WO2007116586A1 - Cleansing composition - Google Patents

Cleansing composition Download PDF

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Publication number
WO2007116586A1
WO2007116586A1 PCT/JP2007/000375 JP2007000375W WO2007116586A1 WO 2007116586 A1 WO2007116586 A1 WO 2007116586A1 JP 2007000375 W JP2007000375 W JP 2007000375W WO 2007116586 A1 WO2007116586 A1 WO 2007116586A1
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WO
WIPO (PCT)
Prior art keywords
component
cleaning composition
composition according
weight
general formula
Prior art date
Application number
PCT/JP2007/000375
Other languages
French (fr)
Japanese (ja)
Inventor
Ryosuke Fujii
Yoshinori Tamura
Original Assignee
Kao Corporation
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Filing date
Publication date
Application filed by Kao Corporation filed Critical Kao Corporation
Priority to KR1020087024421A priority Critical patent/KR101453106B1/en
Priority to CN2007800125486A priority patent/CN101415401B/en
Priority to JP2008509698A priority patent/JP5101493B2/en
Publication of WO2007116586A1 publication Critical patent/WO2007116586A1/en

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Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/55Phosphorus compounds
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/66Non-ionic compounds
    • C11D1/83Mixtures of non-ionic with anionic compounds
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/33Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • A61K8/39Derivatives containing from 2 to 10 oxyalkylene groups
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/46Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing sulfur
    • A61K8/463Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing sulfur containing sulfuric acid derivatives, e.g. sodium lauryl sulfate
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/55Phosphorus compounds
    • A61K8/556Derivatives containing from 2 to 10 oxyalkylene groups
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/72Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/84Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions otherwise than those involving only carbon-carbon unsaturated bonds
    • A61K8/86Polyethers
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q19/00Preparations for care of the skin
    • A61Q19/10Washing or bathing preparations
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/02Anionic compounds
    • C11D1/34Derivatives of acids of phosphorus
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2800/00Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
    • A61K2800/40Chemical, physico-chemical or functional or structural properties of particular ingredients
    • A61K2800/59Mixtures
    • A61K2800/596Mixtures of surface active compounds
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/02Anionic compounds
    • C11D1/12Sulfonic acids or sulfuric acid esters; Salts thereof
    • C11D1/29Sulfates of polyoxyalkylene ethers
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/02Anionic compounds
    • C11D1/34Derivatives of acids of phosphorus
    • C11D1/342Phosphonates; Phosphinates or phosphonites
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/66Non-ionic compounds
    • C11D1/722Ethers of polyoxyalkylene glycols having mixed oxyalkylene groups; Polyalkoxylated fatty alcohols or polyalkoxylated alkylaryl alcohols with mixed oxyalkylele groups

Definitions

  • the present invention relates to a detergent composition having little irritation to skin and the like, excellent foaming properties, creamy quality, and good rinsing properties.
  • sulfate surfactants such as alkyl sulfates and polyoxyethylene alkyl sulfates have been widely used as surfactants for cleaning agents.
  • sulfate-based surfactants are not suitable as a cleaning agent for the body because they are light and rough in foam quality, and are not easily rinsed and rinsed.
  • phosphate ester surfactants are known as mild surfactants with low irritation to the skin, etc., but any of them is a mixture of monoester and diester or mono, di, tri. Since it was a mixture of esters, it was poor in solubility in water and foaming power. When this was used alone as a main component of a cleaning agent, there was generally a problem in foaming power.
  • Patent Document 1 Japanese Laid-Open Patent Publication No. 2 2003-3 1 3 5 8 5
  • Patent Document 2 Japanese Patent Laid-Open No. 2 0 0 6 _ 2 2 1 1 6
  • Patent Document 3 Japanese Patent Laid-Open No. 2 0 0 5 _ 2 0 6 8 0 4
  • R 1 , R 2 and R 3 each represent a linear or branched alkyl group or alkenyl group having 8 to 18 carbon atoms, and X 1 , X 2 and Y represent a hydrogen atom and an alkali, respectively.
  • a metal atom, an alkaline earth metal atom, an alkanolamine, or an ammonium salt, and the average number of moles added, k, m, and n are each 0 to 10.
  • R 4 represents an alkyl group or alkenyl group having 8 to 18 carbon atoms
  • M represents an alkali metal atom, an alkaline earth metal atom, an alkanolamine, an ammonium or a basic amino acid, and an average addition.
  • Mole number p shows the number of 0-5.
  • (C) (C-1) a linear or branched alkyl group having 6 to 12 carbon atoms, wherein ⁇ is one or more glyceryl ethers having an alkenyl group, and
  • R 5 represents a linear or branched alkyl group or alkyl group having 6 to 10 carbon atoms
  • R 6 represents a hydrogen atom or a methyl group
  • AO represents 2 to 4 carbon atoms.
  • the average number of added moles q is a number of 0.5 to 3.
  • the cleaning composition containing this is provided.
  • the present invention also provides a method for cleaning the body by applying the cleaning composition to the body.
  • the present invention provides use of the cleaning composition for body cleaning.
  • An object of the present invention is to provide a detergent composition that is less irritating to the skin and the like, is excellent in foaming properties, has a foam quality of creamy, and has good rinsing properties.
  • the cleaning composition of the present invention is less irritating to the skin and the like, has excellent foaming properties, has a creamy quality, and has good rinsing properties.
  • R 1 , R 2 and R 3 are each a carbon number It is preferably an alkyl group of 10 to 16, more preferably 12 to 14 , and X 1 , X 2 and Y are preferably an alkali metal atom such as gallium or sodium, or triethanolami, particularly Potassium is preferable from the viewpoint of solubility in water.
  • the average number of moles of ethylene oxide added k, m and n is preferably 0 to 4 moles, more preferably 0 to 2 and even more preferably 0 to 1 mole from the viewpoint of foaming power.
  • the content of the phosphoric acid ester-based surfactant of component (A) is foaming, detergency and And 1 to 15% by weight of the cleaning composition of the present invention is preferable, 2 to 10% by weight is more preferable, and 3 to 10% by weight is still more preferable.
  • Component (A) is, for example, an ethylene oxide added to a corresponding aliphatic alcohol or a corresponding aliphatic alcohol to obtain an ethoxylate having an average addition mole number of more than 0 to 10; phosphoric anhydride; Phosphoric acid ester obtained by reacting phosphoric acid such as orthophosphoric acid, polyphosphoric acid or oxyphosphoric acid, or the phosphoric acid ester partially or completely with sodium hydroxide, hydroxylated lithium, etc. It is a phosphoric ester salt obtained by neutralization.
  • a J / (a 2 ) can be controlled by the ratio between the aliphatic alcohol and the water contained in the phosphorylating agent.
  • R 4 has an average carbon number of 8 to 18, preferably 10 to 16 from the viewpoint of foamability. More preferably, they are 10 to 14 linear or branched alkyl groups or alkenyl groups.
  • M is preferably an alkali metal such as potassium or sodium, triethanolamine, or ammonium, and more preferably potassium, sodium, or ammonium from the viewpoint of solubility in water and foaming.
  • the content of the component (B) is preferably 5 to 40% by weight, more preferably 5 to 35% by weight, from the viewpoint of detergency and foaming property of the cleaning composition of the present invention, 20% by weight is even more preferred.
  • the glyceryl ether of the component (C-1) has a linear or branched alkyl group or alkenyl group having 6 to 12 carbon atoms, such as an n-hexyl group, an isohexyl group, Those having an alkyl group having 6 to 12 carbon atoms such as n-heptyl group, n-octyl group, 2_ethylhexyl group, n_nonyl group, n_decyl group, n_lauryl group, and the like are preferable. It is preferable to have 1 or 2 alkyl groups having 6 to 11 carbon atoms, 6 to 10 carbon atoms, especially 8 carbon atoms, and more preferably one.
  • One or more glyceryl ethers of component (C-1) can be used, and 0.1 to 20% by weight, further 0.1 to 10% by weight, and further 0.1 to 5% by weight in the total composition.
  • % Is preferable in terms of rinsing properties and foaming power.
  • the component (C_1) can be obtained, for example, by hydrolyzing the corresponding glycidyl ether and water at 100 to 230 ° C.
  • R 5 is a linear or branched chain having 6 to 10 carbon atoms, preferably 8 to 10 carbon atoms. And an alkyl group having 8 carbon atoms is preferred.
  • AO is an alkyleneoxy group having 2 to 4 carbon atoms, more preferably an alkyleneoxy group having 2 to 3 carbon atoms, and still more preferably an alkyleneoxy group having 3 carbon atoms. Specific examples include an ethyleneoxy group, a propyleneoxy group, and a butyleneoxy group. An ethyleneoxy group and a propyleneoxy group are preferable, and a propyleneoxy group is more preferable.
  • the average added mole number q represents a number of 0.5 to 3, preferably 1 to 3, and more preferably 2 to 3.
  • AO max is the total component (C _ 2) from the viewpoint of economy that reduces the burden of manufacturing costs such as refining. 70% by weight or less is preferable, 60% by weight More preferably, it is more preferably 50% by weight or less.
  • AO max is 60% by weight or less, further 50% by weight or less, and further 40% by weight or less of the total component (C_2). preferable.
  • AO max is 70% by weight or less, further 60% by weight or less, and further 50% by weight of the total component (C-2). % Or less is preferable.
  • R 6 represents a hydrogen atom or a methyl group, more preferably a hydrogen atom.
  • One or more components (C_ 2) can be used, and the total composition is 0.1 to 20% by weight, further 0.1 to 15% by weight 0 / o, and further 0.1 to 10% by weight. It is preferable to blend them in terms of rinsing properties and foaming power.
  • the component (C_2) can be obtained, for example, by reacting propylene oxide and / or ethylene oxide with the corresponding aliphatic alcohol and then distilling the raw material alcohol.
  • the total amount of component (C) is preferably 0.1 to 20% by weight, more preferably 0.1 to 15% by weight, more preferably 0.1 to 10% by weight in the cleaning composition of the present invention. Even more preferable.
  • the cleaning composition of the present invention is a cleaning composition useful as a skin cleaning agent such as a facial cleanser, a shampoo, a body shampoo, or a body cleaner such as a hair cleaner. It is preferably used as a skin cleanser such as body shampoo.
  • These cleaning compositions can contain optional components depending on the purpose.
  • optional components include other anionic surfactants, nonionic surfactants, amphoteric surfactants, force thionic surfactants, and conditioning components that are usually blended in these detergents. .
  • anionic surfactants include fatty acid salts, sulfosuccinic acid surfactants, sulfosuccinamate surfactants, polyoxyalkylene alkylamide ether sulfates, monoglyceride sulfates, and olefin sulfones. Acid salts, alkane sulfonates, acylated isethionates, acylated amino acid salts, polyoxyalkylene alkyl ether phosphates other than the component (A), etc.
  • nonionic surfactant examples include alkylpolydarcoside, sucrose fatty acid ester, polyglycerin fatty acid ester, fatty acid alcohol amide, alkylamine oxide, and fatty acid polyhydric alcohol ester.
  • cationic surfactants include linear or branched mono- or di-long chain alkyl quaternary ammonium salts, mono- or di-long chain alkyl tertiary amines, and the like.
  • Amide amino acid-based activator Carbobetaine-based activator, Sulfobetaine-based activator, Amidosulfobetaine-based activator, Imidazolinium betaine-based activator, Amino acid-based betaine-activator, Phosphobetaine-based activator Etc.
  • conditioning components include higher alcohols, silicone and silicone derivatives, lanolin, squalene, hydrocarbons, protein derivatives, polyethylene glycol fatty acid esters and other oil agents, cationized cellulose, cationized guagam and marcoat. (Naruco Co., Ltd.), Softcare KG-3301 W [manufactured by Kao Corporation], and the like.
  • water-soluble polymers such as polysaccharides such as methylcellulose, hydroxyethylcellulose, carboxyvinyl polymer, xanthan gum; polyoxyalkylene Viscosity modifiers such as sorbitan ester, polyoxyethylene glycol distearate, ethanol, etc .; Ethylenediamine tetraacetic acid (EDTA), phosphonates and other chelating agents; methylparaben, butylparaben and other preservatives; vitamins and precursors thereof Active ingredients of: Lecithin, animal and plant extracts such as gelatin or derivatives thereof; polymer fine powder such as Nai Nya polyethylene; anti-inflammatory agent such as dipotassium glycyrrhizinate; And anti-dandruff agents; Antioxidants such as dibutylhydroxytoluene; pearlizing agents, ultraviolet absorbers, pH adjusting agents, dyes, fragrances, and water can be
  • the detergent composition of the present invention preferably has a pH of 4-8.
  • the cleaning composition of the present invention is used with water having a hardness of 1 to 30 ° DH. Is preferred.
  • the water used here preferably has a pH of 4 to 9.
  • the cleaning composition of the present invention can be produced according to a conventional method. There are no particular limitations on the dosage form of the cleaning composition of the present invention, and various conventionally known dosage forms such as liquid body shampoos, cream facial cleansings, and the like can be used.
  • the cleaning composition of the present invention is particularly suitable as a cleaning agent for body such as skin and hair.
  • Add [P 2 0 5 ⁇ n H 2 0 and P 2 0 5 1 9.6 g (0.14 mol) H 2 0 1 2.3 g (0.68 mol)] to 35 ° C Stir and mix. Further, 62.1 g (0.43 mol) of phosphorus pentoxide (effective content 98.5% by weight) was gradually added over 60 minutes with stirring.
  • 2-Ethylhexyl glycidyl ether 208 g, water 104.8 g, laur 5.82 g of phosphoric acid and 18.5 g of potassium hydroxide were placed in an autoclave and stirred at 140 ° C. for 5 hours. After dehydration at 100 ° C under reduced pressure (6.67 k Pa), add 9.7 g of lauric acid and 2.72 g of potassium hydroxide, react at 160 ° C for 15 hours, and then distilled under reduced pressure (53-67 Pa, 120-123 ° C.), 2-ethylhexyl glyceryl ether shown in Table 1 was obtained.
  • 1-octanol (Calcoal 0898, manufactured by Kao Corporation) 1 61 5. 0 g (1 2. 35 mo I) and hydroxylated power of 6.9 g (0.12 mo I) were charged into the autoclave, After dehydration at 1 10 ° C and 13.3 kPa, addition reaction was carried out at 120 ° C while injecting 1434 g (24. 69 0 1) of propylene oxide at 0.3 MPa.
  • 1-octanol was distilled off from 1 000 g of the obtained filtrate under the conditions of 130 ° C. and 1.3 kPa. Further, steam treatment was performed by blowing 100 g of steam under the conditions of 145 ° C., 6. O k Pa, and 5 hours to obtain dipropylene glycol monooctyl ether shown in Table 1.
  • a cleaning composition having the composition shown in Table 1 was prepared by mixing each component at 70 ° C according to a conventional method (1 "1 was adjusted to 6-7), and 1 g of this was applied to the palm of the hand and arm. Foaming properties, foam quality and rinsing properties when washed were evaluated by 10 expert panelists according to the following evaluation criteria: Table 1 shows the results.
  • a face wash and whole body cleanser with a pH of 5.0-0.7.0 were prepared with the following formulation. pH was adjusted with citrate and potassium hydroxide. Both are hypoallergenic and the pH of the water used is less than 4-5, less than 5-8, and 8-9, and the hardness of the water used is 1-30 ° In all areas of DH, foaming was good, foam quality was creamy, and rinsing was good.

