DK141408B - Farvesalte, opløselige i organiske opløsningsmidler, til anvendelse i farvende opløsninger. - Google Patents
Farvesalte, opløselige i organiske opløsningsmidler, til anvendelse i farvende opløsninger. Download PDFInfo
- Publication number
- DK141408B DK141408B DK393172AA DK393172A DK141408B DK 141408 B DK141408 B DK 141408B DK 393172A A DK393172A A DK 393172AA DK 393172 A DK393172 A DK 393172A DK 141408 B DK141408 B DK 141408B
- Authority
- DK
- Denmark
- Prior art keywords
- primene
- dye
- amino
- color
- sulfonic acid
- Prior art date
Links
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- 125000002339 acetoacetyl group Chemical group O=C([*])C([H])([H])C(=O)C([H])([H])[H] 0.000 description 1
- 229940081735 acetylcellulose Drugs 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 150000001299 aldehydes Chemical class 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 125000004453 alkoxycarbonyl group Chemical group 0.000 description 1
- 125000003282 alkyl amino group Chemical group 0.000 description 1
- 125000005037 alkyl phenyl group Chemical group 0.000 description 1
- 125000004390 alkyl sulfonyl group Chemical group 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 229940051880 analgesics and antipyretics pyrazolones Drugs 0.000 description 1
- 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 1
- 239000001000 anthraquinone dye Substances 0.000 description 1
- 150000004056 anthraquinones Chemical class 0.000 description 1
- 239000012431 aqueous reaction media Substances 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 208000010668 atopic eczema Diseases 0.000 description 1
- 239000001009 azin dye Substances 0.000 description 1
- 125000000751 azo group Chemical group [*]N=N[*] 0.000 description 1
- 150000001555 benzenes Chemical class 0.000 description 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- 125000005587 carbonate group Chemical group 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 150000001733 carboxylic acid esters Chemical class 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920002301 cellulose acetate Polymers 0.000 description 1
- 229920003086 cellulose ether Polymers 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 150000001844 chromium Chemical class 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 235000019864 coconut oil Nutrition 0.000 description 1
- 239000003240 coconut oil Substances 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 230000001335 demethylating effect Effects 0.000 description 1
- 125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 description 1
- GGSUCNLOZRCGPQ-UHFFFAOYSA-N diethylaniline Chemical compound CCN(CC)C1=CC=CC=C1 GGSUCNLOZRCGPQ-UHFFFAOYSA-N 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 1
- QKIUAMUSENSFQQ-UHFFFAOYSA-N dimethylazanide Chemical compound C[N-]C QKIUAMUSENSFQQ-UHFFFAOYSA-N 0.000 description 1
- PPSZHCXTGRHULJ-UHFFFAOYSA-N dioxazine Chemical compound O1ON=CC=C1 PPSZHCXTGRHULJ-UHFFFAOYSA-N 0.000 description 1
- 150000005125 dioxazines Chemical class 0.000 description 1
- KZTYYGOKRVBIMI-UHFFFAOYSA-N diphenyl sulfone Chemical group C=1C=CC=CC=1S(=O)(=O)C1=CC=CC=C1 KZTYYGOKRVBIMI-UHFFFAOYSA-N 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 150000002148 esters Chemical group 0.000 description 1
- 229920001249 ethyl cellulose Polymers 0.000 description 1
- 235000019325 ethyl cellulose Nutrition 0.000 description 1
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 1
- IVJISJACKSSFGE-UHFFFAOYSA-N formaldehyde;1,3,5-triazine-2,4,6-triamine Chemical compound O=C.NC1=NC(N)=NC(N)=N1 IVJISJACKSSFGE-UHFFFAOYSA-N 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 150000008282 halocarbons Chemical class 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 125000005059 halophenyl group Chemical group 0.000 description 1
- RBTKNAXYKSUFRK-UHFFFAOYSA-N heliogen blue Chemical compound [Cu].[N-]1C2=C(C=CC=C3)C3=C1N=C([N-]1)C3=CC=CC=C3C1=NC([N-]1)=C(C=CC=C3)C3=C1N=C([N-]1)C3=CC=CC=C3C1=N2 RBTKNAXYKSUFRK-UHFFFAOYSA-N 0.000 description 1
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 238000007641 inkjet printing Methods 0.000 description 1
- 238000010409 ironing Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000001465 metallisation Methods 0.000 description 1
