JPS59196809A - Hair cosmetic composition - Google Patents
Hair cosmetic compositionInfo
- Publication number
- JPS59196809A JPS59196809A JP7119683A JP7119683A JPS59196809A JP S59196809 A JPS59196809 A JP S59196809A JP 7119683 A JP7119683 A JP 7119683A JP 7119683 A JP7119683 A JP 7119683A JP S59196809 A JPS59196809 A JP S59196809A
- Authority
- JP
- Japan
- Prior art keywords
- hair
- fatty acid
- ester
- mono
- amino acid
- 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
- 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
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/40—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
- A61K8/44—Aminocarboxylic acids or derivatives thereof, e.g. aminocarboxylic acids containing sulfur; Salts; Esters or N-acylated derivatives thereof
-
- 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
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/49—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds
- A61K8/4973—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with oxygen as the only hetero atom
-
- 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
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/60—Sugars; Derivatives thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q5/00—Preparations for care of the hair
- A61Q5/02—Preparations for cleaning the hair
-
- 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
- A61K2800/59—Mixtures
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Birds (AREA)
- Epidemiology (AREA)
- Cosmetics (AREA)
Abstract
Description
【発明の詳細な説明】 この発明は、毛髪化粧料組成物に関する。[Detailed description of the invention] The present invention relates to a hair cosmetic composition.
近年、毛髪はプラソ/ング、/′P−マ、ヘアカラー等
の普及により、非常にいたみ易い環境におかれている。In recent years, hair has become extremely susceptible to damage due to the spread of hair dyes, hair dyes, hair dyes, and the like.
消費者の声も、毛髪がパザパサして落ちつかないとか、
つやがないとか、ブラッシング性が悪いという悩みが実
に多い。従って、毛髪化粧料としては、毛髪をしっとり
と落ちつかせ、つや及びブラッシング性を向上させるも
のが望まれている。Consumers also say that their hair is dry and restless.
There are many problems with lack of shine and poor brushability. Therefore, hair cosmetics that moisturize and soothe hair and improve shine and brushability are desired.
また、毛髪は首筋等の肌に直接触れるものであり、また
手入れの際は必す手で触11られる部分であるから、べ
たべたした生い感触は徹鳳的に嫌われる。従って、べた
つきのない安定した乳化系であることも、好ましい毛髪
化粧料の条件である。Furthermore, since hair comes into direct contact with the skin of the nape of the neck and must be touched with hands when caring for it, a sticky, raw texture is strongly disliked. Therefore, a stable emulsion system without stickiness is also a desirable condition for hair cosmetics.
しかしながら、従来の毛髪化粧料には、「jl」記した
諸性能を全て兼ね佑Iえたものは見あたらない。すなわ
ち、従来の毛髪化粧料は多搦の油分を含むため、仕上り
が軍<、いつまでもべたべたし、ているものが多い。一
方、毛髪化粧料中の油分の配合嘔を少なくすることによ
って、軽くてサランとしたも髪の仕上り効果を得ること
が試みられているが、/1′81分ン′少なく1゛ると
べたつきは若干減少1゛るが、毛髪のつや及びブラッシ
ング性が著しく低下してしまう。However, among conventional hair cosmetics, there is no one that can satisfy all of the various properties listed in "jl". In other words, because conventional hair cosmetics contain oily components, many of them end up with a greasy, sticky finish. On the other hand, attempts have been made to reduce the amount of oil contained in hair cosmetics to achieve a light, saline-like finish to the hair, but if it is as low as 1'81' or 1', it becomes sticky. However, the gloss and brushability of the hair are significantly reduced.
この発明の目的は、毛髪をしっとりと落ちつかせ、グラ
ソシング性を向上させ、べたつきを少なくシ、かつ髪を
まとめ昌くすることができる分散安定性の良いグル状毛
髪化粧料組成物を提供することである。An object of the present invention is to provide a glue-like hair cosmetic composition with good dispersion stability that can moisturize hair, improve glossability, reduce stickiness, and make hair manageable. It is.
