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JPH0433839B2 - - Google Patents
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JPH0433839B2 - - Google Patents

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Publication number
JPH0433839B2
JPH0433839B2 JP10531483A JP10531483A JPH0433839B2 JP H0433839 B2 JPH0433839 B2 JP H0433839B2 JP 10531483 A JP10531483 A JP 10531483A JP 10531483 A JP10531483 A JP 10531483A JP H0433839 B2 JPH0433839 B2 JP H0433839B2
Authority
JP
Japan
Prior art keywords
acid
transparent gel
alkali metal
amino acid
salt
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
JP10531483A
Other languages
Japanese (ja)
Other versions
JPS59230099A (en
Inventor
Koichiro Sagawa
Hiroshi Yokota
Masahiro Takehara
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
Original Assignee
Ajinomoto Co Inc
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 filed Critical Ajinomoto Co Inc
Priority to JP10531483A priority Critical patent/JPS59230099A/en
Publication of JPS59230099A publication Critical patent/JPS59230099A/en
Publication of JPH0433839B2 publication Critical patent/JPH0433839B2/ja
Granted legal-status Critical Current

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Description

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

本発明は起泡性,洗浄性に優れ,皮フ及び眼粘
膜に対する作用が温和でしかも良好な保存安全性
を有する透明ゲル状洗浄剤組成物に関する。 従来、透明洗浄剤としては脂肪酸のアルカリ金
属塩にシヨ糖等の炭水化物を加え、エタノール及
びグリセリン等で透明化した固型透明石ケンが用
いられている。しかし、かかる透明石ケンは起泡
性が悪いこと、使用中に吸水膨澗し、溶崩、失透
が起り易く、また、pHが高く、皮フを荒らす等
の障害を与え易い、製造面に於ても型枠成型後エ
タノールを徐々に揮散させて行われているため、
製造に長時間を要する等々の欠点を有する。 上述した如き多くの欠点を有するにも拘らず透
明石ケンが通常の洗浄剤に較べ高い商品価値を有
しているのは、その透明性に由来する美しさ故で
ある。 近年、この透明石ケンの持つ美しさ、高級感を
保持しつつ上述の欠点を解消する目的で、皮フ及
び眼粘膜に対する作用が温和でしかも使用感に優
れるアミノ酸系界面活性剤を用いた透明ゲル状洗
浄剤の開発が種々検討されている。例えば、N‐
アシル酸性アミノ酸トリエタノールーアミン塩を
用いた例(特開昭50−75576号公報)、或いは中和
当量1.5以上のN‐アシル酸性アミノ酸塩を用い
た例(特開昭56−76500号公報)等がそれである。
しかしながら、N‐アシル酸性アミノ酸塩は皮フ
や眼粘膜に対する作用が温和であるという特長を
有する反面、油汚垢存在下に於ける起泡力が若干
不足し、特にその傾向はトリエタノームアミン塩
及び中和当量1.5以上の塩を用いた場合に顕著で
ある。また、N‐アミル酸性アミノ酸塩の1種で
あるN‐アシルグルタミン酸塩にポリエチレング
リコール、脂肪酸ジエタノールアミド、アシル化
コラーゲンペプタイドアルカリ金属塩等を配合し
てなる透明ゲル状洗浄剤を得る試みもなされてい
るが(特開昭55−69699号公報)、本発明者が検討
したところによれば、その粘度は低く透明ゲルと
はなり得ず、しかもアシル化コラーゲンペプタイ
ドアルカリ金属塩由来の異臭が残る為、実用には
供し難いことが認められた。 一方、皮フ及び眼粘膜に対する作用が温和な界
面活性剤としては更にイミダゾリン系両性界面活
性剤が挙げられるが、このものはN‐アシル酸性
アミノ酸塩と同様、それ単独では油汚垢の存在下
に於ては起泡力、洗浄力が必ずしも十分ではな
い。 本発明者らは、N‐アシル酸性アミノ酸塩或い
はイミダゾリン系両性界面活性剤を主成分とする
透明ゲル状洗浄剤の泡性能を改良せんとして、脂
肪酸ジエタノールアミド、アルキルアミンオキサ
イド等の増泡剤や強力な洗浄力を有するアルキル
サルフエート等の合成系界面活性剤の配合を試み
たところ、これらの界面活性剤はこれを小量配合
した場合ではその効果が充分ではなく、また多量
に配合すると透明性及び安全性が失なわれて了う
ことを確認した。 本発明者はかかる実状に鑑み、高い安全性、皮
フ眼粘膜に対する温和な作用という好ましい特長
を保持し、しかも起泡力、洗浄力の改善された透
明ゲル状洗浄剤を開発すべく更に検討を続けたと
ころ、N‐アシル酸性アミノ酸塩とイミダゾリン
系両性界面活性剤とを後述の如き特定割合にて配
合した場合には、特にゲル化剤或いは増粘剤等の
添加物を加えずとも良好な保存安定性を示し、優
れた起泡力、洗浄力を有する透明ゲル状洗浄剤が
得られることを見い出し、本発明を完成するに至
つた。 即ち、本発明は(A)下記一般式()で表わされ
るアミノ酸系界面活性剤と(B)下記一般式()で
表わされるイミダゾリン系両性界面活性剤と(C)水
を必須成分とする洗剤組成物に於て、(A)成分に対
する(B)成分の配合割合が重量比で8/2〜1/9
でありかつ界面活性剤濃度を40〜70の重量%の範
囲に調整してある透明ゲル状洗浄剤組成物であ
る。 (但し、R1は炭素数7〜21のアルキル基または
アルケニル基、M1,M2はそれぞれ水素原子また
はアルカリ金属、nは1または2つ整数を示す。) (但し、R2は炭素数7〜21のアルキル基または
アルケニル基、R3は水素原子、アルカリ金属ま
たは CH2COOM3、ZはCOOM3,CH2COOM3または
The present invention relates to a transparent gel-like cleansing composition that has excellent foaming properties and cleansing properties, has mild effects on the skin and eye mucous membranes, and has good storage safety. Conventionally, solid transparent soaps made by adding carbohydrates such as sucrose to alkali metal salts of fatty acids and making them transparent with ethanol, glycerin, etc. have been used as transparent cleaning agents. However, such transparent soaps have poor foaming properties, tend to swell upon water absorption, dissolve, and devitrify during use, and have a high pH, which can easily cause problems such as roughening the skin. Even in this process, the ethanol is gradually volatilized after forming the mold, so
