CH621256A5 - Hair dyeing composition - Google Patents

Hair dyeing composition Download PDF

Info

Publication number: CH621256A5
Authority: CH; Switzerland
Prior art keywords: coupler; developer; hair dye; hair; aminophenol
Prior art date: 1975-03-03

Application number

CH265876A

Other languages

German (de)

English (en)

Inventor

David Dr Rose

Ferdi Dr Saygin

Edgar Lieske

Original Assignee

Henkel Kgaa

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.)

1975-03-03

Filing date

1976-03-03

Publication date

1981-01-30

1976-03-03 Application filed by Henkel Kgaa filed Critical Henkel Kgaa

1981-01-30 Publication of CH621256A5 publication Critical patent/CH621256A5/de

Links

238000004043 dyeing Methods 0.000 title description 9
239000000203 mixture Substances 0.000 title description 5
239000000118 hair dye Substances 0.000 claims description 17
CWLKGDAVCFYWJK-UHFFFAOYSA-N 3-aminophenol Chemical class NC1=CC=CC(O)=C1 CWLKGDAVCFYWJK-UHFFFAOYSA-N 0.000 claims description 15
239000000126 substance Substances 0.000 claims description 14
FWUALUHYKLDYAN-UHFFFAOYSA-N 3-amino-4-chlorophenol Chemical compound NC1=CC(O)=CC=C1Cl FWUALUHYKLDYAN-UHFFFAOYSA-N 0.000 claims description 11
230000003647 oxidation Effects 0.000 claims description 10
238000007254 oxidation reaction Methods 0.000 claims description 10
239000000975 dye Substances 0.000 claims description 8
125000004433 nitrogen atom Chemical group N* 0.000 claims description 8
229910052757 nitrogen Inorganic materials 0.000 claims description 7
239000003795 chemical substances by application Substances 0.000 claims description 6
125000004432 carbon atom Chemical group C* 0.000 claims description 5
125000000623 heterocyclic group Chemical group 0.000 claims description 5
150000003839 salts Chemical class 0.000 claims description 5
229910052801 chlorine Inorganic materials 0.000 claims description 4
239000001257 hydrogen Substances 0.000 claims description 4
229910052739 hydrogen Inorganic materials 0.000 claims description 4
125000004430 oxygen atom Chemical group O* 0.000 claims description 4
PZRKPUQWIFJRKZ-UHFFFAOYSA-N pyrimidine-2,4,5,6-tetramine Chemical compound NC1=NC(N)=C(N)C(N)=N1 PZRKPUQWIFJRKZ-UHFFFAOYSA-N 0.000 claims description 4
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 3
239000000460 chlorine Substances 0.000 claims description 3
125000004435 hydrogen atom Chemical class [H]* 0.000 claims description 3
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 3
ISPYQTSUDJAMAB-UHFFFAOYSA-N 2-chlorophenol Chemical group OC1=CC=CC=C1Cl ISPYQTSUDJAMAB-UHFFFAOYSA-N 0.000 claims description 2
239000000982 direct dye Substances 0.000 claims description 2
125000005843 halogen group Chemical group 0.000 claims description 2
229940018563 3-aminophenol Drugs 0.000 claims 1
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 1
125000001424 substituent group Chemical group 0.000 claims 1
239000000839 emulsion Substances 0.000 description 8
238000002360 preparation method Methods 0.000 description 8
MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 6
150000001875 compounds Chemical class 0.000 description 6
239000007800 oxidant agent Substances 0.000 description 6
CFWIOOCJVYJEID-UHFFFAOYSA-N 3-amino-2-chlorophenol Chemical compound NC1=CC=CC(O)=C1Cl CFWIOOCJVYJEID-UHFFFAOYSA-N 0.000 description 5
239000006071 cream Substances 0.000 description 5
238000005691 oxidative coupling reaction Methods 0.000 description 5
PLIKAWJENQZMHA-UHFFFAOYSA-N 4-aminophenol Chemical compound NC1=CC=C(O)C=C1 PLIKAWJENQZMHA-UHFFFAOYSA-N 0.000 description 4
-1 heterocyclic hydrazones Chemical class 0.000 description 4
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
OBCSAIDCZQSFQH-UHFFFAOYSA-N 2-methyl-1,4-phenylenediamine Chemical compound CC1=CC(N)=CC=C1N OBCSAIDCZQSFQH-UHFFFAOYSA-N 0.000 description 3
125000003277 amino group Chemical group 0.000 description 3
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 3
239000001045 blue dye Substances 0.000 description 3
238000004040 coloring Methods 0.000 description 3
