JPS59134707A - Cosmetic - Google Patents

Cosmetic

Info

Publication number
JPS59134707A
JPS59134707A JP768983A JP768983A JPS59134707A JP S59134707 A JPS59134707 A JP S59134707A JP 768983 A JP768983 A JP 768983A JP 768983 A JP768983 A JP 768983A JP S59134707 A JPS59134707 A JP S59134707A
Authority
JP
Japan
Prior art keywords
urea
cosmetic
amino acids
aminoacids
present
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
JP768983A
Other languages
Japanese (ja)
Other versions
JPH0456002B2 (en
Inventor
Takeshi Yanagida
威 柳田
Tsuneo Takayabu
恒雄 高藪
Masako Iwai
岩井 真子
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 JP768983A priority Critical patent/JPS59134707A/en
Publication of JPS59134707A publication Critical patent/JPS59134707A/en
Publication of JPH0456002B2 publication Critical patent/JPH0456002B2/ja
Granted legal-status Critical Current

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q19/00Preparations for care of the skin
    • 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
    • A61K8/42Amides
    • 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
    • A61Q5/00Preparations for care of the hair
    • A61Q5/02Preparations for cleaning the hair

Abstract

PURPOSE:A cosmetic that is prepared by adding a specific aminoacid to urea, thus increasing the stability of urea with time and allowing the urea to exhibit its intrinsic properties of humectation, cell activation and wound curing satisfactorily. CONSTITUTION:The objective cosmetic is composed of urea and more than 1/ 10pts.wt., based on the urea, of at least one selected from neutral aminoacids, acidic aminoacids and alkali metal salts of acidic aminoacids. EFFECT:It is free from ammoniac smell and scarcely causes increase in pH. USE:A base cosmetic for lotion, cream, emulsion, pack, make-up cosmetic such as emulsified lip sticks, foundations, or hair cosmetics such as shampoo or rinse.

Description

【発明の詳細な説明】 本発明は尿素と共にアミノ酸を配合することにより尿素
の経I:1安定性を向上させた化■1料に関するもので
ある。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a compound (1) in which the stability of urea is improved by blending an amino acid with urea.

尿素は化粧相中に配合した場合、湿潤効果、細胞賦活効
果、創傷泊ゆ効果等が期待される。しかしながら水の共
存化で徐々に分解し、アンモニア及び炭酸ガスを発生す
るため種々の効果が期待されつつも化粧料に配合される
機会が少なかった。
When urea is incorporated into a cosmetic phase, it is expected to have a moisturizing effect, a cell activation effect, a wound soothing effect, etc. However, in the presence of water, it gradually decomposes and generates ammonia and carbon dioxide gas, so although it is expected to have various effects, it has rarely been incorporated into cosmetics.

本発明者らはかかる事情にかんがみ鋭意研究の結果、尿
素と共に特定のアミノ酸を配合することにより尿素の経
日安定性を向上させられること−を見い出し、本発明を
なすに至った。
In view of the above circumstances, the present inventors have conducted extensive research and have discovered that the stability of urea over time can be improved by blending a specific amino acid with urea, leading to the present invention.

すなわち本発明は、(1)尿素と、(ii)中性アミノ
酸、酸性アミノ酸および酸性アミノ酸のアルカリ塩から
なる群より選ばれた1種又は2種以上を配合することを
特徴とする化粧料を提供するものである。
That is, the present invention provides a cosmetic product that contains (1) urea and (ii) one or more selected from the group consisting of neutral amino acids, acidic amino acids, and alkali salts of acidic amino acids. This is what we provide.

以下本発明の構成について1倉述する。The configuration of the present invention will be briefly described below.

本発明で用い°られる尿素としては通常市販されている
もの、でかまわない。
The urea used in the present invention may be any commercially available urea.

