JPS59104308A - Pasty cosmetic for whitening skin color - Google Patents
Pasty cosmetic for whitening skin colorInfo
- Publication number
- JPS59104308A JPS59104308A JP57215339A JP21533982A JPS59104308A JP S59104308 A JPS59104308 A JP S59104308A JP 57215339 A JP57215339 A JP 57215339A JP 21533982 A JP21533982 A JP 21533982A JP S59104308 A JPS59104308 A JP S59104308A
- Authority
- JP
- Japan
- Prior art keywords
- higher fatty
- fatty acid
- oil
- ascorbic acid
- acid ester
- 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
- 239000002537 cosmetic Substances 0.000 title claims abstract description 31
- 230000002087 whitening effect Effects 0.000 title claims description 37
- 235000011837 pasties Nutrition 0.000 title 1
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 claims abstract description 70
- 235000014113 dietary fatty acids Nutrition 0.000 claims abstract description 45
- 229930195729 fatty acid Natural products 0.000 claims abstract description 45
- 239000000194 fatty acid Substances 0.000 claims abstract description 45
- -1 fatty acid ester Chemical class 0.000 claims abstract description 44
- 235000010323 ascorbic acid Nutrition 0.000 claims abstract description 34
- 239000011668 ascorbic acid Substances 0.000 claims abstract description 34
- 229960005070 ascorbic acid Drugs 0.000 claims abstract description 34
- 239000007788 liquid Substances 0.000 claims abstract description 29
- 239000003921 oil Substances 0.000 claims abstract description 23
- 235000019198 oils Nutrition 0.000 claims abstract description 23
- 150000004665 fatty acids Chemical class 0.000 claims abstract description 7
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract description 7
- 239000004006 olive oil Substances 0.000 claims abstract description 6
- 235000008390 olive oil Nutrition 0.000 claims abstract description 6
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 4
- 150000002148 esters Chemical class 0.000 claims description 6
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 4
- 239000004615 ingredient Substances 0.000 claims description 3
- ALSTYHKOOCGGFT-KTKRTIGZSA-N (9Z)-octadecen-1-ol Chemical compound CCCCCCCC\C=C/CCCCCCCCO ALSTYHKOOCGGFT-KTKRTIGZSA-N 0.000 claims description 2
- 235000019489 Almond oil Nutrition 0.000 claims description 2
- CMBYOWLFQAFZCP-UHFFFAOYSA-N Hexyl dodecanoate Chemical compound CCCCCCCCCCCC(=O)OCCCCCC CMBYOWLFQAFZCP-UHFFFAOYSA-N 0.000 claims description 2
- 241000772415 Neovison vison Species 0.000 claims description 2
- 235000019485 Safflower oil Nutrition 0.000 claims description 2
- 239000008168 almond oil Substances 0.000 claims description 2
- 235000021302 avocado oil Nutrition 0.000 claims description 2
- 239000008163 avocado oil Substances 0.000 claims description 2
- SASYSVUEVMOWPL-NXVVXOECSA-N decyl oleate Chemical compound CCCCCCCCCCOC(=O)CCCCCCC\C=C/CCCCCCCC SASYSVUEVMOWPL-NXVVXOECSA-N 0.000 claims description 2
- SFFVATKALSIZGN-UHFFFAOYSA-N hexadecan-7-ol Chemical compound CCCCCCCCCC(O)CCCCCC SFFVATKALSIZGN-UHFFFAOYSA-N 0.000 claims description 2
- 229940100463 hexyl laurate Drugs 0.000 claims description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 2
- 229940119170 jojoba wax Drugs 0.000 claims description 2
- 229940105132 myristate Drugs 0.000 claims description 2
- 229940055577 oleyl alcohol Drugs 0.000 claims description 2
- XMLQWXUVTXCDDL-UHFFFAOYSA-N oleyl alcohol Natural products CCCCCCC=CCCCCCCCCCCO XMLQWXUVTXCDDL-UHFFFAOYSA-N 0.000 claims description 2
- 235000005713 safflower oil Nutrition 0.000 claims description 2
- 239000003813 safflower oil Substances 0.000 claims description 2
- 239000008159 sesame oil Substances 0.000 claims description 2
- 235000011803 sesame oil Nutrition 0.000 claims description 2
- TUNFSRHWOTWDNC-UHFFFAOYSA-N tetradecanoic acid Chemical compound CCCCCCCCCCCCCC(O)=O TUNFSRHWOTWDNC-UHFFFAOYSA-N 0.000 claims description 2
- TUYRNAGGIJZRNM-LBHUVFDKSA-N [(2s)-2-[(2r)-4-hexadecanoyloxy-3-hydroxy-5-oxo-2h-furan-2-yl]-2-hydroxyethyl] hexadecanoate Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](O)[C@H]1OC(=O)C(OC(=O)CCCCCCCCCCCCCCC)=C1O TUYRNAGGIJZRNM-LBHUVFDKSA-N 0.000 claims 1
- 150000001875 compounds Chemical class 0.000 claims 1
- UVPGECJLXBGLDW-UHFFFAOYSA-N octadecan-7-ol Chemical compound CCCCCCCCCCCC(O)CCCCCC UVPGECJLXBGLDW-UHFFFAOYSA-N 0.000 claims 1
- 229940116351 sebacate Drugs 0.000 claims 1
- CXMXRPHRNRROMY-UHFFFAOYSA-L sebacate(2-) Chemical compound [O-]C(=O)CCCCCCCCC([O-])=O CXMXRPHRNRROMY-UHFFFAOYSA-L 0.000 claims 1
- 229920000223 polyglycerol Polymers 0.000 abstract 3
- RZVAJINKPMORJF-UHFFFAOYSA-N Acetaminophen Chemical compound CC(=O)NC1=CC=C(O)C=C1 RZVAJINKPMORJF-UHFFFAOYSA-N 0.000 abstract 1
- 150000002194 fatty esters Chemical class 0.000 abstract 1
- 239000002253 acid Substances 0.000 description 10
- 239000006072 paste Substances 0.000 description 8
