CH470527A - Verfahren zum Färben und Bedrucken von synthetischen Textilmaterialien mit Anthrachinonfarbstoffen - Google Patents
Verfahren zum Färben und Bedrucken von synthetischen Textilmaterialien mit AnthrachinonfarbstoffenInfo
- Publication number
- CH470527A CH470527A CH516967A CH516967A CH470527A CH 470527 A CH470527 A CH 470527A CH 516967 A CH516967 A CH 516967A CH 516967 A CH516967 A CH 516967A CH 470527 A CH470527 A CH 470527A
- Authority
- CH
- Switzerland
- Prior art keywords
- sep
- triazine
- bis
- anthraquinonylamino
- dye
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims description 19
- 238000004043 dyeing Methods 0.000 title claims description 17
- 239000000463 material Substances 0.000 title claims description 9
- 229920002994 synthetic fiber Polymers 0.000 title claims description 7
- 239000004758 synthetic textile Substances 0.000 title claims description 6
- 239000001000 anthraquinone dye Substances 0.000 title description 2
- 239000000975 dye Substances 0.000 claims description 49
- -1 polyethylene terephthalates Polymers 0.000 claims description 46
- 229920000139 polyethylene terephthalate Polymers 0.000 claims description 22
- 239000004952 Polyamide Substances 0.000 claims description 12
- 229920002647 polyamide Polymers 0.000 claims description 12
- 229920002284 Cellulose triacetate Polymers 0.000 claims description 11
- NNLVGZFZQQXQNW-ADJNRHBOSA-N [(2r,3r,4s,5r,6s)-4,5-diacetyloxy-3-[(2s,3r,4s,5r,6r)-3,4,5-triacetyloxy-6-(acetyloxymethyl)oxan-2-yl]oxy-6-[(2r,3r,4s,5r,6s)-4,5,6-triacetyloxy-2-(acetyloxymethyl)oxan-3-yl]oxyoxan-2-yl]methyl acetate Chemical compound O([C@@H]1O[C@@H]([C@H]([C@H](OC(C)=O)[C@H]1OC(C)=O)O[C@H]1[C@@H]([C@@H](OC(C)=O)[C@H](OC(C)=O)[C@@H](COC(C)=O)O1)OC(C)=O)COC(=O)C)[C@@H]1[C@@H](COC(C)=O)O[C@@H](OC(C)=O)[C@H](OC(C)=O)[C@H]1OC(C)=O NNLVGZFZQQXQNW-ADJNRHBOSA-N 0.000 claims description 11
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 claims description 6
- 229920002635 polyurethane Polymers 0.000 claims description 6
- 239000004814 polyurethane Substances 0.000 claims description 6
- 125000003545 alkoxy group Chemical group 0.000 claims description 5
- 150000002431 hydrogen Chemical group 0.000 claims description 5
- 229910052739 hydrogen Inorganic materials 0.000 claims description 5
- 239000001257 hydrogen Substances 0.000 claims description 5
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 5
- 229920000728 polyester Polymers 0.000 claims description 5
- YIMQCDZDWXUDCA-UHFFFAOYSA-N [4-(hydroxymethyl)cyclohexyl]methanol Chemical compound OCC1CCC(CO)CC1 YIMQCDZDWXUDCA-UHFFFAOYSA-N 0.000 claims description 3
- 125000000217 alkyl group Chemical group 0.000 claims description 3
- 150000001875 compounds Chemical class 0.000 claims description 3
- 229910052736 halogen Inorganic materials 0.000 claims description 3
- 150000002367 halogens Chemical class 0.000 claims description 3
- 125000005530 alkylenedioxy group Chemical group 0.000 claims description 2
- 125000003118 aryl group Chemical group 0.000 claims description 2
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 2
- 125000005113 hydroxyalkoxy group Chemical group 0.000 claims description 2
- 125000002768 hydroxyalkyl group Chemical group 0.000 claims description 2
- 230000001419 dependent effect Effects 0.000 claims 3
- 239000004753 textile Substances 0.000 claims 3
- 229920002678 cellulose Polymers 0.000 claims 1
- WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 description 27
- 239000000835 fiber Substances 0.000 description 26
- 239000005020 polyethylene terephthalate Substances 0.000 description 20
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 12
- 238000009998 heat setting Methods 0.000 description 11
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 10
- 235000019445 benzyl alcohol Nutrition 0.000 description 9
- 125000000051 benzyloxy group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])O* 0.000 description 8
- 239000004744 fabric Substances 0.000 description 8
- 238000005406 washing Methods 0.000 description 8
- WRMNZCZEMHIOCP-UHFFFAOYSA-N 2-phenylethanol Chemical compound OCCC1=CC=CC=C1 WRMNZCZEMHIOCP-UHFFFAOYSA-N 0.000 description 6
