JPH06234918A - Oil-in-water silicone emulsion composition - Google Patents

Oil-in-water silicone emulsion composition

Info

Publication number
JPH06234918A
JPH06234918A JP5023015A JP2301593A JPH06234918A JP H06234918 A JPH06234918 A JP H06234918A JP 5023015 A JP5023015 A JP 5023015A JP 2301593 A JP2301593 A JP 2301593A JP H06234918 A JPH06234918 A JP H06234918A
Authority
JP
Japan
Prior art keywords
component
organopolysiloxane
group
water
components
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
Application number
JP5023015A
Other languages
Japanese (ja)
Other versions
JP3020373B2 (en
Inventor
Shiyuuichi Azechi
秀一 畔地
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Shin Etsu Chemical Co Ltd
Original Assignee
Shin Etsu Chemical Co Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Shin Etsu Chemical Co Ltd filed Critical Shin Etsu Chemical Co Ltd
Priority to JP5023015A priority Critical patent/JP3020373B2/en
Priority to TW082108283A priority patent/TW289040B/zh
Priority to KR1019940002414A priority patent/KR100275645B1/en
Publication of JPH06234918A publication Critical patent/JPH06234918A/en
Application granted granted Critical
Publication of JP3020373B2 publication Critical patent/JP3020373B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L59/00Compositions of polyacetals; Compositions of derivatives of polyacetals
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L33/00Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
    • C08L33/04Homopolymers or copolymers of esters

Abstract

PURPOSE:To obtain an emulsion compsn. excellent in the feeling of use and in emulsion stability and suitable for cosmetics, a base material of a medicine, etc., by emulsifying organopolysiloxanes, polyoxyalkylene-modified organopolysiloxane, and an ionic surfactant in water. CONSTITUTION:The compsn. is prepd. by emulsifying, in water, an organopolysiloxane of the formula (wherein R is a 1-6C monovalent hydrocarbon group; and n is, on an average, 500-10,000) (A), an organopolysiloxane having a viscosity index at 25 deg.C of 1-500cSt (B1), a polyoxyalkylene-modified organopolysiloxane having an HLB value of 5-12 (C), and an ionic surfactant (D) in a wt. ratio of the sum of components A and B to the sum of components C and D of (95:5)-(50:50) and in a wt. ratio of component D to the sum of components C and D of 0.5-20wt.%.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明は、使用感が良好で、かつ
乳化安定性に優れ、シャンプー、リンス等の毛髪化粧料
やクリーム、乳液等の皮膚化粧料、更に軟膏等の医薬品
用基剤として好適に使用できる水中油型シリコーン乳化
組成物に関する。
FIELD OF THE INVENTION The present invention relates to a cosmetic for hair cosmetics such as shampoos and rinses, skin cosmetics such as creams and emulsions, and a base for pharmaceuticals such as ointments, etc. The present invention relates to an oil-in-water type silicone emulsion composition that can be preferably used as.

【0002】[0002]

【従来の技術】従来、皮膚あるいは毛髪用化粧料には、
滑らかさや毛髪に光沢を与えるなどの目的でシリコーン
油、シリコーン樹脂が使用されている(特開昭61−1
61209号、同61−161211号、同61−16
1214号、同63−246309号、同63−246
310号、同63−183515号、同63−1835
16号、同63−183517号、同63−24301
8号、同63−243019号、同63−246309
号、同63−246310号、同63−313712
号、同63−316713号、同63−316718
号、同64−75416号、特開平1−203314
号、同1−211515号、同1−211517号、同
1−211518号公報参照)。
2. Description of the Related Art Conventionally, cosmetics for skin or hair are
Silicone oil and silicone resin are used for the purpose of imparting smoothness and luster to hair (JP-A-61-1).
61209, 61-161211 and 61-16.
1214, 63-246309, 63-246.
No. 310, No. 63-183515, No. 63-1835
No. 16, No. 63-183517, No. 63-24301
No. 8, 63-243019, 63-246309.
No. 63, No. 63-246310, No. 63-313712
No. 63-316713 and No. 63-316718.
No. 64-75416, JP-A-1-203314.
Nos. 1-211515, 1-211517, and 1-211518).

