CH129792A - Process for the production of a new azo dye. - Google Patents
Process for the production of a new azo dye.Info
- Publication number
- CH129792A CH129792A CH129792DA CH129792A CH 129792 A CH129792 A CH 129792A CH 129792D A CH129792D A CH 129792DA CH 129792 A CH129792 A CH 129792A
- Authority
- CH
- Switzerland
- Prior art keywords
- azo dye
- production
- mole
- new azo
- new
- Prior art date
Links
- 239000000987 azo dye Substances 0.000 title claims description 4
- 238000000034 method Methods 0.000 title claims description 3
- 238000004519 manufacturing process Methods 0.000 title description 2
- 239000000975 dye Substances 0.000 claims description 5
- 239000007859 condensation product Substances 0.000 claims description 3
- NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical compound CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 claims description 2
- 239000000843 powder Substances 0.000 claims description 2
- 210000002268 wool Anatomy 0.000 claims description 2
- 238000002360 preparation method Methods 0.000 claims 1
- VOZKAJLKRJDJLL-UHFFFAOYSA-N 2,4-diaminotoluene Chemical compound CC1=CC=C(N)C=C1N VOZKAJLKRJDJLL-UHFFFAOYSA-N 0.000 description 1
- 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
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 1
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 235000002639 sodium chloride Nutrition 0.000 description 1
- 239000011780 sodium chloride Substances 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
- C09B62/00—Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves
- C09B62/02—Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves with the reactive group directly attached to a heterocyclic ring
- C09B62/04—Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves with the reactive group directly attached to a heterocyclic ring to a triazine ring
- C09B62/08—Azo dyes
- C09B62/085—Monoazo dyes
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Description
<B>Zusatzpatent</B> zum Hauptpatent Nr. 113867. Verfahren zur Herstellung eines neuen Azofarbstoffes. Es wurde gefunden, dass man einen Azofarb- stoff, der in seinem Molekül einen Cyanurkern enthält, erhalten kann, wenn man 1 Mol. des diazotierten Kondensationsproduktes aus 11M1. m-Toliiylendiamici und 1 Mol. Cyanurtricar- bonsäurechlorid mit 1 Mol. 2,
5-Aininonaphthol- 7-sulfosäure kuppelt. Der neue Farbstoff bil det ein oranges Pulver und färbt Wolle in orangen Tönen an.
<I>Beispiel</I> 31,7 Teile des Kondensationsproduktes aus m-Toluylendiamin und Cyanurtricarbonsäure- chlorid werden wie üblich diazotiert und zu einer Lösung von 26,1 Teilen 2,5-Amino- iiaplithol-7-sulfosaures Natrium und 25 Teilen Soda gegeben. Der gebildete Farbstoff wird wie üblich mit Kochsalz gefällt, filtriert und getrocknet.
<B> Additional patent </B> to main patent no. 113867. Process for the production of a new azo dye. It has been found that an azo dye which contains a cyanuric nucleus in its molecule can be obtained if 1 mol. Of the diazotized condensation product from 11M1. m-Toliiylendiamici and 1 mol. Cyanurtricar- bonsäurechlorid with 1 mol. 2,
5-Ainonaphthol-7-sulfonic acid couples. The new dye forms an orange powder and dyes wool in orange tones.
<I> Example </I> 31.7 parts of the condensation product of m-tolylenediamine and cyanurotricarboxylic acid chloride are diazotized as usual and form a solution of 26.1 parts of 2,5-aminoaplithol-7-sulphonic acid sodium and 25 parts Given soda. The dye formed is precipitated as usual with common salt, filtered and dried.
Claims (1)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH129792T | 1924-10-07 | ||
| CH113867T | 1924-10-07 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH129792A true CH129792A (en) | 1929-01-02 |
Family
ID=25708230
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH129792D CH129792A (en) | 1924-10-07 | 1924-10-07 | Process for the production of a new azo dye. |
Country Status (1)
| Country | Link |
|---|---|
| CH (1) | CH129792A (en) |
-
1924
- 1924-10-07 CH CH129792D patent/CH129792A/en unknown
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