GB161859A - Improvements in the manufacture of certain naphthylamine sulphonic acids - Google Patents
Improvements in the manufacture of certain naphthylamine sulphonic acidsInfo
- Publication number
- GB161859A GB161859A GB1427620A GB1427620A GB161859A GB 161859 A GB161859 A GB 161859A GB 1427620 A GB1427620 A GB 1427620A GB 1427620 A GB1427620 A GB 1427620A GB 161859 A GB161859 A GB 161859A
- Authority
- GB
- United Kingdom
- Prior art keywords
- acid
- salts
- acids
- solution
- barium salt
- 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
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
1 :4 :8-Naphthylamine disulphonic acid is separated from the isomeric acids, principally the 1 :3 :8-acid, which accompany its production, by taking advantage of the relative insolubility of the normal barium salt in hot water. The 1 :3 :8-acid is then separated from the remaining acids by taking advantage of the sparing solubility in hot water of its acid barium salt. According to the process, a solution of a barium salt is added to a concentrated solution of the crude disodium salts of the acids resulting from the process of preparation described in Specification 4625/88, or a solution of the acids themselves is boiled with barium carbonate, oxide or hydroxide, whereby the normal barium salt of the 1 :4 :8-acid is precipitated. The filtrate is acidified, when the acid barium salt of the 1 :3 :8-acid is thrown down. The resulting barium salts can be converted into other salts by double decomposition. A preliminary purification of the solution of the crude disodium salts may be effected by adding acid to precipitate the acid sodium salts and then neutralizing these before treatment with the barium salt; or the acid sodium salts may be suspended in water, acid then added, and the solution boiled with barium carbonate for the separation treatment. The process may be applied to the purification of individual salts of the 1 :4 :8- and 1 :3 :8-acids.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB1427620A GB161859A (en) | 1920-05-25 | 1920-05-25 | Improvements in the manufacture of certain naphthylamine sulphonic acids |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB1427620A GB161859A (en) | 1920-05-25 | 1920-05-25 | Improvements in the manufacture of certain naphthylamine sulphonic acids |
Publications (1)
Publication Number | Publication Date |
---|---|
GB161859A true GB161859A (en) | 1921-04-21 |
Family
ID=10038225
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB1427620A Expired GB161859A (en) | 1920-05-25 | 1920-05-25 | Improvements in the manufacture of certain naphthylamine sulphonic acids |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB161859A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4338261A (en) | 1980-04-05 | 1982-07-06 | Bayer Aktiengesellschaft | Process for the preparation of 1-naphthylamine-4,6-disulphonic acid and 1-naphthylamine-2,4,6-trisulphonic acid |
-
1920
- 1920-05-25 GB GB1427620A patent/GB161859A/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4338261A (en) | 1980-04-05 | 1982-07-06 | Bayer Aktiengesellschaft | Process for the preparation of 1-naphthylamine-4,6-disulphonic acid and 1-naphthylamine-2,4,6-trisulphonic acid |
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