JPS5940198B2 - Improved solid detergent - Google Patents
Improved solid detergentInfo
- Publication number
- JPS5940198B2 JPS5940198B2 JP4095477A JP4095477A JPS5940198B2 JP S5940198 B2 JPS5940198 B2 JP S5940198B2 JP 4095477 A JP4095477 A JP 4095477A JP 4095477 A JP4095477 A JP 4095477A JP S5940198 B2 JPS5940198 B2 JP S5940198B2
- Authority
- JP
- Japan
- Prior art keywords
- amino acid
- salts
- acidic amino
- solid detergent
- salt
- 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
Links
Description
【発明の詳細な説明】
本発明は改良された固形洗剤に関するものであり、さら
に詳しく述べるならばN−長鎖アシル酸性アミノ酸塩を
基剤とする耐溶崩性および非付着性の改良された固形洗
剤に関するものである。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to an improved solid detergent, and more particularly to an improved dissolution-resistant and non-stick solid detergent based on an N-long chain acyl acidic amino acid salt. It concerns detergents.
N−長鎖アシル酸性アミノ酸塩を基剤とする固形洗剤は
、最近広く用いられるようになつているが、その理由と
して次のようなことが考えられる。すなわちN−長鎖ア
シル酸性アミノ酸塩を基剤とする固形洗剤は、成型性に
すぐれ、軟水のみならず硬水中でも良好な洗浄力を有し
、使用時の水溶液が皮膚と同等の弱酸性を呈するため皮
膚に対する刺激性が少なく、しかも使用後に肌にしつと
りとした感触を与えるなど従来の固形洗剤にないすぐれ
た特徴を有していることによるものと思われる。とくに
、従来の合成洗剤固形物に対し、その過度な脱脂力によ
る肌荒れを緩和するために湿潤性付与成分として保湿剤
(たとえば2−ピロリドンー5−カルボン酸ならびにそ
の塩、加水分解蛋白質、N−アセチルグリシンの塩類、
特開昭48−84108号公報に開示されている乳酸塩
またはグルタミン酸塩等)を配合することが通例であが
、これにくらべて、N−長鎖アシル酸性アミノ酸塩を基
剤とする固形洗剤は、基剤自体が皮膚に対して温和で刺
激性が少なく、しかも、使用後しつとりとした感触を皮
膚に与えるため、上記のような保湿剤を配合する必要の
ないことが大きな特徴である。しかしながら、N一長鎖
アシル酸性アミノ酸塩を基剤とする固形洗剤は、水と接
触すると溶け崩れて固形洗剤の形状を損う性質(以下溶
崩性と呼ぶ)と使用後石けん箱中に放置すると石けん箱
に付着する傾向(以下付着性と呼ぶ)があり.再使用の
際にセツケン箱から取出し難くなるという欠点がある。
N一長鎖アシル酸性アミノ酸塩を基剤とする固形洗剤に
おいて、溶崩性および付着性が大きいという欠点は、使
用感を損ね、固形洗剤としての商品価値を著しく低下さ
せるものである。このため、耐溶崩性および非付着性の
改良が強く望まれていた。従来、N一長鎖アシル酸性ア
ミノ酸塩を基剤とする固形洗剤の耐溶崩性および非付着
性を改良する方法として、コロイド状マグネシウムアル
ミニウムシリケートを添加する方法(特開昭49540
4号公報参照)およびN一長鎖アシル酸性アミノ酸のア
ルカリ土類金属塩等を添加する方法(特開昭50−16
0304号公報参照)などが開示されているが、改良効
果が不充分で、満足できる固形洗剤は得られなかつた。Solid detergents based on N-long chain acyl acidic amino acid salts have recently become widely used, and the following may be the reason for this. In other words, solid detergents based on N-long chain acyl acidic amino acid salts have excellent moldability, have good cleaning power not only in soft water but also in hard water, and when used, the aqueous solution exhibits weak acidity equivalent to that of the skin. This is thought to be due to the fact that it has excellent features not found in conventional solid detergents, such as being less irritating to the skin and leaving the skin feeling moisturized after use. In particular, for conventional solid synthetic detergents, moisturizers (e.g., 2-pyrrolidone-5-carboxylic acid and its salts, hydrolyzed protein, N-acetyl glycine salts,
Although it is customary to incorporate N-long chain acyl acidic amino acid salts (such as lactate or glutamate) as disclosed in JP-A-48-84108, solid detergents based on N-long chain acyl acidic amino acid salts The major feature of this product is that the base itself is mild and non-irritating to the skin, and it also leaves the skin with a moist feel after use, so there is no need to add a moisturizer as mentioned above. be. However, solid detergents based on N long-chain acyl acidic amino acid salts have the property of dissolving when they come into contact with water and damaging the shape of the solid detergent (hereinafter referred to as disintegrability), and they cannot be left in a soap box after use. Then, there is a tendency to adhere to the soap box (hereinafter referred to as adhesion). It has the disadvantage that it is difficult to remove it from the box when reusing it.
