DE165139C - - Google Patents
Info
- Publication number
- DE165139C DE165139C DE1901165139D DE165139DA DE165139C DE 165139 C DE165139 C DE 165139C DE 1901165139 D DE1901165139 D DE 1901165139D DE 165139D A DE165139D A DE 165139DA DE 165139 C DE165139 C DE 165139C
- Authority
- DE
- Germany
- Prior art keywords
- blue
- green
- dye
- color
- heated
- 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 - Lifetime
Links
- 238000000034 method Methods 0.000 claims description 7
- 150000002828 nitro derivatives Chemical class 0.000 claims description 2
- 150000003142 primary aromatic amines Chemical class 0.000 claims description 2
- RZXMPPFPUUCRFN-UHFFFAOYSA-N p-toluidine Chemical compound CC1=CC=C(N)C=C1 RZXMPPFPUUCRFN-UHFFFAOYSA-N 0.000 description 11
- 239000000975 dye Substances 0.000 description 9
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 8
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 7
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 7
- 239000000155 melt Substances 0.000 description 6
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 5
- AFBPFSWMIHJQDM-UHFFFAOYSA-N N-methyl-N-phenylamine Natural products CNC1=CC=CC=C1 AFBPFSWMIHJQDM-UHFFFAOYSA-N 0.000 description 5
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- 235000019441 ethanol Nutrition 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 3
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 3
- ZYECOAILUNWEAL-NUDFZHEQSA-N (4z)-4-[[2-methoxy-5-(phenylcarbamoyl)phenyl]hydrazinylidene]-n-(3-nitrophenyl)-3-oxonaphthalene-2-carboxamide Chemical compound COC1=CC=C(C(=O)NC=2C=CC=CC=2)C=C1N\N=C(C1=CC=CC=C1C=1)/C(=O)C=1C(=O)NC1=CC=CC([N+]([O-])=O)=C1 ZYECOAILUNWEAL-NUDFZHEQSA-N 0.000 description 2
- ZXVONLUNISGICL-UHFFFAOYSA-N 4,6-dinitro-o-cresol Chemical group CC1=CC([N+]([O-])=O)=CC([N+]([O-])=O)=C1O ZXVONLUNISGICL-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 239000001045 blue dye Substances 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 238000009833 condensation Methods 0.000 description 2
- 230000005494 condensation Effects 0.000 description 2
- 239000013078 crystal Substances 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 230000000802 nitrating effect Effects 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 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 2
- 150000003973 alkyl amines Chemical class 0.000 description 1
- 125000003282 alkyl amino group Chemical group 0.000 description 1
- 125000003368 amide group Chemical group 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 150000004982 aromatic amines Chemical class 0.000 description 1
- 125000005264 aryl amine group Chemical group 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 238000005121 nitriding Methods 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-N sulfonic acid Chemical compound OS(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-N 0.000 description 1
- 210000002268 wool Anatomy 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
- C09B1/16—Amino-anthraquinones
- C09B1/20—Preparation from starting materials already containing the anthracene nucleus
- C09B1/26—Dyes with amino groups substituted by hydrocarbon radicals
- C09B1/32—Dyes with amino groups substituted by hydrocarbon radicals substituted by aryl groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| AT27445D AT27445B (de) | 1901-04-06 | 1905-10-13 | Verfahren zur Darstellung von Farbstoffen der Anthrazenreihe. |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE165139C true DE165139C (cs) |
Family
ID=430669
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE1901165139D Expired - Lifetime DE165139C (cs) | 1901-04-06 | 1901-04-06 |
Country Status (1)
| Country | Link |
|---|---|
| DE (1) | DE165139C (cs) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2587002A (en) * | 1947-04-22 | 1952-02-26 | Celanese Corp | Anthraquinone dyestuffs |
-
1901
- 1901-04-06 DE DE1901165139D patent/DE165139C/de not_active Expired - Lifetime
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2587002A (en) * | 1947-04-22 | 1952-02-26 | Celanese Corp | Anthraquinone dyestuffs |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE963265C (de) | Verfahren zur Herstellung von Anthrachinonfarbstoffen | |
| DE165139C (cs) | ||
| DE403395C (de) | Verfahren zur Herstellung von Kuepenfarbstoffen der Anthrachinonreihe | |
| AT27445B (de) | Verfahren zur Darstellung von Farbstoffen der Anthrazenreihe. | |
| DE144634C (cs) | ||
| DE86150C (de) | Verfahren zur einführung von aminresten in oxyanthrachinone | |
| DE126542C (cs) | ||
| DE136778C (cs) | ||
| DE167410C (cs) | ||
| DE109261C (cs) | ||
| DE288464C (cs) | ||
| DE131873C (cs) | ||
| DE139581C (cs) | ||
| DE516784C (de) | Verfahren zur Darstellung von Kuepenfarbstoffen der 1íñ2-Benzanthrachinonreihe | |
| DE558474C (de) | Verfahren zur Darstellung von Derivaten des 1, 1-Dianthrachinonyls | |
| DE69785C (de) | Verfahren zur Darstellung von Farbstoffen der Indulinreihe aus symmetrischen p-Diatnidodialkylthioharnstoffen | |
| DE164791C (cs) | ||
| DE510435C (de) | Verfahren zur Darstellung von negativ substituierten Carbazolen | |
| DE40420C (de) | Verfahren zur Darstellung rolher Farbstoffe aus IsochinoVin | |
| DE83085C (cs) | ||
| DE125578C (cs) | ||
| DE162824C (de) | Verfahren zur Darstellung von Dianthrachinonimiden | |
| DE181723C (cs) | ||
| DE118609C (cs) | ||
| DE78497C (de) | Verfahren zur Darstellung von basischen Farbstoffen und deren Sulfosäuren aus phettylirten o.\ /Si-Naphtylendiaminen |