WO2001074305A1 - Compositions cosmetiques - Google Patents
Compositions cosmetiques Download PDFInfo
- Publication number
- WO2001074305A1 WO2001074305A1 PCT/JP2001/002703 JP0102703W WO0174305A1 WO 2001074305 A1 WO2001074305 A1 WO 2001074305A1 JP 0102703 W JP0102703 W JP 0102703W WO 0174305 A1 WO0174305 A1 WO 0174305A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- arginine
- hair
- mono
- powder
- skin
- Prior art date
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
- A61K8/40—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
- A61K8/44—Aminocarboxylic acids or derivatives thereof, e.g. aminocarboxylic acids containing sulfur; Salts; Esters or N-acylated derivatives 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
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/84—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions otherwise than those involving only carbon-carbon unsaturated bonds
- A61K8/89—Polysiloxanes
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q19/00—Preparations for care of the skin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q19/00—Preparations for care of the skin
- A61Q19/02—Preparations for care of the skin for chemically bleaching or whitening the skin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q19/00—Preparations for care of the skin
- A61Q19/10—Washing or bathing preparations
-
- 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
- A61Q5/02—Preparations for cleaning 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 a cosmetic composition. More specifically, the present invention relates to a cosmetic composition that gives gloss to hair and skin, or that gives less slimy feeling to the skin and scalp during rinsing and less irritability after drying. Background art
- an anionic surfactant or an amphoteric surfactant is mainly used as a cleaning component.
- these cleaning ingredients have disadvantages, such as lack of luster when used on fine hair, and the absence of glue on hair.
- the hair is treated with a conditioning agent consisting of a cation surfactant and an oil in order to improve the finish of the hair.However, since the conditioning agent removes a large portion of the hair, the hair after drying is glossy. However, there is a problem that it is difficult to effectively provide the same.
- various oils, polyols, various polymers, and the like are blended to keep the skin radiant and shiny, but their effects have not always been satisfied.
- cosmetic silicone compounds are often added to shampoos, rinses or treatments to improve these problems.
- the silicone compound was washed away together with the surfactant, and the effect could not be sufficiently exhibited.
- the above-mentioned silicone compound is blended in the rinse or the treatment, it flows during rinsing together with the oil agent and effectively imparts gloss to the hair after drying. There was a problem that it was difficult.
- Cosmetic silicone is included in skin cosmetics to improve spreadability during application and smoothness and luster during use.How to improve skin luster after use Satisfaction was not always obtained with the addition of silicone for cosmetics alone.
- the amphoteric surfactant used in the detergent composition is useful for improving the foaming and detergency of the anionic surfactant and for giving a mild feeling of use.
- the drawback is that the rinsing property at the time of rinsing is poor, that the skin or scalp becomes slimy, and that a dry feeling remains after drying. there were.
- various extender pigments may be blended.However, the extender pigment is washed away during cleaning, and many parts are washed away. It was difficult to effectively reduce the feeling of sliminess. Disclosure of the invention
- An object of the present invention is to provide a cosmetic composition. More specifically, it is an object of the present invention to provide a cosmetic composition that gives a shine and gloss to hair and skin. Another object of the present invention is to provide a detergent composition having a reduced slimy feeling upon rinsing when used for washing and a reduced feeling of shine after drying.
- the present invention provides (A) one or more kinds selected from mono- ⁇ -long-chain acetyl arginine and / or a powder which has been surface-treated with mono- ⁇ -long-chain acetyl arginine.
- An object of the present invention is to provide a cosmetic composition containing one or more powders, (i) a silicone compound for cosmetics, and (ii) an amphoteric surfactant.
- the above cosmetic composition for application to skin or hair.
- composition containing at least one powder selected from the group consisting of (i) and a silicone compound for cosmetics is characterized in that when applied to the skin or the hair, the hair or skin is given a lustrous and lustrous finish.
