WO2009099007A1 - 洗浄料 - Google Patents
洗浄料 Download PDFInfo
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- WO2009099007A1 WO2009099007A1 PCT/JP2009/051571 JP2009051571W WO2009099007A1 WO 2009099007 A1 WO2009099007 A1 WO 2009099007A1 JP 2009051571 W JP2009051571 W JP 2009051571W WO 2009099007 A1 WO2009099007 A1 WO 2009099007A1
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- 0 C*NOC(C)(C)N(*C)O*C Chemical compound C*NOC(C)(C)N(*C)O*C 0.000 description 1
- FTYHOENHAVIGCQ-UHFFFAOYSA-N CCC(C)(N(N)O[N](C)([N]#C)[N]#C)ON([N]#C)O Chemical compound CCC(C)(N(N)O[N](C)([N]#C)[N]#C)ON([N]#C)O FTYHOENHAVIGCQ-UHFFFAOYSA-N 0.000 description 1
Classifications
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- 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
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- 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
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- 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
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- 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
- A61K8/58—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing atoms other than carbon, hydrogen, halogen, oxygen, nitrogen, sulfur or phosphorus
- A61K8/585—Organosilicon compounds
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q1/00—Make-up preparations; Body powders; Preparations for removing make-up
- A61Q1/14—Preparations for removing make-up
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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
- A61Q5/02—Preparations for cleaning the hair
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- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/02—Anionic compounds
- C11D1/04—Carboxylic acids or salts thereof
- C11D1/06—Ether- or thioether carboxylic acids
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- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/02—Anionic compounds
- C11D1/12—Sulfonic acids or sulfuric acid esters; Salts thereof
- C11D1/28—Sulfonation products derived from fatty acids or their derivatives, e.g. esters, amides
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- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/162—Organic compounds containing Si
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- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/37—Polymers
- C11D3/3703—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C11D3/373—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds containing silicones
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- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D9/00—Compositions of detergents based essentially on soap
- C11D9/04—Compositions of detergents based essentially on soap containing compounding ingredients other than soaps
- C11D9/22—Organic compounds, e.g. vitamins
- C11D9/225—Polymers
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- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D9/00—Compositions of detergents based essentially on soap
- C11D9/04—Compositions of detergents based essentially on soap containing compounding ingredients other than soaps
- C11D9/22—Organic compounds, e.g. vitamins
- C11D9/36—Organic compounds, e.g. vitamins containing silicon
Definitions
- the present invention relates to a cleaning material containing an organosiloxane derivative having a specific structure, particularly to coexistence of foaming and cleaning properties.
- organo (poly) siloxanes in which various organic groups are introduced into a part of the structure have been developed taking advantage of the unique characteristics of dimethylpolysiloxane, which is representative of silicone oil.
- Organo (poly) siloxane has low surface tension, low refractive index, and low friction, heat resistance, cold resistance, antistatic properties, water repellency, releasability, antifoaming properties, chemical resistance, etc. Is used in various fields.
- organo (poly) siloxanes in which various functional groups and structural positions for introducing them are modified.
- Organo (poly) siloxane derivative containing a carboxyl group which is a hydrophilic organic group
- various compounds have been developed and studied so far.
- Organosiloxane derivatives having a carboxyl group introduced are widely known.
- siloxane dendrimers containing a carboxyl structure have been reported as an example of such compounds (see, for example, Patent Documents 1 to 3).
- Patent Documents 1 to 3 siloxane dendrimers containing a carboxyl structure
- a compound obtained by neutralizing carboxyl-modified silicone with triethanolamine has an emulsifying ability (see, for example, Non-Patent Documents 1 and 2).
- an anionic surfactant or a nonionic surfactant is usually blended as a main component of the cleanser.
- most makeup products, hair waxes, etc. are formulated with a silicone compound for the purpose of imparting makeup durability, water resistance, slipperiness and smoothness, and using a normal surfactant as a cleaning agent.
- a normal surfactant as a cleaning agent.
- foaming is very bad due to the defoaming effect, although the cleaning effect is enhanced by blending silicone oil or using a silicone-based surfactant.
- the present invention has been made in view of the above-described circumstances, and an object thereof is to provide a cleaning material having both excellent foaming and cleaning properties.
- the organosiloxane derivative salt having a specific structure containing a carboxyl group and an anionic surfactant such as fatty acid soap are used as cleaning agents.
- an anionic surfactant such as fatty acid soap
- the cleaning material according to the present invention includes an organosiloxane derivative salt represented by the following general formula (1) or the following general formula (3), a carboxylate having 10 to 20 carbon atoms, a sulfate, It contains any one or more of sulfonate and phosphate.
- organosiloxane derivative salt represented by the following general formula (1) or the following general formula (3), a carboxylate having 10 to 20 carbon atoms, a sulfate, It contains any one or more of sulfonate and phosphate.
- R 1 to R 3 may be the same or different substituted or unsubstituted monovalent hydrocarbon groups.
- M is a metal atom or an organic cation
- A is a linear or branched alkylene group represented by C q H 2q
- q is an integer of 0 to 20.
- the average total number of silicon atoms (Si) contained in one molecule of the organosiloxane derivative represented by 1) is 2 to 10 In is.
- R 6 is a hydrogen atom, an alkyl group having 1 to 6 carbon atoms, or a phenyl group
- R 7 and R 8 are either an alkyl group having 1 to 6 carbon atoms or a phenyl group.
- B is a linear or branched alkylene group represented by C r H 2r which may be partially branched, and r is an integer of 2 to 20.
- R 9 to R 12 are substituted or unsubstituted monovalent hydrocarbon groups which may be the same or different, M is a metal atom or an organic cation, Q is C q H 2q A linear or branched alkylene group represented by the formula, q is an integer of 0 to 20, and p is a number of 0 to 100.
- the organosiloxane derivative should be represented by the formula (1)
- the functional group (R 4 R 1 and R 2 is represented by -O-Si (R 4) 3 is a C1- R 3 is a monovalent hydrocarbon group having 1 to 10 carbon atoms, and q is preferably an integer of 6 to 20.
- the organosiloxane derivative is represented by the general formula (1), and at least one of R 1 to R 3 is a functional group represented by the following general formula (4) or (5). It is preferable that the other R 1 to R 3 are substituted or unsubstituted monovalent hydrocarbon groups which may be the same or different.
- the organosiloxane derivative is represented by the general formula (3), and R 9 to R 12 are each a substituted or unsubstituted alkyl group having 1 to 20 carbon atoms, an aryl group, and an aralkyl group. It is preferable that q is a group selected from the group, q is an integer of 6 to 20, and p is a number of 1 to 20.
- the anionic surfactant is at least one of fatty acid soap, acylmethyl taurate, and alkyl ether carboxylate.
- an organosiloxane derivative salt having a specific structure containing a carboxyl group and an anionic surfactant such as fatty acid soap into the cleaning agent, the cleaning effect is excellent and the foaming property is remarkably improved. Is done.
- the cleaning agent according to the present invention is characterized by containing an organosiloxane derivative salt having a specific structure containing a carboxyl group and an anionic surfactant such as fatty acid soap.
- Organosiloxane derivative used in the present invention is a compound represented by formula (1) or formula (3). First, the organosiloxane derivative represented by the following general formula (1) will be described.