尿素の配合1dは01〜5重鼠%の範囲で、それ以下の
水1■では前述の尿素の皮フに対する効果が少なく、ま
たそれ以上の水阜は蘂・If法−Jl、化1フ1品の範
囲を逸脱するものであり、規制を受ける。
The urea formulation 1d is in the range of 01 to 5%.If the water is less than 1%, the effect of urea on the skin will be small, and if the water is more than that, the urea method-Jl, chemical 1% will be less effective. It is outside the scope of one product and is subject to regulations.

本発明で用いられるアミノ酸は中性アミノ酸わよび酸性
アミノ酸であり、例示すれば、グリシン、アラニン、セ
リン、バリン、トレオニン、アスパラギン酸、グルタミ
ン酸等である。
The amino acids used in the present invention are neutral amino acids and acidic amino acids, such as glycine, alanine, serine, valine, threonine, aspartic acid, and glutamic acid.

酸性アミノ酸はアルカリ塩の形で用いられても構わない
。塩の対イオンは任意のもので〜良く、例えばナトリウ
ム塩・カリウム塩・ リチウム塩等の無機アルカリ1ア
ルギニン塩1リジン塩1ヒスチジン塩、オルニチン塩等
の塩基性アミノ酸、トリエタノールアミン等の塩基性ア
ミン等の塩を挙げることができる。これらの塩の中では
ナトリウム塩、ノJリウム塩がとくに好ましい。
Acidic amino acids may be used in the form of alkaline salts. The counter ion of the salt may be any one, such as an inorganic alkali such as sodium salt, potassium salt, or lithium salt, 1 arginine salt, 1 lysine salt, 1 basic amino acid such as histidine salt, ornithine salt, or basic amino acid such as triethanolamine. Salts of amines and the like can be mentioned. Among these salts, sodium salts and sodium salts are particularly preferred.

本発明においては、上記の中性アミノ酸、酸性アミノ酸
および酸性アミノ酸のアルカリ塩のうちから任意の1種
又は2種以上が選ばれて用いられるO 配合されるアミノ酸の量は、尿、;〈に対し1/10屯
:11以」−が安定性向上の為に望ましい。世し過剰の
アミノ酸の添加はアミノ酸自身が変質し・変色・変臭等
を生・しるために注意が必要である。
In the present invention, one or more of the above-mentioned neutral amino acids, acidic amino acids, and alkali salts of acidic amino acids are selected and used. On the other hand, 1/10 ton: 11" or more is desirable for improving stability. Care must be taken when adding excessive amounts of amino acids, as the amino acids themselves may deteriorate, resulting in discoloration, odor, etc.

尿素及びγミノ継を配合できる化粧料基剤は通常考えら
れる化粧料基剤、例えば、可溶化系、乳化系、粉末分散
系、水−油系2層状化粧料、水−油一粉末系3層状化翌
1.料等どのような基剤でもよく、用途も化粧水、乳液
、クリーム・パック等の基礎化粧料、乳化1」紅、フ7
ウンディション等のメイクアップ化粧料、シャンプー、
リンス、ヘアトニック等の頭髪化粧料)多岐に渡るが、
本発明の効果は、尿素が水溶液の形で含まれているj9
 t/)において発揮される。尿士水溶液の濃度は任意
である。又、上述の如く尿素水溶液が油相と乳化された
形等になっていても全く差支えなく本発明の効果は発揮
される。しかしながら、塙剤1乍身が塩基性を示すもの
については7′ミノ酸による安定性維持効果以上に塩基
性物質による分解促進のh′が大きい一場合があり、好
ましくない。
Cosmetic bases in which urea and γ-minotsugi can be blended include commonly thought cosmetic bases, such as solubilized systems, emulsified systems, powder dispersion systems, water-oil two-layer cosmetics, and water-oil one-powder systems. After layering 1. Any base material may be used, and it can be used for basic cosmetics such as lotions, emulsions, cream packs, emulsifiers, etc.
Make-up cosmetics, shampoo, etc.
hair cosmetics such as conditioners and hair tonics)
The effect of the present invention is that urea is contained in the form of an aqueous solution.
t/). The concentration of the urinary tract aqueous solution is arbitrary. Further, as described above, even if the urea aqueous solution is in the form of an emulsion with the oil phase, there is no problem and the effects of the present invention can be exhibited. However, if the bulking agent itself is basic, the acceleration of decomposition by the basic substance h' may be greater than the stability maintaining effect by the 7' amino acid, which is not preferable.

