GB1027481A - Crystalline mixtures of capillary active salts and processes for preparing same - Google Patents
Crystalline mixtures of capillary active salts and processes for preparing sameInfo
- Publication number
- GB1027481A GB1027481A GB3692362A GB3692362A GB1027481A GB 1027481 A GB1027481 A GB 1027481A GB 3692362 A GB3692362 A GB 3692362A GB 3692362 A GB3692362 A GB 3692362A GB 1027481 A GB1027481 A GB 1027481A
- Authority
- GB
- United Kingdom
- Prior art keywords
- alcohol
- c2h4o
- formula
- processes
- mixture
- 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
- C07C59/00—Compounds having carboxyl groups bound to acyclic carbon atoms and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups
- C07C59/125—Saturated compounds having only one carboxyl group and containing ether groups, groups, groups, or groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
A mixture of salts of formula RO(C2H4O)nCH2COOM where R is C8- 14 alkylene, M is a cation and n is 1-5 is prepared either by treating a polyether mixture of general formula RO(C2H4O)nH (A) with chloroacetic acid or oxidizing a polyether mixture of formula RO(C2H4O)n+1H (B) and neutralizing the acid so produced. (A) and (B) may be prepared from an alcohol having 8-14 carbon atoms, e.g. lauryl alcohol, and 2-3 moles of ethylene oxide. The oxyethylated product may be fractionally distilled optionally under reduced pressure to remove any unchanged alcohol and products in which n is greater than 5. The unchanged alcohol may be reused. M may be an alkali metal. The product may be recrystallized from ethanol. In the examples the following alcohols are disclosed: lauryl alcohol containing 30% myristyl alcohol, decyl alcohol, dodecyl alcohol and dodecyl alcohol containing 30% myristyl alcohol. After treatment with ethylene oxide, distillation and treatment with chloroacetic acid, these are acidified with HCl and neutralized with NaOH, KOH or NH4OH.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB3692362A GB1027481A (en) | 1962-09-28 | 1962-09-28 | Crystalline mixtures of capillary active salts and processes for preparing same |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB3692362A GB1027481A (en) | 1962-09-28 | 1962-09-28 | Crystalline mixtures of capillary active salts and processes for preparing same |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1027481A true GB1027481A (en) | 1966-04-27 |
Family
ID=10392274
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB3692362A Expired GB1027481A (en) | 1962-09-28 | 1962-09-28 | Crystalline mixtures of capillary active salts and processes for preparing same |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB1027481A (en) |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4421930A (en) * | 1980-08-26 | 1983-12-20 | Chem-Y Fabriek Van Chemische Produkten B.V. | Process for preparing a pumpable surface-active product based on polyester acetic acid |
GB2148910A (en) * | 1983-10-28 | 1985-06-05 | Chevron Res | Stable emulsifier for substituted succinic anhydride compositions |
EP0217581A1 (en) * | 1985-09-16 | 1987-04-08 | Hercules Incorporated | Carboxylate salt compound and method for flavouring foodstuffs and tobacco |
US4759931A (en) * | 1983-04-20 | 1988-07-26 | 501 Stamicarbon B.V. | Novel liquid iodophors |
US5230823A (en) * | 1989-05-22 | 1993-07-27 | The Procter & Gamble Company | Light-duty liquid or gel dishwashing detergent composition containing an alkyl ethoxy carboxylate surfactant |
US5376310A (en) * | 1990-11-16 | 1994-12-27 | The Procter & Gamble Co. | Alkaline light duty dishwashing detergent composition containing an alkyl ethoxy carboxylate surfactant, magnesium ions, chelator and buffer |
US5378409A (en) * | 1990-11-16 | 1995-01-03 | The Procter & Gamble Co. | Light duty dishwashing detergent composition containing an alkyl ethoxy carboxylate surfactant and ions |
-
1962
- 1962-09-28 GB GB3692362A patent/GB1027481A/en not_active Expired
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4421930A (en) * | 1980-08-26 | 1983-12-20 | Chem-Y Fabriek Van Chemische Produkten B.V. | Process for preparing a pumpable surface-active product based on polyester acetic acid |
US4759931A (en) * | 1983-04-20 | 1988-07-26 | 501 Stamicarbon B.V. | Novel liquid iodophors |
GB2148910A (en) * | 1983-10-28 | 1985-06-05 | Chevron Res | Stable emulsifier for substituted succinic anhydride compositions |
EP0217581A1 (en) * | 1985-09-16 | 1987-04-08 | Hercules Incorporated | Carboxylate salt compound and method for flavouring foodstuffs and tobacco |
US5230823A (en) * | 1989-05-22 | 1993-07-27 | The Procter & Gamble Company | Light-duty liquid or gel dishwashing detergent composition containing an alkyl ethoxy carboxylate surfactant |
US5376310A (en) * | 1990-11-16 | 1994-12-27 | The Procter & Gamble Co. | Alkaline light duty dishwashing detergent composition containing an alkyl ethoxy carboxylate surfactant, magnesium ions, chelator and buffer |
US5378409A (en) * | 1990-11-16 | 1995-01-03 | The Procter & Gamble Co. | Light duty dishwashing detergent composition containing an alkyl ethoxy carboxylate surfactant and ions |
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