USPatent applicationPatented

Low residue surface treatment

Granted 13 Jul 2004 · 4 office actions

Application· this page
9629368
filed 31 Jul 2000
Publication
Not published
not published
Patent
US 6,762,157
granted 13 Jul 2004

Life of the application

13 dated events
⤢ drag to zoom20002002200420062008201020122014201620182020ProsecutionOwnershipTerm & fees
ProsecutionOwnershipTerm & feeshover for detail · click to open

Abstract

An aqueous composition for the reduction or elimination of unpleasant odors from surfaces containing such odors comprises a perfume, a surfactant/solubilizer, a solvent/drying aid, an odor absorber, and, preferably, a buffer to maintain the desired pH. The solution contains minimal or no volatile organic compounds. Due to the specific nature of the combination of the surfactant/solubilizer and the solvent/drying aid, the use of fragrances previously too hydrophobic for use in an aqueous solution is possible, providing a large variety of efficient odor counteractants not previously available. The composition may optionally comprise additional components, such as preservatives, antimicrobials, anti-static compositions, anti-wrinkling agents, insect control agents, moth repellents, UV protectants, water-proofing agents, and textile treatment agents. The aqueous solution may be applied to a variety of surfaces, in sufficient quantity to wet the surface, preferably by spraying.

Description

10 parts
›RELATED APPLICATION(S)

Not applicable.

›FEDERALLY SPONSORED RESEARCH OR DEVELOPMENT

Not applicable.

›TECHNICAL FIELD

The present invention relates to aqueous compositions for reduction of objectionable odors from surfaces, comprising water, an odor absorber or odor in counteractant, perfume, solvent, solubilizer, and drying aid. The composition is designed to reduce the presence of objectionable odors, such as food odors, tobacco odors, perspiration, etc., on surfaces such as clothing or fabric such as on furniture. The compositions of the present invention are fast drying, and leave little or no residue on the surface after drying. While specifically designed for use with soft surfaces, such as fabrics, the compositions of the present invention may also be used on hard surfaces, such as garbage and refuse containers and recycling bins, or on such surfaces as appliances, counters, floors, cabinets, walls, and plumbing fixtures in kitchens and bath rooms.

›BACKGROUND OF THE INVENTION

The present invention relates to an aqueous composition suitable for use as a freshening composition. Such a composition may be sprayed onto fabrics, particularly clothing, to restore the freshness thereof by elimination or reduction of malodors, between washings or dry cleanings. The composition may also be sprayed upon fabric covered furniture, or other surfaces, to eliminate malodors, such as pet odors, or tobacco odor, without deposition of a residue upon the surface.

A wide variety of deodorizing compositions are known, most commonly containing a perfume to mask or hide the malodor. Odor masking is the intentional concealment of one odor by over-powering it with another, preferably more acceptable odor, such as a fragrance. The masking perfumes used vary greatly, dependent upon application, such as masking perspiration odor, bathroom odor, pet odors, tobacco, etc. The appropriate fragrance for a given composition needs to be selected in accordance with the end product usage, as well as the goal to give the impression of freshness.

Odor modification, i.e. changing the odor by chemical modification, has also been used. Such techniques include oxidative degradation, which uses oxidizing agents such as oxygen bleaches, chlorine, sodium hypochlorite, or similar materials. In addition, reductive degradation has been attempted, using reducing agents such as sodium bisulfite to reduce malodor. However, both of these techniques are unacceptable due to damage they cause to fabrics, especially colored fabrics.

Other odor control methods employ actives which react with malodors having specific functional groups, such as biguanide polymers, which complex with organically bound nitrogen and/or sulfur atoms, or fatty alcohol esters of methyl methacrylic acid, which react with thiols, amine, and aldehydes. Such reactive materials, however, are generally not water soluble.

In addition, antibacterial and antifungal agents which regulate the odor producing microorganisms found on surfaces, have been employed, but are ineffective on malodors not caused by bacterial sources.

The present invention is most specifically directed at environmental odors, such as tobacco odor, cooking and food odors, and body odor. These odors are generally organic in nature, and frequently result from low molecular weight, straight-chain, branched, and unsaturated C 6 -C 11 fatty acids.

