JPH05156297A - Detergent composition - Google Patents

Detergent composition

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Publication number
JPH05156297A
JPH05156297A JP32069691A JP32069691A JPH05156297A JP H05156297 A JPH05156297 A JP H05156297A JP 32069691 A JP32069691 A JP 32069691A JP 32069691 A JP32069691 A JP 32069691A JP H05156297 A JPH05156297 A JP H05156297A
Authority
JP
Japan
Prior art keywords
detergent composition
acid salt
component
potassium
alkanolammonium
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
JP32069691A
Other languages
Japanese (ja)
Other versions
JP3087401B2 (en
Inventor
Toshio Nozaki
利雄 野崎
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.)
Kao Corp
Original Assignee
Kao Corp
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 Kao Corp filed Critical Kao Corp
Priority to JP32069691A priority Critical patent/JP3087401B2/en
Publication of JPH05156297A publication Critical patent/JPH05156297A/en
Application granted granted Critical
Publication of JP3087401B2 publication Critical patent/JP3087401B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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  • Detergent Compositions (AREA)
  • Cosmetics (AREA)

Abstract

PURPOSE:To provide the subject composition containing a secondary amide-type N-acylamino acid salt and an antiphlogistic, excellent in detergency, low in irritation, showing an excellent anti-inflammatory effect and excellent in its durability. CONSTITUTION:The objective composition contains (A) a compound of the formula (R<1>CO is a 10-16C straight chain acyl; n is 1 or 2; M is sodium, potassium or alkanolammonium in the case of n=1 and potassium or an alkanolammonium in the case of n=2), (B) an antiphlogistic such as allantoin, ichthammol or quaiazulene and (C) a higher fatty acid salt, e.g. in the case of a liquid detergent in an amount of 5 to 50wt.% component (A) and 0.01 to 5.0 wt.% (preferably 0.05 to 2 wt.%) component (B) and preferably in a weight ratio of [the component (C)/the component (A)]=[(1/20) to (1/2)] [preferably (1/10) to (1/3)].

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明は洗浄剤組成物に関し、さ
らに詳細には皮膚及び毛髪に対して低刺激で、洗浄力が
高く、使用感が良好でかつ消炎作用及びその持続性に優
れた洗浄剤組成物に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a detergent composition, and more specifically, it has low irritation to the skin and hair, a high detergency, a good feeling of use, and an excellent anti-inflammatory action and its durability. Detergent composition.

【0002】[0002]

【従来の技術】従来、消炎性洗浄剤としては、種々の界
面活性剤に洗浄剤を配合した薬用洗浄料等が用いられて
いる。しかしながら、洗浄剤に消炎剤を配合した場合、
洗浄により消炎剤自体も皮膚又は毛髪から洗い流されて
しまって、充分に残存せず、洗浄後に皮膚上に発生する
炎症に対してはほとんどその効果を発揮し得ないという
問題があった。そこで一時的にその効果を高めるために
消炎剤の配合量を増やすということも考えられるが、効
果の発現に充分なだけの量を配合するのはかなり困難で
ある上、多量に配合しても、その効果は一時的には高ま
るが、持続性が悪く、不充分であった。
2. Description of the Related Art Conventionally, as a flame-retardant detergent, a medicinal detergent containing various surfactants mixed with a detergent has been used. However, when an anti-inflammatory agent is added to the cleaning agent,
There is a problem that the anti-inflammatory agent itself is washed away from the skin or hair by washing and does not remain sufficiently, and it is hardly possible to exert its effect on the inflammation generated on the skin after washing. Therefore, it is possible to temporarily increase the amount of the anti-inflammatory agent to increase the effect, but it is quite difficult to add an amount sufficient to exhibit the effect, and even if a large amount is added. , The effect was temporarily increased, but the sustainability was poor and it was insufficient.

【0003】[0003]

【発明が解決しようとする課題】従って、本発明の目的
は皮膚及び毛髪に対して低刺激で、殺菌効果に優れ、さ
らにその持続性も優れた洗浄剤組成物を提供することに
ある。
SUMMARY OF THE INVENTION Therefore, an object of the present invention is to provide a detergent composition which is less irritating to the skin and hair, has an excellent bactericidal effect, and has excellent durability.

