EP0443313B1 - Liquid softener composition for fabric - Google Patents
Liquid softener composition for fabric Download PDFInfo
- Publication number
- EP0443313B1 EP0443313B1 EP19910100210 EP91100210A EP0443313B1 EP 0443313 B1 EP0443313 B1 EP 0443313B1 EP 19910100210 EP19910100210 EP 19910100210 EP 91100210 A EP91100210 A EP 91100210A EP 0443313 B1 EP0443313 B1 EP 0443313B1
- Authority
- EP
- European Patent Office
- Prior art keywords
- carbon atoms
- acid
- composition
- alkyl
- formula
- 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.)
- Expired - Lifetime
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- 239000000203 mixture Substances 0.000 title claims description 32
- 239000007788 liquid Substances 0.000 title claims description 10
- 239000004744 fabric Substances 0.000 title 1
- 125000004432 carbon atom Chemical group C* 0.000 claims description 32
- 125000000217 alkyl group Chemical group 0.000 claims description 25
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 20
- -1 ester amine Chemical class 0.000 claims description 19
- 150000003242 quaternary ammonium salts Chemical class 0.000 claims description 13
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims description 10
- 125000003342 alkenyl group Chemical group 0.000 claims description 7
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 6
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims description 6
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 claims description 6
- 125000001183 hydrocarbyl group Chemical group 0.000 claims description 6
- 229920006395 saturated elastomer Polymers 0.000 claims description 6
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 claims description 5
- AEMRFAOFKBGASW-UHFFFAOYSA-N Glycolic acid Chemical compound OCC(O)=O AEMRFAOFKBGASW-UHFFFAOYSA-N 0.000 claims description 5
- 239000001110 calcium chloride Substances 0.000 claims description 5
- 229910001628 calcium chloride Inorganic materials 0.000 claims description 5
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 claims description 5
- 150000007522 mineralic acids Chemical class 0.000 claims description 5
- 150000007524 organic acids Chemical class 0.000 claims description 5
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 claims description 4
- TWRXJAOTZQYOKJ-UHFFFAOYSA-L Magnesium chloride Chemical compound [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 claims description 4
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 claims description 4
- 239000003792 electrolyte Substances 0.000 claims description 4
- JHJLBTNAGRQEKS-UHFFFAOYSA-M sodium bromide Chemical compound [Na+].[Br-] JHJLBTNAGRQEKS-UHFFFAOYSA-M 0.000 claims description 4
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 claims description 4
- LBLYYCQCTBFVLH-UHFFFAOYSA-N 2-Methylbenzenesulfonic acid Chemical compound CC1=CC=CC=C1S(O)(=O)=O LBLYYCQCTBFVLH-UHFFFAOYSA-N 0.000 claims description 3
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 3
- 229910052736 halogen Inorganic materials 0.000 claims description 3
- 125000002768 hydroxyalkyl group Chemical group 0.000 claims description 3
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 claims description 3
- GAWIXWVDTYZWAW-UHFFFAOYSA-N C[CH]O Chemical group C[CH]O GAWIXWVDTYZWAW-UHFFFAOYSA-N 0.000 claims description 2
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims description 2
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 claims description 2
- 239000001530 fumaric acid Substances 0.000 claims description 2
- 239000004310 lactic acid Substances 0.000 claims description 2
- 235000014655 lactic acid Nutrition 0.000 claims description 2
- 229910001629 magnesium chloride Inorganic materials 0.000 claims description 2
- 239000011976 maleic acid Substances 0.000 claims description 2
- 239000011780 sodium chloride Substances 0.000 claims description 2
- 125000005843 halogen group Chemical group 0.000 claims 1
- 150000001875 compounds Chemical class 0.000 description 14
- 239000003760 tallow Substances 0.000 description 9
- 230000000694 effects Effects 0.000 description 8
- 238000000034 method Methods 0.000 description 8
- 150000001412 amines Chemical class 0.000 description 6
- 235000014113 dietary fatty acids Nutrition 0.000 description 6
- 239000006185 dispersion Substances 0.000 description 6
- 238000011156 evaluation Methods 0.000 description 6
- 239000000194 fatty acid Substances 0.000 description 6
- 229930195729 fatty acid Natural products 0.000 description 6
- 150000004665 fatty acids Chemical class 0.000 description 5
- 238000003756 stirring Methods 0.000 description 5
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 4
- 235000011148 calcium chloride Nutrition 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
- 239000000835 fiber Substances 0.000 description 4
- 239000002245 particle Substances 0.000 description 4
- 229920001296 polysiloxane Polymers 0.000 description 4
- 238000003786 synthesis reaction Methods 0.000 description 4
- 229920000742 Cotton Polymers 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- 150000003973 alkyl amines Chemical class 0.000 description 3
- 239000007864 aqueous solution Substances 0.000 description 3
- IPTLKMXBROVJJF-UHFFFAOYSA-N azanium;methyl sulfate Chemical compound N.COS(O)(=O)=O IPTLKMXBROVJJF-UHFFFAOYSA-N 0.000 description 3
- 230000003750 conditioning effect Effects 0.000 description 3
- CRVGTESFCCXCTH-UHFFFAOYSA-N methyl diethanolamine Chemical compound OCCN(C)CCO CRVGTESFCCXCTH-UHFFFAOYSA-N 0.000 description 3
- 230000003472 neutralizing effect Effects 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- 238000005406 washing Methods 0.000 description 3
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 2
- HPEUJPJOZXNMSJ-UHFFFAOYSA-N Methyl stearate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OC HPEUJPJOZXNMSJ-UHFFFAOYSA-N 0.000 description 2
