GB486577A - Manufacture of condensation products from aminotriazines - Google Patents

Manufacture of condensation products from aminotriazines

Info

Publication number
GB486577A
GB486577A GB1184438A GB1184438A GB486577A GB 486577 A GB486577 A GB 486577A GB 1184438 A GB1184438 A GB 1184438A GB 1184438 A GB1184438 A GB 1184438A GB 486577 A GB486577 A GB 486577A
Authority
GB
United Kingdom
Prior art keywords
triazine
alcohol
glycerol
amino
acid
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
GB1184438A
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.)
Individual
Original Assignee
Individual
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 Individual filed Critical Individual
Priority to GB1184438A priority Critical patent/GB486577A/en
Publication of GB486577A publication Critical patent/GB486577A/en
Expired legal-status Critical Current

Links

Classifications

    • 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
    • C08G12/00Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen
    • C08G12/02Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen of aldehydes
    • C08G12/40Chemically modified polycondensates
    • C08G12/42Chemically modified polycondensates by etherifying
    • C08G12/424Chemically modified polycondensates by etherifying of polycondensates based on heterocyclic compounds
    • C08G12/425Chemically modified polycondensates by etherifying of polycondensates based on heterocyclic compounds based on triazines

Landscapes

  • Chemical & Material Sciences (AREA)
  • General Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Phenolic Resins Or Amino Resins (AREA)

Abstract

Condensation products are prepared by condensing an aminotriazine, a compound containing at least five carbon atoms and at least one alcoholic hydroxyl group, and an aldehyde or a substance yielding an aldehyde, all or part of the alcoholic compound being added after the reaction between the other compounds. Reactants specified include: aminotriazines-2 : 4 : 6 - triamino-1 : 3 : 5-triazine (melamine), 2-amino-1 : 3 : 5-triazine, 2 - amino - 4 - oxy - 6 - chloro-1 : 3 : 5-triazine, 2 - amino - 4 - oxy - 6 - phenyl - 1 : 3 : 5-triazine, 2 : 4-diamine-1 : 3 : 5-triazine, 2 : 4-diamine-6-p-oxyphenyl-1 : 3 : 5-triazine, 2-methylamino - 4 - amino - 6 - chloro - 1 : 3 : 5-triazine, 2 : 4-diamino-6-phenylamino-1 : 3 : 5-triazine, 2-amino-4 : 6-diphenylamino-1 : 3 : 5-triazine, 2 : 4 : 6 - trimethylamino - 1 : 3 : 5-triazine, 2 : 4 : 6 - triphenylamino - 1 : 3 : 5-triazine, 3-amino-1 : 2 : 4-phentriazoxine, melam, melem and melone; alcohols-aliphatic, aromatic, hydroaromatic or heterocyclic alcohols which may also contain other substituents (such as aldehyde, keto, carboxyl or amino groups or halogen atoms) or substances which under reaction conditions are converted into alcohols (such as acetals, esters, and enolizable keto compounds) such as ethylbutanol, ethylhexanol, lauryl alcohol, cetyl alcohol, stearyl alcohol, oleyl alcohol, mannitol, sorbitol, benzyl alcohol, terpineol, borneol, abietinol, wool fat alcohols, furfuryl alcohol, carbohydrates, glucose, cane sugar, trihexosane, dextrine, starches, gum arabic, gum tragacanth, ricinoleic acid, saccharic acid (or their esters), halogen alkyl alcohols, aminoalcohols, triethanolamine, glycerol monoethyl ether, glycerol diethyl ether, cyclohexanone-glycerol, glycerol mono- or di-esters of fatty acids, and alkyd resins (glycerol-phthalic acid, -sebacic acid or -adipic acid esters) containing free hydroxyl groups; aldehydes-formaldehyde, paraformaldehyde, trioxymethylene, acetaldehyde, crotonaldehyde, acrolein, benzaldehyde or furfural. Further substances capable of reacting with an amino group or an alcohol group (such as acid chlorides or acid anhydrides) or with an aldehyde group (such as amines, aniline, amides, urea, thiourea, sulphamides or phenols) may be present during the reaction or caused to react with the condensation product. Reactants containing other substituents (such as carboxyl, carbonyl, hydroxy, or amino groups or halogen atoms) may be further reacted by virtue of the substituents with such substances as acid chlorides or anhydrides, alcoholates, salts of carboxylic acids, amines or amides. The condensation products may be mixed with, condensed with, or made in the presence of, artificial or natural resins, dyestuffs, fillers, softeners, dehydrating agents or waterproofing agents. The products, which may be thermohardening or thermosetting (the latter being convertible into the former by reaction with aldehyde) may be used in the manufacture of moulding powders, moulded articles, binding agents, for glueing wood, paper, textile fabrics, for the production of artificial cork, artificial wood, for brush cements, for fixing colouring materials, for the production of insectides, for impregnating textile webs and forming laminated bodies therefrom, as lacquers and as addition to air-drying oils, for the manufacture of cast articles, and in the textile industry as finishes, non-creasing agents, for diminishing swelling capacity, as thickening, stiffening or softening agents, as agents for making fillers or finishes water-resistant and in the preparation of dyed or printed materials. In examples melamine is condensed with aqueous formaldehyde and the product treated with (1) benzyl alcohol; (2) methanol; (3) a mixture of ethyl alcohol and ethyl-2-hexanol; or (5) glycerol or glycol; (4) melamine is condensed with alcoholic formaldehyde and the product condensed with cetyl, lauryl, stearyl or oleyl alcohol, terpineol, wool fat alcohol, castor oil, diethyl tartrate, diethylin, glycerol-a -monochlorhydrin, or cyclohexanone glycerol; (6) melamine is condensed with aqueous formaldehyde and the dehydrated mass is mixed with glycerol and wood flour, hot kneaded, comminuted and moulded; (7) melamine is condensed with alcoholic formaldehyde and heated with (a) a mixture of ricinoleic acid monoglyceride, (b) benzene, alcohol and a resin prepared by condensing equimolecular proportions of glycerol and phthalic carhydride; (8) a condensate of melamine and alcoholic formaldehyde is heated with a solution in alcohol and benzene of a condensate of adipic acid and glycerol; (9) a condensation product of 3-amino-1 : 2 : 4-phentriazoxine and aqueous formaldehyde is heated with a mixture of glycol and ethyl-2-butanol.
GB1184438A 1936-10-28 1936-10-28 Manufacture of condensation products from aminotriazines Expired GB486577A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB1184438A GB486577A (en) 1936-10-28 1936-10-28 Manufacture of condensation products from aminotriazines

