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JPH035440B2 - - Google Patents

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Publication number
JPH035440B2
JPH035440B2 JP19370382A JP19370382A JPH035440B2 JP H035440 B2 JPH035440 B2 JP H035440B2 JP 19370382 A JP19370382 A JP 19370382A JP 19370382 A JP19370382 A JP 19370382A JP H035440 B2 JPH035440 B2 JP H035440B2
Authority
JP
Japan
Prior art keywords
acylglutamate
alanine
skin
amphoteric surfactant
cleaning
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
JP19370382A
Other languages
Japanese (ja)
Other versions
JPS5984995A (en
Inventor
Hiroshi Nakano
Masahiro Takehara
Noritsugu Ishikawa
Makoto Takai
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.)
Ajinomoto Co Inc
Myoshi Oil and Fat Co Ltd
Original Assignee
Ajinomoto Co Inc
Myoshi Oil and Fat 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 Ajinomoto Co Inc, Myoshi Oil and Fat Co Ltd filed Critical Ajinomoto Co Inc
Priority to JP19370382A priority Critical patent/JPS5984995A/en
Publication of JPS5984995A publication Critical patent/JPS5984995A/en
Publication of JPH035440B2 publication Critical patent/JPH035440B2/ja
Granted legal-status Critical Current

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  • Detergent Compositions (AREA)

Description

【発明の詳細な説明】[Detailed description of the invention]