In solid detergents based on N long-chain acyl acidic amino acid salts, the drawbacks of high dissolution and adhesion impair the feeling of use and significantly reduce the commercial value of solid detergents. For this reason, improvements in melting resistance and non-adhesion properties have been strongly desired. Conventionally, a method of adding colloidal magnesium aluminum silicate to improve the dissolution resistance and non-adhesion of solid detergents based on N long-chain acyl acidic amino acid salts has been proposed (Japanese Patent Application Laid-open No. 49540
4) and a method of adding alkaline earth metal salts of N long-chain acyl acidic amino acids (see Japanese Patent Application Laid-open No. 50-16
However, the improvement effect was insufficient and a satisfactory solid detergent could not be obtained.
本発明者らは、N一長鎖アシル酸性アミノ酸塩を基剤と
する固形洗剤の耐溶崩性および非付着性を改良するため
、鋭意研究したところ、ある種のアミノ酸とその塩の添
加が有効であることを見出し、本発明を完成するに至つ
た。The present inventors conducted extensive research to improve the dissolution resistance and non-stick properties of solid detergents based on N long-chain acyl acidic amino acid salts, and found that the addition of certain amino acids and their salts is effective. We have discovered that this is the case, and have completed the present invention.
すなわち本発明は40〜99重量%の少なくとも1種の
N−長鎖アシル酸性アミノ酸塩を基剤とし、1〜60重
量%の酸性アミノ酸、酸性アミノ酸塩、塩基性アミノ酸
、および塩基性アミノ酸塩の少なくとも1種を改質剤と
して含むことを特徴とする、耐溶崩性および非付着性の
改良された固形洗剤を提供するものである。That is, the present invention is based on 40 to 99% by weight of at least one N-long chain acyl acidic amino acid salt, and 1 to 60% by weight of acidic amino acids, acidic amino acid salts, basic amino acids, and basic amino acid salts. The present invention provides a solid detergent with improved dissolution resistance and non-adherence, which is characterized by containing at least one modifier as a modifier.
本発明の基剤として用いられるN一長鎖アシル酸性アミ
ノ酸塩のアシル基は炭素数8ないし22の飽和または不
飽和の脂肪酸残基であることが好ましく、酸性アミノ酸
およびその塩は、それぞれがアスパラギン酸、グルタミ
ン酸、およびシステイン酸、並びにこれらのアミノ酸の
ナトリウム、カリウムなどのアルカリ金属塩、アンモニ
ウム塩、水溶性アミン塩6およびリジン、アルギニンな
どの塩基性アミノ酸塩から選ばれてもよい。The acyl group of the N long-chain acyl acidic amino acid salt used as the base of the present invention is preferably a saturated or unsaturated fatty acid residue having 8 to 22 carbon atoms, and the acidic amino acid and its salt each have asparagine It may be selected from acid, glutamic acid, and cysteic acid, and alkali metal salts such as sodium and potassium salts of these amino acids, ammonium salts, water-soluble amine salts 6 and basic amino acid salts such as lysine and arginine.
