JPH01146816A - Skin cleaning agent composition and production thereof - Google Patents
Skin cleaning agent composition and production thereofInfo
- Publication number
- JPH01146816A JPH01146816A JP30462987A JP30462987A JPH01146816A JP H01146816 A JPH01146816 A JP H01146816A JP 30462987 A JP30462987 A JP 30462987A JP 30462987 A JP30462987 A JP 30462987A JP H01146816 A JPH01146816 A JP H01146816A
- Authority
- JP
- Japan
- Prior art keywords
- acidic amino
- acyl acidic
- amino acid
- weight
- skin
- 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
- 238000004519 manufacturing process Methods 0.000 title claims description 4
- 239000012459 cleaning agent Substances 0.000 title abstract description 6
- 150000001413 amino acids Chemical class 0.000 claims abstract description 48
- 230000002378 acidificating effect Effects 0.000 claims abstract description 47
- -1 amine salt Chemical class 0.000 claims abstract description 43
- 150000003839 salts Chemical class 0.000 claims abstract description 21
- 238000010438 heat treatment Methods 0.000 claims abstract description 8
- 239000006071 cream Substances 0.000 claims description 16
- 229910052783 alkali metal Inorganic materials 0.000 claims description 14
- 229910052751 metal Inorganic materials 0.000 claims description 11
- 239000002184 metal Substances 0.000 claims description 11
- 238000003756 stirring Methods 0.000 claims description 9
- 239000012736 aqueous medium Substances 0.000 claims description 8
- 150000002736 metal compounds Chemical class 0.000 claims description 8
- 239000004615 ingredient Substances 0.000 claims description 7
- 150000007524 organic acids Chemical class 0.000 claims description 7
- 150000001875 compounds Chemical class 0.000 claims description 6
- 230000015572 biosynthetic process Effects 0.000 claims description 4
- 229920000728 polyester Polymers 0.000 claims 1
- 125000002924 primary amino group Chemical class [H]N([H])* 0.000 claims 1
- 230000014759 maintenance of location Effects 0.000 abstract description 11
- 238000002156 mixing Methods 0.000 abstract description 5
- 230000035945 sensitivity Effects 0.000 abstract description 3
- 208000017520 skin disease Diseases 0.000 abstract description 3
- 239000006185 dispersion Substances 0.000 abstract description 2
- 239000003995 emulsifying agent Substances 0.000 abstract description 2
- 230000007794 irritation Effects 0.000 abstract description 2
- 239000000126 substance Substances 0.000 abstract description 2
- 238000005406 washing Methods 0.000 abstract description 2
- 239000000080 wetting agent Substances 0.000 abstract description 2
- 239000003513 alkali Substances 0.000 abstract 2
- 235000001014 amino acid Nutrition 0.000 description 34
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 15
- 239000002253 acid Substances 0.000 description 13
- 239000003599 detergent Substances 0.000 description 13
- 230000000704 physical effect Effects 0.000 description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
- VBICKXHEKHSIBG-UHFFFAOYSA-N 1-monostearoylglycerol Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(O)CO VBICKXHEKHSIBG-UHFFFAOYSA-N 0.000 description 6
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 6
- 235000014113 dietary fatty acids Nutrition 0.000 description 6
- 239000000194 fatty acid Substances 0.000 description 6
- 229930195729 fatty acid Natural products 0.000 description 6
- 239000008213 purified water Substances 0.000 description 6
- 239000004094 surface-active agent Substances 0.000 description 6
- 238000000034 method Methods 0.000 description 5
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 4
- 235000019441 ethanol Nutrition 0.000 description 4
- 150000004665 fatty acids Chemical class 0.000 description 4
- IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 4
- 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 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- 239000002202 Polyethylene glycol Substances 0.000 description 3
- KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 3
- 150000007513 acids Chemical class 0.000 description 3
- 239000004359 castor oil Substances 0.000 description 3
- 235000019438 castor oil Nutrition 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical class OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- 239000006260 foam Substances 0.000 description 3
- 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 3
- 230000000774 hypoallergenic effect Effects 0.000 description 3
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 3
- 235000019341 magnesium sulphate Nutrition 0.000 description 3
- 229920001223 polyethylene glycol Polymers 0.000 description 3
- 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
- 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 2
- RGHNJXZEOKUKBD-SQOUGZDYSA-N D-gluconic acid Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C(O)=O RGHNJXZEOKUKBD-SQOUGZDYSA-N 0.000 description 2
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
- WHUUTDBJXJRKMK-UHFFFAOYSA-N Glutamic acid Natural products OC(=O)C(N)CCC(O)=O WHUUTDBJXJRKMK-UHFFFAOYSA-N 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Chemical compound NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 description 2
- WHUUTDBJXJRKMK-VKHMYHEASA-N L-glutamic acid Chemical compound OC(=O)[C@@H](N)CCC(O)=O WHUUTDBJXJRKMK-VKHMYHEASA-N 0.000 description 2
- 239000005639 Lauric acid Substances 0.000 description 2
- TWRXJAOTZQYOKJ-UHFFFAOYSA-L Magnesium chloride Chemical compound [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 description 2
- 235000021314 Palmitic acid Nutrition 0.000 description 2
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 2
- 125000002252 acyl group Chemical group 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- SXBBFOVRSQCYFE-SQKCAUCHSA-L disodium;(2s)-2-(tetradecanoylamino)pentanedioate Chemical compound [Na+].[Na+].CCCCCCCCCCCCCC(=O)N[C@H](C([O-])=O)CCC([O-])=O SXBBFOVRSQCYFE-SQKCAUCHSA-L 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000003205 fragrance Substances 0.000 description 2
- 239000004220 glutamic acid Substances 0.000 description 2
- 235000013922 glutamic acid Nutrition 0.000 description 2
- 229940075507 glyceryl monostearate Drugs 0.000 description 2
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 2
- 239000001788 mono and diglycerides of fatty acids Substances 0.000 description 2
- WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 2
- 235000005985 organic acids Nutrition 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 239000000600 sorbitol Substances 0.000 description 2
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 2
- JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 description 2
- AVBJHQDHVYGQLS-AWEZNQCLSA-N (2s)-2-(dodecanoylamino)pentanedioic acid Chemical compound CCCCCCCCCCCC(=O)N[C@H](C(O)=O)CCC(O)=O AVBJHQDHVYGQLS-AWEZNQCLSA-N 0.000 description 1
- BJEPYKJPYRNKOW-REOHCLBHSA-N (S)-malic acid Chemical compound OC(=O)[C@@H](O)CC(O)=O BJEPYKJPYRNKOW-REOHCLBHSA-N 0.000 description 1
- RZRNAYUHWVFMIP-KTKRTIGZSA-N 1-oleoylglycerol Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCC(O)CO RZRNAYUHWVFMIP-KTKRTIGZSA-N 0.000 description 1
- IIZPXYDJLKNOIY-JXPKJXOSSA-N 1-palmitoyl-2-arachidonoyl-sn-glycero-3-phosphocholine Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCC\C=C/C\C=C/C\C=C/C\C=C/CCCCC IIZPXYDJLKNOIY-JXPKJXOSSA-N 0.000 description 1
- MLOYYKYQLFOZOE-UHFFFAOYSA-N 2-(tetradecanoylamino)butanedioic acid Chemical compound CCCCCCCCCCCCCC(=O)NC(C(O)=O)CC(O)=O MLOYYKYQLFOZOE-UHFFFAOYSA-N 0.000 description 1
