JPH01242697A - Liquid cleanser composition - Google Patents

Liquid cleanser composition

Info

Publication number
JPH01242697A
JPH01242697A JP6892388A JP6892388A JPH01242697A JP H01242697 A JPH01242697 A JP H01242697A JP 6892388 A JP6892388 A JP 6892388A JP 6892388 A JP6892388 A JP 6892388A JP H01242697 A JPH01242697 A JP H01242697A
Authority
JP
Japan
Prior art keywords
weight
water
fatty acid
salt
partially crosslinked
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
JP6892388A
Other languages
Japanese (ja)
Other versions
JPH0524197B2 (en
Inventor
Hideji Tagata
秀次 田方
Atsuhiko Kaji
梶 敦彦
Masanori Takemura
政典 竹村
Katsuhiko Deguchi
勝彦 出口
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 JP6892388A priority Critical patent/JPH01242697A/en
Publication of JPH01242697A publication Critical patent/JPH01242697A/en
Publication of JPH0524197B2 publication Critical patent/JPH0524197B2/ja
Granted 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
    • C11D3/16Organic compounds
    • C11D3/37Polymers
    • C11D3/3746Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • C11D3/3757(Co)polymerised carboxylic acids, -anhydrides, -esters in solid and liquid compositions
    • C11D3/3765(Co)polymerised carboxylic acids, -anhydrides, -esters in solid and liquid compositions in liquid compositions

Landscapes

  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Wood Science & Technology (AREA)
  • Organic Chemistry (AREA)
  • Detergent Compositions (AREA)

Abstract

PURPOSE:To obtain the title compsn. which has excellent storage stability and does not cause toilet seat cracking, by incorporating a partially crosslinked polyacrylic acid, an anionic surfactant, a fatty acid (salt) and an alkanolamide each of particular type as essential components with the balance being a water- insoluble abrasive material and water. CONSTITUTION:0.1-1.0wt.% (hereinafter simply %) partially crosslinked polyacrylic acid having an average degree of polymn. of 10<3>-10<5> and a Brookfield yield value in 0.3wt.% aq. soln. of 100g/sec.cm or higher, 0.1-5.0wt.% at least one anionic surfactant contg. a sulfate or sulfonate but not contg. an oxyalkyl chain (e.g., alkanolamine salt or alkali metal salt of an alkylbenzensulfonate, etc.), 0.05-2.0% 10-22C fatty acid or alkali (alkaline earth) metal salt or alkanolamine salt thereof and 0.1-5.0% 10-22C fatty acid alkanolamide are incorporated as essential components. Further, 5-55% at least one water-insoluble abrasive material (e.g., silica, zeolite, etc.), and water are added thereto and blended together.

Description

【発明の詳細な説明】 〔産業上の利用分野〕 本発明は液体クレンザ−組成物に関するもの、更に詳し
くは便器、トイレの床の洗浄に適し、ABS樹脂製の便
座割れを起こさない、かつ長期の保存安定性に優れた水
洗トイレ用液体クレンザ−組成物に関する。
DETAILED DESCRIPTION OF THE INVENTION [Industrial Application Field] The present invention relates to a liquid cleanser composition, more specifically, suitable for cleaning toilet bowls and toilet floors, which does not cause cracking of toilet seats made of ABS resin, and which can be used for a long period of time. The present invention relates to a liquid cleanser composition for flush toilets that has excellent storage stability.

〔従来の技術及び発明が解決しようとする課題〕酸性ト
イレクリーナーの水洗トイレの自家浄化槽内微生物への
悪影響が懸念されることから、水洗トイレには中性液体
トイレクリーナーの使用が普及している。この中性トイ
レクリーナーには垂直面の洗い易さを向上させる為に部
分架橋ポリアクリル酸等の増粘剤を通常含有している。
[Prior art and problems to be solved by the invention] Due to concerns about the negative effects of acidic toilet cleaners on the microorganisms in private septic tanks of flush toilets, the use of neutral liquid toilet cleaners for flush toilets has become widespread. . These neutral toilet cleaners usually contain a thickening agent, such as partially crosslinked polyacrylic acid, to improve the ease of cleaning vertical surfaces.