【0003】[0003]

【発明が解決しようとする課題】しかしながら、シリコ
ーン油、シリコーン樹脂を配合した皮膚あるいは毛髪用
化粧料は、皮膚あるいは毛髪への密着性が不十分であっ
たり、べたつきが残るという欠点を有しており、使用性
に劣るものであった。また、これらの化粧料用シリコー
ン油、シリコーン樹脂は、通常炭化水素系界面活性剤を
使用して水に乳化分散されるが、高剪断力の乳化分散装
置を使用しないと安定したエマルジョン粒子を得ること
ができないという不利があった。従って、使用性及び保
存安定性に優れたシリコーンエマルジョン粒子を与える
乳化用組成物及びこれを用いた水中油型シリコーン乳化
組成物の開発が望まれていた。本発明は上記要望に応え
るためになされたもので、使用性に優れ、かつ粒径が小
さく長期保存後においても安定なエマルジョン粒子から
なる水中油型シリコーン乳化組成物を提供することを目
的とする。
However, the cosmetics for skin or hair containing silicone oil or silicone resin have drawbacks such as insufficient adhesion to the skin or hair and stickiness remaining. And was inferior in usability. Moreover, these silicone oils for cosmetics and silicone resins are usually emulsified and dispersed in water using a hydrocarbon-based surfactant, but stable emulsion particles are obtained unless an emulsifying and dispersing device with high shearing force is used. There was a disadvantage that you couldn't. Therefore, it has been desired to develop an emulsifying composition which gives silicone emulsion particles excellent in usability and storage stability, and an oil-in-water type silicone emulsion composition using the same. The present invention has been made in order to meet the above-mentioned demands, and an object thereof is to provide an oil-in-water type silicone emulsion composition which is excellent in usability and has a small particle size and is stable even after long-term storage. .

【0004】[0004]

【課題を解決するための手段及び作用】本発明者らは上
記課題を解決するため鋭意検討を重ねた結果、(1)下
記一般式(I)で示される高重合度のオルガノポリシロ
キサン
Means and Actions for Solving the Problems As a result of intensive studies to solve the above problems, the present inventors have found that (1) an organopolysiloxane having a high degree of polymerization represented by the following general formula (I).

【化2】 (但し、式中のRは炭素数1〜6の1価炭化水素基であ
り、nは平均値で500〜10000の数である。)
と、(2)25℃における粘度が1〜500cs(セン
チストークス)の中〜低分子オルガノポリシロキサン
と、(3)シリコーン系界面活性剤としてHLB値が5
〜12のポリオキシアルキレン変性オルガノポリシロキ
サンと、(4)イオン性界面活性剤とから基本的にな
り、重量比で[(1)成分+(2)成分]/[(3)成
分+(4)成分]=95/5〜50/50の範囲にあ
り、かつ(4)成分が[(3)成分+(4)成分]中
0.5〜20重量%含有されるようにして、水中に乳化
することにより、皮膚及び毛髪への密着性に優れかつ皮
膚等へ伸展後の皮膜がべたつくこともなく使用性に優
れ、しかも刺激性が少なく安全性が高い上、炭化水素系
界面活性剤を配合した場合のように高剪断力の乳化分散
装置を用いなくても小さい粒径のエマルジョン粒子が均
一に分散して保存安定性に優れた水中油型シリコーン乳
化組成物が得られることを知見し、本発明をなすに至っ
た。
[Chemical 2] (However, R in the formula is a monovalent hydrocarbon group having 1 to 6 carbon atoms, and n is an average value of 500 to 10,000.)
And (2) a medium to low molecular weight organopolysiloxane having a viscosity at 25 ° C. of 1 to 500 cs (centistokes), and (3) an HLB value of 5 as a silicone-based surfactant.
To 12 of polyoxyalkylene-modified organopolysiloxane and (4) ionic surfactant, and the weight ratio of [(1) component + (2) component] / [(3) component + (4 Component) = 95/5 to 50/50, and the component (4) is contained in water in an amount of 0.5 to 20% by weight in the component (3) + (4). By emulsifying, it has excellent adhesion to the skin and hair, and it has excellent usability without sticking of the film after spreading on the skin, etc., and it has low irritation and high safety. It was found that an oil-in-water type silicone emulsion composition having excellent storage stability can be obtained by uniformly dispersing emulsion particles having a small particle size without using an emulsifying and dispersing device having a high shearing force as in the case of blending. The present invention has been completed.

【0005】以下、本発明につき更に詳細に説明する。
本発明の水中油型シリコーン乳化組成物の第1必須成分
は、下記一般式(I)で示される高重合度のオルガノポ
リシロキサンである。
The present invention will be described in more detail below.
The first essential component of the oil-in-water silicone emulsion composition of the present invention is a high degree of polymerization organopolysiloxane represented by the following general formula (I).

【化3】 (但し、式中のRは炭素数1〜6の1価炭化水素基であ
り、nは平均値で500〜10000の数である。)
[Chemical 3] (However, R in the formula is a monovalent hydrocarbon group having 1 to 6 carbon atoms, and n is an average value of 500 to 10,000.)