本発明はN−アシルグルタミン酸塩とβ−アラ
ニン型両性界面活性剤を配合してなる洗浄剤組成
物に関し、その目的とするところは安全性が高
く、皮フおよび毛髪に対し温和であり、しかもす
ぐれた起泡性、洗浄性を有する洗浄剤組成物を提
供することにある。 近年各種洗浄剤に対する安全性への要求がます
ます強くなつてきており、処方を組立てる際の洗
浄剤の活性成分の選定に安全性の高いものが求め
られている。これらの中で天然原料である脂肪酸
およびアミノ酸を用いて得られる界面活性剤が近
年とみに注目され需要が伸びている。その代表的
なものとして、N−アシルグルタミン酸塩が挙げ
られ、すでに固形洗浄剤、液状洗浄剤などの基材
として用いられており(特公昭48−11805号公報、
同49−34725号公報等)、又これを鉱油系、アルコ
ール系洗浄剤に添加してなる皮フを荒らさない洗
浄剤組成物についても提供されている(特公昭39
−29444号公報)。 最近β−アラニン型の両性界面活性剤が注目さ
れており(特開昭51−68609号公報、同54−78704
号公報)、洗浄剤としてすぐれた界面活性能を示
し、乳化、分散、可溶化力に富み、金属石けん
(スカム)の分散力にすぐれ、かつ皮フ、頭髪に
対し低刺激性でマイルドであり、生分解性にすぐ
れていることが認められている。 以上のアミノ酸系界面活性剤は、上記の如く、
合成洗剤に添加したとき優れた皮フ保護効果を有
するが、夫々単品で用いた時、油汚垢の多い汚
物、例えば油の付着した食器の洗浄、ポマードの
付着した毛髪に対しては、乳化力、洗浄力がやや
不足することが指摘されている。そこで本発明者
等はN−アシルグルタミン酸塩とβ−アラニン型
両性界面活性剤との混合物から成る洗浄剤組成物
について種々検討した結果、N−アシルグルタミ
ン酸塩と一般式(A) (但し、式中Rは炭素数6〜18の炭化水素基、
m,nは整数でm=0〜19、n=1〜20、m+n
=1〜20、またMは水素またはNa,Kなどのア
ルカリ金属、アンモニウムあるいは有機アミンを
示す。) で示される両性界面活性剤とを併用したときは、
夫々単独で使用した場合に比して、油汚垢の存在
下でも良好な洗浄力および起泡力を有する製品が
得られること、皮フ保護性が増大し、乳化性、帯
電防止性が付与され、洗浄後の櫛通しが更に向上
することを見出し、本発明を完成するに至つた。 本発明における洗浄剤の形態は用いられる原料
により固形、練、液体と種々の形態のものが得ら
れるが、その形態にかかわらず上に述べた特徴を
如何なく発揮することが判明した。 ここで用いられるN−アシルグルタミン酸塩の
アシル基としては炭素数8〜22の脂肪酸残基、例
えば2−エチルヘキサノイル、ラウロイル、パル
ミトイル、ステアロイル、オレオイル等の単一脂
肪酸のアシルの他、硬化牛脂脂肪酸アシル、ヤシ
油脂肪酸アシル等の混合脂肪酸アシルが用いら
れ、塩としては、リチウム、ナトリウム、カリウ
ム、アンモニウム、アルキロールアミノ、塩基性
アミノ酸などのモノ、ジ当量塩が洗浄剤の形態に
より適宜選択される。 尚一方の成分であるβ−アラニン型両性界面活
性剤一般式(A)においてRは炭素数6〜18の炭化水
素基であつて、例えばオクチル、デシル、ラウリ
ル、ミリスチル、パルミチル、ステアリル、イソ
ステアリル等の単独アルキルあるいはこれらの混
合したものが挙げられ、mは0〜19の整数、nは
1〜20の整数であり、かつm+nは1〜20の整
数、またMは水素またはNa,Kなどのアルカリ
金属、またはアンモニウム、あるいはモノエタノ
ールアミン、ジエタノールアミン、トリエタノー
ルアミン、リジン等の有機アミンが挙げられる。 N−アシルグルタミン酸塩と前記一般式(A)で示
されるβ−アラニン型両性界面活性剤との配合比
は、通常重量比にして9:1〜1:9が用いられ
るが、特に8:2〜4:6付近で洗浄力、起泡力
に於て優れた相乗効果がみられる。 本発明の洗浄剤組成物にはその他の界面活性
剤、例えば、他のN−アシルアミノ酸塩、N−ア
シルプロテイン、アルキルサルフエート、アルキ
ルスルホアセテート、アルキルエーテルサルフエ
ートなどの陰イオン界面活性剤、アルキロールア
ミドなどの非イオン界面活性剤、イミダゾリン系
などの両性界面活性剤が必要に応じて用いられ、
またアルキルアンモニウム塩などの陽イオン界面
活性剤を配合することも可能であり、更にはクエ
ン酸、アミノ酸、プロテイン酸、硫酸ナトリウム
のごとき有機又は無機ビルダー、可溶化剤、稀釈
剤、香料、色素などを適宜配合することができ
る。 以下、実施例により更に詳しく説明する。尚、
実施例に於ける百分率は全て重量に基づくもので
ある。 実施例1 液体洗剤
The present invention relates to a cleansing composition containing an N-acylglutamate and a β-alanine type amphoteric surfactant, which aims to be highly safe, gentle on skin and hair, and moreover, An object of the present invention is to provide a cleaning composition having excellent foaming properties and cleaning properties. In recent years, demands on the safety of various cleaning agents have become stronger and stronger, and there is a need for highly safe active ingredients in cleaning agents when formulating formulations. Among these, surfactants obtained using fatty acids and amino acids, which are natural raw materials, have recently attracted attention and demand is increasing. A typical example is N-acylglutamate, which has already been used as a base material for solid detergents, liquid detergents, etc. (Japanese Patent Publication No. 48-11805,
Publication No. 49-34725, etc.), and detergent compositions that do not irritate the skin, which are obtained by adding this to mineral oil-based or alcohol-based detergents, have also been proposed (Japanese Patent Publication No.
-29444). Recently, β-alanine type amphoteric surfactants have attracted attention (Japanese Patent Application Laid-open Nos. 51-68609 and 54-78704).
As a detergent, it exhibits excellent surfactant ability, has excellent emulsifying, dispersing, and solubilizing power, and has excellent dispersing power for metal soap (scum), and is mild and non-irritating to the skin and hair. It has been recognized that it has excellent biodegradability. The above amino acid surfactants are as described above,
