ES320540A1 - New reactive dyestuffs containing a triazine residue and processes for their manufacture and use - Google Patents
New reactive dyestuffs containing a triazine residue and processes for their manufacture and useInfo
- Publication number
- ES320540A1 ES320540A1 ES0320540A ES320540A ES320540A1 ES 320540 A1 ES320540 A1 ES 320540A1 ES 0320540 A ES0320540 A ES 0320540A ES 320540 A ES320540 A ES 320540A ES 320540 A1 ES320540 A1 ES 320540A1
- Authority
- ES
- Spain
- Prior art keywords
- amino
- sulphonic acid
- cyanuric chloride
- manufacture
- processes
- 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
- JYEUMXHLPRZUAT-UHFFFAOYSA-N 1,2,3-triazine Chemical group C1=CN=NN=C1 JYEUMXHLPRZUAT-UHFFFAOYSA-N 0.000 title 1
- 238000004519 manufacturing process Methods 0.000 title 1
- 238000000034 method Methods 0.000 title 1
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 abstract 3
- MGNCLNQXLYJVJD-UHFFFAOYSA-N cyanuric chloride Chemical compound ClC1=NC(Cl)=NC(Cl)=N1 MGNCLNQXLYJVJD-UHFFFAOYSA-N 0.000 abstract 3
- QJGHJWKPZQIOSN-UHFFFAOYSA-N (4-aminophenyl)methanesulfonic acid Chemical compound NC1=CC=C(CS(O)(=O)=O)C=C1 QJGHJWKPZQIOSN-UHFFFAOYSA-N 0.000 abstract 2
- 150000001412 amines Chemical class 0.000 abstract 2
- 239000000975 dye Substances 0.000 abstract 2
- 239000000543 intermediate Substances 0.000 abstract 2
- JVMSQRAXNZPDHF-UHFFFAOYSA-N 2,4-diaminobenzenesulfonic acid Chemical compound NC1=CC=C(S(O)(=O)=O)C(N)=C1 JVMSQRAXNZPDHF-UHFFFAOYSA-N 0.000 abstract 1
- HRXZRAXKKNUKRF-UHFFFAOYSA-N 4-ethylaniline Chemical compound CCC1=CC=C(N)C=C1 HRXZRAXKKNUKRF-UHFFFAOYSA-N 0.000 abstract 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 abstract 1
- 125000002947 alkylene group Chemical group 0.000 abstract 1
- 125000003277 amino group Chemical group 0.000 abstract 1
- 125000003118 aryl group Chemical group 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 150000002790 naphthalenes Chemical class 0.000 abstract 1
- 125000004430 oxygen atom Chemical group O* 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-N sulfonic acid Chemical group OS(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-N 0.000 abstract 1
- 150000003918 triazines Chemical class 0.000 abstract 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Abstract
Triazine derivatives are obtained by reacting cyanuric chloride with a dyestuff intermediate containing an acylatable amino group and with an amine of the benzene or naphthalene series which contains a sulphato or sulphonic acid group in an alkylene chain bound either directly or through an O atom to the aromatic nucleus of the amine or the water-soluble salts thereof. Examples are given in which 3- or 4-aminobenzyl sulphonic acid, 3-amino-4-methyl- or -methoxy-benzyl sulphonic acid or 4-amino-#- sulphatoethoxybenzene and 3-amino-4-sulphoaniline are reacted with cyanuric chloride, and in which 3- or 4-aminobenzyl sulphonic acid, or 4-amino-phenylethane-#-sulphonic acid and 2- amino-5-hydroxy-naphthalene-7-sulphonic acid are reacted with cyanuric chloride. The compounds are useful as dyestuff intermediates (see Division C4).
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH1609564A CH460204A (en) | 1964-12-11 | 1964-12-11 | Process for the production of new dyes |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES320540A1 true ES320540A1 (en) | 1966-06-01 |
Family
ID=4414414
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES0320540A Expired ES320540A1 (en) | 1964-12-11 | 1965-12-09 | New reactive dyestuffs containing a triazine residue and processes for their manufacture and use |
Country Status (6)
| Country | Link |
|---|---|
| BE (1) | BE673588A (en) |
| CH (1) | CH460204A (en) |
| DE (1) | DE1544455A1 (en) |
| ES (1) | ES320540A1 (en) |
| FR (1) | FR1464923A (en) |
| GB (1) | GB1127163A (en) |
-
1964
- 1964-12-11 CH CH1609564A patent/CH460204A/en unknown
-
1965
- 1965-11-30 FR FR40333A patent/FR1464923A/en not_active Expired
- 1965-12-03 DE DE19651544455 patent/DE1544455A1/en active Pending
- 1965-12-08 GB GB5206465A patent/GB1127163A/en not_active Expired
- 1965-12-09 ES ES0320540A patent/ES320540A1/en not_active Expired
- 1965-12-10 BE BE673588A patent/BE673588A/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| GB1127163A (en) | 1968-09-11 |
| CH460204A (en) | 1968-07-31 |
| BE673588A (en) | 1966-06-10 |
| FR1464923A (en) | 1967-01-06 |
| DE1544455A1 (en) | 1970-05-14 |
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