WO2010116941A1 - 毛髪化粧料 - Google Patents
毛髪化粧料 Download PDFInfo
- Publication number
- WO2010116941A1 WO2010116941A1 PCT/JP2010/055970 JP2010055970W WO2010116941A1 WO 2010116941 A1 WO2010116941 A1 WO 2010116941A1 JP 2010055970 W JP2010055970 W JP 2010055970W WO 2010116941 A1 WO2010116941 A1 WO 2010116941A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- group
- hair
- acid
- carbon atoms
- linear
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Ceased
Links
Classifications
-
- 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
- A61K8/365—Hydroxycarboxylic acids; Ketocarboxylic acids
-
- 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
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q5/00—Preparations for care of the hair
-
- 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
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
- An object of the present invention is to provide a 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 hair conditioner, hair rinse, or the like during hair washing. It is an invention.
- the present inventor has studied to solve the above problems, and surprisingly, has found that the problem can be solved by providing a hair cosmetic composition having the following constitution.
- the present invention is an invention that provides a hair cosmetic containing the following components (1) to (5) (hereinafter also referred to as the hair cosmetic of the present invention).
- a tertiary 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 having 6 to 24 carbon atoms
- A is an amide group or an ether group
- R 2 is an alkylene group having 2 to 4 carbon atoms, 2 carbon atoms
- R 3 and R 4 are the same or different and are a hydrogen atom or a linear or branched alkyl group having 1 to 3 carbon atoms. is there.
- Aromatic carboxylates Organic acids that are monobasic acids (5) Water
- aromatic carboxylate is preferably a salt of salicylic acid or a salt of benzoic acid.
- a hair cosmetic that is excellent in hair feel when a conditioner or hair rinse is applied during hair washing.
- R 1 which is a linear or branched alkyl group having 6 to 24 carbon atoms is, for example, hexyl, heptyl, octyl, nonyl, decyl, undecyl, dodecyl, tridecyl, tetradecyl, pentadecyl Group, hexadecyl group, heptadecyl group, octadecyl group, nonadecyl group, icosyl group, heicosyl group, docosyl group, tricosyl group, tetracosyl group, isostearyl group and the like.
- the alkylene group having 2 to 4 carbon atoms that R 2 can take is an ethylene group, trimethylene group or tetramethylene group.
- Examples of the linear or branched hydroxyalkylene group having 2 to 4 carbon atoms include, for example, Hydroxymethylene group, 1-hydroxyethylene group, 2-hydroxyethylene group, 1-hydroxytrimethylene group, 2-hydroxytrimethylene group, 3-hydroxytrimethylene group, 1-hydroxytetramethylene group, 2-hydroxytetramethylene group 3-hydroxytetramethylene group, 4-hydroxytetramethylene group, 1-hydroxypentamethylene group, 2-hydroxypentamethylene group, 3-hydroxypentamethylene group, 4-hydroxypentamethylene group, 5-hydroxypentamethylene group, 1-hydroxyhexamethylene group, 2 -Hydroxyhexamethylene group, 3-hydroxyhexamethylene group, 4-hydroxyhexamethylene group, 5-hydroxyhexamethylene group, 6-hydroxyhexamethylene group, and the like.
- R 3 and R 4 are the same or different and are a hydrogen atom
- the tertiary amine compound (I) particularly preferred in the present invention is that R 1 is a stearyl group (octadecyl group), A is an ether group or an amide group, and R 2 is —CH 2 —CH (OH) —.
- the tertiary 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 tertiary amine compound (I) in the hair cosmetic composition of the present invention is 0.01 to 10 mass%, preferably 0.1 to 5 mass% of the cosmetic composition.
- 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. Yes, when 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. If the blending amount is less than 0.1% by mass, the improvement of the feel 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 due to blending of higher fatty acid and / or higher alcohol is not recognized. When it exceeds the mass%, the effect of improving the feel at the time of application commensurate with a large amount of compounding is substantially not recognized.
- Organic acid salt having an aromatic ring skeleton examples of the aromatic carboxylate that can be blended in the hair cosmetic composition of the present invention include, for example, salts of salicylic acids (eg, salicylate, 3-methylsalicylate, 4 -Methyl salicylate, 5-methyl salicylate, etc.), benzoic acid salts (benzoate, 2-methylbenzoate, 3-methylbenzoate, 4-methylbenzoate, etc.), and these One or more aromatic carboxylates can be used as necessary. Of these, salicylate is preferred.
