Neutral liquid detergent composition.
2 claims: 1 independent, 1 dependent
- 1A neutral liquid detergent composition comprising:(a) 2-60% by weight of an alkyl glycoside represented by the following formula (I): R₁(OR₂) x G y (I) wherein R₁ is a linear or branched alkyl, alkenyl, or alkylphenyl group having 8-18 carbon atoms, R₂ is an alkylene group having 2-4 carbon atoms, G is a reducing saccharide residue having 5-6 carbon atoms, x is a number of which the mean value is 0-5, and y is a number of which the mean value is 1.0-1.42;(b) 0.1-10% by weight of a nonionic surfactant having an HLB of less than 5;(c) 0.1-10% by weight of a nonionic surfactant having an HLB of not less than 5;and (d) 0.001-8% by weight of one or more water-soluble organic or inorganic salts selected from the group consisting of sulfates, chlorides, borates, phosphates, p-toluensulfonates, m-xylenesulfonates, benzoates, malates, succinates, tartarates, citrates, lactates, and edates of sodium and potassium and mixtures thereof;the ratio by weight of component [(b)+(c)]/(a) being in a range of 1/10-1/1 and the ratio by weight of component (b)/(c) being in a range of 1/10-1/1.
- 2A neutral liquid detergent composition according to Claim 1, further comprising one or more surfactants selected from 1-20% by weight of anionic surfactants, 1-20% by weight of amphoteric surfactants, and 1-10% by weight of nonionic surfactants other than components (a)-(c).
Independent claims2
53 paragraphs in 4 sections, as filed
BACKGROUND OF THE INVENTION
Field of the Invention
:
0001The present invention relates to a detergent composition, and, more particularly, to a neutral liquid detergent composition exhibiting remarkably reduced irritation and damage to the hair or the skin, possessing high foaming ability, and imparting a favorable feeling upon use. The detergent composition has also good rinsability of foam and excellent drainability from tableware and the like after washing.
Description of the Background Art:
0002Because of increased awareness for safety towards the human body in recent years, a number of trials have been undertaken in order to moderate the action of detergent compositions which frequently contact the skin. Such detergent compositions include laundry detergents, dishwashing detergents, household detergents, hair shampoos, and body shampoos. One of the approaches is adjusting the pH of detergent compositions to a weakly acidic range, e.g. pH 5-6, close to the intrinsic pH of human skins so as to be mild to the skin. Another approach is to incorporate low irritant components as major detergent base components. For example, amino acid surfactants, alkyl phosphate surfactants, or the like are being used as a low irritant detergent (Japanese Patent Publication Nos. 40125/1975, 426023/1976, 9033/1980, and 27319/1983).
0003Even though these surfactants are low irritant, they do not necessarily exhibit sufficient detergency and foaming ability is also their drawback. On the other hand, sodium alkylbenzenesulfonates have conventionally been popular detergent base components for dishwashing detergents because of their strong detergency. The compounds, however, give a strong defattying action to the skin and thus can be a cause of roughened hands.
0004Because of these reasons, sodium alkylethoxysulfates which are less irritant to the skin have gained a wider popularity as the base components for dishwashing detergents in recent years. Their detergent performances are even promoted by incorporating co-surfactants such as tertiary alkyl amine oxides, higher fatty acid diethanolamides, and the like. Their mildness to the skin is also improved by such a combination as compared with conventional detergent compositions.
0005The mildness to the skin of the detergents has improved to some degree as described above, nevertheless the achievement at present is still unsatisfactory.
0006Alkyl glycosides, being saccharide-derived surface active agents, are less irritant compounds. Although they are nonionic surfactants, it is well known that they not only produce stable foam themselves but also can act as a foam stabilizer for anionic surfactants. Thus, alkyl glycosides are gaining much attention in recent years. EP-A-0 105 556 and EP-A-0 075 995 disclose detergent compositions containing alkylpolysaccharides and nonionic surfactants.