【0006】ここで、式中のRは炭素数1〜6の1価炭
化水素基であり、例えばメチル基、エチル基、プロピル
基、ブチル基、ペンチル基、ヘキシル基、シクロヘキシ
ル基、フェニル基などが挙げられるが、特にメチル基が
R中の90モル%以上であることが望ましい。また、n
は平均重合度で500〜10000、好ましくは100
0〜7000の数であり、500より小さいと得られる
皮膜の密着性が劣る場合があり、10000より大きい
ものは工業的に得ることが難しい場合がある。
Here, R in the formula is a monovalent hydrocarbon group having 1 to 6 carbon atoms, such as methyl group, ethyl group, propyl group, butyl group, pentyl group, hexyl group, cyclohexyl group and phenyl group. However, it is particularly desirable that the methyl group is 90 mol% or more of R. Also, n
Is an average degree of polymerization of 500 to 10,000, preferably 100.
It is a number from 0 to 7,000, and if it is less than 500, the adhesion of the obtained film may be poor, and if it is more than 10,000, it may be difficult to obtain industrially.

【0007】上記オルガノポリシロキサンの配合量は、
組成物全体の0.1〜20%(重量%、以下同様)とす
ることが好ましく、5〜15%とすることが特に好まし
い。配合量が0.1%に満たないと得られる皮膜の密着
性が低く、かつ耐擦傷性が不十分なものとなる場合があ
り、20%を超えると皮膚への伸展性が低く、乾燥した
皮膜はべたつきの多い場合がある。
The amount of the above organopolysiloxane compounded is
It is preferably 0.1 to 20% (% by weight, the same applies hereinafter) of the entire composition, and particularly preferably 5 to 15%. If the blending amount is less than 0.1%, the adhesion of the obtained film may be low and the scratch resistance may be insufficient, and if it exceeds 20%, the extensibility to the skin is low and the film is dried. The coating may be sticky in many cases.

【0008】次に、第2必須成分は、25℃における粘
度が1〜500csの中〜低分子オルガノポリシロキサ
ンである。この中〜低分子オルガノポリシロキサンは環
状でも線状でも分岐状でもよく、環状のオルガノポリシ
ロキサンとしては、下記一般式(II)で示されるものが
好適に使用される。
The second essential component is a medium to low molecular weight organopolysiloxane having a viscosity at 25 ° C. of 1 to 500 cs. The medium to low molecular weight organopolysiloxane may be cyclic, linear or branched, and as the cyclic organopolysiloxane, those represented by the following general formula (II) are preferably used.

【化4】 (但し、式中のRは前記と同様炭素数1〜6の1価炭化
水素基であり、pは3〜6の数である。)
[Chemical 4] (However, R in the formula is a monovalent hydrocarbon group having 1 to 6 carbon atoms as described above, and p is a number of 3 to 6.)

【0009】また、線状のオルガノポリシロキサンとし
ては、下記一般式(III) で示されるものが好適に使用さ
れる。
As the linear organopolysiloxane, those represented by the following general formula (III) are preferably used.

【化5】 (但し、式中のRは前記と同様炭素数1〜6の1価炭化
水素基であり、qは1〜250の数である。)
[Chemical 5] (However, R in the formula is a monovalent hydrocarbon group having 1 to 6 carbon atoms as described above, and q is a number of 1 to 250.)

【0010】更に、分岐状のオルガノポリシロキサンと
しては、本質的にR3 SiO1/2 単位とRSiO3/2
位及びR2 SiO単位とからなるものが好適に使用され
る。(但し、式中のRは前記と同様炭素数1〜6の1価
炭化水素基である。)
Furthermore, as the branched organopolysiloxane, those essentially consisting of R 3 SiO 1/2 units, RSiO 3/2 units and R 2 SiO units are preferably used. (However, R in the formula is a monovalent hydrocarbon group having 1 to 6 carbon atoms as described above.)

【0011】上記オルガノポリシロキサンは25℃にお
ける粘度が1〜500csのものとするが、好ましくは
2〜400csのものである。1csに満たないと第1
成分の溶解性が悪くなり、500csを超えると皮膜形
成能が低下する。第2成分としての上記オルガノポリシ
ロキサンは1種類を単独で用いてもよいし、2種類以上
を併用することもできる。また、この第2成分の配合量
は、組成物全体の5〜70%、特に20〜50%である
ことが好ましく、配合量が5%に満たないと第1成分の
溶解性、乳化性が悪化する場合があり、70%を超える
と組成物の皮膜形成能が低下する場合がある。
The organopolysiloxane has a viscosity at 25 ° C. of 1 to 500 cs, preferably 2 to 400 cs. First less than 1cs
The solubility of the components deteriorates, and if it exceeds 500 cs, the film forming ability decreases. The organopolysiloxane as the second component may be used alone or in combination of two or more. Further, the content of the second component is preferably 5 to 70%, particularly preferably 20 to 50% of the entire composition, and if the content is less than 5%, the solubility and emulsification of the first component will be poor. It may deteriorate, and if it exceeds 70%, the film-forming ability of the composition may decrease.

