JP3523101B2 - Deodorant cleaning agent - Google Patents

Deodorant cleaning agent

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Publication number
JP3523101B2
JP3523101B2 JP01555199A JP1555199A JP3523101B2 JP 3523101 B2 JP3523101 B2 JP 3523101B2 JP 01555199 A JP01555199 A JP 01555199A JP 1555199 A JP1555199 A JP 1555199A JP 3523101 B2 JP3523101 B2 JP 3523101B2
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JP
Japan
Prior art keywords
acid
weight
carbon atoms
hlb
koh
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JP01555199A
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Japanese (ja)
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JP2000212594A (en
Inventor
勝幸 高野
一成 丸田
成 田村
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Kao Corp
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Kao Corp
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Description

【発明の詳細な説明】 【0001】 【発明の属する技術分野】本発明は、食器、まな板、包
丁、魚焼きグリル、スポンジ等の台所用品向けの消臭洗
浄剤に関する。 【0002】 【従来の技術及び発明が解決しようとする課題】食器、
まな板等の硬質表面には、生魚等の臭気が残りやすく、
洗浄により完全に除去することは難しい。生魚等の食品
由来の不快臭は、アンモニアに代表されるアミン系化合
物、酢酸、酪酸等の低級脂肪酸化合物、メルカプタンに
代表されるイオウ化合物が原因であり、特にアミン系化
合物は、1回の洗浄ではなかなか除去できない不快臭の
1つである。その理由は、臭気物質が油やワックス等の
油性物質に取り込まれた状態で硬質表面に付着している
ためと考えられる。 【0003】消臭性能を有する洗浄剤としては、特開平
9−137194号公報に植物性の消臭成分を配合した
ものや、特開平8−302393号公報に特定の界面活
性剤とキレート剤を配合したものが開示されているが、
これらの洗浄剤では、食品由来の臭気を十分に除去する
ことはできなかった。 【0004】本発明は、まな板や食器等の硬質表面に付
着した臭気の消臭方法を提供することを目的とする。 【0005】 【課題を解決するための手段】本発明は、下記(a)、
(b)、(c)成分及び水を含有し、(b)成分と
(c)成分の合計量が0.5〜20重量%で、かつ重量
比が(b)/(c)=10/90〜90/10である消
臭洗浄剤を提供する。 (a)アルキルグリコシド 0.1〜40重量% (b)ポリカルボン酸型界面活性剤 (c)1以上のカルボキシル基を有する炭素数が3〜7
の化合物 【0006】 【発明の実施の形態】本発明で用いる(a)成分のアル
キルグリコシドは、炭素数が8〜18のアルキル基又は
アルケニル基を1つ有し、糖の縮合度が1〜10のもの
が好ましく、具体的には特開平2−247299号公報
の3頁左下欄4行〜4頁右上欄6行に記載のものが挙げ
られ、下記一般式(I)で表されるものがより好まし
い。 【0007】R1(OR2xy (I) [式中、R1は炭素数8〜18の直鎖又は分岐鎖のアル
キル基又はアルケニル基を示し、R2は炭素数2〜4の
アルキレン基を示し、Gは炭素数5〜6の還元糖に由来
する残基を示し、xはその平均値が0〜5となる数を示
し、yはその平均値が1〜10となる数を示す。] 一般式(I)において、R1は溶解性、起泡性及び洗浄性
の点から、直鎖が好ましく、炭素数は10〜14が好ま
しい。R2は溶解性の点から、炭素数は2〜3が好まし
い。xは平均値で0〜2が好ましい。yは平均値で1〜
1.5が好ましい。yの値(糖縮合度)は、特開平8−
53696号公報の6頁10欄26行目〜7頁11欄1
5行目の記載に基づいてNMRにより測定できる。Gは
グルコース由来の残基が好ましい。(a)成分の含有量
