JP3024821B2 - Detergent composition - Google Patents
Detergent compositionInfo
- Publication number
- JP3024821B2 JP3024821B2 JP3148748A JP14874891A JP3024821B2 JP 3024821 B2 JP3024821 B2 JP 3024821B2 JP 3148748 A JP3148748 A JP 3148748A JP 14874891 A JP14874891 A JP 14874891A JP 3024821 B2 JP3024821 B2 JP 3024821B2
- Authority
- JP
- Japan
- Prior art keywords
- carbon atoms
- group
- alkyl
- same meaning
- alkylene
- 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 - Fee Related
Links
Description
【0001】[0001]
【産業上の利用分野】本発明は洗浄剤組成物、更に詳細
には優れた起泡性と泡持続性を有し、かつ皮膚等に対し
刺激性の少ない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 particularly to a detergent composition having excellent foaming properties and foam sustainability and having little irritation to the skin and the like.
【0002】[0002]
【従来の技術】従来、高級脂肪酸塩は石けん等の洗浄成
分として広く用いられている。例えばラウリン酸カリウ
ムは液体石けんとしてよく用いられており、ミリスチン
酸カリウムは遊離の脂肪酸とともにクリーム状洗浄剤に
好んで用いられている。しかし、これらの成分はアルカ
リ性であるため肌、目等に乾燥感や刺激感を与えるとい
う問題がある。2. Description of the Related Art Hitherto, higher fatty acid salts have been widely used as cleaning components for soaps and the like. For example, potassium laurate is often used as a liquid soap, and potassium myristate is used together with free fatty acids in cream-like detergents. However, since these components are alkaline, there is a problem that they give a dry feeling or a irritating feeling to skin, eyes and the like.
【0003】一方、糖系界面活性剤は皮膚に対する刺激
性が少ないという特長を有するが、これを単独で用いた
場合には起泡性、洗浄性が充分でないという問題があっ
た。そこで、糖系界面活性剤と他の界面活性剤とを併用
する試みも数多く提案されている(特開昭64-69690号、
特開平1-168613号、同1-178596号、同1-178597号、同1-
287198号)。これらの併用系の洗浄剤のうち、糖系界面
活性剤と高級脂肪酸塩との併用系は、洗浄力及び起泡性
が良好であり、かつ刺激性も低いものである。[0003] On the other hand, sugar surfactants have the feature of being less irritating to the skin, but when used alone, there has been a problem that foaming properties and detergency are not sufficient. Therefore, many attempts have been made to use sugar surfactants in combination with other surfactants (JP-A-64-69690,
JP-A Nos. 1-168613, 1-178596, 1-178597, 1-
287198). Among these combined detergents, the combined detergent of a sugar-based surfactant and a higher fatty acid salt has good detergency and foaming property, and has low irritation.
【0004】[0004]
【発明が解決しようとする課題】しかしながら、この糖
系界面活性剤と高級脂肪酸塩を含有する洗浄剤によって
生ずる泡は、泡質が粗く、かつ持続性に劣るものであっ
た。従って、洗浄力及び起泡性に優れ、その泡質が良好
で、泡の持続性に優れ、かつ刺激性の少ない洗浄剤が望
まれていた。However, the foam produced by the detergent containing the saccharide-based surfactant and the higher fatty acid salt has a coarse foam quality and poor durability. Accordingly, there has been a demand for a detergent which is excellent in detergency and foaming properties, has good foam quality, is excellent in foam persistence, and has little irritation.
【0005】[0005]
【課題を解決するための手段】かかる実状において、本
発明者らは上記課題を解決すべく鋭意研究した結果、糖
系界面活性剤及び高級脂肪酸塩に加えて両性界面活性剤
を配合すれば、洗浄力及び起泡性に優れ、かつ皮膚等に
対する刺激性が少なく、更に良好な泡が持続する洗浄剤
が得られることを見出し、本発明を完成した。Under these circumstances, the present inventors have conducted intensive studies to solve the above-mentioned problems, and as a result, if an amphoteric surfactant is added in addition to a sugar-based surfactant and a higher fatty acid salt, The present inventors have found that a cleaning agent which is excellent in detergency and foaming property, has little irritation to skin and the like, and can maintain good foaming can be obtained.
