JPS62226921A - Skin detergent composition - Google Patents
Skin detergent compositionInfo
- Publication number
- JPS62226921A JPS62226921A JP6995686A JP6995686A JPS62226921A JP S62226921 A JPS62226921 A JP S62226921A JP 6995686 A JP6995686 A JP 6995686A JP 6995686 A JP6995686 A JP 6995686A JP S62226921 A JPS62226921 A JP S62226921A
- Authority
- JP
- Japan
- Prior art keywords
- acyl
- weight
- methyl
- salt
- composition
- 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
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 61
- 239000003599 detergent Substances 0.000 title description 4
- 229910052708 sodium Inorganic materials 0.000 claims abstract description 19
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 11
- 150000001875 compounds Chemical class 0.000 claims abstract description 9
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims abstract description 8
- 125000003342 alkenyl group Chemical group 0.000 claims abstract description 8
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 8
- 150000005846 sugar alcohols Polymers 0.000 claims abstract description 8
- 229910052700 potassium Inorganic materials 0.000 claims abstract description 5
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 claims abstract description 4
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 claims abstract description 4
- 235000011187 glycerol Nutrition 0.000 claims abstract description 4
- 239000000600 sorbitol Substances 0.000 claims abstract description 4
- 229910052783 alkali metal Inorganic materials 0.000 claims abstract description 3
- 150000001340 alkali metals Chemical class 0.000 claims abstract description 3
- 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 claims description 18
- 239000011734 sodium Substances 0.000 claims description 18
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 claims description 15
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 6
- 125000004432 carbon atom Chemical group C* 0.000 claims description 6
- -1 polyglycerin Chemical compound 0.000 claims description 6
- 239000000126 substance Substances 0.000 claims description 6
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims description 4
- 239000011591 potassium Substances 0.000 claims description 4
- 235000010356 sorbitol Nutrition 0.000 claims description 3
- 239000002202 Polyethylene glycol Substances 0.000 claims description 2
- 229910052739 hydrogen Inorganic materials 0.000 claims description 2
- 239000001257 hydrogen Substances 0.000 claims description 2
- VQHSOMBJVWLPSR-WUJBLJFYSA-N maltitol Chemical compound OC[C@H](O)[C@@H](O)[C@@H]([C@H](O)CO)O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O VQHSOMBJVWLPSR-WUJBLJFYSA-N 0.000 claims description 2
- 239000000845 maltitol Substances 0.000 claims description 2
- 235000010449 maltitol Nutrition 0.000 claims description 2
- 229940035436 maltitol Drugs 0.000 claims description 2
- 229920001223 polyethylene glycol Polymers 0.000 claims description 2
- PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 claims 2
- 229940058015 1,3-butylene glycol Drugs 0.000 claims 1
- 235000019437 butane-1,3-diol Nutrition 0.000 claims 1
- 229940093476 ethylene glycol Drugs 0.000 claims 1
- 229930195712 glutamate Natural products 0.000 claims 1
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims 1
- 229960004063 propylene glycol Drugs 0.000 claims 1
- 235000013772 propylene glycol Nutrition 0.000 claims 1
- 229960002920 sorbitol Drugs 0.000 claims 1
- 238000005187 foaming Methods 0.000 abstract description 10
- 238000002156 mixing Methods 0.000 abstract description 4
- 238000005406 washing Methods 0.000 abstract description 4
- 230000000052 comparative effect Effects 0.000 description 13
- 239000006071 cream Substances 0.000 description 9
- 239000007864 aqueous solution Substances 0.000 description 8
- 238000011156 evaluation Methods 0.000 description 7
- 239000004698 Polyethylene Substances 0.000 description 4
- KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 4
- 230000002349 favourable effect Effects 0.000 description 4
- KWIUHFFTVRNATP-UHFFFAOYSA-N glycine betaine Chemical compound C[N+](C)(C)CC([O-])=O KWIUHFFTVRNATP-UHFFFAOYSA-N 0.000 description 4
- 229920000573 polyethylene Polymers 0.000 description 4
- ZNYIJXQYUNSKDX-NTISSMGPSA-M sodium;hydron;(2s)-2-(tetradecanoylamino)pentanedioate Chemical compound [Na+].CCCCCCCCCCCCCC(=O)N[C@H](C([O-])=O)CCC(O)=O ZNYIJXQYUNSKDX-NTISSMGPSA-M 0.000 description 4
- 230000007423 decrease Effects 0.000 description 3
- VBICKXHEKHSIBG-UHFFFAOYSA-N 1-monostearoylglycerol Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(O)CO VBICKXHEKHSIBG-UHFFFAOYSA-N 0.000 description 2
- DABQDIXIAXPQFG-UHFFFAOYSA-N 2-[dodecanoyl(methyl)amino]ethanesulfonic acid Chemical compound CCCCCCCCCCCC(=O)N(C)CCS(O)(=O)=O DABQDIXIAXPQFG-UHFFFAOYSA-N 0.000 description 2
- UNWFFCPRJXMCNV-UHFFFAOYSA-N 3-[dodecanoyl(methyl)amino]propanoic acid Chemical compound CCCCCCCCCCCC(=O)N(C)CCC(O)=O UNWFFCPRJXMCNV-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- POJWUDADGALRAB-UHFFFAOYSA-N allantoin Chemical compound NC(=O)NC1NC(=O)NC1=O POJWUDADGALRAB-UHFFFAOYSA-N 0.000 description 2
- 229960003237 betaine Drugs 0.000 description 2
