JPS5856399B2 - Novel shampoo composition - Google Patents

Novel shampoo composition

Info

Publication number
JPS5856399B2
JPS5856399B2 JP8901876A JP8901876A JPS5856399B2 JP S5856399 B2 JPS5856399 B2 JP S5856399B2 JP 8901876 A JP8901876 A JP 8901876A JP 8901876 A JP8901876 A JP 8901876A JP S5856399 B2 JPS5856399 B2 JP S5856399B2
Authority
JP
Japan
Prior art keywords
parts
weight
shampoo composition
acid
pyridylthio
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
Application number
JP8901876A
Other languages
Japanese (ja)
Other versions
JPS5314710A (en
Inventor
徹哉 長島
薫 野本
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.)
Kawaken Fine Chemicals Co Ltd
Original Assignee
Kawaken Fine Chemicals 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 Kawaken Fine Chemicals Co Ltd filed Critical Kawaken Fine Chemicals Co Ltd
Priority to JP8901876A priority Critical patent/JPS5856399B2/en
Publication of JPS5314710A publication Critical patent/JPS5314710A/en
Publication of JPS5856399B2 publication Critical patent/JPS5856399B2/en
Expired 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
    • A61K8/49Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds
    • A61K8/4906Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with one nitrogen as the only hetero atom
    • A61K8/4933Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with one nitrogen as the only hetero atom having sulfur as an exocyclic substituent, e.g. pyridinethione
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q5/00Preparations for care of the hair
    • A61Q5/006Antidandruff preparations
    • 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

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  • 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)

Description

【発明の詳細な説明】 本発明はふけ発生防止剤として有効なビス(2−ピリジ
ルチオ−1−オキサイド)亜鉛塩を安定に分散懸濁させ
たシャンプー組成物に関するものである。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a shampoo composition in which bis(2-pyridylthio-1-oxide) zinc salt, which is effective as a dandruff inhibitor, is stably dispersed and suspended.

ビス(2−ピリジルチオ−1−オキサイド)亜鉛塩はふ
け発生防止剤として有効なことは広く知られているが、
このものは粉末で分散し難い性質があり、シャンプー基
剤中に単に加えただけでは放置するとき沈降し安定な分
散系を得ることができない。
Although it is widely known that bis(2-pyridylthio-1-oxide) zinc salt is effective as an anti-dandruff agent,
This powder is difficult to disperse, and if it is simply added to the shampoo base, it will settle when left to stand, making it impossible to obtain a stable dispersion.

このため、このものを安定に分散させるためには分散剤
あるいは増粘剤を用いることが必要である。
Therefore, in order to stably disperse this material, it is necessary to use a dispersant or a thickener.

シャンプーに用いられ得る分散剤、増粘剤としてはビニ
ル系ポリマー、カルボキシメチルセルロース、アルギン
酸塩、カゼイン、ゼラチンなどがあるが、その分散効果
が不充分で使用に供し得ないものが多い。
Examples of dispersants and thickeners that can be used in shampoos include vinyl polymers, carboxymethylcellulose, alginates, casein, and gelatin, but many of them cannot be used because their dispersing effects are insufficient.

近時ビス(2−ピリジルチオ−1−オキサイド)亜鉛塩
を安定に分散させるのにポリアクリル酸系樹脂を用いる
方法が特公昭−49−49117号公報に開示されてい
る。
Recently, Japanese Patent Publication No. 49-49117 discloses a method using a polyacrylic acid resin to stably disperse bis(2-pyridylthio-1-oxide) zinc salt.

この方法はビス(2−ピリジルチオ−1−オキサイド)
亜鉛塩を良く分散させる優れた方法であるが、pH7前
後での使用に限定され、そのうえ増粘、泡安定効果のあ
る脂肪酸アルカノールアミドや風合い向上効果のあるN
−長鎖アシルアミノ酸アルカリ金属塩などを添加すると
安定性、粘度を低下させるのでこれらを使用することが
できない難点がある。
This method uses bis(2-pyridylthio-1-oxide)
This is an excellent method for dispersing zinc salts well, but its use is limited to around pH 7, and in addition fatty acid alkanolamide, which has a thickening and foam stabilizing effect, and N, which has a texture-improving effect, are
- Addition of long-chain acylamino acid alkali metal salts and the like reduces stability and viscosity, so there is a drawback that they cannot be used.

