Compositions comprising sugar amine and fatty acid

Information

  • Patent Grant
  • 10961484
  • Patent Number
    10,961,484
  • Date Filed
    Friday, October 7, 2016
    7 years ago
  • Date Issued
    Tuesday, March 30, 2021
    3 years ago
Abstract
What are described are compositions comprising a) one or more sugar amines of the formula (I) in which R1 and R2 are independently H, CH3 or 2-hydroxyethyl and/or one or more corresponding protonated sugar amines with the counterion R—COO— in which R is defined as R from the substances of component b) below, and b) one or more substances selected from the group consisting of fatty acids of the formula R—COOH, fatty acid salts of the formula R—COO-M+ and mixtures thereof, in which R is a linear or branched saturated alkyl radical having 11 to 21 carbon atoms or a linear or branched, mono- or polyunsaturated alkenyl radical having 11 to 21 carbon atoms and M+ is a counterion. The compositions described are very advantageous, for example, for production of liquid washing compositions, and of shower gels, liquid soaps or face cleansers. In addition, the sugar amines are advantageously suitable as neutralizing agents for fatty acids.
Description

The invention relates to compositions comprising one or more sugar amines and/or protonated sugar amines with fatty acid anions as counterions and one or more fatty acids and/or fatty acid salts, to the use of such compositions for producing liquid detergents or shower baths, liquid soaps or face cleansers, and to the use of the sugar amines as neutralizing agents for fatty acids. The invention furthermore relates to salts of sugar amines and fatty acids.


The use of sugar amines in detergents and cosmetics is already known from the prior art.


DE 42 38 211 C1 describes detergent mixtures comprising specific cationic sugar surfactants, for example derived from glucamines, and the use thereof for producing e.g. detergents and products for hair care and body care. The detergent mixtures are characterized inter alia by a high cold water solubility or cold water dispersibility and can be processed without problems to give highly concentrated, low viscosity solutions or dispersions.


DE 198 08 824 C1 discloses hair treatment compositions with a content of at least one polymer with acidic groups, such as e.g. carboxylic acid groups, and at least one N-unsubstituted or N-substituted polyhydroxyamine with at least four hydroxyl groups, such as e.g. glucamine, and moreover the use of at least one N-unsubstituted or N-substituted polyhydroxyamine with at least four hydroxyl groups in hair treatment compositions for the neutralization of polymers with acidic groups.


EP 1 676 831 A1 describes polyhydroxyalkylamines disubstituted on the nitrogen, such as e.g. N,N-dialkylglucamines, where both substituents each contain 2 to 30 carbon atoms. Furthermore, a large number of application possibilities for the polyhydroxyalkylamines disubstituted on the nitrogen is also disclosed, such as e.g. the use in aqueous liquid detergents or in shampoos, liquid body cleansing formulations, hair conditioning formulations and aqueous sunscreen formulations.


EP 1 529 832 A1 discloses metal working fluids comprising aminopolyols such as, for example, D-glucamine, methylglucamine, ethylglucamine or hydroxyethylglucamine. Moreover, it is described for example that aminopolyols and preferably amino sugars can be used e.g. as neutralizing and reaction component in coating compositions, cosmetics, physiological solutions and carrier substances for medicaments.


EP 614 881 describes the preparation of tertiary dialkylpolyhydroxyamines, such as e.g. dimethylglucamine.


Fatty acids and salts thereof (where the salts of the fatty acids are also referred to as “fatty acid soaps”) are highly valuable ingredients of detergents and cleaners. However, typical soap solutions are only homogeneous at a relatively high pH and are often relatively viscous and have inadequate solubility specifically at tendentially lower pH values.


It was therefore the object to provide novel compositions which produce low viscosity, homogeneous solutions of fatty acids or fatty acid soaps in aqueous compositions over a broad pH range and thus facilitate the incorporation of longer-chain fatty acids and/or fatty acid soaps in detergents and cleaners.


Surprisingly, it has now been found that this object is achieved by compositions comprising


a) one or more substances selected from the group consisting of sugar amines of the formula (I), protonated sugar amines of the formula (Ia) and mixtures thereof




embedded image



in which


R1 and R2, independently of one another, are H, CH3 or 2-hydroxyethyl and


R has the meaning of R from the substances of component b) below


and


b) one or more substances selected from the group consisting of fatty acids of the formula R—COOH, fatty acid salts of the formula R—COOM+ and mixtures thereof, in which


R is a linear or branched saturated alkyl radical having 11 to 21 carbon atoms or a linear or branched mono- or polyunsaturated alkenyl radical having 11 to 21 carbon atoms and


M+ is a counterion, preferably selected from the group consisting of NH4+, organic ammonium ions [HNR5R6R7]+, where R5, R6 and R7, independently of one another, can be a linear or branched saturated alkyl group having 1 to 22 carbon atoms, a linear or branched, mono- or polyunsaturated alkenyl group having 2 to 22 carbon atoms, a C6-C22-alkylamidopropyl group, a linear monohydroxyalkyl group having 2 to 10 carbon atoms or a linear or branched dihydroxyalkyl group having 3 to 10 carbon atoms, and where at least one of the radicals R5, R6 and R7 is not hydrogen, Li+, Na+, K+, ½Ca++, ½Mg++, ½Zn++ or % Al+++ and mixtures of these ions.


The invention therefore provides compositions comprising


a) one or more substances selected from the group consisting of sugar amines of the formula (I), protonated sugar amines of the formula (Ia) and mixtures thereof




embedded image



in which


R1 and R2, independently of one another, are H, CH3 or 2-hydroxyethyl and


R has the meaning of R from the substances of component b) below


and


b) one or more substances selected from the group consisting of fatty acids of the formula R—COOH, fatty acid salts of the formula R—COOM+ and mixtures thereof, in which


R is a linear or branched saturated alkyl radical having 11 to 21 carbon atoms or a linear or branched mono- or polyunsaturated alkenyl radical having 11 to 21 carbon atoms and


M+ is a counterion, preferably selected from the group consisting of NH4+, organic ammonium ions [HNR5R6R7]+, where R5, R6 and R7, independently of one another, can be a linear or branched saturated alkyl group having 1 to 22 carbon atoms, a linear or branched, mono- or polyunsaturated alkenyl group having 2 to 22 carbon atoms, a C6-C22-alkylamidopropyl group, a linear monohydroxyalkyl group having 2 to 10 carbon atoms or a linear or branched dihydroxyalkyl group having 3 to 10 carbon atoms, and where at least one of the radicals R5, R6 and R7 is not hydrogen, Li+, Na+, K+, ½Ca++, ½Mg++, ½Zn++ or % Al+++ and mixtures of these ions.


As already mentioned, the compositions according to the invention have the advantage for example that they produce homogeneous solutions of fatty acids or fatty acid salts in aqueous compositions that are of low viscosity over a broad pH range.


In the compositions according to the invention, the radical R in the protonated sugar amines of the formula (Ia) has the meaning of R from the substances of component b) of the compositions according to the invention. This means that the radical R in the protonated sugar amines of the formula (Ia) also then assumes the meaning of R from the substances of the component b) of the compositions according to the invention if R in the substances of component b) of the compositions according to the invention assumes preferred, particularly preferred, especially preferred meanings etc.


Preferably, the one or more substances of component a) of the compositions according to the invention is or are selected from the group consisting of dimethylglucamine, hydroxyethylmethylglucamine, dimethylglucammonium with the counterion R—COO, hydroxyethylmethylglucammonium with the counterion R—COO and mixtures thereof.


Dimethylglucammonium with the counterion R—COO is compounds of the formula (Ia) from component a) of the compositions according to the invention in which R1 and R2 are CH3.


Hydroxyethylmethylglucammonium with the counterion R—COO is compounds of the formula (Ia) from component a) of the compositions according to the invention in which one of the radicals R1 and R2 is CH3 and the other of these radicals is —CH2CH2—OH.


Particularly preferably, the one or more substances of component a) is or are selected from the group consisting of dimethylglucamine, dimethylglucammonium with the counterion R—COO and mixtures thereof.


