WO1995022594A1 - Fabric softening composition - Google Patents

Fabric softening composition Download PDF

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Publication number
WO1995022594A1
WO1995022594A1 PCT/EP1995/000624 EP9500624W WO9522594A1 WO 1995022594 A1 WO1995022594 A1 WO 1995022594A1 EP 9500624 W EP9500624 W EP 9500624W WO 9522594 A1 WO9522594 A1 WO 9522594A1
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WO
WIPO (PCT)
Prior art keywords
fabric softening
perfume
carrier substance
softening composition
composition according
Prior art date
Application number
PCT/EP1995/000624
Other languages
French (fr)
Inventor
Stuart Bernard Fraser
John Stuart Parsons
Edwin Willis
Original Assignee
Unilever Plc
Unilever N.V.
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 N.V. filed Critical Unilever Plc
Priority to DE69505358T priority Critical patent/DE69505358T2/en
Priority to EP95911247A priority patent/EP0746603B1/en
Priority to AU18911/95A priority patent/AU698882B2/en
Priority to BR9506843A priority patent/BR9506843A/en
Publication of WO1995022594A1 publication Critical patent/WO1995022594A1/en

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Classifications

    • 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
    • C11D1/02Anionic compounds
    • C11D1/04Carboxylic acids or salts thereof
    • 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
    • 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
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/50Perfumes
    • C11D3/502Protected perfumes
    • C11D3/505Protected perfumes encapsulated or adsorbed on a carrier, e.g. zeolite or clay