【0004】[0004]

【課題を解決するための手段】かかる状況において本発
明者らは鋭意検討をした結果、消炎剤と特定の構造を有
する2級アミド型N−アシルアミノ酸塩を組み合せて配
合することにより、洗浄効果に優れ、皮膚等に対する刺
激がなく、使用感が良好でかつ消炎作用及びその持続性
が良好な洗浄剤組成物が得られることを見出し、本発明
を完成した。
Under the circumstances, as a result of intensive investigations by the present inventors, as a result of adding a combination of an anti-inflammatory agent and a secondary amide type N-acyl amino acid salt having a specific structure, a cleaning effect is obtained. The present invention has been completed by finding that it is possible to obtain a cleansing composition which is excellent in anti-inflammatory properties, has no irritation to the skin, has a good feeling in use, and has an excellent anti-inflammatory effect and its durability.

【0005】すなわち、本発明は次の成分(A)及び
(B) (A)次の一般式(1)で表わされる2級アミド型N−
アシルアミノ酸塩 R1CONH(CH2)nCOOM1 (1) (式中、R1COは炭素数10〜16の直鎖アシル基を
示し、nは1又は2の数を示し、M1はnが1のときは
ナトリウム、カリウム又はアルカノールアンモニウム
を、nが2のときはカリウム又はアルカノールアンモニ
ウムを示す) (B)消炎剤 を含有することを特徴とする洗浄剤組成物を提供するも
のである。
That is, the present invention provides the following components (A) and (B) (A) a secondary amide type N- represented by the following general formula (1).
Acyl amino acid salt R 1 CONH (CH 2 ) n COOM 1 (1) (In the formula, R 1 CO represents a linear acyl group having 10 to 16 carbon atoms, n represents a number of 1 or 2, and M 1 represents When n is 1, sodium, potassium or alkanolammonium is shown, and when n is 2, potassium or alkanolammonium is shown. (B) An anti-inflammatory agent is contained in the detergent composition. ..

【0006】本発明に用いられる(A)成分の2級アミ
ド型N−アシルアミノ酸塩は、水道水中等に含まれるカ
ルシウムと反応して潤滑性の高い板状結晶を生成する性
質を有するため、これを配合した洗浄剤組成物に洗浄後
の滑り等の良好な使用感を付与する作用を示すものであ
る。ここで、2級アミド型N−アシルアミノ酸塩とカル
シウムの反応により生成する板状結晶の潤滑性は、例え
ば乾燥豚皮(アロアスク、抗体化成工業製)を生理食塩
水で再生したものの上における板状結晶の静摩擦係数を
測定することにより求められ、該係数が含水時から乾燥
までブランクの場合より低いものを良好と評価する。ま
た、本発明においては、2級アミド型N−アシルアミノ
酸塩は、板状結晶を生成する際消炎剤をとり込んで結晶
化し、それが皮膚等に付着し、容易に流れ落ちないた
め、消炎剤が少量でも消炎効果を奏し、その持続性も良
好となる。
The secondary amide type N-acyl amino acid salt of the component (A) used in the present invention has the property of reacting with calcium contained in tap water or the like to form a plate crystal with high lubricity. It exhibits the effect of imparting a good feeling of use such as slippage after washing to a detergent composition containing this. Here, the lubricity of the plate-like crystals produced by the reaction of the secondary amide type N-acyl amino acid salt and calcium is, for example, the plate on which dried pork skin (Aloask, manufactured by Antibody Chemical Industries) is regenerated with physiological saline. It is determined by measuring the coefficient of static friction of crystal-like crystals, and those having a coefficient lower than that of the blank from the time of containing water to the time of drying are evaluated as good. Further, in the present invention, the secondary amide type N-acyl amino acid salt incorporates an anti-inflammatory agent during the production of plate crystals to be crystallized, which adheres to the skin or the like and does not easily flow off. It has an anti-inflammatory effect even with a small amount, and its durability is also good.

