GB413457A - Manufacture of emulsifying, cleansing, wetting or softening agents - Google Patents
Manufacture of emulsifying, cleansing, wetting or softening agentsInfo
- Publication number
- GB413457A GB413457A GB11568/33A GB1156833A GB413457A GB 413457 A GB413457 A GB 413457A GB 11568/33 A GB11568/33 A GB 11568/33A GB 1156833 A GB1156833 A GB 1156833A GB 413457 A GB413457 A GB 413457A
- Authority
- GB
- United Kingdom
- Prior art keywords
- aliphatic
- condensed
- groups
- products
- ammonia
- 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
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
- D06M13/322—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing nitrogen
- D06M13/325—Amines
- D06M13/342—Amino-carboxylic acids; Betaines; Aminosulfonic acids; Sulfo-betaines
Landscapes
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Detergent Compositions (AREA)
- Medicinal Preparation (AREA)
- Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
Abstract
Aliphatic sulphonamides, which are stated to be useful as emulsifying agents, are prepared by condensing aliphatic sulphochlorides, the carbon chain of which may contain substituents or be interrupted by an atom or group of atoms such as O, S, SS, COO, CO NH or SO2 NH, with ammonia or an amine which contains one or two amino groups and may contain hydrophile groups, but must be free from hydroxy groups linked to an aliphatic radicle. Hydrophile groups are NH2, OH, SO2NH2, OSO4H, SO3H and COOH groups. In examples: (1) dodecylsulpho-chloride is condensed with ammonia or ethylenediamine; with ammonia, products are obtained which may be used in pastes, creams and ointments; (2) dodecylsulphochloride is condensed with methyltaurine and glycocoll; (3) tetradecylsulphochloride is condensed with sulphanilic acid or other aromatic amino sulphonic acids, e.g. of the naphthalene series. An aliphatic sulphochloride having the formula C17H35CO.NCH3C2H4SO2Ce is mentioned as an example of a starting material having an interrupted carbon chain. The Specification as open to inspection under Sect. 91 comprises also the condensation of the aliphatic sulphochlorides with polyamines and with hydrazine to give similar products. In an additional example, tetradecylsulphochloride is condensed with leucine, and stearyl sulphochloride with alanine or albumen decomposition products. The formates of the products are mentioned. This subject-matter does not appear in the Specification as accepted.ALSO:Aliphatic sulphonamides which are stated to be useful as wetting, emulsifying, cleansing and softening agents, e.g., in the manufacture and treatment of fabrics, leather and paper are prepared by condensing aliphatic sulphochlorides, the carbon chain of which may contain substituents or be interrupted by an atom or group of atoms such as O, S, SS, COO, CO NH or SO2 NH, with ammonia or an amine which contains one or two amino groups and may contain hydrophile groups but must be free from hydroxy groups linked to an aliphatic radicle. Hydrophile groups are NH2, OH, SO2NH2, OSO4H, SO3H and COOH groups. The formation of the sulphonamides as a step in the production of dyestuffs, cf. Specification 393,966, or of condensation products containing a chain of at least six ethenoxy groups, cf. Specification 380,851, is disclaimed. In examples: (1) dodecylsulpho-chloride is condensed with ammonia or ethylenediamine; with ammonia, products are obtained which may be used in pastes, creams and ointments; (2) dodecylsulphochloride is condensed in ether with methyltaurine and glycocoll; (3) tetradecylsulphochloride is condensed with sulphanilic acid or other aromatic amino sulphonic acids, e.g. of the naphthalene series. An aliphatic sulphochloride having the formula C17H35CO.NCH3.C2H4SO2Cl is mentioned as an example of a starting material having an interrupted carbon chain. The Specification as open to inspection under Sect. 91 comprises also the condensation of the aliphatic sulphochlorides with polyamines and with hydrazine. In an additional example, tetradecylsulphochloride is condensed with leucine, and stearyl sulphochloride with alanine or albumen decomposition products. The formates of the products are mentioned. This subject-matter does not appear in the Specification as accepted.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE413457X | 1932-04-20 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB413457A true GB413457A (en) | 1934-07-19 |
Family
ID=6442987
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB11568/33A Expired GB413457A (en) | 1932-04-20 | 1933-04-20 | Manufacture of emulsifying, cleansing, wetting or softening agents |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB413457A (en) |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE747667C (en) * | 1935-12-15 | 1944-10-09 | Process for the production of water-soluble, fat-free, high-molecular products | |
DE751132C (en) * | 1938-08-09 | 1952-11-10 | Ig Farbenindustrie Ag | Process for the preparation of water-soluble sulfonamide pellets |
DE767071C (en) * | 1939-01-28 | 1952-11-17 | Ig Farbenindustrie Ag | Process for the manufacture of condensation products |
DE884644C (en) * | 1938-11-19 | 1953-07-27 | Basf Ag | Process for the production of water-soluble capillary-active substances with particularly excellent foaming, wetting and washing effects |
DE767853C (en) * | 1938-09-17 | 1954-03-08 | Ig Farbenindustrie Ag | Process for the preparation of sulfamido compounds |
US2692237A (en) * | 1951-03-14 | 1954-10-19 | Colgate Palmolive Co | Detergent compositions |
US4476034A (en) * | 1981-06-27 | 1984-10-09 | Hoechst Aktiengesellschaft | Emulsifiers for metal processing oils |
-
1933
- 1933-04-20 GB GB11568/33A patent/GB413457A/en not_active Expired
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE747667C (en) * | 1935-12-15 | 1944-10-09 | Process for the production of water-soluble, fat-free, high-molecular products | |
DE751132C (en) * | 1938-08-09 | 1952-11-10 | Ig Farbenindustrie Ag | Process for the preparation of water-soluble sulfonamide pellets |
DE767853C (en) * | 1938-09-17 | 1954-03-08 | Ig Farbenindustrie Ag | Process for the preparation of sulfamido compounds |
DE884644C (en) * | 1938-11-19 | 1953-07-27 | Basf Ag | Process for the production of water-soluble capillary-active substances with particularly excellent foaming, wetting and washing effects |
DE767071C (en) * | 1939-01-28 | 1952-11-17 | Ig Farbenindustrie Ag | Process for the manufacture of condensation products |
US2692237A (en) * | 1951-03-14 | 1954-10-19 | Colgate Palmolive Co | Detergent compositions |
US4476034A (en) * | 1981-06-27 | 1984-10-09 | Hoechst Aktiengesellschaft | Emulsifiers for metal processing oils |
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