DE206954C - - Google Patents
Info
- Publication number
- DE206954C DE206954C DE1906206954D DE206954DA DE206954C DE 206954 C DE206954 C DE 206954C DE 1906206954 D DE1906206954 D DE 1906206954D DE 206954D A DE206954D A DE 206954DA DE 206954 C DE206954 C DE 206954C
- Authority
- DE
- Germany
- Prior art keywords
- mol
- sulfonic acid
- black
- component
- blue
- 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.)
- Expired - Lifetime
Links
- 239000000975 dye Substances 0.000 claims description 19
- 150000001875 compounds Chemical class 0.000 claims description 5
- -1 polyazo Polymers 0.000 claims description 4
- 125000003630 glycyl group Chemical group [H]N([H])C([H])([H])C(*)=O 0.000 claims description 3
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 2
- 238000000034 method Methods 0.000 claims description 2
- ZBIBQNVRTVLOHQ-UHFFFAOYSA-N 5-aminonaphthalen-1-ol Chemical compound C1=CC=C2C(N)=CC=CC2=C1O ZBIBQNVRTVLOHQ-UHFFFAOYSA-N 0.000 claims 2
- 125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 claims 2
- DXMZNKNJOBUNRO-UHFFFAOYSA-N glycyl radical Chemical compound N[CH]C(O)=O DXMZNKNJOBUNRO-UHFFFAOYSA-N 0.000 claims 2
- 125000000751 azo group Chemical group [*]N=N[*] 0.000 claims 1
- 230000004048 modification Effects 0.000 claims 1
- 238000006011 modification reaction Methods 0.000 claims 1
- 150000003254 radicals Chemical class 0.000 claims 1
- UCGZNHXYVJOCMV-UHFFFAOYSA-N 2-amino-2-(3-aminophenyl)acetic acid Chemical compound OC(=O)C(N)C1=CC=CC(N)=C1 UCGZNHXYVJOCMV-UHFFFAOYSA-N 0.000 description 16
- LSNNMFCWUKXFEE-UHFFFAOYSA-N sulfonic acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 description 10
- DHMQDGOQFOQNFH-UHFFFAOYSA-N glycine Chemical compound NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 description 8
- DKPVORLEZUKTNG-UHFFFAOYSA-N NC=1C(=C(C=CC=1)C)NCC(=O)O Chemical compound NC=1C(=C(C=CC=1)C)NCC(=O)O DKPVORLEZUKTNG-UHFFFAOYSA-N 0.000 description 7
- JBIJLHTVPXGSAM-UHFFFAOYSA-N 2-Naphthylamine Chemical compound C1=CC=CC2=CC(N)=CC=C21 JBIJLHTVPXGSAM-UHFFFAOYSA-N 0.000 description 4
- 239000004471 Glycine Substances 0.000 description 4
- KYARBIJYVGJZLB-UHFFFAOYSA-N 7-amino-4-hydroxy-2-naphthalenesulfonic acid Chemical compound OC1=CC(S(O)(=O)=O)=CC2=CC(N)=CC=C21 KYARBIJYVGJZLB-UHFFFAOYSA-N 0.000 description 3
- 229920000742 Cotton Polymers 0.000 description 3
- 229940018564 M-PHENYLENEDIAMINE Drugs 0.000 description 3
- WZCQRUWWHSTZEM-UHFFFAOYSA-N M-Phenylenediamine Chemical compound NC1=CC=CC(N)=C1 WZCQRUWWHSTZEM-UHFFFAOYSA-N 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- VOZKAJLKRJDJLL-UHFFFAOYSA-N 2,4-Diaminotoluene Chemical compound CC1=CC=C(N)C=C1N VOZKAJLKRJDJLL-UHFFFAOYSA-N 0.000 description 2
- HBZVNWNSRNTWPS-UHFFFAOYSA-N 6-amino-4-hydroxynaphthalene-2-sulfonic acid Chemical compound C1=C(S(O)(=O)=O)C=C(O)C2=CC(N)=CC=C21 HBZVNWNSRNTWPS-UHFFFAOYSA-N 0.000 description 2
- GHMLBKRAJCXXBS-UHFFFAOYSA-N Resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 2
- 230000001808 coupling Effects 0.000 description 2
- 238000010168 coupling process Methods 0.000 description 2
- 238000005859 coupling reaction Methods 0.000 description 2
- 150000008049 diazo compounds Chemical class 0.000 description 2
- IOVCWXUNBOPUCH-UHFFFAOYSA-M nitrite anion Chemical compound [O-]N=O IOVCWXUNBOPUCH-UHFFFAOYSA-M 0.000 description 2
