DE718991C - Process for the production of durable solutions of ascorbic acid salts of histidine - Google Patents

Process for the production of durable solutions of ascorbic acid salts of histidine

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Publication number
DE718991C
DE718991C DEH151953D DEH0151953D DE718991C DE 718991 C DE718991 C DE 718991C DE H151953 D DEH151953 D DE H151953D DE H0151953 D DEH0151953 D DE H0151953D DE 718991 C DE718991 C DE 718991C
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Germany
Prior art keywords
histidine
ascorbic acid
solutions
acid salts
production
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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
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DEH151953D
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German (de)
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F Hoffmann La Roche AG
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F Hoffmann La Roche AG
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Publication date
Application filed by F Hoffmann La Roche AG filed Critical F Hoffmann La Roche AG
Application granted granted Critical
Publication of DE718991C publication Critical patent/DE718991C/en
Expired legal-status Critical Current

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  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Food Preservation Except Freezing, Refrigeration, And Drying (AREA)

Description

Verfahren zur Herstellung haltbarer Lösungen von ascorbinsauren Salzen des Histidins Wenn man Ascorbinsäure mit Histidin neutralisiert, so sind die Lösamgen der enttehenden Salze nicht haltbar, was gchon daran zu erkennen ist, daß sie sich sehr bald lümbeerrot bis dunkelorangebraun färben. Löst man z. B. 3,I g Histidin (2/l00 Mol.) und I,76 g Ascorbinsäure (1/10o Mol.) ;:n roo ccm Wasser, so hat die entstehende Salzlösung ein p,3 von 6,o. Sie verfärbt sich in kürzester Zeit, zunächst hellrosa, dann himbeerrot, schließlich dunkelorangebraun. Lösungen von anderen ascorbinsauren Salzen, z. B. Natriumascorbat, oder anderen Histidinsalzen, z. B. Histidinhydrochlorid, von gleiehen pl, zeigen diese rasche" Verfärbung nicht, es isst dies eine besondere Eigenschaft der Lösungen von ascorbinsturen Salz. des Histidins. Die Konstitution der entstehenden gefärbten Verbindungen wurde noch nicht,ernhttelt.Process for the preparation of stable solutions of ascorbic acid salts des histidine. If ascorbic acid is neutralized with histidine, the solutions are the resulting salts are not durable, which can already be recognized by the fact that they are very soon it turns luberry-red to dark orange-brown. If you solve z. B. 3, I g histidine (2/100 mol.) And 1.76 g of ascorbic acid (1 / 10o mol.);: N roo ccm of water, so the resulting saline solution a p, 3 of 6, o. It'll change color in no time, at first light pink, then raspberry red, finally dark orange brown. Solutions of other ascorbic acids Salts, e.g. B. sodium ascorbate, or other histidine salts, e.g. B. histidine hydrochloride, von gleiehen pl, do not show this rapid "discoloration, it eats this a special one Property of solutions of ascorbic salt. of histidine. The constitution the resulting colored compounds have not yet been harvested.

Die Vexfärbung läßt sich nun vollständig verhindern, wenn man dafüir sorgt, daß wälirend der Herstellung der Lösungen der ascorbinsauren Salze des Histidins die Luft peinlich ferngehalten wird und auch die fertigen Lösungen vor Luftzutritt geschützt werden. Man herreicht dies z. B. dadurch, daß man Ascorbinsäure und Histidin oder Ascorbate und Salze des Histidins in den gewünschten Mengenverhältnissen in Wasser löst, durch welches z. B. längere Zeit Kohlensäure oder Stickstoff geleitet wurde, und daß man die fertigen Lösungen vor Luftzutritt bewahrt, indem man die Behälter mit einem sauerstofffreien Gase füllt oder die Luft daraus durch Evakuierung entfernt.Vex staining can now be completely prevented if one is for it ensures that during the preparation of the solutions of the ascorbic acid salts of histidine the air is embarrassingly kept away and also the finished solutions from air admission to be protected. One reaches this z. B. by using ascorbic acid and histidine or ascorbates and salts of histidine in the desired proportions Dissolves water through which z. B. passed for a long time carbonic acid or nitrogen was, and that the finished solutions are protected from the ingress of air by the Filling containers with an oxygen-free gas or removing the air from it by evacuation removed.

