JPH07126689A - Detergent - Google Patents

Detergent

Info

Publication number
JPH07126689A
JPH07126689A JP30696693A JP30696693A JPH07126689A JP H07126689 A JPH07126689 A JP H07126689A JP 30696693 A JP30696693 A JP 30696693A JP 30696693 A JP30696693 A JP 30696693A JP H07126689 A JPH07126689 A JP H07126689A
Authority
JP
Japan
Prior art keywords
ester
fatty acid
acid
power
detergent
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.)
Pending
Application number
JP30696693A
Other languages
Japanese (ja)
Inventor
Nobuhiro Mori
信博 森
Tetsuo Kobayashi
哲夫 小林
Ryozo Iwasaki
亮三 岩崎
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.)
Lion Corp
Original Assignee
Lion 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 Lion Corp filed Critical Lion Corp
Priority to JP30696693A priority Critical patent/JPH07126689A/en
Publication of JPH07126689A publication Critical patent/JPH07126689A/en
Pending legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/0005Other compounding ingredients characterised by their effect
    • C11D3/0094High foaming compositions
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/66Non-ionic compounds
    • C11D1/825Mixtures of compounds all of which are non-ionic

Abstract

PURPOSE:To obtain a detergent, capable of increasing foaming power and detergency due to mutual synergistic effects. CONSTITUTION:This detergent contains (A) one or two or more sugar ester- based surfactants comprising 6-22C fatty acids and saccharides selected from disaccharides composed of dihexoses and 4-6C sugaralcohols and (B) one or two or more selected from anionic surfactants having COO<->, OSO3<-> or SO3<-> group at (1/5) to (5/1) (wt./wt.) ratio of the components (A)/(B) in the total amount of the components (A) and (B) within the range of 5-50wt.%.

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、起泡力、乳化力、可溶
化力、分散力等の基本的な界面活性能に優れた洗浄剤に
関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a detergent excellent in basic surface activity such as foaming power, emulsifying power, solubilizing power and dispersing power.

【0002】[0002]

【従来の技術】従来、衣料用洗剤、台所用洗剤、毛髪用
洗剤、身体用洗剤においては、目的とする被洗物の種類
及び汚れの種類に応じた洗浄剤組成が確立され、いずれ
の洗浄剤においても主成分としては、起泡力、乳化力、
可溶化力、分散力などの基本的界面活性能に優れたアニ
オン界面活性剤が主に使用されてきた。更に衣料用洗剤
ではアルカリ剤、キレートビルダー、蛍光剤、漂白剤、
酵素等、台所用洗剤や毛髪用洗剤では脂肪酸アルカノー
ルアミドやアルコールエトキシレート系ノニオン界面活
性剤等が起泡力、洗浄力の観点から併用されてきた。
2. Description of the Related Art Conventionally, for laundry detergents, kitchen detergents, hair detergents, and body detergents, a detergent composition has been established according to the type of object to be washed and the type of stain, and any of these types of detergents can be used. The main ingredients of the agent are foaming power, emulsifying power,
Anionic surfactants having excellent basic surface activity such as solubilizing power and dispersing power have been mainly used. For laundry detergents, alkaline agents, chelating builders, fluorescent agents, bleaching agents,
In kitchen detergents and hair detergents such as enzymes, fatty acid alkanolamides and alcohol ethoxylate nonionic surfactants have been used together from the viewpoint of foaming power and detergency.

【0003】しかしこれらの組み合わせは、各成分の各
性能における積算的結果と同等又はそれ以下にしか過ぎ
ず、主成分のアニオン界面活性剤の能力を増大させる効
果を期待するものではなかった。
However, these combinations are equal to or less than the cumulative results in each performance of each component, and are not expected to have the effect of increasing the ability of the anionic surfactant as the main component.

【0004】[0004]

【発明が解決しようとする課題】本発明は、起泡力、乳
化力、可溶化力、分散力等の基本的界面活性能が要求さ
れる洗浄剤において、その主成分となるアニオン界面活
性剤の界面活性能を増強させ、具体的には起泡力、洗浄
力の向上を目的とする。
DISCLOSURE OF THE INVENTION The present invention relates to an anionic surfactant which is a main component of a detergent which requires basic surface activity such as foaming power, emulsifying power, solubilizing power and dispersing power. The purpose of this is to enhance the surface activity of the, and specifically to improve the foaming power and the cleaning power.

