JPH07304633A - Cosmetic blended with organic-inorganic composite pigment - Google Patents

Cosmetic blended with organic-inorganic composite pigment

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Publication number
JPH07304633A
JPH07304633A JP6120521A JP12052194A JPH07304633A JP H07304633 A JPH07304633 A JP H07304633A JP 6120521 A JP6120521 A JP 6120521A JP 12052194 A JP12052194 A JP 12052194A JP H07304633 A JPH07304633 A JP H07304633A
Authority
JP
Japan
Prior art keywords
red
pigment
white pigment
organic
inorganic
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
JP6120521A
Other languages
Japanese (ja)
Other versions
JP3241535B2 (en
Inventor
Masaaki Horino
政章 堀野
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.)
Pola Chemical Industries Inc
Original Assignee
Pola Chemical Industries Inc
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 Pola Chemical Industries Inc filed Critical Pola Chemical Industries Inc
Priority to JP12052194A priority Critical patent/JP3241535B2/en
Publication of JPH07304633A publication Critical patent/JPH07304633A/en
Application granted granted Critical
Publication of JP3241535B2 publication Critical patent/JP3241535B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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Abstract

PURPOSE:To obtain a cosmetic having excellent chroma and opacifying power and not causing bleeding to water and ethanol. CONSTITUTION:This cosmetic blended with organic-inorganic composite pigment obtained by coating inorganic white pigment having >=2 refractive index and 0.1-0.67mum average particle diameter with calcium carbonate and red No.102. Zinc oxide, zirconia oxide, anatase type or rutile type titanium oxide may be cited as the inorganic white pigment. The composite pigment is obtained by dissolving red No.201 and/or red No.202 in a lower alcohol, dispersing the inorganic white pigment into the solution, then adding an alkali carbonate or its solution to deposit red No.201 and/or red No.202 on the surface of the white pigment, adding a solution of a lower alcohol of calcium chloride to the alcohol solution to deposit calcium carbonate on the surface of the pigment and making or remaking red No.201 and/or red No.202 deposited on the surface of the pigment into a lake.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明は高彩度、高隠蔽性を持
ち、水や汗に対してブリーディングを生じにくい化粧料
に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a cosmetic having high saturation and high concealing property, which hardly causes bleeding with respect to water or sweat.

【0002】[0002]

【従来の技術】アイカラー、口紅等に用いられる有色顔
料としては、一般に無機顔料、有機顔料、パール顔料等
が汎用されている。このようなポイントメークアップ料
は、塗布した際の仕上がり感を良好なものとするため
に、色味の発色が均一であり、下地色(肌や口唇の色)
の影響を受けず、彩度が高い事、経時変化で色がくすん
だりしない事、着色力が充分にあり、塗布部位に染着し
ない事が重要である。
Inorganic pigments, organic pigments, pearl pigments and the like are generally used as colored pigments used in eye colors, lipsticks and the like. In order to improve the feeling of finish when applied, such a point make-up material has a uniform color tone and has a base color (skin and lip color).
It is important that it is not affected by the above, has a high saturation, does not have a dull color due to aging, has sufficient coloring power, and does not stain the application site.

【0003】しかし色調の面から述べると、赤色系無機
顔料であるベンガラ類はそのもの自身の彩度が低いとい
う問題を有している。更にベンガラ類は皮膚から分泌さ
れる皮脂や水分により濡れると、色調が赤黒く変化して
しまう。又黄色水和酸化鉄は皮膚から分泌される皮脂や
水分により濡れると、屈折率が低下してしまう。そのた
めにこのような有色無機顔料を使用したポイントメイク
アップ料は、経時で赤黒い色調に変化したり、光学的に
下地の肌色を反映するようになるため、塗布色がくすん
でくるという欠点を有していた。
However, from the viewpoint of color tone, red iron oxides such as red iron oxide have a problem that they have low saturation. Furthermore, red iron oxide changes its color to reddish black when it becomes wet with sebum and water secreted from the skin. Further, the yellow hydrated iron oxide has a reduced refractive index when it is wet with sebum or water secreted from the skin. Therefore, point makeup products that use such colored inorganic pigments have the drawback that the coating color becomes dull because it changes to a reddish black color tone over time and it optically reflects the skin color of the base. Was.

【0004】一方有機顔料としては、建染染料である赤
色226号、赤色202号、黄色4号アルミニウムレー
キ、黄色5号アルミニウムレーキ、青色1号アルミニウ
ムレーキ等が汎用されている。しかし、赤色226号以
外の染料はブリーディングを起こして塗布部位に染着す
るという問題を有しているが、有機顔料の業界において
はこれら染料の化学構造から見て溶出、染着現象は避け
られないものとされ、有効な対策は未だ見いだされてい
ない。そのため、化粧料、特に多量に配合される事が多
いアイカラーや口紅の着色剤として使用した場合、塗布
部位への染着性を抑える事が課題として残っている。
On the other hand, as organic pigments, vat dyes such as red No. 226, red No. 202, yellow No. 4 aluminum lake, yellow No. 5 aluminum lake, and blue No. 1 aluminum lake are generally used. However, dyes other than Red No. 226 have a problem of causing bleeding and dyeing at the coating site, but in the organic pigment industry, the elution and dyeing phenomena are unavoidable in view of the chemical structure of these dyes. No effective measures have been found yet. Therefore, when used as a colorant for cosmetics, especially eye colors and lipsticks that are often mixed in large amounts, it remains a problem to suppress the dyeing property to the application site.

【0005】又、口紅に有機顔料を配合する場合、彩度
を高める方法として顔料の分散粒子を小さくする事が知
られており、このために従来より有機顔料と油剤とを3
本ロール等の強力な混合装置を使用してよく練り合わせ
る技術が行われているが、この技術によっても分散させ
た有機顔料が再凝集してしまったり、或いは分散させた
有機顔料粒子間の距離が非常に接近している為、光学的
に充分な分散状態を得られない現象は避けられず、有機
顔料の高彩度化が充分に為されているとは言い難い。
In addition, when an organic pigment is blended with lipstick, it is known to reduce the dispersed particles of the pigment as a method of increasing the saturation.
A technique of kneading well using a powerful mixing device such as this roll has been performed, but this technique also causes the dispersed organic pigment to re-aggregate, or the distance between dispersed organic pigment particles. Since they are very close to each other, it is unavoidable that a sufficiently dispersed state cannot be obtained optically, and it cannot be said that the saturation of the organic pigment is sufficiently high.

【0006】美爪料においては、美爪料に用いられる有
機顔料やパール顔料と二酸化チタンとでは比重差が大き
いため、色分かれやケーキングの原因となり、中には再
分散不可能な場合も生じるため、著しく商品価値を損な
うものであった。
[0006] In the nail enamel, since there is a large difference in specific gravity between the organic pigment or pearl pigment used in the nail enamel and titanium dioxide, it causes color separation or caking, and in some cases, redispersion is impossible. Therefore, the product value was significantly impaired.