キルエステル塩と、0.7ないし5蒐量%の炭素数]4
7いL22の直鎖状飽和アルコールと。Kill ester salt and 0.7 to 5% carbon number]4
7 L22 linear saturated alcohol.
01ない1〜2重指%のソルビタン脂肪酸エステ九と、
0]すいし2車重%のポリグリセリン脂肪量コステルと
、05ないしl O軍V%の多価アルコール又はそのア
ルキレンオキシド付加誘壱体とを・含有するモ髪化粧享
」組成物を提供する。01% 1-2% sorbitan fatty acid esthetics nine,
To provide a hair make-up composition containing a polyglycerin fat content costel of 2% by weight and a polyhydric alcohol or an alkylene oxide addition derivative thereof of 05 to 10% by weight.
この発19]の組1戎物の第1の必須成分であるモノN
−長鎖アシル塩基性アミノ酸低級アルキルエステル塩を
構成する塩基性アミノ酸として。Mono N, which is the first essential component of set 1 of this expression 19]
- As a basic amino acid constituting a long-chain acyl basic amino acid lower alkyl ester salt.
例えばオルニテン、リジン及びアルギニン省の天然アミ
ノ酸を挙げることができる。また、例えはα、γ−V゛
アミノ酪酸のような合成アミノ酸も同様に用いることが
できる。これらは光学活性体でもラセミ体でもよい。Mention may be made, for example, of the natural amino acids of ornitene, lysine and arginine. Furthermore, synthetic amino acids such as α,γ-Vaminobutyric acid can be used as well. These may be optically active or racemic.
モノN−長鎖アシル塩基性アミノ酸低級アルキルエステ
ル塩を構成するアシル恭は、炭素数が8ないし22の飽
和又は不飽和の脂肪酸残基である。これらは天然のもの
でも合成されたものでもよい。例えはラワロイル基、ミ
リスチル基、バルミトイル基及びステアロイル基などの
ることかできる。The acyl constituting the mono N-long chain acyl basic amino acid lower alkyl ester salt is a saturated or unsaturated fatty acid residue having 8 to 22 carbon atoms. These may be natural or synthetic. Examples include lawaloyl group, myristyl group, valmitoyl group, and stearoyl group.
モノN−長鎖アシル塩基性低級アルキルエステル塩とし
ては、例えば塩酸塩若しくは&lt酸塩のような無機敏
塩、又は1例えば酢敵塩、酒石ia、り−cン酸塩%
p−トルエンスルホン醸颯。Mono N-long chain acyl basic lower alkyl ester salts include inorganic sensitive salts such as hydrochloride or <2<
p-Toluenesulfone brewed.
脂肪酸塩、電性アミノ岐塩、若[7くはピログルタミン
酸塩のような有機酸塩を採用することができる。こわら
のうち、塩酸塩及びL又はDL−ピロリドンカルざン酸
塩が好ましい。Organic acid salts such as fatty acid salts, electroconductive amino acid salts, and pyroglutamic acid salts can be employed. Among the stiff salts, hydrochloride and L- or DL-pyrrolidonecarzanate are preferred.
/
低級アルキルエステル部分としては、Vチルエステル、
エチルエステル、プロピルエステル、グチルエステル、
Kンテルエステル、ヘキシルエステル、ヘプチルエステ
ル及びオクチルニスデルが適当である。/ As the lower alkyl ester part, V thyl ester,
Ethyl ester, propyl ester, butyl ester,
Suitable are esters of potassium, hexyl esters, heptyl esters and octylnisder.
モノN−長鎖アシル塩基性アミノ酸低級アルキルエステ
ル塩の配合ff1tゴO工ないし5重量%である。The composition of the mono-N-long chain acyl basic amino acid lower alkyl ester salt is 5% by weight.
この発明の第2の必須成分である炭素数14ないL 2
2の直鎮状飽和アルコールは、上述の千)N−長鎖アシ
ル塩基性アミノ酸低級アルキルゴスデル塩と一対と71
って毛髪に吸ネ」され。L 2 having 14 carbon atoms, which is the second essential component of this invention
The linear saturated alcohol of No. 2 is paired with the above-mentioned 1,000) N-long chain acyl basic amino acid lower alkyl Gosdell salt and 71
"It's sucked into my hair."
’tf+にし髪の保水性を増大させて4s髪を落ちつか
せる。この飽和アルコールの炭素数か13以下でtt:
t: ;e *、を落ちつかせる効果が劣り、炭素数が
22を軸身ても毛髪の保水性が小さく、毛髪をikちつ
かせる効果が弱い。また、不飽和アルコールV、j1.