基剤の原料となる各酸性アミノ酸は、光学活性体および
ラセミ体のいずれでもよい。本発明の改質剤として用い
られるものは,酸性アミノ酸、酸性アミノ酸塩、塩基性
アミノ酸、および塩基性アミノ酸塩から選ばれる。Each acidic amino acid serving as a raw material for the base may be either an optically active form or a racemic form. The modifier used in the present invention is selected from acidic amino acids, acidic amino acid salts, basic amino acids, and basic amino acid salts.
酸性アミノ酸としては、アスパラギン酸およびグルタミ
ン酸が用いられ、塩基性アミノ酸としてはリジン、オル
ニチン、およびアルギニンなどが用いられる。また酸性
アミノ酸塩は、前記酸性アミノ酸のアルカリ金属塩、ア
ンモニウム塩、水溶性アミン塩、リジン、オルニチン、
アルギニンなどのような塩基性アミノ酸塩から選ぶこと
ができる。塩基性アミノ酸塩としては、前記塩基性アミ
ノ酸のアスパラギン酸、グルタミン酸などのような酸性
アミノ酸の塩、無機酸塩、および有機酸塩をあげること
ができる。Aspartic acid and glutamic acid are used as acidic amino acids, and lysine, ornithine, arginine, etc. are used as basic amino acids. The acidic amino acid salts include alkali metal salts, ammonium salts, water-soluble amine salts, lysine, ornithine,
It can be selected from basic amino acid salts such as arginine. Examples of the basic amino acid salt include salts of acidic amino acids such as aspartic acid and glutamic acid, inorganic acid salts, and organic acid salts of the basic amino acids.
本発明の改質剤として用いられるアミノ酸は光学活性体
、ラセミ体のいずれでもよい。本発明の改質剤の添加量
は、固形洗剤あたりlないし60wt%である。The amino acid used as the modifier of the present invention may be either an optically active form or a racemic form. The amount of the modifier of the present invention added is 1 to 60 wt% per solid detergent.
改質剤の添加量が1wt%以下では耐溶崩性および非付
着性の改良効果が少なく、60wt%以上では泡立ち、
洗浄力が低下し満足のゆく固形洗剤は得られない。本発
明の固形洗剤には、その需要目的に応じ、起泡増進剤、
粘結剤、香料、顔料、染料、その他固形洗剤に慣用され
ている補助剤(特公昭3710167号公報参照)を適
宜添加することができる。本発明の固形洗剤を製造する
には、基剤、改質剤、および必要に応じて補助剤を配合
したものに適当量の水を加え、これをロールおよび/ま
たはペレタイザ一で練つて型打ちをする石けん製造にお
ける機械練り方式を採用すればよい。If the amount of the modifier added is less than 1 wt%, the effect of improving melting resistance and non-adhesion is small, and if it is more than 60 wt%, foaming,
The cleaning power decreases and a satisfactory solid detergent cannot be obtained. The solid detergent of the present invention may include a foaming enhancer,
Binder, fragrance, pigment, dye, and other auxiliary agents commonly used in solid detergents (see Japanese Patent Publication No. 3710167) may be added as appropriate. To produce the solid detergent of the present invention, an appropriate amount of water is added to a mixture of a base, a modifier, and auxiliary agents as necessary, and the mixture is kneaded with a roll and/or pelletizer and molded. It is sufficient to adopt the machine kneading method used in soap manufacturing.
このようにして製造された本発明の固形洗剤は次のよう
な優れた性能を有する。(1)使用後石けん箱中に放置
しても石けん箱へ付着することがない。The solid detergent of the present invention produced in this way has the following excellent performance. (1) Even if it is left in the soap box after use, it will not stick to the soap box.
(2)水分の多い場所に置いても溶け崩れがない。(2) It will not melt or crumble even if placed in a humid place.
