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JPH04359912A - New copolymer and cosmetic containing same - Google Patents

New copolymer and cosmetic containing same

Info

Publication number
JPH04359912A
JPH04359912A JP13478391A JP13478391A JPH04359912A JP H04359912 A JPH04359912 A JP H04359912A JP 13478391 A JP13478391 A JP 13478391A JP 13478391 A JP13478391 A JP 13478391A JP H04359912 A JPH04359912 A JP H04359912A
Authority
JP
Japan
Prior art keywords
meth
silicone
acrylic acid
hair
copolymer
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.)
Pending
Application number
JP13478391A
Other languages
Japanese (ja)
Inventor
Yoshiaki Ito
嘉昭 伊藤
Hiroaki Iwasaki
岩▲崎▼ 裕明
Katsumi Mita
三田 勝巳
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.)
Kao Corp
Original Assignee
Kao Corp
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 Kao Corp filed Critical Kao Corp
Priority to JP13478391A priority Critical patent/JPH04359912A/en
Publication of JPH04359912A publication Critical patent/JPH04359912A/en
Pending legal-status Critical Current

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  • Cosmetics (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Macromonomer-Based Addition Polymer (AREA)

Abstract

PURPOSE:To obtain a silicone/(meth)acrylic acid copolymer excellent in film- forming properties and lubricity, etc., by polymerizing (meth)acrylic acid with a specified silicone macromer in the presence of a radical polymerization initiator. CONSTITUTION:(Meth)acrylic acid or its salt of formula I (wherein R<1> is H or methyl) and a silicone macromer of formula II (wherein X is a radical- polymerizable group; R<2>, R<3>, R<4>, R<5> and R<6> are each methyl, alkoxy, (un) substituted phenol or phenoxyl; m is 1-10; and n is 5-150) are polymerized in the presence of a radical polymerization initiator (e.g. 2,2'-azobis-isobutyronitrile) to produce a silicone/(meth)acrylic acid copolymer. This copolymer has a property of forming a thin silicone film on the surface of a coating film, can give a good touch when applied, and is lowly sticky when applied as a hair care preparation.

