Fabric softener active compositions

Abstract

The present invention relates to fabric softener active compositions comprising a combination of a quaternary ester ammonium compound and fatty solvents (a fatty acid ester, a fatty acid, a fatty alcohol and mixtures thereof) and methods of making and using the same. The invention also proposes fabric softener compositions, comprising the previously described active compositions, and methods of making and using the same.

Claims

1. A fabric softener active composition comprising: a component (a), said component comprising: at least one quaternary mono-ester ammonium compound, at least one quaternary di-ester ammonium compound and at least one quaternary tri-ester ammonium compound, and being obtainable by a process comprising at least the following steps: i) reacting a fatty acid, a methyl ester or a triglyceride thereof with an alkanolamine, wherein the molar ratio of fatty acid to alkanolamine is 1.4-2.5, to obtain a mixture containing an esteramine; and ii) quaternizing the mixture with an alkylating agent; a component (b), said component being a fatty acid ester or a mixture of fatty acid esters, wherein the component (b) content is in the range from 5 to 30% wt. based on the total weight of the fabric softener active composition; a component (c), said component being a fatty acid or a mixture of fatty acids, wherein the component (c) content is in the range from 0.5 to 15% wt. based on the total weight of the fabric softening active composition; wherein less than 3% by wt. of the total weight of the fabric softener active composition is a solvent; and wherein the composition has a dropping point below 60° C.

2. The fabric softener active composition according to claim 1, wherein the content of nitrogenated species in the component (a) is 65% wt. or more based on the total weight of the fabric softener active composition.

3. The fabric softener active composition according to claim 1, wherein in step i), the fatty acid, methyl ester or triglyceride thereof is/are reacted with an alkanolamine until the acid value is below 2 mg KOH/g.

4. The fabric softener active composition according to claim 1, wherein component (a) comprises at least one quaternary mono-ester ammonium compound of formula (I1), at least one quaternary di-ester ammonium compound of formula (I2), and at least one quaternary tri-ester ammonium compound of formula (I3), ##STR00002## wherein m=n=p=2; R.sub.1—C(O)— is a linear acyl group, wherein R.sub.1 is a linear alkyl or a linear alkenyl containing from 11 to 21 carbon atoms; R.sub.2 and R.sub.3 each represent —OH, q is 0; X.sub.1 is a methyl group; and A.sup.− is selected from a halide, phosphate or alkylsulphate.

5. The fabric softener active composition according to claim 1, wherein the component (b) content is in the range from 8 to 30% wt. based on the total weight of the fabric softener active composition.

6. The fabric softener active composition according to claim 1 wherein either the component (b) is a fatty acid methyl ester or a mixture of fatty acid methyl esters, or a fatty acid ethyl ester or a mixture of fatty acid ethyl esters; or the component (b) is a fatty acid ester or a mixture of fatty acid esters derived from a C.sub.12-C.sub.18 fatty alcohol or a mixture of C.sub.12-C.sub.18 fatty alcohols.

7. The fabric softener active composition according to claim 1 wherein the component (c) is a C.sub.12-C.sub.18 fatty acid or a mixture of C.sub.12-C.sub.18 fatty acids.

8. The fabric softener active composition according to claim 1 wherein the component (a), the component (b), the component (c) are derived from the same fatty acid.

9. The fabric softener composition of claim 1, wherein the solvent content is less than 2% by weight of the total weight of the fabric softener active composition.

10. A method to obtain a fabric softener active composition as defined in claim 1 comprising: i) an esterification step, wherein a fatty acid or a methyl ester or a triglyceride thereof is reacted with an alkanolamine, wherein the molar ratio of fatty acid to alkanolamine is from 1.4:1 to 2.5:1, to obtain a mixture containing an esteramine; and ii) a quaternization step, wherein the mixture obtained after the esterification step is reacted with an alkylating agent.

11. The method according to claim 10, wherein in step i), the fatty acid, methyl ester or triglyceride thereof is/are reacted with an alkanolamine until the acid value is below 2 mg KOH/g.

12. The method according to claim 10, wherein the quaternization reaction takes place in a degree from 60 to 95% of the totality of the reaction.

13. The method according to claim 10, wherein the component (b) present in the fabric softener active composition is intentionally added and/or generated in situ in the esterification step, after the esterification step, in the quaternization step or after the quaternization step.

14. The method according to claim 10 wherein the fabric softener active composition further comprises a component (d), said component being a fatty alcohol or a mixture of fatty alcohols, wherein the component (d) content is higher than 0% wt. and lower than 20% wt. based on the total weight of the fabric softener active composition, and wherein the component (b) is generated in situ by reaction with the component (d) which is added in the esterification step, after the esterification step, in the quaternization step or after the quaternization step.

15. The method according to claim 10, wherein component (c) present in the fabric softener active composition is intentionally added in the esterification step, after the esterification step, in the quaternization step or after the quaternization step.

16. A fabric softener composition comprising a fabric softener active composition as defined in claim 1, further comprising at least water, wherein the fabric softener active composition is present in an amount from 1 to 30% wt. based on the total weight of the fabric softener composition.

17. A method of conditioning a textile fabric, comprising the step of immersing the textile fabric in an aqueous bath comprising the fabric softener composition as defined in claim 16.

18. A method to obtain the fabric softener composition as defined in the claim 16, comprising the steps: i) adding the fabric softener active composition mixture to water; ii) stirring to obtain a homogeneous dispersion.

19. The method according to claim 18, comprising the steps: i) mixing in the molten state of the fabric softener active composition with the further components: from 0 to 2% of an electrolyte concentration aid; and/or from 0.01 to 3% of a thickening polymer; and/or from 0.01 to 5% of a perfume; ii) adding the obtained mixture to water; iii) stirring to obtain a homogeneous dispersion; and iv) cooling down.

Description

DETAILED DESCRIPTION OF THE INVENTION

(1) Fabric Softener Active Composition

(2) The main object of the present invention is a fabric softener active composition comprising: a component (a), said component comprising at least one or more quaternary mono-, di- or tri-ester ammonium compounds; a component (b), said component being a fatty acid ester or a mixture of fatty acid esters, wherein the component (b) content is in the range from 5 to 30% wt. based on the total weight of the fabric softener active composition; a component (c), said component being a fatty acid or a mixture of fatty acids, wherein the component (c) content is in the range from 0.5 to 15% wt. based on the total weight of the fabric softening active composition.

(3) Preferably, the fabric softener active composition according to the present invention comprises: a component (a), said component comprising at least one or more quaternary mono-, di- or tri-ester ammonium compounds of formula (I1), (I2), (I3), wherein the content of nitrogenated species in the component (a) is in the range from 65 to 95% wt. based on the total weight of the fabric softener active composition; a component (b), said component being a fatty acid ester or a mixture of fatty acid esters, wherein the component (b) content is in the range from 5 to 30% wt. based on the total weight of the fabric softener active composition, preferably from 8 to 30% wt., more preferably from 12 to 30% wt.; a component (c), said component being a fatty acid or a mixture of fatty acids, wherein the component (c) content is in the range from 0.5 to 15% wt. based on the total weight of the fabric softening active composition, preferably from 1 to 15% wt., more preferably from 2 to 15% wt.; optionally a component (d), said component being a fatty alcohol or a mixture of fatty alcohols, wherein the component (d) content is in the range from 0 to 20% wt. based on the total weight of the fabric softening active composition, preferably from 2 to 10% wt., more preferably from 2 to 5% wt.

