JP2015229650A - Skin cleansing composition - Google Patents
Skin cleansing composition Download PDFInfo
- Publication number
- JP2015229650A JP2015229650A JP2014116663A JP2014116663A JP2015229650A JP 2015229650 A JP2015229650 A JP 2015229650A JP 2014116663 A JP2014116663 A JP 2014116663A JP 2014116663 A JP2014116663 A JP 2014116663A JP 2015229650 A JP2015229650 A JP 2015229650A
- Authority
- JP
- Japan
- Prior art keywords
- mass
- component
- foam
- preferable
- alkyl
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
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- 239000000203 mixture Substances 0.000 title claims abstract description 134
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 88
- -1 alkyl ether carboxylic acid Chemical class 0.000 claims abstract description 61
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims abstract description 26
- 229910052799 carbon Inorganic materials 0.000 claims abstract description 24
- 229920002678 cellulose Polymers 0.000 claims abstract description 18
- 239000001913 cellulose Substances 0.000 claims abstract description 18
- 229920000642 polymer Polymers 0.000 claims abstract description 16
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims abstract description 15
- 150000003839 salts Chemical class 0.000 claims abstract description 13
- 239000002280 amphoteric surfactant Substances 0.000 claims abstract description 9
- 229910052783 alkali metal Inorganic materials 0.000 claims abstract description 6
- 150000001340 alkali metals Chemical class 0.000 claims abstract description 6
- 229910052784 alkaline earth metal Inorganic materials 0.000 claims abstract description 5
- 150000001342 alkaline earth metals Chemical class 0.000 claims abstract description 5
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 43
- 239000000194 fatty acid Substances 0.000 claims description 43
- 229930195729 fatty acid Natural products 0.000 claims description 43
- 150000004665 fatty acids Chemical class 0.000 claims description 43
- 125000004432 carbon atom Chemical group C* 0.000 claims description 32
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 11
- 229920006322 acrylamide copolymer Polymers 0.000 claims description 10
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 claims description 9
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- 235000010417 guar gum Nutrition 0.000 claims description 8
- 239000000665 guar gum Substances 0.000 claims description 8
- 229960002154 guar gum Drugs 0.000 claims description 8
- 150000003242 quaternary ammonium salts Chemical class 0.000 claims description 8
- 125000003342 alkenyl group Chemical group 0.000 claims description 6
- 235000010491 tara gum Nutrition 0.000 claims description 4
- 239000000213 tara gum Substances 0.000 claims description 4
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- 239000000711 locust bean gum Substances 0.000 claims description 3
- 235000001019 trigonella foenum-graecum Nutrition 0.000 claims description 3
- 125000001453 quaternary ammonium group Chemical group 0.000 claims 1
- 239000006260 foam Substances 0.000 abstract description 96
- 238000005187 foaming Methods 0.000 abstract description 29
- 238000004519 manufacturing process Methods 0.000 description 31
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 30
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- 238000006243 chemical reaction Methods 0.000 description 20
- 238000004140 cleaning Methods 0.000 description 19
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- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 14
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 13
- 238000005406 washing Methods 0.000 description 13
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 12
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- KWIUHFFTVRNATP-UHFFFAOYSA-N Betaine Natural products C[N+](C)(C)CC([O-])=O KWIUHFFTVRNATP-UHFFFAOYSA-N 0.000 description 10
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- KWIUHFFTVRNATP-UHFFFAOYSA-O N,N,N-trimethylglycinium Chemical compound C[N+](C)(C)CC(O)=O KWIUHFFTVRNATP-UHFFFAOYSA-O 0.000 description 10
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- 235000011121 sodium hydroxide Nutrition 0.000 description 8
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- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 7
- 238000007254 oxidation reaction Methods 0.000 description 7
- XDOFQFKRPWOURC-UHFFFAOYSA-N 16-methylheptadecanoic acid Chemical compound CC(C)CCCCCCCCCCCCCCC(O)=O XDOFQFKRPWOURC-UHFFFAOYSA-N 0.000 description 6
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 description 6
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 6
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 6
- 229910052700 potassium Inorganic materials 0.000 description 6
- 239000011591 potassium Substances 0.000 description 6
- 239000011734 sodium Substances 0.000 description 6
- 229910052708 sodium Inorganic materials 0.000 description 6
- 238000012360 testing method Methods 0.000 description 6
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- 238000004364 calculation method Methods 0.000 description 5
- 210000000245 forearm Anatomy 0.000 description 5
- 235000011187 glycerol Nutrition 0.000 description 5
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 description 5
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- 229920003088 hydroxypropyl methyl cellulose Polymers 0.000 description 5
- UFVKGYZPFZQRLF-UHFFFAOYSA-N hydroxypropyl methyl cellulose Chemical compound OC1C(O)C(OC)OC(CO)C1OC1C(O)C(O)C(OC2C(C(O)C(OC3C(C(O)C(O)C(CO)O3)O)C(CO)O2)O)C(CO)O1 UFVKGYZPFZQRLF-UHFFFAOYSA-N 0.000 description 5
- 239000007788 liquid Substances 0.000 description 5
- 239000002994 raw material Substances 0.000 description 5
- PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 description 4
- SVTBMSDMJJWYQN-UHFFFAOYSA-N 2-methylpentane-2,4-diol Chemical compound CC(O)CC(C)(C)O SVTBMSDMJJWYQN-UHFFFAOYSA-N 0.000 description 4
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 4
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 4
- 239000002253 acid Substances 0.000 description 4
- 150000001408 amides Chemical class 0.000 description 4
- MWKFXSUHUHTGQN-UHFFFAOYSA-N decan-1-ol Chemical compound CCCCCCCCCCO MWKFXSUHUHTGQN-UHFFFAOYSA-N 0.000 description 4
- 229910001873 dinitrogen Inorganic materials 0.000 description 4
- 238000001035 drying Methods 0.000 description 4
- BXWNKGSJHAJOGX-UHFFFAOYSA-N hexadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 description 4
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 4
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 4
- 125000001421 myristyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 4
- 229910052757 nitrogen Inorganic materials 0.000 description 4
- HLZKNKRTKFSKGZ-UHFFFAOYSA-N tetradecan-1-ol Chemical compound CCCCCCCCCCCCCCO HLZKNKRTKFSKGZ-UHFFFAOYSA-N 0.000 description 4
- 230000008719 thickening Effects 0.000 description 4
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- DDGPBVIAYDDWDH-UHFFFAOYSA-N 3-[dodecyl(dimethyl)azaniumyl]-2-hydroxypropane-1-sulfonate Chemical compound CCCCCCCCCCCC[N+](C)(C)CC(O)CS([O-])(=O)=O DDGPBVIAYDDWDH-UHFFFAOYSA-N 0.000 description 3
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- FPVVYTCTZKCSOJ-UHFFFAOYSA-N Ethylene glycol distearate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCCOC(=O)CCCCCCCCCCCCCCCCC FPVVYTCTZKCSOJ-UHFFFAOYSA-N 0.000 description 3
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- 230000000052 comparative effect Effects 0.000 description 3
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Landscapes
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Abstract
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.
従来、洗浄性や泡質、なめらかな感触等に優れた洗浄剤組成物が検討されている。
例えば、特許文献1には、特定の両性界面活性剤及びカチオン性糖誘導体を含有する洗浄剤組成物が、洗浄時に豊かで滑らかな泡を実現し、すすぎ時にはすすぎ性とすべり性を与えるとともに、使用後には適度な後残り感、滑らかさ、潤い感が得られる洗浄剤組成物が記載されている。また、特許文献2には、特定のアルキルエーテルカルボン酸又はその塩、ヒドロキシエチル基又はヒドロキシプロピル基が付加したセルロース、アニオン界面活性剤を含有する皮膚洗浄剤組成物が、泡立ちに優れ、泡に厚み感が出て、洗浄時に肌がやわらかく感じられ、優しさが実感できることが記載されている。さらに、特許文献3には、特定のアルキルエーテルカルボン酸、脂肪酸、中和剤を特定の割合で含有する皮膚洗浄剤組成物が、泡質、泡量及びすすぎ性に優れ、洗浄力が高いことが記載されている。
Conventionally, a detergent composition excellent in detergency, foam quality, smooth feel and the like has been studied.
For example, in Patent Document 1, a detergent composition containing a specific amphoteric surfactant and a cationic sugar derivative realizes a rich and smooth foam at the time of washing, and provides rinsing properties and sliding properties at the time of rinsing, A detergent composition is described that provides an after-feel, smoothness and moist feeling after use. Further, in Patent Document 2, a skin cleansing composition containing a specific alkyl ether carboxylic acid or a salt thereof, a cellulose to which a hydroxyethyl group or a hydroxypropyl group is added, and an anionic surfactant is excellent in foaming and foam. It is described that a feeling of thickness comes out, the skin feels soft during washing, and gentleness can be realized. Furthermore, Patent Document 3 discloses that a skin cleanser composition containing a specific alkyl ether carboxylic acid, a fatty acid, and a neutralizer in a specific ratio is excellent in foam quality, amount of foam and rinsing properties, and has a high detergency. Is described.
従来の皮膚洗浄剤組成物は、洗浄性やすすぎ性等の機能面に開発の主眼がおかれていた。しかし、近年、要求特性や健康意識の高まりから、上記の洗浄剤としての機能的な面に加え、使用時におけるイメージ(やわらかい肌やなめらかな肌の実感)といった付加価値が要求されるようになってきた。
本発明は、洗浄時の泡立ちや泡の厚み感、とろみ感に優れ、すすぎ時のなめらかさ及びストップフィーリングに優れ、すすぎ後に残留感がなく、しっとり感が得られる皮膚洗浄剤組成物に関する。
Conventional skin cleansing compositions have been focused on development in terms of functions such as cleanability and rinsability. However, in recent years, due to the increase in required characteristics and health consciousness, in addition to the above functional aspects as a cleaning agent, added value such as an image at the time of use (feeling of soft skin and smooth skin) has been required. I came.
The present invention relates to a skin cleanser composition that is excellent in foaming, foam thickness and thickness during washing, excellent in smoothness and stop feeling during rinsing, has no residual feeling after rinsing, and provides a moist feeling.
本発明者らは、特定の分布を有するアルキルエーテルカルボン酸又はその塩と、脂肪酸、両性界面活性剤、特定の3種のポリマーを組み合わせた皮膚洗浄剤組成物が、洗浄時の泡立ちや泡の厚み感、とろみ感に優れ、すすぎ時のなめらかさ及びストップフィーリングに優れ、すすぎ後に残留感がなく、しっとり感が得られることを見出した。 The inventors of the present invention have developed a skin cleansing composition comprising a combination of an alkyl ether carboxylic acid having a specific distribution or a salt thereof, a fatty acid, an amphoteric surfactant, and a specific three types of polymers. It has been found that it has excellent thickness and thickness, is excellent in smoothness and stop feeling during rinsing, has no residual feeling after rinsing, and has a moist feeling.
本発明は、次の成分(A)、(B)、(C)及び(D):
(A)一般式(1)
The present invention includes the following components (A), (B), (C) and (D):
(A) General formula (1)
(式中、R1は炭素数4〜22のアルキル基を示し、nは0〜20の数を示し、Mは水素原子、アルカリ金属、アルカリ土類金属、アンモニウム又は有機アンモニウムを示す)
で表されるアルキルエーテルカルボン酸又はその塩であって、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の成分を合計で40質量%未満含むアルキルエーテルカルボン酸又はその塩 1〜8質量%、
(B)一般式(2)
(In the formula, R 1 represents an alkyl group having 4 to 22 carbon atoms, n represents a number of 0 to 20, and M represents a hydrogen atom, an alkali metal, an alkaline earth metal, ammonium, or organic ammonium).
