[go: up one dir, main page]

EP2950678A1 - Haarfärbekit - Google Patents

Haarfärbekit

Info

Publication number
EP2950678A1
EP2950678A1 EP14701170.4A EP14701170A EP2950678A1 EP 2950678 A1 EP2950678 A1 EP 2950678A1 EP 14701170 A EP14701170 A EP 14701170A EP 2950678 A1 EP2950678 A1 EP 2950678A1
Authority
EP
European Patent Office
Prior art keywords
amino
diamine
container
benzene
kit
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
EP14701170.4A
Other languages
English (en)
French (fr)
Inventor
Ross David ASHTON
Andrew David Wyrko
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.)
Unilever PLC
Unilever NV
Original Assignee
Unilever PLC
Unilever NV
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 Unilever PLC, Unilever NV filed Critical Unilever PLC
Priority to EP14701170.4A priority Critical patent/EP2950678A1/de
Publication of EP2950678A1 publication Critical patent/EP2950678A1/de
Ceased legal-status Critical Current

Links

Classifications

    • AHUMAN NECESSITIES
    • A45HAND OR TRAVELLING ARTICLES
    • A45DHAIRDRESSING OR SHAVING EQUIPMENT; EQUIPMENT FOR COSMETICS OR COSMETIC TREATMENTS, e.g. FOR MANICURING OR PEDICURING
    • A45D19/00Devices for washing the hair or the scalp; Similar devices for colouring the hair
    • AHUMAN NECESSITIES
    • A45HAND OR TRAVELLING ARTICLES
    • A45DHAIRDRESSING OR SHAVING EQUIPMENT; EQUIPMENT FOR COSMETICS OR COSMETIC TREATMENTS, e.g. FOR MANICURING OR PEDICURING
    • A45D34/00Containers or accessories specially adapted for handling liquid toiletry or cosmetic substances, e.g. perfumes
    • AHUMAN NECESSITIES
    • A45HAND OR TRAVELLING ARTICLES
    • A45DHAIRDRESSING OR SHAVING EQUIPMENT; EQUIPMENT FOR COSMETICS OR COSMETIC TREATMENTS, e.g. FOR MANICURING OR PEDICURING
    • A45D19/00Devices for washing the hair or the scalp; Similar devices for colouring the hair
    • A45D19/012Devices for colouring or bleaching separated strands of hair, e.g. highlighting
    • AHUMAN NECESSITIES
    • A45HAND OR TRAVELLING ARTICLES
    • A45DHAIRDRESSING OR SHAVING EQUIPMENT; EQUIPMENT FOR COSMETICS OR COSMETIC TREATMENTS, e.g. FOR MANICURING OR PEDICURING
    • A45D19/00Devices for washing the hair or the scalp; Similar devices for colouring the hair
    • A45D19/0041Processes for treating the hair of the scalp
    • A45D19/0066Coloring or bleaching
    • AHUMAN NECESSITIES
    • A45HAND OR TRAVELLING ARTICLES
    • A45DHAIRDRESSING OR SHAVING EQUIPMENT; EQUIPMENT FOR COSMETICS OR COSMETIC TREATMENTS, e.g. FOR MANICURING OR PEDICURING
    • A45D2200/00Details not otherwise provided for in A45D
    • A45D2200/05Details of containers
    • A45D2200/058Means for mixing different substances prior to application
    • AHUMAN NECESSITIES
    • A45HAND OR TRAVELLING ARTICLES
    • A45DHAIRDRESSING OR SHAVING EQUIPMENT; EQUIPMENT FOR COSMETICS OR COSMETIC TREATMENTS, e.g. FOR MANICURING OR PEDICURING
    • A45D2200/00Details not otherwise provided for in A45D
    • A45D2200/25Kits

