GB793587A - Quaternary ammonium monoazo dye salts and their use - Google Patents
Quaternary ammonium monoazo dye salts and their useInfo
- Publication number
- GB793587A GB793587A GB2739/56A GB273956A GB793587A GB 793587 A GB793587 A GB 793587A GB 2739/56 A GB2739/56 A GB 2739/56A GB 273956 A GB273956 A GB 273956A GB 793587 A GB793587 A GB 793587A
- Authority
- GB
- United Kingdom
- Prior art keywords
- amino
- alkyl
- dyestuffs
- ring
- nitroso
- 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
Links
- 150000003839 salts Chemical class 0.000 title abstract 3
- -1 benzyl alkyl anilines Chemical class 0.000 abstract 7
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical group C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 abstract 4
- CUYKNJBYIJFRCU-UHFFFAOYSA-N 3-aminopyridine Chemical compound NC1=CC=CN=C1 CUYKNJBYIJFRCU-UHFFFAOYSA-N 0.000 abstract 3
- 125000003545 alkoxy group Chemical group 0.000 abstract 3
- 125000000217 alkyl group Chemical group 0.000 abstract 3
- 125000003277 amino group Chemical group 0.000 abstract 3
- 239000000975 dye Substances 0.000 abstract 3
- GCMNJUJAKQGROZ-UHFFFAOYSA-N 1,2-Dihydroquinolin-2-imine Chemical compound C1=CC=CC2=NC(N)=CC=C21 GCMNJUJAKQGROZ-UHFFFAOYSA-N 0.000 abstract 2
- 239000002253 acid Substances 0.000 abstract 2
- 125000004442 acylamino group Chemical group 0.000 abstract 2
- 239000002168 alkylating agent Substances 0.000 abstract 2
- 229940100198 alkylating agent Drugs 0.000 abstract 2
- 230000002152 alkylating effect Effects 0.000 abstract 2
- 150000001450 anions Chemical class 0.000 abstract 2
- 125000003118 aryl group Chemical group 0.000 abstract 2
- 125000000751 azo group Chemical group [*]N=N[*] 0.000 abstract 2
- 238000005859 coupling reaction Methods 0.000 abstract 2
- 125000000623 heterocyclic group Chemical group 0.000 abstract 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 2
- 125000001424 substituent group Chemical group 0.000 abstract 2
- JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 abstract 2
- VSWICNJIUPRZIK-UHFFFAOYSA-N 1,2,3,4-Tetrahydropyridine Natural products C1CNC=CC1 VSWICNJIUPRZIK-UHFFFAOYSA-N 0.000 abstract 1
- ICSNLGPSRYBMBD-UHFFFAOYSA-N 2-aminopyridine Chemical compound NC1=CC=CC=N1 ICSNLGPSRYBMBD-UHFFFAOYSA-N 0.000 abstract 1
- 150000003930 2-aminopyridines Chemical class 0.000 abstract 1
- 150000005013 2-aminoquinolines Chemical class 0.000 abstract 1
- JJYPMNFTHPTTDI-UHFFFAOYSA-N 3-methylaniline Chemical class CC1=CC=CC(N)=C1 JJYPMNFTHPTTDI-UHFFFAOYSA-N 0.000 abstract 1
- OYDRPVHDRYKTLR-UHFFFAOYSA-N 4-(2-piperidin-1-yl-3,4-dihydro-2H-quinolin-1-yl)morpholine Chemical compound N1(CCCCC1)C1N(C2=CC=CC=C2CC1)N1CCOCC1 OYDRPVHDRYKTLR-UHFFFAOYSA-N 0.000 abstract 1
- NUKYPUAOHBNCPY-UHFFFAOYSA-N 4-aminopyridine Chemical compound NC1=CC=NC=C1 NUKYPUAOHBNCPY-UHFFFAOYSA-N 0.000 abstract 1
- ORLGLBZRQYOWNA-UHFFFAOYSA-N 4-methylpyridin-2-amine Chemical compound CC1=CC=NC(N)=C1 ORLGLBZRQYOWNA-UHFFFAOYSA-N 0.000 abstract 1
- QCCKSFHMARIKSK-UHFFFAOYSA-N 5,6-dihydro-4h-pyrrolo[3,2,1-ij]quinoline Chemical compound C1CCC2=CC=CC3=C2N1C=C3 QCCKSFHMARIKSK-UHFFFAOYSA-N 0.000 abstract 1
- QUXLCYFNVNNRBE-UHFFFAOYSA-N 6-methylpyridin-2-amine Chemical compound CC1=CC=CC(N)=N1 QUXLCYFNVNNRBE-UHFFFAOYSA-N 0.000 abstract 1
- JRLTTZUODKEYDH-UHFFFAOYSA-N 8-methylquinoline Chemical group C1=CN=C2C(C)=CC=CC2=C1 JRLTTZUODKEYDH-UHFFFAOYSA-N 0.000 abstract 1
- 229920003043 Cellulose fiber Polymers 0.000 abstract 1
