JPS6248642B2 - - Google Patents

Info

Publication number
JPS6248642B2
JPS6248642B2 JP498980A JP498980A JPS6248642B2 JP S6248642 B2 JPS6248642 B2 JP S6248642B2 JP 498980 A JP498980 A JP 498980A JP 498980 A JP498980 A JP 498980A JP S6248642 B2 JPS6248642 B2 JP S6248642B2
Authority
JP
Japan
Prior art keywords
pigment
water
rhodamine
added
cosmetics
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
Application number
JP498980A
Other languages
Japanese (ja)
Other versions
JPS56103105A (en
Inventor
Masako Nakamura
Muneo Tanaka
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Shiseido Co Ltd
Original Assignee
Shiseido Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Shiseido Co Ltd filed Critical Shiseido Co Ltd
Priority to JP498980A priority Critical patent/JPS56103105A/en
Publication of JPS56103105A publication Critical patent/JPS56103105A/en
Publication of JPS6248642B2 publication Critical patent/JPS6248642B2/ja
Granted legal-status Critical Current

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q1/00Make-up preparations; Body powders; Preparations for removing make-up
    • A61Q1/02Preparations containing skin colorants, e.g. pigments
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/49Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds
    • A61K8/4973Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with oxygen as the only hetero atom
    • A61K8/498Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with oxygen as the only hetero atom having 6-membered rings or their condensed derivatives, e.g. coumarin

Landscapes

  • Life Sciences & Earth Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Birds (AREA)
  • Epidemiology (AREA)
  • Cosmetics (AREA)

Description

【発明の詳細な説明】[Detailed description of the invention]

