WO1993001265A1 - Fabric softening composition - Google Patents

Fabric softening composition Download PDF

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Publication number
WO1993001265A1
WO1993001265A1 PCT/GB1992/001181 GB9201181W WO9301265A1 WO 1993001265 A1 WO1993001265 A1 WO 1993001265A1 GB 9201181 W GB9201181 W GB 9201181W WO 9301265 A1 WO9301265 A1 WO 9301265A1
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WIPO (PCT)
Prior art keywords
fabric softening
ester
quaternary ammonium
iodine value
linked
Prior art date
Application number
PCT/GB1992/001181
Other languages
French (fr)
Inventor
Graham Andrew Turner
Original Assignee
Unilever Plc
Unilever Nv
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Unilever Plc, Unilever Nv filed Critical Unilever Plc
Priority to CA002112816A priority Critical patent/CA2112816C/en
Priority to EP92913677A priority patent/EP0593542B1/en
Priority to US08/170,351 priority patent/US5407589A/en
Priority to JP05502058A priority patent/JP3076063B2/en
Priority to DE69213016T priority patent/DE69213016T2/en
Publication of WO1993001265A1 publication Critical patent/WO1993001265A1/en

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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C229/00Compounds containing amino and carboxyl groups bound to the same carbon skeleton
    • C07C229/02Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton
    • C07C229/04Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated
    • C07C229/24Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated having more than one carboxyl group bound to the carbon skeleton, e.g. aspartic acid
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/38Cationic compounds
    • C11D1/46Esters of carboxylic acids with amino alcohols; Esters of amino carboxylic acids with alcohols
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/38Cationic compounds
    • C11D1/62Quaternary ammonium compounds
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/38Cationic compounds
    • C11D1/645Mixtures of compounds all of which are cationic
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/66Non-ionic compounds
    • C11D1/835Mixtures of non-ionic with cationic compounds
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/0005Other compounding ingredients characterised by their effect
    • C11D3/001Softening compositions
    • C11D3/0015Softening compositions liquid
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/66Non-ionic compounds
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/66Non-ionic compounds
    • C11D1/72Ethers of polyoxyalkylene glycols