It has drawbacks such as requiring a long time to manufacture. Despite having many of the drawbacks mentioned above, transparent soap has a higher commercial value than ordinary detergents because of its beauty derived from its transparency. In recent years, in order to eliminate the above-mentioned drawbacks while retaining the beauty and luxury of transparent soap, transparent soap has been developed using an amino acid-based surfactant that has a mild effect on the skin and eye mucous membranes and is easy to use. Various efforts are being made to develop gel-like cleaning agents. For example, N-
An example using an acyl acidic amino acid triethanol-amine salt (JP-A-50-75576) or an example using an N-acyl acidic amino acid salt with a neutralization equivalent of 1.5 or more (JP-A-56-76500) etc. is that.
However, while N-acyl acidic amino acid salts have a mild effect on the skin and eye mucous membranes, they are slightly lacking in foaming power in the presence of oil stains, and this tendency is particularly evident with triethanamine salts. This is noticeable when a salt with a neutralization equivalent of 1.5 or more is used. In addition, attempts have also been made to obtain a transparent gel-like detergent made by blending polyethylene glycol, fatty acid diethanolamide, acylated collagen peptide alkali metal salt, etc. with N-acylglutamate, which is a type of N-amyl acidic amino acid salt. However, according to the present inventor's study, the viscosity is low and it cannot form a transparent gel, and furthermore, the odor derived from the alkali metal salt of acylated collagen peptide remains. It was recognized that it is difficult to put it into practical use. On the other hand, imidazoline-based amphoteric surfactants are examples of surfactants that have mild effects on the skin and ocular mucosa, but like N-acyl acidic amino acid salts, these surfactants alone do not react well in the presence of oil stains. In some cases, the foaming power and cleaning power are not necessarily sufficient. The present inventors aimed to improve the foaming performance of transparent gel-like detergents containing N-acyl acidic amino acid salts or imidazoline amphoteric surfactants as main components, using foaming agents such as fatty acid diethanolamide and alkylamine oxides, When we tried to incorporate synthetic surfactants such as alkyl sulfates, which have strong cleaning power, we found that these surfactants were not effective enough when used in small amounts, and that they became transparent when added in large amounts. It was confirmed that safety and safety were lost. In view of these circumstances, the present inventors conducted further studies in order to develop a transparent gel-like cleansing agent that maintains the favorable features of high safety and mild action on the skin and eye mucous membranes, and has improved foaming power and cleansing power. As a result, when the N-acyl acidic amino acid salt and the imidazoline amphoteric surfactant were blended in a specific ratio as described below, the results were good even without the addition of additives such as gelling agents or thickeners. The present inventors have discovered that a transparent gel-like detergent can be obtained that exhibits excellent storage stability, excellent foaming power, and detergent power, and has completed the present invention. That is, the present invention provides a detergent containing (A) an amino acid surfactant represented by the following general formula (), (B) an imidazoline amphoteric surfactant represented by the following general formula (), and (C) water as an essential component. In the composition, the weight ratio of component (B) to component (A) is 8/2 to 1/9.
This is a transparent gel-like cleaning composition in which the surfactant concentration is adjusted to a range of 40 to 70% by weight. (However, R 1 is an alkyl group or alkenyl group having 7 to 21 carbon atoms, M 1 and M 2 are each a hydrogen atom or an alkali metal, and n is an integer of 1 or 2.) (However, R 2 is an alkyl group or alkenyl group having 7 to 21 carbon atoms, R 3 is a hydrogen atom, an alkali metal or CH 2 COOM 3 , and Z is COOM 3 , CH 2 COOM 3 or