Description

【発明の詳細な説明】 【0001】 【産業上の利用分野】本発明は優れた被膜形成性、潤滑
性、増粘性等を有する新規なシリコーン/(メタ)アク
リル酸共重合体及びこれを含有する化粧料に関する。 【0002】 【従来の技術】化粧料に望まれる要求は高くなり、一般
に化粧膜に良好な特性を付与するため、種々の被膜形成
剤が用いられるようになっている。特にヘアスプレー、
セットローション等の毛髪化粧料においては、整髪力、
セット保持力等を付与する目的で、被膜形成樹脂が配合
されている。従来、この被膜形成樹脂としては、ポリビ
ニルピロリドン、ポリビニルピロリドン/酢酸ビニル共
重合体、酢酸ビニル/クロトン酸共重合体などが用いら
れている。さらに、特開平2−25411号には、被膜
形成剤として、シリコーン化合物とアクリレートを主体
とする共重合体を用いた化粧料が記載され、耐湿性の被
膜を形成することが開示されている。また、種々の皮膚
及び毛髪化粧料には、剤型により増粘剤が配合されてお
り、当該増粘剤として種々の水溶性高分子物質が使用さ
れている。 【0003】 【発明が解決しようとする課題】しかしながら、従来毛
髪化粧料に配合されている被膜形成樹脂は、通常使用す
る場合にはある程度のセット保持力を有しているものの
、高湿度下においては、吸湿により粘着性を増し、更に
流動性となり、毛髪のセットを充分に維持できなかった
。特開平2−25411号の共重合体も高湿度のセット
性は改良されているものの、溶媒としてイソパラフィン
等の炭化水素、揮発性シリコーン等を必要とし、水溶性
が悪いものであった。毛髪化粧料はシャンプー洗浄で容
易に除去できなければならず、一方では水溶性が、他方
では低い吸湿性が要求されている。この相反する要求を
同時に満たすことは困難であり、従来、前述の如くやむ
を得ず水溶性を断念して、他の溶剤又は溶剤混合物を用
いる場合が多かった。 【0004】また、ヘアスプレー等のセット剤は、乾燥
後の髪がゴワついたり、ガサついたりするのを抑えるた
め、多量の油剤や活性剤を含有している。この油剤や活
性剤の配合は、被膜形成樹脂の毛髪親和性を低下させ、
毛髪のセット保持力を低下させ、また毛髪に塗布後の油
剤、活性剤の手うつりによるベタつき等を生じるなどの
問題となっていた。さらにブラッシング等により毛髪表
面の樹脂被膜が剥離する、いわゆるフレーキングが生じ
、髪のつやが悪くなる等の問題もあった。なお、このフ
レーキングは増粘剤として配合した水溶性高分子物質に
よっても生じることが多かった。 【0005】従って、被膜形成性だけでなく、潤滑性、
増粘性等を有する新規なポリマー、及びこれを配合し、
塗布した時の感触が良好で、特に毛髪に塗布した時、高
湿度下においても優れた整髪力、セット保持力を有する
化粧料が望まれていた。 【0006】 【課題を解決するための手段】かかる実情において、本
発明者らは鋭意研究を行なった結果、(メタ)アクリル
酸又はその塩とシリコーンマクロマーを重合させて得ら
れるシリコーン/(メタ)アクリル酸共重合体が優れた
被膜形成能、潤滑性、増粘性等の性質を有し、更にこれ
を配合した化粧料は、塗布時の感触が非常に良好で、し
かも高湿度下においてもベタつきが少なく、吸湿性を抑
制し、優れた整髪力、セット保持力を有することを見出
し、本発明を完成した。 【0007】すなわち、本発明は、(a)及び(b)(
a)式(1) 【0008】 【化3】 【0009】〔式中、R1は水素原子又はメチル基を示
す〕で表わされる(メタ)アクリル酸又はその塩(b)
式(2) 【0010】 【化4】 【0011】〔式中、Xはラジカル重合性基を示し、R
2、R3、R4、R5及びR6は同一又は異なってもよ
く、メチル基、アルコキシル基、置換されていてもよい
フェニル基又は置換されていてもよいフェノキシル基を
示し、mは1〜10の整数を示し、nは5〜150の整
数を示す〕で表わされるシリコーンマクロマーをラジカ
ル重合開始剤の存在下に重合させて得られるシリコーン
/(メタ)アクリル酸共重合体並びに当該共重合体を含
有する化粧料を提供するものである。 【0012】本発明共重合体の製造に用いられる(a)
成分の(メタ)アクリル酸の塩としては、ナトリウム塩
、カリウム塩等のアルカリ金属塩に代表される無機塩、
第4級アンモニウム塩に代表される有機塩等が挙げられ
る。これら(a)成分は単独又は2種以上を組合わせて
用いることができ、モノマー全体の10〜95重量%(
以下、単に「%」で示す)、特に40〜80%用いるの
が好ましい。 【0013】(b)成分のシリコーンマロクマーは前記
式(2)で表わされ、式中、Xで示されるラジカル重合
性基としては、ビニル基、(メタ)アクリロイル基、ビ
ニルベンジル基、スチリル基、(メタ)アクリルアミド
基、ビニルエーテル基、ビニルエステル基などが挙げら
れる。これらシリコーンマクロマーの具体例としては、
ポリジメチルシロキシプロピル(メタ)アクリル酸エス
テル、ポリジメチルシロキシプロピルビニルベンジルエ
ーテル、ポリメチルフェニルシロキシペンテン、ポリジ
メチルシロキシプロピル(メタ)アクリルアミド、ポリ
ジメチルシロキシプロピル酸ビニルベンジレート、ポリ
メチルフェニルシロキシエトキシエチレン等が挙げられ
、これらのうち特にポリジメチルシロキシプロピル(メ
タ)アクリル酸エステル、ポリジメチルシロキシプロピ
ル(メタ)アクリルアミド等が好ましい。これら(b)
成分は単独又は2種以上を組合わせて用いることができ
、モノマー全体の5〜90%、特に20〜60%用いる
のが好ましい。 【0014】本発明のシリコーン/(メタ)アクリル酸
共重合体は、上記(a)成分及び(b)成分を組合わせ
、ラジカル重合開始剤の存在下、バルク重合法、溶液重
合法、懸濁重合法、乳化重合法等の公知の重合法により
重合させることにより製造される。この時、上記2種の
モノマー以外のモノマーを本発明の効果を損なわない範
囲で共に重合させることも出来る。これらのうち、特に
溶液重合法により製造するのが有利である。溶液重合法
で用いる溶媒としては極性有機溶剤が好ましく、水混和
性有機溶剤を水と混合して用いることもできる。かかる
有機溶剤としては、例えばメタノール、エタノール、プ
ロパノール等の炭素数1〜3の脂肪族アルコール;アセ
トン、メチルエチルケトン等のケトンなどが挙げられ、
これらのうち特にメタノール、エタノール、アセトン又
はこれらと水との混合液が好ましい。これら有機溶剤は
単独又は2種以上を組合わせて用いることができる。 【0015】ラジカル重合開始剤としては、例えば2,
2′−アゾビスイソブチロニトリル、2,2′−アゾビ
ス(2,4−ジメチルバレロニトリル)、2,2′−ア
ゾビス(4−メトキシ−2,4−ジメチルバレロニトリ
ル)、ジメチル−2,2′−アゾビスイソブチレート、
2,2′−アゾビス(2−メチルブチロニトリル)、1
,1′−アゾビス(1−シクロヘキサンカルボニトリル
)等のアゾ化合物が好適である。また、t−ブチルペル
オクトアート、ジクミルペルオキシド、ジ−t−ブチル
ペルオキシド、ジベンゾイルペルオキシド等の有機過酸
化物を使用することもできる。これら重合開始剤は、モ
ノマー混合物に対し 0.001〜2.0 モル%、特
に0.01〜1.0 モル%用いるのが好ましい。 【0016】重合は、通常30〜100℃、好ましくは
50〜80℃で1〜10時間行なわれ、使用するラジカ
ル重合開始剤、モノマー溶剤の種類などにより適宜選定
される。また、重合は窒素等の不活性ガス雰囲気下で行
なうのが好ましい。 【0017】重合後、反応液から再沈澱、溶剤留去など
、公知の方法により共重合体を単離することができる。 また、得られた共重合体は、再沈澱を繰返したり、膜分
離、クロマトグラフ法、抽出法などにより未反応のモノ
マー等を除去して精製することができる。 【0018】このようにして得られる本発明のシリコー
ン/(メタ)アクリル酸共重合体は、優れた被膜形成能
を有するのみならず、表面摩擦力が非常に小さいため、
