EP3860553A1 - Écran solaire éthanolique contenant des alcools gras ayant une tendance réduite à former des taches sur les textiles - Google Patents

Écran solaire éthanolique contenant des alcools gras ayant une tendance réduite à former des taches sur les textiles

Info

Publication number
EP3860553A1
EP3860553A1 EP19769764.2A EP19769764A EP3860553A1 EP 3860553 A1 EP3860553 A1 EP 3860553A1 EP 19769764 A EP19769764 A EP 19769764A EP 3860553 A1 EP3860553 A1 EP 3860553A1
Authority
EP
European Patent Office
Prior art keywords
inci
sunscreen
preparation
bis
diethylamino
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.)
Pending
Application number
EP19769764.2A
Other languages
German (de)
English (en)
Inventor
Lisa Schuldt
Stephanie Von Der Fecht
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.)
Beiersdorf AG
Original Assignee
Beiersdorf AG
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
Application filed by Beiersdorf AG filed Critical Beiersdorf AG
Publication of EP3860553A1 publication Critical patent/EP3860553A1/fr
Pending legal-status Critical Current

Links

Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q17/00—Barrier preparations; Preparations brought into direct contact with the skin for affording protection against external influences, e.g. sunlight, X-rays or other harmful rays, corrosive materials, bacteria or insect stings
    • A61Q17/04—Topical preparations for affording protection against sunlight or other radiation; Topical sun tanning preparations
    • 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
    • A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • A61K8/34—Alcohols
    • 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
    • A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • A61K8/34—Alcohols
    • A61K8/342—Alcohols having more than seven atoms in an unbroken chain
    • 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
    • A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • A61K8/35—Ketones, e.g. benzophenone
    • 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
    • A61K8/415—Aminophenols
    • 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
    • A61K8/494—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with more than one nitrogen as the only hetero atom
    • A61K8/4966—Triazines or their condensed derivatives
    • 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
    • A61K2800/20—Chemical, physico-chemical or functional or structural properties of the composition as a whole
    • A61K2800/26—Optical properties
    • A61K2800/262—Transparent; Translucent

