CH379036A - Detergents and disinfectants - Google Patents
Detergents and disinfectantsInfo
- Publication number
- CH379036A CH379036A CH7329759A CH7329759A CH379036A CH 379036 A CH379036 A CH 379036A CH 7329759 A CH7329759 A CH 7329759A CH 7329759 A CH7329759 A CH 7329759A CH 379036 A CH379036 A CH 379036A
- Authority
- CH
- Switzerland
- Prior art keywords
- parts
- acid
- water
- emulsion
- disinfectant
- Prior art date
Links
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q19/00—Preparations for care of the skin
- A61Q19/10—Washing or bathing preparations
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/40—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
- A61K8/44—Aminocarboxylic acids or derivatives thereof, e.g. aminocarboxylic acids containing sulfur; Salts; Esters or N-acylated derivatives thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q17/00—Barrier preparations; Preparations brought into direct contact with the skin for affording protection against external influences, e.g. sunlight, X-rays or other harmful rays, corrosive materials, bacteria or insect stings
- A61Q17/005—Antimicrobial preparations
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/02—Anionic compounds
- C11D1/04—Carboxylic acids or salts thereof
- C11D1/10—Amino carboxylic acids; Imino carboxylic acids; Fatty acid condensates thereof
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/88—Ampholytes; Electroneutral compounds
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Engineering & Computer Science (AREA)
- Dermatology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Birds (AREA)
- Epidemiology (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Detergent Compositions (AREA)
- Medicinal Preparation (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
Description
Zusatzpatent zum Hauptpatent Nr. 370182 Wasch- und Desinfektionsmittel Im Hauptpatent ist ein Wasch- und Desinfektionsmittel beschrieben, das einen Gehalt an amphoteren, oberflächenaktiven Verbindungen der Formel in der CI2H25-NHCH2CH2CH2NH-CXH2XCOOH1 C.H2X=-CH2-, -CH2CH2
EMI0001.0006
ist oder anderen wasserlöslichen Salzen mit Säuren aufweist.
Bei der Weiterentwicklung wurde nun gefunden, dass die Verwendung des obengenannten Wasch- und Desinfektionsmittels besonders vorteilhaft ist, wenn es eine Emulsion ist, deren Dispersionsmittel aus einer wässrigen Lösung besteht, die amphotere oberflächenaktive Verbindungen der obengenannten Formel oder deren wasserlösliche Salze mit Säuren enthält, und deren disperse Phase in Wasser unlös liche Fettsäurealkylolamide enthält.
Fettsäurealkylolamide, die besonders für diese Verwendung in Betracht kommen, sind z. B. solche der höheren gesättigten Fettsäuren Palmitinsäure oder Stearinsäure mit Monoäthanolamin. Der Zusatz kann etwa 1-10% betragen.
Die Verwendung des erfindungsgemässen Wasch- und Desinfektionsmittels in Emulsionsform hat gegen über der Verwendung der einfachen wässrigen Lö sungen Vorzüge von zweierlei Art, besonders wenn sie der Händedesinfektion dient.
1. Die dickflüssige Form der Emulsion erleichtert ihre unmittelbare Verwendung zum Waschen der Hände insofern, als sie beim Aufbringen auf die Hand nicht abfliesst und sich gut auf der ganzen Handfläche verteilen lässt.
2. Der in der Emulsion enthaltene Fettstoff, der die baktericide Wirkung des Desinfektionsmittels nicht beeinträchtigt, wirkt auf der Haut als Schutzstoff und Rückfettungsmittel, so dass durch diese Anwendungsform erstmalig ein Mittel er halten wird, das Waschvermögen, Desinfektions wirkung und Hautpflege kombiniert.
<I>Beispiele</I> 1. 15 Teile N-Dodecyl-1,3-aminopropyl-f amino- buttersäure, 1,5 Teile Weinsäure und 4 Teile Stearin säurernonoäthanolamid werden in 80 Teilen Wasser bei 90 gelöst. Die zunächst klare Lösung gibt beim Kaltrühren eine dickflüssige milchweisse Emulsion, die gegebenenfalls parfümiert werden kann. Die Emulsion ist ein ausgezeichnetes Mittel zur chirur gischen Händedesinfektion.
2. 7,5 Teile N-Dodecyl-1,3-aminopropyl-ss-amino- buttersäure, 7,5 Teile Dodecyl-di(aminoäthyl)-glycin, 2 Teile Weinsäure und 5 Teile Stearinsäuremono- äthanolamid werden in 78 Teilen heissem Wasser ge löst und zur Emulsion kalt gerührt.
3. 7,5 Teile N-Dodecyl-1,3-aminopropyl-ss-amino- buttersäure, 7,5 Teile O-Dodecyl-1,3-oxypropyl-#- aminobuttersäure, 1,5 Teile Weinsäure und 3 Teile Stearinsäureäthanolamid werden in 80 Teilen heissem Wasser gelöst. Bei Kaltrühren entsteht eine dick flüssige Emulsion.
4. 20 Teile N-Dodecyl-1,3-aminopropyl-amino- essigsäure, 2 Teile Citronensäure und 8 Teile Pal- mitinsäure-monoäthanolamid werden in 70 Teilen heissem Wasser gelöst und zur Emulsion kaltgerührt.
Additional patent to the main patent No. 370182 Washing and disinfecting agents The main patent describes a washing and disinfecting agent that contains amphoteric, surface-active compounds of the formula CI2H25-NHCH2CH2CH2NH-CXH2XCOOH1 C.H2X = -CH2-, -CH2CH2
EMI0001.0006
or has other water-soluble salts with acids.
