JPH0216725B2 - - Google Patents

Info

Publication number
JPH0216725B2
JPH0216725B2 JP58175708A JP17570883A JPH0216725B2 JP H0216725 B2 JPH0216725 B2 JP H0216725B2 JP 58175708 A JP58175708 A JP 58175708A JP 17570883 A JP17570883 A JP 17570883A JP H0216725 B2 JPH0216725 B2 JP H0216725B2
Authority
JP
Japan
Prior art keywords
lysine
powder
skin
oil
cosmetic
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 - Lifetime
Application number
JP58175708A
Other languages
Japanese (ja)
Other versions
JPS6067406A (en
Inventor
Kenjiro Meguro
Koichiro Sagawa
Hiroshi Yokota
Masahiro Takehara
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.)
Ajinomoto Co Inc
Original Assignee
Ajinomoto Co Inc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Ajinomoto Co Inc filed Critical Ajinomoto Co Inc
Priority to JP17570883A priority Critical patent/JPS6067406A/en
Priority to EP19840306449 priority patent/EP0139481B1/en
Priority to US06/653,024 priority patent/US4640943A/en
Priority to DE8484306449T priority patent/DE3485717D1/en
Publication of JPS6067406A publication Critical patent/JPS6067406A/en
Publication of JPH0216725B2 publication Critical patent/JPH0216725B2/ja
Granted legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09CTREATMENT OF INORGANIC MATERIALS, OTHER THAN FIBROUS FILLERS, TO ENHANCE THEIR PIGMENTING OR FILLING PROPERTIES ; PREPARATION OF CARBON BLACK  ; PREPARATION OF INORGANIC MATERIALS WHICH ARE NO SINGLE CHEMICAL COMPOUNDS AND WHICH ARE MAINLY USED AS PIGMENTS OR FILLERS
    • C09C3/00Treatment in general of inorganic materials, other than fibrous fillers, to enhance their pigmenting or filling properties
    • C09C3/08Treatment with low-molecular-weight non-polymer organic compounds
    • 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
    • A61K8/40Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
    • A61K8/44Aminocarboxylic acids or derivatives thereof, e.g. aminocarboxylic acids containing sulfur; Salts; Esters or N-acylated derivatives thereof
    • 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
    • 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
    • A61Q1/08Preparations containing skin colorants, e.g. pigments for cheeks, e.g. rouge
    • 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
    • A61Q1/10Preparations containing skin colorants, e.g. pigments for eyes, e.g. eyeliner, mascara
    • 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
    • A61Q1/12Face or body powders for grooming, adorning or absorbing
    • DTEXTILES; PAPER
    • D21PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21HPULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
    • D21H17/00Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
    • D21H17/63Inorganic compounds
    • D21H17/67Water-insoluble compounds, e.g. fillers, pigments
    • D21H17/69Water-insoluble compounds, e.g. fillers, pigments modified, e.g. by association with other compositions prior to incorporation in the pulp or paper
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01PINDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
    • C01P2004/00Particle morphology
    • C01P2004/60Particles characterised by their size
    • C01P2004/61Micrometer sized, i.e. from 1-100 micrometer
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01PINDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
    • C01P2006/00Physical properties of inorganic compounds
    • C01P2006/22Rheological behaviour as dispersion, e.g. viscosity, sedimentation stability
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01PINDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
    • C01P2006/00Physical properties of inorganic compounds
    • C01P2006/90Other properties not specified above

Landscapes

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

Description

【発明の詳細な説明】 本発明はN−アシルリジンを粉末の形態で配合
してなる化粧料に関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a cosmetic containing N-acyl lysine in powder form.

従来、化粧用粉体原料としては、二酸化チタ
ン、亜鉛華、タルク、カオリン、沈降性炭酸カル
シウム、塩基性炭酸マグネシウム等の無機粉末、
或いはナイロン12、架橋ポリスチレン等の合成高
分子からなる有機粉体が知られている。これら化
粧用粉体には、以下の特性、即ち(1)皮膚の表面を
被覆し、シミ、ソバカスをかくす、(2)皮膚に塗布
する際の伸び、滑らかさに優れる、(3)皮膚への吸
着性が良く化粧崩れが起りにくい、(4)汗、分泌物
の吸収性が良い、(5)他の化粧用基材との配合が容
易である、(6)安全性が高い、といつた特性を有す
ることが要求されている。
Conventionally, cosmetic powder raw materials include inorganic powders such as titanium dioxide, zinc white, talc, kaolin, precipitated calcium carbonate, and basic magnesium carbonate;
Alternatively, organic powders made of synthetic polymers such as nylon 12 and crosslinked polystyrene are known. These cosmetic powders have the following characteristics: (1) they cover the surface of the skin and hide spots and freckles, (2) they spread well and are smooth when applied to the skin, and (3) they are gentle on the skin. (4) Good absorption of sweat and secretions, (5) Easy to blend with other cosmetic base materials, and (6) High safety. It is required to have certain characteristics.

