JPS6220596A - Liquid detergent composition - Google Patents
Liquid detergent compositionInfo
- Publication number
- JPS6220596A JPS6220596A JP15894185A JP15894185A JPS6220596A JP S6220596 A JPS6220596 A JP S6220596A JP 15894185 A JP15894185 A JP 15894185A JP 15894185 A JP15894185 A JP 15894185A JP S6220596 A JPS6220596 A JP S6220596A
- Authority
- JP
- Japan
- Prior art keywords
- general formula
- fatty acid
- formula
- acid
- saturated
- 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.)
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Abstract
(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.
Description
【発明の詳細な説明】
1吐へ札」矩1
本発明は、優れた洗浄性能と泡安定性を備え、皮膚に対
して温和でかつ保存安定性の良好な液体洗浄剤組成物に
関するものである。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a liquid detergent composition that has excellent cleaning performance and foam stability, is mild to the skin, and has good storage stability. be.
l1へ11
近年、台所用洗剤およびシャンプーに求められる性能と
しては、優れた洗浄力や起泡力の他に、低毒性であるこ
とはもちろん皮膚に対して温和であることが重要である
。このような諸性能を満足する洗浄剤組成物として、例
えばN−アシルアミノ酸系界面活性剤とアルキルジメチ
ルアミンオキサイドなどのアミンオキサイド型界面活性
剤からなる液体洗浄剤組成物く特開昭48−55904
号)が知られている。11 In recent years, in addition to excellent cleaning power and foaming power, the performance required for kitchen detergents and shampoos is not only low toxicity but also mildness to the skin. As a detergent composition that satisfies these various performances, for example, a liquid detergent composition comprising an N-acyl amino acid surfactant and an amine oxide type surfactant such as an alkyldimethylamine oxide is disclosed in Japanese Patent Application Laid-Open No. 48-55904.
No.) is known.
しかしながら、N−アシルサルコシン塩やN−アシルグ
ルタミン酸塩のようなN−アシルアミノ酸系界面活性剤
とアルキルアミンオキサイドとを組み合わせると、しば
しば低温安定性や相溶性が悪化して濁りが発生するため
、洗浄剤としての商品価値を著しく損ねることが多かっ
た。そこでこのような欠点を改良するために、配合割合
の変更や親水性溶媒やハイドロトロープ等の添加を必要
とし、N−アシルアミノ酸系界面活性剤やアルキルアミ
ンオキサイドの特性を生かすことができなかった。However, when N-acyl amino acid surfactants such as N-acyl sarcosine salts and N-acyl glutamates are combined with alkylamine oxides, low-temperature stability and compatibility often deteriorate and turbidity occurs. In many cases, the product value as a cleaning agent was significantly impaired. Therefore, in order to improve these drawbacks, it was necessary to change the blending ratio or add hydrophilic solvents, hydrotropes, etc., and it was not possible to take advantage of the characteristics of N-acylamino acid surfactants and alkylamine oxides. .
日(゛。Day (゛.
本発明は、N−アシルアミノ酸系界面活性剤とアミンオ
キサイド型界面活性剤との組合わせにおいて、低温安定
性などの保存安定性が良好で、優れた洗浄力と起泡力を
備えかつ皮膚に対しても温和な洗浄剤組成物を提供する
ことにある。The present invention provides a combination of an N-acyl amino acid surfactant and an amine oxide surfactant that has good storage stability such as low temperature stability, excellent detergency and foaming power, and is gentle on the skin. It is an object of the present invention to provide a cleaning composition that is gentle even for people with disabilities.
a ゛ るt・めの
上記問題点は、アミンオキサイド型界面活性剤として特
定のアミドアミンオキサイドを選択し、これにN−アシ
ルアミノ酸系界面活性剤とアルカノールアミドを配合す
ることにより解決される。The above-mentioned problems can be solved by selecting a specific amidoamine oxide as the amine oxide type surfactant and blending it with an N-acylamino acid type surfactant and an alkanolamide.