【式】M3は水素原子、アルカリ 金属またはアルカノールアミンを示す。) 本発明によれば、アミノ酸系界面活性剤及びイ
ミダゾリン系両性界面活性剤の有する好ましい特
性、つまり皮フ及び眼粘膜に対する温和な作用を
具備し、しかも起泡、洗浄性に優れ、保存安定性
良好な透明ゲル状洗浄剤を容易に製造することが
できる。 本発明に於て一般式()表示のアミノ酸系界
面活性剤としては、例えばN‐ラウロイルアスパ
ラギン酸、N‐ミリストイルアスパラギン酸、
N‐パルミトイルアスパラギン酸、N‐ステアロ
イルアスパラギン酸、N‐オレオイルアスパラギ
ン酸、N‐イソステアロイルアスパラギン酸等単
一脂肪酸アシルアスパラギン酸、N‐ヤシ油脂肪
酸アシルアスパラギン酸、N‐硬化牛脂脂肪酸ア
シルアスパラギン酸等の混合脂肪酸アシルアスパ
ラギン酸、N‐ラウロイルグルタミン酸、N‐ミ
リストイルグルタミン酸、N‐パルミトイルグル
タミン酸、N−ステアロイルグルタミン酸、N‐
オレオイルグルタミン酸、N‐イソステアロイル
グルタミン酸等の単一脂肪酸アシルグルタミン
酸、N‐ヤシ油脂肪酸アシルグルタミン酸、N‐
硬化牛脂脂肪酸アシルグルタミン酸等の混合脂肪
酸アシルグルタミン酸またはこれらの混合物及び
これらナトリウム、カリウム、リチウム等のアル
カリ金属塩が挙げられる。尚、アミノ酸成分は、
光学活性体またはラセミ体のいずれであつてもよ
い。 また、本発明に於て用いられる尚一方の成分で
ある一般式()表示の両性界面活性剤として
は、例えば以下の化学式で表わされる化合物(
―1)〜(―7)が好ましく挙げられる。 本発明の透明ゲル状洗浄剤組成物に於て、(A)ア
ミノ酸系界面活性剤と(B)イミダゾリン系両性界面
活性剤の配合割合(A)/(B)は重量比で8/2〜1/
9好ましくは6/4〜4/6であり、この配合比
よりアミノ酸系界面活性剤が多い場合は結晶化が
起り易く、得られる透明ゲルの低温安定性が損わ
れ、また少ない場合では起泡力、洗浄力が不足す
る。また、界面活性剤、(A)及び(B)成分の全濃度は
40〜70重量%、好ましくは50〜60重量%であり、
かかる濃度より低濃度では粘度低下が起り、流動
性液体への転移が起り易く、また高濃度では固く
取扱いが不便となるばかりか低温に於ける失透、
固結が起り易い。 本発明の透明ゲル状洗浄剤を製造するには、ア
ミノ酸系界面活性剤とイミダゾリン系両性界面活
性剤と水とを上述の如き割合にて配合し、80〜90
℃で加熱溶解後放冷すればよい。この際溶解を容
易にするためエタノール等の低級アルコールを適
量添加するのがよい。 本発明の透明ゲル状洗浄剤の製造に際して、必
要に応じグリセリン、エチレングリコール、エチ
レングリコール、プロピレングリコール、ソルビ
ツトなどの多価アルコール及び尿素、チオ尿素、
マルチトールなどの透明化剤、香料、着色料、
α‐トコフエロール等の酸化防止剤、クエン酸、
アミノ酸、プロテイン、硫酸ナトリウムの如き有
機または無機ビルダー等を適宜配合することがで
きる。 更に、洗浄性や泡立ちを調整する目的で他のア
ニオン界面活性剤、カチオン界面活性剤、非イオ
ン界面活性剤を本発明の目的を阻害しない範囲内
で添加することは何等差支えない。これらのもの
には、例えば脂肪酸石ケン、高級アルコール硫酸
エステル塩、ポリオキシエチレン高級アルコール
リン酸エステル及びその塩、ポリオキシエチレン
高級脂肪酸リン酸エステル及びその塩、スルフオ
ン化高級脂肪酸アルコールエステル塩、高級アル
コールスルホコハク酸エステル塩、イセチオン酸
高級脂肪酸エステル塩、α‐スルホ高級アルコー
ル酢酸エステル塩、ラウリン酸ジエタノールアミ
ド、ステアリン酸モノエタノールアミドなどの高
級脂肪酸とアルキロールアミンの縮合物及びその
エチレンオシサイド付加物、N‐アシル塩基性ア
ミノ酸塩、N‐アシルペプタイドなどが挙げられ
る。 以下、実施例により具体的に説明する。尚、実
施例中に於る%はすべて重量に基づくものであ
る。 実施例 1 洗顔料組成物 N‐ラウロイル‐L‐グルタミン酸モノナトリ
ウム塩 25.0% イミダゾリン系両性界面活性剤(前記‐1
式) 25.0% 香 料 0.3% 水 49.7% 計100.0% 香料を除く上記組成物にエタノールを適量加
え、80〜90℃にて加熱し均一に溶解させる。しか
る後エタノールを回収し、約60℃に冷却した時点
で香料を加え室温で放置すると透明ゲル状の洗顔
料組成物が得られた。 実施例 2 洗顔料組成物 N‐ヤシ油脂肪酸アシル‐L‐グルタミン酸モ
ノナトリウム 40.0% イミダゾリン系両性界面活性剤(前記‐4
式) 10.0% 香 料 0.3% グルセリン 5.0% 水 44.7% 計100.0% 実施例1に準じた方法で上記組成物を混合、溶
解後放冷し、透明ゲル状洗顔料組成物を得た。 実施例 3 洗顔料組成物 N‐ミリストイル‐L−アスパラギン酸ジカリ
ウム塩 5.0% イミダゾリン系両性界面活性剤(前記‐6
式) 40.0% 香 料 0.3% ヤシ油脂肪酸ジエタノールアミド 5.0% 水 49.7% 計100.0% 実施例1に準じた方法で上記化合物を混合、溶
解後放令し、透明ゲル状洗顔料組成物を得た。 実施例 4 洗顔料組成物 N‐硬化牛脂油脂肪酸アシル‐L−グルタミン
酸モノナトリウム塩5.0% イミダゾリン系両性界面活性剤(前記‐7
式) 35.0% N‐ラウロイルザルコシンナトリウム 5.0% 香 料 0.3% グリセリン 5.0% 水 49.7% 計100.0% 実施例1に準じた方法で上記組成物を混合、溶
解後放冷し、透明ゲル状洗顔料組成物を得た。 実施例 5 コンデイシヨニングシヤンプー組成物 N‐ラウロイル‐DL‐グルタミン酸1.5ナトリ
ウム塩 10.0% N‐オレオイル‐DL‐アスパラギン酸モノナ
トリウム塩 10.0% イミダゾリン系両性界面活性剤(前記‐3
式) 40.0% グリセリン 5.0% カチオン化セルロース 1.0% 香 料 0.3% 水 33.7% 計100.0% 実施例1に準じた方法で上記組成物を混合、溶
解後放冷し、透明ゲル状のコンデイシヨニングシ
ヤンプー組成物を得た。 実施例1〜5の洗浄剤組成物の保存安定性、官
能試験、皮フー次刺激性試験を下記の方法に基づ