Preferably, the counterion M+ of the fatty acid salts of the formula R—COOM+ from component b) of the compositions according to the invention is selected from the group consisting of NH4+, monoethanolammonium, diethanolammonium, triethanolammonium, methylpropanolammonium, Na+, K+ and mixtures of these ions and particularly preferably selected from the group consisting of Na+, K+ and mixtures of these ions.


Preferably, the one or more substances of component b) of the compositions according to the invention is or are selected from the group consisting of the fatty acids (R—COOH) lauric acid, myristic acid, palmitic acid, stearic acid, oleic acid, linolic acid, C16/C18 fatty acids, behenic acid and erucic acid, the salts of the specified fatty acids with M+ as counterion (R—COOM+) and mixtures thereof. The preferred embodiment of the invention just described is referred to hereinbelow as “embodiment A”.


Particularly preferably, the one or more substances of component b) of the compositions according to the invention is or are selected from the group consisting of C16/C18 fatty acids, the salts of C16/C18 fatty acids with M+ as counterion and mixtures thereof. The particularly preferred embodiment of the invention just described is referred to hereinbelow as “embodiment B”.


Especially preferably, the one or more substances of component b) of the compositions according to the invention is or are selected from the group consisting of oleic acid, the salts of oleic acid with M+ as counterion and mixtures thereof. The especially preferred embodiment of the invention just described is referred to hereinbelow as “embodiment C”.


In an extraordinarily preferred embodiment of the invention, the one or more substances of component a) of the compositions according to the invention is or are selected from the group consisting of dimethylglucamine, dimethylglucammonium with the counterion R—COO, in which R—COO corresponds to the oleic acid anion (or deprotonated oleic acid), and mixtures thereof, and the one or more substances of component b) of the compositions according to the invention is or are selected from the group consisting of oleic acid, the salts of oleic acid with M+ as counterion and mixtures thereof. The extraordinarily preferred embodiment of the invention just described is referred to hereinbelow as “embodiment D”.


In the embodiments A, B, C and D, M+ is a counterion, it preferably being selected from the group consisting of NH4+, organic ammonium ions [HNR5R6R7]+, where R5, R6 and R7, independently of one another, can be hydrogen, a linear or branched saturated alkyl group having 1 to 22 carbon atoms, a linear or branched, mono- or polyunsaturated alkyenyl group having 2 to 22 carbon atoms, a C6-C22-alkylamidopropyl group, a linear monohydroxyalkyl group having 2 to 10 carbon atoms or a linear or branched dihydroxyalkyl group having 3 to 10 carbon atoms, and where at least one of the radicals R5, R6 and R7 is not hydrogen, Li+, Na+, K+, ½Ca++, ½Mg++, ½Zn++ or % Al+++ and mixtures of these ions, it being particularly preferably selected from the group consisting of NH4+, monoethanolammonium, diethanolammonium, triethanolammonium, methylpropanolammonium, Na+, K+ and mixtures of these ions and it being especially preferably selected from the group consisting of Na+, K+ and mixtures of these ions.


Among the compositions according to the invention, preference is given to those in which component a) comprises one or more protonated sugar amines of the formula (Ia). In these preferred compositions according to the invention, the sugar amines of the formula (I) from component a) are only optionally present.


Among the compositions according to the invention, in a preferred embodiment of the invention, preference is given to those in which component b) comprises one or more fatty acids of the formula R—COOH. In these preferred compositions according to the invention, the fatty acid salts of the formula R—COOM+ from component b) are only optionally present. Among these preferred compositions according to the invention, in a particularly preferred embodiment of the invention, preference is in turn given to those in which component b) comprises no fatty acid salts of the formula R—COOM+.


Preferably, the compositions according to the invention comprise water.


The substances of the formula (Ia) from component a) and the substances of component b) of the compositions according to the invention are surfactants. In this connection, not only are the substances of the formula (Ia) and the fatty acid salts of the formula R—COOM+ from component b) of the compositions according to the invention anionic surfactants, but in the context of the present invention the fatty acids R—COOH of component b) of the compositions according to the invention are also considered to be anionic surfactants. By contrast, the substances of the formula (I) from component a) of the compositions according to the invention are not surfactants.


Besides the substances of the formula (Ia) from component a) and the substances of component b), the compositions according to the invention preferably comprise one or more further surfactants.


In the context of the present invention, such further surfactants are referred to as substances which reduce the surface tension of a liquid or the interfacial tension between two phases and facilitate or assist the formation of dispersions or emulsions. This means in particular that the term “surfactants” in the context of the present invention also include substances which are usually referred to as emulsifiers.


The further surfactants can advantageously be selected from the group consisting of nonionic surfactants, anionic surfactants, cationic surfactants, amphoteric surfactants and betaine surfactants.


The amount of surfactants present in the compositions according to the invention (including the substances of component b) and the substances of the formula (Ia) from component a) of the compositions according to the invention) is, based on the total weight of the compositions according to the invention, preferably from 0.01 to 60.0% by weight, particularly preferably from 1.0 to 40.0% by weight, especially preferably from 2.0 to 30.0% by weight and extraordinarily preferably from 3.0 to 15.0% by weight.


As further anionic surfactants, preference is given to (C10-C22)-alkyl ethercarboxylates, fatty alcohol sulfates such as e.g. lauryl sulfate, fatty alcohol ether sulfates such as e.g. lauryl ether sulfate (or laureth sulfate), alkylamidosulfates, alkylamidosulfonates, fatty acid alkylamide polyglycol ether sulfates, alkanesulfonates, hydroxyalkanesulfonates, olefinsulfonates, acyl esters of isethionates, α-sulfo fatty acid esters (methyl ester sulfonates), alkylbenzenesulfonates, preferably linear alkylbenzenesulfonates, alkylphenol glycol ether sulfonates, sulfosuccinates, sulfosuccinic acid half-esters, sulfosuccinic acid diesters, fatty alcohol phosphates, fatty alcohol ether phosphates, protein-fatty acid condensation products, alkyl monoglyceride sulfates, alkyl monoglyceride sulfonates, alkyl glyceride ether sulfonates, fatty acid methyltaurides, fatty acid sarcosinates, sulforicinoleates, acyl glutamates such as e.g. sodium cocoylglutamate and acyl glycinates. These compounds and mixtures thereof are used in the form of their water-soluble or water-dispersible salts, for example in the form of their sodium salts, potassium salts, magnesium salts, ammonium salts, monoethanolammonium salts, diethanolammonium salts and/or triethanolammonium salts, and the analogous alkylammonium salts.


The amount of anionic surfactants in the compositions according to the invention (including the substances of component b) and the substances of the formula (Ia) from component a) of the compositions according to the invention) is, based on the total weight of the compositions according to the invention, preferably from 0.1 to 30.0% by weight, particularly preferably from 0.2 to 20.0% by weight and especially preferably from 0.5 to 15.0% by weight.


Preferred cationic surfactants are quaternary ammonium salts such as di-(C8-C22)-alkyl-dimethylammonium chloride or bromide;

  • (C8-C22)-alkyldimethylethylammonium chloride or bromide;
  • (C8-C22)-alkyltrimethylammonium chloride or bromide, preferably cetyltrimethylammonium chloride or bromide;
  • (C10-C24)-alkyldimethylbenzylammonium chloride or bromide, preferably (C12-C10-alkyldimethylbenzylammonium chloride;
  • (C8-C22)-alkyldimethylhydroxyethylammonium chloride, phosphate, sulfate or lactate;
  • (C8-C22)-alkylamidopropyltrimethylammonium chloride or methosulfate;
  • N,N-bis(2-C8-C22-alkanoyloxyethyl)dimethylammonium chloride or methosulfate, and
  • N,N-bis(2-C8-C22-alkanoyloxyethyl)hydroxyethylmethylammonium chloride or methosulfate.


The amount of cationic surfactants in the compositions according to the invention is, based on the total weight of the compositions according to the invention, preferably from 0.1 to 10.0% by weight, particularly preferably from 0.5 to 7.0% by weight and especially preferably from 1.0 to 5.0% by weight.


