JPS62234012A - Anti-suntan cosmetic - Google Patents

Anti-suntan cosmetic

Info

Publication number
JPS62234012A
JPS62234012A JP7577486A JP7577486A JPS62234012A JP S62234012 A JPS62234012 A JP S62234012A JP 7577486 A JP7577486 A JP 7577486A JP 7577486 A JP7577486 A JP 7577486A JP S62234012 A JPS62234012 A JP S62234012A
Authority
JP
Japan
Prior art keywords
volatile
oil
organic silicone
silicone polymer
absorber
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
JP7577486A
Other languages
Japanese (ja)
Other versions
JPH0811723B2 (en
Inventor
Masako Naganuma
長沼 雅子
Minoru Fukuda
実 福田
Yoshio Hachiman
八幡 佳夫
Shigenori Kumagai
重則 熊谷
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.)
Shiseido Co Ltd
Original Assignee
Shiseido 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 Shiseido Co Ltd filed Critical Shiseido Co Ltd
Priority to JP61075774A priority Critical patent/JPH0811723B2/en
Publication of JPS62234012A publication Critical patent/JPS62234012A/en
Publication of JPH0811723B2 publication Critical patent/JPH0811723B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q17/00Barrier preparations; Preparations brought into direct contact with the skin for affording protection against external influences, e.g. sunlight, X-rays or other harmful rays, corrosive materials, bacteria or insect stings
    • A61Q17/04Topical preparations for affording protection against sunlight or other radiation; Topical sun tanning preparations
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/72Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/84Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions otherwise than those involving only carbon-carbon unsaturated bonds
    • A61K8/89Polysiloxanes
    • A61K8/891Polysiloxanes saturated, e.g. dimethicone, phenyl trimethicone, C24-C28 methicone or stearyl dimethicone
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2800/00Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
    • A61K2800/40Chemical, physico-chemical or functional or structural properties of particular ingredients
    • A61K2800/59Mixtures
    • A61K2800/594Mixtures of polymers

Landscapes

  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Birds (AREA)
  • Epidemiology (AREA)
  • Dermatology (AREA)
  • Cosmetics (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Abstract

PURPOSE:To obtain the titled cosmetic by compounding a specific silicone polymer free from UV-absorbing effect in itself in combination with a volatile silicone oil and/or a volatile hydrocarbon oil in addition to an UV-absorber and/or UV-scattering agent. CONSTITUTION:The objective anti-suntan cosmetic having improved anti-suntan effect is produced without increasing the amount of UV-absorber and UV- scattering agent, by adding (A) one or more kinds of organic silicone polymers selected from organic silicone polymer containing two or more kinds of structural units of formula (R is 1-6C hydrocarbon group, phenyl or H) or organic silicone polymer produced by blocking the terminal of the above polymer with RSiO1/2 (the average molecular weight of the polymer is preferably 1,500-50,000), (B) a volatile hydrocarbon oil having a boiling point of <=260 deg.C under normal pressure and/or a volatile silicone oil and/or a volatile hydrocarbon oil and (C) an UV-absorber or an UV-scattering agent.

Description

【発明の詳細な説明】 [産業上の利用分野] 本発明は、日焼は防止化粧料に関する。ざらに詳しくは
、太陽光線の紫外線による皮膚の紅斑および黒化の防止
に有効であり、かつ使用性に優れた皮膚刺激の無い改良
された日焼は防止化粧料に関する。
DETAILED DESCRIPTION OF THE INVENTION [Industrial Field of Application] The present invention relates to a sunburn prevention cosmetic. More specifically, the present invention relates to an improved sun protection cosmetic that is effective in preventing skin erythema and darkening caused by ultraviolet rays of the sun, is easy to use, and does not cause skin irritation.

[従来の技術] 太陽光線の紫外線のうち、中波長紫外部の波長280〜
320 n mは、皮膚にサンパーンといわれる紅斑を
ひきおこし、甚だしくは火傷と同様な水泡を起こす。ま
た長波長紫外部の波長320〜400nmは、皮膚の黒
化をもたらし、いずれの波長も長期にわたって繰返し作
用すると皮膚の老化を促進することがわかっている。
[Conventional technology] Among the ultraviolet rays of sunlight, wavelengths of medium wavelength ultraviolet 280~
320 nm causes erythema called sampane on the skin and even causes blisters similar to burns. It is also known that long-wavelength ultraviolet wavelengths of 320 to 400 nm cause skin darkening, and that repeated effects over long periods of time accelerate skin aging.

それに対処するため、従来より中波長紫外線を吸収する
紫外線吸収剤または/および紫外線を散乱させる紫外線
散乱剤を配合した化粧料が用いられてきた。そしてより
有効な日焼防止効果を得るために紫外線吸収剤または/
および紫外線散乱剤*の配合量を増す試みが去れてきた
In order to cope with this problem, cosmetics containing ultraviolet absorbers that absorb medium-wavelength ultraviolet rays and/or ultraviolet scattering agents that scatter ultraviolet rays have been used. And to obtain more effective sun protection effect, UV absorber or/
Attempts to increase the amount of ultraviolet scattering agents* have been unsuccessful.