然るに、二酸化チタン等の無機粉体では、良好
な被覆力、使用感を有するものの親水性が高く、
油性基材との配合が困難であり、また、タルクで
は皮膚のPHHが5から6であるのに対し、著しく
そのPHHが高く表面活性も強い為、実際の使用に
あたつては、安全性の面から大きな制約を受ける
といつた欠点を有している。
However, inorganic powders such as titanium dioxide have good covering power and feel when used, but are highly hydrophilic.
It is difficult to blend with oil-based base materials, and the PHH of talc is significantly higher than that of the skin, which is 5 to 6, and has a strong surface activity. It has the disadvantage of being subject to significant restrictions in terms of

一方、香粧品分野に於ける新しい素材として最
近利用され始めた、ナイロン12、或いは架橋ポリ
スチレン等の有機粉体に於いては、微小真球状の
形態がもたらす滑り性の良さ、或いは安全性の高
さといつた長所に対し、水性基材への分散性、
汗、分泌物等の吸収性、皮膚に対する吸着性等が
悪く、化粧崩れが起り易いことが欠点として指摘
されている。
On the other hand, organic powders such as nylon 12 or cross-linked polystyrene, which have recently begun to be used as new materials in the cosmetics field, are known for their fine spherical shape, which provides good slipperiness and high safety. In contrast to the advantages mentioned above, dispersibility in aqueous base materials,
It has been pointed out that it has poor absorbency for sweat, secretions, etc. and adsorption to the skin, and that it tends to cause makeup to come off.

そこで近年、これらの粉体に適当な表面処理を
施すことによつて、上述のごとき欠点を改良せん
とする試みが種々なされている。
Therefore, in recent years, various attempts have been made to improve the above-mentioned drawbacks by subjecting these powders to appropriate surface treatments.

例えば、二酸化チタンを長鎖脂肪酸と高級アル
コールからなるモノエステルで疎水性化表面処理
し、油性基材への分散性及び安全性を向上させる
方法(特開昭53−124627)、或いはタルク表面を
ポリアミノ酸でコーテインングすることによつて
刺激性を緩和し、皮膚に対する被覆力及び吸着力
を向上させる方法(特開昭55−79315)、或いはナ
イロン12の粉体表面を二酸化チタンでコーテイン
グすることとによつて、親水性を賦与し、分散性
及び水性汚れの吸着性を向上させる方法
(COSMETICSANDTOILETRIES94(12)、33
(1979))、等がそれである。
For example, there is a method in which the surface of titanium dioxide is hydrophobized with a monoester consisting of a long-chain fatty acid and a higher alcohol to improve its dispersibility and safety in oily base materials (Japanese Patent Laid-Open No. 124627-1983), or a method in which the surface of talc is A method of alleviating irritation and improving skin coverage and adsorption power by coating with polyamino acids (Japanese Patent Application Laid-Open No. 1983-79315), or coating the surface of nylon 12 powder with titanium dioxide. A method of imparting hydrophilicity and improving dispersibility and adsorption of aqueous stains by
(1979)), etc.

しかしながら、かかる表面処理、即ち親水性粉
体の疎水化、或いは疎水性粉体の親水化という方
法を用いても、上述した化粧用粉体に要求される
特性を充分満足するものは得られておらず、しか
も表面処理に伴うコストの増加、作業性の低下、
及び常時一定した品質の粉体を製造することが困
難であるといつた問題が新たに生じているのが現
状である。
However, even if such surface treatment, i.e., making a hydrophilic powder hydrophobic or making a hydrophobic powder hydrophilic, it is not possible to obtain a powder that satisfies the above-mentioned characteristics required for cosmetic powders. Moreover, there is an increase in cost associated with surface treatment, a decrease in workability,
At present, new problems have arisen, such as the difficulty of producing powder of constant quality at all times.

本発明者らは、かかる実情に鑑み、化粧用原料
として利用し得る新規粉体素材について鋭意検討
した結果、以下の一般式で表わされるN−アシル
リジンの粉末が、各種アシルアミノ酸の中では特
異的に、水、スクワラン、流動パラフイン等の
種々の溶媒に対し難溶であり、また、膨潤もせ
ず、これら溶媒中に於いても粉体として安定した
形態を保ち、皮膚に対して温和で、しかも化粧料
原料の一成分として配合したとき、皮膚に対する
付着性、被覆力、及び分泌物吸収性の優れた化粧
料が製造出来ることを見いだし、本発明を完成し
た。
In view of the above circumstances, the present inventors have conducted intensive studies on new powder materials that can be used as cosmetic raw materials. In addition, it is poorly soluble in various solvents such as water, squalane, and liquid paraffin, does not swell, maintains a stable powder form even in these solvents, and is gentle on the skin. The present invention was completed based on the discovery that when incorporated as a component of a cosmetic raw material, a cosmetic with excellent adhesion to the skin, covering power, and absorption of secretions can be produced.

