GB851861A - Improvements relating to heavy metal-containing azo dyestuffs and their use - Google Patents
Improvements relating to heavy metal-containing azo dyestuffs and their useInfo
- Publication number
- GB851861A GB851861A GB2739/57A GB273957A GB851861A GB 851861 A GB851861 A GB 851861A GB 2739/57 A GB2739/57 A GB 2739/57A GB 273957 A GB273957 A GB 273957A GB 851861 A GB851861 A GB 851861A
- Authority
- GB
- United Kingdom
- Prior art keywords
- dyestuffs
- amino
- naphthol
- nitro
- azo
- 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
- 229910001385 heavy metal Inorganic materials 0.000 title abstract 4
- JWAZRIHNYRIHIV-UHFFFAOYSA-N 2-naphthol Chemical compound C1=CC=CC2=CC(O)=CC=C21 JWAZRIHNYRIHIV-UHFFFAOYSA-N 0.000 abstract 10
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 abstract 6
- 125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 abstract 6
- 239000000975 dye Substances 0.000 abstract 6
- 229950011260 betanaphthol Drugs 0.000 abstract 5
- 230000008878 coupling Effects 0.000 abstract 5
- 238000010168 coupling process Methods 0.000 abstract 5
- 238000005859 coupling reaction Methods 0.000 abstract 5
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 5
- ZRHUHDUEXWHZMA-UHFFFAOYSA-N 1,4-dihydropyrazol-5-one Chemical class O=C1CC=NN1 ZRHUHDUEXWHZMA-UHFFFAOYSA-N 0.000 abstract 3
- -1 sulphonyl substituent Chemical group 0.000 abstract 3
- VLZVIIYRNMWPSN-UHFFFAOYSA-N 2-Amino-4-nitrophenol Chemical compound NC1=CC([N+]([O-])=O)=CC=C1O VLZVIIYRNMWPSN-UHFFFAOYSA-N 0.000 abstract 2
- DOPJTDJKZNWLRB-UHFFFAOYSA-N 2-Amino-5-nitrophenol Chemical compound NC1=CC=C([N+]([O-])=O)C=C1O DOPJTDJKZNWLRB-UHFFFAOYSA-N 0.000 abstract 2
- CDAWCLOXVUBKRW-UHFFFAOYSA-N 2-aminophenol Chemical compound NC1=CC=CC=C1O CDAWCLOXVUBKRW-UHFFFAOYSA-N 0.000 abstract 2
- YCOXTKKNXUZSKD-UHFFFAOYSA-N 3,4-xylenol Chemical compound CC1=CC=C(O)C=C1C YCOXTKKNXUZSKD-UHFFFAOYSA-N 0.000 abstract 2
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Natural products CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 abstract 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 abstract 2
- 239000002253 acid Substances 0.000 abstract 2
- RWZYAGGXGHYGMB-UHFFFAOYSA-N anthranilic acid Chemical compound NC1=CC=CC=C1C(O)=O RWZYAGGXGHYGMB-UHFFFAOYSA-N 0.000 abstract 2
- 239000003795 chemical substances by application Substances 0.000 abstract 2
- 229910052736 halogen Inorganic materials 0.000 abstract 2
- 229910052751 metal Inorganic materials 0.000 abstract 2
- 239000002184 metal Substances 0.000 abstract 2
- 238000001465 metallisation Methods 0.000 abstract 2
- NYGZLYXAPMMJTE-UHFFFAOYSA-M metanil yellow Chemical group [Na+].[O-]S(=O)(=O)C1=CC=CC(N=NC=2C=CC(NC=3C=CC=CC=3)=CC=2)=C1 NYGZLYXAPMMJTE-UHFFFAOYSA-M 0.000 abstract 2
- 238000000034 method Methods 0.000 abstract 2
- 150000002790 naphthalenes Chemical class 0.000 abstract 2
- AWMLROSUUNZXQP-UHFFFAOYSA-N 2-amino-4-phenyldiazenylphenol Chemical compound C1=C(O)C(N)=CC(N=NC=2C=CC=CC=2)=C1 AWMLROSUUNZXQP-UHFFFAOYSA-N 0.000 abstract 1
- GRGSHONWRKRWGP-UHFFFAOYSA-N 2-amino-4-sulfobenzoic acid Chemical compound NC1=CC(S(O)(=O)=O)=CC=C1C(O)=O GRGSHONWRKRWGP-UHFFFAOYSA-N 0.000 abstract 1
- QPKNFEVLZVJGBM-UHFFFAOYSA-N 2-aminonaphthalen-1-ol Chemical class C1=CC=CC2=C(O)C(N)=CC=C21 QPKNFEVLZVJGBM-UHFFFAOYSA-N 0.000 abstract 1
- GVBHRNIWBGTNQA-UHFFFAOYSA-N 2-methoxy-4-nitroaniline Chemical compound COC1=CC([N+]([O-])=O)=CC=C1N GVBHRNIWBGTNQA-UHFFFAOYSA-N 0.000 abstract 1
- JBIJLHTVPXGSAM-UHFFFAOYSA-N 2-naphthylamine Chemical compound C1=CC=CC2=CC(N)=CC=C21 JBIJLHTVPXGSAM-UHFFFAOYSA-N 0.000 abstract 1
- DHXPRBHRJQAXHK-UHFFFAOYSA-N 4-amino-3-hydroxy-7-nitronaphthalene-1-sulfonic acid Chemical compound [O-][N+](=O)C1=CC=C2C(N)=C(O)C=C(S(O)(=O)=O)C2=C1 DHXPRBHRJQAXHK-UHFFFAOYSA-N 0.000 abstract 1
