WO2010116940A1 - 毛髪化粧料 - Google Patents
毛髪化粧料 Download PDFInfo
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- WO2010116940A1 WO2010116940A1 PCT/JP2010/055969 JP2010055969W WO2010116940A1 WO 2010116940 A1 WO2010116940 A1 WO 2010116940A1 JP 2010055969 W JP2010055969 W JP 2010055969W WO 2010116940 A1 WO2010116940 A1 WO 2010116940A1
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- Prior art keywords
- acid
- hair
- group
- carbon atoms
- hair cosmetic
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Classifications
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q5/00—Preparations for care of the hair
- A61Q5/12—Preparations containing hair conditioners
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
- A61K8/34—Alcohols
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
- A61K8/34—Alcohols
- A61K8/342—Alcohols having more than seven atoms in an unbroken chain
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
- A61K8/36—Carboxylic acids; Salts or anhydrides thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
- A61K8/36—Carboxylic acids; Salts or anhydrides thereof
- A61K8/361—Carboxylic acids having more than seven carbon atoms in an unbroken chain; Salts or anhydrides thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
- A61K8/36—Carboxylic acids; Salts or anhydrides thereof
- A61K8/368—Carboxylic acids; Salts or anhydrides thereof with carboxyl groups directly bound to carbon atoms of aromatic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/40—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
- A61K8/41—Amines
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/46—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing sulfur
- A61K8/466—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing sulfur containing sulfonic acid derivatives; Salts
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q5/00—Preparations for care of the hair
Definitions
- the present invention relates to hair cosmetics.
- a hair treatment agent such as a hair conditioner is used.
- Such a hair treatment agent is usually mixed with a quaternary ammonium salt type cationic surfactant. Since the quaternary ammonium salt type cationic surfactant has a high effect of imparting flexibility and antistatic properties to hair, it is blended in various hair cosmetics including treatment agents.
- hair makeup containing a hydroxy ether amine compound instead of a quaternary ammonium salt type cationic surfactant.
- Patent Documents 1 and 2) and hair cosmetics Patent Document 3) containing amidoamine are provided.
- hair cosmetics (Patent Documents 4 and 5) containing alkoxypropyldimethylamine are disclosed. Moreover, the hair cosmetics which improve a feeling of use by mix
- the present invention is an invention whose object is to provide means for improving the touch (hereinafter also referred to as touch at the time of application), particularly focusing on the hair feel at the time of applying the conditioner at the time of washing the hair.
- the present inventor has studied to solve the above problems and surprisingly found that this can be solved by providing a hair cosmetic composition having the following constitution.
- the present invention provides a hair cosmetic (hereinafter also referred to as the hair cosmetic of the present invention) containing the following components (1) to (4).
- a hair cosmetic hereinafter also referred to as the hair cosmetic of the present invention
- a hydroxy ether amine compound represented by the following formula (I) is added in an amount of 0.01 to 10% by mass of the cosmetic
- R 1 is a linear or branched alkyl group or alkenyl group having 6 to 24 carbon atoms
- R 2 is a linear or branched hydroxyalkylene group or hydroxyalkylenyl group having 2 to 6 carbon atoms.
- Each of R 3 and R 4 is the same or different and is a hydrogen atom or a linear alkyl group having 1 to 6 carbon atoms.
- the hydroxy ether amine compound (I) is preferably N- (2-hydroxy-3-stearoxypropyl) -N, N-dimethylamine represented by the following formula (II).
- a hair cosmetic that is excellent in hair feel when applying a conditioner during hair washing.
- R 1 which is a linear or branched alkyl group or alkenyl group having 6 to 24 carbon atoms is, for example, hexyl group, heptyl group, octyl group, nonyl group, decyl group, undecyl group, dodecyl group, tridecyl group, tetradecyl group Group, pentadecyl group, hexadecyl group, heptadecyl group, octadecyl group, nonadecyl group, icosyl group, henicosyl group, docosyl group, tricosyl group, tetracosyl group, myristolyl group, palmitoleyl group, oleyl group, linoyl group, linoleyl group, ricinoleyl Group, isostearyl group and the like.
