JPS63277608A - Composition for skin and hair - Google Patents
Composition for skin and hairInfo
- Publication number
- JPS63277608A JPS63277608A JP11402987A JP11402987A JPS63277608A JP S63277608 A JPS63277608 A JP S63277608A JP 11402987 A JP11402987 A JP 11402987A JP 11402987 A JP11402987 A JP 11402987A JP S63277608 A JPS63277608 A JP S63277608A
- Authority
- JP
- Japan
- Prior art keywords
- water
- soluble
- chitin
- alkyl
- present
- 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 24
- 229920002101 Chitin Polymers 0.000 claims abstract description 46
- 229910052783 alkali metal Inorganic materials 0.000 claims abstract description 5
- 150000001340 alkali metals Chemical group 0.000 claims abstract description 5
- 150000001412 amines Chemical class 0.000 claims abstract description 5
- 150000001413 amino acids Chemical class 0.000 claims abstract description 5
- 239000000126 substance Substances 0.000 claims abstract description 3
- 229920001661 Chitosan Polymers 0.000 abstract description 15
- 239000003945 anionic surfactant Substances 0.000 abstract description 11
- 125000000217 alkyl group Chemical group 0.000 abstract description 7
- 239000006071 cream Substances 0.000 abstract description 7
- 239000006210 lotion Substances 0.000 abstract description 5
- 125000003342 alkenyl group Chemical group 0.000 abstract description 4
- 239000002585 base Substances 0.000 abstract description 4
- 239000003906 humectant Substances 0.000 abstract description 3
- 239000007788 liquid Substances 0.000 abstract description 3
- 238000002156 mixing Methods 0.000 abstract description 3
- 238000011282 treatment Methods 0.000 abstract description 3
- 230000002378 acidificating effect Effects 0.000 abstract description 2
- 239000002453 shampoo Substances 0.000 abstract description 2
- 150000003839 salts Chemical class 0.000 abstract 1
- 238000005406 washing Methods 0.000 abstract 1
- -1 alkyl alkyl taurine salt Chemical class 0.000 description 25
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 19
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 18
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 18
- 230000000052 comparative effect Effects 0.000 description 17
- 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 15
- 230000000694 effects Effects 0.000 description 15
- 239000003755 preservative agent Substances 0.000 description 15
- 239000008213 purified water Substances 0.000 description 15
- 229910052708 sodium Inorganic materials 0.000 description 15
- 239000011734 sodium Substances 0.000 description 15
- PRAKJMSDJKAYCZ-UHFFFAOYSA-N squalane Chemical compound CC(C)CCCC(C)CCCC(C)CCCCC(C)CCCC(C)CCCC(C)C PRAKJMSDJKAYCZ-UHFFFAOYSA-N 0.000 description 12
- 235000011187 glycerol Nutrition 0.000 description 10
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 10
- 239000003240 coconut oil Substances 0.000 description 9
- 235000019864 coconut oil Nutrition 0.000 description 9
- XOAAWQZATWQOTB-UHFFFAOYSA-N taurine Chemical compound NCCS(O)(=O)=O XOAAWQZATWQOTB-UHFFFAOYSA-N 0.000 description 9
- 235000014113 dietary fatty acids Nutrition 0.000 description 8
- 239000000194 fatty acid Substances 0.000 description 8
- 229930195729 fatty acid Natural products 0.000 description 8
- 239000003205 fragrance Substances 0.000 description 8
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 7
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- 230000003796 beauty Effects 0.000 description 6
- 125000004432 carbon atom Chemical group C* 0.000 description 6
- BXWNKGSJHAJOGX-UHFFFAOYSA-N hexadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 description 6
- JXTPJDDICSTXJX-UHFFFAOYSA-N n-Triacontane Natural products CCCCCCCCCCCCCCCCCCCCCCCCCCCCCC JXTPJDDICSTXJX-UHFFFAOYSA-N 0.000 description 6
- 230000002335 preservative effect Effects 0.000 description 6
- 229960004063 propylene glycol Drugs 0.000 description 6
- 229940032094 squalane Drugs 0.000 description 6
- 229940104261 taurate Drugs 0.000 description 6
- 229960003080 taurine Drugs 0.000 description 6
- 241000238557 Decapoda Species 0.000 description 5
- SUZRRICLUFMAQD-UHFFFAOYSA-N N-Methyltaurine Chemical compound CNCCS(O)(=O)=O SUZRRICLUFMAQD-UHFFFAOYSA-N 0.000 description 5
- 125000002057 carboxymethyl group Chemical group [H]OC(=O)C([H])([H])[*] 0.000 description 5
- 150000004665 fatty acids Chemical class 0.000 description 5
- 239000004310 lactic acid Substances 0.000 description 5
- 235000014655 lactic acid Nutrition 0.000 description 5
- 239000000463 material Substances 0.000 description 5
- 230000003020 moisturizing effect Effects 0.000 description 5
- VBICKXHEKHSIBG-UHFFFAOYSA-N 1-monostearoylglycerol Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(O)CO VBICKXHEKHSIBG-UHFFFAOYSA-N 0.000 description 4
- 235000001014 amino acid Nutrition 0.000 description 4
- 239000000686 essence Substances 0.000 description 4
- 239000004094 surface-active agent Substances 0.000 description 4
- 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 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 3
- 229960000541 cetyl alcohol Drugs 0.000 description 3
- 230000001815 facial effect Effects 0.000 description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 3
- 239000003921 oil Substances 0.000 description 3
- 235000019198 oils Nutrition 0.000 description 3
- 229920001296 polysiloxane Polymers 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- 238000003860 storage Methods 0.000 description 3
- PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 description 2
- XDOFQFKRPWOURC-UHFFFAOYSA-N 16-methylheptadecanoic acid Chemical compound CC(C)CCCCCCCCCCCCCCC(O)=O XDOFQFKRPWOURC-UHFFFAOYSA-N 0.000 description 2
- 241000894006 Bacteria Species 0.000 description 2
- 241000195493 Cryptophyta Species 0.000 description 2
- 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 description 2
- ZAKOWWREFLAJOT-CEFNRUSXSA-N D-alpha-tocopherylacetate Chemical compound CC(=O)OC1=C(C)C(C)=C2O[C@@](CCC[C@H](C)CCC[C@H](C)CCCC(C)C)(C)CCC2=C1C ZAKOWWREFLAJOT-CEFNRUSXSA-N 0.000 description 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
- 241000238631 Hexapoda Species 0.000 description 2
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 2
- BNIAKAQSIZOVSN-UHFFFAOYSA-N [Na].CC(O)CO Chemical compound [Na].CC(O)CO BNIAKAQSIZOVSN-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 239000012190 activator Substances 0.000 description 2
