CH217954A - Process for the preparation of a disazo dye. - Google Patents
Process for the preparation of a disazo dye.Info
- Publication number
- CH217954A CH217954A CH217954DA CH217954A CH 217954 A CH217954 A CH 217954A CH 217954D A CH217954D A CH 217954DA CH 217954 A CH217954 A CH 217954A
- Authority
- CH
- Switzerland
- Prior art keywords
- dye
- parts
- greenish
- disazo dye
- preparation
- 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
- C09B31/00—Disazo and polyazo dyes of the type A->B->C, A->B->C->D, or the like, prepared by diazotising and coupling
- C09B31/02—Disazo dyes
- C09B31/04—Disazo dyes from a coupling component "C" containing a directive amino group
- C09B31/053—Amino naphthalenes
- C09B31/057—Amino naphthalenes containing acid groups, e.g. —CO2H, —SO3H, —PO3H2, —OSO3H, —OPO2H2; Salts thereof
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Description
Zusatzpatent zum Hauptpatent Nr. 214613. Verfahren zur Herstellung eines Disazofarbstoffes. Gegenstand des vorliegenden Zusatzpaten tes ist ein Verfahren zur Herstellung eines Disazofarbstoffes, daduTCh gekennzeichnet, dass dianotierte 2-Ch'lar-5-aminodip'henylsul- fon-3'-s:
ulfonsäure mit 1-Aminonaplithalin vereinigt, der entstandene Monoazofarbstoff weiter dianotiert und die D.iazoazoverbin- dung mit 1-Phenylaminonaphthalin-8-sulfon- säure gekuppelt wird.. Der neue Farbstoff stellt ein dunkles Pulver dar.
Er löst sich in Wasser mit grünstichi@g, in Schwefelsäure mit blauer Farbe und färbt Wolle aus schwach saurem Bade, in grüns.tichigen Tönen von hervorragender Walk-, Seewasser- und Lichtechtheit.
<I>Beispiel:</I> 34,8 Teile 2-Ch'lor-5-aminodiphenylsul- fon-3'-sulfonsäure werden in 100 Teilen Wasser mit 5"4 Teilen Soda, neutral gelöst, mit 6,9 Teilen Natriumnitrit versetzt und bei 3-5 in 29,2 Teile Salzsäure 30 % ein fliessen gelassen. Nach beendeter Dianotie rung kuppelt man, wie üblich mit 14,
3- Teilen 1-Aminonaphthalin. Der fertige Manoazo- farbstoff wird mit Socfa eben lackmus@alka- liscU gestellt, mit 7,2 Teilen Natriumnitrit versetzt und durch Eingiessen von 85 Teilen Salzsäure<B>30%</B> bei<B>8-10'</B> dianotiert. Nach dem die Diazotlerung beendet ist, wird ab filtriert, in 400 Teilen Wasser aufge schlämmt und mit<B>29,
5</B> Teilen 1-phenyl- aminonapbtha'lin-8-sulfonsaurem Natrium in Gegenwart von 45 Teilen essigsaurem Na trium essigsawer gekuppelt. Der getrocknete Farbstoff stellt ein dunkles Pulver dar.
Er löst sich in Wasser mit ;grünstichig, in Schwefelsäure mit blauer Farbe und färbt Wolle aus schwach saurem Bade in grün- Gtchigen Tönen von hervorragender Walk-, Seewasser- und Lichtechtheit.
Additional patent to main patent No. 214613. Process for the production of a disazo dye. The subject of the present additional patent is a process for the production of a disazo dye, characterized by the fact that dianotated 2-Ch'lar-5-aminodip'henylsulphon-3'-s:
Sulphonic acid combined with 1-aminonaplithalin, the resulting monoazo dye is further dianotized and the D.iazoazo compound is coupled with 1-phenylaminonaphthalene-8-sulphonic acid. The new dye is a dark powder.
It dissolves in water with a greenish tinge, in sulfuric acid with a blue color and dyes wool from weakly acidic baths in greenish tinted shades of excellent fullness, seawater and lightfastness.
<I> Example: </I> 34.8 parts of 2-chloro-5-aminodiphenylsulphone-3'-sulphonic acid are dissolved in 100 parts of water with 5 "4 parts of soda, neutral, with 6.9 parts of sodium nitrite added and allowed to flow in at 3-5 in 29.2 parts of 30% hydrochloric acid. After the end of the dianotation, coupling is carried out as usual with 14,
3- parts of 1-aminonaphthalene. The finished manoazo dye is made with Socfa just litmus @ alkali, mixed with 7.2 parts of sodium nitrite and poured in 85 parts of hydrochloric acid <B> 30% </B> at <B> 8-10 '</ B > dianotiert. After the diazotization has ended, it is filtered off, slurried in 400 parts of water and treated with <B> 29,
5 parts of 1-phenyl aminonapbtha'lin-8-sulfonic acid sodium in the presence of 45 parts of acetic acid sodium acetic acid coupled. The dried dye is a dark powder.
It dissolves in water with a; greenish tinge, in sulfuric acid with a blue color and dyes wool from weakly acidic baths in green-yellow tones of excellent fullness, seawater and lightfastness.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH217954T | 1939-12-11 | ||
CH214613T | 1939-12-11 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH217954A true CH217954A (en) | 1941-11-15 |
Family
ID=25725619
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH217954D CH217954A (en) | 1939-12-11 | 1939-12-11 | Process for the preparation of a disazo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH217954A (en) |
-
1939
- 1939-12-11 CH CH217954D patent/CH217954A/en unknown
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