- CWLKGDAVCFYWJK-UHFFFAOYSA-N 3-Aminophenol Chemical compound NC1=CC=CC(O)=C1 CWLKGDAVCFYWJK-UHFFFAOYSA-N 0.000 description 1
- 229940018563 3-aminophenol Drugs 0.000 description 1
- QYFYIOWLBSPSDM-UHFFFAOYSA-N 6-aminonaphthalen-1-ol Chemical compound OC1=CC=CC2=CC(N)=CC=C21 QYFYIOWLBSPSDM-UHFFFAOYSA-N 0.000 description 1
- ZYSOYLBBCYWEMB-UHFFFAOYSA-N 7-aminonaphthalen-1-ol Chemical compound C1=CC=C(O)C2=CC(N)=CC=C21 ZYSOYLBBCYWEMB-UHFFFAOYSA-N 0.000 description 1
- 241000947840 Alteromonadales Species 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-N Carbonic acid Chemical compound OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 description 1
- CBCKQZAAMUWICA-UHFFFAOYSA-N P-Phenylenediamine Chemical compound NC1=CC=C(N)C=C1 CBCKQZAAMUWICA-UHFFFAOYSA-N 0.000 description 1
- 210000002268 Wool Anatomy 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 150000004985 diamines Chemical class 0.000 description 1
- 238000004043 dyeing Methods 0.000 description 1
- NYGZLYXAPMMJTE-UHFFFAOYSA-M metanil yellow Chemical group [Na+].[O-]S(=O)(=O)C1=CC=CC(N=NC=2C=CC(NC=3C=CC=CC=3)=CC=2)=C1 NYGZLYXAPMMJTE-UHFFFAOYSA-M 0.000 description 1
- 238000007127 saponification reaction Methods 0.000 description 1
- VMHLLURERBWHNL-UHFFFAOYSA-M sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 description 1
- 235000017281 sodium acetate Nutrition 0.000 description 1
- 239000001632 sodium acetate 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
- C09B35/00—Disazo and polyazo dyes of the type A<-D->B prepared by diazotising and coupling
- C09B35/36—Trisazo dyes of the type
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| AT43880D AT43880B (de) | 1906-08-10 | 1909-02-26 | Verfahren zur Darstellung von schwarzen Polyazofarbstoffen. |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE206954C true DE206954C (ro) |
Family
ID=469089
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE1906206954D Expired - Lifetime DE206954C (ro) | 1906-08-10 | 1906-08-10 |
Country Status (1)
| Country | Link |
|---|---|
| DE (1) | DE206954C (ro) |
-
1906
- 1906-08-10 DE DE1906206954D patent/DE206954C/de not_active Expired - Lifetime
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE206954C (ro) | ||
| DE229303C (ro) | ||
| DE223558C (ro) | ||
| DE538669C (de) | Verfahren zur Darstellung von Azofarbstoffen | |
| DE842100C (de) | Verfahren zur Herstellung von Polyazofarbstoffen | |
| DE177178C (ro) | ||
| DE198102C (ro) | ||
| DE178803C (ro) | ||
| DE202116C (ro) | ||
| DE929804C (de) | Verfahren zur Herstellung von Polyazofarbstoffen | |
| DE205251C (ro) | ||
| DE202117C (ro) | ||
| DE180147C (ro) | ||
| DE284699C (ro) | ||
| DE634213C (de) | Verfahren zur Herstellung von Azofarbstoffen | |
| DE917633C (de) | Verfahren zur Herstellung neuer Trisazofarbstoffe | |
| DE670432C (de) | Verfahren zur Herstellung von Disazofarbstoffen | |
| DE741468C (de) | Verfahren zur Herstellung von Polyazofarbstoffen | |
| DE693023C (de) | Verfahren zur Herstellung von Polyazofarbstoffen | |
| DE623923C (de) | Verfahren zur Herstellung von Tetrakisazofarbstoffen | |
| DE848677C (de) | Verfahren zur Herstellung von metallisierbaren Polyazofarbstoffen | |
| DE273934C (ro) | ||
| AT101312B (de) | Verfahren zur Darstellung direktziehender Baumwollfarbstoffe. | |
| DE710502C (de) | Verfahren zur Herstellung von Polyazofarbstoffen | |
| DE92469C (ro) |