JPH086035B2 - Silicone gel composition and cosmetics containing the same - Google Patents
Silicone gel composition and cosmetics containing the sameInfo
- Publication number
- JPH086035B2 JPH086035B2 JP63015442A JP1544288A JPH086035B2 JP H086035 B2 JPH086035 B2 JP H086035B2 JP 63015442 A JP63015442 A JP 63015442A JP 1544288 A JP1544288 A JP 1544288A JP H086035 B2 JPH086035 B2 JP H086035B2
- Authority
- JP
- Japan
- Prior art keywords
- silicone
- gel composition
- viscosity
- weight
- benzene
- 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
Classifications
-
- 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
- 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
- A61K8/72—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
- 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
- A61K2800/59—Mixtures
- A61K2800/594—Mixtures of polymers
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)
- Dermatology (AREA)
- Chemical & Material Sciences (AREA)
- Dispersion Chemistry (AREA)
- Cosmetics (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Description
【発明の詳細な説明】 [産業上の利用分野] 本発明は、特定のシリコーン重合物と低粘度シリコー
ン油とからなるシリコーンゲル組成物並びにこれを含有
する化粧料に関するもので、更に詳しくはソフトで安定
性に優れた、特に化粧品用素材として有用なシリコーン
ゲル組成物並びにこれを含有せしめることにより、なめ
らかでさっぱりした感触を有する使用感、使用性、そし
て経時安定性に優れた安全性の高い化粧料の提供を目的
とするものである。TECHNICAL FIELD The present invention relates to a silicone gel composition comprising a specific silicone polymer and a low-viscosity silicone oil, and a cosmetic containing the same, more specifically, a soft gel composition. And highly stable silicone gel composition, which is particularly useful as a cosmetic material, and by containing it, it has a smooth and refreshing feel, excellent usability, usability, and stability over time, and high safety. The purpose is to provide cosmetics.
[従来の技術] 従来、シリコーン油は、その優れた特性から様々な製
品に応用されており、特に化粧料関係においても有用な
油剤成分として汎用されている。このことはシリコーン
油がべたつきが少なくなめらかで伸びがよく、さっぱり
した感触を持ち、また潤滑性、撥水性に富むとともに無
味・無臭で皮膚安全性が高い等の好適な特徴ないし条件
を具備しているためである。従ってシリコーン油を配
合、活用することで良好な使用感を有し、皮膚・毛髪を
トリートメントし保護する基礎化粧料や頭髪化粧料、あ
るいは化粧持続性の良好なメーキャップ化粧料の製品化
検討がなされてきた。[Prior Art] Conventionally, silicone oil has been applied to various products due to its excellent properties, and is generally used as a useful oil agent component particularly in cosmetics. This means that the silicone oil has suitable characteristics or conditions such as low stickiness, smoothness, good elongation, a refreshing feel, rich lubricity and water repellency, tasteless and odorless, and high skin safety. This is because Therefore, it is considered to commercialize basic cosmetics and hair cosmetics that have a good feeling of use by blending and utilizing silicone oil and treat and protect the skin and hair, or makeup cosmetics with good makeup lasting. Came.
通常、係る化粧品用シリコーン油としては分子量、粘
度の相違する鎖状のジメチルポリシロキサンを代表に、
環状のオクタメチルシクロテトラシロキサン、デカメチ
ルシクロペンタシロキサン、またメチルフェニルポリシ
ロキサン、メチルハイドロジェンポリシロキサンが挙げ
られ、その他各種の重合・共重合体物、変性物が市販さ
れている。In general, such cosmetic silicone oils are represented by chain-like dimethylpolysiloxanes having different molecular weights and viscosities,
Examples thereof include cyclic octamethylcyclotetrasiloxane, decamethylcyclopentasiloxane, methylphenylpolysiloxane, and methylhydrogenpolysiloxane, and various other polymerization / copolymer products and modified products are commercially available.
これら各種シリコーン油は化粧目的、期待すべき効果
を考慮して使いわけや併用が行なわれている。例えば低
粘度ジメチルポリシロキサンはべたつきが少なくさっぱ
りした感触が求められる製品に、また一層高粘度のもの
は水を効果的にはじく撥水性を有する製品に適用され、
さらに鎖状、環状の揮発性シリコーン油は塗布後揮散し
てしまう性質があるので清涼感を必要とする製品等に用
いられることが多い。そしてまたジメチルハイドロジェ
ンポリシロキサンは化粧用粉体の疎水化処理に利用する
ことでメーキャップ化粧料の化粧もちの向上が図られて
きた。These various silicone oils are used or used in combination in consideration of cosmetic purposes and expected effects. For example, low-viscosity dimethylpolysiloxane is applied to products that are required to have a refreshing feel with little stickiness, and higher-viscosity dimethylpolysiloxane is applied to products that have water repellency that effectively repels water,
Furthermore, since chain-like and cyclic volatile silicone oils have the property of volatilizing after application, they are often used for products requiring a refreshing feeling. Further, dimethylhydrogenpolysiloxane has been used to improve the makeup lasting property of makeup cosmetics by utilizing it for the hydrophobic treatment of cosmetic powders.
一般にこうしたシリコーン油の特性を有効に活用した
技術が知られるとともに化粧料への用途開発研究の努力
も行なわれてきた。In general, techniques for effectively utilizing such characteristics of silicone oil have been known, and efforts have been made to research and develop applications for cosmetics.
[発明が解決しようとする課題] 前記した如く、シリコーン油は化粧品用油剤として重
要であるものの、一層機能性を高めた期待する製品を得
る上で以下に述べるように不都合がしばしば見受けら
れ、指摘されるところであった。[Problems to be Solved by the Invention] As described above, although silicone oil is important as an oil agent for cosmetics, there are often inconveniences as described below in obtaining expected products having higher functionality, It was about to be done.
