ES416264A1 - Procedure for dying or stamping organic materials with azoic developing colorants. (Machine-translation by Google Translate, not legally binding) - Google Patents
Procedure for dying or stamping organic materials with azoic developing colorants. (Machine-translation by Google Translate, not legally binding)Info
- Publication number
- ES416264A1 ES416264A1 ES416264A ES416264A ES416264A1 ES 416264 A1 ES416264 A1 ES 416264A1 ES 416264 A ES416264 A ES 416264A ES 416264 A ES416264 A ES 416264A ES 416264 A1 ES416264 A1 ES 416264A1
- Authority
- ES
- Spain
- Prior art keywords
- group
- formula
- radical
- see formula
- optionally substituted
- 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
- 239000011368 organic material Substances 0.000 title abstract 4
- 238000000034 method Methods 0.000 title abstract 2
- 239000003086 colorant Substances 0.000 title 1
- -1 heterocyclic radical Chemical class 0.000 abstract 8
- 125000003277 amino group Chemical group 0.000 abstract 4
- 229910052739 hydrogen Inorganic materials 0.000 abstract 4
- 239000001257 hydrogen Substances 0.000 abstract 4
- 125000004435 hydrogen atom Chemical class [H]* 0.000 abstract 4
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 abstract 3
- 125000005843 halogen group Chemical group 0.000 abstract 3
- 150000003254 radicals Chemical class 0.000 abstract 3
- 125000000547 substituted alkyl group Chemical group 0.000 abstract 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 2
- 230000008878 coupling Effects 0.000 abstract 2
- 238000010168 coupling process Methods 0.000 abstract 2
- 238000005859 coupling reaction Methods 0.000 abstract 2
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 2
- 125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 abstract 2
- 125000003107 substituted aryl group Chemical group 0.000 abstract 2
- 125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 abstract 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
- 125000004442 acylamino group Chemical group 0.000 abstract 1
- 125000004945 acylaminoalkyl group Chemical group 0.000 abstract 1
- 125000004453 alkoxycarbonyl group Chemical group 0.000 abstract 1
- 125000005079 alkoxycarbonylmethyl group Chemical group 0.000 abstract 1
- 125000004448 alkyl carbonyl group Chemical group 0.000 abstract 1
- 125000002947 alkylene group Chemical group 0.000 abstract 1
- 125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 abstract 1
- 125000005129 aryl carbonyl group Chemical group 0.000 abstract 1
- 125000003118 aryl group Chemical group 0.000 abstract 1
- 125000005161 aryl oxy carbonyl group Chemical group 0.000 abstract 1
- 239000000987 azo dye Substances 0.000 abstract 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 1
- 238000006243 chemical reaction Methods 0.000 abstract 1
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 1
- 238000004043 dyeing Methods 0.000 abstract 1
- 125000005842 heteroatom Chemical group 0.000 abstract 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 1
- 125000004029 hydroxymethyl group Chemical group [H]OC([H])([H])* 0.000 abstract 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 1
- 229910052757 nitrogen Inorganic materials 0.000 abstract 1
- 125000000018 nitroso group Chemical group N(=O)* 0.000 abstract 1
- 125000004430 oxygen atom Chemical group O* 0.000 abstract 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 1
- UBQKCCHYAOITMY-UHFFFAOYSA-N pyridin-2-ol Chemical group OC1=CC=CC=N1 UBQKCCHYAOITMY-UHFFFAOYSA-N 0.000 abstract 1
- 125000004964 sulfoalkyl group Chemical group 0.000 abstract 1
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 abstract 1
Landscapes
- Pyridine Compounds (AREA)
Abstract
Procedure for dyeing or printing organic materials with developmental azo dyes, in which diazo salts and coupling components are brought onto the organic material to be dyed or stamped successively or simultaneously and are coupled together, characterized in that as components For coupling the diazo components, in the dye-forming reaction in the same organic material to be stained, at least one of the following formulas is selected: **(See formula)** in which R1 means hydrogen, an optionally substituted alkyl group, a fibroreactive acylaminoalkyl group, an optionally substituted aryl radical, a heterocyclic radical, an alkylene radical, which links the radical of the formula (1) with another heterocyclic radical of the same class, an optionally N-monosubstituted or N-disubstituted amino group, R2 means hydrogen, an optionally substituted alkyl group, cycloalkyl, cyano, nitro, nitroso, H2N, an acylamino group that eventually shows monoreactive groups, an alkylcarbonyl, arylcarbonyl or sulfonyl group, an aminosulfonyl group, an alkoxycarbonyl radical or aryloxycarbonyl, an aminocarbonyl group, a halogen atom, a sulfoalkyl group, an acylaminomethyl group, in which the acyl radical corresponds to the formula -CO-RX, where R is an alkyl ene group and X a halogen atom, a quaternized amino group or a sulfo group, or a group of the formulas **(See formula)** in which the two groups -C0- or -SO2- are linked in a neighboring position to a 6-membered aromatic ring, the sulfo or carboxyl group, a quaternized amino group or a group of the formula **(See formula)** in which the hydrogen atom is part of a 5- or 6-membered ring, which may still contain other heteroatoms, such as nitrogen or oxygen atoms, R3 signifies hydrogen, an optionally substituted alkyl group, an optionally substituted aryl radical, a heterocyclic radical, the cyano group, an alkoxycarbonyl or aryloxycarbonyl radical, an aminocarbonyl group, an alkoxycarbonylmethyl or aryloxycarbonylmethyl radical, a cyanomethyl group, a group of acylomethyl, an aminocarbonyl group, the carboxyl group or the hydroxymethyl group, or those of formula (2) **(See formula)** in which R2 and R3 have the meanings indicated in the explanation of formula (1) and X means a group - (CH2), where n is 2 or 3 or a radical of the formula **(See formula)** and of the formula (3) **(See formula)** in which R1 has the significance indicated in the explanation of formula (I), and R2 and R3 together with the carbon atoms of the pyridone ring, to which they are attached, form a 5- or 6-membered ring, for example composed of the formulas **(See formula)** in which R1 has the significance indicated in the explanation of formula (I), and H indicates on the ring the fully hydrogenated state of the respective ring, as well as those of formula (4) **(See formula)** in which X means the hydroxyl or amino group e Y means a hydrogen or halogen atom. (Machine-translation by Google Translate, not legally binding)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE2231245A DE2231245C3 (en) | 1972-06-26 | 1972-06-26 | Process for dyeing and printing cellulose, linen, wool, silk, polyamides or leather with development mono- or disazo dyes |
| CH781773A CH564121A (en) | 1972-06-26 | 1973-05-29 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES416264A1 true ES416264A1 (en) | 1976-06-01 |
Family
ID=25702272
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES416264A Expired ES416264A1 (en) | 1972-06-26 | 1973-06-25 | Procedure for dying or stamping organic materials with azoic developing colorants. (Machine-translation by Google Translate, not legally binding) |
Country Status (2)
| Country | Link |
|---|---|
| ES (1) | ES416264A1 (en) |
| IT (1) | IT985786B (en) |
-
1973
- 1973-06-25 ES ES416264A patent/ES416264A1/en not_active Expired
- 1973-06-26 IT IT5103573A patent/IT985786B/en active
Also Published As
| Publication number | Publication date |
|---|---|
| IT985786B (en) | 1974-12-20 |
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