FIELD OF THE INVENTION

The present invention relates to a liquid detergent composition which provides improved grease removal from hard surfaces including plastic and improved rinse feel.

BACKGROUND OF THE INVENTION

The detergent formulator is constantly aiming to improve the performance of detergent compositions. One of the biggest challenges encountered in hard surface cleaning is the removal of greasy soils, in particular the removal of greasy soils from dishware including hydrophobic items such as plastic.

In manual dishwashing, the challenge is not only to remove the grease from hydrophobic items but also to provide a good feeling during the rinse. Sometimes items can feel greasy or slippery during the rinse and this is disliked by users.

Accordingly, there is a need for a liquid detergent composition that provides good grease removal from dishware and at the same time does leave dishware free from slippery feeling during rinse.

SUMMARY OF THE INVENTION

The present invention addresses this need by providing a liquid detergent composition comprising a specific surfactant system and a specific cleaning amine. The detergent composition is preferably a hand dishwashing detergent composition. The surfactant system comprises an anionic surfactant and a primary co-surfactant in a specific weight ratio and optionally but preferably a secondary co-surfactant. The primary co-surfactant is selected from the group consisting of amphoteric surfactant, zwitteronic surfactant and mixtures thereof. The weight ratio of anionic surfactant to primary co-surfactant is less than about 2.5: 1, preferably more than about 1: 1.

One advantage of the present invention is that it does not provide slippery feeling on washed items and provide very efficient grease removal. Specially preferred anionic surfactant to primary co-surfactant weight ratio, in terms of grease removal and lack of slippery feeling, is a ratio of from 2:1 to 1:1.

The cleaning amines for use herein provide very good grease removal from dishware and the dishware does not feel slippery during rinse.

By "cleaning amine" is herein meant a molecule, having one of the formulas depicted herein below, comprising amine functionalities that helps cleaning as part of a cleaning composition. The term "cleaning amine" herein encompasses a single cleaning amine and a mixture thereof. The amine can be subjected to protonation depending on the pH of the cleaning medium in which it is used. The use of quatemized amines is envisaged in the present invention although it is not preferred.

Amines sometimes are used as solvents in detergent compositions. In the present invention the amines play an active role in the cleaning of greasy soils.

Cleaning amines for use herein include polyetheramines selected from the group consisting of polyetheramines of Formula (I), Formula (II), Formula (III) and a mixture thereof:

Formula (I)

Formula (II)

wherein each of R1-R12 is independently selected from H, alkyl, cycloalkyl, aryl, alkylaryl, or arylalkyl, wherein at least one of Ri-R ₆ and at least one of R7-R12 is different from H, each of A1-A9 is independently selected from linear or branched alkylenes having 2 to 18 carbon atoms, each of Z1-Z4 is independently selected from OH or NH2, wherein at least one of Z1-Z2 and at least one of Z3-Z4 is Ν¾, wherein the sum of x+y is in the range of about 2 to about 200, wherein x>l and y>l _i and the sum of xi + yi is in the range of about 2 to about 200, wherein x^l and yi≥l.

Formula (III)

wherein

R is selected from H or a C1-C6 alkyl group, each of ki, k2, and k3 is independently selected from 0, 1, 2, 3, 4, 5, or 6, each of A _l5 A ₂ , A3, A ₄ , A ₅ , and A ₆ is independently selected from a linear or branched alkylene group having from about 2 to about 18 carbon atoms or mixtures thereof, x >1, y >1, and z >1, and the sum of x+y+z is in the range of from about 3 to about 100, each of Zi, Z ₂ , and Z3 is independently selected from Ν¾ or OH, where at least two of Zi, Z ₂ , and Z3 are NH2 _; and the polyetheramine has a weight average molecular weight of from about 150 to about 1000 grams/mole.

Other preferred amines for use herein are amines of Formula (1):

wherein: Ri, R2, R _3, R ₄ , and R5 are independently selected from -H, linear, branched or cyclic alkyl or alkenyl having from 1 to 10 carbon atoms and n=0-3.

or Formula (2):

wherein and R ₄ are independently selected from -H, linear, branched or cyclic alkyl or alkenyl; and R ₂ is a linear, branched or cyclic alkyl or alkenyl having from 3 to 10 carbons, R3 is a linear or branched alkyl from 3 to 6 carbon atoms, R5 is H, methyl or ethyl and n=0-3.

The anionic surfactant can be any anionic cleaning surfactant, preferably the anionic surfactant comprises a sulphate anionic surfactant, more preferably an alkyl sulphate and/or alkoxylated sulfate anionic surfactant, preferably an alkyl alkoxylated anionic surfactant having an average alkoxylation degree of from about 0.2 to about 3, preferably from about 0.2 to about 2, most preferably from about 0.2 to about 1.0. Also preferred are branched anionic surfactants having a weight average level of branching of from about 5% to about 40%, more preferably alkyl alkoxylated anionic surfactants having a weight average level of branching of from about 5% to about 40%. Especially preferred anionic surfactant for use herein is an alkyl alkoxylated anionic surfactant having an average alkoxylation degree of from about 0.2 to about 1 and a weight average level of branching of from about 5% to about 40%. Preferably the composition of the invention comprises from about 10% to about 40%, preferably from about 15% to about 35%, more preferably from about 18% to about 32% by weight of the composition of the surfactant system. Preferably the composition of the invention comprises from about 5% to about 30% by weight of the composition of anionic surfactant, more preferably from about 8% to about 25%, yet more preferably from about 10% to about 20%.

Preferably the primary co-surfactant comprises amine oxide, more preferably the primary co- surfactant comprises at least 60% of amine oxide surfactant by weight of the primary co- surfactant. Preferably the primary co-surfactant comprises more than 80%, more preferably more than 99% by weight of the primary co-surfactant of amine oxide. Preferred amine oxide surfactant for use herein is an alkyl dimethyl amine oxide.

Preferably, the composition of the invention comprises a secondary co-surfactant. Preferably the anionic surfactant and the secondary co-surfactant are present in the composition of the invention in a weight ratio of from about 2.2: 1 to about 3.5: 1.

Especially preferred compositions from a grease cleaning and good rinse feel comprise anionic surfactant, primary and secondary co-surfactants in a weight ratio of from about 1 : 1:0.25 to 2:1 :0.7.

Preferably, the composition of the invention comprises a hydrotrope, more preferably sodium cumene sulfonate. The hydrotrope helps with the rheology profile of the composition. In particular it helps to thin the composition upon dilution that can contribute to faster release of cleaning actives and faster cleaning. This can be more important when the composition is used in manual dishwashing and the manual dishwashing takes place by delivering the composition onto a cleaning implement rather than delivering the composition onto a sink full of water.

According to another aspect of the invention there is provided a method of manual dishwashing using the composition of the invention.

There is also provided the use of the composition of the invention to provide grease cleaning and good feel during rinse. The elements of the composition of the invention described in connection with the first aspect of the invention apply mutatis mutandis to the other aspects of the invention.

DETAILED DESCRIPTION OF THE INVENTION

As used herein "liquid detergent composition" refers to those compositions that are employed in a variety of cleaning uses including dishes, or hard surfaces (e.g., floors, countertops etc), laundry, hair (e.g., shampoos), body, and the like. A preferred liquid detergent composition of the present invention is a "liquid dish detergent composition," which refers to those compositions that are employed in manual (i.e. hand) dish washing. Such compositions are generally high sudsing or foaming in nature. By "dish," the term include dishes, glasses, pots, pans, baking dishes, flatware and the like, made from ceramic, china, metal, glass, plastic (polyethylene, polypropylene, polystyrene, etc.), wood and the like. The composition of the invention is particularly good for the removal of grease from dishware, including plastic items. Surfactant System

The surfactant system of the composition of the invention comprises an anionic surfactant, a primary co-surfactant and optionally but preferably a secondary co- surfactant. The liquid detergent composition comprises from about 10% to about 40%, preferably from about 15% to about 35%, more preferably from about 18% to about 32% by weight of the composition of the surfactant system.

