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Omiloxetine CAS NO 176894-09-0
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CAS No.:176894-09-0
Grade:Pharmacy Grade
Content:99.9%
Brand:Customizable
Packaging:Customizable
Description
Omiloxetine CAS NO 176894-09-0 is a high-purity pharmaceutical intermediate and research chemical. This compound is of significant interest for its role in the development and synthesis of novel therapeutic agents. It is primarily utilized by pharmaceutical R&D laboratories, contract manufacturing organizations (CMOs), and academic research institutions engaged in medicinal chemistry and process development.
Application
- Pharmaceutical Intermediate: A key building block in the synthesis of active pharmaceutical ingredients (APIs) and novel drug candidates.
- Medicinal Chemistry Research: Used in structure-activity relationship (SAR) studies and lead optimization programs within R&D settings.
- Process Development & Scale-up: Serves as a critical raw material for developing and optimizing scalable synthetic routes in pilot plants and commercial manufacturing.
- Reference Standard: Can be utilized as an analytical standard for method development, validation, and quality control testing in pharmaceutical analysis.
- Biochemical Research: Employed in biochemical assays and pharmacological studies to investigate specific biological pathways and mechanisms of action.
Basic Information
| Product Name | Omiloxetine |
| CAS No. | 176894-09-0 |
| Molecular Formula | C17H19NO2 |
| Molecular Weight | 269.34 g/mol |
| Synonyms | Omiloxetine; (3S)-3-(Methylamino)-1-(2-naphthyl)propan-1-ol; LY-248686; Tomoxetine Impurity; (S)-Tomoxetine; N-Methyl(S)-Norphenylephrine; (S)-3-(Methylamino)-1-(naphthalen-2-yl)propan-1-ol |
| EINECS | Contact for details |
Quality Control
Our Omiloxetine is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing to ensure identity, purity, and consistency. We provide Certificates of Analysis (COA) detailing specifications such as assay, chiral purity, and impurity profiles. Our quality commitment aligns with cGMP principles for pharmaceutical intermediates, ensuring reliable supply for critical development and manufacturing processes.
Storage
Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated area at 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 |
| Identification (HPLC) | Conforms |
| Assay (HPLC) | ≥ 98.0% |
| Chiral Purity (Chiral HPLC) | ≥ 99.0% |
| Related Substances (HPLC) | Individual impurity ≤ 0.5% Total impurities ≤ 1.5% |
| Residual Solvents (GC) | Complies with ICH Q3C |
| Loss on Drying | ≤ 1.0% |
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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Our in-house lab drives process innovation, new product development, and tailored synthesis solutions.






