WO2005117815A1 - 毛髪形状制御剤 - Google Patents
毛髪形状制御剤 Download PDFInfo
- Publication number
- WO2005117815A1 WO2005117815A1 PCT/JP2005/010239 JP2005010239W WO2005117815A1 WO 2005117815 A1 WO2005117815 A1 WO 2005117815A1 JP 2005010239 W JP2005010239 W JP 2005010239W WO 2005117815 A1 WO2005117815 A1 WO 2005117815A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- hair
- agent
- acid
- mass
- control agent
- 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
- A61K8/43—Guanidines
-
- 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
- A61Q5/06—Preparations for styling the hair, e.g. by temporary shaping or colouring
Definitions
- the present invention provides a hair shape control that contains a guanidine derivative, can permanently cure natural curly hair, and does not damage hair and at the same time does not give a dry feeling.
- the first agent is a hair shape control that contains a guanidine derivative, can permanently cure natural curly hair, and does not damage hair and at the same time does not give a dry feeling.
- the first agent is a hair shape control that contains a guanidine derivative
- Patent Document 1 JP-A-60-21704
- Patent Document 2 JP-A-59-90508
- Patent document 3 JP-A-10-17441
- Patent document 4 JP-A-10-17442
- Patent Document 5 JP-A-2004-75588
- the present invention provides a first hair shape controlling agent comprising the following components (A) to (C).
- R 1 represents a linear or branched alkyl group having 6 to 12 carbon atoms.
- R 2 represents a linear or branched alkyl group having 8 to 18 carbon atoms, and n represents a number of 1 to 25. ]
- the present invention relates to a hair treatment composition capable of permanently curling natural curly hair, and which does not give any damage or dryness to hair.
- the inventor of the present invention has proposed that the use of a combination of a keratin-reducing substance, a guanidine derivative represented by the general formula (1) or an acid addition salt thereof, and a specific surfactant will result in natural curly hair. It has been found that it is possible to obtain the first agent, a hair shape control agent that has an excellent hair modifying effect, such as permanent straightening of the hair and permanent setting of the hair, and that does not damage or dry the hair. Was.
- the keratin-reducing substance of component (A) may be any compound having a reducing ability to keratin, which is a structural protein of hair, and may be, for example, thioglycolic acid, a thioglycolic acid derivative, or thioglycolic acid. Or a salt of a thioglycolic acid derivative, a cysteine, a salt of a cysteine or a cysteine derivative, a sulfite, a bisulfite, a compound represented by the following general formula (3):
- R 3 is a hydrogen atom, a linear or branched alkyl group having 1 to 4 carbon atoms, or R—O
- R is a linear or branched alkyl group having 1 to 4 carbon atoms, R is a methylene group or carbon b a b
- the thioglyceryl alkyl ether represented by the following, derivatives and salts thereof, [0017] [Dani 4]
- thioglycolic acids include thioglycolic acid and glyceryl esters thereof; cysteines include L-cysteine, D-cysteine, N-acyl cysteine, and the like; salts of these cysteines As ammonium salts, quaternary ammonium salts and alkanolamine salts (monoethanolamine salts, diethanolamine salts, triethanolamine salts, etc.); sulfites as sodium sulfite; bisulfites as sulfurous acid Sodium hydrogen, etc .; thioglyceryl alkyl ethers include ethoxyhydroxypropanethiol, ethoxyethoxyhydroxypropanethiol, methoxyethoxyhydroxypropanethiol, isopropoxyethoxyhydroxypropanethiol, etc .; mercaptoalkylamido The, mercapto E chill pro Pana bromide, mercapto E
- the keratin-reducing substance of the component (A) can be used alone or in combination of two or more, and it is particularly preferable to mix 0.1 to 20% by mass in the first part of the hair shape controlling agent. When the content is 3 to 20% by mass, reduction can be sufficiently achieved and the skin and hair are not damaged, which is preferable.
- the guanidine derivative of the component (B) is represented by the general formula (1).
- examples of the linear or branched alkyl group having 6 to 12 carbon atoms represented by R 1 include an n-octyl group, a 2-ethylhexyl group, a decyl group and a dodecyl group. And an n-octyl group and a 2-ethylhexyl group are particularly preferred.
- the guanidine derivative (1) of the component (B) may form an acid addition salt with any physiologically acceptable acid.