- the organosiloxane derivative represented by the general formula (1) is an organosiloxane derivative modified with an alkylcarboxyl group, characterized in that the average total number of silicon atoms in one molecule is in the range of 2 to 100. To do.
- at least one of R 1 to R 3 is a functional group represented by —O—Si (R 4 ) 3 (R 4 is an alkyl group having 1 to 6 carbon atoms or a phenyl group.
- R 1 to R 3 may be any of the functional groups.
- other R 1 ⁇ R 3 is any one of the same or may be different substituted or unsubstituted monovalent hydrocarbon group Also good.
- R 4 is either an alkyl group having 1 to 6 carbon atoms or a phenyl group.
- alkyl group having 1 to 6 carbon atoms include methyl, ethyl, n-propyl, i-propyl, n-butyl, i-butyl, s-butyl, t-butyl, pentyl, neopentyl, cyclopentyl, hexyl and the like. Examples include linear, branched or cyclic alkyl groups.
- Examples of the functional group represented by —O—Si (R 4 ) 3 include —O—Si (CH 3 ) 3 , —O—Si (CH 3 ) 2 (C 2 H 5 ), —O—Si. (CH 3 ) 2 (C 3 H 7 ), —O—Si (CH 3 ) 2 (C 4 H 9 ), —O—Si (CH 3 ) 2 (C 5 H 11 ), —O—Si (CH 3 ) 2 (C 6 H 13 ), —O—Si (CH 3 ) 2 (C 6 H 5 ), and the like.
- the functional group is preferably a trialkylsiloxy group, and most preferably a trimethylsiloxy group.
- the functional group represented by —O—Si (R 5 ) 2 —X 1 is an organosiloxy group having a dendrimer structure, and R 5 is either an alkyl group having 1 to 6 carbon atoms or a phenyl group. It is.
- R 6 is any one of a hydrogen atom, an alkyl group having 1 to 6 carbon atoms, or a phenyl group
- R 7 and R 8 are an alkyl group or phenyl group having 1 to 6 carbon atoms.
- R 6 to R 8 are preferably alkyl groups having 1 to 6 carbon atoms, and particularly preferably all methyl groups.
- B is a linear or branched alkylene group represented by C r H 2r which may be partially branched, and r is an integer of 2 to 20.
- alkylene group having 2 to 20 carbon atoms as B examples include linear alkylene groups such as ethylene group, propylene group, butylene group and hexylene group; methylmethylene group, methylethylene group, 1-methylpentylene group, 1, Examples thereof include branched alkylene groups such as 4-dimethylbutylene group. Among these, an ethylene group or a hexylene group is preferable.
- i specifies the generation of a silylalkyl group represented by X i, the number of layers, i.e., the number of repetitions of the silylalkyl group is an integer ranging from 1 ⁇ n when n.
- the number n of layers is an integer from 1 to 10.
- ai is preferably 1 or less, particularly preferably 0. That is, when the layer n of the dendrimer structure is 1, the silylalkyl group of the formula (2) is
- the functional group represented by —O—Si (R 5 ) 2 —X 1 is particularly preferably a functional group in which the number n of tiers of the silylalkyl group represented by the following general formula (4) is 1, or the following general group A functional group in which the number n of layers of the silylalkyl group represented by the formula (5) is 2 or a functional group in which the number of layers n of the silylalkyl group represented by the following general formula (6) is 3 is exemplified.
- R 1 to R 3 is a functional group represented by the aforementioned —O—Si (R 4 ) 3 , or —O—Si (R 5 ) 2.
- the other R 1 to R 3 may be either substituted or unsubstituted monovalent hydrocarbon groups which may be the same or different. .
- Examples of the unsubstituted monovalent hydrocarbon group represented by R 1 to R 3 include methyl, ethyl, n-propyl, i-propyl, n-butyl, i-butyl, s-butyl, pentyl, neopentyl, cyclopentyl, hexyl, etc.
- Examples of the substituted monovalent hydrocarbon group represented by R 1 to R 3 include perfluoroalkyl groups such as 3,3,3 trifluoropropyl group, 3,3,4,4,4-pentafluorobutyl group; Examples include aminoalkyl groups such as aminopropyl group and 3- (aminoethyl) aminopropyl group; and amidealkyl groups such as acetylaminoalkyl group.
- a part of the hydrocarbon groups of R 1 to R 3 may be substituted with a hydroxyl group, an alkoxy group, a polyether group or a perfluoropolyether group, and as the alkoxy group, a methoxy group, an ethoxy group, a propoxy group Is exemplified.
- R 1 to R 3 are a functional group represented by the above —O—Si (R 4 ) 3 , or —O—Si (R 5 ) 2 —X 1
- the other R 1 to R 3 are preferably straight-chain or branched alkyl groups having 1 to 6 carbon atoms, particularly preferably a methyl group or an ethyl group. preferable.
- R 1 to R 3 all or two of them are a functional group represented by —O—Si (R 4 ) 3 , or —O—Si (R 5 ) 2 —X 1
- the other R 1 to R 3 are preferably a methyl group or an ethyl group.
- M is a metal atom or an organic cation.
- the metal atom include a monovalent alkali metal, a divalent alkali metal, and a divalent or higher metal atom.
- the monovalent alkali metal is Li, Na, K
- the divalent alkali metal is Mg, Ca, Ba, and the others are Mn, Fe, Co, Al, Ni, Cu, V, Mo, Nb. , Zn, Ti and the like.
- organic cation examples include ammonium ion, aminomethylpropanol (AMP) neutralized ion, triethanolammonium ion, diethanolammonium ion, monoethanolammonium ion, triisopropanolammonium ion, L-arginine neutralized ion, L -Lysine neutralization ions and the like.
- M is particularly preferably a monovalent alkali metal, or may be a mixture thereof.
- A is a linear or branched alkylene group represented by C q H 2q , and q is an integer of 0 to 20.
- the organosiloxane derivative represented by the general formula (1) is a compound represented by the following general formula (1-A), and the carboxyl-modified group is bonded to silicon through an ethylene group. It is what you are doing.
- q is preferably 2 to 15, and more preferably 6 to 12.
- the foaming property may be inferior.
- the organosiloxane derivative represented by the general formula (1) is characterized in that the average total number of silicon atoms in one molecule is in the range of 2 to 100.
- the average total number of silicon atoms is preferably in the range of 3-30.
- foamability may be inferior.
- the organosiloxane derivative represented by the general formula (1) is more specifically a functional group (R 4 is a carbon number) in which R 1 and R 2 are represented by —O—Si (R 4 ) 3.
- R 4 is a functional group in which R 1 and R 2 are represented by —O—Si (R 4 ) 3.
- An organosiloxane derivative in which R 3 is a linear or branched alkyl group having 1 to 6 carbon atoms and q is 6 to 12 is preferably used. .
- the organosiloxane derivative represented by the general formula (1) has a silicon atom-bonded hydrogen atom-containing polysiloxane represented by R 1 R 2 R 3 SiH and a vinyl terminal represented by CH ⁇ CH 2 -A-COOSiMe 3.
