WO2012019689A2 - Verwendung von hydroxypyridonen oder deren salzen zur stabilisierung von wasserstoffperoxid oder wasserstoffperoxid freisetzenden substanzen - Google Patents

Verwendung von hydroxypyridonen oder deren salzen zur stabilisierung von wasserstoffperoxid oder wasserstoffperoxid freisetzenden substanzen Download PDF

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Publication number
WO2012019689A2
WO2012019689A2 PCT/EP2011/003537 EP2011003537W WO2012019689A2 WO 2012019689 A2 WO2012019689 A2 WO 2012019689A2 EP 2011003537 W EP2011003537 W EP 2011003537W WO 2012019689 A2 WO2012019689 A2 WO 2012019689A2
Authority
WO
WIPO (PCT)
Prior art keywords
hydrogen peroxide
component
use according
salts
substances
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Ceased
Application number
PCT/EP2011/003537
Other languages
German (de)
English (en)
French (fr)
Other versions
WO2012019689A3 (de
Inventor
Peter Klug
Maurice Frederic Pilz
Ute Back
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Clariant International Ltd
Original Assignee
Clariant International Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority claimed from DE201010054865 external-priority patent/DE102010054865A1/de
Application filed by Clariant International Ltd filed Critical Clariant International Ltd
Priority to ES11740562.1T priority Critical patent/ES2525388T3/es
Priority to CN201180036428.6A priority patent/CN103118973B/zh
Priority to BR112013001953A priority patent/BR112013001953A2/pt
Priority to EP11740562.1A priority patent/EP2598436B1/de
Priority to US13/812,114 priority patent/US9090467B2/en
Priority to JP2013521004A priority patent/JP5901076B2/ja
Publication of WO2012019689A2 publication Critical patent/WO2012019689A2/de
Publication of WO2012019689A3 publication Critical patent/WO2012019689A3/de
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C01—INORGANIC CHEMISTRY
    • C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B15/00—Peroxides; Peroxyhydrates; Peroxyacids or salts thereof; Superoxides; Ozonides
    • C01B15/01—Hydrogen peroxide
    • C01B15/037—Stabilisation by additives
    • 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
    • A61K8/19—Cosmetics or similar toiletry preparations characterised by the composition containing inorganic ingredients
    • A61K8/22—Peroxides; Oxygen; Ozone
    • 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
    • A61Q5/00—Preparations for care of the hair
    • A61Q5/08—Preparations for bleaching 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
    • A61Q5/10—Preparations for permanently dyeing the hair
    • C—CHEMISTRY; METALLURGY
    • C01—INORGANIC CHEMISTRY
    • C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B15/00—Peroxides; Peroxyhydrates; Peroxyacids or salts thereof; Superoxides; Ozonides
    • C01B15/055—Peroxyhydrates; Peroxyacids or salts thereof
    • C01B15/06—Peroxyhydrates; Peroxyacids or salts thereof containing sulfur
    • C01B15/08—Peroxysulfates
    • C01B15/085—Stabilisation of the solid compounds, subsequent to the preparation or to the crystallisation, by additives or by coating
    • C—CHEMISTRY; METALLURGY
    • C01—INORGANIC CHEMISTRY
    • C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B15/00—Peroxides; Peroxyhydrates; Peroxyacids or salts thereof; Superoxides; Ozonides
    • C01B15/055—Peroxyhydrates; Peroxyacids or salts thereof
    • C01B15/12—Peroxyhydrates; Peroxyacids or salts thereof containing boron
    • C01B15/123—Stabilisation of the solid compounds, subsequent to the preparation or to the crystallisation, by additives or by coating
    • 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
    • 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 hydroxypyridones or their salts for the stabilization of hydrogen peroxide or hydrogen peroxide releasing substances.
  • Compositions, and particularly aqueous compositions containing hydrogen peroxide are used in various applications. They are used in cosmetic products z. B. used as a bleaching composition for hair, as a developer component in hair dyes, but also as a component for hair fixation in permanent wave formulations. Other applications are z. B. tooth whitening compositions. Also in industrial cleaning and household cleaning and in textile bleaching are hydrogen peroxide-containing compositions represented.
  • the invention thus relates to the use of one or more
  • Hydrogen peroxide-releasing substances (component a)).
  • the one or more substances selected from the group consisting of hydroxypyridones and their salts are also referred to as substances of component d).
  • the one or more substances selected from the group consisting of hydrogen peroxide and hydrogen peroxide-releasing substances are hereinafter also referred to as substances of component a).
  • the hydrogen peroxide and / or the hydrogen peroxide-releasing substances are stabilized whereby, for example, the storage stability of corresponding compositions is increased. Due to the increased stability of the hydrogen peroxide and / or the
  • Hydrogen peroxide-releasing substances in these compositions either the effect of the ingredients can be increased, such as. B. their cleaning or bleaching performance, or the useful life of such formulations can be increased.
  • EP 1 347 736 describes oxidative compositions for hair treatment which contain stabilizers for hydrogen peroxide based on pyrophosphate, stannates, phenacetin or oxyquinoline or combinations thereof.
  • the one or more substances of component a) is selected from the group consisting of hydrogen peroxide, urea peroxide, perborates, persulfates and mixtures thereof.
