EP1969107A1 - Clear fabric conditioner composition - Google Patents
Clear fabric conditioner compositionInfo
- Publication number
- EP1969107A1 EP1969107A1 EP06829617A EP06829617A EP1969107A1 EP 1969107 A1 EP1969107 A1 EP 1969107A1 EP 06829617 A EP06829617 A EP 06829617A EP 06829617 A EP06829617 A EP 06829617A EP 1969107 A1 EP1969107 A1 EP 1969107A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- fabric conditioner
- weight
- composition
- clear
- quaternary ammonium
- Prior art date
- Legal status (The legal status 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 status listed.)
- Ceased
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/38—Cationic compounds
- C11D1/62—Quaternary ammonium compounds
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/66—Non-ionic compounds
- C11D1/835—Mixtures of non-ionic with cationic compounds
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/20—Organic compounds containing oxygen
- C11D3/2003—Alcohols; Phenols
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/50—Perfumes
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/66—Non-ionic compounds
- C11D1/72—Ethers of polyoxyalkylene glycols
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/20—Organic compounds containing oxygen
- C11D3/2003—Alcohols; Phenols
- C11D3/2041—Dihydric alcohols
- C11D3/2044—Dihydric alcohols linear
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/20—Organic compounds containing oxygen
- C11D3/2003—Alcohols; Phenols
- C11D3/2065—Polyhydric alcohols
Definitions
- This invention relates to clear or translucent fabric conditioner composition.
- the composition of the present invention has reduced amount of non-aqueous solvent.
- Fabric conditioners are well known in the art. Fabric conditioners that are clear or translucent have a better visual appeal and are being increasingly preferred by consumers. Consequently, various approaches have been used in the prior art to produce clear or translucent fabric conditioners .
- GB2211510 (Colgate-Palmolive Company, 1989) teaches fabric conditioning and antistatic detergent compositions or softergents which include 10-35% by weight a narrow range ethoxylate nonionic detergent, 2- 15% by weight a fabric conditioning and antistatic cationic compound such as Ci 2 -Ci 8 quaternary ammonium halide and 30-70% by weight water.
- the compositions of this prior art invention are superior in detersive action compared to identical compositions except for replacement of the narrow range ethoxylate with a broad range ethoxylate nonionic detergent .
- the superior detersive action is attributed to the presence of the narrow range ethoxylated nonionic detergent that are believed to counteract the negative effect of quaternary ammonium halide on detergency.
- This invention of is directed at improving detergency of fabric conditioner compositions .
- US005399272 (Procter & Gamble Company, 1995) teaches fabric conditioning compositions comprising 20-80% by weight of fabric conditioner active, 2-25% C 8 -C 2 2 monoalkyl cationic quaternary ammonium compound dispersibility aid and 17-75% non-aqueous solvent, wherein the fatty acyl components of the fabric conditioner active have an average Iodine Value of at least 50.
- the use of C 8 -C 22 quaternary ammonium compounds has been taught as an auxiliary ingredient to the fabric conditioner active as a dispersibility aid.
- EP1149891 (Goldschmidt Chemical Company, 2001) teaches aqueous laundry detergent compositions comprising a blend of quaternary ammonium fabric conditioner actives 1-50% by weight of at least one anionic scavenger and 50-99% by weight of at least on triglyceride based ester quat .
- the use of C 8 -C 22 quaternary ammonium compounds has been taught as an auxiliary ingredient to the fabric conditioner active as an anionic scavenger.
- one of the objects of the present invention is to devise clear or translucent fabric conditioner composition comprising fragrance which is based on less expensive fabric conditioner actives .
- Another object of the present invention is to devise clear or translucent fabric conditioner composition that has reduced level of non-aqueous solvents, preferably below 10% by weight.