- Examples of the acid used in the acid addition salt include: Either an organic acid or an inorganic acid can be used.
- organic acids such as acetic acid, propionic acid, butyric acid, isobutyric acid, glycolic acid, lactic acid, succinic acid, malic acid, and other organic carboxylic acids, methanesulfonic acid, isethionic acid, amino acids
- Examples include lower alkyl sulfonic acids such as ethyl sulfonic acid and the like, and aryl sulfonic acids such as benzene sulfonic acid, p-toluene sulfonic acid, nitrobenzene sulfonic acid, xylene sulfonate and cumene sulfonic acid.
- the inorganic acid include hydrochloric acid such as hydrochloric acid, hydrobromic acid, and hydroiodic acid, and perchloric acid, sulfuric acid, nitric acid, phosphoric acid,
- the guaridine derivative of component (B) or the acid addition salt thereof may be used in combination of two or more kinds, and the content thereof is from the viewpoint of the hair straightening effect, from the viewpoint of the hair straightening effect of the present invention. It is preferably at least 1% by mass, more preferably at least 3% by mass, particularly preferably at least 5% by mass in the first agent. Further, the upper limit of the content is preferably 20% by mass or less, more preferably 18% by mass or less, and particularly preferably 15% by mass or less.
- the nonionic surfactant of the component (C) is a polyoxyethylene alkyl ether represented by the general formula (2).
- R 2 is a linear or branched alkyl group having 8 to 18 carbon atoms, and the average number of moles of added ethylene oxide group n is 1 to 25. Further, n is preferably 2 to 25, particularly preferably 6 to 23.
- Component (C) the number of carbon atoms in R 2 is the same n different, or n is a a mixture be Yogu their mixtures of different compounds the carbon number of the same a R 2 may be used in combination of two or more .
- component (C) examples include Emulgen 102K, Emalgen 103, Emalgen 104 ⁇ , Emanolegen 106, Emanolegen 109 ⁇ , Emanolegen 123 ⁇ , Emanolegen 150, Emalgen 1620G, Emalgen 220 etc. (above, Kao Corporation), NIKKOLBL-2, NIKKOLBL-9EX, NIKKOLBD-4, etc. (above, Nikko Chemicals Co., Ltd.).
- the content of the nonionic surfactant of the component (C) is 0.1 to 20% by mass, particularly 3 to 18% by mass in the first part of the hair shape controlling agent of the present invention from the viewpoint of the hair straightening effect. Is preferred.
- the polyol having a relatively short alkyl chain length and a small number of moles of EO addition is used. It is preferable to use xylene ethylene ether.
- an organic carboxylic acid addition salt such as lactate is used as the acid addition salt of the guanidine derivative, the alkyl chain length is relatively long and the EO addition mole number is large! /, Polyoxyethylene alkyl ether. It is preferable to use for example, for sulfates and carbonates of guadin derivatives,
- R 2 in the general formula (2) is a linear alkyl group having 8 to 12 carbon atoms, particularly 8 to 10 carbon atoms, and n is 2 to 10, particularly 6 to 9 polyoxyethylene alkyl ether. It is preferable to use
- R 2 in the general formula (2) is an alkyl group having 14 to 18 carbon atoms, particularly 16 to 18 carbon atoms. It is preferable to use a polyoxyethylene alkyl ether having a force n of 11 to 25, particularly 16 to 20.
- the weight ratio of the guanidine derivative of the component (B) to the nonionic surfactant of the component (C) is 5: 1 to 1: 5, particularly It is preferable to use 2: 1 to 1: 1.
- the first hair shape controlling agent of the present invention further contains glycine betaine (trimethylglycine) as the component (D) from the viewpoint of hair deformation effect (wave effect, curly hair straightening effect) and feel. You can have.
- glycine betaine for example, those commercially available as Aminocoat (Asahi Kasei Kogyo Co., Ltd.) can be used.
- Glycine betaine is preferably contained in the first part of the hair shape controlling agent of the present invention in an amount of 0.1 or more, more preferably 1.5% by mass or more, particularly preferably 2% by mass or more. From the viewpoint of the stability of the composition, the upper limit of the content is preferably 12% by mass or less, more preferably 10% by mass or less, and particularly preferably 8% by mass or less.