Definitions

  • the present invention relates to fabric softening compositions, in particular the invention relates to aqueous dispersions of biodegradable fabric softening compositions comprising a water insoluble cationic fabric softening agent and perfume.
  • the compositions are stable on storage and exhibit excellent perfume delivery when removed from a washing machine.
  • Rinse added fabric softener compositions are well known. Typically such compositions contain a water insoluble quaternary ammonium fabric softening agent dispersed in water at a level of softening agent up to 7% by weight in which case the compositions are considered dilute, or at levels from 7% to 50% in which case the compositions are considered concentrates.
  • fabric softening compositions desirably have other benefits such as delivering perfume onto fabrics.
  • the fabric conditioning market is moving towards more concentrated compositions.
  • One of the problems associated with such fabric softening compositions is that on storage they are physically unstable. This problem is accentuated by the presence of a perfume; the greater the level of perfume the worse the stability problem becomes.
  • EP 280 550 (Unilever) it has been proposed to improve the physical stability of dilute compositions comprising biodegradable, ester-linked quaternary ammonium compounds and fatty acid by the addition of nonionic surfactants.
  • EP 507 478 (Unilever) discloses a physically stable fabric softening c mposition comprising a water insoluble, biodegradable, ester-linked quaternary ammonium compounds and a nonionic stabilising agent .
  • compositions comprising biodegradable ester-linked quaternary ammonium compounds the problem of physical instability is more acute than with traditional quaternary ammonium compounds .
  • CA 1 111 616 discloses a fabric softening composition comprising 0.1 to 10 wt% ⁇ > ⁇ a cationic fabric softener and 0.1 wt% to 20 wt % of particles.
  • the particles are comprised of a carrier substance and a perfume and have a melting point of from 38°C to 150°C, preferably from 65°C to 100°C.
  • fabric softening compositions comprising quaternary ammonium compounds may exhibit excellent perfume substantivity and good storage stability.
  • a fabric softening composition comprising: i) a quaternary ammonium fabric softening agent,
  • the slip point of the perfume/carrier substance mix is measured as defined by British Standard BS 684 section 1.3 1991 ISO 6321:1991 (UK) .
  • a further aspect of the invention is provided by a process for preparing a fabric softening composition as defined above, which comprises of the following steps:
  • a further advantage afforded by the present invention is that the degree of fabric softening may be varied to suit different customer requirements in different markets, while maintaining high perfume delivery.
  • the invention also allows perfume to be incorporated without excessive perfume intensity from the undiluted product.
  • the perfume carrier substance mix has a slip point below 37°C; preferably from 0 to 37°C. More preferably it has a slip point between 20°C and 37°C.
  • compositions of the invention are liquids, more preferably comprising an aqueous base.
  • the carrier substance is an organic material.
  • the carrier substance is a fatty ester of a mono or polyhydric alcohol having from 1 to about 24 carbon atoms in the hydrocarbon chain with the proviso that the total number of carbon atoms in the carrier substance is equal to or greater than 16 and that at least one of the hydrocarbons radicals in the ester has 12 or more carbon atoms.
  • fatty esters are preferably odourless.
  • the carrier substance in the perfume/carrier substance mix is a fatty acid glyceride or mixtures of fatty acid glycerides .
  • Especially preferred carrier substances are triglycerides, most preferred are palm oil and tallow oil.
  • the perfume/carrier substance mix is preferably present at a level of from 1 to 10% of the composition, more preferably 3 wt% to 7 wt% of the total composition.
  • the ratio of perfume to carrier substance is from 1:50 to 1:1, more preferably 1:20 to 1:2, most preferably 1:7 to 1:2.
  • the ratio of perfume/carrier substance mix to quaternary ammonium fabric softening agent is in the ratio of 5:1 to 1:10, more preferably 2:1 to 1:10.
  • the quaternary ammonium compound is biodegradable and has at least one ester link.
  • Advantageously th- ⁇ fabric softening composition comprises a water insoluble cationic compound having two C 12 . 28 alkyl or alkenyl groups connected to the N atom via one or more ester links.
  • a preferred type of ester-linked .quaternary ammonium fabric softening agent for use in the compositions according to the invention can be represented by the formula:
  • each Rj group is independently selected from C ⁇ alkyl, or hydroxyalkyl or C__ 4 alkyl groups; and wherein each R 2 group is independently selected from C s _- ⁇ alkyl or alkenyl groups;
  • T is -C-O- or -C-0-; and n is an integer from 0-5.
  • a second preferred type of quaternary ammonium fabric softening agent can be represented by the formula:
  • R 1# n and R 2 are as defined above.
  • Preferred materials of this class- and their method of preparation are, for example, described in US 4 137 180 (Lever Brothers) .
  • Preferably these materials comprise small amounts of the corresponding monoester as described in US 4 137 180, for example 1-tallowoxy, 2-hydroxytrimethyl ammonium propane chloride.
  • the level of ester linked quaternary ammonium compounds is at least 1% by weight of the composition, more preferably more than 7% by weight of the composition; especially interesting are concentrated compositions which comprise between 10 and 30 % by weight of ester-linked quaternary ammonium compound.
  • compositions of the invention may also contain nonionic stabilisers.
  • Suitable non. c stabilisers which can be used include the condensation products of C-, - C 22 primary linear alcohols with 10 to 25 moles of ethylene oxide. Use of less than 10 moles of ethylene oxide, especially when the alkyl chain is in the tallow range, leads to unacceptably high aquatic toxicity.
  • nonionic stabilisers are preferred: Genapol T-110, Genapol T-150, Genapol T-200, Genapol C-200 all ex Hoechst AG, Lutensol AT18 ex BASF, Genapol C-100 and Genapol C-150 ex Hoechst, or fatty alcohols for example Laurex CS, ex Albright and Wilson or Adol 340 ex Sherex (all Trade Marks) .
  • the nonionic stabiliser has an HLB value of from 10 to 20, more preferably 12 to 20.
  • the level of nonionic stabiliser is within the range of from 0.1 to 10% by weight, more preferably from 0.5 to 5% by weight, most preferably from 1 to 4% by weight.
  • the composition can also contain fatty acids, for example C e - C 24 alkyl or alkenyl monocarboxylic acids, or polymeric carboxylic acids.
  • fatty acids for example C e - C 24 alkyl or alkenyl monocarboxylic acids, or polymeric carboxylic acids.
  • saturated fatty acids are used, in particular, hardened tallow C 16 -C ⁇ e fatty acids.
  • the level of fatty acid material is preferably more than 0.1% by weight, more preferably more than 0.2% by weight. Especially preferred are concentrates comprising from 0.5 to 20% by weight of fatty acid, more preferably 1% to 10% by weight.
  • the weight ratio of quaternary ammonium material to fatty acid material is preferably from 10:1 to 1:10.
  • compositions of the invention preferably have a pH of more than 1.5, more preferably less than 5.
  • the composition can also contain one or more optional ingredients, selected from non-aqueous solvents, pH buffering agents, perfumes, perfume carriers, fluorescers, colorants, hydrotropes, antifoaming agents, antiredeposition agents, enzymes, optical brightening agents, opacifiers, anti- shrinking agents, anti-wrinkle agents, anti-spotting agents, germicides, fungicides, anti-oxidants, anti-corrosion agents, drape imparting agents, antistatic agents and ironing aids.
  • optional ingredients selected from non-aqueous solvents, pH buffering agents, perfumes, perfume carriers, fluorescers, colorants, hydrotropes, antifoaming agents, antiredeposition agents, enzymes, optical brightening agents, opacifiers, anti- shrinking agents, anti-wrinkle agents, anti-spotting agents, germicides, fungicides, anti-oxidants, anti-corrosion agents, drape imparting agents, antistatic agents and ironing aids.
  • composition may also contain nonionic fabric softening agents.
  • compositions were prepared by the following method: antifoam, preservative and dyestuff were dissolved in warm (40°C) water followed by addition of electrolyte (citric or CaCl 2 )to form an aqueous solution.
  • Nonionic (Coco 20) 1.0 1.0 3.0 3.0
  • Examples A and B went solid within 3 days at 37°C storage.
  • Examples 1 and 2 showed viscosities as follows:
  • composition 4 300g of an unperfumed base (at 35 cP) of composition 4 was prepared with either perfume alone or perfume/palm oil mix by milling into the base using a Silverson mixer over a 5 min period. The samples were left at ambient temperature.
  • Examples were prepared by dispersing the cationic fabric softening agent in water, followed by the addition of the perfume or perfume/carrier substance mix.
  • the perfume substantivity was tested by adding lg of the resulting composition to 1 litre of water at ambient temperature and agitating for 2 minutes to disperse. Four 19 x 19 squares of terry towelling were than immersed in the dispersion and left for 5 minutes. The terry towelling was then removed from the dispersion, n i dry and line dried overnight .
  • the terry towelling samples were evaluated by a panel of people using a random design to measure perfume strength. Each treatment was evaluated six times The data was analysed by analysis of variance.
  • a score of 0 indicates a no perfume impact
  • a score of 5 indicates a very strong perfume impact

