CH190717A - Process for the preparation of a new auxiliary substance. - Google Patents
Process for the preparation of a new auxiliary substance.Info
- Publication number
- CH190717A CH190717A CH190717DA CH190717A CH 190717 A CH190717 A CH 190717A CH 190717D A CH190717D A CH 190717DA CH 190717 A CH190717 A CH 190717A
- Authority
- CH
- Switzerland
- Prior art keywords
- auxiliary substance
- preparation
- new auxiliary
- new
- dissolves
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D235/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
- C07D235/02—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
- C07D235/04—Benzimidazoles; Hydrogenated benzimidazoles
- C07D235/06—Benzimidazoles; Hydrogenated benzimidazoles with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached in position 2
- C07D235/08—Radicals containing only hydrogen and carbon atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Cosmetics (AREA)
Description
Verfahren zur Darstellung eines neuen Hilfsstoffes. Es wurde gefunden, dass man einen neuen Hilfsstoff erhält, wenn man das N- 111.'ethyl-,u-n-undecylbenzimidazol mit sulfie- rend wirkenden Mitteln behandelt. Das neue Produkt bildet in Form seines Alkalisalzes eine helle Masse, die sich in \Va.sser zu einer klaren, stark schäumenden Lösung, die aus gezeichnete Wasch-, Netz- und Dispergier- eigenschaften besitzt, löst.
Das ausgezeichnete Schaumvermögen der neuen Produkte macht dasselbe zum Wa schen lebender Haare besonders wertvoll. Es kann ferner zur Herstellung von Zahnpasten oder von Schaumlöschmitteln verwendet werden. ' <I>Beispiel:</I> 67,2 Teile eines Gemisches, bestehend hauptsächlich aus ,u-n-Undecylben.zimidazot, wie es .durch Erhitzen von technischer Iiokos- fettsäure mit o-Phenylendiamin erhalten wird, werden geschmolzen und auf 125 erhitzt.
In die Schmelze lässt man sodann 25,2 Zeile Dimethylsulfat allmählich zu- fliessen und erhitzt :das Gemisch, bis eine Probe der Reaktionsmasse sich in angesäuer tem Wasser klar auflöst. Die Reaktions masse bildet nach dem Erstarren eine spröde, leicht pulverisierbare Masse.
Man gibt zu 300 Teilen Schwefelsäure bei 20 bis 25 allmählich 100 Teile des nach dem vorigen Absatz erhaltenen N- Nethylbenzimidazolgemisches. Die Sulfonie- rung vollzieht sich schon teilweise während ges Eintragens; sie wird durch Hinzuflie- ssenlas:sen von etwa 50 Teilen 24%igem Oleum im Laufe von 2 bis 3 Stunden zu Ende geführt.
Sobald eine Probe sich in ver- ,dünnten wässerigen Alkalien klar und voll ständig löst, .giesst man das Sulfonierungs- gemisch auf Eis, filtriert und wäscht mit Wasser. Die zurückbleibende Sulfonsäure wird in Wasser verteilt und mit Natrium- hydrogy.d oder -carbona.t neutralisiert.
Process for the preparation of a new auxiliary substance. It has been found that a new auxiliary is obtained if the N-111.'ethyl-, u-n-undecylbenzimidazole is treated with agents having a sulphurizing effect. The new product forms a light-colored mass in the form of its alkali salt, which dissolves in particular to form a clear, strongly foaming solution with excellent washing, wetting and dispersing properties.
The excellent foaming power of the new products makes them particularly valuable for washing living hair. It can also be used to make toothpastes or foam extinguishers. '<I> Example: </I> 67.2 parts of a mixture consisting mainly of un-undecylbenzimidazote, as is obtained by heating technical-grade iocos fatty acid with o-phenylenediamine, are melted and heated to 125 .
25.2 lines of dimethyl sulfate are then gradually poured into the melt and heated: the mixture until a sample of the reaction mass dissolves clearly in acidified water. The reaction mass forms after solidification a brittle, easily pulverizable mass.
100 parts of the N-methylbenzimidazole mixture obtained according to the previous paragraph are gradually added to 300 parts of sulfuric acid at 20-25. The sulphonation already takes place partly during the whole entry; it is completed by allowing about 50 parts of 24% oleum to flow in over the course of 2 to 3 hours.
As soon as a sample dissolves clearly and completely in dilute, aqueous alkalis, the sulfonation mixture is poured onto ice, filtered and washed with water. The remaining sulfonic acid is distributed in water and neutralized with sodium hydrogy.d or carbona.t.
Claims (1)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH190717T | 1936-04-30 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH190717A true CH190717A (en) | 1937-05-15 |
Family
ID=4437173
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH190717D CH190717A (en) | 1936-04-30 | 1936-04-30 | Process for the preparation of a new auxiliary substance. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH190717A (en) |
-
1936
- 1936-04-30 CH CH190717D patent/CH190717A/en unknown
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