JPS61158914A - Hair cosmetic - Google Patents

Hair cosmetic

Info

Publication number
JPS61158914A
JPS61158914A JP27916284A JP27916284A JPS61158914A JP S61158914 A JPS61158914 A JP S61158914A JP 27916284 A JP27916284 A JP 27916284A JP 27916284 A JP27916284 A JP 27916284A JP S61158914 A JPS61158914 A JP S61158914A
Authority
JP
Japan
Prior art keywords
hair
silicone resin
organic silicone
component
amount
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
JP27916284A
Other languages
Japanese (ja)
Other versions
JPH037641B2 (en
Inventor
Hiroaki Yasuhara
安原 宏昭
Yutaka Okunuki
裕 奥貫
Tomiyuki Nanba
富幸 難波
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 JP27916284A priority Critical patent/JPS61158914A/en
Publication of JPS61158914A publication Critical patent/JPS61158914A/en
Publication of JPH037641B2 publication Critical patent/JPH037641B2/ja
Granted 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
    • A61K8/72Cosmetics 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
    • 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
    • A61K8/31Hydrocarbons
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q5/00Preparations for care of the hair
    • A61Q5/12Preparations containing hair conditioners

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 provide a hair cosmetic such as set lotion, hair spray, etc. containing a specific organic silicone resin and a volatile hydrocarbon oil, giving excellent gloss and smooth feeling to the hair, and having high set-keeping property. CONSTITUTION:The objective hair cosmetic contains (A) 0.1-50wt% organic silicone resin of formula (R is 1-6C hydrocarbon group or phenyl; n is 1.0-1.8) and (B) 0.1-99wt% volatile hydrocarbon oil having a boiling point of 60-260 deg.C. When the amount of the component B is high, the cosmetic has the form of a solution, and turns gradually to a solid state by increasing the amount of the component A. An emulsified composition can be produced by compounding the composition further with an aqueous component and a proper surfactant to an extent to keep the water-repellency. It may be compounded further with liquid paraffin, squalane, higher alcohol, medicinal drug component, perfumery, etc.

Description

【発明の詳細な説明】 [産業上の利用分野] 本発明は毛髪に対し、優れた光沢を与え、なめらかな感
触を付与しながら、かつ良好なセット保持力を有する毛
髪化粧料に関する。
DETAILED DESCRIPTION OF THE INVENTION [Industrial Field of Application] The present invention relates to a hair cosmetic that imparts excellent gloss and smooth feel to hair, and has good set-holding power.

[従来の技術] 従来、毛髪をセットし、これを保つ目的では、セットロ
ーション、ヘアスプレィなどが用いられてきた。
[Prior Art] Conventionally, setting lotions, hair sprays, and the like have been used to set and maintain hair.

これら毛髪化粧料には、毛髪固定用の高分子化合物が配
合されている。たとえば、ポリビニルピロリドン系高分
子化合物、酸性ポリビニルエーテル系高分子化合物、酸
性ポリ酢酸ビニル系高分子化合物、酸性アクリル系高分
子化合物、両性アクリル系高分子化合物などである。
These hair cosmetics contain polymer compounds for hair fixation. Examples include polyvinylpyrrolidone polymer compounds, acidic polyvinyl ether polymer compounds, acidic polyvinyl acetate polymer compounds, acidic acrylic polymer compounds, and amphoteric acrylic polymer compounds.

一方、毛髪に光沢やなめらかさを与える目的ではシリコ
ーン油、高級アルコール、流動パラフィン、エステル油
などの油分やカチオン性界面活性剤、カチオン性高分子
化合物、ノニオン性界面活性剤などが配合されている。
On the other hand, for the purpose of giving shine and smoothness to the hair, oils such as silicone oil, higher alcohol, liquid paraffin, and ester oil, as well as cationic surfactants, cationic polymer compounds, and nonionic surfactants are blended. .

しかしながら、上記の毛髪に光沢やなめらかさを与える
目的で配合される油分などは毛髪のセット保持力に対し
ては阻害要因として働いてしまうので、高い七ノド保持
力を有しながら毛髪に優れた光沢やなめらかさを与えら
れる毛髪化粧料はこれまで得られていなかった。
However, the above-mentioned oils added for the purpose of giving shine and smoothness to the hair act as a hindering factor to the hair's set retention power, so it is possible to create a product that has high hair retention power and is excellent for hair. Until now, hair cosmetics that give shine and smoothness have not been available.

