JPS62106007A - Hair cosmetic - Google Patents

Hair cosmetic

Info

Publication number
JPS62106007A
JPS62106007A JP24262385A JP24262385A JPS62106007A JP S62106007 A JPS62106007 A JP S62106007A JP 24262385 A JP24262385 A JP 24262385A JP 24262385 A JP24262385 A JP 24262385A JP S62106007 A JPS62106007 A JP S62106007A
Authority
JP
Japan
Prior art keywords
hair
fatty acid
hair cosmetic
temperature stability
branched alkyl
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.)
Pending
Application number
JP24262385A
Other languages
Japanese (ja)
Inventor
Shuji Iwao
岩尾 修司
Yoshibumi Yamagake
山懸 義文
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.)
Lion Corp
Original Assignee
Lion Corp
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 Lion Corp filed Critical Lion Corp
Priority to JP24262385A priority Critical patent/JPS62106007A/en
Publication of JPS62106007A publication Critical patent/JPS62106007A/en
Pending legal-status Critical Current

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics 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
    • A61K8/33Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • A61K8/39Derivatives containing from 2 to 10 oxyalkylene groups
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q5/00Preparations for care of the hair
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q5/00Preparations for care of the hair
    • A61Q5/04Preparations for permanent waving or straightening the hair
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q5/00Preparations for care of the hair
    • A61Q5/12Preparations containing hair conditioners

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)
  • Birds (AREA)
  • Epidemiology (AREA)
  • Emergency Medicine (AREA)
  • Cosmetics (AREA)

Abstract

PURPOSE:To obtain a hair cosmetic such as hair liquid, hair rinse, hair tonic, etc., having excellent low-temperature stability and effective to straighten hair curled in bed, by compounding specific amounts of a fatty acid alkylolamide and a polyoxyethylene branched alkyl ether to a hydrated ethanol. CONSTITUTION:The objective hair cosmetic can be produced by compounding hydrated ethanol with (A) 0.01-7(wt)%, preferably 0.05-3% fatty acid alkylolamide such as coconut oil fatty acid diethanolamide, myristic acid monoethanolamide, etc., based on the hair cosmetic and (B) 0.1-10%, preferably 0.3-5% polyoxyalkylene branched alkyl ether [preferably the compound of formula I (R1 and R2 are 4-18C alkyl; n is 5-150) or the compound of formula II (R1 and R2 are 4-22C alkyl; n is 5-150)].

Description

【発明の詳細な説明】 この発明は、低温安定性や寝癖の直し易さに慶しタ、い
わゆるヘアリキッド、ヘアリンスあるいはヘアトニック
のような毛髪化粧料に関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to hair cosmetics, such as so-called hair liquids, hair rinses, and hair tonics, which are characterized by low-temperature stability and ease of correcting sleeping habits.

従来、脂肪酸アルキロールアミドは毛髪シャンプー等の
発泡助剤として用いられている。また毛髪リンス剤にも
、これとカチオン界面活性剤とを組合せて使用されてい
るが、該リンス剤は低温安定性に欠け、また保存中に濁
りや沈澱を生ずる現象があった。それらの対策としては
、ポリオキシエチレン脂肪酸アルキロールアミドを用い
たり、アニオン界面活性剤と組合せ、或はエタノールを
増量することによって、低温安定性の増大化が試みられ
た。
Conventionally, fatty acid alkylolamides have been used as foaming aids in hair shampoos and the like. A combination of this and a cationic surfactant is also used in hair rinses, but these rinses lack low temperature stability and tend to become cloudy or precipitate during storage. As a countermeasure to these problems, attempts have been made to increase the low-temperature stability by using polyoxyethylene fatty acid alkylolamide, combining it with an anionic surfactant, or increasing the amount of ethanol.

しかしながら、アニオン界面活性剤は、皮!膚の刺激を
もたらす等の危険性が悪念され、ポリオキシエチレン脂
肪酸アルキロールアミドの使用はその効果が不十分であ
り、エタノールの増量によっては、低温安定比は図れる
が、寝癖の直し易さは改善されなかった。
However, anionic surfactants are skin! The use of polyoxyethylene fatty acid alkylolamide is considered to be dangerous due to skin irritation, and although the low temperature stability ratio can be achieved by increasing the amount of ethanol, it is difficult to correct sleeping habits. was not improved.