シリコーン油は、概して他の化粧品用油剤との相溶性
が悪く、均一溶解し安定したシリコーン油をベースとす
る製品の調製が困難であった。シリコーン油を配合する
場合、乳化しエマルジョンにして、またワックスその他
の化粧品油剤と混合して行なっても安定に維持し難く、
時にシリコーン油の特性を効果的に発揮させるべく多量
に含有せしめると経時的に分離現象を招くことがあっ
た。このことは特にさっぱりした感触を付与することや
メーキャップ化粧料の化粧もちを高めるめに低粘度もし
くは揮発性シリコーン油を多用した時に顕著に認められ
ることであった。そして高粘度シリコーン油を使用する
場合には撥水性は向上するがべたつき感等も同時に感じ
られる結果になる。このようなシリコーン油の含有量を
増加させ、充分に効果を期待し、しかも安定した製品を
得る上で苦心を強いられた。Silicone oils generally have poor compatibility with other cosmetic oils, making it difficult to prepare a product based on a homogeneously dissolved and stable silicone oil. When silicone oil is blended, it is difficult to maintain it stable even when emulsified to form an emulsion and mixed with wax and other cosmetic oils.
At times, if a large amount is contained in order to effectively exhibit the characteristics of the silicone oil, a separation phenomenon may occur over time. This was particularly noticeable when a low-viscosity or volatile silicone oil was used in a large amount in order to impart a refreshing feel and to enhance the makeup lasting property of makeup cosmetics. When a high-viscosity silicone oil is used, the water repellency is improved, but a sticky feeling or the like is simultaneously felt. It has been difficult to increase the content of such silicone oil, expect a sufficient effect, and obtain a stable product.
また従来のシリコーン油では流動特性として降伏値を
持たないため、化粧料の主骨格として使用する場合、例
えば顔料などの比重差のある物質を経時的に安定分散さ
せることが難しい。In addition, since conventional silicone oils do not have a yield value as a flow characteristic, when used as the main skeleton of cosmetics, it is difficult to stably disperse substances having a specific gravity difference such as pigment over time.
係る点から分子量の大きい高粘度のものを使用したと
しても、比重差の大きいものを保持できず、沈降等が見
られるとともに上述した如く、べたつき感が生じ、感触
上好ましくない。一方、ワックス類と併用した場合に
は、相溶性も悪くワックスの析出が起こり易くなるとと
もにワックス自身の性質が現われ、化粧料ベースとして
シリコーン油の特長であるなめらかでさっぱりした感触
を損うこととなり、シリコーン油の特性を充分に活かし
た安定性の良い製品を得ることが困難であった。すなわ
ちシリコーン油は従来液体油剤としての利用が一般的で
あり、構造維持性のある製品が強く要望されているにも
かかわらず、これに応えた充分満足した製品が調製し難
い面を有していた。From this point of view, even if a high-viscosity product having a large molecular weight is used, a product having a large difference in specific gravity cannot be retained, sedimentation and the like are observed, and as described above, a sticky feeling occurs, which is not preferable in terms of feel. On the other hand, when used in combination with waxes, the compatibility is poor and the wax is likely to precipitate, and the properties of the wax itself appear. However, it has been difficult to obtain a product with good stability that fully utilizes the characteristics of silicone oil. That is, silicone oils have conventionally been generally used as liquid oil agents, and despite the strong demand for products having a structure-maintaining property, it is difficult to prepare products that meet this requirement and that are sufficiently satisfactory. Was.
[課題を解決するための手段] 本発明者等は、前記した事情に鑑み、鋭意研究した結
果、ベンゼンに不溶であるが、同重量以上のベンゼンを
含みうる三次元架橋の構造を有するシリコーン重合物と
低粘度シリコーン油を混和することにより、ソフトで安
定性の優れたシリコーンゲル組成物が得られることを見
い出し、さらには前記シリコーンゲル組成物を含有せし
めることにより、安定性がよくなめらかでさっぱりした
感触を有する使用感、使用性に優れた化粧料が得られる
ことを見い出し、これら知見をもって本発明を完成させ
たのである。[Means for Solving the Problems] The inventors of the present invention have conducted intensive studies in view of the above-mentioned circumstances, and as a result, have found that the silicone polymerization is insoluble in benzene but has a three-dimensional crosslinked structure that can contain benzene in the same amount or more. It was found that a soft and excellent silicone gel composition can be obtained by mixing a silicone oil composition and a low-viscosity silicone oil. Furthermore, by incorporating the silicone gel composition, stability and smoothness and refreshing are obtained. It was found that a cosmetic having excellent feeling in use and usability can be obtained, and the present invention has been completed based on these findings.
すなわち本発明は、ベンゼンに不溶であるが、自重と
同重量以上のベンゼンを含みうる、R2SiO単位とRSiO1.5
単位の比率が1〜30:1である三次元架橋構造を有するシ
リコーン重合物と、50cs以下の低粘度シリコーン油とか
らなり、かつ、シリコーン重合物と低粘度シリコーン油
との重量比率が5:95〜30:70であることを特徴とするシ
リコーンゲル組成物、並びに、前記シリコーンゲル組成
物を含有する化粧料に関するものである。That is, the present invention is insoluble in benzene, but may contain the same weight or more of benzene as its own weight, R 2 SiO units and R SiO 1.5
A silicone polymer having a three-dimensional crosslinked structure having a unit ratio of 1 to 30: 1 and a low-viscosity silicone oil of 50 cs or less, and the weight ratio of the silicone polymer to the low-viscosity silicone oil is 5: The present invention relates to a silicone gel composition characterized by being 95 to 30:70, and a cosmetic containing the silicone gel composition.