【0006】すなわち、本発明は次の成分(A)、
(B)及び(C) (A)高級脂肪酸塩 (B)一般式(1)That is, the present invention provides the following component (A):
(B) and (C) (A) Higher fatty acid salt (B) General formula (1)
【0007】[0007]
【化2】 Embedded image
【0008】〔式中、R1 は炭素数8〜18の直鎖又は
分岐鎖のアルキル、アルケニル又はアルキルフェニル基
を示し、R2 は炭素数2〜4のアルキレン基を示し、G
は炭素数5〜6の還元糖を示し、mは0〜10の数を示
し、nは1〜10の数を示す〕で表わされる糖系界面活
性剤 (C)一般式(2)、(3)及び(4)で表わされるベ
タイン型両性界面活性剤並びに一般式(5)、(6)及
び(7)で表わされるスルホン酸型両性界面活性剤から
選ばれる両性界面活性剤Wherein R 1 represents a linear or branched alkyl, alkenyl or alkylphenyl group having 8 to 18 carbon atoms, R 2 represents an alkylene group having 2 to 4 carbon atoms,
Represents a reducing sugar having 5 to 6 carbon atoms, m represents a number of 0 to 10 and n represents a number of 1 to 10]. (C) a saccharide-based surfactant represented by the general formula (2), Betaine type amphoteric surfactants represented by 3) and (4) and sulfonic acid type amphoteric surfactants represented by general formulas (5), (6) and (7)
【化8】 〔式中、R3 は炭素数8〜24のアルキル、アルケニ
ル、β−ヒドロキシアルキル又はβ−ヒドロキシアルケ
ニル基を示し、R4 は炭素数1〜4のアルキル基を示
し、R5 は炭素数1〜6のアルキレン又はヒドロキシア
ルキレン基を示す〕Embedded image [Wherein, R 3 represents an alkyl, alkenyl, β-hydroxyalkyl or β-hydroxyalkenyl group having 8 to 24 carbon atoms, R 4 represents an alkyl group having 1 to 4 carbon atoms, and R 5 represents 1 carbon atom. To 6 alkylene or hydroxyalkylene groups]
【化9】 〔式中、R3 及びR5 は前記と同じ意味を有し、pは1
〜20の整数を示す〕Embedded image Wherein R 3 and R 5 have the same meaning as described above, and p is 1
Represents an integer of ~ 20]
【化10】 〔式中、R3 及びR5 は前記と同じ意味を有し、R6 は
カルボキシアルキル又はヒドロキシアルキル基を示す〕Embedded image Wherein R 3 and R 5 have the same meaning as described above, and R 6 represents a carboxyalkyl or hydroxyalkyl group.
【化11】 〔式中、R7 は炭素数7〜19の飽和又は不飽和の炭化
水素基を示し、R8 は炭素数1〜4のアルキレン基を示
し、R9 は炭素数1〜5のアルキル基を示し、R10は炭
素数1〜4のアルキレン又はヒドロキシアルキレン基を
示す〕Embedded image [Wherein, R 7 represents a saturated or unsaturated hydrocarbon group having 7 to 19 carbon atoms, R 8 represents an alkylene group having 1 to 4 carbon atoms, and R 9 represents an alkyl group having 1 to 5 carbon atoms. R 10 represents an alkylene or hydroxyalkylene group having 1 to 4 carbon atoms]
【化12】 〔式中、R7 及びR10は前記と同じ意味を有し、R11及
びR12はそれぞれ炭素数2〜8又は炭素数1〜5のアル
キル又はアルケニル基を示す〕Embedded image [Wherein, R 7 and R 10 have the same meaning as described above, and R 11 and R 12 each represent an alkyl or alkenyl group having 2 to 8 carbon atoms or 1 to 5 carbon atoms]
【化13】 〔式中、R7 及びR10は前記と同じ意味を有し、qは1
〜20の整数を示す〕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。Embedded image Wherein R 7 and R 10 have the same meaning as described above, and q is 1
Which represents an integer of from 20 to 20].
