CA1298787C - Composition utilises pour la modification permanente de la couleur des cheveux - Google Patents

Composition utilises pour la modification permanente de la couleur des cheveux

Info

Publication number: CA1298787C
Authority: CA; Canada
Prior art keywords: hair; composition; quaternized amino; amino lactam; lactam
Prior art date: 1986-10-24
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.): Expired - Fee Related

Application number

CA000548765A

Other languages

English (en)

Inventor

Michael W. Helioff

Carmen D. Bires

Robert B. Login

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.)

GAF Corp

Original Assignee

GAF Corp

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.)

1986-10-24

Filing date

1987-10-07

Publication date

1992-04-14

1986-10-24 Priority claimed from US06/922,923 external-priority patent/US4732990A/en

1987-06-10 Priority claimed from US07/060,284 external-priority patent/US4834767A/en

1987-10-07 Application filed by GAF Corp filed Critical GAF Corp

1992-04-14 Application granted granted Critical

1992-04-14 Publication of CA1298787C publication Critical patent/CA1298787C/fr

2009-04-14 Anticipated expiration legal-status Critical

Status Expired - Fee Related legal-status Critical Current

Links

239000000203 mixture Substances 0.000 title claims abstract description 84
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230000004075 alteration Effects 0.000 title abstract description 4
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-1 amino lactam Chemical class 0.000 claims abstract description 33
239000000975 dye Substances 0.000 claims abstract description 28
238000007254 oxidation reaction Methods 0.000 claims abstract description 13
230000003647 oxidation Effects 0.000 claims abstract description 11
125000004432 carbon atom Chemical group C* 0.000 claims abstract description 9
239000001024 permanent hair color Substances 0.000 claims abstract description 7
125000000217 alkyl group Chemical group 0.000 claims abstract description 6
239000003795 chemical substances by application Substances 0.000 claims abstract description 6
125000003118 aryl group Chemical group 0.000 claims abstract description 4
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims abstract description 3
CPELXLSAUQHCOX-UHFFFAOYSA-N Hydrogen bromide Chemical compound Br CPELXLSAUQHCOX-UHFFFAOYSA-N 0.000 claims abstract description 3
125000004183 alkoxy alkyl group Chemical group 0.000 claims abstract description 3
125000003545 alkoxy group Chemical group 0.000 claims abstract description 3
125000002877 alkyl aryl group Chemical group 0.000 claims abstract description 3
125000002947 alkylene group Chemical group 0.000 claims abstract description 3
125000003710 aryl alkyl group Chemical group 0.000 claims abstract description 3
239000003086 colorant Substances 0.000 claims abstract description 3
125000002768 hydroxyalkyl group Chemical group 0.000 claims abstract description 3
XMBWDFGMSWQBCA-UHFFFAOYSA-M iodide Chemical compound [I-] XMBWDFGMSWQBCA-UHFFFAOYSA-M 0.000 claims abstract description 3
238000009472 formulation Methods 0.000 claims description 37
238000000034 method Methods 0.000 claims description 28
230000008569 process Effects 0.000 claims description 27
150000003951 lactams Chemical class 0.000 claims description 24
238000004061 bleaching Methods 0.000 claims description 19
MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 claims description 18
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 12
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125000000913 palmityl 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])[H] 0.000 claims description 3
125000001421 myristyl 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])[H] 0.000 claims description 2
125000004079 stearyl 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])[H] 0.000 claims description 2
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XUMBMVFBXHLACL-UHFFFAOYSA-N Melanin Chemical compound O=C1C(=O)C(C2=CNC3=C(C(C(=O)C4=C32)=O)C)=C2C4=CNC2=C1C XUMBMVFBXHLACL-UHFFFAOYSA-N 0.000 abstract description 18
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238000002360 preparation method Methods 0.000 abstract description 4
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239000000543 intermediate Substances 0.000 description 17
ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 15
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 12
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JNYAEWCLZODPBN-JGWLITMVSA-N (2r,3r,4s)-2-[(1r)-1,2-dihydroxyethyl]oxolane-3,4-diol Chemical class OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O JNYAEWCLZODPBN-JGWLITMVSA-N 0.000 description 7
