NO116772B - - Google Patents

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Info

Publication number: NO116772B
Authority: NO; Norway
Prior art keywords: weight; parts; hair; dyes; cream
Prior art date: 1963-09-04

Application number

NO154628A

Other languages

English (en)

Norwegian (no)

Inventor

K Boosen

G Reese

Original Assignee

Therachemie Chem Therapeut

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.)

1963-09-04

Filing date

1964-09-03

Publication date

1969-05-19

1963-09-04 Priority claimed from DE1963T0024643 external-priority patent/DE1248865C2/de

1964-09-03 Application filed by Therachemie Chem Therapeut filed Critical Therachemie Chem Therapeut

1969-05-19 Publication of NO116772B publication Critical patent/NO116772B/no

Links

239000000975 dye Substances 0.000 claims description 21
239000006071 cream Substances 0.000 claims description 13
239000000118 hair dye Substances 0.000 claims description 11
239000003599 detergent Substances 0.000 claims description 7
KHUFHLFHOQVFGB-UHFFFAOYSA-N 1-aminoanthracene-9,10-dione Chemical compound O=C1C2=CC=CC=C2C(=O)C2=C1C=CC=C2N KHUFHLFHOQVFGB-UHFFFAOYSA-N 0.000 claims description 5
RZVHIXYEVGDQDX-UHFFFAOYSA-N 9,10-anthraquinone Chemical group C1=CC=C2C(=O)C3=CC=CC=C3C(=O)C2=C1 RZVHIXYEVGDQDX-UHFFFAOYSA-N 0.000 claims description 3
239000000080 wetting agent Substances 0.000 claims description 3
MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 claims description 2
125000001183 hydrocarbyl group Chemical group 0.000 claims description 2
229910052757 nitrogen Inorganic materials 0.000 claims description 2
125000004433 nitrogen atom Chemical group N* 0.000 claims description 2
229910052760 oxygen Inorganic materials 0.000 claims description 2
239000001301 oxygen Substances 0.000 claims description 2
210000004209 hair Anatomy 0.000 description 20
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 15
-1 amino, hydroxyl Chemical group 0.000 description 6
150000001875 compounds Chemical class 0.000 description 6
239000003795 chemical substances by application Substances 0.000 description 5
QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 4
238000001035 drying Methods 0.000 description 4
150000002191 fatty alcohols Chemical class 0.000 description 4
239000000843 powder Substances 0.000 description 4
SDICTISQCKLMEB-UHFFFAOYSA-N 1,4-diamino-5-nitroanthracene-9,10-dione Chemical compound O=C1C=2C(N)=CC=C(N)C=2C(=O)C2=C1C=CC=C2[N+]([O-])=O SDICTISQCKLMEB-UHFFFAOYSA-N 0.000 description 3
BXGYBSJAZFGIPX-UHFFFAOYSA-N 2-pyridin-2-ylethanol Chemical compound OCCC1=CC=CC=N1 BXGYBSJAZFGIPX-UHFFFAOYSA-N 0.000 description 3
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 3
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 3
230000002378 acidificating effect Effects 0.000 description 3
239000000654 additive Substances 0.000 description 3
239000001000 anthraquinone dye Substances 0.000 description 3
229960002887 deanol Drugs 0.000 description 3
235000014113 dietary fatty acids Nutrition 0.000 description 3
238000004043 dyeing Methods 0.000 description 3
239000000194 fatty acid Substances 0.000 description 3
229930195729 fatty acid Natural products 0.000 description 3
238000010438 heat treatment Methods 0.000 description 3
239000000203 mixture Substances 0.000 description 3
239000002453 shampoo Substances 0.000 description 3
239000002904 solvent Substances 0.000 description 3
238000003756 stirring Methods 0.000 description 3
238000005406 washing Methods 0.000 description 3
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 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
NNXSVNHFDAUPRN-UHFFFAOYSA-N 1,4-diamino-2-chloroanthracene-9,10-dione Chemical compound O=C1C2=CC=CC=C2C(=O)C2=C1C(N)=C(Cl)C=C2N NNXSVNHFDAUPRN-UHFFFAOYSA-N 0.000 description 2
PMNLUUOXGOOLSP-UHFFFAOYSA-N 2-mercaptopropanoic acid Chemical compound CC(S)C(O)=O PMNLUUOXGOOLSP-UHFFFAOYSA-N 0.000 description 2
