PL86475B1 - - Google Patents
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- Publication number
- PL86475B1 PL86475B1 PL1973163283A PL16328373A PL86475B1 PL 86475 B1 PL86475 B1 PL 86475B1 PL 1973163283 A PL1973163283 A PL 1973163283A PL 16328373 A PL16328373 A PL 16328373A PL 86475 B1 PL86475 B1 PL 86475B1
- Authority
- PL
- Poland
- Prior art keywords
- general formula
- acid
- radical
- dyes
- ammonia
- Prior art date
Links
- 239000000975 dye Substances 0.000 claims description 27
- 238000000034 method Methods 0.000 claims description 11
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 claims description 10
- 150000001875 compounds Chemical class 0.000 claims description 9
- 229910021529 ammonia Inorganic materials 0.000 claims description 5
- 125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 claims description 4
- 238000002360 preparation method Methods 0.000 claims description 4
- 238000004519 manufacturing process Methods 0.000 claims description 3
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims 2
- ULVNIJSKNRGBHX-UHFFFAOYSA-N 4-chloro-1,3,5-triazin-2-amine Chemical compound NC1=NC=NC(Cl)=N1 ULVNIJSKNRGBHX-UHFFFAOYSA-N 0.000 claims 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 claims 1
- 229910006069 SO3H Inorganic materials 0.000 claims 1
- ZFSLODLOARCGLH-UHFFFAOYSA-N isocyanuric acid Chemical compound OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 0.000 claims 1
- 239000002253 acid Substances 0.000 description 23
- 239000000203 mixture Substances 0.000 description 13
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 12
- PGEIDQFRPKWAMU-UHFFFAOYSA-N azane;2,4,6-trichloro-1,3,5-triazine Chemical compound N.ClC1=NC(Cl)=NC(Cl)=N1 PGEIDQFRPKWAMU-UHFFFAOYSA-N 0.000 description 10
- 238000004043 dyeing Methods 0.000 description 7
- 239000011541 reaction mixture Substances 0.000 description 6
- 238000005406 washing Methods 0.000 description 6
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 5
- -1 aminoazo compound Chemical class 0.000 description 5
- 239000011230 binding agent Substances 0.000 description 5
- 239000000243 solution Substances 0.000 description 5
- 238000003756 stirring Methods 0.000 description 5
- VOWZNBNDMFLQGM-UHFFFAOYSA-N 2,5-dimethylaniline Chemical compound CC1=CC=C(C)C(N)=C1 VOWZNBNDMFLQGM-UHFFFAOYSA-N 0.000 description 4
- MTJGVAJYTOXFJH-UHFFFAOYSA-N 3-aminonaphthalene-1,5-disulfonic acid Chemical compound C1=CC=C(S(O)(=O)=O)C2=CC(N)=CC(S(O)(=O)=O)=C21 MTJGVAJYTOXFJH-UHFFFAOYSA-N 0.000 description 4
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 4
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 4
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 4
- MGNCLNQXLYJVJD-UHFFFAOYSA-N cyanuric chloride Chemical compound ClC1=NC(Cl)=NC(Cl)=N1 MGNCLNQXLYJVJD-UHFFFAOYSA-N 0.000 description 4
- 239000000835 fiber Substances 0.000 description 4
- LPXPTNMVRIOKMN-UHFFFAOYSA-M sodium nitrite Chemical compound [Na+].[O-]N=O LPXPTNMVRIOKMN-UHFFFAOYSA-M 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- WXWCDTXEKCVRRO-UHFFFAOYSA-N para-Cresidine Chemical compound COC1=CC=C(C)C=C1N WXWCDTXEKCVRRO-UHFFFAOYSA-N 0.000 description 3
- 239000004753 textile Substances 0.000 description 3
- JJYPMNFTHPTTDI-UHFFFAOYSA-N 3-methylaniline Chemical compound CC1=CC=CC(N)=C1 JJYPMNFTHPTTDI-UHFFFAOYSA-N 0.000 description 2
- CYJJLCDCWVZEDZ-UHFFFAOYSA-N 8-aminonaphthalene-1-sulfonic acid Chemical compound C1=CC(S(O)(=O)=O)=C2C(N)=CC=CC2=C1 CYJJLCDCWVZEDZ-UHFFFAOYSA-N 0.000 description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 239000007844 bleaching agent Substances 0.000 description 2
