DE251115C - - Google Patents
Info
- Publication number
- DE251115C DE251115C DENDAT251115D DE251115DA DE251115C DE 251115 C DE251115 C DE 251115C DE NDAT251115 D DENDAT251115 D DE NDAT251115D DE 251115D A DE251115D A DE 251115DA DE 251115 C DE251115 C DE 251115C
- Authority
- DE
- Germany
- Prior art keywords
- parts
- blue
- alcohol
- red
- sulfuric acid
- 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.)
- Active
Links
- -1 aryl mercaptans Chemical class 0.000 claims description 5
- 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 claims description 4
- 150000004056 anthraquinones Chemical class 0.000 claims description 4
- 238000000034 method Methods 0.000 claims description 3
- 125000001424 substituent group Chemical group 0.000 claims description 3
- 150000001454 anthracenes Chemical class 0.000 claims description 2
- 238000002360 preparation method Methods 0.000 claims description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims 1
- 239000007859 condensation product Substances 0.000 claims 1
- 229910052717 sulfur Inorganic materials 0.000 claims 1
- 239000011593 sulfur Substances 0.000 claims 1
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 18
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 7
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 7
- WLHCBQAPPJAULW-UHFFFAOYSA-N 4-methylbenzenethiol Chemical compound CC1=CC=C(S)C=C1 WLHCBQAPPJAULW-UHFFFAOYSA-N 0.000 description 6
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 6
- 239000003960 organic solvent Substances 0.000 description 6
- 235000011118 potassium hydroxide Nutrition 0.000 description 6
- 239000000975 dye Substances 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- 239000000203 mixture Substances 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 3
- 239000013078 crystal Substances 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- 239000007795 chemical reaction product Substances 0.000 description 2
- 239000000049 pigment Substances 0.000 description 2
- 239000007858 starting material Substances 0.000 description 2
- IIPRUQZTMZETSL-UHFFFAOYSA-N 1-bromo-4-(methylamino)anthracene-9,10-dione Chemical compound O=C1C2=CC=CC=C2C(=O)C2=C1C(Br)=CC=C2NC IIPRUQZTMZETSL-UHFFFAOYSA-N 0.000 description 1
- YWYHGNUFMPSTTR-UHFFFAOYSA-N 1-methyl-4-(4-methylphenoxy)benzene Chemical compound C1=CC(C)=CC=C1OC1=CC=C(C)C=C1 YWYHGNUFMPSTTR-UHFFFAOYSA-N 0.000 description 1
- PLGPRGMWHYWEFT-UHFFFAOYSA-N 2-amino-1-chloroanthracene-9,10-dione Chemical compound C1=CC=C2C(=O)C3=C(Cl)C(N)=CC=C3C(=O)C2=C1 PLGPRGMWHYWEFT-UHFFFAOYSA-N 0.000 description 1
- 244000003034 Arancio amaro Species 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 235000019646 color tone Nutrition 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 125000005000 thioaryl group Chemical group 0.000 description 1
- SWGJCIMEBVHMTA-UHFFFAOYSA-K trisodium;6-oxido-4-sulfo-5-[(4-sulfonatonaphthalen-1-yl)diazenyl]naphthalene-2-sulfonate Chemical compound [Na+].[Na+].[Na+].C1=CC=C2C(N=NC3=C4C(=CC(=CC4=CC=C3O)S([O-])(=O)=O)S([O-])(=O)=O)=CC=C(S([O-])(=O)=O)C2=C1 SWGJCIMEBVHMTA-UHFFFAOYSA-K 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
- C09B1/00—Dyes with anthracene nucleus not condensed with any other ring
- C09B1/56—Mercapto-anthraquinones
- C09B1/58—Mercapto-anthraquinones with mercapto groups substituted by aliphatic, cycloaliphatic, araliphatic or aryl radicals
- C09B1/585—Mercapto-anthraquinones with mercapto groups substituted by aliphatic, cycloaliphatic, araliphatic or aryl radicals substituted by aryl radicals
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Coloring (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE440698T | 1911-05-30 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE251115C true DE251115C (en:Method) |