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
LFQSCWFLJHTTHZ-UHFFFAOYSA-N EtOH Substances CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
UEEJHVSXFDXPFK-UHFFFAOYSA-N N-dimethylaminoethanol Chemical compound CN(C)CCO UEEJHVSXFDXPFK-UHFFFAOYSA-N 0.000 description 2
229910021529 ammonia Inorganic materials 0.000 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 description 2
150000004056 anthraquinones Chemical class 0.000 description 2
125000003178 carboxy group Chemical group [H]OC(*)=O 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
239000003086 colorant Substances 0.000 description 2
150000004665 fatty acids Chemical class 0.000 description 2
125000005843 halogen group Chemical group 0.000 description 2
125000005842 heteroatom Chemical group 0.000 description 2
125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
238000002844 melting Methods 0.000 description 2
230000008018 melting Effects 0.000 description 2
230000003020 moisturizing effect Effects 0.000 description 2
GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 description 2
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 description 2
239000000047 product Substances 0.000 description 2
TXQWFIVRZNOPCK-UHFFFAOYSA-N pyridin-4-ylmethanamine Chemical compound NCC1=CC=NC=C1 TXQWFIVRZNOPCK-UHFFFAOYSA-N 0.000 description 2
239000000243 solution Substances 0.000 description 2
125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 description 2
229910021653 sulphate ion Inorganic materials 0.000 description 2
239000002562 thickening agent Substances 0.000 description 2
CWERGRDVMFNCDR-UHFFFAOYSA-N thioglycolic acid Chemical compound OC(=O)CS CWERGRDVMFNCDR-UHFFFAOYSA-N 0.000 description 2
FBMQNRKSAWNXBT-UHFFFAOYSA-N 1,4-diaminoanthracene-9,10-dione Chemical compound O=C1C2=CC=CC=C2C(=O)C2=C1C(N)=CC=C2N FBMQNRKSAWNXBT-UHFFFAOYSA-N 0.000 description 1
GBAXGHVGQJHFQL-UHFFFAOYSA-N 1-(2-hydroxyethylamino)propan-2-ol Chemical compound CC(O)CNCCO GBAXGHVGQJHFQL-UHFFFAOYSA-N 0.000 description 1
AGDJYJUPTJISCC-UHFFFAOYSA-N 1-sulfanylbutane-1-sulfonic acid Chemical compound CCCC(S)S(O)(=O)=O AGDJYJUPTJISCC-UHFFFAOYSA-N 0.000 description 1
VILCJCGEZXAXTO-UHFFFAOYSA-N 2,2,2-tetramine Chemical compound NCCNCCNCCN VILCJCGEZXAXTO-UHFFFAOYSA-N 0.000 description 1
NJWIMFZLESWFIM-UHFFFAOYSA-N 2-(chloromethyl)pyridine Chemical compound ClCC1=CC=CC=N1 NJWIMFZLESWFIM-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
RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 description 1
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
239000005662 Paraffin oil Substances 0.000 description 1
229920002472 Starch Polymers 0.000 description 1
QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
125000001931 aliphatic group Chemical group 0.000 description 1
125000000129 anionic group Chemical group 0.000 description 1
239000001045 blue dye Substances 0.000 description 1
239000004202 carbamide Substances 0.000 description 1
235000012000 cholesterol Nutrition 0.000 description 1
238000004040 coloring Methods 0.000 description 1
239000012043 crude product Substances 0.000 description 1
238000007865 diluting Methods 0.000 description 1
238000010790 dilution Methods 0.000 description 1
239000012895 dilution Substances 0.000 description 1
230000000694 effects Effects 0.000 description 1
230000001804 emulsifying effect Effects 0.000 description 1
239000000284 extract Substances 0.000 description 1
229910052736 halogen Inorganic materials 0.000 description 1
150000002367 halogens Chemical class 0.000 description 1
239000005457 ice water Substances 0.000 description 1
238000011835 investigation Methods 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
238000000034 method Methods 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
