JP2008133216A - Hair conditioning composition - Google Patents

Abstract

<P>PROBLEM TO BE SOLVED: To provide a hair conditioning composition excellent in touch feeling in use including stickiness, moistness, smoothness, pliability and firmness. <P>SOLUTION: The hair conditioning composition comprises a block-type alkylene oxide derivative of a specific structure represented by formula (I): Y-[O(EO)<SB>a</SB>-(AO)<SB>b</SB>-(EO)<SB>c</SB>-R]<SB>k</SB>, a cationic surfactant and a polyethylene glycol with a molecular weight of 1,000,000-5,000,000. In formula (I), Y is a residue resulting from removing the hydroxy groups of a polyhydric alcohol having 3-6 hydroxy groups; k is the number of the hydroxy groups in the polyhydric alcohol; EO is an oxyethylene group; AO is 3-6C oxyalkylene groups which are added to one another in a blocked fashion; a×k, b×k adn c×k are the average addition numbers of moles of the oxyethylene groups, 3-6C oxyalkylene groups and oxyethylene groups, respectively, being 0-100, 1-100, and 0-100, respectively, wherein (a+c)×k>1; the ratio of the total oxyethylene groups in formula (I) to the sum of the 3-6C oxyalkylene groups and the total oxyethylene groups in formula (I) is 10-80 mass%; and R is a 1-4C hydrocarbon group. <P>COPYRIGHT: (C)2008,JPO&INPIT

Description

  The present invention relates to an improved use feeling of a hair conditioning composition, in particular a hair conditioning composition comprising a block-type alkylene oxide derivative as an active ingredient.

  Hair washing products such as shampoos are mainly composed of an anionic surfactant, so not only the hair stains but also the oil that protects the hair surface is removed at the same time, and the hair feels smooth. Moist feeling may be lost, and combing may worsen. Therefore, for the purpose of preventing such harmful effects, hair conditioning compositions such as hair rinses, hair treatments, hair conditioners and the like, which contain a cationic surfactant as a main component, have been widely used. This is because the cationic surfactant adsorbs to the keratin protein of the hair, softens the hair, improves the combing and has a bactericidal effect.

  Quaternary ammonium salts have been frequently used as the cationic surfactant to be blended in the hair conditioning composition as described above. However, even in a hair cosmetic containing a quaternary ammonium salt, the usability such as smoothness and moisturizing given to the hair is not sufficiently satisfactory, and when the amount of the quaternary ammonium salt is increased, There are concerns about problems related to irritation to the human body such as eyes and skin.

In order to address the above-described problems of hair conditioning compositions using quaternary ammonium salts, attempts have been made to incorporate a cationic surfactant having an amidoamine structure into the hair conditioning composition. For example, a composition containing lactate or alkyl benzene sulfonate of stearylamidoamine (see, for example, Patent Document 1), a composition containing an amidoamine compound and a carboxylic acid compound (see, for example, Patent Document 2), amidoamine A composition containing a compound and a phosphate ester compound (see, for example, Patent Document 3), an amidoamine compound, a bis (2-alkyl-N-hydroxyethylimidazoline) chloroacetic acid complex type amphoteric surfactant and a polymeric silicone Compositions to be contained (see, for example, Patent Document 4) have been proposed.
However, even in such a composition, although the problem of irritation to the human body is solved as compared with the case of the quaternary ammonium salt, it is sufficiently satisfactory in terms of a smooth feeling and moist feeling on the hair. The effect which should have been not obtained.

  On the other hand, it has been proposed to add smoothness to the hair by further blending silicone oil into the hair conditioning composition. As silicone oils suitable for this purpose, methylpolysiloxane, methylphenylpolysiloxane, and polyether-modified polysiloxane are known. However, the hair conditioning composition blended with the silicone oil can give a smooth feeling to the hair, but there are problems such as a feeling of stickiness and stickiness and a tendency to lose a moist feeling.

  In recent years, it has been reported that when a specific alkylene oxide derivative is blended, moist feeling and stickiness after use are improved during use (see, for example, Patent Document 5). However, the firmness and firmness of the hair after use cannot be said to be sufficiently satisfactory, and further improvement has been desired.

Japanese Patent Publication No. 48-1880 JP-A-62-51612 JP 62-51611 A JP-A-2-160714 Japanese Patent No. 3794576

  The present invention has been made in view of the above-mentioned circumstances, and its problem is to provide a hair conditioning composition excellent in use feeling, in particular, sticky feeling, moist feeling, smooth feeling, supple feeling, and firmness and firmness. There is.

  As a result of intensive studies by the present inventors in order to solve the above problems, a hair conditioning composition comprising a block-type alkylene oxide derivative having a specific structure, a cationic surfactant, and polyethylene glycol having a molecular weight of 1,000,000 to 5,000,000. When it is formulated into a product, it has been found that there is no stickiness to the hair, a moist feeling is given, and an excellent feeling of use that improves smoothness, firmness and firmness is demonstrated, and the present invention has been completed. It was.

（式中、Ｙは３〜６個の水酸基を有する多価アルコールの水酸基を除いた残基、ｋは前記多価アルコールの水酸基数、ＥＯはオキシエチレン基、ＡＯは炭素数３〜６のオキシアルキレン基でそれぞれブロック状に付加されている。ａ×ｋ、ｂ×ｋおよびｃ×ｋはそれぞれオキシエチレン基、炭素数３〜６のオキシアルキレン基、オキシエチレン基の平均付加モル数であり、０≦ａ×ｋ≦１００、１≦ｂ×ｋ≦１００、０≦ｃ×ｋ≦１００、ただし（ａ＋ｃ）×ｋ＞１である。式（Ｉ）中の全オキシエチレン基と炭素数３〜６のオキシアルキレン基の合計に対する、式（Ｉ）中の全オキシエチレン基の割合は、１０〜８０質量％である。Ｒは炭素数１〜４の炭化水素基である。） That is, the hair conditioning composition of the present invention contains a block-type alkylene oxide derivative having a specific structure represented by the following formula (I), a cationic surfactant, and polyethylene glycol having a molecular weight of 1,000,000 to 5,000,000. Features.

(In the formula, Y is a residue obtained by removing a hydroxyl group of a polyhydric alcohol having 3 to 6 hydroxyl groups, k is the number of hydroxyl groups of the polyhydric alcohol, EO is an oxyethylene group, and AO is an oxy of 3 to 6 carbon atoms. Each of which is added in the form of a block with an alkylene group, wherein a × k, b × k and c × k are the average number of moles of oxyethylene group, oxyalkylene group having 3 to 6 carbon atoms, and oxyethylene group, 0 ≦ a × k ≦ 100, 1 ≦ b × k ≦ 100, 0 ≦ c × k ≦ 100, where (a + c) × k> 1 In the formula (I), all oxyethylene groups and 3 to 3 carbon atoms The ratio of all oxyethylene groups in formula (I) to the total of 6 oxyalkylene groups is 10 to 80% by mass, and R is a hydrocarbon group having 1 to 4 carbon atoms.

In the hair conditioning composition, it is preferable that the AO group of the block-type alkylene oxide derivative represented by the formula (a) and the formula (I) is an oxybutylene group.
In the hair conditioning composition, (a) in the block type alkylene oxide derivative represented by the formula (I) is 0, and the addition order of AO and EO is (AO)- (EO) is preferred.
Moreover, in the said hair conditioning composition, it is suitable to mix | blend 0.01-10 mass% of block-type alkylene oxide derivatives shown by said (a) Formula (I).

（式中、Ｒ^１は炭素数１４〜２２のアルキル基又はヒドロキシル基を表し、Ｒ^２，Ｒ^３及びＲ^４は、それぞれ独立に炭素数１〜３のアルキル基、ヒドロキシル基又はベンジル基を表し、Ｘはハロゲン原子又は炭素数１〜２のアルキル硫酸基を表す。） In the hair conditioning composition, it is preferable that the (b) cationic surfactant is a quaternary ammonium salt represented by the following general formula (II).

(In the formula, R ¹ represents an alkyl group having 14 to 22 carbon atoms or a hydroxyl group, and R ² , R ³ and R ⁴ each independently represents an alkyl group having 1 to 3 carbon atoms, a hydroxyl group or a benzyl group. , X represents a halogen atom or an alkyl sulfate group having 1 to 2 carbon atoms.)

（式中、Ｒ^５は炭素数１３〜２３の高級脂肪酸の残基を表し、Ｒ^６は炭素数１〜４のアルキル基を表し、ｎは２〜４の整数を表す。）
前記毛髪コンディショニング組成物において、さらに油分を含有することを特徴とする。
前記油分が液体油脂、固体油脂、ロウ類、炭化水素油、高級脂肪酸、高級アルコール、合成エステル油、シリコーン油からなる群より選択される１種または２種以上であることが好適である。 In the hair conditioning composition, it is preferable that (b) the cationic surfactant is an amidoamine compound represented by the following general formula (III) or an acid addition salt thereof.

