WO2000061709A2 - Handwashing pastes - Google Patents
Handwashing pastes Download PDFInfo
- Publication number
- WO2000061709A2 WO2000061709A2 PCT/EP2000/002847 EP0002847W WO0061709A2 WO 2000061709 A2 WO2000061709 A2 WO 2000061709A2 EP 0002847 W EP0002847 W EP 0002847W WO 0061709 A2 WO0061709 A2 WO 0061709A2
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- alcohol
- hand washing
- acid
- amounts
- pastes according
- 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.)
- Ceased
Links
Classifications
-
- 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
- C11D17/00—Detergent materials or soaps characterised by their shape or physical properties
- C11D17/0008—Detergent materials or soaps characterised by their shape or physical properties aqueous liquid non soap compositions
- C11D17/0013—Liquid compositions with insoluble particles in suspension
-
- 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
- C11D1/66—Non-ionic compounds
- C11D1/667—Neutral esters, e.g. sorbitan esters
-
- 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
- C11D1/66—Non-ionic compounds
- C11D1/83—Mixtures of non-ionic with anionic compounds
-
- 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
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/02—Inorganic compounds ; Elemental compounds
- C11D3/12—Water-insoluble compounds
- C11D3/14—Fillers; Abrasives ; Abrasive compositions; Suspending or absorbing agents not provided for in one single group of C11D3/12; Specific features concerning abrasives, e.g. granulometry or mixtures
-
- 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
- C11D1/12—Sulfonic acids or sulfuric acid esters; Salts thereof
- C11D1/14—Sulfonic acids or sulfuric acid esters; Salts thereof derived from aliphatic hydrocarbons or mono-alcohols
- C11D1/146—Sulfuric acid esters
-
- 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
- C11D1/12—Sulfonic acids or sulfuric acid esters; Salts thereof
- C11D1/29—Sulfates of polyoxyalkylene ethers
Definitions
- the present invention relates to hand wash pastes containing anionic surfactants, friction bodies and partial glycerides, in particular oleic acid monoglycerides, and to the use of such partial glycerides to improve the feeling of the skin and the development of foam in hand wash pastes.
- Handwashing pastes are used in the commercial sector to remove strongly adhering soiling on the skin, which usually also have only a low solubility in water, for example oils, greases, paint residues and the like. Handwash pastes of this type contain, in addition to tensides, rubbing agents to remove the stubborn dirt, which ensure additional mechanical cleaning of the skin.
- European patent application EP 0 881 281 describes hand washing pastes which contain a synthetic anionic surfactant, at least one nonionic surfactant mixture, at least one long-chain carboxylic acid and a water-soluble abrasive in solid, finely divided form.
- the object of the present invention was therefore to provide mild hand wash pastes which have an improved compatibility with the skin, so that the skin is perceived as smoother.
- the mild hand washing pastes should ensure an improved foam texture, ie a creamier and more fine-pored foam.
- the mild handwashing pastes should have a high cleaning performance, even for the most stubborn dirt, despite their improved skin tolerance.
- the task could surprisingly be achieved if the hand wash pastes additionally contain partial glycerides.
- One object of the present invention therefore relates to hand-washing pastes with improved skin feel and foaming power, comprising a) anionic surfactants b) friction bodies c) partial glycerides.
- Partial glycerides ie monoglycerides, diglycerides and their technical mixtures, can still contain small amounts of triglycerides due to the production process.
- the partial glycerides preferably follow the formula (I)
- R 2 and R 3 independently of one another for R'CO or OH and the sum (m + n + p ) stands for 0 or numbers from 1 to 100, preferably 5 to 25, with the proviso that at least one of the two radicals R 2 and R 3 stands for OH.
- Typical examples are mono- and / or diglycerides based on caproic acid, caprylic acid, 2-ethylhexanoic acid, capric acid, lauric acid, isotridecanoic acid, myristic acid, palmitic acid, palmoleic acid, stearic acid, isostearic acid, oleic acid, elaidic acid, petroselinic acid, linoleic acid, linoleic acid, Linolenic acid, elaeostearic acid, arachic acid, gadoleic acid, behenic acid and erucic acid and their technical mixtures.
- partial ric acid glycerides partial palmitic acid glycerides, partial stearic acid glycerides, partial isostearic acid glycerides, partial oleic acid glycerides, partial behenic glycerides and / or partial erucic acid glycerides, which have a monoglyceride content in the range from 50 to 95, preferably 60 to 90% by weight.
- Partial glycerides of the formula (I) in which R'CO is an unsaturated acyl radical with 18 carbon atoms, the sum (m + n + p) for 0, R 2 for OH or an unsaturated acyl radical with 18 carbon atoms and R 3 are very particularly preferred stands for OH, ie technical oleic acid partial glycerides, in particular those which have a monoglyceride content in the range from 50 to 95, preferably 60 to 90,% by weight.
- the partial glycerides are preferably present in amounts of 1 to 10% by weight, preferably in amounts of 2 to 7% by weight, based on hand-washing paste.
- friction bodies which are often also referred to as abrasives.
- Suitable friction bodies include, for example, wood flour, grated pumice stone, nutshell and / or plant fiber ground material, chalk, quartz sand and ground plastics, for example polyethylene flour, alone or as a mixture.
- Typical examples are ground wood fiber (Lignocell ® BK 40/90, mesh size 150 ⁇ m: max.
- UNG 300 Rettenmeier & Co., Ellwangen / FRG; particle range 170 to 230 ⁇ m
- chalk cristobalite flour -M -006®; Quarzwerke Frechen
- quartz sand F34® Frechen quartz movement and / or Lupolen 1800 S P15® as polyethylene flour.
- Wood flour, quartz sand, chalk and / or polyethylene flour are preferably contained as the friction body.
- the friction bodies are preferably used in amounts of 1 to 50, preferably in amounts of 15 to 45% by weight, based on the hand washing paste.
- these can be partially substituted as co-friction bodies by adding inorganic and / or organic salts. Salts such as alkali and / or alkaline earth carbonates, sulfates, chlorides, hydrogen carbonates, citrates and silicates are suitable for this purpose.
- Other mandatory components of the hand wash pastes according to the invention are anionic surfactants.
- anionic surfactants are soaps, alkylbenzenesulfonates alkanesulfonates, Al, sulfonates olefin sulfonates, alkyl ether sulfonates, glycerol ether, -Methylestersul-, sulfofatty acids, alkyl sulfates, fatty alcohol ether sulfates, Glycerol ether, fatty reethersulfate, Hydroxymischethersulfate, monoglyceride (ether) sulfates, fatty acid amide (ether ) sulfates, mono- and dialkylsulfosuccinates, mono- and dialkylsulfosuccinamates, sulfotriglycerides, amide soaps, ether carboxylic acids and their salts, fatty acid isethionates, fatty acid sarcosinates, fatty acid taurides, N-
- anionic surfactants contain polyglycol ether chains, they can have a conventional, but preferably a narrow, homolog distribution.
- the anionic surfactants are preferably present in amounts of 1 to 30% by weight, preferably 5 to 25% by weight, based on handwashing paste.
- fatty alcohol sulfates and / or fatty alcohol ether sulfates are preferably present as anionic surfactants.
- Fatty alcohol sulfates are to be understood as meaning the sulfation products of primary alcohols which follow the formula (II)
- R 4 represents a linear or branched, aliphatic alkyl and / or alkenyl radical having 6 to 22, preferably 12 to 18 carbon atoms and X represents an alkyl and / or alkaline earth metal, ammonium, alkylammonium, alkanolammonium or glucammonium.
- Typical examples of fatty alcohol sulfates which can be used in the context of the invention are the sulfation products of capron alcohol, caprylic alcohol, capric alcohol, 2-ethylhexyl alcohol, lauryl alcohol, myristyl alcohol, cetyl alcohol, palmoleyl alcohol, stearyl alcohol, isostearyl alcohol, oleyl alcohol, aridyl alcohol, arachidyl alcohol, elaidol alcohol, elaid alcohol alcohol, gadoleyl alcohol, behenyl alcohol and erucyl alcohol and their technical mixtures, which are characterized by high-pressure hydrogenation of technical methyl ester fractions or aldehydes the Roelen 'see oxosynthesis can be obtained.
- the sulfation products can preferably be used in the form of their alkali metal salts, and in particular their sodium salts.
- Alkyl sulfates based on C ] 2 are particularly preferred.
- 18 fatty alcohol cuts in the form of their sodium salts.
- the fatty alcohol sulfates are preferably present in amounts of 5 to 25% by weight, preferably 10 to 20% by weight, calculated as the active substance content and based on handwashing paste.
- fatty alcohol ether sulfates can be present as the sole anionic surfactant, preferably they are contained in a mixture with the fatty alcohol sulfates already described.
- the fatty alcohol ether sulfates are preferably present in amounts of 0 to 5% by weight, preferably in amounts of 0 to 3% by weight, calculated as the active substance content and based on handwashing paste.
- Fatty alcohol ether sulfates (“ether sulfates”) are known anionic surfactants which are produced on an industrial scale by SO 3 or CSA sulfation of fatty alcohol polyglycol ethers and subsequent neutralization.
- ether sulfates which follow the formula (III) are suitable
- R 5 represents a linear or branched alkyl and / or alkenyl radical with 6 to 22 carbon atoms, 1 for numbers from 1 to 10 and X for an alkali and / or alkaline earth metal, ammonium, alkylammonium, alkanolammonium or glucammonium.
- Typical examples are the sulfates of addition products with an average of 1 to 10 and in particular 2 to 5 mol ethylene oxide onto capron alcohol, caprylic alcohol, 2-ethylhexyl alcohol, capric alcohol, lauryl alcohol, isotridecyl alcohol, myristyl alcohol, cetyl alcohol, palmoleyl alcohol, stearyl alcohol, isostyl alcohol, isostearyl alcohol Elaidyl alcohol, petroseline alcohol, arachyl alcohol, gadoleyl alcohol, behenyl alcohol and erucyl alcohol and their technical mixtures, in the form of their sodium and / or magnesium salts.
