WO2023181682A1 - ポリグリセリンと脂肪酸及びジカルボン酸をエステル化した化合物 - Google Patents
ポリグリセリンと脂肪酸及びジカルボン酸をエステル化した化合物 Download PDFInfo
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- WO2023181682A1 WO2023181682A1 PCT/JP2023/004240 JP2023004240W WO2023181682A1 WO 2023181682 A1 WO2023181682 A1 WO 2023181682A1 JP 2023004240 W JP2023004240 W JP 2023004240W WO 2023181682 A1 WO2023181682 A1 WO 2023181682A1
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- Prior art keywords
- oil
- acid
- polyglycerin
- fatty acids
- compound
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- 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
- A61K8/72—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
- A61K8/86—Polyethers
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/34—Esters of acyclic saturated polycarboxylic acids having an esterified carboxyl group bound to an acyclic carbon atom
- C07C69/40—Succinic acid esters
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/34—Esters of acyclic saturated polycarboxylic acids having an esterified carboxyl group bound to an acyclic carbon atom
- C07C69/44—Adipic acid esters
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/34—Esters of acyclic saturated polycarboxylic acids having an esterified carboxyl group bound to an acyclic carbon atom
- C07C69/50—Sebacic acid esters
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/52—Esters of acyclic unsaturated carboxylic acids having the esterified carboxyl group bound to an acyclic carbon atom
- C07C69/533—Monocarboxylic acid esters having only one carbon-to-carbon double bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/52—Esters of acyclic unsaturated carboxylic acids having the esterified carboxyl group bound to an acyclic carbon atom
- C07C69/533—Monocarboxylic acid esters having only one carbon-to-carbon double bond
- C07C69/58—Esters of straight chain acids with eighteen carbon atoms in the acid moiety
Definitions
- the present invention relates to compounds obtained by esterifying polyglycerin with fatty acids and dicarboxylic acids, compositions containing the compounds, and cosmetics containing these.
- An oil-based cleansing cosmetic has been proposed (Patent Document 1).
- An object of the present invention is to provide a novel compound that is less irritating to the eyes and has excellent stability without separating when blended into ester oil.
- the present invention relates to the following [1] to [3].
- [1] A compound that is an ester of polyglycerin, fatty acid, and dicarboxylic acid, and satisfies the following (A) to (D).
- (A) Average degree of polymerization of polyglycerin is 2 to 20
- C The mass ratio of polyglycerin to fatty acid (polyglycerin:fatty acid) is 1:0.7 ⁇ 1:1.5
- the dicarboxylic acid has 4 to 12 carbon atoms, and the molar ratio to polyglycerin (dicarboxylic acid/polyglycerin) is 0.01 to 0.30.
- [3] A cosmetic containing the compound described in [1] or the composition described in [2].
- the inventors of the present invention have diligently studied the above-mentioned problems and found that by using a specific polyglycerin and esters of fatty acids and dicarboxylic acids, it has less eye irritation and is stable without separating when blended into ester oil. I discovered something new. Although such a mechanism is unknown, it is presumed that unsaturated fatty acids and branched fatty acids, which account for a large proportion of the constituent fatty acids in the compound of the present invention, have low eye irritation.
- the compound of the present invention is an ester of polyglycerin, fatty acid, and dicarboxylic acid, and satisfies the following (A) to (D).
- A) Average degree of polymerization of polyglycerin is 2 to 20
- B) The total proportion of unsaturated fatty acids and branched fatty acids having 18 to 22 carbon atoms among all fatty acids is 70% by mass or more
- C) The mass ratio of polyglycerin to fatty acid (polyglycerin:fatty acid) is 1:0.7 ⁇ 1:1.5
- the dicarboxylic acid has 4 to 12 carbon atoms, and the molar ratio to polyglycerin (dicarboxylic acid/polyglycerin) is 0.01 to 0.30.
