Classifications

• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K8/00—Cosmetics or similar toiletry preparations
  • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
  • A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
  • A61K8/40—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
  • A61K8/41—Amines
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K8/00—Cosmetics or similar toiletry preparations
  • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
  • A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
  • A61K8/40—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
  • A61K8/41—Amines
  • A61K8/416—Quaternary ammonium compounds
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K8/00—Cosmetics or similar toiletry preparations
  • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
  • A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
  • A61K8/49—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds
  • A61K8/4906—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with one nitrogen as the only hetero atom
  • A61K8/4926—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with one nitrogen as the only hetero atom having six membered rings
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
  • A61Q19/00—Preparations for care of the skin
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
  • A61Q5/00—Preparations for care of the hair
  • A61Q5/004—Preparations used to protect coloured hair
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
  • A61Q5/00—Preparations for care of the hair
  • A61Q5/008—Preparations for oily hair
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
  • A61Q5/00—Preparations for care of the hair
  • A61Q5/02—Preparations for cleaning the hair
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
  • A61Q5/00—Preparations for care of the hair
  • A61Q5/06—Preparations for styling the hair, e.g. by temporary shaping or colouring
• • C—CHEMISTRY; METALLURGY
  • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
  • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
  • C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
  • C11D3/16—Organic compounds
  • C11D3/26—Organic compounds containing nitrogen
  • C11D3/28—Heterocyclic compounds containing nitrogen in the ring
• • C—CHEMISTRY; METALLURGY
  • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
  • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
  • C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
  • C11D3/16—Organic compounds
  • C11D3/26—Organic compounds containing nitrogen
  • C11D3/30—Amines; Substituted amines ; Quaternized amines
• • C—CHEMISTRY; METALLURGY
  • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
  • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
  • C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
  • C11D3/16—Organic compounds
  • C11D3/26—Organic compounds containing nitrogen
  • C11D3/33—Amino carboxylic acids
• • 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
  • D06M13/35—Heterocyclic compounds
  • D06M13/352—Heterocyclic compounds having five-membered heterocyclic rings
• • 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
  • D06M13/35—Heterocyclic compounds
  • D06M13/355—Heterocyclic compounds having six-membered heterocyclic rings
• • 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
  • D06M13/388—Amine oxides
• • 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
  • 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
• • 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
  • D06M13/477—Compounds containing quaternary nitrogen atoms derived from heterocyclic compounds having six-membered heterocyclic rings
• • D—TEXTILES; PAPER
  • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
  • D06P—DYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
  • D06P1/00—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed
  • D06P1/44—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using insoluble pigments or auxiliary substances, e.g. binders
  • D06P1/64—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using insoluble pigments or auxiliary substances, e.g. binders using compositions containing low-molecular-weight organic compounds without sulfate or sulfonate groups
  • D06P1/642—Compounds containing nitrogen
• • D—TEXTILES; PAPER
  • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
  • D06P—DYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
  • D06P1/00—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed
  • D06P1/44—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using insoluble pigments or auxiliary substances, e.g. binders
  • D06P1/64—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using insoluble pigments or auxiliary substances, e.g. binders using compositions containing low-molecular-weight organic compounds without sulfate or sulfonate groups
  • D06P1/642—Compounds containing nitrogen
  • D06P1/6426—Heterocyclic compounds
• • D—TEXTILES; PAPER
  • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
  • D06P—DYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
  • D06P1/00—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed
  • D06P1/44—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using insoluble pigments or auxiliary substances, e.g. binders
  • D06P1/64—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using insoluble pigments or auxiliary substances, e.g. binders using compositions containing low-molecular-weight organic compounds without sulfate or sulfonate groups
  • D06P1/642—Compounds containing nitrogen
  • D06P1/6428—Compounds containing aminoxide groups
• • D—TEXTILES; PAPER
  • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
  • D06P—DYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
  • D06P5/00—Other features in dyeing or printing textiles, or dyeing leather, furs, or solid macromolecular substances in any form
  • D06P5/02—After-treatment
  • D06P5/04—After-treatment with organic compounds
  • D06P5/06—After-treatment with organic compounds containing nitrogen
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
  • A61K2800/40—Chemical, physico-chemical or functional or structural properties of particular ingredients
  • A61K2800/52—Stabilizers
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
  • A61Q1/00—Make-up preparations; Body powders; Preparations for removing make-up
  • A61Q1/02—Preparations containing skin colorants, e.g. pigments
  • A61Q1/04—Preparations containing skin colorants, e.g. pigments for lips
  • A61Q1/06—Lipsticks
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
  • A61Q11/00—Preparations for care of the teeth, of the oral cavity or of dentures; Dentifrices, e.g. toothpastes; Mouth rinses