- 230000008878 coupling Effects 0.000 description 2
- 238000010168 coupling process Methods 0.000 description 2
- 238000005859 coupling reaction Methods 0.000 description 2
- NCBZRJODKRCREW-UHFFFAOYSA-N m-anisidine Chemical compound COC1=CC=CC(N)=C1 NCBZRJODKRCREW-UHFFFAOYSA-N 0.000 description 2
- 239000002609 medium Substances 0.000 description 2
- LNOPIUAQISRISI-UHFFFAOYSA-N n'-hydroxy-2-propan-2-ylsulfonylethanimidamide Chemical compound CC(C)S(=O)(=O)CC(N)=NO LNOPIUAQISRISI-UHFFFAOYSA-N 0.000 description 2
- 239000002244 precipitate Substances 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 239000001632 sodium acetate Substances 0.000 description 2
- 235000017281 sodium acetate Nutrition 0.000 description 2
- 229910000029 sodium carbonate Inorganic materials 0.000 description 2
- 239000011780 sodium chloride Substances 0.000 description 2
- 235000010288 sodium nitrite Nutrition 0.000 description 2
- ZNXSFVXZQBETRJ-UHFFFAOYSA-N (3-aminophenyl)urea Chemical compound NC(=O)NC1=CC=CC(N)=C1 ZNXSFVXZQBETRJ-UHFFFAOYSA-N 0.000 description 1
- JKAPWXKZLYJQJJ-UHFFFAOYSA-N 2,4-dichloro-6-methoxy-1,3,5-triazine Chemical compound COC1=NC(Cl)=NC(Cl)=N1 JKAPWXKZLYJQJJ-UHFFFAOYSA-N 0.000 description 1
- NAZDVUBIEPVUKE-UHFFFAOYSA-N 2,5-dimethoxyaniline Chemical compound COC1=CC=C(OC)C(N)=C1 NAZDVUBIEPVUKE-UHFFFAOYSA-N 0.000 description 1
- DVLOIGSXYNRCNP-UHFFFAOYSA-N 2-amino-1h-naphthalene-1,2-disulfonic acid Chemical compound C1=CC=C2C(S(O)(=O)=O)C(N)(S(O)(=O)=O)C=CC2=C1 DVLOIGSXYNRCNP-UHFFFAOYSA-N 0.000 description 1
- MCXKSWWEONHVOU-UHFFFAOYSA-N 3-aminonaphthalene-1,5-disulfonic acid;3-aminonaphthalene-2,7-disulfonic acid Chemical compound C1=CC=C(S(O)(=O)=O)C2=CC(N)=CC(S(O)(=O)=O)=C21.C1=C(S(O)(=O)=O)C=C2C=C(S(O)(=O)=O)C(N)=CC2=C1 MCXKSWWEONHVOU-UHFFFAOYSA-N 0.000 description 1
- WWOFHIDPAUSTAO-UHFFFAOYSA-N 3-aminonaphthalene-2,6-disulfonic acid Chemical compound OS(=O)(=O)C1=CC=C2C=C(S(O)(=O)=O)C(N)=CC2=C1 WWOFHIDPAUSTAO-UHFFFAOYSA-N 0.000 description 1
- MCLXKFUCPVGZEN-UHFFFAOYSA-N 4,6-dichloro-1,3,5-triazin-2-amine Chemical compound NC1=NC(Cl)=NC(Cl)=N1 MCLXKFUCPVGZEN-UHFFFAOYSA-N 0.000 description 1
- KZCSUEYBKAPKNH-UHFFFAOYSA-N 6-aminonaphthalene-1,3-disulfonic acid Chemical compound OS(=O)(=O)C1=CC(S(O)(=O)=O)=CC2=CC(N)=CC=C21 KZCSUEYBKAPKNH-UHFFFAOYSA-N 0.000 description 1
- FYVOTMMSGKWFPK-UHFFFAOYSA-N 7-aminonaphthalene-1-sulfonic acid Chemical compound C1=CC=C(S(O)(=O)=O)C2=CC(N)=CC=C21 FYVOTMMSGKWFPK-UHFFFAOYSA-N 0.000 description 1
- QEZZCWMQXHXAFG-UHFFFAOYSA-N 8-aminonaphthalene-2-sulfonic acid Chemical compound C1=C(S(O)(=O)=O)C=C2C(N)=CC=CC2=C1 QEZZCWMQXHXAFG-UHFFFAOYSA-N 0.000 description 1
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 1
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical compound OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
- IOVCWXUNBOPUCH-UHFFFAOYSA-N Nitrous acid Chemical compound ON=O IOVCWXUNBOPUCH-UHFFFAOYSA-N 0.000 description 1
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 1
- 229920000297 Rayon Polymers 0.000 description 1
- 239000004115 Sodium Silicate Substances 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 235000011114 ammonium hydroxide Nutrition 0.000 description 1
- 239000012736 aqueous medium Substances 0.000 description 1
- 125000000751 azo group Chemical group [*]N=N[*] 0.000 description 1
- 238000004061 bleaching Methods 0.000 description 1