モノN−長鎖アシル塩基性アミノ酸低級ア/Lギルエス
テル塩と効率長く対を作らず。'tf+ increases hair's water retention and soothes 4S hair. If the number of carbon atoms in this saturated alcohol is 13 or less, tt:
t: ; e *, is poor in its calming effect, and even if the number of carbon atoms is 22, the water retention property of the hair is low, and the effect of making the hair ik is weak. Moreover, unsaturated alcohol V, j1.
Mono-N-long-chain acyl basic amino acid lower A/L-gyl ester salts and do not pair efficiently for a long time.
二(L髪に上述の性能を与えない。この飽和アルコール
の配合yは0.7ない〔−5車悌%である。2 (does not give the above-mentioned performance to L hair.The content of this saturated alcohol is 0.7% [-5%).
この発明の組成物が毛髪表面に均一に吸着され、かつ安
定な分散組成物として存在して商品価値を保持するため
には、上述の成分に加え、ソルビタン脂肪酸エステル、
ポリグリセリン脂肪酸エステル及び多(+Ijアルコー
ル又はそのアルキレンオキシド付加誘導体の3成分を含
有することが必須的である。In order for the composition of this invention to be uniformly adsorbed on the hair surface and to exist as a stable dispersion composition to maintain commercial value, in addition to the above-mentioned components, sorbitan fatty acid ester,
It is essential to contain three components: polyglycerol fatty acid ester and poly(+Ij alcohol or its alkylene oxide addition derivative).
この発明の組成物の第3の必須成分であるソルビタン脂
肪酸エステルを構成する脂肪駁は飽和脂肪酸、側鎖を何
する不飽和脂肪酸であ2)。The fats constituting the sorbitan fatty acid ester, which is the third essential component of the composition of the present invention, are saturated fatty acids and unsaturated fatty acids with different side chains2).
好ましい脂肪酸は、カプリル酸、カブリン酸。Preferred fatty acids are caprylic acid and capric acid.
シラリン酸、ミリステン酸、ノやルミナンm、ステアリ
ン酸、ベヘニン酸、オレイン酸、リノール?、’)/レ
ン飯、’)7ノールに、1ソステアリン酸、ウンデシレ
ン酸、ヒドロギシスデアリン酸、アビエチン賦、イソオ
クタン准、イソへせテ′カン龜、2−エチルー\キサr
カン峻及びジノリン脂肪rb、などておる。Sillaric acid, myristic acid, luminan m, stearic acid, behenic acid, oleic acid, linoleic acid? , ')/Length rice, ') 7-nol, 1 sostearic acid, undecylenic acid, hydroxydearic acid, abietin addition, isooctane, isohosete'kan, 2-ethyl\xar
Kanshun and Ginoline fat RB, etc.
ソルビタン脂肪酸エステルの誰合鍬は0.1ないし2重
址%である。The amount of sorbitan fatty acid ester is 0.1 to 2%.
この発明の組成物の第4の必須成分である7ノ?リグリ
セリン脂肪酸エステルのグリセリン部分はモノグリセリ
ン、ソグリセリン、トリグリセリン、テトラグリセリン
、ベン汐グリセリン、ベキザグリセリン。ノナグリセリ
ン、テトラグリセリン等である。7, which is the fourth essential ingredient of the composition of this invention. The glycerin part of liglycerin fatty acid ester is monoglycerin, soglycerin, triglycerin, tetraglycerin, benshio glycerin, and bexaglycerin. Nonaglycerin, tetraglycerin, etc.
ポリグリセリン脂肪酸エステルを構成する脂肪酸VCつ
いてり1.上述1.、たソルビlン脂肋敏エンゾルを構
成する脂肪酸と全く同様のことが言にる。Fatty acid VC constituting polyglycerin fatty acid ester 1. Above 1. The same thing can be said about the fatty acids that make up sorbitol.
、I? I) クリセリン脂肪酸エン、デルの配合量は
O]ηいり、 27Rh、i%である。,I? I) The blending amount of chrycerin fatty acid ene and del is O]η, 27Rh, i%.
