JPS6137711A - Cosmetic - Google Patents
CosmeticInfo
- Publication number
- JPS6137711A JPS6137711A JP16113484A JP16113484A JPS6137711A JP S6137711 A JPS6137711 A JP S6137711A JP 16113484 A JP16113484 A JP 16113484A JP 16113484 A JP16113484 A JP 16113484A JP S6137711 A JPS6137711 A JP S6137711A
- Authority
- JP
- Japan
- Prior art keywords
- zinc oxide
- powder
- cosmetic
- oxide powder
- fine
- 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
Links
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q17/00—Barrier preparations; Preparations brought into direct contact with the skin for affording protection against external influences, e.g. sunlight, X-rays or other harmful rays, corrosive materials, bacteria or insect stings
- A61Q17/04—Topical preparations for affording protection against sunlight or other radiation; Topical sun tanning preparations
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/19—Cosmetics or similar toiletry preparations characterised by the composition containing inorganic ingredients
- A61K8/27—Zinc; Compounds thereof
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B82—NANOTECHNOLOGY
- B82Y—SPECIFIC USES OR APPLICATIONS OF NANOSTRUCTURES; MEASUREMENT OR ANALYSIS OF NANOSTRUCTURES; MANUFACTURE OR TREATMENT OF NANOSTRUCTURES
- B82Y5/00—Nanobiotechnology or nanomedicine, e.g. protein engineering or drug delivery
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
- A61K2800/40—Chemical, physico-chemical or functional or structural properties of particular ingredients
- A61K2800/41—Particular ingredients further characterized by their size
- A61K2800/413—Nanosized, i.e. having sizes below 100 nm
Abstract
Description
【発明の詳細な説明】
[産業上の利用分野]
本発明は化粧料、さらに詳しくは微粒子酸化亜鉛粉末を
系中に含有してなる、分散安定性良好で、皮膚に塗布し
たときに透明感を有しているので白っぽくならず、かつ
紫外線防止効果を有し、消炎・殺菌効果をも併せもつ優
れた化粧料に関する。Detailed Description of the Invention [Industrial Field of Application] The present invention relates to a cosmetic, more specifically, a cosmetic containing fine-particle zinc oxide powder, which has good dispersion stability and has a transparent appearance when applied to the skin. The present invention relates to an excellent cosmetic that does not become whitish due to its properties, has an ultraviolet ray prevention effect, and also has anti-inflammatory and sterilizing effects.
[従来の技術]
従来、化粧料に配合される粉末は一般的には粒径0.5
μ程度のものであり、最も粒径の小さいものでも300
〜400人程度の酸化チタンが知られているのみであっ
た(特公昭47−42502号公報)。[Prior Art] Conventionally, powders blended into cosmetics generally have a particle size of 0.5.
The smallest particle size is about 300 μm.
Only about 400 titanium oxides were known (Japanese Patent Publication No. 47-42502).
[発明が解決しようとする問題点]
配合粉末の粒径が上記の通り 300〜400人程度以
上であると、皮膚に塗布した場合にはどうしても白っぽ
さが目立ち、不自然な感じになることは否めない。この
ため、紫外線防止効果を付与したり肌にさっばり感を与
えたすせんがために化粧料中に粉末を配合しようとする
ときにも、この白っぼさが大いに障害となっていた。[Problems to be Solved by the Invention] If the particle size of the blended powder is about 300 to 400 or more as described above, when applied to the skin, whitishness will be noticeable and it will look unnatural. That is undeniable. For this reason, this whitishness has been a major hindrance when trying to incorporate powder into cosmetics to provide UV protection or give a refreshing feel to the skin.
本発明者らはこうした現状にかんがみ、酸化亜鉛に着目
し鋭意検討した結果、このものを微粒子化して化粧料基
剤中に配合すれば、上記欠点を解決しうろことを見いだ
し、もって本発明をなすに至ったのである。In view of the current situation, the inventors of the present invention focused on zinc oxide and, as a result of intensive study, discovered that the above-mentioned drawbacks could be solved by making this material into fine particles and blending it into a cosmetic base.Thus, the present invention has been achieved. That's what happened.