230000000694 effects Effects 0.000 description 3
150000002191 fatty alcohols Chemical class 0.000 description 3
239000000499 gel Substances 0.000 description 3
230000037308 hair color Effects 0.000 description 3
238000000034 method Methods 0.000 description 3
229910052760 oxygen Inorganic materials 0.000 description 3
239000001301 oxygen Substances 0.000 description 3
230000002110 toxicologic effect Effects 0.000 description 3
231100000027 toxicology Toxicity 0.000 description 3
GHOKWGTUZJEAQD-ZETCQYMHSA-N (D)-(+)-Pantothenic acid Chemical compound OCC(C)(C)[C@@H](O)C(=O)NCCC(O)=O GHOKWGTUZJEAQD-ZETCQYMHSA-N 0.000 description 2
CBCKQZAAMUWICA-UHFFFAOYSA-N 1,4-phenylenediamine Chemical compound NC1=CC=C(N)C=C1 CBCKQZAAMUWICA-UHFFFAOYSA-N 0.000 description 2
DFMDAJMTLJGKFW-UHFFFAOYSA-N 3-chloro-2-nitrophenol Chemical compound OC1=CC=CC(Cl)=C1[N+]([O-])=O DFMDAJMTLJGKFW-UHFFFAOYSA-N 0.000 description 2
XSFKCGABINPZRK-UHFFFAOYSA-N 4-aminopyrazol-3-one Chemical class NC1=CN=NC1=O XSFKCGABINPZRK-UHFFFAOYSA-N 0.000 description 2
QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
BZORFPDSXLZWJF-UHFFFAOYSA-N N,N-dimethyl-1,4-phenylenediamine Chemical compound CN(C)C1=CC=C(N)C=C1 BZORFPDSXLZWJF-UHFFFAOYSA-N 0.000 description 2
229910019142 PO4 Inorganic materials 0.000 description 2
XBDQKXXYIPTUBI-UHFFFAOYSA-N Propionic acid Chemical class CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 2
150000001242 acetic acid derivatives Chemical class 0.000 description 2
239000000654 additive Substances 0.000 description 2
150000001805 chlorine compounds Chemical class 0.000 description 2
HVYWMOMLDIMFJA-DPAQBDIFSA-N cholesterol Chemical compound C1C=C2C[C@@H](O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H]([C@H](C)CCCC(C)C)[C@@]1(C)CC2 HVYWMOMLDIMFJA-DPAQBDIFSA-N 0.000 description 2
150000001860 citric acid derivatives Chemical class 0.000 description 2
239000003086 colorant Substances 0.000 description 2
235000014113 dietary fatty acids Nutrition 0.000 description 2
239000003995 emulsifying agent Substances 0.000 description 2
239000000194 fatty acid Substances 0.000 description 2
229930195729 fatty acid Natural products 0.000 description 2
150000004665 fatty acids Chemical class 0.000 description 2
125000000524 functional group Chemical group 0.000 description 2
150000003893 lactate salts Chemical class 0.000 description 2
150000007522 mineralic acids Chemical class 0.000 description 2
150000007524 organic acids Chemical class 0.000 description 2
235000005985 organic acids Nutrition 0.000 description 2
230000001590 oxidative effect Effects 0.000 description 2
235000021317 phosphate Nutrition 0.000 description 2
150000003013 phosphoric acid derivatives Chemical class 0.000 description 2
XXQBEVHPUKOQEO-UHFFFAOYSA-N potassium superoxide Chemical compound [K+].[K+].[O-][O-] XXQBEVHPUKOQEO-UHFFFAOYSA-N 0.000 description 2
ZZYXNRREDYWPLN-UHFFFAOYSA-N pyridine-2,3-diamine Chemical class NC1=CC=CN=C1N ZZYXNRREDYWPLN-UHFFFAOYSA-N 0.000 description 2
CSNFMBGHUOSBFU-UHFFFAOYSA-N pyrimidine-2,4,5-triamine Chemical compound NC1=NC=C(N)C(N)=N1 CSNFMBGHUOSBFU-UHFFFAOYSA-N 0.000 description 2
239000002453 shampoo Substances 0.000 description 2
150000003467 sulfuric acid derivatives Chemical class 0.000 description 2
239000002562 thickening agent Substances 0.000 description 2
238000009736 wetting Methods 0.000 description 2
239000000080 wetting agent Substances 0.000 description 2
150000005207 1,3-dihydroxybenzenes Chemical class 0.000 description 1
HISHUMDTGXICEZ-UHFFFAOYSA-N 1-chloro-4-methoxy-2-nitrobenzene Chemical compound COC1=CC=C(Cl)C([N+]([O-])=O)=C1 HISHUMDTGXICEZ-UHFFFAOYSA-N 0.000 description 1
JTTIOYHBNXDJOD-UHFFFAOYSA-N 2,4,6-triaminopyrimidine Chemical class NC1=CC(N)=NC(N)=N1 JTTIOYHBNXDJOD-UHFFFAOYSA-N 0.000 description 1
GBOUQGUQUUPGLO-UHFFFAOYSA-N 2-chloro-5-methoxyaniline Chemical compound COC1=CC=C(Cl)C(N)=C1 GBOUQGUQUUPGLO-UHFFFAOYSA-N 0.000 description 1
HGUYBLVGLMAUFF-UHFFFAOYSA-N 2-methoxybenzene-1,4-diamine Chemical compound COC1=CC(N)=CC=C1N HGUYBLVGLMAUFF-UHFFFAOYSA-N 0.000 description 1
