GB496611A - Basic derivatives of fatty acids and a process for their manufacture - Google Patents
Basic derivatives of fatty acids and a process for their manufactureInfo
- Publication number
- GB496611A GB496611A GB28923/37A GB2892337A GB496611A GB 496611 A GB496611 A GB 496611A GB 28923/37 A GB28923/37 A GB 28923/37A GB 2892337 A GB2892337 A GB 2892337A GB 496611 A GB496611 A GB 496611A
- Authority
- GB
- United Kingdom
- Prior art keywords
- glycerindichlorhydrin
- fat
- condensing
- salts
- condensed
- 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
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C215/00—Compounds containing amino and hydroxy groups bound to the same carbon skeleton
- C07C215/02—Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton
- C07C215/04—Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being saturated
- C07C215/06—Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being saturated and acyclic
- C07C215/14—Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being saturated and acyclic the nitrogen atom of the amino group being further bound to hydrocarbon groups substituted by amino groups
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01F—MIXING, e.g. DISSOLVING, EMULSIFYING OR DISPERSING
- B01F23/00—Mixing according to the phases to be mixed, e.g. dispersing or emulsifying
- B01F23/40—Mixing liquids with liquids; Emulsifying
- B01F23/41—Emulsifying
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S516/00—Colloid systems and wetting agents; subcombinations thereof; processes of
- Y10S516/01—Wetting, emulsifying, dispersing, or stabilizing agents
- Y10S516/07—Organic amine, amide, or n-base containing
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Coloring (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Abstract
Basic compounds are prepared by heating hydroxylated aliphatic polyamines obtained by condensing hydroxyalkylamines with : a -g glycerindichlorhydrin or epichlorhydrin, with a fatty acid containing at least eight carbon atoms or an ester thereof at a temperature of 150-250 DEG C., and converting the resulting products into soluble salts. The latter are stated to have wetting, foaming, cleansing and softening properties and may be used for increasing the fastness of substantive dyeings since they form insoluble addition products (lakes) with substantive dyestuffs. In examples: (1) monoethanol-amine is condensed with a -g -glycerindichlorhydrin and the product heated with coconut fat, olive oil, castor oil, hardened fat, beef tallow and a naphthenic acid mixture: the basic products are converted into salts with acetic or lactic acid; (2) diethanolamine is condensed with a : g : glycerindichlorhydrin and the product heated with coconut fat, hardened fat, spermacetti, and stearic acid and then converted into salts: (3) hardened fat is heated with a hydroxylated polyamine obtained by condensing monoethanolamine with a : g -glycerindichlorhydrin at 130 DEG C. and again condensing with a : g -glycerindichlorhydrin at 125 DEG C. after adding caustic soda and driving off water. The use of wool fat is mentioned. The Specification as open to inspection under Sect. 91 comprises also the use of triethanolamine and propanolamines in the preparation of the hydroxylated aliphatic polyamines and states that the use of higher temperatures produces quaternary-polyamines such as [ClN(C2H4OH)3CH]2CHOH. This subject-matter does not appear in the Specification as accepted.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH496611X | 1936-10-23 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB496611A true GB496611A (en) | 1938-12-02 |
Family
ID=4516763
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB28923/37A Expired GB496611A (en) | 1936-10-23 | 1937-10-22 | Basic derivatives of fatty acids and a process for their manufacture |
Country Status (4)
Country | Link |
---|---|
US (1) | US2149527A (en) |
CH (3) | CH191564A (en) |
FR (1) | FR828015A (en) |
GB (1) | GB496611A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2464094A (en) * | 1943-09-13 | 1949-03-08 | Lankro Chem Ltd | Process for the amidation of esters |
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 |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2792281A (en) * | 1953-09-21 | 1957-05-14 | American Viscose Corp | Viscose composition and method of spinning |
US2901430A (en) * | 1953-11-06 | 1959-08-25 | Gen Aniline & Film Corp | Corrosion inhibition |
US2994660A (en) * | 1957-05-27 | 1961-08-01 | Magnet Cove Barium Corp | Water-in-oil emulsion drilling fluid |
US3959156A (en) * | 1973-12-06 | 1976-05-25 | Sandoz, Inc. | Fabric softener |
-
1936
- 1936-10-23 CH CH191564D patent/CH191564A/en unknown
- 1936-10-23 CH CH195846D patent/CH195846A/en unknown
- 1936-10-23 CH CH195845D patent/CH195845A/en unknown
-
1937
- 1937-10-18 FR FR828015D patent/FR828015A/en not_active Expired
- 1937-10-19 US US169918A patent/US2149527A/en not_active Expired - Lifetime
- 1937-10-22 GB GB28923/37A patent/GB496611A/en not_active Expired
Cited By (2)
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 | ||
US2464094A (en) * | 1943-09-13 | 1949-03-08 | Lankro Chem Ltd | Process for the amidation of esters |
Also Published As
Publication number | Publication date |
---|---|
CH191564A (en) | 1937-06-30 |
FR828015A (en) | 1938-05-09 |
US2149527A (en) | 1939-03-07 |
CH195846A (en) | 1938-02-15 |
CH195845A (en) | 1938-02-15 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US1985424A (en) | Alkylene-oxide derivatives of polyhydroxyalkyl-alkylamides | |
JPH04506804A (en) | Production method of quaternary ammonium compound | |
US1923178A (en) | Hydroxy alkyl ethers of tertiary amines and process of preparing same | |
GB380431A (en) | Improvements in the manufacture and production of assistants in the textile and related industries and dispersing agents | |
GB496611A (en) | Basic derivatives of fatty acids and a process for their manufacture | |
GB420518A (en) | Textile assistants | |
GB418247A (en) | Improvement in emulsifying detergent and wetting agents | |
US2191978A (en) | Quaternary nitrogen compounds and process of preparing them | |
US1923179A (en) | Treatment of textiles and agents therefor | |
DE731981C (en) | Process for the production of condensation products | |
GB417654A (en) | Improvements in fulling fabrics | |
US2365265A (en) | Insoluble azo dyes | |
GB383634A (en) | The production of improved dyeings | |
GB451300A (en) | Improvements in the manufacture and production of aqueous dispersions of anhydrides of fatty acids of high molecular weight | |
GB414712A (en) | Improvements in the manufacture and production of substances suitable as wetting, washing, dispersing and like agents | |
GB434358A (en) | A process for the production of sulphuric acids of aliphatic amino-ethers of high molecular weight | |
DE800408C (en) | Process for the production of condensation products | |
GB485377A (en) | Improvements in the manufacture and production of aminoketones | |
GB448242A (en) | Manufacture of condensation products | |
GB494056A (en) | Process for the obtention of a thorough saponification during the production of a soap from highly split distilled fatty acids with concentrated soda lye in the open boiler | |
GB454183A (en) | A process of producing nucleus-substituted aliphatic-aromatic sulphonic acids | |
GB491163A (en) | A process for the manufacture of orthotolylbiguanide from orthotoluidine and dicyanodiamide | |
GB494625A (en) | New basic condensation products | |
GB361732A (en) | ||
GB359001A (en) | Improvements in the manufacture and production of valuable organic nitrogen compounds |