|Publication number||US3910880 A|
|Publication date||Oct 7, 1975|
|Filing date||Aug 13, 1973|
|Priority date||Sep 30, 1970|
|Publication number||US 3910880 A, US 3910880A, US-A-3910880, US3910880 A, US3910880A|
|Original Assignee||Lever Brothers Ltd|
|Export Citation||BiBTeX, EndNote, RefMan|
|Patent Citations (4), Referenced by (12), Classifications (28)|
|External Links: USPTO, USPTO Assignment, Espacenet|
United States Patent Lamberti Oct. 7, 1975 SULFOSUCCINATE DERIVATIVES OF  Field of Search 260/209 R. 210 R, 234 R, CARBOHYDRATES 260/2095 R. 2l2 R, 23313 R, 224, 233.5.
209.6, 209.5  inventor: Vincent Lamberti, Upper Saddle Ri N  References Cited  Assignee: Lever Brothers Company, New UNITED S1 ATES PATENTS York N Y 3 l03 507 9/1963 Knoevenagel .1 260/209 R 3,324,l()8 6/1967 Moller et alt 260/2l0 R  Filed: Aug. 13,1973 3.7712159 11/1973 Lew .1 260/210 R 2 2 4 pp No: 387,835 3,808, 00 4/l974 Bistline et ul 260/ 3 R Related US. Application Data Primary Examiner-Johnnie R. Brown 162] Division or SET. No. 222,648. Feb 1, 1972. Pat. No. Alwmey- 8 Firm-mail Y"  ABSTRACT  Foreign Application Priority Data The use of sulfosuccinate derivatives of carbohydrates Sept. 28, 1971 Germany 2148279 h as starches. Sucrosev ell l glycog n. hemicel- Sept, 28, 1971 U i d Ki d 451 1/71 lulose, gums, as biodegradable builders in detergent compositions. The aforementioned compounds can be  US. Cl 260/210 R; 252/538; 252/546; substituted in detergent compositions for existing 252/557; 260/2095; 260/2096; 260/224; builders containing phosphorus or nitrogen without 260/234 R; 260/2335 impairing the efficiency of such detergent composi- [Sl] lnt. Cl. C07H 13/12; C088 3/08; lions- 5 Claims, No Drawings SULFOSUCCINATE DERIVATIVES OF CARBOHYDRATES This application is a division of parent application Ser. No. 222,648 filed Feb. 1, I972, which issued as US. Pat. No. 3,756,966 on Sept. 4, I973.
BACKGROUND OF THE INVENTION Field of the Invention Detergent compositions containing biodegradable builders.
SUMMARY OF THE INVENTION It is an object of the present invention to provide detergent compositions containing builder compounds which are free of, or contain substantially reduced amounts of nitrogen and phosphorus, and are as effcient as existing builders containing phosphorus and nitrogen.
It is another object of the invention to provide compositions containing builder compounds which can be synthesized from low cost raw materials at reasonable prices and are biodegradable.
Still another object of the present invention is to provide new organic compounds which may be utilized as builders in detergent compositions.
DESCRIPTION OF THE INVENTION It has now been discovered that certain sulfosuccinate derivatives of carbohydrates. particularly polysaccharides, such as sucrose, lactose, maltose, cellobiose, raffinose, starches, cellulose, glycogen, hemicelluloses, pectins, alginates and gums and carbohydrate derivatives such as alkyl glycosides can serve as effective detergent builders in detergent compositions.
The builders employed in accordance with the present invention can be described as derivatives of alkyl glycosides, di-, oligoand polysaccharides having the general formula:
OR ()R n wherein A is COOM or CHgORl R is hydrogen or a sultosuccinate moiety of the formula st m1 R' is R. an alkyl group containing 1 to 4 carbon atoms or an aor ,B-tructosc moiety having the structure OR H wherein R is as defined above; M is an alkali metal, ammonium or substituted ammonium cation; n is an'integer from about l-l0,000 and wherein the average number of sulfosuccinate moieties is at least 0.5 per monomeric unit.
The aforementioned compounds can be substituted in detergent compositions for existing builders containing phosphorus or nitrogen without impairing the efficiency of such detergent compositions.
