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Dextrofemine CAS NO 15687-08-8
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CAS No.:15687-08-8
Grade:Pharmacy Grade
Content:99.9%
Brand:Customizable
Packaging:Customizable
Description
Dextrofemine CAS NO 15687-08-8 is a specialized chiral compound of significant interest in advanced pharmaceutical research and development. Its primary value lies in its stereochemical purity, which is critical for producing enantiomerically specific therapeutic agents with targeted biological activity. This high-purity intermediate is essential for manufacturers in the pharmaceutical and fine chemical sectors focused on developing novel central nervous system (CNS) drugs, chiral catalysts, and other high-value synthetic applications.
Application
- Key chiral intermediate in the synthesis of advanced pharmaceutical active ingredients (APIs).
- Research and development of novel therapeutics targeting the central nervous system.
- Building block for the preparation of enantiomerically pure compounds in fine chemical synthesis.
- Potential use in the development of chiral ligands and catalysts for asymmetric synthesis.
- Reference standard for analytical method development and quality control in pharmaceutical manufacturing.
- Starting material for investigational new drugs (INDs) in preclinical and clinical studies.
Basic Information
| Product Name | Dextrofemine |
| CAS No. | 15687-08-8 |
| Molecular Formula | Contact for details |
| Molecular Weight | Contact for details |
| Synonyms | Dextroamphetamine Impurity; (R)-Femine; Dextro-femine; (R)-1-Phenylpropan-2-amine derivative; Dextroamphetamine related compound; Enantiomer of Levofemine; CAS 15687-08-8 |
| EINECS | Contact for details |
Quality Control
Our Dextrofemine is produced under strict quality management systems to ensure batch-to-batch consistency and high enantiomeric purity. Each lot undergoes comprehensive analytical testing, including chiral HPLC for enantiomeric excess (ee) determination, identity confirmation via spectroscopic methods (IR, NMR), and purity assessment. A detailed Certificate of Analysis (COA) is provided with every shipment, documenting compliance with agreed specifications. We support cGMP standards for pharmaceutical intermediates.
Storage
Preserve in a tightly closed container, protected from light. Store in a cool, dry, well-ventilated area at controlled room temperature (15-25°C). Keep the container tightly sealed to protect from moisture and atmospheric contamination.
Specification
| Item | Specification |
|---|---|
| Appearance | White to off-white solid |
| Identification (IR) | Conforms to reference spectrum |
| Purity (HPLC) | ≥ 98.0% |
| Enantiomeric Purity (Chiral HPLC) | ≥ 99.0% ee |
| Loss on Drying | ≤ 0.5% |
| Residue on Ignition | ≤ 0.1% |
| Heavy Metals | ≤ 10 ppm |
Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.
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Trusted Manufacturer
With our own production facilities, we ensure consistent quality, reliable supply, and full traceability.
Rigorous Quality Assurance
Each batch undergoes strict QC, accompanied by COA, MSDS, and full compliance with international standards.
Advanced R&D Expertise
Our in-house lab drives process innovation, new product development, and tailored synthesis solutions.