(In the formula, R ⁵ represents a residue of a higher fatty acid having 13 to 23 carbon atoms, R ⁶ represents an alkyl group having 1 to 4 carbon atoms, and n represents an integer of 2 to 4).
The hair conditioning composition further comprises an oil.
The oil component is preferably one or more selected from the group consisting of liquid oils, solid oils, waxes, hydrocarbon oils, higher fatty acids, higher alcohols, synthetic ester oils, and silicone oils.

  According to the present invention, a blocky alkylene oxide derivative having a specific structure, a cationic surfactant, and polyethylene glycol having a molecular weight of 1,000,000 to 5,000,000 are blended in a hair conditioning composition, thereby making it feel sticky to hair. It is possible to obtain a hair conditioning composition having an excellent feeling of use that gives a moist feeling and improves a smooth feeling, a supple feeling, and a firmness and firmness.

Hereinafter, preferred embodiments of the present invention will be described.
(A) Block-type alkylene oxide derivative The hair conditioning composition according to the present invention comprises a block-type alkylene oxide derivative having a specific structure represented by the following formula (I).

In the block-type alkylene oxide derivative represented by the above formula (I), Y is a residue obtained by removing a hydroxyl group of a polyhydric alcohol having 3 to 6 hydroxyl groups, k is the number of hydroxyl groups of the polyhydric alcohol, and 3 ~ 6. Examples of the compound having 3 to 6 hydroxyl groups include glycerin with k = 3, trimethylolpropane, hexylene glycol, erythritol with k = 4, pentaerythritol, xylitol with k = 5, sorbitol with k = 6 And inositol. The block-type alkylene oxide derivative to be blended in the hair conditioning composition according to the present invention is basically based on a residue excluding the hydroxyl group of one or a mixture of two or more polyhydric alcohols having 3 to 6 hydroxyl groups. The skeleton.
In the present invention, Y is more preferably a residue obtained by removing a hydroxyl group of a polyhydric alcohol having 3 to 4 hydroxyl groups, that is, it is preferable that 3 ≦ k ≦ 4 is satisfied. When k is 2 or less, when blended in a hair conditioning composition, the smoothness during use and after use tends to be inferior, and when k is 7 or more, a sticky feeling tends to occur.

  EO is an oxyethylene group having 2 carbon atoms. AO is an oxyalkylene group having 3 to 6 carbon atoms, and specific examples include an oxypropylene group, an oxybutylene group, an oxyisobutylene group, an oxy t-butylene group, an oxypentylene group, and an oxyhexylene group. . Preferred are an oxypropylene group and an oxybutylene group, and more preferred is an oxybutylene group.

  b × k is the average added mole number of AO, and 1 ≦ b × k ≦ 100, preferably 3 ≦ b × k ≦ 70. a × k and c × k are average added moles of EO, 0 ≦ a × k ≦ 100, 0 ≦ c × k ≦ 100, preferably 3 ≦ a × k ≦ 70, 3 ≦ c × k ≦ 70. Moreover, the preferable range of the average addition mole number of all the oxyethylene groups in the said formula (I) is 1 <(a + c) * k <= 200, More preferably, it is 6 <= (a + c) * k <= 140. AO becomes a hydrophobic site in the block-type alkylene oxide derivative according to the present invention, and when b × k is 0, it tends to be inferior in stability when blended into a hair conditioning composition. There is a tendency to be inferior in smoothness when dried. In addition, when a × k or c × k is 0, the smoothness during use and after use tends to decrease when blended into a hair conditioning composition, and when it exceeds 100, there is a tendency to cause stickiness. .

The ratio of the total EO in the said formula (I) with respect to the sum total of AO and EO in the said formula (I) is 10-80 mass%, More preferably, it is 20-70 mass%. If it is less than 10% by mass, the moistness during use and after use tends to be lost, and if it is more than 80% by mass, a sticky feeling is produced and the smoothness tends to decrease.
The addition form of AO and EO is block-like, and the addition order is (AO)-(EO) order, (EO)-(AO) order, (EO)-( Any of the order of AO)-(EO) may be sufficient. In the present invention, the order of (AO)-(EO) with respect to Y in the formula is particularly preferable. In the order of (AO)-(EO) with respect to Y in the formula, it corresponds to a in the formula being 0.

  R is a hydrocarbon group having 1 to 4 carbon atoms. Examples of the hydrocarbon group include a methyl group, an ethyl group, an n-propyl group, an isopropyl group, an n-butyl group, a sec-butyl group, and a tert-butyl group. It is done. In the present invention, a methyl group and an ethyl group are preferable. If the carbon number is greater than 5, the moist feeling during use and after use tends to be lost. Further, in the block-type alkylene oxide derivative blended in the hair conditioning composition according to the present invention, R may be the same or different in one molecule, and the block type having the same R in one molecule. One kind of alkylene oxide derivative or a mixture of two or more kinds having different Rs may be used.

Specific examples of the block-type alkylene oxide derivative blended in the hair conditioning composition of the present invention include POB (30) POE (30) glyceryl trimethyl ether, POB (30) POE (35) glyceryl trimethyl ether, POB ( 17) POE (28) glyceryl trimethyl ether, POB (27) POE (45) glyceryl trimethyl ether, POB (14) POE (34) glyceryl trimethyl ether, POB (22) POE (55) glyceryl trimethyl ether, POB (19) POE (55) glyceryl trimethyl ether, POB (40) POE (80) glyceryl trimethyl ether, POB (80) POE (40) glyceryl trimethyl ether, POB (30) POE (30) glycerin Triethyl ether, POB (30) POE (35) glyceryl triethyl ether, POB (14) POE (34) glyceryl triethyl ether, POB (30) POE (30) glyceryl tripropyl ether, POE (30) POP (30) glyceryl trimethyl Examples include ether, POE (35) POP (40) glyceryl trimethyl ether, POE (41) POP (48) glyceryl trimethyl ether, and the like.
The POE, POP, and POB are abbreviations for polyoxyethylene, polyoxypropylene, and polyoxybutylene, respectively, and may be abbreviated as follows.

  The block-type alkylene oxide derivative blended in the hair conditioning composition according to the present invention can be produced by a known method. For example, it is obtained by subjecting a polyhydric alcohol having a hydroxyl group to addition polymerization of ethylene oxide and an alkylene oxide having 3 to 6 carbon atoms, and then subjecting an alkyl halide to an ether reaction in the presence of an alkali catalyst.

  In the hair conditioning composition according to the present invention, the blending amount of the block-type alkylene oxide derivative having the above-mentioned specific structure is preferably 0.01 to 10% by mass, more preferably 0.1 to 0.1% by mass. 5 mass% is preferred. If it is less than 0.01% by mass, the effect of the blending may not be sufficiently exhibited. If it exceeds 10% by mass, a sticky feeling tends to occur after use.

上記式（II）中、Ｒ^１は炭素数１４〜２２のアルキル基又はヒドロキシル基を表し、Ｒ^２，Ｒ^３及びＲ^４は、それぞれ独立に炭素数１〜３のアルキル基、ヒドロキシル基又はベンジル基を表す。また、Ｘはハロゲン原子又は炭素数１〜２のアルキル硫酸基を表す。 (B) Cationic surfactant The hair conditioning composition concerning this invention contains the quaternary ammonium salt shown by following formula (II) as a cationic surfactant.

In the above formula (II), R ¹ represents an alkyl group having 14 to 22 carbon atoms or a hydroxyl group, and R ² , R ³ and R ⁴ are each independently an alkyl group having 1 to 3 carbon atoms, a hydroxyl group or benzyl. Represents a group. X represents a halogen atom or an alkyl sulfate group having 1 to 2 carbon atoms.

  Examples of the quaternary ammonium salt include cetyltrimethylammonium chloride, stearyltrimethylammonium chloride, behenyltrimethylammonium chloride, behenyldimethylhydroxyethylammonium chloride, stearyldimethylbenzylammonium chloride, cetyltriethylammonium methylsulfate, and the like.

上記式（III）中、Ｒ^５は炭素数１３〜２３の高級脂肪酸の残基を表し、Ｒ^６は炭素数１〜４のアルキル基を表す。またｎは２〜４の整数を表す。 Further, the hair conditioning composition according to the present invention contains an amidoamine compound represented by the following formula (III) or an acid addition salt thereof in addition to the quaternary ammonium salt described above as a cationic surfactant. May be.

In the above formula (III), R ⁵ represents a residue of a higher fatty acid having 13 to 23 carbon atoms, and R ⁶ represents an alkyl group having 1 to 4 carbon atoms. N represents an integer of 2 to 4.

  Examples of the amidoamine compounds include stearic acid diethylaminoethylamide, stearic acid dimethylaminoethylamide, palmitic acid diethylaminoethylamide, palmitic acid dimethylaminoethylamide, myristic acid diethylaminoethylamide, myristic acid dimethylaminoethylamide, and behenic acid diethylamino acid. Ethylamide, behenic acid dimethylaminoethylamide, stearic acid diethylaminopropylamide, stearic acid dimethylaminopropylamide, palmitic acid diethylaminopropylamide, palmitic acid dimethylaminopropylamide, myristic acid diethylaminopropylamide, myristic acid dimethylaminopropylamide, behenine Acid diethylaminopropylamide, dimethyl behenate Mino propyl amide.