- composition (Alpha) mono - ⁇ ⁇ - 1 or more and / or mono selected from long chain ⁇ sill arginine - New "- flour was surface-treated with a long chain ⁇ sill arginine
- the composition containing one or more powders selected from the body and ( ⁇ ) an amphoteric surfactant has a reduced slimy feeling when rinsed when used for washing, and a reduced irritability after drying. ing.
- the present invention provides a method for imparting a glue and / or gloss to hair or skin, comprising: ( ⁇ ) one or more mono- / ⁇ -long chain acetyl arginines and / or a mono- ⁇ A method comprising the step of applying to the hair or skin a composition containing one or more powders selected from powders that have been surface-treated with long-chain acetyl arginine, and ( ⁇ ) a cosmetic silicone compound; And a method for cleaning hair or skin, comprising: Bruno - New alpha - 1 or more and / or mono selected from long chain ⁇ sill arginine - ⁇ ⁇ - 1 or more and a powder selected from powder was surface-treated with a long chain ⁇ sill arginine (beta)
- the present invention provides a method including a step of performing washing using a composition containing an amphoteric surfactant.
- the present invention relates to ( ⁇ ) one or more kinds selected from mono- ⁇ long chain acetyl arginine and ⁇ or mono- ⁇ ⁇ -long chain arginine for the production of the above cosmetic composition.
- the use of one or more kinds of powders selected from surface-treated powders, and the use of ( ⁇ ) a cosmetic silicone compound and / or an amphoteric surfactant for the production of the above-mentioned cosmetic composition are described.
- mono-- ⁇ - acyl arginine which can be used in the present invention is obtained by converting arginine with a long-chain fatty acid salt or a ride under alkaline conditions ( ⁇ 12). Or with a hydrophilic solvent, or by heating and dehydrating arginine and a salt of a fatty acid at a temperature of 100-250 ° C. as described in JP-A-49-1513. it can. Further, as disclosed in JP-A-11-228527, arginine and a long-chain fatty acid halide are mixed with a lower alcohol // and / or a mixed solvent of polyhydric alcohol and water to make the mixture alkaline. After reacting in the presence (pH 10-13), dissolve it sufficiently as an acidic or basic aqueous solution, and then adjust the pH to 5 to 7 to obtain crystals of mono- ⁇ - acylarginine. Can be.
- mono - New alpha - ⁇ Sil arginine are those having a linear or fatty Ashiru group, saturated or unsaturated branched 8 to 28 carbon atoms
- the arginine portion of mono-acyl arginine may be any of D-form, L-form and DL-form.
- two or more mono- ⁇ -acyl arginines may be used in combination.
- the surface treatment method of the powder that has been surface-treated with mono- ⁇ - acyl arginine (hereinafter sometimes referred to as “treated powder” in the present specification) that can be used in the present invention is not particularly limited.
- either wet processing or dry processing may be used.
- a wet method it can be obtained by dissolving in a solution containing a strong acid or a strong organic solvent and then neutralizing the solution.
- dry processes powder and mono coated from rotational speed several thousand tens of thousands pm of mixed-grinder - New alpha - was charged with ⁇ sill arginine, mechanically mono -v «- Ashiru It can be obtained by coating the powder with arginine.
- the particle size of the processed powder is not particularly limited, and can be appropriately selected according to the type of the processed powder.
- the type of raw material powder used for the treated powder that can be used in the present invention is not particularly limited.
- Pigment, chlorophyll,? -Carotene and the like talc, mica, sericite, boron nitride, nylon powder, polyethylene powder, red iron oxide, iron titanate, and fine particle titanium oxide are preferable, and talc, mica, sericite, and boron nitride are most preferable.
- Amount of ⁇ sill arginine in that it can perform the waste name 1, uniform surface treatment, 0 relative to the weight of the powder to be processed 0 1 It is preferably used in a proportion of up to 30% by weight, more preferably 0.1 to 15% by weight, even more preferably 0.5 to 5% by weight.
- the type of the silicone compound for cosmetics that can be used in the present invention is not particularly limited.