[発明が解決しようとする問題点] 本発明者らは、このような事情にかんがみ、優れた七ノ
ド保持力を有しながら、かつ光沢やなめらかさの点でも
満足できる毛髪化粧料を得るべく鋭意研究を行った結果
、特定の有機シリコーン樹脂に加えて揮発性炭化水素油
を用いたならば、上記目的を達成できることを見出し、
この知見にもとづいて本発明を完成するに至った。
[Problems to be Solved by the Invention] In view of the above circumstances, the present inventors sought to obtain a hair cosmetic that has excellent hair retention ability and is also satisfactory in terms of gloss and smoothness. As a result of extensive research, we discovered that the above objectives could be achieved by using a volatile hydrocarbon oil in addition to a specific organic silicone resin.
Based on this knowledge, we have completed the present invention.

c問題点を解決するための手段] すなわち、本発明は、下記(A)で示される有機シリコ
ーン樹脂0.1〜50重量%および下記(B)で示され
る揮発性炭化水素油0.1〜99重量%を含有すること
を特徴とする毛髪化粧料である。
Means for Solving Problems c] That is, the present invention provides 0.1 to 50% by weight of an organic silicone resin shown in (A) below and 0.1 to 50% by weight of a volatile hydrocarbon oil shown in (B) below. This hair cosmetic is characterized by containing 99% by weight.

(A)  平均式 RnSiO(”   (Rは炭素数
1〜6までの炭化水素基またはフェニル基を表し、nは
1.0から 1.8までの値を表す)の単位からなる有
機シリコーン樹脂。
(A) An organic silicone resin comprising units of the average formula RnSiO(" (R represents a hydrocarbon group having 1 to 6 carbon atoms or a phenyl group, and n represents a value from 1.0 to 1.8).

(B)  室温における沸点が60〜260℃の範囲に
ある揮発性炭化水素油。
(B) A volatile hydrocarbon oil having a boiling point in the range of 60 to 260°C at room temperature.

本発明で用いる上記(A)で示される有機シリコーン樹
脂はR35iO工 単位、R25io単位、R5103
単位およびSiO単位のうちの適当な組合せからなり、
その割合は平均式Rn5i04二ニー(nは1.0から
 1.8までの値を表す)を満足するように選ばれ、約
1500〜1ooooまでの平均分子量を有することが
望ましい。
The organic silicone resin represented by (A) used in the present invention includes R35iO unit, R25io unit, R5103
consisting of an appropriate combination of units and SiO units,
The proportions are selected to satisfy the average formula Rn5i04, where n represents a value from 1.0 to 1.8, and preferably have an average molecular weight of about 1500 to 1oooo.

上記有機シリコーン樹脂はベンゼンに可溶であり、各種
の方法で製造し得る。−例をあげると、一般式R3Si
X、 R25iX2 、R51X3およびSiX+  
(Xは加水分解し得る基、たとえば塩素、臭素、弗素、
アルコキシ、たとえばメトキシ、エトキシなどの基、ア
シロキシ基を表す)で示される化合物を、目的とする樹
脂組成に応じてトルエン、ベンゼン、キシレンなどのご
とき適当な溶媒に添加し、次いでこの溶媒を適当な酸性
溶媒中における希望する加水分解および共縮合を得るに
充分な量の水中に加える。こうして得られた二相系から
水相を除去し、残留する樹脂状物質を重炭酸ナトリウム
あるいは他のアルカリ性物質の充分量を用いて中和し、
溶媒を留去すれば目的の有機シリコーン樹脂が得られる
The above organic silicone resin is soluble in benzene and can be produced by various methods. -For example, general formula R3Si
X, R25iX2, R51X3 and SiX+
(X is a hydrolyzable group, such as chlorine, bromine, fluorine,
A compound represented by alkoxy (e.g., methoxy, ethoxy, etc. group, acyloxy group) is added to a suitable solvent such as toluene, benzene, xylene, etc. depending on the desired resin composition, and then this solvent is mixed with a suitable solvent. Add in sufficient amount of water to obtain the desired hydrolysis and co-condensation in an acidic solvent. removing the aqueous phase from the resulting two-phase system and neutralizing the remaining resinous material with a sufficient amount of sodium bicarbonate or other alkaline substance;
By distilling off the solvent, the desired organic silicone resin can be obtained.

