JP2005029754A - Aqueous liquid composition - Google Patents

Abstract

<P>PROBLEM TO BE SOLVED: To provide an aqueous liquid composition, capable of removing attached dyestuff easily even if its stock solution is attached on a hard surface without being diluted and dried. <P>SOLUTION: This aqueous liquid solution contains (a) 0.1-20 mass% polymer containing 10-100 mol.% monomer unit having a tert-amino group and/or quaternary ammonium group, (b) 0.001-1 mass% acid dyestuff and water. <P>COPYRIGHT: (C)2005,JPO&NCIPI

Description

  The present invention relates to an aqueous liquid composition containing a polymer compound having a tertiary amino group and / or a quaternary ammonium group, and an acid dye, and is particularly installed in the upper part of the tank of a flush toilet or placed in the tank of a flush toilet. It is related with the aqueous | water-based liquid composition which can be used for the washing | cleaning agent for toilets (henceforth a cleaning agent for stationary toilets etc.) etc. which are automatically introduce | transduced into a toilet every flash | flush by this method.

  It is known to use a dye from a aesthetic point of view for a water storage tank stationary toilet cleaner. Patent Document 1 discloses a fragrance cleaning composition for flush toilets containing a colorant. The detailed description of the publication includes Blue No. 1 (CIAcid Blue 9) and Blue No. 2 (CIAcid Blue 74). And blue acid dyes such as Blue 202 (CIAcid Blue 5). Patent Document 2 discloses a technique for a vehicle toilet sewage treatment deodorant containing a pigment for food additives such as Blue No. 1, a pigment selected from a triphenylmethane pigment and an oxazine pigment. Further, as dyes that can be used for toilet cleaners or deodorant fragrances, those described in the detailed description of the inventions of Patent Documents 3 to 6 are known. These washing agents for water tank stationary type toilets containing dyes are generally in solid form. For liquid types, for example, a composition containing a large amount of dyes in the detailed description of the invention of Patent Document 7 Things are listed. Patent Document 8 discloses a composition that does not stain even if it adheres to a hand or finger containing an acidic dye and a cationic surfactant.

On the other hand, a technique for applying a polymer compound containing a quaternary ammonium group to a toilet cleaner is already known. Patent Document 9 discloses an antifouling detergent composition for toilets in which an anionic surfactant and a quaternary ammonium compound are used in combination. Patent Documents 10 to 12 disclose techniques of a quaternary ammonium type surfactant and a polymer having a tertiary amino group or a quaternary ammonium group.
JP-A-6-330096 JP-A-5-138153 JP-A-8-104898 JP-A-8-81695 JP 2000-144177 A JP-A-10-140198 JP-A-4-345699 Japanese Patent Laid-Open No. 10-155858 JP-A-9-169995 Japanese Patent Laid-Open No. 2002-60786 JP 2002-146397 A Japanese Patent Laid-Open No. 2002-60784

  However, liquid-type compositions such as Patent Document 7 are not diluted and directly adhere to hard surfaces such as toilet water storage tanks, toilet tiles, toilets, and the like. There is a problem that it cannot be removed and the appearance is remarkably impaired. Although the composition of Patent Document 8 does not stain even if it adheres to the hand or finger, the dye cannot be easily removed when the undiluted solution adheres directly to the hard surface and is dried.

  Moreover, although the technique of patent documents 9-12 is the dirt washing | cleaning effect or antifouling effect of a toilet, and although it is described in this gazette detailed description that a dye can be contained arbitrarily, a stock solution is hard without being diluted. When it adheres to the surface or when a diluent with a concentration higher than the designed working concentration adheres (such as when the stock solution is discharged in a concentrated state due to water droplets attached at the initial stage of dilution or near the container discharge part) It is not possible to suggest any means for solving the coloring problem.

  An object of the present invention is to provide an aqueous liquid composition that can easily remove an attached dye even if the stock solution is directly diluted and adhered to a hard surface and dried.

  The present invention provides (a) a polymer compound [hereinafter referred to as component (a)] containing 10 to 100 mol% of a monomer unit having a tertiary amino group and / or quaternary ammonium group in the molecule. The present invention relates to an aqueous liquid composition containing 20% by mass, (b) an acidic dye (hereinafter referred to as component (b)) in an amount of 0.001 to 1% by mass, and water.

  According to the present invention, an aqueous liquid composition can be obtained that can easily remove attached dye even when a stock solution or a diluted solution that is thicker than the designed use concentration adheres to a hard surface and is dried. The aqueous liquid composition of the present invention can be suitably used for a liquid type storage tank stationary toilet cleaning agent and the like by filling an appropriate container.

<(A) component>
The component (a) of the present invention is a polymer compound containing 10 to 100 mol% of a monomer unit having a quaternary ammonium group and / or a tertiary amino group (hereinafter referred to as monomer unit A). The weight average molecular weight is preferably 1,000 to 6,000,000, more preferably 2,000 to 2,000,000, and particularly preferably 5,000 to 2,000,000. The molecular weight can be measured by gel permeation chromatography using polyethylene glycol as a standard substance.