- the ether sulfates can have both a conventional and a narrow homolog distribution.
- ether sulfates based on adducts is particularly preferred of on average 2 to 3 moles of ethylene oxide with technical C I2 / I4 - or C 12 /] 8 -Kokosfettalkoholfrak- functions in the form of their sodium and / or magnesium salts.
- the handwashing pastes according to the invention can optionally contain further nonionic surfactants, the particle glycerides not being added to the other nonionic surfactants.
- Typical examples of further nonionic surfactants are fatty alcohol polyglycol ethers, alkylphenol polyglycol ethers, fatty acid polyglycol esters, fatty acid amide polyglycol ethers, fatty amine polyglycol ethers, alkoxylated triglycerides, mixed ethers or mixed formals, optionally partially oxidized alk (en) yl oligoglycosides, in particular -glycosyl glucosilicate acid derivatives (GLC), glucorosulfonic acid derivatives (F) vegetable products based on wheat), polyol fatty acid esters, sugar esters, sorbitan esters, polysorbates and amine oxides.
- further nonionic surfactants are fatty alcohol polyglycol ethers, alkylphenol poly
- nonionic surfactants contain polyglycol ether chains, they can have a conventional, but preferably a narrow, homolog distribution. Fatty alcohol polyglycol ethers and / or alk (en) yl oligoglycosides are preferably contained as further nonionic surfactants.
- Fatty alcohol polyglycol ethers are known nonionic surfactants which are produced on an industrial scale by alkoxylation of fatty alcohols in the presence of acidic, but preferably alkaline, catalysts.
- the polyglycol ethers can be ethylene oxide (EO), propylene oxide (PO) or EO / PO adducts - the latter with random or block distribution.
- fatty alcohol polyglycol ethers of the formula (IV) are suitable
- R 6 represents a linear or branched alkyl and / or alkenyl radical having 6 to 22 carbon atoms and z represents numbers from 1 to 10.
- Typical examples are addition products of an average of 1 to 10 and in particular 3 to 7 mol of ethylene oxide with capron alcohol, caprylic alcohol, 2-ethylhexyl alcohol, capric alcohol, lauryl alcohol, isotridecyl alcohol, myristyl alcohol, cetyl alcohol, palmoleyl alcohol, stearyl alcohol, isostearyl alcohol, elaalyl alcohol, oleyl alcohol, oleyl alcohol - alcohol, gadoleyl alcohol, behenyl alcohol and erucyl alcohol and their technical mix in the form of their sodium and / or magnesium salts.
- the polyglycol ethers can have both a conventional and a narrow homolog distribution.
- the use of adducts of an average of 3 to 7 moles of ethylene oxide with technical coconut oil alcohol or oleyl alcohol fractions is particularly preferred.
- Alkyl and alkenyl oligoglycosides are known substances which can be obtained by the relevant processes in preparative organic chemistry and follow the formula (V),
- R 7 represents an alkyl and or alkenyl radical having 4 to 22 carbon atoms
- G represents a sugar radical having 5 or 6 carbon atoms
- q represents a number from 1 to 10.
- the alkyl and / or alkenyl oligoglycosides can be derived from aldoses or ketoses with 5 or 6 carbon atoms, preferably glucose.
- the preferred alkyl and / or alkenyl oligoglycosides are thus alkyl and / or alkenyl oligoglucosides.
- the alkyl or alkenyl radical R 7 can be derived from primary alcohols having 8 to 16, preferably 8 to 14, carbon atoms. Typical examples are caprylic alcohol, capric alcohol, undecyl alcohol, lauryl alcohol, myristyl alcohol, cetyl alcohol, palmoleyl alcohol and their technical mixtures, such as those used in the hydrogenation of technical fatty acid methyl esters or in the course of the hydrogenation of aldehydes from Roelen's oxosynthesis.
- the nonionic surfactants are preferably present in amounts of 0 to 20% by weight, preferably in amounts of 0.1 to 10% by weight, calculated as the active substance content and based on hand washing paste.
- the hand washing pastes according to the invention can optionally contain zwitterionic or ampholytic surfactants.
- Typical examples of amphoteric or zwitterionic surfactants are alkyl betaines, alkyl amido betaines, aminopropionates, aminoglycinates, imidazolinium betaines and sulfobetaines.
- the surfactants mentioned are exclusively known compounds.
- Alkyl betaines and / or alkyl amido betaines are preferably contained as zwitterionic or ampholytic surfactants.
- Betaines are known surfactants which are predominantly produced by carboxyalkylation, preferably carboxymethylation, of aminic compounds.
- the starting materials are preferably condensed with halocarboxylic acids or their salts, in particular with sodium chloroacetate, one mol of salt being formed per mole of betaine.
- unsaturated carboxylic acids such as acrylic acid is also possible.
- betaines and "real" amphoteric surfactants reference is made to the contribution by U.Ploog in Seifen- ⁇ le-Fette-Wwachs, 198, 373 (1982). Further overviews on this topic can be found for example by A. O'Lennick et al.
- betaines are the carboxyalkylation products of secondary and in particular tertiary amines which follow the formula (VI)
- Typical examples are the carboxymethylation products of hexylmethylamine methylamine, Hexyldi-, octyldimethylamine, decyldimethylamine, dodecylmethylamine, Dodecyldime- methylamine, Dodecylethylmethylarnin, C 12/14 -Kokosalkyldimethylamin, myristyldimethylamine, cetyldimethylamine, stearyldimethylamine, stearyl, oleyl, C 16/18 tallow alkyl dimethyl amine, and their technical Mixtures.
- R u CO is an aliphatic acyl radical having 6 to 22 carbon atoms and 0 or 1 to 3 double bonds
- a is a number from 1 to 3 and R 9 , R 10 , b and Y have the meanings given above.
- Typical examples are reaction products of fatty acids with 6 to 22 carbon atoms, namely caproic acid, caprylic acid, capric acid, lauric acid, myristic acid, palmitic acid, palmoleic acid, stearic acid, isostearic acid, oleic acid, elaidic acid, petroselinic acid, linoleic acid, linolenic acid, arenachic acid, gadeleostearic acid, gaoleostolic acid , Behenic acid and erucic acid and their technical mixtures, with N, N-dimethylaminoethylamine, N, N-dimethylaminopropylamine, N, N-diethylaminoethylamine and N, N-diethylaminopropylamine, which are condensed with sodium chloroacetate.
- a condensation product of C g / ls coconut fatty acid N, N-dimethylaminopropylamide with sodium chloroacetate is preferred.
- the zwitterionic or ampholytic surfactants are preferably present in amounts from 0 to 30, preferably from 0.1 to 20, calculated as the active substance content and based on hand washing paste.
- the hand wash pastes according to the invention can furthermore contain typical additives in customary amounts.
- typical additives are fatty acids, foam boosters, dyes, fragrances, pH regulators, emulsifiers, preservatives, sequestering agents and possibly foam regulators.
- Suitable fatty acids are carboxylic acids with 10 to 22 hydrocarbon atoms, which are preferably saturated.
- a typical example is hydrogenated trans fatty acid.
- Such fatty acids can be present in amounts of 0 to 10% by weight, preferably in amounts of 0 to 2% by weight.
- Typical examples of suitable O / W or W / O emulsifiers are hardened and ethoxylated castor oil, polyglycerol fatty acid esters or polyglycerol polyricinoleates. Such emulsifiers can be present in amounts of 0 to 5% by weight, preferably 0 to 2% by weight, based on handwashing paste.
- Suitable foam boosters are e.g. Fatty acid alkanol amides, especially coconut fatty acid diethanolamide. The foam boosters can be used in amounts of 0 to 3, preferably in amounts of 0.1 to 1.5% by weight, based on hand washing paste
- the pH value of the handwashing pastes can be adjusted using pH regulators. If particularly mild agents are desired, pH values between 4.0 and 9, preferably between 5.5 and 8 are recommended. To remove stubborn dirt, it is recommended to adjust the agents more alkaline to pH values from 8 to 14, preferably from 9 , 5 to 11.
- the known water-soluble hydroxides, in particular sodium hydroxide, are suitable for adjustment. If desired, the pH can also be adjusted using a buffer system. Suitable preservatives are, for example, aldehydes such as benzaldehyde or benzyl alcohol, which are preferably present in amounts of up to 1% by weight.
- the remaining 100% by weight of the rest of the handwashing pastes is water, possibly in a mixture with other other water-soluble solvents, preferably water alone.
- the water content of the pastes is preferably in the range from 20 to 60, preferably 25 to 55% by weight, based on hand-washing paste.
- the handwashing pastes according to the invention can be produced in the usual way by mixing the components, the surfactant components usually being introduced as an aqueous paste.
- the calculated amount of water is introduced and the anionic surfactant is dissolved therein, preferably at slightly elevated temperatures of about 60 to 100 ° C.
- the partial glycerides as well as any other surfactants and usual constituents are stirred in.
- the friction bodies are incorporated and finally the desired pH value is set by adding the pH value regulators.
- the handwashing pastes according to the invention produce a pleasant feeling on the skin when washing, which is perceived as smoother and less rubbing and scratching.
- the foam generated during use is felt to be creamy and fine-pored.
- Another object of the present invention therefore relates to the use of partial glycerides to improve the feeling on the skin and the foaming of hand wash pastes.
- the handwashing pastes were prepared by stirring the compounds listed in Table 1 in the proportions shown there:
- Lamesoft PO 65® Commercial product from Henkel KGaA; Active substance content approx. 65% by weight
- Glucopon 650 EC® commercial product from Henkel KGaA; Active substance content approx. 51% by weight
- a commercial product 1 (with wood flour) was used as a comparison, which according to the company stated aqua, lignum, sodium tallow sulfate, sodium lauryl sulfate, sodium C14-17 alkyl lake sulfonate; Cocoamidopropyl betaine, cellulose gum; Soyamide DEA; Sodium citrate; Perfume; Citric acid; Benzyl alcohol; Methylchloroisothiazolinone (INCI nomenclature) contained.