- Carboxylic acid trimethylsilyl derivative is subjected to an addition reaction in the presence of a platinum-based catalyst, and at least 1 mol of monohydric alcohol such as methanol is added per 1 mol of the protective group, trimethylsilyl group, and heated. It can be produced by deprotection and neutralization with a compound containing a corresponding metal ion (M n + ) or a basic organic compound.
- R 1 , R 2 , R 3 , A, and M are the same groups as described above.
- an aqueous solution of sodium hydroxide (NaOH), potassium hydroxide (KOH), triethanolamine, arginine, aminomethylpropanol (AMP), or the like is added to form a carboxyl group (—COOH). This is a step of neutralization.
- R 1 to R 3 and A are the same groups as described above, and M ′ is a hydrogen atom.
- the average total number of silicon atoms (Si) contained in one molecule of the organosiloxane derivative represented by the general formula (1 ′) is 2 to 150.
- cation exchange of the terminal carboxyl group is performed by mixing the organosiloxane derivative having a terminal carboxyl group represented by the general formula (1 ′) and a solution containing a metal ion or an organic cation.
- the organosiloxane derivative represented by the general formula (1) can be easily obtained. For this reason, you may mix
- the metal ion-containing compound or basic organic compound include the same compounds as described above.
- the amount of the metal ion-containing compound or basic organic compound used relative to the organosiloxane derivative having a terminal carboxyl group represented by the general formula (1 ′) is the mass ratio of the organosiloxane derivative: metal ion-containing compound or basic organic compound.
- the range of 6: 1 to 2: 1 is suitable, but is not particularly limited.
- the method for producing the organosiloxane derivative represented by the general formula (1) is described in detail in JP-A-2000-072784, JP-A-2000-239390, and JP-A-2001-213885.
- the method for producing an organosiloxane derivative represented by the general formula (1) of the present invention can be easily produced by the following steps (1) to (4).
- R is either an alkyl group having 1 to 6 carbon atoms or a phenyl group
- R L is a substituted or unsubstituted monovalent hydrocarbon group which may be the same or different
- f is 1
- An organosilane having a dimethylsiloxy group represented by ## STR3 ## and a trimethylsilyl carboxylic acid derivative having a vinyl terminal represented by CH CH 2 -A-COOSiMe 3 (wherein A is the same group as described above)
- an addition reaction in the presence of a platinum-based transition metal catalyst to obtain an intermediate (1-1) of the lower general formula.
- R 6 , R 7 , R 8 , X i + 1 , ai is an organosilane having an alkenyl group represented by the same group and number as described above in the presence of a platinum catalyst to obtain an intermediate (1-2) of the following general formula.
- Step (3) The intermediate (1-2) is deprotected by alcoholysis by adding at least 1 mol of monohydric alcohol such as methanol, water or a mixture thereof to 1 mol of the trimethylsilyl group, which is a protecting group, and heating. Process.
- monohydric alcohol such as methanol, water or a mixture thereof
- Step (4) A step of neutralizing with a compound containing a metal ion (M n + ) or a basic organic compound.
- a neutralization step by adding an aqueous solution of sodium hydroxide (NaOH), potassium hydroxide (KOH), triethanolamine, arginine, aminomethylpropanol (AMP), etc., the carboxyl group (—COOH) is added to the inside. It is a process of summing.
- organosiloxane derivative represented by the following general formula (3) will be described.
- the organosiloxane derivative represented by the general formula (3) is an organosiloxane derivative in which both ends of the molecular chain are modified with an alkyl carboxyl group.
- R 9 to R 12 are selected from any of substituted or unsubstituted monovalent hydrocarbon groups which may be the same or different.
- the unsubstituted monovalent hydrocarbon group represented by R 9 to R 12 is a straight chain such as methyl group, ethyl group, propyl group, butyl group, pentyl group, hexyl group, heptyl group, octyl group, decyl group, dodecyl group, etc.
- Linear or branched alkenyl groups such as allyl and hexenyl groups; cycloalkyl groups such as cyclopentyl and cyclohexyl groups; aryl groups such as phenyl, tolyl and naphthyl groups
- An aralkyl group such as a benzyl group, a phenylethyl group, a phenylpropyl group, a naphthylmethyl group, or a naphthylethyl group;
- the substituted monovalent hydrocarbon group represented by R 9 to R 12 is such that a hydrogen atom bonded to a carbon atom of these groups is partially a hydroxyl group, halogen atom, epoxy group, amino group, methacryl group, mercapto group, alkoxy group
- a group substituted with an organic group such as a polyether group or a perfluoropolyether group, and a per group such as a 3,3,3-trifluoroprop
- R 9 to R 12 are preferably an alkyl group having 1 to 20 carbon atoms, an aryl group, and an aralkyl group, and 90 mol% or more of R 9 to R 12 in one molecule is a methyl group and / or a phenyl group. It is particularly preferred.
- M is a metal atom or an organic cation.
- the metal atom include a monovalent alkali metal, a divalent alkali metal, and a divalent or higher metal atom.
- the monovalent alkali metal is Li, Na, K
- the divalent alkali metal is Mg, Ca, Ba, and the others are Mn, Fe, Co, Al, Ni, Cu, V, Mo, Nb. , Zn, Ti and the like.
- organic cation examples include ammonium ion, aminomethylpropanol (AMP) neutralized ion, triethanolammonium ion, diethanolammonium ion, monoethanolammonium ion, triisopropanolammonium ion, L-arginine neutralized ion, L -Lysine neutralization ions and the like.
- M is particularly preferably a monovalent alkali metal, or may be a mixture thereof.
- Q is a linear or branched alkylene group represented by C q H 2q , and q is an integer of 0 to 20.
- the organosiloxane derivative represented by the general formula (3) is a compound represented by the following general formula (3-A), and the carboxyl-modified group is bonded to silicon via an ethylene group. Is.
- the value of q is preferably 6 to 20, and particularly preferably 6 to 12.
- the foaming property may be inferior.
- p represents the average degree of polymerization of the disubstituted polysiloxane and is a number from 0 to 150. In the present invention, p is more preferably from 1 to 20, and particularly preferably from 1 to 10. On the other hand, if p exceeds the upper limit, foaming properties may be inferior.
- R 9 to R 12 are alkyl groups having 1 to 6 carbon atoms, q is an integer of 0 to 20, and p is a number of 0 to 20.
- An organosiloxane derivative is preferably used.
- the organosiloxane derivative represented by the general formula (3) is H— (SiR 9 R 10 —O) p —SiR 11 R 12 —H (Wherein R 9 to R 12 , p and q are the same groups as described above)
- R 9 to R 12 and Q are the same groups as described above, p is the same number as described above, and M ′ is a hydrogen atom.
- the cation exchange of the terminal carboxyl group is performed by mixing the organosiloxane derivative having a terminal carboxyl group represented by the general formula (3 ′) and a solution containing a metal ion or an organic cation.
- the organosiloxane derivative represented by the general formula (3) can be easily obtained. For this reason, you may mix
- the metal ion-containing compound or basic organic compound include the same metal salts as described above.
- the amount of the metal ion-containing compound or basic organic compound used relative to the organosiloxane derivative having a terminal carboxyl group represented by the general formula (3 ′) is the mass ratio of the organosiloxane derivative: metal ion-containing compound or basic organic compound.
- the range of 6: 1 to 2: 1 is suitable, but is not particularly limited.