各種の化粧料に配合して、優れた感触、整髪力、セット
保持力及び潤滑性等を付与することができる。また、優
れた増粘性を有するため、各種クリーム状、ゲル状等の
形態の化粧料に増粘剤として配合することもできる。さ
らに水溶性に優れるため、水系基剤に用い易く、またシ
ャンプー、皮膚洗浄剤等で容易に除去できる。 【0019】本発明の化粧料は、前記シリコーン/(メ
タ)アクリル酸共重合体を配合し、通常の方法に従って
製造することができ、例えばヘアスプレー、セットフォ
ーム、セットローション、ジェル、シャンプー、リンス
、マニキュア、マスカラ等として、水溶液、水性アルコ
ール溶液、乳濁液、クリーム、ゲル等の剤形で適用する
ことができる。 【0020】これらのうち、噴射剤を用いる毛髪化粧料
においては、原液中に本発明のシリコーン/(メタ)ア
クリル酸共重合体を0.01〜15%、好ましくは 0
.1〜6%;エタノール等の低級アルコール類、ポリオ
ール類、水などの溶剤を50〜99.8%;炭化水素類
、エステル油類、シリコーン及びその誘導体、天然油脂
などの油剤を 0.1〜20%配合するのが好ましい。 また、必要に応じて高級アルコール類、ミリスチン酸オ
クチルドデシル、グリセリン、ポリエチレングリコール
、ポリオキシエチレンヘキサデシルエーテル等の感触向
上剤を 0.5〜3.0 %、ポリオキシエチレンステ
アリルエーテル等のカチオン性高分子などの被膜形成助
剤を 0.1〜3.0 %併用することもできる。さら
に本発明共重合体以外の公知の整髪性ポリマーを配合す
ることもできる。なお、噴射剤としては、LPG 、フ
ロンガス、ジメチルエーテルなどの液化ガス及びCO2
 、N2などの圧縮ガスなどを1種又は2種以上用いる
ことができる。 【0021】また、ヘアセットジェルなどのゲル状毛髪
化粧料においては、シリコーン/(メタ)アクリル酸共
重合体を 0.5〜10.0%、好ましくは 1.0〜
3.0 %、他の整髪性ポリマーを0〜10.0%、ポ
リアクリル酸、ヒドロキシエチルセルロース等の水溶性
高分子を増粘剤として 0.5〜2.0 %配合するの
が好ましく、これに精製水及び所望により低級アルコー
ルを加えた溶剤を用いるのが好ましい。また、従来汎用
されている水溶性高分子と併用することによりさらに感
触を向上させることができる。 【0022】その他、シャンプー、リンス等の毛髪化粧
料には、本発明のシリコーン/(メタ)アクリル酸共重
合体を 0.1〜5.0 %、特に 0.5〜2.0 
%配合するのが好ましい。 【0023】また、マスカラ、マニキュア等においては
、本発明のシリコーン/(メタ)アクリル酸共重合体を
 0.001〜10.0%配合するのが好ましい。 【0024】なお、本発明の化粧料には、通常用いられ
ている防腐剤、紫外線吸収剤、金属イオン封鎖剤、抗フ
ケ剤等の薬効剤や、色素、香料などを目的に応じて添加
することもできる。 【0025】 【発明の効果】本発明のシリコーン/(メタ)アクリル
酸共重合体は、優れた被膜形成能を有し、シリコーンマ
クロマーを含有しているため、被膜表面上に薄いシリコ
ーンの被膜を形成する。この結果、従来の被膜形成樹脂
では得られなかった潤滑性を得ることができ、塗布時の
感触が非常に良好である。このため、従来ゴワつき等を
抑えるために化粧料に配合されていた油剤等の量を減少
させることができ、これにより毛髪化粧料に用いた場合
、被膜形成樹脂の毛髪親和性やセット保持力を低下させ
ることもなく、塗布後のベタつきを低減することもでき
る。さらに、増粘効果を示すことから、これを増粘剤と
して化粧料に配合することにより、化粧料をながれにく
くしたり、成形したときに崩れにくくすることもできる
。また、本発明共重合体を含有する化粧料は、常湿のみ
ならず、高湿度下においても優れた感触及び被膜保持力
を有し、しかも洗浄により容易に洗い落とすことができ
るものである。 【0026】 【実施例】次に実施例を挙げ、本発明をさらに説明する
が、本発明はこれら実施例に限定されるものではない。 【0027】実施例1 還流冷却器、滴下ロート、温度計、窒素ガス導入管及び
攪拌装置を取り付けた四つ口フラスコに窒素ガス導入後
、フラスコを加熱昇温して、1時間窒素置換を行なう。 一方滴下ロート(滴下ロートAと称する)に2,2′−
アゾビスイソブチロニトリル(AIBN)1重量部及び
酢酸エチル10重量部を入れ、もう一方の滴下ロート(
滴下ロートBと称する)にポリジメチルシロキシプロピ
ルメタクリル酸エステル(式(2)中、n=140 )
50重量部、メタクリル酸50重量部及び酢酸エチル1
00重量部を入れた。フラスコを60℃に保った状態で
滴下ロートAの内容物及び滴下ロートBの内容物を4時
間かけて滴下し、重合した。重合後、酢酸エチルにて2
回洗浄して精製し、80℃20mmHgで12時間真空
乾燥した。得られたポリマーは、白色の固体であり、N
MR による重合体の組成比は、ジメチルシロキサン:
メタクリル酸=46:54であり、GPC によるポリ
スチレン換算重量平均分子量は約113000であった
。 【0028】実施例2 還流冷却器、滴下ロート、温度計、窒素ガス導入管及び
攪拌装置を取り付けた四つ口フラスコに窒素ガス導入後
、フラスコを加熱昇温して、1時間窒素置換を行なう。 一方滴下ロート(滴下ロートAと称する)にAIBN5
重量部及び酢酸エチル10重量部を入れ、もう一方の滴
下ロート(滴下ロートBと称する)にポリジメチルシロ
キシプロピルメタクリル酸エステル(式(2)中、n=
140 )30重量部、メタクリル酸70重量部及び酢
酸エチル100重量部を入れた。フラスコを60℃に保
った状態で滴下ロートAの内容物及び滴下ロートBの内
容物を4時間かけて滴下し、重合した。重合後、酢酸エ
チルにて2回洗浄して精製し、80℃20mmHgで1
2時間真空乾燥した。得られたポリマーは、白色の固体
であり、NMR による重合体の組成比は、ジメチルシ
ロキサン:メタクリル酸=29:71であり、GPC 
によるポリスチレン換算重量平均分子量は約54000
であった。 【0029】試験例1 本発明のシリコーン/(メタ)アクリル酸共重合体及び
市販の整髪剤用被膜形成樹脂(ポリビニルピロリドン)
について、すべり、高湿度下でのセットの崩れ難さを感
触評価した。結果を表1に示す。 (試料)本発明共重合体A:メタクリル酸/ポリシロキ
シルプロピルメタクリル酸エステル(式(2)中、n=
140 )=46/54(%) 本発明共重合体B:メタクリル酸/ポリシロキシルプロ
ピルメタクリル酸エステル(式(2)中、n=140 
)=24/76(%) 【0030】(試験方法) (1)セット保持力 長さ18cm、重さ1.5gの毛束を水でぬらし、タオ
ルドライ後、ポリマー2%(50%KOH 中和)エタ
ノール溶液を2g塗布し、直径2cmのロッドに巻いて
自然乾燥させた。乾燥後、カールのついた毛髪からロッ
ドをはずした。これを、恒湿箱(20℃、98%RH)
に30分間つるし、カールの伸びを観察し、セット保持
力を以下の基準で判断した。この結果を表1に示す。 (2)すべり性 長さ18cm重さ10gの毛束を水でぬらし、タオルド
ライ後ポリマー2%(50%KOH 中和)エタノール
溶液を0.2g塗布し、自然乾燥させた。これについて
以下の基準で専門パネラー10名により感触評価を行っ
た。 ◎:たいへん良い ○:良い △:普通 ×:悪い 【0031】 【表1】 【0032】実施例3  ミスト:下記成分を混合して
、ミストを製造した。 (成分)                     
                       (%
)本発明共重合体A(試験例1と同じ)       
            3.0両性ポリマー(ユカフ
ォーマーM75* )               
   1.0非イオン性活性剤(グリセルイソステアレ
ート)         0.5エタノール     
                         