When added to synthetic detergents, it has an excellent skin protection effect, but when used alone, it has no emulsifying power for cleaning dirt with a lot of oil stains, such as cleaning dishes with oil on it, and hair with pomade on it. It has been pointed out that the cleaning power is somewhat insufficient. Therefore, the present inventors conducted various studies on detergent compositions comprising a mixture of N-acylglutamate and a β-alanine type amphoteric surfactant, and found that N-acylglutamate and the general formula (A) (However, in the formula, R is a hydrocarbon group having 6 to 18 carbon atoms,
m and n are integers, m=0 to 19, n=1 to 20, m+n
=1 to 20, and M represents hydrogen, an alkali metal such as Na or K, ammonium, or an organic amine. ) When used in combination with an amphoteric surfactant shown in
Compared to when each is used alone, a product can be obtained that has good detergency and foaming power even in the presence of oil stains, has increased skin protection, and has emulsifying and antistatic properties. They discovered that the combing ability after washing was further improved and completed the present invention. The cleaning agent of the present invention can take various forms, such as solid, kneaded, and liquid, depending on the raw materials used, but it has been found that the above-mentioned characteristics are fully exhibited regardless of the form. The acyl group of the N-acylglutamate used here includes fatty acid residues having 8 to 22 carbon atoms, such as acyl of a single fatty acid such as 2-ethylhexanoyl, lauroyl, palmitoyl, stearoyl, and oleoyl, as well as hardened Mixed fatty acid acyls such as beef tallow fatty acid acyl and coconut oil fatty acid acyl are used, and as salts, mono- and di-equivalent salts such as lithium, sodium, potassium, ammonium, alkylolamino, and basic amino acids are used as appropriate depending on the form of the cleaning agent. selected. In the general formula (A) of β-alanine type amphoteric surfactant which is one component, R is a hydrocarbon group having 6 to 18 carbon atoms, such as octyl, decyl, lauryl, myristyl, palmityl, stearyl, isostearyl. Examples include individual alkyl such as or a mixture thereof, where m is an integer of 0 to 19, n is an integer of 1 to 20, and m+n is an integer of 1 to 20, and M is hydrogen or Na, K, etc. Examples include alkali metals, ammonium, and organic amines such as monoethanolamine, diethanolamine, triethanolamine, and lysine. The blending ratio of N-acylglutamate and the β-alanine type amphoteric surfactant represented by the general formula (A) is usually 9:1 to 1:9 by weight, but especially 8:2. An excellent synergistic effect in detergency and foaming power is seen at around 4:6. The cleaning composition of the present invention may include other surfactants, such as anionic surfactants such as other N-acyl amino acid salts, N-acyl proteins, alkyl sulfates, alkyl sulfoacetates, alkyl ether sulfates, Nonionic surfactants such as alkylolamides and amphoteric surfactants such as imidazolines are used as necessary.
It is also possible to incorporate cationic surfactants such as alkylammonium salts, as well as organic or inorganic builders such as citric acid, amino acids, protein acids, sodium sulfate, solubilizers, diluents, fragrances, pigments, etc. can be appropriately blended. A more detailed explanation will be given below using examples. still,
All percentages in the examples are by weight. Example 1 Liquid detergent

