JPS63161083A - Liquid detergent composition - Google Patents

Liquid detergent composition

Info

Publication number
JPS63161083A
JPS63161083A JP31043086A JP31043086A JPS63161083A JP S63161083 A JPS63161083 A JP S63161083A JP 31043086 A JP31043086 A JP 31043086A JP 31043086 A JP31043086 A JP 31043086A JP S63161083 A JPS63161083 A JP S63161083A
Authority
JP
Japan
Prior art keywords
group
carbon atoms
formula
weight
surfactants
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
JP31043086A
Other languages
Japanese (ja)
Other versions
JPH0715116B2 (en
Inventor
秀一 荻野
順子 小倉
一 廣田
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 JP61310430A priority Critical patent/JPH0715116B2/en
Publication of JPS63161083A publication Critical patent/JPS63161083A/en
Publication of JPH0715116B2 publication Critical patent/JPH0715116B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Landscapes

  • Detergent Compositions (AREA)

Abstract

(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。
(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.

Description

【発明の詳細な説明】 〔産業上の利用分野〕 本発明は、液体洗浄剤組成物に関し、更に詳しくは、強
電解性の界面活性剤とヒドロキシプロピルメチルセルロ
ースを含有する、優れた安定性を有し、かつ泡にクリー
ミーさ、なめらかさを付与し、泡のもちもよく、すすぎ
後の残溜窓(べたつき)を抑えた洗浄剤組成物に関する
DETAILED DESCRIPTION OF THE INVENTION [Industrial Application Field] The present invention relates to a liquid detergent composition, and more particularly, to a liquid cleaning composition containing a strong electrolytic surfactant and hydroxypropyl methyl cellulose and having excellent stability. The present invention also relates to a cleaning composition which imparts creaminess and smoothness to the foam, has good foam retention, and suppresses residual residue (stickiness) after rinsing.

〔従来の技術およびその問題点〕[Conventional technology and its problems]

従来、液体洗浄剤の泡の改質剤としては、脂肪酸のアル
カノールアミドやモノグリセライド、各種イオン性ポリ
マーが用いられていた。しかし、これらは多量に配合し
ないと効果がなく、また、十分に効果を奏する程度の量
を配合すると洗浄後の感触が重い、あるいは、べたつく
などの問題があった。
Conventionally, fatty acid alkanolamides, monoglycerides, and various ionic polymers have been used as foam modifiers for liquid detergents. However, they are not effective unless they are blended in large amounts, and if they are blended in amounts that are sufficient to produce a sufficient effect, there are problems such as a heavy or sticky feel after washing.

又、ポリエチレンオキシド等の非イオン性ポリマーは、
強電解質性の界面活性剤中で低温安定性が慈くなる等の
問題があった。
In addition, nonionic polymers such as polyethylene oxide,
There were problems such as poor low temperature stability among strong electrolytic surfactants.

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

本発明者らは、この様な従来の問題を改善し、クリーミ
ーでもちのよい泡質にし、しかも洗浄後のべたつきを抑
え、特に、毛髪に関しては洗髪中の髪のからみをなくシ
、すすぎ後のなめらかさを与えることを目的に鋭意検討
した。そしてその結果、特定のヒドロキシプロピルメチ
ルセルロースは強電解質界面活性剤の存在下でも低温安
定性に優れ、しかも少量で十分な泡質が得られることを
見出した。すなわち、ヒドロキシプロピルメチルセルロ
ースを配合することによシきめの細がくすべりの良い泡
が得られ、かつ、すすぎ後の感触がなめらかな液体洗浄
剤組成物が得られることを見出した。
The present inventors have solved these conventional problems by creating a creamy and long-lasting foam that also suppresses stickiness after washing.In particular, with regard to hair, it eliminates tangles during hair washing and improves the quality of the foam after rinsing. We worked hard to give it a smooth feel. As a result, they found that a specific hydroxypropyl methylcellulose has excellent low-temperature stability even in the presence of a strong electrolyte surfactant, and that sufficient foam quality can be obtained with a small amount. That is, it has been found that by blending hydroxypropyl methylcellulose, a liquid detergent composition that has a fine texture and smooth foam and a smooth feel after rinsing can be obtained.

