RU2009104071A - HAIR COLOR - Google Patents
HAIR COLOR Download PDFInfo
- Publication number
- RU2009104071A RU2009104071A RU2009104071/15A RU2009104071A RU2009104071A RU 2009104071 A RU2009104071 A RU 2009104071A RU 2009104071/15 A RU2009104071/15 A RU 2009104071/15A RU 2009104071 A RU2009104071 A RU 2009104071A RU 2009104071 A RU2009104071 A RU 2009104071A
- Authority
- RU
- Russia
- Prior art keywords
- carbon atoms
- group
- formula
- tool according
- alkyl group
- Prior art date
Links
- 230000037308 hair color Effects 0.000 title 1
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract 32
- 150000001875 compounds Chemical class 0.000 claims abstract 15
- 125000000217 alkyl group Chemical group 0.000 claims abstract 13
- 125000002768 hydroxyalkyl group Chemical group 0.000 claims abstract 13
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract 10
- 125000003342 alkenyl group Chemical group 0.000 claims abstract 7
- 150000001768 cations Chemical class 0.000 claims abstract 6
- 239000000975 dye Substances 0.000 claims abstract 6
- 239000007858 starting material Substances 0.000 claims abstract 6
- 238000004043 dyeing Methods 0.000 claims abstract 4
- 239000000835 fiber Substances 0.000 claims abstract 4
- 102000011782 Keratins Human genes 0.000 claims abstract 3
- 108010076876 Keratins Proteins 0.000 claims abstract 3
- 239000006103 coloring component Substances 0.000 claims abstract 2
- 239000000982 direct dye Substances 0.000 claims abstract 2
- 230000001590 oxidative effect Effects 0.000 claims abstract 2
- -1 genicosanil Chemical group 0.000 claims 7
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 claims 6
- 229910021529 ammonia Inorganic materials 0.000 claims 3
- FSYKKLYZXJSNPZ-UHFFFAOYSA-N sarcosine Chemical compound C[NH2+]CC([O-])=O FSYKKLYZXJSNPZ-UHFFFAOYSA-N 0.000 claims 3
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 claims 2
- SUZRRICLUFMAQD-UHFFFAOYSA-N N-Methyltaurine Chemical compound CNCCS(O)(=O)=O SUZRRICLUFMAQD-UHFFFAOYSA-N 0.000 claims 2
- 239000013543 active substance Substances 0.000 claims 2
- 239000003795 chemical substances by application Substances 0.000 claims 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 2
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 2
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 2
- 150000003839 salts Chemical class 0.000 claims 2
- DABQDIXIAXPQFG-UHFFFAOYSA-N 2-[dodecanoyl(methyl)amino]ethanesulfonic acid Chemical compound CCCCCCCCCCCC(=O)N(C)CCS(O)(=O)=O DABQDIXIAXPQFG-UHFFFAOYSA-N 0.000 claims 1
- LFJJOPDNPVFCNZ-UHFFFAOYSA-N 2-[hexadecanoyl(methyl)amino]acetic acid Chemical compound CCCCCCCCCCCCCCCC(=O)N(C)CC(O)=O LFJJOPDNPVFCNZ-UHFFFAOYSA-N 0.000 claims 1
- VGVRWTPKKMTCFK-UHFFFAOYSA-N 2-[hexadecanoyl(methyl)amino]ethanesulfonic acid Chemical compound CCCCCCCCCCCCCCCC(=O)N(C)CCS(O)(=O)=O VGVRWTPKKMTCFK-UHFFFAOYSA-N 0.000 claims 1
- LTQRFSDXNWHXKQ-UHFFFAOYSA-N 2-[methyl(octadecanoyl)amino]ethanesulfonic acid Chemical compound CCCCCCCCCCCCCCCCCC(=O)N(C)CCS(O)(=O)=O LTQRFSDXNWHXKQ-UHFFFAOYSA-N 0.000 claims 1
- NGOZDSMNMIRDFP-UHFFFAOYSA-N 2-[methyl(tetradecanoyl)amino]acetic acid Chemical compound CCCCCCCCCCCCCC(=O)N(C)CC(O)=O NGOZDSMNMIRDFP-UHFFFAOYSA-N 0.000 claims 1