- the average degree of polymerization of the polyglycerin according to the compound of the present invention is from 2 to 20, preferably from 3 to 20, more preferably from 4 to 10, from the viewpoint of usability and stability.
- the average degree of polymerization of polyglycerin in this specification is the average degree of polymerization of polyglycerin calculated from the hydroxyl value according to the terminal group analysis method, and is the average degree of polymerization calculated from (Formula 1) and (Formula 2). .
- the fatty acids related to the compound of the present invention include unsaturated fatty acids and branched fatty acids having 18 to 22 carbon atoms (that is, straight chain unsaturated fatty acids, branched chain saturated fatty acids, and branched chain unsaturated fatty acids).
- the total proportion of unsaturated fatty acids and branched fatty acids having 18 to 22 carbon atoms in the fatty acids related to the compounds of the present invention is 70% by mass or more, preferably 75% by mass or more of the total fatty acids. ⁇ 100% by weight, more preferably 85 ⁇ 100% by weight.
- Examples of unsaturated fatty acids and branched fatty acids having 18 to 22 carbon atoms include isostearic acid, oleic acid, linoleic acid, linolenic acid, ricinoleic acid, and erucic acid, and one or more of them can be contained.
- Fatty acids related to the compound of the present invention include unsaturated fatty acids and branched fatty acids having 18 to 22 carbon atoms, as well as saturated fatty acids, hydroxy fatty acids, and polymers and copolymers thereof, preferably those having 14 carbon atoms. ⁇ 24 saturated fatty acids and hydroxy fatty acids having 9 to 22 carbon atoms, and the degree of polymerization in polymers and copolymers is preferably 2 to 8, more preferably 5 to 8. Specifically, myristic acid, palmitic acid, stearic acid, hydroxystearic acid, polyhydroxystearic acid, etc. can be mentioned, and one type or two or more types can be contained. From the viewpoint of usability and stability, these fatty acids account for preferably 0 to 30% by mass, preferably 0 to 25% by mass, and more preferably 0 to 15% by mass of the total fatty acids.
- the mass ratio of polyglycerin and fatty acid (polyglycerin:fatty acid) in the compound of the present invention is 1:0.7 to 1:1.5, preferably 1:0.7, from the viewpoint of usability and stability. ⁇ 1:1.2.
- dicarboxylic acids related to the compound of the present invention include linear or branched saturated or unsaturated dicarboxylic acids having 4 to 12 carbon atoms. Specifically, succinic acid, maleic acid, adipic acid, sebacic acid, dodecanedioic acid, etc. may be mentioned, and one type or two or more types can be contained.
- the molar ratio of dicarboxylic acid to polyglycerin (dicarboxylic acid/polyglycerin) in the compound of the present invention is from 0.01 to 0.30, preferably from 0.1 to 0.30, from the viewpoint of usability and stability. 27 is preferably 0.15 to 0.24.
- the compound of the present invention can be obtained by subjecting the above-mentioned polyglycerin to a fatty acid and a dicarboxylic acid to an esterification reaction using a general synthesis method for polyglycerol fatty acid esters, and may be further purified according to known methods. .
- it can be produced by adding a catalyst such as an alkali to polyglycerin, fatty acid, and dicarboxylic acid as raw materials, and performing an esterification reaction at 200° C. or higher under normal pressure or reduced pressure.
- the compound of the present invention has low eye irritation and is excellent in stability without separating when blended with ester oil, so it can be suitably used in oil-based cosmetics using ester oil. It can also be used in non-oily cosmetics such as oil-based cosmetics using oils other than oil and emulsified cosmetics. It can be used in a wide range of cosmetics, including skin care products, skin cleansers, makeup cosmetics, and hair cosmetics. Examples include cleansing oil, cleansing oil gel, cleansing balm, cleansing milk, cleansing liquid, emulsion, body milk, bath oil, bath milk, hair oil, hair balm, and the like. Note that the compound of the present invention is not limited to use in cosmetics, and may be used in other uses.
- the present invention also discloses a composition containing the compound of the present invention and an oil agent.