即ち、本発明は下記一般式(1)乃至(3)で表わされ
るN−アシルリジンのうち少なくとも一種を粉末
の形態で配合してなる化粧料に関するものであ
る。
That is, the present invention relates to a cosmetic containing at least one type of N-acyl lysine represented by the following general formulas (1) to (3) in powder form.

但し、一般式(1)および(2)に於いて、RCOは炭
素数8乃至22の脂肪族アシル基を示す。また、上
記一般式(3)に於いて、R′COとR″COはそれぞれ
炭素数1乃至22であつて両者の合計が9から44と
なる脂肪族アシル基を示す。) 上記一般式(3)表示のN〓−N〓−ジアシルリジン
を得るには、リジンのアルカリ水溶液中に脂肪酸
クロライドを滴下させる、いわゆる
SCHOTTENBAUMANN反応が用いられる。
この際予めα−位、或いはε−位のアミノ基を保
護しておけば、ε−位、或いはα−位のみが選択
的にアシル化された化合物(1)、(2)を得ることがで
きる。また、化合物(1)は、リジンの脂肪酸塩を
100℃から250℃の温度で加熱脱水することによつ
ても得ることができる。(特開昭51−28610)。生
成したN−アシルリジンは、ろ過等の方法により
固液分離して採取し、必要に応じ脱色、精製を行
なつた後、ボールミル、コロイドミル、アトマイ
ザー等の粉砕機を用いて所望する粒度まで粉砕
し、目的とする粉体とすることができる。
However, in general formulas (1) and (2), RCO represents an aliphatic acyl group having 8 to 22 carbon atoms. In addition, in the above general formula (3), R′CO and R″CO each represent an aliphatic acyl group having 1 to 22 carbon atoms and a total of 9 to 44.) The above general formula ( 3) To obtain the indicated N〓-N〓-diacyl lysine, fatty acid chloride is dropped into an alkaline aqueous solution of lysine, so-called
A SCHOTTENBAUMANN reaction is used.
At this time, if the amino group at the α-position or ε-position is protected in advance, compounds (1) and (2) in which only the ε-position or α-position is selectively acylated can be obtained. can. Compound (1) also contains a fatty acid salt of lysine.
It can also be obtained by heating and dehydrating at a temperature of 100°C to 250°C. (Japanese Patent Publication No. 51-28610). The generated N-acyl lysine is collected by solid-liquid separation using methods such as filtration, decolorized and purified as necessary, and then pulverized to the desired particle size using a pulverizer such as a ball mill, colloid mill, or atomizer. Then, it can be made into the desired powder.

アシル基としては、通常炭素数8から22の脂肪
族アシル基が用いられるが、その炭素数及びアシ
ル基の数を変えることによつて、N−アシルリジ
ンの親水性、疎水性、滑り性、付着力、被覆力等
を調整することが可能である。
As the acyl group, an aliphatic acyl group having 8 to 22 carbon atoms is usually used, but by changing the number of carbon atoms and the number of acyl groups, it is possible to improve the hydrophilicity, hydrophobicity, slipperiness, and adhesion of N-acyl lysine. It is possible to adjust adhesion, covering power, etc.

本発明に於けるN−アシルリジンを例示するな
らば、例えば、N〓−ヘキサノイルリジン、N〓−
オレオイルリジン、N〓−ラウロイルリジン、N〓
−ミリストイルリシジン、N〓−パルミトイルリ
ジン、N〓−ステアロイルリジン、N〓−ヘキサノ
イルリジン、N〓−オレオイルリジン、N〓−ラウ
ロイルリジン、N〓−ミリストイルリジン、N〓−
パルミトイルリジン、N〓−ステアロイルリジン、
N〓−ラウロイル−N〓−ステアロイルリジン、N〓
−ヘキサノイル−N〓−パルミトイルリジン、N〓
−N〓−ジラウロイルリジン等の他、これらの混
合物が挙げられる。尚、これらN−アシルリジン
は、光学活性体でもセラミ体でも同様に用いるこ
とが出来る。
Examples of N-acyl lysine in the present invention include N〓-hexanoyl lysine, N〓-
Oleoyl lysine, N〓−Lauroyl lysine, N〓
-Myristoyllisine, N〓-palmitoyllisine, N〓-stearoyllisine, N〓-hexanoyllisine, N〓-oleoyllysine, N〓-lauroyllysine, N〓-myristoyllisine, N〓-
Palmitoyl lysine, N-stearoyl lysine,
N〓−lauroyl−N〓−stearoyl lysine, N〓
-hexanoyl-N〓-palmitoyl lysine, N〓
In addition to -N〓-dilauroyl lysine and the like, mixtures thereof can be mentioned. Note that these N-acyl lysines can be used in the same manner as optically active forms or cerami forms.

