Patent Application
20230303930
The field of the present invention concerns a quaternary ammonium salt that can be used as a green alternative to common cationic surfactants.
According to IUPAC, the International Union of Pure and Applied Chemistry, green chemistry means “the invention, design and use of chemicals and processes for reducing or eliminating the use and the production of hazardous substances”. The main objectives of green chemistry include: preventing the production of waste, rather than treating it after it has been produced; minimising the toxicity of the chemicals used; and using renewable raw materials wherever possible.
Quaternary ammonium salts are widely used as cationic surfactants for fabric softeners, anti-electrostatic agents, corrosion inhibitors, hair conditioners, dispersants, germicides, biocides.
Among these quaternary ammonium salts, cetrimonium chloride or behentrimonium chloride are known and are mainly used as cationic surfactants in cosmetic and/or household products. Other types of quaternary ammonium salts acting as cationic surfactants and biocides are the polymers of quaternary ammonium salts such as, for example, silicone cocoamido quat or silicone dimeramido quat.
The products potentially containing quaternary ammonium salts as cationic surfactants are usually used on a daily and/or high frequency basis by consumers. In addition, they come into direct contact with the consumer's skin layer and/or are sometimes inhaled in the form of vapours.
The common quaternary ammonium salts used as cationic surfactants are associated with certain drawbacks, such as:
This becomes particularly relevant when they are included in cosmetic and/or personal cleansing products. For example, quaternary ammonium chloride salts are often characterised by a rotten fishy smell.
In addition, one of the common synthetic processes for quaternary ammonium salts is based on the Menshutkin reaction (or quaternization reaction); the latter involves the use of polar solvents (e.g. methanol, ethanol) and of an alkyl halide for the alkylation of the tertiary amine group; these alkyl halides are commonly synthesised in the laboratory using toxic solvents and/or reagents (e.g. in the presence of pyridine)—a factor that negatively contributes to the eco-sustainability of these salts.
Furthermore, when used in personal cleansing and cosmetic products, they tend to accumulate at the skin level (mainly cetrimonium chloride or CTAC) and to cause damage to the most superficial skin layer, promoting the onset of skin irritation and/or sensitisation phenomena, especially if used on a high frequency basis; they are sometimes responsible for inducing dehydration phenomena of the skin layer.
The Applicant has synthesised a quaternary ammonium salt that solves the problems of the prior art. The object of the present invention is a quaternary ammonium salt of formula (I)
wherein the substituents R5, R6 are independently chosen between hydrogen and a radical R0 wherein the radical R0 consists of the following structure of formula (II)
wherein the substituent R1 is chosen from the group consisting of: hydrogen, methyl, isopropyl, sec-butyl, isobutyl, ethylenemethylthio, benzyl, para-hydroxybenzyl and 3-methylene-1H-indole,
wherein the substituents R2, R3, R4 are independently chosen from the group consisting of: methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, sec-butyl and tert-butyl,
wherein the counteranion mX− is chosen from the group of carboxylic acids consisting of: formic acid, acetic acid, unsaturated monocarboxylic acids, tartaric acid, adipic acid, aldaric acid, oxalic acid, phthalic acid, azelaic acid, sebacic acid, malonic acid, succinic acid, glutaric acid, pimelic acid, maleic acid, malic acid, fumaric acid, suberic acid, citric acid, isocitric acid, fatty acids, amino acids, keto acids and aromatic carboxylic acids,
wherein m is an integer number comprised between 1 and 22,
wherein n is comprised between 2 and 20.
Further object of the present invention are compositions comprising the quaternary ammonium salt of formula (I) as a cationic surfactant. Said compositions may preferably be cosmetic type compositions or cleaning type, softening/conditioning compositions for surface treatment.