すなわち本発明は、下記(A)、(B)および(C)の
三成分からなることを特徴とする液体洗浄剤組成物に関
するものである。That is, the present invention relates to a liquid cleaning composition characterized by comprising the following three components (A), (B), and (C).
(A>一般式(I)
RICONH(CH2)3 N→0 (■ )く
ただし、式中R,COは、炭素数10ないし20の飽和
または不飽和の脂肪酸残基、R2およびR3はメチル基
、エチル基またはヒドロキシエチル基を表す)
で示されるアミドアミンオキサイド1.5ないし15重
量%
(B)一般式(II)
CH3
曙
R4CON CH2COOM s (n
)(式中、R4C0は、炭素数10ないし20の飽和
または不飽和の脂肪酸残基、Mはアルカリ金属、アンモ
ニウム、アルカノールアミンまたは塩基性アミノ酸の陽
イオン残基がら選ばれる少なくとも1種を表す)
で示されるN−アシルサルコシン塩および一般式(II
I)
(式中、R5Coは、炭素数10ないし20の飽和また
は不飽和の脂肪酸残基、M2およびM3は水素原子、ア
ルカリ金属、アンモニウム、アルカノールアミンまたは
塩基性アミノ酸の陽イオン残基から選ばれる少なくとも
1種を表す)で示されるN−アシルグルタミン酸塩から
選ばれる少なくとも1種のN−アシルアミノ酸塩1.5
ないし30重量%
(C)一般式(IV)
(式中R6C○は、炭素数10ないし20の飽和または
不飽和の脂肪酸残基、mは1ないし20の整数、nはO
ないし20の整数を表す)で示されるアルカノールアミ
ド1.0ないし10重量%
本発明で用いられる第一成分のアミドアミンオキサイド
は前記一般式(I>で示される化合物であり、式中のR
,CO基となりうる脂肪酸残基としては、ラウリン酸、
ミリスチン酸、パルミチン酸、オレイン酸、ステアリン
酸、イソステアリン酸、ヤシ油脂肪酸、ヒマシ油脂肪酸
、牛脂脂肪酸、ナタネ油脂肪酸などの脂肪酸の残基があ
げられる。(A>General formula (I) RICONH(CH2)3 N→0 (■) However, in the formula, R and CO are saturated or unsaturated fatty acid residues having 10 to 20 carbon atoms, and R2 and R3 are methyl groups. , ethyl group or hydroxyethyl group) (B) General formula (II) CH3 Akebono R4CON CH2COOM s (n
) (wherein, R4C0 represents a saturated or unsaturated fatty acid residue having 10 to 20 carbon atoms, and M represents at least one selected from cationic residues of alkali metals, ammonium, alkanolamines, and basic amino acids) N-acyl sarcosine salts represented by and general formula (II
I) (wherein R5Co is a saturated or unsaturated fatty acid residue having 10 to 20 carbon atoms, M2 and M3 are selected from hydrogen atoms, alkali metals, ammonium, alkanolamines, or cationic residues of basic amino acids) At least one N-acyl amino acid salt selected from N-acyl glutamic acid salts represented by
to 30% by weight (C) General formula (IV) (wherein R6C○ is a saturated or unsaturated fatty acid residue having 10 to 20 carbon atoms, m is an integer of 1 to 20, and n is O
1.0 to 10% by weight of alkanolamide represented by the formula (representing an integer from 20 to 20) The amidoamine oxide as the first component used in the present invention is a compound represented by the general formula (I>), in which R
, fatty acid residues that can become CO groups include lauric acid,
Examples include residues of fatty acids such as myristic acid, palmitic acid, oleic acid, stearic acid, isostearic acid, coconut oil fatty acid, castor oil fatty acid, beef tallow fatty acid, and rapeseed oil fatty acid.
このような一般式<I)のアミンオキサイドの代表的な
化合物としては、ラウラミドブロビルジメチルアミンオ
キサイド、オレアミドプロピルジメチルアミンオキサイ
ド、ココ(ヤシ油脂肪酸アシル)アミドプロピルジメチ
ルアミンオキサイドなどが挙げられる。Representative compounds of such amine oxides of the general formula <I) include lauramidobrobyl dimethylamine oxide, oleamidopropyl dimethylamine oxide, coco (coconut oil fatty acid acyl) amidopropyl dimethylamine oxide, etc. .