- Examples of the hydroxyalkylene group or hydroxyalkylenyl group R 2 which is a linear or branched divalent group having 2 to 6 carbon atoms include, for example, a hydroxyethylene group, a hydroxytrimethylene group, a hydroxytetramethylene group, Examples thereof include a hydroxypentamethylene group and a hydroxyhexamethylene group.
- R 3 and R 4 are the same or different and are a hydrogen atom or a linear alkyl group having 1 to 6 carbon atoms.
- R 1 is a stearyl group (octadecyl group)
- R 2 is —CH 2 —CH (OH) —CH 2 —
- R 3 and R 4 Are N- (2-hydroxy-3-stearoxypropyl) -N, N-dimethylamine (II), both of which are methyl groups.
- the hydroxy ether amine compound (I) can be produced by a conventional method according to its chemical structure.
- N- (2-hydroxy-3-stearoxypropyl) -N, N-dimethylamine (II) can be produced by a conventional method corresponding to its chemical structure, for example, the method disclosed in Patent Document 1.
- other known methods may be used.
- the blending amount of the hydroxy ether amine compound (I) in the hair cosmetic of the present invention is 0.01 to 10% by mass, preferably 0.1 to 5% by mass of the cosmetic.
- the blending amount is less than 0.01% by mass, the improvement of the feel upon application of the present invention cannot be substantially expected, and the conditioning effect on the hair due to the blending of the hydroxy ether amine compound (I) tends not to be recognized.
- it exceeds 10% by mass the effect of improving the feel at the time of application commensurate with a large amount of compounding is substantially not recognized.
- higher alcohols examples include lauryl alcohol, myristyl alcohol, cetyl alcohol, cetostearyl alcohol, stearyl alcohol, aralkyl alcohol, behenyl alcohol, oleyl alcohol, jojoba alcohol, chimyl alcohol, and batyl alcohol.
- higher fatty acids include lauric acid, myristic acid, palmitic acid, stearic acid, behenic acid, oleic acid, linoleic acid, undecylenic acid, 12-hydroxystearic acid, lanolin fatty acid, and isostearic acid.
- stearyl alcohol is preferable as the higher alcohol
- stearic acid is preferable as the higher fatty acid.
- the blending amount of the higher fatty acid and / or higher alcohol in the hair cosmetic of the present invention is 0.1 to 20% by mass, preferably 1 to 10% by mass of the cosmetic.
- the blending amount is less than 0.1% by mass, the improvement of the touch at the time of application of the present invention cannot be substantially expected, and there is a tendency that the conditioning effect on the hair by blending of higher fatty acid and / or higher alcohol is not recognized.
- it exceeds mass% the effect of improving the feel at the time of application commensurate with the mass blending is substantially not recognized.
- Organic acid having an aromatic ring skeleton (hereinafter also referred to as an aromatic organic acid) that can be blended in the hair cosmetic of the present invention is, for example, salicylic acid (for example, salicylic acid).
- the blending amount of the aromatic organic acid in the hair cosmetic composition of the present invention is not particularly limited, but is preferably 0.1 mol or more, preferably 0.5 to 1 mol, based on the hydroxy ether amine compound (I) described above. It is.
- the upper limit of the blending amount is not particularly limited, but if it exceeds 1 mol, it is difficult to recognize the effect of improving the feel at the time of application commensurate with the increase of the blending amount. There is a tendency to be irritated.
- Water Water can be ion-exchanged water, purified water, tap water, natural water, etc., and can be freely blended according to the dosage form and form of the hair cosmetic of the present invention. Specifically, it is typically blended as the remainder of the blending amount (mass%) of the other essential components described above and the blending amount (mass%) of other components considering the dosage form and form of the hair cosmetic. Is.
- Alcohol having an aromatic ring skeleton The hair cosmetic of the present invention can be further improved in touch when applied by further blending an alcohol having an aromatic ring skeleton.
- the alcohol having an aromatic ring skeleton include phenoxyethanol and benzyl alcohol, but phenoxyethanol is preferred.
