CH90846A - Process for the preparation of a diazotization dye. - Google Patents
Process for the preparation of a diazotization dye.Info
- Publication number
- CH90846A CH90846A CH90846DA CH90846A CH 90846 A CH90846 A CH 90846A CH 90846D A CH90846D A CH 90846DA CH 90846 A CH90846 A CH 90846A
- Authority
- CH
- Switzerland
- Prior art keywords
- dye
- diazotization
- preparation
- oxy
- mole
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims description 3
- 238000006193 diazotization reaction Methods 0.000 title claims 2
- 239000000975 dye Substances 0.000 claims description 9
- DETXZQGDWUJKMO-UHFFFAOYSA-N 2-hydroxymethanesulfonic acid Chemical compound OCS(O)(=O)=O DETXZQGDWUJKMO-UHFFFAOYSA-N 0.000 claims description 4
- 229920000742 Cotton Polymers 0.000 claims description 2
- 238000004519 manufacturing process Methods 0.000 claims description 2
- 238000004040 coloring Methods 0.000 claims 1
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- 239000000203 mixture Substances 0.000 description 2
- DWAQJAXMDSEUJJ-UHFFFAOYSA-M Sodium bisulfite Chemical compound [Na+].OS([O-])=O DWAQJAXMDSEUJJ-UHFFFAOYSA-M 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 235000010267 sodium hydrogen sulphite Nutrition 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-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
- C09B35/00—Disazo and polyazo dyes of the type A<-D->B prepared by diazotising and coupling
- C09B35/02—Disazo dyes
- C09B35/039—Disazo dyes characterised by the tetrazo component
- C09B35/205—Disazo dyes characterised by the tetrazo component the tetrazo component being a derivative of a diaryl- or triaryl- alkane or-alkene
- C09B35/21—Disazo dyes characterised by the tetrazo component the tetrazo component being a derivative of a diaryl- or triaryl- alkane or-alkene of diarylmethane or triarylmethane
-
- 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
- C09B35/00—Disazo and polyazo dyes of the type A<-D->B prepared by diazotising and coupling
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06P—DYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
- D06P3/00—Special processes of dyeing or printing textiles, or dyeing leather, furs, or solid macromolecular substances in any form, classified according to the material treated
- D06P3/58—Material containing hydroxyl groups
- D06P3/60—Natural or regenerated cellulose
- D06P3/68—Preparing azo dyes on the material
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Coloring (AREA)
Description
Verfahren zur Herstellung eines Diäzotierängsfarbstoffes. Es wurde gefunden, dass durch Einwirkung von Formaldehydbisulfit auf den Farbstoff, erhalten durch Kombinieren von 1 Mol. tetrazo- tiertem 3 : 3'-Diainino-4 .# 4'-ditolylmethan mit Mol: 1 : 2-(3'-Aminophenyl)-riapbtimidazol-* 5-oxy-7-srilfosäure, ein leichtlöslicher Farbstoff erhalten wird.
Dieser Farbstoff färbt uuge- beizte Baumwolle gelbstichig Bordeaux; durch r .Diazotieren der Färbung und Kuppeln mit ss-Naphtal wird ein sehr waschechtes, volles Blaurot erhalten.
<I>Beispiel:</I> 50 Teile des Farbstoffes aus 1 Mol. tetra- zotiertem 3:3'-Diainino-4:4'-ditolylmetliän und 2 Mol. 1 :
2-(3'-Amiriopheriyl)-riaphtirnid-. azol-5-oxy-7-srilfosäure werden mit 300 Teilen Wasser angerührt und finit einer vorbei zum Kochen erhitzten Mischung von 28,6 'feilen Natriumbisulfitlösung h, 400o und 3,3 Teilen Formaldehyd in Form einer wässerigen 30 bis 40 /oigen Lösung versetzt.- Man erhitzt die 112asse-während -einer Stunde zum Sieden, salzt aus, filtriert ünd trocknet.
Process for the production of a longitudinal dyestuff. It has been found that by the action of formaldehyde bisulfite on the dye, obtained by combining 1 mole of tetrazolated 3: 3'-diainino-4. # 4'-ditolylmethane with mole: 1: 2- (3'-aminophenyl) -riapbtimidazole- * 5-oxy-7-srilfosäure, a readily soluble dye is obtained.
This dye gives off-stained cotton a yellowish tinge of Bordeaux; by r. diazotizing the color and domes with SS-naphthalene a very washfast, full blue-red is obtained.
<I> Example: </I> 50 parts of the dye from 1 mol. Tetrazotized 3: 3'-diainino-4: 4'-ditolylmetliän and 2 mol. 1:
2- (3'-Amiriopheriyl) -riaphtirnid-. azole-5-oxy-7-sulfonic acid are mixed with 300 parts of water and finitely added to a mixture, heated to boiling point, of 28.6 'file sodium bisulfite solution, 400o and 3.3 parts of formaldehyde in the form of an aqueous 30 to 40% solution - The mixture is heated to the boil for one hour, salted out, filtered and dried.
Claims (1)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH90846T | 1918-12-21 | ||
| CH89557T | 1918-12-21 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH90846A true CH90846A (en) | 1921-09-16 |
Family
ID=25704030
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH90846D CH90846A (en) | 1918-12-21 | 1918-12-21 | Process for the preparation of a diazotization dye. |
Country Status (1)
| Country | Link |
|---|---|
| CH (1) | CH90846A (en) |
-
1918
- 1918-12-21 CH CH90846D patent/CH90846A/en unknown
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