JPS643529B2 - - Google Patents
Info
- Publication number
- JPS643529B2 JPS643529B2 JP55114376A JP11437680A JPS643529B2 JP S643529 B2 JPS643529 B2 JP S643529B2 JP 55114376 A JP55114376 A JP 55114376A JP 11437680 A JP11437680 A JP 11437680A JP S643529 B2 JPS643529 B2 JP S643529B2
- Authority
- JP
- Japan
- Prior art keywords
- oil
- weight
- higher fatty
- phase component
- water
- 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.)
- Expired
Links
- 239000000203 mixture Substances 0.000 claims description 34
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 25
- 239000000194 fatty acid Substances 0.000 claims description 25
- 229930195729 fatty acid Natural products 0.000 claims description 25
- 150000004665 fatty acids Chemical class 0.000 claims description 25
- 239000007764 o/w emulsion Substances 0.000 claims description 19
- 239000002734 clay mineral Substances 0.000 claims description 15
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 15
- 238000004519 manufacturing process Methods 0.000 claims description 13
- 238000003756 stirring Methods 0.000 claims description 13
- 239000000126 substance Substances 0.000 claims description 12
- GUJOJGAPFQRJSV-UHFFFAOYSA-N dialuminum;dioxosilane;oxygen(2-);hydrate Chemical group O.[O-2].[O-2].[O-2].[Al+3].[Al+3].O=[Si]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O GUJOJGAPFQRJSV-UHFFFAOYSA-N 0.000 claims description 6
- RJDOZRNNYVAULJ-UHFFFAOYSA-L [O--].[O--].[O--].[O--].[O--].[O--].[O--].[O--].[O--].[O--].[F-].[F-].[Mg++].[Mg++].[Mg++].[Al+3].[Si+4].[Si+4].[Si+4].[K+] Chemical compound [O--].[O--].[O--].[O--].[O--].[O--].[O--].[O--].[O--].[O--].[F-].[F-].[Mg++].[Mg++].[Mg++].[Al+3].[Si+4].[Si+4].[Si+4].[K+] RJDOZRNNYVAULJ-UHFFFAOYSA-L 0.000 claims description 3
- 238000001816 cooling Methods 0.000 claims description 3
- 238000002156 mixing Methods 0.000 claims description 3
- 229910000278 bentonite Inorganic materials 0.000 claims description 2
- 239000000440 bentonite Substances 0.000 claims description 2
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 claims description 2
- 239000003921 oil Substances 0.000 description 20
- 235000019198 oils Nutrition 0.000 description 20
- 239000012071 phase Substances 0.000 description 20
- 239000000839 emulsion Substances 0.000 description 18
- AZJYLVAUMGUUBL-UHFFFAOYSA-A u1qj22mc8e Chemical compound [F-].[F-].[F-].[F-].[F-].[F-].[F-].[F-].[F-].[F-].[F-].[F-].[F-].[F-].[F-].[F-].[F-].[F-].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].O=[Si]=O.O=[Si]=O.O=[Si]=O.O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3.O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3.O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3.O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3.O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3.O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3 AZJYLVAUMGUUBL-UHFFFAOYSA-A 0.000 description 13
- 239000002537 cosmetic Substances 0.000 description 11
- 239000004094 surface-active agent Substances 0.000 description 10
- 239000000499 gel Substances 0.000 description 9
- 239000008346 aqueous phase Substances 0.000 description 8
- 239000000047 product Substances 0.000 description 8
- 239000008117 stearic acid Substances 0.000 description 8
- 235000021355 Stearic acid Nutrition 0.000 description 7
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 7
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 7
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 6
- 239000006071 cream Substances 0.000 description 6
- 238000011156 evaluation Methods 0.000 description 5
- -1 For example Substances 0.000 description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- 229940057995 liquid paraffin Drugs 0.000 description 4
- 239000012188 paraffin wax Substances 0.000 description 4
- 238000000926 separation method Methods 0.000 description 4
- 239000007787 solid Substances 0.000 description 4
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 239000002585 base Substances 0.000 description 3
- 235000013871 bee wax Nutrition 0.000 description 3
- 239000012166 beeswax Substances 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 238000004945 emulsification Methods 0.000 description 3
- 235000019441 ethanol Nutrition 0.000 description 3