[問題点を解決するための手段]
すなわち、本発明は微粒子酸化亜鉛粉末を含有すること
を特徴とする化粧料である。[Means for Solving the Problems] That is, the present invention is a cosmetic characterized by containing fine-particle zinc oxide powder.
以下、本発明の構成について詳述する。Hereinafter, the configuration of the present invention will be explained in detail.
本発明で用いる微粒子酸化亜鉛粉末は粒径10〜200
人の微粒子酸化亜鉛粉末であり、機械的粉砕などによっ
ても得ることができるが、製造の容易さ、得られた微粒
子粉末の化粧料基剤中への分散性の良さ、粒径の均一な
ことから、水溶液中で調整した硫酸亜鉛もしくは塩化亜
鉛のヒドロゾル中のコロイド粒子を陰イオン界面活性剤
で親油的に転換したのち、有機溶媒にてフラッシングし
、ついで該有機溶媒を乾燥除去して得られる微粒子酸化
亜鉛粉末がとくに好ましい。上記コロイドゾル(以下、
ゾル法という)を経て得られる微粒子酸化亜鉛粉末の粒
径は10〜200人の範囲、一般的には50〜100人
の範囲に存する。The fine particle zinc oxide powder used in the present invention has a particle size of 10 to 200.
It is human microparticle zinc oxide powder, which can also be obtained by mechanical grinding, etc., but it is easy to manufacture, has good dispersibility of the obtained microparticle powder in cosmetic bases, and has a uniform particle size. The colloidal particles in the hydrosol of zinc sulfate or zinc chloride prepared in an aqueous solution are converted to lipophilic form with an anionic surfactant, then flushed with an organic solvent, and then the organic solvent is removed by drying. Particularly preferred are finely divided zinc oxide powders. The above colloid sol (hereinafter,
The particle size of the fine-particle zinc oxide powder obtained through the sol method is in the range of 10 to 200 particles, generally in the range of 50 to 100 particles.
ゾル法についてさらに詳しく説明する。The sol method will be explained in more detail.
この方法においては、まず、塩化亜鉛もしくは硫酸亜鉛
水溶液中に炭酸ナトリウム水溶液を添加してヒドロゾル
を形成する。塩化亜鉛もしくは硫酸亜鉛水溶液の濃度は
0.1〜1.0モル程度、炭酸ナトリウム水溶液の濃度
は0.2〜1.0モル程度、塩化亜鉛もしくは硫酸亜鉛
水溶液:炭酸ナトリウム水溶液の比率は重量比で1:1
程度である。In this method, first, an aqueous sodium carbonate solution is added to an aqueous solution of zinc chloride or zinc sulfate to form a hydrosol. The concentration of zinc chloride or zinc sulfate aqueous solution is about 0.1 to 1.0 mol, the concentration of sodium carbonate aqueous solution is about 0.2 to 1.0 mol, and the ratio of zinc chloride or zinc sulfate aqueous solution: sodium carbonate aqueous solution is by weight 1:1
That's about it.