GOQYKNQRPGWPLP-UHFFFAOYSA-N n-heptadecyl alcohol Natural products CCCCCCCCCCCCCCCCCO GOQYKNQRPGWPLP-UHFFFAOYSA-N 0.000 description 1
125000000449 nitro group Chemical group [O-][N+](*)=O 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
SUVIGLJNEAMWEG-UHFFFAOYSA-N propane-1-thiol Chemical compound CCCS SUVIGLJNEAMWEG-UHFFFAOYSA-N 0.000 description 1
SHNUBALDGXWUJI-UHFFFAOYSA-N pyridin-2-ylmethanol Chemical compound OCC1=CC=CC=N1 SHNUBALDGXWUJI-UHFFFAOYSA-N 0.000 description 1
239000011541 reaction mixture Substances 0.000 description 1
239000001044 red dye Substances 0.000 description 1
239000008107 starch Substances 0.000 description 1
235000019698 starch Nutrition 0.000 description 1
239000000126 substance Substances 0.000 description 1
125000001424 substituent group Chemical group 0.000 description 1
125000003396 thiol group Chemical group [H]S* 0.000 description 1
238000011282 treatment Methods 0.000 description 1
229940099259 vaseline Drugs 0.000 description 1
239000000052 vinegar Substances 0.000 description 1
235000021419 vinegar Nutrition 0.000 description 1
210000002268 wool Anatomy 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
- A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
- A61K8/35—Ketones, e.g. benzophenone
- A61K8/355—Quinones
- 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
- 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
- C09B1/00—Dyes with anthracene nucleus not condensed with any other ring
- C09B1/16—Amino-anthraquinones
- C09B1/20—Preparation from starting materials already containing the anthracene nucleus
- C09B1/22—Dyes with unsubstituted amino groups
- 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
- C09B1/00—Dyes with anthracene nucleus not condensed with any other ring
- C09B1/16—Amino-anthraquinones
- C09B1/20—Preparation from starting materials already containing the anthracene nucleus
- C09B1/26—Dyes with amino groups substituted by hydrocarbon radicals
- C09B1/264—Dyes with amino groups substituted by hydrocarbon radicals sulfonated
- C09B1/268—Dyes with amino groups substituted by hydrocarbon radicals sulfonated only sulfonated in a substituent
- 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
- C09B1/00—Dyes with anthracene nucleus not condensed with any other ring
- C09B1/16—Amino-anthraquinones
- C09B1/20—Preparation from starting materials already containing the anthracene nucleus
- C09B1/26—Dyes with amino groups substituted by hydrocarbon radicals
- C09B1/28—Dyes with amino groups substituted by hydrocarbon radicals substituted by alkyl, aralkyl or cyclo alkyl groups
- 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
- C09B1/00—Dyes with anthracene nucleus not condensed with any other ring
- C09B1/16—Amino-anthraquinones
- C09B1/20—Preparation from starting materials already containing the anthracene nucleus
- C09B1/26—Dyes with amino groups substituted by hydrocarbon radicals
- C09B1/32—Dyes with amino groups substituted by hydrocarbon radicals substituted by aryl groups
- 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
- C09B1/00—Dyes with anthracene nucleus not condensed with any other ring
- C09B1/50—Amino-hydroxy-anthraquinones; Ethers and esters thereof
- C09B1/54—Amino-hydroxy-anthraquinones; Ethers and esters thereof etherified
- C09B1/545—Anthraquinones with aliphatic, cycloaliphatic or araliphatic ether groups
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06P—DYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
- D06P3/00—Special processes of dyeing or printing textiles, or dyeing leather, furs, or solid macromolecular substances in any form, classified according to the material treated
- D06P3/02—Material containing basic nitrogen
- D06P3/04—Material containing basic nitrogen containing amide groups
- D06P3/30—Material containing basic nitrogen containing amide groups furs feathers, dead hair, furskins, pelts