一方、ポリオキシエチレン分岐アルキルエーテルは、こ
れ全一般の化、を科として配合することは既に知られて
おり(侍1jri昭48−5942号、同52−250
38号、同51−79734号各公報参照)、またヘア
リンス剤でもこれを用いることによって髪の風合いを良
くする、ということが既に知られている。(特開昭59
−106412号公報参照。) この発明は、毛髪化粧料の低温安定性を良好にし、優れ
た寝癖直し易さを持つことを目的としてなされたもので
あって、脂肪酸アルキロールアミド全0.01ないし7
重量%、及びポリオキシエチレン分岐アルキルエーテル
Th 0.1ないし10重fiL%の両者を含水エタノ
ールに配合してなることをその特徴とする。
On the other hand, it is already known that polyoxyethylene branched alkyl ether can be blended as a general compound (Samurai 1 Jri No. 48-5942, No. 52-250).
No. 38 and No. 51-79734), and it is already known that the texture of hair can be improved by using it in hair rinses. (Unexamined Japanese Patent Publication No. 59
See Publication No.-106412. ) This invention was made for the purpose of improving the low-temperature stability of hair cosmetics and providing excellent ease of correcting sleeping habits, and the invention aims to improve the low-temperature stability of hair cosmetics and provide excellent ease of correcting sleep habits.
It is characterized by blending both 0.1% to 10% by weight of polyoxyethylene branched alkyl ether Th into aqueous ethanol.

この発明における脂肪酸アルキロールアミドとしては、
下記一般式に該当するものが使用される。
The fatty acid alkylolamide in this invention includes:
Those corresponding to the following general formula are used.

阻しRばC8〜2゜の脂肪酸残基、 R4はH又はC2〜5のアルキロール基、R2は02〜
5のアルキロール基。
R is a C8~2° fatty acid residue, R4 is H or a C2~5 alkylol group, and R2 is a C8~2° fatty acid residue.
5 alkylol group.

此処て於て、脂肪酸としては揶子油脂肪酸、ラウリンI
N % ミリスチン酸、オレイン酸、ステアリン酸、イ
ソステアリン酸、あるいはベヘニン酸が、またアルキロ
ールアミンとしてはジェタノールアミン、モノエタノー
ルアミン、あるい!−1,イソプロパツールアミン等が
挙げら九る。
In this case, the fatty acids include coconut oil fatty acid and laurin I.
N % Myristic acid, oleic acid, stearic acid, isostearic acid, or behenic acid, and as the alkylolamine, jetanolamine, monoethanolamine, or! -1, isopropanolamine, and the like.

具体的な化合物としては、揶子油脂肪酸ジェタノールア
ミド、ミリスチン酸モノエタノールアミド、或はラウリ
ン酸モノエタノールアミドが挙げられる。これらのアミ
ド類はせれぞれ単独で、または適宜に組合せてこれを用
いることができる。
Specific compounds include coconut oil fatty acid jetanolamide, myristic acid monoethanolamide, and lauric acid monoethanolamide. These amides can be used alone or in appropriate combinations.

この脂肪酸アルキロールアミドを毛髪化粧料に対して0
.01ないし7f量チの割合で配合する。好ましい配合
割合は0.05ないし3f量チである。7重量%を越え
るとべたつきが増加し、0゜01重量%未満で(は寝癖
直しの効果が見られなho 当するものが実用される。
This fatty acid alkylolamide is added to hair cosmetics without any
.. Blend in a proportion of 01 to 7f. The preferred blending ratio is 0.05 to 3f. If it exceeds 7% by weight, stickiness increases, and if it is less than 0.01% by weight, no effect on correcting sleeping habits can be seen.

但しR4,R2はC4〜18のアルキル基、n  = 
 5 〜150 1″2 世しR,、R2はC4〜22のアルキル基、n  = 
 5 〜150 此処において、分岐アルコールとしては2−へキシルデ
カノール、2−ペプチルウンデカノール、2−オクチル
ド′デカノールが挙げられる。
However, R4 and R2 are C4-18 alkyl groups, n =
5 to 150 1″2 R,, R2 is a C4-22 alkyl group, n =
5 to 150 Here, examples of the branched alcohol include 2-hexyldecanol, 2-peptylundecanol, and 2-octyldodecanol.

こレラの分岐アルコールにエチレンオキサイドを5ない
し150モル、好ましくは10ないし40モル付加重合
させた化合物である。
It is a compound obtained by addition-polymerizing 5 to 150 moles, preferably 10 to 40 moles of ethylene oxide to the branched alcohol of Cholera.