The quaternary ammonium salt of formula (I) developed by the Applicant is advantageous over common quaternary ammonium salts (quat) because:
The quaternary ammonium salt of formula (I) can advantageously be used as a cationic surfactant in cosmetic type and personal cleansing compositions. For these purposes it is advantageous because:
In addition, as mentioned above, the quaternary ammonium salt of formula (I) can advantageously be used as a cationic surfactant in compositions for surface treatment, e.g. for household cleaning or cleaning of surfaces in general; in formulations for cleaning fabrics and leathers, in particular in products with softening power. For these purposes it is advantageous because:
Salt of Formula (I)
With reference to formula (I), the invention will be described hereinbelow in more detail, referring where necessary to the preferred embodiment of the invention.
The substituent R1 of the salt of formula (I) is selected from the group consisting of: hydrogen, methyl, isopropyl, sec-butyl, isobutyl, ethylenemethylthio, benzyl, para-hydroxybenzyl and 3-methylene-1H-indole.
It should be noted that, depending on whether the substituents R5 and R6 are equal to hydrogen (—H) or to the radical R0 (formula II), the value of m may change accordingly.
In general, m with reference to the counteranion X− represents the number of molecules of the counteranion contained in the salt of formula (I). Preferably, m is a number such that it guarantees the neutrality of the molecule of the salt of formula (I). In particular, m is an integer number comprised between 1 and 22, preferably comprised between 1 and 12, preferably comprised between 1 and 8, preferably equal to 1 or 2 or 3 or 4 or 5 or 6 or 7.
According to a particularly preferred embodiment, the salt of formula (I), comprises, at most, a number of quaternary ammonium groups equal to 3, irrespective of the value of n. In other words, the quaternary ammonium molecule and its counteranion X− are preferably between them in a stoichiometric ratio equal to 1:1 or alternatively equal to 1:2 or alternatively equal to 1:3, regardless of the value of n.
The following Table 1 shows the structural formulas of the different preferred embodiments of the salt of formula (I) for each substituent R1.
Preferably, R1 is hydrogen; in other words, the preferred embodiment of the salt of formula (I) is (IA).
For each of the embodiments indicated in Table 1 (IA-II), the substituents R2, R3, R4 are independently chosen from the group consisting of methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, sec-butyl and tert-butyl.
According to a preferred embodiment of the salts of formula (IA-II), at least two of the substituents chosen between R2, R3, R4 are equal to each other and preferably chosen from the group consisting of methyl, ethyl, n-propyl, n-butyl (e.g., R2, R4) and the remaining substituent is preferably chosen from the group consisting of methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, sec-butyl and tert-butyl.
According to a preferred embodiment of the salts of formula (IA-II), at least two of the substituents chosen between R2, R3, R4 are equal to each other and preferably methyl (e.g., R2, R4) and the remaining substituent is preferably chosen from the group consisting of methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, sec-butyl and tert-butyl.
The substituents R2, R3 and R4 of the salt of formula (I) are preferably equal to each other and are chosen among the linear substituents: methyl, ethyl, n-propyl, n-butyl.
The substituents R2, R3 and R4 of the salt of formula (I) are preferably equal to each other and consist of the linear methyl substituent.
According to a preferred embodiment, the substituents R2, R3 and R4 of the salt of formula (IA) are equal to each other and consist of the linear methyl substituent.
It should be noted that the considerations made above with reference to the substituents R2, R3, R4 apply to both the quaternary ammonium group of the salt of formula (I) and to the radical R0.
For each of the embodiments indicated in Table 1 (IA-II), the counteranion mX− is chosen from the group of carboxylic acids (in the form of carboxylate ions) consisting of:
It should be noted that fatty acids are defined as saturated or unsaturated aliphatic monocarboxylic acids with a number of carbon atoms ≥4 and ≤20, preferably ≥4 and ≤18.
For the purposes of the present invention, the keto acids are carboxylic acids which contain a ketone residue and which are involved in various biological processes, such as, for example, the process of forming ketone bodies or of glycolysis.