- a quaternary ammonium fabric conditioner active of the formula RR 1 R 2 R 3 N + X " , where, R is an alkyl group with 16 to 22 carbon atoms, R 1 , R 2 and R 3 are alkyl groups with 1 to 4 carbon atoms, X is a an anion selected from chloride, bromide, acetate, sulfate, nitrate, and phosphate;
- a hydrotrope selected from fatty alcohol ethoxylates and alkylene polyols or mixtures thereof;
- fragrance 0.001-10% by weight fragrance
- nonaqueous solvents including short chain C 1 -C 6 alcohols, Ci-C 4 alkylene carbonates and short chain C 2 -C 8 alkyl ethers are at levels not greater than 10% by weight of the composition.
- the present invention is directed to a clear or translucent fabric conditioner composition
- a clear or translucent fabric conditioner composition comprising quaternary ammonium fabric conditioner active, hydrotrope, fragrance and water.
- the composition of the present invention is visually clear.
- a composition is termed as clear or translucent when the light transmittance at 600 nm is greater than 80%.
- the composition of the present invention preferably has a viscosity between 20-200 cP at a shear rate of 106 s "1 .
- the composition of the present invention comprises of quaternary ammonium fabric conditioner active, preferably 0.1-30%, more preferably 3-22% by weight.
- the quaternary ammonium fabric conditioner active of the present invention is of the general formula RR 1 R 2 R 3 N + X " , where R is an alkyl group with 16 to 22 carbon atoms, R 1 , R 2 and R 3 are alkyl groups with 1 to 4 carbon atoms, and X is a an anion selected from chloride, bromide, acetate, sulfate, nitrate, and phosphate.
- composition comprising at least two quaternary ammonium fabric conditioner actives wherein number of carbon atoms in R group of the actives is different.
- Preferred quaternary ammonium fabric conditioner actives are the mono long-chain alkyl quaternary fabric conditioner actives where R 1 , R 2 and R 3 each are methyl groups and R is an alkyl group with 16 to 22 carbon atoms.
- the anion of the quaternary fabric conditioner actives is selected from chloride, bromide, acetate, sulfate, nitrate, and phosphate. Chloride salt of quaternary ammonium fabric conditioner actives is particularly preferred.
- the most preferred quaternary ammonium fabric conditioner actives of the present invention are cetyl trimethyl ammonium chloride, stearyl trimethyl ammonium chloride and behenyl trimethyl ammonium chloride .
- the active when R is alkyl group having 16 carbon atoms, the active is present in an amount in the range of 0.5 to 10% by weight of the composition, when R is alkyl group having 18 carbon atoms, the active is present in an amount in the range of 1 to 20% by weight of the composition, and when R is alkyl group with 22 carbon atoms, the active is present in an amount in the range of 0.1 to 10% by weight of the composition.
- the inventive composition is substantially free of other conventional cationic fabric conditioner actives such as triglyceride-based ester quaternary ammonium compounds, ester quaternary ammonium compounds, and saturated or unsaturated ditallow dimethyl quaternary ammonium compounds .
- composition of the present invention preferably comprises 0.1-15 % by weight hydrotrope selected from fatty alcohol ethoxylates and alkylene polyols or mixtures thereof .
- Preferred fatty alcohol ethoxylates of the present invention are Ci 2 -Ci 8 alcohol ethoxylate having 1-20 oxyethylene units on an average.
- Alkylene polyols of the present invention are preferably C 2 -C 10 polyhydric alcohols, more preferably C 2 -C 6 alkylene glycols.
- Some examples of the polyhydric alcohols of the present invention include ethylene glycol, glycerol and hexylene glycol .
- fragrance for the purpose of this invention, means a mixture of odoriferous components, optionally mixed with a suitable solvent diluent or carrier, which is employed to impart a desired odor.
- Fragrance components and mixtures thereof may be obtained from natural products such as essential oils, absolutes, resinoids, resins and concretes, as well as synthetic products such as hydrocarbons, alcohols, aldehydes, ketones, ethers, carboxylic acids, esters, acetals, ketals, lactones, sulphides, halides, oximes, nitriles and the like, including saturated and unsaturated compounds, aliphatic, aromatic and heterocyclic compounds.