すなわち、本発明は次の成分(A)及び(B)(A)次
の式(I)、 (式中、分子末端及びRは水素原子、メチル基又はヒド
ロキシプロピル基のいずれかである)で表わされる構造
単位を有し、メトキシ基の含有率が25〜35重量%、
ヒドロキシプロポキシ基の含有率が5〜15%であシ、
その2重量チ水溶液の20℃での粘度が50〜2ooo
センチポアズであるヒドロキシプロピルメチルセルロー
ス 0.1〜2重量%、 (B)  陽イオン性界面活性剤、陰イオン性界面活性
剤及び両性界面活性剤よシなる群から選ばれる界面活性
剤の一種又は二種以上 2〜50重量% を必須成分として含有する液体洗浄剤組成物を提供する
ものである。
That is, the present invention comprises the following components (A) and (B) (A) of the following formula (I), (wherein the molecular terminal and R are either a hydrogen atom, a methyl group or a hydroxypropyl group) having the structural unit represented by the formula, and having a methoxy group content of 25 to 35% by weight,
The content of hydroxypropoxy groups is 5 to 15%,
The viscosity of the 2 weight aqueous solution at 20°C is 50 to 2ooo
0.1 to 2% by weight of hydroxypropyl methylcellulose, which is centipoise; (B) one or two surfactants selected from the group consisting of cationic surfactants, anionic surfactants, and amphoteric surfactants; The present invention provides a liquid detergent composition containing 2 to 50% by weight of the above as an essential component.

本発明の(A)成分として用いられるヒドロキシプロピ
ルメチルセルロースは前記一般式(I)で表わされる構
造単位を有するものであシ、好ましくは、平均分子量が
2QOOO〜7QOOOのものである。
Hydroxypropyl methyl cellulose used as component (A) of the present invention has a structural unit represented by the above general formula (I), and preferably has an average molecular weight of 2QOOO to 7QOOO.

このヒドロキシプロピルメチルセルロースは公知の方法
で合成でき、また市販品として入手することもできる。
This hydroxypropyl methylcellulose can be synthesized by a known method, and can also be obtained as a commercially available product.

このヒドロキシプロピルメチルセルロースは2重量%(
以下単にチで示す)水溶液とし、BM粘度計を用いて2
0℃、30回転/分で測定したときの粘度が50〜40
00センチポア、<(CPS)のものである。ちなみに
50CPSのものは平均分子量約2QOOO12000
CPSのものは平均分子量約7QOOOである。500
PS以下のものでは十分な泡改質効果がみられず、zo
o。
This hydroxypropyl methylcellulose is 2% by weight (
(hereinafter simply indicated as H) as an aqueous solution, and using a BM viscometer,
Viscosity is 50-40 when measured at 0°C and 30 revolutions/min.
00 centipore, <(CPS). By the way, the average molecular weight of 50CPS is about 2QOOO12000
CPS has an average molecular weight of about 7QOOO. 500
If the foam is less than PS, a sufficient foam modification effect cannot be seen, and zo
o.

028以上のものでは溶解性不良となる。If it is more than 028, the solubility will be poor.

また当該ヒドロキシプロピルメチルセルロースはセルロ
ースの水酸基の1部がメトキシ基もしくはヒドロキシプ
ロポキシ基に置換されたものであシ、メトキシ基の含有
率はヒドロキシプロピルメチルセルロース中25〜35
%、好マシくハ27〜32%ヒドロキシプロポキシ基の
含有率は5〜15%、好ましくは7〜13%である。こ
れらの置換度は約1.5〜2.0、すなわちグルコース
1単位に含まれる3個の水酸基の内、約1.5〜2.0
個が置換されたものである。この範囲外のヒドロキシプ
ロピルメチルセルロースは20℃、2%水溶液の粘度が
50〜z000であっても溶解性、低温安定性が不良と
なる。
In addition, the hydroxypropyl methylcellulose is one in which a part of the hydroxyl groups of cellulose is substituted with a methoxy group or a hydroxypropoxy group, and the content of methoxy groups is 25 to 35% in the hydroxypropyl methylcellulose.
%, preferably 27-32% The content of hydroxypropoxy groups is 5-15%, preferably 7-13%. The degree of substitution is approximately 1.5 to 2.0, that is, approximately 1.5 to 2.0 among the three hydroxyl groups contained in one unit of glucose.
are replaced. Hydroxypropyl methylcellulose outside this range has poor solubility and low-temperature stability even if the viscosity of a 2% aqueous solution at 20° C. is 50 to z000.

上記ヒドロキシプロピルメチルセルロースの内低温安定
性、泡改質効果の相方の点で最も適するものとしてメト
キシ基含有率28〜30%、ヒドロキシプロポキシ基含
有率7〜12%、20℃、2%水溶液の粘度が約400
(平均分子量約4QOOO)のヒドロキシプロピルメチ
ルセルロース(メトローズ60 S H,信越化学)が
挙げられる。
Among the above-mentioned hydroxypropyl methylcellulose, the most suitable one in terms of low-temperature stability and foam-modifying effect is a methoxy group content of 28 to 30%, a hydroxypropoxy group content of 7 to 12%, and a viscosity of a 2% aqueous solution at 20°C. is about 400
Hydroxypropyl methyl cellulose (Metrose 60 S H, Shin-Etsu Chemical) with an average molecular weight of about 4QOOO is exemplified.

また、(B)成分の界面活性剤のうち、陰イオン性界面
活性剤としては、次のものが例示される。
Moreover, among the surfactants of component (B), the following are exemplified as anionic surfactants.