Wherein R 1 has an average carbon number of 10.8 to 12.8, contains 4.3 to 30% by mass of n = 0, and n = 1 An alkyl ether carboxylic acid or a salt thereof containing 1 to 8% by mass,
(B) General formula (2)
(式中、R2は炭素数9〜21のアルキル基又はアルケニル基を示し、R2は少なくとも炭素数11のアルキル基を含み、R2の平均炭素数は11〜15である)
で表される脂肪酸 8〜16質量%、
(C)両性界面活性剤 0.5〜7質量%、
(D1)電荷密度が0.5〜4.5meq/gのカチオン化ポリマー、
(D2)ノニオン性のガム類、
(D3)ヒドロキシエチル基又はヒドロキシプロピル基が付加したノニオン性セルロース
を含有し、全脂肪酸に対する炭素数11のアルキル基を有する脂肪酸の質量割合(炭素数11のアルキル基を有する脂肪酸/全脂肪酸)が、0.5〜1である皮膚洗浄剤組成物に関する。
(Wherein R 2 represents an alkyl group or alkenyl group having 9 to 21 carbon atoms, R 2 includes at least an alkyl group having 11 carbon atoms, and R 2 has an average carbon number of 11 to 15)
8 to 16% by mass of a fatty acid represented by
(C) Amphoteric surfactant 0.5-7% by mass,
(D1) a cationized polymer having a charge density of 0.5 to 4.5 meq / g,
(D2) nonionic gums,
(D3) Nonionic cellulose to which hydroxyethyl group or hydroxypropyl group is added, and the mass ratio of fatty acids having 11 alkyl groups to all fatty acids (fatty acids having 11 alkyl groups / total fatty acids) is , 0.5 to 1 for a skin cleanser composition.
本発明の皮膚洗浄剤組成物は、洗浄時の泡立ちや泡の厚み感、とろみ感に優れ、すすぎ時のなめらかさ及びストップフィーリングに優れ、すすぎ後に残留感がなく、しっとり感が得られる皮膚洗浄剤組成物を提供する。
本発明の皮膚洗浄剤組成物の特徴の一つが、とろみ感のある泡を提供できることにある。従来の皮膚洗浄剤組成物は、ゆっくり広げたときには動きやすい泡であっても、実際の使用時のように素早く泡を広げるような条件では、さらに泡が動きやすくなるために泡を感じる度合いが減少してしまうものであった。しかし、本発明においては、素早く泡を広げた場合にも、泡の重さと泡のボリューム感が増し(泡の存在感が増すため)、すべりが良くとろみのあるなめらかな泡で全身を洗浄することができ、うるおいのあるなめらかな肌で、やわらかい肌を実感することができるものである。
すなわち、本発明において、とろみ感ある泡とは、皮膚上に泡をゆっくり拡げると泡が動きやすいが、すばやく広げた時には、泡のボリューム感が増し、泡が動きにくくなることを意味する。
The skin cleansing composition of the present invention has excellent foaming and foam thickness feeling during washing, thickness, excellent smoothness and stop feeling during rinsing, no residual feeling after rinsing, and a moist feeling. A cleaning composition is provided.
One of the features of the skin cleansing composition of the present invention is that it can provide thick foam. Even if the conventional skin cleansing composition is a foam that is easy to move when spread slowly, under the conditions that the foam is spread quickly as in actual use, the foam is more likely to move and the degree of feeling of the foam It was a decrease. However, in the present invention, even when the foam is quickly expanded, the weight of the foam and the volume of the foam increase (because of the presence of the foam), and the whole body is washed with a smooth, thick and smooth foam. It is possible to feel soft skin with moist and smooth skin.
That is, in the present invention, the thick foam means that the foam is easy to move when the foam is slowly spread on the skin, but when the foam is spread quickly, the volume of the foam is increased and the foam becomes difficult to move.
本発明で用いる成分(A)のアルキルエーテルカルボン酸又はその塩は、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のアルキル基が好ましく、炭素数8〜16、更には炭素数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であり、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) or a salt thereof 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, more preferably an alkyl group having 8 to 18 carbon atoms, 8 to 16 carbon atoms, and further 10 to 10 carbon atoms. 16 alkyl groups are more preferred. 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. The average carbon number of R 1 is 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すが、成分(A)の組成中の平均付加モル数(nの平均値)は、泡立ちが良好である点から、1.5〜10が好ましく、2.5〜6.4がより好ましく、2.5〜3.7がさらに好ましく、2.5〜3.4がさらに好ましく、2.8〜3.4がさらに好ましく、2.8〜3.1がさらに好ましい。
成分(A)のアルキルエーテルカルボン酸又はその塩は、一般式(1)において、n=0の成分を4.3〜30質量%、好ましくは4.9〜27質量%、より好ましくは9.6〜27質量%、さらに好ましくは、9.6質量%を超え27質量%以下、また、好ましくは9.8〜27質量%、より好ましくは9.9〜27質量%、更に好ましくは9.9〜16質量%、より好ましくは9.9〜15質量%含むものである。この範囲内とすることにより、泡量、泡質に優れる。
さらに、n=1の成分とn=2の成分を合計で40質量%未満含み、好ましくは21質量%以上40質量%未満、より好ましくは27〜37質量%、さらに好ましくは27〜36.5質量%、さらにより好ましくは35〜36.1質量%含むのが、泡質、泡量の観点から好ましい。
Moreover, in formula, n shows the number of 0-20, and 0-12 are more preferable. In addition, although n shows the addition mole number of ethylene oxyoxide, the average addition mole number (average value of n) in a composition of a component (A) is 1.5-10 from the point that foaming is favorable. Preferably, 2.5 to 6.4 is more preferable, 2.5 to 3.7 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) or a salt thereof is 4.3 to 30% by mass, preferably 4.9 to 27% by mass, more preferably 9. 6 to 27% by mass, more preferably more than 9.6% by mass and 27% by mass or less, preferably 9.8 to 27% by mass, more preferably 9.9 to 27% by mass, and still more preferably 9. 9 to 16% by mass, more preferably 9.9 to 15% by mass. By setting it within this range, the foam amount and foam quality are excellent.
Furthermore, it contains less than 40% by mass in total of n = 1 component and n = 2 component, preferably 21% by mass or more and less than 40% by mass, more preferably 27-37% by mass, and further preferably 27-36.5%. It is preferable from a viewpoint of foam quality and the amount of foam to contain 35 mass%, and still more preferably 35-36.1 mass%.
また、式中、Mとしては、水素原子;ナトリウム、カリウム等のアルカリ金属;カルシウム、マグネシウム等のアルカリ土類金属;アンモニウム;モノエタノールアミン、ジエタノールアミン、トリエタノールアミン等のアルカノールアミン由来のアンモニウムなどが挙げられる。これらの中で、起泡性、低温安定性、経時での着色のなさの点から、アルカリ金属が好ましい。 In the formula, M represents a hydrogen atom; an alkali metal such as sodium or potassium; an alkaline earth metal such as calcium or magnesium; an ammonium; an ammonium derived from an alkanolamine such as monoethanolamine, diethanolamine or triethanolamine; Can be mentioned. Among these, alkali metals are preferable from the viewpoints of foamability, low-temperature stability, and lack of coloration over time.
成分(A)のアルキルエーテルカルボン酸又はその塩は、一般式(1)中、n=0、1、2、3、4の成分の質量割合が、R1の組成のうち最大含有量のアルキル鎖長成分において、(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 alkyl ether carboxylic acid of the component (A) or a salt thereof is an alkyl having the maximum content in the composition of R 1 in which the mass ratio of the components n = 0, 1, 2, 3, 4 is R 1. In the chain length 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 3.50: 0.89 to 3.00: 0.76 to 3.00: 0.63 to 1.6, foaming property, detergency, squeaky feeling during rinsing From the viewpoint of compatibility, it is preferable.
また、一般式(1)中、n=0の成分を9.9質量%以上12質量%未満含み、R1の組成のうち最大含有量のアルキル鎖長成分において、(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、R1の組成のうち最大含有量のアルキル鎖長成分において、(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)=1:0.99〜1.34:0.89〜1.40:0.76〜1.23:0.63〜1となるのが、泡質、泡量の観点から好ましい。 Further, in the general formula (1), the component of n = 0 include less than 9.9 wt% 12 wt%, in the alkyl chain length components of the maximum content of the composition of R 1, the (n = 0 component mass ): (Mass of n = 1 component): (mass of n = 2 component): (mass of n = 3 component): (mass of n = 4 component) = 1: 1.53-1.87: 1. 59 to 2.25: 1.33 to 2.16: 1.14 to 1.52, or 12 to 17% by mass of the n = 0 component, and the maximum among the compositions of R 1 In the alkyl chain length component of content, (mass of n = 0 component): (mass of n = 1 component): (mass of n = 2 component): (mass of n = 3 component): (n = 4 component) Mass) = 1: 0.99 to 1.34: 0.89 to 1.40: 0.76 to 1.23: 0.63 to 1 is preferable from the viewpoints of foam quality and foam amount.
さらに、一般式(1)中、n=0の成分を9.9〜11.5質量%含み、R1の組成のうち最大含有量のアルキル鎖長成分において、(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13〜15質量%含み、R1の組成のうち最大含有量のアルキル鎖長成分において、(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)=1:1.00〜1.31:0.93〜1.34:0.79〜1.18:0.63〜1となるのが、泡質、泡量の点から好ましい。 Further, in the general formula (1), the component of n = 0 contains 9.9 to 11.5% by mass, and in the alkyl chain length component of the maximum content in the composition of R 1 , (mass of n = 0 component) : (N = 1 component mass): (n = 2 component mass): (n = 3 component mass): (n = 4 component mass) = 1: 1.58-1.84: 1.72 To 2.17: 1.49 to 2.00: 1.14 to 1.52, or, in the general formula (1), the component of n = 0 is contained in an amount of 13 to 15% by mass, and the composition of R 1 In the maximum alkyl chain length component, (n = 0 component mass): (n = 1 component mass): (n = 2 component mass): (n = 3 component mass): (n = Mass of four components) = 1: 1.00 to 1.31: 0.93 to 1.34: 0.79 to 1.18: 0.63 to 1 in terms of foam quality and amount of foam To preferred.
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、nの付加モル数の平均値は、1.5〜10、さらには2.5〜6.4であり、n=0の成分を9.8〜27質量%、n=1の成分とn=2の成分を合計で27〜37質量%含有することが好ましい。また、式中、Mとしては、水素原子、ナトリウム、カリウム、アンモニウムが好ましい。このようにすることで、起泡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, and the average value of the number of added moles of n is 1.5 to 10, It is 2.5-6.4, It is preferable to contain 9.8-27 mass% of the component of n = 0, and 27-37 mass% of the component of n = 1 and the component of n = 2 in total. In the formula, M is preferably a hydrogen atom, sodium, potassium, or ammonium. In this way, foaming can be accelerated.
成分(A)において、一般式(1)中、R1は炭素数6〜20のアルキル基が好ましく、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の平均値は、2.5〜3.7であり、n=0の成分を9.8〜27質量%、n=1の成分とn=2の成分を合計で27〜37質量%含有することが好ましい。また、式中、Mとしては、水素原子、ナトリウム、カリウム、アンモニウムが好ましい。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 preferably 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 from 0 to 20, the average value of n is 2.5 to 3.7, and n = It is preferable to contain 9.8 to 27% by mass of 0 component and 27 to 37% by mass in total of n = 1 component and n = 2 component. In the formula, M is preferably a hydrogen atom, sodium, potassium, or ammonium. 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、nの平均値は、2.5〜3.4であり、n=0の成分を9.9〜27質量%、n=1の成分とn=2の成分を合計で27〜36.5質量%含有することが好ましい。また、式中、Mとしては、水素原子、ナトリウム、カリウム、アンモニウムが好ましい。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。本発明において、ストップフィーリングとは、洗浄剤組成物を適用して洗浄し、すすいだときの、すすぎ終わり時に手のひらが止まる感じのことをいう。 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, and the average value of n is 2.5 to 3.4. It is preferable to contain 9.9 to 27% by mass of 0 component and 27 to 36.5% by mass in total of n = 1 component and n = 2 component. In the formula, M is preferably a hydrogen atom, sodium, potassium, or ammonium. By doing in this way, the stop feeling property at the time of a rinse can be strengthened. In the present invention, the stop feeling refers to a feeling that the palm stops at the end of rinsing when the cleaning composition is applied and washed.