Definitions

  • This invention relates to a fabric softening material and to a method for its preparation.
  • the invention relates to a fabric softening composition for use in the rinse step of a fabric washing process.
  • Conventional rinse added fabric softening compositions contain fabric softening materials which are substantially water-insoluble cationic materials usually having two long alkyl chains. Typical of such materials are distearyl dimethyl ammonium chloride. These materials are usually prepared in the form of an aqueous dispersion or emulsion.
  • a problem with quaternary softener materials comprising ester linkages is that some tend to have a relatively high pour point.
  • Pour point can be defined as the lowest temperature at which a material can be observed to flow under specified conditions. (As explained in The Analysis of Fats and Oils by V C Mehlenbacher, The Garrard Press, Champaign, Illinois 1960) .
  • a high pour point renders the softener materials sometimes difficult to process.
  • the softener materials as described in US 4 137 180 (LEVER BROTHERS) have high pour points meaning that they are hardly pu pable at temperatures conventionally used in rinse conditioner manufacture, eg. 60°C, and are difficult to disperse in water.
  • ester-linked softening materials can be lowered by using a higher proportion of unsaturated substituents in each molecule compared with that normally used.
  • the man skilled in the art would expect a decrease in softening performance from such materials since this phenomenon is seen with conventional quaternaries having two long alkyl chains.
  • ester-linked quaternary ammonium compounds or their corresponding amines comprising a high proportion of unsaturated substituents in the molecule or mixture of molecules having unsaturated substituents with molecules having saturated substituents can give superior softening when compared to the softening performance obtained from saturated ester-linked quaternaries or their corresponding amines or non-ester-linked quaternaries.
  • the present invention provides a fabric softening material comprising an ester-linked a ine compound and/or its corresponding quaternary ammonium compound of general formula I
  • each R ⁇ group is independently selected from C 1-4 alkyl, alkenyl or hydroxyalkyl groups; and each R 2 group is independently selected from C 8-28 alkyl or alkenyl groups, n is an integer from 0 to 5 and m is an integer from 1 to 5; such that the material has an Iodine value of between 5 and 24.
  • fabric softening materials according to the invention can have a lower pour point than ester-linked materials of lower Iodine value and can give superior softening than ester-linked materials of lower Iodine value.
  • the fabric softening material comprises at least 80% by weight of ester-linked amine and/or quaternary ammonium compound, and more preferably at least 90% Most preferably the fabric softening material comprises between 80% and 95% by weight of ester-linked amine and/or quaternary ammonium compound.
  • the fabric softening materials of the invencion comprise an extender material selected from :
  • ester-linked quaternary ammonium compounds useful in the present invention are preferably prepared in the presence of more than a 10 mole % excess of alkyl or alkenyl groups as disclosed in EP 420 465 (Unilever) since this has also been found to lower the pour point of the compound.
  • the fabric softening material has an Iodine value between 5 and 20, most preferably between 5 and 15.
  • Iodine value as used in the context of the present invention refers to the measurement of the degree of unsaturation present in a material by a method of nmr spectroscopy as described in Anal. Che . , .34., 1136 (1962) Johnson and Shoolery.
  • Iodine value is defined as the number of grams of iodine absorbed per lOOg of the test material. Olefinic materials absorb 1 gram of iodine per atom of olefinic hydrogen. Hence measurement can be converted to the equivalent Iodine Value.
  • the hydrogen nmr spectrum at 360 MHz is obtained for the test material.
  • the integral intensity, I s of the band derived from olefinic hydrogen in the alkyl chain and the integral intensity, I m , of the band derived from terminal methyl groups in the alkyl chains are measured.