[発明が解決しようとする問題点] ところが、はとんどの紫外線吸収剤は皮膚刺激性を有し
ており、多量に配合した製品を繰返し塗布すると皮膚に
炎症を起こしたり、色素沈着を起こしてしまうことがあ
る。従って紫外線吸収剤を多量に配合することは紫外線
によるひぶくれや紅斑防止に対しては効果があるものの
、好ましい事ではない。
[Problems to be solved by the invention] However, most UV absorbers have skin irritation properties, and repeated application of products containing large amounts can cause skin irritation and pigmentation. Sometimes I put it away. Therefore, although it is effective to prevent blistering and erythema caused by ultraviolet rays by incorporating a large amount of ultraviolet absorber, it is not preferable.

また紫外線散乱剤を多量に配合すると、のびなどの使用
性を著しく損ない皮膚に塗布するときに均一につけられ
ずムラ焼けの原因になり好ましくない。
In addition, if a large amount of ultraviolet scattering agent is added, it is not preferable because it significantly impairs the usability such as spreadability, and when it is applied to the skin, it cannot be applied evenly and causes uneven tanning.

本発明者らは、このような事情にかんがみ、紫外線吸収
剤または/および紫外線散乱剤の配合量を増すことなく
、日焼は防止効果を増大させることを目的に鋭意研究を
重ねた結果、紫外線吸収剤または/および紫外線散乱剤
に加えて、そのもの自体は紫外線吸収効果を有しない特
定の有機シリコーン重合体を揮発性シリコーン油または
/および揮発性炭化水素油とともに化粧料中に配合する
ことにより、紫外線防止効果が著しく増大し、更に耐水
性が向上することを見出、この知見にもとづいて本発明
を完成するに至った。
In view of these circumstances, the present inventors have conducted extensive research with the aim of increasing the sunburn prevention effect without increasing the amount of UV absorbers and/or UV scattering agents. In addition to absorbers and/or ultraviolet scattering agents, by incorporating into cosmetics a specific organic silicone polymer that itself does not have an ultraviolet absorbing effect, together with volatile silicone oil and/or volatile hydrocarbon oil, It was discovered that the UV protection effect was significantly increased and the water resistance was further improved, and based on this knowledge, the present invention was completed.

[間層点を解決するための手段J すなわち本発明は、下記(A)で示される有機シリコー
ン重合体と、常圧における沸点が260℃以下の揮発性
炭化水素油または/および揮発性リコーン油または/お
よび揮発性炭化水素油と、紫外線吸収剤または/および
紫外線散乱剤とを配合してなることを特徴とする日焼は
防止化粧料を提供するものである。
[Means for solving the interlayer point J] That is, the present invention comprises an organic silicone polymer shown below (A) and a volatile hydrocarbon oil or/and volatile silicone oil having a boiling point of 260° C. or lower at normal pressure. The present invention provides a sunburn prevention cosmetic characterized by blending a volatile hydrocarbon oil and/or an ultraviolet absorber or/and an ultraviolet scattering agent.

(A)  S i 02、R31O372、R2S i
 01(Rは炭素数1〜6までの炭化水素基またはフェ
ニル基または水素を表わす)の構造単位を2種以上含む
有機シリコーン重合体、あるいはその末端をRS i 
03/2 (Rは炭素数1〜6までの炭化水素基または
フェニル基または水素を表わす)で封鎖した有機シリコ
ーン重合体からなる群から選ばれた有機シリコン重合体
の一種または二種以上。
(A) S i 02, R31O372, R2S i
An organic silicone polymer containing two or more types of structural units of 01 (R represents a hydrocarbon group having 1 to 6 carbon atoms, a phenyl group, or hydrogen), or its terminal is RS i
03/2 One or more organic silicone polymers selected from the group consisting of organic silicone polymers blocked with (R represents a hydrocarbon group having 1 to 6 carbon atoms, a phenyl group, or hydrogen).

本発明において使用される上記(A)で示きれる有機シ
リコーン重合体は、対応する既知のシラン類の加水分解
縮合によって容易に得ることができる。S s 021
 RS 103/21 R2S iOs R35i0+
/2単位の構成割合、重合度は使用目的に応じて変化さ
せることかできるが、平均分子量1500〜50000
の範囲が好ましい。例えば、SiO2単位と(CH3)
3S i 01/2単位を組み合わせれば、下記(I)
式で示されるような重合体が得られる。
The organic silicone polymer represented by (A) above used in the present invention can be easily obtained by hydrolytic condensation of corresponding known silanes. S s 021
RS 103/21 R2S iOs R35i0+
The composition ratio of /2 units and degree of polymerization can be changed depending on the purpose of use, but the average molecular weight is 1,500 to 50,000.
A range of is preferred. For example, SiO2 unit and (CH3)
If you combine 3S i 01/2 units, the following (I)
A polymer as shown in the formula is obtained.

また(CH3)2S i O単位とC5HsS i 0
3/□単位を組み合わせれば下記(II)式で示される
ような重合体が得られる。
Also, (CH3)2S i O unit and C5HsS i 0
By combining 3/□ units, a polymer as shown by the following formula (II) can be obtained.

本発明においては上記有機シリコン重合体のうちから任
意の一種または二種以上から選択されて用いられる。
In the present invention, one or more of the above organic silicone polymers may be selected and used.

本発明で用いる上記(B)の揮発性シリコーン油は例え
ば、下記(III)式あるいは下記(IV)式で表わさ
れるようなものである。
The volatile silicone oil (B) used in the present invention is, for example, one represented by the following formula (III) or (IV).