いて行つた。保存安定性試験 0℃及び40℃の恒温室に2週間放置後の状態を
目視判定した。 ◎:極めて良好の透明ゲル状態 ○:良好な透明ゲル状態 ×:失透、固結、或いは液化官能試験 18〜30才の女性30名をパネラーとし、洗顔料に
関しては手及び顔を、シヤンプーに関しては頭髪
を洗浄してもらい、良いと答えた人数で表示し
た。皮フー次刺激性試験 ニユージーランドホワイト雄ウサギ10匹を用
い、各試料の10%水溶液の24時間クローズドパツ
チテストを行つた。判定は下記のDraize法に従
つた。 Draize法 A紅斑と痂皮形成 紅斑なし 0 非常にわずかな紅斑 1 明確な紅斑 2 中度から重度の紅斑 3 ひどい紅斑(暗赤色)とわずかな痂皮形成
4 B浮腫形成 浮腫なし 0 非常にわずかな浮腫 1 軽度浮腫(明確な膨隆、周囲が明瞭) 2 中度浮腫(膨隆の高さ1mm位) 3 重度浮腫(膨隆の高さ1mm以上) 4 判定 Σ(A+B)÷10 ≦2 Mild 〃 <5 Moderate 〃 ≧5 Severe
[Formula] M 3 represents a hydrogen atom, an alkali metal or an alkanolamine. ) According to the present invention, the present invention has the desirable properties of amino acid-based surfactants and imidazoline-based amphoteric surfactants, that is, mild action on the skin and eye mucous membranes, as well as excellent foaming and cleansing properties, and storage stability. A good transparent gel-like cleaning agent can be easily produced. In the present invention, examples of the amino acid surfactant represented by the general formula () include N-lauroyl aspartic acid, N-myristoyl aspartic acid,
N-palmitoyl aspartic acid, N-stearoyl aspartic acid, N-oleoyl aspartic acid, N-isostearoyl aspartic acid, etc. Single fatty acid acylaspartic acid, N-coconut oil fatty acid acylaspartic acid, N-hydrogenated beef tallow fatty acid acylaspartic acid Mixed fatty acids such as acylaspartic acid, N-lauroylglutamic acid, N-myristoylglutamic acid, N-palmitoylglutamic acid, N-stearoylglutamic acid, N-
Single fatty acid acylglutamic acid such as oleoylglutamic acid, N-isostearoylglutamic acid, N-coconut oil fatty acid acylglutamic acid, N-
Examples include mixed fatty acid acylglutamic acids such as hardened beef tallow fatty acid acylglutamic acid, mixtures thereof, and alkali metal salts thereof such as sodium, potassium, and lithium. In addition, the amino acid components are
It may be either an optically active form or a racemic form. Further, as the amphoteric surfactant represented by the general formula (), which is one of the components used in the present invention, for example, a compound represented by the following chemical formula (
-1) to (-7) are preferred. In the transparent gel-like cleaning composition of the present invention, the blending ratio (A)/(B) of (A) amino acid surfactant and (B) imidazoline amphoteric surfactant is 8/2 to 8/2 by weight. 1/
9 The ratio is preferably 6/4 to 4/6; if the amino acid surfactant is more than this ratio, crystallization tends to occur and the low-temperature stability of the resulting transparent gel is impaired, and if it is less, foaming may occur. Power and cleaning power are insufficient. In addition, the total concentration of surfactant, components (A) and (B) is
40-70% by weight, preferably 50-60% by weight,