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  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Wood Science & Technology (AREA)
  • Organic Chemistry (AREA)
  • Dispersion Chemistry (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
  • Detergent Compositions (AREA)
  • Cosmetics (AREA)

Abstract

A fabric softening composition with good storage stability and excellent perfume stability is disclosed. The composition contains a cationic softening agent and a perfume/carrier substance with a slip point below 45 °C. Preferred carrier substances are tallow oil and palm oil.

Description

FABRIC SOFTENING COMPOSITION
The present invention relates to fabric softening compositions, in particular the invention relates to aqueous dispersions of biodegradable fabric softening compositions comprising a water insoluble cationic fabric softening agent and perfume. The compositions are stable on storage and exhibit excellent perfume delivery when removed from a washing machine.
Rinse added fabric softener compositions are well known. Typically such compositions contain a water insoluble quaternary ammonium fabric softening agent dispersed in water at a level of softening agent up to 7% by weight in which case the compositions are considered dilute, or at levels from 7% to 50% in which case the compositions are considered concentrates. In addition to softening, fabric softening compositions desirably have other benefits such as delivering perfume onto fabrics.
The fabric conditioning market is moving towards more concentrated compositions. One of the problems associated with such fabric softening compositions is that on storage they are physically unstable. This problem is accentuated by the presence of a perfume; the greater the level of perfume the worse the stability problem becomes.
Physical instability manifests itself as a irreversible thickening on storage of the composition to a level where the composition is no longer pourable and can even lead to the formation of a gel. The thickening is very undesirable since the composition can no longer conveniently be used. In the past physical stability of rinse added fabric softener compositions has been improved by the addition of viscosity control agents or anti-gelling agents. For example in EP 13 780 (Procter and Gamble) viscosity control agents are added to certain concentrated compositions. The agents may include C10-C18 fatty alcohols. More recently in EP 280 550 (Unilever) it has been proposed to improve the physical stability of dilute compositions comprising biodegradable, ester-linked quaternary ammonium compounds and fatty acid by the addition of nonionic surfactants. EP 507 478 (Unilever) discloses a physically stable fabric softening c mposition comprising a water insoluble, biodegradable, ester-linked quaternary ammonium compounds and a nonionic stabilising agent .
With concentrated compositions comprising biodegradable ester-linked quaternary ammonium compounds the problem of physical instability is more acute than with traditional quaternary ammonium compounds .
CA 1 111 616 (Procter and Gamble) discloses a fabric softening composition comprising 0.1 to 10 wt% →>ϊ a cationic fabric softener and 0.1 wt% to 20 wt % of particles. The particles are comprised of a carrier substance and a perfume and have a melting point of from 38°C to 150°C, preferably from 65°C to 100°C.
We have now found that fabric softening compositions comprising quaternary ammonium compounds may exhibit excellent perfume substantivity and good storage stability.
Thus, according to one aspect of the invention there is provided a fabric softening composition a fabric softening composition comprising: i) a quaternary ammonium fabric softening agent,
ii) from 0.1 wt% to 10 wt% of a perfume/carrier substance mix having a slip point below 45°C.
The slip point of the perfume/carrier substance mix is measured as defined by British Standard BS 684 section 1.3 1991 ISO 6321:1991 (UK) .
A further aspect of the invention is provided by a process for preparing a fabric softening composition as defined above, which comprises of the following steps:
i) forming an aqueous dispersion of the quaternary ammonium fabric softening agent; ii) adding the perf me/carrier substance mix to the resulting dispersion.
One advantage of such a process is that it is simple. A further advantage afforded by the present invention is that the degree of fabric softening may be varied to suit different customer requirements in different markets, while maintaining high perfume delivery.
The invention also allows perfume to be incorporated without excessive perfume intensity from the undiluted product.