(以下余白) (II)式 (式中nは0〜3の整数を示す。) (III)式 (式中nは3〜6の整数を示す。) (m式 また本発明に用いる揮発性炭化水素油は、常圧における
沸点が260℃以下のもので、例えばアイソパー(登録
商標)A1同c1同D1同E1同″G1同H1同に1同
L1同M(エクソン社)、シェルゾール(登録商標)7
1 (シェル社)、ツルトロール(登録商標)100、
同1301同220(フィリップ社)などをあげること
ができる。
(Left space below) (II) Formula (In the formula, n represents an integer of 0 to 3.) (III) Formula (In the formula, n represents an integer of 3 to 6.) (M formula and volatile The hydrocarbon oil has a boiling point of 260°C or less at normal pressure, such as Isopar (registered trademark) A1, c1, D1, E1, "G1, H1, L1, M (Exxon), Scherzol ( Registered trademark)7
1 (Shell), Tsurutrol (registered trademark) 100,
Examples include 1301 and 220 (Philip Co.).

上記シリコン油および炭化水素油は、いずれも揮発性で
あって、かつ有機シリコーン共重合体の溶媒となりうる
Both the silicone oil and the hydrocarbon oil are volatile and can serve as a solvent for the organic silicone copolymer.

本発明においてはこれら揮発性油分のうち任意の一種ま
たは二種以上が選択されて用いられる。
In the present invention, one or more of these volatile oils may be selected and used.

本発明に使用される紫外線吸収剤および紫外線散乱剤と
しては公知の紫外線吸収剤および紫外線散乱剤が全て有
効に用いうる。当然のことながら複数の紫外線吸収剤ま
たは/および紫外線散乱剤を配合することもできる。
As the ultraviolet absorber and ultraviolet scattering agent used in the present invention, all known ultraviolet absorbers and ultraviolet scattering agents can be effectively used. Naturally, a plurality of ultraviolet absorbers and/or ultraviolet scattering agents can also be blended.

代表的な紫外線吸収剤を以下に列記する。Representative ultraviolet absorbers are listed below.

安、@香酸系のものとして、 バラアミノ安息香酸(以下PABAと略す)グリセリル
PABA エチルジヒドロキシプロビルPABA N−エトキシレートPABAエチルエーテルN−ジメチ
ルPABAエチルエーテル N−ジメチルPABAブチルエーテル N−ジメチルPABAアミルエーテル オクチルジメチルPABA アントラニリック酸系のものとして、 ホモメンチル−N−アセチルアントラニレートサルチル
酸系のものとして、 アミルサリシレート メンチルサリシレート オクチルサリシレート フェニルサリシレート ペンジルサリシレート P−イソブロバノールフェニルサリシレート桂皮酸系の
ものとして、 オクチルシンナメート エチル−4−イソプロピルシンナメートエチル−2,4
−ジイソブ口ビルシンナメートメチル−2,4−ジイソ
プロピルシンナメートプロピル−P−メトキシシンナメ
ート イソプロビル−P−メトキシシンナメートイソアミル−
P−メトキシシンナメートオクチルメトキシシンナメー
ト 2−エトキシエチル−P−メトキシシンナメート シクロへキシル−P−メトキシシンナメートエチル−α
−シアノ−β−フェニルシンナメート 2−エチルへキシル−α−シアノ−β−フェニルシンナ
メート グリセリルモノ−2−エチルヘキサノイルージパラメト
キシシンナメート ベンゾフェノン系のものとして 2.4−ジヒドロキシベンゾフェノン 2.2°−ジヒドロキシ−4−メトキシベンゾフェノン 2.2゛−ジヒドロキシ−4,4′ジメトキシベンゾフ
エノン 2.2’、4.4’−テトラヒドロキシベンゾフェノン 2−ヒドロキシ−4−メトキシベンゾフェノン2−ヒド
ロキシ−4−メトキシ−4′−メチルベンゾフェノン 4−フェニルベンゾフェノン 2−エチルへキシル−4′−フェニル−ベンゾフェノン
−2−カルボキシレート 2−ヒドロキシ−4−n−オクトキシベンゾフェノン 4−ヒドロキシ−3−カルボキシベンゾフェノン その他のものとして、 3−(4°−メチルベンジリデン)−d、l−カンファ
ー 3−ベンジリデン−d、l−カンフ− ウロカニン酸 ウロカニン酸エチルエステル 2−フェニル−5−メチルベンゾキサゾール2.2′−
ヒドロキシ−5−メチルフェニル−ベンゾトリアゾール 2−(2’−ヒドロキシ−5−t−オク≠ルフェニル)
−ベンゾトリアゾール ジベンザラジン ジベンゾイルメタン 4−メトキシ−4°−t−ブチル−ジベンゾイルメタン 5−(3,3−ジメチル−2−ノルボルニリデン)−3
−ペンタン−2−オン カルコン誘導体 などがあげられる。
As aromatic acid-based ones, aminobenzoic acid (hereinafter abbreviated as PABA) glyceryl PABA ethyldihydroxypropyl PABA N-ethoxylate PABA ethyl ether N-dimethyl PABA ethyl ether N-dimethyl PABA butyl ether N-dimethyl PABA amyl ether Octyldimethyl PABA As an anthranilic acid type, Homomenthyl-N-acetylanthranilate as a salicylic acid type, Amyl salicylate Menthyl salicylate Octyl salicylate Phenyl salicylate Penzyl salicylate P-Isobrobanol Phenyl salicylate As a cinnamic acid type , Octyl cinnamate ethyl-4-isopropyl cinnamate ethyl-2,4
-Diisobuvircinnamate methyl -2,4-diisopropylcinnamatepropyl -P-methoxycinnamateisoprovil -P-methoxycinnamateisoamyl-
P-methoxycinnamate octyl methoxycinnamate 2-ethoxyethyl-P-methoxycinnamate cyclohexyl-P-methoxycinnamate ethyl-α
-Cyano-β-phenylcinnamate 2-ethylhexyl-α-cyano-β-phenylcinnamate glyceryl mono-2-ethylhexanoyl diparamethoxycinnamate As a benzophenone type 2.4-dihydroxybenzophenone 2.2 °-dihydroxy-4-methoxybenzophenone 2.2'-dihydroxy-4,4'dimethoxybenzophenone 2.2',4.4'-tetrahydroxybenzophenone 2-hydroxy-4-methoxybenzophenone 2-hydroxy-4- Methoxy-4'-methylbenzophenone 4-phenylbenzophenone 2-ethylhexyl-4'-phenyl-benzophenone-2-carboxylate 2-hydroxy-4-n-octoxybenzophenone 4-hydroxy-3-carboxybenzophenone Others as 3-(4°-methylbenzylidene)-d,l-camphor 3-benzylidene-d,l-camphor-urocanic acid urocanic acid ethyl ester 2-phenyl-5-methylbenzoxazole 2.2'-
Hydroxy-5-methylphenyl-benzotriazole 2-(2'-hydroxy-5-t-oc≠ruphenyl)
-benzotriazoledibenzalazinedibenzoylmethane 4-methoxy-4°-t-butyl-dibenzoylmethane 5-(3,3-dimethyl-2-norbornylidene)-3
-pentan-2-one chalcone derivatives and the like.

