Description

Edivoxetine CAS NO 1194508-25-2 is a selective norepinephrine reuptake inhibitor (NRI) of significant interest in pharmaceutical research and development. Its primary value lies in its targeted mechanism of action, which is crucial for investigating treatments for central nervous system disorders. This compound is essential for pharmaceutical companies, research institutions, and contract development and manufacturing organizations (CDMOs) focused on neuropharmacology and novel therapeutic agents.

Application

• Pharmaceutical Intermediate: Serves as a key building block in the synthesis of advanced active pharmaceutical ingredients (APIs) targeting neurological pathways.
• Neuropharmacology Research: Used as a reference standard and investigational compound in preclinical and clinical studies for mood and attention disorders.
• Mechanistic Studies: Employed in biochemical assays to study norepinephrine transporter (NET) inhibition and its physiological effects.
• Drug Discovery & Development: A critical material in high-throughput screening and lead optimization programs for CNS-targeted therapies.
• Analytical Reference Standard: Provides a certified standard for quality control and analytical method development (HPLC, LC-MS) in pharmaceutical manufacturing.
• Academic Research: Utilized in university and institutional labs for fundamental neuroscience and medicinal chemistry research.

Basic Information

Product Name	Edivoxetine
CAS No.	1194508-25-2
Molecular Formula	C17H21NO3
Molecular Weight	287.35 g/mol
Synonyms	(R)-Edivoxetine; (R)-N-Methyl-3-(2-methylphenoxy)-3-phenylpropan-1-amine; LY2216684; (R)-LY2216684; (3R)-3-(2-Methylphenoxy)-3-phenyl-N-methylpropan-1-amine; (R)-N-Methyl-3-phenyl-3-(o-tolyloxy)propan-1-amine; (R)-3-(2-Methylphenoxy)-3-phenyl-N-methylpropylamine
EINECS	Contact for details

Quality Control

Our Edivoxetine is manufactured under strict quality management systems to ensure batch-to-batch consistency and high purity. Each lot is supported by a comprehensive Certificate of Analysis (COA) detailing identity, purity, and impurity profiles. We adhere to current Good Manufacturing Practices (cGMP) where applicable, and our quality protocols are designed to meet the stringent requirements of pharmaceutical R&D and production. Certificates of Analysis are available upon request.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated area at a controlled room temperature (typically 15-25°C). The material should be kept under an inert atmosphere if long-term stability is required. Keep away from heat and incompatible materials.

Specification

Item	Specification
Appearance	White to off-white solid
Identification (IR)	Conforms to structure
Identification (HPLC)	Retention time matches reference standard
Assay (HPLC)	≥98.0%
Related Substances (HPLC)	Total impurities ≤2.0%
Any single unknown impurity	≤0.5%
Residual Solvents (GC)	Complies with ICH Q3C
Water Content (KF)	≤0.5%
Specific Rotation	Contact for details

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