Definitions

  • the present invention relates to a kit for dyeing of keratin fibres, in particular human keratin fibres such as the hair.
  • WO 1 1/099485 / EP 2 535 036A discloses a kit for dyeing or bleaching hair comprising a first part, a second part, a thickening composition, and an openable and closable airtight container for mixing.
  • WO 06/066670 / US 2007/0205129 discloses a dish for mixing hair treatment agents, particularly hair colouring products.
  • the present invention is concerned with a kit for colouring hair in which the per- oxygen containing composition is contained in a pot. Study of consumers has shown that they prefer to apply the colouring product using two hands and as such need a steady container that does not need to be held during application of the product. The containers described above do not enable the consumer to apply the colouring product to the hair in this manner. Summary of the Invention
  • the present invention related to a kit for colouring hair comprising: i) a first container containing a composition comprising an oxidative dye; and ii) a second container containing a composition comprising a per-oxygen
  • the second container comprises sides of height X mm, a first end closed by a bottom of external diameter Y mm and a second end opposite the first, having a opening of internal diameter Z mm in which the ratio of X to Y is less than 1 :1 and the internal diameter Z mm differs by 15% or less from the external diameter Ymm and in which internal diameter Z mm is from 60 to 80mm.
  • the invention also relates to a method of colouring the hair using the kit described above comprising the following steps: i) adding the contents of the first container to the second container;
  • the second container containing comprises sides of height X mm, a first end closed by a bottom of external diameter Y mm and a second end opposite to the first, having a opening of internal diameter Z mm in which the ratio of height X mm to external diameter Y mm is less than 1 :1 ; preferably the in which ratio of the height X mm to external diameter Y mm of the second container is from 4:5 to 1 :2.
  • the internal diameter Z mm is from 60 to 80mm, more preferably from 65 to 75 mm and differs by 15% or less from the length of the external diameter Ymm.
  • the height X mm of the second container is from 45 to 65 mm; more preferably from 50 to 60mm.
  • the second container is has a volume from 100 to 300 ml, more preferably from 180 to 260 ml.
  • the second container comprises a rigid casing in which the casing comprises polypropylene(PP), polyethylene (PE), or combinations thereof.
  • the sides of the second container narrow below the opening to form a neck within the container.
  • a lip is formed within the second container which facilitates removal of excess composition from the fingers.
  • At least one part of the second container is deformable, this allows for gas formation within the container to be accommodated without rupture of the container.
  • a preferred embodiment, especially to aid deformation of the container is that the bottom of the second container is domed.
  • the container is preferably cylindrical.
  • the sides of the cylindrical container taper towards the bottom of the container; preferably the sides taper in a curved manner towards the bottom of the container.
  • the second container further comprises a lid.
  • the lid is used to seal the opening.
  • the outer surface of the neck of the container has a screw thread which interacts with a corresponding screw thread of the lid.
  • the oxidizing composition comprises a material capable of producing pero- oxygen, preferably the material is an inorganic peroxygen material capable of yielding hydrogen peroxide in an aqueous medium and include, but are not limited to: hydrogen peroxide; inorganic alkali metal peroxides (e.g. sodium periodate and sodium peroxide); organic peroxides (e.g. urea peroxide, melamine peroxide); inorganic perhydrate salt bleaching compounds (e.g.
  • the per oxygen generating material is hydrogen peroxide.