- ODHCTXKNWHHXJC-VKHMYHEASA-N 5-oxo-L-proline Chemical compound OC(=O)[C@@H]1CCC(=O)N1 ODHCTXKNWHHXJC-VKHMYHEASA-N 0.000 description 1
- 239000004135 Bone phosphate Chemical class 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 1
- RGHNJXZEOKUKBD-UHFFFAOYSA-N D-gluconic acid Natural products OCC(O)C(O)C(O)C(O)C(O)=O RGHNJXZEOKUKBD-UHFFFAOYSA-N 0.000 description 1
- ODBLHEXUDAPZAU-ZAFYKAAXSA-N D-threo-isocitric acid Chemical class OC(=O)[C@H](O)[C@@H](C(O)=O)CC(O)=O ODBLHEXUDAPZAU-ZAFYKAAXSA-N 0.000 description 1
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 1
- 239000004471 Glycine Substances 0.000 description 1
- ODBLHEXUDAPZAU-FONMRSAGSA-N Isocitric acid Chemical class OC(=O)[C@@H](O)[C@H](C(O)=O)CC(O)=O ODBLHEXUDAPZAU-FONMRSAGSA-N 0.000 description 1
- CKLJMWTZIZZHCS-REOHCLBHSA-N L-aspartic acid Chemical compound OC(=O)[C@@H](N)CC(O)=O CKLJMWTZIZZHCS-REOHCLBHSA-N 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- ATFFFUXLAJBBDE-FQEVSTJZSA-N N-Stearoyl glutamic acid Chemical compound CCCCCCCCCCCCCCCCCC(=O)N[C@H](C(O)=O)CCC(O)=O ATFFFUXLAJBBDE-FQEVSTJZSA-N 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 241000282320 Panthera leo Species 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- 235000004443 Ricinus communis Nutrition 0.000 description 1
- 206010040880 Skin irritation Diseases 0.000 description 1
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 235000011054 acetic acid Nutrition 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000001447 alkali salts Chemical group 0.000 description 1
- BJEPYKJPYRNKOW-UHFFFAOYSA-N alpha-hydroxysuccinic acid Natural products OC(=O)C(O)CC(O)=O BJEPYKJPYRNKOW-UHFFFAOYSA-N 0.000 description 1
- AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical class [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- DIZPMCHEQGEION-UHFFFAOYSA-H aluminium sulfate (anhydrous) Chemical compound [Al+3].[Al+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O DIZPMCHEQGEION-UHFFFAOYSA-H 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 239000002280 amphoteric surfactant Substances 0.000 description 1
- 150000001450 anions Chemical group 0.000 description 1
- 239000002260 anti-inflammatory agent Substances 0.000 description 1
- 229940121363 anti-inflammatory agent Drugs 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 235000003704 aspartic acid Nutrition 0.000 description 1
- 229910052788 barium Inorganic materials 0.000 description 1
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 1
- 159000000009 barium salts Chemical class 0.000 description 1
- 229910052790 beryllium Inorganic materials 0.000 description 1
- ATBAMAFKBVZNFJ-UHFFFAOYSA-N beryllium atom Chemical compound [Be] ATBAMAFKBVZNFJ-UHFFFAOYSA-N 0.000 description 1
- 159000000004 beryllium salts Chemical class 0.000 description 1
- OQFSQFPPLPISGP-UHFFFAOYSA-N beta-carboxyaspartic acid Natural products OC(=O)C(N)C(C(O)=O)C(O)=O OQFSQFPPLPISGP-UHFFFAOYSA-N 0.000 description 1
- KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 239000001110 calcium chloride Substances 0.000 description 1
- 229910001628 calcium chloride Inorganic materials 0.000 description 1
- 159000000007 calcium salts Chemical class 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 239000002738 chelating agent Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 239000003240 coconut oil Substances 0.000 description 1
- 235000019864 coconut oil Nutrition 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 239000000645 desinfectant Substances 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 238000002845 discoloration Methods 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 238000005187 foaming Methods 0.000 description 1
- 239000001530 fumaric acid Substances 0.000 description 1
- 239000000174 gluconic acid Substances 0.000 description 1
- 235000012208 gluconic acid Nutrition 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 239000003906 humectant Substances 0.000 description 1
- 150000004679 hydroxides Chemical class 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 239000004310 lactic acid Substances 0.000 description 1
- 235000014655 lactic acid Nutrition 0.000 description 1
- 125000000400 lauroyl 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])[H] 0.000 description 1
- 239000000787 lecithin Substances 0.000 description 1
- 235000010445 lecithin Nutrition 0.000 description 1
- 229940067606 lecithin Drugs 0.000 description 1
- 229910003002 lithium salt Inorganic materials 0.000 description 1
- 159000000002 lithium salts Chemical class 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910001629 magnesium chloride Inorganic materials 0.000 description 1
- 159000000003 magnesium salts Chemical class 0.000 description 1
- 239000002075 main ingredient Substances 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- 239000001630 malic acid Substances 0.000 description 1
- 235000011090 malic acid Nutrition 0.000 description 1
- 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 1
- 150000002823 nitrates Chemical class 0.000 description 1
- MGFYIUFZLHCRTH-UHFFFAOYSA-N nitrilotriacetic acid Chemical compound OC(=O)CN(CC(O)=O)CC(O)=O MGFYIUFZLHCRTH-UHFFFAOYSA-N 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 125000002811 oleoyl 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])=C([H])\C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-N phosphoric acid Substances OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229940068918 polyethylene glycol 400 Drugs 0.000 description 1
- 229920001282 polysaccharide Polymers 0.000 description 1
- 239000005017 polysaccharide Substances 0.000 description 1
- 159000000001 potassium salts Chemical class 0.000 description 1
- 229940079889 pyrrolidonecarboxylic acid Drugs 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 230000001953 sensory effect Effects 0.000 description 1
- 230000036556 skin irritation Effects 0.000 description 1
- 231100000475 skin irritation Toxicity 0.000 description 1
- 229940077092 sodium myristoyl glutamate Drugs 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 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 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
- 239000002904 solvent Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000001384 succinic acid Substances 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- TUNFSRHWOTWDNC-HKGQFRNVSA-N tetradecanoic acid Chemical compound CCCCCCCCCCCCC[14C](O)=O TUNFSRHWOTWDNC-HKGQFRNVSA-N 0.000 description 1
- ODBLHEXUDAPZAU-UHFFFAOYSA-N threo-D-isocitric acid Chemical class OC(=O)C(O)C(C(O)=O)CC(O)=O ODBLHEXUDAPZAU-UHFFFAOYSA-N 0.000 description 1
- 150000003751 zinc Chemical class 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 239000011592 zinc chloride Substances 0.000 description 1
- 235000005074 zinc chloride Nutrition 0.000 description 1
Landscapes
- Cosmetics (AREA)
- Detergent Compositions (AREA)
Abstract
Description
【発明の詳細な説明】
産業上の利用分野
本発明は、皮膚に対する刺激が少なく、すすぎ性が良好
な上K、高温での粘度安定性、クリーム状態の保形性が
優れたクリーム状皮膚洗浄剤組成物及び・その製造方法
に関するものである。DETAILED DESCRIPTION OF THE INVENTION Field of Industrial Application The present invention provides a cream-like skin cleanser that is less irritating to the skin, has good rinsability, and has excellent viscosity stability at high temperatures and cream-like shape retention. The present invention relates to a drug composition and a method for producing the same.