【0012】本発明においては、第3必須成分としてポ
リオキシアルキレン変性オルガノポリシロキサンを配合
するが、そのHLB値は5〜12、好ましくは6〜9で
ある。HLB値が5より小さくても12より大きくても
得られる乳化組成物が安定性に乏しくなる。なお、ここ
でHLB値は下記計算式から算出される値である。 (分子中に占める CH2CH2O基の重量%)/5=HLB値
In the present invention, a polyoxyalkylene-modified organopolysiloxane is blended as the third essential component, and its HLB value is 5-12, preferably 6-9. When the HLB value is smaller than 5 or larger than 12, the emulsion composition obtained has poor stability. The HLB value here is a value calculated from the following calculation formula. (% By weight of CH 2 CH 2 O groups in the molecule) / 5 = HLB value

【0013】このようなポリオキシアルキレン変性オル
ガノポリシロキサンとしては下記一般式(IV)で示され
るものが好適に使用される。
As such a polyoxyalkylene-modified organopolysiloxane, those represented by the following general formula (IV) are preferably used.

【化6】 [但し、式中のGは下記式 -(CH2)t-O-(R1O)u-Q (式中、R1はエチレン基又はプロピレン基から少なくと
も一つは選ばれる基であり、Qは水素原子又は炭素数1
〜8のアルキル基、アセチル基、イソシアン基から選択
される1価の有機基、tは2〜6、uは3〜50であ
る。)で示される分子量が200〜3000の基であ
り、aは0又は1、rは10〜150、sは1〜50で
ある。]その具体例としては後記実施例で示した化合物
が挙げられる。
[Chemical 6] [Wherein G is the following formula:-(CH 2 ) t -O- (R 1 O) u -Q (In the formula, R 1 is a group selected from at least one of an ethylene group and a propylene group, Q is a hydrogen atom or 1 carbon atom
~ 8 is a monovalent organic group selected from an alkyl group, an acetyl group, and an isocyanate group, t is 2 to 6, and u is 3 to 50. ) Is a group having a molecular weight of 200 to 3000, a is 0 or 1, r is 10 to 150, and s is 1 to 50. Specific examples thereof include the compounds shown in Examples below.

【0014】また、本発明で使用するポリオキシアルキ
レン変性オルガノポリシロキサンは粘度が100〜30
00csであることが好ましい。
The polyoxyalkylene-modified organopolysiloxane used in the present invention has a viscosity of 100 to 30.
It is preferably 00 cs.

【0015】第3成分のポリオキシアルキレン変性オル
ガノポリシロキサンの配合量は、組成物全体の1〜50
%、特に5〜30%とすることが好ましく、1%より少
ないと安定な乳化組成物が得られない場合があり、50
%より多いと得られる皮膜がべたつきの多いものとなる
場合がある。
The blending amount of the third component, the polyoxyalkylene-modified organopolysiloxane, is 1 to 50 of the total composition.
%, Particularly 5 to 30% is preferable, and if it is less than 1%, a stable emulsion composition may not be obtained.
If it is more than%, the resulting film may become sticky.

【0016】本発明の組成物の第4必須成分であるイオ
ン性界面活性剤としては、イオン性基を含有し、化粧料
原料、医薬品原料等に使用できるものであれば、アニオ
ン性、カチオン性、両性いずれのタイプの界面活性剤で
も使用できる。
As the ionic surfactant which is the fourth essential component of the composition of the present invention, any ionic surfactant may be used as long as it contains an ionic group and can be used as a raw material for cosmetics, a raw material for pharmaceuticals and the like. Any type of amphoteric surfactant can be used.

【0017】このようなイオン性界面活性剤としては、
アニオン性界面活性剤の例えば直鎖アルコール硫酸エス
テル塩、側鎖アルコール硫酸エステル塩、アルキルエー
テル硫酸エステル塩、グリセリン脂肪酸エステルの硫酸
エステル塩、高級脂肪酸アルキロールアミドの硫酸エス
テル塩等の硫酸エステル塩、アルカンスルホン酸塩、オ
レフィンスルホン酸塩、高級脂肪酸エステルのスルホン
酸塩、ジアルキルスルホコハク酸塩、高級脂肪酸アミド
のスルホン酸塩、アルキルアリールスルホン酸塩等のス
ルホン酸塩、脂肪酸石けん、エーテルカルボン酸塩等の
カルボン酸塩、りん酸エステル塩、高級脂肪酸とアミノ
酸の縮合物、コラーゲン加水分解物誘導体などが挙げら
れる。
As such an ionic surfactant,
Anionic surfactants, for example, straight-chain alcohol sulfuric acid ester salts, side-chain alcohol sulfuric acid ester salts, alkyl ether sulfuric acid ester salts, sulfuric acid ester salts of glycerin fatty acid ester, sulfuric acid ester salts of higher fatty acid alkylolamide, etc., Alkane sulfonates, olefin sulfonates, sulfonates of higher fatty acid esters, dialkyl sulfosuccinates, sulfonates of higher fatty acid amides, sulfonates such as alkylaryl sulfonates, fatty acid soaps, ether carboxylates, etc. Carboxylic acid salts, phosphoric acid ester salts, condensates of higher fatty acids and amino acids, collagen hydrolyzate derivatives, and the like.