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Abstract

Disclosed is a cleansing composition which shows little irritation to the skin or the like, has excellent foamability, generate creamy foam, and has good rinsing properties. The cleansing composition comprises the following components (A), (B) and (C): (A) a phosphoric acid ester surfactant mixture of (a1) a phosphoric acid monoester surfactant represented by the general formula (1) and (a2) a phosphoric acid diester surfactant represented by the general formula (2), wherein the content ratio between the components [(a1)/(a2)] is 90/10 to 50/50 by weight;. (B) a sulfuric acid ester surfactant represented by the general formula (3); and (C) (C-1) at least one glyceryl ether having a linear or branched alkyl or alkenyl group having 6 to 12 carbon atoms and (C-2) at least one member selected from compounds represented by the general formula (4).

Description

明 細 書  Specification
洗浄剤組成物  Cleaning composition
技術分野  Technical field
[0001 ] 本発明は、 皮膚等に対する刺激が少なく、 起泡性に優れ、 泡質がクリーミ 一で、 かつすすぎ性が良好な洗浄剤組成物に関する。  [0001] The present invention relates to a detergent composition having little irritation to skin and the like, excellent foaming properties, creamy quality, and good rinsing properties.
背景技術  Background art
[0002] 従来、 洗浄剤用の界面活性剤として、 アルキル硫酸塩、 ポリオキシェチレ ンアルキル硫酸塩等の硫酸エステル系界面活性剤が広く用いられてきた。 し かし、 このような硫酸エステル系界面活性剤は泡質が軽く粗いことや、 すす ぎの際にぬるつき、 すすぎ性が悪いことから、 身体用の洗浄剤としては不適 であった。  Conventionally, sulfate surfactants such as alkyl sulfates and polyoxyethylene alkyl sulfates have been widely used as surfactants for cleaning agents. However, such sulfate-based surfactants are not suitable as a cleaning agent for the body because they are light and rough in foam quality, and are not easily rinsed and rinsed.
[0003] —方、 リン酸エステル系界面活性剤は、 皮膚等に対する刺激性が低くマイ ルドな界面活性剤として知られているが、 いずれもモノエステルとジエステ ルの混合物あるいはモノ、 ジ、 トリエステルの混合物であったため、 水に対 する溶解性及び泡力に劣り、 これを洗浄剤主成分として単独で用いたのでは 、 一般に起泡力に問題が有った。  [0003]-On the other hand, phosphate ester surfactants are known as mild surfactants with low irritation to the skin, etc., but any of them is a mixture of monoester and diester or mono, di, tri. Since it was a mixture of esters, it was poor in solubility in water and foaming power. When this was used alone as a main component of a cleaning agent, there was generally a problem in foaming power.
[0004] このような起泡性の問題を改良するために、 硫酸エステル系界面活性剤お よびリン酸エステル系界面活性剤を含有する洗浄剤組成物が開示されている 力《 (例えば特許文献 1及び特許文献 2 ) 、 起泡力は満足できるものではなく 、 すすぎ性については言及されていない。 また、 リン酸エステル系界面活性 剤とグリセリルエーテルを含有する洗浄剤組成物が開示されているが (特許 文献 3 ) 、 起泡力は十分に満足できるものではなかった。  [0004] In order to improve such foaming problems, a detergent composition containing a sulfate ester surfactant and a phosphate ester surfactant has been disclosed. 1 and Patent Document 2), the foaming power is not satisfactory, and no mention is made of rinsing properties. Further, although a detergent composition containing a phosphate ester surfactant and glyceryl ether has been disclosed (Patent Document 3), the foaming power was not sufficiently satisfactory.
特許文献 1 :特開 2 0 0 3 _ 3 1 3 5 8 5号公報  Patent Document 1: Japanese Laid-Open Patent Publication No. 2 2003-3 1 3 5 8 5
特許文献 2:特開 2 0 0 6 _ 2 2 1 1 6号公報  Patent Document 2: Japanese Patent Laid-Open No. 2 0 0 6 _ 2 2 1 1 6
特許文献 3:特開 2 0 0 5 _ 2 0 6 8 0 4号公報  Patent Document 3: Japanese Patent Laid-Open No. 2 0 0 5 _ 2 0 6 8 0 4
発明の開示  Disclosure of the invention
[0005] 本発明は、 次の成分 (A ) 、 (B ) 及び (C ) (A) (31) —般式 (1 ) で表されるリン酸モノエステル系界面活性剤と (a 2) —般式 (2) で表されるリン酸ジエステル系界面活性剤 との混合物であって、 その含有比率が重量比で (ai) (a2) =90 1 0 〜50 50であるリン酸エステル系界面活性剤: [0005] The present invention provides the following components (A), (B) and (C): (A) ( 31 ) — A mixture of a phosphate monoester surfactant represented by general formula (1) and (a 2 ) — a phosphate diester surfactant represented by general formula (2) there, in its content ratio by weight (ai) (a 2) = 90 1 0 ~50 50 a is a phosphate ester surfactant:
[化 1] [Chemical 1]
Figure imgf000004_0001
Figure imgf000004_0001
(式中、 R1、 R2及び R3はそれぞれ炭素数 8〜 1 8の直鎖もしくは分岐鎖のァ ルキル基もしくはアルケニル基を示し、 X1、 X2、 Yはそれぞれ水素原子、 ァ ルカリ金属原子、 アルカリ土類金属原子、 アルカノールァミン又はアンモニ ゥ厶を示し、 平均付加モル数 k、 m及び nはそれぞれ 0~1 0の数を示す) (In the formula, R 1 , R 2 and R 3 each represent a linear or branched alkyl group or alkenyl group having 8 to 18 carbon atoms, and X 1 , X 2 and Y represent a hydrogen atom and an alkali, respectively. A metal atom, an alkaline earth metal atom, an alkanolamine, or an ammonium salt, and the average number of moles added, k, m, and n are each 0 to 10)
(B) —般式 (3) (B) — General formula (3)
R40 (C H2C H20) PS 03M R 4 0 (CH 2 CH 2 0) P S 0 3 M
(式中、 R4は炭素数 8〜 1 8のアルキル基もしくはアルケニル基を示し、 M はアルカリ金属原子、 アルカリ土類金属原子、 アルカノールァミン、 アンモ ニゥム又は塩基性ァミノ酸を示し、 平均付加モル数 pは 0〜 5の数を示す。 (In the formula, R 4 represents an alkyl group or alkenyl group having 8 to 18 carbon atoms, M represents an alkali metal atom, an alkaline earth metal atom, an alkanolamine, an ammonium or a basic amino acid, and an average addition. Mole number p shows the number of 0-5.
)  )
で表される硫酸エステル系界面活性剤; A sulfate ester surfactant represented by:
(C) (C- 1 ) 炭素数 6〜1 2の直鎖もしくは分岐鎖のアルキル基もし <はアルケニル基を有する 1種以上のグリセリルエーテル、 及び  (C) (C-1) a linear or branched alkyl group having 6 to 12 carbon atoms, wherein <is one or more glyceryl ethers having an alkenyl group, and
(C-2) —般式 (4)  (C-2) — General formula (4)
R50 (AO) qR6 (4) R 5 0 (AO) q R 6 (4)
(式中、 R5は炭素数 6〜 1 0の直鎖もしくは分岐鎖のアルキル基もしくはァ ルケ二ル基を示し、 R6は水素原子又はメチル基を示し、 A Oは炭素数 2〜 4 のアルキレンォキシ基を示し、 平均付加モル数 qは 0. 5~3の数を示す。(In the formula, R 5 represents a linear or branched alkyl group or alkyl group having 6 to 10 carbon atoms, R 6 represents a hydrogen atom or a methyl group, and AO represents 2 to 4 carbon atoms. The average number of added moles q is a number of 0.5 to 3.
) )
で表される化合物から選ばれる 1種以上;  One or more selected from the compounds represented by:
を含有する洗浄剤組成物を提供するものである。  The cleaning composition containing this is provided.
[0008] また、 本発明は、 該洗浄剤組成物を身体に適用する身体の洗浄方法を提供 するものである。 [0008] The present invention also provides a method for cleaning the body by applying the cleaning composition to the body.
更に、 本発明は、 該洗浄剤組成物の身体の洗浄への使用を提供するもので あ^ o  Furthermore, the present invention provides use of the cleaning composition for body cleaning.
発明の詳細な説明  Detailed Description of the Invention