【0009】本発明に用いられる(A)成分である高級
脂肪酸塩としては、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、やし油脂肪酸、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、カルシウムなどの無機塩
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を示す。これらの
高級脂肪酸塩(A)は、必ずしも脂肪酸塩として配合す
る必要はなく、脂肪酸と塩基を単独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。The higher fatty acid salt as the component (A) used in the present invention includes, for example, base salts of fatty acids having 8 to 22 carbon atoms. Specific examples include base salts of single fatty acids such as lauric acid, myristic acid, palmitic acid, isostearic acid and oleic acid, as well as mixed fatty acids such as coconut oil fatty acids and tallow fatty acids. Here, examples of the salt include inorganic basic salts such as sodium, potassium and calcium, ammonium salts, monoethanolamine salts, diethanolamine salts, triethanolamine salts, 2-amino-2-methylpropanol and 2-amino-2-methyl. It shows alkanolamine salts such as propanediol, and basic amino acids such as lysine and arginine. These higher fatty acid salts (A) do not necessarily need to be compounded as fatty acid salts, but may be formed by mixing a fatty acid and a base alone to form a fatty acid salt in a formulation. These higher fatty acid salts may be used alone or in combination of two or more.
【0010】本発明洗浄剤組成物への(A)成分の配合
量は、剤型により異なるが、1〜90重量%(以下、単
に「%」で示す)、特に1〜50%が好ましい。The amount of component (A) to be added to the cleaning composition of the present invention varies depending on the dosage form, but is preferably 1 to 90% by weight (hereinafter simply referred to as "%"), particularly preferably 1 to 50%.
【0011】(B)成分の糖系界面活性剤としては、式
(1)中R1 が炭素数8〜18、特に10〜14のアル
キル基(ラウリル基、ミリスチル基等)であるものが好
ましい。また、親水基の糖部分は、炭素数5〜6の還元
糖〔(1)式中、G〕を基本単位とする。この還元糖と
しては、グルコース、ガラクトース、フラクトースが好
ましい。更に平均糖重合度nは1〜10であり、就中n
=1〜4が特に好ましい。かかる平均糖重合度nはR1
のアルキル基に由来する物性を考慮して選択するのが望
ましく、例えばR1 が炭素数8〜11の疎水基である場
合はn=1〜1.4 を、炭素数12〜14の疎水基である
場合はn=1.5 〜4.0 を選択するのが好ましい。なお、
平均糖重合度nはプロトン−NMR法で求められる。こ
れらの糖系界面活性剤は、単独で又は2種以上を混合し
て用いることができる。As the saccharide-based surfactant of the component (B), those wherein R 1 in the formula (1) is an alkyl group having 8 to 18 carbon atoms, particularly 10 to 14 carbon atoms (lauryl group, myristyl group, etc.) are preferable. . The sugar moiety of the hydrophilic group has a basic unit of a reducing sugar having 5 to 6 carbon atoms [G in the formula (1)]. As this reducing sugar, glucose, galactose and fructose are preferred. Further, the average degree of sugar polymerization n is 1 to 10, especially n
= 1 to 4 are particularly preferred. The average sugar polymerization degree n is R 1
It is desirable to select in consideration of the physical properties derived from the alkyl group of, for example, when R 1 is a hydrophobic group having 8 to 11 carbon atoms, n = 1 to 1.4, and a hydrophobic group having 12 to 14 carbon atoms. In this case, it is preferable to select n = 1.5 to 4.0. In addition,
The average sugar polymerization degree n is determined by a proton-NMR method. These sugar surfactants can be used alone or in combination of two or more.
【0012】本発明洗浄剤組成物への(B)成分の配合
量は、剤型により異なるが、0.1 〜40%、特に1〜2
0%が好ましい。The amount of the component (B) to be added to the detergent composition of the present invention varies depending on the dosage form, but is 0.1 to 40%, preferably 1 to 2%.