- 239000012267 brine Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 239000012954 diazonium Substances 0.000 description 1
- 150000001989 diazonium salts Chemical class 0.000 description 1
- 238000006193 diazotization reaction Methods 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 1
- 229910000041 hydrogen chloride Inorganic materials 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- PEMGGJDINLGTON-UHFFFAOYSA-N n-(3-aminophenyl)acetamide Chemical compound CC(=O)NC1=CC=CC(N)=C1 PEMGGJDINLGTON-UHFFFAOYSA-N 0.000 description 1
- 125000001624 naphthyl group Chemical group 0.000 description 1
- 229910017604 nitric acid Inorganic materials 0.000 description 1
- VMPITZXILSNTON-UHFFFAOYSA-N o-anisidine Chemical compound COC1=CC=CC=C1N VMPITZXILSNTON-UHFFFAOYSA-N 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 239000000985 reactive dye Substances 0.000 description 1
- 239000004627 regenerated cellulose Substances 0.000 description 1
- 229910052911 sodium silicate Inorganic materials 0.000 description 1
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000001694 spray drying Methods 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000007858 starting material 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
- C09B62/08—Azo dyes
- C09B62/09—Disazo or polyazo 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
- C09B31/00—Disazo and polyazo dyes of the type A->B->C, A->B->C->D, or the like, prepared by diazotising and coupling
- C09B31/02—Disazo dyes
- C09B31/04—Disazo dyes from a coupling component "C" containing a directive amino group
- C09B31/053—Amino naphthalenes
- C09B31/057—Amino naphthalenes containing acid groups, e.g. —CO2H, —SO3H, —PO3H2, —OSO3H, —OPO2H2; Salts thereof
-
- 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
- Y10S534/00—Organic compounds -- part of the class 532-570 series
- Y10S534/01—Mixtures of azo compounds
-
- 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
- Y10S8/916—Natural fiber dyeing
- Y10S8/918—Cellulose textile
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB2774472A GB1386625A (en) | 1972-06-14 | 1972-06-14 | Reactive disazo dyestuffs |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| PL86475B1 true PL86475B1 (en, 2012) | 1976-05-31 |
Family
ID=10264560
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PL1973163283A PL86475B1 (en, 2012) | 1972-06-14 | 1973-06-12 |
Country Status (20)
| Country | Link |
|---|---|
| US (1) | US3950128A (en, 2012) |
| JP (1) | JPS4992109A (en, 2012) |
| AR (1) | AR197236A1 (en, 2012) |
| AU (1) | AU461946B2 (en, 2012) |
| BE (1) | BE800737A (en, 2012) |
| BR (1) | BR7304365D0 (en, 2012) |
| CH (1) | CH578037A5 (en, 2012) |
| CS (2) | CS167388B2 (en, 2012) |
| DD (1) | DD104312A5 (en, 2012) |
| DE (1) | DE2329135C3 (en, 2012) |
| ES (2) | ES415899A1 (en, 2012) |
| FR (1) | FR2187861B1 (en, 2012) |
| GB (1) | GB1386625A (en, 2012) |
| IT (1) | IT987758B (en, 2012) |
| NL (1) | NL7308264A (en, 2012) |
| OA (1) | OA04421A (en, 2012) |
| PH (1) | PH10216A (en, 2012) |
| PL (1) | PL86475B1 (en, 2012) |
| TR (1) | TR17227A (en, 2012) |
| ZA (1) | ZA733278B (en, 2012) |
Families Citing this family (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| LU78420A1 (de) * | 1977-10-31 | 1979-06-01 | Ciba Geigy Ag | Farbstoffe,deren herstellung und verwendung |
| JPS56155250A (en) | 1980-04-10 | 1981-12-01 | Nippon Kayaku Co Ltd | Reactive dis-azo compound, production thereof and dyeing method employing the same |
