JPS62143971A - Gelatinous composition - Google Patents
Gelatinous compositionInfo
- Publication number
- JPS62143971A JPS62143971A JP28493085A JP28493085A JPS62143971A JP S62143971 A JPS62143971 A JP S62143971A JP 28493085 A JP28493085 A JP 28493085A JP 28493085 A JP28493085 A JP 28493085A JP S62143971 A JPS62143971 A JP S62143971A
- Authority
- JP
- Japan
- Prior art keywords
- parts
- fatty acid
- weight
- composition
- formula
- 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
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
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/73—Polysaccharides
- A61K8/732—Starch; Amylose; Amylopectin; Derivatives thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/02—Cosmetics or similar toiletry preparations characterised by special physical form
- A61K8/04—Dispersions; Emulsions
- A61K8/042—Gels
-
- 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
- A61K8/58—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing atoms other than carbon, hydrogen, halogen, oxygen, nitrogen, sulfur or phosphorus
- A61K8/585—Organosilicon compounds
-
- 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
- A61K8/89—Polysiloxanes
- A61K8/891—Polysiloxanes saturated, e.g. dimethicone, phenyl trimethicone, C24-C28 methicone or stearyl dimethicone
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q19/00—Preparations for care of the skin
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Epidemiology (AREA)
- Birds (AREA)
- Emergency Medicine (AREA)
- Dermatology (AREA)
- Chemical & Material Sciences (AREA)
- Dispersion Chemistry (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Medicinal Preparation (AREA)
- Cosmetics (AREA)
Abstract
Description
【発明の詳細な説明】
(産業上の利用分野)
本発明はゲル状組成物、特にはシリカなどの充填剤を使
用しない、化粧品用基材などに有用とされるシリコーン
オイルを主材とするゲル状組成物に関するものである。Detailed Description of the Invention (Field of Industrial Application) The present invention is a gel-like composition, particularly a silicone oil that does not use fillers such as silica and is useful as a base material for cosmetics. The present invention relates to a gel composition.
(従来の技術)
化粧品用、医療用のペースト、クリーム、プレス状組成
物などには各種のシリコ−オイルが添加配合されている
が、シリコーン組成物を基材とする利用例は少ない。(Prior Art) Various silicone oils are added to pastes, creams, pressed compositions, etc. for cosmetics and medical purposes, but there are few examples of the use of silicone compositions as a base material.
これはシリコ−オイルをゲル状物とするには無機質充填
剤としての疎水性シリカ、ベントンなどの増粘剤の添加
が必要であり、使用するシリコ−オイルも25℃におけ
る粘度が100cS以上である比較的高粘度のものとす
る必要があるために、このようにして得られたゲル状物
を皮膚表面に塗布した場合には伸度感が重く、また揮発
分が殆んどないのでべたつき感が長期にわたって残留す
る不利があるからとされている。This is because to make silico oil into a gel-like substance, it is necessary to add thickeners such as hydrophobic silica and bentone as inorganic fillers, and the silico oil used also has a viscosity of 100 cS or more at 25°C. Because it needs to have a relatively high viscosity, when the gel-like material obtained in this way is applied to the skin surface, it feels heavy and sticky, and it has almost no volatile content, so it does not feel sticky. It is said that this is because there is a disadvantage of remaining for a long period of time.
したがって、これらの欠点を解決した低粘度で揮発性に
富むシリコーンを主剤とするゲル状組成物が待望されて
いる。Therefore, there is a long-awaited need for a gel-like composition based on silicone, which has low viscosity and high volatility, and which solves these drawbacks.
(発明の構成)
本発明は上記したような不利を解決したシリコーン系の
ゲル状組成物に関するものであり。これは、1)式
%式%)
示される環状ジメチルポリシロキサン30〜90重量部
、2)炭素数8〜24の脂肪酸と炭素数1〜24の脂肪
族アルコールとのエステルまたは炭素数10〜40の脂
肪族炭化水素から選択される1種または2種以上の混合
物5〜50重量部、3)デキストリン脂肪酸エステル5
〜30重量部とからなることを特徴とするものである。(Structure of the Invention) The present invention relates to a silicone-based gel composition that solves the above-mentioned disadvantages. This includes 1) 30 to 90 parts by weight of a cyclic dimethylpolysiloxane represented by the formula %), 2) an ester of a fatty acid having 8 to 24 carbon atoms and an aliphatic alcohol having 1 to 24 carbon atoms, or a cyclic dimethylpolysiloxane having 10 to 40 carbon atoms. 5 to 50 parts by weight of one or a mixture of two or more selected from aliphatic hydrocarbons, 3) Dextrin fatty acid ester 5
~30 parts by weight.