It should be understood that the above structure (Formula I), for purposes of simplicity, is entirely pictorial and represents a simplified version of the molecule. More specifically, it is well known, for example, that many starches can contain as a major constituent thereof, amylopectin or the branched chain as opposed to the amylose or linear chain molecule which is actually indicated by the pictorial representation above. Since the amylopectin polymers are linked by hemiacetal links at the uronic position, the sulfosuccinate salt derivatives of starches described in the present invention may also contain considerable branching at the uronic positions with hemiacetallinked polyglucoside chains.
In the case of cellulose, the anhydroglucose unit depicted above (Formula I) is linked as in cellobiose and the molecule may contain from about 250-2500 cellobiose units. Accordingly, it should be understood that when the degree of substitution or 05. value (i.e., number of R groups per monomeric unit) is stated, it is the average number of R groups per anhydroglucose unit that is intended in the cases of cellulose and starch. Further, in the case where alginic acid (A=COOH) is used as a starting material to prepare derivtives of the invention, the repeating unit is even more complex and monosubstituted, some may be disubsituted, some may be trisubstituted and some may be unsubstituted. Further, the sequence of such substituted and unsubstituted units, while unknown, is most probably in a random manner.
As a resuit of the complex structures present in the polysaccharide ester salts in the present invention, the degree of subsitution or esterification is referred to by the average number of sulfosuccinate moieties attached per anhydromonosaccharide unit. A degree of substitution of 0.5, for example, indicates that, on the average, for every anhydromonosaccharide units in the molecule, there are 50 sulfosuccinate moieties in thecomplex arrangement described above,
In the cases of sulfosuccinate derivatives of alkyl glycosides with "=1 and disaccharides, the D8. value refers to the total number of hydroxy groups substituted by sulfosuccinate moieties per molecule. Thus, the D.S. value may be as high as 4 in the alkyl glycoside derivatives and as high as 8 in the disaccharide derivatives.
It has been found that effective detergent-building properties are afforded when the polysaccharide sulfosuccinate salts of the present invention have a degree of subsitution (D.S. value) of from about 0.5-3, preferably about 1-3 and more preferably, l.5-3. In the cases of the sulfosuccinate salts of the disaccharides, effective detergent-building properties are afforded when the D.S. value is from about I to 8 and preferably from about 2 to 8. In the cases of the sulfosuccinate derivatives of the alkyl glycosides, the effective detergent building properties are afforded when the D.S. value is from about l to 4 and preferably from about 2 to 4.
The alkali metal and ammonium salts of the sulfosuccinate derivatives (Formula I) are obtained by reacting the appropriate alkali metal sulfite or bisulfite or ammonium sulfite or bisulfite with the corresponding maleic acid ester derivative of the carbohydrate. The maleic acid ester, in turn, is prepared by heating the particular carbohydrate with maleic anhydride in a suitable solvent medium such as toluene and, after solvent removal, purified by washing either with water or dilute mineral acid. The D.S. value is controlled by the ratio of maleic anhydride to starting carbohydrate used. In the cases where the maleic acid ester is water soluble, the product is purified by first dissolving in water and neutralizing to pH 8-8.6 with an alkali metal bicarbonate or carbonate, evaporating to dryness and then extracting with a lower alcohol (e.g. methanol or ethanol) to separate the desired product from maleate salts. Alternatively, an aqeuous solution or slurry of a sulfosuccinate salt, e.g. the disodium salt, may be acidified to about pH 4 with mineral acid and the acid salt thus formed (e.g. carbohydrate residue precipitated or extracted with a lower alcohol and then isolated by filtration or evaporation, respectively. An aqueous solution or slurry of the acid salt is then neutralized to a pH of -8-8.6 with the desired base: e.g. potassium hydroxide. sodium bicarbonate, lithium carbonate, ammonium hydroxide, tetramethylammonium hydroxide. monoethanolamine, diethanolamine, triethanolamine and morpholine to form the corresponding alkali metal, ammonium or substituted ammonium salts.
The preferred cations for use in the compositions of the present invention are alkali metal, alkanolammonium (i.e., mono-, diand tri-ethanolammonium), ammonium and mixtures thereof. Those especially preferred are sodium, potassium and triethanolammonium, although any cation which will solubilize the carbohydrate sulfosuccinates is suitable for use in the present invention.