との発明の第5の必須成分である多価アルコール又ン」
そのアルキレンオキシド付加誘導体(ただ11、ソルビ
タン脂肪酸ニスデル、ポリグリセリン1111肋fンエ
ステルを除く)の多価アルコ−A= ノ好yi: I−
い具体例とし−(、グリセリン、ポリグリセリン(ノグ
リセリン、 ト リグリセリン、テトラグリセリン、ペ
ンータグリ士リン、ヘキサグリセリン、オクメグリセリ
ン、ノナグリセリン、デカグリセリン痔−)、コニブー
レグリコール、ポリエチレングリコール(平均分子量2
00ないし600のものが好ましい)、プロピレングリ
コール、ポリプロピレングリコール(平均分子量20(
)ないし6 f) 0のものが好ま1.い)。Polyhydric alcohol which is the fifth essential ingredient of the invention of
Polyhydric alcohols of its alkylene oxide addition derivatives (excluding only 11, sorbitan fatty acid Nisder, polyglycerin 1111 ester): I-
Specific examples include glycerin, polyglycerin (noglycerin, triglycerin, tetraglycerin, pentaglycerin, hexaglycerin, ocumeglycerin, nonaglycerin, decaglycerin), coniboule glycol, polyethylene glycol (average Molecular weight 2
00 to 600 is preferred), propylene glycol, polypropylene glycol (average molecular weight 20 (preferably)
) to 6 f) 0 is preferred 1. stomach).
1.3−ブチレングリコール及びソルビトール等を挙げ
ることができる。Examples include 1,3-butylene glycol and sorbitol.
また5そのアルギレンオキシド(=J加誘導体として(
・ま、エチレンオキシド及びブ′ロビレンオキ/トイ・
[加誘?!1併が好まし、い。多価アルコールのアルキ
レンオキシド付加誘導体の好ましい具体例として、ポリ
オキシプロピレンソルビトール(平均分子量20()な
いし700のものが好ましい)、Iリオ千ジエチレンソ
ルビトール(平均分子4i’< 200ないし280
flのものが好ましい)及び号?リメキ/エナレンポリ
オキシプロピレンフルビトール(5]L均分子’% 3
00ないし2600のものが好ましい)支を挙げること
ができる。In addition, 5 its algylene oxide (=J derivative (
・Well, ethylene oxide and brobylene oxide/toy・
[Invitation? ! One combination is preferred. Preferred specific examples of alkylene oxide addition derivatives of polyhydric alcohols include polyoxypropylene sorbitol (preferably those with an average molecular weight of 20 ( ) to 700), Iliothousandiethylene sorbitol (average molecular weight 4i'< 200 to 280)
(preferably fl) and issue? Limeki/Enalene Polyoxypropylene Fulbitol (5) L equivalent molecular weight '% 3
00 to 2600 is preferred).
多価アルコール又はそのアルキレンオキシド付加誘導体
の配合量は05ないり、10重量%でを)る。The amount of the polyhydric alcohol or its alkylene oxide addition derivative is 0.5 to 10% by weight.
この発明の毛髪化粧料組成物は、ヘアローシ利ン、ヘア
コンディ/フナ−。ヘアリンス等の各種形眸で適用する
ことができる。The hair cosmetic composition of the present invention can be used as hair lotion, hair conditioner/funer. It can be applied in various forms such as a hair rinse.
明の効果ヲ7「λ一体的に示す。4例の説明に先立つ−
(1,−jlず4例で採用した試><、−、法eこつい
て説明する。The effect of light 7 "λ is shown in one piece. Prior to the explanation of the four examples -
(Tests adopted in 4 cases without 1, -jl><, -, method e I will explain in detail.
(1〕性能試験
量%のセナルアルコール、 10 止F、%のプロピレ
ングリコール及び86上鼠%の水から成る、従来からよ
く知られた代表的な汎用リンス組成物の性能を基準とし
た5段階評価でる)る。(1) Five levels based on the performance of a typical, well-known general-purpose rinse composition consisting of performance test amounts of 10% senal alcohol, 10% F, propylene glycol, and 86% water. Evaluation).
◎:良い
○:やや良い
Δ:同等
×;やや劣る
××:劣る
(2)性状試験
試料組成物を1(JOm/?のガラス容器に密封し、−
5”C,〜40℃、v′C6カカ保存し7た後の外観を
観察し、て、その分散女定性な評佃1した。◎: Good ○: Fairly good Δ: Equal
The appearance after storage at 5''C, ~40°C, and V'C6 temperature was observed, and the dispersion quality was evaluated as 1.
○:変化なし
Δ;油粕と水相が明らかに分離
試験例1
881表に示す組成を有する7神の試料組成物を調製し
、七の性能及び性状を評価(、た。結果を同表に示す。○: No change Δ: Oil cake and aqueous phase are clearly separated Test Example 1 Seven sample compositions having the compositions shown in Table 881 were prepared, and the performance and properties of seven were evaluated.The results are shown in the same table. show.