- the first agent for controlling the hair shape of the present invention preferably uses ammonia or a salt thereof, a power capable of being made alkaline with an alkali agent such as an alkanolamine, ammonia or a salt thereof, and monoethanolamine.
- the pH of the first part of the hair shape controlling agent is preferably adjusted to 5 to 11, more preferably 6 to 10, particularly preferably 7 to 9.6.
- the hair shape controlling agent of the present invention is formed into a jell system using a natural polymer or a synthetic polymer.
- the natural polymer and the synthetic polymer that can be used here include dimethyldiarylammonium-acrylamide copolymer (for example, Mercoat 100, Marcoat 550 (all above, Calgon)), Burr Pyrrolidone'dimethylaminoethyl methacrylate copolymer [eg, copolymer 845, copolymer 937, copolymer 958 (all from GAF)], o- [2-hydroxy-3- (lauryl dimethylammono) propyl] hydroxy chloride Ethylcellulose [For example, Polymer JR-125, JR-30M, JR-400 (Union Carbide) Ogard G (Lion Co., Ltd.)], Shiojiri 0- [2-hydroxy-3- (trimethylammono) propyl] guar gum [for example, Labor gum
- Two or more of these natural polymers and synthetic polymers can be used in combination, and the content thereof is 0.05 to 20% by mass in the first hair shape controlling agent of the present invention. 0.1-10 mass%, especially 0.5-5 mass% is preferred.
- the first hair shape controlling agent of the present invention may contain an organic solvent.
- organic solvent examples include monohydric alcohols such as ethanol; monohydric or polyhydric aromatic alcohols such as 2-phenoxyethanol, benzyl alcohol, 2-phenylethanol, and 2-benzyloxyethanol; triethylene Glycols such as glycol, 1,3-butylene glycol, propylene glycol, hexylene glycol, and diethylene glycol; ethylene glycolone methylene etherate, ethylene glycolone ethylenate ethereene, ethylene glycolone mono-n-butyl ether, propylene glycol monomethyl ether Glycol ethers such as diethyleneglycol monomethinooleatenole, diethyleneglycololenothenoleateneole, diethyleneglycolmono n-butyl ether; N-methylpyrrolidone, N-ethylpyrrolidone, etc.
- monohydric alcohols such as ethanol
- monohydric or polyhydric aromatic alcohols such as 2-phenoxyethanol,
- N-alkylpyrrolidone alkylene carbonate such as ethylene carbonate and propylene carbonate
- ratatones such as ⁇ -butyrolataton, ⁇ -valerolatatone, and ⁇ -force prolataton.
- Two or more of these organic solvents can be used in combination, and the content thereof is 0.05 to 20% by mass, more preferably 0.1 to 10% by mass in the first hair shape controlling agent of the present invention. And particularly preferably 0.5 to 5% by mass.
- the components used in the ordinary first part of the perm solution and the components used in the field of cosmetics are added according to the purpose. be able to.
- Such optional components include inorganic alkalis, fatty acids, fats and oils, hydrocarbons, silicone derivatives, surfactants other than component (C), amino acid derivatives, protein derivatives, chelating agents, preservatives, and antioxidants.
- Curling and hair straightening using the first hair shape controlling agent of the present invention can be performed in the same manner as conventional perms (straight, wave, iron).
- conventional perms straight, wave, iron
- the first agent is impregnated into the hair
- the hair is impregnated with a second agent containing an oxidizing agent following the first agent treatment step.
- the hair is removed from the curlers and rods, washed with water and dried.
- an intermediate treatment step of washing the hair with water or rinsing with an acidic treatment liquid may be used.
- the first agent treatment step the first agent is applied to the straight hair using a crumpled brush, and the straight hair is shaped.
- the second agent is applied to the hair using a brush.
- an intermediate treatment step may be performed between the first treatment step and the second treatment step, in which the hair is rinsed with water or rinsed with an acidic treatment liquid. After the second treatment step for a predetermined time, the hair is washed with water and dried.
- the application amount of the first hair shape controlling agent of the present invention is preferably 0.1 to 4 times by mass, particularly preferably 0.5 to 2.5 times by mass with respect to the hair to be treated.
- the treatment time of the hair with the first part of the hair shape controlling agent of the present invention is appropriately adjusted in the range of 1 to 120 minutes depending on the strength, thickness and damage of the hair to be treated. In this case, if necessary, the temperature can be increased to 30 to 55 ° C, especially 35 to 50 ° C. /.