- Commercial product 2 (with quartz sand) contained, according to its own information, silica, aqua; Paraffinum liquidum; Kaolin; Sodium carbonate; Oleic acid; Palmitic acid; Linoleic acid; Disodium pyrophosphate; Cocoamide DEA; Potassium hydroxide; Triethanolamines; Cellulose gum; Glycerin; Cocoamidopropyl betaines; Stearic acid; 1-phenylethanol; Benzaldehydes (according to INCI).
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Cosmetics (AREA)
- Detergent Compositions (AREA)
Abstract
Description
HandwaschpastenHand washing pastes
Die vorliegende Erfindung betrifft Handwaschpasten enthaltend anionische Tenside, Reibkörper und Partialglyceride, insbesondere Olsäuremonoglyceride, sowie die Verwendung derartiger Partialglyceride zur Verbesserung des Hautgefühls und der Schaumentwicklung von Handwaschpasten.The present invention relates to hand wash pastes containing anionic surfactants, friction bodies and partial glycerides, in particular oleic acid monoglycerides, and to the use of such partial glycerides to improve the feeling of the skin and the development of foam in hand wash pastes.
Handwaschpasten werden im gewerblichen Bereich zur Entfernung von stark haftenden An- schmutzungen auf der Haut, die meist zudem nur eine geringe Löslichkeit in Wasser aufweisen, beispielsweise Öle, Fette, Lackreste und dergleichen, eingesetzt. Derartige Handwaschpasten enthalten zur Entfernung der hartnäckigen Verschmutzungen neben Tensiden auch Reibkörper, die eine zusätzliche mechanische Reinigung der Haut gewährleisten.Handwashing pastes are used in the commercial sector to remove strongly adhering soiling on the skin, which usually also have only a low solubility in water, for example oils, greases, paint residues and the like. Handwash pastes of this type contain, in addition to tensides, rubbing agents to remove the stubborn dirt, which ensure additional mechanical cleaning of the skin.
So werden in der europäischen Patentanmeldung EP 0 881 281 Handwaschpasten beschrieben, die ein synthetisches Aniontensid, mindestens ein nichtionisches Tensidgemisch, mindestens eine langkettige Carbonsäure und einen wasserlöslichen Abrasivstoff in fester, feinverteilter Form enthalten.For example, European patent application EP 0 881 281 describes hand washing pastes which contain a synthetic anionic surfactant, at least one nonionic surfactant mixture, at least one long-chain carboxylic acid and a water-soluble abrasive in solid, finely divided form.
Da derartige Handwaschpasten mit Reibkörpern meist mehrfach täglich in den gewerblichen Betrieben angewendet werden, bedeutet dies eine besondere Beanspruchung der Haut des Anwenders, was sich durch ein rauhes Hautgefühl bemerkbar macht. Zusätzlich wird die Schaumbeschaffenheit solcher Reibkörper enthaltenden Handwaschpasten von den Anwendern oft als grobporig kritisiert.Since such hand washing pastes with rubbing bodies are mostly used several times a day in commercial operations, this means that the skin of the user is particularly stressed, which is noticeable by a rough feeling on the skin. In addition, the foam properties of such hand washing pastes containing friction bodies are often criticized by the users as having large pores.
Die Aufgabe der vorliegenden Erfindung hat somit darin bestanden, milde Handwaschpasten zur Verfügung zu stellen, die eine verbesserte Verträglichkeit mit der Haut aufweisen, so daß die Haut als glatter empfunden wird. Gleichzeitig sollten die milden Handwaschpasten eine verbesserte Schaumbeschaffenheit, d.h. einen cremigeren und feinporigeren Schaum gewährleisten. Schließlich sollten die milden Handwaschpasten trotz der verbesserten Hautverträglichkeit eine hohe Reinigungsleistung auch für hartnäckigsten Schmutz aufweisen.The object of the present invention was therefore to provide mild hand wash pastes which have an improved compatibility with the skin, so that the skin is perceived as smoother. At the same time, the mild hand washing pastes should ensure an improved foam texture, ie a creamier and more fine-pored foam. After all, the mild handwashing pastes should have a high cleaning performance, even for the most stubborn dirt, despite their improved skin tolerance.
Die Aufgabe konnte überraschenderweise dadurch gelöst werden, wenn die Handwaschpasten zusätzlich Partialglyceride enthalten.The task could surprisingly be achieved if the hand wash pastes additionally contain partial glycerides.
Ein Gegenstand der vorliegenden Erfindung betrifft daher Handwaschpasten mit verbessertem Hautgefühl und Schaumvermögen enthaltend a) anionische Tenside b) Reibkörper c) Partialglyceride.One object of the present invention therefore relates to hand-washing pastes with improved skin feel and foaming power, comprising a) anionic surfactants b) friction bodies c) partial glycerides.
Partialglyceride, also Monoglyceride, Diglyceride und deren technische Gemische können herstellungsbedingt noch geringe Mengen Triglyceride enthalten. Die Partialglyceride folgen vorzugsweise der Formel (I),Partial glycerides, ie monoglycerides, diglycerides and their technical mixtures, can still contain small amounts of triglycerides due to the production process. The partial glycerides preferably follow the formula (I)
CH2O(CH2CH2O)mCOR1 (I)CH 2 O (CH 2 CH 2 O) m COR 1 (I)
II.
CHO(CH2CH2O)nR2 CHO (CH 2 CH 2 O) n R 2
I CH2O(CH2CH2O)pR3 I CH 2 O (CH 2 CH 2 O) p R 3
in der R'CO für einen linearen oder verzweigten, gesättigten und/oder ungesättigten Acylrest mit 6 bis 22, vorzugsweise 12 bis 18 Kohlenstoffatomen, R2 und R3 unabhängig voneinander für R'CO oder OH und die Summe (m+n+p) für 0 oder Zahlen von 1 bis 100, vorzugsweise 5 bis 25 steht, mit der Maßgabe, daß mindestens einer der beiden Reste R2 und R3 für OH steht.in the R'CO for a linear or branched, saturated and / or unsaturated acyl radical having 6 to 22, preferably 12 to 18 carbon atoms, R 2 and R 3 independently of one another for R'CO or OH and the sum (m + n + p ) stands for 0 or numbers from 1 to 100, preferably 5 to 25, with the proviso that at least one of the two radicals R 2 and R 3 stands for OH.
Typische Beispiele sind Mono- und/oder Diglyceride auf Basis von Capronsäure, Capryl- säure, 2-Ethylhexansäure, Caprinsäure, Laurinsäure, Isotridecansäure, Myristinsäure, Pal- mitinsäure, Palmoleinsäure, Stearinsäure, Isostearinsäure, Ölsäure, Elaidinsäure, Petroselin- säure, Linolsäure, Linolensäure, Elaeostearinsäure, Arachinsäure, Gadoleinsäure, Behensäure und Erucasäure sowie deren technische Mischungen. Vorzugsweise werden technische Lau- rinsäurepartialglyceride, Palmitinsäurepartialglyceride, Stearinsäurepartialglyceride, Isostea- rinsäurepartialglyceride, Ölsäurepartialglyceride, Behensäurepartialglyceride und/oder Erucasäurepartialglyceride eingesetzt, welche einen Monoglyceridanteil im Bereich von 50 bis 95, vorzugsweise 60 bis 90 Gew.-% aufweisen.Typical examples are mono- and / or diglycerides based on caproic acid, caprylic acid, 2-ethylhexanoic acid, capric acid, lauric acid, isotridecanoic acid, myristic acid, palmitic acid, palmoleic acid, stearic acid, isostearic acid, oleic acid, elaidic acid, petroselinic acid, linoleic acid, linoleic acid, Linolenic acid, elaeostearic acid, arachic acid, gadoleic acid, behenic acid and erucic acid and their technical mixtures. Technical la partial ric acid glycerides, partial palmitic acid glycerides, partial stearic acid glycerides, partial isostearic acid glycerides, partial oleic acid glycerides, partial behenic glycerides and / or partial erucic acid glycerides, which have a monoglyceride content in the range from 50 to 95, preferably 60 to 90% by weight.
Ganz besonders bevorzugt werden Partialglyceride der Formel (I), in der R'CO für einen ungesättigten Acylrest mit 18 Kohlenstoffatomen, die Summe (m+n+p) für 0, R2 für OH oder einen ungesättigten Acylrest mit 18 Kohlenstoffatomen und R3 für OH steht, d.h. technische Ölsäurepartialglyceride, insbesondere solche, die einen Monoglyceridanteil im Bereich von 50 bis 95, vorzugsweise 60 bis 90 Gew.-% aufweisen.Partial glycerides of the formula (I) in which R'CO is an unsaturated acyl radical with 18 carbon atoms, the sum (m + n + p) for 0, R 2 for OH or an unsaturated acyl radical with 18 carbon atoms and R 3 are very particularly preferred stands for OH, ie technical oleic acid partial glycerides, in particular those which have a monoglyceride content in the range from 50 to 95, preferably 60 to 90,% by weight.
Die Partialglyceride sind vorzugsweise in Mengen von 1 bis 10 Gew.-%, bevorzugt in Mengen von 2 bis 7 Gew.-% - bezogen auf Handwaschpaste - enthalten.The partial glycerides are preferably present in amounts of 1 to 10% by weight, preferably in amounts of 2 to 7% by weight, based on hand-washing paste.
