JP5960245B2 - 4−(3−エトキシ−4−ヒドロキシフェニル)−2−ブタノンおよび親油性溶媒を含む化粧料組成物 - Google Patents
4−(3−エトキシ−4−ヒドロキシフェニル)−2−ブタノンおよび親油性溶媒を含む化粧料組成物 Download PDFInfo
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- JP5960245B2 JP5960245B2 JP2014501622A JP2014501622A JP5960245B2 JP 5960245 B2 JP5960245 B2 JP 5960245B2 JP 2014501622 A JP2014501622 A JP 2014501622A JP 2014501622 A JP2014501622 A JP 2014501622A JP 5960245 B2 JP5960245 B2 JP 5960245B2
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- hydroxyphenyl
- ethoxy
- butanone
- organic solvent
- Prior art date
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- 239000002537 cosmetic Substances 0.000 title claims description 9
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- -1 3-ethoxy-4-hydroxyphenyl Chemical group 0.000 claims description 20
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- 230000000694 effects Effects 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- IIEWJVIFRVWJOD-UHFFFAOYSA-N ethyl cyclohexane Natural products CCC1CCCCC1 IIEWJVIFRVWJOD-UHFFFAOYSA-N 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 125000001153 fluoro group Chemical group F* 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 239000003205 fragrance Substances 0.000 description 1
- 239000003349 gelling agent Substances 0.000 description 1
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 1
- 229940100242 glycol stearate Drugs 0.000 description 1
- 239000008169 grapeseed oil Substances 0.000 description 1
- 239000010468 hazelnut oil Substances 0.000 description 1
- IUJAMGNYPWYUPM-UHFFFAOYSA-N hentriacontane Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC IUJAMGNYPWYUPM-UHFFFAOYSA-N 0.000 description 1
- 241000411851 herbal medicine Species 0.000 description 1
- MNWFXJYAOYHMED-UHFFFAOYSA-N hexane carboxylic acid Natural products CCCCCCC(O)=O MNWFXJYAOYHMED-UHFFFAOYSA-N 0.000 description 1
- 229940051250 hexylene glycol Drugs 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- LTYSCLBTUYRCBF-UHFFFAOYSA-N icosan-9-yl 2-hydroxyoctadecanoate Chemical compound CCCCCCCCCCCCCCCCC(O)C(=O)OC(CCCCCCCC)CCCCCCCCCCC LTYSCLBTUYRCBF-UHFFFAOYSA-N 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 239000001282 iso-butane Substances 0.000 description 1
- 229940100554 isononyl isononanoate Drugs 0.000 description 1
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 229940060384 isostearyl isostearate Drugs 0.000 description 1
- 229940119170 jojoba wax Drugs 0.000 description 1
- 235000019388 lanolin Nutrition 0.000 description 1
- 229940039717 lanolin Drugs 0.000 description 1
- JXNPEDYJTDQORS-UHFFFAOYSA-N linoleyl alcohol Natural products CCCCCC=CCC=CCCCCCCCCO JXNPEDYJTDQORS-UHFFFAOYSA-N 0.000 description 1
- 229940057995 liquid paraffin Drugs 0.000 description 1
