JP4450427B2 - 皮膚化粧料 - Google Patents
皮膚化粧料 Download PDFInfo
- Publication number
- JP4450427B2 JP4450427B2 JP2007294276A JP2007294276A JP4450427B2 JP 4450427 B2 JP4450427 B2 JP 4450427B2 JP 2007294276 A JP2007294276 A JP 2007294276A JP 2007294276 A JP2007294276 A JP 2007294276A JP 4450427 B2 JP4450427 B2 JP 4450427B2
- Authority
- JP
- Japan
- Prior art keywords
- component
- urethane resin
- acid
- oil
- mass
- 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 - Fee Related
Links
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- LRBQNJMCXXYXIU-NRMVVENXSA-N tannic acid Chemical compound OC1=C(O)C(O)=CC(C(=O)OC=2C(=C(O)C=C(C=2)C(=O)OC[C@@H]2[C@H]([C@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)[C@@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)[C@@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)O2)OC(=O)C=2C=C(OC(=O)C=3C=C(O)C(O)=C(O)C=3)C(O)=C(O)C=2)O)=C1 LRBQNJMCXXYXIU-NRMVVENXSA-N 0.000 description 1
- 229920002258 tannic acid Polymers 0.000 description 1
- 235000015523 tannic acid Nutrition 0.000 description 1
- 229940033123 tannic acid Drugs 0.000 description 1
- 229940104261 taurate Drugs 0.000 description 1
- TUNFSRHWOTWDNC-HKGQFRNVSA-N tetradecanoic acid Chemical compound CCCCCCCCCCCCC[14C](O)=O TUNFSRHWOTWDNC-HKGQFRNVSA-N 0.000 description 1
- BORJONZPSTVSFP-UHFFFAOYSA-N tetradecyl 2-hydroxypropanoate Chemical compound CCCCCCCCCCCCCCOC(=O)C(C)O BORJONZPSTVSFP-UHFFFAOYSA-N 0.000 description 1
- DZKXJUASMGQEMA-UHFFFAOYSA-N tetradecyl tetradecanoate Chemical compound CCCCCCCCCCCCCCOC(=O)CCCCCCCCCCCCC DZKXJUASMGQEMA-UHFFFAOYSA-N 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- BSYVTEYKTMYBMK-UHFFFAOYSA-N tetrahydrofurfuryl alcohol Chemical compound OCC1CCCO1 BSYVTEYKTMYBMK-UHFFFAOYSA-N 0.000 description 1
- KWXLCDNSEHTOCB-UHFFFAOYSA-J tetrasodium;1,1-diphosphonatoethanol Chemical compound [Na+].[Na+].[Na+].[Na+].[O-]P(=O)([O-])C(O)(C)P([O-])([O-])=O KWXLCDNSEHTOCB-UHFFFAOYSA-J 0.000 description 1
- UEUXEKPTXMALOB-UHFFFAOYSA-J tetrasodium;2-[2-[bis(carboxylatomethyl)amino]ethyl-(carboxylatomethyl)amino]acetate Chemical compound [Na+].[Na+].[Na+].[Na+].[O-]C(=O)CN(CC([O-])=O)CCN(CC([O-])=O)CC([O-])=O UEUXEKPTXMALOB-UHFFFAOYSA-J 0.000 description 1
- OULAJFUGPPVRBK-UHFFFAOYSA-N tetratriacontyl alcohol Natural products CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCO OULAJFUGPPVRBK-UHFFFAOYSA-N 0.000 description 1
- SHWIJIJNPFXOFS-UHFFFAOYSA-N thiotaurine Chemical compound NCCS(O)(=O)=S SHWIJIJNPFXOFS-UHFFFAOYSA-N 0.000 description 1
- 229940098465 tincture Drugs 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- 229930003799 tocopherol Natural products 0.000 description 1
- 239000011732 tocopherol Substances 0.000 description 1
- 125000002640 tocopherol group Chemical class 0.000 description 1
- 235000019149 tocopherols Nutrition 0.000 description 1
- 229950009883 tocopheryl nicotinate Drugs 0.000 description 1
- DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 description 1
- 230000000699 topical effect Effects 0.000 description 1
- GYDJEQRTZSCIOI-LJGSYFOKSA-N tranexamic acid Chemical compound NC[C@H]1CC[C@H](C(O)=O)CC1 GYDJEQRTZSCIOI-LJGSYFOKSA-N 0.000 description 1
- 229960000401 tranexamic acid Drugs 0.000 description 1