  • the level of per-oxygen generating material is from 1 wt% to 20 wt% of the total composition within the second container, more preferably from 3 wt% to about 15 wt%, most preferably from 6 wt% to 12wt%.
  • the first container preferably comprises a casing comprising a material that is pliable, more preferably the casing is impermeable to air. More preferably the casing material is a laminate, more preferably aluminium. Composition with the First Container
  • the composition within the first composition comprises an oxidative dye.
  • Suitable oxidative dyes for use in the dyeing compositions described herein include, but are not limited to, p-phenylenediamine derivatives, e.g. benzene- 1 ,4-diamine (commonly known as p-phenylenediamine); 2-chloro-benzene- 1 ,4-diamine; N- phenyl-benzene- 1 ,4-diamine; N-(2- ethoxyethyl)benzene- 1 ,4-diamine; 2-[(4- amino-phenyl)-(2-hydroxy-ethyl)-amino]-ethanol (commonly known as N,N-bis(2- hydroxyethyl)-p-phenylenediamine); (2,5-diamino-phenyl)- methanol; l-(2'- Hydroxyethyl)-2,5-diaminobenzene
  • Additional developers may be selected from 7V-(3-furylmethyl)ben/ene-l,4- diamine; N- thiophen-3-ylmethyl-benzene-l,4-diamine; A/-(2-furylraethyl)ben/ene- l,4-diaitune; N-thiophen- 2-ylmethyl-benzene-l,4-diamine: 3-(2,5-diamino-phenyl)- N-ethyl-acrylamide; 2-[3-(3-amino- phenylamino)-propenyl]-benzene-l,4-diamine; 2-[3-(4-amino-phenylannino)-propenyl]-benzene- 1 ,4-diamine; 2-(6-methyl-pyridin- 2-yl)-benzene-l,4-diamine; 2-pyridin-2-yl-benzene-l,4-
  • biphenyl-2,4,4'-triannine 5-(4-amino-phenyl)aminomethyl- benzene- 1 , 3 -diamine hydrochloride; 2- [4- amino-2- (3, 5 -diamino-benzylamino) -phenoxy ] - ethanol hydrochloride; 5-allylaminomethyl-benzene-l,3-diannine hydrochloride; 5-(3-amino- phenyl)aminonnethyl-benzene- 1 ,3-diamine hydrochloride; N-(4-amino-benzyl)- benzene- 1 ,3- diamine hydrochloride; N-benzyl-benzene- 1 ,3-diamine
  • hydrochloride 3-[(3-amino- phenylamino) -methyl] -phenol hydrochloride; N-(2- amino-benzy 1 ) -benzene- 1 , 3 -diamine hydrochloride; N-(4-methoxy-benzyl)- benzene-l,3-diamine hydrochloride; N-furan-2-ylmethyl- benzene- 1 ,3-diamine hydrochloride; 2-[(3-amino-phenylamino)-methyl]-phenol hydrochloride; N- thiophen-2-ylmethyl-benzene- 1 ,3-diamine hydrochloride; N-benzo[l,3]dioxol-5- ylmethyl- benzene- 1 ,3-diamine hydrochloride; N-[4-amino-2-(2-hydroxy-ethyl)-2H- pyrazol-3-yl]-3-(5- amino-2
  • developers include but are not limited to: p-preferred phenylenediamine derivatives such as: 2-methyl-benzene-l,4-diamine; benzene- 1 ,4-diamine; l-(2,5-diamino- phenyl)-ethanol; 2-(2,5-diamino-phenyl)-ethanol; 2- (methoxymethyl)benzene- 1 ,4-diamine; ?- (2-methoxyethyl)benzene- 1 ,4-diamine; 2-[(4-amino-phenyl)-(2-hydroxy-ethyl)-amino]-ethanol; l-(2,5- diaminophenyl)ethane-l,2-diol; l-(2'-hydroxyethyl)-2,5-diaminobenzene; l,3-bis(?- (2- hydroxyethyl)-N-(4-amino
  • Particularly preferred developers for combination with 4, 5-diaminopyrazole are base selected from toluene 2-5 diamine sulphate and para-amino-phenol.
  • the composition in the first container preferably further comprises a coupler.
  • Suitable couplers for use in the dyeing compositions include, but are not limited to: phenols, resorcinols, naphthols, m-aminophenols, m-phenylenediamines, and heterocyclic compounds, and derivatives thereof such as: 2-amino-5-ethyl-phenol; naphthalene- 1 ,7-diol; benzene- 1 ,3-diol; 4-chlorobenzene-l,3-diol; naphthalen-1 - ol; 2-methyl-naphthalen-l-ol; naphthalene- 1 ,5-diol; naphthalene-2,7-diol;
  • benzene- 1 ,4-diol 2-methyl-benzene-l,3-diol; 7- amino-4-hydroxy-naphthalene-2- sulfonic acid; 2-isopropyl-5-methylphenol; 1 ,2,3,4-tetrahydro- naphthalene- 1 ,5- diol; 2-chloro-benzene-l,3-diol; 4-hydroxy-naphthalene-l-sulfonic acid; benzene- 1,2,3-triol; naphthalene-2,3-diol; 5-dichloro-2-methylbenzene-l,3-diol; 4,6- dichlorobenzene- 1 ,3-diol; 2,3-dihydroxy-[l,4]naphthoquinone; and l-Acetoxy-2- methylnaphthalene; m-phenylenediamines such as: 2,4-diamino