つぎに、陰イオン界面活性剤を加えて該ヒドロゾルを親
油化する。用いられる陰イオン界面活性剤はアルキルベ
ンゼンスルフォン酸ナトリウム凡ラウリル硫酸ナトリウ
ム、ラウリル硫酸カリウム、アルキル硫酸トリエタノー
ルアミンエーテル、ロート油、ジアルキルスルフオサク
シネートナトリウム、ジ2エチルへキシルスルフオサク
シネートナトリウム、ラウリルポリエチレングリコール
スルフオサクシネートナトリウム、アルキルエーテルサ
ルフェートナトリウム、ポリオキシエチレン(以下、
POEという)アルキル硫酸ナトリウム、N−バルミト
イルアスパラギン酸ジトリエタノールアミン、ヤシ油脂
肪酸メチルタウリドナトリウム、ミリストイルメチルタ
ウリンナトリウム、ラウリルメチルタウリドナトリウム
、ラウロイルグルタミン酸ナトリウム、酸化ヤシ油脂肪
酸グリセリン硫酸ナトリウム、ステアロイルグルタミン
酸ジナトリウム、ミリストイルグルタミン酸ナトリウム
、POEアルキルフェニルエーテル硫酸ナトリウム、
POEアルキル硫酸トリエタノールアミン、ラウロイル
ザルコシンナトリウム、カゼインナトリウム、パルミチ
ン酸ナトリウム、ラウリン酸ナトリウム、POE硬化硬
化ヒマシシマレイン酸エステルであるが、とくにアルキ
ルベンゼンスルフオン酸ナトリウム、ラウリル硫酸ナト
リウム、ラウリル硫酸カリウム、アルキル硫酸トリエタ
ノールアミンエーテルが好ましい。陰イオン界面活性剤
の添加量は塩化亜鉛もしくは硫酸亜鉛と炭酸ナトリウム
との量比によっても異なるが、おおむね塩化亜鉛もしく
は硫酸亜鉛1モルに対して0.05〜0.15iルの範
囲で選択すれば良い。Next, an anionic surfactant is added to make the hydrosol lipophilic. The anionic surfactants used are sodium alkylbenzenesulfonate, sodium lauryl sulfate, potassium lauryl sulfate, triethanolamine ether alkyl sulfate, funnel oil, sodium dialkyl sulfosuccinate, sodium di-ethylhexyl sulfosuccinate, and sodium lauryl sulfate. Sodium polyethylene glycol sulfosuccinate, sodium alkyl ether sulfate, polyoxyethylene (hereinafter referred to as
POE) sodium alkyl sulfate, N-balmitoyl aspartate ditriethanolamine, sodium coconut oil fatty acid methyltauride, sodium myristoylmethyltaurate, sodium lauryl methyltauride, sodium lauroyl glutamate, sodium oxidized coconut oil fatty acid glycerol sulfate, stearoyl Disodium glutamate, sodium myristoyl glutamate, POE sodium alkyl phenyl ether sulfate,
POE alkyl sulfate triethanolamine, sodium lauroyl sarcosine, sodium caseinate, sodium palmitate, sodium laurate, POE cured castor shimaleate, especially sodium alkylbenzene sulfonate, sodium lauryl sulfate, potassium lauryl sulfate, Alkyl sulfate triethanolamine ethers are preferred. The amount of anionic surfactant added varies depending on the ratio of zinc chloride or zinc sulfate to sodium carbonate, but it is generally selected within the range of 0.05 to 0.15 l per mol of zinc chloride or zinc sulfate. Good.
本発明に係るゾル法にあっては、上記陰イオン界面活性
剤の親水性・親油性のバランスなどを適宜選択すること
により、得られる微粒子酸化亜鉛粉末を親水性にも親油
性にも調整することができる。たとえば、微粒子酸化亜
鉛粉末を水性基剤の化粧料中に配合しようとするときに
は陰イオン界面活性剤としてラウリル硫酸ナトリウム、
ラウリル硫酸カリウム、アルキル硫酸トリエタノールア
ミンエーテルなどを用いると親水性の微粒子酸化亜鉛粉
末が得られる。また、陰イオン界面活性剤としてアルキ
ルベンゼンスルフオン酸ナトリウムなどを用いると親油
性の微粒子酸化亜鉛粉末が得られるので油性基剤の化粧
料に配合するのに好適である。In the sol method according to the present invention, by appropriately selecting the balance between hydrophilicity and lipophilicity of the anionic surfactant, the obtained fine particle zinc oxide powder is adjusted to be either hydrophilic or lipophilic. be able to. For example, when blending fine-particle zinc oxide powder into aqueous-based cosmetics, sodium lauryl sulfate is used as an anionic surfactant.
Hydrophilic fine particle zinc oxide powder can be obtained by using potassium lauryl sulfate, alkyl sulfate triethanolamine ether, etc. Furthermore, when sodium alkylbenzenesulfonate or the like is used as an anionic surfactant, lipophilic fine particle zinc oxide powder can be obtained, which is suitable for blending into oil-based cosmetics.