一般式(I)のアミドアミンオキサイドの製造方法はと
くに限定されないが、たとえば、ラウリン酸などの脂肪
酸またはその低級アルキルエステルとジメチルアミンプ
ロピルアミンとを縮合して得られるアミドアミン化合物
に過酸化水素を反応させる方法かある。The method for producing amidoamine oxide of general formula (I) is not particularly limited, but for example, hydrogen peroxide is reacted with an amidoamine compound obtained by condensing a fatty acid such as lauric acid or its lower alkyl ester with dimethylamine propylamine. There is a way.
本発明で用いられる第二成分のN−アシルアミノ酸型界
面活性剤は、前記一般式(II)および/または(1)
で示されるN−アシルサルコシン塩、N−アシルグルタ
ミン酸塩である。アシル基としては、ラウリン酸、ミリ
スチン酸、パルミチン酸、オレイン酸、ステアリン酸、
イソステアリン酸、ヤシ油脂肪酸、牛脂脂肪酸、ヒマシ
油脂肪酸、ナタネ油脂肪酸などの脂肪酸の残基があげら
れる。The second component N-acyl amino acid type surfactant used in the present invention has the general formula (II) and/or (1).
N-acyl sarcosine salt and N-acyl glutamate represented by Acyl groups include lauric acid, myristic acid, palmitic acid, oleic acid, stearic acid,
Examples include residues of fatty acids such as isostearic acid, coconut oil fatty acid, beef tallow fatty acid, castor oil fatty acid, and rapeseed oil fatty acid.
N−アシルアミノ酸塩の塩としては、ナトリウム塩やカ
リウム塩などのアルカリ金属塩、アンモニウム塩、モノ
エタノールアミン塩やトリエタノールアミン塩などのア
ルカノールアミン塩、リジン塩などの塩基性アミノ酸塩
などがあげられる。Examples of N-acyl amino acid salts include alkali metal salts such as sodium salts and potassium salts, ammonium salts, alkanolamine salts such as monoethanolamine salts and triethanolamine salts, and basic amino acid salts such as lysine salts. It will be done.
本
発明の第三成分として用いられるアルカノールアミドは
前記一般式(IV)で示される化合物であり、式中のR
6C0基となりうる脂肪酸残基としては、ラウリン酸、
ミリスチン酸、パルミチン酸、オレイン酸、ステアリン
酸、イソステアリン酸、ヤシ油脂肪酸、牛脂脂肪酸、ヒ
マシ油脂肪酸、ナタネ油脂肪酸などの脂肪酸の残基があ
げられる。一般式(IV)のmは実用上1ないし10が
好ましく、nは0ないし20が好ましい。The alkanolamide used as the third component of the present invention is a compound represented by the above general formula (IV), in which R
Fatty acid residues that can become 6C0 groups include lauric acid,
Examples include residues of fatty acids such as myristic acid, palmitic acid, oleic acid, stearic acid, isostearic acid, coconut oil fatty acid, beef tallow fatty acid, castor oil fatty acid, and rapeseed oil fatty acid. In general formula (IV), m is practically preferably 1 to 10, and n is preferably 0 to 20.
本発明における各成分の配合割合は前記のとおりであり
、各成分が配合割合の範囲をこえると下記のような欠点
が生じ好ましくない。The blending ratio of each component in the present invention is as described above, and if each component exceeds the range of the blending ratio, the following disadvantages occur, which is not preferable.
すなわち、第一成分のアミドアミンオキサイドが1.5
重量%未満では泡たち、洗浄力および保存安定性が劣り
、また15重量%を超えると洗浄剤の粘性が急激に高く
なり粘度コントロールが困難となる。That is, the first component, amidoamine oxide, is 1.5
If it is less than 15% by weight, the foaming, detergency and storage stability will be poor, and if it exceeds 15% by weight, the viscosity of the detergent will increase rapidly and it will be difficult to control the viscosity.
