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JPH04114100A - Detergent composition - Google Patents

Detergent composition

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Publication number
JPH04114100A
JPH04114100A JP23614090A JP23614090A JPH04114100A JP H04114100 A JPH04114100 A JP H04114100A JP 23614090 A JP23614090 A JP 23614090A JP 23614090 A JP23614090 A JP 23614090A JP H04114100 A JPH04114100 A JP H04114100A
Authority
JP
Japan
Prior art keywords
alkyl
formula
general formula
cleaning
skin
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.)
Granted
Application number
JP23614090A
Other languages
Japanese (ja)
Other versions
JP2744516B2 (en
Inventor
Akira Utsuki
彰 宇津木
Hideaki Niwase
庭瀬 英明
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.)
Kanebo Ltd
Original Assignee
Kanebo 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 Kanebo Ltd filed Critical Kanebo Ltd
Priority to JP23614090A priority Critical patent/JP2744516B2/en
Publication of JPH04114100A publication Critical patent/JPH04114100A/en
Application granted granted Critical
Publication of JP2744516B2 publication Critical patent/JP2744516B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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  • Detergent Compositions (AREA)

Abstract

PURPOSE:To obtain the subject composition having excellent and detergency with extremely low irritation to skin and hair and having fresh using feeling comprising respectively specific N-acyl aspartic acid salt and alkyl glycoside. CONSTITUTION:The aimed composition contains (A) N-acyl aspartic acid salt expressed by formula I (R1 is 7-21C alkyl or alkenyl; M1 and M2 are H, Na<+>, K<+>, NH4<+> or cation derived from alkanolamine with a proviso that M1 and M2 are not simultaneously H) and (B) alkyl glycoside expressed by formula II (R2 is 8-18C alkyl or alkenyl; G is 5-6C group derived from reduced sugar; n is integer of 1-5) preferably in a weight ratio of the components A/B=0.1-10 and in a total weight of 5-30wt.%.

Description

【発明の詳細な説明】 〔産業上の利用分野〕 本発明は陰イオン界面活性剤及び非イオン界面活性剤を
含有し頭髪用もしくはボディンヤンプー衣類1食器用洗
剤等に用いられ、起泡性、洗浄性に傍れかつ皮膚及び毛
髪に対する刺激が著しく低く又、使用時および使用後に
皮膚にさっばりとした感触を与える洗浄剤組成物に関す
る。
Detailed Description of the Invention [Industrial Field of Application] The present invention contains an anionic surfactant and a nonionic surfactant and is used in detergents for hair or laundry, dishwashing, etc. The present invention relates to a cleansing composition that has good properties in terms of cleansing properties, has extremely low irritation to the skin and hair, and gives a refreshing feel to the skin during and after use.

〔従来の技術〕[Conventional technology]

従来より、頭髪、身体、衣類1食器用の洗浄剤の主剤と
してアルキル硫酸塩、α−オレフィンスルホン酸塩等が
広く使用されている。しかしこれらのアニオン界面活性
剤は、洗浄力には優れているものの、泡質においてリッ
チ惑に欠けまた、皮膚刺激性が強いという問題があった
BACKGROUND ART Conventionally, alkyl sulfates, α-olefin sulfonates, and the like have been widely used as main ingredients for detergents for hair, body, clothing, and tableware. However, although these anionic surfactants have excellent detergency, they lack a rich foam quality and are highly irritating to the skin.

その為近年、本発明の(A)成分であるN−アシルアス
パラギン酸塩を初めとする、N−長鎖アシル酸性アミノ
酸塩が、皮膚や目に対する刺激の少ないシャンプー基材
として注目を集めている。しかしこれらは、ポリオキシ
エチレンアルキルエーテル6A Mエステル塩等と比較
すると、起泡力や洗浄力が劣るものである。
Therefore, in recent years, N-long chain acyl acidic amino acid salts, including N-acylaspartate, which is the component (A) of the present invention, have attracted attention as shampoo base materials that are less irritating to the skin and eyes. . However, these have inferior foaming power and detergency when compared to polyoxyethylene alkyl ether 6AM ester salts and the like.

一方(B)成分のアルキルグリコシドもまた、低刺激性
ではあるものの、起泡力、洗浄力に劣るという欠点が見
られる。
On the other hand, although the alkyl glycoside of component (B) is also hypoallergenic, it has the disadvantage of being inferior in foaming power and detergency.

