DE1016251B - Process for the preparation of monomagnesium dicalcium citrate for the treatment of pulmonary tuberculosis - Google Patents
Process for the preparation of monomagnesium dicalcium citrate for the treatment of pulmonary tuberculosisInfo
- Publication number
- DE1016251B DE1016251B DEO4076A DEO0004076A DE1016251B DE 1016251 B DE1016251 B DE 1016251B DE O4076 A DEO4076 A DE O4076A DE O0004076 A DEO0004076 A DE O0004076A DE 1016251 B DE1016251 B DE 1016251B
- Authority
- DE
- Germany
- Prior art keywords
- citrate
- monomagnesium
- treatment
- pulmonary tuberculosis
- magnesium
- 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.)
- Pending
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/41—Preparation of salts of carboxylic acids
- C07C51/418—Preparation of metal complexes containing carboxylic acid moieties
Description
Verfahren zur Herstellung von zur Behandlung der Lungentuberkulose dienendem Monomagnesiumdicalciumcitrat Die Erfindung betrifft die Herstellung von Monomagncsium-dicalciumcitrat der Zusammensetzung Ca2 Mg (C6 H5 07)2.Process for the preparation of for the treatment of pulmonary tuberculosis Serving Monomagnesium Dicalcium Citrate The invention relates to the production of Monomagncsium dicalcium citrate with the composition Ca2 Mg (C6 H5 07) 2.
Es wurde gefunden, daß das bisher nicht beschriebeine Monomagnesium-dicalciumcitrat eine günstige Wirkung bei der Behandlung der Lungentuberkulose besitzt. Dies Produkt fördert in besonders guter Weise den Verkalkungsprozeß bzw. die Verkapselung bei der Lungentuberkulose. Der Krankheitsverlauf wird dadurch in vielen Fällen günstig beeinflußt. It has been found that the hitherto not described is a monomagnesium dicalcium citrate has a beneficial effect in the treatment of pulmonary tuberculosis. This product promotes the calcification process or encapsulation in a particularly good way pulmonary tuberculosis. The course of the disease is thereby favorable in many cases influenced.
Die neue Verbindung kann erhalten werden, indem Citrenensäure mit für die Bildung des Monomagnesium - dicalciumcitrates berechneten Mengen von zur Bildung des Salzes befähigten Magnesium- und Calcium-Ausgangsprodukten umgesetzt wird. Die Umsetzung erfolgt zweckmäßig in wäßriger Lösung. Als Magnesium-Ausgangsprodukte können Magnesiummetall oder Magnesiumverbindungen, wie Magnesiumhydroxyd, -citrat, -carbonat, -formiat, -acetat, -lactat, verwendet werden. Entsprechendes gilt für die Calcium-Ausgangsprodukte. Auf 2 Mol Citronensäure ist bzw. sind 1-Grammatom Magnesium oder 1 Mol des Magnesium- und 2 Mol des Calcium-Ausgangsproduktes einzusetzen. The new compound can be obtained by using citrenic acid for the formation of the monomagnesium - dicalcium citrates calculated amounts of for Formation of the salt enabled magnesium and calcium starting products implemented will. The reaction is expediently carried out in aqueous solution. As magnesium raw materials magnesium metal or magnesium compounds such as magnesium hydroxide, citrate, carbonate, formate, acetate, lactate can be used. The same applies to the calcium starting products. There is or are 1 gram atom per 2 moles of citric acid Magnesium or 1 mol of the magnesium and 2 mol of the calcium starting product to be used.
Beispiel 1 2 Mol Citronensäure oder ein Vielfaches davon werden bzw. wird in etwa 1500 ccm Wasser gelöst. Example 1 2 moles of citric acid or a multiple thereof are or is dissolved in about 1500 ccm of water.