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 125000005263 alkylenediamine group Chemical group 0.000 description 2
- 235000015278 beef Nutrition 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 150000002367 halogens Chemical group 0.000 description 2
- JZMJDSHXVKJFKW-UHFFFAOYSA-M methyl sulfate(1-) Chemical compound COS([O-])(=O)=O JZMJDSHXVKJFKW-UHFFFAOYSA-M 0.000 description 2
- 125000001453 quaternary ammonium group Chemical group 0.000 description 2
- 239000008237 rinsing water Substances 0.000 description 2
- 239000004753 textile Substances 0.000 description 2
- NKFNBVMJTSYZDV-UHFFFAOYSA-N 2-[dodecyl(2-hydroxyethyl)amino]ethanol Chemical compound CCCCCCCCCCCCN(CCO)CCO NKFNBVMJTSYZDV-UHFFFAOYSA-N 0.000 description 1
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 description 1
- KRGXWTOLFOPIKV-UHFFFAOYSA-N 3-(methylamino)propan-1-ol Chemical compound CNCCCO KRGXWTOLFOPIKV-UHFFFAOYSA-N 0.000 description 1
- IYAQFFOKAFGDKE-UHFFFAOYSA-N 4,5-dihydro-1h-imidazol-3-ium;methyl sulfate Chemical compound C1CN=CN1.COS(O)(=O)=O IYAQFFOKAFGDKE-UHFFFAOYSA-N 0.000 description 1
- QISOBCMNUJQOJU-UHFFFAOYSA-N 4-bromo-1h-pyrazole-5-carboxylic acid Chemical compound OC(=O)C=1NN=CC=1Br QISOBCMNUJQOJU-UHFFFAOYSA-N 0.000 description 1
- CNGYZEMWVAWWOB-VAWYXSNFSA-N 5-[[4-anilino-6-[bis(2-hydroxyethyl)amino]-1,3,5-triazin-2-yl]amino]-2-[(e)-2-[4-[[4-anilino-6-[bis(2-hydroxyethyl)amino]-1,3,5-triazin-2-yl]amino]-2-sulfophenyl]ethenyl]benzenesulfonic acid Chemical compound N=1C(NC=2C=C(C(\C=C\C=3C(=CC(NC=4N=C(N=C(NC=5C=CC=CC=5)N=4)N(CCO)CCO)=CC=3)S(O)(=O)=O)=CC=2)S(O)(=O)=O)=NC(N(CCO)CCO)=NC=1NC1=CC=CC=C1 CNGYZEMWVAWWOB-VAWYXSNFSA-N 0.000 description 1
- PXRKCOCTEMYUEG-UHFFFAOYSA-N 5-aminoisoindole-1,3-dione Chemical compound NC1=CC=C2C(=O)NC(=O)C2=C1 PXRKCOCTEMYUEG-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- 235000019482 Palm oil Nutrition 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- 235000019484 Rapeseed oil Nutrition 0.000 description 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 235000019270 ammonium chloride Nutrition 0.000 description 1
- 239000003945 anionic surfactant Substances 0.000 description 1
- 239000002216 antistatic agent Substances 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000003240 coconut oil Substances 0.000 description 1
- 235000019864 coconut oil Nutrition 0.000 description 1
- 239000003599 detergent Substances 0.000 description 1
- VKKVMDHHSINGTJ-UHFFFAOYSA-M di(docosyl)-dimethylazanium;chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCCCCCCCC[N+](C)(C)CCCCCCCCCCCCCCCCCCCCCC VKKVMDHHSINGTJ-UHFFFAOYSA-M 0.000 description 1
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 1
- 239000004205 dimethyl polysiloxane Substances 0.000 description 1
- UAKOZKUVZRMOFN-JDVCJPALSA-M dimethyl-bis[(z)-octadec-9-enyl]azanium;chloride Chemical compound [Cl-].CCCCCCCC\C=C/CCCCCCCC[N+](C)(C)CCCCCCCC\C=C/CCCCCCCC UAKOZKUVZRMOFN-JDVCJPALSA-M 0.000 description 1
- IQDGSYLLQPDQDV-UHFFFAOYSA-N dimethylazanium;chloride Chemical compound Cl.CNC IQDGSYLLQPDQDV-UHFFFAOYSA-N 0.000 description 1
- REZZEXDLIUJMMS-UHFFFAOYSA-M dimethyldioctadecylammonium chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCCCC[N+](C)(C)CCCCCCCCCCCCCCCCCC REZZEXDLIUJMMS-UHFFFAOYSA-M 0.000 description 1
- 239000004664 distearyldimethylammonium chloride (DHTDMAC) Substances 0.000 description 1
- CAMHHLOGFDZBBG-UHFFFAOYSA-N epoxidized methyl oleate Natural products CCCCCCCCC1OC1CCCCCCCC(=O)OC CAMHHLOGFDZBBG-UHFFFAOYSA-N 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 239000002657 fibrous material Substances 0.000 description 1
- 229940013317 fish oils Drugs 0.000 description 1
- 239000000796 flavoring agent Substances 0.000 description 1
- 235000019634 flavors Nutrition 0.000 description 1
- 239000008233 hard water Substances 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 238000011835 investigation Methods 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 150000004702 methyl esters Chemical class 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- 235000014593 oils and fats Nutrition 0.000 description 1
- 239000002540 palm oil Substances 0.000 description 1
- 239000002304 perfume Substances 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 description 1
- 229920000151 polyglycol Polymers 0.000 description 1
- 239000010695 polyglycol Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 150000003856 quaternary ammonium compounds Chemical class 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 238000010008 shearing Methods 0.000 description 1
- 239000008234 soft water Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
Classifications
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
- D06M13/322—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing nitrogen
- D06M13/46—Compounds containing quaternary nitrogen atoms
- D06M13/47—Compounds containing quaternary nitrogen atoms derived from heterocyclic compounds
- D06M13/473—Compounds containing quaternary nitrogen atoms derived from heterocyclic compounds having five-membered heterocyclic rings
-
- 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
- C11D1/40—Monoamines or polyamines; Salts thereof
-
- 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
- C11D3/0005—Other compounding ingredients characterised by their effect
- C11D3/001—Softening compositions
- C11D3/0015—Softening compositions liquid
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
- D06M13/322—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing nitrogen
- D06M13/46—Compounds containing quaternary nitrogen atoms
- D06M13/463—Compounds containing quaternary nitrogen atoms derived from monoamines
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M2200/00—Functionality of the treatment composition and/or properties imparted to the textile material
- D06M2200/50—Modified hand or grip properties; Softening compositions
Definitions
- the present invention relates to a liquid softener.
