JPS6329709B2 - - Google Patents
Info
- Publication number
- JPS6329709B2 JPS6329709B2 JP54141439A JP14143979A JPS6329709B2 JP S6329709 B2 JPS6329709 B2 JP S6329709B2 JP 54141439 A JP54141439 A JP 54141439A JP 14143979 A JP14143979 A JP 14143979A JP S6329709 B2 JPS6329709 B2 JP S6329709B2
- Authority
- JP
- Japan
- Prior art keywords
- parts
- group
- dye
- acid
- formula
- 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
Links
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 4
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 2
- 229910052801 chlorine Inorganic materials 0.000 claims description 2
- 125000001309 chloro group Chemical group Cl* 0.000 claims description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 2
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 2
- 125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 claims description 2
- -1 sulfonaphthyl group Chemical group 0.000 claims description 2
- 239000000985 reactive dye Substances 0.000 claims 1
- 239000000975 dye Substances 0.000 description 15
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 10
- 230000008878 coupling Effects 0.000 description 7
- 238000010168 coupling process Methods 0.000 description 7
- 238000005859 coupling reaction Methods 0.000 description 7
- 239000000243 solution Substances 0.000 description 7
- 239000011541 reaction mixture Substances 0.000 description 5
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 5
- 235000017557 sodium bicarbonate Nutrition 0.000 description 5
- 239000002253 acid Substances 0.000 description 4
- MCSXGCZMEPXKIW-UHFFFAOYSA-N 3-hydroxy-4-[(4-methyl-2-nitrophenyl)diazenyl]-N-(3-nitrophenyl)naphthalene-2-carboxamide Chemical compound Cc1ccc(N=Nc2c(O)c(cc3ccccc23)C(=O)Nc2cccc(c2)[N+]([O-])=O)c(c1)[N+]([O-])=O MCSXGCZMEPXKIW-UHFFFAOYSA-N 0.000 description 3
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 3
- 229920000742 Cotton Polymers 0.000 description 3
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 3
- MGNCLNQXLYJVJD-UHFFFAOYSA-N cyanuric chloride Chemical compound ClC1=NC(Cl)=NC(Cl)=N1 MGNCLNQXLYJVJD-UHFFFAOYSA-N 0.000 description 3
- 238000004043 dyeing Methods 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 230000007935 neutral effect Effects 0.000 description 3
- 235000002639 sodium chloride Nutrition 0.000 description 3
- 239000011780 sodium chloride Substances 0.000 description 3
- GFPQSWFFPRQEHH-UHFFFAOYSA-N 7-aminonaphthalene-1,3,6-trisulfonic acid Chemical compound C1=C(S(O)(=O)=O)C=C2C=C(S(O)(=O)=O)C(N)=CC2=C1S(O)(=O)=O GFPQSWFFPRQEHH-UHFFFAOYSA-N 0.000 description 2
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-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
- 230000010933 acylation Effects 0.000 description 2
- 238000005917 acylation reaction Methods 0.000 description 2
- RWZYAGGXGHYGMB-UHFFFAOYSA-N anthranilic acid Chemical compound NC1=CC=CC=C1C(O)=O RWZYAGGXGHYGMB-UHFFFAOYSA-N 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 description 2
- 238000001694 spray drying Methods 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- UWPJYQYRSWYIGZ-UHFFFAOYSA-N 5-aminonaphthalene-2-sulfonic acid Chemical compound OS(=O)(=O)C1=CC=C2C(N)=CC=CC2=C1 UWPJYQYRSWYIGZ-UHFFFAOYSA-N 0.000 description 1
- KYARBIJYVGJZLB-UHFFFAOYSA-N 7-amino-4-hydroxy-2-naphthalenesulfonic acid Chemical compound OC1=CC(S(O)(=O)=O)=CC2=CC(N)=CC=C21 KYARBIJYVGJZLB-UHFFFAOYSA-N 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 239000007859 condensation product Substances 0.000 description 1
- 238000006482 condensation reaction Methods 0.000 description 1