- XOJVVFBFDXDTEG-UHFFFAOYSA-N pristane Chemical compound CC(C)CCCC(C)CCCC(C)CCCC(C)C XOJVVFBFDXDTEG-UHFFFAOYSA-N 0.000 description 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- 206010040880 Skin irritation Diseases 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 235000012216 bentonite Nutrition 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 239000008278 cosmetic cream Substances 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
- 230000001804 emulsifying effect Effects 0.000 description 2
- 239000003205 fragrance Substances 0.000 description 2
- 235000021588 free fatty acids Nutrition 0.000 description 2
- 238000001879 gelation Methods 0.000 description 2
- 239000003349 gelling agent Substances 0.000 description 2
- IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 2
- 229940094522 laponite Drugs 0.000 description 2
- XCOBTUNSZUJCDH-UHFFFAOYSA-B lithium magnesium sodium silicate Chemical compound [Li+].[Li+].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[Na+].[Na+].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3.O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3.O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3.O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3.O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3.O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3 XCOBTUNSZUJCDH-UHFFFAOYSA-B 0.000 description 2
- 230000000704 physical effect Effects 0.000 description 2
- 239000000049 pigment Substances 0.000 description 2
- 239000003755 preservative agent Substances 0.000 description 2
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 2
- 230000036556 skin irritation Effects 0.000 description 2
- 231100000475 skin irritation Toxicity 0.000 description 2
- 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 2
- 239000001993 wax Substances 0.000 description 2
- 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
- DGSZGZSCHSQXFV-UHFFFAOYSA-N 2,3-bis(2-ethylhexanoyloxy)propyl 2-ethylhexanoate Chemical compound CCCCC(CC)C(=O)OCC(OC(=O)C(CC)CCCC)COC(=O)C(CC)CCCC DGSZGZSCHSQXFV-UHFFFAOYSA-N 0.000 description 1
- KUIYXYIWGVFQPD-UHFFFAOYSA-N 2-octyldodecanoic acid Chemical compound CCCCCCCCCCC(C(O)=O)CCCCCCCC KUIYXYIWGVFQPD-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
- CYDQOEWLBCCFJZ-UHFFFAOYSA-N 4-(4-fluorophenyl)oxane-4-carboxylic acid Chemical compound C=1C=C(F)C=CC=1C1(C(=O)O)CCOCC1 CYDQOEWLBCCFJZ-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
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
- 235000019489 Almond oil Nutrition 0.000 description 1
- 235000021357 Behenic acid Nutrition 0.000 description 1
- 229920002101 Chitin Polymers 0.000 description 1
- 239000004166 Lanolin Substances 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
- 235000021314 Palmitic acid Nutrition 0.000 description 1
- 239000004264 Petrolatum Substances 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- 229920002385 Sodium hyaluronate Polymers 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
- 239000003513 alkali Substances 0.000 description 1
- 150000005215 alkyl ethers Chemical class 0.000 description 1
- 239000008168 almond oil Substances 0.000 description 1
- 150000001413 amino acids Chemical class 0.000 description 1
- 229940116226 behenic acid Drugs 0.000 description 1
- VNSBYDPZHCQWNB-UHFFFAOYSA-N calcium;aluminum;dioxido(oxo)silane;sodium;hydrate Chemical compound O.[Na].[Al].[Ca+2].[O-][Si]([O-])=O VNSBYDPZHCQWNB-UHFFFAOYSA-N 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 229960000541 cetyl alcohol Drugs 0.000 description 1
- 239000002738 chelating agent Substances 0.000 description 1
- KXKPYJOVDUMHGS-OSRGNVMNSA-N chondroitin sulfate Chemical compound CC(=O)N[C@H]1[C@H](O)O[C@H](OS(O)(=O)=O)[C@H](O)[C@@H]1O[C@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](C(O)=O)O1 KXKPYJOVDUMHGS-OSRGNVMNSA-N 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 229940105990 diglycerin Drugs 0.000 description 1
- GPLRAVKSCUXZTP-UHFFFAOYSA-N diglycerol Chemical compound OCC(O)COCC(O)CO GPLRAVKSCUXZTP-UHFFFAOYSA-N 0.000 description 1
- 239000003974 emollient agent Substances 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 229940093476 ethylene glycol Drugs 0.000 description 1
- 239000003925 fat Substances 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 229960005150 glycerol Drugs 0.000 description 1
- 229910000271 hectorite Inorganic materials 0.000 description 1
- KWLMIXQRALPRBC-UHFFFAOYSA-L hectorite Chemical compound [Li+].[OH-].[OH-].[Na+].[Mg+2].O1[Si]2([O-])O[Si]1([O-])O[Si]([O-])(O1)O[Si]1([O-])O2 KWLMIXQRALPRBC-UHFFFAOYSA-L 0.000 description 1