- ILJSQTXMGCGYMG-UHFFFAOYSA-N triacetic acid Chemical compound CC(=O)CC(=O)CC(O)=O ILJSQTXMGCGYMG-UHFFFAOYSA-N 0.000 description 1
- QORWJWZARLRLPR-UHFFFAOYSA-H tricalcium bis(phosphate) Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O QORWJWZARLRLPR-UHFFFAOYSA-H 0.000 description 1
- 239000001069 triethyl citrate Substances 0.000 description 1
- VMYFZRTXGLUXMZ-UHFFFAOYSA-N triethyl citrate Natural products CCOC(=O)C(O)(C(=O)OCC)C(=O)OCC VMYFZRTXGLUXMZ-UHFFFAOYSA-N 0.000 description 1
- 235000013769 triethyl citrate Nutrition 0.000 description 1
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1
- JLGLQAWTXXGVEM-UHFFFAOYSA-N triethylene glycol monomethyl ether Chemical compound COCCOCCOCCO JLGLQAWTXXGVEM-UHFFFAOYSA-N 0.000 description 1
- 229940118594 trimethylolpropane triisostearate Drugs 0.000 description 1
- 150000004072 triols Chemical class 0.000 description 1
- 229960005066 trisodium edetate Drugs 0.000 description 1
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 description 1
- UJMBCXLDXJUMFB-UHFFFAOYSA-K trisodium;5-oxo-1-(4-sulfonatophenyl)-4-[(4-sulfonatophenyl)diazenyl]-4h-pyrazole-3-carboxylate Chemical compound [Na+].[Na+].[Na+].[O-]C(=O)C1=NN(C=2C=CC(=CC=2)S([O-])(=O)=O)C(=O)C1N=NC1=CC=C(S([O-])(=O)=O)C=C1 UJMBCXLDXJUMFB-UHFFFAOYSA-K 0.000 description 1
- SOBHUZYZLFQYFK-UHFFFAOYSA-K trisodium;hydroxy-[[phosphonatomethyl(phosphonomethyl)amino]methyl]phosphinate Chemical compound [Na+].[Na+].[Na+].OP(O)(=O)CN(CP(O)([O-])=O)CP([O-])([O-])=O SOBHUZYZLFQYFK-UHFFFAOYSA-K 0.000 description 1
- PBYZMCDFOULPGH-UHFFFAOYSA-N tungstate Chemical compound [O-][W]([O-])(=O)=O PBYZMCDFOULPGH-UHFFFAOYSA-N 0.000 description 1
- 239000006097 ultraviolet radiation absorber Substances 0.000 description 1
- LNRUEZIDUKQGRH-YZUCMPLFSA-N umbelliferose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O[C@@H]2[C@@H]([C@@H](O)[C@@H](O)[C@@H](CO)O2)O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 LNRUEZIDUKQGRH-YZUCMPLFSA-N 0.000 description 1
- 229960002703 undecylenic acid Drugs 0.000 description 1
- 229960001722 verapamil Drugs 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 235000019155 vitamin A Nutrition 0.000 description 1
- 239000011719 vitamin A Substances 0.000 description 1
- 235000010374 vitamin B1 Nutrition 0.000 description 1
- 239000011691 vitamin B1 Substances 0.000 description 1
- 235000019164 vitamin B2 Nutrition 0.000 description 1
- 239000011716 vitamin B2 Substances 0.000 description 1
- 235000019158 vitamin B6 Nutrition 0.000 description 1
- 239000011726 vitamin B6 Substances 0.000 description 1
- 235000019154 vitamin C Nutrition 0.000 description 1
- 239000011718 vitamin C Substances 0.000 description 1
- 235000019165 vitamin E Nutrition 0.000 description 1
- 239000011709 vitamin E Substances 0.000 description 1
- 239000010497 wheat germ oil Substances 0.000 description 1
- 239000012463 white pigment Substances 0.000 description 1
- 239000001052 yellow pigment Substances 0.000 description 1
- 239000009538 yokuinin Substances 0.000 description 1
- 239000010457 zeolite Substances 0.000 description 1
- 229940105125 zinc myristate Drugs 0.000 description 1
- GBFLQPIIIRJQLU-UHFFFAOYSA-L zinc;tetradecanoate Chemical compound [Zn+2].CCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCC([O-])=O GBFLQPIIIRJQLU-UHFFFAOYSA-L 0.000 description 1