Anionic Surfactant The composition of the invention preferably comprises from 5% to 30%, more preferably 8% to 25% and especially from 10% to 20% of anionic surfactant by weight of the composition.

The anionic surfactant can be a single surfactant but usually it is a mixture of anionic surfactants. Preferably the anionic surfactant comprises a sulfate surfactant, more preferably a sulfate surfactant selected from the group consisting of alkyl sulfate, alkyl alkoxy sulfate and mixtures thereof. Preferred alkyl alkoxy sulfates for use herein are alkyl ethoxy sulfates.

The alkyl sulphate surfactant of the present invention preferably have the formula: RiO(A) _x S0 ₃ M, wherein the variables are herein defined. "Ri" is a Ci - C ₂ i alkyl or alkenyl group, preferably from C8-C2 ₀ , more preferably from C1 ₀ - Ci ₈ . The alkyl or alkenyl group may be branched or linear. Where the alkyl or alkenyl group is branched, it preferably comprises C1-4 alkyl branching units. The average weight percentage branching of the alkyl sulphate surfactant is preferably greater than 10%, more preferably from 15% to 80%, and most preferably from 20% to 40%, alternatively from 21% to 28%, alternatively combinations thereof. The branched alkyl sulphate surfactant can be a single alkyl sulphate surfactant or a mixture of alkyl sulphate surfactants. In the case of a single surfactant, the percentage of branching refers to the weight percentage of the hydrocarbyl chains that are branched in the original alcohol from which the surfactant is derived. In the case of a surfactant mixture, the percentage of branching is the weight average and it is defined according to the following formula: Weight average of branching (%) = [(xl * wt% branched alcohol 1 in alcohol 1 + x2 * wt% branched alcohol 2 in alcohol 2 + ....) / (xl + x2 + ....)] * 100; wherein xl, x2, are the weight in grams of each alcohol in the total alcohol mixture of the alcohols which were used as starting material for the anionic surfactant. In the weight average branching degree calculation the weight of alkyl sulphate surfactant components not having branched groups should also be included.

Turning back to the above formula, "A" is an alkoxy group, preferably a Ci - C5 alkoxy group, more preferably a Ci - C3 alkoxy group, yet more preferably the alkoxy group is selected from ethoxy, propoxy, and mixtures thereof. In one embodiment, the alkoxy group is ethoxy. "x" represents a mole percentage average below 1, preferably from 0 to below 1, more preferably from 0.1 to 0.9, alternatively from 0.2 to 0.8, alternatively combinations thereof.

For purposes of clarification, the formula above describes certain alkyl alkoxy sulfates; more preferably the formula describes a mixture of alkyl sulfates and alkyl alkoxy sulfates such that the alkoxylation on mole percentage average (i.e., variable "x") is below 1. In the case of a surfactant mixture, the average degree of alkoxylation is the mole percent average and it is defined according to the following formula: Mole average degree of alkoxylation = [(y0 * 0 + yl * 1 + y2 * 2 +....) / (y0 + yl + y2 + ....)]; wherein yO, yl, y2, ... are the mole percent of each sulphated surfactant in the total alkyl mixture of sulphated surfactants having respectively 0, 1, 2, alkoxy units which are present in the detergent of the invention. For example, an alkyl sulphate of the following formula CH ₃ (CH ₂ )i3S04 Na will have a y value of 0 (i.e., yO). An alkylethoxysulfate of the following formula CH ₃ (CH ₂ ) i3(OCH ₂ CH ₂ )S0 ₄ Na will have a y value of 1 (i.e., yl). An alkylethoxysulfate of the following formula: Na will have an y value of 4 (i.e., y4). The mole amount of each the three molecules is taken into account to ultimately calculate the mole percentage average of variable "x" (in the formula R _! 0(A) _x S0 ₃ M).

Regarding the formula RiO(A) _x S0 ₃ M, "M" is a cation, preferably the cation is selected from an alkali metal, alkali earth metal, ammonium group, or alkanolammonium group; more preferably the cation is sodium.

The detergent composition can optionally further comprise other anionic surfactants. Non- limiting examples include sulphonate, carboxylate, sulfosuccinate and sulfoacetate anionic surfactants. Primary co- surfactant

The composition of the invention comprises a primary co-surfactant. The composition preferably comprises from 3% to 25%, more preferably from 4% to 20% and especially from 5% to 15% by weight of the composition. The primary co-surfactant is selected from the group consisting of an amphoteric surfactant, a zwitterionic surfactant, and mixtures thereof. The composition of the present invention will preferably comprise an amine oxide as the amphoteric surfactant or betaine as the zwitterionic surfactant, or a mixture of said amine oxide and betaine surfactants.

Preferably the primary co-surfactant comprises an amphoteric surfactant. The amphoteric surfactant preferably comprises at least 40%, more preferably at least 50%, more preferably at least 60% and especially at least 80% by weight of an amine oxide surfactant. Alternatively the primary co-surfactant comprises an amphoteric and a zwitterionic surfactant, preferably the amphoteric and the zwitterionic surfactant are in a weight ratio of from about 2:1 to about 1:2, more preferably the amphoteric surfactant is an amine oxide surfactant and the zwitteronic surfactant is a betaine. Most preferably the co-surfactant is an amine oxide, especially alkyl dimethyl amine oxide. Most preferred among the amphoteric surfactants are amine oxides, especially coco dimethyl amine oxide or coco amido propyl dimethyl amine oxide. Amine oxide may have a linear or mid- branched alkyl moiety. Typical linear amine oxides include water-soluble amine oxides containing one Rl C _8- i ₈ alkyl moiety and 2 R2 and R3 moieties selected from the group consisting of C ₁ -3 alkyl groups and C ₁ -3 hydroxyalkyl groups. Preferably amine oxide is characterized by the formula Rl - N(R2)(R3) O wherein Ri is a C _8- i ₈ alkyl and R ₂ and R3 are selected from the group consisting of methyl, ethyl, propyl, isopropyl, 2-hydroxethyl, 2- hydroxypropyl and 3-hydroxypropyl. The linear amine oxide surfactants in particular may include linear Cio-Ci ₈ alkyl dimethyl amine oxides and linear C ₈ -Ci ₂ alkoxy ethyl dihydroxy ethyl amine oxides. Preferred amine oxides include linear C ₁₀ , linear C ₁₀ -C ₁₂ , and linear Ci ₂ -Ci ₄ alkyl dimethyl amine oxides.

Most preferred among the zwitterionic surfactants are betaines, such as alkyl betaines, alkylamidobetaine, amidazoliniumbetaine, sulfobetaine (INCI Sultaines) as well as the Phosphobetaine and preferably meets formula I: R'-fCO-X (CH ₂ ) _n ] _x -N ⁺ (R ² )(R ₃ )-(CH ₂ ) _m -[CH(OH)-CH ₂ ] _y -Y- (I) wherein

R ¹ is a saturated or unsaturated C6-22 alkyl residue, preferably C8-18 alkyl residue, in particular a saturated ClO-16 alkyl residue, for example a saturated C12-14 alkyl residue;

X is NH, NR ⁴ with CI -4 Alkyl residue R ⁴ , O or S,

n is a number from 1 to 10, preferably 2 to 5, in particular 3,

x is 0 or 1, preferably 1,

R ² , R ³ are independently a CI -4 alkyl residue, potentially hydroxy substituted such as a hydroxyethyl, preferably a methyl.

m is a number from 1 to 4, in particular 1, 2 or 3,

y is 0 or 1 and

Y is COO, S03, OPO(OR5)0 or P(0)(OR5)0, whereby R5 is a hydrogen atom H or a Cl- 4 alkyl residue.