  • couplers include but are not limited to: phenol, resorcinol, and naphthol derivatives such as: 2-amino-5-ethyl-phenol; naphthalene- 1 ,7-diol; benzene-l,3-diol; 4-chlorobenzene-l,3-diol; naphthalen-1 -ol; 2-methyl-naphthalen- l-ol; naphthalene- 1 , 5 -diol; naphthalene-2,7-diol; benzene- 1 ,4-diol; 2-methyl - benzene- 1 ,3-diol; and 2-isopropyl-5- methylphenol; 1 ,2,4-trihydroxybenzene; I- acetoxy-2-methylnaphthalene; and mixtures thereof; m-phenylenediamine derivatives such as: benzene- 1 ,
  • Preferred coupler include: 2-methylresorcinol, 2,4-diaminophenoxyethananol, resorcinol, 1 -napthol, 2-methyl-5-hydroxyethylaminophenol, 4-amino-2- hydroxytoluene, meta-aminophenol and 2-amino-4-hydroxyethylaminoanisole sulphate. Particularly preferred is meta amino-phenol, especially when used in combination with a second coupler.
  • the dyeing compositions of the present invention will generally comprise from about 0.001 percent to about 10 percent by weight of the dyeing composition of developer and coupler dyes.
  • dyeing compositions providing low intensity dyeing such as natural blond to light brown hair shades generally comprise from about 0.001 percent to about 5 percent, in some embodiments, from about 0.1 percent to about 2 percent, in certain embodiments, from about 0.2 percent to about 1 percent by weight of dyeing composition of developers and couplers.
  • Darker shades such as browns and black typically comprise from 0.001 percent to about 10 percent by weight, in some embodiments, from about 0.05 percent to about 7 percent by weight, in certain embodiments, from about 1 percent to about 5 percent by weight of the dyeing composition of developers and couplers.
  • Oxidative dyes are generally used in approximately equimolar quantities with respect to coupler compounds, preferably at molar ratio of developer to coupler from 0.95 to 1 .05.
  • the dyeing compositions within the first container may also comprise compatible direct dyes, in an amount sufficient to provide coloring, particularly with regard to intensity. Typically, such an amount will range from about 0.05 percent to about 4 percent, by weight of the dyeing composition.
  • Suitable direct dyes include but are not limited to: Acid Yellow 1 ; Acid Orange 3; Disperse Red 17; Basic Brown 17; Acid Black 52; Acid Black 1 ; Disperse Violet 4; 4-nitro-o-phenylenediamine; 2- nitro-p-phenylenediamine; Picramic Acid; HC Red No. 13; l,4-bis-(2'- hydroxyethyl)-amino-2- nitrobenzene; HC Yellow No. 5; HC Red No. 7; HC Blue No. 2; HC Yellow No. 4; HC Yellow
  • Preferred direct dyes include but are not limited to: Disperse Black 9; HC Yellow 2; HC Yellow 4; HC Yellow 15; 4-nitro-o- phenylenediamine; 2-amino-6-chloro-4-nitrophenol; HC Red 3; Disperse Violet 1 ; HC Blue 2; Disperse Blue 3; Disperse Blue 377; Basic Red 51 ; Basic Orange 31 ; Basic Yellow 87; and mixtures thereof.
  • compositions within the containers may comprise a solvent comprising water or a mixture of water and at least one organic solvent to dissolve the compounds present in the dyeing composition or colorant composition that would not typically be sufficiently soluble in water.
  • Suitable organic solvents for use herein include, but are not limited to: Ci to C 4 lower alkanols (e.g., ethanol, propanol,
  • isopropanol aromatic alcohols (e.g. benzyl alcohol and phenoxyethanol); polyols and polyol ethers (e.g., carbitols, 2-butoxyethanol, propylene glycol, propylene glycol monomethyl ether, diethylene glycol monoethyl ether, monomethyl ether, hexylene glycol, glycerol, ethoxy glycol), and propylene carbonate.
  • organic solvents are typically present in an amount ranging from about 1 percent to about 30 percent, by weight of the dyeing composition or the colorant composition.
  • the solvent comprises water, ethanol, propanol, isopropanol, glycerol, 1 ,2-propylene glycol, hexylene glycol, ethoxy diglycol, or mixtures thereof.
  • compositions may comprise a thickener in an amount sufficient to provide the colorant composition with a viscosity so that it can be readily applied to the hair without unduly dripping off the hair and causing mess.
  • a thickener in an amount sufficient to provide the colorant composition with a viscosity so that it can be readily applied to the hair without unduly dripping off the hair and causing mess.
