| Parameter | Value |
| Material | Artemisinic Acid |
| CAS Number | 80286-58-4 |
| Molecular Formula | C15H22O2 |
| Purity | ≥98% (HPLC) |
| Appearance | Colorless Crystal |
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Artemisinic Acid Powder (CAS No. 80286-58-4) is a white crystalline sesquiterpene compound naturally abundant in Artemisia annua (sweet wormwood). Serving as the key biosynthetic precursor to artemisinin, it features a characteristic peroxide-free structure with a carboxylic acid functional group. Industrially valued for its role in semi-synthetic artemisinin production, it also exhibits intrinsic anti-inflammatory and antimicrobial bioactivity.
Physicochemical Properties
Stability & Handling
Spectroscopic Data
| Technique | Key Identifiers |
| UV-Vis | λ<sub>max</sub> 210 nm, 260 nm |
| FTIR | 3200 cm⁻¹ (O–H), 1700 cm⁻¹ (C=O), 1640 cm⁻¹ (C=C) |
Properties
| Property | Value |
| Material | Artemisinic Acid |
| CAS No. | 80286-58-4 |
| Molecular Formula | C15H22O2 |
| Purity | ≥98% (HPLC) |
| Appearance | Colorless Crystal |
| Melting Point | 129-131°C |
| Boiling Point | 373.6°C at 760 mmHg |
*The above product information is based on theoretical data. For specific requirements and detailed inquiries, please contact us.
1. Pharmaceutical Manufacturing
2. Cosmetics & Skincare
3. Agricultural Solutions
4. Materials Science
5. Industrial Biotechnology
6. Veterinary Medicine
7. Research Applications
Q1. What are its core properties?
The powder melts at 142–145°C and decomposes above 200°C. It dissolves in polar solvents (methanol, ethanol, DMSO) but not in water or hexane. Its structure includes conjugated double bonds sensitive to light/oxidation, causing yellowing upon air exposure. Infrared spectra show carbonyl (1700 cm⁻¹) and carboxylic hydroxyl (3200 cm⁻¹) peaks.
Q2. Is it safe?
Handling requires caution: May cause eye/skin irritation. Ingestion risks include nausea and dizziness. No severe toxicity reported at industrial exposure levels, but avoid inhalation. Not evaluated for pregnancy use. Store away from oxidizers.
Q3. How does it differ from artemisinin?
Artemisinic acid lacks artemisinin’s endoperoxide bridge, making it non-antimalarial but more stable. It serves as the direct chemical precursor; conversion to artemisinin requires photo-oxidation or enzymatic steps.