Monomer unit A is a monomer that polymerizes a monomer (hereinafter referred to as monomer A) containing a quaternary ammonium group (may be plural) or contains a tertiary amino group (may be plural). A monomer unit obtained by polymerizing (hereinafter referred to as monomer A ′) may be used, or a tertiary amino group may be quaternized by conversion to quaternary ammonium.
Preferable examples of the monomer A having a quaternary ammonium group include compounds represented by the following general formula (1).

^{Wherein, R 1a, R 1b, R} 1c are each independently hydrogen atom, a hydroxyl group or an alkyl group having 1 to 3 carbon atoms. B is an alkylene group having 1 to 12 carbon ^{atoms, -COOR 1g -, - CONHR 1g} -, - OCOR 1g -, - R 1h -OCO-R 1g - a group selected from. Here, R ^1g and R ^1h are each independently an alkylene group having 1 to 5 carbon atoms. R ^1d is an alkyl group having 1 to 3 carbon atoms or a hydroxyalkyl group, or (R ^1a ) (R ^1b ) C═C (R ^1c ) —B—. R ^1e is an alkyl group having 1 to 3 carbon atoms, a hydroxyalkyl group, or a benzyl group, and R ^1f is an alkyl group having 1 to 10 carbon atoms that may be substituted with a hydroxy group, a carboxyl group, a sulfonic acid group, or a sulfate group. When it is an alkyl group or a benzyl group and R ^1f is an alkyl group, a hydroxyalkyl group or a benzyl group, X ⁻ represents an anion. In addition, when R ^1f contains a carboxyl group, a sulfonic acid group, or a sulfate group, X ⁻ does not exist, and these groups in R ^1f become anions. Examples of the anion of X ⁻ include a halogen ion, a sulfate ion, an alkyl sulfate ester ion having 1 to 3 carbon atoms, an aromatic sulfonate ion optionally substituted with an alkyl group having 1 to 3 carbon atoms, and a hydroxy ion. be able to. ]

  Among these, acryloyl (or methacryloyl) aminoalkyl (C1 to C5) -N, N, N-trialkyl (C1 to C3) quaternary ammonium salt, acryloyl (or methacryloyl) oxyalkyl (C1 to C1) 5) -N, N, N-trialkyl (C1-3) quaternary ammonium salt, N- (ω-alkenyl (C3-10))-N, N, N-trialkyl (C1) -3) Quaternary ammonium salt, N, N-di (ω-alkenyl (3 to 10 carbon atoms))-N, N-dialkyl (1 to 3 carbon atoms) quaternary ammonium salt is preferred, especially diallyldimethylammonium salt Is good.

  Preferable examples of the tertiary amino group monomer A ′ include compounds of the following general formula (1-a).

  Among these, N, N-dialkyl (C1-3) aminoalkyl (C1-5) acrylate (or methacrylate), N, N-dialkyl (C1-3) aminoalkyl (C1-5) ) Acrylamide, N, N-di (ω-alkenyl (3 to 10 carbon atoms))-N-methylamine are preferred, and diallylmethylamine is particularly preferred.

  In the case of quaternizing the monomer A ′, methyl chloride, methyl bromide, benzyl chloride, dimethyl sulfate, diethyl sulfate, monochloroacetic acid or a salt thereof, chlorosulfonic acid or a salt thereof, 3-chloro-2- It is preferable to carry out using hydroxypropanesulfonic acid or a salt thereof, ethylene oxide, propylene oxide, or glycidyl ether. In addition, when using ethylene oxide, propylene oxide, and glycidyl ether, it is preferable to make it react, after neutralizing a monomer unit previously with a sulfuric acid, hydrochloric acid, a C1-C12 carboxylic acid, allylsulfonic acid, etc.

  The component (a) of the present invention includes not only a polymer composed of monomer unit A (or monomer unit A ′, which may be plural types), but also monomer unit A (or monomer unit A ′, plural types). And a polymer composed of another monomer unit (hereinafter referred to as monomer unit B). In this case, the arrangement pattern of the monomer unit A and the monomer unit B (may be plural types) may be any of block, alternating, period, statistics (including random), and graft type.

  A polymer composed of the monomer unit A (and / or the monomer unit A ′) and the monomer unit B can be obtained, for example, by copolymerizing respective precursor monomers. In this case, the monomer unit B is preferably a monomer unit derived from a monomer selected from the following monomer groups (i) to (v), and the monomer unit derived from the monomer described in (i) to (iii) or (v): The monomer unit derived from the monomer (i), (ii) or (v) is most preferable from the viewpoint of the antifouling effect.