親油化された該ヒドロゾルは、次に有機溶媒でフラッシ
ングされる。用いられる有機溶媒は上記陰イオン界面活
性剤を溶解するものであれば何でもよい。たとえば、キ
シレン、トルエン、ペンゼンなどやこれらの混合溶媒が
用いられる。有機溶媒の量はヒドロゾル溶液に対して重
量比で0.5〜1.0倍量程度の範囲で選択される。The lipophilized hydrosol is then flushed with an organic solvent. Any organic solvent may be used as long as it dissolves the anionic surfactant. For example, xylene, toluene, penzene, or a mixed solvent thereof is used. The amount of the organic solvent is selected within a range of about 0.5 to 1.0 times the weight ratio of the hydrosol solution.
こうして得られたオルガノゾルは乾燥して微粒子酸化亜
鉛粉末を分取する。乾燥方法はとくに制限はなく、常法
に従えば良い。The organosol thus obtained is dried to separate fine particles of zinc oxide powder. There are no particular restrictions on the drying method, and any conventional method may be used.
本発明にあっては、微粒子酸化亜鉛粉末は化粧料全量中
の0.−5〜100重量%、紫外線防止効果の面からは
10重量%以上、肌にさっばりした効果をあたえる観点
からは50重量%以上配合されることが好ましい。In the present invention, the fine particle zinc oxide powder is 0.0% of the total amount of the cosmetic. -5 to 100% by weight, preferably 10% by weight or more from the viewpoint of UV protection effect, and 50% by weight or more from the viewpoint of giving a refreshing effect to the skin.
本発明の微粒子酸化亜鉛粉末を含有してなる化粧料の剤
型は任意であり、広く粉末系、可溶化系、乳化系、粉末
分散可溶化系、粉末分散乳化系、粉末分散油系などをと
ることができる。The dosage form of the cosmetic containing the fine-particle zinc oxide powder of the present invention is arbitrary, and broadly includes powder-based, solubilized-based, emulsified-based, powder-dispersed-solubilized, powder-dispersed-emulsified, powder-dispersed oil-based, etc. You can take it.
用途も任意であり、化粧水、乳液、クリーム、化粧油な
どのフェーシャル化粧料をはじめ、ファンデーション、
パウダー、口紅、頬紅、アイシャドーなどのノーキャン
プ化粧料などの広範な化粧料に用いることができる。Applications are arbitrary, including facial cosmetics such as lotions, emulsions, creams, and cosmetic oils, as well as foundations,
It can be used in a wide range of cosmetics, including non-camping cosmetics such as powder, lipstick, blush, and eye shadow.
[発明の効果]
本発明に係る微粒子酸化亜鉛粉末含有化粧料は、良好な
透明感を有しているので肌に塗布したときの白っぽさも
なくかつ紫外線防止効果に優れ、肌にさっばりとした使
用感を与え、また化粧料基剤中での分散安定性も良好で
ある。さらに、粉末であるがために液状の紫外線吸収剤
のような肌に対する刺激、アレルギーなどの心配もない
。安全性良好な化粧料である。[Effects of the Invention] The cosmetic containing fine-particle zinc oxide powder according to the present invention has good transparency, so when applied to the skin, there is no whitish appearance, and it has an excellent UV protection effect, leaving a light feeling on the skin. It gives a pleasant feel when used, and also has good dispersion stability in cosmetic bases. Furthermore, since it is a powder, there is no need to worry about skin irritation or allergies, which is the case with liquid UV absorbers. It is a cosmetic with good safety.
[実施例コ
次に、本発明の微粒子酸化亜鉛粉末の製造例および微粒
子酸化亜鉛粉末を化粧料中に配合した実施例を示す。本
発明はこれにより限定されるものではない。[Example 2] Next, an example of manufacturing a fine-particle zinc oxide powder of the present invention and an example in which the fine-particle zinc oxide powder was blended into a cosmetic will be shown. The present invention is not limited thereby.
