CH135397A - Process for the preparation of a new copper amine complex azo compound. - Google Patents
Process for the preparation of a new copper amine complex azo compound.Info
- Publication number
- CH135397A CH135397A CH135397DA CH135397A CH 135397 A CH135397 A CH 135397A CH 135397D A CH135397D A CH 135397DA CH 135397 A CH135397 A CH 135397A
- Authority
- CH
- Switzerland
- Prior art keywords
- azo compound
- amine complex
- complex azo
- copper amine
- 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
- C09B33/00—Disazo and polyazo dyes of the types A->K<-B, A->B->K<-C, or the like, prepared by diazotising and coupling
- C09B33/02—Disazo dyes
- C09B33/04—Disazo dyes in which the coupling component is a dihydroxy or polyhydroxy compound
- C09B33/056—Disazo dyes in which the coupling component is a dihydroxy or polyhydroxy compound the coupling component being a bis-(naphthol-urea)
-
- 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
- C09B45/00—Complex metal compounds of azo dyes
- C09B45/02—Preparation from dyes containing in o-position a hydroxy group and in o'-position hydroxy, alkoxy, carboxyl, amino or keto groups
- C09B45/24—Disazo or polyazo compounds
- C09B45/28—Disazo or polyazo compounds containing copper
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Description
<B>Zusatzpatent</B> zum Hauptpatent Nr. 133477. Verfahren zur Darstellung einer neuen Kupferamminkompleaazoverbindung. Es wurde gefunden, dass man zu einer neuen Kupferamminkomplexazoverbindung ge langen kann, indem man zunächst 1 Mol dianotierter 3-Aminobenzaldehyd essigsauer kuppelt mit 1 Mol 5.5'-Dioxy-2.2'-dinaphtyl- harnstoff-7.7'-disulfosäure;
zu dieser Azover- bindung setzt man Hexammincuprichlorid und weiter 1 Mol dianotierter 2-Aminobenzoesäure. Die erhaltene Kupferamminkomplexazoverbin- dung löst sich in Wasser mit ziegelroter Farbe und ist für die Färberei, Druckerei und als Schädlingsbekämpfungsmittel ver wendbar.
<I>Beispiel:</I> 121 Gewichtsteile 3-Amicrobenzaldehyd werden dianotiert und essigsauer mit 502 Gewichtsteilen 5.5'-Dioxy-2.-2'-dinaphtylharn- stoff-7.7'-disulfosäure gekuppelt. Nach been digter Umsetzung macht man mit 800 Ge wichtsteilen kalzinierter Soda alkalisch, setzt eine Lösung des Hexammincuprichlorids,
be reitet aus 170 Gewichtsteilen Cuprichlorid hinzu und kuppelt bei -f- 5 mit einer in bekannter Weise hergestellten Lösung der Diazoverbindung aus 137 Gewichtsteilen 2- Aminobenzoesäure. Man salzt die klare Farb- stofflösung, welche keine Spur von unlöslichen anorganischen Kupferverbindungen enthält, aus, filtriert und arbeitet in der üblichen Weise auf.
Die neue Kupferamrninkomplexazoverbin- dung löst sich in Wasser mit ziegelroter, in konzentrierter Schwefelsäure mit blaustichig roter Farbe.
<B> Additional patent </B> to the main patent No. 133477. Process for the preparation of a new copper amine incompleaazo compound. It has been found that a new copper amine complex azo compound can be obtained by first coupling 1 mol of dianotated 3-aminobenzaldehyde in acetic acidic acid with 1 mol of 5.5'-dioxy-2.2'-dinaphthyl urea-7.7'-disulfonic acid;
hexammine cuprichloride and a further 1 mol of dianotated 2-aminobenzoic acid are added to this azo compound. The copper amine complex azo compound obtained dissolves in water with a brick-red color and can be used in dyeing, printing and as a pesticide.
<I> Example: </I> 121 parts by weight of 3-amicrobenzaldehyde are dianotized and coupled to acetic acid with 502 parts by weight of 5.5'-dioxy-2.-2'-dinaphthylurea-7.7'-disulfonic acid. After finished conversion is made alkaline with 800 parts by weight of calcined soda, a solution of hexammine cuprichloride is used,
be prepared from 170 parts by weight of cupric chloride and coupled at -f- 5 with a solution of the diazo compound prepared in a known manner from 137 parts by weight of 2-aminobenzoic acid. The clear dye solution, which does not contain any trace of insoluble inorganic copper compounds, is salted out, filtered and worked up in the usual way.
The new copper amine complex azo compound dissolves in water with a brick-red color, and in concentrated sulfuric acid with a bluish red color.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH133477T | 1927-10-22 | ||
CH135397T | 1927-10-22 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH135397A true CH135397A (en) | 1929-09-15 |
Family
ID=25712094
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH135397D CH135397A (en) | 1927-10-22 | 1927-10-22 | Process for the preparation of a new copper amine complex azo compound. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH135397A (en) |
-
1927
- 1927-10-22 CH CH135397D patent/CH135397A/en unknown
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