SK145599A3 - Use of unsaturated aldehydes in dying fibers containing keratin - Google Patents

Use of unsaturated aldehydes in dying fibers containing keratin Download PDF

Info

Publication number: SK145599A3
Authority: SK; Slovakia
Prior art keywords: amino; acid; methyl; hydroxy; diamino
Prior art date: 1997-04-24

Application number

SK1455-99A

Other languages

English (en)

Slovak (sk)

Inventor

Hinrich Moller

Horst Hoffkes

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.)

1997-04-24

Filing date

1998-04-16

Publication date

2000-05-16

1998-04-16 Application filed by Henkel Kgaa filed Critical Henkel Kgaa

2000-05-16 Publication of SK145599A3 publication Critical patent/SK145599A3/sk

Links

239000000835 fiber Substances 0.000 title claims abstract description 27
102000011782 Keratins Human genes 0.000 title claims abstract description 24
108010076876 Keratins Proteins 0.000 title claims abstract description 24
150000001299 aldehydes Chemical class 0.000 title claims description 23
210000004209 hair Anatomy 0.000 claims abstract description 16
229910052739 hydrogen Inorganic materials 0.000 claims abstract description 8
239000001257 hydrogen Substances 0.000 claims abstract description 7
150000002431 hydrogen Chemical class 0.000 claims abstract description 6
150000005840 aryl radicals Chemical class 0.000 claims abstract description 5
229910052736 halogen Inorganic materials 0.000 claims abstract description 5
150000002367 halogens Chemical class 0.000 claims abstract description 5
-1 nitrogen-containing heterocyclic compounds Chemical class 0.000 claims description 64
150000001875 compounds Chemical class 0.000 claims description 34
239000000203 mixture Substances 0.000 claims description 26
239000000975 dye Substances 0.000 claims description 21
238000004043 dyeing Methods 0.000 claims description 17
150000003839 salts Chemical class 0.000 claims description 17
239000002253 acid Substances 0.000 claims description 16
150000001413 amino acids Chemical class 0.000 claims description 12
239000007800 oxidant agent Substances 0.000 claims description 11
PLIKAWJENQZMHA-UHFFFAOYSA-N 4-aminophenol Chemical compound NC1=CC=C(O)C=C1 PLIKAWJENQZMHA-UHFFFAOYSA-N 0.000 claims description 10
238000004040 coloring Methods 0.000 claims description 10
108010038807 Oligopeptides Proteins 0.000 claims description 9
102000015636 Oligopeptides Human genes 0.000 claims description 9
125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 9
KWSVXCAQFTWTEF-UHFFFAOYSA-N 2-(2,5-diaminophenyl)ethanol Chemical compound NC1=CC=C(N)C(CCO)=C1 KWSVXCAQFTWTEF-UHFFFAOYSA-N 0.000 claims description 8
LUSZGTFNYDARNI-UHFFFAOYSA-N Sesamol Chemical compound OC1=CC=C2OCOC2=C1 LUSZGTFNYDARNI-UHFFFAOYSA-N 0.000 claims description 8
239000000126 substance Substances 0.000 claims description 8
KJCVRFUGPWSIIH-UHFFFAOYSA-N 1-naphthol Chemical compound C1=CC=C2C(O)=CC=CC2=C1 KJCVRFUGPWSIIH-UHFFFAOYSA-N 0.000 claims description 7
OBCSAIDCZQSFQH-UHFFFAOYSA-N 2-methyl-1,4-phenylenediamine Chemical compound CC1=CC(N)=CC=C1N OBCSAIDCZQSFQH-UHFFFAOYSA-N 0.000 claims description 7
PZKNKZNLQYKXFV-UHFFFAOYSA-N 4-amino-2-(aminomethyl)phenol Chemical compound NCC1=CC(N)=CC=C1O PZKNKZNLQYKXFV-UHFFFAOYSA-N 0.000 claims description 7
MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 claims description 7
239000003945 anionic surfactant Substances 0.000 claims description 7
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 7
GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 claims description 7
125000000467 secondary amino group Chemical group [H]N([*:1])[*:2] 0.000 claims description 7