(4) More preferably, the fabric softener active composition according to the present invention comprises: a component (a), said component comprising at least one or more quaternary mono-, di- or tri-ester ammonium compounds, wherein the content of nitrogenated species in the component (a) is in the range from 65 to 95% wt. based on the total weight of the fabric softener active composition; a component (b), said component being a fatty acid ester or a mixture of fatty acid esters, wherein the component (b) content is in the range from 5 to 30% wt. based on the total weight of the fabric softener active composition; a component (c), said component being a fatty acid or a mixture of fatty acids, wherein the component (c) content is in the range from 0.5 to 15% wt. based on the total weight of the fabric softening active composition.
(a): Quaternary Ester Ammonium Compound:

(5) The fabric softener active composition of the present invention comprises a component (a), said component comprising at least one or more quaternary mono-, di- or tri-ester ammonium compounds (commonly known as mono-esterquat (mono-EQ), di-esterquat(di-EQ), tri-esterquat (tri-EQ)) of formula (I1), (I2), (I3), wherein the content of nitrogenated species in the component (a) is in the range from 65 to 95% wt. based on the total weight of the fabric softener active composition:

(6) ##STR00001##
wherein in formulae (I1), (I2), (I3) R.sub.2 and R.sub.3 each independently represent —H or —OH; X.sub.1 represents a hydroxyalkyl group containing 1 to 4 carbon atoms, an alkyl group containing 1 to 4 carbon atoms or an alkyl group containing one aromatic group; R.sub.1 is a linear or branched alkyl containing 5 to 23 carbon atoms or a linear alkenyl group containing 5 to 23 carbon atoms and from 1 to 3 double bonds. In formulae I1, I2 and I3 each R.sub.1 can independently represent the same or different linear or branched alkyl chain; A.sup.− represents an anion; L represents a —(OCH.sub.2CH.sub.2).sub.a—(OCHR.sub.4CH.sub.2).sub.b— group, wherein R.sub.4 represents an alkyl group containing 1 to 4 carbon atoms, a represents a number within the range of 0 to 20, b represents a number within the range of 0 to 6, and the sum of a+b represents the average alkoxylation degree which corresponds to a number from 0 to 26; m, n, p each independently represents a number within the range from 1 to 4, q represents a number within the range from 0 to 26.

(7) The quaternary ester ammonium compounds of the invention can be ethoxylated and/or propoxylated, since a and b can be larger than 0. The order of sequence of the ethylene oxide and propylene oxide groups is not critical for the invention.

(8) In the case q is 2 or larger, each L group may be the same or different. Also the (L)q groups contained in the different branches within the compounds of formula (I1), (I2), (I3) may independently represent different meanings.

(9) The sum of a+b preferably represents the average alkoxylation degree which corresponds to a number from 0 to 10, more preferably from 0 to 6, most preferred is 0.

(10) Preferably, X.sub.1 is an alkyl group; more preferably X.sub.1 is a methyl group.

(11) Preferably, A.sup.− is selected from a halide, phosphate or alkylsulphate.

(12) Within the present patent application, when a numerical range is indicated, all the individual numbers included in said range are intended to be included. The same shall apply to any other range indicated.

(13) In a particularly preferred embodiment, the component (a) comprises at least one quaternary mono-ester ammonium compound of formula (I1), at least one quaternary di-ester ammonium compound of formula (I2), and at least one quaternary tri-ester ammonium compound of formula (I3), wherein m=n=p=2; R.sub.1—C(O)— is a linear acyl group wherein R.sub.1 is a linear alkyl or a linear alkenyl containing from 11 to 21 carbon atoms, preferably derived from (hydrogenated and/or non-hydrogenated) tallow fatty acid or palm fatty acid; R.sub.2 and R.sub.3 each represent —OH, q is 0 (i.e. the compound is not alkoxyated); X.sub.1 is a methyl group; and A.sup.− is selected from a halide, phosphate or alkylsulphate, preferably alkylsulphate.

(14) In another embodiment of the present invention, the component (a) comprises at least one or more quaternary mono-, di- or tri-ester ammonium compounds represented by formula (I1), (I2), (I3) as defined above, wherein R.sub.2 and R.sub.3 independently represent —OH; each m, n, p represents number 2.

(15) The rest of variables have the meanings as indicated above for formula (I1), (I2), (I3).

(16) In another embodiment of the present invention, R.sub.1 is a linear or branched alkyl containing 5 to 23 carbon atoms or a linear alkenyl group containing 5 to 23 carbon atoms and from 1 to 3 double bonds; preferably, the alkyl or alkenyl group contains from 11 to 21 carbon atoms.

(17) As used herein, the term “alkyl” refers to a straight or branched hydrocarbon chain containing from 1 to 23, preferably 5 to 23 carbon atoms.

(18) As used herein, the term “alkenyl” refers to a linear hydrocarbon chain containing from 2 to 23, preferably 5 to 23 carbon atoms and from one to 3 unsaturations.

(19) Linear or branched alkyl or linear alkenyl groups can originate from fatty acids, or methyl esters/triglycerides thereof, are alkyls or alkenyls derived from oils and fats from plants and animals, such as palm, palm kernel, coconut, rapeseed, sunflower, soybean, olive, canola, tall or tallow, possibly totally or partially hydrogenated and purified. Synthetic fatty acids, or methyl esters/triglycerides thereof, such as palmitoleic acid, oleic acid, elaidinic acid, petroselinic acid, linoleic acid, linolenic acid, stearic acid, myristic acid, gadoleic acid, behenic acid and erucic acid, or mixtures thereof, can also be employed in the present invention. Preferably, the linear or branched alkyl or linear alkenyl groups proceed from fatty acids derived from palm oil, coconut oil, tallow and hydrogenated tallow, more preferably from tallow or palm and hydrogenated tallow or palm.

(20) The fatty acid is preferably a C11-C21 acid containing a degree of unsaturation such that the iodine value (“IV”) is in the range from 0 to 100, preferably from 10 to 90, more preferably in the range from 15 to 85, most preferably 15 to 55.

(21) The fatty acid employed in the present invention have a cis to trans isomer ratio from 80:20 to 95:5. Preferably, the trans isomer content of said fatty acid is less than 10%.

(22) As used herein, the term “alkyl group containing one aromatic group” refers to the alkyl group as defined above, substituted by one aromatic group, wherein “aromatic group” refers to an aryl or heteroaryl group.