- 239000010469 macadamia oil Substances 0.000 description 1
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 1
- 235000019341 magnesium sulphate Nutrition 0.000 description 1
- 238000003760 magnetic stirring Methods 0.000 description 1
- 230000000813 microbial effect Effects 0.000 description 1
- 239000004200 microcrystalline wax Substances 0.000 description 1
- 235000019808 microcrystalline wax Nutrition 0.000 description 1
- 239000004005 microsphere Substances 0.000 description 1
- 235000013336 milk Nutrition 0.000 description 1
- 239000008267 milk Substances 0.000 description 1
- 210000004080 milk Anatomy 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 1
- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 1
- CXQXSVUQTKDNFP-UHFFFAOYSA-N octamethyltrisiloxane Chemical compound C[Si](C)(C)O[Si](C)(C)O[Si](C)(C)C CXQXSVUQTKDNFP-UHFFFAOYSA-N 0.000 description 1
- WWZKQHOCKIZLMA-UHFFFAOYSA-M octanoate Chemical compound CCCCCCCC([O-])=O WWZKQHOCKIZLMA-UHFFFAOYSA-M 0.000 description 1
- 229960002446 octanoic acid 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
- 229940055577 oleyl alcohol Drugs 0.000 description 1
- XMLQWXUVTXCDDL-UHFFFAOYSA-N oleyl alcohol Natural products CCCCCCC=CCCCCCCCCCCO XMLQWXUVTXCDDL-UHFFFAOYSA-N 0.000 description 1
- 125000005702 oxyalkylene group Chemical group 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 235000019809 paraffin wax Nutrition 0.000 description 1
- 235000011837 pasties Nutrition 0.000 description 1
- 229940100460 peg-100 stearate Drugs 0.000 description 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical class OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
- WCVRQHFDJLLWFE-UHFFFAOYSA-N pentane-1,2-diol Chemical compound CCCC(O)CO WCVRQHFDJLLWFE-UHFFFAOYSA-N 0.000 description 1
- 230000002085 persistent effect Effects 0.000 description 1
- 229940066842 petrolatum Drugs 0.000 description 1
- 239000012071 phase Substances 0.000 description 1
- 229940057874 phenyl trimethicone Drugs 0.000 description 1
- 239000000419 plant extract Substances 0.000 description 1
- 238000004987 plasma desorption mass spectroscopy Methods 0.000 description 1
- 229920001921 poly-methyl-phenyl-siloxane Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229940100518 polyglyceryl-4 isostearate Drugs 0.000 description 1
- 230000002335 preservative effect Effects 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 210000004761 scalp Anatomy 0.000 description 1
- 229920002545 silicone oil Polymers 0.000 description 1
- 229940010747 sodium hyaluronate 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
- 230000007928 solubilization Effects 0.000 description 1
- 238000005063 solubilization Methods 0.000 description 1
- 239000003549 soybean oil Substances 0.000 description 1