従来より、N〓−アシルリジン又はその金属塩
が、両性界面活性剤として洗浄剤(特開昭50−
97605)、或いはポリ塩化ビニル等ハロゲン含有樹
脂の安定化剤(特開昭51−12847)として用いら
れることは知られているが、化粧用粉体としての
利用に関してはなんら開示されておらず、本発明
者らによつて始めてて見いだされたものである。
Conventionally, N-acyl lysine or its metal salt has been used as an amphoteric surfactant in detergents (Japanese Patent Application Laid-Open No. 1983-
97605) or as a stabilizer for halogen-containing resins such as polyvinyl chloride (Japanese Unexamined Patent Publication No. 51-12847), but nothing has been disclosed regarding its use as a cosmetic powder. This was discovered for the first time by the present inventors.

本発明のN−アシルリジンは、その構造より明
らかなごとく、天然由来のリジンと脂肪酸とから
成り、皮膚蛋白質と同様アミド基を有する為、皮
膚に対する刺激性が少なく、しかも優れた吸着
力、被覆力を示す。また、分子中に疎水基である
炭化水素鎖と、親水基であるアミノ基、カルボキ
シル基を有し、導入するアシル基の数及びその鎖
長を変えることによつて容易に親水基と疎水基の
バランスを変えることが出来る。この為各種化粧
料に配合した場合、油性基材すなわち油との相溶
性のある基材、或は水性基材すなわち水との相溶
性のある基材への分散性又は人体の皮膚表面にお
かれた場合、汗や分秘物等の吸収性を調整するこ
とができ、目的の化粧品の物性に合わせたN−ア
シルリジンの選択が可能となるなど、画期的な化
粧用粉体であるといえる。かかる粉体は、単独で
用いられるほか、他の化粧用粉体と併用した場合
でも、上述した特質をいかんなく発揮する。油性
基材としてはミツロウ、木ロウ、鯨ロウ、カルナ
バロウ、キヤンデリラロウ、カカオ脂、セチルア
ルコール、ステアリルアルコール、オレイン酸、
ステアリン酸、ラノリン、オリーブオイル、ツバ
キ油、綿実油、ヒマシ油、オレイルアルコール、
スクアラン、等の動値物油や、固形パラフイン、
セレシン、マイクロクリスタリンワツクス、ワセ
リン、流動パラフイン、シリコーンオイルとうの
鉱物系油脂、及びイソプロピルミリステアート、
合成ポリエーテル等の合成系油脂が、一方水性基
材としてはグリセリン、プロピレングリコール、
ソルビツト、ポリエチレングリコール、クインス
シードゴム、トランガムゴム、アルギン酸塩、ペ
クチン、カルボキシメチルセルロース、ヒアルロ
ン酸、キトサン、ポリビニルアルコール、エタノ
ール、イソプロパノール、クエン酸、尿素、カオ
チン化セルロース脂肪酸ボリペプチド縮合物、乳
酸、ピロリドン、カルボン酸塩、各種アミノ酸等
が挙げられる。
As is clear from its structure, the N-acyl lysine of the present invention is composed of naturally derived lysine and fatty acids, and has an amide group similar to skin proteins, so it is less irritating to the skin and has excellent adsorption and covering power. shows. In addition, it has a hydrocarbon chain, which is a hydrophobic group, and an amino group and a carboxyl group, which are hydrophilic groups, in the molecule, and by changing the number of acyl groups to be introduced and the chain length, it is possible to easily combine hydrophilic and hydrophobic groups. can change the balance of For this reason, when incorporated into various cosmetics, it is difficult to disperse into oil-based base materials, that is, base materials that are compatible with oil, or water-based base materials, that is, base materials that are compatible with water, or on the skin surface of the human body. It is a revolutionary cosmetic powder that can adjust the absorption of sweat and secretions, and allows the selection of N-acyl lysine that matches the physical properties of the desired cosmetic product. I can say that. Such a powder fully exhibits the above-mentioned characteristics when used alone or in combination with other cosmetic powders. Oil-based base materials include beeswax, wood wax, spermaceti wax, carnauba wax, candelilla wax, cacao butter, cetyl alcohol, stearyl alcohol, oleic acid,
Stearic acid, lanolin, olive oil, camellia oil, cottonseed oil, castor oil, oleyl alcohol,
Animal oils such as squalane, solid paraffin,
Ceresin, microcrystalline wax, petrolatum, liquid paraffin, mineral oils and fats such as silicone oil, and isopropyl myristate,
Synthetic oils and fats such as synthetic polyether are used, while aqueous base materials include glycerin, propylene glycol,
Sorbit, polyethylene glycol, quince seed gum, tranguum gum, alginate, pectin, carboxymethylcellulose, hyaluronic acid, chitosan, polyvinyl alcohol, ethanol, isopropanol, citric acid, urea, cationized cellulose fatty acid polypeptide condensate, lactic acid, pyrrolidone, carvone Examples include acid salts and various amino acids.