- BXWNKGSJHAJOGX-UHFFFAOYSA-N hexadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 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
- 235000019388 lanolin Nutrition 0.000 description 1
- 229940039717 lanolin 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
- 238000000034 method Methods 0.000 description 1
- 229910052901 montmorillonite Inorganic materials 0.000 description 1
- 229940105132 myristate Drugs 0.000 description 1
- WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 1
- JXTPJDDICSTXJX-UHFFFAOYSA-N n-Triacontane Natural products CCCCCCCCCCCCCCCCCCCCCCCCCCCCCC JXTPJDDICSTXJX-UHFFFAOYSA-N 0.000 description 1
- 239000005445 natural material Substances 0.000 description 1
- 230000003472 neutralizing effect Effects 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- 229910000273 nontronite Inorganic materials 0.000 description 1
- 235000014593 oils and fats Nutrition 0.000 description 1
- 239000003883 ointment base Substances 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 229940055577 oleyl alcohol Drugs 0.000 description 1
- XMLQWXUVTXCDDL-UHFFFAOYSA-N oleyl alcohol Natural products CCCCCCC=CCCCCCCCCCCO XMLQWXUVTXCDDL-UHFFFAOYSA-N 0.000 description 1
- 239000004006 olive oil Substances 0.000 description 1
- 235000008390 olive oil Nutrition 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 229940066842 petrolatum Drugs 0.000 description 1
- 235000019271 petrolatum Nutrition 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 229960004063 propylene glycol Drugs 0.000 description 1
- 235000013772 propylene glycol Nutrition 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 229920002545 silicone oil Polymers 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 229940010747 sodium hyaluronate Drugs 0.000 description 1
- 239000001540 sodium lactate Substances 0.000 description 1
- 229940005581 sodium lactate Drugs 0.000 description 1
- 235000011088 sodium lactate Nutrition 0.000 description 1
- 229940045920 sodium pyrrolidone carboxylate Drugs 0.000 description 1
- YWIVKILSMZOHHF-QJZPQSOGSA-N sodium;(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- Chemical compound [Na+].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 YWIVKILSMZOHHF-QJZPQSOGSA-N 0.000 description 1
- HYRLWUFWDYFEES-UHFFFAOYSA-M sodium;2-oxopyrrolidine-1-carboxylate Chemical compound [Na+].[O-]C(=O)N1CCCC1=O HYRLWUFWDYFEES-UHFFFAOYSA-M 0.000 description 1
- 229940032094 squalane Drugs 0.000 description 1
- TUNFSRHWOTWDNC-UHFFFAOYSA-N tetradecanoic acid Chemical compound CCCCCCCCCCCCCC(O)=O TUNFSRHWOTWDNC-UHFFFAOYSA-N 0.000 description 1
- TUNFSRHWOTWDNC-HKGQFRNVSA-N tetradecanoic acid Chemical compound CCCCCCCCCCCCC[14C](O)=O TUNFSRHWOTWDNC-HKGQFRNVSA-N 0.000 description 1
- 239000002562 thickening agent 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
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
- A61K8/36—Carboxylic acids; Salts or anhydrides thereof
- A61K8/361—Carboxylic acids having more than seven carbon atoms in an unbroken chain; Salts or anhydrides 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
- A61K8/02—Cosmetics or similar toiletry preparations characterised by special physical form
- A61K8/04—Dispersions; Emulsions
- A61K8/06—Emulsions
-
- 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
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Birds (AREA)
- Epidemiology (AREA)
- Dispersion Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Emergency Medicine (AREA)
- Dermatology (AREA)
- Cosmetics (AREA)
- Emulsifying, Dispersing, Foam-Producing Or Wetting Agents (AREA)
- Colloid Chemistry (AREA)
Description
本発明は親水性界面活性剤を用いることなく製
造し得る親規な水中油型乳化組成物、特に化粧料
用水中油型乳化組成物の製造法に関するものであ
る。
従来、化粧クリームの如き化粧料用水中油型乳
化組成物は、油分と水相成分とを主要成分とし、
これにその他の粉体類、色素、防腐剤、香料等を
添加することにより提供されている。この種化粧
クリームにおいては、通常、親水性界面活性剤、
例えば脂肪酸石けんや、ポリオキシエチレンアル
キルエーテル等の非イオン界面活性剤などが乳化
剤として用いられているが、例えば次のような欠
点を有し、必ずしも製品として望ましいものが提
供されているとは云い難い。
すなわち、
1 一般に、皮膚刺激が高い。
2 製造条件(温度、撹拌力、冷却速度等)が最
終製品の品質を左右し、常に均一な品質の製品
は得にくい。特に、クリームの硬度などの物理
的特性が、温度変化に強く依存する。
3 経時的に状態変化(分離、離漿等)を起し易
い。
4 ベタツキのある使用感となるため、官能的に
好ましくない場合がある。
等の点が挙げられる。このような親水性界面活性
剤による問題点を解消するため、使用量をできる
だけ少なくしたり、親水性界面活性剤を用いない
方法など種々検討されているが、未だ満足すべき
結果を得るには到つていない。
本発明者は、高級脂肪酸または高級脂肪酸含有
物質を含む油相成分と特定のゲル化能を有する粘
土鉱物とを少なくとも含有する基剤成分を、一定
の条件下において、混合強力撹拌して得られるコ
ンプレツクス(複合体)が後述するように油分を
均一に分散させる乳化機能を有し、その機能を応
用することにより、上記親水性界面活性剤を配合
した場合に生ずる諸々の欠点を解消することを見
出した。
すなわち、本発明は高級脂肪酸および/または
高級脂肪酸含有物質を含む油相成分5〜60重量
%、水相成分40〜90重量%、モンモリロナイト族
粘土鉱物、ベントナイト及び合成雲母から選ばれ
