JPH0623374B2 - Gel composition containing CFC - Google Patents

Gel composition containing CFC

Info

Publication number
JPH0623374B2
JPH0623374B2 JP6017885A JP6017885A JPH0623374B2 JP H0623374 B2 JPH0623374 B2 JP H0623374B2 JP 6017885 A JP6017885 A JP 6017885A JP 6017885 A JP6017885 A JP 6017885A JP H0623374 B2 JPH0623374 B2 JP H0623374B2
Authority
JP
Japan
Prior art keywords
weight
polyoxyalkylene
gel composition
modified
present
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 - Lifetime
Application number
JP6017885A
Other languages
Japanese (ja)
Other versions
JPS61218677A (en
Inventor
正昭 石渡
裕 奥貫
富幸 難波
▲吉▼宏 木村
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 JP6017885A priority Critical patent/JPH0623374B2/en
Publication of JPS61218677A publication Critical patent/JPS61218677A/en
Publication of JPH0623374B2 publication Critical patent/JPH0623374B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • 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
    • A61K8/19Cosmetics or similar toiletry preparations characterised by the composition containing inorganic ingredients
    • A61K8/26Aluminium; Compounds thereof
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/02Cosmetics or similar toiletry preparations characterised by special physical form
    • A61K8/04Dispersions; Emulsions
    • A61K8/042Gels
    • 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
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/40Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
    • A61K8/41Amines
    • A61K8/416Quaternary ammonium compounds
    • 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
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/69Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing fluorine
    • 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
    • A61K8/894Polysiloxanes saturated, e.g. dimethicone, phenyl trimethicone, C24-C28 methicone or stearyl dimethicone modified by a polyoxyalkylene group, e.g. cetyl dimethicone copolyol
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q19/00Preparations for care of the skin

Description

【発明の詳細な説明】 〔産業上の利用分野〕 本発明は安定性、使用性に優れるフロンを含むゲル組成
物に関する。
DETAILED DESCRIPTION OF THE INVENTION [Industrial field of use] The present invention relates to a gel composition containing chlorofluorocarbon having excellent stability and usability.

〔従来の技術〕[Conventional technology]

従来、フロンはエアゾール製品の噴射剤としての用途が
ほとんどであり、それには常温で気体のものが主に用い
られてきた。常温で液状のフロンはほとんど利用されて
いない。
Conventionally, CFCs have been mostly used as a propellant for aerosol products, and those that are gaseous at room temperature have been mainly used. CFCs that are liquid at room temperature are rarely used.

化学的に安定で皮膚安全生の高い常温で液状のフロン
を、たとえば、夏用のメーキャップ化粧料に配合すれ
ば、乾きが速くて化粧もちの優れた、しかも清涼感を有
するといった効果が期待できる。
When chemical-stable and safe skin-friendly CFCs, which are liquid at room temperature, are blended with, for example, makeup cosmetics for summer, it can be expected to have the effects of quick drying, excellent makeup lasting, and a refreshing feeling. .

また、他の揮発性油分、たとえば、低重合度の環情ジメ
チルポリシロキサン、鎖状ジメチルポリシロキサンやイ
ソパラフィンを利用した製品中にフロンを併用すれば、
揮発速度が自由に調節できるようになり、製品処方の幅
を非常に広げることができる。
Also, if chlorofluorocarbon is used in combination with other volatile oil components, for example, products using low polymerization degree cyclic dimethyl polysiloxane, chain dimethyl polysiloxane or isoparaffin,
The volatilization rate can be adjusted freely, and the range of product formulations can be greatly expanded.

〔発明が解決しようとする問題点〕[Problems to be solved by the invention]

しかしながら、上記のような効果が期待できるにもかか
わらず、フロンが利用されることがなかったのは、フロ
ンの増粘安定化が非常に難しかったからに他ならない。
これまで、常温で液状のフロンを安定に配合した例は皆
無である。
However, despite the above-mentioned effects being expected, chlorofluorocarbon has never been used because it is very difficult to stabilize the viscosity of chlorofluorocarbon.
Until now, there have been no examples of stably mixing liquid CFCs at room temperature.