- the salt referred to here means all pharmaceutically acceptable salts such as sodium salt, potassium salt, calcium salt, triethanolamine salt and the like.
- the blending amount of the aromatic organic acid salt 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 more than the above-mentioned tertiary amine compound (I). 1 mole.
- 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, and the odor due to the excessive presence of the aromatic organic acid salt There is a tendency to be irritated.
- Organic acids that are monobasic acids include lactic acid, glycolic acid, pyrrolidone carboxylic acid, acetic acid, butyric acid, and glutamic acid.
- an organic acid which is a monobasic acid
- a monoalkyl type pseudo-cationic surfactant is formed, and the above-mentioned aromatic organic acid salt has a lamella structure. It enters the gap of the rinse gel (palisade layer).
- the amount of the organic acid, which is a monobasic acid for forming such a state, to the hair cosmetic composition of the present invention is 0.1 mol or more, preferably 0, relative to the tertiary amine compound (I). .5 to 1 mole.
- the pH of the system is preferably in the vicinity of the pKa of the organic acid of the monobasic acid used.
- 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 may be blended as the balance of the blending amount (mass%) of the above essential components and the blending amount (mass%) of other components described later, taking into consideration the dosage form and form of the hair cosmetic. Typical.
- 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. 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 tauric acid, N-acyl glutamate salt
- amphoteric surfactants such as alkylamide betaines and imidazolinium betaines
- nonionic surfactants such as fatty acid alkanolamines and the like.
- oils other than the above 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; Agent; ultraviolet absorber; antioxidant; antiseptic; powder component; blood circulation promoter, local stimulant, hair follicle activator, antiandrogen hormone agent, antiseborrheic agent, keratolytic agent, bactericidal agent, anti-inflammatory agent, amino acid , 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.
- the blending amount is mass% unless otherwise specified.
- Evaluation methods used for the hair cosmetic of the present invention are shown below.
- (1) Use feeling test The actual use test regarding the feeling at the time of application was conducted by six female panels. Specifically, a test sample (hair rinse) is applied to the wet hair immediately after shampooing by hand, and the coating feel at that time is (1) the growth of the preparation on the hair, and (2) the suppleness of the hair. The following four criteria were evaluated: (3) smoothness of hair, and (4) moist feeling of hair.
- 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 the 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.
- stearoxyhydroxypropylamine is N- (2-hydroxy-3-stearoxypropyl) -N, N-dimethylamine (II)
- stearoxypropyldimethylamine is N-stearoxypropyl-N, N-dimethylamine (III)
- stearamidopropyldimethylamine mean N-stearamidopropyl-N, N-dimethylamine (IV).
- Comparative Example 1 when the compounding amount of stearoxyhydroxypropylamine (tertiary amine compound (I)) is small, even when the compounding amount of other essential components is within the regulation of the present invention, the touch at the time of application was found to be bad in all items.
- Comparative Example 2 it was found that even when the compounding amount of stearoxyhydroxypropylamine was larger than the specified range of the present invention, the feel at the time of application was not excellent.
- Comparative Examples 3 and 4 even when the amount of stearyl alcohol (higher alcohol) is too small (Comparative Example 3) or too much (Comparative Example 4), the touch feeling tends to be inferior. found.
- Comparative Example 5 it was found that when no organic acid was blended, the feel during application was inferior. According to Comparative Example 6, even when salicylic acid (an organic acid having an aromatic ring) was blended, the feel during coating was the same. It became clear that it did not reach the invention. Further, Comparative Examples 7 to 10 reveal that even when an organic acid having a basic acid number of 2 or more is blended, the feel at the time of application is not as good as that of the present invention in which a monobasic organic acid is blended. .
- Hair conditioner Compounding component amount (% by mass) (1) N- (2-hydroxy-3-stearoxypropyl) -N, N-dimethylamine 1.5 (2) Lactic acid 0.6 (3) Sodium salicylate 0.3 (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
- ⁇ 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) Sodium benzoate 0.6 (7) Fragrance 0.4 (8) Glycolic acid 0.5 (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 0.3 (20) Purified water residue
- ⁇ 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.