は、0.1〜40重量%、好ましくは0.5〜30重量%
である。 【0008】本発明で用いる(b)成分のポリカルボン
酸型界面活性剤は、分子中に2以上、好ましくは2又は
3のカルボキシル基と、炭素数8〜20のアルキル基又
はアルケニル基を有し、かつデービス法(界面活性剤
物性・応用・化学生態学,北原文雄ら著,講談社サイエ
ンティフィック 第7刷発行,P24〜27に記載の方
法により測定)で求めたHLBが、カルボン酸の状態で
4〜15、好ましくは4〜10の性質を示すものが好ま
しい。(b)成分のポリカルボン酸型界面活性剤は、一
般式(II)で表される化合物がより好ましい。 【0009】 【化1】 【0010】[式中、R3はアミド基で分断されていても
よい炭素数10〜18のアルキル基又はアルケニル基で
あり、R4、R5、R6はそれぞれ独立に水素、メチル基
又はエチル基を示し;R7は水素、C24OH又はCO
OM(ここでMは水素、アルカリ金属又はアルカリ土類
金属を示す。)を示し;Xはメチレン基、アミノ基、エ
ーテル基を示し;l、m、nはそれぞれ独立に0又は1
を示し;p、q、rは0、1又は2で、p+q+r=3
となる数を示し(ただし、Xがメチレン基又はエーテル
基の場合は、p及びqは1又は2を示す。);R3
4、R5、R6、R7、X、l、m、n、p、q、rは上
記のデービス法で求めたHLBが4〜15になるように
選ばれるものである。ただし、HLBはMを水素として
求めるものとする]。 【0011】特に、このポリカルボン酸型界面活性剤
は、酸の状態として重量分当たりの酸価が、300〜6
00mgKOH/gのものが好ましく、特に300〜5
00mgKOH/gのものが好ましい。酸価の測定方法
は酸の状態で0.5gをトルエン/エタノール(容量比
50/50、フェノールフタレイン0.5重量%添加)
溶媒50mgに溶解させ、0.1NのKOHで滴定し、
フェノールフタレインが着色した時点を終点とし、要し
たKOHの量をmgで表した数値である。 【0012】ポリカルボン酸型界面活性剤の好ましい具
体例としては、下記式(1)〜(6)で表される化合物
の塩が挙げられ、その中でも特に(4)〜(6)のもの
が消臭性能の点で好ましい。なお、ポリカルボン酸型界
面活性剤は一部又は全部がアルカリ金属、アルカリ土類
金属、アルカノールアミンによる塩になっているもので
あり、pH条件により消臭洗浄剤中で一部酸の状態で存
在してもよい。 【0013】 【化2】 【0014】[式中、R8は炭素数8〜20のアルキル基
又はアルケニル基で、上記HLB及び酸価を満足するよ
うに選ばれる]。 【0015】本発明で用いる(c)成分の1以上のカル
ボキシル基を有する炭素数が3〜7の化合物は、乳酸、
グルコン酸、コハク酸、グルタル酸、アジピン酸、リン
ゴ酸、酒石酸、マレイン酸、フマル酸、イタコン酸、ク
エン酸、安息香酸、サリチル酸及びそれらの塩、グリシ
ン、アラニン、バリン、ロイシン、セリン、グルタミン
酸、アスパラギン酸等のアミノ酸及びそれらの塩が好ま
しい。これらのうち、乳酸、コハク酸、リンゴ酸、酒石
酸、クエン酸、安息香酸、グリシン、アラニン、バリ
ン、ロイシン、セリン、グルタミン酸、アスパラギン酸
及びこれらの塩がより好ましい。 【0016】(b)成分と(c)成分の含有量は、合計
で0.5〜20重量%、好ましくは3〜15重量%、よ
り好ましくは5〜15重量%で、重量比が(b)/
(c)=10/90〜90/10、好ましくは20/8
0〜80/20、より好ましくは50/50〜80/2
0である。 【0017】本発明ではさらに他の界面活性剤として、
アルキル硫酸エステル塩、直鎖アルキルベンゼンスルホ
ン酸塩、α−スルホ脂肪酸メチルエステル塩、α−オレ
フィンスルホン酸塩、アルカンスルホン酸塩、脂肪酸塩
等の陰イオン界面活性剤、ポリオキシアルキレンアルキ
ルエーテル、脂肪族アルカノールアミド等の非イオン界
面活性剤、アルキルヒドロキシスルホベタイン等の両性
界面活性剤を配合することができる。 【0018】また、可溶化剤としてエタノール、イソプ
ロパノール等の低級アルコール類、エチレングリコー
ル、プロピレングリコール、グリセリン、ソルビトール
等の多価アルコール類、p−トルエンスルホン酸塩、m
−キシレンスルホン酸塩等の芳香族スルホン酸塩等を配
合することができ、さらに香料、防腐・防黴剤を配合す
ることが好ましい。 【0019】本発明の消臭洗浄剤は、残部は水であり、
液状が好ましいが、均一な溶液以外にエマルション型や
液晶小滴又は固体を分散させたようなものでもよく、そ
の他の形態のものであっても使用上不都合のない流動性
のあるものであればよい。粘度は用途に応じた状態に適
宜調整される。 【0020】本発明の消臭洗浄剤のpHは、食材臭に効
果的な消臭性能を得るために、25℃における原液のp
Hが、好ましくは5.0〜9.0、より好ましくは6.
