PROCESS FOR THE PREPARATION OF N-HYDROXYPYRIDONE COMPOUNDS

Abstract

Disclosed herein is a process for the preparation of N-hydroxypyridone compounds of formula (I) from pyrone compounds,

Description

The invention relates to a process for the preparation of N-hydroxypyridone compounds from pyrone compounds, as well as the use of N-hydroxypyridone compounds as anti-dandruff agents or as preservatives.

Preservation of cosmetic formulations and household formulations extends their shelf life and therefore provides greater value for money for consumers. Furthermore, preservatives prevent consumers from distributing microbes around their home or on themselves and hence provide health benefits. Anti-microbial actives are well-described in the art and there are many available that provide excellent performance.

Piroctone Olamine, also known as Octopirox® (Clariant) and as piroctone ethanolamine, is a compound used in the treatment of fungal infections. The chemical name for Piroctone Olamine is the monoethanolamine salt of 1 hydroxy-4-methyl-6-(2,4,4-trimethylpentyl)-2(1H)-pyridone. Hence, Piroctone Olamine is the ethanolamine salt of the hydroxamic acid derivative piroctone.

Piroctone Olamine is often used in anti-dandruff shampoos as a safe alternative to the commonly used compound zinc pyrithione.

GB1440975, EP0158481, and WO2006/081969, among others, describe the use of Piroctone Olamine as an anti-dandruff agent and/or as a preservative.

Nevertheless, there is a desire for improved preservation and anti-fungal systems. In particular, there is a desire for reducing the concentration of such systems—but this requires improved efficacy to ensure that sufficient microbial growth (e.g. growth of bacteria, fungi or yeast) is inhibited. Consumers have generally become more conscious about the content of cosmetic and household products, and they desire reduced levels of ‘chemicals’, particularly those that may have a reputation for inhibiting the growth of microorganisms.

With the foregoing in mind, there remains a need for more efficacious preservation and anti-fungal substances, which meet present performance requirements as well as modern consumer desires and expectations.

WO2019/228988 discloses a process for forming 2-hydroxypyridine-1-oxide compounds such as piroctone from the corresponding amine salt such as piroctone olamine using an acid.

Surprisingly, it has now been found that N-hydroxypyridone compounds can be prepared directly from pyrone compounds and isolated in good yields.

The present invention relates to a process for the preparation of a compound of formula (I)

wherein

• • R¹ is H, linear or branched C1-C18-alkyl or C3-C8-cycloalkyl; and
  • R² is H, linear or branched C1-C18-alkyl or C3-C8-cycloalkyl;comprising the following steps:
  • a) reacting a compound of formula (II)

wherein

• • R¹ and R² are as in the compound of formula (I);
  • with hydroxylamine or a hydroxylammonium compound; and
  • b) crystallizing or precipitating the compound of formula (I) from an organic solvent.

An advantage of the compound of formula (I) such as piroctone is that there is a better activity to weight ratio than for the corresponding salt such as piroctone olamine, i.e. more efficacy per molecular weight of active. For example, the olamine counter ion in piroctone olamine accounts for approximately 20% of the overall mass of piroctone olamine but does not contribute to its anti-dandruff activity.

Using the process of the present invention, piroctone can be isolated in yields that are comparable to the yields obtained in a typical synthesis of piroctone olamine.

In a typical synthesis of piroctone olamine, the corresponding pyrone is reacted with hydroxylamine or a hydroxylammonium compound, and piroctone is isolated as its ethanolamine salt (piroctone olamine). So far, the intermediate piroctone could not be isolated in reasonable yields. Using the process of the present invention, piroctone can be prepared directly from the corresponding pyrone and isolated in good yields.

Advantageously, the process of the present invention provides direct access to N-hydroxypyridone compounds such as piroctone from pyrone compounds. Therefore, an additional step of converting a salt such as piroctone olamine into the free N-hydroxypyridone compound such as piroctone can be avoided, which saves time, costs, and resources. Accordingly, the process of the present invention is also interesting from an efficiency perspective as well as from a sustainability perspective.

The process of the invention is a process for the preparation of a compound of formula (I)

wherein

• • R¹ is H, linear or branched C1-C18-alkyl or C3-C8-cycloalkyl; and
  • R² is H, linear or branched C1-C18-alkyl or C3-C8-cycloalkyl.

Preferred are compounds of formula (I) wherein

• • R¹ is H, linear or branched C1-C12-alkyl or cyclohexyl; and
  • R² is H or linear or branched C1-C4-alkyl.

More preferred are compounds of formula (I) wherein

• • R¹ is H or linear or branched C6-C10-alkyl; and
  • R² is H or methyl.

Even more preferred are compounds of formula (I) wherein

• • R¹ is linear or branched C6-C10-alkyl; and
  • R² is methyl.

Particularly preferred is a compound of formula (I) wherein

• • R¹ is 2,4,4-trimethylpentyl; and
  • R² is methyl.

This compound is also referred to herein as piroctone.

Also preferred is a compound of formula (I) wherein

• • R¹ is H; and
  • R² is H.

Also preferred is a compound of formula (I) wherein

• • R¹ is cyclohexyl; and
  • R² is methyl.

The process of the invention comprises the following steps:

• • a) reacting a compound of formula (II)

wherein

• • R¹ and R² are as in the compound of formula (I);
  • with hydroxylamine or a hydroxylammonium compound; and
  • b) crystallizing or precipitating the compound of formula (I) from an organic solvent.

Step a)

In preferred compounds of formula (II) R¹ and R² are as in preferred compounds of formula (I). In more preferred compounds of formula (II) R¹ and R² are as in more preferred compounds of formula (I). In even more preferred compounds of formula (II) R¹ and R² are as in even more preferred compounds of formula (I). In particularly preferred compounds of formula (II) R¹ and R² are as in particularly preferred compounds of formula (I).

A compound of formula (II) is reacted with hydroxylamine or a hydroxylammonium compound. In one embodiment, a compound of formula (II) is reacted with hydroxylamine. Hydroxylamine can, for example, be used in the form of an aqueous solution. Hydroxylamine is, for example, commercially available as a 50% aqueous solution. In a preferred embodiment, a compound of formula (II) is reacted with a hydroxylammonium compound.

Hydroxylammonium compounds are particularly preferred. Suitable hydroxylammonium compounds are known to a person skilled in the art.

Preferred hydroxylammonium compounds are selected from hydroxylammonium sulfate, hydroxylammonium chloride, hydroxylammonium acetate, hydroxylammonium phosphate, hydroxylammonium nitrate, hydroxylammonium perchlorate, hydroxylammonium oxalate, hydroxylammonium hydrogen sulfate, hydroxylammonium 4-methylbenzenesulfonate and hydroxylammonium bromide.