- 208000006558 Dental Calculus Diseases 0.000 abstract 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 abstract 1
- 150000007513 acids Chemical class 0.000 abstract 1
- 150000001298 alcohols Chemical class 0.000 abstract 1
- 125000002723 alicyclic group Chemical group 0.000 abstract 1
- 125000001931 aliphatic group Chemical group 0.000 abstract 1
- 125000003710 aryl alkyl group Chemical group 0.000 abstract 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 1
- 150000001733 carboxylic acid esters Chemical class 0.000 abstract 1
- 150000001735 carboxylic acids Chemical class 0.000 abstract 1
- 150000001768 cations Chemical group 0.000 abstract 1
- 125000004122 cyclic group Chemical group 0.000 abstract 1
- UKJLNMAFNRKWGR-UHFFFAOYSA-N cyclohexatrienamine Chemical group NC1=CC=C=C[CH]1 UKJLNMAFNRKWGR-UHFFFAOYSA-N 0.000 abstract 1
- DENRZWYUOJLTMF-UHFFFAOYSA-N diethyl sulfate Chemical compound CCOS(=O)(=O)OCC DENRZWYUOJLTMF-UHFFFAOYSA-N 0.000 abstract 1
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 abstract 1
- 238000004043 dyeing Methods 0.000 abstract 1
- 239000002895 emetic Substances 0.000 abstract 1
- 150000002148 esters Chemical class 0.000 abstract 1
- 125000004494 ethyl ester group Chemical group 0.000 abstract 1
- 229960004979 fampridine Drugs 0.000 abstract 1
- 229910052736 halogen Inorganic materials 0.000 abstract 1
- 125000005843 halogen group Chemical group 0.000 abstract 1
- 150000002367 halogens Chemical class 0.000 abstract 1
- 229910052500 inorganic mineral Inorganic materials 0.000 abstract 1
- DZFWNZJKBJOGFQ-UHFFFAOYSA-N julolidine Chemical compound C1CCC2=CC=CC3=C2N1CCC3 DZFWNZJKBJOGFQ-UHFFFAOYSA-N 0.000 abstract 1
- 239000010985 leather Substances 0.000 abstract 1
- 239000000463 material Substances 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 239000011707 mineral Substances 0.000 abstract 1
- 235000010755 mineral Nutrition 0.000 abstract 1
- 239000003960 organic solvent Substances 0.000 abstract 1
- 125000005327 perimidinyl group Chemical class N1C(=NC2=CC=CC3=CC=CC1=C23)* 0.000 abstract 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 1
- 125000003884 phenylalkyl group Chemical group 0.000 abstract 1
- 229920002239 polyacrylonitrile Polymers 0.000 abstract 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 abstract 1
- 150000003248 quinolines Chemical class 0.000 abstract 1
- 125000002943 quinolinyl group Chemical group N1=C(C=CC2=CC=CC=C12)* 0.000 abstract 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-N sulfonic acid Chemical compound OS(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-N 0.000 abstract 1
- 235000018553 tannin Nutrition 0.000 abstract 1
- 229920001864 tannin Polymers 0.000 abstract 1
- 239000001648 tannin Substances 0.000 abstract 1
- 125000001302 tertiary amino group Chemical group 0.000 abstract 1
- 239000011592 zinc chloride Substances 0.000 abstract 1
- 235000005074 zinc chloride Nutrition 0.000 abstract 1
Classifications
-
- 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
- C09B27/00—Preparations in which the azo group is formed in any way other than by diazotising and coupling, e.g. oxidation
-
- 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
- C09B44/00—Azo dyes containing onium groups
- C09B44/10—Azo dyes containing onium groups containing cyclammonium groups attached to an azo group by a carbon atom of the ring system
- C09B44/12—Azo dyes containing onium groups containing cyclammonium groups attached to an azo group by a carbon atom of the ring system having one nitrogen atom as the only ring hetero atom
