JPS6249247B2 - - Google Patents

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Publication number
JPS6249247B2
JPS6249247B2 JP21979084A JP21979084A JPS6249247B2 JP S6249247 B2 JPS6249247 B2 JP S6249247B2 JP 21979084 A JP21979084 A JP 21979084A JP 21979084 A JP21979084 A JP 21979084A JP S6249247 B2 JPS6249247 B2 JP S6249247B2
Authority
JP
Japan
Prior art keywords
powder
comparative example
iron oxide
mixed
pigments
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
JP21979084A
Other languages
Japanese (ja)
Other versions
JPS61100508A (en
Inventor
Kazuhisa Oono
Shigenori Kumagai
Masahisa Tsujita
Fukuji Suzuki
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 JP21979084A priority Critical patent/JPS61100508A/en
Publication of JPS61100508A publication Critical patent/JPS61100508A/en
Publication of JPS6249247B2 publication Critical patent/JPS6249247B2/ja
Granted legal-status Critical Current

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Classifications

    • 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
    • A61K8/19Cosmetics or similar toiletry preparations characterised by the composition containing inorganic ingredients
    • 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

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)
  • Chemical & Material Sciences (AREA)
  • Inorganic Chemistry (AREA)
  • Birds (AREA)
  • Epidemiology (AREA)
  • Cosmetics (AREA)