この部分架橋ポリアクリル酸は電解質の存在下で凝集し
て低粘度、低降伏値になる傾向があるために通常併用さ
れる界面活性剤としては非イオン性界面活性剤、特にオ
キシエチレン基を含有する非イオン性界面活性剤が多い
(特開昭54−74810 、特開昭61−15759
1)。この種の中性トイレクリーナーは液が垂れにり<
、肌にマイルドであるという大きな特長を有するものの
、ABS樹脂製の便座をひび割れさせるという欠点があ
った。
This partially cross-linked polyacrylic acid tends to aggregate in the presence of electrolytes, resulting in low viscosity and low yield values, so the surfactant that is usually used in combination is a nonionic surfactant, especially one containing an oxyethylene group. There are many nonionic surfactants that
1). This type of neutral toilet cleaner does not drip liquid.
Although it has the great advantage of being mild to the skin, it has the drawback of causing cracks in ABS resin toilet seats.

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

本発明者等は便器、トイレの床の洗浄に適し、^BS樹
脂製の便座割れを起こさない水洗トイレ用液体洗浄剤組
成物を提供すべく鋭意検討した結果、部分架橋ポリアク
リル酸、サルフェート基またはスルホネート4を有し、
かつオキシエチレン基を含有しない陰イオン性界面活性
剤、脂肪酸、脂肪酸アルカノールアミドと水不溶性研磨
剤を特定量配合すれば良いことを見出し、本発明を完成
した。
The present inventors have conducted intensive studies to provide a liquid cleaning agent composition for flush toilets that is suitable for cleaning toilet bowls and toilet floors and does not cause cracking of toilet seats made of BS resin. or has sulfonate 4,
The present invention was completed based on the discovery that it is sufficient to blend specific amounts of an anionic surfactant containing no oxyethylene group, a fatty acid, a fatty acid alkanolamide, and a water-insoluble abrasive.

即ち、本発明は (al  平均重合度が103〜103で、0.3重量
%水溶液のブルックフィールド降伏値が100g/se
c・cm以上である部分架橋ポリアクリル酸 0.1〜
1.0重量% (b)  サルフェート基またはスルホネート基を有し
、かつオキシアルキル鎖を含有しない陰イオン性界面活
性剤の1種または2種以上 0.1〜5.0重量% fc)  炭素数10〜22の直鎖若しくは分岐鎖の飽
和若しくは不飽和脂肪酸またはそのアルカリ金属塩、ア
ルカリ土類金属塩もしくはアルカノールアミン塩 0.
05〜2.0重量%([+1  炭素数10〜22の直
鎖若しくは分岐鎖の飽和若しくは不飽和脂肪酸アルカノ
ールアミド0.1〜5.0重量% を必須成分として含有し、更に残部が1種以上の水不溶
性研磨剤と水であり、組成物のp++が6.0〜8.0
に調製された液体クレンザ−組成物を提供するものであ
る。
That is, the present invention has an average degree of polymerization of (al) of 103 to 103, and a Brookfield yield value of 0.3% by weight aqueous solution of 100 g/sec.
Partially crosslinked polyacrylic acid with ccm or more 0.1~
1.0% by weight (b) One or more anionic surfactants having a sulfate group or a sulfonate group and not containing an oxyalkyl chain 0.1 to 5.0% by weight fc) Number of carbon atoms 10-22 linear or branched saturated or unsaturated fatty acids or their alkali metal salts, alkaline earth metal salts or alkanolamine salts 0.
05 to 2.0% by weight ([+1 Contains 0.1 to 5.0% by weight of linear or branched saturated or unsaturated fatty acid alkanolamide having 10 to 22 carbon atoms as an essential component, and the remainder is 1 type. The above water-insoluble abrasive and water, and the p++ of the composition is 6.0 to 8.0.
The present invention provides a liquid cleanser composition prepared in accordance with the present invention.