- 239000000047 product Substances 0.000 description 8
- 230000000694 effects Effects 0.000 description 7
- GPLRAVKSCUXZTP-UHFFFAOYSA-N diglycerol Chemical compound OCC(O)COCC(O)CO GPLRAVKSCUXZTP-UHFFFAOYSA-N 0.000 description 5
- 235000019197 fats Nutrition 0.000 description 5
- 238000000034 method Methods 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- 229940105990 diglycerin Drugs 0.000 description 4
- XDOFQFKRPWOURC-UHFFFAOYSA-N 16-methylheptadecanoic acid Chemical compound CC(C)CCCCCCCCCCCCCCC(O)=O XDOFQFKRPWOURC-UHFFFAOYSA-N 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- WNWHHMBRJJOGFJ-UHFFFAOYSA-N 16-methylheptadecan-1-ol Chemical compound CC(C)CCCCCCCCCCCCCCCO WNWHHMBRJJOGFJ-UHFFFAOYSA-N 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- YZXBAPSDXZZRGB-DOFZRALJSA-N arachidonic acid Chemical compound CCCCC\C=C/C\C=C/C\C=C/C\C=C/CCCC(O)=O YZXBAPSDXZZRGB-DOFZRALJSA-N 0.000 description 2
- 230000008859 change Effects 0.000 description 2
- 239000008300 cosmetic paste Substances 0.000 description 2
- 239000006071 cream Substances 0.000 description 2
- 239000013078 crystal 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
- 235000019441 ethanol Nutrition 0.000 description 2
- XMHIUKTWLZUKEX-UHFFFAOYSA-N hexacosanoic acid Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCC(O)=O XMHIUKTWLZUKEX-UHFFFAOYSA-N 0.000 description 2
- 235000015110 jellies Nutrition 0.000 description 2
- 239000008274 jelly Substances 0.000 description 2
- 239000006210 lotion Substances 0.000 description 2
- 230000009467 reduction Effects 0.000 description 2
- 238000003860 storage Methods 0.000 description 2
- 238000010998 test method Methods 0.000 description 2
- OYHQOLUKZRVURQ-NTGFUMLPSA-N (9Z,12Z)-9,10,12,13-tetratritiooctadeca-9,12-dienoic acid Chemical compound C(CCCCCCC\C(=C(/C\C(=C(/CCCCC)\[3H])\[3H])\[3H])\[3H])(=O)O OYHQOLUKZRVURQ-NTGFUMLPSA-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
- ZONJATNKKGGVSU-UHFFFAOYSA-N 14-methylpentadecanoic acid Chemical compound CC(C)CCCCCCCCCCCCC(O)=O ZONJATNKKGGVSU-UHFFFAOYSA-N 0.000 description 1
- YEGNTQBFSQBGJT-UHFFFAOYSA-N 2-heptylundecan-1-ol Chemical compound CCCCCCCCCC(CO)CCCCCCC YEGNTQBFSQBGJT-UHFFFAOYSA-N 0.000 description 1
- BGRXBNZMPMGLQI-UHFFFAOYSA-N 2-octyldodecyl tetradecanoate Chemical compound CCCCCCCCCCCCCC(=O)OCC(CCCCCCCC)CCCCCCCCCC BGRXBNZMPMGLQI-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
- OEOIWYCWCDBOPA-UHFFFAOYSA-N 6-methyl-heptanoic acid Chemical compound CC(C)CCCCC(O)=O OEOIWYCWCDBOPA-UHFFFAOYSA-N 0.000 description 1
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
- 240000002234 Allium sativum Species 0.000 description 1
- 235000017166 Bambusa arundinacea Nutrition 0.000 description 1
- 235000017491 Bambusa tulda Nutrition 0.000 description 1
- 235000021357 Behenic acid Nutrition 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- ZZZCUOFIHGPKAK-UHFFFAOYSA-N D-erythro-ascorbic acid Natural products OCC1OC(=O)C(O)=C1O ZZZCUOFIHGPKAK-UHFFFAOYSA-N 0.000 description 1
- 102000004190 Enzymes Human genes 0.000 description 1
- 108090000790 Enzymes Proteins 0.000 description 1
- 206010014970 Ephelides Diseases 0.000 description 1
- 239000005639 Lauric acid Substances 0.000 description 1
- 208000003351 Melanosis Diseases 0.000 description 1
- 240000007817 Olea europaea Species 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
- 244000082204 Phyllostachys viridis Species 0.000 description 1
- 235000015334 Phyllostachys viridis Nutrition 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- 229930003268 Vitamin C Natural products 0.000 description 1
- LDDUCKDUDZVHLN-UHFFFAOYSA-N [2-hydroxy-3-[2-hydroxy-3-(16-methylheptadecanoyloxy)propoxy]propyl] 16-methylheptadecanoate Chemical compound CC(C)CCCCCCCCCCCCCCC(=O)OCC(O)COCC(O)COC(=O)CCCCCCCCCCCCCCC(C)C LDDUCKDUDZVHLN-UHFFFAOYSA-N 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 230000004913 activation Effects 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 229940114079 arachidonic acid Drugs 0.000 description 1
- 235000021342 arachidonic acid Nutrition 0.000 description 1
- 125000003289 ascorbyl group Chemical group [H]O[C@@]([H])(C([H])([H])O*)[C@@]1([H])OC(=O)C(O*)=C1O* 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 239000011425 bamboo Substances 0.000 description 1
- 229940116226 behenic acid Drugs 0.000 description 1
- 230000004098 cellular respiration Effects 0.000 description 1
- 238000006243 chemical reaction Methods 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
- 238000013329 compounding Methods 0.000 description 1
- 239000007859 condensation product Substances 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 238000004925 denaturation Methods 0.000 description 1
- 230000036425 denaturation Effects 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 239000010696 ester oil Substances 0.000 description 1