- examples include silicone resin, methylphenylpolysiloxane, methylpolysiloxane, octamethylcyclotetrasiloxane, dimethylsiloxane-methyl (polyoxyethylene) siloxane copolymer, decamethylcyclopentanesiloxane, Dimethylsiloxane methyl (polyoxyethylene 'polyoxypropylene) siloxane copolymer, methylhydrogenpolysiloxane, dodecamethylcyclohexasiloxane, methylpolycyclosiloxane, dimethylsiloxane / methylstearylsiloxane copolymer, methylpolysiloxane Emulsion, oxymethyltrisiloxane, cyclic silicone resin, highly polymerized methylpolysiloxane, tetradecamethylhexasi
- the amount of the cosmetic silicone used in the present invention can be appropriately determined according to the desired performance of the cosmetic composition, and is not particularly limited. For example, it is usually 0.01 to 30% by weight, preferably 0.1 to 10% by weight, and more preferably 0.2 to 5% by weight, based on the total amount of the cosmetic composition. . Two or more cosmetic silicones may be used in combination.
- amphoteric surfactant that can be used in the present invention is not particularly limited.
- carbo-bein-in amphoteric surfactant amide-bein-in amphoteric surfactant, sulfo-bein-in amphoteric surfactant, hydroxysulfo-bein-in amphoteric surfactant, amid-sulfobein-in surfactant
- Amphoteric surfactants such as amphoteric surfactants, phospho-bein-type amphoteric surfactants, and imidazoline-type amphoteric surfactants.
- the amount of the amphoteric surfactant used in the present invention can be appropriately determined depending on the desired performance of the cosmetic composition, and is not particularly limited. For example, it is usually 0.01 to 30% by weight, preferably 0.1 to 15% by weight, and more preferably 0.2 to 10% by weight, based on the total amount of the cosmetic composition. Two or more surfactants may be used in combination.
- the use of the cosmetic composition of the present invention is not particularly limited, it can be preferably used as a cosmetic composition for skin or hair.
- the cosmetic composition can
- additives usually used can be added to the cosmetic composition of the present invention as long as the effects of the present invention are not impaired.
- Such additives are used in the cosmetics field. It is widely used and can be appropriately selected by those skilled in the art. Examples include surfactants such as anionic surfactants, cationic surfactants, nonionic surfactants, class I, vegetable oils, animal oils and fats, natural oils and fats derivatives, mineral oils and fats, lower and higher fatty acid esters,
- Synthetic fats and oils such as N-acylglutamic acid ester, polymeric substances, alcohols, polyhydric alcohols, extracts, amino acids, nucleic acids, vitamins, hydrolyzed proteins and their derivatives, glycerol oleate, enzymes, anti-inflammatory agents, sterilization
- Raw material standards for cosmetics, preservatives, antioxidants, ultraviolet absorbers, chelating agents, antiperspirants, oxidation dyes, pH adjusters, pearling agents, wetting agents, etc. standard specifications for cosmetic ingredients, quasi-drugs Standards, Japanese Pharmacopoeia, raw materials described in the compendium of food additives, and the like. These additives may be used in combination of two or more.
- a shampoo having the composition shown in Table 1 (indicated by weight%, total amount 100%) was prepared by a conventional method, and these shampoos were applied to a hair bundle washed with a 1% aqueous solution of sodium lauryl ether sulfate, thoroughly washed with water, and dried. Sensory evaluation was performed on (a) gloss of hair and (b) beam of hair. The evaluation was a relative evaluation using Comparative Example 1 in Table 1 as a standard product. The average value was calculated according to the following criteria. The case of 5-4.4 was evaluated as good ( ⁇ ), the case of 2.5-3.4 as normal ( ⁇ ;), and the case of 2.4 or less as poor (X). Table 1 shows the evaluation results. ⁇ Evaluation criteria>
- a shampoo was prepared according to a conventional method using the following formulation.
- the shampoo thus prepared moistened the hair after washing, and was excellent in the gloss and shine of the hair for the purpose of the present invention.
- a hair treatment was prepared according to the following formulation by a conventional method.
- PCA soda made by Ajinomoto
- a hair rinse was prepared according to a standard method using the following formulation.
