EP0445159A1

EP0445159A1 - Surface active mixtures

Info

Publication number: EP0445159A1
Application number: EP89912959A
Authority: EP
Inventors: Reinhard Müller; Klaus-Dieter Wisotzki; Karl Giede
Original assignee: Henkel AG and Co KGaA
Current assignee: Henkel AG and Co KGaA
Priority date: 1988-11-25
Filing date: 1989-11-16
Publication date: 1991-09-11
Also published as: EP0371339A3; ES2053920T3; WO1990006105A2; EP0371339B1; DE58903666D1; WO1990006105A3; EP0371339A2; ATE86095T1; DE3839769A1; CA2003517A1

Abstract

Aqueous surface active mixtures contain fatty alcohol ether sulphates and at least one other anionic tenside from the group of fatty alcohol ether tartrates and fatty alcohol ether citrates, containing between 0.01 and 3 wt.% of alkaline earth metal ions, referred to the total mixture. The fatty alcohol ether sulphates and the other above-mentioned anionic tensides are present in a weight ratio between 70:30 and 1:99. The mixtures are characterized by being well tolerated by the skin, by good detergency and good foaming.

Description

"Surface-active mixtures"

The invention relates to surface-active mixtures with low skin stress.

In order to enhance the cleaning action of aqueous preparations, these usually contain surface-active compounds. However, this increased cleaning effect is usually associated with increased skin stress. This is especially true for the important class of anionic surfactants.

Although this increased skin exposure is not problematic for normal uses, increased skin exposure should be avoided in the area of body cleansers. This applies in particular to people with sensitive or damaged skin, small children and babies. However, good skin tolerance is also important for products that are designed for frequent use, are used to clean the genital area or come into contact with mucous membranes.

There is therefore a need for body cleansing agents which, with sufficient cleaning performance and satisfactory other properties, are distinguished by a significantly lower skin load. It is known that by using magnesium ions in anionic surfactants such as fatty alcohol sulfates and ether sulfates, products with improved skin tolerance can be obtained.

European patent applications 199 131 and 209 910 relate to esters of hydroxycarboxylic acids such as citric acid and tartaric acid. By replacing part of the usual anionic surfactants with such esters, anionic surfactant solutions with improved skin tolerance are obtained.

It is also known that ampholytic and nonionic surfactants are often characterized by improved skin tolerance compared to anionic surfactants. However, these classes of surfactants cannot be used as a replacement for anionic surfactants for many areas of application, since they do not achieve their properties in crucial points, such as the cleaning action; The foam formation desired for shampoos by the consumer is generally not guaranteed if amphoteric surfactants are used exclusively or predominantly.

It can be seen from an article published in "Medical Cosmetology 13, 39-45 (1983)" that the skin tolerance of anion / amphoteric surfactant mixtures is in individual cases higher than that of the pure anionic surfactants. Thus, the skin tolerance of surfactant solutions can be increased by partially replacing the anionic surfactants with amphoteric surfactants, but disadvantages must be accepted with regard to important properties such as cleaning action and foaming. It was therefore the task to find cleaning agents which are distinguished both by a high cleaning performance and foaming, and by a significantly lower skin load.

It has now surprisingly been found that with certain combinations of anionic surfactants, which are comparatively little stressful to the skin within the class of anionic surfactants, a synergistic increase in skin tolerance occurs. On the basis of these surfactant combinations, it is possible to formulate cleaning agents that combine the advantages of anionic surfactants such as high cleaning performance and high foaming with increased skin tolerance.

The invention thus relates to surface-active aqueous mixtures comprising fatty alcohol ether sulfates and at least one further anionic surfactant from the group of fatty alcohol ether tartrates and fatty alcohol ether citrates, characterized in that (a) the

Mixtures contain 0.01-3% by weight of alkaline earth metal ions, based on the mixture as a whole, and (b) the fatty alcohol ether sulfates and the other anionic surfactants mentioned are present in a ratio of 70:30 to 1:99.