  • such an amount will be at least about 0.1 percent, in some embodiments, at least about 0.5 percent, in other embodiments, at least about 1 percent, by weight of the colorant composition.
  • salt tolerant thickeners including but not limited to: xanthan, guar, hydroxypropyl guar, scleroglucan, methyl cellulose, ethyl cellulose (available as AQUACOTE (TM)), hydroxyethyl cellulose (NATROSOL (TM)), carboxymethyl cellulose, hydroxypropyl methyl cellulose, microcrystalline cellulose, hydroxybutyl methyl cellulose, hydroxypropyl cellulose (available as KLUCEL (TM)), hydroxyethyl ethyl cellulose, cetyl hydroxyethyl cellulose (available as NATROSOL (TM) Plus 330), N-vinylpyrollidone (available as POVIDONE (TM)), Acrylates/Ceteth-20 Itaconate Copolymer (available as STRUCTURE (TM) 3001 ), hydroxypropyl starch phosphate (available as STRUCTURE (TM) ZEA), polyethoxyl
  • PEG- 150/Decyl/SMDI copolymer available as ACULYN(TM) 44
  • PEG- 150/Stearyl/SMDI copolymer available as ACULYN(TM) 46
  • trihydroxystearin available as THIXCIN(TM)
  • acrylates copolymer e.g. available as ACULYN(TM) 33
  • hydrophobically modified acrylate copolymers e.g.
  • compositions may further comprise a pH modifier and/or buffering agent in an amount that is sufficiently effective to adjust the pH of the colorant composition to fall within a range from about 3 to about 13, in some embodiments, from about 8 to about 12, in certain embodiments, from about 9 to about 1 1 .
  • Suitable pH modifiers and/or buffering agents for use herein include, but are not limited to: ammonia, alkanolamides such as monoethanolamine, diethanolamine, triethanolamine, monopropanolamine, dipropanolamine, tripropanolamine, tripropanolamine, 2-amino-2-nnethyl- 1 -propanol, and 2-amino-2-hydroxymethyl- 1,3,-propandiol and guanidium salts, alkali metal and ammonium hydroxides and carbonates, in some embodiments, sodium hydroxide and ammonium carbonate, and acidulents such as inorganic and inorganic acids, e.g., phosphoric acid, acetic acid, ascorbic acid, citric acid or tartaric acid, hydrochloric acid, and mixtures thereof.
  • inorganic and inorganic acids e.g., phosphoric acid, acetic acid, ascorbic acid, citric acid or tartaric acid, hydrochloric acid,
  • compositions may further comprise additional components, e.g., formulation components, known, conventionally used, or otherwise effective for use in colorant compositions such as carbonate ion sources; peroxymonocarbonate ion sources; anionic, cationic, nonionic, amphoteric or zwitterionic surfactants, or mixtures thereof; anionic, cationic, chelants, nonionic, amphoteric or zwitterionic, amino sugars, antifoams, antioxidants, esters of amino acids or mixtures thereof, buffers; dispersing agents; peroxide stabilizing agents; natural ingredients, e.g. proteins and protein derivatives, and plant extracts; silicones (volatile or nonvolatile, modified or non-modified), film-forming agents, ceramides, preserving agents; and opacifiers.
  • additional components e.g., formulation components, known, conventionally used, or otherwise effective for use in colorant compositions such as carbonate ion sources; peroxymonocarbonate ion sources
  • These compounds may be present in the dyeing compositions and colorant compositions at a concentration of from about 0.01 percent to about 10 percent by weight of the total colouring composition, more preferably from about 0.1 percent to about 7 percent by weight.
  • Figure 1 represents a view relating to cross section of an a embodiment of the second container of the invention.
  • the container 1 has a bottom C and substantially parallel the bottom to an opening A.
  • the sides B of the container are tapered towards the opening to form neck D, the formation of the neck leads to a lip E within the container.
  • the base of the container is domed F.
  • the base of container has an external diameter Y mm, the sides of the container have a height X mm and the opening of the container has an internal diameter Z mm.

