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JPS584003B2 - Seihatsuriyo - Google Patents
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JPS584003B2 - Seihatsuriyo - Google Patents

Seihatsuriyo

Info

Publication number
JPS584003B2
JPS584003B2 JP15184475A JP15184475A JPS584003B2 JP S584003 B2 JPS584003 B2 JP S584003B2 JP 15184475 A JP15184475 A JP 15184475A JP 15184475 A JP15184475 A JP 15184475A JP S584003 B2 JPS584003 B2 JP S584003B2
Authority
JP
Japan
Prior art keywords
celluloid
hair
hair styling
sample
water
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
JP15184475A
Other languages
Japanese (ja)
Other versions
JPS5276443A (en
Inventor
秋本新一
杉中昭典
藤井正彦
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.)
NOF Corp
Original Assignee
Nippon Oil and Fats 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 Nippon Oil and Fats Co Ltd filed Critical Nippon Oil and Fats Co Ltd
Priority to JP15184475A priority Critical patent/JPS584003B2/en
Publication of JPS5276443A publication Critical patent/JPS5276443A/en
Publication of JPS584003B2 publication Critical patent/JPS584003B2/en
Expired legal-status Critical Current

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  • Cosmetics (AREA)
  • Polyethers (AREA)

Description

【発明の詳細な説明】 本発明は整髪料に関し、特にセルロイドの侵食とカラー
シャツの汚染のない整髪料に関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a hair styling product, and more particularly to a hair styling product that is free from celluloid erosion and color shirt staining.

整髪料にはポマードやチックのようにゲル状のもの、ヘ
ヤークリームのようにエマルジョンのもの、あるいはへ
ヤーリキッドと称される透明液状のものなどさまざまな
タイプがあるが、扱いやすさ、洗髪のしやすさなどの理
由から、透明液状タイプの整髪料が広く使用されている
There are various types of hair conditioners, including gel-like products such as pomade and tic, emulsion products such as hair cream, and transparent liquid products called hair liquids. Transparent liquid type hair conditioners are widely used for reasons such as ease of application.

この透明液状整髪料は油溶性もしくは水に難溶性のポリ
アルキレングリコール誘導体をエタノール水溶液に溶解
したもので、ポリプロピレングリコール、ポリプロピレ
ングリコールモノブチルエーテルあるいはこれらのリン
酸エステル塩などが約20%、エタノール約60%、水
約20%、さらに香料、着色剤などが少量含有されてい
るのが一般的である。
This transparent liquid hair styling product is made by dissolving an oil-soluble or poorly water-soluble polyalkylene glycol derivative in an aqueous ethanol solution, and contains approximately 20% polypropylene glycol, polypropylene glycol monobutyl ether, or their phosphate ester salts, and approximately 60% ethanol. %, about 20% water, and typically contains small amounts of fragrances, coloring agents, etc.

この整髪料には従来から眼鏡のつるのセルロイドの侵食
問題があり、さらに最近流行しているカラーシャツにし
ろがついて洗たくしても落ちないという苦情が出ている
This hair styling product has long had the problem of erosion of the celluloid on the temples of glasses, and there have also been complaints that color shirts, which have become popular recently, have a fringe that does not come off even when washed.

セルロイドの侵食については、液体整髪料に使用するエ
タノールに強い侵食性があり、またベースとなるポリア
ルキレングリコール誘導体が侵食を示す場合も多い。
Regarding the erosion of celluloid, the ethanol used in liquid hair styling products has strong corrosive properties, and the base polyalkylene glycol derivatives often exhibit erosion.

前述のポリグロピレングリコールモノブチルエーテルに
はセルロイドの侵食性はないが、化合物がきわめて水に
溶けにくく、透明溶液にするには高濃度のエタノール水
溶液が必要となり、そのためにセルロイドが侵食される
と考えられる。
Although the aforementioned polyglopylene glycol monobutyl ether does not have the properties of corroding celluloid, the compound is extremely difficult to dissolve in water, and a highly concentrated ethanol aqueous solution is required to make a clear solution, which is thought to corrode celluloid. It will be done.

ポリグロピレングリコールモノブチルエーテルのリン酸
エステルはこの点を改良スるために開発されたものであ
るが、整髪力の良い高粘度品ではほとんど水溶性は改善
されない。
Phosphate ester of polyglopylene glycol monobutyl ether was developed to improve this problem, but high viscosity products with good hair styling properties hardly improve water solubility.