以下本発明の構成について説明する。 The configuration of the present invention will be described below.
本発明のシリコーンゲル組成物は、ベンゼンに不溶で
あるが、自重と同重量以上のベンゼンを含みうる三次元
架橋構造を有するシリコーン重合物と低粘度シリコーン
油とからなるもので、シリコーン重合構造物に低粘度シ
リコーン油が混和されている。The silicone gel composition of the present invention comprises a silicone polymer having a three-dimensional crosslinked structure which is insoluble in benzene but can contain benzene in an amount equal to or more than its own weight, and a low-viscosity silicone oil. Low viscosity silicone oil is mixed in.
係るベンゼンに不溶で、自重と同重量以上のベンゼン
を含みうる三次元架橋構造を有するシリコーン重合物
は、オルガノポリシロキサンを架橋結合させて得られる
重合物であり、一部に三次元架橋構造を有し、R2SiO単
位及びRSiO1.5単位よりなり、R3SiO0.5単位及び/又はS
iO2単位を含んでいても良い。Such a silicone polymer having a three-dimensional crosslinked structure which is insoluble in benzene and may contain benzene in the same weight as or more than its own weight is a polymer obtained by cross-linking an organopolysiloxane, and partially has a three-dimensional crosslinked structure. Having R 2 SiO units and R SiO 1.5 units, R 3 SiO 0.5 units and / or S
It may contain iO 2 units.
前記した各構成単位のRは水素原子、メチル基、エチ
ル基、プロピル基等のアルキル基、フェニル基、トリル
基等などのアリール基、およびビニル基等の脂肪族不飽
和基などが例示され、同種又は異なった種類であっても
良い。Examples of R of each structural unit described above include a hydrogen atom, an alkyl group such as a methyl group, an ethyl group and a propyl group, an aryl group such as a phenyl group and a tolyl group, and an aliphatic unsaturated group such as a vinyl group. The same kind or different kinds may be used.
オルガノポリシロキサンが、ベンゼンに不溶である
が、自重と同重量以上のベンゼンを含みうる三次元架橋
構造を有するシリコーン重合構造を取るためには、RSiO
1.5単位及びSiO2単位と、R2SiO単位及びR3SiO0.5単位と
の比が適当な範囲にあることが必要で、RSiO1.5単位及
びSiO2単位の比率が小さくなるとオルガノポリシロキサ
ンは十分な三次元架橋構造とならず、ベンゼンに可溶と
なり、たとえ見掛上架橋構造をとっても本発明には使用
できない。Organopolysiloxane is insoluble in benzene, but in order to have a silicone polymerized structure having a three-dimensional crosslinked structure that can contain benzene in an amount equal to or more than its own weight, RSiO is used.
It is necessary that the ratio of 1.5 units and SiO 2 units to R 2 SiO units and R 3 SiO 0.5 units is in an appropriate range. If the ratio of R SiO 1.5 units and SiO 2 units becomes small, the organopolysiloxane will be sufficient. It does not have a three-dimensional crosslinked structure and is soluble in benzene, and even if it has an apparent crosslinked structure, it cannot be used in the present invention.
また、R2SiO単位及びR3SiO0.5単位に比して、RSiO1.5
単位及びSiO2単位が多すぎるとオルガノポリシロキサン
は強固な架橋構造をとり、ベンゼンは不溶ではあるが、
重合物の自重量未満しかベンゼンを含まず、これは、低
粘度シリコーン油と混和すると分離、排出を生じてしま
い本発明には使用できなくなる。In addition, in comparison with R 2 SiO unit and R 3 SiO 0.5 unit, RSiO 1.5
If there are too many units and SiO 2 units, the organopolysiloxane has a strong cross-linked structure and benzene is insoluble,
The polymer contains benzene in an amount less than its own weight, and when mixed with a low-viscosity silicone oil, it causes separation and discharge, and cannot be used in the present invention.
本発明に使用されるベンゼンに不溶な、自重と同重量
以上のベンゼンを含みうるシリコーン重合物におけるR2
SiO単位とRSiO1.5単位の比率は、シリコーン重合物全体
の分子量による影響も大きく厳密には規定し難いが、1
〜30:1の割合であるものが本発明の実施に望ましい結果
を与えた。RSiO1.5単位がこの比よりも多くなると硬い
シリコーン重合物となり、自重と同重量未満のベンゼン
しか含み得ず、このものは後述する低粘度シリコーン油
での混和の際シリコーン重合物が充分に膨潤せず、シリ
コーン油の分離、排出がおこり、安定維持ができなくな
るようになる。逆にR2SiO単位が上記範囲を超えると構
造粘性が乏しくなり、本発明の特長を示さなくなってし
まう。このため、ソフトで安定性の良好なシリコーンゲ
ル組成物を得る本発明の目的にとって、前記した構造単
位の割合にあることが必要である。R 2 in the silicone polymer used in the present invention, which is insoluble in benzene and may contain benzene in an amount equal to or more than its own weight
The ratio of the SiO unit to the RSiO 1.5 unit is largely influenced by the molecular weight of the entire silicone polymer, and it is difficult to strictly define it, but 1
A ratio of ~ 30: 1 gave desirable results in the practice of the invention. When the RSiO 1.5 unit is more than this ratio, it becomes a hard silicone polymer and can contain less than the same weight of benzene as its own weight, and this silicone polymer swells sufficiently when mixed with a low viscosity silicone oil described later. Instead, the silicone oil will be separated and discharged, making it impossible to maintain stability. On the contrary, when the R 2 SiO unit exceeds the above range, the structural viscosity becomes poor and the features of the present invention are not exhibited. Therefore, for the purpose of the present invention to obtain a silicone gel composition which is soft and has good stability, it is necessary that the ratio of the structural units is within the above range.