本発明の対象となる化粧料としては、各種クリ
ーム、ローシヨン、粉白粉、練り白粉、固形白
粉、ボデイパウダー、ベビイパウダー、制汗剤、
フアウンデイシヨン、練り歯みがき等のほか、化
粧料中に粉体が含まれているものであればよい。
Cosmetics covered by the present invention include various creams, lotions, white powders, white powders, solid white powders, body powders, baby powders, antiperspirants,
In addition to foundations, toothpaste, etc., cosmetics containing powder may be used.

以下、実施例により更に詳しく説明する。 A more detailed explanation will be given below using examples.

実施例 1 粉白粉 N〓−ヘキサノイルリジン 35.0重量% N〓−パルミトイルリジン 30.0 N〓−N〓−ジラウロイルリジン 35.0 香 料 適量 ボールミルを用い、上記配合比に基づいて各種
N−アシルリジンを充分混合粉砕し、粉白粉を調
製した。かかる粉白粉は安全性に優れ、また使用
感及び皮膚に対する吸着力、被覆力等も良好であ
つた。
Example 1 Flour powder N-hexanoyl lysine 35.0% by weight N-palmitoyl lysine 30.0 N-N-dilauroyl lysine 35.0 Flavor Appropriate amount Using a ball mill, various N-acyl lysines were thoroughly mixed based on the above blending ratio. It was ground to prepare white powder. This white powder was excellent in safety, and also had good feel on use, good adhesion to the skin, good covering power, etc.

実施例 2 粉白粉 N〓−ラウロイルリジン 40.0重量% タルク 43.0 カオリン 10.0 沈降性炭酸カルシウム 2.0 亜鉛華 2.0 ステアリン酸亜鉛 2.0 炭酸マグネシウム 1.0 色素・顔料 適量 香 料 適量 ボールミルを用い、上記配合比に基づいて各種
粉末原料を充分混合粉砕し、粉白粉を調製した。
かかる粉白粉は、皮膚に対する吸着力、分泌物吸
着性に優れ、また感触も良好であつた。
Example 2 Powder powder N - lauroyl lysine 40.0% by weight Talc 43.0 Kaolin 10.0 Precipitated calcium carbonate 2.0 Zinc white 2.0 Zinc stearate 2.0 Magnesium carbonate 1.0 Color/Pigment Appropriate amount Flavor Appropriate amount Using a ball mill, various types were prepared based on the above compounding ratio. The powder raw materials were thoroughly mixed and ground to prepare white powder.
This white powder had excellent adhesion to the skin and adsorption of secretions, and also had a good feel.

実施例 3 練り白粉 N〓−ココイルリジン 40.0重量% ナイロン12パウダー 20.0 グリセリン 10.0 ピロリドンカルボン酸ソーダ 3.0 精製水 27.0 色素・香料 適量 奈良式粉砕機を用いて200メツシユ以上に粉砕
したN〓−ココイルリジン、グリセリン、ピロリ
ドンカルボン酸ソーダ、精製水を加え、乳化機を
用いて混練し、練り白粉を得た。
Example 3 Kneaded white powder N-cocoyl lysine 40.0% by weight Nylon 12 powder 20.0 Glycerin 10.0 Sodium pyrrolidone carboxylate 3.0 Purified water 27.0 Coloring matter/fragrance Appropriate amount N-cocoyl lysine ground to 200 mesh or more using a Nara type grinder, Glycerin, sodium pyrrolidone carboxylate, and purified water were added and kneaded using an emulsifying machine to obtain white powder.

かかる練り白粉は、皮膚に対する伸び、被覆力
が良好で、化粧崩れが起り難いという特徴を有す
る。
Such a white powder has good spreadability and covering power on the skin, and has the characteristics that it does not easily cause makeup to come off.