第二成分のN−アシルアミノ酸塩の配合割合が1.5重
量%未満では洗浄力が劣り、30重1%を超えると保存
安定性が低下する。If the blending ratio of the second component, N-acylamino acid salt, is less than 1.5% by weight, the cleaning power will be poor, and if it exceeds 30% by weight, the storage stability will be reduced.
第三成分であるアルカノールアミドの配合割合が1.0
重量%未満では増粘、増泡効果が期待できず、10重量
%を超えると保存安定性が低下し、かつ洗浄剤の粘度が
急激に高くなり粘度コントロールが困難となる。The blending ratio of the third component, alkanolamide, is 1.0.
If it is less than 10% by weight, thickening and foaming effects cannot be expected, and if it exceeds 10% by weight, the storage stability will decrease and the viscosity of the detergent will increase rapidly, making it difficult to control the viscosity.
本発明の目的を損なわない限り、他の陰イオン界面活性
剤、非イオン界面活性剤、両性界面活性剤や、洗浄剤組
成物に常用されている色素、香料、ハイドロトロープ、
金属イオン封鎖剤、防菌剤、保湿剤等の補助剤を添加し
てもよい。Unless the purpose of the present invention is impaired, other anionic surfactants, nonionic surfactants, amphoteric surfactants, pigments, fragrances, hydrotropes, etc. commonly used in cleaning compositions,
Auxiliary agents such as metal ion sequestering agents, antibacterial agents, and humectants may be added.
1皿
本発明の液体洗浄剤組成物の保存安定性が向上している
のは、アミドアミンオキサイドとN−アシルアミノ酸塩
とアルカノールアミドの三成分の相乗効果によるものと
思われるが、詳細な理由は不明である。The storage stability of the liquid detergent composition of the present invention is improved due to the synergistic effect of the three components: amidoamine oxide, N-acyl amino acid salt, and alkanolamide, but the detailed reason is It is unknown.
火」L医」二二j−1比較例1〜7
第1表に示す組成割合の界面活性剤を蒸留水に溶解し、
pHをクエン酸で6.0として、本発明の洗浄剤と比較
例の洗浄剤を調製し、これらの保存安定性を調べた。な
お、表中の各成分の数値は重量%を表す。Fire "L Doctor" 22j-1 Comparative Examples 1 to 7 A surfactant having the composition ratio shown in Table 1 was dissolved in distilled water,
A cleaning agent of the present invention and a cleaning agent of a comparative example were prepared by adjusting the pH to 6.0 with citric acid, and their storage stability was investigated. In addition, the numerical value of each component in a table|surface represents weight%.
洗浄剤の粘度は、B型粘度計を用いて測定し、保存安定
性として、次の低温安定性試験と高温安定性試験を行っ
た。The viscosity of the cleaning agent was measured using a B-type viscometer, and the following low-temperature stability test and high-temperature stability test were conducted to check storage stability.
(低温安定性試験)
洗浄剤を試験管に入れ、−5°Cの恒温槽に3日間保存
したときの外観を肉眼で観察した。(Low temperature stability test) The detergent was placed in a test tube and stored in a -5°C constant temperature bath for 3 days, and its appearance was observed with the naked eye.
(高温安定性試験)
洗浄剤を100ccの透明ビンに入れ、50°C恒温槽
に1ケ月間保存したときの外観を肉眼で観察した。(High-temperature stability test) The detergent was placed in a 100 cc transparent bottle and stored in a 50°C constant temperature bath for one month, and its appearance was visually observed.
(判定基準)
低温安定性および高温安定性は次の基準によって評価し
た。(Judgment Criteria) Low-temperature stability and high-temperature stability were evaluated according to the following criteria.
O・・・・・・透明液 △・・・・・・不透
明液×・・・・・・白濁または分離液
以下余白
第1表の結果から、本発明の液体洗浄剤組成物は保存安
定性に優れ、しかも粘度コントロールが容易であるのに
対して、比較例の洗浄剤は保存安定性が悪いか粘度コン
トロールが困難(極端に低いかまたは高すぎてゲル状に
なつしよう)であることが明らかである。O: Transparent liquid △: Opaque liquid ×: Cloudy or separated liquid From the results in Table 1, the liquid cleaning composition of the present invention has storage stability. In contrast, the detergents in the comparative examples had poor storage stability or difficulty in controlling the viscosity (either extremely low or too high, resulting in a gel-like state). it is obvious.