Description

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

[産業上の利用分野] 本発明は窒化硼素粉末を配合してなる使用性、
仕上がり、化粧もち、安定性および成型性が良好
な化粧料に関する。 [従来の技術] 従来の化粧料の体質顔料としてはタルク、カオ
リン、マイカ、二酸化チタン、亜鉛華、樹脂粉末
等が使用されている。これらは化粧料ののび、つ
き、カバー力、成型性等を勘案し配合量を決定し
ている。しかしながら、従来の原料を用いた化粧
料では使用性、仕上がり、化粧もち、安定性、成
型性等の点ですべてが必ずしも満足できるもので
はなかつた。すなわち、従来使用されていた化粧
品用体質顔料の概念では、艶をだすためには鱗片
状のマイカやパール剤が使用されているが、これ
らを配合すると成型性が悪くなるという欠点があ
つた。また、滑沢性を良くするために、ある程度
粒径の大きい粉末が使用されるが、これを配合す
るとザラつきを感じるようになり、また球状樹脂
粉末のナイロンパウダーやポリエチレンパウダー
なども用いられているが、これを使用すると成型
性が悪くなるという欠点があつた。さらにカバー
力、密着感を出すために二酸化チタンや亜鉛華を
配合するが、のびが悪くなるという欠点があつ
た。またマイカ、タルク、カオリンは触媒活性が
あるため、香料、オイルの劣化をひきおこし、変
臭の原因になることがわかつている。 [発明が解決しようとする問題点] 本発明者らは、こうした事情に鑑み、化粧料の
使用性、仕上がり、成型性等について鋭意研究を
重ねた結果、窒化硼素粉末を配合した化粧料はの
びが良く、密着性が良好で、なめらかで、カバー
力があり、艶がありかつ成型性が良く、さらに香
料、オイルに対する劣化作用の少ない優れた性質
を持つ化粧料であることを見出し、この知見にも
とずいて本発明を完成するに至つた。 [問題点を解決するための手段] すなわち、本発明は窒化硼素粉末を配合するこ
とを特徴とする化粧料である。 以下、本発明の構成について詳述する。 本発明で用いる窒化硼素(BN)粉末は、h−
BN、w−BN、c−BN、r−BN、t−BNなどが
ある。(科学技術庁無機材質研究所編:窒化硼素
に関する研究[無機材料研究所研究報告書第27
号]、1981.) その中ではh−BNが最も優れた性質を示す。 窒化硼素粉末の平均粒径は特に限定されないが
球状換算平均粒径(島津遠心沈降式粒度分布測定
装置SA−CP2で測定)で0.1〜30μが好ましい。
0.1μより細かいと滑沢性が損なわれ、30μ以上
ではザラツキを感じる。窒化硼素粉末は本発明の
化粧料中、0.1〜99重量%程度配合される。0.1重
量%未満では上記した効果が十分に得られず好ま
しくない。本発明の化粧料には上記した必須成分
の他に通常化粧料に用いられる他の成分を必要に
応じて適宜配合することができる。例えばタル
ク、カオリン、セリサイト、白雲母、合成雲母、
金雲母、紅雲母、黒雲母、リチア雲母、バーミキ
ユライト、炭酸マグネシウム、炭酸カルシウム、
珪ソウ土、ケイ酸マグネシウム、ケイ酸カルシウ
ム、ケイ酸アルミニウム、ケイ酸バリウム、ケイ
酸ストロンチウム、タングステン酸金属塩、シリ
カ、ヒドロキシアパタイト、硫酸バリウム、セラ
ミツクスパウダー等の無機粉末、ナイロンパウダ
ー、ポリエチレンパウダー、ベンゾグアナミンパ
ウダー、四弗化エチレンパウダー、ジスチレンベ
ンゼンピンホールポリマーパウダー、微結晶性セ
ルロース等の有機粉体、酸化チタン、酸化亜鉛等
の無機白色顔料、酸化鉄(ベンガラ)、チタン酸
鉄等の無機赤色系顔料、γ−酸化鉄等の無機褐色
系顔料、黄酸化鉄、黄土等の無機黄色系顔料、黒
酸化鉄、カーボンブラツク等の無機黒色系顔料、
マンゴバイオレツト、コバルトバイオレツト等の
無機紫色系顔料、酸化クロム、水酸化クロム、チ
タン酸コバルト等の無機緑色系顔料、群青、紺青
等の無機青色系顔料、酸化チタンコーテツド雲
母、酸化チタンコーテツドオキシ塩化ビスマス、
オキシ塩化ビスマス、酸化チタンコーテツドタル
ク、魚鱗箔、着色酸化チタンコーテツド雲母等の
パール顔料、アルミニウムパウダー、カツパーパ
ウダー等の金属粉末顔料、赤色104号、黄色4
号、黄色5号、緑色3号、青色1号、青色2号、
赤色202号、赤色226号、赤色227号、赤色230号、
橙色206号、橙色207号、黄色202号、緑色201号、
緑色204号、青色201号、緑色205号等のタール色
素、カルミン酸、ラツカイン酸、カルサミン、ブ
ラジリン、クロシン等の天然色素をレーキ化した
もの、スクワラン、流動パラフイン、ワセリン、
マイクロクリスタリンワツクス、オゾケライト、
セレシン、ミリスチン酸、パルミチン酸、ステア
リン酸、オレインイソステアリン酸、セチルアル
コール、ヘキサデシルアルコール、オレイルアル
コール、セチル2−エチルヘキサノエート、2−
エチルヘキシルパルミテート、2−オクチルドデ
シルミリステート、2−オクチルドデシルガムエ
ステル、ネオペンチルグリコール−2−エチルヘ
キサネート、イソオクチル酸トリグリセライド、
2−オクチルドデシルオレエート、イソプロピル
ミリステート、イソステアリン酸トリグリセライ
ド、ヤシ油脂肪酸トリグリセライド、オリーブ
油、アボガド油、ミツロウ、ミリスチルミリステ
ート、ミンク油、ラノリン等の各種炭化水素、高
級脂肪酸、油脂類、エステル類、高級アルコー
ル、ロウ類等の油分、アセトン、トルエン、酢酸
ブチル、酢酸エチル等の有機溶剤、アルキツド樹
脂、尿素樹脂等の樹脂、カンフア、クエン酸アセ
チルトリブチル等の可塑剤、紫外線吸収剤、酸化
防止剤、防腐剤、界面活性剤、保湿剤、香料、
水、アルコール、増粘剤等があげられる。 [発明の効果] 本発明の窒化硼素粉末を配合した化粧料は、今
まで相反する事象とされていた、カバー力があり
ながらのびが良くかつ密着感があるという現象を
実現することができ、のびが良く、艶が有り、密
着性が良好でなめらかに仕上がり、カバー力があ
り香料、オイルに対する劣化作用が小さくかつ粉
末製品の場合には成型性が良い化粧料を具現化す
ることができた。 [実施例] 次に実施例をあげて本発明を更に詳細に説明す
る。本発明はこれにより限定されるものではな
い。配合量は重量%である。 実施例に先だち評価方法を説明する。 (評価方法) 専門パネル10名により1〜5の5段階の官能評
価を下記のそれぞれの項目ごとに行つた。 のび、カバー力、密着感、つや、はがれ、なじみ 1……悪い 2……やや悪い 3……普通 4……やや良い 5……良い もち(塗布してから2時間後に判定した。) 1……化粧くずれがひどい 2……化粧くずれしている 3……やや化粧くずれしている 4……ほとんど化粧くずれしていない 5……全く化粧くずれしていない ぼかし易さ 1……非常にぼかしにくい 2……ぼかしにくい 3……普通 4……ぼかし易い 5……非常にぼかし易い 肌のきれいさ(仕上がりの化粧肌で判定した。) 1……非常にきたない 2……きたない 3……普通 4……きれい 5……非常にきれい 結果は10名の5段階評価の平均値で下記のよう
に表した。 ◎……4.5〜5.0 〇……3.5〜4.4 △……2.5〜3.4 ×……1.5〜2.4 ××……1.0〜1.4 実施例 1 油性スチツクフアンデーシヨン (1) 二酸化チタン 13 (2) カオリン 12 (3) h−BN(8μ) 13.7 (4) 赤色酸化鉄 1 (5) 黄色酸化鉄 0.7 (6) 黒色酸化鉄 0.1 (7) スクワラン 37 (8) セチル2−エチルヘキサノエート 16 (9) ソルビタンセスキオレート 1 (10) アリストワツクス 4 (11) カルナバロウ 1.3 (12) 香 料 0.2 (製法) (7)(8)と(9)を80℃で混合し、これに(1)(2)(3)(4)(5)