そこで特開平1−178597において、Nアシルグル
タミン酸塩や、N−アノルアラニン塩と、アルキルグリ
コンドを配合した、低刺激性かつ起泡力にも冨み泡質の
リッチ感に優れた洗浄剤組成物が提案されている。
Therefore, in JP-A-1-178597, a detergent composition containing N-acyl glutamic acid salt, N-anoralanine salt, and alkyl gliconide, which is hypoallergenic, has good foaming power, and has excellent foam quality, was developed. is proposed.

しかしこれも又、起泡力、洗浄力においては充分に満足
のいくものではなく、更にすすいだ後に皮膚にぬるつき
等の残留感が残ってしまうという欠点を有していた。
However, this also has the disadvantage that its foaming power and detergency are not fully satisfactory, and that it leaves a residual feeling such as sliminess on the skin after rinsing.

本発明者らは、N−アシルグルタミン酸やNアシルアラ
ニン塩とアルキルグリコシドの代わりに、N−アシルア
スパラギン酸塩とアルキルグリコシドを用いることによ
って、意外にも上記欠点が悉く政情され、特にぬるつき
感が大幅ムこ改善されることを見出し本発明を完成する
に至った。
By using N-acylaspartate and alkyl glycoside instead of N-acyl glutamic acid, N-acylalanine salt, and alkyl glycoside, the present inventors have surprisingly found that all the above-mentioned disadvantages are alleviated by the political situation, and in particular, the slimy feeling The present invention has been completed based on the discovery that this can significantly improve bulkiness.

〔発明が解決しようとする課題〕[Problem to be solved by the invention]

従って本発明の目的は、皮膚1毛髪に対して刺激が少な
く優れた起泡力、洗浄力を有し、かつすすいだ後洗浄剤
の残留感のない洗浄剤組成物を折供することにある。
Therefore, an object of the present invention is to provide a detergent composition that is less irritating to the skin and hair, has excellent foaming and detergent power, and does not leave a feeling of detergent residue after rinsing.

〔課題を解決するための手段〕[Means to solve the problem]

本発明は、一般式(A)で表されるN−アシルアスパラ
ギン酸塩と一般式(B)で表されるアルキルグリコンド
を含有する洗浄剤組成物である。
The present invention is a cleaning composition containing an N-acylaspartate represented by the general formula (A) and an alkyl glycode represented by the general formula (B).

一般式(A) (上記式中でR7は炭素数7〜21のアルキル基又はア
ルケニル基、M+ およびM!は水素又はNa’ 、に
’ 、NH=  もしくはアルカノールアミンから誘導
されるカチオンを表す、但しM、、M、が同時に水素で
あることはない、) 一般式(B) R2−〇 −(G)、。
General formula (A) (In the above formula, R7 is an alkyl group or alkenyl group having 7 to 21 carbon atoms, M+ and M! represent hydrogen or a cation derived from Na', Ni', NH= or alkanolamine, However, M and M are not hydrogen at the same time.) General formula (B) R2-〇-(G).

(式中R2は炭素数8〜18の直鎖又は分岐鎖のアルキ
ル基又はアルケニル基を、Gは炭素数5〜6を有する還
元糖に由来する残基を、nは1〜5の整数を表す。) 本発明に用いられる一般式(A)で表されるNアシルア
スパラギン酸塩としては、N〜ラウロイル−L−アスパ
ラギン酸ナトリウム、N−ヤシ油脂肪酸アシル−し−ア
スパラギン酸カリウム、N−ミリストイル−し−アスパ
ラギン酸ナトリウム7N−バルミトイル−L−アスパラ
ギン酸カリウムN−ステアロイル−L−アスパラギン酸
トリエタノールアミン等があるが、これらに限定される
ものではない。
(In the formula, R2 is a linear or branched alkyl group or alkenyl group having 8 to 18 carbon atoms, G is a residue derived from a reducing sugar having 5 to 6 carbon atoms, and n is an integer of 1 to 5. ) As the N-acylaspartate represented by the general formula (A) used in the present invention, N-sodium lauroyl-L-aspartate, N-potassium coconut oil fatty acyl-l-aspartate, N- Examples include, but are not limited to, sodium myristoyl-aspartate, 7N-valmitoyl-L-potassium aspartate, N-stearoyl-L-aspartate triethanolamine, and the like.