- OJYLAHXKWMRDGS-UHFFFAOYSA-N zingerone Chemical compound COC1=CC(CCC(C)=O)=CC=C1O OJYLAHXKWMRDGS-UHFFFAOYSA-N 0.000 description 1
- 229910052726 zirconium Inorganic materials 0.000 description 1
- 239000004711 α-olefin Substances 0.000 description 1
- FYGDTMLNYKFZSV-BYLHFPJWSA-N β-1,4-galactotrioside Chemical compound O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@H]1O[C@@H]1[C@H](CO)O[C@@H](O[C@@H]2[C@@H](O[C@@H](O)[C@H](O)[C@H]2O)CO)[C@H](O)[C@H]1O FYGDTMLNYKFZSV-BYLHFPJWSA-N 0.000 description 1
- OENHQHLEOONYIE-JLTXGRSLSA-N β-Carotene Chemical compound CC=1CCCC(C)(C)C=1\C=C\C(\C)=C\C=C\C(\C)=C\C=C\C=C(/C)\C=C\C=C(/C)\C=C\C1=C(C)CCCC1(C)C OENHQHLEOONYIE-JLTXGRSLSA-N 0.000 description 1
- 229930007845 β-thujaplicin Natural products 0.000 description 1
Classifications
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- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/84—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions otherwise than those involving only carbon-carbon unsaturated bonds
- A61K8/87—Polyurethanes
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- A61Q19/08—Anti-ageing preparations
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/08—Processes
- C08G18/0804—Manufacture of polymers containing ionic or ionogenic groups
- C08G18/0819—Manufacture of polymers containing ionic or ionogenic groups containing anionic or anionogenic groups
- C08G18/0823—Manufacture of polymers containing ionic or ionogenic groups containing anionic or anionogenic groups containing carboxylate salt groups or groups forming them
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/08—Processes
- C08G18/10—Prepolymer processes involving reaction of isocyanates or isothiocyanates with compounds having active hydrogen in a first reaction step
- C08G18/12—Prepolymer processes involving reaction of isocyanates or isothiocyanates with compounds having active hydrogen in a first reaction step using two or more compounds having active hydrogen in the first polymerisation step
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/2805—Compounds having only one group containing active hydrogen
- C08G18/285—Nitrogen containing compounds
- C08G18/2865—Compounds having only one primary or secondary amino group; Ammonia
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/30—Low-molecular-weight compounds
- C08G18/32—Polyhydroxy compounds; Polyamines; Hydroxyamines
- C08G18/3203—Polyhydroxy compounds
- C08G18/3212—Polyhydroxy compounds containing cycloaliphatic groups
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
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- C08G18/30—Low-molecular-weight compounds
- C08G18/32—Polyhydroxy compounds; Polyamines; Hydroxyamines
- C08G18/3271—Hydroxyamines
- C08G18/3275—Hydroxyamines containing two hydroxy groups
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/40—High-molecular-weight compounds
- C08G18/48—Polyethers
- C08G18/4804—Two or more polyethers of different physical or chemical nature
- C08G18/4808—Mixtures of two or more polyetherdiols
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/40—High-molecular-weight compounds
- C08G18/48—Polyethers
- C08G18/4833—Polyethers containing oxyethylene units
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/40—High-molecular-weight compounds