本発明における有機シリコーン樹脂の配合量は毛髪化粧
料全量中の0.1〜50重量%である。
The amount of organic silicone resin blended in the present invention is 0.1 to 50% by weight based on the total amount of the hair cosmetic.

また、本発明で用いる揮発性炭化水素油は室温における
沸点が60〜260℃の範囲にある炭化水素油であり、
たとえば、アイソパー(登録商標)A、同C1同D、同
E、同G、同H1同K、同し、同M(エクソン社)、シ
ェルゾール<登録0標) 71、(シェル社)、ツルト
ロール(登M商+り  100、同130、同220(
フィリップ社)などをあげことができる。
Further, the volatile hydrocarbon oil used in the present invention is a hydrocarbon oil having a boiling point in the range of 60 to 260°C at room temperature,
For example, Isopar (registered trademark) A, C1 D, E, G, H1 K, Isopar M (Exxon), Shellzol (registered trademark) 71, (Shell), Tsurtrol. (Registered trading company + 100, 130, 220 (
Philips Co., Ltd.).

これらは、いずれも揮発性であって、かつ有機シリコー
ン樹脂に対して溶媒となり得る。
All of these are volatile and can act as a solvent for the organic silicone resin.

配合量は、毛髪化粧料全量中の0.1〜99重量%であ
る。
The blending amount is 0.1 to 99% by weight based on the total amount of hair cosmetics.

上記の必須成分を含有してなる毛髪化粧料はその配合量
に応じて、溶液状から固型状までを呈する。すなわち、
揮発性炭化水素油が多いときは溶液状を呈し、有機シリ
コーン樹脂が増量するにしたがって固形状になる。
Hair cosmetics containing the above-mentioned essential ingredients take on the form of a solution to a solid depending on the amount of the ingredients. That is,
When the amount of volatile hydrocarbon oil is large, it takes the form of a solution, and as the amount of organic silicone resin increases, it becomes solid.

当然のことながら、上記必須成分に加えて、水性成分お
よび適切な界面活性剤を配合して乳化技術を駆使するこ
とによって、撥水性をうしなわない範囲で油中水型ある
いは水中油型の乳化組成物にすることも可能である。
Naturally, in addition to the above essential ingredients, by blending aqueous components and appropriate surfactants and making full use of emulsification technology, water-in-oil or oil-in-water emulsion compositions can be created without sacrificing water repellency. It is also possible to turn it into an object.

本発明の毛髪化粧料には上記の必須構成成分に加えて、
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、さらに流動パラフィン、スクワラン、ラノリン誘
導体、高級アルコール、各種エステル油、シリコーン油
、ポリアルキレングリコールポリエーテルおよびそのカ
ルボン酸オリゴエステル化合物、テルペン系炭化水素油
などの油分、カチオン性界面活性剤、カチオン性高分子
化合物、ノニオン性界面活性剤、薬剤、香料を配合して
も良い。これら他の成分を適量配合しても本発明の毛髪
化粧料は毛髪のセット保持力を阻害されることは少ない
In addition to the above-mentioned essential components, the hair cosmetic of the present invention includes:
Depending on the purpose, liquid paraffin, squalane, lanolin derivatives, higher alcohols, various ester oils, silicone oils, polyalkylene glycol polyethers and carboxylic acid oligoesters thereof, within a quantitative and qualitative range that does not impair the effects of the present invention. Compounds, oils such as terpene hydrocarbon oils, cationic surfactants, cationic polymer compounds, nonionic surfactants, drugs, and fragrances may be blended. Even if appropriate amounts of these other ingredients are blended, the hair cosmetic composition of the present invention is unlikely to impede the hair set retention ability.

以下、実施例により本発明をさ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
量は全て重量%である。
Hereinafter, the present invention will be explained in more detail with reference to Examples. The present invention is not limited by these. All compounding amounts are weight %.