カラーシャツ汚染の原因は、不揮発分であるポリアルキ
レングリコール誘導体が水と親和性がないために織物上
に付着したまま残ることが原因と考えられる。
The cause of color shirt staining is thought to be that polyalkylene glycol derivatives, which are non-volatile components, have no affinity with water and therefore remain attached to the fabric.

一般に、炭素数3以上のアルキレンオキシドの重合体は
油溶性であり、炭素数2のエチレンオキシドの重合体は
水溶性であり、両者の共重合体はその比率により溶解性
が変わる。
Generally, a polymer of alkylene oxide having 3 or more carbon atoms is oil-soluble, a polymer of ethylene oxide having 2 carbon atoms is water-soluble, and the solubility of a copolymer of the two changes depending on the ratio thereof.

セルロイドの侵食をおこさない点では油溶性の化合物が
好ましく、カラーシャツを汚染しない点では水溶性の化
合物が好ましく、互に相反する性質を満足させる必要が
ある。
Oil-soluble compounds are preferred from the standpoint of not causing celluloid erosion, and water-soluble compounds are preferred from the standpoint of not staining the collar shirt, and it is necessary to satisfy contradictory properties.

この問題を解決するためにポリアルキレングリコールを
リン酸エステル化する方法や可溶化剤として非イオン界
面活性剤を配合する方法が試みられているが満足すべき
結果は得られず、セルロイドを侵食せず、カラーシャツ
を汚染せず、しかも従来品と同様に整髪力の良い新しい
整髪料用原料が要望されていた。
To solve this problem, attempts have been made to convert polyalkylene glycol into a phosphate ester and to incorporate nonionic surfactants as solubilizers, but satisfactory results have not been obtained. There was a need for a new raw material for hair styling products that would not contaminate colored shirts and have the same hair styling properties as conventional products.

本発明者らは鋭意研究の結果、1価の脂肪族アルコール
に親油性のアルキレンオキシドと親水性のエチレンオキ
シドとを付加重合させた化合物で、しかも全体の平均分
子量とエチレンオキシドの付加重合数とが一定の範囲に
ある化合物が整髪料用原料として優れていることを見出
した。
As a result of intensive research, the present inventors found that the compound is an addition polymerized monohydric aliphatic alcohol, lipophilic alkylene oxide, and hydrophilic ethylene oxide, and the overall average molecular weight and number of addition polymerizations of ethylene oxide are constant. It has been found that compounds within the range of 1 are excellent as raw materials for hair styling products.

すなわち、本発明はつぎの一般式 AO(RO)a(C2H4O)bH (ただし、Aは炭素数1〜22の脂肪族炭化水素基、R
は炭素数3〜18のアルキレン基、aはROで示される
アルキレンオキシドの重合数で全体の平均分子量が50
0〜5000になる整数、bはエチレンオキシドの重合
数で全体の平均分子量の3〜20重量%に相当する整数
That is, the present invention is based on the following general formula AO(RO)a(C2H4O)bH (where A is an aliphatic hydrocarbon group having 1 to 22 carbon atoms, R
is an alkylene group having 3 to 18 carbon atoms, a is the polymerization number of alkylene oxide represented by RO, and the overall average molecular weight is 50
An integer ranging from 0 to 5,000; b is an integer corresponding to the polymerization number of ethylene oxide, which corresponds to 3 to 20% by weight of the overall average molecular weight;

)で示される化合物の1種または2種以上の混合物を含
有する整髪料に関するものである。
) This relates to a hair styling product containing one or a mixture of two or more of the compounds shown in the following.

本発明に用いる化合物の原料アルコールとしては、直鎖
または側鎖の、飽和または不飽和の脂肪族アルコール、
たとえばメタノール、エタノール、n−ブタノール、カ
プリルアルコール、ラウリルアルコール、セチルアルコ
ール、ステアリルアルコール、オレイルアルコール、2
−エチルヘキサノール、インステアリルアルコール、オ
キソ法合成アルコール、ヤシ油還元アルコール、牛脂還
元アルコール等があり、これらのうち特に炭素数8〜2
2の飽和または不飽和の直鎖アルコールが望ましい。
The raw material alcohol for the compound used in the present invention includes linear or side chain saturated or unsaturated aliphatic alcohols,
For example, methanol, ethanol, n-butanol, caprylic alcohol, lauryl alcohol, cetyl alcohol, stearyl alcohol, oleyl alcohol,
- Ethylhexanol, instearyl alcohol, oxo-synthesized alcohol, coconut oil reduced alcohol, beef tallow reduced alcohol, etc. Among these, especially carbon number 8-2
2 saturated or unsaturated straight chain alcohols are preferred.