- C08G18/61—Polysiloxanes
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/65—Low-molecular-weight compounds having active hydrogen with high-molecular-weight compounds having active hydrogen
- C08G18/66—Compounds of groups C08G18/42, C08G18/48, or C08G18/52
- C08G18/6666—Compounds of group C08G18/48 or C08G18/52
- C08G18/6692—Compounds of group C08G18/48 or C08G18/52 with compounds of group C08G18/34
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
- C08G18/72—Polyisocyanates or polyisothiocyanates
- C08G18/74—Polyisocyanates or polyisothiocyanates cyclic
- C08G18/75—Polyisocyanates or polyisothiocyanates cyclic cycloaliphatic
- C08G18/751—Polyisocyanates or polyisothiocyanates cyclic cycloaliphatic containing only one cycloaliphatic ring
- C08G18/752—Polyisocyanates or polyisothiocyanates cyclic cycloaliphatic containing only one cycloaliphatic ring containing at least one isocyanate or isothiocyanate group linked to the cycloaliphatic ring by means of an aliphatic group
- C08G18/753—Polyisocyanates or polyisothiocyanates cyclic cycloaliphatic containing only one cycloaliphatic ring containing at least one isocyanate or isothiocyanate group linked to the cycloaliphatic ring by means of an aliphatic group containing one isocyanate or isothiocyanate group linked to the cycloaliphatic ring by means of an aliphatic group having a primary carbon atom next to the isocyanate or isothiocyanate group
- C08G18/755—Polyisocyanates or polyisothiocyanates cyclic cycloaliphatic containing only one cycloaliphatic ring containing at least one isocyanate or isothiocyanate group linked to the cycloaliphatic ring by means of an aliphatic group containing one isocyanate or isothiocyanate group linked to the cycloaliphatic ring by means of an aliphatic group having a primary carbon atom next to the isocyanate or isothiocyanate group and at least one isocyanate or isothiocyanate group linked to a secondary carbon atom of the cycloaliphatic ring, e.g. isophorone diisocyanate
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
- A61K2800/40—Chemical, physico-chemical or functional or structural properties of particular ingredients
- A61K2800/54—Polymers characterized by specific structures/properties
- A61K2800/542—Polymers characterized by specific structures/properties characterized by the charge
- A61K2800/5424—Polymers characterized by specific structures/properties characterized by the charge anionic
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
- A61K2800/40—Chemical, physico-chemical or functional or structural properties of particular ingredients
- A61K2800/54—Polymers characterized by specific structures/properties
- A61K2800/542—Polymers characterized by specific structures/properties characterized by the charge
- A61K2800/5428—Polymers characterized by specific structures/properties characterized by the charge amphoteric or zwitterionic
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Dermatology (AREA)
- Epidemiology (AREA)
- Birds (AREA)
- Gerontology & Geriatric Medicine (AREA)
- Engineering & Computer Science (AREA)
- Manufacturing & Machinery (AREA)
- Cosmetics (AREA)
- Polyurethanes Or Polyureas (AREA)
Description
(b−1)成分:シクロヘキサンジメタノール
(b−2)成分:分子量1000〜3000のポリプロピレングリコール
(b−3)成分:一分子中に活性水素とカルボキシル基を有する化合物
(b−1)成分:シクロヘキサンジメタノール