229910052717 sulfur Inorganic materials 0.000 claims description 7
229940075142 2,5-diaminotoluene Drugs 0.000 claims description 6
125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 claims description 6
KFZMGEQAYNKOFK-UHFFFAOYSA-N 2-propanol Substances CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 claims description 6
GHVHDYYKJYXFGU-UHFFFAOYSA-N Beta-Orcinol Chemical compound CC1=CC(O)=C(C)C(O)=C1 GHVHDYYKJYXFGU-UHFFFAOYSA-N 0.000 claims description 6
239000002280 amphoteric surfactant Substances 0.000 claims description 6
OIPPWFOQEKKFEE-UHFFFAOYSA-N orcinol Chemical compound CC1=CC(O)=CC(O)=C1 OIPPWFOQEKKFEE-UHFFFAOYSA-N 0.000 claims description 6
XGNXYCFREOZBOL-UHFFFAOYSA-N 1,3-benzodioxol-5-amine Chemical compound NC1=CC=C2OCOC2=C1 XGNXYCFREOZBOL-UHFFFAOYSA-N 0.000 claims description 5
CBCKQZAAMUWICA-UHFFFAOYSA-N 1,4-phenylenediamine Chemical compound NC1=CC=C(N)C=C1 CBCKQZAAMUWICA-UHFFFAOYSA-N 0.000 claims description 5
ISCYHXYLVTWDJT-UHFFFAOYSA-N 2-[4-amino-n-(2-hydroxyethyl)anilino]ethanol Chemical compound NC1=CC=C(N(CCO)CCO)C=C1 ISCYHXYLVTWDJT-UHFFFAOYSA-N 0.000 claims description 5
ASHGTJPOSUFTGB-UHFFFAOYSA-N 3-methoxyphenol Chemical compound COC1=CC=CC(O)=C1 ASHGTJPOSUFTGB-UHFFFAOYSA-N 0.000 claims description 5
WSEFOZIMAJPJHW-UHFFFAOYSA-N 4-amino-2-(hydroxymethyl)phenol Chemical compound NC1=CC=C(O)C(CO)=C1 WSEFOZIMAJPJHW-UHFFFAOYSA-N 0.000 claims description 5
XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 5
229910052751 metal Chemical class 0.000 claims description 5
239000002184 metal Chemical class 0.000 claims description 5
238000000034 method Methods 0.000 claims description 5
IANQTJSKSUMEQM-UHFFFAOYSA-N 1-benzofuran Chemical compound C1=CC=C2OC=CC2=C1 IANQTJSKSUMEQM-UHFFFAOYSA-N 0.000 claims description 4
KGBBJPZIDRELDP-UHFFFAOYSA-N 1h-pyrazole-3,5-diamine Chemical compound NC=1C=C(N)NN=1 KGBBJPZIDRELDP-UHFFFAOYSA-N 0.000 claims description 4
IBHWREHFNDMRPR-UHFFFAOYSA-N 2,4,6-Trihydroxybenzoic acid Chemical compound OC(=O)C1=C(O)C=C(O)C=C1O IBHWREHFNDMRPR-UHFFFAOYSA-N 0.000 claims description 4
WLJVXDMOQOGPHL-PPJXEINESA-N 2-phenylacetic acid Chemical compound O[14C](=O)CC1=CC=CC=C1 WLJVXDMOQOGPHL-PPJXEINESA-N 0.000 claims description 4
YQUVCSBJEUQKSH-UHFFFAOYSA-N 3,4-dihydroxybenzoic acid Chemical compound OC(=O)C1=CC=C(O)C(O)=C1 YQUVCSBJEUQKSH-UHFFFAOYSA-N 0.000 claims description 4
SGNZYJXNUURYCH-UHFFFAOYSA-N 5,6-dihydroxyindole Chemical compound C1=C(O)C(O)=CC2=C1NC=C2 SGNZYJXNUURYCH-UHFFFAOYSA-N 0.000 claims description 4
QZBGOTVBHYKUDS-UHFFFAOYSA-N 5-amino-1,2-dihydropyrazol-3-one Chemical compound NC1=CC(=O)NN1 QZBGOTVBHYKUDS-UHFFFAOYSA-N 0.000 claims description 4
KIEGFAYDOKCBOK-UHFFFAOYSA-N 6-hydroxy-4,5-dimethyl-1h-pyridin-2-one Chemical compound CC1=CC(=O)NC(O)=C1C KIEGFAYDOKCBOK-UHFFFAOYSA-N 0.000 claims description 4
QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 claims description 4
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims description 4
SIKJAQJRHWYJAI-UHFFFAOYSA-N Indole Chemical compound C1=CC=C2NC=CC2=C1 SIKJAQJRHWYJAI-UHFFFAOYSA-N 0.000 claims description 4
229910052783 alkali metal Inorganic materials 0.000 claims description 4
150000001340 alkali metals Chemical class 0.000 claims description 4
125000000129 anionic group Chemical group 0.000 claims description 4
150000004982 aromatic amines Chemical class 0.000 claims description 4
JSYBAZQQYCNZJE-UHFFFAOYSA-N benzene-1,2,4-triamine Chemical compound NC1=CC=C(N)C(N)=C1 JSYBAZQQYCNZJE-UHFFFAOYSA-N 0.000 claims description 4
GGNQRNBDZQJCCN-UHFFFAOYSA-N benzene-1,2,4-triol Chemical compound OC1=CC=C(O)C(O)=C1 GGNQRNBDZQJCCN-UHFFFAOYSA-N 0.000 claims description 4
