
Levodopa is a premium-grade, white crystalline aromatic amino acid powder compound carrying CAS number 59-92-7. Processed under strict pharmaceutical compliance, this high-purity central nervous system agent exhibits exceptional metabolic transformation profiles and uniform matrix solubility, making it an ideal core choice for manufacturing clinical tablets, standard oral capsules, and advanced neuro-chemical research formulations globally.
Excellent crystalline dissolution behavior and outstanding blood-brain tissue permeability profiles provide a distinct operational edge when engineering modern fast-acting neurological formulations. This active pharmaceutical solid operates by successfully crossing protective vascular boundaries before converting into active dopamine via enzymatic pathways, supplying the exact biological mechanisms required to support motor balance without altering raw binder uniformity. It assists compounding engineers in maintaining strict dosage uniformity across high-speed encapsulation runs, mitigating trace separation risks within automated volumetric feeding systems. For instance, specialized pharmaceutical facilities incorporate this chiral amino acid derivative as a core active component in targeted neurological tablet lines. As a consequence, it maximizes the technical throughput of automated filling machinery and continuous quality assurance checks. Consequently, Zyntex coordinates clean room crystallization paths to eliminate downstream polymorph shifts from your factory schedule.
In addition to this, Zyntex coordinates climate-controlled logistics for pilot-scale trials and advanced central nervous system formulation research centers. The compound maintains its refined crystalline integrity under strict storage parameters, preventing heat-induced polymorph changes or chemical breakdown during automated mechanical blending steps. It advances contemporary medical engineering by providing a thoroughly analyzed, highly predictable metabolic raw material that meets international monograph standards. Simultaneously, it remains a critical chemical standard for routine high-performance liquid chromatography (HPLC) calibrations and bioanalytical validation testing assays. In brief, our product functions as a dependable chemical foundation, supporting both the performance of commercial tablet batches and the analytical rigor of specialized industrial laboratories.
This high-purity crystalline active drug compound delivers crucial technical value within these four primary industrial sectors:
Primary active pharmaceutical source used for compressing uniform, clinical-grade oral neurological tablets and release matrices. Hence, it directly supports optimal dosage control lines.
Utilized as a high-purity active hammadde base to pack hard-shell oral capsules and multi-component therapeutic formulas. Clearly, it is key for uniform dissolving patterns.
Acts as an essential reference active standard for chiral purity metrics, assay calibration, and routine laboratory diagnostics. Resultantly, it guarantees excellent matrix clarity.
Used as a professional active component for engineering advanced blood-tissue barrier models and specialized liposomal drug carriers. Specifically, it confirms optimal reaction pathways.
| Parameter | Standard Value |
|---|---|
| Product Name | Levodopa (L-DOPA) |
| Assay / Purity (HPLC) | 99.0% to 101.0% (Dry Basis) |
| Appearance | White or almost white crystalline powder |
| Specific Rotation | -160° to -167° |
| Solubility | Slightly soluble in water; practically insoluble in ethanol; freely soluble in dilute HCl |
| CAS Number | 59-92-7 |
📝 Safety & Handling: Levodopa is a highly potent neuro-active pharmaceutical hammadde. Direct inhalation of crystalline bulk powder dust or accidental eye/skin exposure can trigger neurological balance adjustments, temporary physiological shifts, and acute respiratory tract mucosal irritation. Therefore, store strictly inside original airtight industrial containers within a well-ventilated, remarkably dry warehouse zone protected from light, moisture, oxygen exposure, and elevated temperatures. Prevent airborne dust clouds during dispensing loops. Proper personal protective equipment (PPE)—including chemical-resistant nitrile gloves, safety glasses with side shields, and a certified dust respirator mask—must be worn during all manufacturing handling phases. Review the Safety Data Sheet (SDS).