[0009] 本発明は、 皮膚等に対する刺激が少なく、 起泡性に優れ、 泡質がクリーミ 一で、 かつすすぎ性が良好な洗浄剤組成物を提供することを目的とする。 本発明の洗浄剤組成物は、 皮膚等に対する刺激が少なく、 起泡性に優れ、 泡質がクリーミーで、 かつすすぎ性が良好である。  [0009] An object of the present invention is to provide a detergent composition that is less irritating to the skin and the like, is excellent in foaming properties, has a foam quality of creamy, and has good rinsing properties. The cleaning composition of the present invention is less irritating to the skin and the like, has excellent foaming properties, has a creamy quality, and has good rinsing properties.
[0010] 本発明に用いる低刺激性の基剤である成分 (A) の一般式 (1 ) 及び (2 ) で表されるリン酸エステルにおいて、 R1、 R2及び R3としては炭素数 1 0〜 1 6、 更に 1 2〜1 4のアルキル基であるのが好ましく、 X1、 X2及び Yは力 リウム又はナトリウムのようなアル力リ金属原子、 又はトリエタノールアミ が好ましく、 特に水に対する溶解性の点からカリウムが好ましい。 エチレン ォキシド平均付加モル数 k、 m及び nは、 起泡力の観点から、 0〜4モル、 さらに 0〜2、 より更に 0〜 1モルが好ましい。 [0010] In the phosphoric acid ester represented by the general formulas (1) and (2) of the component (A), which is a hypoallergenic base used in the present invention, R 1 , R 2 and R 3 are each a carbon number It is preferably an alkyl group of 10 to 16, more preferably 12 to 14 , and X 1 , X 2 and Y are preferably an alkali metal atom such as gallium or sodium, or triethanolami, particularly Potassium is preferable from the viewpoint of solubility in water. The average number of moles of ethylene oxide added k, m and n is preferably 0 to 4 moles, more preferably 0 to 2 and even more preferably 0 to 1 mole from the viewpoint of foaming power.
[0011] 成分 (A) 中のアルキルリン酸モノエステル (ai) とアルキルリン酸ジェ ステル (a 2) との含有比率は、 配合の容易さの観点から、 重量比 (a i) ( a2) =90 1 0〜50 50であり、 85 1 5〜 60 40が好ましく 、 80 20〜70 30が更に好ましい。 [0011] The content ratio of the alkyl phosphate monoester ( ai ) and the alkyl phosphate ester (a 2 ) in the component (A) is determined by weight ratio ( ai ) (a 2 ) from the viewpoint of ease of blending. = 90 10 to 50 50, 85 15 to 60 40 is preferable, and 80 20 to 70 30 is more preferable.
重量比 (a / (a2) が 50 50未満では起泡性が劣り、 重量比 (a / (a2) が 90 1 0超ではアルキルリン酸エステル混合物の融点が高くな り配合が困難となる。 When the weight ratio (a / (a 2 ) is less than 50 50, the foaming property is poor, and when the weight ratio (a / (a 2 ) is more than 90 10, the melting point of the alkyl phosphate ester mixture becomes high, which makes mixing difficult. Become.
[0012] 成分 (A) のリン酸エステル系界面活性剤の含有量は、 泡立ち、 洗浄力及 び配合の容易さの観点から、 本発明の洗浄剤組成物の 1 ~ 1 5重量%が好ま しく、 2~ 1 0重量%が更に好ましく、 3~ 1 0重量%がより更に好ましい [0012] The content of the phosphoric acid ester-based surfactant of component (A) is foaming, detergency and And 1 to 15% by weight of the cleaning composition of the present invention is preferable, 2 to 10% by weight is more preferable, and 3 to 10% by weight is still more preferable.
[0013] 成分 (A) は、 例えば対応する脂肪族アルコール又は対応する脂肪族アル コールにエチレンォキシドを付加し、 平均付加モル数 0超〜 1 0となったェ トキシレートと、 無水リン酸、 オルトリン酸、 ポリリン酸またはォキシ塩化 リン酸等のリン酸化剤とを反応させ得られるリン酸エステル、 又はそのリン 酸エステルを水酸化ナトリゥム、 水酸化力リゥム等のアル力リで一部又は完 全に中和することにより得られるリン酸エステル塩である。 (a J / (a 2 ) は、 脂肪族アルコールとリン酸化剤に含まれる水との比率でコントロール することができる。 [0013] Component (A) is, for example, an ethylene oxide added to a corresponding aliphatic alcohol or a corresponding aliphatic alcohol to obtain an ethoxylate having an average addition mole number of more than 0 to 10; phosphoric anhydride; Phosphoric acid ester obtained by reacting phosphoric acid such as orthophosphoric acid, polyphosphoric acid or oxyphosphoric acid, or the phosphoric acid ester partially or completely with sodium hydroxide, hydroxylated lithium, etc. It is a phosphoric ester salt obtained by neutralization. (A J / (a 2 ) can be controlled by the ratio between the aliphatic alcohol and the water contained in the phosphorylating agent.
(a ,) / (a 2) =90 1 0〜 50 50を得る方法としては、 例えば 反応時に無水リン酸と水を含むオルトリン酸を用いて、 原料アルコールと水 の比率を調整し直接的に (a J / (a 2) の比率をコントロールする方法や 、 (a J (a 2) = 1 00 0~95 5のリン酸エステルと、 (a J Z (a 2) =50 50のリン酸エステルを適当な割合で混合する方法等がある As a method of obtaining (a,) / (a 2 ) = 90 10 0-50 50, for example, by using orthophosphoric acid containing phosphoric anhydride and water during the reaction, the ratio of the raw alcohol and water is directly adjusted. (A method of controlling the ratio of a J / (a 2 ), (a J (a 2 ) = 100-95 5 phosphate ester, (a JZ (a 2 ) = 50 50 phosphate ester There is a method of mixing
[0014] 成分 (B) の一般式 (3) で表される硫酸エステル系界面活性剤において 、 R4は起泡性の観点から、 平均炭素数 8〜 1 8、 好ましくは 1 0〜 1 6、 更 に好ましくは 1 0 ~ 1 4の直鎖もしくは分岐鎖のアルキル基もしくはァルケ ニル基である。 In the sulfate ester surfactant represented by the general formula (3) of component (B), R 4 has an average carbon number of 8 to 18, preferably 10 to 16 from the viewpoint of foamability. More preferably, they are 10 to 14 linear or branched alkyl groups or alkenyl groups.
また、 Mはカリウムやナトリウムなどのアルカリ金属、 トリエタノールァ ミン、 又はアンモニゥムが好ましく、 更に水に対する溶解性、 起泡性の観点 からカリウム、 ナトリウム、 又はアンモニゥムが好ましい。  M is preferably an alkali metal such as potassium or sodium, triethanolamine, or ammonium, and more preferably potassium, sodium, or ammonium from the viewpoint of solubility in water and foaming.
[0015] 成分 (B) の含有量は、 本発明の洗浄剤組成物の洗浄性、 起泡性の観点か ら、 5〜40重量%が好ましく、 5〜35重量%が更に好ましく、 5〜20 重量%がより更に好ましい。 [0015] The content of the component (B) is preferably 5 to 40% by weight, more preferably 5 to 35% by weight, from the viewpoint of detergency and foaming property of the cleaning composition of the present invention, 20% by weight is even more preferred.
本発明の洗浄剤組成物において、 成分 (A) と成分 (B) の好ましい含有 量は上記のとおりであるが、 更に成分 (A) と成分 (B) の含有比率は重量 比で成分 (B) 成分 (A) =0. 5~20、 更に"!〜 1 0とすることが洗 浄カ、 起泡力、 泡質及びすすぎ性の点から好ましく、 より更に 2~5が好ま しい。 In the cleaning composition of the present invention, the preferred content of component (A) and component (B) Although the amount is as described above, the content ratio of the component (A) and the component (B) is the weight ratio of the component (B), the component (A) = 0.5 to 20, and “! To 10”. Is preferred from the viewpoints of washing power, foaming power, foam quality and rinsing properties, and 2 to 5 are more preferred.
[0016] 成分 (C— 1 ) のグリセリルエーテルは、 炭素数 6〜1 2の直鎖もしくは 分岐鎖のアルキル基もしくはアルケニル基を有するもので、 例えば n—へキ シル基、 イソへキシル基、 n—ヘプチル基、 n—ォクチル基、 2 _ェチルへ キシル基、 n_ノニル基、 n_デシル基、 n_ラウリル基等の炭素数 6〜1 2のアルキル基を有するものが好ましく、 更に炭素数 6〜1 1、 より更に炭 素数 6〜1 0、 とりわけ炭素数 8のアルキル基を 1又は 2個、 更に 1個有す るのが好ましい。  [0016] The glyceryl ether of the component (C-1) has a linear or branched alkyl group or alkenyl group having 6 to 12 carbon atoms, such as an n-hexyl group, an isohexyl group, Those having an alkyl group having 6 to 12 carbon atoms such as n-heptyl group, n-octyl group, 2_ethylhexyl group, n_nonyl group, n_decyl group, n_lauryl group, and the like are preferable. It is preferable to have 1 or 2 alkyl groups having 6 to 11 carbon atoms, 6 to 10 carbon atoms, especially 8 carbon atoms, and more preferably one.
