HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,5-Dianilinoterephthalic acid → Quinacridone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,5-Dianilinoterephthalic acid | HCID 82351 | — |
| Reactant | HCID 18377742 | HCID 18377742 | — |
| Product | Quinacridone | HCID 13976 | — |
Reaction Steps
Pigmentary quinacridone was prepared exactly as described in comparison Example 2 except that 10% by weight, relative to the 2,5-dianilinoterephthalic acid, of 2,5-di(sulfamoylanilino)terephthalic acid (6 g) was included in the ring-closure reaction. Quinacridone (50.2 g) was obtained as a violet pigment.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05755873 |
| Source dataset | uspto-grants-1998_05 |
| ORD ID | ord-c0f7930393c3492e8ce4258cb7a82421 |
| Source note | uspto-grants-1998_05 |