- HVYWMOMLDIMFJA-DPAQBDIFSA-N cholesterol Chemical compound C1C=C2C[C@@H](O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H]([C@H](C)CCCC(C)C)[C@@]1(C)CC2 HVYWMOMLDIMFJA-DPAQBDIFSA-N 0.000 description 2
- 238000004140 cleaning Methods 0.000 description 2
- 229940071124 cocoyl glutamate Drugs 0.000 description 2
- 229940079593 drug Drugs 0.000 description 2
- 239000003814 drug Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- 229940093430 polyethylene glycol 1500 Drugs 0.000 description 2
- IWIUXJGIDSGWDN-UQKRIMTDSA-M sodium;(2s)-2-(dodecanoylamino)pentanedioate;hydron Chemical compound [Na+].CCCCCCCCCCCC(=O)N[C@H](C([O-])=O)CCC(O)=O IWIUXJGIDSGWDN-UQKRIMTDSA-M 0.000 description 2
- 238000003860 storage Methods 0.000 description 2
- MTJZWYHTZFVEGI-INIZCTEOSA-N (2s)-2-(tetradecanoylamino)pentanedioic acid Chemical compound CCCCCCCCCCCCCC(=O)N[C@H](C(O)=O)CCC(O)=O MTJZWYHTZFVEGI-INIZCTEOSA-N 0.000 description 1
- OCWPEQFHKVUBTB-HVDRVSQOSA-N 16-methylheptadecanoic acid;(2s)-5-oxopyrrolidine-2-carboxylic acid Chemical compound OC(=O)[C@@H]1CCC(=O)N1.CC(C)CCCCCCCCCCCCCCC(O)=O OCWPEQFHKVUBTB-HVDRVSQOSA-N 0.000 description 1
- VNUREHWOFQRPGE-UHFFFAOYSA-N 2-[2-dodecyl-1-(2-hydroxyethyl)-4,5-dihydroimidazol-1-ium-1-yl]acetate Chemical group CCCCCCCCCCCCC1=NCC[N+]1(CCO)CC([O-])=O VNUREHWOFQRPGE-UHFFFAOYSA-N 0.000 description 1
- LTQRFSDXNWHXKQ-UHFFFAOYSA-N 2-[methyl(octadecanoyl)amino]ethanesulfonic acid Chemical compound CCCCCCCCCCCCCCCCCC(=O)N(C)CCS(O)(=O)=O LTQRFSDXNWHXKQ-UHFFFAOYSA-N 0.000 description 1
- GXJQMKFJQFGQKV-KHPPLWFESA-N 2-[methyl-[(z)-octadec-9-enoyl]amino]ethanesulfonic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)N(C)CCS(O)(=O)=O GXJQMKFJQFGQKV-KHPPLWFESA-N 0.000 description 1
- TWJNQYPJQDRXPH-UHFFFAOYSA-N 2-cyanobenzohydrazide Chemical compound NNC(=O)C1=CC=CC=C1C#N TWJNQYPJQDRXPH-UHFFFAOYSA-N 0.000 description 1
- GMHCJCQMNYOULB-UHFFFAOYSA-N 3-[methyl(octadecanoyl)amino]propanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(=O)N(C)CCC(O)=O GMHCJCQMNYOULB-UHFFFAOYSA-N 0.000 description 1
- DCVMAYAWOPBYKB-UHFFFAOYSA-N 3-[methyl(tetradecanoyl)amino]propanoic acid Chemical compound CCCCCCCCCCCCCC(=O)N(C)CCC(O)=O DCVMAYAWOPBYKB-UHFFFAOYSA-N 0.000 description 1
- KFYGELIIGMESGJ-UHFFFAOYSA-N 3-aminopropanoic acid;sodium Chemical compound [Na].NCCC(O)=O KFYGELIIGMESGJ-UHFFFAOYSA-N 0.000 description 1
- HRASFKASEOUOPD-UHFFFAOYSA-N 3-oxopyrrolidine-1-carboxylic acid Chemical compound OC(=O)N1CCC(=O)C1 HRASFKASEOUOPD-UHFFFAOYSA-N 0.000 description 1
- ODHCTXKNWHHXJC-VKHMYHEASA-M 5-oxo-L-prolinate Chemical compound [O-]C(=O)[C@@H]1CCC(=O)N1 ODHCTXKNWHHXJC-VKHMYHEASA-M 0.000 description 1
- XZIIFPSPUDAGJM-UHFFFAOYSA-N 6-chloro-2-n,2-n-diethylpyrimidine-2,4-diamine Chemical compound CCN(CC)C1=NC(N)=CC(Cl)=N1 XZIIFPSPUDAGJM-UHFFFAOYSA-N 0.000 description 1
- POJWUDADGALRAB-PVQJCKRUSA-N Allantoin Natural products NC(=O)N[C@@H]1NC(=O)NC1=O POJWUDADGALRAB-PVQJCKRUSA-N 0.000 description 1
- 241001116389 Aloe Species 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- FPVVYTCTZKCSOJ-UHFFFAOYSA-N Ethylene glycol distearate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCCOC(=O)CCCCCCCCCCCCCCCCC FPVVYTCTZKCSOJ-UHFFFAOYSA-N 0.000 description 1
- 239000004378 Glycyrrhizin Substances 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 239000004166 Lanolin Substances 0.000 description 1
- 235000021360 Myristic acid Nutrition 0.000 description 1
- TUNFSRHWOTWDNC-UHFFFAOYSA-N Myristic acid Natural products CCCCCCCCCCCCCC(O)=O TUNFSRHWOTWDNC-UHFFFAOYSA-N 0.000 description 1
- SUZRRICLUFMAQD-UHFFFAOYSA-N N-Methyltaurine Chemical compound CNCCS(O)(=O)=O SUZRRICLUFMAQD-UHFFFAOYSA-N 0.000 description 1
- VDIPNVCWMXZNFY-UHFFFAOYSA-N N-methyl-beta-alanine Chemical compound CNCCC(O)=O VDIPNVCWMXZNFY-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 150000001295 alanines Chemical class 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 229960000458 allantoin Drugs 0.000 description 1
- ZOJBYZNEUISWFT-UHFFFAOYSA-N allyl isothiocyanate Chemical compound C=CCN=C=S ZOJBYZNEUISWFT-UHFFFAOYSA-N 0.000 description 1
- 235000011399 aloe vera Nutrition 0.000 description 1
- 235000001014 amino acid Nutrition 0.000 description 1
- 150000001413 amino acids Chemical class 0.000 description 1
- 230000003872 anastomosis Effects 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 150000001768 cations Chemical group 0.000 description 1
- 235000013351 cheese Nutrition 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 235000012000 cholesterol Nutrition 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- YKDMBTQVKVEMSA-UHFFFAOYSA-N diethylene glycol distearate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCCOCCOC(=O)CCCCCCCCCCCCCCCCC YKDMBTQVKVEMSA-UHFFFAOYSA-N 0.000 description 1
- 229940111071 diethylene glycol distearate Drugs 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 239000003205 fragrance Substances 0.000 description 1
- 229940075507 glyceryl monostearate Drugs 0.000 description 1
- LPLVUJXQOOQHMX-UHFFFAOYSA-N glycyrrhetinic acid glycoside Natural products C1CC(C2C(C3(CCC4(C)CCC(C)(CC4C3=CC2=O)C(O)=O)C)(C)CC2)(C)C2C(C)(C)C1OC1OC(C(O)=O)C(O)C(O)C1OC1OC(C(O)=O)C(O)C(O)C1O LPLVUJXQOOQHMX-UHFFFAOYSA-N 0.000 description 1
