JP2013139439A - Skin cleansing agent composition - Google Patents

Skin cleansing agent composition Download PDF

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JP2013139439A
JP2013139439A JP2012268092A JP2012268092A JP2013139439A JP 2013139439 A JP2013139439 A JP 2013139439A JP 2012268092 A JP2012268092 A JP 2012268092A JP 2012268092 A JP2012268092 A JP 2012268092A JP 2013139439 A JP2013139439 A JP 2013139439A
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JP5349674B2 (en
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Junko Sonoda
純子 園田
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Kao Corp
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    • 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
    • A61K8/19Cosmetics or similar toiletry preparations characterised by the composition containing inorganic ingredients
    • 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
    • A61K8/36Carboxylic acids; Salts or anhydrides thereof
    • A61K8/361Carboxylic acids having more than seven carbon atoms in an unbroken chain; Salts or anhydrides thereof
    • 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
    • A61K8/72Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/81Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
    • A61K8/817Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a single or double bond to nitrogen or by a heterocyclic ring containing nitrogen; Compositions or derivatives of such polymers, e.g. vinylimidazol, vinylcaprolactame, allylamines (Polyquaternium 6)
    • 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
    • C11D1/008Polymeric surface-active agents
    • 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
    • C11D1/04Carboxylic acids or salts thereof
    • 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
    • C11D1/04Carboxylic acids or salts thereof
    • C11D1/06Ether- or thioether carboxylic acids
    • 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
    • C11D1/38Cationic compounds
    • C11D1/65Mixtures of anionic with cationic 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
    • C11D10/00Compositions of detergents, not provided for by one single preceding group
    • C11D10/04Compositions of detergents, not provided for by one single preceding group based on mixtures of surface-active non-soap compounds and soap
    • C11D10/042Compositions of detergents, not provided for by one single preceding group based on mixtures of surface-active non-soap compounds and soap based on anionic surface-active compounds and soap

Abstract

PROBLEM TO BE SOLVED: To provide a skin cleansing agent composition which materializes fine foam quality with excellent elasticity and skin with a moist feeling and without stiffness after finishing of washing.SOLUTION: The skin cleansing agent composition contains: (A) 1 to 20 mass% of alkyl ether carboxylic acids represented by general formula (1) (in formula, Rrepresents a 4-22C alkyl group, and n represents a number from 0 to 20), wherein the average number of carbon atoms in Ris 10.8 to 12.8, the content of components in which n=0 is 4.3 to 30 mass%, and the total content of components in which n=1 and components in which n=2 is at least 20 mass% and less than 40 mass%; (B) 1 to 20 mass% of a straight chain or branched chain 10-22C fatty acids; (C) 0.1 to 5 mass% of a cationic polymer; (D) a base; and (E) water. At least a part of the component (A) and a part of the component (B) are present in the form of salts with the component (D), and a molar ratio of the component (D) relative to the component (A) and the component (B) (component (D))/(component (A)+component (B)) is 0.9 to 1.1.

Description

本発明は、皮膚洗浄剤組成物に関する。   The present invention relates to a skin cleansing composition.

近年、身体洗浄剤には、皮膚へのやさしさが求められている。特に、洗浄時の泡について、弾力性のないキメの粗い泡で摩擦のある洗浄を続けると、肌の乾燥や、しみ、しわなどといった肌トラブルを引き起こすと考える消費者もおり、アンチエイジング意識の高まりとともに、より弾力性のある泡が得られる洗浄剤が求められている。   In recent years, body cleansing agents are required to be gentle on the skin. In particular, with regard to foam during washing, some consumers believe that continuing to wash with friction with rough, non-elastic foam will cause skin problems such as dry skin, spots and wrinkles. Along with the increase, there is a need for a detergent that can provide more elastic foam.

弾力性のある泡が得られると考えられている洗浄剤の1つに、脂肪酸を晶析させたペースト状の洗浄剤が挙げられる。特許文献1では、脂肪酸とカチオン性高分子の組み合わせが開示されている。   One of the cleaning agents that are considered to obtain elastic foam is a paste-like cleaning agent in which fatty acids are crystallized. Patent Document 1 discloses a combination of a fatty acid and a cationic polymer.

また、泡に弾力性を出すために、アニオン界面活性剤と特定の非イオン界面活性剤を組み合わせ、泡膜を強化する方法(特許文献2)、特定の脂肪酸塩と他の界面活性剤を組み合わせことにより、均質でクリーミィーな泡質を形成させることが試みられている(特許文献3)。   Moreover, in order to give elasticity to the foam, a combination of an anionic surfactant and a specific nonionic surfactant to strengthen the foam film (Patent Document 2), a specific fatty acid salt and another surfactant are combined. Thus, attempts have been made to form a homogeneous and creamy foam (Patent Document 3).

特開2011−20941号公報JP 2011-20941 A 特開2008−150303号公報JP 2008-150303 A 特開平11−35972号公報JP-A-11-35972

特許文献1のように脂肪酸を晶析させたペースト状の洗浄剤は、多量の脂肪酸を必要とし、洗浄後の使用感として、つっぱり感、乾燥感が出やすく、人によっては好まれない場合がある。一方、特許文献2のようにアニオン界面活性剤と特定の非イオン界面活性剤の組み合わせや、特許文献3のように脂肪酸塩と他の界面活性剤の組み合わせでは、クリーミーな泡質を形成させるものの、泡の弾力性は弱くなってしまうという課題がある。
本発明は、泡質がキメ細かく弾力性に優れ、洗い上がりの肌がしっとりしてつっぱり感が抑制された皮膚洗浄剤組成物に関する。
The paste-like cleaning agent crystallized with fatty acid as in Patent Document 1 requires a large amount of fatty acid, and as a feeling of use after cleaning, it tends to give a feeling of tension and dryness, and may not be preferred by some people. is there. On the other hand, a combination of an anionic surfactant and a specific nonionic surfactant as in Patent Document 2 or a combination of a fatty acid salt and another surfactant as in Patent Document 3 forms a creamy foam. There is a problem that the elasticity of bubbles is weakened.
The present invention relates to a skin cleanser composition having fine foam quality, excellent elasticity, and moisturized skin and a reduced feeling of tension.

本発明者は、特定のアルキルエーテルカルボン酸と、特定の脂肪酸、カチオンポリマーとを組み合わせて用いれば、泡質がキメ細かく弾力性に優れ、且つ洗い上がりの肌がしっとりして、つっぱり感が抑制された皮膚洗浄剤組成物が得られることを見出した。   When the present inventor uses a combination of a specific alkyl ether carboxylic acid, a specific fatty acid and a cationic polymer, the foam quality is fine and excellent in elasticity, and the washed-out skin is moist and the feeling of tension is suppressed. It was found that a skin cleansing composition was obtained.

本発明は、次の成分(A)、(B)、(C)、(D)及び(E):
(A)一般式(1)
The present invention includes the following components (A), (B), (C), (D) and (E):
(A) General formula (1)

Figure 2013139439
Figure 2013139439

(式中、R1は炭素数4〜22のアルキル基を示し、nは0〜20の数を示す)
で表されるアルキルエーテルカルボン酸であって、R1の平均炭素数が10.8〜12.8であり、n=0の成分を4.3〜30質量%含み、n=1の成分とn=2の成分の合計含有量が20質量%以上40質量%未満であるアルキルエーテルカルボン酸 1〜20質量%、
(B)一般式(2)
(In the formula, R 1 represents an alkyl group having 4 to 22 carbon atoms, and n represents a number of 0 to 20).
Wherein R 1 has an average carbon number of 10.8 to 12.8, 4.3 to 30% by mass of n = 0, and n = 1 1-20% by mass of an alkyl ether carboxylic acid having a total content of n = 2 components of 20% by mass or more and less than 40% by mass,
(B) General formula (2)

Figure 2013139439
Figure 2013139439

(式中、R2は炭素数9〜21の直鎖又は分岐鎖のアルキル基又はアルケニル基を示す)
で表される脂肪酸 1〜20質量%、
(C)カチオンポリマー 0.1〜5質量%、
(D)塩基、
(E)水
を含有し、成分(A)及び(B)は、少なくとも一部が成分(D)と塩で存在し、成分(D)は、成分(A)及び(B)に対するモル比(成分(D)/(成分(A)+成分(B))が0.9〜1.1である皮膚洗浄剤組成物に関する。
(Wherein R 2 represents a linear or branched alkyl or alkenyl group having 9 to 21 carbon atoms)
1 to 20% by mass of a fatty acid represented by
(C) Cationic polymer 0.1-5% by mass,
(D) a base,
(E) It contains water, and components (A) and (B) are at least partially present as component (D) and salt, and component (D) is a molar ratio of components (A) and (B) ( It is related with the skin cleansing composition whose component (D) / (component (A) + component (B)) is 0.9-1.1.

本発明の皮膚洗浄剤組成物は、泡質がキメ細かく弾力性に優れ、且つ洗い上がりの肌がしっとりしてつっぱり感が抑制されているものである。本発明において、つっぱり感とは、洗い上がりのとき、例えばタオルドライをした後に、皮膚の表面がひっぱられているような感覚である。   The skin cleanser composition of the present invention has a fine foam quality and excellent elasticity, and the washed-out skin is moist and the feeling of tension is suppressed. In the present invention, the feeling of tension is a feeling that the surface of the skin is pulled after washing, for example, after towel drying.

本発明で用いる成分(A)のアルキルエーテルカルボン酸は、一般式(1)で表されるものである。
式中、R1は炭素数4〜22のアルキル基であり、炭素数6〜20のアルキル基、更に炭素数8〜18のアルキル基、更には炭素数8〜16のアルキル基が好ましく、炭素数10〜16のアルキル基がより好ましい。また、R1のアルキル鎖は、直鎖又は分岐鎖のいずれでも良いが、起泡性の点から、直鎖アルキル基が好ましい。また、R1の平均炭素数は10.8〜12.8であり、好ましくは10.8〜12.5、より好ましくは12.1〜12.4である。この範囲内であれば、起泡性及び泡質、さらに低温安定性の点で優れるので好ましい。
また、R1は2種以上のアルキル基を含むことが好ましく、一番含有量の多いアルキル鎖長を有する成分が55質量%以上97質量%未満であるのが好ましく、60〜95質量%がより好ましく、さらに70〜95質量%であるのが、泡量及び泡質に優れるので好ましい。
The alkyl ether carboxylic acid of component (A) used in the present invention is represented by the general formula (1).
In the formula, R 1 is an alkyl group having 4 to 22 carbon atoms, preferably an alkyl group having 6 to 20 carbon atoms, further an alkyl group having 8 to 18 carbon atoms, and more preferably an alkyl group having 8 to 16 carbon atoms. An alkyl group of several 10 to 16 is more preferable. The alkyl chain of R 1 may be either a straight chain or a branched chain, but a straight chain alkyl group is preferred from the viewpoint of foamability. R 1 has an average carbon number of 10.8 to 12.8, preferably 10.8 to 12.5, and more preferably 12.1 to 12.4. If it is in this range, it is excellent in terms of foamability and foam quality, and stability at low temperature, which is preferable.
R 1 preferably contains two or more alkyl groups, and the component having the largest alkyl chain length is preferably 55% by mass or more and less than 97% by mass, and 60 to 95% by mass. More preferably, it is preferably 70 to 95% by mass because the foam amount and foam quality are excellent.

また、式中、nは0〜20の数を示し、0〜12がより好ましい。なお、nは、エチレンオシキシドの付加モル数を示し、成分(A)の組成中の平均付加モル数(nの平均値)は、泡質が良好である点から、1.5〜10が好ましく、2.5〜4.5がより好ましく、さらに2.5〜3.4が好ましく、2.8〜3.4がより好ましく、さらに2.8〜3.1がより好ましい。
成分(A)のアルキルエーテルカルボン酸は、一般式(1)において、n=0の成分を4.3〜30質量%含み、4.9〜27質量%が好ましく、9.6〜27質量%がより好ましく、9.9〜16質量%が更に好ましく、9.9〜15質量%含むのがより更に好ましい。この範囲内とすることにより、すすぎ時のきしみ感が向上する。
さらに、n=1の成分とn=2の成分の合計含有量が20質量%以上40質量%未満であり、泡質、泡量の観点から、好ましくは20〜37質量%、より好ましくは27〜36.5質量%、更に好ましくは35〜36.1質量%である。
Moreover, in formula, n shows the number of 0-20, and 0-12 are more preferable. In addition, n shows the addition mole number of ethylene oxyoxide, and the average addition mole number (average value of n) in the composition of a component (A) is 1.5-10 from the point that foam quality is favorable. Preferably, 2.5 to 4.5 is more preferable, 2.5 to 3.4 is more preferable, 2.8 to 3.4 is more preferable, and 2.8 to 3.1 is more preferable.
In the general formula (1), the alkyl ether carboxylic acid of the component (A) includes 4.3 to 30% by mass of the component of n = 0, preferably 4.9 to 27% by mass, and 9.6 to 27% by mass. Is more preferable, 9.9-16 mass% is still more preferable, and it is still more preferable to contain 9.9-15 mass%. By making it within this range, the squeaky feeling at the time of rinsing is improved.
Furthermore, the total content of the component of n = 1 and the component of n = 2 is 20% by mass or more and less than 40% by mass, and preferably 20 to 37% by mass, more preferably 27 from the viewpoint of foam quality and foam amount. It is -36.5 mass%, More preferably, it is 35-36.1 mass%.

成分(A)のアルキルエーテルカルボン酸は、一般式(1)中、n=0、1、2、3、4の成分の質量割合が、(n=0成分の質量):(n=1成分の質量):(n=2成分の質量):(n=3成分の質量):(n=4成分の質量)=1:0.99〜3.50:0.89〜3.00:0.76〜3.00:0.63〜1.6であることが、起泡性、洗浄性、すすぎ時のきしみ感の両立性の点から好ましい。   In the general formula (1), the component (A) alkyl ether carboxylic acid has a mass ratio of components of n = 0, 1, 2, 3, and 4 (n = 0 component mass): (n = 1 component) Mass): (mass of n = 2 components): (mass of n = 3 components): (mass of n = 4 components) = 1: 0.99 to 3.50: 0.89 to 3.00: 0 .76 to 3.00: 0.63 to 1.6 is preferable from the viewpoint of compatibility between foamability, detergency, and squeaky feeling during rinsing.