【0007】上記2級アミド型N−アシルアミノ酸塩に
おいて、前記一般式(1)中、R1COで示される直鎖
アシル基の炭素数は10〜16であり、特に12〜14
であることが望ましく、具体的にはカプリノイル基、ラ
ウロイル基又はミリストイル基が好ましい。この炭素数
が16を超えると、生成する板状結晶の潤滑性が低下す
るため好ましくなく、炭素数が10未満であると、泡立
ちが低下するため好ましくない。また、上記2級アミド
型N−アシルアミノ酸塩は、N−アシル基が上記直鎖の
アシルで構成される2級アミド型構造であることが非常
に重要である。すなわち、N−アシル基を構成するアシ
ル基が分岐状であったり、又はアミド構造が3級アミド
型の場合は、板状結晶の生成が抑制されたり、生成した
結晶の物性が潤滑性に乏しく、べたつきの多いものであ
ったりするため好ましい感触が得難い。また、一般式
(1)中、nが2であり、M1がナトリウム塩であるも
のは、クラフト点が高く、水溶性に劣るため、液体洗浄
剤に用いる場合には好ましくない。
In the above-mentioned secondary amide type N-acyl amino acid salt, in the general formula (1), the linear acyl group represented by R 1 CO has 10 to 16 carbon atoms, particularly 12 to 14 carbon atoms.
Is preferable, and specifically, a caprinoyl group, a lauroyl group, or a myristoyl group is preferable. When the number of carbon atoms exceeds 16, it is not preferable because the lubricity of the plate-like crystals to be formed is lowered, and when the number of carbon atoms is less than 10, foaming is lowered, which is not preferable. In addition, it is very important that the secondary amide type N-acyl amino acid salt has a secondary amide type structure in which the N-acyl group is composed of the linear acyl. That is, when the acyl group constituting the N-acyl group is branched or the amide structure is a tertiary amide type, the production of plate crystals is suppressed, and the physical properties of the produced crystals are poor in lubricity. However, it is difficult to obtain a desirable feeling because it is sticky. Further, in the general formula (1), the one in which n is 2 and M 1 is a sodium salt has a high Kraft point and is inferior in water solubility, so that it is not preferable when used in a liquid detergent.

【0008】本発明に用いられる消炎剤(B)として
は、消炎効果を示し、身体に適用可能なものであればい
ずれも用いることができ、例えばアラントイン、イクタ
モール、グアイアズレン、グリチルリチン酸又はその
塩、グリチルレチン酸、グリチルレチン酸ステアリル、
ステアリン酸グリチルレチニル、イプシロンアミノカプ
ロン酸、フルフェナム酸ブチル、アズレン、カンファ
ー、塩化亜鉛、亜鉛華、メントール、インドメタシン、
イブプロフェンピコノール、メフェナム酸、アロエ末な
どが挙げられるが、これらのうち特にアラントイン、グ
リチルリチン酸ジカリウム、グリチルリチン酸モノアン
モニウム、グリチルレチン酸が好ましい。これらの消炎
剤は、水又は水−低級アルコール等の溶媒に配合して使
用される。
As the anti-inflammatory agent (B) used in the present invention, any anti-inflammatory agent having an anti-inflammatory effect and applicable to the body can be used. For example, allantoin, ictamol, guaiazulene, glycyrrhizic acid or a salt thereof, Glycyrrhetinic acid, stearyl glycyrrhetinate,
Glycyrrhetinyl stearate, epsilon aminocaproic acid, butyl flufenamic acid, azulene, camphor, zinc chloride, zinc white, menthol, indomethacin,
Examples thereof include ibuprofen piconol, mefenamic acid, and aloe powder. Of these, allantoin, dipotassium glycyrrhizinate, monoammonium glycyrrhizinate, and glycyrrhetinic acid are particularly preferred. These anti-inflammatory agents are used by blending with water or a solvent such as water-lower alcohol.