0007Japanese Patent Laid-open No. 104625/1983, for example, discloses a foaming surfactant composition comprising an alkyl glycoside and an anionic surface active agent, and Japanese Patent Laid-open No. 74999/1987 discloses a liquid dishwashing detergent composition comprising an alkyl glycoside, an anionic surface active agent, and a fatty acid alkanolamide. They claim that the compositions are low irritant and have an excellent detergency. Even though these detergent compositions exhibit performances better than conventional detergent compositions containing polyoxyethylenealkylethers as a base component, such performances are still to be improved. They have problems such as an inferior feeling upon use, poor rinsability of the foam, and insufficient drainability.
0008In view of this situation, the present inventors have conducted extensive studies to make the maximum use of the characteristics of alkyl glycosides, and found that a detergent composition which exhibits an excellent feeling upon use, good rinsability of the foam, and superior drainability by incorporating alkyl glycosides together with a specific amount of certain type of nonionic surfactant having a specific HLB other than alkyl glycosides and a specific amount of certain type of water-soluble salt. Such findings have led to the completion of this invention.
SUMMARY OF THE INVENTION
0009Accordingly, an object of the present invention is to provide a neutral liquid detergent composition comprising: <ul id="ul0001" list-style="none"><li>(a) 2-60% by weight of an alkyl glycoside represented by the following formula (I): R₁(OR₂)<sub>x</sub>G<sub>y</sub> (I) wherein R₁ is a linear or branched alkyl, alkenyl, or alkylphenyl group having 8-18 carbon atoms, R₂ is an alkylene group having 2-4 carbon atoms, G is a reducing saccharide residue having 5-6 carbon atoms, x is a number of which the mean value is 0-5, and y is a number of which the mean value is 1.0-1.42;</li><li>(b) 0.1-10% by weight of a nonionic surfactant having an HLB of less than 5;</li><li>(c) 0.1-10% by weight of a nonionic surfactant having an HLB of not less than 5; and</li><li>(d) 0.001-8% by weight of one or more water-soluble organic or inorganic salts selected from the group consisting of sulfates, chlorides, borates, phosphates, p-toluenesulfonates, m-xylenesulfonates, benzoates, malates, succinates, tartarates, citrates, lactates, and edates of sodium and potassium; the ratio by weight of components <maths id="math0001" num=""><math display="inline"><mrow><mtext>[(b)+(c)]/(a)</mtext></mrow></math><img file="EP0408965B1_D0001.tif" /></maths> being in a range of 1/10-1/1 and the ratio by weight of components (b)/(c) being in a range of 1/10-1/1.</li></ul>
0010Other objects, features and advantages of the invention will hereinafter become more readily apparent from the following description.
DETAILED DESCRIPTION OF THE INVENTION AND PREFERRED EMBODIMENTS
0011Alkyl glycoside, component (a) of the present invention, is used as a major surfactant in the composition of the present invention. The mean value of x in formula (I), being defined as 0-5, affects the water-solubility and crystalline property of the alkyl glycosides. Higher the value x, are the alkyl glycosides more soluble in water and less crystalline. A desirable value of x is in the range of 0-2.
0012When the value y in formula (I) is larger than 1, i.e., when alkyl glycosides contain those having di- or higher saccharides as the hydrophilic groups, the saccharide chain bonds may be 1-2, 1-3, 1-4, 1-6, α-pyranoside, β-pyranoside, or franoside, or a mixture thereof. Among the preferable value of y which is 1.0-1.42, a most preferable range is about 1.10-1.40. The value y is determined by the proton NMR method.
0013R₁ in formula (I) is a C₈₋₁₈ linear or branched alkyl, alkenyl, or alkylphenyl group. From the aspect of water-solubility and foaming ability, a preferable carbon number is C₁₀₋₁₄. R₂ in formula (I) is a C₂₋₄ alkylene group. From the aspect of water-solubility and the like, a preferable carbon number is C₂₋₃. The structure of G in formula (I) depends upon whether it represents a monosaccharide or a di- or higher saccharide. Monosaccharides include glucose, galactose, xylose, mannose, lyxose and arabinose, as well as their mixtures. Examples of di- or higher saccharides are maltose, xylobiose, isomaltose, cellobiose, gentiobiose, lactose, sucrose, nigerose, turanose, raffinose, gentianose and melezitose, as well as their mixtures. Among these, from the aspect of availability and cost, preferable monosaccharides are glucose and fructose, and preferable di- or higher saccharides are maltose and sucrose.