- 235000012424 soybean oil Nutrition 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000002600 sunflower oil Substances 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- OULAJFUGPPVRBK-UHFFFAOYSA-N tetratriacontan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCO OULAJFUGPPVRBK-UHFFFAOYSA-N 0.000 description 1
- 229940042585 tocopherol acetate Drugs 0.000 description 1
- LINXHFKHZLOLEI-UHFFFAOYSA-N trimethyl-[phenyl-bis(trimethylsilyloxy)silyl]oxysilane Chemical compound C[Si](C)(C)O[Si](O[Si](C)(C)C)(O[Si](C)(C)C)C1=CC=CC=C1 LINXHFKHZLOLEI-UHFFFAOYSA-N 0.000 description 1
- PHYFQTYBJUILEZ-IUPFWZBJSA-N triolein Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCC(OC(=O)CCCCCCC\C=C/CCCCCCCC)COC(=O)CCCCCCC\C=C/CCCCCCCC PHYFQTYBJUILEZ-IUPFWZBJSA-N 0.000 description 1
- COXJMKGEQAWXNP-UHFFFAOYSA-N tris(14-methylpentadecyl) 2-hydroxypropane-1,2,3-tricarboxylate Chemical compound CC(C)CCCCCCCCCCCCCOC(=O)CC(O)(C(=O)OCCCCCCCCCCCCCC(C)C)CC(=O)OCCCCCCCCCCCCCC(C)C COXJMKGEQAWXNP-UHFFFAOYSA-N 0.000 description 1
- 239000010497 wheat germ oil 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
- A61K8/34—Alcohols
- A61K8/347—Phenols
-
- 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
- A61K8/35—Ketones, e.g. benzophenone
-
- 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
- A61K8/37—Esters of carboxylic acids
-
- 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
- A61K8/37—Esters of carboxylic acids
- A61K8/375—Esters of carboxylic acids the alcohol moiety containing more than one hydroxy group
-
- 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
- A61K8/40—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
- A61K8/44—Aminocarboxylic acids or derivatives thereof, e.g. aminocarboxylic acids containing sulfur; Salts; Esters or N-acylated derivatives thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q1/00—Make-up preparations; Body powders; Preparations for removing make-up
- A61Q1/14—Preparations for removing make-up
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q19/00—Preparations for care of the skin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q5/00—Preparations for care of the hair
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)
- Emergency Medicine (AREA)
- Dermatology (AREA)
- Cosmetics (AREA)
Description
δ=(δ2=δd 2+δp 2+δh 2)1/2
式中、
- δdは、分子衝突の間に誘起される双極子の形成から生じるロンドン分散力を特徴付け、
- δpは、永久双極子間のデバイ相互作用力を特徴付け、
- δhは、特異的相互作用力(例えば水素結合、酸/塩基、供与体/受容体など)を特徴付ける。ハンセン三次元溶解度空間における溶媒の定義は、C.M.Hansen著の記事「The three-dimensional solubility parameters」、J.Paint Technol.39、105(1967)に記載されている。
4.5<δa<7および14<δd<17
6<δa<7および16<δd<17
- 植物由来の炭化水素ベースの油、例えば4〜10個の炭素原子を含有する脂肪酸の液体トリグリセリド、例えば、ヘプタン酸トリグリセリドまたはオクタン酸トリグリセリド、あるいは、例えば、ヒマワリ油、トウモロコシ油、ダイズ油、骨髄油、ブドウの種油、ゴマ油、ヘーゼルナッツ油、アンズ油、マカダミア油、アララ油、ヒマシ油、アボカド油、ホホバ油、およびシアバター油;