- HDHQZCHIXUUSMK-UHFFFAOYSA-N 4-hydroxy-2-quinolone Chemical class C1=CC=C2C(O)=CC(=O)NC2=C1 HDHQZCHIXUUSMK-UHFFFAOYSA-N 0.000 abstract 1
- QYFYIOWLBSPSDM-UHFFFAOYSA-N 6-aminonaphthalen-1-ol Chemical compound OC1=CC=CC2=CC(N)=CC=C21 QYFYIOWLBSPSDM-UHFFFAOYSA-N 0.000 abstract 1
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 abstract 1
- ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 abstract 1
- 125000002252 acyl group Chemical group 0.000 abstract 1
- 125000004442 acylamino group Chemical group 0.000 abstract 1
- 125000003545 alkoxy group Chemical group 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- 125000004390 alkyl sulfonyl group Chemical group 0.000 abstract 1
- 239000007864 aqueous solution Substances 0.000 abstract 1
- 125000004391 aryl sulfonyl group Chemical group 0.000 abstract 1
- 150000001735 carboxylic acids Chemical class 0.000 abstract 1
- 239000005018 casein Substances 0.000 abstract 1
- BECPQYXYKAMYBN-UHFFFAOYSA-N casein, tech. Chemical compound NCCCCC(C(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(CC(C)C)N=C(O)C(CCC(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(C(C)O)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(COP(O)(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(N)CC1=CC=CC=C1 BECPQYXYKAMYBN-UHFFFAOYSA-N 0.000 abstract 1
- 235000021240 caseins Nutrition 0.000 abstract 1
- 229910052804 chromium Inorganic materials 0.000 abstract 1
- 239000011651 chromium Substances 0.000 abstract 1
- 229910017052 cobalt Inorganic materials 0.000 abstract 1
- 239000010941 cobalt Substances 0.000 abstract 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 238000004043 dyeing Methods 0.000 abstract 1
- QELUYTUMUWHWMC-UHFFFAOYSA-N edaravone Chemical compound O=C1CC(C)=NN1C1=CC=CC=C1 QELUYTUMUWHWMC-UHFFFAOYSA-N 0.000 abstract 1
- 150000002367 halogens Chemical class 0.000 abstract 1
- 229910052500 inorganic mineral Inorganic materials 0.000 abstract 1
- 239000004922 lacquer Substances 0.000 abstract 1
- 239000010985 leather Substances 0.000 abstract 1
- 150000002739 metals Chemical class 0.000 abstract 1
- 239000011707 mineral Substances 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 150000004780 naphthols Chemical class 0.000 abstract 1
- 230000007935 neutral effect Effects 0.000 abstract 1
- 229910052759 nickel Inorganic materials 0.000 abstract 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 1
- 150000002989 phenols Chemical class 0.000 abstract 1
- 229920001184 polypeptide Polymers 0.000 abstract 1
- 102000004196 processed proteins & peptides Human genes 0.000 abstract 1
- 108090000765 processed proteins & peptides Proteins 0.000 abstract 1
- 238000009987 spinning Methods 0.000 abstract 1
- 125000001424 substituent group Chemical group 0.000 abstract 1
- FDDDEECHVMSUSB-UHFFFAOYSA-N sulfanilamide Chemical compound NC1=CC=C(S(N)(=O)=O)C=C1 FDDDEECHVMSUSB-UHFFFAOYSA-N 0.000 abstract 1
- DIORMHZUUKOISG-UHFFFAOYSA-N sulfoformic acid Chemical compound OC(=O)S(O)(=O)=O DIORMHZUUKOISG-UHFFFAOYSA-N 0.000 abstract 1
- 229940124530 sulfonamide Drugs 0.000 abstract 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-N sulfonic acid Chemical group OS(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-N 0.000 abstract 1
- 239000004753 textile Substances 0.000 abstract 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 1
- 210000002268 wool Anatomy 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
- C09B45/00—Complex metal compounds of azo dyes
- C09B45/48—Preparation from other complex metal compounds of azo dyes
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Abstract