More preferred hydroxylammonium compounds are selected from hydroxylammonium sulfate, hydroxylammonium chloride and hydroxylammonium acetate.

Even more preferred hydroxylammonium compounds are selected from hydroxylammonium sulfate and hydroxylammonium chloride.

A particularly preferred hydroxylammonium compound is hydroxylammonium sulfate.

Another particularly preferred hydroxylammonium compound is hydroxylammonium chloride.

Preferably, the molar ratio of the compound of formula (II) to hydroxylamine equivalents is from 1.0:1.0 to 1.0:4.0, more preferably from 1.0:1.8 to 1.0:3.0, even more preferably from 1.0:2.0 to 1.0:2.6, particularly preferably from 1.0:2.0 to 1.0:2.4, for example 1.0:2.2.

In a preferred embodiment, the molar ratio of the compound of formula (II) to the hydroxylammonium compound is from 1.0:0.5 to 1.0:2.0, more preferably from 1.0:0.9 to 1.0:1.5, even more preferably from 1.0:1.0 to 1.0:1.3, particularly preferably from 1.0:1.0 to 1.0:1.2, for example 1.0:1.1. Such molar ratios are preferred, for example, when hydroxylammonium sulfate is used as the hydroxylammonium compound.

In another preferred embodiment, the molar ratio of the compound of formula (II) to hydroxylamine or the hydroxylammonium compound is from 1.0:1.0 to 1.0:4.0, more preferably from 1.0:1.8 to 1.0:3.0, even more preferably from 1.0:2.0 to 1.0:2.6, particularly preferably from 1.0:2.0 to 1.0:2.4, for example 1.0:2.2. Such molar ratios are preferred, for example, when hydroxylammonium chloride or hydroxylammonium acetate is used as the hydroxylammonium compound.

In preferred embodiments, the compound of formula (II) is reacted with hydroxylamine or the hydroxylammonium compound in the presence of a base.

In one embodiment, the compound of formula (II) is reacted with hydroxylamine in the presence of a base. In another embodiment, the compound of formula (II) is reacted with hydroxylamine in the absence of a base.

In a preferred embodiment, the compound of formula (II) is reacted with the hydroxylammonium compound in the presence of a base.

Suitable bases are known to a person skilled in the art.

Examples of suitable bases are metal carbonates, metal hydrogen carbonates, or metal hydroxides, such as alkali metal carbonates, alkali metal hydrogen carbonates, alkali metal hydroxides, alkaline earth metal carbonates, alkaline earth metal hydrogen carbonates, or alkaline earth metal hydroxides.

Preferred bases are selected from alkali metal carbonates, alkali metal hydrogen carbonates, alkali metal hydroxides, and mixtures thereof.

More preferred bases are selected from alkali metal carbonates, alkali metal hydrogen carbonates, and mixtures thereof.

Even more preferred bases are selected from alkali metal carbonates.

Examples of suitable bases are lithium carbonate, sodium carbonate, potassium carbonate, cesium carbonate, lithium hydrogen carbonate, sodium hydrogen carbonate, potassium hydrogen carbonate, cesium hydrogen carbonate, lithium hydroxide, sodium hydroxide, potassium hydroxide, cesium hydroxide, calcium carbonate, magnesium carbonate, barium carbonate, nickel carbonate, zirconium carbonate, calcium hydroxide, magnesium hydroxide, barium hydroxide, nickel hydroxide, or zirconium hydroxide.

Preferred bases are selected from lithium carbonate, sodium carbonate, potassium carbonate, lithium hydrogen carbonate, sodium hydrogen carbonate, potassium hydrogen carbonate, sodium hydroxide, potassium hydroxide, and mixtures thereof.

More preferred bases are selected from lithium carbonate, sodium carbonate, potassium carbonate, lithium hydrogen carbonate, sodium hydrogen carbonate, potassium hydrogen carbonate, and mixtures thereof.

Even more preferred bases are selected from lithium carbonate, sodium carbonate, potassium carbonate, and mixtures thereof. Also even more preferred bases are selected from sodium carbonate, sodium hydrogen carbonate, and mixtures thereof.

A particularly preferred base is sodium carbonate.

Preferably, the molar ratio of hydroxylamine equivalents to base equivalents is from 1.0:0.5 to 1.0:3.0, more preferably from 1.0:0.8 to 1.0:2.0, even more preferably from 1.0:1.0 to 1.0:1.5, even more preferably from 1.0:1.0 to 1.0:1.2, particularly preferably from 1.0:1.0 to 1.0:1.1, for example 1.0:1.0.

In a preferred embodiment, the molar ratio of the hydroxylammonium compound to the base is from 1.0:0.5 to 1.0:3.0, more preferably from 1.0:0.8 to 1.0:2.0, even more preferably from 1.0:1.0 to 1.0:1.5, even more preferably from 1.0:1.0 to 1.0:1.2, particularly preferably from 1.0:1.0 to 1.0:1.1, for example 1.0:1.0. Such molar ratios are preferred, for example, when hydroxylammonium sulfate is used as the hydroxylammonium compound and an alkali metal carbonate (for example sodium carbonate) is used as the base.

In preferred embodiments, the compound of formula (II) is reacted with hydroxylamine or the hydroxylammonium compound in the presence of a solvent.

Suitable solvents are known to a person skilled in the art.

Preferred solvents are selected from organic solvents, water, and mixtures thereof.

Preferred organic solvents are selected from heptane, hexane, cyclohexane, methylcyclohexane, dimethylcyclohexane, toluene, benzene, methylene chloride, methanol, ethanol, isopropanol, tert-butanol, tert-amyl alcohol, dimethylformamide, dimethyl sulfoxide, tetrahydrofuran, acetonitrile, 2-aminopyridine, and mixtures thereof.

More preferred organic solvents are selected from heptane, hexane, cyclohexane, methylcyclohexane, toluene, 2-aminopyridine, and mixtures thereof.

A particularly preferred organic solvent is heptane.

In a preferred embodiment, the solvent is a mixture of an organic solvent and water.

In a more preferred embodiment, the solvent is a mixture of an organic solvent and water, wherein the organic solvent is selected from heptane, hexane, cyclohexane, methylcyclohexane, dimethylcyclohexane, toluene, benzene, methylene chloride, methanol, ethanol, isopropanol, tert-butanol, tert-amyl alcohol, dimethylformamide, dimethyl sulfoxide, tetrahydrofuran, acetonitrile, 2-aminopyridine, and mixtures thereof.