〔問題点を解決するための手段〕[Means for solving problems]

本発明者らは、こうした事情にかんがみ、フロン、とく
に常温で液状のフロンの増粘法について鋭意研究を重ね
た結果、フロンに特定のシリコン化合物と有機変性粘土
鉱物と水とを特定量配合することにより、任意の粘度を
有する経時安定性及び使用性が良好なゲル組成物が得ら
れることを見出し、この知見に基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 intensive studies on a method for thickening freon, especially freon which is liquid at room temperature, and as a result, blended freon with a specific amount of a specific silicon compound, an organically modified clay mineral and water. As a result, it was found that a gel composition having an arbitrary viscosity and good temporal stability and usability can be obtained, and the present invention has been completed based on this finding.

すなわち、本発明は、フロン、一般式(I)、(II)ま
たは(III)で示されるポリオキシアルキレン変性オル
ガノポリシロキサンの一種または二種以上、有機変性粘
土鉱物ならびに水を配合することを特徴とするフロンを
含むゲル組成物を提供するものである。
That is, the present invention is characterized by blending CFCs, one or more polyoxyalkylene-modified organopolysiloxanes represented by the general formula (I), (II) or (III), an organically modified clay mineral and water. And a gel composition containing chlorofluorocarbon.

{一般式(I)、(II)、(III)中、Rはメチル基ま
たは一部がフェニル基、R′は水素または炭素数1〜12
のアルキル基、pは1〜5の数、qは2〜3数、x、
m、nは平均数でポリオキシアルキレン変性オルガノポ
リシロキサンが分子中にポリオキシアルキレン基を2〜
40重量%含有し且つ該ポリオキシアルキレン変性オルガ
ノポリシロキサンの粘度が25℃において5〜3000セン
チストークスになるような数値を表す。} 以下、本発明の構成について詳述する。
{In the general formulas (I), (II) and (III), R is a methyl group or a part thereof is a phenyl group, R'is hydrogen or a carbon number of 1 to 12
Alkyl group, p is a number from 1 to 5, q is a number from 2 to 3, x,
m and n are average numbers, and the polyoxyalkylene-modified organopolysiloxane has 2 to 2 polyoxyalkylene groups in the molecule.
The content is 40% by weight and represents a value such that the viscosity of the polyoxyalkylene-modified organopolysiloxane is 5 to 3000 centistokes at 25 ° C. } Hereinafter, the configuration of the present invention will be described in detail.

本発明で用いられるフロンは従来用いられている周知の
ものを使用することができる。たとえば、ジクロルモノ
フルオルメタン、トリクロルモノフルオルメタン、テト
ラクロルジフルオルエタン、トリクロルトリフルオルエ
タン、ジブロムテトラフルオルエタンなどが挙げられ
る。これらの中から一種又は二種以上が任意に選択され
る。
As the CFC used in the present invention, a conventionally known CFC can be used. Examples thereof include dichloromonofluoromethane, trichloromonofluoromethane, tetrachlorodifluoroethane, trichlorotrifluoroethane, and dibromotetrafluoroethane. One kind or two kinds or more are arbitrarily selected from these.

配合量は通常本発明の組成物全量中の1〜90重量%であ
る。
The compounding amount is usually 1 to 90% by weight based on the total amount of the composition of the present invention.

本発明で用いられるポリオキシアルキレン変性オルガノ
ポリシロキサン(以下、ポリエーテル変性シリコンと略
記する)は前記一般式(I)、(II)または(III)で
表されるものであり、これらのうちの任意の一種又は二
種以上が選ばれて用いられる。
The polyoxyalkylene-modified organopolysiloxane (hereinafter abbreviated as polyether-modified silicon) used in the present invention is represented by the above general formula (I), (II) or (III). Any one kind or two or more kinds are selected and used.

