JPH0144165B2 - - Google Patents
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- Publication number
- JPH0144165B2 JPH0144165B2 JP19697485A JP19697485A JPH0144165B2 JP H0144165 B2 JPH0144165 B2 JP H0144165B2 JP 19697485 A JP19697485 A JP 19697485A JP 19697485 A JP19697485 A JP 19697485A JP H0144165 B2 JPH0144165 B2 JP H0144165B2
- Authority
- JP
- Japan
- Prior art keywords
- carbon atoms
- fatty acid
- oil
- solid
- saturated
- 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
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11C—FATTY ACIDS FROM FATS, OILS OR WAXES; CANDLES; FATS, OILS OR FATTY ACIDS BY CHEMICAL MODIFICATION OF FATS, OILS, OR FATTY ACIDS OBTAINED THEREFROM
- C11C3/00—Fats, oils, or fatty acids by chemical modification of fats, oils, or fatty acids obtained therefrom
- C11C3/04—Fats, oils, or fatty acids by chemical modification of fats, oils, or fatty acids obtained therefrom by esterification of fats or fatty oils
- C11C3/08—Fats, oils, or fatty acids by chemical modification of fats, oils, or fatty acids obtained therefrom by esterification of fats or fatty oils with fatty acids
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
- A61K8/34—Alcohols
- A61K8/345—Alcohols containing more than one hydroxy group
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
- A61K8/37—Esters of carboxylic acids
- A61K8/375—Esters of carboxylic acids the alcohol moiety containing more than one hydroxy group
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/63—Steroids; Derivatives thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q1/00—Make-up preparations; Body powders; Preparations for removing make-up
- A61Q1/02—Preparations containing skin colorants, e.g. pigments
- A61Q1/04—Preparations containing skin colorants, e.g. pigments for lips
- A61Q1/06—Lipsticks
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q1/00—Make-up preparations; Body powders; Preparations for removing make-up
- A61Q1/02—Preparations containing skin colorants, e.g. pigments
- A61Q1/10—Preparations containing skin colorants, e.g. pigments for eyes, e.g. eyeliner, mascara
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q1/00—Make-up preparations; Body powders; Preparations for removing make-up
- A61Q1/12—Face or body powders for grooming, adorning or absorbing
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11C—FATTY ACIDS FROM FATS, OILS OR WAXES; CANDLES; FATS, OILS OR FATTY ACIDS BY CHEMICAL MODIFICATION OF FATS, OILS, OR FATTY ACIDS OBTAINED THEREFROM
- C11C3/00—Fats, oils, or fatty acids by chemical modification of fats, oils, or fatty acids obtained therefrom
- C11C3/04—Fats, oils, or fatty acids by chemical modification of fats, oils, or fatty acids obtained therefrom by esterification of fats or fatty oils
- C11C3/10—Ester interchange
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
- A61K2800/80—Process related aspects concerning the preparation of the cosmetic composition or the storage or application thereof