る一種以上のゲル化能を有する粘土鉱物0.5〜5
重量%からなるPH4.0〜10.5に調整された基剤成
分において、該基剤成分を混合し、次いで油相成
分が溶解している温度範囲下で強力に撹拌し、冷
却する水中油型乳化組成物の製造法に関するもの
である。
以下、本発明を詳細に説明する。
本発明に適用される油相成分としては、通常の
ものでよく、油脂類、ロウ類、炭化水素、エステ
ル類、高級アルコール類等各種あるが、具体的に
は流動パラフイン、スクワラン、プリスタン、9
−メチルノナデカン、オレイルアルコール、オリ
ーブ油、イソプロピルミリステート、ミリスチン
酸オクチルデシル、ワセリン、固型パラフイン、
シリコーン油、ラノリン、アーモンド油、2−エ
チルヘキサン酸トリグリセリド、テトラメチルペ
ンタデカン、セタノール等が挙げられる。
油相成分に含まれる高級脂肪酸としては、ラウ
リン酸、ミリスチン酸、パルミチン酸、ステアリ
ン酸、ベヘニン酸、メリシン酸、オレイン酸、12
−オキシ−ステアリン酸、2−オクチルードデカ
ン酸等の炭素数12〜30の直鎖、分岐、飽和、不飽
和およびオキシ脂肪酸である。また、高級脂肪酸
を直接用いる代わりに、高級脂肪酸を含有する物
質を用いてもよい。斯かる物質としては上記高級
脂肪酸が通常1重量%以上含有されている物質で
あればよく、例えば蜜ロウの如き遊離の脂肪酸が
含まれている天然物質が挙げられる。これらの高
級脂肪酸や高級脂肪酸含有物質は、本発明におい
て、1種または2種以上混合して用いられるもの
である。
また、この時の油相成分中に占める高級脂肪酸
の含有割合は0.01重量%以上が必要であり、好ま
しくは0.1重量%以上である。尚、上限について
は制限的ではないが、得られる乳化組成物の特性
(感触、安全性)を考慮して50重量%以下が好ま
しい。
水相成分としては、水の他、エチルアルコー
ル、プロピルアルコール、グリセリン、プロピレ
ングリコール、エチレングリコール、マルチトー
ル、ジグリセリン、乳酸ナトリウム、ピロリドン
カルボン酸ナトリウム、コンドロイチン硫酸ナト
リウム、ヒアルロン酸ナトリウム等が水と共に用
いられ、その割合としては水100部に対し1〜50
の部の範囲で置換することができる。本発明にお
いては、エチルアルコール、プロピレングリコー
ル等を多量に用いることが可能であるので、系の
防腐に効果的である。
本発明で用いられるゲル化能を有する粘土鉱物
としては、モンモリロナイト、バイデライト、ノ
ントロナイト、ヘクトライト、合成ヘクトライト
(商品名ラポナイト、Laporte Industries
Limited社製)等のモンモリロナイト族粘土鉱物
やその他ベントナイトの他、合成雲母(商品名ダ
イモライト、トピー工業社製)、ビーガム(バン
ダービルト社製)など各種のものが考えられる
が、合成品であり品質のばらつきが小さく且つ乳
化力が強い点から最も好適には前記合成ヘクトラ
イトが用いられる。本発明に係る乳化組成物にお
いて、界面活性剤に代わるコンプレツクスを生成
させるためには、前記高級脂肪酸を含む油相成分
と水相成分との混合系において、水相成分100部
に対し、ゲル化能を有する粘土鉱物1〜10部の割
合で用いることが必要である。1部未満では得ら
れるエマルジヨンがゲル化しないので、容易に排
液を起こし、安定なエマルジヨンを形成しない。
10部を超えるとゲル化が優先して起こるために均
一な乳化が起こりにくい。本発明者は、良好なエ
マルジヨンを得るのに必要な高級脂肪酸の許容量
を測定するため、次の評価試験1、2に示すよう
に、各種高級脂肪酸類、各種高級脂肪酸含有物質
の量を変化させて溶解させた油相成分49.25重量
%と水49.25重量%と合成ヘクトライト(商品名
ラポナイトXLG)1.5重量%を混合した後、80℃
にてエースホモゲナイザー(日本精機)を用いて
15000rpmの条件にて10分間撹拌して乳化させた
ところ、上記の範囲を求め得たものである。
評価試験1(ステアリン酸使用時)油相
固定パラフイン 5.0重量部
流動パラフイン 44.25−x
ステアリン酸 x 水相
水 49.25重量部粘土鉱物
合成ヘクトライト 1.5重量部
The present invention relates to a conventional oil-in-water emulsion composition that can be produced without using a hydrophilic surfactant, and particularly to a method for producing an oil-in-water emulsion composition for cosmetics. Conventionally, oil-in-water emulsion compositions for cosmetics such as cosmetic creams have oil and aqueous phase components as main components,
It is provided by adding other powders, pigments, preservatives, fragrances, etc. This type of cosmetic cream usually contains hydrophilic surfactants,
For example, fatty acid soaps and nonionic surfactants such as polyoxyethylene alkyl ethers are used as emulsifiers, but they have the following drawbacks, and it is said that they do not necessarily provide desirable products. hard. Namely: 1. Generally highly irritating to the skin. 2. Manufacturing conditions (temperature, stirring power, cooling rate, etc.) affect the quality of the final product, making it difficult to consistently obtain products of uniform quality. In particular, physical properties such as cream hardness are strongly dependent on temperature changes. 3. Conditions tend to change over time (separation, syneresis, etc.). 4 The product may have a sticky feel, which may be sensually undesirable. The following points can be mentioned. In order to solve these problems caused by hydrophilic surfactants, various methods are being considered, such as reducing the amount used as much as possible or not using hydrophilic surfactants, but it is still difficult to obtain satisfactory results. I haven't reached it yet. The present inventor has discovered that the oil phase component containing a higher fatty acid or a higher fatty acid-containing substance and a base component containing at least a clay mineral having a specific gelling ability are mixed and strongly stirred under certain conditions. As described below, complexes have an emulsifying function that uniformly disperses oil, and by applying this function, various disadvantages that occur when the above-mentioned hydrophilic surfactants are blended can be solved. I found out. That is, the present invention comprises 5 to 60% by weight of an oil phase component containing a higher fatty acid and/or a higher fatty acid-containing substance, 40 to 90% by weight of an aqueous phase component, and one or more gels selected from montmorillonite group clay minerals, bentonite, and synthetic mica. Clay minerals with chemical ability 0.5 to 5