U.S. Pat. No. 5,670,475, of Trinh et al is one of a number of patents related to the concept of reducing “malodor impression” from surfaces. Other relevant Trinh et al patents include U.S. Pat. Nos. 5,578,563; 5,633,134; 5,783,544; 5,968,404; 5,939,060; and 6,077,318. U.S. Pat. No. 5,670,475 teaches aqueous deodorizing compositions comprising up to about 1% perfume, and preferably including water-soluble cyclodextrins, water-soluble metal salts, and solubilizing aids. Cyclodextrins function in a manner similar to molecular sieves, which are also employed to entrap perfumes, odors, etc., and which may also be employed for removal of malodor from surfaces. Exemplary metal salts include zinc salts such as zinc sulfate, and exemplary solubilizers include ethoxylated aliphatic alcohols. In the preferred embodiments of the patent, the perfumes used in the compositions are those having a C log P of less than 3, it being indicated that such perfumes may be solubilized in water without the use of a solubilizing alcohol, whereas those perfumes with a C log P value greater than about 3 are less useful due to greater hydrophobicity. The patentee indicates that the composition contains less than about 5% low molecular weight monohydric alcohol. Cyclodextrin molecules are known to form complexes with perfume ingredients, and have been used as perfume carriers in the past. Trinh et al teach that fabrics treated with cyclodextrin exhibit perfume release upon rewetting, resulting in an impression of freshness of the fabric when said fabric is rewetted.

However, the prior art compositions are subject to slow rates of drying, and deposition of residues on the substrates treated. It is also to be noted that the Trinh et al reference specifically suggests that the perfumes used be those having a C log P value of 3 or less, to require the use of predominant proportions of those perfumes which are most hydrophilic or water soluble. This limitation prevents the utilization of a large number of popular and effective scents useful for the purpose of reducing malodor impression.

However, it is also to be noted that the presence of volatile organic compounds, or VOCs, such as alcohols, is not desirable, even though they are very effective solubilizers for perfumes, and impart rapid dry time to a surface treatment system. Such solvents are often odor objectionable in themselves, as well as being environmentally undesirable. Accordingly, it is an object of the present invention to provide a water-based deodorizing composition for treatment of surfaces, said composition preferably not containing objectionable VOCs, while still permitting the use of hydrophobic fragrances.

›SUMMARY OF THE INVENTION

In one aspect, the invention is directed to a water-based deodorizing composition for the treatment of surfaces, the composition having a good dry time without use of volatile ingredients such as alcohols, and leaving little or no residue on the surface treated. The invention also relates to methods for using this composition for deodorizing surfaces such as fabrics and clothing.

In yet another form, the invention provides a low residue treatment for the removal of odors on surfaces, using a composition containing fragrances with a C log P value greater than about 3. The composition of the present invention further removes odors without damage to surfaces, and has an acceptable dry time without the addition of VOCs.

The compositions of this invention may be applied to any surface which would not be damaged, objectionably spotted, or otherwise compromised by the application of an aqueous spray, if that surface is subject to malodor retention. For example, one would not spray a rice paper screen with an aqueous composition of the present invention, but one may use said composition on the surface of a cloth or wooden screen, or a leather or fabric car seat. The present compositions are not intended as cleansing agents, such as may be used to clean a hard surface such as a glass table, mirror, kitchen counter, toilet, or trash receptacle, but such compositions may be sprayed upon such surfaces if they have become odorous. In such cases, the surface should first be cleaned in a conventional manner, and then the composition should be sprayed upon the cleaned surface and allowed to dry without wiping, to minimize streaking or clouding of the surface, particularly of shiny surfaces, while providing maximum deodorizing effect. As indicated, the compositions of this invention are primarily intended for use on soft surfaces, such as clothing, shoes, carpeting, upholstery, curtains, draperies, linens, etc., but are not limited to such surfaces. These compositions, by virtue of the fact that they leave little or no residue upon drying, and are non-staining, non-toxic and non-injurious to most surfaces when used as intended, may be used upon almost any surface which may be contacted with an aqueous spray, such as kitchen and bath counters, appliances, and fixtures, floors, walls, and containers such as garbage cans, storage bins, etc., which are subject to malodor retention from materials with which they come in contact, or from air borne malodors such as smoke and tobacco odors.

Preferred embodiments of the invention contain a solvent to surfactant ratio of approximately 2:1, and a fragrance to surfactant ratio of 1:3. The compositions taught also exhibit a preferred skin compatible pH range of from 5 to 6, although a pH range of from about 3 to about 7 is acceptable. More-over, the composition may be incorporated into a spray dispenser to create a consumer product which may be readily used in the home or elsewhere to reduce or eliminate objectionable odors upon a surface without leaving a stain or residue.