(I)平均炭素数10〜16のアルキル基を有する直鎖
又は分岐鎖アルキルベンゼンスルホン酸塩。
(I) A linear or branched alkylbenzene sulfonate having an alkyl group having an average carbon number of 10 to 16.

(2)平均炭素数10〜20の直鎖又は分岐鎖のアルキ
ル基又はアルケニル基を有し、1分子内に平均0.5〜
8モルのエチレンオキサイド、プロピレンオキサイド、
ブチレンオキサイド、エチレンオキサイドとプロピレン
オキサイドが0.1/9,9〜9.9 / 0.1の比
であるいはエチレンオキサイドとブチレンオキサイドが
0.1 / 9.9〜9、9 / 0.1の比で付加し
たアルキル又はアルケニルエーテル硫酸塩。
(2) Contains a linear or branched alkyl group or alkenyl group with an average of 10 to 20 carbon atoms, with an average of 0.5 to 20 carbon atoms per molecule.
8 moles of ethylene oxide, propylene oxide,
Butylene oxide, ethylene oxide and propylene oxide in a ratio of 0.1/9,9-9.9/0.1 or ethylene oxide and butylene oxide in a ratio of 0.1/9.9-9,9/0.1 Alkyl or alkenyl ether sulfate added in ratio.

(3)平均炭素数10〜20のアルキル基又はアルケニ
ル基を有するアルキル又はアルケニル硫酸塩。
(3) An alkyl or alkenyl sulfate having an alkyl group or alkenyl group having an average carbon number of 10 to 20.

(A)平均10〜20の炭素原子を1分子中に有するオ
レフィンスルホン酸塩。
(A) Olefin sulfonate having an average of 10 to 20 carbon atoms in one molecule.

(5)平均10〜20の炭素原子を1分子中に有するア
ルカンスルホン酸塩。
(5) Alkanesulfonate having an average of 10 to 20 carbon atoms in one molecule.

(6)平均10〜24の炭素原子を1分子中に有する飽
和又は不飽和脂肪酸塩。
(6) A saturated or unsaturated fatty acid salt having an average of 10 to 24 carbon atoms in one molecule.

(7)  平均炭素数10〜20のアルキル基又はアル
ケニル基を有し、1分子中に平均0.5〜8モルのエチ
レンオキサイド、プロピレンオキサイド、ブチレンオキ
サイド、エチレンオキサイドとプロピレンオキサイドが
0.1 / 9.9〜9.9 / 0.1の比であるい
はエチレンオキサイドとブチレンオキサイドが0.1 
/ 9.9〜9.9 / 0.1の比で付加したアルキ
ル又はアルケニルエーテルカルボン酸塩。
(7) It has an alkyl group or alkenyl group with an average carbon number of 10 to 20, and an average of 0.5 to 8 moles of ethylene oxide, propylene oxide, butylene oxide, ethylene oxide and propylene oxide in 0.1 / molecule per molecule. 9.9-9.9/0.1 ratio or ethylene oxide and butylene oxide 0.1
/9.9 to 9.9/0.1 alkyl or alkenyl ether carboxylate.

(8)下記の式で表されるα−スルホ脂肪酸塩又はエス
テル。
(8) α-sulfo fatty acid salt or ester represented by the following formula.

Ry−CHC(hY 03Z (式中Yは炭素数1〜3のアルキル基又は対イオン、2
は対イオンである。R7は炭素数10〜20のアルキル
基又はアルケニル基を表す。)(9)下記一般式で表さ
れるアミノ酸型界面活性剤。
Ry-CHC(hY 03Z (wherein Y is an alkyl group having 1 to 3 carbon atoms or a counter ion, 2
is the counterion. R7 represents an alkyl group or alkenyl group having 10 to 20 carbon atoms. ) (9) An amino acid type surfactant represented by the following general formula.