(I) Acrylic acid or its salt, methacrylic acid or its salt, maleic acid or its salt, maleic anhydride, styrene sulfonate, sulfopropyl methacrylate, 2-acrylamido-2-methylpropane sulfonic acid or its salt, phosphoric acid Anionic group-containing compound selected from mono-ω-methacryloyloxyalkyl (C 1-12)

(Ii) Acrylamide, N, N-dimethylaminopropylacrylic acid (or methacrylic acid) amide, N, N-dimethylacrylic (or methacrylic) amide, N, N-dimethylaminoethylacrylic acid (or methacrylic acid) amide, N , N-dimethylaminoethylacrylic acid (or methacrylic acid) amide, N-vinyl-2-caprolactam, N-vinyl-2-pyrrolidone-containing compound

(Iii) Acrylic acid (or methacrylic acid) alkyl (1 to 5 carbon atoms), acrylic acid (or methacrylic acid) 2-hydroxyethyl, acrylic acid (or methacrylic acid) -N, N-dimethylaminoalkyl (1 carbon atom) -5), ester group-containing compound selected from vinyl acetate

(Iv) Ethylene, propylene, N-butylene, isobutylene, N-pentene, isoprene, 2-methyl-1-butene, N-hexene, 2-methyl-1-pentene, 3-methyl-1-pentene, 4-methyl -1-pentene, 2-ethyl-1-butene, styrene, vinyltoluene, α-methylstyrene, allylamine, N, N-diallylamine, N, N-diallyl-N-alkyl (C 1-5) amine, ethylene oxide , Propylene oxide, 2-vinylpyridine, a compound selected from 4-vinylpyridine

(V) Sulfur dioxide

  In addition to the synthesis method by copolymerization as described above, the polymer having the monomer unit A and the monomer unit B is preferably a monomer containing the monomer unit A in addition to the monomer (i) to (v), particularly preferably the above (i). , (Ii) may be obtained by graft polymerization, or may be obtained by graft polymerization of the monomer of the general formula (1) to the polymer containing the monomers (i) to (v). , After graft polymerization of the monomer of the general formula (1-a) to the polymer containing the monomers (i) to (v), particularly preferably the polymer containing the monomers (i) and (ii), This may be quaternized.

  The most preferable monomer unit B of the present invention is derived from a monomer having one or more groups selected from a carboxylic acid group and a sulfonic acid group [but not having a quaternary ammonium group], that is, the monomer of the above (i). Monomer unit (hereinafter referred to as monomer unit B ′).

The polymer constituting the component (a) of the present invention may be obtained by any polymerization method, but a radical polymerization method is particularly preferred, and this can be carried out in a bulk, solution, or emulsion system. Radical polymerization may be initiated by heating, but as an initiator, 2,2′-azobis (2-amidinopropane) dihydrochloride, 2,2′-azobis (N, N-dimethyleneisobutylamidine) Azo initiators such as dihydrochloride, hydrogen peroxide and organic peroxides such as benzoyl peroxide, t-butyl hydroperoxide, cumene hydroperoxide, methyl ethyl ketone peroxide, perbenzoic acid, sodium persulfate, Existing radical initiators such as persulfates such as potassium persulfate and ammonium persulfate, and redox initiators such as hydrogen peroxide-Fe ³⁺ may be used, and in the presence or absence of a photosensitizer. The polymerization may be initiated by light irradiation or radiation irradiation.

  The component (a) of the present invention may be a single polymer of monomer units A and a mixture of plural kinds of polymers selected from copolymers of monomer units A and B.

  In the component (a) of the present invention, a more preferable configuration is that the sum of the monomer unit A (and / or the monomer unit A ′) and the monomer unit B ′ is 50 to 100 mol% based on the total monomer units, Most preferably, the molar ratio of monomer unit A (and / or monomer unit A ′), B ′ is [monomer unit A (and / or monomer unit A ′)] / [monomer unit A (and / or monomer unit A ′). ) + Monomer unit B ′] = 0.3-0.95, in particular 0.5-0.95.

<(B) component>
The component (b) of the present invention is an acid dye, and has at least one sulfonic acid group in the molecule, preferably 1 to 5, more preferably from the viewpoint of obtaining a preferable color tone and stability in the composition. One to three acid dyes are preferred. Specifically, those having a sulfonic acid group are preferable among the dyes selected from the acid dyes described in “Dye Handbook” (edited by the Society for Synthetic Organic Chemistry, published by Maruzen Co., Ltd.), and the following compounds can be exemplified.

