DE214496C - - Google Patents
Info
- Publication number
- DE214496C DE214496C DENDAT214496D DE214496DA DE214496C DE 214496 C DE214496 C DE 214496C DE NDAT214496 D DENDAT214496 D DE NDAT214496D DE 214496D A DE214496D A DE 214496DA DE 214496 C DE214496 C DE 214496C
- Authority
- DE
- Germany
- Prior art keywords
- aminophenyl
- amino
- ether
- black
- naphtol
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Active
Links
- 239000002253 acid Substances 0.000 claims description 31
- 239000000975 dye Substances 0.000 claims description 21
- GOJFAKBEASOYNM-UHFFFAOYSA-N 2-(2-aminophenoxy)aniline Chemical class NC1=CC=CC=C1OC1=CC=CC=C1N GOJFAKBEASOYNM-UHFFFAOYSA-N 0.000 claims description 16
- 150000008049 diazo compounds Chemical class 0.000 claims description 14
- -1 o-aminophenyl ether o-toluidine Chemical compound 0.000 claims description 14
- 210000002268 Wool Anatomy 0.000 claims description 13
- JMGOORYWTOXUQE-XOBOFAKPSA-N (6Z)-4-amino-3-[(4-nitrophenyl)diazenyl]-5-oxo-6-(phenylhydrazinylidene)naphthalene-2,7-disulfonic acid Chemical compound OS(=O)(=O)C1=CC=2C=C(S(O)(=O)=O)\C(=N/NC=3C=CC=CC=3)C(=O)C=2C(N)=C1N=NC1=CC=C([N+]([O-])=O)C=C1 JMGOORYWTOXUQE-XOBOFAKPSA-N 0.000 claims description 12
- RUFPHBVGCFYCNW-UHFFFAOYSA-N 1-Naphthylamine Chemical compound C1=CC=C2C(N)=CC=CC2=C1 RUFPHBVGCFYCNW-UHFFFAOYSA-N 0.000 claims description 10
- RTZKZFJDLAIYFH-UHFFFAOYSA-N diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 8
- HLBLWEWZXPIGSM-UHFFFAOYSA-N 4,4'-Oxydianiline Chemical compound C1=CC(N)=CC=C1OC1=CC=C(N)C=C1 HLBLWEWZXPIGSM-UHFFFAOYSA-N 0.000 claims description 6
- XJCVRTZCHMZPBD-UHFFFAOYSA-N 3-Nitroaniline Chemical compound NC1=CC=CC([N+]([O-])=O)=C1 XJCVRTZCHMZPBD-UHFFFAOYSA-N 0.000 claims description 5
- 230000002378 acidificating Effects 0.000 claims description 5
- 238000000034 method Methods 0.000 claims description 4
- KUOMPUAJULJTTD-UHFFFAOYSA-N NC=1C(=C(C(=CC1)C)OC1=C(C=CC(=C1C1=CC=CC=C1)N)C)C1=CC=CC=C1 Chemical compound NC=1C(=C(C(=CC1)C)OC1=C(C=CC(=C1C1=CC=CC=C1)N)C)C1=CC=CC=C1 KUOMPUAJULJTTD-UHFFFAOYSA-N 0.000 claims 1
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 claims 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-N HCl Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 16
- QYFYIOWLBSPSDM-UHFFFAOYSA-N 6-aminonaphthalen-1-ol Chemical compound OC1=CC=CC2=CC(N)=CC=C21 QYFYIOWLBSPSDM-UHFFFAOYSA-N 0.000 description 7
- 239000000243 solution Substances 0.000 description 7
- BVKZGUZCCUSVTD-UHFFFAOYSA-N Carbonic acid Chemical compound OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 description 5
- LSNNMFCWUKXFEE-UHFFFAOYSA-N sulfonic acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- LPXPTNMVRIOKMN-UHFFFAOYSA-M Sodium nitrite Chemical compound [Na+].[O-]N=O LPXPTNMVRIOKMN-UHFFFAOYSA-M 0.000 description 4
- 229920000742 Cotton Polymers 0.000 description 3
- 238000004040 coloring Methods 0.000 description 3
- 230000001808 coupling Effects 0.000 description 3
- 238000010168 coupling process Methods 0.000 description 3
- 238000005859 coupling reaction Methods 0.000 description 3
- 125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 description 3
- QPKNFEVLZVJGBM-UHFFFAOYSA-N 2-aminonaphthalen-1-ol Chemical compound C1=CC=CC2=C(O)C(N)=CC=C21 QPKNFEVLZVJGBM-UHFFFAOYSA-N 0.000 description 2
- QSNSCYSYFYORTR-UHFFFAOYSA-N 4-Chloroaniline Chemical compound NC1=CC=C(Cl)C=C1 QSNSCYSYFYORTR-UHFFFAOYSA-N 0.000 description 2
- ABJQKDJOYSQVFX-UHFFFAOYSA-N 4-aminonaphthalen-1-ol Chemical compound C1=CC=C2C(N)=CC=C(O)C2=C1 ABJQKDJOYSQVFX-UHFFFAOYSA-N 0.000 description 2
- UIIMBOGNXHQVGW-UHFFFAOYSA-M NaHCO3 Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
- HVBSAKJJOYLTQU-UHFFFAOYSA-N Sulfanilic acid Chemical compound NC1=CC=C(S(O)(=O)=O)C=C1 HVBSAKJJOYLTQU-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 239000000543 intermediate Substances 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 235000010288 sodium nitrite Nutrition 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- YHYKLKNNBYLTQY-UHFFFAOYSA-N 1,1-diphenylhydrazine Chemical compound C=1C=CC=CC=1N(N)C1=CC=CC=C1 YHYKLKNNBYLTQY-UHFFFAOYSA-N 0.000 description 1
