DE248999C - - Google Patents
Info
- Publication number
- DE248999C DE248999C DENDAT248999D DE248999DA DE248999C DE 248999 C DE248999 C DE 248999C DE NDAT248999 D DENDAT248999 D DE NDAT248999D DE 248999D A DE248999D A DE 248999DA DE 248999 C DE248999 C DE 248999C
- Authority
- DE
- Germany
- Prior art keywords
- orange
- copper
- dibromo
- dye
- vat
- 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
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims description 5
- 229910052802 copper Inorganic materials 0.000 claims description 4
- 239000010949 copper Substances 0.000 claims description 4
- 239000007859 condensation product Substances 0.000 claims description 2
- 239000000984 vat dye Substances 0.000 claims description 2
- 125000002485 formyl group Chemical class [H]C(*)=O 0.000 claims 2
- 239000002253 acid Substances 0.000 claims 1
- 150000007513 acids Chemical class 0.000 claims 1
- 150000001454 anthracenes Chemical class 0.000 claims 1
- 125000000649 benzylidene group Chemical group [H]C(=[*])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 claims 1
- 238000000034 method Methods 0.000 claims 1
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 9
- HUMNYLRZRPPJDN-UHFFFAOYSA-N benzaldehyde Chemical compound O=CC1=CC=CC=C1 HUMNYLRZRPPJDN-UHFFFAOYSA-N 0.000 description 6
- -1 benzylidene compound Chemical class 0.000 description 4
- 239000000975 dye Substances 0.000 description 4
- 239000002184 metal Substances 0.000 description 4
- 229910052751 metal Inorganic materials 0.000 description 4
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 4
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- QNGNSVIICDLXHT-UHFFFAOYSA-N para-ethylbenzaldehyde Natural products CCC1=CC=C(C=O)C=C1 QNGNSVIICDLXHT-UHFFFAOYSA-N 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- 150000001299 aldehydes Chemical group 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 239000013078 crystal Substances 0.000 description 2
- 239000000155 melt Substances 0.000 description 2
- LQNUZADURLCDLV-UHFFFAOYSA-N nitrobenzene Chemical compound [O-][N+](=O)C1=CC=CC=C1 LQNUZADURLCDLV-UHFFFAOYSA-N 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 229920000742 Cotton Polymers 0.000 description 1
- 229960000583 acetic acid Drugs 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 239000012043 crude product Substances 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- GRWZHXKQBITJKP-UHFFFAOYSA-N dithionous acid Chemical compound OS(=O)S(O)=O GRWZHXKQBITJKP-UHFFFAOYSA-N 0.000 description 1
- 238000004043 dyeing Methods 0.000 description 1
- 239000012362 glacial acetic acid Substances 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 239000002932 luster Substances 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000010298 pulverizing process Methods 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 235000011121 sodium hydroxide Nutrition 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 238000010792 warming Methods 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
- C09B5/00—Dyes with an anthracene nucleus condensed with one or more heterocyclic rings with or without carbocyclic rings
- C09B5/02—Dyes with an anthracene nucleus condensed with one or more heterocyclic rings with or without carbocyclic rings the heterocyclic ring being only condensed in peri position
- C09B5/20—Flavanthrones
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE248999C true DE248999C (cs) |
Family
ID=507659
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DENDAT248999D Active DE248999C (cs) |
Country Status (1)
| Country | Link |
|---|---|
| DE (1) | DE248999C (cs) |
-
0
- DE DENDAT248999D patent/DE248999C/de active Active
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE248999C (cs) | ||
| DE238982C (cs) | ||
| DE455280C (de) | Verfahren zur Herstellung indigoider Farbstoffe und deren Zwischenprodukte | |
| DE248169C (cs) | ||
| DE745465C (de) | Verfahren zur Herstellung von Phthalocyaninfarbstoffen | |
| DE628150C (de) | Verfahren zur Herstellung von Kuepenfarbstoffen | |
| DE239544C (cs) | ||
| DE262469C (cs) | ||
| DE254743C (cs) | ||
| AT55728B (de) | Verfahren zur Darstellung von schwefelhaltigen Küpenfarbstoffen der Anthrazenreihe. | |
| DE280840C (cs) | ||
| DE66611C (de) | Verfahren zur Darstellung eines beizenziehenden Farbstoffs aus Perchlornaphtalin | |
| DE252839C (cs) | ||
| DE518335C (de) | Verfahren zur Darstellung von Abkoemmlingen der Benzanthronpyrazolanthronreihe | |
| DE290064C (cs) | ||
| DE234749C (cs) | ||
| DE251845C (cs) | ||
| DE491429C (de) | Verfahren zur Darstellung von Kuepenfarbstoffen | |
| DE573556C (de) | Verfahren zur Darstellung von 1, 9-Anthrapyrimidinen | |
| DE495975C (de) | Verfahren zur Herstellung von Kuepenfarbstoffen der Anthrachinonacridonreihe | |
| DE524362C (de) | Verfahren zur Herstellung von Kuepenfarbstoffen | |
| DE81245C (cs) | ||
| DE541265C (de) | Verfahren zur Darstellung stickstoffhaltiger Kondensationsprodukte | |
| DE67115C (de) | Verfahren und Darstellung von o-Tolylrosindulin | |
| DE190292C (cs) |