0〜8.0である。pHの調整には、酸剤として硫酸、
塩酸及びカルボン酸基を有する有機酸から選ばれる1種
以上を用いることが好ましく、アルカリ剤としてアルカ
リ金属の水酸化物、アルカノールアミンから選ばれる1
種以上を用いることが好ましい。 【0021】本発明の消臭洗浄剤は、原液をそのままス
ポンジやタオル等にとって洗浄する方法、汚れに直接吹
き付けることによって洗浄する方法が効果的であり、水
等で100倍まで希釈しても十分な洗浄及び消臭性能を
発揮できる。 【0022】 【実施例】実施例1〜4、比較例1〜2 表1に示す各成分を用い、消臭洗浄剤を得た。原液のp
Hは塩酸水溶液と水酸化ナトリウム水溶液で調整した。
(a−1)、(a−2)、(b−1)〜(b−3)成分
及び各評価方法の詳細は下記のとおりである。結果を表
1に示す。 (a−1)一般式(I)においてR1=カプリル基、x=
0、G=グルコース残基、y=1.3 (a−2)一般式(I)においてR1=ドデシル基、x=
0、G=グルコース残基、y=1.3 (b−1) 【0023】 【化3】 【0024】(HLB=12.1,酸価=314)イミ
ノジ酢酸ナトリウム177.1g、エタノール100
g、イオン交換水100g、1―クロロヘキサデカン2
60.9gを3つ口フラスコに入れ、90℃で5時間反
応させた。反応終了後エタノール及び水を留去し、得ら
れた固形物をヘキサンで洗浄し、乾燥させて、(b−
1)成分70重量%を含有する混合物を得た。 (b−2) 【0025】 【化4】 【0026】(HLB=6.2,酸価=367)クエン
酸96.1g(105℃、26.7kPaで5時間乾燥
させたもの)、アクリロニトリル200gを4つ口フラ
スコに入れ、80℃まで昇温した。ステアリン酸クロリ
ド151.5gを3時間かけて滴下し、この時発生する
塩酸を窒素ガスを流しながら留去した。さらに3時間窒
素ガスを流した後、アセトニトリルを減圧留去し、得ら
れた固形分をエタノールで再結晶して、(b−2)成分
60重量%を含有する混合物を得た。 (b−3) 【0027】 【化5】 【0028】(HLB=5.9,酸価=371)ドデシ
ルアルコール372.6g、NaOH2gを4つ口フラ
スコに入れ、120℃まで昇温した後、26.7kPa
の減圧下、生成する水を除去しながら3時間反応させ
た。窒素ガスを流入しながら常圧にもどした後、コハク
酸ジエチル87.1gを1時間かけて滴下した。熟成3
時間後、20℃まで冷却し、反応混合物にエタノール3
00g、イオン交換水200g、水酸化ナトリウム90
gを添加し、90℃で2時間反応させた。20℃まで冷
却後、イオン交換水2000ml、ヘキサン1500m
l、20%硫酸水溶液563.5gを添加し、攪拌中和
した。ヘキサン層をイオン交換水で洗浄後、蒸留を行
い、(b−3)成分60重量%を含有する混合物を得
た。 【0029】<消臭性能評価>まな板(23.0×41.
