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(R)-(-)-Citalopram CAS NO 128196-02-1
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CAS No.:128196-02-1
Grade:Pharmacy Grade
Content:99.9%
Brand:Customizable
Packaging:Customizable
Description
(R)-(-)-Citalopram CAS NO 128196-02-1 is the single enantiomer of the widely used selective serotonin reuptake inhibitor (SSRI), Citalopram. This high-purity chiral intermediate is critical for pharmaceutical research and development focused on enantiomerically pure active pharmaceutical ingredients (APIs). It is primarily utilized by pharmaceutical manufacturers and advanced research institutions engaged in the synthesis of novel therapeutics, process optimization, and stereochemical studies related to neuropharmacology.
Application
- Pharmaceutical Intermediate: Key chiral building block for the synthesis of enantiomerically pure (R)-Citalopram and related derivative APIs.
- Research & Development: Essential reference standard and starting material for pharmacological research, metabolic studies, and analytical method development.
- Process Chemistry: Used in route scouting and optimization for the commercial-scale production of the (R)-enantiomer.
- Analytical Standard: Serves as a high-purity certified reference material (CRM) for HPLC, LC-MS, and chiral analysis to ensure quality control.
- Asymmetric Synthesis Studies: Valuable substrate for developing and testing new chiral catalysts and synthetic methodologies.
Basic Information
| Product Name | (R)-(-)-Citalopram |
| CAS No. | 128196-02-1 |
| Molecular Formula | C20H21FN2O |
| Molecular Weight | 324.39 g/mol |
| Synonyms | (R)-Citalopram; (R)-1-[3-(Dimethylamino)propyl]-1-(4-fluorophenyl)-1,3-dihydroisobenzofuran-5-carbonitrile; (R)-1-(3-Dimethylaminopropyl)-1-(4-fluorophenyl)-5-phthalancarbonitrile; Escitalopram Impurity; (R)-Lu 10-005-B; UNII-0K47S5P26T |
| EINECS | Contact for details |
Quality Control
Our (R)-(-)-Citalopram is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing, including chiral purity determination by HPLC, to ensure it meets stringent specifications for pharmaceutical R&D use. A detailed Certificate of Analysis (COA) providing batch-specific results for identity, purity, and impurities is supplied with every order.
Storage
Preserve in a tightly closed container, protected from light. Store in a cool, dry place at controlled room temperature (15-25°C). The product is light-sensitive and should be handled under appropriate conditions to maintain stability.
Specification
| Item | Specification |
|---|---|
| Appearance | White to off-white powder |
| Identification (IR) | Conforms to structure |
| Identification (HPLC) | Retention time matches reference standard |
| Assay (HPLC) | ≥98.0% |
| Chiral Purity (HPLC) | ≥99.0% (R)-enantiomer |
| Related Substances (HPLC) | Total impurities ≤2.0% |
| Residual Solvents (GC) | Complies with ICH Q3C guidelines |
| Loss on Drying | ≤0.5% |
Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.
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