本発明の化粧料には必要に応して・本発明の効果を損な
わない範囲で保湿剤、増粘剤、防腐剤、乳化剤、醸化防
止剤、金属イオン封鎖剤、紫外線吸収剤、粉末、助動成
分・色剤、香料秀を配合することができる。
The cosmetics of the present invention may contain humectants, thickeners, preservatives, emulsifiers, anti-aging agents, sequestering agents, ultraviolet absorbers, powders, etc., as necessary, within the range that does not impair the effects of the present invention. Auxiliary ingredients, colorants, and fragrances can be added.

本発明に従って化粧料中に尿素と’4¥定のアミノ酸を
同時に配合した場合の尿素の紅1−1安定性は、アミノ
酸を併用しない場合に比較して著しく向上する。すなわ
ち、1)尿素の分解によるγンモニが急激に−L昇する
が、併用した場合にはpH−h昇がほとんどおこらない
等の効果が認められる◇ナオ、アミノ酸ではあってもヒ
スチジン、アルギニン窩の塩基性アミノ酸では、本発明
の効果は得ることができない。
According to the present invention, when urea and a 40% amino acid are simultaneously blended into a cosmetic, the urea's red 1-1 stability is significantly improved compared to when the amino acid is not used in combination. In other words, 1) γ-monitoring due to decomposition of urea rapidly increases -L, but when used in combination, there is an effect such that pH-H hardly increases. The effects of the present invention cannot be obtained with basic amino acids such as

次に本発明を実施倒産び比較例によりさらに詳細に説明
するが、本発明はこれにより限定されるものではない。
Next, the present invention will be explained in more detail with reference to practical failures and comparative examples, but the present invention is not limited thereto.

(以下余白) 実施例1〜3、比較例1〜3 ■ ■ 〔基材−化粧水〕 エタノール             13.0wt%
1.3−ブチレングリコール       1o、。
(Margin below) Examples 1 to 3, Comparative Examples 1 to 3 ■ ■ [Base material - Lotion] Ethanol 13.0wt%
1.3-Butylene glycol 1o.

P、O,E(50)オレイルエーテル        
08防腐剤               適:1に香
  料                      
   適;1″L」−記名成分と尿素及び添加剤を加え
、さらに全量を100とする量の精製水を加える。
P, O, E (50) oleyl ether
08 Preservatives Suitability: 1 Fragrance
Suitable: 1"L" - Add the registered ingredients, urea and additives, and add purified water in an amount to make the total volume 100.

匂い変化・・・50°C1力月保存品の匂い。Cノ印は
アンモニア臭なし。X印はアンモニア臭あり。
Odor change: Odor of product stored at 50°C for 1 month. C mark indicates no ammonia odor. The X mark has an ammonia odor.

尿素の定)iY値・・・・50″C1力月保存品の尿素
の定jI’、c 値。高速液体クロマトグラフィー法に
よる。
Determination of urea) iY value...50''C1 Determination of urea jI', c value of stored product. Based on high performance liquid chromatography method.