- the blending amount of the alcohol having an aromatic ring skeleton in the hair cosmetic of the present invention is 0.01 to 3% by mass, preferably 0.1 to 1% by mass of the cosmetic. If the blending amount is less than 0.01% by mass, further improvement in the feel upon application of the present invention cannot be substantially expected, and it is difficult to further improve the conditioning effect on the hair by blending higher fatty acids and / or higher alcohols. When the amount exceeds 3% by mass, the additional improvement of the touch at the time of application reaches the limit, and the effect commensurate with the increase in the amount of compounding is substantially not recognized.
- the hair cosmetic composition of the present invention may contain other components within the qualitative and quantitative ranges that do not substantially impair the effects of the present invention. it can.
- a cationic surfactant such as alkyltrimethylammonium chloride is exemplified as a general compounding component.
- an anionic surfactant such as alkyl sulfate ester salt, polyoxyethylene alkyl ether sulfate ester salt, acylmethyl taurate, N-acyl glutamate, etc .
- alkyl betaine And amphoteric surfactants such as alkylamide betaines and imidazolinium betaines
- nonionic surfactants such as fatty acid alkanolamines and the like.
- oils other than the above-mentioned higher fatty acids and higher alcohols such as hydrocarbon oils, ester oils and silicone oils, regardless of the form of hair cosmetics; moisturizing such as glycerin, propylene glycol, 1,3-butylene glycol and polyethylene glycol Agents; Conditioning agents such as cationic polymers such as cationized cellulose; Antidandruff agents such as trichlorocarbanilide, sulfur, zinc pyrithione and isopropylmethylphenol; Thickeners; Viscosity modifiers; Emulsifiers; Agents; UV absorbers; antioxidants; antiseptics; powder components; blood circulation promoters, local stimulants, hair follicle activators, anti-androgen agents, antiseborrheic agents, keratolytic agents, bactericides, anti-inflammatory agents, amino acids , Vitamins, herbal extracts and the like; pH adjusting agents; pigments; fragrances; lower alcohols and the like.
- Hair cosmetic of the present invention can be produced according to a method according to the dosage form and form to be selected.
- the product is prepared by dissolving the target ingredient in a solvent such as water, and examples of the product form include hair rinse, hair conditioner, hair treatment, hair shampoo, rinse-in shampoo and the like.
- A There are four or more panels that answered good. ⁇ : Three panelists answered “good”. ⁇ ⁇ : There are two panels that answered good. ⁇ : One panel responded as good. X: The panel which answered that it was favorable is zero.
- ⁇ Test example> A hair rinse having a formulation shown in Table 1 below was prepared by dissolving and mixing the formulation components in purified water. In addition, the results of the above tests are also shown in Table 1. In the table, stearoxyhydroxypropylamine means N- (2-hydroxy-3-stearoxypropyl) -N, N-dimethylamine (II).
- Comparative Example 5 revealed that the feel upon application when the amount of stearyl alcohol (higher alcohol) was less than that of the present invention did not reach the present invention. From Comparative Example 6, it was found that when stearyl alcohol exceeds the provisions of the present invention, the feel upon application is inferior.
- Hair conditioner Compounding component amount (% by mass) (1) N- (2-hydroxy-3-stearoxypropyl) -N, N-dimethylamine 1.5 (2) Taurine 1.0 (3) Salicylic acid 0.5 (4) Stearyl alcohol 5.0 (5) Stearic acid 0.5 (6) Glycerol monostearate 0.5 (7) Pyrrolidone carboxylic acid 0.4 (8) Hydroxyethylurea 0.4 (9) Camellia seed oil 0.1 (10) Highly polymerized polyethylene glycol (Mw 4 million) 0.1 (11) Quaternary ammonium salt (polyquaternium-61) 0.1 (12) Dimethicone (20 mPa ⁇ s) 5.0 (13) Dimethiconol (10,000 mPa ⁇ s) 1.0 (14) Mineral oil 0.3 (15) Octyl palmitate 0.3 (16) Sorbitol 10.0 (17) Diglycerin 3.0 (18) Isoprene glycol 4.0 (19) POE (10) POP (7) dimethyl ether
- ⁇ Manufacturing method> Heat other than purified water to 70 ° C. to melt solids. 70 ° C. water is added with stirring and mixing. Furthermore, it is cooled to room temperature.