本発明は、粘度鉱物にローダミンB、多価金属
イオン及び水溶性高分子を吸着させて得られる、
色相を黄味に調整した赤色系着色顔料を化粧料基
剤に配合して得られる化粧料、特にメイクアツプ
化粧料に関する。 従来、カチオン染料であるローダミンBを顔料
化して化粧料特にメイクアツプ化粧料に使用しよ
うとする試みが、業界において種々行なわれてい
る。 たとえば、カチオン交換能を有する粘度鉱物に
ローダミンBを結合させた顔料が公知である。し
かしながら、このものは皮膚への染着性はないも
のの、色調が青味の赤色であり、さらに彩度が低
くなるというローダミンB本来が有する鮮明な色
調をつぶしてしまうという新たな欠点をも持つて
いる。従つてこのものを化粧料に用いた場合、彩
度が低い上に化粧料特にメイクアツプ化粧料が必
要としている赤味がだせず、実際には使用できな
い。 さらに、カチオン交換能を有する粘度鉱物に界
面活性剤で色相を調整したローダミンB及び多価
金属イオンを結合して得られる赤色系顔料組成物
も公知である。しかしながら、このものは皮膚へ
の染着性のない色彩効果のすぐれた顔料である
が、青味が強く、化粧料特にメイクアツプ化粧料
に使用するには黄味が不足しており、従つて実際
には化粧料への配合ができない。さらに調整剤と
して用いている界面活性剤は、中でも非イオン界
面活性剤が比較的刺激が少ないものの皮膚への安
全性の面で危具がないとはいえない。 本発明者らは、これらの欠点を改良すべく鋭意
研究を重ねた結果、皮膚への安全性の全く問題の
ない水溶性高分子を中心としたもので処理するこ
とにより、種々欠点を補なつた黄味に調整した赤
色系着色顔料を用いた化粧料を見い出し本発明を
完成するに至つた。 すなわち本発明は、カチオン交換能を有する粘
土鉱物に、ローダミンBと多価金属イオンと水溶
性高分子を吸着させて得られる、色相を黄味に調
整した赤色系着色顔料を配合したことを特徴とす
る化粧料を提供するものである。 次に本発明に用いられる着色顔料について説明
する。処理剤として用いられる水溶性高分子は天
然物でも合成物でもよい。 例えば、ゼラチン、カゼイン、等の動物系高分
子、デンプン類、植物ガム質、海そう類、植物粘
液質等の植物系高分子、ケルトロール等の微生物
多糖類、メチルセルロース、カルボキシメチルセ
ルロースナトリウム塩、ヒドロキシエチルセルロ
ース等のセルロース誘導体、ポリビニルアルコー
ル、ポリビニルピロリドン、ポリアクリル酸誘導
体、ポリメタクリル酸誘導体等のビニル系高分
子、ポリエチレンオキシド等をあげることができ
る。 水溶性高分子の配合量は、目的とする黄味に調
整した赤色系顔料を得るためには粘土鉱物に対し
て1〜50%配合するのが適当である。 粘土鉱物としては、カチオン交換能をもつモン
モリロナイト、ヘクトライト、ゼオライト、カオ
リン、ハロサイト、イライト等いずれも可能であ
るが、特に合成品であるラポナイトCPは白色粉
体であることから体質として優れたものである。 多価金属塩は、カルシウム、バリウム、亜鉛、
マンガン、アルミニウム、マグネシウム等の塩酸
塩、流酸塩等が用いられる。 本発明に用いられる着色顔料は、以下のいずれ
の方法をとつても得られる。 (1) 予めローダミンBの染料水溶液を調整した中
へ、粘土鉱物を除々に分散させていき均一に膨
潤する迄撹拌し続けた後、水溶性高分子物質で
処理する。 その後、更に多価金属で処理すると非膨潤型
の顔料が沈殿してくる。 (2) 予めローダミンBの染料水溶液を調整した中
へ、粘度鉱物を除々に分散させていき均一に膨
潤する迄撹拌し続けた後、多価金属で処理し、
次いで水溶性高分子物質で処理することにより
皮膚染着性のない、しかし色彩効果の優れた着
色顔料を得る。 次に具体例を持つて合成法を説明する。 合成例 1 予めラポナイトCP10gを、水500ml中に均一に
なる迄分散させた後、これとは別に0.2%ローダ
ミンB染料水溶液500mlを調整した溶液を上記分
散液に添加した。これを50℃、30分撹拌後、ポリ
ビニルピロリドン0.5gを加え、更に塩化カルシ
ウムで50℃、30分撹拌処理した。沈殿分離した非
膨潤型の着色顔料をろ過、水洗、乾燥、粉砕を行
ない目的の顔料を得た。 合成例 2 10gのラポナイトCPを水500ml中に均一に分散
させた液に、0.2%ローダミンB染料水溶液500ml
を添加し、50℃、30分撹拌した。 ついで塩化カルシウムを添加し、さらにポリビ
ニルピロリドン0.5gを加え、50℃、30分撹拌し
た。以下合成例1と同様にして目的顔料を得た。 次に本発明に用いられる顔料特性を示すが、そ
れに先立ち0.2%ローダミンB水溶液500mlに水溶
性高分子0.5gを添加した時の可視スペクトルを
測定し、主波長の変化を表1に示した。
The present invention is obtained by adsorbing rhodamine B, polyvalent metal ions, and water-soluble polymers to clay minerals.
The present invention relates to cosmetics, particularly make-up cosmetics, obtained by blending a red colored pigment with a yellowish hue into a cosmetic base. Conventionally, various attempts have been made in the industry to turn Rhodamine B, a cationic dye, into a pigment and use it in cosmetics, particularly make-up cosmetics. For example, a pigment in which rhodamine B is bonded to a clay mineral having cation exchange ability is known. However, although this product does not stain the skin, it has a bluish-red color tone, and it also has a new drawback that the saturation is low, which destroys the vivid color tone that Rhodamine B originally has. ing. Therefore, when this product is used in cosmetics, it has low chroma and cannot produce the reddish tinge required for cosmetics, especially makeup cosmetics, so it cannot be used in practice. Furthermore, a red pigment composition obtained by bonding rhodamine B whose hue has been adjusted with a surfactant and polyvalent metal ions to a clay mineral having cation exchange ability is also known. However, although this pigment has excellent color effects and does not stain the skin, it has a strong blue tint and lacks yellow tint for use in cosmetics, especially make-up cosmetics. cannot be incorporated into cosmetics. Furthermore, among the surfactants used as conditioning agents, nonionic surfactants are relatively less irritating, but they cannot be said to be without risks in terms of safety to the skin. As a result of intensive research to improve these drawbacks, the present inventors have found that they have been able to compensate for various drawbacks by treating the skin with