0×1.5cm、材質:ポリエチレン)上でイワシの切
り身10gを細かく切り刻んだ後、固形分を取り除き、
水でまな板表面を軽くすすいだ。表1の洗浄剤3g及び
水(硬度3.5DH、Mgイオン/Caイオン=1/3
の調整水を使用)27gを染み込ませたスポンジ(1
0.5×7.5×4.0cm、材質:ポリウレタンフォー
ム)を用いて、まな板表面を均等に3分間手洗い洗浄し
た。30歳代の男性及び女性10人(各5人ずつ)のパ
ネルに洗浄後のまな板の臭いを嗅いでもらい、臭いが感
知されない場合を2点、臭いが感知された場合を1点と
し、パネル10人の平均点が1.75点以上を○、1.5
点以上1.75点未満を△、1.5点未満を×として消臭
性能を評価した。 【0030】 【表1】【0031】 【発明の効果】本発明の消臭洗浄剤は、食器、まな板、
包丁、魚焼きグリル、スポンジ等の洗浄対象物に付着し
た食材臭に対する洗浄力及び消臭性能が優れる。
Description: BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a deodorant detergent for kitchenware such as tableware, cutting boards, kitchen knives, grilled fish, sponges and the like. [0002] Tableware,
On the hard surface of cutting boards etc., the odor of raw fish etc. tends to remain,
It is difficult to completely remove by washing. Unpleasant odors derived from foods such as raw fish are caused by amine compounds represented by ammonia, lower fatty acid compounds such as acetic acid and butyric acid, and sulfur compounds represented by mercaptan. Particularly, amine compounds are washed once. This is one of the unpleasant odors that cannot be easily removed. It is considered that the reason is that the odorous substance is attached to the hard surface in a state of being taken in an oily substance such as oil or wax. [0003] Detergents having a deodorizing performance include those in which a plant deodorant component is blended in JP-A-9-137194, and specific surfactants and chelating agents disclosed in JP-A-8-302393. Although the blended one is disclosed,
With these cleaning agents, the odor derived from food could not be sufficiently removed. An object of the present invention is to provide a method for deodorizing odors attached to hard surfaces such as cutting boards and tableware. The present invention provides the following (a):
It contains components (b) and (c) and water, the total amount of components (b) and (c) is 0.5 to 20% by weight, and the weight ratio is (b) / (c) = 10 / The present invention provides a deodorant detergent having a 90 to 90/10 ratio. (A) alkyl glycoside 0.1 to 40% by weight (b) polycarboxylic acid surfactant (c) 3 to 7 carbon atoms having one or more carboxyl groups
DETAILED DESCRIPTION OF THE INVENTION The alkyl glycoside of the component (a) used in the present invention has one alkyl or alkenyl group having 8 to 18 carbon atoms, and has a degree of condensation of sugar of 1 to 1. 10 are preferable, and specific examples include those described in JP-A-2-247299, page 3, lower left column, line 4 to page 4, upper right column, line 6, and represented by the following general formula (I). Is more preferred. R 1 (OR 2 ) x G y (I) wherein R 1 represents a linear or branched alkyl or alkenyl group having 8 to 18 carbon atoms, and R 2 represents 2 to 4 carbon atoms. G represents a residue derived from a reducing sugar having 5 to 6 carbon atoms, x represents a number having an average value of 0 to 5, and y represents an average value of 1 to 10. Indicates a number. In the general formula (I), R 1 is preferably a straight chain, and preferably has 10 to 14 carbon atoms from the viewpoint of solubility, foaming properties, and detergency. R 2 preferably has 2 to 3 carbon atoms from the viewpoint of solubility. x is preferably 0 to 2 on average. y is an average value of 1 to
1.5 is preferred. The value of y (the degree of sugar condensation) is described in
No. 53696, page 6, column 10, line 26 to page 7, column 11, column 1
It can be measured by NMR based on the description in the fifth line. G is preferably a residue derived from glucose. The content of the component (a) is 0.1 to 40% by weight, preferably 0.5 to 30% by weight.