- the content of the compound of the present invention in the composition of the present invention is preferably 0.05 to 30% by mass, more preferably 0.05 to 25% by mass.
- the content of the compound of the present invention in the composition of the present invention is preferably 1 to 30 parts by mass, more preferably 2 to 25 parts by mass, based on 100 parts by mass of the oil agent.
- oils examples include ester oils, hydrocarbon oils, animal and vegetable oils, silicone oils, higher alcohols, fatty acids, and waxes, and preferably ester oils, hydrocarbon oils, and animal and vegetable oils.
- Ester oils include diethylhexyl adipate, diisopropyl adipate, diisobutyl adipate, di2-hexyldecyl adipate, diheptyl undecyl adipate, avocado oil fatty acid ethyl, alkyl benzoate, isostearylglyceryl, hexyldecyl isostearate.
- hydrocarbon oil examples include isododecane, hydrogenated polyisobutene, squalane, ceresin, paraffin, pristane, liquid paraffin, liquid isoparaffin vaseline, and the like, with liquid paraffin being preferred.
- animal and vegetable oils include avocado oil, flaxseed oil, argan oil, almond oil, perilla oil, olive oil, orange roughy oil, cacao butter, carrot oil, cucumber oil, beef tallow, coconut oil, grapeseed oil, sesame oil, wheat germ oil, Rice bran oil, sasanqua oil, safflower oil, shea butter, soybean oil, turtle oil, clove oil, tea oil, evening primrose oil, camellia oil, corn oil, lard, rapeseed oil, coix oil, palm oil, palm kernel oil, Peanut oil, castor oil, sunflower oil, hazelnut oil, macadamia nut oil, mink oil, meadowfoam oil, cottonseed oil, coconut oil, rosehip oil, milk fat, adlay oil, jojoba oil, lavender oil, egg yolk oil, rice oil, lanolin, Rosemary oil is mentioned, and preferred are olive oil, safflower oil, camellia oil, rapeseed oil, palm oil, castor oil, sunflower oil,
- the preferred range of the content of the oil agent in the composition of the present invention varies depending on the use.
- the content of the oil agent in the composition for oil-based cosmetics can be 35-99% by mass, 50-98% by mass, etc.
- the content of the oil agent in the composition for emulsified cosmetics can be, for example, 0.1 to 20% by mass, 0.5 to 15% by mass, etc.
- composition of the present invention may further contain polyglycerol fatty acid ester in addition to the above components.
- polyglycerol fatty acid esters having unsaturated fatty acids and/or branched fatty acids having 18 to 22 carbon atoms are preferred.
- the HLB of the polyglycerin fatty acid ester is preferably 2 to 18, more preferably 5 to 13.
- Such polyglycerol fatty acid esters include polyglyceryl-2 oleate, polyglyceryl-2 sesquioleate, polyglyceryl-5 oleate, polyglyceryl-5 dioleate, polyglyceryl-5 trioleate, polyglyceryl-10 stearate, and polyglyceryl-5 oleate.
- Examples include polyglyceryl-10, polyglyceryl-10 dioleate, polyglyceryl-10 pentaoleate, and polyglyceryl-10 diisostearate.
- the content of the polyglycerin fatty acid ester is preferably 0.05 to 20% by mass, more preferably 0.1 to 15% by mass.
- composition of the present invention can optionally further contain other components depending on the intended use.
- a cosmetic composition in addition to the various ingredients listed above, water, surfactants, polyhydric alcohols, aqueous gelling agents, oily gelling agents, powder, antioxidants, colorants, chelates, etc.
- used in cosmetics such as agents, refreshing agents, thickeners, plant extracts, vitamins, neutralizers, moisturizers, anti-inflammatory agents, pH adjusters, amino acids, ultraviolet absorbers, preservatives, antibacterial agents, fragrances, etc.
- the composition may further contain optional ingredients.