製造例1
1M塩化亜鉛水溶液中に0.1M炭酸ナトリウム水溶液
を1:1の重量比で添加する。添加速度は25d/+n
in、の割合とした。30分間攪拌を続は白色のヒドロ
ゾルを得たのち、アルキルベンゼンスルフオン酸ナトリ
ウムを0.15M加えてゾルを親油化し、ついでキシレ
ンを254加えてフラッシングし、白色のオルガノゾル
を得た。このものを減圧下で乾燥してキシレンを留去し
て粒径70〜100人の微粒子酸化亜鉛粉末1gを得た
。この微粒子酸化亜鉛粉末は親油性であり、油性化粧料
への配合に適する。Production Example 1 A 0.1M aqueous sodium carbonate solution is added to a 1M aqueous zinc chloride solution at a weight ratio of 1:1. Addition rate is 25d/+n
The ratio was set as in. After stirring for 30 minutes, a white hydrosol was obtained. 0.15 M of sodium alkylbenzenesulfonate was added to make the sol lipophilic, and then 254 ml of xylene was added for flushing to obtain a white organosol. This product was dried under reduced pressure and xylene was distilled off to obtain 1 g of fine particle zinc oxide powder having a particle size of 70 to 100 particles. This fine-particle zinc oxide powder is lipophilic and suitable for blending into oil-based cosmetics.
製造例2
製造例1のアルキルベンゼンスルフオン酸ナトリウムを
ラウリル硫酸ナトリウムに置換した他は製造例1と同様
に製造して親水性の微粒子酸化亜鉛粉末を得た。このも
のは水性化粧料への配合に適する。Production Example 2 Hydrophilic fine-particle zinc oxide powder was obtained in the same manner as Production Example 1 except that sodium alkylbenzenesulfonate in Production Example 1 was replaced with sodium lauryl sulfate. This product is suitable for blending into aqueous cosmetics.
実施例1 (化粧水)
■グリセリン 3.0重量%■プロピ
レングリコール 2.0■オレイルアルコール
0.1■POE(20)ソルビタン
モノラウリン酸エステル 2.0
■エタノール 10.0■香料
0.1■染料
通量
■微粒子酸化亜鉛粉末
(製造例゛2で得たもの)1.0
■水 残部
■に■■を加え溶解する(水相部)。■に■■■■■を
溶解する(エタノール部)。水相部にエタノール部を加
えて可溶化し、化粧水を得た。得られた化粧水はさっば
りした使用感を持ち、肌に塗布したときの白フぼさもな
くて透明感も良好でありながら紫外線防止効果を有し、
また、肌の消炎効果にも優れていた。さらに、微粒子酸
化亜鉛粉末の粒径が細かいためにとくに増粘剤などを加
えなくとも分散性は良好であった。Example 1 (lotion) ■ Glycerin 3.0% by weight ■ Propylene glycol 2.0 ■ Oleyl alcohol
0.1 ■ POE (20) Sorbitan monolaurate 2.0 ■ Ethanol 10.0 ■ Fragrance
0.1 ■ Dye
Volume ■Fine particle zinc oxide powder (obtained in Production Example 2) 1.0 ■Water Add ■■ to the remaining ■ and dissolve (aqueous phase). Dissolve ■■■■■ in ■ (ethanol part). An ethanol portion was added to the aqueous phase for solubilization to obtain a lotion. The resulting lotion has a light feel, does not leave a white flaky appearance when applied to the skin, has good transparency, and has UV protection effects.
It also had excellent anti-inflammatory effects on the skin. Furthermore, because the particle size of the fine zinc oxide powder was small, the dispersibility was good even without adding a thickener or the like.
実施例2 (日焼は止めクリーム)
■ステアリン酸 10.0重量%■ステ
アリルアルコール 4.0■ステアリン酸ブチル
6.0■モノステアリン酸グリセリン
(自己乳化型)2.0
■香料 適量
■プロピレングリコール 10.0■グリセリン
3.0■水酸化カリウム
0.4■微粒子酸化亜鉛粉末
(製造例2で得たもの)4.0
[相]水 残部[相]に■■
■■を加え溶解して70℃に保つ(水相部)。■■■■
■を溶解して70℃に保つ(油相部)。Example 2 (Sunscreen cream) ■Stearic acid 10.0% by weight ■Stearyl alcohol 4.0 ■Butyl stearate 6.0 ■Glyceryl monostearate (self-emulsifying type) 2.0 ■Fragrance appropriate amount ■Propylene glycol 10.0 ■ Glycerin
3.0 ■ Potassium hydroxide
0.4 ■ Fine particle zinc oxide powder (obtained in Production Example 2) 4.0 [Phase] Water The remainder [Phase] ■■
Add ■■ and dissolve and keep at 70°C (aqueous phase). ■■■■
Dissolve (1) and keep at 70°C (oil phase).