As nonionic surfactants, preference is given to fatty alcohol ethoxylates (alkyl polyethylene glycols); alkylphenol polyethylene glycols; fatty amine ethoxylates (alkylaminopolyethylene glycols); fatty acid ethoxylates (acylpolyethylene glycols); polypropylene glycol ethoxylates (Pluronics®); fatty acid alkanolamides, (fatty acid amide polyethylene glycols); N-acyl-N-methylglucamines; sucrose esters; sorbitol esters and sorbitan esters and the polyglycol ethers thereof; C8-C22-alkyl polyglucosides.


The amount of nonionic surfactants in the compositions according to the invention is, based on the total weight of the compositions according to the invention, preferably from 1.0 to 20.0% by weight, particularly preferably from 2.0 to 10.0% by weight and especially preferably from 3.0 to 7.0% by weight.


Furthermore, the compositions according to the invention can comprise amphoteric surfactants. These can be described as derivatives of long-chain secondary or tertiary amines which have an alkyl group with 8 to 18 carbon atoms and in which a further group is substituted with an anionic group which imparts solubility in water, thus e.g. with a carboxyl group, sulfate group or sulfonate group. Preferred amphoteric surfactants are aminopropionates such as N—(C12-C18)-alkyl-β-aminopropionates and N—(C12-C18)-alkyl-β-iminodipropionates as alkali metal salts, monoalkylammonium salts, dialkylammonium salts or trialkylammonium salts, and lauroamphoacetate, in particular as sodium salt.


Suitable further surfactants are also amine oxides. These are oxides of tertiary amines with a long-chain group of 8 to 18 carbon atoms and two mostly short-chain alkyl groups having 1 to 4 carbon atoms. Preference is given here, for example, to the C10- to C18-alkyldimethylamine oxides and fatty acid amidoalkyldimethylamine oxides.


A further preferred group of surfactants are betaine surfactants, also called zwitterionic surfactants. These contain a cationic group, in particular an ammonium group, and an anionic group, which can be a carboxylate group, sulfate group or sulfonate group, in the same molecule. Suitable betaines are preferably alkylbetaines such as cocobetaine or fatty acid alkylamidopropylbetaines (or alkylamidopropylbetaines), for example cocoacylamidopropyldimethylbetaine (or cocoamidopropylbetaine).


The amount of amphoteric surfactants and/or betaine surfactants in the compositions according to the invention is, based on the total weight of the compositions according to the invention, preferably from 0.5 to 20.0% by weight and particularly preferably from 1.0 to 15.0% by weight.


In a preferred embodiment of the invention, the compositions according to the invention comprise one or more surfactants selected from the group consisting of lauryl sulfate, laureth sulfate, methyl ester sulfonate, cocoamidopropylbetaine, alkylbetaines such as cocobetaine, sodium cocoyl glutamate and lauroamphoacetate.


In a further preferred embodiment of the invention, the compositions according to the invention comprise one or more surfactants selected from the group consisting of alkylated ether sulfates with a linear or branched alkyl group having 8 to 30 carbon atoms or a linear or branched mono- or polysaturated alkenyl group having 8 to 30 carbon atoms, betaines and derivatives thereof, and mixtures thereof and especially preferably selected from the group consisting of alkylated ether sulfates with a linear or branched alkyl group having 12 to 22 carbon atoms, betaines and derivatives thereof, and mixtures thereof.


In a further preferred embodiment of the invention the compositions according to the invention comprise one or more further anionic surfactants besides the substances of the formula (Ia) from component a) and the substances of component b). Among these, the one or more further anionic surfactants is or are in turn preferably selected from the group consisting of alkyl or alkenyl polyglycol ether sulfate, preferably alkyl polyglycol ether sulfate, alkyl or alkenyl sulfate, preferably alkyl sulfate, methyl ester sulfonate, alkylbenzenesulfonate, acyl glutamate and mixtures thereof. In the one or more further anionic surfactants just mentioned, “alkyl” is preferably a linear or branched saturated alkyl group having 12 to 22 carbon atoms, “alkenyl” is a linear or branched mono- or polyunsaturated alkenyl group having 12 to 22 carbon atoms and “acyl” is a linear or branched saturated acyl group having 12 to 22 carbon atoms or a linear or branched mono- or polyunsaturated acyl group having 12 to 22 carbon atoms.


In a further preferred embodiment of the invention, the compositions according to the invention comprise one or more nonionic surfactants selected from the group consisting of alkyl or alkenyl ethoxylates, preferably alkyl ethoxylates, alkyl polyglucosides, acyl-N-methylglucamines, fatty acid alkanolamides such as, for example, coconut fatty acid monoethanolamide and mixtures thereof. In the one or more nonionic surfactants just mentioned, “alkyl” is preferably a linear or branched saturated alkyl group having 12 to 22 carbon atoms, “alkenyl” is a linear or branched mono- or polyunsaturated alkenyl group having 12 to 22 carbon atoms and “acyl” is a linear or branched saturated acyl group having 12 to 22 carbon atoms or a linear or branched mono- or polyunsaturated acyl group having 12 to 22 carbon atoms. The fatty acid groups preferably have acyl groups as just defined for “acyl”.


Preferably, the compositions according to the invention comprise, based on the total weight of the compositions according to the invention, 0.5 to 30% by weight, particularly preferably 0.5 to 20% by weight, especially preferably 1 to 15% by weight and extraordinarily preferably 1 to 10% by weight, of the one or more substances of component a).


Preferably, the compositions according to the invention comprise, based on the total weight of the compositions according to the invention, 0.5 to 30% by weight and particularly preferably 1 to 10% by weight of the one or more substances of component b).


Preferably, the molar ratio of component (i): component (ii) in the compositions according to the invention is from 5:1 to 1:5 and particularly preferably from 3:1 to 1:3, where in this connection component (i) consists of the one or more substances of component b) of the compositions according to the invention and the one or more anions RCOO of the one or more protonated sugar amines of the formula (Ia) from component a) of the compositions according to the invention, and component (ii) consists of the one or more sugar amines of the formula (I) from component a) of the compositions according to the invention and the one or more cations of the protonated sugar amines of the formula (Ia) from component a) of the compositions according to the invention.


In a particularly preferred embodiment of the invention, the molar ratio of component (i): component (ii) in the compositions according to the invention is from 5:1 to 1:1 and particularly preferably from 3:1 to 1:1, where in this connection component (i) consists of the one or more substances of component b) of the compositions according to the invention and the one or more anions RCOO of the one or more protonated sugar amines of the formula (Ia) from component a) of the compositions according to the invention, and component (ii) consists of the one or more sugar amines of the formula (I) from component a) of the compositions according to the invention and the one or more cations of the protonated sugar amines of the formula (Ia) from component a) of the compositions according to the invention.


In a further particularly preferred embodiment of the invention, the molar ratio of component (i): component (ii) in the compositions according to the invention is from 1:1 to 1:5 and especially preferably from 1:1 to 1:3, where in this connection component (i) consists of the one or more substances of component b) of the compositions according to the invention and the one or more anions RCOO of the one or more protonated sugar amines of the formula (Ia) from component a) of the compositions according to the invention, and component (ii) consists of the one or more sugar amines of the formula (I) from component a) of the compositions according to the invention and the one or more cations of the protonated sugar amines of the formula (Ia) from component a) of the compositions according to the invention.


Preferably, the compositions according to the invention have a pH of 7 to 11 and particularly preferably from 8 to 10.


The pH values of the compositions according to the invention are measured directly in the compositions using a Knick Portamess 911 single-rod measurement electrode after calibration with corresponding standard buffers. Calibration is performed at pH 4 with citric acid/sodium hydroxide solution/hydrochloric acid buffer and at pH 7 with disodium hydrogenphosphate, potassium dihydrogenphosphate buffer.


Preferably, the compositions according to the invention have a viscosity <500 mPas and particularly preferably <100 mPas.