If the concentration is lower than this, the viscosity decreases and the transition to a fluid liquid is likely to occur, and if the concentration is higher, it not only becomes hard and inconvenient to handle, but also devitrification occurs at low temperatures.
Caking is likely to occur. In order to produce the transparent gel-like cleaning agent of the present invention, an amino acid surfactant, an imidazoline amphoteric surfactant, and water are blended in the above-mentioned proportions.
The solution may be heated and dissolved at ℃ and then allowed to cool. At this time, it is preferable to add an appropriate amount of lower alcohol such as ethanol to facilitate dissolution. When producing the transparent gel-like cleaning agent of the present invention, polyhydric alcohols such as glycerin, ethylene glycol, propylene glycol, sorbitol, urea, thiourea,
Clarifying agents such as maltitol, fragrances, colorants,
Antioxidants such as α-tocopherol, citric acid,
Amino acids, proteins, organic or inorganic builders such as sodium sulfate, etc. can be blended as appropriate. Furthermore, for the purpose of adjusting detergency and foaming, other anionic surfactants, cationic surfactants, and nonionic surfactants may be added within a range that does not impede the purpose of the present invention. These include, for example, fatty acid soap, higher alcohol sulfate ester salt, polyoxyethylene higher alcohol phosphate ester and its salt, polyoxyethylene higher fatty acid phosphate ester and its salt, sulfonated higher fatty acid alcohol ester salt, higher Condensates of higher fatty acids and alkylolamines such as alcohol sulfosuccinate salts, isethionic acid higher fatty acid ester salts, α-sulfo higher alcohol acetate salts, lauric acid diethanolamide, stearic acid monoethanolamide, and their ethylene oxide adducts , N-acyl basic amino acid salts, N-acyl peptides, and the like. Hereinafter, this will be explained in detail using examples. All percentages in the examples are based on weight. Example 1 Facial cleansing composition N-lauroyl-L-glutamic acid monosodium salt 25.0% Imidazoline amphoteric surfactant (-1
Formula) 25.0% Fragrance 0.3% Water 49.7% Total 100.0% Add an appropriate amount of ethanol to the above composition excluding the fragrance, and heat at 80 to 90°C to uniformly dissolve. Thereafter, the ethanol was collected, and when it was cooled to about 60°C, a fragrance was added and left at room temperature to obtain a transparent gel-like facial cleansing composition. Example 2 Facial cleansing composition Monosodium N-coconut oil fatty acyl-L-glutamate 40.0% Imidazoline amphoteric surfactant (-4)