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、nの平均値は、2.8〜3.4であり、n=0の成分を9.9〜16質量%、n=1の成分とn=2の成分を合計で27〜36.5質量%含むものが好ましい。また、式中、Mとしては、水素原子、ナトリウム、カリウム、アンモニウムが好ましい。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 of n is 2.8 to 3.4, and n = 0 Is preferably 9.9 to 16% by mass and contains 27 to 36.5% by mass in total of n = 1 and n = 2. In the formula, M is preferably a hydrogen atom, sodium, potassium, or ammonium. 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70〜95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%、n=1の成分とn=2の成分を合計で35〜36.1質量%含むものが好ましい。また、式中、Mとしては、水素原子、ナトリウム、カリウム、アンモニウムが好ましい。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 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 70 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 Is preferably 9.9 to 15% by mass and contains 35 to 36.1% by mass in total of n = 1 and n = 2. In the formula, M is preferably a hydrogen atom, sodium, potassium, or ammonium. By doing in this way, foam amount and foam quality 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 the 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の成分の合計量〕
R1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の成分の合計量を算出した。
[Component amount of n = 0, total amount 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 set to 100%, and the total amount of n = 0, n = 1 and n = 2 was calculated.
〔nの平均付加モル数〕
R1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質量割合に関しては、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 mass 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 composition of R 1 The alkyl chain length component was identified from the area ratio of n = 0, n = 1, n = 2, n = 3, and n = 4 of the maximum component.
成分(A)のアルキルエーテルカルボン酸又はその塩は、前記のような組成を有するもので、含有量は、泡立ち、泡の厚み感、すすぎ時のなめらかさ、すすぎ時のストップフィーリング、及びタオルドライ後のしっとり感を向上させる観点から、全組成中に酸として1質量%以上であり、2質量%以上が好ましく、3質量%以上がより好ましく、8質量%以下であり、5質量%以下が好ましく、4質量%以下がより好ましい。また、成分(A)の含有量は、全組成中に酸として1〜8質量%であり、2〜5質量%が好ましく、3〜4質量%がより好ましい。 The component (A) alkyl ether carboxylic acid or salt thereof has the composition as described above, and the content is foaming, foam thickness, smoothness when rinsing, stop feeling when rinsing, and towel From the viewpoint of improving moist feeling after drying, the acid content in the entire composition is 1% by mass or more, preferably 2% by mass or more, more preferably 3% by mass or more, and 8% by mass or less, and 5% by mass or less. Is preferable, and 4 mass% or less is more preferable. Moreover, content of a component (A) is 1-8 mass% as an acid in the whole composition, 2-5 mass% is preferable, and 3-4 mass% is more preferable.
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、泡立ちの早さ、泡のとろみ感を向上させる観点から、その炭素数11〜17のアルキル基又はアルケニル基が好ましく、炭素数11〜15のアルキル基がより好ましい。
より具体的には、例えば、ラウリン酸、ミリスチン酸、パルミチン酸、ステアリン酸、イソステアリン酸、オレイン酸、アラキン酸、ベヘニン酸等が挙げられる。
また、R2は少なくとも炭素数11のアルキル基を含み、R2の平均炭素数は11〜15であり、泡立ちの早さを向上させる観点から、11〜13が好ましく、11.5〜12.5がより好ましく、11.5〜12がさらにより好ましい。
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, and from the viewpoint of improving the speed of foaming and the feeling of foam thickening, the alkyl group or alkenyl group having 11 to 17 carbon atoms is preferable. An alkyl group having 11 to 15 carbon atoms is more preferable.
More specifically, for example, lauric acid, myristic acid, palmitic acid, stearic acid, isostearic acid, oleic acid, arachidic acid, behenic acid and the like can be mentioned.
Further, R 2 comprises at least an alkyl group having a carbon number of 11, the average number of carbon atoms in R 2 is 11 to 15, from the viewpoint of improving the fast foaming, 11-13 preferably, from 11.5 to 12. 5 is more preferable, and 11.5 to 12 is even more preferable.
さらに、皮膚洗浄剤組成物中の全脂肪酸に対する、炭素数11のアルキル基を有する脂肪酸の質量割合(炭素数11のアルキル基を有する脂肪酸/全脂肪酸)は、泡立ちの早さ及び泡の厚み感を向上させる観点から、0.5〜1であり、0.50〜0.80が好ましく、0.55〜0.60がより好ましい。
また、炭素数11のアルキル基を有する脂肪酸以外の脂肪酸に対する炭素数11のアルキル基を有する脂肪酸の質量割合(炭素数11のアルキル基を有する脂肪酸/炭素数11のアルキル基を有する脂肪酸以外の脂肪酸)は、泡の厚み感及び泡のとろみ感を向上させる観点から、0.4〜0.9が好ましく、0.45〜0.8がより好ましく、0.48〜0.7がさらに好ましく、0.5〜0.65がさらにより好ましい。
Furthermore, the mass ratio of the fatty acid having an alkyl group having 11 carbon atoms to the total fatty acid in the skin cleansing composition (fatty acid having 11 alkyl groups / total fatty acid) is the speed of foaming and the feeling of foam thickness. From the viewpoint of improving the ratio, it is 0.5 to 1, preferably 0.50 to 0.80, and more preferably 0.55 to 0.60.
The mass ratio of fatty acids having 11 alkyl groups to fatty acids other than fatty acids having 11 alkyl groups (fatty acids other than fatty acids having 11 alkyl groups / fatty acids having 11 alkyl groups). ) Is preferably from 0.4 to 0.9, more preferably from 0.45 to 0.8, and even more preferably from 0.48 to 0.7, from the viewpoint of improving the thickness feeling of the foam and the thick feeling of the foam. 0.5 to 0.65 is even more preferable.
成分(B)の脂肪酸は、前記のような組成を有するもので、その含有量は、泡立ち、泡の厚み感、及び泡立ちの早さを向上させる観点から、全組成中に8〜16質量%であり、10〜15質量%が好ましく、13.5〜14.5質量%がより好ましい。 The fatty acid of component (B) has the composition as described above, and its content is 8 to 16% by mass in the total composition from the viewpoint of improving foaming, foam thickness feeling, and speed of foaming. 10 to 15% by mass is preferable, and 13.5 to 14.5% by mass is more preferable.
本発明で用いる成分(C)の両性界面活性剤は、通常の洗浄剤に用いられるものであれば制限されず、例えば、ラウリルジメチルアミノ酢酸ベタイン等の酢酸ベタイン型界面活性剤、ラウリルジメチルアミンオキサイド等のアミンオキサイド型界面活性剤、2−アルキル−N−カルボキシメチル−N−ヒドロキシエチルイミダゾリニウムベタイン等のイミダゾリニウムベタイン型界面活性剤、ラウリン酸アミドプロピルベタイン等のアミドベタイン型界面活性剤、ラウリルヒドロキシスルホベタイン等のスルホベタイン型界面活性剤などが挙げられる。
これらのうち、泡立ちの早さ及び洗浄剤組成物の使用感を向上させる観点から、ラウリン酸アミドプロピルベタイン等のアミドベタイン型界面活性剤、ラウリルヒドロキシスルホベタイン等のスルホベタイン型界面活性剤が好ましい。
The amphoteric surfactant of the component (C) used in the present invention is not limited as long as it is used in ordinary detergents. For example, betaine acetate type surfactants such as lauryldimethylaminoacetic acid betaine, lauryldimethylamine oxide Amine oxide type surfactants such as 2-alkyl-N-carboxymethyl-N-hydroxyethylimidazolinium betaine and the like, and amide betaine type surfactants such as lauric acid amidopropyl betaine And sulfobetaine-type surfactants such as laurylhydroxysulfobetaine.
Of these, amide betaine surfactants such as lauric acid amidopropyl betaine and sulfobetaine surfactants such as lauryl hydroxysulfobetaine are preferable from the viewpoint of improving the speed of foaming and the usability of the detergent composition. .
成分(C)の両性界面活性剤は、1種又は2種以上を用いることができ、その含有量は、泡立ちの早さを向上させる観点から、全組成中に0.5〜7質量%であり、1〜5質量%が好ましく、2〜4質量%がより好ましい。 One or more amphoteric surfactants of component (C) can be used, and the content thereof is 0.5 to 7% by mass in the total composition from the viewpoint of improving the speed of foaming. Yes, 1-5 mass% is preferable, and 2-4 mass% is more preferable.
本発明の皮膚洗浄剤組成物は、成分(D)として、(D1)電荷密度が0.5〜4.5meq/gのカチオン化ポリマー、(D2)ノニオン性のガム類、及び(D3)ヒドロキシエチル基又はヒドロキシプロピル基が付加したノニオン性セルロースの3種のポリマーを含有することにより、とろみ感ある泡を得ることができ、また、厚み感のある泡を得ることができる。 The skin cleansing composition of the present invention comprises, as component (D), (D1) a cationized polymer having a charge density of 0.5 to 4.5 meq / g, (D2) nonionic gums, and (D3) hydroxy By containing three types of nonionic cellulose polymers to which an ethyl group or a hydroxypropyl group is added, foam with a thick feeling can be obtained, and a foam with a thick feeling can be obtained.
成分(D1)のカチオン化ポリマーは、電荷密度が0.5〜4.5meq/gであり、泡のとろみ感を向上させる観点から、4.1〜4.3meq/gが好ましい。ここで、カチオン化ポリマーの電荷密度は、ポリマー1g当たりのカチオン性基モル数×1000(meq/g)である。
また、成分(D1)のカチオン化ポリマーは、泡のとろみ感及び洗浄剤組成物の使用感を向上させる観点から、重量平均分子量は、8万〜150万が好ましく、9万〜100万がより好ましく、9.5万から50万がさらに好ましく、10万〜20万がさらにより好ましい。
The cationized polymer of the component (D1) has a charge density of 0.5 to 4.5 meq / g, and is preferably 4.1 to 4.3 meq / g from the viewpoint of improving the foaming feeling. Here, the charge density of the cationized polymer is the number of moles of cationic groups per gram of polymer × 1000 (meq / g).
The weight average molecular weight of the cationized polymer of the component (D1) is preferably 80,000 to 1,500,000, more preferably 90,000 to 1,000,000, from the viewpoint of improving the foamy feeling and the feeling of use of the cleaning composition. Preferably, 95,000 to 500,000 are more preferable, and 100,000 to 200,000 are even more preferable.
成分(D1)のカチオン化ポリマーとしては、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、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等が挙げられる。中でも、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が好ましい。 Examples of the cationized polymer of component (D1) include cationized cellulose, cationized starch, cationized guar gum, cationized tara gum, cationized locust bean gum, cationized fenugreek gum, diallyldialkyl quaternary ammonium salt / acrylamide copolymer. Products, diallyldialkyl quaternary ammonium salts / acrylamide / acrylic acid copolymers, and the like. Of these, diallyldialkyl quaternary ammonium salt / acrylamide copolymer is preferable.