(6)を添加し、デイスパーで混合した後、TKミル
処理する。(10)と(11)を加熱溶解し、添加混合後、脱
気する。(12)をゆるやかに混合した後、80℃で容器
に充填し、冷却することによりスチツクフアンデ
ーシヨンを得た。 比較例 1 実施例1の処方中、h−BNをタルクに置換し
たものを実施例1と同様の方法により試作した。 実施例1と比較例1の官能評価結果を表1に示
す。
[Industrial Application Field] The present invention provides ease of use by blending boron nitride powder,
This invention relates to cosmetics with good finish, long-lasting makeup, stability, and moldability. [Prior Art] Talc, kaolin, mica, titanium dioxide, zinc white, resin powder, etc. are used as extender pigments in conventional cosmetics. The amount of these ingredients to be added is determined by taking into consideration the spreadability, adhesion, covering power, moldability, etc. of the cosmetic. However, cosmetics using conventional raw materials are not always satisfactory in terms of ease of use, finish, makeup retention, stability, moldability, etc. In other words, the conventional concept of extender pigments for cosmetics uses scaly mica and pearl agents to create luster, but when these are blended, moldability deteriorates, which is a drawback. In addition, to improve the lubricity, a powder with a somewhat large particle size is used, but when this is mixed, it feels rough, and spherical resin powders such as nylon powder and polyethylene powder are also used. However, its use had the disadvantage of poor moldability. Furthermore, titanium dioxide and zinc white are added to provide coverage and adhesion, but they have the disadvantage of being difficult to spread. Additionally, mica, talc, and kaolin have catalytic activity and are known to cause deterioration of fragrances and oils, causing odor. [Problems to be Solved by the Invention] In view of these circumstances, the present inventors have conducted intensive research on the usability, finish, moldability, etc. of cosmetics, and have found that cosmetics containing boron nitride powder can be spread easily. We discovered that this cosmetic product has excellent properties such as good adhesion, smooth coverage, gloss, and moldability, and has little deteriorating effect on fragrances and oils. Based on this, the present invention was completed. [Means for Solving the Problems] That is, the present invention is a cosmetic characterized by incorporating boron nitride powder. Hereinafter, the configuration of the present invention will be explained in detail. The boron nitride (BN) powder used in the present invention is h-
Examples include BN, w-BN, c-BN, r-BN, and t-BN. (edited by the Institute of Inorganic Materials, Science and Technology Agency: Research on boron nitride [Inorganic Materials Research Institute Research Report No. 27)
], 1981.) Among them, h-BN shows the best properties. The average particle size of the boron nitride powder is not particularly limited, but it is preferably 0.1 to 30μ in terms of spherical equivalent particle size (measured with a Shimadzu centrifugal sedimentation type particle size distribution analyzer SA-CP2).
If it is finer than 0.1μ, the smoothness will be impaired, and if it is 30μ or more, it will feel rough. Boron nitride powder is blended in the cosmetic composition of the present invention in an amount of about 0.1 to 99% by weight. If it is less than 0.1% by weight, the above-mentioned effects cannot be sufficiently obtained, which is not preferable. In addition to the above-mentioned essential ingredients, other ingredients commonly used in cosmetics can be appropriately blended into the cosmetic of the present invention as required. For example, talc, kaolin, sericite, muscovite, synthetic mica,
Phlogopite, red mica, biotite, lithian mica, vermiculite, magnesium carbonate, calcium carbonate,
Inorganic powders such as diatomaceous earth, magnesium silicate, calcium silicate, aluminum silicate, barium silicate, strontium silicate, tungstate metal salts, silica, hydroxyapatite, barium sulfate, ceramic powder, nylon powder, polyethylene powder, Organic powders such as benzoguanamine powder, tetrafluoroethylene powder, distyrene benzene pinhole polymer powder, microcrystalline cellulose, inorganic white pigments such as titanium oxide and zinc oxide, and inorganic materials such as iron oxide (red iron oxide) and iron titanate. Red pigments, inorganic brown pigments such as γ-iron oxide, inorganic yellow pigments such as yellow iron oxide and loess, inorganic black pigments such as black iron oxide and carbon black,
Inorganic purple pigments such as mango violet and cobalt violet, inorganic green pigments such as chromium oxide, chromium hydroxide, and cobalt titanate, inorganic blue pigments such as ultramarine and deep blue, titanium oxide coated mica, titanium oxide coated bismuth oxychloride,
Pearl pigments such as bismuth oxychloride, titanium oxide coated talc, fish scale foil, colored titanium oxide coated mica, metal powder pigments such as aluminum powder and cut pearl powder, Red No. 104, Yellow 4
No., Yellow No. 5, Green No. 3, Blue No. 1, Blue No. 2,
Red No. 202, Red No. 226, Red No. 227, Red No. 230,
Orange No. 206, Orange No. 207, Yellow No. 202, Green No. 201,
Tar pigments such as Green No. 204, Blue No. 201, and Green No. 205, lakes of natural pigments such as carminic acid, latukaic acid, calsamine, brasilin, and crocin, squalane, liquid paraffin, petrolatum,
Microcrystalline wax, ozokerite,
Ceresin, myristic acid, palmitic acid, stearic acid, oleic isostearic acid, cetyl alcohol, hexadecyl alcohol, oleyl alcohol, cetyl 2-ethylhexanoate, 2-
Ethylhexyl palmitate, 2-octyldodecyl myristate, 2-octyldodecyl gum ester, neopentyl glycol-2-ethylhexanate, isooctyl triglyceride,
Various hydrocarbons such as 2-octyldodecyl oleate, isopropyl myristate, isostearic acid triglyceride, coconut oil fatty acid triglyceride, olive oil, avocado oil, beeswax, myristyl myristate, mink oil, lanolin, higher fatty acids, fats and oils, esters, Oils such as higher alcohols and waxes, organic solvents such as acetone, toluene, butyl acetate, and ethyl acetate, resins such as alkyd resins and urea resins, plasticizers such as camphor and acetyltributyl citrate, ultraviolet absorbers, and antioxidants. , preservatives, surfactants, humectants, fragrances,
Examples include water, alcohol, and thickeners. [Effects of the Invention] The cosmetics containing the boron nitride powder of the present invention can achieve the phenomena of having good coverage, good adhesion, and a feeling of adhesion, which have been considered contradictory phenomena until now. We were able to create a cosmetic that spreads easily, has gloss, has good adhesion, has a smooth finish, has good coverage, has little deterioration effect on fragrances and oils, and has good moldability in the case of powder products. . [Example] Next, the present invention will be explained in more detail by giving examples. The present invention is not limited thereby. The blending amount is in weight%. An evaluation method will be explained prior to examples. (Evaluation method) A sensory evaluation of 1 to 5 was performed on each of the following items by a panel of 10 experts. Spreadability, coverage, adhesion, luster, peeling, blending 1...Poor 2...Slightly poor 3...Average 4...Slightly good 5...Good stickiness (Judged 2 hours after application.) 1... ...Makeup is badly discolored 2...Makeup is discolored 3...Makeup is slightly discolored 4...Makeup is almost not discolored 5...Makeup is not discolored at all Ease of blurring 1...Very difficult to blur 2...Difficult to blur 3...Normal 4...Easy to blur 5...Cleanliness of the skin that is very easy to blur (judged based on the finished makeup skin) 1...Very dirty 2...Dirty 3... Fair 4...Beautiful 5...Very beautiful The results are the average of 10 people's five-point ratings and are expressed as follows. ◎...4.5-5.0 〇...3.5-4.4 △...2.5-3.4 ×...1.5-2.4 ××...1.0-1.4 Example 1 Oil-based stick foundation (1) Titanium dioxide 13 (2) Kaolin 12 (3) h-BN (8μ) 13.7 (4) Red iron oxide 1 (5) Yellow iron oxide 0.7 (6) Black iron oxide 0.1 (7) Squalane 37 (8) Cetyl 2-ethylhexanoate 16 (9) ) Sorbitan sesquiolate 1 (10) Aristovax 4 (11) Carnauba wax 1.3 (12) Fragrance 0.2 (Production method) Mix (7)(8) and (9) at 80℃, and add (1)(2) to this. )(3)(4)(5)
and
Add (6), mix with a disper, and then process with a TK mill. (10) and (11) are heated and dissolved, added and mixed, and then degassed. After gently mixing (12), the mixture was filled into a container at 80°C and cooled to obtain a stick foundation. Comparative Example 1 A sample was prepared in the same manner as in Example 1 except that h-BN was replaced with talc in the formulation of Example 1. Table 1 shows the sensory evaluation results of Example 1 and Comparative Example 1.