本発明のベンゼンに不溶であるが、自重と同重量以上
のベンゼンを含みうる三次元架橋構造を有するシリコー
ン重合物は、種々の方法で合成することができる。The silicone polymer of the present invention, which is insoluble in benzene but has a three-dimensional crosslinked structure which can contain benzene in an amount equal to or more than its own weight, can be synthesized by various methods.
1分子中に少なくとも2個のケイ素原子に結合した水
素原子を有するオルガノハイドロジェンポリシロキサン
に触媒量のアルカリ金属水酸化物のアルコール性水溶液
を加え加熱して脱水素反応及び縮合反応を行なうことも
一方法である。It is also possible to carry out a dehydrogenation reaction and a condensation reaction by adding a catalytic amount of an alcoholic aqueous solution of an alkali metal hydroxide to an organohydrogenpolysiloxane having at least two hydrogen atoms bonded to silicon atoms in one molecule and heating it. One way.
一方の分子に少なくとも2個のケイ素原子に結合した
水素原子を有するオルガノハイドロジェンポリシロキサ
ンに他方の分子に少なくとも2個のケイ素原子に結合し
た水酸基を有するオルガノポリシロキサンを触媒量のア
ルカリ金属水酸化物や白金化合物等の存在化に加熱し、
脱水素縮合反応を行なうことも一方法である。A catalytic amount of an organohydrogenpolysiloxane having a hydrogen atom bonded to at least two silicon atoms in one molecule and an organopolysiloxane having a hydroxyl group bonded to at least two silicon atoms in the other molecule in a catalytic amount Heated to the presence of things and platinum compounds,
One method is to carry out a dehydrogenative condensation reaction.
1分子中に少なくとも2個のケイ素原子に直結した水
酸基を有するオルガノポリシロキサンを触媒量のアルカ
リ金属水酸化物や有機錫化合物の存在下に加熱し脱水縮
合反応を行なうことも一方法である。One method is to heat the organopolysiloxane having a hydroxyl group directly bonded to at least two silicon atoms in one molecule in the presence of a catalytic amount of an alkali metal hydroxide or an organic tin compound to carry out the dehydration condensation reaction.
1分子中に少なくとも2個のケイ素原子に直結した水
酸基を有するオルガノポリシロキサンと、他方の分子に
少なくとも2個のケイ素原子に結合したアルコキシ基を
有するオルガノポリシロキサンを触媒量のアルカリ金属
水酸化物や有機金属錫化合物の存在下に加熱して脱アル
コール反応を行なうことも一方法で、いずれの方法にて
も本発明のベンゼンに不溶であるが、自重と同重量以上
のベンゼンを含み得る三次元架橋構造を有するシリコー
ン重合物を容易に得ることができる。A catalytic amount of an alkali metal hydroxide having an organopolysiloxane having a hydroxyl group directly bonded to at least two silicon atoms in one molecule and an organopolysiloxane having an alkoxy group bonded to at least two silicon atoms in the other molecule. It is also one method to carry out dealcoholization reaction by heating in the presence of or an organometallic tin compound, and any method is insoluble in benzene of the present invention, but can contain benzene in the same weight or more as its own weight. A silicone polymer having an original crosslinked structure can be easily obtained.
一方、本発明に用いられる低粘度シリコーン油は、粘
度50cs以下のものが好適に使用し得る。これは高粘度に
なるにつれ、それを多量に用いた結果として感触的にあ
ぶらっぽさが生じ、使用感上好ましくない方法となるか
らである。そして低粘度シリコーン油としては低重合度
鎖状のジメチルポリシロキサン、メチルフェニルポリシ
ロキサン、環状のオクタメチルシクロテトラシロキサ
ン、デカメチルシクロペンタシロキサン等が例示され、
必要に応じてこれらの1種または2種以上を適宜選択し
て用いられる。On the other hand, as the low-viscosity silicone oil used in the present invention, those having a viscosity of 50 cs or less can be suitably used. This is because, as the viscosity increases, a large amount of it is used, resulting in a feeling of oiliness, which is not preferable in terms of usability. Examples of the low-viscosity silicone oil include low-polymerization degree chain dimethylpolysiloxane, methylphenylpolysiloxane, cyclic octamethylcyclotetrasiloxane, and decamethylcyclopentasiloxane.
One or more of these may be appropriately selected and used as needed.
本発明のシリコーンゲル組成物は、前記の如くして得
たシリコーン重合物と低粘度シリコーン油とを充分混練
等し、膨潤させることで容易に調製することができる。
この場合、シリコーン重合物と低粘度シリコーン油との
混合割合は重量比で5対95〜30対70、好ましくは10対90
〜25対75である。シリコーン重合物の量が少なくなると
低粘度シリコーン油が過剰となって、流動粘性を帯び良
好なゲル構造を維持できなくなり、逆に多くなると軟ら
かいゲル組成物が得難くなるからである。The silicone gel composition of the present invention can be easily prepared by sufficiently kneading the silicone polymer obtained as described above and a low-viscosity silicone oil and swelling them.
In this case, the mixing ratio of the silicone polymer and the low-viscosity silicone oil is 5:95 to 30:70 by weight, preferably 10:90.
