GB611235A - Process for the manufacture of new condensation products - Google Patents

Process for the manufacture of new condensation products

Info

Publication number
GB611235A
GB611235A GB583046A GB583046A GB611235A GB 611235 A GB611235 A GB 611235A GB 583046 A GB583046 A GB 583046A GB 583046 A GB583046 A GB 583046A GB 611235 A GB611235 A GB 611235A
Authority
GB
United Kingdom
Prior art keywords
dicyandiamide
condensed
treated
formaldehyde
copper
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
GB583046A
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.)
Sandoz AG
Original Assignee
Sandoz 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 Sandoz AG filed Critical Sandoz AG
Priority to GB583046A priority Critical patent/GB611235A/en
Publication of GB611235A publication Critical patent/GB611235A/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
    • D06P1/44General 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 insoluble pigments or auxiliary substances, e.g. binders
    • D06P1/52General 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 insoluble pigments or auxiliary substances, e.g. binders using compositions containing synthetic macromolecular substances
    • D06P1/56Condensation products or precondensation products prepared with aldehydes

Landscapes

  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

Resinous condensation products are prepared by condensing hydroxyalkyl - guanidines or biguanides or salts thereof with aldehydes or substances acting as such, preferably in the presence of salts of nitrogenous bases, e.g. ammonium chloride or ethylenediamine or ethanolamine hydrochlorides. The hydroxy-alkyl bodies may be prepared by condensing cyanamide, dicyandiamide, guanidine or biguanide with hydroxy-alkyl amines (e.g. ethanolamines, propanolamines, or those obtained by the action of ammonia or mono- or poly-valent amines, e.g. diethylenetriamine, on halogen-hydrins of glycol or glycerol or on epihalogen-hydrins, e.g. glycol- and glycerol-monochlorhydrins and glycerol-dichlorhydrin) or hydroxyalkylating agents (e.g. alkylene oxides or glycolor glycerol-halohydrins). In modifications, cyanamide, dicyandiamide, guanidine, biguanide are condensed with aldehydes in the presence of the above hydroxyamines or their salts or followed by treatment with the above hydroxy-alkylating agents. The condensation products may be treated in the presence of water with salts or compounds of polyvalent metals, e.g. copper, chromium, manganese, iron, cobalt, nickel, antimony, titanium, vanadium, tin, zinc or aluminium. The condensation products and their metal complexes improve the fastness to washing and perspiration of substantive dyeings on cellulosic fibres. In examples: (1), (3) glycolmonochlorhydrin or glycerol-dichlorhydrin is condensed with ammonia and the product with dicyandiamide and formaldehyde, and the condensate is treated with copper formate; (2) glycerolmonochlorhydrin is condensed with the same bodies and the product treated with copper chloride; (4) glyceroldichlorhydrin is condensed with diethylenetriamine and the product with dicyandiamide and formaldehyde, and the condensate is treated with copper acetate; (5) monoethanolamine hydrochloride is condensed with dicyandiamide and formaldedyde used simultaneously or successively; (6), (7) dicyandiamide is reacted with hydrogen chloride, and the product treated with ethylene oxide followed by formaldehyde or vice versa, and the condensate is treated with (6) copper acetate or (7) copper formate; (8) 1-phenylamino-2-hydroxy-3-aminopropane hydrochloride, dicyandiamide and formaldehyde are condensed; (9), (10) 1-amino-2-hydroxy-3-propylpiperidine hydrochloride, dicyandiamide and formaldehyde are condensed and the condensate may be treated with copper formate; (11), (12) 1 : 3-diamino-2-hydroxypropane hydrochloride, di-cyandiamide and formaldehyde are condensed, and the condensate may be treated with copper chloride. Samples have been furnished under Sect. 2 (5) as follows: the reaction product of a : g -glyceroldichlorhydrin and ammonia is reacted with (1), (2) dicyandiamide or (3), (4) guanidine carbonate, the product condensed with formaldehyde and the product treated with (1) vanadium dichloride, (2) potassium antimonyl tartrate, (3) copper chloride or (4) chromium trichloride. The Provisional Specification refers broadly to the condensation with aldehydes of "hydroxylated derivatives possessing amino or imino groups" or their salts, and to treatment with compounds of metals in general. The "hydroxylated derivatives" may be prepared from hydrocyanic acid, cyanuric acid and cyanuric acid chloride as well as from cyanamide &c., as described above.
GB583046A 1946-02-25 1946-02-25 Process for the manufacture of new condensation products Expired GB611235A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB583046A GB611235A (en) 1946-02-25 1946-02-25 Process for the manufacture of new condensation products

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB583046A GB611235A (en) 1946-02-25 1946-02-25 Process for the manufacture of new condensation products

Publications (1)

Publication Number Publication Date
GB611235A true GB611235A (en) 1948-10-27

Family

ID=9803413

Family Applications (1)

Application Number Title Priority Date Filing Date
GB583046A Expired GB611235A (en) 1946-02-25 1946-02-25 Process for the manufacture of new condensation products

Country Status (1)

Country Link
GB (1) GB611235A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3014073A (en) * 1956-04-23 1961-12-19 John A Gallaghan 1, 3-bis(nitroguanidino)-2-nitroxypropane, 1, 3-bis(guanidinium)-2-hydroxy propane and the preparation thereof
US3198595A (en) * 1965-08-03 Step-wise process for coloring anb fin- ishing cellulose materials wherein a cationic dye-fixing agent is employed with the resin finishing agent

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3198595A (en) * 1965-08-03 Step-wise process for coloring anb fin- ishing cellulose materials wherein a cationic dye-fixing agent is employed with the resin finishing agent
US3014073A (en) * 1956-04-23 1961-12-19 John A Gallaghan 1, 3-bis(nitroguanidino)-2-nitroxypropane, 1, 3-bis(guanidinium)-2-hydroxy propane and the preparation thereof

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