Definitions

  • the present invention relates to an ethanolic cosmetic sunscreen composition
  • UV filters selected from the group of compounds 4- (tert-butyl) -4'- methoxydibenzoylmethane (INCI butyl methoxydibenzoylmethane), (2 - [- 4- (diethylamino) -2-hydroxybenzoyl] benzoic acid hexyl ester ( INCI: Diethylamino Hydroxybenzoyl Hexyl Benzoate) and 2,4-bis - ⁇ [4- (2-ethylhexyloxy) -2-hydroxy] phenyl ⁇ -6- (4-methoxyphenyl) -1, 3,5-triazine ( INCI: bis-ethylhexyloxyphenol methoxyphenyl triazine),
  • UVB range wavelength: 280-320 nm
  • UVA radiation wavelength: 320-400 nm
  • UVA and UVB filters are in most industrialized countries in the form of positive lists such as Appendix 7 of the
  • Cosmetic preparations such as sunscreen preparations which are applied to the skin come into regular contact (intentionally or unintentionally) with items of clothing and laundry items (for example towels) on which they are applied (for example as “abrasion” or because they are “sucked up” by the fibers). partly stick. In this way, depending on the type of ingredients, stains and discolouration occur, especially on light textiles.
  • UVA and broadband filters such as 4- (tert-butyl) -4'-methoxydibenzoylmethane (INCI butyl methoxydibenzoylmethane), (2 - [- 4- (diethylamino) -2-hydroxybenzoylj benzoic acid hexyl ester (INCI: Diethylamino hydroxybenzoyl hexyl benzoate) and 2,4-bis - ⁇ [4- (2-ethylhexyloxy) -2-hydroxy] phenyl ⁇ -6- (4-methoxyphenyl) -1,3,5-triazine (INCI: Bis-ethylhexyloxyphenol methoxyphenyl triazine)
  • Stains can hardly be removed by washing with conventional detergents and intensify during the washing process through interactions with ions of the
  • Methoxydibenzoylmethane (2 - [- 4- (Diethylamino) -2-hydroxybenzoylj benzoic acid hexyl ester (INCI: Diethylamino Hydroxybenzoyl Hexyl Benzoate) and 2,4-bis - ⁇ [4- (2-ethylhexyloxy) -2-hydroxy ] -phenyl ⁇ -6- (4-methoxyphenyl) -1, 3,5-triazine (INCI: bis-ethylhexyloxyphenol methoxyphenyl triazine).
  • an ethanolic, cosmetic sunscreen comprising a) one or more UV filters selected from the group of the compounds 4- (tert-butyl) -4'- methoxydibenzoylmethane (INCI butyl methoxydibenzoylmethane), (2 - [- 4- (diethylamino) -2-hydroxybenzoyl] benzoic acid hexyl ester (INCI: diethylamino hydroxybenzoyl hexyl benzoate) and 2,4-bis - ⁇ [4- (2-ethylhexyloxy) - 2-hydroxy] phenyl ⁇ -6- (4-methoxyphenyl) -1, 3,5-triazine (INCI: bis-ethylhexyloxyphenol methoxyphenyl triazine),
  • Methoxydibenzoylmethane (2 - [- 4- (diethylamino) -2-hydroxybenzoyl] benzoic acid hexyl ester (INCI: diethylamino hydroxybenzoyl hexyl benzoate) and 2,4-bis - ⁇ [4- (2-ethylhexyloxy) -2-hy- droxy] -phenyl ⁇ -6- (4-methoxyphenyl) -1, 3,5-triazine (INCI: bis-ethylhexyloxyphenol methoxyphenyl triazine), to make it easier to wash out the UV light protection filter with the
  • the task is also solved by using fatty alcohols in
  • Methoxydibenzoylmethane (2 - [- 4- (diethylamino) -2-hydroxybenzoyl] benzoic acid hexyl ester (INCI: diethylamino hydroxybenzoyl hexyl benzoate) and 2,4-bis - ⁇ [4- (2-ethylhexyloxy) -2-hy- droxy] -phenyl ⁇ -6- (4-methoxyphenyl) -1, 3,5-triazine (INCI: bis-ethylhexyloxyphenol methoxyphenyl triazine), to reduce the textile stains caused by the sunscreen.
  • the task is solved not least by a process to facilitate the
  • Fatty alcohols can be added.
  • fatty alcohols are understood to be linear, unbranched, long-chain primary alcohols with a carbon chain length of 12 to 30 carbon atoms (definition).
  • the prior art knows DE 102016220547.1 (also published under
  • an “ethanolic sunscreen” is understood to be a sunscreen that contains at least 10% by weight of ethanol, based on the total weight of the preparation. According to the invention, such an ethanolic sunscreen preferably contains from 20 to 75% by weight of ethanol and particularly preferably from 25 to 70% by weight of ethanol, in each case based on the total weight of the preparation.
  • formulations “according to the invention”, “according to the invention advantageously” etc. always refer to the sunscreen according to the invention, the uses according to the invention and the method according to the invention, unless it is described differently in the individual case.
  • fatty alcohols are cetyl alcohol, stearyl alcohol,
  • Behenyl alcohol and / or myristyl alcohol can be used.
  • cetostearyl alcohol cetearyl alcohol
  • cetearyl alcohol cetearyl alcohol
  • the fatty alcohols are present in a total concentration of 0.25% to 10% by weight, based on the total weight of the preparation.
  • the total concentration preferred according to the invention is from 0.5% to 6% by weight, based on the total weight of the preparation.
  • Embodiments of the present invention which are advantageous according to the invention are characterized in that the total concentration of the UV filters 4- (tert-butyl) -4'-methoxydibenzoylmethane (INCI butyl methoxydibenzoylmethane), (2 - [- 4- (diethylamino) - 2-hydroxybenzoyl] benzoic acid hexyl ester (INCI: diethylamino hydroxybenzoyl hexyl benzoate) and 2,4-bis - ⁇ [4- (2-ethylhexyloxy) -2-hydroxy] phenyl ⁇ -6- (4-methoxyphenyl) -1, 3,5-triazine (INCI: bis-ethylhexyloxyphenol methoxyphenyl triazine) in the preparation is from 0.5 to 15% by weight, based on the total weight of the preparation. It is preferred according to the invention if the preparation according to the invention if the preparation according
