CH128905A - Process for the production of a new dye. - Google Patents
Process for the production of a new dye.Info
- Publication number
- CH128905A CH128905A CH128905TA CH128905A CH 128905 A CH128905 A CH 128905A CH 128905T A CH128905T A CH 128905TA CH 128905 A CH128905 A CH 128905A
- Authority
- CH
- Switzerland
- Prior art keywords
- dye
- production
- new dye
- sulfonic acid
- acetamino
- 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
Verfahren zur Herstellung eines neuen Farbstoffes. Es wurde gefunden, dass man einen neuen Farbstoff erhält, wenn man diazotierte Farbstoff erhält, wenn man diazotierte 4- Acetamino-2-amino-l-benzolsulfosäure mit 1 pyrazolon kuppelt. Der so erhaltene Farb stoff bildet ein gelbes Pulver. Er färbt Wolle aus schwefelsaurem Bade in sehr. gleich mässigen, grüngelben Tönen. Die Färbungen sind sehr gut licht-, Wasser- und alkaliecht und halten der sauren Walke stand.
<I>Beispiel:</I> 39 Teile 1-(-2'-Chlor-4'-sulfosäure)-phe- nyl-3-methyl-5-pyrazolon werden in 150 Tei len Wasser mit 20 Teilen calcinierter Soda gelöst, mit Eis gekühlt und hierauf mit der Diazoverbindung aus 23 Teilen 4-Acetamino- 2-amino-l-benzolsulfosäure 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.
Process for the production of a new dye. It has been found that a new dye is obtained when diazotized dye is obtained when diazotized 4-acetamino-2-amino-1-benzenesulfonic acid is coupled with 1 pyrazolone. The dye obtained in this way forms a yellow powder. He dyes wool from a sulfuric acid bath in a very great deal. even, green-yellow tones. The dyeings are very resistant to light, water and alkali and withstand acidic fulling.
<I> Example: </I> 39 parts of 1- (- 2'-chloro-4'-sulfonic acid) -phenyl-3-methyl-5-pyrazolone are dissolved in 150 parts of water with 20 parts of calcined soda, cooled with ice and then mixed with the diazo compound from 23 parts of 4-acetamino-2-amino-1-benzenesulfonic 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 |
---|---|---|---|
CH128905T CH128905A (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 |
---|---|---|---|
CH128905T CH128905A (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 |
---|---|
CH128905A true CH128905A (en) | 1928-11-16 |
Family
ID=25710805
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH128905T CH128905A (en) | 1926-12-04 | 1926-12-04 | Process for the production of a new dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH128905A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7857948B2 (en) | 2006-07-19 | 2010-12-28 | Oerlikon Trading Ag, Trubbach | Method for manufacturing poorly conductive layers |
EP2355126A2 (en) | 2005-03-24 | 2011-08-10 | Oerlikon Trading AG, Trübbach | Hard material layer |
-
1926
- 1926-12-04 CH CH128905T patent/CH128905A/en unknown
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP2355126A2 (en) | 2005-03-24 | 2011-08-10 | Oerlikon Trading AG, Trübbach | Hard material layer |
US7857948B2 (en) | 2006-07-19 | 2010-12-28 | Oerlikon Trading Ag, Trubbach | Method for manufacturing poorly conductive layers |
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