- 229960004949 glycyrrhizic acid Drugs 0.000 description 1
- UYRUBYNTXSDKQT-UHFFFAOYSA-N glycyrrhizic acid Natural products CC1(C)C(CCC2(C)C1CCC3(C)C2C(=O)C=C4C5CC(C)(CCC5(C)CCC34C)C(=O)O)OC6OC(C(O)C(O)C6OC7OC(O)C(O)C(O)C7C(=O)O)C(=O)O UYRUBYNTXSDKQT-UHFFFAOYSA-N 0.000 description 1
- 235000019410 glycyrrhizin Nutrition 0.000 description 1
- LPLVUJXQOOQHMX-QWBHMCJMSA-N glycyrrhizinic acid Chemical compound O([C@@H]1[C@@H](O)[C@H](O)[C@H](O[C@@H]1O[C@@H]1C([C@H]2[C@]([C@@H]3[C@@]([C@@]4(CC[C@@]5(C)CC[C@@](C)(C[C@H]5C4=CC3=O)C(O)=O)C)(C)CC2)(C)CC1)(C)C)C(O)=O)[C@@H]1O[C@H](C(O)=O)[C@@H](O)[C@H](O)[C@H]1O LPLVUJXQOOQHMX-QWBHMCJMSA-N 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 230000007794 irritation Effects 0.000 description 1
- 229940039717 lanolin Drugs 0.000 description 1
- 235000019388 lanolin Nutrition 0.000 description 1
- 239000002075 main ingredient Substances 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 239000001788 mono and diglycerides of fatty acids Substances 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 239000008164 mustard oil Substances 0.000 description 1
- 235000014593 oils and fats Nutrition 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229940068918 polyethylene glycol 400 Drugs 0.000 description 1
- XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 description 1
- 159000000001 potassium salts Chemical class 0.000 description 1
- KCQOKZAQSWTPIL-BDQAORGHSA-M potassium;(4s)-5-hydroxy-4-(octadecanoylamino)-5-oxopentanoate Chemical compound [H+].[K+].CCCCCCCCCCCCCCCCCC(=O)N[C@H](C([O-])=O)CCC([O-])=O KCQOKZAQSWTPIL-BDQAORGHSA-M 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 229940071139 pyrrolidone carboxylate Drugs 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 229940045920 sodium pyrrolidone carboxylate Drugs 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- FCBUGCHAVCFTHW-NTISSMGPSA-N sodium;(2s)-2-(tetradecanoylamino)pentanedioic acid Chemical compound [Na].CCCCCCCCCCCCCC(=O)N[C@H](C(O)=O)CCC(O)=O FCBUGCHAVCFTHW-NTISSMGPSA-N 0.000 description 1
- CAVXVRQDZKMZDB-UHFFFAOYSA-M sodium;2-[dodecanoyl(methyl)amino]ethanesulfonate Chemical compound [Na+].CCCCCCCCCCCC(=O)N(C)CCS([O-])(=O)=O CAVXVRQDZKMZDB-UHFFFAOYSA-M 0.000 description 1
- HYRLWUFWDYFEES-UHFFFAOYSA-M sodium;2-oxopyrrolidine-1-carboxylate Chemical compound [Na+].[O-]C(=O)N1CCCC1=O HYRLWUFWDYFEES-UHFFFAOYSA-M 0.000 description 1
- QKHBMQWPOUUMQZ-BDQAORGHSA-M sodium;hydron;(2s)-2-(octadecanoylamino)pentanedioate Chemical compound [Na+].CCCCCCCCCCCCCCCCCC(=O)N[C@H](C(O)=O)CCC([O-])=O QKHBMQWPOUUMQZ-BDQAORGHSA-M 0.000 description 1
- FGFAZPVAUUEKBP-LZUSKFISSA-M sodium;hydron;(2s)-2-[[(z)-octadec-9-enoyl]amino]pentanedioate Chemical compound [Na+].CCCCCCCC\C=C/CCCCCCCC(=O)N[C@H](C(O)=O)CCC([O-])=O FGFAZPVAUUEKBP-LZUSKFISSA-M 0.000 description 1
- 229940035044 sorbitan monolaurate Drugs 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 235000013343 vitamin Nutrition 0.000 description 1
- 239000011782 vitamin Substances 0.000 description 1
- 229940088594 vitamin Drugs 0.000 description 1
- 229930003231 vitamin Natural products 0.000 description 1
- 229920003169 water-soluble polymer Polymers 0.000 description 1
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明は、低温及び高温下においても使用が容易であり
、保存安定性、洗浄性、起泡性及び使用時の感触に優れ
、かつ皮膚に対する刺激の少ないクリーム状皮膚洗浄剤
に関する。Detailed Description of the Invention [Industrial Application Field] The present invention is easy to use even at low and high temperatures, has excellent storage stability, cleansing properties, foaming properties, and texture during use, and is comfortable to the skin. This invention relates to a creamy skin cleansing agent that is less irritating to the skin.
酸性アミノ酸系界面活性剤であるN−アシルグルタミン
酸塩は、皮膚に対する刺激が少なく、洗浄性および起泡
性も良好であるととから、酸性皮膚洗浄剤、特に使用し
易いクリーム状皮膚洗浄剤の基剤として用いられている
。N-acylglutamate, which is an acidic amino acid-based surfactant, is less irritating to the skin and has good cleansing and foaming properties. It is used as a base.
しかし、N−アシルグルタミン酸塩は、多量の油性物質
と共存すると洗浄性および起泡性が低下し、また、これ
を基剤とするクリーム状洗浄剤は、冬期には硬くなって
容器から取出すのが困難となシ、夏期には逆に軟かくな
って容器から流れ出てしまうという問題があった。However, when N-acylglutamate coexists with large amounts of oily substances, its detergency and foaming properties decrease, and cream-like detergents based on N-acylglutamate become hard in winter, making it difficult to remove them from the container. However, there was a problem in that it became soft during the summer and would flow out of the container.
本発明の目的は、低温および高温のいずれにおいても適
度な硬さを有し、従って使い易く。The object of the present invention is to have appropriate hardness at both low and high temperatures, and therefore be easy to use.
油性物質共存下での洗浄性および起泡性が良好であシ、
使用時の感触も良く、かつ皮膚に対する刺激の少ない皮
膚洗浄剤組成物を提供することにある。Good cleaning and foaming properties in the presence of oily substances,
To provide a skin cleansing composition that feels good when used and causes less irritation to the skin.
本発明者らは、N−アシルグルタミン酸塩を含有するク
リーム状皮膚洗浄剤の上述の欠点を改良すべく鋭意研究
した結果、主要成分を所定の組成とすることにより、上
述の欠点を改良できることを見出した。As a result of intensive research aimed at improving the above-mentioned drawbacks of cream skin cleansers containing N-acylglutamate, the present inventors have found that the above-mentioned drawbacks can be improved by adjusting the main ingredients to a predetermined composition. I found it.