- OBNCKNCVKJNDBV-UHFFFAOYSA-N ethyl butyrate Chemical compound CCCC(=O)OCC OBNCKNCVKJNDBV-UHFFFAOYSA-N 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 239000003205 fragrance Substances 0.000 description 1
- 235000004611 garlic Nutrition 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- IPCSVZSSVZVIGE-UHFFFAOYSA-M hexadecanoate Chemical compound CCCCCCCCCCCCCCCC([O-])=O IPCSVZSSVZVIGE-UHFFFAOYSA-M 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 239000002932 luster Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 238000000691 measurement method Methods 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229910021645 metal ion Inorganic materials 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- 229940073665 octyldodecyl myristate Drugs 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 230000033116 oxidation-reduction process Effects 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 230000000630 rising effect Effects 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 230000035807 sensation Effects 0.000 description 1
- 231100000245 skin permeability Toxicity 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 229960004274 stearic acid Drugs 0.000 description 1
- TUNFSRHWOTWDNC-HKGQFRNVSA-N tetradecanoic acid Chemical compound CCCCCCCCCCCCC[14C](O)=O TUNFSRHWOTWDNC-HKGQFRNVSA-N 0.000 description 1
- LOIYMIARKYCTBW-OWOJBTEDSA-N trans-urocanic acid Chemical compound OC(=O)\C=C\C1=CNC=N1 LOIYMIARKYCTBW-OWOJBTEDSA-N 0.000 description 1
- LOIYMIARKYCTBW-UHFFFAOYSA-N trans-urocanic acid Natural products OC(=O)C=CC1=CNC=N1 LOIYMIARKYCTBW-UHFFFAOYSA-N 0.000 description 1
- 238000005809 transesterification reaction Methods 0.000 description 1
- 150000005691 triesters Chemical class 0.000 description 1
- 210000002700 urine Anatomy 0.000 description 1
- 229940088594 vitamin Drugs 0.000 description 1
- 229930003231 vitamin Natural products 0.000 description 1
- 235000013343 vitamin Nutrition 0.000 description 1
- 239000011782 vitamin Substances 0.000 description 1
- 235000019155 vitamin A Nutrition 0.000 description 1
- 239000011719 vitamin A Substances 0.000 description 1
- 235000019154 vitamin C Nutrition 0.000 description 1
- 239000011718 vitamin C Substances 0.000 description 1
- 235000019166 vitamin D Nutrition 0.000 description 1
- 239000011710 vitamin D Substances 0.000 description 1
- 230000037303 wrinkles Effects 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
- A61K8/67—Vitamins
- A61K8/676—Ascorbic acid, i.e. vitamin C
-
- 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
- A61K8/39—Derivatives containing from 2 to 10 oxyalkylene groups
-
- 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
- A61K8/49—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds
- A61K8/4973—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with oxygen as the only hetero atom
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q17/00—Barrier preparations; Preparations brought into direct contact with the skin for affording protection against external influences, e.g. sunlight, X-rays or other harmful rays, corrosive materials, bacteria or insect stings
- A61Q17/04—Topical preparations for affording protection against sunlight or other radiation; Topical sun tanning preparations
-
- 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
- A61Q19/02—Preparations for care of the skin for chemically bleaching or whitening the skin
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Birds (AREA)
- Epidemiology (AREA)
- Dermatology (AREA)
- Emergency Medicine (AREA)
- Cosmetics (AREA)
Abstract
Description
【発明の詳細な説明】
本発明は、アスコルビン酸高級脂肪酸エステルが液状の
ポリグリセリン側鎖脂肪酸エステルー液状油の混合系に
均一に溶解していて非結晶性のペースト状を形成してお
シ、そして外観が均質で光沢をMしかつ安定性に優れ、
使用時には良好な美白効果と感一瞥え得る新規なペース
ト状の美白化粧料に関する。DETAILED DESCRIPTION OF THE INVENTION The present invention is characterized in that ascorbic acid higher fatty acid ester is uniformly dissolved in a mixed system of liquid polyglycerin side chain fatty acid ester and liquid oil to form an amorphous paste. It has a homogeneous appearance, high gloss, and excellent stability.
The present invention relates to a novel paste-like whitening cosmetic that has a good whitening effect and a visible sensation when used.
従来、アスコルビン酸やそのエステルは、強い酸化還元
作用によシ細胞呼吸作用、酵素紙活作用、膠原形作用等
を有し、かつメラニン還元作用によシ美白化粧料中に配
合使用されている,しかしながら、アスコルビン酸は光
、熱、酸素、金属イオン、PH等によシ分解し易く、安
定性に乏しいために美白効果の低下、ビタミンC作用の
低下、副作用等を起す欠点かある。Conventionally, ascorbic acid and its esters have been used in whitening cosmetics because of their strong oxidation-reduction effects, which have cellular respiration, enzyme paper activation, and collagen-forming effects, and because of their melanin-reducing effects. However, ascorbic acid is easily decomposed by light, heat, oxygen, metal ions, PH, etc., and has poor stability, resulting in a reduction in whitening effect, a reduction in vitamin C action, and side effects.