(23) “Aryl” refers to aromatic ring systems comprising 6 to 14 carbon atoms, more particularly 6 to 10, even more particularly 6 carbon atoms. Examples of aryl groups are phenyl, naphthyl, indenyl, fenanthryl or anthracyl radical, preferably phenyl or naphthyl radical. Said aryl radical may be optionally substituted by one or more substituents such as hydroxy, mercapto, halo, alkyl, phenyl, alkoxy, haloalkyl, nitro, cyano, dialkylamino, aminoalkyl, acyl and alkoxycarbonyl, as defined herein.

(24) “Alkoxy” refers to an alkyl group as defined above bonded to an oxygen atom (R—O—).

(25) Examples of halogen atoms are Br, Cl, I and F.

(26) The term “heteroaryl” means a monocyclic- or polycyclic aromatic ring comprising carbon atoms, hydrogen atoms, and one or more heteroatoms, preferably, 1 to 3 heteroatoms, independently selected from nitrogen, oxygen, and sulfur. The heterorayl group has 3 to 15 members and preferably 4 to 8 members. Illustrative examples of heteroaryl groups include, but are not limited to, pyridinyl, pyridazinyl, pyrimidyl, pyrazyl, triazinyl, pyrrolyl, pyrazolyl, imidazolyl, (1,2,3)- and (1,2,4)-triazolyl, pyrazinyl, pyrimidinyl, tetrazolyl, furyl, thienyl, isoxazolyl, thiazolyl, phenyl, isoxazolyl, and oxazolyl. A heteroaryl group can be unsubstituted or substituted with one or two suitable substituents such as hydroxy, mercapto, halo, alkyl, phenyl, alkoxy, haloalkyl, nitro, cyano, dialkylamino, aminoalkyl, acyl and alkoxycarbonyl, as defined herein. Preferably, a heteroaryl group is a monocyclic ring, wherein the ring comprises 2 to 5 carbon atoms and 1 to 3 heteroatoms.

Preparation of Quaternary Ester Ammonium Compound

(27) The component (a) comprises at least one or more quaternary mono-, di- or tri-ester ammonium compounds according to the invention. The component (a) can be prepared by i) esterification, reacting a fat source, preferably a fatty acid or a methyl ester/triglyceride thereof, with an alkanolamine (for example, but not limited to, triethanolamine, methyldiethanolamine or dimethylethanolamine) to obtain a mixture containing an esteramine, and ii) subsequently quaternizing the mixture with an alkylating agent.

(28) i) Esterification Step:

(29) It is preferred that the fat source employed in the esterification step is a fatty acid or a mixture of fatty acids. In case a fatty acid methyl ester or a fatty acid triglyceride is used, the transesterification conditions are those described in the state of the art.

(30) The reaction between the fatty acid and the alkanolamine is an esterification which leads to the formation of an esteramine or a mixture of esteramines, and it may be conducted in a known way, as described for example in document ES-A-2021900. Preferably the esterification reaction is carried out at a temperature between 150 and 200° C., for a period of 2-10 hours, preferably at a reduced pressure of about 5 to 200 mbar and in the presence of one of the catalysts known for the esterification, such as hypophosphorous acid or paratoluenesulfonic acid, and also in the presence of any of the usual stabilizers and antioxidants such as tocopherols, BHT, BHA, etc.

(31) In an embodiment of the present invention, a fatty alcohol or a mixture of fatty alcohols is additionally added to the system in the esterification step. A part of the fatty acid present in the system may react with a fatty alcohol resulting in a fatty acid fatty alcohol ester, as a further product of the esterification step, formed in addition to the esteramine/s. Suitable fatty alcohol is a C.sub.6-C.sub.24 alcohol or alkoxylated alcohol, or polyol, preferably a C.sub.12-18 alcohol.

(32) The molar ratio of fatty acid to alkanolamine is from 1.4:1 to 2.5:1, preferably from 1.6:1 to 2.2:1.

(33) The product resulting from the esterification reaction comprises a at least one or more mono-, di- and tri-esters of fatty acids. The product may also contain free alkanolamine, free fatty acid and free fatty alcohol. The progress of the reaction may be monitored by non-aqueous potentiometric titration with KOH.

(34) ii) Quaternization step:

(35) The quaternization of the esterification reaction product of alkanolamine with the fatty acid is conducted in a known way, as described for example in WO-A-9101295. Preferred alkylating agents include, but are not limited to, methyl chloride, dimethyl sulphate or mixtures thereof.

(36) The quaternization may take place in bulk or in solvent, at temperatures ranging from 40 to 90° C. If an added solvent is employed, then the starting materials and/or product must be soluble in the solvent to the extent necessary for the reaction (possible solvents can be the same solvents as used as component (b), component (c) and component (d) as defined below).

(37) The composition that results from the quaternization process comprises quaternised ester compounds having one (monoesterquat), two (diesterquat) or three (triesterquat) ester groups. The product may also contain quaternised alkanolamine, unreacted esteramine, unreacted fatty acid, as well a fatty acid alkyl ester, preferably a fatty acid methyl ester or a fatty acid ethyl ester.

(38) In an embodiment of the present invention, the component (a), said component comprising at least one or more quaternary mono-, di- or tri-ester ammonium compounds of formula (I1), (I2), (I3), is obtained from an esteramine mixture obtained by esterification of triethanolamine and tallow and/or hydrogenated tallow fatty acid and palm fatty acid followed by quaternization.

(39) The quaternization reaction may take place in a degree from 60 to 95% of the totality of the reaction.

(40) Preparation of the component (a) is carried out under conditions according to the person skilled in the art to obtain a mixture of at least one or more quaternary mono-, di- or tri-ester ammonium compounds of formula (I1), (I2), (I3).

(41) In an embodiment of the present invention, the component (a) comprises at least one or more quaternary mono-, di- or tri-ester ammonium compounds of formula (I1), (I2), (I3), wherein m=n=p; R.sub.1—C(O)— is a linear acyl group wherein R.sub.1 is an alkyl or alkenyl group containing from 11 to 21 carbon atoms, preferably derived from (hydrogenated or non-hydrogenated) tallow fatty acid or palm fatty acid; R.sub.2 and R.sub.3 each represent —OH, q is 0 (i.e. the compound is not ethoxylated); X.sub.1 is a methyl group; and A.sup.− is selected from a halide, phosphate or alkylsulphate, preferably alkylsulphate. Such compound may be produced by esterifying (hydrogenated and/or non-hydrogenated) tallow fatty acid or palm fatty acid and triethanolamine, wherein the ratio of tallow fatty acid or palm fatty acid to triethanolamine is from 1.6:1 to 2.2:1, and subsequently methylating the esteramine obtained thereby.

(42) (b): Fatty Acid Ester

(43) The fabric softener active composition of the present invention comprises a component (b), said component being a fatty acid ester or a mixture of fatty acid esters, wherein the component (b) content is in the range from 5 to 30% wt. based on the total weight of the fabric softener active composition, preferably from 8 to 30% wt more preferably from 12 to 30% wt.

(44) The component (b) present in the fabric softener active composition is intentionally added in the esterification step, after the esterification step, in the quaternization step, or after the quaternization step and/or generated in situ in the esterification step or in the quaternization step.

(45) In one embodiment of the present invention, the component (b) present in the fabric softener active composition is obtained in the quaternization step by the reaction between the unesterified fatty acid or a fatty acid additionally added into the system after the esterification step and the alkylating agent.

