DE1085993B - Verfahren zur Herstellung von Anthrachinonfarbstoffen - Google Patents
Verfahren zur Herstellung von AnthrachinonfarbstoffenInfo
- Publication number
- DE1085993B DE1085993B DEC16887A DEC0016887A DE1085993B DE 1085993 B DE1085993 B DE 1085993B DE C16887 A DEC16887 A DE C16887A DE C0016887 A DEC0016887 A DE C0016887A DE 1085993 B DE1085993 B DE 1085993B
- Authority
- DE
- Germany
- Prior art keywords
- preparation
- parts
- anthraquinone dyes
- dyes
- aminoanthraquinone
- 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.)
- Pending
Links
- 238000000034 method Methods 0.000 title claims description 8
- 239000001000 anthraquinone dye Substances 0.000 title claims description 3
- 238000002360 preparation method Methods 0.000 title claims description 3
- BSQLQMLFTHJVKS-UHFFFAOYSA-N 2-chloro-1,3-benzothiazole Chemical compound C1=CC=C2SC(Cl)=NC2=C1 BSQLQMLFTHJVKS-UHFFFAOYSA-N 0.000 claims description 2
- 238000009835 boiling Methods 0.000 claims description 2
- 238000009833 condensation Methods 0.000 claims description 2
- 230000005494 condensation Effects 0.000 claims description 2
- 239000002904 solvent Substances 0.000 claims description 2
- 238000010186 staining Methods 0.000 claims 1
- 239000000975 dye Substances 0.000 description 9
- 238000000859 sublimation Methods 0.000 description 4
- 230000008022 sublimation Effects 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 239000000835 fiber Substances 0.000 description 3
- 229920000728 polyester Polymers 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- 238000004043 dyeing Methods 0.000 description 2
- UHOVQNZJYSORNB-UHFFFAOYSA-N monobenzene Natural products C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 2
- LQNUZADURLCDLV-UHFFFAOYSA-N nitrobenzene Chemical compound [O-][N+](=O)C1=CC=CC=C1 LQNUZADURLCDLV-UHFFFAOYSA-N 0.000 description 2
- -1 polyethylene terephthalate Polymers 0.000 description 2
- 239000007858 starting material Substances 0.000 description 2
- 230000008961 swelling Effects 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 229920000742 Cotton Polymers 0.000 description 1
- WTDHULULXKLSOZ-UHFFFAOYSA-N Hydroxylamine hydrochloride Chemical compound Cl.ON WTDHULULXKLSOZ-UHFFFAOYSA-N 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 125000003545 alkoxy group Chemical group 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 239000007859 condensation product Substances 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 125000005843 halogen group Chemical group 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 230000020477 pH reduction Effects 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 229920000139 polyethylene terephthalate Polymers 0.000 description 1
- 239000005020 polyethylene terephthalate Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- GUEIZVNYDFNHJU-UHFFFAOYSA-N quinizarin Chemical compound O=C1C2=CC=CC=C2C(=O)C2=C1C(O)=CC=C2O GUEIZVNYDFNHJU-UHFFFAOYSA-N 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-L sulfite Chemical compound [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 description 1
- 239000002699 waste material Substances 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
- C09B1/206—Dyes with amino groups substituted by heterocyclic radicals
-
- 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
- C09B1/50—Amino-hydroxy-anthraquinones; Ethers and esters thereof
- C09B1/51—N-substituted amino-hydroxy anthraquinone
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH867791X | 1957-05-28 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE1085993B true DE1085993B (de) | 1960-07-28 |
Family
ID=4543796
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DEC16887A Pending DE1085993B (de) | 1957-05-28 | 1958-05-21 | Verfahren zur Herstellung von Anthrachinonfarbstoffen |
Country Status (5)
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1218638B (de) * | 1961-12-14 | 1966-06-08 | Kuhlmann Ets | Verfahren zur Herstellung von Farbstoffen |
| DE1226730B (de) * | 1961-08-21 | 1966-10-13 | Kuhlmann Ets | Verfahren zur Herstellung von Farbstoffen |
| DE1276258B (de) * | 1962-10-03 | 1968-08-29 | Ugine Kuhlmann | Farbstoffe fuer synthetische Fasern und Verfahren zu ihrer Herstellung |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3106438A (en) * | 1959-12-24 | 1963-10-08 | Eastman Kodak Co | Brominated 1-hydroxy-4-anilinoanthraquinone dye compounds |
| US3447886A (en) * | 1963-10-04 | 1969-06-03 | Sandoz Ag | Process for dyeing hydrophobic organic textile materials with anthraquinone dyestuffs |
| NL129223C (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) * | 1963-10-04 |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR1144813A (fr) * | 1955-04-01 | 1957-10-18 | Ciba Geigy | Nouvelles polyhydroxy-beta-acylaminoanthraquinones, leur préparation et leurs emplois |
-
0
- FR FR1193849D patent/FR1193849A/fr not_active Expired
- US US2899438D patent/US2899438A/en not_active Expired - Lifetime
-
1957
- 1957-05-28 CH CH358533D patent/CH358533A/de unknown
-
1958
- 1958-05-21 DE DEC16887A patent/DE1085993B/de active Pending
- 1958-05-28 GB GB17027/58A patent/GB867791A/en not_active Expired
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR1144813A (fr) * | 1955-04-01 | 1957-10-18 | Ciba Geigy | Nouvelles polyhydroxy-beta-acylaminoanthraquinones, leur préparation et leurs emplois |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1226730B (de) * | 1961-08-21 | 1966-10-13 | Kuhlmann Ets | Verfahren zur Herstellung von Farbstoffen |
| DE1218638B (de) * | 1961-12-14 | 1966-06-08 | Kuhlmann Ets | Verfahren zur Herstellung von Farbstoffen |
| DE1276258B (de) * | 1962-10-03 | 1968-08-29 | Ugine Kuhlmann | Farbstoffe fuer synthetische Fasern und Verfahren zu ihrer Herstellung |
Also Published As
| Publication number | Publication date |
|---|---|
| GB867791A (en) | 1961-05-10 |
| CH358533A (de) | 1961-11-30 |
| US2899438A (en) | 1959-08-11 |
| FR1193849A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1959-11-05 |
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