  The acid addition salt of the amidoamine compound blended in the hair conditioning composition of the present invention is a compound obtained by neutralizing the above amidoamine compound with a normal acid, and reacts the amidoamine compound with the acid. Can be easily manufactured. Examples of the acid used for the production of such an acid addition salt of an amidoamine compound include, for example, low molecular weight aliphatic carboxylic acids such as acetic acid, lactic acid, citric acid and succinic acid, and inorganic such as hydrochloric acid, sulfuric acid, phosphoric acid and nitric acid. Examples thereof include aromatic carboxylic acids such as acid, toluenesulfonic acid, dodecylbenzenesulfonic acid, and benzoic acid. In addition, when neutralized with an acid that is not soluble in water such as a higher fatty acid, the acid addition salt of the product amidoamine compound becomes a water-insoluble salt, which is not preferable because it is difficult to add to the hair conditioning composition. .

  It is preferable that the compounding quantity of the cationic surfactant mix | blended with the hair conditioning composition of this invention is 0.1-5 mass% in a hair conditioning composition whole quantity, More preferably, it is 0.6-3 mass%. It is. If it is less than 0.1% by mass, the conditioning effect may not be exhibited. If it exceeds 5% by mass, a sticky feeling after use tends to occur.

(C) Polyethylene glycol having a molecular weight of 1,000,000 to 5,000,000 The hair conditioning composition according to the present invention contains polyethylene glycol having a molecular weight of 1,000,000 to 5,000,000. In the present invention, if the molecular weight of the polyethylene glycol used is less than 1,000,000, it cannot be expected to improve the effect of use feeling during coating and rinsing. Inferior, and productivity is also reduced.

  In the hair conditioning composition according to the present invention, in addition to the (a) block-type alkylene oxide derivative, (c) polyethylene glycol having a molecular weight of 1,000,000 to 5,000,000 is blended, so that good feeling after use is not impaired. In addition, it is possible to obtain a hair conditioning composition having excellent stretch feel on the hair and a smooth feeling upon rinsing.

  Examples of polyethylene glycol having a molecular weight of 1,000,000 to 5,000,000 used in the present invention include commercially available Polyox WSR series (manufactured by Amacol).

  The blending amount of polyethylene glycol having a molecular weight of 1,000,000 to 5,000,000 blended in the hair conditioning composition of the present invention is preferably 0.005 to 5% by mass, more preferably 0.05%, based on the total amount of the hair conditioning composition. It is -2 mass%. If the amount is less than 0.005% by mass, the conditioning effect may not be exhibited. If the amount exceeds 5% by mass, a smooth feeling after use is undesirably exceeded.

  The hair conditioning composition of the present invention comprises an oil component in addition to (a) a block-type alkylene oxide derivative, (b) a cationic surfactant, and (c) polyethylene glycol having a molecular weight of 1,000,000 to 5,000,000. Thus, a hair conditioning composition excellent in use feeling can be obtained. When blending an oil into a hair conditioning composition, it has the effect of improving the feeling of use such as a smooth feeling and moist feeling, but has the problem of causing stickiness, but the block type alkylene oxide derivative, cationic By blending together a surfactant and polyethylene glycol having a molecular weight of 1,000,000 to 5,000,000, these stickiness can be improved.

  Examples of oils to be blended in the hair conditioning composition of the present invention include liquid oils, solid oils, waxes, hydrocarbon oils, higher fatty acids, higher alcohols, synthetic ester oils, and silicone oils.

  Examples of liquid oils include avocado oil, camellia oil, turtle oil, macadamia nut oil, corn oil, mink oil, olive oil, rapeseed oil, egg yolk oil, sesame oil, persic oil, wheat germ oil, southern castor oil, castor oil, linseed oil , Safflower oil, cottonseed oil, eno oil, soybean oil, peanut oil, tea seed oil, kaya oil, rice bran oil, cinnagiri oil, Japanese kiri oil, jojoba oil, germ oil, triglycerin and the like.

  Examples of the solid fat include cacao butter, palm oil, horse fat, hydrogenated palm oil, palm oil, beef tallow, sheep fat, hydrogenated beef tallow, palm kernel oil, pork fat, beef bone fat, owl kernel oil, hydrogenated oil, cattle Leg fats, moles, hydrogenated castor oil and the like.

  Examples of waxes include beeswax, candelilla wax, cotton wax, carnauba wax, bayberry wax, ibota wax, whale wax, montan wax, nuka wax, lanolin, kapok wax, lanolin acetate, liquid lanolin, sugar cane wax, lanolin fatty acid isopropyl, hexyl laurate, and reduced lanolin. , Jojoballow, hard lanolin, shellac wax, POE lanolin alcohol ether, POE lanolin alcohol acetate, POE cholesterol ether, lanolin fatty acid polyethylene glycol, POE hydrogenated lanolin alcohol ether, and the like.

  Examples of the hydrocarbon oil include liquid paraffin, ozokerite, squalane, pristane, paraffin, ceresin, squalene, petrolatum, microcrystalline wax, and the like.

  Examples of the higher fatty acid include lauric acid, myristic acid, palmitic acid, stearic acid, behenic acid, oleic acid, undecylenic acid, toluic acid, isostearic acid, linoleic acid, linolenic acid, eicosapentaenoic acid (EPA), docosahexaenoic acid ( DHA) and the like.

  Examples of higher alcohols include linear alcohols (eg, lauryl alcohol, cetyl alcohol, stearyl alcohol, behenyl alcohol, myristyl alcohol, oleyl alcohol, cetostearyl alcohol); branched chain alcohols (eg, monostearyl glycerin ether (batyl alcohol) ), 2-decyltetradecinol, lanolin alcohol, cholesterol, phytosterol, hexyl decanol, isostearyl alcohol, octyldodecanol and the like.

  Synthetic ester oils include isopropyl myristate, cetyl octanoate, octyldodecyl myristate, isopropyl palmitate, butyl stearate, hexyl laurate, myristyl myristate, decyl oleate, hexyl decyl dimethyloctanoate, cetyl lactate, myristyl lactate Lanolin acetate, isocetyl stearate, isocetyl isostearate, cholesteryl 12-hydroxystearate, ethylene glycol di-2-ethylhexanoate, dipentaerythritol fatty acid ester, monoisostearate N-alkyl glycol, neopentyl glycol dicaprate, apple Acid diisostearyl, di-2-heptylundecanoic acid glycerin, tri-2-ethylhexanoic acid trimethylolpropane, triisostearic acid trimethylo Propane, tetra-2-ethylhexanoate pentaerythritol, glycerol tri-2-ethylhexanoate, glycerol trioctanoate, glycerol triisopalmitate, trimethylolpropane triisostearate, cetyl 2-ethylhexanoate, 2-ethylhexyl palmi Tate, glyceryl trimyristate, glyceride tri-2-heptylundecanoate, castor oil fatty acid methyl ester, oleyl oleate, acetoglyceride, 2-heptylundecyl palmitate, diisobutyl adipate, N-lauroyl-L-glutamic acid-2 -Octyldodecyl ester, di-2-heptylundecyl adipate, ethyl laurate, di-2-ethylhexyl sebacate, 2-hexyldecyl myristate, 2-hexyldecyl palmitate, 2-hexyldecyl adipate Le, diisopropyl sebacate, 2-ethylhexyl succinate, and triethyl citrate.

  Examples of the silicone oil include linear polysiloxanes (for example, dimethylpolysiloxane, methylphenylpolysiloxane, diphenylpolysiloxane, etc.); cyclic polysiloxanes (for example, octamethylcyclotetrasiloxane, decamethylcyclopentasiloxane, dodecamethylcyclohexyl). And silicone resins that form a three-dimensional network structure, various modified polysiloxanes (amino-modified polysiloxane, polyether-modified polysiloxane, alkyl-modified polysiloxane, fluorine-modified polysiloxane, etc.) It is done.

  In addition to the essential components described above, the hair conditioning composition of the present invention usually contains other components used in hair conditioning compositions such as cosmetics and pharmaceuticals, such as humectants, powder components, amphoteric surfactants, nonionic interfaces. Activator, water-soluble polymer, thickener, film agent, UV absorber, sequestering agent, lower alcohol, polyhydric alcohol, sugar, amino acid, organic amine, polymer emulsion, pH adjuster, skin nutrient, Vitamins, antioxidants, antioxidant auxiliaries, fragrances, water and the like can be appropriately blended as necessary, and can be produced by conventional methods according to the intended dosage form. Specific ingredients that can be blended are listed below, and the hair conditioning composition of the present invention can be prepared by blending the above essential blending ingredients and any one or more of the following ingredients.

  Examples of the humectant include propylene glycol, glycerin, 1,3-butylene glycol, xylitol, sorbitol, maltitol, chondroitin sulfate, hyaluronic acid, mucoitin sulfate, caronic acid, atelocollagen, cholesteryl-12-hydroxystearate, sodium lactate And bile salts, dl-pyrrolidone carboxylates, short-chain soluble collagen, diglycerin (EO) PO adducts, Izayoi rose extract, yarrow extract, merirot extract and the like.