  • MMW is the mean molecular weight of the test material.
  • Preferred fabric softening materials comprise a 1:4 parts by weight mixture of 1,2 ditallowyl oxy-3-trimethylammoniopropane chloride made according to US 4 137 180 (Lever Bros.) with its dihardened tallowy1 counterpart.
  • a second aspect of the invention provides an aqueous fabric softening composition
  • a fabric softening material comprising an ester-linked amine compound of formula I and/or its corresponding quaternary ammonium compound wherein the compound comprises at least one unsaturated substituent such that the material has an Iodine value of between 5 and 24.
  • composition comprises from 5% to 80% by weight of fabric softening material, more preferably from 15% to 60% by weight.
  • Compositions of the invention are obtainable by heating the material to a temperature above 40°C followed by dispersing the material into water.
  • the materials are heated to a temperature of above 50°C and dispersed in water at elevated temperature.
  • compositions of the invention preferably have a pH of more than 2.0 and less than 8.0, more preferably less than 5.0. Especially preferred are pH values in the range of from 2.5 to 4.0.
  • compositions of the invention may in addition to the above ingredients also comprise other ingredients, such as non-aqueous solvents such as C 1-4 alkanols and polyhydric alcohols, pH-buffering agents such as weak acids e.g. phosphoric, benzoic or citric acids, re-wetting agents, viscosity modifiers, aluminium chlorohydrate, antigelling agents, perfumes, perfume carriers, hydrocarbons, fluorescers, colourants, hydrotropes, antifoa ing agents, antiredeposition agents, enzymes, optical brightening agents, opacifiers, stabilisers such as guar gum and polyethylene glycol, anti shrinking agents, anti-wrinkle agents, silicones, soil release agents, antioxidants, anti-corrosion agents, preservatives, dyes, bleaches, bleach precursors, drape-imparting agents, antistatic agents and ironing aids.
  • non-aqueous solvents such as C 1-4 alkanols and polyhydric alcohols
  • Example 1 The invention will be further illustrated by means of the following examples : Example 1
  • compositions were prepared by melting the required amounts of unsaturated compound and saturated compound, mixing and adding the premix to hot (70°C) demineralised water while stirring.
  • the softening performance of the monitors was tested by treating 40g of terry monitors with a 2ml dose of a 5% dispersion of the mix in 1 litre of water, line drying and assessing for softness using an expert panel and a round robin paired comparison technique.
  • Arquad 2T is ditallow dimethyl ammonium chloride ex Akzo Chemie.
  • Arquad 2HT is dihardened tallow dimethyl ammonium chloride ex Akzo Chemie.
  • compositions were prepared and softening assessed as described in Example 1.
  • a difference of 0.62 between scores indicates a significant difference at the 95% confidence limit.
  • T TMAPC is 1,2 ditallowyloxy-3-trimethylammoniopropane chloride ex Hoescht.
  • HT TMAPC is 1,2 dihardened tallowyloxy-3-trimethyl- am oniopropane chloride ex Hoescht.
  • dispersions of 4:1 mixtures of hardened tallow quaternary ammonium material to soft tallow quaternary ammonium material were prepared by co-melting the materials and adding the premix to hot water (70°C) with stirring. The dispersions were cooled to room temperature with stirring. 2ml of the dispersions were added to 1 of 14°FH water containing 0.001% of alkyl benzene sulphonate to simulate anionic carry over from the main wash. Three test monitors (40-50g terry towelling) were placed in the dispersions and agitated in a tergotometer (5 mins, 60rpm) . The monitors were line dried and softening assessed using a round robin paired comparison.
  • Rewoquat W75H is dihardened tallow imidazolinium quaternary.
  • Rewoquat W75 is ditallow imidazolinium quaternary.
  • Tetranyl AT-1 is N-methyl, N,N di( ⁇ -tallowyloxy ethyl) N ⁇ -hydroxyethyl ammonium chloride ex Kao.
  • Tetranyl AHT-1 is N-methyl N,N di ( ⁇ -hardened tallowyloxy ethyl) N ⁇ -hydroxyethyl ammonium chloride ex Kao.