即ち1本発明のクリーム状皮膚洗浄剤は、N−アシルグ
ルタミン酸塩、N−アシル−N−メチルタウリン塩、N
−アシル−N−メチル−β−アラニン塩、多価アルコー
ルおよび水を含有することを特徴とする。Namely, 1 the creamy skin cleansing agent of the present invention contains N-acylglutamate, N-acyl-N-methyltaurate, N-acylglutamate, N-acyl-N-methyltaurate,
-Acyl-N-methyl-β-alanine salt, polyhydric alcohol and water.
本発明において用いられるN−アシルグルタミン酸塩と
しては、下記一般式(1)で示されるものが好ましい。As the N-acylglutamate used in the present invention, those represented by the following general formula (1) are preferred.
R,CONHCH−COOMl ・・
・(1)CH2CH2C00M2
(式中、R1は炭素数が7〜21のアルキル基又はアル
ケニル基1M1およびM2はいずれも水素。R, CONHCH-COOMl ・・
-(1) CH2CH2C00M2 (In the formula, R1 is an alkyl group or alkenyl group having 7 to 21 carbon atoms. Both M1 and M2 are hydrogen.
アルカリ金属又はアルカノールアミンから銹導されるカ
チオンである。)
一般式(1)で示される化合物の具体例として、N−ラ
ウロイルグルタミン酸モノナトリウム。It is a cation derived from an alkali metal or an alkanolamine. ) A specific example of the compound represented by the general formula (1) is monosodium N-lauroylglutamate.
N−ミリストイルグルタミン酸モノナトリウム。Monosodium N-myristoylglutamate.
N −i4ルミトイルグルタミン酸モノナトリウム。N-i4 monosodium lumitoylglutamate.
N−ステアロイルグルタミン酸モノナトリウム、N−ス
テアロイルグルタミン酸モノカリウム、N−オレオイル
グルタミン酸モノナトリウム、N−ココイルグルタミン
酸モノナトリウム、N−ココイルグルタミン酸モノトリ
エタノールアミン等を挙げることができる。これらは単
独で用いてもよいが、2種以上を混合して用いてもよい
。Examples include monosodium N-stearoylglutamate, monopotassium N-stearoylglutamate, monosodium N-oleoylglutamate, monosodium N-cocoylglutamate, and monotriethanolamine N-cocoylglutamate. These may be used alone or in combination of two or more.
本発明において用いられるN−アシル−N−メチルタウ
リン塩としては、下記一般式(2)で示されるものが好
ましい。The N-acyl-N-methyltaurine salt used in the present invention is preferably one represented by the following general formula (2).
R2C0NCH2CH2SO3M3 ・・・
(2)CH。R2C0NCH2CH2SO3M3...
(2) CH.
(式中5R2は炭素数が7〜17のアルキル基又はアル
ケニル基1M3はナトリウム又はカリウムである。)
一般式(2)で示される化合物の具体例として、N−ラ
ウロイル−N−メチルタウリン、N−ミリストイル−N
−メチルタウリン、N−バルミトイル−N−メチルタウ
リン、N−ステアロイル−N−メチルタウリン、N−オ
レオイル−N−メチルタウリン、N−ココイル−N−メ
チルタウリンのナトリウム塩、カリウム塩等を挙げるこ
とができる。これらは単独で用いてもよいが、2種以上
を混合して用いてもよい。(In the formula, 5R2 is an alkyl group having 7 to 17 carbon atoms or an alkenyl group 1M3 is sodium or potassium.) Specific examples of the compound represented by the general formula (2) include N-lauroyl-N-methyltaurine, N-lauroyl-N-methyltaurine, -Myristoil-N
- List sodium salts, potassium salts, etc. of methyltaurine, N-valmitoyl-N-methyltaurine, N-stearoyl-N-methyltaurine, N-oleoyl-N-methyltaurine, N-cocoyl-N-methyltaurine, etc. I can do it. These may be used alone or in combination of two or more.
本発明において用いられるN−アシル−N−メチル−β
−アラニン塩としては、下記一般式(3)で示されるも
のが好ましい。N-acyl-N-methyl-β used in the present invention
- As the alanine salt, those represented by the following general formula (3) are preferable.
R3C0NCH2CH2C00M4 ・・・(
3)H3
(式中、R3は炭素数が7〜17のアルキル基又はアル
ケニル基1M4はナトリウム又はカリウムである。)
一般式(3)で示される化合物の具体例として。R3C0NCH2CH2C00M4...(
3) H3 (In the formula, R3 is an alkyl group having 7 to 17 carbon atoms or an alkenyl group 1M4 is sodium or potassium.) As a specific example of the compound represented by general formula (3).
N−ラウロイル−N−メチル−β−アラニン。N-lauroyl-N-methyl-β-alanine.
N−ミリストイル−N−メチル−β−アラニン、N−バ
ルミトイル−N−メチル−β−アラニン。N-myristoyl-N-methyl-β-alanine, N-valmitoyl-N-methyl-β-alanine.
N−ステアロイル−N−メチル−β−アラニン、N−オ
Vy?’(ルーN−メチル−β−アラニン。N-stearoyl-N-methyl-β-alanine, N-oVy? '(Rue N-methyl-β-alanine.
N−ココイル−N−メチル−β−アラニンノナトリウム
塩、カリウム塩等を挙げることができる。これは単独で
用いてもよいが、2種以上を混合して用いてもよい。Examples include N-cocoyl-N-methyl-β-alanine nonodium salt and potassium salt. These may be used alone, or two or more types may be used in combination.
本発明において用いられる多価アルコールとしては、グ
リセリン、ポリグリセリン、エチレングリコール、1.
3−ブチレングリコール、プロピレングリコール、ソル
ビトール、マルチトール、ポリエチレングリコールを挙
げることができ、これらは単独で用いてもよいが、2種
以上を混合して用いてもよい。Examples of polyhydric alcohols used in the present invention include glycerin, polyglycerin, ethylene glycol, 1.
Examples include 3-butylene glycol, propylene glycol, sorbitol, maltitol, and polyethylene glycol, which may be used alone or in combination of two or more.
N−アシルグルタミン酸塩の配合量は1組成吻合体に対
して10〜40重量%の範囲が好ましく、15〜30重
量の範囲が特に好ましい。The amount of N-acylglutamate to be blended is preferably in the range of 10 to 40% by weight, particularly preferably in the range of 15 to 30% by weight, based on the one-component anastomoses.
10重量%未満でけ起泡力が低下し、かつ粘度が低くな
シ、一方40重量%を越えると組成物が低温で硬くなる
ため好ましくない。If it is less than 10% by weight, the foaming power will decrease and the viscosity will be low, while if it exceeds 40% by weight, the composition will become hard at low temperatures, which is not preferable.