- Hair conditioner Compounding component amount (% by mass) (1) N- (2-hydroxy-3-stearoxypropyl) -N, N-dimethylamine 2.5 (2) Stearyl alcohol 6.0 (3) Solid paraffin 0.5 (4) Glycerol monooleate 0.4 (5) p-Toluenesulfonic acid 0.6 (7) Fragrance 0.4 (8) L-arginine 0.2 (9) Dimethicone (1000 mPa ⁇ s) 0.5 (10) Amodimethicone (1000 mPa ⁇ s) 1.0 (11) Dimethiconol (4000 mPa ⁇ s) 2.0 (12) Isocetyl isostearate 1.0 (13) Glycerin 5.0 (14) Isoprene glycol 2.0 (15) POE (35) POP (40) dimethyl ether (block copolymer) 0.3 (16) Cationized cellulose 0.5 (17) Loquat extract 0.2 (18) Methylparaben 0.3 (19) Benzyl alcohol
- ⁇ Manufacturing method> Heat other than purified water to 80 ° C. to melt solids. Add 80 ° C. water with stirring and mixing. Furthermore, it is cooled to room temperature.
- ⁇ Manufacturing method> Heat other than purified water to 70 ° C. to melt solids. 70 ° C. water is added with stirring and mixing. Furthermore, it is cooled to room temperature.
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Abstract
Description
(1)下記式(I)にて表されるヒドロキシエーテルアミン化合物を、化粧料の0.01~10質量%
(2)高級アルコール及び/又は高級脂肪酸を、化粧料の0.1~20質量%
(3)芳香族環骨格を有する有機酸
(4)水
CH3(CH2)16CH2-O-CH2CH(OH)CH2-N(CH3)2 (II)
本発明の毛髪化粧料の必須の配合成分は、上記の(1)~(4)に示す通りである。
炭素数6~24の直鎖若しくは分岐鎖のアルキル基又はアルケニル基であるR1は、例えば、ヘキシル基、ヘプチル基、オクチル基、ノニル基、デシル基、ウンデシル基、ドデシル基、トリデシル基、テトラデシル基、ペンタデシル基、ヘキサデシル基、ヘプタデシル基、オクタデシル基、ノナデシル基、イコシル基、ヘンイコシル基、ドコシル基、トリコシル基、テトラコシル基、ミリストレイル基、パルミトレイル基、オレイル基、リノイル基、リノレイル基、リシノレイル基、イソステアリル基等が挙げられる。また、炭素数2~6の直鎖若しくは分岐鎖の2価基である、ヒドロキシアルキレン基又はヒドロキシアルキレニル基R2としては、例えば、ヒドロキシエチレン基、ヒドロキシトリメチレン基、ヒドロキシテトラメチレン基、ヒドロキシペンタメチレン基、ヒドロキシヘキサメチレン基等が挙げられる。R3及びR4は、上述のように、同一又は異なって水素原子又は炭素数1~6の直鎖アルキル基である。
本発明の毛髪化粧料に配合可能な高級アルコールと高級脂肪酸は、化粧料等の外用組成物一般において用いられているものを、それぞれ1種又は2種以上を選択して用いることができる。高級アルコールと高級脂肪酸を組み合わせて配合することも可能である。
本発明の毛髪化粧料に配合可能な、芳香族環骨格を有する有機酸(以下、芳香族有機酸ともいう)は、例えば、サリチル酸類(例えば、サリチル酸、3-メチルサリチル酸、4-メチルサリチル酸、5-メチルサリチル酸等)、トルエンスルホン酸(例えば、p-トルエンスルホン酸、o-トルエンスルホン酸、m-トルエンスルホン酸)、安息香酸類(安息香酸、2-メチル安息香酸、3-メチル安息香酸、4-メチル安息香酸等)又はナフタレンスルホン酸の塩(2-ナフタレンスルホン酸塩等)が好適であり、これらの芳香族有機酸を必要に応じて1種又は2種以上用いることができる。これらの中でも、サリチル酸類が、特に好適である。
水は、イオン交換水、精製水、水道水、自然水等を用いることが可能であり、本発明の毛髪化粧料の剤形と形態に応じて自由に配合することができる。具体的には、上記の他の必須成分の配合量(質量%)と、毛髪化粧料の剤形と形態を考慮した他の成分の配合量(質量%)の残分として配合することが典型的である。