The viscosities are measured using a Brookfield viscometer model DV II, the spindles from the spindle set RV at 20 revolutions/minute and 20° C. Spindles 1 to 7 from the spindle set RV are used. Under these measurement conditions, spindle 1 is selected for viscosities of at most 500 mPa·s, spindle 2 is selected for viscosities of at most 1000 mPa·s, spindle 3 for viscosities of at most 5000 mPa·s, spindle 4 for viscosities of at most 10 000 mPa·s, spindle 5 for viscosities of at most 20 000 mPa·s, spindle 6 for viscosities of at most 50 000 mPa·s and spindle 7 for viscosities of at most 200 000 mPa·s.


In a preferred embodiment of the invention, the compositions according to the invention are in the form of a liquid detergent and particularly preferably in the form of a highly concentrated liquid detergent.


In a further preferred embodiment of the invention, the compositions according to the invention are in the form of a shower bath, a liquid soap or a face cleanser.


Instead of compositions which are directly suitable for an end use, the compositions according to the invention can also be in the form of concentrates that can be used in particular for producing compositions for certain end uses. The concentrates just mentioned are referred to hereinbelow as “concentrates according to the invention”. Preferably, the amount of the one or more substances of component a) in the concentrates according to the invention, based on the total weight of the concentrates according to the invention, is from 10 to 40% by weight. Furthermore, the amount of the one or more substances of component b) in the concentrates according to the invention, based on the total weight of the concentrates according to the invention, is from 5 to 40% by weight.


The compositions according to the invention, in particular the concentrates according to the invention, are advantageously suitable for producing liquid detergents and preferably highly concentrated liquid detergents. The present invention therefore further provides the use of a composition according to the invention, in particular of a concentrate according to the invention, for producing liquid detergents and preferably highly concentrated liquid detergents.


The compositions according to the invention, in particular the concentrates according to the invention, are furthermore advantageously suitable for producing shower baths, liquid soaps or face cleansers. The present invention therefore further provides the use of a composition according to the invention, in particular of a concentrate according to the invention, for producing shower baths, liquid soaps or face cleansers.


Furthermore, the sugar amines of the formula (I) present in component a) of the compositions according to the invention are advantageously suitable as neutralizing agents for fatty acids and preferably for the fatty acids present in component b) of the compositions according to the invention. The present invention therefore also further provides the use of one or more sugar amines of the formula (I)




embedded image



in which R1 and R2, independently of one another, are H, CH3 or 2-hydroxyethyl, as neutralizing agents for fatty acids and preferably for one or more fatty acids of the formula R—COOH in which R is a linear or branched saturated alkyl radical having 11 to 21 carbon atoms or a linear or branched mono- or polyunsaturated alkenyl radical having 11 to 21 carbon atoms.


In the case of the use according to the invention as neutralizing agent, the one or more sugar amines of the formula (I) is or are preferably selected from the group consisting of dimethylglucamine, hydroxyethylmethylglucamine and mixtures thereof.


In the case of the use according to the invention as neutralizing agent, the sugar amine of the formula (I) is particularly preferably dimethylglucamine.


In the case of the use according to the invention as neutralizing agent, the one or more fatty acids of the formula R—COOH is or are preferably selected from the group consisting of lauric acid, myristic acid, palmitic acid, stearic acid, oleic acid, linolic acid, C16/C18 fatty acids, behenic acid, erucic acid and mixtures thereof.


In the case of the use according to the invention as neutralizing agent, the one or more fatty acids of the formula R—COOH is or are particularly preferably selected from the group consisting of C16/C18 fatty acids and mixtures thereof.


In the case of the use according to the invention as neutralizing agent, the fatty acid of the formula R—COOH is particularly preferably oleic acid.


In an extraordinarily preferred embodiment of the use according to the invention as neutralizing agent, the sugar amine of the formula (I) is dimethylglucamine and the fatty acid of the formula R—COOH is oleic acid.


In the case of the use according to the invention as neutralizing agent, the molar ratio of the one or more fatty acids of the formula R—COOH to the one or more sugar amines of the formula (I) is preferably from 5:1 to 1:5 and particularly preferably from 3:1 to 1:3.


The present invention also further provides the salts of the formula (Ia) as described for the compositions according to the invention.


The salts according to the invention are advantageously suitable as surfactants. Moreover, they have the advantage for example that they dissolve very readily in water.


The salts according to the invention are in particular the salts of the formula (Ia)




embedded image



in which


R1 and R2, independently of one another, are H, CH3 or 2-hydroxyethyl and


R is a linear or branched saturated alkyl radical having 11 to 21 carbon atoms or a linear or branched mono- or polyunsaturated alkenyl radical having 11 to 21 carbon atoms.


The salts of the formula (Ia) according to the invention are preferably selected from the group consisting of dimethylglucammonium with the counterion R—COO, hydroxyethylmethylglucammonium with the counterion R—COO and mixtures thereof.


Particularly preferably, the salts of the formula (Ia) according to the invention are selected from the group consisting of dimethylglucammonium with the counterion R—COO and mixtures thereof.


Preferably, the counterion R—COO in the salts of the formula (Ia) according to the invention is selected from the group consisting of the fatty acids lauric acid, myristic acid, palmitic acid, stearic acid, oleic acid, linolic acid, C16/C18 fatty acids, behenic acid and erucic acid, in each case in deprotonated form, and mixtures thereof.


Particularly preferably, the counterion R—COO in the salts of the formula (Ia) according to the invention is selected from the group consisting of C16/C18 fatty acids, in each case in deprotonated form, and mixtures thereof.


Particularly preferably, the counterion R—COO in the salts of the formula (Ia) according to the invention is oleic acid in deprotonated form.


Extraordinarily preferably, the salt of the formula (Ia) according to the invention is dimethylglucammonium with deprotonated oleic acid as counterion R—COO.


The invention is illustrated in more detail below by reference to examples, although these should not be interpreted as limiting. Unless explicitly stated otherwise, all percentages are percentages by weight (% by weight).


The dimethylglucamine used in the examples was obtained according to EP 614 881 from N-methylglucamine by reductive amination.







EXAMPLE 1

5 g of oleic acid were introduced into 95 g of water (two-phase) and admixed with increasing molar amounts of different neutralizing agents up to 100 mol % of neutralizing agent. During this, the viscosity was determined (Brookfield, 20° C., 20 revolutions per minute (rpm), spindle 1 or 2), the homogeneity of the resulting solution was observed and the pH was measured (see table 1).


The following values are listed in table 1 and the following abbreviations were used therein:


The upper number in the respective lines of table 1 gives the measured viscosity in mPa·s.


“T” means: the solution is two-phase.


“C” means: the solution is clear.


“H” means: the solution is homogeneous, but cloudy.


The lower number in the respective lines of table 1 gives the measured pH. Here, “n.d.” means not determined.









TABLE 1







neutralizing agents used and also viscosity, homogeneity and pH of prepared compositions

















Neutralizing












agent [mol %]
10
20
30
40
50
60
70
80
90
100




















Monoethanol-
10 
8
8
625
1060
870
540
28
600
825


amine
T
T
T
H
H
H
H
H
H
H


(comparison)
  7.3
  7.7
  7.7
7.7
7.7
8.7
8.7
9.2
9.3
9.5


Triethanolamine
4
6
104 
1440
1220
980
910
750
470
420


(comparison)
T
T
T
H
H
H
H
H
H
H



n.d.
n.d.
n.d.
n.d.
n.d.
n.d.
n.d.
n.d.
n.d.
n.d.


Aminomethyl-
6
6
9
560
535
183
70
160
2860
4200


propanol
T
T
T
H
H
H
H
H
H
C


(comparison)
n.d.
n.d.
n.d.
n.d.
n.d.
n.d.
n.d.
n.d.
n.d.
n.d.