【表】 表1から明らかなように本発明に係るスチツク
フアンデーシヨンは官能評価項目のいずれにおい
ても優れていることがわかる。 実施例 2 アイシヤドー (1) タルク 6 (2) 白雲母 5 (3) h−BN(5μ) 70 (4) 群 青 8 (5) 黄色酸化鉄 3 (6) 黒色酸化鉄 1 (7) スクワラン 4 (8) セチル2−エチルヘキサノエート 1.9 (9) ソルビタンセスキオレート 0.8 (10) 防腐剤 0.1 (11) 香 料 0.2 (製法) (1)(2)(3)(4)(5)と(6)をヘンシエルミキサーで混合
し、これに(7)(8)(9)(10)と(11)を加熱溶解混合したも

を吹き付け、混合した後粉砕し、中皿に成型しア
イシヤドーを得た。 比較例 2 実施例2の処方中、h−BNを白雲母に置換し
たものを実施例2と同様の方法により試作した。 実施例2と比較例2の官能評価結果を表2に示
す。
[Table] As is clear from Table 1, the stick foundation according to the present invention is excellent in all sensory evaluation items. Example 2 Eyeshadow (1) Talc 6 (2) Muscovite 5 (3) h-BN (5μ) 70 (4) Group Blue 8 (5) Yellow iron oxide 3 (6) Black iron oxide 1 (7) Squalane 4 (8) Cetyl 2-ethylhexanoate 1.9 (9) Sorbitan sesquiolate 0.8 (10) Preservative 0.1 (11) Flavoring 0.2 (Production method) (1)(2)(3)(4)(5) and ( Mix 6) with a Henschel mixer, spray a heated and melted mixture of (7), (8), (9), (10) and (11) on this, mix, crush, and form into a medium plate to make eye shadow. Obtained. Comparative Example 2 A sample was produced in the same manner as in Example 2 except that h-BN in the formulation of Example 2 was replaced with muscovite. Table 2 shows the sensory evaluation results of Example 2 and Comparative Example 2.

【表】 表2から明らかなように本発明に係るアイシヤ
ドーは比較例に比べ優れていることがわかる。さ
らに2×3cmの中皿に100Kg/cm2の圧力で成型し
た場合の硬度[オルゼン式カタサ試験機(JIS
K6301)(1ポンド荷重)により測定]は実施例
2が21、比較例2が56で本発明の実施例2の方が
成型性が良いことがわかる。 実施例 3 ブラツシヤー (1) タルク 12.6 (2) 絹雲母 8.1 (3) h−BN(5μ) 60.9 (4) r−BN(15μ) 3 (5) t−BN(10μ) 3 (6) 群 青 0.1 (7) 黄色酸化鉄 0.1 (8) 赤色酸化鉄 0.4 (9) 赤色226号 0.4 (10) チタンマイカ 3 (11) スクワラン 3 (12) 2−エチルヘキシルパルミテート 5 (13) 防腐剤 0.3 (14) 香 料 0.1 (製法) (1)(2)(3)(4)(5)(6)(7)(8)と(9)をヘンシエルミキサ
ーで
混合し、これに(11)(12)(13)と(14)を加熱溶解混
合したものを吹き付け、混合した後粉砕し、さら
に(10)を加え混合した後、中皿に成型しブラツシヤ
ーを得た。 比較例 3 実施例3の処方中、60.9重量%のh−BN(5
μ)と3重量%のr−BN(15μ)と3重量%の
t−BN(10μ)とを絹雲母に置換したものを実
施例3と同様の方法により試作した。実施例3と
比較例3の官能評価結果を表3に示す。
[Table] As is clear from Table 2, the eye shadow according to the present invention is superior to the comparative example. Furthermore, the hardness when molded into a 2 x 3 cm medium plate at a pressure of 100 kg/cm 2 [Olzen type Katasa tester (JIS
K6301) (1 pound load)] was 21 for Example 2 and 56 for Comparative Example 2, indicating that Example 2 of the present invention had better moldability. Example 3 Blusher (1) Talc 12.6 (2) Sericite 8.1 (3) h-BN (5μ) 60.9 (4) r-BN (15μ) 3 (5) t-BN (10μ) 3 (6) Group Blue 0.1 (7) Yellow iron oxide 0.1 (8) Red iron oxide 0.4 (9) Red No. 226 0.4 (10) Titanium mica 3 (11) Squalane 3 (12) 2-ethylhexyl palmitate 5 (13) Preservative 0.3 (14) ) Fragrance 0.1 (Production method) (1)(2)(3)(4)(5)(6)(7)(8) and (9) are mixed in a Hensiel mixer, and (11)(12 )(13) and (14) were heated and mixed and sprayed, mixed and crushed, further (10) was added and mixed, and then molded into a medium plate to obtain a brush. Comparative Example 3 In the formulation of Example 3, 60.9% by weight of h-BN (5
A sample was produced in the same manner as in Example 3, in which sericite was substituted with 3% by weight of r-BN (15μ) and 3% by weight of t-BN (10μ). Table 3 shows the sensory evaluation results of Example 3 and Comparative Example 3.