すなわち、本発明者らは特に化粧品用、医療用などに有
用とされるシリコーンオイルを主剤とするゲル状組成物
について種々検討した結果、シリコーンオイルとして上
記した式で示される環状ジメチルポリシロキサンを使用
すると共に、このゲル化剤として高級脂肪酸の脂肪族ア
ルコールとのエステルまたは脂肪族炭化水素とデキスト
リン脂肪酸エステルを使用すると所期のゲル状組成物が
容易に得られ、このゲル状組成物はこれを皮膚などに塗
布した場合に進展性が軽快で使用感もさっばりしており
、塗布後は環状ジメチルポリシロキサンが蒸発するため
に濡れ感覚が何時までも残ることがないということを確
認して本発明を完成させた。That is, the present inventors conducted various studies on gel compositions based on silicone oil, which are particularly useful for cosmetics and medical purposes, and found that cyclic dimethylpolysiloxane represented by the above formula was used as the silicone oil. In addition, when an ester of a higher fatty acid with an aliphatic alcohol or an aliphatic hydrocarbon and a dextrin fatty acid ester is used as the gelling agent, the desired gel composition can be easily obtained. We confirmed that when applied to the skin, it spreads easily and has a light feeling of use, and that the cyclic dimethylpolysiloxane evaporates after application, so the wet feeling does not remain for any length of time. Completed the invention.
本発明のゲル状組成物を構成する第1成分としてのシリ
コーンオイルは、式
で示される環状ジメチルポリシロキサンとされるが、こ
のものはこれを含有するゲル状組成物を使用後に発揮す
るものであることが望ましいので、このn値は3〜6の
ものとされる。なお、このものは1種の使用でもよく、
2種以上の混合物であってもよいが、この使用量はゲル
状組成物100重量部におけるこの第1成分の量が30
重量部以下では他成分が多くなりすぎて本組成物に期待
される軽快な進展性が乏しくなるし、べたつき感も増大
し、90重量部以上とすると十分なゲル化に至れなくな
るので、30〜90重量部の範囲とすることが必要とさ
れるが、この好ましい範囲は40〜85重量部とされる
。The silicone oil as the first component constituting the gel composition of the present invention is a cyclic dimethylpolysiloxane represented by the formula, and this oil exhibits its properties after using the gel composition containing it. Since it is desirable that the n value be 3 to 6. In addition, this item may be used as one type,
A mixture of two or more types may be used, but the amount used is such that the amount of the first component is 30 parts by weight in 100 parts by weight of the gel composition.
If it is less than 90 parts by weight, the amount of other components will be too large and the light spreadability expected of this composition will be poor, and the sticky feeling will increase, and if it is more than 90 parts by weight, sufficient gelation will not be achieved. A range of 90 parts by weight is required, with a preferred range of 40 to 85 parts by weight.