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Birds (AREA)
- Epidemiology (AREA)
- Emergency Medicine (AREA)
- Dermatology (AREA)
- Cosmetics (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
Description
(1)下記式(I)にて表される第三級アミン化合物を、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)芳香族カルボン酸塩
(4)一塩基酸である有機酸
(5)水
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、イソステアリル基等が挙げられる。また、R2がとり得る、炭素数2~4のアルキレン基は、エチレン基、トリメチレン基又はテトラメチレン基であり、炭素数2~4の直鎖若しくは分岐鎖のヒドロキシアルキレン基としては、例えば、ヒドロキシメチレン基、1-ヒドロキシエチレン基、2-ヒドロキシエチレン基、1-ヒドロキシトリメチレン基、2-ヒドロキシトリメチレン基、3-ヒドロキシトリメチレン基、1-ヒドロキシテトラメチレン基、2-ヒドロキシテトラメチレン基、3-ヒドロキシテトラメチレン基、4-ヒドロキシテトラメチレン基、1-ヒドロキシペンタメチレン基、2-ヒドロキシペンタメチレン基、3-ヒドロキシペンタメチレン基、4-ヒドロキシペンタメチレン基、5-ヒドロキシペンタメチレン基、1-ヒドロキシヘキサメチレン基、2-ヒドロキシヘキサメチレン基、3-ヒドロキシヘキサメチレン基、4-ヒドロキシヘキサメチレン基、5-ヒドロキシヘキサメチレン基、6-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の直鎖若しくは分岐鎖のアルキル基である。
CH3(CH2)16CH2-O-CH2CH(OH)CH2-N(CH3)2 (II)
CH3(CH2)16CH2-O-CH2CH2CH2-N(CH3)2 (III)
CH3(CH2)16CH2-CONH-CH2CH2CH2-N(CH3)2 (IV)
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、芳香族カルボン酸塩としては、例えば、サリチル酸類の塩(例えば、サリチル酸塩、3-メチルサリチル酸塩、4-メチルサリチル酸塩、5-メチルサリチル酸塩等)、安息香酸類の塩(安息香酸塩、2-メチル安息香酸塩、3-メチル安息香酸塩、4-メチル安息香酸塩等)が挙げられ、これらの芳香族カルボン酸塩を必要に応じて1種又は2種以上用いることができる。これらの中でも、サリチル酸塩が好適である。なお、ここにいう塩とは、製薬学上許容される全ての塩を意味するものであり、例えば、ナトリウム塩、カリウム塩、カルシウム塩、トリエタノールアミン塩、等が挙げられる。
一塩基酸の有機酸としては、例えば、乳酸、グリコール酸、ピロリドンカルボン酸、酢酸、酪酸、グルタミン酸等が挙げられる。一塩基酸である有機酸を本発明の毛髪化粧料に添加することで、モノアルキル型の疑似カチオン界面活性剤が形成され、さらに、上記の芳香族有機酸塩が、形成されたラメラ構造のリンスゲルの隙間(パリセード層)に入り込む。このような状態を形成するための一塩基酸である有機酸の本発明の毛髪化粧料への配合量は、第三級アミン化合物(I)に対して0.1モル以上、好適には0.5~1モルである。また、系のpHは、使用する一塩基酸の有機酸のpKa付近であることが好適である。
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、後述する他の成分の配合量(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。
(1)使用感触試験
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、以下において、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、ステアロキシプロピルジメチルアミンはN-ステアロキシプロピル-N,N-ジメチルアミン(III)を、ステアラミドプロピルジメチルアミンはN-ステアラミドプロピル-N,N-ジメチルアミン(IV)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)乳酸 0.6
(3)サリチル酸ナトリウム 0.3
(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)安息香酸ナトリウム 0.6
(7)香料 0.4
(8)グリコール酸 0.5
(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-ステアロキシプロピル-N,N-ジメチルアミン 1.0
(2)乳酸 0.5
(3)ステアリルアルコール 5.0
(4)ステアリン酸 0.3
(5)サリチル酸ナトリウム 0.4
(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 (2)
- 前記芳香族カルボン酸塩が、サリチル酸類の塩、又は、安息香酸類の塩、である、請求項1に記載の毛髪化粧料。
Priority Applications (6)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2010517215A JPWO2010116941A1 (ja) | 2009-04-10 | 2010-03-31 | 毛髪化粧料 |
| CN2010800159709A CN102387776A (zh) | 2009-04-10 | 2010-03-31 | 毛发化妆品 |
| US13/263,126 US20120093751A1 (en) | 2009-04-10 | 2010-03-31 | Hair Cosmetic |
| BRPI1014159A BRPI1014159A2 (pt) | 2009-04-10 | 2010-03-31 | cosmético capilar |
| RU2011141742/15A RU2011141742A (ru) | 2009-04-10 | 2010-03-31 | Косметическое средство для волос |
| EP10761640A EP2417961A1 (en) | 2009-04-10 | 2010-03-31 | Hair cosmetic |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2009095430 | 2009-04-10 | ||
| JP2009-095430 | 2009-04-10 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| WO2010116941A1 true WO2010116941A1 (ja) | 2010-10-14 |
Family
ID=42936226