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 7
239000007844 bleaching agent Substances 0.000 description 7
239000004615 ingredient Substances 0.000 description 7
CBCKQZAAMUWICA-UHFFFAOYSA-N 1,4-phenylenediamine Chemical compound NC1=CC=C(N)C=C1 CBCKQZAAMUWICA-UHFFFAOYSA-N 0.000 description 6
VBICKXHEKHSIBG-UHFFFAOYSA-N 1-monostearoylglycerol Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(O)CO VBICKXHEKHSIBG-UHFFFAOYSA-N 0.000 description 6
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DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 6
229910000147 aluminium phosphate Inorganic materials 0.000 description 6
239000000908 ammonium hydroxide Substances 0.000 description 6
229960000541 cetyl alcohol Drugs 0.000 description 6
GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 description 6
238000012545 processing Methods 0.000 description 6
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IIZPXYDJLKNOIY-JXPKJXOSSA-N 1-palmitoyl-2-arachidonoyl-sn-glycero-3-phosphocholine Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCC\C=C/C\C=C/C\C=C/C\C=C/CCCCC IIZPXYDJLKNOIY-JXPKJXOSSA-N 0.000 description 4
FECNOIODIVNEKI-UHFFFAOYSA-N 2-[(2-aminobenzoyl)amino]benzoic acid Chemical class NC1=CC=CC=C1C(=O)NC1=CC=CC=C1C(O)=O FECNOIODIVNEKI-UHFFFAOYSA-N 0.000 description 4
235000019270 ammonium chloride Nutrition 0.000 description 4
238000004040 coloring Methods 0.000 description 4
230000003766 combability Effects 0.000 description 4
XVOYSCVBGLVSOL-UHFFFAOYSA-N cysteic acid Chemical compound OC(=O)C(N)CS(O)(=O)=O XVOYSCVBGLVSOL-UHFFFAOYSA-N 0.000 description 4
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UTXPMECBRCEYCI-UHFFFAOYSA-N 2-[2-[2-[2-(4-nonylphenoxy)ethoxy]ethoxy]ethoxy]ethanol Chemical compound CCCCCCCCCC1=CC=C(OCCOCCOCCOCCO)C=C1 UTXPMECBRCEYCI-UHFFFAOYSA-N 0.000 description 3
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125000000129 anionic group Chemical group 0.000 description 1
239000003963 antioxidant agent Substances 0.000 description 1
150000004982 aromatic amines Chemical class 0.000 description 1
239000004202 carbamide Substances 0.000 description 1
229910052799 carbon Inorganic materials 0.000 description 1
239000004359 castor oil Substances 0.000 description 1
235000019438 castor oil Nutrition 0.000 description 1
125000002091 cationic group Chemical group 0.000 description 1
239000003093 cationic surfactant Substances 0.000 description 1
238000006243 chemical reaction Methods 0.000 description 1
235000012000 cholesterol Nutrition 0.000 description 1
239000011248 coating agent Substances 0.000 description 1
238000000576 coating method Methods 0.000 description 1
239000006103 coloring component Substances 0.000 description 1
230000000536 complexating effect Effects 0.000 description 1
238000009833 condensation Methods 0.000 description 1
230000005494 condensation Effects 0.000 description 1
238000004132 cross linking Methods 0.000 description 1
125000000151 cysteine group Chemical group N[C@@H](CS)C(=O)* 0.000 description 1
238000004042 decolorization Methods 0.000 description 1
230000007812 deficiency Effects 0.000 description 1
230000002939 deleterious effect Effects 0.000 description 1
150000004985 diamines Chemical class 0.000 description 1
235000014113 dietary fatty acids Nutrition 0.000 description 1
230000003467 diminishing effect Effects 0.000 description 1
239000000982 direct dye Substances 0.000 description 1
235000019301 disodium ethylene diamine tetraacetate Nutrition 0.000 description 1
239000012153 distilled water Substances 0.000 description 1
238000009826 distribution Methods 0.000 description 1
239000003974 emollient agent Substances 0.000 description 1
239000000839 emulsion Substances 0.000 description 1
239000004318 erythorbic acid Substances 0.000 description 1
235000010350 erythorbic acid Nutrition 0.000 description 1
150000002169 ethanolamines Chemical class 0.000 description 1
BEFDCLMNVWHSGT-UHFFFAOYSA-N ethenylcyclopentane Chemical compound C=CC1CCCC1 BEFDCLMNVWHSGT-UHFFFAOYSA-N 0.000 description 1
239000000194 fatty acid Substances 0.000 description 1
229930195729 fatty acid Natural products 0.000 description 1
150000004665 fatty acids Chemical class 0.000 description 1
229960005150 glycerol Drugs 0.000 description 1
ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 1
230000003700 hair damage Effects 0.000 description 1
210000003780 hair follicle Anatomy 0.000 description 1
230000003779 hair growth Effects 0.000 description 1
210000004919 hair shaft Anatomy 0.000 description 1
229910001385 heavy metal Inorganic materials 0.000 description 1
XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
235000019447 hydroxyethyl cellulose Nutrition 0.000 description 1