- the platinum-based catalyst used for producing the organosiloxane derivative represented by the general formula (1) or (3) of the present invention is a hydrosilylation reaction catalyst of a silicon-bonded hydrogen atom and an alkenyl group, and includes chloroplatinic acid, Alcohol-modified chloroplatinic acid, platinum olefin complex, platinum ketone complex, platinum vinylsiloxane complex, platinum tetrachloride, platinum fine powder, alumina or silica carrier with solid platinum, platinum black, platinum Examples include olefin complexes, platinum alkenylsiloxane complexes, platinum carbonyl complexes, and thermoplastic organic resin powders such as methyl methacrylate resins, polycarbonate resins, polystyrene resins, and silicone resins containing these platinum-based catalysts. Preferred is a 1,3-divinyl-1,1,3,3-tetramethyldisiloxane complex of platinum or chloroplatinic acid.
- the organosiloxane derivative represented by the said General formula (1) or the said General formula (3) can be mix
- the organosiloxane derivative represented by the above general formula (1 ′) or the above general formula (3 ′) is obtained by blending a metal ion-containing compound or a basic organic compound in a cleaning material together with the organosiloxane derivative.
- the compounding amount of the organosiloxane derivative to the cleaning material of the present invention is not particularly limited, but is usually 0.1 to 30% by mass, preferably 1 to 10% by mass, more preferably the total amount of the composition. 3 to 5% by mass. If the amount of the organosiloxane derivative is too small, a sufficient cleaning effect on the silicone compound cannot be obtained, and if the amount is too large, foaming may deteriorate.
- Anionic surfactant used in the present invention is a carboxylate, sulfate, sulfonate, or phosphate having an alkyl group having 10 to 20 carbon atoms (hereinafter simply referred to as various anionic surfactants). It may be referred to as an agent).
- various anionic surfactants are salts of various acids having a saturated or unsaturated alkyl group, and the alkyl chain may be either linear or branched. In addition to the alkyl chain, it may have another functional group (for example, amino group, ether group, etc.) or a chain structure (for example, polyoxyalkylene group, etc.).
- the various acids may be blended in the cleaning material in the form of a salt in advance, or the various acids and the basic substance for forming the salt are individually washed. It may be blended in the composition to form a salt within the formulation.
- the alkyl carboxylic acid potassium salt is formed by a neutralization reaction within the formulation.
- Examples of basic substances that form salts upon neutralization with various acids include hydroxides of alkali metals such as potassium hydroxide and sodium hydroxide, 2-amino-2-methyl-1-propanol, 2-amino-2-methyl-1,3-propanediol, triethanolamine, diethanolamine, monoethanolamine, triisopropanolamine, 2-amino-2-hydroxymethyl-1,3-propanediol, L-arginine, L -Basic nitrogen-containing compounds such as lysine, morpholine, N-alkyl taurine salts and the like.
- Examples of the carboxylate, sulfate, sulfonate, or phosphate having an alkyl group having 10 to 20 carbon atoms used in the present invention include potassium laurate, sodium laurate, triethanolamine laurate, and myristin.
- fatty acid soaps acylmethyl taurate salts, or alkyl ether carboxylates
- fatty acid soaps acylmethyl taurate salts, or alkyl ether carboxylates
- a combination with a fatty acid soap is preferable
- a combination with an acylmethyl taurate is preferable.
- the amount of the various anionic surfactants added to the cleaning material of the present invention is not particularly limited, but is usually 0.1 to 10% by mass, preferably 0.1 to 5% by mass, based on the total amount of the composition. %, More preferably 0.3 to 2% by mass. If the amount of the various anionic surfactants is too small, good foaming cannot be obtained, and if the amount is too large, there may be a problem in terms of skin irritation.
- an appropriate amount of a surfactant other than the above-mentioned various anionic surfactants for example, a nonionic surfactant, a cationic surfactant, an amphoteric surfactant, etc. is blended. It doesn't matter.
- ingredients used in the normal cosmetics and pharmaceutical fields such as oil, Wax, moisturizer (eg, ethylene glycol, propylene glycol, 1,3-butylene glycol, glycerin, polyglycerin, sorbitol, polyethylene glycol, hyaluronic acid, chondroitin sulfate, pyrrolidone carboxylate, etc.), thickener, gelling agent , Water-soluble polymers (eg, xanthan gum, carboxymethylcellulose and carboxyvinyl polymers, alkyl-modified carboxyvinyl polymers, hyaluronic acid, etc.), oil-soluble polymers, amino acids (eg, serine, arginine, etc.), drugs (eg, vitamin C, Vitamin C derivative, 4-metoki Salicylic acid, tranexamic acid, etc.), antioxidants (eg.
- the use of the detergent of the present invention is not particularly limited, and examples thereof include solid soap, liquid soap, facial scrub, facial foam, makeup remover (cleansing), skin cleanser such as body shampoo, shampoo, It can be used for various cleaning materials such as hair cleaning materials such as rinse-in shampoos.
- organosiloxane derivatives compounds 1 to 4 and comparative compounds 1 to 4 used in the examples and comparative examples are shown below.
- Each compound was identified by 1 H, 13 C, 29 Si-NMR (NMR apparatus: Fourier Transform Nuclear Magnetic Resonance Spectrometer JEOL JNM-EX400 (manufactured by JEOL Ltd.)).
- the present inventors examined the suitability as a detergent component using various organosiloxane derivatives prepared as described above.
- Each composition shown in the following Tables 1 to 3 was prepared and evaluated for various usability of foaming, makeup removal, and hair wax removal.
- the compositions used in the tests and the evaluation results are shown in Tables 1 to 3 below.
- the contents of the test are as shown below.
- Foaming (Evaluation criteria) 5 points: Good foaming (a lot of foam) 4 points: Slightly good foaming (a little amount of foam) 3 points: Normal 2 points: Slightly bad foaming (a little amount of foam) 1 point: Poor foaming (the amount of foam is small) Make-up (based on evaluation points) 5 points: Make-up is good 4 points: Make-up is good 3 points: Normal 2 points: Make-up is slightly bad 1 point: Make-up is bad Hair wax drops (evaluation criteria) 5 points: Good hair wax removal 4 points: Good hair wax removal 3 points: Normal 2 points: Some hair wax is bad 1 point: Hair wax removal is bad
- Comparative Example 3 using a silicone group-short organosiloxane derivative was inferior in terms of detergency, and a silicone group-long organosiloxane derivative (Comparative Compounds 2 to 2).
- Comparative Examples 4 to 6 using 4 although a cleaning effect was obtained, no foaming was obtained due to the defoaming action of the organosiloxane derivative.
- Comparative Examples 7 to 11 using silicone oil (dimethicone), conventional silicone surfactant, hydrocarbon oil (liquid paraffin), and ester oil (cetyl trioctanoate) excellent foaming and cleaning effect are also obtained. A compatible cleaning charge was not obtained.