また代表的な紫外線散乱剤としては以下のようなものを
あげることができる。
Moreover, the following can be mentioned as typical ultraviolet scattering agents.

酸化チタン 微粒子酸化チタン 酸化亜鉛 酸化鉄 微粒子酸化鉄 本発明の化粧料のタイプは任意であり、オイル、ローシ
ョン、乳液、クリーム、油性スティック、油性ファンデ
ーション等のいずれの製品タイプも可能である。
Fine particles of titanium oxide Titanium oxide Zinc iron oxide Fine particles of iron oxide The type of the cosmetic of the present invention is arbitrary, and any product type such as oil, lotion, milky lotion, cream, oily stick, oily foundation, etc. is possible.

必須構成成分の適正な配合割合は、 次のとおりである
The appropriate mixing ratio of the essential components is as follows.

すなわち目的とする製品タイプにより異なるが、有機シ
リコーン重合体は、日焼は防止化粧料全量中の1〜Hw
t%、揮発性シリコーン油または/および揮発性炭化水
素油は1〜99wt%である。揮発性シリコーン油又は
/および揮発性炭化水素油が多いと溶液状を呈し、有機
シリコーン重合体が増量するにしたがって固型状になる
In other words, although it differs depending on the intended product type, organic silicone polymers account for 1 to 1 Hw of the total amount of sunburn prevention cosmetics.
t%, volatile silicone oil or/and volatile hydrocarbon oil is 1 to 99 wt%. When the amount of volatile silicone oil and/or volatile hydrocarbon oil is large, it takes on the form of a solution, and as the amount of the organic silicone polymer increases, it becomes solid.

また紫外線吸収剤または/および紫外線散乱剤の配合量
および組合せは求める日焼は防止効果に応じて決定され
るが、日焼は防止効果を考慮すると0.005w t%
以上必要である。上限は使用性や皮膚安全性の面から個
々に異なるが、例えばホモメンチルサリシレートでは1
5wt%、オクチルメチルPABAは8wt%、酸化チ
タンは80%である。
In addition, the amount and combination of UV absorbers and/or UV scattering agents are determined depending on the desired sunburn prevention effect, but considering the sunburn prevention effect, it is 0.005wt%.
The above is necessary. The upper limit varies depending on the usability and skin safety, but for example, for homomenthyl salicylate, 1
5 wt%, octyl methyl PABA is 8 wt%, and titanium oxide is 80%.

本発明の日焼は防止化粧料には上記の他に、目的に応じ
て本発明の効果を損なわない量的、質的範囲内で、ざら
に油脂類、ロウ類、薬剤、体質顔料、着色顔料、可塑剤
、香料あるいは他の揮発性成分等を配合しても良い。
In addition to the above, the sunburn prevention cosmetics of the present invention may include, depending on the purpose, oils and fats, waxes, drugs, extender pigments, and colorings within a quantitative and qualitative range that does not impair the effects of the present invention. Pigments, plasticizers, fragrances, or other volatile components may also be added.

[実施例] 以下、実施例により本発明をざらに詳細に説明する。本
発明は、これらによって限定されるものではない。配合
量は全てwt%である。
[Example] Hereinafter, the present invention will be explained in detail with reference to Examples. The present invention is not limited by these. All blending amounts are wt%.