Fatty alcohol ether sulfates are to be understood as meaning the sulfates of the adducts of ethylene oxide (E0) and / or propylene oxide (PO) with saturated and / or unsaturated, linear and / or branched fatty alcohols, which are obtainable by known processes. The fatty alcohols on which the fatty alcohol ether sulfates are based can be pure compounds. However, it is usually preferred to use mixtures of various fatty alcohols obtained from native raw materials such as fats and oils. These fatty alcohols can be mixed with the alkylene oxides for example under pressure and in the presence of catalysts to fatty alcohol alkoxylates. It is known to the person skilled in the art that in alkoxylation reactions such as, for example, the addition of n mol of ethylene oxide to 1 mol of fatty alcohol by the known ethoxylation processes, it is not a uniform adduct, but rather a mixture of residual amounts of free fatty alcohol and a number of homologous (oligomeric) addition products of 1, 2, 3 , ... n, n + 1, n + 2 ... etc. Molecules of ethylene oxide per molecule of fatty alcohol is obtained. The average degree of ethoxylation (n) is defined by the starting quantities of fatty alcohol and ethylene oxide. The distribution curve of the homolog mixture usually has a maximum in the range between n-3 and n + 3. Further information on these points can be found, for example, in the magazine Soap / Cosmetics / Chemical Specialties, issue January 1988, p. 34. The desired fatty alcohol ether sulfates are finally obtained by reacting the fatty alcohol alkoxylates with, for example, sulfur trioxide and subsequent neutralization with alkali metal, alkaline earth metal or ammonium hydroxides.

It is preferred to use fatty alcohol ether sulfates whose linear or branched alkyl or alkenyl radicals contain 8-22 carbon atoms. It is also preferred to use fatty alcohol ether sulfates which have an average degree of alkoxylation of 2-15, in particular 3-10. The use of ethoxylated products is particularly preferred. In the context of the invention it is preferred to use fatty alcohol ether sulfates which already contain the amounts of alkaline earth metal ions required according to the invention as counterions.

Fatty alcohol ether tartrates to be used according to the invention are monoesters of tartaric acid with alcohols, the addition products of Represent ethylene oxide and / or propylene oxide on fatty alcohols. These fatty alcohols can be saturated and / or unsaturated, linear and / or branched. It is preferred to use fatty alcohols with 8-22 carbon atoms. Likewise preferred are degrees of alkoxylation of 2-15, in particular 3-10. With regard to the importance of the degree of alkoxylation, reference is made to the statements made in the description of the fatty alcohol ether sulfates. The mono-esterified tartaric acid can be used both directly and in the form of its salts, which are obtainable by reacting the non-esterified carboxyl group with appropriate bases. Preferred salts are the alkali metal, alkaline earth metal and ammonium salts. Manufacturing instructions for these compounds can be found in European patent application 209 910.

Fatty alcohol ether citrates to be used according to the invention are mono- and / or diesters of citric acid with alcohols, which are addition products of ethylene oxide and / or propylene oxide with fatty alcohols. These fatty alcohols can be saturated and / or unsaturated, linear and / or branched. It is preferred to use fatty alcohols with 8-22 carbon atoms. Likewise preferred are degrees of alkoxylation of 2-15, in particular 3-10. With regard to the importance of the degree of alkoxylation, reference is also made to the explanations in the description of the fatty alcohol ether sulfates. The mono- and / or diverestered citric acid can be used both directly and in the form of its salts, which are obtainable by reacting the non-esterified carboxyl group or groups with appropriate bases. Preferred salts are the alkali metal, alkaline earth metal and ammonium salts. Manufacturing instructions for these compounds can be found in European patent application 199 131. The ethoxylated compounds are preferred both with regard to the fatty alcohol ether tartrates and with regard to the fatty alcohol ether citrates.

A particularly good skin tolerance was found in mixtures which contain the fatty alcohol ether sulfates and the other anionic surfactants mentioned in a ratio of 60:40 to 10:90.

Mixtures containing a combination of fatty alcohol ether sulfates and fatty alcohol ether tartrates show particularly good properties. A very particularly preferred fatty alcohol ether tartrate is sodium lauryl (7 E0) tartrate.

Within the framework of the teaching according to the invention, such mixtures are preferred which contain 0.05-1% by weight, in particular 0.05-0.5% by weight, of alkaline earth metal ions. The magnesium ion is of particular importance.

The surface-active mixtures contain a total of 2-50% by weight of anionic surfactants. A content of 5-30% by weight is preferred.

In addition to the anionic surfactants, the surface-active mixtures according to the invention can additionally contain 0.5-20% by weight, in particular 1-10% by weight, of ampholytic and / or zwitterionic surfactants.

Ampholytic surfactants are surface-active compounds which, in addition to a C ₈ -C ₁₈ -alkyl or -acyl group, contain at least one free amino group and at least one -COOH or -S0 ₃ H group in the molecule and for formation inner salts are capable. Examples of suitable ampholytic surfactants are N-alkylglycine, N-alkylpropionic acid, N-alkylaminobutyric acid, N-alkyliminodipropionic acid, N-hydroxyethyl-N-alkylamidopropylglycine, N-alkyltaurine, N-alkyl sarcosine, 2-alkylaminopropionic acid and alkylaminoacetic acid each with about 8 to 18 C. Atoms in the alkyl group.