Formula) 10.0% Fragrance 0.3% Glycerin 5.0% Water 44.7% Total 100.0% The above composition was mixed and dissolved in the same manner as in Example 1, and then allowed to cool to obtain a transparent gel-like facial cleansing composition. Example 3 Facial cleansing composition N-myristoyl-L-aspartic acid dipotassium salt 5.0% Imidazoline-based amphoteric surfactant (-6
Formula) 40.0% Fragrance 0.3% Coconut oil fatty acid diethanolamide 5.0% Water 49.7% Total 100.0% The above compounds were mixed in the same manner as in Example 1, dissolved and then released to obtain a transparent gel facial cleansing composition. . Example 4 Facial cleansing composition N-hardened tallow oil fatty acid acyl-L-glutamic acid monosodium salt 5.0% imidazoline amphoteric surfactant (-7
Formula) 35.0% Sodium N-lauroyl sarcosine 5.0% Fragrance 0.3% Glycerin 5.0% Water 49.7% Total 100.0% The above composition was mixed and dissolved in the same manner as in Example 1, and then allowed to cool to form a transparent gel facial cleanser. A composition was obtained. Example 5 Conditioning shampoo composition N-lauroyl-DL-glutamic acid monosodium salt 10.0% N-oleoyl-DL-aspartic acid monosodium salt 10.0% Imidazoline-based amphoteric surfactant (above-3)
Formula) 40.0% Glycerin 5.0% Cationized cellulose 1.0% Fragrance 0.3% Water 33.7% Total 100.0% The above composition was mixed and dissolved in the same manner as in Example 1, and then allowed to cool to form a transparent gel-like conditioner. A shampoo composition was obtained. The cleaning compositions of Examples 1 to 5 were subjected to storage stability, sensory tests, and skin irritation tests based on the following methods. Storage stability test The condition was visually judged after being left in a constant temperature room at 0°C and 40°C for 2 weeks. ◎: Extremely good transparent gel state ○: Good transparent gel state ×: Devitrification, caking, or liquefaction Sensory test A panel of 30 women aged 18 to 30 was tested on the hands and face for face wash and for shampoo. The number of people who had their hair washed and answered that it was good was displayed. Skin irritation test A 24-hour closed patch test with a 10% aqueous solution of each sample was conducted using 10 New Zealand White male rabbits. Judgment was made according to the Draize method below. Draize method A Erythema and eschar formation No erythema 0 Very slight erythema 1 Clear erythema 2 Moderate to severe erythema 3 Severe erythema (dark red) and slight eschar formation
4 B edema formation No edema 0 Very slight edema 1 Mild edema (clear bulge, clear surroundings) 2 Moderate edema (bulge height approximately 1 mm) 3 Severe edema (bulge height 1 mm or more) 4 Judgment Σ (A+B)÷10 ≦2 Mild 〃 <5 Moderate 〃 ≧5 Severe