            適量香料         
                         
              微量計        
                         
                100.0  *:
ダイヤケムコ社製 【0033】実施例4  ブロー剤:下記成分を混合し
て、ブロー剤を製造した。 (成分)                     
                       (%
)本発明共重合体B(試験例1と同じ)       
            0.5香料        
                         
               微量エタノール   
                         
              10.0精製水    
                         
                 適量  計   
                         
                     100.
0  【0034】実施例5  シャンプー剤:下記成
分を混合して、毛髪用シャンプーを製造した。 (成分)                     
                       (%
)ラウリルポリオキシエチレン硫酸エステルトリエタノ
ールアミン塩(40%水溶液)           
   32.0ラウロイルジエタノールアミド    
                     3.0ポ
リエチレングリコール               
                1.0本発明共重合
体B(試験例1と同じ)              
     1.0精製水              
                         
       適量香料              
                         
         微量  計           
                         
             100.0【0035】実
施例6  フォーム剤:下記成分を混合して、フォーム
剤を製造した。 (成分)                     
                         
(%)本発明共重合体B(試験例1と同じ)     
                3.5非イオン性界
面活性剤(ソフタノール90,日本触媒製)    1
.0香料                     
                         
    微量エタノール              
                         
      2.0精製水             
                         
          適量液化石油ガス       
                         
           7.0  計        
                         
                  100.0【0
036】試験例2 実施例6及び市販のヘアフォームA(被膜形成樹脂とし
てポリビニルピロリドン(PVP)/酢酸ビニル(VA
c)=6/4を使用)について感触による性能評価を行
なった。結果を表2に示す。 (試験方法)実験用人頭モデル(ウィッグ)2組の毛髪
を水でぬらした後、実施例6及び市販のヘアフォームA
をそれぞれ2g塗布し、直径2cmのロッドに巻いて自
然乾燥させた。乾燥後、毛髪からロッドをはずし、すべ
り、セット力を専門パネラー10名により評価した。こ
の後、恒湿箱(20℃、98%RH)に30分間放置し
、セットのくずれを観察した。このウィッグをシャンプ
ーで洗浄し、洗い落ちやすさを評価した。 ◎:たいへん良い ○:良い △:普通 ×:悪い 【0037】 【表2】
Detailed Description of the Invention [0001] [Industrial Application Field] The present invention provides a novel silicone/(meth)acrylic acid copolymer having excellent film-forming properties, lubricity, thickening properties, etc., and a silicone/(meth)acrylic acid copolymer containing the same. Regarding cosmetics. BACKGROUND OF THE INVENTION The demands placed on cosmetics have become higher, and various film-forming agents have come to be used in order to generally impart good properties to cosmetic films. Especially hairspray
In hair cosmetics such as setting lotions, hair styling ability,
A film-forming resin is blended for the purpose of imparting set holding power and the like. Conventionally, polyvinylpyrrolidone, polyvinylpyrrolidone/vinyl acetate copolymer, vinyl acetate/crotonic acid copolymer, etc. have been used as the film-forming resin. Further, JP-A-2-25411 describes a cosmetic composition using a copolymer mainly composed of a silicone compound and an acrylate as a film-forming agent, and discloses that it forms a moisture-resistant film. Further, various skin and hair cosmetics contain thickeners depending on the dosage form, and various water-soluble polymer substances are used as the thickeners. [0003] Problems to be Solved by the Invention [0003] However, although film-forming resins conventionally blended into hair cosmetics have a certain degree of set-holding power when used normally, they do not hold well under high humidity conditions. Due to moisture absorption, it became more sticky and more fluid, and could not maintain the hair set sufficiently. Although the copolymer disclosed in JP-A-2-25411 has improved setting properties at high humidity, it requires a hydrocarbon such as isoparaffin, volatile silicone, etc. as a solvent, and has poor water solubility. Hair cosmetics must be easily removed by shampooing, requiring water solubility on the one hand and low hygroscopicity on the other hand. It is difficult to simultaneously satisfy these contradictory requirements, and in the past, water solubility has often been abandoned and other solvents or solvent mixtures have been used, as described above. [0004] Furthermore, setting agents such as hair sprays contain large amounts of oils and active agents in order to prevent the hair from becoming stiff or coarse after drying. The combination of these oils and active agents reduces the affinity of the film-forming resin for hair.
This has caused problems such as a decrease in the ability of the hair to hold the hair set, and also a sticky feeling caused by hand-applying the oil or activator after application to the hair. Furthermore, there are also problems such as peeling of the resin coating on the hair surface due to brushing or the like, ie, so-called flaking, which deteriorates the luster of the hair. Incidentally, this flaking was often caused by the water-soluble polymeric substance blended as a thickener. [0005] Therefore, not only film forming properties but also lubricity,
A new polymer with thickening properties, and blending it,
There has been a desire for a cosmetic that has a good feel when applied, and has excellent hair styling and set holding power, especially when applied to hair, even under high humidity. [Means for Solving the Problems] Under these circumstances, the present inventors conducted intensive research and found that silicone/(meth)acrylic acid or its salt and a silicone macromer are obtained by polymerizing silicone macromer. Acrylic acid copolymers have excellent properties such as film-forming ability, lubricity, and thickening properties, and cosmetics containing them have a very good feel when applied and do not become sticky even under high humidity. The present invention was completed based on the discovery that the hair has a low amount of moisture, suppresses hygroscopicity, and has excellent hair styling and set holding power. That is, the present invention provides (a) and (b) (
a) (meth)acrylic acid or its salt (b) represented by the formula (1) [In the formula, R1 represents a hydrogen atom or a methyl group]
Formula (2) [0011] [In the formula, X represents a radically polymerizable group, and R
2, R3, R4, R5 and R6 may be the same or different and represent a methyl group, an alkoxyl group, an optionally substituted phenyl group, or an optionally substituted phenoxyl group, and m is 1 to 10. silicone/(meth)acrylic acid copolymer obtained by polymerizing a silicone macromer represented by the following integer, n is an integer from 5 to 150] in the presence of a radical polymerization initiator, and the copolymer. The purpose is to provide cosmetics that (a) used in the production of the copolymer of the present invention