  • Methoxydibenzoylmethane (2 - [- 4- (diethylamino) -2-hydroxybenzoyl] benzoic acid hexyl ester (INCI: diethylamino hydroxybenzoyl hexyl benzoate) and 2,4-bis - ⁇ [4- (2-ethylhexyloxy) -2-hy- droxy] -phenyl ⁇ -6- (4-methoxyphenyl) -1, 3,5-triazine (INCI: bis-ethylhexyloxyphenol methoxyphenyl triazine) d) (2 - [- 4- (diethylamino) -2-hydroxybenzoyl] benzoic acid hexyl ester (INCI: Diethylamino
  • Methoxydibenzoylmethane from 1.5 to 5% by weight and for bis-ethylhexyloxyphenol
  • Methoxyphenyl triazine from 0.25 to 5% by weight, based in each case on the total weight of the preparation.
  • fatty alcohols myristyl alcohol, cetyl alcohol, cetearyl alcohol, stearyl alcohol are preferred according to the invention
  • the advantageous use concentration according to the invention for diethylamino hydroxybenzoyl hexyl benzoate is from 0.5 to 10% by weight and for bis-ethylhexyloxyphenol methoxyphenyl triazine from 0.25 to 5% by weight, in each case based on the total weight of the preparation.
  • the fatty alcohols myristyl alcohol, cetyl alcohol, cetearyl alcohol, stearyl alcohol are preferably used in a concentration of 0.25 to 10% by weight, based on the total weight of the preparation.
  • the advantageous use concentration for butyl is according to the invention
  • Methoxydibenzoylmethane from 0.6 to 5% by weight, for diethylamino hydroxybenzoyl hexyl benzoate from 0.5 to 4.9% by weight and for bis-ethylhexyloxyphenol methoxyphenyl triazine from 0.25 to 5% by weight, each based on the total weight of the Preparation.
  • the fatty alcohols myristyl alcohol, cetyl alcohol, cetearyl alcohol, stearyl alcohol are preferably used in a concentration of 0.25 to 10% by weight, based on the total weight of the preparation.
  • the advantageous use concentration according to the invention for diethylamino hydroxybenzoyl hexyl benzoate is from 0.5 to 10% by weight based on the total weight of the preparation.
  • Advantageous embodiments of the present invention are characterized in that the ethanol content of the preparation is from 25 to 70% by weight, based on the total weight of the preparation.
  • a preparation is considered transparent if it is possible for
  • the preparation does not contain a 3- (4-methylbenzylidene) camphor, 2-hydroxy-4-methoxybenzophenone (INCI: oxybenzone), phenylene-1,4-bis- (2-benzimidazyl) -3,3'-5,5'-tetrasulfonic acid salts; 1, 4-di (2-oxo-10-sulfo-3-bornylidene-methyl) -benzene and its salts; 4- (2-oxo-3-bornylidenemethyl) benzenesulfonic acid salts; 2-methyl-5- (2-oxo-3-bornylidene methyl) sulfonic acid salts, 3-benzylidene camphor;
  • Terephthalic dicampher sulfonic acid 4- (dimethylamino) benzoic acid (2-ethylhexyl) ester; 4-methoxybenzalmalonic acid di (2-ethylhexyl) ester; Contains 4-methoxycinnamic acid isoamyl ester and 4-methoxycinnamic acid ethylhexyl ester, so it is free of these ingredients.
  • the preparation contains 2-ethylhexyl 2-hydroxybenzoate (INCI: ethylhexyl salicylate) and / or 3,3, 5-trimethylcyclohexyl 2-hydroxybenzoate (INCI: homosalate).
  • preparation according to the invention contains 2-ethylhexyl 2-hydroxybenzoate, its advantageous use concentration according to the invention is from 2.5 to 9% by weight, based on the total weight of the preparation.
  • the preparation according to the invention contains 3,3,5-trimethylcyclohexyl 2-hydroxybenzoate, its advantageous use concentration according to the invention is from 3 to 10% by weight, based on the total weight of the preparation.
  • Embodiments of the present invention which are advantageous according to the invention are characterized in that the preparation is free from ethylhexyl-2-cyano-3,3-diphenylacrylate (INCI: octocrylene). In addition, it is advantageous according to the invention if the preparation according to the invention does not contain octyldodecanol.
  • Embodiments of the present invention which are advantageous according to the invention are characterized in that the preparation comprises one or more perfume substances selected from the group consisting of the compounds limonene, citral, linalool, alpha-isomethylionone, geraniol, citronellol, 2-isobutyl-4-hydroxy-4-methyltetrahydropyran, 2 -tert-pentylcyclohexyl acetate, 3-methyl-5-phenyl-1-pentanol, 7-acetyl-1, 1, 3,4,4,6-hexamethyltetralin, adipic acid diester, alpha-amylcinnamaldehyde, alpha-methylionone, amyl C butylphenylmethylpropionalcinnamal,
  • the preparation contains acrylates / octylacrylamides copolymer.
  • the advantageous amount according to the invention is
  • the preparation according to the invention contains less than 3.0% by weight of water, based on the total weight of the preparation.
  • Cocoglyceride (INCI Cocoglycerides), Caprylic / Capric Triglyceride (INCI: Caprylic / Capric Triglyceride), C12-15 Contains alkyl benzoate, di-n-butyl adipate and / or butylene glycol dicaprylate / dicaprate (INCI: Butylene Glycol Dicaprylate / Dicaprate).
  • test formulas are applied to the stain monitors using PMMA plates (3 mg / cm 2 ). Four spots are created per formula.
  • the stains are left to dry overnight.
  • the l * , a * and b * values are measured as in 1) and the staining (in particular the b * value) is calculated before or after the washing process.