また、この組成物における第2成分は前記したように炭
素数が8〜20の高級脂肪酸と炭素数1〜24の脂肪族
アルコールとのエステルまたは炭素数10〜40の脂肪
族炭化水素とされ、これについてはミリスチン酸イソプ
ロピル、ミリスチン酸ブチル、ミリスチン酸ミリスチル
、ミリスチン酸オクチルデシル、インオクチル酸セチル
、オレイン酸デシル、ステアリン酸ブチル、ラウリン酸
ヘキシル、バルミチン酸イソプロピル、パルミチン酸ブ
チルなどの高級脂肪酸モノエステル、ジオレイン酸プロ
ピレングリコール、ジー2−エチルヘキサン酸ネオペン
チルグリコールなどの高級脂肪酸ジエステル、カプリル
酸トリグリセリド、カプリン酸トリグリセリドなどの高
級脂肪酸トリエステルなど、さらにはスクワラン、アイ
ソパー〔エクソン化学■製、脂肪族炭化水素系溶剤の商
品名〕などが例示されるが、これらはその1種で使用し
ても2種以上の混合物であってもよい。なお、この第2
成分の使用量はゲル化組成物100重量部中におけるこ
の第2成分の量が5重量部以下では第1成分としてのシ
リコーンオイルがゲル化するまでには至らず、50重量
部以上とすると得られるゲル状組成物が軽快な伸展性の
乏しいものとなり、べたつき感も増大するので5〜50
重量部の範囲とする必要があるが、この好ましい範囲は
7〜45重量部とされる。Further, the second component in this composition is an ester of a higher fatty acid having 8 to 20 carbon atoms and an aliphatic alcohol having 1 to 24 carbon atoms, or an aliphatic hydrocarbon having 10 to 40 carbon atoms, as described above. Higher fatty acid monoesters such as isopropyl myristate, butyl myristate, myristyl myristate, octyldecyl myristate, cetyl inoctylate, decyl oleate, butyl stearate, hexyl laurate, isopropyl valmitate, and butyl palmitate , higher fatty acid diesters such as propylene glycol dioleate and neopentyl glycol di-2-ethylhexanoate, higher fatty acid triesters such as caprylic acid triglyceride and capric acid triglyceride, as well as squalane, Isopar [manufactured by Exxon Chemical, aliphatic carbonization] Examples include [trade name of hydrogen-based solvent], but these may be used alone or in a mixture of two or more. Note that this second
If the amount of the second component in 100 parts by weight of the gelling composition is less than 5 parts by weight, the silicone oil as the first component will not gel, and if it is 50 parts by weight or more, it will be advantageous. The gel-like composition produced will have poor light extensibility and will have an increased sticky feel, so
The preferred range is 7 to 45 parts by weight.
つぎにこのゲル状組成物における第3成分としてのデキ
ストリン脂肪酸エステルは例えば構造式が次式
で示され、Aは水素原子または炭素数8〜20ののアシ
ル基で全Aモル数の50%以上はアシル基。Next, the dextrin fatty acid ester as the third component in this gel composition has, for example, a structural formula shown by the following formula, where A is a hydrogen atom or an acyl group having 8 to 20 carbon atoms and accounts for at least 50% of the total number of moles of A. is an acyl group.
Qは20〜30とされるものであり、この使用量はゲル
状組成物100重量部中におけるこの第3成分の量が5
重量部以下ではシリコーンオイルのゲル化が進まず、3
0重量部以上とすると得られる組成物が固くなりすぎて
伸展性の乏しいものとなるので5〜30重量部の範囲と
することが必要とされるが、この好ましい範囲は7〜2
5重量部とされる。Q is 20 to 30, and this usage amount is such that the amount of the third component in 100 parts by weight of the gel composition is 5.
Below 3 parts by weight, silicone oil will not gel.
If the amount is more than 0 parts by weight, the resulting composition will be too hard and have poor extensibility, so it is necessary to use it in the range of 5 to 30 parts by weight, but this preferred range is 7 to 2 parts by weight.
5 parts by weight.
本発明のゲル状組成物は上記した第1成分〜第3成分の
所定量を均一に混合することによって得ることかできる
が、この混合は50〜100°Cで行うことがよく、例
えば100℃以下で加温攪拌を行って前記した脂肪酸エ
ステルまたは脂肪族炭化水素およびデキストリン脂肪エ
ステルをシリコーンオイルに均一に溶解してから冷却す
れば目的とする均質なゲル状組成物を得ることができる
。The gel composition of the present invention can be obtained by uniformly mixing predetermined amounts of the first to third components described above, but this mixing is preferably carried out at 50 to 100°C, for example at 100°C. The desired homogeneous gel composition can be obtained by uniformly dissolving the aforementioned fatty acid ester or aliphatic hydrocarbon and dextrin fatty ester in silicone oil by heating and stirring, and then cooling.
なお、この組成物に各種の油性剤、香料、医薬用成分、
酸化防止剤、顔料、染料などを添加することは本発明の
組成物の物性に大きな変更を来たさない範囲であれば任
意とされる。In addition, this composition contains various oily agents, fragrances, pharmaceutical ingredients,
Addition of antioxidants, pigments, dyes, etc. is optional as long as it does not significantly change the physical properties of the composition of the present invention.
つぎに本発明の実施例をあげるが1例中の部は重量部を
、また粘度は25℃での測定値を示したものである。Next, examples of the present invention will be given, in which parts are parts by weight, and viscosity is a value measured at 25°C.
