CH128909A - Process for the production of a new dye. - Google Patents
Process for the production of a new dye.Info
- Publication number
- CH128909A CH128909A CH128909TA CH128909A CH 128909 A CH128909 A CH 128909A CH 128909T A CH128909T A CH 128909TA CH 128909 A CH128909 A CH 128909A
- Authority
- CH
- Switzerland
- Prior art keywords
- dye
- production
- new dye
- sulfophenyl
- benzoylamino
- 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
<B>Zusatzpatent</B> zum Hauptpatent Nr. 127259. Verfahren zur Herstellung eines neuen Farbstoffes. Es wurde gefunden, dass man einen neuen Farbstoff erhält, wenn man diazotierte 4- Benzoylamino - 2 - amino -1- benzolsulfosäure mit 1-p-Sulf ophenyl -3- methyl -5- pyrazolon kuppelt. Der so erhaltene Farbstoff bil det ein gelbes Pulver.
Er färbt Wolle aus schwefelsaurem Bade in sehr gleichmässigen, rotgelben Tönen, Die Färbungen sind sehr gut licht-, wasser-, wasch- und alkaliechtund halten der sauren Walke stand. <I>Beispiel:</I> <B>25,5</B> Teile 1-p-Sulfophenyl-3-methyl-5-pyr- azolonwerden in 150 Teilen Wasser mit 20 Tei len calciniertenSoda gelöst, mitEisgekühltund hierauf mit der Diazoverbindung aus<B>29,2</B> Tei len 4 - Benzoylamino -2- amino -1- benzolsulfo- säure versetzt.
Der sich bildende Farbstoff scheidet sich teilweise aus. Durch Zusatz von Kochsalz wird die Fällung vervollständigt, dann wird möglichst neutral gestellt, fil triert und getrocknet.
<B> Additional patent </B> to main patent no. 127259. Process for the production of a new dye. It has been found that a new dye is obtained if diazotized 4-benzoylamino-2-amino-1-benzenesulfonic acid is coupled with 1-p-sulfophenyl -3-methyl -5-pyrazolone. The dye thus obtained forms a yellow powder.
He dyes wool from sulfuric acid bath in very even, red-yellow tones. The dyes are very light, water, wash and alkali fast and withstand acid fulling. <I> Example: </I> <B> 25.5 </B> parts of 1-p-sulfophenyl-3-methyl-5-pyrazolone are dissolved in 150 parts of water with 20 parts of calcined soda, cooled with ice and then with the Diazo compound from 29.2 parts of 4-benzoylamino -2-amino -1-benzenesulfonic acid added.
The dye that forms is partially separated out. The precipitation is completed by adding table salt, then it is made as neutral as possible, filtered and dried.
Claims (1)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH128909T CH128909A (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 |
---|---|---|---|
CH128909T CH128909A (en) | 1926-12-04 | 1926-12-04 | Process for the production of a new dye. |
CH127259T | 1926-12-04 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH128909A true CH128909A (en) | 1928-11-16 |
Family
ID=25710809
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH128909T CH128909A (en) | 1926-12-04 | 1926-12-04 | Process for the production of a new dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH128909A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1996022333A1 (en) * | 1995-01-20 | 1996-07-25 | Zeneca Limited | Monoazo pigments |
-
1926
- 1926-12-04 CH CH128909T patent/CH128909A/en unknown
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1996022333A1 (en) * | 1995-01-20 | 1996-07-25 | Zeneca Limited | Monoazo pigments |
US5919915A (en) * | 1995-01-20 | 1999-07-06 | Zeneca Limited | Azo pyrazolone pigments |
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