一方、アスコルビン酸高級脂肪酸エステルは,エチルア
ルコール、水、塩基性物質を含有する系(クリーム、ロ
ーシ冒ン等)の中では、加水分解、エステル交換等の反
応を起して変性し、着色したシ美白効果を低下する。こ
れらの欠点を改良するために、1−ヒドロキシエタン−
1.1−ジフオスホン酸(塩)等の多くの安定化剤が開
発されているか、前記の如き混合系中では、長期保存す
ると着色や美白効果を低下を起しやすく、満足し得るも
のは殆んど見出されていない。アスコルビン酸高級脂肪
酸エステルを安定にかつ溶解するために水、アルコール
等を含有しない油性基剤に溶解させて使用することも考
えられるが、該エステル油は液状油に溶解し難く、加熱
溶解しても冷却、放置すると白濁、沈澱、再結晶化等を
起しやすい。On the other hand, ascorbic acid higher fatty acid esters undergo reactions such as hydrolysis and transesterification, resulting in denaturation and coloration in systems containing ethyl alcohol, water, and basic substances (cream, lotion paste, etc.). Decreases wrinkle whitening effect. In order to improve these drawbacks, 1-hydroxyethane-
1. Many stabilizers such as 1-diphosphonic acid (salt) have been developed, but in the mixed system as mentioned above, long-term storage tends to cause coloring and whitening effects, and most of them are not satisfactory. It hasn't been discovered yet. In order to stabilize and dissolve ascorbic acid higher fatty acid ester, it is possible to use it by dissolving it in an oily base that does not contain water, alcohol, etc. However, the ester oil is difficult to dissolve in liquid oil, and it is difficult to dissolve it by heating. If it is cooled or left unattended, clouding, precipitation, recrystallization, etc. are likely to occur.
まだ適当な可溶化剤や乳化剤も現存しない。There are currently no suitable solubilizers or emulsifiers.
更に、アスコルビン酸やそのエステルの粉末を配合した
パウダー状の美白化粧料は比較的安定であるが、ローシ
ョンやクリームに分赦して使用するのに手間がかかシ、
皮膚への浸透性、速効性に乏しい。Furthermore, powdered whitening cosmetics containing powdered ascorbic acid or its esters are relatively stable, but they require a lot of effort to mix into lotions and creams.
Poor skin permeability and fast-acting properties.
本発明の目的はアスコルビン酸高級脂肪酸エステルが、
液状のポリグリセリン側鎖高級脂肪酸エステルー液状油
の混合系に均一に溶解しておυ、そして外観が均質で、
光沢を有し、安定性に優れ、使用時には肌に速効的に作
用して、優れた美白効果と、良好な感触及び撥水性を与
え得るペースト状の美白化粧料を提供することニアル。The object of the present invention is that ascorbic acid higher fatty acid ester is
It is uniformly dissolved in a mixed system of liquid polyglycerin side chain higher fatty acid ester and liquid oil, and has a homogeneous appearance.
To provide a paste-like whitening cosmetic that has luster, excellent stability, acts quickly on the skin during use, and can provide an excellent whitening effect, good touch, and water repellency.
ヶユ)VtX(R’35丞ユ惧4?戸閂蒜.すなわち、
本発明はアスコルヒノ酸尚級脂肪酸エステルと液状のポ
リグリセリン側鎖島級脂肪酸エステルと液状油とからな
ることを特徴とするペースト状の美白化粧料である。Kayu) VtX (R'35 丞ゆう 4? Tobari Garlic. In other words,
The present invention is a whitening cosmetic in the form of a paste, which is characterized by comprising an ascolhinoic acid lower fatty acid ester, a liquid polyglycerin side chain island class fatty acid ester, and a liquid oil.
以下、本発明の実施の態様を詳説する。Hereinafter, embodiments of the present invention will be explained in detail.
本発明に使用するアスコルビン酸高級脂訪酸エステルは
、アスコルピンと高級脂肪酸から成るモノエステル、シ
エステル、トリエステル等であって、そのエステルの酸
部分としては、例えは、ラウリン酸、ミリスチン酸、バ
ルミチン酸、ステアリン酸、アラキドン酸、ベヘニン酸
、セロチン酸、オレイン酸、リノール酸等である。The ascorbic acid higher fatty acid esters used in the present invention are monoesters, siesters, triesters, etc. consisting of ascorpine and higher fatty acids, and the acid moiety of the ester is, for example, lauric acid, myristic acid, valmitinic acid, etc. acids, stearic acid, arachidonic acid, behenic acid, cerotic acid, oleic acid, linoleic acid, etc.
それらの中で、アスコルビン酸モノステアレート、アス
コルビ/酸モノバルミテート、アスコルピン酸モノオレ
ート、アスコルビン酸ジステアレート、アスコルピン酸
シハルミテート、アスコルピン酸トリバルミテート等が
入手し易い等の点で好ましいものである。Among them, ascorbic acid monostearate, ascorbyl/acid monobalmitate, ascorbic acid monooleate, ascorbic acid distearate, ascorbic acid cyhalmitate, ascorbic acid tribalmitate, etc. are preferred because they are easily available.
アスコルピン酸高級脂肪酸エステルは一種または二種以
上組合せて使用される。アスコルビン酸高級脂肪酸エス
テルの使用量(配合量)は、処方成分の全量(当該化粧
料)重量に対して6〜40重瀘%、好ましくは8〜20
重量%である。6重量%よシも少なくなると、製品の粘
度が低くなって目的のペーストの美白化粧料を形成し難
く、また40重量%よりも多くなるとアスコルビン酸高
級脂1シ冨t品が遊離生成して均質でかつ光沢のある良
好な外観を与え難く、かつ肌にざらつくようなわるい感
触を与える等して好ましくない。Ascorbic acid higher fatty acid esters may be used alone or in combination. The amount of ascorbic acid higher fatty acid ester used (compounding amount) is 6 to 40% by weight, preferably 8 to 20% by weight, based on the total weight of the prescription ingredients (the cosmetic).