さらには、一般式(1)中、n=0の成分を9.6質量%以上12質量%未満含み、(n=0成分の質量):(n=1成分の質量):(n=2成分の質量):(n=3成分の質量):(n=4成分の質量)=1:1.53〜1.87:1.59〜2.25:1.33〜2.16:1.14〜1.52となるか、又は、n=0の成分を12質量%以上17質量%以下含み、(n=0成分の質量):(n=1成分の質量):(n=2成分の質量):(n=3成分の質量):(n=4成分の質量)=1:0.99〜1.34:0.89〜1.40:0.76〜1.23:0.63〜0.99となるのが、起泡性とすすぎ性の観点から好ましい。   Furthermore, in general formula (1), the component of n = 0 is contained 9.6 mass% or more and less than 12 mass%, (mass of n = 0 component) :( mass of n = 1 component) :( n = 2 Component mass): (n = 3 component mass): (n = 4 component mass) = 1: 1.53-1.87: 1.59-2.25: 1.33-2.16: 1 .14 to 1.52, or 12 to 17% by mass of n = 0 component, (n = 0 component mass): (n = 1 component mass): (n = 2 Component mass): (n = 3 component mass): (n = 4 component mass) = 1: 0.99 to 1.34: 0.89 to 1.40: 0.76 to 1.23: 0 .63 to 0.99 is preferable from the viewpoint of foaming properties and rinsing properties.

さらに、一般式(1)中、n=0の成分を9.9〜11.5質量%含み、(n=0成分の質量):(n=1成分の質量):(n=2成分の質量):(n=3成分の質量):(n=4成分の質量)=1:1.58〜1.84:1.72〜2.17:1.49〜2.00:1.14〜1.52となるか、又は、一般式(1)中、n=0の成分を13〜17質量%含み、(n=0成分の質量):(n=1成分の質量):(n=2成分の質量):(n=3成分の質量):(n=4成分の質量)=1:1.00〜1.31:0.93〜1.34:0.79〜1.18:0.63〜0.99となるのが、泡量、泡質とすすぎ性の観点から好ましい。   Further, in the general formula (1), the component of n = 0 is included in the range of 9.9 to 11.5% by mass, (the mass of the n = 0 component): (the mass of the n = 1 component): (the n = 2 component) Mass): (mass of n = 3 components): (mass of n = 4 components) = 1: 1.58-1.84: 1.72-2.17: 1.49-2.00: 1.14 To 1.52 or, in the general formula (1), 13 to 17% by mass of n = 0 component, (n = 0 component mass): (n = 1 component mass): (n = Mass of 2 components) :( mass of n = 3 components) :( mass of 4 components) = 1: 1.00 to 1.31: 0.93 to 1.34: 0.79 to 1.18 : 0.63 to 0.99 is preferable from the viewpoints of the amount of foam, foam quality and rinsing properties.

成分(A)において、一般式(1)中、R1は炭素数4〜22のアルキル基であり、R1の平均炭素数は10.8〜12.8であり、また、一番含有量の多いアルキル鎖長を有する成分が55質量%以上97質量%未満であり、更に、nは0〜20の数を示し、平均値は、1.5〜10であり、n=0の成分を4.9〜27質量%含み、n=1の成分とn=2の成分の合計含有量が20〜37質量%であることが好ましい。このようにすることで、起泡性を早めることができる。 In the component (A), in the general formula (1), R 1 is an alkyl group having 4 to 22 carbon atoms, the average carbon number of R 1 is 10.8 to 12.8, and the most content The component having a large alkyl chain length is 55% by mass or more and less than 97% by mass, n represents a number of 0 to 20, the average value is 1.5 to 10, and the component of n = 0 It is preferable that the total content of the component of n = 1 and the component of n = 2 is 20-37 mass% including 4.9-27 mass%. By doing in this way, foamability can be accelerated.

成分(A)において、一般式(1)中、R1は炭素数6〜20のアルキル基であり、R1の平均炭素数は10.8〜12.8であり、また、一番含有量の多いアルキル鎖長を有する成分が55質量%以上97質量%未満であり、更に、nは0〜20の数を示し、平均値は、2.5〜4.5であり、n=0の成分を9.6〜27質量%含み、n=1の成分とn=2の成分の合計含有量が27〜36.5質量%であることが好ましい。このようにすることで、起泡性を早めることができる。 In the component (A), in the general formula (1), R 1 is an alkyl group having 6 to 20 carbon atoms, and the average carbon number of R 1 is 10.8 to 12.8. The component having a large alkyl chain length is 55% by mass or more and less than 97% by mass, n represents a number of 0 to 20, an average value is 2.5 to 4.5, and n = 0. It is preferable that a component is contained 9.6-27 mass%, and the sum total content of the component of n = 1 and the component of n = 2 is 27-36.5 mass%. By doing in this way, foamability can be accelerated.

成分(A)において、一般式(1)中、R1は炭素数8〜18のアルキル基であり、R1の平均炭素数は10.8〜12.8であり、また、一番含有量の多いアルキル鎖長を有する成分が55質量%以上97質量%未満であり、更に、nは0〜20の数を示し、平均値は、2.5〜3.4であり、n=0の成分を9.6〜27質量%含み、n=1の成分とn=2の成分の合計含有量が27〜36.5質量%であることが好ましい。このようにすることで、すすぎ時のストップフィーリング性を強めることができる。 In the component (A), in the general formula (1), R 1 is an alkyl group having 8 to 18 carbon atoms, the average carbon number of R 1 is 10.8 to 12.8, and the most content The component having a large alkyl chain length is 55% by mass or more and less than 97% by mass, n represents a number of 0 to 20, an average value is 2.5 to 3.4, and n = 0. It is preferable that a component is contained 9.6-27 mass%, and the sum total content of the component of n = 1 and the component of n = 2 is 27-36.5 mass%. By doing in this way, the stop feeling property at the time of a rinse can be strengthened.

成分(A)において、一般式(1)中、R1は炭素数8〜16のアルキル基であり、R1の平均炭素数は10.8〜12.5であり、また、一番含有量の多いアルキル鎖長を有する成分が60〜95質量%であり、更に、nは0〜20の数を示し、平均値は、2.8〜3.4であり、n=0の成分を9.6〜27質量%、好ましくは9.9〜16質量%含み、n=1の成分とn=2の成分の合計含有量が27〜36.5質量%であるのが好ましい。このようにすることで、泡量、泡質を向上させることができる。 In the component (A), in the general formula (1), R 1 is an alkyl group having 8 to 16 carbon atoms, the average carbon number of R 1 is 10.8 to 12.5, and the most content The component having a large alkyl chain length is 60 to 95% by mass, n represents a number of 0 to 20, the average value is 2.8 to 3.4, and the component of n = 0 is 9 It is preferable that the total content of the component of n = 1 and the component of n = 2 is 27 to 36.5% by mass, including 6.6 to 27% by mass, preferably 9.9 to 16% by mass. By doing in this way, foam amount and foam quality can be improved.

成分(A)において、一般式(1)中、R1は炭素数10〜16のアルキル基であり、R1の平均炭素数は12.1〜12.4であり、また、一番含有量の多いアルキル鎖長を有する成分が60〜95質量%であり、更に、nは0〜20の数を示し、平均値は、2.8〜3.1であり、n=0の成分を9.9〜15質量%含み、n=1の成分とn=2の成分の合計含有量が35〜36.1質量%であるのが好ましい。このようにすることで、泡量、泡質、および泡の垂れにくさを向上させることができる。 In the component (A), in the general formula (1), R 1 is an alkyl group having 10 to 16 carbon atoms, the average carbon number of R 1 is 12.1 to 12.4, and the most content The component having a large alkyl chain length is 60 to 95% by mass, n represents a number of 0 to 20, the average value is 2.8 to 3.1, and the component of n = 0 is 9 It is preferable that the total content of the component of n = 1 and the component of n = 2 is 35 to 36.1% by mass. By doing in this way, the amount of foam, foam quality, and the difficulty of dripping can be improved.

なお、本発明の成分(A)において、R1のアルキル鎖長の分布、R1の平均アルキル鎖長、n=0の成分量、nの平均付加モル数、n=0、1、2、3、4の成分の質量割合は、一般式(1)で表されるアルキルエーテルカルボン酸をガスクロマトグラフィーによる分析を行い、以下のようにして求める。 Incidentally, in the components of the present invention (A), the distribution of alkyl chain length of R 1, the average alkyl chain length of R 1, components of n = 0, average addition mole number of n, n = 0, 1, 2, The mass ratio of the components 3 and 4 is determined as follows by analyzing the alkyl ether carboxylic acid represented by the general formula (1) by gas chromatography.

〔R1のアルキル鎖長の分布〕
ガスクロマトグラフィーより得られるピーク面積のうち、n=0モルに相当する各アルキル鎖長のピーク面積を求め、それらの総和を100とし、各アルキル鎖長分布の百分率を求めた。n=1〜3モルにおいても同様に計算し、n=0〜3モルの各アルキル鎖長分布の百分率の値を平均し、R1のアルキル鎖長の分布を求めた(これより、R1の組成のうち最も多く含有するアルキル基成分を特定できる)。
[Distribution of alkyl chain length of R 1 ]
Of the peak areas obtained by gas chromatography, the peak area of each alkyl chain length corresponding to n = 0 mol was determined, and the sum of these was determined as 100, and the percentage of each alkyl chain length distribution was determined. also calculated similarly in n = 1 to 3 mol, and the average value of the percentage of each alkyl chain length distribution of n = 0 to 3 mol, determined the distribution of alkyl chain length of R 1 (from which, R 1 The alkyl group component containing the largest amount of the composition can be specified).

〔R1の平均アルキル鎖長〕
上記のようにして求めたR1のアルキル鎖長の分布より、各成分の割合を求め、得られた割合に対応するアルキル鎖長分の炭素数を各々掛け、これらの総和を得た。これを平均アルキル鎖長とした。
[Average alkyl chain length of R 1 ]
From the distribution of the alkyl chain length of R 1 determined as described above, the ratio of each component was determined, and the carbon number corresponding to the alkyl chain length corresponding to the ratio thus obtained was multiplied to obtain the sum of these. This was defined as the average alkyl chain length.

〔n=0の成分量、n=1の成分とn=2の成分の合計含有量〕
1の組成のうち、最も多く含有するアルキル鎖長を特定し、その成分のn=0〜10に相当するガスクロマトグラフィーの面積を合計した。その合計量を100%として、n=0の成分量、n=1の成分とn=2の成分の合計含有量を算出した。
[Component content of n = 0, total content of component of n = 1 and component of n = 2]
Among the compositions of R 1 , the most abundant alkyl chain length was specified, and the areas of gas chromatography corresponding to n = 0 to 10 of the components were totaled. The total amount was 100%, and the total content of n = 0, n = 1 and n = 2 was calculated.

〔nの平均付加モル数〕
1の組成のうち最も多く含有するアルキル鎖長を特定し、その成分のn=0〜10に相当するガスクロマトグラフィーの面積を合計した(nが11以上のものは微量であり、計算から除いた)。その合計量を1として、n=0〜10の各々の割合を求めた。この割合に、各々の付加モル数を掛け、これらの合計をnの平均付加モル数とした。
[Average number of moles of n added]
The most alkyl chain length contained in the composition of R 1 was specified, and the areas of the gas chromatography corresponding to n = 0 to 10 of the components were totaled (the ones with n of 11 or more are trace amounts. Excluded). The total amount was set to 1, and the ratio of each of n = 0 to 10 was obtained. This ratio was multiplied by the number of moles added, and the sum of these was taken as the average number of moles added.

〔n=0、n=1、n=2、n=3、n=4の成分の質量割合〕
EO付加モル数の異なる各成分の比率に関しては、ガスクロマトグラフィーにより得られるピーク面積から、上記に示した方法でR1のアルキル鎖長の分布を求め、R1の組成のうち最大含有量のアルキル鎖長成分を特定し、その最大成分のn=0、n=1、n=2、n=3、n=4の面積比から特定した。
[Mass ratio of components of n = 0, n = 1, n = 2, n = 3, n = 4]
Regarding the ratio of each component having a different number of EO addition moles, the distribution of the alkyl chain length of R 1 is obtained from the peak area obtained by gas chromatography by the method described above, and the maximum content of the R 1 composition is determined. The alkyl chain length component was identified, and the maximum component was identified from the area ratio of n = 0, n = 1, n = 2, n = 3, and n = 4.

成分(A)のアルキルエーテルカルボン酸は、前記のような組成を有するもので、洗浄時の十分な泡量、良好な泡質を得つつ、つっぱり感を抑制する点から、全組成中に1質量%以上含有し、好ましくは5質量%以上含有し、更には6質量%以上含有することが好ましい。また、成分(A)の含有量は、全組成中に20質量%以下が好ましく、より好ましくは15質量%以下であり、更には12質量%以下が好ましい。また、成分(A)は、全組成中に1〜20質量%含有するのが好ましく、2〜15質量%がより好ましく、更に、4〜12質量%含有されるのが好ましい。なお、成分(A)は、成分(D)により、一部又は全部が塩を形成することにより、以上の効果を発現することができる。   The alkyl ether carboxylic acid of component (A) has the composition as described above. From the viewpoint of suppressing the feeling of sticking while obtaining a sufficient amount of foam at the time of washing and good foam quality, 1 in the total composition. It is contained in an amount of not less than 5% by mass, preferably not less than 5% by mass, and more preferably not less than 6% by mass. Further, the content of the component (A) is preferably 20% by mass or less, more preferably 15% by mass or less, and further preferably 12% by mass or less in the entire composition. Moreover, it is preferable to contain 1-20 mass% of components (A) in the whole composition, 2-15 mass% is more preferable, Furthermore, it is preferable that 4-12 mass% is contained. In addition, a component (A) can express the above effect, when a part or all forms a salt by a component (D).

本発明で用いる成分(B)の脂肪酸は、前記一般式(2)で表されるものである。
式中、R2は炭素数9〜21のアルキル基又はアルケニル基であり、直鎖又は分岐鎖のいずれでも良く、炭素数11〜21のアルキル基がより好ましく、更に炭素数13〜17のアルキル基が好ましい。
成分(B)としては、ミリスチン酸、パルミチン酸、ステアリン酸又はべヘン酸が好ましい。
The fatty acid of component (B) used in the present invention is represented by the general formula (2).
In the formula, R 2 is an alkyl group or alkenyl group having 9 to 21 carbon atoms, which may be linear or branched, more preferably an alkyl group having 11 to 21 carbon atoms, and further an alkyl group having 13 to 17 carbon atoms. Groups are preferred.
As the component (B), myristic acid, palmitic acid, stearic acid or behenic acid is preferable.

また、成分(B)の脂肪酸において、一般式(2)中、R2の炭素数が15〜21のアルキル基又はアルケニル基である脂肪酸が、成分(B)の全脂肪酸中に好ましくは40〜100質量%、更に好ましくは50〜80質量%含まれているのが、泡のキメをより細かくし、つっぱり感を抑制する点から好ましい。 Moreover, in the fatty acid of the component (B), in the general formula (2), the fatty acid which is an alkyl group or alkenyl group having 15 to 21 carbon atoms in R 2 is preferably 40 to 40 in the total fatty acid of the component (B). The content of 100% by mass, more preferably 50-80% by mass, is preferable from the viewpoint of making the texture of the foam finer and suppressing the feeling of tension.