本発明の目的は使用し得るpH領域が広く、皮ふ面のp
Hに近い弱酸性においても分散が安定で長期保存に十分
たえ得るシャンプー組成物を提供するにある。
The purpose of the present invention is to have a wide usable pH range, and to
It is an object of the present invention to provide a shampoo composition that has stable dispersion even under weak acidity close to H and can be stored for a long period of time.

本発明の他の目的は風合い向上効果があるN長鎖アシル
アミノ酸塩の単独又は増粘効果、泡安定効果がある脂肪
酸アルカノールアミドを配合しても分散性の悪化や粘度
低下が生じない。
Another object of the present invention is that even when an N long-chain acylamino acid salt, which has a hand-improving effect, is used alone or a fatty acid alkanolamide, which has a thickening effect and a foam-stabilizing effect, is blended, the dispersibility does not deteriorate or the viscosity decreases.

シャンプー組成物を提供するにある。To provide a shampoo composition.

本発明はN−長鎖アシルアミノ酸アルカリ金属塩に分散
剤としてヒドロキシアルキルセルロース類を用いてビス
(2−ピリジルチオ−1−オキサイド)亜鉛塩を水に分
散懸濁させれば本発明の目的が遂行し得るとの知見に基
づくものである。
The objects of the present invention can be achieved by dispersing and suspending bis(2-pyridylthio-1-oxide) zinc salt in water using N-long chain acylamino acid alkali metal salt and hydroxyalkyl cellulose as a dispersant. This is based on the knowledge that it is possible.

本発明に用いるヒドロキシアルキルセルロース類にはヒ
ドロキシエチルセルロース、ヒドロキシプロピルセルロ
ース、ヒドロキシプロピルメチルセルロースなどのよう
なヒドロキシアルキルセルロースの単独又は二種以上の
混合物が挙げられる。
The hydroxyalkylcelluloses used in the present invention include hydroxyalkylcelluloses such as hydroxyethylcellulose, hydroxypropylcellulose, hydroxypropylmethylcellulose, etc. alone or in combination of two or more.

本発明に用いるN−長鎖アシルアミノ酸アルカリ金属塩
はN−長鎖アシル基が、ラウロイル、ミリストイル、バ
ルミトイル、ステアロイル、オレオイル、やし油脂肪酸
残基、牛脂脂肪酸残基のような炭素数8ないし18を主
体としたアシル基で、アミノ酸がザルコシン、N−メチ
ル−β−アラニン、グルタミン酸などの中性或は酸性ア
ミノ酸で、アルカリ金属がナトリウム又はカリウムであ
る。
The N-long chain acylamino acid alkali metal salt used in the present invention has an N-long chain acyl group having 8 carbon atoms such as lauroyl, myristoyl, balmitoyl, stearoyl, oleoyl, coconut oil fatty acid residue, tallow fatty acid residue. The amino acid is a neutral or acidic amino acid such as sarcosine, N-methyl-β-alanine, or glutamic acid, and the alkali metal is sodium or potassium.

このN−長鎖アシルアミノ酸アルカリ金属塩は単品でな
く二種以上の混合物も使用し得る。
These N-long chain acylamino acid alkali metal salts may be used not only singly but also as a mixture of two or more.