- 特に脂肪酸の合成エステルおよびエーテル、例えば式R1COOR2およびR1OR2(式中、R1は8〜29個の炭素原子を含む脂肪酸残基を表し、R2は3〜30個の炭素原子を含む分枝状または非分枝状の炭化水素ベースの鎖を表す)の油、例えばピュアセリンオイル(Purcellin oil)、イソノナン酸イソノニル、パルミチン酸2-エチルヘキシル、ステアリン酸2-オクチルドデシル、エルカ酸2-オクチルドデシルまたはイソステアリン酸イソステアリル;ヒドロキシル化エステル、例えば乳酸イソステアリル、ヒドロキシステアリン酸オクチル、ヒドロキシステアリン酸オクチルドデシル、リンゴ酸ジイソステアリルまたはクエン酸トリイソセチル;脂肪アルコールヘプタノエート、オクタノエートまたはデカノエート;ポリオールエステル、例えばジオクタン酸プロピレングリコール、ジヘプタン酸ネオペンチルグリコールおよびジイソノナン酸ジエチレングリコール;ならびにペンタエリスリトールエステル、例えばテトライソステアリン酸ペンタエリスリチル;
- 鉱物もしくは合成起源の直鎖状または分枝状の炭化水素、例えば揮発性もしくは不揮発性流動パラフィンおよびその誘導体、ワセリン、ポリデセン、ならびに水添ポリイソブテン、例えばパールリーム(Parleam)油;
- 8〜26個の炭素原子を含む脂肪アルコール、例えばセチルアルコール、ステアリルアルコールおよびこれらの混合物(セチルステアリルアルコール)、オクチルドデカノール、2-ブチルオクタノール、2-ヘキシルデカノール、2-ウンデシルペンタデカノール、オレイルアルコールまたはリノレイルアルコール;
- シリコーンオイル、例えば、室温で液体またはペースト状である、直鎖状もしくは環状のシリコーン鎖を有する揮発性または不揮発性のポリメチルシロキサン(PDMS)、特にシクロポリジメチルシロキサン(シクロメチコーン)、例えばシクロヘキサシロキサン; 2〜24個の炭素原子を含む、ペンダントであるもしくはシリコーン鎖の末端にあるアルキル基、アルコキシ基またはフェニル基を含むポリジメチルシロキサン;フェニルシリコーン、例えばフェニルトリメチコーン、フェニルジメチコーン、フェニルトリメチルシロキシジフェニルシロキサン、ジフェニルジメチコーン、ジフェニルメチルジフェニルトリシロキサンまたは2-フェニルエチルトリメチルシロキシシリケートおよびポリメチルフェニルシロキサン;
-これらの混合物。
4-(3-エトキシ-4-ヒドロキシフェニル)-2-ブタノンで溶解度試験を実施した。
試験溶媒中に溶解できる化合物の量は、このようにして求めた。最大値は、エステル化合物が、評価される溶媒中にそれ以上は溶解しなくなる量に相当する。
したがって、安息香酸2-フェニルエチル、N-ラウロイルサルコシンイソプロピルおよびカプリン酸/カプリル酸トリグリセリドなどの溶媒が活性薬剤を溶解したのに対して、パルミチン酸2-エチルヘキシル(δa=4.23;δd=16.20)および2-オクチルドデカノール(δa=7.70;δd=16.40)はあまり活性薬剤を溶解しなかったことが判明した。
キサンタンガム(Rhodia製のRhodicare XC) 0.15
ステアリン酸グリセリルおよびステアリン酸PEG-100の混合物
[Uniqema製のArlacel(登録商標)165 FL] 2.5
1,3-ブチレングリコール 0.525
ステアリルアルコール 1
ステアリン酸 1.2
カプリン酸/カプリル酸トリグリセリド
[Stearineries Dubois製の70/30 C8〜C10 Triglycerides(Dub MCT 7030)] 5
イソパラフィン/水中で40%の逆エマルションとしての
アクリルアミド/アクリルアミド-2-メチルプロパンスルホン酸ナトリウムコポリマー
(SEPPIC製のSepigel 305) 1.7
ヒアルロン酸ナトリウム(Soliance製のCristalhyal) 0.05
4-(3-エトキシ-4-ヒドロキシフェニル)-2-ブタノン 2
グリセロール 5
セチルアルコール 1
酢酸トコフェロール 0.2
シクロペンタシロキサン 5
水 100までの適量
パルミチン酸2-エチルヘキシル 7
クエン酸 0.06
グリセロール 3
キサンタンガム(CP Kelco製のKeltrol CG-T) 0.1
酢酸エチル/シクロヘキサン混合物中の
重合アクリル酸/メタクリル酸ステアリルコポリマー
(Noveon製のPemulen TR-1 Polymer) 0.1
4-(3-エトキシ-4-ヒドロキシフェニル)-2-ブタノン 2
トウモロコシ油、ぬか油、ゴマ油および小麦胚種油の混合物(29/40/20/10) 5
トリエタノールアミン 0.4
カルボキシビニルポリマー(3V製のSynthalen K) 0.3
イソパラフィン/水中で40%の逆エマルションとしての
アクリルアミド/アクリルアミド-2-メチルプロパンスルホン酸ナトリウムコポリマー
(SEPPIC製のSepigel 305) 0.5
水 100までの適量
エタノール 5
ポリジメチルシロキサン10cSt 6.75
アセチル化ステアリン酸エチレングリコールおよびトリステアリン酸グリセリルの混合物
(United Guardian製のUnitwix) 0.5
オクテニルコハク酸無水物でエステル化したコーンスターチのアルミニウム塩
(National Starch製のDry Flo Plus 28-1160) 3
シアバターの液体分率(Olvea製のShea Olein) 4
イソステアリン酸ポリグリセリル-4(Goldschmidt製のGI 34) 0.5
4-(3-エトキシ-4-ヒドロキシフェニル)-2-ブタノン 2
杏仁油 1.4
イソブタンで膨張された
塩化ビニリデン/アクリロニトリル/メタクリル酸メチルコポリマー微小球
(Expancel製のExpancel 551 DE 40 D42) 0.1
硫酸マグネシウム 0.7
水添ポリイソブテン
(NOF Corporation製のParleam) 10
カプリン酸/カプリル酸トリグリセリド
[Stearineries Dubois製の70/30 C8〜C10 Triglycerides(Dub MCT 7030)] 5
セチルジメチコーンコポリオール
(Goldschmidt製のAbil EM 90) 1.5
水 100までの適量
Claims (7)
- 生理学的に許容される油性媒体中に、