9 RIG (式中R8は炭素数8〜24のアルキル基又はアルケニ
ル基を、Rgは水素原子又は炭素数1〜2のアルキル基
を、RIGはアミノ酸残基を、Xはアルカリ金属又はア
ルカリ土類金属イオンを示す。) (式中、R8、R9及びXは前記したt味を有し、nl
は1〜5の整数を示す。) C式中、Rs及びXは前記した意味を有し、mlは1〜
8の整数を示す。) R11RIO (式中、R8、RIo 及びXは前記した意味を有し、
R11は水素原子、炭素数1〜2のアルキル基又はヒド
ロキシアルキル基を示す。)9 RIO (式中、R9、RIO及びXは前記した意味を有し、R
12は炭素数6〜28のβ−ヒドロキシアルキル基又は
β−ヒドロキシアルケニル基を示す。) RIG (式中、RIOs R+2及びXは前記した意味を有す
る。) (式中、R13、R14、R15は炭素数7〜23の炭
化水素基を、tは1もしくは2であり、Xは前記した意
味を有する) (I0)  リン酸エステル系界面活性剤(I)アルキ
ル(又はアルケニル)酸性リン酸エステル (R80)H2−P−+OH)H2 (式中、R8は前記した意味を有し、H2及び鞠は、n
3+膓=3、n2=1〜2である数を示す。)(n) 
 アルキル(又はアルケニル)リン酸エステル OR。
9 RIG (wherein R8 is an alkyl group or alkenyl group having 8 to 24 carbon atoms, Rg is a hydrogen atom or an alkyl group having 1 to 2 carbon atoms, RIG is an amino acid residue, and X is an alkali metal or alkaline earth (Indicates a metal ion.) (In the formula, R8, R9 and X have the above-mentioned taste, and nl
represents an integer from 1 to 5. ) In formula C, Rs and X have the meanings described above, and ml is 1 to
Indicates an integer of 8. ) R11RIO (wherein R8, RIo and X have the above meanings,
R11 represents a hydrogen atom, an alkyl group having 1 to 2 carbon atoms, or a hydroxyalkyl group. )9 RIO (wherein R9, RIO and X have the meanings described above, R
12 represents a β-hydroxyalkyl group or a β-hydroxyalkenyl group having 6 to 28 carbon atoms. ) RIG (In the formula, RIOs R+2 and (I0) Phosphate surfactant (I) Alkyl (or alkenyl) acidic phosphate ester (R80) H2-P-+OH)H2 (wherein R8 has the above meaning, H2 and Mari are n
Indicates a number where 3+膓=3 and n2=1 to 2. )(n)
Alkyl (or alkenyl) phosphate ester OR.

Rs O−P −ORs (式中、R8は前記した意味を有する。)(iiD  
アルキル(又はアルケニル)リン酸エステル塩 (Rao )R3−P→OM )H3 (式中、R8は前記した意味を有し、Mはナトリウム、
カリウム、カルシウムを、R3及び簡は、n3+膓=3
、n3=1〜3である数を示も)また、両性イオン界面
活性剤としては、次のものが例示される。
Rs OP -ORs (wherein, R8 has the meaning described above) (iiD
Alkyl (or alkenyl) phosphate ester salt (Rao)R3-P→OM)H3 (wherein R8 has the above meaning, M is sodium,
Potassium, calcium, R3 and simple, n3 + 膓 = 3
, n3=1 to 3) Examples of the zwitterionic surfactants include the following.

(U)スルホン酸型両性界面活性剤 (I)  RBCONH−R13−N” −Rts −
SO3−(式中、R11は前記した、意味を有し、R1
3は炭素数1〜4のアルキレン基を、R14は炭素数1
〜5のアルキル基を、R15は炭素数1〜4のアルキレ
ン基又はヒドロキシアルキレン基を示す。) (I)  R@ −N” −Rts −803−(式中
、Rs及びR15は前記した意味を有し、Rla 、 
R1?はそれぞれ炭素数8〜24又は炭素数1〜5のア
ルキル基又はアルケニル基を示す。) (C2H40)n4H C式中、R11及びR15は前記した意味を有し、H4
は1〜20の整数を示す。) (I2)次の一般式で示されるベタイン型両性界面活性
剤 (I)  Rls −N” −R2O−COO−1式中
、R18は炭素数8〜24のアルキル基、アルケニル基
、β−ヒドロキシアルキル基又はβ−ヒドロキシアルケ
ニル基を、R19は炭素数1〜4のアルキル基を、Rg
oは炭素数1〜6のアルキレン基又はヒドロキシアルキ
レン基を示す。) ■ (C,H40)n4H 1式中、RIJl、R40及びH4は前記した意味を有
する。) (lti)  Rts −N+−Rzo −COO−(
式中、Rlg及びR20は前記した意味を有し、lhl
はカルボキシアルキル基又はヒドロキシアルキル基を示
す。) (I3)次の式で表されるアルキルアミンオキサイド。
(U) Sulfonic acid type amphoteric surfactant (I) RBCONH-R13-N"-Rts-
SO3- (wherein R11 has the meaning described above, R1
3 is an alkylene group having 1 to 4 carbon atoms, and R14 is an alkylene group having 1 to 4 carbon atoms.
-5 alkyl group, and R15 represents an alkylene group or hydroxyalkylene group having 1 to 4 carbon atoms. ) (I) R@-N"-Rts-803- (wherein Rs and R15 have the above-mentioned meanings, Rla,
R1? each represents an alkyl group or an alkenyl group having 8 to 24 carbon atoms or 1 to 5 carbon atoms. ) (C2H40)n4H In the formula, R11 and R15 have the above meanings, and H4
represents an integer from 1 to 20. ) (I2) Betaine type amphoteric surfactant represented by the following general formula (I) Rls -N'' -R2O-COO-1 In the formula, R18 is an alkyl group having 8 to 24 carbon atoms, an alkenyl group, β-hydroxy R19 is an alkyl group or β-hydroxyalkenyl group, R19 is an alkyl group having 1 to 4 carbon atoms, Rg
o represents an alkylene group or a hydroxyalkylene group having 1 to 6 carbon atoms. ) (C,H40)n4H 1 In the formula, RIJl, R40 and H4 have the above-mentioned meanings. ) (lti) Rts -N+-Rzo -COO-(
In the formula, Rlg and R20 have the meanings described above, and lhl
represents a carboxyalkyl group or a hydroxyalkyl group. ) (I3) Alkylamine oxide represented by the following formula.