~ 25 to 75. This is because when the amount of the silicone polymer is small, the low-viscosity silicone oil becomes excessive, and it becomes impossible to maintain a good gel structure with flow viscosity, and when the amount is large, it becomes difficult to obtain a soft gel composition.
前述の本発明によって得られたシリコーンゲル組成物
は、安定性がよく、ソフトでさっぱりとした感触を有す
る使用感、使用性に優れたものである。このシリコーン
ゲル組成物を従来シリコーン油と同様に化粧品用原料と
して利用することでその特性が発揮された極めて有用な
化粧料が得られる。The above-mentioned silicone gel composition obtained by the present invention is excellent in stability, soft and refreshing feeling, and is excellent in usability and usability. By using this silicone gel composition as a raw material for cosmetics in the same manner as conventional silicone oils, extremely useful cosmetics exhibiting its properties can be obtained.
本発明での化粧料としては、クリーム・乳液等の顔、
手足用の基礎化粧料、整髪料・シャンプー・リンス等の
頭髪化粧料、ファンデーション・白粉・頬紅・アイシャ
ドウ・口紅・美爪料等のメーキャップ化粧料であり、こ
れは本発明のシリコーンゲル組成物が適用しうるもので
あれば何れを問うものでない。そしてシリコーンゲル組
成物の配合はエマルションにして、また他の油剤原料と
同様に混合して添加することで行なわれる。この際、配
合量は5〜100重量%の範囲であり、そのまま用いても
よく使用目的に応じて決定すればよい。As the cosmetics in the present invention, a face such as cream / milky lotion,
Basic cosmetics for limbs, hair cosmetics such as hair styling, shampoo, and rinse, makeup cosmetics such as foundation, white powder, blush, eyeshadow, lipstick, and beautiful nails, which are the silicone gel composition of the present invention. It does not matter which one is applicable. The silicone gel composition is blended in the form of an emulsion and mixed and added in the same manner as the other oil agent raw materials. In this case, the compounding amount is in the range of 5 to 100% by weight, and it may be used as it is or may be determined according to the purpose of use.
なお、本発明に於ける化粧料は当然のことながら前記
シリコーンゲル組成物と従来化粧料基材となる成分とか
ら構成される。化粧料基材成分をより具体的に例示すれ
ば、油脂類・ロウ類・炭化水素類・脂肪酸・高級アルコ
ール・エステル類・金属石ケン・シリコーン油等の油剤
原料、白色顔料・着色顔料・体質顔料等の粉体原料、界
面活性剤、多価アルコール類、高分子化合物、水、その
他防腐剤、アルカリ剤、紫外線吸収剤、酸化防止剤、タ
ール色素、美肌用成分等であり、これらは製品種や化粧
目的に応じて適宜選択される。The cosmetic in the present invention is naturally composed of the above-mentioned silicone gel composition and a conventional cosmetic base material. More concrete examples of the base material for cosmetics include oils, waxes, hydrocarbons, fatty acids, higher alcohols, esters, metal soap, silicone oil, and other raw materials for oil agents, white pigments, colored pigments, and constitutions. Powder raw materials such as pigments, surfactants, polyhydric alcohols, polymer compounds, water and other preservatives, alkali agents, ultraviolet absorbers, antioxidants, tar dyes, skin-care ingredients, etc. It is appropriately selected depending on the seed and the purpose of makeup.
[実施例] 以下、本発明について実施例を挙げてさらに説明す
る。なお、これらは本発明を何ら限定するものでない。[Examples] Hereinafter, the present invention will be further described with reference to examples. These do not limit the present invention at all.
実施例[1] トリメチルシリル末端封鎖ジメチルメチルハイドロジ
ェンポリシロキサン《分子量2300、CH3HSiO対(CH3)2SiO
=1対4(モル比)》に1%水酸化カリウム溶液(エタ
ノール対水=2対1)を適量加え、加熱、還流して重合
反応を行ない、反応生成物を得た。次いでこの反応生成
物を水洗浄してアルカリ剤を除去後、自然乾燥させるこ
とによりベンゼンに不溶であり、ベンゼンを自重の180
%含み得るシリコーン重合物を製造した。Example [1] trimethylsilyl endblocked dimethyl methylhydrogen polysiloxane "molecular weight 2300, CH 3 HSiO pairs (CH 3) 2 SiO
= 1: 4 (molar ratio) >>, an appropriate amount of a 1% potassium hydroxide solution (ethanol: water = 2: 1) was added, heated and refluxed to carry out a polymerization reaction to obtain a reaction product. Then, this reaction product is washed with water to remove the alkaline agent, and then naturally dried to be insoluble in benzene and
% Silicone polymer was prepared.
このシリコーン重合物2重量部とジメチルポリシロキ
サン(粘度5cs)8重量部とを分散混合後、三本ロール
により充分混練し、膨潤させてシリコーンゲル組成物を
調製した。2 parts by weight of this silicone polymer and 8 parts by weight of dimethylpolysiloxane (viscosity 5 cs) were dispersed and mixed, and then sufficiently kneaded with a three-roll and swollen to prepare a silicone gel composition.
実施例[2] トリメチルシリル末端封鎖ジメチルメチルハイドロジ
ェンポリシロキサン《分子量4800、CH3HSiO対(CH3)2SiO
=3対9.6(モル比)》を用いた以外は実施例[1]と
同様に操作して、シリコーン重合物を製造した。Example [2] trimethylsilyl endblocked dimethyl methylhydrogen polysiloxane "molecular weight 4800, CH 3 HSiO pairs (CH 3) 2 SiO
= 3: 9.6 (molar ratio) >> was used, and a silicone polymer was produced in the same manner as in Example [1].