- A61K2800/87—Application Devices; Containers; Packaging
- A61K2800/872—Pencils; Crayons; Felt-tip pens
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Birds (AREA)
- Epidemiology (AREA)
- Organic Chemistry (AREA)
- Wood Science & Technology (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- General Chemical & Material Sciences (AREA)
- Emergency Medicine (AREA)
- Cosmetics (AREA)
Description
〔産業上の利用分野〕
本発明は使用感及び化粧もちが共に優れた固型
化粧料に関するものである。
〔従来の技術〕
固型化粧料としては、代表的なものに口紅、リ
ツプクリーム、フアンデーシヨンステイツク、チ
ツクなどの棒状化粧料、アイブロウベンシル、ア
イライナーペンシルのようなペンシル型化粧料、
フアンデーシヨン、アイシヤドウ、頬紅などのプ
レスドパウダー及び油性のケーキ状化粧料があ
る。
これらのうち油性化粧料は従来カルナウバワツ
クス、キヤンデリラワツクス、セレシン、マイク
ロクリスタリンワツクス、硬化動植物脂、ミツロ
ウなどの固体脂とヒマシ油、オリーブ油、ホホバ
油、スクワラン、各種合成エステル油、シリコー
ンオイル、流動パラフイン、ワセリンなどの液体
又は半液状油の混合系に粉体を分散せしめたもの
である。
これらの従来使用されてきた油分を組み合わせ
て上述の如き固型化粧料を製造しようとした場
合、固体脂と液体又は半液状油の割合を調節する
ことにより、製品に必要とされる性能である使用
感及び化粧もちを満足させなければならない。し
かし、この2つを同時に満足させることは困難で
ある。
その理由としては次の如く考えられる。油性化
粧料の組織構造としては、固体脂の結晶が網目構
造を形成し、その網目の中を液体油が満たした組
織構造が一般に考えられており、この網目構造の
強度、柔軟性が化粧料の使用感及び化粧もちに大
きく関与している。即ち固体脂が多い(液体油が
少ない)場合は網目構造が緻密になり組織が強固
のため、化粧もちは良いが、のびが重く、タツチ
もハードになるといつた如く使用感が悪い。反対
に固体脂が少ない(液体油が多い)場合は、網目
構造が粗となり、組織が軟弱のため化粧もちは悪
いが、のびは軽く、タツチもソフトで使用感が良
い。このように化粧料に要求される性能を同時に
満足させることは固体脂と液体油の割合の調節だ
けでは困難であり、また油分の種類を変化させて
も同様である。
例えば、口紅などの棒状化粧料や、アイライナ
ーなどのペンシル型化粧料では、固体脂を減らす
(液体油を増す)と、のびが軽く、タツチもソフ
トで、使用感の良いものが得られるが、化粧もち
については、にじみやすい、色落しちしやすい、
色移りしやすいなどが認められる。反対に固体脂
を増す(液体油を減らす)と、のびが重い、タツ
チがハード、ざらつくなどの使用感の劣化が起こ
るが、化粧もちは良くなる。
またプレストパウダータイプの化粧料は粉体の
比率が多く、使用時の感触、調整及び成形時の結
合又は保型を目的として、前述の如き油成分が用
いられている。この場合、粉体粉子間の結合力が
不充分であると、使用時にくずれたり、耐衝撃性
が低く割れたり、ひび割れを生じたりする。逆に
粉末粒子間の結合力が強すぎるとパフやはけの付
きが悪く、適用が困難であつたり、油性のテカリ
による外観の低下をきたす。こうした現象は固体
脂と液体油の割合の調節、油分の種類の変化及び
プレス圧などの成形条件を調節することだけでは
解決することは困難である。
〔本発明が解決しようとする問題点〕
以上の如く、従来使用されてきた油分の組み合
わせだけで、固型化粧料を製造しようとした場
合、製品に必要な性能である使用感及び化粧もち
並びにその他の望ましい性能を同時に満足させる
ことは困難である。
本発明はかかる従来技術の欠点を解決し、使用
感及び化粧もちの何れをも満足する固型化粧料を
得んとするものである。
〔問題点を解決するための手段〕
本発明者等は先にその組成中に分子中に炭素数
20〜26の飽和直鎖状アシル基及び炭素数16〜22の
不飽和アシル基をそれぞれ少なくとも1つ有する
混酸基トリグリセリドを主体とし、かつ構成脂肪
酸として炭素数20〜26の飽和直鎖脂肪酸及び炭素
数16〜22の不飽和脂肪酸を特定割合で含有する可
塑性油脂を配合すれば優れた固型化粧料が得られ
ることを見出したが(特願昭60−50124号)、本発
明者等は上記可塑性油脂、即ち分子中に炭素数20
〜26の飽和直鎖状アシル基及び炭素数16〜22の不
飽和アシル基をそれぞれ少なくとも1つ有する混
酸基トリグリセリドを主体とし、かつ構成脂肪酸
組成が炭素数20〜26の飽和直鎖脂肪酸30〜70重量
%、好ましくは40〜65重量%、炭素数16〜22の不
飽和脂肪酸20〜60重量%、好ましくは25〜50重量
%である可塑性油脂に、式(1)
(式中、Rは合計11〜23個の炭素原子を含有し、
カルボキシル結合位から主鎖の中心までに、少な
くとも1つのアルキル置換基を有する飽和脂肪族
炭化水素基である。)
で表わされる分岐脂肪酸コレステリルエステルを
配合することにより、上記欠点のない優れた固型
化粧料が得られることを見出した。
本発明によれば、使用感及び化粧もちを同時に
満足させる固型化粧料が提供される。
本発明に使用される可塑性油脂は、これを化粧
料に配合すると、皮膚塗布時ののびが非常に軽
く、タツチもソフトになるなど顕著な使用感改良
効果が認められる。又、化粧もちも或る程度改良
されるが、その改良効果は未だ弱く不満足なもの
であることが見出された。
又、本発明に使用される分岐脂肪酸コレステリ
ルエステルの化粧料への利用については、既に特
開昭56−65809号公報及び特開昭59−1407号公報
に記載されており、化粧料の肌へのなじみを改善
することが示されている。その他、化粧もちにつ
いても或る程度改良されることを認めたが、その
効果は弱く不満足なものであることが見出され
た。
しかるに本発明者等は上記可塑性油脂と共に分
岐脂肪酸コレステリルエステルを固型化粧料に配
合したところ、両者の間に顕著な相剰効果を発見
した。
即ち、これらの成分を個々に配合した場合に比
較して、使用感及び化粧もちが飛躍的に改善され
た固型化粧料が得られることがわかつた。その作
用機構は未だ判明していないが、次の様に推測さ
れる。即ち、可塑性油脂と分岐脂肪酸コレステリ
ルエステルを共に添加することにより、フレキシ
ブルな結晶の網目構造が形成されると考えられ