4-(3-エトキシ-4-ヒドロキシフェニル)-2-ブタノンと、ハンセン溶解度空間における溶解度パラメータが4.5<δa<7および14<δd<22になるような有機溶媒とを含む組成物であって、
前記生理学的に許容される油性媒体が油であり、
前記有機溶媒が、N-ラウロイルサルコシンイソプロピル、カプリン酸/カプリル酸トリグリセリド、安息香酸2-フェニルエチル、パルミチン酸イソプロピルおよびミリスチン酸イソプロピルから選択される、組成物。 - 前記有機溶媒が、N-ラウロイルサルコシンイソプロピルおよびカプリン酸/カプリル酸トリグリセリドから成る群から選択されることを特徴とする、請求項1に記載の組成物。
- 前記有機溶媒が、組成物の総質量に対して0.05質量%から30質量%の範囲の含有量で存在することを特徴とする、請求項1または2に記載の組成物。
- 4-(3-エトキシ-4-ヒドロキシフェニル)-2-ブタノンが、組成物の総質量に対して0.01質量%から10質量%の範囲の含有量で存在することを特徴とする、請求項1から3のいずれか一項に記載の組成物。
- 前記有機溶媒および4-(3-エトキシ-4-ヒドロキシフェニル)-2-ブタノンが、10以下の有機溶媒/4-(3-エトキシ-4-ヒドロキシフェニル)-2-ブタノンの質量比で存在することを特徴とする、請求項1から4のいずれか一項に記載の組成物。
- 油中水型または水中油型エマルションの形態であることを特徴とする、請求項1から5のいずれか一項に記載の組成物。
- ケラチン物質をケアおよび/またはメイクアップおよび/またはクレンジングするための非治療的な美容処置方法であって、請求項1から6のいずれか一項に記載の組成物を前記ケラチン物質に適用するステップを含む方法。
Applications Claiming Priority (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR1152788A FR2973228B1 (fr) | 2011-04-01 | 2011-04-01 | Composition cosmetique comprenant du 4-(3-ethoxy-4-hydroxyphenyl)butan-2-one |
FR1152788 | 2011-04-01 | ||
US201161499707P | 2011-06-22 | 2011-06-22 | |
US61/499,707 | 2011-06-22 | ||
PCT/EP2012/055658 WO2012130954A1 (en) | 2011-04-01 | 2012-03-29 | Cosmetic composition comprising 4-(3-ethoxy-4-hydroxyphenyl)-2-butanone and a lipophilic solvent |
Publications (2)
Publication Number | Publication Date |
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JP2014509627A JP2014509627A (ja) | 2014-04-21 |
JP5960245B2 true JP5960245B2 (ja) | 2016-08-02 |
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JP2014501622A Active JP5960245B2 (ja) | 2011-04-01 | 2012-03-29 | 4−(3−エトキシ−4−ヒドロキシフェニル)−2−ブタノンおよび親油性溶媒を含む化粧料組成物 |
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US (1) | US20140057997A1 (ja) |
EP (1) | EP2694023B1 (ja) |
JP (1) | JP5960245B2 (ja) |
KR (1) | KR101927560B1 (ja) |
CN (1) | CN104010620B (ja) |
BR (1) | BR112013025120B1 (ja) |
ES (1) | ES2587844T3 (ja) |
FR (1) | FR2973228B1 (ja) |
RU (1) | RU2589828C2 (ja) |
WO (1) | WO2012130954A1 (ja) |
Families Citing this family (24)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2973226B1 (fr) | 2011-04-01 | 2013-03-29 | Oreal | Utilisation de composes (ethoxy-hydroxyphenyl)alkylcetone ou ethoxyhydroxyalkylphenol pour traiter la peau grasse |
FR2973231B1 (fr) * | 2011-04-01 | 2013-12-20 | Oreal | Utilisation comme antipelliculaire de composes (ethoxyhydroxyphe-nyl)alkylcetone ou ethoxyhydroxyalkylphenol |
CN104869979B (zh) * | 2012-12-28 | 2018-08-10 | 莱雅公司 | 化妆品组合物、清洁角质的美容方法以及它们的用途 |
JP6291031B2 (ja) | 2013-04-05 | 2018-03-14 | ザ プロクター アンド ギャンブル カンパニー | 予め乳化させた製剤を含むパーソナルケア組成物 |
US9101551B2 (en) | 2013-10-09 | 2015-08-11 | The Procter & Gamble Company | Personal cleansing compositions and methods |