- Formulation Example 1 Make-up soap (compounding ingredient) (mass%) (1) Compound 1 2 (2) Ethanol 10 (3) Glycerin 10 (4) Diglycerin 3 (5) Sorbit liquid 8 (6) Isostearic acid 2 (7) Stearic acid 5 (8) Myristic acid 15 (9) Palmitic acid 3 (10) Polyoxyethylene (25) 3 Polyoxypropylene glycol (30) (11) Sodium palm oil fatty acid methyl taurine sodium 0.1 (12) 2-alkyl-N-carboxymethyl-N-2 Hydroxyethyl imidazolinium betaine (13) Palm oil fatty acid amidopropyl betaine 2 (14) Polydimethyldimethylmethylenepiperidinium 0.5 (15) Titanium oxide 0.1 (16) Sodium hydroxide solution (48%) 7 (17) Potassium hydroxide solution (47%) 3 (18)
- Formulation Example 3 Makeup Remover Foam (Compounding ingredient) (mass%) (1) Compound 3 3 (2) Glycerin 6 (3) Dipropylene glycol 4 (4) Isostearic acid 2 (5) Lauric acid 8 (6) Myristic acid 5 (7) Polyethylene glycol diisostearate 4 (8) Palm oil fatty acid diethanolamide 2.5 (9) Palm oil fatty acid sarcosine triethanolamine 10 (10) 2-alkyl-N-carboxymethyl-N-13 Hydroxyethylimidazolinium betaine (11) Polydimethylmethylenepiperidinium chloride solution 0.5 (12) Triethanolamine 12.4 (13) Sodium chloride 0.5 (14) Dibutylhydroxytoluene appropriate amount (15) edetate trisodium appropriate amount (16) purified water residue (17) perfume appropriate amount (Production method) (1) to (11) and (13) to (16) are all added and dissolved at 75 degrees. After dissolution, neutralize at (12), add (17) at the end, and then rapidly cool to 25 ° C. to obtain this
- Formulation Example 4 Makeup Remover Foam (Compounding ingredient) (mass%) (1) Compound 4 3 (2) Glycerin 25 (3) Sorbit liquid (70%) 5 (4) Polyethylene glycol 1500 10 (5) White beeswax 1 (6) Stearic acid 9 (7) Lauric acid 4 (8) Myristic acid 10 (9) Polyoxyethylene (25) 2 Polyoxypropylene glycol (30) (10) Polyoxyethylene glyceryl isostearate 2 (11) Self-emulsifying glyceryl monostearate 2 (12) Palm oil fatty acid methyl taurine sodium 1.5 (13) Lauryldimethylaminoacetic acid betaine 1 (14) Talc 0.1 (15) Potassium hydroxide 4 (16) Button extract 0.1 (17) Melissa extract 0.1 (18) edetate trisodium appropriate amount (19) ethyl cellulose appropriate amount (20) polyethylene powder 3 (21) Purified water Residue (22) Perfume appropriate amount (production method) (1) to (14) and (16) to (21) are all added and dissolved at 75 degrees
- Formulation Example 5 Hair wax remover shampoo (1) Compound 1 sodium salt 3 (2) Glycerin 3 (3) Polyoxyethylene lauryl ether (12EO) 1 (4) Palm oil fatty acid diethanolamide 3 (5) Palm oil fatty acid methyl taurine sodium 15 (6) Lauryldimethylaminoacetic acid betaine 4 (7) Polymer JR-400 (Amacor) 0.6 (8) Citric acid 0.25 (9) Sodium monohydrogen phosphate 0.1 (10) Iris root extract 0.02 (11) Sodium benzoate appropriate amount (12) Edetate disodium appropriate amount (13) Water residue (14) Fragrance appropriate amount (production method) (1) to (6) and (8) to (13) are all added and dissolved at 60 degrees. After dissolution, add (7) and stir well. Finally, add (14), and then rapidly cool to 25 ° C. to obtain this product.
- Formulation Example 6 Hair wax remover shampoo (compounding ingredient) (mass%) (1) Compound 2 sodium salt 3 (2) Ethylene glycol distearate 1.5 (3) Palm oil fatty acid ethanolamide 5.5 (4) Palm oil fatty acid methyl taurine sodium 8 (5) Palm oil fatty acid amidopropyl betaine 5 (6) Polymer JR-400 (Amacol) 0.5 (7) Citric acid 0.5 (8) Sodium chloride 1.2 (9) Loquat leaf extract 0.1 (10) Phenoxyethanol 0.1 (11) Sodium benzoate appropriate amount (12) Edetate disodium appropriate amount (13) Purified water Residue (14) Fragrance appropriate amount (Production method) (1) to (5) and (7) to (13) are all added and dissolved at 60 degrees. After dissolution, add (6) and stir well. Finally, add (14), and then cool rapidly to 25 ° C. to obtain this product.