る。そのため塗布時には網目構造が柔軟であるが
ゆえに適度に組織がこわれ、それによりのびは軽
く、タツチもソフトで良い使用感が得られる。一
方、柔軟な組織であるため塗布後の構造の一部が
破壊されずに残り、この微小な組織の切片は柔軟
であるため皮膚表面に付着しやすく化粧もちが良
いものと考える。
本発明の固型化粧料に含有される上記可塑性油
脂は、好ましくは分子中に2つの飽和直鎖状アシ
ル基を持つ、二飽和−不飽和型の混酸基トリグリ
セリドを主体とするものである。この混酸基トリ
グリセリドの飽和直鎖状アシル基のうち少なくと
も1つが炭素数20〜26のものであり、他の飽和直
鎖状アシル基は炭素数16〜26であり、不飽和アシ
ル基は炭素数16〜22のものである。なかでも2つ
の飽和直鎖状アシル基がいずれも炭素数20〜26で
あるものがより好ましい。可塑性油脂の残りの成
分は炭素数8以上の飽和直鎖状脂肪酸及び/又は
炭素数8以上の不飽和脂肪酸を構成脂肪酸とする
トリグリセリドであり、さらに、それら脂肪酸の
炭素数は16〜24のものであることが好ましい。こ
の時、構成脂肪酸の炭素数が8未満のものは、に
おいが悪い他、加水分解を起こした場合、皮膚刺
激の恐れがある。尚、本発明において、分子中に
炭素数20〜26の飽和直鎖状アシル基及び炭素数16
〜22の不飽和アシル基をそれぞれ少なくとも1つ
有する混酸基トリグリセリドを主体とするとはト
リグリセリド中の最多量成分であることを意味
し、通常可塑性油脂中、上記二飽和一不飽和型の
混酸基トリグリセリドが35%程度以上、好ましく
は45%以上含有されていることをいう。
上記可塑性混酸基トリグリセリドを構成する炭
素数16〜22の不飽和脂肪酸としては、オレイン
酸、リノール酸、リノレイ酸等が挙げられ、その
結合位置はα位、β位いずれでも良いが、その混
合物が好ましい。又、不飽和脂肪酸中の不飽和結
合の位置、及び数に制限はないが、酸化安定性の
面から、不飽和結合の数は1〜2個であることが
好ましい。炭素数20〜26の飽和直鎖状脂肪酸とし
ては、アラキン酸、ベヘン酸等が挙げられるが、
炭素数20〜26の範囲以外の場合、柔軟性に若干欠
けてくる。また炭素数が18以下となると、明らか
に結晶性が高くなり、もろくなるため、固型化粧
料に配合した際、前述の性能が発揮されない。
本発明の固型化粧料中の上記可塑性油脂の含有
量は化粧料の剤型により異なるが、0.1〜80重量
%の範囲で含有することができ、通常0.2〜50重
量%の範囲で含有させるのが好ましい。この範囲
以下では充分な効果が得られず、又この範囲以上
の高濃度では効果が飽和に達し、経済的に不利で
あるばかりか、可塑性油脂自身の物性が化粧料に
発現し、のびが重くなるなど使用感が劣化し、化
粧料の性能が損なわれる。
尚、本発明に使用される可塑性油脂の製法は特
に限定されないが、例えば特開昭60−53598号公
報に記載の如き方法で得られる。
即ち、所定量以上の炭素数20〜26の飽和直鎖状
脂肪酸を含有する炭素数8以上の飽和直鎖状脂肪
酸と所定量以上の炭素数16〜22の不飽和脂肪酸を
含有する炭素数8以上の不飽和脂肪酸とが構成脂
肪酸であるトリグリセリドのエステル交換法、も
しくはそれら脂肪酸とグリセリンとのエステル化
法等により製造することができる。本発明での混
酸基トリグリセリドの純度を上げるためには、得
られたトリグリセリド混合物は溶剤分別等で高融
点部や低融点部を除去することが好ましい。
本発明に使用される分岐脂肪酸コレステリルエ
ステルの製造に用いられる分岐脂肪酸
(RCOOH)は、炭素数12〜24(Rとしての炭素数
として11〜23)のものが使用できるが、炭素数14
〜20(Rとしての炭素数13〜19)のものが好まし
い。
分岐脂肪酸は、カルボキシル基結合位から主鎖
の中央までに少なくとも1つのアルキル置換基を
有する飽和分岐脂肪酸である。このような飽和分
岐脂肪酸は、石油化学工業原料又は油脂化学工業
原料より容易に得られる。
石油化学工業原料より得られるこのような分岐
脂肪酸の例としては、α位に側鎖を有する分岐脂
肪酸があり、次式で表わされる。
(式中、R1及びR2はそれぞれ直鎖又は分岐鎖の
飽和脂肪族炭化水素基であり、R1及びR2の炭素
原子数の和は12〜18である)
α位に側鎖を有する飽和分岐脂肪酸の好ましい
具体例としては、5,7,7−トリメチル−2−
(1,2,3−トリメチルブチル)−オクタン酸、
2−ヘプチルウンデカン酸、2−ヘキシルデカン
酸、2−オクチルドデカン酸、2−ペンチルノナ
ン酸等がある。
油脂化学工業原料より得られる飽和分岐脂肪酸
の例としては、次の式で表わされるメチル分岐鎖
を有する脂肪酸がある。
(式中、mとnの和は14であり、m=n=7を中
心とする分布を有する)
このようなメチル分岐鎖脂肪酸は、例えばオレ
イン酸のダイマー製造時の副生物として得られる
メチル分岐イソステアリン酸であつて、例えばそ
のイソプロエステルとして市販されている(米国
エメリー社など)。
本発明の固型化粧料に含有される分岐脂肪酸コ
レステリルエステルは、上記の分岐脂肪酸又はそ
の誘導体とコレステロールから通常のエステルを
製造する方法によつて製造される。
本発明の固型化粧料中の上記分岐脂肪酸コレス
テリルエステルの含有量は化粧品の剤型により異
なるが、0.01〜50重量%の範囲で含有することが
でき、通常0.03〜30重量%の範囲で含有させるの
が好ましい。この範囲以下の低濃度では充分な効
果が得られず、又この範囲以上の高濃度を配合し
ても、効果が既に飽和に達しており、経済的な面
からも不利であり、また分岐脂肪酸コレステリル
エステル自身の物性が発現し、べたつきが目立つ
などの問題が起こりやすくなる。
尚、本発明における分岐脂肪酸コレステリルエ
ステルの製法については、特開昭56−65900号公
報に記載されているが、本発明の固型化粧料に使
用される分岐脂肪酸コレステリルエステルの製法
はこれに制限されるものではない。
本発明の固型化粧料(棒状化粧料)の製造は、
当該化粧料組成中に上記各成分を夫々の配合量で
含有させる以外は常法に従い行われる。即ち、上
記量の可塑性油脂及び分岐脂肪酸コレステリルエ
ステルと油脂類、ワツクス、ロウ等の油性基剤を
加熱溶融し、これに必要に応じた色素、香料、薬
剤成分等の任意成分を加え均一となるまで混合
し、更に得られた混合物を型に流し込み、冷却、
固化させ、棒状に成型することにより製造され
る。
本発明で使用される油性基材としては、カルナ
ウバワツクス、キヤンデリラワツクス、ライスワ
ツクス、モウロウ、ミツロウ、セレシンワツク
ス、ミクロクリスタリンワツクス、パラフインワ
ツクス、硬化牛脂、硬化ヒマシ油、硬化ホホバ
油、ラノリン、ワセリン等の固体乃至準固体油性
基剤の他に流動パラフイン、スクワラン、オリー
ブ油、ヒマシ油、ホホバ油、シリコーン油、合成
エステル油等の液体油基剤が挙げられる。