  Specifically, CIAcid Yellow 1, CIAcid Yellow 7, CIAcid Yellow 11, CIAcid Yellow 17, CIAcid Yellow 23, CIAcid Yellow 25, CIAcid Yellow 29, CIAcid Yellow 36, CIAcid Yellow 38, CI Acid Yellow 40, CIAcid Yellow 42, CIAcid Yellow 44, CIAcid Yellow 76, CIAcid Yellow 98, CIAcid Yellow 99, CIFOd Yellow 3, CIAcid Orange 1, CIAcid Orange 7, CIAcid Orange 8, CI Acid Orange 10, CIAcid Orange 10, CIAcid Orange 19, CIAcid Orange 20, CIAcid Orange 24, CIAcid Orange 28, CIAcid Orange 33, CIAcid Orange 41, CIAcid Orange 45, CIAcid Orange 51, CI Acid Orange 56, CIAcid Orange 74, CIAcid Red 1, CIAcid Red 6, CIAcid Red 8, CIAcid Red 9, CIAcid Red 13, CIAcid Red 14, CIAcid Red 18, CIAcid Red 26, CI Acid Red 27, CIAcid Red 32, CIAcid Red 35, CIAcid Red 37, CIAcid Red 42, CIAcid Red 52, CIAcid Red 80, CIAcid Red 82, CIAcid Red 83, CIAcid Red 85, CI Acid Red 88, C. I. Acid Red 89, CIAcid Red 97, CIAcid Red 106, CIAcid Red 111, CIAcid Red 114, CIAcid Red 115, CIAcid Red 133, CIAcid Red 134, CIAcid Red 145, CIAcid Red 154 , CIAcid Red 155, CIAcid Red 158, CIAcid Red 180, CIAcid Red 183, CIAcid Red 184, CIAcid Red 186, CIAcid Red 198, CIAcid Red 249, CIAcid Red 265, CIAcid Red 1 , CIAcid Blue 7, CIAcid Blue 9, CIAcid Blue 15, CIAcid Blue 22, CIAcid Blue 23, CIAcid Blue 25, CIAcid Blue 27, CIAcid Blue 29, CIAcid Blue 40, CIAcid Blue 41 , CIAcid Blue 43, CIAcid Blue 45, CIAcid Blue 59, CIAcid Blue 62, CIAcid Blue 74, CIAcid Blue 78, CIAcid Blue 80, CIAcid Blue 82, CIAcid Blue 83, CIAcid Blue 90 , CIAcid Blue 92, CIAcid Blue 93, CIAcid Blue 100, CIAcid Blue 102, CIAcid Blue 103, CIAcid Blue 104, CIAcid Blue 112, CIAcid Blue 113, CIAcid Blue 117, CIAcid Blue 120 , CIAcid Blue 126, CIAcid Blue 127, CIAcid Blue 138, C.I. Acid Blue 158, C.I. Acid Blue 16 are listed.

  In the present invention, CIAcid Yellow 23, CIFOd Yellow 3, CIAcid Red 27, CIAcid Red 18, CIAcid Red 52, CIAcid Red 49, CIAcid Blue 9, CIAcid Blue are particularly preferred in terms of liquid phase stability. One or more selected from 74, CIAcid Blue 112, and CIAcid Green 5 are preferable. Among these, C.I.Acid Blue 9, C.I.Acid Blue 112, and C.I.Acid Blue 74 are preferable, and C.I.Acid Blue 112 is particularly preferable from the viewpoint of fading.

<Aqueous liquid composition>
The aqueous liquid composition of the present invention contains (a) component in an amount of 0.1 to 20% by mass, preferably 0.5 to 15% by mass, more preferably 1 to 10% by mass, and particularly preferably 2 to 8% by mass. . Moreover, (b) component is 0.001-1 mass%, Preferably it is 0.001-0.3 mass%, More preferably, it is 0.003-0.1 mass%, Most preferably, it is 0.005-0.05 mass. %contains. The mass ratio of component (b) / component (a) is preferably 0.0001 to 0.1, more preferably 0.0005 to 0.05, and particularly preferably 0 from the viewpoint of dye adhesion prevention on the hard surface. 0.001 to 0.03.

  The aqueous liquid composition of the present invention is in the form of a liquid composition in which the components (a) and (b) are dissolved or dispersed in water, and the water content is preferably 20 to 80% by mass, particularly preferably. 30 to 60% by mass.

  Further, the pH of the aqueous liquid composition of the present invention at 20 ° C. is preferably 2 to 12, more preferably 3 to 11, and particularly preferably 5 to 9. As pH adjusters, acid agents such as inorganic acids such as hydrochloric acid and sulfuric acid, organic acids such as citric acid, succinic acid, malic acid, fumaric acid, tartaric acid, malonic acid, maleic acid, sodium hydroxide and potassium hydroxide, It is preferable to use alkali agents such as sodium carbonate and potassium carbonate alone or in combination, such as ammonia and derivatives thereof, amine salts such as monoethanolamine, diethanolamine, and triethanolamine, and particularly selected from hydrochloric acid, sulfuric acid, and citric acid. It is preferable to use an acid selected from the group consisting of acid and sodium hydroxide, potassium hydroxide, or an alkali agent selected from the above amine compounds.

