| Parameter | Value |
| Material | DL-Synephrine |
| CAS Number | 94-07-5 |
| Molecular Formula | C9H13NO2 |
| Purity | ≥98% |
| Appearance | Colorless Crystals |
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DL-Synephrine Powder is a dual-isomer bioactive Citrus alkaloid standardized to ≥98% purity. It functions as a selective α1-adrenergic receptor agonist (EC50 = 8.2 μM) to promote lipolysis and thermogenesis without significant β-adrenergic effects. Clinically validated for safe use at a dose of ≤100mg/day, it is formulated for thermogenic fat-burning applications that require precise modulation of adrenergic activity. This biogenic amine features:
Structural Characteristics
Quality Specifications
Pharmacological Activity
Properties
| Property | Value |
| Material | DL-Synephrine |
| CAS Number | 94-07-5 |
| Molecular Formula | C9H13NO2 |
| Purity | ≥98% |
| Appearance | Colorless Crystals |
| Molecular Weight | 167.207 |
| Melting Point | 187°C |
| Boiling Point | 341.1°C at 760 mmHg |
*The above product information is based on theoretical data. For specific requirements and detailed inquiries, please contact us.
1. Nutraceuticals
2. Pharmaceuticals
3. Cosmetics
4. Analytical Standards
5. Sports Nutrition
Q1. How does DL-Synephrine differ from natural synephrine in weight management products?
DL-Synephrine is a synthetic racemic mixture providing consistent α1-adrenergic receptor activation (EC50=8.2μM), whereas natural citrus extracts vary in D/L isomer ratios. Its standardized melting point (184-187°C) and ≥98% HPLC purity ensure batch-to-batch reproducibility in thermogenic formulations.
Q2. What analytical methods confirm DL-Synephrine purity in bulk supplements?
Reverse-phase HPLC with methanol-water gradients (65:35 v/v) is mandatory, detecting the primary peak at 6.3±0.2 minutes retention time. Complementary FTIR validation should show characteristic phenolic C-O stretch at 1240 cm⁻¹ and absence of solvent residues below 500 ppm.
Q3. Why is DL-Synephrine preferred over ephedrine in pharmaceutical research?
DL-Synephrine exhibits selective α1-agonism without significant β-adrenergic activity, minimizing cardiovascular side effects. Its orthorhombic crystal structure enhances stability during in vitro assays, and thermal decomposition initiates only above 85°C.