Any carbohydrate, especially polysaccharides, containing hydroxy groups may be used as a starting material for forming the derivatives used in the present invention including such substances as the (C, to C.) alkyl glycosides, exemplified by methyl and ethyl glucopyranosides; disaccharides. exemplified by sucrose, lactose, maltose and cellobiose. trisaccharides such as raffinose; oligosaccharides, exemplified by those obtainable by enzymatic hydrolysis of corn starch and cellulose; polysaccharides, exemplified by glycogen, starches such as those derived from corn, potato, rice, arrowroot, tapioca, wheat, sago, etc., cellulose, hemicelluloses, polyuronic acids, dextrans, pectins, alginic acid and natural gums such as arabic and acacia as well as any of the aforementioned carbohydrates that may be modified by etherification, carboxymethylation or cross-linking. The preferred sulfosuccinate derivatives used in the composition of the present invention are the disodium sulfosuccinate ester derivatives of starch, hydrolyzed starch, cellulose and sucrose.
According to the present invention, excellent cleaning results can be obtained by using the builders described above with a wide range of detergent surface active materials and mixtures thereof. The builders can be used singularly, in combination with each other as the sole builder in the detergent composition or in combination with other builders such as sodium nitrilotriacetate, sodium ethylenediaminetetraacetate, sodium tripolyphosphate, sodium and potassium pyrophosphate, sodium polyacrylate, oxidized starches, trisodium citrate, trisodium carboxymethyloxysuccinate and alkali metal carbonates.
In the detergent compositions of the present invention, the only essential ingredients are the detergent surface active material and the builder. The weight percent of the builder present in the detergent compositions will range from about 5 to about 90% and preferably from about 20 to about 60% and more preferably 35-50% by weight of the total weight of the composition. When expressed as a weight ratio of builder to surfactant, the builders used in the instant invention will generally be present in a ratio of about 1:10 to about I0: I, and preferably 2:l-5:l depending on the end use or whether a heavy-duty or light-duty detergent is desired.
Similarly, in detergent compositions suitable for washing dishes in mechanical dishwashers, the ratio of builder to detergent may be as high as 50: l.
In addition to having detergent building properties, the sulfosuccinate derivatives of the polysaccharides described in the present invention may also be used as anti-redeposition agents in detergent compositions When used for such purposes, the sulfosuccinate polysaccharide derivative is generally present in minor amounts in relation to the total weight of the composition. For example, as a rule, when employed as an antiredeposition agent, the polysaccharide derivatives of the invention will generally comprise up to 5% (preferably l3%) of the total weight of the detergent composition.
The detergent surface active compounds which can be used in the compositions of this invention include anionic, nonionic, zwitterionic, ampholytic detergent compounds and mixtures thereof. These suitable substances are outlined at length below.
a. Anionic detergent compositions which can be used in the compositions of this invention include both soap and non-soap detergent compounds. Examples of suitable soaps are the sodium, potassium, ammonium and alkylol-ammonium salts of higher fatty acids (C -C Particularly useful are the sodium or potassium salts of the mixtures of fatty acids derived from coconut oil and tallow. i.c.. sodium or potassium tallow and coconut soap and tall oil soap. Examples of anionic organic nonsoap detergent compounds are the water soluble salts, alkali metal salts of organic sulfuric reaction products having in their molecular structure an alkyl radical containing from about 8 to about 22 carbon atoms and a radical selected from the group consisting of sulfonic acid and sulfuric acid ester radicals. (Included in the term alkyl is the alkyl portion of higher acyl radicals.) Important examples of the synthetic detergents which form a part of the compositions of the present invention are the sodium or potassium alkyl sulfates espe cially those obtained by sulfating the higher alcohols (C -C carbon atoms) produced by reducing the glycerides of tallow or coconut oil; sodium or potassium alkyl benzenesulfonates in which the alkyl group contains from about 9 to about carbon atoms and in which the benzene ring is attached to the alkyl chain at either the one position or at the secondary positions such as in sodium linear secondary (C -C mlkyl benzenesulfonate, sodium p-( 2-dodecyl )benzenesulfonate, sodium p-(2-octadecyl)benzenesulfonate, sodium p-(3-dodecyl)benzenesulfonate and 3-phenyldodecanesulfonate; sodium alkyl glyceryl ether sulfonates, especially those ethers of the higher. alcohols derived from tallow and coconut oil and synthetic alcohols derived from petroleum; sodium coconut oil fatty acid monoglyceride sulfates and sulfonates; sodium or potassium salts of sulfuric acid esters of the reaction product of one mole of a higher fatty alcohol (e.g., tallow or coconut oil alcohols) and about 1 to 6 moles of ethylene oxide per molecule and in which the alkyl radicals contain about 9 to about 18 carbon atoms; the reaction product of fatty acids esterified with isethionic acid and neutralized with sodium hydroxide where, for example, the fatty acids are derived from coconut oil; sodium or potassium salts of fatty acid amides of methyl taurine in which the fatty acids, for example, are derived from tallow; alkane sulfonates such as those derived by reacting alpha-olefins containing 8 to 20 carbon atoms with sodium bisulfite and those derived by reacting paraffins with S0 and Cl and then hydro- ]yzing with a base to produce a random sulfonate; alpha-olefin sulfonates such as those derived by reacting alpha-olefins with $0 and then neutralizing the reaction product; and others known in the art.