  • the substance of component a) is particularly preferably hydrogen peroxide.
  • the one or more substances of component d) are selected from compounds of formula (I) and their salts wherein R 1 is H or a C 1 -C 4 alkyl radical and R 2 is H, an unsubstituted or halogen-substituted, branched or unbranched C 1 -C 20 alkyl radical, an unsubstituted or halogen-substituted C 5 -C 8 cycloalkyl radical
  • radicals R2 are not substituted by halogen.
  • the one or more compounds of component d) is in the form of the acid (compounds of the formula (I)) or in the form of their alkali, alkaline earth or amine salts or their salts with polymeric counterions.
  • R 1 is preferably methyl and R 2 is preferably cyclohexyl or
  • Alkanolamine salts and particularly preferably in the form of their
  • 4-methyl-6- (2,4,4-trimethylpentyl) -1-hydroxy-2-pyridone the monoethanolamine salt of 4-methyl-6- (2,4,4-trimethylpentyl) -1-hydroxy -2-pyridone (octopirox ®, Clariant) and 4-methyl-6- (cyclohexyl) -1-hydroxy- 2-pyridone and monoethanolamine salt of 4-methyl-6- (cyclohexyl) -1-hydroxy-2-pyridone (Ciclopirox ®, Sanofi-Aventis).
  • the use according to the invention is in aqueous
  • the water is contained in an amount of 40% by weight or more, and more preferably in an amount of 50% by weight or more in the aqueous compositions, based on the total weight of the aqueous compositions.
  • the one or more substances selected from the group consisting of hydrogen peroxide and hydrogen peroxide-releasing substances of component a) are preferably in amounts of 0.5 to 20 wt .-%, particularly preferably in amounts of 1 to 10 wt .-%, in particular preferably in amounts of 1, 5 to 7 wt .-% and most preferably in amounts of 2 to
  • the substance of component a) is preferably hydrogen peroxide, which is preferably present in amounts of from 0.5 to 20% by weight, more preferably in amounts of from 1 to 10% by weight, particularly preferably in amounts of from 1.5 to 7 Wt .-% and most preferably in amounts of 2 to 7 wt .-% in the aqueous compositions, based on the total weight of the aqueous compositions.
  • the one or more of component d) is in amounts of preferably 0.1 to 20,000 ppm (0.00001 to 2% by weight), more preferably in amounts of 0.5 to 1,000 ppm (0.00005 to 0.1% by weight) and most preferably in amounts of 0.5 to 100 ppm (0.00005 to 0.01% by weight) based on the total weight of the aqueous compositions.
  • hydroxypyridones or their salts can be used in the inventive
  • stabilizers are, for. As polyphosphates or their alkali or
  • Alkaline earth metal salts alkali or Erdalkalistannate, phenacetin and its
  • aqueous compositions may be used as further auxiliaries and additives oil body, silicone oils, waxes, surfactants, emulsifiers, co-emulsifiers,
  • Solubilizers cationic polymers, film formers, superfatting agents, refatting agents, antimicrobial agents, humectants, solvents, dyes, fragrances, pearlescing agents and / or opacifiers.
  • the aqueous compositions may contain organic solvents.
  • organic solvents In principle, all mono- or polyhydric alcohols are suitable as organic solvents. Alcohols having 1 to 4 carbon atoms such as ethanol, propanol, isopropanol, n-butanol, i-butanol, t-butanol, glycerol, 1, 2- and 1, 3-propanediol and mixtures of the alcohols mentioned are preferred
  • Further preferred alcohols are polyethylene glycols with a molecular weight below 2,000.
  • use of polyethylene glycols with a molecular weight below 2,000.
  • Polyethylene glycol having a molecular weight between 200 and 600 and in amounts up to 45.0 wt .-% and of polyethylene glycol with a relative
  • Molecular weight between 400 and 600 in amounts of 5.0 to 25.0 wt .-% is preferred.
  • Other suitable solvents include triacetin
  • the aqueous compositions may, for. B. also aqueous surfactant or aqueous-alcoholic compositions or emulsions. As acids or alkalis for the pH adjustment of the aqueous
  • Compositions are preferably mineral acids, especially HCl, inorganic bases, especially NaOH or KOH, and organic acids, especially citric acid.
  • the aqueous compositions have a pH of from 2 to 11, more preferably from 7 to 11, more preferably from 8 to 11, and most preferably from 8.5 to 11.
  • Hydrogen peroxide-releasing substances may, for. B. at the following
  • Hydrogen peroxide or hydrogen peroxide-releasing substances as fixing component for permanent wave formulations in household cleaners, in oxidative detergent formulations, in compositions for the oxidative bleaching of fibers or textiles, in pre-wash sprays, stain removers,
  • Solvay hydrogen peroxide solution (35% by weight in water) or Merck (35% by weight in water) was diluted to a hydrogen peroxide content of about 6.0% by weight with demineralized water and washed with sodium hydroxide solution (20% by weight). %) to a pH of 9.0. Further solutions were each additivert with 8 ppm of 4-methyl-6- (2,4,4-trimethylpentyl) -1-hydroxy-2-pyridone (additive A, dissolved in propylene glycol). The solutions were incubated at room temperature (20 ° C) and Stored at 40 ° C for 1 week and the hydrogen peroxide content measured before and after storage (see Table 1).
  • Hydrogen peroxide solution of Solvay (35 wt .-% in water) or Merck (35 wt .-% in water), a solution of sodium C -17 alkyl sec. Sulfonates (Hostapur ® SAS 30) and demineralized water were mixed in that a hydrogen peroxide content of about 6.0% by weight and a content of sodium
  • trimethylpentyl) -1-hydroxy-2-pyridone both at room temperature and at 40 ° C can significantly increase the storage stability of hydrogen peroxide solutions at high pH.
  • Example 3 Hydrogen peroxide gel thickened with a sulfonate polymer