Weight%. When it is less than 6% by weight, the viscosity of the product becomes low and it is difficult to form the desired whitening cosmetic paste, and when it is more than 40% by weight, ascorbic acid high fat products are produced freely. It is undesirable because it is difficult to give a good, homogeneous and glossy appearance, and it also gives a rough and unpleasant feel to the skin.
本発明に使用する液状のポリグリセリン高級脂肪酸エス
テルとしては、グリセリンの自己縮合物であるポリグリ
セリン(ジグリセリン、トリグリセリン、テトラグリセ
リン、ペンタクリセリン、ヘキサグリセリン、ヘブタグ
リセリン、オクダグリセリン、ノナグリセリン、デカグ
リセリン等)と炭素数8以上の側鎖を有する高級脂肪酸
とのエステル化反応によって生成する部分エステル化物
か望ましい。The liquid polyglycerin higher fatty acid ester used in the present invention includes polyglycerin which is a self-condensation product of glycerin (diglycerin, triglycerin, tetraglycerin, pentacrycerin, hexaglycerin, hebutaglycerin, ocdaglycerin, nonaglycerin). , decaglycerin, etc.) and a higher fatty acid having a side chain of 8 or more carbon atoms.
例えは下記の式
(式中でRは、水素原子または炭素数8以上の側鎖高級
脂肪酸残基である。ただし、Ri−1:、1分子当シ2
個以上水素原子であるが全部が水素原子であることかな
い。nは。または1〜8である,上記の側鎖高級脂肪酸
残基における当該側鎖高級脂肪酸としては、例えば、イ
ソオクタン酸、インデカン酸、インドデヵン酸一イノミ
リスチン酸、イソパルミチン酸、イソステアリン酸等が
好ましい。An example is the following formula (in the formula, R is a hydrogen atom or a side chain higher fatty acid residue having 8 or more carbon atoms.
There are more than 1 hydrogen atoms, but they cannot all be hydrogen atoms. n is. As the side chain higher fatty acid in the above side chain higher fatty acid residue which is 1 to 8, for example, isooctanoic acid, indecanoic acid, indodecanoic acid, monoinomiristic acid, isopalmitic acid, isostearic acid, etc. are preferable.
また上記のポリグリセリンとしては、例えばジグリセリ
ン、トリグリセリン、テトラグリセリン、ペンタグリセ
リン、ノナグリセリン、オクタグリ犬り/、デカグリセ
リン、ヘキサグリセリンであることが好ましい。ジグリ
セリンである場合は、感触の良好な(ベタっき感が少な
く、禰度が低い》ペースト状の美白化粧料を調製(処方
設計)しやすい等の点で最も好ましい。Preferable examples of the polyglycerin include diglycerin, triglycerin, tetraglycerin, pentaglycerin, nonaglycerin, octaglycerin, decaglycerin, and hexaglycerin. In the case of diglycerin, it is most preferable because it is easy to prepare (formulate) a paste-like whitening cosmetic that has a good feel (less sticky feeling and low greasiness).
該ポリグリヒリン側鎖高級脂肪酸エステルは、その分子
中に少なくとも二つ以上の遊−J−Of{基が残存した
、部分エステルであることは好まし/i′
ζ一′一
い。か\る部エス1ルであると前記アスコルビン酸高級
脂肪酸エステルの溶解性が高まフ、美麗な外観を有し、
保存時の安定性、使用時の美白効果や感触、而1水性に
優れたペースト状美白化粧料が得られやすく、好ましい
。The polyglychlin side chain higher fatty acid ester is preferably a partial ester in which at least two or more free -J-Of{ groups remain in the molecule. When the part is S1, the solubility of the ascorbic acid higher fatty acid ester increases and it has a beautiful appearance.
It is preferable because it is easy to obtain a paste-like whitening cosmetic that has excellent stability during storage, whitening effect and feel during use, and 1) aqueous properties.
ポリグリセリン側鎖高級脂肪酸エステルの使用量は、該
組成♂績7冫重量に対して40〜90重量%、好ましく
は60〜85重量%である,40重量%よシも少なくな
ると、アスコルビン酸高級脂肪酸エステルの結晶が析出
しやすくなるO
次に液状油としては、化粧料に使用される常温下で液状
の油性物質(例えはエステル油、高級アルコール、Vm
W物油、炭化水累油)t−使用し得るが、例えばアーモ
ンド油、オリーブ油、ゴマ油、サフラワー油、ミンク油
、アボカド油、ホホバ油、イソブロビルミリステート、
イソブロビルパルミテート、オクチルドデシルミリステ
ート、イングロビルイソステアレート、デシルオレート
、ヘキシルラウレート、ジイノブロ、ピルアジペート、
ジイソプ口ピルセパヶート、オレイルアルコール、イソ
ステアリルアルコール、;rクチルドデヵノール、ヘキ
シルデヵノールーへプチルウンデヵノール等が、好まし
いものである。The amount of the polyglycerin side chain higher fatty acid ester used is 40 to 90% by weight, preferably 60 to 85% by weight, based on the weight of the composition. Crystals of fatty acid esters tend to precipitate.