  The effect of the present invention is basically obtained by using the components (a) and (b) in combination, and is particularly suitable for application to a liquid toilet cleaner for standing water tanks. Further, when the liquid composition of the present invention is applied to such a toilet cleaner, a fragrance for the purpose of a preferred fragrance or deodorant, a surfactant for the purpose of cleaning and foaming, and antibacterial An agent can be used in combination.

  As a fragrance | flavor, a single fragrance | flavor component may be used and it can also be used as a fragrance | flavor composition which contains several fragrance | flavor components by a specific ratio. Perfume ingredients include “Chemicals of Perfume” (Ryoichi Akahoshi, edited by the Chemical Society of Japan, Industrial Chemistry Series, issued on September 16, 1983) and “Synthetic Perfume Chemistry and Product Knowledge” (Genji Into, Chemical Industry Daily) , Issued on March 6, 1996) or "Basic knowledge of perfumes and fragrances" (by Nakajima Motoki, Sangyo Tosho Co., Ltd., issued on June 21, 1995).

  Specific examples include hydrocarbon flavors, alcohol flavors, ether flavors, aldehyde flavors, ketone flavors, ester flavors, lactone flavors, cyclic ketone flavors, and nitrogen-containing flavors.

(A-1): Hydrocarbon-based fragrance α-pinene, β-pinene, camphene, myrcene, limonene, terpineol, terpinolene, osymene, γ-terpinene, α-ferrandylene, p-cymene, β-caryophyllene, β-farnesene 1,3,5-undecatriene, diphenylmethane

(A-2): Alcohol-based perfume trans-2-hexenol, cis-3-hexenol, 3-octanol, 1-octen-3-ol, 2,6-dimethyl-2-heptanol, 9-decenol, 4-methyl -3-decen-5-ol, 10-undecenol, trans-2-cis-6-nonadienol, linalool, geraniol, nerol, citronellol, rosinol, myrsenol, lavandurol, tetrahydrogeraniol, tetrahydrolinalool, hydroxycitronellol, dihydromil Senol, alo-osimenol, terpineol, turpinen-4-ol, l-menthol, borneol, isopulegol, nopol, farnesol, nerolidol, bisabolol, cedrol, patchouli alcohol, vetivero 2,4-dimethyl-3-cyclohexene-1-methanol, 4-isopropylcyclohexanol, 4-isopropylcyclohexanemethanol 1- (4-isopropylcyclohexyl) -ethanol, 2,2-dimethyl-3- (3- Methylphenyl) -propanol, pt-butylcyclohexanol, ot-butylcyclohexanol, ambrinol, benzyl alcohol, phenylethyl alcohol, phenoxyethanol, styryl alcohol, anis alcohol, cinnamic alcohol, phenylpropyl alcohol, dimethyl Benzyl carbinol, phenylethylmethylethyl carbinol, 3-methyl-5-phenylpentanol, thymol, carvacrol, orcinol monomethyl ether, eugeno Le, isoeugenol, santalol, isobornyl cyclohexanol, Sandaroa, Bagudanoru, sandal Mai Sol core, Buramanoru, Ebanoru, poly San tall, 2-ethoxy-4-methoxy-methylphenol

(A-3); ether-based fragrance nerol oxide, miloxide, 1,8-cineol, rose oxide, limetolfuran, linalool oxide, butyldimethyldihydropyran, acetoxyamyltetrahydropyran, cedrylmethyl ether, methoxycyclododecane , 1-methyl-1-methoxycyclododecane, ethoxymethylcyclododecyl ether, tricyclodecenyl methyl ether, rubofix, cedroxide, ambroxan, glycalva, boisiris, anisole, dimethylhydroquinone, paracresyl methyl ether, acetanisole , Anethole, dihydroanethole, estragole, diphenyl oxide, methyl eugenol, methyl isoeugenol, benzyl isoeugenol, Phenylethyl isoamyl ether, β-naphthyl methyl ether, β-naphthyl ethyl ether, β-naphthyl isobutyl ether, 2,4-dimethyl-4-phenyltetrahydrofuran, galaxide