〔洗浄力測定法〕[Cleaning power measurement method]

VS改良法(油化学24(9),595,(1975))に準じ
て行なつた。但し試料濃度1.5g/で測定した。 〔洗浄力測定結果〕 第1表より明らかな如く、両アミノ酸系界面活
性剤の間に比較的広い配合割合において洗浄力に
相乗効果、すなわち皿洗い枚数の増加が認められ
た。
It was carried out according to the improved VS method (Oil Chemistry 24 (9), 595, (1975)). However, the measurement was performed at a sample concentration of 1.5 g/. [Results of Detergent Power Measurement] As is clear from Table 1, a synergistic effect on the detergent power, that is, an increase in the number of dishes washed, was observed in a relatively wide range of blending ratios between the two amino acid surfactants.

【表】 実施例2 液体シヤンプー (%) N−ココイルグルタミン酸モノトリエタノール
アシ塩 15 β−アラニン型両性界面活性剤(A) 5 ヤシ油脂肪酸ジエタノールアミド 2 ピログルタミン酸ナトリウム(50%水溶液) 2 水 76 計100 上記の配合組成物により、皮フおよび頭髪に温
和で、起泡力および泡の保持性に優れ、又使用後
の感触もすぐれた液体シヤンプーが得られた。 尚、上記組成中、β−アラニン型両性界面活性
剤(A)の添加の有無による泡立ちの良さをロスマイ
ルス法により測定した結果、第2表から明らかな
如く、β−アラニン型両性界面活性剤を添加する
ことにより泡立ちが良好となることが認められ
た。
[Table] Example 2 Liquid shampoo (%) N-cocoylglutamic acid monotriethanolic acid salt 15 β-alanine type amphoteric surfactant (A) 5 Coconut oil fatty acid diethanolamide 2 Sodium pyroglutamate (50% aqueous solution) 2 Water 76 Total: 100 With the above-mentioned blended composition, a liquid shampoo was obtained that was gentle on the skin and hair, had excellent foaming power and foam retention, and also had an excellent feel after use. In addition, as a result of measuring the foaming quality according to the presence or absence of the β-alanine type amphoteric surfactant (A) in the above composition by the Ross Miles method, as is clear from Table 2, the β-alanine type amphoteric surfactant (A) It was found that foaming was improved by adding .

【表】 実施例3 固型洗剤 N−アシルグルタミン酸モノナトリウム*63% N−(2−ヒドロキシアルキル)−N−(2−ヒ
ドロキシエチル)−β−アラニン** 21% セチルアルコール 10% 水 6% 計100% (* アシル基の組成は半硬化牛脂脂肪酸とヤ
シ油脂肪酸の8:2組成物 ) (** 2−ヒドロキシアルキル基はC12
C14) 上記配合物の場合、N−アシルグルタミン酸モ
ノナトリウムを除く3種の配合物を混合し、加温
乳化させた後、N−アシルグルタミン酸モノナト
リウムに加え、小型ロールで充分に混練する。こ
れを口金を40〜50℃に保持した小型石けん試作装
置を用いて押し出し、得られた棒状洗剤を足踏式
型打機で成型し、固型洗剤を得た。本品は皮フに
温和で、豊かな泡立ち保持性を有し、また、硬水
中での使用においても、金属石けん(スカム)の
生成がなく泡立ちも良好であつた。 実施例4 洗顔用練状洗剤 N−ミリストイルグルタミン酸モノカリウム
25% N−(2−ヒドロキシドデシル)−N−(2−ヒ
ドロキシエチル)−β−アラニン 10% N−(2−ヒドロキシアルキル)−N−(ポリオ
キシエチレン(3モル)−β−アラニン 2% プロピレングリコール 10% ポリエチレングリコール1500 5% 水 48% 計100% 上記配合組成物により、皮フに温和で、起泡性
の優れた洗顔用練状洗剤が得られた。 実施例5 洗顔用透明練状洗剤 N−ココイルグルタミン酸モノナトリウム25% N−(2−ヒドロキシドデシル)−N−(ポリオ
キシエチレン(3モル)−β−アラニン 25% プロピレングリコール 5% 水 45% 上記の配合組成物を80℃に保つた真空乳化機内
にて撹拌しつつ均一に溶解せしめる。その後、室
温まで冷却すると皮膚に温和かつ使用後にしつと
りとした感触を与え、しかも美麗な透明ゲル状の
外観を呈する洗顔料が得られた。
[Table] Example 3 Solid detergent Monosodium N-acylglutamate *63% N-(2-hydroxyalkyl)-N-(2-hydroxyethyl)-β-alanine** 21% Cetyl alcohol 10% Water 6% Total 100% (* Composition of acyl group is 8:2 composition of semi-hardened beef tallow fatty acid and coconut oil fatty acid) (** 2-hydroxyalkyl group is C 12 ~
C 14 ) In the case of the above formulation, three types of formulations except monosodium N-acylglutamate are mixed, emulsified by heating, and then added to monosodium N-acylglutamate and thoroughly kneaded using a small roll. This was extruded using a small soap prototype device whose mouthpiece was kept at 40 to 50°C, and the resulting bar-shaped detergent was molded using a foot-type molding machine to obtain a solid detergent. This product was gentle on the skin and had a rich foaming and retaining property, and even when used in hard water, no metal soap (scum) was formed and the foaming was good. Example 4 Facial cleansing paste monopotassium N-myristoylglutamate
25% N-(2-hydroxydodecyl)-N-(2-hydroxyethyl)-β-alanine 10% N-(2-hydroxyalkyl)-N-(polyoxyethylene (3 moles)-β-alanine 2% Propylene glycol 10% Polyethylene glycol 1500 5% Water 48% Total 100% A facial cleansing paste that was gentle on the skin and had excellent foaming properties was obtained. Example 5 Transparent facial cleansing paste Detergent monosodium N-cocoylglutamate 25% N-(2-hydroxydodecyl)-N-(polyoxyethylene (3 mol)-β-alanine 25% propylene glycol 5% water 45% The above blended composition was heated at 80°C Dissolve it uniformly while stirring in a vacuum emulsifier kept at room temperature.Then, when it is cooled to room temperature, it produces a facial cleanser that is gentle on the skin and leaves the skin feeling moisturized after use, as well as having a beautiful transparent gel-like appearance. Obtained.