0% is preferred.
【0013】(C)成分の両性界面活性剤は、以下に示
すベタイン型両性界面活性剤及びスルホン酸型両性界面
活性剤から選ばれるものである。 (1)ベタイン型両性界面活性剤 (i)次の一般式(2)で表わされるベタイン型両性界
面活性剤The component (C) amphoteric surfactant is selected from the following betaine-type amphoteric surfactants and sulfonic acid-type amphoteric surfactants. (1) Betaine-type amphoteric surfactant (i) Betaine-type amphoteric surfactant represented by the following general formula (2)
【0014】[0014]
【化3】 Embedded image
【0015】〔式中、R3 は炭素数8〜24のアルキ
ル、アルケニル、β−ヒドロキシアルキル又はβ−ヒド
ロキシアルケニル基を示し、R4 は炭素数1〜4のアル
キル基を示し、R5 は炭素数1〜6のアルキレン又はヒ
ドロキシアルキレン基を示す〕 (ii)次の一般式(3)で表わされるベタイン型両性界
面活性剤Wherein R 3 represents an alkyl, alkenyl, β-hydroxyalkyl or β-hydroxyalkenyl group having 8 to 24 carbon atoms, R 4 represents an alkyl group having 1 to 4 carbon atoms, and R 5 represents Shows an alkylene or hydroxyalkylene group having 1 to 6 carbon atoms.] (Ii) Betaine-type amphoteric surfactant represented by the following general formula (3)
【0016】[0016]
【化4】 Embedded image
【0017】〔式中、R3 及びR5 は前記と同じ意味を
有し、pは1〜20の整数を示す〕(iii)次の一般式
(4)で表わされるベタイン型両性界面活性剤Wherein R 3 and R 5 have the same meaning as described above, and p represents an integer of 1 to 20. (iii) Betaine type amphoteric surfactant represented by the following general formula (4)
【0018】[0018]
【化5】 Embedded image
【0019】〔式中、R3 及びR5 は前記と同じ意味を
有し、R6 はカルボキシアルキル又はヒドロキシアルキ
ル基を示す〕 (2)スルホン酸型両性界面活性剤 (i)次の一般式(5)で表わされるスルホン酸型両性
界面活性剤Wherein R 3 and R 5 have the same meaning as described above, and R 6 represents a carboxyalkyl or hydroxyalkyl group. (2) Sulfonic acid type amphoteric surfactant (i) Sulfonic acid type amphoteric surfactant represented by (5)
【0020】[0020]
【化6】 Embedded image
【0021】〔式中、R7 は炭素数7〜19の飽和又は
不飽和の炭化水素基を示し、R8 は炭素数1〜4のアル
キレン基を示し、R9 は炭素数1〜5のアルキル基を示
し、R 10は炭素数1〜4のアルキレン又はヒドロキシア
ルキレン基を示す〕(ii)次の一般式(6)で表わされ
るスルホン酸型両性界面活性剤[Wherein, R7Is saturated with 7 to 19 carbon atoms or
Represents an unsaturated hydrocarbon group;8Is an alkyl having 1 to 4 carbon atoms
Represents a kylene group;9Represents an alkyl group having 1 to 5 carbon atoms
Then R TenIs alkylene or hydroxya having 1 to 4 carbon atoms
Represents a alkylene group] (ii) represented by the following general formula (6)
Sulfonic acid type amphoteric surfactant
【0022】[0022]
【化7】 Embedded image
【0023】〔式中、R7及びR10は前記と同じ意味を
有し、R11及びR12はそれぞれ炭素数2〜8又は炭素数
1〜5のアルキル又はアルケニル基を示す〕(iii)次
の一般式(7)で表わされるスルホン酸型両性界面活性
剤Wherein R 7 and R 10 have the same meaning as described above, and R 11 and R 12 each represent an alkyl or alkenyl group having 2 to 8 carbon atoms or 1 to 5 carbon atoms. Sulfonic acid type amphoteric surfactant represented by the following general formula (7)
【0024】[0024]
【化8】 Embedded image
【0025】〔式中、R7 及びR10は前記と同じ意味を
有し、qは1〜20の整数を示す〕Wherein R 7 and R 10 have the same meaning as described above, and q represents an integer of 1 to 20.