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Inorganic Chemistry (AREA)
  • Veterinary Medicine (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Birds (AREA)
  • Epidemiology (AREA)
  • Emergency Medicine (AREA)
  • Cosmetics (AREA)
  • Detergent Compositions (AREA)
  • Pyridine Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
PCT/EP2011/003537 2010-07-27 2011-07-15 Verwendung von hydroxypyridonen oder deren salzen zur stabilisierung von wasserstoffperoxid oder wasserstoffperoxid freisetzenden substanzen Ceased WO2012019689A2 (de)

Priority Applications (6)

Application Number Priority Date Filing Date Title
ES11740562.1T ES2525388T3 (es) 2010-07-27 2011-07-15 Utilización de hidroxipiridonas o de sus sales para la estabilización del peróxido de hidrógeno o de unas sustancias que ponen en libertad peróxido de hidrógeno
CN201180036428.6A CN103118973B (zh) 2010-07-27 2011-07-15 羟基吡啶酮或其盐用于稳定化过氧化氢或释放过氧化氢的物质的用途
BR112013001953A BR112013001953A2 (pt) 2010-07-27 2011-07-15 uso de hidroxipiridonas ou sais dos mesmos para a estabilização de peróxido de hidrogênio ou substâncias doadoras de peróxido de hidrogênio
EP11740562.1A EP2598436B1 (de) 2010-07-27 2011-07-15 Verwendung von hydroxypyridonen oder deren salzen zur stabilisierung von wasserstoffperoxid oder wasserstoffperoxid freisetzenden substanzen
US13/812,114 US9090467B2 (en) 2010-07-27 2011-07-15 Method of stabilizing hydrogen peroxide or hydrogen peroxide donor substances with hydroxypyridones or salts therof
JP2013521004A JP5901076B2 (ja) 2010-07-27 2011-07-15 過酸化水素又は過酸化水素遊離物質を安定化するためのヒドロキシピリドン類又はそれらの塩の使用

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
DE102010032371 2010-07-27
DE102010032371.3 2010-07-27
DE201010054865 DE102010054865A1 (de) 2010-12-17 2010-12-17 Verwendung von Hydroxypyridonen oder deren Salzen zur Stabilisierung von Wasserstoffperoxid oder Wasserstoffperoxid freisetzenden Substanzen
DE102010054865.0 2010-12-17

Publications (2)

Publication Number Publication Date
WO2012019689A2 true WO2012019689A2 (de) 2012-02-16
WO2012019689A3 WO2012019689A3 (de) 2012-05-24

Family

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Family Applications (1)