Ein weiterer zwingender Bestandteil der Handwaschpasten sind Reibkörper, die häufig auch als Abrasivstoffe bezeichnet werden. Als geeignete Reibkörper kommen beispielsweise Holzmehl, geriebener Bimsstein, Nußschalen- und/oder Pflanzenfasermahlgut, Kreide, Quarzsand und gemahlene Kunstsoffe, beispielsweise Polyethylenmehl, alleine oder in Mischung in Betracht. Typische Beispiele sind gemahlene Holzfaserstoffe (Lignocell ® BK 40/90, lichte Maschenweite 150 μm : max. 95 %), Walnußschalengranulat (UNG 300; Rettenmeier & Co., Ellwangen/FRG; Partikelbereich 170 bis 230 μm), Kreide (Cristobalitmehl -M-006®; Quarzwerke Frechen), Quarzsand F34®; Quarzwerke Frechen und/oder als Polyethylenmehl Lupo- len 1800 S P15®. Bevorzugt sind als Reibkörper Holzmehl, Quarzsand, Kreide und/oder Polyethylenmehl enthalten.Another compulsory component of hand wash pastes are friction bodies, which are often also referred to as abrasives. Suitable friction bodies include, for example, wood flour, grated pumice stone, nutshell and / or plant fiber ground material, chalk, quartz sand and ground plastics, for example polyethylene flour, alone or as a mixture. Typical examples are ground wood fiber (Lignocell ® BK 40/90, mesh size 150 μm: max. 95%), walnut shell granulate (UNG 300; Rettenmeier & Co., Ellwangen / FRG; particle range 170 to 230 μm), chalk (cristobalite flour -M -006®; Quarzwerke Frechen), quartz sand F34®; Frechen quartz movement and / or Lupolen 1800 S P15® as polyethylene flour. Wood flour, quartz sand, chalk and / or polyethylene flour are preferably contained as the friction body.
Die Reibkörper werden vorzugsweise in Mengen von 1 bis 50, bevorzugt in Mengen von 15 bis 45 Gew.-% - bezogen auf Handwaschpaste - eingesetzt. Insbesondere bei Einsatz größerer Mengen Reibkörper, vorzugsweise über 25 Gew.-%, können diese durch Zugabe von anorganischen und/oder organischen Salzen als Co-Reibkörper partiell substituiert werden. Hierfür kommen Salze wie Alkali- und/oder Erdalkalicarbonate, -sulfate-, chloride-, -hydrogencarbo- nate, -citrate und -Silikate in Betracht. Weitere zwingende Bestandteile der erfindungsgemäßen Handwaschpasten sind anionische Tenside. Typische Beispiele für anionische Tenside sind Seifen, Alkylbenzolsulfonate, Al- kansulfonate, Olefinsulfonate, Alkylethersulfonate, Glycerinethersulfonate, -Methylestersul- fonate, Sulfofettsäuren, Alkylsulfate, Fettalkoholethersulfate, Glycerinethersulfate, Fettsäu- reethersulfate, Hydroxymischethersulfate, Monoglycerid(ether)sulfate, Fettsäure- amid(ether)sulfate, Mono- und Dialkylsulfosuccinate, Mono- und Dialkylsulfosuccinamate, Sulfotriglyceride, Amidseifen, Ethercarbonsäuren und deren Salze, Fettsäureisethionate, Fett- säuresarcosinate, Fettsäuretauride, N-Acylaminosäuren, wie beispielsweise Acyllactylate, Acyltartrate, Acylglutamate und Acylaspartate, Alkyloligoglucosidsulfate, Proteinfettsäurekondensate (insbesondere pflanzliche Produkte auf Weizenbasis) und Alkyl(ether)phosphate. Sofern die anionischen Tenside Polyglycoletherketten enthalten, können diese eine konventionelle, vorzugsweise jedoch eine eingeengte Homologenverteilung aufweisen. Die anionischen Tenside sind vorzugsweise in Mengen von 1 bis 30 Gew.-%, bevorzugt von 5 bis 25 Gew.-% - bezogen auf Handwaschpaste - enthalten.The friction bodies are preferably used in amounts of 1 to 50, preferably in amounts of 15 to 45% by weight, based on the hand washing paste. In particular when larger quantities of friction bodies are used, preferably over 25% by weight, these can be partially substituted as co-friction bodies by adding inorganic and / or organic salts. Salts such as alkali and / or alkaline earth carbonates, sulfates, chlorides, hydrogen carbonates, citrates and silicates are suitable for this purpose. Other mandatory components of the hand wash pastes according to the invention are anionic surfactants. Typical examples of anionic surfactants are soaps, alkylbenzenesulfonates alkanesulfonates, Al, sulfonates olefin sulfonates, alkyl ether sulfonates, glycerol ether, -Methylestersul-, sulfofatty acids, alkyl sulfates, fatty alcohol ether sulfates, Glycerol ether, fatty reethersulfate, Hydroxymischethersulfate, monoglyceride (ether) sulfates, fatty acid amide (ether ) sulfates, mono- and dialkylsulfosuccinates, mono- and dialkylsulfosuccinamates, sulfotriglycerides, amide soaps, ether carboxylic acids and their salts, fatty acid isethionates, fatty acid sarcosinates, fatty acid taurides, N-acylamino acids, such as, for example, acyl lactylates, acyl sulfate acetic acid, acyl glucosate famates Wheat-based products) and alkyl (ether) phosphates. If the anionic surfactants contain polyglycol ether chains, they can have a conventional, but preferably a narrow, homolog distribution. The anionic surfactants are preferably present in amounts of 1 to 30% by weight, preferably 5 to 25% by weight, based on handwashing paste.
Bevorzugt im Sinne der Erfindung sind als anionische Tenside Fettalkoholsulfate und/oder Fettalkoholethersulfate enthalten.For the purposes of the invention, fatty alcohol sulfates and / or fatty alcohol ether sulfates are preferably present as anionic surfactants.
Unter Fettalkoholsulfaten sind die Sulfatierungsprodukte primärer Alkohole zu verstehen, die der Formel (II) folgen,Fatty alcohol sulfates are to be understood as meaning the sulfation products of primary alcohols which follow the formula (II)
R4O-SO3X (II)R 4 O-SO 3 X (II)
in der R4 für einen linearen oder verzweigten, aliphatischen Alkyl- und/oder Alkenylrest mit 6 bis 22, vorzugsweise 12 bis 18 Kohlenstoffatomen und X für ein Alkyl- und/oder Erdalkalimetall, Ammonium, Alkylarnmonium, Alkanolammonium oder Glucammonium steht. Typische Beispiele für Fettalkoholsulfate, die im Sinne der Erfindung Anwendung finden können, sind die Sulfatierungsprodukte von Capronalkohol, Caprylalkohol, Caprinalkohol, 2- Ethylhexylalkohol, Laurylalkohol, Myristylalkohol, Cetylalkohol, Palmoleylalkohol, Stea- rylalkohol, Isostearylalkohol, Oleylalkohol, Elaidylalkohol, Petroselinylalkohol, Arachylal- kohol, Gadoleylalkohol, Behenylalkohol und Erucylalkohol sowie deren technischen Gemischen, die durch Hochdruckhydrierung technischer Methylesterfraktionen oder Aldehyden aus der Roelen' sehen Oxosynthese erhalten werden. Die Sulfatierungsprodukte können vorzugsweise in Form ihrer Alkalisalze, und insbesondere ihrer Natriumsalze eingesetzt werden. Besonders bevorzugt sind Alkylsulfate auf Basis von C]2.18-Fettalkoholschnitten in Form ihrer Natriumsalze.in which R 4 represents a linear or branched, aliphatic alkyl and / or alkenyl radical having 6 to 22, preferably 12 to 18 carbon atoms and X represents an alkyl and / or alkaline earth metal, ammonium, alkylammonium, alkanolammonium or glucammonium. Typical examples of fatty alcohol sulfates which can be used in the context of the invention are the sulfation products of capron alcohol, caprylic alcohol, capric alcohol, 2-ethylhexyl alcohol, lauryl alcohol, myristyl alcohol, cetyl alcohol, palmoleyl alcohol, stearyl alcohol, isostearyl alcohol, oleyl alcohol, aridyl alcohol, arachidyl alcohol, elaidol alcohol, elaid alcohol alcohol, gadoleyl alcohol, behenyl alcohol and erucyl alcohol and their technical mixtures, which are characterized by high-pressure hydrogenation of technical methyl ester fractions or aldehydes the Roelen 'see oxosynthesis can be obtained. The sulfation products can preferably be used in the form of their alkali metal salts, and in particular their sodium salts. Alkyl sulfates based on C ] 2 are particularly preferred. 18 fatty alcohol cuts in the form of their sodium salts.
Die Fettalkoholsulfate sind vorzugsweise in Mengen von 5 bis 25, bevorzugt von 10 bis 20 Gew.-% - berechnet als Aktivsubstanzgehalt und bezogen auf Handwaschpaste - enthalten.The fatty alcohol sulfates are preferably present in amounts of 5 to 25% by weight, preferably 10 to 20% by weight, calculated as the active substance content and based on handwashing paste.