【0018】また、カチオン性界面活性剤の例えばアル
キルアミン塩、ポリアミン及びアルカノールアミン脂肪
酸誘導体等のアミン塩、アルキルトリメチルアンモニウ
ム塩、ジアルキルジメチルアンモニウム塩、アルキルジ
メチルベンジルアンモニウム塩等のアルキル四級アンモ
ニウム塩、アルキルピリジニウム塩、アルキルイソキノ
リニウム塩、ジアルキルモルホリニウム塩等の環式四級
アンモニウム塩、塩化ベンゼトニウムなどが挙げられ
る。
In addition, cationic surfactants such as alkylamine salts, amine salts such as polyamine and alkanolamine fatty acid derivatives, alkyl quaternary ammonium salts such as alkyl trimethyl ammonium salts, dialkyl dimethyl ammonium salts, and alkyl dimethyl benzyl ammonium salts, Examples thereof include cyclic quaternary ammonium salts such as alkylpyridinium salts, alkylisoquinolinium salts and dialkylmorpholinium salts, and benzethonium chloride.

【0019】また、両性界面活性剤の例えばカルボン酸
型(アミノ酸型、ベタイン型)、硫酸エステル型、スル
ホン酸型、レシチン等のりん酸エステル型などが挙げら
れる。
Examples of the amphoteric surfactant include carboxylic acid type (amino acid type, betaine type), sulfuric acid ester type, sulfonic acid type, and phosphoric acid ester type such as lecithin.

【0020】上記第4成分のイオン性界面活性剤を用い
ることにより、安定性に優れた乳化組成物が得られる
が、この第4成分の配合量は[第3成分+第4成分]中
0.5〜20重量%含有されるようにする。0.5重量
%未満では得られる乳化組成物の安定性が乏しいものと
なるし、20重量%より多いと得られる皮膜がべたつき
の多いものとなる。好ましくは1〜10重量%の範囲で
ある。
By using the ionic surfactant as the fourth component, an emulsion composition having excellent stability can be obtained. The content of the fourth component is 0 in [third component + fourth component]. 0.5 to 20% by weight. If it is less than 0.5% by weight, the stability of the obtained emulsion composition will be poor, and if it is more than 20% by weight, the film obtained will be sticky. It is preferably in the range of 1 to 10% by weight.

【0021】また、同時に第1〜4成分は重量比で[第
1成分+第2成分]/[第3成分+第4成分]=95/
5〜50/50、好ましくは92/8〜60/40とな
るように配合する。この配合比が95/5より大きいと
得られる乳化組成物が安定性の乏しいものとなり、50
/50よりも小さいと得られる皮膜がべたつきの多いも
のとなる。
At the same time, the weight ratio of the first to fourth components is [first component + second component] / [third component + fourth component] = 95 /
It is blended so as to be 5 to 50/50, preferably 92/8 to 60/40. If this blending ratio exceeds 95/5, the resulting emulsion composition will have poor stability, and
When it is less than / 50, the obtained film becomes sticky.

【0022】本発明の水中油型シリコーン乳化組成物
は、上記第1〜4成分と水とを所定量混合することによ
り得ることができる。この場合、各成分の混合順序に特
に制限はないが、まず第1、2成分を混合した後、攪拌
又はホモミキサー等の機械を用いて第3、4成分を添加
・混合し、更に水を添加・混合することが好適である。
なお、各成分の混合時の温度は70℃以下に調整するこ
とが望ましい。
The oil-in-water silicone emulsion composition of the present invention can be obtained by mixing the above-mentioned first to fourth components with water in a predetermined amount. In this case, the mixing order of each component is not particularly limited, but first, the first and second components are mixed, then the third and fourth components are added and mixed using a machine such as stirring or a homomixer, and water is further added. It is preferable to add and mix.
The temperature at the time of mixing the components is preferably adjusted to 70 ° C or lower.