Thus, a primary object of the invention is to provide an aqueous composition which may be applied, preferably but not necessarily as a spray, to a surface to lessen or eliminate the presence of malodors in or on said surface. Another object is to provide a means for removal of objectionable odors from fabrics, such as clothing, without staining the fabric or leaving an objectionable residue thereupon, preferably without the use of compositions containing objectionable VOCs.

The objects of the present invention therefore include providing a fragranced is aqueous composition comprising, for example, a butyl ether solvent and drying aid, a primary alcohol ethoxylate solvent or solubilizer for the fragrance, a metal salt odor absorber, pH adjustment means, and a preservative.

These and still other objects and advantages of the present invention (e.g. methods for using such compositions) will be apparent from the description which follows, which description is merely of the preferred embodiments. Thus, the claims should be looked to in order to understand the full scope of the invention.

›DETAILED DESCRIPTION OF THE INVENTION · 1 of 3

Aqueous solutions of active ingredients are used in the present invention for the treatment of surfaces to eliminate or reduce odors. The preferred carrier is accordingly water, per se, which may be softened, distilled, deionized, or tap water, and which is relatively pure, containing no material which will leave a residue or stain upon surfaces, such as fabric, upon which the solution is sprayed and allowed to dry. The water also should preferably contain little or no low molecular weight alcohol, or other VOCs. Such materials may be present in limited amounts due to their presence in some perfumes, preservatives, and/or stabilizers, but it is preferred that the level of such VOCs be limited to less than about 1 percent, and preferably less than about 0.25 percent.

The present invention thus relates to an aqueous composition for reduction of objectionable odors from surfaces, said composition comprising water, odor absorber, fragrance, a surfactant/solubilizer, and a solvent/drying aid. More specifically, the composition comprises from about 0.01 to about 1.0 weight percent of a fragrance or perfume, said perfume being any perfume which exhibits water solubility sufficient, in the presence of a solubilizer therefor, for the purpose of the invention. Such perfumes are a matter of individual taste and preference, and may be varied to satisfy the preferences of differing markets internationally, or to complement or counter the specific malodor being attacked.

The perfumes suitable for use in the present invention are those which have odor characteristics acceptable for the purpose of reducing or eliminating the impression of unacceptable odors, primarily by masking such unacceptable odors. Whereas in the past, the fragrance materials used for such purpose were limited by their hydrophobic nature, applicant has now determined that many previously unsuitable fragrances may be used in the aqueous solutions of the present invention, but only if utilized with specific surfactant/solubilizers as set forth herein. For example, the perfumes suitable for use in the present invention include such perfumes as are commonly referred to as fresh clean, spicy, floral, citrus, ozone, and marine types. Preferred perfumes are selected from those referred to as fresh clean, and floral types. Preferably, the treatment solution of the present invention contains an effective amount of perfume to provide a freshening fragrance to surfaces upon first application, and some lingering fragrance during wear, and after drying to the touch. Effective levels of perfume are from about 0.01 percent to about 1.0 percent, preferably from about 0.01 percent to about 0.5 percent, and most preferably from about 0.015 percent to about 0.3 percent by weight.

To achieve the utilization of many more desirable fragrances in the present invention, it is necessary to provide for their solubilization in the water base of the composition. It has now been found that fragrances with a C log P value of greater than 3 may be utilized in the present invention, whereas previous attempts to utilize such fragrances have been unsuccessful. The term C log P as used herein refers to the degree of hydrophobicity of a perfume ingredient, correlated with the octanol/water partitioning coefficient thereof, P. Higher P values are more hydrophobic, and since the partitioning coefficients are normally high values, they are conventionally ally referred to in the form of their logarithm to the base 10, or log P. The log P values of many perfume ingredients are readily available from such sources as the Pomona 92 database, available from Daylight Chemical Information Systems, Inc. (Daylight CIS), Irvine, Calif. However, the log P values are most conveniently calculated by the use of the “C log P” program, also available from Daylight CIS. The “calculated log P” (C log P) is based upon the fragment approach of Hansch and Leo (A. Leo, in Comprehensive Medicinal Chemistry , Vol. 4, C. Hansch, P. G. Sammens, J. B. Taylor, and C. A. Ramsden, Eds., p.295, Pergamon Press, 1990, incorporated herein by reference). The C log P values are considered the most reliable and widely used estimates for this important property, and are used instead of experimental log P values in evaluation of hydrophobicity of fragrance ingredients.