【0005】[0005]

【課題を解決するための手段】本発明者は、上記課題を
解決すべく鋭意検討した結果、(A)炭素数6〜22の
脂肪酸とジヘキソースからなる二糖類、炭素数4〜6の
糖アルコールから選ばれた糖類からなる糖エステル系界
面活性剤の1種又は2種以上と、(B)−COO、−
OSO 又は−SO 基をもつアニオン界面活性剤
から選ばれる1種又は2種以上を、(A)/(B)成分
比が1/5〜5/1(w/w)の比率で組み合わせた場
合、起泡力、洗浄力に強い相乗効果が発揮される事を知
見し、本発明に至ったものである。
Means for Solving the Problems As a result of intensive studies to solve the above problems, the present inventor has (A) a disaccharide consisting of a fatty acid having 6 to 22 carbon atoms and dihexose, and a sugar alcohol having 4 to 6 carbon atoms. One or more sugar ester surfactants composed of saccharides selected from (B) -COO - ,-
A ratio of (A) / (B) component ratio of 1/5 to 5/1 (w / w) of one or more kinds selected from anionic surfactants having an OSO 3 or —SO 3 group. It was discovered that a strong synergistic effect on foaming power and detergency is exhibited when these are combined, and the present invention has been achieved.

【0006】本発明の(A)成分である糖エステル系界
面活性剤は、炭素数6〜22の脂肪酸又は脂肪酸エステ
ルのような脂肪酸誘導体と、二糖類、糖アルコールとか
ら合成される。
The sugar ester type surfactant which is the component (A) of the present invention is synthesized from a fatty acid derivative having 6 to 22 carbon atoms such as a fatty acid or a fatty acid ester, a disaccharide and a sugar alcohol.

【0007】ここで脂肪酸とは、飽和でも不飽和でも、
又直鎖でも分岐を有していてもよい。このような脂肪酸
の具体例としては、例えば、カプロン酸、カプリル酸、
カプリン酸、ラウリン酸、ミリスチン酸、パルミチン
酸、ステアリン酸、カプロレイン酸、ラウロレイン酸、
ミリストレイン酸、パルミトレイン酸、オレイン酸、メ
チルウンデカン酸等が挙げられ、好ましい脂肪酸残基数
は糖アルコール類エステルで炭素数が8〜12のもの、
二糖類エステルで炭素数が10〜14のものである。
Here, the fatty acid, whether saturated or unsaturated,
It may be straight-chain or branched. Specific examples of such fatty acids include, for example, caproic acid, caprylic acid,
Capric acid, lauric acid, myristic acid, palmitic acid, stearic acid, caproic acid, lauroic acid,
Myristoleic acid, palmitoleic acid, oleic acid, methylundecanoic acid and the like can be mentioned. Preferred fatty acid residues are sugar alcohol esters having 8 to 12 carbon atoms,
A disaccharide ester having 10 to 14 carbon atoms.

【0008】又脂肪酸誘導体としては、上記脂肪酸と低
級アルコールとの脂肪酸エステル等が用いられ、例えば
上記脂肪酸のメチルエステル、エチルエステル、プロピ
ルエステル等が挙げられる。
As the fatty acid derivative, a fatty acid ester of the above fatty acid and a lower alcohol is used, and examples thereof include methyl ester, ethyl ester and propyl ester of the above fatty acid.

【0009】ジヘキソースからなる二糖類としては、還
元性二糖としてマルトース、セロビオース、ラクトー
ス、イソマルトース、ゲンチオビオース、ニゲロース、
ソホロース、非還元性二糖としてシュクロース、トレハ
ロース等が挙げられる。
As disaccharides composed of dihexose, reducing disaccharides such as maltose, cellobiose, lactose, isomaltose, gentiobiose, nigerose,
Sophorose and non-reducing disaccharides include sucrose and trehalose.

【0010】糖アルコールとしては、エリスリトール、
リビトール、キシリトール、アリトール、ソルビトー
ル、マンニトール、ガラクチトール等が挙げられる。
As the sugar alcohol, erythritol,
Examples thereof include ribitol, xylitol, allitol, sorbitol, mannitol, galactitol and the like.