本発明で用いられる一般式(B)で表されるアルキルグ
リコシドのGの原料としては、単糖ではグルコース、ガ
ラクトース、フルクトース、マンノース、リキソース、
キシロース、アラビノース等が、2vM以上ではマルト
ース、イソマルトースキシロビオース、ラクトース、シ
ュクロース ラフィノース等が挙げられるが、これらに
限定されるものではない。これらのうち、好ましい原料
は、人手性及び低コストの点においてグルコース、フル
クトース、マルトース、シュクロースである。
As raw materials for G in the alkyl glycoside represented by the general formula (B) used in the present invention, examples of monosaccharides include glucose, galactose, fructose, mannose, lyxose,
Examples include xylose, arabinose, etc., and maltose, isomaltose, xylobiose, lactose, sucrose, raffinose, etc. at 2 vM or more, but are not limited to these. Among these, preferred raw materials are glucose, fructose, maltose, and sucrose in terms of ease of use and low cost.

そして、残基2個以上から構成されたアルキルグリコシ
ドの場合その糖鎖の結合様式は1−2.1.3.1−4
.1−6結合のいずれでも良い。また、Gの重合度nは
1〜5の整数であるが、それらの混合物(平均重合度1
.5のもの等)を用いることもできる。
In the case of an alkyl glycoside composed of two or more residues, the binding mode of the sugar chain is 1-2.1.3.1-4.
.. Any one of 1-6 bonds may be used. Further, the degree of polymerization n of G is an integer of 1 to 5, but a mixture thereof (average degree of polymerization 1
.. 5) can also be used.

一般式(A)  と(B)の総量は洗浄剤組成物全量中
大略3〜50重景%重量り好ましくは5〜30重量%で
ある。3重量%未溝の配合量では充分な起泡力、洗浄力
が得にくく、50%を超える配合量では安全性、安定性
の点で好ましくない。
The total amount of general formulas (A) and (B) is approximately 3 to 50% by weight, preferably 5 to 30% by weight, based on the total amount of the cleaning composition. A blending amount of 3% by weight without grooves makes it difficult to obtain sufficient foaming power and detergency, and a blending amount exceeding 50% is unfavorable in terms of safety and stability.

又、(A) /(B)の重量比は0.1〜10の範囲が
好ましい、この組成において0.1未満であると、起泡
力、洗浄力が充分に得られず10を超えると、皮膚及び
毛髪に対する温和な作用が期待で′ドなくなる。
In addition, the weight ratio of (A)/(B) is preferably in the range of 0.1 to 10; if it is less than 0.1 in this composition, sufficient foaming power and detergency cannot be obtained, and if it exceeds 10, I was overwhelmed with anticipation for its gentle effect on the skin and hair.

さらに本発明の洗浄剤組成物には、上記必須成分に加え
て洗浄剤に常用されている成分や添加剤を配合すること
も可能である。すなわち高級アルコール、シリコン油、
ラノリン誘導体、エステル油等の油分、ポリオキシエチ
レン硬化ヒマシ油等の非イオン界面活性剤3カチオン性
高分子〔ポリマーJR(ユニオンカーバイドコーポレー
ション社製)、ポリコートNH(ヘンケル社製)、マー
コート550 (メルク社製)、ガフカット755N(
GAF社製)等、殺菌剤、キレート剤、紫外線吸収剤2
動植物の天然エキス及びその誘導体、クエン酸等の有機
酸、塩化ナトリウム等の無機塩香料1色素等を、本発明
の効果を損なわない範囲で適宜配合することができる。
Furthermore, in addition to the above-mentioned essential components, the cleaning composition of the present invention can also contain components and additives commonly used in cleaning agents. Namely, higher alcohol, silicone oil,
Lanolin derivatives, oils such as ester oils, nonionic surfactants such as polyoxyethylene hydrogenated castor oil, etc.3 cationic polymers [Polymer JR (manufactured by Union Carbide Corporation), Polycoat NH (manufactured by Henkel), Marquat 550 (Merck ), Gaff Cut 755N (manufactured by
GAF), etc., disinfectants, chelating agents, ultraviolet absorbers2
Natural extracts of animals and plants and their derivatives, organic acids such as citric acid, inorganic salts such as sodium chloride, fragrances, pigments, etc. can be appropriately blended within the range that does not impair the effects of the present invention.