より具体的には、ジアリルジアルキル四級アンモニウム塩(DMDAAC)/アクリルアミド(AM)共重合物として、マーコート550(重量平均分子量:16万、カチオン電荷密度:4.22meq/g、DMDAAC:AM=50:50)、マーコート2200(重量平均分子量:9万、カチオン電荷密度:4.22meq/g、DMDAAC:AM=50:50)、マーコートS(重量平均分子量:26万、カチオン電荷密度:4.22meq/g、DMDAAC:AM=50:50)[以上、NALCO社、アクリルアミドとジアリルジメチルアンモニウム塩の共重合体]、ポイズC−60H(重量平均分子量:60万、カチオン電荷密度:1.07〜1.78meq/g)、カチセロM−80(重量平均分子量:80万、カチオン電荷密度:0.93〜1.21meq/g)、ポイズC−150L(重量平均分子量:150万、カチオン電荷密度:0.71〜1.07meq/g)[以上、花王社、カチオン化セルロース(塩化O−[2−ヒドロキシ−3−(トリメチルアンモニオ)プロピル]ヒドロキシエチルセルロース)]、ジャガーC17(重量平均分子量:30万、カチオン電荷密度:1.07〜1.50meq/g)、ジャガーC14(重量平均分子量:30万、カチオン電荷密度:0.93〜1.21meq/g)[以上、ローディア社、カチオン化グアーガム(グアーヒドロキシプロピルトリアンモニウムクロリド)]等が挙げられる。
なお、カチオン化セルロースとグアーヒドロキシプロピルトリアンモニウムクロリドのカチオン化電荷密度は、高分子中に含まれる窒素が100%カチオン化されていると仮定し、ポリマー中の窒素含有量比率(質量%)から求めた。
More specifically, as a diallyldialkyl quaternary ammonium salt (DMDAAC) / acrylamide (AM) copolymer, Marquat 550 (weight average molecular weight: 160,000, cationic charge density: 4.22 meq / g, DMDAAC: AM = 50 : 50), Marquat 2200 (weight average molecular weight: 90,000, cationic charge density: 4.22 meq / g, DMDAAC: AM = 50: 50), Marquat S (weight average molecular weight: 260,000, cationic charge density: 4.22 meq) / G, DMDAAC: AM = 50: 50) [Nole, NALCO, copolymer of acrylamide and diallyldimethylammonium salt], Poise C-60H (weight average molecular weight: 600,000, cationic charge density: 1.07 to 1) .78 meq / g), Katachiro M-80 (weight average molecular weight: 800,000, cationic charge density: 0.93 .21 meq / g), Poise C-150L (weight average molecular weight: 1,500,000, cationic charge density: 0.71-1.07 meq / g) [above, Kao Corporation, cationized cellulose (O- [2-hydroxy-chloride] 3- (trimethylammonio) propyl] hydroxyethylcellulose)], Jaguar C17 (weight average molecular weight: 300,000, cationic charge density: 1.07-1.50 meq / g), Jaguar C14 (weight average molecular weight: 300,000, cation Charge density: 0.93 to 1.21 meq / g) [above, Rhodia, cationized guar gum (guar hydroxypropyltriammonium chloride)] and the like.
The cationized charge density of cationized cellulose and guar hydroxypropyltriammonium chloride is based on the nitrogen content ratio (% by mass) in the polymer, assuming that the nitrogen contained in the polymer is 100% cationized. Asked.
成分(D1)は、1種又は2種以上を用いることができ、泡のとろみ感及びすすぎ時のストップフィーリングの両立性を向上させる観点から、その含有量は、全組成中に0.1〜1.5質量%が好ましく、0.3〜1.0質量%がより好ましく、0.5〜0.8質量%が更に好ましい。 Component (D1) can be used singly or in combination of two or more. From the viewpoint of improving the consistency of foam and the feeling of stop feeling at the time of rinsing, the content is 0.1% in the total composition. -1.5 mass% is preferable, 0.3-1.0 mass% is more preferable, 0.5-0.8 mass% is still more preferable.
成分(D2)のノニオン性のガム類としては、例えば、グアガム、キサンタンガム、ジェランガム、カラギーナン、ローストビーンガム、タラガム、これらの誘導体などが挙げられる。
これらのうち、泡のとろみ感及び泡の厚み感を向上させる観点から、グアガム、キサンタンガムが好ましい。
Examples of the nonionic gums of component (D2) include guar gum, xanthan gum, gellan gum, carrageenan, roast bean gum, tara gum, and derivatives thereof.
Of these, guar gum and xanthan gum are preferable from the viewpoint of improving the foam thickness and foam thickness.
成分(D2)は、1種又は2種以上を用いることができ、泡のとろみ感及び泡の厚み感を向上させる観点から、含有量は、全組成中に0.05〜0.5質量%が好ましく、0.1〜0.3質量%がより好ましく、0.1〜0.2質量%が更に好ましい。 Component (D2) can be used alone or in combination of two or more, and the content is 0.05 to 0.5% by mass in the total composition from the viewpoint of improving the foam thickness and foam thickness. Is preferable, 0.1-0.3 mass% is more preferable, 0.1-0.2 mass% is still more preferable.
本発明で用いる成分(D3)のセルロースは、ヒドロキシエチル基又はヒドロキシプロピル基が付加したものである。すなわち、セルロースの水酸基における水素原子の一部がヒドロキシエチル基又はヒドロキシプロピル基で置換されているものであり、これら以外の置換基を有していても良い。 The component (D3) cellulose used in the present invention has a hydroxyethyl group or a hydroxypropyl group added thereto. That is, a part of hydrogen atoms in the hydroxyl group of cellulose is substituted with a hydroxyethyl group or a hydroxypropyl group, and may have a substituent other than these.
具体的には、ヒドロキシエチルセルロース、ヒドロキシプロピルセルロース、ヒドロキシエチルメチルセルロース、ヒドロキシプロピルメチルセルロース等が挙げられる。
これらは、セルロースに苛性ソーダを反応させてアルカリセルロースとし、次いで、塩化メチル、モノクロル酢酸、エチレンオキサイド、プロピレンオキサイド等を作用させ、セルロースの水酸基における水素原子を置換して得られるものである。
Specific examples include hydroxyethyl cellulose, hydroxypropyl cellulose, hydroxyethyl methyl cellulose, hydroxypropyl methyl cellulose, and the like.
These are obtained by reacting cellulose with caustic soda to make alkaline cellulose, and then reacting methyl chloride, monochloroacetic acid, ethylene oxide, propylene oxide, etc. to replace the hydrogen atom in the hydroxyl group of cellulose.
成分(D3)のセルロースは、泡の持続性を向上させる観点から、平均置換度は0より大きいのが好ましく、0.5以上がより好ましく、3以下が好ましく、2以下がより好ましい。また、平均分子量は、洗浄剤組成物への溶解性及び泡の持続性を向上させる観点から、200,000以上が好ましく、500,000以上がより好ましく、650,000以上がより好ましく、3,000,000以下が好ましく、2,000,000以下がより好ましく、1,600,000以下が更に好ましい。
なお、本発明において、平均置換度は、NMRにより求められ、平均分子量は、標準物質をポリエチレンオキシドとしてゲルパーミエーションクロマトグラフィー(GPC)−多角度レーザー光散乱検出装置(MALLS)システムを用いることにより測定される。
From the viewpoint of improving the sustainability of foam, the component (D3) cellulose preferably has an average degree of substitution of greater than 0, more preferably 0.5 or more, preferably 3 or less, and more preferably 2 or less. The average molecular weight is preferably 200,000 or more, more preferably 500,000 or more, more preferably 650,000 or more, from the viewpoint of improving the solubility in the cleaning composition and the persistence of the foam, 000,000 or less is preferable, 2,000,000 or less is more preferable, and 1,600,000 or less is more preferable.
In the present invention, the average degree of substitution is determined by NMR, and the average molecular weight is determined by using a gel permeation chromatography (GPC) -multi-angle laser light scattering detector (MALLS) system with polyethylene oxide as a standard substance. Measured.
成分(D3)としては、ヒドロキシエチルセルロース、ヒドロキシプロピルメチルセルロースが好ましく、平均置換度が0.5〜2、平均分子量が650,000〜1,600,000のものが好ましい。 Component (D3) is preferably hydroxyethyl cellulose or hydroxypropyl methylcellulose, preferably having an average degree of substitution of 0.5 to 2 and an average molecular weight of 650,000 to 1,600,000.
また、成分(D3)としては、例えば、ヒドロキシエチルセルロースでは、CELLOSIZE QP52000H(ダウ・ケミカル社製)、HECダイセル SE400、SE500、SE600、SE850、SE900(以上、ダイセルファインケム社製)等;ヒドロキシプロピルメチルセルロースでは、METOLOSE 60SH、65SH、90SH(以上、信越化学工業社製)、BENECEL E50、E4M、E10M、F4MC、K99C、K4M、K15M、K35M、K100M、K200M(以上、ASHLAND社製)等の市販品を使用することができる。 As the component (D3), for example, for hydroxyethyl cellulose, CELLOSIZE QP52000H (manufactured by Dow Chemical), HEC Daicel SE400, SE500, SE600, SE850, SE900 (above, Daicel Finechem), etc .; , METALOSE 60SH, 65SH, 90SH (above, manufactured by Shin-Etsu Chemical Co., Ltd.), BENECEL E50, E4M, E10M, F4MC, K99C, K4M, K15M, K35M, K100M, K200M (above, made by ASHLAND) etc. can do.
成分(D3)は、1種又は2種以上を用いることができ、泡の持続性及び使用性(洗浄道具への液の取りやすさ)を向上させる観点から、その含有量は、全組成中に0.1〜1質量%が好ましく、0.2〜0.8質量%がより好ましく、0.2〜0.5質量%が更に好ましい。 Component (D3) can be used singly or in combination of two or more, and from the viewpoint of improving the durability and usability of the foam (ease of taking the liquid into the cleaning tool), its content is in the total composition 0.1 to 1% by mass is preferable, 0.2 to 0.8% by mass is more preferable, and 0.2 to 0.5% by mass is still more preferable.
本発明において、成分(D2)及び(D3)の合計含有量は、泡立ちの早さ及び泡の持続性を向上させ、並びにすすぎ時の残留感を低減させる観点から、全組成中に0.1〜0.8質量%が好ましく、0.2〜0.6質量%がより好ましく、0.3〜0.4質量%が更に好ましい。 In the present invention, the total content of components (D2) and (D3) is 0.1% in the total composition from the viewpoint of improving the speed of foaming and foam persistence, and reducing the residual feeling during rinsing. -0.8 mass% is preferable, 0.2-0.6 mass% is more preferable, 0.3-0.4 mass% is still more preferable.
また、本発明において、成分(D2)及び(D3)の質量割合(D2)/(D3)は、泡立ちの早さ及び泡の厚み感を向上させる観点から、0.1〜3が好ましく、0.2〜2.5がより好ましく、0.3〜0.5が更に好ましい。 In the present invention, the mass ratio (D2) / (D3) of the components (D2) and (D3) is preferably 0.1 to 3 from the viewpoint of improving the speed of foaming and the feeling of foam thickness. 2 to 2.5 is more preferable, and 0.3 to 0.5 is still more preferable.
本発明において、成分(D2)及び(D3)の含有量に対する、成分(D1)の質量割合(D1)/((D2)+(D3))は、泡のとろみ感及びすすぎ時のなめらかさを向上させる観点から、0.2〜2.5が好ましく、0.25〜2がより好ましく、1.5〜2が更に好ましい。 In the present invention, the mass ratio (D1) / ((D2) + (D3)) of the component (D1) with respect to the contents of the components (D2) and (D3) indicates the thickness of the foam and the smoothness during rinsing. From a viewpoint of improving, 0.2-2.5 are preferable, 0.25-2 are more preferable, and 1.5-2 are still more preferable.