0014Component (a) is incorporated in the composition of the present invention in an amount of 2-60%, preferably 10-40% by weight.
0015Component (b) of the present invention is nonionic surfactants having an HLB value of less than 5. The HLB value is defined as the value calculated from the equation, J. T. Davies and E. K. Rideal: <i>Interfacial Phenomena</i>, pp 371-383 (1963), Academic Press, New York.<maths id="math0002" num=""><math display="block"><mrow><mtext>HLB = 7 + Σ (number of hydrophilic groups)</mtext><mspace linebreak="newline" /><mtext> - Σ (number of hydrophobic groups)</mtext></mrow></math><img file="EP0408965B1_D0002.tif" /></maths> The number of each atomic group used for the HLB calculation is as follows. <tables id="tabl0001" num="0001"><img file="EP0408965B1_D0003.tif" /></tables>
0016Examples of component (b) are polyoxyethylene alkyl ether, polyoxyethylene alkylphenyl ether, polyoxyethylene sorbitan fatty acid ester, polyoxyethylene sorbit fatty acid ester, polyoxyethylene glycol fatty acid ester, polyoxyethylene polyoxypropylene alkyl ether, polyoxyethylene castor oil, polyoxyethylene hydrogenated castor oil, polyoxyethylene alkylamine and glycerol fatty acid ester. Component (b) is incorporated in the composition of the present invention in an amount of 0.1-10%, preferably 0.5-8% by weight.
0017Component (c) of the present invention is nonionic surfactants having an HLB value of not less than 5. Enumerated as examples of component (c) are polyoxyethylene alkyl ether, polyoxyethylene alkylphenyl ether, polyoxyethylene sorbitan fatty acid ester, polyoxyethylene sorbit fatty acid ester, polyethylene glycol fatty acid ester, polyoxyethylene polyoxypropylene alkyl ether, polyoxyethylene castor oil, polyoxyethylene hydrogenated castor oil, polyoxyethylene alkylamine and polyoxyethylene fatty acid amide, having the total adduct mols of ethylene oxide of not less than 10.
0018Component (c) is incorporated in the composition of the present invention in an amount of 0.1-10%, preferably 0.3-8% by weight.
0019The ratio of component <maths id="math0003" num=""><math display="inline"><mrow><mtext>[(b)+(c)]/(a)</mtext></mrow></math><img file="EP0408965B1_D0004.tif" /></maths> is in the range of 1/10-1/1, preferably 1/8-1/1.5 by weight. The ratio of component (b)/(c) is in the range of 1/10-1/1, preferably 1/8-1/1.5 by weight.
0020The difference in HLB between component (b) and component (c) is preferably greater than 3.
0021Component (d) used in the present invention is water-soluble organic or inorganic salt given in the aforementioned explanation. Among them, sulfates, chlorides, borates, p-toluensulfonates, benzoates, citrates, and edates of sodium and potassium are particularly preferable.
0022The composition of the present invention contains 0.001-8% by weight of component (d). A preferable amount of component (d) is 0.01-5%, and particularly 0.1-4% by weight. The amount exceeding 8% by weight not only impairs the intended effects, but also adversely affects the stability of the composition.