- 150000005215 alkyl ethers Chemical class 0.000 description 2
- 150000008051 alkyl sulfates Chemical class 0.000 description 2
- 239000004359 castor oil Substances 0.000 description 2
- 235000019438 castor oil Nutrition 0.000 description 2
- 210000002421 cell wall Anatomy 0.000 description 2
- 239000004020 conductor Substances 0.000 description 2
- ZAKOWWREFLAJOT-UHFFFAOYSA-N d-alpha-Tocopheryl acetate Natural products CC(=O)OC1=C(C)C(C)=C2OC(CCCC(C)CCCC(C)CCCC(C)C)(C)CCC2=C1C ZAKOWWREFLAJOT-UHFFFAOYSA-N 0.000 description 2
- SZXQTJUDPRGNJN-UHFFFAOYSA-N dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 description 2
- NOPFSRXAKWQILS-UHFFFAOYSA-N docosan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCCCCCO NOPFSRXAKWQILS-UHFFFAOYSA-N 0.000 description 2
- UKMSUNONTOPOIO-UHFFFAOYSA-N docosanoic acid Chemical compound CCCCCCCCCCCCCCCCCCCCCC(O)=O UKMSUNONTOPOIO-UHFFFAOYSA-N 0.000 description 2
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 2
- 125000003976 glyceryl group Chemical group [H]C([*])([H])C(O[H])([H])C(O[H])([H])[H] 0.000 description 2
- 229940075507 glyceryl monostearate Drugs 0.000 description 2
- 229940057995 liquid paraffin Drugs 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 239000001788 mono and diglycerides of fatty acids Substances 0.000 description 2
- 125000001419 myristoyl group Chemical group O=C([*])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 2
- 229910052700 potassium Inorganic materials 0.000 description 2
- 239000011591 potassium Substances 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- 229920002545 silicone oil Polymers 0.000 description 2
- UKSFMDODPANKJI-UHFFFAOYSA-M sodium;2-[methyl(octadecanoyl)amino]ethanesulfonate Chemical compound [Na+].CCCCCCCCCCCCCCCCCC(=O)N(C)CCS([O-])(=O)=O UKSFMDODPANKJI-UHFFFAOYSA-M 0.000 description 2
- 239000000600 sorbitol Substances 0.000 description 2
- 229940042585 tocopherol acetate Drugs 0.000 description 2
- 229940099259 vaseline Drugs 0.000 description 2
- KIUKXJAPPMFGSW-DNGZLQJQSA-N (2S,3S,4S,5R,6R)-6-[(2S,3R,4R,5S,6R)-3-Acetamido-2-[(2S,3S,4R,5R,6R)-6-[(2R,3R,4R,5S,6R)-3-acetamido-2,5-dihydroxy-6-(hydroxymethyl)oxan-4-yl]oxy-2-carboxy-4,5-dihydroxyoxan-3-yl]oxy-5-hydroxy-6-(hydroxymethyl)oxan-4-yl]oxy-3,4,5-trihydroxyoxane-2-carboxylic acid Chemical compound CC(=O)N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O)[C@@H]1O[C@H]1[C@H](O)[C@@H](O)[C@H](O[C@H]2[C@@H]([C@@H](O[C@H]3[C@@H]([C@@H](O)[C@H](O)[C@H](O3)C(O)=O)O)[C@H](O)[C@@H](CO)O2)NC(C)=O)[C@@H](C(O)=O)O1 KIUKXJAPPMFGSW-DNGZLQJQSA-N 0.000 description 1
- 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
- ALSTYHKOOCGGFT-KTKRTIGZSA-N (9Z)-octadecen-1-ol Chemical compound CCCCCCCC\C=C/CCCCCCCCO ALSTYHKOOCGGFT-KTKRTIGZSA-N 0.000 description 1
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
- 229940058015 1,3-butylene glycol Drugs 0.000 description 1
- VULQAGPYFSUFCA-UHFFFAOYSA-N 16-methylheptadecanoic acid;propane-1,2,3-triol Chemical compound OCC(O)CO.CC(C)CCCCCCCCCCCCCCC(O)=O VULQAGPYFSUFCA-UHFFFAOYSA-N 0.000 description 1
- HYZPVMPQJVVJBP-UHFFFAOYSA-N 2-[bis(2-hydroxyethyl)amino]ethanol;propane-1,2,3-triol Chemical compound OCC(O)CO.OCCN(CCO)CCO HYZPVMPQJVVJBP-UHFFFAOYSA-N 0.000 description 1
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 1
- HIQIXEFWDLTDED-UHFFFAOYSA-N 4-hydroxy-1-piperidin-4-ylpyrrolidin-2-one Chemical compound O=C1CC(O)CN1C1CCNCC1 HIQIXEFWDLTDED-UHFFFAOYSA-N 0.000 description 1
- SQDAZGGFXASXDW-UHFFFAOYSA-N 5-bromo-2-(trifluoromethoxy)pyridine Chemical compound FC(F)(F)OC1=CC=C(Br)C=N1 SQDAZGGFXASXDW-UHFFFAOYSA-N 0.000 description 1
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
- 235000021357 Behenic acid Nutrition 0.000 description 1
- 229920001287 Chondroitin sulfate Polymers 0.000 description 1
- 241000238424 Crustacea Species 0.000 description 1
- 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 description 1
- 239000005639 Lauric acid Substances 0.000 description 1
- 239000005642 Oleic acid Substances 0.000 description 1
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 1
- 239000004264 Petrolatum Substances 0.000 description 1
- 235000008331 Pinus X rigitaeda Nutrition 0.000 description 1
- 235000011613 Pinus brutia Nutrition 0.000 description 1
- 241000018646 Pinus brutia Species 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 229920001214 Polysorbate 60 Polymers 0.000 description 1
- 235000004443 Ricinus communis Nutrition 0.000 description 1
- DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- DRRMRHKHTQRWMB-UHFFFAOYSA-N [3-(2-ethylhexanoyloxy)-2,2-bis(2-ethylhexanoyloxymethyl)propyl] 2-ethylhexanoate Chemical compound CCCCC(CC)C(=O)OCC(COC(=O)C(CC)CCCC)(COC(=O)C(CC)CCCC)COC(=O)C(CC)CCCC DRRMRHKHTQRWMB-UHFFFAOYSA-N 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000001449 anionic compounds Chemical class 0.000 description 1
- 229940121363 anti-inflammatory agent Drugs 0.000 description 1
- 239000002260 anti-inflammatory agent Substances 0.000 description 1
- 239000003899 bactericide agent Substances 0.000 description 1
- 235000015278 beef Nutrition 0.000 description 1
- 229940116226 behenic acid Drugs 0.000 description 1
- 239000000872 buffer Substances 0.000 description 1
- 235000019437 butane-1,3-diol Nutrition 0.000 description 1
- 239000002738 chelating agent Substances 0.000 description 1
- 229940059329 chondroitin sulfate Drugs 0.000 description 1
- 230000003766 combability Effects 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- 230000006196 deacetylation Effects 0.000 description 1
- 238000003381 deacetylation reaction Methods 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 229940113120 dipropylene glycol Drugs 0.000 description 1
- 229960000735 docosanol Drugs 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 239000010696 ester oil Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 235000008524 evening primrose extract Nutrition 0.000 description 1
- 239000010475 evening primrose oil Substances 0.000 description 1
- 229940089020 evening primrose oil Drugs 0.000 description 1
- 229930195712 glutamate Natural products 0.000 description 1
- ZDXPYRJPNDTMRX-UHFFFAOYSA-N glutamine Natural products OC(=O)C(N)CCC(N)=O ZDXPYRJPNDTMRX-UHFFFAOYSA-N 0.000 description 1