- the prepared rinsing spreads well when applied to hair, and has excellent stickiness after being applied to hair and dried.
- Example 4 A shampoo having the composition shown in Table 4 (indicated by weight%, total amount 100%) was prepared by a conventional method, and these shampoos were washed with a 1% aqueous solution of sodium lauryl ether sulfate, and then thoroughly washed with water. Sensory evaluation was performed on a) the ease of rinsing and (b) the stickiness after drying. Table 4 shows the evaluation results. The evaluation was performed according to the following criteria.
- Palmitoyl arginine 1 1.0 1.0 1 1 1 Stearoyl arginine 0.5 0.5
- the cosmetics composition which gives a gloss
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- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Dermatology (AREA)
- Birds (AREA)
- Epidemiology (AREA)
- Cosmetics (AREA)
Description
Claims
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP01917658A EP1269969A4 (en) | 2000-04-03 | 2001-03-30 | COSMETIC COMPOSITIONS |
US10/239,865 US20040052747A1 (en) | 2000-04-03 | 2001-03-30 | Cosmetic compositions |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2000-100322 | 2000-04-03 | ||
JP2000100322 | 2000-04-03 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2001074305A1 true WO2001074305A1 (fr) | 2001-10-11 |
Family
ID=18614545
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/JP2001/002703 WO2001074305A1 (fr) | 2000-04-03 | 2001-03-30 | Compositions cosmetiques |
Country Status (4)
Country | Link |
---|---|
US (1) | US20040052747A1 (ja) |
EP (1) | EP1269969A4 (ja) |
KR (1) | KR20030005257A (ja) |
WO (1) | WO2001074305A1 (ja) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1264591A2 (en) * | 2001-06-06 | 2002-12-11 | Ajinomoto Co., Inc. | Cosmetic composition |
EP1264590A2 (en) * | 2001-06-06 | 2002-12-11 | Ajinomoto Co., Inc. | Cosmetic composition |
FR2835431A1 (fr) * | 2002-02-05 | 2003-08-08 | Ajinomoto Kk | COMPOSITION COSMETIQUE CONTENANT UNE Nx,Ng-DIACYLARGININE |
Families Citing this family (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP4475970B2 (ja) * | 2004-01-29 | 2010-06-09 | 三好化成株式会社 | 化粧料 |
DE102009034115A1 (de) * | 2009-07-20 | 2011-01-27 | Beiersdorf Ag | Kosmetische Zubereitung mit einem Gehalt an Acylarginaten |
KR101593053B1 (ko) | 2014-08-26 | 2016-02-11 | 국방과학연구소 | 압력변화 완화용 내장형 멤브레인 장치 |
CN105037216A (zh) * | 2015-08-05 | 2015-11-11 | 上海应用技术学院 | 一种月桂酰精氨酸盐酸盐的制备方法 |
CN107286059A (zh) * | 2017-05-19 | 2017-10-24 | 武汉桀升生物科技有限公司 | 一种月桂酰精氨酸乙酯盐酸盐的制备方法 |
CN108101812B (zh) * | 2018-01-02 | 2020-12-25 | 成都傲飞生物化学品有限责任公司 | 一种月桂酰精氨酸乙酯盐酸盐的生产纯化工艺 |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5931706A (ja) * | 1982-08-17 | 1984-02-20 | Lion Corp | 化粧料組成物 |
JPH07277937A (ja) * | 1994-04-01 | 1995-10-24 | Ajinomoto Co Inc | 化粧用粉体およびそれを含有する化粧料 |
JPH08337519A (ja) * | 1995-06-13 | 1996-12-24 | Ajinomoto Co Inc | 化粧料 |
JPH11228348A (ja) * | 1998-02-09 | 1999-08-24 | Ajinomoto Co Inc | 化粧料組成物 |