Gemäß der vorliegenden Erfindung können als alleiniges anionisches Tensid Fettalkoholethersulfate enthalten sein, vorzugsweise sind sie in Mischung mit den schon beschriebenen Fettalkoholsulfaten enthalten. Die Fettalkoholethersulfate sind vorzugsweise in Mengen von 0 bis 5 Gew.-%, bevorzugt in Mengen von 0 bis 3 Gew.-% - berechnet als Aktivsubstanzgehalt und bezogen auf Handwaschpaste - enthalten. Fettalkoholethersulfate ("Ethersulfate") stellen bekannte anionische Tenside dar, die großtechnisch durch SO3- oder CSA-Sulfatierung von Fettalkoholpolyglycolethern und nachfolgende Neutralisation hergestellt werden. Im Sinne der Erfindung kommen Ethersulfate in Betracht, die der Formel (III) folgen,According to the present invention, fatty alcohol ether sulfates can be present as the sole anionic surfactant, preferably they are contained in a mixture with the fatty alcohol sulfates already described. The fatty alcohol ether sulfates are preferably present in amounts of 0 to 5% by weight, preferably in amounts of 0 to 3% by weight, calculated as the active substance content and based on handwashing paste. Fatty alcohol ether sulfates ("ether sulfates") are known anionic surfactants which are produced on an industrial scale by SO 3 or CSA sulfation of fatty alcohol polyglycol ethers and subsequent neutralization. For the purposes of the invention, ether sulfates which follow the formula (III) are suitable
R5O-(CH2CH2O),SO3X (III)R 5 O- (CH 2 CH 2 O), SO 3 X (III)
in der R5 für einen linearen oder verzweigten Alkyl- und/oder Alkenylrest mit 6 bis 22 Kohlenstoffatomen, 1 für Zahlen von 1 bis 10 und X für ein Alkali- und/oder Erdalkalimetall, Ammonium, Alkylammonium, Alkanolammonium oder Glucammonium steht.in which R 5 represents a linear or branched alkyl and / or alkenyl radical with 6 to 22 carbon atoms, 1 for numbers from 1 to 10 and X for an alkali and / or alkaline earth metal, ammonium, alkylammonium, alkanolammonium or glucammonium.
Typische Beispiele sind die Sulfate von Anlagerungsprodukten von durchschnittlich 1 bis 10 und insbesondere 2 bis 5 Mol Ethylenoxid an Capronalkohol, Caprylalkohol, 2-Ethylhexylal- kohol, Caprinalkohol, Laurylalkohol, Isotridecylalkohol, Myristylalkohol, Cetylalkohol, Pal- moleylalkohol, Stearylalkohol, Isostearylalkohol, Oleylalkohol, Elaidylalkohol, Petrose- linylalkohol, Arachylalkohol, Gadoleylalkohol, Behenylalkohol und Erucylalkohol sowie deren technische Mischungen, in Form ihrer Natrium- und/oder Magnesiumsalze. Die Ethersulfate können dabei sowohl eine konventionelle als auch eine eingeengte Homologenverteilung aufweisen. Besonders bevorzugt ist der Einsatz von Ethersulfaten auf Basis von Addukten von im Mittel 2 bis 3 Mol Ethylenoxid an technische CI2/I4- bzw. C12/]8-Kokosfettalkoholfrak- tionen in Form ihrer Natrium- und/ oder Magnesiumsalze.Typical examples are the sulfates of addition products with an average of 1 to 10 and in particular 2 to 5 mol ethylene oxide onto capron alcohol, caprylic alcohol, 2-ethylhexyl alcohol, capric alcohol, lauryl alcohol, isotridecyl alcohol, myristyl alcohol, cetyl alcohol, palmoleyl alcohol, stearyl alcohol, isostyl alcohol, isostearyl alcohol Elaidyl alcohol, petroseline alcohol, arachyl alcohol, gadoleyl alcohol, behenyl alcohol and erucyl alcohol and their technical mixtures, in the form of their sodium and / or magnesium salts. The ether sulfates can have both a conventional and a narrow homolog distribution. The use of ether sulfates based on adducts is particularly preferred of on average 2 to 3 moles of ethylene oxide with technical C I2 / I4 - or C 12 /] 8 -Kokosfettalkoholfrak- functions in the form of their sodium and / or magnesium salts.
Fakultativ können die erfindungsgemäßen Handwaschpasten weitere nichtionische Tenside enthalten, wobei die Partilaglyceride nicht unter den weiteren nichtionischen Tensiden sub- sumiert werden. Typische Beispiele für weitere nichtionische Tenside sind Fettalkoholpolyglycolether, Alkylphenolpolyglycolether, Fettsäurepolyglycolester, Fettsäureamidpolygly- colether, Fettaminpolyglycolether, alkoxylierte Triglyceride, Mischether bzw. Mischformale, gegebenenfalls partiell oxidierte Alk(en)yloligoglykoside bzw. Glucoronsäurederivate, Fett- säure-N-alkylglucamide, Proteinhydrolysate (insbesondere pflanzliche Produkte auf Weizenbasis), Polyolfettsäureester, Zuckerester, Sorbitanester, Polysorbate und Aminoxide. Sofern die nichtionischen Tenside Polyglycoletherketten enthalten, können diese eine konventionelle, vorzugsweise jedoch eine eingeengte Homologenverteilung aufweisen. Bevorzugt sind als weitere nichtionische Tenside Fettalkoholpolyglycolether und/oder Alk(en)yloligoglykoside enthalten.The handwashing pastes according to the invention can optionally contain further nonionic surfactants, the particle glycerides not being added to the other nonionic surfactants. Typical examples of further nonionic surfactants are fatty alcohol polyglycol ethers, alkylphenol polyglycol ethers, fatty acid polyglycol esters, fatty acid amide polyglycol ethers, fatty amine polyglycol ethers, alkoxylated triglycerides, mixed ethers or mixed formals, optionally partially oxidized alk (en) yl oligoglycosides, in particular -glycosyl glucosilicate acid derivatives (GLC), glucorosulfonic acid derivatives (F) vegetable products based on wheat), polyol fatty acid esters, sugar esters, sorbitan esters, polysorbates and amine oxides. If the nonionic surfactants contain polyglycol ether chains, they can have a conventional, but preferably a narrow, homolog distribution. Fatty alcohol polyglycol ethers and / or alk (en) yl oligoglycosides are preferably contained as further nonionic surfactants.
Fettalkoholpolyglycolether stellen bekannte nichtionische Tenside dar, die großtechnisch durch Alkoxylierung von Fettalkoholen in Gegenwart von sauren, vorzugsweise jedoch alkalischen Katalysatoren hergestellt werden. Dabei kann es sich bei den Polyglycolethern um Ethylenoxid (EO)-, Propylenoxid (PO)- oder EO/PO-Addukte - letztere mit Random- oder Blockverteilung - handeln. Im Sinne der Erfindung kommen Fettalkoholpolyglycolether der Formel (IV) in Betracht,Fatty alcohol polyglycol ethers are known nonionic surfactants which are produced on an industrial scale by alkoxylation of fatty alcohols in the presence of acidic, but preferably alkaline, catalysts. The polyglycol ethers can be ethylene oxide (EO), propylene oxide (PO) or EO / PO adducts - the latter with random or block distribution. For the purposes of the invention, fatty alcohol polyglycol ethers of the formula (IV) are suitable
R6O-(CH2CH2O)z H (IV)R 6 O- (CH 2 CH 2 O) z H (IV)
in der R6 für einen linearen oder verzweigten Alkyl- und/oder Alkenylrest mit 6 bis 22 Kohlenstoffatomen und z für Zahlen von 1 bis 10 steht.in which R 6 represents a linear or branched alkyl and / or alkenyl radical having 6 to 22 carbon atoms and z represents numbers from 1 to 10.
Typische Beispiele sind Anlagerungsprodukte von durchschnittlich 1 bis 10 und insbesondere 3 bis 7 Mol Ethylenoxid an Capronalkohol, Caprylalkohol, 2-Ethylhexylalkohol, Caprinal- kohol, Laurylalkohol, Isotridecylalkohol, Myristylalkohol, Cetylalkohol, Palmoleylalkohol, Stearylalkohol, Isostearylalkohol, Oleylalkohol, Elaidylalkohol, Petroselinylalkohol, Arachyl- alkohol, Gadoleylalkohol, Behenylalkohol und Erucylalkohol sowie deren technische Mi- schungen, in Form ihrer Natrium- und/oder Magnesiumsalze. Die Polyglycolether können dabei sowohl eine konventionelle als auch eine eingeengte Homologenverteilung aufweisen. Besonders bevorzugt ist der Einsatz von Addukten von durchschnittlich 3 bis 7 Mol Ethylenoxid an technische Kokosfettalkohol- bzw. Oleylalkoholfraktionen.Typical examples are addition products of an average of 1 to 10 and in particular 3 to 7 mol of ethylene oxide with capron alcohol, caprylic alcohol, 2-ethylhexyl alcohol, capric alcohol, lauryl alcohol, isotridecyl alcohol, myristyl alcohol, cetyl alcohol, palmoleyl alcohol, stearyl alcohol, isostearyl alcohol, elaalyl alcohol, oleyl alcohol, oleyl alcohol - alcohol, gadoleyl alcohol, behenyl alcohol and erucyl alcohol and their technical mix in the form of their sodium and / or magnesium salts. The polyglycol ethers can have both a conventional and a narrow homolog distribution. The use of adducts of an average of 3 to 7 moles of ethylene oxide with technical coconut oil alcohol or oleyl alcohol fractions is particularly preferred.
Alkyl- und Alkenyloligoglykoside stellen bekannte Stoffe dar, die nach den einschlägigen Verfahren der präparativen organischen Chemie erhalten werden können und der Formel (V) folgen,Alkyl and alkenyl oligoglycosides are known substances which can be obtained by the relevant processes in preparative organic chemistry and follow the formula (V),
R7O-[G], (V)R 7 O- [G], (V)
in der R7 für einen Alkyl- und oder Alkenylrest mit 4 bis 22 Kohlenstoffatomen, G für einen Zuckerrest mit 5 oder 6 Kohlenstoffatomen und q für eine Zahl von 1 bis 10 steht. Die Alkyl- und/oder Alkenyloligoglykoside können sich von Aldosen bzw. Ketosen mit 5 oder 6 Kohlenstoffatomen, vorzugsweise der Glucose ableiten. Die bevorzugten Alkyl- und/oder Alkenyloligoglykoside sind somit Alkyl- und/oder Alkenyloligoglucoside.in which R 7 represents an alkyl and or alkenyl radical having 4 to 22 carbon atoms, G represents a sugar radical having 5 or 6 carbon atoms and q represents a number from 1 to 10. The alkyl and / or alkenyl oligoglycosides can be derived from aldoses or ketoses with 5 or 6 carbon atoms, preferably glucose. The preferred alkyl and / or alkenyl oligoglycosides are thus alkyl and / or alkenyl oligoglucosides.