Definitions

• the present invention relates to the use of selected hindered nitroxyl, hydroxylamine and hydroxylamine salt compounds for the protection of body care products, household products, textiles and fabrics against the deleterious effects of light, heat and oxygen.
• the stabilized compositions for example comprise dyes that are stabilized against color change.
• WO 01/07550 teaches the treatment of fabric with hindered amine stabilizers.
• the present invention pertains to a stabilized composition
• a stabilized composition comprising
• Gi and G 2 are independently alkyl of 1 to 4 carbon atoms or are together pentamethylene, Zi and Z 2 are each methyl, or Z ⁇ and Z 2 together form a linking moiety which may additionally be substituted by an ester, ether, hydroxy, oxo, cyanohydrin, amide, amino, carboxy or urethane group,
• X is an inorganic or organic anion, such as phosphate, phosphonate, carbonate, bicarbonate, nitrate, chloride, bromide, bisulfite, sulfite, bisulfate, sulfate, borate, formate, acetate, benzoate, citrate, oxalate, tartrate, acrylate, polyacrylate, fumarate, maleate, itaconate, glycolate, gluconate, malate, mandelate, tiglate, ascorbate, polymethacrylate, a carboxylate of nitrilotriacetic acid, hydroxyethylethylenediaminetriacetic acid, ethylenediaminetetraacetic acid or of diethylenetriaminepentaacetic acid, a diethylenetriaminepentamethylenephosphonate, an alkylsulfonate or an arylsulfonate, and where the total charge of cations h is equal to the total charge of anions j.
• X is chloride, bisulfite, bisulfate, suFate, phosphate, nitrate, ascorbate, acetate, citrate or carboxylate of ethylenediaminetetraacetic acid or of diethylenetriaminepentaacetic acid; for instance X is bisulfate or citrate.
• the hindered nitroxyl, hydroxylamine and hydroxylamine salt compounds of component (b) are for example of formulae A to EE and A* to EE*
• E is oxyl or hydroxyl
• R is hydrogen or methyl, in formula A and A*, n is 1 or 2, when n is 1 ,
• Ri is hydrogen, alkyl of 1 to 18 carbon atoms, alkenyl of 2-18 carbon atoms, propargyl, glycidyl, alkyl of 2 to 50 carbon atoms interrupted by one to twenty oxygen atoms, said alkyl substituted by one to ten hydroxyl groups or both interrupted by said oxygen atoms and substituted by said hydroxyl groups, or Ri is alkyl of 1 to 4 carbon atoms substituted by a carboxy group or by -COOZ where Z is hydrogen, alkyl of 1 to 4 carbon atoms or phenyl, or where Z is said alkyl substituted by - (COO " ) n M n+ where n is 1-3 and M is a metal ion from the 1st, 2nd or 3rd group of the periodic table or is Zn, Cu, Ni or Co, or M is a group N ⁇ + (R 2 ) 4 where R 2 is alkyl of 1 to 8 carbon atoms or benzyl, when n
• R 2 is -CH 2 (OCH 2 CH 2 ) n OCH 3 where n is 1 to 12, or R 2 is cycloalkyl of 5 to 12 carbon atoms, aryl of 6 to 12 carbon atoms, or said aryl substituted by one to four alkyl groups of 1 to 4 carbon atoms, or R 2 is -NHR 3 where R 3 is alkyl of 1 to 18 carbon atoms, cycloalkyl of 5 to 12 carbon atoms, aryl of 6 to 12 carbon atoms, or said aryl substituted by one to four alkyl of 1 to 4 carbon atoms, or R 2 is -N(R 3 ) 2 where R 3 is as defined above, when m is 2, R 2 is alkylene of 1 to 12 carbon atoms, alkenylene of 4 to 12 carbon atoms, xylylene, alkylene of 2 to 12 carbon atoms interrupted by -COO-, or R> is -CH 2 (OCH 2 CH 2 ) n
• R 2 is alkanetriyl of 3 to 8 carbon atoms or benzenetriyl, or when m is 4,
• R 2 is alkanetetrayl of 5 to 8 carbon atoms or benzenetetrayl, in formula C and C*, R-io is hydrogen, alkyl of 1 to 18 carbon atoms, cycloalkyl of 5 to 12 carbon atoms, aralkyl of 7 to 15 carbon atoms, alkanoyl of 2 to 18 carbon atoms, alkenoyl of 3 to 5 carbon atoms or benzoyl, x is 1 or 2, when x is 1 ,
• R 11 is hydrogen, alkyl of 1 to 18 carbon atoms, alkenyl of 2 to 18 carbon atoms, propargyl, glycidyl, alkyl of 2 to 50 carbon atoms interrupted by one to twenty oxygen atoms, said alkyl substituted by one to ten hydroxyl groups or both interrupted by said oxygen atoms and substituted by said hydroxyl groups, or
• Rn is alkyl of 1 to 4 carbon atoms substituted by a carboxy group or by -COOZ where Z is hydrogen, alkyl of 1 to 4 carbon atoms or phenyl, or where Z is said alkyl substituted by - (COO " ) n M n+ where n is 1-3 and M is a metal ion from the 1st, 2nd or 3rd group of the periodic table or is Zn, Cu, Ni or Co, or M is a group N ⁇ + (R 2 ) 4 where R 2 is hydrogen, alkyl of 1 to 8 carbon atoms or benzyl, or when x is 2,
• Rn is alkylene of 1 to 12 carbon atoms, alkenylene of 4 to 12 carbon atoms, xylylene or alkylene of 1 to 50 carbon atoms interrupted by one to twenty oxygen atoms, substituted by one to ten hydroxyl groups or both interrupted by said oxygen atoms and substituted by said hydroxyl groups, in formula D and D*,
• R 10 is as defined above, y is 1 to 4, and
• R 12 is defined as R 2 above in formula E and E*, k is 1 or 2, when k is 1 ,
• R 20 and R 21 are independently alkyl of 1 to 12 carbon atoms, alkenyl of 2 to 12 carbon atoms or aralkyl of 7 to 15 carbon atoms, or R> 0 is also hydrogen, or
• R 20 and R 21 together are alkylene of 2 to 8 carbon atoms or said alkylene substituted by hydroxyl, or are acyloxy-alkylene of 4 to 22 carbon atoms, or when k is 2,
• R 20 and R 21 are together (-CH 2 ) 2 C(CH 2 -) 2 , in formula F and F*, R 30 is hydrogen, alkyl of 1 to 18 carbon atoms, benzyl, glycidyl, or alkoxyalkylof 2 to 6 carbon atoms, g is 1 or 2, when g is 1 , R 31 is defined as R-i above when n is 1 , when g is 2, R 31 is defined as R ⁇ above when n is 2, in formula G and G*, Qi is -NR 41 - or -O-, E t is alkylene of 1 to 3 carbon atoms, or E, is -CH 2 -CH(R 42 )-O- where R 2 is hydrogen, methyl or phenyl, or Ei is -(CH 2 ) -NH- or E ⁇ is a direct bond, R 0 is hydrogen or alkyl of 1 to 18 carbon atoms, R 1 is hydrogen, alkyl of 1 to 18 carbon atoms, cycl
• R 41 is -CH 2 -CH(R 2 )-OH
• R 42 is as defined above, in formula H and H*, p is 1 or 2,
• T 4 is as defined for Rn when x is 1 or 2, M and Y are independently methylene or carbonyl, for instance M is methylene and Y is carbonyl, in formula I and I*, this formula denotes a recurring structural unit of a polymer where T is ethylene or 1 ,2- propylene or is the repeating structural unit derived from an alpha-olefin copolymer with an alkyl acrylate or methacrylate, and where q is 2 to 100,
• Qi is -N(R 41 )- or -O- where R 41 is as defined above, in formula J and J*, r is 1 or 2,