得られたシリコーン重合物は、ベンゼンに不溶であ
り、ベンゼンを自重の130%含み得るものであった。The obtained silicone polymer was insoluble in benzene and could contain benzene at 130% of its own weight.
このシリコーン重合物2重量部とジメチルポリシロキ
サン(粘度5cs)8重量部とを分散混合後、三本ロール
により充分に混練し、膨潤させてシリコーンゲル組成物
を調製した。2 parts by weight of this silicone polymer and 8 parts by weight of dimethylpolysiloxane (viscosity 5 cs) were dispersed and mixed, and then sufficiently kneaded by a three-roll and swollen to prepare a silicone gel composition.
比較例[1] トリメチルシリル末端封鎖ジメチルメチルハイドロジ
ェンポリシロキサン《分子量2200、CH3HSiO対(CH3)2SiO
=3対2.6(モル比)》を用いた以外は実施例[1]と
同様に操作して、シリコーン重合物を製造した。Comparative Example [1] trimethylsilyl endblocked dimethyl methylhydrogen polysiloxane "molecular weight 2200, CH 3 HSiO pairs (CH 3) 2 SiO
= 3: 2.6 (molar ratio) >> was used and a silicone polymer was produced in the same manner as in Example [1].
得られたシリコーン重合物は自重の60%のベンゼンし
か含み得ない比較的硬く、脆いシリコーン重合物であっ
た。このシリコーン重合物を用いて実施例[1]と同様
にしてシリコーンゲル組成物を調製した。The obtained silicone polymer was a relatively hard and brittle silicone polymer which could contain only 60% by weight of benzene. Using this silicone polymer, a silicone gel composition was prepared in the same manner as in Example [1].
以上の如くして作成した本発明の実施例[1]及び
[2]のシリコーンゲル組成物は軟らかなゲルであり、
伸びがよくさっぱりした感触を有し、経時安定性にも優
れたものであった。The silicone gel compositions of Examples [1] and [2] of the present invention prepared as described above are soft gels,
It had good elongation, a refreshing feel, and excellent stability over time.
これに対して比較例[1]にあっては、そこで得られ
たシリコーンゲルが硬く、しかもこのものと低粘度シリ
コーン油との混和性が悪く、廃液現象が起こり、安定性
の良好なゲル組成物を調製することができなかった。On the other hand, in Comparative Example [1], the silicone gel obtained there was hard, and the miscibility of the silicone gel with low-viscosity silicone oil was poor. The product could not be prepared.
次に、本発明で得たシリコーンゲル組成物を用いた化
粧料の例を示す。Next, examples of cosmetics using the silicone gel composition obtained in the present invention will be shown.
実施例[3] ファンデーション (処方) (重量部) 1.酸化チタン 14.0 2.マイカ 3.0 3.着色顔料 3.0 4.実施例[1]のシリコーンゲル組成物 80.0 (製法) 成分1〜3を混合、粉砕して均一にし、これを成分4
に添加混合し、均質分散した後、容器に充填して製品を
得た。Example [3] Foundation (prescription) (parts by weight) 1. Titanium oxide 14.0 2. Mica 3.0 3. Color pigment 3.0 4. Silicone gel composition 80.0 of Example [1] (production method) Mix components 1 to 3, Grind to homogeneity and add this to ingredient 4
Was added to and mixed with, and homogeneously dispersed, and then filled in a container to obtain a product.
比較例[2] ファンデーション 実施例[3]の成分4である実施例[1]のシリコー
ンゲル組成物の代りとして、マイクロクリスタリンワッ
クス16部、ジメチルポリシロキサン(粘度5cs)64部に
置換した以外は同様にして製品を得た。Comparative Example [2] Foundation As an alternative to the silicone gel composition of Example [1] which is Component 4 of Example [3], except that 16 parts of microcrystalline wax and 64 parts of dimethylpolysiloxane (viscosity 5cs) were substituted. A product was obtained in the same manner.
以上の如くして得た実施例[3]と比較例[2]のフ
ァンデーションについて官能評価及び経時安定性評価を
行なった。その結果を表1に示す。The foundations of Example [3] and Comparative Example [2] obtained as described above were subjected to sensory evaluation and stability evaluation with time. The results are shown in Table 1.
なお、官能評価は女性パネル20名を用い、表1に記載
した評価項目につき非常によいを3点、良いまたはふつ
うであるを2点、悪いを1点として行ない、それぞれの
平均点が2.5点以上を◎、1.5〜2.5点未満を○、1.5点未
満を×として表わした。また経時安定性評価は室温放置
下、1週間後の外観状態を視覚観察することで行ない、
良好を○、不良を×として表わした。The sensory evaluation was carried out by using 20 female panelists, and the evaluation items listed in Table 1 were evaluated as 3 points for very good, 2 points for good or normal, and 1 point for bad, and the average score of each was 2.5 points. The above was represented by ⊚, 1.5 to less than 2.5 points by ◯, and less than 1.5 points by x. In addition, the stability with time is evaluated by visually observing the appearance state after 1 week at room temperature.
Good was represented by ○ and bad was represented by ×.
表1の結果から明らかなように本発明のファンデーシ
ョンは比較品に較べて使用感、使用性に優れたものであ
り、また比較品で経時的に油性成分の分離が認められた
のに対して安定性も良好であった。すなわち本発明によ
って構造粘性を付与するためにワックスを用いなくても
品質の高い、極めて有用な製品が得られたのであった。 As is clear from the results shown in Table 1, the foundation of the present invention is superior in feeling of use and usability as compared with the comparative product, and in the comparative product, separation of the oily component was observed with time. The stability was also good. That is, according to the present invention, a high quality and extremely useful product was obtained without using a wax for imparting structural viscosity.