実施例1 サンスクリーンオイル 1) ジメチルシロキサン 1cs(n=1)10.0
2) ジメチルシロキサン 2cs (n=3)  1
3.03) 有機シリコーン重合体*65 、04) 
グリセリルトリイソステアレート10.05) オクチ
ルジメチルP A B A     2.0*(C)1
3)3si0□72単位’ (CsHshSiO単位:
(CH3)5i03z。単位:sio。単位=0.9:
O,C0,2:1で平均分子量約2000である有機シ
リコーン。
Example 1 Sunscreen oil 1) Dimethylsiloxane 1cs (n=1) 10.0
2) Dimethylsiloxane 2cs (n=3) 1
3.03) Organic silicone polymer *65, 04)
Glyceryl triisostearate 10.05) Octyldimethyl P A B A 2.0*(C)1
3) 3si0□72 units' (CsHshSiO units:
(CH3)5i03z. Unit: sio. Unit = 0.9:
An organosilicone with an O,C0,2:1 ratio and an average molecular weight of about 2000.

80℃で5を4に溶解し、冷却したものを1〜3を攪拌
溶解した溶液に混合し容器に充填してサンスクリーンオ
イルを得た。
5 was dissolved in 4 at 80°C, and the cooled mixture was mixed with a solution obtained by stirring and dissolving 1 to 3, and the mixture was filled into a container to obtain a sunscreen oil.

比較例1 サンスクリーンオイル 実施例1の1〜3をグリセリルトリイソステアレートに
おきかえたもの。
Comparative Example 1 Sunscreen oil in which 1 to 3 of Example 1 were replaced with glyceryl triisostearate.

実施例2 油性ファンデーション 1) カオリン           25.。Example 2 Oil-based foundation 1) Kaolin 25. .

2) 微粒子酸化チタン        15.03)
 酸化鉄             3.04) マイ
クロクリスタリンワックス  4.05) 流動パラフ
ィン         5.06) ソルビタンセスキ
オレート    1.07) 有機シリコーン重合体*
2.。
2) Fine particle titanium oxide 15.03)
Iron oxide 3.04) Microcrystalline wax 4.05) Liquid paraffin 5.06) Sorbitan sesquiolate 1.07) Organic silicone polymer*
2. .

8) アイソパー(登録商標) G    45.09
) 香料             適量10)酸化防
止剤            適量” (CH3hSi
0172単位:5i02単位=1.5:1テ平均分子量
約4000の有機シリコーン。
8) Isopar (registered trademark) G 45.09
) Fragrance: Appropriate amount 10) Antioxidant: Appropriate amount” (CH3hSi
0172 units: 5i02 units = 1.5:1 Organic silicone with an average molecular weight of about 4000.

4〜8および10を70℃〜80℃ で攪拌溶解した後
、1〜3を加えて分散する。脱気後9を加えて所定の容
器に充填して油性ファンデーションを得た。
After stirring and dissolving 4 to 8 and 10 at 70°C to 80°C, 1 to 3 are added and dispersed. After degassing, 9 was added and filled into a predetermined container to obtain an oil-based foundation.

比較例2 油性ファンデーション 実施例2の7〜8を流動パラフィンに置き換えたもの。Comparative Example 2 Oil-based foundation Example 2, except that 7 and 8 were replaced with liquid paraffin.

実施例3 日焼は止め乳液 1) 環状ジメチルシロキサン(n=5)  10.0
2) 有機シリコーン重合体*20 、03) 流動パ
ラフィン         4.04) ソルビタンジ
イソステアレート 3.05) ポリオキシアルキレン
変性 オルガノポリシロキサン 3.0 6) イオン交換水         47.07) 
グリセリン          3.08) 微粒子酸
化鉄         5.09) オクチルジメチル
PABA    2.010)4−メトキシ−4°−t −ブチルージベンゾイルメタン  2.011)  防
腐剤             適量12)  酸化防
止剤          適量13)  香料    
          適量*(CH3)3si01/2
単位:5i02単位=0.8:Iテ平均分子量約100
00の有機シリコーン 1〜5および9.10.12.13を70℃で攪拌溶解
し、これに8を分散する。これにあらがしめ70℃で溶
解した6、7.11、を添加し、乳化分散後冷却して目
的の乳液を得た。
Example 3 Sunscreen emulsion 1) Cyclic dimethylsiloxane (n=5) 10.0
2) Organic silicone polymer *20, 03) Liquid paraffin 4.04) Sorbitan diisostearate 3.05) Polyoxyalkylene-modified organopolysiloxane 3.0 6) Ion-exchanged water 47.07)
Glycerin 3.08) Particulate iron oxide 5.09) Octyldimethyl PABA 2.010) 4-methoxy-4°-t-butyl-dibenzoylmethane 2.011) Preservative appropriate amount 12) Antioxidant appropriate amount 13) Fragrance
Appropriate amount*(CH3)3si01/2
Unit: 5i02 unit = 0.8: Ite average molecular weight approximately 100
Organic silicones 1 to 5 and 9.10.12.13 of 00 are stirred and dissolved at 70°C, and 8 is dispersed therein. 6, 7.11, which had been mixed and dissolved at 70°C, were added to this, and after emulsification and dispersion, the mixture was cooled to obtain the desired emulsion.

