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Indeloxazine Hydrochloride CAS NO 65043-22-3


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CAS No.:65043-22-3

Grade:Pharmacy Grade

Content:99.9%

Brand:Customizable

Packaging:Customizable

Description

Indeloxazine Hydrochloride is a high-purity organic compound with significant pharmacological interest. This compound is valued for its role as a key intermediate or active pharmaceutical ingredient (API) in advanced neurological and psychiatric research. It is primarily utilized by pharmaceutical R&D departments, contract research organizations (CROs), and fine chemical manufacturers targeting the central nervous system (CNS) therapeutic area. Our supply ensures consistent quality and reliability for critical development and production processes.

Application

  • Pharmaceutical Intermediate: Serves as a critical building block in the synthesis of novel neuroactive drugs and investigational compounds.
  • Neurological Research: Used in preclinical and clinical research studies focusing on cognitive function and neurological pathways.
  • Active Pharmaceutical Ingredient (API): Employed in the formulation development of prescription medications targeting specific CNS disorders.
  • Reference Standard: Acts as a high-purity analytical standard for quality control and method validation in pharmaceutical laboratories.
  • Biochemical Research: Utilized in studies investigating receptor binding and enzymatic activity related to brain function.
  • Contract Manufacturing: Supplied to CDMOs (Contract Development and Manufacturing Organizations) for cGMP-compliant production runs.

Basic Information

Product Name Indeloxazine Hydrochloride
CAS No. 65043-22-3
Molecular Formula C16H22N2O2•HCl
Molecular Weight 310.82 g/mol
Synonyms 2-[(1H-Indol-3-yl)methyl]-4-morpholinyl 1-piperazinecarboxylate hydrochloride; Y-8894; Elen; Indeloxazine HCl; 1-Piperazinecarboxylic acid, 2-[(1H-indol-3-yl)methyl]-4-morpholinyl ester, hydrochloride
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Quality Control

Our Indeloxazine Hydrochloride is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing, including HPLC for purity, residual solvent analysis, and identity confirmation (IR, NMR) to ensure it meets stringent specifications for pharmaceutical use. Certificates of Analysis (COA) documenting all test results are provided with every shipment to support your regulatory and quality assurance requirements.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated area at a controlled room temperature (15-25°C). Due to its hygroscopic nature, the container must be kept tightly sealed to minimize exposure to atmospheric moisture.

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) ≥98.5%
Related Substances (HPLC) Total impurities ≤1.5%
Water Content (KF) ≤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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With our own production facilities, we ensure consistent quality, reliable supply, and full traceability.

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

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Our in-house lab drives process innovation, new product development, and tailored synthesis solutions.