mainly water-soluble polymers that have no safety issues at all. The present inventors have discovered a cosmetic material using a red colored pigment adjusted to have a yellowish tinge, and have completed the present invention. That is, the present invention is characterized by blending a red colored pigment with a yellowish hue obtained by adsorbing rhodamine B, polyvalent metal ions, and water-soluble polymers to clay minerals having cation exchange ability. The purpose of the present invention is to provide cosmetics that have the following properties. Next, the colored pigment used in the present invention will be explained. The water-soluble polymer used as a treatment agent may be a natural product or a synthetic product. For example, animal-based polymers such as gelatin and casein, starches, plant-based polymers such as plant gums, seaweeds, and plant mucilages, microbial polysaccharides such as Keltrol, methylcellulose, carboxymethylcellulose sodium salt, and hydroxyethylcellulose. Examples include cellulose derivatives such as, polyvinyl alcohol, polyvinylpyrrolidone, vinyl polymers such as polyacrylic acid derivatives, polymethacrylic acid derivatives, and polyethylene oxide. The appropriate amount of the water-soluble polymer to be blended is 1 to 50% based on the clay mineral in order to obtain a red pigment with the desired yellow tint. As clay minerals, montmorillonite, hectorite, zeolite, kaolin, hallosite, illite, etc., all of which have cation exchange ability, are possible, but Laponite CP, which is a synthetic product, has an excellent physical constitution because it is a white powder. It is something. Polyvalent metal salts include calcium, barium, zinc,
Hydrochlorides, hydrochlorides, etc. of manganese, aluminum, magnesium, etc. are used. The colored pigment used in the present invention can be obtained by any of the following methods. (1) Clay minerals are gradually dispersed into an aqueous Rhodamine B dye solution prepared in advance, and the mixture is stirred until uniformly swollen, and then treated with a water-soluble polymeric substance. Thereafter, when the material is further treated with a polyvalent metal, non-swellable pigments precipitate. (2) Gradually disperse the clay mineral into an aqueous rhodamine B dye solution prepared in advance and continue stirring until it swells uniformly, then treat it with a polyvalent metal,
Then, by treatment with a water-soluble polymeric substance, a colored pigment that does not stain the skin but has excellent color effects is obtained. Next, the synthesis method will be explained using a specific example. Synthesis Example 1 10 g of Laponite CP was previously dispersed in 500 ml of water until it became homogeneous, and a separate solution of 500 ml of a 0.2% rhodamine B dye aqueous solution was added to the above dispersion. After stirring this at 50°C for 30 minutes, 0.5 g of polyvinylpyrrolidone was added, and the mixture was further stirred with calcium chloride at 50°C for 30 minutes. The precipitated and separated non-swelling colored pigment was filtered, washed with water, dried and pulverized to obtain the desired pigment. Synthesis Example 2 Add 500 ml of 0.2% Rhodamine B dye aqueous solution to a solution in which 10 g of Laponite CP is uniformly dispersed in 500 ml of water.
was added and stirred at 50°C for 30 minutes. Then, calcium chloride was added, and then 0.5 g of polyvinylpyrrolidone was added, followed by stirring at 50°C for 30 minutes. The target pigment was obtained in the same manner as in Synthesis Example 1. Next, the characteristics of the pigment used in the present invention will be shown. Prior to that, the visible spectrum was measured when 0.5 g of water-soluble polymer was added to 500 ml of 0.2% rhodamine B aqueous solution, and the change in the dominant wavelength is shown in Table 1.