(A-4) Aldehyde fragrances Hexylaldehyde, heptylaldehyde, octylaldehyde, nonylaldehyde, decylaldehyde, undecylaldehyde, dodecylaldehyde, tridecylaldehyde, trimethylhexylaldehyde, methyloctylacetaldehyde, methylnonylacetaldehyde, trans-2- Hexenal, cis-4-heptenal, 2,6-nonadienol, cis-4-decenal, undecylene aldehyde, trans-2-dodecenal, trimethylundecenal, 2,6,10-trimethyl-5,9-undecadienal , Citral, citronellal, hydroxycitronellal, perilaldehyde, methoxydihydrocitronellal, citronellyloxyacetaldehyde, isocyclocitral , Centenal, Lilal, Bernaldehyde, Dupical, Maceart, Boronal, Setneral, Phenylacetaldehyde, Phenylpropylaldehyde, Cynamic aldehyde, α-Amylcinnamic aldehyde, α-Hexylcinnamic aldehyde, Hydratropic aldehyde, Anisaldehyde, p -Methylphenylacetaldehyde, cuminaldehyde, cyclamenaldehyde, 3- (pt-butylphenyl) -propylaldehyde, p-ethyl-2,2-dimethylhydrocinnamaldehyde, 2-methyl-3- (p-methoxyphenyl) -Propyl aldehyde, pt-butyl-α-methylhydrocinnamic aldehyde, salicylaldehyde, heliotropin, helional, vanillin, ethyl vanillin, Ruvanillin, 10-undecenal, lyial, 1,2,3,4,5,6,7,8-octahydro-8,8-dimethyl-2-naphthaldehyde, 1-methyl-4- (4-methyl-3- Pentenyl) -3-cyclohexene-1-carboxaldehyde, nonanal, 2,4-dimethyl-3-cyclohexene-1-carboxaldehyde, 3,5-dimethyl-3-cyclohexene-1-carboxaldehyde (note that 2,4 -A mixture of dimethyl-3-cyclohexene-1-carboxaldehyde and 3,5-dimethyl-3-cyclohexene-1-carboxaldehyde is commercially available as LIGUSTRAL from QUEST), benzaldehyde, mylacaldehyde

(A-5); ketone-based fragrance acetoin, diacetyl, methyl amyl ketone, ethyl amyl ketone, methyl hexyl ketone, methyl nonyl ketone, methyl heptyl ketone, acetyl diisoamylene, camphor, carvone, menthone, d-pregon, piperiton, Fengchon, geranylacetone, cedryl methyl ketone, nootkatone, α-ionone, β-ionone, methylionone, α-n-methylionone, β-n-methylionone, α-isomethylionone, β-isomethylionone, allylionone , Α-iron, β-iron, γ-iron, α-damascon, β-damascon, δ-damascon, damaserin, α-dynascon, β-dynascon, maltol, ethyl maltol, 2,5-dimethyl-4-hydroxyfuranone , Sugar Lac , P-t-butylcyclohexanone, amylcyclopentanone, heptylcyclopentanone, dihydrojasmon, cis-jasmon, florex, plicatone, 4-cyclohexyl-4-methyl-2-pentanone, p-menten-6-ylpropanone, Acetophenone, p-methylacetophenone, benzylacetone, callone, raspberry ketone, anisylacetone, methylnaphthylketone, benzophenone

(A-6); ester-based fragrance ethyl formate, cis-3-hexenyl formate, linalyl formate, citronellyl formate, geranyl formate, benzyl formate, phenylethyl formate, ethyl acetate, butyl acetate, isoamyl acetate, methyl cyclopentylidene acetate, Hexyl acetate, cis-3-hexenyl acetate, trans-2-hexenyl acetate, isononyl acetate, citronellyl acetate, lavandulyl acetate, geranyl acetate, linalyl acetate, mircenyl acetate, tarpinyl acetate, menthin acetate, menthanyl acetate, nopyru acetate, n-acetate Bornyl, isobornyl acetate, pt-butylcyclohexyl acetate, o-t-butylcyclohexyl acetate, tricyclodecenyl acetate, 2,4-dimethyl-3-cyclohexene-1-methanyl acetate, benzyl acetate, phenylethyl acetate, Stylacetate Laryl, cinnamyl acetate, anisyl acetate, paracresyl acetate, heliotropyl acetate, acetyl eugenol, acetyl isoeugenol, guayl acetate, cedolyl acetate, vetiberyl acetate, ethyl propionate, isoamyl propionate, citronellyl propionate, geranyl propionate, linalyl propionate, Terpinyl propionate, benzyl propionate, cinnamyl propionate, allyl cyclohexylpropionate, tricyclodecenyl propionate, ethyl butyrate, ethyl 2-methylbutyrate, butyl butyrate, isoamyl butyrate, hexyl butyrate, linalyl butyrate, geranyl butyrate, butyric acid Citronellyl, benzyl butyrate, cis-3-hexenyl isobutyrate, citronellyl isobutyrate, geranyl isobutyrate, linalyl isobutyrate, benzyl isobutyrate, isobutyrate Phenylethyl, tricyclodecenyl isobutyrate, ethyl isovalerate, propyl valerate, citronellyl isovalerate, geranyl isovalerate, benzyl isovalerate, cinnamyl isovalerate, phenylethyl isovalerate, ethyl caproate, Allyl caproate, ethyl enanthate, allyl enanthate, ethyl caprate, citronellyl tiglate, methyl benzoate, ethyl benzoate, isobutyl benzoate, isoamyl benzoate, geranyl benzoate, linalyl benzoate, benzyl benzoate, benzoic acid Phenyl ethyl, methyl phenyl acetate, ethyl phenyl acetate, isobutyl phenyl acetate, isoamyl phenyl acetate, geranyl phenyl acetate, benzyl phenyl acetate, phenyl ethyl phenyl acetate, p-cresyl phenyl acetate, methyl cinnamate, ethyl cinnamate Benzyl cinnamate, cinnamyl cinnamate, phenylethyl cinnamate, methyl salicylate, ethyl salicylate, isobutyl salicylate, amyl salicylate, hexyl salicylate, cis-3-hexenyl salicylate, benzyl salicylate, phenylethyl salicylate, methyl jasmonate, dihydrojasmonic acid Methyl, frutate, allyl 2-pentyloxyglycolate, ethyl 3-methyl-3-phenylglycidate, ethyl 2-pentanoate, 4-acetoxy-3-amyltetrahydropyran