【0011】本発明において(A)成分の糖エステル系
界面活性剤は、糖1分子中、脂肪酸残基が1個結合した
モノエステル型を主成分とする事が望ましく、トリエス
テル以上のポリエステルが、1重量%以下である事が望
ましい。
In the present invention, the sugar ester type surfactant as the component (A) is preferably composed mainly of a monoester type in which one fatty acid residue is bonded in one molecule of sugar, and a polyester of triester or more is used. It is preferably 1% by weight or less.

【0012】又、(B)成分のアニオン界面活性剤とし
ては、−COO基を持つ界面活性剤(カルボン酸
系)、−OSO 基を持つ界面活性剤(硫酸エステル
塩系)又は−SO 基を持つ界面活性剤(スルホン酸
塩系)が用いられ、具体例として以下のものが例示でき
る。 (1)カルボン酸塩系アニオン界面活性剤 ・C10〜C18の脂肪酸塩 ・エステル部分の炭素数3〜15のコハク酸モノアルキ
ルエステル塩 ・下記化1で示されるエーテルカルボン酸塩
[0012] Further, as an anionic surfactant (B) component, -COO - surfactant having a group (acid type), - OSO 3 - surfactant having a group (sulfate salt) or - A surfactant having a SO 3 group (sulfonate type) is used, and the following can be mentioned as specific examples. (1) Carboxylate-based anionic surfactant-C 10 to C 18 fatty acid salt-Ester moiety having 3 to 15 carbon atoms succinic acid monoalkyl ester salt-Ether carboxylate represented by the following chemical formula 1

【化1】 [Chemical 1]

【化2】 (2)硫酸エステル系アニオン界面活性剤 ・C10〜C18のアルキル硫酸塩 ・アルキル基又はアルケニル基の炭素数10〜18のア
ルキル(またはアルケニル)ポリエトキシ硫酸塩(エチ
レンオキシドの平均付加モル数p=2〜7) (3)スルホン酸系アニオン界面活性剤 ・C10〜C18のアルカンスルホン酸系 ・C10〜C18のオレフィンスルホン酸系 ・アルキル基の炭素数がC〜C18のアルキルベンゼ
ンスルホン 酸塩系 ・脂肪酸残基の炭素数が8〜20の脂肪酸低級アルキル
エステルのスルホン酸塩(α−スルホ脂肪酸低級アルキ
ルエステル塩):これらの塩としては、アルカリ金属
塩、アルカリ土類金属塩、アンモニウム塩、アルカノー
ルアミン塩等が用いられる。
[Chemical 2] (2) Sulfate ester-based anionic surfactant-C 10 to C 18 alkyl sulfate-Alkyl (or alkenyl) alkyl (or alkenyl) polyethoxysulfate having 10 to 18 carbon atoms (average number of moles of ethylene oxide added p = 2 to 7) (3) Sulfonic acid type anionic surfactant-C 10 to C 18 alkane sulfonic acid type-C 10 to C 18 olefin sulfonic acid type-Alkylbenzene having an alkyl group of C 8 to C 18 Sulfonate-Sulfonates of fatty acid lower alkyl esters having 8 to 20 carbon atoms in the fatty acid residue (α-sulfofatty acid lower alkyl ester salts): These salts include alkali metal salts and alkaline earth metal salts. , Ammonium salts, alkanolamine salts and the like are used.

【0013】又その他に、他のアニオン界面活性剤、ノ
ニオン界面活性剤、カチオン界面活性剤、両性界面活性
剤、アルキルアミンオキシド、アルカノールアミン、脂
肪酸アルカノールアミド、ハイドロトロープ剤、イオン
封鎖剤、抗菌剤、色素、香料等を添加する事ができる。
In addition, other anionic surfactants, nonionic surfactants, cationic surfactants, amphoteric surfactants, alkylamine oxides, alkanolamines, fatty acid alkanolamides, hydrotropes, ion sequestering agents, antibacterial agents. , Dyes, fragrances, etc. can be added.

【0014】本発明の洗浄剤組成物によれば、(A)糖
エステル系界面活性剤の1種または2種以上と、(B)
アニオン界面活性剤の1種または2種以上を、(A)/
(B)成分比が1/5〜5/1(w/w)でかつ、
(A)+(B)が5〜50重量%の範囲で併用すること
により、優れた起泡力と洗浄力を得ることができる。
According to the detergent composition of the present invention, (A) one or more sugar ester surfactants and (B)
One or more of the anionic surfactants are (A) /
(B) component ratio is 1/5 to 5/1 (w / w), and
By using together (A) + (B) in the range of 5 to 50% by weight, excellent foaming power and detergency can be obtained.