本発明の目的に合致した効果、すなわち経時安定性及び
使用性の良好なフロン増粘効果を満足せしめるために
は、ポリエーテル変性シリコンはポリオキシアルキレン
基をその分子量に対して2〜40重量%の割合で含有し且
つ25℃においてそのもの自体の粘度が5〜3000センチス
ドークスの範囲に存する必要がある。すなわち、ポリオ
キシアルキレン基のポリエーテル変性シリコン全重量に
対する割合が2重量%未満では増粘効果が十分でなく、
40重量%を越えると、経時安定性が悪くなる。またポリ
エーテル変性シリコンの粘度が5センチストークス未満
では増粘効果が十分でなく、3000センチストークスを越
えると使用感がべたつき好ましくない。
In order to satisfy the effect consistent with the object of the present invention, that is, the chlorofluorocarbon thickening effect with good stability and usability, the polyether-modified silicone has a polyoxyalkylene group of 2 to 40% by weight based on its molecular weight. It is necessary to contain it in a ratio of 5 and a viscosity of itself at 25 ° C. in the range of 5 to 3000 centigrade. That is, when the ratio of the polyoxyalkylene group to the total weight of the polyether-modified silicon is less than 2% by weight, the thickening effect is not sufficient,
If it exceeds 40% by weight, the stability with time deteriorates. If the viscosity of the polyether-modified silicone is less than 5 centistokes, the thickening effect is not sufficient, and if it exceeds 3000 centistokes, the feeling of use becomes sticky and it is not preferable.

本発明のゲル組成物に対するポルエーテル変性シリコン
の配合量は全量中の 0.1から30重量%の範囲で選択され
るが、好ましくは 0.2〜25重量%である。 0.1重量%未
満では増粘効果が十分でなく経時安定性も悪い。30重量
%を越えるとべたつきが感じられ、また化粧もちも悪く
なる。
The amount of the polyether-modified silicone compounded in the gel composition of the present invention is selected in the range of 0.1 to 30% by weight, preferably 0.2 to 25% by weight. If it is less than 0.1% by weight, the thickening effect is insufficient and the stability over time is poor. If it exceeds 30% by weight, stickiness may be felt and makeup may be deteriorated.

本発明は用いられる有機変性粘土鉱物は粘土鉱物の結晶
層間に介在する水や交換性カチオンを有機極性化合物や
有機カチオンで置換したものであり、たとえば、ジオク
タデシルジメチルアンモニウム塩変性モンモリロナイ
ト、オクタデシルジメチルベンジルアンモニウム塩変性
モンモリロナイト、ジヘキサデシルメチルアンモニウム
塩変性モンモリロナイトなどが挙げられる。これらの中
から一種または二種以上が任意に選択される。
The organic modified clay mineral used in the present invention is one in which water or an exchangeable cation present between the crystal layers of the clay mineral is replaced with an organic polar compound or an organic cation. For example, dioctadecyldimethylammonium salt modified montmorillonite, octadecyldimethylbenzyl. Examples thereof include ammonium salt-modified montmorillonite and dihexadecylmethyl ammonium salt-modified montmorillonite. One kind or two or more kinds are arbitrarily selected from these.

配合量は本発明のゲル組成物全量中の 0.1〜15重量%の
範囲で選択されるが、好ましくは 0.2〜10重量%であ
る。 0.1重量%未満では増粘効果が十分でなく経時安定
性も悪い。15重量%を越えるとのびが重くなり使用性が
悪くなる。
The blending amount is selected in the range of 0.1 to 15% by weight in the total amount of the gel composition of the present invention, but preferably 0.2 to 10% by weight. If it is less than 0.1% by weight, the thickening effect is insufficient and the stability over time is poor. If it exceeds 15% by weight, spreadability becomes heavy and usability deteriorates.

本発明における水の配合量はゲル組成物全量中の 0.2〜
80重量%の範囲で選択されるが、好ましくは 0.5〜60重
量%である。 0.2重量%未満では増粘効果が十分でなく
経時安定性も悪い。80重量%を越えるとのびが重くなり
好ましくない。
The amount of water in the present invention is 0.2 to the total amount of the gel composition.
It is selected in the range of 80% by weight, preferably 0.5-60% by weight. If it is less than 0.2% by weight, the thickening effect is insufficient and the stability over time is poor. If it exceeds 80% by weight, the spread becomes heavy, which is not preferable.