For the embodiment (IA) of the quaternary ammonium salt of the invention, the counteranion X− is preferably chosen from the group of carboxylic acids (in the form of carboxylate ions) consisting of: formic acid, acetic acid, acrylic acid, adipic acid, aldaric acid, oxalic acid, phthalic acid, azelaic acid, sebacic acid, malonic acid, succinic acid, tartaric acid, glutaric acid, pimelic acid, maleic acid, malic acid, fumaric acid, suberic acid, citric acid, isocitric acid, butyric acid, oleic acid, palmitic acid, stearic acid, glutamic acid, aspartic acid, acetoacetic acid, pyruvic acid, levulinic acid, benzoic acid, salicylic acid, cinnamic acid, caffeic acid.
A polyglycerol-n is defined as a polymer consisting of an n number of structural-base units of glycerol; it should be noted that the commonly commercially available polyglycerols-n are mixtures of polyglycerols, comprising 60% or more of the polyglycerol-n of interest in which about 20% of the mixture consists of one or more of its different homologues, i.e., polyglycerols-n with a lower or higher n number of repeating units than the one considered.
In particular, a polyglycerol-n in which n≤10 can be synthesised using green experimental methods starting from natural plant glycerine, following the Cosmos and NaTrue standards.
In contrast, a polyglycerol-n in which n>10 is normally obtained by experimental methods known to the person skilled in the art which include the use of synthetic (non-vegetable) glycerin.
According to a preferred embodiment of the quaternary ammonium salt of formula (I), n is comprised between 2 and 10, preferably comprised between 2 and 6, preferably equal to 2, 3, 4 or 5.
In solution (or mixture), the quaternary ammonium salt of formula (I) is preferably electrically neutral. For the purposes of the present invention, electrically neutral means a molecular structure that contains an equal number of positive charges and of negative charges.
Embodiments in which the substituent R5 is hydrogen and the substituent R6 is hydrogen According to a preferred embodiment of the salt of formula (I), preferably of the salt of formula (IA), the substituent R5 is equal to hydrogen H and the substituent R6 is hydrogen.
In this preferred embodiment, the salt of formula (I), preferably the salt of formula (IA), is characterised by a single positive charge on the quaternary nitrogen N.
According to this preferred embodiment, the value of m is preferably equal to 1. Still preferably, in this first preferred embodiment, the positive charge of the quaternary nitrogen is neutralised by the counteranion mX−, which satisfies the following conditions
It should be noted that, preferably, the degree of ionisation of the pluriprotic carboxylic acid is influenced by the pH conditions of the chemical environment in which the salt of formula (I) is placed, preferably the salt of formula (IA), or to those of the process at which the quaternisation thereof takes place. In fact, although the quaternisation reaction carried out under acid catalysis is advantageous because it uses the carboxylic acid destined to neutralise the quaternary N, the same reaction can also be carried out under alkaline catalysis.
Embodiments in which the Substituent R5 is Equal to the Radical R0 and the Substituent R6 is Hydrogen
According to a preferred embodiment of the salt of formula (I), preferably of the salt of formula (IA), the substituent R6 is hydrogen, the substituent R5 is equal to the radical R0, characterised by the following structure of formula (II):
According to this embodiment, the substituent R1 of R0 is selected from the group consisting of: hydrogen, methyl, isopropyl, sec-butyl, isobutyl, ethylenemethylthio, benzyl, para-hydroxybenzyl and 3-methylene-1H-indole.
Preferably, R1 of R0 is hydrogen; for the substituents R2, R3, R4, the above considerations apply.
According to a particularly preferred embodiment mode of the present embodiment, the substituents R2, R3 and R4 of R0 are equal to each other and consist of the linear methyl substituent.
According to this preferred embodiment, the salt of formula (I), preferably of formula (IA), is characterised by a double positive charge on the corresponding quaternary nitrogen atoms N.
According to this preferred embodiment, the value of m may preferably be equal to 1 or 2. Still preferably, the positive charges of the quaternary nitrogen atoms are neutralised under the following conditions:
Still preferably, when the substituent R5 is equal to R0 and m is equal to 2, the two counteranions X− neutralising the two positive charges of the nitrogen atoms of the salt of formula (I), preferably of formula (IA), may consist of the same carboxylic acid (same entity) or of two carboxylic acids of different nature (different entity).