- C09B44/126—Azo dyes containing onium groups containing cyclammonium groups attached to an azo group by a carbon atom of the ring system having one nitrogen atom as the only ring hetero atom in a six-membered ring, e.g. pyrridinium, quinolinium
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH793587X | 1955-01-28 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB793587A true GB793587A (en) | 1958-04-16 |
Family
ID=4537144
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB2739/56A Expired GB793587A (en) | 1955-01-28 | 1956-01-27 | Quaternary ammonium monoazo dye salts and their use |
Country Status (8)
Families Citing this family (29)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE963176C (de) * | 1954-07-05 | 1957-05-02 | Basf Ag | Verfahren zur Herstellung von Azofarbstoffen |
IT555812A (US20100223739A1-20100909-C00025.png) * | 1954-12-15 | |||
US2893816A (en) * | 1957-03-01 | 1959-07-07 | American Cyanamid Co | Polyacrylonitriles dyed with quaternized heterocyclic azo dyes |
US3151106A (en) * | 1958-09-30 | 1964-09-29 | American Cyanamid Co | Pyridinium azo dyes and process for their production |
US3051697A (en) * | 1958-10-06 | 1962-08-28 | American Cyanamid Co | Azomonazone n-oxides, production and deoxygenation |
DE1151612B (de) * | 1959-04-17 | 1963-07-18 | Basf Ag | Verfahren zur Herstellung basischer Farbstoffe |
US3118871A (en) * | 1960-12-12 | 1964-01-21 | American Cyanamid Co | Monazinium azo compounds |
US3312681A (en) * | 1961-11-10 | 1967-04-04 | American Cyanamid Co | Cationic 1-alkyl-3-(2-hydroxy-1-naphthylazo) pyridinium dyes |
US3330617A (en) * | 1961-11-10 | 1967-07-11 | American Cyanamid Co | Polymeric fibers colored with cationic dyestuffs |
US3192195A (en) * | 1962-10-22 | 1965-06-29 | Du Pont | Azostyryl cationic dyes |
LU70835A1 (US20100223739A1-20100909-C00025.png) * | 1974-08-30 | 1976-08-19 | ||
LU71015A1 (US20100223739A1-20100909-C00025.png) * | 1974-09-27 | 1976-08-19 | ||
CH606318A5 (US20100223739A1-20100909-C00025.png) * | 1974-10-29 | 1978-10-31 | Ciba Geigy Ag | |
US4138396A (en) * | 1975-01-03 | 1979-02-06 | Ciba-Geigy Corporation | Pyridyl-azo-indolyl cationic dyes |
CH606300A5 (US20100223739A1-20100909-C00025.png) * | 1975-01-03 | 1978-10-31 | Ciba Geigy Ag | |
US4148642A (en) * | 1978-03-07 | 1979-04-10 | Eastman Kodak Company | Photographic products and processes employing nondiffusible 1-arylazo-4-isoquinolinol dye-releasing compounds |
US4366218A (en) * | 1981-07-13 | 1982-12-28 | Eastman Kodak Company | Photographic products and processes employing novel nondiffusible bridged azdaminophenol magenta dye-releasing compounds and precursors thereof |
US4368249A (en) * | 1981-07-13 | 1983-01-11 | Eastman Kodak Company | Photographic products and processes employing novel nondiffusible pyridylazo(dialkylamino)phenol magenta dye-releasing compounds and precursors thereof |
US4368154A (en) * | 1981-07-13 | 1983-01-11 | Eastman Kodak Company | Photographic products and processes employing novel nondiffusible bridged azoaminophenol magenta dye-releasing compounds and precursors thereof |
US4367174A (en) * | 1981-07-13 | 1983-01-04 | Eastman Kodak Company | Photographic products and processes employing novel nondiffusible pyridylazo(dialkylamino)phenol magenta dye-releasing compounds and precursors thereof |