• T 7 is as defined for R-, when n is 1 or 2 in formula A, for example T 7 is octamethylene when r is 2, in formula L and L*, u is 1 or 2, Ti 3 is as defined for R, when n is 1 or 2 in formula A, with the proviso that T 13 is not hydrogen when u is 1 , in formula M and M * , E-, and E 2 , being different, each are -CO- or -N(E 5 )- where E 5 is hydrogen, alkyl of 1 to 12 carbon atoms or alkoxycarbonylalkyl of 4 to 22 carbon atoms, for instance Ei is -CO- and E 2 is -N(E 5 )-, E 3 is hydrogen, alkyl of 1 to 30 carbon atoms, phenyl, naphthyl, said phenyl or said naphthyl substituted by chlorine or by alkyl of 1 to 4 carbon atoms, or phe ⁇ ylalkyl of 7 to
• E 4 is hydrogen, alkyl of 1 to 30 carbon atoms, phenyl, naphthyl or phenylalkyl of 7 to 12 carbon atoms, or E 3 and E 4 together are polymethylene of 4 to 17 carbon atoms, or said polymethylene substituted by one to four alkyl of 1 to 4 carbon atoms, for example methyl, in formula N,
• Ri is as defined for R ⁇ in formula A when n is 1
• G 3 is a direct bond, alkylene of 1 to 12 carbon atoms, phenylene or -NH-G NH- where G ⁇ s alkylene of 1 to 12 carbon atoms, in formula O and O*
• R 10 is as defined for R 10 in formula C, in formula P and P*
• E 6 is an aliphtic or aromatic tetravalent radical, for example neopentanetetrayl or benzenetetrayl, in formula T and T*
• R 51 is hydrogen, alkyl of 1 to 18 carbon atoms, cycloalkyl of 5 to 12 carbon atoms, or aryl of
• R 52 is hydrogen or alkyl of 1 to 18 carbon atoms, or R 51 and R 52 together of alkylene of 4 to 8 carbon atoms, f is 1 or 2, when f is 1 , R 50 is as defined for R in formula C when x is 1 , or R 50 is -(CH 2 ) z COOR 54 where z is 1 to 4 and R 54 is hydrogen or alkyl of 1 to 18 carbon atoms, or R 54 is a metal ion from the 1st,
• R50 is as defined for R in formula C when x is 2
• R5 3 , R ⁇ , R55 and R 56 are independently alkyl of 1 to 4 carbon atoms or are together pentamethylene.
• R58, R59 and R 60 are independently alkyl of 1 to 4 carbon atoms or are together pentamethylene.
• W and W* are independently alkyl of 1 to 4 carbon atoms or are together pentamethylene.
• R ⁇ ii R ⁇ 2> ⁇ 3 and R 6 are independently alkyl of 1 to 4 carbon atoms or are together pentamethylene,
• R 65 is alkyl of 1 to 5 carbon atoms
• M is hydrogen or oxygen, wherein in formulas X to CC and X* to CC* n is 2 to 3,
• G is hydrogen, methyl, ethyl, butyl or benzyl, m is 1 to 4, x is 1 to 4, when x is 1 ,
• Ri and R 2 are independently alkyl of 1 to 18 carbon atoms, said alkyl interrupted by one to five oxygen atoms, said alkyl substituted by 1 to 5 hydroxyl groups or said alkyl both interrupted by said oxygen atoms and substituted by said hydroxyl groups; cycloalkyl of 5 to 12 carbon atoms, aralkyl of 7 to 15 carbon atoms, aryl of 6 to 10 carbon atoms or said aryl substituted by one to three alkyl of 1 to 8 carbon atoms, or Riis also hydrogen, or Ri and R 2 are together tetramethylene, pentamethylene, hexamethylene or 3- oxapentamethylene, when x is 2,
• R-i is hydrogen, alkyl of 1 to 8 carbon atoms, said alkyl interrupted by one or two oxygen atoms, said alkyl substituted by a hydroxyl group, or said alkyl both interrupted by one or two oxygen atoms and substituted by a hydroxyl group,
• R 2 is alkylene of 2 to 18 carbon atoms, said alkylene interrupted by one to five oxygen atoms, said alkylene substituted by 1 to 5 hydroxyl groups or said alkylene both interrupted by said oxygen atoms and substituted by said hydroxyl groups; o-, m- or p- phenylene or said phenylene substituted by one or two alkyl of 1 to 4 carbon atoms, or
• R 2 is -(CH 2 ) k O[(CH 2 ) k O] h (CH 2 ) k - where k is 2 to 4 and h is 1 to 40, or
• R., and R 2 together with the two N atoms to which they are attached are piperazin-1 ,4-diyl, when x is 3,
• R. is hydrogen
• R 2 is alkylene of 4 to 8 carbon atoms interrupted by one nitrogen atom, when x is 4,
• R 2 is alkylene of 6 to 12 carbon atoms interrupted by two nitrogen atoms
• R 3 is hydrogen, alkyl of 1 to 8 carbon atoms, said alkyl interrupted by one or two oxygen atoms, said alkyl substituted by a hydroxyl group, or both interrupted by one or two oxygen atoms and substituted by a hydroxyl group,
• Q is an alkali metal salt, ammonium or N + (G 1 ) 4 in formula DD and DD* m is 2 or 3, when m is 2,
• G is -(CH 2 CHR-O) r CH 2 CHR-, where r is 0 to 3, and R is hydrogen or methyl, and when m is 3,
• G is glyceryl, in formula EE and EE*
• G 2 is -CN, -CONH 2 or -COOG 3 where G 3 is hydrogen, alkyl of 1 to 18 carbon atoms or phenyl,
• X is an inorganic or organic anion, such as phosphate, phosphonate, carbonate, bicarbonate, nitrate, chloride, bromide, bisulfite, sulfite, bisulfate, sulfate, borate, formate, acetate, benzoate, citrate, oxalate, tartrate, acrylate, polyacrylate, fumarate, maleate, ita- conate, glycolate, gluconate, malate, mandelate, tiglate, ascorbate, polymethacrylate, a carboxylate of nitrilotriacetic acid, hydroxyethylethylenediaminetriacetic acid, ethylenediaminetetraacetic acid or of diethylenetriaminepentaacetic acid, a diethylenetriamine- pentamethylenephosphonate, an alkylsulfonate or an arylsulfonate, and where the total charge of cations h is equal to the total charge of anions j
• the compounds of component (b) are those of formulas A, A*, B, B*, C, C*, D,
• R is hydrogen, in formula A and A* n is 1 or 2, when n is 1 ,
• Ri is hydrogen, alkyl of 1 to 6 carbon atoms, alkenyl of 2-6 carbon atoms, propargyl, glycidyl, alkyl of 2 to 20 carbon atoms interrupted by one to ten oxygen atoms, said alkyl substituted by one to five hydroxyl groups or both interrupted by said oxygen atoms and substituted by said hydroxyl groups, or Ri is alkyl of 1 to 4 carbon atoms substituted by a carboxy group or by -COOZ where Z is hydrogen or alkyl of 1 to 4 carbon atoms, when n is 2, Ri is alkylene of 1 to 8 carbon atoms, alkenylene of 4 to 8 carbon atoms, alkylene of 1 to 20 carbon atoms interrupted by one to ten oxygen atoms, substituted by one to five hydroxyl groups or both interrupted by said oxygen atoms and substituted by said hydroxyl groups, in formula B and B* m is 1 or 2 when m is 1 ,
• R 2 is alkyl of 1 to 4 carbon atoms or R> is CH 2 (OCH 2 CH 2 ) n OCH 3 where n is 1 to 12, or R 2 is phenyl, or said phenyl substituted by one to three methyl groups, R 2 is -NHR 3 where R 3 is alkyl of 1 to 4 carbon atoms or phenyl, or said phenyl substituted by one or two methyl groups, when m is 2, R 2 is alkylene of 1 to 8 carbon atoms, alkenylene of 4 to 8 carbon atoms, or R 2 is
• R 2 is NHR 4 NH where R-i is of 2 to 6 carbon atoms, aralkylene of 8 to 15 carbon atoms or arylene of 6 to 12 carbon atoms, R 2 is -CO- or -NHCONH, in formula C and C*,