実施例 4 固形白粉 N〓−ステアロイルリジン 20.0重量% N〓−ステアロイルリジン 20.0 N〓−N〓−ジステアロイルリジン 10.0 タルク 10.0 亜鉛華 10.0 カオリン 10.0 ステアリン酸亜鉛 5.0 炭酸マグネシウム 5.0 トラガントガム水溶液 7.0 ピロリドンカルボン酸ソーダ 3.0 色素・顔料 適量 香 料 適量 上記の各種の粉体原料を、ボールミルにて充分
混合粉砕し、結合剤としてトラガントガム水溶液
及びピロリドンカルボン酸ソーダを加えた後、プ
レス成型して固形白粉とした。かかる固形白粉
は、成型加工が容易でヒビ割れが起り難く、使用
時の感触も良好であつた。
Example 4 Solid white powder N〓-stearoyl lysine 20.0% by weight N〓-stearoyl lysine 20.0 N〓-N〓-distearoyl lysine 10.0 Talc 10.0 Zinc white 10.0 Kaolin 10.0 Zinc stearate 5.0 Magnesium carbonate 5.0 Gum tragacanth aqueous solution 7.0 Sodium pyrrolidone carboxylate 3.0 Coloring matter/Pigment Appropriate amount Fragrance Appropriate amount The above various powder raw materials were sufficiently mixed and ground in a ball mill, and after adding an aqueous solution of gum tragacanth and sodium pyrrolidone carboxylate as a binder, press molding was performed to obtain a solid white powder. This solid white powder was easy to mold, was less prone to cracking, and had a good feel when used.

実施例 5 アイシヤドウ N〓−ステアロイルリジン 8.0重量% タルク 1.0 顔 料 12.0 パール剤 18.0 白色ワセリン 12.0 ラノリン誘導体 5.0 マイクロクリスタリンワツクス 15.0 スクワラン 2.0 流動パラフイン 27.0 奈良式粉砕機により、200メツシユ以上に粉砕
したN〓−ステアロイルリジンに、上記各成分を
加え、乳化機を用いて充分混練し、アイシヤドウ
を調製した。かかるアイシヤドウは、皮膚への吸
着性が良く化粧崩れが起り難いという特徴を有す
る。
実施例 5 アイシヤドウN〓−ステアロイルリジン 8.0重量% タルク 1.0 顔 料 12.0 パール剤 18.0 白色ワセリン 12.0 ラノリン誘導体 5.0 マイクロクリスタリンワツクス 15.0 スクワラン 2.0 流動パラフイン 27.0 奈良式粉砕機により、200メツシユ以上に粉砕したN〓 - The above ingredients were added to stearoyl lysine and thoroughly kneaded using an emulsifier to prepare eyelid dough. Such eye shadow powder has a characteristic that it has good adsorption to the skin and does not easily cause makeup to come off.

実施例 6 フアンデーシヨンローシヨン 油 相 ステアリン酸 2.5% プロピレングリコール・モノステアレート
6.0% 流動パラフイン 5.0 水 相 精製すい 53.1 トリエタノールアミン 1.3 パラヒドロキシ安息香酸メチル 0.1 固 相 ラウリル硫酸ナトリウム 1.1 ベントナイト 4.7 カオリン 5.2 着色粉末原料 11.0 N〓−ラウロイルリジン 10.0 香 料 適量 固相成分を奈良式粉砕機により、200メツシユ
以上にそれぞれ粉砕する。これに精製水を、さら
に水相成分を加え、さらに油相成分を乳化機を用
いて加え混練する。かかる製品は皮膚の表面にな
めらかにのび、引続く化粧仕上げをしやすくする
特徴を有する。
Example 6 Foundation lotion oil Phase stearic acid 2.5% Propylene glycol monostearate
6.0% Liquid paraffin 5.0 Water Phase purified water 53.1 Triethanolamine 1.3 Methyl parahydroxybenzoate 0.1 Solid phase Sodium lauryl sulfate 1.1 Bentonite 4.7 Kaolin 5.2 Colored powder raw material 11.0 N-Lauroyl lysine 10.0 Flavor Appropriate amount Solid phase components are crushed by Nara method Grind each piece into 200 mesh pieces or more using a machine. Purified water is added to this, a water phase component is added, and an oil phase component is further added using an emulsifying machine and kneaded. Such products have the characteristic of spreading smoothly onto the skin surface and facilitating subsequent makeup application.

