GB1055614A - Colour lakes - Google Patents

Colour lakes

Info

Publication number
GB1055614A
GB1055614A GB40853/64A GB4085364A GB1055614A GB 1055614 A GB1055614 A GB 1055614A GB 40853/64 A GB40853/64 A GB 40853/64A GB 4085364 A GB4085364 A GB 4085364A GB 1055614 A GB1055614 A GB 1055614A
Authority
GB
United Kingdom
Prior art keywords
acid
formaldehyde
mols
urea
dimethylolurea
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
GB40853/64A
Inventor
Otto Hertel
Walter Hensel
Hans Burkhardt
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 GB1055614A publication Critical patent/GB1055614A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D11/00Inks
    • C09D11/02Printing inks
    • C09D11/10Printing inks based on artificial resins
    • C09D11/102Printing inks based on artificial resins containing macromolecular compounds obtained by reactions other than those only involving unsaturated carbon-to-carbon bonds
    • C09D11/103Printing inks based on artificial resins containing macromolecular compounds obtained by reactions other than those only involving unsaturated carbon-to-carbon bonds of aldehydes, e.g. phenol-formaldehyde resins
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07GCOMPOUNDS OF UNKNOWN CONSTITUTION
    • C07G99/00Subject matter not provided for in other groups of this subclass
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G14/00Condensation polymers of aldehydes or ketones with two or more other monomers covered by at least two of the groups C08G8/00 - C08G12/00
    • C08G14/02Condensation polymers of aldehydes or ketones with two or more other monomers covered by at least two of the groups C08G8/00 - C08G12/00 of aldehydes
    • C08G14/04Condensation polymers of aldehydes or ketones with two or more other monomers covered by at least two of the groups C08G8/00 - C08G12/00 of aldehydes with phenols
    • C08G14/06Condensation polymers of aldehydes or ketones with two or more other monomers covered by at least two of the groups C08G8/00 - C08G12/00 of aldehydes with phenols and monomers containing hydrogen attached to nitrogen
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G14/00Condensation polymers of aldehydes or ketones with two or more other monomers covered by at least two of the groups C08G8/00 - C08G12/00
    • C08G14/02Condensation polymers of aldehydes or ketones with two or more other monomers covered by at least two of the groups C08G8/00 - C08G12/00 of aldehydes
    • C08G14/04Condensation polymers of aldehydes or ketones with two or more other monomers covered by at least two of the groups C08G8/00 - C08G12/00 of aldehydes with phenols
    • C08G14/06Condensation polymers of aldehydes or ketones with two or more other monomers covered by at least two of the groups C08G8/00 - C08G12/00 of aldehydes with phenols and monomers containing hydrogen attached to nitrogen
    • C08G14/08Ureas; Thioureas
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G14/00Condensation polymers of aldehydes or ketones with two or more other monomers covered by at least two of the groups C08G8/00 - C08G12/00
    • C08G14/02Condensation polymers of aldehydes or ketones with two or more other monomers covered by at least two of the groups C08G8/00 - C08G12/00 of aldehydes
    • C08G14/04Condensation polymers of aldehydes or ketones with two or more other monomers covered by at least two of the groups C08G8/00 - C08G12/00 of aldehydes with phenols
    • C08G14/12Chemically modified polycondensates
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G16/00Condensation polymers of aldehydes or ketones with monomers not provided for in the groups C08G4/00 - C08G14/00
    • C08G16/02Condensation polymers of aldehydes or ketones with monomers not provided for in the groups C08G4/00 - C08G14/00 of aldehydes
    • C08G16/0212Condensation polymers of aldehydes or ketones with monomers not provided for in the groups C08G4/00 - C08G14/00 of aldehydes with acyclic or carbocyclic organic compounds
    • C08G16/0218Condensation polymers of aldehydes or ketones with monomers not provided for in the groups C08G4/00 - C08G14/00 of aldehydes with acyclic or carbocyclic organic compounds containing atoms other than carbon and hydrogen
    • CCHEMISTRY; METALLURGY
    • C14SKINS; HIDES; PELTS; LEATHER
    • C14CCHEMICAL TREATMENT OF HIDES, SKINS OR LEATHER, e.g. TANNING, IMPREGNATING, FINISHING; APPARATUS THEREFOR; COMPOSITIONS FOR TANNING
    • C14C3/00Tanning; Compositions for tanning
    • C14C3/02Chemical tanning
    • C14C3/08Chemical tanning by organic agents
    • C14C3/18Chemical tanning by organic agents using polycondensation products or precursors thereof

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • General Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Materials Engineering (AREA)
  • Wood Science & Technology (AREA)
  • Color Printing (AREA)
  • Phenolic Resins Or Amino Resins (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Coloring (AREA)
  • Inks, Pencil-Leads, Or Crayons (AREA)