比較例3 日焼は止め乳液 実施例3の1および2を流動パラフィンに置き換えたも
の。
Comparative Example 3 A sunscreen emulsion in which 1 and 2 of Example 3 were replaced with liquid paraffin.

実施例4 化粧下地 1) ジメチルシロキサン2cs(n=3)   14
.02) 有機シリコーン重合体*5.。
Example 4 Makeup base 1) Dimethylsiloxane 2cs (n=3) 14
.. 02) Organic silicone polymer *5. .

3) グリセリルトリイソステアレート10.04) 
アイソパー(登録商標) G     5.05) ソ
ルビタンセスキオレート    1.06) ポリオキ
シアルキレン 変性オルガノポリシロキサン    3.07) イオ
ン交換水         45.08)   1.3
ブチレングリコール    5.09) 微粒子酸化チ
タン       10.010)  オクチルジメチ
ルP A B A     2.011)  防腐剤 
           適量12)  酸化防止剤  
        適量13)  香料        
     適量::: (CH3)+SiO単位: C
6H55i0273単位=1:0.5で平均分子量約5
0000の有機シリコーン。
3) Glyceryl triisostearate 10.04)
Isopar (registered trademark) G 5.05) Sorbitan sesquiolate 1.06) Polyoxyalkylene-modified organopolysiloxane 3.07) Ion-exchanged water 45.08) 1.3
Butylene glycol 5.09) Particulate titanium oxide 10.010) Octyldimethyl P A B A 2.011) Preservative
Appropriate amount 12) Antioxidant
Appropriate amount 13) Fragrance
Appropriate amount::: (CH3)+SiO unit: C
6H55i0273 units = 1:0.5, average molecular weight approximately 5
0000 organic silicone.

1〜6および10.12.13を70℃で攪拌溶解し、
これにあらかじめ70℃で溶解した7、8.12を添加
し、乳化分散後冷却して目的の化粧下地を得た。
1 to 6 and 10.12.13 were stirred and dissolved at 70°C,
7 and 8.12, which had been previously dissolved at 70°C, were added to this, and after emulsification and dispersion, the mixture was cooled to obtain the desired makeup base.

実施例5 液状頬紅 1) メチルフェニルポリシロキサン 10.02) 
デカメチルシクロペンタ シロキサン           49.03) 固型
パラフィン         4.04) マイクロク
リスタリンワックス 3.05) ソルビタンセスキオ
レート1.06) 有機シリコーン重合体*30 、0
7) マイカ            15.。
Example 5 Liquid blusher 1) Methylphenylpolysiloxane 10.02)
Decamethylcyclopentasiloxane 49.03) Solid paraffin 4.04) Microcrystalline wax 3.05) Sorbitan sesquiolate 1.06) Organic silicone polymer *30, 0
7) Mica 15. .

8) 二酸化チタン         2.09) 酸
化鉄            2.010)  赤色2
26号         1.011)  オクチルジ
メチルPABA    1.012)4−メトキシ−4
°−t−ブチル−ジベンゾイルメタン       1
.013)  酸化防止剤          適量1
4)  香料             適量* (C
H3)3siot/z単位’ (CH3) 2siO単
位:(CL)Si03/2単位:5i02単位=0.6
:0.1:0.2:0.7で平均分子量約1500であ
る有機シリコーン。
8) Titanium dioxide 2.09) Iron oxide 2.010) Red 2
No. 26 1.011) Octyldimethyl PABA 1.012) 4-methoxy-4
°-t-Butyl-dibenzoylmethane 1
.. 013) Antioxidant appropriate amount 1
4) Appropriate amount of fragrance* (C
H3) 3siot/z unit' (CH3) 2siO unit: (CL) Si03/2 unit: 5i02 unit = 0.6
:0.1:0.2:0.7 and has an average molecular weight of about 1500.

1〜6および11〜13を70〜80℃で混合溶解する
。別に7〜10を混合粉砕する。両者を攪拌混合し、脱
気後、14を加えて液状頬紅を得た。
1 to 6 and 11 to 13 are mixed and dissolved at 70 to 80°C. Separately, mix and grind 7 to 10. Both were stirred and mixed, and after degassing, 14 was added to obtain a liquid blusher.

上記の実施例3例および比較例3例を動物を用いたSP
F測定法にて日焼は防止効果を評価した。
The above three examples and three comparative examples were subjected to SP using animals.
The sunburn prevention effect was evaluated using the F measurement method.

すなわち背部毛を脱毛クリームにて除去したモルーモッ
トに、試料を2μl/cm2になるよう塗布する。15
分後に東芝FL−3Eランプ12灯で紫外線を照射した
。照射後24時間経過した時点で試料塗布部および試料
無塗布部の紅斑を観察し、かすかな紅斑を起こすのに要
した最少の紫外線量を求める。求めた最少紫外線量から
下式に従ってS P F (Sun Protecti
on Factor)を計算する〇結果を表1に示す。
That is, a sample is applied to a guinea pig whose back hair has been removed using a hair removal cream at a concentration of 2 μl/cm 2 . 15
After a few minutes, ultraviolet rays were irradiated using 12 Toshiba FL-3E lamps. 24 hours after irradiation, observe the erythema on the sample-applied area and the sample-unapplied area, and determine the minimum amount of ultraviolet rays required to cause faint erythema. From the obtained minimum amount of ultraviolet rays, calculate S P F (Sun Protecti) according to the formula below.
on Factor) The results are shown in Table 1.

