GB466345A - Improvements in the manufacture and production of nitrogenous products - Google Patents

Improvements in the manufacture and production of nitrogenous products

Info

Publication number
GB466345A
GB466345A GB825037A GB825037A GB466345A GB 466345 A GB466345 A GB 466345A GB 825037 A GB825037 A GB 825037A GB 825037 A GB825037 A GB 825037A GB 466345 A GB466345 A GB 466345A
Authority
GB
United Kingdom
Prior art keywords
products
condensation
acid
sulphonic
methylethyleneimine
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
GB825037A
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.)
IG Farbenindustrie AG
Original Assignee
IG Farbenindustrie 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 IG Farbenindustrie AG filed Critical IG Farbenindustrie AG
Priority to GB825037A priority Critical patent/GB466345A/en
Publication of GB466345A publication Critical patent/GB466345A/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
    • C08G73/00Macromolecular compounds obtained by reactions forming a linkage containing nitrogen with or without oxygen or carbon in the main chain of the macromolecule, not provided for in groups C08G12/00 - C08G71/00
    • C08G73/02Polyamines
    • C08G73/0206Polyalkylene(poly)amines
    • C08G73/0213Preparatory process

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Coloring (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

Assistants useful in the textile, leather, lacquer, rubber, pharmaceutical and cosmetic industries are obtained when mono or polymeric 1 : 2-alkyleneimines are condensed with halogenated aromatic compounds or aromatic sulphonic acid halides. The treatment of monomeric ethyleneimine or N-methylethyleneimine with benzenesulphonic or toluene acid chloride in the presence of sodium hydroxide is, however disclaimed. The reaction may be combined with a condensation with aldehydes or ketones, (cf. Specification 466,346), or with other substances capable of condensation, e.g. urea, dimethylolurea, thiourea, phenols, cetylamine, octodecylamine, styrene, synthetic rubber or synthetic resins. The condensation may be effected in the presence of solvents or diluents such as water, alcohol, ether, cyclohexanone, toluene, carbontetrachloride or chlorbenzene. Acyl, sulphonic, sulphuric ester, carboxylic or phosphoric acid groups may be introduced into the products or into the reacting components. The products may be added in dyeing, printing, washing, dressing, stripping, fulling, levelling, tanning, dispersing and wetting processes. They may also be used in softening and flotation agents, and to increase the affinity of viscose and copper artificial silk for acid dyestuffs. They may be added to spinning solutions and the products obtained with the co-employment of aldehydes or ketones may be used for dressing textiles, leather, paper or straw and for rendering artificial silk crease- and slide-proof. Dispersing agents such as sulphuric esters of fatty alcohols and aliphatic sulphonic acids may be used with the products, which can also be employed in the form of salts with mineral or organic, e.g. fatty acids. The condensation products may be produced directly on the fibre, such as wool, cotton, cellulose acetate or viscose or copper artificial silk. In examples: (1) butyl ethyleneimine is condensed with 2 : 4-dinitro-1-chlorbenzene; the product as well as the diamino compound obtained by reduction may be used in the production of copper or viscose artificial silk; (2) polymeric ethylene imine is reacted with toluenesulphonic acid chloride or p-nitrobenzyl chloride; the product may be treated with chlorethanesulphonic acid or sulphonating agents. Further specified imines are methylethyleneimine, a : b -butyleneimine, o -chlor-a : b - butyleneimine and dodecyleneimine. Specification 466,344 also is referred to.ALSO:Products which may be added to preparations used as dispersing agents are obtained when mono or polymeric 1 : 2-alkyleneimines are condensed with halogenated aromatic compounds or aromatic sulphonic acid halides. The treatment of monomeric ethyleneimine or N-methylethyleneimine with benzenesulphonic or toluene acid chloride in the presence of sodium hydroxide is, however, disclaimed. The reaction may be combined with a condensation with aldehydes or ketones (cf. Specification 466,346), or with other substances capable of condensation, e.g. urea, dimethylolurea, thiourea, phenols, cetylamine, octodecylamine, styrene, synthetic rubber or synthetic resins. Acyl, sulphonic, sulphuric ester, carboxylic or phosphoric acid groups may be introduced into the products or into the reacting components. Dispersing agents such as sulphuric esters of fatty alcohols and aliphatic sulphonic acids may be used with the products, which can also be employed in the form of salts with mineral or organic, e.g. fatty, acids. In examples: (1) butylethyleneimine is condensed with 2 : 4-dinitro-1-chlorbenzene; (2) polymeric ethylene imine is reacted with toluenesulphonic acid chloride or p-nitrobenzyl chloride; the product may be treated with chlorethanesulphonic acid or sulphonating agents. Further specified imines are methylethyleneimine, a : b -butyleneimine, o -chlor-a : b -butyleneimine and dodecyleneimine. Specification 466,344 also is referred to.
GB825037A 1935-08-22 1935-08-22 Improvements in the manufacture and production of nitrogenous products Expired GB466345A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB825037A GB466345A (en) 1935-08-22 1935-08-22 Improvements in the manufacture and production of nitrogenous products

