JPH0454110A - Color pigment and cosmetic containing the same pigment - Google Patents

Color pigment and cosmetic containing the same pigment

Info

Publication number
JPH0454110A
JPH0454110A JP16544790A JP16544790A JPH0454110A JP H0454110 A JPH0454110 A JP H0454110A JP 16544790 A JP16544790 A JP 16544790A JP 16544790 A JP16544790 A JP 16544790A JP H0454110 A JPH0454110 A JP H0454110A
Authority
JP
Japan
Prior art keywords
powder
resin
pigment
cosmetic
color pigment
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
JP16544790A
Other languages
Japanese (ja)
Other versions
JP2958536B2 (en
Inventor
Takashi Someya
高士 染谷
Shinji Tanabe
田部 信二
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.)
Kose Corp
Original Assignee
Kose 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 Kose Corp filed Critical Kose Corp
Priority to JP16544790A priority Critical patent/JP2958536B2/en
Publication of JPH0454110A publication Critical patent/JPH0454110A/en
Application granted granted Critical
Publication of JP2958536B2 publication Critical patent/JP2958536B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Abstract

PURPOSE:To obtain yellow-based color pigment excellent in coloring properties, oil resistance, stability and safety, by at least partially coating the surface of powder with riboflavin butyrate and a resin and to obtain a cosmetic, especially makeup cosmetic, containing the color pigment. CONSTITUTION:The surface of powder comprising inorganic white pigment such as preferably talc, kaolin or mica, inorganic color pigment such as yellow iron oxide, organic powder such as nylon powder or cosmetic powder of pearl agent such as titanium mica, especially inorganic white powder is at least partially coated with riboflavin butyrate and a resin such as nitrocellulose, alkyd resin and/or acrylic resin capable of forming a water-resistant and oil resistant coating film by uniformly blending the powder with riboflavin in a solvent, removing the solvent and coating with the resin to give yellow-based color pigment having the above-mentioned effect and a cosmetic usable around mucosa of the eye.

Description

【発明の詳細な説明】 〔産業上の利用分野〕 本発明は発色性、耐油性、安定性及び安全性の高い黄色
系の着色顔料並びにこれを含有する化粧料に関する。
DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] The present invention relates to a yellow colored pigment with high color development, oil resistance, stability and safety, and cosmetics containing the same.

〔従来の技術〕[Conventional technology]

従来より化粧料、特にメーキャップ化粧料には着色剤と
して種々の着色顔料が配合されている。
BACKGROUND ART Cosmetics, especially makeup cosmetics, have conventionally contained various coloring pigments as colorants.

着色顔料としては通常タール系色素及び無機顔料が広く
用いられている。
Tar-based pigments and inorganic pigments are commonly used as coloring pigments.

〔発明が解決しようとする課題〕[Problem to be solved by the invention]

しかしながら、タール系色素は発色性が良好で、広範な
色調のものが存在するが、耐油性、安定性が充分でなく
、また安全性の面から眼粘膜周辺に用いる化粧料に使用
できない等の欠点があった。
However, although tar-based pigments have good coloring properties and are available in a wide range of colors, they do not have sufficient oil resistance or stability, and due to safety reasons, they cannot be used in cosmetics used around the eye mucous membranes. There were drawbacks.

一方、無機顔料は耐油性、安定性及び安全性には優れて
いるものの、色調において充分でないという欠点があっ
た。特に無機顔料には高彩度で黄色系の色調を有するも
のがなかった。
On the other hand, although inorganic pigments are excellent in oil resistance, stability, and safety, they have the disadvantage that they are insufficient in color tone. In particular, there was no inorganic pigment that had a yellowish tone with high chroma.

従って、耐油性、安定性、安全性及び発色性の良好な黄
色系の顔料の開発が望まれていた。
Therefore, it has been desired to develop a yellow pigment with good oil resistance, stability, safety, and color development.

