WO2005080507A1 - Aufhellendes färbemittel mit indolylthiazoliumazofarbstoffen - Google Patents
Aufhellendes färbemittel mit indolylthiazoliumazofarbstoffen Download PDFInfo
- Publication number
- WO2005080507A1 WO2005080507A1 PCT/EP2004/013706 EP2004013706W WO2005080507A1 WO 2005080507 A1 WO2005080507 A1 WO 2005080507A1 EP 2004013706 W EP2004013706 W EP 2004013706W WO 2005080507 A1 WO2005080507 A1 WO 2005080507A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- azo
- indol
- methyl
- thiazolium
- dimethyl
- Prior art date
Links
- 0 C*[n+]1c(N=Nc2c(C)[n](*)c3c(*)c(*)c(*)c(*)c23)[s]c(C)c1C Chemical compound C*[n+]1c(N=Nc2c(C)[n](*)c3c(*)c(*)c(*)c(*)c23)[s]c(C)c1C 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B44/00—Azo dyes containing onium groups
- C09B44/10—Azo dyes containing onium groups containing cyclammonium groups attached to an azo group by a carbon atom of the ring system
- C09B44/20—Thiazoles or hydrogenated thiazoles
Definitions
- the present invention relates to agents for the simultaneous dyeing and lightening of keratin fibers, such as wool, silk or hair and in particular human hair, which contain at least one indolylthiazolium azo dye.
- Two dyeing processes are generally used for the color-changing treatment of keratin fibers.
- the coloring is produced with so-called oxidative or permanent coloring agents, using a mixture of different developer substances and coupler substances and an oxidizing agent.
- so-called direct (non-oxidative) dyes can be added in this process to round off the coloring result or to produce special color effects.
- the second method uses only direct dyes that are applied to the fibers in a suitable carrier. This process is easy to use, extremely gentle and is characterized by low damage to the keratin fiber. A large number of requirements are imposed on the direct dyes used here.
- the present invention therefore relates to an agent for simultaneously lightening and coloring keratin fibers, in particular hair, which is characterized in that it contains (a) an oxidizing agent and (b) at least one indolylthiazolium azo dye of the formula (I), and (c) has a basic pH,
- R1 is a saturated or unsaturated (C C ⁇ 2 ) alkyl group, one with a
- R2 and R3 can be the same or different and independently of one another hydrogen, a halogen atom (F, Cl, Br, J), a saturated or unsaturated (CrC 2 ) alkyl group, a (dC- ⁇ 2 ) alkoxy group, a nitro group, an amino group, a (CrC ⁇ 2 ) alkyla
- R4 is a saturated or unsaturated (C ⁇ -C ⁇ 2 ) alkyl group, a (C- ⁇ -C ⁇ 2 ) alkyl group substituted by a halogen atom (F, Cl, Br, J), a hydroxy (C C ⁇ 2 ) alkyl group, a (CrC 6 ) alkoxy (CrC ⁇ 2 ) alkyl group, an amino (C- ⁇ -C ⁇ 2 ) alkyl group, a (C- ⁇ -C 6 ) alkylamino- (C ⁇ -C- ⁇ 2 ) alkyl - Group, a di (-C 6 ) alkylamino (CrC ⁇ 2 ) alkyl group, a cyano (C ⁇ -C 2 ) alkyl group, a substituted or unsubstituted phenyl group, a substituted or unsubstituted benzyl group or a substituted or unsubstituted Represents hetero-aryl group; R5 is
- R6, R7, R8 and R9 may be the same or different and, independently of one another, hydrogen, a halogen atom (F, Cl, Br, J), a saturated or unsaturated (C 1 -C 2 ) alkyl group, a hydroxy group, a (1 CrC ⁇ 2 ) - Alkoxy group, a nitro group, an amino group, a or represent a di (CrC 12 ) alkylamino group; and A ' is an anion of an organic or inorganic acid.
- a halogen atom F, Cl, Br, J
- C 1 -C 2 alkyl group saturated or unsaturated alkyl group
- a hydroxy group a (1 CrC ⁇ 2 ) - Alkoxy group
- a nitro group an amino group
- a ' is an anion of an organic or inorganic acid.
- Preferred compounds of the formula (I) are those in which R1 is a saturated or unsaturated (-C 1 -C 2 ) alkyl group and R4 is a saturated or unsaturated (CrC 1 2 ) alkyl group or a substituted or unsubstituted phenyl group is. Particularly preferred are compounds of formula (I) in which R1 is a saturated (C 1 -C 2 ) alkyl group and R4 is a saturated (C 1 -C 2 ) alkyl group or an unsubstituted phenyl group.