- fragrance ingredients which may be employed in the present invention are selected from one or more of; 2-Methoxy naphthalene, Allyl cyclohexylpropionate, citronellal, alpha-Ionone, alpha- Santalol, alpha- Terpineol, Ambrettolide, Amyl benzoate, Amyl cinnamate, Amyl cinnamic aldehyde, Aurantiol, Benzaldehyde, Benzophenone, Benzyl acetate, Benzyl salicylate, Beta- caryophyllene, Beta-Methyl naphthyl ketone, Cadinene, Cavacrol, Cedrol , Cedryl acetate, Cedryl formate, 2 Cinnamyl cinnamate, cis-Jasmone, Coumarin, Cyclamen aldehyde, Cyclohexyl salicylate, d-Limonene, delta- Nonalactone
- fragrance ingredients are cyclic and acyclic terpenes and terpenoids. These materials are based upon isoprene repeating units. Examples include alpha and beta pinene, myrcene, geranyl alcohol and acetate, camphene, 10 dl-limonene, alpha and beta phellandrene, tricyclene, terpinolene, allocimmane, geraniol, nerol, linanool, dihydrolinanool, citral, ionone, methyl ionone, citronellol, citronella!, alpha terpineol, beta terpineol, alpha fenchol, borneol, isoborneol, camphor, terpinen-1-ol , terpin-4-ol, 15 dihydroterpineol , methyl chavicol, anethole, 1, 4 and 1, 8 cineole, geranyl ,
- Suitable solvents, diluents or carriers for fragrance ingredients as mentioned above are for example ethanol, isopropanol, diethylene glycol monoethyl ether, dipropyl glycol and triethyl citrate.
- the composition of present invention preferably comprises 0.001-10% by weight, more preferably 1-5% by weight of fragrance.
- the fabric conditioner composition preferably comprises 45-99%, more preferably 75-90% water by weight.
- nonaqueous organic solvents are not greater than 10% by weight of the composition.
- Nonaqueous organic solvents include short chain Ci-C 6 alcohols, Ci-C 4 alkylene carbonates and short chain C 2 -C 8 alkyl ethers.
- Co-conditioners can be optionally used together with the cationic conditioning actives of the present invention. When employed, they are typically present from 0.1 to 20% and particularly from 0.5 to 10%, based on the total weight of the composition.
- Preferred co-conditioners include fatty esters, and fatty N-oxides.
- Fatty esters that may be employed include fatty monoesters, such as glycerol monostearate, fatty sugar esters, such as those disclosed in WO 01/46361 (Unilever) .
- the composition of the invention may optionally contain one or more of the ingredients including preservatives (e.g.
- bactericides pH buffering agents, fluorescers, colourants, hydrotropes, antifoaming agents, anti- redeposition agents, soil-release agents, polyelectrolytes, enzymes, optical brightening agents, anti-shrinking agents, anti-wrinkle agents, anti- spotting agents, anti-oxidants, sunscreens, anti- corrosion agents, drape imparting agents, anti-static agents, ironing aids and dyes.
- Composition of the present invention can be prepared using any conventional liquid mixing equipment.
- the process of manufacture involves addition of all the ingredients of the composition and mixing.
- the processing may be carried out at temperature between 10- 80° C, more preferably in the range 30-60° C.
- composition according to the present invention were prepared using following ingredients .
- Cetyl trimethyl ammonium chloride (hereinafter referred to as C16-TAC) , available under trade name CTAC 30 KC having 30 % purity, Stearyl trimethyl ammonium chloride (hereinafter referred to as C18- TAC) , available under trade name STAC 80 KC having 80 % purity, and Behenyl trimethyl ammonium chloride (hereinafter referred to as C22-TAC) , available under trade name BTAC 80 KC, having 80 % purity were procured from KCL, Korea: Ethylene glycol was procured from Manali Petrochemicals, India. Fatty alcohol ethoxylate was procured from Cognis, (Trade name is Dehydol -100) . Fragrance was procured from Givaudan Roure .
- composition of the present invention (Examples A, B, C, D, E and F) were found to be visually clear.
- Examples A, B, C, D, E and F showed a good fabric softening and fragrance retention performance.