- the present invention relates to a household liquid softener capable of imparting an excellent softness to various fibers and having an excellent dispersibility in rinsing water.
- compositions mainly comprising a quaternary ammonium salt having 1 or 2 long-chain alkyl groups in the molecule such as di(hardened tallow alkyl)-dimethylammonium chloride, since the quaternary ammonium salt used even in a small amount exhibits an excellent softening effect on various fibers.
- the softeners comprising the quaternary ammonium salt as the main base are put on the market and used usually in the form of 4 to 20% dispersion.
- liquid softeners comprising an amine as the softening base have been heretofore known.
- Japanese Patent Laid-Open No. 59796/1977 discloses a composition for softening fibers which comprises a long-chain alkylamine such as methyldi(hardened tallow alkyl)amine; JP-A 55-45898 (1980) shoes that a condensate of an aliphatic acid and an alkanolamine is neutralized or quaternarized by addition of an amideamine compound to liquidify and use it as its aqueous solution.
- JP-A 58-60070(1983) discloses a softener for fibrous materials which comprises an acylated alkanolamine, a water-soluble quaternary ammonium salt and a fatty acid ester and which imparts a lubricity and a pleasant touch to the fibers;
- Japanese Patent Laid-Open No. 167083/1986 discloses a highly dispersible softener comprising a quaternary ammonium compound, a condensate of a higher fatty acid with a hydroxylated lower alkylpolyamine and an alkylamine polyglycol ether; Japanese Patent Laid-Open No.
- 275474/1986 discloses a stable aqueous dispersion for treating textiles which comprises a di(higher alkyl)cyclic amine and a Brönstedt acid
- Japanese Patent Laid-Open No. 85368/1989 discloses a softening composition comprising a di(long-chain alkyl)amine / anionic surfactant ion pair complex, a non-silicone wax and a liquid carrier
- composition for conditioning cloths which comprises a condensate of an amine such as a hydroxylated (lower alkyl) alkylenediamine with a higher fatty acid and an amphoteric conditioning agent for cloths; and Japanese Patent Laid-Open No. 14076/1990 discloses a composition for conditioning cloths which comprises a di(long chain)alkylamine / polyfunctional carboxylic acid complex and which is capable of imparting softness and antistatic properties to the cloths.
- an amine such as a hydroxylated (lower alkyl) alkylenediamine with a higher fatty acid and an amphoteric conditioning agent for cloths
- Japanese Patent Laid-Open No. 14076/1990 discloses a composition for conditioning cloths which comprises a di(long chain)alkylamine / polyfunctional carboxylic acid complex and which is capable of imparting softness and antistatic properties to the cloths.
- Japanese Patent Laid-Open No. 5394/1977 discloses a composition for regulating the conditions of cloths which comprises a mono- or di(long chain alkyl)alkylenediamine antistatic agent and a quaternary ammonium softener.
- the liquid softener composition is useful for the housework, improved in softening and rinsing and comprises (a) 10 to 30 percent by weight of a neutralized product of an inorganic or organic acid with an ester amine having the formula (I) or (VII), having an average size of 0.1 to 5 ⁇ m in the dispersed state, (b) 0.2 to 10 percent by weight of an inorganic electrolyte and the balance of water.
- R1 and R2 each are a hydrocarbon group having 11 to 23 carbon atoms, straight or branched, saturated or unsaturated
- R is a hydrocarbon group having 1 to 24 carbon atoms, straight or branched, saturated or unsaturated, hydroxyethyl, hydroxypropyl
- R10 is a hydrocarbon group having 8 to 24 carbon atoms, straight or branched, saturated or unsaturated
- m is 2 or 3.
- composition may further comprise (c) a water-insoluble quaternary ammonium salt having one of the formulae (II), (IV), (V) and (VI) at a weight ratio of (a) to (c) in the range between 95/5 and 50/50.
- a water-insoluble quaternary ammonium salt having one of the formulae (II), (IV), (V) and (VI) at a weight ratio of (a) to (c) in the range between 95/5 and 50/50.
- R3, R4, R8 and R9 are each an alkyl having 10 to 24 carbon atoms, an alkenyl having 10 to 24 carbon atoms, a beta-hydroxyalkyl having 10 to 24 carbon atoms
- R5 and R6 are each an alkyl having 1 to 3 carbon atoms, hydroxyalkyl having 1 to 3 carbon atoms, benzyl or -(C2H4O)q-H, q being 1 to 3
- X is a halogen or a monoalkyl sulfate having 1 to 3 carbon atoms in the alkyl.
- the invention includes two embodiments, one in which the ester amine (a) has the formula (I) and the other in which the ester amine (a) has the formula (VII).
- the inorganic acid for (a) is hydrochloric acid or sulfuric acid and the organic acid is acetic acid, glycolic acid, lactic acid, citric acid, maleic acid, fumaric acid or toluenesulfonic acid.
- R1 and R2 each are an alkyl having 15 to 23 carbon atoms or an alkenyl having 15 to 23 carbon atoms and R is an alkyl having 1 to 3 carbon atoms.
