GB401481A - A process for the treatment of tanned or non-tanned animal hides - Google Patents
A process for the treatment of tanned or non-tanned animal hidesInfo
- Publication number
- GB401481A GB401481A GB27426/32A GB2742632A GB401481A GB 401481 A GB401481 A GB 401481A GB 27426/32 A GB27426/32 A GB 27426/32A GB 2742632 A GB2742632 A GB 2742632A GB 401481 A GB401481 A GB 401481A
- Authority
- GB
- United Kingdom
- Prior art keywords
- acid
- aliphatic radical
- cresoxyl
- aralkyl
- aryl
- 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
- C14—SKINS; HIDES; PELTS; LEATHER
- C14C—CHEMICAL TREATMENT OF HIDES, SKINS OR LEATHER, e.g. TANNING, IMPREGNATING, FINISHING; APPARATUS THEREFOR; COMPOSITIONS FOR TANNING
- C14C9/00—Impregnating leather for preserving, waterproofing, making resistant to heat or similar purposes
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
- Investigating Or Analysing Biological Materials (AREA)
Abstract
Products having the formula RCOXR1SO3Z in which R is an aliphatic radical having more than one double bond and more than eight carbon atoms, X is O, NH, N-alkyl, N-aralkyl or N-aryl, R1 an aliphatic radical and Z an alkali metal, ammonium or hydrogen, are stated to be emulsifying agents. They readily emulsify oils and fats with or without the use of soap. In examples, the reaction product of the fatty acid chloride of train oil with hydroxyethane sulphonic acid or with aminoethanesulphonic acid is employed. The action of the fatty acid amides is increased by introducing a methyl, ethyl or benzyl group. The Specification as open to inspection under Sect. 91 comprises also the use of compounds having the formula RXR1SO3Z in which R1 and Z are as defined above, R is any aliphatic radical containing more than eight carbon atoms and X is O, S, OCOO, COO, NY, CONY, OCONY or YNCONY, Y being hydrogen, alkyl, aralkyl or aryl. In further examples, b - cresoxyl - a - oleyl - hydroxypropanesulphonic acid, the sodium salt of oleylmethylamino ethanesulphonic acid, oleylhydroxyethanesulphonic acid, oleylaminoethanesulphonic acid and the products obtained by condensing sodium b - cresoxyl - a - oleylhydroxypropanesulphonate with formaldehyde, and chlorcarbonicdodecyl ester with hydroxyethanesulphonic acid or with amino- or methylaminoethanesulphonic acid are employed. Palmitylhydroxyethanesulphonic acid is also mentioned. This subject-matter does not appear in the Specification as accepted.ALSO:Products having the formula RCOXR1SO3Z in which R is an aliphatic radical having more than one double bond and more than eight carbon atoms, X is O, NH, N-alkyl, N-aralkyl or N-aryl, R1 an aliphatic radical and Z an alkali metal, ammonium or hydrogen, are stated to be tanning, greasing and penetrating agents. They may be added to dyebaths for dyeing leather, e.g. in topping with basic dyestuffs. In examples, the reaction product of the fatty acid chloride of train oil with hydroxyethane sulphonic acid or with aminoethanesulphonic acid is employed. The action of the fatty acid amides is increased by introducing a methyl, ethyl or benzyl group. The Specification as open to inspection under Sect. 91 comprises also the treatment of hides with compounds having the formula RXR1SO3Z in which R1 and Z are as defined above and R is any aliphatic radical containing more than eight carbon atoms and X is O, S, OCOO, CCO, NY, CONY, OCONY or YNCONY, Y being hydrogen, alkyl, aralkyl or aryl. In further examples, b -cresoxyl-a -oleyl-hydroxypropanesulphonic acid, the sodium salt of oleylmethyl-aminoethanesulphonic acid, oleylhydroxyethanesulphonic acid, oleylaminoethanesulphonic acid and the products obtained by condensing sodium b -cresoxyl-a -oleylhydroxy-propanesulphonate with formaldehyde and chlorcarbonicdodecyl ester with hydroxyethanesulphonic acid or with amino- or methylaminoethanesulphonic acid are employed. Palmitylhydroxyethanesulphonic acid is also mentioned. This subject-matter does not appear in the Specification as accepted.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE401481X | 1931-10-03 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB401481A true GB401481A (en) | 1933-11-16 |
Family
ID=6405990
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB27426/32A Expired GB401481A (en) | 1931-10-03 | 1932-10-03 | A process for the treatment of tanned or non-tanned animal hides |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB401481A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2192199A (en) * | 1986-07-04 | 1988-01-06 | Sandoz Ltd | Penetration dyeing of leather with basic dyes |
-
1932
- 1932-10-03 GB GB27426/32A patent/GB401481A/en not_active Expired
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2192199A (en) * | 1986-07-04 | 1988-01-06 | Sandoz Ltd | Penetration dyeing of leather with basic dyes |
FR2601050A1 (en) * | 1986-07-04 | 1988-01-08 | Sandoz Sa | SLICED DYEING PROCESS FOR TANNED LEATHER |
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