〔課題を解決するための手段〕[Means to solve the problem]

かかる実情において、本発明者らは鋭意検討した結果、
粉体表面を、黄色の蛍光を有するビタミン日、誘導体で
あるリボフラビン酪酸エステル及び樹脂被覆すれば、耐
油性、安定性、安全性及び発色性の良好な顔料が得られ
、またこれを配合すれば優れた発色性、化粧持続性及び
使用感の良好な化粧料が得られることを見出し、本発明
を完成した。
Under these circumstances, as a result of intensive study, the inventors found that
If the surface of the powder is coated with a yellow fluorescent vitamin, a derivative of riboflavin butyrate, and a resin, a pigment with good oil resistance, stability, safety, and color development can be obtained. The present invention was completed based on the discovery that it is possible to obtain a cosmetic with excellent color development, long-lasting makeup, and good feeling of use.

すなわち、本発明は粉体表面の少なくとも一部がリボフ
ラビン酪酸エステル及び樹脂で被覆されていることを特
徴とする着色顔料、並びに当該着色顔料を含有すること
を特徴とする化粧料を提供するものである。
That is, the present invention provides a colored pigment characterized in that at least a part of the powder surface is coated with riboflavin butyrate and a resin, and a cosmetic characterized in that it contains the colored pigment. be.

本発明の着色顔料に用いられる粉体としては、特に限定
されないが、化粧料用粉体、例えばタルク、カオリン、
マイカ、炭酸マグネシウム、炭酸カルシウム、ケイ酸マ
グネシウム、ケイ酸アルミニウムマグネシウム、シリカ
、酸化チタン、酸化亜鉛、酸化アルミニウム等の無機体
質・白色顔料;黄酸化鉄等の無機有色顔料;ナイロン粉
末、ポリエチレン末、スチレンパウダー、ポリテトラフ
ルオロエチレンパウダー シルクパウダー、結晶セルロ
ース、N−ラウロイル−し−リジン等の有機粉末;雲母
チタン、酸化鉄雲母チタン、オキシ塩化ビスマス等のパ
ール剤等が好ましい。就中、無機体質・白色顔料が特に
好ましい。これら粉体は、化粧料等のその使用目的に応
じて、一種または二種以上を選択して用いられる。
The powder used in the colored pigment of the present invention is not particularly limited, but powder for cosmetics, such as talc, kaolin,
Inorganic white pigments such as mica, magnesium carbonate, calcium carbonate, magnesium silicate, magnesium aluminum silicate, silica, titanium oxide, zinc oxide, aluminum oxide; inorganic colored pigments such as yellow iron oxide; nylon powder, polyethylene powder, Organic powders such as styrene powder, polytetrafluoroethylene powder, silk powder, crystalline cellulose, and N-lauroyl-thi-lysine; pearl agents such as titanium mica, titanium iron mica oxide, and bismuth oxychloride are preferred. Among these, inorganic white pigments are particularly preferred. One or more of these powders may be selected and used depending on the purpose of use, such as cosmetics.

本発明に用いられるリボフラビン酪酸エステルはリボフ
ラビン(ビタミンB2)の酪酸エステルであり、黄色の
蛍光を有する。リボフラビン酪酸エステルは、本発明の
着色顔料において黄色蛍光発色源である。従って、粉体
として体質または白色粉体を用いれば本発明の着色顔料
は黄色となり、着色粉体を用いれば黄色と当該粉体との
混合色となる。
The riboflavin butyrate used in the present invention is a butyrate of riboflavin (vitamin B2) and has yellow fluorescence. Riboflavin butyrate is the yellow fluorescent color source in the colored pigments of the present invention. Therefore, if a body or white powder is used as the powder, the colored pigment of the present invention will be yellow, and if a colored powder is used, the color will be a mixture of yellow and the powder.