【表】 表3から明らかなように本発明に係るブラツシ
ヤーは官能評価項目のいずれにおいても優れてい
ることがわかる。さらに4×6cmの中皿に120
Kg/cm2の圧力で成型した場合の硬度は実施例3が
22、比較例3が35で本発明の実施例3の方が成型
性が良いことがわかる。 実施例 4 パウダーフアンデーシヨン (1) 酸化チタン 2 (2) タルク 10 (3) 白雲母 3 (4) h−BN(5μ) 55 (5) h−BN(10μ) 5 (6) ナイロンパウダー 12 (7) 赤色酸化鉄 0.5 (8) 黄色酸化鉄 1 (9) 黒色酸化鉄 0.1 (10) シリコンオイル 1 (11) 2−エチルヘキシルパルミテート 9 (12) ソルビタンセスキオレート 1 (13) 防腐剤 0.3 (14) 香 料 0.1 (製法) (1)〜(8)と(9)をヘンシエルミキサーで混合し、こ
れに(10)(11)(12)(13)と(14)を加熱溶解混合したも
のを添加混合後粉砕し、これを中皿に成型しパウ
ダーフアンデーシヨンを得た。 比較例 4 実施例4の処方中、55重量%のh−BN(5
μ)と5重量%のh−BN(10μ)とを4重量%
の酸化チタン、50重量%の絹雲母、6重量%のタ
ルクに置換したものを実施例4と同様の方法によ
り試作した。 実施例4と比較例4の官能評価結果を表4に示
す。
[Table] As is clear from Table 3, the blusher according to the present invention is excellent in all sensory evaluation items. 120 more on a 4x6cm medium plate
The hardness of Example 3 when molded at a pressure of Kg/ cm2 is
22 and Comparative Example 3 was 35, indicating that Example 3 of the present invention had better moldability. Example 4 Powder foundation (1) Titanium oxide 2 (2) Talc 10 (3) Muscovite 3 (4) h-BN (5μ) 55 (5) h-BN (10μ) 5 (6) Nylon powder 12 (7) Red iron oxide 0.5 (8) Yellow iron oxide 1 (9) Black iron oxide 0.1 (10) Silicone oil 1 (11) 2-ethylhexyl palmitate 9 (12) Sorbitan sesquiolate 1 (13) Preservative 0.3 ( 14) Fragrance 0.1 (Production method) (1) to (8) and (9) were mixed in a Henschel mixer, and (10), (11), (12), (13) and (14) were heated and mixed. After addition and mixing, the mixture was pulverized and molded into a medium plate to obtain a powder foundation. Comparative Example 4 In the formulation of Example 4, 55% by weight of h-BN (5% by weight)
μ) and 5% by weight of h-BN (10μ) at 4% by weight.
A trial production was made in the same manner as in Example 4, except that titanium oxide, 50% by weight of sericite, and 6% by weight of talc were substituted. Table 4 shows the sensory evaluation results of Example 4 and Comparative Example 4.