(al成分の部分架橋ポリアクリル酸は平均重合度が1
03〜105.0.3重量%水溶液のプル・/クツイー
ルド降伏値が100g/sec−cm以上のものであり
、好ましくは100〜1000g/sec・cmのもの
である。ここでいうブルックフィールド降伏値とはポリ
アクリル酸の0.3重量%、pH6,0〜8.0(トリ
エタノールアミンで調整)水溶液の20℃の粘度を測定
し、次式より求めたものである。
(The partially crosslinked polyacrylic acid of the al component has an average degree of polymerization of 1
The pull/cut yield value of a 0.3% by weight aqueous solution is 100 g/sec-cm or more, preferably 100-1000 g/sec-cm. The Brookfield yield value referred to here is determined by measuring the viscosity at 20°C of an aqueous solution of 0.3% by weight of polyacrylic acid, pH 6.0 to 8.0 (adjusted with triethanolamine), and using the following formula. be.

ブルックフィールド降伏値は分子の架橋状況に関連した
数値で分子量が同じ場合この値が大きい程架橋されてい
ることを示す。
The Brookfield yield value is a numerical value related to the crosslinking state of molecules, and when the molecular weights are the same, the larger this value is, the more crosslinked the molecules are.

部分架橋ポリアクリル酸の配合量は0.1〜1.0重量
%好ましくは0.2〜0.5重量%組成物中に配合され
ることを要する。0.1重量%未満では粘度500cp
s以下となり、水不溶性研磨剤の長jtJ]保存安定性
が悪くなり、また1重量%を越えると粘度が5000c
ps以上と枯調となり使用上問題がある。
The amount of partially crosslinked polyacrylic acid to be blended in the composition is 0.1 to 1.0% by weight, preferably 0.2 to 0.5% by weight. Viscosity of less than 0.1% by weight is 500cp
s or less, the storage stability of the water-insoluble abrasive becomes poor, and if it exceeds 1% by weight, the viscosity decreases to 5000c.
If it exceeds ps, it becomes dry and there is a problem in use.

(b)成分のサルフェート基またはスルホネート基を有
し、かつオキシアルキル鎖を含有しない陰イオン性界面
活性剤を例示すれば、C8〜C24のアルキル基を有す
るアルキルベンゼンスルホネート、C8〜CI8のアル
キルサルフェート、C8〜Cl1lのアルケニルサルフ
ェート、cll””cz。のオレフィンスルホネート、
C6〜C1l+のアルカンスルホネート、C6〜C2□
のα−スルホ脂肪酸、C6〜C2□のα−スルホ脂肪酸
エステルおよび04〜C1゜のスルホコハク酸ジアルキ
ルエステル等のアルカリ金属塩、アルカリ土類金属塩、
アルカノールアミン塩等が挙げられ、これらは単独で用
いても良いし、2種以上混合しても良い。
Examples of the anionic surfactant having a sulfate group or a sulfonate group and not containing an oxyalkyl chain as the component (b) include alkylbenzene sulfonates having a C8 to C24 alkyl group, alkyl sulfates having a C8 to CI8; C8-Cl1l alkenyl sulfate, cll""cz. olefin sulfonate,
C6-C1l+ alkanesulfonate, C6-C2□
Alkali metal salts, alkaline earth metal salts such as α-sulfo fatty acids, C6 to C2□ α-sulfo fatty acid esters, and 04 to C1° sulfosuccinic acid dialkyl esters,
Examples include alkanolamine salts, and these may be used alone or in combination of two or more.

本発明において特に好ましいのはアルキルベンゼンスル
ホネート、オレフィンスルホネートのアルカリ金属塩、
またはアルカノールアミン塩である。
Particularly preferred in the present invention are alkylbenzene sulfonates, alkali metal salts of olefin sulfonates,
or an alkanolamine salt.

陰イオン性界面活性剤の配合量としては0.1〜5.0
重量%が好ましく、更に好ましくは0.3〜2.0重世
%である。0.1重量%未満では十分な汚垢分散力が得
られず、5重量%より多くなると泡切れ性が劣化するの
で好ましくない。
The blending amount of anionic surfactant is 0.1 to 5.0
It is preferably 0.3 to 2.0 weight %, more preferably 0.3 to 2.0 weight %. If it is less than 0.1% by weight, sufficient dirt dispersion power cannot be obtained, and if it is more than 5% by weight, the foam breaking property deteriorates, which is not preferable.