- 229960005150 glycerol Drugs 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- OIKBVOIOVNEVJR-UHFFFAOYSA-N hexadecyl 6-methylheptanoate Chemical compound CCCCCCCCCCCCCCCCOC(=O)CCCCC(C)C OIKBVOIOVNEVJR-UHFFFAOYSA-N 0.000 description 1
- 229920002674 hyaluronan Polymers 0.000 description 1
- 229960003160 hyaluronic acid Drugs 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
- 229940119170 jojoba wax Drugs 0.000 description 1
- 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 description 1
- 239000000845 maltitol Substances 0.000 description 1
- 235000010449 maltitol Nutrition 0.000 description 1
- 229940035436 maltitol Drugs 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- LAQFLZHBVPULPL-UHFFFAOYSA-N methyl(phenyl)silicon Chemical compound C[Si]C1=CC=CC=C1 LAQFLZHBVPULPL-UHFFFAOYSA-N 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- XMLQWXUVTXCDDL-UHFFFAOYSA-N oleyl alcohol Natural products CCCCCCC=CCCCCCCCCCCO XMLQWXUVTXCDDL-UHFFFAOYSA-N 0.000 description 1
- 229940055577 oleyl alcohol Drugs 0.000 description 1
- 239000004006 olive oil Substances 0.000 description 1
- 235000008390 olive oil Nutrition 0.000 description 1
- 125000001312 palmitoyl group Chemical group O=C([*])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])C([H])([H])C([H])([H])[H] 0.000 description 1
- 229940056211 paraffin Drugs 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 239000006072 paste Substances 0.000 description 1
- 229940066842 petrolatum Drugs 0.000 description 1
- 235000019271 petrolatum Nutrition 0.000 description 1
- 235000011007 phosphoric acid Nutrition 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229940068918 polyethylene glycol 400 Drugs 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 1
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- AMCPECLBZPXAPB-UHFFFAOYSA-N propane-1,2,3-triol;sodium Chemical compound [Na].OCC(O)CO AMCPECLBZPXAPB-UHFFFAOYSA-N 0.000 description 1
- 235000013772 propylene glycol Nutrition 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 229960002920 sorbitol Drugs 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 125000003696 stearoyl group Chemical group O=C([*])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])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 239000003760 tallow Substances 0.000 description 1
- TUNFSRHWOTWDNC-HKGQFRNVSA-N tetradecanoic acid Chemical compound CCCCCCCCCCCCC[14C](O)=O TUNFSRHWOTWDNC-HKGQFRNVSA-N 0.000 description 1
- 229940088594 vitamin Drugs 0.000 description 1
- 229930003231 vitamin Natural products 0.000 description 1
- 235000013343 vitamin Nutrition 0.000 description 1
- 239000011782 vitamin Substances 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/73—Polysaccharides
- A61K8/736—Chitin; Chitosan; Derivatives thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/46—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing sulfur
- A61K8/466—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing sulfur containing sulfonic acid derivatives; Salts
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q19/00—Preparations for care of the skin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q5/00—Preparations for care of the hair
- A61Q5/02—Preparations for cleaning the hair
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Birds (AREA)
- Epidemiology (AREA)
- Dermatology (AREA)
- Cosmetics (AREA)
Abstract
Description
【発明の詳細な説明】
[産業上の利用分野]
本発明は、処方中に水溶性キチン誘導体の一種または二
種以上と下記一般式で表されるアルキロイルアルキルタ
ウリン塩型陰イオン界面活性剤の一種または二種以上を
配合することにより、使用感、安定性に優れたことを特
徴とする皮膚および毛髪用組成物に関するものである。Detailed Description of the Invention [Industrial Field of Application] The present invention comprises a formulation containing one or more water-soluble chitin derivatives and an alkyl alkyl taurine salt type anionic surfactant represented by the following general formula. The present invention relates to a skin and hair composition characterized by having excellent usability and stability by incorporating one or more of the following.
Rr−C0−N−CH2CR2−S 03M(式中R1
は平均炭素原子数7ないし19のアルキル基または、ア
ルケニル基、R2は平均炭素原子数1ないし3の低級ア
ルキル基、Mはアルカリ金属、有機アミン類、塩基性ア
ミノ酸類を表す。)
[従来の技術]
カニ、エビなどの甲殻顕の殻や昆虫などの外骨格、ある
いは菌、藻類の細胞壁などに存在するキチンおよびその
誘導体は保湿作用、皮膚および毛髪保護作用に優れ天然
由来の高分子物質として皮膚および毛髪用組成物用原料
として着目されているが、通常の原料との相溶性が悪く
皮膚および毛髪用組成物中で均一溶解させることが困難
であった。そのためキチンおよびその水溶性誘導体は皮
膚および毛髪用組成物に配合した場合、優れた保湿作用
、皮膚および毛髪保護作用が期待きれつつも現実の利用
は、難しいものであった。Rr-C0-N-CH2CR2-S 03M (R1 in the formula
represents an alkyl group or alkenyl group having an average of 7 to 19 carbon atoms, R2 represents a lower alkyl group having an average of 1 to 3 carbon atoms, and M represents an alkali metal, an organic amine, or a basic amino acid. ) [Prior art] Chitin and its derivatives, which exist in the shells of crabs, shrimps, etc., the exoskeletons of insects, and the cell walls of bacteria and algae, have excellent moisturizing effects and skin and hair protection effects. Although it has attracted attention as a polymeric material as a raw material for skin and hair compositions, it has poor compatibility with ordinary raw materials and has been difficult to dissolve uniformly in skin and hair compositions. Therefore, when chitin and its water-soluble derivatives are incorporated into skin and hair compositions, although they are expected to have excellent moisturizing and skin and hair protection effects, their actual use has been difficult.
[発明が解決しようとする問題点]
本発明者らは係る事情に鑑み鋭意研究の結果、処方中に
一般式
%式%
(式中R1は平均炭素原子数7ないし19のアルキル基
または、アルケニル基、R2は平均炭素原子数1ないし
3の低級アルキル基、Mはアルカリ金属、有機アミン類
、塩基性アミノ酸類を表す。)で表されるアルキロイル
アルキルタウリン塩型陰イオン界面活性剤の一種または
二種以上とともに水溶性キチン誘導体の一種または二種
以上を配合すれば、使用感、安定性に優れた皮膚および
毛髪用組成物が得られることを見出し本発明を完成する
に至った。[Problems to be Solved by the Invention] In view of the above circumstances, the present inventors have conducted intensive research and have found that formulas containing the general formula % (wherein R1 is an alkyl group having an average number of carbon atoms of 7 to 19 or alkenyl R2 is a lower alkyl group having an average number of carbon atoms of 1 to 3, and M represents an alkali metal, an organic amine, or a basic amino acid. The present inventors have discovered that a skin and hair composition with excellent usability and stability can be obtained by blending one or more water-soluble chitin derivatives together with two or more other types of chitin derivatives.