【表】 表4に示される如く本発明の実施例4のほうが
高い評価を受けていることがわかる。 さらに直径5.3cmの中皿で160Kg/cm2の圧力で成
型した場合の硬度は実施例4が29、比較例4が46
で本発明の実施例4の方が成型性が良いことがわ
かる。 実施例 5 乳化フアンデーシヨン (1) ステアリン酸 0.4 (2) イソステアリン酸 0.3 (3) セチル2−エチルヘキサノエート 4 (4) 流動パラフイン 11 (5) POE(10)ステアリルエーテル 2 (6) タルク 15 (7) 顔 料 4 (8) セチルアルコール 0.3 (9) 防腐剤 0.07 (10) h−BN(1μ) 3 (11) トリエタノールアミン 0.42 (12) プロピレングリコール 5 (13) 防腐剤 0.02 (14) イオン交換水 54.19 (15) 香 料 0.3 (製法) (1)(2)(3)(4)(5)(6)(7)(8)と(9)を85℃に加熱溶解混
合し
た後、(10)を添加し均一に分散する。これに(11)(12)
(13)と(14)を85℃に加熱溶解混合した混合物
を徐々に添加し乳化する。乳化時温度を10分間保
持して撹拌した後、撹拌冷却して45℃とする。こ
れに(15)を加え35℃まで撹拌冷却を続け、取り
出し、容器に充填して乳化フアンデーシヨンを得
た。 比較例 5 実施例5の処方中、h−BNを亜鉛華に置換し
たものを実施例5と同様の方法により試作した。 実施例5と比較例5の官能評価結果を表5に示
す。
[Table] As shown in Table 4, it can be seen that Example 4 of the present invention received higher evaluations. Furthermore, when molded with a medium plate of 5.3 cm in diameter at a pressure of 160 kg/cm 2 , the hardness of Example 4 was 29 and that of Comparative Example 4 was 46.
It can be seen that Example 4 of the present invention has better moldability. Example 5 Emulsified foundation (1) Stearic acid 0.4 (2) Isostearic acid 0.3 (3) Cetyl 2-ethylhexanoate 4 (4) Liquid paraffin 11 (5) POE (10) Stearyl ether 2 (6) Talc 15 (7) Pigment 4 (8) Cetyl alcohol 0.3 (9) Preservative 0.07 (10) h-BN (1μ) 3 (11) Triethanolamine 0.42 (12) Propylene glycol 5 (13) Preservative 0.02 (14) ) Ion exchange water 54.19 (15) Fragrance 0.3 (Production method) (1)(2)(3)(4)(5)(6)(7)(8) and (9) were heated and mixed at 85℃. After that, (10) is added and dispersed uniformly. To this (11)(12)
A mixture of (13) and (14) heated and mixed at 85°C is gradually added and emulsified. After stirring while maintaining the temperature during emulsification for 10 minutes, the mixture is stirred and cooled to 45°C. (15) was added thereto, continued stirring and cooling to 35°C, taken out, and filled into a container to obtain an emulsified foundation. Comparative Example 5 A sample was produced in the same manner as in Example 5 except that h-BN in the formulation of Example 5 was replaced with zinc white. Table 5 shows the sensory evaluation results of Example 5 and Comparative Example 5.

【表】 表5から明らかなように本発明に係る乳化フア
ンデーシヨンは比較例に比べ優れていることがわ
かる。 実施例 6 化粧下地 (1) イオン交換水 68.164 (2) グリセリン 7 (3) プロピレングリコール 7 (4) ヘキサメチレン酸ナトリウム 0.01 (5) EDTA・3Na2水塩 0.01 (6) 赤色酸化鉄 0.01 (7) 黄色酸化鉄 0.001 (8) 黒色酸化鉄 0.005 (9) 二酸化チタン(アナターゼ) 1 (10) h−BN(5μ) 1 (11) カセイソーダ 0.2 (12) スクワラン 3 (13) セチル2−エチルヘキサノエート 3 (14) ワセリン 1 (15) セトステアリルアルコール 3 (16) ステアリン酸 2 (17) グリセリルモノステアレート 2 (18) POE(10)ステアリルエーテル 1 (19) パラベン 0.5 (20) 香 料 0.1 (製法) 1〜(11)までの原料を70℃で混合、これに(12)〜
(20)までの原料を混合溶解したものを添加し混
合乳化した後脱気、冷却、濾過した後容器に充填
し化粧下地を得た。 比較例 6 実施例6の処方中h−BNをタルクに置換した
ものを実施例6と同様な方法により試作した。実
施例6と比較例6の官能評価の結果を表6に示
す。
[Table] As is clear from Table 5, the emulsified foundation according to the present invention is superior to the comparative example. Example 6 Makeup base (1) Ion exchange water 68.164 (2) Glycerin 7 (3) Propylene glycol 7 (4) Sodium hexamethyleneate 0.01 (5) EDTA・3Na dihydrate 0.01 (6) Red iron oxide 0.01 (7) Yellow iron oxide 0.001 (8) Black iron oxide 0.005 (9) Titanium dioxide (anatase) 1 (10) h-BN (5μ) 1 (11) Caustic soda 0.2 (12) Squalane 3 (13) Cetyl 2-ethylhexanoate 3 (14) Vaseline 1 (15) Cetostearyl alcohol 3 (16) Stearic acid 2 (17) Glyceryl monostearate 2 (18) POE (10) Stearyl ether 1 (19) Paraben 0.5 (20) Fragrance 0.1 (Manufacturing method ) Mix raw materials from 1 to (11) at 70℃, and add (12) to this.
A mixed and dissolved mixture of the raw materials up to (20) was added, mixed and emulsified, deaerated, cooled, filtered, and then filled into a container to obtain a makeup base. Comparative Example 6 A sample was produced in the same manner as in Example 6 except that h-BN in the formulation of Example 6 was replaced with talc. Table 6 shows the results of the sensory evaluation of Example 6 and Comparative Example 6.

