Description
IUPAC Name: 1-(2-hydroxy-4-methoxyphenyl)ethanone
InChI: InChI=1S/C9H10O3/c1-6(10)8-4-3-7(12-2)5-9(8)11/h3-5,11H,1-2H3
InChIKey: UILPJVPSNHJFIK-UHFFFAOYSA-N
Canonical SMILES: CC(=O)C1=C(C=C(C=C1)OC)O
Isomeric SMILES: CC(=O)C1=C(C=C(C=C1)OC)O
Synonyms: PAEONOL; 552-41-0; 2′-Hydroxy-4′-methoxyacetophenone; 1-(2-Hydroxy-4-methoxyphenyl)ethanone; Peonol; 2-Hydroxy-4-methoxyacetophenone; Ethanone, 1-(2-hydroxy-4-methoxyphenyl)-; 1-(2-hydroxy-4-methoxyphenyl)ethan-1-one; …
Botanical Source: Paeonia suffruticosa Andr.
Product Overview
High-purity Paeonol (2′-Hydroxy-4′-methoxyacetophenone), a natural phenolic compound isolated from Paeonia suffruticosa and Paeonia lactiflora, manufactured to exceptional standards for pharmaceutical and biomedical research.
Technical Specifications
- Molecular Formula: C₉H₁₀O₃
- Molecular Weight: 166.17 g/mol
- Purity: ≥98% (HPLC)
- Appearance: White to off-white crystalline powder
- Solubility: Soluble in DMSO, ethanol; poorly soluble in water
Key Features & Benefits
- Natural phenolic compound
- Anti-inflammatory properties
- Validated structure and activity
- Comprehensive Certificate of Analysis
- Full spectroscopic characterization
Research Applications
-
Inflammation Research
- NF-κB pathway studies
- Cytokine modulation research
- Anti-inflammatory mechanisms
- Immune response investigations
-
Pharmaceutical Development
- Cardiovascular research
- Neuroprotection studies
- Pain management research
- Drug discovery screening
-
Mechanism Studies
- Cell signaling pathways
- Oxidative stress research
- Apoptosis mechanisms
- Molecular target identification
Storage & Handling
- Store at -20°C
- Protect from light and moisture
- Avoid repeated freeze-thaw cycles
- Stock solution guidelines provided
- 24-month stability under recommended conditions
Quality Assurance
- GMP-compliant manufacturing
- Rigorous quality control
- Complete analytical documentation
- Traceable lot numbers
- Stability monitoring program
Research Support
BIORLAB provides:
- Technical consultation
- Analytical method support
- Stability data
- Custom synthesis options
- Application Guidance
Key Research Areas
-
Anti-inflammatory Effects
- Pro-inflammatory mediators
- COX-2 expression
- NF-κB signaling
- Inflammatory cytokines
-
Cardiovascular Protection
- Endothelial function
- Vascular inflammation
- Atherosclerosis research
- Platelet aggregation
-
Neuroprotection
- Oxidative stress
- Neuroinflammation
- Neural cell protection
- Pain modulation
This premium-grade Paeonol is specifically designed for research institutions and pharmaceutical companies advancing therapeutic development and scientific research.
For research and development purposes only. Not for human consumption or clinical use.
[Contact BIORLAB’s technical support team for detailed specifications and custom requirements]