Preferred betaines are the alkyl betaines of the formula (la), the alkyl amido betaine of the formula (lb), the Sulfo betaines of the formula (Ic) and the Amido sulfobetaine of the formula

(id);

R ¹ -N ⁺ (CH ₃ ) ₂ -CH ₂ COO ^" (la)

R ¹ -CO-NH(CH ₂ ) ₃ -N ⁺ (CH ₃ ) ₂ -CH ₂ COO ^" (lb)

R ¹ -N ⁺ (CH ₃ ) ₂ -CH ₂ CH(OH)CH ₂ S0 ₃ - (Ic)

R ¹ -CO-NH-(CH ₂ ) ₃ -N ⁺ (CH ₃ ) ₂ -CH ₂ CH(OH)CH ₂ S0 ₃ - (Id) in which R ¹ ! as the same meaning as in formula I. Particularly preferred betaines are the Carbobetaine [wherein Y ^" =COO ^~ ], in particular the Carbobetaine of the formula (la) and (lb), more preferred are the Alkylamidobetaine of the formula (lb). Examples of suitable betaines and sulfobetaine are the following [designated in accordance with INCI]: Almondamidopropyl of betaines, Apricotam idopropyl betaines, Avocadamidopropyl of betaines, Babassuamidopropyl of betaines, Behenam idopropyl betaines, Behenyl of betaines, betaines, Canolam idopropyl betaines, Capryl/Capram idopropyl betaines, Carnitine, Cetyl of betaines, Cocamidoethyl of betaines, Cocam idopropyl betaines, Cocam idopropyl Hydroxysultaine, Coco betaines, Coco Hydroxysultaine, Coco/Oleam idopropyl betaines, Coco Sultaine, Decyl of betaines, Dihydroxyethyl Oleyl Glycinate, Dihydroxyethyl Soy Glycinate, Dihydroxyethyl Stearyl Glycinate, Dihydroxyethyl Tallow Glycinate, Dimethicone Propyl of PG-betaines, Erucam idopropyl Hydroxysultaine, Hydrogenated Tallow of betaines, Isostearam idopropyl betaines, Lauram idopropyl betaines, Lauryl of betaines, Lauryl Hydroxysultaine, Lauryl Sultaine, Milkam idopropyl betaines, Minkamidopropyl of betaines, Myristam idopropyl betaines, Myristyl of betaines, Oleam idopropyl betaines, Oleam idopropyl Hydroxysultaine, Oleyl of betaines, Olivamidopropyl of betaines, Palmam idopropyl betaines, Palm itam idopropyl betaines, Palmitoyl Carnitine, Palm Kernelam idopropyl betaines, Polytetrafluoroethylene Acetoxypropyl of betaines, Ricinoleam idopropyl betaines, Sesam idopropyl betaines, Soyam idopropyl betaines, Stearam idopropyl betaines, Stearyl of betaines, Tallowam idopropyl betaines, Tallowam idopropyl Hydroxysultaine, Tallow of betaines, Tallow Dihydroxy ethyl of betaines, Undecylenam idopropyl betaines and Wheat Germam idopropyl betaines.

A preferred betaine is, for example, Cocoamidopropyl betaines (Cocoamidopropylbetain). Secondary co-surfactant

Preferably the composition of the invention comprises a non-ionic surfactant as secondary co- surfactant. Preferably from 0.1 to 10%, more preferably from 1% to 8%, especially from 3% to 6% of a nonionic surfactant by weight of the composition. Suitable nonionic surfactants include the condensation products of aliphatic alcohols with from 1 to 25 moles of alkylene oxide, preferably ethylene oxide. The alkyl chain of the aliphatic alcohol can either be straight or branched, primary or secondary, and generally contains from 8 to 22 carbon atoms. Particularly preferred are the condensation products of alcohols having an alkyl group containing from 8 to 18 carbon atoms, preferably from 10 to 15 carbon atoms, alternatively from 9 to 11 carbon atoms, alternatively from 12 to 14 carbon atoms, alternatively combinations thereof; with from 2 to 18 moles, preferably 2 to 15 moles, more preferably 5 tol2 molesof ethylene oxide per mole of alcohol. A preferred non-ionic surfactant includes an aliphatic alcohol with from 1 to 25 moles of ethylene oxide, preferably condensation products of alcohols having an alkyl group containing from 8 to 18 carbon atoms, with from 2 to 18 moles of ethylene oxide per mole of alcohol.

Also suitable are alkylpolyglycosides having the formula R ² 0(C _n H2 _n O) _t (glycosyl) _x (formula (III)), wherein R ² of formula (III) is selected from the group consisting of alkyl, alkyl-phenyl, hydroxyalkyl, hydroxyalkylphenyl, and mixtures thereof in which the alkyl groups contain from 10 to 18, preferably from 12 to 14, carbon atoms; n of formula (III) is 2 or 3, preferably 2; t of formula (III) is from 0 to 10, preferably 0; and x of formula (III) is from 1.3 to 10, preferably from 1.3 to 3, most preferably from 1.3 to 2.7. The glycosyl is preferably derived from glucose. Also suitable are alkylglycerol ethers and sorbitan esters. Also suitable are fatty acid amide surfactants having the formula (IV):

O

II

R ⁶ CN(R ⁷ ) ₂

(IV)

wherein R ⁶ of formula (IV) is an alkyl group containing from 7 to 21, preferably from 9 to 17, carbon atoms and each R ⁷ of formula (IV) is selected from the group consisting of hydrogen, Ci- C ₄ alkyl, Ci-C ₄ hydroxyalkyl, and -(C2H ₄ 0) _X H where x of formula (IV) varies from 1 to 3. Preferred amides are C8-C2 ₀ ammonia amides, monoethanolamides, diethanolamides, and isopropanolamides.

Most preferably the nonionic surfactant is a condensation product of an aliphatic alcohol with ethyleneoxide.

Preferably, the compositions of the present invention are free or substantially free of cationic surfactant.

Cleaning amine

The composition described herein includes from about 0.1% to about 10%, preferably, from about 0.2% to about 5%, and more preferably, from about 0.5% to about 4%, by weight of the composition, of a cleaning amine.

The term "cleaning amine" herein encompasses a single cleaning amine and a mixture thereof. A "cleaning amine" herein means a molecule comprising amine functionalities that helps cleaning as part of a cleaning composition.

The amine can be subjected to protonation depending on the pH of the cleaning medium in which it is used.

Cleaning amines for use herein include polyetheramines. One of the polyetheramine preferred for use in the composition of the invention is represented by the structure of Formula (I):

Formula (I) where each of Ri-R ₆ is independently selected from H, alkyl, cycloalkyl, aryl, alkylaryl, or arylalkyl, where at least one of Ri-R ₆ is different from H, typically at least one of Ri-R ₆ is an alkyl group having 2 to 8 carbon atoms, each of Ai-A ₆ is independently selected from linear or branched alkylenes having 2 to 18 carbon atoms, each of Zi-¾ is independently selected from OH or Ν¾, where at least one of Z1-Z2 is Ν¾, typically each of Zi and Z2 is NH2 _, where the sum of x+y is in the range of about 2 to about 200, typically about 2 to about 20, more typically about 2 to about 10 or about 3 to about 8 or about 4 to about 6, where x>l and y>l _i and the sum of xi + yi is in the range of about 2 to about 200, typically about 2 to about 20, more typically about 2 to about 10 or about 3 to about 8 or about 2 to about 4, where xi>l and y ₁ >l. Preferably in the polyetheramine of Formula (I), each of Ai-A ₆ is independently selected from ethylene, propylene, or butylene, typically each of Ai-A ₆ is propylene. More preferably, in the polyetheramine of Formula (I), each of Ri, R2, R5, and R ₆ is H and each of R ₃ and R ₄ is independently selected from C1-C16 alkyl or aryl, typically each of Ri, R2, R5, and R ₆ is H and each of R ₃ and R4 is independently selected from a butyl group, an ethyl group, a methyl group, a propyl group, or a phenyl group. More preferably, in the polyetheramine of Formula (I), R ₃ is an ethyl group, each of Ri, R2, R5, and R ₆ is H, and R ₄ is a butyl group. Especially, in the polyetheramine of Formula (I), each of Ri and R2 is H and each of R ₃ , R ₄ , R5, and R ₆ is independently selected from an ethyl group, a methyl group, a propyl group, a butyl group, a phenyl group, or H. In the polyetheramine represented by the structure of Formula (II):