VGSVNUGKHOVSPK-UHFFFAOYSA-N leukoaminochrome Chemical compound C1=C(O)C(O)=CC2=C1NCC2 VGSVNUGKHOVSPK-UHFFFAOYSA-N 0.000 claims description 4
239000002736 nonionic surfactant Substances 0.000 claims description 4
150000005619 secondary aliphatic amines Chemical class 0.000 claims description 4
239000011734 sodium Substances 0.000 claims description 4
229910052708 sodium Inorganic materials 0.000 claims description 4
MGLZGLAFFOMWPB-UHFFFAOYSA-N 2-chloro-1,4-phenylenediamine Chemical compound NC1=CC=C(N)C(Cl)=C1 MGLZGLAFFOMWPB-UHFFFAOYSA-N 0.000 claims description 3
RVBUGGBMJDPOST-UHFFFAOYSA-N 2-thiobarbituric acid Chemical compound O=C1CC(=O)NC(=S)N1 RVBUGGBMJDPOST-UHFFFAOYSA-N 0.000 claims description 3
JQVAPEJNIZULEK-UHFFFAOYSA-N 4-chlorobenzene-1,3-diol Chemical compound OC1=CC=C(Cl)C(O)=C1 JQVAPEJNIZULEK-UHFFFAOYSA-N 0.000 claims description 3
QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical class [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 3
229910019142 PO4 Inorganic materials 0.000 claims description 3
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims description 3
QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 claims description 3
HNYOPLTXPVRDBG-UHFFFAOYSA-N barbituric acid Chemical compound O=C1CC(=O)NC(=O)N1 HNYOPLTXPVRDBG-UHFFFAOYSA-N 0.000 claims description 3
150000004649 carbonic acid derivatives Chemical class 0.000 claims description 3
WFSXUTWNNVIIIG-ZPUQHVIOSA-N glutaconaldehyde Chemical compound O\C=C\C=C\C=O WFSXUTWNNVIIIG-ZPUQHVIOSA-N 0.000 claims description 3
150000002476 indolines Chemical class 0.000 claims description 3
229910052757 nitrogen Inorganic materials 0.000 claims description 3
235000021317 phosphate Nutrition 0.000 claims description 3
150000003013 phosphoric acid derivatives Chemical class 0.000 claims description 3
229910052700 potassium Inorganic materials 0.000 claims description 3
239000011591 potassium Substances 0.000 claims description 3
239000002453 shampoo Substances 0.000 claims description 3
VIXBPSTZNCRCJE-UHFFFAOYSA-N 1,3-bis[4-amino-n-(2-hydroxyethyl)anilino]propan-2-ol Chemical compound C1=CC(N)=CC=C1N(CCO)CC(O)CN(CCO)C1=CC=C(N)C=C1 VIXBPSTZNCRCJE-UHFFFAOYSA-N 0.000 claims description 2
KEJFADGISRFLFO-UHFFFAOYSA-N 1H-indazol-6-amine Chemical compound NC1=CC=C2C=NNC2=C1 KEJFADGISRFLFO-UHFFFAOYSA-N 0.000 claims description 2
WTFWZOSMUGZKNZ-UHFFFAOYSA-N 1H-indol-7-amine Chemical compound NC1=CC=CC2=C1NC=C2 WTFWZOSMUGZKNZ-UHFFFAOYSA-N 0.000 claims description 2
NZJKEQFPRPAEPO-UHFFFAOYSA-N 1h-benzimidazol-4-amine Chemical compound NC1=CC=CC2=C1N=CN2 NZJKEQFPRPAEPO-UHFFFAOYSA-N 0.000 claims description 2
OWWAUBQOFLVUMS-UHFFFAOYSA-N 2,3-dihydro-1h-indol-4-ol Chemical compound OC1=CC=CC2=C1CCN2 OWWAUBQOFLVUMS-UHFFFAOYSA-N 0.000 claims description 2
GYHJFWZSCIYJKD-UHFFFAOYSA-M 2,3-dimethyl-1,3-benzothiazol-3-ium;4-methylbenzenesulfonate Chemical compound C1=CC=C2[N+](C)=C(C)SC2=C1.CC1=CC=C(S([O-])(=O)=O)C=C1 GYHJFWZSCIYJKD-UHFFFAOYSA-M 0.000 claims description 2
VZRIFNLQJXPRJI-UHFFFAOYSA-M 2,3-dimethyl-1,3-benzothiazol-3-ium;iodide Chemical compound [I-].C1=CC=C2[N+](C)=C(C)SC2=C1 VZRIFNLQJXPRJI-UHFFFAOYSA-M 0.000 claims description 2
MJMRSGYLARBUDK-UHFFFAOYSA-N 2,4-dimethoxybenzene-1,3-diamine Chemical compound COC1=CC=C(N)C(OC)=C1N MJMRSGYLARBUDK-UHFFFAOYSA-N 0.000 claims description 2
MJXPQLQVKYZJJZ-UHFFFAOYSA-N 2-methyl-5-phenyl-3h-pyrazol-4-one Chemical compound CN1CC(=O)C(C=2C=CC=CC=2)=N1 MJXPQLQVKYZJJZ-UHFFFAOYSA-N 0.000 claims description 2
HEMGYNNCNNODNX-UHFFFAOYSA-N 3,4-diaminobenzoic acid Chemical compound NC1=CC=C(C(O)=O)C=C1N HEMGYNNCNNODNX-UHFFFAOYSA-N 0.000 claims description 2