油溶性を示すアルキレンオキシドとしては、プロピレン
オキシド、プチレンオキシド、インブチレンオキシド、
テトラヒドロフラン、炭素数12〜18のα−オレフイ
ンオキシドなどの単独または混合物が用いられる。
Examples of oil-soluble alkylene oxides include propylene oxide, butylene oxide, inbutylene oxide,
Tetrahydrofuran, α-olefin oxide having 12 to 18 carbon atoms, and the like may be used alone or in mixtures.

エチレンオキシドの付加量が限定されるのは、・3重量
%以下ではカラーシャツの汚染がおこり、20重量%以
上ではセルロイドの侵食がおこるからである。
The amount of ethylene oxide added is limited because if it is less than 3% by weight, staining of the collar shirt will occur, and if it is more than 20% by weight, celluloid will be eroded.

また全体の平均分子量が500以下ではセルロイドの侵
食は避けられず、5000以上では合成が困難であり、
しかも除去困難なセルロイドを侵食する副生物が生成し
て好ましくない。
Furthermore, if the overall average molecular weight is less than 500, celluloid erosion is unavoidable, and if it is more than 5000, synthesis is difficult.
Moreover, by-products are produced that corrode the celluloid and are difficult to remove, which is undesirable.

本発明における油溶性のアルキレンオキシドと水溶性の
エチレンオキシドの結合位置は特に問題とはならないが
、好ましいのは油溶性のアルキレンオキシドを付加させ
た後にエチレンオキシドを付加させたブロック共重合物
である。
Although the bonding position of oil-soluble alkylene oxide and water-soluble ethylene oxide in the present invention is not a particular problem, preferred is a block copolymer in which ethylene oxide is added after adding oil-soluble alkylene oxide.

本発明に用いる化合物の整髪料としての用途はきわめて
広く、ヘヤーリキッドのほかにヘヤークリーム、ポマー
ド、チンクなどの基材としての使用も可能であり、セル
ロイドの侵食とカラーシャツの汚染のない整髪料が得ら
れる。
The compound used in the present invention has a very wide range of uses as a hair styling product, and in addition to hair liquid, it can also be used as a base material for hair creams, pomades, tinctures, etc., and is a hair styling product that does not erode celluloid or stain colored shirts. is obtained.

特に従来のへヤークリームは流動パラフィン等の鉱物油
を主体とするものが多くてエタノール主体のヘヤートニ
ックとはなじまなかったが、本発明に用いる化合物の使
用によりヘヤートニックとよくなじむヘヤークリームの
製造が可能である。
In particular, many conventional hair creams are mainly based on mineral oils such as liquid paraffin and are not compatible with hair tonics, which are mainly ethanol.However, by using the compound used in the present invention, a hair cream that is compatible with hair tonics can be produced. is possible.

つぎに本発明に用いる化合物の製造例を示す。Next, production examples of compounds used in the present invention will be shown.

製造例 1 内容積5lのオートクレープにセチルアルコール242
グと触媒としてカセイソーダ9gをとり、窒素ガス置換
後、100〜150℃、1.0〜7.0kg/cm2の
圧力下で、プロピレンオキシド1500gを付加させた
後、エチレンオキシド140gを付加させた。
Production example 1 242 cetyl alcohol in an autoclave with an internal volume of 5 liters
After replacing the mixture with nitrogen gas, 1500 g of propylene oxide was added thereto under a pressure of 1.0 to 7.0 kg/cm2, and then 140 g of ethylene oxide was added thereto.

リン酸を加えて触媒を中和し、生成した結晶を沢別して C16H33O(C3H6O)25(C2H4O)3H
に相当する化合物(試料A6)を1850g得た。
Neutralize the catalyst by adding phosphoric acid, and separate the formed crystals to obtain C16H33O(C3H6O)25(C2H4O)3H
1850g of a compound (sample A6) corresponding to the above was obtained.

製造例 2 製造例1と同様な条件で、n−ブタノール74グにエチ
レンオキシドを140g、つぎにプロピレンオキシドを
1500g付加させて1650gのC4H9O(C2H
4O)3(C3H6O)25Hに相当する化合物(試料
No2)を得た。
Production Example 2 Under the same conditions as Production Example 1, 140 g of ethylene oxide and then 1500 g of propylene oxide were added to 74 g of n-butanol to produce 1650 g of C4H9O (C2H
A compound (sample No. 2) corresponding to 4O)3(C3H6O)25H was obtained.