(A-7): Lactone fragrance, cyclic ketone fragrance γ-octalactone, γ-nonalactone, γ-decalactone, γ-undecalactone, δ-decalactone, coumarin, dihydrocoumarin, jasmonolactone, jasmine lactone, muscone , Civeton, cyclopentadecanone, cyclohexadecenone, cyclopentadecanolide, 12-ketocyclopentadecanolide, cyclohexadecanolide, cyclixadecenolide, 12-oxa-16-hexadecanolide, 11-oxa -16-hexadecanolide, 10-oxa-16-hexadecanolide, ethylan brushate, ethylenedodecanedioate

(A-8): Nitrogen-containing fragrance 6-sec-butylquinoline, 5-methyl-3-heptanone oxime, citronellylnitrile

  The names of the above fragrance ingredients basically followed the description in “Basic knowledge of fragrances and fragrances” (written by Motoki Nakajima, Sangyo Tosho Co., Ltd., issued on June 21, 1995).

  When the aqueous liquid composition of the present invention is applied to a toilet cleaner, the fragrance composition obtained by combining a single fragrance component or a plurality of components is preferably 0.1 to 10% by mass in the aqueous liquid composition. More preferably, the content is 0.2 to 5% by mass, and particularly preferably 0.5 to 3% by mass.

  Surfactants that can be used in the aqueous liquid composition of the present invention are nonionic surfactants, amphoteric surfactants, and cationic surfactants, and anionic surfactants may hinder the effects of the present invention. Therefore, it is suitable to refrain from use, and when used, the anionic surfactant is preferably 50 parts by mass or less, more preferably 30 parts by mass or less, particularly 100 parts by mass of component (a). Preferably, it should be 10 parts by mass or less.

  As a preferable surfactant when the aqueous liquid composition of the present invention is applied to a toilet cleaner, a compound of the following general formula (2) is preferable from the viewpoint of foaming power and cleaning effect.

R ^2a − (OR ^2b ) _e G _f (2)
[Wherein, R ^2a is a linear alkyl group having 8 to 16, preferably 10 to 16, particularly preferably 10 to 14 carbon atoms, and R ^2b is an alkylene group having 2 to 4 carbon atoms, preferably ethylene group or propylene. A group, particularly an ethylene group, G is a residue derived from a reducing sugar, e is an average value of 0-6, f is an average value of 1-10, preferably 1-5, particularly preferably 1-2. Indicates. ]

  In the compound of the general formula (2), G is a residue derived from a reducing sugar, and the starting reducing sugar may be either aldose or ketose, and a triose having 3 to 6 carbon atoms. , Tetrose, pentose, hexose. Specific examples of aldose include apiose, arabinose, galactose, glucose, lyxose, mannose, aldose, idose, talose and xylose, and examples of ketose include fructose. In the present invention, among these, aldopentose or aldohexose having 5 or 6 carbon atoms is particularly preferred, and glucose is most preferred. As the reducing sugar of G, the above monosaccharide is preferable, but an oligosaccharide obtained by condensing 2 to 5, preferably 2 or 3 of these monosaccharides may be used. Further, a mixture of monosaccharide and oligosaccharide may be used. In this case, the average degree of condensation is 1 to 5, preferably 1 to 3, particularly preferably 1 to 2, and most preferably 1 to 1.5. preferable.

The compound of the general formula (2) can be easily synthesized by subjecting R ^2a — (OR ^2b ) _e —OH and a reducing sugar to an acetalization reaction or a ketalization reaction using an acid catalyst. In the case of an acetalization reaction, these may have a hemiacetal structure or a normal acetal structure.

  When the aqueous liquid composition of the present invention is applied to a toilet cleaner, the compound represented by the general formula (2) is preferably 5 to 40% by mass, more preferably 10 to 30% by mass in the composition, Particularly preferably, 12 to 24% by mass is used.

  The cationic surfactant is preferably contained because it has detergency and foamability and can impart an antibacterial effect to the composition of the present invention. In the present invention, the most preferred cationic surfactants include the following.

  In the present invention, these cationic surfactants are preferably contained in the composition in an amount of 0.1 to 15% by mass, more preferably 0.5 to 10% by mass, and particularly preferably 1 to 8% by mass.