The Applicant hereinafter describes particularly preferred embodiments of the salt of formula (IA).
Embodiments in which the Substituent R5 and the Substituent R6 are Equal to the Radical R0
According to a preferred embodiment of the salt of formula (I), preferably of the salt of formula (IA), the substituents R6 and R5 are equal to the radical R0 (formula II) and equal to each other.
According to this embodiment, the substituent R1 of R0 is selected from the group consisting of: hydrogen, methyl, isopropyl, sec-butyl, isobutyl, ethylenemethylthio, benzyl, para-hydroxybenzyl and 3-methylene-1H-indole.
Preferably, R1 of R0 is hydrogen; for the substituents R2, R3, R4, the above considerations apply.
According to a particularly preferred embodiment mode of the present embodiment, the substituents R2, R3 and R4 of R0 are equal to each other and consist of the linear methyl substituent.
According to this preferred embodiment, the salt of formula (I), preferably of formula (IA), is characterised by a plurality of positive charges on the corresponding quaternary nitrogen atoms N.
Still preferably, the salt of formula (I), preferably of formula (IA), is characterised by a maximum of 3 quaternary ammonium groups and thus by three positive charges on the corresponding quaternary nitrogen atoms N, irrespective of the value of n.
According to this preferred embodiment, the value of m may preferably be equal to 1 or 2 or 3. Still preferably, the positive charges of the quaternary nitrogen atoms are neutralised under the following conditions:
Still preferably, when the substituent R5 is equal to R0 and m is equal to 2, the two counteranions X− neutralising the two positive charges of the nitrogen atoms of the salt of formula (I), preferably of formula (IA), may consist of the same carboxylic acid (same entity) or of two carboxylic acids of different nature (different entity).
The Applicant hereinafter describes particularly preferred embodiments of the salt of formula (IA).
According to a first preferred embodiment of the salt of formula (IA), the substituents R5 and R6 are both hydrogen, m is equal to 1, the substituent R1 is hydrogen, the substituents R2, R3 and R4 are methyl, as well as in the following formula:
Preferably n is equal to 2, 3, 4 or 5.
According to this first preferred embodiment, the counteranion X− is acetate. The acetate counteranion is particularly advantageous for the purposes of the invention because it gives the quaternary ammonium salt of formula (I) a pleasant fruity smell.
According to a further preferred embodiment of the salt of formula (IA), the substituents R5 and R6 are both hydrogen, m is equal to 1, the substituent R1 is hydrogen, the substituents R2, R3 and R4 are methyl and the counteranion X− is malate, as well as in the following formula (IA2):
Preferably n is equal to 2, 3, 4 or 5.
The Applicant points out that the malate ion as depicted in formula (IA2) is for illustrative purposes only and not limiting the purposes of the invention.
For the purposes of the present invention, the malate is preferably the dicarboxylate ion of the natural enantiomer of the malic acid, namely the L-form (or 2S-hydroxy-1,4-butanedioic acid), which is the one biologically active.
A third embodiment is the quaternary ammonium salt characterised by the following structure formula (IA3), wherein the substituent R5 is equal to the radical R0, R6 is hydrogen, R1 is hydrogen, the substituents R2, R3 and R4 are methyl groups, wherein m is equal to 2 and the counteranion X− is acetate:
Preferably n is equal to 2, 3, 4 or 5.
According to an alternative embodiment of the salt of Formula IA3 X− is the monoionised malate ion or the monoionised tartrate ion and m is equal to 2.
A fourth embodiment of the invention is the quaternary ammonium salt characterised by the following structure formula (IA4), wherein the substituent R5 is equal to the radical R0, R6 is hydrogen, R1 is hydrogen, the substituents R2, R3 and R4 are methyl groups, wherein m is equal to 1 and the counteranion X− is the malate ion or the tartrate ion:
According to this fourth embodiment of structure formula (IA4), n is equal to 2, 3, 4, or 5.