実施例1〜10
第1表に示した量のオクタメチルシクロテトラシロキサ
ン・KF994 (信越化学工業■製部品名〕およびデ
カメチルシクロペンタシロキサンKF995 [同社製
商品名]に第1表で示した種類および量の高級脂肪酸エ
ステルまたは脂肪族炭化水素ならびに第1表に示した量
のデキストリン脂肪酸エステルを添加し、この総量30
0gを500+nflの硬質ガラスフラスコ中に投入し
、60〜70℃で攪拌して均一溶液となったことを確認
して攪拌を停止し、氷水浴で急冷したところ、均一なゲ
ル状組成物が得られたので、この組成物についての稠度
、離油度をJIS K2220に準拠した方法で測定
したところ第1表に併記したとうりの結果が得られた。Examples 1 to 10 Octamethylcyclotetrasiloxane KF994 (product name manufactured by Shin-Etsu Chemical Co., Ltd.) and decamethylcyclopentasiloxane KF995 [product name manufactured by the same company] in the amounts shown in Table 1 were added to the types shown in Table 1. and the amount of higher fatty acid ester or aliphatic hydrocarbon and the amount of dextrin fatty acid ester shown in Table 1, and the total amount of 30
0g was put into a 500+nfl hard glass flask, stirred at 60-70°C, and after confirming that it had become a homogeneous solution, stirring was stopped and quenched in an ice water bath, a homogeneous gel-like composition was obtained. Therefore, the consistency and oil separation of this composition were measured according to JIS K2220, and the results shown in Table 1 were obtained.
比較例
実施例で使用した環状ジメチルポリシロキサン・KF9
94またはKF995 270部に、デキストリン脂肪
エステル・レオパールKL(千葉製粉■製部品名)30
部を添加し、500m12の硬化ガラスフラスコ中で6
0〜70 ’Cに攪拌したが、レオパールKLはシリコ
ーンオイルに均一に溶解せず、攪拌後に氷水浴で急冷し
たものはレオパールKLが沈殿となり、全くゲル化は認
められなかった・
:L’:”、f、’
手続補正書
昭和61年5月12日
特許庁長官 宇 賀 道 部 殿 −′−“。Comparative Example Cyclic dimethylpolysiloxane KF9 used in Example
94 or 270 parts of KF995, 30 parts of dextrin fatty ester Leopard KL (part name manufactured by Chiba Flour Milling)
6 parts in a 500 m12 hardened glass flask.
Although it was stirred at 0 to 70'C, Leopard KL did not dissolve uniformly in the silicone oil, and when it was rapidly cooled in an ice water bath after stirring, Leopard KL precipitated and no gelation was observed. ”,f,' Procedural Amendment May 12, 1986 Mr. Michibu Uga, Commissioner of the Patent Office -'-“.
1、事件の表示
昭和60年特許願第284930号
2、発明の名称
ゲル状組成物
3、補正をする者
事件との関係 特許出願人
名称 (206)信越化学工業株式会社4、代理人
・ 1
−・−・1
5、補正命令の日付
「自発」
6、補正の対象
明細書の「発明の詳細な説明の欄」
■)明細書第9頁第1行の「肪酸エステル」を「肪酸エ
ステル・レオパールKL[千葉製粉■製部品名〕」と補
正する。1. Indication of the case 1985 Patent Application No. 284930 2. Name of the invention Gel composition 3. Person making the amendment Relationship to the case Name of patent applicant (206) Shin-Etsu Chemical Co., Ltd. 4. Agent 1. -・-・1 5. Date of amendment order “voluntary” 6. “Detailed description of the invention column” of the specification subject to amendment ■) “Fatty acid ester” in the first line of page 9 of the specification Acid ester Leopard KL [Part name manufactured by Chiba Flour Mills]".
2)明細書第10頁第1表の欄外(註)1)および(註
)4)における「〔日清精油@裂開品名〕」を「〔日清
製油■装面品名〕」と補正する。2) In the margins (notes) 1) and (notes) 4) of Table 1 on page 10 of the specification, "[Nissin essential oil @ split product name]" is amended to "[Nissin oil ■ mounting product name]" .