- ester amine for (a) has the formula (VII)
- one of R1 and R10 has 16 or more carbon atoms.
- the inorganic electrolyte is selected from the group consisting of sodium chloride, sodium bromide, calcium chloride and magnesium chloride.
- the compound having the formulae (I) or (VII) preferably includes those obtained by reacting an alkanolamine such as N-long chain alkyl-dipropanolamine, triethanolamine, tripropanolamine, N-methyldiethanolamine, N-methylpropanolamine or an N-(long-chain alkyl)diethanolamine with a fatty acid having 12 to 24 carbon atoms or methyl ester thereof and neutralizing the reaction product with an inorganic acid such as hydrochloric or sulfuric acid or an organic acid such as acetic, glycolic, lactic, citric, maleic, fumaric or toluenesulfonic acid.
- the fatty acids used in the reaction are usually those produced from natural oils and fats such as coconut oil, palm oil, beef tallow, rapeseed oil and fish oils. Further, chemically synthesized fatty acids are also usable.
- the most desirable components (a) are neutralized amine compounds of the general formula (I) wherein R1 and R2 each represent an alkyl or alkenyl group having at least 15 carbon atoms and R represents an alkyl group having 1 to 3 carbon atoms.
- the liquid softener composition comprises 10 to 30 wt.%, preferably 10 to 25 wt.% of (a), 0.2 to 10 wt.%, preferably 0.4 to 5 wt.%, more preferably 0.6 to 5 wt.%, based on the weight of (a), of (b) and the balance of water.
- composition of the present invention is obtained by, for example, slowly adding a melt of the amine compound or a concentrated solution thereof into an aqueous solution of the neutralizing agent under stirring or shear stirring.
- process for producing the composition of the present invention is not limited to this and other processes wherein the neutralized product is previously produced or the neutralizing agent is added afterward can also be employed.
- the preferred mean particle diameter of the component (a) is in the range of 0.1 to 5 ⁇ m.
- the most desirable method of adjusting the mean particle diameter in this range comprises varying the stirring shearing force depending on the kind and amount of the component (a) in the incorporation step.
- the mean particle diameter of the component (a) is less than 0.1 ⁇ m, the softness is reduced and, on the contrary, when it exceeds 5 ⁇ m, the dispersibility thereof in water is reduced.
- a preferable size of (a) ranges from 0.5 to 3 ⁇ m.
- the liquid softener of the present invention may contain an ordinary quaternary ammonium salt.
- the quaternary ammonium salts are, for example, as follows: wherein R3, R4, R8 and R9 each represent an alkyl, alkenyl or ⁇ -hydroxyalkyl group having 10 to 24 carbon atoms, R5 and R6 each represent an alkyl or hydroxyalkyl group having 1 to 3 carbon atoms, a benzyl group or -(C2H4O) q -H, wherein q represents 1 to 3, and X represents a halogen or a monoalkylsulfate group having an alkyl group having 1 to 3 carbon atoms.
- Examples of the compounds of the general formula (II) include ditallowdimethylammonium chloride, ditallowdimethylammonium methyl sulfate, di(hydrogenated tallow)dimethylammonium chloride, distearyldimethylammonium chloride, dibehenyldimethylammonium chloride and dioleyldimethylammonium chloride.
- Examples of the compounds of the general formula (IV) include 1-methyl-1-tallowamidoethyl-2-tallowimidazolinium methyl sulfate and 1-methyl-1-(hydrogenated tallow tallow amidoethyl)imidazolinium methyl sulfate.
- Examples of the compounds of the general formula (V) include methylbis(tallowyloxyethyl) 2-hydroxyethyl) ammonium chloride and methylbis-(stearoyloxyethyl)(2-hydroxethyl)ammonium methyl sulfate.
- Examples of the compounds of the general formula (VI) include methylbis(tallow amidoethyl)-(2-hydroxyethyl)ammonium methyl sulfate and methylbis(hydrogenated tallow amidoethyl)-(2-hydroxyethyl)ammonium methyl sulfate.
- the weight ratio of the component (a) to the quaternary ammonium salt is in the range of 95/5 to 50/50, preferably 90/10 to 60/40.
- the total weight of the component (a) and quaternary ammonium salt in the composition is preferably 10 to 30% by weight.
- the composition preferably has a pH of 3 to 6.
- the liquid softener of the present invention may contain a nonionic surfactant such as a polyoxyethylene(5 to 50 mol)alkyl or alkenyl(C12 to C24) ether for improving the storage stability; a solvent such as ethanol, propylene glycol or ethylene glycol; urea; a silicone such as polydimethylsiloxane, polyether-modified silicone or amino-modified silicone for improving the water absorption; a pigment or dye for improving the appearance of the product; fluorescent brightener for increasing the whiteness of the softened clothes; and a flavor for a favorable feeling during the use or after the finish.
- a nonionic surfactant such as a polyoxyethylene(5 to 50 mol)alkyl or alkenyl(C12 to C24) ether for improving the storage stability
- a solvent such as ethanol, propylene glycol or ethylene glycol
- urea a silicone such as polydimethylsiloxane, polyether-modified silicone or amino-mod
- the cloths treated as described above were air-dried in a room and then left to stand in an air-conditioned room at 25°C and 65% RH for 24 h.
- the softness was evaluated by the paired comparison method with the cloths which had been treated with 20 ml of a softener comprising 15% by weight of di(hydrogenated tallow alkyl)-dimethylammonium chloride as the control.
- the results were classified into the following groups:
- the amount of the component (a) in the composition was 15% by weight.
- the height of a cotton towel pile was determined for evaluating the resilience thereof treated with a 15% dispersion (containing 0.1% of CaCl2) of each of the compositions listed in Table 6.
