Description

Vedaclidine CAS NO 141593-42-2 is a high-purity pharmaceutical intermediate and research chemical of significant interest in medicinal chemistry. This compound is primarily valued for its role as a key building block in the synthesis of novel active pharmaceutical ingredients (APIs) targeting neurological pathways. It is essential for research institutions, pharmaceutical R&D departments, and fine chemical manufacturers engaged in the development of advanced therapeutic agents. Our supply ensures consistent quality and reliable availability for critical development and production processes.

Application

• Pharmaceutical Intermediate: A critical precursor in the multi-step synthesis of complex drug candidates, particularly in central nervous system (CNS) research.
• Medicinal Chemistry Research: Serves as a versatile scaffold or building block for designing and optimizing new molecular entities in drug discovery programs.
• Reference Standard: Used as an analytical standard in quality control laboratories for method development, validation, and impurity profiling.
• Biochemical Research: Employed in in-vitro studies to investigate specific biological activities and receptor interactions.
• Process Development: Utilized in scaling up synthetic routes from laboratory to pilot plant and commercial manufacturing scales.
• Contract Manufacturing: Supplied to CDMOs (Contract Development and Manufacturing Organizations) for the production of client-specific compounds and APIs.

Basic Information

Product Name	Vedaclidine
CAS No.	141593-42-2
Molecular Formula	C19H24N2O2
Molecular Weight	312.41 g/mol
Synonyms	Vedaclidine; (3R)-1-Azabicyclo[2.2.2]oct-3-yl (1S)-1-phenyl-3,4-dihydro-1H-isoquinoline-2-carboxylate; (R)-Quinuclidin-3-yl (1S)-1-phenyl-3,4-dihydroisoquinoline-2(1H)-carboxylate; (R)-3-Quinuclidinol (1S)-1-phenyl-1,2,3,4-tetrahydroisoquinoline-2-carboxylate; 141593-42-2; Vedaclidine (USAN); USAN Vedaclidine; Vedaclidine [USAN]
EINECS	Contact for details

Quality Control

Our Vedaclidine is manufactured under a strict quality management system. Every batch undergoes comprehensive analytical testing, including HPLC for purity and assay, identification by spectroscopic methods (IR, NMR), and control of specified impurities. We provide a detailed Certificate of Analysis (COA) with each shipment, ensuring full traceability and compliance with your research or cGMP (current Good Manufacturing Practice) requirements for pharmaceutical intermediates.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated place 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. For long-term storage, consider using desiccants.

Specification

Item	Specification
Appearance	White to off-white 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%
Water Content (KF)	≤ 1.0%
Residue on Ignition	≤ 0.1%

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