- FAZHDESNRICLLX-UHFFFAOYSA-N 2-[methyl(tetradecanoyl)amino]ethanesulfonic acid Chemical compound CCCCCCCCCCCCCC(=O)N(C)CCS(O)(=O)=O FAZHDESNRICLLX-UHFFFAOYSA-N 0.000 claims 1
- BMGPYWJNOIMZNC-KHPPLWFESA-N 2-[methyl-[(z)-octadec-9-enyl]amino]acetic acid Chemical compound CCCCCCCC\C=C/CCCCCCCCN(C)CC(O)=O BMGPYWJNOIMZNC-KHPPLWFESA-N 0.000 claims 1
- JACPTQMMZGZAOL-KHPPLWFESA-N 2-[methyl-[(z)-octadec-9-enyl]amino]ethanesulfonic acid Chemical compound CCCCCCCC\C=C/CCCCCCCCN(C)CCS(O)(=O)=O JACPTQMMZGZAOL-KHPPLWFESA-N 0.000 claims 1
- YDNKGFDKKRUKPY-JHOUSYSJSA-N C16 ceramide Natural products CCCCCCCCCCCCCCCC(=O)N[C@@H](CO)[C@H](O)C=CCCCCCCCCCCCCC YDNKGFDKKRUKPY-JHOUSYSJSA-N 0.000 claims 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 1
- BACYUWVYYTXETD-UHFFFAOYSA-N N-Lauroylsarcosine Chemical compound CCCCCCCCCCCC(=O)N(C)CC(O)=O BACYUWVYYTXETD-UHFFFAOYSA-N 0.000 claims 1
- CRJGESKKUOMBCT-VQTJNVASSA-N N-acetylsphinganine Chemical compound CCCCCCCCCCCCCCC[C@@H](O)[C@H](CO)NC(C)=O CRJGESKKUOMBCT-VQTJNVASSA-N 0.000 claims 1
- 108010009736 Protein Hydrolysates Proteins 0.000 claims 1
- 208000003251 Pruritus Diseases 0.000 claims 1
- 108010077895 Sarcosine Proteins 0.000 claims 1
- 206010040880 Skin irritation Diseases 0.000 claims 1
- 125000004429 atom Chemical group 0.000 claims 1
- 229910052799 carbon Inorganic materials 0.000 claims 1
- 229940106189 ceramide Drugs 0.000 claims 1
- ZVEQCJWYRWKARO-UHFFFAOYSA-N ceramide Natural products CCCCCCCCCCCCCCC(O)C(=O)NC(CO)C(O)C=CCCC=C(C)CCCCCCCCC ZVEQCJWYRWKARO-UHFFFAOYSA-N 0.000 claims 1
- 230000002708 enhancing effect Effects 0.000 claims 1
- 229910052739 hydrogen Inorganic materials 0.000 claims 1
- 239000001257 hydrogen Substances 0.000 claims 1
- 230000007803 itching Effects 0.000 claims 1
- 125000002960 margaryl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims 1
- 230000000116 mitigating effect Effects 0.000 claims 1
- VVGIYYKRAMHVLU-UHFFFAOYSA-N newbouldiamide Natural products CCCCCCCCCCCCCCCCCCCC(O)C(O)C(O)C(CO)NC(=O)CCCCCCCCCCCCCCCCC VVGIYYKRAMHVLU-UHFFFAOYSA-N 0.000 claims 1
- 125000001196 nonadecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims 1
- 125000001400 nonyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims 1
- 125000002958 pentadecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims 1
- 150000008442 polyphenolic compounds Chemical class 0.000 claims 1
- 235000013824 polyphenols Nutrition 0.000 claims 1
- 229920001296 polysiloxane Polymers 0.000 claims 1
- 238000003672 processing method Methods 0.000 claims 1
- 239000003531 protein hydrolysate Substances 0.000 claims 1
- 229940043230 sarcosine Drugs 0.000 claims 1
- 108700004121 sarkosyl Proteins 0.000 claims 1
- 210000004761 scalp Anatomy 0.000 claims 1
- 230000035807 sensation Effects 0.000 claims 1
- 230000036556 skin irritation Effects 0.000 claims 1
- 231100000475 skin irritation Toxicity 0.000 claims 1
- 125000002889 tridecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims 1
- 125000002948 undecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims 1
- 238000005406 washing Methods 0.000 claims 1
Classifications
-
- 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
- A61Q5/065—Preparations for temporary colouring the hair, e.g. direct dyes
-