0023Besides the above essential components, the composition of the present invention may comprise one or more of surfactants selected from the groups consisting of anionic surfactants (1-20% by weight), amphoteric surfactants (1-20% by weight), and nonionic surfactants (1-10% by weight) other than the above components (a)-(c). These surfactants are optionally incorporated into the composition of the present invention in order to promote its detergency and foaming ability. conventionally known anionic or amphoteric surfactants can be used. Such surfactants may include, for example, α-olefin sulfonates [C₈₋₂₀; Na, K, Mg, triethanolamine (TEA), NH₄ salts], polyoxyethylene alkylsulfates (EO=2-8; alkyl group: C₈₋₁₈, linear or branched; Na, K, Mg, TEA, NH₄ salts), salts of α-sulfo-fatty acid ester represented by the formula, <chemistry id="chem0001" num="0001"><img file="EP0408965B1_D0005.tif" /></chemistry> (wherein R₅: C₈₋₁₈, R₆: C₁₋₄, M: alkali metals, M-acylglutamates (acyl group: C₈₋₁₈; Na, K, TEA salts), monoalkyl phosphates (alkyl group: C₈₋₁₈; Na, K, TEA, arginine salts), linear alkylbenzenesulfonates (alkyl group: C₁₀₋₁₈; Na, K, Mg salts), alkyl betaine, alkyl sulfobetaine and alkyl hydroxysulfobetaine. Given as examples of the nonionic surfactants other than component (a)-(c) are mono- or di-alkanol (C₂₋₃) amides of C₃₋₂₂ fatty acid, and tert-alkylamine oxides (alkyl group: C₈₋₁₈, linear or branched).
0024The pH range of a neat liquid of the detergent composition of the present invention is preferably 6-8, particularly 6.5-7.5 is most preferable.
0025In addition to the above components, other optional ingredients can be formulated into the composition of the present invention to the extent that its stability, detergency, and foaming ability are not adversely affected. Such optional components include lower aliphatic alcohols, e.g. ethanol; solubilizers, e.g. urea; viscosity adjusting agents, e.g. clay minerals, water-soluble polymers; water-insoluble abrasives, e.g. calcite, silica, calcium phosphate, zeolite, polyethylene, nylon, polystyrene; moisturizing agents, e.g. glycerol, sorbitol; feeling improvers, e.g. cationized cellulose; enzymes; perfumes; pigments; antiseptics; and antifungal agents.
0026The detergent composition of the present invention thus prepared has excellent foaming ability, is mild to the skin and the hair, and imparts a favorable feeling to the hands during and after use. The foam is easily rinsed off and after washing water is easily drained from the tableware and the like. Thus, it is a neutral detergent composition having a high practical value.
0027Other features of the invention will become apparent in the course of the following description of the exemplary embodiments which are given for illustration of the invention and are not intended to be limiting thereof.
EXAMPLES
Example 1
0028The detergent compositions having the formulations shown in Table 1 were prepared. Their foaming ability, rinsability, feeling to the hands during and after use, and drainability were evaluated. The results are shown in Table 1.
0029The feeling to the hands during and after use was tested using composition A (Composition 11 in Table 1) as a standard. Evaluation was made by comparing the feelings given to the hands when composition A and composition B (Compositions 1-10 in Table 1) were used.
〈Test Methods and Evaluation Standards〉
(1) Foaming ability
0030Foaming ability was measured on samples prepared by adding a commercially available butter in an amount of 0.1%, as a dirt component, to 0.5% detergent composition solutions. Forty milliliters of the solution of the detergent composition to which butter was added was charged into a glass cylinder with a diameter of 5 cm and subjected to a rotational stirring for 10 minutes. The height of the foam produced was measured after the termination of the stirring.
(2) Rinsability
0031Three liters of a sample solution with 0.25% detergent concentration was charged into a container (diameter: 30 cm, height: 12 cm) and rotationally stirred for 10 minutes, after which the liquid was discharged through an opening at the bottom of the container, leaving the foam in the container. Three liters of tap water was then charged to the container, and the ten-minutes stirring and discharge of liquid were repeated. This procedure was repeated until no foam was observed in the container. The number of times of tap water charge and discharge required for the foam to diminish was taken as the standard of rinsability.
(3) Feeling to the hands during and after use
0032Two 10% detergent composition solutions, A and B, at 40°C were charged into 2-liter beakers. Feeling of solutions A and B to the hands was sensuously evaluated according to the following standard.