Das leben geschilderte Verfahren beruht auf der Erkenntnis, daß die Veränderung von ascorbinsauren. Salzen des Histidins in Gegenwart von Luft nicht wie bei anderen Salzen der Ascorbinsäure auf eine Oxydation der Ascorbinsäure, sondern auf eine Zersetzung des Histidins zurückzuführen ist. Die Zersetzung des Histidins ist bedingt durch die Gegenwart: von Ascorbinsäure. Sie tritt nicht ,ein bei Gegenwart von Luft, ohne Ascorbinsäure. Die getroffenen Maßnahmen dienen somit nicht dem Schutze der Ascorbinsäure, sondern zur Verhinderung der Zersetzung des Histidins. Beispiel i 3 i o Teile Histidin und i 7 6 Teile Ascorbinsäure werden unter konstantem Durchleiten von Stickstoff in 5ooo Teilen Wasser gelöst, welches vorher ausgekocht und unter Stickstoffdurchleitung abgekühlt worden war. Die fertige Lösung wird z. B. in mit Stickstoff gefüllte Ampullen abgefüllt, welche sogleich zugesclunolzen werden. Diese Lösungen bleiben dauernd farblos, ja sie können sogar im strömenden Dampfe erhitzt (sterf siert) werden, ohne daß eine merkliche Verfärbung auftritt.The process described in life is based on the knowledge that the Change of ascorbic acid. Do not salt the histidine in the presence of air as with other salts of ascorbic acid on an oxidation of the ascorbic acid, but is due to decomposition of the histidine. The decomposition of histidine is due to the presence: of ascorbic acid. She does not enter the present of air, without ascorbic acid. The measures taken are therefore not intended to protect you of ascorbic acid, but to prevent the decomposition of histidine. example i 3 i o parts of histidine and i 7 6 parts of ascorbic acid are passed through constantly dissolved by nitrogen in 5,000 parts of water, which was previously boiled and under Nitrogen bubbling had been cooled. The finished solution is z. Am with Nitrogen-filled ampoules are filled, which are immediately closed. These Solutions remain permanently colorless, and they can even be heated in flowing steam (Sterfized) without any noticeable discoloration.

Beispiel z 2o9,5 Teile Histidinmonohydrochlorid (+ i Kristallwasser) und i gg Teile Natriumascorbat werden in 5ooo Teilen sauerstofffreiem Wasser gelöst und während der Lösung Kohlensäure eingeleitet. Aus den Gefäßen, in welchen die Lösung aufbewahrt werden soll, wird die Luft durch Evakuierung entfernt. Die Lösungen bleiben farblos.Example z 2o9.5 parts of histidine monohydrochloride (+ i water of crystallization) and i gg parts of sodium ascorbate are dissolved in 500 parts of oxygen-free water and carbonic acid introduced during the dissolution. From the vessels in which the If the solution is to be stored, the air is removed by evacuation. The solutions remain colorless.

Claims (1)

PATI:NTA\SPRUCii: Verfahren zur Herstellung haltbarer Lösungen von ascorbinsauren Salzen des Histidins, dadurch gekennzeichnet, dap, wässerige Lösungen dieser Salze zur Verhinderung der Zersetzung des Histidins mit sauersitofffreien Gasen gesättigt und in mit diesen Gasen gefüllten oder evakuierten Behältern aufbewahrt werden.PATI: NTA \ SPRUCii: Process for making durable solutions of ascorbic acid salts of histidine, characterized in dap, aqueous solutions these salts to prevent the decomposition of the histidine with oxygen-free Saturated gases and stored in containers filled with these gases or evacuated will.
DEH151953D 1936-07-09 1937-06-11 Process for the production of durable solutions of ascorbic acid salts of histidine Expired DE718991C (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CH718991X 1936-07-09

Publications (1)

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DE718991C true DE718991C (en) 1942-03-26

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DEH151953D Expired DE718991C (en) 1936-07-09 1937-06-11 Process for the production of durable solutions of ascorbic acid salts of histidine

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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1012607B (en) * 1954-06-19 1957-07-25 Hans Meyer Doering Dr Med Process for the preparation of water-soluble therapeutic agents with bactericidal to bacteriostatic effects

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1012607B (en) * 1954-06-19 1957-07-25 Hans Meyer Doering Dr Med Process for the preparation of water-soluble therapeutic agents with bactericidal to bacteriostatic effects

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