(3)摩擦溶解度は化粧用脂肪酸石けんと同等であり、
JISK−3301に適合する値を持ち、適度に溶ける
。(4)化粧用脂肪酸石けんのようなソフトな感じを肌
に与える。(3) The frictional solubility is equivalent to that of cosmetic fatty acid soap,
It has a value that complies with JISK-3301 and is moderately soluble. (4) Gives the skin a soft feel similar to cosmetic fatty acid soap.
(5)硬水に対しても良好な起泡力および洗浄力を有す
る。(5) It has good foaming power and detergency even in hard water.
(6)無刺激性で皮膚を荒さず、使用後の皮膚にしつと
りとした感触を与える。(6) It is non-irritating, does not irritate the skin, and gives a moist feel to the skin after use.
(7) N一長鎖アシルアミノ酸およびその塩に殺菌力
があるので、洗浄と同時に消毒も行える。(7) Since N long-chain acylamino acids and their salts have sterilizing power, they can be disinfected at the same time as cleaning.
(8) N一長鎖アシルアミノ酸または、その塩単独の
場合に比べて、非常にきめ細かなクリーム状の好ましい
泡を与える。以下実施例によつて本発明をさらに詳細に
説明する。(8) Provides a very fine creamy and desirable foam compared to the case of N long-chain acylamino acid or its salt alone. The present invention will be explained in more detail below using Examples.
例中の“部゛はすべて重量部である。実施例 1上記配
合物を小型ロールで充分混練した後、口金を45℃に保
つた小型石けん押出機で押出して得た棒状洗剤を足踏式
型打ち機で成型した。All "parts" in the examples are parts by weight.Example 1 After thoroughly kneading the above formulation in a small roll, a bar-shaped detergent obtained by extruding it in a small soap extruder with a nozzle kept at 45°C It was molded using a molding machine.
以下の各実施例、比較例、参考例の配合物も、実施例1
と同様に成型した。実施例 2
上記のようにして調製した実施例1〜3、比較例1〜3
、および参考例1の各固形洗剤について付着強度試験、
溶崩度試験、摩擦溶解度試験を行つた。The formulations of the following Examples, Comparative Examples, and Reference Examples are also Example 1
It was molded in the same way. Example 2 Examples 1 to 3 and Comparative Examples 1 to 3 prepared as described above
, and adhesion strength test for each solid detergent of Reference Example 1,
A dissolution test and a friction solubility test were conducted.
その結果を第1表に示す。なお各試験方法は次のとおり
である。(1)付着強度試験
固形洗剤の表面を水でぬらし、その上に針金をつけた直
径2.5CTILのポリエチレン製付着端子をのせ、2
4時間放置する。The results are shown in Table 1. The test methods are as follows. (1) Adhesive strength test Wet the surface of the solid detergent with water, place a polyethylene adhesive terminal with a diameter of 2.5 CTIL on top of it, and
Leave it for 4 hours.
最大秤量4kgのバネばかりのフツクを付着端子の針金
にかけ、バネばかりを引き、付着端子が固形洗剤から離
れたときのバネばかりの目盛を読み、その数値を付着強
度とした。各試料について測定を5回くり返し、その平
均値を求めた。(2)溶崩度試験
縦621nmX横45m11X幅207nmのプラスチ
ツク製石けん箱中に水5m1を入れ、その中に50mm
×35X10mm、重量207に成形した固形洗剤を浸
し、24時間放置した後固形洗剤の崩れ方を観察した。A hook with a spring balance with a maximum weight of 4 kg was hung on the wire of the adhesive terminal, the spring balance was pulled, and the scale on the spring balance when the adhesive terminal was separated from the solid detergent was read, and the value was taken as the adhesive strength. The measurement was repeated five times for each sample, and the average value was determined. (2) Dissolution degree test Pour 5ml of water into a plastic soap box measuring 621nm long x 45m11 x width 207nm, and add 50mm water inside it.