実施例 7 クレンジングクリーム 油 相 流動パラフイン 20.0% ミツロウ 10.0 植物油 25.0 ソルビタンモノステアレート(注1) 5.0 ラノリン 3.0 N〓−ラウロイルリジン 10.0 水 相 ポリオキシエチレンソルビタンモノステアレー
ト(注2) 2.0 ホウ砂 0.7 精製水 24.3 香 料 適量 保存剤 適量 (注1)Arlacel60 (注2)Tween60 乳化機に油相成分を入れ、これに水を次に水相
成分を除々に加え充分混練した。かかるクレンジ
ングクリームは皮膚の上でのびのあるクリームで
あつた。
Example 7 Cleansing cream oil Phase fluid paraffin 20.0% Beeswax 10.0 Vegetable oil 25.0 Sorbitan monostearate (Note 1) 5.0 Lanolin 3.0 N-lauroyl lysine 10.0 Water Phase polyoxyethylene sorbitan monostearate (Note 2) 2.0 Borax 0.7 Purification Water 24.3 Flavor Appropriate amount Preservative Appropriate amount (Note 1) Arlacel 60 (Note 2) Tween 60 Put the oil phase components into an emulsifier, add water, then gradually add the water phase components and mix thoroughly. This cleansing cream was a cream that spread easily on the skin.

実施例 8 オールパーパスクリーム 油 相 アミテルLGOD 9.0% スクワラン 9.0 鯨ロウ 2.0 プロピレングリコールモノステアレート 4.0 POE(20)グリセリルモノステアレート 3.0 グリセリルモノステアレート(自己乳化型)
10.0 ソルビタンモノステアレート 1.5 N〓−ラウロイルリジン 2.0 水 相 PCAソーダ(50%) 2.0 ソルビトール(70%) 4.0 防腐剤 0.3 精製水 53.2 油相成分を80℃で撹拌しつつ水相成分を除々に
加える後冷却する、皮膚になじみ、べたつかず、
よくのびる特徴があつた。
Example 8 All-purpose cream oil Phase Amitel LGOD 9.0% Squalane 9.0 Sperm wax 2.0 Propylene glycol monostearate 4.0 POE (20) Glyceryl monostearate 3.0 Glyceryl monostearate (self-emulsifying type)
10.0 Sorbitan Monostearate 1.5 N〓-Lauroyl Lysine 2.0 Water Phase PCA Soda (50%) 2.0 Sorbitol (70%) 4.0 Preservative 0.3 Purified Water 53.2 While stirring the oil phase components at 80℃, gradually add the water phase components. After cooling, it blends into the skin and is non-sticky.
It has a characteristic that it spreads well.

実施例 9 コールドクリーム 油 相 サラミツロウ 18.0% アーモンド油 61.0 N〓−ラウロイルリジン 4.0 ローズ油 1.0 水 相 ホウ砂 1.0 ローズ水 15.0 乳化機中に油相成分を入れ、これに除々にロー
ズ水を加えよく乳化する。次にホウ砂を加えよく
混練する。
Example 9 Cold cream oil Phase beeswax 18.0% Almond oil 61.0 N - lauroyl lysine 4.0 Rose oil 1.0 Water Phase borax 1.0 Rose water 15.0 Put the oil phase ingredients into an emulsifier, and gradually add rose water to it. Emulsify. Next, add borax and mix well.

肌によくなじむコールドクリームが得られた。 A cold cream that blends well with the skin was obtained.

実施例 10 ミルクローシヨン 油 相 流動パラフイン 31.6% 固形パラフイン 4.5 セタノール 4.0 ソルビタモノステアレート 1.8 POE(20)ソルビタモノオレート 2.8 N〓−ラウロイルリジン 1.0 水 相 PCA−トリエタノールアミン(50%) 4.0 精製水 50.1 防腐剤 0.2 乳化機に水相成分を入れ80℃に加温した後油相
成分を除々に加え混練した。かかる製品は肌にべ
とつかないさわやかさを与ええる特徴を有した。
Example 10 Milk lotion oil Phase fluid paraffin 31.6% Solid paraffin 4.5 Setanol 4.0 Sorbita monostearate 1.8 POE (20) Sorbita monooleate 2.8 N-Lauroyl Lysine 1.0 Water Phase PCA-triethanolamine (50%) 4.0 Purified water 50.1 Preservative 0.2 The water phase components were placed in an emulsifier and heated to 80°C, and then the oil phase components were gradually added and kneaded. Such a product had the characteristic of being able to provide refreshing, non-sticky skin to the skin.