以上that's all
Claims (1)
ルコールとのエステルまたは炭素数10〜40の脂肪族
炭化水素から選ばれる1種または2種以上の混合物5〜
50重量部、 3)デキストリン脂肪酸エステル 5〜30重量部 とからなることを特徴とするゲル状組成物。[Claims] 1, 1) 30 to 90 parts by weight of a cyclic dimethylpolysiloxane represented by the formula ▲ Numerical formula, chemical formula, table, etc. ▼ (n = 3 to 6), 2) Fatty acid having 8 to 24 carbon atoms and a C1-C24 aliphatic alcohol or a mixture of one or more selected from C10-40 aliphatic hydrocarbons5-
3) 5 to 30 parts by weight of dextrin fatty acid ester.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP28493085A JPS62143971A (en) | 1985-12-17 | 1985-12-17 | Gelatinous composition |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP28493085A JPS62143971A (en) | 1985-12-17 | 1985-12-17 | Gelatinous composition |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS62143971A true JPS62143971A (en) | 1987-06-27 |
JPH036180B2 JPH036180B2 (en) | 1991-01-29 |
Family
ID=17684897
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP28493085A Granted JPS62143971A (en) | 1985-12-17 | 1985-12-17 | Gelatinous composition |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS62143971A (en) |
Cited By (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS63216817A (en) * | 1987-03-06 | 1988-09-09 | Terumo Corp | Gelatinous composition |
JPH0368505A (en) * | 1989-08-09 | 1991-03-25 | Kao Corp | Oily lotion for external application |
US5236986A (en) * | 1991-02-27 | 1993-08-17 | Shin-Etsu Chemical Co., Ltd. | Silicone polymers and water-dispersable, pasty silicone oil compositions comprising the same |
US5919437A (en) * | 1996-05-24 | 1999-07-06 | Colgate-Palmolive Company | Cosmetic cream composition containing silicone gel material |
JP2002193747A (en) * | 2000-12-28 | 2002-07-10 | Kose Corp | Oily makeup cosmetic |
EP1935924A1 (en) | 2002-09-12 | 2008-06-25 | Shin-Etsu Chemical Company, Ltd. | Novel organopolysiloxane polymer, pasty composition, and cosmetic preparation containing the same |
EP2898924A1 (en) | 2014-01-23 | 2015-07-29 | Shin-Etsu Chemical Co., Ltd. | Cosmetic composition containing two crosslinking organopolysiloxane polymers |
JP2016065956A (en) * | 2014-09-24 | 2016-04-28 | 富士ゼロックス株式会社 | Electrophotographic photoreceptor, process cartridge, and image forming apparatus |
KR20160110125A (en) | 2015-03-13 | 2016-09-21 | 신에쓰 가가꾸 고교 가부시끼가이샤 | Gel paste composition and cosmetic using the gel paste composition |
WO2023063032A1 (en) | 2021-10-12 | 2023-04-20 | 信越化学工業株式会社 | Organoalkoxysilane-containing composition, method for producing same and water absorption inhibitor |
-
1985
- 1985-12-17 JP JP28493085A patent/JPS62143971A/en active Granted
Cited By (16)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS63216817A (en) * | 1987-03-06 | 1988-09-09 | Terumo Corp | Gelatinous composition |
JPH0368505A (en) * | 1989-08-09 | 1991-03-25 | Kao Corp | Oily lotion for external application |
US5236986A (en) * | 1991-02-27 | 1993-08-17 | Shin-Etsu Chemical Co., Ltd. | Silicone polymers and water-dispersable, pasty silicone oil compositions comprising the same |
US5919437A (en) * | 1996-05-24 | 1999-07-06 | Colgate-Palmolive Company | Cosmetic cream composition containing silicone gel material |
JP2002193747A (en) * | 2000-12-28 | 2002-07-10 | Kose Corp | Oily makeup cosmetic |
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EP2898924A1 (en) | 2014-01-23 | 2015-07-29 | Shin-Etsu Chemical Co., Ltd. | Cosmetic composition containing two crosslinking organopolysiloxane polymers |
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US11020327B2 (en) | 2015-03-13 | 2021-06-01 | Shin-Etsu Chemical Co., Ltd. | Gel paste composition and cosmetic using the gel paste composition |
WO2023063032A1 (en) | 2021-10-12 | 2023-04-20 | 信越化学工業株式会社 | Organoalkoxysilane-containing composition, method for producing same and water absorption inhibitor |
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