- Cotton towels treated in the same manner as that of Examples 14 to 26 were folded in eight, and three towels thus folded were piled. A pressure of 5 g/cm2 was applied thereto for 5 min and taken away, and the height of the pile was determined. The higher the pile, the higher the resilience.
- compositions listed in Table 7 were evaluated in view of the softening effect and dispersibility in water by the same method as in the Examples 1. Results are shown in Table 8. It is noted from Table 8 that when the compound of the present invention is used, both satisfactory softness and water dispersibility can be obtained.
- composition was prepared and evaluated in the same manner as in Example 1, except that the composition comprised 12 wt.% of (a'-1), 3 wt.% of di-hardened beef tallow-dimethylammonium chloride, 0.15 wt.% of CaCl2, 0.3 wt.% of perfume and the balance of water and the mean particle diameter thereof was 1.0 ⁇ m.
- the softness and the water dispersibility were found to be +1 and +2, respectively.
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- Engineering & Computer Science (AREA)
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- Life Sciences & Earth Sciences (AREA)
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- Oil, Petroleum & Natural Gas (AREA)
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Description
- The present invention relates to a liquid softener. In particular, the present invention relates to a household liquid softener capable of imparting an excellent softness to various fibers and having an excellent dispersibility in rinsing water.
- Most of household softeners now available on-the market are compositions mainly comprising a quaternary ammonium salt having 1 or 2 long-chain alkyl groups in the molecule such as di(hardened tallow alkyl)-dimethylammonium chloride, since the quaternary ammonium salt used even in a small amount exhibits an excellent softening effect on various fibers.
- The softeners comprising the quaternary ammonium salt as the main base are put on the market and used usually in the form of 4 to 20% dispersion.
- When the quaternary ammonium having a strong hydrophobic property is added to water and the stirring power is weak, the dispersibility thereof in water is poor and, therefore, it cannot be evenly applied to the clothes. Although commercially available softeners contain various additives in addition to the quaternary ammonium salt to improve the dispersibility thereof in water, the effects of them are yet insufficient.
- Further, liquid softeners comprising an amine as the softening base have been heretofore known. For example, Japanese Patent Laid-Open No. 59796/1977 discloses a composition for softening fibers which comprises a long-chain alkylamine such as methyldi(hardened tallow alkyl)amine; JP-A 55-45898 (1980) shoes that a condensate of an aliphatic acid and an alkanolamine is neutralized or quaternarized by addition of an amideamine compound to liquidify and use it as its aqueous solution. JP-A 58-60070(1983) discloses a softener for fibrous materials which comprises an acylated alkanolamine, a water-soluble quaternary ammonium salt and a fatty acid ester and which imparts a lubricity and a pleasant touch to the fibers; Japanese Patent Laid-Open No. 167083/1986 discloses a highly dispersible softener comprising a quaternary ammonium compound, a condensate of a higher fatty acid with a hydroxylated lower alkylpolyamine and an alkylamine polyglycol ether; Japanese Patent Laid-Open No. 275474/1986 discloses a stable aqueous dispersion for treating textiles which comprises a di(higher alkyl)cyclic amine and a Brönstedt acid; Japanese Patent Laid-Open No. 85368/1989 discloses a softening composition comprising a di(long-chain alkyl)amine / anionic surfactant ion pair complex, a non-silicone wax and a liquid carrier; Japanese Patent Laid-Open No. 6662/1990 discloses a composition for conditioning cloths which comprises a condensate of an amine such as a hydroxylated (lower alkyl) alkylenediamine with a higher fatty acid and an amphoteric conditioning agent for cloths; and Japanese Patent Laid-Open No. 14076/1990 discloses a composition for conditioning cloths which comprises a di(long chain)alkylamine / polyfunctional carboxylic acid complex and which is capable of imparting softness and antistatic properties to the cloths.
- Further, Japanese Patent Laid-Open No. 5394/1977 discloses a composition for regulating the conditions of cloths which comprises a mono- or di(long chain alkyl)alkylenediamine antistatic agent and a quaternary ammonium softener.
- However, the effects of the amine-containing softeners are yet insufficient.
- After intensive investigations of amine-containing softeners, the inventors have found that a neutralized salt of a specified ester amine compound has an excellent softening effect and a quite high dispersibility in rinsing water. The present invention has been completed on the basis of this finding.
- The liquid softener composition is useful for the housework, improved in softening and rinsing and comprises (a) 10 to 30 percent by weight of a neutralized product of an inorganic or organic acid with an ester amine having the formula (I) or (VII), having an average size of 0.1 to 5 µm in the dispersed state, (b) 0.2 to 10 percent by weight of an inorganic electrolyte and the balance of water.
in which R1 and R2 each are a hydrocarbon group having 11 to 23 carbon atoms, straight or branched, saturated or unsaturated, R is a hydrocarbon group having 1 to 24 carbon atoms, straight or branched, saturated or unsaturated, hydroxyethyl, hydroxypropyl, R10 is a hydrocarbon group having 8 to 24 carbon atoms, straight or branched, saturated or unsaturated, and m is 2 or 3. - The composition may further comprise (c) a water-insoluble quaternary ammonium salt having one of the formulae (II), (IV), (V) and (VI) at a weight ratio of (a) to (c) in the range between 95/5 and 50/50.
in which R3, R4, R8 and R9 are each an alkyl having 10 to 24 carbon atoms, an alkenyl having 10 to 24 carbon atoms, a beta-hydroxyalkyl having 10 to 24 carbon atoms, R5 and R6 are each an alkyl having 1 to 3 carbon atoms, hydroxyalkyl having 1 to 3 carbon atoms, benzyl or -(C2H4O)q-H, q being 1 to 3, X is a halogen or a monoalkyl sulfate having 1 to 3 carbon atoms in the alkyl. - The invention includes two embodiments, one in which the ester amine (a) has the formula (I) and the other in which the ester amine (a) has the formula (VII).