Rts R? −N−4Q 1式中、R7は前記した意味を有し、R23、R24は
それぞれ炭素数1〜3のアルキル基を示す。)更に、カ
チオン性界面活性剤としては、次のものが例示される。
Rts R? -N-4Q In formula 1, R7 has the meaning described above, and R23 and R24 each represent an alkyl group having 1 to 3 carbon atoms. ) Furthermore, the following are exemplified as cationic surfactants.

(I4)次の式で示されるカチオン界面活性剤。(I4) A cationic surfactant represented by the following formula.

C式中、R28% Ro、R27、R28のうち少なく
とも1個は炭素数8〜24のアルキル基又はアルケニル
基を、他は炭素数1〜5のアルキル基を示し、X゛はハ
ロゲン原子を示す。)(式中、Rzs 、R26、R2
γ及びX″は前記した意味を有する。) (式中、’Rzs、R16、X’及びR4は前記した意
味を有し、R28は炭素数2〜3のアルキレン基を示す
。) 叙上の洗浄剤基剤である界面活性剤のうち、特に好まし
いものは(2)のポリオキシエチレンアルキル硫酸エス
テル塩(平均付加モル数2〜4)と、(9) &Iの2
級アミドアミノ酸型界面活性剤、特に、そのナトリウム
塩等そのアルカリ金属塩である。
In formula C, at least one of R28% Ro, R27, and R28 represents an alkyl group or alkenyl group having 8 to 24 carbon atoms, the others represent an alkyl group having 1 to 5 carbon atoms, and X'' represents a halogen atom. . ) (wherein, Rzs, R26, R2
γ and X'' have the above meanings.) (In the formula, 'Rzs, R16, X' and R4 have the above meanings, and R28 represents an alkylene group having 2 to 3 carbon atoms. Among the surfactants that are the detergent base, particularly preferred are (2) polyoxyethylene alkyl sulfate salt (average number of added moles of 2 to 4), and (9) &I 2
amide amino acid type surfactants, particularly their alkali metal salts such as their sodium salts.

すなわち、これらアニオン界面活性剤のアルカリ金属塩
、特にそのナトリウム塩は液体洗浄剤基剤として最も好
ましいものの一つであるが、強電解質であるため、ボリ
エデレンオキシド等の非イオン性ポリマーを泡の改質剤
として加えても塩析されてしまい、泡質改質効果は得ら
れず、安定に配合することはできなかった。しかしなが
ら、本発明の(A)成分であるヒドロキシプロピルメチ
ルセルロースは、アニオン界面活性剤のアルカノールア
ミン塩のごとき弱電解質を基剤とする液体洗浄剤はもち
ろん、上記したような強電解質を基剤とする液体洗浄剤
中にも配合することができ、優れた泡改質効果を奏する
In other words, the alkali metal salts of these anionic surfactants, especially their sodium salts, are among the most preferred as liquid detergent bases, but because they are strong electrolytes, they do not allow foaming of nonionic polymers such as polyederene oxide. Even if it was added as a modifier, it would salt out, and no foam-modifying effect could be obtained, making it impossible to mix stably. However, hydroxypropyl methylcellulose, which is the component (A) of the present invention, can be used not only in liquid detergents based on weak electrolytes such as alkanolamine salts of anionic surfactants, but also in liquid detergents based on strong electrolytes such as those described above. It can also be incorporated into liquid detergents and has an excellent foam-modifying effect.

本発明の洗浄剤組成物は、常法に従い、前記(A)成分
を0.1〜2重景%(以下単にチで示す)、(B)成分
を2〜50%配合することによシ調製される。
The cleaning composition of the present invention can be prepared by blending the component (A) in an amount of 0.1 to 2% (hereinafter simply referred to as "C") and the component (B) in an amount of 2 to 50% according to a conventional method. prepared.

本発明の洗浄剤組成物には、上記の必須成分の他に、公
知の洗浄剤組成物の配合成分として用いられるプロピレ
ングリコール、グリセリン、尿素等の溶解剤、エタノー
ル、無機塩、高級アルコール、ポリアクリル酸等の粘度
調整剤、その他香料、色素、紫外線吸収剤、酸化防止剤
、抗フケ剤、殺菌剤、防腐剤等を配合することもできる
In addition to the above-mentioned essential ingredients, the cleaning composition of the present invention contains solubilizers such as propylene glycol, glycerin, and urea, which are used as ingredients in known cleaning compositions, ethanol, inorganic salts, higher alcohols, and polypropylene. A viscosity modifier such as acrylic acid, other fragrances, pigments, ultraviolet absorbers, antioxidants, anti-dandruff agents, bactericidal agents, preservatives, etc. can also be blended.