- polyhydric alcohols examples include glycerin, diglycerin, triglycerin, polyglycerin, 1,3-butylene glycol, propylene glycol, dipropylene glycol, ethylene glycol, diethylene glycol, polyethylene glycol, pentanediol, isoprene glycol, erythritol, sorbitol, and polyhydric alcohol.
- examples include toll, lactose, fructose, maltose, etc., with glycerin and diglycerin being preferred.
- Thickeners include (behenic acid/eicosandioic acid) glyceryl, (behenic acid/eicosandioic acid) polyglyceryl-10, dextrin palmitate, inulin stearate, dextrin myristate, polyglyceryl octadeca (behenic acid/hydroxystearic acid). -20 etc.
- composition of the present invention can be prepared by mixing the compound of the present invention and an oil agent in a conventional manner.
- composition of the present invention can be suitably used in oil-based cosmetics, but it can also be used in non-oil-based cosmetics such as emulsified cosmetics. Further, the composition of the present invention may be used as a cosmetic as it is, or may be made into a cosmetic by further containing the above-mentioned optional ingredients. Note that the composition of the present invention is not limited to use in cosmetics, and may be used in other uses.
- Examples of the method for producing the cosmetic of the present invention include a method that includes a step of containing each of the above-mentioned components.
- the "step of incorporating the above-mentioned components" includes not only a mode in which a pre-prepared composition of the present invention is added, but also a mode in which the above-mentioned components are individually blended.
- the present invention also discloses a method for reducing the eye irritation, a method for improving the usability, and a method for improving the stability of an oil-based cosmetic, which includes the step of incorporating each of the above-mentioned components.
- oil-based cosmetics obtained in Preparation of Oil-based Cosmetics 1 to 6 were evaluated for stability, feel upon washing off, and eye irritation. In addition, for those with stability evaluation of "x”, evaluation of feel during washing and eye irritation was not performed and was written as "-".