本発明に用いられる樹脂としては、溶剤中でリボフラビ
ン酪酸エステルと均一に混合し、当該溶剤を除去した後
、耐水・耐油性の被膜を形成し得るものであれば特に制
限されないが、例えばニトロセルロース、アルキッド樹
脂、アクリル樹脂等が挙げられる。またこれら樹脂は単
独でまたは二種以上を混合して用いることができる。
The resin used in the present invention is not particularly limited as long as it can be uniformly mixed with riboflavin butyrate in a solvent and form a water- and oil-resistant film after removing the solvent, but examples include nitrocellulose. , alkyd resin, acrylic resin, etc. Further, these resins can be used alone or in combination of two or more.

本発明の着色顔料は、例えばリボフラビン酪酸エステル
及び樹脂を適当な溶剤に溶解し、これを粉体と混合する
かまたは粉体に噴霧した後、溶剤を除去して得られた凝
集体を粉砕することにより製造される。ここで溶剤とし
ては、樹脂及びリボフラビン酪酸エステルを溶解するも
のであれば特に制限されないが、例えば酢酸エチル、酢
酸ブチル、トルエン、エタノール、キシレン、フロン等
の有機溶剤が挙げられる。この方法を実施するにあたっ
て原料の使用量は特に制限されないが、リボフラビン酪
酸エステルの濃度が低すぎると発色性が充分でなく、ま
た高すぎると耐油性、安定性に問題が生じることから、
樹脂1重量部に対して1/100〜1重量部のリボフラ
ビン酪酸エステルを用い、これら全体に対してlO〜1
00容量倍程度容量列程度い、リボフラビン醋酸エステ
ル1重量部に対し1〜100重量部の粉体を用いるのが
好ましい。また溶剤の除去は、好ましくは減圧下で50
〜80℃程度の加熱により行なわれる。
The colored pigment of the present invention can be produced by, for example, dissolving riboflavin butyrate and a resin in a suitable solvent, mixing this with powder or spraying it on the powder, and then removing the solvent and pulverizing the resulting aggregate. Manufactured by Here, the solvent is not particularly limited as long as it dissolves the resin and riboflavin butyrate, and examples thereof include organic solvents such as ethyl acetate, butyl acetate, toluene, ethanol, xylene, and chlorofluorocarbons. There are no particular restrictions on the amount of raw materials used in carrying out this method, but if the concentration of riboflavin butyrate is too low, the color development will not be sufficient, and if it is too high, problems will arise with oil resistance and stability.
Using 1/100 to 1 part by weight of riboflavin butyric acid ester to 1 part by weight of the resin, and lO to 1 part by weight for the entire
It is preferable to use the powder in an amount of 1 to 100 parts by weight per 1 part by weight of riboflavin acetic acid ester. Also, the removal of the solvent is preferably carried out under reduced pressure for 50 min.
This is done by heating to about 80°C.

このようにして得られた着色顔料は、黄色系であり、か
かる着色を希望する各種化粧料に配合することができる
。なお、本発明の着色顔料は粉体表面の全部がリボフラ
ビン酪酸エステル及び樹脂によって被覆されている必要
はなく、粉体表面の一部が被覆されていればよい。また
、本発明の着色顔料は、更に化粧料用粉体に一般に行な
われる表面処理、例えばシリコン処理、金属セッケン処
理等を施しても良い。
The colored pigment thus obtained has a yellow color and can be incorporated into various cosmetics that desire such coloring. In the colored pigment of the present invention, the entire powder surface does not need to be coated with the riboflavin butyrate and the resin, but only a part of the powder surface should be coated. Furthermore, the colored pigment of the present invention may be further subjected to surface treatments commonly applied to powders for cosmetics, such as silicon treatment and metal soap treatment.

本発明にかかる着色顔料を配合しうる化粧料は、製品形
態、形状を問わず、粉末状・プレス状・液状・スティッ
ク状何れのものでもよく、例示すれば、粉白粉、ファン
デーション、ホホ紅、アイシャドウ、口紅、アイライナ
ー、マスカラ、アイブロウ、顆粒状洗顔料等が挙げられ
る。
Cosmetics that can be blended with the colored pigments of the present invention may be powdered, pressed, liquid, or stick, regardless of the product form or shape. Examples include eye shadow, lipstick, eyeliner, mascara, eyebrow, granular facial cleanser, etc.