同表から明らかなように、モノN−長鎖アシル塩基性ア
ミノ酸低級アルキルエステル塩、飽和アルコール、ソル
ビ汐ンIJFi 肋hyニスデル、2式IJ グリセリ
ンカ旨肪酸エステル及び多(+lliアルコールのいず
′I]か1つが欠けても不発、明の効果を達成できない
ことかわかる。As is clear from the same table, mono N-long chain acyl basic amino acid lower alkyl ester salts, saturated alcohols, Sorbishio IJFi, Nisdel, Formula 2 IJ glycerin fatty acid esters, and poly(+lli alcohols) 'I] Even if one of them is missing, it can be seen that there is no invention, and the effect of light cannot be achieved.
実施例2〜5
第2表に示す組成を有する4種の毛髪化粧料糾暇物を1
7.i製L2.それらの性能及び性状を評価(−た。結
果を同表に示す。Examples 2 to 5 Four types of hair cosmetics having the compositions shown in Table 2 were mixed into one
7. Made by i L2. Their performance and properties were evaluated. The results are shown in the same table.
同表から明らかなように、炭素数が8ないし22の脂肪
酸残本を有するモノN−長鎖アシル塩基性アミノ酸低級
アルギルエステル塩を用いたときに、A)”=4明の効
果を達成できる。As is clear from the same table, when using a mono-N-long chain acyl basic amino acid lower argyl ester salt having a fatty acid residue having 8 to 22 carbon atoms, the effect of A)" = 4 brightness was achieved. can.
実施例6〜9
第3表にボす組成を有ず4)4(土の二り髪化粧料粘呆
を同表VC示す。Examples 6 to 9 The compositions shown in Table 3 are shown in Table 3.
同表より、炭素数14ないし220直妬飽和フルコール
を用いたときに、いす1しも本発明の効果を近1戊でき
ることがわかる。なお、炭素数かJ:3以十及023以
上のアルコ、−ル、又は不だ! イ4i−jルコールな
用いた場合νL(μ、本発明の効η得、J認めらり、な
いことかわかっている。From the same table, it can be seen that the effect of the present invention can be almost 100% achieved by using a straight saturated fluorocarbon having 14 to 220 carbon atoms. In addition, carbon number or J: 3 or more and 023 or more alcohol, -r, or not! A4i-j It is known that when alcohol is used, νL(μ, the effect η of the present invention, J is recognized, there is no effect).
実施例1O
第4表に示す組成を有するヘアl−IJ −)メント組
成物を調製し、その性能及び分散安定性を評価した。Example 1O A hair l-IJ-)ment composition having the composition shown in Table 4 was prepared and its performance and dispersion stability were evaluated.
第 4 表
このヘアトリートメント組成@は1毛髪に対して俊れた
まとまシ性、しつとシ感、グランシング性を示し、分散
安定性の良好なものでβっだ。Table 4 This hair treatment composition @ shows excellent cohesiveness, stiffness, and glancing properties for each hair, and has good dispersion stability, which is rated as β.
実施例11
第5表に示す組成を有するヘアローションボ1[成物を
調製し、その性能及び分散安T性をかi’ ([1+1
した。Example 11 Hair lotion 1 having the composition shown in Table 5 was prepared, and its performance and dispersion stability were evaluated.
did.
第 5 衣
このヘアローション組成物は、実施例10のヘアトリー
トメント♀口成物と同様、優れた性能)4シび分散安定
性を示[7た。No. 5 This hair lotion composition, like the hair treatment mouth composition of Example 10, exhibited excellent performance (4) and dispersion stability (7).
Claims (1)
22のモノN−長鎖アシル塩基性アミノ酸低級アルキ
ルエステル塩ト、0.7々いし5中片1%の炭素数14
ないし22の直鎖状飽和アル−y −/L/ 、!:、
0.1ないし2重量%のソルビタン脂肪酸エステルと、
0.工ないし21F量%のポリグリセン脂肪醒ニスデル
と、0.5ないし10車111%の多価アルコール又は
そのアルキレンオキンドイ・1加誘2行杯とを含有する
毛髪化粧料組成物。01 to 5% by weight, the number of carbon atoms in the acyl group is 8,
22 mono-N-long chain acyl basic amino acid lower alkyl ester salt, 0.7 to 5, 1% carbon number 14
to 22 linear saturated Al-y-/L/,! :,
0.1 to 2% by weight of sorbitan fatty acid ester;
0. A hair cosmetic composition containing 0.5 to 111% of a polyhydric alcohol or an alkylene alcohol thereof in an amount of 0.5 to 21% by weight of polyglycerol.