実施例6〜10、比較例8〜12
第2表に示す組成で実施例1に準じて洗浄剤を調製し、
これらの粘度と保存安定性を調べた。なお、表中の各成
分の数値は重量%を表す。Examples 6 to 10, Comparative Examples 8 to 12 Cleaning agents were prepared according to Example 1 with the compositions shown in Table 2,
Their viscosity and storage stability were investigated. In addition, the numerical value of each component in a table|surface represents weight%.
洗浄剤の粘度と保存安定性は実施例1に準じて測定した
。The viscosity and storage stability of the detergent were measured according to Example 1.
以下余白
第2表の結果から、本発明の液体洗浄剤組成物は保存安
定性に優れ、しかも粘度コントロールが容易であるのに
対して、比較例の洗浄剤は保存安定性か悪いか粘度コン
トロールが困難(i端に低いかまたは高すぎてゲル状に
なっしまう)であることが明らかである。From the results in Table 2 in the margin below, it can be seen that the liquid cleaning composition of the present invention has excellent storage stability and is easy to control viscosity, whereas the cleaning agent of the comparative example has poor storage stability or viscosity control. It is clear that it is difficult (low or too high at the i-end, resulting in a gel-like state).
実施例11 (シャンプー)
・ラウラミドプロピルジメチルー %アミン
オキサイド 5.0・N−ココイ
ルサルコシン−
トリエタノールアミン塩 8,0・N−
タロイルグルタミン酸モノナトリーウム塩
3.0・ラウリン酸モノエタノール
アミド−
ポリエトキシレート
(E○平均付加モル数10) 3.0・クエ
ン酸 p H7,0とする量・
バランス100.0
実施例12 (シャンプー)
・パルミタアミドブロピルジエチルー %アミン
オキサイド 2.0・N−オレオ
イルサルコシンリジン塩 4.5・ヤシ油脂肪酸酸ジ
ェタノールアミド 3.0・ラウリルアルコール硫酸
エステル−
ナトリウム 3.0・クエ
ン酸 p H6,0とする量・
バーンス100.0
実施例13(シャンプー)
・ココアミドプロピルジエチルアミン−%オキサイド
5.0・N−ラウロイルグル
タミン酸モノ
トリエタノールアミン塩 10.0・ラウリ
ン酸ジェタノールアミド 3.0・α−オレフィ
ンスルホン酸ナトリウム 3.0・クエン酸
pH7,0とする量・エデト酸2ナトリウム塩
0.1・
バランス100.0
上記実施例11〜13で得られたシャンプーは保存安定
性が良好で、泡たち、洗浄性とも優れ、目に対する刺激
が少ないことが認められた。Example 11 (Shampoo) Lauramidopropyl dimethyl % Amine oxide 5.0 N-cocoylsarcosine Triethanolamine salt 8,0 N-
Taloylglutamate monosodium salt
3.0・Lauric acid monoethanolamide-polyethoxylate (E○ average number of added moles 10) 3.0・Citric acid Amount to make pH 7.0・
Balance 100.0 Example 12 (Shampoo) ・Palmitamidobropyrdiethyl % Amine oxide 2.0 ・N-oleoylsarcosine lysine salt 4.5 ・Coconut oil fatty acid acid jetanolamide 3.0 ・Lauryl alcohol sulfuric acid Ester - Sodium 3.0 Citric acid Amount to make pH 6.0
Burns 100.0 Example 13 (Shampoo) Cocoamidopropyl diethylamine-% oxide
5.0 N-lauroylglutamic acid monotriethanolamine salt 10.0 Lauric acid jetanolamide 3.0 Sodium α-olefin sulfonate 3.0 Citric acid
Amount to adjust pH to 7.0・edetate disodium salt 0.1・
Balance: 100.0 It was found that the shampoos obtained in Examples 11 to 13 had good storage stability, excellent lathering and cleansing properties, and little irritation to the eyes.