- a " is preferably the same as chloride, bromide, iodide, hydrogen sulfate, sulfate, toluenesulfonate, benzenesulfonate, monomethyl sulfate, hexafluorophosphate, hexafluoroantimonate, tetrafluoroborate, tetraphenylborate, formate, acetate or propionate, with the chloride ion, the bromide sulfate ion and the mono- especially being preferred.
- Particularly preferred compounds of the formula (I) are 3-methyl-2 - [(1-methyl-2-phenyl-1H-indol-3-yl) azo] thiazolium chloride, 3-methyl-2 - [(1 - methyl-2-phenyl-1 H-indol-3-yl) azo] thiazolium bromide, 3-methyl-2 - [(1 - methyl-2-phenyl-1 H-indol-3-yl) azo] -thiazolium monomethyl sulfate, 3,4-dimethyl-2 - [(1-methyl-2-phenyl-1H-indol-3-yl) azo] thiazolium chloride, 3,4-dimethyl-2 - [(1- methyl-2-phenyl-1H-indol-3-yl) azo] thiazolium bromide, 3,4-dimethyl-2 - [(1-methyl-2-phenyl-1H-indol-3-yl)
- the compounds of the formula (I) are preferably present in the colorant according to the invention in an amount of 0.01 to 10 percent by weight, in particular 0.1 to 8 percent by weight.
- the total content of dyes of the formula (I) and direct-coloring dyes in the colorant according to the invention is about 0.01 to 15 percent by weight, in particular about 0.1 to 12 percent by weight.
- oxidation dye precursors such as, for example, o, p, m-phenylenediamines, o, p, m-aminophenols, diphenols or 4,5-diaminopyrazoles, can also be added to the colorant according to the invention.
- additional developer substances and coupler substances can each be present in the colorant in a total amount of about 0.01 to 20 percent by weight, preferably about 0.1 to 10 percent by weight and in particular 0.1 to 5 percent by weight.
- the preparation form of the colorant according to the invention can be, for example, a solution, in particular an aqueous or aqueous-alcoholic solution, a cream, a gel, a surfactant-containing gum. ing solution (shampoo, aerosol), an emulsion or another water-based carrier suitable for use on the hair. It is also possible for the colorant according to the invention to be in the form of pellets, granules or powders, which are dissolved in an aqueous preparation, for example in water or an aqueous oxidizing agent preparation, before use.
- the composition of these agents is a mixture of the dye component with the additives customary for such preparations.
- Usual additives in solutions, creams, emulsions or gels are, for example, solvents such as water, lower aliphatic monohydric or polyhydric alcohols, their esters and ethers, for example alkanols, in particular with 1 to 4C atoms, for example ethanol, propanol or isopropanol, butanol, isobutanol , dihydric and trihydric alcohols, in particular those having 2 to 6 carbon atoms, for example ethylene glycol, propylene glycol, 1, 3-propanediol, 1, 4-butanediol, 1, 5-pentanediol, 1, 6-hexanediol, 1, 2 , 6-hexanthol, glycerin, diethylene glycol, dipropylene glycol, polyalkylene glycols, such as triethylene glycol, polyethylene glycol, tripropylene glycol, polypropylene glycol, lower alkyl ethers of polyhydric alcohols,
- wetting agents or emulsifiers from the classes of the anionic, cationic, amphoteric, nonionic or zwitterionic surface-active substances such as fatty alcohol sulfates, oxyethylated fatty alcohol sulfates, alkyl sulfonates, alkylbenzenesulfonates, ⁇ -olefin sulfonates, alkyltrimethylammonium alkali metal salts, oxyethylated fatty alcohols, oxyethylated oxychloride salts, oxyethyl salts, oxyethyl salts, and alkyltrimethylammonium alkali metal salts, and can be used in the colorant according to the invention
- constituents mentioned are used in the amounts customary for such purposes, for example the wetting agents and emulsifiers in con- concentrations of about 0.1 to 30 percent by weight, the thickeners in an amount of about 0.1 to 30 percent by weight and the care substances in a concentration of about 0.1 to 5 percent by weight.
- the ready-to-use colorant according to the invention is produced immediately before use by mixing the colorant composition comprising the dyes with an oxidizing agent.
- the main oxidizing agents that can be used are hydrogen peroxide or its addition compounds with urea, melamine, sodium borate or sodium carbonate in the form of a 1 to 12 percent, preferably a 3 to 9 percent, aqueous solution.
- the weight ratio between the colorant and oxidizing agent is preferably about 5: 1 to 1: 3, in particular 1: 1 to 1: 2. Larger amounts of oxidizing agent are used above all at higher concentrations of oxidative dye precursors in the coloring agent, or if at the same time a stronger bleaching of the keratin fiber (in particular the hair) is intended.