【表】 表‐1より明らかなように、本発明の透明ゲル
状洗浄剤は保存安定性が良好で、既知の透明ゲル
状洗浄剤(比較例)に比して優れた起泡力、良好
な使用感を有する。尚、比較例の配合成分は表‐
2に示した。
[Table] As is clear from Table 1, the transparent gel-like cleaning agent of the present invention has good storage stability, and has excellent foaming power and good foaming power compared to the known transparent gel-like cleaning agent (comparative example). It has a feeling of use. The ingredients of the comparative example are shown in the table.
Shown in 2.

【表】【table】

【表】 実施例 6 N‐ヤシ油脂肪酸アシル‐L‐グル タミン酸モノナトリウム塩(A) イミダゾリン系両性界面活性剤 (前記‐1式)(B)50.0% 香 料 0.3% 水 49.7% 計100.0% 上記組成物中に於て、N‐ヤシ油脂肪酸アシ
ル‐L‐グルタミン酸モノナトリウム塩とイミダ
ゾリン系両性界面活性剤の配合比を表‐3の如く
変化させ、実施例1に準じた方法で透明ゲル状洗
浄剤を調製し、評価した。 表‐3の結果より、N‐ヤシ油脂肪酸アシル‐
L‐グルタミン酸モノナトリウムとイミダゾリン
系両性界面活性剤の配合割合が重量比で8/2〜
1/9である場合は保存安定性の良好の透明ゲル
を与えることが了解されよう。
[Table] Example 6 N-coconut oil fatty acid acyl-L-glutamic acid monosodium salt (A) Imidazoline amphoteric surfactant (Formula 1 above) (B) 50.0% Fragrance 0.3% Water 49.7% Total 100.0 % In the above composition, the blending ratio of N-coconut oil fatty acid acyl-L-glutamic acid monosodium salt and imidazoline amphoteric surfactant was changed as shown in Table 3, and transparent was prepared in the same manner as in Example 1. A gel-like cleaning agent was prepared and evaluated. From the results in Table 3, N-coconut oil fatty acid acyl-
The weight ratio of monosodium L-glutamate and imidazoline amphoteric surfactant is 8/2~
It will be understood that a ratio of 1/9 provides a transparent gel with good storage stability.