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- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Emergency Medicine (AREA)
- Detergent Compositions (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Abstract
A clear or translucent fabric conditioner composition comprising: (a) 0.1-30% by weight a quaternary ammonium fabric conditioner active of the formula RR1R2R3N+X', wherein R is alkyl group having 16 to 22 carbon atoms, R1, R2 and R3 are alkyl groups having 1 to 4 carbon atoms, and X is anion selected from chloride, bromide, acetate, sulfate, nitrate, and phosphate; (b) 0.1-15 % by weight hydrotrope selected from fatty alcohol ethoxylates and alkylene polyols or mixtures thereof ; 0.001-10% by weight fragrance; and (c) 45-99 % by weight water wherein nonaqueous solvents including short chain C1-C6 alcohols, C1-C4 alkylene carbonates and short chain C2-C8 alkyl ethers are at levels not greater than 10% by weight of the composition.
Description
Clear Fabric Conditioner Composition
Technical Field
This invention relates to clear or translucent fabric conditioner composition. The composition of the present invention has reduced amount of non-aqueous solvent.
Background and Prior Art
Fabric conditioners are well known in the art. Fabric conditioners that are clear or translucent have a better visual appeal and are being increasingly preferred by consumers. Consequently, various approaches have been used in the prior art to produce clear or translucent fabric conditioners .
GB2211510 (Colgate-Palmolive Company, 1989) teaches fabric conditioning and antistatic detergent compositions or softergents which include 10-35% by weight a narrow range ethoxylate nonionic detergent, 2- 15% by weight a fabric conditioning and antistatic cationic compound such as Ci2-Ci8 quaternary ammonium halide and 30-70% by weight water. The compositions of this prior art invention are superior in detersive action compared to identical compositions except for replacement of the narrow range ethoxylate with a broad range ethoxylate nonionic detergent . The superior detersive action is attributed to the presence of the
narrow range ethoxylated nonionic detergent that are believed to counteract the negative effect of quaternary ammonium halide on detergency. This invention of is directed at improving detergency of fabric conditioner compositions .
US005399272 (Procter & Gamble Company, 1995) teaches fabric conditioning compositions comprising 20-80% by weight of fabric conditioner active, 2-25% C8-C22 monoalkyl cationic quaternary ammonium compound dispersibility aid and 17-75% non-aqueous solvent, wherein the fatty acyl components of the fabric conditioner active have an average Iodine Value of at least 50. The use of C8-C22 quaternary ammonium compounds has been taught as an auxiliary ingredient to the fabric conditioner active as a dispersibility aid.
EP1149891 (Goldschmidt Chemical Company, 2001) teaches aqueous laundry detergent compositions comprising a blend of quaternary ammonium fabric conditioner actives 1-50% by weight of at least one anionic scavenger and 50-99% by weight of at least on triglyceride based ester quat . The use of C8-C22 quaternary ammonium compounds has been taught as an auxiliary ingredient to the fabric conditioner active as an anionic scavenger.
One of the difficulties in formulating clear or translucent fabric conditioner composition is that incorporation of fragrance, typically containing a large fraction of hydrophobic water-insoluble compounds,
causes turbidity. Attempts to formulate clear or translucent fabric conditioner composition comprising fragrance have necessitated use of expensive fabric conditioner actives that have higher solubility as compared to conventional conditioner actives and/or the use of non-aqueous solvents at a high level in the formulation that may not be desirable from environmental and safety points of view. Thus there is a clear and distinct need to develop clear or translucent fabric conditioner composition that comprises less expensive fabric conditioner actives and yet contains lower amounts of non-aqueous solvents.
Therefore one of the objects of the present invention is to devise clear or translucent fabric conditioner composition comprising fragrance which is based on less expensive fabric conditioner actives .
Another object of the present invention is to devise clear or translucent fabric conditioner composition that has reduced level of non-aqueous solvents, preferably below 10% by weight.
It has been now surprisingly found that it is possible to devise clear or translucent fabric conditioner compositions comprising fragrance which are based on less expensive fabric conditioner actives and reduced amount of non-aqueous solvents.