【0026】これらの(C)成分の両性界面活性剤は、
単独で又は2種以上を混合して用いることができ、その
配合量は、剤型により異なるが0.1 〜30%、特に0.5
〜20%が好ましい。These amphoteric surfactants of component (C) include:
They may be used alone or in admixture of two or more. The compounding amount varies depending on the dosage form, but is 0.1 to 30%, especially 0.5 to 30%.
~ 20% is preferred.
【0027】また、本発明洗浄剤組成物には、上記必須
成分の他に、洗浄剤として通常用いられる成分を発明の
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。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、抗炎症
剤、防腐剤などを配合することができる。The cleaning composition of the present invention may contain, in addition to the above essential components, components commonly used as cleaning agents, as long as the effects of the present invention are not impaired. For example, propylene glycol, sorbitol,
Humectants such as glycerin, carboxyvinyl polymers, viscosity modifiers such as methylcellulose, ethanol and polyoxyethylene glycol distearate, pearling agents, fragrances, dyes, ultraviolet absorbers, antioxidants, bactericides, anti-inflammatory agents, Preservatives and the like can be added.
【0028】本発明洗浄剤組成物の剤型は特に限定され
ないが、特に液状、クリーム状等が好ましい。これらの
液状、クリーム状の剤型の洗浄剤を調製するには、常法
に従い、水性基剤に上記成分を均一に混合・分散せしめ
ればよい。The dosage form of the cleaning composition of the present invention is not particularly limited, but is preferably a liquid, a cream or the like. In order to prepare these liquid and creamy detergents, the above components may be uniformly mixed and dispersed in an aqueous base according to a conventional method.
【0029】[0029]
【発明の効果】本発明の洗浄剤組成物は、洗浄力及び起
泡性に優れ、皮膚に対する刺激性が少なく、かつなめら
かな泡が持続するものであり、特に顔、手等の皮膚洗浄
用及び毛髪洗浄用として有用である。The cleaning composition of the present invention has excellent detergency and foaming properties, has little skin irritation, and maintains a smooth foam, and is particularly useful for cleaning the skin of the face and hands. And it is useful for cleaning hair.
【0030】[0030]
【実施例】次に実施例を挙げて本発明を詳細に説明する
が、本発明はこれに限定されるものではない。Next, the present invention will be described in detail with reference to examples, but the present invention is not limited to these examples.
【0031】実施例1 表1記載の成分を均一に混合して、洗浄剤組成物を調製
した。得られた洗浄剤組成物について、専門パネラー1
0名に手を洗ってもらい、その起泡性、泡の持続性につ
いて官能評価を行った。結果を表1に示す。評価基準 起泡性、泡持続性 非常に良い :◎ 良い :○ あまり良くない:△ わるい :×Example 1 A cleaning composition was prepared by uniformly mixing the components shown in Table 1. About the obtained cleaning composition, a specialized panelist 1
No one had their hands washed, and a sensory evaluation was performed on their foaming properties and foam continuity. Table 1 shows the results. Evaluation criteria Foaming property, foam sustainability Very good: ◎ Good: ○ Not very good: △ Bad: ×
【0032】[0032]
【表1】 [Table 1]
【0033】表1より、(A)、(B)及び(C)の3
成分を配合した本発明洗浄剤組成物は、これらのうちの
2成分を配合した洗浄剤に比べ、起泡性、泡持続性とも
に良好であった。なお、本発明洗浄剤組成物は、洗浄力
が強く、かつ手肌に対する刺激性の極めて弱いものであ
った。From Table 1, three of (A), (B) and (C)
The detergent composition of the present invention in which the components were blended had better foaming properties and foam sustainability than the detergent in which these two components were blended. In addition, the cleaning composition of the present invention had a strong detergency and was extremely irritating to hand skin.