It is. The polycarboxylic acid type surfactant (b) used in the present invention has at least two, preferably two or three, carboxyl groups and an alkyl or alkenyl group having 8 to 20 carbon atoms in the molecule. And Davis method (surfactant
HLB determined by the method described in “Physical Properties / Application / Chemical Ecology”, written by Fumio Kitahara et al., Published by Kodansha Scientific, 7th printing, pages 24 to 27) is 4 to 15, preferably 4 in the carboxylic acid state. Those exhibiting properties of from 10 to 10 are preferred. As the polycarboxylic acid surfactant of the component (b), a compound represented by the general formula (II) is more preferable. [0009] Wherein R 3 is an alkyl or alkenyl group having 10 to 18 carbon atoms which may be interrupted by an amide group, and R 4 , R 5 and R 6 are each independently hydrogen, methyl or Represents an ethyl group; R 7 is hydrogen, C 2 H 4 OH or CO
OM (where M represents hydrogen, an alkali metal or an alkaline earth metal); X represents a methylene group, an amino group or an ether group; l, m and n each independently represent 0 or 1
Where p, q, and r are 0, 1 or 2, and p + q + r = 3
(However, when X is a methylene group or an ether group, p and q represent 1 or 2); R 3 ,
R 4 , R 5 , R 6 , R 7 , X, l, m, n, p, q, and r are selected so that the HLB determined by the above Davis method is 4 to 15. However, it is assumed that HLB determines M as hydrogen.] Particularly, the polycarboxylic acid type surfactant has an acid value of 300 to 6 as an acid state per weight.
00 mgKOH / g is preferable, and especially 300 to 5
Those having a concentration of 00 mg KOH / g are preferred. The acid value is measured by adding 0.5 g of the acid in toluene / ethanol (volume ratio 50/50, phenolphthalein 0.5% by weight).
Dissolve in 50 mg of solvent, titrate with 0.1 N KOH,
The end point is the time when phenolphthalein is colored, and the required amount of KOH is a numerical value expressed in mg. Preferable specific examples of the polycarboxylic acid type surfactant include salts of compounds represented by the following formulas (1) to (6), and among them, those of (4) to (6) are particularly preferable. It is preferable in terms of deodorizing performance. Incidentally, the polycarboxylic acid type surfactant is partly or wholly in the form of a salt with an alkali metal, an alkaline earth metal, or an alkanolamine. May be present. [0013] [Wherein, R 8 is an alkyl or alkenyl group having 8 to 20 carbon atoms and is selected so as to satisfy the above HLB and acid value]. The compound (c) having at least one carboxyl group and having 3 to 7 carbon atoms, which is used in the present invention, is lactic acid,
Gluconic acid, succinic acid, glutaric acid, adipic acid, malic acid, tartaric acid, maleic acid, fumaric acid, itaconic acid, citric acid, benzoic acid, salicylic acid and salts thereof, glycine, alanine, valine, leucine, serine, glutamic acid, Amino acids such as aspartic acid and salts thereof are preferred. Of these, lactic acid, succinic acid, malic acid, tartaric acid, citric acid, benzoic acid, glycine, alanine, valine, leucine, serine, glutamic acid, aspartic acid and salts thereof are more preferred. The total content of the components (b) and (c) is 0.5 to 20% by weight, preferably 3 to 15% by weight, more preferably 5 to 15% by weight, and the weight ratio is (b). ) /
(C) = 10/90 to 90/10, preferably 20/8
0-80 / 20, more preferably 50 / 50-80 / 2
0. In the present invention, as another surfactant,
Anionic surfactants such as alkyl sulfate esters, linear alkyl benzene sulfonates, α-sulfofatty acid methyl ester salts, α-olefin sulfonates, alkane sulfonates, and fatty acid salts, polyoxyalkylene alkyl ethers, and aliphatics A nonionic surfactant such as alkanolamide and an amphoteric surfactant such as alkylhydroxysulfobetaine can be blended. As a solubilizer, lower alcohols such as ethanol and isopropanol, polyhydric alcohols such as ethylene glycol, propylene glycol, glycerin and sorbitol, p-toluenesulfonic acid salt,
-An aromatic sulfonate such as xylene sulfonate can be blended, and it is preferable to further blend a fragrance and an antiseptic / antifungal agent. The deodorant detergent of the present invention has water as the balance,
A liquid is preferable, but an emulsion-type liquid crystal droplet or a solid other than a uniform solution may be dispersed, or any other form may be used as long as there is no inconvenience in use. Good. The viscosity is appropriately adjusted according to the application. The pH of the deodorant detergent of the present invention is determined by adjusting the pH of the stock solution at 25 ° C. in order to obtain an effective deodorant effect on food odor.