- Compound 2 sodium salt 3 (2) Ethylene glycol distearate 1.5 (3) Palm oil fatty acid ethanolamide 5.5 (4) Palm oil fatty acid
Abstract
Description
を含有することを特徴とするものである。
また、前記洗浄料において、アニオン性界面活性剤が、脂肪酸石ケン、アシルメチルタウリン塩、及びアルキルエーテルカルボン酸塩の1種以上であることが好適である。
本発明にかかる洗浄料は、カルボキシル基を含む特定構造のオルガノシロキサン誘導体塩と、脂肪酸石ケン等のアニオン性界面活性剤とを含有することを特徴とするものである。
本発明に用いられるオルガノシロキサン誘導体は、一般式(1)又は一般式(3)で表される化合物である。
最初に、下記一般式(1)で表されるオルガノシロキサン誘導体について説明する。
上記一般式(1)において、R1~R3は、少なくとも1つが-O-Si(R4)3で表される官能基(R4は、炭素数1~6のアルキル基又はフェニル基のいずれかである)、又は-O-Si(R5)2-X1で表される官能基(R5は、炭素数1~6のアルキル基又はフェニル基のいずれかであり、X1はi=1のときの下記一般式(2)で示される官能基である)である。なお、R1~R3において、その全てが前記官能基のいずれかであってもよい。あるいは、R1~R3の少なくとも1つが前記官能基であれば、その他のR1~R3は、同一または異なっていてもよい置換又は非置換の一価炭化水素基のいずれかであってもよい。
すなわち、デンドリマー構造の階層nが1である場合、式(2)のシリルアルキル基は、
R1R2R3Si-(CH2)2-COOM (1-A)
HSi(-O-SiR2H)fRL 3-f
(式中、Rは炭素原子数1~6のアルキル基またはフェニル基のいずれかであり、RLは同一又は異なっていてもよい置換又は非置換の一価炭化水素基であり、fは1~3の整数である)で示されるジメチルシロキシ基を有するオルガノシランと、CH=CH2-A-COOSiMe3で示されるビニル末端を有するカルボン酸トリメチルシリル誘導体(式中、Aは前記同様の基)とを、白金系遷移金属触媒の存在下に付加反応させ、下基一般式の中間体(1-1)を得る工程。
Si(-O-SiR2H)fRL 3-f-(CH2)2-A-COOSiMe3 (1-1)
RBSi(O-R6)ai(OSiR7R8-Xi+1)3-ai
(式中、RBはCrH2rで表される直鎖状または分岐鎖状のアルケニル基であり、rは2~20の整数である。R6、R7、R8、Xi+1、aiは前記同様の基および数である)で示されるアルケニル基を有するオルガノシランとを、白金系触媒の存在下に付加反応させ、下記一般式の中間体(1-2)を得る工程。
Si{-O-SiR2-B-Si(O-R6)ai(OSiR7R8-Xi+1)3-ai}fRL 3-f-(CH2)2-A-COOSiMe3 (1-2)
中間体(1-2)に、保護基であるトリメチルシリル基1モルあたり、少なくとも1モル以上のメタノール等の一価アルコール、水又はこれらの混合物を加えて加熱することにより、加アルコール分解により脱保護させる工程。
金属イオン(Mn+)を含む化合物又は塩基性の有機化合物により中和する工程。
中和工程の一例として、水酸化ナトリウム(NaOH)、水酸化カリウム(KOH)、トリエタノールアミン、アルギニン、アミノメチルプロパノール(AMP)等の水溶液を添加することにより、カルボキシル基(-COOH)を中和する工程である。
上記一般式(3)において、式中、R9~R12は、同一又は異なっていてもよい置換又は非置換の一価炭化水素基のいずれかから選択される。R9~R12である非置換の一価炭化水素基は、メチル基、エチル基、プロピル基、ブチル基、ペンチル基、ヘキシル基、ヘプチル基、オクチル基、デシル基、ドデシル基等の直鎖状または分岐鎖状のアルキル基;アリル基、ヘキセニル基等の直鎖状または分岐鎖状のアルケニル基;シクロペンチル基、シクロヘキシル基等のシクロアルキル基;フェニル基、トリル基、ナフチル基等のアリール基;ベンジル基、フェニルエチル基、フェニルプロピル基、ナフチルメチル基、ナフチルエチル基等のアラルキル基が例示される。R9~R12である置換の一価炭化水素基は、これらの基の炭素原子に結合した水素原子が部分的に水酸基、ハロゲン原子、エポキシ基、アミノ基、メタクリル基、メルカプト基、アルコキシ基、ポリエーテル基またはパーフルオロポリエーテル基等の有機基で置換された基であり、3,3,3-トリフロロプロピル基、3,3,4,4,4-ペンタフロロブチル基等のパーフルオロアルキル基;3-アミノプロピル基、3-(アミノエチル)アミノプロピル基等のアミノアルキル基;アセチルアミノアルキル基等のアミドアルキル基が例示される。R9~R12は炭素数1~20のアルキル基、アリール基およびアラルキル基であることが好ましく、1分子中のR9~R12の90モル%以上がメチル基及び/またはフェニル基であることが特に好ましい。
MOOC-(CH2)2-(SiR9R10-O)p-SiR11R12-(CH2)2-COOM (3-A)
H-(SiR9R10-O)p-SiR11R12-H
(式中、R9~R12、p、qは前記同様の基)
で示される分子鎖両末端にケイ素原子結合水素原子を有するオルガノハイドロジェンポリシロキサン1モルに対し、少なくとも2モルのCH=CH2-Q-COOSiMe3で示されるビニル末端を有するカルボン酸トリメチルシリル誘導体とを、白金系触媒の存在下に付加反応させ、保護基であるトリメチルシリル基1モルあたり、少なくとも1モル以上のメタノール等の一価アルコール、水又はこれらの混合物を加えて加熱することにより、加アルコール分解により脱保護し、さらに対応する金属イオン(Mn+)を含む化合物又は塩基性の有機化合物による中和を行うことによって製造することができる。なお、Qは前記同様の基である。中和工程に用いる金属イオン含有化合物又は塩基性有機化合物としては、前記同様の化合物を例示することができる。
また、上記一般式(1’)又は上記一般式(3’)で表されるオルガノシロキサン誘導体は、該オルガノシロキサン誘導体とともに、金属イオン含有化合物又は塩基性有機化合物を洗浄料中に配合することで、本発明にかかる洗浄料として用いることができる。すなわち、本発明においては、洗浄料処方中で、オルガノシロキサン誘導体の末端カルボキシル基が金属塩あるいは有機塩(すなわち、上記一般式(1)又は上記一般式(3)で表されるオルガノシロキサン誘導体)になり得る状態であればよいため、末端カルボキシル基であるオルガノシロキサン誘導体と、金属イオン含有化合物又は塩基性有機化合物とを、個別に洗浄料中に配合して用いることが可能である。
本発明に用いられるアニオン性界面活性剤は、炭素数10~20のアルキル基を有するカルボン酸塩、硫酸塩、スルホン酸塩、又はリン酸塩(以下、単に各種アニオン界面活性剤という場合がある)から選ばれるものである。これらの各種アニオン性界面活性剤は、飽和又は不飽和のアルキル基を有する各種酸の塩であり、アルキル鎖は直鎖状、分岐状のいずれであっても構わない。また、前記アルキル鎖のほかに他の官能基(例えば、アミノ基、エーテル基等)あるいは鎖状構造(例えば、ポリオキシアルキレン基等)を有していてもよい。なお、本発明においては、前記各種酸が予め塩を形成した状態で洗浄料中に配合していてもよく、あるいは前記各種酸と、塩を形成するための塩基性物質とをそれぞれ個別に洗浄料中に配合し、処方内で塩を形成してもよい。例えば、アルキルカルボン酸と水酸化カリウムとを個別に洗浄料処方中に添加することにより、処方内での中和反応によってアルキルカルボン酸カリウム塩が形成される。なお、各種酸との中和により塩を形成する塩基性物質としては、例えば、水酸化カリウム、水酸化ナトリウム等のアルカリ金属類の水酸化物、2-アミノ-2-メチル-1-プロパノール、2-アミノ-2-メチル-1,3-プロパンジオール、トリエタノールアミン、ジエタノールアミン、モノエタノールアミン、トリイソプロパノールアミン、2-アミノ-2-ヒドロキシメチル-1,3-プロパンジオール、L-アルギニン、L-リジン、モルホリン、N-アルキルタウリン塩等の塩基性窒素含有化合物が挙げられる。
以下に実施例及び比較例において用いたオルガノシロキサン誘導体(化合物1~4,比較化合物1~4)の構造及びその合成方法を示す。なお、各化合物は1H,13C,29Si-NMR(NMR装置:Fourier Transform Nuclear Magnetic Resonance Spectrometer JEOL JNM-EX400(日本電子社製)により同定した。
