WO1999042547A1 - Stable rinse cycle fabric softener composition with glycerol monostearate co-softener - Google Patents

Stable rinse cycle fabric softener composition with glycerol monostearate co-softener Download PDF

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Publication number
WO1999042547A1
WO1999042547A1 PCT/US1999/003378 US9903378W WO9942547A1 WO 1999042547 A1 WO1999042547 A1 WO 1999042547A1 US 9903378 W US9903378 W US 9903378W WO 9942547 A1 WO9942547 A1 WO 9942547A1
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WO
WIPO (PCT)
Prior art keywords
fabric softener
composition
softener composition
quaternary ammonium
emulsifier
Prior art date
Application number
PCT/US1999/003378
Other languages
French (fr)
Inventor
Jose Javier Tovar Pescador
Salvador Jantes Hernandez
Alain Jacques
Original Assignee
Colgate-Palmolive Company
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
Priority claimed from US09/237,528 external-priority patent/US6057285A/en
Priority to NZ500399A priority Critical patent/NZ500399A/en
Priority to CA002287514A priority patent/CA2287514A1/en
Priority to AU27692/99A priority patent/AU2769299A/en
Priority to JP54267899A priority patent/JP2001525020A/en
Priority to SK1549-99A priority patent/SK154999A3/en
Application filed by Colgate-Palmolive Company filed Critical Colgate-Palmolive Company
Priority to BR9904829-9A priority patent/BR9904829A/en
Priority to EP99908200A priority patent/EP0975726A1/en
Priority to HU0003822A priority patent/HUP0003822A3/en
Priority to IL13233299A priority patent/IL132332A/en
Publication of WO1999042547A1 publication Critical patent/WO1999042547A1/en
Priority to BG103896A priority patent/BG103896A/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
    • C11D1/66Non-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
    • C11D1/38Cationic 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
    • C11D1/66Non-ionic compounds
    • C11D1/72Ethers of polyoxyalkylene glycols