Summary of the Invention
According to the present invention there is provided a clear or translucent fabric conditioner composition comprising
0.1-30% by weight a quaternary ammonium fabric conditioner active of the formula RR1R2R3N+X", where, R is an alkyl group with 16 to 22 carbon atoms, R1, R2 and R3 are alkyl groups with 1 to 4 carbon atoms, X is a an anion selected from chloride, bromide, acetate, sulfate, nitrate, and phosphate;
0.1-15 % by weight a hydrotrope selected from fatty alcohol ethoxylates and alkylene polyols or mixtures thereof;
0.001-10% by weight fragrance; and
45-99 % by weight water;
wherein nonaqueous solvents including short chain C1-C6 alcohols, Ci-C4 alkylene carbonates and short chain C2-C8 alkyl ethers are at levels not greater than 10% by weight of the composition.
Detailed Description of the Invention
As stated above, the present invention is directed to a clear or translucent fabric conditioner composition comprising quaternary ammonium fabric conditioner
active, hydrotrope, fragrance and water. The composition of the present invention is visually clear. Within the context of this invention, a composition is termed as clear or translucent when the light transmittance at 600 nm is greater than 80%. The composition of the present invention preferably has a viscosity between 20-200 cP at a shear rate of 106 s"1.
Quaternary Ammonium Fabric conditioner actives
The composition of the present invention comprises of quaternary ammonium fabric conditioner active, preferably 0.1-30%, more preferably 3-22% by weight. The quaternary ammonium fabric conditioner active of the present invention is of the general formula RR1R2R3N+X", where R is an alkyl group with 16 to 22 carbon atoms, R1, R2 and R3 are alkyl groups with 1 to 4 carbon atoms, and X is a an anion selected from chloride, bromide, acetate, sulfate, nitrate, and phosphate.
Particularly preferred is a composition comprising at least two quaternary ammonium fabric conditioner actives wherein number of carbon atoms in R group of the actives is different.
Preferred quaternary ammonium fabric conditioner actives are the mono long-chain alkyl quaternary fabric conditioner actives where R1, R2 and R3 each are methyl groups and R is an alkyl group with 16 to 22 carbon atoms.
The anion of the quaternary fabric conditioner actives is selected from chloride, bromide, acetate, sulfate, nitrate, and phosphate. Chloride salt of quaternary ammonium fabric conditioner actives is particularly preferred.
The most preferred quaternary ammonium fabric conditioner actives of the present invention are cetyl trimethyl ammonium chloride, stearyl trimethyl ammonium chloride and behenyl trimethyl ammonium chloride .
It is preferred that when R is alkyl group having 16 carbon atoms, the active is present in an amount in the range of 0.5 to 10% by weight of the composition, when R is alkyl group having 18 carbon atoms, the active is present in an amount in the range of 1 to 20% by weight of the composition, and when R is alkyl group with 22 carbon atoms, the active is present in an amount in the range of 0.1 to 10% by weight of the composition.
Conventional cationic fabric conditioner actives
It is particularly preferred that other conventional cationic fabric conditioner actives are not greater than 1% by weight of the composition. More preferably, the inventive composition is substantially free of other conventional cationic fabric conditioner actives such as triglyceride-based ester quaternary ammonium compounds, ester quaternary ammonium compounds, and saturated or
unsaturated ditallow dimethyl quaternary ammonium compounds .
Hydrotropes
The composition of the present invention preferably comprises 0.1-15 % by weight hydrotrope selected from fatty alcohol ethoxylates and alkylene polyols or mixtures thereof .
Preferred fatty alcohol ethoxylates of the present invention are Ci2-Ci8 alcohol ethoxylate having 1-20 oxyethylene units on an average.
Alkylene polyols of the present invention are preferably C2-C10 polyhydric alcohols, more preferably C2-C6 alkylene glycols. Some examples of the polyhydric alcohols of the present invention include ethylene glycol, glycerol and hexylene glycol .
