CS274873B2 - N-alkylmonoazacrown-n-oxides and method of their preparation - Google Patents
N-alkylmonoazacrown-n-oxides and method of their preparationInfo
- Publication number
- CS274873B2 CS274873B2 CS548389A CS548389A CS274873B2 CS 274873 B2 CS274873 B2 CS 274873B2 CS 548389 A CS548389 A CS 548389A CS 548389 A CS548389 A CS 548389A CS 274873 B2 CS274873 B2 CS 274873B2
- Authority
- CS
- Czechoslovakia
- Prior art keywords
- alkylmonoazacrown
- oxides
- preparation
- antimicrobial effect
- aza crown
- Prior art date
Links
- 238000002360 preparation method Methods 0.000 title abstract 2
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 abstract 2
- 230000000845 anti-microbial effect Effects 0.000 abstract 2
- -1 aza crown ethers Chemical class 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- 125000004432 carbon atom Chemical group C* 0.000 abstract 1
- 230000000536 complexating effect Effects 0.000 abstract 1
- 230000000249 desinfective effect Effects 0.000 abstract 1
- 239000003599 detergent Substances 0.000 abstract 1
- 230000000694 effects Effects 0.000 abstract 1
- 239000008235 industrial water Substances 0.000 abstract 1
- 239000003960 organic solvent Substances 0.000 abstract 1
- 230000002285 radioactive effect Effects 0.000 abstract 1
- 230000003381 solubilizing effect Effects 0.000 abstract 1
- 238000001228 spectrum Methods 0.000 abstract 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 1
Landscapes
- Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
Abstract
The solution concerns antimicrobially active amphiphilic aza crown ethers of the type of N-alkylmonoazacrown-N-oxides, where R means hydrocarbonic chain with number of carbon atoms from 8 to 16 and n means 3 or 4, and their preparation method, which consists in reaction of N-alkylated aza crown ether with hydrogen peroxide at a temperature of 20 to 60 degrees C for a period of 8 hours.The above mentioned compounds are soluble in water and in organic solvents, they have wide-spectrum antimicrobial effect and are therefore utilizable as multifunctional compounds, mainly as detergents with simultaneous disinfecting and chelating effect in places, where combination of solubilizing, deterging and complexing properties and antimicrobial effect, for example also for collecting of some (even radioactive) elements from industrial waters.<IMAGE>
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CS548389A CS274873B2 (en) | 1989-09-26 | 1989-09-26 | N-alkylmonoazacrown-n-oxides and method of their preparation |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CS548389A CS274873B2 (en) | 1989-09-26 | 1989-09-26 | N-alkylmonoazacrown-n-oxides and method of their preparation |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CS548389A2 CS548389A2 (en) | 1991-11-12 |
| CS274873B2 true CS274873B2 (en) | 1991-11-12 |
Family
ID=5399821
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CS548389A CS274873B2 (en) | 1989-09-26 | 1989-09-26 | N-alkylmonoazacrown-n-oxides and method of their preparation |
Country Status (1)
| Country | Link |
|---|---|
| CS (1) | CS274873B2 (en) |
-
1989
- 1989-09-26 CS CS548389A patent/CS274873B2/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| CS548389A2 (en) | 1991-11-12 |
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