成分(B)は、1種又は2種以上を用いることができ、洗浄性と起泡性を得る観点から、全組成中に1質量%以上含有し、好ましくは5質量%以上であり、更には6質量%以上が好ましい。また、成分(B)の全組成中の含有量は、泡の弾力性とつっぱり感の抑制の両立及び組成物の粘度等による泡立てやすさの点から20質量%以下が好ましく、より好ましくは15質量%以下であり、更には12質量%が好ましい。また、成分(B)は全組成中に1〜20質量%含有するのが好ましく、5〜15質量%がより好ましく、更に、6〜12質量%含有するのが好ましい。   Component (B) can be used singly or in combination of two or more, and from the viewpoint of obtaining detergency and foamability, it is contained in an amount of 1% by mass or more, preferably 5% by mass or more, Is preferably 6% by mass or more. In addition, the content of the component (B) in the total composition is preferably 20% by mass or less, more preferably 15% from the viewpoint of coexistence of foam elasticity and suppression of the feeling of tension and ease of foaming due to the viscosity of the composition. It is not more than mass%, and more preferably 12 mass%. Moreover, it is preferable to contain 1-20 mass% of components (B) in the whole composition, 5-15 mass% is more preferable, Furthermore, it is preferable to contain 6-12 mass%.

本発明の皮膚洗浄剤組成物において、成分(A)及び(B)の合計含有量は、より弾力性のある泡を得る観点から、全組成中に2〜40質量%であるのが好ましく、5〜30質量%がより好ましく、更に10〜30質量%であるのが好ましい。   In the skin cleanser composition of the present invention, the total content of components (A) and (B) is preferably 2 to 40% by mass in the total composition from the viewpoint of obtaining more elastic foam, 5-30 mass% is more preferable, and it is further preferable that it is 10-30 mass%.

また、本発明の皮膚洗浄剤組成物において、成分(A)及び(B)を混合することにより、成分(B)の溶解性が高まり、成分(A)の作る泡膜に成分(B)の配向性が高めることができると考えられる。この結果、きめの細かい泡質を得ることができる。特に、成分(A)及び(B)の酸としての質量割合は、泡の弾力性を向上しつっぱり感を抑制する点から、(A)/(B)=0.3〜5が好ましく、0.5〜2であるのがより好ましく、0.5〜1.5であるのが更に好ましい。
さらに、成分(A)及び成分(B)において、一般式(2)中、R2の炭素数が15〜21のアルキル基である脂肪酸(成分(B−1))の酸としての質量割合は、泡の弾力性を向上しつつつっぱり感を抑制する点から、(A)/(B−1)=0.2〜5が好ましく、0.3〜3.5がより好ましく、0.3〜2が更に好ましく、0.4〜2がより更に好ましい。
Moreover, in the skin cleansing composition of the present invention, by mixing the components (A) and (B), the solubility of the component (B) is increased, and the component (B) is added to the foam film formed by the component (A). It is considered that the orientation can be improved. As a result, a fine foam quality can be obtained. In particular, the mass ratio of the components (A) and (B) as the acid is preferably (A) / (B) = 0.3 to 5 from the viewpoint of improving the elasticity of the foam and suppressing the stickiness. More preferably, it is 0.5-2, and it is still more preferable that it is 0.5-1.5.
Furthermore, in the component (A) and the component (B), in the general formula (2), the mass ratio as the acid of the fatty acid (component (B-1)) in which R 2 is an alkyl group having 15 to 21 carbon atoms is (A) / (B-1) = 0.2-5 is preferable, 0.3-3.5 is more preferable, and 0.3-3.5 from the point which improves the elasticity of a bubble and suppresses a twitching feeling. 2 is more preferable, and 0.4 to 2 is even more preferable.

本発明で用いる成分(C)のカチオンポリマーとしては、例えば、カチオン化セルロース、カチオン化澱粉、カチオン化グアーガム、カチオン化タラガム、カチオン化ローカストビーンガム、カチオン化フェヌグリークガム、カチオン化キサンタンガム、ジアリルジアルキル四級アンモニウム塩の重合体、ジアリルジアルキル四級アンモニウム塩/アクリルアミド共重合物、ジアリルジアルキル四級アンモニウム塩/アクリルアミド/アクリル酸共重合物、ビニルイミダゾリウムトリクロライド/ビニルピロリドン共重合体、ヒドロキシエチルセルロース/ジメチルジアリルアンモニウムクロライド共重合体、ビニルピロリドン/四級化ジメチルアミノエチルメタクリレート共重合体、ポリビニルピロリドン/アルキルアミノアクリレート共重合体、ポリビニルピロリドン/アルキルアミノアクリレート/ビニルカプロラクタム共重合体、ビニルピロリドン/メタクリルアミドプロピル塩化トリメチルアンモニウム共重合体、アルキルアクリルアミド/アクリレート/アルキルアミノアルキルアクリルアミド/ポリエチレングリコールメタクリレート共重合体、アジピン酸/ジメチルアミノヒドロキシプロピルエチレントリアミン共重合体(米国サンドス社,カルタレチン)、特開昭53-139734号公報、特開昭60-36407号公報に記載されているカチオン性ポリマー等が挙げられる。
これらのうち、弾力性のある泡を得る観点から、ジアリルジアルキル四級アンモニウム塩/アクリルアミド共重合物、ジアリルジアルキル四級アンモニウム塩/アクリルアミド/アクリル酸共重合物、カチオン化グアーガム、カチオン化セルロースから選ばれる1種又は2種以上が好ましい。
Examples of the cationic polymer of component (C) used in the present invention include, for example, cationized cellulose, cationized starch, cationized guar gum, cationized cod gum, cationized locust bean gum, cationized fenugreek gum, cationized xanthan gum, diallyldialkyl quaternary. Polymer of quaternary ammonium salt, diallyldialkyl quaternary ammonium salt / acrylamide copolymer, diallyldialkyl quaternary ammonium salt / acrylamide / acrylic acid copolymer, vinylimidazolium trichloride / vinyl pyrrolidone copolymer, hydroxyethyl cellulose / dimethyl Diallylammonium chloride copolymer, vinylpyrrolidone / quaternized dimethylaminoethyl methacrylate copolymer, polyvinylpyrrolidone / alkylaminoacrylate copolymer Polymer, polyvinylpyrrolidone / alkylaminoacrylate / vinylcaprolactam copolymer, vinylpyrrolidone / methacrylamideamidopropyltrimethylammonium chloride copolymer, alkylacrylamide / acrylate / alkylaminoalkylacrylamide / polyethylene glycol methacrylate copolymer, adipic acid / dimethylamino Examples thereof include hydroxypropylethylenetriamine copolymer (Sandos Corp., Cartaletin), and cationic polymers described in JP-A-53-139734 and JP-A-60-36407.
Of these, from the viewpoint of obtaining elastic foam, diallyldialkyl quaternary ammonium salt / acrylamide copolymer, diallyldialkyl quaternary ammonium salt / acrylamide / acrylic acid copolymer, cationized guar gum, and cationized cellulose are selected. One type or two or more types are preferred.

成分(C)は、1種以上を用いることができ、より弾力性のある泡を得る観点から、全組成中に0.1質量%以上含有し、好ましくは0.5質量%以上含有し、好ましくは5質量%以下含有し、より好ましくは2質量%以下含有する。また、成分(C)の含有量は、全組成中に0.1〜5質量%であることが好ましく、更に0.5〜2質量%であることが好ましい。   Component (C) can be used in one or more kinds, and from the viewpoint of obtaining more elastic foam, it is contained in an amount of 0.1% by mass or more, preferably 0.5% by mass or more, Preferably it contains 5 mass% or less, More preferably, it contains 2 mass% or less. Moreover, it is preferable that content of a component (C) is 0.1-5 mass% in the whole composition, and it is further preferable that it is 0.5-2 mass%.

本発明で用いる成分(D)の塩基としては、例えば、水酸化ナトリウム、水酸化カリウム等のアルカリ金属の水酸化物;アンモニア;トリエタノールアミン等の有機アミン化合物;アルギニン等の塩基性アミノ酸などが挙げられる。これらの中で、安定性の観点からアルカリ金属の水酸化物が好ましく、液性の調整の点から、水酸化カリウムが好ましい。   Examples of the base of component (D) used in the present invention include alkali metal hydroxides such as sodium hydroxide and potassium hydroxide; ammonia; organic amine compounds such as triethanolamine; and basic amino acids such as arginine. Can be mentioned. Among these, alkali metal hydroxides are preferable from the viewpoint of stability, and potassium hydroxide is preferable from the viewpoint of liquidity adjustment.

本発明において、成分(A)及び(B)は、少なくとも一部が成分(D)と塩で存在する。
成分(D)は、成分(A)及び(B)に対するモル比(成分(D)/(成分(A)+成分(B))が、0.9〜1.1であって、好ましくは0.95〜1.05となるように含有される。このように用いることにより、さらに弾力性のある泡を得ることができる。
In the present invention, components (A) and (B) are at least partially present as component (D) and a salt.
Component (D) has a molar ratio (component (D) / (component (A) + component (B)) to components (A) and (B) of 0.9 to 1.1, preferably 0. It is contained so that it may become 0.95-1.05.By using in this way, a more elastic foam can be obtained.

本発明の皮膚洗浄剤組成物は、更に溶媒として成分(E)水を含有することができる。水は、全組成中に10質量%以上含有するのが好ましく、15質量%以上が好ましく、30質量%以上含有するのがより好ましく、96質量%以下が好ましく、90質量%以下がより好ましく、87質量%以下が更に好ましく、85質量%以下がより更に好ましい。また、水は、全組成中に、好ましくは10〜96質量%、より好ましくは15〜90質量%、さらに好ましくは30〜87質量%含有することができ、洗浄剤組成物を構成する前記成分及びその他成分の残部となる。   The skin cleansing composition of the present invention can further contain component (E) water as a solvent. Water is preferably contained in the total composition in an amount of 10% by mass or more, preferably 15% by mass or more, more preferably 30% by mass or more, preferably 96% by mass or less, more preferably 90% by mass or less, 87 mass% or less is still more preferable, and 85 mass% or less is still more preferable. Further, water can be contained in the total composition, preferably 10 to 96% by mass, more preferably 15 to 90% by mass, and still more preferably 30 to 87% by mass, and the component constituting the cleaning composition. And the balance of other components.

本発明の皮膚洗浄剤組成物は、成分(A)〜(E)を含むことにより、泡のキメが細かくでき、泡の弾力性を向上させることができるため、洗浄時、肌を傷つけにくくなめらかな感触と高い洗浄実感を高めることが可能となり、つっぱり感を抑制することができる。   Since the skin cleanser composition of the present invention contains components (A) to (E), the texture of the foam can be made fine and the elasticity of the foam can be improved, so that the skin is not easily damaged during washing. It is possible to enhance the feel and high cleaning feeling, and to suppress the feeling of tension.

本発明の皮膚洗浄剤組成物は、さらに、(F)ポリオールを含有することができ、洗い上がりの肌がしっとりしてつっぱらない感触をより向上させることができる。
かかるポリオールとしては、例えば、ソルビトール、グリセリン、ブチレングリコール、プロピレングリコール、ジプロピレングリコール、エリスリトール、マンニトール、キシリトール等が挙げられる。これらのうち、洗い上がりの肌がよりしっとりしてつっぱらないという肌感触と泡の弾力性の観点からグリセリン、ソルビトールが好ましい。
The skin cleansing composition of the present invention can further contain (F) a polyol, and can further improve the feeling that the washed-out skin is moist and not sticking.
Examples of such polyols include sorbitol, glycerin, butylene glycol, propylene glycol, dipropylene glycol, erythritol, mannitol, xylitol and the like. Of these, glycerin and sorbitol are preferred from the viewpoint of the skin feel that the washed-up skin is moist and not sticky and the elasticity of the foam.

成分(F)のポリオールは、1種以上を用いることができ、洗い上がりの肌感触の点から、全組成中に1質量%以上含有することが好ましく、より好ましくは5質量%以上含有し、40質量%以下含有することが好ましく、より好ましくは30質量%以下含有する。また、成分(F)は全組成中に、1〜40質量%含有するのが好ましく、5〜30質量%含有するのがより好ましい。   As the component (F) polyol, one or more types can be used, and from the viewpoint of the skin feel after washing, the total composition preferably contains 1% by mass or more, more preferably 5% by mass or more, The content is preferably 40% by mass or less, and more preferably 30% by mass or less. Moreover, it is preferable to contain 1-40 mass% in a whole composition, and, as for a component (F), it is more preferable to contain 5-30 mass%.

本発明の皮膚洗浄剤組成物は、更に、通常の洗浄剤に用いられる成分、例えば、成分(A)及び(B)以外の界面活性剤、保湿剤、油性成分、殺菌剤、抗炎症剤、防腐剤、キレート剤、増粘剤、成分(D)以外の塩類、パール化剤、スクラブ剤、香料、冷感剤、色素、紫外線吸収剤、酸化防止剤、植物エキス等を含有することができる。   The skin cleanser composition of the present invention further comprises components used in ordinary cleansing agents, for example, surfactants other than components (A) and (B), moisturizers, oily components, bactericides, anti-inflammatory agents, Preservatives, chelating agents, thickeners, salts other than component (D), pearling agents, scrub agents, fragrances, cooling agents, dyes, ultraviolet absorbers, antioxidants, plant extracts, etc. .

本発明の皮膚洗浄剤組成物は、通常の方法により、配合成分を混合することにより製造される。得られる洗浄剤組成物は、液状又は固形状いずれでも良いが、液状である場合には、25℃において、B型粘度計(東京計器社製)で測定したときの粘度が200〜80000mPa・s であるのが好ましく、配合成分を適宜選択することにより調整することができる。
また、pHは、3〜12であることが好ましく、5〜10.5がより好ましく、5〜7であるのが更に好ましい。なお、pHの測定は、25℃において、各洗浄剤組成物をイオン交換水で20倍に希釈して行った値である。
The skin cleansing composition of the present invention is produced by mixing the compounding ingredients by a usual method. The obtained detergent composition may be either liquid or solid, but when it is liquid, the viscosity when measured with a B-type viscometer (manufactured by Tokyo Keiki Co., Ltd.) at 25 ° C. is 200 to 80,000 mPa · s. It is preferable that it can be adjusted by appropriately selecting the blending components.
Moreover, it is preferable that pH is 3-12, 5-10.5 is more preferable, and it is still more preferable that it is 5-7. In addition, the measurement of pH is a value obtained by diluting each cleaning composition 20 times with ion-exchanged water at 25 ° C.