Sodium
6
6
8
13
38
23
13
9
6
6


hydroxide
T
T
T
T
H
H
H
T
T
C


solution
  8.3
  8.3
  8.2
8.5
8.6
9.2
9.6
9.7
9.7
11.3


(comparison)


Dimethyl-
5
15 
25 
70
30
20
20
10
10
10


glucamine
T
H
H
H
H
H
H
H
H
C


(invention)
  7.1
  8.0
  8.1
8.1
8.5
8.9
8.8
8.9
8.8
8.8









It can be seen from the values in table 1 that in the case of neutralization of oleic acid with dimethylglucamine, low viscosity, homogeneous solutions result even at low degrees of neutralization. Homogeneous solutions are already obtained above a pH of 8.0.


FORMULATION EXAMPLES
Formulation Example 1
Highly Concentrated Liquid Detergent (“Heavy Duty Liquid”)
















Amount [%



Ingredient
by weight]



















Methyl ester sulfonate
6



Linear alkylbenzene-
3



sulfonate




Sodium lauryl ether
11



sulfate (2 EO)




Fatty acid (30% by
3



weight C12, 25% by




weight C14, 20% by




weight C16, 25% by




weight C18 unsaturated)




C12/C15 alkyl ethoxylate
15



(8 EO)




Water
51.5



Propylene glycol
2



Dimethylglucamine
2



Enzymes
0.7



Polycarboxylate
0.6



Sodium citrate
5



Borax
0.2



Sodium hydroxide




to pH 7.7










Formulation Example 2
Highly Concentrated Liquid Detergent (“Heavy Duty Liquid”)
















Amount [%



Ingredient
by weight]



















Linear alkylbenzene-
8



sulfonate




Sodium lauryl ether
9



sulfate (2 EO)




Fatty acid (30% by
5



weight C12, 20% by




weight C14, 15% by




weight C16, 5% by




weight C18 saturated,




30% by weight C18




unsaturated)




C12/C14 alkyl
8



ethoxylate (7 EO)




Water
48.5



Ethanol
2



Propylene glycol
6



Dimethylglucamine
5



Enzymes
2



Soil Release Polyester
0.7



Sodium citrate
5



Borax
0.8



Sodium hydroxide




to pH 8.5










Formulation Example 3
Highly Concentrated Liquid Detergent in Monodose Format (“Monodose Surfactant Capsule”)
















Amount [%



Ingredient
by weight]



















Linear alkylbenzene-
24



sulfonate




Fatty acid (30% by
23



weight C12, 20% by




weight C14, 15% by




weight C16, 5% by




weight C18 saturated,




30% by weight C18




unsaturated)




C10 alkyl
19



ethoxylate (10 EO)




Water
4



Ethanol
4



Propylene glycol
10



Dimethylglucamine
8



Enzymes
0.7



Complexing agent
0.5



Methylpropanediol
6.8



Sodium hydroxide




to pH 8.4










Formulation Example 4
Shower Bath/Liquid Soap
















Amount [%



Ingredient
by weight]



















Lauric acid
6



Myristic acid
4



Palmitic acid
2



Dimethylglucamine
5



Sodium cocoylglutamate
2



Cocamide MEA (coconut
3



fatty acid monoethanolamide)




Hydroxypropylmethylcellulose
0.2



Water
ad 100



pH with potassium




hydroxide solution to pH = 8.6










Formulation Example 5
Face Cleanser
















Amount [%



Ingredient
by weight]



