Zwitterionic surfactants are surface-active compounds that contain at least one quaternary ammonium group and at least one -COO (-) - or -SO ₃ (-) - group in the molecule. Particularly suitable zwitterionic surfactants are the so-called betaines such as the N-alkyl-N, N-dimethylammonium glycinate, for example the cocoalkyl-dimethylammonium glycinate, N-acyl-aminopropyl-N, N-dimethylammonium glycinate, for example the cocoacylaminopropyl-dimethylammonium glycinate, and 2-alkyl-3-carboxylmethyl-3-hydroxyethyl-imidazolines each having 8 to 18 carbon atoms in the alkyl or acyl group and the cocoacylaminoethyl-hydroxyethylcarboxymethylglycinate.

The skin-protecting properties of the agents according to the invention come into their own when they are formulated in such a way that they have a pH close to the neutral point. Agents with pH values in the range from 5.5 to 7.5, in particular from 6.5 to 7.5, are therefore preferred.

The agents according to the invention can be used in a large number of consumer products such as hair care products, hair shampoos, body care lotions, shower baths and products for infant care. In addition to the surfactant combination described, these products contain the usual ingredients such as emulsifiers, oil components, fats and waxes, solubilizers, thickeners, superfatting agents, biogenic agents, film formers, fragrances, dyes, pearlescent agents, foam stabilizers, preservatives and pH regulators.

As emulsifiers, the usual substances in cosmetic preparations such. B. fatty acid partial glycerides, fatty acid sorbitan partial esters and their ethoxylates, soaps, fatty alcohol sulfates, polyol fatty acid esters, fatty alcohol polyglycol ethers, lanolin, wool fatty alcohols and alkyl phosphates.

Usual oil components are substances such as paraffin oil, vegetable oils, fatty acid esters, squalane and 2-octyldodecanol, while the fats and waxes used are, for example, walnut, beeswax, montan wax, paraffin and cetylstearyl alcohol.

Low monohydric or polyhydric alcohols such as ethanol, isopropanol, ethylene glycol, propylene glycol, glycerol, 1,3-butylene glycol and diethylene glycol are usually used as solubilizers.

Substances such as polyethoxylated lanolin derivatives, lecithin derivatives and fatty acid alkanolamides can be used as superfatting agents, the latter also simultaneously serving as foam stabilizers.

Suitable thickeners are, for example, polysaccharides, in particular xanthan gum, guar gum, agar agar, alginates and tyloses, and also carboxymethyl cellulose and hydroxyethyl cellulose, further higher molecular weight polyethylene glycol mono- and diesters of fatty acids, polyacrylates, polyvinyl alcohol and polyvinyl pyrrolidone and finally electrolytes such as table salt and ammonium chloride, if desired in combination with alkyl ether sulfates.

Biogenic active ingredients are to be understood as plant extracts, protein breakdown products and vitamin complexes.

Common film formers are, for example, polyvinylpyrrolidone, vinylpyrrolidone-vinyl acetate copolymers, polymers of the acrylic acid series, quaternary cellulose derivatives and similar compounds.

The substances listed in the annex to the Cosmetics Ordinance are suitable as preservatives. As. Pearlescent agents are in particular glycol distearic acid esters such as ethylene glycol distearate, but also fatty acid monoglycol esters.

The dyes which can be used are the substances which are suitable and approved for cosmetic purposes, as compiled, for example, in the publication "Cosmetic Dyes" by the Dye Commission of the German Research Foundation, published by Verlag Chemie, Weinheim, 1984. These dyes are usually used in concentrations of 0.001 to 0.1% by weight, based on the mixture as a whole.

If desired, further components of the agents according to the invention are fragrances and substances which serve to adjust the pH of the agents. The mixtures according to the invention are preferably used in products which are used for washing, dyeing, waving or rinsing hair. The mixtures are particularly suitable for shampoos for washing hair.

The invention is explained in more detail by the following examples, without being restricted thereto.

B e i s p i e l e

1. Skin compatibility tests

The in vitro method developed by Zeidler and Reese was used to determine the skin compatibility of the surfactant mixtures, which is described in detail in the journal Ärzte Cosmetologie 13, 39-45 (1983).