- 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
- A61K8/44—Aminocarboxylic acids or derivatives thereof, e.g. aminocarboxylic acids containing sulfur; Salts; Esters or N-acylated derivatives thereof
-
- 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
- A61K8/46—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing sulfur
- A61K8/466—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing sulfur containing sulfonic acid derivatives; Salts
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Birds (AREA)
- Epidemiology (AREA)
- Cosmetics (AREA)
Abstract
1. Средство для окрашивания содержащих кератин волокон, прежде всего человеческих волос, основа которого содержит по меньшей мере один окрашивающий компонент и дополнительно по меньшей мере одно соединение, выбранное из группы, включающей ! (а) производные N-ацилсаркозина формулы (I) ! ! в которой R1 означает алкильную группу с 7-30 атомами углерода, алкенильную группу с 7-30 атомами углерода или гидроксиалкильную группу с 7-30 атомами углерода, ! R2 означает алкильную группу с 1-4 атомами углерода или гидроксиалкильную группу с 1-4 атомами углерода и ! М означает атом водорода или эквивалент одновалентного или многовалентного катиона, и ! b) производные N-ацилтаурина формулы (II) ! !в которой R3 означает атом водорода, алкильную группу с 1-4 атомами углерода или гидроксиалкильную группу с 1-4 атомами углерода, ! R4 означает алкильную группу с 7-30 атомами углерода, алкенильную группу с 7-30 атомами углерода или гидроксиалкильную группу с 7-30 атомами углерода и ! М' означает атом водорода или эквивалент одновалентного или многовалентного катиона. ! 2. Средство по п.1, отличающееся тем, что окрашивающий компонент предпочтительно выбирают из группы, включающей ! (1) по меньшей мере один исходный продукт для окислительного красителя типа проявляющих компонентов и при необходимости дополнительно по меньшей мере один цветообразующий компонент, и/или ! (2) исходные продукты для оксокрасителей, и/или ! (3) по меньшей мере один прямой краситель, и/или ! (4) по меньшей мере одно исходное соединение для красителей, аналогичных природным. ! 3. Средство по п.1, отличающееся тем, что R1 в соединениях формулы (I) и R4 в соединениях формулы (II) независимо друг 1. Means for dyeing keratin-containing fibers, especially human hair, the base of which contains at least one dyeing component and additionally at least one compound selected from the group consisting of! (a) N-acylsarcosine derivatives of formula (I)! ! in which R1 means an alkyl group with 7-30 carbon atoms, an alkenyl group with 7-30 carbon atoms or a hydroxyalkyl group with 7-30 carbon atoms,! R2 means an alkyl group with 1-4 carbon atoms or a hydroxyalkyl group with 1-4 carbon atoms and! M means a hydrogen atom or the equivalent of a monovalent or multivalent cation, and! b) derivatives of N-acyltaurin of the formula (II)! ! in which R3 is a hydrogen atom, an alkyl group with 1-4 carbon atoms or a hydroxyalkyl group with 1-4 carbon atoms,! R4 means an alkyl group with 7-30 carbon atoms, an alkenyl group with 7-30 carbon atoms or a hydroxyalkyl group with 7-30 carbon atoms and! M 'means a hydrogen atom or the equivalent of a monovalent or multivalent cation. ! 