このポリオキシエチレン分岐アルキルエーテルを毛髪化
粧料に対して0.1ないし10重量%の割合で配合する
。好ましい配合割合は0.3ないし5重tチである。1
0重量%を越えるとべたつきが増し、0.1重量%未満
では低温安定性トシては、プロティンやケラチン加水分
解物、アミノ酸あるいはその誘導体、カチオン界面活性
剤、両性界面活性剤、アニオン界面活性剤、PVP 、
 PVP/VA共重合体、アクリル酸メタクリル酸エス
テル共重合体、カチオン化セルローズ等のノニオン性、
カチオン性、両性高分子化合物、ビタミン類、ビオチン
、紫外線吸収剤等種々の物質を用いることができる。
This polyoxyethylene branched alkyl ether is blended into the hair cosmetic in a proportion of 0.1 to 10% by weight. The preferred blending ratio is 0.3 to 5 times. 1
If it exceeds 0% by weight, stickiness will increase, and if it is less than 0.1% by weight, it will be low temperature stable. ,PVP,
Nonionic materials such as PVP/VA copolymer, acrylic acid methacrylate copolymer, and cationized cellulose,
Various substances such as cationic and amphoteric polymer compounds, vitamins, biotin, and ultraviolet absorbers can be used.

罎後に含水エタノールとしては、水/エタノールの重l
比が99/1ないし60/40の溶液であって、好まし
くはこの比が80/20ないし70/30のものである
。この比が60/40よシ低くなると、毛髪化粧料の寝
癖直しの効果が劣るようになる。
As water-containing ethanol after boiling, the weight of water/ethanol is 1
Solutions with a ratio of 99/1 to 60/40, preferably 80/20 to 70/30. When this ratio is lower than 60/40, the effect of hair cosmetics on correcting sleep habits becomes inferior.

以上に述べたような新規な配合物全毛髪化粧料として用
いると、該化粧料の低温安定性が良好で、また毛髪の寝
癖直しが著しく良好となる効果を有する。
When the novel formulation described above is used as a whole hair cosmetic, the cosmetic has good low-temperature stability and has the effect of significantly improving the straightening of the hair.

次に実施例について説明をする。これらの実施例におい
て、配合割合の頭は毛髪化粧料に対する重量%ヲ、かっ
こ内の数字はアルキレンオキサイドの付加モル数を、P
OPはポリオキシプロピレンを、POEはポリオキシエ
チレンを表す。
Next, an example will be explained. In these examples, the compounding ratio is the weight percent of the hair cosmetic, and the number in parentheses is the number of moles of alkylene oxide added.
OP represents polyoxypropylene, and POE represents polyoxyethylene.

実施例1−3、および比較例1−3 第1表に示すような組成の整髪料全それぞれ調整し、そ
の効果の評価全併せて第1表中に表記した。評価の方法
及び基準は次のとおりである。
Example 1-3 and Comparative Example 1-3 All hair styling products having the compositions shown in Table 1 were prepared, and their effects were evaluated.The results are also listed in Table 1. The evaluation method and criteria are as follows.

(1)  べたつき 長さ15Il−ffi、重量10.Fの毛束に試料0.
3.9を均一に塗布し、12時間経過ののち、ノ9ネル
6名にて無処理の毛束を対照として、下記評価基準に従
い評点数を付した。
(1) Sticky length 15Il-ffi, weight 10. Sample 0.
3.9 was applied uniformly, and after 12 hours had passed, scores were given by 6 No9ers using untreated hair strands as a control according to the following evaluation criteria.

5点 きわめて良好。5 points: Very good.

4〃 良好。4. Good.

3〃 同等。3 Equivalent.

2〃 やや劣る。2. Slightly inferior.

1〃 劣る。1 Inferior.

上記評点の平均値を下記基準により第1表に示した。The average values of the above scores are shown in Table 1 based on the following criteria.

◎: 5ないし4以上。◎: 5 or 4 or more.

○: 4未満ないし3゜ Δ: 3未膚ないし2゜ ×: 2未満ないし0゜ (2)安定キ ロ0ゴのガラス瓶に調整された整髪料を充填し、−5℃
の温度下でこれを保存して、その安定性を次のように評
価した。
○: less than 4 to 3° Δ: 3 unskinned to 2°
It was stored at a temperature of

○; 濁シや沈澱を全く認めなかったもの。○: No cloudiness or sediment was observed.

Δ: 濁りや沈澱をやや認めたもの。Δ: Slight turbidity and precipitation observed.

×: 濁りや沈澱をかなシ多く認めたもの。×: A significant amount of turbidity and precipitation was observed.