US4357410A (en) * | 1981-07-13 | 1982-11-02 | Eastman Kodak Company | Photographic products and processes employing novel nondiffusible pyridylazo(dialkylamino) phenol magenta dye-releasing compounds and precursors thereof |
US4368248A (en) * | 1981-07-13 | 1983-01-11 | Eastman Kodak Company | Photographic products and processes employing novel nondiffusible 2-(2-pyridylazo)-4,5-bis(tertiary amino)phenol black dye-releasing compounds and precursors thereof |
US4368153A (en) * | 1981-07-13 | 1983-01-11 | Eastman Kodak Company | Photographic products and processes employing novel nondiffusible 2-(2-pyridylazo)-4,5-bis(tertiary amino)phenol black dye-releasing compounds and precursors thereof |
US4357412A (en) * | 1981-07-13 | 1982-11-02 | Eastman Kodak Company | Photographic products and processes employing novel nondiffusible bridged azoaminophenol magenta dye-releasing compounds and precursors thereof |
US4357411A (en) * | 1981-07-13 | 1982-11-02 | Eastman Kodak Company | Photographic products and processes employing novel nondiffusible 2-(2-pyridylazo)-4,5-bis(tertiary amino)phenol black dye-releasing compounds and precursors thereof |
US4562248A (en) * | 1983-11-25 | 1985-12-31 | Eastman Kodak Company | Azo dyes from unsubstituted or substituted 3-amino-pyridine and aryl or heterocyclic couplers |
FR2920778B1 (fr) * | 2007-09-11 | 2009-10-30 | Oreal | Composes quinoliniums azoiques a motif disulfure/thiol, compositions les comprenant, procede de coloration de fibres keratiniques et dispositif. |
FR2921382B1 (fr) | 2007-09-21 | 2009-10-30 | Oreal | Colorant derive de phenyl-pyridol[1,2-a]indolium thiol-disulfure, composition tinctoriale comprenant ce colorant, procede d'eclaircissement des matieres keratiniques a partir de ce colorant |
FR2921258A1 (fr) * | 2007-09-24 | 2009-03-27 | Oreal | Composition tinctoriale comprenant au moins un precurseur incolore disulfures/thiol, proced de coloration a partir de la composition |
Family Cites Families (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2022921A (en) * | 1931-11-07 | 1935-12-03 | Winthrop Chem Co Inc | Amino azo compound |
DE622596C (de) * | 1932-12-09 | 1935-12-02 | I G Farbenindustrie Akt Ges | Verfahren zur Darstellung basischer Azoverbindungen der Chinolinreihe |
US2135293A (en) * | 1936-08-20 | 1938-11-01 | Pyridium Corp | Medicinal azo dyes |
US2283220A (en) * | 1939-06-02 | 1942-05-19 | Eastman Kodak Co | Azo compounds and material colored therewith |
US2294390A (en) * | 1939-09-29 | 1942-09-01 | Pacific Foundry Company Ltd | Cremator |
US2744105A (en) * | 1952-05-10 | 1956-05-01 | Du Pont | Azonitriles containing quaternary ammonium salt groups |
-
0
- CA CA569011A patent/CA569011A/en not_active Expired
- BE BE544768D patent/BE544768A/xx unknown
- IT IT555459D patent/IT555459A/it unknown
-
1955
- 1955-01-28 CH CH340928D patent/CH340928A/de unknown
-
1956
- 1956-01-23 US US560872A patent/US2864813A/en not_active Expired - Lifetime
- 1956-01-27 GB GB2739/56A patent/GB793587A/en not_active Expired
- 1956-01-27 DE DEG18866A patent/DE1061923B/de active Pending
- 1956-01-27 FR FR1145752D patent/FR1145752A/fr not_active Expired
Also Published As
Publication number | Publication date |
---|---|
FR1145752A (fr) | 1957-10-29 |
BE544768A (US20100223739A1-20100909-C00025.png) | |
DE1061923B (de) | 1959-07-23 |
US2864813A (en) | 1958-12-16 |
IT555459A (US20100223739A1-20100909-C00025.png) | |
CH340928A (de) | 1959-09-15 |
CA569011A (en) | 1959-01-13 |
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