  Examples of the powder component include inorganic powders (for example, talc, kaolin, mica, sericite, muscovite, phlogopite, synthetic mica, saucite, biotite, permiculite, magnesium carbonate, calcium carbonate, silicic acid. Aluminum, barium silicate, calcium silicate, magnesium silicate, strontium silicate, metal tungstate, magnesium, silica, zeolite, barium sulfate, calcined calcium sulfate (baked gypsum), calcium phosphate, fluorine apatite, hydroxyapatite, ceramic powder , Metal soap (eg, zinc myristate, calcium palmitate, aluminum stearate), boron nitride, etc .; organic powder (eg, polyamide resin powder (nylon powder), polyethylene powder, polymethyl methacrylate powder, polystyrene Powder, copolymer resin powder of styrene and acrylic acid, benzoguanamine resin powder, polytetrafluoroethylene powder, cellulose powder, etc.); inorganic white pigment (eg, titanium dioxide, zinc oxide, etc.); inorganic red pigment (eg, Iron oxide (Bengara), iron titanate, etc .; Inorganic brown pigments (eg, γ-iron oxide, etc.); Inorganic yellow pigments (eg, yellow iron oxide, loess, etc.); Inorganic black pigments (eg, black oxide) Iron, low-order titanium oxide, etc.); inorganic purple pigments (eg, mango violet, cobalt violet, etc.); inorganic green pigments (eg, chromium oxide, chromium hydroxide, cobalt titanate, etc.); inorganic blue pigments (eg, Pearl pigments (eg titanium oxide coated mica, titanium oxide coated bismuth oxychloride, titanium oxide coated talc, colored oxidation) Tan-coated mica, bismuth oxychloride, fish scale foil, etc.); metal powder pigments (eg, aluminum powder, copper powder, etc.); organic pigments such as zirconium, barium or aluminum lake (eg, red 201, red 202, red 204) No., red 205, red 220, red 226, red 228, red 405, orange 203, orange 204, yellow 205, yellow 401, and blue 404, organic pigments such as red 3 , Red 104, Red 106, Red 227, Red 230, Red 401, Red 505, Orange 205, Yellow 4, Yellow 5, Yellow 202, Yellow 203, Green 3 and Blue No. 1 etc.); natural pigments (for example, chlorophyll, β-carotene, etc.) and the like.

  Examples of amphoteric surfactants include imidazoline-based amphoteric surfactants (eg, 2-undecyl-N, N, N- (hydroxyethylcarboxymethyl) -2-imidazoline sodium, 2-cocoyl-2-imidazolinium hydroxide). Side-1-carboxyethyloxy disodium salt, etc.); betaine surfactants (for example, 2-heptadecyl-N-carboxymethyl-N-hydroxyethylimidazolinium betaine, lauryldimethylaminoacetic acid betaine, alkylbetaine, amide betaine) , Sulfobetaine, etc.).

  Examples of the lipophilic nonionic surfactant include sorbitan fatty acid esters (for example, sorbitan monooleate, sorbitan monoisostearate, sorbitan monolaurate, sorbitan monopalmitate, sorbitan monostearate, sorbitan sesquioleate, Sorbitan trioleate, diglycerol sorbitan penta-2-ethylhexylate, diglycerol sorbitan tetra-2-ethylhexylate); glycerin polyglycerin fatty acids (eg mono cottonseed oil fatty acid glycerin, monoerucic acid glycerin, sesquioleate glycerin, monostearin) Glycerin acid, α, α'-oleic acid pyroglutamate glycerin, monostearic acid glycerin malic acid, etc.); propylene glycol fatty acid esters (eg monostearies) Propylene glycolate, etc.); hardened castor oil derivative; glycerin alkyl ether, etc.

  Examples of hydrophilic nonionic surfactants include POE-sorbitan fatty acid esters (for example, POE-sorbitan monooleate, POE-sorbitan monostearate, POE-sorbitan monooleate, POE-sorbitan tetraoleate). POE sorbite fatty acid esters (eg, POE-sorbite monolaurate, POE-sorbite monooleate, POE-sorbite pentaoleate, POE-sorbite monostearate, etc.); POE-glycerin fatty acid esters (eg, POE- POE-monooleate such as glycerol monostearate, POE-glycerol monoisostearate, POE-glycerol triisostearate); POE-fatty acid esters (eg POE-distearate, POE-monodiolate, ethylene glycol distearate, etc.) POE-alkyl ethers (eg POE- Lauryl ether, POE-oleyl ether, POE-stearyl ether, POE-behenyl ether, POE-2-octyldodecyl ether, POE-cholestanol ether, etc.); Pluronic type (eg, Pluronic, etc.); POE / POP-alkyl ether (For example, POE / POP-cetyl ether, POE / POP-2-decyltetradecyl ether, POE / POP-monobutyl ether, POE / POP-hydrogenated lanolin, POE / POP-glycerin ether, etc.); Tetra POE / Tetra POP-ethylenediamine condensates (eg Tetronic, etc.); POE-castor oil hardened castor oil derivatives (eg POE-castor oil, POE-hardened castor oil, POE-hardened castor oil monoisostearate, POE-hardened castor Oil triisostearate, POE-hardened castor oil monopyroglutamic acid monoisostearic acid diester, POE-hardened castor oil maleic acid, etc.) POE-beeswax lanolin derivatives (eg POE-sorbite beeswax); alkanolamides (eg coconut oil fatty acid diethanolamide, lauric acid monoethanolamide, fatty acid isopropanolamide, etc.); POE-propylene glycol fatty acid ester; POE-alkylamine POE-fatty acid amide; sucrose fatty acid ester; alkyl ethoxydimethylamine oxide; trioleyl phosphate and the like.

  Examples of natural water-soluble polymers include plant-based polymers (for example, gum arabic, gum tragacanth, galactan, guar gum, carob gum, caraya gum, carrageenan, pectin, agar, quince seed (malmello), alge colloid (guckweed extract), starch (Rice, corn, potato, wheat), glycyrrhizic acid); microbial polymers (eg, xanthan gum, dextran, succinoglucan, bullulan, etc.); animal polymers (eg, collagen, casein, albumin, gelatin, etc.), etc. Is mentioned.

  Semi-synthetic water-soluble polymers include, for example, starch polymers (eg, carboxymethyl starch, methylhydroxypropyl starch, etc.); cellulose polymers (methylcellulose, ethylcellulose, methylhydroxypropylcellulose, hydroxyethylcellulose, sodium cellulose sulfate) Hydroxypropylcellulose, carboxymethylcellulose, sodium carboxymethylcellulose, crystalline cellulose, cellulose powder and the like); alginic acid polymers (for example, sodium alginate, propylene glycol alginate, etc.) and the like.

  Synthetic water-soluble polymers include, for example, vinyl polymers (eg, polyvinyl alcohol, polyvinyl methyl ether, polyvinyl pyrrolidone, carboxyvinyl polymer); polyoxyethylene polymers (eg, polyethylene glycol 20,000, 40,000, 60,000). Etc.); acrylic polymers (for example, sodium polyacrylate, polyethyl acrylate, polyacrylamide and the like); polyethyleneimine; cationic polymers and the like.

  Examples of thickeners include gum arabic, carrageenan, caraya gum, gum tragacanth, carob gum, quince seed (malmello), casein, dextrin, gelatin, sodium pectate, sodium alginate, methylcellulose, ethylcellulose, CMC, hydroxyethylcellulose, hydroxypropyl Cellulose, PVA, PVM, PVP, sodium polyacrylate, carboxyvinyl polymer, locust bean gum, guar gum, tamarind gum, cellulose dialkyldimethylammonium sulfate, xanthan gum, magnesium aluminum silicate, bentonite, hectorite, silicate A1Mg (vee gum), Examples thereof include laponite and silicic anhydride.

  Examples of UV absorbers include benzoic acid UV absorbers (eg, paraaminobenzoic acid (hereinafter abbreviated as PABA), PABA monoglycerin ester, N, N-dipropoxy PABA ethyl ester, N, N-diethoxy PABA ethyl ester. N, N-dimethyl PABA ethyl ester, N, N-dimethyl PABA butyl ester, N, N-dimethyl PABA ethyl ester, etc.); anthranilic acid-based UV absorbers (for example, homomenthyl-N-acetyl anthranilate, etc.); Salicylic acid ultraviolet absorbers (for example, amyl salicylate, menthyl salicylate, homomenthyl salicylate, octyl salicylate, phenyl salicylate, benzyl salicylate, p-isopropanol phenyl salicylate, etc.); cinnamic acid ultraviolet absorbers (for example, octylcinnamate, ethyl- 4-isopropyl cinnamate, meth -2,5-diisopropylcinnamate, ethyl-2,4-diisopropylcinnamate, methyl-2,4-diisopropylcinnamate, propyl-p-methoxycinnamate, isopropyl-p-methoxycinnamate, isoamyl-p-methoxy Cinnamate, octyl-p-methoxycinnamate (2-ethylhexyl-p-methoxycinnamate), 2-ethoxyethyl-p-methoxycinnamate, cyclohexyl-p-methoxycinnamate, ethyl-α-cyano-β-phenyl Cinnamate, 2-ethylhexyl-α-cyano-β-phenylcinnamate, glyceryl mono-2-ethylhexanoyl-diparamethoxycinnamate, etc.); benzophenone UV absorbers (for example, 2,4-dihydroxybenzophenone, 2 , 2'-Dihydroxy-4-methoxybenzophenone, 2,2'-dihydroxy-4,4'-dimethoxybenzophenone 2,2 ', 4,4'-tetrahydroxybenzophenone, 2-hydroxy-4-methoxybenzophenone, 2-hydroxy-4-methoxy-4'-methylbenzophenone, 2-hydroxy-4-methoxybenzophenone-5-sulfone Acid salt, 4-phenylbenzophenone, 2-ethylhexyl-4′-phenyl-benzophenone-2-carboxylate, 2-hydroxy-4-n-octoxybenzophenone, 4-hydroxy-3-carboxybenzophenone, etc.); 3- ( 4'-methylbenzylidene) -d, l-camphor, 3-benzylidene-d, l-camphor; 2-phenyl-5-methylbenzoxazole; 2,2'-hydroxy-5-methylphenylbenzotriazole; (2'-hydroxy-5'-t-octylphenyl) benzotriazole; 2- (2'-hydroxy-5'-methylphenylbenzotriazole; dibenzalazine; dianisoylmethane; 4-methoxy-4'-t-butyldiben Irumetan; 5- (3,3-dimethyl-2-norbornylidene) -3-pentan-2-one, and the like.