【0009】本発明の洗浄剤組成物における成分(A)
の配合量は、洗浄剤組成物の剤型により異なるが液状洗
浄剤の場合組成物中5〜50重量%、ペースト状洗浄剤
の場合15〜70重量%、固形洗浄剤の場合40〜95
重量%であることが好ましい。成分(B)の配合量はい
ずれの剤型の場合も0.01〜5重量%、特に0.05
〜2重量%が好ましい。
Component (A) in the cleaning composition of the present invention
The compounding amount depends on the formulation of the detergent composition, but is 5 to 50% by weight in the composition for liquid detergent, 15 to 70% by weight for paste detergent, and 40 to 95 for solid detergent.
It is preferably in the weight%. The compounding amount of the component (B) is 0.01 to 5% by weight, especially 0.05 in any dosage form.
~ 2 wt% is preferred.

【0010】本発明の洗浄剤組成物には、さらに高級脂
肪酸塩(C)を配合することにより、前記の特性に加
え、さらに起泡性が良好で泡の感触も良好な洗浄剤が得
られる。ここで、高級脂肪酸塩(C)としては、例えば
炭素数8〜22の脂肪酸の塩基塩が挙げられる。具体的
には、ラウリン酸、ミリスチン酸、パルミチン酸、イソ
ステアリン酸、オレイン酸などの単一脂肪酸の他、ヤシ
油脂肪酸、牛脂脂肪酸等の混合脂肪酸の塩基塩を挙げる
ことができる。ここで塩としては、ナトリウム、カリウ
ムなどの無機塩基性塩、アンモニウム塩、モノエタノー
ルアミン塩、ジエタノールアミン塩、トリエタノールア
ミン塩、2−アミノ−2−メチルプロパノール、2−ア
ミノ−2−メチルプロパンジオール等のアルカノールア
ミン塩、リジン、アルギニン等の塩基性アミノ酸等が挙
げられる。これらの高級脂肪酸塩(C)は、必ずしも脂
肪酸塩として配合する必要はなく、脂肪酸と塩基を独立
に配合して処方系の中で脂肪酸塩を形成せしめてもよ
い。また、これらの高級脂肪酸塩は、単独で又は2種以
上を混合して用いてもよい。なお、本発明洗浄剤組成物
への高級脂肪酸塩(C)の配合量は、成分(A)の配合
量によって異なり、重量比で(C)/(A)=1/20
〜1/2、特に1/10〜1/3が好ましい。
By adding a higher fatty acid salt (C) to the detergent composition of the present invention, a detergent having a good foaming property and a good feeling of foam in addition to the above characteristics can be obtained. .. Here, examples of the higher fatty acid salt (C) include basic salts of fatty acids having 8 to 22 carbon atoms. Specific examples include single fatty acids such as lauric acid, myristic acid, palmitic acid, isostearic acid and oleic acid, as well as basic salts of mixed fatty acids such as coconut oil fatty acid and tallow fatty acid. Here, as the salt, inorganic basic salts such as sodium and potassium, ammonium salt, monoethanolamine salt, diethanolamine salt, triethanolamine salt, 2-amino-2-methylpropanol, 2-amino-2-methylpropanediol. And basic amino acids such as lysine and arginine. These higher fatty acid salts (C) do not necessarily have to be blended as fatty acid salts, and fatty acids and bases may be blended independently to form fatty acid salts in the formulation system. These higher fatty acid salts may be used alone or in combination of two or more. The blending amount of the higher fatty acid salt (C) in the detergent composition of the present invention depends on the blending amount of the component (A), and the weight ratio is (C) / (A) = 1/20.
It is preferably ½, particularly 1/10 to ⅓.