[問題点を解決するための手段および作用]すなわち本
発明は、処方中に水溶性キチン誘導体の一種または二種
以上とアルキロイルアルキルタウリン塩型陰イオン界面
活性剤の一種または二種以上を配合したことを特徴とす
る使用感、安定性に優れた皮膚および毛髪用組成物を提
供するものである。[Means and effects for solving the problem] That is, the present invention combines one or more water-soluble chitin derivatives and one or more alkyl alkyl taurine salt type anionic surfactants in the formulation. The present invention provides a composition for skin and hair that is characterized by excellent usability and stability.
以下、本発明の構成について詳述する。なお以下の説明
において皮膚および毛髪用組成物を単に組成物と記述す
る。Hereinafter, the configuration of the present invention will be explained in detail. In the following description, the composition for skin and hair will be simply referred to as a composition.
本発明で用いられる水溶性キチン誘導体は、カニ、エビ
などの甲殻類の殻や昆虫などの外骨格、あるいは菌、藻
類の細胞壁などに存在するキチンを原料として誘導され
るもので、その代表的なものとしてはまずキチンの脱ア
セチル化物であるキトサンが例示きれる。The water-soluble chitin derivatives used in the present invention are derived from chitin present in the shells of crustaceans such as crabs and shrimps, the exoskeletons of insects, and the cell walls of bacteria and algae. An example of this is chitosan, which is a deacetylated product of chitin.
キトサンを得る具体的な例としては、カニ、エビの甲殻
を希塩酸で処理して脱炭酸カルシウム処理し、ついで希
水酸化ナトリウム溶液で処理して脱タンパクする。得ら
れた粗キチンを水洗し、必要に応じて精製処理し、つづ
いて濃水酸化ナトリウム溶液で脱アセチル化処理する。As a specific example of obtaining chitosan, crab and shrimp shells are treated with dilute hydrochloric acid to decalcify and then treated with dilute sodium hydroxide solution to deproteinize. The obtained crude chitin is washed with water, purified if necessary, and then deacetylated with a concentrated sodium hydroxide solution.
得られた粗キトサンを水洗し、必要に応じて精製しキト
サンとする。The obtained crude chitosan is washed with water and, if necessary, purified to obtain chitosan.
キチンそのものは一般に水に不溶であるが、ある種の方
法によって処理きれたキチンは水溶性である。すなわち
特開昭53−47479に例示される脱アセチル化度4
0〜60%の水溶性部分脱アセチル化キチンである。こ
の水溶性部分脱アセチル化キチンも本発明に用いること
ができる。Chitin itself is generally insoluble in water, but chitin that has been treated by certain methods is water-soluble. That is, the degree of deacetylation is 4 as exemplified in JP-A No. 53-47479.
It is 0-60% water soluble partially deacetylated chitin. This water-soluble partially deacetylated chitin can also be used in the present invention.
またキチンに置換基を導入して水溶性としたもの、たと
えばカルボキシメチル基を導入したカルボキシメチルキ
チン、グライコール化キチン、キチンサルフェート、な
ども本発明に応用できる。Furthermore, chitin made water-soluble by introducing substituents, such as carboxymethyl chitin with carboxymethyl groups introduced, glycolated chitin, and chitin sulfate, can also be applied to the present invention.
キチンは通常分子量100万以上の高分子であるが、そ
の誘導体は処理過程において分子量の低下がおこり数十
万程度のものもめずらしくない。Chitin is usually a polymer with a molecular weight of 1,000,000 or more, but the molecular weight of its derivatives decreases during the treatment process, and it is not uncommon for chitin to have a molecular weight of several hundred thousand.
本発明に用いられる水溶性キチン誘導体の分子量は天然
に近い100万以上のものから低分子化した致方のもの
まで利用することができる。The water-soluble chitin derivative used in the present invention can range in molecular weight from a natural one of 1,000,000 or more to a low molecular weight one.
本発明において水溶性キチン誘導体を配合する量として
は0.001〜10重量%(以下単に%と記す。)であ
り、0.001%以下の水準では本発明にかかる効果を
発揮しにくく、10%を越える場合には水溶性キチン誘
導体の溶解度を上回り組成物を調製することが困難にな
る。In the present invention, the amount of the water-soluble chitin derivative blended is 0.001 to 10% by weight (hereinafter simply referred to as %), and at a level of 0.001% or less, it is difficult to exhibit the effects of the present invention; If the amount exceeds the solubility of the water-soluble chitin derivative, it becomes difficult to prepare a composition.
本発明の効果を発揮するために配合される量としては好
ましくは0.01〜1%である。The amount added to achieve the effects of the present invention is preferably 0.01 to 1%.
また本発明にかかる水溶性キチン誘導体を溶解する目的
で水溶性キチン誘導体とともに少量の酸性物質を添加し
ても本発明の効果を阻害するものではない。Further, even if a small amount of an acidic substance is added together with the water-soluble chitin derivative for the purpose of dissolving the water-soluble chitin derivative according to the present invention, the effects of the present invention will not be inhibited.
たとえばキトサンを溶解する目的において、キトサン重
量に対して当量の塩酸を併用しても本発明にかかる効果
は不変である。For example, for the purpose of dissolving chitosan, the effects of the present invention remain unchanged even if hydrochloric acid is used in an amount equivalent to the weight of chitosan.
一方本発明で用いられるアルキロイルアルキルタウリン
塩型陰イオン界面活性剤としては一般式
%式%
(式中R1は平均炭素原子数7ないし19のアルキル基
または、アルケニル基、R2は平均炭素原子数1ないし
3の低級アルキル基、Mはアルカリ金属、有機アミン類
、塩基性アミノ酸類を表す。)で表されるものである。On the other hand, the alkyl alkyl taurine salt type anionic surfactant used in the present invention has the general formula % formula % (wherein R1 is an alkyl group or alkenyl group having an average number of carbon atoms of 7 to 19, and R2 is an average number of carbon atoms. 1 to 3 lower alkyl groups, M represents an alkali metal, organic amines, or basic amino acids).