Claims (1)

【特許請求の範囲】 1 N−アシルグルタミン酸塩と下記一般式(A)で
示されるβ−アラニン型両性界面活性剤を含有す
ることを特徴とする洗浄組成物。 (但し式中Rは炭素数6〜18の炭化水素基、
m,nは整数でm=0〜19、n=1〜20、m+n
=1〜20、またMは水素、アルカリ金属、アンモ
ニウムあるいは有機アミンを示す。)
[Scope of Claims] A cleaning composition characterized by containing 1 N-acylglutamate and a β-alanine type amphoteric surfactant represented by the following general formula (A). (However, in the formula, R is a hydrocarbon group having 6 to 18 carbon atoms,
m and n are integers, m=0 to 19, n=1 to 20, m+n
=1 to 20, and M represents hydrogen, alkali metal, ammonium or organic amine. )
JP19370382A 1982-11-04 1982-11-04 Detergent composition Granted JPS5984995A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP19370382A JPS5984995A (en) 1982-11-04 1982-11-04 Detergent composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP19370382A JPS5984995A (en) 1982-11-04 1982-11-04 Detergent composition

Publications (2)

Publication Number Publication Date
JPS5984995A JPS5984995A (en) 1984-05-16
JPH035440B2 true JPH035440B2 (en) 1991-01-25

Family

ID=16312373

Family Applications (1)

Application Number Title Priority Date Filing Date
JP19370382A Granted JPS5984995A (en) 1982-11-04 1982-11-04 Detergent composition

Country Status (1)

Country Link
JP (1) JPS5984995A (en)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2511776B2 (en) * 1992-10-02 1996-07-03 三洋化成工業株式会社 Detergent composition
JPH06248290A (en) * 1993-02-26 1994-09-06 Miyoshi Oil & Fat Co Ltd Cleaning agent composition
JP2001220596A (en) * 2000-02-09 2001-08-14 Miyoshi Oil & Fat Co Ltd Ampholytic surfactant
MY186674A (en) * 2018-06-07 2021-08-05 Kl Kepong Oleomas Sdn Bhd A syndet bar composition

Also Published As

Publication number Publication date
JPS5984995A (en) 1984-05-16

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