DE267418C - - Google Patents
Info
- Publication number
- DE267418C DE267418C DENDAT267418D DE267418DA DE267418C DE 267418 C DE267418 C DE 267418C DE NDAT267418 D DENDAT267418 D DE NDAT267418D DE 267418D A DE267418D A DE 267418DA DE 267418 C DE267418 C DE 267418C
- Authority
- DE
- Germany
- Prior art keywords
- violet
- blue
- aminoviolanthrene
- parts
- amino
- 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
- 150000001412 amines Chemical class 0.000 claims description 4
- 239000000984 vat dye Substances 0.000 claims description 3
- 125000003277 amino group Chemical group 0.000 claims description 2
- HUKPVYBUJRAUAG-UHFFFAOYSA-N 7-benzo[a]phenalenone Chemical class C1=CC(C(=O)C=2C3=CC=CC=2)=C2C3=CC=CC2=C1 HUKPVYBUJRAUAG-UHFFFAOYSA-N 0.000 claims 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 1
- 229910052739 hydrogen Inorganic materials 0.000 claims 1
- 239000001257 hydrogen Substances 0.000 claims 1
- 239000000975 dye Substances 0.000 description 5
- YDQNUMLZOCJDKZ-UHFFFAOYSA-N violanthren-1-ylamine Chemical compound C1C(C2=C34)=CC=C3C(C3=C56)=CC=C5CC5=CC=CC=C5C6=CC=C3C4=CC=C2C2=C1C=CC=C2N YDQNUMLZOCJDKZ-UHFFFAOYSA-N 0.000 description 5
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 4
- GZUWHLLVZWEXDX-UHFFFAOYSA-N isoviolanthren-1-ylamine Chemical compound C1C(C2=C34)=CC=C3C(C3=C56)=CC=C5C5=CC=CC=C5CC6=CC=C3C4=CC=C2C2=C1C(N)=CC=C2 GZUWHLLVZWEXDX-UHFFFAOYSA-N 0.000 description 4
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 3
- 241000394591 Hybanthus Species 0.000 description 3
- -1 iodoethyl Chemical group 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- 240000009038 Viola odorata Species 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- PASDCCFISLVPSO-UHFFFAOYSA-N benzoyl chloride Chemical compound ClC(=O)C1=CC=CC=C1 PASDCCFISLVPSO-UHFFFAOYSA-N 0.000 description 2
- KCXMKQUNVWSEMD-UHFFFAOYSA-N benzyl chloride Chemical compound ClCC1=CC=CC=C1 KCXMKQUNVWSEMD-UHFFFAOYSA-N 0.000 description 2
- 229940073608 benzyl chloride Drugs 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 241000131971 Bradyrhizobiaceae Species 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 235000005811 Viola adunca Nutrition 0.000 description 1
- 235000013487 Viola odorata Nutrition 0.000 description 1
- 235000002254 Viola papilionacea Nutrition 0.000 description 1
- 244000172533 Viola sororia Species 0.000 description 1
- 125000002877 alkyl aryl group Chemical group 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- GRWZHXKQBITJKP-UHFFFAOYSA-L dithionite(2-) Chemical compound [O-]S(=O)S([O-])=O GRWZHXKQBITJKP-UHFFFAOYSA-L 0.000 description 1
- 239000008098 formaldehyde solution Substances 0.000 description 1
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 description 1
- HKSRHNHDUAHAAT-UHFFFAOYSA-N isoviolanthrene Chemical compound C12=C3C4=CC=C2CC2=CC=CC=C2C1=CC=C3C1=CC=C2CC3=CC=CC=C3C3=CC=C4C1=C32 HKSRHNHDUAHAAT-UHFFFAOYSA-N 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 239000007800 oxidant agent Substances 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 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
- JAIHDOVRCZNXDU-UHFFFAOYSA-N violanthrene Chemical compound C12=C3C4=CC=C2C2=CC=CC=C2CC1=CC=C3C1=CC=C2CC3=CC=CC=C3C3=CC=C4C1=C32 JAIHDOVRCZNXDU-UHFFFAOYSA-N 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
- C09B3/00—Dyes with an anthracene nucleus condensed with one or more carbocyclic rings
- C09B3/22—Dibenzanthrones; Isodibenzanthrones
- C09B3/30—Preparation from starting materials already containing the dibenzanthrone or isodibenzanthrone nucleus
- C09B3/38—Preparation from starting materials already containing the dibenzanthrone or isodibenzanthrone nucleus by introduction of hydrocarbon or acyl residues into amino groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Publications (1)
Publication Number | Publication Date |
---|---|
DE267418C true DE267418C (en:Method) |
Family
ID=524481
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DENDAT267418D Active DE267418C (en:Method) |
Country Status (1)
Country | Link |
---|---|
DE (1) | DE267418C (en:Method) |
-
0
- DE DENDAT267418D patent/DE267418C/de active Active
Similar Documents
Publication | Publication Date | Title |
---|---|---|
DE267418C (en:Method) | ||
DE517442C (de) | Verfahren zur Darstellung von Kuepenfarbstoffen | |
DE177574C (en:Method) | ||
DE240276C (en:Method) | ||
DE235364C (en:Method) | ||
DE253714C (en:Method) | ||
DE583936C (de) | Verfahren zur Herstellung von 1íñ4-Diamino-2-aryloxyanthrachinon-3-sulfonsaeuren | |
DE555937C (de) | Verfahren zur Darstellung von hochmolekularen Kondensationsprodukten der Anthrachinonreihe | |
DE225319C (en:Method) | ||
DE108546C (en:Method) | ||
DE186597C (en:Method) | ||
DE767692C (de) | Verfahren zur Herstellung von Azofarbstoffen | |
DE632447C (de) | Verfahren zur Darstellung von Kuepenfarbstoffen | |
DE241343C (en:Method) | ||
DE280649C (en:Method) | ||
DE246581C (en:Method) | ||
DE69933C (de) | Verfahren zur Darstellung von Farbstoffen aus der Klasse der Alizarin-Cyanine. (9 | |
DE252287C (en:Method) | ||
DE172609C (en:Method) | ||
AT148470B (de) | Verfahren zur Herstellung ätzbarer, grünblauer Färbungen und Drucke auf Celluloseestern und -äthern. | |
DE227105C (en:Method) | ||
DE101372C (en:Method) | ||
DE563061C (de) | Verfahren zur Herstellung von unloeslichen Azofarbstoffen auf der Faser | |
DE203436C (en:Method) | ||
DE283724C (en:Method) |