JPH06128587A - Detergent composition - Google Patents
Detergent compositionInfo
- Publication number
- JPH06128587A JPH06128587A JP4278682A JP27868292A JPH06128587A JP H06128587 A JPH06128587 A JP H06128587A JP 4278682 A JP4278682 A JP 4278682A JP 27868292 A JP27868292 A JP 27868292A JP H06128587 A JPH06128587 A JP H06128587A
- Authority
- JP
- Japan
- Prior art keywords
- shampoo
- detergent
- compsn
- acid
- group
- 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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Classifications
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/38—Products with no well-defined composition, e.g. natural products
- C11D3/382—Vegetable products, e.g. soya meal, wood flour, sawdust
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/02—Anionic compounds
- C11D1/04—Carboxylic acids or salts thereof
- C11D1/10—Amino carboxylic acids; Imino carboxylic acids; Fatty acid condensates thereof
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Wood Science & Technology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Chemistry (AREA)
- Detergent Compositions (AREA)
- Cosmetics (AREA)
Abstract
Description
【0001】[0001]
【産業上の利用分野】本発明は、皮膚に対する刺激が著
しく低い洗浄剤組成物に関するものである。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a cleansing composition having extremely low skin irritation.
【0002】[0002]
【従来の技術】従来、洗浄剤には起泡性や洗浄力の良さ
からスルホン酸基もしくは、硫酸基を有するアニオン界
面活性剤、例えば、オレフィンスルホン酸塩、アルキル
硫酸塩、アルキルエーテル硫酸塩などが用いられてき
た。2. Description of the Related Art Conventionally, anionic surfactants having a sulfonic acid group or a sulfuric acid group, such as olefin sulfonates, alkyl sulfates, alkyl ether sulfates, etc., have been used as detergents because of their good foamability and detergency Has been used.
【0003】[0003]
【発明が解決しようとする課題】しかし、これらの界面
活性剤を主剤とする洗浄剤を連用すると手荒れなどを起
こすことがあり、家庭における食器洗いや業としての食
器洗い、洗髪等に携わる人々から手荒れなどを起こさな
い洗浄剤が求められていた。このような手荒れなどは上
記界面活性剤の蛋白変性力の強さや皮膚一次刺激によっ
て引き起こされると考えられている。このため、蛋白変
性力のより低い界面活性剤を用いたり、皮膚一次刺激性
が低い成分を用いた洗浄剤が提案されてきたが、まだ十
分満足できるものはなかった。However, continuous use of detergents containing these surfactants as the main ingredient may cause hand roughening, etc., so that people involved in dishwashing at home, dishwashing as work, and hair washing etc. may get rough hands. There has been a demand for a cleaning agent that does not cause It is considered that such rough hands are caused by the strong protein denaturing power of the above-mentioned surfactant and primary skin irritation. For this reason, detergents using a surfactant having a lower protein denaturing power or a component having a low primary skin irritation have been proposed, but none have been sufficiently satisfied.
【0004】[0004]
【課題を解決する手段および作用】発明者らは上記課題
を解決することを目的として鋭意研究を続けてきたが、
N−アシルアミノ酸またはその塩を主たる成分として、
これにグリチルリチン酸、グリチルリチン酸の塩または
マロニエエキスのうちの少なくとも一種類を配合する
と、蛋白変性力及び皮膚一次刺激性が低く、手荒れ等を
起こすさず、しかも洗浄性や起泡性に優れた洗浄剤が得
られることを見いだし、本発明を完成するに至った。[Means and Actions for Solving the Problems] The inventors have conducted earnest research for the purpose of solving the above problems.
With N-acyl amino acid or its salt as the main component,
When at least one of glycyrrhizic acid, a salt of glycyrrhizic acid, and horse chestnut extract is added to this, the protein denaturing power and primary skin irritation are low, it does not cause rough hands and the like, and is excellent in cleanability and foamability. The inventors have found that a cleaning agent can be obtained, and completed the present invention.
【0005】すなわち、本発明の洗浄剤組成物は、下記
(a)群から選択される単数または複数の成分と、下記
(b)群および(c)群の少なくとも一方から選択され
る単数または複数の成分とを含有することを特徴とす
る。 (a)N−アシルアミノ酸およびその塩。That is, the cleaning composition of the present invention comprises one or more components selected from the following (a) group and one or more components selected from at least one of the following (b) group and (c) group. And a component of. (A) N-acyl amino acids and salts thereof.