〔発明の効果〕〔Effect of the invention〕

本発明の洗浄剤組成物は、強電解質による優れた洗浄性
と、ヒドロキシプロピルメチルセルロースによる優れた
泡特性を併有するものである。したがって、特にシャン
プー、皮膚洗浄剤、食器洗浄剤等として有利に利用する
ことができる。
The cleaning composition of the present invention has both excellent cleaning properties due to the strong electrolyte and excellent foaming properties due to the hydroxypropyl methylcellulose. Therefore, it can be particularly advantageously used as shampoo, skin cleansing agent, dishwashing agent, etc.

〔実施例〕〔Example〕

以下に実施例を挙げ、本発明を更に詳しく説明する。な
お以下の実験において、液体洗浄剤を下記のとおり評価
した。また、成分の量はいずれも有効分の重it%で示
した。
The present invention will be explained in more detail with reference to Examples below. In addition, in the following experiment, the liquid cleaning agent was evaluated as follows. In addition, the amounts of the ingredients are all shown in weight it% of the effective content.

(I)溶解性、低温安定性: 常法によシ液体洗浄剤組成物を調製し、調製直後の液の
状態を下記基準で判定して「溶解性」として、また−5
℃に1日保存したときの状態を同様に判定して「低温安
定性」として示した。
(I) Solubility, low-temperature stability: A liquid detergent composition is prepared by a conventional method, and the state of the liquid immediately after preparation is judged according to the following criteria, and it is determined as "solubility" and -5.
The condition when stored at ℃ for 1 day was determined in the same manner and indicated as "low temperature stability".

O:透明均一。O: Transparent and uniform.

Δ :やや不透明、もしくは少量の沈殿あり。Δ: Slightly opaque or with a small amount of precipitate.

× :多量の沈殿もしくは相分離を認める。×: A large amount of precipitation or phase separation was observed.

(2)泡のすべり、クリーミーさ、すすぎ後のべたつき
: 30?の入毛を40℃の水で湿らせ、202の水を含ま
せる。次いで上記の液体洗浄剤組成物1?使用して洗浄
し、洗浄中の泡のすベシ、クリーミーさおよびすすぎ後
のべたつきのなさを対照シャンプー(それぞれの実験で
ヒドロキシプロピルメチルセルロースを含まないもの)
と比較し、官能評価した。
(2) Smoothness of foam, creaminess, stickiness after rinsing: 30? Moisten the hair with 40℃ water and add 202℃ of water. Next, the above liquid cleaning composition 1? A control shampoo (without hydroxypropyl methylcellulose in each experiment) was used to cleanse and evaluate the sudsiness, creaminess, and non-stickiness after rinsing.
A sensory evaluation was conducted in comparison with

評価   内 容 O:対照シャンプーより明らかに優れる。Evaluation details O: Clearly superior to the control shampoo.

Δ :対照シャンプーよりやや優れる。Δ: Slightly better than the control shampoo.

× :対照シャンプーと同じ。×: Same as control shampoo.

実施例1 第1表に示す液体洗浄剤組成物を常法に従って調製し、
その溶解性及び低温安定性を評価した。
Example 1 A liquid cleaning composition shown in Table 1 was prepared according to a conventional method,
Its solubility and low temperature stability were evaluated.

こ、の結果も同表に示す。なお、第1表の組成中、ヒド
ロキシプロピルメチル・セルロースは、スべてその2%
水浴液の20℃における粘度が約400(平均分子量約
4QOOO)のものである。
The results of this are also shown in the same table. In addition, in the composition of Table 1, hydroxypropyl methyl cellulose accounts for 2% of the total.
The viscosity of the water bath liquid at 20°C is about 400 (average molecular weight about 4QOOO).

