CH124948A - Process for producing a soluble manganese compound. - Google Patents
Process for producing a soluble manganese compound.Info
- Publication number
- CH124948A CH124948A CH124948DA CH124948A CH 124948 A CH124948 A CH 124948A CH 124948D A CH124948D A CH 124948DA CH 124948 A CH124948 A CH 124948A
- Authority
- CH
- Switzerland
- Prior art keywords
- manganese compound
- producing
- soluble manganese
- soluble
- compound
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims description 5
- 150000002697 manganese compounds Chemical class 0.000 title claims description 3
- 229940093474 manganese carbonate Drugs 0.000 claims description 3
- 235000006748 manganese carbonate Nutrition 0.000 claims description 3
- 239000011656 manganese carbonate Substances 0.000 claims description 3
- 229910000016 manganese(II) carbonate Inorganic materials 0.000 claims description 3
- XMWCXZJXESXBBY-UHFFFAOYSA-L manganese(ii) carbonate Chemical compound [Mn+2].[O-]C([O-])=O XMWCXZJXESXBBY-UHFFFAOYSA-L 0.000 claims description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 3
- 208000035473 Communicable disease Diseases 0.000 claims description 2
- UGECXIBKSDDQDH-UHFFFAOYSA-L disodium;3,4-dihydroxybenzene-1,2-disulfonate Chemical compound [Na+].[Na+].OC1=CC=C(S([O-])(=O)=O)C(S([O-])(=O)=O)=C1O UGECXIBKSDDQDH-UHFFFAOYSA-L 0.000 claims description 2
- 239000000843 powder Substances 0.000 claims description 2
- 239000003795 chemical substances by application Substances 0.000 claims 1
- 150000001875 compounds Chemical class 0.000 description 4
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 229910052787 antimony Inorganic materials 0.000 description 3
- WATWJIUSRGPENY-UHFFFAOYSA-N antimony atom Chemical compound [Sb] WATWJIUSRGPENY-UHFFFAOYSA-N 0.000 description 3
- 235000002639 sodium chloride Nutrition 0.000 description 3
- CJAZCKUGLFWINJ-UHFFFAOYSA-N 3,4-dihydroxybenzene-1,2-disulfonic acid Chemical compound OC1=CC=C(S(O)(=O)=O)C(S(O)(=O)=O)=C1O CJAZCKUGLFWINJ-UHFFFAOYSA-N 0.000 description 2
- WQGWDDDVZFFDIG-UHFFFAOYSA-N pyrogallol Chemical compound OC1=CC=CC(O)=C1O WQGWDDDVZFFDIG-UHFFFAOYSA-N 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical compound OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 230000009931 harmful effect Effects 0.000 description 1
- 230000035876 healing Effects 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 229940079877 pyrogallol Drugs 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F13/00—Compounds containing elements of Groups 7 or 17 of the Periodic Table
- C07F13/005—Compounds without a metal-carbon linkage
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Description
Verfahren zur Herstellung einer löslichen lt'Ianganverbindung. Im Hauptpatent ist ein Verfahren be schrieben, nach dem man eine Komplexver bindung von Antimon mit Pyrogalloldisulfo- säure erhält. Verbindungen dieser Art un terscheiden sich von gewöhnlichen Salzen des Antirrions dadurch, dass sie eine Reihe von Reaktionen dieser Salze nicht haben.
Sie enthalten nämlich das Antimon in festerer sogenannter Komplexverbindung. Diese Stoffe sind als Heilmittel verwendbar, da in ihnen infolge der festeren Bindung des Antimons die schädliche Wirkung gegenüber der Heilwirkung zurückgedrängt ist.
Es wurde gefunden, dass die gleichen Ver hältnisse obwalten, wenn man brenzkatechin- disulfosaures Natrium mit Mangancarbonat umsetzt.
Die Ausführung .des Verfahrens erfolgt am besten in der Weise"dass man brenzkate- chindisulfosaures Natrium mit der erforder lichen Menge der Manganverbindung in wäs seriger Lösung, gegebenenfalls unter Erwär men umsetzt.