The swelling of the pig epidermis served as a measure of the skin compatibility of the surfactant mixtures. The required epidermis was obtained immediately after young pigs were slaughtered and stored frozen.

For the measurement, punched-out epidermis strips measuring 1 cm × 6 cm were immersed for 30 minutes in the surfactant solutions, each containing 2% by weight of active substance, heated to 39 ° C. and adjusted to pH = 6.5. After a short rinse and removal of the adhering water, the weight of the swollen strips was determined by gently squeezing under defined conditions. The strips were then dewatered over calcium chloride for 24 hours and weighed again.

In order to eliminate influences that go back to specific properties of the respective animal or the place of removal (back, side), a standard measurement was carried out. A directly adjacent epidermis strip is treated in the same way with water instead of the surfactant solution.

The measured values t for the surfactant treatment and w for the treatment with water result from the relationship:

The standardized, relative swelling change Q is finally defined as

Q = * 100%

The Q value of the water-treated skin is therefore by definition 0%; negative values indicate anti-swelling properties.

The properties of mixtures of a surfactant mixture T it Eucarol (R) TA ^{1 were} examined. The surfactant mixture T was produced as follows:

A mixture of 96 kg of an adduct of 10 mol ethylene oxide with a coconut fatty alcohol C ₁₂ -C ₁₈ (54 weight percent C ₁₂ , 22 weight percent C ₁₄ , 10 weight percent C16, 12 weight percent C ₁₈ ), 113 kg of an adduct of 2 mol ethylene oxide with one Coconut fatty alcohol C ₁₂ -C ₁₄ (73 weight percent C ₁₂ , 27 weight percent C ₁₄ ) and 24.5 kg of an adduct of 2 moles of ethylene oxide with an oleyl-cetyl alcohol (65 weight percent C ₁₈ , 30 weight percent C ₁₆ , 5 weight percent C ₁₄ , Iodine number 50) was reacted with 74.4 kg of chlorosulfonic acid at a temperature of 10 to 20 ° C. in a continuous reactor to give the sulfuric acid half-ester and then neutralized with 55.5 kg of a 50% strength aqueous sodium hydroxide solution, diluted with 660 kg of water. The the alkyl ether sulfate obtained had an anionic surfactant content of 0.592 mol / kg (determined by two-phase titration according to DGF unit method H-III-10).

28.2 g of MgSO4.7 H ₂ O (0.114 mol), 4.6 g of trisodium citrate and 65 g of sodium chloride (1.1 mol) were added to 880 g of this ether sulfate. The surfactant mixture T thus obtained had an anionic surfactant content of approximately 0.59 mol / kg, corresponding to approximately 28 percent by weight (calculated with an average molecular weight of the anionic surfactants of 475).

The following Q values were measured for the mixtures of surfactant mixtures and Eucarol (R) TA ¹ :

Mixing ratio of the active substances

Surfactant mixture T: Eucarol TA O value

100: 0 36 ± 11

60: 40 16 ± 8.

40 60 2 ± 7

20: 80 - 8 ± 6

0: 100 36 ± 9

¹ aqueous solution of sodium laureth-7-tartrate, 25% active substance (ROL) 2. Determination of the foaming behavior

The foam behavior of the surfactant mixtures was determined using a motorized blow-foam apparatus in accordance with DIN 53902.

For the determination, 340 ml of surfactant solution (2% by weight of active substance in tap water from Düsseldorf-Holthausen at 18 ° dH) were prepared. The foam was generated at room temperature with a perforated plate (holes of 1 mm in diameter, 10 impacts at a frequency of 50 impacts / min, 13 cm stroke); it is very fine-pored and thus largely corresponds to a foam that forms on the head when shampooing. The measurements were carried out as a duplicate determination without grease contamination of the surfactant solution.

The foam behavior of a mixture known to be good foaming was compared

42 percent by weight Texapon (R) N 25 ² , (= 12% active substance)

10% by weight Dehyton (R) K ³ , (= 3% active substance)

1 percent by weight Comperlan (R) LS ⁴ (= 1% active ingredient) and 47 percent by weight water

certainly.