The salts of the (meth)acrylic acid component include inorganic salts represented by alkali metal salts such as sodium salts and potassium salts;
Examples include organic salts represented by quaternary ammonium salts. These (a) components can be used alone or in combination of two or more, and can be used in an amount of 10 to 95% by weight (
(hereinafter simply expressed as "%"), particularly preferably from 40 to 80%. [0013] The silicone malokumer as the component (b) is represented by the above formula (2), in which the radically polymerizable group represented by X includes a vinyl group, (meth)acryloyl group, vinylbenzyl group, styryl group, (meth)acrylamide group, vinyl ether group, vinyl ester group, etc. Specific examples of these silicone macromers include:
Polydimethylsiloxypropyl (meth)acrylic acid ester, polydimethylsiloxypropyl vinyl benzyl ether, polymethylphenylsiloxypentene, polydimethylsiloxypropyl (meth)acrylamide, polydimethylsiloxypropyl vinyl benzylate, polymethylphenylsiloxyethoxyethylene, etc. Among these, polydimethylsiloxypropyl (meth)acrylic acid ester, polydimethylsiloxypropyl (meth)acrylamide, etc. are particularly preferred. These (b)
The components can be used alone or in combination of two or more, and it is preferably used in an amount of 5 to 90%, particularly 20 to 60%, of the total monomers. The silicone/(meth)acrylic acid copolymer of the present invention is produced by combining the above components (a) and (b), and performing bulk polymerization, solution polymerization, or suspension polymerization in the presence of a radical polymerization initiator. It is produced by polymerization using a known polymerization method such as a polymerization method or an emulsion polymerization method. At this time, monomers other than the above two types of monomers may be copolymerized within a range that does not impair the effects of the present invention. Among these, it is particularly advantageous to produce by solution polymerization. The solvent used in the solution polymerization method is preferably a polar organic solvent, and a water-miscible organic solvent can also be used in combination with water. Examples of such organic solvents include aliphatic alcohols having 1 to 3 carbon atoms such as methanol, ethanol, and propanol; ketones such as acetone and methyl ethyl ketone;
Among these, methanol, ethanol, acetone, or a mixture of these and water is particularly preferred. These organic solvents can be used alone or in combination of two or more. Examples of radical polymerization initiators include 2,
2'-azobisisobutyronitrile, 2,2'-azobis(2,4-dimethylvaleronitrile), 2,2'-azobis(4-methoxy-2,4-dimethylvaleronitrile), dimethyl-2, 2'-azobisisobutyrate,
2,2'-azobis(2-methylbutyronitrile), 1
, 1'-azobis(1-cyclohexanecarbonitrile) and the like are preferred. Moreover, organic peroxides such as t-butyl peroctoate, dicumyl peroxide, di-t-butyl peroxide, and dibenzoyl peroxide can also be used. These polymerization initiators are preferably used in an amount of 0.001 to 2.0 mol%, particularly 0.01 to 1.0 mol%, based on the monomer mixture. [0016] Polymerization is usually carried out at 30 to 100°C, preferably 50 to 80°C, for 1 to 10 hours, and is appropriately selected depending on the type of radical polymerization initiator and monomer solvent used. Further, the polymerization is preferably carried out under an inert gas atmosphere such as nitrogen. After the polymerization, the copolymer can be isolated from the reaction solution by known methods such as reprecipitation and solvent distillation. Further, the obtained copolymer can be purified by repeating reprecipitation or by removing unreacted monomers and the like by membrane separation, chromatography, extraction, etc. The silicone/(meth)acrylic acid copolymer of the present invention thus obtained not only has an excellent film-forming ability but also has a very small surface frictional force.
It can be blended into various cosmetics to impart excellent feel, hair styling ability, set retention ability, lubricity, etc. Furthermore, since it has excellent thickening properties, it can be incorporated as a thickening agent into various cream-like, gel-like, and other cosmetics. Furthermore, since it has excellent water solubility, it can be easily used in aqueous bases and can be easily removed with shampoos, skin cleansers, etc. The cosmetic of the present invention can be produced by blending the silicone/(meth)acrylic acid copolymer according to a conventional method, such as hair spray, setting foam, setting lotion, gel, shampoo, and conditioner. , nail polish, mascara, etc., in the form of aqueous solutions, hydroalcoholic solutions, emulsions, creams, gels, etc. Among these, in hair cosmetics using a propellant, the silicone/(meth)acrylic acid copolymer of the present invention is contained in the stock solution in an amount of 0.01 to 15%, preferably 0.
.. 1 to 6%; 50 to 99.8% of lower alcohols such as ethanol, polyols, and solvents such as water; 0.1 to 99.8% of solvents such as hydrocarbons, ester oils, silicones and their derivatives, and natural oils and fats. It is preferable to mix 20%. In addition, if necessary, 0.5 to 3.0% of higher alcohols, tactile enhancers such as octyldodecyl myristate, glycerin, polyethylene glycol, polyoxyethylene hexadecyl ether, and cationic agents such as polyoxyethylene stearyl ether may be added. A film forming aid such as a polymer can also be used in an amount of 0.1 to 3.0%. Furthermore, known hair styling polymers other than the copolymer of the present invention can also be blended. In addition, as a propellant, LPG, chlorofluorocarbon gas, liquefied gas such as dimethyl ether, and CO2
, N2, and other compressed gases may be used alone or in combination of two or more. [0021] Furthermore, in gel-like hair cosmetics such as hair setting gels, silicone/(meth)acrylic acid copolymer is contained in an amount of 0.5 to 10.0%, preferably 1.0 to 10.0%.