- persulfates such as, for example, ammonium persulfate, potassium persulfate or sodium persulfate and mixtures thereof, is possible, provided the dyes of the formula (I) are stable to persulfates ,
- the pH value of the ready-to-use colorant according to the invention is adjusted when the color carrier mass is mixed with the oxidizing agent to a pH value which is determined by the pH values of the color carrier mass of the oxidizing agent and by the mixing ratio.
- the ready-to-use agent has a basic pH of greater than 7, preferably a pH of 8 to 11.
- the basic attitude is preferably carried out with ammonia, but also organic amines, for example 2-amino-2-methyl-1-propanol, tris (hydroxymethyl) amino-methane, monoethanolamine and triethanolamine, or mixtures of organic amines and ammonia and inorganic bases such as sodium hydroxide, potassium hydroxide, sodium carbonate, sodium hydrogen carbonate, potassium carbonate, potassium hydrogen carbonate, sodium phosphate, borax (Na 2 BO 7 x 10H 2 O), disodium hydrogen phosphate can be used. If the pH values are too high, correction can be made with inorganic or organic acids, for example phosphoric acid, acetic acid, lactic acid, ascorbic acid, citric acid or tartaric acid.
- organic amines for example 2-amino-2-methyl-1-propanol, tris (hydroxymethyl) amino-methane, monoethanolamine and triethanolamine, or mixtures of organic amines and ammonia and inorganic bases
- an amount sufficient for the dyeing treatment generally about 30 to 120 grams, of this mixture is applied to the keratin fiber and the mixture is left at about 15 to 50 ° C., preferably 30 to 40 ° C., for about 1 to 60 minutes, act on the keratin fiber for preferably 5 to 30 minutes, then rinse the keratin fiber with water and dry it. If necessary, this rinse is washed with a shampoo and possibly rinsed with a weak organic acid, such as citric acid or tartaric acid. The keratin fiber is then dried.
- aqueous component used for the dilution can contain the usual additives for solutions, creams, emulsions mentioned above. or gels.
- This process enables dyeings to be matched to the hair texture, which are characterized by a hair-friendly balance between the roots and the tips, which is not possible when using conventional oxidative hair dyes, since an oxidizing agent is always required to couple the dye precursors.
- the colorant according to the invention enables dyeings which are distinguished by their particular color intensity and luminosity, a good color balance between damaged and undamaged hair (for example between the ends of the hair and hair regrowth) and by particularly good lightfastness and sweat resistance.
- dyes of the formula (I) are known per se. They can be produced in analogy to known production processes, for example via azo coupling of 2-aminothiazole derivatives with indole derivatives, and subsequent quaternization.
- the above coloring solution 5 g are mixed with 5 g of a 9% hydrogen peroxide solution.
- the coloring solution is adjusted to the desired pH by adding ammonia.
- the ready-to-use hair dye obtained is applied to dark blonde hair and is evenly distributed with a brush. After an exposure time of 30 minutes at 40 ° C, the hair is rinsed with lukewarm water, washed with a shampoo, rinsed with lukewarm water and then dried.
- A) Invention 5 g of the above coloring solution are mixed with 5 g of a 9% hydrogen peroxide solution.
- the coloring solution is adjusted to the desired pH by adding ammonia.
- the ready-to-use hair dye obtained is applied to dry dark blonde natural hair and is evenly distributed with a brush. After an exposure time of 30 minutes at 40 ° C, the hair is rinsed with lukewarm water, using a shampoo washed, rinsed with lukewarm water and then dried.
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Cosmetics (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Coloring (AREA)
Abstract
Description
Claims
Priority Applications (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP04803448A EP1730239B1 (de) | 2004-02-21 | 2004-12-02 | Aufhellendes färbemittel mit indolylthiazoliumazofarbstoffen |
DE502004003735T DE502004003735D1 (de) | 2004-02-21 | 2004-12-02 | Aufhellendes färbemittel mit indolylthiazoliumazofarbstoffen |
US10/588,934 US7431741B2 (en) | 2004-02-21 | 2004-12-02 | Brightening colorant with indolythiazolium dyes |
JP2006553456A JP4548797B2 (ja) | 2004-02-21 | 2004-12-02 | インドリルチアゾリウムアゾ染料を有する明色化染色剤 |