成分 (C— 1 ) のグリセリルエーテルは、 1種以上を用いることができ、 全組成中に 0. 1 ~20重量%、 更に 0. 1 ~ 1 0重量%、 より更に 0. 1 ~ 5重量%配合するのが、 すすぎ性および起泡力の点で好ましい。  One or more glyceryl ethers of component (C-1) can be used, and 0.1 to 20% by weight, further 0.1 to 10% by weight, and further 0.1 to 5% by weight in the total composition. % Is preferable in terms of rinsing properties and foaming power.
成分 (C_ 1 ) は、 例えば対応するグリシジルエーテルと水を 1 00~2 30 °Cで加水分解して得ることができる。  The component (C_1) can be obtained, for example, by hydrolyzing the corresponding glycidyl ether and water at 100 to 230 ° C.
[0017] 成分 (C_2) の前記一般式 (3) で表されるアルコールのアルキレンォ キシド付加物において、 R5は炭素数 6〜 1 0、 好ましくは炭素数 8〜 1 0の 直鎖もしくは分岐鎖のアルキル基もしくはアルケニル基であり、 更に炭素数 8のアルキル基が好ましい。 AOは炭素数 2 ~ 4のアルキレンォキシ基であ り、 更に炭素数 2~3のアルキレンォキシ基が好ましく、 より更に炭素数 3 のアルキレンォキシ基が好ましい。 具体的には、 エチレンォキシ基、 プロピ レンォキシ基及びブチレンォキシ基等が挙げられ、 エチレンォキシ基及びプ ロピレンォキシ基が好ましく、 更にプロピレンォキシ基が好ましい。 平均付 加モル数 qは 0. 5〜 3の数を示すが、 1〜3が好ましく、 更に 2〜3が好 ましい。 成分 (C_2) における AOの付加モル数の最も多い成分を AOmaxと した時、 精製等の製造コス卜の負荷を低減させるような経済性の観点から A Omaxが成分 ( C _ 2 ) 全体の 70重量%以下であるのが好ましく、 60重量% 以下であるのが更に好ましく、 より更に 50重量%以下であるのが好ましい 。 更に AOが炭素数 2のォキシアルキレン基、 即ちォキシエチレン基である 場合、 AOmaxが成分 (C_ 2) 全体の 60重量%以下、 更に 50重量%以下、 より更に 40重量%以下であるのが好ましい。 また、 更に AOが炭素数 3の ォキシアルキレン基、 即ちォキシプロピレン基である場合、 AOmaxが成分 (C - 2) 全体の 7 0重量%以下、 更に 60重量%以下、 より更に 50重量%以 下であるのが好ましい。 R6は水素原子又はメチル基を示し、 更に好ましくは 水素原子である。 成分 (C_ 2) は、 1種以上を用いることができ、 全組成 中に 0. 1〜20重量%、 更に0. 1〜 1 5重量0 /o、 より更に 0. 1〜 1 0 重量%配合するのが、 すすぎ性および起泡力の点で好ましい。 [0017] In the alkylene oxide adduct of the alcohol represented by the general formula (3) of the component (C_2), R 5 is a linear or branched chain having 6 to 10 carbon atoms, preferably 8 to 10 carbon atoms. And an alkyl group having 8 carbon atoms is preferred. AO is an alkyleneoxy group having 2 to 4 carbon atoms, more preferably an alkyleneoxy group having 2 to 3 carbon atoms, and still more preferably an alkyleneoxy group having 3 carbon atoms. Specific examples include an ethyleneoxy group, a propyleneoxy group, and a butyleneoxy group. An ethyleneoxy group and a propyleneoxy group are preferable, and a propyleneoxy group is more preferable. The average added mole number q represents a number of 0.5 to 3, preferably 1 to 3, and more preferably 2 to 3. When the component with the largest number of moles of AO added in component (C_2) is AO max , AO max is the total component (C _ 2) from the viewpoint of economy that reduces the burden of manufacturing costs such as refining. 70% by weight or less is preferable, 60% by weight More preferably, it is more preferably 50% by weight or less. Further, when AO is an oxyalkylene group having 2 carbon atoms, that is, an oxyethylene group, AO max is 60% by weight or less, further 50% by weight or less, and further 40% by weight or less of the total component (C_2). preferable. Further, when AO is an oxyalkylene group having 3 carbon atoms, that is, an oxypropylene group, AO max is 70% by weight or less, further 60% by weight or less, and further 50% by weight of the total component (C-2). % Or less is preferable. R 6 represents a hydrogen atom or a methyl group, more preferably a hydrogen atom. One or more components (C_ 2) can be used, and the total composition is 0.1 to 20% by weight, further 0.1 to 15% by weight 0 / o, and further 0.1 to 10% by weight. It is preferable to blend them in terms of rinsing properties and foaming power.
成分 (C_ 2) は、 例えば対応する脂肪族アルコールにプロピレンォキシ ド及び 又はエチレンォキシドを反応させた後、 該原料アルコールを蒸留留 去して得ることができる。  The component (C_2) can be obtained, for example, by reacting propylene oxide and / or ethylene oxide with the corresponding aliphatic alcohol and then distilling the raw material alcohol.
成分 (C) 全体の配合量は、 本発明の洗浄剤組成物に 0. 1 ~ 20重量% が好ましく、 0. 1 ~ 1 5重量%が更に好ましく、 0. 1 ~ 1 0重量%がよ り更に好ましい。  The total amount of component (C) is preferably 0.1 to 20% by weight, more preferably 0.1 to 15% by weight, more preferably 0.1 to 10% by weight in the cleaning composition of the present invention. Even more preferable.
[0018] 本発明洗浄剤組成物は、 洗顔剤、 シャンプー、 ボディシャンプー等の皮膚 洗浄剤又は毛髪洗浄剤のような身体用洗浄剤として有用な洗浄剤組成物であ るが、 更に、 洗顔剤、 ボディシャンプー等の皮膚洗浄剤として使用するのが 好ましい。 これらの洗浄剤組成物には、 その目的に応じ任意成分を配合する ことができる。 ここで、 任意成分としては、 通常これらの洗浄剤に配合され る他のァニオン性界面活性剤、 非イオン性界面活性剤、 両性界面活性剤、 力 チオン性界面活性剤、 コンディショニング成分などが挙げられる。  [0018] The cleaning composition of the present invention is a cleaning composition useful as a skin cleaning agent such as a facial cleanser, a shampoo, a body shampoo, or a body cleaner such as a hair cleaner. It is preferably used as a skin cleanser such as body shampoo. These cleaning compositions can contain optional components depending on the purpose. Here, examples of optional components include other anionic surfactants, nonionic surfactants, amphoteric surfactants, force thionic surfactants, and conditioning components that are usually blended in these detergents. .
[0019] 他のァニオン界面活性剤としては、 脂肪酸塩、 スルホコハク酸系界面活性 剤、 スルホサクシナメート系界面活性剤、 ポリオキシアルキレンアルキルァ ミ ドエーテル硫酸塩、 モノグリセライ ド硫酸塩、 ォレフインスルホン酸塩、 アルカンスルホン酸塩、 ァシル化イセチオン酸塩、 ァシル化アミノ酸塩、 成 分 (A) 以外のポリオキシアルキレンアルキルエーテルリン酸塩等が挙げら れ;非イオン界面活性剤としては、 アルキルポリダルコシド、 ショ糖脂肪酸 エステル、 ポリグリセリン脂肪酸エステル、 脂肪酸アル力ノールアミ ド、 ァ ルキルアミンォキサイ ド、 脂肪酸多価アルコールエステル等が挙げられる。 またカチオン界面活性剤としては、 直鎖又は分岐鎖のモノ又はジ長鎖アルキ ル第 4級ァンモニゥム塩、 モノ又はジ長鎖アルキル第 3級ァミン等が挙げら れ;両性界面活性剤としては、 アミ ドアミノ酸系活性剤、 カルボべタイン系 活性剤、 スルホベタイン系活性剤、 アミ ドスルホベタイン系活性剤、 イミダ ゾリニゥムベタイン系活性剤、 アミノ酸系べタイン活性剤、 ホスホべタイン 系活性剤等が挙げられる。 [0019] Other anionic surfactants include fatty acid salts, sulfosuccinic acid surfactants, sulfosuccinamate surfactants, polyoxyalkylene alkylamide ether sulfates, monoglyceride sulfates, and olefin sulfones. Acid salts, alkane sulfonates, acylated isethionates, acylated amino acid salts, polyoxyalkylene alkyl ether phosphates other than the component (A), etc. Examples of the nonionic surfactant include alkylpolydarcoside, sucrose fatty acid ester, polyglycerin fatty acid ester, fatty acid alcohol amide, alkylamine oxide, and fatty acid polyhydric alcohol ester. Examples of cationic surfactants include linear or branched mono- or di-long chain alkyl quaternary ammonium salts, mono- or di-long chain alkyl tertiary amines, and the like. Amide amino acid-based activator, Carbobetaine-based activator, Sulfobetaine-based activator, Amidosulfobetaine-based activator, Imidazolinium betaine-based activator, Amino acid-based betaine-activator, Phosphobetaine-based activator Etc.
[0020] コンディショニング成分としては、 高級アルコール、 シリコーン及びシリ コーン誘導体、 ラノ リン、 スクワレン、 炭化水素、 蛋白誘導体、 ポリエチレ ングリコールの脂肪酸エステル等の油剤、 カチオン化セルロース、 カチオン 化グァガムやマーコート 5 5 0 (ナルコ社製) 、 ソフ トケア K G— 3 0 1 W [花王 (株) 製] 等のカチオンポリマー等が挙げられる。  [0020] Examples of conditioning components include higher alcohols, silicone and silicone derivatives, lanolin, squalene, hydrocarbons, protein derivatives, polyethylene glycol fatty acid esters and other oil agents, cationized cellulose, cationized guagam and marcoat. (Naruco Co., Ltd.), Softcare KG-3301 W [manufactured by Kao Corporation], and the like.