水相部に油相部を加えて乳化し、冷却してクリームを得
た。得られたクリームはとくに紫外線防止効果に優れて
いた。The oil phase was added to the water phase, emulsified, and cooled to obtain cream. The resulting cream had particularly excellent UV protection effects.
実施例3(日焼は止め乳液)
■ステアリン酸 2.0重量%■セタノ
ール 1.5■ワセリン
3.0■流動パラフイン 8
.0■POE(10)モノオレイン酸
エステル 2.0
■香料 適量
■グリセリン 2.0■プロピレング
リコール 5.0■トリエタノールアミン
1.0[相]微粒子酸化亜鉛粉末
(製造例2で得たもの)5.5
■水 残部
■に■■■[相]を加え熔解して70℃に保つ(水相部
)。■■■■■■を溶解して70℃に保つ(油相部)。Example 3 (Sunscreen lotion) ■Stearic acid 2.0% by weight■Cetanol 1.5■Vaseline
3.0■Liquid paraffin 8
.. 0 ■ POE (10) monooleic acid ester 2.0 ■ Fragrance appropriate amount ■ Glycerin 2.0 ■ Propylene glycol 5.0 ■ Triethanolamine
1.0 [Phase] Fine particle zinc oxide powder (obtained in Production Example 2) 5.5 ■Water ■■■ [Phase] is added to the remaining ■ and melted and kept at 70°C (water phase). ■■■■■■ is dissolved and kept at 70°C (oil phase).
水相部に油相部を加えて乳化し、冷却して乳液を得た。The oil phase was added to the water phase, emulsified, and cooled to obtain a milky lotion.
得られた乳液はとくに紫外線防止効果に優れており、ま
た使用感もさっばりしたものであワたO
実施例4(ファンデーシリン)
■ステアリン酸 2.8重量%■モノス
テアリン酸
プロピレングリコール 2.8
■モノステアリン酸グリセリン
(自己乳化型)2.8
0流動パラフイン 24.6■トリエタノー
ルアミン 1.4■プロピレングリコール
15.0■微粒子酸化亜鉛粉末
(製造例1で得たもの)6.0
■酸化鉄赤 1.5■酸化鉄黄
2.5[相]香料
適量■防腐剤 適量
@水 残部
@に■■■を加え溶解して70℃に保つ(水相部)■■
■■[相]■を溶解してこれに■■■を分散して70℃
に保つ(油相部)。水相部に油相部を加えて乳化し、冷
却してファンデーションを得た。The obtained emulsion has particularly excellent UV protection effects and has a light feel upon use.Example 4 (Foundation Silin) ■Stearic acid 2.8% by weight ■Propylene glycol monostearate 2. 8 ■ Glyceryl monostearate (self-emulsifying type) 2.8 0 Liquid paraffin 24.6 ■ Triethanolamine 1.4 ■ Propylene glycol
15.0 ■ Fine particle zinc oxide powder (obtained in Production Example 1) 6.0 ■ Iron oxide red 1.5 ■ Iron oxide yellow
2.5 [Phase] Fragrance
Appropriate amount ■ Preservative Appropriate amount @ water Add ■■■ to the remaining @ and dissolve and keep at 70℃ (water phase) ■■
■■ [Phase] Dissolve ■■ and disperse ■■■ in it at 70°C.
(oil phase). The oil phase was added to the water phase, emulsified, and cooled to obtain a foundation.