In an even more preferred embodiment, the solvent is a mixture of an organic solvent and water, wherein the organic solvent is selected from heptane, hexane, cyclohexane, methylcyclohexane, toluene, 2-aminopyridine, and mixtures thereof.

In a particularly preferred embodiment, the solvent is a mixture of an organic solvent and water, wherein the organic solvent is heptane.

Preferably, the solvent comprises at least 80 wt.-%, more preferably at least 90 wt.-%, even more preferably at least 95 wt.-%, particularly preferably at least 98 wt.-%, of an organic solvent, based on the total weight of the solvent.

In a preferred embodiment, the solvent comprises at least 80 wt.-%, more preferably at least 90 wt.-%, even more preferably at least 95 wt.-%, particularly preferably at least 98 wt.-%, of heptane, based on the total weight of the solvent.

Preferably, the compound of formula (II) is reacted with hydroxylamine or the hydroxylammonium compound at a temperature of 50 to 120° C., more preferably 60 to 100° C., even more preferably 70 to 90° C., particularly preferably 80 to 90° C.

Preferably, the compound of formula (II) is reacted with hydroxylamine or the hydroxylammonium compound for at least 4 hours, more preferably at least 8 hours, even more preferably at least 12 hours, particularly preferably at least 15 hours. For example, the compound of formula (II) is reacted with hydroxylamine or the hydroxylammonium compound for 8 to 24 hours, preferably 12 to 20 hours, particularly preferably 15 to 18 hours.

The reaction of the compound of formula (II) with hydroxylamine or the hydroxylammonium compound can be worked up in a usual manner, for example as described in Example 1.

Step b)

The compound of formula (I) is crystallized or precipitated from an organic solvent. In a preferred embodiment, the compound of formula (I) is crystallized from an organic solvent. In another embodiment, the compound of formula (I) is precipitated from an organic solvent.

Preferred organic solvents are selected from heptane, hexane, cyclohexane, methylcyclohexane, dimethylcyclohexane, and mixtures thereof.

A particularly preferred organic solvent is heptane.

Preferably, the compound of formula (I) is crystallized at a temperature of 0 to 25° C., more preferably 0 to 20° C., even more preferably 0 to 15° C., particularly preferably 0 to 10° C.

Preferably, the compound of formula (I) is crystallized from a solution of the compound of formula (I) in the organic solvent, wherein the organic solvent has a temperature of 50 to 75° C., preferably 55 to 70° C., particularly preferably 60 to 65° C. Preferably, the solution of the compound of formula (I) is cooled to a temperature of 0 to 25° C., more preferably 0 to 20° C., even more preferably 0 to 15° C., particularly preferably 0 to 10° C.

The crystallization of the compound of formula (I) can be carried out in a usual manner, for example as described in Example 1.

Preferably, the compound of formula (I) is precipitated at a temperature of 0 to 25° C., more preferably 0 to 20° C., even more preferably 0 to 15° C., particularly preferably 0 to 10° C.

Preferably, the compound of formula (I) is precipitated from a solution of the compound of formula (I) in the organic solvent, wherein the organic solvent has a temperature of 50 to 75° C., preferably 55 to 70° C., particularly preferably 60 to 65° C.

Preferably, the solution of the compound of formula (I) is cooled to a temperature of 0 to 25° C., more preferably 0 to 20° C., even more preferably 0 to 15° C., particularly preferably 0 to 10° C.

The precipitation of the compound of formula (I) can be carried out in a usual manner.

In a preferred embodiment, the same organic solvent is used in step a) and in step b). This is beneficial from a process perspective as well as from an economic and ecological perspective. In a particularly preferred embodiment, heptane is used as the organic solvent in step a) and in step b).

Further Aspects

The invention also relates to a compound of formula (I) obtained by the process of the present invention.

The invention also relates to the use of a compound of formula (I) obtained by the process of the present invention as an anti-dandruff agent or as a preservative.

The invention also relates to the use of a compound of formula (I)

wherein

• • R¹ is H, linear or branched C1-C18-alkyl or C3-C8-cycloalkyl; and
  • R² is H, linear or branched C1-C18-alkyl or C3-C8-cycloalkyl;as an anti-dandruff agent or as a preservative.

Preferred are compounds of formula (I) wherein

• • R¹ is H, linear or branched C1-C12-alkyl or cyclohexyl; and
  • R² is H or linear or branched C1-C4-alkyl.

More preferred are compounds of formula (I) wherein

• • R¹ is H or linear or branched C6-C10-alkyl; and
  • R² is H or methyl.

Even more preferred are compounds of formula (I) wherein

• • R¹ is linear or branched C6-C10-alkyl; and
  • R² is methyl.

Particularly preferred is a compound of formula (I) wherein

• • R¹ is 2,4,4-trimethylpentyl; and
  • R² is methyl.

Also preferred is a compound of formula (I) wherein

• • R¹ is H; and
  • R² is H.

Also preferred is a compound of formula (I) wherein

• • R¹ is cyclohexyl; and
  • R² is methyl.

In preferred embodiments, the invention relates to the use of a compound of formula (I) as an anti-dandruff agent.

In preferred embodiments, the invention relates to the use of a compound of formula (I) as a preservative.

Particularly preferably, the compound of formula (I) is incorporated into a cosmetic composition. Preferably, the cosmetic composition is a shampoo composition or hair conditioner composition. More preferably, the cosmetic composition is a shampoo composition, particularly preferably an anti-dandruff shampoo composition. Also more preferably, the cosmetic composition is a hair conditioner composition.

Preferably, the dandruff is caused by dandruff-causing organisms, more preferably Malassezia species, even more preferably Malassezia furfur and/or Malassezia globosa, particularly preferably Malassezia furfur, also particularly preferably Malassezia globosa.

The invention also relates to a cosmetic composition comprising a compound of formula (I), particularly preferably piroctone.

In preferred embodiments, the cosmetic composition of the invention comprises from 0.01 to 10 wt.-%, preferably from 0.05 to 5 wt.-%, more preferably from 0.1 to 2.0 wt.-%, even more preferably from 0.1 to 1.0 wt.-%, particularly preferably from 0.1 to 0.5 wt.-% of a compound of formula (I), particularly preferably piroctone, based on the total weight of the cosmetic composition.

For example, the cosmetic composition of the invention may be selected from the group consisting of shampoo, hair conditioner, hair tonic, cream rinse, body wash, bubble bath, bath oil, facial cleanser, cleansing mask, cleansing milk, micellar water, make-up remover, cleansing wipes, perfume, soaps, shaving soaps, shaving foams, cleansing foams, face mask, face cream, hand cream and body lotion.