- 125000001434 methanylylidene group Chemical group [H]C#[*] 0.000 description 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
- ABBNXJIPPYAOSC-UHFFFAOYSA-N n-(2-hydroxynaphthalen-1-yl)acetamide Chemical compound C1=CC=C2C(NC(=O)C)=C(O)C=CC2=C1 ABBNXJIPPYAOSC-UHFFFAOYSA-N 0.000 description 1
- 239000000025 natural resin Substances 0.000 description 1
- 239000001005 nitro dye Substances 0.000 description 1
- 229920001220 nitrocellulos Polymers 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- NRZWYNLTFLDQQX-UHFFFAOYSA-N p-tert-Amylphenol Chemical compound CCC(C)(C)C1=CC=C(O)C=C1 NRZWYNLTFLDQQX-UHFFFAOYSA-N 0.000 description 1
- NTPSQPZXFVRULZ-UHFFFAOYSA-N pentadecan-8-amine Chemical compound CCCCCCCC(N)CCCCCCC NTPSQPZXFVRULZ-UHFFFAOYSA-N 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- WVDDGKGOMKODPV-ZQBYOMGUSA-N phenyl(114C)methanol Chemical compound O[14CH2]C1=CC=CC=C1 WVDDGKGOMKODPV-ZQBYOMGUSA-N 0.000 description 1
- 239000004584 polyacrylic acid Substances 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920000768 polyamine Polymers 0.000 description 1
- 238000006068 polycondensation reaction Methods 0.000 description 1
- ODGAOXROABLFNM-UHFFFAOYSA-N polynoxylin Chemical compound O=C.NC(N)=O ODGAOXROABLFNM-UHFFFAOYSA-N 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 235000013772 propylene glycol Nutrition 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 150000003335 secondary amines Chemical class 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- ORFSSYGWXNGVFB-UHFFFAOYSA-N sodium 4-amino-6-[[4-[4-[(8-amino-1-hydroxy-5,7-disulfonaphthalen-2-yl)diazenyl]-3-methoxyphenyl]-2-methoxyphenyl]diazenyl]-5-hydroxynaphthalene-1,3-disulfonic acid Chemical compound COC1=C(C=CC(=C1)C2=CC(=C(C=C2)N=NC3=C(C4=C(C=C3)C(=CC(=C4N)S(=O)(=O)O)S(=O)(=O)O)O)OC)N=NC5=C(C6=C(C=C5)C(=CC(=C6N)S(=O)(=O)O)S(=O)(=O)O)O.[Na+] ORFSSYGWXNGVFB-UHFFFAOYSA-N 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000010186 staining Methods 0.000 description 1
- 239000012192 staining solution Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 description 1
- 238000006277 sulfonation reaction Methods 0.000 description 1
- 150000003457 sulfones Chemical class 0.000 description 1
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- YBRBMKDOPFTVDT-UHFFFAOYSA-N tert-butylamine Chemical compound CC(C)(C)N YBRBMKDOPFTVDT-UHFFFAOYSA-N 0.000 description 1
- 239000010981 turquoise Substances 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 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
- C09B69/00—Dyes not provided for by a single group of this subclass
- C09B69/02—Dyestuff salts, e.g. salts of acid dyes with basic dyes
- C09B69/04—Dyestuff salts, e.g. salts of acid dyes with basic dyes of anionic dyes with nitrogen containing compounds
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH1173071 | 1971-08-10 | ||
| CH1173071A CH566382A5 (en) | 1971-08-10 | 1971-08-10 | Dyestuffs - comprising amine salts of anionic dyes, with good alcohol solubility |
| CH1480471 | 1971-10-11 | ||
| CH1480471 | 1971-10-11 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| DK141408B true DK141408B (da) | 1980-03-10 |
| DK141408C DK141408C (oth) | 1980-09-08 |
Family
ID=25708825
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DK393172AA DK141408B (da) | 1971-08-10 | 1972-08-09 | Farvesalte, opløselige i organiske opløsningsmidler, til anvendelse i farvende opløsninger. |
Country Status (12)
| Country | Link |
|---|---|
| US (1) | US4322529A (oth) |
| JP (1) | JPS5748590B2 (oth) |
| AR (1) | AR194744A1 (oth) |
| BE (1) | BE787351A (oth) |
| CA (1) | CA994331A (oth) |
| DE (1) | DE2238773C3 (oth) |
| DK (1) | DK141408B (oth) |
| ES (1) | ES405674A1 (oth) |
| FR (1) | FR2148560B1 (oth) |
| GB (1) | GB1392572A (oth) |
| IT (1) | IT963860B (oth) |
| NL (1) | NL173862C (oth) |
Families Citing this family (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NL7408543A (nl) * | 1973-07-05 | 1975-01-07 | Basf Ag | Werkwijze ter bereiding van isotridecylammo- niumzouten van complexe chroom- of kobalt-1:2- -azokleurstoffen. |
| DE2341293C3 (de) * | 1973-08-16 | 1981-10-08 | Bayer Ag, 5090 Leverkusen | Anionische Farbstoffe und konzentrierte Lösungen dieser Farbstoffe |