The invention comprises dyestuffs of formula D1-M-D2 where M is a co-ordinative hexavalent heavy metal atom and D1 and D2 are coordinated mono- and dis-azo dyestuffs respectively. The dyestuffs are made by adding, in a weakly acid, neutral to alkaline medium, a dicyclically metallising azo dyestuff to a dicyclically co-ordinated azo dyestuff which contains a co-ordinative hexavalent heavy metal atom, the dyestuffs being chosen so that the product contains both a mono- and a disazo dyestuff bound at the heavy metal atom. They may also be made by metallising appropriate mixtures of monoand dis-azo dyestuffs. Water-soluble textile dyestuffs are obtained if at least one of the dyestuffs contain at least one sulphonyl substituent but preferably the product does not contain more than one sulphonic acid group. O, o1- dihydroxy-#s-carboxy -#s1- hydroxy and #shydroxy- #s1-amino-azo are the dyestuffs used although dye-stuffs containing a group convertible into a hydroxyl group during metallisation, such as #s-hydroxy- #s1- halogen or -alkoxydyestuffs, may also be used. Chromium, cobalt and nickel are specified metals the former being preferred. Metallisation is effected by conventional processes. Indicated as mono-azo dyestuffs are the coupling products of diazotized #s-amino-phenols and -naphthols with acyl acetic acid arylamides, 5- pyrazolones, 2, 4- dihydroxyquinolines, benzene and naphthalene compounds coupling #s to a hydroxyl group and coupling products of diazotized #saminoaryl carboxylic acids with 5-pyrazolones or benzene and naphthalene compounds which couple #s to a hydroxy group. Indicated as disazo dyestuffs are compounds formed from diazotized 4- or 5- arylazo -2-aminophenols and 5- pyrazolones or naphthols or phenols which couple #s to a hydroxy group, disazo dyestuffs having a metallizable group with m-dihydroxy or -diaminobenzenes or aminonaphthols as coupling components and those obtained from diazotized 4- arylazo -2- alkyloxy-1- naphthylamines and azo components coupling in an adjacent position to a hydroxy group. Indicated as substituents for the dyestuff molecules are halogen, alkyl, alkoxy, nitro, acylamino, carboxy, sulphonic acid, sulphonamide, acyl and alkyl- and arylsulphonyl. The metalfree dyestuff is added to the metal-containing dyestuff with components which are only partly soluble in water. The addition is advantageously effected in aqueous solution at 40-95 DEG C. in the presence of alkaline agents or agents which buffer mineral acid. The products are deep brown to black in colour. The dyestuffs are used to colour wool, silk, leather, furs, casein, polypeptides, superpolyamides and -urethanes, paper, lacquers and cellulosic spinning masses. Examples and a Table are provided illustrating the preparation of the dyestuffs and their use in dyeing processes, representative of the monoazo dyestuffs used are 2-aminophenol -4- methyl sulphone --> 1- phenyl -3- methyl -5- pyrazolone, 4-nitro -2- aminophenol --> 3, 4- dimethyl phenol, 1- amino- 4- sulpho -6- nitro -2- naphthol --> 2-naphthol, 4- nitro -2- aminophenol --> 2- naphthol, 5- nitro -2- aminophenol --> 2- naphthylamine and 2- amino -1- carboxybenzene -4-sulphonic acid --> 2- naphthol, and representative of the disazo dyestuffs are 3- amino -4- hydroxyazobenzene -41- sulphonic acid dimethylamide --> 2- naphthol, 2- methoxy -4- nitro-aniline <FORM:0851861/IV (c)/1> 2- amino -5- naphthol <FORM:0851861/IV (c)/2> anthranilic acid, 4-amino -3- carboxy -41- chlorazobenzene --> 2-naphthol and 5- nitro -2- aminophenol --> 1-phenylazo -2- amino -snaphthol 7- sulphonic acid. Specification 791,438 is disclaimed. Reference has been directed by the Comptroller to Specification 667,168.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH851861X | 1956-01-26 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB851861A true GB851861A (en) | 1960-10-19 |
Family
ID=4542357