(46) In another embodiment of the present invention, the component (b) present in the fabric softener active composition is obtained in the esterification step by the reaction between the fatty acid or the mixture of fatty acids and a fatty alcohol or a mixture of fatty alcohols additionally added into the system.

(47) In another embodiment of the present invention, the component (b) present in the fabric softener active composition is added to the system after the esterification step has finished, and can act as a solvent for the quaternization step.

(48) In another embodiment of the present invention, the component (b) present in the fabric softener active composition is added to the component (a) after the quaternization step as an additive.

(49) Yet in another embodiment of the present invention, the component (b) present in the fabric softener active composition corresponds to the combination of the previously described embodiments.

(50) In one preferred embodiment of the invention, the component (b) has the following formula (I4):
R.sub.5—COO—R.sub.6  (I4)
wherein R.sub.5 represents a fatty acid moiety being a linear or branched alkyl containing 5 to 23 carbon atoms or a linear alkenyl group containing 5 to 23 carbon atoms and from 1 to 3 double bonds. Preferably, the alkyl or alkenyl group contains from 11 to 21 carbon atoms. Preferably, the alkyl or alkenyl group proceeds from fatty acids derived from palm oil, coconut oil, tallow and hydrogenated tallow, more preferably from tallow or palm and hydrogenated tallow or palm. R.sub.6 represents an alkyl or alkenyl group derived from a linear or branched, possibly alkoxylated (etoxylated, propoxylated, butoxylated), alcohol containing 1 to 24 carbon atoms.

(51) In another embodiment of the present invention, the component (b) is derived from: i) polyols, such as glycerol, sorbitol, pentaerythritol, etc. or ii) low or polymeric glycols, such as ethylene glycol, propylene glycol, dipropylene glycol, polyethylene glycol, polypropylene glycol, etc.

(52) In another embodiment of the present invention, the fatty acid moieties in the component (b) and the component (a) are derived from the same fatty acid.

(53) In another embodiment of the present invention, the component (b) is a fatty acid methyl ester or a mixture of fatty acid methyl esters, or a fatty acid ethyl ester or a mixture of fatty acid ethyl esters, preferably a fatty acid methyl ester or or a mixture of fatty acid methyl esters.

(54) In another embodiment of the present invention, the component (b) is a a fatty acid ester or a mixture of fatty acid esters derived from a C.sub.12-C.sub.18 fatty alcohol or a mixture of C.sub.12-C.sub.18 fatty alcohols.

(55) In another embodiment of the present invention, the alkyl or alkenyl group resulting from a linear or branched, possibly alkoxylated (etoxylated, propoxylated, butoxylated), alcohol containing 1 to 24 carbon atoms in component (b) is derived from a C.sub.12-18 fatty alcohol or a mixture of C.sub.12-C.sub.18 fatty alcohols.

(56) In yet another embodiment of the present invention, the component (b) present in the fabric softener active composition is a combination of a fatty acid methyl ester or a mixture of fatty acid methyl esters and a fatty acid ester or a mixture of fatty acid esters derived from a C.sub.12-C.sub.18 fatty alcohol or a mixture of C.sub.12-C.sub.18 fatty alcohols.

(57) (c): Fatty Acid

(58) The fabric softener active composition of the present invention comprises a component (c), said component being a fatty acid or a mixture of fatty acids, wherein the component (c) is in the range from 0.5 to 15% wt. based on the total weight of the fabric softening active composition, preferably from 1 to 15% wt., more preferably from 2 to 15% wt.

(59) The component (c) present in the fabric softener active composition is intentionally added in the esterification step, after the esterification step, in the quaternization step, or after the quaternization step and/or accounts for an unreacted material.

(60) In one embodiment of the present invention, the component (c) present in the fabric softener active composition corresponds to a free or unreacted fatty acid obtained after the esterification step which has not reacted with alkylating agent in the quaternization step to form a fatty acid methyl ester.

(61) In another embodiment of the present invention, the component (c) present in the fabric softener active composition corresponds to a fatty acid or a mixture of fatty acids added to the esterification product, before the quaternization step, and which has not reacted with alkylating agent in the quaternization step to result in a fatty acid methyl ester.

(62) In another embodiment of the present invention, the component (c) present in the fabric softener active composition is added to the component (a) after the quaternization step as an additive.

(63) Yet in another embodiment of the present invention, the component (c) present in the fabric softener active composition corresponds to the combination of the previously described embodiments.

(64) Suitable C6-C22 fatty acids are those obtained from vegetable and animal oils and fats such those obtained from castor oil, coconut oil, corn oil, mustard oil, olive oil, palm oil, peanut oil, rapeseed oil, sunflower oil, soybean oil, tall oil, tallow, eventually totally or partially hydrogenated, as well as purified or synthetic fatty acids, like caproic acid, caprylic acid, capric acid, isotridecanoic acid, lauric acid, myristic acid, palmitic acid, palmoleic acid, stearic acid, isostearic acid, 2-ethylhexanoic acid, oleic acid, elaidinic acid, petroselenic acid, linoleic acid, linolenic acid, eleostearic acid, ricinoleic acid, arachidic acid, gadoleic acid, behenic acid, erucic acid, or their technical-grade mixtures.

(65) In another embodiment of the present invention, the component (c) is a C.sub.12-C.sub.18 fatty acid or a mixture of C.sub.12-C.sub.18 fatty acids

(66) In another embodiment of the present invention, the component (c) and the component (a) are derived from the same fatty acid.

(67) The fatty acid is preferably a C12-C18 acid containing a degree of unsaturation such that the iodine value (“IV”) is in the range 0-90, preferably 10-90, more preferably in the range 15-85, most preferably 15-55.

(68) (d): Fatty Alcohol

(69) The fabric softener active composition of the present invention optionally comprises a component (d), said component being a fatty alcohol or a mixture of fatty alcohols, wherein the component (d) content is in the range from 0 to 20% wt. based on the total weight of the fabric softening active composition, preferably from 2 to 10% wt., more preferably from 2 to 5% wt.

(70) The component (d) present in the fabric softener active composition is intentionally added in the esterification step, after the esterification step, in the quaternization step, or after the quaternization step and/or accounts for an unreacted material.

(71) In one embodiment of the present invention, the component (d) present in the fabric softener active composition corresponds to a free or unreacted fatty alcohol that has not reacted with a fatty acid in the esterification step to form a fatty acid fatty alcohol ester.

(72) In another embodiment of the present invention, the component (d) present in the fabric softener active composition corresponds to a fatty alcohol or a mixture of fatty alcohols added to the esterification product as a quaternizing solvent.

(73) In another embodiment of the present invention, the component (d) present in the fabric softener active composition is added to the component (a) after the quaternization step as an additive.

(74) Yet in another embodiment of the present invention, the component (d) present in the fabric softener active composition corresponds to the combination of the previously described embodiments.

(75) Suitable fatty alcohol is a C6-C24 alcohol or alkoxylated (etoxylated, propoxylated, butoxylated) alcohol, or polyol, preferably a C12-18 alcohol.