Landscapes

  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Birds (AREA)
  • Epidemiology (AREA)
  • Emergency Medicine (AREA)
  • Dermatology (AREA)
  • Cosmetics (AREA)

Abstract

La présente invention concerne un écran solaire cosmétique éthanolique contenant a) un ou plusieurs filtres UV choisis dans le groupe des composés 4-(butyle tertiaire)-4'-méthoxydibenzoylméthane (INCI : Butyl Methoxydibenzoylmethane), (2-[-4-(diéthylamino)-2-hydroxybenzoyl] benzoate de diéthylaminohydroxybenzoyle (INCI : Diethylamino Hydroxybenzoyl Hexyl Benzoate) et 2,4-bis-{[4-(2-éthyl-hexyloxy)-2-hydroxy]-phényl}-6-(4-méthoxyphényl)-1,3,5-triazine (INCI : Bis-Ethylhexyloxyphenol Methoxyphenyl Triazine), b) de l'éthanol dans une quantité minimale de 10 % massiques, par rapport au poids total de la préparation, c) un ou plusieurs alcools gras, ainsi que l'utilisation de ces alcools gras pour réduire les taches sur les textiles causées par l'écran solaire.
EP19769764.2A 2018-10-01 2019-09-13 Écran solaire éthanolique contenant des alcools gras ayant une tendance réduite à former des taches sur les textiles Pending EP3860553A1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE102018216823.7A DE102018216823A1 (de) 2018-10-01 2018-10-01 Fettalkohol-haltiges, ethanolisches Sonnenschutzmittel mit reduzierter Neigung zur Textilverfleckung
PCT/EP2019/074493 WO2020069838A1 (fr) 2018-10-01 2019-09-13 Écran solaire éthanolique contenant des alcools gras ayant une tendance réduite à former des taches sur les textiles

Publications (1)

Publication Number Publication Date
EP3860553A1 true EP3860553A1 (fr) 2021-08-11

Family

ID=67988981

Family Applications (1)

Application Number Title Priority Date Filing Date
EP19769764.2A Pending EP3860553A1 (fr) 2018-10-01 2019-09-13 Écran solaire éthanolique contenant des alcools gras ayant une tendance réduite à former des taches sur les textiles

Country Status (3)

Country Link
EP (1) EP3860553A1 (fr)
DE (1) DE102018216823A1 (fr)
WO (1) WO2020069838A1 (fr)

Family Cites Families (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP4671222B2 (ja) 2005-03-16 2011-04-13 株式会社資生堂 皮膚外用剤
US8822547B2 (en) 2007-10-30 2014-09-02 Gojo Industries, Inc. Hydroalcoholic gel compositions for use with dispensers
DE102010008320A1 (de) * 2010-02-17 2011-08-18 Beiersdorf AG, 20253 Verwendung von Stoffen zur Verbesserung der Auswaschbarkeit von durch UV-Filtern verursachten Textilflecken
CA2834035C (fr) * 2011-04-27 2018-12-18 Isp Investments Inc. Pulverisations humides et gels clairs
FR2976178B1 (fr) 2011-06-09 2013-09-27 Oreal Creme anhydre solaire comprenant un organopolysiloxane elastomere non emulsionnant, un agent matifiant, un epaississant organique non silicone d'huile
US9526925B2 (en) * 2012-05-17 2016-12-27 Edgewell Personal Care Brands, Llc Viscous alcohol-containing sunscreen compositions
DE102013215831A1 (de) 2013-08-09 2015-02-12 Beiersdorf Ag Gelförmiges, alkoholisches Sonnenschutzmittel
DE102015208869A1 (de) * 2015-05-13 2016-11-17 Beiersdorf Ag Alkoholhaltiges, octocrylenfreies Sonnenschutzmittel
DE102016202334A1 (de) 2016-02-16 2017-08-17 Zf Friedrichshafen Ag Unterbaugruppe für eine Antriebseinheit, Antriebseinheit, Antriebsstrangprüfstand und Baukastensystem
DE102016211238A1 (de) * 2016-06-23 2017-12-28 Beiersdorf Ag Sonnenschutzmittel mit reduzierter Textilverfleckung
DE102016220547A1 (de) 2016-10-20 2018-04-26 Beiersdorf Ag Ethanolisches Sonnenschutzmittel mit reduzierter Neigung zur Textilverfleckung
FR3060997B1 (fr) 2016-12-23 2019-05-31 L'oreal Composition comprenant de la baicaline
FR3073400A1 (fr) 2017-11-15 2019-05-17 L'oreal Emulsion cosmetique contenant un tensioactif gemine et un polymere lipophile