Nunmehr wird 1 Grammatom Magnesium in der Lösung aufgelöst. Hierbei scheidet sich saures Magnesiumcitrat ab. Durch Umsetzung mit 2 Mol Calciumcarbonat wird unter Kohlensäureentwicklung das Monomagnesium-dicalciumcitrat gebildet. Das Wasser wird durch Erhitzen bis auf 2000 abdestilliert, wonach ein trockenes Kristallpulver zurückbleibt. Die Ausbeute an Ca2Mg(C6H5O7)2 beträgt 95 0/o der Theorie.1 gram atom of magnesium is now dissolved in the solution. Here acidic magnesium citrate is deposited. By reaction with 2 moles of calcium carbonate Monomagnesium dicalcium citrate is formed with the evolution of carbonic acid. That Water is distilled off by heating up to 2000, after which a dry crystal powder remains behind. The yield of Ca2Mg (C6H5O7) 2 is 95% of theory.
Analyse Berechnet . . C 29,81 0/o, H 2,07 O/o; Gefunden . . C 29,50%, H 2,130/o.Analysis calculated. . C 29.81 O / o, H 2.07 O / o; Found . . C 29.50%, H 2.130 / o.
Beispiel 2 2 Mol Citronensäure oder ein Vielfaches davon werden bzw. wird in etwa 1500 ccm destilliertem Wasser gelöst. Nunmehr wird 1 Mol Magnesiumhydroxyd in der Lösung aufgelöst. Es bildet sich saures Magnesiumcitrat. Hierauf wird die Lösung mit 2 Mol Calciumcarbonat versetzt, wobei sich unter Kohlensäureentwicklung Monomagnesium- dicalciumcitrat bildet. Example 2 2 moles of citric acid or a multiple thereof are or are is dissolved in about 1500 cc of distilled water. Now 1 mole of magnesium hydroxide becomes dissolved in the solution. Acid magnesium citrate is formed. Then the Solution mixed with 2 mol of calcium carbonate, with evolution of carbonic acid Forms monomagnesium dicalcium citrate.
Das Wasser wird durch Erhitzen bis auf 2000 abdestilliert, wonach ein trockenes Kristallpulver zurückbleibt. Die Ausbeute an Ca2 Mg (C6 H5 07)2 beträgt 95% der Theorie.The water is distilled off by heating up to 2000, after which a dry crystal powder remains. The yield of Ca2 Mg (C6 H5 07) 2 is 95% of theory.
Analyse Berechnet.. C 29,81 0/0, H 2,07 0/o; Gefunden .. C 29,40O/o, H 1,990/o.Analysis Calculated. C 29.81%, H 2.07%; Found .. C 29.40O / o, H 1.990 / o.
Claims (1)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DEO4076A DE1016251B (en) | 1955-01-22 | 1955-01-22 | Process for the preparation of monomagnesium dicalcium citrate for the treatment of pulmonary tuberculosis |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DEO4076A DE1016251B (en) | 1955-01-22 | 1955-01-22 | Process for the preparation of monomagnesium dicalcium citrate for the treatment of pulmonary tuberculosis |
Publications (1)
Publication Number | Publication Date |
---|---|
DE1016251B true DE1016251B (en) | 1957-09-26 |
Family
ID=7350261
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DEO4076A Pending DE1016251B (en) | 1955-01-22 | 1955-01-22 | Process for the preparation of monomagnesium dicalcium citrate for the treatment of pulmonary tuberculosis |
Country Status (1)
Country | Link |
---|---|
DE (1) | DE1016251B (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2394513A1 (en) * | 1977-06-16 | 1979-01-12 | Madaus & Co Dr | NEW ALKALINE ACID CITRATE, PROCESS FOR ITS PREPARATION AND USE AS A MEDICINAL PRODUCT |
EP0380829A1 (en) * | 1988-01-05 | 1990-08-08 | Mission Pharmacal Company, Inc. | Magnesium potassium citrate |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE857363C (en) * | 1949-09-13 | 1952-11-27 | Johann G W Opfermann & Sohn | Process for the production of ferrocalcium citrate |
DE869485C (en) * | 1942-12-29 | 1953-03-05 | Basf Ag | Process for the production of aliphatic alcohols with more than 2 carbon atoms or their sulfuric acid esters |
