GB971048A - Pigment dyes - Google Patents

Pigment dyes

Info

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
Application number
GB4315460A
Inventor
Guenther Riedel
Werner Deuschel
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.)
BASF SE
Original Assignee
BASF SE
Badische Anilin and Sodafabrik 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.)
Filing date
Publication date
Application filed by BASF SE, Badische Anilin and Sodafabrik AG filed Critical BASF SE
Publication of GB971048A publication Critical patent/GB971048A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D513/00Heterocyclic 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
    • C07D513/02Heterocyclic 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
    • C07D513/04Ortho-condensed systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D513/00Heterocyclic 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
    • C07D513/12Heterocyclic 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
    • C07D513/14Ortho-condensed systems
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00Use of organic ingredients
    • C08K5/16Nitrogen-containing compounds
    • C08K5/34Heterocyclic compounds having nitrogen in the ring
    • C08K5/3442Heterocyclic compounds having nitrogen in the ring having two nitrogen atoms in the ring
    • C08K5/3462Six-membered rings
    • C08K5/3465Six-membered rings condensed with carbocyclic rings
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09BORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B17/00Azine dyes
    • C09B17/005Dyes containing at least four ortho-condensed rings with at least two ring N-atoms in the system, e.g. fluoflavine, fluorubine, fluorindine
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09BORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B5/00Dyes with an anthracene nucleus condensed with one or more heterocyclic rings with or without carbocyclic rings
    • C09B5/24Dyes 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
    • C09B5/2409Dyes 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
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09BORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B57/00Other synthetic dyes of known constitution
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09BORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B67/00Influencing 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
    • C09B67/0071Process features in the making of dyestuff preparations; Dehydrating agents; Dispersing agents; Dustfree compositions
    • C09B67/0092Dyes in solid form

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.
GB4315460A 1957-12-19 1960-12-15 Pigment dyes Expired GB971048A (en)

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
GB4315560A Expired GB970471A (en) 1957-12-19 1960-12-15 Pigment dyes
GB4315460A Expired GB971048A (en) 1957-12-19 1960-12-15 Pigment dyes

Family Applications Before (2)

Application Number Title Priority Date Filing Date
GB1735464A Expired GB970472A (en) 1957-12-19 1960-12-15
GB4315560A Expired GB970471A (en) 1957-12-19 1960-12-15 Pigment dyes

Country Status (5)

Country Link
BE (1) BE598296A (en)
CH (2) CH409200A (en)
DE (1) DE1237243C2 (en)
FR (1) FR1278293A (en)
GB (3) GB970472A (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
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

Also Published As

Publication number Publication date
CH1364460A4 (en) 1963-03-29
DE1237243C2 (en) 1967-09-28
CH370387A (en) 1963-08-30
CH409200A (en) 1966-03-15
FR1278293A (en) 1961-12-08
GB970472A (en) 1964-09-23
DE1237243B (en) 1967-03-23
GB970471A (en) 1964-09-23
BE598296A (en) 1961-06-19

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