Oil-in-water emulsification in which the base components are mixed at a pH of 4.0 to 10.5 and then stirred vigorously in a temperature range in which the oil phase components are dissolved, followed by cooling. The present invention relates to a method for producing a composition. The present invention will be explained in detail below. The oil phase components applicable to the present invention may be ordinary ones, and include various oils and fats, waxes, hydrocarbons, esters, higher alcohols, etc., but specific examples include liquid paraffin, squalane, pristane,
- Methyl nonadecane, oleyl alcohol, olive oil, isopropyl myristate, octyldecyl myristate, petrolatum, solid paraffin,
Examples include silicone oil, lanolin, almond oil, 2-ethylhexanoic acid triglyceride, tetramethylpentadecane, and cetanol. Higher fatty acids contained in the oil phase components include lauric acid, myristic acid, palmitic acid, stearic acid, behenic acid, melisic acid, oleic acid,
They are straight chain, branched, saturated, unsaturated and oxyfatty acids having 12 to 30 carbon atoms such as -oxy-stearic acid and 2-octyldodecanoic acid. Furthermore, instead of directly using higher fatty acids, a substance containing higher fatty acids may be used. Such a substance may be any substance that normally contains 1% by weight or more of the above-mentioned higher fatty acids, and includes, for example, natural substances containing free fatty acids such as beeswax. These higher fatty acids and higher fatty acid-containing substances are used singly or in combination of two or more. Further, the content of higher fatty acids in the oil phase component at this time must be 0.01% by weight or more, preferably 0.1% by weight or more. Although the upper limit is not critical, it is preferably 50% by weight or less in consideration of the characteristics (feel, safety) of the resulting emulsion composition. In addition to water, water phase components include ethyl alcohol, propyl alcohol, glycerin, propylene glycol, ethylene glycol, maltitol, diglycerin, sodium lactate, sodium pyrrolidone carboxylate, sodium chondroitin sulfate, sodium hyaluronate, etc. The ratio is 1 to 50 parts per 100 parts of water.
Can be replaced within the range of . In the present invention, since it is possible to use a large amount of ethyl alcohol, propylene glycol, etc., it is effective for preserving the system. Clay minerals with gelling ability used in the present invention include montmorillonite, beidellite, nontronite, hectorite, synthetic hectorite (trade name Laponite, Laporte Industries
In addition to montmorillonite clay minerals such as montmorillonite group clay minerals (manufactured by Limited) and other bentonites, various types of synthetic mica (trade name Daimolite, manufactured by Topy Industries, Ltd.) and Veegum (manufactured by Vanderbilt) are considered, but they are synthetic products. The synthetic hectorite is most preferably used because of its small variation in quality and strong emulsifying power. In the emulsified composition according to the present invention, in order to generate a complex in place of a surfactant, in the mixed system of the oil phase component containing the higher fatty acid and the aqueous phase component, gel is added to 100 parts of the aqueous phase component. It is necessary to use 1 to 10 parts of the clay mineral having the ability to form. If the amount is less than 1 part, the resulting emulsion will not gel, resulting in easy drainage and no stable emulsion will be formed.
If it exceeds 10 parts, gelation takes priority and uniform emulsification is difficult to occur. In order to measure the permissible amount of higher fatty acids necessary to obtain a good emulsion, the inventors varied the amounts of various higher fatty acids and various higher fatty acid-containing substances as shown in the following evaluation tests 1 and 2. After mixing 49.25% by weight of the oil phase component, 49.25% by weight of water, and 1.5% by weight of synthetic hectorite (trade name Laponite XLG), the mixture was heated to 80°C.
using an Ace homogenizer (Nippon Seiki)
The above range was obtained by stirring at 15000 rpm for 10 minutes to emulsify. Evaluation test 1 (when using stearic acid) Oil phase fixed paraffin 5.0 parts by weight Liquid paraffin 44.25-x Stearic acid x Water phase water 49.25 parts by weight Clay mineral Synthetic hectorite 1.5 parts by weight
【表】
○:良好 ×:分離または離漿
評価試験2(蜜ロウ(約14wt%の遊離脂肪酸含
有)使用時)油相
固形パラフイン 5.0重量部
流動パラフイン 44.25−x
蜜ロウ x 水相
水 49.25重量部粘土鉱物