【0023】[0023]

【実施例】以下、実施例及び比較例を示して本発明を具
体的に説明するが、本発明は下記実施例に制限されるも
のではない。なお、各例中の%はいずれも重量%であ
る。 [実施例1〜17、比較例1〜9]表1に示す水以外の
各成分を攪拌混合した後、水を徐々に添加してホモミキ
サー攪拌を行い水中油型シリコーン乳化組成物を得た。
これら組成物の40℃における保存安定性及び粒径と使
用感を下記方法で測定した。結果を表2に示す。
EXAMPLES The present invention will be specifically described below with reference to Examples and Comparative Examples, but the present invention is not limited to the following Examples. In addition,% in each example is% by weight. [Examples 1 to 17 and Comparative Examples 1 to 9] After stirring and mixing each component other than water shown in Table 1, water was gradually added and the mixture was stirred with a homomixer to obtain an oil-in-water silicone emulsion composition. .
The storage stability at 40 ° C., the particle size and the feeling of use of these compositions were measured by the following methods. The results are shown in Table 2.

【0024】保存安定性試験方法:40℃で保存し、経
時での分離性を目視観察した。 粒径測定方法:Submicron Particle Analyzer Coulter
Model N4を用いて測定した。 使用感評価方法:皮膚に伸展した後、乾燥した皮膜の使
用感を官能評価した。 ○:べたつきがなくさっぱりしている。 ×:べたつきが大きい。
Storage stability test method: Stored at 40 ° C., and visually observed for separability over time. Particle size measurement method: Submicron Particle Analyzer Coulter
It measured using Model N4. Evaluation method of feeling of use: After being spread on the skin, the feeling of use of the dried film was sensory evaluated. ○: There is no stickiness and it is refreshing. X: Sticky is large.

【0025】なお、実施例及び比較例で用いた成分は下
記のとおりである。 [第1成分]
The components used in the examples and comparative examples are as follows. [First component]

【化7】 (a)上記一般式(I)においてRがCH3 基でn=3
500のジメチルポリシロキサン。 (b)上記一般式(I)においてRがCH3 基でn=4
200のジメチルポリシロキサン。
[Chemical 7] (A) In the above general formula (I), R is a CH 3 group and n = 3.
500 dimethyl polysiloxane. (B) In the general formula (I), R is a CH 3 group and n = 4.
200 dimethyl polysiloxane.

【0026】[第2成分][Second component]

【化8】 (a)上記一般式(III) においてRがCH3 基、q=2
7であり、25℃での粘度が20csであるジメチルポ
リシロキサン。 (b)上記一般式(III) においてRがCH3 基、q=1
50であり、25℃での粘度が200csであるジメチ
ルポリシロキサン。 (c)上記一般式(II)においてRがCH3 基、p=5で
あり、25℃での粘度が4csである環状シロキサン1
2%と25℃での粘度が15csでフェニル基含有量が
30モル%である直鎖及び分岐状のメチルフェニルシロ
キサン88%の混合物。
[Chemical 8] (A) In the general formula (III), R is a CH 3 group, q = 2
Dimethylpolysiloxane having a viscosity of 7 and a viscosity at 25 ° C. of 20 cs. (B) In the general formula (III), R is a CH 3 group, q = 1
Dimethyl polysiloxane having a viscosity of 50 and a viscosity of 200 cs at 25 ° C. (C) Cyclic siloxane 1 in which R is CH 3 group, p = 5, and viscosity at 25 ° C. is 4 cs in the general formula (II).
A mixture of 2% and 88% linear and branched methylphenylsiloxanes having a viscosity of 15 cs at 25 ° C. and a phenyl group content of 30 mol%.

【0027】[第3成分] (a)下記式で示され、25℃での粘度が1600cs
であり、HLB値が6.3であるポリオキシアルキレン
変性ジメチルポリシロキサン。
[Third component] (a) It is represented by the following formula and has a viscosity at 25 ° C. of 1600 cs.
And a polyoxyalkylene-modified dimethylpolysiloxane having an HLB value of 6.3.

【化9】 [Chemical 9]

【0028】(b)下記式で示され、25℃での粘度が
400csであり、HLB値が8.5であるポリオキシ
アルキレン変性ジメチルポリシロキサン。
(B) A polyoxyalkylene-modified dimethylpolysiloxane represented by the following formula, having a viscosity at 25 ° C. of 400 cs and an HLB value of 8.5.

【化10】 [Chemical 10]

【0029】(c)下記式で示され、25℃での粘度が
220csであり、HLB値が3.5であるポリオキシ
アルキレン変性ジメチルポリシロキサン(比較品)。
(C) A polyoxyalkylene-modified dimethylpolysiloxane (comparative product) represented by the following formula, having a viscosity at 25 ° C. of 220 cs and an HLB value of 3.5.

【化11】 [Chemical 11]

【0030】(d)下記式で示され、25℃での粘度が
100csであり、HLB値が12.5であるポリオキ
シアルキレン変性ジメチルポリシロキサン(比較品)。
(D) A polyoxyalkylene-modified dimethylpolysiloxane represented by the following formula, having a viscosity at 25 ° C. of 100 cs and an HLB value of 12.5 (comparative product).