本発明の皮膚洗浄剤組成物は、例えば、洗顔料、ボディーソープ、ハンドソープ等として好適であり、洗顔料、ボディーソープが好ましい。
本発明の皮膚洗浄剤組成物を用いて皮膚を洗浄する方法は、例えば、以下のとおりである。すなわち、本発明の皮膚洗浄剤組成物を身体、つまり顔、手足、胴体などの身体皮膚部に適量を適用し、泡立てて洗浄した後、シャワー等の温水を利用してすすぐ方法である。また、樹脂製のタオル、樹脂製のスポンジ、ブラシ等の洗浄補助具に適量を適用し、泡立てて使用することで、より効果的に洗浄することもできる。
上述した実施形態に関し、本発明は、更に以下の組成物、方法、使用を開示する。
The skin cleansing composition of the present invention is suitable as, for example, a facial cleanser, body soap, hand soap, etc., and a facial cleanser and body soap are preferred.
The method for washing the skin using the skin cleansing composition of the present invention is, for example, as follows. That is, the skin cleansing composition of the present invention is a method of applying an appropriate amount to the body, that is, the body skin such as the face, limbs, and torso, washing with foaming, and then rinsing using warm water such as a shower. Moreover, it can also wash | clean more effectively by applying a suitable amount to washing aids, such as a resin towel, resin sponge, and a brush, and using it lathering.
The present invention further discloses the following compositions, methods and uses with respect to the above-described embodiments.

<1>次の成分(A)、(B)、(C)、(D)及び(E):
(A)一般式(1)
<1> The following components (A), (B), (C), (D) and (E):
(A) General formula (1)

Figure 2013139439
Figure 2013139439

(式中、R1は炭素数4〜22のアルキル基を示し、nは0〜20の数を示す)
で表されるアルキルエーテルカルボン酸であって、R1の平均炭素数が10.8〜12.8であり、n=0の成分を4.3〜30質量%含み、n=1の成分とn=2の成分の合計含有量が20質量%以上40質量%未満であるアルキルエーテルカルボン酸 1〜20質量%、
(B)一般式(2)
(In the formula, R 1 represents an alkyl group having 4 to 22 carbon atoms, and n represents a number of 0 to 20).
Wherein R 1 has an average carbon number of 10.8 to 12.8, 4.3 to 30% by mass of n = 0, and n = 1 1-20% by mass of an alkyl ether carboxylic acid having a total content of n = 2 components of 20% by mass or more and less than 40% by mass,
(B) General formula (2)

Figure 2013139439
Figure 2013139439

(式中、R2は炭素数9〜21の直鎖又は分岐鎖のアルキル基又はアルケニル基を示す)
で表される脂肪酸 1〜20質量%、
(C)カチオンポリマー 0.1〜5質量%、
(D)塩基、
(E)水
を含有し、成分(A)及び(B)は、少なくとも一部が成分(D)と塩で存在し、成分(D)は、成分(A)及び(B)に対するモル比(成分(D)/(成分(A)+成分(B))が0.9〜1.1である皮膚洗浄剤組成物。
(Wherein R 2 represents a linear or branched alkyl or alkenyl group having 9 to 21 carbon atoms)
1 to 20% by mass of a fatty acid represented by
(C) Cationic polymer 0.1-5% by mass,
(D) a base,
(E) It contains water, and components (A) and (B) are at least partially present as component (D) and salt, and component (D) is a molar ratio of components (A) and (B) ( Skin cleanser composition whose component (D) / (component (A) + component (B)) is 0.9-1.1.

<2>成分(A)において、一般式(1)中、R1は炭素数4〜22のアルキル基であり、炭素数6〜20のアルキル基、更に炭素数8〜18のアルキル基、更には炭素数8〜16のアルキル基が好ましく、炭素数10〜16のアルキル基がより好ましく、また、R1のアルキル鎖は、直鎖又は分岐鎖のいずれでも良いが、直鎖アルキル基が好ましい前記<1>記載の皮膚洗浄剤組成物。
<3>成分(A)において、一般式(1)中、R1の平均炭素数が、10.8〜12.8であり、好ましくは10.8〜12.5、より好ましくは12.1〜12.4である前記<1>又は<2>記載の皮膚洗浄剤組成物。
<4>成分(A)において、一般式(1)中、R1は2種以上のアルキル基を含み、一番含有量の多いアルキル鎖長を有する成分が55質量%以上97質量%未満であるのが好ましく、60〜95質量%がより好ましく、70〜95質量%が更に好ましい前記<1>〜<3>のいずれか1記載の皮膚洗浄剤組成物。
<2> In the component (A), in the general formula (1), R 1 is an alkyl group having 4 to 22 carbon atoms, an alkyl group having 6 to 20 carbon atoms, an alkyl group having 8 to 18 carbon atoms, and Is preferably an alkyl group having 8 to 16 carbon atoms, more preferably an alkyl group having 10 to 16 carbon atoms, and the alkyl chain of R 1 may be either linear or branched, but is preferably a linear alkyl group. The skin cleansing composition according to <1>.
<3> In the component (A), in the general formula (1), the average carbon number of R 1 is 10.8 to 12.8, preferably 10.8 to 12.5, more preferably 12.1. The skin cleansing composition according to <1> or <2> above, which is ˜12.4.
<4> In component (A), in general formula (1), R 1 contains two or more alkyl groups, and the component having the largest alkyl chain length is 55% by mass or more and less than 97% by mass The skin cleanser composition according to any one of <1> to <3>, preferably 60 to 95% by mass, more preferably 70 to 95% by mass.

<5>成分(A)において、一般式(1)中、nの平均値(平均付加モル数)が1.5〜10が好ましく、2.5〜4.5がより好ましく、2.5〜3.4が更に好ましく、2.8〜3.4がより更に好ましく、2.8〜3.1がより更に好ましい前記<1>〜<4>のいずれか1記載の皮膚洗浄剤組成物。
<6>成分(A)において、一般式(1)中、n=0の成分を4.3〜30質量%含み、4.9〜27質量%が好ましく、9.6〜27質量%がより好ましく、9.9〜16質量%が更に好ましく、9.9〜15質量%含むのがより更に好ましい前記<1>〜<5>のいずれか1記載の皮膚洗浄剤組成物。
<5> In the component (A), in the general formula (1), the average value (average number of added moles) of n is preferably 1.5 to 10, more preferably 2.5 to 4.5, and 2.5 to 3.4 is still more preferable, 2.8-3.4 is still more preferable, 2.8-3.1 is still more preferable, The skin cleaning composition in any one of said <1>-<4>.
In <6> component (A), in general formula (1), the component of n = 0 is 4.3-30 mass%, 4.9-27 mass% is preferable, and 9.6-27 mass% is more. Preferably, 9.9-16 mass% is still more preferable, It is still more preferable that it contains 9.9-15 mass%, The skin cleaning composition in any one of said <1>-<5>.

<7>成分(A)において、一般式(1)中、n=1の成分とn=2の成分の合計含有量が、20〜37質量%が好ましく、27〜36.6質量%がより好ましく、35〜36.1質量%が更に好ましい前記<1>〜<6>のいずれか1記載の皮膚洗浄剤組成物。
<8>成分(A)において、一般式(1)中、R1が炭素数6〜20のアルキル基であり、R1の平均炭素数は10.8〜12.8であり、また、一番含有量の多いアルキル鎖長を有する成分が55質量%以上97質量%未満であり、更に、nは0〜20の数を示し、nの平均値が2.5〜4.5であり、n=0の成分を9.6〜27質量%含み、n=1の成分とn=2の成分の合計含有量が27〜36.5質量%であることが好ましい前記<1>〜<7>のいずれか1記載の皮膚洗浄剤組成物。
<7> In the component (A), in the general formula (1), the total content of the n = 1 component and the n = 2 component is preferably 20 to 37% by mass, and more preferably 27 to 36.6% by mass. The skin cleanser composition according to any one of <1> to <6>, preferably 35 to 36.1% by mass.
<8> In the component (A), in the general formula (1), R 1 is an alkyl group having 6 to 20 carbon atoms, and the average carbon number of R 1 is 10.8 to 12.8. The component having an alkyl chain length with a large number content is 55% by mass or more and less than 97% by mass, n represents a number of 0 to 20, and the average value of n is 2.5 to 4.5, <1> to <7, wherein the content of n = 0 is 9.6 to 27% by mass, and the total content of the component n = 1 and the component n = 2 is preferably 27 to 36.5% by mass. > The skin cleanser composition of any one of>.

<9>成分(A)において、一般式(1)中、R1が炭素数8〜18のアルキル基であり、R1の平均炭素数は10.8〜12.8であり、また、一番含有量の多いアルキル鎖長を有する成分が55質量%以上97質量%未満であり、更に、nは0〜20の数を示し、nの平均値が2.5〜3.4であり、n=0の成分を9.6〜27質量%含み、n=1の成分とn=2の成分の合計含有量が27〜36.5質量%であることが好ましい前記<1>〜<8>のいずれか1記載の皮膚洗浄剤組成物。
<10>成分(A)において、一般式(1)中、R1が炭素数8〜16のアルキル基であり、R1の平均炭素数は10.8〜12.5であり、また、一番含有量の多いアルキル鎖長を有する成分が60〜95質量%であり、更に、nは0〜20の数を示し、nの平均値が2.8〜3.4であり、n=0の成分を9.6〜27質量%含み、n=1の成分とn=2の成分の合計含有量が27〜36.5質量%であることが好ましい前記<1>〜<9>のいずれか1記載の皮膚洗浄剤組成物。
<9> In the component (A), in the formula (1), R 1 is an alkyl group having 8 to 18 carbon atoms, the average number of carbon atoms in R 1 is 10.8 to 12.8, also one The component having an alkyl chain length with a large number content is 55% by mass or more and less than 97% by mass, and n represents a number of 0 to 20, and the average value of n is 2.5 to 3.4. <1> to <8, wherein the content of n = 0 is 9.6 to 27% by mass, and the total content of n = 1 and n = 2 is preferably 27 to 36.5% by mass. > The skin cleanser composition of any one of>.
<10> In the component (A), in the general formula (1), R 1 is an alkyl group having 8 to 16 carbon atoms, and the average carbon number of R 1 is 10.8 to 12.5. The component having an alkyl chain length with a large number content is 60 to 95% by mass, n represents a number of 0 to 20, the average value of n is 2.8 to 3.4, and n = 0 Any of the above <1> to <9>, wherein the total content of the component of n = 1 and the component of n = 2 is preferably 27 to 36.5% by mass 2. A skin cleanser composition according to claim 1.

<11>成分(A)において、一般式(1)中、R1は炭素数10〜16のアルキル基であり、R1の平均炭素数は12.1〜12.4であり、また、一番含有量の多いアルキル鎖長を有する成分が60〜95質量%であり、更に、nは0〜20の数を示し、nの平均値は2.8〜3.1であり、n=0の成分を9.9〜15質量%含み、n=1の成分とn=2の成分の合計含有量が35〜36.1質量%であることが好ましい前記<1>〜<10>のいずれか1記載の皮膚洗浄剤組成物。
<12>成分(A)のアルキルエーテルカルボン酸は、全組成中に1質量%以上含有することが好ましく、5質量%以上がより好ましく、6質量%以上含有することがさらに好ましく、全組成中に20質量%以下が好ましく、15質量%以下がより好ましく、12質量%以下が更に好ましく、全組成中に1〜20質量%含有するのが好ましく、2〜15質量%がより好ましく、4〜12質量%含有されるのが更に好ましい前記<1>〜<11>のいずれか1記載の皮膚洗浄剤組成物。
<11> In the component (A), in the general formula (1), R 1 is an alkyl group having 10 to 16 carbon atoms, and the average carbon number of R 1 is 12.1 to 12.4. The component having an alkyl chain length with a large number content is 60 to 95% by mass, n represents a number of 0 to 20, the average value of n is 2.8 to 3.1, and n = 0 Any one of the above items <1> to <10>, wherein 9.9 to 15% by mass of the component is included, and the total content of the n = 1 component and the n = 2 component is preferably 35 to 36.1% by mass 2. A skin cleanser composition according to claim 1.
<12> The alkyl ether carboxylic acid of component (A) is preferably contained in an amount of 1% by mass or more, more preferably 5% by mass or more, and further preferably 6% by mass or more in the entire composition. 20 mass% or less is preferable, 15 mass% or less is more preferable, 12 mass% or less is further more preferable, 1-20 mass% is contained in the whole composition, 2-15 mass% is more preferable, 4- The skin cleanser composition according to any one of the above items <1> to <11>, more preferably 12% by mass.

<13>成分(A)において、一般式(1)中、(n=0成分の質量):(n=1成分の質量):(n=2成分の質量):(n=3成分の質量):(n=4成分の質量)=1:0.99〜3.50:0.89〜3.00:0.76〜3.00:0.63〜1.6となることが好ましい前記<1>〜<12>のいずれか1記載の皮膚洗浄剤組成物。
<14>成分(A)において、一般式(1)中、n=0の成分を9.6質量%以上12質量%未満含み、(n=0成分の質量):(n=1成分の質量):(n=2成分の質量):(n=3成分の質量):(n=4成分の質量)=1:1.53〜1.87:1.59〜2.25:1.33〜2.16:1.14〜1.52となるか、又は、n=0の成分を12質量%以上17質量%以下含み、(n=0成分の質量):(n=1成分の質量):(n=2成分の質量):(n=3成分の質量):(n=4成分の質量)=1:0.99〜1.34:0.89〜1.40:0.76〜1.23:0.63〜0.99となることが好ましい前記<1>〜<13>のいずれか1記載の皮膚洗浄剤組成物。
In <13> component (A), in general formula (1), (mass of n = 0 component) :( mass of n = 1 component) :( mass of n = 2 component) :( mass of n = 3 component) ): (Mass of n = 4 components) = 1: 0.99 to 3.50: 0.89 to 3.00: 0.76 to 3.00: 0.63 to 1.6 The skin cleanser composition according to any one of <1> to <12>.
<14> In the component (A), in the general formula (1), a component of n = 0 is contained in an amount of 9.6% by mass to less than 12% by mass, and (mass of n = 0 component): (mass of n = 1 component) ): (Mass of n = 2 components): (mass of n = 3 components): (mass of n = 4 components) = 1: 1.53-1.87: 1.59-2.25: 1.33 To 2.16: 1.14 to 1.52, or a component of n = 0 is contained in an amount of 12% by mass to 17% by mass, (mass of n = 0 component): (mass of n = 1 component) ): (Mass of n = 2 components): (mass of n = 3 components): (mass of n = 4 components) = 1: 0.99-1.34: 0.89-1.40: 0.76 ~ 1.23: The skin cleanser composition according to any one of <1> to <13>, which is preferably 0.63 to 0.99.