- the oil-based cosmetics of Examples 1 to 22 using Compounds 1 to 17 all had little eye irritation and were stable without separating when blended with ester oil. It was excellent. Regarding the feel upon rinsing, even those with a rating of 1 were at a usable level. In addition, in Examples 1 and 22, it was confirmed that the degree of cloudiness during emulsification, water resistance, and emulsion particle size were also good, and the usability was visually good, it could be used with wet hands, and it was washable. I found out that it has excellent sex. Furthermore, as shown in Tables 9 to 13, it was found that it can be used for oils other than ester oils.
- the cosmetics of Formulation Examples 1 to 19 were all excellent in eye irritation and stability, and had a good feel when washed off.
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Abstract
Description
[1]ポリグリセリンと脂肪酸及びジカルボン酸のエステルであって、下記(A)~(D)を満たす、化合物。
(A)ポリグリセリンの平均重合度が2~20
(B)全脂肪酸のうち、炭素数18~22の不飽和脂肪酸及び分岐脂肪酸の合計割合が70質量%以上
(C)ポリグリセリンと脂肪酸の質量比(ポリグリセリン:脂肪酸)が1:0.7~1:1.5
(D)ジカルボン酸の炭素数が4~12であり、ポリグリセリンに対するモル比(ジカルボン酸/ポリグリセリン)が0.01~0.30
[2][1]記載の化合物と油剤を含有する、組成物。
[3][1]記載の化合物又は[2]記載の組成物を含有する、化粧料。
(A)ポリグリセリンの平均重合度が2~20
(B)全脂肪酸のうち、炭素数18~22の不飽和脂肪酸及び分岐脂肪酸の合計割合が70質量%以上
(C)ポリグリセリンと脂肪酸の質量比(ポリグリセリン:脂肪酸)が1:0.7~1:1.5
(D)ジカルボン酸の炭素数が4~12であり、ポリグリセリンに対するモル比(ジカルボン酸/ポリグリセリン)が0.01~0.30
(式1)平均重合度=(112.2×103-18×水酸基価)/(74×水酸基価-56.1×103)
(式2)水酸基価=(a-b)×28.05/試料の採取量(g)
a:空試験による0.5N水酸化カリウム溶液の消費量(ml)
b:本試験による0.5N水酸化カリウム溶液の消費量(ml)
上記(式1)中の水酸基価は社団法人日本油化学会編「日本油化学会制定 基準油脂分析試験法(I)1996年度版」に準じて(式2)で算出される。」
表1~3に示すように、脂肪酸、ジカルボン酸、ポリグリセリンを反応フラスコに入れ、アルカリ触媒を加え、260℃でエステル化反応することにより化合物を得た。化合物の酸価はすべて1以下であった。
ジカルボン酸を用いない以外は上記と同様にして、化合物を得た。
(C18-22不飽和または分岐脂肪酸(1)の項)
isoC18:イソステアリン酸
C18:1:オレイン酸
(その他脂肪酸(2)の項)
C18:ステアリン酸
C18OH:ヒドロキシステアリン酸
C18OH(6):ポリヒドロキシステアリン酸(重合度:6)
(ジカルボン酸の項)
C10:セバシン酸
C4:コハク酸
C6:アジピン酸
実施例1~17、比較例1~7
表4~6に示すように、表1~3で調製した化合物15gとエチルヘキサン酸セチル(エキセパールHO/花王株式会社)85gを70℃で加熱溶解し、室温まで攪拌冷却して油性化粧料を調製した。
実施例18~21
表7に示すように、表1~3で調製した化合物以外にポリグリセリン脂肪酸エステルを併用した以外は調製1と同様にして油性化粧料を調製した。
実施例22
表8に示すように、エチルヘキサン酸セチルに代えて、ミリスチン酸イソセチル(NIKKOL ICM-R/日光ケミカルズ)及びラウリン酸ヘキシル(SR CRODAMOL HL/クローダジャパン)を用いた以外は調製1と同様にして油性化粧料を調製した。
実施例23~39、比較例8~14
9~11に示すように、上記で調製した化合物15gと流動パラフィン(モレスコホワイトP-70/株式会社MORESCO)85gを70℃で加熱溶解し、室温まで攪拌冷却して油性化粧料を調製した。
実施例40、41
表12に示すように、上記で調製した化合物とポリグリセリン脂肪酸エステル計15gと、オリーブ油(CROPURE OL-LQ-(JP)/クローダジャパン株式会社)85gを70℃で加熱溶解し、室温まで攪拌冷却して油性化粧料を調製した。
実施例42、43
表13に示すように、上記で調製した化合物とポリグリセリン脂肪酸エステル計15gと、トリ(カプリル酸/カプリン酸)グリセリル(サンオイルMCT-7/太陽化学株式会社)85gを70℃で加熱溶解し、室温まで攪拌冷却して油性化粧料を調製した。
油性化粧料10gをバイアル瓶(容量20ml、内径2.5cm)に入れ、安定性を下記評価基準で評価した。結果を表4~13に示す。
(評価基準)
○:濁りや分離が見られない
×:分離している
油性化粧料1gを手の甲に塗布し、30秒間マッサージした後、水ですすいだ直後の肌感触を下記評価基準で評価した。評価は13名の専門パネラーで行い、13人中10人以上が○と回答したものを「3」、13人中8~9人が○と回答したものを「2」、13人中7人以下が○と回答したものを「1」とした。結果を表4~11に示す。
