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Levormeloxifene CAS NO 78994-23-7
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CAS No.:78994-23-7
Grade:Pharmacy Grade
Content:99.9%
Brand:Customizable
Packaging:Customizable
Description
Levormeloxifene is a selective estrogen receptor modulator (SERM) of significant pharmaceutical interest. This compound is valued for its targeted biological activity and serves as a key intermediate or active pharmaceutical ingredient (API) in advanced research and development. It is primarily utilized by pharmaceutical companies, biotechnology research institutions, and contract development and manufacturing organizations (CDMOs) engaged in the development of novel therapeutics. Our supply of Levormeloxifene CAS NO 78994-23-7 is characterized by stringent quality control to ensure reliability for critical applications.
Application
- Pharmaceutical Intermediate: Serves as a critical building block in the synthesis of advanced therapeutic agents targeting estrogen-related pathways.
- Research & Development: Used in preclinical and clinical research to study the effects of selective estrogen receptor modulation.
- Reference Standard: Employed as a high-purity analytical standard for quality control and method validation in pharmaceutical analysis.
- Biochemical Research: Utilized in vitro and in vivo studies to investigate receptor binding affinity, pharmacokinetics, and metabolic profiles.
- API Manufacturing: Incorporated into the production of finished dosage forms under controlled Good Manufacturing Practice (GMP) environments.
Basic Information
| Product Name | Levormeloxifene |
| CAS No. | 78994-23-7 |
| Molecular Formula | C29H35NO4 |
| Molecular Weight | 461.60 g/mol |
| Synonyms | (-)-Levormeloxifene; (3S)-3-(4-Methoxyphenyl)-4-methyl-2-{4-[2-(1-pyrrolidinyl)ethoxy]phenyl}-2H-1-benzopyran-7-ol; FC-1271a; Levormeloxifene Hydrochloride (salt form); Centchroman isomer; Ormeloxifene enantiomer |
| EINECS | Contact for details |
Quality Control
Our Levormeloxifene is manufactured and tested under a rigorous quality management system. Each batch is analyzed to meet high-purity standards suitable for pharmaceutical research and development. Comprehensive testing includes identity confirmation, assay, and impurity profiling via advanced analytical techniques. A Certificate of Analysis (COA) detailing all specifications and results is provided with every shipment to ensure full traceability and compliance.
Storage
Preserve in a tightly closed container, protected from light. Store in a cool, dry place at a controlled room temperature (15-25°C). This material is hygroscopic (moisture-sensitive) and must be kept under anhydrous conditions. For long-term storage, consider storing under an inert atmosphere.
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% |
| Single Maximum Unknown 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.
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Each batch undergoes strict QC, accompanied by COA, MSDS, and full compliance with international standards.
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