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Butaclamol CAS NO 36504-93-5


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CAS No.:36504-93-5

Grade:Pharmacy Grade

Content:99.9%

Brand:Customizable

Packaging:Customizable

Description

Butaclamol CAS NO 36504-93-5 is a potent, high-purity chemical compound belonging to the class of antipsychotic agents. It serves as a critical reference standard and active pharmaceutical ingredient (API) for research and development in neuropharmacology. This compound is essential for pharmaceutical manufacturers, analytical laboratories, and research institutions focused on central nervous system (CNS) drug discovery and quality control.

Application

  • Pharmaceutical Reference Standard: Used as a certified standard for analytical method development, validation, and quality control testing of antipsychotic medications.
  • Neuropharmacological Research: A key tool in preclinical studies investigating dopamine receptor interactions and the mechanisms of antipsychotic action.
  • Active Pharmaceutical Ingredient (API): Serves as a crucial intermediate or raw material in the synthesis and formulation of specialized neuropsychiatric drugs.
  • Biochemical Assay Development: Employed in the creation of high-throughput screening assays to identify and characterize novel CNS-targeting compounds.
  • Academic and Clinical Research: Supports fundamental and applied research in universities and hospitals studying schizophrenia and related disorders.

Basic Information

Product Name Butaclamol
CAS No. 36504-93-5
Molecular Formula C25H31NO
Molecular Weight 361.52 g/mol
Synonyms Butaclamol; (+)-Butaclamol; (3aR,4S,4aR,5aS,6R,10bS,11aS)-4-[4-(4-Fluorophenyl)-4-oxobutyl]-3a,4,4a,5,5a,6,7,11,11a,12-decahydro-1H-6,10b-(epiminoethano)naphth[2,1-g]quinoline; 1H-Naphth[2,1-g]quinoline, 4-[4-(4-fluorophenyl)-4-oxobutyl]decahydro-3a,4,8,8-tetramethyl-, (3aR,4S,4aR,5aS,6R,10bS,11aS)-rel-; AY-23,028; NSC 339024
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Quality Control

Our Butaclamol is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing, including HPLC for purity, IR and NMR for structural confirmation, and stringent control of residual solvents and impurities to meet pharmaceutical-grade standards. A detailed Certificate of Analysis (COA) is provided with every shipment to ensure traceability and compliance with your research or manufacturing requirements.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at a controlled room temperature (15-25°C). Due to its hygroscopic nature, the container must be kept tightly sealed in a dry environment to prevent moisture absorption, which can affect stability and purity.

Specification

Item Specification
Appearance White to off-white crystalline powder
Identification (IR) Conforms to reference spectrum
Identification (HPLC) Retention time matches reference standard
Purity (HPLC) ≥ 98.0%
Loss on Drying ≤ 0.5%
Residue on Ignition ≤ 0.1%
Heavy Metals ≤ 20 ppm
Residual Solvents (GC) Complies with ICH Q3C guidelines

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

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Each batch undergoes strict QC, accompanied by COA, MSDS, and full compliance with international standards.

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