【0006】(b)グリチルリチン酸およびその塩。 (c)マロニエエキス。 以下、本発明についてさらに詳しく述べる。本発明に用
いられる(a)群成分としてのN−アシルアミノ酸およ
びその塩は下記(1)式に示す一般式で表される。(B) Glycyrrhizic acid and salts thereof. (C) Horse chestnut extract. Hereinafter, the present invention will be described in more detail. The N-acyl amino acid and its salt as the component (a) used in the present invention are represented by the following general formula (1).
【0007】[0007]
【化1】 [Chemical 1]
【0008】ただし、(1)式中、R1は炭素数9〜1
8の直鎖のアルキル基または分岐のアルキレン基、R2
はHまたは炭素数1〜4のアルキル基、R3は炭素数1
〜2の直鎖もしくは分岐のアルキレン基または下記
(2)式に示す一般式で表される基のものが通常使用さ
れる。However, in the formula (1), R 1 has 9 to 1 carbon atoms.
8, a straight-chain alkyl group or a branched alkylene group, R 2
Is H or an alkyl group having 1 to 4 carbon atoms, R 3 is 1 carbon atom
The linear or branched alkylene group represented by the formula (1) to (2) or the group represented by the general formula shown in the following formula (2) is usually used.
【0009】[0009]
【化2】 [Chemical 2]
【0010】この(a)群のN−アシルアミノ酸および
その塩の例としては、N−アシル−L−グルタミン酸
類、N−アシルサルコシン類およびN−アシル−N−メ
チル−β−アラニン類がある。これらをさらに詳しく例
示すると、N−アシル−L−グルタミン酸類としては、
N−ラウロイル−L−グルタミン酸、N−ステアロイル
−L−グルタミン酸、N−パルミトイル−L−グルタミ
ン酸、N−ミリストイル−L−グルタミン酸、N−オレ
オイル−L−グルタミン酸、N−ヤシ油脂肪酸アシル−
L−グルタミン酸、N−硬化牛脂脂肪酸アシル−L−グ
ルタミン酸、N−ヤシ油脂肪酸・硬化牛脂脂肪酸アシル
−L−グルタミン酸、N−アシル(12〜18)−L−
グルタミン酸およびこれらのナトリウム、カリウム、モ
ノエタノールアミン、ジエタノールアミン、トリエタノ
ールアミン塩などが挙げられる。Examples of N-acyl amino acids and salts thereof of this group (a) include N-acyl-L-glutamic acids, N-acyl sarcosines and N-acyl-N-methyl-β-alanines. . To further exemplify these, as N-acyl-L-glutamic acids,
N-lauroyl-L-glutamic acid, N-stearoyl-L-glutamic acid, N-palmitoyl-L-glutamic acid, N-myristoyl-L-glutamic acid, N-oleoyl-L-glutamic acid, N-coconut fatty acid acyl-
L-glutamic acid, N-hardened beef tallow fatty acid acyl-L-glutamic acid, N-coconut oil fatty acid / hardened beef tallow fatty acid acyl-L-glutamic acid, N-acyl (12-18) -L-
Examples thereof include glutamic acid and sodium, potassium, monoethanolamine, diethanolamine, triethanolamine salts thereof and the like.
【0011】また、N−アシルサルコシン類としては、
オレオイルサルコシン、ラウロイルサルコシン、ミリス
トイルサルコシン、パルミトイルサルコシン、ステアロ
イルサルコシン、ベヘロイルサルコシン、ヤシ油脂肪酸
サルコシン、ヤシ油脂肪酸メチルタウリン、N−ミリス
トイルメチルタウリン、N−パルミトイルメチルタウリ
ン、N−ステアロイルメチルタウリン、N−ベヘロイル
メチルタウリンおよびこれらのナトリウム、カリウム、
アンモニウム、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塩などが挙げられる。Further, as N-acyl sarcosines,
Oleoyl sarcosine, lauroyl sarcosine, myristoyl sarcosine, palmitoyl sarcosine, stearoyl sarcosine, beheroyl sarcosine, coconut oil fatty acid sarcosine, coconut oil fatty acid methyl taurine, N-myristoyl methyl taurine, N-palmitoyl methyl taurine, N-stearoyl methyl taurine, N-beheroylmethyl taurine and their sodium, potassium,
Examples thereof include ammonium, monoethanolamine, diethanolamine and triethanolamine salts.