Die Indexzahl q in der allgemeinen Formel (V) gibt den Oligomerisierungsgrad (DP-Grad), d. h. die Verteilung von Mono- und Oligoglykosiden an und steht für eine Zahl zwischen 1 und 10. Während q in einer gegebenen Verbindung stets ganzzahlig sein muß und hier vor allem die Werte q = 1 bis 6 annehmen kann, ist der Wert q für ein bestimmtes Alkyloligoglykosid eine analytisch ermittelte rechnerische Größe, die meistens eine gebrochene Zahl darstellt. Vorzugsweise werden Alkyl- und/oder Alkenyloligoglykoside mit einem mittleren Oligomerisierungsgrad q von 1,1 bis 3,0 eingesetzt. Aus anwendungstechnischer Sicht sind solche Alkyl- und/oder Alkenyloligoglykoside bevorzugt, deren Oligomerisierungsgrad kleiner als 1,7 ist und insbesondere zwischen 1,2 und 1,4 liegt.The index number q in the general formula (V) indicates the degree of oligomerization (DP degree), i.e. H. the distribution of mono- and oligoglycosides is present and stands for a number between 1 and 10. While q must always be an integer in a given compound and here can take on the values q = 1 to 6, the value q is for a certain alkyl oligoglycoside an analytically calculated quantity, which usually represents a fractional number. Alkyl and / or alkenyl oligoglycosides with an average degree of oligomerization q of 1.1 to 3.0 are preferably used. From an application point of view, preference is given to those alkyl and / or alkenyl oligoglycosides whose degree of oligomerization is less than 1.7 and in particular between 1.2 and 1.4.
Der Alkyl- bzw. Alkenylrest R7 kann sich von primären Alkoholen mit 8 bis 16, vorzugsweise 8 bis 14 Kohlenstoffatomen ableiten. Typische Beispiele sind Caprylalkohol, Caprinalkohol, Undecylalkohol Laurylalkohol, Myristylalkohol, Cetylalkohol, Palmoleylalkohol sowie deren technische Mischungen, wie sie beispielsweise bei der Hydrierung von technischen Fettsäure- methylestern oder im Verlauf der Hydrierung von Aldehyden aus der Roelen'schen Oxosyn- these anfallen.The alkyl or alkenyl radical R 7 can be derived from primary alcohols having 8 to 16, preferably 8 to 14, carbon atoms. Typical examples are caprylic alcohol, capric alcohol, undecyl alcohol, lauryl alcohol, myristyl alcohol, cetyl alcohol, palmoleyl alcohol and their technical mixtures, such as those used in the hydrogenation of technical fatty acid methyl esters or in the course of the hydrogenation of aldehydes from Roelen's oxosynthesis.
Die nichtionischen Tenside, insbesondere die Alk(en)yloligoglucoside, sind vorzugsweise in Mengen von 0 bis 20 Gew.-%, bevorzugt in Mengen von 0,1 bis 10 Gew.-% - berechnet als Aktivsubstanzgehalt und bezogen auf Handwaschpaste - enthalten.The nonionic surfactants, in particular the alk (en) yl oligoglucosides, are preferably present in amounts of 0 to 20% by weight, preferably in amounts of 0.1 to 10% by weight, calculated as the active substance content and based on hand washing paste.
Fakultativ können die erfindungsgemäßen Handwaschpasten zwitterionische bzw. ampholy- tische Tenside enthalten. Typische Beispiele für amphotere bzw. zwitterionische Tenside sind Alkylbetaine, Alkylamidobetaine, Aminopropionate, Aminoglycinate, Imidazoliniumbe- taine und Sulfobetaine. Bei den genannten Tensiden handelt es sich ausschließlich um bekannte Verbindungen. Bevorzugt sind als zwitterionische bzw. ampholytische Tenside Alkylbetaine und/oder Alkylamidobetaine enthalten.The hand washing pastes according to the invention can optionally contain zwitterionic or ampholytic surfactants. Typical examples of amphoteric or zwitterionic surfactants are alkyl betaines, alkyl amido betaines, aminopropionates, aminoglycinates, imidazolinium betaines and sulfobetaines. The surfactants mentioned are exclusively known compounds. Alkyl betaines and / or alkyl amido betaines are preferably contained as zwitterionic or ampholytic surfactants.
Betaine stellen bekannte Tenside dar, die überwiegend durch Carboxyalkylierung, vorzugsweise Carboxymethylierung von aminischen Verbindungen hergestellt werden. Vorzugsweise werden die Ausgangsstoffe mit Halogencarbonsäuren oder deren Salzen, insbesondere mit Natriumchloracetat kondensiert, wobei pro Mol Betain ein Mol Salz gebildet wird. Ferner ist auch die Anlagerung von ungesättigten Carbonsäuren wie beispielweise Acrylsäure möglich. Zur Nomenklatur und insbesondere zur Unterscheidung zwischen Betainen und "echten" Am- photensiden sei auf den Beitrag von U.Ploog in Seifen-Öle- Fette-Wachse, 198, 373 (1982) verwiesen. Weitere Übersichten zu diesem Thema finden sich beispielsweise von A.O'Lennick et al. in HAPPI, Nov. 70 (1986), S.Holzman et al. in Tens.Det. 23, 309 (1986), R.Bibo et al. in Soap Cosm.Chem.Spec. Apr. 46 (1990) und P.Ellis et al. in Euro Cosm. 1_, 14 (1994).Betaines are known surfactants which are predominantly produced by carboxyalkylation, preferably carboxymethylation, of aminic compounds. The starting materials are preferably condensed with halocarboxylic acids or their salts, in particular with sodium chloroacetate, one mol of salt being formed per mole of betaine. Furthermore, the addition of unsaturated carboxylic acids such as acrylic acid is also possible. Regarding the nomenclature and in particular the distinction between betaines and "real" amphoteric surfactants, reference is made to the contribution by U.Ploog in Seifen-Öle-Fette-Wwachs, 198, 373 (1982). Further overviews on this topic can be found for example by A. O'Lennick et al. in HAPPI, Nov. 70 (1986), S. Holzman et al. in Tens.Det. 1986, 23: 309, R.Bibo et al. in Soap Cosm.Chem.Spec. Apr. 46 (1990) and P.Ellis et al. in Euro Cosm. 1_, 14 (1994).
Beispiele für geeignete Betaine stellen die Carboxyalkylierungsprodukte von sekundären und insbesondere tertiären Aminen dar, die der Formel (VI) folgen,Examples of suitable betaines are the carboxyalkylation products of secondary and in particular tertiary amines which follow the formula (VI)
R9 R 9
R8-N-(CH2)b COOY (VI)R 8 -N- (CH 2 ) b COOY (VI)
R I 10 in der R8 für Alkyl- und oder Alkenylreste mit 6 bis 22 Kohlenstoffatomen, R9 für Wasserstoff oder Alkylreste mit 1 bis 4 Kohlenstoffatomen, R10 für Alkylreste mit 1 bis 4 Kohlenstoffatomen, b für Zahlen von 1 bis 6 und Y für ein Alkali- und/oder Erdalkalimetall oder Ammonium steht. R I 10 in which R 8 stands for alkyl and or alkenyl residues with 6 to 22 carbon atoms, R 9 stands for hydrogen or alkyl residues with 1 to 4 carbon atoms, R 10 stands for alkyl residues with 1 to 4 carbon atoms, b stands for numbers from 1 to 6 and Y for an alkali - And / or alkaline earth metal or ammonium.
Typische Beispiele sind die Carboxymethylierungsprodukte von Hexylmethylamin, Hexyldi- methylamin, Octyldimethylamin, Decyldimethylamin, Dodecylmethylamin, Dodecyldime- thylamin, Dodecylethylmethylarnin, C12/14-Kokosalkyldimethylamin, Myristyldimethylamin, Cetyldimethylamin, Stearyldimethylamin, Stearylethylmethylamin, Oleyldimethylamin, C16/18-Talgalkyldimethylamin sowie deren technische Gemische.Typical examples are the carboxymethylation products of hexylmethylamine methylamine, Hexyldi-, octyldimethylamine, decyldimethylamine, dodecylmethylamine, Dodecyldime- methylamine, Dodecylethylmethylarnin, C 12/14 -Kokosalkyldimethylamin, myristyldimethylamine, cetyldimethylamine, stearyldimethylamine, stearyl, oleyl, C 16/18 tallow alkyl dimethyl amine, and their technical Mixtures.
Weiterhin kommen auch Carboxyalkylierungsprodukte von Amidoaminen in Betracht, die der Formel (VII) folgen,Carboxyalkylation products of amidoamines which follow the formula (VII) are also suitable,
R9 R 9
II.
RuCO-NH-(CH2)a -N-(CH2)bCOOY (VII)R u CO-NH- (CH 2 ) a -N- (CH 2 ) b COOY (VII)
R I .o R I .o
in der RuCO für einen aliphatischen Acylrest mit 6 bis 22 Kohlenstoffatomen und 0 oder 1 bis 3 Doppelbindungen, a für Zahlen von 1 bis 3 steht und R9, R10, b und Y die oben angegebenen Bedeutungen haben.in which R u CO is an aliphatic acyl radical having 6 to 22 carbon atoms and 0 or 1 to 3 double bonds, a is a number from 1 to 3 and R 9 , R 10 , b and Y have the meanings given above.