化粧料への本発明の着色顔料の配合量は、製品の種類・
形態等に応じ、特に限定されるものではないが、好まし
くは1〜99重量%の範囲内である。
The amount of the coloring pigment of the present invention added to cosmetics depends on the type of product and
Although not particularly limited depending on the form etc., it is preferably within the range of 1 to 99% by weight.

着色顔料の配合にあたっては、単独の粉体に被覆処理を
施した着色顔料を化粧料中に配合しても良く、また化粧
料の粉体系全体に被覆処理を施しても良い。
When blending the colored pigment, a colored pigment obtained by coating a single powder may be blended into the cosmetic, or the entire powder system of the cosmetic may be coated.

本発明の化粧料には、上記着色顔料の他、通常化粧料に
用いられる他の成分として、通常の白色・体質・着色顔
料、パール剤、有機粉末、油剤、金属セッケン、界面活
性剤、保湿剤、アルコール、pH調整剤、防腐剤、酸化
防止剤、紫外線吸収剤、水溶性高分子、キレート剤、美
容成分、香料、その地番種添加剤等から適宜選択して配
合することができる。
In addition to the coloring pigments mentioned above, the cosmetics of the present invention include other ingredients normally used in cosmetics, such as normal white, body, and coloring pigments, pearl agents, organic powders, oils, metal soaps, surfactants, and moisturizers. They can be appropriately selected and blended from agents, alcohols, pH adjusters, preservatives, antioxidants, ultraviolet absorbers, water-soluble polymers, chelating agents, cosmetic ingredients, fragrances, and additives based on their lot numbers.

〔実施例〕〔Example〕

次に実施例を挙げて本発明を更に詳細に説明するが、こ
れらは本発明を何ら限定するものではない。
EXAMPLES Next, the present invention will be explained in more detail with reference to Examples, but these are not intended to limit the present invention in any way.

試験例 第1表に示す組成の着色顔料を調製し、その発色性、耐
油性、染着性及び安定性試験を行った。
Test Example Colored pigments having the compositions shown in Table 1 were prepared and tested for color development, oil resistance, dyeability and stability.

なお、試験にあたっては、着色顔料87重量部にミリス
チン酸イソプロピル5.0重量部及び流動パラフィン8
.0重量部を加えて調製した試料を用いた。
In addition, in the test, 87 parts by weight of color pigment, 5.0 parts by weight of isopropyl myristate, and 8 parts by weight of liquid paraffin were added.
.. A sample prepared by adding 0 parts by weight was used.

く着色顔料の製造法〉 リボフラビン酪酸エステル及び樹脂を酢酸エチル100
重量部に溶解し、これに粉体を加えて混合する。次いで
これを減圧下70℃に加熱して酢酸エチルを揮散させた
後粉砕する。
Production method of colored pigment> Riboflavin butyrate and resin are mixed with 100% ethyl acetate.
Dissolve in parts by weight, add powder to this and mix. Next, this is heated to 70° C. under reduced pressure to volatilize ethyl acetate, and then pulverized.

なお、黄色4号アルミニウムレーキはマイカと混合後粉
砕した。
Note that yellow No. 4 aluminum lake was mixed with mica and then ground.

く試験方法〉 (1)発色性 日本重色色差計SZ−Σ80をを用いてマンセル彩度を
測定した。
Test Method> (1) Chromogenicity Munsell chroma was measured using a Nihon Heavy Color Difference Meter SZ-Σ80.

(2)耐油性 試験管に試料1部及びミリスチン酸イソプロピル10部
をとり、30回振止うし、2時間静置後上澄みについて
400nmにおける透過性を測定した。
(2) 1 part of the sample and 10 parts of isopropyl myristate were placed in an oil-resistant test tube, shaken 30 times, and allowed to stand for 2 hours, after which the transmittance at 400 nm of the supernatant was measured.

