GB893748A - New dyestuff derivatives and their manufacture and use - Google Patents

New dyestuff derivatives and their manufacture and use

Info

Publication number
GB893748A
GB893748A GB677559A GB677559A GB893748A GB 893748 A GB893748 A GB 893748A GB 677559 A GB677559 A GB 677559A GB 677559 A GB677559 A GB 677559A GB 893748 A GB893748 A GB 893748A
Authority
GB
United Kingdom
Prior art keywords
dyestuff
acid
groups
water
urea
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
GB677559A
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 Schweiz AG
Original Assignee
Ciba 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 Ciba AG filed Critical Ciba AG
Publication of GB893748A publication Critical patent/GB893748A/en
Expired legal-status Critical Current

Links

Classifications

    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06PDYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
    • D06P1/00General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed
    • D06P1/0056Dyeing with polymeric dyes involving building the polymeric dyes on the fibres
    • D06P1/0064Dyeing with polymeric dyes involving building the polymeric dyes on the fibres by using reactive polyfunctional compounds, e.g. crosslinkers
    • 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
    • C09B69/00Dyes not provided for by a single group of this subclass
    • C09B69/10Polymeric dyes; Reaction products of dyes with monomers or with macromolecular compounds
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06PDYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
    • D06P1/00General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed
    • D06P1/38General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using reactive dyes

Landscapes

  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Structural Engineering (AREA)
  • Coloring (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)

Abstract

A water-soluble organic dyestuff containing at least one substituent capable of reacting with alkylol groups, is reacted with the components of an aminoplast precondensate which contains alkylol groups. The reactive groups in the dyestuff may for example be N-alkylol, or HN2 groups especially those bound to a 1,3,5-triazine ring, or to carbonyl group, aliphatic hydrocarbon radical, heterocyclic or aromatic ring), acrylic or chlorocrylic acid residues, vinyl sulphone groups or epoxy groups. Many other groups (are also mentioned in the specification as suitable. The dyestuffs may be of any class. Advantageously they also contain water-solubilizing groups e.g. carboxy or sulphonic. The products are useful for dyeing textiles from aqueous baths, which may contain in addition to the dyestuff derivative, an aminoplast, watersoluble or -dispersible monomers or polymers, e.g. polyvinyl alcohol, copolymers of esters or nitriles of unsaturated acids, and a small proportion of the free acid, or vinyl esters of saturated lower fatty acids, water-repellent materials, e.g. as described in Specification 781,265, and acid hardening catalysts, e.g. ammonium sulphate, diammonium phosphate, zinc nitrate, zinc fluorborate, ammonium silicofluoride, tartaric or formic acid. Printing preparation containing the dyestuff derivatives may also contain thickeners, e.g. starch, tragacanth, and hydrotropic substances, e.g. urea. The dyed or printed materials are dried and heated if desired with steam to cure the resins. In the Examples (1), (2), (6) a dyestuff of formula <FORM:0893748/IV (a)/1> is reacted in aqueous alkaline solution with urea and formaldehyde. In a second stage, methanol and hydrochloric acid are added and reaction continued. In Example (3), a dyestuff of formula <FORM:0893748/IV (a)/2> was used. In Example (7), melamine and formaldehyde are condensed in aqueous alkaline solution with a dyestuff of formula <FORM:0893748/IV (a)/3> and the product is etherified, in an acid second stage, with methanol. Example (8) is similar to Example (3), but the etherification step is omitted, and the dyestuff employed may, if desired, be of the formula <FORM:0893748/IV (a)/4> Example (9) is similar to Example (7) but uses one of the dyestuffs employed in Example (8). Example (10) is similar to Example (8) but uses the dyestuff employed in Example (7).ALSO:Dyestuff derivatives formed by reacting water soluble organic dyestuffs, containing substituents reacting with allylol groups, with the components of an aminoplast (see Group IV(a)) are used for dyeing or printing textile materials, whether made of animal, vegetable or synthetic fibres. The aqueous dyeing preparations may also contain aminoplasts which hav not been reacted with dyestuffs, water-soluble ordispersible monomers or polymers, e.g polyvinyl alcohol, copolymers of esters or nitriles of unsaturated acids and a small proportion of the free acid, or vinyl esters of lower fatty acids, water-repellent substances, e.g. as described in Specification 781,265, and hardening catalysts for the aminoplast. Printing preparations may also contain a thickener, e.g. starch, tragacanth, and a hydrotropic substance, e.g. urea. Dyein may be continuous and may be on a padding machine. The treated materials are dried and heated, if desired with steam to cure the resin. In certain circumstances the treatment may also render the material crease- or shrinkresistant or water-repellent. In Examples (1), (2) cotton fabric is padded with a solution of a dyestuff formed from urea, formaldehyde and a dye of formula <FORM:0893748/IV (c)/1> Ammonium sulphate is also present, and a methylol urea methyl ether or trimethylol melamine trimethyl ether may also be. The fabric is then heated. Example (3) is similar using a different dyestuff derivative. In Example (4) polyvinyl alcohol is included in the dye bath. In Example (5), the dyebath contains a dyestuff derivative according to the invention, acetic acid, trimethylol melamine trimethyl ether, ammonium sulphate, a condensate from stearic acid and hexamethylolmelamine hexamethyl ether and trithanolamine, a condensate from stearic acid and hexamethylol melamine hexamethyl ether and glycerol distearate, paraffin wax, chlorobenzene. In Example (6) the hardening catalyst employed is ammonium silicofluoride or tartaric acid. Example (7) uses a methylol melamine derivative of a dyestuff. The hardening catalyst may be ammonium silicofluoride, diammonium phosphate, zinc fluoborate, tartaric acid or zinc nitrate. Other examples are similar. In Example (11), a dyestuff derivative according to the invention is made up into a printing paste with ammonium sulphate, and a thickening agent prepared from oleyl alcohol and ethylene oxide and hexamethylene diisocyanate and sodium alginate, benzine and water.
GB677559A 1958-02-28 1959-02-26 New dyestuff derivatives and their manufacture and use Expired GB893748A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CH5648158A CH387193A (en) 1958-02-28 1958-02-28 Process for the production of new polycondensable dyes

Publications (1)

Publication Number Publication Date
GB893748A true GB893748A (en) 1962-04-11

Family

ID=4520529

Family Applications (1)

Application Number Title Priority Date Filing Date
GB677559A Expired GB893748A (en) 1958-02-28 1959-02-26 New dyestuff derivatives and their manufacture and use

Country Status (3)

Country Link
CH (1) CH387193A (en)
DE (1) DE1419776C3 (en)
GB (1) GB893748A (en)

Also Published As

Publication number Publication date
DE1419776A1 (en) 1968-10-17
DE1419776C3 (en) 1975-07-10
CH387193A (en) 1965-01-31
DE1419776B2 (en) 1974-11-28

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