Definitions

  • This invention relates to liquid fabric softening compositions intended for use in the rinse cycle of an automatic fabric washing machine and for hand use. More particularly, this invention is concerned with aqueous fabric softening compositions which provide improved softness to fabrics concomitant with improved product stability as manifested by properties such as uniform viscosity over a wide range of temperature and avoidance of phase separation.
  • compositions containing quaternary ammonium salts are commonly used to provide fabric softening benefits when used in a laundry rinse operation. Numerous patents have been issued for these types of compounds and compositions.
  • R groups represent an aliphatic ester residue of from 12 to 30 carbon atoms, and the remaining R groups represent lower aliphatic, aryl or hydroxyalkyl groups
  • X" is an anion and "a” represents the ionic valence of the anion
  • R! is a C12 to C30 alkyl or alkenyl group
  • R ⁇ represents Rl,RlCONH(CH2) m or CH2CH2OH
  • R ⁇ represents hydrogen, methyl, or (CH2CH2 ⁇ )pH
  • m is a number of 1 to 5
  • p is a number of 1 to 5, at a weight ratio of ester quat to amidoamine of from 10:1 to 1:10.
  • U.S. Patent 4,844,823 to Jacques et al discloses fabric softener compositions wherein a preferred class of softeners are the diesterified long chain fatty acid quaternary ammonium compounds.
  • Glycerol monostearate is a known emulsifier for the aforementioned esterified quaternary ammonium softeners, commonly referred to as "ester quat” softeners.
  • ester quat is a mono or di-ester variation of ditallow dimethyl ammonium chloride (DTDMAC) in combination with glycerol monostearate and a linear alkoxylated alcohol selected from the condensation products of C 8 -C 18 linear fatty alcohols with from 1 to about 10 moles of ethylene oxide.
  • DTDMAC ditallow dimethyl ammonium chloride
  • U.S. Patent 5,545,350 to Baker et al describes fabric softener compositions comprised of a diester quaternary ammonium compound optionally further containing a nonionic softener such as a sorbitan ester as an additional softening agent.
  • a nonionic softener such as a sorbitan ester
  • the patentees indicate that "glycerol monostearate having a low HLB has a detrimental effect on stability of the compositions.”
  • the patentees state that "the compositions of the present invention are essentially free of glycerol monostearate (GMS)." The reason provided is that the low HLB of GMS causes phase separation and/or stability problems in the compositions described in the patent.
  • a stable, pourable and water dispersible fabric softener composition comprising:
  • each R 4 independently represents an aliphatic hydrocarbon group having from 8 to 22 carbon atoms
  • R 5 represents (CH 2 ) S — R 7 where R 7 represents an alkoxy carbonyl group containing from 8 to 22 carbon atoms, benzyl, phenyl,
  • an effective amount of an emulsifier comprising a fatty alcohol ethoxylate nonionic surfactant having a hydrophilic-lipophilic balance (HLB) value greater than about 7.5 as measured by the Davies Group number method; and
  • the present invention also provides a method of imparting softness to fabrics by contacting the fabrics with a softening effective amount of the fabric softener composition of the invention; generally and preferably, in the rinse cycle of an automatic laundry washing machine.
  • the present invention is predicated on the discovery that glycerol monostearate (GMS) can be used effectively as a co-softener in conjunction with a diester quaternary ammonium compound as herein described without adversely affecting viscosity and overall product stability with the proviso that an emulsifier is selected in accordance with the invention having an HLB value of greater than 7.5.
  • GMS glycerol monostearate
  • the HLB value is calculated for purposes of the present invention using the Davies group number values as described in Proceedings 2 nd Intern. Congress on Surface Activity, Butterworths, London (1957). According to this method of calculation, an HLB value of 7 signifies that a surfactant has the same affinity for the aqueous phase as for the oily phase. Negative values are assigned to the lipophilic groups in the molecule and positive values to the hydrophilic groups. The HLB of a given surfactant is calculated by adding to the number 7 the sum of the positive values representing the hydrophilic groups and by subtracting the negative values representing the hydrophobic groups.
  • the fatty alcohol ethoxylate nonionic surfactant which is used as the emulsifier in the composition of the invention has the following assigned Davies group number values for the groups present in the surfactant molecule.
  • the HLB of a nonionic surfactant emulsifier useful herein, C 13 - C 15 EO 20:1 is calculated as shown below.
  • This nonionic surfactant is a fatty alcohol having an average of 13 to 15 carbon atoms ethoxylated with 20 moles of ethylene oxide per mole of alcohol.
  • the length of the alkyl chain is averaged at C 14 .
  • the resulting molecule is then comprised of the following groups: 1 CH 3 -; 13 -CH 2 -; 1 -O-; and 20 - (CH 2 - CH 2 - O) -
  • the principal softening compound according to the invention is the fatty ester quaternary ammonium compound having the following formula:
  • Each R4 independently represents an aliphatic hydrocarbon group having from 8 to 22 carbon atoms, and preferably 14 to 18 carbon atoms.
  • Rg represents (CH 2 ) t Rg as defined above.
  • the fatty ester quaternary compounds are diester compounds, i.e. R7 represents benzyl, phenyl, phenyl substituted by C1-C4 alkyl, hydroxyl (OH) or hydrogen
  • R7 represent OH or H, especially preferably OH, e.g. R5 is hydroxyethyl.
  • q, r and s, each, independently, represents a number of from 1 to 3.
  • X represents a counter ion of valence a such as Cl “ , Br “ , CH 3 OSO 3 " , CH 3 CH 2 OSOJ, and the like.
  • the diester quat of formula (II) may be a compound of the formula: CH 2 CH 2 OH O
  • each R4 may be, for example, derived from hard or soft tallow, coco, stearyl, oleyl, and the like.
  • Such compounds are commercially available as, for example, Tetranyl AT-75, from Kao Corp. Japan, which is di-tallow ester triethanol amine quaternary ammonium methyl sulfate.
  • Tetranyl AT-75 is based on a mixture of about 25% hard tallow and about 75% soft tallow. Accordingly, this product contains about 34% of unsaturated alkyl chains.
  • a second example would be Hipochem X-89107, from High Point Chemical Corp.; which is an analogue of the Tetranyl AT-75 with about 100% saturation in the tallow moieties.