It has now been found that such fragrances may be utilized in the presence of a specific surfactant, or a combination of surfactants of the same or differing classes of surfactants, which act as a solubilizer for fragrances having a C log P value greater than about 3, in combination with a specific class of compounds normally referred to as solvents, but which in the present application act as a wetting agent and drying aid. Accordingly, the term surfactant/solubilizer, as used hereinafter, shall be meant to refer to individual surfactants, combinations of surfactants from the same class (ionic, non-ionic, cationic, or amphoteric), and combinations of surfactants from different classes, which have the ability to solubilize perfumes having a C log P higher than about 3. Suitable surfactant/solubilizers for the present invention have been found to include such surfactants as C 9-11 linear primary alcohol ethoxylates. Other suitable surfactant/solubilizers for use in the present invention include such non-ionics as ethoxylated fatty alcohols, C 9-11 linear primary alcohols, polyoxyethylene oleyl ethers, and alkoxylated biodegradable hydrotropes; such anionics as ether sulfates and linear ethylene oxide; selected cationics such as quatemary ammonium halides; and selected amphoterics including betaines such as capryloamidopropyl betaine. Thus, the surfactant/solubilizer may preferably be selected from the group consisting of linear primary alcohols, ethoxylated fatty alcohols, linear primary alcohol ethoxylates, polyoxyethylene ethers, alkoxylated biodegradable hydrotropes, linear ethylene oxide, quatemary ammonium halides, betaines, amine oxides, and mixtures thereof. Such surfactant/solubilizers may be used individually or in combination, based upon the solubility parameters of the fragrance to be employed, and may be present in concentrations of from about 0.1 to about 10.0 weight percent and preferably from about 0.5 to 5 weight percent. In the most preferred embodiments of the invention, a C 9-11 linear primary alcohol ethoxylate surfactant was employed in a concentration of from 1 to 2 percent by weight.

›DETAILED DESCRIPTION OF THE INVENTION · 2 of 3

However, it has been found that when a sufficient quantity of the surfactant/solubilizer is employed to ensure dissolution of the fragrance oil, the surfactant/solubilizer frequently leaves a residue, or stain, upon drying. Accordingly, it is desirable to employ an additional solvent material to aid in solubilizing the fragrance, and to help to wet the fabric to which the solution is applied. Since this solvent also acts to enhance drying of the solution, it shall be referred to hereinafter as a solvent/drying aid. Suitable compositions for this purpose include certain water soluble non-VOC solvents, such as butyl carbitol, a diethylene glycol butyl ether. It has been found that both carbitol and butyl carbitol are suitable, and that while butyl carbitol may be preferable for environmental reasons, mixtures of both may be particularly useful. Such solvent drying aids include such compounds as glycol ethers such as ethylene glycol butyl ether, tri(propylene glycol)methyl ether, 1-methoxy-2-propanol, diethylene glycol monoethyl ether, and glycol ether acetates such as propylene glycol methyl ether acetate, and may be present in concentrations of from about 0.05 to about 20 weight percent. In a preferred embodiment of the invention, butyl carbitol was present in a concentration of 4.5 weight percent. Preferred ranges for the solvent/drying aids may range from 1 to about 10 weight percent, more preferably from about 3 to 6 weight percent of the composition, and most preferably from about 4 to 5 weight percent of the composition.

In addition, from about 0.05 to about 5.0 weight percent of an odor absorbing metal salt should be present, selected from the group consisting of water soluble salts of metals such as zinc, copper, silver, zirconium, nickel, chromium and other transition metals. Such salts may include those acetates, chlorides, sulfates, nitrates, gluconates, maleates, lactates, salicylates, and other salts as are water soluble and have odor absorption characteristics. Thus, suitable odor control agents may comprise from 0.05 to about 5.0 weight percent, and preferably from about 0.075 to about 0.2 weight percent (based upon the total weight of the composition) of a water soluble salt selected from the group consisting of the acetates, chlorides, sulfates, nitrates, gluconates, maleates, lactates, and salicylates of zinc, copper, silver, titanium, zirconium, nickel, chromium, and other transition metals.