A fifth embodiment of the invention is the quaternary ammonium salt characterised by the following structure formula (IA5), wherein the substituents R5 and R6 are equal to the radical R0, R1 is hydrogen, the substituents R2, R3 and R4 are methyl groups, wherein m is equal to 1 or 3 and the counteranion X− is the citrate ion or the acetate ion:
According to this fourth embodiment of structure formula (IA4), n is equal to 2, 3, 4, or 5. Still preferably, the number of quaternary ammonium groups is equal to 3, regardless of the n value.
The quaternary ammonium salt of formula (I) can be advantageously obtained using the reactions known in the state of the art: by way of example,
It should be noted that, advantageously, water is the only by-product of the synthesis reaction of the quaternary ammonium salt of formula (I); thus, there is no formation and/or potential release of other compounds or chemical derivatives into the environment.
As with the quaternary ammonium salt of formula (IA), the synthesis reaction of the quaternary ammonium salt of formula (I) can be carried out starting from amino acid derivatives characterised by a quaternary amine group at carbon α (N—R2, R3, R4).
Advantageously, the starting amino acid derivative (N—R2, R3, R4), the polyglycerol-n and the organic acid used in these chemical reactions are in turn obtained, as far as possible, by green synthesis methods according to the Cosmos and NaTrue standards and the Regulation (EC) No. 1223/2009, thus contributing to the sustainability of the final product.
Composition Comprising at Least One Salt of Formula (I) as a Cationic Surfactant
The salt of formula (I), preferably of formula (IA), is preferably used as a cationic surfactant.
Preferably, the salt of formula (I) is used as a wetting agent, conditioning/softening, emulsifying, cleaning, antistatic agent.
As already anticipated, further object of the present invention is a composition comprising at least one quaternary ammonium salt formula (I) as a cationic surfactant, in combination with possible excipients and/or diluents.
In the composition claimed preferably the salt of formula (I) is in a concentration comprised between about 0.25% and 7% (w/w), preferably between about 0.25% and 5%, preferably between about 0.5% and 5% (w/w), preferably between about 1% and 5% (w/w), preferably equal to about 0.25%, 0.5%, 1%, 2%, 3%, 4%, 5% (w/w) by weight on the total weight of the composition.
In the composition comprising the salt of formula (I), the latter may be the sole cationic surfactant or may be in combination with other cationic surfactants.
When used in combination with other cationic surfactants (e.g. polymeric cationic surfactants), at the dosages indicated above, the salt of formula (I) enables the use of silicone derivatives to be avoided or the use of other polymeric cations to be reduced.
Cationic surfactants that can be used in combination with the salt of formula (I) are, for example, chosen from the group consisting of: cetrimonium chloride (or CTAC), behentrimonium chloride (or BTAC), stearamidopropyl dimethylamine (or SAPDMA) and guar hydroxypropylthrimethylammonium chloride (or GHPTAC), Dioleylethyl Hydroxyethylmonium Methosulfate (Tetranil CO-40) and Behenoyl PG-Trimonium Chloride (Quartamina BTC-131).
The composition preferably has a pH higher than 3.5 and less than 6.0; preferably the cosmetic composition has a pH comprised between 3.5 and 5, preferably comprised between 4 and 4.5.
The pH of the composition can be regulated by including one or more buffering agents in the composition; an average person skilled in the art, on the basis of his basic knowledge, would be able to select without any difficulty one or more suitable buffering agents for the purpose, choosing among those known to be state of the art.
Cosmetic Composition Comprising the Salt of Formula (I)
According to an embodiment of the invention, the composition comprising the salt of formula (I), preferably of formula (IA), is of the cosmetic type.