(3)染着性 試料を皮膚に塗布し、半日後ふき取り、顔料の皮膚への
染着性を観察した。
(3) Dyeability The sample was applied to the skin, and after half a day, it was wiped off and the dyeability of the pigment to the skin was observed.

(4)安定性 試料をプレス成型して、50℃1ケ月後のにじみ状態を
観察した。
(4) Stability Samples were press-molded and the state of bleeding was observed after one month at 50°C.

(5)安全性 実施例1.2及び比較例1〜3の着色顔料が眼粘膜で使
用できるか否かを評価した。
(5) Safety It was evaluated whether the colored pigments of Example 1.2 and Comparative Examples 1 to 3 could be used on the ocular mucosa.

〈結果〉 結果を第1表に示す。<result> The results are shown in Table 1.

実施例1  アイシャドウ (重1B) 1、タルク             34.92、カ
オリン            153、炭酸マグネシ
ウム         14、ステアリン酸亜鉛   
     105、酸化チタン           
56、マイカ             157、リボ
フラビン酪酸エステル    0.98、アルキッド樹
脂          2.89、群青       
        310、雲母チタン        
    711、ソルビタンセスキオレート     
112、流動パラフィン         413、ラ
ノリン              114、防腐剤 
            適量(製法) ANα7.8を酢酸エチル60重量部に溶解し、これに
Nα1〜6を加え混合する。
Example 1 Eyeshadow (heavy 1B) 1, talc 34.92, kaolin 153, magnesium carbonate 14, zinc stearate
105, titanium oxide
56, mica 157, riboflavin butyrate 0.98, alkyd resin 2.89, ultramarine blue
310, mica titanium
711, sorbitan sesquiolate
112, Liquid paraffin 413, Lanolin 114, Preservative
Appropriate amount (manufacturing method) ANα7.8 is dissolved in 60 parts by weight of ethyl acetate, and Nα1 to 6 are added thereto and mixed.

BAを加熱して酢酸エチルを蒸発揮散させる。BA is heated to evaporate and evaporate ethyl acetate.

CBにNα9.10を加え、混合粉砕する。Add Nα9.10 to CB and mix and grind.

D  Nn11〜14を加熱溶解後、Cを加え混合し、
プレス成型してアイシャドウを得る。
D After heating and dissolving Nn11 to 14, add C and mix,
Press mold to obtain eyeshadow.

上記の如くして得られたアイシャドウは、皮膚への染着
がなく、従来にない発色性を有し、かつ色にじみ等の色
変化がなく、化粧持続性、使用感共に良好なものであっ
た。
The eye shadow obtained as described above does not stain the skin, has unprecedented color development, does not cause color bleeding or other color changes, and has good makeup durability and usability. there were.

実施例2  ファンデーション マイカ リボフラビン酪酸エステル アルキッド樹脂 酸化チタン コロイダルカオリン タルク 黒酸化鉄 ベンガラ 黄酸化鉄 流動パラフィン ソルビタンセスキオレート (重量部) 8.2 0.3 1.5 33.4 0.6 1.5 3.5 12、グリセリン          313、香 料
             適量14、防腐剤    
         適量(製法) ANα2.3をエタノール30重量部に溶解し、これに
Nα1を加え混合する。
Example 2 Foundation Micariboflavin butyrate ester alkyd resin Titanium oxide colloidal kaolin talc Black iron oxide Red iron oxide Yellow iron oxide Liquid paraffin Sorbitan sesquiolate (parts by weight) 8.2 0.3 1.5 33.4 0.6 1.5 3 .5 12, glycerin 313, fragrance appropriate amount 14, preservative
Appropriate amount (manufacturing method) ANα2.3 is dissolved in 30 parts by weight of ethanol, and Nα1 is added thereto and mixed.

BAを加熱してエタノールを蒸発揮散させる。BA is heated to evaporate and evaporate ethanol.

CBにNα4〜9を加え、混合粉砕する。Add Nα4 to 9 to CB and mix and pulverize.

D  Nn11〜14を加熱溶解後、Cを加え混合し、
プレス成型してファンデーションを得る。
D After heating and dissolving Nn11 to 14, add C and mix,
Press mold to obtain foundation.