実施例5(白粉)
■タルク 10.2重量%■酸
化チタン 1.0■カオリン
10.0■微粒子酸化亜鉛粉末
(製造例1で得たもの”) 77.0■酸化鉄赤
黄黒 1.8■酸化鉄黄
2.5■香料 適量
上記成分を混合して白粉を得た。このものは肌に塗布し
たときに透明感が良好で白っぽくならず、化粧抑え効果
にもすぐれていた。また、紫外線防止効果も充分であっ
た。Example 5 (white powder) ■Talc 10.2% by weight■Titanium oxide 1.0■Kaolin
10.0 ■ Fine particle zinc oxide powder (obtained in Production Example 1) 77.0 ■ Iron oxide red yellow black 1.8 ■ Iron oxide yellow
2.5 ■Fragrance A white powder was obtained by mixing appropriate amounts of the above components. When applied to the skin, this product had good transparency, did not appear whitish, and had an excellent makeup-reducing effect. In addition, the UV protection effect was sufficient.
Claims (4)
化粧料。(1) A cosmetic characterized by containing fine-particle zinc oxide powder.
る特許請求の範囲第(1)項記載の化粧料。(2) The cosmetic according to claim (1), wherein the fine particle zinc oxide powder has a particle size of 10 to 200 Å.
る特許請求の範囲第(1)項記載の化粧料。(3) The cosmetic according to claim (1), wherein the fine particle zinc oxide powder has a particle size of 50 to 100 Å.
鉛もしくは塩化亜鉛のヒドロゾル中のコロイド粒子を陰
イオン界面活性剤で親油的に転換したのち、有機溶媒に
てフラッシングし、ついで該有機溶媒を乾燥除去して得
られる微粒子酸化亜鉛粉末である特許請求の範囲第(1
)項ないし第(3)項のいずれかに記載の化粧料。(4) Fine-particle zinc oxide powder is prepared in an aqueous solution by converting colloidal particles in a hydrosol of zinc sulfate or zinc chloride into lipophilic form with an anionic surfactant, then flushing with an organic solvent, and then flushing with an organic solvent. Claim No. 1, which is a fine particle zinc oxide powder obtained by drying and removing
Cosmetics according to any one of paragraphs ) to (3).
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP16113484A JPS6137711A (en) | 1984-07-31 | 1984-07-31 | Cosmetic |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP16113484A JPS6137711A (en) | 1984-07-31 | 1984-07-31 | Cosmetic |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS6137711A true JPS6137711A (en) | 1986-02-22 |
JPH0577644B2 JPH0577644B2 (en) | 1993-10-27 |
Family
ID=15729241
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP16113484A Granted JPS6137711A (en) | 1984-07-31 | 1984-07-31 | Cosmetic |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS6137711A (en) |
Cited By (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6284017A (en) * | 1985-10-08 | 1987-04-17 | Okamura Seiyu Kk | Cosmetic composition and production thereof |
JPS62198608A (en) * | 1986-02-25 | 1987-09-02 | Sumitomo Cement Co Ltd | Cosmetic |
JPS63132821A (en) * | 1986-11-21 | 1988-06-04 | Shiseido Co Ltd | Anti-suntan cosmetic |
JPH069363A (en) * | 1992-06-29 | 1994-01-18 | Fuiru Internatl:Kk | Medicinal cosmetic |
CH684387A5 (en) * | 1993-04-22 | 1994-09-15 | Greiter Ag | Cosmetic or pharmaceutical product for topical application to the skin and the mucous membranes |
US5366660A (en) * | 1991-10-04 | 1994-11-22 | Tioxide Specialties Limited | Dispersions |
US5573753A (en) * | 1991-10-04 | 1996-11-12 | Tioxide Specialties Limited | Method of preparing sunscreens |
EP0786982A4 (en) * | 1993-04-28 | 1997-08-06 | ||
US5663213A (en) * | 1994-02-28 | 1997-09-02 | Rohm And Haas Company | Method of improving ultraviolet radiation absorption of a composition |
WO2001013874A1 (en) * | 1999-08-19 | 2001-03-01 | Shiseido Co., Ltd. | Cosmetic sunscreen preparation |
JP2001058934A (en) * | 1999-08-19 | 2001-03-06 | Shiseido Co Ltd | Antisuntan cosmetic |