【0012】さらに、N−アシル−N−メチル−β−ア
ラニン類としては、N−ミリストイル−N−メチル−β
−アラニン、N−ラウロイル−N−メチル−β−アラニ
ン、N−ヤシ油脂肪酸−N−メチル−β−アラニンおよ
びこれらのナトリウム、カリウム、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塩など
が挙げられる。Further, as N-acyl-N-methyl-β-alanines, N-myristoyl-N-methyl-β is available.
-Alanine, N-lauroyl-N-methyl-β-alanine, N-coconut oil fatty acid-N-methyl-β-alanine and their sodium, potassium, monoethanolamine, diethanolamine, triethanolamine salts and the like.
【0013】これらの中でも、泡のきめ細かさからN−
アシル−L−グルタミン酸類が特に好ましい。また、そ
の配合量は泡立ちの点から3重量%以上が好ましい。本
発明における(b)群成分としてのグリチルリチン酸お
よびその塩は、漢方の重要生薬として知られる甘草(カ
ンゾウ)の薬効成分であり、抗炎症作用、抗アレルギー
作用、解毒作用、創傷治癒作用が報告されている。その
塩としては、三ナトリウム、ジカリウム、アンモニウム
塩が挙げられる。この中でも、水への溶解性から、グリ
チルリチン酸ジカリウムを用いるのが好ましい。(b)
群成分の配合量が0.01重量%未満になると効果が低
くなり始め、1.0重量%を越えるとN−アシルアミノ
酸を含む溶液への溶解性が低くなる。このため(b)群
成分の配合量は、0.01重量%〜1.0重量%が好ま
しい。Among these, N- because of the fineness of bubbles.
Acyl-L-glutamic acids are particularly preferred. Further, the blending amount thereof is preferably 3% by weight or more from the viewpoint of foaming. Glycyrrhizic acid and a salt thereof as the (b) group component in the present invention are the medicinal components of licorice (liquorice) known as an important herbal medicine of Kampo, and have reported anti-inflammatory action, anti-allergic action, detoxification action, and wound healing action. Has been done. Examples of the salt include trisodium, dipotassium and ammonium salts. Among these, it is preferable to use dipotassium glycyrrhizinate because of its solubility in water. (B)
If the compounding amount of the group component is less than 0.01% by weight, the effect starts to decrease, and if it exceeds 1.0% by weight, the solubility in the solution containing the N-acylamino acid becomes low. Therefore, the blending amount of the component (b) is preferably 0.01% by weight to 1.0% by weight.
【0014】(c)群成分のマロニエエキスはセイヨウ
トチノキからの抽出物であり、その中に含まれるエスシ
ンにより、抗炎症作用、抗浮しゅ作用が認められている
物質である。(c)群成分の配合量が0.001重量%
未満になると効果が低くなり始め、1.0重量%を越え
るとN−アシルアミノ酸を含む溶液への溶解性が低くな
る。したがって、(c)群成分の配合量は、固形分とし
て0.001重量%〜1.0重量%が好ましい。The horse chestnut extract, which is a component of group (c), is an extract from horse chestnut and is a substance for which escin contained therein has an anti-inflammatory action and an anti-edema action. (C) Group component content is 0.001% by weight
If it is less than 1.0%, the effect tends to be low, and if it exceeds 1.0% by weight, the solubility in a solution containing an N-acylamino acid becomes low. Therefore, the blending amount of the group (c) component is preferably 0.001% by weight to 1.0% by weight as a solid content.
【0015】上記(a)群から選択される成分と、
(b)群または(c)群成分の一方を配合したのみで
も、手荒れ等を起こさず、しかも洗浄性や起泡性に優れ
た洗浄剤組成物が得られるが、(b)群および(c)群
の双方から選択される成分を配合すると一層良好であ
る。A component selected from the group (a),
Even if only one of the components of the (b) group or the (c) group is blended, a detergent composition which does not cause rough hands and has excellent detergency and foamability can be obtained. It is even better to incorporate ingredients selected from both groups.