To give excellent perfume delivery when laundry is removed from the washing machine it is advantageous if the perfume carrier substance mix has a slip point below 37°C; preferably from 0 to 37°C. More preferably it has a slip point between 20°C and 37°C.
Preferably the compositions of the invention are liquids, more preferably comprising an aqueous base. It is preferred if the carrier substance is an organic material. It is further preferred if the carrier substance is a fatty ester of a mono or polyhydric alcohol having from 1 to about 24 carbon atoms in the hydrocarbon chain with the proviso that the total number of carbon atoms in the carrier substance is equal to or greater than 16 and that at least one of the hydrocarbons radicals in the ester has 12 or more carbon atoms. Such fatty esters are preferably odourless.
It is preferred if the carrier substance in the perfume/carrier substance mix is a fatty acid glyceride or mixtures of fatty acid glycerides . Especially preferred carrier substances are triglycerides, most preferred are palm oil and tallow oil.
The perfume/carrier substance mix is preferably present at a level of from 1 to 10% of the composition, more preferably 3 wt% to 7 wt% of the total composition.
For good perfume delivery it is advantageous if the ratio of perfume to carrier substance is from 1:50 to 1:1, more preferably 1:20 to 1:2, most preferably 1:7 to 1:2.
To achieve good perfume delivery from the product it is favourable if the ratio of perfume/carrier substance mix to quaternary ammonium fabric softening agent is in the ratio of 5:1 to 1:10, more preferably 2:1 to 1:10.
It is preferable if the quaternary ammonium compound is biodegradable and has at least one ester link.
Advantageously th-^ fabric softening composition comprises a water insoluble cationic compound having two C12.28 alkyl or alkenyl groups connected to the N atom via one or more ester links. A preferred type of ester-linked .quaternary ammonium fabric softening agent for use in the compositions according to the invention can be represented by the formula:
Figure imgf000007_0001
Figure imgf000007_0002
Figure imgf000007_0003
wherein each Rj group is independently selected from C^ alkyl, or hydroxyalkyl or C__4 alkyl groups; and wherein each R2 group is independently selected from Cs_-ε alkyl or alkenyl groups;
O O
T is -C-O- or -C-0-; and n is an integer from 0-5.
A second preferred type of quaternary ammonium fabric softening agent can be represented by the formula:
O
OCR- I
(R1)3N+- (CH2)n CH
CH.OCR-
O
wherein R1# n and R2 are as defined above. Preferred materials of this class- and their method of preparation are, for example, described in US 4 137 180 (Lever Brothers) . Preferably these materials comprise small amounts of the corresponding monoester as described in US 4 137 180, for example 1-tallowoxy, 2-hydroxytrimethyl ammonium propane chloride.
Preferably the level of ester linked quaternary ammonium compounds is at least 1% by weight of the composition, more preferably more than 7% by weight of the composition; especially interesting are concentrated compositions which comprise between 10 and 30 % by weight of ester-linked quaternary ammonium compound.
Compositions of the invention may also contain nonionic stabilisers. Suitable non. c stabilisers which can be used include the condensation products of C-, - C22 primary linear alcohols with 10 to 25 moles of ethylene oxide. Use of less than 10 moles of ethylene oxide, especially when the alkyl chain is in the tallow range, leads to unacceptably high aquatic toxicity. In particular the following nonionic stabilisers are preferred: Genapol T-110, Genapol T-150, Genapol T-200, Genapol C-200 all ex Hoechst AG, Lutensol AT18 ex BASF, Genapol C-100 and Genapol C-150 ex Hoechst, or fatty alcohols for example Laurex CS, ex Albright and Wilson or Adol 340 ex Sherex (all Trade Marks) . Preferably the nonionic stabiliser has an HLB value of from 10 to 20, more preferably 12 to 20. Preferably, the level of nonionic stabiliser is within the range of from 0.1 to 10% by weight, more preferably from 0.5 to 5% by weight, most preferably from 1 to 4% by weight.
The composition can also contain fatty acids, for example Ce - C24 alkyl or alkenyl monocarboxylic acids, or polymeric carboxylic acids. Preferably saturated fatty acids are used, in particular, hardened tallow C16-Cιe fatty acids.
The level of fatty acid material is preferably more than 0.1% by weight, more preferably more than 0.2% by weight. Especially preferred are concentrates comprising from 0.5 to 20% by weight of fatty acid, more preferably 1% to 10% by weight. The weight ratio of quaternary ammonium material to fatty acid material is preferably from 10:1 to 1:10.
The compositions of the invention preferably have a pH of more than 1.5, more preferably less than 5.