JPH11228527A (ja) * | 1998-02-10 | 1999-08-24 | Ajinomoto Co Inc | 長鎖アシルアルギニン結晶及びその製造方法 |
Family Cites Families (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3740421A (en) * | 1966-09-19 | 1973-06-19 | Basf Wyandotte Corp | Polyoxyethylene-polyoxypropylene aqueous gels |
JPS5939819A (ja) * | 1982-08-31 | 1984-03-05 | Lion Corp | ヘア−リンス剤組成物 |
JPS59110609A (ja) * | 1982-12-15 | 1984-06-26 | Lion Corp | 毛髪化粧料 |
JPH03778A (ja) * | 1990-01-03 | 1991-01-07 | Kenji Ichikawa | 抗菌性塗料 |
FR2676921B1 (fr) * | 1991-05-27 | 1995-04-14 | Oreal | Emulsion stable du type huile-dans-eau a base d'huile de silicone et son utilisation en cosmetique et en dermatologie. |
FR2677995B1 (fr) * | 1991-06-21 | 1994-07-22 | Oreal | Composition de lavage et/ou de conditionnement des matieres keratiniques, contenant une silicone et un polymere amphotere derive de diallyldialkylammonium et d'un monomere anionique. |
JP2990624B2 (ja) * | 1991-10-21 | 1999-12-13 | 味の素株式会社 | 油溶性n−長鎖アシル中性アミノ酸エステル及びそれらを含む香粧品及び外用医薬基剤 |
US5747017A (en) * | 1995-05-15 | 1998-05-05 | Lip-Ink International | Lip cosmetic |
US7297717B2 (en) * | 2000-04-27 | 2007-11-20 | Kao Corporation | Emulsion cosmetic |
-
2001
- 2001-03-30 US US10/239,865 patent/US20040052747A1/en not_active Abandoned
- 2001-03-30 EP EP01917658A patent/EP1269969A4/en not_active Withdrawn
- 2001-03-30 KR KR1020027013190A patent/KR20030005257A/ko active IP Right Grant
- 2001-03-30 WO PCT/JP2001/002703 patent/WO2001074305A1/ja active Application Filing
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5931706A (ja) * | 1982-08-17 | 1984-02-20 | Lion Corp | 化粧料組成物 |
JPH07277937A (ja) * | 1994-04-01 | 1995-10-24 | Ajinomoto Co Inc | 化粧用粉体およびそれを含有する化粧料 |
JPH08337519A (ja) * | 1995-06-13 | 1996-12-24 | Ajinomoto Co Inc | 化粧料 |
JPH11228348A (ja) * | 1998-02-09 | 1999-08-24 | Ajinomoto Co Inc | 化粧料組成物 |
JPH11228527A (ja) * | 1998-02-10 | 1999-08-24 | Ajinomoto Co Inc | 長鎖アシルアルギニン結晶及びその製造方法 |
Non-Patent Citations (1)
Title |
---|
See also references of EP1269969A4 * |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1264591A2 (en) * | 2001-06-06 | 2002-12-11 | Ajinomoto Co., Inc. | Cosmetic composition |
EP1264590A2 (en) * | 2001-06-06 | 2002-12-11 | Ajinomoto Co., Inc. | Cosmetic composition |
EP1264591A3 (en) * | 2001-06-06 | 2003-07-02 | Ajinomoto Co., Inc. | Cosmetic composition |
EP1264590A3 (en) * | 2001-06-06 | 2003-07-02 | Ajinomoto Co., Inc. | Cosmetic composition |
US6974582B2 (en) | 2001-06-06 | 2005-12-13 | Ajinomoto Co., Inc. | Cosmetic composition |
KR100889245B1 (ko) * | 2001-06-06 | 2009-03-19 | 아지노모토 가부시키가이샤 | 신규 화장품 조성물 |
FR2835431A1 (fr) * | 2002-02-05 | 2003-08-08 | Ajinomoto Kk | COMPOSITION COSMETIQUE CONTENANT UNE Nx,Ng-DIACYLARGININE |
Also Published As
Publication number | Publication date |
---|---|
KR20030005257A (ko) | 2003-01-17 |
EP1269969A4 (en) | 2003-10-08 |
US20040052747A1 (en) | 2004-03-18 |
EP1269969A1 (en) | 2003-01-02 |
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