【0007】このような従来技術の欠点を改良した技術
としては、一般の無機顔料又は有機顔料と雲母チタン等
の光沢顔料との複合化が行われている。係る方法として
は例えば (1)光沢顔料の表面に固有の色を有する酸化鉄、酸化
ニッケル、酸化コバルト、酸化銅、酸化クロム等を被覆
する方法(特公昭63−25644号公報)。 (2)光沢顔料表面に水酸化アルミニウム層を固着さ
せ、次いでキレート形成剤、難溶性塩形成基を有する染
料を利用し、顔料表面に染料を固定化させる方法(特開
昭51−17910号公報)。 (3)光沢顔料表面に赤色202号を種々の方法で固着
させる方法(特開昭62−169716号公報)。 (4)光沢顔料表面を酸性染料と塩基性アルミニウム塩
との不溶性塩で被覆する方法(特開平2−34669号
公報)。 (5)プラスチック粉体に顔料を複合化させる事によ
り、分散媒に対する分散性を向上させる方法(特開昭5
8−187459号公報) (6)ナイロン球やポリエチレン球、球状シリカに赤色
202号を混合し、回転式ボールミルによりそれらを複
合化させる方法(特開平4−292664号公報)。 (7)表面電荷が同じ真珠光沢顔料と着色料とを表面電
荷調整剤を用い付着させ、外観色が鮮明で適度な光沢感
を有する複合光沢顔料を得る方法(特開平4−3327
66号公報)。 等が提案されている。
As a technique for improving the drawbacks of the prior art, a general inorganic pigment or organic pigment and a lustrous pigment such as mica titanium are compounded. Examples of such methods include (1) a method of coating the surface of a luster pigment with iron oxide, nickel oxide, cobalt oxide, copper oxide, chromium oxide or the like having a unique color (Japanese Patent Publication No. 63-25644). (2) A method of fixing an aluminum hydroxide layer on the surface of a luster pigment and then fixing the dye on the surface of the pigment by using a chelate-forming agent and a dye having a sparingly soluble salt-forming group (JP-A-51-17910). ). (3) A method of fixing Red No. 202 on the surface of the luster pigment by various methods (Japanese Patent Laid-Open No. 62-169716). (4) A method of coating the surface of the luster pigment with an insoluble salt of an acidic dye and a basic aluminum salt (JP-A-2-34669). (5) A method of improving the dispersibility in a dispersion medium by compounding a pigment with a plastic powder (Japanese Patent Laid-Open No. Sho 5)
(No. 8-187459) (6) A method of mixing Nylon spheres, polyethylene spheres, and spherical silica with Red No. 202 and compounding them by a rotary ball mill (JP-A-4-292664). (7) A method in which a pearlescent pigment having the same surface charge and a colorant are adhered to each other by using a surface charge adjusting agent to obtain a complex gloss pigment having a clear appearance color and an appropriate gloss feeling (JP-A-4-3327).
No. 66). Etc. have been proposed.

【0008】[0008]

【発明が解決しようとする課題】しかしながら、(1)
〜(4)、(6)、(7)の技術では、着色力が不充分
であり、透明感はあるものの、顔料の発色性に問題を残
している。更に(2)〜(6)の技術では有機顔料がブ
リーディングを起こして、塗布部位に染着し易い欠点が
ある。
[Problems to be Solved by the Invention] However, (1)
In the techniques (4), (6), and (7), the coloring power is insufficient and a transparent feeling is obtained, but the coloring property of the pigment remains a problem. Furthermore, the techniques (2) to (6) have a drawback that the organic pigment causes bleeding and is likely to be dyed at the application site.

【0009】そこで本発明は前記従来技術の問題点を解
決し、高彩度、高隠蔽性を持ち、ブリーディングを生じ
にくい、分散性、色調の経時安定性に優れた化粧料を提
供する事を課題とする。
Therefore, the present invention solves the above-mentioned problems of the prior art, and provides a cosmetic having high saturation and high hiding property, hardly causing bleeding, dispersibility and stability of color tone over time. To do.

【0010】[0010]

【課題を解決するための手段】本発明者らは上記課題を
解決するため、鋭意研究を重ねた結果、高屈折率無機白
色顔料表面に炭酸カルシウムと赤色202号とを均一且
つ強固に付着させて複合化した顔料を化粧料に配合した
場合には単に高屈折率無機白色顔料と赤色202号とを
配合した場合よりもはるかに高彩度、高隠蔽力を示し、
また水や汗、エタノールに対してブリーディングを生じ
にくい事、更に処方中での分散性、色調の経時安定性に
も優れている事を見いだし、本発明を完成させるに至っ
た。
The inventors of the present invention have conducted extensive studies in order to solve the above-mentioned problems, and as a result, have made calcium carbonate and red No. 202 adhere uniformly and firmly to the surface of a high-refractive-index inorganic white pigment. When the compounded pigment is compounded into a cosmetic, it exhibits much higher chroma and high hiding power than when simply compounded with a high refractive index inorganic white pigment and Red No. 202.
Further, they have found that bleeding is unlikely to occur in water, sweat and ethanol, and that they are excellent in dispersibility in the formulation and stability of color tone over time, and have completed the present invention.

【0011】即ち本発明は、高彩度、高隠蔽性を持ち、
赤色202号の塗布部位への染着が無く、色調の経時安
定性に優れた化粧料を提供する。
That is, the present invention has high saturation and high concealability,
(EN) Provided is a cosmetic which does not stain Red 202 and has excellent color stability over time.

【0012】以下に本発明を詳細に説明する。The present invention will be described in detail below.

【0013】本発明に適用される、無機白色顔料を炭酸
カルシウムと赤色202号とで強固に被覆してなる有機
−無機複合顔料は、(1)赤色201号及び/又は赤色
202号を低級アルコールに溶解する工程と(2)赤色
201号及び/又は赤色202号を溶解した低級アルコ
ール溶液に無機白色顔料を分散させる工程と(3)該低
級アルコール溶液にアルカリ剤を添加して、無機白色顔
料表面に赤色201号及び/又は赤色202号を沈着さ
せる工程と(4)該低級アルコール溶液に、塩化カルシ
ウムの低級アルコール溶液を添加して炭酸カルシウムを
無機白色顔料表面に生成、沈着させるとともに、無機白
色顔料表面に沈着させた赤色201号及び/又は赤色2
02号をレーキ化若しくは再レーキ化させ、無機白色顔
料の表面に炭酸カルシウムと赤色202号とを固着させ
る工程とから製造される。
The organic-inorganic composite pigment which is applied to the present invention and which is obtained by firmly coating the inorganic white pigment with calcium carbonate and Red No. 202 is (1) Red No. 201 and / or Red No. 202 as a lower alcohol. And (2) a step of dispersing an inorganic white pigment in a lower alcohol solution in which Red No. 201 and / or Red No. 202 is dissolved, and (3) an inorganic white pigment by adding an alkali agent to the lower alcohol solution. A step of depositing Red No. 201 and / or Red No. 202 on the surface, and (4) adding a lower alcohol solution of calcium chloride to the lower alcohol solution to generate and deposit calcium carbonate on the surface of the inorganic white pigment, Red No. 201 and / or Red No. 2 deposited on the surface of the white pigment
No. 02 is laked or re-laked, and calcium carbonate and red No. 202 are fixed to the surface of the inorganic white pigment.

【0014】(1)と(2)の工程は前後しても、或い
は同時に行っても差し支えないが、赤色201号及び/
又は赤色202号の溶解状態や、無機白色顔料の分散状
態を確認するためには、上記手順に従う方が好ましい。
The steps (1) and (2) may be carried out before or after, or at the same time.
Alternatively, in order to confirm the dissolved state of Red No. 202 and the dispersed state of the inorganic white pigment, it is preferable to follow the above procedure.