【0016】本発明の洗浄剤組成物には、洗浄剤に一般
に用いられる成分を任意成分として配合することが可能
である。例えば油分、ノニオン界面活性剤、両性界面活
性剤、高級アルコール、保湿剤、増粘剤、コンディショ
ニング剤、金属封鎖剤、pH調整剤、紫外線吸収剤、殺
菌剤、防腐剤、色素、香料等である。The detergent composition of the present invention may contain, as an optional component, components generally used in detergents. For example, oils, nonionic surfactants, amphoteric surfactants, higher alcohols, humectants, thickeners, conditioning agents, sequestering agents, pH adjusters, UV absorbers, bactericides, preservatives, dyes, fragrances, etc. .
【0017】本発明の洗浄剤組成物は、例えばシャンプ
ー、ボディシャンプー、手洗い洗浄剤、洗顔料、台所用
洗浄剤、衣類用洗浄剤、ペット用シャンプー、カーペッ
ト用シャンプー、住居用シャンプーなどとして使用でき
る。The detergent composition of the present invention can be used, for example, as a shampoo, a body shampoo, a hand-washing detergent, a facial cleanser, a kitchen detergent, a laundry detergent, a pet shampoo, a carpet shampoo, a residential shampoo and the like. .
【0018】[0018]
【実施例】下記の表1に示す配合比でシャンプーとして
調製した実施例1〜5および表2に示す配合比で調製し
た比較例1〜4の洗浄剤組成物に下記(1)〜(4)の
評価試験を実施し、その結果を表3に示した。EXAMPLES Examples 1 to 5 prepared as shampoos with the compounding ratios shown in Table 1 below, and Comparative Examples 1 to 4 prepared with the compounding ratios shown in Table 2 have the following (1) to (4 ) Was carried out, and the results are shown in Table 3.
【0019】[0019]
【表1】 [Table 1]
【0020】[0020]
【表2】 [Table 2]
【0021】[評価試験] (1)蛋白変性率測定 高速液体クロマトグラフィーを用い、卵白アルブミンp
H7緩衝液に試料濃度0.8%になるよう試料を添加し
た際の卵白アルブミンの220nmの吸収ピークを測定
し蛋白変性率とした。[Evaluation test] (1) Measurement of protein denaturation rate Using ovalbumin p using high performance liquid chromatography.
The 220 nm absorption peak of ovalbumin when the sample was added to the H7 buffer at a sample concentration of 0.8% was determined as the protein denaturation rate.
【0022】[0022]
【数1】 [Equation 1]
【0023】設定した判定基準は以下のとおりである。 ◎:蛋白変性率20%未満 ○:蛋白変性率20%以上40%未満 △:蛋白変性率40%以上70%未満 ×:蛋白変性率70%以上 (2)手荒れ試験 20名のパネラーにより、左右どちらかの手を試料濃度
5%、温度40℃の水溶液に、他方の手を40℃の温水
に浸す操作を1日3回、3日間連続で行い左右の手荒れ
状態を肉眼観察した。The judgment criteria set are as follows. ⊚: Protein denaturation rate of less than 20% ◯: Protein denaturation rate of 20% or more and less than 40% Δ: Protein denaturation rate of 40% or more and less than 70% ×: Protein denaturation rate of 70% or more (2) Hand roughness test Left and right by 20 panelists An operation of immersing one hand in an aqueous solution having a sample concentration of 5% and a temperature of 40 ° C. and the other hand in hot water of 40 ° C. three times a day for three consecutive days was performed, and the rough condition of the left and right hands was visually observed.
【0024】設定した判定基準は以下のとおりである。 ◎:20人中 0〜2人 試料側に手荒れが認めら
れた。 ○:20人中 3〜6人 試料側に手荒れが認めら
れた。 △:20人中 7〜14人 試料側に手荒れが認めら
れた。The set judgment criteria are as follows. ⊚: 0 to 2 out of 20 people Rough hands were observed on the sample side. ◯: 3 to 6 out of 20 people Rough hands were observed on the sample side. Δ: 7 to 14 out of 20 samples Roughness was recognized on the sample side.