実施例14(台所洗剤)
・牛脂アミドプロピルジメチル−%
アミンオキサイド 2.0・ココア
ミドプロピルビス(2−ヒトローキシエチル)アミンオ
キサイド 2.0・N−オレイルグルタミン酸
ジナトリウム塩 5.5・ポリオ
キシエチレンラウリルエーテル−サルフェートナトリウ
ム
(EO平均付加モル数5) 8.5・ヤシ
油脂肪酸モノエタノールアミド−ポリエトキシレート
(EO平均付加モル数5) 2.0・エタ
ノール 3.0・
65.0100.0
上記台所洗剤は、優れた低温安定性を示し、また台所洗
剤としての泡たち、洗浄力も良好であることが認められ
た。Example 14 (Dish detergent) - Beef tallow amidopropyl dimethyl - % Amine oxide 2.0 - Cocoamidopropyl bis(2-hydroxyethyl) amine oxide 2.0 - N-oleylglutamic acid disodium salt 5.5 - Poly Oxyethylene lauryl ether-sodium sulfate (EO average number of moles added 5) 8.5 Coconut oil fatty acid monoethanolamide polyethoxylate (EO average number of moles added 5) 2.0 Ethanol 3.0
65.0100.0 The above kitchen detergent was found to exhibit excellent low-temperature stability and to have good foaming and detergency as a kitchen detergent.
実施例15 (ハンドクリーナー) %・α−
オレフィンスルホン酸ナトリウム 8.0・ココアミド
プロピルジメチルアミン−オキサイド
2.0・N−ココイルサルコシンナトリウム
塩 5.0・硬化牛脂脂肪酸モノエタノールアミド−ポ
リエトキシレート
(EO平均付加モル数10) 2.0・クエ
ン酸 pH6,5とする量・
バーンス100.0
上記ハンドクリーナーは粘稠な透明液体で、優れた低温
安定性を示し、またハンドクリーナーとしての泡たち、
洗浄力に優れ、皮膚に対する刺激も少ないことが認めら
れた。Example 15 (Hand cleaner) %・α-
Sodium olefin sulfonate 8.0 Cocoamidopropyl dimethylamine oxide
2.0・N-cocoylsarcosine sodium salt 5.0・Hardened beef tallow fatty acid monoethanolamide polyethoxylate (EO average added mole number 10) 2.0・Citric acid Amount to adjust pH to 6.5・
Burns 100.0 The above hand cleaner is a viscous transparent liquid, exhibits excellent low temperature stability, and has foam as a hand cleaner.
It was found to have excellent cleaning power and less irritation to the skin.
1iユ11
本発明の液体洗浄剤組成物は以下のような優れた特徴を
有する。1iyu11 The liquid cleaning composition of the present invention has the following excellent characteristics.
(1)低温および高温における保存安定性が良好である
。(1) Good storage stability at low and high temperatures.
に)優れた洗浄力と起泡力を備え、かつ皮膚に対しても
温和である。2) It has excellent cleaning and foaming power, and is gentle on the skin.
