CH393597A - Verfahren zur Herstellung von blauen sauren Anthrachinonfarbstoffen - Google Patents
Verfahren zur Herstellung von blauen sauren AnthrachinonfarbstoffenInfo
- Publication number
- CH393597A CH393597A CH886760A CH886760A CH393597A CH 393597 A CH393597 A CH 393597A CH 886760 A CH886760 A CH 886760A CH 886760 A CH886760 A CH 886760A CH 393597 A CH393597 A CH 393597A
- Authority
- CH
- Switzerland
- Prior art keywords
- weight
- parts
- anthraquinone dyes
- preparation
- good
- Prior art date
Links
- 230000002378 acidificating effect Effects 0.000 title claims description 6
- 239000001000 anthraquinone dye Substances 0.000 title claims description 4
- 238000000034 method Methods 0.000 title claims description 3
- 238000002360 preparation method Methods 0.000 title description 2
- QZZSAWGVHXXMID-UHFFFAOYSA-N 1-amino-4-bromo-9,10-dioxoanthracene-2-sulfonic acid Chemical compound C1=CC=C2C(=O)C3=C(Br)C=C(S(O)(=O)=O)C(N)=C3C(=O)C2=C1 QZZSAWGVHXXMID-UHFFFAOYSA-N 0.000 claims description 4
- 150000001412 amines Chemical class 0.000 claims description 3
- 238000009833 condensation Methods 0.000 claims description 3
- 230000005494 condensation Effects 0.000 claims description 3
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims description 3
- -1 Sulfuric acid ester Chemical class 0.000 claims description 2
- 238000004519 manufacturing process Methods 0.000 claims 1
- 239000000975 dye Substances 0.000 description 14
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 7
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 6
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 4
- SCVFZCLFOSHCOH-UHFFFAOYSA-M potassium acetate Chemical compound [K+].CC([O-])=O SCVFZCLFOSHCOH-UHFFFAOYSA-M 0.000 description 4
- GRGSHONWRKRWGP-UHFFFAOYSA-N 2-amino-4-sulfobenzoic acid Chemical compound NC1=CC(S(O)(=O)=O)=CC=C1C(O)=O GRGSHONWRKRWGP-UHFFFAOYSA-N 0.000 description 3
- 229920003043 Cellulose fiber Polymers 0.000 description 3
- 150000003931 anilides Chemical class 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 description 2
- 238000004043 dyeing Methods 0.000 description 2
- 230000032050 esterification Effects 0.000 description 2
- 238000005886 esterification reaction Methods 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 235000011056 potassium acetate Nutrition 0.000 description 2
- 239000004627 regenerated cellulose Substances 0.000 description 2
- BOCCWHAEFWQQNX-UHFFFAOYSA-N 2-acetamido-4-chlorosulfonylbenzoic acid Chemical compound CC(=O)NC1=CC(S(Cl)(=O)=O)=CC=C1C(O)=O BOCCWHAEFWQQNX-UHFFFAOYSA-N 0.000 description 1
- PHMWWTWNTMTDPZ-UHFFFAOYSA-N 2-acetamido-4-sulfinobenzoic acid Chemical compound C(C)(=O)NC=1C=C(C=CC1C(=O)O)S(=O)O PHMWWTWNTMTDPZ-UHFFFAOYSA-N 0.000 description 1
- SZIFAVKTNFCBPC-UHFFFAOYSA-N 2-chloroethanol Chemical compound OCCCl SZIFAVKTNFCBPC-UHFFFAOYSA-N 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 238000003776 cleavage reaction Methods 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 239000007859 condensation product Substances 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000001103 potassium chloride Substances 0.000 description 1
- 235000011164 potassium chloride Nutrition 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 230000007017 scission Effects 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 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
- C09B1/00—Dyes with anthracene nucleus not condensed with any other ring
- C09B1/16—Amino-anthraquinones
- C09B1/20—Preparation from starting materials already containing the anthracene nucleus
- C09B1/26—Dyes with amino groups substituted by hydrocarbon radicals
- C09B1/32—Dyes with amino groups substituted by hydrocarbon radicals substituted by aryl groups
- C09B1/34—Dyes with amino groups substituted by hydrocarbon radicals substituted by aryl groups sulfonated
- C09B1/343—Dyes with amino groups substituted by hydrocarbon radicals substituted by aryl groups sulfonated only sulfonated in the anthracene nucleus
-
- 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
- C09B62/44—Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves with the reactive group not directly attached to a heterocyclic ring
- C09B62/503—Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves with the reactive group not directly attached to a heterocyclic ring the reactive group being an esterified or non-esterified hydroxyalkyl sulfonyl or mercaptoalkyl sulfonyl group, a quaternised or non-quaternised aminoalkyl sulfonyl group, a heterylmercapto alkyl sulfonyl group, a vinyl sulfonyl or a substituted vinyl sulfonyl group, or a thiophene-dioxide group
- C09B62/505—Anthracene dyes
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DEF29136A DE1154892B (de) | 1959-08-08 | 1959-08-08 | Verfahren zur Herstellung von blauen sauren Anthrachinonfarbstoffen |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH393597A true CH393597A (de) | 1965-06-15 |
Family
ID=7093175
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH886760A CH393597A (de) | 1959-08-08 | 1960-08-04 | Verfahren zur Herstellung von blauen sauren Anthrachinonfarbstoffen |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US3097216A (en, 2012) |
| BE (1) | BE593892A (en, 2012) |
| CH (1) | CH393597A (en, 2012) |
| DE (1) | DE1154892B (en, 2012) |
| GB (1) | GB956801A (en, 2012) |
| NL (2) | NL127871C (en, 2012) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1235466B (de) * | 1960-12-01 | 1967-03-02 | Hoechst Ag | Verfahren zur Herstellung von organischen Farbstoffen |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2670265A (en) * | 1954-02-23 | Process | ||
| US2195067A (en) * | 1937-07-26 | 1940-03-26 | Gen Aniline & Film Corp | Wool dyestuffs of the anthraquinone series |
| US2453104A (en) * | 1946-06-21 | 1948-11-02 | Gen Aniline & Film Corp | Aminoanthraquinone sulfonamides |
| DE965902C (de) * | 1949-07-19 | 1957-09-19 | Hoechst Ag | Verfahren zum Fixieren wasserloeslicher organischer Verbindungen auf Unterlagen faseriger Struktur |
| US2583520A (en) * | 1949-09-16 | 1952-01-22 | Ciba Ltd | Quinazoline derivative vat dyestuffs |
-
0
- NL NL254453D patent/NL254453A/xx unknown
- NL NL127871D patent/NL127871C/xx active
-
1959
- 1959-08-08 DE DEF29136A patent/DE1154892B/de active Pending
-
1960
- 1960-08-01 US US46369A patent/US3097216A/en not_active Expired - Lifetime
- 1960-08-04 CH CH886760A patent/CH393597A/de unknown
- 1960-08-08 BE BE593892A patent/BE593892A/fr unknown
- 1960-08-08 GB GB27484/60A patent/GB956801A/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| NL127871C (en, 2012) | |
| NL254453A (en, 2012) | |
| DE1154892B (de) | 1963-09-26 |
| BE593892A (fr) | 1961-02-08 |
| US3097216A (en) | 1963-07-09 |
| GB956801A (en) | 1964-04-29 |
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