Formula (II) each of R7-R12 is independently selected from H, alkyl, cycloalkyl, aryl, alkylaryl, or arylalkyl, where at least one of R7-R12 is different from H, typically at least one of R7-R12 is an alkyl group having 2 to 8 carbon atoms, each of A7-A9 is independently selected from linear or branched alkylenes having 2 to 18 carbon atoms, each of Z3-Z ₄ is independently selected from OH or Ν¾, where at least one of Z3-Z ₄ is Ν¾, typically each of Z3 and Z ₄ is NH2 _, where the sum of x+y is in the range of about 2 to about 200, typically about 2 to about 20, more typically about 2 to about 10 or about 3 to about 8 or about 2 to about 4, where x>l and y>l _i and the sum of i + yi is in the range of about 2 to about 200, typically about 2 to about 20, more typically about 2 to about 10 or about 3 to about 8 or about 2 to about 4, where xi>l and yi≥l.

Preferably in the polyetheramine of Formula (II), each of A ₇ -A ₉ is independently selected from ethylene, propylene, or butylene, typically each of A ₇ -Ag is propylene. More preferably, in the polyetheramine of Formula (II), each of R ₇ , Rg, Rn, and R12 is H and each of R9 and Rio is independently selected from C1-C16 alkyl or aryl, typically each of R ₇ , Rg, Rn, and R12 is H and each of R9 and Rio is independently selected from a butyl group, an ethyl group, a methyl group, a propyl group, or a phenyl group. More preferably, in the polyetheramine of Formula (II), R9 is an ethyl group, each of R ₇ , Rg, Rn, and R12 is H, and Rio is a butyl group. In some aspects, in the polyetheramine of Formula (II), each of R ₇ and Rg is H and each of R9, Rio, Rn, and R12 is independently selected from an ethyl group, a methyl group, a propyl group, a butyl group, a phenyl group, or H.

Preferred polyetheramines are selected from the group consisting of Formula A, Formula B, and mixtures thereof:

Formula A Formula B

Preferably, the polyetheramine comprises a mixture of the compound of Formula (I) and the compound of Formula (II).

Typically, the polyetheramine of Formula (I) or Formula (II) has a weight average molecular weight of less than about grams/mole 1000 grams/mole, preferably from about 100 to about 800 grams/mole, more preferably from about 200 to about 450 grams/mole.

The polyetheramine can comprise a polyetheramine mixture comprising at least 90%, by weight of the polyetheramine mixture, of the polyetheramine of Formula (I), the polyetheramine of Formula(II), the polyetheramine of Formula(III) or a mixture thereof. Preferably, the polyetheramine comprises a polyetheramine mixture comprising at least 95%, by weight of the polyetheramine mixture, of the polyetheramine of Formula (I), the polyetheramine of Formula(II) and the polyetheramine of Formula(III).

The polyetheramine of Formula (I) and/or the polyetheramine of Formula(II), are obtainable by: a) reacting a 1,3-diol of formula (1) with a C2-C1 ₈ alkylene oxide to form an alkoxylated 1,3-diol, wherein the molar ratio of 1,3-diol to C2-C1 ₈ alkylene oxide is in the range of about 1:2 to about

1:10,

(1)

where Ri-R ₆ are independently selected from H, alkyl, cycloalkyl, aryl, alkylaryl, or arylalkyl, where at least one of Ri-R ₆ is different from H;

b) animating the alkoxylated 1,3-diol with ammonia.

The molar ratio of 1,3-diol to C2-C1 ₈ alkylene oxide is preferably in the range of about 1:3 to aboutl:8, more typically in the range of about 1:4 to about 1:6. Preferably, the C2-C1 ₈ alkylene oxide is selected from ethylene oxide, propylene oxide, butylene oxide or a mixture thereof. More preferably, the C2-C1 ₈ alkylene oxide is propylene oxide.

In the 1,3-diol of formula (1), Ri, R2, R5, and R ₆ are H and R3 and R4 are C1- 16 alkyl or aryl. Preferably, the 1,3-diol of formula (1) is selected from 2-butyl-2-ethyl-l,3-propanediol, 2- methyl-2-propyl-l,3-propanediol, 2-methyl-2-phenyl-l,3-propanediol, 2,2-dimethyl-l,3- propandiol, 2-ethyl-l,3-hexandiol, or a mixture thereof.

Step a): Alkoxylation

The 1,3-diols of Formula (1) are synthesized as described in WO10026030, WO10026066, WO09138387, WO09153193, and WO10010075. Suitable 1,3-diols include 2,2-dimethyl-l,3- propane diol, 2-butyl-2-ethyl- 1,3-propane diol, 2-pentyl-2-propyl- 1,3-propane diol, 2-(2- methyl)butyl-2-propyl- 1,3-propane diol, 2,2,4-trimethyl- 1,3-propane diol, 2,2-diethyl-l,3- propane diol, 2-methyl-2-propyl-l,3-propane diol, 2-ethyl-l,3-hexane diol, 2-phenyl-2-methyl- 1,3-propane diol, 2-methyl- 1,3-propane diol, 2-ethyl-2-methyl-l,3 propane diol, 2,2-dibutyl-l,3- propane diol, 2,2-di(2-methylpropyl)- 1,3-propane diol, 2-isopropyl-2-methyl- 1,3-propane diol, or a mixture thereof. In some aspects, the 1,3-diol is selected from 2-butyl-2-ethyl-l,3- propanediol, 2-methyl-2-propyl-l,3-propanediol, 2-methyl-2-phenyl-l,3-propanediol, or a mixture thereof. Typically used 1,3-diols are 2-butyl-2-ethyl-l,3-propanediol, 2-methyl-2- propyl-l,3-propanediol, 2-methyl-2-phenyl-l,3-propanediol. An alkoxylated 1,3-diol may be obtained by reacting a 1,3-diol of Formula I with an alkylene oxide, according to any number of general alkoxylation procedures known in the art. Suitable alkylene oxides include C2-C1 ₈ alkylene oxides, such as ethylene oxide, propylene oxide, butylene oxide, pentene oxide, hexene oxide, decene oxide, dodecene oxide, or a mixture thereof. In some aspects, the C2-C1 ₈ alkylene oxide is selected from ethylene oxide, propylene oxide, butylene oxide, or a mixture thereof. A 1,3-diol may be reacted with a single alkylene oxide or combinations of two or more different alkylene oxides. When using two or more different alkylene oxides, the resulting polymer may be obtained as a block-wise structure or a random structure.

Typically, the molar ratio of 1,3- diol to C2-C1 ₈ alkylene oxide at which the alkoxylation reaction is carried out is in the range of about 1:2 to about 1:10, more typically about 1:3 to about 1:8, even more typically about 1:4 to about 1:6.

The alkoxylation reaction generally proceeds in the presence of a catalyst in an aqueous solution at a reaction temperature of from about 70°C to about 200°C and typically from about 80°C to about 160°C. The reaction may proceed at a pressure of up to about 10 bar or up to about 8 bar. Examples of suitable catalysts include basic catalysts, such as alkali metal and alkaline earth metal hydroxides, e.g., sodium hydroxide, potassium hydroxide and calcium hydroxide, alkali metal alkoxides, in particular sodium and potassium Ci-C4-alkoxides, e.g., sodium methoxide, sodium ethoxide and potassium tert-butoxide, alkali metal and alkaline earth metal hydrides, such as sodium hydride and calcium hydride, and alkali metal carbonates, such as sodium carbonate and potassium carbonate. In some aspects, the catalyst is an alkali metal hydroxides, typically potassium hydroxide or sodium hydroxide. Typical use amounts for the catalyst are from about 0.05 to about 10% by weight, in particular from about 0.1 to about 2% by weight, based on the total amount of 1,3-diol and alkylene oxide.