【0011】本発明の洗浄剤組成物には、その他の界面
活性剤、例えばアルキル硫酸塩、アルキルスルホン酸
塩、ポリオキシエチレンアルキル硫酸塩、アルキルベン
ゼンスルホン酸塩、N−アシルサルコシン塩、N−アシ
ル−N−メチルタウリン塩、アルファオレフィンスルホ
ン酸塩、高級脂肪酸エステルスルホン酸塩、アルキルエ
ーテル酢酸塩、ポリオキシエチレンアルキルエーテル酢
酸塩等のアニオン性界面活性剤、脂肪酸アミド、ポリオ
シキエチレンアルキルエーテル等のノニオン性界面活性
剤、イミダゾリン系、ベタイン系等の両性界面活性剤を
本発明の効果を損なわない範囲において任意に併用する
こともできる。
The detergent composition of the present invention includes other surfactants such as alkyl sulfates, alkyl sulfonates, polyoxyethylene alkyl sulfates, alkylbenzene sulfonates, N-acyl sarcosine salts, and N-acyl. -N-methyl taurine salt, alpha olefin sulfonate, higher fatty acid ester sulfonate, anionic surfactant such as alkyl ether acetate, polyoxyethylene alkyl ether acetate, fatty acid amide, polyoxyethylene alkyl ether, etc. Amphoteric surfactants such as nonionic surfactants, imidazoline-based compounds, betaine-based surfactants and the like can be optionally used in combination as long as the effects of the present invention are not impaired.

【0012】さらに、その他の添加剤として、洗浄剤に
通常用いられる成分を本発明の効果を損なわない範囲で
任意に併用することができる。例えば、プロピレングリ
コール、ソルビトール、グリセリン等の保湿剤、カルボ
キシビニルポリマー、メチルセルロース、エタノール、
ポリオキシエチレングリコールジステアレート等の粘度
調整剤、パール化剤、香料、色素、紫外線吸収剤、酸化
防止剤、殺菌剤、防腐剤などを配合することができる。
Further, as other additives, components usually used in detergents can be optionally used in combination within a range that does not impair the effects of the present invention. For example, propylene glycol, sorbitol, humectants such as glycerin, carboxyvinyl polymer, methyl cellulose, ethanol,
Viscosity modifiers such as polyoxyethylene glycol distearate, pearlizing agents, fragrances, dyes, ultraviolet absorbers, antioxidants, bactericides and preservatives can be added.

【0013】本発明の洗浄剤組成物は、常法により製造
され、ペースト状、ゲル状、液状、固形状等の剤型とす
ることができ、皮膚又は毛髪等の身体用の洗浄剤として
適するものであり、特に皮膚洗浄用とするのが好まし
い。
The detergent composition of the present invention is manufactured by a conventional method and can be made into a paste form, a gel form, a liquid form, a solid form or the like, and is suitable as a detergent for the body such as skin or hair. In particular, it is preferably used for cleaning the skin.

【0014】[0014]

【実施例】次に、本発明を実施例に基づいて具体的に詳
述する。但し、本発明は以下に示す実施例に限定される
ものではない。
EXAMPLES Next, the present invention will be described in detail based on examples. However, the present invention is not limited to the examples shown below.

【0015】実施例1 下記の表1に記載の配合組成よりなる洗浄剤組成物を調
製し、これらの洗浄剤組成物について、消炎効果を下記
方法により測定し、また使用感を下記方法及び基準に基
づいて評価した。その結果を下記の表1に示す。なお、
No.6〜11の洗浄剤組成物は比較品である。
Example 1 A detergent composition having the blending composition shown in Table 1 below was prepared, and the anti-inflammatory effect of these detergent compositions was measured by the following method, and the feeling of use was determined by the following method and criteria. It was evaluated based on. The results are shown in Table 1 below. In addition,
No. The detergent compositions of 6 to 11 are comparative products.

【0016】(消炎効果試験法)人前腕部を洗浄剤組成
物1gで洗浄し、水道水で十分にすすぐ。乾燥後、3cm
のガラス製のカップを前腕部に密着させ、エタノール水
溶液(25%)2mlを用いて皮膚に吸着した消炎剤を抽
出する。溶液中の消炎剤量を液体クロマトグラフィーに
て定量し、比較品No.6の値を1.0とした相対比で
示した。さらに8時間後に同操作を行なった。
(Test method for anti-inflammatory effect) A human forearm is washed with 1 g of the detergent composition and thoroughly rinsed with tap water. After drying, 3 cm
The glass cup of 3 is brought into close contact with the forearm, and the anti-inflammatory agent adsorbed on the skin is extracted with 2 ml of an aqueous ethanol solution (25%). The amount of the anti-inflammatory agent in the solution was quantified by liquid chromatography, and the comparative product No. The value of 6 was shown as a relative ratio with the value of 1.0. The same operation was performed 8 hours later.