  Examples of the sequestering agent include 1-hydroxyethane-1,1-diphosphonic acid, 1-hydroxyethane-1,1-diphosphonic acid tetrasodium salt, disodium edetate, trisodium edetate, tetrasodium edetate Sodium citrate, sodium polyphosphate, sodium metaphosphate, gluconic acid, phosphoric acid, citric acid, ascorbic acid, succinic acid, edetic acid, trisodium ethylenediaminehydroxyethyl triacetate and the like.

  Examples of the lower alcohol include ethanol, propanol, isopropanol, isobutyl alcohol, t-butyl alcohol and the like.

  Examples of the polyhydric alcohol include divalent alcohols (for example, ethylene glycol, trimethylene glycol, 1,2-butylene glycol, tetramethylene glycol, 2,3-butylene glycol, pentamethylene glycol, 2-butene-1, 4-diol, hexylene glycol, octylene glycol, etc.); trivalent alcohol (eg, trimethylolpropane); tetravalent alcohol (eg, pentaerythritol, such as 1,2,6-hexanetriol); pentavalent Alcohol (for example, xylitol, etc.); hexavalent alcohol (for example, sorbitol, mannitol, etc.); polyhydric alcohol polymer (for example, diethylene glycol, dipropylene glycol, triethylene glycol, polypropylene glycol, tetraethylene glycol, diglycerin, triglyceride) Lysine, tetraglycerin, polyglycerin, etc.); divalent alcohol alkyl ethers (for example, ethylene glycol monomethyl ether, ethylene glycol monoethyl ether, ethylene glycol monobutyl ether, ethylene glycol monophenyl ether, ethylene glycol monohexyl ether, ethylene glycol) Mono 2-methylhexyl ether, ethylene glycol isoamyl ether, ethylene glycol benzyl ether, ethylene glycol isopropyl ether, ethylene glycol dimethyl ether, ethylene glycol diethyl ether, ethylene glycol dibutyl ether, etc.); dihydric alcohol alkyl ethers (for example, diethylene glycol monomethyl ether) , Diethylene glycol mono Ethyl ether, diethylene glycol monobutyl ether, diethylene glycol dimethyl ether, diethylene glycol diethyl ether, diethylene glycol butyl ether, diethylene glycol methyl ethyl ether, triethylene glycol monomethyl ether, triethylene glycol monoethyl ether, propylene glycol monomethyl ether, propylene glycol monoethyl ether, propylene glycol monobutyl ether , Propylene glycol isopropyl ether, dipropylene glycol methyl ether, dipropylene glycol ethyl ether, dipropylene glycol butyl ether, etc.); dihydric alcohol ether esters (for example, ethylene glycol monomethyl ether acetate, ethyl) Glycol monoethyl ether acetate, ethylene glycol monobutyl ether acetate, ethylene glycol monophenyl ether acetate, ethylene glycol diazinate, ethylene glycol disuccinate, diethylene glycol monoethyl ether acetate, diethylene glycol monobutyl ether acetate, propylene glycol monomethyl ether acetate, propylene Glycol monoethyl ether acetate, propylene glycol monopropyl ether acetate, propylene glycol monophenyl ether acetate, etc.); glycerin monoalkyl ether (eg, xyl alcohol, ceralkyl alcohol, batyl alcohol, etc.); sugar alcohol (eg, maltotriose, Mannito Sucrose, erythritol, glucose, fructose, amylolytic sugar, maltose, amylolytic sugar reducing alcohol, etc.); glycolide; tetrahydrofurfuryl alcohol; POE-tetrahydrofurfuryl alcohol; POP-butyl ether; POP / POE-butyl ether Tripolyoxypropylene glycerol ether; POP-glycerol ether; POP-glycerol ether phosphate; POP-POE-pentaneerythritol ether, polyglycerol and the like.

  Monosaccharides include, for example, tricarbon sugars (eg, D-glyceryl aldehyde, dihydroxyacetone, etc.); tetracarbon sugars (eg, D-erythrose, D-erythrulose, D-treose, erythritol, etc.); pentose sugars (eg, , L-arabinose, D-xylose, L-lyxose, D-arabinose, D-ribose, D-ribulose, D-xylulose, L-xylulose, etc .; hexose (eg, D-glucose, D-talose, D) -Bucicose, D-galactose, D-fructose, L-galactose, L-mannose, D-tagatose, etc.); pentose sugar (eg, aldheptose, heproose, etc.); octose sugar (eg, octulose, etc.); For example, 2-deoxy-D-ribose, 6-deoxy-L-galactose, 6-deoxy-L-mannose, etc .; amino sugar (eg, D-glucosamine, D-galactosamine, shea Acid, Aminouron acid, muramic acid); uronic acid (e.g., D- glucuronic acid, D- mannuronic acid, L- guluronic acid, D- galacturonic acid, L- iduronic acid) and the like.

  Examples of the oligosaccharides include sucrose, gnocyanose, umbelliferose, lactose, planteose, isoliquinoses, α, α-trehalose, raffinose, lycnose, umbilicin, stachyose verbus courses and the like.

  Examples of the polysaccharide include cellulose, quince seed, starch, galactan, dermatan sulfate, glycogen, gum arabic, heparan sulfate, tragacanth gum, keratan sulfate, chondroitin, xanthan gum, guar gum, dextran, keratosulfate, locust bean gum, succinoglucan, etc. Is mentioned.

  Examples of amino acids include neutral amino acids (eg, threonine, cysteine, etc.); basic amino acids (eg, hydroxylysine, etc.) and the like. Examples of amino acid derivatives include acyl sarcosine sodium (lauroyl sarcosine sodium), acyl glutamate, acyl β-alanine sodium, glutathione and the like.

  Examples of the organic amine include monoethanolamine, diethanolamine, triethanolamine, morpholine, triisopropanolamine, 2-amino-2-methyl-1,3-propanediol, and 2-amino-2-methyl-1-propanol. Is mentioned.

  Examples of the polymer emulsion include an acrylic resin emulsion, a polyethyl acrylate emulsion, an acrylic resin liquid, a polyacryl alkyl ester emulsion, a polyvinyl acetate resin emulsion, and a natural rubber latex.

Examples of the pH adjuster include buffers such as lactic acid-sodium lactate, citric acid-sodium citrate, and succinic acid-sodium succinate.
Examples of vitamins include vitamins A, B1, B2, B6, C, E and derivatives thereof, pantothenic acid and derivatives thereof, biotin and the like.
Examples of the antioxidant include tocopherols, dibutylhydroxytoluene, butylhydroxyanisole, gallic acid esters and the like.

  Examples of the antioxidant assistant include phosphoric acid, citric acid, ascorbic acid, maleic acid, malonic acid, succinic acid, fumaric acid, kephalin, hexametaphosphate, phytic acid, and ethylenediaminetetraacetic acid.

  Examples of other components that can be blended include antiseptics (ethyl paraben, butyl paraben, etc.); anti-inflammatory agents (eg, glycyrrhizic acid derivatives, glycyrrhetinic acid derivatives, salicylic acid derivatives, hinokitiol, zinc oxide, allantoin, etc.); Extract, placenta extract, saxifrage extract, arbutin, etc.); various extracts (eg, buckwheat, auren, shikon, peonies, assembly, birch, sage, loquat, carrot, aloe, mallow), iris, grape, yokuinin, loofah, lily , Saffron, nematode, ginger, hypericum, onionis, garlic, capsicum, chimney, red snapper, seaweed, etc.), activator (eg, royal jelly, photosensitizer, cholesterol derivative, etc.); blood circulation promoter (eg, nonyl acid wallenylamide, nicotine) Acid Gyl ester, nicotinic acid β-butoxyethyl ester, capsaicin, gingerone, cantalis tincture, ictamol, tannic acid, α-borneol, nicotinic acid tocopherol, inositol hexanicotinate, cyclandrate, cinnarizine, trazoline, acetylcholine, verapamil, cephalanthin , Γ-oryzanol, etc.); antiseborrheic agents (eg, sulfur, thianthol, etc.); anti-inflammatory agents (eg, tranexamic acid, thiotaurine, hypotaurine, etc.) and the like.