実施例1 ヘアスプレィ ■アイソパー(登録商標)C (沸点98〜1)3°c)        65.5■
アイソパー(登録商標)H (沸点171〜193℃)       15.0■約
8000の分子量を有し、かつ (C6H5)SiO−r 単位: (C1(3) 2 SiO単位= 5.67 : ]  からなる平均式 %式% で表される有機シリコーン樹脂    18.0■メチ
ルフエニルポリシロキサン     1.0■P、0.
E、 (4モル)ステアリルエーテル 0.5■香料 
              通量■〜■を70〜80
°Cで攪拌熔解し、■を加えて原液とする。原液30重
量部に対して噴射ガス(フロン(登録商標)1):同1
2=40: 60) 70重量部を加えてエアゾール罐
中に充填してヘアスプレィを得た。
Example 1 Hairspray Isopar (registered trademark) C (boiling point 98-1) 3°C) 65.5
Isopar (registered trademark) H (boiling point 171-193°C) has a molecular weight of 15.0 ■ about 8000 and consists of (C6H5)SiO-r units: (C1(3) 2 SiO units = 5.67: ) Organic silicone resin expressed by average formula % formula % 18.0■Methylphenylpolysiloxane 1.0■P, 0.
E, (4 mol) stearyl ether 0.5 ■Fragrance
Passage ■~■70~80
Stir and melt at °C, and add ① to make a stock solution. Injection gas (Freon (registered trademark) 1) per 30 parts by weight of stock solution: 1
2=40:60) 70 parts by weight was added and filled into an aerosol can to obtain a hair spray.

実施例2 セットローション ■ツルトロール(登録商標) 100 (沸点160〜175℃)      10.0■約3
000の分子量を有し、かつ (CH3) 3 SiO上 単位: λ Si02単位= o、s: 1からなる平均式(CI+
3 ) +、33 SiO+、3+で表される有機シリ
コーン樹脂     7.0■セチル−2−エチルヘキ
サノエート1.0■塩化ステアリルトリメチルアンモニ
ウム0.2■エチルアルコール          7
0.0■精製水               残余■
香料                通量■〜■を7
0〜80℃で攪拌熔解し、別に■〜■を溶解したものを
加え、さらに■を加えてセットローションを得た。
Example 2 Set lotion ■ Tsurutrol (registered trademark) 100 (boiling point 160-175°C) 10.0 ■ Approx. 3
000 and has an average formula (CI+
3) +, 33 SiO+, organic silicone resin represented by 3+ 7.0 ■ Cetyl-2-ethylhexanoate 1.0 ■ Stearyltrimethylammonium chloride 0.2 ■ Ethyl alcohol 7
0.0■Purified water remainder■
Fragrance amount ■~■ 7
The mixture was stirred and melted at 0 to 80° C., separately dissolved ① to ③ were added, and ③ was further added to obtain a setting lotion.

比較例1 ヘアスプレィ ■メチルビニルエーテルとマレイン酸 ハーフエチルエステルとの−1”重合物1B、0■アミ
ノメチルプロパツール      0.8■メチルフエ
ニルポリシロキサン     1.0φP、O,E、 
(4モル)ステアリルエーテル 0.5■エチルアルコ
ール          83.5■香料      
         適量■〜■を攪拌溶解して原液とす
る。原液30重量部に対して噴射ガス(フロン(登録商
標)1):同12=40: 60) 70重量部を加え
てエアゾール罐中に充填してヘアスプレィを得た。
Comparative Example 1 Hairspray ■-1" polymer of methyl vinyl ether and maleic acid half ethyl ester 1B, 0 ■ Aminomethyl propatool 0.8 ■ Methyl phenyl polysiloxane 1.0φP, O, E,
(4 moles) Stearyl ether 0.5■Ethyl alcohol 83.5■Fragrance
Stir and dissolve appropriate amounts of ■ to ■ to obtain a stock solution. To 30 parts by weight of the stock solution, 70 parts by weight of a propellant gas (Freon (registered trademark) 1: 12 = 40: 60) was added and filled into an aerosol can to obtain a hair spray.

比較例2 セットローション ■ビニルピロリドンと酢酸ビニルとの 共重合物       7.0 ■セチルー2−エチルヘキサノエート1.0■lfi化
ステアリルトリメチルアンモニウム0.2■エチルアル
コール          70.0■精製水    
           残余■香料         
       通量■■を攪拌溶解し、さらに■〜■お
よび■を熔解してセンドローションを得た。
Comparative Example 2 Set lotion ■ Copolymer of vinyl pyrrolidone and vinyl acetate 7.0 ■ Cetyl-2-ethylhexanoate 1.0 ■ lfi-formed stearyltrimethylammonium 0.2 ■ Ethyl alcohol 70.0 ■ Purified water
Residue ■Fragrance
The total amount ■■ was stirred and dissolved, and then ■~■ and ■ were further melted to obtain a send lotion.