実施例[4] ハンドクリーム (処方) (重量部) 1.実施例[1]のシリコーンゲル組成物 88.0 2.オクタメチルシクロテトラシロキサン 10.0 3.ワセリン 2.0 (製法) 成分1〜3を混合後、充分混練して均質にした後、容
器に充填して製品を得た。Example [4] Hand cream (prescription) (parts by weight) 1. Silicone gel composition of Example [1] 88.0 2. Octamethylcyclotetrasiloxane 10.0 3. Vaseline 2.0 (production method) After mixing components 1 to 3, After thoroughly kneading and homogenizing, the product was filled in a container.
以上の如くして得た実施例[4]のハンドクリーム
は、べたつきがなくさっぱりした感触を有するとともに
撥水効果が高く極めて有用なものであった。The hand cream of Example [4] obtained as described above was extremely useful because it had a non-sticky feel, a refreshing feel, and a high water repellency effect.
実施例[5] フェイスクリーム (処方) (重量部) 1.ステアリン酸 2.5 2.セチルアルコール 1.7 3.本発明のシリコーンゲル組成物* 20.0 4.セスキオレイン酸ソルビタン 1.0 5.モノオレイン酸ポリオキシエチレンソルビタン 2.0 6.トリエタノールアミン 0.7 7.1,3−ブチレングリコール 5.0 8.ポリメタクリル酸 0.5 9.精製水 残量 *実施例[1]に於いて低粘度シリコーン油としてオ
クタメチルシクロテトラシロキサンを用いた以外は同様
にして調製した。Example [5] Face cream (prescription) (parts by weight) 1. Stearic acid 2.5 2. Cetyl alcohol 1.7 3. Silicone gel composition of the present invention * 20.0 4. Sorbitan sesquioleate 1.0 5. Polyoxyethylene monooleate Sorbitan 2.0 6. Triethanolamine 0.7 7.1,3-butylene glycol 5.0 8. Polymethacrylic acid 0.5 9. Purified water Remaining amount * Except that octamethylcyclotetrasiloxane was used as the low viscosity silicone oil in Example [1]. Was similarly prepared.
(製法) 成分1〜5を混合し、80℃に加熱溶解し油相成分とす
る。また成分6〜9を混合し、80℃に加熱し水相成分と
する。この油相成分に水相成分を攪拌しながら添加し、
乳化を行い、冷却した後、容器に充填して製品を得た。(Manufacturing method) Components 1 to 5 are mixed and dissolved by heating at 80 ° C to obtain an oil phase component. Further, the ingredients 6 to 9 are mixed and heated to 80 ° C. to obtain an aqueous phase ingredient. Add the water phase component to this oil phase component while stirring,
After emulsification and cooling, the product was filled in a container.
以上の如くして得た実施例[5]のフェイスクリーム
は、伸びがよく、感触的にあぶらっぽさを感じず、さっ
ぱりしており、良好な使用感、使用性を有する皮膚の保
護のために有用なものであり、また経時安定性も良好で
あった。The face cream of Example [5] obtained as described above has good spreadability, feels no oily feel, is refreshing, and has a good feeling of use and usability for skin protection. Therefore, it was useful, and the stability over time was good.
[発明の効果] 以上、詳述した如く、本発明によって得られたシリコ
ーンゲル組成物は、経時安定性が良好で、しかも伸びが
よくべたつきが少なくさっぱりした感触を有し、ソフト
で軟らかな使用性に優れたものである。[Effects of the Invention] As described in detail above, the silicone gel composition obtained by the present invention has good stability over time, has good elongation, is less sticky, has a refreshing feel, and is soft and soft in use. It has excellent properties.
また、本発明のシリコーンゲル組成物は、適度な粘性
物とすることができるとともに構造粘性をもち、更には
潤滑性、撥水性に優れ、皮膚安全性が高い等、極めて有
用な性質を具備したものである。Further, the silicone gel composition of the present invention has an extremely useful property such that it can be made into a moderately viscous substance and has a structural viscosity, and further, it has excellent lubricity and water repellency and high skin safety. It is a thing.
従って、かようなシリコーンゲル組成物を化粧品用素
材として用いたならば従来シリコーン油と同様に各種の
化粧料に適用でき、その特有の性能が発揮された化粧料
が得られる。Therefore, if such a silicone gel composition is used as a cosmetic material, it can be applied to various cosmetics in the same manner as the conventional silicone oil, and a cosmetic exhibiting its unique performance can be obtained.
このことは、たとえ多量に用いてもべたつきが感じら
れず、伸びがよくてさっぱりした使用感のある、そして
また撥水性があって、皮膚や毛髪に適度な潤いと保護効
果を与えることでき、更にメーキャップ化粧料の化粧も
ちの向上をも図れることになる。This means that even if it is used in a large amount, it does not feel sticky, it has a good stretch and has a refreshing feeling of use, and it also has water repellency, and can give a proper moisturizing and protective effect to the skin and hair, Furthermore, the makeup lasting effect of makeup cosmetics can be improved.
しかも、従来ワックスを主要とする固型ないしペース
ト状油性化粧料において、あぶらっぽさを減少せしめる
ことができ、またこの種の製品系に低粘度シリコーン油
を配合した場合にあった油剤の分離が認められることも
なく、安定性を向上させうるとともに構造粘性のあるシ
リコーンをベースとした製品への応用、展開もできる。Moreover, in the solid or pasty oily cosmetics mainly composed of wax, the oiliness can be reduced, and the separation of the oil agent, which is the case when a low-viscosity silicone oil is blended in this type of product system, is also possible. It is possible to improve stability and apply and develop it to products based on silicone having structural viscosity.