Family
ID=8900061
Family Applications (3)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DENDAT251115D Active DE251115C (en:Method) | 1911-05-30 | ||
| DENDAT251709D Active DE251709C (en:Method) | 1911-05-30 | ||
| DENDAT250273D Active DE250273C (en:Method) | 1911-05-30 |
Family Applications After (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DENDAT251709D Active DE251709C (en:Method) | 1911-05-30 | ||
| DENDAT250273D Active DE250273C (en:Method) | 1911-05-30 |
Country Status (2)
| Country | Link |
|---|---|
| DE (3) | DE250273C (en:Method) |
| FR (1) | FR440698A (en:Method) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2640060A (en) * | 1949-09-09 | 1953-05-26 | Celanese Corp | Beta-hydroxyethyl-thioanthraquinones |
| US3018154A (en) * | 1959-09-24 | 1962-01-23 | Allied Chem | Colored aromatic polyester material and process of making same |
| US5579698A (en) * | 1995-11-27 | 1996-12-03 | Lis; Henry | Transportation and installation device for heavy pipes |
-
0
- DE DENDAT251115D patent/DE251115C/de active Active
- DE DENDAT251709D patent/DE251709C/de active Active
- DE DENDAT250273D patent/DE250273C/de active Active
-
1912
- 1912-02-27 FR FR440698A patent/FR440698A/fr not_active Expired
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2640060A (en) * | 1949-09-09 | 1953-05-26 | Celanese Corp | Beta-hydroxyethyl-thioanthraquinones |
| US3018154A (en) * | 1959-09-24 | 1962-01-23 | Allied Chem | Colored aromatic polyester material and process of making same |
| US5579698A (en) * | 1995-11-27 | 1996-12-03 | Lis; Henry | Transportation and installation device for heavy pipes |
Also Published As
| Publication number | Publication date |
|---|---|
| DE250273C (en:Method) | |
| FR440698A (fr) | 1912-07-17 |
| DE251709C (en:Method) |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE251115C (en:Method) | ||
| DE550645C (de) | Verfahren zur Darstellung von Farbstoffen | |
| DE536294C (de) | Verfahren zur Darstellung von Kuepenfarbstoffen der Anthrachinonreihe | |
| DE517278C (de) | Verfahren zur Darstellung von neuen Kuepenfarbstoffen | |
| DE504017C (de) | Verfahren zur Herstellung von gefaerbten Komplexverbindungen, insbesondere von Pigmentfarbstoffen | |
| DE1669083B2 (de) | Farbstoffzubereitungen für Schreib- und Druckzwecke | |
| DE613896C (de) | Verfahren zur Herstellung von Selenverbindungen der Benzanthronreihe | |
| DE227105C (en:Method) | ||
| DE670259C (de) | Verfahren zur Herstellung von Monoazofarbstoffen | |
| DE495115C (de) | Verfahren zur Darstellung von rotorange bis braunrot faerbenden basischen Farbstoffen | |
| DE662462C (de) | Verfahren zur Herstellung von Kuepenfarbstoffen der Dipyrazolanthronreihe | |
| DE149322C (en:Method) | ||
| DE646299C (de) | Verfahren zur Herstellung von Alkylaminen der Anthrachinonreihe | |
| DE634041C (de) | Verfahren zur Herstellung von Farbstoffen der Thioindigoreihe | |
| DE212594C (en:Method) | ||
| DE278423C (en:Method) | ||
| DE253091C (en:Method) | ||
| DE79320C (de) | Verfahren zur Darstellung grünblauer i Beizenfarbstoffe ausTetralkyldiamidobenzhydrolen | |
| DE535092C (de) | Verfahren zur Darstellung von halogenhaltigen Kuepenfarbstoffen | |
| DE470949C (de) | Verfahren zur Darstellung stickstoffhaltiger Kuepenfarbstoffe | |
| DE516784C (de) | Verfahren zur Darstellung von Kuepenfarbstoffen der 1íñ2-Benzanthrachinonreihe | |
| DE719639C (de) | Verfahren zur Herstellung von Manganoxyde und Bariumoxyd enthaltenden Pigmenten | |
| US1531263A (en) | Production of coloring matters | |
| DE245973C (en:Method) | ||
| DE590873C (de) | Verfahren zur Darstellung von Schwefelfarbstoffen |