CH128911A - Process for the production of a new dye. - Google Patents
Process for the production of a new dye.Info
- Publication number
- CH128911A CH128911A CH128911TA CH128911A CH 128911 A CH128911 A CH 128911A CH 128911T A CH128911T A CH 128911TA CH 128911 A CH128911 A CH 128911A
- Authority
- CH
- Switzerland
- Prior art keywords
- dye
- new dye
- production
- wool
- pyrazolone
- 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)
- Coloring (AREA)
Description
Zusatzpatent zum Hauptpatent Nr. <B>127259.</B> Verfahren zur Herstellung eines neuen Farbstoffes. Es wurde gefunden, dass man einen neuen Farbstoff erhält, wenn man diazotierte 4- Benzoylamino-2-amino-l-benzolsulfosäure mit 1-(3'-Chlor)-phenyl-3-methyl-5-pyrazolon kup pelt. Der so erhaltene Farbstoff bildet ein gelbes Pulver. Er färbt Wolle aus schwefel saurem Bade in sehr gleichmässigen, gelben Tönen. Die Färbungen sind sehr gut licht-, wasser-, wasch- und alkaliecht und halten der sauren Walke stand. Er ist auch zum Färben der gewöhnlichen und der chargierten Seide geeignet.
<I>Beispiel:</I> <B>20,9</B> Teile 1-(3'-Chlor)-pheiiyl-3-methyl-6- pyrazolon werden in<B>150</B> Teilen Wasser mit 20 Teilen calcinierter Soda und der nötigen Menge Natronlauge gelöst, mit Eis gekühlt und hierauf mit der Diazoverbindung aus<B>29,2</B> Teilen 4-Benzylamino-2-amino-l-benzolsulfo- säure versetzt. Der sich bildende Farbstoff scheidet sich teilweise aus. Durch Zusatz von Kochsalz wird die Fällung vervollständigt, dann wird möglichst neutral gestellt, filtriert und getrocknet.
Additional patent to main patent no. <B> 127259. </B> 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- (3'-chloro) -phenyl-3-methyl-5-pyrazolone. The dye thus obtained forms a yellow powder. He dyes wool from a sulphurous acid bath in very even, yellow tones. The dyeings are very light, water, wash and alkali-fast and withstand acidic milled wool. It is also suitable for dyeing ordinary and charged silk.
<I> Example: </I> <B> 20.9 </B> parts of 1- (3'-chloro) -pheiiyl-3-methyl-6-pyrazolone are used in <B> 150 </B> parts of water dissolved with 20 parts of calcined soda and the necessary amount of sodium hydroxide solution, cooled with ice and then mixed with the diazo compound of 29.2 parts of 4-benzylamino-2-amino-1-benzenesulphonic acid. The dye that forms 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 |
---|---|---|---|
CH128911T CH128911A (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 | ||
CH128911T CH128911A (en) | 1926-12-04 | 1926-12-04 | Process for the production of a new dye. |
Publications (1)
Publication Number | Publication Date |
---|---|
CH128911A true CH128911A (en) | 1928-11-16 |
Family
ID=25710811
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH128911T CH128911A (en) | 1926-12-04 | 1926-12-04 | Process for the production of a new dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH128911A (en) |
-
1926
- 1926-12-04 CH CH128911T patent/CH128911A/en unknown
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