製造例 3 製造例1と同様な条件で、n−ブタノール74gにプロ
ピレンオキシド1500gとエチレンオキシド140g
との混合物を付加させて、1650gのC4H9O{(
C3H6O)25(C2H40)3)Hに相当するラン
ダム共重合物(試料屑3)を得た。
Production Example 3 Under the same conditions as Production Example 1, 1500 g of propylene oxide and 140 g of ethylene oxide were added to 74 g of n-butanol.
1650 g of C4H9O{(
A random copolymer (sample scrap 3) corresponding to C3H6O)25(C2H40)3)H was obtained.

以下同様にして、表1の化合物を得た。The compounds shown in Table 1 were obtained in the same manner.

得られた化合物9種と従来用いられてきた化合物6種に
ついて、セルロイドの侵食性とカラニシャツ汚染性に関
する基礎的な試験結果を表1に示す。
Table 1 shows basic test results regarding celluloid erosion and Kalani shirt staining properties for the nine obtained compounds and six conventionally used compounds.

(1) セルロイドの侵食性試験 眼鏡用セルロイド片に試料を1滴塗り、30℃の恒温室
中に24時間放置した後、水洗、乾燥して外観の変化を
観察した。
(1) Erosion test of celluloid One drop of the sample was applied to a piece of celluloid for eyeglasses, left in a constant temperature room at 30° C. for 24 hours, washed with water, dried, and observed for changes in appearance.

(2)カラーシャツの汚染試験 カラーシャツ用生地(ポリエステル65%、綿35%、
色:ブルー)に試料を1滴塗り、赤外線ランプで30分
乾燥した後、高温用セツクン2gと炭酸ソーダ1gとを
1lの水にとがした溶液を用いて、60℃で30分間洗
浄した。
(2) Contamination test for colored shirts Fabric for colored shirts (65% polyester, 35% cotton,
One drop of the sample was applied to the surface (color: blue), dried with an infrared lamp for 30 minutes, and then washed at 60°C for 30 minutes using a solution of 2 g of high-temperature soap and 1 g of soda carbonate in 1 liter of water.

乾燥後シミの有無をチェックした。After drying, the presence or absence of stains was checked.

表1から明らかなように、本発明に使用する化合物は、
セルロイドの侵食性とカラーシャツの汚染性の問題をと
もに満足させることがわかる。
As is clear from Table 1, the compounds used in the present invention are:
It can be seen that both the corrosive properties of celluloid and the contaminating properties of colored shirts are satisfied.

つぎに本発明を実施例により説明する。Next, the present invention will be explained by examples.

実施例 1 試料No6を用いて、つぎの処方の透明液体整髪料を調
製した。
Example 1 A transparent liquid hair styling product having the following formulation was prepared using sample No. 6.

試料46 22重量%エタノ
ール 42〃ダリセリン
2〃 イオン交換水 34〃香料および
色素 適 量試料腐6に、エタノー
ル、グリセリン、香料および色素を加えて均一になるま
で攪拌し、つぎにイオン交換水を加えて透明液体整髪料
を得た。
Sample 46 22% by weight ethanol 42 Dalycerin
2. Ion-exchanged water 34. Perfumes and pigments Appropriate amounts Ethanol, glycerin, perfumes and pigments were added to Sample 6 and stirred until uniform, and then ion-exchanged water was added to obtain a transparent liquid hair styling product.

この整髪料を眼鏡用セルロイドに塗布し、30℃の恒温
室中に24時間放置したが侵食は見られなかった。
This hair styling product was applied to celluloid for glasses and left in a constant temperature room at 30° C. for 24 hours, but no erosion was observed.

また前述のカラーシャツ用生地に塗布して48時間自然
乾燥させた後洗たくしたが、新しい生地と変化はなく、
汚染は見られなかった。
I also applied it to the colored shirt fabric mentioned above and let it air dry for 48 hours before washing it, but there was no change from the new fabric.
No contamination was observed.

実施例 2 試料No4を用い、つぎの処方で透明ゲル状整髪料を調
製した。
Example 2 A transparent gel hair styling product was prepared using sample No. 4 according to the following formulation.

試料No4 72重量%グ
リセリンモノステアレート 4 〃ソルビッ
ト 4 〃イオン交換水
20 〃香料、色素および防腐
剤 適 量試料A4を60〜65℃に加熱
し、グリセリンモノステアレート、香料、色素および防
腐剤を加え、均一透明溶液になるまで攪拌した後、ソル
ビットを溶解したイオン交換水を攪拌し続けながら加え
た。
Sample No. 4 72% by weight glycerin monostearate 4 Sorbitol 4 Ion exchange water
20 Flavors, pigments and preservatives Appropriate amount Sample A4 was heated to 60-65°C, glycerin monostearate, perfume, pigments and preservatives were added, stirred until a homogeneous and transparent solution was obtained, and the ions in which sorbitol was dissolved were added. Replacement water was added with continued stirring.