【0015】赤色201号及び/又は赤色202号を溶
解させ、無機白色顔料を分散させる低級アルコールとし
てはメタノール、エタノール、イソプロピルアルコー
ル、n−プロピルアルコール、イソブタノール、sec
−ブタノール、tert−ブタノール、n−ブタノール
等を一種又は二種以上を混合して用いる事が出来る。
Lower alcohols for dissolving Red No. 201 and / or Red No. 202 and dispersing the inorganic white pigment are methanol, ethanol, isopropyl alcohol, n-propyl alcohol, isobutanol, sec.
-Butanol, tert-butanol, n-butanol and the like can be used alone or in combination of two or more.

【0016】これらの低級アルコールは、含水量が多い
と(3)の工程においてアルカリ剤を添加した際に、無
機白色顔料が強く凝集してしまい、不均一な被覆状態の
有機−無機複合顔料となる事があるので、含水量が5%
未満の低級アルコールを用いる事が望ましい。
When the lower alcohol has a high water content, the inorganic white pigment is strongly aggregated when the alkaline agent is added in the step (3), resulting in an organic-inorganic composite pigment in a non-uniform coating state. The water content is 5%
It is desirable to use less than lower alcohols.

【0017】次に赤色201号及び/又は赤色202号
を溶解させ、無機白色顔料を分散させた低級アルコール
溶液に炭酸アルカリ塩若しくはその溶液をを添加し、赤
色201号及び/又は赤色202号を無機白色顔料の表
面に沈着させる。炭酸アルカリ塩としてはNa2 CO
3 、K2 CO3 、Li2 CO3 の一種又は二種以上をそ
のまま、或いは水溶液、低級アルコール溶液、含水低級
アルコール溶液として好適に使用でき、その濃度は特に
限定されないが、赤色201号及び/又は赤色202号
を無機白色顔料表面に沈着せしめるだけの量を導入する
必要があるので、作業上の効率から見れば、極力高濃度
の溶液として使用する事が望ましい。
Next, red No. 201 and / or red No. 202 is dissolved, and an alkali carbonate or a solution thereof is added to a lower alcohol solution in which an inorganic white pigment is dispersed, and red No. 201 and / or red No. 202 is added. Deposit on the surface of the inorganic white pigment. Na 2 CO as the carbonate carbonate
One or two or more of 3 , K 2 CO 3 and Li 2 CO 3 can be suitably used as they are or as an aqueous solution, a lower alcohol solution or a hydrous lower alcohol solution, and the concentration thereof is not particularly limited, but the red No. 201 and / or Alternatively, since it is necessary to introduce an amount sufficient to deposit Red No. 202 on the surface of the inorganic white pigment, it is desirable to use it as a solution having a concentration as high as possible from the viewpoint of work efficiency.

【0018】次いで(4)の工程では、炭酸カルシウム
を無機白色顔料表面に生成、沈着させるとともに、無機
白色顔料の表面に沈着させた赤色201号及び/又は赤
色202号を塩化カルシウムによりレーキ化若しくは再
レーキ化し、赤色202号の形態で強固に固着させる。
塩化カルシウムとしては無水塩、二水塩、六水塩の何れ
の形態でも好適に使用できる。塩化カルシウムを溶解さ
せる溶媒としてはメタノール、エタノール、イソプロパ
ノール等の低級アルコールが使用できるが、含水量が
0.5%未満の低級アルコールを使用した方が塩化カル
シウムの溶解速度が速いので好ましい。使用する濃度と
しては、特に限定されるものではないが、作業効率の点
からは極力高濃度の溶液を使用した方が有利である。
Then, in the step (4), calcium carbonate is generated and deposited on the surface of the inorganic white pigment, and the red No. 201 and / or the red No. 202 deposited on the surface of the inorganic white pigment are laked with calcium chloride or Re-lake and firmly fix in the form of Red No. 202.
As calcium chloride, any form of anhydrous salt, dihydrate and hexahydrate can be preferably used. As a solvent for dissolving calcium chloride, lower alcohols such as methanol, ethanol and isopropanol can be used, but lower alcohols having a water content of less than 0.5% are preferable because the dissolution rate of calcium chloride is faster. Although the concentration to be used is not particularly limited, it is advantageous to use a solution having a concentration as high as possible from the viewpoint of work efficiency.

【0019】塩化カルシウムにより、炭酸カルシウムを
無機白色顔料表面に生成、沈着させるとともに、無機白
色顔料の表面に沈着させた赤色201号及び/又は赤色
202号をレーキ化若しくは再レーキ化した後は使用し
た溶媒の沸点以下、好ましくは室温付近で反応の熟成を
行う事が好ましい。反応熟成時間は熟成温度により多少
の変動はあるが、3時間未満だと赤色202号本来の色
味である青みのある赤色の発色が得られない事があり、
又5時間以上熟成しても実質上色味の変化が認められな
いので、3〜5時間の熟成を行う事が望ましい。
Calcium carbonate is produced and deposited on the surface of the inorganic white pigment with calcium chloride, and red No. 201 and / or red No. 202 deposited on the surface of the inorganic white pigment are laked or relaked before use. The reaction is preferably aged at a temperature not higher than the boiling point of the solvent, preferably around room temperature. The reaction aging time may vary depending on the aging temperature, but if it is less than 3 hours, the bluish red color which is the original color of Red No. 202 may not be obtained,
Even if the aging is carried out for 5 hours or more, there is substantially no change in color tone, so it is desirable to carry out the aging for 3 to 5 hours.

【0020】反応熟成終了後、得られた有機−無機複合
顔料の濾過、洗浄を行う。有機−無機複合顔料を濾過す
る方法としては、加圧濾過、減圧濾過、自然濾過、遠心
分離、デカンテーション等の公知の方法を使用する事が
出来る。得られた有機−無機複合顔料の洗浄に使用する
溶媒としては、水、低級アルコール、或いはこれらの二
種以上の混合物を使用する事が出来る。
After completion of the reaction aging, the obtained organic-inorganic composite pigment is filtered and washed. As a method for filtering the organic-inorganic composite pigment, known methods such as pressure filtration, vacuum filtration, natural filtration, centrifugation, decantation and the like can be used. As a solvent used for washing the obtained organic-inorganic composite pigment, water, lower alcohol, or a mixture of two or more kinds of these can be used.

【0021】最終的に得られた無機白色顔料表面を炭酸
カルシウムと赤色202号とで被覆してなる有機−無機
複合顔料を乾燥する際には、60℃以下の温度で乾燥さ
せる事が望ましい。60℃を越える温度で乾燥させる
と、赤色202号の本来の色味より更に青みにずれる色
転位現象を生じ易い。乾燥時間は洗浄に使用した溶媒に
もよるが、通常は4〜30時間程度で充分である。
When drying the organic-inorganic composite pigment obtained by coating the surface of the finally obtained inorganic white pigment with calcium carbonate and Red No. 202, it is desirable to dry at a temperature of 60 ° C. or lower. When it is dried at a temperature over 60 ° C., a color shift phenomenon in which the color tint of Red No. 202 shifts to a bluish color is more likely to occur. The drying time depends on the solvent used for washing, but usually 4 to 30 hours is sufficient.