- a higher straightening effect is obtained by using a flat iron It is also possible.
- the hair force first agent is washed off, dried with a drier, and then ironed.
- the temperature of the iron is preferably set at 120 to 180 ° C, particularly 140 to 180 ° C.
- the second part used subsequently to the first part of the hair shape controlling agent of the present invention contains an oxidizing agent.
- the oxidizing agent include bromate, perborate, hydrogen peroxide and the like, and examples of the bromate and perborate include sodium salt, potassium salt, and ammonium salt.
- the content of the oxidizing agent is preferably 0.5 to 3% by mass, more preferably 0.75 to 2.5% by mass in the second agent, from the viewpoint of a hair straightening effect and prevention of hair damage.
- components used in ordinary second agents and components used in the cosmetic field can be added according to the purpose. The standing time during the treatment is appropriately adjusted between 1 and 30 minutes.
- a treating agent containing a hair protection component or the like can be separately used in combination.
- the first hair shape control agent (test solution) shown in Table 1 was prepared.
- the test solution was heated to 60 ° C., vigorously stirred for 1 hour, allowed to stand at room temperature for 12 hours, and the state of dissolution was visually evaluated according to the following criteria.
- the first part shown in Table 2 and the second part shown in Table 3 were prepared, and the hair straightening effect and the feeling of shortness of the treated hair when the hair was treated with them were compared.
- Tresses were made with curly hair with a curl radius ⁇ of about 5 to 8 mm without chemical treatment such as perm and hair color. The first part is applied to this, left for 1 hour, and then washed with water. After applying the second agent to this and leaving it to stand for 20 minutes, wash and dry. According to the following criteria, the effect of straightening the curly hair and the feeling of shortness were determined.
- Examples 1 to 8 containing the components (A) to (C) were all good results. Comparative Examples 1 to 6, in which propanol was used for dissolving the guanidine derivative, showed a feeling just before. Comparative Examples 7 and 8, which did not contain a guanidine derivative, were inferior in the hair straightening effect.
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- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Birds (AREA)
- Epidemiology (AREA)
- Cosmetics (AREA)
Abstract
Description
Claims
Priority Applications (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN2005800175895A CN1960697B (zh) | 2004-06-03 | 2005-06-03 | 毛发形状控制剂 |
EP05746049A EP1752130A1 (en) | 2004-06-03 | 2005-06-03 | Hair style control agent |
BRPI0511795-0A BRPI0511795A (pt) | 2004-06-03 | 2005-06-03 | agente de controle de estilo do cabelo |
US11/628,270 US20070248554A1 (en) | 2004-06-03 | 2005-06-03 | Hair Style Control Agent |
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2004166020 | 2004-06-03 | ||
JP2004-166020 | 2004-06-03 | ||
JP2005-162176 | 2005-06-02 | ||
JP2005162176A JP2006335682A (ja) | 2005-06-02 | 2005-06-02 | 毛髪形状制御剤 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2005117815A1 true WO2005117815A1 (ja) | 2005-12-15 |
Family
ID=35462709
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/JP2005/010239 WO2005117815A1 (ja) | 2004-06-03 | 2005-06-03 | 毛髪形状制御剤 |
Country Status (5)
Country | Link |
---|---|
US (1) | US20070248554A1 (ja) |
EP (1) | EP1752130A1 (ja) |
CN (1) | CN1960697B (ja) |
BR (1) | BRPI0511795A (ja) |