Alkoxylation with x+y C2-C1 ₈ alkylene oxides and/or xi+yi C2-C1 ₈ alkylene oxides produces structures as represented by Formula 2 and/or Formula 3 :

Formula (2)

Formula (3) where R1-R12 are independently selected from H, alkyl, cycloalkyl, aryl, alkylaryl, or arylalkyl, where at least one of Ri-R ₆ and at least one of R7-R12 is different from H, each of A1-A9 is independently selected from linear or branched alkylenes having 2 to 18 carbon atoms, typically 2-10 carbon atoms, more typically 2-5 carbon atoms, and the sum of x+y is in the range of about 2 to about 200, typically about 2 to about 20, more typically about 2 to about 10 or about 2 to about 5, where x>l and y>l _i and the sum of xi + yi is in the range of about 2 to about 200, typically about 2 to about 20, more typically about 2 to about 10 or about 2 to about 5, where X _! >1 and yi≥l.

Step b): Amination

Amination of the alkoxylated 1,3-diols produces structures represented by Formula I or Formula

Formula (II)

where each of R1-R12 is independently selected from H, alkyl, cycloalkyl, aryl, alkylaryl, or arylalkyl, where at least one of Ri-R ₆ and at least one of R7-R12 is different from H, each of A1-A9 is independently selected from linear or branched alkylenes having 2 to 18 carbon atoms, typically 2-10 carbon atoms, more typically, 2-5 carbon atoms, each of Z1-Z4 is independently selected from OH or NH ₂ , where at least one of Zi-Z ₂ and at least one of Z3-Z4 is NH ₂ , where the sum of x+y is in the range of about 2 to about 200, typically about 2 to about 20, more typically about 2 to about 10 or about 2 to about 5, where x>l and y>l _i and the sum of xi + yi is in the range of about 2 to about 200, typically about 2 to about 20, more typically about 2 to about 10 or about 2 to about 5, where xi>l and yi>l.

Polyetheramines according to Formula I and/or Formula II are obtained by reductive amination of the alkoxylated 1,3-diol mixture (Formula 2 and Formula 3) with ammonia in the presence of hydrogen and a catalyst containing nickel. Suitable catalysts are described in WO

2011/067199A1, WO2011/067200A1, and EP0696572 Bl. Preferred catalysts are supported copper-, nickel-, and cobalt-containing catalysts, where the catalytically active material of the catalyst, before the reduction thereof with hydrogen, comprises oxygen compounds of aluminum, copper, nickel, and cobalt, and, in the range of from about 0.2 to about 5.0% by weight of oxygen compounds, of tin, calculated as SnO. Other suitable catalysts are supported copper-, nickel-, and cobalt-containing catalysts, where the catalytically active material of the catalyst, before the reduction thereof with hydrogen, comprises oxygen compounds of aluminum, copper, nickel, cobalt and tin, and, in the range of from about 0.2 to about 5.0% by weight of oxygen compounds, of yttrium, lanthanum, cerium and/or hafnium, each calculated as Y2O ₃ , La ₂ 0 ₃ , Ce ₂ 0 ₃ and Hf ₂ 0 _3, respectively. Another suitable catalyst is a zirconium, copper, and nickel catalyst, where the catalytically active composition comprises from about 20 to about 85 % by weight of oxygen-containing zirconium compounds, calculated as Zr0 ₂ , from about 1 to about 30% by weight of oxygen-containing compounds of copper, calculated as CuO, from about 30 to about 70 % by weight of oxygen-containing compounds of nickel, calculated as NiO, from about 0.1 to about 5 % by weight of oxygen-containing compounds of aluminium and/ or manganese, calculated as AI2O ₃ and Mn0 ₂ respectively.

For the reductive amination step, a supported as well as non-supported catalyst may be used. The supported catalyst is obtained, for example, by deposition of the metallic components of the catalyst compositions onto support materials known to those skilled in the art, using techniques which are well-known in the art, including without limitation, known forms of alumina, silica, charcoal, carbon, graphite, clays, mordenites; and molecular sieves, to provide supported catalysts as well. When the catalyst is supported, the support particles of the catalyst may have any geometric shape, for example spheres, tablets, or cylinders, in a regular or irregular version. The process may be carried out in a continuous or discontinuous mode, e.g. in an autoclave, tube reactor, or fixed-bed reactor. The feed thereto may be upflowing or downflowing, and design features in the reactor which optimize plug flow in the reactor may be employed. The degree of amination is from about 50% to about 100%, typically from about 60% to about 100%, and more typically from about 70% to about 100%.

The degree of amination is calculated from the total amine value (AZ) divided by sum of the total acetylables value (AC) and tertiary amine value (tert. AZ) multiplied by 100: (Total AZ: (AC+tert. AZ))xl00). The total amine value (AZ) is determined according to DIN 16945. The total acetylables value (AC) is determined according to DIN 53240. The secondary and tertiary amines are determined according to ASTM D2074-07.

The hydroxyl value is calculated from (total acetylables value + tertiary amine value)- total amine value. The polyetheramines of the invention are effective for removal of greasy soils, in particular removal of crystalline grease. Especially preferred for use herein is a polyethylene amine of Formula (I) having the following structure formula:

wherein n+m is from 0 to 8. Preferably n+m is from 0 to 6 and more preferably from 1 to 6.

The polyetheramine may be a polyetheramine of Formula (III),

Formula (III)

wherein

R is selected from H or a C1-C6 alkyl group,

each of k _l5 k ₂ , and k ₃ is independently selected from 0, 1, 2, 3, 4, 5, or 6,

each of Ai, A ₂ , A3, A ₄ , A5, and A ₆ is independently selected from a linear or branched alkylene group having from about 2 to about 18 carbon atoms or mixtures thereof,

x >1, y >1, and z >1, and the sum of x+y+z is in the range of from about 3 to about 100, and each of Zi, Z ₂ , and Z3 is independently selected from NH ₂ or OH, where at least two of Zi, Z ₂ , and Z3 are NH ₂ .

Preferably, R is H or a C1-C6 alkyl group selected from methyl, ethyl, or propyl. In some aspects, R is H or a C1-C6 alkyl group selected from ethyl.

Preferably, each of ki, k ₂ , and k3 is independently selected from 0, 1, or 2. Each of ki, k ₂ , and k3 may be independently selected from 0 or 1. More preferably, at least two of ki, k ₂ , and k3 are 1 and even more preferably, each of ki, k ₂ , and k3 is 1.

Preferably, each of Zi, Z ₂ , and Z3 is NH ₂ .

All A groups (i.e., Ai-A ₆ ) may be the same, at least two A groups may be the same, at least two A groups may be different, or all A groups may be different from each other. Each of Ai, A ₂ , A3, A ₄ , A5, and A ₆ may be independently selected from a linear or branched alkylene group having from about 2 to about 10 carbon atoms, or from about 2 to about 6 carbon atoms, or from about 2 to about 4 carbon atoms, or mixtures thereof. Preferably, at least one, or at least three, of A _! -A ₆ is a linear or branched butylene group. More preferably, each of A ₄ , A ₅ , and A ₆ is a linear or branched butylene group. Especially, each of A _! -A ₆ is a linear or branched butylene group. Preferably, x, y, and/or z are independently selected and should be equal to 3 or greater, meaning that that the polyetheramine may have more than one [Ai - O] group, more than one [A ₂ - O] group, and/or more than one [A3 - O] group. Preferably, Ai is selected from ethylene, propylene, butylene, or mixtures thereof. Preferably, A ₂ is selected from ethylene, propylene, butylene, or mixtures thereof. Preferably, A3 is selected from ethylene, propylene, butylene, or mixtures thereof. When Ai, A ₂ , and/or A3 are mixtures of ethylene, propylene, and/or butylenes, the resulting alkoxylate may have a block-wise structure or a random structure.