Landscapes

  • Cosmetics (AREA)
EP14701170.4A 2013-01-31 2014-01-20 Haarfärbekit Ceased EP2950678A1 (de)

Priority Applications (1)

Application Number Priority Date Filing Date Title
EP14701170.4A EP2950678A1 (de) 2013-01-31 2014-01-20 Haarfärbekit

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
EP13153385 2013-01-31
EP14701170.4A EP2950678A1 (de) 2013-01-31 2014-01-20 Haarfärbekit
PCT/EP2014/051024 WO2014118027A1 (en) 2013-01-31 2014-01-20 Hair colouring kit

Publications (1)

Publication Number Publication Date
EP2950678A1 true EP2950678A1 (de) 2015-12-09

Family

ID=47628035

Family Applications (1)

Application Number Title Priority Date Filing Date
EP14701170.4A Ceased EP2950678A1 (de) 2013-01-31 2014-01-20 Haarfärbekit

Country Status (8)

Country Link
US (1) US20150351517A1 (de)
EP (1) EP2950678A1 (de)
JP (1) JP2016515998A (de)
CN (1) CN104955358A (de)
AR (1) AR094611A1 (de)
BR (1) BR112015017512A2 (de)
TW (1) TW201446180A (de)
WO (1) WO2014118027A1 (de)

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20070017542A1 (en) * 2005-06-06 2007-01-25 Techpack International Dispenser for a product in powder form
FR2967143A1 (fr) * 2010-11-10 2012-05-11 Oreal Ensemble de conditionnement de produits a melanger extemporanement et procede pour realiser un tel ensemble

Family Cites Families (18)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1617825C3 (de) * 1966-03-03 1974-11-28 Hans Schwarzkopf Gmbh, 2000 Hamburg Vorrichtung zum Mischen und Versprühen einer aus wenigstens zwei flüssigen, pulverförmigen oder pastenförmigen Bestandteilen und einem Treibgas bestehenden Mischung
US3871541A (en) * 1973-02-26 1975-03-18 Continental Can Co Bottom structure for plastic containers
JPS5017178U (de) * 1973-06-11 1975-02-24
US4834256A (en) * 1987-07-31 1989-05-30 Pac International, Inc. Can with domed bottom structure
US5636761A (en) * 1995-10-16 1997-06-10 Dispensing Containers Corporation Deformation resistant aerosol container cover
FR2761962B1 (fr) * 1997-04-14 1999-06-04 Oreal Barquette thermoplastique pour le melange extemporane d'au moins deux produits
US5972043A (en) 1998-03-17 1999-10-26 Galvan; Tim Methods for mixing and applying hair coloring compounds, and hair coloring devices and kits which comprise a brush and an enclosed mixing bowl
US20040188469A1 (en) * 2003-03-28 2004-09-30 Lambrakis William G. Hair coloring application system
JP2004313403A (ja) * 2003-04-15 2004-11-11 Hoyu Co Ltd 染毛用カップ及びプレート
US7407055B2 (en) * 2003-09-25 2008-08-05 Rodriguez Deborah T Hair roots coloring kit
DE202004019474U1 (de) 2004-12-15 2005-12-29 Henkel Kgaa Schale
HRP20110507T1 (hr) * 2007-04-27 2011-08-31 Kao Corporation Postupak bojanja ili izbjeljivanja kose
EP2564829A1 (de) * 2007-04-27 2013-03-06 Kao Corporation Zweiteilige Haarfärbe- oder -bleichzusammensetzung
TWI407973B (zh) * 2008-05-30 2013-09-11 Kao Corp 二劑式泡狀染毛劑
JP2011184428A (ja) 2010-02-10 2011-09-22 Kao Corp 染色又は脱色キット
JP5829461B2 (ja) * 2010-08-30 2015-12-09 花王株式会社 毛髪の染毛又は脱色方法、及び染毛用又は脱色用キット
KR20120002659U (ko) * 2010-10-11 2012-04-19 조규만 통합 용기 염색제
TW201247137A (en) * 2011-05-20 2012-12-01 Wu Chen Wen Container for hair dyeing

