AT48348B - Process for preparing concentrated solutions of thiosinamine. - Google Patents
Process for preparing concentrated solutions of thiosinamine.Info
- Publication number
- AT48348B AT48348B AT48348DA AT48348B AT 48348 B AT48348 B AT 48348B AT 48348D A AT48348D A AT 48348DA AT 48348 B AT48348 B AT 48348B
- Authority
- AT
- Austria
- Prior art keywords
- thiosinamine
- concentrated solutions
- preparing concentrated
- sodium
- salicylic acid
- Prior art date
Links
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
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Verfahren zur Darstellung konzentrierter Lösungen von Thiosinamin.
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ausscheidet, so dass ein öfteres, mit Zerseztung verbundenes Anwärmen nicht notwendig ist.
Bekanntlich haben viele Personen eine erhebliche Idiosynkrasie gegen Salizylsäure und Salizylsäurepräparate, und es schien daher angebracht, nach Kombination enzu suchen, die, ohne Salizylsäure zu enthalten, alle Vorteile der mittels salizytsaurem Natriums erhältlichen Thiosinaminlösung aufweisen. Bei diesen Untersuchungen wurde nun die überraschende Fest-
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Es sind dies alle diejenigen Substanzen, die gleichzeitig bis zu einem gewissen Grade sauren und basischen Charakter besitzen. ohne dass der eine oder andere erheblich vorwiegt, also Salze von schwächeren Säuren mit Alkalien, Aminokörper mit sauren Gruppen, wie Aminosäuren, Amilocster und ähnliche Substanzen.
Besonders haben sich die folgenden Zusätze bewährt : Natriumbiborat, Natriumbenzoat. zimmtsaures Natrium. Glykokell. Urethan und dergleichen. Das Verfahren soll an folgenden Beispielen erläutert werden.
Beispiel l : 1 Mol. Thiosinamin und @@ Mol. Natriumbiborat werden in Wasser gelöst
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Gefäss auf 80 erhitzt. Die entstandene Schmelze wird beim Erkalten fest und ist in Wasser sehr leicht löslich.
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Process for preparing concentrated solutions of thiosinamine.
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separates, so that frequent heating associated with decomposition is not necessary.
It is known that many people have considerable idiosyncrasy against salicylic acid and salicylic acid preparations and it therefore seemed appropriate to look for combinations which, without containing salicylic acid, would have all the advantages of the thiosinamine solution obtainable with sodium salicylic acid. In these investigations, the surprising festival
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These are all those substances which, to a certain extent, have both an acidic and a basic character. without one or the other being predominant, i.e. salts of weaker acids with alkalis, amino bodies with acidic groups such as amino acids, amilocsters and similar substances.
The following additives have proven particularly useful: sodium borate, sodium benzoate. cinnamic acid sodium. Glycocell. Urethane and the like. The following examples illustrate the process.
Example 1: 1 mol. Thiosinamine and @@ mol. Sodium biborate are dissolved in water
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Vessel heated to 80. The resulting melt solidifies on cooling and is very easily soluble in water.
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Claims (1)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE1904163804D DE163804C (en) | 1904-12-12 | ||
| DE48348X | 1909-02-26 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AT48348B true AT48348B (en) | 1911-06-10 |
Family
ID=25749064
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AT48348D AT48348B (en) | 1904-12-12 | 1909-11-10 | Process for preparing concentrated solutions of thiosinamine. |
Country Status (1)
| Country | Link |
|---|---|
| AT (1) | AT48348B (en) |
-
1909
- 1909-11-10 AT AT48348D patent/AT48348B/en active
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