(1)芳香族環骨格を有するアルコール
本発明の毛髪化粧料には、さらに、芳香族環骨格を有するアルコールを配合することにより、塗布時感触をいっそう向上させることが可能である。この芳香族環骨格を有するアルコールとしては、例えば、フェノキシエタノール、ベンジルアルコール等を挙げることができるが、フェノキシエタノールが好適である。また、芳香族環骨格を有するアルコールの本発明の毛髪化粧料における配合量としては、化粧料の0.01~3質量%、好適には0.1~1質量%である。当該配合量が0.01質量%未満では、本発明の塗布時感触のさらなる向上が実質的に期待できず、高級脂肪酸及び/又は高級アルコールの配合による毛髪に対するコンディショニング効果をさらに向上させることも困難であり、3質量%を超えると、塗布時感触の追加的な向上が限界に達し、配合量の増加に見合った効果が実質的に認められなくなる。
その他、本発明の毛髪化粧料には、必要に応じて、上記以外の成分を、本発明の効果を実質上損なわない質的、量的な範囲内で配合することができる。例えば、本発明の毛髪化粧料が、ヘアコンディショナー又はヘアリンスである場合には、塩化アルキルトリメチルアンモニウム等のカチオン性界面活性剤が一般的な配合成分として例示される。また、本発明の毛髪化粧料がシャンプーである場合には、アルキル硫酸エステル塩、ポリオキシエチレンアルキルエーテル硫酸エステル塩、アシルメチルタウリン酸、N-アシルグルタミン酸塩等のアニオン性界面活性剤;アルキルベタイン、アルキルアミドベタイン、イミダゾリニウムベタイン等の両性界面活性剤;脂肪酸アルカノールアミン等の非イオン性界面活性剤等が特徴的な一般的配合成分として挙げられる。
本発明の毛髪化粧料は、選択する剤形と形態に応じた方法に従って製造することが可能であり、典型的には、上記の必須配合成分と必要な選択的成分を、水等の溶剤に溶解させることにより製造され、その製品形態としては、ヘアリンス、ヘアコンディショナー、ヘアトリートメント、ヘアシャンプー、リンスインシャンプー等が挙げられる。
本発明の毛髪化粧料に関し用いた評価手法を以下に示す。
塗布時感触に関する実使用試験を、女性パネル6名により行った。具体的には、洗髪直後の濡れた毛髪に、試験品(ヘアリンス)を、適量手にとって塗布し、その際の塗布感触を、(1)製剤の毛髪上での伸び、(2)髪のしなやかさ、(3)毛髪のなめらかさ、(4)毛髪のしっとり感、の4項目について下記基準により評価を行った。
○:良好と回答したパネルが3人である。
○△:良好と回答したパネルが2人である。
△:良好と回答したパネルが1人である。
×:良好と回答したパネルが0人である。
下記表1に示す処方のヘアリンスを、当該処方成分を精製水の中に溶解混合することにより調製した。併せて、上記の試験を行った結果も表1に示す。なお、表中、ステアロキシヒドロキシプロピルアミンは、N-(2-ヒドロキシ-3-ステアロキシプロピル)-N,N-ジメチルアミン(II)を意味する。
配合成分 配合量(質量%)
(1)N-(2-ヒドロキシ-3-ステアロキシプロピル)-N,N-ジメチルアミン 1.5
(2)タウリン 1.0
(3)サリチル酸 0.5
(4)ステアリルアルコール 5.0
(5)ステアリン酸 0.5
(6)モノステアリン酸グリセリン 0.5
(7)ピロリドンカルボン酸 0.4
(8)ヒドロキシエチル尿素 0.4
(9)トウツバキ種子油 0.1
(10)高重合ポリエチレングリコール(Mw400万) 0.1
(11)第4級アンモニウム塩(ポリクオタニウム-61) 0.1
(12)ジメチコン(20mPa・s) 5.0
(13)ジメチコノール(1万mPa・s) 1.0
(14)ミネラルオイル 0.3
(15)パルミチン酸オクチル 0.3
(16)ソルビトール 10.0
(17)ジグリセリン 3.0
(18)イソプレングリコール 4.0
(19)POE(10)POP(7)ジメチルエーテル(ランダム共重合体) 0.2
(20)香料 0.6
(21)カチオン化デンプン 0.1
(22)トウガラシチンキ 0.05
(23)メントール 0.1
(24)バニリルブチルエーテル 0.02
(25)カラスムギ抽出液 0.1
(26)フェノキシエタノール 0.4
(27)ベンジルオキシエタノール 0.3
(28)精製水 残余
精製水以外を70℃に温めて、固形分を融解させる。70℃の水を攪拌混合しながら添加する。更に、常温まで冷却する。
配合成分 配合量(質量%)
(1)N-(2-ヒドロキシ-3-ステアロキシプロピル)-N,N-ジメチルアミン 2.5
(2)ステアリルアルコール 6.0
(3)固形パラフィン 0.5
(4)モノオレイン酸グリセリン 0.4
(5)p-トルエンスルホン酸 0.6
(7)香料 0.4
(8)L-アルギニン 0.2
(9)ジメチコン(1000mPa・s) 0.5
(10)アモジメチコン(1000mPa・s) 1.0