このように、本発明によって、化粧品用素材として利
用度の高いシリコーンゲル組成物及び該シリコーンゲル
組成物を配合することで安定性がよく、使用感、使用性
の優れた、品質の高い化粧料の提供が可能となったので
ある。As described above, according to the present invention, a silicone gel composition having a high degree of use as a cosmetic material, and a high-quality cosmetic composition having excellent stability, excellent usability and usability by blending the silicone gel composition. Is now possible.
Claims (2)
上のベンゼンを含みうる、R2SiO単位とRSiO1.5単位の比
率が1〜30:1である三次元架橋構造を有するシリコーン
重合物と、50cs以下の低粘度シリコーン油とからなり、
かつ、シリコーン重合物と低粘度シリコーン油との重量
比率が5:95〜30:70であることを特徴とするシリコーン
ゲル組成物。1. A silicone polymer having a three-dimensional crosslinked structure, which is insoluble in benzene but may contain benzene in an amount equal to or more than its own weight and having a ratio of R 2 SiO units to RSiO 1.5 units of 1 to 30: 1. And low viscosity silicone oil of 50cs or less,
Further, the silicone gel composition is characterized in that the weight ratio of the silicone polymer to the low-viscosity silicone oil is 5:95 to 30:70.
上のベンゼンを含みうる、R2SiO単位とRSiO1.5単位の比
率が1〜30:1である三次元架橋構造を有するシリコーン
重合物と、50cs以下の低粘度シリコーン油とからなり、
かつ、シリコーン重合物と低粘度シリコーン油との重量
比率が5:95〜30:70であるシリコーンゲル組成物を含有
することを特徴とする化粧料。2. A silicone polymer having a three-dimensional crosslinked structure, which is insoluble in benzene but may contain benzene in an amount equal to or more than its own weight and having a ratio of R 2 SiO units to RSiO 1.5 units of 1 to 30: 1. And low viscosity silicone oil of 50cs or less,
Further, a cosmetic comprising a silicone gel composition in which the weight ratio of the silicone polymer to the low-viscosity silicone oil is 5:95 to 30:70.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP63015442A JPH086035B2 (en) | 1988-01-26 | 1988-01-26 | Silicone gel composition and cosmetics containing the same |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP63015442A JPH086035B2 (en) | 1988-01-26 | 1988-01-26 | Silicone gel composition and cosmetics containing the same |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH01190757A JPH01190757A (en) | 1989-07-31 |
| JPH086035B2 true JPH086035B2 (en) | 1996-01-24 |
Family
ID=11888923
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP63015442A Expired - Fee Related JPH086035B2 (en) | 1988-01-26 | 1988-01-26 | Silicone gel composition and cosmetics containing the same |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH086035B2 (en) |
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|---|---|---|---|---|
| EP2431022A2 (en) | 2010-03-05 | 2012-03-21 | Shin-Etsu Chemical Co., Ltd. | Composition based on a cross-linked fluorine-containing silicone for a cosmetic composition |
| WO2014102862A1 (en) | 2012-12-26 | 2014-07-03 | 三好化成株式会社 | Surface-treated powder and cosmetic containing same |
| US9597268B2 (en) | 2012-12-26 | 2017-03-21 | Miyoshi Kasei, Inc. | Surface-treated and plate-like powder for cosmetic compositions and solid powdery cosmetic composition blended therewith |
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|---|---|---|---|---|
| JP3480945B2 (en) * | 1991-12-27 | 2003-12-22 | 株式会社コーセー | Solid water-in-oil type emulsified cosmetic |
| US6200964B1 (en) * | 1999-05-28 | 2001-03-13 | Neutrogena Corporation | Silicone gel containing salicylic acid |
| JP4229548B2 (en) | 1999-11-16 | 2009-02-25 | 東レ・ダウコーニング株式会社 | Cosmetics and method for producing cosmetics |
| US6444745B1 (en) | 2000-06-12 | 2002-09-03 | General Electric Company | Silicone polymer network compositions |
| JP4693260B2 (en) * | 2001-03-15 | 2011-06-01 | 株式会社コーセー | Cosmetics |
| JP2003113042A (en) * | 2001-09-28 | 2003-04-18 | Kose Corp | Oil-in-water type makeup cosmetic |
| JP4616815B2 (en) * | 2006-10-16 | 2011-01-19 | ポーラ化成工業株式会社 | A topical skin preparation that gives skin smoothness |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS62134034A (en) * | 1985-12-06 | 1987-06-17 | 君塚 福松 | Fish tank cooling apparatus |
-
1988
- 1988-01-26 JP JP63015442A patent/JPH086035B2/en not_active Expired - Fee Related
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP2431022A2 (en) | 2010-03-05 | 2012-03-21 | Shin-Etsu Chemical Co., Ltd. | Composition based on a cross-linked fluorine-containing silicone for a cosmetic composition |
| WO2014102862A1 (en) | 2012-12-26 | 2014-07-03 | 三好化成株式会社 | Surface-treated powder and cosmetic containing same |
| US9597269B2 (en) | 2012-12-26 | 2017-03-21 | Miyoshi Kasei, Inc. | Surface-treated powders and cosmetic compositions in which such powders are mixed |
| US9597268B2 (en) | 2012-12-26 | 2017-03-21 | Miyoshi Kasei, Inc. | Surface-treated and plate-like powder for cosmetic compositions and solid powdery cosmetic composition blended therewith |
Also Published As
| Publication number | Publication date |
|---|---|
| JPH01190757A (en) | 1989-07-31 |
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