| JPS57121058A (en) * | 1981-01-21 | 1982-07-28 | Sumitomo Chem Co Ltd | Bifunctional disazo reactive dye |
| JPS58204052A (ja) * | 1982-05-21 | 1983-11-28 | Sumitomo Chem Co Ltd | ジスアゾ化合物およびそれを用いる有機材料の染色法 |
| DE3300373A1 (de) * | 1983-01-07 | 1984-07-12 | Basf Ag, 6700 Ludwigshafen | Reaktivfarbstoffe |
| DE3479589D1 (en) * | 1983-11-10 | 1989-10-05 | Ciba Geigy Ag | Process for the preparation of reactive dyes |
| DE3517366A1 (de) * | 1985-05-14 | 1986-11-20 | Basf Ag, 6700 Ludwigshafen | Reaktivfarbstoffe |
| JPS63278972A (ja) * | 1987-05-11 | 1988-11-16 | Mitsubishi Kasei Corp | 水溶性ジスアゾ色素 |
| DE3724931A1 (de) * | 1987-07-28 | 1989-02-09 | Hoechst Ag | Wasserloesliche disazoverbindungen, verfahren zu ihrer herstellung und ihre verwendung als farbstoffe |
| TWI525156B (zh) * | 2011-04-12 | 2016-03-11 | 臺灣永光化學工業股份有限公司 | 反應性染料 |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3050515A (en) * | 1958-03-24 | 1962-08-21 | Ciba Geigy Corp | Water-soluble disazo-dyestuffs |
| US3165506A (en) * | 1960-08-12 | 1965-01-12 | Ciba Geigy Corp | Disazo dyestuffs containing a trisulfonate diazo component |
| AT238342B (de) * | 1961-11-06 | 1965-02-10 | Ciba Geigy | Verfahren zur Herstellung neuer Disazofarbstoffe |
-
1972
- 1972-06-14 GB GB2774472A patent/GB1386625A/en not_active Expired
-
1973
- 1973-05-11 US US05/359,542 patent/US3950128A/en not_active Expired - Lifetime
- 1973-05-15 ZA ZA733278A patent/ZA733278B/xx unknown
- 1973-05-17 AU AU55818/73A patent/AU461946B2/en not_active Expired
- 1973-05-21 IT IT24350/73A patent/IT987758B/it active
- 1973-05-25 TR TR17227A patent/TR17227A/xx unknown
- 1973-06-07 DE DE2329135A patent/DE2329135C3/de not_active Expired
- 1973-06-08 BE BE132122A patent/BE800737A/xx unknown
- 1973-06-11 CS CS3621A patent/CS167388B2/cs unknown
- 1973-06-11 CS CS4196A patent/CS167387B2/cs unknown
- 1973-06-11 PH PH14718A patent/PH10216A/en unknown
- 1973-06-12 DD DD171479A patent/DD104312A5/xx unknown
- 1973-06-12 BR BR4365/73A patent/BR7304365D0/pt unknown
- 1973-06-12 PL PL1973163283A patent/PL86475B1/pl unknown
- 1973-06-13 OA OA54931A patent/OA04421A/xx unknown
- 1973-06-13 FR FR7321472A patent/FR2187861B1/fr not_active Expired
- 1973-06-14 ES ES415899A patent/ES415899A1/es not_active Expired
- 1973-06-14 JP JP48067315A patent/JPS4992109A/ja active Pending
- 1973-06-14 ES ES415900A patent/ES415900A1/es not_active Expired
- 1973-06-14 AR AR248574A patent/AR197236A1/es active
- 1973-06-14 NL NL7308264A patent/NL7308264A/xx unknown
- 1973-06-14 CH CH862673A patent/CH578037A5/xx not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| FR2187861A1 (en, 2012) | 1974-01-18 |
| DE2329135B2 (de) | 1977-08-18 |
| ZA733278B (en) | 1974-06-26 |
| IT987758B (it) | 1975-03-20 |
| ES415899A1 (es) | 1976-02-01 |
| ES415900A1 (es) | 1976-02-01 |
| BE800737A (fr) | 1973-12-10 |
| DE2329135A1 (de) | 1974-01-03 |
| BR7304365D0 (pt) | 1974-08-29 |
| CS167388B2 (en, 2012) | 1976-04-29 |
| FR2187861B1 (en, 2012) | 1975-08-22 |
| AU5581873A (en) | 1974-11-21 |
| CS167387B2 (en, 2012) | 1976-04-29 |
| CH578037A5 (en, 2012) | 1976-07-30 |
| DE2329135C3 (de) | 1978-04-20 |
| OA04421A (fr) | 1980-02-29 |
| AU461946B2 (en) | 1975-06-12 |
| PH10216A (en) | 1976-09-29 |
| AR197236A1 (es) | 1974-03-22 |
| JPS4992109A (en, 2012) | 1974-09-03 |
| TR17227A (tr) | 1976-08-03 |
| NL7308264A (en, 2012) | 1973-12-18 |
| DD104312A5 (en, 2012) | 1974-03-05 |
| GB1386625A (en) | 1975-03-12 |
| US3950128A (en) | 1976-04-13 |
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