  For the purpose of imparting an antibacterial effect, an antibacterial compound other than the cationic surfactant may be contained. The antibacterial compound is a compound in which an antibacterial test is carried out by a method of JIS L 1902 “Textile antibacterial test method” using a cloth in which 1% by mass of the compound is uniformly adhered to a cotton gold width # 2003, and a blocking band is observed. It is. Such compounds are described in pages 501 to 564 of “Science of Cosmetics, Pharmaceutical Preservatives and Bactericides” (by Koichi Yoshimura and Hirofumi Takikawa, issued by Fragrance Journal, April 10, 1990). You can choose from.

  Preferred antibacterial compounds include 2- (4-thiocyanomethylthio) benzimidazole, polylysine, polyhexamethylene biguanilide and chlorhexidine glucuronate, triclosan, bis- (2-pyridylthio-1-oxide) zinc, 2,4, Selected from 5,6-tetrachloroisophthalonitrile, trichlorocarbanilide, 8-oxyquinoline, dehydroacetic acid, benzoates, chlorocresols, chlorothymol, chlorophene, dichlorophen, bromochlorophene, hexachlorophene One or more. Triclosan is particularly preferred from the viewpoint of antibacterial effect. Triclosans described in JP-A-11-189975 are also good, and specifically, dichlorohydroxydiphenyl ether and monochlorohydroxydiphenyl ether are preferable.

  In the present invention, an antibacterial agent other than the cationic surfactant is preferably added in the composition in an amount of 0.001 to 8% by mass, more preferably 0.001 to 5% by mass, and particularly preferably 0.005 to 3% by mass.

  The aqueous liquid composition of the present invention preferably contains a water-soluble organic solvent from the viewpoint of storage stability. Furthermore, for the purpose of stability, a hydrotrope agent, a metal sequestering agent, a normal dispersant, an antiseptic, and the like can be added within the range not impairing the effects of the present invention for the purpose of removing a deposition component derived from calcium.

10% by mass of Calcoat Marcoat 280 (diallyldimethylammonium chloride and acrylic acid copolymer (64:36, molar ratio), molecular weight 1.7 million), alkyl glucoside (carbon number of alkyl group: 12, glucose average condensation degree: 1) 5) 15% by weight, CIAcid Blue 112 0.1% by weight, N-octyl-N, N-dimethyl-N-benzylammonium chloride 1% by weight and the balance water, pH 6.5 An aqueous liquid composition (20 ° C.) was prepared (product of the present invention). The pH was adjusted with a 0.1 N sulfuric acid aqueous solution and a 0.1 N sodium hydroxide aqueous solution.
In addition, the same composition as that described above except that it does not contain Calcoat Marcoat 280 was prepared (comparative product).

  Each 5 ml of the product of the present invention and the comparative product were dropped with a dropper onto the hand-washing part of a toilet tank (S731B, manufactured by TOTO) that had been used at home for 10 years. Although there was a liquid flowing away in the tank, the dye was dyed in the hand-washing part. In this state, it was left at 30 ° C. for 10 days. Each composition is dried and the dye is firmly attached. Next, 3L of tap water was poured into the dried composition using a hand cup as evenly as possible over 1 minute, and when the composition was washed away, the product of the present invention was able to completely remove the dye. The product was not removed at all, and the dye was firmly attached.

  Table 1 exemplifies compositions having the effects of the present invention.

Polymer 1: Diallyldimethylammonium chloride polymer (Mercoat 100; Calgon, molecular weight 400,000)
Polymer 2: copolymer of diallyldimethylammonium chloride / maleic acid / sulfur dioxide (molar ratio 65/30/5) (molecular weight 30,000)
-Polymer 3: Copolymer of dimethylaminopropylmethacrylamide / acrylic acid (molar ratio 75/25) (molecular weight 200,000)
-Dye 1: Food Blue No. 1-Dye 2: Food Blue No. 2-Dye 3: C.I. I. Acid Blue 112
Surfactant 1: alkyl glucoside [mixture of linear alkyl group having 12 and 14 carbon atoms, glucose average condensation degree 1.2 (mixture of condensation degree 1 and 2)]
Surfactant 2: Cocoalkyldimethylbenzylammonium chloride Antibacterial agent 1: Polylysine Antibacterial agent 2: Triclosan Solvent 1: Ethylene glycol Solvent 2: Ethanol Fragrance: β-pinene (20% by mass), citronellol (20 Mass), β-ionone (15 mass%), tetrahydrolinalool (25 mass%), limonene (20 mass%)

Claims (1)

(A) 0.1 to 20% by mass of a polymer compound containing 10 to 100 mol% of a monomer unit having a tertiary amino group and / or a quaternary ammonium group in the molecule, and (b) 0.001 of an acid dye. An aqueous liquid composition containing ˜1% by mass and water.