(以下余白) 塗布部皮膚に紅斑を 表1 本実験の結果から、紫外線吸収剤または/および紫外線
散乱剤とともに有機シリコーン重合体と、揮発性シリコ
ーン油または/および揮発性炭化水素油を配合した実施
例は比較例と比較して、非常に紫外線防止効果の増大す
ることが実証された。
(Margins below) Table 1: Erythema on the skin at the application site Table 1 Based on the results of this experiment, it was found that an organic silicone polymer and a volatile silicone oil or/and a volatile hydrocarbon oil were blended together with a UV absorber or/and a UV scattering agent. It was demonstrated that the example has a significantly increased UV protection effect compared to the comparative example.

更に実施例1.2.3.4.5につき、8月に当社研究
所(横浜港北区)屋上にて実使用テストをおこなった。
Furthermore, practical use tests were conducted for Examples 1, 2, 3, 4, and 5 on the roof of our laboratory (Kohoku Ward, Yokohama) in August.

試験項目は、日焼は防止効果に加えて、長波長紫外線に
より引き起こされる一次黒化防止効果を検討した。
In addition to the sunburn prevention effect, the test items examined the primary blackening prevention effect caused by long wavelength ultraviolet rays.

その結果、これら5例を使用した各群は、高い日焼は防
止効果を示すばかりでなく、−大黒化の抑制が有意に認
められた。
As a result, each group using these five cases not only showed an effect of preventing high sunburn, but also significantly suppressed darkening.

また皮膚に塗布した時にムラにならず非常に使用性も向
上した。
Furthermore, when applied to the skin, it did not become uneven and the usability was greatly improved.

[発明の効果] 本発明の日焼は防止化粧料は、日焼けを防止する効果に
優れ、皮膚に対する安全性や使用感触も良好で、ムラ焼
けなどの問題もない化粧料である。
[Effects of the Invention] The sunburn prevention cosmetic of the present invention has an excellent sunburn prevention effect, is safe to the skin, has a good feel when used, and is free from problems such as uneven tanning.

Claims (1)

【特許請求の範囲】[Claims] (1)下記(A)で示される有機シリコーン重合体と、
常圧における沸点が260℃以下の揮発性炭化水素油ま
たは/および揮発性シリコーン油または/および揮発性
炭化水素油と、紫外線吸収剤または/および紫外線散乱
剤とを配合してなることを特徴とする日焼け防止化粧料
。 (A)SiO_2、RSiO_3_/_2、R_2Si
O、(Rは炭素数1〜6までの炭化水素基また はフェニル基または水素を表わす)の構 造単位を2種以上含む有機シリコーン重 合体、あるいはその末端をRSiO_3_/_2(Rは
炭素数1〜6までの炭化水素基また はフェニル基または水素を表わす)で封 鎖した有機シリコーン重合体からなる群 から選ばれた有機シリコン重合体の一種 または二種以上。
(1) An organic silicone polymer represented by (A) below,
It is characterized by being made by blending a volatile hydrocarbon oil or/and a volatile silicone oil or/and a volatile hydrocarbon oil with a boiling point of 260°C or less at normal pressure, and an ultraviolet absorber or/and an ultraviolet scattering agent. Sun protection cosmetics. (A) SiO_2, RSiO_3_/_2, R_2Si
O, (R represents a hydrocarbon group having 1 to 6 carbon atoms, a phenyl group, or hydrogen), or an organic silicone polymer containing two or more structural units of One or more organosilicon polymers selected from the group consisting of organosilicon polymers blocked with up to 6 hydrocarbon groups or phenyl groups or hydrogen.
JP61075774A 1986-04-02 1986-04-02 Sun protection cosmetics Expired - Fee Related JPH0811723B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP61075774A JPH0811723B2 (en) 1986-04-02 1986-04-02 Sun protection cosmetics

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP61075774A JPH0811723B2 (en) 1986-04-02 1986-04-02 Sun protection cosmetics

Publications (2)

Publication Number Publication Date
JPS62234012A true JPS62234012A (en) 1987-10-14
JPH0811723B2 JPH0811723B2 (en) 1996-02-07

Family

ID=13585889

Family Applications (1)

Application Number Title Priority Date Filing Date
JP61075774A Expired - Fee Related JPH0811723B2 (en) 1986-04-02 1986-04-02 Sun protection cosmetics

Country Status (1)

Country Link
JP (1) JPH0811723B2 (en)