<15>成分(A)において、一般式(1)中、n=0の成分を9.9〜11.5質量%含み、(n=0成分の質量):(n=1成分の質量):(n=2成分の質量):(n=3成分の質量):(n=4成分の質量)=1:1.58〜1.84:1.72〜2.17:1.49〜2.00:1.14〜1.52となるか、又は、一般式(1)中、n=0の成分を13〜17質量%含み、(n=0成分の質量):(n=1成分の質量):(n=2成分の質量):(n=3成分の質量):(n=4成分の質量)=1:1.00〜1.31:0.93〜1.34:0.79〜1.18:0.63〜0.99となることが好ましい前記<1>〜<14>のいずれか1記載の皮膚洗浄剤組成物。
<16>成分(A)において、一般式(1)中、R1は炭素数4〜22のアルキル基であり、R1の平均炭素数は10.8〜12.8であり、また、一番含有量の多いアルキル鎖長を有する成分が55質量%以上97質量%未満であり、更に、nは0〜20の数を示し、平均値は、1.5〜10であり、n=0の成分を4.9〜27質量%含み、n=1の成分とn=2の成分の合計含有量が20〜37質量%であることが好ましい前記<1>〜<15>のいずれか1記載の皮膚洗浄剤組成物。
<15> In the component (A), in the general formula (1), the component of n = 0 is included in the range of 9.9 to 11.5% by mass, (the mass of the n = 0 component): (the mass of the n = 1 component) : (Mass of n = 2 components): (mass of n = 3 components): (mass of n = 4 components) = 1: 1.58-1.84: 1.72-2.17: 1.49- 2.00: 1.14 to 1.52 or, in the general formula (1), 13 to 17% by mass of n = 0 component (n = 0 component mass): (n = 1 Component mass): (n = 2 component mass): (n = 3 component mass): (n = 4 component mass) = 1: 1.00 to 1.31: 0.93 to 1.34: The skin cleansing composition according to any one of <1> to <14>, preferably 0.79 to 1.18: 0.63 to 0.99.
<16> In the component (A), in the general formula (1), R 1 is an alkyl group having 4 to 22 carbon atoms, and the average carbon number of R 1 is 10.8 to 12.8. The component having an alkyl chain length with a large number content is 55% by mass or more and less than 97% by mass, n represents a number of 0 to 20, an average value is 1.5 to 10, and n = 0 Any one of the above items <1> to <15>, wherein the total content of the components of 4.9 to 27% by mass and the component of n = 1 and the component of n = 2 is preferably 20 to 37% by mass. The skin cleansing composition as described.

<17>成分(B)の脂肪酸において、一般式(2)中、R2は炭素数9〜21のアルキル基又はアルケニル基が好ましく、直鎖又は分岐鎖のいずれでも良く、炭素数11〜21のアルキル基がより好ましく、更に炭素数13〜17のアルキル基が好ましく、ミリスチン酸、パルミチン酸、ステアリン酸又はべヘン酸が更に好ましい前記<1>〜<16>のいずれか1記載の皮膚洗浄剤組成物。
<18>成分(B)の脂肪酸は、1種又は2種以上を用いることができ、全組成中に1質量%以上含有することが好ましく、5質量%以上がより好ましく、6質量%以上が更に好ましく、20質量%以下が好ましく、15質量%以下がより好ましく、12質量%が更に好ましく、全組成中に1〜20質量%含有するのが好ましく、5〜15質量%がより好ましく、6〜12質量%含有するのが更に好ましい前記<1>〜<17>のいずれか1記載の皮膚洗浄剤組成物。
<17> In the fatty acid of component (B), in general formula (2), R 2 is preferably an alkyl group or alkenyl group having 9 to 21 carbon atoms, and may be either a straight chain or branched chain, and has 11 to 21 carbon atoms. Skin alkyl according to any one of <1> to <16>, more preferably an alkyl group having 13 to 17 carbon atoms, more preferably myristic acid, palmitic acid, stearic acid or behenic acid. Agent composition.
The fatty acid of <18> component (B) can use 1 type (s) or 2 or more types, It is preferable to contain 1 mass% or more in the whole composition, 5 mass% or more is more preferable, 6 mass% or more is preferable. More preferably, 20% by mass or less is preferable, 15% by mass or less is more preferable, 12% by mass is further preferable, 1 to 20% by mass is preferably contained in the total composition, 5 to 15% by mass is more preferable, and 6% by mass. The skin cleansing composition according to any one of the above <1> to <17>, which is further preferably contained in an amount of ˜12% by mass.

<19>成分(A)及び(B)の合計含有量は、全組成中に2〜40質量%であるのが好ましく、5〜30質量%がより好ましく、10〜30質量%であるのが更に好ましい前記<1>〜<18>のいずれか1記載の皮膚洗浄剤組成物。
<20>成分(B)が、一般式(2)中、R2の炭素数が15〜21の脂肪酸を40〜100質量%含有することが好ましく、50〜80質量%含有することがさらに好ましい前記<1>〜<19>のいずれか1記載の皮膚洗浄剤組成物。
<21>成分(A)及び(B)の酸としての質量割合が、(A)/(B)=0.3〜5であることが好ましく、0.5〜2がより好ましく、0.5〜1.5がさらに好ましい前記<1>〜<20>のいずれか1記載の皮膚洗浄剤組成物。
<22>成分(A)及び成分(B)において、一般式(2)中、R2の炭素数が15〜21のアルキル基である脂肪酸(成分(B−1))の酸としての質量割合が、(A)/(B−1)=0.2〜5が好ましく、0.3〜3.5がより好ましく、0.3〜2が更に好ましく、0.4〜2がより更に好ましい前記<1>〜<21>のいずれか1記載の皮膚洗浄剤組成物。
<19> The total content of components (A) and (B) is preferably 2 to 40% by mass, more preferably 5 to 30% by mass, and 10 to 30% by mass in the total composition. The skin cleansing composition according to any one of <1> to <18>, which is more preferable.
<20> The component (B) preferably contains 40 to 100% by mass, more preferably 50 to 80% by mass, of the fatty acid having 15 to 21 carbon atoms in R 2 in the general formula (2). The skin cleansing composition according to any one of <1> to <19>.
It is preferable that the mass ratio as an acid of <21> component (A) and (B) is (A) / (B) = 0.3-5, 0.5-2 are more preferable, 0.5 The skin cleanser composition according to any one of <1> to <20>, wherein -1.5 is more preferable.
<22> In the component (A) and the component (B), in the general formula (2), the mass ratio of the fatty acid (component (B-1)) in which R 2 is an alkyl group having 15 to 21 carbon atoms as an acid. Is preferably (A) / (B-1) = 0.2-5, more preferably 0.3-3.5, still more preferably 0.3-2, and still more preferably 0.4-2. The skin cleanser composition according to any one of <1> to <21>.

<23>成分(C)が、好ましくは、カチオン化セルロース、カチオン化澱粉、カチオン化グアーガム、カチオン化タラガム、カチオン化ローカストビーンガム、カチオン化フェヌグリークガム、カチオン化キサンタンガム、ジアリルジアルキル四級アンモニウム塩の重合体、ジアリルジアルキル四級アンモニウム塩/アクリルアミド共重合物、ジアリルジアルキル四級アンモニウム塩/アクリルアミド/アクリル酸共重合物、ビニルイミダゾリウムトリクロライド/ビニルピロリドン共重合体、ヒドロキシエチルセルロース/ジメチルジアリルアンモニウムクロライド共重合体、ビニルピロリドン/四級化ジメチルアミノエチルメタクリレート共重合体、ポリビニルピロリドン/アルキルアミノアクリレート共重合体、ポリビニルピロリドン/アルキルアミノアクリレート/ビニルカプロラクタム共重合体、ビニルピロリドン/メタクリルアミドプロピル塩化トリメチルアンモニウム共重合体、アルキルアクリルアミド/アクリレート/アルキルアミノアルキルアクリルアミド/ポリエチレングリコールメタクリレート共重合体、アジピン酸/ジメチルアミノヒドロキシプロピルエチレントリアミン共重合体(米国サンドス社,カルタレチン)、特開昭53-139734号公報、特開昭60-36407号公報に記載されているカチオン性ポリマーであり、より好ましくは、ジアリルジアルキル四級アンモニウム塩/アクリルアミド共重合物、ジアリルジアルキル四級アンモニウム塩/アクリルアミド/アクリル酸共重合物、カチオン化グアーガム及びカチオン化セルロースから選ばれる1種又は2種以上である前記<1>〜<22>のいずれか1記載の皮膚洗浄剤組成物。
<24>成分(C)は、1種以上を用いることができ、全組成中に0.1質量%以上含有することが好ましく、0.5質量%以上がより好ましく、5質量%以下含有することが好ましく、2質量%以下がより好ましく、また、全組成中に0.1〜5質量%含有することが好ましく、0.5〜2質量%であることがより好ましい前記<1>〜<23>のいずれか1記載の皮膚洗浄剤組成物。
<23> Component (C) is preferably cationized cellulose, cationized starch, cationized guar gum, cationized cod gum, cationized locust bean gum, cationized fenugreek gum, cationized xanthan gum, diallyldialkyl quaternary ammonium salt Polymer, diallyldialkyl quaternary ammonium salt / acrylamide copolymer, diallyldialkyl quaternary ammonium salt / acrylamide / acrylic acid copolymer, vinylimidazolium trichloride / vinylpyrrolidone copolymer, hydroxyethylcellulose / dimethyldiallylammonium chloride Polymer, vinylpyrrolidone / quaternized dimethylaminoethyl methacrylate copolymer, polyvinylpyrrolidone / alkylaminoacrylate copolymer, polyvinylpyrrolide / Alkylamino acrylate / vinyl caprolactam copolymer, vinyl pyrrolidone / methacrylamidopropyl trimethylammonium chloride copolymer, alkylacrylamide / acrylate / alkylaminoalkylacrylamide / polyethylene glycol methacrylate copolymer, adipic acid / dimethylaminohydroxypropylethylenetriamine Copolymer (Sandos Corp., Cartaletin), a cationic polymer described in JP-A-53-139734, JP-A-60-36407, more preferably a diallyldialkyl quaternary ammonium salt / One or more selected from acrylamide copolymer, diallyldialkyl quaternary ammonium salt / acrylamide / acrylic acid copolymer, cationized guar gum and cationized cellulose The skin cleanser composition according to any one of <1> to <22> above.
<24> Component (C) can use 1 or more types, It is preferable to contain 0.1 mass% or more in all the compositions, 0.5 mass% or more is more preferable, and 5 mass% or less is contained. The content is preferably 2% by mass or less, more preferably 0.1 to 5% by mass in the total composition, and more preferably 0.5 to 2% by mass. 23> The skin cleansing composition of any one of 23>.

<25>成分(D)の塩基としては、水酸化ナトリウム、水酸化カリウムのアルカリ金属の水酸化物;アンモニア;トリエタノールアミンの有機アミン化合物;アルギニンの塩基性アミノ酸が好ましく、水酸化カリウムがより好ましい前記<1>〜<24>のいずれか1記載の皮膚洗浄剤組成物。
<26>成分(D)は、成分(A)及び(B)に対するモル比(成分(D)/(成分(A)+成分(B))が、0.9〜1.1が好ましく、0.95〜1.05がより好ましい前記<1>〜<25>のいずれか1記載の皮膚洗浄剤組成物。
<27>更に溶媒として成分(E)水を含有し、含有量は、全組成中に10質量%以上が好ましく、15質量%以上がより好ましく、30質量%以上が更に好ましく、96質量%以下が好ましく、90質量%以下がより好ましく、87質量%以下が更に好ましく、85質量%以下より更に好ましく、また、全組成中に10〜96質量%が好ましく、15〜90質量%がより好ましく、30〜87質量%が更に好ましい前記<1>〜<26>のいずれか1記載の皮膚洗浄剤組成物。
<25> The base of component (D) is preferably alkali metal hydroxide of sodium hydroxide or potassium hydroxide; ammonia; organic amine compound of triethanolamine; basic amino acid of arginine, more preferably potassium hydroxide. The skin cleansing composition according to any one of the above <1> to <24>.
<26> Component (D) preferably has a molar ratio (component (D) / (component (A) + component (B)) to components (A) and (B) of 0.9 to 1.1, 0 The skin cleansing composition according to any one of <1> to <25>, more preferably from .95 to 1.05.
<27> Further, component (E) water is contained as a solvent, and the content is preferably 10% by mass or more, more preferably 15% by mass or more, still more preferably 30% by mass or more, and 96% by mass or less in the total composition. Is preferable, 90% by mass or less is more preferable, 87% by mass or less is more preferable, 85% by mass or less is more preferable, 10 to 96% by mass is preferable in the total composition, and 15 to 90% by mass is more preferable. The skin cleanser composition according to any one of <1> to <26>, wherein 30 to 87% by mass is more preferable.

<28>さらに、(F)ポリオールを含有することが好ましい前記<1>〜<27>のいずれか1記載の皮膚洗浄剤組成物。
<29>成分(F)ポリオールとしては、ソルビトール、グリセリン、ブチレングリコール、プロピレングリコール、ジプロピレングリコール、エリスリトール、マンニトール、キシリトールが好ましく、グリセリン、ソルビトールがより好ましい前記<28>記載の皮膚洗浄剤組成物。
<30>成分(F)のポリオールは、1種以上を用いることができ、全組成中に1質量%以上含有することが好ましく、5質量%以上がより好ましく、40質量%以下含有することが好ましく、30質量%以下がより好ましく、また、全組成中に、1〜40質量%含有するのが好ましく、5〜30質量%含有するのがより好ましい前記<28>又は<29>記載の皮膚洗浄剤組成物。
<28> The skin cleanser composition according to any one of <1> to <27>, which preferably further comprises (F) a polyol.
<29> Component (F) As the polyol, sorbitol, glycerin, butylene glycol, propylene glycol, dipropylene glycol, erythritol, mannitol, and xylitol are preferable, and glycerin and sorbitol are more preferable. .
As the polyol of <30> component (F), one or more kinds can be used, and the total composition preferably contains 1% by mass or more, more preferably 5% by mass or more, and 40% by mass or less. Preferably, 30% by mass or less, more preferably 1 to 40% by mass, and more preferably 5 to 30% by mass in the total composition, the skin according to <28> or <29> Cleaning composition.