実施例1.2および比較例1.2について以下の実験を
行い、性能を評価した。
The following experiment was conducted for Example 1.2 and Comparative Example 1.2, and the performance was evaluated.

市販毛髪ストランド(重さ3g、幅2cm、長さ20c
m)に実施例1または比較例1を5秒間噴霧する。別に
、同種の毛髪ストランドに実施例2または比較例2を0
.5g塗布する。これら試料をカールし、充分に乾燥さ
せた後、実験に供した。
Commercially available hair strands (weight 3g, width 2cm, length 20c)
Example 1 or Comparative Example 1 is sprayed onto m) for 5 seconds. Separately, apply Example 2 or Comparative Example 2 to hair strands of the same type.
.. Apply 5g. These samples were curled, thoroughly dried, and then used for experiments.

すなわち、4種のカールした毛髪ストランドを30℃9
0%の恒温恒湿下で24時間放置する。元の毛髪ストラ
ンドの長さくL)、最初のカールの径(Lo)、24時
間放置後のカールの径(Lt)を測定し、次式にもとづ
いて算出したカールリテンションをもってセット力とし
た。数値が大きいほどセット力が強いことを表す。
That is, four types of curled hair strands were heated at 30°C9.
Leave it for 24 hours under constant temperature and humidity of 0%. The length of the original hair strand (L), the diameter of the initial curl (Lo), and the diameter of the curl after being left for 24 hours (Lt) were measured, and the curl retention calculated based on the following formula was defined as the setting force. The larger the number, the stronger the setting force is.

(以下余白) また、光沢、なめらかさについてはそれぞれ官能で評価
した。
(Hereinafter referred to as blank space) In addition, gloss and smoothness were each evaluated by sensory evaluation.

○・・・・・優れている △・・・・・普通 ×・・・・・劣っている 結果を表1に示す。○・・・Excellent △・・・・・・Normal ×・・・Inferior The results are shown in Table 1.

表1 従来のヘアスプレィ、セットローションに比べて、本発
明の毛髪化粧料が光沢、なめらかさ、セノトカで優れて
いることが明らかである。
Table 1 It is clear that the hair cosmetics of the present invention are superior in gloss, smoothness, and texture compared to conventional hair sprays and setting lotions.

(以下余白) 実施例3 ポマード ■マイクロクリスタリンワックス     780■ス
クワラン             13.0■シエル
ゾール(登録商標)71 (沸点173〜195℃)     13.0■アイソ
パー(登録商標)E (沸点1)6〜143℃)     12.0■約50
00の分子量を有し、かつ (CH3) 3 SiOと 単位: 5iO2単位= 1.5: 1からなる平均式(CH3
)+y8 Sin、。
(Leaving space below) Example 3 Pomade Microcrystalline wax 780 Squalane 13.0 Sielzol (registered trademark) 71 (boiling point 173-195°C) 13.0 ■ Isopar (registered trademark) E (boiling point 1) 6-143°C ) 12.0 ■ Approx. 50
It has a molecular weight of 00, and has an average formula (CH3) 3 SiO and 5iO2 units = 1.5: 1.
)+y8 Sin,.

で表される有機シリコーン樹脂    45.0■P、
0.E、 (10モル)硬化ヒマシ油トリイソステアレ
ート10.0 ■香料                 ′a量〜■
〜■を7θ〜80℃で攪拌溶解し、■を加えて冷却し、
ポマードを得た。
Organic silicone resin represented by 45.0■P,
0. E, (10 mol) hydrogenated castor oil triisostearate 10.0 ■Fragrance 'a amount~■
~■ is stirred and dissolved at 7θ~80°C, and ■ is added and cooled.
Got pomade.

実施例3は従来のポマードに比較して、特異な匂いも少
なく、さっばりとのびのよい使用感で、かつ光沢、なめ
らかさおよびセット保持力にも優れたポマードであった
Compared to conventional pomades, Example 3 had less peculiar odor, felt light and spreadable, and had excellent gloss, smoothness, and set retention power.