- 238000001035 drying Methods 0.000 description 6
- 239000000203 mixture Substances 0.000 description 6
- 229920006306 polyurethane fiber Polymers 0.000 description 5
- 238000003756 stirring Methods 0.000 description 5
- JYEUMXHLPRZUAT-UHFFFAOYSA-N 1,2,3-triazine Chemical compound C1=CN=NN=C1 JYEUMXHLPRZUAT-UHFFFAOYSA-N 0.000 description 4
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- DYUQAZSOFZSPHD-UHFFFAOYSA-N Phenylpropyl alcohol Natural products CCC(O)C1=CC=CC=C1 DYUQAZSOFZSPHD-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 3
- 238000010409 ironing Methods 0.000 description 3
- LLLVZDVNHNWSDS-UHFFFAOYSA-N 4-methylidene-3,5-dioxabicyclo[5.2.2]undeca-1(9),7,10-triene-2,6-dione Chemical compound C1(C2=CC=C(C(=O)OC(=C)O1)C=C2)=O LLLVZDVNHNWSDS-UHFFFAOYSA-N 0.000 description 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 239000013078 crystal Substances 0.000 description 2
- 229920001971 elastomer Polymers 0.000 description 2
- 239000002657 fibrous material Substances 0.000 description 2
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
- 229950009195 phenylpropanol Drugs 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- FIDRAVVQGKNYQK-UHFFFAOYSA-N 1,2,3,4-tetrahydrotriazine Chemical compound C1NNNC=C1 FIDRAVVQGKNYQK-UHFFFAOYSA-N 0.000 description 1
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 1
- FHVDTGUDJYJELY-UHFFFAOYSA-N 6-{[2-carboxy-4,5-dihydroxy-6-(phosphanyloxy)oxan-3-yl]oxy}-4,5-dihydroxy-3-phosphanyloxane-2-carboxylic acid Chemical compound O1C(C(O)=O)C(P)C(O)C(O)C1OC1C(C(O)=O)OC(OP)C(O)C1O FHVDTGUDJYJELY-UHFFFAOYSA-N 0.000 description 1
- ZBEHHPVZYJRDGA-UHFFFAOYSA-N CCOC(C(C(C1=CC=CC=C11)=O)=C2C1=O)=CC=C2NC1=NC(OCCCC2=CC=CC=C2)=NC(OCCCC2=CC=CC=C2)=N1 Chemical compound CCOC(C(C(C1=CC=CC=C11)=O)=C2C1=O)=CC=C2NC1=NC(OCCCC2=CC=CC=C2)=NC(OCCCC2=CC=CC=C2)=N1 ZBEHHPVZYJRDGA-UHFFFAOYSA-N 0.000 description 1
- ZZSNTSAHTMGNIN-UHFFFAOYSA-N COC(C(C(C1=CC=CC=C11)=O)=C2C1=O)=CC=C2NC1=NC(OCC2=CC(Cl)=CC=C2)=NC(OCC2=CC(Cl)=CC=C2)=N1 Chemical compound COC(C(C(C1=CC=CC=C11)=O)=C2C1=O)=CC=C2NC1=NC(OCC2=CC(Cl)=CC=C2)=NC(OCC2=CC(Cl)=CC=C2)=N1 ZZSNTSAHTMGNIN-UHFFFAOYSA-N 0.000 description 1
- HQYJRJWSIQJUCQ-UHFFFAOYSA-N COC=1C=C(COC2=NC(=NC(=N2)OCC2=CC(=C(C=C2)OC)OC)NC2=CC=C(C=3C(C4=CC=CC=C4C(C23)=O)=O)OC)C=CC1OC Chemical compound COC=1C=C(COC2=NC(=NC(=N2)OCC2=CC(=C(C=C2)OC)OC)NC2=CC=C(C=3C(C4=CC=CC=C4C(C23)=O)=O)OC)C=CC1OC HQYJRJWSIQJUCQ-UHFFFAOYSA-N 0.000 description 1
- ORICASMKFDBEKI-UHFFFAOYSA-N COC=1C=C(COC2=NC(=NC(=N2)OCC2=CC(=CC=C2)OC)NC2=CC=C(C=3C(C4=CC=CC=C4C(C23)=O)=O)OC)C=CC1 Chemical compound COC=1C=C(COC2=NC(=NC(=N2)OCC2=CC(=CC=C2)OC)NC2=CC=C(C=3C(C4=CC=CC=C4C(C23)=O)=O)OC)C=CC1 ORICASMKFDBEKI-UHFFFAOYSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- 208000037062 Polyps Diseases 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 229940072056 alginate Drugs 0.000 description 1
- 235000010443 alginic acid Nutrition 0.000 description 1
- 229920000615 alginic acid Polymers 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 239000004359 castor oil Substances 0.000 description 1
- 235000019438 castor oil Nutrition 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 239000003599 detergent Substances 0.000 description 1
- GRWZHXKQBITJKP-UHFFFAOYSA-L dithionite(2-) Chemical compound [O-]S(=O)S([O-])=O GRWZHXKQBITJKP-UHFFFAOYSA-L 0.000 description 1
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 1
- 235000019253 formic acid Nutrition 0.000 description 1
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- AJDUTMFFZHIJEM-UHFFFAOYSA-N n-(9,10-dioxoanthracen-1-yl)-4-[4-[[4-[4-[(9,10-dioxoanthracen-1-yl)carbamoyl]phenyl]phenyl]diazenyl]phenyl]benzamide Chemical compound O=C1C2=CC=CC=C2C(=O)C2=C1C=CC=C2NC(=O)C(C=C1)=CC=C1C(C=C1)=CC=C1N=NC(C=C1)=CC=C1C(C=C1)=CC=C1C(=O)NC1=CC=CC2=C1C(=O)C1=CC=CC=C1C2=O AJDUTMFFZHIJEM-UHFFFAOYSA-N 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
- 125000000109 phenylethoxy group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])O* 0.000 description 1
- 229940067107 phenylethyl alcohol Drugs 0.000 description 1