The composition can also contain one or more optional ingredients, selected from non-aqueous solvents, pH buffering agents, perfumes, perfume carriers, fluorescers, colorants, hydrotropes, antifoaming agents, antiredeposition agents, enzymes, optical brightening agents, opacifiers, anti- shrinking agents, anti-wrinkle agents, anti-spotting agents, germicides, fungicides, anti-oxidants, anti-corrosion agents, drape imparting agents, antistatic agents and ironing aids.
The composition may also contain nonionic fabric softening agents.
The invention will now be illustrated by the following non- limiting examples. In the examples all percentages are expressed by weight.
Comparative Examples are designated by letters, while Examples of the invention are designated by numbers. Examples 1, 2, 3, 4, A, B, C and D
Compositions were prepared by the following method: antifoam, preservative and dyestuff were dissolved in warm (40°C) water followed by addition of electrolyte (citric or CaCl2)to form an aqueous solution. The biodegradable cationic fabric softening agent (HT TMAPC = 1-trimethyl ammonium-2,3 dihardened tallowoyloxy propane chloride with some tallow fatty acid impurities (6:1 ratio) ex Hoechst) was melted (75-80°C) and mixed with the nonionic (coco ethoxylate 20EO:coco 20) . This premix was added to the aqueous solution over 5 in with stirring. The resulting mixture was recirculated through a Janke and Kunkel mill set at max shear (10,000 rpm) . This recirculation/shearing continued for 30 mins after premix addition. Perfume was stirred directly into the mix _r a premixed with palm/tallow oil at a temperature of 40-45°C and then added by milling into the product over a 10 min period at 8000 rpm.
(The palm/tallow raw materials are refined, bleached and deodorised) .
TABLE 1
Formulations EXAMPLES
A 1 B 2
Citric Acid 3.5 3.5 3.5 3.5
HT TMAPC 20 20 20 20
Nonionic (Coco 20) 1.0 1.0 3.0 3.0
An ifoam 0.06 0.06 0.06 0.06
Preservative 0.02 0.02 0.02 0.02
Perfume 1.0 1.0 1.0 1.0
Palm Oil - 3.0 - -
Tallow Oil - - - 3.0
De in Water to 100 to 100 to 100 to 100
TABLE 2
Example C 3 D 4
CaCl2 0.20 0.20 0.20 0.20
HT TMAPC 20 20 20 20
Nonionic (Coco 20) 3.0 3.0 3.0 3.0
An ifoam 0.06 0.06 0.06 0.06
Preservative 0.02 0.02 0.02 0.02
Perfume 1.0 1.0 1.0 1.0
Palm Oil - 3.0 - -
Tallow Oil - - - 5.0
Demin Water to 100 to 100 to 100 to 100 Viscosity measurements were taken at 25° and at 106 sec"1, shear rate using a Haake VT501 rotoviscometer.
Examples A and B went solid within 3 days at 37°C storage. Examples 1 and 2 showed viscosities as follows:
TABLE 3
Time @ 37°C Viscosity
1 2
Initial 69 cP 118 cP
10 days - 122 cP
" days 65 cP -
22 days - 125 CP
28 days 93 cP -
29 days - 121 cP
38 days - 118 CP
( 6 days - 129 cP
Examples C and D went solid within 3hrs at ambient temperature.
Examples 3 and 4 showed viscosities as follows: TABLE 4
Time & 37°C Vise
3 4
Initial 64 cP 38 CP
7 days - 34 cP
10 days 68 cP -
19 days - 33 cP
21 days 82 cP -
43 days - 36 cP
56 days 87 cP -
58 days - 39 cP
71 days 99 cP -
Examples 5.6.7.8.E.F.G and H
To demonstrate that this invention works with a variety of perfumes, 300g of an unperfumed base (at 35 cP) of composition 4 was prepared with either perfume alone or perfume/palm oil mix by milling into the base using a Silverson mixer over a 5 min period. The samples were left at ambient temperature.
TABLE 5
Examples Perfume Palm Oil Time to go Solid
E Perfume A - 10 mins
5 Perfume A 3% Liquid after 10 days
F Perfume B - 2-3 days
6 Perfume B 3% Liquid after 10 days
G Perfume C - 10 mins
7 Perfume C 3% Liquid after 10 days
H Perfume D - 1-2 days
8 Perfume D 3% Liquid after 10 days
Examples 9,10 and I
Examples were prepared by dispersing the cationic fabric softening agent in water, followed by the addition of the perfume or perfume/carrier substance mix.
The perfume substantivity was tested by adding lg of the resulting composition to 1 litre of water at ambient temperature and agitating for 2 minutes to disperse. Four 19 x 19 squares of terry towelling were than immersed in the dispersion and left for 5 minutes. The terry towelling was then removed from the dispersion, n i dry and line dried overnight .
The terry towelling samples were evaluated by a panel of people using a random design to measure perfume strength. Each treatment was evaluated six times The data was analysed by analysis of variance.
TABLE 6
Example 9 10 I
HT TMAPC 14.5 14.5 14.5
Perfume 0.9 0.9 0.9 Softline 2000
Palm oil 5.0 2.7 -
Water t- r. i nn
The perfume release on the terry towelling was as illustrated in the table below:
TABLE 7
Example
9 10 I
Perfume Impact 1.5 1.7 0.5
A score of 0 indicates a no perfume impact
A score of 5 indicates a very strong perfume impact