  • the quatemized ammonium ester compound of formula (III) may contain from about 5% to about 75% of unsaturated (long-chain) alkyl groups.
  • Glycerol monostearate is the co-softener used in combination with the fatty ester quaternary ammonium compound softener described above.
  • the range of fatty ester quat in the composition will generally vary from about 1% to about 20%, by weight, of the composition; preferably a range of from about 1% to about 12%; and most preferably a range of from about 2% to about 10%, by weight.
  • the amount of GMS in the composition will vary from about 0.1% to about 8%, by weight; preferably from about 0.5% to about 8%, by weight, and most preferably from about 0.5% to about 5%, by weight.
  • the emulsifier used in the present fabric softening composition is required to stabilize the composition and prevent phase separation and/or an unstable viscosity over a period of at least several months or over a range of temperatures wherein such composition would otherwise be destabilized by the presence of the GMS in the composition in the absence of such emulsifier.
  • the fatty alcohol ethoxylates useful in the invention correspond to ethylene oxide condensation products of higher fatty alcohols, with the higher fatty alcohol being of from about 9 to 15 carbon atoms and the number of ethylene oxide groups per mole being from about 10 to 30.
  • the alkyl chain length ranges from about 13 to 15 carbon atoms and the number of ethylene groups ranges from about 15 to 20 per mole.
  • Synperonic A20 is Especially preferred for use herein.
  • nonionic surfactant being an ethoxylated C 13 -C 15 fatty alcohol with 20 moles of ethylene oxide per mole of alcohol and having an HLB of 8.25.
  • the HLB of the nonionic fatty alcohol ethoxylates are from about 7.5 to about 10, with an HLB range of from about 8 to about 9 being preferred. They are used in the composition in sufficient amount to provide emulsification, typically from about 1 to 5%, by weight of the composition.
  • compositions of this invention are provided as aqueous dispersions in which the fabric softener compounds are present in finely divided form stably dispersed in the aqueous phase.
  • particle sizes of the dispersed particles of less than about 25 microns ( ⁇ m), preferably less than 20 ⁇ m, especially preferably no more than 10 ⁇ m, on average are acceptable for both softening and stability insofar as the particle sizes can be maintained during actual use, typically in the rinse cycle of an automatic laundry washing machine.
  • the aqueous phase of the dispersion is primarily water, usually deionized or distilled water. Small amounts (e.g. up to about 5% by weight) of co-solvent may be present for adjustment of viscosity.
  • co-solvent lower mono- and poly-hydroxy alcohols will be used, generally in amounts up to about 5% by weight of the composition.
  • the preferred alcohols and aqueous are those having from 2 to 4 carbon atoms, such as, for example, ethanol, propanol, isopropanol, and propylene glycol or ethylene glycol. Isopropyl alcohol (2 -propanol) is especially preferred.
  • co-solvents are not required and are generally avoided.
  • compositions of this invention include an electrolyte to reduce dispersion viscosity.
  • any of the alkaline metals or alkaline earth metal salts of the mineral acids can be used as electrolyte.
  • solubility and low toxicity NaCl, CaCl2, MgCl2 and MgSO4 and similar salts of alkaline and alkaline earth metals are preferred, and CaCl2 is especially preferred.
  • the amount of the electrolyte will be selected to assure that the composition does not form a gel.
  • amounts of electrolyte salt of from about 0.05 to 2.0 wt%, preferably 0.1 to 1.5 wt%, especially preferably 0.25 to 1.4 wt%, will effectively prevent gelation from occurring.
  • the fabric softener compositions of the invention are formulated to be free of an inorganic mineral acid as well as an organic acid because the presence of such acid ingredients may adversely affect the desired rheology and/or stability of the resulting composition.
  • Optional components commonly used in fabric softening compositions may be added in minor amounts to enhance either the appearance or performance properties of the liquid fabric softener compositions of this invention.
  • Typical components of this type include, but are not limited to colorants, e.g., dyes or pigments, rheology modifiers, color protection agents, stain-guard agents, preservatives, germicides, and perfumes.
  • final product viscosity (for a freshly prepared sample) should not exceed about 400 centipoise, preferably not more than 300 centipoise, but should not be too low, for example not less than about 50 centipoise.
  • the preferred viscosity for the invention concentrated product is in the range of 120 to 300 centipoise. As used herein, unless otherwise specified, viscosity is measured at 25°C (22-26°C) using a Brookfield RVTD Digital Niscometer with Spindle #2 at 50 rpm.
  • Example 1 A method of preparation of a compositions of the invention (Composition D) is described below.
  • Water was heated to 60°C and then the dye, the Dequest sequestrant and the nonionic emulsifier were dissolved in the heated water to form a first part.
  • the diesterquat softener and the glycerol monostearate were melted and blended with a mixer at 60°C.
  • the resulting homogeneous blend was then dispersed under agitation into the above described first part. Mixing was maintained for about 10 minutes until a homogeneous emulsion was formed.
  • the resulting emulsion was allowed to cool at 25°C while maintaining agitation.
  • compositions A, B and C Three softening compositions were prepared as described in Example 1 based on diester quat and GMS and are designated compositions A, B and C.
  • composition A Composition B
  • Composition C Composition B
  • Composition A is in accordance with the invention and contained Synperonic A20 as the emulsifier;
  • Composition B is a comparative composition which contained as the emulsifier a fatty alcohol ethoxylate C 16 -C 18 fatty alcohol with 19 moles of ethylene oxide and having an HLB value of 6.5.
  • Composition C is a comparative composition which contained as the emulsifier a fatty alcohol ethoxylate C 12 -C 13 fatty alcohol with 3 moles of ethylene oxide having an HLB value of 1.81.
  • the three compositions were prepared as described above and the viscosity was measured directly after making; after 1 day; and after 6 weeks at temperatures of 4°C, room temperature; 35°C; and 43°C. The results are shown in Table 2.
  • composition A Composition B
  • Composition C Composition B