[Ai - 0] _x -i can be selected from ethylene oxide, propylene oxide, butylene oxide, or mixtures thereof. [A ₂ - 0] _y _i can be selected from ethylene oxide, propylene oxide, butylene oxide, or mixtures thereof. [A3 - 0] _z _i can be selected from ethylene oxide, propylene oxide, butylene oxide, or mixtures thereof. Preferably, the sum of x+y+z is in the range of from about 3 to about 100, or from about 3 to about 30, or from about 3 to about 10, or from about 5 to about 10.

Typically, the polyetheramines of the present invention have a weight average molecular weight of from about 150, or from about 200, or from about 350, or from about 500 grams/mole, to about 1000, or to about 900, or to about 800 grams/mole.

Preferably, when the polyetheramine is a polyetheramine of Formula (III) where R is a C2 alkyl group (i.e., ethyl) and optionally each of ki, k2, and k ₃ is 1, the molecular weight of the polyetheramine is from about 500 to about 1000, or to about 900, or to about 800 grams/mole. It is also preferred, when the polyetheramine is a polyetheramine of Formula (III) where R is a C2 alkyl group (i.e., ethyl) and optionally each of ki, k2, and k ₃ is 1, at least one A group (i.e., at least one of Al, A2, A3, A4, A5, or A6) is not a propylene group. It is also preferred, when the polyetheramine is a polyetheramine of Formula (III) where R is a C2 alkyl group (i.e., ethyl) and optionally each of ki, k2, and k ₃ is 1, at least one A group (i.e., at least one of Al, A2, A3, A4, A5, or A6) is a ethylene group or a butylene group, or more typically at least one A group (i.e., at least one of Al, A2, A3, A4, A5, or A6) is a butylene group.

Polyetheramine with

Formula C where average n is from about 0.5 to about 5, or from about 1 to about 3, or from about 1 to about 2.5.

Other preferred polyetheramines are selected from the group consisting of Formula C, Formula D, Formula E, and mixtures thereof:

Formula D Formula E

Formula C

where average n is from about 0.5 to about 5.

The polyetheramines of Formula (III) of the present invention may be obtained by a process comprising the following steps:

a) reacting a low-molecular-weight, organic triol, such as glycerine and/or 1,1,1- trimethylolpropane, with C2-C18 alkylene oxide, to form an alkoxylated triol, where the molar ratio of the low-molecular-weight organic triol to the alkylene oxide is in the range of about 1:3 to about 1: 10, and

b) aminating the alkoxylated triol with ammonia.

This process is described in more detail below. Alkoxylation

Polyetheramines according to Formula (III) may be obtained by reductive amination of an alkoxylated triol. Alkoxylated triols according to the present disclosure may be obtained by reaction of low-molecular-weight, organic triols, such as glycerine and/or 1,1,1- trimethylolpropane, with alkylene oxides according to general alkoxylation procedures known in the art.

By "low-molecular-weight," it is meant that the triol has a molecular weight of from about 64 to about 500, or from about 64 to about 300, or from about 78 to about 200, or from about 92 to about 135 g / mol. The triol may be water soluble.

A low-molecular-weight, organic triol useful herein (or simply "low-molecular-weight triol," as used herein) has the structure of Formula (4):

where R is selected from H or a C1-C6 alkyl group, and where each k is independently selected from 0, 1, 2, 3, 4, 5, or 6. Preferably, R is H or a C1-C6 alkyl group selected from methyl, ethyl, or propyl. More preferably, R is H or ethyl, ki, k2, and k ₃ can each be independently selected from 0, 1, or 2. Each of ki, k2, and k ₃ may be independently selected from 0 or 1. Preferably, at least two of ki, k2, and k ₃ are 1. More preferably, all three of ki, k2, and k ₃ are 1.

The low-molecular-weight triol can be selected from glycerine, 1,1,1-trimethylolpropane, or mixtures thereof.

glycerine 1,1,1 -trimethylolpropane

The alkoxylated triol, such as alkoxylated glycerine or alkoxylated 1,1,1-trimethylolpropane, may be prepared in a known manner by reaction of the low-molecular-weight triol with an alkylene oxide. Suitable alkylene oxides are linear or branched C2-C1 ₈ alkylene oxides, typically C2-C1 ₀ alkylene oxides, more typically C2-C6 alkylene oxides or C2-C4 alkylene oxides. Suitable alkylene oxides include ethylene oxide, propylene oxide, butylene oxide, pentene oxide, hexene oxide, decene oxide, and dodecene oxide. In some aspects, the C2-C1 ₈ alkylene oxide is selected from ethylene oxide, propylene oxide, butylene oxide, or a mixture thereof. In some aspects, the C2-C1 ₈ alkylene oxide is butylene oxide, optionally in combination with other C2-C1 ₈ alkylene oxides.

The low molecular weight triols, such as glycerine or 1,1,1-trimethylolpropane, may be reacted with one single type of alkylene oxide or combinations of two or more different types of alkylene oxides, e.g., ethylene oxide and propylene oxide. If two or more different types of alkylene oxides are used, the resulting alkoxylate may have a block- wise structure or a random structure.

Typically, the molar ratio of low-molecular-weight triol to C2-C1 ₈ alkylene oxide at which the alkoxylation reaction is carried out is in the range of about 1:3 to about 1:10, more typically about 1:3 to about 1:6, even more typically about 1:4 to about 1:6. In some aspects, the molar ratio of low-molecular-weight triol to C2-C1 ₈ alkylene oxide at which the alkoxylation reaction is carried out is in the range of about 1:5 to about 1: 10. When the low-molecular- weight triol is 1,1,1-trimethylolpropane, or when R of the triol of Formula (2) is a C2 alkyl and each of ki, k2, and k ₃ are 1, the polyetheramine has a weight average molecular weight of from about 500 to about 1000, or to about 900, or to about 800 grams/mole.

The reaction is generally performed in the presence of a catalyst in an aqueous solution at a reaction temperature of from about 70°C to about 200°C, and typically from about 80°C to about 160°C. This reaction may be performed at a pressure of up to about 10 bar, or up to about 8 bar. Examples of suitable catalysts are basic catalysts such as alkali metal and alkaline earth metal hydroxides, such as sodium hydroxide, potassium hydroxide and calcium hydroxide, alkali metal alkoxides, in particular sodium and potassium Ci-C4-alkoxides, such as sodium methoxide, sodium ethoxide and potassium tert-butoxide, alkali metal and alkaline earth metal hydrides, such as sodium hydride and calcium hydride, and alkali metal carbonates, such as sodium carbonate and potassium carbonate. Alkali metal hydroxides, such as potassium hydroxide and sodium hydroxide, are particularly suitable. Typical use amounts for the basic catalyst are from about 0.05 to about 10% by weight, in particular from about 0.1 to about 2% by weight, based on the total amount of the low-molecular-weight triol and the alkylene oxide.

Amination Polyetheramines according to Formula (III) may be obtained by reductive amination of an alkoxylated triol, such as those described above, for example alkoxylated glycerine or alkoxylated 1,1,1-trimethylolpropane, with ammonia in the presence of hydrogen and a catalyst, such as a catalyst containing nickel. Suitable catalysts are described in WO 2011/067199 Al, in WO2011/067200 Al, and in EP0696572 Bl.

