GB658766A - Improvements in and relating to the purification of antibiotics - Google Patents
Improvements in and relating to the purification of antibioticsInfo
- Publication number
- GB658766A GB658766A GB2353848A GB2353848A GB658766A GB 658766 A GB658766 A GB 658766A GB 2353848 A GB2353848 A GB 2353848A GB 2353848 A GB2353848 A GB 2353848A GB 658766 A GB658766 A GB 658766A
- Authority
- GB
- United Kingdom
- Prior art keywords
- polymyxin
- salt
- reacted
- ethanol
- solution
- 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
Abstract
Partially purified polymyxin is purified further by treating in solution the polymyxin as the free base or as a salt thereof with BETA-naphthalene sulphonic acid, separating the salt thus obtained, purifying the salt by recrystallization and recovering the polymyxin therefrom. The free polymyxin as its salt is reacted in aqueous medium, and as the free base is reacted in solution in an alcohol containing 2 to 5 carbon atoms. The recrystallized salt may be reacted with an acid to give the salt of polymyxin, or may be reacted with ammonia to liberate the polymyxin which may then be reacted with an acid to form the salt. The partially purified polymyxin is preferably obtained by the process of Specification 647,925. In examples: (1) polymyxin b -hydrochloride and b -naphthalene sulphonic acid are reacted in aqueous solution. The product, an oil, is dissolved in aqueous ethanol, and more ethanol then added till the solution is cloudy, when crystallization begins. After a charcoal treatment the crystallization is repeated. The crystals suspended in methanol or ethanol are then treated with concentrated sulphuric acid and polymyxin sulphate precipitates on dilution with water; (2) polymyxin B, liberated from its hydrochloride, b -naphthalene sulphonic acid and dry ethanol are mixed, water is then added until a clear solution is obtained, and more ethanol is then added to cause precipitation. The product is re-crystallized by dissolving in aqueous ethanol and then adding dry ethanol. Polymyxin is then obtained by adding aqueous ammonia, and is converted into its sulphate or hydrochloride.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2353848A GB658766A (en) | 1948-09-07 | 1948-09-07 | Improvements in and relating to the purification of antibiotics |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2353848A GB658766A (en) | 1948-09-07 | 1948-09-07 | Improvements in and relating to the purification of antibiotics |
Publications (1)
Publication Number | Publication Date |
---|---|
GB658766A true GB658766A (en) | 1951-10-10 |
Family
ID=10197247
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB2353848A Expired GB658766A (en) | 1948-09-07 | 1948-09-07 | Improvements in and relating to the purification of antibiotics |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB658766A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3413398A (en) * | 1963-08-30 | 1968-11-26 | Burroughs Wellcome Co | Purification of polymyxin |
WO2010058427A2 (en) | 2008-11-24 | 2010-05-27 | Reliance Life Sciences Pvt. Ltd. | Process for production and purification of polymyxin b sulfate |
-
1948
- 1948-09-07 GB GB2353848A patent/GB658766A/en not_active Expired
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3413398A (en) * | 1963-08-30 | 1968-11-26 | Burroughs Wellcome Co | Purification of polymyxin |
WO2010058427A2 (en) | 2008-11-24 | 2010-05-27 | Reliance Life Sciences Pvt. Ltd. | Process for production and purification of polymyxin b sulfate |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
GB658766A (en) | Improvements in and relating to the purification of antibiotics | |
GB579459A (en) | Process for the purification of 4-hydroxycoumarins | |
US2250332A (en) | Preparation of isocytosine | |
US2580195A (en) | Method of purifying 4-aminosalicylic acid | |
SU72375A1 (en) | The method of purification of 4-sulfoanthranilic acid | |
GB650341A (en) | Method for the production of amido sulphonic acid | |
GB686221A (en) | Improvements in the recovery of nickel from solutions | |
US2230970A (en) | Purification of crude isocytosine | |
GB331648A (en) | A process for the recovery of salts contained in the waste water of artificial silk factories | |
GB990120A (en) | Process for the purification of dehydrocholic acid | |
SU118212A1 (en) | Method of cleaning technical para-aminosalicylic acid | |
GB733268A (en) | Improvements in or relating to process for purification of tyrosine | |
GB626641A (en) | A process for the production and purification of common salt and other components from brine, including the dehydration of glauber salt | |
GB711307A (en) | Improvements in or relating to a new derivative of ª -pyridine aldehyde | |
KR940011456A (en) | Process for preparing high purity N (N)-(2-sulfatoethyl) piperazine | |
GB268158A (en) | Improvements in the separation and purification of vanillin | |
GB649743A (en) | Improvements in or relating to the manufacture of crystalline sodium penicillin | |
GB655649A (en) | Improvements in or relating to the purification of penicillin salts | |
GB703470A (en) | Process for the manufacture of hydrazine sulfate | |
GB672684A (en) | Improvements in or relating to organic amino acids | |
GB149095A (en) | Improvements in or relating to the manufacture of ammonium nitrate | |
GB945475A (en) | Method of producing pure neomycin and its salts | |
GB790279A (en) | Improvements in or relating to purification of amino compounds | |
GB669519A (en) | Production of hydrofluoric acid | |
GB219327A (en) | A process for separating hafnium and zirconium |