- 229920002239 polyacrylonitrile Polymers 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 150000003109 potassium Chemical class 0.000 description 1
- 230000002829 reductive effect Effects 0.000 description 1
- 230000008719 thickening Effects 0.000 description 1
- 150000003918 triazines Chemical class 0.000 description 1
- 229920006307 urethane fiber Polymers 0.000 description 1
- 239000001043 yellow dye 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
- C09B62/00—Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves
- C09B62/02—Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves with the reactive group directly attached to a heterocyclic ring
- C09B62/04—Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves with the reactive group directly attached to a heterocyclic ring to a triazine ring
- C09B62/06—Anthracene dyes
-
- 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
- C09B1/36—Dyes with acylated amino groups
- C09B1/46—Dyes with acylated amino groups the acyl groups being residues of cyanuric acid or an analogous heterocyclic compound
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S8/00—Bleaching and dyeing; fluid treatment and chemical modification of textiles and fibers
- Y10S8/92—Synthetic fiber dyeing
- Y10S8/922—Polyester fiber
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DEF0049252 | 1966-05-21 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CH516967A4 CH516967A4 (en, 2012) | 1968-08-15 |
| CH470527A true CH470527A (de) | 1969-05-14 |
Family
ID=7102861
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH516967A CH470527A (de) | 1966-05-21 | 1967-04-12 | Verfahren zum Färben und Bedrucken von synthetischen Textilmaterialien mit Anthrachinonfarbstoffen |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US3488349A (en, 2012) |
| BE (1) | BE698738A (en, 2012) |
| CH (1) | CH470527A (en, 2012) |
| DE (1) | DE1619474C3 (en, 2012) |
| FR (1) | FR1523740A (en, 2012) |
| GB (1) | GB1123946A (en, 2012) |
| NL (1) | NL6706974A (en, 2012) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AR208037A1 (es) * | 1975-06-24 | 1976-11-22 | Hoechst Ag | Preparaciones de tenido estables liquidas y acuosas que contienen colorantes reactivos y de dispersion asi como su empleo para tenir o estampar materiales de fibras mixtas |
| US5961711A (en) * | 1996-12-16 | 1999-10-05 | Dainichiseika Color & Chemicals Mfg. Co., Ltd. | Pigment dispersant, pigment dispersion, and pigment dispersion for color filter |
| JP3625143B2 (ja) * | 1998-12-28 | 2005-03-02 | 大日精化工業株式会社 | 顔料の分散剤、顔料分散液及びカラーフイルター |
| IL134482A (en) | 1999-02-16 | 2002-12-01 | Dainichiseika Color Chem | Pigment dispersions and stationery and printers with the dispersions stored within them |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2742466A (en) * | 1956-04-17 | Chx n nhx c c | ||
| CA528443A (en) * | 1949-10-14 | 1956-07-31 | Ciba Limited | Water-soluble salts of derivatives of 4:4'-diaminostilbene-2:2'-disulfonic acid and process of making same |
| DE1252204B (de) * | 1960-04-20 | 1967-10-19 | Ortho Pharmaceutical Corporation, Raritan, N. J. (V. St. A.) | Verfahren zur Herstellung von 2,4-Dinitropyrrolderivaten |
| US3349089A (en) * | 1964-05-06 | 1967-10-24 | Gnii Orch Produktov I Krasitel | Triazine dyes of the anthraquinone series |
-
0
- FR FR1523740D patent/FR1523740A/fr not_active Expired
-
1966
- 1966-05-21 DE DE1619474A patent/DE1619474C3/de not_active Expired
-
1967
- 1967-04-12 CH CH516967A patent/CH470527A/de unknown
- 1967-05-12 US US637892A patent/US3488349A/en not_active Expired - Lifetime
- 1967-05-16 GB GB22699/67A patent/GB1123946A/en not_active Expired
- 1967-05-19 NL NL6706974A patent/NL6706974A/xx unknown
- 1967-05-19 BE BE698738D patent/BE698738A/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| NL6706974A (en, 2012) | 1967-11-22 |
| BE698738A (en, 2012) | 1967-11-20 |
| DE1619474A1 (de) | 1971-06-03 |
| DE1619474B2 (de) | 1974-10-17 |
| CH516967A4 (en, 2012) | 1968-08-15 |
| DE1619474C3 (de) | 1975-06-12 |
| GB1123946A (en) | 1968-08-14 |
| FR1523740A (en, 2012) | 1968-08-28 |
| US3488349A (en) | 1970-01-06 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PLZ | Patent of addition ceased |