  The hair conditioning composition according to the present invention means any composition used for hair, particularly a composition that imparts a conditioning effect to hair, preferably hair rinse, hair treatment, hair pack, etc. This hair conditioning composition is used as a hair conditioning composition that is applied to the hair and thoroughly rinsed with water after use (rinse).

The present invention will be described more specifically with reference to the following examples. In addition, this invention is not limited by this. The blending amount is expressed in mass% unless otherwise specified. First, the test method and evaluation method employed in each example will be described.
Moreover, the composition of the hair conditioning composition (rinse) used as control is as follows.
Composition of control hair conditioning composition (rinse) (mass%)
(1) Stearyltrimethylammonium chloride 1.0
(2) Cetostearyl alcohol (C16 / C18 = 7/3) 7.0
(3) Dimethylpolysiloxane (20cs) 5.0
(4) Propylene glycol 5.0
(5) Preservative appropriate amount (6) Dye appropriate amount (7) Fragrance appropriate amount (8) Purified water residue

Evaluation (1): No feeling of stickiness An actual use test was conducted by 10 professional panelists, and the hair conditioning composition of the test examples shown below was used to determine the feeling of stickiness of the hair during and after use (after drying), and the above Have the control hair conditioning composition (rinse) be put into practice and have it scored according to the following scoring criteria. Here, the score determination is performed with the cosmetic during cleaning being set to zero. In addition, the average value which divided the sum total of the score by each panel by the panel number of persons was calculated, and it was set as the evaluation result according to the following evaluation criteria.
Scoring criteria +3: No sticky feeling during use and after use as compared to the control hair conditioning composition.
+2: No sticky feeling is felt during and after use as compared to the control hair conditioning composition.
+1: Little sticky feeling during use and after use as compared with the control hair conditioning composition.
0: Neither can be said.
-1: Compared with the control hair conditioning composition, a slightly sticky feeling is felt during and after use.
-2: Feels sticky during and after use as compared to the control hair conditioning composition.
-3: Compared to the control hair conditioning composition, a very sticky feeling is felt during and after use.
Evaluation criteria A: The average value of 10 panel members is +1.5 points or more B: The average value of 10 panel members is 0 points or more and less than 1.5 points C: The average value of 10 panel members is −1.5 More than 0 points and less than 0 points D: The average value of 10 panelists is less than -1.5 points

Evaluation (2): Moist feeling An actual use test was conducted by 10 professional panelists, and the hair conditioning composition of the test examples shown below and the control hair described above were used for moist feeling during use and after use (after drying). Have the conditioning composition (rinse) be put into practice and have it scored according to the following scoring criteria. Here, the score determination is performed with the cosmetic during cleaning being set to zero. In addition, the average value which divided the sum total of the score by each panel by the panel number of persons was calculated, and it was set as the evaluation result according to the following evaluation criteria.
Scoring criteria +3: Compared to the control hair conditioning composition, it feels very moist during and after use.
+2: A moist feeling is felt during and after use as compared to the control hair conditioning composition.
+1: A slightly moist feeling is felt during and after use as compared with the control hair conditioning composition.
0: Neither can be said.
-1: Compared to the control hair conditioning composition, it feels less moist during and after use.
-2: Compared to the control hair conditioning composition, it does not feel moist during use and after use.
-3: Compared to the control hair conditioning composition, no moist feeling is felt during and after use.
Evaluation criteria A: The average value of 10 panel members is +1.5 points or more B: The average value of 10 panel members is 0 points or more and less than 1.5 points C: The average value of 10 panel members is −1.5 More than 0 points and less than 0 points D: The average value of 10 panelists is less than -1.5 points

Evaluation (3): Smoothness An actual use test was conducted by 10 professional panelists, and the hair conditioning composition of the test examples shown below and the control hair described above were used for the smoothness of the hair during and after use (after drying). Have the conditioning composition (rinse) be put into practice and have it scored according to the following scoring criteria. Here, the score determination is performed with the cosmetic during cleaning being set to zero. In addition, the average value which divided the sum total of the score by each panel by the panel number of persons was calculated, and it was set as the evaluation result according to the following evaluation criteria.
Scoring criteria +3: Compared to the control hair conditioning composition, it feels very smooth during and after use.
+2: A smooth feeling is felt during and after use as compared to the control hair conditioning composition.
+1: A slightly smooth feeling is felt during and after use as compared with the control hair conditioning composition.
0: Neither can be said.
-1: Compared to the control hair conditioning composition, it does not feel much smoother during and after use.
-2: Compared with the control hair conditioning composition, it does not feel a smooth feeling during and after use.
-3: Compared to the control hair conditioning composition, no smooth feeling is felt during and after use.
Evaluation criteria A: The average value of 10 panel members is +1.5 points or more B: The average value of 10 panel members is 0 points or more and less than 1.5 points C: The average value of 10 panel members is −1.5 More than 0 points and less than 0 points D: The average value of 10 panelists is less than -1.5 points

Evaluation (4): supple feeling An actual use test was conducted by 10 professional panelists, and the hair conditioning composition of the test example shown below and the control hair described above were used for the supple feeling of hair during use and after use (after drying). Have the conditioning composition (rinse) be put into practice and have it scored according to the following scoring criteria. Here, the score determination is performed with the cosmetic during cleaning being set to zero. In addition, the average value which divided the sum total of the score by each panel by the panel number of persons was calculated, and it was set as the evaluation result according to the following evaluation criteria.
Scoring criteria +3: Feels very supple during and after use compared to the control hair conditioning composition.
+2: A smooth feeling is felt during and after use as compared to the control hair conditioning composition.
+1: A supple feeling is felt during and after use as compared to the control hair conditioning composition.
0: Neither can be said.
-1: Compared to the control hair conditioning composition, it does not feel so supple during use and after use.
-2: Compared to the control hair conditioning composition, it does not feel a supple feeling during and after use.
-3: Compared to the control hair conditioning composition, no supple feeling is felt during and after use.
Evaluation criteria A: The average value of 10 panel members is +1.5 points or more B: The average value of 10 panel members is 0 points or more and less than 1.5 points C: The average value of 10 panel members is −1.5 More than 0 points and less than 0 points D: The average value of 10 panelists is less than -1.5 points

Evaluation (5): firmness and firmness An actual use test was carried out by 10 professional panelists, and the hair conditioning composition of the test examples shown below was used to determine the firmness and firmness of the hair during and after use (after drying). And the above-mentioned control hair conditioning composition (rinse) is put into practice, and the score is determined according to the following scoring standards. Here, the score determination is performed with the cosmetic during cleaning being set to zero. In addition, the average value which divided the sum total of the score by each panel by the panel number of persons was calculated, and it was set as the evaluation result according to the following evaluation criteria.
Scoring criteria +3: Compared to the control hair conditioning composition, a feeling of firmness and firmness is felt during and after use.
+2: A firm and firm feeling is felt during and after use as compared to the control hair conditioning composition.
+1: A slightly firm and firm feeling is felt during and after use as compared to the control hair conditioning composition.
0: Neither can be said.
-1: Compared to the control hair conditioning composition, it does not feel much firmness or firmness during and after use.
-2: Compared with the control hair conditioning composition, it does not feel a firmness or firmness during or after use.
-3: Compared to the control hair conditioning composition, there is no firmness or firmness during use and after use.
Evaluation criteria A: The average value of 10 panel members is +1.5 points or more B: The average value of 10 panel members is 0 points or more and less than 1.5 points C: The average value of 10 panel members is −1.5 More than 0 points and less than 0 points D: The average value of 10 panelists is less than -1.5 points

In the composition shown in the following table, a hair washing composition was prepared by a conventional method, and an evaluation test was performed on the evaluation items (1) to (5).
First, Table 1 below shows the results of a comparative test between a conventional hair conditioning composition and a hair conditioning composition containing a block-type alkylene oxide derivative having a specific structure.
In addition, the block type alkylene oxide derivative in the following table | surface shall have a structure of the following formula | equation (IV). For example, when a + c + e = 30 and b + d + f = 30, they are expressed as (BO) ₃₀ (EO) ₃₀ .

As is clear from the results of Table 1 above, Test Examples 1 to 3 in which other active ingredients were blended with a hair conditioning composition containing a conventional cationic surfactant as an active ingredient in order to impart a hair conditioning effect are: Although relatively good results are obtained compared to the control hair conditioning composition, it is not fully satisfactory. In particular, there was a problem with the firmness and firmness of the hair after use.
In Test Examples 4 and 5 in which an alkylene oxide derivative represented by CH ₃ O — [(EO) ₁₀ / (PO) ₁₀ ] CH ₃ was blended, generally good evaluation results were obtained. However, in Test Example 6 in which a specific block type alkylene oxide derivative having a different structure was blended, an extremely good evaluation result was obtained particularly in the sense of firmness and firmness of the hair.
From the above results, it has been clarified that when a block type alkylene oxide derivative having a specific structure is blended, an extremely excellent result is obtained as compared with a conventional hair conditioning composition.
Therefore, the present inventors examined the alkylene oxide derivative to be blended. The results are shown in Table 2 below.