b. Nonionic synthetic detergents may be broadly defined as compounds which do not ionize in water solution. For example, a well-known class of nonionic synthetic detergents is made available on the market under the trade name of Pluronic. These compounds are formed by condensing ethylene oxide with an hydrophobic base formed by the condensation of propylene oxide with propylene glycol. The hydrophobic protion of the molecule which, of course, exhibits water insolubility has a molecular weight of from about 1,500 to 1,800. The addition of polyoxyethylene radicals to this hydrophobic portion tends to increase the water solubility of the molecule as a whole and the liquid character of the product is retained up to the point where polyoxyethylene content is about 50% of the total weight of the condensation product.
Other suitable nonionic synthetic detergents include:
I. The polyethylene oxide condensates of alkylphenols, e.g., the condensation products of alkylphenols having an alkyl group containing from about 6 to 12 carbon atoms in either a straight chain or branched chain configuration, with ethylene oxide, the said ethylene oxide being present in amounts equal to 5 to 25 moles of ethylene oxide per mole of alkylphenols. The alkyl substituent in such compounds may be derived from polymerized propylene, di-isobutylene, octene, dodecene or nonene, for example.
2. Those derived from the condensation of ethylene oxide with the product resulting from the reaction of propylene oxide and ethylenediamine. For examle, compounds containing from about 40% to about polyoxyethylene by weight and having a molecular weight of from about 5,000 to about 1 1,000 resulting from the reaction of ethylene oxide groups with a hydrophobic base constituted of the reaction product of ethylene diamine and excess propylene oxide, said hydrophobic base having a molecular weight of the order to 2,500 to 3,000, are satisfactory.
3. The condensation product of primary or secondary aliphatic alcohols having from 8 to 18 carbon atoms, in either straight chain or branched chain configuration, with ethylene oxide, e.g., a coconut alcohol-ethylene oxide condensate having from 3 to 30 moles of ethylene oxide per mole of coconut alcohol, the coconut alcohol fraction having from l0 to 14 carbon atoms; a random linearsecondary alcohol containing 1 ll 5 carbon atoms derived from n-paraffins and condensed with 3-20 moles of ethylene oxide per mole of the alcohol.
4. Long chain tertiary amine oxides corresponding to the following general formula, R,R R N 0, wherein R is an alkyl radical of from about 8 to 18 carbon atoms, and R and R are each methyl, ethyl or hydroxy ethyl radicals. The arrow in the formula is a conventional representation of a semi-polar bond. Examples of amine oxides suitable for use in this invention include dimethyldodecylamine oxide, dimethyloctylamine oxide, dimethyldecylamine oxide, dimethyltetradecylamine oxide and dimethylhexadecylamine oxide, N- bis( hydroxyethyl )dodecylamine oxide.
5. Long chain tertiary phosphine oxides corresponding to the following formula RR'R"P 0, wherein R is an alkyl, alkenyl or monohydroxyalkyl radical ranging from 10 to l8 carbon atoms in chain length and R and R" are each alkyl or monohydroxyalkyl groups containing from I to 3 carbon atoms. The arrow in the formula is a conventional representation of a semipolar bond. Examples of suitable phosphine oxides are:
6. Dialkyl sulfoxides corresponding to the following formula, RR'S 0, wherein R is an alkyl, alkenyl, betaor gamma-monohydroxyalkyl radical or an alkyl or betaor gamma-monohydroxyalkyl radical containing one or two other oxygen atoms in the chain, the R groups ranging from 10 to 18 carbon atoms in chain length, and wherein R is methyl, ethyl or alkylol. Examples of suitable sulfoxide compounds are:
dodecyl methyl sulfoxide, tetradecyl methyl sulfoxide,
3-hydroxytridecyl methyl sulfoxide, 2-hydroxydodecyl methyl sulfoxide, 3-hydroxy-4-decyloxybutyl methyl sulfoxide, 3-hydroxy-4-dodecyloxybutyl methyl sulfoxide, Z-hydroxy-3-decyloxypropyl methyl sulfoxide, dodecyl ethyl sulfoxide, 2-hydroxydodecyl ethyl sulfoxide, and dodecyl-Z-hydroxy ethyl sulfoxide.