Beispiel: 54 gr benzkatechindisulfosaures Natrium werden mit 150 cm' Wasser und 11 gr Man gancarbonat einige Zeit in Kohlensäureat- mosphäre .am Rückflusskühler gekocht, nach dem Erkalten wird filtiert. Aus dem Filtrat wird durch Zusatz von Methylalkohol das gebildete Komplexsalz ausgefällt. Nach .dem Abscheiden erhält man ein graues Pulver, das sich mit gelbgrüner Farbe in Wasser löst. Das Produkt dient als Mittel gegen Infektionskrankheiten.
Process for the preparation of a soluble lt'langanese compound. The main patent describes a process according to which a complex compound of antimony with pyrogallol disulphonic acid is obtained. Compounds of this kind differ from common salts of antirion in that they do not have a number of reactions of these salts.
They contain the antimony in a more solid so-called complex compound. These substances can be used as remedies, because in them, due to the stronger binding of the antimony, the harmful effects are suppressed compared to the healing effects.
It has been found that the same conditions prevail if sodium catechol disulphonate is reacted with manganese carbonate.
The process is best carried out in such a way that sodium pyrocatechol disulphonate is reacted with the required amount of the manganese compound in an aqueous solution, optionally with heating.
Example: 54 g of catechol disulphonic acid are boiled with 150 cm of water and 11 g of manganese carbonate in a carbonic acid atmosphere on a reflux condenser, after which it is filtered. The complex salt formed is precipitated from the filtrate by adding methyl alcohol. After the deposition, a gray powder is obtained, which dissolves in water with a yellow-green color. The product is used as a remedy for infectious diseases.
Claims (1)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH123233T | 1926-01-29 | ||
| CH125392T | 1926-01-29 | ||
| CH124948T | 1926-01-29 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH124948A true CH124948A (en) | 1928-03-16 |
Family
ID=27176802
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH124948D CH124948A (en) | 1926-01-29 | 1926-01-29 | Process for producing a soluble manganese compound. |
Country Status (1)
| Country | Link |
|---|---|
| CH (1) | CH124948A (en) |
-
1926
- 1926-01-29 CH CH124948D patent/CH124948A/en unknown
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CH124948A (en) | Process for producing a soluble manganese compound. | |
| CH125391A (en) | Process for the preparation of a soluble vanadyl compound. | |
| AT106981B (en) | Process for the production of acid-free, pure, resinous condensation products from phenols and aldehydes. | |
| CH125381A (en) | Process for the preparation of a soluble vanadyl compound. | |
| CH125377A (en) | Process for producing a soluble arsenic compound. | |
| CH155688A (en) | Process for the preparation of a water-soluble antimony salt. | |
| CH125394A (en) | Process for the preparation of a soluble vanadium compound. | |
| AT126152B (en) | Process for the production of physiologically active copper-arsenic compounds. | |
| CH124949A (en) | Process for the production of a soluble cadmium compound. | |
| CH125387A (en) | Process for producing a soluble arsenic compound. | |
| CH125379A (en) | Process for the preparation of a soluble tin compound. | |
| CH125390A (en) | Process for the production of a soluble chromium compound. | |
| CH125386A (en) | Process for the preparation of a soluble vanadium compound. | |
| CH125389A (en) | Process for the preparation of a soluble tin compound. | |
| CH132212A (en) | Process for producing a solid diazoazo compound. | |
| CH125378A (en) | Process for the production of a soluble cadmium compound. | |
| CH125382A (en) | Process for producing a soluble copper compound. | |
| DE411051C (en) | Process for the preparation of derivatives of 2-phenylquinoline-4-carboxylic acid | |
| CH132204A (en) | Process for producing a solid diazoazo compound. | |
| CH124947A (en) | Process for producing a soluble copper compound. | |
| CH124943A (en) | Process for the production of a soluble cadmium compound. | |
| CH132205A (en) | Process for producing a solid diazoazo compound. | |
| CH124939A (en) | Process for producing a soluble copper compound. | |
| CH212788A (en) | Process for the preparation of an aminoarylsulfonic acid derivative. | |
| CH125393A (en) | Process for the preparation of a soluble tin compound. |