上記の如くして得られたファンデーションは、皮膚への
染着かなく、化粧持続性、使用感共に良好なものであっ
た。
The foundation obtained as described above did not stain the skin, had good makeup persistence, and had good feel on use.

実施例3  口紅 1、タルク 2、リボフラビン酪酸エステル 3、ニトロセルロース 4、ヒマシ油 5、ヘキサデシルアルコール (重量部) 0.2 1.5 6、ラノリン             47、ミツロ
ウ             58、オシケライト  
         49、キャンデリラロウ     
    710、カルナウバロウ          
211、酸化防止剤           適量12、
防腐剤             適量13゜香 料 
            適量14、酸化チタン   
        215、赤色226号       
     1(製法) ANcL2.3をキシレン40重量部に溶解し、これに
N(L 1を加え混合する。
Example 3 Lipstick 1, talc 2, riboflavin butyrate 3, nitrocellulose 4, castor oil 5, hexadecyl alcohol (parts by weight) 0.2 1.5 6, lanolin 47, beeswax 58, oshikelite
49, Candelilla Row
710, Carnauba Row
211, Antioxidant appropriate amount 12,
Preservatives Appropriate amount 13°Fragrance
Appropriate amount 14, titanium oxide
215, red No. 226
1 (Production method) ANcL2.3 is dissolved in 40 parts by weight of xylene, and N(L1) is added thereto and mixed.

BAを加熱してキシレンを蒸発揮散させた後、粉砕する
BA is heated to evaporate and evaporate xylene, and then pulverized.

Nα4〜12を加熱溶解する。Heat and dissolve Nα4-12.

DCにB及びNα14.15を混練した後、再溶解し、
k13を加え、脱泡する。
After kneading B and Nα14.15 in DC, redissolve it,
Add k13 and defoam.

EDを容器に充填成型して、口紅を得る。A lipstick is obtained by filling and molding the ED into a container.

上記の如くして得られた口紅は、皮膚への染着がなく、
従来にない発色性を有し、かつ色にじみ等の色変化がな
く、化粧持続性、使用感共に良好なものであった。
The lipstick obtained as described above does not stain the skin,
It had unprecedented color development, was free of color changes such as color bleeding, and had good makeup durability and usability.

実施例4  マスカラ (重量部) 1、マイカ             2.52、タル
ク              23、リボフラビン酪
酸エステル    0.14、ニトロセルロース   
      0.45、カルナウバロウ       
  76、ミツロウ             27、
マイクロクリスタリンワックス  208 ラノリン 
             0.49、流動ポリイソブ
チレン      60,610、ベンガラ     
         211、黒酸化鉄        
     212、防腐剤             
適量(製法) AN(L3.4をトルエン70重量部に溶解し、これに
Nα1.2を加え、混合する。
Example 4 Mascara (parts by weight) 1, mica 2.52, talc 23, riboflavin butyrate 0.14, nitrocellulose
0.45, carnauba wax
76, beeswax 27,
Microcrystalline wax 208 lanolin
0.49, fluid polyisobutylene 60,610, red iron
211, black iron oxide
212, preservatives
Appropriate amount (manufacturing method) Dissolve AN (L3.4) in 70 parts by weight of toluene, add Nα1.2 to this, and mix.

BAを加熱してトルエンを蒸発揮散させる。BA is heated to evaporate and evaporate toluene.

CNα5〜9及び12を加熱溶解する。CNα5-9 and 12 are heated and dissolved.

DBにN[Llo、11を加え、混合粉砕する。Add N[Llo, 11 to DB and mix and grind.

ECとDを混合分散し、容器に充填してマスカラを得た
EC and D were mixed and dispersed and filled into a container to obtain mascara.

上記の如くして得られたマスカラは、皮膚への染着がな
く、化粧持続性、使用感共に良好なものであった。
The mascara obtained as described above did not stain the skin and had good makeup durability and feel when used.