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Wood Science & Technology (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

A fabric softening material comprising an ester-linked amine compound and/or its corresponding quaternary ammonium compound of general formula (I) where each R1 group is independently selected from C1-4 alkyl, alkenyl, or hydroxyalkyl groups; each R2 group is independently selected from C8-28 or alkenyl groups and n and m are integers from 1 to 5; such that the material has an Iodine value of between 5 and 24, preferably between 5 and 20. The invention also comprises an aqueous fabric softening composition containing the softening material.

Description

FABRIC SOFTENING COMPOSITION
This invention relates to a fabric softening material and to a method for its preparation. In particular the invention relates to a fabric softening composition for use in the rinse step of a fabric washing process.
Conventional rinse added fabric softening compositions contain fabric softening materials which are substantially water-insoluble cationic materials usually having two long alkyl chains. Typical of such materials are distearyl dimethyl ammonium chloride. These materials are usually prepared in the form of an aqueous dispersion or emulsion.
It has been proposed in EP 239 910 (PROCTER & GAMBLE) to incorporate ester linked quaternary ammonium compounds in fabric softening compositions. US 3 915 867 (STEPAN) discloses the use of N-methyl,N<N-di (beta-C14_18 acyloxyethyl) N-beta-hydroxy ethyl ammonium methosulphate in softening compositions. Other ester linked softener materials are described in US 4 137 180 (LEVER BROTHERS; . Softener materials comprising ester linkages are especially preferred for use in fabric conditioning compositions for environmental reasons.
A problem with quaternary softener materials comprising ester linkages is that some tend to have a relatively high pour point. Pour point can be defined as the lowest temperature at which a material can be observed to flow under specified conditions. (As explained in The Analysis of Fats and Oils by V C Mehlenbacher, The Garrard Press, Champaign, Illinois 1960) . A high pour point renders the softener materials sometimes difficult to process. For example, the softener materials as described in US 4 137 180 (LEVER BROTHERS) have high pour points meaning that they are hardly pu pable at temperatures conventionally used in rinse conditioner manufacture, eg. 60°C, and are difficult to disperse in water.
We have now found that the pour point of ester-linked softening materials can be lowered by using a higher proportion of unsaturated substituents in each molecule compared with that normally used. The man skilled in the art would expect a decrease in softening performance from such materials since this phenomenon is seen with conventional quaternaries having two long alkyl chains. Surprisingly we have found that ester-linked quaternary ammonium compounds or their corresponding amines comprising a high proportion of unsaturated substituents in the molecule or mixture of molecules having unsaturated substituents with molecules having saturated substituents can give superior softening when compared to the softening performance obtained from saturated ester-linked quaternaries or their corresponding amines or non-ester-linked quaternaries.
In EP 0 052 517 (PROCTER & GAMBLE) it is disclosed that pourable, concentrated fabric softener compositions can be obtained when the composition comprises a mixture of a mono nitrogen quaternary ammonium salt, a di(2-amidoethyl) methyl quaternary ammonium salt and an imidazolinium salt where the cationic system has an Iodine value of at least 4.2. In this prior art specification the 'pourability' is defined in terms of the finished composition and not the component parts. No mention of ester-linked quaternaries or improved softening performance is made. In JP 2169769A KAO CORP it is disclosed that softening and finishing agents for treating garments can comprise certain quaternary ammonium compounds with substituents having certain degrees of unsaturation.
Accordingly the present invention provides a fabric softening material comprising an ester-linked a ine compound and/or its corresponding quaternary ammonium compound of general formula I
R,
N (CH2)n CH (CH2)ra CH2COOR2 (I)
I I
Figure imgf000005_0001
where each Rα group is independently selected from C1-4 alkyl, alkenyl or hydroxyalkyl groups; and each R2 group is independently selected from C8-28 alkyl or alkenyl groups, n is an integer from 0 to 5 and m is an integer from 1 to 5; such that the material has an Iodine value of between 5 and 24.
The advantages of fabric softening materials according to the invention are that they can have a lower pour point than ester-linked materials of lower Iodine value and can give superior softening than ester-linked materials of lower Iodine value.
Preferably the fabric softening material comprises at least 80% by weight of ester-linked amine and/or quaternary ammonium compound, and more preferably at least 90% Most preferably the fabric softening material comprises between 80% and 95% by weight of ester-linked amine and/or quaternary ammonium compound. Preferably the fabric softening materials of the invencion comprise an extender material selected from :
(a) tertiary amine or quaternary ammonium compounds comprising one long alkyl or alkenyl group with more than ten carbon atoms;
(b) predominantly unbranched linear nonionic materials; and
(c) mixtures thereof
since these extender materials have also been found tc lower the pour point of ester-linked quaternary ammoniurr. compounds as disclosed in EP 409 504 (Unilever) .
The ester-linked quaternary ammonium compounds useful in the present invention are preferably prepared in the presence of more than a 10 mole % excess of alkyl or alkenyl groups as disclosed in EP 420 465 (Unilever) since this has also been found to lower the pour point of the compound.