本発明に用いる脂肪酸アルカノールアミドは、ラウリン
酸、ミリスチン酸、パルミチン酸、ステアリン酸、オレ
イン酸、やし油脂肪酸など炭素数8ないし18の脂肪酸
を主体とする脂肪酸とモノエタノールアミン、ジェタノ
ールアミン、モノイソプロパツールアミン、ジイソプロ
パノ−ルア□ンなどのアルカノールアミンとを縮合させ
て得た構造を有する脂肪酸アルカノールアミドが挙げら
れる。
The fatty acid alkanolamide used in the present invention includes fatty acids mainly consisting of fatty acids having 8 to 18 carbon atoms such as lauric acid, myristic acid, palmitic acid, stearic acid, oleic acid, and coconut oil fatty acid, monoethanolamine, jetanolamine, Examples include fatty acid alkanolamides having a structure obtained by condensing with alkanolamines such as monoisopropanolamine and diisopropanolamine.

本発明品の標準的配合の割合は、ビス(2−ピリジルチ
オ−1−オキサイド)亜鉛塩0.1ないし3.0部(重
量比で示す。
The standard blending ratio of the product of the present invention is 0.1 to 3.0 parts (by weight) of bis(2-pyridylthio-1-oxide) zinc salt.

以下同じ)、N−長鎖アシルアミノ酸アルカリ金属塩1
0ないし30部、ヒドロキシアルキルセルロース類0.
1ないし5部、及び全体量を100重量部とする水から
なるもの及びこの組成物に脂肪酸アルカノ−ルア□ドを
15部以下添加したものである。
(same below), N-long chain acylamino acid alkali metal salt 1
0 to 30 parts, 0 to 30 parts of hydroxyalkyl cellulose.
1 to 5 parts of water to make a total amount of 100 parts by weight, and 15 parts or less of fatty acid alkanol □ are added to this composition.

さらに本発明品には必要に応じて、グリコール類、グリ
セリン、ソルビット、ピロリドンカルボン酸塩のような
湿潤剤や香料、色素などを添加することができる。
Furthermore, humectants such as glycols, glycerin, sorbitol, and pyrrolidone carboxylic acid salts, fragrances, pigments, and the like can be added to the products of the present invention, if necessary.

本発明品はN−長鎖アシルアミノ酸アルカリ金属塩ヲヘ
ースにしヒドロキシアルキルセルロースを分散剤として
ビス(2−ピリジルチオ−1−オキサイド)亜鉛塩を安
定に懸濁分散させたシャンプー組成物で、使用し得るp
H領域が広く、皮ふ面のpHに近い弱酸性においても分
散が安定で長期保存に充分たえ得るものである。
The product of the present invention is a shampoo composition in which bis(2-pyridylthio-1-oxide) zinc salt is stably suspended and dispersed in a base of N-long chain acylamino acid alkali metal salt and hydroxyalkylcellulose as a dispersant. p
It has a wide H range and is stable in dispersion even in weakly acidic conditions close to the pH of the skin, making it suitable for long-term storage.

さらに本発明品の大きな特徴は、風合い向上効果のある
N−長鎖アシルアミノ酸塩の単独または増粘効果、泡安
定効果のあるアルカノールアミドを配合しても分散性、
増粘性などの効果を減することなく使用できることであ
る。
Furthermore, the major feature of the product of the present invention is that even when N-long chain acylamino acid salts, which have a hand-improving effect, are used alone or are mixed with an alkanolamide, which has a thickening effect and a foam-stabilizing effect, the product has good dispersibility.
It can be used without reducing effects such as thickening properties.

このようなことは従来品では見られなかった優れたもの
である。
This is an excellent feature not seen in conventional products.

以下本発明を実施例について説明するが本発明はこれら
によって限定されるものではない。
The present invention will be described below with reference to Examples, but the present invention is not limited thereto.

以下本文中部とあるは特記しない限り重量部を示す。The text in the text below indicates parts by weight unless otherwise specified.