【0022】被覆される無機白色顔料は屈折率が2以上
のものが好ましい。屈折率が2未満のものを用いると透
明性が強くなり、下地の形態が見え易く且つ下地のアン
ダートーンの色味の影響を受けるため、高彩度、高隠蔽
力の顔料が得られない。このような屈折率が2以上の無
機白色顔料としては、酸化亜鉛(屈折率2.0)、酸化
ジルコニウム(屈折率2.4)、アナタース型酸化チタ
ン(屈折率2.5)、ルチル型酸化チタン(屈折率2.
75)やこれらの二種以上の混合物、複合物等が好適に
使用できる。
The inorganic white pigment to be coated preferably has a refractive index of 2 or more. When a material having a refractive index of less than 2 is used, the transparency becomes strong, the form of the base is easily visible, and the color tone of the undertone of the base is affected, so that a pigment with high saturation and high hiding power cannot be obtained. Such inorganic white pigments having a refractive index of 2 or more include zinc oxide (refractive index 2.0), zirconium oxide (refractive index 2.4), anatase type titanium oxide (refractive index 2.5), rutile type oxidation. Titanium (refractive index 2.
75) or a mixture or a mixture of two or more kinds of these can be preferably used.

【0023】無機白色顔料の形状については特に制限は
無いが、平均粒子径は0.1〜60μmの範囲にある事
が望ましい。平均粒子径が0.1μm未満であると、顔
料の隠蔽力が低下する上、光学的に充分な顔料分散状態
が得られにくく、60μmを越えると充分な着色力が得
られないだけでなく、粒子感が感じられるようになり、
化粧料として好ましくない。
The shape of the inorganic white pigment is not particularly limited, but the average particle diameter is preferably in the range of 0.1 to 60 μm. If the average particle size is less than 0.1 μm, the hiding power of the pigment is lowered, and it is difficult to obtain an optically sufficient pigment dispersion state. If the average particle size exceeds 60 μm, not only is sufficient coloring power not obtained. You can feel the graininess,
Not desirable as a cosmetic.

【0024】無機白色顔料に被覆する赤色202号の量
は、希望する色味に応じて選択する事が出来、無機白色
顔料表面に固着される赤色202号の量を多くすれば赤
色の濃い有機−無機複合顔料が得られるが、無機白色顔
料と赤色202号の比率が重量比で1対1を越えると実
質的に赤色が濃くならないので、この範囲内で適宜選択
する事が望ましい。
The amount of Red No. 202 coated on the inorganic white pigment can be selected according to the desired tint. If the amount of Red No. 202 adhered to the surface of the inorganic white pigment is increased, the reddish organic color will be deep. -Inorganic composite pigment can be obtained. However, if the weight ratio of the inorganic white pigment to Red No. 202 exceeds 1: 1, the red color does not substantially darken. Therefore, it is preferable to appropriately select within this range.

【0025】以下、本発明に適用される有機−無機複合
顔料を製造例により更に詳細に説明する。
Hereinafter, the organic-inorganic composite pigment applied to the present invention will be described in more detail with reference to production examples.

【0026】製造例1.ガラス容器に95%エタノール
200gを秤量し、赤色202号(大東化成製)2gを
攪拌しながら投入し、完全に溶解させた。この溶液に酸
化チタンA−100(石原産業製)8gを投入し、ホモ
ミキサーを用いて30分攪拌を続けて均一分散させた。
別途精製水40gに炭酸ナトリウム13.4gを溶解さ
せたアルカリ溶液を用意し、酸化チタンを分散させた赤
色202号のエタノール溶液に30分かけてゆっくり注
入した。更に99.5%エタノール100gに無水塩化
カルシウム80gを溶解させた液を、60分かけて添加
した。その後室温で4時間反応熟成をした。熟成完了
後、デカンテーションにより上澄み液を除去し、精製水
300gを加え、攪拌、濾過する工程を3回、95%エ
タノール200gを加え、攪拌、濾過する工程を3回繰
り返した。得られた有機−無機複合顔料を50℃で12
時間乾燥し、粉砕して、酸化チタン表面に炭酸カルシウ
ムと赤色202号とが強固に固着した有機−無機複合顔
料を得た。
Production Example 1. 200 g of 95% ethanol was weighed into a glass container, and 2 g of Red No. 202 (manufactured by Daito Kasei) was added with stirring to completely dissolve it. 8 g of titanium oxide A-100 (manufactured by Ishihara Sangyo Co., Ltd.) was added to this solution, and stirring was continued for 30 minutes using a homomixer to uniformly disperse the mixture.
Separately, an alkaline solution in which 13.4 g of sodium carbonate was dissolved in 40 g of purified water was prepared, and slowly poured into an ethanol solution of Red No. 202 in which titanium oxide was dispersed, over 30 minutes. Further, a solution prepared by dissolving 80 g of anhydrous calcium chloride in 100 g of 99.5% ethanol was added over 60 minutes. Then, the reaction was aged at room temperature for 4 hours. After completion of the aging, the supernatant was removed by decantation, and the steps of adding 300 g of purified water, stirring and filtering were repeated 3 times, and 200 g of 95% ethanol was added, and the steps of stirring and filtering were repeated 3 times. The obtained organic-inorganic composite pigment was added at
It was dried for an hour and pulverized to obtain an organic-inorganic composite pigment in which calcium carbonate and Red No. 202 were firmly fixed on the surface of titanium oxide.

【0027】製造例2.ガラス容器に95%エタノール
200gを秤量し、赤色202号(大東化成製)2gと
赤色201号(癸巳化成製)1gとを攪拌しながら投入
し、完全に溶解させた。この溶液に酸化チタンCR−5
0(石原産業製)7.5gと酸化ジルコニウム(東ソー
製)2gとを投入し、ディスパーを用いて8000rp
mで30分攪拌を続けて均一分散させた。別途精製水8
0gに炭酸ナトリウム13.4gを溶解させたアルカリ
溶液を用意し、酸化チタンと酸化ジルコニウムとを分散
させた赤色202号と赤色201号とのエタノール溶液
に30分かけてゆっくり注入した。更に95%エタノー
ル100gに塩化カルシウム・六水塩を溶解させた溶液
を60分かけて添加した。その後室温で5時間反応熟成
をした。熟成完了後、デカンテーションにより上澄み液
を除去し、精製水300gを加え、攪拌、濾過する工程
を3回、95%エタノール200gを加え、攪拌、濾過
する工程を3回繰り返した。得られた有機−無機複合顔
料を50℃で10時間乾燥し、粉砕して、酸化チタン及
び酸化ジルコニウム表面に炭酸カルシウムと赤色202
号とが強固に固着した有機−無機複合顔料を得た。
Production Example 2. In a glass container, 200 g of 95% ethanol was weighed, and 2 g of Red No. 202 (manufactured by Daito Kasei) and 1 g of Red No. 201 (manufactured by Konami Kasei) were charged with stirring to completely dissolve them. Titanium oxide CR-5 was added to this solution.
0 g (made by Ishihara Sangyo) and 7.5 g of zirconium oxide (made by Tosoh) were charged, and 8000 rp using a disper.
At m, stirring was continued for 30 minutes to uniformly disperse. Separately purified water 8
An alkaline solution prepared by dissolving 13.4 g of sodium carbonate in 0 g was prepared, and slowly poured into an ethanol solution of red No. 202 and red No. 201 in which titanium oxide and zirconium oxide were dispersed, over 30 minutes. Furthermore, a solution prepared by dissolving calcium chloride / hexahydrate in 100 g of 95% ethanol was added over 60 minutes. Then, the reaction was aged at room temperature for 5 hours. After completion of the aging, the supernatant was removed by decantation, and the steps of adding 300 g of purified water, stirring and filtering were repeated 3 times, and 200 g of 95% ethanol was added, and the steps of stirring and filtering were repeated 3 times. The obtained organic-inorganic composite pigment is dried at 50 ° C. for 10 hours and pulverized to give calcium carbonate and red 202 on the surfaces of titanium oxide and zirconium oxide.
To obtain an organic-inorganic composite pigment in which No. 1 and No. 3 are firmly fixed.