Fragrance
The term fragrance, for the purpose of this invention, means a mixture of odoriferous components, optionally mixed with a suitable solvent diluent or carrier, which is employed to impart a desired odor.
Fragrance components and mixtures thereof may be obtained from natural products such as essential oils, absolutes, resinoids, resins and concretes, as well as
synthetic products such as hydrocarbons, alcohols, aldehydes, ketones, ethers, carboxylic acids, esters, acetals, ketals, lactones, sulphides, halides, oximes, nitriles and the like, including saturated and unsaturated compounds, aliphatic, aromatic and heterocyclic compounds.
Typical fragrance ingredients which may be employed in the present invention are selected from one or more of; 2-Methoxy naphthalene, Allyl cyclohexylpropionate, citronellal, alpha-Ionone, alpha- Santalol, alpha- Terpineol, Ambrettolide, Amyl benzoate, Amyl cinnamate, Amyl cinnamic aldehyde, Aurantiol, Benzaldehyde, Benzophenone, Benzyl acetate, Benzyl salicylate, Beta- caryophyllene, Beta-Methyl naphthyl ketone, Cadinene, Cavacrol, Cedrol , Cedryl acetate, Cedryl formate, 2 Cinnamyl cinnamate, cis-Jasmone, Coumarin, Cyclamen aldehyde, Cyclohexyl salicylate, d-Limonene, delta- Nonalactone, delta-Undecalactone, Dihydro isojasmonate, Dibydro mycenol, Dimethyl acetal , Diphenyl methane, Diphenyl oxide, Dodecalactone, Ethyl methyl phenyl glycidate, Ethyl undecylenate, Ethylene brassylate, Eugenol , Exaltolide, Galaxolide, gamma-methyl Ionone, gamma-Undecalactone, Geraniol , Geranyl acetate, Geranyl anthranilate, Geranyl phenyl acetate, Hexadecanolide , Hexenyl salicylate, Hexyl cinnamic aldehyde, Hexyl salicylate, Hydroxycitronellal , Indole, Iso E super, Iso-Amyl salicylate, Iso-Bornyl acetate, Iso-Butyl quinoline, Iso-Eugenol, Lactone, Laevo-Carvone, Lilial (p-t-bucinal) , Linalool, Linalyl acetate, Linalyl
benzoate, Methyl cinnamate, Methyl dihydrojasmonate, Methyl-N-methyl anthranilate, Musk indanone, Musk ketone, Musk tibetine, Nerol , Oxahexadecanolide-10, Oxahexadecanolide-11, para-Cymene, para-tert-Butyl cyclohexyl acetate, Patchouli alcohol, Phantolide, Phenyl ethyl alcohol, Phenyl ethyl benzoate, Phenyl heptanol, Phenylhexanol , Phenylethylphenylacetate, Thibetolide, Vanillin, Vertenex, Vetiveryl acetate, Yara-yara and Ylangene.
Other preferred fragrance ingredients are cyclic and acyclic terpenes and terpenoids. These materials are based upon isoprene repeating units. Examples include alpha and beta pinene, myrcene, geranyl alcohol and acetate, camphene, 10 dl-limonene, alpha and beta phellandrene, tricyclene, terpinolene, allocimmane, geraniol, nerol, linanool, dihydrolinanool, citral, ionone, methyl ionone, citronellol, citronella!, alpha terpineol, beta terpineol, alpha fenchol, borneol, isoborneol, camphor, terpinen-1-ol , terpin-4-ol, 15 dihydroterpineol , methyl chavicol, anethole, 1, 4 and 1, 8 cineole, geranyl nitrile, isobornyl acetate, linalyl acetate, caryophyllene, alpha cedrene, guaiol, patchouli alcohol, alpha and beta santalol and mixtures thereof.
Suitable solvents, diluents or carriers for fragrance ingredients as mentioned above are for example ethanol, isopropanol, diethylene glycol monoethyl ether, dipropyl glycol and triethyl citrate.
The composition of present invention preferably comprises 0.001-10% by weight, more preferably 1-5% by weight of fragrance.