• R 10 is hydrogen or, alkanoyl of 1 to 3 carbon atoms, x is 1 or 2, when x is 1 ,
• R 11 is hydrogen, alkyl of 1 to 6 carbon atoms or glycidyl
• Rn is alkyl of 1 to 4 carbon atoms substituted by a carboxy group or by COOZ where Z is hydrogen or alkyl of 1 to 4 carbon atoms, when x is 2,
• Rn is alkylene of 1 to 6 carbon atoms, in formula D and D*, R-io is hydrogen, y is 1 or 2, R12 is defined as R 2 above, in formula Y, Y*, Z and Z*, x is 1 or 2, when x is 1 ,
• Ri and R 2 are independently alkyl of 1 to 4 carbon atoms, or Ri and R 2 are together tetramethylene, or pentamethylene,
• R 2 is hydrogen or alkyl of 1 to 4 carbon atoms, said alkyl group substituted by a hydroxyl group, when x is 2,
• Ri is hydrogen, alkyl of 1 to 4 carbon atoms, said alkyl substituted by a hydroxyl group, R is alkylene of 2 to 6 carbon atoms, R 3 is as defined above.
• the compounds of component (b) are those of formulas A, A*, B,B*, C, C*, D,
• R is hydrogen, in formula A and A*, h is 1,
• Ri is hydrogen, alkyl of 1 to 4 carbon atoms, glycidyl, alkyl of 2 to 4 carbon atoms interrupted by one or two oxygen atoms, said alkyl substituted by one or two hydroxyl groups or both interrupted by said oxygen atoms and substituted by said hydroxyl groups, or Ri is alkyl of 1 to 4 carbon atoms substituted by -COOZ where Z is hydrogen or alkyl of 1 to
• R 2 is alkyl of 1 to 4 carbon atoms or R, is CH 2 (OCH 2 CH 2 ) n OCH 3 where n is 1 to 4, when m is 2,
• R 2 is alkylene of 1 to 8 carbon atoms, in formula C and C*,
• Rio is hydrogen or alkanoyl of 1 or 2 carbon atoms
• x is 1 or 2
• R11 is hydrogen, alkyl of 1 to 4 carbon atoms or glycidyl
• R1 1 is alkyl of 1 to 4 carbon atoms substituted by COOZ where Z is hydrogen or alkyl of 1 to
• R 11 is alkylene of 1 to 6 carbon atoms, in formula D and D*, Rio is hydrogen, y is 1 or 2, R 12 is defined as R 2 above.
• the hindered nitroxyl, hydroxylamine and hydroxylamine salt compounds of component (b) are selected from bis(1-oxyl-2,2-6-6-tetramethylpiperidin-4-yl) sebacate; bis(1 -hydroxy-2,2-6-6-tetramethylpiperidin-4-yl) sebacate; 1 -hydroxy-2,2-6-6-tetramethyl-4- acetoxypiperidinium citrate; 1-oxyl-2,2,6,6-tetramethyl-4-acetamidopiperidine; 1-hydroxy- 2,2,6,6-tetramethyl-4-acetamidopiperidine; 1-hydroxy-2,2,6,6-tetramethyl4-acetamidopi- peridinium bisulfate; 1-oxyl-2,2,6,6-tetramethyl-4-oxo-piperidine; 1-hydroxy -2,2,6,6-tetra- methyl-4-oxo-piperidine; 1-hydroxy -2,2,6,6-tetramethyl-4-oxo-pipe
• the hindered nitroxyl, hydroxylamine and hydroxylamine salt compounds of component (b) are selected from 1-oxyl-2,2,6,6-tetramethyl-4-hydroxypiperidine; 1-hydroxy- 2,2,6,6-tetramethyl-4-hydroxypiperidine; 1-hydroxy-2,2,6,6-tetramethyl-4-hydrox ⁇ iperidinium chloride; 1-hydroxy-2,2,6,6-tetramethyl-4-hydroxypiperidinium acetate; 1-hydroxy-2,2,6,6- tetramethyl-4-hydroxypiperidinium bisulfate; 1 -hydroxy-2,2,6,6-tetramethyl4-hydroxypiperi- dinium citrate; bis(1-hydroxy-2,2,6,6-tetramethyl-4-hydroxypperidinium) citrate; tris(1- hydroxy-2,2,6,6-tetramethyl-4-hydroxypiperidinium) citrate; tetra(1-hydroxy-2,2,6,6- tetramethyl-4-hydroxypiperidinium) ethylenedi
• the compounds of component (b) are selected from 1-hydroxy-2,2,6,6-tetra- methyl-4-hydroxypiperidinium citrate; bis(1 -hydroxy-2,2,6,6-tetramethyl-4-hydrox iperi- dinium) citrate; tris(1-hydroxy-2,2,6,6-tetramethyl4-hydroxypiperidinium) citrate; 1-hydroxy- 2,2,6,6-tetramethyl-4-hydroxypiperidinium DTPA; bis(1 -hydroxy-2,2,6,6-tetramethyl-4-hydro- xypiperidinium) DTPA; tris(1-hydroxy-2,2,6,6-tetramethyl-4-hydroxypiperidinium) DTPA; tetrakis(1-hydroxy-2,2,6,6-tetramethyl-4-hydroxypiperidinium) DTPA; pentakis(1-hydroxy- 2,2,6,6-tetramethyl-4-hydroxypiperidinium) DTPA; 1 -hydroxy-2,2,6,6-tetramethyl-4-
• EDTA ethylenediaminetetraacetic acid
• DTPA diethylenetriaminepentaacetic acid
• HEDTA hydroxyethylethylenediaminetriacetic acid
• NTA ni- trilotriacetic acid
• DTPMPA diethylenetriaminepentamethylenephosphonic acid
• compositions may comprise further traditional additives, for example ultraviolet (UV) light absorbers and antioxidants.
• UV ultraviolet
• the present invention further pertains to a stabilized composition
• a stabilized composition comprising (a) a body care product, household product, textile or fabric, (b) an effective stabilizing amount of at least one compound selected from the group consisting of
• the UV absorbers are for example selected from group consisting of the 2H-benzotriazoles, the s-triazines, the benzophenones, the ⁇ -cyanoacrylates, the oxanilides, the benzocazino- nes, the benzoates and the ⁇ -alkyl cinnamates.
• the UV absorbers are for example 2,4,6-tris(2-hydroxy-4-octyloxyphenyl)-1,3,5-triazine; 2-(2,4-dihydroxyphenyl)-4,6-bis(2,4-dimethylphenyl)-1 ,3,5-triazine; 2,4-bis(2-hydroxy-4- propyloxyphenyl)-6-(2,4-dimethylphenyl)-1 ,3,5-triazine; 2-(2-hydroxy-4-octyloxyphenyl)-4,6- bis(4-methylphenyl)-1 ,3,5-triazine; 2-(2-hydroxy-4-dodecyloxyphenyl)-4,6-bis(2,4-dimethyl- phenyl)-1 ,3,5-triazine; 2-[2-hydroxy-4-(2-hydroxy-3-butyloxypropyloxy)phenyl]-4,6-bis(2,4- dimethylphenyl)-1 ,3,5-triazine;
• suitable UV absorbers are selected from 3-(2H-benzotriazol-2-yl)-4-hydroxy-5- (l-methylpropyl)-benzenesulfonic acid monosodium salt; 3-tert-butyl-4-hydroxy-5-(2H-benzo- triazol-2-yl)-hydrocinnamic acid and sodium salt; 2-(2-hydroxy-3,5-di-tert-butylphenyl)-2H- benzotriazole; 2-(2-hydroxy-3, 5-di-tert-amylphenyl)-2H-benzotriazole; 4, 6-bis(2,4-dimethyl- phenyl)-2-(4-(3-dodecyloxy*-2-hydroxypropoxy)-2-hydroxyphenyl)-s-triazine (*is mixture of C ⁇ 2 . ⁇ 4 oxy isomers); 12-hydroxy-3,6,9-trioxadodecyl 3-tert-butyl-4-hydroxy-5-(2H-(2
• antioxidants are for example selected from the hindered phenolic and benzofuranone stabilizers.
• Suitable antioxidants are for example selected from the group consisting of
• M H, ammonium, alkali
• the hindered amine light stabilizers (HALS) of component (c) are for example known commercial compounds. They are for example selected from the group consisting of bis(2,2,6,6-tetramethylpiperidin-4-yl)sebacate, bis(2,2,6,6-tetramethylpiperidin-4-yl)succinate, bis(1,2,2,6,6-pentamethylpiperidin-4-yl)sebacate, n-butyl-3,5-di-tert-butyl-4-hydroxybenzyl- malonic acid-bis(1,2, 2,6,6-pentamethylpiperidyl)ester, the condensate of 1-hydroxyethyl- 2,2,6,6-tetramethyl-4-hydroxypiperidine and succinic acid, the condensate of N,N'- bis(2,2,6,6-tetramethyl4-piperidyl)hexamethylenediamine and 4-tert-octylamino-2,6-dichloro- 1 ,3,
• n is a value from 5-50
• R H or CH