実施例 I N−ラウロイルザルコシンナトリウム(用研ファインケ
ミカル■製商品名ノイポンSLE、活性剤純分30%:
以下同じ)活性剤純分として15部、ビス(2−ピリジ
ルチオ−1−オキサイド)亜鉛塩1部、及びヒドロキシ
エチルセルロース()・−キュレス社製商品名ナトロゾ
ール250 HR以下同じ)0.7部に水を加え全体を
84部にし、均一に溶解、分散懸濁させ、クエン酸を加
えてpH7とし全量を100部としたシャンプー組成物
を得た。
Example I N-lauroyl sarcosine sodium (trade name: Neupon SLE, manufactured by Yoken Fine Chemicals, activator purity 30%:
Same below) 15 parts as pure activator, 1 part of bis(2-pyridylthio-1-oxide) zinc salt, and 0.7 parts of hydroxyethyl cellulose (trade name: Natrozol 250 HR manufactured by Cures), 0.7 parts of water was added to bring the total amount to 84 parts, uniformly dissolved, dispersed and suspended, and citric acid was added to adjust the pH to 7 to obtain a shampoo composition with a total amount of 100 parts.

このものの粘度をB型回転粘度計(■東京計器製)を用
いて25℃で測定したところ722cpであった。
The viscosity of this product was measured at 25° C. using a B-type rotational viscometer (manufactured by Tokyo Keiki Co., Ltd.) and found to be 722 cp.

さらにこの組成物を50℃の恒温槽中で15日間放置し
て分散の安定性を測定したが、安定であった。
Further, this composition was left in a constant temperature bath at 50° C. for 15 days to measure the stability of the dispersion, and it was found to be stable.

実施例2〜3、比較例1〜7 実施例2〜3の場合にはN−ラウロイルザルコシンナト
リウム、N−ラウロイル−N−メチルβ−アラニンナト
リウム、N−ラウロイルグルタミン酸ナトリウム及びナ
トリウムラウリルエトキシ化サルフェートの界面活性剤
をいずれも活性剤純分として各15部及びヒドロキシエ
チルセルロース0.7部と、比較例としては前記界面活
性剤とヒドロキシエチルセルロースの代りに用いたポリ
アクリル酸(グツドリッチ社製商品名カーボポール94
1以下同じ)027部とでビス(2−ピリジルチオ−1
−オキサイド)亜鉛塩1部を実施例1に準じて水に溶解
分散懸濁しpH7とし全量を100部としてシャンプー
組成物を得た。
Examples 2 to 3, Comparative Examples 1 to 7 In the case of Examples 2 to 3, sodium N-lauroyl sarcosine, sodium N-lauroyl-N-methyl β-alanine, sodium N-lauroyl glutamate, and sodium lauryl ethoxylated sulfate 15 parts each and 0.7 parts of hydroxyethyl cellulose as pure surfactants, and as a comparative example, polyacrylic acid (trade name: Carbo, manufactured by Gutdrich) used in place of the above surfactant and hydroxyethyl cellulose. paul 94
027 parts of bis(2-pyridylthio-1)
- Oxide) 1 part of zinc salt was dissolved and dispersed in water according to Example 1, the pH was adjusted to 7, and the total amount was adjusted to 100 parts to obtain a shampoo composition.

ただしシャンプー組成物のpHが7以下の場合は水酸化
ナトリウム水溶液で、7以上の場合はクエン酸水溶液で
中和調整した。
However, if the pH of the shampoo composition was 7 or less, it was neutralized with an aqueous sodium hydroxide solution, and if it was 7 or more, it was neutralized with an aqueous citric acid solution.

これらの組成物の粘度及び分散安定性は、実施例1に準
じて測定し得られた結果を第1表に示す。
The viscosity and dispersion stability of these compositions were measured according to Example 1, and the results are shown in Table 1.

第1表の界面活性剤の銘柄の右端の数字はそれぞれ下記
の製品を用いたことを示す。
The numbers on the far right of the surfactant brands in Table 1 indicate that the following products were used.