² Aqueous solution of sodium lauryl ether sulfate (approx. 28% active substance) (HENKEL)

³ Aqueous solution of a fatty acid amide derivative with betaine structure of the formula R-CONH- (CH ₂ ) 3-N ⁺ (CH ₃ ) 2-CH ₂ -COO- with the

CTFA name Cocoamidopropyl Betaine (approx. 30% active substance, approx. 5% NaCl, (HENKEL) ⁴ Mixture of coconut fatty acid diethanolamide (approx. 70%) and

Lauryl alcohol + 2 ethylene oxide (approx. 20%); Balance: water, free amine, free fatty acid, ester (HENKEL)

This mixture was diluted with water and also used in the form of a solution with 2% by weight of active substance. The following amounts of foam were measured: after 1 minute: 240 ml

after 3 minutes: 210 ml

after 5 minutes: 190 ml

The measured amounts of foam of the surfactant solutions according to the invention are given in the following table in percent based on the amount of foam of the comparison substance.

Mixing ratio

relative amounts of foam of the active substances

T surfactant mixture: Eucarol TA

after 1 min after 3 min after 5 mm 1 00: 0 87 95 95

60: 40 71 71 79

40. 60 88 90 95

20 80 83 81 84

0: 100 88 90 84

3. Skin compatibility of mixtures with ampholytic / zwitterionic surfactants Aqueous systems were investigated which contained 1.6% by weight of active substance of a mixture of surfactant mixture T and Eucarol TA (20:80, based on the active substances), 0.4% by weight of active substance of the ampholytic / zwitterionic surfactant A contained. The table also shows the value for a mixture which contains 2% by weight of active substance of the binary mixture of surfactant mixture T and Eucarol TA.

The following Q values were measured:

Surfactant A Q value - -8 ± 6

Dehyton (R) AB 30 ⁵ 11 ± 5

Dehyton (R) G ⁵ 17 ± 8

Dehyton (R) G-SF ⁷ 0 ± 7

Dehyton (R) -CB ⁸ 3 ± 7

⁵ Aqueous solution of a fatty amine derivative with a betaine structure,

CTFA name: Coco-betaine (approx. 30% active substance, approx. 6% NaCl) (HENKEL)

⁶ Aqueous solution of N-hydroxyethyl-N-cocoalkylamidoethyl glycinate sodium salt, CTFA name Cocoamphodiacetate, (approx. 30% active substance, approx. 7% NaCl) (HENKEL)

⁷ Aqueous solution of N-hydroxyethyl-N-alkylamidoethyl propionate, CTFA name Cocoamphodipropionate, (approx. 40% active substance) (HENKEL) ⁸ Aqueous solution of a fatty amine derivative with betaine structure, CTFA name: Coco-Betaine (approx. 31% active substance, approx.

6.5% NaCl) (HENKEL)

When examining analog systems with a mixture of surfactant mixture T and Eucarol TA (40:60, based on the active substances), the following Q values were measured:

Surfactant A Q value - 2 ± 7

Dehyton (R) AB 30 - 4 ± 5

Dehyton (R) G - 3 ± 4

Dehyton (R) G-SF 1 ± 7

Dehyton (R) CB 6 ± 4

Dehyton (R) K 8 ± 5

The foaming behavior of these ternary surfactant mixtures was determined in the same way as for the binary mixtures. The aqueous mixtures contained 1.6% by weight of active substance of the binary mixture of surfactant T / Eucarol TA in the ratio given below and 0.4% by weight of active substance of the third surfactant component A.

The measured amounts of foam of the surfactant solutions according to the invention are given in the following table in percent based on the amount of foam of the comparison substance. The table also shows the value for a mixture which contains 2% by weight of active substance of the binary mixture of surfactant mixture T and Eucarol TA. a) Binary mixture of surfactant T: Eucarol TA (40:60 based on active substance)

Surfactant component A relative amount of foam

after 1 min after 3 min after 5 min

b) binary mixture of surfactant T: Eucarol TA (20 80 based on active substance)

Surfactant component A relative amount of foam

after 1 min after 3 min after 5 min

4. Recipe examples a) Well foaming mild shampoo:

Component parts by weight

Eucarol (R) TA 28.8

Surfactant mixture T 17.1

Dehyton (R) G-SF 9.7

Edenor (R) KPK ⁹ 1.0

Comperlan (R) KD ¹⁰ 1.0

Cooking salt 2.0

Water ad 100

⁹ coconut palm kernel oil fatty acid + 9.2 ethylene oxide (HENKEL) 1 ⁰ coconut fatty acid diethanolamide (approx. 90 active substance) composition of the fatty acid: approx. 56% lauric acid approx. 21% myristic acid approx. 10% palmitic acid approx. 12% stearic and

Oleic acid b) Clear colorless shampoo:

Component parts by weight

Eucarol (R) TA 28.8

Surfactant mixture T 17.1

Dehyton (R) G-SF 9.7

Comperlan (R) KD 1.0 Amine oxide WS (R) 35 ¹¹ 1.0

Antil (R) 141 ¹² 1.0

Cooking salt 1.0

Water ad 100

¹¹ Aqueous solution of dimethyl cocoacylamidopropylamine oxide (approx.