溶液が透明になってから急速に冷却して透明ゲル状整髪
料を得た。
After the solution became transparent, it was rapidly cooled to obtain a transparent gel hair styling product.

このゲルは非常に安定で、0〜45℃の範囲で変化はな
かった。
This gel was very stable and did not change in the range of 0-45°C.

セルロイドの侵食およびカラーシャツの汚染について実
施例1と同様に試験を行ったが、まったく問題はなかっ
た。
Tests for celluloid erosion and collar shirt staining were conducted in the same manner as in Example 1, but no problems were found.

実施例 3 試料No6の化合物を用い、つぎの処方でヘヤークリー
ムを調製した。
Example 3 A hair cream was prepared using the compound of sample No. 6 according to the following formulation.

試料No6 28重量%流動パ
ラフィン 10 〃ステアリン酸
1 〃脱水ラノリン
1 〃イオン交換水
60 〃香料および防腐剤
適 量試料No6を60〜65℃に加熱し、流動パ
ラフィン、ステアリン酸、脱水ラノリン、香料および防
腐剤を加えて攪拌し、均一になってから徐々にイオン交
換水を加えてヘヤークリームを得た。
Sample No. 6 28% by weight liquid paraffin 10 Stearic acid
1〃Dehydrated lanolin
1 〃Ion exchange water
60 Flavoring agents and preservatives
An appropriate amount of sample No. 6 was heated to 60-65°C, liquid paraffin, stearic acid, dehydrated lanolin, fragrance and preservative were added and stirred, and after the mixture became homogeneous, ion-exchanged water was gradually added to obtain a hair cream. .

このヘヤークリームはO〜50℃の範囲で安定であり、
外観の変化は認められなかった。
This hair cream is stable in the range of 0 to 50℃,
No change in appearance was observed.

またセルロイドの侵食とカラーシャツの汚染は見られず
、ヘヤートニックをつけた直後に使用しても違和感はな
かった。
In addition, no erosion of the celluloid or contamination of the colored shirt was observed, and there was no discomfort even when used immediately after applying hair tonic.

Claims (1)

【特許請求の範囲】 1 一般式 AO(RO)a(C2H40)bH (ただし、Aは炭素数1〜22の脂肪族炭化水素基、R
は炭素数3〜18のアルキレン基、aはROで示される
アルキレンオキシドの重合数で全体の平均分子量力−5
00〜5000になる整数、bはエチレンオキシドの重
合数で全体の平均分子量の3〜20重量%に相当する整
数。 )で示される化合物の1種または2種以上の混合物を含
有する整髪料。
[Claims] 1 General formula AO(RO)a(C2H40)bH (wherein A is an aliphatic hydrocarbon group having 1 to 22 carbon atoms, R
is an alkylene group having 3 to 18 carbon atoms, a is the polymerization number of alkylene oxide represented by RO, and the overall average molecular weight is -5
b is an integer from 00 to 5,000, and b is an integer corresponding to the polymerization number of ethylene oxide, which corresponds to 3 to 20% by weight of the overall average molecular weight. ) A hair styling product containing one or a mixture of two or more compounds.
JP15184475A 1975-12-22 1975-12-22 Seihatsuriyo Expired JPS584003B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP15184475A JPS584003B2 (en) 1975-12-22 1975-12-22 Seihatsuriyo

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP15184475A JPS584003B2 (en) 1975-12-22 1975-12-22 Seihatsuriyo

Publications (2)

Publication Number Publication Date
JPS5276443A JPS5276443A (en) 1977-06-27
JPS584003B2 true JPS584003B2 (en) 1983-01-24

Family

ID=15527507

Family Applications (1)

Application Number Title Priority Date Filing Date
JP15184475A Expired JPS584003B2 (en) 1975-12-22 1975-12-22 Seihatsuriyo

Country Status (1)

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JP (1) JPS584003B2 (en)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS57165311A (en) * 1981-04-07 1982-10-12 Kao Corp Hair setting agent
JPH0672089B2 (en) * 1984-07-31 1994-09-14 ポーラ化成工業株式会社 Gel hairdressing
JPS6137709A (en) * 1984-07-31 1986-02-22 Pola Chem Ind Inc Transparent gelatinous cosmetic

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JPS5276443A (en) 1977-06-27

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