(i) Feeling of the solution
0033Hands were dipped into solutions A and B, i.e., one hand to solution A and the other to solution B. After 1 minute, the feeling to the hands was compared according to the following standard. <tables id="tabl0002" num="0002"><table frame="all"><tgroup cols="2" colsep="1" rowsep="0"><colspec colnum="1" colname="col1" colwidth="78.75mm" /><colspec colnum="2" colname="col2" colwidth="78.75mm" /><tbody valign="top"><row><entry namest="col1" nameend="col1" align="left">B is less slimy than A</entry><entry namest="col2" nameend="col2" align="right">+2</entry></row><row><entry namest="col1" nameend="col1" align="left">B is slightly less slimy than A</entry><entry namest="col2" nameend="col2" align="right">+1</entry></row><row><entry namest="col1" nameend="col1" align="left">Hard to tell which is more slimy</entry><entry namest="col2" nameend="col2" align="right">0</entry></row><row><entry namest="col1" nameend="col1" align="left">B is slightly more slimy than A</entry><entry namest="col2" nameend="col2" align="right">-1</entry></row><row rowsep="1"><entry namest="col1" nameend="col1" align="left">B is more slimy than A</entry><entry namest="col2" nameend="col2" align="right">-2</entry></row></tbody></tgroup></table></tables>
(ii) Feeling after use
0034After the above test, the hands were thoroughly washed with water and wiped out with a dry towel. Then feeling of the hands were compared according to the following standard. <tables id="tabl0003" num="0003"><table frame="all"><tgroup cols="2" colsep="1" rowsep="0"><colspec colnum="1" colname="col1" colwidth="78.75mm" /><colspec colnum="2" colname="col2" colwidth="78.75mm" /><tbody valign="top"><row><entry namest="col1" nameend="col1" align="left">B is less sticky than A</entry><entry namest="col2" nameend="col2" align="right">+2</entry></row><row><entry namest="col1" nameend="col1" align="left">B is slightly less sticky than A</entry><entry namest="col2" nameend="col2" align="right">+1</entry></row><row><entry namest="col1" nameend="col1" align="left">Hard to tell which is more sticky</entry><entry namest="col2" nameend="col2" align="right">0</entry></row><row><entry namest="col1" nameend="col1" align="left">B is slightly more sticky than A</entry><entry namest="col2" nameend="col2" align="right">-1</entry></row><row rowsep="1"><entry namest="col1" nameend="col1" align="left">B is more sticky than A</entry><entry namest="col2" nameend="col2" align="right">-2</entry></row></tbody></tgroup></table></tables>
0035The above tests were carried out by 10 panelists. The total scores gained by solution B was taken as the feeling of the solution B.
(4) Drainability
0036Three liters of a 0.15 % detergent composition solution (in 3.5° DH at 25°C) was charged into a container (diameter: 30 cm, depth: 12 cm). A piece of porcelain dish having a 25 cm diameter was dipped into the solution for 3 minutes. The dish was taken out from the solution and dried at 25°C. This procedure was repeated 4 times. Then the dish was again dipped into the solution, following which it was taken out from the solution and rinsed for 30 seconds in a water stream and dried. The number of water spots remaining on the surface of the dish was counted to evaluate the drainability according to the following standard.