Abstract

Rinse cycle fabric softeners are described which are stable and pourable and which contain a quaternary diester fabric softener such as N-methyl, N,N,N-triethanolamine ditallowester quaternary ammonium salt in combination with glycerol monostearate and a fatty alcohol ethoxylate nonionic surfactant as the emulsifier having an HLB value above 7.5.

Description

STABLE RINSE CYCLE FABRIC SOFTENER COMPOSITION WITH GLYCEROL MONOSTEARATE CO-SOFTENER
Field of the Invention
This invention relates to liquid fabric softening compositions intended for use in the rinse cycle of an automatic fabric washing machine and for hand use. More particularly, this invention is concerned with aqueous fabric softening compositions which provide improved softness to fabrics concomitant with improved product stability as manifested by properties such as uniform viscosity over a wide range of temperature and avoidance of phase separation.
Compositions containing quaternary ammonium salts are commonly used to provide fabric softening benefits when used in a laundry rinse operation. Numerous patents have been issued for these types of compounds and compositions.
More recently, however, in view of concerns for the environmental safety (e.g. biodegradability) of the quaternary ammonium compound softeners, there have been many proposals for partial or total replacement of the conventional "quat" fabric softener which are exemplified by dimethyl distearyl (or ditallow) ammonium chloride.
For instance, in U.S. Patent 5,133,885 to L. Contor, et al. (corresponding to EP 0423894, both assigned to Colgate-Palmolive Company, the assignee of the present invention) fabric softening compositions are described which are aqueous dispersions of a fatty acid ester quat of formula:
R R
X
N+
R R
where one or two R groups represent an aliphatic ester residue of from 12 to 30 carbon atoms, and the remaining R groups represent lower aliphatic, aryl or hydroxyalkyl groups, X" is an anion and "a" represents the ionic valence of the anion, and a fatty acid amidoamine softener of formula:
1 R1CONH(CH2)mN-R3
R2
where R! is a C12 to C30 alkyl or alkenyl group, R^ represents Rl,RlCONH(CH2)m or CH2CH2OH; R^ represents hydrogen, methyl, or (CH2CH2θ)pH, m is a number of 1 to 5 and p is a number of 1 to 5, at a weight ratio of ester quat to amidoamine of from 10:1 to 1:10. U.S. Patent 4,844,823 to Jacques et al discloses fabric softener compositions wherein a preferred class of softeners are the diesterified long chain fatty acid quaternary ammonium compounds.
Glycerol monostearate (GMS) is a known emulsifier for the aforementioned esterified quaternary ammonium softeners, commonly referred to as "ester quat" softeners. U.S. Patent 5,066,414 to Chang describes fabric softening compositions containing an ester quat which is a mono or di-ester variation of ditallow dimethyl ammonium chloride (DTDMAC) in combination with glycerol monostearate and a linear alkoxylated alcohol selected from the condensation products of C8-C18 linear fatty alcohols with from 1 to about 10 moles of ethylene oxide.
U.S. Patent 5,545,350 to Baker et al describes fabric softener compositions comprised of a diester quaternary ammonium compound optionally further containing a nonionic softener such as a sorbitan ester as an additional softening agent. At column 13, lines 22-24, the patentees indicate that "glycerol monostearate having a low HLB has a detrimental effect on stability of the compositions." Further, at column 14, lines 65-67, the patentees state that "the compositions of the present invention are essentially free of glycerol monostearate (GMS)." The reason provided is that the low HLB of GMS causes phase separation and/or stability problems in the compositions described in the patent.
Notwithstanding disclosures in the prior art directed to the combination of diester quaternary ammonium compound softeners with a co-softener there remains a need to deliver improved softness to a diester quat softening composition without adversely affecting product stability and viscosity. Summary of the Invention
In accordance with the present invention, there is provided a stable, pourable and water dispersible fabric softener composition comprising:
(a) from about 1% to about 25% by weight of a combination of fabric softening components (A) and (B) wherein (A) is a biodegradable fatty ester quaternary ammonium compound of formula (I):
O +
R. (CH2)q - O - C - R4
N X"
Re (CH2)r - O - C - R4
(I)
O
wherein each R4 independently represents an aliphatic hydrocarbon group having from 8 to 22 carbon atoms,
R5 represents (CH2)S— R7 where R7 represents an alkoxy carbonyl group containing from 8 to 22 carbon atoms, benzyl, phenyl,
(CrC4) - alkyl substituted phenyl, OH or H; R6 represents (CH2)t R8 where R8 represents benzyl, phenyl, (CrC4) alkyl substituted phenyl, OH or H; q, r, s and t, each independently, represent a number of from 1 to 3; and x is an anion of valence a; and (B) is glycerol monostearate;
(b) an effective amount of an emulsifier comprising a fatty alcohol ethoxylate nonionic surfactant having a hydrophilic-lipophilic balance (HLB) value greater than about 7.5 as measured by the Davies Group number method; and
(c) an aqueous solvent, said fabric softener composition being free of an inorganic mineral acid and an organic acid. The present invention also provides a method of imparting softness to fabrics by contacting the fabrics with a softening effective amount of the fabric softener composition of the invention; generally and preferably, in the rinse cycle of an automatic laundry washing machine. The present invention is predicated on the discovery that glycerol monostearate (GMS) can be used effectively as a co-softener in conjunction with a diester quaternary ammonium compound as herein described without adversely affecting viscosity and overall product stability with the proviso that an emulsifier is selected in accordance with the invention having an HLB value of greater than 7.5. The HLB value is calculated for purposes of the present invention using the Davies group number values as described in Proceedings 2nd Intern. Congress on Surface Activity, Butterworths, London (1957). According to this method of calculation, an HLB value of 7 signifies that a surfactant has the same affinity for the aqueous phase as for the oily phase. Negative values are assigned to the lipophilic groups in the molecule and positive values to the hydrophilic groups. The HLB of a given surfactant is calculated by adding to the number 7 the sum of the positive values representing the hydrophilic groups and by subtracting the negative values representing the hydrophobic groups.