実施例5  ホホ紅 雲母チタン リボフラビン酪酸エステル アクリル樹脂 タルク カオリン 酸化チタン ステアリン酸亜鉛 コメデンプン 赤色202号 流動パラフィン (重量8) 0.5 3.5 52.2 0.8 11、香 料             適量(製法) ANα2.3をフロン11350重量部に溶解し、これ
をNα1に加え、混合する。
Example 5 Red mica titanium riboflavin butyrate ester acrylic resin talcum kaolin oxide titanium zinc stearate rice starch Red No. 202 liquid paraffin (weight 8) 0.5 3.5 52.2 0.8 11, fragrance appropriate amount (manufacturing method) ANα2.3 is dissolved in 11,350 parts by weight of Freon, and this is added to Nα1 and mixed.

BAを加熱してフロン113を蒸発揮散させる。BA is heated to evaporate and evaporate Freon 113.

CBにNα4〜9を加え、混合粉砕する。Add Nα4 to 9 to CB and mix and pulverize.

DNα10.11を混合溶解する。Mix and dissolve DNα10.11.

ECとDを混合し、プレス成型してホホ紅を得た。EC and D were mixed and press-molded to obtain red bean paste.

上記の如くして得られたホホ紅は、皮膚への染着がなく
、従来にない発色性を有し、かつ色にじみ等の色変化が
なく、化粧持続性、使用感共に良好なものであった。
The cheek beni obtained as described above does not stain the skin, has unprecedented coloring properties, does not cause color bleeding or other color changes, and has good makeup durability and usability. there were.

〔発明の効果〕〔Effect of the invention〕

本発明によれば発色性、耐油性、安定性及び安全性に優
れた黄色系の着色顔料が得られ、これを用いれば眼粘膜
周辺等にも使用し得る化粧料の提供が可能となった。
According to the present invention, a yellow colored pigment with excellent color development, oil resistance, stability, and safety can be obtained, and by using this, it is possible to provide a cosmetic that can be used around the mucous membrane of the eye, etc. .

以上 手続補正書(自発) 平成2年特許願第165447号 2、発明の名称 4、代 理 人 平成3年6月17日 6、補正の対象 明細書の「発明の詳細な説明」の欄 7、補正の内容 (1)明細書中、第7頁第15〜20行「リボフラビン
酪酸・・・・・粉砕した。」とあるを 「試験例1.2 ANα4.5を酢酸エチル100重量部に溶解し、これ
にNα1〜3を加えて混合する。
Written amendment to the above procedures (voluntary) Patent Application No. 165447 of 1990 2, Title of the invention 4, Attorney dated June 17, 1991 6, "Detailed description of the invention" column 7 of the specification subject to amendment, Contents of amendment (1) In the specification, page 7, lines 15 to 20, "Riboflavin butyric acid...pulverized" was replaced with "Test Example 1.2 ANα4.5 was dissolved in 100 parts by weight of ethyl acetate." Then, add Nα1 to Nα3 and mix.

BAを減圧下70℃に加熱して酢酸エチルを揮散させる
BA is heated to 70° C. under reduced pressure to volatilize the ethyl acetate.

CBを粉砕して着色顔料を得る。CB is ground to obtain colored pigments.

比較例I ANα1.4を混合、粉砕して着色顔料を得る。Comparative example I A colored pigment is obtained by mixing and pulverizing ANα1.4.

比較例2 A  No、4を酢酸エチル100重量部に溶解し、こ
れにNα1を加えて混合する。
Comparative Example 2 A No. 4 was dissolved in 100 parts by weight of ethyl acetate, and Nα1 was added thereto and mixed.

BAを減圧下70℃に加熱して酢酸エチルを揮散させる
BA is heated to 70° C. under reduced pressure to volatilize the ethyl acetate.

CBを粉砕して着色顔料を得る。CB is ground to obtain colored pigments.

比較例3 ANα1.6を混合、粉砕して着色顔料を得る。」と訂
正する。
Comparative Example 3 A colored pigment is obtained by mixing and pulverizing ANα1.6. ” he corrected.