[0021 ] また、 洗浄剤組成物中に通常使用されるその他の成分、 例えば、 メチルセ ルロース、 ヒドロキシェチルセルロース、 カルボキシビ二ルポリマー、 キサ ンタンガム等の多糖類等の水溶性高分子;ポリオキシアルキレンソルビタン エステル、 ポリオキシエチレングリコールジステアレート、 エタノール等の 粘度調整剤; エチレンジァミン四酢酸 (E D T A ) 、 ホスホン酸塩類等のキ レート剤; メチルパラベン、 ブチルパラベン等の防腐剤; ビタミンやその前 駆体等の有効成分; レシチン、 ゼラチン等の動植物抽出物又はその誘導体; ナイ口ンゃポリエチレン等のポリマー微粉体; グリチルリチン酸ジ力リウム 等の消炎剤; トリクロサン、 トリクロロカルバン、 ォクトビロックス、 ジン クピリチオン等の殺菌剤や抗フケ剤; ジブチルヒドロキシトルエン等の酸化 防止剤;パール化剤、 紫外線吸収剤、 p H調整剤、 色素、 香料、 水を本発明 の効果を損なわない範囲で必要に応じて配合することができる。  [0021] In addition, other components usually used in the detergent composition, for example, water-soluble polymers such as polysaccharides such as methylcellulose, hydroxyethylcellulose, carboxyvinyl polymer, xanthan gum; polyoxyalkylene Viscosity modifiers such as sorbitan ester, polyoxyethylene glycol distearate, ethanol, etc .; Ethylenediamine tetraacetic acid (EDTA), phosphonates and other chelating agents; methylparaben, butylparaben and other preservatives; vitamins and precursors thereof Active ingredients of: Lecithin, animal and plant extracts such as gelatin or derivatives thereof; polymer fine powder such as Nai Nya polyethylene; anti-inflammatory agent such as dipotassium glycyrrhizinate; And anti-dandruff agents; Antioxidants such as dibutylhydroxytoluene; pearlizing agents, ultraviolet absorbers, pH adjusting agents, dyes, fragrances, and water can be blended as necessary within a range not impairing the effects of the present invention.
本発明の洗浄剤組成物は、 p H 4〜 8であるものが好ましい。 本発明の洗浄剤組成物は、 硬度が 1〜3 0 ° D Hの水と共に用いられるの が好ましい。 The detergent composition of the present invention preferably has a pH of 4-8. The cleaning composition of the present invention is used with water having a hardness of 1 to 30 ° DH. Is preferred.
また、 ここで使用する水は p Hが 4 ~ 9のものが好ましい。  The water used here preferably has a pH of 4 to 9.
[0022] 本発明の洗浄剤組成物は、 常法に従って製造できる。 本発明の洗浄剤組成 物の剤型について特に制限はなく、 従来より公知の種々の剤型、 例えば液体 ボディシャンプー、 クリーム状洗顔料等とすることができる。 本発明の洗浄 剤組成物は特に皮膚、 毛髪等の身体用洗浄剤として好適である。 [0022] The cleaning composition of the present invention can be produced according to a conventional method. There are no particular limitations on the dosage form of the cleaning composition of the present invention, and various conventionally known dosage forms such as liquid body shampoos, cream facial cleansings, and the like can be used. The cleaning composition of the present invention is particularly suitable as a cleaning agent for body such as skin and hair.
[0023] 製造例 1 [0023] Production Example 1
50 OmLの反応容器に窒素雰囲気下で原料アルコール (ラウリルアルコ ール) 1 87. 3 g ( 1. 0モル) を加え、 85重量0 /0のオルトリン酸 3 1 ■ 9 g 〔Ρ205 · n H20として表すと Ρ205 1 9. 6 g (0. 1 4モル) H20 1 2. 3 g (0. 68モル) 〕 を加え 35 °Cにて攪拌■混合した。 更 に五酸化リン (有効分 98. 5重量%) 62. 1 g (0. 43モル) を攪拌 しながら 60分間で徐々に添加した。 温度は 65°Cまで上昇し、 更に昇温し 80°Cで 1 2時間反応を行った。 更に水を 1 0. 0 g加え 80°Cで 3時間加 水分解を行って得られたリン酸エステルを水酸化力リウムで中和して表 1に 示すラウリルホスフェート K塩 (モノラウリル体 ジラウリル体 =80 2 0) を得た。 50 starting alcohol (lauryl alcohol) under a nitrogen atmosphere in a reaction vessel OmL 1 87. 3 g (1. 0 mol) was added, 85 weight 0/0 of orthophosphoric acid 3 1 ■ 9 g [[rho 2 0 5 · When expressed as n H 2 0 Ρ 2 0 5 1 9.6 g (0.14 mol) H 2 0 1 2.3 g (0.68 mol)] was added and stirred at 35 ° C and mixed . Further, 62.1 g (0.43 mol) of phosphorus pentoxide (effective content: 98.5% by weight) was gradually added over 60 minutes with stirring. The temperature rose to 65 ° C, the temperature was further raised, and the reaction was carried out at 80 ° C for 12 hours. Further, 10 g of water was added, and the phosphoric acid ester obtained by hydrolyzing at 80 ° C for 3 hours was neutralized with potassium hydroxide and lauryl phosphate K salt (monolauryl dilauryl) shown in Table 1. Body = 80 2 0).
[0024] 製造例 2 [0024] Production Example 2
製造例 1 と同様にして、 モノラウリル体 ジラウリル体 =60 40にな るように、 ラウリルアルコールに対する水の量を調節し、 反応させ、 表 1に 示すラウリルホスフェート K塩 (モノラウリル体 ジラウリル体 = 60 4 0) を得た。  In the same manner as in Production Example 1, the amount of water with respect to lauryl alcohol was adjusted and reacted so that the monolauryl dilauryl body = 60 40, and the lauryl phosphate K salt (monolauryl dilauryl body = 60 4 0) was obtained.
[0025] 製造例 3 [0025] Production Example 3
製造例 1 と同様にして、 モノラウリル体 ジラウリル体 =70 30にな るように、 ラウリルアルコールに対する水の量を調節し、 反応させ、 得られ たリン酸エステルをトリエタノールァミンで中和し、 表 1に示すラウリルホ スフヱートトリエタノールアミン塩 (モノラウリル体 ジラウリル体 = 70 30) を得た。 In the same manner as in Production Example 1, the amount of water relative to lauryl alcohol was adjusted and reacted so that the monolauryl dilauryl body = 70 30, and the resulting phosphate ester was neutralized with triethanolamine. The lauryl phosphate triethanolamine salt shown in Table 1 (monolauryl dilauryl = 70 30)
[0026] 製造例 4 [0026] Production Example 4
50 OmLの反応容器に窒素雰囲気下で原料アルコール (ラウリルアルコ ール、 巳0 =平均1モル付加品) 230. 4 g (1. 0モル) を加え、 85 重量%のオルトリン酸 31. 9 g 〔P205■ n H20として表すと P 205 1 9. 6 g (0. 1 4モル) H20 1 2. 3 g (0. 68モル) 〕 を加え 35 °Cにて攪拌 '混合した。 更に五酸化リン (有効分 98. 5重量%) 62. 1 g (0. 43モル) を攪拌しながら 60分間で徐々に添加した。 温度は 65 °Cまで上昇し、 更に昇温し 80°Cで 1 2時間反応を行った。 更に水を 1 0. 0 g加え 80°Cで 3時間加水分解を行って得られたリン酸エステルを水酸化 カリウムで中和して表 1に示すポリオキシエチレン (1 ) ラウリルエーテル ホスフェート K塩 (モノラウリル体 ジラウリル体 =80 20) を得た。 Raw material alcohol (lauryl alcohol, 巳 0 = average 1 mol addition product) was added to a 50 OmL reaction vessel under a nitrogen atmosphere, and 23.4 g (1.0 mol) was added, and 39.9 g of 85 wt% orthophosphoric acid was added. Add [P 2 0 5 ■ n H 2 0 and P 2 0 5 1 9.6 g (0.14 mol) H 2 0 1 2.3 g (0.68 mol)] to 35 ° C Stir and mix. Further, 62.1 g (0.43 mol) of phosphorus pentoxide (effective content 98.5% by weight) was gradually added over 60 minutes with stirring. The temperature rose to 65 ° C, the temperature was further raised, and the reaction was carried out at 80 ° C for 12 hours. Further, 10 g of water was added, and the phosphate ester obtained by hydrolysis at 80 ° C for 3 hours was neutralized with potassium hydroxide, and the polyoxyethylene (1) lauryl ether phosphate K salt shown in Table 1 was obtained. (Monolauryl body dilauryl body = 80 20) was obtained.
[0027] 製造例 5 [0027] Production Example 5