- 150000001989 diazonium salts Chemical class 0.000 description 1
- 238000006193 diazotization reaction Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000010016 exhaust dyeing Methods 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 239000010985 leather Substances 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-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
- 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
- C09B62/085—Monoazo dyes
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
- Cosmetics (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE2847916A DE2847916C2 (de) | 1978-11-04 | 1978-11-04 | Reaktivfarbstoffe und deren Verwendung |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5565259A JPS5565259A (en) | 1980-05-16 |
| JPS6329709B2 true JPS6329709B2 (it) | 1988-06-15 |
Family
ID=6053883
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP14143979A Granted JPS5565259A (en) | 1978-11-04 | 1979-11-02 | Reactive dye |
Country Status (6)
| Country | Link |
|---|---|
| JP (1) | JPS5565259A (it) |
| CH (1) | CH641486A5 (it) |
| DE (1) | DE2847916C2 (it) |
| FR (1) | FR2440385B1 (it) |
| GB (1) | GB2036778B (it) |
| IT (1) | IT1124857B (it) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CH641197A5 (de) | 1977-12-23 | 1984-02-15 | Sandoz Ag | Reaktive monoazofarbstoffe und verfahren zu deren herstellung. |
| CH655735A5 (de) * | 1982-09-17 | 1986-05-15 | Sandoz Ag | Reaktive monoazoverbindungen. |
Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS49104923A (it) * | 1973-02-05 | 1974-10-04 | ||
| JPS5495631A (en) * | 1977-12-23 | 1979-07-28 | Sandoz Ag | Azo compound containing fiber reactive groups |
| JPS5536287A (en) * | 1978-09-01 | 1980-03-13 | Bayer Ag | Reactive azo dyestuff and utilization |
| JPS5536291A (en) * | 1978-09-05 | 1980-03-13 | Bayer Ag | Azo reactive dyestuff and production |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB908194A (en) * | 1960-08-03 | 1962-10-17 | Ici Ltd | New triazine monoazo dyestuffs |
| CH629839A5 (en) * | 1976-07-12 | 1982-05-14 | Ciba Geigy Ag | Process for preparing fibre-reactive azo dyes |
| DE2711150A1 (de) * | 1977-03-15 | 1978-09-28 | Bayer Ag | Verfahren zur herstellung von azoreaktivfarbstoffen |
| LU78485A1 (de) * | 1977-11-10 | 1979-06-13 | Ciba Geigy Ag | Reaktivfarbstoffe,deren herstellung und verwendung |
-
1978
- 1978-11-04 DE DE2847916A patent/DE2847916C2/de not_active Expired
-
1979
- 1979-10-26 FR FR7926630A patent/FR2440385B1/fr not_active Expired
- 1979-10-30 IT IT26943/79A patent/IT1124857B/it active
- 1979-10-31 CH CH977679A patent/CH641486A5/de not_active IP Right Cessation
- 1979-11-02 GB GB7937989A patent/GB2036778B/en not_active Expired
- 1979-11-02 JP JP14143979A patent/JPS5565259A/ja active Granted
Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS49104923A (it) * | 1973-02-05 | 1974-10-04 | ||
| JPS5495631A (en) * | 1977-12-23 | 1979-07-28 | Sandoz Ag | Azo compound containing fiber reactive groups |
| JPS5536287A (en) * | 1978-09-01 | 1980-03-13 | Bayer Ag | Reactive azo dyestuff and utilization |
| JPS5536291A (en) * | 1978-09-05 | 1980-03-13 | Bayer Ag | Azo reactive dyestuff and production |
Also Published As
| Publication number | Publication date |
|---|---|
| GB2036778A (en) | 1980-07-02 |
| GB2036778B (en) | 1983-08-17 |
| DE2847916C2 (de) | 1984-04-26 |
| DE2847916A1 (de) | 1980-05-22 |
| CH641486A5 (de) | 1984-02-29 |
| FR2440385A1 (fr) | 1980-05-30 |
| JPS5565259A (en) | 1980-05-16 |
| IT7926943A0 (it) | 1979-10-30 |
| FR2440385B1 (fr) | 1985-08-23 |
| IT1124857B (it) | 1986-05-14 |
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