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Health & Medical Sciences (AREA)
Life Sciences & Earth Sciences (AREA)
Animal Behavior & Ethology (AREA)
General Health & Medical Sciences (AREA)
Public Health (AREA)
Veterinary Medicine (AREA)
Engineering & Computer Science (AREA)
Textile Engineering (AREA)
Emergency Medicine (AREA)
Birds (AREA)
Epidemiology (AREA)
Cosmetics (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

NO154628A 1963-09-04 1964-09-03 NO116772B (da)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
DET24640A DE1203915B (de)	1963-09-04	1963-09-04	Haarfaerbemittel
DE1963T0024643 DE1248865C2 (de)	1963-09-04	1963-09-04	Mittel zum faerben von haaren

Publications (1)

Publication Number	Publication Date
NO116772B true NO116772B (da)	1969-05-19

Family

ID=25999757

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NO154628A NO116772B (da)	1963-09-04	1964-09-03

Country Status (11)

Country	Link
US (2)	US3401003A (da)
BE (1)	BE652619A (da)
CH (1)	CH486245A (da)
DE (1)	DE1203915B (da)
DK (1)	DK112755B (da)
FI (2)	FI42859B (da)
GB (2)	GB1005913A (da)
LU (1)	LU46884A1 (da)
NL (2)	NL144831B (da)
NO (1)	NO116772B (da)
SE (2)	SE320766B (da)

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
GB1050863A (da) *	1964-02-05
US4051155A (en) *	1975-12-15	1977-09-27	Allied Chemical Corporation	Anthraquinone dyes
SE7609628L (sv) *	1976-08-31	1978-03-01	Danielsson Karl Victor	Komposition for fergning av har
US5112359A (en) *	1990-06-04	1992-05-12	Clairol, Inc.	Hair colorants
US5169403A (en) *	1991-11-01	1992-12-08	Clairol, Inc.	Direct dyes having a quaternary center with a long aliphatic chain
US5961664A (en) *	1997-07-10	1999-10-05	Bristol-Myers Squibb Company	Direct hair dye compositions and methods containing novel anthraquinone mixtures
EP1820826A1 (en) *	2006-02-09	2007-08-22	DyStar Textilfarben GmbH & Co. Deutschland KG	Dyestuffs and Hair Dye Compositions

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US2730534A (en) *	1952-12-31	1956-01-10	Gen Aniline & Film Corp	Anthraquinone dyestuffs
DE1150652B (de) *	1955-08-30	1963-06-27	Bayer Ag	Faerben von Polyacrylnitrilfasern
BE553139A (da) *	1955-12-10
US3232934A (en) *	1959-06-25	1966-02-01	Allied Chem	Omega-(1-amino-5 and 8-anthraquinonylamino)-1-ammonium alkanes of 2 to 3 carbon atoms
US3123605A (en) *	1960-01-08	1964-03-03		Basic anthraquinone dyestuffs
US3125586A (en) *	1960-01-08	1964-03-17		Quaternary ammonium salts of z-amino-
NL275142A (da) *	1961-02-23
US3168441A (en) *	1961-07-31	1965-02-02	Clairol Inc	Blue anthraquinone dye
US3253876A (en) *	1963-04-12	1966-05-31	Eastman Kodak Co	Textile dyeing using disazo dyes