(I)ミラノールC2Mコンク(ミラノール社製;(9
) Gv)式においてR13CO=ヤシ脂肪酸残基、t
=1、X = NaOもの) (2)メトキシ基29%、ヒドロキシプロポキシ基8゜
5%(3)      28%、          
  60係(A)   l  21.5%、     
       8 %(5)   1 29%(ヒドロ
キシプロポキシ基不含)(6)セロポンド45000 
A (B P社);25℃、10%水溶液の粘度500
0PS(平均分子量約2,700 ) (7)信越I(PC,EFG(信越化学社):25℃、
1%水溶液の粘度1500(平均分子量約2.000) 実施例2 種々の粘度のヒドロキシプロピルメチルセルロースを用
いて液体洗浄剤組成物(シャンプー)を調製し、その溶
解性及び泡のすベシを評価した。
(I) Milanor C2M Conc (manufactured by Milanor); (9
) Gv) In the formula, R13CO=coconut fatty acid residue, t
= 1, X = NaO) (2) methoxy group 29%, hydroxypropoxy group 8°5% (3) 28%,
Section 60 (A) l 21.5%,
8% (5) 1 29% (Hydroxypropoxy group free) (6) Ceropond 45,000
A (B P Company); 25°C, viscosity of 10% aqueous solution 500
0PS (average molecular weight approximately 2,700) (7) Shin-Etsu I (PC, EFG (Shin-Etsu Chemical): 25°C,
Viscosity of 1% aqueous solution: 1500 (average molecular weight approximately 2.000) Example 2 Liquid detergent compositions (shampoos) were prepared using hydroxypropyl methylcellulose of various viscosities, and their solubility and foam strength were evaluated. .

この結果を第2表に示す。なお、用いたヒドロキシプロ
ピルメチルセルロースのメトキシ基含有率及びヒドロキ
シプロポキシ含有率はいずれもそれぞれ29%及び9.
5%である。
The results are shown in Table 2. The methoxy group content and hydroxypropoxy content of the hydroxypropyl methylcellulose used were 29% and 9.9%, respectively.
It is 5%.

(組成) ポリオキシエチレン(3)ラウリル硫酸ナトリウム 1
5チヒドロキシプロビルメチルセルロース(第2表) 
 0.5ラウリン酸ジエタノールアミド   3イオン
交換水           残部第2表 比較品5     5(aooo)       OX
16   to(Ia00o)     Ox本発明品
3   50(2QOOO)       OOl  
4 100(2へ000 )     ○  Ol5 
200 (33ooo)     ○  C16400
(AQOOO)     O○−7600(5QOOO
)     OOl8 800(5へ000)    
 ○  0I91,500(6へ000 )     
OOl10 2.000  (’7QOOO)    
  OO比較品7  4,000  (80,000)
        X    X米20℃、2%水溶液の
粘度(CPS)および平均分子it(カッコ内)。
(Composition) Polyoxyethylene (3) Sodium lauryl sulfate 1
5-hydroxypropyl methylcellulose (Table 2)
0.5 Lauric acid diethanolamide 3 Ion exchange water Remainder Table 2 Comparative product 5 5 (aooo) OX
16 to (Ia00o) Ox invention product 3 50 (2QOOO) OOl
4 100 (000 to 2) ○ Ol5
200 (33ooo) ○ C16400
(AQOOO) O○-7600 (5QOOO
) OOl8 800 (000 to 5)
○ 0I91,500 (000 to 6)
OOl10 2.000 ('7QOOO)
OO comparison product 7 4,000 (80,000)
Viscosity (CPS) and average molecular weight (in parentheses) of a 2% aqueous solution at 20°C.

実施例3 第3表に示す組成の液体洗浄剤組成物(シャンプー)を
調製し、その性能を官能的に評価した。
Example 3 A liquid detergent composition (shampoo) having the composition shown in Table 3 was prepared, and its performance was sensory evaluated.

この結果も同表中に示す。The results are also shown in the same table.

第3表 来ヒドロキシプロピルメチルセルロース20℃における
2%水溶液の粘度は4000PS(平均分子量4QOO
O)、メトキシ基含有率28〜30%、ヒドロキシプロ
ポキシ基含有率7〜12チである。
The viscosity of a 2% aqueous solution of hydroxypropyl methylcellulose at 20°C is 4000PS (average molecular weight 4QOO
O), the methoxy group content is 28 to 30%, and the hydroxypropoxy group content is 7 to 12%.

以上that's all

Claims (1)

【特許請求の範囲】 1、次の成分(A)及び(B) (A)次の式( I )、 ▲数式、化学式、表等があります▼( I ) (式中、分子末端及びRは水素原子、メチル基又はヒド
ロキシプロピル基のいずれかである) で表わされる構造単位を有し、メトキシ基の含有率が2
5〜35重量%、ヒドロキシプロポキシ基の含有率が5
〜15%であり、その2重量%水溶液の20℃での粘度
が50〜 2,000センチポアズであるヒドロキシプロピルメチ
ルセルロース 0.1〜2重量%、 (B)陽イオン性界面活性剤、陰イオン性界面活性剤及
び両性界面活性剤よりなる群から選ばれる界面活性剤の
一種又は二種以上 2〜50重量% を必須成分として含有する液体洗浄剤組成物。
[Claims] 1. The following components (A) and (B) (A) The following formula (I), ▲There are mathematical formulas, chemical formulas, tables, etc.▼(I) (In the formula, the molecule terminal and R are hydrogen atom, methyl group or hydroxypropyl group), and the content of methoxy groups is 2
5 to 35% by weight, the content of hydroxypropoxy groups is 5
0.1 to 2% by weight of hydroxypropyl methylcellulose whose 2% by weight aqueous solution has a viscosity of 50 to 2,000 centipoise at 20°C, (B) a cationic surfactant, an anionic surfactant; A liquid cleaning composition containing as an essential component 2 to 50% by weight of one or more surfactants selected from the group consisting of surfactants and amphoteric surfactants.
JP61310430A 1986-12-24 1986-12-24 Liquid detergent composition Expired - Fee Related JPH0715116B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP61310430A JPH0715116B2 (en) 1986-12-24 1986-12-24 Liquid detergent composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP61310430A JPH0715116B2 (en) 1986-12-24 1986-12-24 Liquid detergent composition