JP2008248043A (en) * | 2007-03-29 | 2008-10-16 | Naris Cosmetics Co Ltd | Allergen inactivator and allergen inactivating product comprising the same |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP4569597B2 (en) * | 2007-04-26 | 2010-10-27 | 堺化学工業株式会社 | Zinc oxide production method and zinc oxide |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS57120514A (en) * | 1981-01-20 | 1982-07-27 | Pola Chem Ind Inc | Cosmetic having ultraviolet light shielding effect |
JPS57205319A (en) * | 1981-06-15 | 1982-12-16 | Mitsubishi Metal Corp | Manufacture of very fine zinc oxide powder |
JPS57209824A (en) * | 1981-06-16 | 1982-12-23 | Mitsubishi Metal Corp | Preparation of skin-colored fine zinc oxide powder |
JPS5962517A (en) * | 1982-10-04 | 1984-04-10 | Shiseido Co Ltd | Anti-suntan cosmetic |
JPS60231607A (en) * | 1984-04-28 | 1985-11-18 | Kobayashi Kooc:Kk | Antisuntan cosmetic |
-
1984
- 1984-07-31 JP JP16113484A patent/JPS6137711A/en active Granted
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS57120514A (en) * | 1981-01-20 | 1982-07-27 | Pola Chem Ind Inc | Cosmetic having ultraviolet light shielding effect |
JPS57205319A (en) * | 1981-06-15 | 1982-12-16 | Mitsubishi Metal Corp | Manufacture of very fine zinc oxide powder |
JPS57209824A (en) * | 1981-06-16 | 1982-12-23 | Mitsubishi Metal Corp | Preparation of skin-colored fine zinc oxide powder |
JPS5962517A (en) * | 1982-10-04 | 1984-04-10 | Shiseido Co Ltd | Anti-suntan cosmetic |
JPS60231607A (en) * | 1984-04-28 | 1985-11-18 | Kobayashi Kooc:Kk | Antisuntan cosmetic |
Cited By (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6284017A (en) * | 1985-10-08 | 1987-04-17 | Okamura Seiyu Kk | Cosmetic composition and production thereof |
JPS62198608A (en) * | 1986-02-25 | 1987-09-02 | Sumitomo Cement Co Ltd | Cosmetic |
JPS63132821A (en) * | 1986-11-21 | 1988-06-04 | Shiseido Co Ltd | Anti-suntan cosmetic |
US5573753A (en) * | 1991-10-04 | 1996-11-12 | Tioxide Specialties Limited | Method of preparing sunscreens |
US5605652A (en) * | 1991-10-04 | 1997-02-25 | Tioxide Specialties Limited | Method of preparing sunscreens |
US5366660A (en) * | 1991-10-04 | 1994-11-22 | Tioxide Specialties Limited | Dispersions |
JPH069363A (en) * | 1992-06-29 | 1994-01-18 | Fuiru Internatl:Kk | Medicinal cosmetic |
CH684387A5 (en) * | 1993-04-22 | 1994-09-15 | Greiter Ag | Cosmetic or pharmaceutical product for topical application to the skin and the mucous membranes |
EP0786982A4 (en) * | 1993-04-28 | 1997-08-06 | ||
EP0786982A1 (en) * | 1993-04-28 | 1997-08-06 | Sunsmart, Inc. | Topical ultra-violet radiation protectants |
US5663213A (en) * | 1994-02-28 | 1997-09-02 | Rohm And Haas Company | Method of improving ultraviolet radiation absorption of a composition |
WO2001013874A1 (en) * | 1999-08-19 | 2001-03-01 | Shiseido Co., Ltd. | Cosmetic sunscreen preparation |
JP2001058934A (en) * | 1999-08-19 | 2001-03-06 | Shiseido Co Ltd | Antisuntan cosmetic |
CN100369601C (en) * | 1999-08-19 | 2008-02-20 | 株式会社资生堂 | Cosmetic sunscreen prpearation |
JP2008248043A (en) * | 2007-03-29 | 2008-10-16 | Naris Cosmetics Co Ltd | Allergen inactivator and allergen inactivating product comprising the same |
Also Published As
Publication number | Publication date |
---|---|
JPH0577644B2 (en) | 1993-10-27 |
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Legal Events
Date | Code | Title | Description |
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LAPS | Cancellation because of no payment of annual fees |