150000002500 ions Chemical class 0.000 description 1
229940026239 isoascorbic acid Drugs 0.000 description 1
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
238000002386 leaching Methods 0.000 description 1
239000007788 liquid Substances 0.000 description 1
239000011159 matrix material Substances 0.000 description 1
239000003607 modifier Substances 0.000 description 1
150000004780 naphthols Chemical class 0.000 description 1
230000003472 neutralizing effect Effects 0.000 description 1
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
229910052757 nitrogen Inorganic materials 0.000 description 1
229940055577 oleyl alcohol Drugs 0.000 description 1
XMLQWXUVTXCDDL-UHFFFAOYSA-N oleyl alcohol Natural products CCCCCCC=CCCCCCCCCCCO XMLQWXUVTXCDDL-UHFFFAOYSA-N 0.000 description 1
125000001117 oleyl 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])=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 description 1
238000010525 oxidative degradation reaction Methods 0.000 description 1
ATGUVEKSASEFFO-UHFFFAOYSA-N p-aminodiphenylamine Chemical compound C1=CC(N)=CC=C1NC1=CC=CC=C1 ATGUVEKSASEFFO-UHFFFAOYSA-N 0.000 description 1
229910052697 platinum Inorganic materials 0.000 description 1
229920001223 polyethylene glycol Polymers 0.000 description 1
229920001184 polypeptide Polymers 0.000 description 1
150000008442 polyphenolic compounds Polymers 0.000 description 1
239000011591 potassium Chemical class 0.000 description 1
229910052700 potassium Inorganic materials 0.000 description 1
239000012286 potassium permanganate Substances 0.000 description 1
USHAGKDGDHPEEY-UHFFFAOYSA-L potassium persulfate Chemical compound [K+].[K+].[O-]S(=O)(=O)OOS([O-])(=O)=O USHAGKDGDHPEEY-UHFFFAOYSA-L 0.000 description 1
239000002243 precursor Substances 0.000 description 1
230000002028 premature Effects 0.000 description 1
125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
102000004196 processed proteins & peptides Human genes 0.000 description 1
108090000765 processed proteins & peptides Proteins 0.000 description 1
235000018102 proteins Nutrition 0.000 description 1
108090000623 proteins and genes Proteins 0.000 description 1
102000004169 proteins and genes Human genes 0.000 description 1
150000003222 pyridines Chemical class 0.000 description 1
150000004040 pyrrolidinones Chemical class 0.000 description 1
125000004929 pyrrolidonyl group Chemical group N1(C(CCC1)=O)* 0.000 description 1
UKHVLWKBNNSRRR-TYYBGVCCSA-M quaternium-15 Chemical compound [Cl-].C1N(C2)CN3CN2C[N+]1(C/C=C/Cl)C3 UKHVLWKBNNSRRR-TYYBGVCCSA-M 0.000 description 1
229940096792 quaternium-15 Drugs 0.000 description 1
230000009257 reactivity Effects 0.000 description 1
238000011084 recovery Methods 0.000 description 1
230000009467 reduction Effects 0.000 description 1
238000007086 side reaction Methods 0.000 description 1
230000036556 skin irritation Effects 0.000 description 1
231100000475 skin irritation Toxicity 0.000 description 1
229910000029 sodium carbonate Inorganic materials 0.000 description 1
JVBXVOWTABLYPX-UHFFFAOYSA-L sodium dithionite Chemical compound [Na+].[Na+].[O-]S(=O)S([O-])=O JVBXVOWTABLYPX-UHFFFAOYSA-L 0.000 description 1
235000010267 sodium hydrogen sulphite Nutrition 0.000 description 1
235000019795 sodium metasilicate Nutrition 0.000 description 1
CHQMHPLRPQMAMX-UHFFFAOYSA-L sodium persulfate Substances [Na+].[Na+].[O-]S(=O)(=O)OOS([O-])(=O)=O CHQMHPLRPQMAMX-UHFFFAOYSA-L 0.000 description 1
NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 1
229910052911 sodium silicate Inorganic materials 0.000 description 1
238000005063 solubilization Methods 0.000 description 1
230000007928 solubilization Effects 0.000 description 1
239000002904 solvent Substances 0.000 description 1
235000010199 sorbic acid Nutrition 0.000 description 1
239000004334 sorbic acid Substances 0.000 description 1
229940075582 sorbic acid Drugs 0.000 description 1
239000003381 stabilizer Substances 0.000 description 1
238000003860 storage Methods 0.000 description 1
125000001424 substituent group Chemical group 0.000 description 1
239000000271 synthetic detergent Substances 0.000 description 1
239000003784 tall oil Substances 0.000 description 1
230000008719 thickening Effects 0.000 description 1
239000002562 thickening agent Substances 0.000 description 1
239000010409 thin film Substances 0.000 description 1
150000003573 thiols Chemical class 0.000 description 1
FYOWZTWVYZOZSI-UHFFFAOYSA-N thiourea dioxide Chemical compound NC(=N)S(O)=O FYOWZTWVYZOZSI-UHFFFAOYSA-N 0.000 description 1
238000009827 uniform distribution Methods 0.000 description 1
AQLJVWUFPCUVLO-UHFFFAOYSA-N urea hydrogen peroxide Chemical compound OO.NC(N)=O AQLJVWUFPCUVLO-UHFFFAOYSA-N 0.000 description 1
238000009736 wetting Methods 0.000 description 1