US10806688B2 (en) | 2014-10-03 | 2020-10-20 | The Procter And Gamble Company | Method of achieving improved volume and combability using an anti-dandruff personal care composition comprising a pre-emulsified formulation |
CN107106474B (zh) | 2014-11-10 | 2021-06-01 | 宝洁公司 | 具有两种有益相的个人护理组合物 |
CN107106429B (zh) | 2014-11-10 | 2021-06-29 | 宝洁公司 | 具有两种有益相的个人护理组合物 |
US10966916B2 (en) | 2014-11-10 | 2021-04-06 | The Procter And Gamble Company | Personal care compositions |
US9993404B2 (en) | 2015-01-15 | 2018-06-12 | The Procter & Gamble Company | Translucent hair conditioning composition |
MX2018008913A (es) | 2016-01-20 | 2019-05-06 | Procter & Gamble | Composicion acondicionadora del cabello que comprende eter monoalquil glicerilo. |
FR3053333B1 (fr) * | 2016-06-30 | 2018-07-27 | L'oreal | Melange liquide contenant du 4-(3-ethoxy-4-hydroxyphenyl)butan-2-one et un com-pose de niacinamide, et composition cosmetique le contenant |
FR3053334B1 (fr) | 2016-06-30 | 2018-07-27 | L'oreal | Melange liquide contenant du 4-(3-ethoxy-4-hydroxyphenyl)butan-2-one et de compose de xanthine |
EP3558234A1 (en) * | 2016-12-22 | 2019-10-30 | L'oreal | Preserving agent comprising 4-(3-ethoxy-4-hydroxyphenyl)-2-butanone, and use thereof in cosmetic compositions |
FR3068218B1 (fr) * | 2017-06-30 | 2019-08-16 | L'oreal | Melange antimicrobien contenant du 4-(3-ethoxy-4-hydroxyphenyl)butan-2-one et de la chlorphenesine, et composition cosmetique le contenant |
CN111050554B (zh) * | 2017-06-30 | 2021-12-10 | 莱雅公司 | 含4-(3-乙氧基-4-羟苯基)丁-2-酮的抗微生物混合物及含该抗微生物混合物的化妆品组合物 |
EP3644733B1 (en) * | 2017-06-30 | 2021-03-24 | L'Oreal | Antimicrobial mixture containing 4-(3-ethoxy-4-hydroxyphenyl)butan-2-one and an organic acid compound, and cosmetic composition containing same |
EP3697375B1 (en) | 2017-10-20 | 2021-12-01 | The Procter & Gamble Company | Aerosol foam skin cleanser |
WO2019079405A1 (en) | 2017-10-20 | 2019-04-25 | The Procter & Gamble Company | AEROSOL FOAMING CLEANSER FOR THE SKIN |
FR3072568B1 (fr) * | 2017-10-25 | 2019-09-27 | L'oreal | Composition cosmetique biphase comprenant une 4-(3-alcoxy-4-hydroxyphenyl)alkylcetone |
WO2019088056A1 (ja) * | 2017-10-31 | 2019-05-09 | 株式会社 資生堂 | 水中油型乳化固形化粧料 |
CN113015904B (zh) | 2018-11-29 | 2024-06-18 | 宝洁公司 | 用于筛选个人护理产品的方法 |
FR3103677B1 (fr) * | 2019-11-28 | 2022-05-27 | Oreal | Utilisation d’un composé de type 4-(3-éthoxy-4 hydroxyphényl) alkylcétone contre les bactéries du complexe Burkholderia cepacia |
FR3103678B1 (fr) * | 2019-12-03 | 2022-07-01 | Oreal | Composition contenant du 4-(3-éthoxy-4-hydroxyphényl)butan-2-one, un conservateur et/ou antioxydant, un tensioactif, et un polymère, le procédé de traitement des matières kératiniques à partir de la composition |
Family Cites Families (10)
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WO1989003376A1 (en) * | 1987-10-06 | 1989-04-20 | Tsumura Juntendo, Inc. | Keratosis-treating agent |