Water
The fabric conditioner composition preferably comprises 45-99%, more preferably 75-90% water by weight.
Non-aqueous organic solvents
It is particularly preferred that nonaqueous organic solvents are not greater than 10% by weight of the composition. Nonaqueous organic solvents include short chain Ci-C6 alcohols, Ci-C4 alkylene carbonates and short chain C2-C8 alkyl ethers.
Co-conditioner
Co-conditioners can be optionally used together with the cationic conditioning actives of the present invention. When employed, they are typically present from 0.1 to 20% and particularly from 0.5 to 10%, based on the total weight of the composition. Preferred co-conditioners include fatty esters, and fatty N-oxides. Fatty esters that may be employed include fatty monoesters, such as glycerol monostearate, fatty sugar esters, such as those disclosed in WO 01/46361 (Unilever) . The composition of the invention may optionally contain one or more of the ingredients including preservatives
(e.g. bactericides), pH buffering agents, fluorescers, colourants, hydrotropes, antifoaming agents, anti- redeposition agents, soil-release agents, polyelectrolytes, enzymes, optical brightening agents, anti-shrinking agents, anti-wrinkle agents, anti- spotting agents, anti-oxidants, sunscreens, anti- corrosion agents, drape imparting agents, anti-static agents, ironing aids and dyes.
Examples
Composition of the present invention can be prepared using any conventional liquid mixing equipment. The process of manufacture involves addition of all the ingredients of the composition and mixing. The processing may be carried out at temperature between 10- 80° C, more preferably in the range 30-60° C.
A few examples of the composition according to the present invention were prepared using following ingredients .
Cetyl trimethyl ammonium chloride (hereinafter referred to as C16-TAC) , available under trade name CTAC 30 KC having 30 % purity, Stearyl trimethyl ammonium chloride (hereinafter referred to as C18- TAC) , available under trade name STAC 80 KC having 80 % purity, and Behenyl trimethyl ammonium chloride (hereinafter referred to as C22-TAC) , available under trade name BTAC 80 KC, having 80 % purity were procured from KCL, Korea:
Ethylene glycol was procured from Manali Petrochemicals, India. Fatty alcohol ethoxylate was procured from Cognis, (Trade name is Dehydol -100) . Fragrance was procured from Givaudan Roure .
Examples of the composition that are within the scope of the present invention are given in Table 1.
TABLE 1
The composition of the present invention (Examples A, B, C, D, E and F) were found to be visually clear. Examples A, B, C, D, E and F showed a good fabric softening and fragrance retention performance.
Claims
l.A clear or translucent fabric conditioner composition comprising:
(a) 0.1-30% by weight a quaternary ammonium fabric conditioner active of the formula RR1R2R3N+X", wherein R is alkyl group having 16 to 22 carbon atoms, R1, R2 and R3 are alkyl groups having 1 to 4 carbon atoms, and X is anion selected from chloride, bromide, acetate, sulfate, nitrate, and phosphate;
(b) 0.1-15 % by weight hydrotrope selected from fatty alcohol ethoxylates and alkylene polyols or mixtures thereof ; 0.001-10% by weight fragrance; and
(c) 45-99 % by weight water
wherein nonaqueous solvents including short chain Cx-C6 alcohols, Ci-C4 alkylene carbonates and short chain C2-C8 alkyl ethers are at levels not greater than 10% by weight of the composition.
2. A clear or translucent fabric conditioner composition as claimed in claim 1 comprising at least two of said active, wherein numbers of carbon atoms in R group of the actives are different.
3. A clear or translucent fabric conditioner composition as claimed in claim 1 or claim 2, wherein conventional cationic fabric conditioner actives including triglyceride-based ester quaternary ammonium compounds, ester quaternary ammonium compounds, and saturated or unsaturated ditallow dimethyl quaternary ammonium compounds are not greater than 1% by weight of said composition.
4. A clear or translucent fabric conditioner composition as claimed in any one of the preceding claims, wherein said active is present at 3-22% by weight of the composition.