As is apparent from the results in Table 2 above, Test Example 13 containing an alkylene oxide derivative containing only an oxyethylene part was particularly low in smoothness and inferior in stickiness and firmness. Further, the alkylene oxide derivative blending test example 14 having only the oxybutylene part was particularly bad in stickiness and moist feeling, and inferior in suppleness and firmness.
Furthermore, in Test Example 15 in which an alkylene oxide derivative having a hydrogen terminus was blended, the stickiness and smoothness were not sufficient. Further, when a random type alkylene oxide derivative was blended (Test Example 16), the firmness and firmness were not satisfactory.
On the other hand, in the test example which mix | blended various block type alkylene oxide derivatives mix | blended with Test Examples 7-12, it was excellent in any evaluation of (1)-(5).

As is clear from the above results, when a block-type alkylene oxide derivative having a specific structure is blended into the hair conditioning composition, there is no stickiness before use, after use, moist feeling, smooth feeling, supple feeling, elasticity and firmness. It is possible to make it excellent in feeling.
Next, the influence by the combination of various components mix | blended with a hair conditioning composition was examined. The results are shown in Table 3 below.

  As is apparent from the results of Table 3 above, when the hair conditioning composition of the present invention is blended with a high molecular weight polyethylene glycol in addition to the block type alkylene oxide derivative having a specific structure (molecular weight 2 million), it is moist. A smooth feeling and firmness can be imparted without impairing the feeling of feeling and stickiness. On the other hand, when polyethylene glycol having a molecular weight of 20,000 is blended, such an effect cannot be obtained, and the stickiness is increased by increasing the blending amount. It is thought that the molecular weight of polyethylene glycol needs to be 1 million or more. However, when the molecular weight of polyethylene glycol exceeds 5,000,000, spinnability is generated, and the use feeling when applied to hair tends to deteriorate. Therefore, it is preferable to blend polyethylene glycol having a molecular weight of 1 million to 5 million. In addition to the block-type alkylene oxide derivative having a specific structure and polyethylene glycol having a molecular weight of 1,000,000 to 5,000,000, a polyethylene glycol having a molecular weight of about 20,000 can be blended to such an extent that the effects of the present invention are not impaired. .

  Moreover, although the addition effect of high molecular weight polyethylene glycol is recognized from about 0.005 mass%, it is 0.05 mass% or more especially recognized notably. However, if it exceeds 5% by mass, the smooth feeling tends to decrease, and it is 0.005 to 5% by mass, and more preferably 0.05 to 0.2% by mass.

Next, the present inventors examined a suitable blending amount of a block-type alkylene oxide derivative having a specific structure. The results are shown in Table 4 below.

  As is clear from the results in Table 4 above, generally excellent hair conditioning effects are observed when the blending amount of the block-type alkylene oxide derivative having a specific structure is 0.01 to 10% by mass. In consideration of the feeling of use such as a smooth feeling and a firmness and firmness, 0.1 to 5% by mass is particularly preferable.

Stickiness Improvement Effect Further, the present inventors have found that the block type alkylene oxide derivative has an effect of improving the stickiness found in oils in the process of studying various blends regarding the block type alkylene oxide derivative according to the present invention. That is, in Table 2, even in a test example in which a block-type alkylene oxide derivative having a specific structure is not blended, stickiness caused by oil such as dimethylpolysiloxane is recognized. On the other hand, in the test example in which the block type alkylene oxide derivative having a specific structure is added, the stickiness feeling due to the oil component can be improved rather than simply suppressing the stickiness feeling.

Hereinafter, some synthesis examples of various alkylene oxide derivatives blended in the hair washing composition of the above-described test examples will be shown.
<Synthesis Example 1>
Synthesis of polyoxybutylene (30 mol) polyoxyethylene (30 mol) trimethylglyceryl ether (block type alkylene oxide derivative) 92 g of glycerin and 18 g of potassium hydroxide as a catalyst were charged into the autoclave, and the air in the autoclave was replaced with dry nitrogen. Then, the catalyst was completely dissolved at 140 ° C. with stirring. Next, 2160 g of butylene oxide was dropped with a dropping device and stirred for 2 hours. Subsequently, 1320 g of ethylene oxide was dropped with a dropping device and stirred for 2 hours. Next, 400 g of potassium hydroxide was charged and the inside of the system was replaced with dry nitrogen, and then 300 g of methyl chloride was injected at a temperature of 80 to 130 ° C. and reacted for 5 hours. Thereafter, the reaction composition was taken out from the autoclave, neutralized with hydrochloric acid and adjusted to pH 6 to 7, and treated at a reduced pressure of -0.088 MPa (gauge pressure) at 100 ° C. for 1 hour in order to remove the contained water. Further, filtration was performed to remove the salt generated after the treatment, and a block-type alkylene oxide derivative was obtained.
Samples that were sampled and reacted before reacting with methyl chloride had a hydroxyl value of 49, the alkylene oxide derivative 1 had a hydroxyl value of 0.4, and the ratio of the number of hydrogen atoms to the number of terminal methyl groups was 0.008. An atom is converted to a methyl group.

<Synthesis Example 2>
Synthesis of polyoxyethylene (57 mol) trimethylglyceryl ether (alkylene oxide derivative) 92 g of glycerin and 18 g of potassium hydroxide as a catalyst were charged into an autoclave, and the air in the autoclave was replaced with dry nitrogen, and then stirred at 140 ° C. The catalyst was completely dissolved. Next, 2508 g of ethylene oxide was dropped with a dropping device and stirred for 2 hours. Next, 400 g of potassium hydroxide was charged and the inside of the system was replaced with dry nitrogen, and then 300 g of methyl chloride was injected at a temperature of 80 to 130 ° C. and reacted for 5 hours. Thereafter, the reaction composition was taken out from the autoclave, neutralized with hydrochloric acid and adjusted to pH 6 to 7, and treated at a reduced pressure of -0.088 MPa (gauge pressure) at 100 ° C. for 1 hour in order to remove the contained water. Further, filtration was performed to remove the salt generated after the treatment, and an alkylene oxide derivative was obtained.
Samples which were sampled and reacted before reacting with methyl chloride had a hydroxyl value of 66, and the alkylene oxide derivative 1 had a hydroxyl value of 0.60.009, and the ratio of the number of hydrogen atoms to the number of terminal methyl groups was almost completely hydrogen atoms. Has been converted to a methyl group.

<Synthesis Example 3>
Synthesis of polyoxybutylene (30 mol) polyoxyethylene (30 mol) glyceryl ether (block type alkylene oxide derivative) 92 g of glycerol and 18 g of potassium hydroxide as a catalyst were charged into the autoclave, and the air in the autoclave was replaced with dry nitrogen. Thereafter, the catalyst was completely dissolved at 140 ° C. with stirring. Next, 2160 g of butylene oxide was dropped with a dropping device and stirred for 2 hours. Subsequently, 1320 g of ethylene oxide was dropped with a dropping device and stirred for 2 hours. Thereafter, the reaction composition was taken out from the autoclave, neutralized with hydrochloric acid and adjusted to pH 6 to 7, and treated at a reduced pressure of -0.088 MPa (gauge pressure) at 100 ° C. for 1 hour in order to remove the contained water. Further, filtration was performed to remove the salt generated after the treatment, and a block-type alkylene oxide derivative was obtained.

<Synthesis Example 4>
Synthesis of polyoxybutylene (30 mol) polyoxyethylene (30 mol) tributyl glyceryl ether (block-type alkylene oxide derivative) 92 g of glycerol and 18 g of potassium hydroxide as a catalyst were charged into the autoclave, and the air in the autoclave was replaced with dry nitrogen. Then, the catalyst was completely dissolved at 140 ° C. with stirring. Next, 2160 g of butylene oxide was dropped with a dropping device and stirred for 2 hours. Subsequently, 1320 g of ethylene oxide was dropped with a dropping device and stirred for 2 hours. Next, after charging 800 g of potassium hydroxide and replacing the inside with dry nitrogen, 1200 g of butyl chloride was injected at a temperature of 80 to 130 ° C. and reacted for 5 hours. Thereafter, the reaction composition was taken out from the autoclave, neutralized with hydrochloric acid and adjusted to pH 6 to 7, and treated at a reduced pressure of -0.088 MPa (gauge pressure) at 100 ° C. for 1 hour in order to remove the contained water. Further, filtration was performed to remove the salt generated after the treatment, and a block-type alkylene oxide derivative was obtained.
Samples which were sampled and reacted before reacting with methyl chloride had a hydroxyl value of 50, the alkylene oxide derivative 1 had a hydroxyl value of 1.5, and the ratio of the number of hydrogen atoms to the number of terminal butyl groups was 0.03, indicating that hydrogen was almost completely removed. Atoms are converted to butyl groups.