In addition to the above, it has been found highly beneficial to include in the composition a pH buffering agent, preferably sodium citrate, which may be used in combination with a buffering acid to combat pH drift which occurs upon heating of an aqueous solution of the above noted components. The purpose of a buffering agent is to permit a solution to resist changes in concentration of H + ions in solution, due to either internal or external influences, such as heating, which may be encountered during storage and shipment of commercial product. Buffers are conventionally composed of weak acids and bases, which do not completely ionize in solution. A combination of sodium citrate and citric acid is the preferred buffering agent for the present invention, due to the presence of three carbonyl groups, resulting in three different pK a values. Metal salt odor control agents, such as zinc salts, are difficult to stabilize, since zinc ions, for example, tend to form insoluble salts in solution, which may result in a shift in pH, which may result in discoloration or corrosion. Accordingly, it was desired that a buffer system with a pKa value within 1 unit of the desired pH range of 4.5 to 5.5 be selected. It was found that the combination of sodium citrate with citric acid controlled the pH, by serving as a ligand and complexing with the metal from the odor controlling metal salt, to form a chelate which tied up the chemical reactivity, but not the odor complexing capabilities of the metal ions. The target pH for the present invention is in the range of from about 4.5 to about 5.5, while the effective pK a values for citric acid in such a solution are from about 4.7 to about 5.4, creating an effective system to control the formula pH in the target range. While sodium citrate is the preferred citrate, other citrates, such as potassium citrate, are also suitable. Other acids in the appropriate pKa range may also be used in place of citric acid, such as succinic and acetic acids. Appropriate amounts of buffering agent, comprising a citrate salt in combination with a buffering acid, should be added to achieve the desired pH. Buffering acid may be added in addition, to arrive at the appropriate target pH range. It is also to be noted that a buffering acid may not be required if the surfactant itself is acidic and can thus serve as an ion donor.

Still further, optional components may be included, such as from 0 to about 1.0 weight percent of a preservative or stabilizer; from 0 to about 10.0 weight percent of a moth or insect repellant; from 0 to about 10 weight percent anti-static compound; from 0 to about 5 weight percent of an antimicrobial compound; and from 0 to about 0.5 weight percent of a coloring agent. Other suitable optional components may be added, as will be apparent to those skilled in the art, without detracting from the efficacy of the presently set forth compositions, and such shall be considered within the scope of the present invention.

As indicated, a preservative may also be present, although not required for the purpose of the present invention. Suitable preservatives are well known in the art, and include such compositions as Kathon® CG, a 5-Chloro-2-methyl-4-isothiazolin-3one compound available from Rohm & Haas. The concentration of preservative should be sufficient to perform the function for which it is added, and may be, for example, 0.05 weight percent of the composition. The preservative may be any organic preservative material which will not cause damage to the surfaces to which the solutions are to be applied, such as discoloration, coloration, or bleaching. Preferred water soluble preservatives include organic sulfur compounds, halogenated compounds, cyclic organic nitrogen compounds, low molecular weight aldehydes, quaternary compounds, dihydroacetic acid, phenyl and phenoxy compounds, and mixtures thereof.

›DETAILED DESCRIPTION OF THE INVENTION · 3 of 3

In addition, antimicrobial or antibacterial compositions may also be present, although not required in the present invention. Suitable compounds for this purpose include such compounds as Myristalkonium chloride and Quatemium 14. Other well known water soluble antimicrobial agents may be used, such as Benzylkonium chloride, zinc gluconate, anti-microbial anionic surfactants, and quatemary amphoteric surfactants.

Still further, other compositions may be present for specific purposes, such as anti-static, and anti-wrinkling additives. Suitable compositions for these purposes include monoalkyl cationic quatemary ammonium compounds, polyethylene glycols, polymeric quaternary ammonium salts, quaternized polyethyleneimines, etc, Other textile treatment agents like water-proofing, flame retardants, UV protectants or stain repellents may also be appropriate.

Insect control or moth repelling agents may also be optionally included, such as pheromones, citronellol, citranellal, citral, linalool, etc. Many such compositions are known in the art, and the specific agents employed are a matter of choice, dependent upon the specific need of the consumer.

