Description

Butaperazine Maleate is a high-purity pharmaceutical intermediate and active compound. It serves as a critical building block in the synthesis of advanced therapeutic agents, requiring stringent quality control for efficacy and safety. This compound is essential for research institutions and pharmaceutical manufacturers developing and producing neuroleptic medications. We supply it globally to meet the exacting standards of the pharmaceutical and fine chemical industries.

Application

• Pharmaceutical Active Ingredient (API): Primary use as a key component in the formulation of antipsychotic medications.
• Research & Development: Utilized in biochemical and pharmacological studies to investigate neurological pathways and receptor interactions.
• Reference Standard: Serves as a certified reference material (CRM) for analytical method development and quality control testing in laboratories.
• Fine Chemical Synthesis: Acts as a sophisticated intermediate in the multi-step synthesis of complex organic molecules and novel drug candidates.

Basic Information

Product Name	Butaperazine Maleate
CAS No.	10213-91-9
Molecular Formula	C₂₄H₃₀N₃O₂S⁺·C₄H₃O₄⁻
Molecular Weight	523.62 g/mol
Synonyms	Butaperazine Maleate; Butaperazinium Maleate; 1-[10-[3-(4-Methylpiperazin-1-yl)propyl]-10H-phenothiazin-2-yl]propan-1-one Maleate; Riker 595; Butyrylperazine Maleate; Butaperazine Hydrogen Maleate; Butaperazini Maleas
EINECS	Contact for details

Quality Control

Our Butaperazine Maleate is manufactured under a GMP-compliant quality management system. Each batch undergoes comprehensive analytical testing, including identity confirmation, purity assay, and impurity profiling, to ensure it meets stringent pharmaceutical-grade specifications. A detailed Certificate of Analysis (COA) is provided with every shipment, and we support audits and regulatory documentation requirements.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at a controlled room temperature (typically 15-25°C). The product is light-sensitive and should be handled and stored accordingly to maintain stability.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to reference spectrum
Identification (HPLC)	Retention time matches reference standard
Assay (HPLC)	≥ 98.0%
Related Substances (HPLC)	Total impurities ≤ 2.0% Any single impurity ≤ 0.5%
Loss on Drying	≤ 1.0%
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.