【化12】 [Chemical 12]

【0031】(e)下記式で示され、25℃での粘度が
130csであり、HLB値が16.1であるポリオキ
シアルキレン変性ジメチルポリシロキサン(比較品)。
(E) A polyoxyalkylene-modified dimethylpolysiloxane (comparative product) represented by the following formula, having a viscosity at 25 ° C. of 130 cs and an HLB value of 16.1.

【化13】 [Chemical 13]

【0032】[第4成分] (a)ポリオキシエチレン(EO3)ドデシルエーテル
硫酸ナトリウム (b)ドデシル硫酸ナトリウム (c)セチル硫酸ナトリウム (d)ポリオキシエチレン(EO3)トリデシルエーテ
ル酢酸ナトリウム (e)ポリオキシエチレン(EO5)セチルエーテルり
ん酸ナトリウム (f)塩化セチルトリメチルアンモニウム (g)塩化ステアリルトリメチルアンモニウム (h)ラウリル酢酸ベタイン
[Fourth Component] (a) Polyoxyethylene (EO3) sodium dodecyl ether sulfate (b) Sodium dodecyl sulfate (c) Sodium cetyl sulfate (d) Polyoxyethylene (EO3) sodium tridecyl ether acetate (e) Sodium polyoxyethylene (EO5) cetyl ether phosphate (f) Cetyltrimethylammonium chloride (g) Stearyltrimethylammonium chloride (h) Betaine lauryl acetate

【0033】[0033]

【表1】 [Table 1]

【0034】[0034]

【表2】 [Table 2]

【0035】本発明のシリコーン乳化組成物は実施例か
らも明らかなとおり、エマルジョン粒子の粒径が小さく
保存安定性に優れたものであり、しかも皮膚に伸展後、
乾燥した皮膜は密着性に優れ、べたつきのないさっぱり
としたものであることが確認された。これに対し、比較
例1〜6及び成分の配合比が本発明の範囲外である比較
例7の組成物は、粒径が大きく保存安定性に乏しいもの
であり、また、成分の配合比が本発明の範囲外である比
較例8の組成物は保存安定性が良好であるものの、皮膚
に伸展後、乾燥した皮膜はべたつきの大きいものであっ
た。さらに、第4成分の少ない比較例9の組成物も安定
性の乏しいものであった。
As is clear from the examples, the silicone emulsion composition of the present invention has a small emulsion particle size and is excellent in storage stability, and after spreading on the skin,
It was confirmed that the dried film had excellent adhesion and was a non-sticky, refreshing film. On the other hand, the compositions of Comparative Examples 1 to 6 and the composition of Comparative Example 7 in which the compounding ratio of the components is out of the range of the present invention have large particle size and poor storage stability, and the compounding ratio of the components is The composition of Comparative Example 8, which was outside the scope of the present invention, had good storage stability, but the dried film after spreading on the skin had a large stickiness. Furthermore, the composition of Comparative Example 9 containing a small amount of the fourth component also had poor stability.

【0036】[0036]

【発明の効果】本発明の水中油型シリコーン乳化組成物
は、皮膚及び毛髪への密着性に優れかつ皮膚等へ伸展後
の皮膜がべたつくこともなく使用性に優れ、しかも低刺
激性で安全である上、小さい粒径のエマルジョン粒子が
均一に分散して優れた保存安定性を有する。従って、本
発明の組成物は、皮膚、毛髪等に対して低刺激で光沢や
伸展性に優れた化粧基材としてシャンプー、リンス等の
毛髪化粧料、クリーム、乳液等の皮膚化粧料などに使用
し得、また医薬用途などの配合基材として軟膏等にも有
効に使用することができる。
EFFECT OF THE INVENTION The oil-in-water silicone emulsion composition of the present invention is excellent in adhesion to the skin and hair, and has excellent usability without stickiness of the film after spreading on the skin, and is safe with low irritation. In addition, the emulsion particles having a small particle size are uniformly dispersed to have excellent storage stability. Therefore, the composition of the present invention is used as a cosmetic base material having low irritation to the skin, hair and the like and excellent in gloss and spreadability, for hair cosmetics such as shampoo and conditioner, skin cosmetics such as cream and emulsion. In addition, it can be effectively used in ointments and the like as a compounding base material for pharmaceutical use.