WO (1) | WO2005117815A1 (ja) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7704939B2 (en) * | 2004-08-31 | 2010-04-27 | Sanyo Chemical Industries, Ltd. | Surfactant |
Families Citing this family (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2901472B1 (fr) | 2006-05-24 | 2010-08-13 | Oreal | Procede de defrisage des fibres keratiniques avec un moyen de chauffage et des agents denaturants |
US8603448B2 (en) | 2006-06-05 | 2013-12-10 | L'oreal | Use of a non-hydroxide base with heat for relaxing or straightening hair |
DE102007017440A1 (de) * | 2007-04-11 | 2008-10-16 | Beiersdorf Ag | Octanoat-haltige Zubereitung mit 2-(4'-Diethylamino-2'-hydoxybenzoyl)-benzoesäurehexylester |
ES2682267T3 (es) * | 2008-03-19 | 2018-09-19 | L'oréal | Composición de alisado del pelo de una base no de hidróxido y un desnaturalizante de proteínas y procedimiento |
JP6657403B2 (ja) * | 2015-12-04 | 2020-03-04 | ザ プロクター アンド ギャンブル カンパニーThe Procter & Gamble Company | 縮毛を減少させるための組成物 |
WO2020000419A1 (en) * | 2018-06-29 | 2020-01-02 | L'oreal | Method for shaping and/or waving keratin fibres comprising the application of a thiol-comprising reducing agent and a salt of guanidine, composition and use thereof |
Citations (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5679618A (en) * | 1979-11-30 | 1981-06-30 | Tanabe Seiyaku Co Ltd | Liquid for permanent wave |
JPS60181009A (ja) * | 1984-02-28 | 1985-09-14 | Shiseido Co Ltd | パ−マネントウエ−ブ用剤第1剤 |
JPH03236309A (ja) * | 1990-02-09 | 1991-10-22 | Tamura Jishiyoudou:Kk | 育毛剤の製造方法 |
JPH06293621A (ja) * | 1993-04-09 | 1994-10-21 | Asahi Chem Ind Co Ltd | パ−マ液 |
JPH1017442A (ja) * | 1996-07-04 | 1998-01-20 | Kao Corp | 毛髪処理剤組成物 |
JP2000297017A (ja) * | 1999-04-13 | 2000-10-24 | Sanei Kagaku Kk | 毛髪硬化処理剤及びそれを含有したコールドウェーブ処理剤 |
JP2001328928A (ja) * | 2000-05-22 | 2001-11-27 | Seiwa Kasei:Kk | 酸性染毛料 |
JP2003286141A (ja) * | 2002-03-29 | 2003-10-07 | Mandom Corp | クリーム状一剤式縮毛矯正剤 |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB9109775D0 (en) * | 1991-05-04 | 1991-06-26 | Procter & Gamble | Cosmetic compositions |
EP0538762B1 (en) * | 1991-10-22 | 1996-04-10 | Kao Corporation | Hair cosmetic |
-
2005
- 2005-06-03 CN CN2005800175895A patent/CN1960697B/zh not_active Expired - Fee Related
- 2005-06-03 US US11/628,270 patent/US20070248554A1/en not_active Abandoned
- 2005-06-03 EP EP05746049A patent/EP1752130A1/en not_active Withdrawn
- 2005-06-03 BR BRPI0511795-0A patent/BRPI0511795A/pt not_active Application Discontinuation
- 2005-06-03 WO PCT/JP2005/010239 patent/WO2005117815A1/ja not_active Application Discontinuation
Patent Citations (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5679618A (en) * | 1979-11-30 | 1981-06-30 | Tanabe Seiyaku Co Ltd | Liquid for permanent wave |
JPS60181009A (ja) * | 1984-02-28 | 1985-09-14 | Shiseido Co Ltd | パ−マネントウエ−ブ用剤第1剤 |
JPH03236309A (ja) * | 1990-02-09 | 1991-10-22 | Tamura Jishiyoudou:Kk | 育毛剤の製造方法 |
JPH06293621A (ja) * | 1993-04-09 | 1994-10-21 | Asahi Chem Ind Co Ltd | パ−マ液 |
JPH1017442A (ja) * | 1996-07-04 | 1998-01-20 | Kao Corp | 毛髪処理剤組成物 |
JP2000297017A (ja) * | 1999-04-13 | 2000-10-24 | Sanei Kagaku Kk | 毛髪硬化処理剤及びそれを含有したコールドウェーブ処理剤 |
JP2001328928A (ja) * | 2000-05-22 | 2001-11-27 | Seiwa Kasei:Kk | 酸性染毛料 |
JP2003286141A (ja) * | 2002-03-29 | 2003-10-07 | Mandom Corp | クリーム状一剤式縮毛矯正剤 |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7704939B2 (en) * | 2004-08-31 | 2010-04-27 | Sanyo Chemical Industries, Ltd. | Surfactant |
Also Published As
Publication number | Publication date |
---|---|
CN1960697A (zh) | 2007-05-09 |
US20070248554A1 (en) | 2007-10-25 |
CN1960697B (zh) | 2011-09-21 |
EP1752130A1 (en) | 2007-02-14 |
BRPI0511795A (pt) | 2008-01-15 |
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