For example, the fatty alcohol ethoxylate nonionic surfactant which is used as the emulsifier in the composition of the invention has the following assigned Davies group number values for the groups present in the surfactant molecule. Group Value
- CH2 - -0.475
- CH3 - -0.475
- (CH2 - CH2 - O) - +0.33
Figure imgf000006_0001
- O - +1.3
By way of illustration, the HLB of a nonionic surfactant emulsifier useful herein, C13 - C15 EO 20:1, is calculated as shown below. This nonionic surfactant is a fatty alcohol having an average of 13 to 15 carbon atoms ethoxylated with 20 moles of ethylene oxide per mole of alcohol.
For purposes of simplicity the length of the alkyl chain is averaged at C14. The resulting molecule is then comprised of the following groups: 1 CH3-; 13 -CH2-; 1 -O-; and 20 - (CH2 - CH2 - O) - Based on the above, the HLB is calculated as follows: HLB •= 7 + [1 x (-.475)] + [13 x (-.475)] + [1 x (1.3)] + [20 x (0.33)] HLB - 8.25 Detailed Description of the Invention
The principal softening compound according to the invention is the fatty ester quaternary ammonium compound having the following formula:
o +
R . (CH2)q - O - C - R4
N X"
R6 (CH2)r - O - C - R4
(I)
O
Each R4 independently represents an aliphatic hydrocarbon group having from 8 to 22 carbon atoms, and preferably 14 to 18 carbon atoms. R5 represents the group (CH2)S-R7 which, depending on R7, may represent a long chain alkyl ester group (R7 = Cg-C22 alkoxy carbonyl), in which case the compounds of formula (I) are triester quaternary ammonium compounds. Rg represents (CH2)tRg as defined above.
Preferably, however, the fatty ester quaternary compounds are diester compounds, i.e. R7 represents benzyl, phenyl, phenyl substituted by C1-C4 alkyl, hydroxyl (OH) or hydrogen
(H). Most preferably R7 represent OH or H, especially preferably OH, e.g. R5 is hydroxyethyl. q, r and s, each, independently, represents a number of from 1 to 3.
X represents a counter ion of valence a such as Cl", Br", CH3OSO3 ", CH3CH2OSOJ, and the like. For example, the diester quat of formula (II) may be a compound of the formula: CH2CH2OH O
R4-C-O (CH2)2- ϊf (CH2)2 O-C-R4 CH3SO4 "
(II)
CH,
where each R4 may be, for example, derived from hard or soft tallow, coco, stearyl, oleyl, and the like. Such compounds are commercially available as, for example, Tetranyl AT-75, from Kao Corp. Japan, which is di-tallow ester triethanol amine quaternary ammonium methyl sulfate. Tetranyl AT-75 is based on a mixture of about 25% hard tallow and about 75% soft tallow. Accordingly, this product contains about 34% of unsaturated alkyl chains. A second example would be Hipochem X-89107, from High Point Chemical Corp.; which is an analogue of the Tetranyl AT-75 with about 100% saturation in the tallow moieties. However, in general the quatemized ammonium ester compound of formula (III) may contain from about 5% to about 75% of unsaturated (long-chain) alkyl groups.
Glycerol monostearate (GMS) is the co-softener used in combination with the fatty ester quaternary ammonium compound softener described above. The range of fatty ester quat in the composition will generally vary from about 1% to about 20%, by weight, of the composition; preferably a range of from about 1% to about 12%; and most preferably a range of from about 2% to about 10%, by weight. The amount of GMS in the composition will vary from about 0.1% to about 8%, by weight; preferably from about 0.5% to about 8%, by weight, and most preferably from about 0.5% to about 5%, by weight.
The emulsifier used in the present fabric softening composition is required to stabilize the composition and prevent phase separation and/or an unstable viscosity over a period of at least several months or over a range of temperatures wherein such composition would otherwise be destabilized by the presence of the GMS in the composition in the absence of such emulsifier. The fatty alcohol ethoxylates useful in the invention correspond to ethylene oxide condensation products of higher fatty alcohols, with the higher fatty alcohol being of from about 9 to 15 carbon atoms and the number of ethylene oxide groups per mole being from about 10 to 30. In the preferred fatty alcohol ethoxylates for use herein, the alkyl chain length ranges from about 13 to 15 carbon atoms and the number of ethylene groups ranges from about 15 to 20 per mole. Especially preferred for use herein is Synperonic A20
6 manufactured by ICI Chemicals, such nonionic surfactant being an ethoxylated C13-C15 fatty alcohol with 20 moles of ethylene oxide per mole of alcohol and having an HLB of 8.25.
In general, the HLB of the nonionic fatty alcohol ethoxylates are from about 7.5 to about 10, with an HLB range of from about 8 to about 9 being preferred. They are used in the composition in sufficient amount to provide emulsification, typically from about 1 to 5%, by weight of the composition.
The compositions of this invention are provided as aqueous dispersions in which the fabric softener compounds are present in finely divided form stably dispersed in the aqueous phase. Generally, particle sizes of the dispersed particles of less than about 25 microns (μm), preferably less than 20 μm, especially preferably no more than 10 μm, on average are acceptable for both softening and stability insofar as the particle sizes can be maintained during actual use, typically in the rinse cycle of an automatic laundry washing machine.
The aqueous phase of the dispersion is primarily water, usually deionized or distilled water. Small amounts (e.g. up to about 5% by weight) of co-solvent may be present for adjustment of viscosity. Typically, as the co-solvent lower mono- and poly-hydroxy alcohols will be used, generally in amounts up to about 5% by weight of the composition. The preferred alcohols and aqueous are those having from 2 to 4 carbon atoms, such as, for example, ethanol, propanol, isopropanol, and propylene glycol or ethylene glycol. Isopropyl alcohol (2 -propanol) is especially preferred. However, co-solvents are not required and are generally avoided.