UENRXLSRMCSUSN-UHFFFAOYSA-N 3,5-diaminobenzoic acid Chemical compound NC1=CC(N)=CC(C(O)=O)=C1 UENRXLSRMCSUSN-UHFFFAOYSA-N 0.000 claims description 2
SHNAFLCZLQETCE-UHFFFAOYSA-N 3-(hydroxymethylidene)cycloheptene-1-carbaldehyde Chemical compound OC=C1CCCCC(C=O)=C1 SHNAFLCZLQETCE-UHFFFAOYSA-N 0.000 claims description 2
FHUXTLJHWSFXCF-UHFFFAOYSA-N 3-(hydroxymethylidene)cyclohexene-1-carbaldehyde Chemical compound OC=C1CCCC(C=O)=C1 FHUXTLJHWSFXCF-UHFFFAOYSA-N 0.000 claims description 2
XFXOLBNQYFRSLQ-UHFFFAOYSA-N 3-amino-2-naphthoic acid Chemical compound C1=CC=C2C=C(C(O)=O)C(N)=CC2=C1 XFXOLBNQYFRSLQ-UHFFFAOYSA-N 0.000 claims description 2
WGLQHUKCXBXUDV-UHFFFAOYSA-N 3-aminophthalic acid Chemical compound NC1=CC=CC(C(O)=O)=C1C(O)=O WGLQHUKCXBXUDV-UHFFFAOYSA-N 0.000 claims description 2
KOGDFDWINXIWHI-OWOJBTEDSA-N 4-[(e)-2-(4-aminophenyl)ethenyl]aniline Chemical compound C1=CC(N)=CC=C1\C=C\C1=CC=C(N)C=C1 KOGDFDWINXIWHI-OWOJBTEDSA-N 0.000 claims description 2
ALYNCZNDIQEVRV-PZFLKRBQSA-N 4-amino-3,5-ditritiobenzoic acid Chemical compound [3H]c1cc(cc([3H])c1N)C(O)=O ALYNCZNDIQEVRV-PZFLKRBQSA-N 0.000 claims description 2
NFPYJDZQOKCYIE-UHFFFAOYSA-N 4-amino-3-hydroxybenzoic acid Chemical compound NC1=CC=C(C(O)=O)C=C1O NFPYJDZQOKCYIE-UHFFFAOYSA-N 0.000 claims description 2
APRRQJCCBSJQOQ-UHFFFAOYSA-N 4-amino-5-hydroxynaphthalene-2,7-disulfonic acid Chemical compound OS(=O)(=O)C1=CC(O)=C2C(N)=CC(S(O)(=O)=O)=CC2=C1 APRRQJCCBSJQOQ-UHFFFAOYSA-N 0.000 claims description 2
SNWZXTZIZWBIDQ-UHFFFAOYSA-N 4-methoxy-6-methylpyrimidin-2-amine Chemical compound COC1=CC(C)=NC(N)=N1 SNWZXTZIZWBIDQ-UHFFFAOYSA-N 0.000 claims description 2
KBZFDRWPMZESDI-UHFFFAOYSA-N 5-aminobenzene-1,3-dicarboxylic acid Chemical compound NC1=CC(C(O)=O)=CC(C(O)=O)=C1 KBZFDRWPMZESDI-UHFFFAOYSA-N 0.000 claims description 2
DTVYNUOOZIKEEX-UHFFFAOYSA-N 5-aminoisoquinoline Chemical compound N1=CC=C2C(N)=CC=CC2=C1 DTVYNUOOZIKEEX-UHFFFAOYSA-N 0.000 claims description 2
LRPIENHBUQIGPP-UHFFFAOYSA-N 6-(dimethylamino)-4-hydroxynaphthalene-2-sulfonic acid Chemical compound C1=C(S(O)(=O)=O)C=C(O)C2=CC(N(C)C)=CC=C21 LRPIENHBUQIGPP-UHFFFAOYSA-N 0.000 claims description 2
MVGYYGCFVPMJAQ-UHFFFAOYSA-N 6-amino-7-hydroxynaphthalene-2-sulfonic acid Chemical compound C1=C(S(O)(=O)=O)C=C2C=C(O)C(N)=CC2=C1 MVGYYGCFVPMJAQ-UHFFFAOYSA-N 0.000 claims description 2
ZCIFWRHIEBXBOY-UHFFFAOYSA-N 6-aminonicotinic acid Chemical compound NC1=CC=C(C(O)=O)C=N1 ZCIFWRHIEBXBOY-UHFFFAOYSA-N 0.000 claims description 2
KYARBIJYVGJZLB-UHFFFAOYSA-N 7-amino-4-hydroxy-2-naphthalenesulfonic acid Chemical compound OC1=CC(S(O)(=O)=O)=CC2=CC(N)=CC=C21 KYARBIJYVGJZLB-UHFFFAOYSA-N 0.000 claims description 2
FVWOTSUMOKOGAM-UHFFFAOYSA-N 7-hydroxyhepta-2,4,6-trienal Chemical compound OC=CC=CC=CC=O FVWOTSUMOKOGAM-UHFFFAOYSA-N 0.000 claims description 2
WREVVZMUNPAPOV-UHFFFAOYSA-N 8-aminoquinoline Chemical compound C1=CN=C2C(N)=CC=CC2=C1 WREVVZMUNPAPOV-UHFFFAOYSA-N 0.000 claims description 2
OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 claims description 2
RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims description 2
OCUCCJIRFHNWBP-IYEMJOQQSA-L Copper gluconate Chemical class [Cu+2].OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C([O-])=O.OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C([O-])=O OCUCCJIRFHNWBP-IYEMJOQQSA-L 0.000 claims description 2
AEMRFAOFKBGASW-UHFFFAOYSA-N Glycolic acid Chemical class OCC(O)=O AEMRFAOFKBGASW-UHFFFAOYSA-N 0.000 claims description 2
WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 claims description 2
FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 claims description 2