ミノ酸を添加した例、すなわち実施例1.2.3と比較
すると、p11変化、アンモニア某、定;1;:値等−
の評価項1−1が格段に劣る。pH変化、匂い変化共G
こ少ない方が望ましく、定量値は高い方が望ましいわけ
であるが、実施例においてはこのいずれをも〔実施例4
〕 ナイトクリーム    (重量%)A、 セタノー
ル            40ワセリン      
        70スクワラン          
 21.0グリセリンモ/脂肪酸エステル     z
2Tween60                j
?、8イソプロピルミリステート60 エチルパラベン          03香料    
          02B、グリセリン      
    100プロピレングリコール       5
0尿素               30グリシン 
           2+0精製水        
     365Aに属する油相部の原料およびBに属
する水相部の原料をそれぞれ70°Cに加熱し、完全溶
解したのち、油相部を水相部中に混合し、乳化機にて乳
化する。乳化物を熱交換機にて終i7..’、 30 
’Cまで冷却したのち充てんを行なう。
When compared with the example in which amino acid was added, that is, Example 1.2.3, p11 change, ammonia, constant; 1;: value, etc.
Evaluation item 1-1 is significantly inferior. Both pH change and odor change
It is preferable to have a lower quantitative value, and a higher quantitative value is preferable.
] Night cream (weight%) A, Setanol 40 Vaseline
70 squalane
21.0 Glycerin mo/fatty acid ester z
2Tween60 j
? , 8 Isopropyl myristate 60 Ethylparaben 03 Fragrance
02B, glycerin
100 propylene glycol 5
0 urea 30 glycine
2+0 purified water
The raw material for the oil phase belonging to 365A and the raw material for the aqueous phase belonging to B are heated to 70°C and completely dissolved, and then the oil phase is mixed into the water phase and emulsified using an emulsifier. Finish the emulsion using a heat exchanger i7. .. ', 30
After cooling to 'C, filling is performed.

実施例4に記載された処方からアミノ酸のみを除去した
処方を実施例4と同時に調製し、40°Cにて2力月保
存したのち尿素の定はを行なったところ実施例4では9
7〜99%残存していたのに対し、アミノ酸を除去した
ものは86〜88%に減少していた。
A formulation in which only amino acids were removed from the formulation described in Example 4 was prepared at the same time as Example 4, and after being stored at 40°C for 2 months, urea was determined.
While 7 to 99% remained, those from which amino acids were removed decreased to 86 to 88%.

(以下余白) 実施例5 ファウンデーンヨン   (重量%)A、 
セタノール            35脱臭う/リン
           40ホホバ油        
     50ワセリン             Z
、0スクワラン            6゜グリセリ
ン脂肪酸エステル     2−5P、 O,E、 (
60)硬化ヒマン油     15P、 O,E、 (
25)セチルニーデル    10プロピルパラベン 
        03香f11.          
    0.2B、 グリセリン          
 30プロピレングリコール       800.3
2wt%、Fe、O,0,08wt95.Fe0(OH
)0.4wt%)尿素              2
−Oアラニン             20グルタミ
ン酸モノナトリウム    lO精製水       
      、60製造方法は実施例5に準する。
(Left below) Example 5 Foundryon (wt%) A,
Setanol 35 Deodorizing/phosphorus 40 Jojoba oil
50 Vaseline Z
, 0 squalane 6゜glycerin fatty acid ester 2-5P, O, E, (
60) Hydrogenated human oil 15P, O, E, (
25) Cetylneedle 10propylparaben
03 incense f11.
0.2B, glycerin
30 Propylene Glycol 800.3
2wt%, Fe, O, 0.08wt95. Fe0(OH
)0.4wt%) Urea 2
-O alanine 20 monosodium glutamate lO purified water
, 60 manufacturing method is based on Example 5.

実施例5に記載された処方よりアミノ酸のみを除去した
処方を処方例2と同時に調製し、0°Cにて2力月保存
したのち尿素の定量を行なったところ実施例5では96
〜98%残存していたのに対し、アミノ酸を除去したも
のは89〜90%に減少していた。
A formulation in which only amino acids were removed from the formulation described in Example 5 was prepared at the same time as Formulation Example 2, and after storage at 0°C for 2 months, urea was quantified.
~98% remained, whereas that from which amino acids were removed was reduced to 89-90%.

