1960-12-19 FR FR847311A patent/FR1278293A/en not_active Expired
Also Published As
Publication number | Publication date |
---|---|
CH409200A (en) | 1966-03-15 |
DE1237243B (en) | 1967-03-23 |
CH370387A (en) | 1963-08-30 |
GB970471A (en) | 1964-09-23 |
BE598296A (en) | 1961-06-19 |
FR1278293A (en) | 1961-12-08 |
DE1237243C2 (en) | 1967-09-28 |
GB970472A (en) | 1964-09-23 |
CH1364460A4 (en) | 1963-03-29 |
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