3.0%, other hair styling polymers from 0 to 10.0%, and water-soluble polymers such as polyacrylic acid and hydroxyethyl cellulose as thickeners from 0.5 to 2.0%. It is preferable to use a solvent prepared by adding purified water and, if desired, a lower alcohol. In addition, the feel can be further improved by using it in combination with conventionally widely used water-soluble polymers. In addition, hair cosmetics such as shampoos and conditioners contain the silicone/(meth)acrylic acid copolymer of the present invention in an amount of 0.1 to 5.0%, particularly 0.5 to 2.0%.
% is preferable. Furthermore, in mascara, nail polish, etc., it is preferable to blend the silicone/(meth)acrylic acid copolymer of the present invention in an amount of 0.001 to 10.0%. [0024] The cosmetics of the present invention may contain commonly used medicinal agents such as preservatives, ultraviolet absorbers, sequestering agents, anti-dandruff agents, pigments, fragrances, etc., depending on the purpose. You can also do that. Effects of the Invention The silicone/(meth)acrylic acid copolymer of the present invention has excellent film-forming ability and contains silicone macromer, so it is possible to form a thin silicone film on the surface of the film. Form. As a result, it is possible to obtain lubricity that could not be obtained with conventional film-forming resins, and the coating feels very good when applied. For this reason, it is possible to reduce the amount of oils, etc. that are conventionally blended into cosmetics to suppress stiffness, etc., and when used in hair cosmetics, the film-forming resin's hair affinity and set retention It is also possible to reduce stickiness after application without reducing the viscosity. Furthermore, since it exhibits a thickening effect, it can be added to cosmetics as a thickener to make the cosmetics difficult to run or crumble when molded. Furthermore, cosmetics containing the copolymer of the present invention have excellent feel and film retention not only under normal humidity but also under high humidity, and can be easily washed off. [Examples] Next, the present invention will be further explained with reference to Examples, but the present invention is not limited to these Examples. Example 1 After introducing nitrogen gas into a four-necked flask equipped with a reflux condenser, dropping funnel, thermometer, nitrogen gas inlet tube, and stirring device, the flask was heated to raise its temperature and replaced with nitrogen for 1 hour. . On the other hand, the dropping funnel (referred to as dropping funnel A) has 2,2'-
Add 1 part by weight of azobisisobutyronitrile (AIBN) and 10 parts by weight of ethyl acetate to the other dropping funnel (
Polydimethylsiloxypropyl methacrylate ester (n=140 in formula (2)) was added to the dropping funnel (referred to as dropping funnel B).
50 parts by weight, 50 parts by weight of methacrylic acid and 1 part by weight of ethyl acetate
00 parts by weight were added. While keeping the flask at 60° C., the contents of dropping funnel A and dropping funnel B were added dropwise over 4 hours to polymerize. After polymerization, 2
It was purified by washing twice and vacuum-dried at 80° C. and 20 mmHg for 12 hours. The resulting polymer is a white solid, N
The composition ratio of the polymer according to MR is dimethylsiloxane:
The ratio of methacrylic acid was 46:54, and the weight average molecular weight in terms of polystyrene by GPC was about 113,000. Example 2 After introducing nitrogen gas into a four-necked flask equipped with a reflux condenser, dropping funnel, thermometer, nitrogen gas inlet tube, and stirring device, the flask was heated to raise its temperature and replaced with nitrogen for 1 hour. . On the other hand, put AIBN5 into the dropping funnel (referred to as dropping funnel A).
parts by weight and 10 parts by weight of ethyl acetate, and into the other dropping funnel (referred to as dropping funnel B) polydimethylsiloxypropyl methacrylate (in formula (2), n=
140), 70 parts by weight of methacrylic acid, and 100 parts by weight of ethyl acetate. While keeping the flask at 60° C., the contents of dropping funnel A and dropping funnel B were added dropwise over 4 hours to polymerize. After polymerization, it was purified by washing twice with ethyl acetate, and then heated at 80°C and 20mmHg for 1 time.
It was vacuum dried for 2 hours. The obtained polymer was a white solid, and the composition ratio of the polymer according to NMR was dimethylsiloxane:methacrylic acid = 29:71, and the composition ratio of the polymer was determined by GPC.
The weight average molecular weight in terms of polystyrene is approximately 54,000
Met. Test Example 1 Silicone/(meth)acrylic acid copolymer of the present invention and commercially available film-forming resin for hair styling agent (polyvinylpyrrolidone)
A tactile evaluation was conducted for slippage and resistance to collapse of the set under high humidity. The results are shown in Table 1. (Sample) Copolymer A of the present invention: methacrylic acid/polysiloxylpropyl methacrylate (in formula (2), n=
140 ) = 46/54 (%) Copolymer B of the present invention: methacrylic acid/polysiloxylpropyl methacrylate (in formula (2), n = 140
) = 24/76 (%) 0030 (Test method) (1) Set retention Wet a hair bundle with a length of 18 cm and a weight of 1.5 g with water, towel dry it, and then dry it with 2% polymer (in 50% KOH). 2 g of ethanol solution was applied, wound around a rod with a diameter of 2 cm, and air-dried. After drying, the rod was removed from the curled hair. Place this in a constant humidity box (20℃, 98%RH)
The curls were hung for 30 minutes, the curls were observed for elongation, and the set holding power was judged based on the following criteria. The results are shown in Table 1. (2) Smoothness A hair bundle with a length of 18 cm and a weight of 10 g was wetted with water, towel-dried, and then 0.2 g of a 2% polymer (neutralized with 50% KOH) ethanol solution was applied and air-dried. This was evaluated by 10 expert panelists according to the following criteria. ◎: Very good ○: Good △: Average ×: Bad 0031 [Table 1] Example 3 Mist: The following components were mixed to produce a mist. (component)
(%
) Copolymer A of the present invention (same as Test Example 1)
3.0 amphoteric polymer (Yukaformer M75*)
1.0 Nonionic activator (glycer isostearate) 0.5 Ethanol