N−アシル−N−メチルタウリン塩の配合量は、組成物
全体に対して0.2〜20重量%の範囲が好ましく、1
〜10重量%の範囲が%に好ましい。0.5重量−未満
では組成物が高温で軟らかくなシ、20重量%を越える
と低温で硬くなるため好ましくない。The amount of N-acyl-N-methyltaurine salt blended is preferably in the range of 0.2 to 20% by weight based on the entire composition, and 1
A range of 10% by weight is preferred. If it is less than 0.5% by weight, the composition will not be soft at high temperatures, and if it exceeds 20% by weight, it will become hard at low temperatures, which is not preferred.
N−アシル−N−メチル−β−アラニン塩)配合量は、
組成物全体に対して0.5〜20重量%の範囲が好まし
く、1〜10重量%の範囲が特に好ましい。0.5重量
%未満では組成物が低温で硬くなシ、また起泡力も低下
し、20重量%を越えると組成物が軟らかくなり、高温
で分離し易くなるため好ましくない。N-acyl-N-methyl-β-alanine salt) blending amount is:
The range is preferably from 0.5 to 20% by weight, and particularly preferably from 1 to 10% by weight, based on the total composition. If it is less than 0.5% by weight, the composition will not be hard at low temperatures and the foaming power will also be reduced, and if it exceeds 20% by weight, the composition will become soft and easily separate at high temperatures, which is not preferred.
多価アルコールの配合量は、組成物全体に対して20〜
50重量%の範囲が好ましく、25〜40重量%の範囲
が特に好ましい。20重量%未満ではN−アシルグルタ
ミン酸塩の溶解が困難となシ、また組成物が硬くなシす
ぎたシして製剤化が困難となる。一方、50重量%を越
えると起泡力が低下し、組成物製造の時点で分離を生ず
るため好ましくない。The blending amount of polyhydric alcohol is 20 to 20% of the total composition.
A range of 50% by weight is preferred, and a range of 25 to 40% by weight is particularly preferred. If it is less than 20% by weight, it will be difficult to dissolve the N-acylglutamate and the composition will be too hard, making it difficult to formulate a formulation. On the other hand, if it exceeds 50% by weight, the foaming power decreases and separation occurs during composition production, which is not preferable.
水の配合量は、組成物全体に対して10〜50重量−の
範囲が好ましく、20〜40重量%の範囲が特に好まし
い。The amount of water blended is preferably in the range of 10 to 50% by weight, particularly preferably in the range of 20 to 40% by weight, based on the entire composition.
本発明の皮膚洗浄剤組成物に対しては、必要に応じて他
の成分を配合することができる。そのような成分として
、脂肪酸、高級アルコール、炭化水素、油脂、ラノリン
、コレステロール、エステル等の過脂剤;グリチルリチ
ン;アラントイン;ビタミン類:トリクロロカルパニリ
ド;2.4.4’−) +J クロロ−2′−ヒドロキ
シジフェニルエーテル;アロエ末、生薬等の薬剤;ポリ
エチレン粒子、植物種子又は殻等を粉砕した粒子である
スクラブ;ピロリドンカルボン酸塩;色素;香料;−調
整剤、水溶性高分子等が挙げられる。Other components may be added to the skin cleansing composition of the present invention as required. Such components include fatty acids, higher alcohols, hydrocarbons, oils and fats, lanolin, cholesterol, superfat agents such as esters; glycyrrhizin; allantoin; vitamins: trichlorocarpanilide; 2.4.4'-) +J chloro- 2'-Hydroxydiphenyl ether; Medicines such as aloe powder and crude drugs; Polyethylene particles, scrubs made from crushed plant seeds or shells, etc.; Pyrrolidone carboxylate; Pigments; Fragrances; Conditioners, water-soluble polymers, etc. It will be done.
本発明の皮膚洗浄剤組成物によると、低温および高温の
いずれにおいても適度な硬さを有し。According to the skin cleansing composition of the present invention, it has appropriate hardness at both low and high temperatures.
従って使い易く、油性物質共存下での洗浄性および起泡
性が良好であシ2使用時の感触も良く、かつ皮膚に対す
る刺激が少ないという優れた結果が発揮される。Therefore, it is easy to use, has good cleaning properties and foaming properties in the coexistence of oily substances, has a good feel when used, and exhibits excellent results in that it is less irritating to the skin.
以下、本発明の実施例と比較例を示し1本発明の効果を
具体的に説明する。なお、各側の説明に先立って各側で
採用した試験方法について説明する。EXAMPLES Hereinafter, Examples and Comparative Examples of the present invention will be shown to specifically explain the effects of the present invention. Before explaining each side, we will explain the test methods adopted by each side.
外観
組成物を製造後、20〜25℃の温度で1日放置した後
、色、均一性、状態等の外観を肉眼で観察した。Appearance After producing the composition, it was allowed to stand for one day at a temperature of 20 to 25°C, and then its appearance, such as color, uniformity, and condition, was observed with the naked eye.
保存安定性
組成物をポリエチレンチー−プに詰めたものを35℃に
維持された恒温槽中に6ケ月間放置した後の状態を観察
し1分離を生じたシ均−性を失なったものを「不安定」
、均一状態を保ったものを「安定」と評価した。A storage-stable composition packed in a polyethylene chip was left in a constant temperature bath maintained at 35°C for 6 months, and its condition was observed. "unstable"
, those that maintained a uniform state were evaluated as "stable".
チューブからの出し易さ
組成物をポリエチレンチューブに詰めたものを5℃に維
持された恒温槽中に5日間放置し、女性パネラ−20名
によって下記の基準に従って評価し、評価点の合計を人
数平均した値を評価値とした。Ease of removal from tube The composition packed in a polyethylene tube was left in a constant temperature bath maintained at 5°C for 5 days, and evaluated by 20 female panelists according to the following criteria, and the total evaluation score was calculated based on the number of people. The average value was taken as the evaluation value.
4点:軽く力を加えるだけで容易に押出せる3点:多少
力を加えれば比較的容易に押出せる2点:比較的強く押
せば押し出せる
1点:かなり強い力を加えても出し難い保型性
組成物をポリエチレンチー−デに詰めたものを35℃に
維持された恒温槽中に5日間放置し。4 points: Can be easily pushed out by applying a light force. 3 points: Can be pushed out relatively easily by applying some force. 2 points: Can be pushed out by relatively strong pressure. 1 point: Can be pushed out with a relatively strong force. A polyethylene cheese filled with the molding composition was left in a constant temperature bath maintained at 35° C. for 5 days.
女性ノ4ネラー20名によって下記の基準に従って評価
し、評価点の合計を人数平均した値を評価値とした。Evaluations were made by 20 female 4ners according to the following criteria, and the evaluation value was the average of the total evaluation scores.