(3)  寝m iN I、の易しさ 長さ15の、重コ凌3yの毛束を水で濡らし、直径2.
5 crnのカーラーにこれを巻き付けて乾燥すること
により、該毛束にカールを施した。調髪料0.1gを核
毛束に均一に塗布したのちに、櫛通し全行なってカール
の取れ具合金寝S直しの易しさとして次のように評価し
た。
(3) Wet a 3-year-old bundle of hair with a length of 15 and a diameter of 2.
The hair bundle was curled by wrapping it around a 5 crn curler and drying it. After 0.1 g of the hair conditioner was evenly applied to the core hair bundle, the hair was combed through and the ease of straightening the curl was evaluated as follows.

カーラーを巻く前の毛束の長さ t。Length of hair before wrapping with curlers t.

櫛通し前の毛束の長さ     L1 櫛通し後の毛束の長さ     t。Length of hair before combing L1 Length of hair after combing t.

率チを測定し、下記評価基準に従って評価を記号化して
第1表に示した。
The rate was measured, and the evaluation was coded according to the following evaluation criteria and shown in Table 1.

○: 90%以上カールが取シ去られ、殆んど毛髪は直
、凍状となったもの。
○: More than 90% of the curls have been removed, and most of the hair is frozen.

Δ: 約50%のカールが取り去られたもの。Δ: Approximately 50% of curls have been removed.

×: 約20係以下のカールが取り去られたものO 実施例7 いわゆるヘアリキッドの例である。×: O where curls of about 20 curls or less have been removed Example 7 This is an example of so-called hair liquid.

材料の調合割合を次のようにした。The mixing ratio of the materials was as follows.

POP(55)POE(5)グリセリルエーテル   
   10・O%POP(12)グリセリルエーテル燐
酸        8・Oj耶壬子油脂肪酸ジェタノー
ルアミド      0.5POEI:(20)オクチ
ルドデカノール        1.0ん dt−偽一酢酸トコフエロール       0.01
ビタミン860.03 植物抽出エキス          0.1グルコン酸
クロルヘキシノン    0.05色素       
       微量エタノール           
  30.0精製水             50.
0常法により製造されたこのヘアリキッドは、低温安定
性、べたつきおよび寝郷直し易しさについて、実施例工
ないし3におけると同様に優れていることが確認された
POP (55) POE (5) Glyceryl ether
10.0% POP (12) Glyceryl ether phosphoric acid 8. Ojyamse oil fatty acid jetanolamide 0.5 POEI: (20) Octyldodecanol 1.0 dt-pseudomonoacetic acid tocopherol 0.01
Vitamin 860.03 Plant extract 0.1 Chlorhexinone gluconate 0.05 Pigment
trace amount of ethanol
30.0 Purified water 50.
It was confirmed that this hair liquid produced by the conventional method had the same excellent low-temperature stability, stickiness, and ease of fixing as in Examples 3 to 3.

実施例8 匹わゆるヘアリンスの例である。Example 8 This is an example of a so-called hair rinse.

材料の調合割合を次のようにした。The mixing ratio of the materials was as follows.

塩化ステアリルトリメチールアンモニウム    0.
2%N −部子油脂肪酸アシルーL−グルタミン酸モノ
トリエタノールアミン塩(アミソフトCT−12)  
0.1ステアリン酸モノエタノールアミド    0.
1カチオン化セルローズ        0.2poE
(40)へキシルデカノール         0.6
ポリエーテル変性シリコーン       0.1色素
                  微量エタノール
             10.0精製水     
         88.4常法により製造されたこの
ヘアリンスは、低温安定性、べたつきおよび寝S直しの
易しさてついて、実施例工ないし3におけると同様に優
れていることが確認された。
Stearyltrimethylammonium chloride 0.
2% N-seed oil fatty acid acyl-L-glutamic acid monotriethanolamine salt (Amisoft CT-12)
0.1 Stearic acid monoethanolamide 0.
Monocationized cellulose 0.2poE
(40) Hexyldecanol 0.6
Polyether modified silicone 0.1 Dye Trace amount of ethanol 10.0 Purified water
88.4 It was confirmed that this hair rinse produced by a conventional method was excellent in terms of low-temperature stability, stickiness, and ease of redressing, similar to those in Examples 3 to 3.

実施例9 いわゆるヘアトニックの例である。Example 9 This is an example of a so-called hair tonic.

材料の調合割合を次のようにした。The mixing ratio of the materials was as follows.