JOBPGDXYRPFRIV-UHFFFAOYSA-N 3-amino-5-chlorophenol Chemical compound NC1=CC(O)=CC(Cl)=C1 JOBPGDXYRPFRIV-UHFFFAOYSA-N 0.000 description 1
GHOKWGTUZJEAQD-UHFFFAOYSA-N Chick antidermatitis factor Natural products OCC(C)(C)C(O)C(=O)NCCC(O)=O GHOKWGTUZJEAQD-UHFFFAOYSA-N 0.000 description 1
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
229920000877 Melamine resin Polymers 0.000 description 1
239000005662 Paraffin oil Substances 0.000 description 1
229920002472 Starch Polymers 0.000 description 1
XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
230000002378 acidificating effect Effects 0.000 description 1
230000000996 additive effect Effects 0.000 description 1
125000000217 alkyl group Chemical group 0.000 description 1
229940045714 alkyl sulfonate alkylating agent Drugs 0.000 description 1
150000008052 alkyl sulfonates Chemical class 0.000 description 1
125000004414 alkyl thio group Chemical group 0.000 description 1
150000001408 amides Chemical class 0.000 description 1
150000001412 amines Chemical class 0.000 description 1
229910021529 ammonia Inorganic materials 0.000 description 1
229940051880 analgesics and antipyretics pyrazolones Drugs 0.000 description 1
125000000129 anionic group Chemical group 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
229910021538 borax Inorganic materials 0.000 description 1
239000004202 carbamide Substances 0.000 description 1
125000001309 chloro group Chemical group Cl* 0.000 description 1
WCTXJBYIXVVFCF-UHFFFAOYSA-M chlorotin Chemical compound [Sn]Cl WCTXJBYIXVVFCF-UHFFFAOYSA-M 0.000 description 1
235000012000 cholesterol Nutrition 0.000 description 1
239000000470 constituent Substances 0.000 description 1
239000002537 cosmetic Substances 0.000 description 1
230000006735 deficit Effects 0.000 description 1
229910003460 diamond Inorganic materials 0.000 description 1
239000010432 diamond Substances 0.000 description 1
VFNGKCDDZUSWLR-UHFFFAOYSA-L disulfate(2-) Chemical compound [O-]S(=O)(=O)OS([O-])(=O)=O VFNGKCDDZUSWLR-UHFFFAOYSA-L 0.000 description 1
229910052731 fluorine Inorganic materials 0.000 description 1
125000001153 fluoro group Chemical group F* 0.000 description 1
150000002391 heterocyclic compounds Chemical class 0.000 description 1
150000004988 m-phenylenediamines Chemical class 0.000 description 1
JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 1
229920000609 methyl cellulose Polymers 0.000 description 1
239000001923 methylcellulose Substances 0.000 description 1
235000010981 methylcellulose Nutrition 0.000 description 1
150000004780 naphthols Chemical class 0.000 description 1
230000007935 neutral effect Effects 0.000 description 1
230000009935 nitrosation Effects 0.000 description 1
238000007034 nitrosation reaction Methods 0.000 description 1
RBXVOQPAMPBADW-UHFFFAOYSA-N nitrous acid;phenol Chemical class ON=O.OC1=CC=CC=C1 RBXVOQPAMPBADW-UHFFFAOYSA-N 0.000 description 1
239000003921 oil Substances 0.000 description 1
239000003973 paint Substances 0.000 description 1
229940055726 pantothenic acid Drugs 0.000 description 1
235000019161 pantothenic acid Nutrition 0.000 description 1
239000011713 pantothenic acid Substances 0.000 description 1
239000002304 perfume Substances 0.000 description 1
150000002989 phenols Chemical class 0.000 description 1
125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
150000003142 primary aromatic amines Chemical class 0.000 description 1
JEXVQSWXXUJEMA-UHFFFAOYSA-N pyrazol-3-one Chemical class O=C1C=CN=N1 JEXVQSWXXUJEMA-UHFFFAOYSA-N 0.000 description 1
150000003230 pyrimidines Chemical class 0.000 description 1
125000000714 pyrimidinyl group Chemical group 0.000 description 1
159000000000 sodium salts Chemical group 0.000 description 1
235000010339 sodium tetraborate Nutrition 0.000 description 1
239000008107 starch Substances 0.000 description 1
235000019698 starch Nutrition 0.000 description 1
238000003786 synthesis reaction Methods 0.000 description 1
BSVBQGMMJUBVOD-UHFFFAOYSA-N trisodium borate Chemical compound [Na+].[Na+].[Na+].[O-]B([O-])[O-] BSVBQGMMJUBVOD-UHFFFAOYSA-N 0.000 description 1