EP0545002A1 (en) | 1991-11-21 | 1993-06-09 | Kose Corporation | Silicone polymer, paste-like composition and water-in-oil type cosmetic composition comprising the same |
US5811487A (en) | 1996-12-16 | 1998-09-22 | Dow Corning Corporation | Thickening silicones with elastomeric silicone polyethers |
PT1156814E (pt) * | 1999-03-03 | 2004-01-30 | Eurovita A S | Compostos farmaceuticos suplementos dieteticos e composicoes cosmeticas compreendendo um acido gordo e gengibre |
US20040156799A1 (en) * | 2002-06-04 | 2004-08-12 | Zigang Dong | Cancer treatment method and compositions |
JP5464778B2 (ja) * | 2006-03-10 | 2014-04-09 | 花王株式会社 | 頭髪化粧料 |
US20100099766A1 (en) * | 2008-10-16 | 2010-04-22 | Novartis Ag | Topical NSAID compositions having sensate component |
FR2950884B1 (fr) * | 2009-10-01 | 2011-11-11 | Oreal | Utilisation de derives de vanilline comme conservateur, procede de conservation, composes et composition |
FR2951079B1 (fr) * | 2009-10-08 | 2012-04-20 | Oreal | Composition photoprotectrice a base d'un compose 2-alcoxy-4-alkylcetone phenol ; utilisation dudit compose pour augmenter le facteur de protection solaire |
DE102009055917A1 (de) * | 2009-11-27 | 2011-06-01 | Beiersdorf Ag | Verwendung von Zingeron gegen Altershaut |
-
2011
- 2011-04-01 FR FR1152788A patent/FR2973228B1/fr not_active Expired - Fee Related
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2012
- 2012-03-29 CN CN201280017169.7A patent/CN104010620B/zh active Active
- 2012-03-29 EP EP12710971.8A patent/EP2694023B1/en active Active
- 2012-03-29 JP JP2014501622A patent/JP5960245B2/ja active Active
- 2012-03-29 KR KR1020137028739A patent/KR101927560B1/ko active IP Right Grant
- 2012-03-29 US US14/007,549 patent/US20140057997A1/en active Pending
- 2012-03-29 RU RU2013148812/15A patent/RU2589828C2/ru active
- 2012-03-29 WO PCT/EP2012/055658 patent/WO2012130954A1/en active Application Filing
- 2012-03-29 BR BR112013025120-4A patent/BR112013025120B1/pt active IP Right Grant
- 2012-03-29 ES ES12710971.8T patent/ES2587844T3/es active Active
Also Published As
Publication number | Publication date |
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EP2694023B1 (en) | 2016-05-18 |
CN104010620A (zh) | 2014-08-27 |
RU2589828C2 (ru) | 2016-07-10 |
KR20140019426A (ko) | 2014-02-14 |
FR2973228B1 (fr) | 2014-08-01 |
RU2013148812A (ru) | 2015-05-10 |
CN104010620B (zh) | 2017-09-12 |
JP2014509627A (ja) | 2014-04-21 |
EP2694023A1 (en) | 2014-02-12 |
KR101927560B1 (ko) | 2018-12-10 |
FR2973228A1 (fr) | 2012-10-05 |
US20140057997A1 (en) | 2014-02-27 |
WO2012130954A1 (en) | 2012-10-04 |
BR112013025120B1 (pt) | 2018-04-24 |
BR112013025120A2 (pt) | 2016-08-16 |
ES2587844T3 (es) | 2016-10-27 |
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