また、任意成分としては何ら制約はないが、そ
の典型的なものとしては、酸化鉄、酸化チタン等
の無機顔料、レーキ顔料等の色素;酸化防止剤、
消炎剤、ビタミン剤、抗菌剤等の各種油性薬剤成
分;タルク、カオリン、金属石鹸、マイカパウダ
ー、セリサイト、ナイロンパウダー等が挙げられ
る。
斯くして得られた化粧料には、棒状で固化又は
半固体の化粧料のすべてが包含されるものであ
り、例えばステイツク状口紅、リツプクリーム、
ステイツク状アイシヤドウ、化粧ペンシル及びチ
ツク等が含まれる。
〔実施例〕
次に実施例を挙げて本発明を更に詳細に説明す
るが、本発明はこれらの実施例に制限されるもの
ではない。尚、例中の部は重量基準である。
実施例 1
(口紅)
第1表に示した各成分を80℃に加熱して均一に
混合し、成型用型に流し込み、冷却固化し口紅を
製造し、専門パネラー10名による性能評価を行つ
た。
結果を第2表に示す。
[Industrial Field of Application] The present invention relates to a solid cosmetic that is excellent in both feel of use and makeup durability. [Prior Art] Typical solid cosmetics include bar-shaped cosmetics such as lipsticks, lip balms, foundation sticks, and pencils; pencil-type cosmetics such as eyebrow pencils and eyeliner pencils;
There are pressed powders such as foundation, eye shadow, and blush, and oil-based cake-like cosmetics. Among these oil-based cosmetics, conventional oil-based cosmetics include carnauba wax, candelilla wax, ceresin, microcrystalline wax, hydrogenated animal and vegetable fats, solid fats such as beeswax, castor oil, olive oil, jojoba oil, squalane, various synthetic ester oils, etc. Powder is dispersed in a mixed system of liquid or semi-liquid oils such as silicone oil, liquid paraffin, and petrolatum. When attempting to manufacture solid cosmetics as described above by combining these conventionally used oils, it is possible to achieve the required performance of the product by adjusting the ratio of solid fat and liquid or semi-liquid oil. The feeling of use and makeup retention must be satisfied. However, it is difficult to satisfy these two requirements at the same time. The reason may be as follows. The organizational structure of oil-based cosmetics is generally thought to be one in which solid fat crystals form a network structure, and the network is filled with liquid oil.The strength and flexibility of this network structure is what makes cosmetics so effective. It plays a major role in the feeling of use and the longevity of makeup. That is, when there is a lot of solid fat (there is little liquid oil), the network structure becomes dense and the structure is strong, so the makeup lasts well, but it spreads hard and is hard to touch, giving a poor feeling of use. On the other hand, when there is less solid fat (more liquid oil), the mesh structure is coarser and the structure is weaker, making makeup less durable, but it spreads lightly, is soft to the touch, and has a good feel. In this way, it is difficult to simultaneously satisfy the performance requirements of cosmetics simply by adjusting the ratio of solid fat and liquid oil, and the same is true even by changing the type of oil. For example, in bar-shaped cosmetics such as lipsticks and pencil-type cosmetics such as eyeliners, reducing the amount of solid fat (increasing the amount of liquid oil) will result in products that spread easily, are soft to the touch, and have a good feel. When it comes to make-up lasting, it smears easily and discolors easily.