<31>本発明の皮膚洗浄剤組成物は、通常の方法により、配合成分を混合することにより製造され、得られる洗浄剤組成物は、液状又は固形状いずれでも良いが、液状である場合には、25℃において、B型粘度計(東京計器社製)で測定したときの粘度が200〜80000mPa・s であることが好ましい前記<1>〜<30>のいずれか1記載の皮膚洗浄剤組成物。
<32>本発明の皮膚洗浄剤組成物は、pHは、3〜12であることが好ましく、5〜10.5がより好ましく、5〜7であるのが更に好ましい前記<1>〜<31>のいずれか1記載の皮膚洗浄剤組成物。
<33>本発明の皮膚洗浄剤組成物は、洗顔料、ボディーソープ、ハンドソープとして好適であり、洗顔料、ボディーソープが好ましい前記<1>〜<32>のいずれか1記載の皮膚洗浄剤組成物。
<31> The skin cleanser composition of the present invention is produced by mixing the blending components by a usual method, and the resulting cleanser composition may be either liquid or solid, but is liquid. Preferably has a viscosity of 200 to 80000 mPa · s when measured with a B-type viscometer (manufactured by Tokyo Keiki Co., Ltd.) at 25 ° C. <1> to <30> Composition.
<32> The skin cleansing composition of the present invention preferably has a pH of 3 to 12, more preferably 5 to 10.5, and still more preferably 5 to 7 <1> to <31. > The skin cleanser composition of any one of>.
<33> The skin cleanser composition of the present invention is suitable as a face wash, body soap, and hand soap, and preferably a face cleanser and body soap. <1> to <32> Composition.

<34>前記<1>〜<33>のいずれか1記載の皮膚洗浄剤組成物を、身体皮膚部に適用して洗浄した後、すすぐ皮膚洗浄方法。
<35>肌に適用して泡で洗う洗浄剤製造のための、前記<1>〜<33>のいずれか1記載の皮膚洗浄剤組成物の使用。
<34> A method for rinsing the skin after applying the skin cleanser composition according to any one of <1> to <33> to a body skin part and washing the body.
<35> Use of the skin cleanser composition according to any one of <1> to <33> for manufacturing a cleanser applied to the skin and washed with foam.

(測定方法)
本発明において、アルキルエーテルカルボン酸のアルキル組成、EO付加モル分布及び各成分の比率は、ガスクロマトグラフィー(GC)により、以下の分析方法で測定した。
(Measuring method)
In the present invention, the alkyl composition, EO addition molar distribution, and ratio of each component of the alkyl ether carboxylic acid were measured by gas chromatography (GC) by the following analytical method.

(GC分析条件)
GC機器;アジレントテクノロジー社製、7890A
カラム;アジレントテクノロジー社製、DB−5
(30m、内径0.25mm、膜厚0.25μm)
検出器;FID
キャリア;ヘリウムガス、1mL/min
昇温条件;100℃から325℃まで5℃/minで昇温。その後、35分間325℃を保持。
(GC analysis conditions)
GC equipment; Agilent Technologies, 7890A
Column; manufactured by Agilent Technologies, DB-5
(30m, inner diameter 0.25mm, film thickness 0.25μm)
Detector; FID
Carrier; helium gas, 1mL / min
Temperature rising condition: Temperature raised from 100 ° C. to 325 ° C. at 5 ° C./min. Then, hold 325 ° C. for 35 minutes.

(サンプルの前処理方法)
アルキルエーテルカルボン酸150mgをメタノール50mLで溶解した。また、洗浄剤組成物については、アルキルエーテルカルボン酸として150mgとなるよう採取し、メタノール50mLで溶解した。なお、洗浄剤組成物がポリオキシエチレンアルキルエーテル硫酸塩などの強アニオン性の界面活性剤を含む場合、それらが250mg以下となるように採取した。この溶液1mLを採取して、あらかじめメタノール4mLでコンディショニングを行った固相カートリッジ(Biotage製、Isolute SAX、1g、3mL、500-0100-B)に適用し、10mL丸底試験管に通過液を捕集した。その後、ギ酸4.6gに100mLのメタノールを加えた溶液6mLで溶出し、溶出液についても同じ試験管に捕集した。捕集した溶液は、50℃に加温したブロックヒーターに設置し、窒素ガスを吹き込み、1mL程度まで濃縮した後、さらに室温下で窒素ガスを吹き込み乾燥させた。そこに、ジアゾメタン−エーテル溶液2mLを加え、攪拌しながら室温下で10分間放置し誘導体化を行った。その後、室温下で窒素ガスを吹き込み、500μL以下になるまで濃縮した後、クロロホルムを加えて500μLとし、GC分析に供した。
なお、ジアゾメタン−エーテル溶液は、ジアゾメタン生成装置(宮本理研工業製、GM−50)を用い、以下の手順で調製した。第1と第2の受け器、第2と第3の受け器をシリコンゴム栓およびテフロン(登録商標)チューブで連結する。第2の受け器に、N−メチル−N'−ニトロ−N−ニトロソグアニジン0.8gを採取し、2.5mLのイオン交換水を加えた。第3の受け器に、t−ブチルメチルエーテル10mLを採取した。第1、第2、第3の受け器を氷冷した。続いて第2の受け器に、プラスチックシリンジを備え付け、このシリンジ中に水酸化ナトリウム20gをイオン交換水100mLに溶解させた溶液3mLを入れた。この水酸化ナトリウム水溶液をゆっくりと滴下してジアゾメタンガスを生成させ、第1の受け器側から静かに窒素ガスを吹き込み、第3の受け器のt−ブチルメチルエーテルに溶解させて、ジアゾメタン−エーテル溶液を得た。
上記サンプルの前処理における試薬は以下のものを使用した。
メタノール(関東化学製、高速液体クロマトグラフィー用、25183-1B)
ギ酸(和光純薬工業製、試薬特級、066-00461)
クロロホルム(関東化学製、鹿1級、07278-01)
N−メチル−N’−ニトロ−N−ニトロソグアニジン(関東化学製、鹿1級、25596-51)
t−ブチルメチルエーテル(関東化学製、鹿特級、04418-00)
水酸化ナトリウム(和光純薬工業製、特級、196-13761)
(Sample pretreatment method)
150 mg of alkyl ether carboxylic acid was dissolved in 50 mL of methanol. Moreover, about the cleaning composition, it extract | collected so that it might become 150 mg as alkyl ether carboxylic acid, and melt | dissolved in 50 mL of methanol. In addition, when the detergent composition contained a strong anionic surfactant such as polyoxyethylene alkyl ether sulfate, it was collected so as to be 250 mg or less. Take 1 mL of this solution and apply it to a solid-phase cartridge (Biotage, Isolute SAX, 1 g, 3 mL, 500-0100-B) that has been conditioned in advance with 4 mL of methanol, and collect the passing solution in a 10 mL round bottom test tube. Gathered. Thereafter, elution was performed with 6 mL of a solution obtained by adding 100 mL of methanol to 4.6 g of formic acid, and the eluate was also collected in the same test tube. The collected solution was placed in a block heater heated to 50 ° C., blown with nitrogen gas, concentrated to about 1 mL, and further blown with nitrogen gas at room temperature to dry. Thereto, 2 mL of a diazomethane-ether solution was added, and the mixture was allowed to stand at room temperature for 10 minutes with stirring for derivatization. Thereafter, nitrogen gas was blown at room temperature, and the mixture was concentrated to 500 μL or less, and then chloroform was added to make 500 μL, which was subjected to GC analysis.
In addition, the diazomethane-ether solution was prepared in the following procedures using the diazomethane production | generation apparatus (Miyamoto Riken Kogyo make, GM-50). The first and second receptacles, and the second and third receptacles are connected with a silicone rubber stopper and a Teflon (registered trademark) tube. In a second receiver, 0.8 g of N-methyl-N′-nitro-N-nitrosoguanidine was collected and 2.5 mL of ion exchange water was added. In a third receiver, 10 mL of t-butyl methyl ether was collected. The first, second and third receivers were ice-cooled. Subsequently, a plastic syringe was attached to the second receiver, and 3 mL of a solution in which 20 g of sodium hydroxide was dissolved in 100 mL of ion-exchanged water was placed in this syringe. This sodium hydroxide aqueous solution is slowly added dropwise to produce diazomethane gas, and nitrogen gas is gently blown from the first receiver side, dissolved in t-butyl methyl ether of the third receiver, and diazomethane-ether A solution was obtained.
The following reagents were used in the sample pretreatment.
Methanol (manufactured by Kanto Chemical, for high performance liquid chromatography, 25183-1B)
Formic acid (manufactured by Wako Pure Chemical Industries, reagent special grade, 066-00461)
Chloroform (manufactured by Kanto Chemical, deer grade 1, 07278-01)
N-methyl-N'-nitro-N-nitrosoguanidine (manufactured by Kanto Chemical, deer grade 1, 25596-51)
t-Butyl methyl ether (manufactured by Kanto Chemical, deer special grade, 04418-00)
Sodium hydroxide (Wako Pure Chemical Industries, special grade, 196-13761)

本発明の皮膚洗浄剤組成物に用いる成分(A)のアルキルエーテルカルボン酸は、例えば以下のようにして製造することができる。なお、断りのない限り「%」は質量%を示す。   The alkyl ether carboxylic acid of component (A) used in the skin cleansing composition of the present invention can be produced, for example, as follows. Unless otherwise indicated, “%” indicates mass%.

製造例1
攪拌および温度調節機能を備えたステンレス製オートクレーブに、ラウリルアルコール[商品名:カルコール2098、花王製]1144g(6.14モル)、ミリスチルアルコール[商品名:カルコール4098、花王製]60.2g(0.281モル)、水酸化カリウム2.68g(0.0478モル)を仕込み、減圧脱水を行った。次いで、エチレンオキサイド(EO)996g(22.6モル)を155℃にて導入し、反応温度155℃、反応圧力0.4MPaで2時間反応を行った。反応終了後、80℃、6kPaの減圧条件で30分間攪拌し、未反応のエチレンオキサイドを除去した後、窒素を導入し常圧にし、4.82g(0.0482モル)の90%乳酸をオートクレーブ内に加え、80℃で30分間攪拌し、EO付加モル数3.55モルのアルキルエトキシレート(以下、「生成AE」ともいう)を得た。
攪拌機能、温度調節機能及び酸素ガス導入管を取り付けたガラス製反応容器に、上記生成物90g(0.2モル)と、48%水酸化ナトリウム水溶液16.7g(水酸化ナトリウムとして0.2モル)、パラジウム−白金−ビスマス系触媒(活性炭にパラジウム4%、白金1%及びビスマス5%を担持、含水率50%)0.9g、水494.4gをそれぞれ仕込んだ。攪拌条件下、液温を70℃まで昇温し、酸素を27モル%(対生成AE/時間)の割合で吹き込みながら、反応温度70℃で3.5時間接触酸化反応を行った。反応率は89%であった。
反応終了後、反応液から触媒を濾別し、アルキルエーテルカルボン酸Na塩の水溶液を得た。続いて、35%塩酸を加え、分液操作を実施し、アルキルエーテルカルボン酸を得た。これをEC1とする。
Production Example 1
In a stainless steel autoclave equipped with stirring and temperature control functions, 1144 g (6.14 mol) of lauryl alcohol [trade name: Calcoal 2098, manufactured by Kao], 60.2 g (0 trade name: Calcoal 4098, manufactured by Kao) .281 mol) and 2.68 g (0.0478 mol) of potassium hydroxide were added and dehydration under reduced pressure was performed. Next, 996 g (22.6 mol) of ethylene oxide (EO) was introduced at 155 ° C., and the reaction was carried out at a reaction temperature of 155 ° C. and a reaction pressure of 0.4 MPa for 2 hours. After completion of the reaction, the mixture was stirred for 30 minutes at 80 ° C. under reduced pressure of 6 kPa to remove unreacted ethylene oxide, and then nitrogen was introduced to normal pressure, and 4.82 g (0.0482 mol) of 90% lactic acid was autoclaved. In addition, the mixture was stirred at 80 ° C. for 30 minutes to obtain an alkyl ethoxylate (hereinafter also referred to as “produced AE”) having an EO addition mole number of 3.55 mol.
In a glass reaction vessel equipped with a stirring function, temperature control function and oxygen gas introduction tube, 90 g (0.2 mol) of the above product and 16.7 g of 48% aqueous sodium hydroxide solution (0.2 mol as sodium hydroxide) ), Palladium-platinum-bismuth catalyst (supporting 4% palladium, 1% platinum and 5% bismuth on activated carbon, water content 50%) 0.9 g and 494.4 g water, respectively. Under stirring conditions, the liquid temperature was raised to 70 ° C., and a catalytic oxidation reaction was performed at a reaction temperature of 70 ° C. for 3.5 hours while blowing oxygen at a rate of 27 mol% (vs. production AE / hour). The reaction rate was 89%.
After completion of the reaction, the catalyst was filtered off from the reaction solution to obtain an aqueous solution of alkyl ether carboxylic acid Na salt. Subsequently, 35% hydrochloric acid was added, and a liquid separation operation was performed to obtain an alkyl ether carboxylic acid. This is EC1.

ガスクロマトグラフィーの分析の結果、EC1は、一般式(1)において、M=H、R1はラウリル基/ミリスチル基=95/5、平均炭素数は12.1、nの平均値は2.8、n=0の成分を14.7質量%含み、n=1の成分とn=2の成分の合計量は36.1質量%であった。
また、EO付加モル数の異なる各成分の比率に関しても、R1の組成のうち最大成分の測定値から算出した結果、(n=0成分の質量):(n=1成分の質量):(n=2成分の質量):(n=3成分の質量):(n=4成分の質量)=1:1.22:1.23:1.06:0.83であった。
As a result of analysis by gas chromatography, EC1 is M = H in the general formula (1), R 1 is lauryl group / myristyl group = 95/5, the average carbon number is 12.1, and the average value of n is 2. 8, The component of n = 0 was contained 14.7 mass%, and the total amount of the component of n = 1 and the component of n = 2 was 36.1 mass%.
In addition, regarding the ratio of each component having a different number of EO addition moles, as a result of calculation from the measured value of the maximum component of the R 1 composition, (n = 0 component mass): (n = 1 component mass): ( n = 2 mass of component): (mass of n = 3 component): (mass of n = 4 component) = 1: 1.22: 1.23: 1.06: 0.83.

製造例2
製造例1に倣い、デシルアルコール[商品名:カルコール1098、花王製]、ラウリルアルコール[商品名:カルコール2098、花王製]、ミリスチルアルコール[商品名:カルコール4098、花王製]、セチルアルコール[商品名:カルコール6098、花王製]を質量比10/70/15/5に混合した原料にEOを反応させ、EO付加モル数3.55モルのアルキルエトキシレートを得た。これを製造例1同様、酸化反応を行い、得られたアルキルエーテルカルボン酸塩を塩酸処理することにより、アルキルエーテルカルボン酸を得た。
Production Example 2
Following production example 1, decyl alcohol [trade name: Calcoal 1098, manufactured by Kao], lauryl alcohol [trade name: Calcoal 2098, manufactured by Kao], myristyl alcohol [trade name: Calcoal 4098, manufactured by Kao], cetyl alcohol [trade name] : Calcoal 6098, manufactured by Kao] at a mass ratio of 10/70/15/5 was reacted with EO to obtain an alkyl ethoxylate having 3.55 mol of EO added. This was subjected to an oxidation reaction as in Production Example 1, and the resulting alkyl ether carboxylate was treated with hydrochloric acid to obtain an alkyl ether carboxylic acid.