Typische Beispiele sind Umsetzungsprodukte von Fettsäuren mit 6 bis 22 Kohlenstoffatomen, namentlich Capronsäure, Caprylsäure, Caprinsäure, Laurinsäure, Myristinsäure, Palmitinsäu- re, Palmoleinsäure, Stearinsäure, Isostearinsäure, Ölsäure, Elaidinsäure, Petroselinsäure, Li- nolsäure, Linolensäure, Elaeostearinsäure, Arachinsäure, Gadoleinsäure, Behensäure und Erucasäure sowie deren technische Gemische, mit N,N-Dimethylaminoethylamin, N,N-Di- methylaminopropylamin, N,N-Diethylaminoethylamin und N,N-Diethylaminopropylamin, die mit Natriumchloracetat kondensiert werden. Bevorzugt ist der Einsatz eines Kondensationsproduktes von Cg/ls-Kokosfettsäure-N,N- dimethylaminopropylamid mit Natriumchloracetat. Die zwitterionischen bzw. ampholytischen Tenside sind vorzugsweise in Mengen von 0 bis 30, bevorzugt von 0,1 bis 20 - berechnet als Aktivsubstanzgehalt und bezogen auf Handwaschpaste - enthalten.Typical examples are reaction products of fatty acids with 6 to 22 carbon atoms, namely caproic acid, caprylic acid, capric acid, lauric acid, myristic acid, palmitic acid, palmoleic acid, stearic acid, isostearic acid, oleic acid, elaidic acid, petroselinic acid, linoleic acid, linolenic acid, arenachic acid, gadeleostearic acid, gaoleostolic acid , Behenic acid and erucic acid and their technical mixtures, with N, N-dimethylaminoethylamine, N, N-dimethylaminopropylamine, N, N-diethylaminoethylamine and N, N-diethylaminopropylamine, which are condensed with sodium chloroacetate. It is preferred to use a condensation product of C g / ls coconut fatty acid N, N-dimethylaminopropylamide with sodium chloroacetate. The zwitterionic or ampholytic surfactants are preferably present in amounts from 0 to 30, preferably from 0.1 to 20, calculated as the active substance content and based on hand washing paste.
Die erfindungsgemäßen Handwaschpasten können ferner typische Zusatzstoffe in üblichen Mengen enthalten. Typische Zusatzstoffe sind Fettsäuren, Schaumbooster, Farbstoffe, Duft- stoffe, pH-Wert-Regulantien, Emulgatoren, Konservierungsstoffe, Sequestrierungsmittel sowie ggf. Schaumregulatoren.The hand wash pastes according to the invention can furthermore contain typical additives in customary amounts. Typical additives are fatty acids, foam boosters, dyes, fragrances, pH regulators, emulsifiers, preservatives, sequestering agents and possibly foam regulators.
Als Fettsäuren eignen sich Carbonsäuren mit 10 bis 22 Kohlenwasserstoffatomen, die vorzugsweise gesättigt sind. Ein typisches Beispiel ist gehärtete Tranfettsäure. Derartige Fettsäuren können in Mengen von 0 bis 10 Gew.-%, vorzugsweise in Mengen von 0 bis 2 Gew.-%Suitable fatty acids are carboxylic acids with 10 to 22 hydrocarbon atoms, which are preferably saturated. A typical example is hydrogenated trans fatty acid. Such fatty acids can be present in amounts of 0 to 10% by weight, preferably in amounts of 0 to 2% by weight.
- bezogen auf Handwaschpaste - enthalten sein.- based on handwashing paste.
Typische Beispiele für geeignete O/W- bzw. W/O-Emulgatoren sind gehärtetes und ethoxy- liertes Ricinusöl, Polyglycerinfettsäureester oder Polyglycerinpolyricinoleate. Derartige Emulgatoren können in Mengen von 0 bis 5 Gew.-%, vorzugsweise 0 bis 2 Gew.-% - bezogen auf Handwaschpaste - enthalten sein. Als Schaumbooster eignen sich z.B. Fettsäurealkanol- amide, insbesondere Kokosfettsäurediethanolamid. Die Schaumbooster können in Mengen von 0 bis 3, vorzugsweise in Mengen von 0,1 bis 1,5 Gew.-% - bezogen auf HandwaschpasteTypical examples of suitable O / W or W / O emulsifiers are hardened and ethoxylated castor oil, polyglycerol fatty acid esters or polyglycerol polyricinoleates. Such emulsifiers can be present in amounts of 0 to 5% by weight, preferably 0 to 2% by weight, based on handwashing paste. Suitable foam boosters are e.g. Fatty acid alkanol amides, especially coconut fatty acid diethanolamide. The foam boosters can be used in amounts of 0 to 3, preferably in amounts of 0.1 to 1.5% by weight, based on hand washing paste
- enthalten sein.- be included.
Geeignete Sequestrierungsmittel sind beispielsweise in der schon zitierten europäischen Of- fenlegungsschrift EP-A- 881 281 ausführlich offenbart worden.Suitable sequestering agents have been disclosed in detail, for example, in the European patent application EP-A-881 281 already cited.
Mittels pH-Wert-Regulantien kann der pH- Wert der Handwaschpasten eingestellt werden. Werden besonders hautmilde Mittel gewünscht, empfehlen sich pH- Werte zwischen 4,0 und 9, vorzugsweise zwischen 5,5 und 8. Zur Entfernung hartnäckiger Verschmutzungen empfiehlt es sich, die Mittel alkalischer einzustellen auf pH- Werte von 8 bis 14, vorzugsweise von 9,5 bis 11. Zur Einstellung eignen sich die bekannten wasserlöslichen Hydroxide, insbesondere Natriumhydroxid. Falls gewünscht kann der pH- Wert auch mittels eines Puffersystems eingestellt werden. Als Konservierungsmittel sind beispielsweise Aldehyde wie Benzaldehyd oder Benzylalkohol geeignet, die vorzugsweise in Mengen bis 1 Gew.-% enthalten sind.The pH value of the handwashing pastes can be adjusted using pH regulators. If particularly mild agents are desired, pH values between 4.0 and 9, preferably between 5.5 and 8 are recommended. To remove stubborn dirt, it is recommended to adjust the agents more alkaline to pH values from 8 to 14, preferably from 9 , 5 to 11. The known water-soluble hydroxides, in particular sodium hydroxide, are suitable for adjustment. If desired, the pH can also be adjusted using a buffer system. Suitable preservatives are, for example, aldehydes such as benzaldehyde or benzyl alcohol, which are preferably present in amounts of up to 1% by weight.
Der zu ad 100 Gew.-% fehlende Rest der Handwaschpasten ist Wasser ggf. in Mischung mit weiteren anderen wasserlöslichen Lösungsmitteln, vorzugsweise Wasser alleine. Der Wassergehalt der Pasten liegt vorzugsweise im Bereich von 20 bis 60, bevorzugt 25 bis 55 Gew.- %, bezogen auf Handwaschpaste.The remaining 100% by weight of the rest of the handwashing pastes is water, possibly in a mixture with other other water-soluble solvents, preferably water alone. The water content of the pastes is preferably in the range from 20 to 60, preferably 25 to 55% by weight, based on hand-washing paste.
Die erfindungsgemäßen Handwaschpasten können auf übliche Weise durch Vermischen der Komponenten, wobei die tensidischen Komponenten meist als wäßrige Paste eingebracht werden, hergestellt werden. In der Regel wird die berechnete Menge Wasser vorgelegt und hierin das anionische Tensid, vorzugsweise bei leicht erhöhten Temperaturen von etwa 60 bis 100 °C, gelöst. Dazu werden die Partialglyceride sowie ggf. weitere Tenside und übliche Bestandteile eingerührt. Nach Abkühlung auf Temperaturen von ca. 20 bis 40 °C werden die Reibkörper eingearbeitet und abschließend durch Zugabe der pH-Wert-Regulantien der gewünschte pH- Wert eingestellt.The handwashing pastes according to the invention can be produced in the usual way by mixing the components, the surfactant components usually being introduced as an aqueous paste. As a rule, the calculated amount of water is introduced and the anionic surfactant is dissolved therein, preferably at slightly elevated temperatures of about 60 to 100 ° C. For this purpose, the partial glycerides as well as any other surfactants and usual constituents are stirred in. After cooling to temperatures of approx. 20 to 40 ° C, the friction bodies are incorporated and finally the desired pH value is set by adding the pH value regulators.
Die erfindungsgemäßen Handwaschpasten erzeugen beim Anwender ein angenehmes Hautgefühl beim Waschen, das als glatter und weniger reibend und kratzend empfunden wird. Zusätzlich wird der bei der Anwendung erzeugte Schaum als cremig und feinporig empfunden.The handwashing pastes according to the invention produce a pleasant feeling on the skin when washing, which is perceived as smoother and less rubbing and scratching. In addition, the foam generated during use is felt to be creamy and fine-pored.
Ein weiterer Gegenstand der vorliegenden Erfindung betrifft daher die Verwendung von Par- tialglyceriden zur Verbesserung des Hautgefühls und der Schaumentwicklung von Handwaschpasten. Another object of the present invention therefore relates to the use of partial glycerides to improve the feeling on the skin and the foaming of hand wash pastes.