• the complex formers of component (c) are for example nitrogen-containing complex formers or polyanionically-derived natural polysaccharides, for example those containing phosphate, phosphonate or methylphosphonate groups, such as chitin derivatives, e.g. sulfochitin, carboxymethylchitin, phosphochitin or chitosan derivatives, for example sulfochitosan, carboxymethylchitosan or phosphochitosan.
• chitin derivatives e.g. sulfochitin, carboxymethylchitin, phosphochitin or chitosan derivatives, for example sulfochitosan, carboxymethylchitosan or phosphochitosan.
• the complex formers are for example selected from the group consisting of ethylenadiamine- tetracetic acid (EDTA), nitrilotriacetic acid (NTA), D-alaninediacetic acid (EDETA) or
• the present stabilizer systems are particularly suitable for stabilizing body care products, in particular for use in skin-care products, as bath and shower products, preparations containing fragrances and odoriferous substances, hair-care products, dentifrices, deodorizing and antiperspirant preparations, decorative preparations, light protection formulations and preparations containing active ingredients.
• Suitable skin-care products are, in particular, body oils, body lotions, body gels, treatment creams, skin protection ointments, shaving preparations, such as shaving foams or gels, skin powders, such as baby powder, moisturising gels, moisturising sprays, revitalising body sprays, cellulite gels and peeling preparations.
• fragrances and odoriferous substances are in particular scents, perfumes, toilet waters and shaving lotions (aftershave preparations).
• Suitable hair-care products are, for example, shampoos for humans and animals, in particular dogs, hair conditioners, products for styling and treating hair, perming agents, hair sprays and lacquers, hair gels, hair fixatives and hair dyeing or bleaching agents.
• Suitable dentifrices are in particular tooth creams, toothpastes, mouth-washes, mouth rinses, anti-plaque preparations and cleaning agents for dentures.
• Suitable decorative preparations are in particular lipsticks, nail varnishes, eye shadows, mascaras, dry and moist make-up, rouge, powders, depilatory agents and suntan lotions.
• Suitable cosmetic formulations containing active ingredients are in particular hormone preparations, vitamin preparations, vegetable extract preparations and antibacterial preparations.
• the present body care products can be in the form of creams, ointments, pastes, foams, gels, lotions, powders, make-ups, sprays, sticks or aerosols.
• the present stabilizer systems may be present in the oil phase or in the aqueous or aqueous/alcoholic phase.
• the additives of component (b) are present, for example, in the body care and household products in a concentration of about 5 to about 10000 ppm, based on the total formulation, for example from about 10 to about 5000 ppm, for example from about 100 to about 1000 ppm.
• the additives of component (b) are present in the body care and household products in a concentration of about 5, 10, 15, 20, 25, 35, 40, 45 or 50 ppm, based on the total formulation.
• the additives of component (b) are present from about 5 to about 1000 ppm in the formulations (compositions) of this invention.
• Laundry detergents, fabric softeners or other products, from which the additives of component (b) are intended for deposition onto fabrics with use, are considered household products of this invention, and the above concentration levels also pertain thereto.
• the present additives of component (b) are effective at stabilizing the laundry detergents and fabric softeners, as well as the fabrics treated therewith.
• Creams are oil-in-water emulsions containing more than 50% water.
• the oil-containing base used therein is usually mainly fatty alcohols, for example lauryl, cetyi or stearyl alcohol, fatty acids, for example palmitic or stearic acid, liquid to solid waxes, for example isopropyl- myristate or beeswax and/or hydrocarbon compounds, such as paraffin oil.
• fatty alcohols for example lauryl, cetyi or stearyl alcohol
• fatty acids for example palmitic or stearic acid
• liquid to solid waxes for example isopropyl- myristate or beeswax
• hydrocarbon compounds such as paraffin oil.
• Suitable emulsifiers are surfactants having primarily hydrophilic properties, such as the corresponding non- ionic emulsifiers, for example fatty acid esters of polyalcohols of ethylene oxide adducts, such as polyglycerol fatty acid ester or polyoxyethylenesorbitan fatty add ether (Tween trademarks); polyoxyethylene fatty alcohol ether or their esters or the corresponding ionic emulsifiers, such as the alkali metal salts of fatty alcohol sulfonates, sodiim cetyl sulfate or sodium stearyl sulfate, which are usually used together with fatty alcohols, such as cetyl alcohol or stearyl alcohol.
• creams contain agents which reduce water loss during evaporation, for example polyalcohols, such as glycerol, sorbitol, propylene glycol, and/or polyethylene glycols.
• Ointments are water-in-oil emulsions which contain up to 70%, for instance not more than 20 to 50%, of water or of an aqueous phase.
• the oil-containing phase contains predominantly hydrocarbons, such as paraffin oil and/or solid paraffin which for instance contains hydroxy compounds, for example fatty alcohol or their esters, such as cetyl alcohol or wool wax for improving the water absorption.
• Emulsifiers are corresponding lipophilic substances, such as sorbitan fatty acid ester.
• the ointments contain moisturisers such as polyalcohols, for example glycerol, propylene glycol, sorbitol and/or polyethylene glycol as well as preservatives.
• Rich creams are anhydrous formulations and are produced on the basis of hydrocarbon compounds, such as paraffin, natural or partially synthetic fats, for example coconut fatty add triglycerides or, for instance, hardened oils and glycerol partial fatty acid esters.
• hydrocarbon compounds such as paraffin, natural or partially synthetic fats, for example coconut fatty add triglycerides or, for instance, hardened oils and glycerol partial fatty acid esters.
• Pastes are creams and ointments containing powdered ingredients which absorb secretions, for example metal oxides, such as titanium dioxide or zinc oxide, and also tallow and/or aluminium silicates which bind the moisture or the absorbed secretion.
• metal oxides such as titanium dioxide or zinc oxide
• aluminium silicates which bind the moisture or the absorbed secretion.
