CH135398A - 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
- CH135398A CH135398A CH135398DA CH135398A CH 135398 A CH135398 A CH 135398A CH 135398D A CH135398D A CH 135398DA CH 135398 A CH135398 A CH 135398A
- Authority
- CH
- Switzerland
- Prior art keywords
- azo compound
- amine complex
- preparation
- complex azo
- new copper
- 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)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Zusatzpatent zum Hauptpatent Nr. 133477. Verfahren zur Darstellung einer neuen Kupferamminkomplegazoverbindung. Es wurde gefunden, dass man zu einer neuen Kupferamminkomplexazoverbindung ge langen kann, indem man zunächst 1 Mol dianotierte 3-Amino-benzoesäure mit 1 Mol 7.7'-Disulfo- 5.5'-dioxy-2.2-dinaphtylharnstoff essigsauer kuppelt;
zu dieser Azoverbindung setzt man Hexammincuprichlorid und ein Mol dianotierte 2-Aminobenzoesäure, worauf sich eine Kupferamminkomplexazoverbindung bil det. Beispiel: 137 Gewichtsteile 3-Amir)obenzoesäure 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 Gew:chtsteilen Cuprichlorid, hinzu und kuppelt bei -%5 mit einer in be kannter Weise hergestellten Lösung der Diazo- verbindung aus 137 Gewichtsteilen 2-Amino- benzoesäure. Man salzt die klare Farbstoff lösung, welche keine Spur von unlöslicher), anorganischen Kupferverbindungen enthält, aus, filtriert und arbeitet in der üblichen Weise auf.
Die neue Kupferarnminkomplexazover- bindung löst sich in Wasser mit ziegelroter, in konzentrierter Schwefelsäure mit blaustichig roter Farbe, sie ist in der Druckerei, Färberei und als Schädlingsbekämpfungsmittel ver wendbar.
Additional patent to the main patent No. 133477. Process for the preparation of a new copper amine complex. It has been found that a new copper amine complex azo compound can be obtained by first coupling 1 mol of dianotated 3-amino-benzoic acid with 1 mol of 7.7'-disulfo-5.5'-dioxy-2.2-dinaphthylurea in acetic acidic acid;
Hexammine cuprichloride and one mole of dianotated 2-aminobenzoic acid are added to this azo compound, whereupon a copper amine complex azo compound is formed. Example: 137 parts by weight of 3-amir) topzoic acid are dianotized and acetic acid coupled with 502 parts by weight of 5.5'-dioxy-2.2'-dinaphthylurea-7.7-disulfonic acid.
When the reaction is complete, it is made alkaline with 800 parts by weight of calcined soda, a solution of hexammine cuprichloride, prepared from 170 parts by weight of cuprichloride, is added and, at -% 5, it is coupled with a solution of the diazo compound from 137 prepared in a known manner Parts by weight of 2-amino benzoic 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, in concentrated sulfuric acid with a bluish red color; it can be used in printing, dyeing and as a pesticide.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH135398T | 1927-10-22 | ||
CH133477T | 1927-10-22 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH135398A true CH135398A (en) | 1929-09-15 |
Family
ID=25712095
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH135398D CH135398A (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) | CH135398A (en) |
-
1927
- 1927-10-22 CH CH135398D patent/CH135398A/en unknown
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