また、本発明において、成分(D1)、(D2)及び(D3)の合計含有量は、泡のとろみ感、すすぎ時のなめらかさ及びすすぎ終了時の残留感のなさを向上させる観点から、全組成中に0.5〜1.6質量%が好ましく、0.7〜1.4質量%がより好ましく、1.0〜1.2質量%が更に好ましい。 Further, in the present invention, the total content of the components (D1), (D2) and (D3) is all from the viewpoint of improving the foam thickness, smoothness at the time of rinsing and lack of residual feeling at the end of rinsing. 0.5-1.6 mass% is preferable in a composition, 0.7-1.4 mass% is more preferable, 1.0-1.2 mass% is still more preferable.
本発明において、水は溶媒として用いられ、その含有量は、全組成中に45質量%以上が好ましく、55質量%以上がより好ましく、85質量%以下が好ましく、75質量%以下がより好ましい。 In the present invention, water is used as a solvent, and the content thereof is preferably 45% by mass or more, more preferably 55% by mass or more, preferably 85% by mass or less, and more preferably 75% by mass or less in the total composition.
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)、(C)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、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 (C), moisturizers, oily components, bactericides, anti-inflammatory agents, Preservatives, chelating agents, thickeners, salts, pearling agents, scrub agents, fragrances, cooling agents, pigments, ultraviolet absorbers, antioxidants, plant extracts and the like can be contained.
本発明の皮膚洗浄剤組成物を起泡させることによりできる泡は、皮膚上にゆっくり拡げると泡が動きやすく、すばやく拡げた時には、泡のボリューム感が増し、泡が動きにくくなるものであり、泡の抵抗が高まるために、すばやく泡を拡げた時においても、泡を皮膚で実感できる(泡の存在感が高まる)という特異な性質を示す。この特徴により、よりとろみのある、なめらかな泡で全身を洗浄することができ、うるおいのあるなめらかな肌で、やわらかい肌を実感することができるものである。
さらに、後述の試験例1で示される泡粘度変化が0mPa・s以上である泡は、より弾力性があり、厚み感のある泡となるため、洗浄中にわたって、すべりが良くとろみのあるなめらかな泡で全身を洗浄することができ、洗浄後にはうるおいのあるなめらかな肌で、やわらかい肌を強く実感することができるものである。
泡粘度変化は、より弾力性があり、厚み感のある泡を得る観点から、0以上であることが好ましく、0〜100mPa・sがより好ましく、5〜80mPa・sがさらに好ましく、10〜70mPa・sがよりさらに好ましく、20〜65mPa・sがさらに好ましく、30〜60mPa・sが特に好ましい。
The foam produced by foaming the skin cleansing composition of the present invention is easy to move when expanded slowly on the skin, and when expanded quickly, the volume of the foam increases and the foam becomes difficult to move, Since the resistance of the foam is increased, even when the foam is quickly expanded, the foam can be felt on the skin (the presence of the foam is increased). With this feature, the whole body can be washed with a thicker and smoother foam, and a soft skin can be realized with a moist and smooth skin.
Furthermore, since the foam having a foam viscosity change of 0 mPa · s or more shown in Test Example 1 described later is more elastic and thick, it is smooth and smooth during the cleaning. The whole body can be washed with foam, and after washing, the skin is moist and smooth, and the soft skin can be strongly felt.
The change in foam viscosity is preferably 0 or more, more preferably 0 to 100 mPa · s, further preferably 5 to 80 mPa · s, and more preferably 10 to 70 mPa from the viewpoint of obtaining a more elastic and thick foam. · S is more preferable, 20 to 65 mPa · s is more preferable, and 30 to 60 mPa · s is particularly preferable.
また、本発明の皮膚洗浄剤組成物は、同様の観点から、ジプロピレングリコール、1,3−ブチレングリコール、グリセリン、プロピレングリコール、ソルビトール、マルビトール、ジグリセリン、ラフィノース、ヘキシレングリコール等の多価アルコールを含有することが好ましく、グリセリン、プロピレングリコールから選ばれる少なくともいずれか1種を含有することがより好ましい。 In addition, the skin cleansing composition of the present invention is a polyhydric alcohol such as dipropylene glycol, 1,3-butylene glycol, glycerin, propylene glycol, sorbitol, malbitol, diglycerin, raffinose, hexylene glycol and the like from the same viewpoint. Is preferable, and it is more preferable to contain at least one selected from glycerin and propylene glycol.
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(VISCOMETER TVB-10、東機産業社製、No.3ローター又はNo.4ローター、30、12又は6rpm、60秒後、30℃の条件)で測定したときの粘度が200〜80000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であるのが好ましく、pH5〜10.5がより好ましく、pH5〜10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 resulting cleaning composition may be either liquid or solid, but when it is liquid, it is a B-type viscometer (VISCOMETER TVB-10, manufactured by Toki Sangyo Co., Ltd., No. 3 rotor or No. (4 rotor, 30, 12 or 6 rpm, 60 seconds later, 30 ° C.), the viscosity is preferably 200 to 80000, and can be adjusted by appropriately selecting the blending components.
Moreover, it is preferable that pH is 3-12, pH 5-10.5 is more preferable, and pH 5-10 is still more preferable. In addition, the measurement of pH is a value obtained by diluting each cleaning composition 20 times with 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、ボディーソープがより好ましい。
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、タオル、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、更に以下の組成物を開示する。
The skin cleansing composition of the present invention is suitable as, for example, a facial cleanser, a body soap, a hand soap, etc., and a body soap is more preferable.
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. In addition, an appropriate amount can be applied to cleaning aids such as towels, sponges, brushes, etc., and foamed for cleaning.
This invention discloses the following compositions further regarding embodiment mentioned above.
<1>次の成分(A)、(B)、(C)及び(D):
(A)一般式(1)
<1> The following components (A), (B), (C) and (D):
(A) General formula (1)
(式中、R1は炭素数4〜22のアルキル基を示し、nは0〜20の数を示し、Mは水素原子、アルカリ金属、アルカリ土類金属、アンモニウム又は有機アンモニウムを示す)
で表されるアルキルエーテルカルボン酸又はその塩であって、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の成分を合計で40質量%未満含むアルキルエーテルカルボン酸又はその塩 1〜8質量%、
(B)一般式(2)
(In the formula, R 1 represents an alkyl group having 4 to 22 carbon atoms, n represents a number of 0 to 20, and M represents a hydrogen atom, an alkali metal, an alkaline earth metal, ammonium, or organic ammonium).
Wherein R 1 has an average carbon number of 10.8 to 12.8, contains 4.3 to 30% by mass of n = 0, and n = 1 An alkyl ether carboxylic acid or a salt thereof containing 1 to 8% by mass,
(B) General formula (2)
(式中、R2は炭素数9〜21のアルキル基又はアルケニル基を示し、R2は少なくとも炭素数11のアルキル基を含み、R2の平均炭素数は11〜16である)
で表される脂肪酸 10〜14質量%、
(C)両性界面活性剤 0.5〜5質量%、
(D1)電荷密度が0.5〜4.5meq/gのカチオン化ポリマー、
(D2)ノニオン性のガム類、
(D3)ヒドロキシエチル基又はヒドロキシプロピル基が付加したノニオン性セルロース
を含有し、全脂肪酸に対する炭素数12のアルキル基を有する脂肪酸の質量割合(炭素数12のアルキル基を有する脂肪酸/全脂肪酸)が、0.5〜1である皮膚洗浄剤組成物。
(Wherein R 2 represents an alkyl group or alkenyl group having 9 to 21 carbon atoms, R 2 includes at least an alkyl group having 11 carbon atoms, and R 2 has an average carbon number of 11 to 16)
10 to 14% by mass of a fatty acid represented by
(C) Amphoteric surfactant 0.5-5% by mass,
(D1) a cationized polymer having a charge density of 0.5 to 4.5 meq / g,
(D2) nonionic gums,
(D3) Nonionic cellulose to which hydroxyethyl group or hydroxypropyl group is added, and the mass ratio of fatty acids having 12 alkyl groups to all fatty acids (fatty acids having 12 alkyl groups / total fatty acids) The skin cleansing composition which is 0.5-1.
<2>成分(A)において、一般式(1)中、好ましくは、R1は炭素数6〜20のアルキル基であって、炭素数8〜18のアルキル基がより好ましく、炭素数8〜16のアルキル基がさらに好ましく、炭素数10〜16のアルキル基がよりさらに好ましい前記<1>機足の皮膚洗浄剤組成物。
<3>成分(A)において、一般式(1)中、好ましくは、R1の平均炭素数が10.8〜12.5であって、12.1〜12.4がより好ましい前記<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、好ましくは、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%未満であるのがより好ましく、60〜95質量%がさらに好ましく、70〜95質量%であるのがよりさらに好ましい前記<1>〜<3>のいずれか1記載の皮膚洗浄剤組成物。
<5>成分(A)において、一般式(1)中、好ましくは、nの平均値(エチレンオシキシドの平均付加モル数)が、1.5〜10であって、2.5〜6.4がより好ましく、2.5〜3.7がさらに好ましく、2.5〜3.4がよりさらに好ましく、2.8〜3.4がさらに好ましく、2.8〜3.1がよりさらに好ましい前記<1>〜<4>のいずれか1記載の皮膚洗浄剤組成物。
<2> In the component (A), in the general formula (1), R 1 is preferably an alkyl group having 6 to 20 carbon atoms, more preferably an alkyl group having 8 to 18 carbon atoms, and 8 to 8 carbon atoms. The <1> foot-and-skin skin cleansing composition is more preferably an alkyl group having 16 alkyl groups, and still more preferably an alkyl group having 10 to 16 carbon atoms.
<3> In the component (A), in the general formula (1), preferably, R 1 has an average carbon number of 10.8 to 12.5, and more preferably 12.1 to 12.4. > Or <2>.
<4> In component (A), in general formula (1), preferably, R 1 contains two or more alkyl groups, and the component having the largest alkyl chain length is 55% by mass or more and 97% by mass. The skin cleanser composition according to any one of <1> to <3>, more preferably less than%, more preferably from 60 to 95% by mass, and even more preferably from 70 to 95% by mass.
<5> In the component (A), in the general formula (1), preferably, the average value of n (average added mole number of ethylene oxide) is 1.5 to 10, and 2.5 to 6. 4 is more preferable, 2.5 to 3.7 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 still more preferable The skin cleansing composition according to any one of <1> to <4>.
<6>成分(A)において、一般式(1)中、n=0の成分を、好ましくは4.9〜27質量%、より好ましくは9.6〜27質量%、さらに好ましくは、9.6質量%を超え27質量%以下、また、好ましくは9.8〜27質量%、より好ましくは9.9〜27質量%、更に好ましくは9.9〜16質量%、より好ましくは9.9〜15質量%含む前記<1>〜<5>のいずれか1記載の皮膚洗浄剤組成物。
<7>成分(A)において、一般式(1)中、n=1の成分とn=2の成分を合計で、好ましくは21質量%以上40質量%未満、より好ましくは27〜37質量%、さらに好ましくは27〜36.5質量%、さらにより好ましくは35〜36.1質量%含む前記<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、好ましくは、n=0、1、2、3、4の成分の質量割合が、R1の組成のうち最大含有量のアルキル鎖長成分において、(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である前記<1>〜<7>のいずれか1記載の皮膚洗浄剤組成物。
In <6> component (A), the component of n = 0 in general formula (1) becomes like this. Preferably it is 4.9-27 mass%, More preferably, it is 9.6-27 mass%, More preferably, 9. More than 6 mass% and 27 mass% or less, preferably 9.8-27 mass%, more preferably 9.9-27 mass%, still more preferably 9.9-16 mass%, more preferably 9.9. The skin cleanser composition according to any one of <1> to <5>, which is contained in 15% by mass.