〔実施例〕〔Example〕

次に実施例によって本発明をさらに詳細に説明するが、
本発明はこれにより限定されるものではない。含有量は
重量%で表してあり、効果の測定は以下の試験法5評価
法によった。尚、蛋白質変性率を調べることによって、
皮膚刺激性試験に代えた。
Next, the present invention will be explained in more detail with reference to Examples.
The present invention is not limited thereby. The content is expressed in weight %, and the effectiveness was measured by the following Test Method 5 evaluation method. In addition, by examining the protein denaturation rate,
It was replaced with a skin irritation test.

(起泡力試験法) ロスマイルス法に準して起泡力を測定した。但し試料は
2%水溶液(CaCCL  50ppm人工硬水使用)
で、温度は40°Cである。
(Foaming power test method) Foaming power was measured according to the Ross Miles method. However, the sample is a 2% aqueous solution (CaCCL 50ppm artificial hard water used)
And the temperature is 40°C.

◎・・・泡立ちが極めて良好(起泡力250謳以上)○
・・・泡立ちが良好(起泡力210靴以上250■未満
) Δ・・・泡立ちが普通(起泡力170圃以上210画未
満 ×・・・泡立ちが不良(起泡力170mm未満)(洗浄
試験法) 5 cmX5 cmのウールモスリン布にラノリン7%
及びスダンI110.005%のクロロホルムを容液0
、4 m eを均一に塗布し乾燥させ、この汚染布を3
%の洗浄剤溶液40m1が入った約100mAのガラス
製シリンダー中に入れ、40°Cの恒温槽中で15分振
とうし、汚染布を流水中でよくすすぎ乾燥させ反射率を
調べ次式により洗浄率を求めた。
◎・・・Extremely good foaming (foaming power 250 or more)○
... Good foaming (foaming power 210 or more and less than 250) Δ... Normal foaming (foaming power 170 or more and less than 210 ×...poor foaming (foaming power less than 170 mm) Test method) 7% lanolin on a 5 cm x 5 cm wool muslin cloth.
and Sudan I 110.005% chloroform to a volume of 0.
, 4 m e was applied uniformly and dried, and the contaminated cloth was coated with 3 m e.
The contaminated cloth was placed in a glass cylinder of approximately 100 mA containing 40 ml of % cleaning solution and shaken for 15 minutes in a constant temperature bath at 40°C.The contaminated cloth was thoroughly rinsed under running water and dried, and the reflectance was determined using the following formula. The cleaning rate was determined.

又、評価の基準を次のように設定した。In addition, the evaluation criteria were set as follows.

◎・・・洗浄性優秀(洗浄率85%以上)○・・・洗浄
性良好(洗浄率70%以上85%未満)Δ・・・洗浄性
普通(洗浄率55%以上70%未満)×・・・洗浄性不
良(洗浄率55%未満)(蛋白質変性率試験法) 水系高速液体クロマトグラフィーを利用して卵白アルブ
ミンpH711衝溶液に試料濃度1%になるように試料
を加えた場合の、卵白アルブミン変性率を220nmの
吸収ピークを用いて測定した。
◎... Excellent cleaning performance (cleaning rate of 85% or more) ○... Good cleaning performance (cleaning rate of 70% or more and less than 85%) Δ... Fair cleaning performance (cleaning rate of 55% or more and less than 70%) ×・・・Poor cleaning performance (cleaning rate less than 55%) (Protein denaturation rate test method) When a sample is added to an egg albumin pH 711 buffer solution using aqueous high performance liquid chromatography at a sample concentration of 1%, the egg white The albumin modification rate was measured using the absorption peak at 220 nm.

Ho :卵白アルブミンの220nm吸収ピークの高さ H5:卵白アルブミン緩衝溶液に試料を加えた時の22
0nm吸収ピークの高さ 評価の基準を次のように設定した。
Ho: Height of the 220 nm absorption peak of ovalbumin H5: 22 when the sample is added to the ovalbumin buffer solution
The criteria for evaluating the height of the 0 nm absorption peak was set as follows.