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/JP2010/055970 Ceased WO2010116941A1 (ja) | 2009-04-10 | 2010-03-31 | 毛髪化粧料 |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US20120093751A1 (ja) |
| EP (1) | EP2417961A1 (ja) |
| JP (1) | JPWO2010116941A1 (ja) |
| KR (1) | KR20120022901A (ja) |
| CN (1) | CN102387776A (ja) |
| BR (1) | BRPI1014159A2 (ja) |
| RU (1) | RU2011141742A (ja) |
| TW (1) | TW201043254A (ja) |
| WO (1) | WO2010116941A1 (ja) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20140371332A1 (en) * | 2012-02-13 | 2014-12-18 | Kao Corporation | Method for producing vesicle composition |
| JP2017511346A (ja) * | 2014-04-23 | 2017-04-20 | ザ プロクター アンド ギャンブル カンパニー | 皮膚を水和させるための美容組成物 |
| JP2017518380A (ja) * | 2014-06-17 | 2017-07-06 | 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 |
| JP2024061232A (ja) * | 2022-10-21 | 2024-05-07 | 東洋ビューティ株式会社 | ヘアコンディショニング組成物 |
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US10111815B2 (en) | 2014-06-17 | 2018-10-30 | The Procter And Gamble Company | Composition for hair frizz reduction |
| EP3226974A1 (en) * | 2014-12-05 | 2017-10-11 | The Procter and Gamble Company | Composition for hair frizz reduction |
| MX369683B (es) | 2014-12-05 | 2019-10-02 | Procter & Gamble | Composición para la reducción del encrespado del cabello. |
| 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 |
| WO2017096154A1 (en) | 2015-12-04 | 2017-06-08 | The Procter & Gamble Company | Hair care regimen using compositions comprising moisture control materials |
| CN108289814B (zh) | 2015-12-04 | 2022-04-01 | 宝洁公司 | 用于毛发卷曲减少的组合物 |
| 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 |
| US12083206B2 (en) | 2020-05-29 | 2024-09-10 | L'oreal | Hair treatment compositions |
| FR3112479B1 (fr) * | 2020-07-16 | 2023-04-21 | Oreal | Compositions de traitement des cheveux |
Citations (9)
| 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 |
| 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 JP JP2010517215A patent/JPWO2010116941A1/ja not_active Withdrawn
- 2010-03-31 WO PCT/JP2010/055970 patent/WO2010116941A1/ja not_active Ceased
- 2010-03-31 CN CN2010800159709A patent/CN102387776A/zh active Pending
- 2010-03-31 BR BRPI1014159A patent/BRPI1014159A2/pt not_active Application Discontinuation
- 2010-03-31 RU RU2011141742/15A patent/RU2011141742A/ru unknown
- 2010-03-31 US US13/263,126 patent/US20120093751A1/en not_active Abandoned
- 2010-03-31 KR KR1020117026743A patent/KR20120022901A/ko not_active Withdrawn
- 2010-03-31 EP EP10761640A patent/EP2417961A1/en not_active Withdrawn
- 2010-04-08 TW TW099110924A patent/TW201043254A/zh unknown
Patent Citations (9)
| 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 (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20140371332A1 (en) * | 2012-02-13 | 2014-12-18 | Kao Corporation | Method for producing vesicle composition |
| JP2017511346A (ja) * | 2014-04-23 | 2017-04-20 | ザ プロクター アンド ギャンブル カンパニー | 皮膚を水和させるための美容組成物 |
| JP2017518380A (ja) * | 2014-06-17 | 2017-07-06 | 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 |
| JP2024061232A (ja) * | 2022-10-21 | 2024-05-07 | 東洋ビューティ株式会社 | ヘアコンディショニング組成物 |
| JP7618258B2 (ja) | 2022-10-21 | 2025-01-21 | 東洋ビューティ株式会社 | ヘアコンディショニング組成物 |