The compositions of this invention include an electrolyte to reduce dispersion viscosity. Generally, any of the alkaline metals or alkaline earth metal salts of the mineral acids can be used as electrolyte. In view of availability, solubility and low toxicity, NaCl, CaCl2, MgCl2 and MgSO4 and similar salts of alkaline and alkaline earth metals are preferred, and CaCl2 is especially preferred. The amount of the electrolyte will be selected to assure that the composition does not form a gel. Generally, amounts of electrolyte salt of from about 0.05 to 2.0 wt%, preferably 0.1 to 1.5 wt%, especially preferably 0.25 to 1.4 wt%, will effectively prevent gelation from occurring.
The fabric softener compositions of the invention are formulated to be free of an inorganic mineral acid as well as an organic acid because the presence of such acid ingredients may adversely affect the desired rheology and/or stability of the resulting composition. Optional components commonly used in fabric softening compositions may be added in minor amounts to enhance either the appearance or performance properties of the liquid fabric softener compositions of this invention. Typical components of this type include, but are not limited to colorants, e.g., dyes or pigments, rheology modifiers, color protection agents, stain-guard agents, preservatives, germicides, and perfumes.
The final product, whether in concentrated or diluted form must be easily pourable by the end user. Generally, therefore, final product viscosity (for a freshly prepared sample) should not exceed about 400 centipoise, preferably not more than 300 centipoise, but should not be too low, for example not less than about 50 centipoise. The preferred viscosity for the invention concentrated product is in the range of 120 to 300 centipoise. As used herein, unless otherwise specified, viscosity is measured at 25°C (22-26°C) using a Brookfield RVTD Digital Niscometer with Spindle #2 at 50 rpm.
Example 1 A method of preparation of a compositions of the invention (Composition D) is described below.
Composition D
Component Weiεht Percent
Ditallow ester triethanol amine quaternary ammonium methyl sulfate 7.33
Glycerol monostearate 1.38
C,3-C15 alcohol EO 20:1 0.6
Dequest 2000 (1) 0.1
Dye 0.002 Calcium chloride 0.05 to 0.5
(as needed for viscosity)
Perfume 0.2-0.8
Water
Figure imgf000010_0001
Balance
(l) A phosphonate sequestering agent marketed by Monsanto Chemical Company
Water was heated to 60°C and then the dye, the Dequest sequestrant and the nonionic emulsifier were dissolved in the heated water to form a first part. In a second vessel, the diesterquat softener and the glycerol monostearate were melted and blended with a mixer at 60°C. The resulting homogeneous blend was then dispersed under agitation into the above described first part. Mixing was maintained for about 10 minutes until a homogeneous emulsion was formed. The resulting emulsion was allowed to cool at 25°C while maintaining agitation.
To the cooled emulsion there was added perfume under agitation. The viscosity of the softener was then adjusted to between 100 to 200 cps by the addition of calcium chloride.
Example 2
To demonstrate the significance with regard to product stability of using an emulsifier in accordance with the invention versus using emulsifiers described in the prior art for use with quaternary ammonium softeners, the following aging tests were conducted.
Three softening compositions were prepared as described in Example 1 based on diester quat and GMS and are designated compositions A, B and C.
Table 1
Composition A Composition B Composition C
Diesterquat 7.33 7.33 7.33
GMS 1.38 1.38 1.38
Perfume 0.2-0.8 0.2-0.8 0.2-0.8
Synperonic A20 0.60
C16-18 19EO 0.60
C12-15 3EO 0.60
Colorant 0.0018 0.0018 0.0018
Preservative 0.2 0.2 0.2
Figure imgf000011_0001
Water up to 100 up to 100 up to 100
Composition A is in accordance with the invention and contained Synperonic A20 as the emulsifier; Composition B is a comparative composition which contained as the emulsifier a fatty alcohol ethoxylate C16-C18 fatty alcohol with 19 moles of ethylene oxide and having an HLB value of 6.5. Composition C is a comparative composition which contained as the emulsifier a fatty alcohol ethoxylate C12-C13 fatty alcohol with 3 moles of ethylene oxide having an HLB value of 1.81. The three compositions were prepared as described above and the viscosity was measured directly after making; after 1 day; and after 6 weeks at temperatures of 4°C, room temperature; 35°C; and 43°C. The results are shown in Table 2.
Table 2
Aging viscosity data for softening compositions as a function of emulsifier HLB
Composition A Composition B Composition C
HLB of emulsifier 8.25 6.5 1.81
After Making 84 cps 107 cps > 800
I Day 116 164 > 800
After 6 Weeks
4°C 176 240 > 800
RT 133 178 > 800
35°C 165 248 > 800
Figure imgf000012_0001
43° 250 436 > 800
As demonstrated in Table 2, only Composition A in accordance with the invention remained stable, below 300 cps, after 6 weeks of aging at 43°C. Compositions B and C were unacceptable because of instability.
Example 3
To demonstrate the significance of the HLB value of the emulsifier with regard to the stability of a diester quat and GMS composition such as shown in Table 1 of Example 2, six compositions are prepared varying only in the particular emulsifier selected. Aging is carried out for 6 weeks at a temperature of 35°C.
The emulsifiers used in each of the six compositions tested are described below in Table 3, which provides the HLB value and the resulting stability of the composition at the conclusion of the aging test.
10 Table 3
Aging stability for softening compositions as a function of the emulsifier HLB (Davies'
Emulsifier HLB Aging Results
C -C1s 20EO 8.25 satisfactory stability
C„-CM25EO 9.9 satisfactory
C-C,„ 30EO 9.7 satisfactory
Clfi-C1R 15EO 4.7 unstable viscosity
C10EO15:1 8.5 satisfactory
Figure imgf000013_0001
C,nEO5:l 4.2 unstable viscosity
11