撹拌機、還流冷却器、滴下ロート及び温度計を備えたフラスコに1,1,1,3,5,5,5-ヘプタメチルトリシロキサン100g、白金-1,3-ジビニル-1,1,3,3-テトラメチルジシロキサン錯体のトルエン溶液0.02gを加え、70-100℃の範囲を保つように、ウンデシレン酸トリメチルシリル105gを滴下した。滴下終了後、2時間、100℃で熟成した後、ガスクロマトグラフィーを用いて反応の完了を確認した。低沸点分を減圧下、留去した。その後、メタノール、水を加え、還流下5時間熟成し、脱保護を行った。その後再び低沸点分を減圧下除去し、化合物1を得た。分析の結果、上記化学構造式で示される化合物1であることが確認された。
撹拌装置、温度計、還流冷却管、滴下ロートを取り付けたフラスコに、テトラキス(ジメチルシロキシ)シラン100gと白金-1,3-ジビニル-1,1,3,3-テトラメチルジシロキサン錯体のトルエン溶液0.02gを投入し、これらを撹拌しながら90℃に加熱した。次いでこれに、ウンデシレン酸トリメチルシリル15.6gを、滴下ロートを用いて反応温度が90℃を保つようにゆっくり滴下した。滴下終了後、反応溶液を100℃で1時間加熱した。冷却後、減圧蒸留したところ、35.3gの無色透明液体が得られた。分析の結果、この液体は下記構造式で示される化合物であることが確認された。これを中間体2Aとした。
撹拌機、還流冷却器、滴下ロート及び温度計を備えたフラスコにウンデシレン酸トリメチルシリル460.81g,白金-1,3-ジビニル-1,1,3,3-テトラメチルジシロキサン錯体のトルエン溶液0.05gを加え、70-80℃の範囲を保つように、1, 1,3,3-テトラメチルジシロキサン100gを滴下した。滴下終了後、2時間、100℃で熟成した後、ガスクロマトグラフィーを用いて反応の完了を確認した。低沸点分を減圧下、留去した。その後、メタノール240gを加え、還流下5時間熟成し、脱保護を行った。その後再び低沸点分を減圧下除去し、化合物3を得た。分析の結果、上記化学構造式で示される化合物3であることが確認された。
撹拌機、還流冷却器、滴下ロート及び温度計を備えたフラスコにウンデシレン酸トリメチルシリル225.0g,白金-1,3-ジビニル-1,1,3,3-テトラメチルジシロキサン錯体のトルエン溶液0.05gを加え、70-80℃の範囲を保つように、下記一般式で表される両末端Si-Hシロキサン225gを滴下した。
各実施例及び比較例の組成物について、専門パネル10名による洗浄を行い、泡立ち、メーク落ち、ヘアワックスの落ちの各項目について官能評価を行った。評価は、以下に示すように各項目ごとに5段階(1~5点)の評価点方式により行い、10名の平均点を算出し、下記判定基準により評価した。
(判定基準)
◎:非常に良好(平均点が4.5点以上)
○:良好(平均点が3.5点以上4.5未満)
△:普通(平均点が2.5点以上3.5点未満)
×:不良(平均点が2.5点未満)
(評価点基準)
5点:泡立ちが良い(泡の量が多い)
4点:泡立ちがやや良い(泡の量がやや多い)
3点:普通
2点:泡立ちがやや悪い(泡の量がやや少ない)
1点:泡立ちが悪い(泡の量が少ない)
メーク落ち
(評価点基準)
5点:メークの落ちがよい
4点:ややメークの落ちがよい
3点:普通
2点:ややメークの落ちが悪い
1点:メークの落ちが悪い
ヘアワックスの落ち
(評価点基準)
5点:ヘアワックスの落ちがよい
4点:ややヘアワックスの落ちがよい
3点:普通
2点:ややヘアワックスが悪い
1点:ヘアワックスの落ちが悪い
ファンデーション:マキアージュ フローレンス スキンリキッド UV(資生堂)
口紅:マキアージュ カラーオン クライマックスルージュ RD350(資生堂)
マスカラ:マキアージュ マスカラコーミンググラマー(資生堂)
ヘアワックス:UNO ツーウェイスーパーワックス(資生堂)
処方例1:メーク落とし石鹸
(配合成分) (質量%)
(1)化合物1 2
(2)エタノール 10
(3)グリセリン 10
(4)ジグリセリン 3
(5)ソルビット液 8
(6)イソステアリン酸 2
(7)ステアリン酸 5
(8)ミリスチン酸 15
(9)パルミチン酸 3
(10)ポリオキシエチレン(25) 3
ポリオキシプロピレングリコール(30)
(11)ヤシ油脂肪酸メチルタウリンナトリウム 0.1
(12)2-アルキル-N-カルボキシメチル-N- 2
ヒドロキシエチルイミダゾリニウムベタイン
(13)ヤシ油脂肪酸アミドプロピルベタイン 2
(14)ポリ塩化ジメチルメチレンピペリジニウム 0.5
(15)酸化チタン 0.1
(16)水酸化ナトリウム液(48%) 7
(17)水酸化カリウム液(47%) 3
(18)塩化ナトリウム 0.1
(19)メタリン酸ナトリウム 0.1
(20)グリチルリチン酸ジカリウム 0.05
(21)ヒドロキシエタンジホスホン酸4ナトリウム(30%) 適量
(22)エチレンジアミンヒドロキシエチル三酢酸三ナトリウム 適量
(23)白糖 10
(24)精製水 残余
(製造方法)
(24)中に(10)から(14)、(18)から(23)を加え溶解させる。ついで(1)から(9)を加えて75度で溶解させ、(16),(17)を加えて中和させる。容器に充填し、冷却し固形石けんを得る。
(配合成分) (質量%)
(1)化合物2 4
(2)エタノール 15
(3)ソルビット液 10
(4)ポリオキシプロピレン(9)ジグリセリルエーテル 4
(5)ヒマシ油 2
(6)イソステアリン酸 2
(7)ステアリン酸 7
(8)ラウリン酸 6
(9)ミリスチン酸 11
(10)パルミチン酸 3
(11)ドデカン-1,2-ジオール酢酸エーテルナトリウム 3
(12)N-メチルタウリンナトリウム 5
(13)水酸化ナトリウム 4
(14)塩化ナトリウム 0.5
(15)カモミラエキス 0.1
(16)ジブチルヒドロキシトルエン 適量
(17)ヒドロキシエタンジホスホン酸4ナトリウム(30%) 0.1
(18)エデト酸3ナトリウム 0.1
(19)4-tert-ブチル-4’- 0.05
メトキシジベンゾイルメタン
(20)パラメトキシケイヒ酸2-エチルヘキシル 0.05
(21)白糖・ソルビット混合物 15
(22)色素 適量
(23)精製水 残余
(24)香料 適量
(製造方法)
(1)~(12)、(14)~(23)をすべて加えて75度で溶解させる。溶解後(13)で中和し、最後に(24)を加えて、その後25℃まで急冷し本品を得る。
(配合成分) (質量%)
(1)化合物3 3
(2)グリセリン 6
(3)ジプロピレングリコール 4
(4)イソステアリン酸 2
(5)ラウリン酸 8
(6)ミリスチン酸 5
(7)ジイソステアリン酸ポリエチレングリコール 4
(8)ヤシ油脂肪酸ジエタノールアミド 2.5
(9)ヤシ油脂肪酸サルコシントリエタノールアミン 10
(10)2-アルキル-N-カルボキシメチル-N- 13
ヒドロキシエチルイミダゾリニウムベタイン
(11)ポリ塩化ジメチルメチレンピペリジニウム液 0.5
(12)トリエタノールアミン 12.4
(13)塩化ナトリウム 0.5
(14)ジブチルヒドロキシトルエン 適量
(15)エデト酸3ナトリウム 適量
(16)精製水 残余
(17)香料 適量
(製造方法)
(1)~(11)、(13)~(16)をすべて加えて75度で溶解させる。溶解後(12)で中和し、最後に(17)を加えて、その後25℃まで急冷し本品を得る。
(配合成分) (質量%)
(1)化合物4 3
(2)グリセリン 25
(3)ソルビット液(70%) 5
(4)ポリエチレングリコール1500 10
(5)サラシミツロウ 1
(6)ステアリン酸 9
(7)ラウリン酸 4
(8)ミリスチン酸 10
(9)ポリオキシエチレン(25) 2
ポリオキシプロピレングリコール(30)
(10)イソステアリン酸ポリオキシエチレングリセリル 2
(11)自己乳化型モノステアリン酸グリセリン 2
(12)ヤシ油脂肪酸メチルタウリンナトリウム 1.5
(13)ラウリルジメチルアミノ酢酸ベタイン 1
(14)タルク 0.1
(15)水酸化カリウム 4
(16)ボタンエキス 0.1
(17)メリッサエキス 0.1
(18)エデト酸3ナトリウム 適量
(19)エチルセルロース 適量
(20)ポリエチレン末 3
(21)精製水 残余
(22)香料 適量
(製造方法)
(1)~(14)、(16)~(21)をすべて加えて75度で溶解させる。溶解後(15)で中和し、最後に(22)を加えて、その後25℃まで急冷し本品を得る。
(1)化合物1ナトリウム塩 3
(2)グリセリン 3
(3)ポリオキシエチレンラウリルエーテル(12EO) 1