製造例 1 と同様にして、 ラウリルアルコール、 EO =平均 1モル付加品を ミリスチルアルコール、 EO =平均 1モル付加品に変え、 モノミリスチル体 ジミリスチル体 = 85 1 5になるように、 ミリスチルアルコール、 EO =平均 1モル付加品に対する水の量を調節し、 反応させ、 表 1に示すポリオ キシエチレン (1 ) ミリスチルエーテルホスフェート K塩 (モノミリスチル 体 ジミリスチル体 =85 1 5) を得た。  In the same manner as in Production Example 1, change lauryl alcohol, EO = average 1 mol addition product to myristyl alcohol, EO = average 1 mol addition product, so that monomyristyl dimyristyl = 85 1 5 = Adjusting the amount of water relative to an average 1 mol addition product, reaction was carried out to obtain polyoxyethylene (1) myristyl ether phosphate K salt (monomyristyl dimyristyl = 85 15) shown in Table 1.
[0028] 製造例 6 [0028] Production Example 6
製造例 1 と同様にして、 ラウリルアルコール、 EO =平均 1モル付加品を ラウリルアルコール、 EO =平均 2モル付加品に変え、 モノラウリル体 ジ ラウリル体 = 75 25になるように、 ラウリルアルコール、 EO =平均 2 モル付加品に対する水の量を調節し、 反応させ、 表 1に示すポリオキシェチ レン (2) ラウリルエーテルホスフェート K塩 (モノラウリル体 ジラウリ ル体 = 75/25) を得た。  In the same manner as in Production Example 1, lauryl alcohol, EO = average 1 mol addition product was changed to lauryl alcohol, EO = average 2 mol addition product, so that monolauryl dilauryl product = 75 25, lauryl alcohol, EO = The amount of water relative to the average 2 mol addition product was adjusted and reacted to obtain polyoxyethylene (2) lauryl ether phosphate K salt (monolauryl dilauryl = 75/25) shown in Table 1.
[0029] 製造例 7 [0029] Production Example 7
2—ェチルへキシルグリシジルエーテル 208 g、 水 1 04. 8 g、 ラウ リン酸 5. 82 g及び水酸化カリウム 1 8. 5 gをオートクレープに入れ、 1 40°Cで 5時間攪拌した。 減圧下 (6. 67 k P a) 、 1 00°Cで脱水後 、 ラウリン酸 9. 7 g及び水酸化カリウム 2. 72 gを加え、 1 60°Cで 1 5時間反応し、 その後減圧蒸留 (53〜67 P a、 1 20〜 1 23°C) によ り精製して表 1に示す 2—ェチルへキシルグリセリルエーテルを得た。 2-Ethylhexyl glycidyl ether 208 g, water 104.8 g, laur 5.82 g of phosphoric acid and 18.5 g of potassium hydroxide were placed in an autoclave and stirred at 140 ° C. for 5 hours. After dehydration at 100 ° C under reduced pressure (6.67 k Pa), add 9.7 g of lauric acid and 2.72 g of potassium hydroxide, react at 160 ° C for 15 hours, and then distilled under reduced pressure (53-67 Pa, 120-123 ° C.), 2-ethylhexyl glyceryl ether shown in Table 1 was obtained.
[0030] 製造例 8 [0030] Production Example 8
製造例 7と同様にして、 2—ェチルへキシルグリシジルエーテルを n—ォ クチルグリシジルエーテルに変えて、 表 1に示す n—ォクチルグリセリルェ 一テルを得た。  In the same manner as in Production Example 7, 2-ethylhexyl glycidyl ether was changed to n-octyl glycidyl ether to obtain n-octyl glyceryl ethers shown in Table 1.
[0031] 製造例 9 [0031] Production Example 9
1—ォクタノール (カルコール 0898、 花王 (株) 製) 1 61 5. 0 g (1 2. 35mo I ) と水酸化力リゥム 6. 9 g (0. 1 2 m o I ) をォー トクレープに仕込み、 1 1 0°C、 1 3. 3 k P aで脱水後、 1 20°Cでプロ ピレンォキシド 1 434 g (24. 69 0 1 ) を0. 3MP aで圧入しな がら付加反応を行った。  1-octanol (Calcoal 0898, manufactured by Kao Corporation) 1 61 5. 0 g (1 2. 35 mo I) and hydroxylated power of 6.9 g (0.12 mo I) were charged into the autoclave, After dehydration at 1 10 ° C and 13.3 kPa, addition reaction was carried out at 120 ° C while injecting 1434 g (24. 69 0 1) of propylene oxide at 0.3 MPa.
反応終了後、 同一反応温度で 6時間熟成を行った後、 80°Cまで冷却した 後処理として、 得られた反応組成物に合成吸着剤 (キヨ一ワード 600 S、 協和化学工業 (株) ) 55 gを加えて、 4. 0 k P aにて 1時間処理した 後、 ろ過により触媒を除去した。  After completion of the reaction, after aging at the same reaction temperature for 6 hours, after cooling to 80 ° C, the resulting reaction composition was combined with a synthetic adsorbent (Kyoichi Ward 600 S, Kyowa Chemical Industry Co., Ltd.) After adding 55 g and treating with 4.0 k Pa for 1 hour, the catalyst was removed by filtration.
次いで得られたろ液 1 000 gについて、 1 30°C、 1. 3 k P aの条件 で 1—ォクタノールを蒸留により留去した。 更に 1 45°C、 6. O k P a、 5時間の条件で水蒸気 1 00 gを吹き込む水蒸気処理を行い、 表 1に示すジ プロピレングリコールモノォクチルエーテルを得た。  Subsequently, 1-octanol was distilled off from 1 000 g of the obtained filtrate under the conditions of 130 ° C. and 1.3 kPa. Further, steam treatment was performed by blowing 100 g of steam under the conditions of 145 ° C., 6. O k Pa, and 5 hours to obtain dipropylene glycol monooctyl ether shown in Table 1.
[0032] 製造例 1 0 [0032] Production Example 1 0
製造例 9と同様にして、 1—ォクタノールを 2 _ェチルへキシルアルコー ルに、 プロピレンォキシドをエチレンォキシドに変えて、 表 1に示すジェチ レングリコール 2 _ェチルへキシルエーテルを得た。 [0033] 実施例 1 ~ 20及び比較例 1 ~ 6 In the same manner as in Production Example 9, 1-octanol was changed to 2_ethylhexyl alcohol, and propylene oxide was changed to ethylene oxide to obtain the ethylene glycol 2_ethylhexyl ether shown in Table 1. [0033] Examples 1 to 20 and Comparative Examples 1 to 6
表 1に示す組成の洗浄組成物を、 常法に従って各成分を 70°Cで混合して 製造 ( 1"1を6~7に調整) し、 これを手のひらに 1 g塗布して手、 腕を洗 浄したときの起泡性、 泡質およびすすぎ性を専門パネラー 1 0名により下記 の評価基準に従い評価した。 結果を表 1に示す。  A cleaning composition having the composition shown in Table 1 was prepared by mixing each component at 70 ° C according to a conventional method (1 "1 was adjusted to 6-7), and 1 g of this was applied to the palm of the hand and arm. Foaming properties, foam quality and rinsing properties when washed were evaluated by 10 expert panelists according to the following evaluation criteria: Table 1 shows the results.
(起泡性)  (Foamability)
4 :泡量が非常に多い  4: The amount of foam is very large
3 :泡量が多い  3: Large amount of foam
2 :泡量がやや少ない  2: Slightly less foam
1 :泡量が少ない  1: Less foam
(泡質)  (Foam quality)
4 : きめ細かく、 かつ非常にクリーミーで良好な泡質  4: Fine, very creamy and good foam quality
3 : クリーミーで良好な泡質  3: Creamy and good foam quality
2 :ややクリーミーな泡質  2: Slightly creamy foam quality
1 :軽く粗い泡質  1: Light and rough foam
(すすぎ性)  (Rinse)
4 :ぬるつきがなく、 すすぎ性良好  4: No slickness, good rinsing
3 : ほぼぬるつきがなく、 すすぎ性やや良好  3: Almost no slickness, slightly good rinsing
2 :ややぬるつき、 すすぎ性やや悪い  2 : Slightly sticky, slightly rinsable
1 :ぬるつき、 すすぎ性悪い  1 : Slimy, poor rinsing
ランク  Rank
A :平均評点が 3. 5以上  A: Average score of 3.5 or higher
B :平均評点が 2. 5以上、 3. 5未満  B: Average score is 2.5 or more and less than 3.5
C :平均評点が 1. 5以上、 2. 5未満  C: Average score is 1.5 or more and less than 2.5
D :平均評点が 1. 5未満  D: Average score is less than 1.5
[0034] [0034]
[ ] []
S.C000/.00Zdf/X3d ZY 98S9TI/.00Z OAV S.C000 / .00Zdf / X3d ZY 98S9TI / .00Z OAV
Figure imgf000015_0001
Figure imgf000015_0001
、一  One
,一  , One
 One
— 、 ,1Sfi 、 2mDl 、 .0Sfi%. —,, 1Sfi, 2mDl, .0Sfi%.
[0035] 実施例 21 -24 [0035] Examples 21 -24
下記の処方で、 p H 5. 0-7. 0の洗顔料、 全身洗浄料を製造した。 p Hはクェン酸、 水酸化カリウムによって調整した。 いずれも、 低刺激であり 、 使用する水の p Hが 4〜 5未満、 5〜8未満、 及び 8〜 9の全ての領域に おいても、 また、 使用する水の硬度が 1〜30° DHの全ての領域において も、 起泡性が良好で、 泡質がクリーミーであり、 すすぎ性が良好だった。  A face wash and whole body cleanser with a pH of 5.0-0.7.0 were prepared with the following formulation. pH was adjusted with citrate and potassium hydroxide. Both are hypoallergenic and the pH of the water used is less than 4-5, less than 5-8, and 8-9, and the hardness of the water used is 1-30 ° In all areas of DH, foaming was good, foam quality was creamy, and rinsing was good.
[0036] 実施例 21 (洗顔料)  Example 21 (face wash)
(成 分) (重量0 /o) ラウリルホスフエ一ト K塩 (Ingredient) (Weight 0 / o) Lauryl phosphate K salt