It is observed that the color transfers easily. On the other hand, if you increase the amount of solid fat (reduce the amount of liquid oil), you will experience a deterioration in the feel of the product, such as hard application, hard touch, and roughness, but your makeup will last longer. In addition, pressed powder type cosmetics have a large proportion of powder, and oil components such as those described above are used for the purpose of adjusting the feel during use and bonding or shape retention during molding. In this case, if the bonding force between the powder particles is insufficient, the powder may collapse during use, have low impact resistance, and may break or crack. On the other hand, if the bonding force between powder particles is too strong, it will be difficult to apply by puffing or brushing, and the appearance will deteriorate due to oily shine. It is difficult to solve this phenomenon by simply adjusting the ratio of solid fat and liquid oil, changing the type of oil, and adjusting molding conditions such as press pressure. [Problems to be solved by the present invention] As described above, when trying to manufacture solid cosmetics using only a combination of conventionally used oils, the necessary performance of the product, such as feel of use, long-lasting makeup, and It is difficult to simultaneously satisfy other desirable performances. The present invention aims to solve the drawbacks of the prior art and to provide a solid cosmetic that satisfies both the feeling of use and the makeup's longevity. [Means for solving the problem] The present inventors have previously determined that the number of carbon atoms in the molecule is
Mainly composed of mixed acid group triglyceride having at least one saturated linear acyl group having 20 to 26 carbon atoms and at least one unsaturated acyl group having 16 to 22 carbon atoms, and saturated linear fatty acids having 20 to 26 carbon atoms and carbon as constituent fatty acids. The present inventors discovered that an excellent solid cosmetic could be obtained by blending a plastic oil containing a specific proportion of 16 to 22 unsaturated fatty acids (Japanese Patent Application No. 60-50124). Plastic fat, i.e. 20 carbon atoms in the molecule
~26 saturated straight chain acyl groups and at least one unsaturated acyl group having 16 to 22 carbon atoms, each consisting mainly of mixed acid group triglycerides, and having a constituent fatty acid composition of 30~30 to 26 saturated straight chain fatty acids having 20 to 26 carbon atoms 70% by weight, preferably 40 to 65% by weight, and 20 to 60% by weight, preferably 25 to 50% by weight of unsaturated fatty acids having 16 to 22 carbon atoms, and the formula (1) (wherein R contains a total of 11 to 23 carbon atoms,
It is a saturated aliphatic hydrocarbon group having at least one alkyl substituent from the carboxyl bond position to the center of the main chain. ) It has been found that by blending the branched fatty acid cholesteryl ester represented by the following formula, an excellent solid cosmetic without the above-mentioned drawbacks can be obtained. According to the present invention, there is provided a solid cosmetic that satisfies both the feeling of use and the makeup's longevity. When the plastic oil and fat used in the present invention is blended into cosmetics, it is found that it spreads very easily when applied to the skin and is soft on the touch, resulting in a remarkable effect of improving the feeling of use. It was also found that although the makeup lingering properties were improved to some extent, the improvement effect was still weak and unsatisfactory. Furthermore, the use of branched fatty acid cholesteryl ester used in the present invention in cosmetics has already been described in JP-A-56-65809 and JP-A-59-1407. has been shown to improve familiarity. In addition, although it was recognized that makeup lingering was improved to some extent, the effect was found to be weak and unsatisfactory. However, when the present inventors blended a branched fatty acid cholesteryl ester with the above-mentioned plastic oil and fat into a solid cosmetic, they discovered a remarkable synergistic effect between the two. That is, it has been found that a solid cosmetic can be obtained that has dramatically improved feel on use and long-lasting makeup compared to when these components are individually blended. Although its mechanism of action is not yet clear, it is speculated as follows. That is, it is thought that a flexible crystal network structure is formed by adding the plastic fat and oil and the branched fatty acid cholesteryl ester together. Therefore, when applied, the network structure is flexible, so the tissue is broken down appropriately, and as a result, it spreads easily, is soft to the touch, and provides a good feeling of use. On the other hand, since it is a flexible tissue, a part of the structure remains unbroken after application, and since the microscopic tissue slices are flexible, they are considered to be easy to adhere to the skin surface and have good makeup retention. The above-mentioned plastic oil and fat contained in the solid cosmetic of the present invention is preferably mainly composed of a disaturated-unsaturated mixed acid group triglyceride having two saturated linear acyl groups in the molecule. At least one of the saturated linear acyl groups in this mixed acid triglyceride has 20 to 26 carbon atoms, the other saturated linear acyl groups have 16 to 26 carbon atoms, and the unsaturated acyl group has 16 to 26 carbon atoms. 