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB825037A GB466345A (en) 1935-08-22 1935-08-22 Improvements in the manufacture and production of nitrogenous products

Publications (1)

Publication Number Publication Date
GB466345A true GB466345A (en) 1937-05-24

Family

ID=9848889

Family Applications (1)

Application Number Title Priority Date Filing Date
GB825037A Expired GB466345A (en) 1935-08-22 1935-08-22 Improvements in the manufacture and production of nitrogenous products

Country Status (1)

Country Link
GB (1) GB466345A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3203910A (en) * 1962-04-13 1965-08-31 Dow Chemical Co Polymerization of alkylenimines
US3345253A (en) * 1963-08-30 1967-10-03 Hoechst Ag Process of forming cellulosic webs containing urea-alkyleneimine condensation products

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3203910A (en) * 1962-04-13 1965-08-31 Dow Chemical Co Polymerization of alkylenimines
US3345253A (en) * 1963-08-30 1967-10-03 Hoechst Ag Process of forming cellulosic webs containing urea-alkyleneimine condensation products

Similar Documents

Publication Publication Date Title
US2328901A (en) Nitrogenous condensation product
US2182306A (en) Polymerization of ethylene imines
US2213477A (en) Glycol and polyglycol ethers of isocyclic hydroxyl compounds
GB466344A (en) Improvements in the manufacture and production of nitrogenous products
GB655258A (en) Process for improving materials in the form of fibre or film and manufacture of coumarin derivatives for use therein
US2249757A (en) Alkyl hydroxy aromatic sulphonate
US2185163A (en) Polyoxyalkylene ammonium compounds and process of preparing them
US1990588A (en) Artificial fibroin thread
GB465200A (en) Improvements in the manufacture and production of valuable condensation products containing nitrogen, phosphorus or sulphur
GB466345A (en) Improvements in the manufacture and production of nitrogenous products
GB466270A (en) Improvements in the manufacture and production of nitrogenous products
US2637622A (en) Formaldehyde-dicyandiamide resins and the treatment of leather therewith
US2256877A (en) Wetting, penetrating, foaming, and dispersing agent
GB343901A (en) Improvements in the manufacture and production of wetting, cleansing and dispersing agents
FR2462510A1 (en) PROCESS FOR DYEING CELLULOSE FIBERS
US2051389A (en) Fulling fabrics
US2993915A (en) Tetrahydrofuryl and tetrahydrofurfuryl glycidyl ethers
US1933945A (en) Production of urethane substances
US2275006A (en) Manufacture of phthalic acid-monophenyl-amides
US2008649A (en) Aliphatic poly-amides and process
US2195186A (en) Process for the production of sulphonated fatty acids
GB466346A (en) Improvements in the manufacture and production of nitrogenous products
US2079973A (en) Water-soluble sulphonation products of phosphatides, and process for preparing same
US2114256A (en) Sulphuric acid derivatives of higher molecular organic amines
GB378383A (en) Improvements in the manufacture and production of wetting, cleansing, dispersing andthe like agents