Classifications

- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M16/00—Biochemical treatment of fibres, threads, yarns, fabrics, or fibrous goods made from such materials, e.g. enzymatic
- 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
- A61K8/4906—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with one nitrogen as the only hetero atom
- A61K8/4913—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with one nitrogen as the only hetero atom having five membered rings, e.g. pyrrolidone carboxylic acid
- 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
- A61Q5/08—Preparations for bleaching the hair
- 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)
Public Health (AREA)
Veterinary Medicine (AREA)
Animal Behavior & Ethology (AREA)
General Health & Medical Sciences (AREA)
Chemical & Material Sciences (AREA)
Epidemiology (AREA)
Birds (AREA)
Biochemistry (AREA)
Chemical Kinetics & Catalysis (AREA)
General Chemical & Material Sciences (AREA)
Microbiology (AREA)
Engineering & Computer Science (AREA)
Textile Engineering (AREA)
Cosmetics (AREA)

CA000548765A 1986-10-24 1987-10-07 Composition utilises pour la modification permanente de la couleur des cheveux Expired - Fee Related CA1298787C (fr)

Applications Claiming Priority (4)

Application Number	Priority Date	Filing Date	Title
US922,923		1986-10-24
US06/922,923 US4732990A (en)	1986-10-24	1986-10-24	Quaternized nitrogen containing compounds
US07/060,284 US4834767A (en)	1987-06-10	1987-06-10	Compositions used in permanent alteration of hair color
US60,284		1987-06-10

Publications (1)

Publication Number	Publication Date
CA1298787C true CA1298787C (fr)	1992-04-14

Family

ID=26739776

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CA000548765A Expired - Fee Related CA1298787C (fr)	1986-10-24	1987-10-07	Composition utilises pour la modification permanente de la couleur des cheveux

Country Status (8)