実施例4 ヘアリキッド ■アイソパー(登録商標)A (沸点66〜70℃)        30.0■ツル
トロール(登録商標)A (沸点240〜260℃)     35.0■約20
00の分子量を有し、かつ (C1)3) 3 SiO上 単位: (C6H5) 2 SiO単位: (Cs Hs ) SiO上 単位: Si02単位= o、9:  o、t:  o、2: 
1からなる平均式 %式% で表される有機シリコーン樹脂    30.0■セチ
ル−2−エチルヘキサノエート5.0■香料     
            適量■〜■を50〜60℃で
攪拌溶解し、■を加えてヘアリキッドを得た。
Example 4 Hair liquid ■ Isopar (registered trademark) A (boiling point 66-70°C) 30.0 ■ Tsurutrol (registered trademark) A (boiling point 240-260°C) 35.0 ■ Approx. 20
00, and (C1)3) 3 units on SiO: (C6H5) 2 SiO units: (Cs Hs ) units on SiO: Si02 units = o, 9: o, t: o, 2:
Organic silicone resin represented by the average formula % formula % consisting of 1 30.0 ■ Cetyl-2-ethylhexanoate 5.0 ■ Fragrance
Appropriate amounts of ■ to ■ were stirred and dissolved at 50 to 60°C, and ■ was added to obtain a hair liquid.

実施例4は従来のへアリキッドに比較して、さっばりと
した使用感で、かつ光沢、なめらかさおよびセット保持
力にも優れたヘアリキッドであった。
Example 4 was a hair liquid that had a lighter feel and was superior in gloss, smoothness, and set holding power compared to conventional hair liquids.

実施例5 ヘアクリーム ■ツルトロール(登録商標)130 (沸点170〜208℃)      10.0■約5
000の分子量ををし、かつ (CH3) 3 SiO上 単位: 5iO2単位−0.5:1からなる 平均式(CH3)1.。5iO1,5 で表される有機シリコーン樹脂    3.0■流動パ
ラフイン           7.0■脱臭ラノリン
             4.0■セチルアルコール
          2.0■ソルビタンモノステアレ
ート      2.5■P、0.E、 (50モル)
硬化ヒマシ油    2.0■プロピレングリコール 
       5.0■防腐剤           
    通量0精製水               
残余■〜■を70〜80℃で攪拌溶解し、■〜[相]を
溶解したものの中に加えて乳化し、ヘアクリームを得た
Example 5 Hair cream ■ Tsurutrol (registered trademark) 130 (boiling point 170-208°C) 10.0 ■ Approx. 5
000, and the average formula (CH3)1. . Organic silicone resin expressed by 5iO1,5 3.0■Liquid paraffin 7.0■Deodorized lanolin 4.0■Cetyl alcohol 2.0■Sorbitan monostearate 2.5■P, 0. E, (50 moles)
Hydrogenated castor oil 2.0 ■ Propylene glycol
5.0 ■ Preservative
0 volume purified water
Residues (1) to (2) were stirred and dissolved at 70 to 80°C, and added to the dissolved phase (1) to (phase) to emulsify to obtain a hair cream.

実施例5は従来のヘアクリームに比較して、さっばりと
のびがよく、かつ光沢、なめらかさおよびセント保持力
にも優れたヘアリキッドであった。
Example 5 was a hair liquid that spread easily and had better gloss, smoothness, and cent retention power than conventional hair creams.

実施例6 ブローローション ■ツルトロール(登録商標) 100 (沸点160〜175°C)      l、Q■約3
000の分子量を有し、かつ (CH3) 3 SiO上 単位: 5iO2単位= o、s: 1からなる平均式(CH3
)1.33 sho、、、+で表される有機シリコーン
樹脂     0.3■プロピレングリコール    
    3.0■塩化ジステアリルジメチルアンモニウ
ム0.3■第4flkm素に有セルロースエーテル  
0.05■エチルアルコール          ?0
.0■香料                通量■精
製水               残余■■を70〜
80”Cで攪拌溶解した後、30’cに冷却する。これ
を■〜■を熔解したものに加えて攪拌混合してブローロ
ーションを得た。
Example 6 Blow lotion ■ Tsurutrol (registered trademark) 100 (boiling point 160-175°C) l, Q ■ Approx. 3
000 and has an average formula (CH3) on SiO unit: 5iO2 unit = o, s: 1
) 1.33 sho, , + organic silicone resin 0.3 ■ Propylene glycol
3.0 ■ Distearyl dimethyl ammonium chloride 0.3 ■ Cellulose ether in the 4th flkm element
0.05 ■Ethyl alcohol? 0
.. 0 ■Fragrance volume ■Purified water Remaining ■■ 70 ~
After stirring and dissolving at 80"C, the mixture was cooled to 30'C. This was added to the melted materials ① to ③ and mixed with stirring to obtain a blow lotion.