アルキロイルアルキルタウリン塩型陰イオン界面活性剤
としては、ニラコールCMT−30(ココイルメチルタ
ウリンナトリウム)、ニラコールSMT (ステアロイ
ルメチルタウリンナトリウム)、ニラコールPMT (
パルミトイルメチルタウリンナトリウム)、ニラコール
MMT (ミリストイルメチルタウリンナトリウム)、
ニラコールLMT (ラウロイルメチルタウリンナトリ
ウム)などの商品名で市販されているものや、ダイヤボ
ン−L(ラウロイルメチルタウリンナトリウム) 、5
T−1,5T−3F (ココイルメチルタウリンナトリ
ウム)、ホスタボンCTペースト(ココイルメチルタウ
リンナトリウム)などの商品名で市販されているものが
有名である。Examples of alkyl alkyl taurine salt type anionic surfactants include Nylacol CMT-30 (sodium cocoyl methyl taurate), Nylacol SMT (sodium stearoyl methyl taurate), and Nylacol PMT (sodium cocoyl methyl taurate).
palmitoyl methyl taurate sodium), Nilacol MMT (myristoyl methyl taurate sodium),
Those commercially available under trade names such as Niracol LMT (sodium lauroyl methyl taurate), Diabon-L (sodium lauroyl methyl taurate), 5
Famous commercially available products include T-1,5T-3F (sodium cocoyl methyl taurate) and Hostavon CT paste (sodium cocoyl methyl taurate).
本発明に従って水溶性キチン誘導体とともに組成物に配
合されるアルキロイルアルキルタウリン塩型陰イオン界
面活性剤の量としては0.01〜50%であり、好まし
くは0.1〜30%である。According to the present invention, the amount of the alkyl alkyl taurine salt type anionic surfactant mixed into the composition together with the water-soluble chitin derivative is 0.01 to 50%, preferably 0.1 to 30%.
本発明にしたがって水溶性キチン訪導体およびアルキロ
イルアルキルタウリン塩型陰イオン界面活性剤を配合す
る組成物基剤としては通常の液状、クリーム状、乳液状
、ペースト状等の形態の組成物基剤が利用できる。また
本発明にかかる技術は、保湿クリーム、乳化エツセンス
、シャンプー、ヘアトリートメント、ボディクレンザ−
1洗顔用ペースト、洗顔用ローションなどに応用できる
。The composition base in which the water-soluble chitin conductor and the alkyl alkyl taurine salt type anionic surfactant are blended according to the present invention is a composition base in the form of a usual liquid, cream, emulsion, paste, etc. is available. Furthermore, the technology according to the present invention can be applied to moisturizing creams, emulsified essences, shampoos, hair treatments, body cleansers, etc.
1. Can be applied to facial cleansing paste, facial cleansing lotion, etc.
それらの組成物基剤には精製水の他に必要に応じて保湿
剤も配合できる。In addition to purified water, a humectant can also be added to the base of these compositions, if necessary.
例えばグリセリン、1.3−ブチレングリコール、プロ
ピレングリコール、ジプロピレングリコール、ソルビト
ール、マルチトール、ヒアルロン酸、コンドロイチン硫
酸塩、ポリエチレングリコールなどが例示される。Examples include glycerin, 1,3-butylene glycol, propylene glycol, dipropylene glycol, sorbitol, maltitol, hyaluronic acid, chondroitin sulfate, and polyethylene glycol.
油分としては流動パラフィン、スクワラン、ワセリン、
固形パラフィン等の炭化水素、オリーブ油、ポホパ油、
月見草油、ヤシ油、牛脂などの天然油、イソプロピルミ
リステート、ペンタエリスリトール−テトラ−2−エチ
ルヘキサノエート、セチルイソオクタノエートなどのエ
ステル油、メチルシリコン、メチルフェニルシリコンな
どのシリコン油、セチルアルコール、オレイルアルコー
ル、ベヘニルアルコール等の高級アルコール、ステアリ
ン酸、ベヘニン酸、バルミチン酸、ミリスチン酸、ラウ
リン酸、オレイン酸、イソステアリン酸、等の脂肪酸、
等も併用できる。Oils include liquid paraffin, squalane, petrolatum,
Hydrocarbons such as solid paraffin, olive oil, phoppa oil,
Natural oils such as evening primrose oil, coconut oil, beef tallow, ester oils such as isopropyl myristate, pentaerythritol-tetra-2-ethylhexanoate, cetyl isooctanoate, silicone oils such as methyl silicone, methylphenyl silicone, cetyl Alcohol, higher alcohols such as oleyl alcohol and behenyl alcohol, fatty acids such as stearic acid, behenic acid, valmitic acid, myristic acid, lauric acid, oleic acid, isostearic acid, etc.
etc. can also be used together.
界面活性剤としては、通常組成物に配合できるものが応
用できる。As the surfactant, those that can be generally incorporated into the composition can be used.
非イオン性のものとしては、P、OEアルキルエーテル
、POE分岐アルキルエーテル、POEソルビタンエス
テル、POEグリセリン脂肪酸エステル、POE硬化硬
化ヒマシソルビタンエステル、グリセリン脂肪酸エステ
ル、ポリグリセリン脂肪酸エステル、等が一般的である
。Common nonionic materials include P, OE alkyl ether, POE branched alkyl ether, POE sorbitan ester, POE glycerin fatty acid ester, POE cured castor sorbitan ester, glycerin fatty acid ester, polyglycerin fatty acid ester, etc. .
陰イオン性としては、脂肪酸、アシルグルタミン酸、ア
ルキル硫酸、アルキルリン酸、アルキルスルフォン酸の
カリウム、ナトリウム、トリエタノールアミンおよび塩
基性アミノ酸塩、POEアルキル硫酸などが一般的であ
る。Common anionic compounds include fatty acids, acylglutamic acids, alkyl sulfates, alkyl phosphoric acids, potassium, sodium, triethanolamine and basic amino acid salts of alkyl sulfonic acids, and POE alkyl sulfates.
ざらに薬剤としてビタミン類、消炎剤、殺菌剤、賦活剤
、紫外線吸収剤、ざらに、組成物を安定化きせるキレー
ト剤、緩衝剤、防腐剤などを配合しても本発明にかかる
効果を阻害するものではない。Even if vitamins, anti-inflammatory agents, bactericidal agents, activators, ultraviolet absorbers, chelating agents, buffers, preservatives, etc. that stabilize the composition are added to the grains, the effects of the present invention will be inhibited. It's not something you do.
色素、香料など、通常、組成物を修飾する成分が併用で
きることは言うまでもない。It goes without saying that ingredients that normally modify the composition, such as dyes and fragrances, can be used in combination.
次に実施例および比較例により本発明と本発明の効果に
ついて詳述するが、本発明はこれにより限定されるもの
ではない。Next, the present invention and the effects of the present invention will be explained in detail with reference to Examples and Comparative Examples, but the present invention is not limited thereto.