16 to 22. Among these, those in which the two saturated linear acyl groups each have 20 to 26 carbon atoms are more preferred. The remaining components of the plastic fat and oil are triglycerides whose constituent fatty acids are saturated linear fatty acids with 8 or more carbon atoms and/or unsaturated fatty acids with 8 or more carbon atoms, and these fatty acids have 16 to 24 carbon atoms. It is preferable that At this time, constituent fatty acids with less than 8 carbon atoms not only have a bad odor but also may cause skin irritation if hydrolyzed. In addition, in the present invention, a saturated linear acyl group having 20 to 26 carbon atoms and a saturated linear acyl group having 16 carbon atoms in the molecule
〜22 Mixed acid group triglyceride having at least one unsaturated acyl group each means that it is the largest component in the triglyceride, and the above disaturated monounsaturated type mixed acid group triglyceride is usually found in plastic fats and oils. This means that the content is about 35% or more, preferably 45% or more. Examples of the unsaturated fatty acids having 16 to 22 carbon atoms constituting the plastic mixed acid group triglyceride include oleic acid, linoleic acid, linoleic acid, etc. The bonding position thereof may be either α-position or β-position, but a mixture thereof may be used. preferable. Further, although there are no restrictions on the position or number of unsaturated bonds in the unsaturated fatty acid, from the viewpoint of oxidative stability, the number of unsaturated bonds is preferably 1 to 2. Saturated linear fatty acids having 20 to 26 carbon atoms include arachidic acid, behenic acid, etc.
If the number of carbon atoms is outside the range of 20 to 26, flexibility will be somewhat lacking. Furthermore, when the number of carbon atoms is 18 or less, the crystallinity becomes clearly high and it becomes brittle, so that the above-mentioned performance cannot be exhibited when blended into solid cosmetics. The content of the plastic oil and fat in the solid cosmetic of the present invention varies depending on the dosage form of the cosmetic, but it can be contained in the range of 0.1 to 80% by weight, and is usually contained in the range of 0.2 to 50% by weight. is preferable. If the concentration is below this range, sufficient effect cannot be obtained, and if the concentration is higher than this range, the effect will reach saturation, which is not only economically disadvantageous, but also the physical properties of the plastic fats and oils themselves will be expressed in the cosmetic, making it difficult to spread. The feeling of use deteriorates, and the performance of the cosmetic is impaired. The method for producing the plastic fats and oils used in the present invention is not particularly limited, but can be obtained, for example, by the method described in JP-A-60-53598. That is, a saturated linear fatty acid having 8 or more carbon atoms containing a predetermined amount or more of a saturated linear fatty acid having 20 to 26 carbon atoms, and a 8-carbon fatty acid containing a predetermined amount or more of an unsaturated fatty acid having 16 to 22 carbon atoms. It can be produced by transesterification of triglycerides in which the above-mentioned unsaturated fatty acids are constituent fatty acids, or by esterification of these fatty acids with glycerin. In order to increase the purity of the mixed acid group triglyceride in the present invention, it is preferable to remove high melting point parts and low melting point parts from the obtained triglyceride mixture by solvent fractionation or the like. The branched fatty acid (RCOOH) used in the production of the branched fatty acid cholesteryl ester used in the present invention can be one having 12 to 24 carbon atoms (11 to 23 carbon atoms as R);
-20 (R represents carbon number 13-19) is preferable. A branched fatty acid is a saturated branched fatty acid having at least one alkyl substituent from the carboxyl group bonding position to the center of the main chain. Such saturated branched fatty acids can be easily obtained from petrochemical raw materials or oleochemical raw materials. An example of such a branched fatty acid obtained from petrochemical raw materials is a branched fatty acid having a side chain at the α position, which is represented by the following formula. (In the formula, R 1 and R 2 are each a linear or branched saturated aliphatic hydrocarbon group, and the sum of the number of carbon atoms in R 1 and R 2 is 12 to 18.) Preferred specific examples of saturated branched fatty acids include 5,7,7-trimethyl-2-
(1,2,3-trimethylbutyl)-octanoic acid,