【表】 表6から明らかなように本発明に係る化粧下地
は官能評価項目のいずれにおいても優れているこ
とがわかる。 実施例 7 ネイルエナメル (1) ニトロセルロース 12 (2) 変性アルキツド樹脂 12 (3) クエン酸アセチルトリブチル 5 (4) 酢酸n−ブチル 36.4 (5) 酢酸エチル 6 (6) n−ブチルアルコール 2 (7) トルエン 21 (8) 酸化鉄顔料 0.5 (9) 二酸化チタン 0.1 (10) パール顔料 2 (11) h−BZ(1μ) 2 (12) 有機変性モンモリロナイト 1 (製法) (1)(2)(3)(4)の一部、(5)(6)と(7)を溶解しこれに(12
)と
(4)の残部をゲル状にしたものを添加混合し、さら
に(8)(9)(10)と(11)を添加混合し、容器に充填しネイル
エナメルを得た。 比較例 7 実施例7の処方中h−BNをパール顔料に置換
したものを実施例7と同様の方法により試作し
た。実施例7と比較例7の官能評価の結果を表7
に示す。
[Table] As is clear from Table 6, the makeup base according to the present invention is excellent in all sensory evaluation items. Example 7 Nail enamel (1) Nitrocellulose 12 (2) Modified alkyd resin 12 (3) Acetyl tributyl citrate 5 (4) N-Butyl acetate 36.4 (5) Ethyl acetate 6 (6) N-Butyl alcohol 2 (7) ) Toluene 21 (8) Iron oxide pigment 0.5 (9) Titanium dioxide 0.1 (10) Pearl pigment 2 (11) h-BZ (1μ) 2 (12) Organically modified montmorillonite 1 (Production method) (1)(2)(3 )(4), (5)(6) and (7) are dissolved and (12
)and
The remainder of (4) in gel form was added and mixed, and (8), (9), (10) and (11) were further added and mixed, and the mixture was filled into a container to obtain nail enamel. Comparative Example 7 A sample was produced in the same manner as in Example 7 except that h-BN in the formulation of Example 7 was replaced with a pearl pigment. Table 7 shows the results of the sensory evaluation of Example 7 and Comparative Example 7.
Shown below.

【表】 表7から明らかなように本発明に係るネイルエ
ナメルは官能評価項目のいずれにおいても優れて
いることがわかる。特にハガレの強さは特筆すべ
きところである。さらにパール顔料に比べてh−
BNは比重が小さく沈降しにくいので増粘剤の量
を少なくできるという利点がある。 実施例 8 アイライナー (1) 黒色酸化鉄 7 (2) 二酸化チタン 5 (3) h−BN(0.5μ) 2 (4) 酢酸ビニル樹脂エマルジヨン 45 (5) グリセリン 6 (6) POE(20)ソルビタンモノラウレート 1.8 (7) カルボキシメチルセルロース(10%水溶液)
18 (8) ビーガム(5%水分散液) 5 (9) イオン交換水 9.9 (10) 防腐剤 0.1 (11) 香 料 0.2 (製法) (9)に(5)(6)を加え、これに(1)〜(3)を添加し、コロ
イドミル処理する(顔料部)。他の成分を混合
し、70℃で顔料部を加えて均一に分散した後、冷
却、充填しアイライナーを得た。 比較例 8 実施例8の処方中h−BNをカオリンに置換し
たものを実施例8と同様な方法により試作した。
実施例8と比較例8を官能評価したところ、描き
やすくもちが良いという結果が得られた。 実施例 9 口 紅 (1) 炭化水素ワツクス 3 (2) キヤンデリラワツクス 1 (3) グリセリルイソステアレート 40 (4) 流動パラフイン 45.8 (5) 二酸化チタン 4 (6) H−BN(3μ) 3 (7) 有機顔料 3 (8) 香 料 0.2 (製法) (1)(2)(3)と(4)を85℃に加熱溶解し、これに(5)(6)と
(7)を加え撹拌混合した後(8)を撹拌混合し、容器に
充填して口紅を得た。 比較例 9 実施例9の処方中h−BNをパール顔料に置換
したものを実施例9と同様な方法により試作し
た。実施例9と比較例9を官能評価したところ、
のび、密着感、つや、もちが良く、さらに口紅を
くり出す時のハガレ現象がなく離型性が良く収縮
も少なかつた。 実施例 10 フアンシーパウダー (1) h−BN(5μ) 95 (2) w−BN(4μ) 4 (3) 香 料 1 (4) 酸化鉄顔料 適量 (製法) (1)(2)と(4)を混合した後(3)を加え混合し容器に充
填してフアンシーパウダーを得た。 比較例 10、11 実施例10の処方中95重量%のh−BN(5μ)
と4重量%のw−BN(4μ)とをタルク(比較
例10)、マイカ(比較例11)に置換したものを実
施例10と同様な方法により試作した。実施例10と
比較例10、11を37℃恒温槽に1ケ月保存したサン
プルと、各々のコントロール(同処方で製造した
フアンシーパウダーの製造直後)とを比較した。 (評価方法) 官能評価により匂い安定性について判定した。 ◎……コントロールと殆ど変わらない △……コントロールと比べて変臭している ×……コントロールと比べてかなり変臭している 表8に官能評価結果を示す。
[Table] As is clear from Table 7, the nail enamel according to the present invention is excellent in all sensory evaluation items. In particular, the strength of peeling is noteworthy. Furthermore, compared to pearl pigments, h-
BN has a small specific gravity and is difficult to settle, so it has the advantage that the amount of thickener can be reduced. Example 8 Eyeliner (1) Black iron oxide 7 (2) Titanium dioxide 5 (3) h-BN (0.5μ) 2 (4) Vinyl acetate resin emulsion 45 (5) Glycerin 6 (6) POE (20) Sorbitan Monolaurate 1.8 (7) Carboxymethyl cellulose (10% aqueous solution)
18 (8) Veegum (5% water dispersion) 5 (9) Ion exchange water 9.9 (10) Preservative 0.1 (11) Flavor 0.2 (Production method) Add (5) and (6) to (9) and add to this Add (1) to (3) and perform colloid mill treatment (pigment part). The other ingredients were mixed, a pigment part was added at 70°C, and the mixture was uniformly dispersed, then cooled and filled to obtain an eyeliner. Comparative Example 8 A sample was produced in the same manner as in Example 8 except that h-BN in the formulation of Example 8 was replaced with kaolin.
When Example 8 and Comparative Example 8 were subjected to sensory evaluation, results were obtained that they were easy to draw and had good hold. Example 9 Lipstick (1) Hydrocarbon wax 3 (2) Candelilla wax 1 (3) Glyceryl isostearate 40 (4) Liquid paraffin 45.8 (5) Titanium dioxide 4 (6) H-BN (3μ) 3 (7) Organic pigment 3 (8) Fragrance 0.2 (Production method) Heat and dissolve (1)(2)(3) and (4) at 85℃, and add (5)(6) to this.
After (7) was added and mixed with stirring, (8) was mixed with stirring and filled into a container to obtain a lipstick. Comparative Example 9 A sample was produced in the same manner as in Example 9 except that h-BN in the formulation of Example 9 was replaced with a pearl pigment. A sensory evaluation of Example 9 and Comparative Example 9 revealed that
The lipstick had good spreadability, adhesion, gloss, and longevity, and there was no peeling phenomenon when the lipstick was applied, and the mold release was good and there was little shrinkage. Example 10 Fancy powder (1) h-BN (5μ) 95 (2) w-BN (4μ) 4 (3) Fragrance 1 (4) Iron oxide pigment Appropriate amount (manufacturing method) (1) (2) and ( After mixing 4), (3) was added and mixed, and the mixture was filled into a container to obtain fancy powder. Comparative Examples 10, 11 95% by weight h-BN (5μ) in the formulation of Example 10
Samples were produced in the same manner as in Example 10, except that 4% by weight of w-BN (4μ) was replaced with talc (Comparative Example 10) and mica (Comparative Example 11). Samples of Example 10 and Comparative Examples 10 and 11 stored in a 37°C constant temperature bath for one month were compared with each control (immediately after production of Fancy Powder produced using the same formulation). (Evaluation method) Odor stability was determined by sensory evaluation. ◎...Almost no difference from the control △...Odor has changed compared to the control ×...Odor has changed considerably compared to the control Table 8 shows the sensory evaluation results.