(Water oil, hydrocarbon oil) may be used, such as almond oil, olive oil, sesame oil, safflower oil, mink oil, avocado oil, jojoba oil, isobrobyl myristate,
Isobrobyl palmitate, octyldodecyl myristate, inglovir isostearate, decyl oleate, hexyl laurate, diinobro, pyradipate,
Preferred are diisopropylseparate, oleyl alcohol, isostearyl alcohol, ctyldodecanol, hexyldecanol, heptylundecanol, and the like.
処方族竹Q企里
液状油の使用量は、該組成ThlDJtttK′対し、
4〜50重崖%、好1しくは1o〜30重量%である。The amount of formula family Bamboo Q Kiri liquid oil to be used is based on the composition ThlDJtttK'.
It is 4 to 50% by weight, preferably 10 to 30% by weight.
4重量%よシも少なくなるとべたつき感が増して好捷し
くない。If the amount is less than 4% by weight, the sticky feeling increases and is not pleasant.
”’Offi量%よクも多くなると、アスコルビン酸高
級脂肪酸エステルの結晶が析出しゃすくなク、光沢のあ
る均質な外観の製品が得難くなる傾向がある。``When the Offi amount % increases, crystals of ascorbic acid higher fatty acid ester tend to precipitate, making it difficult to obtain a product with a glossy and homogeneous appearance.
本発明に使用される慣用添加成分としては香料、着色材
を挙けることができるか、必要に応じてビタミンA,D
等のビタミン類、ウロカニン酸等の公知の,k外+m吸
収剤を添加しても艮い@本発明のペースト状美白化粧料
は液状のポリグリセリン側鎖(分岐)高級脂肪酸エステ
ルー液状油の混合系中に均一にa解しておυ、そして外
観が均質で元ν<をMし、安定性に優れ、使用時には肌
に過度速効的に作用L一で、優れた美白効果と良好な感
触及び撥水性を与え得る等、その作用効果は著しく、商
品価値は極めて関い。Conventional additive ingredients used in the present invention include fragrances, colorants, and vitamins A and D as needed.
Vitamins such as, urocanic acid, and other known K+M absorbers may be added. The paste whitening cosmetic of the present invention is a mixture of liquid polyglycerin side chain (branched) higher fatty acid ester and liquid oil. It is uniformly dissolved in the system, has a homogeneous appearance, has an original value of ν, has excellent stability, has an extremely rapid effect on the skin when used, has an excellent whitening effect, and has a good texture. Its effects are remarkable, such as providing water repellency, and its commercial value is extremely important.
以下、本発明の実施例について説明する。Examples of the present invention will be described below.
実施例に示す%とは重一%、部とは重j部を意味する。In the Examples, % means 1% by weight, and parts means j parts by weight.
なお、感触、大白効果、安足性については後述の方法で
調べた。The feel, white effect, and foot comfort were examined using the methods described below.
(υ感触
専門検査員20人によって実用テストを実施し、べたつ
き感Q〕有無t調べた。(A practical test was carried out by 20 testers specializing in the feel of the product, and the presence or absence of a sticky feeling Q) was investigated.
(2)光沢
JIS−Z8741−1962の光沢贋測定方法の方法
2に準じた。(2) Gloss According to method 2 of the gloss counterfeit measurement method of JIS-Z8741-1962.
油脂分析試験法ガードナー法に準じた。Based on the Gardner method for oil and fat analysis.
(4)美白効果
色黒、しみ、そばかすを有する女性10名に対して試料
を朝夕3ケ月間毎日顔面に塗布し、美白効果有りと答え
た人数を調査した。(4) Whitening effect Samples were applied to the faces of 10 women with dark skin, age spots, and freckles every morning and evening for 3 months for 3 months, and the number of people who answered that the product had a whitening effect was investigated.
(5)硬度
感圧軸5.6/、スプリング100gr,ウェイト10
0lr,上昇速度ηインチ/秒のカードテンションメー
ターを用いて測定した。(5) Hardness pressure sensitive shaft 5.6/, spring 100gr, weight 10
Measurements were made using a card tension meter with a rising speed of η inch/sec.
(術生試験法1965年香粧品試験法B.2.(2).
硬度、カードテンノヨンメーター法に準ずる。)
実施例1
(1)処方
1.オリーブ油15部
2.ブスコルビ/酸モノステアレート10部6ポリグリ
セリン側鎖脂肪酸エステル75部(表−1に示したもの
)
(2)製造
上記成分の2及び3を油浴中で100℃まで加熱し、均
一に溶解した後、冷やした金属バットに流し込んで急冷
する。(Articles Test Method 1965 Cosmetics Test Method B.2.(2).
Hardness, according to the Card Tennoyon meter method. ) Example 1 (1) Prescription 1. 15 parts olive oil2. Buscorby/acid monostearate 10 parts 6 Polyglycerin side chain fatty acid ester 75 parts (as shown in Table 1) (2) Production Heat the above components 2 and 3 to 100°C in an oil bath and dissolve them uniformly. After that, pour it into a cold metal vat and let it cool down quickly.
次いでこのペーストと上記成分の1をローラーで混ぜて
本発明のペースト状の美白化粧料を調魁した。Next, this paste and the above-mentioned component 1 were mixed with a roller to prepare a paste-like whitening cosmetic composition of the present invention.
(3)製品の特性
表−1の結果からも明らかなようしこ、堵に発明のペー
スト状美白化粧料は・感触・光沢・色調、美白効果及び
アスコノレビン酸モノステアレートの安定性が良好であ
・ふ。一−一比較例1〜比較卸6
ポリグリセリン側61ill肪酸エステルの代υに、表
−2に示す液状物質の夫々を使用する他は、実施例1と
同,尿に行なった。その結果を表−2に示した。(3) Product Characteristics It is clear from the results in Table 1 that the paste whitening cosmetic of the invention has good feel, gloss, color tone, whitening effect, and stability of asconolebic acid monostearate. Ah, huh. 1-1 Comparative Examples 1 to 6 The same procedure as in Example 1 was conducted for urine, except that each of the liquid substances shown in Table 2 was used in place of the 61ill fatty acid ester on the polyglycerin side. The results are shown in Table-2.