【0017】(使用感の評価)各洗浄剤組成物につい
て、男女各10名のパネラーに身体の洗浄をさせ、その
際の官能評価を行った。評価は次の基準による平均値を
算出し、平均値が4.5以上の場合を非常に良好
(◎)、3.5〜4.4の場合を良好(○)、2.5〜
3.4の場合をふつう(△)、2.4以下の場合を不良
(×)と判定した。 (1)すすぎ時の泡切れ 5;泡切れが良い 4;泡切れがやや良い 3;ふつう 2;泡切れがやや悪い 1;泡切れが悪い (2)すすぎ時の滑り、(3)すすぎ後の滑り及び
(4)乾燥後の滑り 5;滑りが良い 4;滑りがやや良い 3;ふつう 2;滑りがやや悪い 1;滑りが悪い
(Evaluation of Feel of Use) With respect to each detergent composition, the body was washed by 10 panelists of 10 men and women, and sensory evaluation was performed. For evaluation, an average value was calculated according to the following criteria. When the average value was 4.5 or more, it was very good (⊚), when 3.5 to 4.4, it was good (∘), and 2.5 to
The case of 3.4 was judged to be normal (Δ), and the case of 2.4 or less was judged to be defective (x). (1) Defoaming during rinsing 5; Good defoaming 4; Good defoaming 3; Normal 2; Bad defoaming 1; Bad defoaming (2) Sliding during rinsing, (3) After rinsing And (4) slippage after drying 5; good slippage 4; good slippage 3; normal 2; poor slippage 1; bad slippage

【0018】[0018]

【表1】 [Table 1]

【0019】実施例2 (配合組成) (重量%) (1)ラウロイル−β−アラニントリエタノールアミン 25 (2)グリチルリチン酸ジカリウム 0.3 (3)ラウリン酸トリエタノールアミン 4 (4)ミリスチン酸トリエタノールアミン 2 (5)香料 0.5 (6)ジブチルヒドロキシトルエン 0.2 (7)エタノール 3 (8)精製水 バランス 上記配合組成に従い、加熱水に上記(1)〜(4)成分
を溶解し、冷却後、上記(5)〜(7)成分を添加し、
液体状洗浄剤組成物を調製した。得られた洗浄剤組成物
で身体を洗浄したところ、消炎力が高いため肌荒れ防止
効果に優れ、また、泡立ち及び泡切れが良く、且つすす
ぎ時から乾燥後まで滑りが良く、使用感に優れていた。
Example 2 (Compounding composition) (% by weight) (1) Lauroyl-β-alanine triethanolamine 25 (2) Dipotassium glycyrrhizinate 0.3 (3) Triethanolamine laurate 4 (4) Trimyristate Ethanolamine 2 (5) Fragrance 0.5 (6) Dibutylhydroxytoluene 0.2 (7) Ethanol 3 (8) Purified water balance According to the above composition, the above components (1) to (4) are dissolved in heated water. After cooling, the above components (5) to (7) are added,
A liquid detergent composition was prepared. When the body was washed with the obtained detergent composition, it was excellent in the effect of preventing skin roughening due to its high anti-inflammatory power, and also had good foaming and defoaming, and had good slipperiness from the time of rinsing to the time of drying, and was excellent in usability. It was

【0020】実施例3 (配合組成) (重量%) (1)ラウロイル−β−アラニンK 20 (2)アラントイン 0.5 (3)ラウリン酸K 2 (4)ミリスチン酸K 2 (5)香料 0.5 (6)ジブチルヒドロキシトルエン 0.3 (7)エタノール 4 (8)精製水 バランス 上記配合組成に従い、加熱水に上記(1)〜(4)成分
を溶解し、冷却後、上記(5)〜(7)成分を添加し、
液体状洗浄剤組成物を調製した。得られた洗浄剤組成物
で身体を洗浄したところ、消炎力が高いため肌荒れ防止
効果に優れ、また、泡立ち及び泡切れが良く、且つすす
ぎ時から乾燥後まで滑りが良く、使用感に優れていた。
Example 3 (Composition) (% by weight) (1) Lauroyl-β-alanine K 20 (2) Allantoin 0.5 (3) Lauric acid K 2 (4) Myristic acid K 2 (5) Perfume 0 .5 (6) Dibutylhydroxytoluene 0.3 (7) Ethanol 4 (8) Purified water balance According to the above composition, the above components (1) to (4) are dissolved in heated water, and after cooling, the above (5) ~ (7) component is added,
A liquid detergent composition was prepared. When the body was washed with the obtained detergent composition, it was excellent in the effect of preventing skin roughening due to its high anti-inflammatory power, and also had good foaming and defoaming, and had good slipperiness from the time of rinsing to the time of drying, and was excellent in usability. It was