従来の技術
N−アシル酸性アミノ酸系界面活性剤を主成分とした洗
浄剤は公知であシ、皮膚に対する刺激性が低く、優れた
洗浄力を有するために、−絞入用としてだけでなく、皮
膚敏感症の人や、皮膚病患者の間でも広く用いられてい
る。BACKGROUND OF THE INVENTION Cleaning agents based on N-acyl acidic amino acid surfactants are known, and because they are less irritating to the skin and have excellent cleaning power, they can be used not only for squeezing, but also for squeezing. It is also widely used by people with skin sensitivities and patients with skin diseases.
このように、N−アシル酸性アミノ酸系界面活性剤は、
皮膚に対しては穏やかな作用を示し、安全に使用できる
反面、泡のクリーミイ性が低く滑らかな使用感が得られ
ないとか、すすぎ時にいつまでもぬるぬるした感じが残
シ、さつばシした感触が得られないという欠点を有して
いる。In this way, the N-acyl acidic amino acid surfactant is
Although it has a mild effect on the skin and is safe to use, the foam is not creamy enough to provide a smooth feeling of use, and when rinsed, it leaves a sticky feeling or leaves a sticky feeling. It has the disadvantage that it cannot be used.
このようなN−アシル酸性アミノ酸系界面活性剤の欠点
を改善するために1両性界面活性剤を添加したもの(特
開昭48−56205号公報、特開昭18−56708
号公報)、レシチンを添加したもの(特開昭50−70
410号公報)、アルキルリン酸エステル塩を添加した
もの(特開昭54−120610号公報)、カチオン化
多糖類を添加したもの(特開昭55−65298号公報
)、高級脂肪酸を添加したもの(特開昭56−1069
99号公報)などが提案されているが、これらのものに
おいても、泡の感触が若干改善されるだけで、すすぎ性
については十分満足しうる結果は得られていない。In order to improve the drawbacks of such N-acyl acidic amino acid surfactants, amphoteric surfactants have been added (JP-A-48-56205, JP-A-18-56708).
(Japanese Patent Application Laid-Open No. 1983-1987), with lecithin added
410), those to which alkyl phosphate ester salts are added (JP-A-54-120610), cationic polysaccharides (JP-A-55-65298), and higher fatty acids. (Unexamined Japanese Patent Publication No. 56-1069
No. 99) and the like have been proposed, but even with these, the feel of the foam is only slightly improved, but satisfactory results have not been obtained in terms of rinsability.
他方、市販品の中には、大量の脂肪酸アルカリ塩を配合
して、泡の感触やすすぎ性を改善したものもあるが、こ
のように大量の脂肪酸アルカリ塩を配合すると、N−ア
シル酸性アミノ酸系界面活性剤が本来有している低刺激
性がそこなわれるのを免れない。On the other hand, some commercially available products contain a large amount of fatty acid alkali salts to improve the foam feel and rinsability. The inherent hypoallergenic properties of surfactants are inevitably impaired.
さらに、最近N−アシル酸性アミノ酸の一価金属塩の一
部を多価金属塩に変えることによシ使用感を向上させた
皮膚洗浄剤が提案されているが。Furthermore, recently, a skin cleansing agent has been proposed in which a part of the monovalent metal salt of the N-acyl acidic amino acid is changed to a polyvalent metal salt, thereby improving the feeling of use.
このものについても前記したすすぎ性についての問題が
残っている上に、溶解度の温度依存性が大きいために、
比較的高い周囲温度に置くと、この中に含まれるN−ア
シルアミノ酸系界面活性剤の溶解度が変化し、洗浄剤組
成物の粘度安定性やクリーム状態での保形性が低下する
という欠点がある。This product still has the problem of rinsability mentioned above, and its solubility is highly dependent on temperature, so
When placed at a relatively high ambient temperature, the solubility of the N-acylamino acid surfactant contained therein changes, resulting in a decrease in the viscosity stability and shape retention of the detergent composition in cream form. be.
発明が解決しようとする問題点
本発明は、従来のN−アシル酸性アミノ酸塩を主成分と
するクリーム状皮膚洗浄剤がもつ低刺激性や良好な使用
感をそこなうことなく、そのすすぎ性及び高温における
粘度安定性及び保形性を改善することを目的としてなさ
れたものである。Problems to be Solved by the Invention The present invention aims to improve the rinsability and high temperature properties of conventional cream skin cleansers containing N-acyl acidic amino acid salts without sacrificing their hypoallergenic properties and good feeling of use. This was done with the aim of improving the viscosity stability and shape retention of.
問題点を解決するための手段
本発明者らは、皮膚に対する刺激性が低く、かつすすぎ
時におけるぬめ多感の除去を迅速に行える上に、夏期の
高温時、熱帯、亜熱帯の高温地域においても優れた粘度
安定性及び保形性を示すクリーム状皮膚洗浄剤を開発す
るために、鋭意研究を重ねた結果、N−アシル酸性アミ
ノ酸のアルカリ金属塩又は有機アミン塩と、N−アシル
酸性アミノ酸の多価金属塩と、N−アシル酸性アミノ酸
とを特足の割合で混合した界面活性剤を含有するクリー
ム状組成物とすることによシその目的を達成しうろこと
、及びこのクリーム状組成物は、クリーム形成に必要な
成分を含む水性媒質中にN −アシル酸性アミノ酸のア
ルカリ塩又は有機。アミン塩を溶解し、これに所要量の
水溶性多価金属化合物及び有機酸を加え反応させること
によシ容易に製造しうろことを見出し、この知見に基づ
いて本発明をなすに至った。Means for Solving the Problems The present inventors have developed a method that has low irritation to the skin, can quickly remove slimy skin during rinsing, and can be used in high temperatures in summer, in tropical and subtropical regions. In order to develop a creamy skin cleansing agent that exhibits excellent viscosity stability and shape retention, we have conducted intensive research to develop a creamy skin cleansing agent that exhibits excellent viscosity stability and shape retention. This objective is achieved by creating a cream composition containing a surfactant in which a polyvalent metal salt of 1, and an N-acyl acidic amino acid are mixed in a particular ratio. The product is an alkali salt of an N-acyl acidic amino acid or an organic compound in an aqueous medium containing the ingredients necessary for cream formation. It was discovered that it can be easily produced by dissolving an amine salt, adding a required amount of a water-soluble polyvalent metal compound and an organic acid thereto, and causing the reaction. Based on this knowledge, the present invention was accomplished.