The cosmetic composition comprising the salt of formula (I) may further comprise suitable excipients and/or diluents known to the person skilled in the art. By way of example, suitable excipients and/or diluents are selected among: water; cationic surfactants; anionic surfactants; amphoteric surfactants; conditioning agents; active ingredients, e.g. proteins, amino acids, osmoprotectants, vitamins; anti-dandruff agents; thickening agents; viscosity agents; filming agents, emulsifiers; antioxidants; chelators; pigments for hair colouring; buffering agents for pH regulation; natural extracts; fragrances; essential oils; humectants.
The cosmetic composition preferably has a pH higher than 3.5 and less than 6.0; preferably a pH comprised between 3.5 and 5, preferably comprised between 4 and 4.5.
Without wishing to be bound by any theory, the Applicant believes that the pH influences the conditioning capacities of a cationic system; in this sense, at the above-mentioned pH values, the cosmetic composition has shown better conditioning capacities: the hair could be more easily combed than at other pH values of the composition.
The pH of the cosmetic composition can be regulated by including one or more buffering agents in the composition; an average person skilled in the art, on the basis of his basic knowledge, would be able to select without any difficulty one or more suitable buffering agents for the purpose, choosing among those known to be state of the art.
The cosmetic (or cosmetic type) composition is preferably in the form of a cleansing product for the skin and hair, a conditioning product for the hair or a moisturising product for the skin.
When in the form of a cleansing product for the skin and hair, the cosmetic composition is preferably in the form of shampoo, conditioning shampoo (2-in-1), bath foam.
According to a preferred embodiment, the cosmetic composition in the form of a skin and hair cleanser comprises the salt of formula (I) in a concentration comprised between about 1 and 3%.
When in the form of a hair conditioning product, the cosmetic composition is in the form of an oil non oil conditioner or hair conditioner.
According to a preferred embodiment, the cosmetic composition in the form of a hair conditioning product comprises the salt of formula (I) in a concentration comprised between about 1 and 7%.
When in the form of a skin moisturising product, the cosmetic composition is preferably in the form of a moisturising cream.
According to a preferred embodiment, the cosmetic composition in the form of a skin moisturising cream comprises the salt of formula (I) in a concentration comprised between 1 and 3%.
When used as the sole cationic surfactant in hair cosmetic compositions, the quaternary ammonium salt of formula (I) shows comparable or more advantageous effects than common surfactants (see section Example 2).
According to a preferred embodiment, the cosmetic composition is in the form of a hair conditioning product and preferably comprises a fatty alcohol with a number of carbon atoms comprised between 14 and 22, preferably comprised between 16 and 18.
Preferably, the fatty alcohol contained in the composition is chosen from the group consisting of cetyl alcohol, stearyl alcohol or a combination of the foregoing (cetylstearyl alcohol). According to a preferred embodiment, the amount of alcohol is comprised between 1.10% and 2.20% by weight with respect to the amount of salt of formula (I).
The association with fatty alcohols advantageously promotes the combability, reducing the force needed for the operation of combing the hair with a smoother comb passage.
Composition Comprising the Salt of Formula (I) for Surface Treatment
The salt of formula (I), preferably of formula (IA), is preferably used as a cationic surfactant.
Preferably, the salt of formula (I) is used as a wetting agent, conditioning/softening, emulsifying, cleaning, antistatic agent.
A further object of the present invention is a cleaning, softening/conditioning composition for surface treatment.
It should be noted that by surfaces it is intended both the household and non-household surfaces (objects, worktops, floors); leather surfaces; textile or fabric surfaces.
Preferably, the compositions for surface treatment that can be formulated with the quaternary ammonium salt of formula (I) are liquid compositions.
Preferably, the surface treatment comprises cleaning treatments of inert surfaces, leather or textiles, anti-static treatments of inert surfaces or textiles, softening treatments of textiles or leather, treatments for the care or maintenance of inert surfaces, leather or textiles and combinations of the foregoing.
In particular, the composition for surface treatment preferably comprises the salt of formula (I) in combination with any excipients and/or diluents.