- It is preferably that the inorganic acid for (a) is hydrochloric acid or sulfuric acid and the organic acid is acetic acid, glycolic acid, lactic acid, citric acid, maleic acid, fumaric acid or toluenesulfonic acid.
- When the ester amine for (a) has the formula (I), R1 and R2 each are an alkyl having 15 to 23 carbon atoms or an alkenyl having 15 to 23 carbon atoms and R is an alkyl having 1 to 3 carbon atoms.
- When the ester amine for (a) has the formula (VII), one of R1 and R10 has 16 or more carbon atoms.
- It is preferable that the inorganic electrolyte is selected from the group consisting of sodium chloride, sodium bromide, calcium chloride and magnesium chloride.
- The compound having the formulae (I) or (VII) preferably includes those obtained by reacting an alkanolamine such as N-long chain alkyl-dipropanolamine, triethanolamine, tripropanolamine, N-methyldiethanolamine, N-methylpropanolamine or an N-(long-chain alkyl)diethanolamine with a fatty acid having 12 to 24 carbon atoms or methyl ester thereof and neutralizing the reaction product with an inorganic acid such as hydrochloric or sulfuric acid or an organic acid such as acetic, glycolic, lactic, citric, maleic, fumaric or toluenesulfonic acid. The fatty acids used in the reaction are usually those produced from natural oils and fats such as coconut oil, palm oil, beef tallow, rapeseed oil and fish oils. Further, chemically synthesized fatty acids are also usable.
- The most desirable components (a) are neutralized amine compounds of the general formula (I) wherein R₁ and R₂ each represent an alkyl or alkenyl group having at least 15 carbon atoms and R represents an alkyl group having 1 to 3 carbon atoms.
- The liquid softener composition comprises 10 to 30 wt.%, preferably 10 to 25 wt.% of (a), 0.2 to 10 wt.%, preferably 0.4 to 5 wt.%, more preferably 0.6 to 5 wt.%, based on the weight of (a), of (b) and the balance of water.
- The composition of the present invention is obtained by, for example, slowly adding a melt of the amine compound or a concentrated solution thereof into an aqueous solution of the neutralizing agent under stirring or shear stirring. However, the process for producing the composition of the present invention is not limited to this and other processes wherein the neutralized product is previously produced or the neutralizing agent is added afterward can also be employed.
- From the viewpoints of the dispersibility in water and softening effect, the preferred mean particle diameter of the component (a) is in the range of 0.1 to 5 µm. The most desirable method of adjusting the mean particle diameter in this range comprises varying the stirring shearing force depending on the kind and amount of the component (a) in the incorporation step. When the mean particle diameter of the component (a) is less than 0.1 µm, the softness is reduced and, on the contrary, when it exceeds 5 µm, the dispersibility thereof in water is reduced. A preferable size of (a) ranges from 0.5 to 3 µm.
- The liquid softener of the present invention may contain an ordinary quaternary ammonium salt. The quaternary ammonium salts are, for example, as follows:
wherein R³, R⁴, R⁸ and R⁹ each represent an alkyl, alkenyl or β-hydroxyalkyl group having 10 to 24 carbon atoms, R⁵ and R⁶ each represent an alkyl or hydroxyalkyl group having 1 to 3 carbon atoms, a benzyl group or -(C₂H₄O)q-H, wherein q represents 1 to 3, and X represents a halogen or a monoalkylsulfate group having an alkyl group having 1 to 3 carbon atoms. - Examples of the compounds of the general formula (II) include ditallowdimethylammonium chloride, ditallowdimethylammonium methyl sulfate, di(hydrogenated tallow)dimethylammonium chloride, distearyldimethylammonium chloride, dibehenyldimethylammonium chloride and dioleyldimethylammonium chloride.
- Examples of the compounds of the general formula (IV) include 1-methyl-1-tallowamidoethyl-2-tallowimidazolinium methyl sulfate and 1-methyl-1-(hydrogenated tallow tallow amidoethyl)imidazolinium methyl sulfate.
- Examples of the compounds of the general formula (V) include methylbis(tallowyloxyethyl) 2-hydroxyethyl) ammonium chloride and methylbis-(stearoyloxyethyl)(2-hydroxethyl)ammonium methyl sulfate.
- Examples of the compounds of the general formula (VI) include methylbis(tallow amidoethyl)-(2-hydroxyethyl)ammonium methyl sulfate and methylbis(hydrogenated tallow amidoethyl)-(2-hydroxyethyl)ammonium methyl sulfate.
- With these quaternary ammonium salts, not only the softness but also a resilience (fluffiness) can be imparted to the clothes. The weight ratio of the component (a) to the quaternary ammonium salt is in the range of 95/5 to 50/50, preferably 90/10 to 60/40. The total weight of the component (a) and quaternary ammonium salt in the composition is preferably 10 to 30% by weight. The composition preferably has a pH of 3 to 6.
- The liquid softener of the present invention may contain a nonionic surfactant such as a polyoxyethylene(5 to 50 mol)alkyl or alkenyl(C₁₂ to C₂₄) ether for improving the storage stability; a solvent such as ethanol, propylene glycol or ethylene glycol; urea; a silicone such as polydimethylsiloxane, polyether-modified silicone or amino-modified silicone for improving the water absorption; a pigment or dye for improving the appearance of the product; fluorescent brightener for increasing the whiteness of the softened clothes; and a flavor for a favorable feeling during the use or after the finish.
- The following Examples will further illustrate the present invention, which by no means limit the invention.
- The following Synthesis Example will show the process for producing neutralized amidoamine compounds used in the present invention.