【0025】×:20人中 15〜20人 試料側に手
荒れが認められた。 (3)皮膚一次刺激性試験 20名のパネラーにより、試料濃度1%の水溶液0.2
mlをしみ込ませたパッチテスト用絆創膏を24時間閉
鎖貼付し、貼付除去後に肉眼で刺激性を判定した。X: 15 to 20 out of 20 Rough hands were observed on the sample side. (3) Primary skin irritation test An aqueous solution with a sample concentration of 1% 0.2 by 20 panelists
A patch test adhesive bandage impregnated with ml was adhered to the skin for 24 hours, and the irritation was visually determined after the adhesive was removed.
【0026】設定した判定基準は以下のとおりである。 ◎:はっきりした紅斑を示した者 0〜2名 ○:はっきりした紅斑を示した者 3〜6名 △:はっきりした紅斑を示した者 7〜14名 ×:はっきりした紅斑を示した者 15〜20名 (4)使用感 10名のパネラーにより、泡立ちおよびきめの細かさを
5点法で評価し、その合計点で判定した。The judgment criteria set are as follows. ◎: 0 to 2 people who showed clear erythema ○: 3 to 6 people who showed clear erythema △: 7 to 14 people who showed clear erythema ×: People who showed clear erythema 15 to 20 people (4) Feel of use 10 panelists evaluated the fineness of foaming and texture by a 5-point method, and judged by the total score.
【0027】設定した判定基準は以下のとおりである。 ◎:合計点、40点以上 ○:合計点、30点以上40点未満 △:合計点、20点以上30点未満 ×:合計点、20点未満The judgment criteria set are as follows. ◎: Total points, 40 points or more ○: Total points, 30 points or more and less than 40 points △: Total points, 20 points or more and less than 30 points ×: Total points, less than 20 points
【0028】[0028]
【表3】 [Table 3]
【0029】表3から明らかなように本発明の洗浄剤組
成物(実施例1〜5)によるシャンプーは刺激性は低く
手荒れを起こしにくい。しかも使用感に優れている。ま
た、別途実施した実験では、実施例1〜5の洗浄剤組成
物によるシャンプーは洗浄性および起泡性に優れてい
た。 [実施例6]次の組成で、洗浄剤組成物を食器洗浄剤と
して調整した。As is apparent from Table 3, the shampoos prepared from the detergent compositions of the present invention (Examples 1 to 5) have low irritation and are less likely to cause rough hands. Moreover, it has excellent usability. In an experiment conducted separately, the shampoos prepared with the detergent compositions of Examples 1 to 5 were excellent in detergency and foamability. [Example 6] A detergent composition having the following composition was prepared as a dishwashing agent.
【0030】 配合比(重量%) (a)N−ヤシ油脂肪酸アシル−L−グルタミン酸ナトリウム 6 (b)グリチルリチン酸ジカリウム 0.2 (c)マロニエエキス (固形分3%) 3 ラウリン酸ジエタノールアミド 3 ポリオキシエチレンラウリルエーテル 5 ラウリルジメチルアミンオキシド(30%) 2 メチルパラベン 0.1 香料 0.1 水 残余 この洗浄剤組成物は実施例1〜5と同様に、刺激性、手
荒れの発生および使用感において優れた効果が認めら
れ、洗浄性および起泡性に優れていた。 [実施例7]次の組成で、洗浄剤組成物を洗顔料として
調整した。Mixing ratio (% by weight) (a) N-coconut oil fatty acid acyl-L-glutamate sodium 6 (b) Dipotassium glycyrrhizinate 0.2 (c) Horse chestnut extract (solid content 3%) 3 Lauric acid diethanolamide 3 Polyoxyethylene lauryl ether 5 Lauryl dimethylamine oxide (30%) 2 Methylparaben 0.1 Perfume 0.1 Water Residual This detergent composition was the same as in Examples 1 to 5 in terms of irritation, occurrence of rough skin and feeling of use. An excellent effect was recognized, and it was excellent in cleaning property and foaming property. [Example 7] A detergent composition having the following composition was prepared as a face wash.