4点:押出した組成物の断面にチューブの口元形状がそ
のまま残っている
3点:押出した組成物の断面が多少楕円形になっている
2点:押出した組成物の断面がかなシ横に広がった楕円
形になっている
1点:押出したとき組成物が流れて広がってしまう
泡立ち、洗顔時の感触
女性ノ9ネラー20名による洗顔テストを行ない、下記
の基準に従って評価し、評価点の合計を人数平均した値
を評価値とした。4 points: The shape of the mouth of the tube remains in the cross section of the extruded composition. 3 points: The cross section of the extruded composition is somewhat oval. 2 points: The cross section of the extruded composition is slightly horizontal. 1 item with a wide oval shape: Foaming that causes the composition to flow and spread when extruded, and the feel when washing the face A face washing test was conducted by 20 female 9-year-olds and evaluated according to the following criteria. The evaluation value was the average of the total number of participants.
5点二良い
4点:やや良い
3点:どちらともいえない
2点:あまシ良くない
1点:良くない
実施例1
下記(1)〜(4)の成分をビーカーに入れ、混合溶解
した後、加熱し、70℃の混合物(4)を作った。5 points, 2 good points, 4 points: Somewhat good, 3 points: Neither good nor bad, 2 points: Not good, 1 point: Bad Example 1 After putting the following ingredients (1) to (4) into a beaker and mixing and dissolving them. , to make a mixture (4) at 70°C.
(1) ポリエチレングリコール1500 10
重量%(2) プロピレングリコール 25
〃(3) ピロリドンカルボン酸す) IJ ’
7ム 4 〃50%水溶液
(4) 水
17 tt計56〃
次に、下記(5)〜(7)の成分を上記混合物(N中に
添加して攪拌溶解し、70℃の混合物ω)を作った。(1) Polyethylene glycol 1500 10
Weight% (2) Propylene glycol 25
(3) Pyrrolidone carboxylic acid) IJ'
7mu 4 〃50% aqueous solution (4) Water
17 tt total 56 Next, the following components (5) to (7) were added to the above mixture (N and stirred and dissolved to prepare a mixture ω at 70°C).
(5)N−ミリストイルグルタミン酸 20重量%
モノナトリウム
(6) N−ココイル−N−メチルタウリン 8
〃ナトリウム 30%水溶液
(7)N−ココイル−N−メチル−β−アラ 10
〃ニンナトリウム 25%水溶液
8 N
別途、下記(8)〜αつの成分をビーカーに入れ。(5) N-myristoylglutamic acid 20% by weight
Monosodium (6) N-cocoyl-N-methyltaurine 8
〃Sodium 30% aqueous solution (7) N-cocoyl-N-methyl-β-ara 10
〃Nin sodium 25% aqueous solution 8 N Separately, put the following ingredients (8) to α into a beaker.
加温溶解して70℃の混合物(C)を作った。A mixture (C) was prepared by heating and dissolving at 70°C.
(8) ミリスチン酸 2重量%(9
) モノピログルタミン酸モノイソステアリ 2
〃ン酸P、O,E(40モル)硬化とマシ油(至) ソ
ルビタンモノラウレート 1 〃α■ エチ
レングリコールジステアレート 1 〃6
〃
上記混合物(B)に混合物(C)を添加し、70℃で1
0分間攪拌して均一にした後、減圧下で室温まで攪拌冷
却して、均質安定なりリーム状組成物を得た。(8) Myristic acid 2% by weight (9
) Monopyroglutamic acid monoisostearyl 2
〃P, O, E (40 mol) hardening and mustard oil (to) Sorbitan monolaurate 1 〃α■ Ethylene glycol distearate 1 〃6
〃 Add mixture (C) to the above mixture (B) and heat at 70°C for 1
After stirring for 0 minutes to make the mixture uniform, the mixture was stirred and cooled to room temperature under reduced pressure to obtain a homogeneous and stable cream composition.
実施例2
実施例1において、混合物(ト)の成分として下記成分
(1)〜(4)を用い、混合物囚に添加される成分とし
て下記成分(5)〜(7)を用い、混合物(C)の成分
として下記成分(9)〜α)を用いたことを除き、実施
例1と同様の手順で均質安定なりリーム状組成物を得た
。Example 2 In Example 1, the following components (1) to (4) were used as the components of the mixture (G), the following components (5) to (7) were used as the components added to the mixture, and the mixture (C) was A homogeneous and stable cream-like composition was obtained in the same manner as in Example 1, except that the following components (9) to α) were used as components of (a).
(1) ポリエチレングリコール400
20重量%(2) ソルビトール 1
5 〃(3) ピロリドンカルボン酸ナトリウム
5 〃50%水溶液
(4)水 20〃
(5) N−ラウロイルグルタミン酸モノナトリウ
ム 22 〃(6) N−ラウロイル−N−メ
チルタウリンナトリウム 5 〃(7) N−
ラウロイル−N−メチル−β−アラニン 8 〃ナ
トリウム30%水溶液
(8) モノピログルタミン酸モノイソステアリン
酸 3 〃P、O,E、(25モル)グリセリン
(9) グリセリールモノステアレート
1 〃αOジエチレングリコールジステアレート
1 〃■ 比較例I
N−ミリストイルグルタミン酸モノナトリウ状組成物を
得た。(1) Polyethylene glycol 400
20% by weight (2) Sorbitol 1
5 (3) Sodium pyrrolidone carboxylate
5 50% aqueous solution (4) Water 20 (5) Monosodium N-lauroylglutamate 22 (6) Sodium N-lauroyl-N-methyltaurate 5 (7) N-
Lauroyl-N-methyl-β-alanine 8 30% sodium aqueous solution (8) Monopyroglutamic acid monoisostearic acid 3 P, O, E, (25 mol) glycerin (9) Glyceryl monostearate
1 αO diethylene glycol distearate
1 Comparative Example I An N-myristoylglutamic acid monosodium composition was obtained.
■ 比較例2
N−ココイル−N−メチルタウリンナトリウム30%水
溶液の代シに2−ラウリル−N−力ル?キシメチルーN
−ヒドロキシエチルイミダゾリニウムベタイン30q6
を用いたことを除いて実施例1と同様の手順でクリーム
状組成物を得た。■ Comparative Example 2 2-lauryl-N-trichloride instead of 30% aqueous solution of sodium N-cocoyl-N-methyltaurate? xymethyl-N
-Hydroxyethylimidazolinium betaine 30q6
A cream composition was obtained in the same manner as in Example 1, except that .
■ 比較例3
N −=t :Iイル−N−メーF−ルーβ−アラニン
ナトリウム25%水溶液の代りに2−ラウリル−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25%水溶液を用いたことを除いて実施例1
と同様の手順でクリーム状組成物を得た。■ Comparative Example 3 N -=t: Iyl-N-meF-ru β-alanine sodium 25% aqueous solution was replaced with 2-lauryl-N-carboxymethyl-N-hydroxyethylimidazolinium betaine 25% aqueous solution. Example 1 except that
A cream composition was obtained in the same manner as above.