5.A clear or translucent fabric conditioner composition as claimed in any one of the preceding claims, wherein R1, R2, and R3 are methyl groups.
6. A clear or translucent fabric conditioner composition as claimed in any one of the preceding claims, wherein the anion is chloride.
7. A clear or translucent fabric conditioner composition as claimed in any one of the preceding claims, wherein said fatty alcohol ethoxylate is Ci2-Ci8 alcohol ethoxylate having 1-20 oxyethylene units .
8. A clear or translucent fabric conditioner composition as claimed in any one of the preceding claims, wherein the said alkylene polyol is C2-Ci0 polyhydric alcohol .
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
IN1636MU2005 | 2005-12-29 | ||
PCT/EP2006/012066 WO2007073877A1 (en) | 2005-12-29 | 2006-12-08 | Clear fabric conditioner composition |
Publications (1)
Publication Number | Publication Date |
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EP1969107A1 true EP1969107A1 (en) | 2008-09-17 |
Family
ID=37734055
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP06829617A Ceased EP1969107A1 (en) | 2005-12-29 | 2006-12-08 | Clear fabric conditioner composition |
Country Status (6)
Country | Link |
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EP (1) | EP1969107A1 (en) |
CN (1) | CN101370918A (en) |
AR (1) | AR058879A1 (en) |
BR (1) | BRPI0620777A2 (en) |
WO (1) | WO2007073877A1 (en) |
ZA (1) | ZA200805603B (en) |
Families Citing this family (7)
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US8648027B2 (en) | 2012-07-06 | 2014-02-11 | The Clorox Company | Low-VOC cleaning substrates and compositions comprising a cationic biocide |
US9096821B1 (en) | 2014-07-31 | 2015-08-04 | The Clorox Company | Preloaded dual purpose cleaning and sanitizing wipe |
US10975341B2 (en) | 2017-09-18 | 2021-04-13 | The Clorox Company | Cleaning wipes having particular MABDF characteristics |
US10973385B2 (en) | 2017-09-18 | 2021-04-13 | The Clorox Company | Cleaning wipes having particular pore volume distribution characteristics |
US10982177B2 (en) | 2017-09-18 | 2021-04-20 | The Clorox Company | Cleaning wipes with particular lotion retention and efficacy characteristics |
US10973386B2 (en) | 2017-09-18 | 2021-04-13 | The Clorox Company | Cleaning wipes system having particular performance characteristics |
US11273625B2 (en) | 2018-12-21 | 2022-03-15 | The Clorox Company | Process for manufacturing multi-layer substrates comprising sandwich layers and polyethylene |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
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AU616438B2 (en) * | 1987-10-27 | 1991-10-31 | Colgate-Palmolive Company, The | Antistatic and fabric softening liquid detergent composition |
ZA991635B (en) * | 1998-03-02 | 1999-09-02 | Procter & Gamble | Concentrated, stable, translucent or clear, fabric softening compositions. |
AU2005253926B2 (en) * | 2004-06-08 | 2010-07-22 | Dow Global Technologies Inc. | Ethanol-free aqueous perfume composition |
-
2006
- 2006-12-08 CN CNA2006800495154A patent/CN101370918A/en active Pending
- 2006-12-08 EP EP06829617A patent/EP1969107A1/en not_active Ceased
- 2006-12-08 ZA ZA200805603A patent/ZA200805603B/en unknown
- 2006-12-08 BR BRPI0620777-4A patent/BRPI0620777A2/en not_active IP Right Cessation
- 2006-12-08 WO PCT/EP2006/012066 patent/WO2007073877A1/en active Application Filing
- 2006-12-28 AR ARP060105845A patent/AR058879A1/en unknown
Non-Patent Citations (1)
Title |
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See references of WO2007073877A1 * |
Also Published As
Publication number | Publication date |
---|---|
ZA200805603B (en) | 2009-10-28 |
AR058879A1 (en) | 2008-02-27 |
WO2007073877A1 (en) | 2007-07-05 |
CN101370918A (en) | 2009-02-18 |
BRPI0620777A2 (en) | 2011-11-22 |
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