(11)ジメチコノール(4000mPa・s) 2.0
(12)イソステアリン酸イソセチル 1.0
(13)グリセリン 5.0
(14)イソプレングリコール 2.0
(15)POE(35)POP(40)ジメチルエーテル(ブロック共重合体)0.3
(16)カチオン化セルロース 0.5
(17)ビワ抽出液 0.2
(18)メチルパラベン 0.3
(19)ベンジルアルコール 0.3
(20)精製水 残余
精製水以外を80℃に温めて、固形分を融解させる。80℃の水を攪拌混合しながら添加する。更に、常温まで冷却する。
配合成分 配合量(質量%)
(1)N-(2-ヒドロキシ-3-ステアロキシプロピル)-N,N-ジメチルアミン 1.0
(2)フェノキシエタノール 0.8
(3)ステアリルアルコール 5.0
(4)ステアリン酸 0.3
(5)2-ナフタレンスルホン酸 0.5
(6)ピロリドンカルボン酸 0.05
(7)香料 0.4
(8)ジメチコン(6mPa・s) 10.0
(9)高重合メチルポリシロキサン(100万mPa・s) 1.0
(10)アモジメチコン(1000mPa・s) 2.0
(11)パルミチン酸オクチル 1.0
(12)POE(5)イソステアリルグリセリルエーテル 0.2
(13)ソルビトール 15.0
(14)ジグリセリン 2.0
(15)ジプロピレングリコール 10.0
(16)高重合ポリエチレングリコール(Mw200万) 0.2
(17)ヒドロキシエチルセルロース 0.2
(18)メントール 0.1
(19)バラ抽出液 0.4
(20)大豆レシチン 0.2
(21)精製水 残余
精製水以外を70℃に温めて、固形分を融解させる。70℃の水を攪拌混合しながら添加する。更に、常温まで冷却する。
Claims (4)
- ヒドロキシエーテルアミン化合物(I)は、下記式(II)にて表されるN-(2-ヒドロキシ-3-ステアロキシプロピル)-N,N-ジメチルアミンである、請求項1に記載の毛髪化粧料。
CH3(CH2)16CH2-O-CH2CH(OH)CH2-N(CH3)2
(II) - 芳香族環骨格を有する有機酸は、サリチル酸類、トルエンスルホン酸、安息香酸類又はナフタレンスルホン酸である、請求項1に記載の毛髪化粧料。
- 芳香族環骨格を有する有機酸は、サリチル酸類、トルエンスルホン酸、安息香酸類又はナフタレンスルホン酸である、請求項2に記載の毛髪化粧料。
Priority Applications (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US13/263,109 US20120070398A1 (en) | 2009-04-10 | 2010-03-31 | Hair Cosmetic |
| CN2010800159696A CN102387777A (zh) | 2009-04-10 | 2010-03-31 | 毛发化妆品 |
| EP10761639A EP2417963A1 (en) | 2009-04-10 | 2010-03-31 | Hair cosmetic |
| BRPI1014898A BRPI1014898A2 (pt) | 2009-04-10 | 2010-03-31 | cosmético capilar. |
| JP2010517214A JPWO2010116940A1 (ja) | 2009-04-10 | 2010-03-31 | 毛髪化粧料 |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2009095423 | 2009-04-10 | ||
| JP2009-095423 | 2009-04-10 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| WO2010116940A1 true WO2010116940A1 (ja) | 2010-10-14 |
Family
ID=42936225
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/JP2010/055969 Ceased WO2010116940A1 (ja) | 2009-04-10 | 2010-03-31 | 毛髪化粧料 |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US20120070398A1 (ja) |
| EP (1) | EP2417963A1 (ja) |
| JP (1) | JPWO2010116940A1 (ja) |
| KR (1) | KR20110135992A (ja) |
| CN (1) | CN102387777A (ja) |
| BR (1) | BRPI1014898A2 (ja) |
| TW (1) | TW201041600A (ja) |