【0015】[0015]

【実験例1】オクタノイル−マンニトールエステル及び
オクタノイル−ソルビトールエステルの調製
Experimental Example 1 Preparation of octanoyl-mannitol ester and octanoyl-sorbitol ester

【0016】マンニトール101.1g(0.56mo
le)及びオクタン酸メチル438.5g(2.78m
ole)の混合物に、反応溶媒としてβ−ピコリン50
0gを加え、70℃にて攪拌した。触媒としてキャンデ
ィダアンタークティカ由来固定化リパーゼSP−382
(ノボ社製)を10g添加した。減圧(45mmHg)
下に副生するメタノールをパーシャルコンデンサーによ
り除去しながら攪拌を続けた。5時間後反応を停止し、
酵素を吸引濾過により除去した。反応溶媒と未反応メチ
ルエステルの約3/4を減圧蒸留により除去し、更に4
倍量のヘキサンを用いて再結晶を行った。その結果3%
マンニトールを含むオクタノイル−マンニトールモノエ
ステル(160g)が得られた。生成物中のジエステル
含量は1%以下であった。
Mannitol 101.1 g (0.56 mo
le) and methyl octanoate 438.5 g (2.78 m)
ole) to a mixture of β-picoline 50 as a reaction solvent
0 g was added, and the mixture was stirred at 70 ° C. Immobilized lipase SP-382 derived from Candida antarctica as catalyst
(Novo) was added. Decompression (45 mmHg)
Stirring was continued while removing by-produced methanol by a partial condenser. Stop the reaction after 5 hours,
The enzyme was removed by suction filtration. About 3/4 of the reaction solvent and unreacted methyl ester were removed by vacuum distillation, and
Recrystallization was performed using twice the amount of hexane. As a result, 3%
Octanoyl-mannitol monoester containing mannitol (160 g) was obtained. The diester content in the product was less than 1%.

【0017】マンニトールをソルビトール101.1g
(0.56mole)に変更し、同様の手順によりエス
テル交換反応及びエステルの精製を行った。その結果、
5%ソルビトールを含むオクタノイル−ソルビトールモ
ノエステル(170g)が得られた。生成物中のジエス
テル含量は1%以下であった。
Mannitol and sorbitol 101.1 g
(0.56 mole), and transesterification reaction and ester purification were carried out by the same procedure. as a result,
Octanoyl-sorbitol monoester (170 g) containing 5% sorbitol was obtained. The diester content in the product was less than 1%.

【0018】[0018]

【実験例2】 ドデカノイル−マルトースエステル及びドデカノイル−
シュクロースエステルの調製
Experimental Example 2 Dodecanoyl-maltose ester and dodecanoyl-
Preparation of sucrose ester

【0019】無水マルトース201.8g(0.56m
ole)及びドデカン酸557.0g(2.78mol
e)の混合物に、反応溶媒としてβ−ピコリン700g
を加え、70℃にて攪拌した。触媒として SP−38
2を20g添加した。減圧(50mmHg)下に副生水
をパーシャルコンデンサーにより除去しながら攪拌を続
けた。15時間後反応を停止し、酵素を吸引濾過により
除去した。得られた反応溶液から、反応溶媒を通常の減
圧蒸留(90℃、1mmHg)により除去し、さらに5
倍量のヘキサンを用いて再結晶を行った。その結果1%
マルトースを含むドデカノイル−マルトースモノエステ
ル(280g)が得られた。生成物中のジエステル含量
は1%以下であった(GLC分析)。
201.8 g (0.56 m) of anhydrous maltose
ole) and dodecanoic acid 557.0 g (2.78 mol)
700 g of β-picoline as a reaction solvent in the mixture of e)
Was added and stirred at 70 ° C. As catalyst SP-38
20 g of 2 was added. Stirring was continued while removing by-product water with a partial condenser under reduced pressure (50 mmHg). The reaction was stopped after 15 hours and the enzyme was removed by suction filtration. From the obtained reaction solution, the reaction solvent was removed by ordinary vacuum distillation (90 ° C., 1 mmHg), and further 5
Recrystallization was performed using twice the amount of hexane. As a result, 1%
Dodecanoyl-maltose monoester with maltose (280 g) was obtained. The diester content in the product was below 1% (GLC analysis).