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PCT/EP2011/003537 Ceased WO2012019689A2 (de) 2010-07-27 2011-07-15 Verwendung von hydroxypyridonen oder deren salzen zur stabilisierung von wasserstoffperoxid oder wasserstoffperoxid freisetzenden substanzen

Country Status (7)

Country Link
US (1) US9090467B2 (enExample)
EP (1) EP2598436B1 (enExample)
JP (1) JP5901076B2 (enExample)
CN (1) CN103118973B (enExample)
BR (1) BR112013001953A2 (enExample)
ES (1) ES2525388T3 (enExample)
WO (1) WO2012019689A2 (enExample)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
MX2013001095A (es) 2010-07-27 2013-03-12 Clariant Finance Bvi Ltd Composiciones que comprenden peroxido de hidrogeno o sustancias donadoras de peroxido de hidrogeno.
DE102010054866A1 (de) 2010-12-17 2011-08-18 Clariant International Ltd. Zusammensetzungen enthaltend Wasserstoffperoxid oder Wasserstoffperoxid freisetzende Substanzen
EP3288533B1 (de) * 2015-04-28 2020-08-19 Basf Se Verwendung einer zusammensetzung zum bleichen von zähnen
JP6650158B1 (ja) * 2019-03-29 2020-02-19 株式会社Ｋｏｒｔｕｃ 過酸化水素の保存を安定させるためのオイル組成物
CN108956597B (zh) * 2018-08-30 2021-12-17 广州市默孚材料科技有限公司 一种等离子体灭菌指示试纸
AU2020254639B2 (en) 2019-03-29 2023-05-11 Kortuc Inc. Hydrogen peroxide solution-prefilled syringe having excellent hydrogen peroxide preservability by virtue of silicone oil (oil composition containing said silicone oil)

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DE2234009A1 (de) 1972-07-11 1974-01-24 Hoechst Ag Kosmetische zubereitungen
EP1347736A1 (fr) 2000-12-22 2003-10-01 L'oreal Composition oxydante pour le traitement des matieres keratiniques a base de polymeres amphiphiles d'au moins un monomere a insaturation ethylenique a groupement sulfonique et comportant une partie hydrophobe

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JP2959873B2 (ja) * 1991-05-24 1999-10-06 大日本除蟲菊株式会社 アルカリ性過酸化水素水溶液及びその安定化方法
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PT768302E (pt) * 1995-09-29 2005-11-30 Novartis Ag Novas hidroxipiridinonas
FR2753372B1 (fr) 1996-09-17 1998-10-30 Oreal Composition oxydante gelifiee et utilisations pour la teinture, pour la deformation permanente ou pour la decoloration des cheveux
US5997764A (en) 1997-12-04 1999-12-07 The B.F. Goodrich Company Thickened bleach compositions
DE19802708A1 (de) * 1998-01-24 1999-07-29 Hoechst Marion Roussel De Gmbh Verwendung von hydroxypyridon-haltigen Puderzubereitungen zur Behandlung von Unterschenkel- und Druckgeschwüren
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DE102010054918A1 (de) 2010-12-17 2011-06-30 Clariant International Ltd. Zusammensetzungen enthaltend Wasserstoffperoxid oder Wasserstoffperoxid freisetzende Substanzen
MX2013001095A (es) 2010-07-27 2013-03-12 Clariant Finance Bvi Ltd Composiciones que comprenden peroxido de hidrogeno o sustancias donadoras de peroxido de hidrogeno.
DE102010054866A1 (de) 2010-12-17 2011-08-18 Clariant International Ltd. Zusammensetzungen enthaltend Wasserstoffperoxid oder Wasserstoffperoxid freisetzende Substanzen

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Publication number Priority date Publication date Assignee Title
DE2234009A1 (de) 1972-07-11 1974-01-24 Hoechst Ag Kosmetische zubereitungen
EP1347736A1 (fr) 2000-12-22 2003-10-01 L'oreal Composition oxydante pour le traitement des matieres keratiniques a base de polymeres amphiphiles d'au moins un monomere a insaturation ethylenique a groupement sulfonique et comportant une partie hydrophobe

Also Published As

Publication number Publication date
US9090467B2 (en) 2015-07-28
US20130236383A1 (en) 2013-09-12
EP2598436B1 (de) 2014-09-24
JP5901076B2 (ja) 2016-04-06
ES2525388T3 (es) 2014-12-23
JP2013535391A (ja) 2013-09-12
CN103118973A (zh) 2013-05-22
BR112013001953A2 (pt) 2018-05-15
CN103118973B (zh) 2016-03-23
EP2598436A2 (de) 2013-06-05
WO2012019689A3 (de) 2012-05-24

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