すなわち、本発明は、(a) N−アシル酸性アミノ酸
のアルカリ金属塩及び有機アミン塩の中から選ばれた少
なくとも1種の成分30〜65重量%、(b) N−ア
シル酸性アミノ酸の多価金属塩の中から選ばれた少なく
とも1種の成分5〜40重量係及び(c) N−アシル
酸性アミノ酸の中から選ばれた少なくとも1種の成分1
5〜40重量係から成るN−アシル酸性アミノ酸系混合
物を、組成物全量に基づき15〜40重量係含有したこ
とを特徴とするクリーム状皮膚洗浄剤組成物及びこのも
のをクリーム形成に必要な成分を含む水性媒質中に、所
要量のN−アシル酸性アミノ酸のアルカリ金属塩及び有
機アミン塩の中から選ばれた少なくとも1種の化合物を
溶解し、これに所要ftQ水溶性多価金属化合物及び有
機酸を加え、かきまぜながら加熱反応させることによシ
製造する方法を提供するものである。That is, the present invention provides (a) 30 to 65% by weight of at least one component selected from alkali metal salts and organic amine salts of N-acyl acidic amino acids, (b) polyvalent N-acyl acidic amino acids. (c) At least one component selected from metal salts (5 to 40% by weight) and (c) at least one component selected from N-acyl acidic amino acids (1)
A creamy skin cleansing composition characterized by containing an N-acyl acidic amino acid mixture of 5 to 40% by weight based on the total amount of the composition, and this composition as an ingredient necessary for cream formation. A required amount of at least one compound selected from an alkali metal salt and an organic amine salt of an N-acyl acidic amino acid is dissolved in an aqueous medium containing a required amount of ftQ water-soluble polyvalent metal compound and an organic amine salt. This provides a method for producing by adding an acid and causing a heating reaction while stirring.
本発明のN−アシル酸性アミノ酸系混合物中の(a)成
分及び(’b)成分の塩の陰イオン部分を構成するN−
アシル酸性アミノ酸及び(C)成分として用いるN−ア
シル酸性アミノ酸は、従来低刺激性の皮膚洗浄剤の主成
分として用いられているものと同じものでよく、これら
の中から任意に選択することができる。このようなもの
としては、酸性アミノ酸すなわち1個のアミノ基と2個
以上のカルボキシル基をもつアミノ酸、例えばグルタミ
ン酸、アスパラギン酸、システィン酸、ホモシスティン
酸などのアミノ酸のアミノ基窒素原子が炭素数8〜24
の長鎖アシル基、例えばラウロイル基、バルミトイル基
、ミリストイル基、オレオイル基、ココイル基などによ
シ置換されている化合物、例えばN−ラウロイルグルタ
ミン酸、N−ミリストイルグルタミン酸、N−バルミト
イルグルタミン酸、N−ステアロイルグルタミン酸、N
−ラウロイルシスティン酸、N−ミリストイルアスパラ
ギン酸、N−ラウロイルシスティン酸、N−バルミトイ
ルホモシスティン酸などを挙げることがでキル。The N- constituting the anion moiety of the salt of component (a) and component ('b) in the N-acyl acidic amino acid mixture of the present invention
The acyl acidic amino acids and the N-acyl acidic amino acids used as component (C) may be the same as those conventionally used as the main ingredients of hypoallergenic skin cleansers, and may be arbitrarily selected from these. can. Such amino acids include acidic amino acids, that is, amino acids having one amino group and two or more carboxyl groups, such as glutamic acid, aspartic acid, cystic acid, and homocystic acid, where the amino group nitrogen atom has 8 carbon atoms. ~24
compounds substituted with long-chain acyl groups such as lauroyl, valmitoyl, myristoyl, oleoyl, cocoyl, etc., such as N-lauroylglutamic acid, N-myristoylglutamic acid, N-balmitoylglutamic acid, N-stearoylglutamic acid, N
-Lauroyl cystic acid, N-myristoyl aspartic acid, N-lauroyl cystic acid, N-balmitoyl homocystic acid, etc. can be mentioned.
本発明の(α)成分としては、これらのN−アシル酸性
アミノ酸のアルカリ金属塩及び有機アミン塩が用いられ
るが、このアルカリ金属塩には、ナトリウム塩、カリウ
ム塩、リチウム塩など、また有機アミン塩には、低級ア
ルキルアミン塩、アルカノールアミン塩、塩基性アミノ
酸塩などが包含される。これらのアルカリ金属塩や有機
アミン塩は、単独で用いてもよいし、2種以上の混合物
として用いてもよい。As the component (α) of the present invention, alkali metal salts and organic amine salts of these N-acyl acidic amino acids are used, and these alkali metal salts include sodium salts, potassium salts, lithium salts, etc. Salts include lower alkylamine salts, alkanolamine salts, basic amino acid salts, and the like. These alkali metal salts and organic amine salts may be used alone or as a mixture of two or more.
また、(b)成分としては、これらのN−アシル酸性ア
ミノ酸の多価金属塩が用いられるが、この多価金属塩に
は、ベリリウム塩、マグネシウム塩、カルシウム塩、バ
リウム塩、亜鉛塩、アルミニウム塩などが包含される。In addition, as component (b), polyvalent metal salts of these N-acyl acidic amino acids are used, and these polyvalent metal salts include beryllium salts, magnesium salts, calcium salts, barium salts, zinc salts, and aluminum salts. Includes salt, etc.
これらの多価金属塩は単独で用いてもよいし、また2種
以上の混合物として用いてもよい。These polyvalent metal salts may be used alone or as a mixture of two or more.
次に本発明組成物中のN−アシル酸性アミノ酸系混合物
は、(a)成分30〜65重量係、(b)成分5〜40
重量係及び(C)成分15〜40重量係の組成比を有す
ることが必要である。この(a)成分が65重重量上シ
も多くなると、すすぎ時のぬめシの迅速な消失ができな
くなり、また高温における保形性が低下するし、この(
a)成分が30重量係未満になると、皮膚刺激性の低い
洗浄剤を得ることができない。Next, the N-acyl acidic amino acid mixture in the composition of the present invention contains (a) component 30 to 65% by weight, and (b) component 5 to 40% by weight.
It is necessary to have a composition ratio of 15 to 40% by weight of component (C). If this (a) component exceeds 65% by weight, the slime will not disappear quickly during rinsing, and the shape retention at high temperatures will decrease.
If the content of a) component is less than 30% by weight, a detergent with low skin irritation cannot be obtained.