H is preferably 5.0 to 9.0, more preferably 6.
0 to 8.0. To adjust the pH, sulfuric acid as an acid agent,
It is preferable to use at least one selected from hydrochloric acid and an organic acid having a carboxylic acid group, and one selected from alkali metal hydroxides and alkanolamines as alkali agents.
It is preferred to use more than one species. The deodorant cleaning agent of the present invention is effective in a method of washing the undiluted solution as it is with a sponge or a towel, and a method of washing by directly spraying it on dirt. Demonstrates excellent cleaning and deodorizing performance. Examples 1 to 4 and Comparative Examples 1 to 2 Deodorizing detergents were obtained using the components shown in Table 1. Stock solution p
H was adjusted with a hydrochloric acid aqueous solution and a sodium hydroxide aqueous solution.
Details of the components (a-1), (a-2), (b-1) to (b-3) and the respective evaluation methods are as follows. Table 1 shows the results. (A-1) In the general formula (I), R 1 = capryl group, x =
0, G = glucose residue, y = 1.3 (a-2) In the general formula (I), R 1 = dodecyl group, x =
0, G = glucose residue, y = 1.3 (b-1) (HLB = 12.1, acid value = 314) 177.1 g of sodium iminodiacetate, 100 parts of ethanol
g, 100 g of ion-exchanged water, 1-chlorohexadecane 2
60.9 g was placed in a three-necked flask and reacted at 90 ° C. for 5 hours. After completion of the reaction, ethanol and water were distilled off, and the obtained solid substance was washed with hexane, dried, and treated with (b-
1) A mixture containing 70% by weight of the components was obtained. (B-2) (HLB = 6.2, acid value = 367) 96.1 g of citric acid (dried at 105 ° C., 26.7 kPa for 5 hours) and 200 g of acrylonitrile are placed in a four-necked flask and heated to 80 ° C. Warmed up. 151.5 g of stearic acid chloride was added dropwise over 3 hours, and hydrochloric acid generated at this time was distilled off while flowing nitrogen gas. After further flowing nitrogen gas for 3 hours, acetonitrile was distilled off under reduced pressure, and the obtained solid was recrystallized with ethanol to obtain a mixture containing the component (b-2) at 60% by weight. (B-3) (HLB = 5.9, acid value = 371) Dodecyl alcohol (372.6 g) and NaOH (2 g) were placed in a four-necked flask, heated to 120 ° C., and then heated to 26.7 kPa.
The reaction was carried out for 3 hours while removing generated water under reduced pressure. After returning to normal pressure while flowing nitrogen gas, 87.1 g of diethyl succinate was added dropwise over 1 hour. Aging 3
After an hour, cool to 20 ° C. and add ethanol 3 to the reaction mixture.
00g, ion exchange water 200g, sodium hydroxide 90
g was added and reacted at 90 ° C. for 2 hours. After cooling to 20 ° C, ion exchange water 2000ml, hexane 1500m
1 and 563.5 g of a 20% aqueous sulfuric acid solution were added and neutralized by stirring. The hexane layer was washed with ion-exchanged water and distilled to obtain a mixture containing the component (b-3) at 60% by weight. <Evaluation of deodorant performance> Cutting board (23.0 × 41.
0 x 1.5 cm, material: polyethylene) After finely chopping 10 g of sardine fillet, solids were removed,
Rinse the cutting board surface lightly with water. 3 g of detergent shown in Table 1 and water (hardness: 3.5 DH, Mg ion / Ca ion = 1/3)
Sponge impregnated with 27 g of water
Using 0.5 × 7.5 × 4.0 cm, material: polyurethane foam), the surface of the cutting board was evenly hand-washed for 3 minutes. Panels of 10 males and 5 females in their 30s (five each) smelled the smell of the cutting board after washing, and two points when no odor was detected and one point when odor was detected. ○ The average score of 10 people is 1.75 points or more.