Classifications

- 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
- A61K8/4953—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 containing pyrimidine ring derivatives, e.g. minoxidil
- 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

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)

CH265876A 1975-03-03 1976-03-03 Hair dyeing composition CH621256A5 (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE19752509152 DE2509152C2 (de)	1975-03-03	1975-03-03	Haarfärbemittel

Publications (1)

Publication Number	Publication Date
CH621256A5 true CH621256A5 (en)	1981-01-30

Family

ID=5940316

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CH265876A CH621256A5 (en)	1975-03-03	1976-03-03	Hair dyeing composition

Country Status (8)

Country	Link
AT (1)	AT342785B (it)
BE (1)	BE839128A (it)
CH (1)	CH621256A5 (it)
DE (1)	DE2509152C2 (it)
FR (1)	FR2302726A1 (it)
GB (1)	GB1530686A (it)
IT (1)	IT1055472B (it)
NL (1)	NL184255C (it)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE2935429A1 (de) *	1979-09-01	1981-03-26	Henkel KGaA, 40589 Düsseldorf	Haarfaerbemittel
DE3016905A1 (de) *	1980-05-02	1981-11-05	Henkel KGaA, 4000 Düsseldorf	Haarfaerbemittel
DE3524329A1 (de) *	1985-07-08	1987-01-08	Henkel Kgaa	Neue aminophenole und deren verwendung in oxidationshaarfaerbemitteln
DE19962872A1 (de) *	1999-12-24	2001-06-28	Henkel Kgaa	Mittel zum Färben von keratinhaltigen Fasern