A solid detergent molded to a size of 35 x 10 mm and a weight of 207 mm was immersed, and after being left for 24 hours, the way the solid detergent crumbled was observed.
評価方法は、ほぼ原形をとどめているものを0、少し崩
れているものを△、完全に崩れているものをXとした。The evaluation method was as follows: 0 if the shape remained almost the same, △ if the shape was slightly collapsed, and X if the shape was completely collapsed.
測定は各試料について3回づつ行い、その平均により評
価した。(3)摩擦溶解度試験
JISK−3304(1956)に準じて測定した。The measurement was performed three times for each sample, and the evaluation was based on the average. (3) Friction solubility test Measured according to JISK-3304 (1956).
結果を第1表に示す。実施例1〜3の固形洗剤は泡立ち
がよく、洗浄後の皮膚にしつとりとした感触を与え、刺
激が少なく、非付着性および耐溶崩性がすぐれ、摩擦溶
解度も良好であつた。The results are shown in Table 1. The solid detergents of Examples 1 to 3 foamed well, gave a moist feel to the skin after washing, were less irritating, had excellent non-stick properties and disintegration resistance, and had good friction solubility.
実施例 4
実施例4〜9の各固形洗剤の付着強度、溶崩度、摩擦溶
解度を測定した結果を第2表に示す。Example 4 Table 2 shows the results of measuring the adhesion strength, degree of dissolution, and frictional solubility of each of the solid detergents of Examples 4 to 9.
Claims (1)
ル酸性アミノ酸塩からなる基剤と、1〜60重量%の酸
性アミノ酸、酸性アミノ酸塩、塩基性アミノ酸、および
塩基性アミノ酸塩からなる群より選ばれた少なくとも1
種からなる改質剤とを含んでなることを特徴とする耐溶
崩性および非付着性の改良された固形洗剤。 2 前記N−長鎖アシル酸性アミノ酸塩のアシル基が炭
素数8ないし22の飽和または不飽和の脂肪酸残基であ
る特許請求の範囲第1項記載の固形洗剤。 3 前記N−長鎖アシル酸性アミノ酸塩がアスパラギン
酸塩、グルタミン酸塩、およびシステイン酸塩、から選
ばれる特許請求の範囲第1項記載の固形洗剤。 4 前記N−長鎖アシル酸性アミノ酸塩が、アルカリ金
属塩、アンモニウム塩、水溶性アミン塩、および塩基性
アミノ酸塩から選ばれる特許請求の範囲第1項記載の固
形洗剤。 5 前記酸性アミノ酸および酸性アミノ酸塩が、それぞ
れアスパラギン酸またはグルタミン酸および、アスパラ
ギン酸塩または、グルタミン酸塩である特許請求の範囲
第1項記載の固形洗剤。 6 前記塩基性アミノ酸および塩基性アミノ酸塩がそれ
ぞれリジン、オルニチン、またはアルギニン、および、
リジン塩、オルニチン塩、またはアルギニン塩である特
許請求の範囲第1項記載の固形洗剤。 7 前記酸性アミノ酸塩が、アルカリ金属塩、アンモニ
ウム塩、水溶性アミン塩、および塩基性アミノ酸塩から
なる群より選ばれる特許請求の範囲第1項記載の固形洗
剤。 8 前記塩基性アミノ酸塩が、酸性アミノ酸塩、無機酸
塩、および有機酸塩から選ばれる特許請求の範囲第1項
記載の固形洗剤。[Scope of Claims] 1. A base consisting of 40 to 99% by weight of at least one N-long chain acyl acidic amino acid salt, and 1 to 60% by weight of an acidic amino acid, an acidic amino acid salt, a basic amino acid, and a base. at least one selected from the group consisting of amino acid salts
1. A solid detergent having improved disintegration resistance and non-adherence, characterized by comprising a modifier consisting of seeds. 2. The solid detergent according to claim 1, wherein the acyl group of the N-long chain acyl acidic amino acid salt is a saturated or unsaturated fatty acid residue having 8 to 22 carbon atoms. 3. The solid detergent of claim 1, wherein the N-long chain acyl acidic amino acid salt is selected from aspartate, glutamate, and cysteate. 4. The solid detergent according to claim 1, wherein the N-long chain acyl acidic amino acid salt is selected from alkali metal salts, ammonium salts, water-soluble amine salts, and basic amino acid salts. 5. The solid detergent according to claim 1, wherein the acidic amino acid and acidic amino acid salt are aspartic acid or glutamic acid and aspartate or glutamate, respectively. 6 The basic amino acid and the basic amino acid salt are each lysine, ornithine, or arginine, and