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB1184438A GB486577A (en) 1936-10-28 1936-10-28 Manufacture of condensation products from aminotriazines

Publications (1)

Publication Number Publication Date
GB486577A true GB486577A (en) 1938-05-30

Family

ID=9993719

Family Applications (1)

Application Number Title Priority Date Filing Date
GB1184438A Expired GB486577A (en) 1936-10-28 1936-10-28 Manufacture of condensation products from aminotriazines

Country Status (1)

Country Link
GB (1) GB486577A (en)

Cited By (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2416884A (en) * 1942-09-09 1947-03-04 Du Pont Methylated methylolmelamine as a fixing agent for dyed cotton textiles
US2426770A (en) * 1942-02-07 1947-09-02 American Cyanamid Co Textile finishing composition comprising a methoxymethyl melamine and an aliphatic alcohol having at least eight carbon atoms
US2447440A (en) * 1941-08-30 1948-08-17 American Cyanamid Co Amino substituted aryl guanamines
US2454078A (en) * 1941-04-09 1948-11-16 Du Pont Methylol melamine ethers and their manufacture
US2459397A (en) * 1941-08-30 1949-01-18 American Cyanamid Co Amino aliphatic guanamines
US2473463A (en) * 1947-05-22 1949-06-14 American Cyanamid Co Alkylated melamine-formaldehyde liquid compositions
US2474194A (en) * 1941-08-30 1949-06-21 American Cyanamid Co N-heterocyclic substituted guanamines
US2489352A (en) * 1946-04-10 1949-11-29 Merck & Co Inc Halogen compounds of 3 aminobenzotriazine 1, 2, 4 oxide-1
US2489351A (en) * 1946-04-10 1949-11-29 Merck & Co Inc Preparation of benzotriazine compounds
US2489356A (en) * 1947-01-10 1949-11-29 Merck & Co Inc Benzotriazines and process for preparing the same
US2489353A (en) * 1947-01-10 1949-11-29 Merck & Co Inc Benzotriazines
US2489354A (en) * 1947-01-10 1949-11-29 Merck & Co Inc Benzotriazines
US2661262A (en) * 1950-01-30 1953-12-01 Monsanto Chemicals Composition containing colloidal methyl ether of methylol melamine and other thermoplastic resins and process of applying to cellulose textiles

Cited By (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2454078A (en) * 1941-04-09 1948-11-16 Du Pont Methylol melamine ethers and their manufacture
US2474194A (en) * 1941-08-30 1949-06-21 American Cyanamid Co N-heterocyclic substituted guanamines
US2447440A (en) * 1941-08-30 1948-08-17 American Cyanamid Co Amino substituted aryl guanamines
US2459397A (en) * 1941-08-30 1949-01-18 American Cyanamid Co Amino aliphatic guanamines
US2426770A (en) * 1942-02-07 1947-09-02 American Cyanamid Co Textile finishing composition comprising a methoxymethyl melamine and an aliphatic alcohol having at least eight carbon atoms
US2416884A (en) * 1942-09-09 1947-03-04 Du Pont Methylated methylolmelamine as a fixing agent for dyed cotton textiles
US2489352A (en) * 1946-04-10 1949-11-29 Merck & Co Inc Halogen compounds of 3 aminobenzotriazine 1, 2, 4 oxide-1
US2489351A (en) * 1946-04-10 1949-11-29 Merck & Co Inc Preparation of benzotriazine compounds
US2489356A (en) * 1947-01-10 1949-11-29 Merck & Co Inc Benzotriazines and process for preparing the same
US2489353A (en) * 1947-01-10 1949-11-29 Merck & Co Inc Benzotriazines
US2489354A (en) * 1947-01-10 1949-11-29 Merck & Co Inc Benzotriazines
US2473463A (en) * 1947-05-22 1949-06-14 American Cyanamid Co Alkylated melamine-formaldehyde liquid compositions
US2661262A (en) * 1950-01-30 1953-12-01 Monsanto Chemicals Composition containing colloidal methyl ether of methylol melamine and other thermoplastic resins and process of applying to cellulose textiles

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