• Foams are liquid oil-in-water emulsions in aerosol form.
• Hydrocarbon compounds are used, inter alia, for the oil-containing phase, for example paraffin oil, fatty alcohols, such as cetyl alcohol, fatty acid esters, such as isopropylmyristate and/or waxes.
• Suitable emulsifiers are, inter alia, mixtures of emulsifiers having predominantly hydrophilic properties, for example polyoxyethylenesorbitan fatty acid ester, and also emulsifiers having predominantly lipophilic properties, for example sorbitan fatty acid ester.
• Commercially available additives are usually additionally employed, for example preservatives.
• Gels are, in particular, aqueous solutions or suspensions of active substances in which gel formers are dispersed or swelled, in particular cellulose ethers, such as methyl cellulose, hydroxyethyl cellulose, carboxymethyl cellulose or vegetable hydrocolloids, for example sodium alginate, tragacanth or gum Arabic and polyacrylate thickener systems.
• the gels for example additionally contain polyalcohols, such as propylene glycol or glycerol as moisturisers and wetting agents, such as polyoxyethylenesobitan fatty acid ester.
• the gels furthermore contain commercially available preservatives, such as benzyl alcohol, phenethyl alcohol, phenoxyethanol and the like.
• present body care products, household products, textiles and fabrics have high stability towards color changes and chemical degradation of the ingredients present in these products.
• present compositions that comprise a dye are found to have excellent color stability.
• the present invention further pertains to a stabilized composition
• a stabilized composition comprising (a) a body care product, household product, textile or fabric, (b) an effective stabilizing amount of at least one compound selected from the group consisting of
• Dyes according to the present invention are for example:
• iron oxide Iron Oxide Red, Iron Oxide Yellow, Iron Oxide Black, etc.
• Ultramarines Chromium Oxide Green or Carbon Black
• anionic or cationic dyes like acid dyes (anionic), basic dyes (cationic), direct dyes, reactive dyes or solvent dyes.
• chromophores Azo- (mono-, di, tris-, or poly-)stilbene-, carotenoide-, diarylmethan-, triarylmethan-, xanthen-, acridin-, quinoline, methin- (also polymethin-), thiazol-, indamin-, indophenol-, azin-, oxazin, thiazin-, anthraquinone-, indigoid-, phtalocyanine- and further synthetic, natural and/or inorganic chromophores.
• the present stabilizer systems are also used in household cleaning and treatment agents, for example in laundry products and fabric softeners, liquid cleansing and scouring agents, glass detergents, neutral cleaners (all-purpose cleaners), acid household cleaners (bath), bathroom cleaners, for instance in washing, rinsing and dishwashing agents, kitchen and oven cleaners, clear rinsing agents, dishwasher detergents, shoe polishes, polishing waxes, floor detergents and polishes, metal, glass and ceramic cleaners, textile-care products, rug clea- ners and carpet shampoos, agents for removing rust, color and stains (stain remover salt), furniture and multipurpose polishes and leather and vinyl dressing agents (leather and vinyl sprays) and air fresheners.
• household cleaning and treatment agents for example in laundry products and fabric softeners, liquid cleansing and scouring agents, glass detergents, neutral cleaners (all-purpose cleaners), acid household cleaners (bath), bathroom cleaners, for instance in washing, rinsing and dishwashing agents, kitchen
• the present invention also concerns home care and fabric care products such as drain cleaners, disinfectant solutions, upholstery cleaners, automotive care products (e.g., to clean and/or polish and protect paint, tires, chrome, vinyl, leather, fabric, rubber, plastic and fabric), degreasers, polishes (glass, wood, leather, plastic, marble, granite, and tile, etc.), and metal polishes and cleaners.
• Antioxidants are suitable to protect fragrances in above products as well as in dryer sheets.
• the present invention also relates to home care products such as candles, gel candles, air fresheners and fragrance oils (for the home).
• the stabilizers of the present invention may be employed in fabric treatment that takes place after use of the fabric, referred to as fabric care. Such treatments include laundering, which uses detergents and/or fabric conditioner, and the application of non-detergent based fabric care products, such as spray-on products. When employed in this fashion, the present stabilizers are intended for deposition onto the fabric and used to protect the fabric, colorants and fragrances associated with said these fabrics from environmental damage.
• Typical examples of household cleaning and treating agents are:
• the present stabilizers are for example incorporated by dissolution in an oil phase or alcoholic or water phase, where required at elevated temperature.
• the present invention also pertains to a method of stabilizing a body care product, household product, textile or fabric, which comprises incorporating therein or applying thereto at least one compound of the formulae (I), (II) and (III), for example at least one compound of the formulae A to EE and A* to EE*.
• the present stabilizers are applied thereto via deposition from for instance detergents, fabric conditioners or non-detergent based fabric care products.
• the present fabrics are natural or synthetic, and may be woven or nonwoven.
• the present invention also pertains to a method of stabilizing a body care product, household product, textile or fabric, each of which contain a dye, which comprises incorporating therein or applying thereto at least one compound of the formulae (I), (II) and (III), for example at least one compound of the formulae A to EE and A* to EE*.
• the stabilizers of formulae (I), (II) and (111) are very effective towards the stabilization of dyes in the present compositions.
• the textiles of this invention are for example textile fiber materials, for example nitrogen- containing or hydroxy-group-containing fiber materials, for instance textile fiber materials selected from cellulose, silk, wool, synthetic polyamides, leather and polyurethanes. Included are cotten, linen and hemp, pulp and regenerated cellulose Included also are cellulosic blends, for example mixtures of cotton and polyamide or cotton/polyester blends.
• the additives of the present invention are for example applied to textiles in a dyeing or printing process, or in a finishing process.