Examples include 2-heptylundecanoic acid, 2-hexyldecanoic acid, 2-octyldodecanoic acid, and 2-pentylnonanoic acid. An example of a saturated branched fatty acid obtained from oleochemical raw materials is a fatty acid having a methyl branched chain represented by the following formula. (In the formula, the sum of m and n is 14, and the distribution is centered around m = n = 7.) Such a methyl branched chain fatty acid is, for example, a methyl branched chain fatty acid obtained as a by-product during the production of oleic acid dimer. It is a branched isostearic acid and is commercially available, for example, as its isoproester (eg, Emery, USA). The branched fatty acid cholesteryl ester contained in the solid cosmetic of the present invention is produced by a conventional method for producing esters from the above-mentioned branched fatty acid or its derivative and cholesterol. The content of the branched fatty acid cholesteryl ester in the solid cosmetic of the present invention varies depending on the dosage form of the cosmetic, but it can be contained in the range of 0.01 to 50% by weight, and usually in the range of 0.03 to 30% by weight. It is preferable to let A sufficient effect cannot be obtained at a low concentration below this range, and even if a high concentration above this range is blended, the effect has already reached saturation, which is disadvantageous from an economical point of view, and branched fatty acids The physical properties of cholesteryl ester itself are expressed, and problems such as noticeable stickiness are likely to occur. The method for producing the branched fatty acid cholesteryl ester in the present invention is described in JP-A-56-65900, but the method for producing the branched fatty acid cholesteryl ester used in the solid cosmetic of the present invention is limited to this. It is not something that will be done. The production of the solid cosmetic (bar-shaped cosmetic) of the present invention includes:
It is carried out according to a conventional method except that each of the above-mentioned components is included in the respective amounts in the cosmetic composition. That is, the above amount of plastic oil and fat and branched fatty acid cholesteryl ester and an oily base such as oil, fat, wax, wax, etc. are heated and melted, and optional ingredients such as pigments, fragrances, and drug ingredients are added to this mixture to make it uniform. Pour the resulting mixture into a mold, cool it,
Manufactured by solidifying and molding into a rod shape. The oil base materials used in the present invention include carnauba wax, candelilla wax, rice wax, mou wax, beeswax, ceresin wax, microcrystalline wax, paraffin wax, hydrogenated beef tallow, hydrogenated castor oil, and hydrogenated jojoba. In addition to solid or semi-solid oil bases such as oil, lanolin, and petrolatum, liquid oil bases such as liquid paraffin, squalane, olive oil, castor oil, jojoba oil, silicone oil, and synthetic ester oil may be mentioned. Although there are no restrictions on the optional components, typical examples include inorganic pigments such as iron oxide and titanium oxide, pigments such as lake pigments; antioxidants,
Various oil-based drug ingredients such as anti-inflammatory agents, vitamins, and antibacterial agents; examples include talc, kaolin, metal soap, mica powder, sericite, and nylon powder. The thus obtained cosmetics include all stick-shaped, solidified or semi-solid cosmetics, such as stick-shaped lipsticks, lip balms,
Includes stick-shaped eye shadows, cosmetic pencils, and ticks. [Examples] Next, the present invention will be explained in more detail with reference to Examples, but the present invention is not limited to these Examples. Note that parts in the examples are based on weight. Example 1 (Lipstick) Each component shown in Table 1 was heated to 80°C, mixed uniformly, poured into a mold, cooled and solidified to produce a lipstick, and its performance was evaluated by 10 expert panelists. . The results are shown in Table 2.
【表】【table】
【表】【table】
【表】【table】
【表】【table】
【表】
この結果から本発明品は、使用感(のび、つ
き、なめらかさ)、化粧もち(色落ち、にじみに
くさ)に於いて優れていることがわかる。
実施例 2
(アイブロウペンシル)
第3表に示した配合組成のアイブロウペンシル
を下記製法により製造し、専門パネラー10名によ
り性能評価を行つた。
結果を第4表に示す。[Table] From the results, it can be seen that the product of the present invention is excellent in the feeling of use (spreadability, stickiness, smoothness) and makeup retention (resistance to discoloration and smudging). Example 2 (Eyebrow Pencil) Eyebrow pencils having the formulation shown in Table 3 were manufactured by the following manufacturing method, and their performance was evaluated by 10 expert panelists. The results are shown in Table 4.
【表】
(製法)
各成分を80℃に加熱し、ロールミルで練合を繰
り返す。これを室温まで冷却し、圧搾射出機によ
つてノズルから芯を押し出して成型する。芯を、
芯型の溝を有する木部に装着し、接着、抱合、切
削にり、鉛筆型に成型し、製品とする。[Table] (Manufacturing method) Heat each ingredient to 80℃ and repeat kneading with a roll mill. This is cooled to room temperature and molded by extruding the core from a nozzle using a squeeze injection machine. The core,
It is attached to a piece of wood with a core-shaped groove, glued, conjugated, cut, and formed into a pencil shape to produce a product.