【表】 表1より、水溶性高分子を添加したものは無添
加のものに比べ明らかに主波長が短波長側へ移行
し、青味の赤から黄味の赤へと色調調整の効果が
表われている。 合成例1に準じて得られた着色顔料の色調、着
色力、及び水へのブリード性について示す。 着色顔料の色調は顔料粉末そのものを、又、着
色力については、着色顔料の一定量にヒマシ油一
定量を添加し、更に酸化チタンを着色顔料に対し
て適宜加え、ドクターブレードにて混練した後、
隠蔽率試験紙上に一定塗膜に塗布した。 これを分光光度計(日立カラーアナライザー
607型)にて測色し、得られたX,Y,ZをH.V.
Cマンセル値に換算し、更に着色力を表わす
Godloveの濃度式S=√1622に代入した。 ここで(=10−V)は暗度に相当し、S値は
大きい程着色力が大なることを表わす尺度とな
る。ブリード性については、着色顔料1gを採取
し、水で100gとし、1時間撹拌静置後、上澄液
を口過して日立340型自記分光光度計にて吸光度
(ε)を測定した。 以上の結果を着色顔料の粉末色については表2
に、ブリドー性については表3に、また着色力に
ついては図1に示した。
[Table] From Table 1, it is clear that the dominant wavelength of the water-soluble polymer-added product shifts to the shorter wavelength side compared to the additive-free product, and the color tone adjustment effect changes from bluish red to yellowish red. It's showing up. The color tone, coloring power, and bleedability into water of the colored pigment obtained according to Synthesis Example 1 are shown below. The color tone of the coloring pigment can be determined by using the pigment powder itself, and for the coloring power, a certain amount of castor oil is added to a certain amount of the coloring pigment, titanium oxide is added as appropriate to the coloring pigment, and the mixture is kneaded with a doctor blade. ,
A constant coating was applied onto a hiding rate test paper. This is measured using a spectrophotometer (Hitachi Color Analyzer).
607 type), and the obtained X, Y, Z are HV
C Convert to Munsell value and further express coloring power
Substituted into Godlove's concentration formula S=√16 2 + 2 . Here, (=10-V) corresponds to darkness, and the larger the S value is, the greater the coloring power is. Regarding the bleeding property, 1 g of the colored pigment was collected, diluted to 100 g with water, stirred and left to stand for 1 hour, and the supernatant liquid was passed through the mouth and the absorbance (ε) was measured using a Hitachi 340 self-recording spectrophotometer. The above results are summarized in Table 2 for the powder color of the colored pigment.
In addition, the bleed properties are shown in Table 3, and the tinting power is shown in Figure 1.