Abstract

A colour lake consists essentially of a basic dye and an alkali-soluble condensation product which is obtained by reacting in an acid aqueous medium (a) 2-5 mols. of an aromatic hydroxy compound, (b) 1-6 mols. of urea, alkylurea or alkylene urea or a methylol or methylol ether derivative thereof, (c) 1-6 mols. of an aromatic mononuclear carboxylic, sulphonic, aminocarboxylic, aminosulphonic or hydroxycarboxylic acid or an aliphatic dicarboxylic acid or an aryloxy fatty acid, and (d) 9-11 mols. of formaldehyde or a compound yielding formaldehyde, the formaldehyde preferably amounting to 38-50 mol. per cent of the total. Suitable compounds are (a) phenol, the cresols, 4-t-butylphenol, thymol, a - and b -naphthols. pyrocatechol (empyreumatic oils), partly methylated pyrocatechol, resorcinol, hydroquinone, 2- and 4-hydroxydiphenyl, 4,41-dihydroxy-diphenyl-methane, -propane and -sulphone, 4-hydroxydiphenylsulphone and phenylhydroxynaphthylsulphone, (b) urea, methylurea, N,N1-dimethylurea, ethyleneurea, propyleneurea, and acetylenediurea, and preferably methylol or dimethylolureas and alkyl ethers thereof, when (d) is correspondingly reduced, (c) benzoic acid, benzenesulphonic acid, p-toluenesulphonic acid, anthranilic acid, sulphanilic acid, 2-hydroxy-4-aminobenzoic acid, salicylic acid, gallic acid, malonic acid, glutaric acid and phenoxyacetic acid, (d) free formaldehyde, formalin, 1,3,5-trioxane, paraformaldehyde and hexamethylene tetramine. The condensation is preferably conducted between 30 DEG C. and the reflux point. The products may be washed with hot water and dried in vacuo, or on a roller or in a spray dryer. They are soluble, e.g. in methanol, ethanol, ethylene glycol, and acetone, and may be used as laking agents for basic dyes, e.g. auramine, rhodamine, Victoria Blue, methyl violet and crystal violet dyes and malachite green, to be used in carbon paper waxes, lithographic compositions and ballpoint pen inks. In examples, hydroxy diphenylsulphone, phenol or 4,41-dihydroxy-diphenylsulphone, plus thymol, resorcinol, hydroquinone, 2 - hydroxydiphenyl or p - t - butyl-phenol, and salicylic acid, and dimethylolurea or a urea-formaldehyde mixture are added to concentrated HCl and refluxed. In other examples, benzoic, anthranilic, sulphanilic or salicylic acid and dimethylolurea or its methyl ether or dimethylol ethyleneurea are added separately to the reaction product of 4,41-dihydroxydiphenylsulphone or p-t-butylphenol with formalin in hydrochloric acid solution. A flexographic printing ink containing 30 parts of a styrene/diethyl maleate copolymer, 90 of ethanol, 10 of ethylene glycol, 7 of rhodamine B and 14 of a hydroxydiphenylsulphone/thymol/ salicylic acid/dimethylolurea condensate is described.
GB40853/64A 1963-10-11 1964-10-07 Colour lakes Expired GB1055614A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DEB73834A DE1232975B (en) 1963-10-11 1963-10-11 Process for the production of alkali-soluble condensation products
DEB74751A DE1247328B (en) 1963-10-11 1963-12-20 Process for the production of alkali-soluble condensation products

Publications (1)

Publication Number Publication Date
GB1055614A true GB1055614A (en) 1967-01-18

Family

ID=25966814

Family Applications (1)

Application Number Title Priority Date Filing Date
GB40853/64A Expired GB1055614A (en) 1963-10-11 1964-10-07 Colour lakes

Country Status (5)

Country Link
AT (1) AT252260B (en)
CH (1) CH436333A (en)
DE (2) DE1232975B (en)
GB (1) GB1055614A (en)
NL (1) NL6411716A (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2843233C2 (en) * 1978-10-04 1985-07-18 Basf Ag, 6700 Ludwigshafen Tanning agent and its uses
DE3402265A1 (en) * 1984-01-24 1985-08-01 Basf Ag, 6700 Ludwigshafen AMPHOTERIC CONDENSATION PRODUCTS AND THEIR APPLICATION IN TEMPERATURE

Also Published As

Publication number Publication date
DE1247328B (en) 1967-08-17
CH436333A (en) 1967-05-31
AT252260B (en) 1967-02-10
DE1232975B (en) 1967-01-26
NL6411716A (en) 1965-04-12

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