Preferably, the cosmetic composition of the invention is a hair care composition, scalp care composition or skin care composition. More preferably, the cosmetic composition of the invention is a hair care or scalp care composition, particularly preferably a hair care and scalp care composition. Also more preferably, the cosmetic composition of the invention is a skin care composition.

Preferably, the cosmetic composition of the invention is a shampoo composition or hair conditioner composition. More preferably, the cosmetic composition of the invention is a shampoo composition, particularly preferably an anti-dandruff shampoo composition. Also more preferably, the cosmetic composition of the invention is a hair conditioner composition.

In preferred embodiments, the cosmetic composition of the invention is a shampoo composition. The shampoo composition can be in the form of rinse-off products or ‘dry shampoo’ products, can be opaque or transparent, and can be formulated in a wide variety of product forms, including creams, gels, emulsions, mousses and sprays. Preferably, the shampoo composition is in the form of a rinse-off product. The shampoo composition can, for example, be used on human hair and/or scalp or animal hair, preferably human hair and/or scalp.

In preferred embodiments, the cosmetic composition of the invention is a hair conditioner composition. The hair conditioner composition can be in the form of rinse-off products or leave-on products, can be opaque or transparent, and can be formulated in a wide variety of product forms, including creams, gels, emulsions, mousses and sprays. Preferably, the hair conditioner composition is in the form of a rinse-off product.

In at least one embodiment, the cosmetic composition is in liquid form. In an alternative embodiment, the cosmetic composition is in solid form. Optionally, the cosmetic composition is in powdered or granulated form. This is advantageous in that it is not needed to ship liquid, which is typically heavy, over long distances, which has economic and environmental benefits. A solid form can be achieved by spray drying the composition or by using a rotary evaporator. A solid form can also be achieved by extrusion or pressing. The composition can be converted into liquid form after it has been shipped, e.g. by adding water.

The invention is further illustrated by the following examples, without being limited thereby.

EXAMPLES

As used herein, the term “Piroctone” or “piroctone” refers to a compound of formula (I) wherein R¹ is 2,4,4-trimethylpentyl; and R² is methyl.

As used herein, the term “Pyron” refers to a compound of formula (II) wherein R¹ is 2,4,4-trimethylpentyl; and R² is methyl.

Example 1

Typical procedure for the synthesis of Piroctone from Pyron in heptane:

In a 4-neck 1 L round bottom flask equipped with a mechanical stirrer, a reflux condenser and an internal thermometer the following reagents are placed: Pyron (150.00 g), sodium carbonate (80.03 g) and hydroxylammonium sulfate (123.48 g). Under stirring, heptane (technical, 99 g) is added to the mixture followed by water (1.71 g). The mixture is then heated to its boiling point. Gas evolution starts at an internal temperature of 74° C. and finishes by 86° C. The mixture is kept at this temperature under stirring for 16 h. After this time, the temperature of the mixture is reduced to 60-65° C. and warm water is added (60° C., 355 g) after which the stirring is continued for 30 minutes. The biphasic mixture is then transferred to a heated separatory funnel kept at a temperature of at least 65° C. The aqueous layer is separated (typically having a pH of 8) and a mixture of sulfuric acid and water (6 g H₂SO₄ dissolved in 12 g H₂O) is used to extract the organic layer yielding an aqueous layer (pH 5 to 6) which is separated. Finally, water (25 mL) is used to wash the organic layer, the aqueous layer is separated. The organic phase is transferred to a 1 L round bottom flask using heptane (30 g) to rinse the separatory funnel. The mixture is concentrated in a rotary evaporator to remove water azeotropically (60-65° C.). Mass after concentration: ˜185 g. Heptane (30 mL) is added quickly after concentration and the mixture is left to cool down to room temperature under constant stirring. During this process crystals start to form in the mixture, which however do not interfere with the stirring. The mixture is cooled to 6° C. by placing it in an ice bath and filtered over a G3 sintered glass filter. The filter cake is washed 3 times with heptane (total 130 g). The obtained solid is further dried on a vacuum line (oil pump) overnight yielding 84.47 g of Piroctone. The mother liquor of the filtration is concentrated to dryness on the rotary evaporator. The residue is redissolved in heptane (50 mL) and left to recrystallize in a fridge (4° C.). After filtration and drying, additional 3.55 g of Piroctone are obtained. The new mother liquor is discarded.

Yield (Piroctone): 88.02 g Piroctone, corresponding to a yield of 57.9%

Remark:

Crystallization or precipitation of piroctone gives comparable yields irrespective of whether heptane is added or not after the water has been removed azeotropically.

Example 2 PP7T

Cosmetic compositions (ingredients are given in wt %)

Example	2a	2b	2c	2d	2e
Composition	Liquid	Body	Wet wipe	Sham-	Sham-
	soap	wash	lotion	poo	poo
Piroctone	0.5	0.5	0.5	0.5	0.5
SLES	10	—	—	—	9
Cocamido-	2	4.5	—	—	2
propylbetaine
Cocamide MEA	—	—	—	—	1
Sodium Cocoyl	—	2	1	2	—
Glutamate
Sodium Cocoyl	—	2	1	2	—
Glycinate
Sodium Cocoyl	—	2	—	—	—
Isethionate
Cocoyl Methyl	—	3	2	—	—
Glucamide
EGDS	—	0.5	—	—	0.7
PEG-7 Glyceryl	—	—	1	—	—
Cocoate
Cocoyl Glucoside	—	—	—	5	—
Lauryl Glucoside	—	—	—	5	—
Acrylates Copolymer	—	—	—	2	—
Glycerin	—	—	—	1	2
Panthenol	—	—	—	0.2	0.2
Dimethicone	—	—	—	—	—
Polyquaternium 7 (PQ-7)	—	—	—	—	0.6
Guar Hydroxypropyl-	—	—	—	—	0.3
trimonium Chloride
Hydrolyzed Protein	—	—	—	—	0.1
N-fatty acyl-N-methyl	1.5	2	1.0	1.5	2
cyclic glucamide
NaCl	1.5	1.0	0.5	0.3	1.5
Water	QSP	QSP	QSP	QSP	QSP
Total	100	100	100	100	100

Example 3

Cosmetic compositions (ingredients are given in wt %)