- CYXMOAZSOPXQOD-UHFFFAOYSA-N 1-methyl-2-(2-methylphenoxy)benzene Chemical compound CC1=CC=CC=C1OC1=CC=CC=C1C CYXMOAZSOPXQOD-UHFFFAOYSA-N 0.000 description 1
- ZCGVPUAAMCMLTM-UHFFFAOYSA-N 2-amino-5-chlorobenzenesulfonic acid Chemical compound NC1=CC=C(Cl)C=C1S(O)(=O)=O ZCGVPUAAMCMLTM-UHFFFAOYSA-N 0.000 description 1
- AKCRQHGQIJBRMN-UHFFFAOYSA-N 2-chloroaniline Chemical compound NC1=CC=CC=C1Cl AKCRQHGQIJBRMN-UHFFFAOYSA-N 0.000 description 1
- HYLOSPCJTPLXSF-UHFFFAOYSA-N 5-amino-2-anilinobenzenesulfonic acid Chemical compound OS(=O)(=O)C1=CC(N)=CC=C1NC1=CC=CC=C1 HYLOSPCJTPLXSF-UHFFFAOYSA-N 0.000 description 1
- DADSZOFTIIETSV-UHFFFAOYSA-N N,N-dichloroaniline Chemical compound ClN(Cl)C1=CC=CC=C1 DADSZOFTIIETSV-UHFFFAOYSA-N 0.000 description 1
- JMLOUOMYQULDGG-UHFFFAOYSA-N NC1=C(C(=C(C=C1)C)C1=CC=CC=C1)OC=1C(=C(C=CC1N)C)C1=CC=CC=C1 Chemical compound NC1=C(C(=C(C=C1)C)C1=CC=CC=C1)OC=1C(=C(C=CC1N)C)C1=CC=CC=C1 JMLOUOMYQULDGG-UHFFFAOYSA-N 0.000 description 1
- SBOJXQVPLKSXOG-UHFFFAOYSA-N O-amino-Hydroxylamine Chemical compound NON SBOJXQVPLKSXOG-UHFFFAOYSA-N 0.000 description 1
- 241000872198 Serjania polyphylla Species 0.000 description 1
- BDKZHNJTLHOSDW-UHFFFAOYSA-N [Na].CC(O)=O Chemical compound [Na].CC(O)=O BDKZHNJTLHOSDW-UHFFFAOYSA-N 0.000 description 1
- 239000003929 acidic solution Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 238000004043 dyeing Methods 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 239000001046 green dye Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 238000005185 salting out Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 239000000126 substance 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
- 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
- C09B33/08—Disazo dyes in which the coupling component is a hydroxy-amino compound
- C09B33/10—Disazo dyes in which the coupling component is a hydroxy-amino compound in which the coupling component is an amino naphthol
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE214496C true DE214496C (it) |
Family
ID=476071
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DENDAT214496D Active DE214496C (it) |
Country Status (1)
| Country | Link |
|---|---|
| DE (1) | DE214496C (it) |
-
0
- DE DENDAT214496D patent/DE214496C/de active Active
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE214496C (it) | ||
| DE2230300C2 (de) | Disazofarbstoffe und ihre Herstellung | |
| AT43178B (de) | Verfahren zur Darstellung von sauren Wollfarbstoffen. | |
| DE842975C (de) | Verfahren zur Herstellung von Monoazofarbstoffen | |
| DE82074C (it) | ||
| DE2139148C3 (de) | Telrakisazofarbstoffe, Verfahren zu deren Herstellung und ihre Verwendung zum Färben vonpflanzlichen und tierischen Fasermaterialien, sowie von Leder | |
| DE636358C (de) | Verfahren zur Herstellung von kupferhaltigen Azofarbstoffen | |
| DE87671C (it) | ||
| DE469288C (de) | Verfahren zur Darstellung entwickelbarer Trisazofarbstoffe | |
| DE393267C (de) | Verfahren zur Darstellung von wasserunloeslichen Azofarbstoffen | |
| DE617999C (de) | Verfahren zur Herstellung von chromhaltigen Azofarbstoffen | |
| DE1644391B1 (de) | Trisazofarbstoffe | |
| DE286091C (it) | ||
| DE118655C (it) | ||
| DE2453209A1 (de) | Disazofarbstoffe | |
| DE243122C (it) | ||
| DE587449C (de) | Verfahren zur Herstellung von primaeren Disazofarbstoffen | |
| DE1644168C3 (it) | ||
| DE217627C (it) | ||
| DE732437C (de) | Verfahren zur Herstellung von wasserunloeslichen Azofarbstoffen | |
| DE138902C (it) | ||
| DE163040C (it) | ||
| DE288839C (it) | ||
| DE66886C (de) | Verfahren zur Darstellung indulinartiger Farbstoffe aus Azoverbindungen des Benzidins und Diamidotriphenylmethans | |
| DE748823C (de) | Verfahren zur Herstellung von Dis- und Tetrakisazofarbstoffen |