合成ヘクトライト 1.5重量部[Table] ○: Good ×: Separation or syneresis evaluation test 2 (when using beeswax (containing about 14 wt% free fatty acids)) Oil phase solid paraffin 5.0 parts by weight Liquid paraffin 44.25−x Beeswax x aqueous phase water 49.25 parts by weight Part clay mineral Synthetic hectorite 1.5 parts by weight
【表】
○:良好 ×:分離または離漿
同様に、本発明者はゲル化能を有する粘土鉱物
の水相成分に対する割合を求めるようについて
は、次の評価試験3に示すように高級脂肪酸(ス
テアリン酸)を各々0.1重量%、1重量%、10重
量%の割合で溶解させた油相成分と水相成分とを
1:1(重量比)にし、これに合成へククトライ
ト(商品名ラポナイトXLG)の量を変化させて
混合した後、80℃にてユースホモゲナイザー(日
本精機)を用いて15000rpmの条件にて10分間撹
拌して乳化させたところ、上記の範囲を求め得た
ものである。
評価試験3(ステアリン酸1重量%の場合)油相組成
流動パラフイン 85重量%
固形パラフイン 14
ステアリン酸 1 水相組成
水 100重量%粘土鉱物
合成ヘクトライト[Table] ○: Good ×: Separation or syneresis Similarly, in order to determine the ratio of clay minerals with gelling ability to the aqueous phase components, the present inventors conducted higher fatty acids (as shown in the following evaluation test 3). Stearic acid) is dissolved at a ratio of 0.1%, 1%, and 10% by weight, respectively, to make the oil phase component and water phase component 1:1 (weight ratio). ) were mixed in varying amounts and emulsified by stirring at 15,000 rpm for 10 minutes at 80°C using a Youth Homogenizer (Nippon Seiki), and the above range was obtained. Evaluation test 3 (stearic acid 1% by weight) Oil phase composition Liquid paraffin 85% by weight Solid paraffin 14 Stearic acid 1 Water phase composition Water 100% by weight Clay mineral synthetic hectorite
【表】
○:良好、△:乳化不均一、×:分
離又は離漿
尚、ステアリン酸0.1wt%、10wt%の時も、結
果は表−3に同じ。
本発明に係る水中油型乳化組成物の新規な製造
法は、上記各成分を一定の条件において、混合、
強力撹拌することからなる製造法であり、各成分
の添加順序は問わないが、少なくとも良好な水中
油型乳化組成物を得るためには、高級脂肪酸と高
級脂肪酸含有物質とを油相成分中に充分に溶解さ
せておくと共に、各成分をPH4.0〜10.5の範囲に
調整しておくべきである。PH4.0未満ないしはPH
10.5以上ではゲル化が起こらず、従つていずれに
しても本発明の目的に適うものは得られない。PH
の調整は、選択される各種基剤の組合せにより行
なうが、必要ならば適量の酸、アルカリ等を用い
て行なつてもよい。
本発明の製造法は、詳細には、PH4.0〜10.5の
範囲になるように予め選択(または調整)した高
級脂肪酸もしくは高級脂肪酸含有物質を含む油相
成分、水相成分、ゲル化能を有する粘土鉱物等の
各成分を適宜の順序にて混合し、次いで70℃〜90
℃程度の高温好ましくは80℃前後にて、ホモゲナ
イザー、ホモミキサーなどの如き混合撹拌機で強
力に撹拌例えば5000〜20000rpm程度の範囲にお
いて5分〜30分撹拌し、得られるエマルジヨンを
冷却もしくは放冷してなる水中油型乳化組成物の
製造法に関するものである。この製造法における
強力な撹拌は油相成分をゲル中に細かく分散させ
るために必要である。また、温度範囲は添加され
るワツクス等の固形脂が充分に溶解する範囲が必
然的にとられる。
一般に、モンモリロナイト系粘土鉱物に属する
合成ヘクトライト(前述に同じ)は、化粧品分野
において、ゲル化剤またはゾル化剤として汎用さ
れている。化粧品原料の1つである。合成ヘクト
ライトは、水溶液に添加された際、一定の濃度以
上になると、水中でゲルを形成し、流動性を示さ
なくなる性質を有する。予めゲル形成が起つてい
るような合成ヘクトライト水溶液では、ゲル強度
が強くなると、油分をこれに添加しても、油分を
均一に分散させることは困難となる傾向がある。
本発明は、高級脂肪酸もしくは高級脂肪酸含有物
質と、水相成分と、合成ヘクトライトの三成分を
混合、攪拌すると、その攪拌中に界面活性剤に代
わるコンプレツクスが生じ、合成ヘクトライトと
水相全成分との間でゲル形成とエマルジヨン生成
とが同時に進行するため、結果的にゲル強度が保
持され、油分を均一に分散させることができる。
合成ヘクトライトは、従来ゲル化剤として化粧料
に用いられた例はあるが、このようなエマルジヨ
ン生成に寄与する目的で使用された例は皆無と云
つてよい。
本発明により得られる水中油型乳化組成物が界
面活性剤を使用していないため、皮膚刺激のなく
安全なものであるかを実証することを目的とし
て、後記実施例1の化粧料用水中油型乳化組成物
と、この処方中から合成ヘクトライトを除き各種
界面活性剤で置き換えて常法により製造した化粧
料用水中油型乳化組成物とを用い、全国健康成人
男子50名を対象として48時間人体パツチテストを
実施した。その結果、後者の市販品に相当する化
粧料用水中油型乳化組成物が高い陽性率を示した
のに対し、本発明に係る前者の化粧料用水中油型
乳化組成物はほとんど陽性は示さなかつた。
本発明に係る水中油型乳化組成物の製造法にお
いては、必要ならば、通常の乳化組成物の如く、
アミノ酸類、香料、防腐剤、色素、可塑剤、増粘
剤、中和剤、紫外線吸収剤、キレート剤等を用い
ることができる。また、本発明の目的に適した範
囲での界面活性剤の使用は許容される。
上記の如くして得られる水中油型乳化組成物特
に化粧料用水中油型乳化組成物は、皮膚刺激の殆
んどない安全なものであり、製造時における周到
な条件設定を必要とせずに均一な品質のものが得
られ、系の防腐ができ、経時による物理的特性の
変化はなく、乳化物の硬度などが温度に依存せ
ず、さつぱりとした使用感が得られるものであ
り、具体的には、ハンドクリーム、エモリエント
クリーム、フアンデーシヨン、キツチンクリーム
等のクリーム類の他、乳液類、パツク類等の乳化
形状を有するものであれば、高粘のものから流動
性の高い低粘性のものまで広く使用できる。ま
た、化粧料に問わず、軟膏基剤、食料品、塗料、
靴クリーム等各種の用途に使用できるものであ
る。
次に本発明水中油型乳化組成物の製造法の実施
例を述べる。尚、実施例中の数値は重量部を表わ
す。
実施例 1[Table] ○: Good, △: Non-uniform emulsification, ×: Separation or syneresis The results are the same as in Table 3 when stearic acid is 0.1wt% and 10wt%. The novel method for producing an oil-in-water emulsion composition according to the present invention includes mixing the above-mentioned components under certain conditions,
This is a production method that involves strong stirring, and the order of addition of each component does not matter, but in order to obtain at least a good oil-in-water emulsion composition, higher fatty acids and higher fatty acid-containing substances should be added to the oil phase components. In addition to sufficiently dissolving the ingredients, each component should be adjusted to a pH range of 4.0 to 10.5. PH less than 4.0 or PH
If it is 10.5 or more, gelation will not occur and therefore, in any case, it will not be possible to obtain a product suitable for the purpose of the present invention. PH