ガスクロマトグラフィーの分析の結果、一般式(1)において、M=H、R1はデシル基/ラウリル基/ミリスチル基/パルミチル基=10/70/15/5、平均炭素数は12.3、nの平均値は3.3、n=0の成分を15.2質量%含み、n=1の成分とn=2の成分の合計量は31.4質量%であった。
また、EO付加モル数の異なる各成分の比率に関しても、R1の組成のうち最大成分の測定値から算出した結果、(n=0成分の質量):(n=1成分の質量):(n=2成分の質量):(n=3成分の質量):(n=4成分の質量)=1:1.07:1.00:0.85:0.67であった。
As a result of analysis by gas chromatography, in general formula (1), M = H, R 1 is decyl group / lauryl group / myristyl group / palmityl group = 10/70/15/5, average carbon number is 12.3, The average value of n was 3.3 and 15.2% by mass of n = 0 components, and the total amount of n = 1 and n = 2 components was 31.4% by mass.
In addition, regarding the ratio of each component having a different number of EO addition moles, as a result of calculation from the measured value of the maximum component of the R 1 composition, (n = 0 component mass): (n = 1 component mass): ( n = 2 mass of component): (n = mass of 3 component): (mass of n = 4 component) = 1: 1.07: 1.00: 0.85: 0.67.

製造例3
攪拌、温度調節機能を取り付けたガラス製反応容器に、ラウリルアルコール372g(2.00モル)を仕込み、攪拌条件下、液温を70℃まで昇温し、モノクロロ酢酸ナトリウム256g(2.20モル)及び水酸化ナトリウム88g(2.20モル)を分割して加えながら、5時間反応を行った。反応終了後、析出物を濾別し、続いて35%塩酸を加え、酸型化し、アルキルエーテルカルボン酸を得た(一般式(1)において、M=H、R1はラウリル基、n=0)。
Production Example 3
A glass reaction vessel equipped with stirring and temperature control functions was charged with 372 g (2.00 mol) of lauryl alcohol, the temperature was raised to 70 ° C. under stirring conditions, and 256 g (2.20 mol) of sodium monochloroacetate was added. The reaction was carried out for 5 hours while adding 88 g (2.20 mol) of sodium hydroxide in portions. After completion of the reaction, the precipitate was separated by filtration and subsequently acidified by adding 35% hydrochloric acid to obtain an alkyl ether carboxylic acid (in the general formula (1), M = H, R1 is a lauryl group, n = 0 ).

製造例4
製造例1に倣い、デシルアルコールを原料にEOを反応させ、EO付加モル数3.55モルのアルキルエトキシレートを得た。これを製造例1同様、酸化反応を行い、得られたアルキルエーテルカルボン酸塩を塩酸処理することにより、アルキルエーテルカルボン酸を得た。
ガスクロマトグラフィーの分析の結果、一般式(1)において、M=H、R1はデシル基、nの平均値は3.1、n=0の成分を16質量%含み、n=1の成分とn=2の成分の合計量は37質量%であった。
Production Example 4
Following Production Example 1, EO was reacted with decyl alcohol as a raw material to obtain an alkyl ethoxylate having 3.55 moles of EO added. This was subjected to an oxidation reaction as in Production Example 1, and the resulting alkyl ether carboxylate was treated with hydrochloric acid to obtain an alkyl ether carboxylic acid.
As a result of gas chromatography analysis, in general formula (1), M = H, R 1 is a decyl group, n has an average value of 3.1, n = 0 contains 16% by mass, and n = 1 The total amount of n = 2 components was 37% by mass.

製造例5
製造例1に倣い、ラウリルアルコールを原料にEOを反応させ、EO付加モル数3.55モルのアルキルエトキシレートを得た。これを製造例1同様、酸化反応を行い、得られたアルキルエーテルカルボン酸塩を塩酸処理することにより、アルキルエーテルカルボン酸を得た。
ガスクロマトグラフィーの分析の結果、一般式(1)において、M=H、R1はラウリル基、nの平均値は3.1、n=0の成分を16質量%含み、n=1の成分とn=2の成分の合計量は37質量%であった。
Production Example 5
Following Production Example 1, EO was reacted with lauryl alcohol as a raw material to obtain an alkyl ethoxylate having 3.55 moles of EO added. This was subjected to an oxidation reaction as in Production Example 1, and the resulting alkyl ether carboxylate was treated with hydrochloric acid to obtain an alkyl ether carboxylic acid.
As a result of analysis by gas chromatography, in general formula (1), M = H, R 1 is a lauryl group, n has an average value of 3.1, n = 0 contains 16% by mass, and n = 1 The total amount of n = 2 components was 37% by mass.

製造例6
製造例1に倣い、ミリスチルアルコールを原料にEOを反応させ、EO付加モル数3.55モルのアルキルエトキシレートを得た。これを製造例1同様、酸化反応を行い、得られたアルキルエーテルカルボン酸塩を塩酸処理することにより、アルキルエーテルカルボン酸を得た。
ガスクロマトグラフィーの分析の結果、一般式(1)において、M=H、R1はミリスチル基、nの平均値は3.1、n=0の成分を16質量%含み、n=1の成分とn=2の成分の合計量は37質量%であった。
Production Example 6
According to Production Example 1, EO was reacted with myristyl alcohol as a raw material to obtain an alkyl ethoxylate having 3.55 moles of EO added. This was subjected to an oxidation reaction as in Production Example 1, and the resulting alkyl ether carboxylate was treated with hydrochloric acid to obtain an alkyl ether carboxylic acid.
As a result of analysis by gas chromatography, in general formula (1), M = H, R 1 is a myristyl group, n has an average value of 3.1, n = 0 contains 16% by mass, and n = 1 The total amount of n = 2 components was 37% by mass.

製造例7
製造例1に倣い、ラウリルアルコール、セチルアルコールを質量比20/80に混合した原料にEO付加し、EO付加モル数3.55モルのアルキルエトキシレートを得た。これを実施例1同様、酸化反応を行い、得られたアルキルエーテルカルボン酸塩を塩酸処理することにより、アルキルエーテルカルボン酸を得た。
ガスクロマトグラフィーの分析の結果、一般式(1)において、M=H、R1はラウリル基/パルミチル基=20/80、nの平均値は3.1、n=0の成分を16質量%含み、n=1の成分とn=2の成分の合計量は37質量%であった。
Production Example 7
Following Production Example 1, EO was added to a raw material in which lauryl alcohol and cetyl alcohol were mixed at a mass ratio of 20/80 to obtain an alkyl ethoxylate having 3.55 moles of EO added. This was subjected to an oxidation reaction as in Example 1, and the resulting alkyl ether carboxylate was treated with hydrochloric acid to obtain an alkyl ether carboxylic acid.
As a result of analysis by gas chromatography, in general formula (1), M = H, R 1 is lauryl group / palmityl group = 20/80, n average value is 3.1, and n = 0 is 16% by mass. In addition, the total amount of the n = 1 component and the n = 2 component was 37% by mass.

製造例8
製造例1に倣い、ラウリルアルコールを原料にEO反応させ、EO付加モル数4.05モルのアルキルエトキシレートを得た。これを製造例1同様、酸化反応を行い、得られたアルキルエーテルカルボン酸塩を塩酸処理することにより、アルキルエーテルカルボン酸を得た。
Production Example 8
Following Production Example 1, lauryl alcohol was subjected to EO reaction as a raw material to obtain an alkyl ethoxylate having 4.05 moles of EO added. This was subjected to an oxidation reaction as in Production Example 1, and the resulting alkyl ether carboxylate was treated with hydrochloric acid to obtain an alkyl ether carboxylic acid.

ガスクロマトグラフィーの分析の結果、一般式(1)において、M=H、R1はラウリル基、nの平均値は3.5、n=0の成分を11.4質量%含み、n=1の成分とn=2の成分の合計量は30.6質量%であった。
また、EO付加モル数の異なる各成分の比率に関しても、R1の組成のうち最大成分の測定値から算出した結果、(n=0成分の質量):(n=1成分の質量):(n=2成分の質量):(n=3成分の質量):(n=4成分の質量)=1:1.31:1.38:1.25:1.06であった。
As a result of analysis by gas chromatography, in general formula (1), M = H, R 1 is a lauryl group, n has an average value of 3.5, and n = 0 contains 11.4% by mass, n = 1 The total amount of the components and n = 2 was 30.6% by mass.
In addition, regarding the ratio of each component having a different number of EO addition moles, as a result of calculation from the measured value of the maximum component of the R 1 composition, (n = 0 component mass): (n = 1 component mass): ( n = 2 mass of component): (mass of n = 3 component): (mass of n = 4 component) = 1.1.31: 1.38: 1.25: 1.06.

製造例9
攪拌および温度調節機能を備えたステンレス製オートクレーブに、ラウリルアルコール[商品名:カルコール2098、花王製]1144g(6.14モル)、ミリスチルアルコール[商品名:カルコール4098、花王製]60.2g(0.281モル)、水酸化カリウム2.6g(0.0478モル)を仕込み、減圧脱水を行った。次いで、エチレンオキサイド(EO)718g(16.3モル)を155℃にて導入し、反応温度155℃、反応圧力0.4MPaで2時間反応を行った。反応終了後、冷却し、80℃、6kPaの減圧条件で30分間攪拌し、未反応のエチレンオキサイドを除去した後、窒素を導入し常圧にし、4.82g(0.0482モル)の90%乳酸をオートクレーブ内に加え、80℃で30分間攪拌し、EO付加モル数2.55モルのアルキルエトキシレートを得た。
攪拌、温度調節機能を取り付けたガラス製反応容器に、上記生成物600g(2.00モル)を仕込み、攪拌条件下、液温を70℃まで昇温し、モノクロロ酢酸ナトリウム256g(2.20モル)及び水酸化ナトリウム88g(2.20モル)を分割して加えながら、5時間反応を行った。反応終了後、35%塩酸をpHが2.8になるまで加え、酸型化し油層を分取し、アルキルエーテルカルボン酸を得た。これをEC6とする。
Production Example 9
In a stainless steel autoclave equipped with stirring and temperature control functions, 1144 g (6.14 mol) of lauryl alcohol [trade name: Calcoal 2098, manufactured by Kao], 60.2 g (0 trade name: Calcoal 4098, manufactured by Kao) .281 mol) and 2.6 g (0.0478 mol) of potassium hydroxide were added and dehydration under reduced pressure was performed. Subsequently, 718 g (16.3 mol) of ethylene oxide (EO) was introduced at 155 ° C., and the reaction was carried out at a reaction temperature of 155 ° C. and a reaction pressure of 0.4 MPa for 2 hours. After completion of the reaction, the mixture was cooled and stirred at 80 ° C. under a reduced pressure of 6 kPa for 30 minutes to remove unreacted ethylene oxide, then nitrogen was introduced to normal pressure, and 4.82 g (0.0482 mol) of 90% Lactic acid was added to the autoclave and stirred at 80 ° C. for 30 minutes to obtain an alkyl ethoxylate having 2.55 mol of EO added.
A glass reaction vessel equipped with stirring and temperature control functions was charged with 600 g (2.00 mol) of the above product, the temperature of the solution was raised to 70 ° C. under stirring conditions, and 256 g (2.20 mol) of sodium monochloroacetate was added. ) And 88 g (2.20 mol) of sodium hydroxide were added in portions, and the reaction was carried out for 5 hours. After completion of the reaction, 35% hydrochloric acid was added until the pH reached 2.8 to convert it into an acid form, and the oil layer was separated to obtain an alkyl ether carboxylic acid. This is EC6.

ガスクロマトグラフィーの分析の結果、一般式(1)において、M=H、R1はラウリル基/ミリスチル基=94/6、平均炭素数は12.1、nの平均値は3.1、n=0の成分を9.9質量%含み、n=1の成分とn=2の成分の合計量は35.4質量%であった。
また、EO付加モル数の異なる各成分の比率に関しても、R1の組成のうち最大成分の測定値から算出した結果、(n=0成分の質量):(n=1成分の質量):(n=2成分の質量):(n=3成分の質量):(n=4成分の質量)=1:1.65:1.92:1.74:1.32であった。
As a result of analysis by gas chromatography, in general formula (1), M = H, R 1 is lauryl group / myristyl group = 94/6, average carbon number is 12.1, average value of n is 3.1, n = 0% component was included, and the total amount of the n = 1 component and the n = 2 component was 35.4% by mass.
In addition, regarding the ratio of each component having a different number of EO addition moles, as a result of calculation from the measured value of the maximum component of the composition of R1, (n = 0 component mass): (n = 1 component mass): (n = Mass of 2 components) :( mass of n = 3 components) :( mass of n = 4 components) = 1: 1.65: 1.92: 1.74: 1.32.

後述する実施例において、EC2に関しては、製造例5、製造例6、製造例7で得られたアルキルエーテルカルボン酸を、各々質量割合で78.75/15/6.25の比で混合し、EC2とした。   In the examples to be described later, regarding EC2, the alkyl ether carboxylic acids obtained in Production Example 5, Production Example 6 and Production Example 7 are mixed at a mass ratio of 78.75 / 15 / 6.25, respectively. EC2.

後述する実施例において、EC3に関しては、製造例2、製造例3で得られたアルキルエーテルカルボン酸を、各々質量割合で90/10の比で混合し、EC3とした。   In the examples described later, regarding EC3, the alkyl ether carboxylic acids obtained in Production Example 2 and Production Example 3 were mixed at a mass ratio of 90/10 to obtain EC3.

後述する実施例において、EC4に関しては、製造例1で得られたEC1と製造例4で得られたアルキルエーテルカルボン酸を、各々質量割合で40/60の比で混合し、EC4とした。   In the examples described later, regarding EC4, EC1 obtained in Production Example 1 and the alkyl ether carboxylic acid obtained in Production Example 4 were mixed in a mass ratio of 40/60 to obtain EC4.

後述する実施例において、EC5に関しては、製造例2、製造例8で得られたアルキルエーテルカルボン酸を、各々質量割合で40/60の比で混合し、EC5とした。   In the examples described later, regarding EC5, the alkyl ether carboxylic acids obtained in Production Example 2 and Production Example 8 were mixed at a mass ratio of 40/60 to obtain EC5.

実施例1〜13、比較例1〜5
表2〜5に示す組成の皮膚洗浄剤組成物を製造し、泡の弾力性及びつっぱり感のなさを評価した。結果を表2〜5に併せて示す。
なお、実施例で使用した成分(A)の構成は、表1に示すとおりである。
Examples 1-13, Comparative Examples 1-5
Skin cleansing compositions having the compositions shown in Tables 2 to 5 were produced, and the elasticity of the foam and the lack of feeling of tension were evaluated. The results are shown in Tables 2 to 5.
In addition, the structure of the component (A) used in the Examples is as shown in Table 1.