The solid detergent according to claim 1, which is a lysine salt, an ornithine salt, or an arginine salt. 7. The solid detergent according to claim 1, wherein the acidic amino acid salt is selected from the group consisting of alkali metal salts, ammonium salts, water-soluble amine salts, and basic amino acid salts. 8. The solid detergent according to claim 1, wherein the basic amino acid salt is selected from acidic amino acid salts, inorganic acid salts, and organic acid salts.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP4095477A JPS5940198B2 (en) | 1977-04-12 | 1977-04-12 | Improved solid detergent |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP4095477A JPS5940198B2 (en) | 1977-04-12 | 1977-04-12 | Improved solid detergent |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS53126006A JPS53126006A (en) | 1978-11-02 |
JPS5940198B2 true JPS5940198B2 (en) | 1984-09-28 |
Family
ID=12594879
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP4095477A Expired JPS5940198B2 (en) | 1977-04-12 | 1977-04-12 | Improved solid detergent |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS5940198B2 (en) |
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DE112017006590T5 (en) | 2016-12-27 | 2019-09-05 | Yazaki Corporation | Crimp connection and method for making the crimp connection |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5628297A (en) * | 1979-08-14 | 1981-03-19 | Kawaken Fine Chemicals Co | Aqueous detergent composition |
JP4644493B2 (en) * | 2003-01-07 | 2011-03-02 | 株式会社ピーアンドピーエフ | Surfactant composition and detergent composition and emulsified composition using the same |
JP2005325243A (en) * | 2004-05-14 | 2005-11-24 | Asahi Kasei Chemicals Corp | Cleanser composition |
DE102006008757A1 (en) * | 2006-02-24 | 2007-08-30 | Daimlerchrysler Ag | Water pump, for a vehicle motor, is within the hollow zone of the function wheel journal coupled to a drive by a shaft through the journal wall |
ITVR20130202A1 (en) * | 2013-08-27 | 2015-02-28 | Euro Kemical S R L | N-ACYL SALT-BASED AMINO ACIDS WITH AMINO ACIDS OR AMINO BASILICLES |
-
1977
- 1977-04-12 JP JP4095477A patent/JPS5940198B2/en not_active Expired
Cited By (7)
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WO2018123101A1 (en) | 2016-12-27 | 2018-07-05 | 矢崎総業株式会社 | Crimp terminal |
WO2018123099A1 (en) | 2016-12-27 | 2018-07-05 | 矢崎総業株式会社 | Crimp terminal |
WO2018123097A1 (en) | 2016-12-27 | 2018-07-05 | 矢崎総業株式会社 | Terminal-equipped electric wire and terminal production method |
WO2018123102A1 (en) | 2016-12-27 | 2018-07-05 | 矢崎総業株式会社 | Crimp terminal |
WO2018123098A1 (en) | 2016-12-27 | 2018-07-05 | 矢崎総業株式会社 | Terminal connection method |
DE112017006590T5 (en) | 2016-12-27 | 2019-09-05 | Yazaki Corporation | Crimp connection and method for making the crimp connection |
US10978824B2 (en) | 2016-12-27 | 2021-04-13 | Yazaki Corporation | Crimp terminal with ridge portion and manufacturing method thereof |
Also Published As
Publication number | Publication date |
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JPS53126006A (en) | 1978-11-02 |
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