Claims (1)
ことを特徴とする液体洗浄剤組成物。 (A)一般式( I ) ▲数式、化学式、表等があります▼( I ) (ただし、式中R_1COは、炭素数10ないし20の
飽和または不飽和の脂肪酸残基、R_2およびR_3は
メチル基、エチル基またはヒドロキシエチル基を表す) で示されるアミドアミンオキサイド1.5ないし15重
量% (B)一般式(II) ▲数式、化学式、表等があります▼(II) (式中、R_4COは、炭素数10ないし20の飽和ま
たは不飽和の脂肪酸残基、Mはアルカリ金属、アンモニ
ウム、アルカノールアミンまたは塩基性アミノ酸の陽イ
オン残基から選ばれる少なくとも1種を表す) で示されるN−アシルサルコシン塩および一般式(III
) ▲数式、化学式、表等があります▼(III) (式中、R_5COは、炭素数10ないし20の飽和ま
たは不飽和の脂肪酸残基、M_2およびM_3は水素原
子、アルカリ金属、アンモニウム、アルカノールアミン
または塩基性アミノ酸の陽イオン残基から選ばれる少な
くとも1種を表す) で示されるN−アシルグルタミン酸塩から選ばれる少な
くとも1種のN−アシルアミノ酸塩1.5ないし30重
量% (C)一般式(IV) ▲数式、化学式、表等があります▼(IV) (式中R_6COは、炭素数10ないし20の飽和また
は不飽和の脂肪酸残基、mは1ないし20の整数、nは
0ないし20の整数を表す) で示されるアルカノールアミド1.0ないし10重量% 2、一般式( I )のR_2およびR_3がそれぞれメ
チル基である特許請求の範囲第1項記載の組成物。 3、一般式(II)のM_1がナトリウムである特許請求
の範囲第1項記載の組成物。 4、一般式(III)のM_2および/またはM_3がナ
トリウムである特許請求の範囲第1項記載の組成物。[Scope of Claims] 1. A liquid detergent composition comprising the following three components (A), (B) and (C). (A) General formula (I) ▲Mathematical formulas, chemical formulas, tables, etc.▼(I) (However, in the formula, R_1CO is a saturated or unsaturated fatty acid residue having 10 to 20 carbon atoms, and R_2 and R_3 are methyl groups. , ethyl group or hydroxyethyl group) 1.5 to 15% by weight of amidoamine oxide represented by (B) General formula (II) ▲ Numerical formula, chemical formula, table, etc. ▼ (II) N-acylsarcosine salt represented by a saturated or unsaturated fatty acid residue having 10 to 20 carbon atoms, M representing at least one selected from cationic residues of alkali metals, ammonium, alkanolamines, or basic amino acids. and general formula (III
) ▲Mathematical formulas, chemical formulas, tables, etc.▼(III) (In the formula, R_5CO is a saturated or unsaturated fatty acid residue with 10 to 20 carbon atoms, M_2 and M_3 are hydrogen atoms, alkali metals, ammonium, alkanolamines 1.5 to 30% by weight of at least one N-acyl amino acid salt selected from N-acyl glutamic acid salts represented by (C) General formula (IV) ▲There are mathematical formulas, chemical formulas, tables, etc.▼ (IV) (In the formula, R_6CO is a saturated or unsaturated fatty acid residue having 10 to 20 carbon atoms, m is an integer from 1 to 20, and n is 0 to 20. 2. The composition according to claim 1, wherein R_2 and R_3 of the general formula (I) are each a methyl group. 3. The composition according to claim 1, wherein M_1 in general formula (II) is sodium. 4. The composition according to claim 1, wherein M_2 and/or M_3 in general formula (III) is sodium.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP15894185A JPS6220596A (en) | 1985-07-18 | 1985-07-18 | Liquid detergent composition |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP15894185A JPS6220596A (en) | 1985-07-18 | 1985-07-18 | Liquid detergent composition |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS6220596A true JPS6220596A (en) | 1987-01-29 |
JPH0580520B2 JPH0580520B2 (en) | 1993-11-09 |
Family
ID=15682685
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP15894185A Granted JPS6220596A (en) | 1985-07-18 | 1985-07-18 | Liquid detergent composition |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS6220596A (en) |
Cited By (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH02180811A (en) * | 1988-12-29 | 1990-07-13 | Kanebo Ltd | Transparent gelatinous cleaning agent for skin |
FR2705673A1 (en) * | 1993-05-25 | 1994-12-02 | Givaudan Lavirotte | Compositions comprising amino acid derivatives, methods for their preparation and uses thereof |
WO1995033811A1 (en) * | 1994-06-02 | 1995-12-14 | The Procter & Gamble Company | Oleoyl sarcosinate with alkanolamides in cleaning products |