- 119 g of N-methyldiethanolamine were added to 596 g of methyl stearate and the reaction was conducted at 140 to 160°C for 3 h to obtain the esteramine.
- The condensate thus obtained was added to 500 g of a 12% aqueous solution of acetic acid to obtain compound (a-1) of the present invention.
-
- The softening effect and water dispersibility of each of the compositions listed in Table 2 were evaluated by the following methods:
-
- 2 kg of commercially available cotton towels and 1 kg of commercially available acrylic jersey cloths were washed with a commercially available detergent ('Attack': registered trade name of Kao Corporation) in 3.5° DH hard water with a 30-ℓ washing machine five times to remove textile treating agents from them. Then they were treated with 10 mℓ of a 15% dispersion of each of the compositions listed in Table 2 under stirring at 25°C for 1 min.
- The cloths treated as described above were air-dried in a room and then left to stand in an air-conditioned room at 25°C and 65% RH for 24 h.
- The softness of these cloths was examined.
- The softness was evaluated by the paired comparison method with the cloths which had been treated with 20 mℓ of a softener comprising 15% by weight of di(hydrogenated tallow alkyl)-dimethylammonium chloride as the control. The results were classified into the following groups:
- +2:
- softer than the control
- +1:
- slightly softer than the control
- 0:
- same as the control
- -1:
- the control was slightly softer
- -2:
- the control was softer.
- Water was poured up to a high water level into a fully automatic washing machine ('Shizuka Gozen for Bio 65' mfd. by Hitachi, Ltd.) and the washing machine was operated (soft water whirling) for 2 min. After 5 sec, each of the compositions listed in Table 2 was thrown into the water and the dispersibility thereof was examined after 5, 10 and 30 sec. The results were classified into the following groups:
- +2:
- homogeneously dispersed after 5 sec
- +1:
- homogeneously dispersed after 10 sec
- 0:
- homogeneously dispersed after 30 sec
- -1:
- the dispersion was partially heterogeneous after 30 sec
- -2:
- not dispersed at all even after 30 sec.
-
- The amount of the component (a) in the composition was 15% by weight.
- The softening properties and water dispersibility were evaluated in the same manner as that of Examples 1 to 13 except that each of the neutralized esteramines listed in Table 3, quaternary ammonium salts listed in Table 4 and a 15% dispersion (containing 0.1% of CaCl₂) of each of the compositions listed in Table 5 were used. The resilience was also evaluated in the evaluation of the softness.
- The resilience was evaluated according to the following criteria:
- +2:
- more resilient than the control,
- +1:
- slightly more resilient than the control,
- 0:
- similar to that of the control.
- -1:
- slightly less resilient than the control,
- -2:
- less resilient than the control.
- The height of a cotton towel pile was determined for evaluating the resilience thereof treated with a 15% dispersion (containing 0.1% of CaCl₂) of each of the compositions listed in Table 6.
-
- Compound (a'-1) of the present inventon was obtained in the same manner as in the preparation of compound (a-1) of Synthesis Example 1, except that 546 g of N-lauryldiethanolamine was used instead of 119 g of N-methyldiethanolamine. Compounds (a'-2) to (a'-5) of the present invention listed in Table 7 were prepared in the same manner as here.
- The compositions listed in Table 7 were evaluated in view of the softening effect and dispersibility in water by the same method as in the Examples 1. Results are shown in Table 8. It is noted from Table 8 that when the compound of the present invention is used, both satisfactory softness and water dispersibility can be obtained.
- The following composition was prepared and evaluated in the same manner as in Example 1, except that the composition comprised 12 wt.% of (a'-1), 3 wt.% of di-hardened beef tallow-dimethylammonium chloride, 0.15 wt.% of CaCl2, 0.3 wt.% of perfume and the balance of water and the mean particle diameter thereof was 1.0 µm. The softness and the water dispersibility were found to be +1 and +2, respectively. Evaluation in elasticity, made in the same manner as in Example 27, showed that the height of pile was 9.7 cm. When the composition of the Comarative Example 5 was used, the height of pile was found to be 8.8 cm.
Claims (8)
- A liquid softener composition comprising (a) 10 to 30 percent by weight of a neutralized product of an inorganic or organic acid with an ester amine having the formula (I) or (VII), having an average size of 0.1 to 5 µm in the dispersed state, (b) 0.2 to 10 percent by weight of an inorganic electrolyte and the balance of water.
in which R1 and R2 each are a hydrocarbon group having 11 to 23 carbon atoms, straight or branched, saturated or unsaturated, R is a hydrocarbon group having 1 to 24 carbon atoms, straight or branched, saturated or unsaturated, hydroxyethyl, hydroxypropyl, R10 is a hydrocarbon group having 8 to 24 carbon atoms, straight or branched, saturated or unsaturated, and m is 2 or 3. - The composition as claimed in Claim 1, which further comprises (c) a water-insoluble quaternary ammonium salt having one of the formulae (II), (IV), (V) and (VI) at a weight ratio of (a) to (c) in the range between 95/5 and 50/50.
in which R3, R4, R8 and R9 each are an alkyl having 10 to 24 carbon atoms, an alkenyl having 10 to 24 carbon atoms, a beta-hydroxyalkyl having 10 to 24 carbon atoms, R5 and R6 each are an alkyl having 1 to 3 carbon atoms, hydroxyalkyl having 1 to 3 carbon atoms, benzyl or -(C2H4O)q-H, q being 1 to 3, X is a halogen or a monoalkyl sulfate having 1 to 3 carbon atoms in the alkyl. . - The composition as claimed in Claim 1, in which the ester amine (a) has the formula (I).
- The composition as claimed in Claim 1, in which the ester amine (a) has the formula (VII).
- The composition as claimed in Claim 1, in which the inorganic acid for (a) is hydrochloric acid or sulfuric acid and the organic acid is acetic acid, glycolic acid, lactic acid, citric acid, maleic acid, fumaric acid or toluenesulfonic acid.