PCKPVGOLPKLUHR-UHFFFAOYSA-N OH-Indolxyl Natural products C1=CC=C2C(O)=CNC2=C1 PCKPVGOLPKLUHR-UHFFFAOYSA-N 0.000 claims description 2
ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical class OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 claims description 2
XBDQKXXYIPTUBI-UHFFFAOYSA-N Propionic acid Chemical class CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 claims description 2
UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 claims description 2
150000001242 acetic acid derivatives Chemical class 0.000 claims description 2
229910052784 alkaline earth metal Inorganic materials 0.000 claims description 2
229910052782 aluminium Inorganic materials 0.000 claims description 2
XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 2
150000001412 amines Chemical class 0.000 claims description 2
PYKYMHQGRFAEBM-UHFFFAOYSA-N anthraquinone Natural products CCC(=O)c1c(O)c2C(=O)C3C(C=CC=C3O)C(=O)c2cc1CC(=O)OC PYKYMHQGRFAEBM-UHFFFAOYSA-N 0.000 claims description 2
150000004056 anthraquinones Chemical class 0.000 claims description 2
125000003118 aryl group Chemical group 0.000 claims description 2
239000000987 azo dye Substances 0.000 claims description 2
229910052788 barium Inorganic materials 0.000 claims description 2
DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 claims description 2
OWSZUKMVEBFJMZ-UHFFFAOYSA-N benzene-1,2,3,4,5,6-hexamine Chemical compound NC1=C(N)C(N)=C(N)C(N)=C1N OWSZUKMVEBFJMZ-UHFFFAOYSA-N 0.000 claims description 2
ZLSMCQSGRWNEGX-UHFFFAOYSA-N bis(4-aminophenyl)methanone Chemical compound C1=CC(N)=CC=C1C(=O)C1=CC=C(N)C=C1 ZLSMCQSGRWNEGX-UHFFFAOYSA-N 0.000 claims description 2
150000004648 butanoic acid derivatives Chemical class 0.000 claims description 2
229910052791 calcium Inorganic materials 0.000 claims description 2
239000011575 calcium Substances 0.000 claims description 2
150000001860 citric acid derivatives Chemical class 0.000 claims description 2
229910017052 cobalt Inorganic materials 0.000 claims description 2
239000010941 cobalt Substances 0.000 claims description 2
GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 claims description 2
229910052802 copper Inorganic materials 0.000 claims description 2
239000010949 copper Substances 0.000 claims description 2
239000002537 cosmetic Substances 0.000 claims description 2
150000004820 halides Chemical class 0.000 claims description 2
PZOUSPYUWWUPPK-UHFFFAOYSA-N indole Natural products CC1=CC=CC2=C1C=CN2 PZOUSPYUWWUPPK-UHFFFAOYSA-N 0.000 claims description 2
RKJUIXBNRJVNHR-UHFFFAOYSA-N indolenine Natural products C1=CC=C2CC=NC2=C1 RKJUIXBNRJVNHR-UHFFFAOYSA-N 0.000 claims description 2
JYGFTBXVXVMTGB-UHFFFAOYSA-N indolin-2-one Chemical compound C1=CC=C2NC(=O)CC2=C1 JYGFTBXVXVMTGB-UHFFFAOYSA-N 0.000 claims description 2
RSAZYXZUJROYKR-UHFFFAOYSA-N indophenol Chemical compound C1=CC(O)=CC=C1N=C1C=CC(=O)C=C1 RSAZYXZUJROYKR-UHFFFAOYSA-N 0.000 claims description 2
229910052742 iron Inorganic materials 0.000 claims description 2
150000003893 lactate salts Chemical class 0.000 claims description 2
229910052744 lithium Inorganic materials 0.000 claims description 2
229910052749 magnesium Inorganic materials 0.000 claims description 2
239000011777 magnesium Substances 0.000 claims description 2
WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 claims description 2
KBOPZPXVLCULAV-UHFFFAOYSA-N mesalamine Chemical compound NC1=CC=C(O)C(C(O)=O)=C1 KBOPZPXVLCULAV-UHFFFAOYSA-N 0.000 claims description 2
229960004963 mesalazine Drugs 0.000 claims description 2
150000007522 mineralic acids Chemical class 0.000 claims description 2
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Classifications