In <7> component (A), in general formula (1), the component of n = 1 and the component of n = 2 are total, Preferably they are 21 mass% or more and less than 40 mass%, More preferably, it is 27-37 mass%. The skin cleanser composition according to any one of <1> to <6>, further preferably 27 to 36.5% by mass, and even more preferably 35 to 36.1% by mass.
<8> In the component (A), in the general formula (1), preferably, the mass ratio of the components of n = 0, 1, 2, 3, 4 is the maximum alkyl chain length in the composition of R 1 In the components, (n = 0 component mass): (n = 1 component mass): (n = 2 component mass): (n = 3 component mass): (n = 4 component mass) = 1 The skin cleansing agent according to any one of <1> to <7>, which is 0.99 to 3.50: 0.89 to 3.00: 0.76 to 3.00: 0.63 to 1.6. Composition.
<9>成分(A)の含有量が、好ましくは、全組成中に酸として2質量%以上であって、3質量%以上がより好ましく、5質量%以下が好ましく、4質量%以下がより好ましい前記<1>〜<8>のいずれか1記載の皮膚洗浄剤組成物。
<10>成分(B)の脂肪酸が、一般式(2)において、好ましくは、R2が炭素数11〜17のアルキル基又はアルケニル基であって、炭素数11〜15のアルキル基がより好ましい前記<1>〜<9>のいずれか1記載の皮膚洗浄剤組成物。
<11>成分(B)の脂肪酸が、一般式(2)において、好ましくは、R2の平均炭素数が11〜13であって、11.5〜12.5がより好ましく、11.5〜12がさらにより好ましい前記<1>〜<10>のいずれか1記載の皮膚洗浄剤組成物。
<12>全脂肪酸に対する炭素数11のアルキル基を有する脂肪酸の質量割合(炭素数11のアルキル基を有する脂肪酸/全脂肪酸)は、好ましくは、0.55以上であって、0.80以下が好ましく、0.60以下がより好ましい前記<1>〜<11>のいずれか1記載の皮膚洗浄剤組成物。
The content of <9> component (A) is preferably 2% by mass or more, more preferably 3% by mass or more, more preferably 5% by mass or less, and more preferably 4% by mass or less as the acid in the total composition. The skin cleansing composition according to any one of the above <1> to <8>.
<10> fatty acid component (B), in the general formula (2), preferably, in R 2 is an alkyl or alkenyl group of 11 to 17 carbon atoms, more preferably an alkyl group having 11 to 15 carbon atoms The skin cleansing composition according to any one of <1> to <9>.
In the general formula (2), the fatty acid of <11> component (B) is preferably an average carbon number of R 2 of 11 to 13, more preferably 11.5 to 12.5, and more preferably 11.5 to 12. The skin cleanser composition according to any one of <1> to <10>, wherein 12 is even more preferable.
<12> The mass ratio of the fatty acid having an alkyl group having 11 carbon atoms to the total fatty acid (fatty acid having an alkyl group having 11 carbon atoms / total fatty acid) is preferably 0.55 or more and 0.80 or less. The skin cleanser composition according to any one of <1> to <11>, preferably 0.60 or less.
<13>成分(B)の含有量が、好ましくは、全組成中に10質量%以上であって、13.5質量%以上がより好ましく、15質量%以下が好ましく、14.5質量%以下がより好ましい前記<1>〜<12>のいずれか1記載の皮膚洗浄剤組成物。
<14>成分(C)の両性界面活性剤が、好ましくは、アミドベタイン型界面活性剤、スルホベタイン型界面活性剤であって、ラウリン酸アミドプロピルベタイン、ラウリルヒドロキシスルホベタインがより好ましい前記<1>〜<13>のいずれか1記載の皮膚洗浄剤組成物。
<15>成分(C)の含有量が、好ましくは、全組成中に1質量%以上であって、2質量%以上がより好ましく、5質量%以下が好ましく、4質量%以下がより好ましい前記<1>〜<14>のいずれか1記載の皮膚洗浄剤組成物。
The content of <13> component (B) is preferably 10% by mass or more, more preferably 13.5% by mass or more, preferably 15% by mass or less, and preferably 14.5% by mass or less in the total composition. The skin cleansing composition according to any one of the above <1> to <12>, which is more preferable.
<14> The amphoteric surfactant of component (C) is preferably an amide betaine type surfactant or a sulfobetaine type surfactant, more preferably amide propyl betaine laurate or lauryl hydroxysulfo betaine <1 The skin cleanser composition according to any one of> to <13>.
The content of <15> component (C) is preferably 1% by mass or more in the total composition, more preferably 2% by mass or more, preferably 5% by mass or less, and more preferably 4% by mass or less. The skin cleansing composition according to any one of <1> to <14>.
<16>成分(D1)のカチオン化ポリマーが、好ましくは、電荷密度が4.1〜4.3meq/gである前記<1>〜<15>のいずれか1記載の皮膚洗浄剤組成物。
<17>成分(D1)のカチオン化ポリマーが、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、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であって、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がより好ましい前記<1>〜<16>のいずれか1記載の皮膚洗浄剤組成物。
<18>成分(D1)の含有量が、好ましくは、全組成中に0.1質量%以上であって、0.3質量%以上がより好ましく、0.5質量%以上が更に好ましく、1.5質量%以下が好ましく、1.0質量%以下がより好ましく、0.8質量%以下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。
<16> The skin cleanser composition according to any one of <1> to <15>, wherein the cationized polymer of component (D1) preferably has a charge density of 4.1 to 4.3 meq / g.
<17> The cationized polymer of component (D1) is preferably cationized cellulose, cationized starch, cationized guar gum, cationized cod gum, cationized locust bean gum, cationized fenugreek gum, diallyldialkyl quaternary ammonium salt / Any one of <1> to <16>, wherein the acrylamide copolymer is a diallyldialkyl quaternary ammonium salt / acrylamide / acrylic acid copolymer, and more preferably a diallyldialkyl quaternary ammonium salt / acrylamide copolymer. Skin cleansing composition.
The content of <18> component (D1) is preferably 0.1% by mass or more, more preferably 0.3% by mass or more, still more preferably 0.5% by mass or more, in the total composition. The skin cleanser composition according to any one of <1> to <17>, preferably 0.5% by mass or less, more preferably 1.0% by mass or less, and still more preferably 0.8% by mass or less.
<19>成分(D2)のノニオン性のガム類が、好ましくは、グアガム、キサンタンガム、ジェランガム、カラギーナン、ローストビーンガム、タラガム、これらの誘導体であって、グアガム、キサンタンガムがより好ましい前記<1>〜<18>のいずれか1記載の皮膚洗浄剤組成物。
<20>成分(D2)の含有量が、好ましくは、全組成中に0.05質量%以上であって、0.1質量%以上がより好ましく、0.5質量%以下が好ましく、0.3質量%以下がより好ましく、0.2質量%以下が更に好ましい前記<1>〜<19>のいずれか1記載の皮膚洗浄剤組成物。
<21>成分(D3)のノニオン性セルロースが、好ましくは、ヒドロキシエチルセルロース、ヒドロキシプロピルセルロース、ヒドロキシエチルメチルセルロース、ヒドロキシプロピルメチルセルロースである前記<1>〜<20>のいずれか1記載の皮膚洗浄剤組成物。
<22>成分(D3)の含有量が、好ましくは、全組成中に0.1質量%以上であって、0.2質量%以上がより好ましく、1質量%以下が好ましく、0.8質量%以下がより好ましく、0.5質量%以下が更に好ましい前記<1>〜<21>のいずれか1記載の皮膚洗浄剤組成物。
<19> The nonionic gums of component (D2) are preferably guar gum, xanthan gum, gellan gum, carrageenan, roast bean gum, tara gum, derivatives thereof, and more preferably guar gum and xanthan gum. <18> The skin cleanser composition according to any one of the above.
The content of the <20> component (D2) is preferably 0.05% by mass or more, more preferably 0.1% by mass or more, and preferably 0.5% by mass or less in the total composition. 3 mass% or less is more preferable, 0.2 mass% or less is still more preferable The skin cleaning composition in any one of said <1>-<19>.
<21> The skin cleanser composition according to any one of <1> to <20>, wherein the nonionic cellulose of component (D3) is preferably hydroxyethylcellulose, hydroxypropylcellulose, hydroxyethylmethylcellulose, or hydroxypropylmethylcellulose. object.
The content of <22> component (D3) is preferably 0.1% by mass or more, more preferably 0.2% by mass or more, and preferably 1% by mass or less, and 0.8% by mass in the total composition. % Or less is more preferable, and 0.5 mass% or less is still more preferable, The skin cleaning composition in any one of said <1>-<21>.
<23>成分(D2)及び(D3)の合計含有量が、好ましくは、全組成中に0.1質量%以上であって、0.2質量%以上がより好ましく、0.3質量%以上が更に好ましく、0.8質量%以下が好ましく、0.6質量%以下がより好ましく、0.4質量%以下が更に好ましい前記<1>〜<22>のいずれか1記載の皮膚洗浄剤組成物。
<24>成分(D2)及び(D3)の質量割合(D2)/(D3)が、好ましくは、0.1以上であって、0.2以上がより好ましく、0.3以上が更に好ましく、3以下が好ましく、2.5以下がより好ましく、0.5以下が更に好ましい前記<1>〜<23>のいずれか1記載の皮膚洗浄剤組成物。
<25>成分(D2)及び(D3)の含有量に対する、成分(D1)の質量割合(D1)/((D2)+(D3))が、好ましくは、0.2以上であって、0.25以上がより好ましく、1.5以上が更に好ましく、2.5以下が好ましく、2以下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。
The total content of <23> components (D2) and (D3) is preferably 0.1% by mass or more in the total composition, more preferably 0.2% by mass or more, and 0.3% by mass or more. Is more preferable, 0.8 mass% or less is preferable, 0.6 mass% or less is more preferable, 0.4 mass% or less is still more preferable, The skin cleaning composition in any one of said <1>-<22> object.
<24> The mass ratio (D2) / (D3) of the components (D2) and (D3) is preferably 0.1 or more, more preferably 0.2 or more, still more preferably 0.3 or more, 3 or less is preferable, 2.5 or less is more preferable, and 0.5 or less is still more preferable, The skin cleaning composition in any one of said <1>-<23>.
<25> The mass ratio (D1) / ((D2) + (D3)) of the component (D1) to the contents of the components (D2) and (D3) is preferably 0.2 or more and 0 The skin cleanser composition according to any one of <1> to <24>, wherein 25 or more is more preferable, 1.5 or more is more preferable, 2.5 or less is preferable, and 2 or less is more preferable.
<26>成分(D1)、(D2)及び(D3)の合計含有量が、好ましくは、全組成中に0.5質量%以上であって、0.7質量%以上がより好ましく、1.0質量%以上が更に好ましく、1.6質量%以下が好ましく、1.4質量%以下がより好ましく、1.2質量%以下が更に好ましい前記<1>〜<25>のいずれか1記載の皮膚洗浄剤組成物。
<27>水の含有量が、好ましくは、全組成中に45質量%以上であって、55質量%以上がより好ましく、85質量%以下が好ましく、75質量%以下がより好ましい前記<1>〜<26>のいずれか1記載の皮膚洗浄剤組成物。
<28>さらに、多価アルコールを含有するのが好ましく、ジプロピレングリコール、1,3−ブチレングリコール、グリセリン、プロピレングリコール、ソルビトール、マルビトール、ジグリセリン、ラフィノース、ヘキシレングリコールがより好ましく、グリセリン、プロピレングリコールがさらに好ましい前記<1>〜<27>のいずれか1記載の皮膚洗浄剤組成物。
The total content of <26> components (D1), (D2), and (D3) is preferably 0.5% by mass or more, more preferably 0.7% by mass or more in the total composition. 0 mass% or more is still more preferable, 1.6 mass% or less is preferable, 1.4 mass% or less is more preferable, 1.2 mass% or less is still more preferable Any one of said <1>-<25>. Skin cleansing composition.