特許出願人  株式会社賢生堂 手続補正書(自発) ロア(■ll 58年12刀90 特許庁長官 名 杉 和 人 殿 1、 事件の表示 昭和58年特許願第7689号 2、 発明の名称 化粧料 3、補正をする考 4、補正の対象 明細書の発明の詳細な説明の欄 (1>明細書第6頁の表中、比較例2の行の薬品名の列
に「乳」とあるを、「乳酸」と袖正します。
Patent Applicant Kenseido Co., Ltd. Procedural Amendment (Voluntary) Roa (■ll 1958 12 Swords 90 Commissioner of the Patent Office Name Kazuto Sugi 1, Indication of Case 1982 Patent Application No. 7689 2, Name of Invention Cosmetics 3. Consideration for amendment 4. Detailed explanation of the invention in the specification subject to amendment , "lactic acid," he says.

以     上that's all

Claims (1)

【特許請求の範囲】[Claims] (1)尿素と、(ii)中性アミノ酸、酸性アミノ酸お
よび酸性アミノ酸のアルカリ塩からなる群より選ばれた
1種または2種以上を配合することを特徴とする化和1
料。
Chemical formula 1 characterized in that it contains (1) urea and (ii) one or more selected from the group consisting of neutral amino acids, acidic amino acids, and alkali salts of acidic amino acids.
fee.
JP768983A 1983-01-20 1983-01-20 Cosmetic Granted JPS59134707A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP768983A JPS59134707A (en) 1983-01-20 1983-01-20 Cosmetic

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP768983A JPS59134707A (en) 1983-01-20 1983-01-20 Cosmetic

Publications (2)

Publication Number Publication Date
JPS59134707A true JPS59134707A (en) 1984-08-02
JPH0456002B2 JPH0456002B2 (en) 1992-09-07

Family

ID=11672748

Family Applications (1)

Application Number Title Priority Date Filing Date
JP768983A Granted JPS59134707A (en) 1983-01-20 1983-01-20 Cosmetic

Country Status (1)

Country Link
JP (1) JPS59134707A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2002167328A (en) * 2000-11-29 2002-06-11 Toyo Aerosol Ind Co Ltd Composition and aerosol composition for external skin preparation
CN105439907A (en) * 2015-12-02 2016-03-30 锦西天然气化工有限责任公司 Production technology of stable urea
US10073104B2 (en) 2013-03-14 2018-09-11 Siemens Healthcare Diagnostics Inc. Control of pH in aqueous urea-containing solutions utilizing amino acid-containing compositions
WO2020251017A1 (en) * 2019-06-14 2020-12-17 ゼリア新薬工業株式会社 Composition for external application

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
CHEMICAL ABSTRACTS *

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2002167328A (en) * 2000-11-29 2002-06-11 Toyo Aerosol Ind Co Ltd Composition and aerosol composition for external skin preparation
US10073104B2 (en) 2013-03-14 2018-09-11 Siemens Healthcare Diagnostics Inc. Control of pH in aqueous urea-containing solutions utilizing amino acid-containing compositions
US10921333B2 (en) 2013-03-14 2021-02-16 Siemens Healthcare Diagnostics Inc. Control of pH in aqueous urea-containing solutions utilizing amino acid-containing compositions
US11921124B2 (en) 2013-03-14 2024-03-05 Siemens Healthcare Diagnostics Inc. Control of pH in aqueous urea-containing solutions utilizing amino acid-containing compositions
CN105439907A (en) * 2015-12-02 2016-03-30 锦西天然气化工有限责任公司 Production technology of stable urea
WO2020251017A1 (en) * 2019-06-14 2020-12-17 ゼリア新薬工業株式会社 Composition for external application

Also Published As

Publication number Publication date
JPH0456002B2 (en) 1992-09-07

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