(評価基準)
○:べとつきがなく、さっぱりする
△:わずかにべとつきが残る
×:べとつく
適量の油性化粧料を眼元に馴染ませた時の眼刺激性を下記評価基準で評価した。評価は13名の専門パネラーで行い、13人中10人以上が○と回答したものを「3」、13人中8~9人が○と回答したものを「2」、13人中7人以下が○と回答したものを「1」とした。結果を表4~11に示す。
(評価基準)
○:眼が痛くない
△:わずかに眼が痛い
×:眼が痛い
油性化粧料0.1gを人工皮革に塗り広げる。水での洗い流しを想定し、2gの水を人工皮革に注ぐ。この時の白濁度合いを目視で確認し評価した。結果を表4、8に示す。
(評価基準)
3:白濁に乳化する
2:やや白濁に乳化する
1:白濁に乳化しない
水で濡れた手での使用を想定し、油性化粧料をバイアル瓶(容量20ml、内径2.5cm)に5g入れ、少量ずつ水を添加しながら攪拌を行ったものを調製し、目視にて透明を維持する限界加水率を下記式より求め、下記基準により評価した。結果を表4、8に示す。
加水率(%)=加水量(g)/5×100
(評価基準)
◎:加水率30%以上
〇:加水率20-30%未満
△:加水率10-20%未満
×:10%未満
油性化粧料をバイアル瓶(容量100ml、内径3.2cm)に1g入れた。水を99g添加し20回の振とう後、粒度分布計(BECKMAN COULTER LS 13 320)により粒度分布を測定した。求められる平均径を乳化粒子径とした。結果を表4、8に示す。
以下に、本発明の化粧料の処方例を挙げる。本発明はこの処方例によって何ら限定されるものではない。なお、配合量は全て製品全量に対する質量%で表している。
Claims (4)
- ポリグリセリンと脂肪酸及びジカルボン酸のエステルであって、下記(A)~(D)を満たす、化合物。
(A)ポリグリセリンの平均重合度が2~20
(B)全脂肪酸のうち、炭素数18~22の不飽和脂肪酸及び分岐脂肪酸の合計割合が70質量%以上
(C)ポリグリセリンと脂肪酸の質量比(ポリグリセリン:脂肪酸)が1:0.7~1:1.5
(D)ジカルボン酸の炭素数が4~12であり、ポリグリセリンに対するモル比(ジカルボン酸/ポリグリセリン)が0.01~0.30 - ジカルボン酸が、コハク酸、マレイン酸、アジピン酸、セバシン酸、及びドデカン二酸からなる群より選択される1種以上である、請求項1記載の化合物。
- 請求項1又は2記載の化合物と油剤を含有する、組成物。
- 請求項1又は2記載の化合物又は請求項3記載の組成物を含有する、化粧料。
Priority Applications (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP23774281.2A EP4506331A4 (en) | 2022-03-25 | 2023-02-08 | POLYGLYCEROL, FATTY ACID AND DICARBOXYLIC ACID ESTERIFICATION COMPOUND |
| JP2023536886A JP7346772B1 (ja) | 2022-03-25 | 2023-02-08 | ポリグリセリンと脂肪酸及びジカルボン酸をエステル化した化合物 |
| US18/844,103 US12491150B2 (en) | 2022-03-25 | 2023-02-08 | Compound in which polyglycerol, fatty acid, and dicarboxylic acid have been esterified |
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| JP2022-050592 | 2022-03-25 | ||
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| WO2023181682A1 true WO2023181682A1 (ja) | 2023-09-28 |
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| WO2022172645A1 (ja) * | 2021-02-10 | 2022-08-18 | 太陽化学株式会社 | ポリグリセリンと脂肪酸及びジカルボン酸をエステル化した化合物 |
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| JPS5640605A (en) * | 1979-09-11 | 1981-04-16 | Shiseido Co Ltd | Cosmetic |
| JPS5927807A (ja) * | 1982-08-04 | 1984-02-14 | Shiseido Co Ltd | 化粧料 |
| JPH07223925A (ja) * | 1994-02-10 | 1995-08-22 | Noevir Co Ltd | 口唇用化粧料 |
| JPH10265324A (ja) * | 1997-03-25 | 1998-10-06 | Noevir Co Ltd | 油性化粧料 |
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| JP2006273753A (ja) * | 2005-03-29 | 2006-10-12 | Sakamoto Yakuhin Kogyo Co Ltd | 透明粘性油及びこれを配合する化粧料 |
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