Preferably the fabric softening material has an Iodine value between 5 and 20, most preferably between 5 and 15. Iodine value as used in the context of the present invention refers to the measurement of the degree of unsaturation present in a material by a method of nmr spectroscopy as described in Anal. Che . , .34., 1136 (1962) Johnson and Shoolery.
Iodine value is defined as the number of grams of iodine absorbed per lOOg of the test material. Olefinic materials absorb 1 gram of iodine per atom of olefinic hydrogen. Hence measurement can be converted to the equivalent Iodine Value. The hydrogen nmr spectrum at 360 MHz is obtained for the test material. The integral intensity, Is, of the band derived from olefinic hydrogen in the alkyl chain and the integral intensity, Im, of the band derived from terminal methyl groups in the alkyl chains are measured.
The number of olefinic hydrogens per molecule is given by:
i x 6
I„
and the Iodine Value is given by:
I„ x 127 x 100 x 6
Im x MMW
where MMW is the mean molecular weight of the test material.
Preferred fabric softening materials comprise a 1:4 parts by weight mixture of 1,2 ditallowyl oxy-3-trimethylammoniopropane chloride made according to US 4 137 180 (Lever Bros.) with its dihardened tallowy1 counterpart.
A second aspect of the invention provides an aqueous fabric softening composition comprising a fabric softening material comprising an ester-linked amine compound of formula I and/or its corresponding quaternary ammonium compound wherein the compound comprises at least one unsaturated substituent such that the material has an Iodine value of between 5 and 24.
Preferably the composition comprises from 5% to 80% by weight of fabric softening material, more preferably from 15% to 60% by weight. Compositions of the invention are obtainable by heating the material to a temperature above 40°C followed by dispersing the material into water. Preferably the materials are heated to a temperature of above 50°C and dispersed in water at elevated temperature.
The compositions of the invention preferably have a pH of more than 2.0 and less than 8.0, more preferably less than 5.0. Especially preferred are pH values in the range of from 2.5 to 4.0.
Compositions of the invention may in addition to the above ingredients also comprise other ingredients, such as non-aqueous solvents such as C1-4 alkanols and polyhydric alcohols, pH-buffering agents such as weak acids e.g. phosphoric, benzoic or citric acids, re-wetting agents, viscosity modifiers, aluminium chlorohydrate, antigelling agents, perfumes, perfume carriers, hydrocarbons, fluorescers, colourants, hydrotropes, antifoa ing agents, antiredeposition agents, enzymes, optical brightening agents, opacifiers, stabilisers such as guar gum and polyethylene glycol, anti shrinking agents, anti-wrinkle agents, silicones, soil release agents, antioxidants, anti-corrosion agents, preservatives, dyes, bleaches, bleach precursors, drape-imparting agents, antistatic agents and ironing aids.
The invention will be further illustrated by means of the following examples : Example 1
The following compositions were prepared by melting the required amounts of unsaturated compound and saturated compound, mixing and adding the premix to hot (70°C) demineralised water while stirring.
The softening performance of the monitors was tested by treating 40g of terry monitors with a 2ml dose of a 5% dispersion of the mix in 1 litre of water, line drying and assessing for softness using an expert panel and a round robin paired comparison technique.
Softening Material Iodine Value Softness Score
Arquad 2T 4:1 2T/2HT 2:1 2T/2HT 1:2 2T/2HT 1:4 2T/2HT Arquad 2HT
Figure imgf000009_0001
Higher softness scores denote softer monitors. A difference of 0.45 between scores indicates a significant difference at the 95% confidence limit.
Arquad 2T is ditallow dimethyl ammonium chloride ex Akzo Chemie.
Arquad 2HT is dihardened tallow dimethyl ammonium chloride ex Akzo Chemie.
These results show that mixing conventional quaternary ammonium compounds to iodine values of 42 does not produce a .significant increase in softening performance. Example 2
Compositions were prepared and softening assessed as described in Example 1.
Softeninσ Material Iodine"Value Softness Score
T TMAPC 4:1 T/HT 2:1 T/HT 1:2 T/HT 1:4 T/HT 1:8 T/HT HT TMAPC
Figure imgf000010_0001
A difference of 0.62 between scores indicates a significant difference at the 95% confidence limit.
T TMAPC is 1,2 ditallowyloxy-3-trimethylammoniopropane chloride ex Hoescht.
HT TMAPC is 1,2 dihardened tallowyloxy-3-trimethyl- am oniopropane chloride ex Hoescht.
These results show that mixing ester-linked quaternary ammonium compounds to give a material with an Iodine value of between 5 and 24 leads to an increase in softening performance. Example 3
5% by weight dispersions of 4:1 mixtures of hardened tallow quaternary ammonium material to soft tallow quaternary ammonium material were prepared by co-melting the materials and adding the premix to hot water (70°C) with stirring. The dispersions were cooled to room temperature with stirring. 2ml of the dispersions were added to 1 of 14°FH water containing 0.001% of alkyl benzene sulphonate to simulate anionic carry over from the main wash. Three test monitors (40-50g terry towelling) were placed in the dispersions and agitated in a tergotometer (5 mins, 60rpm) . The monitors were line dried and softening assessed using a round robin paired comparison.
Mixtures
5% Arquad 2HT
5% 4:1 Arquad 2HT:Arquad 2T 5% 4:1 Tetranyl AHT-1:AT-1 5% 4:1 HT TMAPC:T TMAPC 5% 4:1 Rewoquat W75H:W75
Figure imgf000011_0001
Rewoquat W75H is dihardened tallow imidazolinium quaternary.
Rewoquat W75 is ditallow imidazolinium quaternary.
Tetranyl AT-1 is N-methyl, N,N di(β-tallowyloxy ethyl) N β-hydroxyethyl ammonium chloride ex Kao. Tetranyl AHT-1 is N-methyl N,N di (β-hardened tallowyloxy ethyl) N β-hydroxyethyl ammonium chloride ex Kao. These results show that at the 95% significance level, mixtures of hard and soft 1,2 di-tallowyloxy-3-trimethylammonio propane chloride give better softening performance than all the other mixtures tested.

