CH128907A - Process for the production of a new dye. - Google Patents
Process for the production of a new dye.Info
- Publication number
- CH128907A CH128907A CH128907TA CH128907A CH 128907 A CH128907 A CH 128907A CH 128907T A CH128907T A CH 128907TA CH 128907 A CH128907 A CH 128907A
- Authority
- CH
- Switzerland
- Prior art keywords
- production
- new dye
- dye
- acetamino
- sulfophenyl
- 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
Description
Zusatzpatent zum Hauptpatent Nr. 127259. Verfahren zur Herstellung eines neuen Farbstoffes. Es wurde gefunden, dass man einen neuen Farbstoff erhält, wenn man diazotierte 4- A.cetamino-2-a:mino-l-benzolsulfosäure mit 1- m-Sulfophenyl-3-methyl-5-pyrazolon kuppelt. Der so erhaltene Farbstoff bildet ein gelbes Pulver. Er färbt Wolle aus schwefelsaurem Bade in sehr gleichmässigen, rotgelben Tönen. Die Färbungen sind sehr gut licht-, wasser- und alkaliecht und halten der sauren Walke stand.
<I>Beispiel:</I> 25,5 Teile 1-m-Sulfophenyl-3-methvl-5- pyrazolon werden in 150 Teilen Wasser mit 20 Teilen calcinierter Soda gelöst, mit Eis gekühlt und hierauf mit der Diazoverbindung aus 23 Teilen 4-Acetamino-2-amino-l-benzol- sulfosäure versetzt. Der sich bildende Farb- stoff scheidet sich teilweise aus. Durch Zu satz von Kochsalz wird die Fällung vervoll ständigt, dann wird möglichst neutral ge stellt, filtriert und getrocknet.
Additional patent to main patent no. 127259. Process for the production of a new dye. It has been found that a new dye is obtained when diazotized 4-a-acetamino-2-a: mino-1-benzenesulfonic acid is coupled with 1-m-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 dyeings are very resistant to light, water and alkali and withstand acidic fulling.
<I> Example: </I> 25.5 parts of 1-m-sulfophenyl-3-methvl-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-benzene sulfonic acid added. The dye that forms is partially eliminated. 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 |
---|---|---|---|
CH128907T CH128907A (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 | ||
CH128907T CH128907A (en) | 1926-12-04 | 1926-12-04 | Process for the production of a new dye. |
Publications (1)
Publication Number | Publication Date |
---|---|
CH128907A true CH128907A (en) | 1928-11-16 |
Family
ID=25710807
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH128907T CH128907A (en) | 1926-12-04 | 1926-12-04 | Process for the production of a new dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH128907A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4594411A (en) * | 1981-08-24 | 1986-06-10 | Basf Aktiengesellschaft | Sulfonated monoazo colorant lake obtained by di-azo coupling of 5-acetylamino-2-aminobenzene-1-sulfonic acid with 1-(3'-sulfophenyl)-3-methylphyrazol-5-one |
WO1996022333A1 (en) * | 1995-01-20 | 1996-07-25 | Zeneca Limited | Monoazo pigments |
-
1926
- 1926-12-04 CH CH128907T patent/CH128907A/en unknown
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4594411A (en) * | 1981-08-24 | 1986-06-10 | Basf Aktiengesellschaft | Sulfonated monoazo colorant lake obtained by di-azo coupling of 5-acetylamino-2-aminobenzene-1-sulfonic acid with 1-(3'-sulfophenyl)-3-methylphyrazol-5-one |
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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