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- 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
- 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
- A61K8/4973—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with oxygen as the only hetero atom
- 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

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Health & Medical Sciences (AREA)
Life Sciences & Earth Sciences (AREA)
Animal Behavior & Ethology (AREA)
General Health & Medical Sciences (AREA)
Public Health (AREA)
Veterinary Medicine (AREA)
Birds (AREA)
Epidemiology (AREA)
Emergency Medicine (AREA)
Cosmetics (AREA)

SK1455-99A 1997-04-24 1998-04-16 Use of unsaturated aldehydes in dying fibers containing keratin SK145599A3 (en)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
DE19717224A DE19717224A1 (de)	1997-04-24	1997-04-24	Verwendung von ungesättigten Aldehyden zum Färben von keratinhaltigen Fasern
PCT/EP1998/002243 WO1998047473A1 (de)	1997-04-24	1998-04-16	Verwendung von ungesättigten aldehyden zum färben von keratinhaltigen fasern

Publications (1)

Publication Number	Publication Date
SK145599A3 true SK145599A3 (en)	2000-05-16

Family

ID=7827552

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
SK1455-99A SK145599A3 (en)	1997-04-24	1998-04-16	Use of unsaturated aldehydes in dying fibers containing keratin

Country Status (12)

Country	Link
EP (1)	EP0977546A1 (de)
JP (1)	JP2001524091A (de)
CN (1)	CN1252707A (de)
AU (1)	AU726113B2 (de)
BR (1)	BR9809417A (de)
CA (1)	CA2288055A1 (de)
DE (1)	DE19717224A1 (de)
HU (1)	HUP0002707A3 (de)
NO (1)	NO995157D0 (de)
PL (1)	PL336070A1 (de)
SK (1)	SK145599A3 (de)
WO (1)	WO1998047473A1 (de)