It should be noted that diluents suitable for preparing compositions for surface treatment in accordance with the invention include:
It should be noted that organic solvents are generally used in the preparation of compositions for surface treatment when also synthetic surfactants are introduced in addition to the salt of formula (I). In order to make a composition for surface treatment green (hence that does not contain synthetic surfactants), the cetyl alcohol can be used as a solvent.
Composition for surface treatment comprising the salt of formula (I) according to the invention which preferably contains solvents in an amount comprised between 0 and 6% by weight on the total weight of the composition.
Composition for surface treatment comprising the salt of formula (I) according to the invention preferably containing water in an amount comprised between 0 and 95%, preferably between 0 and 90% by weight on the total weight of the composition.
Suitable excipients for the composition for surface treatment in accordance with the invention include, for example: chelators; amphoteric surfactants; cationic surfactants; pH control buffering systems; metal ion control agents; dyes; pigments; smell control agents (such as for example cyclodextrins); perfumes; essential oils; preservatives; anti-microbial agents; anti-mould agents; anti-oxidants; anti-corrosion agents; enzymes; water softening agents, bentonite, zeolite and combinations of the foregoing.
In the composition for surface treatment according to the invention preferably the salt of formula (I) is in a concentration comprised between about 0.25% and 7% (w/w), preferably between about 0.25% and 5%, preferably between about 0.5% and 5% (w/w), preferably between about 1% and 5% (w/w), preferably equal to about 0.25%, 0.5%, 1%, 2%, 3%, 4%, 5% (w/w) by weight on the total weight of the composition.
In the composition for surface treatment, the salt of formula (I) may be the only cationic surfactant or may be in combination with other cationic surfactants.
When used in combination with other cationic surfactants (e.g. polymeric cationic surfactants) or cationic/non-ionic surfactants or non-ionic surfactants, at the dosages indicated above, the salt of formula (I) allows the reduction of other polymeric cations.
Cationic surfactants that can be used in combination with the salt of formula (I) are, for example, chosen from the group consisting of: cetrimonium chloride (or CTAC), behentrimonium chloride (or BTAC), stearamidopropyl dimethylamine (or SAPDMA) and guar hydroxypropylthrimethylammonium chloride (or GHPTAC), Dioleylethyl Hydroxyethylmonium Methosulfate (Tetranil CO-40) and Behenoyl PG-Trimonium Chloride (Quartamina BTC-131).
In the composition for surface treatment, the salt of formula (I) can be used in combination with non-ionic surfactants. Non-ionic surfactants that can be used are preferably chosen among: polyoxyethylene derivatives of fatty acids and alkyl-poly-glucosides or APGs, preferably they are APGs. Preferably, if the composition for surface treatment contains APGs, these may be generically chosen among ethanolamides, ethoxylated amides, ethoxylated amines, ethoxylated acids, cetomacrogol and mixtures thereof, preferably the non-ionic surfactant is chosen among Lauryl Polyglucoside, Cocamido propylamine oxide and mixtures of the foregoing.
The composition for surface treatment has preferably a pH higher than 3.5 and less than 6.0; preferably, the cosmetic composition has a pH comprised between 3.5 and 5, preferably comprised between 4 and 4.5.
Without wishing to be bound by any theory, the Applicant believes that the pH influences the conditioning/softening and anti-static capacities of a cationic system; in this sense, at the above pH values, the composition for surface treatment has shown improved conditioning/softening or anti-static capacities.
The pH of the composition for surface treatment can be regulated by including one or more buffering agents in the composition; an average person skilled in the art, on the basis of his basic knowledge, would be able to select without any difficulty one or more suitable buffering agents for the purpose, choosing among those known to be state of the art.
According to a preferred embodiment, the composition for surface treatment in the form of a detergent comprises the salt of formula (I) in a concentration comprised between 0.25% and 5%, preferably comprised between 0.25% and 2.5%, preferably comprised between 0.5% and 2%, preferably equal to 0.5%, 1%, 1.5% and 2% by weight, on the total weight of the composition (w/w).