【表】 表8から明らかなように実施例10は高い評価を
受けていることがわかる。
[Table] As is clear from Table 8, Example 10 was highly evaluated.

Claims (1)

【特許請求の範囲】[Claims] 1 窒化硼素粉末を配合することを特徴とする化
粧料。
1. A cosmetic characterized by containing boron nitride powder.
JP21979084A 1984-10-19 1984-10-19 Cosmetic Granted JPS61100508A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP21979084A JPS61100508A (en) 1984-10-19 1984-10-19 Cosmetic

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP21979084A JPS61100508A (en) 1984-10-19 1984-10-19 Cosmetic

Publications (2)

Publication Number Publication Date
JPS61100508A JPS61100508A (en) 1986-05-19
JPS6249247B2 true JPS6249247B2 (en) 1987-10-19

Family

ID=16741058

Family Applications (1)

Application Number Title Priority Date Filing Date
JP21979084A Granted JPS61100508A (en) 1984-10-19 1984-10-19 Cosmetic

Country Status (1)

Country Link
JP (1) JPS61100508A (en)

Cited By (1)

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JPH0764704B2 (en) * 1986-07-29 1995-07-12 株式会社資生堂 Cosmetics
JPS6396110A (en) * 1986-10-14 1988-04-27 Sekisui Plastics Co Ltd cosmetics
JPH01106806A (en) * 1987-10-20 1989-04-24 Kenichi Kawasaki Promoter for reduction of stain following melanin chromatosis occurring on human skin
JPH0510156U (en) * 1991-07-18 1993-02-09 光洋精工株式会社 Expansion and contraction cover mounting structure for the rack and pinion type steering device
JPH05279594A (en) * 1992-02-07 1993-10-26 Merck Patent Gmbh Platelet-like pigment
CA2105005A1 (en) * 1992-09-10 1994-03-11 Marianne Elliott Color cosmetic composition
JPH11302126A (en) * 1998-04-24 1999-11-02 Kose Corp Liquid eye liner cosmetic
JP2003104842A (en) * 2001-09-28 2003-04-09 Kose Corp Aqueous solid cosmetic
JP2003104841A (en) * 2001-09-28 2003-04-09 Kose Corp Oily solid cosmetic
JP2007084478A (en) * 2005-09-21 2007-04-05 Tayca Corp Cosmetics
JP5430149B2 (en) 2006-04-17 2014-02-26 三菱鉛筆株式会社 Aqueous liquid makeup cosmetics
US9040094B2 (en) 2007-02-13 2015-05-26 Sakai Chemical Industry Co., Ltd. Flaky particle and cosmetic
US20120171136A1 (en) * 2009-06-30 2012-07-05 Shiseido Company, Ltd. Pressed Powder Cosmetic Composition
JP5758142B2 (en) * 2011-02-14 2015-08-05 花王株式会社 Cosmetics
JP6085475B2 (en) * 2012-12-28 2017-02-22 花王株式会社 Solid powder cosmetic
JP6412406B2 (en) * 2014-10-30 2018-10-24 花王株式会社 Water-in-oil emulsified cosmetic

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2008099467A1 (en) 2007-02-13 2008-08-21 Sakai Chemical Industry Co., Ltd. Flaky particle and cosmetic
EP2540670A1 (en) 2007-02-13 2013-01-02 Sakai Chemical Industry Co., Ltd. Flaky particles coated with a fatty acid metal salt, process for preparing said flaky particles and cosmetic comprising the same

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