1963
- 1963-09-04 DE DET24640A patent/DE1203915B/de active Pending
1964
- 1964-07-13 NL NL646407966A patent/NL144831B/xx not_active IP Right Cessation
- 1964-08-27 US US392607A patent/US3401003A/en not_active Expired - Lifetime
- 1964-08-27 US US392586A patent/US3368942A/en not_active Expired - Lifetime
- 1964-09-02 GB GB35859/64A patent/GB1005913A/en not_active Expired
- 1964-09-02 GB GB35863/64A patent/GB1005915A/en not_active Expired
- 1964-09-03 NL NL6410275A patent/NL6410275A/xx unknown
- 1964-09-03 NO NO154628A patent/NO116772B/no unknown
- 1964-09-03 BE BE652619D patent/BE652619A/xx unknown
- 1964-09-03 DK DK434864AA patent/DK112755B/da unknown
- 1964-09-04 CH CH1157864A patent/CH486245A/de not_active IP Right Cessation
- 1964-09-04 LU LU46884D patent/LU46884A1/xx unknown
- 1964-09-04 SE SE10635/64A patent/SE320766B/xx unknown
- 1964-09-04 FI FI1882/64A patent/FI42859B/fi active
- 1964-09-04 FI FI1883/64A patent/FI42989B/fi active
- 1964-09-04 SE SE10636/64A patent/SE324429B/xx unknown

Also Published As

Publication number	Publication date
LU46884A1 (da)	1965-03-04
NL6407966A (da)	1965-03-05
FI42859B (da)	1970-08-03
US3401003A (en)	1968-09-10
NL144831B (nl)	1975-02-17
SE320766B (da)	1970-02-16
SE324429B (da)	1970-06-01
GB1005913A (en)	1965-09-29
FI42989B (da)	1970-09-02
NL6410275A (da)	1965-03-05
GB1005915A (en)	1965-09-29
BE652619A (da)	1965-03-03
DK112755B (da)	1969-01-13
US3368942A (en)	1968-02-13
CH486245A (de)	1970-02-28
DE1203915B (de)	1965-10-28

Publication	Publication Date	Title
US4840639A (en)	1989-06-20	Agent for dyeing hair
JP3281386B2 (ja)	2002-05-13	ケラチン含有繊維を染色するための方法
US3665036A (en)	1972-05-23	Dye forming nitroparaphenylenediamine sulfonyl derivatives
US4311478A (en)	1982-01-19	Paraphenylenediamines substituted at position 2 of the benzene ring
DE2543100A1 (de)	1976-04-15	Derivate des 3-aminopyridins und sie enthaltende faerbemittel
CH628670A5 (de)	1982-03-15	Verfahren zur herstellung von reaktivfarbstoffen.
NO154629B (no)	1986-08-11	Dispenser for foliemateriale.
US3694138A (en)	1972-09-26	Dyeing human hair with n,n-diaryl alkylenediamine oxidation dye compositions
EP0137178B1 (en)	1990-05-23	Colouring shampoo
US4575378A (en)	1986-03-11	Substituted 4-amino-3-nitrophenols, processes for their preparation and hair-coloring agents containing these compounds
NO116772B (da)	1969-05-19
US4010200A (en)	1977-03-01	N,N-diaryl alkylenediamine oxidation dye compounds
NO172673B (no)	1993-05-18	Preparat for permanent forandring av fargen paa haar og anvendelse derav i et haarblekingspreparat
US2733186A (en)	1956-01-31	Compositions for the dyeing of hair
DE10045599B4 (de)	2004-06-03	Haarfärbemittel auf der Basis von 4-Nitro-2,1,3-benzoxadiazol-Derivaten und dessen Verwendung als Farbstoff zum Färben von Haaren
NO141072B (no)	1979-10-01	Fremgangsmaate til samtidig farging og kondisjonering av haar, og haarfargingspreparat til utfoerelse av fremgangsmaaten
US3697215A (en)	1972-10-10	Dyeing hair with n-(ureidoalkyl)- and n-(thioureidoalkyl) - para - phenylene diamines
US3528972A (en)	1970-09-15	Quaternary anthraquinone morpholino and piperidino salts
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