【0028】製造例3.ガラス容器に95%エタノール
200gを秤量し、赤色202号(癸巳化成製)0.5
gを攪拌しながら投入し、完全に溶解させた。この溶液
に酸化チタンA−100(石原産業製)9gと酸化亜鉛
(堺化学製)1gとを投入し、ディスパーを用いて90
00rpmで30分攪拌を続けて均一分散させた。別途
精製水40gに炭酸ナトリウム13.4gを溶解させた
アルカリ溶液を用意し、酸化チタンと酸化亜鉛とを分散
させた赤色202号と赤色201号とのエタノール溶液
に30分かけてゆっくり注入した。更に95%エタノー
ル100gに無水塩化カルシウム80gを溶解させた溶
液を60分かけて添加した。その後室温で4時間反応熟
成をした。熟成完了後、デカンテーションにより上澄み
液を除去し、精製水300gを加え、攪拌、濾過する工
程を3回、95%エタノール200gを加え、攪拌、濾
過する工程を3回繰り返した。得られた有機−無機複合
顔料を30℃で24時間乾燥し、粉砕して酸化チタン及
び酸化亜鉛表面に炭酸カルシウムと赤色202号とが強
固に固着した有機−無機複合顔料を得た。
Production Example 3. 200 g of 95% ethanol was weighed in a glass container, and red No. 202 (manufactured by Konami Kasei) 0.5
g was added with stirring to completely dissolve it. To this solution, 9 g of titanium oxide A-100 (manufactured by Ishihara Sangyo) and 1 g of zinc oxide (manufactured by Sakai Chemical Co., Ltd.) were charged, and 90 using a disper.
Stirring was continued at 00 rpm for 30 minutes to uniformly disperse. Separately, an alkaline solution prepared by dissolving 13.4 g of sodium carbonate in 40 g of purified water was prepared, and slowly poured into an ethanol solution of red No. 202 and red No. 201 in which titanium oxide and zinc oxide were dispersed, over 30 minutes. Further, a solution prepared by dissolving 80 g of anhydrous calcium chloride in 100 g of 95% ethanol was added over 60 minutes. Then, the reaction was aged at room temperature for 4 hours. After completion of the aging, the supernatant was removed by decantation, and the steps of adding 300 g of purified water, stirring and filtering were repeated 3 times, and 200 g of 95% ethanol was added, and the steps of stirring and filtering were repeated 3 times. The obtained organic-inorganic composite pigment was dried at 30 ° C. for 24 hours and pulverized to obtain an organic-inorganic composite pigment in which calcium carbonate and Red No. 202 were firmly adhered to the surfaces of titanium oxide and zinc oxide.

【0029】本発明に使用される有機−無機複合顔料
は、剤形や要求される外観色により異なるが、通常化粧
料中に0.01〜10重量%、好ましくは0.1〜5重
量%配合される。
The organic-inorganic composite pigment used in the present invention is usually 0.01 to 10% by weight, preferably 0.1 to 5% by weight in cosmetics, although it varies depending on the dosage form and the required appearance color. Be compounded.

【0030】又、本発明に使用される有機−無機複合顔
料は、彩度、隠蔽力に優れているため、赤色202号を
単に無機白色顔料と併用する場合よりも、配合される赤
色202号の量を実質的に低減する事が出来るので、皮
膚の安全面から見ても好ましいものである。
Since the organic-inorganic composite pigment used in the present invention is excellent in saturation and hiding power, Red 202 is blended more than when it is simply used in combination with an inorganic white pigment. The amount can be substantially reduced, which is preferable from the viewpoint of skin safety.

【0031】以下、実施例により本発明を更に詳細に説
明する。
Hereinafter, the present invention will be described in more detail with reference to Examples.

【0032】[0032]

【実施例】製造例1〜3の無機白色顔料を炭酸カルシウ
ムと赤色202号とで強固に被覆してなる有機−無機複
合顔料を使用して実施例1〜6の化粧料を製造した。
EXAMPLES Cosmetics of Examples 1 to 6 were produced using organic-inorganic composite pigments obtained by firmly coating the inorganic white pigments of Production Examples 1 to 3 with calcium carbonate and Red No. 202.

【0033】 実施例1.乳化型ファウンデーション (処方) 重量% 1.製造例1の複合顔料2.0%配合色素ペースト 21.0 2.ステアリン酸 1.75 3.非イオン界面活性剤 5.0 4.トリ−2-エチルヘキサン酸グリセリン 3.0 5.ブチルパラベン 0.1 6.PEG−400 1.0 7.カルボキシメチルセルロースナトリウム塩 0.1 8.メチルパラベン 0.2 9.トリエタノールアミン 0.7 10.珪酸アルミニウムマグネシウム 1.0 11.精製水 66.15 (製造法)1〜5の成分を85℃で溶解、分散させ、油
相組成物を得た。別途11の精製水に6〜10の成分を
溶解、混合し85℃まで加温して水相組成物を得た。油
相組成物に水相組成物を添加して乳化し、冷却して乳化
型ファウンデーションを得た。
Example 1. Emulsion type foundation (prescription) Weight% 1. Dye paste containing 2.0% of the composite pigment of Production Example 21.0 2. Stearic acid 1.75 3. Nonionic surfactant 5.0 4. Glycerin tri-2-ethylhexanoate 3.0 5. Butylparaben 0.1 6. PEG-400 1.0 7. Carboxymethyl cellulose sodium salt 0.1 8. Methylparaben 0.2 9. Triethanolamine 0.7 10. Aluminum magnesium silicate 1.0 11. Purified water 66.15 (Production method) Components 1 to 5 were dissolved and dispersed at 85 ° C to obtain an oil phase composition. Separately, 6 to 10 components were dissolved and mixed in 11 purified water and heated to 85 ° C. to obtain an aqueous phase composition. The aqueous phase composition was added to the oil phase composition to emulsify and then cooled to obtain an emulsified foundation.