Example	3a	3b	3c	3d
Composition	Body	Intensive	Anti-	Baby
	Lotion	hand and	ageing	cream
		body	night
		lotion	cream
Piroctone	0.2	0.2	0.2	0.1
Ethyhexyl Stearate	7	—	—	—
Decyl Oleate	5	—	—	—
Plantasens ® Natural	3	—	—	—
Emulsifier HE 20 (Clariant),
which is Cetearyl
Glucoside (and) Sorbitan
Olivate
Dimethicone	2	—	—	—
Glycerin	3	3	7	—
Xanthan Gum	0.2	—	—	—
Aristoflex ® AVC from	0.5	1	—	—
Clariant (Ammonium
Acryloyldimethyltaurate/
VP Copolymer)
Polyglyceryl-2-	—	0.5	—	2
Sesquiisostearate
Trilaureth-4 Phosphate	—	2	—	—
Mineral Oil	—	5	—	—
(Paraffinum Liquidum)
Plantasens ® Refined	—	2	—	—
Organic Babassu Butter
from Clariant (Orbignya
Oleifera Seed Oil)
Squalane	—	2	12	—
Macadamia Ternifolia	—	2	—	—
Seed Oil (and) Crambe
Abyssinica Seed Oil (and)
Orbignya Oleifera Seed
Oil
Silcare ® Silicone SEA	—	0.5	—	—
from Clariant (Trideceth-
9 PG-Amodimethicone
and Trideceth-12)
Cetearyl Alcohol	—	2	—	—
Isopropyl Palmitate	—	4	—	—
Dow Corning® 345	—	—	10	—
(Cyclopentasiloxane and
Cyclohexasiloxane)
Paraffin Oil, low viscosity	—	—	4	10
Petrolatum	—	—	4	15
Cetyl Alcohol	—	—	3	—
Cutina ® GMS	—	—	2.5	—
(Glyceryl Stearate)
PEG-40 Stearate	—	—	3	—
Cera Alba Wax	—	—	2	—
Mangifera Indica	—	—	2	—
(Mango) Seed Butter
Abyssinian Oil (and)	—	—	0.5	—
Phytosterols (and) Olea
Europea (Olive) Oil
Unsaponifiables
Sorbitan Tristearate	—	—	0.3	—
Ubiquinone	—	—	0.05	—
Aristoflex ® Velvet from	—	—	0.3	—
Clariant (Polyacrylate
Crosspolymer-11)
Hostacerin ® SFO from	—	—	—	3.5
Clariant (Sunflower Seed
Oil Sorbitol Esters)
Paracera ® M (Cera	—	—	—	2
Microcristallina)
Beeswax	—	—	—	1
Magnesium Stearate	—	—	—	1
Talc	—	—	—	10
Zinc oxide	—	—	—	10
Allantoin (Clariant)	—	—	—	0.3
Extrapon Hamamelis	—	—	—	2
D-Panthenol	—	—	—	2
N-fatty acyl-N-methyl cyclic	1.5	2	1.0	1.5
glucamide
Water	QSP	QSP	QSP	QSP
Total	100	100	100	100

Example 4

Cosmetic compositions (ingredients are given in wt %)

Example	4a	4b	4c	4d	4e	4f
Composition	Soap	Soap	Body	Sham-	Wash	Body
	formu-	bar	wash	poo	cream	wash
	lation
Piroctone	0.5	1.0	0.5	0.5	0.5	0.5
Sodium Lauryl	—	—	10	—	—	—
Sulfate
Ammonium Lauryl	—	—	—	12	—	—
Sulfate
Sodium Lauryl Ether	15	—	2	—	—	—
Sulfate (SLES)
Cocamido-	7	—	2	3	—	2
propylbetaine
Cocamide MEA	—	—	1	—	—	2
Lauric Acid	0.5	2	—	—	—	10
Myristic Acid	1.5	2	—	—	—	10
Stearic Acid	0.5	2	—	—	10	—
Palmitic Acid	—	2	—	—	—	10
Potassium	—	2	—	—	—	—
Tallowate
Sodium Palm	—	20	—	—	—	—
Kernelate
Sodium Cocoate	—	60	—	—	—	—
Lauryl Glucoside	—	—	—	4	—	—
Sodium Cocoyl	—	—	—	—	14	—
Isethionate
Glycerin	—	5	—	—	—	5
Cetearyl Alcohol	1.5	—	—	—	2	—
Dimethicone	—	—	—	—	0.1	—
Polyquaternium 7	—	—	—	0.2	—	—
(PQ-7)
Guar	—	—	0.3	—	—	—
Hydroxypropyl-
trimonium
Chloride
Hydrolyzed Protein	—	—	—	0.1	—	—
N-fatty acyl-N-methyl	1.5	2	1.0	1.5	1	0.8
cyclic glucamide
NaCl	1.5	—	0.5	0.3	—	2.5
Water	QSP	QSP	QSP	QSP	QSP	QSP
Total	100	100	100	100	100	100

Example 5

Hair Conditioner Compositions

Example	5a	5b	5c	5d	5e	5f
Ingredient	wt.-	wt.-	wt.-	wt.-	wt.-	wt.-
	%	%	%	%	%	%
Piroctone	0.4	0.5	0.3	0.4	0.5	0.6
Cetearyl Alcohol	4.0	4.0	4.0	4.0	4.0	4.0
CTAC	2.0	—	—	1.0	1.0	—
BTAC	—	2.0	—	1.0	—	1.0
BTMS	—	—	2.0	—	1.0	1.0
Xiameter PMX-200	0.2	0.2	0.2	0.2	0.2	0.2
(dimethicone)
Water	Ad.	Ad.	Ad.	Ad.	Ad.	Ad.
	100	100	100	100	100	100

Example 6

Hair Conditioner Compositions

Example	6a	6b	6c	6d	6e	6f
Ingredient	wt.-	wt.-	wt.-	wt.-	wt.-	wt.-
	%	%	%	%	%	%
Piroctone	0.4	0.5	0.3	0.4	0.5	0.6
Cetearyl Alcohol	4.0	4.0	4.0	4.0	4.0	4.0
CTAC	0.5	0.5	0.5	—	—	—
BTAC	—	—	—	0.5	0.5	0.5
Genadvance ® Life	1.5	—	—	1.5	—	—
Genadvance ® Repair	—	1.5	—	—	1.5	—
Genadvance ® Hydra	—	—	1.5	—	—	1.5
Xiameter PMX-200	0.2	0.2	0.2	0.2	0.2	0.2
(dimethicone)
Water	Ad.	Ad.	Ad.	Ad.	Ad.	Ad.
	100	100	100	100	100	100
Genadvance ® Life: Clariant, INCI = Polyquaternium-116 und Butylene Glycol
Genadvance ® Repair: Clariant, INCI = Quaternium-98
Genadvance ® Hydra: Clariant, INCI = Lauryl/Myristyl Polyricinoleate & Glycerin