Claims

Claims
A fabric softening material comprising an ester- linked amine compound and/or its corresponding quaternary ammonium compound of general formula I.
Figure imgf000013_0001
N (CH2)n CH (CH2)m CH2COOR2 (I)
I I
R, COOR,
where each Rλ group is independently selected from C.4 alkyl, alkenyl, or hydroxyalkyl groups; each R2 group is independently selected from C8_28 or alkenyl groups and n and m are integers from 1 to 5; such that the material has an Iodine value of between 5 and 24.
2. A fabric softening material as claimed in any preceding claim wherein the material has an Iodine Value between 5 and 20.
3. A fabric softening material as claimed in claim 1 comprising at least 80% by weight of the ester-linked amine and/or its corresponding quaternary ammonium compound.
4. A fabric softening material as claimed in claim 1 additionally comprising an extender material selected from:
a. tertiary amine or quaternary ammonium compounds comprising one long alkyl or alkenyl group with more than 10 carbon atoms; b. predominantly unbranched linear nonionic materials; and
c. mixtures thereof.
5. A fabric softening material comprising 1 part by weight of oxy-3-trimethylammoniopropane chloride with 4 parts of its dihardened tallowyl counterpart.
6. An aqueous fabric softening composition comprising a fabric softening material comprising from 5 to 80% by weight of an ester-linked amine compound of general formula I.
7. An aqueous fabric softening composition as claimed in claim 6 wherein the pH lies between 2 and 8.
PCT/GB1992/001181 1991-07-05 1992-06-30 Fabric softening composition WO1993001265A1 (en)

Priority Applications (5)

Application Number Priority Date Filing Date Title
CA002112816A CA2112816C (en) 1991-07-05 1992-06-30 Fabric softening composition
EP92913677A EP0593542B1 (en) 1991-07-05 1992-06-30 Fabric softening composition
US08/170,351 US5407589A (en) 1991-07-05 1992-06-30 Fabric softening composition
JP05502058A JP3076063B2 (en) 1991-07-05 1992-06-30 Textile soft composition
DE69213016T DE69213016T2 (en) 1991-07-05 1992-06-30 LAUNDRY SOFTENER

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GB9114540.9 1991-07-05
GB919114540A GB9114540D0 (en) 1991-07-05 1991-07-05 Fabric softening composition

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WO1993001265A1 true WO1993001265A1 (en) 1993-01-21

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US (1) US5407589A (en)
EP (1) EP0593542B1 (en)
JP (1) JP3076063B2 (en)
CA (1) CA2112816C (en)
DE (1) DE69213016T2 (en)
ES (1) ES2091479T3 (en)
GB (1) GB9114540D0 (en)
WO (1) WO1993001265A1 (en)

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5476599A (en) * 1993-08-06 1995-12-19 The Procter & Gamble Company Dryer-activated fabric conditioning and antistatic compositions containing biodegradable compounds having unsaturation
US5693769A (en) * 1991-12-13 1997-12-02 Transcell Technologies, Inc. Glycosylated steroid derivatives for transport across biological membranes and process for making and using same
US5795870A (en) * 1991-12-13 1998-08-18 Trustees Of Princeton University Compositions and methods for cell transformation
EP0734433B1 (en) * 1993-12-13 2000-03-22 The Procter & Gamble Company Viscosity stable concentrated liquid fabric softener compositions
US6559117B1 (en) 1993-12-13 2003-05-06 The Procter & Gamble Company Viscosity stable concentrated liquid fabric softener compositions
WO2004027002A1 (en) * 2002-09-19 2004-04-01 Unilever Plc Fabric conditioning compositions
WO2006027055A1 (en) * 2004-09-11 2006-03-16 Unilever Plc Fabric treatment composition

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* Cited by examiner, † Cited by third party
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US5501806A (en) * 1993-07-15 1996-03-26 Colgate-Palmolive Co. Concentrated liquid fabric softening composition
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JP3076063B2 (en) 2000-08-14
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GB9114540D0 (en) 1991-08-21
DE69213016T2 (en) 1997-02-06
CA2112816A1 (en) 1993-01-21
JPH06509145A (en) 1994-10-13
EP0593542B1 (en) 1996-08-21
DE69213016D1 (en) 1996-09-26
CA2112816C (en) 2003-03-18
EP0593542A1 (en) 1994-04-27

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