The adjustment is carried out by combining various bases selected, but if necessary, it may be carried out using an appropriate amount of acid, alkali, etc. In detail, the production method of the present invention uses an oil phase component containing a higher fatty acid or a higher fatty acid-containing substance, a water phase component, and a gelling ability that are selected (or adjusted) in advance to have a pH in the range of 4.0 to 10.5. Mix each component such as clay minerals in an appropriate order, and then heat at 70℃ to 90℃.
Stir vigorously using a mixer such as a homogenizer or a homomixer at a high temperature of about 80°C, preferably around 80°C. Stir for 5 to 30 minutes at a speed of about 5,000 to 20,000 rpm, and cool or leave to cool the resulting emulsion. The present invention relates to a method for producing an oil-in-water emulsion composition. Strong stirring in this production method is necessary to finely disperse the oil phase components into the gel. Further, the temperature range is necessarily set within a range in which solid fat such as wax to be added is sufficiently dissolved. In general, synthetic hectorite (same as above), which belongs to the montmorillonite clay mineral, is widely used as a gelling agent or solizing agent in the cosmetic field. It is one of the raw materials for cosmetics. When synthetic hectorite is added to an aqueous solution and the concentration exceeds a certain level, it forms a gel in water and exhibits no fluidity. In a synthetic hectorite aqueous solution in which gel formation has already occurred, when the gel strength becomes strong, it tends to be difficult to uniformly disperse the oil even if oil is added thereto.
In the present invention, when the three components of higher fatty acid or higher fatty acid-containing substance, aqueous phase component, and synthetic hectorite are mixed and stirred, a complex that replaces the surfactant is generated during the stirring, and the synthetic hectorite and the aqueous phase are mixed and stirred. Since gel formation and emulsion formation proceed simultaneously with all components, gel strength is maintained as a result, and oil can be uniformly dispersed.
Synthetic hectorite has been used as a gelling agent in cosmetics in the past, but it can be said that there have been no examples where it has been used for the purpose of contributing to the production of emulsions. In order to demonstrate whether the oil-in-water emulsion composition obtained by the present invention does not use a surfactant and is safe without skin irritation, the oil-in-water emulsion composition for cosmetics in Example 1 described below was prepared. Using an emulsified composition and an oil-in-water emulsified composition for cosmetics manufactured by a conventional method by removing synthetic hectorite from this formulation and replacing it with various surfactants, human bodies were tested for 48 hours on 50 healthy adult males nationwide. A patch test was conducted. As a result, the latter oil-in-water emulsion composition for cosmetics corresponding to a commercially available product showed a high positive rate, whereas the former oil-in-water emulsion composition for cosmetics according to the present invention hardly showed any positive results. . In the method for producing an oil-in-water emulsion composition according to the present invention, if necessary, like a normal emulsion composition,
Amino acids, fragrances, preservatives, pigments, plasticizers, thickeners, neutralizing agents, ultraviolet absorbers, chelating agents, etc. can be used. Further, the use of surfactants within a range suitable for the purpose of the present invention is permissible. The oil-in-water emulsion composition obtained as described above, especially the oil-in-water emulsion composition for cosmetics, is safe with almost no skin irritation, and is uniform without the need for careful setting of conditions during production. It is possible to obtain a product of good quality, it is possible to preserve the system, its physical properties do not change over time, the hardness of the emulsion does not depend on temperature, and it provides a refreshing feeling of use. Specifically, creams such as hand creams, emollient creams, foundations, and chitin creams, as well as emulsified products such as emulsions and packs, range from high viscosity to low fluidity. It can be used in a wide range of applications, even viscous ones. In addition, regardless of cosmetics, ointment bases, foodstuffs, paints,