実施例6は従来のものに比較して、光沢、なめらかさお
よびセント保持力においてはるかに優れたブローローシ
ョンであった。
Example 6 was a blow lotion that was much better in shine, smoothness, and cent retention than the conventional one.

実施例7 リンス ■塩化スステアリルトリメチルアンモニウム50■ステ
アリルアルコール         3.0■P、O,
E、 (4モル)ステアリルエーテル 1.5■アイソ
パー(登録商標)E (沸点1)6〜143℃)5.0 ■約500Cjの分子量を有し、かつ (CH3) 3 SiO± 単位: 5iO2単位= 0.5: 1からなる平均式(CII
3 )、。5iO1,yで表される有機シリコーン樹脂
     4.0■クエン酸            
     0.1■ジプロピレングリコール     
   3.0■防腐剤               
通量■香料                適量[相
]色剤                適量■精製水
              残余■〜■を70〜80
℃で攪拌溶解する(油相)。■および■〜■を70〜8
0℃で攪拌熔解する(水相)水相と油相を攪拌混合した
後30℃まで冷却してヘアリンスを得た。
Example 7 Rinse ■ stearyltrimethylammonium chloride 50 ■ stearyl alcohol 3.0 ■ P, O,
E, (4 mol) stearyl ether 1.5 ■ Isopar (registered trademark) E (boiling point 1) 6-143°C) 5.0 ■ having a molecular weight of about 500 Cj, and (CH3) 3 SiO± units: 5iO2 units = 0.5: Average formula consisting of 1 (CII
3). Organic silicone resin represented by 5iO1,y 4.0 ■ Citric acid
0.1 ■ Dipropylene glycol
3.0 ■ Preservative
Amount ■Fragrance Appropriate amount [Phase] Coloring agent Appropriate amount ■Purified water Remaining ■~■ 70~80
Stir and dissolve at °C (oil phase). ■and ■~■70~8
A hair rinse was obtained by stirring and mixing the aqueous phase and the oil phase, which were stirred and melted at 0°C, and then cooled to 30°C.

実施例7は従来のものに比較して、毛髪に豊かな光沢を
与え、さらっとした感触で、セットしやすい毛髪に仕上
げる効果を有し、その後のセントのもちもよいリンスで
あった。
Compared to the conventional rinse, Example 7 had the effect of giving hair a rich luster, a silky feel, and a finish that was easy to set, and had a good conditioner after use.

[発明の効果]    ′ 本発明の毛髪化粧料は、毛髪に豊かな光沢となめらかさ
を与え、かつ毛髪に対して優れたセフ)保持力を有する
毛髪化粧料である。
[Effects of the Invention] ' The hair cosmetic of the present invention is a hair cosmetic that gives rich luster and smoothness to hair and has excellent hair-holding power.

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樹脂0.1
〜50重量%および下記(B)で示される揮発性炭化水
素油0.1〜99重量%を含有することを特徴とする毛
髪化粧料。 (A)平均式RnSiO_(_4_−_n_/_2_)
(Rは炭素数1〜6までの炭化水素基またはフェニル基 を表し、nは1.0から1.8までの値を表す)の単位
からなる有機シリコーン樹脂。 (B)室温における沸点が60〜260℃の範囲にある
揮発性炭化水素油。
(1) Organosilicone resin shown below (A) 0.1
50% by weight and 0.1 to 99% by weight of a volatile hydrocarbon oil represented by (B) below. (A) Average formula RnSiO_(_4_-_n_/_2_)
(R represents a hydrocarbon group having from 1 to 6 carbon atoms or a phenyl group, and n represents a value from 1.0 to 1.8). (B) A volatile hydrocarbon oil having a boiling point in the range of 60 to 260°C at room temperature.
JP27916284A 1984-12-29 1984-12-29 Hair cosmetic Granted JPS61158914A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP27916284A JPS61158914A (en) 1984-12-29 1984-12-29 Hair cosmetic