(1):用研ファインケミカル■製活性剤純分り0%商
品名アラノンALE (2) : 味の素■製商品名アミソフ1−LS−11
(3):新日本理化■製活性剤純分30%、商品名ジノ
リン5PE (4):新日本理化株製活性剤純分30%、商品名ジノ
リンSP 第1表の結果から明らかなように、ヒドロキシエチルセ
ルロースを添加した系ではNISアシルアミノ酸塩配合
の場合は粘度が高く分散が安定であるのに比べ、高級ア
ルコールサルフェート及び高級アルコールエトキシ化サ
ルフェートの場合は低く分散も不安定であった。
(1): Manufactured by Yoken Fine Chemical ■ Activator purity 0% Product name: Alanone ALE (2): Manufactured by Ajinomoto ■ Product name: Amisof 1-LS-11
(3): 30% pure activator made by Shin Nippon Rika, trade name Ginoline 5PE (4): 30% pure activator made by Shin Nippon Rika, trade name Ginoline SP As is clear from the results in Table 1. In the system to which hydroxyethyl cellulose was added, the viscosity was high and the dispersion was stable in the case of NIS acylamino acid salt formulation, whereas the viscosity was low and the dispersion was unstable in the case of higher alcohol sulfate and higher alcohol ethoxylated sulfate.

またカーボポール941を添加した系では、いずれの活
性剤も低粘度で分散不安定であった。
In addition, in the system in which Carbopol 941 was added, all active agents had low viscosity and unstable dispersion.

実施例4〜6、比較例8〜1O N−ラウロイルザルコシンナトリウムを活性剤純分とし
て15部、ビス(2−ピリジルチオ−1オキサイド)亜
鉛塩1.0部、第2表に示される添加量のラウリン酸ジ
ェタノールアミド(用研ファインケミカル■製商品名ア
ミゾールLDE以下同じ)分散剤としてヒドロキシエチ
ルセルロース0.7部、比較例の場合はこれと同量のポ
リアクリル酸系樹脂0.7部とをバランス量の水を用い
て実施例1に準じて処理し全量を100部とした。
Examples 4 to 6, Comparative Examples 8 to 1O 15 parts of N-lauroylsarcosinate sodium as pure activator, 1.0 part of bis(2-pyridylthio-1 oxide) zinc salt, amount added as shown in Table 2 Lauric acid jetanolamide (trade name: Amizol LDE manufactured by Yoken Fine Chemicals ■) 0.7 parts of hydroxyethyl cellulose as a dispersant, and in the case of a comparative example, the same amount of polyacrylic acid resin 0.7 parts. It was treated according to Example 1 using a balanced amount of water to make the total amount 100 parts.

ただしpH調整は7以下の場合は水酸化ナトリウム水溶
液で、7以上の場合はクエン酸で中和調整した。
However, the pH was adjusted using an aqueous sodium hydroxide solution if the pH was 7 or less, and by citric acid if the pH was 7 or higher.

得られたこれらのシャンプー組成物の粘度及び分散安定
性を実施例1に準じて測定した。
The viscosity and dispersion stability of these shampoo compositions obtained were measured according to Example 1.

その結果を第2表に示す。The results are shown in Table 2.

第2表から明らかなようにN−ラウロイルザルコシンナ
トリウムとラウリン酸ジエタノールアミド系のシャンプ
ー組成物においてヒドロキシエチルセルロースを添加シ
タ。
As is clear from Table 2, hydroxyethylcellulose was added to the shampoo composition based on N-lauroylsarcosine sodium and lauric acid diethanolamide.

実施例面では増粘し、さらに分散が安定したのに対し、
ポリアクリル酸系樹脂を添加した比較側面は逆に粘度が
低下し分散が不安定になった。
In contrast to the examples, the viscosity increased and the dispersion became more stable.
On the contrary, the viscosity decreased and the dispersion became unstable in the comparison side in which polyacrylic acid resin was added.

さらに下記の実施例に示すように各種の長鎖アシルアミ
ノ酸アルカリ金属塩、ヒドロキシアルキルセルロース類
及び他の添加剤を配合したシャンプー組成物を調整しそ
の特性を観察した。
Furthermore, as shown in the Examples below, shampoo compositions containing various long-chain acylamino acid alkali metal salts, hydroxyalkyl celluloses, and other additives were prepared and their properties were observed.

下記実施例中の界面活性剤の右端の数字はそれぞれ下記
の市販品を用いたことを示す。
The numbers on the right end of the surfactants in the Examples below indicate that the following commercial products were used.