| WO (1) | WO2010116940A1 (ja) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2011105410A1 (ja) * | 2010-02-26 | 2011-09-01 | 株式会社資生堂 | 毛髪形状調整用組成物 |
| JP2017517581A (ja) * | 2014-06-17 | 2017-06-29 | ザ プロクター アンド ギャンブル カンパニー | 毛髪の縮れを軽減するための組成物 |
| JP2021161072A (ja) * | 2020-03-31 | 2021-10-11 | 東邦化学工業株式会社 | 毛髪用組成物 |
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| MX369683B (es) * | 2014-12-05 | 2019-10-02 | Procter & Gamble | Composición para la reducción del encrespado del cabello. |
| EP3226974A1 (en) | 2014-12-05 | 2017-10-11 | The Procter and Gamble Company | Composition for hair frizz reduction |
| US10660835B2 (en) | 2015-04-02 | 2020-05-26 | The Procter And Gamble Company | Method for hair frizz reduction |
| US10632054B2 (en) | 2015-04-02 | 2020-04-28 | The Procter And Gamble Company | Method for hair frizz reduction |
| CN108289814B (zh) | 2015-12-04 | 2022-04-01 | 宝洁公司 | 用于毛发卷曲减少的组合物 |
| WO2017096154A1 (en) | 2015-12-04 | 2017-06-08 | The Procter & Gamble Company | Hair care regimen using compositions comprising moisture control materials |
| KR102463237B1 (ko) * | 2015-12-24 | 2022-11-04 | (주)아모레퍼시픽 | 살리실산 유도체와 그 제조방법 및 이를 함유하는 미백용 화장료 조성물 |
| CN108883038B (zh) | 2016-04-01 | 2022-04-12 | 宝洁公司 | 用于快速干燥毛发的组合物 |
| US10980723B2 (en) | 2017-04-10 | 2021-04-20 | The Procter And Gamble Company | Non-aqueous composition for hair frizz reduction |
| EP4171472A1 (en) | 2020-06-29 | 2023-05-03 | The Procter & Gamble Company | Hair conditioning composition free of fatty alcohol |
| WO2023114680A1 (en) * | 2021-12-16 | 2023-06-22 | The Procter & Gamble Company | Hair conditioning composition |
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| JPH04305516A (ja) * | 1991-04-01 | 1992-10-28 | Shiseido Co Ltd | 毛髪化粧料 |
| JPH0971516A (ja) * | 1995-06-30 | 1997-03-18 | Shiseido Co Ltd | 毛髪化粧料 |
| JP2003081781A (ja) * | 2001-09-14 | 2003-03-19 | Kao Corp | 毛髪化粧料 |
| JP2004002261A (ja) * | 2001-08-06 | 2004-01-08 | Kao Corp | コンディショニング剤 |
| JP2004067534A (ja) * | 2002-08-02 | 2004-03-04 | Kao Corp | 毛髪化粧料 |
| JP2004323495A (ja) * | 2003-04-24 | 2004-11-18 | Toho Chem Ind Co Ltd | 毛髪用組成物 |
| JP2006347997A (ja) * | 2005-06-20 | 2006-12-28 | Kao Corp | 毛髪化粧料 |