USH1514H (en) * | 1994-06-01 | 1996-01-02 | The Procter & Gamble Company | Detergent compositions with oleoyl sarcosinate and polymeric dispersing agent |
USH1513H (en) * | 1994-06-01 | 1996-01-02 | The Procter & Gamble Company | Oleoyl sarcosinate with polyhydroxy fatty acid amides in cleaning products |
USH1635H (en) * | 1994-06-01 | 1997-03-04 | The Procter & Gamble Company | Detergent compositions with oleoyl sarcosinate and amine oxide |
JPH10176187A (en) * | 1996-12-18 | 1998-06-30 | Kao Corp | Detergent composition for hard surface |
JPH11114400A (en) * | 1997-10-20 | 1999-04-27 | Kao Corp | Cationic emulsifier for asphalt emulsion |
US6095161A (en) * | 1997-01-17 | 2000-08-01 | Micron Technology, Inc. | Processing and post-processing compositions and methods of using same |
JP2000219668A (en) * | 1999-01-28 | 2000-08-08 | Kawaken Fine Chem Co Ltd | Amidoamine oxide-type surface active compound and surfactant |
JP2002212599A (en) * | 2001-01-12 | 2002-07-31 | Kawaken Fine Chem Co Ltd | Liquid detergent composition |
JP2010083903A (en) * | 2002-05-31 | 2010-04-15 | Kao Corp | Agricultural chemical composition |
JP2019034915A (en) * | 2017-08-21 | 2019-03-07 | 株式会社ファンケル | Liquid cleaning composition |
-
1985
- 1985-07-18 JP JP15894185A patent/JPS6220596A/en active Granted
Cited By (16)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH02180811A (en) * | 1988-12-29 | 1990-07-13 | Kanebo Ltd | Transparent gelatinous cleaning agent for skin |
FR2705673A1 (en) * | 1993-05-25 | 1994-12-02 | Givaudan Lavirotte | Compositions comprising amino acid derivatives, methods for their preparation and uses thereof |
WO1994027561A1 (en) * | 1993-05-25 | 1994-12-08 | Givaudan-Lavirotte | Compositions comprising amino acid derivatives, their methods of preparation and use |
USH1514H (en) * | 1994-06-01 | 1996-01-02 | The Procter & Gamble Company | Detergent compositions with oleoyl sarcosinate and polymeric dispersing agent |
USH1513H (en) * | 1994-06-01 | 1996-01-02 | The Procter & Gamble Company | Oleoyl sarcosinate with polyhydroxy fatty acid amides in cleaning products |
USH1635H (en) * | 1994-06-01 | 1997-03-04 | The Procter & Gamble Company | Detergent compositions with oleoyl sarcosinate and amine oxide |
WO1995033811A1 (en) * | 1994-06-02 | 1995-12-14 | The Procter & Gamble Company | Oleoyl sarcosinate with alkanolamides in cleaning products |
JPH10176187A (en) * | 1996-12-18 | 1998-06-30 | Kao Corp | Detergent composition for hard surface |
US6095161A (en) * | 1997-01-17 | 2000-08-01 | Micron Technology, Inc. | Processing and post-processing compositions and methods of using same |
JPH11114400A (en) * | 1997-10-20 | 1999-04-27 | Kao Corp | Cationic emulsifier for asphalt emulsion |
JP2000219668A (en) * | 1999-01-28 | 2000-08-08 | Kawaken Fine Chem Co Ltd | Amidoamine oxide-type surface active compound and surfactant |
JP4544657B2 (en) * | 1999-01-28 | 2010-09-15 | 川研ファインケミカル株式会社 | Amidoamine oxide type surface active compound and surfactant |
JP2002212599A (en) * | 2001-01-12 | 2002-07-31 | Kawaken Fine Chem Co Ltd | Liquid detergent composition |
JP4656733B2 (en) * | 2001-01-12 | 2011-03-23 | 川研ファインケミカル株式会社 | Liquid detergent composition |
JP2010083903A (en) * | 2002-05-31 | 2010-04-15 | Kao Corp | Agricultural chemical composition |
JP2019034915A (en) * | 2017-08-21 | 2019-03-07 | 株式会社ファンケル | Liquid cleaning composition |
Also Published As
Publication number | Publication date |
---|---|
JPH0580520B2 (en) | 1993-11-09 |
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