Cited By (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2622441A1 (en) * 1987-10-28 1989-05-05 Oreal TRANSPARENT COSMETIC COMPOSITION REFLECTING INFRARED RADIATION AND ITS USE FOR THE PROTECTION OF THE HUMAN SKIN AGAINST INFRARED RADIATION
FR2646346A1 (en) * 1989-04-26 1990-11-02 Thorel Jean Composition for the topical deposition of a permeable and light-reflecting continuous film
EP0431821A2 (en) * 1989-12-05 1991-06-12 Dow Corning Corporation Sunscreen formulation containing a phenyl functional organosilicon compound
US5246694A (en) * 1990-07-23 1993-09-21 Chesebrough-Pond's Usa Co., Division Of Conopco, Inc. Shampoo composition
US5676938A (en) * 1992-09-29 1997-10-14 Toshiba Silicone Co., Ltd. Cosmetic composition
US6991782B2 (en) 2000-06-19 2006-01-31 L'oréal Cosmetic compositions comprising at least one polymethylsilsesquioxane film former
JP2008537952A (en) * 2005-04-14 2008-10-02 モーメンティブ・パフォーマンス・マテリアルズ・インク Silicone resin-containing personal care composition having good characteristics, its production method and use thereof
WO2009136486A1 (en) 2008-05-08 2009-11-12 モメンティブ・パフォーマンス・マテリアルズ・ジャパン合同会社 Cosmetic
WO2011081218A1 (en) 2009-12-28 2011-07-07 Dow Corning Toray Co., Ltd. Phenyl-containing organopolysiloxane composition, raw cosmetic material, and glossy cosmetic material
WO2013161429A1 (en) 2012-04-23 2013-10-31 Dow Corning Toray Co., Ltd. Liquid aryl group-containing polyorganosiloxane
US10765619B2 (en) 2018-06-04 2020-09-08 Shin-Etsu Chemical Co., Ltd. Silicone resin, making method, and cosmetics
WO2021171735A1 (en) 2020-02-27 2021-09-02 信越化学工業株式会社 Cosmetic
WO2021201031A1 (en) * 2020-03-31 2021-10-07 株式会社コーセー Oil-based cosmetic
WO2022172567A1 (en) 2021-02-10 2022-08-18 信越化学工業株式会社 Emulsified composition and cosmetic

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS59254A (en) * 1982-06-25 1984-01-05 Fujitsu Ltd Simultaneous multiple address data transfer controlling system to plural terminals connected to same circuit
JPS6160605A (en) * 1984-08-30 1986-03-28 Shiseido Co Ltd Cosmetic

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS59254A (en) * 1982-06-25 1984-01-05 Fujitsu Ltd Simultaneous multiple address data transfer controlling system to plural terminals connected to same circuit
JPS6160605A (en) * 1984-08-30 1986-03-28 Shiseido Co Ltd Cosmetic

Cited By (20)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2622441A1 (en) * 1987-10-28 1989-05-05 Oreal TRANSPARENT COSMETIC COMPOSITION REFLECTING INFRARED RADIATION AND ITS USE FOR THE PROTECTION OF THE HUMAN SKIN AGAINST INFRARED RADIATION
BE1003842A5 (en) * 1987-10-28 1992-06-30 Oreal Cosmetic reflecting the infrared transparent and use for the protection of human skin against infrared.
FR2646346A1 (en) * 1989-04-26 1990-11-02 Thorel Jean Composition for the topical deposition of a permeable and light-reflecting continuous film
EP0431821A2 (en) * 1989-12-05 1991-06-12 Dow Corning Corporation Sunscreen formulation containing a phenyl functional organosilicon compound
US5246694A (en) * 1990-07-23 1993-09-21 Chesebrough-Pond's Usa Co., Division Of Conopco, Inc. Shampoo composition
US5676938A (en) * 1992-09-29 1997-10-14 Toshiba Silicone Co., Ltd. Cosmetic composition
US6991782B2 (en) 2000-06-19 2006-01-31 L'oréal Cosmetic compositions comprising at least one polymethylsilsesquioxane film former
JP2008537952A (en) * 2005-04-14 2008-10-02 モーメンティブ・パフォーマンス・マテリアルズ・インク Silicone resin-containing personal care composition having good characteristics, its production method and use thereof
US8329153B2 (en) 2008-05-08 2012-12-11 Momentive Performance Materials Japan Llc Cosmetic product
WO2009136486A1 (en) 2008-05-08 2009-11-12 モメンティブ・パフォーマンス・マテリアルズ・ジャパン合同会社 Cosmetic
EP2730276A2 (en) 2008-05-08 2014-05-14 Momentive Performance Materials Japan LLC Cosmetic product
WO2011081218A1 (en) 2009-12-28 2011-07-07 Dow Corning Toray Co., Ltd. Phenyl-containing organopolysiloxane composition, raw cosmetic material, and glossy cosmetic material
WO2013161429A1 (en) 2012-04-23 2013-10-31 Dow Corning Toray Co., Ltd. Liquid aryl group-containing polyorganosiloxane
US9415001B2 (en) 2012-04-23 2016-08-16 Dow Corning Toray Co., Ltd. Liquid aryl group-containing polyorganosiloxane
US10765619B2 (en) 2018-06-04 2020-09-08 Shin-Etsu Chemical Co., Ltd. Silicone resin, making method, and cosmetics
US11033481B2 (en) 2018-06-04 2021-06-15 Shin-Etsu Chemical Co., Ltd. Silicone resin, making method, and cosmetics
WO2021171735A1 (en) 2020-02-27 2021-09-02 信越化学工業株式会社 Cosmetic
WO2021201031A1 (en) * 2020-03-31 2021-10-07 株式会社コーセー Oil-based cosmetic
WO2022172567A1 (en) 2021-02-10 2022-08-18 信越化学工業株式会社 Emulsified composition and cosmetic
KR20230137352A (en) 2021-02-10 2023-10-04 신에쓰 가가꾸 고교 가부시끼가이샤 Emulsion compositions and cosmetics

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