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Cetirizine Descarboxymethyl R-Isomer CAS NO 705289-61-8
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CAS No.:705289-61-8
Grade:Pharmacy Grade
Content:99.9%
Brand:Customizable
Packaging:Customizable
Description
Cetirizine Descarboxymethyl R-Isomer is a key chiral intermediate in the synthesis of advanced pharmaceutical compounds. This high-purity isomer is critical for ensuring the enantiomeric purity and efficacy of the final active pharmaceutical ingredient (API). It is primarily required by pharmaceutical R&D laboratories and manufacturers engaged in the production of enantiomerically pure antihistamines and related therapeutic agents.
Application
- Pharmaceutical Intermediate: A critical building block in the synthesis of enantiomerically pure Cetirizine and its derivatives.
- Active Pharmaceutical Ingredient (API) Development: Used in research and process development for new chiral drug candidates.
- Reference Standard: Serves as a high-purity standard for analytical method development and quality control in pharmaceutical analysis.
- Process Chemistry: Employed in route scouting and optimization for the commercial-scale manufacturing of chiral pharmaceuticals.
- Asymmetric Synthesis Research: A valuable compound for academic and industrial research in stereoselective synthesis methodologies.
Basic Information
| Product Name | Cetirizine Descarboxymethyl R-Isomer |
| CAS No. | 705289-61-8 |
| Molecular Formula | C19H22ClN3O2 |
| Molecular Weight | 359.85 g/mol |
| Synonyms | (R)-2-(2-(4-((4-Chlorophenyl)(phenyl)methyl)piperazin-1-yl)ethoxy)ethanol; (R)-Cetirizine Descarboxymethyl; R-Cetirizine Descarboxymethyl; Levocetirizine Descarboxymethyl Intermediate; (R)-2-[2-[4-[(4-Chlorophenyl)phenylmethyl]-1-piperazinyl]ethoxy]ethanol; ZYRTEC Descarboxymethyl R-Isomer |
| EINECS | Contact for details |
Quality Control
Our Cetirizine Descarboxymethyl R-Isomer is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing, including chiral purity assay and impurity profiling by HPLC, to ensure it meets the stringent requirements for pharmaceutical intermediates. Certificates of Analysis (COA) documenting identity, purity, and chiral excess are provided with every shipment.
Storage
Preserve in a tightly closed container, protected from light. Store in a cool, dry place at controlled room temperature (15-25°C). The material is hygroscopic; keep the container tightly sealed in a dry environment to prevent moisture absorption.
Specification
| Item | Specification |
|---|---|
| Appearance | White to off-white powder |
| Identification (IR) | Conforms to structure |
| Identification (HPLC) | Conforms to reference |
| Assay (HPLC) | ≥ 98.0% |
| Chiral Purity (Chiral HPLC) | ≥ 99.0% |
| Related Substances (HPLC) | Total impurities ≤ 2.0% Any single impurity ≤ 1.0% |
| Residual Solvents (GC) | Meets ICH Q3C guidelines |
| 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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