(76) The fabric softener active composition according to the present invention may contain further components.

(77) (e): Solvent

(78) The present invention may further comprise a component (e), said component being a solvent. In a preferred embodiment, the component (e) content is lower than 8% wt. based on the total weight of the fabric softener active composition, preferably lower than 3% wt., more preferably lower than 2% wt.

(79) In the most preferred embodiment, the fabric softener active composition comprises essentially no solvent. The fabric softener active composition does not require the presence of a solvent to comply with the purpose of the invention.

(80) Solvents useful in the present technology include flammable liquids of flash point equal to or lower than 40° C. selected from the following list: methanol, ethanol, 1-propanol, 2-propanol, 1-butanol, 2-butanol, hexane, heptane, and combinations thereof. Preferably, the solvent is ethanol or 2-propanol and most preferably 2-propanol.

(81) Other suitable solvents for use in the present invention include ethylene glycol, trimethylene glycol, tetramethylene glycol, pentamethylene glycol, hexamethylene glycol, diethylene glycol, triethylene glycol, propylene glycol, dipropylene glycol and C1-C4 alkyl monoethers of ethylene glycol, propylene glycol, and dipropylene glycol, sorbitol, alkane diols such as 1,2-propanediol, 1,3-propanediol, 2,3-butanediol, 1,4-butanediol, 1,3-butanediol, 1,5-pentanediol, and 1,6 hexanediol; phenylethyl alcohol, 2-methyl-1,3-propanediol, hexylene glycol, sorbitol, polyethylene glycols, 1,2-hexanediol, 1,2-pentanediol, 1,2-butanediol, 1,4-cyclohexanedimethanol, pinacol, 2,4-dimethyl-2,4-pentanediol, 2,2,4-trimethyl-1,3-pentanediol (and ethoxylates), 2-ethyl-1,3-hexanediol, phenoxyethanol (and ethoxylates), glycol ethers, butyl carbitol, dipropylene glycol n-butyl ether, or combinations thereof.

(82) A method to obtain a fabric softener active composition according to the present invention comprises: i) an esterification step, wherein a fatty acid, a methyl ester or a triglyceride thereof is reacted with an alkanolamine to obtain a mixture containing an esteramine; and ii) a quaternization step, wherein the mixture obtained after the esterification step is reacted with an alkylating agent.

(83) Preferably, a C.sub.12-C.sub.18 fatty alcohol is added in the esterification step, after the esterification step, in the quaternization step or after the quaternization step. Even more preferably, a fatty acid, a methyl ester or a triglyceride thereof is added in the quaternization step or after the quaternization step.

(84) The term “added in the esterification/quaternization step” as used herein refers to addition of the respective component to the esterification/quaternization reaction mixture either prior to or in course of the esterification/quaternization reaction.

(85) The method to obtain a fabric softener active composition according to the present invention is characterized in that the component (b) present in the fabric softener active composition is intentionally added in the esterification step, after the esterification step, in the quaternization step or after the quaternization step and/or generated in situ in the esterification step or in the quaternization step. Preferably, the method to obtain a fabric softener active composition according to the present invention may be further characterized in that the component (c) present in the fabric softener active composition is intentionally added in the esterification step, after the esterification step, in the quaternization step or after the quaternization step and/or corresponds to an unreacted material. Even more preferably, the method to obtain a fabric softener active composition according to the present invention may be further characterized in that the component (d) present in the fabric softener active composition is intentionally added in the esterification step, after the esterification step, in the quaternization step or after the quaternization step and/or corresponds to an unreacted material.

(86) The fabric softener active composition of the present invention comprises: a component (a), said component comprising at least one or more quaternary mono-, di- or tri-ester ammonium compounds of formula (I1), (I2), (I3), wherein the content of nitrogenated species in the component (a) is in the range from 65 to 95% wt. based on the total weight of the fabric softener active composition; a component (b), said component being a fatty acid ester or a mixture of fatty acid esters, wherein the component (b) content is in the range from 5 to 30% wt. based on the total weight of the fabric softener active composition, preferably from 8 to 30% wt., more preferably from 12 to 30% wt.; a component (c), said component being a fatty acid or a mixture of fatty acids, wherein the component (c) content is in the range from 0.5 till 15% wt. based on the total weight of the fabric softening active composition, preferably from 1 till 15% wt., more preferably from 2 till 15% wt.; a component (d), said component being a fatty alcohol or a mixture of fatty alcohols, wherein the component (d) content is in the range from 0 to 20% wt. based on the total weight of the fabric softening active composition, preferably from 2 to 10% wt., more preferably from 2 to 5% wt.

(87) In one embodiment of the present invention, the component (a) comprises at least one quaternary mono-ester ammonium compound of formula (I1), at least one quaternary di-ester ammonium compound of formula (I2), and at least one quaternary tri-ester ammonium compound of formula (I3), wherein m=n=p=2; R.sub.1—C(O)— is a linear acyl group wherein R.sub.1 is a linear alkyl or alkenyl containing from 11 to 21 carbon atoms, preferably derived from (hydrogenated or non-hydrogenated) tallow fatty acid or palm fatty acid; R.sub.2 and R.sub.3 each represent —OH, q is 0 (i.e. the compound is not alkoxyated); X.sub.1, is a methyl group; and A.sup.− is selected from a halide, phosphate or alkylsulphate, preferably alkylsulphate. Such a compound may be produced by esterifying tallow fatty acid and triethanolamine, wherein the molar ratio of tallow fatty acid to alkanolamine is 1.4-2.5, preferably 1.6-2.2, and subsequently methylating the esteramine obtained thereby, wherein the degree of quaternization is from 25 to 95%.

(88) In another embodiment of the present invention, the component (b) is a C12-18 fatty acid ester, a C12-C18 fatty acid methyl/ethyl ester, preferably a C12-C18 fatty acid methyl ester, or mixtures thereof, wherein the fatty acid source is preferably palm oil, coconut oil, tallow and hydrogenated tallow, more preferably palm oil or tallow and hydrogenated tallow.

(89) In another embodiment of the present invention, the component (c) is preferably a C12-C18 fatty acid containing a degree of unsaturation such that the iodine value (“IV”) is in the range 15-55.

(90) In another embodiment of the present invention, the component (d) is a C12-18 fatty alcohol.

(91) In another embodiment of the present invention, the fabric softener active composition further comprises a component (e), said component being a solvent, wherein the solvent content is higher than 0% and lower than 8% wt. based on the total weight of the fabric softener active composition, preferably lower than 3% wt., more preferably lower than 2% wt.

(92) In another embodiment of the present invention, the component (e) is chosen from ethanol, 1-propanol and 2-propanol. The component (d) is preferably ethanol or 2-propanol and most preferably 2-propanol.

(93) Yet in another embodiment of the present invention, the component (e) can further comprise glycols, preferably propylene glycol.