• the additives may be appliedas part of a dye formulation.
• the additives may be applied to textiles for example h an ink-jet printing process.
• the additives are for example applied as part of an aqueous dye solution or printing paste. They may be applied in an exhaust method or dyeing by the padder dyeing method, in which the textiles are impregnated with aqueous dye solutions, which may contain salts, and the dyes and additives are fixed, after an alkali treatment or in the presence of alkali, if appropriate with the action of heat or by storage at room temperature for several hours. After fixing, the dyeings or prints are rinsed thoroughly with cold and hot water, if appropriate with the addition of an agent which has a dispersing action and promotes diffusion of the non-fixed portions.
• the dye or ink formulations for application to textiles may comprise further customary additves, for example surfactants, antifoams, antimicrobials and the like, for example as disclosed in U.S. Pat. Nos. 6,281,339, 6,353,094 and 6,323,327, the disclosures of which are hereby incorporated by reference.
• Aqueous based test formulations are prepared as follows:
• sodium laureth sulfate (30%, TEXAPON NSO, Cognis) 30% cocamidopropylbetaine (30%, DEHYTON K, Cognis) 10% colorant 0.001% stabilizer 0.05% citric acid (10% aqueous solution) to pH 6 deionized water to 100%
• the bottles are also exposed to accelerated fluorescent lighting, Philips, 40 Watt, Daylight Deluxe (D65), full exposure to light.
• Example 1 Aqueous model formulation with PURICOLOR BLUE ABL9 Aqueous formulations are prepared where the colorant is PURICOLOR BLUE ABL9 (FD&C Blue No. 1). Exposure is in a WeatherOmeter. Delta E is measured at 20-hour intervals. Results are below:
• the stabilizers of the present invention provide far greater color stability than state of the art stabilizers (A) and (B).
• Example 2 Aqueous model formulation with PURICOLOR RED ARE33 (D&C Red No. 33) Aqueous formulations are prepared where the colorant is PURICOLOR RED ARE33. Exposure is in a WeatherOmeter. Delta E is measured at 20 hour intervals. Results are below: delta E stabilizer 20 hrs. 40 hrs. 60 80 hrs. none (control) 55 — —
• the stabilizers of the present invention provide far greater color stability than state of the art stabilizers (A) and (B).
• Example 3 Aqueous model formulation with FD&C Red No. 40
• Aqueous formulations are prepared where the colorant is FD&C Red No. 40. Exposure is in a
• the stabilizers of the present invention provide far greater color stability than state of the art stabilizers (A) and (B).
• Example 4 Aqueous model formulation with PURICOLOR BLUE ABL9
• Aqueous formulations are prepared where the colorant is PURICOLOR BLUE ABL9.
• the stabilizers of the present invention provide far greater color stability than state of the art stabilizers (A) and (B).
• Example 5 Aqueous model formulation with D&C Red No. 33
• Aqueous formulations are prepared where the colorant is PURICOLOR RED ARE33 (D&C Red No. 33). Exposure is to fluorescent light. Delta E is measured at weekly intervals. Results are below:
• the stabilizers of the present invention provide far greater color stability than state of the art stabilizers (A) and (B).
• Example 6 Aqueous model formulation with FD&C Red No. 40
• Aqueous formulations are prepared where the colorant is FD&C Red No. 40. Exposure is to fluorescent light. Delta E is measured at weekly intervals. Results are below:
• the stabilizers of the present invention provide far greater color stability than state of the art stabilizers (A) and (B).
• phase A The components of phase A are thoroughly mixed in a homogenizer for 10 min at 75-80°C.
• the water phase B likewise heated to 75-80°C beforehand, is slowly added and the mbture is homogenized for 1 min.
• the mixture is cooled, with stirring, to 40°C and then phases C and E are added and the mixture is homogenized for 1 min.
• phase D is added and the mixture is homogenized for 1/2 min and cooled, with stirring, to room temperature. Excellent results are achieved.
• Example 8 Preparation of a toilet water (w/w) %
• the components are thoroughly mixed in the cited sequence at 50°C, a clear homogeneous solution being obtained.
• the UV absorber is one of the present disclosure, for example 3- (2H-benzotriazol-2-yl)-4-hydroxy-5-(1-methylpropyl)-benzenesulfonic acid monosodium salt. Excellent results are achieved.
• hydroxypropyl cellulose is first predissolved in half of the alcohol (Vortex mixer) and is charged with the aminomethylpropanol.
• the other components - wth the exception of the acrylate resin - are dissolved in alcohol and this solution is added, with stirring, to the hydroxypropyl cellulose. Subsequently, the acrylate resin is added and stirred until completely dissolved.
• Benzophenone-4 is 5-benzoyl-4-hydroxy-2-methoxybenzenesulfonic acid, sodium salt. Excellent results are achieved.
• Example 10 Preparation of a shampoo for qreasy hair
• UV absorber 0.15 phosphonomethylchitosan, sodium salt 0.01 perfume oil 0.10 water ad. 100
• the components are mixed, with stirring, at room temperature until they are completely dissolved.
• the pH is 6.5.
• the UV absorber is one of the present disclosure, for example 2-(2- hydroxy-3-dodecyl-5-methylphenyl)-2H-benzotriazole. Excellent results are achieved.
• Example 11 Preparation of a leather dressing and cleaning agent
• Example 12 Preparation of a glass detergent Ingredients (w/w) % anionic / amphoteric surfactants (Lumorol RK) 0.7 butyl glycol 5.0
• the stabilizer is predissolved in the terpene.
• the components are then dissolved in the cited sequence until a clear homogeneous mixture is obtained. Excellent results are achieved.
• Stabilizers (C), (D) and (E) are each deposited (from water) on a dyed cotton fabric at 0.05, 0.1 , 0.2, 0.5 and 1.0 percent by weight, based on the weight of the cotton.
• the dyed fabrics contain the following dyes at 0.05, 0.1 , 0.2 and 0.5 percent by weight based on cotton. This results in 60 separate formulations for each dye listed:
• the cotton fabrics are subjected to light exposure in an Atlas Ci-65 Xenon arc WetherOmeter and to accelerated fluorescent lighting.
• the present stabilizers provide outstanding color protection to the dyed fabrics. This experiment simulates dye protection achievable through deposition of the present stabilizers via treatment with for example stabilizer-containing laundry detergent or fabric conditioner.