When in the form of a conditioning/softening product, the composition comprises the salt of formula (I) in a concentration comprised between 0.5% and 7%, preferably comprised between 0.5% and 6%, preferably comprised between 1.5% and 5.5%, preferably equal to 2%, 2.5% 3%, 3.5%, 4%, 4.% 5% by weight, on the total weight of the composition (w/w).
The Applicant provides hereinbelow examples for illustrative and non-limiting purposes of cosmetic use of the salt of formula (I).
1.1—Conditioning Shampoo
1.2—Conditioning Shampoo (2-in-1)
1.3—Green Conditioning Shampoo (2-in-1)
1.4—Hair Conditioner
1.5—‘Oil not Oil’ Hair Conditioner
1.6—After-Bath Body Cream
2.1—Visual Assessment
In the picture in
2.2—Method for Measuring the Combability
Caucasian hair strands of the same origin were washed for 1 minute with a shampoo and then treated for 1 minute with a hair conditioning product formulated with the quaternary ammonium salt of the invention and with conditioning products formulated with different cationic ingredients (control).
The combability measurements were then carried out with a tensiometer (INSTRON Mod. 5543, speed 500 mm/min) on both wet and dry hair (
In order to facilitate the interpretation of the results obtained by the Applicant, it should be noted that combability means the force that the hair opposes to the sliding of the comb, i.e. the measurement of the resistance that the hair exerts on the passage of the comb.
2.3—Measurement of Dry Detangling of Hair
The graph in
In particular, the hair was combed following the treatment with a conditioning shampoo and the conditioning shampoo of Example 1.1.
2.4—Measurement of the Detangling Capacity on Damaged Caucasian and Chinese Hair
The graph in
In particular, the hair was combed following the treatment with a 5% aqueous solution of salt of formula (IA1) and an equal amount of a 5% aqueous solution of a 50:50 combination of CTAC/BTAC.
The result of the treatment comprising the salt of formula (IA1) shows better and significant benefits in the operation of dry hair combing (method in Example 2.2), if compared to the result obtained with the common quats, such as CTAC or BTAC.
In addition, the action of the salt of formula (IA1) ensures a noticeable moisturising sensation on damaged hair.
2.5—Hair Thickness Measurement Assessed on Five Strands of Hair after 20 Brush Strokes
The assessment was carried out on strands washed with the Green shampoo of example 1.3, compared with two traditional, market-leading products. The results are shown in the graph in
Although the composition with the salt of formula (IA1) is merely for illustrative purposes, the results are fully comparable with the complex and sophisticated compositions of products from major multinational companies containing synthetic ingredients.
2.6—Hair Breakage Measurement after 10 Brush Strokes
The assessment was carried out on strands washed with the Green shampoo of example 1.3, compared with two traditional, market-leading used previously products (Control 1 and Control 2).
The results of this comparison can be seen in the graph in
2.7—Method for Measuring the Electrostatic Charge (Static Charge Build-Up—Lunn & Evans Method).
The same strands of hair used for the combability tests were dried and combed 10 times under standard environmental conditions (20° C., relative humidity RH=30%) and then the static charge (V) was measured with an appropriate sensor (3M Electical Specialties Division, Model 709).
The detection was carried out 10 times and the average of the values obtained was calculated.
From the results shown in the graph in
The electrostatic charge abatement effect is higher when compared to that achieved with market-leading products comprising quaternary monoalkyl linear chains of CTAC and BTAC.
3.1—Composition in the Treatment of Leather, Textile Surfaces or Fabrics
3.2—Composition in the Treatment of Leather, Textile Surfaces or Fabrics
3.3—Composition in the Treatment of Surfaces (Objects, Worktops, Floors)
| Number | Date | Country | Kind |
|---|---|---|---|
| 102020000020212 | Aug 2020 | IT | national |
| 102021000001586 | Jan 2021 | IT | national |
| 102021000009233 | Apr 2021 | IT | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/IB2021/057481 | 8/13/2021 | WO |
