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Loxapine CAS NO 1977-10-2


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CAS No.:1977-10-2

Grade:Pharmacy Grade

Content:99.9%

Brand:Customizable

Packaging:Customizable

Description

Loxapine CAS NO 1977-10-2 is a dibenzoxazepine-class tricyclic compound primarily recognized for its antipsychotic properties. It is a critical active pharmaceutical ingredient (API) used in the formulation of medications for the management of schizophrenia and other psychotic disorders. This high-purity compound is essential for pharmaceutical manufacturers and research institutions focused on central nervous system therapeutics. Our supply ensures consistent quality and reliable availability for global production and development needs.

Application

  • Primary use as an Active Pharmaceutical Ingredient (API) in the manufacture of antipsychotic medications.
  • Formulation of oral dosage forms such as tablets and capsules for the treatment of schizophrenia.
  • Research and development of novel drug delivery systems, including potential inhalation powders.
  • Chemical reference standard for analytical testing and quality control in pharmaceutical laboratories.
  • Preclinical and clinical research studies investigating neurological pathways and drug efficacy.
  • Starting material or intermediate in the synthesis of more complex pharmaceutical compounds.

Basic Information

Product Name Loxapine
CAS No. 1977-10-2
Molecular Formula C18H18ClN3O
Molecular Weight 327.81 g/mol
Synonyms Loxapine; Loxapine Base; 2-Chloro-11-(4-methyl-1-piperazinyl)dibenz[b,f][1,4]oxazepine; Oxilapine; CL-71563; Loxapac; Loxitane; Sumilap; Daxolin; Desconex; Loxapin; Loxapinum
EINECS 217-852-9

Quality Control

Our Loxapine is manufactured under strict quality management systems to meet the rigorous standards of the pharmaceutical industry. Every batch is subjected to comprehensive analytical testing, including identification, purity assay, and impurity profiling via advanced techniques like HPLC. A Certificate of Analysis (COA) is provided with each shipment, detailing compliance with in-house specifications. We support compliance with major pharmacopeial guidelines (e.g., USP, EP) and regulatory frameworks such as ICH Q7.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated area at controlled room temperature (typically 15-25°C). Keep away from incompatible materials. The container should be kept tightly sealed to protect from moisture.

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)
Related Substances (HPLC) Individual impurity ≤ 0.5%; Total impurities ≤ 1.5%
Loss on Drying ≤ 0.5%
Residue on Ignition ≤ 0.1%
Heavy Metals ≤ 20 ppm

Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.

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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.