The deodorizing performance was evaluated as “Poor” when the score was equal to or more than 1.75 points, and “X” when the score was less than 1.5 points. [Table 1] The deodorant cleaning agent of the present invention can be used for tableware, cutting boards,
Excellent detergency and deodorant performance against food odors attached to objects to be cleaned such as kitchen knives, grilled fish, sponges and the like.

───────────────────────────────────────────────────── フロントページの続き (56)参考文献 特開2000−103764(JP,A) 特開 平2−84496(JP,A) 特開2000−192082(JP,A) 特開 昭57−117599(JP,A) (58)調査した分野(Int.Cl.7,DB名) C11D 1/68 C11D 1/04 C11D 1/10 C11D 3/20 C11D 3/50 CAPLUS(STN) REGISTRY(STN)──────────────────────────────────────────────────続 き Continuation of the front page (56) References JP-A-2000-103764 (JP, A) JP-A-2-84496 (JP, A) JP-A-2000-192082 (JP, A) JP-A-57-117599 ( JP, A) (58) Fields investigated (Int. Cl. 7 , DB name) C11D 1/68 C11D 1/04 C11D 1/10 C11D 3/20 C11D 3/50 CAPLUS (STN) REGISTRY (STN)

Claims (1)

(57)【特許請求の範囲】 【請求項1】 下記(a)、(b)、(c)成分及び水
を含有し、(b)成分と(c)成分の合計量が0.5〜
20重量%で、かつ重量比が(b)/(c)=10/9
0〜90/10である消臭洗浄剤。 (a)アルキルグリコシド 0.1〜40重量% (b)下記一般式(4)又は(6)で表されるポリカル
ボン酸型界面活性剤 【化1】 [式中、R は炭素数8〜20のアルキル基又はアルケ
ニル基で、HLBがカルボン酸の状態で4〜15、及び
酸の状態として重量分当たりの酸価が300〜600m
gKOH/gの範囲を満足するように選ばれる。HLB
は、デービス法(界面活性剤 物性・応用・化学生態
学,北原文雄ら著,講談社サイエンティフィック 第7
刷発行,P24〜27に記載の方法)により測定され
る。酸価は、酸の状態で0 . 5gをトルエン/エタノー
ル(容量比50/50、フェノールフタレイン0 . 5重
量%添加)溶媒50mgに溶解させ、0.1NのKOH
で滴定し、フェノールフタレインが着色した時点を終点
とし、要したKOHの量をmgで表した数値である。] (c)1以上のカルボキシル基を有する炭素数が3〜7
の化合物
(57) [Claims 1] It contains the following components (a), (b) and (c) and water, and the total amount of the components (b) and (c) is 0.5 to 0.5.
20% by weight and weight ratio (b) / (c) = 10/9
0 to 90/10 deodorant detergent. (A) Alkyl glycoside 0.1 to 40% by weight (b) Polycarboxylic acid type surfactant represented by the following general formula (4) or (6) Wherein R 8 is an alkyl group having 8 to 20 carbon atoms or an alk
A carbonyl group, wherein the HLB is in the form of a carboxylic acid, 4 to 15, and
The acid value is 300-600m per weight minute as the acid state
It is selected so as to satisfy the range of gKOH / g. HLB
Is the Davis method (surfactant Physical properties / application / chemical ecology
Gaku, Fumio Kitahara et al., Kodansha Scientific Seventh
Printing issuance, the method described on pages 24 to 27)
You. Acid value, 0 in the form of an acid. 5 g of toluene / ethanol
Le (volume ratio of 50/50, phenolphthalein 0.5-fold
Dissolved in 50 mg of solvent and 0.1N KOH
At the point when phenolphthalein is colored
And the required amount of KOH is a numerical value expressed in mg. (C) 3 to 7 carbon atoms having one or more carboxyl groups
Compound of
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