◎・・・卵白アルブミン変性率30%未満O・・・卵白
アルブミン変性率30%以上60%未満Δ・・・卵白ア
ルブミン変性率60%以上80%未満×・・・卵白アル
ブミン変性率80%以上(ぬるつき感) 女子20人(パネル)が、本発明の洗浄剤を1週間連続
使用し、使用感を判定した。評価方法としては、各組成
物を浴用スポンジ上にとったものを用いてよく泡立て、
身体の洗浄を行う、その後温水を用いてすすぎ、そのす
すぎ後の身体の各部のぬるつき感を評価した。
◎... Ovalbumin denaturation rate less than 30% O... Ovalbumin denaturation rate 30% or more and less than 60% Δ... Ovalbumin denaturation rate 60% or more and less than 80% ×... Ovalbumin denaturation rate 80% or more (Slimy feeling) Twenty women (panel) continuously used the cleaning agent of the present invention for one week and evaluated the feeling of use. As an evaluation method, each composition was placed on a bath sponge and lathered thoroughly.
The body was washed, then rinsed with warm water, and the slimy feeling of each part of the body after rinsing was evaluated.

◎・・・ぬるつき感がない O・・・ぬるつき感がほとんどない Δ・・・ぬるつき感がややある ×・・・ぬるつき感が大きい 実施例1〜5.比較例1〜7 第1表に示す組成の洗浄剤を通常の方法で調製し、各必
須成分の効果を調べ第1表にその効果を示した。
◎... No slimy feeling O... Almost no slimy feeling Δ... Slightly slimy feeling ×... Large slimy feeling Examples 1 to 5. Comparative Examples 1 to 7 Cleaning agents having the compositions shown in Table 1 were prepared in a conventional manner, and the effects of each essential component were examined and the effects are shown in Table 1.

第1表から明らかなように、実施例1〜5に示す本発明
の成分を用いた洗浄剤はいずれも優れた性能を示してい
た。一方、アスパラギン酸以外のアミノ酸から合成され
るN−アシルアミノ酸塩を用いた比較例1.2は、皮膚
刺激はないものの、ぬるつき感が残り、起泡力、洗浄性
は実施例よりは劣る。N−アシルアスパラギン酸か又は
アルキルグリコシドのいずれかを欠いた比較例3.4は
、起泡力、洗浄性に劣り、ぬるつきもあった。
As is clear from Table 1, all of the cleaning agents using the components of the present invention shown in Examples 1 to 5 showed excellent performance. On the other hand, Comparative Example 1.2 using an N-acyl amino acid salt synthesized from an amino acid other than aspartic acid did not cause skin irritation, but a slimy feeling remained, and the foaming power and cleansing performance were inferior to the examples. . Comparative Example 3.4 lacking either N-acylaspartic acid or alkyl glycoside had poor foaming power and detergency, and was also slimy.

実施例6 次の組成よりなる頭髪用シャンプーを調製し前記の方法
にて評価した。
Example 6 A shampoo for hair having the following composition was prepared and evaluated using the method described above.

配合組成           (重量%)アルキルグ
リコンド (C1□〜+  −O(G)+〜Z)       7
.ON−ラウロイル−L−アスパラギン酸 トリエタノールアミン         17.0加水
分解シルク             0.2ジプロピ
レングリコール        3.0色素、香料  
            適量精製水        
        残余実施例7 次の組成よりなるボディーシャンプーを調製して前記の
方法にて評価した。
Blend composition (wt%) Alkyl glycond (C1□~+ -O(G)+~Z) 7
.. ON-lauroyl-L-aspartate triethanolamine 17.0 Hydrolyzed silk 0.2 Dipropylene glycol 3.0 Pigment, fragrance
Appropriate amount of purified water
Remaining Example 7 A body shampoo having the following composition was prepared and evaluated using the method described above.

配合組成           (重量%)アルキルグ
リコシド CC+t〜−h  O(G)+〜z )       
2. ON−ヤシ油脂肪酸アシル−し アスパラギン酸カリウム       15.0ヤシ油
脂肪酸エチルエステル 硫酸ナトリウム             2.0ジス
テアリン酸エチレングリコール   0.8濃グリセリ
ン              2.0色素3香料  
            適量精製水        
        残余実施例6.及び7の頭髪用シャン
プー及びボディーシャンプーは起泡性、洗浄性、安全性
、使用時の感触において満足のいくものであった。
Blend composition (wt%) alkyl glycoside CC+t~-h O(G)+~z)
2. ON-coconut oil fatty acid acyl-potassium aspartate 15.0 coconut oil fatty acid ethyl ester sodium sulfate 2.0 ethylene glycol distearate 0.8 concentrated glycerin 2.0 color 3 fragrance
Appropriate amount of purified water
Remaining Example 6. The hair shampoo and body shampoo of Nos. 7 and 7 were satisfactory in terms of foaming properties, cleansing properties, safety, and feel during use.