また、(b)成分や(C)成分が40重重量上シも多く
なると、洗浄力、起泡力が低下するし、(b)成分が5
重量チ未満になったシ(C)成分が15重量係未満にな
ると高温における粘度安定性や保形性の改櫓がなされな
い。In addition, if the amount of component (b) or component (C) exceeds 40% by weight, the detergency and foaming power will decrease, and if component (b)
If the weight of component (C) is less than 15% by weight, the viscosity stability and shape retention at high temperatures will not be improved.
添付図面は、上記の(a)〜(C)成分を各頂点とする
三角図表をもって、本発明のN−アシル酸性アミノ酸系
混合物の組成を表わしたものであって、この混合物は、
A点[: (a)−65,0、(b)= 5.0 、
(c)−30,0] 、 B点((a)−65,0,(
b) −20,0,(c) −15,0] 、 C点〔
(a)−45,0,(b) −40,0,(c)−15
,0] 、 D点(: (a)−30,0,(b)=
40.0. (c) −30,0] 、 K点[(a)
−30,0,(b) −30,0,(c)−40,0、
] 、 F点C(a)−55,O,(b) −5,0,
(c)−40,0]の6点を結んだ範囲内にあることが
必要である。The attached drawing shows the composition of the N-acyl acidic amino acid mixture of the present invention using a triangular diagram with the above-mentioned components (a) to (C) as the vertices.
Point A [: (a) -65,0, (b) = 5.0,
(c)-30,0], point B ((a)-65,0,(
b) −20,0, (c) −15,0], point C [
(a) -45,0, (b) -40,0, (c) -15
, 0], D point (: (a) - 30, 0, (b) =
40.0. (c) −30,0], K point [(a)
-30,0, (b) -30,0, (c) -40,0,
], F point C(a)-55,O,(b)-5,0,
(c) -40,0].
さらに、本発明組成物においては、このような組成をも
つN−アシル酸性アミノ酸系混合物を組成物全量に基づ
き15〜40重量係の範囲で含有することが必要であシ
、この景が15重量係未満では、洗浄剤としての能力が
低下するし、これが40重重量上りも多くなるとクリー
ム状態の維持が困難になる上に高温下での粘度安定性が
不十分になる。Furthermore, in the composition of the present invention, it is necessary to contain the N-acyl acidic amino acid mixture having such a composition in a range of 15 to 40% by weight based on the total amount of the composition. If it is less than 40% by weight, its ability as a detergent will be reduced, and if it exceeds 40% by weight, it will be difficult to maintain a creamy state and the viscosity stability at high temperatures will be insufficient.
本発明組成物には、前記N−アシル酸性アミノ酸系混合
物のほかに、必要に応じて通常の皮膚洗浄剤に慣用され
ている添加剤を適宜配合させることができる。このよう
なものとしては、例えば高級脂肪酸、高級アルコール、
高級脂肪酸グリセリドのような加脂防剤、グリセリン、
プロピレングリコール、ソルビトール、ポリエチレンク
リコールのような保湿剤、その他殺菌剤、消炎剤、酸化
防止剤、キレート剤、香料、着色剤などを挙げることが
できる。In addition to the N-acyl acidic amino acid mixture, the composition of the present invention may contain additives commonly used in ordinary skin cleansers, if necessary. Examples of such substances include higher fatty acids, higher alcohols,
Antilipidating agents such as higher fatty acid glycerides, glycerin,
Examples include humectants such as propylene glycol, sorbitol, and polyethylene glycol, as well as other disinfectants, anti-inflammatory agents, antioxidants, chelating agents, fragrances, and coloring agents.
一般にN−アシル酸性アミノ酸系混合物を含むクリーム
状皮膚洗浄剤組成物を製造するには、必要な成分の所定
量を水性媒質中に加え、加熱溶解後冷却する方法、過剰
量の遊離N−アシル酸性アミノ酸を水性媒質中に溶解し
、これに所定量の水溶性の金属化合物又は有機アミンを
加え部分的に中和させて、N−アシル酸性アミノ酸の塩
を形成させたのち、必要な添加剤を加え混合する方法が
用いられる。そして、本発明組成物もこれらの方法を用
いて調製することができるが、特に以下の方法を用いる
のが有利である。Generally, in order to produce a creamy skin cleansing composition containing a mixture of N-acyl acidic amino acids, a predetermined amount of the necessary ingredients is added to an aqueous medium, dissolved by heating, and then cooled. An acidic amino acid is dissolved in an aqueous medium, and a predetermined amount of a water-soluble metal compound or an organic amine is added thereto to partially neutralize it to form a salt of an N-acyl acidic amino acid, and then necessary additives are added. A method of adding and mixing is used. Although the composition of the present invention can also be prepared using these methods, it is particularly advantageous to use the following method.
すなわち、水性媒質中にクリーム形成に必要な成分例え
ば乳化剤、湿潤剤、分散安定剤などを溶解し、次いでこ
の中にN−アシル酸性アミノ酸のアルカリ金属塩及び有
機アミン塩の中から選ばれた少なくとも1種の化合物を
加えたのち、さらに水溶性多価金属化合物及び有機酸を
加える。この際のN−アシル酸性アミノ酸のアルカリ金
属塩及び有機アミン塩の量は、本発明組成物の(a)
、 (b)及び(C)成分を供給するのに十分な量であ
シ、水溶性多価金属化合物は、N−アシル酸性アミノ酸
のアルカリ金属塩及び有機アミン塩の一部とイオン交換
して、必要な(b)成分を供給するのに十分なlであシ
、有機酸はN−アシル酸性アミノ酸のアルカリ金属塩及
び有機アミン塩の一部を加水分解して。That is, ingredients necessary for cream formation, such as emulsifiers, wetting agents, dispersion stabilizers, etc., are dissolved in an aqueous medium, and then at least one selected from alkali metal salts and organic amine salts of N-acyl acidic amino acids is dissolved in the aqueous medium. After adding one type of compound, a water-soluble polyvalent metal compound and an organic acid are further added. In this case, the amount of the alkali metal salt and organic amine salt of the N-acyl acidic amino acid is determined as (a) of the composition of the present invention.
, the water-soluble polyvalent metal compound is ion-exchanged with a portion of the alkali metal salt and organic amine salt of the N-acyl acidic amino acid in an amount sufficient to supply components (b) and (C). , sufficient l to supply the necessary component (b), and the organic acid hydrolyzes a portion of the alkali metal salt and organic amine salt of the N-acyl acidic amino acid.
必要な(C)成分を供給するのに十分な量である。The amount is sufficient to supply the necessary component (C).
この際使用される水性媒質としては、精製した水を単独
で用いてもよいし、水と水混和性溶媒例エバエチルアル
コール、フロビルアルコール、エチレングリコールのよ
うなアルコール類との混合物を用いてもよい。As the aqueous medium used at this time, purified water may be used alone, or a mixture of water and a water-miscible solvent such as alcohol such as ethyl alcohol, furoyl alcohol, or ethylene glycol may be used. Good too.