Country	Link
EP (1)	EP0288553A4 (fr)
JP (1)	JPH01501003A (fr)
AU (1)	AU597454B2 (fr)
CA (1)	CA1298787C (fr)
DK (1)	DK350488A (fr)
IL (1)	IL84085A (fr)
NO (1)	NO882650L (fr)
WO (1)	WO1988003017A1 (fr)

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US5157075A (en) *	1990-05-02	1992-10-20	Taenaka Mining Co., Ltd.	Modified melanin
DE60227490D1 (de) *	2001-03-30	2008-08-21	Procter & Gamble	Haarbleichmittel
EP1300136A3 (fr) *	2001-10-04	2003-05-14	Henkel Kommanditgesellschaft auf Aktien	Méthode pour changer la coloration des cheveux à base de sels de dithionite
US6709468B2 (en)	2002-03-07	2004-03-23	Unilever Home & Personal Care Usa	Gradual permanent coloring of hair using dye intermediates in alkaline water which contains quaternary ammonium compounds
FR2889660B1 (fr) *	2005-08-11	2007-10-19	Oreal	Composition de coloration des fibres keratiniques comprenant au moins une base d'oxydation et un ester de sorbitan polyoxyethylene particulier
DE102005059647A1 (de) *	2005-12-12	2007-06-14	Henkel Kgaa	Bleichmittel
EP2260077B1 (fr) *	2008-03-10	2012-04-25	Perachem Limited	Composition et procédés de traitement capillaire
FR3015272B1 (fr) *	2013-12-19	2016-01-08	Oreal	Procede de coloration mettant en œuvre des compositions riches en corps gras

Family Cites Families (19)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US2945863A (en) *	1958-06-24	1960-07-19	Gen Aniline & Film Corp	Amides of aminoalkyl pyrrolidones
NL120222C (fr) *	1960-04-15
US3145147A (en) *	1961-02-20	1964-08-18	Gen Aniline & Film Corp	Film forming composition of copolymers of nu-vinyl-epsilon-caprolactam
US3138610A (en) *	1961-03-10	1964-06-23	Gen Aniline & Film Corp	Substituted imidazolines
FR1326561A (fr) *	1962-03-29	1963-05-10	Oreal	Adjuvant pour fixateur de permanente
US3910862A (en) *	1970-01-30	1975-10-07	Gaf Corp	Copolymers of vinyl pyrrolidone containing quarternary ammonium groups
US3914403A (en) *	1973-05-11	1975-10-21	Gaf Corp	Hair care preparations containing N-vinyl pyrrolidone homo- and copolymers and a quaternized copolymer of vinyl pyrrolidone
AT365448B (de) *	1975-07-04	1982-01-11	Oreal	Kosmetische zubereitung
US4532127A (en) *	1976-02-09	1985-07-30	Clairol Incorporated	Composition for lightening or coloring hair containing an oxidizing agent and certain quaternary amines
US4035478A (en) *	1976-03-08	1977-07-12	American Cyanamid Company	Clear, water-white hair conditioning composition
LU81694A1 (fr) *	1979-09-17	1981-04-17	Oreal	Composition contenant des derives d'ammonium bis quaternaires a deux chaines lipophiles destinee au traitement de matieres keratiniques et composes nouveaux utilises
FR2502949B1 (fr) *	1981-04-02	1985-10-18	Oreal	Procede de preparation d'une composition de teinture ou de decoloration des cheveux, composition destinee a la mise en oeuvre de ce procede, et application de la composition obtenue par le procede
LU83911A1 (fr) *	1982-01-29	1983-09-02	Oreal	Produit nettoyant des cheveux et de la peau a base d'acylise thionates et de polymeres cationiques
LU83949A1 (fr) *	1982-02-16	1983-09-02	Oreal	Composition destinee au traitement des matieres keratiniques contenant au moins un polymere cationique et au moins un latex anionique
FR2530141A1 (fr) *	1982-07-13	1984-01-20	Oreal	Procede de mise en plis des cheveux et composition cosmetique pour sa mise en oeuvre
US4534877A (en) *	1982-07-30	1985-08-13	The Procter & Gamble Company	Shampoo compositions comprising specific betaine surfactants and a quaternary compound
US4457912A (en) *	1982-08-24	1984-07-03	Scodari Nicholas F	Electric razor preshave composition
FR2553779B1 (fr) *	1983-10-19	1986-02-21	Hoechst France	Tetrapolymeres ampholytes cationiques, leur application dans le traitement des fibres keratiniques et les compositions les renfermant
US4732990A (en) *	1986-10-24	1988-03-22	Gaf Corporation	Quaternized nitrogen containing compounds