Claims (1)

【特許請求の範囲】 1 下記一般式(1)乃至(3)で表わされるN−アシル
リジンの少なくとも一種を粉末形態で配合してな
る化粧料。 (但し、一般式(1)および(2)に於いてRCOは、炭
素数8乃至22の脂肪族アシル基を示す。また、一
般式(3)に於いてR′COとR″COはそれぞれ炭素数
1乃至22であつて両者の合計が9乃至44となる脂
肪族アシル基を示す。)
[Scope of Claims] 1. A cosmetic comprising at least one N-acyl lysine represented by the following general formulas (1) to (3) in powder form. (However, in general formulas (1) and (2), RCO represents an aliphatic acyl group having 8 to 22 carbon atoms. In addition, in general formula (3), R′CO and R″CO respectively Indicates an aliphatic acyl group having 1 to 22 carbon atoms and a total of 9 to 44.)
JP17570883A 1983-09-22 1983-09-22 Cosmetic Granted JPS6067406A (en)

Priority Applications (4)

Application Number Priority Date Filing Date Title
JP17570883A JPS6067406A (en) 1983-09-22 1983-09-22 Cosmetic
EP19840306449 EP0139481B1 (en) 1983-09-22 1984-09-21 Surface modification using n-acyl lysines
US06/653,024 US4640943A (en) 1983-09-22 1984-09-21 Surface modifier for inorganic substances
DE8484306449T DE3485717D1 (en) 1983-09-22 1984-09-21 SURFACE CHANGE WITH THE AID OF N-ACYL LYSINES.

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP17570883A JPS6067406A (en) 1983-09-22 1983-09-22 Cosmetic

Publications (2)

Publication Number Publication Date
JPS6067406A JPS6067406A (en) 1985-04-17
JPH0216725B2 true JPH0216725B2 (en) 1990-04-18

Family

ID=16000851

Family Applications (1)

Application Number Title Priority Date Filing Date
JP17570883A Granted JPS6067406A (en) 1983-09-22 1983-09-22 Cosmetic

Country Status (1)

Country Link
JP (1) JPS6067406A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2006306859A (en) * 2005-03-30 2006-11-09 Ajinomoto Co Inc Cosmetic powder
JP2012153728A (en) * 2005-03-30 2012-08-16 Ajinomoto Co Inc Cosmetic powder

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS61137808A (en) * 1984-12-07 1986-06-25 Ajinomoto Co Inc Cosmetic composition for skin and hair
JPH0644758A (en) * 1992-02-03 1994-02-18 Nippon Columbia Co Ltd Device for reproducing musical sound
DE112014001299T8 (en) * 2013-03-14 2016-02-25 Ajinomoto Co., Inc. Cosmetic composition
JP6686905B2 (en) 2014-12-25 2020-04-22 味の素株式会社 Hair cosmetic composition containing an acyl basic amino acid derivative
JP2017197559A (en) * 2017-06-09 2017-11-02 味の素株式会社 Composite powders and makeup cosmetics

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5128610A (en) * 1974-09-04 1976-03-11 Hitachi Ltd Museiryushimoota no sokudoseigyokairo

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5128610A (en) * 1974-09-04 1976-03-11 Hitachi Ltd Museiryushimoota no sokudoseigyokairo

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2006306859A (en) * 2005-03-30 2006-11-09 Ajinomoto Co Inc Cosmetic powder
JP2012153728A (en) * 2005-03-30 2012-08-16 Ajinomoto Co Inc Cosmetic powder

Also Published As

Publication number Publication date
JPS6067406A (en) 1985-04-17

Similar Documents

Publication Publication Date Title
JP5155658B2 (en) Surface-treated powder and cosmetics containing the same
US5665687A (en) Cleaning composition containing lipid grains
US11896684B2 (en) Cosmetic composition having increased skin contact and makeup persistence and method of manufacturing same
KR19990063353A (en) Cosmetic composition
JP5639067B2 (en) Cosmetic pigment, method for producing the same, and cosmetic containing the cosmetic pigment
JP2003048846A (en) Collagenase inhibitor and antiaging cosmetic
WO2017188279A1 (en) Composition for cosmetics and cosmetic comprising same
JP2003055190A (en) Collagenase inhibitor and anti-ageing cosmetic
JP2002515412A (en) Composition for topical application
JPH0216725B2 (en)
JP2002205916A (en) Cosmetic
JP2003034631A (en) Fibroblast proliferation-promoting agent and aging- preventing cosmetics
JP3529695B2 (en) Composite powder and cosmetics
JP2012201683A (en) Cosmetic
JP4183422B2 (en) Topical preparation
WO2022145471A1 (en) Powder composition for cosmetics or skin topical agent, and production method therefor
JP3784723B2 (en) Topical preparation
JP3442698B2 (en) Manufacturing method of cosmetics
JP4111766B2 (en) Skin preparation
EP4029572A1 (en) Powder surface treatment method, surface treating agent composition used therefor, and surface-treated powder
KR100434854B1 (en) A Silica Composition Containing an Aloe and a Cosmetic Composition Containing a Silica Composition and Method of Manufacturing a Cosmetic Composition Utilizing Aloe
JP2003055131A (en) Cosmetic composition
KR100961400B1 (en) Cosmetic composition
JP2780805B2 (en) New skin external preparation composition
JPS6115811A (en) Cosmetic