〈実施例1〉 美容エツセンス
ミリストイルメチルタウリン 0.1wtχナト
リウム
キトサン(分子IE120万)0.5
塩酸 0.05グリセリ
ン 10スクワラン
5防腐剤
適量精製水 全体を100とする量〈比
較例1〉 美容エツセンス
ミリストイルグルタミン酸 0.1wt%ナト
リウム
キトサン(分子量120万)0.5
塩酸 0.05グリセリ
ン 10スクワラン
5防腐剤
適量精製水 全体を100とする量く比
較例2〉 美容エツセンス
ミリストイルメチルタウリン 0.1wtXナト
リウム
グリセリン 10スクワラン
5防腐剤
適量精製水 全体を100とする
量メチルクラリン:本発明にがかるアルキロイルアルキ
ルタウリン塩型陰イオン界面活性剤
アク島グルタミン:アシルグルタミン酸塩実施例1は本
発明に従ってアルキロイルアルキルタウリン塩型陰イオ
ン界面活性剤とともに水溶性キチン誘導体を配合した例
であり、保存安定性、使用性に優れているが、これは本
発明にかかる効果である。<Example 1> Beauty essence myristoyl methyl taurine 0.1wt χ sodium chitosan (molecule IE 1.2 million) 0.5 Hydrochloric acid 0.05 Glycerin 10 Squalane
5 preservatives
Appropriate amount of purified water Amount to make the whole 100 <Comparative Example 1> Beauty essence myristoyl glutamic acid 0.1 wt% sodium chitosan (molecular weight 1.2 million) 0.5 Hydrochloric acid 0.05 Glycerin 10 Squalane
5 preservatives
Appropriate amount of purified water Weigh the total to 100 Comparative Example 2 Beauty Essence Myristoyl Methyl Taurine 0.1wtX Sodium Glycerin 10 Squalane
5 preservatives
Appropriate amount of purified water Amount to make the total 100 Methylclarin: Alkyloyl alkyl taurine salt type anionic surfactant according to the present invention Akushima glutamine: Acyl glutamate Example 1 is an alkylyl alkyl taurine salt type anionic surfactant according to the present invention This is an example in which a water-soluble chitin derivative is blended with an activator, and the product has excellent storage stability and usability, which are the effects of the present invention.
一方比較例1.2、はそれぞれ水溶性キチン誘導体とと
もに他の界面活性剤を配合した場合、および水溶性キチ
ン謂導体を配合しない例である。On the other hand, Comparative Examples 1 and 2 are examples in which a water-soluble chitin derivative and other surfactant were blended, and a case in which a water-soluble chitin derivative was not blended.
比較例1は、本発明にかかる以外の界面活性剤を水溶性
キチン誘導体とともに配合したために、経時での安定性
に劣り、実施例1の試料とともに室温下で保存した場合
析出物がある。実施例1と比較例1の保存安定性におけ
る顕著な差は本発明にかかる効果である。Comparative Example 1 contained a surfactant other than the one according to the present invention together with a water-soluble chitin derivative, so it had poor stability over time, and there was a precipitate when stored at room temperature along with the sample of Example 1. The remarkable difference in storage stability between Example 1 and Comparative Example 1 is an effect of the present invention.
一方使用性においては20名の美容技術者に実施例1と
比較例2の試料をそれぞれ使用させ使用後のしなやかざ
について問診し、しなやかさに優れた試料を選ばせたと
ころ、実施例1の試料が優れると答えた者の人数の方が
圧倒的に多かった。On the other hand, in terms of usability, 20 beauty technicians were asked to use the samples of Example 1 and Comparative Example 2 and asked about the suppleness and curls after use, and they were asked to select the sample with excellent suppleness. An overwhelmingly large number of respondents answered that the sample was excellent.
比較例2は実施例1に比較して使用性的に劣るがこれは
本発明にかかる技術を応用していないためであり、本発
明による実施例1は使用性的にも優れたものである。な
お比較例2の方が優れると答えた者についてざらに問診
したところ、肌あれが激しい状態であり、使用性の感覚
が若干麻痺している状態であったと訴えた。Comparative Example 2 is inferior in usability compared to Example 1, but this is because the technology according to the present invention is not applied, and Example 1 according to the present invention is also superior in usability. . When asked about those who answered that Comparative Example 2 was better, they complained that their skin was severely rough and their sense of use was somewhat numb.
〈実施例2〉 毛髪洗浄料
カルボキシメチルキチン 0.5wt%(分
子量1000000以上)
キトサン 0.1(分子量
1000000以上)
乳酸 0.1ヤシ油脂肪
酸メチルタウリン 30ナトリウム
プロピレングリコール 3ヤシ油ジエタノ
ールアミド 2防腐剤
適量香料 適量精製水
全体を100とする量〈比較例3〉
毛髪洗浄料
カルボキシメチルキチン 0.5wt%(分
子量1000000以上)
キトサン 0・1(分子量
1oooooo以上)
乳酸 0.1ドデシル硫
酸ナトリウム 30プロピレングリコール
3ヤシ油ジエタノールアミド 1
防腐剤 適量香料
適量精製水 全体を1
00とする量比較例3の試料を調製すべく各成分を70
℃に加熱下で混合したところ均一溶解せず二相に分離し
、使用に耐え得る毛髪洗浄材は得られなかった。これは
本発明にかかる以外の界面活性剤を利用したためである
。<Example 2> Hair cleanser Carboxymethyl chitin 0.5 wt% (molecular weight 1,000,000 or more) Chitosan 0.1 (molecular weight 1,000,000 or more) Lactic acid 0.1 Coconut oil fatty acid methyltaurine 30 Sodium propylene glycol 3 Coconut oil diethanolamide 2 Preservatives
Appropriate amount of fragrance Appropriate amount of purified water Amount to make the whole 100〈Comparative Example 3〉
Hair cleanser Carboxymethyl chitin 0.5wt% (molecular weight 1,000,000 or more) Chitosan 0.1 (molecular weight 1oooooo or more) Lactic acid 0.1 Sodium dodecyl sulfate 30 Propylene glycol
3 Coconut oil diethanolamide 1
Preservatives Appropriate amount fragrance
Appropriate amount of purified water 1 whole
To prepare the sample of Comparative Example 3, each component was reduced to 70%.
When mixed under heating at 0.degree. C., the mixture did not dissolve uniformly and separated into two phases, resulting in no usable hair cleansing material. This is because a surfactant other than the one according to the present invention was used.
これに対し実施例1では各成分を;70℃で混合すると
半透明の均一な毛髪洗浄材が得られ、撹拌冷却、室温下
2ケ月の保存後も調製直後と同様の性状を示した。これ
は本発明にしたがって水溶性キチン誘導体とともにアル
キロイルアルキルタウリン塩型陰イオン界面活性剤配合
した効果である。On the other hand, in Example 1, when each component was mixed at 70°C, a translucent and uniform hair cleansing material was obtained, and even after stirring and cooling and storage at room temperature for two months, it exhibited the same properties as immediately after preparation. This is an effect of blending the alkyl alkyl taurine salt type anionic surfactant with the water-soluble chitin derivative according to the present invention.