【0034】実施例2(洗顔料) (組成) (%) アルキルサッカライド (R1=C10H21,m=0,G=グルコース,n=2) 10 ミリスチン酸カリウム 20 ラウリルヒドロキシスルホベタイン 3 ラウリルジメチルアミンオキサイド 2 グリセリン 10 BHT(2,6−ジ−t−ブチル−4−メチルフェノール) 0.1 イオン交換水 バランス 合 計 100 Example 2 (facial cleanser) (Composition) (%) Alkyl saccharide (R 1 = C 10 H 21 , m = 0, G = glucose, n = 2) 10 Potassium myristate 20 Laurylhydroxysulfobetaine 3 Lauryl dimethylamine oxide 2 glycerin 10 BHT (2,6-di -t- butyl-4-methylphenol) 0.1 ion exchanged water balance total 100
【0035】実施例3(ボディーシャンプー) (組成) (%) アルキルサッカライド (R1=C10H21,m=0,G=グルコース,n=1.5) 10 ラウリン酸トリエタノールアミン 20 ラウリルジメチルアミノ酢酸ベタイン 3 プロピレングリコール 5 変性エタノール 5 エチレングリコールジステアリル 3 ポリオキシエチレンミリスチルエーテル 1 イオン交換水 バランス 合 計 100 Example 3 (Body shampoo) (Composition) (%) Alkyl saccharide (R 1 = C 10 H 21 , m = 0, G = glucose, n = 1.5) 10 Triethanolamine laurate 20 Lauryldimethylaminoacetic acid Betaine 3 Propylene glycol 5 Denatured ethanol 5 Ethylene glycol distearyl 3 Polyoxyethylene myristyl ether 1 Ion-exchanged water Balance total 100
【0036】実施例4(シャンプー) (組成) (%) ポリオキシエチレンラウリル硫酸ナトリウム 5 アルキルサッカライド (R1=C10H21,m=0,G=グルコース,n=1.5) 5 ステアリン酸トリエタノールアミン 3 ラウリルジメチルスルホベタイン 3 プロピレングリコール 2 イオン交換水 バランス 合 計 100Example 4 (Shampoo) (Composition) (%) Sodium polyoxyethylene lauryl sulfate 5 alkyl saccharide (R 1 = C 10 H 21 , m = 0, G = glucose, n = 1.5) 5 Triethanol stearate amine 3 lauryl dimethyl sulfobetaine 3 propylene glycol 2 ion-exchanged water balance total 100
───────────────────────────────────────────────────── フロントページの続き (56)参考文献 特開 平4−173898(JP,A) 特開 平4−213398(JP,A) (58)調査した分野(Int.Cl.7,DB名) C11D 10/04 C11D 9/02 C11D 1/68 C11D 1/90 ────────────────────────────────────────────────── ─── Continuation of the front page (56) References JP-A-4-173898 (JP, A) JP-A-4-213398 (JP, A) (58) Fields investigated (Int. Cl. 7 , DB name) C11D 10/04 C11D 9/02 C11D 1/68 C11D 1/90
Claims (1)
キル、アルケニル又はアルキルフェニル基を示し、R2
は炭素数2〜4のアルキレン基を示し、Gは炭素数5〜
6の還元糖を示し、mは0〜10の数を示し、nは1〜
10の数を示す〕で表わされる糖系界面活性剤 (C)一般式(2)、(3)及び(4)で表わされるベ
タイン型両性界面活性剤並びに一般式(5)、(6)及
び(7)で表わされるスルホン酸型両性界面活性剤から
選ばれる両性界面活性剤 【化2】 〔式中、R3 は炭素数8〜24のアルキル、アルケニ
ル、β−ヒドロキシアルキル又はβ−ヒドロキシアルケ
ニル基を示し、R4 は炭素数1〜4のアルキル基を示
し、R5 は炭素数1〜6のアルキレン又はヒドロキシア
ルキレン基を示す〕 【化3】 〔式中、R3 及びR5 は前記と同じ意味を有し、pは1
〜20の整数を示す〕 【化4】 〔式中、R3 及びR5 は前記と同じ意味を有し、R6 は
カルボキシアルキル又はヒドロキシアルキル基を示す〕 【化5】 〔式中、R7 は炭素数7〜19の飽和又は不飽和の炭化
水素基を示し、R8 は炭素数1〜4のアルキレン基を示
し、R9 は炭素数1〜5のアルキル基を示し、R10は炭
素数1〜4のアルキレン又はヒドロキシアルキレン基を
示す〕 【化6】 〔式中、R7 及びR10は前記と同じ意味を有し、R11及
びR12はそれぞれ炭素数2〜8又は炭素数1〜5のアル
キル又はアルケニル基を示す〕 【化7】 〔式中、R7 及びR10は前記と同じ意味を有し、qは1
〜20の整数を示す〕を含有することを特徴とする洗浄
剤組成物。1. The following components (A), (B) and (C) (A) higher fatty acid salt (B) general formula (1) [In the formula, R 1 represents a linear or branched alkyl, alkenyl or alkylphenyl group having 8 to 18 carbon atoms, R 2
Represents an alkylene group having 2 to 4 carbon atoms, and G represents 5 to 5 carbon atoms.
