CH191012A - Process for the production of a new azo dye. - Google Patents
Process for the production of a new azo dye.Info
- Publication number
- CH191012A CH191012A CH191012DA CH191012A CH 191012 A CH191012 A CH 191012A CH 191012D A CH191012D A CH 191012DA CH 191012 A CH191012 A CH 191012A
- Authority
- CH
- Switzerland
- Prior art keywords
- production
- azo dye
- new azo
- new
- dye
- Prior art date
Links
- 239000000987 azo dye Substances 0.000 title claims description 4
- 239000000975 dye Substances 0.000 claims description 5
- DSNYFFJTZPIKFZ-UHFFFAOYSA-N propoxybenzene Chemical compound CCCOC1=CC=CC=C1 DSNYFFJTZPIKFZ-UHFFFAOYSA-N 0.000 claims description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 3
- 239000010985 leather Substances 0.000 claims description 2
- 239000000843 powder Substances 0.000 claims description 2
- JVMSQRAXNZPDHF-UHFFFAOYSA-N 2,4-diaminobenzenesulfonic acid Chemical compound NC1=CC=C(S(O)(=O)=O)C(N)=C1 JVMSQRAXNZPDHF-UHFFFAOYSA-N 0.000 claims 1
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- LPXPTNMVRIOKMN-UHFFFAOYSA-M sodium nitrite Chemical compound [Na+].[O-]N=O LPXPTNMVRIOKMN-UHFFFAOYSA-M 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 1
- 125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 235000010288 sodium nitrite Nutrition 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
- C09B29/00—Monoazo dyes prepared by diazotising and coupling
- C09B29/06—Monoazo dyes prepared by diazotising and coupling from coupling components containing amino as the only directing group
- C09B29/08—Amino benzenes
-
- 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
- C09B29/00—Monoazo dyes prepared by diazotising and coupling
- C09B29/06—Monoazo dyes prepared by diazotising and coupling from coupling components containing amino as the only directing group
- C09B29/08—Amino benzenes
- C09B29/0801—Amino benzenes containing acid groups, e.g. COOH, SO3H, PO3H2, OSO3H, OPO3H2; SO2NHSO2R or salts thereof, R being hydrocarbonyls
- C09B29/0803—Amino benzenes containing acid groups, e.g. COOH, SO3H, PO3H2, OSO3H, OPO3H2; SO2NHSO2R or salts thereof, R being hydrocarbonyls containing SO3H, OSO3H
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Description
Verfahren zur Herstellung eines neuen Azofarbstoffes. Es wurde gefunden, dass man einen neuen Azofarbstoff erhält, wenn man diazotiertes 1-Amino-4-(f, r-dioxy) propyloxybenzol mit 1,3-Diaminobecizol-4-sul Tonsäure vereinigt. Der neue Farbstoff bildet ein dunkelbraunes Pul ver, das sich in Wasser mit brauner Farbe löst. Es färbt Leder in grünstichig-braunen Tönen vollständig durch.
<I>Beispiel:</I> 18,3 Teile 1-Amino-4-(ss, r-dioxy) propyl- oxybenzol werden in verdünnter Salzsäure gelöst und unter Zusatz von 6,9 Teilen Na triumnitrit diazotiert. Die klare Diazolösung vereinigt man bei<B>5-101</B> mit einer Lösung von 18,8 Teilen 1,3-Diaminobeuzol-4-sulfon- säure in 300 Teilen Wasser und 30 Teilen Natriumcarbonat.
Nach Beendigung der Farbstoffbildung wird aufgewärmt und ausgesalzen.
Process for the production of a new azo dye. It has been found that a new azo dye is obtained when diazotized 1-amino-4- (f, r-dioxy) propyloxybenzene is combined with 1,3-diaminobecizol-4-sulphonic acid. The new dye forms a dark brown powder that dissolves in water with a brown color. It completely dyes leather in greenish brown tones.
<I> Example: </I> 18.3 parts of 1-amino-4- (ss, r-dioxy) propyl oxybenzene are dissolved in dilute hydrochloric acid and diazotized with the addition of 6.9 parts of sodium nitrite. The clear diazo solution is combined at 5-101 with a solution of 18.8 parts of 1,3-diaminobeuzene-4-sulfonic acid in 300 parts of water and 30 parts of sodium carbonate.
After the dye has formed, it is warmed up and salted out.
Claims (1)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH191012T | 1936-03-06 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH191012A true CH191012A (en) | 1937-05-31 |
Family
ID=4437373
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH191012D CH191012A (en) | 1936-03-06 | 1936-03-06 | Process for the production of a new azo dye. |
Country Status (1)
| Country | Link |
|---|---|
| CH (1) | CH191012A (en) |
-
1936
- 1936-03-06 CH CH191012D patent/CH191012A/en unknown
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