Lauric acid
6



Myristic acid
4



Palmitic acid
2



Dimethylglucamine
5



Sodium cocoylglutamate
2



Oleoylmethylglucamide
3



Hydroxypropylmethylcellulose
0.2



Water
ad 100



pH with potassium hydroxide




solution to pH = 8.5









Claims
  • 1. A composition comprising a) one or more substances selected from the group consisting of dimethylglucammonium compounds with the counterion R—COO−; hydroxyethylmethyl-glucammonium compounds with the counterion R—COO−; and mixtures thereof,
  • 2. The composition as claimed in claim 1, wherein the one or more substances of component a) are selected from the group consisting of dimethylglucammonium compounds with the counterion R—COO−, and mixtures thereof.
  • 3. The composition as claimed in claim 1, wherein the counterion M+ is selected from the group consisting of NH4+, monoethanolammonium, diethanolammonium, triethanolammonium, methylpropanolammonium, Na+, K+ and mixtures of these ions.
  • 4. The composition as claimed in claim 1, wherein the one or more substances of component b) are selected from the group consisting of lauric acid, myristic acid, palmitic acid, stearic acid, oleic acid, linolic acid, C16/C18 fatty acids, behenic acid, erucic acid, the salts of the specified fatty acids with M+ as counterion (R—COO−M+) and mixtures thereof.
  • 5. The composition as claimed in claim 1, wherein the one or more substances of component b) are selected from the group consisting of C16/C18 fatty acids, the salts of C16/C18 fatty acids with M+ as counterion and mixtures thereof.
  • 6. The composition as claimed in claim 1, wherein the one or more substances of component b) are selected from the group consisting of oleic acid, the salts of oleic acid with M+ as counterion and mixtures thereof.
  • 7. The composition as claimed in claim 1, wherein component b) comprises one or more fatty acids of the formula R—COOH and comprises no fatty acid salts of the formula R—COO−M+.
  • 8. The composition as claimed in claim 1, further comprising water.
  • 9. The composition as claimed in claim 1, further comprising one or more anionic surfactants besides the substances of component a) and the substances of component b).
  • 10. The composition as claimed in claim 9, wherein the one or more anionic surfactants are selected from the group consisting of alkyl- or alkenylpolyglycol ether sulfate, alkyl or alkenyl sulfate, methyl ester sulfonate, alkylbenzenesulfonate, acylglutamate and mixtures thereof.
  • 11. The composition as claimed in claim 1, further comprising one or more nonionic surfactants selected from the group consisting of alkyl or alkenyl ethoxylates, alkylpolyglucosides, acyl-N-methylglucamines, fatty acid alkanolam ides and mixtures thereof.
  • 12. The composition as claimed in claim 1, wherein it comprises, based on the total weight of the composition, 0.5 to 30% by weight, of the one or more substances of component a).
  • 13. The composition as claimed in claim 1, wherein it comprises, based on the total weight of the composition, 0.5 to 30% by weight of the one or more substances of component b).
  • 14. The composition as claimed in claim 1, wherein the composition has a pH of from 7 to 11.
  • 15. The composition as claimed in claim 1, wherein the composition has a viscosity <500 mPas.
  • 16. A liquid detergent comprising at least one composition as claimed in claim 1.
  • 17. A shower bath, a liquid soap or a face cleanser comprising at least one composition as claimed in claim 1.
  • 18. A method for producing a liquid detergent, comprising the step of adding at least one composition as claimed in claim 1, to a liquid detergent.
  • 19. A method for producing a shower bath, liquid soap or face cleanser comprising the step of adding at least one composition as claimed in claim 1, to the shower bath, liquid soap or face cleanser.
  • 20. The composition as claimed in claim 1, wherein M+ is selected from the group consisting of Li+, Na+, K+, ½ Ca++, ½ Mg++, ½ Zn++, ⅓ Al+++, NH4+, organic ammonium ions [HNR5R6R7]+, where R5, R6 and R7, independently of one another, can be a linear or branched saturated alkyl group having 1 to 22 carbon atoms, a linear or branched, mono- or polyunsaturated alkenyl group having 2 to 22 carbon atoms, a C6-C22-alkylamidopropyl group, a linear monohydroxyalkyl group having 2 to 10 carbon atoms or a linear or branched dihydroxyalkyl group having 3 to 10 carbon atoms, and where at least one of the radicals R5, R6 and R7 is not hydrogen, and mixtures thereof.
  • 21. The composition as claimed in claim 1, further comprising one or more substances selected from the group consisting of dimethylglucamine; hydroxyethylmethylglucamine; and mixtures thereof.
Priority Claims (1)
Number Date Country Kind
10 2015 219 651.8 Oct 2015 DE national
PCT Information
Filing Document Filing Date Country Kind
PCT/EP2016/074085 10/7/2016 WO 00
Publishing Document Publishing Date Country Kind
WO2017/060481 4/13/2017 WO A
US Referenced Citations (183)
Number Name Date Kind
2016962 Flint Oct 1935 A
2667478 Schwartz Jan 1954 A
2703798 Schwartz Mar 1955 A
2891052 Boettner Jun 1959 A
2982737 Boettner May 1961 A
2993887 Zech Jul 1961 A
3002923 Barker Oct 1961 A
3272795 Jason Sep 1966 A
4079078 Collins Mar 1978 A
4341559 Friedemann Jul 1982 A
4400196 Albrecht Aug 1983 A
4413087 Bernot Nov 1983 A
4481186 Deckner Nov 1984 A
4505827 Rose Mar 1985 A
4565647 Llenado Jan 1986 A
4654207 Preston Mar 1987 A
4681946 Baur Jul 1987 A
4981684 MacKenzie Jan 1991 A
5009814 Kelkenberg Apr 1991 A
5194639 Connor Mar 1993 A
5254281 Pichardo Oct 1993 A
5298195 Brumbaugh Mar 1994 A
5317047 Sabate May 1994 A
5354425 Mackey Oct 1994 A
5449770 Shumate Sep 1995 A
5454982 Murch Oct 1995 A
5500155 Weuthen Mar 1996 A
5539134 Strecker Jul 1996 A
5559078 Garst Sep 1996 A
5560873 Chen Oct 1996 A
5625098 Kao Apr 1997 A
5691299 Fabry Nov 1997 A
5711899 Kawa Jan 1998 A
5712235 Nieendick Jan 1998 A
5716922 Curry Feb 1998 A
5750748 Boutique May 1998 A
5766267 Schumacher Jun 1998 A
5777165 Kao Jul 1998 A
5789372 Fabry Aug 1998 A
5874096 Hazen Feb 1999 A
5945389 Richard Aug 1999 A
6147045 Lappas Nov 2000 A
6147124 Ansmann Nov 2000 A
6165955 Chen Dec 2000 A
6264961 Ansmann Jul 2001 B1
6274126 Newell Aug 2001 B1
6288023 Honda Sep 2001 B1
6329331 Aronson Dec 2001 B1
6350788 Herold Feb 2002 B1
6391962 Zerrer May 2002 B2
6455001 Knappe Sep 2002 B1
6635708 Papenfuhs Oct 2003 B1
6727217 Nieendick Apr 2004 B1
6887838 Dykstra May 2005 B2
6903057 Tsaur Jun 2005 B1
7056379 Nieendick Jun 2006 B2
7217752 Schmucker-Castner May 2007 B2
7250392 Leonard Jul 2007 B1
7297666 Kuepper Nov 2007 B2
7380606 Pursley Jun 2008 B2
7407667 Zerrer Aug 2008 B2
7578995 Frantz Aug 2009 B2
7776318 Bissey-Beugras Aug 2010 B2
7820771 Lapra Oct 2010 B2
7872036 Toriyabe Jan 2011 B2
7897543 Bretschneider Mar 2011 B2
7998911 Berger Aug 2011 B1
8084452 Jeschke Dec 2011 B2
8178481 Sans May 2012 B2
8220564 Runquist Jul 2012 B2
8263538 Tsaur Sep 2012 B2
8324390 Fischer Dec 2012 B2
8404855 Jeschke Mar 2013 B2
8536340 Hamamoto Sep 2013 B2
8637432 Baur Jan 2014 B2
8729323 Kothandaraman May 2014 B2
8759255 Wacker Jun 2014 B2
8809547 Bretschneider Aug 2014 B2
8901041 Frisch Dec 2014 B2
9187407 Koshti Nov 2015 B2