BRPI0418559-5A BRPI0418559A (pt) | 2004-02-21 | 2004-12-02 | agente de tingimento clareador com azocorantes de indoliltiazólio |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE102004008606A DE102004008606A1 (de) | 2004-02-21 | 2004-02-21 | Aufhellendes Färbemittel mit Indolylthiazoliumazofarbstoffen |
DE102004008606.0 | 2004-02-21 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2005080507A1 true WO2005080507A1 (de) | 2005-09-01 |
Family
ID=34832914
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/EP2004/013706 WO2005080507A1 (de) | 2004-02-21 | 2004-12-02 | Aufhellendes färbemittel mit indolylthiazoliumazofarbstoffen |
Country Status (8)
Country | Link |
---|---|
US (1) | US7431741B2 (de) |
EP (1) | EP1730239B1 (de) |
JP (1) | JP4548797B2 (de) |
AT (1) | ATE361344T1 (de) |
BR (1) | BRPI0418559A (de) |
DE (2) | DE102004008606A1 (de) |
ES (1) | ES2286703T3 (de) |
WO (1) | WO2005080507A1 (de) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2006013036A1 (de) * | 2004-07-28 | 2006-02-09 | Henkel Kommanditgesellschaft Auf Aktien | Kationische azoverbindungen als direktziehende farbstoffe zur färbung keratinischer fasern |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE102004008607A1 (de) * | 2004-02-21 | 2005-09-08 | Wella Ag | Indolylthiazoliumazofarbstoffe enthaltende Färbemittel für Keratinfasern |
US8655744B2 (en) * | 2010-06-21 | 2014-02-18 | Esalon.Com, Llc | Custom hair coloring identification |
US10532335B1 (en) | 2019-03-04 | 2020-01-14 | Esalon.Com, Llc | Hair colorant dispensing system |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB860584A (en) * | 1957-10-24 | 1961-02-08 | Basf Ag | Diazacyanine dyestuff cations |
BE770437A (en) * | 1970-07-24 | 1971-12-01 | Sumitomo Chemical Co | Blue-red cationic dyes - for poly-acrylonitrile, acid - modified polyesters and polyamides |
GB1348665A (en) * | 1970-06-12 | 1974-03-20 | Sumitomo Chemical Co | Cationic dyes |
GB1550306A (en) * | 1976-04-14 | 1979-08-08 | Bayer Ag | Preparation of concentrated solutions of cationic thiazole dyestuffs |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
ES392502A1 (es) * | 1970-06-12 | 1974-07-01 | Sumitomo Chemical Co | Procedimiento de preparacion de compuestos cationicos y me-todo de tenido. |
JPS4817726B1 (de) * | 1970-12-17 | 1973-05-31 | ||
DE3618752A1 (de) * | 1986-06-04 | 1987-12-10 | Bayer Ag | 4,6-dinitrobenzthiazolonhydrazone(2) |
FR2829926B1 (fr) * | 2001-09-26 | 2004-10-01 | Oreal | Composition pour la teinture des fibres keratiniques comprenant un colorant diazoique dicationique particulier |
-
2004
- 2004-02-21 DE DE102004008606A patent/DE102004008606A1/de not_active Withdrawn
- 2004-12-02 EP EP04803448A patent/EP1730239B1/de not_active Not-in-force
- 2004-12-02 JP JP2006553456A patent/JP4548797B2/ja not_active Expired - Fee Related
- 2004-12-02 DE DE502004003735T patent/DE502004003735D1/de active Active
- 2004-12-02 AT AT04803448T patent/ATE361344T1/de not_active IP Right Cessation
- 2004-12-02 BR BRPI0418559-5A patent/BRPI0418559A/pt not_active IP Right Cessation
- 2004-12-02 US US10/588,934 patent/US7431741B2/en not_active Expired - Fee Related
- 2004-12-02 WO PCT/EP2004/013706 patent/WO2005080507A1/de active IP Right Grant
- 2004-12-02 ES ES04803448T patent/ES2286703T3/es active Active
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB860584A (en) * | 1957-10-24 | 1961-02-08 | Basf Ag | Diazacyanine dyestuff cations |
GB1348665A (en) * | 1970-06-12 | 1974-03-20 | Sumitomo Chemical Co | Cationic dyes |
BE770437A (en) * | 1970-07-24 | 1971-12-01 | Sumitomo Chemical Co | Blue-red cationic dyes - for poly-acrylonitrile, acid - modified polyesters and polyamides |
GB1550306A (en) * | 1976-04-14 | 1979-08-08 | Bayer Ag | Preparation of concentrated solutions of cationic thiazole dyestuffs |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2006013036A1 (de) * | 2004-07-28 | 2006-02-09 | Henkel Kommanditgesellschaft Auf Aktien | Kationische azoverbindungen als direktziehende farbstoffe zur färbung keratinischer fasern |
Also Published As
Publication number | Publication date |
---|---|
DE502004003735D1 (de) | 2007-06-14 |
JP4548797B2 (ja) | 2010-09-22 |
BRPI0418559A (pt) | 2007-06-19 |
EP1730239A1 (de) | 2006-12-13 |
DE102004008606A1 (de) | 2005-09-08 |
US7431741B2 (en) | 2008-10-07 |
US20070180631A1 (en) | 2007-08-09 |
JP2007523103A (ja) | 2007-08-16 |
ES2286703T3 (es) | 2007-12-01 |
ATE361344T1 (de) | 2007-05-15 |
EP1730239B1 (de) | 2007-05-02 |
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