【0020】マルトースをシュクロース191.7g
(0.56mole)に変更し、同様の手順によりエス
テルを作成した。その結果、0.5%シュクロースを含
むデカノイル−シュクロースモノエステル(270g)
が得られた。
191.7 g of sucrose with maltose
(0.56 mole) was changed, and an ester was prepared by the same procedure. As a result, decanoyl-sucrose monoester containing 0.5% sucrose (270 g)
was gotten.

【0021】実験例1、2で得られた各種糖エステル系
界面活性剤を用い、以下の実施例で本発明を実証する。
The present invention is demonstrated in the following examples using the various sugar ester type surfactants obtained in Experimental Examples 1 and 2.

【0022】[0022]

【実施例1】 −起泡力試験− 毛髪洗浄剤用のモデル汚垢として、液体ラノリン0.2
gをエプトン管(100ml)に採る。更に(a)0.
9%糖エステル界面活性剤10mlと(b)0.9%ア
ニオン界面活性剤10mlを加え、室温で10秒間に2
0回振盪する。水溶液と起泡界面が明確になった時点で
の泡高(ml)を測定した。結果を表1に示す。
[Example 1] -Foaming test-Liquid lanolin 0.2 was used as a model soil for hair cleansing agents.
Collect g in an Epton tube (100 ml). Further (a) 0.
Add 10 ml of 9% sugar ester surfactant and 10 ml of (b) 0.9% anionic surfactant, and add 2 for 10 seconds at room temperature.
Shake 0 times. The foam height (ml) at the time when the interface between the aqueous solution and the foaming became clear was measured. The results are shown in Table 1.

【0023】[0023]

【実施例2〜8、比較例1〜3】表2に示す組成の液体
洗浄剤組成物を調製し、油性汚垢洗浄力、バター汚垢洗
浄力を下記方法で評価した。結果を表2に併記する。
Examples 2 to 8 and Comparative Examples 1 to 3 Liquid detergent compositions having the compositions shown in Table 2 were prepared and the oily dirt cleaning power and butter dirt cleaning power were evaluated by the following methods. The results are also shown in Table 2.

【0024】−油性汚垢洗浄力− 日本薬局方に規定された大豆油と牛脂各10gを60m
lのクロロホルムに溶解した後、オイルレッド0.1g
を加えてよく混合し、汚垢溶液を調製する。この溶液に
ガラスプレートを浸して汚染し、25℃の温度で30分
以上風乾してクロロホルムを除去し、汚垢片を作成する
(汚垢量20〜23mg/枚)。この汚垢片6枚を25
℃、700mlの0.15重量%の洗浄剤液中で250
rpmの回転速度で3分間かき混ぜて洗浄した後、風乾
して重量を測定し、洗浄後の油除去率を下記の式により
算出して洗浄力とした。
-Determination of oily dirt-Soybean oil and beef tallow 10g each specified by the Japanese Pharmacopoeia 60m
0.1 g of oil red after dissolving in l of chloroform
Add and mix well to prepare a soil solution. A glass plate is soaked in this solution to contaminate it and air-dried at a temperature of 25 ° C. for 30 minutes or more to remove chloroform to prepare a piece of dirt (amount of dirt 20 to 23 mg / sheet). 25 pieces of 6 pieces of this dirt
250 in 700 ml of 0.15 wt% detergent solution
After washing by stirring for 3 minutes at a rotation speed of rpm, air drying was performed and the weight was measured, and the oil removal rate after washing was calculated by the following formula to obtain the washing power.

【0025】−バター汚垢洗浄力− 組成物0.15重量%を含む水溶液を調製し、その3リ
ットルを直径30cm、深さ12cmのバットに入れ、
液温25℃において空気を含んだスポンジを液中で圧縮
する操作を10回繰り返して泡立てたのち、1枚あたり
0.5gのバターを塗布した皿の表面を10回、裏面を
5回ずつスポンジで擦り洗いし、泡高が3mmになるま
でに洗える皿の枚数を洗浄力とした。
-Butter dirt cleaning power- An aqueous solution containing 0.15% by weight of the composition was prepared, and 3 liters thereof were placed in a vat having a diameter of 30 cm and a depth of 12 cm,
The operation of compressing the air-containing sponge in the liquid at a liquid temperature of 25 ° C is repeated 10 times to create a foam, and then 0.5 g of butter is applied to each side of the dish 10 times and the back side is 5 times each. The washing power was defined as the number of dishes that could be washed until the foam height reached 3 mm.