Claims

ClaimsWhat is claimed is:
1. A stable, pourable and water dispersible liquid fabric softener composition comprising:
(a) from about 1% to about 25% by weight of a combination of fabric softening components (A) and (B) wherein (A) is a biodegradable fatty ester quaternary ammonium compound of formula (I):
O +
R, (CH2)q O - C - R,
N X"
R (CH2)r - O - C - R,
(I)
O
wherein each R4 independently represents an aliphatic hydrocarbon group having from 8 to 22 carbon atoms,
R5 represents (CH2)SΓÇö R7 where R7 represents an alkoxy carbonyl group containing from 8 to 22 carbon atoms, benzyl, phenyl,
(CrC4) - alkyl substituted phenyl, OH or H; R6 represents (CH2)t R8 where R8 represents benzyl, phenyl, (CrC4) alkyl substituted phenyl, OH or H; q, r, s and t, each independently, represent a number of from 1 to 3; and x is an anion of valence a; and (B) is glycerol monostearate;
(b) an effective amount of an emulsifier comprising a fatty alcohol ethoxylate nonionic surfactant having a hydrophilic-lipophilic balance (HLB) value greater than about 7.5 as measured by the Davies Group Number Method; and
(c) an aqueous solvent, said fabric softener composition being free of an inorganic mineral acid and an organic acid.
12
2. A fabric softener composition in accordance with claim 1 wherein the fatty ester quaternary ammonium compound (A) is of the formula (II):
O CH2CH2OH O
R4-C-O (CH2)2 N+ (CH2)2 O-C-R, CH3SO4 "
(II)
CH,
3. A fabric softener composition in accordance with claim 2 wherein the diester quaternary ammonium compound is N-methyl-N,N,N-triethanolamine ditallowester quaternary ammonium methosulfate.
4. A fabric softener composition in accordance with claim 1 wherein said emulsifier is an ethoxylated C13-C15 fatty alcohol with 20 moles of ethoxylation per mole of alcohol.
5. A fabric softener composition in accordance with claim 1 wherein the amount of component (A) in the composition is from about 1% to about 20%, by weight, and the amount of component (B) is from about 0.1% to about 8%, by weight.
6. A method of imparting softness to fabrics comprising contacting the fabrics with an effective amount of the fabric softener composition of claim 1.
7. The method of claim 6 wherein said fabrics are contacted during the rinse cycle of an automatic laundry washing machine.
8. The method of claim 6 wherein said fabrics are contacted during a hand wash or rinse.
13
PCT/US1999/003378 1998-02-19 1999-02-17 Stable rinse cycle fabric softener composition with glycerol monostearate co-softener WO1999042547A1 (en)

Priority Applications (10)

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IL13233299A IL132332A (en) 1998-02-19 1999-02-17 Stable rinse cycle fabric softener composition with glycerol monostearate co-softener
CA002287514A CA2287514A1 (en) 1998-02-19 1999-02-17 Stable rinse cycle fabric softener composition with glycerol monostearate co-softener
AU27692/99A AU2769299A (en) 1998-02-19 1999-02-17 Stable rinse cycle fabric softener composition with glycerol monostearate co-softener
JP54267899A JP2001525020A (en) 1998-02-19 1999-02-17 Stable rinse cycle fabric softener composition comprising glycerol monostearate assisted softener
SK1549-99A SK154999A3 (en) 1998-02-19 1999-02-17 Stable rinse cycle fabric softener composition with glycerol monostearate co-softener
NZ500399A NZ500399A (en) 1998-02-19 1999-02-17 Stable rinse cycle fabric softener composition with glycerol monostearate co-softener
BR9904829-9A BR9904829A (en) 1998-02-19 1999-02-17 Fabric softener composition, dispersible in water, pourable and stable, and softening process to fabrics.
EP99908200A EP0975726A1 (en) 1998-02-19 1999-02-17 Stable rinse cycle fabric softener composition with glycerol monostearate co-softener
HU0003822A HUP0003822A3 (en) 1998-02-19 1999-02-17 Stable rinse cycle fabric softener composition with glycerol monostearate co-softener
BG103896A BG103896A (en) 1998-02-19 1999-11-16 Stable softening compositions for rinsing of fabrics with glycerol monostearate cosofteners