【0021】[0021]

【発明の効果】本発明洗浄剤組成物は洗浄力が高く、使
用感が良好であり、皮膚及び毛髪に対して刺激性が低い
だけでなく、消炎効果及びその持続性の良いものであ
り、特に皮膚洗浄用に好適である。
EFFECTS OF THE INVENTION The detergent composition of the present invention has high detergency, good feeling in use, low irritation to skin and hair, and good anti-inflammatory effect and its durability. It is particularly suitable for cleaning the skin.

───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.5 識別記号 庁内整理番号 FI 技術表示箇所 C11D 3:32) (C11D 10/02 1:10 3:22) (C11D 10/02 1:10 3:32 1:04) (C11D 10/02 1:10 3:22 1:04) ─────────────────────────────────────────────────── ─── Continuation of the front page (51) Int.Cl. 5 Identification code Office reference number FI technical display location C11D 3:32) (C11D 10/02 1:10 3:22) (C11D 10/02 1:10 3:32 1:04) (C11D 10/02 1:10 3:22 1:04)

Claims (2)

【特許請求の範囲】[Claims] 【請求項1】 次の成分(A)及び(B) (A)次の一般式(1)で表わされる2級アミド型N−
アシルアミノ酸塩 R1CONH(CH2)nCOOM1 (1) (式中、R1COは炭素数10〜16の直鎖アシル基を
示し、nは1又は2の数を示し、M1はnが1のときは
ナトリウム、カリウム又はアルカノールアンモニウム
を、nが2のときはカリウム又はアルカノールアンモニ
ウムを示す) (B)消炎剤 を含有することを特徴とする洗浄剤組成物。
1. The following components (A) and (B) (A) A secondary amide type N- represented by the following general formula (1):
Acyl amino acid salt R 1 CONH (CH 2 ) n COOM 1 (1) (In the formula, R 1 CO represents a linear acyl group having 10 to 16 carbon atoms, n represents a number of 1 or 2, and M 1 represents When n is 1, it represents sodium, potassium or alkanolammonium, and when n is 2, it represents potassium or alkanolammonium.) (B) An anti-inflammatory agent is contained in the detergent composition.
【請求項2】 さらに(C)高級脂肪酸塩を含有するも
のである請求項1記載の洗浄剤組成物。
2. The cleaning composition according to claim 1, further comprising (C) a higher fatty acid salt.
JP32069691A 1991-12-04 1991-12-04 Detergent composition Expired - Fee Related JP3087401B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP32069691A JP3087401B2 (en) 1991-12-04 1991-12-04 Detergent composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP32069691A JP3087401B2 (en) 1991-12-04 1991-12-04 Detergent composition

Publications (2)

Publication Number Publication Date
JPH05156297A true JPH05156297A (en) 1993-06-22
JP3087401B2 JP3087401B2 (en) 2000-09-11

Family

ID=18124325

Family Applications (1)

Application Number Title Priority Date Filing Date
JP32069691A Expired - Fee Related JP3087401B2 (en) 1991-12-04 1991-12-04 Detergent composition

Country Status (1)

Country Link
JP (1) JP3087401B2 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2007297382A (en) * 2006-03-21 2007-11-15 Access Business Group Internatl Llc Method for reducing skin reaction

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2007297382A (en) * 2006-03-21 2007-11-15 Access Business Group Internatl Llc Method for reducing skin reaction

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Publication number Publication date
JP3087401B2 (en) 2000-09-11

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