Also Published As

Publication number Publication date
DE102018216823A1 (de) 2020-04-02
WO2020069838A1 (fr) 2020-04-09

Similar Documents

Publication Publication Date Title
EP3335691B1 (fr) Préparation anti-solaire contenant des polysaccharides présentant une tendance réduite à tâcher les tissus
WO2011101250A1 (fr) Utilisation de substances pour améliorer la possibilité de suppression des taches produites par des filtres uv sur des textiles
EP3153151B1 (fr) Produit de protection solaire ayant une tendance réduite à former des taches causé par 4-(tert.-butyl)-4 - methoxydibenzoylmethansur les textiles
EP3417844B1 (fr) Préparation d'écran solaire à tendance réduite à la formation de taches sur les textiles iv
EP3311791B1 (fr) Inhibiteur de lumière éthanolique présentant une tendance réduite à tâcher les tissus
EP3137044A1 (fr) Produit de protection solaire ayant une tendance réduite à former des taches sur les textiles ii
EP3228299B1 (fr) Protection solaire ayant une tendance réduite à tâcher les tissus
EP3354253B1 (fr) Utilisation de diéthylamino hydroxybenzoyl hexyl benzoate dans les produits anti-solaire cosmétiques
DE102014206156A1 (de) Sonnenschutzmittel mit verkapselten UV-Filtern III
WO2015165711A1 (fr) Produit de protection solaire ayant une tendance réduite à former des taches sur les textiles i
WO2019170363A1 (fr) Agent de protection solaire ayant une tendance réduite à former des taches sur les textiles et contenant de l'huile végétale hydrogénée et une combinaison de filtre uv composée d'éthylhexyl triazone et de 4-(tert.-butyl)-4'-méthoxydibenzoylméthane
EP3378537B1 (fr) Agent photoprotecteur contenant du triacontanyl pvp
EP2485806B1 (fr) Utilisation de cétéarylsulfosuccinates dans des préparations cosmétiques de protection solaire
EP3761948B1 (fr) Agent de protection solaire ayant une tendance réduite à former des taches sur les textiles et contenant de l'huile végétale hydrogénée et des diéthylamino hydroxybenzoyl hexyl benzoates
EP3860553A1 (fr) Écran solaire éthanolique contenant des alcools gras ayant une tendance réduite à former des taches sur les textiles
EP3723707A1 (fr) Produit de protection solaire à tendance réduite à former des taches sur les textiles
EP3651725A1 (fr) Produit de protection solaire avec protection contre l'apparition de taches dues à la 2,4-bis-{[4-(2-éthyl-hexyl-oxy)-2-hydroxy]-phényl}-6-(4-méthoxyphényl)-1,3,5-triazine sur les textiles
WO2019170361A1 (fr) Agent de protection solaire ayant une tendance réduite à former des taches sur les textiles et contenant de l'huile végétale hydrogénée et des bis-éthylhexyloxyphénol méthoxyphényl triazines
EP3600564B1 (fr) Produit de protection solaire contenant du polyglycéryl-10-stéarate et du citronellol
DE102017204793A1 (de) Sonnenschutzmittel mit Polyglyceryl-10 Stearat und Polyclyceryl-2 Caprat
EP3600565B1 (fr) Produit de protection solaire contenant du polyglycéryl-10-stéarate et du linalol
DE102017212018A1 (de) Sonnenschutzmittel mit Schutz vor Textilverfleckung durch Hexyl 2-[4-(diethylamino)-2-hydroxybenzoyl]benzoate

Legal Events

Date Code Title Description
STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: UNKNOWN

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: THE INTERNATIONAL PUBLICATION HAS BEEN MADE

PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: REQUEST FOR EXAMINATION WAS MADE

17P Request for examination filed

Effective date: 20210503

AK Designated contracting states

Kind code of ref document: A1

Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR

RAP3 Party data changed (applicant data changed or rights of an application transferred)

Owner name: BEIERSDORF AG

DAV Request for validation of the european patent (deleted)
DAX Request for extension of the european patent (deleted)
TPAC Observations filed by third parties

Free format text: ORIGINAL CODE: EPIDOSNTIPA

RAP3 Party data changed (applicant data changed or rights of an application transferred)

Owner name: BEIERSDORF AG