<Synthesis Example 5>
Synthesis of polyoxybutylene (30 mol) polyoxyethylene (30 mol) glyceryl ether (random alkylene oxide derivative) 92 g of glycerin and 18 g of potassium hydroxide as a catalyst were charged into the autoclave, and the air in the autoclave was replaced with dry nitrogen. Thereafter, the catalyst was completely dissolved at 140 ° C. with stirring. Next, a mixture of 2160 g of butylene oxide and 1320 g of ethylene oxide was dropped with a dropping device and stirred for 2 hours. Next, 400 g of potassium hydroxide was charged and the inside of the system was replaced with dry nitrogen, and then 300 g of methyl chloride was injected at a temperature of 80 to 130 ° C. and reacted for 5 hours. Thereafter, the reaction composition was taken out from the autoclave, neutralized with hydrochloric acid to adjust to pH 6 to 7, and treated at a reduced pressure of -0.088 MPa (gauge pressure) at 100 ° C for 1 hour in order to remove the contained water. Further, filtration was performed to remove the salt generated after the treatment, and a random alkylene oxide derivative was obtained.
Samples which were sampled and reacted before reacting with methyl chloride had a hydroxyl value of 47, the resulting random alkylene oxide derivative 5 compound had a hydroxyl value of 0.5, and the ratio of the number of hydrogen atoms to the number of terminal methyl groups was 0.011. The hydrogen atom is almost completely converted to a methyl group.

（上記式（ＩＶ）中、ａ＋ｃ＋ｅ＝３０、ｂ＋ｄ＋ｆ＝３５、Ｒ^１，Ｒ^２，Ｒ^３はＣＨ_３であり、ＢＯはオキシブチレン基、ＥＯはオキシエチレン基を示す。）
グリセロールモノステアレート １．０
グリセリン ５．０
プロピレングリコール 適 量
色素 適 量
香料 適 量
精製水 残 余
（評価）
このヘアリンスは、毛髪に対してべたつき感がなく、しっとり感を付与し、且つ、なめらか感及びしなやか感を向上させるという優れた使用感触を有するものであった。 Although the formulation example of the hair conditioning composition of this invention is given to the following, the technical scope of this invention is not limited by these. The following hair conditioning composition was prepared according to a conventional method.
Formulation Example 1: Hair rinse Cetyltrimethylammonium chloride 0.6 (mass%)
Cetostearyl alcohol (C16 / C18 = 6/4) 4.0
Dimethylpolysiloxane (5cs) 3.0
Glycerol monostearic acid 1.0
Liquid paraffin 3.0
POB (30) POE (35) Trimethyl glyceryl ether 8.0

(In the above formula (IV), a + c + e = 30, b + d + f = 35, R ¹ , R ² , and R ³ are CH ₃ , BO represents an oxybutylene group, and EO represents an oxyethylene group.)
Glycerol monostearate 1.0
Glycerin 5.0
Propylene glycol appropriate amount Pigment appropriate amount Fragrance appropriate amount Purified water Residue (Evaluation)
This hair rinse did not have a sticky feeling to the hair, gave a moist feeling, and had an excellent feeling of use that improved smoothness and suppleness.

Formulation Example 2: Hair Treatment Cream Behenyltrimethylammonium chloride 3.0 (mass%)
Cetostearyl alcohol (C16 / C18 = 6/4) 6.5
Behenyl alcohol 2.0
Dimethylpolysiloxane (20cs) 3.0
2-Octyldodecanol 2.0
Polyoxyethylene hydrogenated castor oil derivative 0.3
(Ethylene oxide 60 mol adduct)
Polyoxyethylene stearyl ether 1.0
(Ethylene oxide 4 mol adduct)
Soy lecithin 0.5
Liquid paraffin 3.0
POB (32) POE (52) Trimethyl glyceryl ether 5.0
(In the above formula (IV), a + c + e = 32, b + d + f = 52, R ¹ , R ² , and R ³ are CH ₃ , BO represents an oxybutylene group, and EO represents an oxyethylene group.)
Glycerin 10.0
Dipropylene glycol 5.0
Preservative appropriate amount Pigment appropriate amount Fragrance appropriate amount Purified water Residue (Evaluation)
This hair treatment cream did not have a sticky feeling to the hair, gave a moist feeling, and had an excellent feeling of use that improved smoothness and suppleness.

Formulation Example 3: Hair Rinse Stearate Diethylaminoethylamide 0.6 (mass%)
Cetyl alcohol 2.0
Stearyl alcohol 1.0
Dimethylpolysiloxane (5cs) 3.0
Glycerol monostearic acid 1.0
Liquid paraffin 3.0
POB (17) POE (28) Trimethyl glyceryl ether 8.0
(In the above formula (IV), a + c + e = 17, b + d + f = 28, R ¹ , R ² and R ³ are CH ₃ , BO represents an oxybutylene group, and EO represents an oxyethylene group.)
Glycerol monostearate 1.0
Glycerin 5.0
Propylene glycol 5.0
L-glutamic acid 0.6
Preservative appropriate amount Pigment appropriate amount Fragrance appropriate amount Purified water Residue (Evaluation)
This hair rinse did not have a sticky feeling to the hair, gave a moist feeling, and had an excellent feeling of use that improved smoothness and suppleness.

Formulation Example 4: Hair Treatment Cream Stearate Dimethylaminopropylamide 3.0 (mass%)
Cetyl alcohol 6.5
Behenyl alcohol 2.0
Stearic acid 2.0
Dimethylpolysiloxane (20cs) 3.0
2-Octyldodecanol 2.0
Polyoxyethylene hydrogenated castor oil derivative 0.3
(Ethylene oxide 60 mol adduct)
Polyoxyethylene stearyl ether 1.0
(Ethylene oxide 4 mol adduct)
Liquid paraffin 3.0
POB (41) POE (48) trimethyl glyceryl ether 5.0
(In the above formula (IV), a + c + e = 41, b + d + f = 48, R ¹ , R ² , and R ³ are CH ₃ , BO represents an oxybutylene group, and EO represents an oxyethylene group.)
Glycerin 10.0
Dipropylene glycol 5.0
L-glutamic acid 1.0
Preservative appropriate amount Pigment appropriate amount Fragrance appropriate amount Purified water Residue (Evaluation)
This hair treatment cream did not feel sticky to the hair, gave it a moist feeling, and had an excellent feeling of use that improved smoothness and suppleness.

Claims (8)

(A) containing a block-type alkylene oxide derivative having a specific structure represented by the following formula (I), (b) a cationic surfactant, and (c) polyethylene glycol having a molecular weight of 1,000,000 to 5,000,000. A hair conditioning composition characterized.

(In the formula, Y is a residue obtained by removing a hydroxyl group of a polyhydric alcohol having 3 to 6 hydroxyl groups, k is the number of hydroxyl groups of the polyhydric alcohol, EO is an oxyethylene group, and AO is an oxy of 3 to 6 carbon atoms. Each of which is added in the form of a block with an alkylene group, wherein a × k, b × k and c × k are the average number of moles of oxyethylene group, oxyalkylene group having 3 to 6 carbon atoms, and oxyethylene group, 0 ≦ a × k ≦ 100, 1 ≦ b × k ≦ 100, 0 ≦ c × k ≦ 100, where (a + c) × k> 1 In the formula (I), all oxyethylene groups and 3 to 3 carbon atoms The ratio of all oxyethylene groups in formula (I) to the total of 6 oxyalkylene groups is 10 to 80% by mass, and R is a hydrocarbon group having 1 to 4 carbon atoms.   The hair conditioning composition according to claim 1, wherein the AO group of the block type alkylene oxide derivative represented by the formula (I) is an oxybutylene group.   The hair conditioning composition according to claim 1 or 2, wherein (a) a of the block type alkylene oxide derivative represented by the formula (I) is 0, and the addition order of AO and EO is Y in the formula. On the other hand, a hair conditioning composition characterized by being (AO)-(EO).   The hair conditioning composition according to any one of claims 1 to 3, wherein the block-type alkylene oxide derivative represented by the formula (I) (a) is blended in an amount of 0.01 to 10% by mass. Composition. The hair conditioning composition according to any one of claims 1 to 4, wherein (b) the cationic surfactant is a quaternary ammonium salt represented by the following general formula (II). Composition.

(In the formula, R ¹ represents an alkyl group having 14 to 22 carbon atoms or a hydroxyl group, and R ² , R ³ and R ⁴ each independently represents an alkyl group having 1 to 3 carbon atoms, a hydroxyl group or a benzyl group. , X represents a halogen atom or an alkyl sulfate group having 1 to 2 carbon atoms.) The hair conditioning composition according to any one of claims 1 to 4, wherein (b) the cationic surfactant is an amidoamine compound represented by the following general formula (III) or an acid addition salt thereof. Hair conditioning composition.

(In the formula, R ⁵ represents a residue of a higher fatty acid having 13 to 23 carbon atoms, R ⁶ represents an alkyl group having 1 to 4 carbon atoms, and n represents an integer of 2 to 4).   The hair conditioning composition according to any one of claims 1 to 6, wherein the hair conditioning composition further comprises an oil. The hair conditioning composition according to claim 7, wherein the oil is selected from the group consisting of liquid oils, solid oils, waxes, hydrocarbon oils, higher fatty acids, higher alcohols, synthetic ester oils, and silicone oils. A hair conditioning composition comprising two or more types.