Example 7

Hair conditioner compositions

Example	7a	7b	7c	7d	7e	7f
Ingredient	wt.-	wt.-	wt.-	wt.-	wt.-	wt.-
	%	%	%	%	%	%
Piroctone	0.4	0.5	0.3	0.4	0.5	0.6
Cetearyl Alcohol	4.0	4.0	4.0	4.0	4.0	4.0
CTAC	0.2	0.2	0.2	—	—	—
BTAC	—	—	—	0.2	0.2	0.2
Genadvance ® Life	1.8	—	—	1.8	—	—
Genadvance ® Repair	—	1.8	—	—	1.8	—
Genadvance ® Hydra	—	—	1.8	—	—	1.8
Xiameter PMX-200	0.2	0.2	0.2	0.2	0.2	0.2
(dimethicone)
Water	Ad.	Ad.	Ad.	Ad.	Ad.	Ad.
	100	100	100	100	100	100
Genadvance ® Life: Clariant, INCI = Polyquaternium-116 und Butylene Glycol
Genadvance ® Repair: Clariant, INCI = Quaternium-98
Genadvance ® Hydra: Clariant, INCI = Lauryl/Myristyl Polyricinoleate & Glycerin

Example	8a	8b	8c	8d
Ingredient	wt %	wt %	wt %	wt %
Aqua	To 100	To 100	To 100	To 100
Piroctone	0.1	0.3	0.7	1.0
sodium laureth sulfate	8	8	8	8
sodium lauryl sulfate	8	8	8	8
cocamide MIPA	4	4	4	4
glycerin	3.5	3.5	3.5	3.5
glycol distearate	3	3	3	3
sodium chloride	2.5	2.5	2.5	2.5
dimethicone	2	2	2	2
PPG-5-ceteth-20	1.5	1.5	1.5	1.5
Hair conditioning agent	1	1	1	1
carbomer	0.4	0.4	0.4	0.4
niacinamide	0.2	0.2	0.2	0.2
pyridoxine HCl	0.2	0.2	0.2	0.2
guar hydroxypropyltrimonium	0.2	0.2	0.2	0.2
chloride
hydrolyzed soy protein	0.2	0.2	0.2	0.2
methyl cocoate	0.15	0.15	0.15	0.15
sodium cocoate	0.15	0.15	0.15	0.15
citric acid	As needed, pH 4.5-6.5
sodium hydroxide	As needed, pH 4.5-6.5
Colorant	As needed

Example 9

Shampoo Compositions

Example	9a	9b	9c	9d
Ingredient	wt %	wt %	wt %	wt %
Aqua	To 100	To 100	To 100	To 100
Piroctone	0.1	0.3	0.7	1.0
sodium laureth sulfate	14	14	14	14
coco-betaine	4	4	4	4
glycerin	3	3	3	3
glycol distearate	2.5	2.5	2.5	2.5
dimethicone	2	2	2	2
Hair conditioning agent	1.5	1.5	1.5	1.5
niacinamide	0.5	0.5	0.5	0.5
coconut oil	0.5	0.5	0.5	0.5
sodium chloride	0.5	0.5	0.5	0.5
olive fruit oil	0.4	0.4	0.4	0.4
PPG-5-ceteth-20	0.3	0.3	0.3	0.3
trideceth-6	0.25	0.25	0.25	0.25
polyquaternium-6	0.25	0.25	0.25	0.25
amodimethicone	0.2	0.2	0.2	0.2
carbomer	0.2	0.2	0.2	0.2
cetrimonium chloride	0.15	0.15	0.15	0.15
citric acid	As needed, pH 4.5-6.5
sodium hydroxide	As needed, pH 4.5-6.5
Colorant	As needed

Example 10

Shampoo Compositions

Example	10a	10b	10c	10d
Ingredient	wt %	wt %	wt %	wt %
Aqua	To 100	To 100	To 100	To 100
Piroctone	0.1	0.3	0.7	1.0
ammonium lauryl sulfate	16	16	16	16
cocoamidopropyl betaine	5	5	5	5
sodium chloride	2.5	2.5	2.5	2.5
niacinamide	2	2	2	2
Hair conditioning agent	1	1	1	1
hydroxypropyl guar	0.8	0.8	0.8	0.8
hydroxypropyltrimonium chloride
propylene glycol	0.1	0.1	0.1	0.1
citric acid	As needed, pH 4.5-6.5
sodium hydroxide	As needed, pH 4.5-6.5
Colorant	As needed

Example 11

Shampoo Compositions

Example	11a	11b	11c	11d
Ingredient	wt %	wt %	wt %	wt %
Aqua	To 100	To 100	To 100	To 100
Piroctone	0.1	0.3	0.7	1.0
sodium laureth sulfate	16	16	16	16
glycol distearate	4	4	4	4
coco-betaine	2.5	2.5	2.5	2.5
glycerin	2	2	2	2
sodium chloride	1.5	1.5	1.5	1.5
dimethicone	1.5	1.5	1.5	1.5
Hair conditioning agent	1.5	1.5	1.5	1.5
niacinamide	1	1	1	1
guar hydroxypropyltrimonium	0.8	0.8	0.8	0.8
chloride
cocamide MIPA	0.5	0.5	0.5	0.5
PPG-5-ceteth-20	0.2	0.2	0.2	0.2
fumaric acid	0.15	0.15	0.15	0.15
carbomer	0.15	0.15	0.15	0.15
pyridoxine HCl	0.1	0.1	0.1	0.1
citric acid	As needed, pH 4.5-6.5
sodium hydroxide	As needed, pH 4.5-6.5
Colorant	As needed

Example 12

Shampoo Compositions

Example	12a	12b	12c	12d
Ingredient	wt %	wt %	wt %	wt %
Aqua	To 100	To 100	To 100	To 100
Piroctone	0.1	0.3	0.7	1.0
sodium laureth sulfate	16	16	16	16
coco-betaine	4	4	4	4
niacinamide	2	2	2	2
Ribes nigrum oil	1.5	1.5	1.5	1.5
cocamide MIPA	1.5	1.5	1.5	1.5
sodium chloride	1.5	1.5	1.5	1.5
Hair conditioning agent	1.2	1.2	1.2	1.2
sodium cocoate	0.8	0.8	0.8	0.8
cocamide MIPA	0.5	0.5	0.5	0.5
Olea europaea oil (olive) fruit oil	0.3	0.3	0.3	0.3
PEG-55 propylene glycol oleate	0.3	0.3	0.3	0.3
PEG-60 hydrogenated castor oil	0.3	0.3	0.3	0.3
polyquaternium-7	0.2	0.2	0.2	0.2
amodimethicone	0.15	0.15	0.15	0.15
propylene glycol	0.1	0.1	0.1	0.1
Butyrospermum parkii butter	0.1	0.1	0.1	0.1
laureth-5 carboxylic acid	0.1	0.1	0.1	0.1
citric acid	As needed, pH 4.5-6.5
sodium hydroxide	As needed, pH 4.5-6.5
Colorant	As needed