Claims

Claims
1) A fabric softening composition comprising:
i) a quaternary ammonium fabric softening agent and; ii) from 0.1 wt% to 10 wt% of a perfume/carrier substance mix having a slip point below 45°C.
2) A fabric softening composition according to claim 1 in which the perfume/carrier substance mix has a slip point below 37°C.
3) A fabric softening composition according to claim 2 in which the perfume/carrier substance mix has a slip point from 0°C to 37°C.
4) A fabric softening composition according to any preceding claim in which the carrier substance in the perfume/carrier substance mix is a fatty acid glyceride or mixtures of fatty acid glycerides.
5) A fabric softening composition according to claim 4 in which the carrier substance in the perfume/carrier substance mix is palm oil.
6) A fabric softening composition according to claim 4 in which the carrier substance in the perfume/carrier substance mix is tallow oil.
7) A fabric softening composition according to any preceding claim in which the perfume/carrier substance mix is present at a level from 3wt% to 7wt% of the total composition. 8) A fabric softening composition according to any preceding claim in which the ratio of perfume to carrier substance is from 1:7 to 1:2.
9) A fabric softening composition according to any preceding claim in which the quaternary ammonium fabric softening agent is a biodegradable quaternary ammonium material with at least one ester link.
10) A fabric softening composition according to claim 9 in which the biodegradable quaternary ammonium material has the formula:
O
OCR2 I
(R^s-NT- (CH,)n CH
CH.OCR-
O
wherein each Rj group is independently selected from C1-4 alkyl, hydroxyalkyl groups or C2-4 alkenyl groups; and wherein each R2 group is independently selected from C8_ alkyl or alkenyl groups;
11) A fabric softening composition according to any preceding claim which is liquid.
12) A process for preparing a fabric softening composition according to claim 1, which comprises of the following steps: i) forming an aqueous dispersion of the quaternary ammonium fabric softening agent;
iii) adding the perfume/carrier substance mix to the resulting dispersion.
PCT/EP1995/000624 1994-02-21 1995-02-17 Fabric softening composition WO1995022594A1 (en)

