Oxymorphone HCl (Oxymorphone Hydrochloride) is a potent semi-synthetic opioid analgesic indicated for the management of moderate-to-severe acute and chronic pain. As a premier Active Pharmaceutical Ingredient (API), it is manufactured by Parand Darou Pharmaceutical Company adhering to stringent USP quality standards and utilizing advanced purification and synthesis technologies.
Quality Profile & Assay Purity
Oxymorphone HCl synthesis at Parand Darou is strictly controlled to maintain optimal chemical purity and batch-to-batch consistency. With an active ingredient assay strictly ranging between 97.0% and 102.0% (on a dried basis) and tightly restricted ignition residues (Max. 0.3%), this API provides pharmaceutical manufacturers with unmatched reliability for solid oral and injectable formulations.
Physical Properties & Storage Requirements
Characterized as a white or off-white, odorless crystalline powder, Oxymorphone HCl is freely soluble in water and exhibits high chemical stability under specified environmental conditions. To maintain maximum efficacy and prevent degradation, the material must be stored in tight, light-resistant containers under controlled room temperature conditions.
General Information
| Product Name | Oxymorphone HCl | |
| Chemical Name | 4,5α-Epoxy-3,14-dihydroxy-17-methylmorphinan-6-one hydrochloride | |
| Manufacturer | Parand Darou Co. | |
| CAS No. | 357-07-3 | |
| Category | Pain management | |
| Pharmacopoeia | USP |
Specification
| Molecular formula | C17H19NO4·HCl | Content of chloride | 10.2%–10.8% on the dried basis | |||
| Molecular weight | 337.8 | Residue on ignition | Max. 0.3% | |||
| Appearance | White or slightly off-white, odorless powder | Assay | 97.0% to 102.0% (dried basis) | |||
| Solubility | Freely soluble in water; sparingly soluble in alcohol and in ether | Storage | Preserve in tight, light-resistant containers. | |||
| Water | Max. 8.0% |