呵施例2
ポリグリセリン側鎖脂肪酸エステルとしてジグリセリン
ジイソステアレート、アスコルビン酸高級脂′肪酪エス
テルとして表−3の如く種々変化さす他は,実施例1と
同様にしてペースト状美白化粧料を調製[5た。(2) Example 2 A paste whitening cosmetic was prepared in the same manner as in Example 1, except that diglycerin diisostearate was used as the polyglycerin side chain fatty acid ester and various changes were made as shown in Table 3 as ascorbic acid higher fat butyric ester. was prepared [5.
表=乙の結果から明らかな如く、本発明におーて辿猟の
アスコルピン酸高級脂肪酸エステルを使用すれば、感触
、光沢に優れ、色訴等の経時変化の少ないペースト状美
白化粧料が得られる0/r)
実施例3
アスコルピン酸モノステアレートの配合量を表−4の如
く変化し、ポリグリセリン側鎖脂肪酸エステルとして、
ジグリセリンジインステアレートを用いる他は、実施例
1と同様Kしてぺ一スト状美白化粧料を調製した。As is clear from the results in Table B, by using the ascorbic acid higher fatty acid ester of the present invention, it is possible to obtain a paste-like whitening cosmetic that has excellent feel and gloss, and has little change over time such as color complaints. Example 3 The blending amount of ascorbic acid monostearate was changed as shown in Table 4, and as polyglycerin side chain fatty acid ester,
A paste-like whitening cosmetic was prepared in the same manner as in Example 1, except that diglycerine diinstearate was used.
表−4から明らかな如く、本発明のアスコルビン酸高級
脂肪酸エステルの配合量は6〜40重量%である。6重
量%よ多少ないと製品の粘度が低く目的のペースト状美
白化粧料が得られない0
又、40重景%よシも多くなると該エステルが再結晶し
,、光沢のある均質な外観の製品が得られな“・,、.
乙二゛\,
実施例4
ポリグリセリン側鎖脂肪酸エステルとして表一5に示し
たものを使用する他は実施例1と同様にしてペースト状
美白化粧料を調製した。As is clear from Table 4, the amount of ascorbic acid higher fatty acid ester of the present invention is 6 to 40% by weight. If it is less than 6% by weight, the viscosity of the product is low and the desired paste-like whitening cosmetic cannot be obtained.In addition, if it is more than 40% by weight, the ester recrystallizes, resulting in a glossy, homogeneous appearance. I can't get the product...
Example 4 A paste whitening cosmetic was prepared in the same manner as in Example 1, except that the polyglycerin side chain fatty acid ester shown in Table 15 was used.
表−5から明らかな如く、小リグリセリン側鎖脂肪酸エ
ステルとしてはその分子内に二つ以上のOH基が残存す
るグリセリン側鎚脂肪酸である事が好ましい。As is clear from Table 5, the small glycerin side chain fatty acid ester is preferably a glycerin side chain fatty acid in which two or more OH groups remain in the molecule.
実施例5
オリーブ油の配合量を表−6の如く変化し、かつポリグ
リセリン側鎖脂肪酸エステルとしてジグリセリンジイノ
ステアレートを用いる他は、実施例1と同様にしてペー
スト状美白化粧科を調製した。Example 5 A whitening cosmetic paste was prepared in the same manner as in Example 1, except that the amount of olive oil was changed as shown in Table 6, and diglycerin diinostearate was used as the polyglycerin side chain fatty acid ester. .
表−6から明らかな如く、本発明の液状油の配合iiは
4〜50重量%である。4重景%よりも少なくな冫・と
べたつき感が増【7て好ましくない。50Mi.’56
よシも多くなるとアスコルビン酸高級脂肪k2f−=、
テルの結晶が析出しやナくなυ、冗沢に劣ろう
実施例6
オリーブ油(jil状油)の代りにノミ−7に示す液状
油を夫々に使用し、かつポリグリセリン魁]鎖脂肪酸エ
ステルとしてジグリ七リンジイソステアレートを用因る
他は、実施例1と同様にしてペースト状美白化粧料を調
興した。表−7の結果から明らかな如く本発明において
液状油として通常、常温下で液状を呈する油性物質を使
用すれば感触、光沢に優れ、色調等の経時変化(7)少
なイヘースト状美山化粧料が得られる。As is clear from Table 6, the liquid oil formulation ii of the present invention is 4 to 50% by weight. The feeling of stickiness has increased, which is less than the 4-layered view% [7], which is not desirable. 50 Mi. '56
When there is a lot of fat, ascorbic acid high-grade fat k2f-=,
Example 6 The liquid oil shown in No. 7 was used instead of olive oil (jelly oil), and polyglycerin chain fatty acid ester was used instead of olive oil (jelly oil). A paste-like whitening cosmetic was prepared in the same manner as in Example 1, except that Digly7rin diisostearate was used as the base material. As is clear from the results in Table 7, if an oily substance that is normally liquid at room temperature is used as the liquid oil in the present invention, an Iheaste-like Miyama cosmetic with excellent feel and gloss and little change in color tone over time (7) can be obtained. can get.