原料として用いられるN−アシル酸性アミノ酸のアルカ
リ金属塩及び有機アミン塩は、前記(a)成分の例とし
て挙げた化合物の中から任意に選ばれる。また、水溶性
多価金属化合物としては、ベリリウム、マグネシウム、
カルシウム、バリウム。The alkali metal salt and organic amine salt of N-acyl acidic amino acid used as raw materials are arbitrarily selected from the compounds listed as examples of component (a). In addition, water-soluble polyvalent metal compounds include beryllium, magnesium,
Calcium, barium.
亜鉛、アルミニウムのハロゲン化物、硫酸塩、炭酸塩、
硝酸塩、水酸化物、例えば塩化カルシウム、硫酸マグネ
シウム、硫酸アルミニウム、塩化亜鉛、塩化マグネシウ
ムなどが用いられる。有機酸としては1例えば酢酸、乳
酸、グルコン酸、ピロリドンカルボン酸、グリシンのよ
うな一塩基酸、リンゴ酸、酒石酸、コハク酸、アジピン
酸、マレイン酸、フマル酸、グルタミン酸、アスパラジ
ン酸のような二塩基酸、クエン酸、イソクエン酸、ニト
リロトリ酢酸のような三塩基酸などが用いられる。Zinc, aluminum halides, sulfates, carbonates,
Nitrates, hydroxides such as calcium chloride, magnesium sulfate, aluminum sulfate, zinc chloride, magnesium chloride, etc. are used. Examples of organic acids include monobasic acids such as acetic acid, lactic acid, gluconic acid, pyrrolidonecarboxylic acid, and glycine, malic acid, tartaric acid, succinic acid, adipic acid, maleic acid, fumaric acid, glutamic acid, and asparadic acid. Dibasic acids, citric acid, isocitric acid, tribasic acids such as nitrilotriacetic acid, etc. are used.
これらの水溶性多価金属化合物や有機酸は、いずれも単
独で用いてもよいし、また2種以上の混合物として用い
てもよい。These water-soluble polyvalent metal compounds and organic acids may be used alone or as a mixture of two or more.
本発明組成物は、これらの必要な成分に所望成分を加え
、50〜100℃で加熱溶解させた混合物を、かきまぜ
ながら反応させ、反応終了後、室温まで冷却することに
よって得られる。この際の反応時間は、通常5〜60分
間程度である。The composition of the present invention can be obtained by adding desired components to these necessary components, heating and dissolving the mixture at 50 to 100° C., reacting the mixture with stirring, and cooling the mixture to room temperature after the reaction is completed. The reaction time at this time is usually about 5 to 60 minutes.
このようにして、均質に分散したクリーム状皮膚洗浄剤
組成物が得られる。In this way, a homogeneously dispersed creamy skin cleansing composition is obtained.
発明の効果
本発明組成物は、皮膚に対する刺激が少なく、すすぎ時
にぬめシ感が迅速に除かれ、かつ高温での粘度安定性、
保形性が良好なりリーム状皮膚洗浄剤なので、皮膚敏感
症の人や皮膚病患者用として好適に使用することができ
る上に、夏期、あるいは熱帯地域においてもその使用感
や外観に変化がなく、商品価値の低下をもたらさないと
いう利点がある。Effects of the Invention The composition of the present invention is less irritating to the skin, quickly removes the slimy feeling upon rinsing, and has good viscosity stability at high temperatures.
Since it is a cream-like skin cleansing agent with good shape retention, it can be suitably used for people with skin sensitivities and patients with skin diseases, and there is no change in its feel or appearance even in summer or in tropical regions. , it has the advantage of not causing a decrease in product value.
実施例
次に実施例によシ本発明をさらに詳細に説明する。なお
各側における性能及び物性の評価は以下の方法で行った
。EXAMPLES Next, the present invention will be explained in more detail by way of examples. The performance and physical properties of each side were evaluated using the following method.
(1)すすぎ性
女性20名をパネラ−として用い、洗顔による官能試験
を行い、次の基準で評価した。(1) Rinseability A sensory test was conducted using 20 women as panelists by washing their faces, and evaluations were made based on the following criteria.
◎・・・簡単なすすぎによシ容易にぬめシがなくなる。◎・・・Slimy stains are easily removed by simple rinsing.
○・・・ややすすぎ回数を増やすことによシ、ぬめシが
なくなる。○... Slightly increasing the number of rinses will eliminate stains and slime.
Δ・・・かなりすすがないとぬめりがなくならない。Δ...The slime doesn't go away unless you rinse it out a lot.
×・・・いつ1でもぬめシが残シネ快である。×...Numeshi is always nice to leave.
(2)高温保形性 洗浄剤をポリエチレン製のチューブに充てんし。(2) High temperature shape retention Fill a polyethylene tube with cleaning agent.
45℃の恒温槽中に10日間放置した後、りIJ −ム
をチューブから押し出し、出されたクリームの形状につ
いて以下の基準で評価した。After being left in a constant temperature bath at 45° C. for 10 days, the cream was extruded from the tube and the shape of the cream was evaluated according to the following criteria.
5・・・押し出したクリームの上部はチュープロ元形状
の円形がそのまま保たれているが、板との接触面が平ら
になる。5... The top of the extruded cream retains its original circular shape, but the surface in contact with the plate becomes flat.
4・・・押し出したクリームの上部はほぼ口元形状の円
形がそのまま保たれているが、板との接触面がかなシ拡
大【7ている。4...The upper part of the extruded cream retains its circular shape, roughly in the shape of the mouth, but the contact surface with the plate has been enlarged [7].
3・・・押し出したクリームの上部がやや扁平になシ、
板との接触面もさらに拡大している。3...The top of the extruded cream should be slightly flat,
The contact surface with the board has also been expanded.
2・・・押し出したクリームの上部がさらに扁平になシ
板との接触面が著しく拡大している。2...The upper part of the extruded cream is even flatter and the contact surface with the plate is significantly expanded.
1・・・押し出したとき、クリームがただちに板上に流
延する。1...When extruded, the cream immediately spreads onto the board.
(3)高温粘度安定性
洗浄剤を45℃の恒温槽に20日間放置し、B型粘度計
(BH型、7番ローター、10rpm、東京計器■製)
にて粘度を測定し以下の基準で評価した。(3) High-temperature viscosity stability The detergent was left in a constant temperature bath at 45°C for 20 days, and a B-type viscometer (BH type, No. 7 rotor, 10 rpm, manufactured by Tokyo Keiki ■) was used.
The viscosity was measured and evaluated based on the following criteria.
O・・・45℃で放置したとき、1日後と20日後の粘
度差が200p以下である。O: When left at 45°C, the difference in viscosity between 1 day and 20 days is 200p or less.
Δ・・・45℃で放置したとき、1日後と20日後の粘
度差が200〜400pの間である。Δ: When left at 45° C., the difference in viscosity after 1 day and after 20 days is between 200 and 400 p.