【0034】 実施例2.頬紅 (処方) 重量% 1.タルク 66.75 2.セリサイト 13.0 3.カオリン 10.0 4.ミリスチン酸亜鉛 2.0 5.炭酸マグネシウム 1.0 6.製造例2の複合顔料 0.54 7.弁柄 1.1 8.ステアリン酸 2.5 9.流動パラフィン 2.2 10.ラノリン 0.6 11.非イオン界面活性剤 0.3 12.ビタミンE 0.01 (製造法)1〜7の成分を粉砕機で粉砕した後、ヘンシ
ェルミキサーに移し、60℃に温度を調整した。別途8
〜12の成分を85℃で溶解、混合させ、ヘンシェルミ
キサーに注入して、粉体部にコーティングし、冷却した
後取り出して粉砕機で粉砕し、プレス成型して頬紅を得
た。
Example 2. Blusher (prescription) wt% 1. Talc 66.75 2. Sericite 13.0 3. Kaolin 10.0 4. Zinc myristate 2.0 5. Magnesium carbonate 1.0 6. Composite pigment of manufacture example 0.54 7. Rouge 1.1 8. Stearic acid 2.5 9. Liquid paraffin 2.2 10. Lanolin 0.6 11. Nonionic surfactant 0.3 12. Vitamin E 0.01 (Production method) After crushing the components 1 to 7 with a crusher, they were transferred to a Henschel mixer and the temperature was adjusted to 60 ° C. 8 separately
The ingredients (12) were dissolved and mixed at 85 ° C., poured into a Henschel mixer, coated on the powder portion, cooled, taken out, crushed by a crusher, and press-molded to obtain a blusher.

【0035】 実施例3.リップカラー (処方) 重量% 1.イソステアリン酸ジグリセライド 14.7 2.トリ−2−エチルヘキサン酸グリセリン 6.8 3.グリセリン脂肪酸エステル 10.8 4.マイクロクリスタリンワックス 15.6 5.ビーズワックス 1.5 6.キャンデリラワックス 6.4 7.カルナバワックス 0.5 8.製造例3の複合顔料を2%含む色素ペースト 43.7 (製造法)1〜7の成分を90℃で混合溶解した後、8
の色素ペーストを添加、攪拌し均一に分散させて、減圧
して脱泡した。90℃に保持しながらリップ金型に充填
し、冷却してリップカラーを得た。
Example 3. Lip color (prescription) Weight% 1. Isostearic acid diglyceride 14.7 2. Glycerin tri-2-ethylhexanoate 6.8 3. Glycerin fatty acid ester 10.8 4. Microcrystalline wax 15.6 5. Bead wax 1.5 6. Candelilla wax 6.4 7. Carnauba wax 0.5 8. Dye Paste Containing 2% of Composite Pigment of Production Example 3 43.7 (Production Method) Components 1 to 7 were mixed and dissolved at 90 ° C., and then 8
The dye paste of (1) was added, and the mixture was stirred and uniformly dispersed. It was filled in a lip mold while maintaining at 90 ° C. and cooled to obtain a lip color.

【0036】 実施例4.アイカラー 重量% 1.製造例1の複合顔料 0.32 2.R−226−TiO2複合顔料 1.68 3.着色パール顔料 44.0 4.疎水化処理セリサイト 2.0 5.微粒子シリカ 2.0 6.ポリメチルシルセスキオキサン 4.0 7.タルク 34.0 8.スクワラン 2.0 9.液状ラノリン 2.0 10.非イオン界面活性剤 2.0 11.トリ−2−エチルヘキサン酸グリセリン 6.0 (製造法)1〜7の成分を粉砕機で粉砕した後、ヘンシ
ェルミキサーに移し、60℃に温度を調整した。別途8
〜12の成分を85℃で溶解、混合させ、ヘンシェルミ
キサーに注入して、粉体部にコーティングし、冷却した
後取り出して粉砕機で粉砕し、プレス成型してアイカラ
ーを得た。
Example 4. Eye color weight% 1. Composite pigment of Production Example 1 0.32 2. R-226-TiO2 composite pigment 1.68 3. Colored pearl pigment 44.0 4. Hydrophobized sericite 2.0 5. Fine particle silica 2.0 6. Polymethylsilsesquioxane 4.0 7. Talc 34.0 8. Squalane 2.0 9. Liquid lanolin 2.0 10. Nonionic surfactant 2.0 11. Glycerin tri-2-ethylhexanoate 6.0 (Production method) After crushing the components 1 to 7 with a crusher, they were transferred to a Henschel mixer and the temperature was adjusted to 60 ° C. 8 separately
The ingredients (12) to (12) were dissolved and mixed at 85 ° C., poured into a Henschel mixer, coated on the powder portion, cooled, taken out, pulverized by a pulverizer, and press-molded to obtain an eye color.

【0037】 実施例5.美爪料 (処方) 重量部 1.ニトロセルロース 15.0 2.アルキッド樹脂 12.0 3.フタル酸ジブチル 6.0 4.酢酸ブチル 23.0 5.酢酸エチル 9.0 6.エタノール 7.0 7.トルエン 25.0 8.製造例2の複合顔料 3.0 (製造法)1〜7の成分を混合溶解した後、これに8の
複合顔料を添加してボールミルで均一に分散させ、美爪
料を得た。
Example 5. Nails (prescription) parts by weight 1. Nitrocellulose 15.0 2. Alkyd resin 12.0 3. Dibutyl phthalate 6.0 4. Butyl acetate 23.0 5. Ethyl acetate 9.0 6. Ethanol 7.0 7. Toluene 25.0 8. Composite Pigment 3.0 of Production Example 2 (Production Method) The components of 1 to 7 were mixed and dissolved, and then the composite pigment of 8 was added and uniformly dispersed in a ball mill to obtain a nail enamel.

【0038】 実施例6.水性ネイルカラー (処方) 1.アクリルポリマーエマルション 78.7 2.カルビトール 7.7 3.フタル酸ジエチル 3.9 4.精製水 7.7 5.製造例3の複合顔料 1.4 6.ベントナイト 0.4 7.防腐剤 0.1 8.シリコーン系消泡剤 0.1 (製造法)精製水にカルビトールとフタル酸ジエチルを
加え、これに複合顔料を分散させた後、アクリルポリマ
ーエマルションと6〜8の成分を添加し均一になるよう
攪拌混合を行った。混合後、脱気処理を行い、水性ネイ
ルカラーを得た。
Example 6. Aqueous nail color (prescription) 1. Acrylic polymer emulsion 78.7 2. Carbitol 7.7 3. Diethyl phthalate 3.9 4. Purified water 7.7 5. Composite pigment of Production Example 1.4 6. Bentonite 0.4 7. Preservative 0.1 8. Silicone antifoaming agent 0.1 (Production method) Carbitol and diethyl phthalate are added to purified water, the composite pigment is dispersed therein, and then an acrylic polymer emulsion and 6 to 8 components are added to make the mixture uniform. Stir mixing was performed. After mixing, deaeration treatment was performed to obtain an aqueous nail color.

【0039】実施例1〜6に示した化粧料について光学
顕微鏡で観察した結果、いずれの化粧料もメジアン径で
およそ0.43〜0.47μmの範囲の均一な分散状態
を示しており、凝集体は認められなかった。
As a result of observing the cosmetics shown in Examples 1 to 6 with an optical microscope, all the cosmetics showed a uniform dispersion state in the range of 0.43 to 0.47 μm in median diameter. No collection was observed.

【0040】実施例1〜6の化粧料について、彩度と隠
蔽力を評価した。
The saturation and hiding power of the cosmetics of Examples 1 to 6 were evaluated.