Families Citing this family (25)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE19820894A1 (de) *	1998-05-09	1999-11-11	Wella Ag	Mittel und Verfahren zum Färben von Fasern
ATE258421T1 (de) *	1998-06-23	2004-02-15	Henkel Kgaa	Färbemittel zum färben von keratinfasern
US7214248B1 (en)	1998-12-07	2007-05-08	Wella Ag	Multi-component kit and method for temporarily dyeing and later decolorizing hair
FR2787708B1 (fr) *	1998-12-23	2002-09-13	Oreal	Procede de teinture mettant en oeuvre un compose a methylene actif et un compose choisi parmi un aldehyde, une cetone, une quinone et un derive de la di-imino-isoindoline ou de la 3-amino-isoindolone
FR2787707B1 (fr) *	1998-12-23	2002-09-20	Oreal	Procede de teinture mettant en oeuvre un derive cationique et un compose choisi parmi un aldehyde, une cetone, une quinone et un derive de la di-imino-isoindoline ou de la 3-amino-isoindolone
WO2000052100A1 (de) *	1999-02-27	2000-09-08	Wella Aktiengesellschaft	Mittel zum färben von fasern
DE19916030A1 (de) *	1999-04-09	2000-10-19	Henkel Kgaa	Färbemittel und Verwendung
DE19949033A1 (de) *	1999-10-12	2001-04-19	Henkel Kgaa	Haarfärbeverfahren
DE19950404B4 (de) *	1999-10-20	2004-07-15	Wella Ag	Mittel und Verfahren zur Färbung von Haaren sowie ein Mehrkomponenten-Kit zum Färben und späteren Entfärben von Haaren
DE19951134A1 (de)	1999-10-23	2001-04-26	Henkel Kgaa	Mittel zum Färben von keratinhaltigen Fasern
DE10045856A1 (de)	2000-09-14	2002-03-28	Henkel Kgaa	Haarfärbemittel mit Indigoderivaten
DE10148671A1 (de)	2001-10-02	2003-04-10	Henkel Kgaa	Verfahren zum Färben von Keratinfasern unter Verwendung von Carbonylverbindungen zur Verbesserung der Farbstabilität von Haarfärbungen
ES2435511T3 (es)	2002-01-15	2013-12-20	Basf Se	Colorantes catiónicos de color amarillo para coloración de material orgánico
DE10218588A1 (de)	2002-04-26	2003-11-06	Wella Ag	Mittel zum oxidativen Färben von Keratinfasern
JP3675776B2 (ja) *	2002-05-02	2005-07-27	倉敷紡績株式会社	繊維の発色制御方法
DE10260881A1 (de) *	2002-12-23	2004-07-08	Henkel Kgaa	Mittel zum Färben von keratinhaltigen Fasern
MXPA06011502A (es)	2004-04-08	2006-12-15	Ciba Sc Holding Ag	Tintes de disulfuro, composicion que comprende los mismos y metodo para tenir el pelo.
JP2009507944A (ja)	2005-08-30	2009-02-26	チバホールディングインコーポレーテッド	チオール基を含む染料
BRPI0617339B1 (pt)	2005-10-11	2017-04-04	Ciba Specialty Chemicals Holding Inc	mistura de corantes de sulfeto, composição compreendendo a mesma, e método para tingir fibras contendo queratina
ES2414461T3 (es)	2006-06-13	2013-07-19	Basf Se	Colorantes tricatiónicos
DE102006042075A1 (de) *	2006-09-05	2008-03-06	Henkel Kgaa	Mittel zum Färben von keratinhaltigen Fasern
WO2011006946A2 (en)	2009-07-15	2011-01-20	Basf Se	Polymeric hair dyes
EP2606095B1 (de)	2010-08-17	2016-10-12	Basf Se	Disulfid- oder thiolfunktionalisierte polymere haarfarbstoffe
BR112013028030B1 (pt)	2011-05-03	2021-01-05	Basf Se	composto, método para tingir fibras de queratina humanas, e, composição de tingimento
WO2015059368A1 (fr)	2013-09-02	2015-04-30	L'oreal	Procede de coloration des fibres keratiniques a partir de colorants cationiques styryles disulfures, et composition comprenant lesdits colorants

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
LU49208A1 (de) *	1965-07-29	1967-01-30
US3871818A (en) *	1972-10-30	1975-03-18	Avon Prod Inc	Promoting color change in human hair with a dialdehyde compound and a nitrogen containing compound
DE19501304A1 (de) *	1995-01-18	1996-07-25	Henkel Kgaa	Diketo-Verbindungen zum Färben keratinhaltiger Fasern