(モノラウリル体 ジラウリル体 = 75 25) 0. 5 ポリオキシエチレン (1 ) ラウリルエーテルホスフェート K塩 a)  (Monolauryl dilauryl = 75 25) 0.5 Polyoxyethylene (1) Lauryl ether phosphate K salt a)
(モノラウリル体 ジラウリル体 = 75 25) 1. 5 ポリオキシエチレン (2) ラウリル硫酸 N a b) 24. 0 ジプロピレングリコール 0. 5 ジプロピレングリコールモノォクチルエーテル 0. 4 ラウロイルヒドロキシスルホべタイン 1. 2 N, N—ジメチルアミノエチルメタクリル酸ジェチル硫酸塩■ N, N- ジメチルァクリルアミ ド■ジメタクリル酸ポリエチレングリコール共 重合体 4重量%水溶液 c) 2. 5 アクリル酸メタクリル酸アルキル共重合体 d) 0. 5 塩化ナトリウム 1. 0 硫酸ナトリウム 3. 0 ジステアリン酸エチレングリコール 2. 0 メチルパラベン 0. 2 プロピルパラベン 0. 1 (Monolauryl dilauryl = 75 25) 1.5 Polyoxyethylene (2) Lauryl sulfate N ab) 24.0 Dipropylene glycol 0.5 Dipropylene glycol monooctyl ether 0.4 Lauroyl hydroxysulfobetaine 1. 2 N, N-dimethylaminoethyl jetyl sulfate methacrylate ■ N, N-dimethylacrylamide ■ Polyethylene glycol dimethacrylate copolymer 4% by weight aqueous solution c) 2.5 Alkyl methacrylate copolymer d 0.5 sodium chloride 1.0 sodium sulfate 3.0 ethylene glycol distearate 2.0 methyl paraben 0.2 propyl paraben 0.1
B H T 0. 2 香料 0. 05 賴 バランス 計 1 00. 00 a) ( ) 内はエチレンォキシド平均付加モル数を示し、 一般式 (1 ) 及び (2) の k=m= n = 1である化合物。 BHT 0. 2 Fragrance 0. 05 賴 Balance Total 1 00. 00 a) In (), the average number of added moles of ethylene oxide is shown, and in the general formulas (1) and (2), k = m = n = 1.
b) ( ) 内はエチレンォキシド平均付加モル数を示し、 一般式 (3) の p = 2である化合物。  b) The compounds in parentheses indicate the average number of moles of ethylene oxide added, and p = 2 in the general formula (3).
c) ソフケア KG— 301 W;花王 (株) 製  c) Sofcare KG—301 W; manufactured by Kao Corporation
d) カーボポール E T D2020 ; B FGo o d r i c h社製 実施例 22 (洗顔料)  d) Carbopol E T D2020; manufactured by B FGoodric h Example 22 (face wash)
(成 分) (重量0 /o) ラウリルホスフエ一ト K塩 (Ingredient) (Weight 0 / o) Lauryl phosphate K salt
(モノラウリル体 ジラウリル体 = 75 25) 0. 5 ポリオキシエチレン (1 ) ラウリルエーテルホスフェート K塩 a)  (Monolauryl dilauryl = 75 25) 0.5 Polyoxyethylene (1) Lauryl ether phosphate K salt a)
(モノラウリル体 ジラウリル体 = 75 25) 1. 5 ポリオキシエチレン (1 ) ラウリル硫酸アンモニゥ厶 b) 24. 0 ジプロピレングリコール 1 0. 0 (Monolauryl dilauryl = 75 25) 1.5 Polyoxyethylene (1) Ammonium lauryl sulfate b) 24. 0 Dipropylene glycol 1 0. 0
2—ェチルへキシルグリセリルエーテル 0. 2 ラウロイルヒドロキシスルホべタイン 1. 2 N, N—ジメチルアミノエチルメタクリル酸ジェチル硫酸塩■ N, N- ジメチルァクリルアミ ド■ジメタクリル酸ポリエチレングリコール共 重合体 4重量%水溶液 G) 2. 5 アクリル酸メタクリル酸アルキル共重合体 d) 0. 5 塩化ナトリウム 1. 0 硫酸ナトリウム 3. 0 ジステアリン酸エチレングリコール 2. 0 メチルパラベン 0. 2 プロピルパラベン 0. 12-Ethylhexyl glyceryl ether 0.2 Lauroyl hydroxysulfobetaine 1.2 N, N-dimethylaminoethyl methacrylate ethyl methacrylate ■ N, N-dimethylacrylamide ■ Polyethylene glycol dimethacrylate copolymer 4 Weight% aqueous solution G) 2.5 Alkyl methacrylate copolymer d) 0.5 Sodium chloride 1. 0 Sodium sulfate 3. 0 Ethylene glycol distearate 2.0 Methyl paraben 0.2 Propropyl paraben 0.1
B H T 0. 2 香料 0. 05 精製水 バランス 計 1 00. 00 a) ( ) 内はエチレンォキシド平均付加モル数を示し、 一般式 (1 ) 及び (2) の k=m= n = 1である化合物。 BHT 0. 2 Fragrance 0. 05 Purified water balance total 1 00. 00 a) In (), the average number of moles added of ethylene oxide is shown, and in the formulas (1) and (2), k = m = n = 1.
b) ( ) 内はエチレンォキシド平均付加モル数を示し、 一般式 (3) の p= 1である化合物。  b) Compounds in () indicate the average number of added moles of ethylene oxide, and p = 1 in the general formula (3).
c) ソフケア KG— 301 W;花王 (株) 製  c) Sofcare KG—301 W; manufactured by Kao Corporation
d) カーボポール E T D2020 ; B FGo o d r i c h社製 実施例 23 (ボディシャンプー)  d) Carbopol E T D2020; B FGo o dric h Example 23 (Body shampoo)
(成 分) (重量%) ラウリルホスフエ一ト K塩  (Component) (wt%) Lauryl phosphate K salt
(モノラウリル体 ジラウリル体 = 75 25) 1. 3 ポリオキシエチレン (1 ) ラウリルエーテルホスフェート K塩 a)  (Monolauryl dilauryl = 75 25) 1.3 Polyoxyethylene (1) Lauryl ether phosphate K salt a)
(モノラウリル体 ジラウリル体 = 75 25) 3. 8 ポリオキシエチレン (2) ラウリルエーテル硫酸 N a b) 1 5. 0 ジプロピレングリコール 0. 7 ジプロピレングリコールモノォクチルエーテル 0. 6 ラウロイルヒドロキシスルホべタイン 1 0. 0 トリイソステアリン酸ポリオキシエチレンソルビタン  (Monolauryl dilauryl = 75 25) 3.8 Polyoxyethylene (2) Lauryl ether sulfate N ab) 1 5. 0 Dipropylene glycol 0.7 Dipropylene glycol monooctyl ether 0.6 Lauroyl hydroxysulfobetaine 1 0. 0 Polyoxyethylene sorbitan triisostearate
( 1 60 EO) 2. 0 ソルビット液 5. 0 N, N—ジメチルアミノエチルメタクリル酸ジェチル硫酸塩■ N, N- ジメチルァクリルアミ ド■ジメタクリル酸ポリエチレングリコール共 重合体 4重量%水溶液 G) 2. 5 ジステアリン酸エチレングリコール 2. 0 メチルパラベン 0. 1 プロピルパラベン 0. 2 (1 60 EO) 2.0 Sorbite solution 5.0 N, N-dimethylaminoethyl jetyl sulfate methacrylate N, N-dimethylacrylamide Polyethylene glycol dimethacrylate 4 wt% aqueous solution G) 2.5 Ethylene glycol distearate 2.0 Methyl paraben 0.1 Propropyl paraben 0.2
B H 0. 2 香料 0. 05 精製水 バランス 計 1 00. 00 a) ( ) 内はエチレンォキシド平均付加モル数を示し、 一般式 (1 ) 及び (2) の k=m= n = 1である化合物。 BH 0.2 Perfume 0. 05 Purified water Balance total 1 00. 00 a) () shows the average number of moles of ethylene oxide added, and in the general formulas (1) and (2), k = m = n = 1.
b) ( ) 内はエチレンォキシド平均付加モル数を示し、 一般式 (3) の p = 2である化合物。  b) The compounds in parentheses indicate the average number of moles of ethylene oxide added, and p = 2 in the general formula (3).
c) ソフケア KG— 301 W;花王 (株) 製  c) Sofcare KG—301 W; manufactured by Kao Corporation
実施例 24 (ボディシャンプー) Example 24 (body shampoo)
(成 分) (重量0 /o) ラウリルホスフエ一トトリエタノールアミン塩 (Ingredient) (Weight 0 / o) Lauryl phosphite triethanolamine salt
(モノラウリル体 ジラウリル体 =75 25) 1. 3 ポリオキシエチレン (1 ) ラウリルエーテルホスフェートトリエタノール アミン塩 a)  (Monolauryl dilauryl = 75 25) 1.3 Polyoxyethylene (1) Lauryl ether phosphate triethanol amine salt a)
(モノラウリル体 ジラウリル体 = 75Z 25) 3. 8 ポリオキシエチレン (2) ラウリルエーテル硫酸 N a b) 1 5. 0 ジプロピレングリコール 0. 7 ジエチレングリコール 2 _ェチルへキシルエーテル 0. 3 ラウロイルヒドロキシスルホべタイン 1 0. 0 トリイソステアリン酸ポリオキシエチレンソルビタン  (Monolauryl dilauryl = 75Z 25) 3. 8 Polyoxyethylene (2) Lauryl ether sulfate N ab) 1 5. 0 Dipropylene glycol 0.7 Diethylene glycol 2_ethylhexyl ether 0.3 Lauroyl hydroxysulfobetaine 1 0. 0 Polyoxyethylene sorbitan triisostearate
( 1 60 EO) 2. 0 ソルビット液 5. 0 N, N—ジメチルアミノエチルメタクリル酸ジェチル硫酸塩■ N, N- ジメチルァクリルアミ ド■ジメタクリル酸ポリエチレングリコール共 重合体 4重量%水溶液 C) 2. 5 ジステアリン酸エチレングリコール 2. 0 メチルパラベン 0. 1 プロピルパラベン 0. 2 B H T (1 60 EO) 2.0 Sorbite solution 5.0 N, N-dimethylaminoethyl jetyl sulfate methacrylate N, N-dimethylacrylamide Polyethylene glycol dimethacrylate 4 wt% aqueous solution C) 2.5 Ethylene glycol distearate 2.0 Methyl paraben 0.1 Propropyl paraben 0.2 BHT
香料 Fragrance
a) ( ) 内はエチレンォキシド平均付加モル数を示し、 一般式 (1 ) 及び (2) の k=m= n = 1である化合物。 a) In (), the average number of moles of ethylene oxide added is shown, and in the general formulas (1) and (2), k = m = n = 1.
b) ( ) 内はエチレンォキシド平均付加モル数を示し、 一般式 (3) の p = 2である化合物。  b) The compounds in parentheses indicate the average number of moles of ethylene oxide added, and p = 2 in the general formula (3).
c) ソフケア KG— 301 W;花王 (株) 製  c) Sofcare KG—301 W; manufactured by Kao Corporation