(b−2)成分:分子量1000〜3000のポリプロピレングリコール
(b−3)成分:一分子中に活性水素とカルボキシル基を有する化合物
(b−4)成分:一分子中に活性水素と第三級アミノ基を有する化合物
(製造例1)
攪拌装置、温度計、窒素導入管および還流冷却器を備えたガラス製4つのフラスコに、イソホロンジイソシアネート(IPDI)100g、ポリプロピレングリコール(PPG1000)66g、1,4−シクロヘキサンジメタノール(CHDM)10gおよびジメチロールブタン酸(DMBA)38gを入れ、溶剤として酢酸エチル60gを加え、オイルバスで80℃に加熱して4時間反応させ、NCO基の残存したポリウレタンプレポリマーの溶液を得た。このNCO基の残存したポリウレタンポリマーを、水酸化カリウム16gを含む水750g中に分散させ、50℃にて3時間鎖延長反応を行って、高分子量化させた。得られた水分散液から酢酸エチルを減圧下回収し、実質的に溶剤を含まないアニオン性ウレタン樹脂の25質量%水分散液を得た。
CHDM/PPG1000=約0.15(質量比。仕込み量)。
攪拌装置、温度計、窒素導入管および還流冷却器を備えたガラス製4つ口フラスコに、イソホロンジイソシアネート(IPDI)100g、ポリプロピレングリコール(PPG1000)66g、シクロヘキサンジメタノール(CHDM)100g、ポリオキシエチレングリコール(PEG1000)20gおよびジメチロールブタン酸(DMBA)36gを入れ、溶剤として酢酸エチル60gを加え、オイルバスで80℃に加熱して4時間反応させた。その後、N−メチルジエタノールアミン2gおよび酢酸エチル30gを追加して添加し、さらに3時間反応させた。これにさらに、片末端に1つのアミノ基を有するポリプロピレングリコール(「ジェファーミンM1000」;HUNTSMAN社製)30gおよび酢酸エチル50gを加え、さらに1時間反応させて、NCO基の残存したポリウレタンプレポリマーの溶液を得た。このNCO基の残存したポリウレタンポリマーを、水酸化カリウム15gを含む水750g中に分散させ、50℃にて3時間鎖延長反応を行って高分子量化させた。得られた水分散液から酢酸エチルを減圧下回収し、実質的に溶剤を含まず、エチレンオキシド鎖を構造中に有する両性ウレタン樹脂の30質量%水分散液を得た。
CHDM/PPG1000=約1.5(質量比。仕込み量)。
攪拌装置、温度計、窒素導入管および還流冷却器を備えたガラス製4つのフラスコに、イソホロンジイソシアネート(IPDI)100g、ポリプロピレングリコール(PPG1000)60g、1,4−シクロヘキサンジメタノール(CHDM)30gおよびジメチロールブタン酸(DMBA)38gを入れ、溶剤として酢酸エチル60gを加え、オイルバスで80℃に加熱して4時間反応させ、NCO基の残存したポリウレタンプレポリマーの溶液を得た。このNCO基の残存したポリウレタンポリマーを、水酸化カリウム16gを含む水750g中に分散させ、50℃にて3時間鎖延長反応を行って、高分子量化させた。得られた水分散液から酢酸エチルを減圧下回収し、実質的に溶剤を含まないアニオン性ウレタン樹脂の26質量%水分散液を得た。
CHDM/PPG1000=0.5(質量比。仕込み量)。
攪拌装置、温度計、窒素導入管および還流冷却器を備えたガラス製4つ口フラスコに、イソホロンジイソシアネート(IPDI)100gおよび片末端にOH基を2つ有するポリジメチルシロキサンジオール(分子量1000)3gを入れ、オイルバスで80℃に加熱して2時間反応させた。その後、ポリプロピレングリコール(PPG3000)20g、1,4−シクロヘキサンジメタノール(CHDM)60g、水素添加ビスフェノールA5gおよびジメチロールブタン酸(DMBA)36gを入れ、溶剤として酢酸エチル60gを加え、オイルバスで80℃に加熱して4時間反応させた。その後、N−メチルジエタノールアミン2gおよび酢酸エチル30gを追加して添加し、さらに3時間反応させた。これにさらに、片末端に1つのアミノ基を有するポリプロピレングリコール(「ジェファーミンM1000」;HUNTSMAN社製)30gおよび酢酸エチル50gを加え、さらに1時間反応させて、NCO基の残存したポリウレタンプレポリマーの溶液を得た。このNCO基の残存したポリウレタンプレポリマーを、水酸化カリウム15gを含む水750g中に分散させ、50℃にて3時間鎖延長反応を行って高分子量化させた。得られた水分散液から酢酸エチルを減圧下回収し、実質的に溶剤を含まず、ジメチルシロキサン鎖を構造中に有する両性ウレタン樹脂の27質量%水分散液を得た。
CHDM/PPG1000=3.0(質量比。仕込み量)。
攪拌装置、温度計、窒素導入管および還流冷却器を備えたガラス製4つのフラスコに、イソホロンジイソシアネート(IPDI)100g、ポリプロピレングリコール(PPG1000)60g、1,4−シクロヘキサンジメタノール(CHDM)5gおよびジメチロールブタン酸(DMBA)38gを入れ、溶剤として酢酸エチル60gを加え、オイルバスで80℃に加熱して4時間反応させた。その後、N−メチルジエタノールアミン2gならびに酢酸エチル30gを追加して添加し、さらに3時間反応させた。これにさらに、片末端に1つのアミノ基を有するポリプロピレングリコール(「ジェファーミンM1000」;HUNTSMAN社製)30gおよび酢酸エチル50gを加え、さらに1時間反応させて、NCO基の残存したポリウレタンプレポリマーの溶液を得た。このNCO基の残存したポリウレタンポリマーを、水酸化カリウム16gを含む水750g中に分散させ、50℃にて3時間鎖延長反応を行って、高分子量化させた。得られた水分散液から酢酸エチルを減圧下回収し、実質的に溶剤を含まない両性ウレタン樹脂の24質量%水分散液を得た。
CHDM/PPG1000=約0.08(質量比。仕込み量)。
攪拌装置、温度計、窒素導入管および還流冷却器を備えたガラス製4つ口フラスコに、イソホロンジイソシアネート(IPDI)100g、ポリプロピレングリコール(PPG1000)10g、1,4−シクロヘキサンジメタノール(CHDM)50g、ポリオキシエチレングリコール(PEG1000)20gおよびジメチロールブタン酸(DMBA)36gを入れ、溶剤として酢酸エチル60gを加え、オイルバスで80℃に加熱して4時間反応させた。その後、N−メチルジエタノールアミン2gおよび酢酸エチル30gを追加して添加し、さらに3時間反応させた。これにさらに、片末端に1つのアミノ基を有するポリプロピレングリコール(「ジェファーミンM1000」;HUNTSMAN社製)30gおよび酢酸エチル50gを加え、さらに1時間反応させて、NCO基の残存したポリウレタンプレポリマーの溶液を得た。このNCO基の残存したポリウレタンポリマーを、水酸化カリウム15gを含む水750g中に分散させ、50℃にて3時間鎖延長反応を行って高分子量化させた。得られた水分散液から酢酸エチルを減圧下回収し、実質的に溶剤を含まず、エチレンオキシド鎖を構造中に有する両性ウレタン樹脂の25%質量水分散液を得た。
CHDM/PPG1000=5.0(質量比。仕込み量)。