(94) In an embodiment of the present invention, the fabric softener active composition comprises, in the indicated amounts expressed as percentage by weight with respect to the total weight of the composition: at least one or more quaternary mono-, di- or tri-ester ammonium compounds of the component (a), 5 to 25% of the component b), 0.5 to 15% of the component c), 0 to 20% of the component d).

(95) In another embodiment of the invention, the fabric softener active composition comprises, in the indicated amounts expressed as percentage by weight with respect to the total weight of the composition: at least one or more quaternary mono-, di- or tri-ester ammonium compounds of the component (a), 5 to 25% of the component b), 0.5 to 15% of the component c), 0 to 20% of the component d), 0 to 8% of the component e).

(96) In a particularly preferred embodiment of the present invention, the fabric softener active composition comprises no component (e).

(97) In another embodiment of the present invention, the sum content of the component (a), the component (b) and the component (c) is in the range from 5 to 35% wt. based on the total weight of the fabric softener active composition, more preferably from 10 to 25% wt. Additionally, the ratio of the component (b), derived from a low molecular weight alcohol, and the component (c) is in the range from 30/70 to 70/30% wt., whereas the ratio of the component (b), derived from a fatty alcohol, alkoxylated or not, or a polyol, and the component (d) is in the range from 50/50 to 95/5% wt.

(98) In an embodiment of the present invention, the fabric softener active composition contains from 65 to 95% wt. of nitrogenated species based on the total weight of the fabric softener active composition.

(99) Fabric Softener Composition

(100) Another object of the present invention is a fabric softener composition comprising a fabric softener active composition that comprises a component (a), a component (b), a component (c), and optionally a component (d), further comprising at least water, wherein the fabric softener active composition is present in an amount from 1 to 30% wt. based on the total weight of the fabric softener composition, more preferably from 1.5 to 25% wt., most preferably from 2 to 20% wt.

(101) In one embodiment of the present invention, the fabric softener composition further comprises optional components. In referring to the optional components, without this having to be regarded as an exhaustive description of all possibilities, which, on the other hand, are well known to the person skilled in the art, the following may be mentioned: a) other products that enhance the performance of the softening compositions, such as silicones, amine oxides, anionic surfactants, such as lauryl ether sulphate or lauryl sulphate, amphoteric surfactants, such as cocoamidopropyl betaine or alkyl betaines, sulphosuccinates, polyglucoside derivatives, etc. b) stabilising products, such as salts of amines having a short chain, which are quaternised or non-quaternised, for example of triethanolamine, N-methyldiethanolamine, etc., and also non-ionic surfactants, such as ethoxylated fatty alcohols, ethoxylated fatty amines. c) products that improve viscosity control, such as inorganic salts, for example, calcium chloride, magnesium chloride, calcium sulphate, sodium chloride, etc.; products which can be used to reduce viscosity in concentrated compositions, such as compounds of the glycol type, for example, ethylene glycol, dipropylene glycol, polyglycols, etc.; thickening agents for diluted compositions, such as polymers, suitable polymers are water soluble or dispersible, preferably the polymers are cationic. Suitable cationic polymeric materials include cationic guar polymers, cationic cellulose derivatives, cationic potato starch, cationic polyacrylamides. Specially suitable are cross-linked water swellable cationic polymers. Those described polymers may also act as deposition aids. d) components for adjusting the pH, which is from 2.0 to 6.0, preferably from 2.5 to 4.0, such as any type of inorganic and/or organic acid, for example hydrochloric, sulphuric, phosphoric, citric acid etc. e) agents that improve soil release, such as the known polymers or copolymers based on terephthalates. f) preservatives, such as bactericides, for example, 1,2-benzisothiazolin-3-one, 5-chloro-2-methyl-4-isothiazolin-3-one and 2-methyl-4-isothiazolin-3-one, or their combinations, 2-bromo-2-nitropropane-1,3-diol, etc. g) other products such as antioxidants, colouring agents, perfumes, germicides, fungicides, anti-corrosive agents, anti-crease agents, opacifiers, optical brighteners, pearl lustre agents, etc.

(102) In a preferred embodiment of the present invention, the fabric softener composition comprises a perfume or a perfume microcapsule, wherein the perfume content is lower than 5% wt. based on the total weight of the fabric softener composition, preferably lower than 3% wt., more preferably lower than 2% wt.

(103) In a particularly preferred embodiment of the present invention, the fabric softener composition comprises: a) from 0 to 2% of an electrolyte concentration aid, preferably from 0.01 to 1%, more preferably from 0.02 to 0.5%; and/or b) from 0.01 to 3% of a thickening polymer, preferably from 0.02 to 1%, more preferably from 0.05 to 0.5%; and/or c) from 0.01 to 5% of a perfume, alternatively from 0.1 to 4% or from 0.2 to 4% of a neat perfume and optionally from 0.01 to 3%, preferably from 0.1 to 2%, more preferably from 0.3 to 1%, of a perfume microcapsule.

Preparation of Fabric Softener Composition

(104) The fabric softener composition of the present invention can be obtained following a conventional process of mixing the different components, well known by any skilled person. For example, the different components can be mixed in the molten state, added to the water and stirred to obtain a homogeneous dispersion and then cooled down. In a preferred process of obtention, perfume is added once the fabric softener active composition is dispersed in water and the blend is cooled down.

(105) Method for Conditioning Textiles

(106) The fabric softener composition according to the invention can be used in both a so-called non-rinse and a so-called rinse process, where a fabric softener composition as defined above is first diluted in an aqueous rinse bath solution. Subsequently, the laundered fabrics which have been washed with a detergent liquor and optionally rinsed in one or more inefficient rinse steps (“inefficient” in the sense that residual detergent and/or soil may be carried over with the fabrics) are placed in the rinse solution with the diluted composition. Of course, the fabric softener composition may also be incorporated into the aqueous bath once the fabrics have been immersed therein. Following that step, agitation is applied to the fabrics in the rinse bath solution causing the suds to collapse, and residual soils and surfactant are to be removed. The fabrics can then be optionally wrung before drying.

(107) The non-rinse/rinse process may be performed manually in a basin or bucket, in a non-automated washing machine, or in an automated washing machine. When hand washing is performed, the laundered fabrics are removed from the detergent liquor and wrung out. The fabric softener of the present invention is then added to fresh water and the fabrics are then, directly in case of the non-rinse process or after one or more optional inefficient rinse steps in case of the rinse process, rinsed in the water containing the composition according to the conventional rinsing habit. The fabrics are then dried using conventional means.

(108) The following examples are given in order to provide a person skilled in the art with a sufficiently clear and complete explanation of the present invention, but should not be considered as limiting of the essential aspects of its subject, as set out in the preceding portions of this description.

(109) The following examples are given in order to provide a person skilled in the art with a sufficiently clear and complete explanation of the present invention, but should not be considered as limiting of the essential aspects of its subject, as set out in the preceding portions of this description.

EXAMPLES

(110) The first part of the Examples section refers to the preparation of the fabric softener active compositions according to the invention.

(111) The second and third part of the Examples indicates analytical methods and physical properties methods, respectively, used to analyse the prepared fabric softener active compositions.