〔発明の効果〕〔Effect of the invention〕

本発明は、皮膚に対する刺激が少なく起泡性。 The present invention is less irritating to the skin and has foaming properties.

洗浄性に優れている。更に、N−アシルアスパラギン酸
塩のかわりに、N−アシルグルタミン酸塩やN−アシル
−β−アラニン塩等を用いた時に比べて、使用後のぬる
つき感が大幅に改善されており、さっばりとした感触が
得られる洗浄剤組成物であることは明らかである。
Excellent cleaning properties. Furthermore, compared to when N-acyl glutamate or N-acyl-β-alanine salt was used instead of N-acylaspartate, the slimy feeling after use was significantly improved and the product felt light and refreshing. It is clear that this is a cleaning composition that provides a soft feel.

Claims (1)

【特許請求の範囲】  下記の一般式(A)で表されるN−アシルアスパラギ
ン酸塩と下記一般式(B)で表されるアルキルグリコシ
ドを含有する洗浄剤組成物 一般式(A) ▲数式、化学式、表等があります▼ (上記式中でR_1は炭素数7〜21のアルキル基又は
アルケニル基、M_1およびM_2は水素又はNa^+
、K^+、NH_4^+もしくはアルカノールアミンか
ら誘導されるカチオンを表す。但しM_1、M_2が同
時に水素であることはない。) 一般式(B) R_2−O−(G)_n (式中R_2は炭素数8〜18の直鎖又は分岐鎖のアル
キル基又はアルケニル基を、Gは炭素数5〜6を有する
還元糖に由来する残基を、nは1〜5の整数を表す。)
[Scope of Claims] A cleaning composition containing an N-acylaspartate represented by the following general formula (A) and an alkyl glycoside represented by the following general formula (B) General formula (A) ▲Mathematical formula , chemical formulas, tables, etc. ▼ (In the above formula, R_1 is an alkyl group or alkenyl group having 7 to 21 carbon atoms, M_1 and M_2 are hydrogen or Na^+
, K^+, NH_4^+ or a cation derived from an alkanolamine. However, M_1 and M_2 are never hydrogen at the same time. ) General formula (B) R_2-O-(G)_n (In the formula, R_2 is a linear or branched alkyl group or alkenyl group having 8 to 18 carbon atoms, and G is a reducing sugar having 5 to 6 carbon atoms.) n represents an integer from 1 to 5.)
JP23614090A 1990-09-05 1990-09-05 Detergent composition Expired - Fee Related JP2744516B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP23614090A JP2744516B2 (en) 1990-09-05 1990-09-05 Detergent composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP23614090A JP2744516B2 (en) 1990-09-05 1990-09-05 Detergent composition

Publications (2)

Publication Number Publication Date
JPH04114100A true JPH04114100A (en) 1992-04-15
JP2744516B2 JP2744516B2 (en) 1998-04-28

Family

ID=16996354

Family Applications (1)

Application Number Title Priority Date Filing Date
JP23614090A Expired - Fee Related JP2744516B2 (en) 1990-09-05 1990-09-05 Detergent composition

Country Status (1)

Country Link
JP (1) JP2744516B2 (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN108570375A (en) * 2017-09-22 2018-09-25 无锡市科姆斯化工科技有限公司 A kind of environment protection clean liquid detergent
WO2018234648A1 (en) 2017-06-22 2018-12-27 Societe D'exploitation De Produits Pour Les Industries Chimiques Seppic Novel surfactant mixture, novel composition comprising same and use thereof in cosmetics

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2018234648A1 (en) 2017-06-22 2018-12-27 Societe D'exploitation De Produits Pour Les Industries Chimiques Seppic Novel surfactant mixture, novel composition comprising same and use thereof in cosmetics
FR3068043A1 (en) * 2017-06-22 2018-12-28 Societe D'exploitation De Produits Pour Les Industries Chimiques Seppic NOVEL SURFACE MIXTURE, NOVEL COMPOSITION COMPRISING THE SAME AND ITS USE IN COSMETICS
CN110996895A (en) * 2017-06-22 2020-04-10 化工产品开发公司Seppic Novel surfactant mixtures, novel compositions comprising them and their use in cosmetics
CN108570375A (en) * 2017-09-22 2018-09-25 无锡市科姆斯化工科技有限公司 A kind of environment protection clean liquid detergent

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