【0041】(評価試料の調整方法)化粧料1.0gを
精秤し、ひまし油1.5gとともにフーバーマーラーを
用いて、150回混練した。混練したサンプル0.5g
を50ml容量のポリエチレン製ディスポーザブルカッ
プに秤取り、その中に透明ネイルエナメルラッカー10
gを入れ、均一になるまで攪拌した。攪拌中に揮発した
ネイルエナメルラッカーを補充して攪拌した後、隠蔽率
試験紙(日本テストパネル工業株式会社製)上に10m
ilのドクターブレードを用いて製膜して評価試料とし
た。
(Preparation Method of Evaluation Sample) 1.0 g of the cosmetic was precisely weighed and kneaded 150 times with 1.5 g of castor oil using a Hoover Mahler. Kneaded sample 0.5g
Weighed in a disposable disposable cup made of polyethylene with a capacity of 50 ml, and put 10 pieces of transparent nail enamel lacquer in it.
g, and stirred until uniform. After the nail enamel lacquer volatilized during stirring was replenished and stirred, 10 m was placed on a concealment rate test paper (manufactured by Japan Test Panel Industry Co., Ltd.).
A film was formed using an il doctor blade to give an evaluation sample.

【0042】(彩度の評価方法)隠蔽率試験紙に製膜し
た評価試料の白色部を、ミノルタ製分光色差計CM−1
000を用いて、分光スペクトルを測定し、L−a−b
値を算出した。
(Evaluation Method of Saturation) The white part of the evaluation sample formed on the concealment ratio test paper was replaced with a spectrophotometer CM-1 manufactured by Minolta.
000 is used to measure the spectrum and L-a-b
The value was calculated.

【0043】(隠蔽力の評価方法)隠蔽率試験紙の製膜
していない白色部と黒色部の400〜700nmにおけ
る分光スペクトルの差を100として、製膜した白色部
と黒色部の400〜700nmにおける分光スペクトル
の差を百分率に換算し隠蔽率を求めた。
(Evaluation Method of Concealment Power) Concealment Ratio The difference in the spectral spectrum between the white part and the black part of the test paper at 400 to 700 nm where the film is not formed is 100, and the white part and the black part where the film is formed are 400 to 700 nm. The concealment ratio was calculated by converting the difference in the spectral spectrum in 1 to the percentage.

【0044】以上の結果を表1にまとめて示す。The above results are summarized in Table 1.

【0045】[0045]

【表1】 [Table 1]

【0046】製造例1〜3の有機−無機複合顔料につい
て、以下の評価方法によりブリーディングの評価を実施
した。
The organic-inorganic composite pigments of Production Examples 1 to 3 were evaluated for bleeding by the following evaluation method.

【0047】1.水に対する溶出試験 精製水100g中に顔料6gを入れ、マグネチックスタ
ーラーで1時間攪拌した後、No.5cの濾紙で濾過
し、濾過液の505nmにおける光透過率を分光光度計
を用いて測定した。
1. Dissolution test in water After adding 6 g of pigment to 100 g of purified water and stirring with a magnetic stirrer for 1 hour, No. It filtered with the filter paper of 5c, and measured the light transmittance in 505 nm of the filtrate using a spectrophotometer.

【0048】2.95%エタノールに対する溶出試験 95%エタノール100g中に顔料1.5gを入れ、マ
グネチックスターラーで1時間攪拌した後、遠心分離機
を用いて3000rpmで30分間処理してから、テフ
ロン製濾過膜(MF−PTFE、0.5μm)で上澄み
液を濾過し、濾過液の505nmにおける光透過率を分
光光度計を用いて測定した。
2. Dissolution test for 95% ethanol 100 g of 95% ethanol was charged with 1.5 g of the pigment, stirred for 1 hour with a magnetic stirrer, treated with a centrifuge at 3000 rpm for 30 minutes, and then treated with Teflon. The supernatant was filtered through a filter membrane (MF-PTFE, 0.5 μm), and the light transmittance of the filtrate at 505 nm was measured using a spectrophotometer.

【0049】結果を表2に示す。The results are shown in Table 2.

【0050】[0050]

【表2】 [Table 2]

【0051】実施例1〜6の化粧料について、塗布後の
色調の変化と、塗布部位への染着性の有無を下記の方法
により評価した。
With respect to the cosmetics of Examples 1 to 6, the change in color tone after application and the presence or absence of dyeing property on the application site were evaluated by the following methods.

【0052】上腕内側部に2×2cmの大きさに実施例
1〜4の化粧料を塗布し、塗布直後及び塗布後3時間で
の色調の変化をミノルタ製分光測色計CM−2002で
調べた。更に6時間後にクレンジングクリーム及び水性
洗顔料を用いて、化粧料を除去し、塗布部位への有機顔
料の染着の有無を確認した。実施例5、6の化粧料は爪
に塗布し、同様に塗布直後及び塗布後3時間での色調の
変化をミノルタ製分光測色計CM−2002で調べた。
更に24時間後にリムーバーを用いて、美爪料を除去
し、爪への有機顔料の染着の有無を確認した。
The cosmetics of Examples 1 to 4 were applied to the inner side of the upper arm in a size of 2 × 2 cm, and the change in color tone immediately after application and 3 hours after application was examined with a spectrocolorimeter CM-2002 manufactured by Minolta. It was After 6 hours, the cleansing cream and the aqueous face wash were used to remove the cosmetics, and it was confirmed whether or not the organic pigment was dyed on the application site. The cosmetics of Examples 5 and 6 were applied to nails, and similarly, the change in color tone immediately after application and 3 hours after application was examined with a spectrocolorimeter CM-2002 manufactured by Minolta.
After 24 hours, the nail varnish was removed using a remover, and it was confirmed whether or not the organic pigment was dyed on the nail.

【0053】結果を表3に示す。The results are shown in Table 3.

【0054】[0054]

【表3】 [Table 3]

【0055】表1〜表3の結果に明らかなように、本発
明の化粧料は、彩度、隠蔽力に優れており、且つ塗布部
位への有機顔料の染着の恐れのないものであった。
As is clear from the results of Tables 1 to 3, the cosmetics of the present invention are excellent in saturation and hiding power, and there is no risk of dyeing the organic pigment on the application site. It was

【0056】[0056]

【発明の効果】本発明の化粧料により、彩度及び隠蔽力
に優れ、且つ塗布部位への有機顔料の染着の恐れがない
化粧料を得る事が出来る。
EFFECTS OF THE INVENTION With the cosmetic of the present invention, it is possible to obtain a cosmetic which is excellent in saturation and hiding power and is free from the risk of the organic pigment being dyed at the application site.