In the further development it has now been found that the use of the above-mentioned detergent and disinfectant is particularly advantageous if it is an emulsion whose dispersant consists of an aqueous solution containing amphoteric surface-active compounds of the above formula or their water-soluble salts with acids, and whose disperse phase contains fatty acid alkylolamides which are insoluble in water.
Fatty acid alkylolamides which are particularly suitable for this use are, for. B. those of the higher saturated fatty acids palmitic acid or stearic acid with monoethanolamine. The addition can be about 1-10%.
The use of the detergent and disinfectant according to the invention in emulsion form has advantages of two types over the use of simple aqueous solutions, especially when it is used for hand disinfection.
1. The viscous form of the emulsion facilitates its direct use for washing the hands insofar as it does not run off when applied to the hand and can be easily spread over the entire palm.
2. The fatty substance contained in the emulsion, which does not impair the bactericidal effect of the disinfectant, acts on the skin as a protective substance and refatting agent, so that for the first time an agent is obtained that combines washing power, disinfectant effect and skin care with this application.
<I> Examples </I> 1. 15 parts of N-dodecyl-1,3-aminopropyl-f aminobutyric acid, 1.5 parts of tartaric acid and 4 parts of stearic acid nanoethanolamide are dissolved in 80 parts of water at 90 °. The initially clear solution gives a viscous milk-white emulsion on cold stirring, which can optionally be perfumed. The emulsion is an excellent means of surgical hand disinfection.
2. 7.5 parts of N-dodecyl-1,3-aminopropyl-s-aminobutyric acid, 7.5 parts of dodecyl-di (aminoethyl) -glycine, 2 parts of tartaric acid and 5 parts of stearic acid monoethanolamide are dissolved in 78 parts of hot water ge dissolved and stirred cold to emulsion.
3. 7.5 parts of N-dodecyl-1,3-aminopropyl-s-aminobutyric acid, 7.5 parts of O-dodecyl-1,3-oxypropyl - # - aminobutyric acid, 1.5 parts of tartaric acid and 3 parts of stearic acid ethanolamide dissolved in 80 parts of hot water. Cold stirring creates a thick, liquid emulsion.
4. 20 parts of N-dodecyl-1,3-aminopropylaminoacetic acid, 2 parts of citric acid and 8 parts of palmitic acid monoethanolamide are dissolved in 70 parts of hot water and stirred until cold to emulsion.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DEG22432A DE1041627B (en) | 1957-06-29 | 1957-06-29 | Detergents and disinfectants |
DEG25989A DE1066693B (en) | 1957-06-29 | 1958-12-19 | Detergents and disinfectants |
Publications (1)
Publication Number | Publication Date |
---|---|
CH379036A true CH379036A (en) | 1964-06-30 |
Family
ID=25978097
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH6010958A CH370182A (en) | 1957-06-29 | 1958-05-30 | Detergents and disinfectants |
CH7329759A CH379036A (en) | 1957-06-29 | 1959-05-15 | Detergents and disinfectants |
Family Applications Before (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH6010958A CH370182A (en) | 1957-06-29 | 1958-05-30 | Detergents and disinfectants |
Country Status (6)
Country | Link |
---|---|
BE (2) | BE568919A (en) |
CH (2) | CH370182A (en) |
DE (2) | DE1041627B (en) |
FR (1) | FR1198334A (en) |
GB (2) | GB836956A (en) |
NL (1) | NL239449A (en) |
Families Citing this family (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1130957B (en) * | 1961-02-11 | 1962-06-07 | Goldschmidt Ag Th | Germicides cold washing process |
DE1184770C2 (en) * | 1961-06-01 | 1965-09-02 | Hoffmann La Roche | Process for the production of antibacterially active peptides |
DE1617097A1 (en) * | 1966-03-26 | 1971-02-25 | Goldschmidt Ag Th | Pieces of hand disinfectant |
US4224319A (en) | 1979-07-31 | 1980-09-23 | Ernest Marcadet | Antiseptic composition for topical application to the skin |
DE3528209C2 (en) * | 1984-08-07 | 1993-10-28 | Fresenius Ag | disinfectant |
CN114788521B (en) * | 2022-03-23 | 2024-01-26 | 广州先进技术研究所 | Composite synergistic multifunctional disinfectant and preparation method thereof |
-
0
- BE BE579035D patent/BE579035A/xx unknown
- NL NL239449D patent/NL239449A/xx unknown
- BE BE568919D patent/BE568919A/xx unknown
-
1957
- 1957-06-29 DE DEG22432A patent/DE1041627B/en active Pending
-
1958
- 1958-02-19 GB GB543358A patent/GB836956A/en not_active Expired
- 1958-05-30 CH CH6010958A patent/CH370182A/en unknown
- 1958-06-27 FR FR1198334D patent/FR1198334A/en not_active Expired
- 1958-12-19 DE DEG25989A patent/DE1066693B/en active Pending
-
1959
- 1959-05-15 CH CH7329759A patent/CH379036A/en unknown
- 1959-06-05 GB GB1938459A patent/GB848654A/en not_active Expired
Also Published As
Publication number | Publication date |
---|---|
CH370182A (en) | 1963-06-30 |
DE1066693B (en) | 1959-10-08 |
GB848654A (en) | 1960-09-21 |
DE1041627B (en) | 1958-10-23 |
BE568919A (en) | |
FR1198334A (en) | 1959-12-07 |
GB836956A (en) | 1960-06-09 |
BE579035A (en) | |
NL239449A (en) |
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