9504636 Klug Nov 2016 B2
9949909 Klug Apr 2018 B2
10172774 Klug Jan 2019 B2
10265253 Klug Apr 2019 B2
20010023298 Weinelt Sep 2001 A1
20010056048 Bertolosso Dec 2001 A1
20020004476 Pancheri Jan 2002 A1
20020040662 Dietz Apr 2002 A1
20020065198 Highsmith May 2002 A1
20020168417 Blease Nov 2002 A1
20030004929 Julian Jan 2003 A1
20030049292 Turowski-Wanke Mar 2003 A1
20030069153 Jordan Apr 2003 A1
20030199403 Wells Oct 2003 A1
20040086470 Nieendick May 2004 A1
20050037926 Zerrer Feb 2005 A1
20050037942 Otterson Feb 2005 A1
20050172859 Nieendick Aug 2005 A1
20050233935 Gunn Oct 2005 A1
20060058205 Ainger Mar 2006 A1
20060079414 Nieendick Apr 2006 A1
20060089294 Depoot Apr 2006 A1
20060100127 Meier May 2006 A1
20060110415 Gupta May 2006 A1
20060110432 Luu May 2006 A1
20060135382 Molenda Jun 2006 A1
20060142291 Beilfuss Jun 2006 A1
20060166826 Zerrer Jul 2006 A1
20060171979 Calvo Aug 2006 A1
20070054820 Harichian Mar 2007 A1
20070060489 Sun Mar 2007 A1
20070110700 Wells May 2007 A1
20070128144 Bonastre Gilabert Jun 2007 A1
20070190004 Bockmuhl Aug 2007 A1
20070213226 Sieverding Sep 2007 A1
20080057014 Masuda Mar 2008 A1
20080317960 Pitt Dec 2008 A1
20090023622 Leidreiter Jan 2009 A1
20090042749 Meier Feb 2009 A1
20090111847 Li Apr 2009 A1
20090118152 Lam May 2009 A1
20090124498 Von Deyn May 2009 A1
20090253612 Mushock Oct 2009 A1
20090257972 Dieker Oct 2009 A1
20100051200 Mueller Mar 2010 A1
20100285077 Lintner Nov 2010 A1
20100326320 Swedo Dec 2010 A1
20110002865 Fournial Jan 2011 A1
20110146536 Tomlinson Jun 2011 A1
20110150786 Desenne Jun 2011 A1
20110152150 Bernard Jun 2011 A1
20110177945 Klingelhoefer Jul 2011 A1
20110251116 Aehle Oct 2011 A1
20110263471 Barnhart Oct 2011 A1
20120009127 Dasgupta Jan 2012 A1
20120010113 Hee Jan 2012 A1
20120070388 Man Mar 2012 A1
20120073817 Van Zanten Mar 2012 A1
20120094890 Anantaneni Apr 2012 A1
20120172223 Wacker Jul 2012 A1
20120244092 Moser Sep 2012 A1
20130030197 Harichian Jan 2013 A1
20130189212 Jawale Jul 2013 A1
20130216491 Ogihara Aug 2013 A1
20140096969 Ali Apr 2014 A1
20140135245 Annaheim May 2014 A1
20140230841 Mathonneau Aug 2014 A1
20140255330 Cron Sep 2014 A1
20140303389 Crosby Oct 2014 A1
20150032003 Cho Jan 2015 A1
20150125415 Klug May 2015 A1
20150126424 Klug May 2015 A1
20150126616 Klug May 2015 A1
20150133560 Klug May 2015 A1
20150140048 Klug May 2015 A1
20150141466 Klug May 2015 A1
20150141508 Klug May 2015 A1
20150150767 Klug Jun 2015 A1
20150164755 Klug Jun 2015 A1
20150164756 Klug Jun 2015 A1
20150282478 Baur Oct 2015 A1
20150320037 Wacker Nov 2015 A1
20150335550 Koshti Nov 2015 A1
20160074310 Klug Mar 2016 A1
20160136072 Klug May 2016 A1
20160143828 Klug May 2016 A1
20160243014 Dahms Aug 2016 A1
20160272666 Klug Sep 2016 A1
20160361243 Klug Dec 2016 A1
20170000710 Klug Jan 2017 A1
20170002297 Klug Jan 2017 A1
20170044434 Baur Feb 2017 A1
20170055524 Baur Mar 2017 A1
20170071199 Baur Mar 2017 A1
20170101606 Klug Apr 2017 A1
20170218293 Klug Aug 2017 A1
20170226349 Kupfer Aug 2017 A1
20170265477 Baur Sep 2017 A1
20170292062 Wylde Oct 2017 A1
20170305838 Appel Oct 2017 A1
20180215879 Kupfer Aug 2018 A1
20180291208 Kupfer Oct 2018 A1
20190076344 Klug Mar 2019 A1
Foreign Referenced Citations (192)
Number Date Country
2117007 Sep 1994 CA
1333226 Nov 1994 CA
2127644 Jan 1995 CA
1061960 Jun 1992 CN
1077489 Oct 1993 CN
1078746 Nov 1993 CN
1088258 Jun 1994 CN
1140987 Jan 1997 CN
1141653 Jan 1997 CN
1155239 Jul 1997 CN
1184417 Jun 1998 CN
1292641 Apr 2001 CN
1296524 May 2001 CN
1501772 Jun 2004 CN
1518408 Aug 2004 CN
1594518 Mar 2005 CN
100528887 May 2006 CN
1997341 Jul 2007 CN
101056959 Oct 2007 CN
102186340 Sep 2011 CN
102595882 Jul 2012 CN
103468362 Dec 2013 CN
103468382 Dec 2013 CN
104918490 Sep 2015 CN
1956509 May 1971 DE
2226872 Dec 1973 DE
4238211 Jan 1994 DE
4235783 Apr 1994 DE
4435383 Nov 1995 DE
19507531 Sep 1996 DE
19701127 Jul 1998 DE
19808824 Oct 1999 DE
19846429 Apr 2000 DE
19916090 Oct 2000 DE
10117993 Oct 2002 DE
10130357 Jan 2003 DE
102007034438 Jan 2009 DE
202013011412 Jan 2014 DE
202013011413 Jan 2014 DE
102012021647 May 2014 DE
0039860 Nov 1981 EP
0048436 Mar 1982 EP
0285768 Oct 1988 EP
0285786 Oct 1988 EP
0336151 Oct 1989 EP
0378985 Jul 1990 EP
0407874 Jan 1991 EP
0412849 Feb 1991 EP
0539588 May 1993 EP
0550637 Jul 1993 EP
0572723 Dec 1993 EP
0614881 Sep 1994 EP
0633244 Jan 1995 EP
0709449 May 1996 EP
0745719 Dec 1996 EP
0769548 Apr 1997 EP
0774503 May 1997 EP
0995994 Apr 2000 EP
1043017 Oct 2000 EP
1078978 Feb 2001 EP
1093722 Apr 2001 EP
1110944 Jun 2001 EP
1177223 Feb 2002 EP
1379129 Jan 2004 EP
1422288 May 2004 EP
1529832 May 2005 EP
1676831 Jul 2006 EP
1716842 Nov 2006 EP
S4810053 Feb 1973 JP
S63270534 Nov 1988 JP
H06501731 Feb 1994 JP
H06501733 Feb 1994 JP
H06240599 Aug 1994 JP
H07507341 Aug 1995 JP
H0812993 Jan 1996 JP
H0848618 Feb 1996 JP
H09502476 Mar 1997 JP
H09506683 Jun 1997 JP
H09510956 Nov 1997 JP
H10501279 Feb 1998 JP
H10508043 Aug 1998 JP
H11505839 May 1999 JP
H11246890 Sep 1999 JP
H11512334 Oct 1999 JP
2000512286 Sep 2000 JP
2000297028 Oct 2000 JP
2001501635 Feb 2001 JP
2001131579 May 2001 JP
2001247528 Sep 2001 JP
2002542344 Dec 2002 JP
2006183030 Jul 2006 JP
2006183039 Jul 2006 JP
2007538023 Dec 2007 JP
2008110953 May 2008 JP
2010018586 Jan 2010 JP
2010037252 Feb 2010 JP
2013534232 Sep 2013 JP
2014532815 Dec 2014 JP
2015518026 Jun 2015 JP
2017526776 Sep 2017 JP
9205764 Apr 1992 WO
9206073 Apr 1992 WO
9206154 Apr 1992 WO
9206158 Apr 1992 WO
9206161 Apr 1992 WO
9206162 Apr 1992 WO
9318125 Sep 1993 WO
9319149 Sep 1993 WO
9410130 May 1994 WO
9412608 Jun 1994 WO
9412609 Jun 1994 WO
9419941 Sep 1994 WO
9516824 Jun 1995 WO
9517880 Jul 1995 WO
9519415 Jul 1995 WO
9523840 Sep 1995 WO
9533033 Dec 1995 WO
9533035 Dec 1995 WO
9603974 Feb 1996 WO
9610386 Apr 1996 WO
9614374 May 1996 WO
9616540 Jun 1996 WO
9628023 Sep 1996 WO
9637589 Nov 1996 WO
9637592 Nov 1996 WO
9747284 Dec 1997 WO
9800496 Jan 1998 WO
9841601 Sep 1998 WO
9856496 Dec 1998 WO
9951716 Oct 1999 WO
0065014 Nov 2000 WO
0137658 May 2001 WO
0160877 Aug 2001 WO
02089575 Nov 2002 WO
2002096882 Dec 2002 WO
03000055 Jan 2003 WO
2003106457 Dec 2003 WO
2004056358 Jul 2004 WO
2004099150 Nov 2004 WO
2004099160 Nov 2004 WO
2005035486 Apr 2005 WO
2005063094 Jul 2005 WO
2005077934 Aug 2005 WO
2005117580 Dec 2005 WO
2006043635 Apr 2006 WO
2006056433 Jun 2006 WO
2006089633 Aug 2006 WO
2006100288 Sep 2006 WO
2007040280 Apr 2007 WO
2007057407 May 2007 WO
2007075459 Jul 2007 WO
2007101369 Sep 2007 WO
2007115643 Oct 2007 WO
2007115644 Oct 2007 WO
2007115646 Oct 2007 WO
2007141066 Dec 2007 WO
2007147500 Dec 2007 WO
2007149134 Dec 2007 WO
2005085216 Jan 2008 WO
2008009360 Jan 2008 WO
2008066153 Jun 2008 WO
2008067911 Jun 2008 WO
2008104503 Sep 2008 WO
2009002956 Dec 2008 WO
2009029561 Mar 2009 WO
2009049851 Apr 2009 WO
2009158478 Dec 2009 WO
2010005692 Jan 2010 WO
2010006713 Jan 2010 WO
2010069502 Jun 2010 WO
2010074747 Jul 2010 WO
2010074751 Jul 2010 WO
2010126657 Nov 2010 WO
2010138661 Dec 2010 WO
2011138450 Nov 2011 WO
2012061991 May 2012 WO
2012116939 Sep 2012 WO
2013016270 Jan 2013 WO
2013178668 Dec 2013 WO
2013178670 Dec 2013 WO
2013178671 Dec 2013 WO
2013178679 Dec 2013 WO
2013178697 Dec 2013 WO
2013178700 Dec 2013 WO
2013178701 Dec 2013 WO
2014056561 Apr 2014 WO
