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Loxapine Hydrochloride CAS NO 54810-23-0
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CAS No.:54810-23-0
Grade:Pharmacy Grade
Content:99.9%
Brand:Customizable
Packaging:Customizable
Description
Loxapine Hydrochloride is a high-purity pharmaceutical active ingredient, a dibenzoxazepine antipsychotic agent. It is a critical intermediate and active pharmaceutical ingredient (API) for the formulation of antipsychotic medications. This compound is essential for pharmaceutical manufacturers and research institutions developing treatments for schizophrenia and other related psychiatric disorders. Our supply ensures consistent quality and reliable availability for global pharmaceutical production.
Application
- Primary Active Pharmaceutical Ingredient (API) in the manufacture of antipsychotic medications.
- Key intermediate in the synthesis of final dosage forms, such as tablets and capsules.
- Reference standard for analytical method development and quality control in pharmaceutical laboratories.
- Raw material for research and development of novel neuropsychiatric therapeutics.
- Used in clinical studies and pharmacological research.
- Essential component for compounding pharmacies requiring specific formulations.
Basic Information
| Product Name | Loxapine Hydrochloride |
| CAS No. | 54810-23-0 |
| Molecular Formula | C18H19ClN2O • HCl |
| Molecular Weight | 355.27 g/mol |
| Synonyms | Loxapine HCl; 2-Chloro-11-(4-methyl-1-piperazinyl)dibenz[b,f][1,4]oxazepine hydrochloride; Loxapine monohydrochloride; CL-71563; Loxitane (brand name derivative); Sumitomo Loxapine; Oxilapine Hydrochloride; Dibenzo[b,f][1,4]oxazepine, 2-chloro-11-(4-methyl-1-piperazinyl)-, monohydrochloride |
| EINECS | 259-342-5 |
Quality Control
Our Loxapine Hydrochloride is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing to ensure it meets stringent specifications for pharmaceutical use, including identity, purity, and impurity profiles. A Certificate of Analysis (COA) is provided with each shipment, detailing results against relevant pharmacopeial standards (such as USP/EP) and in-house specifications.
Storage
Preserve in a tightly closed container, protected from light. Store in a cool, dry place at controlled room temperature (15-25°C). This product is hygroscopic (moisture-sensitive) and must be kept in a dry environment to prevent degradation. For long-term storage, consider desiccants or inert atmosphere packaging.
Specification
| Item | Specification |
|---|---|
| Appearance | White to off-white crystalline powder |
| Identification (IR) | Conforms to reference standard |
| Identification (HPLC) | Retention time matches reference |
| Assay (HPLC) | 98.0% - 102.0% (on anhydrous basis) |
| Water Content (KF) | ≤ 0.5% |
| Residue on Ignition | ≤ 0.1% |
| Heavy Metals | ≤ 20 ppm |
| Related Substances (HPLC) | Individual impurity ≤ 0.5%; Total impurities ≤ 1.5% |
| Specific Optical Rotation | Contact for details |
Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.
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Why choose US
Trusted Manufacturer
With our own production facilities, we ensure consistent quality, reliable supply, and full traceability.
Rigorous Quality Assurance
Each batch undergoes strict QC, accompanied by COA, MSDS, and full compliance with international standards.
Advanced R&D Expertise
Our in-house lab drives process innovation, new product development, and tailored synthesis solutions.