(2)同第8頁第8行 r400nmJとあるを r440nmJと訂正する。(2) Page 8, line 8 It says r400nmJ. Corrected to r440nmJ.

Claims (1)

【特許請求の範囲】 1、粉体表面の少なくとも一部がリボフラビン酪酸エス
テル及び樹脂で被覆されていることを特徴とする着色顔
料。 2、請求項1記載の着色顔料を含有することを特徴とす
る化粧料。
[Scope of Claims] 1. A colored pigment characterized in that at least a part of the powder surface is coated with riboflavin butyrate and a resin. 2. A cosmetic containing the colored pigment according to claim 1.
JP16544790A 1990-06-22 1990-06-22 Color pigments and cosmetics containing the same Expired - Fee Related JP2958536B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP16544790A JP2958536B2 (en) 1990-06-22 1990-06-22 Color pigments and cosmetics containing the same

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP16544790A JP2958536B2 (en) 1990-06-22 1990-06-22 Color pigments and cosmetics containing the same

Publications (2)

Publication Number Publication Date
JPH0454110A true JPH0454110A (en) 1992-02-21
JP2958536B2 JP2958536B2 (en) 1999-10-06

Family

ID=15812602

Family Applications (1)

Application Number Title Priority Date Filing Date
JP16544790A Expired - Fee Related JP2958536B2 (en) 1990-06-22 1990-06-22 Color pigments and cosmetics containing the same

Country Status (1)

Country Link
JP (1) JP2958536B2 (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2005087182A1 (en) * 2004-03-17 2005-09-22 Kabushiki Kaisha Hayashibara Seibutsu Kagaku Kenkyujo Functional powders
JP2008050312A (en) * 2006-08-25 2008-03-06 Avon Products Inc Skin tone concealer for use in cosmetic and cosmetic containing the same

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2005087182A1 (en) * 2004-03-17 2005-09-22 Kabushiki Kaisha Hayashibara Seibutsu Kagaku Kenkyujo Functional powders
US8841261B2 (en) 2004-03-17 2014-09-23 Hayashibara Co., Ltd. Functional powdery product
JP2008050312A (en) * 2006-08-25 2008-03-06 Avon Products Inc Skin tone concealer for use in cosmetic and cosmetic containing the same

Also Published As

Publication number Publication date
JP2958536B2 (en) 1999-10-06

Similar Documents

Publication Publication Date Title
US4988502A (en) Mascara composition
AU646690B2 (en) Coated cosmetic materials and method of coating cosmetic materials
JPS61277606A (en) Cosmetic composition
JP2993934B2 (en) Novel cosmetic composition containing film-forming polymer
JPH0524124B2 (en)
EP3166576B1 (en) Cosmetic composition
JPH0222728B2 (en)
JPH04128211A (en) Ground cosmetic
US5221342A (en) Coloring composition and production method and use thereof
JPH1112493A (en) Composite powder and composition containing the same
JP2630428B2 (en) Color pigments and cosmetics containing the same
JPH0454110A (en) Color pigment and cosmetic containing the same pigment
JP4412673B2 (en) Water base lip cosmetic and makeup method
JPH0729905B2 (en) Manufacturing method of powder solid cosmetics
JPH01172312A (en) Cosmetic
JP2000302625A (en) Solid powder cosmetic
JP2004307409A (en) Pigment for cosmetic and cosmetic containing the same
JP3409191B2 (en) Lipstick composition
JPS61194011A (en) Makeup cosmetic
JP2003012459A (en) Cosmetic
JPH03236307A (en) Oily cosmetic
JP3527017B2 (en) Oily solid cosmetics
JPH05238914A (en) Emulsified cosmetic pack
JPS62298511A (en) Makeup cosmetic
KR102334447B1 (en) Non-press type solid cosmetic composition comprising polyethylene terephthalate based pearl powder

Legal Events

Date Code Title Description
LAPS Cancellation because of no payment of annual fees