×・・・45℃で放置したとき、1日後と20日後の粘
度差が400p以上である。x: When left at 45°C, the difference in viscosity after 1 day and after 20 days is 400p or more.
実施例1〜4.比較例1〜4
第1表に示す比率の(a) 、 (1))及び(c)と
プロピレングリコール、ポリエチレングリコール(15
00)の所定量を精製水とともにビーカーに入れ混合し
加熱溶解することにより70℃の混合物中を調製する。Examples 1-4. Comparative Examples 1 to 4 Propylene glycol, polyethylene glycol (15
A predetermined amount of 00) is mixed with purified water in a beaker, and the mixture is heated and dissolved to prepare a mixture at 70°C.
別にPOE (4010,)硬化ヒマシ油モノステアレ
ート、グリセリンモノステアレート及びパルミチン酸の
所定量をビーカーに入れ加熱溶解して混合物(n)を調
製する。Separately, a mixture (n) is prepared by placing predetermined amounts of POE (4010,) hydrogenated castor oil monostearate, glycerin monostearate, and palmitic acid in a beaker and dissolving them under heating.
次いで、混合物(1)に混合物(II)を添加し、70
℃において10分間かきまぜて均質化したのち、かきま
ぜながら室温まで冷却し、クリーム状皮膚洗浄剤とする
。Next, mixture (II) was added to mixture (1), and 70
After stirring for 10 minutes at ℃ to homogenize, the mixture is cooled to room temperature while stirring to obtain a creamy skin cleansing agent.
このようにして、(a) N−ミリストイルグルタミン
酸ナトリクム、(b)N−ミリストイルグルタミン酸マ
グネシウム、(c) N−ミリストイルグルタミン酸の
3成分の総量が組成物全景の20重量%及びプロピレン
グリコール15重量%、ポリエチレングリコール(15
00) 10重量%、POK (40B、O,)硬化ヒ
マシ油モノステアレート3重量係、グリセリンモノステ
アレート1重量%及びパルミチン酸2重量%と全量が1
003量チになるまでの精製水を含むクリーム状皮膚洗
浄剤を得た。このものの性能を第1表に示す。In this way, the total amount of the three components (a) sodium N-myristoylglutamate, (b) magnesium N-myristoylglutamate, and (c) N-myristoylglutamic acid is 20% by weight of the entire composition, propylene glycol 15% by weight, Polyethylene glycol (15
00) 10% by weight, POK (40B, O,) 3% by weight of hydrogenated castor oil monostearate, 1% by weight of glycerin monostearate and 2% by weight of palmitic acid, and the total amount is 1% by weight.
A cream skin cleansing agent containing purified water up to 0.003% was obtained. The performance of this product is shown in Table 1.
この表から明らかなように、(、)成分30〜65重量
%、(b)成分5〜40重量1(C)成分15〜40重
量係の範囲内にあるものは性能、物性のすべてにおいて
良好であったが、その範囲外のものは、性能、物性のい
ずれかが不十分であった。As is clear from this table, components within the range of 30 to 65% by weight of components (,), 5 to 40% by weight of component (b), and 15 to 40% by weight of component (C) have good performance and physical properties. However, those outside this range had insufficient performance or physical properties.
実施例5〜11
第2表に示す成分を用いクリーム状皮膚洗浄剤を調製し
た。すなわち、N−ミリストイルグルタミン酸、ンルビ
トール及びポリエチレングリコール400を精製水と混
合し加熱溶解したのち、水溶性二価金属塩又はその代替
物及び有機酸又はその塩を添加し攪拌溶解した後混合物
CI)を調製する。Examples 5 to 11 Creamy skin cleansers were prepared using the ingredients shown in Table 2. That is, after mixing N-myristoyl glutamic acid, nrubitol, and polyethylene glycol 400 with purified water and heating and dissolving it, a water-soluble divalent metal salt or its substitute and an organic acid or its salt were added and dissolved with stirring, and then the mixture CI) was prepared. Prepare.
別にミリスチン酸、グリセリンモノオレエート及びPO
E硬化硬化ヒマシリトリイソステアレート混合加熱溶解
して混合物[11〕を調製する。次に混合物CDに混合
物[11を添加し攪拌して均質化した後攪拌しながら室
温まで冷却してクリーム状皮膚洗浄剤とした。このよう
にして得た試料の性能及び物性を第2表に示す。Separately myristic acid, glycerin monooleate and PO
E-cure Cured castor triisostearate is mixed and heated to dissolve to prepare a mixture [11]. Next, mixture [11] was added to mixture CD, stirred to homogenize, and then cooled to room temperature while stirring to obtain a cream-like skin cleansing agent. Table 2 shows the performance and physical properties of the sample thus obtained.
この表からも分るように必、須の3成分が所定の比率内
で形成される場合(ム1,2)は性能及び物性とも良好
であるが、二価金属塩が形成されない場合(43,4,
7)又は酸が形成されない場合(45,6,7)はいず
れも性能又は物性が劣っていた。さらに、これらの試料
はいずれも調製時の変色、変臭等の品質の劣化は認めら
れなかった。As can be seen from this table, performance and physical properties are good when the three essential components are formed within a predetermined ratio (Mu 1 and 2), but when divalent metal salts are not formed (Mu 43), the performance and physical properties are good. ,4,
7) or when no acid was formed (45, 6, 7), the performance or physical properties were poor. Furthermore, no deterioration in quality such as discoloration or odor during preparation was observed in any of these samples.
実施例12 次に示す成分を用いクリーム状皮膚洗浄剤を調製した。Example 12 A cream skin cleansing agent was prepared using the ingredients shown below.
すなわち、N−ラウロイルグルタミン酸ナトリウム、N
−ミリストイルグルタミン酸ナトリウム、プロピレング
リコール及びンルビトールを精製水に混合し加熱溶解し
た中ヘコノ・り酸及び硫酸マグネシウムを加え攪拌溶解
し混合物〔l〕を調製する。別にラウリン酸、ポリオキ
シエチレン(40)硬化ヒマシ油モノラウレート、ヤシ
油脂肪酸ジェタノールアミド及びグリセリルモノステア
レートを混合加熱溶解して混合物[I[]を調製する。Namely, sodium N-lauroylglutamate, N
- Mix sodium myristoyl glutamate, propylene glycol, and nrubitol in purified water, heat-dissolve it, add hecono-phosphoric acid and magnesium sulfate, and dissolve with stirring to prepare a mixture [1]. Separately, a mixture [I[] is prepared by mixing and heating and dissolving lauric acid, polyoxyethylene (40) hydrogenated castor oil monolaurate, coconut oil fatty acid jetanolamide, and glyceryl monostearate.
次いで混合物〔■〕に混合物[11を添加し70℃にお
いて10分間かきまぜ均質化した後攪拌しながら室温ま
で冷却してクリーム状皮膚洗浄剤とした。Next, mixture [11] was added to mixture [■], stirred at 70° C. for 10 minutes to homogenize, and then cooled to room temperature while stirring to obtain a creamy skin cleansing agent.
