CH129472A - Process for the production of a new dye. - Google Patents
Process for the production of a new dye.Info
- Publication number
- CH129472A CH129472A CH129472TA CH129472A CH 129472 A CH129472 A CH 129472A CH 129472T A CH129472T A CH 129472TA CH 129472 A CH129472 A CH 129472A
- Authority
- CH
- Switzerland
- Prior art keywords
- production
- dye
- new dye
- amino
- water
- Prior art date
Links
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
- C09B29/00—Monoazo dyes prepared by diazotising and coupling
- C09B29/34—Monoazo dyes prepared by diazotising and coupling from other coupling components
- C09B29/36—Monoazo dyes prepared by diazotising and coupling from other coupling components from heterocyclic compounds
- C09B29/3604—Monoazo dyes prepared by diazotising and coupling from other coupling components from heterocyclic compounds containing only a nitrogen as heteroatom
- C09B29/3647—Monoazo dyes prepared by diazotising and coupling from other coupling components from heterocyclic compounds containing only a nitrogen as heteroatom containing a five-membered ring with two nitrogen atoms as heteroatoms
- C09B29/3652—Monoazo dyes prepared by diazotising and coupling from other coupling components from heterocyclic compounds containing only a nitrogen as heteroatom containing a five-membered ring with two nitrogen atoms as heteroatoms containing a 1,2-diazoles or hydrogenated 1,2-diazoles
- C09B29/366—Monoazo dyes prepared by diazotising and coupling from other coupling components from heterocyclic compounds containing only a nitrogen as heteroatom containing a five-membered ring with two nitrogen atoms as heteroatoms containing a 1,2-diazoles or hydrogenated 1,2-diazoles containing hydroxy-1,2-diazoles, e.g. pyrazolone
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Coloring (AREA)
Description
Zusatzpatent zum Hauptpatent Nr.<B>127259.</B> Verfuhren zur Herstellung eines neuen Farbstoffes. Es wurde gefunden, dass man einen neun Farbstoff erhält, wenn man diazotierte a-Acetamino-2-amino-l-benzolsulfosäure mit dem Pyrazolonderivat, das erhalten wird aus Rohxylidin durch Sulfieren, Diazotieren, Reduzieren und Kondensieren mit Acetessig- ester, kuppelt. Der so erhaltene Farbstoff bildet ein gelbes Pulver.
Er färbt Wolle aus schwefelsaurem Bade in sehr gleich mässigen, dem Tartrazin gleichen, kräftigen Tönen. Die Färbungen sind sehr gut licht-, wasser- und alkaliecht und halten der sau ren Walke stand.
<I>Beispiel:</I> 28,4 Teile des Pyrazolonderivates, das erhalten wird aus Rohxylidin durch Sul- fieren, Diazotieren, Reduzieren und Kon densieren mit Acetessigester, werden in 150 Teilen Wasser mit 20 Teilen calcinierter Soda gelöst, mit Eis gekühlt und hierauf mit der Diazoverbindung aus 28 Teilen 4- .lcetamino-2-amino-l-benzolsulfosäure ver- setzt. Der sieh bildende Farbstoff scheidet sich teilweise aus.
Durch Zusatz von Koch salz wird die Fällung vervollständigt, dann wird möglichst neutral gestellt, filtriert und getrocknet.
Additional patent to main patent no. <B> 127259. </B> Procedure for the production of a new dye. It has been found that a nine dye is obtained when diazotized α-acetamino-2-amino-1-benzenesulfonic acid is coupled with the pyrazolone derivative obtained from crude xylidine by sulfating, diazotizing, reducing and condensing with acetoacetic ester. The dye thus obtained forms a yellow powder.
He dyes wool from a sulfuric acid bath in very even, strong tones similar to tartrazine. The dyeings are very resistant to light, water and alkali and can withstand sour fulling.
<I> Example: </I> 28.4 parts of the pyrazolone derivative, which is obtained from crude xylidine by sulphation, diazotization, reduction and condensation with acetoacetic ester, are dissolved in 150 parts of water with 20 parts of calcined soda and cooled with ice and then mixed with the diazo compound from 28 parts of 4-.lcetamino-2-amino-1-benzenesulfonic acid. The dye which forms the appearance is partially separated out.
The precipitation is completed by adding sodium chloride, then it is made as neutral as possible, filtered and dried.
Claims (1)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH129472T CH129472A (en) | 1926-12-04 | 1926-12-04 | Process for the production of a new dye. |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH127259T | 1926-12-04 | ||
CH129472T CH129472A (en) | 1926-12-04 | 1926-12-04 | Process for the production of a new dye. |
Publications (1)
Publication Number | Publication Date |
---|---|
CH129472A true CH129472A (en) | 1928-12-17 |
Family
ID=25710814
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH129472T CH129472A (en) | 1926-12-04 | 1926-12-04 | Process for the production of a new dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH129472A (en) |
-
1926
- 1926-12-04 CH CH129472T patent/CH129472A/en unknown
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