(c1成分の飽和若しくは不飽和脂肪酸又はそのアルカ
リ金属塩、アルカリ土類金属塩若しくはアルカノールア
ミン塩は天然のやし油、パーム油、牛脂などから誘導す
ることができ、また石油の酸化からも得られる。アルキ
ル鎖長はC6〜C2tが好ましい。配合量は0.05〜
2.0重量%、更に好ましくは0.1−0.5重量%の
範囲である。
(The c1 component, saturated or unsaturated fatty acid or its alkali metal salt, alkaline earth metal salt, or alkanolamine salt, can be derived from natural coconut oil, palm oil, beef tallow, etc., and can also be obtained from the oxidation of petroleum. The alkyl chain length is preferably C6 to C2t.The blending amount is 0.05 to
2.0% by weight, more preferably in the range of 0.1-0.5% by weight.

(d)成分の脂肪酸アルカノールアミドを例示すれば、
CI””CI8のアルキル基を有する脂肪酸モノエタノ
ールアミド、脂肪酸ジェタノールアミドが挙げられ、特
に好ましいのはC6〜C2tのアルキル鎖を有する脂肪
酸ジェタノールアミドである。またこのアシル残基は天
然産のグリセリド類、例えばやし油、パーム油、大豆油
、牛脂などから誘導することができる。また、例えば石
油の酸化またはフィッシャー・トロプシュ法による一酸
化炭素の水素添加によっても得られる。
Examples of the fatty acid alkanolamide of component (d) are:
Examples include fatty acid monoethanolamide and fatty acid jetanolamide having an alkyl group of CI""CI8, and particularly preferred is fatty acid jetanolamide having an alkyl chain of C6 to C2t. This acyl residue can also be derived from naturally occurring glycerides, such as coconut oil, palm oil, soybean oil, beef tallow, and the like. It can also be obtained, for example, by oxidation of petroleum or hydrogenation of carbon monoxide by the Fischer-Tropsch process.

配合量は0.1〜5:0重量%の範囲が好ましく、更に
好ましくは0.2〜1.5の範囲である。0.1重量%
未満では十分な汚垢分散力が得られず、5.0重量%を
越えると浄化槽の内部で発泡を生じるために好ましくな
い。
The blending amount is preferably in the range of 0.1 to 5:0% by weight, more preferably in the range of 0.2 to 1.5%. 0.1% by weight
If it is less than 5.0% by weight, sufficient dirt dispersion power will not be obtained, and if it exceeds 5.0% by weight, foaming will occur inside the septic tank, which is not preferable.

組成物のpHは浄化槽内の微生物への影響と肌への刺激
性の点から6.0〜8.0に調製されることが必要であ
る。
The pH of the composition needs to be adjusted to 6.0 to 8.0 from the viewpoint of influence on microorganisms in the septic tank and irritation to the skin.

水不溶性研磨剤を例示するならば、二酸化珪素、酸化ア
ルミニウム、酸化マグネシウム、酸化チタン、アルミノ
シリケート、炭化珪素、酸化鉄、珪石粉砕物、砂粉砕物
が挙げられる。これらは単独で用いても良いし、2種以
上混合しても良い。普通、研磨剤は組成物中に5〜55
重量%配合される。
Examples of water-insoluble abrasives include silicon dioxide, aluminum oxide, magnesium oxide, titanium oxide, aluminosilicate, silicon carbide, iron oxide, crushed silica, and crushed sand. These may be used alone or in combination of two or more. Typically, the abrasive is present in the composition in an amount of 5 to 55%.
% by weight is added.

また、本発明の実施に当たって、必要に応じて少量の香
料、顔料、染料、殺菌剤、可溶化剤を添加できる。
Further, in carrying out the present invention, small amounts of fragrances, pigments, dyes, bactericides, and solubilizers can be added as necessary.

〔実施例〕〔Example〕

以下に実施例により本発明を具体的に説明するが、本発
明はこれら実施例に限定されるものではない。
EXAMPLES The present invention will be specifically explained below with reference to Examples, but the present invention is not limited to these Examples.

表1に示す組成物を調製し、各組成物の、ABS樹脂へ
の悪影響を調べるための応力破壊試験、組成物の長期保
存安定性について以下の様に評価を行った。尚、表中の
組成は重量%で表した。
The compositions shown in Table 1 were prepared, and stress fracture tests were conducted to investigate the adverse effects of each composition on ABS resin, and the long-term storage stability of the compositions was evaluated as follows. In addition, the composition in the table is expressed in weight%.