| JP2006347996A (ja) * | 2005-06-20 | 2006-12-28 | Kao Corp | 毛髪化粧料 |
| JP2007161605A (ja) * | 2005-12-09 | 2007-06-28 | Shiseido Co Ltd | 毛髪化粧料 |
-
2010
- 2010-03-31 CN CN2010800159696A patent/CN102387777A/zh active Pending
- 2010-03-31 EP EP10761639A patent/EP2417963A1/en not_active Withdrawn
- 2010-03-31 JP JP2010517214A patent/JPWO2010116940A1/ja not_active Withdrawn
- 2010-03-31 BR BRPI1014898A patent/BRPI1014898A2/pt not_active Application Discontinuation
- 2010-03-31 KR KR1020117026741A patent/KR20110135992A/ko not_active Withdrawn
- 2010-03-31 US US13/263,109 patent/US20120070398A1/en not_active Abandoned
- 2010-03-31 WO PCT/JP2010/055969 patent/WO2010116940A1/ja not_active Ceased
- 2010-04-08 TW TW099110925A patent/TW201041600A/zh unknown
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH04305516A (ja) * | 1991-04-01 | 1992-10-28 | Shiseido Co Ltd | 毛髪化粧料 |
| JPH0971516A (ja) * | 1995-06-30 | 1997-03-18 | Shiseido Co Ltd | 毛髪化粧料 |
| JP2004002261A (ja) * | 2001-08-06 | 2004-01-08 | Kao Corp | コンディショニング剤 |
| JP2003081781A (ja) * | 2001-09-14 | 2003-03-19 | Kao Corp | 毛髪化粧料 |
| JP2004067534A (ja) * | 2002-08-02 | 2004-03-04 | Kao Corp | 毛髪化粧料 |
| JP2004323495A (ja) * | 2003-04-24 | 2004-11-18 | Toho Chem Ind Co Ltd | 毛髪用組成物 |
| JP2006347997A (ja) * | 2005-06-20 | 2006-12-28 | Kao Corp | 毛髪化粧料 |
| JP2006347996A (ja) * | 2005-06-20 | 2006-12-28 | Kao Corp | 毛髪化粧料 |
| JP2007161605A (ja) * | 2005-12-09 | 2007-06-28 | Shiseido Co Ltd | 毛髪化粧料 |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2011105410A1 (ja) * | 2010-02-26 | 2011-09-01 | 株式会社資生堂 | 毛髪形状調整用組成物 |
| JP2017517581A (ja) * | 2014-06-17 | 2017-06-29 | ザ プロクター アンド ギャンブル カンパニー | 毛髪の縮れを軽減するための組成物 |
| JP2021161072A (ja) * | 2020-03-31 | 2021-10-11 | 東邦化学工業株式会社 | 毛髪用組成物 |
Also Published As
| Publication number | Publication date |
|---|---|
| EP2417963A1 (en) | 2012-02-15 |
| KR20110135992A (ko) | 2011-12-20 |
| TW201041600A (en) | 2010-12-01 |
| CN102387777A (zh) | 2012-03-21 |
| US20120070398A1 (en) | 2012-03-22 |
| BRPI1014898A2 (pt) | 2016-04-19 |
| JPWO2010116940A1 (ja) | 2012-10-18 |
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