【0026】[0026]

【実施例9〜11、比較例4〜6】 −洗濯実験− 界面活性剤15%(非イオン性/LAS=1/1)、ゼ
オライト15%、炭酸カリウム20%、Ash50%か
らなる重質粉末洗剤を調製し、8.3g/lの濃度で洗
濯実験を行った。
Examples 9 to 11 and Comparative Examples 4 to 6 -Washing Experiment- Heavy powder consisting of 15% surfactant (nonionic / LAS = 1/1), 15% zeolite, 20% potassium carbonate, and 50% Ash. A detergent was prepared and a washing experiment was conducted at a concentration of 8.3 g / l.

【0027】洗濯実験は、以下の条件下でTerg−0
−tometer中で実施した。 温度:25℃ 時間:10分 水 :3°DH
The washing experiment was carried out under the following conditions: Terg-0
Carried out in a -meter. Temperature: 25 ° C Time: 10 minutes Water: 3 ° DH

【0028】洗濯後の脂肪酸残留量を、ソックスレー抽
出によりに測定し残留脂肪酸量として表3に示した。洗
濯前の被洗布中脂肪酸含量は2.87%であった。
The residual amount of fatty acid after washing was measured by Soxhlet extraction and shown in Table 3 as the amount of residual fatty acid. The fatty acid content in the cloth to be washed before washing was 2.87%.

【0029】表1、2、3の結果より、本発明に係る糖
エステル系界面活性剤とアニオン界面活性剤を組み合わ
せた洗浄剤は、互いの相乗効果により起泡力、洗浄力の
増大することが確認された。
From the results of Tables 1, 2, and 3, the detergents according to the present invention in which the sugar ester-based surfactant and the anionic surfactant are combined are capable of increasing foaming power and detergency due to their synergistic effects. Was confirmed.

【0030】[0030]

【表−1】 [Table-1]

【0031】[0031]

【表−2】 [Table-2]

【0032】[0032]

【表−3】 [Table-3]

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】(A)炭素数6〜22の脂肪酸とジヘキソ
ースからなる二糖類、炭素数4〜6の糖アルコールから
選ばれた糖類からなる糖エステル系界面活性剤の1種又
は2種以上と、(B)−COO、−OSO 又は−
SO 基をもつアニオン界面活性剤から選ばれる1種
又は2種以上を,(A)/(B)成分比が1/5〜5/
1(w/w)でかつ、(A)+(B)が5〜50重量%
の範囲で含有してなることを特徴とする洗浄剤。
1. One or more kinds of (A) a disaccharide composed of a fatty acid having 6 to 22 carbon atoms and a dihexose, and a sugar ester surfactant composed of a sugar selected from a sugar alcohol having 4 to 6 carbon atoms. If, (B) -COO -, -OSO 3 - or -
One or two or more selected from anionic surfactants having SO 3 groups, the ratio of (A) / (B) components is 1/5 to 5 /
1 (w / w) and 5 to 50% by weight of (A) + (B)
A cleaning agent characterized by being contained in the range of.
JP30696693A 1993-11-02 1993-11-02 Detergent Pending JPH07126689A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP30696693A JPH07126689A (en) 1993-11-02 1993-11-02 Detergent

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP30696693A JPH07126689A (en) 1993-11-02 1993-11-02 Detergent

Publications (1)

Publication Number Publication Date
JPH07126689A true JPH07126689A (en) 1995-05-16

Family

ID=17963414

Family Applications (1)

Application Number Title Priority Date Filing Date
JP30696693A Pending JPH07126689A (en) 1993-11-02 1993-11-02 Detergent

Country Status (1)

Country Link
JP (1) JPH07126689A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6169060B1 (en) 1998-12-11 2001-01-02 Johnson & Johnson Kabushiki Kaisha Cleanser composition including a mixture of anionic, nonionic, and amphoteric surfactants

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6169060B1 (en) 1998-12-11 2001-01-02 Johnson & Johnson Kabushiki Kaisha Cleanser composition including a mixture of anionic, nonionic, and amphoteric surfactants

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