攪拌装置、温度計、窒素導入管および還流冷却器を備えたガラス製4つ口フラスコに、イソホロンジイソシアネート(IPDI)100gおよび片末端にOH基を2つ有するポリジメチルシロキサンジオール(分子量1000)3gを入れ、オイルバスで80℃に加熱して2時間反応させた。その後、ポリプロピレングリコール(PPG1000)10g、1,4−シクロヘキサンジメタノール(CHDM)40gおよびジメチロールブタン酸(DMBA)36gを入れ、溶剤として酢酸エチル60gを加え、オイルバスで80℃に加熱して4時間反応させた。その後、N−メチルジエタノールアミン2gならびに酢酸エチル30gを追加して添加し、さらに3時間反応させた。これにさらに、片末端に1つのアミノ基を有するポリプロピレングリコール(「ジェファーミンM1000」;HUNTSMAN社製)30gおよび酢酸エチル50gを加え、さらに1時間反応させて、NCO基の残存したポリウレタンプレポリマーの溶液を得た。このNCO基の残存したポリウレタンプレポリマーを、水酸化カリウム15gを含む水750g中に分散させ、50℃にて3時間鎖延長反応を行って高分子量化させた。得られた水分散液から酢酸エチルを減圧下回収し、実質的に溶剤を含まず、ジメチルシロキサン鎖を構造中に有する両性ウレタン樹脂の24質量%水分散液を得た。
CHDM/PPG1000=4.0(質量比。仕込み量)。
上記製造例1〜4、比較製造例1〜3で得たウレタン樹脂水分散液を用いて、表1〜2に示す皮膚化粧料(アイクリーム)を下記の方法で調製した。
(調製法)
表1〜2において、(1)に(2)〜(6)、(18)、(19)を加え、70℃に加温して、均一に溶解した(水相)。次いで、別釜に(7)〜(17)を80℃で均一に溶解した(油相)。70℃の水相をホモミキサーで撹拌した。これに80℃の油相を徐添しながら乳化し、最後に(20)〜(28)を添加して均一に撹拌してから冷却装置(オンレーター)により40℃以下まで急冷し、水中油型の皮膚化粧料(アイクリーム)を得た。
女性専門パネル(10名)により実際に皮膚に塗布して使用してもらい、「べたついた使用感の有無」、「きしみ感の有無」、「皮膚上でのよれの有無」および「しわ、たるみ(皮膚の張り)への効果感の有無」について、下記の評価区分に基づいて評価してもらった。
(評価区分)
非常にべたつきが少ない
べたつきが少ない
ややべたつく
べたつく
(評価基準)
◎:評価区分で「べたつきが少ない」以上の評価をした人が9名以上
○:評価区分で「べたつきが少ない」以上の評価をした人が6〜8名
△:評価区分で「べたつきが少ない」以上の評価をした人が3〜5名
×:評価区分で「べたつきが少ない」以上の評価をした人が2人以下。
(評価区分)
きしまない
きしみが感じられる
きしむ
(評価基準)
○:評価区分で「きしまない」と評価した人が9名以上
△:評価区分で「きしまない」と評価した人が2〜8名
×:評価区分で「きしまない」と評価した人が1名以下。
(評価区分)
よれがない
よれが感じられる
よれがある。
(評価基準)
○:評価区分で「よれがない」と評価した人が9名以上
△:評価区分で「よれがない」と評価した人が2〜8名
×:評価区分で「よれがない」と評価した人が1名以下。
(評価区分)
非常にしわ、たるみへの効果感がある
しわ、たるみへの効果感がある
ややしわ、たるみへの効果感がある
しわ、たるみへの効果感がない
(評価基準)
◎:評価区分で「しわ、たるみへの効果感がある」以上の評価をした人が9名以上
○:評価区分で「しわ、たるみへの効果感がある」以上の評価をした人が6〜8名
△:評価区分で「しわ、たるみへの効果感がある」以上の評価をした人が3〜5名
×:評価区分で「しわ、たるみへの効果感がある」以上の評価をした人が2名以下。
(配 合 成 分) (質量%)
(1)精製水 残余
(2)グリセリン 3.0
(3)1,3−ブチレングリコール 3.0
(4)エタノール 5.0
(5)POE(60モル付加)硬化ヒマシ油 0.3
(6)製造例1で得たアニオン性ウレタン樹脂水分散液 2.0(有効分0.5)
(7)フェノキシエタノール 0.5
(8)スギナエキス 0.1
(9)チョウジエキス 0.1
(10)クレマティスエキス 0.1
(11)アルテア根エキス 0.1
(12)メリッサエキス 0.1
(13)オウゴンエキス 0.1
(14)ビニルピロリドン/AMPS共重合体 0.05
(15)ジメチルポリシロキサン(5mPa・s) 0.01
(16)香料 0.1
(製法)
(4)、(5)の混合物に(15)、(16)を加え、これを(1)に添加して可溶化を行った(主水相)。次いで、先の主水相に(2)、(3)、(7)〜(14)を添加して、最後に(6)を添加して目的の可溶化型化粧水を得た。
(配 合 成 分) (質量%)
(1)精製水 残余
(2)カルボキシビニルポリマー 0.3
(3)エタノール 3.0
(4)グリセリン 1.0
(5)ジプロピレングリコール 5.0
(6)製造例1で得たアニオン性ウレタン樹脂水分散液 4.0(有効分1.0)
(7)ステアリルアルコール 3.0
(8)セチルアルコール 5.0
(9)モノヤシ油脂肪酸POE(20)ソルビタン 1.0
(10)POE(20)硬化ヒマシ油 0.5
(11)水酸化ナトリウム 0.1
(12)アセンヤクエキス 0.01
(13)L−アルギニン 0.01
(14)ブナノメエキス 0.01
(15)ウコンエキス 0.01
(16)パラベン 0.1
(17)香料 0.1
(18)流動パラフィン 3.0
(19)ジメチルシリコーン(6mPa・s) 3.0
(製法)
(1)に(2)〜(5)および(11)〜(15)を加え、均一に溶解した(水相)。次いで、別釜にて(7)〜(10)および(16)〜(19)を80℃にて均一に混合溶解した(油相)。70℃に加温した水相をホモミキサーで撹拌し、これに80℃の油相を徐添し乳化した。乳化終了後、(6)を添加して、均一に攪拌した。次いで、脱気、濾過をして目的の水中油型乳化型クリームを得た。
(配 合 成 分) (質量%)
(1)精製水 残余
(2)ポリアクリル酸ナトリウム/AMPS共重合体 1.0
(3)1,3−ブチレングリコール 5.0
(4)製造例2で得た両性ウレタン樹脂水分散液 5.0(有効分1.5)
(5)ワセリン 1.0
(6)オクタン酸セチル 1.0
(7)トリオクタノイン 0.1
(8)ベヘニルアルコール 2.0
(9)ステアリルアルコール 2.0
(10)アラキルアルコール 1.0
(11)POE(20)ベヘニルアルコール 3.0
(12)セトステアリルグルコシド 0.1
(13)グリチルリチン酸ジカリウム 0.05
(14)ビタミンEアセテート 0.1
(15)大豆エキス 0.01
(16)パラベン 0.15
(17)香料 0.1
(製法)
(1)に(2)(3)および(13)〜(15)を加え、均一に溶解した(水相)。次いで、別釜にて(5)〜(12)および(16)、(17)を70℃にて均一に混合溶解した(油相)。70℃に加温した水相をホモミキサーで撹拌し、これに70℃の油相を徐添し乳化した。乳化終了後、(4)を添加して、均一に攪拌した。次いで、脱気、濾過をして目的の水中油型乳化型乳液を得た。
(配 合 成 分) (質量%)
(1)精製水 残余
(2)ポリアクリル酸ナトリウム 1.5
(3)エタノール 3.0
(4)グリセリン 1.0
(5)ジプロピレングリコール 5.0
(6)製造例3で得たアニオン性ウレタン樹脂水分散液 0.38(有効分0.1)
(7)ステアリルアルコール 1.0
(8)セチルアルコール 1.0
(9)モノヤシ油脂肪酸POE(20)ソルビタン 0.3
(10)POE(20)硬化ヒマシ油 0.2
(11)水酸化ナトリウム 0.1
(12)アセンヤクエキス 0.01
(13)L−アルギニン 0.01
(14)ブナノメエキス 0.01
(15)ウコンエキス 0.01
(16)パラベン 0.1
(17)香料 0.1
(18)流動パラフィン 3.0
(19)ジメチルシリコーン(6mPa・s) 3.0