Appropriate amount of fragrance

trace meter

100.0 *:
Manufactured by Diachemco Co., Ltd. Example 4 Blowing agent: A blowing agent was prepared by mixing the following components. (component)
(%
) Copolymer B of the present invention (same as Test Example 1)
0.5 fragrance

trace amount of ethanol

10.0 Purified water

Appropriate amount total

100.
Example 5 Shampoo: A hair shampoo was prepared by mixing the following ingredients. (component)
(%
) Lauryl polyoxyethylene sulfate triethanolamine salt (40% aqueous solution)
32.0 lauroyl diethanolamide
3.0 polyethylene glycol
1.0 Copolymer B of the present invention (same as Test Example 1)
1.0 purified water

Appropriate amount of fragrance

Trace amount meter

Example 6 Foam agent: A foam agent was prepared by mixing the following components. (component)

(%) Copolymer B of the present invention (same as Test Example 1)
3.5 Nonionic surfactant (Softanol 90, manufactured by Nippon Shokubai) 1
.. 0 fragrance

trace amount of ethanol

2.0 Purified water

Appropriate amount of liquefied petroleum gas

7.0 total

100.0 0
Test Example 2 Example 6 and commercially available hair foam A (polyvinylpyrrolidone (PVP)/vinyl acetate (VA) as film-forming resin)
c) = 6/4) was evaluated by touch. The results are shown in Table 2. (Test method) After wetting the hair of two sets of experimental human head models (wigs) with water, Example 6 and commercially available hair foam A
2 g of each was applied, wound around a rod with a diameter of 2 cm, and air-dried. After drying, the rod was removed from the hair, and ten expert panelists evaluated the sliding and setting power. Thereafter, the set was left in a constant humidity box (20° C., 98% RH) for 30 minutes, and the set was observed for deterioration. This wig was washed with shampoo and the ease with which it was washed off was evaluated. ◎: Very good ○: Good △: Average ×: Bad 0037] [Table 2]

Claims (2)