■ 比較例4
ポリエチレングリコール150010%とプロピレング
リコール25%の代りにエタノール35%を用いたこと
を除いて、実施例1と同様の手順でクリーム状組成物を
得た。Comparative Example 4 A cream composition was obtained in the same manner as in Example 1, except that 35% ethanol was used instead of 10% polyethylene glycol 1500 and 25% propylene glycol.
以上の実施例1.2および比較例1〜4のクリーム状組
成物について各性能を評価した結果を下記第1表に示す
。The results of evaluating each performance of the creamy compositions of Example 1.2 and Comparative Examples 1 to 4 are shown in Table 1 below.
第1表
第1表から明らかなように、実施例1および2のクリー
ム状組成物は、外観、保存安定性。Table 1 As is clear from Table 1, the cream compositions of Examples 1 and 2 had good appearance and storage stability.
チューブからの出し易さ、保型性が良好であり。It is easy to take out from the tube and has good shape retention.
泡立ちや洗顔時の感触も優れている。これに対し5本発
明の範囲外の成分を用いた比較例1〜4の組成物は、い
ずれも良好な性能を示していない。It lathers well and feels great when washing your face. On the other hand, none of the compositions of Comparative Examples 1 to 4 using components outside the scope of the present invention exhibited good performance.
比較例5〜7
■ 比較例5
N−ココイル−N−メチルタウリンナトリウムおよびN
−ココイル−N−メチル−β−アラニンナトリウムの代
わシにN−ミリストイルグルタミン酸モノナトリウムを
用いたことを除いて、実施例1と同様の手順でクリーム
状組成物を得た。Comparative Examples 5 to 7 ■ Comparative Example 5 Sodium N-cocoyl-N-methyltaurate and N
A cream composition was obtained in the same manner as in Example 1, except that monosodium N-myristoylglutamate was used instead of sodium cocoyl-N-methyl-β-alanine.
■ 比較例6
N−ココイル−N−メチルタウリンナトリウムの代りに
N−ココイル−N−メチル−β−アラニンナトリウムを
用いたことを除いて、実施例1と同様の手順でクリーム
状組成物を得た。■ Comparative Example 6 A cream composition was obtained in the same manner as in Example 1, except that sodium N-cocoyl-N-methyl-β-alanine was used instead of sodium N-cocoyl-N-methyltaurate. Ta.
■ 比較例7
N −:lI :r イル−N−メチル−β−アラニン
ナトリウムの代わシにN−ココイル−N−メチルタウリ
ンナトリウムを用いたことを除いて、実施例1と同様の
手順でクリーム状組成物を得た。■ Comparative Example 7 N-:lI:r A cream was prepared in the same manner as in Example 1, except that sodium N-cocoyl-N-methyltaurate was used instead of sodium yl-N-methyl-β-alanine. A composition was obtained.
比較例5〜7の組成物の評価結果を下記第2表に示す。The evaluation results of the compositions of Comparative Examples 5 to 7 are shown in Table 2 below.
第2表
第2表から明らかなように、本発明の必須成分であるN
−アシル−N−メチルタウリン塩およびN−アシル−N
−メチル−β−アラニン塩の両方又はいずれかを含まな
い比較例5〜7の組成物は性能が劣っている。Table 2 As is clear from Table 2, N is an essential component of the present invention.
-Acyl-N-methyltaurine salt and N-acyl-N
The compositions of Comparative Examples 5 to 7 that do not contain either or both of the -methyl-β-alanine salts have poor performance.
実施例3
N−ミリストイルグルタミン酸モノナトリウムの含有量
を変化させ、全体が100重量%となるように水の配合
量を調整したことを除いて、実施例1と同様の手順で7
種の組成物を調製し。Example 3 7 was prepared in the same manner as in Example 1, except that the content of monosodium N-myristoylglutamate was changed and the amount of water was adjusted so that the total amount was 100% by weight.
Prepare seed composition.
それらの性能を評価したところ、下記第3表に示す結果
を得た。When their performance was evaluated, the results shown in Table 3 below were obtained.
第3表
第3表から明らかなように、N−ミリストイルグルタミ
ン酸モノナトリウムの含有量が15〜30重量−のとき
に特に好ましい結果が得られることがわかる。As is clear from Table 3, particularly favorable results are obtained when the content of monosodium N-myristoylglutamate is 15 to 30% by weight.
実施例4
N−ココイル−N−メチルタウリンナトリウムの含有量
を変化させ、全体が100重量%となるように水の配合
量を調整したことを除いて。Example 4 Except for changing the content of sodium N-cocoyl-N-methyltaurate and adjusting the amount of water blended so that the total amount was 100% by weight.
−21= 実施例1と同様の手順で8種の組成物を調製し。−21= Eight types of compositions were prepared in the same manner as in Example 1.
それらの性能を評価したところ、下記第4表に示す結果
を得た。When their performance was evaluated, the results shown in Table 4 below were obtained.
第4表
第4表から明らかなように、N−ココイル−N−メチル
タウリンナトリウムの含有量が1〜10重量−のときに
特に好ましい結果が得られることがわかる。Table 4 As is clear from Table 4, particularly favorable results are obtained when the content of sodium N-cocoyl-N-methyltaurate is 1 to 10% by weight.
実施例5
N−ココイル−N−メチル−β−アラニンナトリウムの
含有量を変化させ、全体が100重量%となるように水
の配合量を調整したことを除いて、実施例1と同様の手
順で8種の組成物を調製し、それらの性能を評価したと
ころ、下記第5表に示す結果を得た。Example 5 The same procedure as in Example 1 except that the content of sodium N-cocoyl-N-methyl-β-alanine was changed and the amount of water was adjusted so that the total amount was 100% by weight. When eight types of compositions were prepared and their performances were evaluated, the results shown in Table 5 below were obtained.
第5表
第5表から明らかなように、N−ココイル−N−メチル
−β−アラニンナトリウムの含有量が1〜10重量%の
ときに特に好ましい結果が得られることがわかる。Table 5 As is clear from Table 5, particularly favorable results are obtained when the content of sodium N-cocoyl-N-methyl-β-alanine is 1 to 10% by weight.
実施例6
プロピレングリコールの含有量を変化させ、全体が10
0重量%となるように水の配合量を調整したことを除い
て、実施例1と同様の手順で8種の組成物を調製し、そ
れらの性能を評価したところ、下記第6表に示す結果を
得た。Example 6 The content of propylene glycol was changed, and the total amount was 10
Eight types of compositions were prepared in the same manner as in Example 1, except that the amount of water was adjusted to 0% by weight, and their performance was evaluated. The results are shown in Table 6 below. Got the results.