6 represents a reducing sugar, m represents a number of 0 to 10, and n represents 1 to
A sugar-based surfactant represented by the general formula (2), (3) or (4), or a betaine-type amphoteric surfactant represented by the general formula (5), (6) or An amphoteric surfactant selected from sulfonic acid type amphoteric surfactants represented by (7) [Wherein, R 3 represents an alkyl, alkenyl, β-hydroxyalkyl or β-hydroxyalkenyl group having 8 to 24 carbon atoms, R 4 represents an alkyl group having 1 to 4 carbon atoms, and R 5 represents 1 carbon atom. Represents an alkylene or hydroxyalkylene group of 1 to 6] Wherein R 3 and R 5 have the same meaning as described above, and p is 1
Represents an integer of from 20 to 20] Wherein R 3 and R 5 have the same meaning as described above, and R 6 represents a carboxyalkyl or hydroxyalkyl group. [Wherein, R 7 represents a saturated or unsaturated hydrocarbon group having 7 to 19 carbon atoms, R 8 represents an alkylene group having 1 to 4 carbon atoms, and R 9 represents an alkyl group having 1 to 5 carbon atoms. And R 10 represents an alkylene or hydroxyalkylene group having 1 to 4 carbon atoms. Wherein R 7 and R 10 have the same meaning as described above, and R 11 and R 12 each represent an alkyl or alkenyl group having 2 to 8 carbon atoms or 1 to 5 carbon atoms. Wherein R 7 and R 10 have the same meaning as described above, and q is 1
Which represents an integer of from 20 to 20].
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP3148748A JP3024821B2 (en) | 1991-06-20 | 1991-06-20 | Detergent composition |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP3148748A JP3024821B2 (en) | 1991-06-20 | 1991-06-20 | Detergent composition |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH04372696A JPH04372696A (en) | 1992-12-25 |
JP3024821B2 true JP3024821B2 (en) | 2000-03-27 |
Family
ID=15459747
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP3148748A Expired - Fee Related JP3024821B2 (en) | 1991-06-20 | 1991-06-20 | Detergent composition |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP3024821B2 (en) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP6482181B2 (en) * | 2014-03-31 | 2019-03-13 | ミヨシ油脂株式会社 | Transparent liquid detergent composition |
JP6717585B2 (en) * | 2014-11-10 | 2020-07-01 | 日本曹達株式会社 | Antibacterial composition |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2728791B2 (en) * | 1990-06-21 | 1998-03-18 | 鐘紡株式会社 | Transparent soap composition |
JPH04173898A (en) * | 1990-11-06 | 1992-06-22 | Kanebo Ltd | Detergent composition |
-
1991
- 1991-06-20 JP JP3148748A patent/JP3024821B2/en not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
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JPH04372696A (en) | 1992-12-25 |
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