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE1949749C3 (de) *	1969-10-02	1978-06-01	Henkel & Kgaa, 4000 Duesseldorf	Mittel zum Färben menschlicher Haare
LU67861A1 (it) *	1973-06-22	1975-03-27

1975
- 1975-03-03 DE DE19752509152 patent/DE2509152C2/de not_active Expired
1976
- 1976-02-11 NL NL7601399A patent/NL184255C/xx not_active IP Right Cessation
- 1976-02-27 IT IT2064276A patent/IT1055472B/it active
- 1976-03-02 GB GB819776A patent/GB1530686A/en not_active Expired
- 1976-03-02 AT AT153876A patent/AT342785B/de not_active IP Right Cessation
- 1976-03-03 FR FR7606024A patent/FR2302726A1/fr active Granted
- 1976-03-03 BE BE164801A patent/BE839128A/xx not_active IP Right Cessation
- 1976-03-03 CH CH265876A patent/CH621256A5/de not_active IP Right Cessation

Also Published As

Publication number	Publication date
FR2302726A1 (fr)	1976-10-01
DE2509152C2 (de)	1985-01-10
DE2509152A1 (de)	1976-09-09
FR2302726B1 (it)	1979-08-24
NL184255C (nl)	1989-06-01
GB1530686A (en)	1978-11-01
NL7601399A (nl)	1976-09-07
AT342785B (de)	1978-04-25
NL184255B (nl)	1989-01-02
IT1055472B (it)	1981-12-21
BE839128A (fr)	1976-09-03
ATA153876A (de)	1977-08-15

Legal Events

Date	Code	Title	Description
1991-11-29	PL	Patent ceased
2024-10-31	PL	Patent ceased

Publication	Publication Date	Title
EP0030680B1 (de)	1983-08-24	Haarfärbemittel
CH632925A5 (de)	1982-11-15	Haarfaerbemittel.
DE2715680A1 (de)	1978-10-12	Haarfaerbemittel
DE2509096C2 (de)	1986-03-27	Haarfärbemittel auf der Basis von Oxidationsfarbstoffen und 2,4-Dichlor-3-aminophenol
DE3016008A1 (de)	1981-10-29	Neue kupplerkomponenten fuer oxidationshaarfarben, deren herstellung und verwendung, sowie diese enthaltende haarfaerbemittel
EP0063736B1 (de)	1986-01-08	Verwendung von Dihydroxypyridinen als Kupplerkomponente in Oxidationshaarfarbstoffen und Haarfärbemittel
DE2834605C2 (it)	1988-11-10
DE2714831A1 (de)	1978-10-12	Haarfaerbemittel
DE2702118B2 (de)	1980-08-07	Haarfärbemittel
DE2813076C2 (de)	1986-10-16	Haarfärbemittel
DE2632810A1 (de)	1978-01-26	Haarfaerbemittel
EP0079540B1 (de)	1985-03-20	Haarfärbemittel
DE2934330A1 (de)	1981-03-12	Haarfaerbemittel.
EP0002828B1 (de)	1982-01-06	Haarfärbemittel
EP0004368B1 (de)	1981-11-04	Haarfärbemittel
EP0137524B1 (de)	1988-01-20	Mittel zum Färben von Haaren
DE2629805C2 (de)	1985-11-28	Haarfärbemittel
DE2706029C2 (de)	1985-10-31	Haarfärbemittel
DE2509152C2 (de)	1985-01-10	Haarfärbemittel
DE2934329C2 (it)	1988-02-04
DE2719424A1 (de)	1978-11-09	Haarfaerbemittel
EP0024710A2 (de)	1981-03-11	Haarfärbemittel
DE2623563A1 (de)	1977-12-15	Haarfaerbemittel
DE2932800C2 (it)	1988-02-04
EP0039807A2 (de)	1981-11-18	Haarfärbemittel