【表】【table】

【表】 表2、表3より明らかなように、水溶性高分子
処理することにより色相は黄味に寄り採度も向上
し、しかもブリード性のない良好な顔料である。 また、着色力は図1から明らかなように、水溶
性高分子無添加品よりも大きな値をとつている。 なお、合成例2の方法に準じて得られた着色顔
料についてもほぼ同じ結果が得られた。 次に本発明の実施例を示す。(配合量は重量部
を示す。) 実施例 1 モンモリロナイト100gを水5中に均一に分
散させた中に、ローダミンB10gを水1中に溶
解させた液を添加し、50℃、30分撹拌した。 その後0.5gのポリビニルピロリドンの溶解さ
せた300ml溶液を加え、さらに0.2Nの塩化カルシ
ウム100mlを添加し、50℃、30分撹拌した。沈殿
分離物をろ過し、水洗、乾燥、粉砕の工程を経て
着色顔料を得た。得られた顔料をネイルエナメル
中に配合した。 ニトロセルロース(1/2秒) 10.0 アルキツド樹脂 10.0 クエン酸アセチルトリブチル 5.0 酢酸エチル 20.0 酢酸ブチル 15.0 エチルアルコール 5.0 トルエン 35.0 着色顔料 適 量 沈殿防止剤 〃 実施例 2 ラポナイトCP100gを水5中に均一分散させ
た中に、ローダミンB20gを1中に溶解させた
液を添加し、50℃、30分撹拌した。 ついで0.2Nの塩化アルミニウム100mlを添加
し、さらに0.5gのカルボキシメチルセルロース
ナトリウム塩を溶解させた100ml溶液を加え、50
℃、30分撹拌した。以下実施例1と同様にして顔
料を得た。得られた顔料を口紅に配合した。 カルナウバロウ 16.0 オゾケライト 16.0 ラノリン 24.0 流動パラフイン 24.0 ブチルステアレート 10.0 着色顔料 6.0 酸化チタン 4.0 香 料 適 量 酸化防止剤 〃
[Table] As is clear from Tables 2 and 3, the hue becomes more yellowish and the pigmentation is improved by the water-soluble polymer treatment, and it is a good pigment with no bleeding properties. Furthermore, as is clear from FIG. 1, the coloring power is higher than that of the product without water-soluble polymer additives. Note that almost the same results were obtained with the colored pigment obtained according to the method of Synthesis Example 2. Next, examples of the present invention will be shown. (Amounts shown are parts by weight.) Example 1 A solution of 10 g of Rhodamine B dissolved in 1 part of water was added to a solution of 100 g of montmorillonite uniformly dispersed in 5 parts of water, and the mixture was stirred at 50°C for 30 minutes. . Thereafter, 300 ml of a solution containing 0.5 g of polyvinylpyrrolidone dissolved therein was added, followed by 100 ml of 0.2 N calcium chloride, and the mixture was stirred at 50° C. for 30 minutes. The precipitate was filtered, washed with water, dried, and pulverized to obtain a colored pigment. The resulting pigment was incorporated into nail enamel. Nitrocellulose (1/2 second) 10.0 Alkyd resin 10.0 Acetyl tributyl citrate 5.0 Ethyl acetate 20.0 Butyl acetate 15.0 Ethyl alcohol 5.0 Toluene 35.0 Color pigment Appropriate amount Suspension inhibitor Example 2 100 g of Laponite CP was uniformly dispersed in 5 water. A solution prepared by dissolving 20 g of Rhodamine B in 1 was added thereto, and the mixture was stirred at 50°C for 30 minutes. Next, 100 ml of 0.2N aluminum chloride was added, and then 100 ml of a solution containing 0.5 g of carboxymethylcellulose sodium salt was added, and 50 ml of aluminum chloride was added.
C. and stirred for 30 minutes. A pigment was obtained in the same manner as in Example 1. The resulting pigment was blended into lipstick. Carnauba wax 16.0 Ozokerite 16.0 Lanolin 24.0 Liquid paraffin 24.0 Butyl stearate 10.0 Color pigment 6.0 Titanium oxide 4.0 Fragrance Appropriate amount Antioxidant

【図面の簡単な説明】[Brief explanation of the drawing]

第1図は、本発明に用いられる着色顔料及び比
較の着色顔料の着色力を示す図である。
FIG. 1 is a diagram showing the tinting strength of the colored pigment used in the present invention and a comparative colored pigment.

Claims (1)

【特許請求の範囲】[Claims] 1 カオチン交換能を有する粘土鉱物に、ローダ
ミンBと多価金属イオンと水溶性高分子を吸着さ
せて得られる、色相を黄味に調整した赤色系着色
顔料を配合したことを特徴とする化粧料。
1. A cosmetic containing a red colored pigment whose hue is adjusted to yellow, which is obtained by adsorbing Rhodamine B, polyvalent metal ions, and water-soluble polymers to clay minerals having cation exchange ability. .
JP498980A 1980-01-19 1980-01-19 Cosmetic material Granted JPS56103105A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP498980A JPS56103105A (en) 1980-01-19 1980-01-19 Cosmetic material

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP498980A JPS56103105A (en) 1980-01-19 1980-01-19 Cosmetic material

Publications (2)

Publication Number Publication Date
JPS56103105A JPS56103105A (en) 1981-08-18
JPS6248642B2 true JPS6248642B2 (en) 1987-10-15

Family

ID=11599009

Family Applications (1)

Application Number Title Priority Date Filing Date
JP498980A Granted JPS56103105A (en) 1980-01-19 1980-01-19 Cosmetic material

Country Status (1)

Country Link
JP (1) JPS56103105A (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR101026589B1 (en) 2003-01-08 2011-04-04 가부시키가이샤 시세이도 Powder having water-swelling clay mineral laminated thereon, dye-water-swelling clay mi composite and composition comprising them

Also Published As

Publication number Publication date
JPS56103105A (en) 1981-08-18

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