ニコチン酸ベンジル         0.003・t
−メントール          0.2ツメチルポリ
シロキサン      2.0POE(40)硬化ひま
し油          1・0ミリスチン酸ソエタノ
ールアミド     0.3POI(20)イソステア
リルエーテル    0.5ビタミンgo、o1 サリチル酸ソーダ         0.1ピロクトン
オーラミン        0.15紫外線吸収剤  
         微量色素            
    微量エタノール             2
0.0fi#製氷              75.
4常法によシ製遺されたこのヘアトニックは、低温安定
性、べたつきおよび寝癖直しの易しさについて、実施例
工ないし3におけると同様に浸れていることが確認され
た。
Benzyl nicotinate 0.003・t
- Menthol 0.2 Methylpolysiloxane 2.0 POE (40) Hydrogenated castor oil 1.0 Myristic acid soethanolamide 0.3 POI (20) Isostearyl ether 0.5 Vitamin GO, O1 Sodium salicylate 0.1 Piroctone auramine 0.15 UV absorber
trace pigment
Trace amount of ethanol 2
0.0fi #ice making 75.
4 It was confirmed that this hair tonic prepared by the conventional method had the same properties as in Examples 3 to 3 in terms of low-temperature stability, stickiness, and ease of adjustment.

昭和 年 月 日 6  特許庁長官 宇 賀 道 部   殿1、事件の
表示 特願昭60−242623号 2・発明の名称 毛髪化粧料 3、補正をする者 事件との関係特許出願人 (676)ライオン株式会社 4、代理人 6、補正の対象 明 細 書  、 ′□′1 7、補正の内容 明細書中、別紙の通り訂正を行い捷す。
Month, Day 6, 1939 Director General of the Patent Office Michibe Uga 1, Indication of the case, Patent Application No. 1988-242623 2, Name of the invention, hair cosmetics 3, Person making the amendment Patent applicant related to the case (676) Lion Co., Ltd. 4, Agent 6, Specification subject to amendment, '□'1 7. Corrections will be made in the detailed statement of the contents of the amendment as shown in the attached sheet and will be deleted.

訂   正   書 明細書中、下記の訂正を行います。Correction book The following corrections will be made to the statement.

と訂正する。I am corrected.

[2)10頁、第1表を別紙の通り訂正する。[2) Page 10, Table 1 is corrected as shown in the attached sheet.

(3)11頁、8行、rdl−d−酢酸トコフェロール
」をrdl−α−醋酸トコフェロール」と訂正する。
(3) Page 11, line 8, "rdl-d-tocopherol acetate" is corrected to "rdl-α-tocopherol acetate".

(41x2頁、 4行、r塩化ステアリルトリメテール
アンモニウム」を「塩化ステアリルトジメチルアンモニ
ウム」と訂正する。
(Page 41x2, line 4, r stearyltrimethylammonium chloride” is corrected to “stearyltodimethylammonium chloride”.

Claims (1)

【特許請求の範囲】[Claims] 脂肪酸アルキロールアミドを0.01ないし7重量%、
及びポリオキシエチレン分岐アルキルエーテルを0.1
ないし10重量%の両者を含水エタノールに配合してな
る毛髪化粧料。
0.01 to 7% by weight of fatty acid alkylolamide;
and polyoxyethylene branched alkyl ether at 0.1
A hair cosmetic comprising 10 to 10% by weight of both in aqueous ethanol.
JP24262385A 1985-10-31 1985-10-31 Hair cosmetic Pending JPS62106007A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP24262385A JPS62106007A (en) 1985-10-31 1985-10-31 Hair cosmetic

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP24262385A JPS62106007A (en) 1985-10-31 1985-10-31 Hair cosmetic

Publications (1)

Publication Number Publication Date
JPS62106007A true JPS62106007A (en) 1987-05-16

Family

ID=17091807

Family Applications (1)

Application Number Title Priority Date Filing Date
JP24262385A Pending JPS62106007A (en) 1985-10-31 1985-10-31 Hair cosmetic

Country Status (1)

Country Link
JP (1) JPS62106007A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2001226233A (en) * 2000-02-18 2001-08-21 Mandom Corp Hair cosmetic composition
JP2012087108A (en) * 2010-10-22 2012-05-10 Mandom Corp Cosmetic with retaining refreshing feeling

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2001226233A (en) * 2000-02-18 2001-08-21 Mandom Corp Hair cosmetic composition
JP2012087108A (en) * 2010-10-22 2012-05-10 Mandom Corp Cosmetic with retaining refreshing feeling

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