(4)ヤシ油脂肪酸ジエタノールアミド 3
(5)ヤシ油脂肪酸メチルタウリンナトリウム 15
(6)ラウリルジメチルアミノ酢酸ベタイン 4
(7)ポリマーJR-400(アマコール社製) 0.6
(8)クエン酸 0.25
(9)無水リン酸1水素ナトリウム 0.1
(10)イリス根エキス 0.02
(11)安息香酸ナトリウム 適量
(12)エデト酸2ナトリウム 適量
(13)水 残余
(14)香料 適量
(製造方法)
(1)~(6)、(8)~(13)をすべて加えて60度で溶解させる。溶解後(7)を加えて十分攪拌する、最後に(14)を加えて、その後25℃まで急冷し本品を得る。
(配合成分) (質量%)
(1)化合物2ナトリウム塩 3
(2)ジステアリン酸エチレングリコール 1.5
(3)ヤシ油脂肪酸エタノールアミド 5.5
(4)ヤシ油脂肪酸メチルタウリンナトリウム 8
(5)ヤシ油脂肪酸アミドプロピルベタイン 5
(6)ポリマーJR-400(アマコール社製) 0.5
(7)クエン酸 0.5
(8)塩化ナトリウム 1.2
(9)ビワ葉エキス 0.1
(10)フェノキシエタノール 0.1
(11)安息香酸ナトリウム 適量
(12)エデト酸2ナトリウム 適量
(13)精製水 残余
(14)香料 適量
(製造方法)
(1)~(5)、(7)~(13)をすべて加えて60度で溶解させる。溶解後(6)を加えて十分攪拌する、最後に(14)を加えて、その後25℃まで急冷し本品を得る。
Claims (5)
- 下記一般式(1)又は下記一般式(3)で表されるオルガノシロキサン誘導体塩と、
炭素数10~20のアルキル基を有するカルボン酸塩、硫酸塩、スルホン酸塩、又はリン酸塩から選ばれる1種以上のアニオン性界面活性剤と
を含有する洗浄料。
- 請求項1に記載の洗浄料において、オルガノシロキサン誘導体塩が、上記一般式(1)で表され、R1及びR2が-O-Si(R4)3で表される官能基(R4は、炭素数1~6のアルキル基である)であり、R3が炭素数1~10の1価炭化水素基であり、qが6~20の整数であることを特徴とする洗浄料。
- 請求項1に記載の洗浄料において、オルガノシロキサン誘導体塩が、上記一般式(3)で表され、R9~R12が置換または非置換の炭素原子数1~20のアルキル基、アリール基及びアラルキル基からなる群から選択される基であり、qが6~20の整数であり、pが1~20の数であることを特徴とする洗浄料。
- 請求項1から4のいずれかに記載の洗浄料において、アニオン性界面活性剤が、脂肪酸石ケン、アシルメチルタウリン塩、及びアルキルエーテルカルボン酸塩の1種以上であることを特徴とする洗浄料。
Priority Applications (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP09708011A EP2251403B1 (en) | 2008-02-05 | 2009-01-30 | Cleansing composition |
US12/866,286 US8513174B2 (en) | 2008-02-05 | 2009-01-30 | Cleanser |
ES09708011T ES2394410T3 (es) | 2008-02-05 | 2009-01-30 | Composición limpiadora |
CN200980104315.8A CN101939406B (zh) | 2008-02-05 | 2009-01-30 | 清洁产品 |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2008025060A JP5305677B2 (ja) | 2008-02-05 | 2008-02-05 | 洗浄料 |
JP2008-025060 | 2008-02-05 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2009099007A1 true WO2009099007A1 (ja) | 2009-08-13 |
Family
ID=40952082
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/JP2009/051571 WO2009099007A1 (ja) | 2008-02-05 | 2009-01-30 | 洗浄料 |
Country Status (8)
Country | Link |
---|---|
US (1) | US8513174B2 (ja) |
EP (1) | EP2251403B1 (ja) |
JP (1) | JP5305677B2 (ja) |
KR (1) | KR101578957B1 (ja) |
CN (1) | CN101939406B (ja) |
ES (1) | ES2394410T3 (ja) |
TW (1) | TWI457143B (ja) |
WO (1) | WO2009099007A1 (ja) |
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JP2013185063A (ja) * | 2012-03-07 | 2013-09-19 | Kao Corp | 洗浄剤組成物の製造方法 |
WO2014069400A1 (ja) * | 2012-10-30 | 2014-05-08 | 株式会社 資生堂 | オルガノシロキサン誘導体組成物 |
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EP3530722B1 (en) * | 2016-10-19 | 2022-11-16 | Shiseido Company, Ltd. | Detergent composition |
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US11793744B2 (en) | 2017-08-25 | 2023-10-24 | Coty, Inc. | Cosmetic products including bis-carboxy silicone polymer component |
WO2020208838A1 (ja) | 2019-04-10 | 2020-10-15 | ダウ・東レ株式会社 | 水中油型クレンジング化粧料 |
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Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2013173807A (ja) * | 2012-01-25 | 2013-09-05 | P & P F:Kk | 固形石鹸 |
JP2013185063A (ja) * | 2012-03-07 | 2013-09-19 | Kao Corp | 洗浄剤組成物の製造方法 |
WO2014069400A1 (ja) * | 2012-10-30 | 2014-05-08 | 株式会社 資生堂 | オルガノシロキサン誘導体組成物 |
JP2014088344A (ja) * | 2012-10-30 | 2014-05-15 | Shiseido Co Ltd | オルガノシロキサン誘導体組成物 |
Also Published As
Publication number | Publication date |
---|---|
CN101939406A (zh) | 2011-01-05 |
EP2251403A4 (en) | 2011-11-09 |
EP2251403B1 (en) | 2012-08-29 |
US8513174B2 (en) | 2013-08-20 |
CN101939406B (zh) | 2014-06-11 |
JP5305677B2 (ja) | 2013-10-02 |
KR20100118578A (ko) | 2010-11-05 |
EP2251403A1 (en) | 2010-11-17 |
ES2394410T3 (es) | 2013-01-31 |
KR101578957B1 (ko) | 2015-12-18 |
TWI457143B (zh) | 2014-10-21 |
JP2009185144A (ja) | 2009-08-20 |
TW200938230A (en) | 2009-09-16 |
US20100317555A1 (en) | 2010-12-16 |
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