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB2739/57A Expired GB851861A (en) | 1956-01-26 | 1957-01-25 | Improvements relating to heavy metal-containing azo dyestuffs and their use |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB851861A (en) |
Cited By (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3398132A (en) * | 1964-10-29 | 1968-08-20 | Basf Ag | 1:2-chromium complex mixed azo dyes |
US3525732A (en) * | 1966-05-06 | 1970-08-25 | Geigy Ag J R | 1:2 chromium complex dyestuffs containing a monoazo dyestuff and disazo dyestuff |
US4150942A (en) * | 1976-05-31 | 1979-04-24 | Sandoz Ltd. | 1:2 Metal complexes of azo compounds having 1-hydroxynaphthalene-3-sulfonic acid coupling component radicals at least one of which is a disazo compound |
US4537955A (en) * | 1982-03-02 | 1985-08-27 | Basf Aktiengesellschaft | Unsymmetrical 1:2 chromium complex of a monoazo dyestuff and a disazo dyestuff which is non-fiber reactive and contains no sulfonamido or amino groups |
EP0718374A1 (en) | 1994-12-21 | 1996-06-26 | Ciba-Geigy Ag | 1:2-Chromecomplex dyestuffs containing dyestuff-mixtures and 1:2-chromecomplex dyestuffs |
US6428582B1 (en) | 1993-05-18 | 2002-08-06 | Ciba Specialty Chemicals Corporation | Dye mixtures, 1:2 cobalt complex formazan dyes and their use |
US6551364B2 (en) | 1993-05-18 | 2003-04-22 | Ciba Specialty Chemicals Corporation | Dye mixtures, 1:2 cobalt complex formazan dyes and their use |
WO2006042802A1 (en) | 2004-10-19 | 2006-04-27 | Huntsman Advanced Materials (Switzerland) Gmbh | Reactive dyes, their preparation and their use |
WO2010084044A1 (en) | 2009-01-21 | 2010-07-29 | Huntsman Advanced Materials (Switzerland) Gmbh | Reactive dyes, their preparation and their use |
WO2013182349A1 (en) | 2012-06-05 | 2013-12-12 | Huntsman Advanced Materials (Switzerland) Gmbh | Reactive dyes, their preparation and their use |
-
1957
- 1957-01-25 GB GB2739/57A patent/GB851861A/en not_active Expired
Cited By (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3398132A (en) * | 1964-10-29 | 1968-08-20 | Basf Ag | 1:2-chromium complex mixed azo dyes |
US3525732A (en) * | 1966-05-06 | 1970-08-25 | Geigy Ag J R | 1:2 chromium complex dyestuffs containing a monoazo dyestuff and disazo dyestuff |
US4150942A (en) * | 1976-05-31 | 1979-04-24 | Sandoz Ltd. | 1:2 Metal complexes of azo compounds having 1-hydroxynaphthalene-3-sulfonic acid coupling component radicals at least one of which is a disazo compound |
US4537955A (en) * | 1982-03-02 | 1985-08-27 | Basf Aktiengesellschaft | Unsymmetrical 1:2 chromium complex of a monoazo dyestuff and a disazo dyestuff which is non-fiber reactive and contains no sulfonamido or amino groups |
US6428582B1 (en) | 1993-05-18 | 2002-08-06 | Ciba Specialty Chemicals Corporation | Dye mixtures, 1:2 cobalt complex formazan dyes and their use |
US6551364B2 (en) | 1993-05-18 | 2003-04-22 | Ciba Specialty Chemicals Corporation | Dye mixtures, 1:2 cobalt complex formazan dyes and their use |
EP0718374A1 (en) | 1994-12-21 | 1996-06-26 | Ciba-Geigy Ag | 1:2-Chromecomplex dyestuffs containing dyestuff-mixtures and 1:2-chromecomplex dyestuffs |
US5667534A (en) * | 1994-12-21 | 1997-09-16 | Ciba-Geigy Corporation | Dye mixtures comprising 1:2 chromium complex dyes, and 1:2 chromium complex dyes |
WO2006042802A1 (en) | 2004-10-19 | 2006-04-27 | Huntsman Advanced Materials (Switzerland) Gmbh | Reactive dyes, their preparation and their use |
WO2010084044A1 (en) | 2009-01-21 | 2010-07-29 | Huntsman Advanced Materials (Switzerland) Gmbh | Reactive dyes, their preparation and their use |
US8348412B2 (en) | 2009-01-21 | 2013-01-08 | Huntsman International Llc | Reactive dyes, their preparation and their use |
WO2013182349A1 (en) | 2012-06-05 | 2013-12-12 | Huntsman Advanced Materials (Switzerland) Gmbh | Reactive dyes, their preparation and their use |
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