2014067663 May 2014 WO
2014170025 Oct 2014 WO
2015082062 Jun 2015 WO
2015124302 Aug 2015 WO
2016023693 Feb 2016 WO
2016041823 Mar 2016 WO
Non-Patent Literature Citations (59)
Entry
“Product Specification: N-octanoyl-N-methylglucamine”,Jun. 29, 2000 (Jun. 29, 2000), pp. 1-1, XP055098500, Retrieved from the Internet: URL:http://www.sigmaaldrich.com/Graphics/COfAInfo/SigmaSAPQM/SPEC/03/03129/03129 -BULKSIGMA.pdf.
Bezard (Lipids 1971;6:630-634).
Dale et al. (J. Sci. Food. Agric. 1955;6:166-170) (Year: 1955).
English Translation of Cited Excerpts of CN103468382A, Dec. 25, 2013. 2 pages.
European Coatings Journal in 2009, vol. 07, pp. 26-28.
Friedrich Vogel: “Kosmetik aus der Sicht des Chemikers”, Chemie in Unserer Zeit, No. 5, Jan. 1, 1986, pp. 156-164, XP055109030, DOI: 10.1002/ciuz.19860200504, p. 160.
Hardcopy of http://igf-bingen.de/Croda_produkte.pdf, Dec. 1, 2016. 3 pages.
International Preliminary Report on Patentability for PCT/EP2013/061044, dated Feb. 12, 2014. 7 pages.
International Preliminary Report on Patentability for PCT/EP2014/001723, dated Jun. 8, 2015. 16 pages.
International Preliminary Report on Patentability for PCT/EP2015/000443, dated Jan. 22, 2016. 6 pages.
International Preliminary Report on Patentability for PCT/EP2015/076072, dated May 16, 2017. 5 pages.
International Preliminary Report on Patentability for PCT/EP2016/071750, dated Apr. 10, 2018, 5 pages.
International Search Report for PCT/EP2013/003290, dated Feb 10, 2014. 5 pages.
International Search Report for PCT/EP2013/061044, dated May 15, 2014. 2 pages.
International Search Report for PCT/EP2013/061047, dated May 22, 2014. 3 pages.
International Search Report for PCT/EP2013/061075, dated May 15, 2014. 2 pages.
International Search Report for PCT/EP2013/061076, dated May 15, 2014, 2 pages.
International Search Report for PCT/EP2013/061100, dated Jul. 16, 2014. 4 pages.
International Search Report for PCT/EP2013/061100, dated Jul. 15, 2014. 4 pages.
International Search Report for PCT/EP2014/001722, dated Jan. 5, 2015. 3 pages.
International Search Report for PCT/EP2014/001723, dated Jan. 5, 2015. 3 pages.
International Search Report for PCT/EP2015/000443, dated Jun. 2, 2015. 2 pages.
International Search Report for PCT/EP2015/000871 dated Jul. 15, 2015. 3 pages.
International Search Report for PCT/EP2015/072453, dated Oct. 23, 2015. 2 pages.
International Search Report for PCT/EP2015/076072, dated Feb. 29, 2016. 2 pages.
International Search Report for PCT/EP2016/063433, dated Aug. 24, 2016. 2 pages.
International Search Report for PCT/EP2016/071750, dated Jan. 28, 2017, 3 pages.
International Search Report for PCT/EP2016/074085, dated Jan. 3, 2017, 3 pages.
Lichtenthaler, F.W., “Carbohydrates as Organic Raw Materials,” in Ullmann's Encyclopedia of Industrial Chemistry, Wiley-VCH Verlag, 2010. (34 pages).
Palm fatty acid distillate (PFAD) [online] retrieved on May 21, 2018 from: https://www.neste.com/corporate-info/sustainability/sustainable-supply-chain/pfa d-residue-palm-oil-refining-process; 1 page (Year: 2018).
Plante et al. Castor Oil [online] retrieved on Jan. 13, 2016 from: http://www.dionex.com/en-us/webdocs/110518-PO-UHPLC-Castor-Oil-31May2011-LPN2822 -01.pdf; 5 pages.
PubChem, Methylmeglumine, 2006. (Year: 2006) 9 pages.
Quack, et al., Fette-Seifen-Anstrichmittel 78, 200(1976) 7 pages.
R. Mohammadi, J. Wassink, A. Amirfazli, “Effect of Surfactants on Wetting of Super-Hydrophobic Surfaces”, Langmuir, American Chemical Society, (Oct. 1, 2004), vol. 20, No. 22, doi:10.1021/la049268k, ISSN 07437463, pp. 9657-9662, XP055098502.
Smith, J.T. et al., “Micellar Electrokinetic Capillary Chromatography with in Situ Charged Micelles. 1. Evaluation of N-D-Gluco-N-methylalkanamide Surfactants as Anionic Borate Complexes,” Anal. Chem. 1994, 66, 1119-1133.
Söderlind, E. et al., “The usefulness of sugar surfactants as solubilizing agents in parenteral formulations,” Elsevier, I nternational IJournal of Pharmaceutics 252 (2003) pp. 61-71, Aug. 19, 2002.
Study on Synthesis and Properties of “Green” Surfactants—Glucamine derivates, Zhao Handong, Master Thesis, Southern Yangtze University, pp. 5-6, Jul. 25, 2007.
Synergen OS Innovation Spotlight, Sep. 1, 2013, 5 pages.
Tan et al. (Appl Microbiol Biotechnol. 47:207-211) (Year: 1997).
Tegeler, T. et al., Special Guest Editor Section: Electrically Driven Microseparation Methods for Pesticides and Metabolites: I. Micellar Electrokinetic Capillary Chromatography of Carbamate Insecticides with MEGA-Borate and SDS Surfactants, Journal of AOAC International, vol. 82, No. 6, pp. 1542-1549, Nov. 6, 1999.
The Chemistry of Coconut Oil, accessed online Jul. 12, 2018 (Year: 2018) 5 pages.
V. Bergeron, P. Cooper, C. Fischer. J. Giermanska-Kahn, D. Langevin, and A. Pouchelon, “Polydimethylsiloxane (PDMS)-based antifoams” Colloids and Surfaces A: Physicochemical and Engineering Aspects 122 (1997) 103-120. 18 pages.
Walter, A. ; Suchy, S.E. ; Vinson, P.K., “Solubility properties of the alkylmethylglucamide surfactants”, Biochimica et Biophysica Acta (BBA)—Biomembranes, Elsevier, Amsterdam, NL, Amsterdam, NL, (Nov. 2, 1990), vol. 1029, No. 1, doi:10.1016/0005-2736(90)90437-S, ISSN 0005-2736, pp. 67-74, XP023354648.
Zhu, Y-P, et al., “Surface Properties of N-Alkanoyl-N-Methy Glucamines and Related Materials”, J. of Surfactants and Detergents, vol. 2, No. 3, Jul. 1, 1999. 6 pages.
“Phase behavior studies of quaternary systems containing N-lauroyl-N-methylglucamide/alcohol/alkane/water”, Yang et. al., Journal of Colloid and Interface Science, Academic Press, New York, NY, US, vol. 320, No. 1, Feb. 19, 2008, pp. 283-289 (Year: 2008).
Anan Yaghmur et al., Langmuir, vol. 19, No. 4, pa 1063-1068, Feb. 1, 2003.
Bouton et al, Langmuir, vol. 26, No. 11, pp. 7962-7966, Jun. 1, 2010.
Eliana Areanas et al: Langmuir, vol. 12, No. 2, pp. 588-590, Jan. 1, 1996.
Gregory J. McFann et al, Langmuir, vol. 9, No. 11, pp. 2942-2948, Nov. 1, 1993.
Howard, et al., “Comparison of Flowback Aids: Understanding Their Capillary Pressure and Wetting Properties”, SPE Paper 122307, 2009, 16 pages.
International Preliminary Report on Patentability for PCT/EP2015/070567, dated Dec. 23, 2016, 12 pages.
International Search Report for PCT/EP2015/070567, dated Mar. 22, 2016, 5 pages.
Panga, et al., “Wettability Alteration for Water-Block Prevention in High-Prevention in High-Temperature Gas Wells”, SPE Paper 100182, 2006, 13 pages.
Penny, et al., “Field Studies of Drilling and Completion Fluids to Minimize Damage and Enhance Gas Production in Unconventional Reservoirs”, SPE Paper 107844, 2007, 11 pages.
Pursley, et al., “Microemulsion Additive Enable Optimized Formation Damage Repair and Prevention” Paper 86556, 2004, SPE, 7 pages.
Quintero, et al., “Proper Design Criteria of Microemulsion Treatment fluids for Enhancing Well Production”, SPE 144451, 2012, 10 pages.
Rickman, et al., “Optimizing Microemulsion/surfactant Packages for Shale and Tight-Gas Reservoirs”, Paper 131107, 2010, SPE, 7 pages.
S. Ezrahi et al., Journal of Colloid and Interface Science, vol. 191, No. 2, pp. 277-290, Jul. 1, 1997.
S. Ray et al., Langmuir, vol. 10, No. 8, pp. 2511-2515, Aug. 1, 1994.
Related Publications (1)
Number Date Country
20180282664 A1 Oct 2018 US