〈試験法〉 ABS   ヒの心  U 下記条件で各組成物を試験し、終了後肉眼判定する。<Test method> ABS Hi no Kokoro U Each composition is tested under the following conditions, and visually judged after completion.

fil  テストピース ABS樹脂230mm X 35mm X 2 mm(
2)  条件 り 温  度−20℃ R1165% 接触時間=20Hr 潜在塗布ff1=1.3g/100mmx35nv+ 
(塗布面はガーゼでカバー) (3)  セソティッグ 第2図に示す様に塩ビパイプにテスト ピースを固定した。
fil Test piece ABS resin 230mm x 35mm x 2mm (
2) Conditioning temperature -20℃ R1165% Contact time = 20Hr Latent application ff1 = 1.3g/100mm x 35nv+
(Cover the coated surface with gauze) (3) Sesotig The test piece was fixed to a PVC pipe as shown in Figure 2.

(4)判定基準 ○ ひび・割れが認められない。(4) Judgment criteria ○ No cracks or cracks are observed.

× ひび・割れが認められる。× Cracks and cracks are observed.

五皿尿髪玄定株 下記条件で各組成物をガラス瓶で保存し、終了後に肉眼
判定した。
Each composition was stored in a glass bottle under the following conditions, and visually evaluated after storage.

(1)保存条件 温度=50.20、−5℃ 時間=20日間 (2)判定基準 ○ 分離していない。(1) Storage conditions Temperature = 50.20, -5℃ Time = 20 days (2) Judgment criteria ○ Not separated.

Δ 液の上面ににじみがある。Δ There is bleeding on the top of the liquid.

× 分離している。× Separated.

ン 2    (・       ) (11モデル汚れ作製 3cI11×8CII+の鉄テストピースに、ナタネ油
/カーボンブラック(重量比: 5/1)を1.0g塗
布した物を150℃で130分変性させたちの(鉛筆硬
度5B)を使用した。
(・) (Preparation of 11 model stains A 3cI11×8CII+ iron test piece was coated with 1.0g of rapeseed oil/carbon black (weight ratio: 5/1) and denatured at 150°C for 130 minutes. Pencil hardness 5B) was used.

(2)試験方法 モデル汚れの重量を秤量後、洗浄試験機に固定し、トイ
レクリナ−1gを用いてスポンジタワシで荷重1kgの
条件で100回往復洗浄を実施する。次に、このモデル
汚れを水洗し、乾燥後重量を秤量する。洗浄力は下記の
式から計算する。
(2) Test method After weighing the model soil, it was fixed in a cleaning tester and washed 100 times with a sponge scrubber using 1 g of toilet cleaner under a load of 1 kg. Next, this model stain is washed with water, dried, and weighed. The cleaning power is calculated using the formula below.

(3)標準洗剤組成 シリカ              1O00水   
             バランス
(3) Standard detergent composition Silica 1000 water
balance

【図面の簡単な説明】[Brief explanation of the drawing]

第1図は応力破壊試験における歪を示す図、第2図はテ
ストピースのセツティングを示す図である。 出願人代理人  古 谷   馨 第1図 −L 本歪  ε;□ し 第2図 テストピース /\
FIG. 1 is a diagram showing the strain in the stress fracture test, and FIG. 2 is a diagram showing the setting of the test piece. Applicant's agent Kaoru Furuya Figure 1-L Main strain ε;□ Figure 2 Test piece/\

Claims (1)