1987
- 1987-09-24 JP JP63500122A patent/JPH01501003A/ja active Pending
- 1987-09-24 AU AU82785/87A patent/AU597454B2/en not_active Ceased
- 1987-09-24 EP EP19870907847 patent/EP0288553A4/en not_active Withdrawn
- 1987-09-24 WO PCT/US1987/002457 patent/WO1988003017A1/fr not_active Ceased
- 1987-10-04 IL IL84085A patent/IL84085A/xx not_active IP Right Cessation
- 1987-10-07 CA CA000548765A patent/CA1298787C/fr not_active Expired - Fee Related
1988
- 1988-06-15 NO NO882650A patent/NO882650L/no unknown
- 1988-06-24 DK DK350488A patent/DK350488A/da not_active Application Discontinuation

Also Published As

Publication number	Publication date
IL84085A0 (en)	1988-03-31
JPH01501003A (ja)	1989-04-06
IL84085A (en)	1993-05-13
AU8278587A (en)	1988-05-25
NO882650D0 (no)	1988-06-15
EP0288553A1 (fr)	1988-11-02
DK350488D0 (da)	1988-06-24
NO882650L (no)	1988-06-15
EP0288553A4 (en)	1991-08-07
DK350488A (da)	1988-06-24
AU597454B2 (en)	1990-05-31
WO1988003017A1 (fr)	1988-05-05

Legal Events

Date	Code	Title	Description
1994-10-14	MKLA	Lapsed

Publication	Publication Date	Title
US4834767A (en)	1989-05-30	Compositions used in permanent alteration of hair color
EP0052489B1 (fr)	1985-07-24	Dérivés cationiques de la kératine, procédé pour leur fabrication et produits cosmétiques pour le traitement des cheveux contenant ceux-ci
US5628991A (en)	1997-05-13	Cosmetic composition containing a diaminoalkane as an odorless alkalifying agent
DE60217850T2 (de)	2007-11-15	Zweiteilige wässrige zusammensetzung für die oxidative haarfärbung
AU599116B2 (en)	1990-07-12	Compositions used in permanent alteration of hair color
CA1258637A (fr)	1989-08-22	Composes utilises pour alterer de facon permanente la structure des cheveux
WO1999037278A1 (fr)	1999-07-29	Composition pour la coloration de fibres keratiniques depourvue d'ammoniaque
JPS59106413A (ja)	1984-06-20	酸化染毛剤
WO1989010115A1 (fr)	1989-11-02	Additifs de traitement des cheveux
JP2021080201A (ja)	2021-05-27	多剤式酸化染毛剤用の第１剤及び多剤式酸化染毛剤
AU597454B2 (en)	1990-05-31	Composition used in permanent alteration of hair colour comprising quaternized amino lactam
US4957731A (en)	1990-09-18	Hair processing additives
CA2145860A1 (fr)	1994-04-14	Preparations pour le traitement des cheveux
JP2000264822A (ja)	2000-09-26	染毛剤組成物
JP2001114657A (ja)	2001-04-24	染毛剤組成物
JP2860361B2 (ja)	1999-02-24	染毛剤
JPH04312514A (ja)	1992-11-04	染毛剤
JPH0471885B2 (fr)	1992-11-16
JP2686696B2 (ja)	1997-12-08	染毛剤
KR20250090737A (ko)	2025-06-20	겔타입의 모발염색용 조성물 및 그 제조방법
JP2001288053A (ja)	2001-10-16	染毛剤組成物
JPH0463104B2 (fr)	1992-10-08
JPH02138206A (ja)	1990-05-28	染毛剤組成物
EA053054B1 (ru)	2026-04-13	Активный комплекс для приготовления композиций для ухода за поврежденными волосами
JPH02231413A (ja)	1990-09-13	染毛剤組成物