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP7119683A JPS59196809A (en) | 1983-04-22 | 1983-04-22 | Hair cosmetic composition |
GB08410237A GB2140297B (en) | 1983-04-22 | 1984-04-19 | Hair treatment compositions |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP7119683A JPS59196809A (en) | 1983-04-22 | 1983-04-22 | Hair cosmetic composition |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS59196809A true JPS59196809A (en) | 1984-11-08 |
JPS635006B2 JPS635006B2 (en) | 1988-02-01 |
Family
ID=13453669
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP7119683A Granted JPS59196809A (en) | 1983-04-22 | 1983-04-22 | Hair cosmetic composition |
Country Status (2)
Country | Link |
---|---|
JP (1) | JPS59196809A (en) |
GB (1) | GB2140297B (en) |
Families Citing this family (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH01242517A (en) * | 1988-03-25 | 1989-09-27 | Ajinomoto Co Inc | Hair cosmetic composition |
FR2649697A1 (en) * | 1989-07-11 | 1991-01-18 | Oreal | NOVEL URETHANNE DERIVATIVES, THEIR PREPARATION AND THEIR APPLICATION IN PARTICULAR AS MOISTURIZING AGENTS IN COSMETIC OR PHARMACEUTICAL COMPOSITIONS FOR THE TREATMENT OF DRY SKINS |
GB9222772D0 (en) * | 1992-10-30 | 1992-12-09 | Unilever Plc | Cosmetic composition |
DE4309390C2 (en) * | 1993-03-23 | 2003-06-18 | Goldschmidt Ag Th | Method for regulating the viscosity of emulsions |
ES2092958B1 (en) * | 1995-01-10 | 1997-08-01 | Miret Lab | PROCEDURE FOR THE SYNTHESIS OF CATIONIC SURFACES DERIVED FROM THE CONDENSATION OF FATTY ACIDS WITH ESTERIFIED BASIC CHARACTER AMINO ACIDS AND THEIR APPLICATION AS ANTIMICROBIAL AGENTS. |
FR2738483B1 (en) * | 1995-09-07 | 1997-10-10 | Sederma Sa | NOVEL COSMETIC COMPOSITIONS FOR THE TREATMENT OF HAIR CONTAINING SYNTHETIC LIPIDS |
TW553747B (en) | 1997-10-30 | 2003-09-21 | Ajinomoto Kk | Nonionic surfactant |
DE19835327A1 (en) * | 1998-08-05 | 2000-02-10 | Henkel Kgaa | Hair treatment products |
GB9909294D0 (en) * | 1999-04-22 | 1999-06-16 | Unilever Plc | Treating hair by targeting enzymes |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS57200307A (en) * | 1981-05-30 | 1982-12-08 | Lion Corp | Hair cosmetic |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB1015261A (en) * | 1960-11-18 | 1965-12-31 | Kenneth Richard Dutton | Compositions based on short-chain substituted fatty acid amides and on amine complexes thereof, and exhibiting activity against micro-organisms |
CH509267A (en) * | 1968-02-19 | 1971-06-30 | Goldschmidt Ag Th | Process for the preparation of mixtures of amino acid derivatives |
JPS5123395B2 (en) * | 1972-10-23 | 1976-07-16 | ||
GB1485694A (en) * | 1975-01-22 | 1977-09-14 | Ajinomoto Kk | Gelling agents |
GB2097256B (en) * | 1981-04-02 | 1985-05-30 | Morelle Jean V | Compositions containing n-butyryl alphaaminoacids |
-
1983
- 1983-04-22 JP JP7119683A patent/JPS59196809A/en active Granted
-
1984
- 1984-04-19 GB GB08410237A patent/GB2140297B/en not_active Expired
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS57200307A (en) * | 1981-05-30 | 1982-12-08 | Lion Corp | Hair cosmetic |
Also Published As
Publication number | Publication date |
---|---|
GB8410237D0 (en) | 1984-05-31 |
GB2140297B (en) | 1986-04-23 |
JPS635006B2 (en) | 1988-02-01 |
GB2140297A (en) | 1984-11-28 |
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