───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.5 識別記号 庁内整理番号 FI 技術表示箇所 A61K 47/24 H 7433−4C C08L 83/12 ─────────────────────────────────────────────────── ─── Continuation of the front page (51) Int.Cl. 5 Identification code Office reference number FI Technical display area A61K 47/24 H 7433-4C C08L 83/12

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】(1)下記一般式(I)で示されるオルガ
ノポリシロキサン 【化1】 (但し、式中のRは炭素数1〜6の1価炭化水素基であ
り、nは平均値で500〜10000の数である。)、 (2)25℃における粘度が1〜500センチストーク
スのオルガノポリシロキサン、 (3)HLB値が5〜12のポリオキシアルキレン変性
オルガノポリシロキサン及び (4)イオン性界面活性剤の(1)〜(4)成分から基
本的になるものを、この(1)〜(4)成分が重量比で
[(1)成分+(2)成分]/[(3)成分+(4)成
分]=95/5〜50/50の範囲にあり、かつ(4)
成分が[(3)成分+(4)成分]中0.5〜20重量
%含有されるようにして、水に乳化してなることを特徴
とする水中油型シリコーン乳化組成物。
1. An organopolysiloxane represented by the following general formula (I): (However, R in the formula is a monovalent hydrocarbon group having 1 to 6 carbon atoms, and n is an average value of 500 to 10,000.), (2) Viscosity at 25 ° C. is 1 to 500 centistokes. (3) a polyoxyalkylene-modified organopolysiloxane having an HLB value of 5 to 12 and (4) an ionic surfactant (1) to (4), which basically comprises The weight ratio of the components 1) to 4 is [(1) component + (2) component] / [(3) component + (4) component] = 95/5 to 50/50, and (4) )
An oil-in-water type silicone emulsified composition, characterized in that it is emulsified in water such that the components are contained in an amount of 0.5 to 20% by weight in [(3) component + (4) component].
JP5023015A 1993-02-10 1993-02-10 Oil-in-water silicone emulsion composition Expired - Fee Related JP3020373B2 (en)

Priority Applications (3)

Application Number Priority Date Filing Date Title
JP5023015A JP3020373B2 (en) 1993-02-10 1993-02-10 Oil-in-water silicone emulsion composition
TW082108283A TW289040B (en) 1993-02-10 1993-10-06
KR1019940002414A KR100275645B1 (en) 1993-02-10 1994-02-08 Oil-in-water silicone emulsion composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP5023015A JP3020373B2 (en) 1993-02-10 1993-02-10 Oil-in-water silicone emulsion composition

Publications (2)

Publication Number Publication Date
JPH06234918A true JPH06234918A (en) 1994-08-23
JP3020373B2 JP3020373B2 (en) 2000-03-15

Family

ID=12098672

Family Applications (1)

Application Number Title Priority Date Filing Date
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Country Status (3)

Country Link
JP (1) JP3020373B2 (en)
KR (1) KR100275645B1 (en)
TW (1) TW289040B (en)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2002348475A (en) * 2001-05-24 2002-12-04 Ge Toshiba Silicones Co Ltd Silicone emulsion composition and cosmetic
KR100719781B1 (en) * 1999-06-21 2007-05-21 가부시키가이샤 시세이도 High internal aqueous phase water-in-oil type emulsion cosmetic composition
JP2007532644A (en) * 2004-04-15 2007-11-15 ダウ・コーニング・コーポレイション Low molecular weight silicone oil emulsion in water
WO2010074297A1 (en) 2008-12-22 2010-07-01 Dow Corning Toray Co., Ltd. Emulsion, method for producing the same, and cosmetic raw material formed from the same
WO2010074295A1 (en) 2008-12-22 2010-07-01 Dow Corning Toray Co., Ltd. Method for producing emulsion
US8686174B2 (en) 2008-12-22 2014-04-01 Dow Corning Toray Co. Ltd. Partially hydrocarbon group-blocked (poly)glycerol-modified polysiloxane, method for producing the same, and cosmetic composition containing the same

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100719781B1 (en) * 1999-06-21 2007-05-21 가부시키가이샤 시세이도 High internal aqueous phase water-in-oil type emulsion cosmetic composition
JP2002348475A (en) * 2001-05-24 2002-12-04 Ge Toshiba Silicones Co Ltd Silicone emulsion composition and cosmetic
JP2007532644A (en) * 2004-04-15 2007-11-15 ダウ・コーニング・コーポレイション Low molecular weight silicone oil emulsion in water
WO2010074297A1 (en) 2008-12-22 2010-07-01 Dow Corning Toray Co., Ltd. Emulsion, method for producing the same, and cosmetic raw material formed from the same
WO2010074295A1 (en) 2008-12-22 2010-07-01 Dow Corning Toray Co., Ltd. Method for producing emulsion
US8686174B2 (en) 2008-12-22 2014-04-01 Dow Corning Toray Co. Ltd. Partially hydrocarbon group-blocked (poly)glycerol-modified polysiloxane, method for producing the same, and cosmetic composition containing the same
US8835555B2 (en) 2008-12-22 2014-09-16 Dow Corning Toray Co. Ltd. Method for producing emulsion

Also Published As

Publication number Publication date
TW289040B (en) 1996-10-21
KR940019808A (en) 1994-09-15
JP3020373B2 (en) 2000-03-15
KR100275645B1 (en) 2000-12-15

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