GB541682A - Improvements in fatty acid amide derivatives - Google Patents
Improvements in fatty acid amide derivativesInfo
- Publication number
- GB541682A GB541682A GB3625/40A GB362540A GB541682A GB 541682 A GB541682 A GB 541682A GB 3625/40 A GB3625/40 A GB 3625/40A GB 362540 A GB362540 A GB 362540A GB 541682 A GB541682 A GB 541682A
- Authority
- GB
- United Kingdom
- Prior art keywords
- condensed
- product
- oil
- acted
- fatty 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
Links
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/40—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
- A61K8/42—Amides
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q5/00—Preparations for care of the hair
- A61Q5/02—Preparations for cleaning the hair
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Birds (AREA)
- Epidemiology (AREA)
- Emulsifying, Dispersing, Foam-Producing Or Wetting Agents (AREA)
Abstract
541,682. Acid amide derivatives. ALFRAMINE CORPORATION. Feb. 27, 1940, No. 3625. Convention date, March 1, 1939. Samples furnished. [Classes 2 (iii) and 15 (ii)] [Also in Group VI] Aliphatic aldehydes containing one to five carbon atoms are condensed with fatty acid alkylolamides having the formula R.CO- (NHC 2 H 4 )nNHCyH 2y OH in which R is an aliphatic chain having at least 7 carbon atoms, y is a number from 2 to 4 and n a number 0 to 3. The fatty acid alkylolamides may be derived from fatty acids or esters such as sperm oil, cod liver oil and hardened cod liver oil by condensation with the appropriate alkylolamine or the fatty acid or ester may be condensed with ammonia and then re-acted with alkyleneoxides or chlorhydrins. Butyraldehyde and exotonaldehyde may be used for re-action with the alkylolamides. The products, by sulphonation are converted into soluble wetting, washing and foaming agents. They may be used in fire extinguishers and in shampoos. The unneutralized sulphonic acids are suitable for breaking oil emulsions of fatty acids, fats and mineral oils. In examples : (1) monoethanolamine is condensed with castor oil and coconut oil, the products condensed with formaldehyde and then sulphonated : (2) castor oil is condensed with hydroxyethylethylenediamine or hydroxypropylethylenediamine, the product re-acted with formaldehyde and sulphonated : (3) castor oil is condensed with monoethanolamine, the product re-acted with acetaldehyde and sulphonated : (4) olive oil is condensed with isobutanolamine, the product re-acted with formaldehyde and sulphonated: (5) palm oil fatty acid is condensed with hydroxyethylethylenediamine and the product re-acted with formaldehyde : (6) the product of example 5, dissolved in acetic acid is used in neutral or acid dyebaths, containing sulphates to secure full dye penetration : (7) the unsulphonated product from example 2 is used in carbonizing wool, the latter retains its capacity to absorb dyes. The Specification as open to inspection under Sect. 91 comprises also the use of fatty acid alkylolamides having the formula R.CO- (NHCx H 2x )nNHO y H 2y OH wherein R and n are as above defined and x and y are a number from 2 to 5. In a further example, viscose crepe containing titanium oxide is softened by treatment in a bath containing the product of example 5 and lactic acid followed by calendering. In another example, tallow is re-acted with hydroxypropylethylenediamine and acetaldehyde, and the product is used together with lactic acid in a bath for the treatment of acetate artificial silk. This subject-matter does not appear in the Specification as accepted.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US541682XA | 1939-03-01 | 1939-03-01 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB541682A true GB541682A (en) | 1941-12-08 |
Family
ID=21989187
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB3625/40A Expired GB541682A (en) | 1939-03-01 | 1940-02-27 | Improvements in fatty acid amide derivatives |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB541682A (en) |
-
1940
- 1940-02-27 GB GB3625/40A patent/GB541682A/en not_active Expired
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