Landscapes

• Life Sciences & Earth Sciences (AREA)
• Health & Medical Sciences (AREA)
• Engineering & Computer Science (AREA)
• Textile Engineering (AREA)
• Animal Behavior & Ethology (AREA)
• General Health & Medical Sciences (AREA)
• Public Health (AREA)
• Veterinary Medicine (AREA)
• Chemical & Material Sciences (AREA)
• Birds (AREA)
• Epidemiology (AREA)
• Oil, Petroleum & Natural Gas (AREA)
• Organic Chemistry (AREA)
• Wood Science & Technology (AREA)
• Chemical Kinetics & Catalysis (AREA)
• Dermatology (AREA)
• Cosmetics (AREA)
• Detergent Compositions (AREA)
• Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
• Details Of Garments (AREA)
• Agricultural Chemicals And Associated Chemicals (AREA)

Priority Applications (10)

Applications Claiming Priority (2)

Publications (1)

Family

ID=29736067

Family Applications (1)

Country Status (13)

Cited By (17)

Families Citing this family (30)

Citations (5)

Family Cites Families (10)

• 2003
  • 2003-04-24 JP JP2004510742A patent/JP4594727B2/ja not_active Expired - Lifetime
  • 2003-04-24 AU AU2003233054A patent/AU2003233054A1/en not_active Abandoned
  • 2003-04-24 AT AT03727349T patent/ATE463228T1/de not_active IP Right Cessation
  • 2003-04-24 EP EP03727349A patent/EP1499286B1/en not_active Expired - Lifetime
  • 2003-04-24 KR KR1020047017595A patent/KR100975789B1/ko not_active Expired - Lifetime
  • 2003-04-24 MX MXPA04010833A patent/MXPA04010833A/es active IP Right Grant
  • 2003-04-24 US US10/512,528 patent/US9358195B2/en active Active
  • 2003-04-24 CN CN038097516A patent/CN1649566B/zh not_active Expired - Lifetime
  • 2003-04-24 WO PCT/EP2003/004262 patent/WO2003103622A1/en not_active Ceased
  • 2003-04-24 ES ES03727349T patent/ES2342594T3/es not_active Expired - Lifetime
  • 2003-04-24 DE DE60332012T patent/DE60332012D1/de not_active Expired - Lifetime
  • 2003-04-24 BR BRPI0309692-0B1A patent/BR0309692B1/pt active IP Right Grant
  • 2003-04-30 TW TW092110122A patent/TWI329519B/zh not_active IP Right Cessation
• 2010
  • 2010-07-01 JP JP2010151413A patent/JP5323771B2/ja not_active Expired - Lifetime

Patent Citations (5)

Also Published As

Similar Documents

Legal Events