Claims (1)

【特許請求の範囲】 1 N−長鎖アシルアミノ酸アルカリ金属塩10ないし
30重量部とヒドロキシアルキルセルロース類0.1な
いし5重量部を用いてビス(2−ピリジルチオ−1−オ
キサイド)亜鉛塩0.1ないし3.0重量部を全体量が
100重量部とする水に分散懸濁してなるシャンプー組
成物。 2、特許請求の範囲第1項においてヒドロキシアルキル
セルロース類カヒドロキシエチルセルロース、ヒドロキ
シフロピルセルロース、ヒドロキシプロピルメチルセル
ロースのうち少くとも一種以上であるシャンプー組成物
。 3 N−長鎖アシルアミノ酸アルカリ金属塩10ないし
30重量部、ヒドロキシアルキルセルロース類0.1な
いし5重量部及び脂肪酸アルカノ−ルア□ド15重量部
以下を用いてビス(2−ピリジルチオ−1−オキサイド
)亜鉛塩0.1ないし3.0重量部を全体量が100重
量部とする水に分散懸濁してなるシャンプー組成物。 4 特許請求の範囲第3項においてヒドロキシアルキル
セルロース類カ、ヒドロキシエチルセルロース、ヒドロ
キシフロピルセルロース、ヒドロキシプロピルメチルセ
ルロースのうち少くとモ一種以上であるシャンプー組成
物。
[Scope of Claims] 1. Bis(2-pyridylthio-1-oxide) zinc salt is prepared by using 10 to 30 parts by weight of N-long chain acylamino acid alkali metal salt and 0.1 to 5 parts by weight of hydroxyalkyl cellulose. A shampoo composition prepared by dispersing and suspending 1 to 3.0 parts by weight in water in a total amount of 100 parts by weight. 2. A shampoo composition according to claim 1, which is at least one of the hydroxyalkylcelluloses hydroxyethylcellulose, hydroxyfuropylcellulose, and hydroxypropylmethylcellulose. 3 Bis(2-pyridylthio-1-oxide) using 10 to 30 parts by weight of N-long chain acylamino acid alkali metal salt, 0.1 to 5 parts by weight of hydroxyalkyl cellulose, and 15 parts by weight or less of fatty acid alkanol acid. ) A shampoo composition prepared by dispersing and suspending 0.1 to 3.0 parts by weight of a zinc salt in water in a total amount of 100 parts by weight. 4. A shampoo composition according to claim 3, which is at least one of hydroxyalkylcelluloses, hydroxyethylcellulose, hydroxyfuropylcellulose, and hydroxypropylmethylcellulose.
JP8901876A 1976-07-28 1976-07-28 Novel shampoo composition Expired JPS5856399B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP8901876A JPS5856399B2 (en) 1976-07-28 1976-07-28 Novel shampoo composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP8901876A JPS5856399B2 (en) 1976-07-28 1976-07-28 Novel shampoo composition

Publications (2)

Publication Number Publication Date
JPS5314710A JPS5314710A (en) 1978-02-09
JPS5856399B2 true JPS5856399B2 (en) 1983-12-14

Family

ID=13959156

Family Applications (1)

Application Number Title Priority Date Filing Date
JP8901876A Expired JPS5856399B2 (en) 1976-07-28 1976-07-28 Novel shampoo composition

Country Status (1)

Country Link
JP (1) JPS5856399B2 (en)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS57209210A (en) * 1981-06-18 1982-12-22 Shiseido Co Ltd Solubilization of bis (2-pyridylthio-1-oxide) zinc
JPS57209211A (en) * 1981-06-18 1982-12-22 Shiseido Co Ltd Antimicrobial composition
JPS59108707A (en) * 1982-12-14 1984-06-23 Lion Corp Cosmetic
WO2014128922A1 (en) * 2013-02-22 2014-08-28 株式会社コーセー Viscous detergent composition

Also Published As

Publication number Publication date
JPS5314710A (en) 1978-02-09

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