本発明のフロン増粘組成物を応用した化粧料は上記の必
須成分に加えて、必要に応じてワックス、油脂、保湿
剤、顔料、粉末、樹脂、香料、防腐剤等が配合される。
In addition to the above-mentioned essential components, the cosmetics to which the flon thickening composition of the present invention is applied may further contain waxes, oils and fats, humectants, pigments, powders, resins, fragrances, preservatives and the like, if necessary.

なお、さらにエタノール、イソプロピルアルコール等の
低級アルコールやプロピレングリコール、ジプロピレン
グリコール、1,3-ブチレングリコール等のグリコール類
を組成物全量に対して 0.1〜10重量%加えるとさらに増
粘し安定性を向上させることができる。
In addition, adding 0.1 to 10% by weight of lower alcohols such as ethanol and isopropyl alcohol and glycols such as propylene glycol, dipropylene glycol and 1,3-butylene glycol to the total amount of the composition further increases the viscosity and stability. Can be improved.

〔発明の効果〕〔The invention's effect〕

本発明のフロンを含むゲル組成物は経時安定性が良好で
且つ使用に際してはのびがよくてべたつきがない良好な
使用感触を有し、揮発が速くて清涼感を有する優れたゲ
ル組成物である。
The gel composition containing the chlorofluorocarbon of the present invention is an excellent gel composition having good stability over time, good spreadability and no stickiness in use, and good volatility and refreshing feeling. .

また、粘度すなわち流動性を自由にコントロールできる
ため、化粧料をはじめ、医薬品の基剤や自動車ワック
ス、家具ワックスなど広い範囲にわたって使用すること
ができる。
Further, since the viscosity, that is, the fluidity can be freely controlled, it can be used in a wide range such as cosmetics, pharmaceutical bases, automobile waxes, furniture waxes.

〔実施例〕〔Example〕

次に実施例によって本発明をさらに詳細に説明する。本
発明はこれによい限定されるものではない。配合量は重
量%である。
Next, the present invention will be described in more detail with reference to examples. The present invention is not limited thereto. The blending amount is% by weight.

なお、実施例および比較例の諸特性についての試験法は
次の通り行ったものである。
The test methods for the characteristics of the examples and comparative examples are as follows.

(1)安定性 サンプル管に試料を取り各温度条件に放置し、分離度で
評価(1カ月後判定)。
(1) Stability A sample was taken in a sample tube, left under each temperature condition, and evaluated by the degree of separation (judgment after 1 month).

評価基準 ○:分離なし △:1/5程度分離 ×:2/3以上分離 (2)粘度 ブルックフィールド型粘度計にて測定(30℃)。Evaluation criteria ○: No separation Δ: About 1/5 separation ×: 2/3 or more separation (2) Viscosity Measured with a Brookfield viscometer (30 ° C).

(3)べたつき及びのび 実使用試験による官能評価(パネル20名)。(3) Stickiness and spread Sensory evaluation by actual use test (20 panelists).

評価基準 ○:べたつきなし、のびが軽い。Evaluation criteria ○: No stickiness and light spread.

△:ややべたつく、のびが普通。△: Slightly sticky and spread normally.

×:べたつく、のびが重い。X: Sticky and heavy spread.

〔製法〕 〜をホモディスパーにて撹拌し、筋肉疲労回復剤を
得た。
[Manufacturing Method] was stirred with a homodisper to obtain a muscle fatigue recovery agent.

表中に示した特性から、実施例1、2、3は経時安定性
及び使用性に優れていることが判る。
From the characteristics shown in the table, it is understood that Examples 1, 2, and 3 are excellent in stability over time and usability.

〔製法〕 〜をホモディスパーにて撹拌し、夏用クリームを得
た。
[Production method] was stirred with a homodisper to obtain a summer cream.

表中に示した特性から実施例4、5、6、7、8、9は
経時安定性及び使用性に優れていることが判る。
It can be seen from the characteristics shown in the table that Examples 4, 5, 6, 7, 8, 9 are excellent in stability over time and usability.