The amination may be carried out in the presence of copper-, nickel- or cobalt-containing catalyst. Preferred catalysts are supported copper-, nickel- and cobalt-containing catalysts, wherein the catalytically active material of the catalysts, before the reduction thereof with hydrogen, comprises oxygen compounds of aluminium, copper, nickel and cobalt, and, in the range of from about 0.2% to about 5.0% by weight, of oxygen compounds of tin, calculated as SnO. Other preferred catalysts are supported copper-, nickel- and cobalt-containing catalysts, wherein the catalytically active material of the catalysts, before the reduction thereof with hydrogen, comprises oxygen compounds of aluminium, copper, nickel, cobalt, tin, and, in the range of from about 0.2 to about 5.0% by weight, of oxygen compounds of yttrium, lanthanum, cerium and/or hafnium, each calculated as Y2O ₃ , La ₂ 0 ₃ , Ce ₂ 0 ₃ and Hf ₂ 0 ₃ , respectively. Another suitable catalyst is a zirconium, copper, nickel catalyst, wherein the catalytically active composition comprises from about 20 to about 85 % by weight of oxygen-containing zirconium compounds, calculated as Zr0 ₂ , from about 1 to about 30% by weight of oxygen-containing compounds of copper, calculated as CuO, from about 30 to about 70 % by weight of oxygen- containing compounds of nickel, calculated as NiO, from about 0.1 to about 5 % by weight of oxygen-containing compounds of aluminium and/ or manganese, calculated as AI2O ₃ and Mn02, respectively.

For the reductive amination step, a supported as well as a non-supported catalyst can be used. The supported catalyst may be obtained by deposition of the metallic components of the catalyst compositions onto support materials known to those skilled in the art, using techniques that are well-known in the art, including, without limitation, known forms of alumina, silica, charcoal, carbon, graphite, clays, mordenites; molecular sieves may be used to provide supported catalysts as well. When the catalyst is supported, the support particles of the catalyst may have any geometric shape, for example, the shape of spheres, tablets, or cylinders in a regular or irregular version.

The process can be carried out in a continuous or discontinuous mode, e.g., in an autoclave, tube reactor, or fixed-bed reactor. A number of reactor designs may be used. For example, the feed thereto may be upflowing or downflowing, and design features in the reactor that optimize plug flow in the reactor may be employed.

The degree of amination may be from about 67% to about 100%, or from about 85% to about

100%. The degree of amination is calculated from the total amine value (AZ) divided by sum of the total acetylables value (AC) and tertiary amine value (tert. AZ) multiplied by 100 (Total AZ / ((AC+tert. AZ)xl00)).

The total amine value (AZ) is determined according to DIN 16945.

The total acetylables value (AC) is determined according to DIN 53240.

The secondary and tertiary amines are determined according to ASTM D2074-07.

The hydroxyl value is calculated from (total acetylables value + tertiary amine value) - total amine value. Amine of Formula ( 1 ) :

The cleaning amine of Formula (1) has an ethylene diamine core with at least one primary amine functionality. The cleaning amine also comprises at least another nitrogen atom, preferable in the form of a tertiary amine functionality. Herein the term "core" refers to the alkyl chain between two nitrogen radicals. The number of carbons in the core does not include the radicals attached to the core.

The cle

wherein: Ri, R2, R3, R4, and R5 are independently selected from -H, linear, branched or cyclic alkyl or alkenyl having from 1 to 10 carbon atoms and n=0-3.

Preferably, the cleaning amine is aliphatic in nature. The cleaning amine preferably has a molecular weight of less than about 1000 grams/mole and more preferably less than about 450 grams/mole.

"n" varies from 0 to not more than 3, preferably "n" is 0. The amine molecule contains at least one primary amine functionality and preferably a tertiary amine functionality.

Suitable cleaning amines for use herein include amines wherein Ri and R2 are selected from isopropyl and butyl, preferably Ri and R2 are both isopropyl or both butyl.

Preferably cleaning amines include those in which RI and R2 are isopropyl and preferably, n is 0. Also h RI and R2 are butyl and preferably, n is 0

N 5 _s N diiso ro yfet ane~1 ,2-cf iarrmie R5 is preferably -CH3 or -CH2CH3. Cleaning amines in which R5 is -CH3 or -CH2CH3 could be good in terms of composition stability. Without being bound by theory, it is believed that the methyl or ethyl radical can provide stearic hinderance that protects the cleaning amine from negative interaction with other components of the cleaning composition.

Amine

wherein Ri and R4 are independently selected from -H, linear, branched or cyclic alkyl or alkenyl ; having from 1 to 10 carbon atoms and R2 is a linear, branched or cyclic alkyl or alkenyl having from 3 to 10 carbons, R3 is a linear or branched alkyl from 3 to 6 carbon atoms, R5 is H, methyl or ethyl and is preferably located in alpha position from the amine functionality/ies, and n=0-3.

The cleaning amine of formula (2) has a C3-C6 diamine core with at least one of the amine functionalities being a primary amine. Herein the term "core" refers to the alkyl chain between two nitrogen radicals. The number of carbons in the core does not include the radicals attached to the core.

The cleaning amine of formula (2) preferably has a molecular weight of less than about 1000 grams/mole and more preferably less than about 450 grams/mole.

"n" varies from 0 to not more than 3, preferably "n" is 0. The amine molecule contains at least one primary amine functionality and preferably a tertiary amine functionality.

Suitable cleaning amines include amines wherein Ri and R2 are selected from propyl, butyl and

2 are both propyl, butyl or hexyl. Preferably n is 0.

N'N'-dipropylpropane 1,3 ldiamine

. ^iiHit iKOpane-l ,3- iamine

Another preferred cleaning amine for use herein is cyclohexyl propylenediamine (wherein n=0, Rl is c clohexanyl and R2 is H)

Especially preferred for use herein is the amine of Formula (3) Water The liquid detergent compositions preferably comprise water. The water may be added to the composition directly or may be brought into the composition with raw materials. In any event, the total water content of the composition herein may comprise from 10% to 95% water by weight of the liquid dish detergent compositions. Alternatively, the composition may comprise from 20% to 95%, alternatively from 30% to 90%, or from 40% to 85% alternatively combinations thereof, of water by weight of the liquid dish detergent composition.

Organic Solvents The present compositions may optionally comprise an organic solvent. For the purpose of this invention "organic solvent" excludes cleaning amines. Suitable organic solvents include C _4- i ₄ ethers and diethers, polyols, glycols, alkoxylated glycols, C ₆ -Ci ₆ glycol ethers, alkoxylated aromatic alcohols, aromatic alcohols, aliphatic linear or branched alcohols, alkoxylated aliphatic linear or branched alcohols, alkoxylated C1-C5 alcohols, C ₈ -Ci ₄ alkyl and cycloalkyl hydrocarbons and halohydrocarbons, and mixtures thereof. Preferably the organic solvents include alcohols, glycols, and glycol ethers, alternatively alcohols and glycols. In one embodiment, the liquid detergent composition comprises from 0% to less than 50% of a solvent by weight of the composition. When present, the liquid detergent composition will contain from 0.01% to 20%, alternatively from 0.5% to 15%, alternatively from 1% to 10% by weight of the liquid detergent composition of said organic solvent. Non-limiting examples of specific solvents include propylene glycol, polypropylene glycol, propylene glycol phenyl ether, ethanol, and combinations thereof. In one embodiment, the composition comprises from 0.01% to 20% of an organic solvent by weight of the composition, wherein the organic solvent is selected from glycols, polyalkyleneglycols, glycol ethers, ethanol, and mixtures thereof.