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP27916284A JPS61158914A (en) 1984-12-29 1984-12-29 Hair cosmetic

Publications (2)

Publication Number Publication Date
JPS61158914A true JPS61158914A (en) 1986-07-18
JPH037641B2 JPH037641B2 (en) 1991-02-04

Family

ID=17607310

Family Applications (1)

Application Number Title Priority Date Filing Date
JP27916284A Granted JPS61158914A (en) 1984-12-29 1984-12-29 Hair cosmetic

Country Status (1)

Country Link
JP (1) JPS61158914A (en)

Cited By (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6322010A (en) * 1986-04-04 1988-01-29 ザ、プロクタ−、エンド、ギヤンブル、カンパニ− Hair treatment composition
JPH02188518A (en) * 1989-01-14 1990-07-24 Nippon Petrochem Co Ltd Hairdressing
JPH02255608A (en) * 1989-03-28 1990-10-16 Pola Chem Ind Inc Permanent waving agent
US4983377A (en) * 1989-10-31 1991-01-08 The Procter & Gamble Company Silicone hairspray compositions
US4983383A (en) * 1988-11-21 1991-01-08 The Procter & Gamble Company Hair care compositions
US4983418A (en) * 1989-10-31 1991-01-08 The Procter & Gamble Company Silicone hairspray compositions
US5100657A (en) * 1990-05-01 1992-03-31 The Procter & Gamble Company Clean conditioning compositions for hair
EP0492657A1 (en) 1990-12-28 1992-07-01 Nippon Unicar Company Limited Cosmetic formulations
JPH05139932A (en) * 1991-11-12 1993-06-08 Kao Corp Hair cosmetic
JPH09165317A (en) * 1995-10-12 1997-06-24 Shiseido Co Ltd Oil-in-water type emulsifying 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
JP2011132246A (en) * 2009-12-23 2011-07-07 L'oreal Sa Cosmetic composition containing at least one volatile linear alkane and at least one cationic surfactant in specific ratio of volatile linear alkane/cationic surfactant

Cited By (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0729906B2 (en) * 1986-04-04 1995-04-05 ザ、プロクタ−、エンド、ギヤンブル、カンパニ− Hairdressing composition
JPS6322010A (en) * 1986-04-04 1988-01-29 ザ、プロクタ−、エンド、ギヤンブル、カンパニ− Hair treatment composition
US4983383A (en) * 1988-11-21 1991-01-08 The Procter & Gamble Company Hair care compositions
JPH02188518A (en) * 1989-01-14 1990-07-24 Nippon Petrochem Co Ltd Hairdressing
JPH02255608A (en) * 1989-03-28 1990-10-16 Pola Chem Ind Inc Permanent waving agent
US4983377A (en) * 1989-10-31 1991-01-08 The Procter & Gamble Company Silicone hairspray compositions
US4983418A (en) * 1989-10-31 1991-01-08 The Procter & Gamble Company Silicone hairspray compositions
US5100657A (en) * 1990-05-01 1992-03-31 The Procter & Gamble Company Clean conditioning compositions for hair
EP0492657A1 (en) 1990-12-28 1992-07-01 Nippon Unicar Company Limited Cosmetic formulations
JPH05139932A (en) * 1991-11-12 1993-06-08 Kao Corp Hair cosmetic
US5676938A (en) * 1992-09-29 1997-10-14 Toshiba Silicone Co., Ltd. Cosmetic composition
JPH09165317A (en) * 1995-10-12 1997-06-24 Shiseido Co Ltd Oil-in-water type emulsifying composition
US6991782B2 (en) 2000-06-19 2006-01-31 L'oréal Cosmetic compositions comprising at least one polymethylsilsesquioxane film former
JP2011132246A (en) * 2009-12-23 2011-07-07 L'oreal Sa Cosmetic composition containing at least one volatile linear alkane and at least one cationic surfactant in specific ratio of volatile linear alkane/cationic surfactant

Also Published As

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JPH037641B2 (en) 1991-02-04

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