Publications (2)

Publication Number Publication Date
JPS63161083A true JPS63161083A (en) 1988-07-04
JPH0715116B2 JPH0715116B2 (en) 1995-02-22

Family

ID=18005148

Family Applications (1)

Application Number Title Priority Date Filing Date
JP61310430A Expired - Fee Related JPH0715116B2 (en) 1986-12-24 1986-12-24 Liquid detergent composition

Country Status (1)

Country Link
JP (1) JPH0715116B2 (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5783200A (en) * 1997-01-21 1998-07-21 The Procter & Gamble Company Personal cleansing compositions
US5785979A (en) * 1997-01-21 1998-07-28 The Procter & Gamble Company Personal cleansing compositions
EP1422288A1 (en) * 2002-11-21 2004-05-26 L'oreal Liquid cleaning composition containing soaps and synthetic surfactants; its use for cleaning human keratinous materials
JP2011510149A (en) * 2008-01-22 2011-03-31 ザ プロクター アンド ギャンブル カンパニー Liquid detergent composition
US8512480B2 (en) 2008-01-22 2013-08-20 The Procter & Gamble Company Liquid detergent composition comprising a hydrophobically modified cellulosic polymer

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2008508201A (en) * 2004-07-27 2008-03-21 ユニリーバー・ナームローゼ・ベンノートシヤープ Hair care composition

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5892453A (en) * 1981-11-12 1983-06-01 ジヨセフ・ア−ル・エアリツチ Foam forming composition using multipurpose surface active agent base

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5892453A (en) * 1981-11-12 1983-06-01 ジヨセフ・ア−ル・エアリツチ Foam forming composition using multipurpose surface active agent base

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5783200A (en) * 1997-01-21 1998-07-21 The Procter & Gamble Company Personal cleansing compositions
US5785979A (en) * 1997-01-21 1998-07-28 The Procter & Gamble Company Personal cleansing compositions
EP1422288A1 (en) * 2002-11-21 2004-05-26 L'oreal Liquid cleaning composition containing soaps and synthetic surfactants; its use for cleaning human keratinous materials
FR2847465A1 (en) * 2002-11-21 2004-05-28 Oreal LIQUID CLEANING COMPOSITION BASED ON SOAP AND SYNTHETIC SURFACTANTS; USES FOR CLEANING HUMAN KERATINIC MATERIALS
JP2011510149A (en) * 2008-01-22 2011-03-31 ザ プロクター アンド ギャンブル カンパニー Liquid detergent composition
US8512480B2 (en) 2008-01-22 2013-08-20 The Procter & Gamble Company Liquid detergent composition comprising a hydrophobically modified cellulosic polymer

Also Published As

Publication number Publication date
JPH0715116B2 (en) 1995-02-22

Similar Documents

Publication Publication Date Title
JP2964226B2 (en) Detergent composition
US4556510A (en) Transparent liquid shower soap
JP5041894B2 (en) Cleaning composition
EP0133345A1 (en) Opaque liquid hand soap
JP2004143072A (en) Cleaner composition
JPH04108724A (en) Detergent composition
JPS62138594A (en) Detergent composition
JPS63161083A (en) Liquid detergent composition
JPH0597633A (en) Detergent composition
JPH10203939A (en) Hair detergent composition
JP2761799B2 (en) Washing soap
JP4666343B2 (en) Mixture of acyl taurine salts and detergent composition containing the same
JPH0433999A (en) Low irritative cleanser composition
WO2022127421A1 (en) Cleaning composition
JPS6225197A (en) Liquid detergent composition
JPH035414A (en) Cleaning composition and its production
JPH09165319A (en) Transparent gel shampoo composition
JP3526314B2 (en) Shampoo composition
JPS6267011A (en) Hair rinse composition
CN116098821B (en) Cleaning composition containing surfactant system and application thereof
JP6017927B2 (en) Transparent hair cleanser
JPH01165512A (en) Detergent composition
JPS6330599A (en) Liquid detergent composition
JPH04164016A (en) Cleaning agent composition
JP2010037228A (en) Hair detergent composition

Legal Events

Date Code Title Description
LAPS Cancellation because of no payment of annual fees