Hydrotrope

The liquid detergent compositions optionally comprises a hydrotrope in an effective amount, i.e. from 0 % to 15%, or from 0.5 % to 10 % , or from 1 % to 6 %, or from 0.1% to 3%, or combinations thereof, so that the liquid dish detergent compositions are compatible or more compatible in water. Suitable hydrotropes for use herein include anionic-type hydrotropes, particularly sodium, potassium, and ammonium xylene sulfonate, sodium, potassium and ammonium toluene sulfonate, sodium potassium and ammonium cumene sulfonate, and mixtures thereof, as disclosed in U.S. Patent 3,915,903. In one embodiment, the composition of the present invention is isotropic. An isotropic composition is distinguished from oil-in-water emulsions and lamellar phase compositions. Polarized light microscopy can assess whether the composition is isotropic. See e.g., The Aqueous Phase Behaviour of Surfactants, Robert Laughlin, Academic Press, 1994, pp. 538-542. In one embodiment, an isotropic dish detergent composition is provided. In one embodiment, the composition comprises 0.1% to 3% of a hydrotrope by weight of the composition, preferably wherein the hydrotrope is selected from sodium, potassium, and ammonium xylene sulfonate, sodium, potassium and ammonium toluene sulfonate, sodium potassium and ammonium cumene sulfonate, and mixtures thereof. Calcium / Magnesium ions

Calcium ion and/or Magnesium ion, preferably Magnesium ion, are added, preferably as a hydroxide, chloride, acetate, sulphate, formate, oxide or nitrate salt, to the compositions of the present invention, typically at an active level of from 0.01% to 1.5%, preferably from 0.015% to 1%, more preferably from 0.025 % to 0.5%, by weight of the liquid detergent composition. In one embodiment, the composition comprises from 0.01% to 1.5% of a calcium ion or magnesium ion, or mixtures thereof, by weight of the composition, preferably the magnesium ion.

Adjunct Ingredients

The liquid detergent compositions herein can optionally further comprise a number of other adjunct ingredients suitable for use in liquid detergent compositions such as perfume, colorants, pearlescent agents, opacifiers, suds stabilizers / boosters, cleaning and/or shine polymers, rheology modifying polymers, structurants, chelants, skin care actives, suspended particles, enzymes, anti-caking agents, viscosity trimming agents (e.g. salt such as NaCl and other mono-, di- and trivalent salts), preservatives and pH trimming and/or buffering means (e.g. carboxylic acids such as citric acid, HC1, NaOH, KOH, alkanolamines, phosphoric and sulfonic acids, carbonates such as sodium carbonates, bicarbonates, sesquicarbonates, borates, silicates, phosphates, imidazole and alike). pH

The liquid detergent compositions herein preferably have a pH adjusted to between 6.5 and 12, more preferably between 7 and 11, more preferably between 7.5 and 10 and especially between 8.5 to 9.5. H is determined by the liquid detergent composition diluted with deionized water making a 10% product concentration by weight (i.e., 10% product and 90% water, by weight). The pH is measured at 20°C. The pH of the composition can be adjusted using pH trimming and/or buffering means known in the art.

Viscosity

The liquid detergent compositions of the present invention can be Newtonian or non-Newtonian with a viscosity of between 1 centipoises (cps) and 5,000cps at 20 °C and, alternatively between lOcps and 2,000cps, or between 50cps and l,500cps, or between lOOcps and l,000cps, alternatively combinations thereof.

Viscosity is measured with a BROOFIELD DV-E viscometer, at 20°C, spindle number 31. The following rotations per minute (rpm) should be used depending upon the viscosity: Between 300 cps to below 500 cps is at 50 rpm; between 500 cps to less than 1,000 cps is at 20 rpm; from 1,000 cps to less than 1,500 cps at 12 rpm; from 1,500 cps to less than 2,500 cps at 10 rpm; from 2,500 cps, and greater, at 5 rpm. Those viscosities below 300 cps are measured at 12 rpm with spindle number 18. Packaging

The liquid detergent compositions of the present invention may be packed in any suitable packaging for delivering the liquid detergent composition for use. In one preferred embodiment, the package may be comprised of polyethylene terephthalate, high-density polyethylene, low- density polyethylene, or combinations thereof. Furthermore, preferably, the package may be dosed through a cap at the top of the package such that the composition exits the bottle through an opening in the cap. The cap may be a push-pull cap or a flip top cap.

Method of the invention

The method of the invention comprises the steps of:

i) delivering a detergent composition in its neat form onto the dishware or a cleaning implement. By "neat form" is herein meant that the detergent composition is delivered onto the dishware or cleaning implement as it is, without previously diluting the composition with water. ii) cleaning the dishware with the detergent composition in the presence of water. The water can be present by putting the dishware under a running tap, wetting the cleaning implement, etc and iii) optionally rinsing the dishware. Alternative, the composition can be pre-dissolved in a sink of water to create a wash solution and the soiled dishware is immersed in the wash solution. The dishware can be subsequently rinsed.

Method of washing Other aspects of the invention are directed to methods of washing dishware with the composition of the present invention. Said methods comprise the step of applying the composition, preferably in liquid form, onto the dishware surface, either in diluted or neat form and rinsing or leaving the composition to dry on the surface without rinsing the surface. By "in its neat form", it is meant herein that said composition is applied directly onto the surface to be treated and/or onto a cleaning device or implement such as a dish cloth, a sponge or a dish brush without undergoing any dilution (immediately) prior to the application. The cleaning device or implement is preferably wet before or after the composition is delivered to it. By "diluted form", it is meant herein that said composition is diluted by the user with an appropriate solvent, typically water. By "rinsing", it is meant herein contacting the dishware cleaned using a process according to the present invention with substantial quantities of appropriate solvent, typically water, after the step of applying the liquid composition herein onto said dishware. By "substantial quantities", it is meant usually about 1 to about 10 liters. The composition herein can be applied in its diluted form. Soiled dishes are contacted with an effective amount, typically from about 0.5 ml to about 20 ml (per about 25 dishes being treated), preferably from about 3ml to about 10 ml, of the detergent composition, preferably in liquid form, of the present invention diluted in water. The actual amount of detergent composition used will be based on the judgment of user, and will typically depend upon factors such as the particular product formulation of the composition, including the concentration of active ingredients in the composition, the number of soiled dishes to be cleaned, the degree of soiling on the dishes, and the like. Generally, from about 0.01 ml to about 150 ml, preferably from about 3ml to about 40ml of a liquid detergent composition of the invention is combined with from about 2000 ml to about 20000 ml, more typically from about 5000 ml to about 15000 ml of water in a sink having a volumetric capacity in the range of from about 1000 ml to about 20000 ml, more typically from about 5000 ml to about 15000 ml. The soiled dishes are immersed in the sink containing the diluted compositions then obtained, where contacting the soiled surface of the dish with a cloth, sponge, or similar article cleans them. The cloth, sponge, or similar article may be immersed in the detergent composition and water mixture prior to being contacted with the dish surface, and is typically contacted with the dish surface for a period of time ranged from about 1 to about 10 seconds, although the actual time will vary with each application and user. The contacting of cloth, sponge, or similar article to the dish surface is preferably accompanied by a concurrent scrubbing of the dish surface.

Another method of the present invention will comprise immersing the soiled dishes into a water bath or held under running water without any liquid dishwashing detergent. A device for absorbing liquid dishwashing detergent, such as a sponge, is placed directly into a separate quantity of undiluted liquid dishwashing composition for a period of time typically ranging from about 1 to about 5 seconds. The absorbing device, and consequently the undiluted liquid dishwashing composition, is then contacted individually to the surface of each of the soiled dishes to remove said soiling. The absorbing device is typically contacted with each dish surface for a period of time range from about 1 to about 10 seconds, although the actual time of application will be dependent upon factors such as the degree of soiling of the dish. The contacting of the absorbing device to the dish surface is preferably accompanied by concurrent scrubbing.

Alternatively, the device may be immersed in a mixture of the hand dishwashing composition and water prior to being contacted with the dish surface, the concentrated solution is made by diluting the hand dishwashing composition with water in a small container that can accommodate the cleaning device at weight ratios ranging from about 95:5 to about 5:95, preferably about 80:20 to about 20:80 and more preferably about 70:30 to about 30:70, respectively, of hand dishwashing liquid: water respectively depending upon the user habits and the cleaning task.

The dimensions and values disclosed herein are not to be understood as being strictly limited to the exact numerical values recited. Instead, unless otherwise specified, each such dimension is intended to mean both the recited value and a functionally equivalent range surrounding that value. For example, a dimension disclosed as "40 mm" is intended to mean "about 40 mm."