(112) The fourth part of the Examples section presents some fundamental physical-chemical characteristics of the prepared fabric softener active compositions: content of residual amine, content of fatty acid methyl ester, content of fatty acid ester, content of free fatty acid, content of fatty alcohol, dropping point, and melt viscosity.

(113) The fifth part of the Examples refers to the preparation of the fabric softener compositions according to the invention, the determination of the initial viscosity of the aqueous dispersions and to the performance evaluation of their softening properties.

1. Preparation of the Fabric Softener Active Compositions According to the Invention

(114) Selected examples correspond to the fabric softener active compositions based on tallow fatty acids at different hydrogenation degrees.

Example 1

(115) Esterification

(116) 1800 grams (6.62 mol) of tallow fatty acid and 600 grams (2.21 mol) of hydrogenated tallow fatty acid were introduced in an inert atmosphere into a stainless steel reactor, and 796.8 grams (5.35 mol) of triethanolamine were added with stirring. The mixture was heated for at least 4 hours at 160-180° C. in order to remove water from the reaction. The final point of the reaction was monitored by an acid value assay, until the value was below 2 mg KOH/g.

(117) A yellowish liquid product from the esterification step was obtained, consisting essentially of a mixture of unesterified fatty acids, mono-, di- and triesterified triethanolamine and unreacted triethanolamine.

(118) Quaternization

(119) 40.7 grams (0.15 mol) of tallow fatty acid and 13.6 grams (0.05 mol) of hydrogenated tallow fatty acid were added with stirring to 852 grams of the product from the esterification step (containing 1.50 mol of esteramine). Then, 179.8 grams (1.43 mol) of dimethyl sulphate were added with stirring at a temperature of 50-90° C. After four hours of digestion, the virtually complete absence of amine value was verified by acid/base assay. 1087.2 grams of the product containing the quaternized esteramine were obtained.

Example 2

(120) Esterification

(121) 1800 grams (6.62 mol) of tallow fatty acid and 600 grams (2.21 mol) of hydrogenated tallow fatty acid were introduced in an inert atmosphere into a stainless steel reactor, and 796.8 grams (5.35 mol) of triethanolamine were added with stirring. The mixture was heated for at least 4 hours at 160-180° C. in order to remove water from the reaction. The final point of the reaction was monitored by an acid value assay, until the value was below 2 mg KOH/g.

(122) A yellowish liquid product from the esterification step is obtained, consisting essentially of a mixture of unesterified fatty acids, mono-, di- and triesterified triethanolamine and unreacted triethanolamine.

(123) Quaternization

(124) 86.35 grams (0.32 mol) of tallow fatty acid and 28.75 grams (0.11 mol) of hydrogenated tallow fatty acid were added with stirring to 855.6 grams of the product from the esterification step (containing 1.51 mol of esteramine). Then, 180.5 grams (1.44 mol) of dimethyl sulphate were added with stirring at a temperature of 50-90° C. After four hours of digestion, the virtually complete absence of amine value was verified by acid/base assay. 1152.4 grams of the product containing the quaternized esteramine were obtained.

Example 3

(125) Esterification

(126) 1500 grams (5.51 mol) of tallow fatty acid and 1500 grams (5.51 mol) of hydrogenated tallow fatty acid were introduced in an inert atmosphere into a stainless steel reactor, and 996 grams (6.68 mol) of triethanolamine were added with stirring. The mixture was heated for at least 4 hours at 160-180° C. in order to remove water from the reaction. The final point of the reaction was monitored by an acid value assay, until the value was below 2 mg KOH/g.

(127) A yellowish liquid product from the esterification step is obtained, consisting essentially of a mixture of unesterified fatty acids, mono-, di- and triesterified triethanolamine and unreacted triethanolamine.

(128) Quaternization

(129) 148.7 grams (0.55 mol) of tallow fatty acid and 148.7 grams (0.55 mol) of hydrogenated tallow fatty acid were added with stirring to 1435.8 grams of the product from the esterification step (containing 2.5 mol of esteramine). Then, 303.6 grams (2.4 mol) of dimethyl sulphate were added with stirring at a temperature of 50-90° C. After four hours of digestion, the virtually complete absence of amine value was verified by acid/base assay. 2038.8 grams of the product containing the quaternized esteramine were obtained.

Example 4

(130) Esterification

(131) 1800 grams (6.62 mol) of tallow fatty acid and 600 grams (2.21 mol) of hydrogenated tallow fatty acid were introduced in an inert atmosphere into a stainless steel reactor, and 796.8 grams (5.35 mol) of triethanolamine were added with stirring. The mixture was heated for at least 4 hours at 160-180° C. in order to remove water from the reaction. The final point of the reaction was monitored by an acid value assay, until the value was below 2 mg KOH/g.

(132) A yellowish liquid product from the esterification step is obtained, consisting essentially of a mixture of unesterified fatty acids, mono-, di- and triesterified triethanolamine and unreacted triethanolamine.

(133) Quaternization

(134) 24.6 grams (0.09 mol) of tallow fatty acid methyl ester were added with stirring to 304.2 grams of the product from the esterification step (containing 0.54 mol of esteramine). Then, 64.2 grams (0.51 mol) of dimethyl sulphate were added with stirring at a temperature of 50-90° C. After four hours of digestion, the virtually complete absence of amine value was verified by acid/base assay. Then 12.3 grams (0.05 mol) of tallow fatty acid and 4.1 grams (0.02 mol) of hydrogenated tallow fatty acid were added, obtaining a total of 409.4 grams of the final product.

Example 5

(135) Esterification

(136) 337.2 grams (1.24 mol) of tallow fatty acid and 337.2 grams (1.24 mol) of hydrogenated tallow fatty acid were introduced in an inert atmosphere into a stainless steel reactor, then 165.8 grams (1.11 mol) of triethanolamine, together with 81.2 grams (0.42 mol) of a fatty alcohol C.sub.12-14 (C.sub.12—OH 70%, C.sub.14—OH 30%) were added with stirring. The mixture was heated for at least 4 hours at 160-180° C. in order to remove water from the reaction. The final point of the reaction was monitored by an acid value assay, until the value was below 2 mg KOH/g.

(137) A yellowish liquid product from the esterification step was obtained, consisting essentially of a mixture of unesterified fatty acids, mono-, di- and triesterified triethanolamine, esterified fatty alcohols, unreacted triethanolamine and fatty alcohols.

(138) Quaternization

(139) 828.2 g of the product from the esterification step (containing 1.07 mol of esteramine) were reacted with 127.9 grams (1.01 mol) of dimethyl sulphate, which were added with stirring at a temperature of 50-90° C. After four hours of digestion, the virtually complete absence of amine value was verified by acid/base assay. A total of 956.1 grams of the final product were obtained.

Example 6

(140) Esterification

(141) 317.0 grams (1.17 mol) of tallow fatty acid and 317.0 grams (1.17 mol) of hydrogenated tallow fatty acid were introduced in an inert atmosphere into a stainless steel reactor, then 155.9 grams (1.05 mol) of triethanolamine, together with 76.3 grams (0.39 mol) of a fatty alcohol C.sub.12-14 (C.sub.12—OH 70%, C.sub.14—OH 30%) were added with stirring. The mixture was heated for at least 4 hours at 160-180° C. in order to remove the water of the reaction. The final point of the reaction was monitored by an acid value assay, until the value was below 2 mg KOH/g.