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20070017542A1 (en) * 2005-06-06 2007-01-25 Techpack International Dispenser for a product in powder form
FR2967143A1 (fr) * 2010-11-10 2012-05-11 Oreal Ensemble de conditionnement de produits a melanger extemporanement et procede pour realiser un tel ensemble

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See also references of WO2014118027A1 *

Also Published As

Publication number Publication date
US20150351517A1 (en) 2015-12-10
CN104955358A (zh) 2015-09-30
JP2016515998A (ja) 2016-06-02
BR112015017512A2 (pt) 2017-07-11
TW201446180A (zh) 2014-12-16
WO2014118027A1 (en) 2014-08-07
AR094611A1 (es) 2015-08-12

Similar Documents

Publication Publication Date Title
US7985266B2 (en) Keratin dyeing compositions comprising a radical scavenger and a chelant and use thereof
US7988740B2 (en) Keratin dyeing compositions comprising a radical scavenger and use thereof
EP1720615B1 (de) Kosmetische haarfärbezusammensetzungen und ihre verwendung
US7331997B2 (en) Keratin dyeing compounds, keratin dyeing compositions containing them, and use thereof
US20060156485A1 (en) Keratin dyeing compounds, keratin dyeing compositions containing them, and use thereof
JP5795597B2 (ja) 増粘毛髪染色剤及び脱色組成物
EP1646606A1 (de) 2-(amino- oder substituiertes amino)-5-(substituiertes oxymethyl)phenolverbindungen, färbzusammensetzungen, die diese enthalten, und deren anwendungen
US7399317B2 (en) Keratin dyeing compounds, keratin dyeing compositions containing them, and use thereof
EP2274286B1 (de) Keratinfärbungsverbindungen, keratinfärbungszusammensetzungen damit und verwendung davon
US7371264B2 (en) Keratin dyeing compounds, keratin dyeing compositions containing them, and use thereof
EP1744720B1 (de) Keratin-färbemittel enthaltend bizyklische 5-5-heteroaromatische färbekomponenten
US20150351517A1 (en) Hair colouring kit
WO2013107524A1 (en) Hair colouring composition
US20060162099A1 (en) Keratin dyeing compounds, keratin dyeing compositions containing them, and use thereof
US7341606B2 (en) Keratin dyeing compounds, keratin dyeing compositions containing them, and use thereof
US20080092306A1 (en) Keratin Dyeing Compounds, Keratin Dyeing Compositions Containing Them, And Use Thereof

Legal Events

Date Code Title Description
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

17P Request for examination filed

Effective date: 20150703

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

AX Request for extension of the european patent

Extension state: BA ME

17Q First examination report despatched

Effective date: 20160307

DAX Request for extension of the european patent (deleted)
STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: EXAMINATION IS IN PROGRESS

REG Reference to a national code

Ref country code: DE

Ref legal event code: R003

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

Free format text: STATUS: THE APPLICATION HAS BEEN REFUSED

18R Application refused

Effective date: 20190207