DE874305C (en) * | 1950-11-22 | 1953-04-23 | Johann G W Opfermann & Sohn | Process for the production of ferrocalcium citrate |
DE882699C (en) * | 1950-04-09 | 1953-07-09 | Wilhelm Theopold Dr Med | Process for the production of calcium-citric acid complex compounds or their aqueous solutions |
-
1955
- 1955-01-22 DE DEO4076A patent/DE1016251B/en active Pending
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE869485C (en) * | 1942-12-29 | 1953-03-05 | Basf Ag | Process for the production of aliphatic alcohols with more than 2 carbon atoms or their sulfuric acid esters |
DE857363C (en) * | 1949-09-13 | 1952-11-27 | Johann G W Opfermann & Sohn | Process for the production of ferrocalcium citrate |
DE882699C (en) * | 1950-04-09 | 1953-07-09 | Wilhelm Theopold Dr Med | Process for the production of calcium-citric acid complex compounds or their aqueous solutions |
DE874305C (en) * | 1950-11-22 | 1953-04-23 | Johann G W Opfermann & Sohn | Process for the production of ferrocalcium citrate |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2394513A1 (en) * | 1977-06-16 | 1979-01-12 | Madaus & Co Dr | NEW ALKALINE ACID CITRATE, PROCESS FOR ITS PREPARATION AND USE AS A MEDICINAL PRODUCT |
EP0380829A1 (en) * | 1988-01-05 | 1990-08-08 | Mission Pharmacal Company, Inc. | Magnesium potassium citrate |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
DE1016251B (en) | Process for the preparation of monomagnesium dicalcium citrate for the treatment of pulmonary tuberculosis | |
DE1468344C3 (en) | Methylthio-chloro-cinnamic acids and process for their preparation | |
DE741320C (en) | Process for the preparation of 2, 4, 6-trimethyl-3-acetylpyridine | |
DE945926C (en) | Process for the production of ªŠ-acetyl-lysine | |
DE710225C (en) | Process for the preparation of compounds of dioxydialkylstilbenes | |
DE646932C (en) | Process for the production of diamino alcohols of the fatty aromatic series | |
DE494320C (en) | Process for the preparation of isopropyl-n-butylmalonic ester | |
DE920077C (en) | Process for the preparation of derivatives of p-aminosalicylic acid | |
DE527713C (en) | Process for the preparation of a compound from chloral and p-phenetidine | |
DE806453C (en) | Process for the production of dry, non-hygroscopic double salts from calcium salts of aliphatic carboxylic acids and calcium chloride | |
DE806458C (en) | Process for the production of coumarins | |
DE938614C (en) | Process for the production of methyltrimethylolmethane | |
DE848502C (en) | Process for the preparation of derivatives of dihydrosafole | |
DE641994C (en) | Process for the preparation of acyl derivatives of the dihydrofollicle hormone | |
DE672372C (en) | Process for the preparation of ª ‰ - (p-Oxyphenyl) -isopropylmethylamine | |
DE859790C (en) | Process for increasing the solubility of sulfonamides | |
DE953879C (en) | Process for the preparation of pyrone (4) | |
DE848043C (en) | Process for the preparation of formyl compounds of 2,6-dioxy-4,5-diaminopyrimidine and its methyl derivatives | |
DE844300C (en) | Process for the preparation of 5-nitro-uracil-carboxylic acid (4) or derivatives thereof substituted on the nitrogen atom | |
DE246207C (en) | ||
DE854956C (en) | Method of making a pteridine bead | |
DE924821C (en) | Process for the production of therapeutically valuable salts | |
DE1135910B (en) | Process for the preparation of 2,5-bis-methylaethyleneimino-hydroquinone | |
DE942865C (en) | Process for the preparation of 2-methyl-4-chlorophenoxyacetic acid calcium and / or 2-methyl-6-chlorophenoxyacetic acid calcium | |
DE233437C (en) |