2. The tool according to claim 1, characterized in that the coloring component is preferably selected from the group including! (1) at least one starting material for an oxidative dye of the type of developing components, and optionally at least one color-forming component, and / or! (2) starting materials for oxo dyes, and / or! (3) at least one direct dye, and / or! (4) at least one starting compound for dyes similar to natural. ! 3. The tool according to claim 1, characterized in that R1 in the compounds of formula (I) and R4 in the compounds of formula (II) are independently
Claims (14)
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE102006032315 | 2006-07-11 | ||
| DE102006032315.7 | 2006-07-11 | ||
| DE102006055675A DE102006055675A1 (en) | 2006-07-11 | 2006-11-23 | Hair Dye |
| DE102006055675.5 | 2006-11-23 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| RU2009104071A true RU2009104071A (en) | 2010-08-20 |
Family
ID=38556524
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| RU2009104071/15A RU2009104071A (en) | 2006-07-11 | 2007-07-10 | HAIR COLOR |
Country Status (4)
| Country | Link |
|---|---|
| EP (1) | EP2037870A1 (en) |
| DE (1) | DE102006055675A1 (en) |
| RU (1) | RU2009104071A (en) |
| WO (1) | WO2008006820A1 (en) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2010081942A1 (en) | 2008-12-05 | 2010-07-22 | Alex Hr Roustaei | Hydrogen cells or microcells with a hydrogen generator |
| JP5604789B2 (en) * | 2009-01-29 | 2014-10-15 | 株式会社オートネットワーク技術研究所 | Flame retardant, flame retardant resin composition and insulated wire |
| FR2956869B1 (en) | 2010-03-01 | 2014-05-16 | Alex Hr Roustaei | SYSTEM FOR PRODUCING HIGH CAPACITY FLEXIBLE FILM FOR PHOTOVOLTAIC AND OLED CELLS BY CYCLIC LAYER DEPOSITION |
| JP2020033495A (en) * | 2018-08-31 | 2020-03-05 | 保土谷化学工業株式会社 | Compound containing basic dye and amino acid, hair dye and hair dye composition |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR1353074A (en) * | 1962-01-26 | 1964-02-21 | Clairol International | Nitro-p-phenylenediamine derivatives and process for their preparation |
| FR2769223B1 (en) * | 1997-10-03 | 2003-08-22 | Oreal | OXIDIZING COMPOSITION AND USES FOR DYING, FOR PERMANENT DEFORMATION OR FOR DECOLORATION OF KERATINIC FIBERS |
| FR2782450B1 (en) * | 1998-08-19 | 2004-08-27 | Oreal | DYE COMPOSITION FOR KERATINIC FIBERS WITH A CATIONIC DIRECT DYE AND ANIONIC SURFACTANT |
| AU2024301A (en) * | 1999-12-20 | 2001-07-03 | Lion Corporation | Hair dye composition |
| US7166136B2 (en) * | 2001-01-09 | 2007-01-23 | Shiseido Company, Ltd. | Hairdye preparation |
| EP1820488A3 (en) * | 2006-02-16 | 2010-09-01 | The Procter & Gamble Company | Hair colouring compositions |
-
2006
- 2006-11-23 DE DE102006055675A patent/DE102006055675A1/en not_active Withdrawn
-
2007
- 2007-07-10 EP EP07787290A patent/EP2037870A1/en not_active Ceased
- 2007-07-10 RU RU2009104071/15A patent/RU2009104071A/en unknown
- 2007-07-10 WO PCT/EP2007/057015 patent/WO2008006820A1/en not_active Ceased
Also Published As
| Publication number | Publication date |
|---|---|
| EP2037870A1 (en) | 2009-03-25 |
| DE102006055675A1 (en) | 2008-01-17 |
| WO2008006820A1 (en) | 2008-01-17 |
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