(製造方法)
成分(E)精製水(成分(C)の5倍量に相当する成分(E)を除いたもの)に成分(D)を添加し、溶解した後75℃に加温した。この水溶液に、成分(A)および(B)を70℃で溶解し、混合した液を添加し、均一になるまで攪拌した。その後、必要に応じて、成分(F)を加え、均一になるまで攪拌し、25℃まで冷却した。次に、成分(C)の5倍量に相当する成分(E)と成分(C)を混合したものを添加し、均一になるまで攪拌して、皮膚洗浄剤組成物を得た。
(Production method)
Component (D) was added to component (E) purified water (excluding component (E) corresponding to 5 times the amount of component (C)), dissolved, and heated to 75 ° C. Components (A) and (B) were dissolved in this aqueous solution at 70 ° C., and the mixed solution was added and stirred until uniform. Thereafter, if necessary, component (F) was added, stirred until uniform, and cooled to 25 ° C. Next, what mixed the component (E) and component (C) equivalent to 5 times the amount of a component (C) was added, it stirred until it became uniform, and the skin cleansing composition was obtained.

(評価方法)
(1)泡の弾力性:
泡立てネット[白元社製]を水(約8g)で湿らせた後、洗浄剤1gを泡立てネット上に載せた。泡立てネットを両手のひらで包み込み、40回円を描くように両手のひらをこすり合わせて泡立てた。
泡立てた泡をシャーレ(直径6.6cm、高さ1.8cm)に集め、定規で液面とシャーレの高さが一致して平らになるように過剰な泡を取り除いた。泡の弾力性の測定には、FUDOH レオメーター RTC(不動工業社製)を用い、専用アダプター3(圧縮弾性測定アダプター Dφ=5)を用いた。シャーレ上の泡表面に、アダプターを設置し、サンプリング周期0.1秒、ストローク20mm、スピード30cm/分、表示をg単位とし、泡の液温約25℃にて、ストローク方向を上下に設定して、アダプターにかかる応力を測定した。得られた測定値のうち、最もアダプターに負荷がかかったときの数値を、弾力とし、レオメーターに表示された数値を表に示す。
(Evaluation method)
(1) Bubble elasticity:
After the foaming net [manufactured by Hakugen Co., Ltd.] was moistened with water (about 8 g), 1 g of the cleaning agent was placed on the foaming net. The whipping net was wrapped in the palms of both hands, and the palms of both hands were rubbed together to draw a circle 40 times.
The foamed foam was collected in a petri dish (diameter 6.6 cm, height 1.8 cm), and excess foam was removed with a ruler so that the liquid surface and the petri dish were flush with each other. For the measurement of foam elasticity, a FUDOH rheometer RTC (manufactured by Fudo Kogyo Co., Ltd.) was used, and a dedicated adapter 3 (compression elasticity measurement adapter Dφ = 5) was used. Install the adapter on the surface of the foam on the petri dish, set the sampling direction to 0.1 seconds, the stroke 20 mm, the speed 30 cm / min, the display in g, the foam liquid temperature about 25 ° C, and the stroke direction up and down. Then, the stress applied to the adapter was measured. Among the measured values, the numerical value when the adapter is most loaded is the elasticity, and the numerical value displayed on the rheometer is shown in the table.

(2)つっぱり感のなさ:
専門パネリスト5名に、各皮膚洗浄剤組成物1gを用いて洗顔させ、水ですすいだ後、タオルドライ直後のつっぱり感を、以下の基準で官能評価させ、その合計点を求めた。
3;つっぱらない。
2;ほとんどつっぱらない。
1;ややつっぱる。
0;つっぱる。
(2) No sense of tension:
Five professional panelists washed their face with 1 g of each skin cleanser composition, rinsed with water, and then sensory-evaluated the feeling of squeezing immediately after towel drying based on the following criteria to determine the total score.
3; It's not tangled.
2;
1;
0;

Figure 2013139439
Figure 2013139439

Figure 2013139439
Figure 2013139439

Figure 2013139439
Figure 2013139439

Figure 2013139439
Figure 2013139439

Figure 2013139439
Figure 2013139439

実施例14
以下に示す組成の皮膚洗浄剤組成物を、実施例1〜15と同様にして製造した。
(成分) (質量%)
EC6 8
ミリスチン酸 2
パルミチン酸 4
ステアリン酸 2
ベヘニン酸 2
ジアリルジアルキル四級アンモニウム塩/アクリルアミド/
アクリル酸共重合体*1 1
ラウリルヒドロキシスルホベタイン*2 3
グリセリン 10
水酸化カリウム 3.1
水 残部
合計 100

*1:マーコート プラス 3331(Lubrizol Advanced Materials, Inc.)
*2:アンヒトール20HD(花王)の有効成分
得られた皮膚洗浄剤組成物は、泡質がキメ細かく弾力性に優れ、洗い上がりの肌がしっとりしてつっぱり感が感じられないものであった。
Example 14
Skin cleansing compositions having the following compositions were produced in the same manner as in Examples 1-15.
(Ingredient) (mass%)
EC6 8
Myristic acid 2
Palmitic acid 4
Stearic acid 2
Behenic acid 2
Diallyldialkyl quaternary ammonium salt / acrylamide /
Acrylic acid copolymer * 1 1
Lauryl hydroxysulfobetaine * 2 3
Glycerin 10
Potassium hydroxide 3.1
Water balance
Total 100

* 1: Marcote Plus 3331 (Lubrizol Advanced Materials, Inc.)
* 2: Active ingredient of Amphital 20HD (Kao) The obtained skin cleanser composition had fine foam and excellent elasticity, and the washed-out skin was moist and did not feel a firm feeling.

実施例15
以下に示す組成の皮膚洗浄剤組成物を、実施例1〜15と同様にして製造した。
(成分) (質量%)
EC1 8
パルミチン酸 4
ステアリン酸 4
塩化O−[2−ヒドロキシ−3−(トリメチルアンモニオ)プロピル]
グァーガム*3 0.5
グリセリンモノ−2−エチルヘキシルエーテル液*4 3
ソルビトール 20
水酸化カリウム 2.4
水 残部
合計 100

*3:ジャガー C−17K(Rhodia Operations(Novecare))
*4:ペネトール GE-EH(花王)の有効成分
得られた皮膚洗浄剤組成物は、泡質がキメ細かく弾力性に優れ、洗い上がりの肌がしっとりしてつっぱり感が感じられないものであった。
Example 15
Skin cleansing compositions having the following compositions were produced in the same manner as in Examples 1-15.
(Ingredient) (mass%)
EC1 8
Palmitic acid 4
Stearic acid 4
O- [2-hydroxy-3- (trimethylammonio) propyl] chloride
Guar gum * 3 0.5
Glycerin mono-2-ethylhexyl ether solution * 4 3
Sorbitol 20
Potassium hydroxide 2.4
Water balance
Total 100

* 3: Jaguar C-17K (Rhodia Operations (Novecare))
* 4: Active ingredient of Penetol GE-EH (Kao) The obtained skin cleanser composition has fine foam and excellent elasticity, and the washed-out skin is moist and does not feel a firm feeling. .

Claims (12)

次の成分(A)、(B)、(C)、(D)及び(E):
(A)一般式(1)
Figure 2013139439
(式中、R1は炭素数4〜22のアルキル基を示し、nは0〜20の数を示す)
で表されるアルキルエーテルカルボン酸であって、R1の平均炭素数が10.8〜12.8であり、n=0の成分を4.3〜30質量%含み、n=1の成分とn=2の成分の合計含有量が20質量%以上40質量%未満であるアルキルエーテルカルボン酸 1〜20質量%、
(B)一般式(2)
Figure 2013139439
(式中、R2は炭素数9〜21の直鎖又は分岐鎖のアルキル基又はアルケニル基を示す)
で表される脂肪酸 1〜20質量%、
(C)カチオンポリマー 0.1〜5質量%、
(D)塩基、
(E)水
を含有し、成分(A)及び(B)は、少なくとも一部が成分(D)と塩で存在し、成分(D)は、成分(A)及び(B)に対するモル比(成分(D)/(成分(A)+成分(B))が0.9〜1.1である皮膚洗浄剤組成物。
The following components (A), (B), (C), (D) and (E):
(A) General formula (1)
Figure 2013139439
(In the formula, R 1 represents an alkyl group having 4 to 22 carbon atoms, and n represents a number of 0 to 20).
Wherein R 1 has an average carbon number of 10.8 to 12.8, 4.3 to 30% by mass of n = 0, and n = 1 1-20% by mass of an alkyl ether carboxylic acid having a total content of n = 2 components of 20% by mass or more and less than 40% by mass,
(B) General formula (2)
Figure 2013139439
(Wherein R 2 represents a linear or branched alkyl or alkenyl group having 9 to 21 carbon atoms)
1 to 20% by mass of a fatty acid represented by
(C) Cationic polymer 0.1-5% by mass,
(D) a base,
(E) It contains water, and components (A) and (B) are at least partially present as component (D) and salt, and component (D) is a molar ratio of components (A) and (B) ( Skin cleanser composition whose component (D) / (component (A) + component (B)) is 0.9-1.1.
さらに、(F)ポリオールを含有する請求項1記載の皮膚洗浄剤組成物。   The skin cleanser composition according to claim 1, further comprising (F) a polyol. 成分(B)が、一般式(2)中、R2の炭素数が15〜21の脂肪酸を40〜100質量%含むものである請求項1又は2記載の皮膚洗浄剤組成物。 Component (B), the general formula (2) in claim 1 or 2 skin cleansing composition according the number of carbon atoms in R 2 is intended to include 40 to 100 wt% of the fatty acids of 15 to 21. 成分(A)及び(B)の酸としての質量割合が、(A)/(B)=0.3〜5である請求項1〜3のいずれか1項記載の皮膚洗浄剤組成物。   The skin cleansing composition according to any one of claims 1 to 3, wherein a mass ratio of the components (A) and (B) as an acid is (A) / (B) = 0.3 to 5. 成分(A)において、一般式(1)中、nの平均値(平均付加モル数)が1.5〜10である請求項1〜4のいずれか1項記載の皮膚洗浄剤組成物。   In component (A), the average value (average addition mole number) of n is 1.5-10 in general formula (1), The skin cleanser composition of any one of Claims 1-4. 成分(A)において、一般式(1)中、R1が炭素数6〜20のアルキル基であり、nの平均値が2.5〜4.5であり、n=0の成分を9.6〜27質量%含む請求項1〜5のいずれか1項記載の皮膚洗浄剤組成物。 In the component (A), in the general formula (1), R 1 is an alkyl group having 6 to 20 carbon atoms, an average value of n is 2.5 to 4.5, and a component of n = 0 is 9. The skin cleanser composition according to any one of claims 1 to 5, comprising 6 to 27% by mass. 成分(A)において、一般式(1)中、R1が炭素数8〜18のアルキル基であり、nの平均値が2.5〜3.4であり、n=0の成分を9.6〜27質量%含む請求項1〜6のいずれか1項記載の皮膚洗浄剤組成物。 In the component (A), in the general formula (1), R 1 is an alkyl group having 8 to 18 carbon atoms, the average value of n is 2.5 to 3.4, and the component of n = 0 is 9. The skin cleanser composition according to any one of claims 1 to 6, comprising 6 to 27% by mass. 成分(A)において、一般式(1)中、R1が炭素数8〜16のアルキル基であり、nの平均値が2.8〜3.4であり、n=0の成分を9.6〜27質量%、n=1の成分とn=2の成分を合計で27〜36.5質量%含む請求項1〜7のいずれか1項記載の皮膚洗浄剤組成物。 In the component (A), in the general formula (1), R 1 is an alkyl group having 8 to 16 carbon atoms, an average value of n is 2.8 to 3.4, and a component of n = 0 is 9. The skin cleansing composition according to any one of claims 1 to 7, comprising 6 to 27% by mass, and 27 to 36.5% by mass in total of a component of n = 1 and a component of n = 2. 成分(A)において、一般式(1)中、(n=0成分の質量):(n=1成分の質量):(n=2成分の質量):(n=3成分の質量):(n=4成分の質量)=1:0.99〜3.50:0.89〜3.00:0.76〜3.00:0.63〜1.6となる請求項1〜8のいずれか1項記載の皮膚洗浄剤組成物。   In component (A), in general formula (1), (mass of n = 0 component): (mass of n = 1 component): (mass of n = 2 component): (mass of n = 3 component): ( n = mass of four components) = 1: 0.99 to 3.50: 0.89 to 3.00: 0.76 to 3.00: 0.63 to 1.6 A skin cleanser composition according to claim 1. 成分(A)において、一般式(1)中、R1が2種以上のアルキル基を含み、一番含有量の多いアルキル鎖長を有する成分が55質量%以上97質量%未満である請求項1〜9のいずれか1項記載の皮膚洗浄剤組成物。 In component (A), in general formula (1), R 1 contains two or more alkyl groups, and the component having the largest alkyl chain length is 55% by mass or more and less than 97% by mass. The skin cleansing composition according to any one of 1 to 9. 成分(A)において、一般式(1)中、n=0の成分を8質量%以上12質量%未満含み、(n=0成分の質量):(n=1成分の質量):(n=2成分の質量):(n=3成分の質量):(n=4成分の質量)=1:1.53〜1.87:1.59〜2.25:1.33〜2.16:1.14〜1.52となるか、又は、n=0の成分を12質量%以上17質量%以下含み、(n=0成分の質量):(n=1成分の質量):(n=2成分の質量):(n=3成分の質量):(n=4成分の質量)=1:0.99〜1.34:0.89〜1.40:0.76〜1.23:0.63〜0.99となる請求項1〜10のいずれか1項記載の皮膚洗浄剤組成物。   In the component (A), in the general formula (1), the component of n = 0 is contained in an amount of 8% by mass or more and less than 12% by mass, (n = 0 component mass): (n = 1 component mass): (n = 2 component mass): (n = 3 component mass): (n = 4 component mass) = 1.1.53-1.87: 1.59-2.25: 1.33-2.16: 1.14 to 1.52, or 12 to 17% by mass of n = 0 component, (n = 0 component mass): (n = 1 component mass): (n = 2 component mass): (n = 3 component mass): (n = 4 component mass) = 1: 0.99 to 1.34: 0.89 to 1.40: 0.76 to 1.23: The skin cleansing composition according to any one of claims 1 to 10, which is 0.63 to 0.99. 請求項1〜11のいずれか1項記載の皮膚洗浄剤組成物を、身体皮膚部に適用して洗浄した後、すすぐ皮膚洗浄方法。   A method for rinsing the skin after applying the skin cleansing composition according to any one of claims 1 to 11 to a body skin part and cleaning the body skin part.
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