| GB1549751A (en) * | 1976-12-09 | 1979-08-08 | Williams Ltd | Amino acid salts of anionic dyes and processes for their preparation |
| DE3416327A1 (de) * | 1984-05-03 | 1985-11-07 | Basf Ag, 6700 Ludwigshafen | Farbsalze sulfonsaeuregruppenhaltiger polyazofarbstoffe |
| DE3578431D1 (de) * | 1984-05-03 | 1990-08-02 | Basf Ag | Farbsalze anionischer farbstoffe. |
| US5510467A (en) * | 1989-01-03 | 1996-04-23 | Sandoz Ltd. | Salts of metal-free anionic phenylazopyrazolone dyes having cations containing sterically hindered amine groups |
| GB2259305B (en) * | 1991-09-05 | 1995-11-15 | Sandoz Ltd | 2:1 aluminium complexes |
| CN1720298A (zh) * | 2002-12-05 | 2006-01-11 | 西巴特殊化学品控股有限公司 | 基于苯并咪唑－吡啶酮的偶氮染料 |
| JP5080984B2 (ja) * | 2004-12-29 | 2012-11-21 | チバ ホールディング インコーポレーテッド | 有機溶媒に可溶性である染料 |
| US7294730B2 (en) * | 2005-11-30 | 2007-11-13 | Xerox Corporation | Colorant compounds |
| US7381255B2 (en) * | 2005-11-30 | 2008-06-03 | Xerox Corporation | Phase change inks |
| US7442242B2 (en) * | 2005-11-30 | 2008-10-28 | Xerox Corporation | Phase change inks containing specific colorants |
| DE102010012047A1 (de) * | 2010-03-19 | 2011-09-22 | Basf Coatings Gmbh | Verfahren zur Beschichtung eines Metall- oder Kunststoffsubstrats, daraus erhältliche Beschichtung und beschichtetes Substrat |
Family Cites Families (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US1811160A (en) * | 1928-06-05 | 1931-06-23 | Continental Can Co | Container for food products |
| FR873214A (fr) * | 1938-11-05 | 1942-07-02 | Ig Farbenindustrie Ag | Matières colorantes solubles dans les solvants organiques |
| US2315870A (en) * | 1938-11-05 | 1943-04-06 | Gen Aniline & Film Corp | Isoalkylamine salts of organic sulphonic or carboxylic acids |
| DE767788C (de) * | 1938-11-06 | 1953-06-22 | Ig Farbenindustrie Ag | Verfahren zur Herstellung von Farbstoffsalzen |
| US2490703A (en) * | 1946-05-01 | 1949-12-06 | Gen Aniline & Film Corp | Salts of organic dyestuffs |
| US3066063A (en) * | 1957-10-17 | 1962-11-27 | American Can Co | Method of forming longitudinally extending side seams in a tubular container |
| US2990405A (en) * | 1959-05-26 | 1961-06-27 | American Cyanamid Co | Spirit soluble black dyes |
| FR1297014A (fr) * | 1960-08-09 | 1962-06-22 | Basf Ag | Sels d'ammonium de colorants à complexes métalliques |
| NL129233C (oth) * | 1965-01-15 | |||
| NL130115C (oth) * | 1965-12-10 | 1970-06-15 | ||
| DE2051303C3 (de) * | 1970-10-20 | 1978-12-21 | Bayer Ag, 5090 Leverkusen | Polyhydroxyalkylaminsalze anionischer Farbstoffe |
| US3994872A (en) * | 1971-08-10 | 1976-11-30 | Ciba-Geigy Corporation | Tertiary-alkylamine salts of metal complex dyestuffs |
-
1972
- 1972-07-26 NL NLAANVRAGE7210304,A patent/NL173862C/xx not_active IP Right Cessation
- 1972-08-01 CA CA148,387A patent/CA994331A/en not_active Expired
- 1972-08-07 DE DE2238773A patent/DE2238773C3/de not_active Expired
- 1972-08-08 GB GB3695372A patent/GB1392572A/en not_active Expired
- 1972-08-08 AR AR243477A patent/AR194744A1/es active
- 1972-08-09 DK DK393172AA patent/DK141408B/da not_active IP Right Cessation
- 1972-08-09 IT IT28035/72A patent/IT963860B/it active
- 1972-08-09 ES ES405674A patent/ES405674A1/es not_active Expired
- 1972-08-09 JP JP47079867A patent/JPS5748590B2/ja not_active Expired
- 1972-08-09 BE BE787351D patent/BE787351A/xx not_active IP Right Cessation
- 1972-08-09 FR FR7228705A patent/FR2148560B1/fr not_active Expired
-
1977
- 1977-11-16 US US05/851,924 patent/US4322529A/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| GB1392572A (en) | 1975-04-30 |
| DE2238773A1 (de) | 1973-02-22 |
| DK141408C (oth) | 1980-09-08 |
| DE2238773B2 (de) | 1979-03-01 |
| US4322529A (en) | 1982-03-30 |
| JPS5748590B2 (oth) | 1982-10-16 |
| FR2148560B1 (oth) | 1975-03-07 |
| JPS4826218A (oth) | 1973-04-06 |
| CA994331A (en) | 1976-08-03 |
| DE2238773C3 (de) | 1979-10-25 |
| NL173862B (nl) | 1983-10-17 |
| FR2148560A1 (oth) | 1973-03-23 |
| ES405674A1 (es) | 1976-01-16 |
| BE787351A (fr) | 1973-02-09 |
| NL7210304A (oth) | 1973-02-13 |
| AR194744A1 (es) | 1973-08-14 |
| NL173862C (nl) | 1984-03-16 |
| IT963860B (it) | 1974-01-21 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PBP | Patent lapsed |