The aqueous solutions of the present invention may be utilized in a variety of ways. The most commonly employed method for application of malodor counteractants is to spray the composition on the surface of the fabric, clothing, furniture, or other object which is subject to the presence of the unpleasant odor, spraying sufficient solution to slightly dampen the surface. This is most easily accomplished by means of a spray bottle, comprising a container, most favorably a light weight flexible plastic, and a spray nozzle means by which the liquid may be forced, under pressure provided by either a pump mechanism or by pressurization of the container. Such a spray application of the solution of the present invention is accordingly considered within the scope of the invention, as is the means thereof including both liquid spray, as above, and aerosol application. In addition, it is possible that the solution of the present invention may be applied by alternative means, such as by addition to a rinse cycle during laundering or dry-cleaning, or by direct application of the liquid solution to the surface by pouring, rubbing with a liquid containing absorbent material, etc. Preferably, the amount of solution applied need not saturate or cause a pooling of liquid on the article or surface, but should be sufficient to achieve the elimination or decrease of malodor without leaving a readily discernible visible deposit after drying.

›EXAMPLES

A number of test materials were mixed and evaluated for clarity and residue remaining on a fabric sample after drying. These results are shown in Tables 1A and 1B. The test samples in each instance in Table 1A contained 4 weight percent diethylene glycol monoethyl ether as a solvent/drying aid, and 0.3 weight percent of fragrance. The first group of surfactant/solubilizers were subjected to a general screening test to determine whether an acceptable residue level could be achieved. These four samples were adjusted to the appropriate pH range with citric acid alone, with no sodium citrate. The remaining examples, using the C 9-11 ethoxylate surfactant/solubilizer, all had a pH buffer, comprising both citric acid and sodium citrate, present.

In Table 1B, the results of a screening test of possible solvent/dryers is shown. In these examples, the tested solvent/dryers were evaluated in solution with 2 weight percent of C 9-11 linear primary alcohol ethoxylate surfactant/solubilizer, 0.3 percent fragrance, sufficient buffering agent to maintain the desired pH, and a zinc salt deodorizer.

In addition to optimizing the formulations containing both ethylene glycol butyl ether and C 9-11 linear primary alcohol ethoxylate, additional glycol ethers were evaluated. Results of these experiments are shown in Table 2.

After these experiments, various fragrances, including fresh clean, heavy floral, and fresh clean 2, all having a C log P greater than 3, were tested with a preferred combination of butyl carbitol and carbitol with C 9-11 linear primary alcohol ethoxylate, and found to be soluble. These dissolved fragrances were then sprayed on fabrics, and found to leave little or no residue, to dry relatively quickly, and to leave a pleasant impression.

›INDUSTRIAL APPLICABILITY

The present invention provides a readily produced combination of materials, using chemicals and compositions which are commonly available for the freshening of various fabrics and other surfaces and removal of malodors. Further, the surface treatment compositions provided present a positive improvement over those compositions presently employed for the same purposes. The methods of preparation and application of the solutions of the present invention are readily achievable by one is skilled in the art.

While the present invention has been described with respect to what are at present considered to be the preferred embodiments, it is to be understood that the invention is not to be limited to the disclosed embodiments. To the contrary, the invention is intended to cover various modifications and equivalent arrangements within the spirit and scope of the appended claims. The scope of the following claims is to be accorded the broadest interpretation so as to encompass all such modifications and equivalent formulations and functions.