(製法)
(1)に(2)〜(5)および(11)〜(15)を加え、均一に溶解した(水相)。次いで、別釜にて(7)〜(10)および(16)〜(19)を70℃にて均一に混合溶解した(油相)。70℃に加温した水相をホモミキサーで撹拌し、これに70℃の油相を徐添し乳化した。乳化終了後、(6)を添加して、均一に攪拌した。次いで、脱気、濾過をして目的の水中油型乳化型クリームを得た。
(配 合 成 分) (質量%)
(1)精製水 残余
(2)アクリル酸/アクリル酸アルキル(C10-30)共重合体 0.3
(3)1,3−ブチレングリコール 5.0
(4)製造例4で得た両性ウレタン樹脂水分散液 11.1(有効分3.0)
(5)ワセリン 1.0
(6)オクタン酸セチル 1.0
(7)トリオクタノイン 0.1
(8)ベヘニルアルコール 1.0
(9)ステアリルアルコール 0.5
(10)アラキルアルコール 0.5
(11)POE(20)ベヘニルアルコール 0.5
(12)セトステアリルグルコシド 0.1
(13)グリチルリチン酸ジカリウム 0.05
(14)ビタミンEアセテート 0.1
(15)大豆エキス 0.01
(16)パラベン 0.15
(17)香料 0.1
(18)水酸化カリウム 0.1
(製法)
(1)に(2)、(3)および(13)〜(15)を加え、均一に溶解した(水相)。次いで、別釜にて(5)〜(12)および(16)、(17)を70℃にて均一に混合溶解した(油相)。70℃に加温した水相をホモミキサーで撹拌し、これに70℃の油相を徐添し乳化した。乳化終了後、(4)および(18)を添加して均一に撹拌した。次いで、脱気、濾過をして目的の水中油型乳化型美容液を得た。
Claims (6)
- (a)イソシアネート化合物と、(b)下記(b−1)〜(b−3)成分を含み、かつ(b−1)成分/(b−2)成分=0.15〜3.0(質量比。仕込み量)であるポリオール化合物とを反応させて製造したアニオン性ウレタン樹脂を水に溶解または分散してなるアニオン性ウレタン樹脂水性液を含有することを特徴とする皮膚化粧料。
(b−1)成分:シクロヘキサンジメタノール
(b−2)成分:分子量1000〜3000のポリプロピレングリコール
(b−3)成分:一分子中に活性水素とカルボキシル基を有する化合物 - 上記アニオン性ウレタン樹脂が、その構造中にエチレンオキシドから誘導される構造単位を有するものである、請求項1記載の皮膚化粧料。
- 皮膚化粧料中の上記アニオン性ウレタン樹脂水性液の配合量(実分。有効分)が0.1〜5質量%である、請求項1または2記載の皮膚化粧料。
- (a)イソシアネート化合物と、(b)下記(b−1)〜(b−4)成分を含み、かつ(b−1)成分/(b−2)成分=0.15〜3.0(質量比。仕込み量)であるポリオール化合物とを反応させて製造した両性ウレタン樹脂を水に溶解または分散してなる両性ウレタン樹脂水性液を含有することを特徴とする皮膚化粧料。
(b−1)成分:シクロヘキサンジメタノール
(b−2)成分:分子量1000〜3000のポリプロピレングリコール
(b−3)成分:一分子中に活性水素とカルボキシル基を有する化合物
(b−4)成分:一分子中に活性水素と第三級アミノ基を有する化合物 - 上記両性ウレタン樹脂が、その構造中にエチレンオキシドから誘導される構造単位を有するものである、請求項4記載の皮膚化粧料。
- 皮膚化粧料中の上記両性ウレタン樹脂水性液の配合量(実分。有効分)が0.1〜5質量%である、請求項4または5記載の皮膚化粧料。
Priority Applications (8)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2007294276A JP4450427B2 (ja) | 2007-11-13 | 2007-11-13 | 皮膚化粧料 |
| PCT/JP2008/070611 WO2009063917A1 (ja) | 2007-11-13 | 2008-11-12 | 皮膚化粧料 |
| CN2008801246410A CN101917964B (zh) | 2007-11-13 | 2008-11-12 | 皮肤化妆品 |
| KR1020107012987A KR20100101104A (ko) | 2007-11-13 | 2008-11-12 | 피부 화장료 |
| US12/742,444 US8642023B2 (en) | 2007-11-13 | 2008-11-12 | Skin cosmetic |
| HK11100738.4A HK1146580B (en) | 2007-11-13 | 2008-11-12 | Skin cosmetic |
| EP08848813.5A EP2221046A4 (en) | 2007-11-13 | 2008-11-12 | SKIN CARE PREPARATIONS |
| US14/150,098 US20140120051A1 (en) | 2007-11-13 | 2014-01-08 | Skin Cosmetic |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2007294276A JP4450427B2 (ja) | 2007-11-13 | 2007-11-13 | 皮膚化粧料 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2009120510A JP2009120510A (ja) | 2009-06-04 |
| JP4450427B2 true JP4450427B2 (ja) | 2010-04-14 |
Family
ID=40638766
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2007294276A Expired - Fee Related JP4450427B2 (ja) | 2007-11-13 | 2007-11-13 | 皮膚化粧料 |
Country Status (6)
| Country | Link |
|---|---|
| US (2) | US8642023B2 (ja) |
| EP (1) | EP2221046A4 (ja) |
| JP (1) | JP4450427B2 (ja) |
| KR (1) | KR20100101104A (ja) |
| CN (1) | CN101917964B (ja) |
| WO (1) | WO2009063917A1 (ja) |
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| RU2488378C2 (ru) * | 2008-12-03 | 2013-07-27 | Шисейдо Компани, Лтд. | Косметическое средство в форме масло-в-воде |
| US8106111B2 (en) | 2009-05-15 | 2012-01-31 | Eastman Chemical Company | Antimicrobial effect of cycloaliphatic diol antimicrobial agents in coating compositions |
| CN105664223B (zh) | 2009-10-26 | 2018-12-04 | 日产化学工业株式会社 | 化妆料、皮肤外用剂、以及医疗用仪器 |