Priority Applications (4)

Application Number Priority Date Filing Date Title
DE69505358T DE69505358T2 (en) 1994-02-21 1995-02-17 TISSUE SOFTENER COMPOSITION
EP95911247A EP0746603B1 (en) 1994-02-21 1995-02-17 Fabric softening composition
AU18911/95A AU698882B2 (en) 1994-02-21 1995-02-17 Fabric softening composition
BR9506843A BR9506843A (en) 1994-02-21 1995-02-17 Fabric softening composition

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GB9403242.2 1994-02-21
GB9403242A GB9403242D0 (en) 1994-02-21 1994-02-21 Fabric softening composition

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AU (1) AU698882B2 (en)
BR (1) BR9506843A (en)
DE (2) DE69532508T2 (en)
ES (2) ES2123962T3 (en)
GB (1) GB9403242D0 (en)
WO (1) WO1995022594A1 (en)
ZA (1) ZA951428B (en)

Cited By (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1996012785A1 (en) * 1994-10-20 1996-05-02 The Procter & Gamble Company Fabric softener compositions with reduced environmental impact
WO1997016516A1 (en) * 1995-11-03 1997-05-09 The Procter & Gamble Company Stable high perfume, low active fabric softener compositions
WO1997031086A1 (en) * 1996-02-26 1997-08-28 The Procter & Gamble Company Fabric softener composition with improved environmental impact
WO1997034976A1 (en) * 1996-03-22 1997-09-25 The Procter & Gamble Company Concentrated, stable, premix for forming fabric softening composition
EP0829531A1 (en) * 1996-08-22 1998-03-18 Unilever Plc Fabric conditioning composition
EP0845523A2 (en) * 1996-11-28 1998-06-03 Givaudan-Roure (International) S.A. Ingredient preventing the viscosity problem encountered in a perfumed concentrated fabric softener
US6022845A (en) * 1995-11-03 2000-02-08 The Procter & Gamble Co. Stable high perfume, low active fabric softener compositions
WO2002004587A1 (en) * 2000-07-07 2002-01-17 Givaudan S.A. Process for imparting conditioning and good fragrance perception to both damp and dry fabric
WO2002033032A2 (en) * 2000-10-17 2002-04-25 Unilever Plc Fabric conditioning compositions
EP1279726A1 (en) * 2001-07-27 2003-01-29 Givaudan SA Fabric softener composition
WO2003055968A1 (en) * 2002-01-04 2003-07-10 Unilever Plc Fabric conditioning compositions
WO2003082356A2 (en) * 2002-04-03 2003-10-09 Dow Corning Corporation Fragrance containing emulsions
WO2006007911A1 (en) * 2004-07-20 2006-01-26 Unilever Plc Laundry product
US7691801B2 (en) 2006-05-31 2010-04-06 The Sun Products Corporation Laundry product
US7763579B2 (en) 2004-10-29 2010-07-27 The Sun Products Corporation Method of preparing a laundry product

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB0014891D0 (en) 2000-06-16 2000-08-09 Unilever Plc Fabric softening compositions

Citations (5)

* Cited by examiner, † Cited by third party
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FR2369340A1 (en) * 1976-10-29 1978-05-26 Procter & Gamble PERFUMED COMPOSITION USABLE FOR PACKAGING FABRICS
EP0005618A1 (en) * 1978-05-16 1979-11-28 Unilever Plc Deodorant products, preparation and use thereof
EP0239910A2 (en) * 1986-04-02 1987-10-07 The Procter & Gamble Company Biodegradable fabric softeners
WO1991013143A1 (en) * 1990-02-20 1991-09-05 The Procter & Gamble Company Coated perfume particles
WO1993005137A1 (en) * 1991-08-28 1993-03-18 The Procter & Gamble Company Liquid fabric softener with protected cyclodextrine/perfume complex