<27> The water content is preferably 45% by mass or more, more preferably 55% by mass or more, preferably 85% by mass or less, and more preferably 75% by mass or less in the total composition <1>. The skin cleansing composition according to any one of to <26>.
<28> Further, it preferably contains a polyhydric alcohol, more preferably dipropylene glycol, 1,3-butylene glycol, glycerin, propylene glycol, sorbitol, malbitol, diglycerin, raffinose, hexylene glycol, glycerin, propylene The skin cleanser composition according to any one of <1> to <27>, wherein glycol is more preferable.
<29>泡粘度変化が0mPa・s以上であることが好ましく、0〜100mPa・sがより好ましく、5〜80mPa・sがさらに好ましく、10〜70mPa・sがよりさらに好ましく、20〜65mPa・sがさらに好ましく、30〜60mPa・sが特に好ましい前記<1>〜<28>のいずれか1記載の皮膚洗浄剤組成物。
<30>前記<1>〜<29>のいずれか1記載の皮膚洗浄剤を皮膚部に適用して洗浄した後、すすぐ皮膚洗浄方法。
<31>前記<1>〜<29>のいずれか1記載の組成物の皮膚洗浄剤としての使用。
<32>前記<1>〜<29>のいずれか1記載の皮膚洗浄組成物を皮膚部に適用する、皮膚洗浄方法。
<29> The change in foam viscosity is preferably 0 mPa · s or more, more preferably 0 to 100 mPa · s, further preferably 5 to 80 mPa · s, still more preferably 10 to 70 mPa · s, and more preferably 20 to 65 mPa · s. The skin cleanser composition according to any one of the above items <1> to <28>, more preferably 30 to 60 mPa · s.
<30> A method for rinsing the skin after applying the skin cleansing agent according to any one of <1> to <29> to the skin part and cleaning the skin part.
<31> Use of the composition according to any one of <1> to <29> as a skin cleanser.
<32> A skin cleaning method, wherein the skin cleaning composition according to any one of <1> to <29> is applied to a skin part.
〈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)
〈製造例〉
本発明の枠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。
<Production example>
The alkyl ether carboxylic acid of component (A) used in the frame skin cleanser 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。
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 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 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、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。
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)=1:1.19:1.13:0.94:1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 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.
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: 1.19: 1.13: 0.94: 1.
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 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.
実施例中、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, regarding EC2, the alkyl ether carboxylic acids obtained in Production Example 5, Production Example 6 and Production Example 7 were mixed at a mass ratio of 78.75 / 15 / 6.25, respectively. did.
実施例中、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, 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.
実施例中、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, regarding EC4, EC1 obtained in Production Example 1 and alkyl ether carboxylic acid obtained in Production Example 4 were mixed in a mass ratio of 40/60 to obtain EC4.
実施例中、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, 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.
実施例で使用した成分(A)の構成は、表1及び表2に示すとおりである。
また、実施例で使用した市販のアルキルエーテルカルボン酸(AKYPO RLM45(花王社製))の平均EO付加モル数は、各社販売元のカタログ値、ホームページで公開されている値を参考にした。不明なアルキル組成、n=0の成分量、n=1の成分とn=2の成分の合計量に関しては上記方法で分析した。
The composition of the component (A) used in the examples is as shown in Tables 1 and 2.
Moreover, the average EO addition mole number of the commercially available alkyl ether carboxylic acid (AKYPO RLM45 (made by Kao company)) used in the Example referred to the catalog value of each company vendor, and the value currently published on the homepage. The unknown alkyl composition, the component amount of n = 0, and the total amount of the component of n = 1 and the component of n = 2 were analyzed by the above method.
実施例1〜16、比較例1〜8
表3及び表4に示す組成の皮膚洗浄剤組成物を製造し、洗浄時の泡立ちの早さ、洗浄時の泡のとろみ感、洗浄時の泡の厚み感、すすぎ時のなめらかさ、すすぎ終点でのストップフィーリング、すすぎ終了時の残留感のなさ及びタオルドライ後のしっとり感を評価した。結果を表3及び表4に併せて示す。
Examples 1-16, Comparative Examples 1-8
Manufactures a skin cleanser composition having the composition shown in Table 3 and Table 4, the speed of foaming at the time of washing, the feeling of foaminess at the time of washing, the feeling of thickness of the foam at the time of washing, the smoothness at the time of rinsing, the end point of rinsing Stop feeling at the end of the rinse, no residual feeling at the end of rinsing and moist feeling after towel drying. The results are shown in Table 3 and Table 4 together.
(製造方法)
イオン交換水の配合量の9割相当量及び、必要に応じてグリセリンを70℃まで加温した後、攪拌しながら成分(D3)をゆっくりと加え、均一に分散させた。成分(A)及び(B)を加え、70℃になるまで攪拌した。この後、48%水酸化カリウム水溶液をpH9.5になる量加え、撹拌して均一にした。さらに、成分(D2)を残りのイオン交換水(25℃)に分散させたものを加えた。成分(D1)、成分(C)、必要に応じてエチレングリコールジステアレートを加え、攪拌して均一にした。続いて、撹拌しながら室温まで冷却した後、必要に応じて、香料、エチレンジアミン4酢酸塩を加えて均一になるまで攪拌し、皮膚洗浄剤組成物を得た。
(Production method)
The amount equivalent to 90% of the amount of ion-exchanged water and, if necessary, glycerin was heated to 70 ° C., and then component (D3) was slowly added with stirring to disperse it uniformly. Components (A) and (B) were added and stirred until reaching 70 ° C. Thereafter, a 48% aqueous potassium hydroxide solution was added in an amount to reach pH 9.5, and the mixture was stirred to be uniform. Further, the component (D2) dispersed in the remaining ion-exchanged water (25 ° C.) was added. Component (D1), component (C), and ethylene glycol distearate as necessary were added and stirred to make uniform. Subsequently, after cooling to room temperature while stirring, a fragrance and ethylenediamine tetraacetate were added as necessary and stirred until uniform to obtain a skin cleansing composition.
(評価方法)
左右の前腕部を30℃の水道水で濡らした後、各皮膚洗浄剤組成物1gを手に取り、反対側の前腕部(肘から手首)に直接塗布し、手のひらを腕の軸方向に20往復させ泡立てた。このときの前腕部の泡の様子から、洗浄時の泡立ちの早さを評価した。また、20回往復したときの16回から20回目における前腕部と手のひらの感触から、泡のとろみ感、泡の厚み感を評価した。
続いて、30℃の水道水ですすぎ、その際に、前腕と手のひらを摺り合わせながらすすぎを行い、すすぎ時のなめらかさ、すすぎ終了時の残留感のなさ、すすぎ終わり時に手のひらが止まる感じ(すすぎ終点でのストップフィーリング)を評価した。さらにタオルドライ後、肌のしっとりする感じについて評価した。
各評価は、以下の基準で行い、結果は、パネラー3名の平均値で示した。
(Evaluation method)
After wetting the left and right forearms with 30 ° C. tap water, take 1 g of each skin cleanser composition and apply it directly to the opposite forearm (from the elbow to the wrist) and place the palm in the axial direction of the arm. It was reciprocated and bubbled. The speed of foaming at the time of washing was evaluated from the state of foam in the forearm at this time. In addition, from the feel of the forearm and palm from the 16th to the 20th time when reciprocating 20 times, the feeling of foam thickening and the thickness of the foam were evaluated.
Next, rinse with tap water at 30 ° C. Rinse the forearm with the palm of your hand, smoothness at the time of rinsing, no residual feeling at the end of rinsing, feeling that the palm stops at the end of rinsing (rinse The stop feeling at the end point was evaluated. Furthermore, after towel drying, it evaluated about the moist feeling of skin.
Each evaluation was performed according to the following criteria, and the result was shown as an average value of three panelists.
(1)洗浄時の泡立ちの早さ:
5;泡立ちが早いと感じた。
4;泡立ちがやや早いと感じた。
3;どちらともいえない。
2;泡立ちがやや遅いと感じた。
1;泡立ちが遅いと感じた。
(1) Speed of foaming during cleaning:
5; I felt that foaming was fast.
4; I felt that foaming was a little quick.
3; Neither can be said.
2; I felt that foaming was a little slow.
1; I felt that foaming was slow.
(2)洗浄時の泡のとろみ感:
5;とろみのあるなめらかな泡と感じた。
4;ややとるみのあるなめらかな泡と感じた。
3;どちらともいえない。
2;泡のとろみがややないと感じた。
1;泡のとろみがないと感じた。
(2) Thickness of foam during washing:
5; I felt a thick and smooth foam.
4; I felt it was a smooth bubble with a little bit.
3; Neither can be said.
2; I felt that the thickening of the bubbles was not a little.
1; I felt there was no thickening of bubbles.
(3)洗浄時の泡の厚み感:
5;泡の厚みがあると感じた。
4;泡の厚みがややあると感じた。
3;どちらともいえない。
2;泡の厚みがややないと感じた。
1;泡の厚みがないと感じた。
(3) Bubble thickness at the time of washing:
5; I felt that there was foam thickness.
4; I felt that there was a little foam thickness.
3; Neither can be said.
2; I felt that the thickness of the foam was not a little.
1; I felt there was no foam thickness.
(4)すすぎ時のなめらかさ:
5;なめらかであると感じた。
4;ややなめらかであると感じた。
3;どちらともいえない。
2;ややなめらかでないと感じた。
1;なめらかでないと感じた。
(4) Smoothness when rinsing:
5; I felt it was smooth.
4; I felt it was a little smooth.
3; Neither can be said.
2; I felt that it was not smooth.
1; I felt it was not smooth.
(5)すすぎ終点のストップフィーリング:
5;すすぎ終わり時のストップフィーリングが強いと感じた。
4;すすぎ終わり時のストップフィーリングがやや強いと感じた。
3;すすぎ終わり時のストップフィーリングが普通と感じた。
2;すすぎ終わり時のストップフィーリングがやや弱いと感じた。
1;すすぎ終わり時のストップフィーリングが弱いと感じた。
(5) Stop feeling at the end of rinsing:
5; I felt that the stop feeling at the end of rinsing was strong.
4; I felt that the stop feeling at the end of rinsing was somewhat strong.
3; I felt that the stop feeling at the end of rinsing was normal.
2; I felt that the stop feeling at the end of rinsing was somewhat weak.
1; I felt that the stop feeling at the end of rinsing was weak.
(6)すすぎ終了時の残留感のなさ:
5;すすぎ終わり時に残留感がないと感じた。
4;すすぎ終わり時に残留感がややないと感じた。
3;どちらともいえない。
2;すすぎ終わり時に残留感がややあると感じた。
1;すすぎ終わり時に残留感があると感じた。
(6) No residual feeling at the end of rinsing:
5; At the end of rinsing, there was no residual feeling.
4; At the end of rinsing, I felt that there was no residual feeling.
3; Neither can be said.
2; I felt that there was some residual feeling at the end of rinsing.
1; I felt that there was a residual feeling at the end of rinsing.
(7)タオルドライ後の肌のしっとり感:
5;しっとりする。
4;ややしっとりする。
3;どちらともいえない。
2;ややしっとりしない。
1;しっとりしない。
(7) Moist skin feeling after towel drying:
5; Moist.
4; Slightly moist.