※顔料組成 二酸化チタン 40% タルク 25 マイカ 25 黄酸化鉄 2.7 赤酸化鉄 6.5 黒酸化鉄 0.8 〔製法〕 〜をホモディスパーにて撹拌し、耐水性ファンデー
ションを得た。
* Pigment composition Titanium dioxide 40% Talc 25 Mica 25 Yellow iron oxide 2.7 Red iron oxide 6.5 Black iron oxide 0.8 [Production method] ~ was stirred with a homodisper to obtain a water resistant foundation.

表中に示した特性から実施例10、11、12は経時安定性及
び使用性に優れていることが判る。
From the characteristics shown in the table, it is understood that Examples 10, 11 and 12 are excellent in stability over time and usability.

〔製法〕 〜をホモディスパーにて撹拌し、耐水性アイランナ
ーを得た。
[Manufacturing method] was stirred with a homodisper to obtain a water resistant eye runner.

表中に示した特性から実施例13、14、15、16は経時安定
性及び使用性に優れていることが判る。
From the characteristics shown in the table, it is understood that Examples 13, 14, 15, 16 are excellent in stability over time and usability.

〔製法〕 〜をホモディスパーにて撹拌し、つや出しクリーム
を得た。
[Manufacturing Method] was stirred with a homodisper to obtain a polish cream.

実施例17は、家具のつや出しクリームなどにも使用でき
ることを実使用テストにて確認した。
It was confirmed in an actual use test that Example 17 can be used as a polish cream for furniture.

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】常温で液状のフロン1〜90重量%、一般
式(I)、(II)または(III)で示されるポリオキシ
アルキレン変性オルガノポリシロキサンの一種又は二種
以上0.1〜30重量%、有機変性粘土鉱物0.1〜1
5重量%ならびに水0.2〜80重量%を配合すること
を特徴とするフロンを含むゲル組成物。 {一般式(I)、(II)、(III)中、Rはメチル基ま
たは一部がフェニル基、R′は水素または炭素数1〜1
2のアルキル基、pは1〜5の数、qは2〜3の数、
x,m,nは平均数でポリオキシアルキレン変性オルガ
ノポリシロキサンが分子中にポリオキシアルキレン基を
4〜40重量%含有し且つ該ポリオキシアルキレン変性
オルガノポリシロキサンの粘度が25℃において5〜30
00センチストークスになるような数値を表す。}
1. A fluorocarbon liquid 1 to 90% by weight at room temperature, one or more polyoxyalkylene-modified organopolysiloxanes represented by the general formula (I), (II) or (III) 0.1 to 30. % By weight, organically modified clay mineral 0.1-1
A gel composition containing CFCs, characterized in that 5% by weight and 0.2 to 80% by weight of water are blended. {In the general formulas (I), (II) and (III), R is a methyl group or a part thereof is a phenyl group, R'is hydrogen or a carbon number of 1 to 1
2 alkyl groups, p is a number from 1 to 5, q is a number from 2 to 3,
x, m, and n are average numbers, and the polyoxyalkylene-modified organopolysiloxane contains 4 to 40% by weight of polyoxyalkylene groups in the molecule, and the viscosity of the polyoxyalkylene-modified organopolysiloxane is 5 to 30 at 25 ° C.
Represents a value that will be 00 centistokes. }
JP6017885A 1985-03-25 1985-03-25 Gel composition containing CFC Expired - Lifetime JPH0623374B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP6017885A JPH0623374B2 (en) 1985-03-25 1985-03-25 Gel composition containing CFC

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP6017885A JPH0623374B2 (en) 1985-03-25 1985-03-25 Gel composition containing CFC

Publications (2)

Publication Number Publication Date
JPS61218677A JPS61218677A (en) 1986-09-29
JPH0623374B2 true JPH0623374B2 (en) 1994-03-30

Family

ID=13134638

Family Applications (1)

Application Number Title Priority Date Filing Date
JP6017885A Expired - Lifetime JPH0623374B2 (en) 1985-03-25 1985-03-25 Gel composition containing CFC

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Publication number Priority date Publication date Assignee Title
JPS62175416A (en) * 1986-01-28 1987-08-01 Shiseido Co Ltd Cosmetic
JP7389979B2 (en) * 2018-08-22 2023-12-01 株式会社マツモト交商 Gel composition and cosmetics containing the same

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JPS61218677A (en) 1986-09-29

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