Evaluation Standard:
0037<ul id="ul0002" list-style="none"><li>A: No water spots are present</li><li>B: Less than 20 water spots are present</li><li>C: 20 or more of water spots are present</li></ul><tables id="tabl0004" num="0004"><img file="EP0408965B1_D0006.tif" /></tables><tables id="tabl0005" num="0005"><img file="EP0408965B1_D0007.tif" /></tables>
Example 2
0038<tables id="tabl0006" num="0006"><table frame="all"><tgroup cols="2" colsep="1" rowsep="0"><colspec colnum="1" colname="col1" colwidth="78.75mm" /><colspec colnum="2" colname="col2" colwidth="78.75mm" /><thead valign="top"><row><entry namest="col1" nameend="col2" align="center">Light duty liquid detergent composition for laundry</entry></row><row><entry namest="col1" nameend="col1" /><entry namest="col2" nameend="col2" align="center">% by weight</entry></row></thead><tbody valign="top"><row><entry namest="col1" nameend="col1" align="left">Alkyl glycoside 1)</entry><entry namest="col2" nameend="col2" align="right">20</entry></row><row><entry namest="col1" nameend="col1" align="left">Sodium polyoxyethylene(<o ostyle="single">p</o>=2)alkyl(C₁₂₋₁₃)ether sulfate</entry><entry namest="col2" nameend="col2" align="right">10</entry></row><row><entry namest="col1" nameend="col1" align="left">Softhanol 33 2)</entry><entry namest="col2" nameend="col2" align="right">2</entry></row><row><entry namest="col1" nameend="col1" align="left">Polyoxyethylene(<o ostyle="single">p</o>=30)lauryl ether (HLB=11.7)</entry><entry namest="col2" nameend="col2" align="right">3</entry></row><row><entry namest="col1" nameend="col1" align="left">Sodium malate</entry><entry namest="col2" nameend="col2" align="right">3</entry></row><row><entry namest="col1" nameend="col1" align="left">Ethanol</entry><entry namest="col2" nameend="col2" align="right">4</entry></row><row><entry namest="col1" nameend="col1" align="left">Perfume, enzyme</entry><entry namest="col2" nameend="col2" align="right">Small amount</entry></row><row><entry namest="col1" nameend="col1" align="left">Water</entry><entry namest="col2" nameend="col2" align="right">Balance</entry></row><row><entry namest="col1" nameend="col1" /><entry namest="col2" nameend="col2" align="right">100</entry></row><row rowsep="1"><entry namest="col1" nameend="col2" align="justify">(The above mixture was adjusted to pH 8.0) </entry></row></tbody></tgroup><tgroup cols="2" colsep="0" rowsep="0"><colspec colnum="1" colname="col1" colwidth="78.75mm" /><colspec colnum="2" colname="col2" colwidth="78.75mm" /><tbody valign="top"><row><entry namest="col1" nameend="col2" align="justify">1) In formula (I), x=1, y=1.30, R₁=C₁₀₋₁₂ alkyl, R₂=C₂ alkylene, G=glucose residue</entry></row><row><entry namest="col1" nameend="col2" align="justify">2) Trademark, a nonionic surfactant produced by Nippon Shokubai Kagaku Kogyo Co., Ltd. (HLB: about 2.4)</entry></row></tbody></tgroup></table></tables>
Example 3
0039<tables id="tabl0007" num="0007"><table frame="all"><tgroup cols="2" colsep="1" rowsep="0"><colspec colnum="1" colname="col1" colwidth="78.75mm" /><colspec colnum="2" colname="col2" colwidth="78.75mm" /><thead valign="top"><row><entry namest="col1" nameend="col2" align="center">Dishwasing detergent composition</entry></row><row><entry namest="col1" nameend="col1" /><entry namest="col2" nameend="col2" align="center">% by weight</entry></row></thead><tbody valign="top"><row><entry namest="col1" nameend="col1" align="left">Alkyl glycoside 1)</entry><entry namest="col2" nameend="col2" align="right">20</entry></row><row><entry namest="col1" nameend="col1" align="left">Sodium polyoxyethylene(<o ostyle="single">p</o>=5)laurylether sulfate</entry><entry namest="col2" nameend="col2" align="right">5</entry></row><row><entry namest="col1" nameend="col1" align="left">Glycerol monomyristate (HLB=4.4)</entry><entry namest="col2" nameend="col2" align="right">2</entry></row><row><entry