3; Neither can be said.
2; Does not moist a little.
1; not moist.
試験例1
実施例2、6、比較例5、7、8の皮膚洗浄剤組成物について、泡粘度変化を調べた。
すなわち、各皮膚洗浄剤組成物6mLをナイロンタオル(20cm×100cm)にとり、35℃水道水90mLを加え、50回擦り合わせて泡立てた。得られた泡のレオロジー測定(ステップずり流動テスト)を以下の条件で行った。
レオメーター:Physica MCR300
測定温度:30℃
測定条件
セル:直径50mmのパラレルプレート,ギャップ0.5mm(PP50/Ti-SN1786; d=0.5 mm)
ずり速度の設定:0.1, 0.3, 1, 3, 10, 30, 100, 300, 1000, 3000 s-1
0.1s-1から3000s-1にかけて、各ずり速度で5秒保持しながら段階的に速度を増した。
測定点数:1秒ごとに5点、各ずり速度で25点ずつ粘度測定(mPa・s)。
測定時間:合計50秒
Test example 1
With respect to the skin cleanser compositions of Examples 2 and 6 and Comparative Examples 5, 7, and 8, changes in foam viscosity were examined.
That is, 6 mL of each skin cleansing composition was placed on a nylon towel (20 cm × 100 cm), 90 mL of 35 ° C. tap water was added, and the resulting mixture was rubbed 50 times to be foamed. Rheology measurement (step shear flow test) of the obtained foam was performed under the following conditions.
Rheometer: Physica MCR300
Measurement temperature: 30 ° C
Measurement condition cell: Parallel plate with a diameter of 50 mm, gap 0.5 mm (PP50 / Ti-SN1786; d = 0.5 mm)
Shear speed setting: 0.1, 0.3, 1, 3, 10, 30, 100, 300, 1000, 3000 s -1
From 0.1 s -1 to 3000 s -1 , the speed was increased stepwise while holding at each shear rate for 5 seconds.
Number of measurement points: Viscosity measurement (mPa · s) at 5 points per second and 25 points at each shear rate.
Measurement time: 50 seconds in total
ずり速度300s-1における5秒後の泡粘度の値(mPa・s:測定開始より40秒後)と、ずり速度1000s-1における5秒後の泡粘度の値(mPa・s:測定開始45秒後)を読み取り、以下の式で泡粘度の変化値を算出した。結果を表5に示す。 The value of the foam viscosity after 5 seconds at a shear rate of 300 s −1 (mPa · s: 40 seconds after the start of measurement) and the value of the foam viscosity after 5 seconds at a shear rate of 1000 s −1 (mPa · s: start of measurement 45) Seconds later), and the change value of the foam viscosity was calculated by the following formula. The results are shown in Table 5.
上記試験より、泡粘度の変化値が、実施例の皮膚洗浄剤組成物ではプラス、比較例の皮膚洗浄剤組成物ではマイナスであった。実施例は、優れた泡のとろみ感と厚み感を感じられる皮膚洗浄剤組成物であるが、特に泡粘度の変化値が大きい実施例2は、とろみ感ある泡のなかでも、弾力があり厚み感がある泡であると感じられた。 From the above test, the change value of the foam viscosity was positive in the skin cleanser composition of the example and negative in the skin cleanser composition of the comparative example. The example is a skin cleanser composition that can feel excellent foam thickness and thickness. In particular, Example 2, which has a large change in foam viscosity, is elastic and thick even in thick foam. I felt it was a bubble with a feeling.
処方例1
実施例1の製造方法と同様にして、下記成分を有する皮膚洗浄剤組成物(pH:9.5、脂肪酸の平均炭素数:13.00、脂肪酸のC12比率:0.57、脂肪酸合計量:14.00、成分(D)の含有量(D1+D2+D3):1.10、D1/(D2+D3):1.75、D2/D3:0.33、D2+D3:0.40、C12/他高級脂肪酸:1.33)を得た。
得られた皮膚洗浄剤組成物は、泡立ちや泡の厚み感、とろみ感に優れ、すすぎ性も良好で、すすぎ後に残留感がなく、しっとり感が得られるものであった。更に、すべりが良くとろみのあるなめらかな泡で全身を洗浄することができ、うるおいのあるなめらかな肌で、やわらかい肌を実感することができた。
Formulation Example 1
In the same manner as in the production method of Example 1, a skin cleanser composition having the following components (pH: 9.5, fatty acid average carbon number: 13.00, fatty acid C12 ratio: 0.57, fatty acid total amount: 14.00, content of component (D) (D1 + D2 + D3): 1.10, D1 / (D2 + D3): 1.75, D2 / D3: 0.33, D2 + D3: 0.40, C12 / other higher fatty acids: 1 .33) was obtained.
The obtained skin cleanser composition was excellent in foaming, foam thickness and thickness, had good rinsing properties, had no residual feeling after rinsing, and had a moist feeling. Furthermore, the whole body could be washed with smooth, smooth and smooth foam, and soft skin with a moist and smooth skin could be realized.
(成分)
EC1 3(質量%)
ラウリン酸 3
ステアリン酸 8
イソステアリン酸 5
ポリオキシエチレン(2)ラウリルエーテル硫酸ナトリウム ※2 0.15
塩化ジメチルジアリルアンモニウム・アクリルアミド共重合体 ※3
0.7
ヒドロキシプロピルグアーガム ※6 0.1
ヒドロキシプロピルメチルセルロース ※8 0.3
ラウリン酸アミドプロピルベタイン 3
エチレングリコールジステアレート 2
EDTA−2Na 適量
香料 適量
48%水酸化カリウム 適量
イオン交換水 残部
合計 100
(component)
EC13 (mass%)
Lauric acid 3
Stearic acid 8
Isostearic acid 5
Polyoxyethylene (2) sodium lauryl ether sulfate * 2 0.15
Dimethyldiallylammonium chloride / acrylamide copolymer * 3
0.7
Hydroxypropyl guar gum * 6 0.1
Hydroxypropyl methylcellulose * 8 0.3
Lauric acid amidopropyl betaine 3
Ethylene glycol distearate 2
EDTA-2Na proper amount perfume appropriate amount 48% potassium hydroxide appropriate amount
Ion exchange water balance
Total 100
処方例2
実施例1の製造方法と同様にして、下記成分を有する皮膚洗浄剤組成物(pH:9.5、脂肪酸の平均炭素数:13.00、脂肪酸のC12比率:0.57、脂肪酸合計量:14.00、成分(D)の含有量(D1+D2+D3):1.10、D1/(D2+D3):1.75、D2/D3:0.33、D2+D3:0.40、C12/他高級脂肪酸:1.33)を得た。
得られた皮膚洗浄剤組成物は、泡立ちや泡の厚み感、とろみ感に優れ、すすぎ性も良好で、すすぎ後に残留感がなく、しっとり感が得られるものであった。更に、すべりが良くとろみのあるなめらかな泡で全身を洗浄することができ、うるおいのあるなめらかな肌で、やわらかい肌を実感することができた。
Formulation example 2
In the same manner as in the production method of Example 1, a skin cleanser composition having the following components (pH: 9.5, fatty acid average carbon number: 13.00, fatty acid C12 ratio: 0.57, fatty acid total amount: 14.00, content of component (D) (D1 + D2 + D3): 1.10, D1 / (D2 + D3): 1.75, D2 / D3: 0.33, D2 + D3: 0.40, C12 / other higher fatty acids: 1 .33) was obtained.
The obtained skin cleanser composition was excellent in foaming, foam thickness and thickness, had good rinsing properties, had no residual feeling after rinsing, and had a moist feeling. Furthermore, the whole body could be washed with smooth, smooth and smooth foam, and soft skin with a moist and smooth skin could be realized.
(成分)
EC6 3(質量%)
ラウリン酸 3
ステアリン酸 8
イソステアリン酸 5
ポリオキシエチレン(2)ラウリルエーテル硫酸ナトリウム ※2 0.15
塩化ジメチルジアリルアンモニウム・アクリルアミド共重合体 ※3
0.7
ヒドロキシプロピルグアーガム ※6 0.1
ヒドロキシプロピルメチルセルロース ※8 0.3
ラウリン酸アミドプロピルベタイン 3
エチレングリコールジステアレート 2
EDTA−2Na 適量
香料 適量
48%水酸化カリウム 適量
イオン交換水 残部
合計 100
(component)
EC63 (mass%)
Lauric acid 3
Stearic acid 8
Isostearic acid 5
Polyoxyethylene (2) sodium lauryl ether sulfate * 2 0.15
Dimethyldiallylammonium chloride / acrylamide copolymer * 3
0.7
Hydroxypropyl guar gum * 6 0.1
Hydroxypropyl methylcellulose * 8 0.3
Lauric acid amidopropyl betaine 3
Ethylene glycol distearate 2
EDTA-2Na proper amount perfume appropriate amount 48% potassium hydroxide appropriate amount
Ion exchange water balance
Total 100
Claims (6)
(A)一般式(1)
で表されるアルキルエーテルカルボン酸又はその塩であって、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の成分を合計で40質量%未満含むアルキルエーテルカルボン酸又はその塩 1〜8質量%、
(B)一般式(2)
で表される脂肪酸 8〜16質量%、
(C)両性界面活性剤 0.5〜7質量%、
(D1)電荷密度が0.5〜4.5meq/gのカチオン化ポリマー、
(D2)ノニオン性のガム類、
(D3)ヒドロキシエチル基又はヒドロキシプロピル基が付加したノニオン性セルロース
を含有し、全脂肪酸に対する炭素数11のアルキル基を有する脂肪酸の質量割合(炭素数11のアルキル基を有する脂肪酸/全脂肪酸)が、0.5〜1である皮膚洗浄剤組成物。 The following components (A), (B), (C) and (D):
(A) General formula (1)
Wherein R 1 has an average carbon number of 10.8 to 12.8, contains 4.3 to 30% by mass of n = 0, and n = 1 An alkyl ether carboxylic acid or a salt thereof containing 1 to 8% by mass,
(B) General formula (2)
8 to 16% by mass of a fatty acid represented by
(C) Amphoteric surfactant 0.5-7% by mass,
(D1) a cationized polymer having a charge density of 0.5 to 4.5 meq / g,
(D2) nonionic gums,
(D3) Nonionic cellulose to which hydroxyethyl group or hydroxypropyl group is added, and the mass ratio of fatty acids having 11 alkyl groups to all fatty acids (fatty acids having 11 alkyl groups / total fatty acids) is The skin cleansing composition which is 0.5-1.
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Citations (5)
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JP2005112946A (en) * | 2003-10-06 | 2005-04-28 | Kao Corp | Cleanser composition |
JP2008179586A (en) * | 2007-01-26 | 2008-08-07 | Kracie Home Products Kk | Creamy skin detergent composition |
JP2011084484A (en) * | 2009-10-13 | 2011-04-28 | Kao Corp | Cleanser composition |
JP2013139439A (en) * | 2011-12-08 | 2013-07-18 | Kao Corp | Skin cleansing agent composition |
JP2013184914A (en) * | 2012-03-07 | 2013-09-19 | Kao Corp | Skin washing agent composition |
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JP2005112946A (en) * | 2003-10-06 | 2005-04-28 | Kao Corp | Cleanser composition |
JP2008179586A (en) * | 2007-01-26 | 2008-08-07 | Kracie Home Products Kk | Creamy skin detergent composition |
JP2011084484A (en) * | 2009-10-13 | 2011-04-28 | Kao Corp | Cleanser composition |
JP2013139439A (en) * | 2011-12-08 | 2013-07-18 | Kao Corp | Skin cleansing agent composition |
JP2013184914A (en) * | 2012-03-07 | 2013-09-19 | Kao Corp | Skin washing agent composition |
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