B e i s p i e l eB e i s p i e l e
Die Handwaschpasten wurden hergestellt durch Verrühren der in Tabelle 1 angegebenen Verbindungen in den dort wiedergegebenen Mengenverhältnissen:The handwashing pastes were prepared by stirring the compounds listed in Table 1 in the proportions shown there:
Tabelle 1Table 1
LegendeLegend
1 = Sulfopon HC®; Handelsprodukt der Henkel KGaA; Aktivsubstanzgehalt ca. 65 Gew.-%1 = Sulfopon HC®; Commercial product from Henkel KGaA; Active substance content approx. 65% by weight
2 = Lamesoft PO 65®; Handelsprodukt der Henkel KGaA; Aktivsubstanzgehalt ca. 65 Gew.-%2 = Lamesoft PO 65®; Commercial product from Henkel KGaA; Active substance content approx. 65% by weight
3 = Glucopon 650 EC® ;Handelsprodukt der Henkel KGaA; Aktivsubstanzgehalt ca. 51 Gew.-%3 = Glucopon 650 EC®; commercial product from Henkel KGaA; Active substance content approx. 51% by weight
4 = Dimethyl-N-(C8-18-kokosamidopropyl)ammoniumacetobetain N,N-; Dehyton K®; Handelsprodukt der Henkel KGaA; Aktivsubstanzgehalt ca. 30 Gew.-%4 = dimethyl-N- (C8-18-cocosamidopropyl) ammonium acetobetaine N, N-; Dehyton K®; Commercial product from Henkel KGaA; Active substance content approx. 30% by weight
5 = Laurylethersulfat mit 3 EO, Na-Salz; Texapon NSO®; Handelsprodukt der Henkel KGaA; Aktivsubstanzgehalt ca. 27 Gew.-%5 = lauryl ether sulfate with 3 EO, Na salt; Texapon NSO®; Commercial product from Henkel KGaA; Active substance content approx. 27% by weight
6 = Konservierungsmittel von Isothiazolinon-Typ; Handelsprodukt der Fa. Thor Die Handwaschpasten wurden von 10 Anwendern im Vergleich zu üblichen auf dem Markt befindlichen Produkten getestet (Anschmutzung: eine Mischung aus Pigmentruß und pflanzlichen Ölen gemäß dem IPP-Test (Test für den Industrieverband von Putz- und Pflegemitteln) nach Gardner). Nach subjektivem Empfinden fanden 8 bzw. 9 der 10 Anwender das Hautge- fühl besser; auch die Schaumbeschaffenheit wurde von den gleichen Anwendern als deutlich besser, weil cremiger und feinporiger, eingestuft. Als Vergleich dienten ein Handelsprodukt 1 (mit Holzmehl), welches nach eigenen Angaben Aqua, Lignum, Sodium Tallow Sulfate, So- dium Lauryl Sulfate, Sodium C14-17 Alkyl See Sulfonate; Cocoamidopropyl Betaine, Cellu- lose Gum; Soyamide DEA; Sodium Citrate; Parfüm; Citric Acid; Benzyl Alcohol; Me- thylchloroisothiazolinone (INCI-Nomenklatur) enthielt. Handelsprodukt 2 ( mit Quarzsand) enthielt nach eigenen Angaben Silica, Aqua; Paraffinum Liquidum; Kaolin; Sodium carbo- nate; Oleic Acid; Palmitic Acid; Linoleic Acid; Disodium Pyrophosphate; Cocoamide DEA; Potassium Hydroxide; Triethanolamine; Cellulose Gum; Glycerin; Cocoamidopropyl Betaine; Stearic Acid; 1-Phenylethanol; Benzaldehyde (nach INCI). 6 = isothiazolinone type preservative; Commercial product from Thor The hand washing pastes were tested by 10 users in comparison to the usual products on the market (soiling: a mixture of pigment black and vegetable oils according to the IPP test (test for the industrial association of cleaning and care products according to Gardner). Subjectively, 8 and 9 of the 10 users found the skin feeling better; The foam properties were also rated as significantly better by the same users because they were creamier and more porous. A commercial product 1 (with wood flour) was used as a comparison, which according to the company stated aqua, lignum, sodium tallow sulfate, sodium lauryl sulfate, sodium C14-17 alkyl lake sulfonate; Cocoamidopropyl betaine, cellulose gum; Soyamide DEA; Sodium citrate; Perfume; Citric acid; Benzyl alcohol; Methylchloroisothiazolinone (INCI nomenclature) contained. Commercial product 2 (with quartz sand) contained, according to its own information, silica, aqua; Paraffinum liquidum; Kaolin; Sodium carbonate; Oleic acid; Palmitic acid; Linoleic acid; Disodium pyrophosphate; Cocoamide DEA; Potassium hydroxide; Triethanolamines; Cellulose gum; Glycerin; Cocoamidopropyl betaines; Stearic acid; 1-phenylethanol; Benzaldehydes (according to INCI).
Claims
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19916036.8 | 1999-04-09 | ||
| DE1999116036 DE19916036A1 (en) | 1999-04-09 | 1999-04-09 | Hand washing pastes |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| WO2000061709A2 true WO2000061709A2 (en) | 2000-10-19 |
| WO2000061709A3 WO2000061709A3 (en) | 2001-02-01 |
Family
ID=7904012
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/EP2000/002847 Ceased WO2000061709A2 (en) | 1999-04-09 | 2000-03-31 | Handwashing pastes |
Country Status (2)
| Country | Link |
|---|---|
| DE (1) | DE19916036A1 (en) |
| WO (1) | WO2000061709A2 (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102429833A (en) * | 2011-12-29 | 2012-05-02 | 北京绿伞化学股份有限公司 | Environment-friendly hand sanitizer and preparation method thereof |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE10257984A1 (en) * | 2002-12-12 | 2004-06-24 | Beiersdorf Ag | Cosmetic or dermatological skin cleansing agent e.g. for reducing skin roughness, comprises fatty acid salt surfactants |
| DE102007022693A1 (en) | 2007-05-11 | 2009-01-15 | Evonik Stockhausen Gmbh | Skin and hand cleaners with hydrophilic emollients |
| DE102009046272A1 (en) | 2009-11-02 | 2011-05-05 | Evonik Stockhausen Gmbh | Natural resource-based friction agent with rheology enhancing properties |
| DE102011004815A1 (en) | 2011-02-28 | 2012-08-30 | Evonik Stockhausen Gmbh | Skin and hand cleanser containing superabsorbent particles |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA1138292A (en) * | 1978-06-30 | 1982-12-28 | Johannes C.P. Schreuder | Handwashing composition |
| US4508634A (en) * | 1983-11-15 | 1985-04-02 | Minnesota Mining And Manufacturing Company | Aqueous skin cleaner composition comprising propylene carbonate |
| DE4301994C1 (en) * | 1993-01-26 | 1994-08-25 | Wella Ag | Hair and body cleansers |
| RU2044036C1 (en) * | 1993-04-26 | 1995-09-20 | Юрий Евгеньевич Мальков | Agent for dry cleansing hands |
| US5534265A (en) * | 1994-08-26 | 1996-07-09 | The Procter & Gamble Company | Thickened nonabrasive personal cleansing compositions |
| BR9604788B1 (en) * | 1995-04-04 | 2009-01-13 | stable and aqueous foaming surfactant dispersion and process for preparing it. |
-
1999
- 1999-04-09 DE DE1999116036 patent/DE19916036A1/en not_active Withdrawn
-
2000
- 2000-03-31 WO PCT/EP2000/002847 patent/WO2000061709A2/en not_active Ceased
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102429833A (en) * | 2011-12-29 | 2012-05-02 | 北京绿伞化学股份有限公司 | Environment-friendly hand sanitizer and preparation method thereof |
Also Published As
| Publication number | Publication date |
|---|---|
| DE19916036A1 (en) | 2000-10-12 |
| WO2000061709A3 (en) | 2001-02-01 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| EP0870821A1 (en) | Composition for cleaning hard surface | |
| DE4326112A1 (en) | Detergent for hard surfaces | |
| DE19906481A1 (en) | Gel-shaped detergent for flush toilets | |
| EP0796318B1 (en) | Solid pourable preparations | |
| EP1115820A1 (en) | Use of alkoxylated carboxylic acid esters for reducing viscosity of aqueous surfactant systems | |
| WO2000053718A1 (en) | Gel shaped cleaning agent for flush toilets | |
| EP1137750A1 (en) | General purpose cleaners | |
| DE19830267A1 (en) | Hand dishwashing liquid | |
| WO2000061709A2 (en) | Handwashing pastes | |
| WO1999010461A1 (en) | Heavily foaming detergent mixtures containing fatty acid polyglycol ester sulphates | |
| EP1007619A1 (en) | Hard soap containing fatty acid polyglycol ester sulphates | |
| EP0863972A1 (en) | Aqueous surfactant mixture | |
| DE19641277C2 (en) | Syndet soaps | |
| DE19813059C2 (en) | Aqueous agents for cleaning hard surfaces | |
| WO1999010458A1 (en) | Aqueous agents for cleaning hard surfaces | |
| DE19741911C1 (en) | Fatty acid polyglycol ester sulphate as foam booster for surfactants | |
| WO2019158411A1 (en) | Use of 1,2-alkanediols as lather boosters for citric acid ester surfactants comprising ethoxylated alcohols | |
| EP1171560A1 (en) | Cleaning agents for hard surfaces | |
| EP0866845A1 (en) | Syndet soaps | |
| WO1999010463A1 (en) | Aqueous agents for washing dishes by hand | |
| DE19806496C2 (en) | syndet soaps | |
| DE4407687A1 (en) | Aqueous hand dishwashing detergents | |
| DE19937294C2 (en) | Mouth and dentifrices and use of alkoxylated carboxylic acid esters | |
| EP1497406B1 (en) | Molded soap product containing one or several pregelatinized, cross-linked starch derivatives | |
| WO2002077140A1 (en) | Washing-up liquid for manual use |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| AK | Designated states |
Kind code of ref document: A2 Designated state(s): US |
|
| AL | Designated countries for regional patents |
Kind code of ref document: A2 Designated state(s): AT BE CH CY DE DK ES FI FR GB GR IE IT LU MC NL PT SE |
|
| 121 | Ep: the epo has been informed by wipo that ep was designated in this application | ||
| DFPE | Request for preliminary examination filed prior to expiration of 19th month from priority date (pct application filed before 20040101) | ||
| AK | Designated states |
Kind code of ref document: A3 Designated state(s): US |
|
| AL | Designated countries for regional patents |
Kind code of ref document: A3 Designated state(s): AT BE CH CY DE DK ES FI FR GB GR IE IT LU MC NL PT SE |
|
| 122 | Ep: pct application non-entry in european phase |