namest="col1" nameend="col1" align="left">Polyoxyethylene(<o ostyle="single">p</o>=60)hydrogenated castor oil</entry><entry namest="col2" nameend="col2" align="right">5</entry></row><row><entry namest="col1" nameend="col1" align="left">Lauryldimethylamine oxide</entry><entry namest="col2" nameend="col2" align="right">2</entry></row><row><entry namest="col1" nameend="col1" align="left">Sodium sulfate</entry><entry namest="col2" nameend="col2" align="right">1</entry></row><row><entry namest="col1" nameend="col1" align="left">Ethanol</entry><entry namest="col2" nameend="col2" align="right">3</entry></row><row><entry namest="col1" nameend="col1" align="left">Perfume, enzyme</entry><entry namest="col2" nameend="col2" align="right">Small amount</entry></row><row><entry namest="col1" nameend="col1" align="left">Water</entry><entry namest="col2" nameend="col2" align="right">Balance</entry></row><row><entry namest="col1" nameend="col1" /><entry namest="col2" nameend="col2" align="right">100</entry></row><row rowsep="1"><entry namest="col1" nameend="col2" align="justify">(The above mixture was adjusted to pH 7.0) </entry></row></tbody></tgroup><tgroup cols="2" colsep="0" rowsep="0"><colspec colnum="1" colname="col1" colwidth="78.75mm" /><colspec colnum="2" colname="col2" colwidth="78.75mm" /><tbody valign="top"><row><entry namest="col1" nameend="col2" align="justify">1) In formula (I), x=0, y=1.4, R₁=C₉₋₁₁ alkyl, G=glucose residue</entry></row></tbody></tgroup></table></tables>
Contents4
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| Lapsed in a contracting state [announced via postgrant information from national office to epo]LapsedPG25 | PG25 | EP | |
| Annual fee paid to national office [announced via postgrant information from national office to epo]GrantedPGFP | PGFP | EP | |
| No opposition filedOpposition26N | 26N | EP | |
| No opposition filed within time limitOppositionORIGINAL CODE: 0009261PLBE | PLBE | EP | |
| Information on the status of an ep patent application or granted ep patentGrantedSTATUS: NO OPPOSITION FILED WITHIN TIME LIMITSTAA | STAA | EP | |
| Definitive protectionFG2A | FG2A | ES | |
| Fr: translation filedET | ET | EP | |
| Corresponds to:REF | REF | EP | |
| Designated contracting statesAK | AK | EP | |
| (expected) grantORIGINAL CODE: 0009210GRAA | GRAA | EP | |
| First examination report despatched17Q | 17Q | EP | |
| Request for examination filed17P | 17P | EP | |
| Designated contracting statesAK | AK | EP | |
| Search report despatchedORIGINAL CODE: 0009013PUAL | PUAL | EP | |
| Designated contracting statesAK | AK | EP | |
| Public reference made under article 153(3) epc to a published international application that has entered the european phaseORIGINAL CODE: 0009012PUAI | PUAI | EP |
Numbers
- Publication
- 0408965
- Publication, DOCDB
- 0408965
- Publication, EPODOC
- EP0408965
- Application
- 90112587
- Application, DOCDB
- 90112587
- Application, EPODOC
- EP19900112587
Titles6
- German
- Neutrale, flüssige Detergentzusammensetzung.
- English
- Neutral liquid detergent composition.
- French
- Composition détergente neutre et liquide.
- German
- Neutrale, flüssige Detergentzusammensetzung
- English
- Neutral liquid detergent composition
- French
- Composition détergente neutre et liquide
Classification
- CPC, 16
- A61K8/604
- A61K8/39
- A61K8/40
- A61K8/86
- A61K2800/596
- A61Q5/02
- A61Q19/10
- C11D1/29
- C11D1/662
- C11D1/667
- C11D1/72
- C11D1/75
- C11D1/825
- C11D1/83
- C11D1/94
- C11D3/0094
- IPC, 31
- A61K8 00
- A61K8 20
- A61K8 23
- A61K8 24
- A61K8 36
- A61K8 362
- A61K8 365
- A61K8 368
- A61K8 39
- A61K8 40
- A61K8 41
- A61K8 46
- A61K8 60
- A61K8 86
- A61Q5 02
- A61Q19 10
- C11D1 29
- C11D1 66
- C11D1 68
- C11D1 72
- C11D1 75
- C11D1 825
- C11D1 83
- C11D1 86
- C11D1 94
- C11D3 04
- C11D3 16
- C11D3 386
- C11D3 40
- C11D3 48
- C11D3 50
Designated states4
- Contracting states, 4
- Germany
- Spain
- France
- United Kingdom