- The composition as claimed in Claim 1, in which the ester amine for (a) has the formula (I), R1 and R2 each are an alkyl having 15 to 23 carbon atoms or an alkenyl having 15 to 23 carbon atoms and R is an alkyl having 1 to 3 carbon atoms.
- The composition as claimed in Claim 1, in which the ester amine for (a) has the formula (VII) wherein one of R1 and R10 has 16 or more carbon atoms.
- The composition as claimed in Claim 1, in which the inorganic electrolyte is selected from the group consisting of sodium chloride, sodium bromide, calcium chloride and magnesium chloride.
Applications Claiming Priority (6)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP1011690 | 1990-01-19 | ||
| JP10116/90 | 1990-01-19 | ||
| JP143508/90 | 1990-06-01 | ||
| JP14350790A JP2843113B2 (en) | 1990-01-19 | 1990-06-01 | Liquid soft finish |
| JP2143508A JP2851686B2 (en) | 1990-06-01 | 1990-06-01 | Liquid soft finish |
| JP143507/90 | 1990-06-01 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| EP0443313A1 EP0443313A1 (en) | 1991-08-28 |
| EP0443313B1 true EP0443313B1 (en) | 1994-03-23 |
Family
ID=27278842
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP19910100210 Expired - Lifetime EP0443313B1 (en) | 1990-01-19 | 1991-01-08 | Liquid softener composition for fabric |
Country Status (5)
| Country | Link |
|---|---|
| EP (1) | EP0443313B1 (en) |
| DE (1) | DE69101456T2 (en) |
| ES (1) | ES2062574T3 (en) |
| HK (1) | HK152595A (en) |
| MY (1) | MY129954A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| RU2226576C1 (en) * | 2002-08-07 | 2004-04-10 | Открытое акционерное общество "Хитон" | Aerosol agent for anti-electrostatic treatment of synthetic materials |
Families Citing this family (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5659049A (en) * | 1988-02-18 | 1997-08-19 | Virginia Commonwealth University | Antioxidant, antiphospholipase derivatives of ricinoleic acid |
| EP0510879A3 (en) * | 1991-04-26 | 1993-03-17 | Kao Corporation | Liquid softener |
| US5288417A (en) * | 1992-07-06 | 1994-02-22 | Lever Brothers Company, Division Of Conopco, Inc. | Fabric conditioning compositions and process for making them |
| US5288847A (en) * | 1992-08-21 | 1994-02-22 | Colgate-Palmolive Company | Fabric conditioning composition containing alkanol amine ester and acid |
| US5312522A (en) * | 1993-01-14 | 1994-05-17 | Procter & Gamble Company | Paper products containing a biodegradable chemical softening composition |
| US5403499A (en) * | 1993-04-19 | 1995-04-04 | Lever Brothers Company, Division Of Conopco, Inc. | Concentrated fabric conditioning compositions |
| US5468398A (en) * | 1993-05-20 | 1995-11-21 | Colgate-Palmolive Company | Liquid fabric softening composition |
| US5399272A (en) * | 1993-12-17 | 1995-03-21 | The Procter & Gamble Company | Clear or translucent, concentrated biodgradable quaternary ammonium fabric softener compositions |
| US5552137A (en) * | 1994-08-05 | 1996-09-03 | Witco Corporation | Biodegradable quaternary hair conditioners |
| BR9609820A (en) | 1995-07-11 | 1999-07-06 | Procter & Gamble | Softener compositions of concentrated water-dispersible and stable fabrics |
| BR9610336A (en) * | 1995-08-31 | 2005-08-23 | Colgate Palmolive Co | Fabric softening composition and process for softening fabrics |
| US5859271A (en) | 1996-04-15 | 1999-01-12 | Virginia Commonwealth University | Cytoprotective compounds |
| MX2007014173A (en) | 2005-05-18 | 2008-02-07 | Stepan Co | Low solids, high viscosity fabric softener compositions and process for making the same. |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS4835637B1 (en) * | 1970-12-23 | 1973-10-29 | ||
| DE3876196T2 (en) * | 1987-09-23 | 1993-04-15 | Procter & Gamble | LINEAR ALCOXYLATED ALCOHOLS CONTAINING STABLE, BIODEGRADABLE SOFTEN SOFTENER COMPOSITIONS. |
| JPH0756112B2 (en) * | 1988-02-17 | 1995-06-14 | 花王株式会社 | Concentrated softening agent for clothing |
| GB8805837D0 (en) * | 1988-03-11 | 1988-04-13 | Unilever Plc | Fabric conditioning composition |
-
1991
- 1991-01-08 ES ES91100210T patent/ES2062574T3/en not_active Expired - Lifetime
- 1991-01-08 DE DE1991601456 patent/DE69101456T2/en not_active Expired - Fee Related
- 1991-01-08 EP EP19910100210 patent/EP0443313B1/en not_active Expired - Lifetime
- 1991-01-17 MY MYPI9100077 patent/MY129954A/en unknown
-
1995
- 1995-09-21 HK HK152595A patent/HK152595A/en not_active IP Right Cessation
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| RU2226576C1 (en) * | 2002-08-07 | 2004-04-10 | Открытое акционерное общество "Хитон" | Aerosol agent for anti-electrostatic treatment of synthetic materials |
Also Published As
| Publication number | Publication date |
|---|---|
| DE69101456T2 (en) | 1994-07-14 |
| HK152595A (en) | 1995-09-29 |
| MY129954A (en) | 2007-05-31 |
| ES2062574T3 (en) | 1994-12-16 |
| DE69101456D1 (en) | 1994-04-28 |
| EP0443313A1 (en) | 1991-08-28 |
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