【0031】 配合比(重量%) (a)N−ミリストイル−L−グルタミン酸ナトリウム 5 (b)グリチルリチン酸ジカリウム 0.2 (c)マロニエエキス末 0.2 ヤシ油脂肪酸ジエタノールアミド 5 カルボキシビニルポリマー 0.6 トリエタノールアミン 0.8 グリセリン 1 メチルパラベン 0.1 香料 0.1 水 残余 この洗浄剤組成物は実施例1〜5と同様に、刺激性、手
荒れの発生および使用感において優れた効果が認めら
れ、洗浄性および起泡性に優れていた。Mixing ratio (% by weight) (a) N-myristoyl-L-glutamate 5 (b) Dipotassium glycyrrhizinate 0.2 (c) Horse chestnut extract powder 0.2 Palm oil fatty acid diethanolamide 5 Carboxyvinyl polymer 0. 6 Triethanolamine 0.8 Glycerin 1 Methylparaben 0.1 Perfume 0.1 Water Residual This detergent composition was found to have excellent effects on irritation, occurrence of rough skin and feeling of use, as in Examples 1 to 5. It was excellent in detergency and foamability.
【0032】[0032]
【発明の効果】以上のように、本発明の洗浄剤組成物
は、手荒れ等を起こしにくく、しかも洗浄性や起泡性に
優れている。Industrial Applicability As described above, the detergent composition of the present invention is less likely to cause rough hands and is excellent in detergency and foamability.
Claims (1)
複数の成分と、下記(b)群および(c)群の少なくと
も一方から選択される単数または複数の成分とを含有す
ることを特徴とする洗浄剤組成物。 (a)N−アシルアミノ酸およびその塩。 (b)グリチルリチン酸およびその塩。 (c)マロニエエキス。1. A composition comprising one or more components selected from the following group (a) and one or more components selected from at least one of the following groups (b) and (c): And a cleaning composition. (A) N-acyl amino acids and salts thereof. (B) Glycyrrhizic acid and salts thereof. (C) Horse chestnut extract.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP4278682A JPH06128587A (en) | 1992-10-16 | 1992-10-16 | Detergent composition |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP4278682A JPH06128587A (en) | 1992-10-16 | 1992-10-16 | Detergent composition |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH06128587A true JPH06128587A (en) | 1994-05-10 |
Family
ID=17600707
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP4278682A Pending JPH06128587A (en) | 1992-10-16 | 1992-10-16 | Detergent composition |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH06128587A (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2007112914A (en) * | 2005-10-21 | 2007-05-10 | Taiyo Kagaku Co Ltd | Liquid detergent composition |
JP2009046399A (en) * | 2007-08-14 | 2009-03-05 | Kon Junichi | Dog body care system and dog body cleanser |
JP2010090043A (en) * | 2008-10-06 | 2010-04-22 | Milbon Co Ltd | Shampoo |
CN113174300A (en) * | 2021-04-14 | 2021-07-27 | 大连工业大学 | Grease-based acyl amino acid salt infant laundry detergent and preparation method thereof |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH03111500A (en) * | 1989-09-27 | 1991-05-13 | Kawaken Fine Chem Co Ltd | Gel detergent |
JPH05117695A (en) * | 1991-03-14 | 1993-05-14 | Manabisu:Kk | Cleaning composition for nursing bottle and tableware |
JPH05140590A (en) * | 1991-08-09 | 1993-06-08 | Manabisu:Kk | Cleanser composition having color-developing and decoloring function |
-
1992
- 1992-10-16 JP JP4278682A patent/JPH06128587A/en active Pending
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH03111500A (en) * | 1989-09-27 | 1991-05-13 | Kawaken Fine Chem Co Ltd | Gel detergent |
JPH05117695A (en) * | 1991-03-14 | 1993-05-14 | Manabisu:Kk | Cleaning composition for nursing bottle and tableware |
JPH05140590A (en) * | 1991-08-09 | 1993-06-08 | Manabisu:Kk | Cleanser composition having color-developing and decoloring function |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2007112914A (en) * | 2005-10-21 | 2007-05-10 | Taiyo Kagaku Co Ltd | Liquid detergent composition |
JP2009046399A (en) * | 2007-08-14 | 2009-03-05 | Kon Junichi | Dog body care system and dog body cleanser |
JP2010090043A (en) * | 2008-10-06 | 2010-04-22 | Milbon Co Ltd | Shampoo |
CN113174300A (en) * | 2021-04-14 | 2021-07-27 | 大连工业大学 | Grease-based acyl amino acid salt infant laundry detergent and preparation method thereof |
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