第6表
第6表から明らかなように、多価アルコールの含有量が
25〜40重量%のときに特に好ましい結果が得られる
ことがわかる。Table 6 As is clear from Table 6, particularly favorable results are obtained when the polyhydric alcohol content is 25 to 40% by weight.
Claims (6)
チルタウリン塩、N−アシル−N−メチル−β−アラニ
ン塩、多価アルコールおよび水を含有することを特徴と
する皮膚洗浄剤組成物。(1) A skin cleansing composition containing N-acylglutamate, N-acyl-N-methyltaurine salt, N-acyl-N-methyl-β-alanine salt, polyhydric alcohol, and water. .
)で示される化合物の1種又は2種以上からなる特許請
求の範囲第1項記載の皮膚洗浄剤組成物。 ▲数式、化学式、表等があります▼・・・(1) (式中、R_1は炭素数が7〜21のアルキル基又はア
ルケニル基、M_1およびM_2はいずれも水素、アル
カリ金属又はアルカノールアミンから誘導されるカチオ
ンである。)(2) The N-acylglutamate has the following general formula (1
2. The skin cleansing composition according to claim 1, which comprises one or more compounds represented by the following formulas. ▲There are mathematical formulas, chemical formulas, tables, etc.▼...(1) (In the formula, R_1 is an alkyl group or alkenyl group having 7 to 21 carbon atoms, and M_1 and M_2 are both derived from hydrogen, an alkali metal, or an alkanolamine. )
一般式(2)で示される化合物の1種又は2種以上から
なる特許請求の範囲第1項記載の皮膚洗浄剤組成物。 ▲数式、化学式、表等があります▼・・・(2) (式中、R_2は炭素数が7〜17のアルキル基又はア
ルケニル基、M_3はナトリウム又はカリウムである。 )(3) The skin cleansing composition according to claim 1, wherein the N-acyl-N-methyltaurine salt comprises one or more compounds represented by the following general formula (2). ▲There are mathematical formulas, chemical formulas, tables, etc.▼...(2) (In the formula, R_2 is an alkyl group or alkenyl group having 7 to 17 carbon atoms, and M_3 is sodium or potassium.)
下記一般式(3)で示される化合物の1種又は2種以上
からなる特許請求の範囲第1項記載の皮膚洗浄剤組成物
。 ▲数式、化学式、表等があります▼・・・(3) (式中、R_3は炭素数が7〜17のアルキル基又はア
ルケニル基、M_4はナトリウム又はカリウムである。 )(4) The N-acyl-N-methyl-β alanine salt is
The skin cleansing composition according to claim 1, which comprises one or more compounds represented by the following general formula (3). ▲There are mathematical formulas, chemical formulas, tables, etc.▼...(3) (In the formula, R_3 is an alkyl group or alkenyl group having 7 to 17 carbon atoms, and M_4 is sodium or potassium.)
リン、エチレングリコール、1,3−ブチレングリコー
ル、プロピレングリコール、ソルビトール、マルチトー
ル、ポリエチレングリコールの1種又は2種以上からな
る特許請求の範囲第1項記載の皮膚洗浄剤組成物。(5) Claim 1, wherein the polyhydric alcohol is one or more of glycerin, polyglycerin, ethylene glycol, 1,3-butylene glycol, propylene glycol, sorbitol, maltitol, and polyethylene glycol. The skin cleansing composition described.
%、前記N−アシル−N−メチルタウリン塩を0.5〜
20重量%、前記N−アシル−N−メチル−β−アラニ
ン塩を0.5〜20重量%、前記多価アルコールを20
〜50重量%、前記水を10〜50重量%含有する特許
請求の範囲第1項記載の皮膚洗浄剤組成物。(6) 10 to 40% by weight of the N-acyl glutamate and 0.5 to 40% by weight of the N-acyl-N-methyltaurine salt.
20% by weight, 0.5 to 20% by weight of the N-acyl-N-methyl-β-alanine salt, and 20% by weight of the polyhydric alcohol.
The skin cleansing composition according to claim 1, containing 10 to 50% by weight of the water.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP6995686A JPH0723297B2 (en) | 1986-03-28 | 1986-03-28 | Skin cleanser composition |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP6995686A JPH0723297B2 (en) | 1986-03-28 | 1986-03-28 | Skin cleanser composition |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS62226921A true JPS62226921A (en) | 1987-10-05 |
JPH0723297B2 JPH0723297B2 (en) | 1995-03-15 |
Family
ID=13417611
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP6995686A Expired - Fee Related JPH0723297B2 (en) | 1986-03-28 | 1986-03-28 | Skin cleanser composition |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0723297B2 (en) |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6314706A (en) * | 1986-07-07 | 1988-01-21 | Kobayashi Kooc:Kk | Oil-in-water type emulsion cosmetic |
JPH02212598A (en) * | 1989-02-13 | 1990-08-23 | Kawaken Fine Chem Co Ltd | Liquid detergent composition |
WO2002057399A1 (en) * | 2001-01-18 | 2002-07-25 | Cognis Deutschland Gmbh & Co. Kg | Detergent mixture |
WO2006030990A1 (en) * | 2004-09-17 | 2006-03-23 | Nof Corporation | Detergent composition |
JP2007039350A (en) * | 2005-08-01 | 2007-02-15 | Lion Corp | Skin cleanser composition |
JP2009067947A (en) * | 2007-09-14 | 2009-04-02 | Ajinomoto Co Inc | Creamy detergent composition |
-
1986
- 1986-03-28 JP JP6995686A patent/JPH0723297B2/en not_active Expired - Fee Related
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6314706A (en) * | 1986-07-07 | 1988-01-21 | Kobayashi Kooc:Kk | Oil-in-water type emulsion cosmetic |
JPH02212598A (en) * | 1989-02-13 | 1990-08-23 | Kawaken Fine Chem Co Ltd | Liquid detergent composition |
WO2002057399A1 (en) * | 2001-01-18 | 2002-07-25 | Cognis Deutschland Gmbh & Co. Kg | Detergent mixture |
WO2006030990A1 (en) * | 2004-09-17 | 2006-03-23 | Nof Corporation | Detergent composition |
JPWO2006030990A1 (en) * | 2004-09-17 | 2008-05-15 | 日油株式会社 | Cleaning composition |
JP2007039350A (en) * | 2005-08-01 | 2007-02-15 | Lion Corp | Skin cleanser composition |
JP2009067947A (en) * | 2007-09-14 | 2009-04-02 | Ajinomoto Co Inc | Creamy detergent composition |
Also Published As
Publication number | Publication date |
---|---|
JPH0723297B2 (en) | 1995-03-15 |
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