【特許請求の範囲】 1 液体クレンザーにおいて、 (a)平均重合度が10^3〜10^5で、0.3重量
%水溶液のブルックフィールド降伏値が100g/se
c・cm以上である部分架橋ポリアクリル酸0.1〜1
.0重量%(b)サルフェート基またはスルホネート基
を有し、かつオキシアルキル鎖を含有しない陰イオン性
界面活性剤の1種または2種以上0.1〜5.0重量% (c)炭素数10〜22の直鎖若しくは分岐鎖の飽和若
しくは不飽和脂肪酸またはそのアルカリ金属塩、アルカ
リ土類金属塩もしくはアルカノールアミン塩0.05〜
2.0重量% (d)炭素数10〜22の直鎖若しくは分岐鎖の飽和若
しくは不飽和脂肪酸アルカノールアミド0.1〜5.0
重量% を必須成分として含有し、更に残部が1種以上の水不溶
性研磨剤と水であり、組成物のpHが6.0〜8.0に
調製された液体クレンザー組成物。
[Scope of Claims] 1. A liquid cleanser, (a) having an average degree of polymerization of 10^3 to 10^5 and a Brookfield yield value of 0.3% by weight aqueous solution of 100 g/se;
Partially crosslinked polyacrylic acid having a particle size of c/cm or more 0.1 to 1
.. 0% by weight (b) 0.1 to 5.0% by weight of one or more anionic surfactants having a sulfate group or a sulfonate group and not containing an oxyalkyl chain (c) 10 to 5.0% by weight ~22 linear or branched saturated or unsaturated fatty acids or their alkali metal salts, alkaline earth metal salts or alkanolamine salts 0.05~
2.0% by weight (d) Straight chain or branched chain saturated or unsaturated fatty acid alkanolamide having 10 to 22 carbon atoms 0.1 to 5.0
% by weight as essential components, the balance being one or more water-insoluble abrasives and water, and the pH of the composition is adjusted to 6.0 to 8.0.
JP6892388A 1988-03-23 1988-03-23 Liquid cleanser composition Granted JPH01242697A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP6892388A JPH01242697A (en) 1988-03-23 1988-03-23 Liquid cleanser composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP6892388A JPH01242697A (en) 1988-03-23 1988-03-23 Liquid cleanser composition

Publications (2)

Publication Number Publication Date
JPH01242697A true JPH01242697A (en) 1989-09-27
JPH0524197B2 JPH0524197B2 (en) 1993-04-07

Family

ID=13387657

Family Applications (1)

Application Number Title Priority Date Filing Date
JP6892388A Granted JPH01242697A (en) 1988-03-23 1988-03-23 Liquid cleanser composition

Country Status (1)

Country Link
JP (1) JPH01242697A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0496999A (en) * 1990-08-10 1992-03-30 Kao Corp Liquid cleanser composition for use in toilet
EP0570226A2 (en) * 1992-05-13 1993-11-18 The Robert Mcbride Group Limited Cleaning compositions
EP0720646A4 (en) * 1993-09-23 1998-12-16 Clorox Co Thickened aqueous abrasive cleanser with improved rinsability

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR101634442B1 (en) * 2014-08-29 2016-06-29 주식회사 임진에스티 Axial force sensing device and method of bolt nut

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5474810A (en) * 1977-11-28 1979-06-15 Kao Corp Liquid cleanser composition
JPS54117506A (en) * 1978-03-06 1979-09-12 Kao Corp Liquid shampoo composition
JPS5638397A (en) * 1979-06-29 1981-04-13 Procter & Gamble Polishing agent containing liquid detergent composition and nonnclogging container for dispensing small amount
JPS6157695A (en) * 1984-08-30 1986-03-24 ライオン株式会社 Liquid detergent composition

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5474810A (en) * 1977-11-28 1979-06-15 Kao Corp Liquid cleanser composition
JPS54117506A (en) * 1978-03-06 1979-09-12 Kao Corp Liquid shampoo composition
JPS5638397A (en) * 1979-06-29 1981-04-13 Procter & Gamble Polishing agent containing liquid detergent composition and nonnclogging container for dispensing small amount
JPS6157695A (en) * 1984-08-30 1986-03-24 ライオン株式会社 Liquid detergent composition

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0496999A (en) * 1990-08-10 1992-03-30 Kao Corp Liquid cleanser composition for use in toilet
EP0570226A2 (en) * 1992-05-13 1993-11-18 The Robert Mcbride Group Limited Cleaning compositions
EP0570226A3 (en) * 1992-05-13 1994-08-24 Mcbride Robert Group Ltd Cleaning compositions
EP0720646A4 (en) * 1993-09-23 1998-12-16 Clorox Co Thickened aqueous abrasive cleanser with improved rinsability

Also Published As

Publication number Publication date
JPH0524197B2 (en) 1993-04-07

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