【表】【table】

【表】 実施例 7 N‐ヤシ油脂肪酸アシル‐L‐グルタミン酸モ
ノナトリウム塩 x% イミダゾリン系両性界面活性剤(前記‐1
式) x% 香 料 0.3%水 (99.7−2x)% 計100.0% 上記粗製物中に於て、N‐ヤシ油脂肪酸アシ
ル‐L‐グルタミン酸ナトリウム塩とイミダゾリ
ン系両性界面活性剤の含有量を表‐4の如く変化
させ、実施例1に準じた方法で透明ゲル状洗浄剤
を調製し、評価した。 その結果を表‐4に示した通り、N‐ヤシ油脂
肪酸アシル‐L‐グルタミン酸ナトリウム塩とイ
ミダゾリン系両性界面活性剤の含有量は40〜70重
量%である場合、透明ゲルが形成する。
[Table] Example 7 N-coco fatty acid acyl-L-glutamic acid monosodium salt x% imidazoline amphoteric surfactant (-1
(Formula) -4, a transparent gel-like cleaning agent was prepared and evaluated in the same manner as in Example 1. As shown in Table 4, a transparent gel was formed when the content of N-coco fatty acid acyl-L-glutamic acid sodium salt and imidazoline amphoteric surfactant was 40 to 70% by weight.

【表】【table】

Claims (1)

【特許請求の範囲】 1 (A)下記一般式()で表わされるアミノ酸系
界面活性剤と(B)下記一般式()で表わされるイ
ミダゾリン系両性界面活性剤と(C)水を必須成分と
する洗剤組成物に於て、(A)成分と(B)成分との割合
(A)/(B)が、重量比で8/2〜1/9であり、かつ
界面活性剤濃度を40〜70重量%の範囲に調整して
なる透明ゲル状洗浄剤組成物。 (但し、R1は炭素数7〜21のアルキル基または
アルケニル基、M1,M2はそれぞれ水素原子また
はアルカリ金属、nは1または2の整数を示す。) (但し、R2は炭素数7〜21のアルキル基または
アルケニル基、R3は水素原子、アルカリ金属ま
たは CH2COOM3、ZはCOOM3,CH2COOM3または 【式】M3は水素原子、アルカリ 金属またはアルカノールアミンを示す。)
[Claims] 1. (A) an amino acid surfactant represented by the following general formula (), (B) an imidazoline amphoteric surfactant represented by the following general formula (), and (C) water as essential components. The ratio of component (A) to component (B) in the detergent composition
A transparent gel-like cleaning composition having a weight ratio of (A)/(B) of 8/2 to 1/9 and a surfactant concentration adjusted to a range of 40 to 70% by weight. (However, R 1 is an alkyl group or alkenyl group having 7 to 21 carbon atoms, M 1 and M 2 are each a hydrogen atom or an alkali metal, and n is an integer of 1 or 2.) (However, R 2 is an alkyl group or alkenyl group having 7 to 21 carbon atoms, R 3 is a hydrogen atom, an alkali metal or CH 2 COOM 3 , Z is COOM 3 , CH 2 COOM 3 or [Formula] M 3 is a hydrogen atom , indicating an alkali metal or alkanolamine).
JP10531483A 1983-06-13 1983-06-13 Transparent gel-like detergent composition Granted JPS59230099A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP10531483A JPS59230099A (en) 1983-06-13 1983-06-13 Transparent gel-like detergent composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP10531483A JPS59230099A (en) 1983-06-13 1983-06-13 Transparent gel-like detergent composition

Publications (2)

Publication Number Publication Date
JPS59230099A JPS59230099A (en) 1984-12-24
JPH0433839B2 true JPH0433839B2 (en) 1992-06-04

Family

ID=14404239

Family Applications (1)

Application Number Title Priority Date Filing Date
JP10531483A Granted JPS59230099A (en) 1983-06-13 1983-06-13 Transparent gel-like detergent composition

Country Status (1)

Country Link
JP (1) JPS59230099A (en)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2695448B2 (en) * 1988-09-28 1997-12-24 三菱化学株式会社 Liquid detergent composition
JPH02268114A (en) * 1989-04-07 1990-11-01 Mitsubishi Petrochem Co Ltd Detergent composition of good rinsing properties
JP7338471B2 (en) 2017-11-06 2023-09-05 味の素株式会社 detergent composition

Also Published As

Publication number Publication date
JPS59230099A (en) 1984-12-24

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