〈比較例4〉 毛髪洗浄材
ヤシ油脂肪酸メチルタウリン 30vtXナトリウ
ム
プロピレングリコール 3ヤシ油ジエタノ
ールアミド 2防腐剤
適量香料 適量精製水
全体を100とする量また実施例2の試
料より水溶性キチン訪導体を抜去した試料すなわち比較
例4を調製し、実施例2の試料と使用性の比較を行った
。<Comparative Example 4> Hair cleansing material Coconut oil fatty acid methyl taurine 30vtX Sodium propylene glycol 3 Coconut oil diethanolamide 2 Preservative
Appropriate amount of fragrance Appropriate amount of purified water Amount to make the whole 100 In addition, a sample in which the water-soluble chitin visiting conductor was removed from the sample of Example 2, ie, Comparative Example 4, was prepared and compared with the sample of Example 2 in terms of usability.
使用性の評価は15名の美容技術者がそれぞれの試料に
て洗髪し、乾燥前の毛髪の濡れた状態での櫛通りで判定
した。その結果15名全員が櫛通りにおいて実施例2の
試料の方が優れると答えた。これは本発明にかかる効果
である。Usability was evaluated by 15 beauty technicians who washed their hair with each sample and combed the wet hair before drying. As a result, all 15 people answered that the sample of Example 2 was superior in terms of combability. This is an effect of the present invention.
〈実施例3〉保湿クリーム
水溶性部分脱アセチルキチン 0.01vtXキト
サン(分子量220万) 0.01乳酸
0.01セチルアルコール
3ワセリン
3スクワラン 5グリセリ
ルモノステアレート 2POE (60)グリセ
リルモノ 0.1イソステアレート
ステアロイルメチルタウリン 0.5トリエタノー
ルアミン塩
バルミトイルメチルタウリン 0.5トリエタノー
ルアミン塩
グリセリン 3
プロピレングリコール 3ビタミンEアセ
テート0.5
防腐剤 適量香料
適量精製水 全体を1
00とする量〈比較例5〉保湿クリーム
水溶性部分脱アセチルキチン 0.01wt%キト
サン(分子量220万) o、oi乳酸
0.01セチルアルコール
3
ワセリン 3スクワラン
5グリセリルモノステアレート
2
POE (60)グリセリルモノ 0.1イ
ソステアレート
グリセリン 3
プロピレングリコール 3ビタミンEアセ
テート 0.5防腐剤
適量香料 適
量精製水 全体を100とする量実施例3およ
び比較例5の試料を調製後、室温下と40℃それぞれの
条件で6ケ月保存したのち、性状判定をおこなったとこ
ろ、比較例5の試料においては室温下では軟化、40℃
では分離したのに対して、実施例3の試料においては調
製直後量との間に性状の変化は観察きれなかった。すな
わち実施例3の試料は経時安定性に優れるものであるが
、これは本発明にかかる効果である。<Example 3> Moisturizing cream Water-soluble partially deacetylated chitin 0.01vtX chitosan (molecular weight 2.2 million) 0.01 lactic acid
0.01 Cetyl Alcohol 3 Vaseline
3 Squalane 5 Glyceryl Monostearate 2 POE (60) Glyceryl Mono 0.1 Isostearate Stearoyl Methyl Taurine 0.5 Triethanolamine Salt Balmitoyl Methyl Taurine 0.5 Triethanolamine Salt Glycerin 3 Propylene Glycol 3 Vitamin E Acetate 0 .5 Preservatives Appropriate amount of fragrance
Appropriate amount of purified water 1 whole
Amount to be 00 (Comparative Example 5) Moisturizing cream Water-soluble partially deacetylated chitin 0.01wt% chitosan (molecular weight 2.2 million) o, oi lactic acid
0.01 Cetyl Alcohol 3 Vaseline 3 Squalane
5 Glyceryl Monostearate
2 POE (60) Glyceryl mono 0.1 Isostearate glycerin 3 Propylene glycol 3 Vitamin E acetate 0.5 Preservative
Appropriate amount of fragrance Appropriate amount of purified water Amount to make the whole amount 100 After preparing the samples of Example 3 and Comparative Example 5, they were stored at room temperature and 40°C for 6 months, and their properties were evaluated. The sample softens at room temperature, 40℃
In contrast, in the sample of Example 3, no change in properties could be observed between the amount immediately after preparation and the amount immediately after preparation. That is, the sample of Example 3 has excellent stability over time, which is an effect of the present invention.
〈実施例4〉 ボディクレンザ−
ラウロイルメチルタウリン 10vt駕ナト
リウム
POE (60)硬化ヒマシ油 1ヤ
シ油ジエタノールアミド 2キチンサルフ
エート 10(分子量200000)
グリセリン 5プロピレング
リコール 2防腐剤
適量香料
適量精製水 全体を100とする量〈比較
例6〉 ボディクレンザ−
ラウロイルメチルタウリン 10vtXナト
リウム
POE (60)硬化ヒマシ油 1ヤ
シ油ジエタノールアミド 2グリセリン
5プロピレングリコール
2防腐剤 適量
香料 適量精製水
全体を100とする量実施例4と比較例6の試
料を20名の美容技術者に使用させ、使用後の肌のなめ
らかざ、かきつきについて10点法で評価させたところ
、平均値は下表の通りであった。<Example 4> Body cleanser - Lauroyl methyl taurine 10vt Sodium POE (60) Hydrogenated castor oil 1 Coconut oil diethanolamide 2 Chitin sulfate 10 (molecular weight 200,000) Glycerin 5 Propylene glycol 2 Preservative
Appropriate amount of fragrance
Appropriate amount of purified water Amount to make the whole 100 <Comparative Example 6> Body cleanser - Lauroyl methyl taurine 10vtX sodium POE (60) Hydrogenated castor oil 1 Coconut oil diethanolamide 2 Glycerin
5 propylene glycol
2 Preservatives Appropriate amount Flavoring Appropriate amount Purified water
When 20 beauty technicians used the samples of Example 4 and Comparative Example 6 and evaluated the smoothness and roughness of the skin after use using a 10-point scale, the average value was lower. It was as shown in the table.
なめらかである 10点 なめらかでない 1点 かきつかない 10点 かきつく 1点 表−2 この評点の差はあきらかに本発明にかかる効果である。Smooth 10 points Not smooth 1 point No scratches 10 points Striking 1 point Table-2 This difference in scores is clearly an effect of the present invention.
〈実施例5〉洗顔ローション
ラウロイルメチルタウリン 0.05wtXナ
トリウム
水溶性部分脱アセチルキチン 0.01(分子量
150万以上)
酢酸 0.0195%エ
タノール 15グリセリン
5
防腐剤 適量精製水
全体を100とする量実施例5の洗顔ローショ
ンは使用性、安定性に優れるものであった。<Example 5> Facial cleansing lotion lauroyl methyl taurine 0.05wtX sodium water-soluble partially deacetyl chitin 0.01 (molecular weight 1.5 million or more) acetic acid 0.0195% ethanol 15 glycerin
5 Preservatives Appropriate amount of purified water
The face wash lotion of Example 5 was excellent in usability and stability.