35% active substance) (GOLDSCHMIDT)

¹² Aqueous solution of polyoxyethylene propylene glycol dioleate (approx.

40% active ingredient) GOLDSCHMIDT) c) finishing shampoo:

Component parts by weight

Eucarol (R) TA 28.8

Surfactant mixture T 17.1

Dehyton (R) G-SF 9.7

Edenor (R) KPK 1.0

Polymer JR (R) 40θl ³ 1.0

Cooking salt 1.0

Water ad 100

¹³ hydroxyethyl cellulose, quaternized (UNION-CARBIDE) d) colorless, clear, mild, well foaming shampoo with creamy foam

Component parts by weight

Eucarol (R) TA 28.8

T 18.2 surfactant mixture

Dehyton CB 9.7

Alkyl glucoside ¹⁴ 3.3

Edenor (R) KPK 1.0

Cooking salt 0.5

Glucamate DOE-120 ¹⁵ 0.5

Water ad 100

¹⁴ R ¹ O (Z) _x with Z = glucose, x = 1.4 and R ¹ = n-alkyl ( _C12-14 ),

60.8% active ingredient

¹⁵ poly (120) ethylene glycol methyl glucose dioleate (AMERCHOL)

e) clear, mild, well foaming conditioning shampoo

Component parts by weight

Eucarol (R) TA 28.8

T 18.2 surfactant mixture

Dehyton (R) G-SF 7.5

Alkylglucosidl ⁴ 3.3

Comperlan KD 1.0

Amine oxide WS (R) 35 1.0 Dehydol LS3 ¹⁶ 1.0

Cooking salt 1.0

Antil (R) 141 1.0

Merquat (R) 550 ¹⁷ 1.5

Ethanol 2.0

Water ad 100 ¹⁶ C _12-14 fatty alcohol + 3 ethylene oxide (HENKEL)

¹⁷ dimethyldiallylammonium chloride-acrylamide copolymer, 8% active ingredient in water (MERCK)

Claims

1. Surface-active aqueous mixtures containing fatty alcohol ether sulfates and at least one further anionic surfactant from the group of fatty alcohol ether tartrates and fatty alcohol ether citrates, characterized in that (a) the mixtures contain 0.01-3% by weight of alkaline earth metal ions, based on the mixture as a whole and (b) the fatty alcohol ether sulfates and said other anionic surfactants are present in a ratio of 70:30 to 1:99.

2. Mixtures according to claim 1, characterized in that they contain 0.05-1% by weight, in particular 0.05-0.5% by weight, of alkaline earth metal ions.

3. Mixtures according to one of claims 1 or 2, characterized in that they contain magnesium ions as alkaline earth metal ions.

4. Mixtures according to one of claims 1 to 3, characterized in that they contain anionic surfactants in amounts of 2-50% by weight, in particular 5-30% by weight, based on the mixture as a whole.

5. Mixtures according to one of claims 1 to 4, characterized in that they contain fatty alcohol ether sulfates, tartrates and / or citrates whose fatty alcohol alkoxylate groups independently of one another have a degree of alkoxylation of 2-15, in particular 3-10.

6. Mixtures according to one of claims 1 to 5, characterized

characterized in that they contain fatty alcohol ether sulfates and tartrates with an alkyl or alkenyl radical and / or fatty alcohol ether citrates with one or two alkyl or alkenyl radicals, which are independently linear or branched and contain 8-22 carbon atoms.

7. Mixtures according to one of claims 1 to 6, characterized in that they contain a combination of fatty alcohol ether sulfates and fatty alcohol ether tartrates.

8. Mixtures according to claim 7, characterized in that they contain sodium lauryl (7 EO) tartrate as the fatty alcohol ether tartrate.

9. Mixtures according to one of claims 1 to 8, characterized in that they additionally 0.5-20% by weight, in particular 1-10% by weight, of ampholytic and / or zwitterionic surfactants, in each case based on the whole mixture.

10. Mixtures according to one of claims 1 to 9, characterized in that they have a pH of 5.5-7.5, in particular 6.5-7.5.

11. Mixtures according to one of claims 1 to 10, characterized in that they are formulated as a shampoo.

12. Use of mixtures according to one of claims 1 to 11 for hair treatment.