Claims

請求の範囲 次の成分 (A) 、 (B) 及び (C) (A) (31) —般式 (1 ) で表されるリン酸モノエステル系界面活性剤と (a 2) —般式 (2) で表されるリン酸ジエステル系界面活性剤 との混合物であって、 その含有比率が重量比で (ai) (a2) =90 1 0 〜50 50であるリン酸エステル系界面活性剤: Claims The following components (A), (B) and (C) (A) (31) —phosphate monoester surfactant represented by the general formula (1) and (a 2) —general formula ( 2) a phosphate ester surfactant represented by the following formula, the content ratio of which is (ai) (a2) = 90 10-5050:
[化 1] [Chemical 1]
Figure imgf000021_0001
Figure imgf000021_0001
(式中、 R1、 R2及び R3はそれぞれ炭素数 8〜 1 8の直鎖もしくは分岐鎖のァ ルキル基もしくはアルケニル基を示し、 X1、 X2、 Yはそれぞれ水素原子、 ァ ルカリ金属原子、 アルカリ土類金属原子、 アルカノールァミン又はアンモニ ゥムを示し、 平均付加モル数 k、 m及び nはそれぞれ 0〜1 0の数を示す) (In the formula, R 1 , R 2 and R 3 each represent a linear or branched alkyl group or alkenyl group having 8 to 18 carbon atoms, and X 1 , X 2 and Y represent a hydrogen atom and an alkali, respectively. A metal atom, an alkaline earth metal atom, an alkanolamine, or an ammonium, and the average number of moles added, k, m, and n are each 0 to 10)
(B) —般式 (3) (B) — General formula (3)
R 0 (C H2C H20) PS 03M (3) R 0 (CH 2 CH 2 0) P S 0 3 M (3)
(式中 R4は炭素数 8〜 1 8のアルキル基もしくはアルケニル基を示し、 は アルカリ金属原子、 アルカリ土類金属原子、 アルカノールァミン、 アンモニ ゥム又は塩基性アミノ酸を示し、 平均付加モル数 pは 0〜 5の数を示す。 ) で表される硫酸エステル系界面活性剤; (Wherein R 4 represents an alkyl group or alkenyl group having 8 to 18 carbon atoms, represents an alkali metal atom, alkaline earth metal atom, alkanolamine, ammonium or basic amino acid, and the average number of moles added. p represents a number from 0 to 5. A sulfate ester surfactant represented by:
(C) (C- 1 ) 炭素数 6~1 2の直鎖もしくは分岐鎖のアルキル基もし くはアルケニル基を有する 1種以上のグリセリルエーテル、 及び  (C) (C-1) one or more glyceryl ethers having a linear or branched alkyl or alkenyl group having 6 to 12 carbon atoms, and
(C-2) —般式 (4)  (C-2) — General formula (4)
RsO (AO) qR6 (4) R s O (AO) q R 6 (4)
(式中、 R5は炭素数 6〜 1 0の直鎖もしくは分岐鎖のアルキル基もしくはァ ルケ二ル基を示し、 R6は水素原子又はメチル基を示し、 A Oは炭素数 2〜 4 のアルキレンォキシ基を示し、 平均付加モル数 qは 0. 5~3の数を示す。(In the formula, R 5 represents a linear or branched alkyl group having 6 to 10 carbon atoms or R 6 represents a rukenyl group, R 6 represents a hydrogen atom or a methyl group, AO represents an alkyleneoxy group having 2 to 4 carbon atoms, and the average added mole number q represents a number of 0.5 to 3.
) )
で表される化合物から選ばれる 1種以上;  One or more selected from the compounds represented by:
を含有する洗浄剤組成物。  A cleaning composition comprising:
[2] 成分 (A) と成分 (B) の含有比率が重量比で成分 (B) 成分 (A) = [2] The content ratio of component (A) to component (B) is the weight ratio of component (B) component (A) =
1〜 1 0である請求項 1記載の洗浄剤組成物。  The cleaning composition according to claim 1, which is 1 to 10.
[3] 成分 (A) が 1〜1 5重量%である請求項 1又は 2記載の洗浄剤組成物。 [3] The cleaning composition according to claim 1 or 2, wherein the component (A) is 1 to 15% by weight.
[4] 成分 (B) が 5〜40重量%である請求項 1〜3の何れか 1項記載の洗浄 剤組成物。 [4] The cleaning composition according to any one of claims 1 to 3, wherein the component (B) is 5 to 40% by weight.
[5] 成分 (C) が 0. 1〜20重量%である請求項 1〜4の何れか 1項記載の 洗浄剤組成物。  [5] The cleaning composition according to any one of claims 1 to 4, wherein the component (C) is 0.1 to 20% by weight.
[6] p H 4-8である請求項 1 ~ 5の何れか 1項記載の洗浄剤組成物。  [6] The detergent composition according to any one of claims 1 to 5, which has a pH of 4-8.
[7] 硬度が 1 ~30° DHの水と共に用いられるものである請求項 1 ~ 6の何 れか 1項記載の洗浄剤組成物。  [7] The cleaning composition according to any one of [1] to [6], which is used together with water having a hardness of 1 to 30 ° DH.
[8] p Hが 4 ~ 9である水と共に用いられるものである請求項 1 ~ 7の何れか [8] The method according to any one of claims 1 to 7, wherein the pH is used together with water having a pH of 4 to 9.
1項記載の洗浄剤組成物。  The cleaning composition according to claim 1.
[9] 請求項 1 ~ 8の何れか 1項記載の洗浄剤組成物を身体に適用する身体の洗 浄方法。 [9] A method for cleaning the body, wherein the cleaning composition according to any one of claims 1 to 8 is applied to the body.
[10] 請求項 1 ~ 8の何れか 1項記載の洗浄剤組成物の身体の洗浄への使用。  [10] Use of the cleaning composition according to any one of claims 1 to 8 for washing the body.
PCT/JP2007/000375 2006-04-07 2007-04-06 Cleansing composition WO2007116586A1 (en)

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JP2009275009A (en) * 2008-05-16 2009-11-26 Kao Corp Skin cleanser composition
JP2009275010A (en) * 2008-05-16 2009-11-26 Kao Corp Skin cleanser composition
JP2009275012A (en) * 2008-05-16 2009-11-26 Kao Corp Skin cleanser composition
WO2011158483A1 (en) * 2010-06-18 2011-12-22 花王株式会社 Aqueous hair cleansing agent

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Publication number Priority date Publication date Assignee Title
JP5730507B2 (en) 2010-07-08 2015-06-10 花王株式会社 Hair cosmetics

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JPH03285996A (en) * 1990-04-02 1991-12-17 Kao Corp Detergent composition
JP2004168951A (en) * 2002-11-21 2004-06-17 Kao Corp Detergent composition
JP2005206804A (en) * 2003-12-26 2005-08-04 Kao Corp Detergent composition
JP2006022116A (en) * 2003-04-14 2006-01-26 Kao Corp Detergent composition

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JP3093981B2 (en) * 1996-04-05 2000-10-03 花王株式会社 Detergent composition
US20060142174A1 (en) * 2003-04-14 2006-06-29 Kao Corporation Cleaning agent composition
US7183244B2 (en) * 2003-12-26 2007-02-27 Kao Corporation Detergent compositions comprising a mixture of phosphate esters

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JPH03285996A (en) * 1990-04-02 1991-12-17 Kao Corp Detergent composition
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JP2006022116A (en) * 2003-04-14 2006-01-26 Kao Corp Detergent composition
JP2005206804A (en) * 2003-12-26 2005-08-04 Kao Corp Detergent composition

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2009275009A (en) * 2008-05-16 2009-11-26 Kao Corp Skin cleanser composition
JP2009275010A (en) * 2008-05-16 2009-11-26 Kao Corp Skin cleanser composition
JP2009275012A (en) * 2008-05-16 2009-11-26 Kao Corp Skin cleanser composition
WO2011158483A1 (en) * 2010-06-18 2011-12-22 花王株式会社 Aqueous hair cleansing agent
US8530398B2 (en) 2010-06-18 2013-09-10 Kao Corporation Aqueous hair cleansing agent
TWI465255B (en) * 2010-06-18 2014-12-21 Kao Corp Aqueous hair cleansing composition

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