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US2619498A 1998-02-19 1998-02-19
US09/026,194 1998-02-19
US7045398A 1998-04-30 1998-04-30
US09/070,453 1998-04-30
US09/237,528 1999-01-27
US09/237,528 US6057285A (en) 1998-02-19 1999-01-27 Stable rinse cycle fabric softener composition with GMS co-softener

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WO2001002522A2 (en) * 1999-07-02 2001-01-11 The Dow Chemical Company Clear softening formulations including alkoxylated additives
KR100386420B1 (en) * 2000-12-20 2003-06-02 주식회사 엘지생활건강 Fabric softner composition
WO2003097776A1 (en) * 2002-05-16 2003-11-27 The Procter & Gamble Company Fabric conditioning composition comprising agent for enhancing the appearance of the rinse solution
WO2003097781A1 (en) * 2002-05-16 2003-11-27 The Procter & Gamble Company Rinse-added fabric treatment composition and methods and uses thereof
US6844311B2 (en) 2001-07-27 2005-01-18 Unilever Home & Personal Care Usa Division Of Conopco, Inc. Fabric conditioning compositions
WO2006133791A2 (en) * 2005-06-17 2006-12-21 Unilever Plc Fabric conditioning composition and use
US7163783B2 (en) * 2001-08-23 2007-01-16 Fuji Photo Film Co., Ltd. Rinse-processing composition for processing silver halide color photographic material, processing apparatus and processing method
EP2576743B1 (en) 2010-05-28 2015-11-11 Colgate-Palmolive Company Fatty acid chain saturation in alkanol amine based esterquat

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US6887243B2 (en) 2001-03-30 2005-05-03 Triage Medical, Inc. Method and apparatus for bone fixation with secondary compression
CN102036623A (en) 2008-04-05 2011-04-27 斯恩蒂斯有限公司 Expandable intervertebral implant
JP5479691B2 (en) * 2008-06-16 2014-04-23 花王株式会社 Liquid detergent composition
JP5281388B2 (en) * 2008-12-25 2013-09-04 花王株式会社 Liquid detergent composition
US8603961B2 (en) * 2010-12-01 2013-12-10 The Procter & Gamble Company Method of making a fabric care composition
CN109208328B (en) * 2017-07-07 2021-10-22 广州蓝月亮实业有限公司 Aqueous fabric softening composition
WO2021069249A1 (en) * 2019-10-07 2021-04-15 Unilever Ip Holdings B.V. Fabric softener

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US5747108A (en) * 1997-03-19 1998-05-05 Colgate-Palmolive Co. Super-concentrated liquid rinse cycle fabric softening composition

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EP0691396A2 (en) * 1994-06-09 1996-01-10 Hoechst Aktiengesellschaft Concentrated laundry softener
DE19623764A1 (en) * 1996-06-14 1997-12-18 Henkel Kgaa Aqueous fabric softener with high zeta potential
US5747108A (en) * 1997-03-19 1998-05-05 Colgate-Palmolive Co. Super-concentrated liquid rinse cycle fabric softening composition

Cited By (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2001002522A2 (en) * 1999-07-02 2001-01-11 The Dow Chemical Company Clear softening formulations including alkoxylated additives
WO2001002522A3 (en) * 1999-07-02 2002-09-26 Dow Chemical Co Clear softening formulations including alkoxylated additives
KR100386420B1 (en) * 2000-12-20 2003-06-02 주식회사 엘지생활건강 Fabric softner composition
US6844311B2 (en) 2001-07-27 2005-01-18 Unilever Home & Personal Care Usa Division Of Conopco, Inc. Fabric conditioning compositions
US7163783B2 (en) * 2001-08-23 2007-01-16 Fuji Photo Film Co., Ltd. Rinse-processing composition for processing silver halide color photographic material, processing apparatus and processing method
WO2003097776A1 (en) * 2002-05-16 2003-11-27 The Procter & Gamble Company Fabric conditioning composition comprising agent for enhancing the appearance of the rinse solution
WO2003097781A1 (en) * 2002-05-16 2003-11-27 The Procter & Gamble Company Rinse-added fabric treatment composition and methods and uses thereof
US7018977B2 (en) 2002-05-16 2006-03-28 The Procter & Gamble Company Rinse-added fabric treatment composition, product containing same and methods thereof
WO2006133791A2 (en) * 2005-06-17 2006-12-21 Unilever Plc Fabric conditioning composition and use
WO2006133791A3 (en) * 2005-06-17 2007-04-05 Unilever Plc Fabric conditioning composition and use
EP2576743B1 (en) 2010-05-28 2015-11-11 Colgate-Palmolive Company Fatty acid chain saturation in alkanol amine based esterquat

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HUP0003822A3 (en) 2003-02-28
IL132332A (en) 2003-02-12
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BR9904829A (en) 2000-05-23
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TR199902595T1 (en) 2000-10-23
CN1258313A (en) 2000-06-28

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