c. Ampholytic synthetic detergents can be broadly described as derivatives of aliphatic secondary and tertiary amines, in which the aliphatic radical may be straight chain or branched and wherein one of the aliphatic substituents contains from about 8 to 18 carbon atoms and one contains an anionic water solubilizing group. Examples of compounds falling within this definition are sodium-3-dodecylaminopropionate and sodium-3-dodecylaminopropanesulfonate and sodium N-Z- hydroxydodecyl-N-methyl-taurate.
d. Zwitterionic synthetic detergents can be broadly described as derivatives of aliphatic quaternary ammonium compounds, sulfonium compounds and phosphonium compounds in which the aliphatic radical may be straight chain or branched and wherein one of the aliphatic substituents contains from about 8 to 18 carbon atoms and one contains an anionic water solubilizing group. Examples of compounds falling within this definition are 3-(N,N-dimethyl-N- hexadecylammonio)propanel -sulfonate, 3-(N,N- dimethyl-N-hexadecylammonio )-2-hydroxypropanel sulfonate, 3-(dodecylmethylsulfonium)propane sulfonate, and 3-(cetylmethylphosphonium )ethane sulfonate.
In addition to the essential ingredients in the detergent composition, other optional ingredients may also be added. Examples of the optional ingredients are perfumes, colorants, fabric softening agents, fungicides germicides, enzymes, fluorescent dyes antiredeposition agents, hydrotropes and in the case of liquid compositions, opacifiers and organic solvents. Other ingredients such as bleaches, i.e., sodium perborate with or without activators, active chlorine compounds and inorganic salts such as sodium carbonate, sodium bicarbonate, sodium sulfate, sodium chloride and sodium silicate may also be present.
The detergent compositions of the present invention can be utilized in washing solutions over a pH range of from about 7-l l and more preferably 8-10.
Example I and Table I further illustrate the present invention. The detergent formulations set forth in the Table represent detergent compositions containing an anionic surface active agent in combination with builders of the present invention and also standard phosphate builders. The compositions were prepared by blending together the recited components in the proportions indicated, including an anticorrosion agent and buffering agent (sodium silicate) and adjusting the indicated pH where necessary by the addition of sodium hydroxide. The compositions were then tested for detergency or cleaning ability in the Terg-O-Tometer test wherein washing conditions are as indicated and the results reported as detergency units. The average detergency units (DU) of the formulation is the final reflectance value of the washed cloth minus the initial reflectance of the soiled cloth (the average of two runs), the reflectance value being obtained by measurement with a Gardner automatic color difference meter.
EXAMPLE 1 Starch Sulfosuccinate Corn starch-maleic acid ester 10 g (0.04] mole) having a D.S. value of 0.80 is suspended in ml of water and the pH adjusted to about 7 with sodium carbonate. To this mixture is added 5.4 g (0.052 mole) of sodium bisulfite. After readjusting the pH to 7 the mixture is stirred for 1 hour at room temperature and then heated at 50C for 3 hours. The pH is then adjusted to 8.5 and starch sulfosuccinate having a D.S. value of 0.8 is obtained by precipitating the product with ethyl alcohol, decanting the liquid, washing the residue with additional ethyl alcohol and finally drying the residue obtained.
Sulfosuccinate derivatives of other carbohydrates may be afforded using the above procedure by substituting in place of corn starch-maleic acid ester the appropriate maleic acid ester of the desired di-, oligoor poly-saccharide or alkyl glycoside.
TABLE 1 DETERGENCY BUILDING PROPERTIES OF STARCH SULFOSUCCINATE formulation What is claimed is:
l. A sulfosuccinate derivative of a carbohydrate selected from the group consisting of an alkyl glycoside, a di-, oligoor poly-saccharide having the general formula wherein A is COO[H]M or CH OR; R is hydrogen or a sulfosuccinate moiety of the formula:
T 0 HOR OR H wherein R is as defined above; M is a cation selected from the group consisting of an alkali metal, alkanol ammonium or ammonium, or mixtures thereof; n is an integer from about ll0,000 and wherein the D5.
value, which represents the average number of sulfosuccinate moieties per monomeric unit, is at least 1 when n is l, and at least 0.5 per monomeric unit when n is greater than I.
