GB1295789A - - Google Patents

Info

Publication number
GB1295789A
GB1295789A GB1295789DA GB1295789A GB 1295789 A GB1295789 A GB 1295789A GB 1295789D A GB1295789D A GB 1295789DA GB 1295789 A GB1295789 A GB 1295789A
Authority
GB
United Kingdom
Prior art keywords
aqueous
formula
indamine
compounds
diaminopyridine
Prior art date
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
Application number
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.)
Filing date
Publication date
Application filed filed Critical
Publication of GB1295789A publication Critical patent/GB1295789A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D213/00Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/60Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D213/72Nitrogen atoms
    • C07D213/74Amino or imino radicals substituted by hydrocarbon or substituted hydrocarbon radicals
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/40Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
    • A61K8/41Amines
    • A61K8/413Indoanilines; Indophenol; Indoamines
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q5/00Preparations for care of the hair
    • A61Q5/10Preparations for permanently dyeing the hair
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06PDYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
    • D06P3/00Special processes of dyeing or printing textiles, or dyeing leather, furs, or solid macromolecular substances in any form, classified according to the material treated
    • D06P3/02Material containing basic nitrogen
    • D06P3/04Material containing basic nitrogen containing amide groups
    • D06P3/08Material containing basic nitrogen containing amide groups using oxidation dyes

Landscapes

  • Health & Medical Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Epidemiology (AREA)
  • Engineering & Computer Science (AREA)
  • Birds (AREA)
  • Textile Engineering (AREA)
  • Cosmetics (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Coloring (AREA)

Abstract

1295789 Indamine dyestuffs L'OREAL 19 April 1971 [10 April 1970] 26659/71. Heading C4P Indamine dyes and their inorganic or organic addition salts have the general formula wherein each of R 1 , R 2 , R 3 and B 4 independently represent H, halogen, C 1 -C 6 alkyl or alkoxy and R 5 and R 6 either both represent hydrogen or both represent the same or different optionally substituted alkyl radicals. Suitable salts include the tartrates, acetates, arylsulphonates, hydrochlorides, persulphates, perchlorates and the zinc chloride double salts. The compounds may be prepared by condensing 2,6-diaminopyridine with a para-phenylene diamine of formula in an aqueous, aqueous alcoholic or aqueous acetone medium in the presence of an oxidizing agent and optionally converting the resulting indamine or indamine salt into a desired salt. The oxidizing agent is suitably H 2 O 2 or an inorganic per-salt. Compounds where at least 2 of R 1 , R 2 , R 3 and R 4 are not hydrogen may be obtained by condensing 2,6-diaminopyridine with a quinone diimine of formula in an aqueous medium or in an inert solvent, in the presence of an acid corresponding to the desired salt. Compounds where R 5 and R 6 are both alkyl groups may also be prepared by condensing 2,6-diaminopyridine with a pnitroso-N,N-dialkylanidine of formula in an aqueous or alcoholic medium at 30-60‹ C. The compounds of Formula I are used for dyeing keratinaceous fibres, e.g. hair, either alone or in compositions containing other dyes and other ingredients conventionally employed in hair dyes. They can also be employed in the form of wave-setting lotions.
GB1295789D 1970-04-10 1971-04-19 Expired GB1295789A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
LU60702 1970-04-10

Publications (1)

Publication Number Publication Date
GB1295789A true GB1295789A (en) 1972-11-08

Family

ID=19726324

Family Applications (1)

Application Number Title Priority Date Filing Date
GB1295789D Expired GB1295789A (en) 1970-04-10 1971-04-19

Country Status (15)

Country Link
AT (1) AT316017B (en)
BE (1) BE765548A (en)
BR (1) BR7102076D0 (en)
CA (1) CA976961A (en)
CH (1) CH536112A (en)
DE (1) DE2117363A1 (en)
DK (1) DK131543C (en)
ES (1) ES390037A1 (en)
FR (1) FR2089423A5 (en)
GB (1) GB1295789A (en)
IT (1) IT1036041B (en)
LU (1) LU60702A1 (en)
NL (1) NL7104666A (en)
SE (1) SE378252B (en)
SU (1) SU440834A3 (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE4031722A1 (en) * 1990-10-06 1992-04-09 Basf Ag PYRIDONE DYES AND A METHOD FOR THEIR THERMAL TRANSFER
FR2845387B1 (en) * 2002-10-04 2005-01-21 Oreal NEW HETEROAROMATIC TRINOCAL BLACK DIRECT COLORANTS

Also Published As

Publication number Publication date
CH536112A (en) 1973-04-30
DK131543B (en) 1975-08-04
BR7102076D0 (en) 1973-05-10
IT1036041B (en) 1979-10-30
DE2117363A1 (en) 1971-10-28
CA976961A (en) 1975-10-28
NL7104666A (en) 1971-10-12
DK131543C (en) 1976-02-02
AT316017B (en) 1974-06-25
LU60702A1 (en) 1972-02-10
BE765548A (en) 1971-10-11
SE378252B (en) 1975-08-25
ES390037A1 (en) 1973-06-01
SU440834A3 (en) 1974-08-25
FR2089423A5 (en) 1972-01-07

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Legal Events

Date Code Title Description
PS Patent sealed [section 19, patents act 1949]
PCNP Patent ceased through non-payment of renewal fee