›Tables in the description — 3
TABLE 1A
Surfactant/solubilizerClass%pHClarityResidue
capryloamidopropylampho-2.005.67milkynot sprayed
betaineteric
Cetyl betaineampho-2.004.57clearnone
teric
Sodium laurylanionic2.007.25hazynone
sarcosinate, 30%
Ammonium laurethanionic2.004.73milkynone
sulfate EA2
Sodium lauryl sulfateanionic2.004.12milkynone
Cocamidopropylnonionic2.005.26clearnone
amine oxide
C9-11 linear primarynonionic0.305.27cloudynot sprayed
alcohol ethoxylate
C9-11 linear primarynonionic0.605.26cloudynot sprayed
alcohol ethoxylate
C9-11 linear primarynonionic0.905.21hazynot sprayed
alcohol ethoxylate
C9-11 linear primarynonionic1.205.21clearnot sprayed
alcohol ethoxylate
C9-11 linear primarynonionic1.505.23clearnot sprayed
alcohol ethoxylate
C9-11 linear primarynonionic1.805.21clearnot sprayed
alcohol ethoxylate
C9-11 linear primarynonionic5.005.46clearvisible
alcohol ethoxylate
C9-11 linear primarynonionic7.005.47clearvisible
alcohol ethoxylate
TABLE 1B
Solvent/dryerType%pHClarityResidue
tri(propylene glycol)glycol4.004.85clearnone
methyl etherether
ethylene glycol butyl etherglycol4.005.26clearvisible
ether
1-methoxy-2-propanolglycol4.004.97clearvisible
ether
Diethylene glycolglycol0.005.28clearvisible
butyl etherether
Diethylene glycolglycol1.005.03clearvisible
butyl etherether
Diethylene glycolglycol2.005.17clearslightly
butyl etherethervisible
Diethylene glycolglycol0.505.32clearvisible
butyl etherether
Diethylene glycolglycol1.505.33clearvisible
butyl etherether
Diethylene glycolglycol10.005.48clearnone
butyl etherether
Diethylene glycolglycol1.005.48clearvisible
monoethyl etherether
Diethylene glycolglycol2.005.12clearvisible
monoethyl etherether
Diethylene glycolglycol0.505.31clearvisible
monoethyl etherether
Diethylene glycolglycol1.505.21clearvisible
monoethyl etherether
TABLE 2
Raw material190-1190-2190-3190-4190-5190-6191-1191-2191-3191-4
Diethylene glycol butyl ether2.5003.0002.5002.5003.0002.5003.0000.0000.0002.750
Tri(propylene glycol) methyl ether0.0000.0000.0000.0000.0000.0000.0002.5002.5000.000
C9-11 linear primary alcohol1.0001.0001.1001.2001.2001.5001.5001.2001.5001.500
ethoxylate
Zinc sulfate heptahydrate0.1100.1100.1100.1100.1100.1100.1100.1100.1100.110
Sodium citrate0.1500.1500.1500.1500.1500.1500.1500.1500.1500.150
Citric acid (50%)0.0260.0260.0260.0260.0260.0260.0260.0260.0260.026
Myristalkonium chloride and0.4300.4300.4300.4300.4300.4300.4300.4300.4300.430
Quaternarium 14 antimicrobials
Fresh floral fragrance0.3000.3000.3000.3000.3000.3000.3000.3000.3000.300
Distilled waterqsqsqsqsqsqsqsqsqsqs
TOTAL100.00100.00100.00100.00100.00100.00100.00100.00100.00100.00
pH5.145.175.115.225.185.045.175.145.215.17
Appearance of solutionclearclearclearclearclearclearclearclearclearclear
Appearance of solution after
24 hours at room temperatureclearclearclearclearclearclearclearclearclearclear
24 hours at 50° F.hazyhazyclearhazyclearclear
24 hours at 100° F.clearclearclearclearclearclearclearclearclearclear

Claims as granted

17 claims

Log in to read the claims of this application.

Log in to unlock

Classifications

12 codes
IPC · International Patent Classification
Section A — Human necessities
  • A61L9/14
  • A61L9/01
Section C — Chemistry; metallurgy
  • C11D3/20
  • C11D3/02
  • C11D3/43
  • C11D3/00
USPC · US Patent Classification
510/101510/518510/524510/535510/506510/289

Claim changes

Soon
Coming soonHow the claims changed between publication and grant

See which claims were amended, added or cancelled during examination, with every added and removed word marked.

AmendedAddedCancelledUnchanged

The published claims of this application are not paired with the granted ones in what we hold.

File wrapper

⤢ drag to zoomJul 2000Jan 2001Jul 2001Jan 2002Jul 2002Jan 2003Jul 2003Jan 2004Jul 2004USPTOApplicantNon-final rejectionResponse after non-finalRequest for continued examinationResponse after non-finalRequest for continued examination
USPTOApplicanthover for detail · click to open
Pendency
4.0 y
1,443 days filing → grant
Office actions
4
non-final + final
Responses
2
2 RCE
Examiner
Brian P. Mruk
art unit 1751 · TC 1700
Citations: 11 back · 20 forward

See the full prosecution history — every USPTO and applicant action on this file, in order.

Log in to unlock

Documents

Log in to open the documents of this file: the application as filed, every office action and response, the notice of allowance.

Log in to unlock

Chain of title

⤢ drag to zoom20002002200420062008201020122014201620182020Owner 1
Titlehover for detail · click to open

See the full assignment history — every owner this patent has passed through, with recordation dates and reel/frame numbers.

Log in to unlock