【表】
この結果から本発明品は、使用感(書きやす
さ、柔らかさ、なめらかさ)、化粧もち(化粧く
ずれしない)に於いて優れていることがわかる。
実施例 3
(固型パウダーアイシヤドウ)
第5表に示した組成の固型パウダーアイシヤド
ウを下記製法により製造し、耐衝撃性評価及び専
門パネラー10名により性能評価を行つた。
結果を第6表に示す。[Table] From the results, it can be seen that the product of the present invention is excellent in terms of usability (ease of writing, softness, smoothness) and makeup retention (makeup does not come off). Example 3 (Solid powder eye shadow) Solid powder eye shadow having the composition shown in Table 5 was manufactured by the following manufacturing method, and impact resistance evaluation and performance evaluation were performed by 10 expert panelists. The results are shown in Table 6.
【表】
(製法)
粉末部をブレンダーで撹拌混合し、これに加熱
均一溶解した油相部を吹きつけ、更に撹拌する。
その後粉枠して、成型機で圧縮成型し、固型パウ
ダーアイシヤドウを得る。[Table] (Manufacturing method) The powder part is stirred and mixed in a blender, and the heated and uniformly dissolved oil phase is sprayed onto this, and further stirred.
After that, it is formed into a powder frame and compression molded using a molding machine to obtain a solid powder eye shadow.
【表】【table】
【表】
この結果から本発明品は、使用感(伸ばしやす
さ、つき)、化粧もち(よれ、とれ)に於いて優
れていることがわかる。[Table] From the results, it can be seen that the product of the present invention is excellent in the feeling of use (ease of spreading, stickiness) and makeup retention (bending, removal).
Claims (1)
及び炭素数16〜22の不飽和アシル基をそれぞれ少
なくとも1つ有する混酸基トリグリセリドを主体
とし、かつ構成脂肪酸組成が炭素数20〜26の飽和
直鎖脂肪酸30〜70重量%、炭素数16〜22の不飽和
脂肪酸20〜60重量%である可塑性油脂と、式(1) (式中、Rは合計11〜23個の炭素原子を含有し、
カルボキシル結合位から主鎖の中心までに、少な
くとも1つのアルキル置換基を有する飽和脂肪族
炭化水素基である。) で表わされる分岐脂肪酸コレステリルエステルを
含有することを特徴とする固型化粧料。[Scope of Claims] 1. Mainly composed of mixed acid group triglyceride having at least one saturated linear acyl group having 20 to 26 carbon atoms and at least one unsaturated acyl group having 16 to 22 carbon atoms in the molecule, and constituent fatty acid composition is 30 to 70% by weight of a saturated straight chain fatty acid having 20 to 26 carbon atoms and 20 to 60% by weight of an unsaturated fatty acid having 16 to 22 carbon atoms, and the formula (1) (wherein R contains a total of 11 to 23 carbon atoms,
It is a saturated aliphatic hydrocarbon group having at least one alkyl substituent from the carboxyl bond position to the center of the main chain. ) A solid cosmetic containing a branched fatty acid cholesteryl ester represented by:
Priority Applications (7)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP19697485A JPS6256416A (en) | 1985-09-06 | 1985-09-06 | Solid cosmetic |
ES552946A ES8800125A1 (en) | 1985-03-13 | 1986-03-12 | Solid cosmetic preparation. |
EP86301827A EP0194887B1 (en) | 1985-03-13 | 1986-03-13 | Solid cosmetic preparation |
DE8686301827T DE3673669D1 (en) | 1985-03-13 | 1986-03-13 | SOLID COSMETIC PREPARATION. |
MYPI87000624A MY101733A (en) | 1985-03-13 | 1987-05-11 | Solid cosmetic preparation. |
US07/208,792 US5011680A (en) | 1985-03-13 | 1988-06-15 | Solid cosmetic preparation |
HK49/91A HK4991A (en) | 1985-03-13 | 1991-01-10 | Solid cosmetic preparation |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP19697485A JPS6256416A (en) | 1985-09-06 | 1985-09-06 | Solid cosmetic |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS6256416A JPS6256416A (en) | 1987-03-12 |
JPH0144165B2 true JPH0144165B2 (en) | 1989-09-26 |
Family
ID=16366736
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP19697485A Granted JPS6256416A (en) | 1985-03-13 | 1985-09-06 | Solid cosmetic |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS6256416A (en) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2003204753A (en) * | 2001-11-06 | 2003-07-22 | Kao Corp | Triglyceride composition |
-
1985
- 1985-09-06 JP JP19697485A patent/JPS6256416A/en active Granted
Also Published As
Publication number | Publication date |
---|---|
JPS6256416A (en) | 1987-03-12 |
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