1997
- 1997-04-24 DE DE19717224A patent/DE19717224A1/de not_active Withdrawn
1998
- 1998-04-16 SK SK1455-99A patent/SK145599A3/sk unknown
- 1998-04-16 CN CN98804359.9A patent/CN1252707A/zh active Pending
- 1998-04-16 WO PCT/EP1998/002243 patent/WO1998047473A1/de not_active Ceased
- 1998-04-16 AU AU75264/98A patent/AU726113B2/en not_active Ceased
- 1998-04-16 HU HU0002707A patent/HUP0002707A3/hu unknown
- 1998-04-16 PL PL98336070A patent/PL336070A1/xx unknown
- 1998-04-16 JP JP54497798A patent/JP2001524091A/ja active Pending
- 1998-04-16 EP EP98922727A patent/EP0977546A1/de not_active Withdrawn
- 1998-04-16 CA CA002288055A patent/CA2288055A1/en not_active Abandoned
- 1998-04-16 BR BR9809417-3A patent/BR9809417A/pt not_active IP Right Cessation
1999
- 1999-10-22 NO NO995157A patent/NO995157D0/no not_active Application Discontinuation

Also Published As

Publication number	Publication date
HUP0002707A2 (hu)	2000-12-28
NO995157L (no)	1999-10-22
HUP0002707A3 (en)	2002-11-28
EP0977546A1 (de)	2000-02-09
JP2001524091A (ja)	2001-11-27
CA2288055A1 (en)	1998-10-29
NO995157D0 (no)	1999-10-22
CN1252707A (zh)	2000-05-10
DE19717224A1 (de)	1998-10-29
PL336070A1 (en)	2000-06-05
WO1998047473A1 (de)	1998-10-29
BR9809417A (pt)	2000-06-13
AU7526498A (en)	1998-11-13
AU726113B2 (en)	2000-11-02

Publication	Publication Date	Title
ES2232028T3 (es)	2005-05-16	Empleo de aldehidos y de cetonas de onio para el teñido de fibras que contienen queratina.
SK145599A3 (en)	2000-05-16	Use of unsaturated aldehydes in dying fibers containing keratin
WO2000038636A1 (de)	2000-07-06	Mittel zum färben von keratinhaltigen fasern
EP1194117A2 (de)	2002-04-10	Mittel zum färben von keratinhaltigen fasern
WO2000076466A1 (de)	2000-12-21	Xanthenderivate zum färben von keratinhaltigen fasern
EP0977545B1 (de)	2005-02-16	Verwendung von 1-substituierten isatinen zum färben von keratinhaltigen fasern
EP1113779A1 (de)	2001-07-11	Verfahren zum färben von keratinhaltigen fasern unter verwendung von stabilen diazoniumsalzen
WO2000038632A1 (de)	2000-07-06	Verfahren zum färben von keratinhaltigen fasern unter verwendung von 2-oxocarbonsäurederivaten in kombination mit nucleophilen
EP1028694A1 (de)	2000-08-23	Verwendung von indanonen zum färben von keratinhaltigen fasern
EP1139988B1 (de)	2002-09-25	Mittel zum färben von keratinhaltigen fasern
EP0873746A2 (de)	1998-10-28	Mittel zum Färben von keratinhaltigen Fasern
EP1028695A1 (de)	2000-08-23	Mittel zum färben von keratinhaltigen fasern mit einem gehalt an dehydroascorbinsäure
EP1139990B1 (de)	2004-05-06	Mittel zum färben von keratinhaltigen fasern
EP1194116B1 (de)	2005-05-04	Mittel zum färben von keratinhaltigen fasern
WO1999019558A2 (de)	1999-04-22	Verwendung von malonaldehydderivaten zum färben von keratinhaltigen fasern
EP1112055A1 (de)	2001-07-04	Mittel zum färben von keratinhaltigen fasern
DE19859810A1 (de)	2000-06-29	Mittel zum Färben von keratinhaltigen Fasern
WO2001003661A1 (de)	2001-01-18	Mittel zum färben von keratinhaltigen fasern enthaltend mindestens eine aromatische nitrosoverbindung
CZ374099A3 (cs)	2000-04-12	Použití nenasycených aldehydů
WO1999004754A1 (de)	1999-02-04	Verwendung von di- und oligoacylaromaten zum färben von keratinhaltigen fasern