AT76018B - Process for the preparation of blue tetrakisazo dyes. - Google Patents
Process for the preparation of blue tetrakisazo dyes.Info
- Publication number
- AT76018B AT76018B AT76018DA AT76018B AT 76018 B AT76018 B AT 76018B AT 76018D A AT76018D A AT 76018DA AT 76018 B AT76018 B AT 76018B
- Authority
- AT
- Austria
- Prior art keywords
- preparation
- blue
- tetrakisazo dyes
- acid
- azo
- Prior art date
Links
- 239000000975 dye Substances 0.000 title claims description 7
- 238000000034 method Methods 0.000 title claims description 5
- 238000002360 preparation method Methods 0.000 title claims description 4
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 claims description 4
- 239000002253 acid Substances 0.000 claims description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims 3
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 claims 2
- 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 claims 1
- 239000013067 intermediate product Substances 0.000 claims 1
- 230000004048 modification Effects 0.000 claims 1
- 238000012986 modification Methods 0.000 claims 1
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- KYARBIJYVGJZLB-UHFFFAOYSA-N 7-amino-4-hydroxy-2-naphthalenesulfonic acid Chemical group OC1=CC(S(O)(=O)=O)=CC2=CC(N)=CC=C21 KYARBIJYVGJZLB-UHFFFAOYSA-N 0.000 description 1
- MYLBTCQBKAKUTJ-UHFFFAOYSA-N 7-methyl-6,8-bis(methylsulfanyl)pyrrolo[1,2-a]pyrazine Chemical compound C1=CN=CC2=C(SC)C(C)=C(SC)N21 MYLBTCQBKAKUTJ-UHFFFAOYSA-N 0.000 description 1
- 101100243951 Caenorhabditis elegans pie-1 gene Proteins 0.000 description 1
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 230000008878 coupling Effects 0.000 description 1
- 238000010168 coupling process Methods 0.000 description 1
- 238000005859 coupling reaction Methods 0.000 description 1
- 238000004043 dyeing Methods 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Coloring (AREA)
Description
<Desc/Clms Page number 1>
Verfahren zur Darstellung blauer Tetrakisazofarbstoffe.
Durch das Stammpatent Nr. 72639 wurde geschützt ein Verfahren zur Darstellung von Tetrakisazofarbstoffen entsprechend dem Schema :
2-Aminonaphthalin-4,8-disulfosäure-azo-MI-azo-MII-azo-MIII-azo-Resorcin, wobei unter M, M"und je eine diazotierbare Mittelkomponente zu verstehen ist.
Diese Farbstoffe werden auf der Faser mit Formaldehyd nachbehandelt und liefern so wasch-und lichtechte blaue Färbungen.
Es wurde nun gefunden, dass, wenn in obigem Schema MIII 2-Amino-5-naphthol- 7-sulfonsäure bedeutet, statt der 2-Aminonaphthalin-4. 8-disulfosäure mit ähnlichem Erfolge auch andere Aminoarylsulfosäuren an erster Stelle verwendet werden können.
Bei s pie 1 : Der nach dem Verfahren der Patentschrift Nr. 7092 dargestellte tertiäre TrisazofarbstoffMetanilsäure-azo-1-Naphthylamino-azo-1-Naphthylamin-6-sulfosäure-azo-2 Amino-5-oxynaphtalin-7-sulfosäure wird in heissemWasser gelöst und nach dem Abkühlen auf 5@
EMI1.1
in eine mit überschüssiger Soda versetzte Resorcin ! ösnng einlaufen und salzt nach beendeter Kupplung den Farbstoff aus.
**WARNUNG** Ende DESC Feld kannt Anfang CLMS uberlappen**.
<Desc / Clms Page number 1>
Process for the preparation of blue tetrakisazo dyes.
A process for the preparation of tetrakisazo dyes according to the scheme was protected by the parent patent No. 72639:
2-aminonaphthalene-4,8-disulfonic acid-azo-MI-azo-MII-azo-MIII-azo-resorcinol, where M, M "and a diazotizable middle component are to be understood.
These dyes are aftertreated on the fiber with formaldehyde and thus provide washable and lightfast blue dyeings.
It has now been found that if MIII in the above scheme is 2-amino-5-naphthol-7-sulfonic acid, instead of 2-aminonaphthalene-4. 8-disulfonic acid other aminoarylsulfonic acids can also be used in the first place with similar success.
At pie 1: The tertiary trisazo dye, metanilic acid-azo-1-naphthylamino-azo-1-naphthylamine-6-sulfonic acid-azo-2-amino-5-oxynaphthalene-7-sulfonic acid, prepared according to the method of patent specification No. 7092 is dissolved in hot water and after cooling down to 5 @
EMI1.1
in a resorcinol mixed with excess soda! Run in slowly and, after coupling is complete, salt out the dye.
** WARNING ** End of DESC field may overlap beginning of CLMS **.
Claims (1)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE72639X | 1914-10-29 | ||
| DE76018X | 1915-10-22 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AT76018B true AT76018B (en) | 1919-04-10 |
Family
ID=25749617
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AT76018D AT76018B (en) | 1914-10-29 | 1916-09-18 | Process for the preparation of blue tetrakisazo dyes. |
Country Status (1)
| Country | Link |
|---|---|
| AT (1) | AT76018B (en) |
-
1916
- 1916-09-18 AT AT76018D patent/AT76018B/en active
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