Products Description
As an advantageous framework in medicinal chemistry, its derivatives exhibit a wide range of biological activities such as anti-malaria, anti-viral, anti-bacterial, and anti-tumor properties, and hold significant importance in new drug development and the optimization of lead compounds.
Its rigid planar tricyclic structure endows the molecule with excellent thermal stability and chemical stability. At the same time, it possesses characteristic blue fluorescence and n-π* electronic transition ability, making it of unique value in the field of optical materials.
Products Specification
| Product name | 9(10H)-ACRIDONE |
| CAS NO | 578-95-0 |
| ITEM NO | M590 |
| Appearance | Yellow crystalline powder |
| Purity | 99% |
| Loss of mass on drying | 0.10% |
| Mass fraction of chlorides | ≤0.3 % |
| Mass fraction of sulfate | ≤0.7 % |
| Melting Point | 363.3°C |
| Package | 100g/1kg/10kg etc. |
| Delivery | 2-3days |
| Storage | room temperature |
| MSDS/COA/TDS | Connect us |
Products Application
1. Organic synthesis intermediates: Used for the preparation of acridine derivatives and other functional materials.
2.Drug impurity analysis and standards: Used as impurity standards for drugs such as oxacillin.
2. Pharmaceutical organic synthesis intermediates: Synthesis of small molecule candidate drugs for anti-tumor, anti-viral, anti-malarial/anti-parasitic, and antibacterial purposes; planar structures can be combined with DNA insertion for new drug structure-activity relationship research.
3. Research materials field: Fluorescent probes, biological fluorescence labeling; synthesis blocks of OLED organic photonic materials, functional dyes.
FAQ
Q: What solvent is suitable for dissolving acridone in the experiment?
A: Hardly soluble in cold water. Hot DMSO, hot acetic acid or hot ethanol is recommended.
Q: Will it degrade under light exposure?
A: Light‑sensitive. Keep away from light during storage and experiment to avoid degradation.
Q: What kinds of derivatives can be synthesized from acridone?
A: Mainly for N‑alkylation and halogenation derivatives for anti‑tumor, antibacterial candidates and fluorescent molecules.
Q: What features for organic optoelectronic research?
A: Tricyclic conjugated structure with blue fluorescence, good building block for luminescent & fluorescent sensor materials.
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