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2369340A1 (en) * 1976-10-29 1978-05-26 Procter & Gamble PERFUMED COMPOSITION USABLE FOR PACKAGING FABRICS
EP0005618A1 (en) * 1978-05-16 1979-11-28 Unilever Plc Deodorant products, preparation and use thereof
EP0239910A2 (en) * 1986-04-02 1987-10-07 The Procter & Gamble Company Biodegradable fabric softeners
WO1991013143A1 (en) * 1990-02-20 1991-09-05 The Procter & Gamble Company Coated perfume particles
WO1993005137A1 (en) * 1991-08-28 1993-03-18 The Procter & Gamble Company Liquid fabric softener with protected cyclodextrine/perfume complex

Cited By (22)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1996012785A1 (en) * 1994-10-20 1996-05-02 The Procter & Gamble Company Fabric softener compositions with reduced environmental impact
WO1997016516A1 (en) * 1995-11-03 1997-05-09 The Procter & Gamble Company Stable high perfume, low active fabric softener compositions
US6022845A (en) * 1995-11-03 2000-02-08 The Procter & Gamble Co. Stable high perfume, low active fabric softener compositions
WO1997031086A1 (en) * 1996-02-26 1997-08-28 The Procter & Gamble Company Fabric softener composition with improved environmental impact
WO1997034976A1 (en) * 1996-03-22 1997-09-25 The Procter & Gamble Company Concentrated, stable, premix for forming fabric softening composition
EP0829531A1 (en) * 1996-08-22 1998-03-18 Unilever Plc Fabric conditioning composition
EP0845523A2 (en) * 1996-11-28 1998-06-03 Givaudan-Roure (International) S.A. Ingredient preventing the viscosity problem encountered in a perfumed concentrated fabric softener
EP0845523A3 (en) * 1996-11-28 1999-01-27 Givaudan-Roure (International) S.A. Ingredient preventing the viscosity problem encountered in a perfumed concentrated fabric softener
WO2002004587A1 (en) * 2000-07-07 2002-01-17 Givaudan S.A. Process for imparting conditioning and good fragrance perception to both damp and dry fabric
WO2002033032A3 (en) * 2000-10-17 2002-06-20 Unilever Plc Fabric conditioning compositions
WO2002033032A2 (en) * 2000-10-17 2002-04-25 Unilever Plc Fabric conditioning compositions
EP1279726A1 (en) * 2001-07-27 2003-01-29 Givaudan SA Fabric softener composition
WO2003012022A1 (en) * 2001-07-27 2003-02-13 Givaudan Sa Fabric softener composition
WO2003055968A1 (en) * 2002-01-04 2003-07-10 Unilever Plc Fabric conditioning compositions
US6894011B2 (en) 2002-01-04 2005-05-17 Unilever Home & Personal Care Usa, A Division Of Conopco, Inc. Fabric conditioning compositions
WO2003082356A2 (en) * 2002-04-03 2003-10-09 Dow Corning Corporation Fragrance containing emulsions
WO2003082356A3 (en) * 2002-04-03 2003-11-20 Dow Corning Fragrance containing emulsions
WO2006007911A1 (en) * 2004-07-20 2006-01-26 Unilever Plc Laundry product
US7718596B2 (en) 2004-07-20 2010-05-18 The Sun Products Corporation Unit dose laundry products containing fatty acid esters
EP1773973B1 (en) 2004-07-20 2016-01-13 Unilever PLC Laundry product
US7763579B2 (en) 2004-10-29 2010-07-27 The Sun Products Corporation Method of preparing a laundry product
US7691801B2 (en) 2006-05-31 2010-04-06 The Sun Products Corporation Laundry product

Also Published As

Publication number Publication date
EP0787793A2 (en) 1997-08-06
EP0746603A1 (en) 1996-12-11
DE69532508D1 (en) 2004-03-04
DE69532508T2 (en) 2004-07-08
EP0746603B1 (en) 1998-10-14
AU698882B2 (en) 1998-11-12
AU1891195A (en) 1995-09-04
ZA951428B (en) 1996-08-21
EP0787793A3 (en) 1998-08-12
ES2212008T3 (en) 2004-07-16
DE69505358T2 (en) 1999-03-25
EP0787793B1 (en) 2004-01-28
ES2123962T3 (en) 1999-01-16
BR9506843A (en) 1997-10-14
DE69505358D1 (en) 1998-11-19
GB9403242D0 (en) 1994-04-13

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