2. The compound of claim 1 wherein the alkyl glycoside is selected from the group, methyl glucoside and ethyl glucoside, and the D5. value is from about 2 to about 4.
3. The compound of claim 1 wherein the disaccharide is selected from the group consisting of sucrose, lactose, maltose and cellobiose, and the D5 value is from about 1 to about 8.
4. The compound of claim 1 wherein the oligosaccharide is selected from the group consisting of a hydrolyzed starch and cellulose, and the D5. value is from about l to about 3.
5. The compound of claim 1 wherein the polysaccharide is selected from the group consisting of starch, cellulose, glycogen, hemicellulose, alginate, pectin and gum, and the D8. value is from about l to about 3.
|Cited Patent||Filing date||Publication date||Applicant||Title|
|US3103507 *||Feb 23, 1960||Sep 10, 1963||Chjoh|
|US3324108 *||Jun 29, 1964||Jun 6, 1967||Scholten Chemische Fab||Monosaccharide and oligosaccharide polyethers|
|US3772269 *||Jul 24, 1969||Nov 13, 1973||Ici America Inc||Glycoside compositions and process for the preparation thereof|
|US3808200 *||Jan 7, 1971||Apr 30, 1974||Agriculture||Hexitol,glucose and surcose esters of alpha-sulfo fatty acids|
|Citing Patent||Filing date||Publication date||Applicant||Title|
|US4379919 *||Apr 1, 1982||Apr 12, 1983||National Starch And Chemical Corporation||Starch sulfomaleate half-esters, a method for their preparation and their use to prepare starch disulfosuccinate half-esters|
|US4387221 *||Apr 1, 1982||Jun 7, 1983||National Starch And Chemical Corporation||Alkyl- and alkenyl-sulfosuccinate starchhalf-esters, a method for the preparation thereof|
|US5179201 *||May 3, 1991||Jan 12, 1993||Basf Aktiengesellschaft||Alkyl mono-and polyglucoside ether carboxylates, and their preparation and use thereof|
|US5238597 *||Feb 25, 1991||Aug 24, 1993||Hoechst Aktiengesellschaft||Sucrosetricarboxylic acid and compositions containing the same|
|US5415801 *||Aug 27, 1993||May 16, 1995||The Procter & Gamble Company||Concentrated light duty liquid or gel dishwashing detergent compositions containing sugar|
|US5474710 *||Aug 27, 1993||Dec 12, 1995||Ofosu-Asanta; Kofi||Process for preparing concentrated surfactant mixtures containing magnesium|
|US5898025 *||Aug 1, 1997||Apr 27, 1999||Henkel Kommanditgesellschaft Auf Aktien||Mildly alkaline dishwashing detergents|
|US8871699||Sep 13, 2012||Oct 28, 2014||Ecolab Usa Inc.||Detergent composition comprising phosphinosuccinic acid adducts and methods of use|
|US9023784||Aug 13, 2013||May 5, 2015||Ecolab Usa Inc.||Method of reducing soil redeposition on a hard surface using phosphinosuccinic acid adducts|
|EP0050015A2 *||Oct 9, 1981||Apr 21, 1982||Yuken Industries Co. Ltd.||Cleaning composition|
|EP0124367A2 *||Apr 27, 1984||Nov 7, 1984||Unilever N.V.||Detergent compositions|
|EP0280143A1 *||Feb 15, 1988||Aug 31, 1988||Henkel Kommanditgesellschaft auf Aktien||Liquid cleaning agent|
|U.S. Classification||536/2, 536/63, 536/3, 536/109, 536/115, 536/114, 536/4.1, 536/110|
|International Classification||C11D3/22, C08B3/00, C11D3/00, C08B37/00, C08B3/14, C08B31/00, C08B3/12, C08B31/04|
|Cooperative Classification||C08B3/12, C11D3/221, C08B37/00, C08B31/04, C08B3/14, C11D3/228|
|European Classification||C08B3/12, C08B3/14, C11D3/22B, C08B37/00, C08B31/04, C11D3/22E12|