| JP4837086B2 (ja) * | 2009-12-15 | 2011-12-14 | 株式会社 資生堂 | 乳化化粧料 |
| CN102294132B (zh) * | 2011-06-29 | 2013-09-25 | 南京四新科技应用研究所有限公司 | 一种印制电路板清洗用消泡剂 |
| CN103975017A (zh) * | 2011-12-09 | 2014-08-06 | Dic株式会社 | 成膜助剂、含有其的水性树脂组合物及钢板表面处理剂 |
| US9975981B2 (en) * | 2013-08-07 | 2018-05-22 | Japan Coating Resin Corporation | Polyurethane, urethane-(meth)acrylic composite resin, and aqueous dispersion of urethane-(meth)acrylic composite resin |
| JP6969352B2 (ja) * | 2017-12-20 | 2021-11-24 | 東洋インキScホールディングス株式会社 | 皮膚貼付用粘着剤、皮膚用貼付剤、および剥離用シート状部材付き皮膚用貼付剤の製造方法 |
| JP7343310B2 (ja) * | 2019-06-10 | 2023-09-12 | 株式会社Adeka | 皮膚化粧料 |
| JP2021143127A (ja) * | 2020-03-10 | 2021-09-24 | ロゼット株式会社 | ゴマージュ化粧料組成物 |
| CN112480365B (zh) * | 2020-11-26 | 2022-06-07 | 文水县是大高分子材料有限公司 | 一种聚氨酯分散剂及其制备方法和应用 |
Family Cites Families (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP3535322B2 (ja) | 1996-09-28 | 2004-06-07 | 株式会社資生堂 | 皮膚外用剤 |
| US5968494A (en) * | 1998-02-24 | 1999-10-19 | National Starch And Chemical Investment Holding Corporation | Polyurethanes with carboxylate functionality for hair fixative applications |
| JP2000063253A (ja) | 1998-08-19 | 2000-02-29 | Shiseido Co Ltd | しわ改善化粧方法及びこれに使用する化粧品 |
| WO2002005621A1 (en) * | 2000-04-13 | 2002-01-24 | National Starch And Chemical Investment Holding Corporation | Cosmetic resin composition and cosmetic using the same |
| JP2002020451A (ja) * | 2000-07-07 | 2002-01-23 | Nippon Nsc Ltd | 両性ウレタン樹脂組成物 |
| JP4688351B2 (ja) * | 2001-06-27 | 2011-05-25 | アクゾノーベル株式会社 | 両性ウレタン樹脂の製造方法、その製造方法で得られる両性ウレタン樹脂及び樹脂組成物 |
| JP2003012440A (ja) * | 2001-06-27 | 2003-01-15 | Shiseido Co Ltd | 化粧料 |
| JP3701233B2 (ja) * | 2001-12-04 | 2005-09-28 | 株式会社資生堂 | 毛髪化粧料 |
| JP3701232B2 (ja) * | 2001-12-04 | 2005-09-28 | 株式会社資生堂 | 毛髪化粧料 |
| JP3701234B2 (ja) * | 2001-12-04 | 2005-09-28 | 株式会社資生堂 | 毛髪化粧料 |
| JP3701238B2 (ja) * | 2001-12-14 | 2005-09-28 | 株式会社資生堂 | 毛髪化粧料 |
| JP3701237B2 (ja) * | 2001-12-14 | 2005-09-28 | 株式会社資生堂 | 化粧料組成物 |
| JP4590186B2 (ja) | 2004-01-14 | 2010-12-01 | 株式会社資生堂 | しわ改善用皮膚外用剤 |
| TW200526262A (en) * | 2004-01-14 | 2005-08-16 | Shiseido Co Ltd | Skin preparations for external use for wrinkle diminution |
| JP4819332B2 (ja) * | 2004-08-25 | 2011-11-24 | 株式会社 資生堂 | 毛髪化粧料 |
-
2007
- 2007-11-13 JP JP2007294276A patent/JP4450427B2/ja not_active Expired - Fee Related
-
2008
- 2008-11-12 US US12/742,444 patent/US8642023B2/en not_active Expired - Fee Related
- 2008-11-12 WO PCT/JP2008/070611 patent/WO2009063917A1/ja not_active Ceased
- 2008-11-12 CN CN2008801246410A patent/CN101917964B/zh not_active Expired - Fee Related
- 2008-11-12 KR KR1020107012987A patent/KR20100101104A/ko not_active Abandoned
- 2008-11-12 EP EP08848813.5A patent/EP2221046A4/en not_active Withdrawn
-
2014
- 2014-01-08 US US14/150,098 patent/US20140120051A1/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| KR20100101104A (ko) | 2010-09-16 |
| JP2009120510A (ja) | 2009-06-04 |
| US20110002873A1 (en) | 2011-01-06 |
| EP2221046A4 (en) | 2015-07-01 |
| US20140120051A1 (en) | 2014-05-01 |
| EP2221046A1 (en) | 2010-08-25 |
| CN101917964B (zh) | 2012-09-26 |
| HK1146580A1 (en) | 2011-06-24 |
| US8642023B2 (en) | 2014-02-04 |
| CN101917964A (zh) | 2010-12-15 |
| WO2009063917A1 (ja) | 2009-05-22 |
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