(142) A yellowish liquid product from the esterification step is obtained, consisting essentially of a mixture of unesterified fatty acids, mono-, di- and triesterified triethanolamine, esterified fatty alcohols, unreacted triethanolamine and fatty alcohols.

(143) Quaternization

(144) 23.7 grams (0.09 mol) of tallow fatty acid and 23.7 grams (0.09 mol) of hydrogenated tallow fatty acid were added with stirring to 778.5 grams of the product from the esterification step (containing 1.00 mol of esteramine). Then, 120.23 grams (0.95 mol) of dimethyl sulphate were added with stirring at a temperature of 50-90° C. After four hours of digestion, the virtually complete absence of amine value was verified by acid/base assay. A total of 946.0 grams of the final product were obtained.

2. Analytical Methods

(145) Potentiometric Acid/Base Titrations

(146) Content on amine salt and free fatty acid were determined by non-aqueous potentiometric titration with KOH. Samples were dissolved in 2-propanol.

(147) Total amine value was determined by non-aqueous potentiometric titration with perchloric acid solution in glacial acetic acid.

(148) Residual amine value, which corresponds to the non-quaternized amine fraction, was calculated as the sum of total amine value and amine salt.

(149) All these values are expressed as mg KOH per g.

(150) GLC Analysis

(151) Content of fatty acid methyl ester, fatty acid fatty alcohol ester and free fatty alcohol were determined by GLC analysis, using an internal standard. Samples were dissolved in chloroform.

3. Physical Properties Methods

(152) Dropping point was determined by the capillary method as the temperature at which the first drop falls or flows out of the standard cylindrical cup with a circular hole with a diameter of 2.8 mm in the bottom. Samples were melted and introduced in the cup. They were left to solidify between 12-24 hours in a refrigerator at a low temperature (−20° C.)(a initial temperature of at least 5° C. below the expected dropping point is required). Samples were then subjected to a constant heating rate (1° C./min) to the point when they flowed through the hole, corresponding to the dropping point.

(153) Melt viscosities were taken at 70° C. on a Rheometer Haake model RS600 at a shear rate of 5 s-1 using 60 mm serrated parallel plates with a plate distance of 0.8 mm.

4. Physical-Chemical Characteristics of the Prepared Fabric Softener Active Compositions

(154) Physical-chemical characteristics of the fabric softener active compositions, prepared as it has been described in the first part of the Examples section, are summarized in Table 1 below.

(155) TABLE-US-00001 TABLE 1 Examples Physical-chemical property 1 2 3 4 5 6 FA: Tallow/Hydrogenated 75/25 75/25 50/50 75/25 50/50 50/50 tallow ratio Residual amine value 14.6 16.6 20.7  7.4 8.2 12.5 (mg KOH/g) Fatty acid methyl ester (%) 3.5 5.7 7.3 6.0 0.5 2.8 Fatty acid fatty alcohol — — — — 12.5 12.8 ester (%) Free fatty acid (%) 2.1 6.1 8.1 4.4 0.5 3.5 Free fatty alcohol (%) — — — — 1.8 2.1 Dropping point (° C.) 64.1 48.0 53.8  46.9  51.1 48.2 Viscosity (cP) at 70° C. 3307 2376 931 .sup.  922 .sup.  622 315

(156) Examples 2 to 6 correspond to fabric softener active compositions within the scope of the invention, showing dropping points below 60° C. which will allow the handling at molten state at maximum 70° C., ensuring a good chemical stability. In the same way, all fabric softener active compositions according to the invention show moderate viscosity values at 70° C., so that they can be easily pumped in the molten state.

(157) Correspondingly, example 1 accounts for a fabric softener active composition not within the scope of the invention, since dropping point is above 60° C., which would demand a handling temperature overcoming 70° C., compromising the chemical stability of the product. Accordingly, the fabric softener active compositions within the scope of the invention have suitable viscosity at low content or in the absence of flammable solvents and at the same time.

5. Preparation of the Fabric Softener Compositions According to the Invention and Performance Evaluation of their Softening Properties

(158) Fabric softener compositions were made by dispersing fabric softener active compositions into water.

(159) Aqueous dispersions shown in Table 2 contain 4.5% of fabric softener active compositions and 0.1% active of a thickening polymer (i.e. FLOSOFT 222 manufactured by SNF).

(160) The dispersion process consists of heating deionized water at 60° C. in a jacketed glass reactor, adding the thickening polymer while stirring until complete incorporation, adding the fabric softener active composition of interest in the molten state (heated 5 to 10° C. above the melting point) and homogenizing the dispersion at a rate of 150 rpm during 20 min. The aqueous dispersion is finally cooled down up to 25-30° C., at rate of 1.0° C./min, maintaining the agitation at 150 rpm.

(161) Initial viscosity of the aqueous dispersions was determined at 20° C., 24 h after preparation, with a Brookfield viscosimeter model LV, using a spindle number 2 at 60 rpm.

(162) Softening performance of fabric softener compositions was determined by means of a sensorial test carried out by a panel of experts using pieces of terry cotton towel treated with the corresponding aqueous dispersions of the fabric softener active compositions.

(163) Fabric treatment consists of a consequtive sequence of washing and softening steps, carried out in hard water of 20° HF. Previously scoured terry cotton towels were washed at 40° C. with a heavy duty powder detergent (at a dosage of 2.7% on weight fabric), rinsed twice and spinning dried. Wet towels were treated for 10 minutes at 25° C. with the corresponding aqueous dispersions diluted in water to provide a dosage of 0.12% fabric softener active composition on weight fabric, for a bath ratio of 1/10. Treated cotton towels were finally spun dried and let dry by hanging, and left still for 24 hours under controlled atmospheric conditions (60% HR and 20° C.)

(164) Softening effect was determined by comparison in pairs, by 12 panellists, against standard products of equivalent hydrogenation degree (comparative examples C1 and C2). Results are indicated in Table 2. The comparative evaluation was made according to the following criteria: +2: softer than the reference +1: slightly softer than the reference 0 as soft as the reference −1: slightly harder than the reference −2: harder than the reference

(165) TABLE-US-00002 TABLE 2 Fabric softener active composition 2 3 4 5 6 C1 C2 Initial viscosity at 20° C. 180 260 185 135 260 90 115 (cP) Softening effect +1 +1 +1 +2 +1 — — compared to C1 C2 C1 C2 C2 — — C1: TETRANYL ®L1/90 available from Kao Corporation, Ester Quat with a tallow/hydrogenated tallow ratio of 75/25 C2: TETRANYL ®L2-90 available from Kao Corporation, Ester Quat with a tallow/hydrogenated tallow ratio 50/50

(166) It can be seen that all fabric softener active compositions within the scope of the invention provide higher viscosity values and higher softening effects than the fabric softener active compositions of the corresponding comparative examples.