Also Published As
| Publication number | Publication date |
|---|---|
| KR20120022901A (ko) | 2012-03-12 |
| CN102387776A (zh) | 2012-03-21 |
| BRPI1014159A2 (pt) | 2016-04-26 |
| EP2417961A1 (en) | 2012-02-15 |
| TW201043254A (en) | 2010-12-16 |
| RU2011141742A (ru) | 2013-05-20 |
| JPWO2010116941A1 (ja) | 2012-10-18 |
| US20120093751A1 (en) | 2012-04-19 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| WO2010116941A1 (ja) | 毛髪化粧料 | |
| JPWO2010116940A1 (ja) | 毛髪化粧料 | |
| EP2387987B1 (en) | Hair cosmetic | |
| JP5655127B2 (ja) | ヘアコンディショナー組成物 | |
| US8293220B2 (en) | Hair cosmetic | |
| BR112020004478A2 (pt) | composição contendo composto de amônio quaternário, especialmente para produzir formulações de cuidados e limpeza | |
| BRPI1100869A2 (pt) | composições compreendendo compostos de amÈnio quaternário e carbonatos orgánicos | |
| CN107683163B (zh) | 包含长链酯的化妆品组合物和用于毛发处理的用途 | |
| TW200936174A (en) | Hair cosmetic composition | |
| KR101948582B1 (ko) | 컨디셔닝 제제 및 컨디셔닝용 조성물 | |
| JP5952590B2 (ja) | 毛髪用組成物 | |
| JP2010241773A (ja) | 毛髪化粧料 | |
| JP5172214B2 (ja) | 毛髪化粧料 | |
| JP4772361B2 (ja) | 毛髪化粧料 | |
| JP5946724B2 (ja) | 毛髪化粧料 | |
| JP2017193515A (ja) | 速乾性毛髪化粧料及びそれを用いた毛髪に速乾性を付与する方法 | |
| US20120093758A1 (en) | Hair Cosmetic | |
| JP2012102065A (ja) | 毛髪化粧料の使用方法、その毛髪化粧料 | |
| JP2010013404A (ja) | 毛髪化粧料 | |
| JP2010241774A (ja) | 毛髪化粧料 | |
| JP2010013406A (ja) | 毛髪化粧料 | |
| JP2010241775A (ja) | 毛髪化粧料 | |
| HK1164117A (en) | Hair cosmetic | |
| JPWO2019065576A1 (ja) | 毛髪化粧料 | |
| HK1164116A (en) | Hair cosmetic |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| WWE | Wipo information: entry into national phase |
Ref document number: 201080015970.9 Country of ref document: CN |
|
| WWE | Wipo information: entry into national phase |
Ref document number: 2010517215 Country of ref document: JP |
|
| 121 | Ep: the epo has been informed by wipo that ep was designated in this application |
Ref document number: 10761640 Country of ref document: EP Kind code of ref document: A1 |
|
| DPE1 | Request for preliminary examination filed after expiration of 19th month from priority date (pct application filed from 20040101) | ||
| NENP | Non-entry into the national phase |
Ref country code: DE |
|
| WWE | Wipo information: entry into national phase |
Ref document number: 2010761640 Country of ref document: EP |
|
| WWE | Wipo information: entry into national phase |
Ref document number: 8499/DELNP/2011 Country of ref document: IN |
|
| ENP | Entry into the national phase |
Ref document number: 20117026743 Country of ref document: KR Kind code of ref document: A |
|
| ENP | Entry into the national phase |
Ref document number: 2011141742 Country of ref document: RU Kind code of ref document: A |
|
| WWE | Wipo information: entry into national phase |
Ref document number: 13263126 Country of ref document: US |
|
| REG | Reference to national code |
Ref country code: BR Ref legal event code: B01A Ref document number: PI1014159 Country of ref document: BR |
|
| ENP | Entry into the national phase |
Ref document number: PI1014159 Country of ref document: BR Kind code of ref document: A2 Effective date: 20111010 |