It can be used for various purposes such as shoe cream. Next, an example of the method for producing the oil-in-water emulsion composition of the present invention will be described. In addition, the numerical values in the examples represent parts by weight. Example 1
【表】【table】
【表】
Aを70℃前後にて均一に約10分間溶解し、予め
調製しておいたBを添加した後、Cをこれに加え
て混合し、次いで温度70℃を保ち、10000rpmの
撹拌力にて10分間強力に撹拌し、得られるエマル
ジヨンを放冷し、Dを加えて目的とする水中油型
乳化組成物を得た。
実施例 2[Table] Dissolve A uniformly for about 10 minutes at around 70°C, add B prepared in advance, add C and mix, then maintain the temperature at 70°C and stir at 10,000 rpm. The resulting emulsion was stirred vigorously for 10 minutes, and the resulting emulsion was allowed to cool, and D was added to obtain the desired oil-in-water emulsion composition. Example 2
【表】
Aを70℃前後にて均一に約10分間溶解し、予め
調製しておいたBを添加した後、Cをこれに加え
て混合し、次いで温度70℃を保ち、10000rpmの
撹拌力にて10分間強力に撹拌し、得られるエマル
ジヨンを放冷し、Dを加えて目的とする水中油型
乳化組成物を得た。
実施例 3[Table] Dissolve A uniformly at around 70°C for about 10 minutes, add B prepared in advance, add C and mix, then maintain the temperature at 70°C and stir at 10,000 rpm. The resulting emulsion was stirred vigorously for 10 minutes, and the resulting emulsion was allowed to cool, and D was added to obtain the desired oil-in-water emulsion composition. Example 3
【表】【table】
【表】
Aを70℃前後にて均一に約10分間溶解し、予め
調製しておいたBを添加した後、Cをこれに加え
て混合し、次いで温度70℃を保ち、10000rpmの
撹拌力にて10分間強力に撹拌し、得られるエマル
ジヨンを放冷し、Dを加えて目的とする水中油型
乳化組成物を得た。
実施例 4[Table] Dissolve A uniformly for about 10 minutes at around 70°C, add B prepared in advance, add C and mix, then maintain the temperature at 70°C and stir at 10,000 rpm. The resulting emulsion was stirred vigorously for 10 minutes, and the resulting emulsion was allowed to cool, and D was added to obtain the desired oil-in-water emulsion composition. Example 4
【表】
Aを70℃前後にて均一に約10分間溶解し、予め
調製しておいたBを添加した後、Cをこれに加え
て混合し、次いで温度70℃を保ち、15000rpmの
撹拌力にて10分間強力に撹拌し、得られるエマル
ジヨンを放冷し、Dを加えて目的とする水中油型
乳化組成物を得た。[Table] Dissolve A uniformly at around 70°C for about 10 minutes, add B prepared in advance, add C and mix, then maintain the temperature at 70°C and stir at 15000 rpm. The resulting emulsion was stirred vigorously for 10 minutes, and the resulting emulsion was allowed to cool, and D was added to obtain the desired oil-in-water emulsion composition.
Claims (1)
質を含む油相成分5〜60重量%、水相成分40〜90
重量%、モンモリロナイト族粘土鉱物、ベントナ
イト及び合成雲母から選ばれる一種以上のゲル化
能を有する粘土鉱物0.5〜5重量%からなるPH4.0
〜10.5に調整された基剤成分において、該基剤成
分を混合し、次いで油相成分が溶解している温度
範囲下で強力に撹拌し、冷却する水中油型乳化組
成物の製造法。1 Oil phase component containing higher fatty acids and/or higher fatty acid-containing substances 5 to 60% by weight, water phase component 40 to 90% by weight
PH4.0 consisting of 0.5 to 5% by weight of a clay mineral having gelling ability of one or more types selected from montmorillonite group clay minerals, bentonite, and synthetic mica.
A method for producing an oil-in-water emulsion composition, which comprises mixing base components adjusted to a temperature of 10.5 to 10.5, followed by vigorous stirring in a temperature range in which the oil phase component is dissolved, and cooling.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP11437680A JPS5738936A (en) | 1980-08-20 | 1980-08-20 | Production of emulsified composition |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP11437680A JPS5738936A (en) | 1980-08-20 | 1980-08-20 | Production of emulsified composition |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS5738936A JPS5738936A (en) | 1982-03-03 |
JPS643529B2 true JPS643529B2 (en) | 1989-01-23 |
Family
ID=14636133
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP11437680A Granted JPS5738936A (en) | 1980-08-20 | 1980-08-20 | Production of emulsified composition |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS5738936A (en) |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP3273809B2 (en) * | 1992-06-29 | 2002-04-15 | 御木本製薬株式会社 | Oil-in-water cream base |
US5919398A (en) * | 1995-03-31 | 1999-07-06 | Shiseido Co., Ltd. | Oil-water mixed composition |
JP5483547B2 (en) * | 2009-11-11 | 2014-05-07 | 株式会社 資生堂 | Cosmetics |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS609853B2 (en) * | 1978-12-21 | 1985-03-13 | 日本サ−フアクタント工業株式会社 | Emulsion manufacturing method |
JPS56150007A (en) * | 1980-04-22 | 1981-11-20 | Kanebo Ltd | Creamy or milky skin cosmetic |
-
1980
- 1980-08-20 JP JP11437680A patent/JPS5738936A/en active Granted
Also Published As
Publication number | Publication date |
---|---|
JPS5738936A (en) | 1982-03-03 |
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