Claims (5)

【特許請求の範囲】[Claims] 【請求項1】 屈折率2以上且つ平均粒子径0.1〜6
0μmである無機白色顔料を炭酸カルシウムと赤色20
2号とで被覆した有機−無機複合顔料を配合する事を特
徴とする化粧料。
1. A refractive index of 2 or more and an average particle size of 0.1 to 6
Inorganic white pigment of 0 μm is added with calcium carbonate and red 20
A cosmetic comprising an organic-inorganic composite pigment coated with No. 2 as a blending agent.
【請求項2】 該有機−無機複合顔料が(1)赤色20
1号及び/又は赤色202号を低級アルコールに溶解す
る工程と(2)赤色201号及び/又は赤色202号を
溶解した低級アルコール溶液に無機白色顔料を分散させ
る工程と(3)該低級アルコール溶液に炭酸アルカリ塩
若しくはその溶液を添加して、無機白色顔料表面に赤色
201号及び/又は赤色202号を沈着させる工程と
(4)該低級アルコール溶液に、塩化カルシウムの低級
アルコール溶液を添加して炭酸カルシウムを無機白色顔
料表面に生成、沈着させるとともに、無機白色顔料表面
に沈着させた赤色201号及び/又は赤色202号をレ
ーキ化若しくは再レーキ化させ、無機白色顔料の表面に
炭酸カルシウムと赤色202号とを固着させる工程とを
特徴とする製造法により製造されたものである請求項1
に記載の化粧料。
2. The organic-inorganic composite pigment is (1) red 20.
No. 1 and / or Red No. 202 dissolved in a lower alcohol, (2) Dispersion of an inorganic white pigment in a lower alcohol solution in which Red No. 201 and / or Red No. 202 was dissolved, and (3) the lower alcohol solution. A step of depositing an alkali carbonate or a solution thereof to deposit Red No. 201 and / or Red No. 202 on the surface of the inorganic white pigment, and (4) adding a lower alcohol solution of calcium chloride to the lower alcohol solution. Calcium carbonate is generated and deposited on the surface of the inorganic white pigment, and red No. 201 and / or red No. 202 deposited on the surface of the inorganic white pigment is laked or re-laked to give calcium carbonate and red on the surface of the inorganic white pigment. No. 202 and a step of fixing the No. 202 to each other.
Cosmetics described in.
【請求項3】 該有機−無機複合顔料中の無機白色顔料
が酸化亜鉛、酸化ジルコニウム、酸化チタン(アナター
ス型)、酸化チタン(ルチル型)の一種又は二種以上の
組み合わせから選ばれる請求項1又は2の何れかに記載
の化粧料。
3. The inorganic white pigment in the organic-inorganic composite pigment is selected from zinc oxide, zirconium oxide, titanium oxide (anatase type) and titanium oxide (rutile type), or a combination of two or more thereof. Or the cosmetic according to any one of 2 above.
【請求項4】 該有機−無機複合顔料中の無機白色顔料
が酸化亜鉛、酸化ジルコニウム、酸化チタン(アナター
ス型)、酸化チタン(ルチル型)の二種以上の複合物か
ら選ばれる請求項1から3の何れかに記載の化粧料。
4. The inorganic white pigment in the organic-inorganic composite pigment is selected from two or more composites of zinc oxide, zirconium oxide, titanium oxide (anatase type) and titanium oxide (rutile type). The cosmetic according to any one of 3 above.
【請求項5】 炭酸アルカリ塩が炭酸ナトリウム、炭酸
カリウム、炭酸リチウムの一種又は二種以上から選ばれ
るものである請求項1から4の何れかに記載の化粧料。
5. The cosmetic according to claim 1, wherein the alkali carbonate is selected from one or more of sodium carbonate, potassium carbonate and lithium carbonate.
JP12052194A 1994-05-10 1994-05-10 Cosmetics containing organic-inorganic composite pigments Expired - Fee Related JP3241535B2 (en)

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JP3241535B2 JP3241535B2 (en) 2001-12-25

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Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2001098185A (en) * 1999-07-29 2001-04-10 Merck Japan Ltd Calcium carbonate-coated flaky pigment and method for producing the same
JP2005298515A (en) * 2004-04-08 2005-10-27 L'oreal Sa Set of two or more kinds of cake compositions for applying to skin, lip, nail and/or hair
JP2009029826A (en) * 2002-10-02 2009-02-12 L'oreal Sa Composition intended to be applied to skin and integument
JP2009114214A (en) * 2004-04-08 2009-05-28 L'oreal Sa Composition for applying to skin, lip, nail, and/or hair
JP2009120622A (en) * 2004-04-08 2009-06-04 L'oreal Sa Composition for application to skin, lip, nail, and/or hair
WO2011039952A1 (en) * 2009-09-30 2011-04-07 株式会社サンギ Method for improving the aqueous solubility of poorly-soluble substances
WO2012173000A1 (en) * 2011-06-13 2012-12-20 富士フイルム株式会社 Emulsion-type make-up base and method for producing same
US9248103B2 (en) 2012-03-02 2016-02-02 Kabushiki Kaisha Sangi Method for improving water solubility of slightly soluble substance
US9609934B2 (en) 2004-10-05 2017-04-04 L'oreal Method of applying makeup by means of a magnetic composition including at least one interferential pigment
US9649261B2 (en) 2004-10-05 2017-05-16 L'oreal Method of applying makeup to a surface and a kit for implementing such a method

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JPS56141362A (en) * 1980-04-04 1981-11-05 Pola Chem Ind Inc Lake pigment, its preparation and cosmetic comprising it
JPS6067407A (en) * 1983-09-22 1985-04-17 Pola Chem Ind Inc Cosmetic for make-up
JPS63152671A (en) * 1986-10-10 1988-06-25 ローヌープーラン・シミ Colored pigment, especially magnetic pigment, production thereof and use thereof especially in production of color forming powder
JPS63171678A (en) * 1987-01-06 1988-07-15 Shiseido Co Ltd Reformed solid material
JPS6442413A (en) * 1987-08-11 1989-02-14 Nippon Menaade Keshohin Kk Cosmetic
JPH01157908A (en) * 1987-12-14 1989-06-21 Tokuyama Soda Co Ltd Cosmetic
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Cited By (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2001098185A (en) * 1999-07-29 2001-04-10 Merck Japan Ltd Calcium carbonate-coated flaky pigment and method for producing the same
JP2009029826A (en) * 2002-10-02 2009-02-12 L'oreal Sa Composition intended to be applied to skin and integument
JP2005298515A (en) * 2004-04-08 2005-10-27 L'oreal Sa Set of two or more kinds of cake compositions for applying to skin, lip, nail and/or hair
JP2009114214A (en) * 2004-04-08 2009-05-28 L'oreal Sa Composition for applying to skin, lip, nail, and/or hair
JP2009120622A (en) * 2004-04-08 2009-06-04 L'oreal Sa Composition for application to skin, lip, nail, and/or hair
US9609934B2 (en) 2004-10-05 2017-04-04 L'oreal Method of applying makeup by means of a magnetic composition including at least one interferential pigment
US9649261B2 (en) 2004-10-05 2017-05-16 L'oreal Method of applying makeup to a surface and a kit for implementing such a method
WO2011039952A1 (en) * 2009-09-30 2011-04-07 株式会社サンギ Method for improving the aqueous solubility of poorly-soluble substances
JP5663750B2 (en) * 2009-09-30 2015-02-04 株式会社サンギ Method for improving water solubility of poorly soluble substances
US9023398B2 (en) 2009-09-30 2015-05-05 Kabushiki Kaisha Sangi Method for improving the aqueous solubility of poorly-soluble substances
WO2012173000A1 (en) * 2011-06-13 2012-12-20 富士フイルム株式会社 Emulsion-type make-up base and method for producing same
US9248103B2 (en) 2012-03-02 2016-02-02 Kabushiki Kaisha Sangi Method for improving water solubility of slightly soluble substance

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