−59-59
Claims (1)
のアスコルビン酸高級脂肪酸エステルと液状のポリグリ
セリン側鎖高級脂肪酸エステルと、液状油とからなるこ
とを特徴とするペースト状の美白化粧料。 (2)アスコルピン酸高級脂肪酸エステルが、アスコル
ビン酸モノステアレートアスコルピン酸モノパルミテー
ト、アスコルビン酸モノオレート、アスコルビン酸ジパ
ルミテート、アスコルビン酸ジオレート、アスコルビン
酸ジステアレート、アスコルピン酸トリノ《ノレミテー
トあるいはそれらの組合せである、特許請求の範囲第(
1)項記載の美白化粧料0(3)アスコルビン酸高級脂
肪酸エステルが、処,+全量重短に対して8〜20重量
%配合されている特許詞求の範囲第(1)項記載の美白
化粧料。 (4)液状のポリグリセリン側鎖高級脂肪酸エステルが
、部分エステルであシ、かつ未反応OH基が1分子当シ
平均2個以上残存したものである、特許請求の範囲第(
1)項記載の美白化粧料。 (5)液状のポリグリセリン側鎖高級脂肪酸エステルカ
;、下記の式 (式中で、Rは水素原子または炭素数8以上の側鎖高級
脂肪酸残基である。ただし、Rは1分子当92個以上水
素原子であるが、全部が水素原子であることはない。n
はOまたは1〜8である。) で表わされる化合物の少なく一つである、特許請求の範
囲記載の美白化粧料。 (3)液状のポリグリセリン側鎖高級脂肪酸エステルが
、処4寄全量重量に対して40〜90重量%配合されて
いる特許請求の範囲第(1)項記載の美白化粧料。 (4)液状油が、アーモンド油、オリーブ油、ゴマ油、
サフラワー油、ミンク油、アボカド油、ホホバ油、イソ
グロビルミリステート、イソプロビルlクルミテート、
オクチルドテンルミリステート、イソプロビルインステ
アレート、デシルオレート、ヘキシルラウレート、シイ
ソブ口ピルアジペート、ジイソプロビルセバケート、オ
レイルアルコール、インステアリルアルコール、オクテ
ルトテヵノール、ヘキシルドデカノール、ヘキシルデヵ
ノールへプチルウンデカノールあるいはそれらの組合せ
である、特許請求の範囲第(1)項記載の美白化粧料。 (5)液状油が、処a全ロ量に対して4〜50重量%配
合されている特許請求の範囲第(1)項記載の美白化粧
料。[Claims] (1) 6 to 40 weight percent (based on the total weight of prescription ingredients)
1. A paste-like whitening cosmetic comprising a higher fatty acid ester of ascorbic acid, a liquid polyglycerin side chain higher fatty acid ester, and a liquid oil. (2) the ascorbic acid higher fatty acid ester is ascorbic acid monostearate, ascorbic acid monopalmitate, ascorbic acid monooleate, ascorbic acid dipalmitate, ascorbic acid dioleate, ascorbic acid distearate, ascorbic acid torino<<noremitate>, or a combination thereof; Claim No. (
Whitening cosmetics described in paragraph 1) (3) Ascorbic acid higher fatty acid ester is blended in an amount of 8 to 20% by weight based on the total weight and shortness of the skin whitening cosmetic according to paragraph (1). Cosmetics. (4) The liquid polyglycerin side-chain higher fatty acid ester is a partial ester and has an average of two or more unreacted OH groups remaining per molecule.
Whitening cosmetics described in section 1). (5) Liquid polyglycerin side chain higher fatty acid ester; the following formula (in the formula, R is a hydrogen atom or a side chain higher fatty acid residue having 8 or more carbon atoms. However, R is 92 per molecule) The above are hydrogen atoms, but not all of them are hydrogen atoms.n
is O or 1-8. ) A whitening cosmetic according to the claims, which is at least one of the compounds represented by: (3) The whitening cosmetic according to claim (1), wherein the liquid polyglycerin side chain higher fatty acid ester is blended in an amount of 40 to 90% by weight based on the total weight of the liquid. (4) The liquid oil is almond oil, olive oil, sesame oil,
Safflower oil, mink oil, avocado oil, jojoba oil, isoglobil myristate, isoprovir l curmitate,
Octyldothenelumiristate, isoprobyl instearate, decyl oleate, hexyl laurate, diisobutyradipate, diisoprobyl sebacate, oleyl alcohol, instearyl alcohol, octertotecanol, hexyldodecanol, hexyldecanol The whitening cosmetic according to claim (1), which is putylundecanol or a combination thereof. (5) The whitening cosmetic according to claim (1), wherein the liquid oil is blended in an amount of 4 to 50% by weight based on the total amount of treatment a.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP57215339A JPS59104308A (en) | 1982-12-06 | 1982-12-06 | Pasty cosmetic for whitening skin color |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP57215339A JPS59104308A (en) | 1982-12-06 | 1982-12-06 | Pasty cosmetic for whitening skin color |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS59104308A true JPS59104308A (en) | 1984-06-16 |
| JPH0330567B2 JPH0330567B2 (en) | 1991-04-30 |
Family
ID=16670656
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP57215339A Granted JPS59104308A (en) | 1982-12-06 | 1982-12-06 | Pasty cosmetic for whitening skin color |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS59104308A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS61207316A (en) * | 1985-03-13 | 1986-09-13 | Shiseido Co Ltd | External agent for skin |
-
1982
- 1982-12-06 JP JP57215339A patent/JPS59104308A/en active Granted
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS61207316A (en) * | 1985-03-13 | 1986-09-13 | Shiseido Co Ltd | External agent for skin |
Also Published As
| Publication number | Publication date |
|---|---|
| JPH0330567B2 (en) | 1991-04-30 |
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