なお、この組成物における必須成分(a)、 (b)、
(C)の比率は(a):(b):(c)= 53 :
24 : 23である。In addition, essential components (a), (b),
The ratio of (C) is (a):(b):(c)=53:
24:23.
得られたクリーム状皮膚洗浄剤はすすぎ性、高温保形性
及び粘度安定性が優れているだけでなく、調製が非常に
簡単で、調製時の着色、変臭等の問題もなく良好であっ
た。The obtained creamy skin cleanser not only has excellent rinsability, high-temperature shape retention, and viscosity stability, but is also very easy to prepare and has no problems such as coloring or odor during preparation. Ta.
ラム 20.O
N−ミリストイルグルタミン酸ナト
リウム 5.0
ラウリン酸 3.0ヤシ油脂肪酸
ジエタノールアミド 1.0グリセリルモノ
ステアレート 0.5プロピレングリコ
ール 20.0ソルビトール
8.0コハク酸
1.0硫酸マグネシウム
i、。Ram 20. O
Sodium N-myristoylglutamate 5.0
Lauric acid 3.0 Coco fatty acid diethanolamide 1.0 Glyceryl monostearate 0.5 Propylene glycol 20.0 Sorbitol
8.0 Succinic acid
1.0 Magnesium Sulfate
i.
香 料 0
.3精製水 38.2Fragrance 0
.. 3 Purified water 38.2
図は1本発明組成物に用いるN−アシル酸性アミノ酸系
混合物の組成範囲を示す三角図表である。
特許出願人 ライオン株式会社The figure is a triangular diagram showing the composition range of the N-acyl acidic amino acid mixture used in the composition of the present invention. Patent applicant Lion Corporation
Claims (1)
び有機アミン塩の中から選ばれた少なくとも1種の成分
30〜65重量%、(b)N−アシル酸性アミノ酸の多
価金属塩の中から選ばれた少なくとも1種の成分5〜4
0重量%及び(c)N−アシル酸性アミノ酸の中から選
ばれた少なくとも1種の成分15〜40重量%から成る
N−アシル酸性アミノ酸系混合物を、組成物全量に基づ
き15〜40重量%含有したことを特徴とするクリーム
状皮膚洗浄剤組成物。 2 クリーム形成に必要な成分を含む水性媒質中に、所
要量のN−アシル酸性アミノ酸のアルカリ金属塩及び有
機アミン塩の中から選ばれた少なくとも1種の化合物を
溶解し、これに所要量の水溶性多価金属化合物及び有機
酸を加え、かきまぜながら加熱反応させることを特徴と
する、(a)N−アシル酸性アミノ酸のアルカリ金属塩
及び有機アミン塩の中から選ばれた少なくとも1種の成
分30〜65重量%、(b)N−アシル酸性アミノ酸の
多価金属塩の中から選ばれた少なくとも1種の成分5〜
40重量%及び(c)N−アシル酸性アミノ酸の中から
選ばれた少なくとも1種の成分15〜40重量%から成
るN−アシル酸性アミノ酸系混合物を、組成物全量に基
づき15〜40重量%含有したクリーム状皮膚洗浄剤組
成物の製造方法。[Scope of Claims] 1 (a) 30 to 65% by weight of at least one component selected from alkali metal salts and organic amine salts of N-acyl acidic amino acids; (b) polyester of N-acyl acidic amino acids; At least one component selected from valent metal salts 5 to 4
Contains 15 to 40% by weight of an N-acyl acidic amino acid mixture consisting of 0% by weight and (c) 15 to 40% by weight of at least one component selected from N-acyl acidic amino acids, based on the total amount of the composition. A creamy skin cleansing composition characterized by: 2. Dissolve a required amount of at least one compound selected from alkali metal salts and organic amine salts of N-acyl acidic amino acids in an aqueous medium containing the ingredients necessary for cream formation, and add the required amount of at least one compound selected from the alkali metal salts and organic amine salts of N-acyl acidic amino acids. (a) At least one component selected from alkali metal salts and organic amine salts of N-acyl acidic amino acids, characterized in that a water-soluble polyvalent metal compound and an organic acid are added and reacted with heating while stirring. 30-65% by weight, (b) at least one component selected from polyvalent metal salts of N-acyl acidic amino acids5-
Contains 15 to 40% by weight of an N-acyl acidic amino acid mixture consisting of 40% by weight and (c) 15 to 40% by weight of at least one component selected from N-acyl acidic amino acids, based on the total amount of the composition. A method for producing a creamy skin cleansing composition.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP30462987A JP2609644B2 (en) | 1987-12-03 | 1987-12-03 | Skin cleansing composition and method for producing the same |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP30462987A JP2609644B2 (en) | 1987-12-03 | 1987-12-03 | Skin cleansing composition and method for producing the same |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH01146816A true JPH01146816A (en) | 1989-06-08 |
JP2609644B2 JP2609644B2 (en) | 1997-05-14 |
Family
ID=17935333
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP30462987A Expired - Lifetime JP2609644B2 (en) | 1987-12-03 | 1987-12-03 | Skin cleansing composition and method for producing the same |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP2609644B2 (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0761203A1 (en) * | 1995-09-07 | 1997-03-12 | L'oreal | Use of cysteine acid homocysteine for enhancing the desquamation of the skin or to stimulate the renewal of the epidermis |
JP2007014264A (en) * | 2005-07-07 | 2007-01-25 | Iseki & Co Ltd | Multiple row applicator |
US8383090B2 (en) | 2003-07-17 | 2013-02-26 | Zschimmer & Schwarz Italiana S.P.A. | Cleansing composition based on oily substances |
JP2017066048A (en) * | 2015-09-28 | 2017-04-06 | 味の素株式会社 | Creamy detergent compositions and production methods thereof |
-
1987
- 1987-12-03 JP JP30462987A patent/JP2609644B2/en not_active Expired - Lifetime
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0761203A1 (en) * | 1995-09-07 | 1997-03-12 | L'oreal | Use of cysteine acid homocysteine for enhancing the desquamation of the skin or to stimulate the renewal of the epidermis |
FR2738484A1 (en) * | 1995-09-07 | 1997-03-14 | Oreal | USE OF CYSTEIC OR HOMOCYSTEIC ACID TO PROMOTE SKIN DEQUAMATION OR STIMULATE EPIDERMAL RENEWAL |
US8383090B2 (en) | 2003-07-17 | 2013-02-26 | Zschimmer & Schwarz Italiana S.P.A. | Cleansing composition based on oily substances |
JP2007014264A (en) * | 2005-07-07 | 2007-01-25 | Iseki & Co Ltd | Multiple row applicator |
JP2017066048A (en) * | 2015-09-28 | 2017-04-06 | 味の素株式会社 | Creamy detergent compositions and production methods thereof |
Also Published As
Publication number | Publication date |
---|---|
JP2609644B2 (en) | 1997-05-14 |
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