Example 13

Shampoo Compositions

Example	13a	13b	13c	13d
Ingredient	wt %	wt %	wt %	wt %
Aqua	To 100	To 100	To 100	To 100
Piroctone	0.1	0.3	0.7	1.0
sodium laureth sulfate	10	10	10	10
disodium cocamphodiacetate	5	5	5	5
glycerin	3	3	3	3
glycol distearate	2	2	2	2
sodium chloride	1.5	1.5	1.5	1.5
Hair conditioning agent	1.5	1.5	1.5	1.5
cocamide MEA	1	1	1	1
polyquaternium-10	1	1	1	1
carbomer	0.3	0.3	0.3	0.3
citric acid	As needed, pH 4.5-6.5
sodium hydroxide	As needed, pH 4.5-6.5
Colorant	As needed

Example 14

Shampoo Compositions

Example	14a	14b	14c	14d
Ingredient	wt %	wt %	wt %	wt %
Aqua	To 100	To 100	To 100	To 100
Piroctone	0.1	0.3	0.7	1.0
sodium laureth sulfate	12	12	12	12
coco-betaine	3	3	3	3
cocamide MIPA	2	2	2	2
sodium chloride	1.8	1.8	1.8	1.8
Olea europaea (olive) fruit oil	0.5	0.5	0.5	0.5
Hair conditioning agent	0.5	0.5	0.5	0.5
PPG-5-ceteth-20	0.4	0.4	0.4	0.4
PEG-55 propylene glycol oleate	0.4	0.4	0.4	0.4
PEG-60 hydrogenated castor oil	0.25	0.25	0.25	0.25
polyquaternium-10	0.25	0.25	0.25	0.25
amodimethicone	0.15	0.15	0.15	0.15
propylene glycol	0.15	0.15	0.15	0.15
laureth-5	0.1	0.1	0.1	0.1
citric acid	As needed, pH 4.5-6.5
sodium hydroxide	As needed, pH 4.5-6.5
Colorant	As needed

Example 15

Shampoo Compositions

Example	15a	15b	15c	15d
Ingredient	wt %	wt %	wt %	wt %
Aqua	To 100	To 100	To 100	To 100
Piroctone	0.1	0.3	0.7	1.0
ammonium lauryl sulfate	15	15	15	15
cocamidopropyl betaine	3	3	3	3
sodium chloride	2	2	2	2
propylene glycol	1.8	1.8	1.8	1.8
hydroxypropyl guar	1.5	1.5	1.5	1.5
hydroxypropyltrimonium chloride
Hair conditioning agent	1	1	1	1
citric acid	As needed, pH 4.5-6.5
sodium hydroxide	As needed, pH 4.5-6.5
Colorant	As needed

Example 16

Shampoo Compositions

Example	16a	16b	16c	16d
Ingredient	wt %	wt %	wt %	wt %
Aqua	To 100	To 100	To 100	To 100
Piroctone	0.1	0.3	0.7	1.0
sodium cocoyl isethionate	4	4	4	4
sodium lauryl sulfoacetate	3	3	3	3
disodium laureth sulfosuccinate	2.5	2.5	2.5	2.5
cocamidopropyl betaine	2.5	2.5	2.5	2.5
sodium lauroyl sarcosinate	2.5	2.5	2.5	2.5
glycol distearate	2	2	2	2
glycereth-26	1.8	1.8	1.8	1.8
decyl glucoside	1.5	1.5	1.5	1.5
hydrogenated coconut acid	1.4	1.4	1.4	1.4
PPG-5-ceteth-20	1.3	1.3	1.3	1.3
divinyldimethicone/dimethicone	1.2	1.2	1.2	1.2
copolymer
sodium chloride	1.1	1.1	1.1	1.1
amodimethicone	1	1	1	1
Hair conditioning agent	1	1	1	1
polyquaternium-7	1	1	1	1
polyquaternium-10	0.7	0.7	0.7	0.7
sodium isethionate	0.5	0.5	0.5	0.5
PEG-55 propylene glycol oleate	0.4	0.4	0.4	0.4
propylene glycol	0.4	0.4	0.4	0.4
carbomer	0.4	0.4	0.4	0.4
C11-15 pareth-7	0.3	0.3	0.3	0.3
glycerin	0.3	0.3	0.3	0.3
trideceth-12	0.25	0.25	0.25	0.25
laureth-9	0.2	0.2	0.2	0.2
hydroxypropyltrimonium	0.1	0.1	0.1	0.1
hydrolyzed wheat protein
citric acid	As needed, pH 4.5-6.5
sodium hydroxide	As needed, pH 4.5-6.5
Colorant	As needed

Example 17

Shampoo Compositions

Example	17a	17b	17c	17d
Ingredient	wt %	wt %	wt %	wt %
Aqua	To 100	To 100	To 100	To 100
Piroctone	0.1	0.3	0.7	1.0
sodium methyl cocoyl taurate	5	5	5	5
laureth-5 carboxylic acid	4	4	4	4
sodium chloride	2	2	2	2
cocamidopropyl betaine	2	2	2	2
glycerin	1.8	1.8	1.8	1.8
glycol distearate	1.5	1.5	1.5	1.5
Hair conditioning agent	1.5	1.5	1.5	1.5
polyquaternium-10	1	1	1	1
PPG-5 ceteth-20	0.5	0.5	0.5	0.5
sodium lauroyl glutamate	0.4	0.4	0.4	0.4
propylene glycol	0.2	0.2	0.2	0.2
PEG-55 propylene glycol oleate	0.15	0.15	0.15	0.15
Argania spinosa kernel oil	0.1	0.1	0.1	0.1
citric acid, lactic acid	As needed, pH 4.5-6.5
sodium hydroxide	As needed, pH 4.5-6.5
Colorant	As needed

Example 18

Shampoo Compositions

Example	18a	18b	18c	18d
Ingredient	wt %	wt %	wt %	wt %
Aqua	To 100	To 100	To 100	To 100
Piroctone	0.1	0.3	0.7	1.0
sodium laureth sulfate	10	10	10	10
disodium cocoamphodiacetate	4	4	4	4
glycol distearate	2	2	2	2
sodium chloride	1.5	1.5	1.5	1.5
Hair conditioning agent	1.3	1.3	1.3	1.3
carbomer	0.4	0.4	0.4	0.4
diaminopyrimidine oxide	0.3	0.3	0.3	0.3
disodium ricinoleamido MEA	0.3	0.3	0.3	0.3
sulfosuccinate
propylene glycol	0.2	0.2	0.2	0.2
panthenol	0.1	0.1	0.1	0.1
polyquaternium-10	0.1	0.1	0.1	0.1
citric acid	As needed, pH 4.5-6.5
sodium hydroxide,	As needed, pH 4.5-6.5
ammonium hydroxide
Colorant	As needed