〈実施例6〉水溶性ポマード
水溶性部分脱アセチルキチン 1 、 Ovt%(
分子量180万以上)
乳酸 0.5ミリストイル
メチルタウリン 1.0カリウム
低粘度シリコン油(6cs) 5ジプロピレ
ングリコール 5
グリセリン 25
ポリビニルピロリドン 0.3防腐剤
適量
精製水 全体をiooとする量実施例6の試料
は使用性、安定性に優れるものであった。<Example 6> Water-soluble pomade Water-soluble partially deacetylated chitin 1, Ovt% (
Molecular weight 1.8 million or more) Lactic acid 0.5 Myristoylmethyltaurine 1.0 Potassium Low viscosity silicone oil (6cs) 5 Dipropylene glycol 5 Glycerin 25 Polyvinylpyrrolidone 0.3 Preservative
Appropriate amount of purified water (total ioo) The sample of Example 6 was excellent in usability and stability.
〈実施例7〉 マツサージングクリームカルボキシメチ
ルキチン 0.2wt%(分子量600000
〜800000)グライコールキチン
0.2(分子量120000〜300000)ヤシ油脂
肪酸メチルタウリン 0.5トリエタノールアミン
流動パラフィン 5
低粘度シリコン(6cs) 5揮発性環伏シ
リコン 5
ホホバ油 5
ソルビトール液 10グリセリン
10
メチルセルロース 0.5防腐剤
適量精製水 全体を10
0とする量実施例7の試料は使用性、安定性に優れるも
のであった。<Example 7> Pine surging cream carboxymethyl chitin 0.2 wt% (molecular weight 600,000
~800000) Glycol chitin
0.2 (molecular weight 120,000-300,000) Coconut oil fatty acid methyltaurine 0.5 Triethanolamine liquid paraffin 5 Low viscosity silicone (6cs) 5 Volatile cyclic silicone 5 Jojoba oil 5 Sorbitol liquid 10 Glycerin
10 Methylcellulose 0.5 Preservative
Appropriate amount of purified water, total 10
The sample of Example 7 was excellent in usability and stability.
〈実施例8〉クレンジングペースト
低分子化キトサン 5wt%(平均分子
量10000)
ラウロイルメチルタウリン 20
ナトリウム
ミリストイルメチルタウリン 10
ナトリウム
ステアロイルタウリン 5
ナトリウム
ポリエチレングリコール400 10香料
適量防腐剤
適量
精製水 全体を100とする量
実施例8の試料は使用性、安定性に優れるものであった
。<Example 8> Cleansing paste Low molecular chitosan 5 wt% (average molecular weight 10000) Lauroyl methyl taurine 20 Sodium myristoyl methyl taurine 10 Sodium stearoyl taurine 5 Sodium polyethylene glycol 400 10 Fragrance
Appropriate amount of preservative
Appropriate amount of purified water (total amount being 100) The sample of Example 8 was excellent in usability and stability.
Claims (1)
基または、アルケニル基、R_2は平均炭素原子数1な
いし3の低級アルキル基、Mはアルカリ金属、有機アミ
ン類、塩基性アミノ酸類を表す。)で表されるアルキロ
イルアルキルタウリン塩型陰イオン界面活性剤の一種ま
たは二種以上と、水溶性キチン誘導体の一種または二種
以上を配合したことを特徴とする皮膚および毛髪用組成
物。[Claims] General formula ▲ Numerical formula, chemical formula, table, etc. group, M represents an alkali metal, organic amines, basic amino acids) and one or more water-soluble chitin derivatives. A composition for skin and hair, characterized in that it contains at least one species.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP11402987A JPH0696489B2 (en) | 1987-05-11 | 1987-05-11 | Compositions for skin and hair |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP11402987A JPH0696489B2 (en) | 1987-05-11 | 1987-05-11 | Compositions for skin and hair |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS63277608A true JPS63277608A (en) | 1988-11-15 |
JPH0696489B2 JPH0696489B2 (en) | 1994-11-30 |
Family
ID=14627255
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP11402987A Expired - Lifetime JPH0696489B2 (en) | 1987-05-11 | 1987-05-11 | Compositions for skin and hair |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0696489B2 (en) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0636686A1 (en) * | 1993-07-28 | 1995-02-01 | L'oreal | Washing composition for keratin fibres based on chitosan derived polymers |
EP0795316A1 (en) * | 1996-02-14 | 1997-09-17 | Henkel Kommanditgesellschaft auf Aktien | Cosmetic and pharmaceutical emulsions comprising partial glyceride (ether) sulphate, emulsifiers and chitosan |
AU720008B2 (en) * | 1996-12-16 | 2000-05-18 | Noviscens Ab | Medical composition and use thereof for the manufacture of topical barrier formulation, a UV-radiation absorbing formulation, or an antiviral, antifungal, or antiinflammatory formulation |
WO2006029453A1 (en) * | 2004-09-14 | 2006-03-23 | Ip Organisers | Acylated saccharides and process for production thereof |
JP2019043853A (en) * | 2017-08-30 | 2019-03-22 | 旭化成株式会社 | Percutaneous absorption promoter, percutaneous absorption promoting auxiliary, and percutaneous pharmaceutical preparation |
-
1987
- 1987-05-11 JP JP11402987A patent/JPH0696489B2/en not_active Expired - Lifetime
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0636686A1 (en) * | 1993-07-28 | 1995-02-01 | L'oreal | Washing composition for keratin fibres based on chitosan derived polymers |
FR2708276A1 (en) * | 1993-07-28 | 1995-02-03 | Oreal | Washing composition for keratin fibers based on polymers derived from chitosan. |
US5571458A (en) * | 1993-07-28 | 1996-11-05 | L'oreal | Washing composition for keratin fibres which is based on chitosan-derived polymers |
EP0795316A1 (en) * | 1996-02-14 | 1997-09-17 | Henkel Kommanditgesellschaft auf Aktien | Cosmetic and pharmaceutical emulsions comprising partial glyceride (ether) sulphate, emulsifiers and chitosan |
AU720008B2 (en) * | 1996-12-16 | 2000-05-18 | Noviscens Ab | Medical composition and use thereof for the manufacture of topical barrier formulation, a UV-radiation absorbing formulation, or an antiviral, antifungal, or antiinflammatory formulation |
WO2006029453A1 (en) * | 2004-09-14 | 2006-03-23 | Ip Organisers | Acylated saccharides and process for production thereof |
WO2006029452A1 (en) * | 2004-09-14 | 2006-03-23 | Ip Organisers Pty Ltd | Acylated saccharides and uses thereof |
JP2019043853A (en) * | 2017-08-30 | 2019-03-22 | 旭化成株式会社 | Percutaneous absorption promoter, percutaneous absorption promoting auxiliary, and percutaneous pharmaceutical preparation |
Also Published As
Publication number | Publication date |
---|---|
JPH0696489B2 (en) | 1994-11-30 |
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