【特許請求の範囲】[Claims] 【請求項1】  (a)及び(b) (a)式(1) 【化1】 〔式中、R1は水素原子又はメチル基を示す〕で表わさ
れる(メタ)アクリル酸又はその塩 (b)式(2) 【化2】 〔式中、Xはラジカル重合性基を示し、R2、R3、R
4、R5及びR6は同一又は異なってもよく、メチル基
、アルコキシル基、置換されていてもよいフェニル基又
は置換されていてもよいフェノキシル基を示し、mは1
〜10の整数を示し、nは5〜150の整数を示す〕で
表わされるシリコーンマクロマーをラジカル重合開始剤
の存在下に重合させて得られるシリコーン/(メタ)ア
クリル酸共重合体。
Claim 1: (a) and (b) (a) Formula (1) (meth)acrylic acid or its salt (b ) Formula (2) [Formula, X represents a radically polymerizable group, R2, R3, R
4, R5 and R6 may be the same or different and represent a methyl group, an alkoxyl group, an optionally substituted phenyl group, or an optionally substituted phenoxyl group, and m is 1
10, n is an integer of 5 to 150] in the presence of a radical polymerization initiator.
【請求項2】  請求項1記載のシリコーン/(メタ)
アクリル酸共重合体を含有する化粧料。
[Claim 2] The silicone/(meth) according to Claim 1.
A cosmetic containing an acrylic acid copolymer.
JP13478391A 1991-06-06 1991-06-06 New copolymer and cosmetic containing same Pending JPH04359912A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP13478391A JPH04359912A (en) 1991-06-06 1991-06-06 New copolymer and cosmetic containing same

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP13478391A JPH04359912A (en) 1991-06-06 1991-06-06 New copolymer and cosmetic containing same

Publications (1)

Publication Number Publication Date
JPH04359912A true JPH04359912A (en) 1992-12-14

Family

ID=15136452

Family Applications (1)

Application Number Title Priority Date Filing Date
JP13478391A Pending JPH04359912A (en) 1991-06-06 1991-06-06 New copolymer and cosmetic containing same

Country Status (1)

Country Link
JP (1) JPH04359912A (en)

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US5653969A (en) * 1996-03-21 1997-08-05 The Procter & Gamble Company Low residue hair care compositions
US5653968A (en) * 1996-03-21 1997-08-05 The Proctor & Gamble Company Rinse-off hair care compositions
US5658557A (en) * 1989-08-07 1997-08-19 The Procter & Gamble Company Hair care compositions comprising silicone-containing copolymers
US5665337A (en) * 1996-03-21 1997-09-09 The Procter & Gamble Company Low residue hair care compositions using grafted copolymers
US5667771A (en) * 1996-03-21 1997-09-16 The Procter & Gamble Company Rinse-off hair care compositions using grafted copolymers
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US5911979A (en) * 1995-01-09 1999-06-15 The Procter & Gamble Company Aqueous hair setting composition containing silicone grafted copolymer
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US5658557A (en) * 1989-08-07 1997-08-19 The Procter & Gamble Company Hair care compositions comprising silicone-containing copolymers
US5997853A (en) * 1989-08-07 1999-12-07 The Procter & Gamble Hair conditioning and styling compositions
US5618524A (en) * 1989-08-07 1997-04-08 The Procter & Gamble Company Hair conditioning and styling compositions
US5911979A (en) * 1995-01-09 1999-06-15 The Procter & Gamble Company Aqueous hair setting composition containing silicone grafted copolymer
EP0779318A1 (en) 1995-12-14 1997-06-18 Wako Pure Chemical Industries, Ltd. Silicon-containing block copolymer
US5760136A (en) * 1995-12-14 1998-06-02 Wako Pure Chemical Industries, Ltd. Silicon-containing block copolymer
US5653969A (en) * 1996-03-21 1997-08-05 The Procter & Gamble Company Low residue hair care compositions
US5653968A (en) * 1996-03-21 1997-08-05 The Proctor & Gamble Company Rinse-off hair care compositions
US5665337A (en) * 1996-03-21 1997-09-09 The Procter & Gamble Company Low residue hair care compositions using grafted copolymers
US5667771A (en) * 1996-03-21 1997-09-16 The Procter & Gamble Company Rinse-off hair care compositions using grafted copolymers
US5916548A (en) * 1996-09-04 1999-06-29 The Procter & Gamble Company Personal care compositions
US5830447A (en) * 1996-09-04 1998-11-03 The Procter & Gamble Company Personal care compositions
US5804173A (en) * 1996-09-04 1998-09-08 The Procter & Gamble Company Personal care compositions
US5863527A (en) * 1996-09-04 1999-01-26 The Proctor & Gamble Company Personal care compositions
US6136296A (en) * 1997-04-25 2000-10-24 The Procter & Gamble Company Personal care compositions
US6555117B2 (en) 1997-04-25 2003-04-29 The Procter & Gamble Company Personal care compositions containing linear toughened silicone grafted polymers
US6074628A (en) * 1997-04-25 2000-06-13 Procter & Gamble Hairspray compositions containing silicon block copolymers
US6113883A (en) * 1997-04-25 2000-09-05 The Procter & Gamble Company Hair styling compositions comprising silicone-containing copolymers
US6165457A (en) * 1997-05-12 2000-12-26 The Procter & Gamble Company Personal care compositions containing toughened grafted polymers
US6106820A (en) * 1997-05-12 2000-08-22 Procter & Gamble Company Cosmetic compositions
US5929173A (en) * 1997-05-12 1999-07-27 The Procter & Gamble Company Toughened grafted polymers
EP1604632A1 (en) * 2004-06-08 2005-12-14 Shiseido Co., Ltd. Cosmetic comprising a specific terpolymer
WO2019003898A1 (en) * 2017-06-28 2019-01-03 東レ・ダウコーニング株式会社 Film-forming agent for cosmetics and cosmetics containing same
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