Example 19

Shampoo Compositions

Example	19a	19b	19c	19d
Ingredient	wt %	wt %	wt %	wt %
Aqua	To 100	To 100	To 100	To 100
Piroctone	0.1	0.3	0.7	1.0
sodium cocoyl isethionate	4.5	4.5	4.5	4.5
sodium lauryl sulfoacetate	3	3	3	3
disodium laureth sulfosuccinate	2.5	2.5	2.5	2.5
cocamidopropyl betaine	2.5	2.5	2.5	2.5
sodium lauroyl sarcosinate	2.3	2.3	2.3	2.3
glycol distearate	2	2	2	2
glycereth-26	1.8	1.8	1.8	1.8
decyl glucoside	1.7	1.7	1.7	1.7
hydrogenated coconut acid	1.5	1.5	1.5	1.5
PPG-5-ceteth-20	1.5	1.5	1.5	1.5
PEG-55 propylene glycol oleate	1.5	1.5	1.5	1.5
propylene glycol	1.5	1.5	1.5	1.5
sodium chloride	1.5	1.5	1.5	1.5
divinyldimethicone/dimethicone	1	1	1	1
copolymer
polyquaternium-7	1	1	1	1
amodimethicone	1	1	1	1
Hair conditioning agent	1	1	1	1
polyquaternium-10	0.8	0.8	0.8	0.8
sodium isethionate	0.6	0.6	0.6	0.6
carbomer	0.6	0.6	0.6	0.6
C11-15 pareth-7	0.4	0.4	0.4	0.4
glycerin	0.3	0.3	0.3	0.3
laureth-9	0.2	0.2	0.2	0.2
citric acid	As needed, pH 4.5-6.5
sodium hydroxide	As needed, pH 4.5-6.5
Colorant	As needed

Example 20

Shampoo Compositions

Example	20a	20b	20c	20d
Ingredient	wt %	wt %	wt %	wt %
Aqua	To 100	To 100	To 100	To 100
Piroctone	0.1	0.3	0.7	1.0
cocamidopropyl betaine	5	5	5	5
sodium lauryl sulfoacetate	4	4	4	4
disodium laureth sulfosuccinate	3.5	3.5	3.5	3.5
sodium lauroyl sarcosinate	3	3	3	3
glycol distearate	2	2	2	2
sodium chloride	1.7	1.7	1.7	1.7
decyl glucoside	1.5	1.5	1.5	1.5
Hair conditioning agent	1.5	1.5	1.5	1.5
polyquaternium-10	1	1	1	1
PPG-5-ceteth-20	1	1	1	1
coco-betaine	0.8	0.8	0.8	0.8
PEG-55 propylene glycol	0.8	0.8	0.8	0.8
oleate
propylene glycol	0.5	0.5	0.5	0.5
carbomer	0.4	0.4	0.4	0.4
citric acid	As needed, pH 4.5-6.5
sodium hydroxide	As needed, pH 4.5-6.5
Colorant	As needed

Example 21

Shampoo Compositions

Example	21a	21b	21c	21d
Ingredient	wt %	wt %	wt %	wt %
Aqua	To 100	To 100	To 100	To 100
Piroctone	0.1	0.3	0.7	1.0
sodium laureth sulfate	15	15	15	15
coco-betaine	3	3	3	3
glycol distearate	2.5	2.5	2.5	2.5
sodium chloride	2	2	2	2
PPG-5-ceteth-20	1.8	1.8	1.8	1.8
Hair conditioning agent	1.5	1.5	1.5	1.5
octyldodecanol	1	1	1	1
carbomer	1	1	1	1
guar hydroxypropyltrimonium	1	1	1	1
chloride
sodium hyaluronate	0.4	0.4	0.4	0.4
citric acid	As needed, pH 4.5-6.5
sodium hydroxide	As needed, pH 4.5-6.5
Colorant	As needed

Example 22

Bar shampoos

	Example	22a	22b	22c	22d
	Ingredient	wt.-%	wt.-%	wt.-%	wt.-%
	Piroctone	0.3	0.5	1.0	0.1
	Sodium Methyl Cocoyl Taurate	6	6	6	6
	Sodium Cocoyl Isethionate	60.5	60.5	60.5	60.5
	Cocamidopropyl Betaine	3	3	3	3
	PEG-180	25	25	25	25
	Quaternium-98	4	4	4	4
	(Genadvance Repair)
	Parfum	0.5	0.5	0.5	0.5
	Preservative	As needed

Claims

1-13. (canceled)

14. A process for the preparation of a compound of formula (I)

15. The process according to claim 14, wherein R1 is H, a linear or branched C1-C12-alkyl, or a cyclohexyl; andR2 is H or a linear or branched C1-C4-alkyl.

16. The process according to claim 14, wherein the compound of formula (II) is reacted with a hydroxylammonium compound.

17. The process according to claim 16, wherein the hydroxylammonium compound is selected from hydroxylammonium sulfate, hydroxylammonium chloride, and hydroxylammonium acetate.

18. The process according to claim 14, wherein the compound of formula (II) is reacted with hydroxylamine or the hydroxylammonium compound in the presence of a base.

19. The process according to claim 18, wherein the base is selected from alkali metal carbonates, alkali metal hydrogen carbonates, alkali metal hydroxides, and mixtures thereof.

20. The process according to claim 14, wherein the compound of formula (II) is reacted with hydroxylamine or the hydroxylammonium compound in the presence of a solvent.

21. The process according to claim 20, wherein the solvent comprises at least 80 wt.-% of an organic solvent, based on the total weight of the solvent.

22. The process according to claim 21, wherein the organic solvent is selected from heptane, hexane, cyclohexane, methylcyclohexane, toluene, 2-aminopyridine, and mixtures thereof.

23. The process according to claim 14, wherein the compound of formula (II) is reacted with hydroxylamine or the hydroxylammonium compound at a temperature of 60 to 100° C.

24. The process according to claim 14, wherein in step b) the compound of formula (I) is crystallized from the organic solvent.

25. The process according to claim 14, wherein the organic solvent used in step b) is selected from heptane, hexane, cyclohexane, methylcyclohexane, dimethylcyclohexane, and mixtures thereof.

26. The process according to claim 14, wherein in step b) the compound of formula (I) is crystallized or precipitated at a temperature of 0 to 25° C.