CH204149A - Process for the preparation of a water-soluble disazo dye. - Google Patents
Process for the preparation of a water-soluble disazo dye.Info
- Publication number
- CH204149A CH204149A CH204149DA CH204149A CH 204149 A CH204149 A CH 204149A CH 204149D A CH204149D A CH 204149DA CH 204149 A CH204149 A CH 204149A
- Authority
- CH
- Switzerland
- Prior art keywords
- water
- disazo dye
- preparation
- soluble disazo
- dye
- Prior art date
Links
- 125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 title claims description 5
- 238000000034 method Methods 0.000 title claims description 4
- 238000002360 preparation method Methods 0.000 title description 2
- 239000000975 dye Substances 0.000 claims description 9
- 239000002253 acid Substances 0.000 claims description 2
- 239000010985 leather Substances 0.000 claims description 2
- 238000004519 manufacturing process Methods 0.000 claims description 2
- 239000000843 powder Substances 0.000 claims description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 2
- 150000007513 acids Chemical class 0.000 claims 1
- 239000007864 aqueous solution Substances 0.000 description 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 230000008878 coupling Effects 0.000 description 1
- 238000010168 coupling process Methods 0.000 description 1
- 238000005859 coupling reaction Methods 0.000 description 1
- 150000008049 diazo compounds Chemical class 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 1
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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Description
Zusatzpatent zum Hauptpatent lZr. <B>200675.</B> Verfahren zur Rerstellung eines wasserlöslichen Disazofarbstoffes. Gegenstand des vorliegenden Zusatzpaten tes ist ein Verfahren zur Herstellung eines wa-sserlöslichen Disazofarbstoffes, welches dadurch gekennzeichnet ist, dass man 1,3- Dioxybenzol, mit<B>1</B> Mol. diazotierter 4-Amino- 1-benzylsulio,
nsäure und.<B>1</B> Mol. diazotierter 2-Amino-l-benzylsulfo,nsäure vereinigt.
<I>Beispiel:</I> Die aus<B>18,7</B> Gewiehtsteilen 4-Amino-l- benzylsulfonsäure in der üblichen Weise her gestellte wässerige Lösung der Diazoverbin- dung fliesst bei<B>0 ' C</B> unter Rühren in eine wässerige Lösung von<B>11</B> Gewichtsteilen 1,3- Dioxybenzol in Gegenwart von Natrium- carbona,t. Nach beendeter Kupplung fliesst zu dem gebildeten Farbstoff allmählich eine <I>aus</I><B>18,
7</B> Gewichtsteilen 2-Amino-l-benzyl- sulfonsäure erhaltene Diazosuspension. In sodaall-,alise,liem Medium ist die Bildung des Disazofarbstoffes rasch beendet. Der Farb- stoff wird ausgesalzen, isoliert und ge trocknet.
Er bildet ein dunkelbraunes Pulver, das sieh in Wasser mit brauner Farbe löst und Leder in rötlie,1-i braunen Tönen gut einfärbt.
Additional patent to the main patent lZr. <B> 200675. </B> Process for the preparation of a water-soluble disazo dye. The subject of the present additional patent is a process for the production of a water-soluble disazo dye, which is characterized in that 1,3-dioxybenzene, with <B> 1 </B> mol. 4-Amino-1-benzylsulio diazotized,
Acid and 1 mol of diazotized 2-amino-1-benzylsulfonic acid combined.
<I> Example: </I> The aqueous solution of the diazo compound produced in the customary manner from <B> 18.7 </B> parts by weight of 4-amino-1-benzylsulfonic acid flows at <B> 0 'C < / B> while stirring in an aqueous solution of <B> 11 </B> parts by weight of 1,3-dioxybenzene in the presence of sodium carbona, t. After the coupling has ended, an <I>aus</I> <B> 18 gradually flows to the dye formed,
7 parts by weight of 2-amino-1-benzylsulfonic acid diazo suspension obtained. In sodaall, alise, liem medium the formation of the disazo dye is quickly completed. The dye is salted out, isolated and dried.
It forms a dark brown powder which dissolves in water with a brown color and dyes leather well in reddish, 1-brown tones.
Claims (1)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE204149X | 1936-09-04 | ||
| CH200675T | 1938-10-31 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH204149A true CH204149A (en) | 1939-04-15 |
Family
ID=25723570
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH204149D CH204149A (en) | 1936-09-04 | 1937-08-19 | Process for the preparation of a water-soluble disazo dye. |
Country Status (1)
| Country | Link |
|---|---|
| CH (1) | CH204149A (en) |
-
1937
- 1937-08-19 CH CH204149D patent/CH204149A/en unknown
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