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Zalcitabine Monophosphate Ammonium Salt CAS NO 1179343-05-5
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CAS No.:1179343-05-5
Grade:Pharmacy Grade
Content:99.9%
Brand:Customizable
Packaging:Customizable
Description
Zalcitabine Monophosphate Ammonium Salt is a key nucleotide analog intermediate with significant pharmaceutical relevance. This compound is primarily valued for its role in the synthesis of active pharmaceutical ingredients (APIs) for antiviral therapies. It is essential for research institutions and manufacturers engaged in the development and production of nucleoside-based antiviral drugs, particularly for targeting retroviruses.
Application
- Active Pharmaceutical Ingredient (API) Intermediate: Critical precursor in the synthesis of Zalcitabine and related nucleoside analog drugs.
- Antiviral Drug Research & Development: Used as a building block in medicinal chemistry for creating new therapeutic candidates against viral infections.
- Biochemical Research: Serves as a substrate or standard in enzymatic studies and metabolic pathway investigations.
- Pharmaceutical Manufacturing: Employed in scaled-up GMP production processes for finished dosage forms.
- Reference Standard: Utilized as a high-purity certified reference material (CRM) for quality control and analytical method development.
Basic Information
| Item | Detail |
|---|---|
| Product Name | Zalcitabine Monophosphate Ammonium Salt |
| CAS No. | 1179343-05-5 |
| Molecular Formula | C9H16N4O7P |
| Molecular Weight | 323.22 g/mol |
| Synonyms | 2',3'-Dideoxycytidine monophosphate ammonium salt; ddCMP ammonium salt; Zalcitabine 5'-monophosphate ammonium salt; 4-Amino-1-((2R,5S)-5-(hydroxymethyl)tetrahydrofuran-2-yl)-2(1H)-pyrimidinone 5'-(dihydrogen phosphate) ammonium salt; Ammonium zalcitabine monophosphate |
| EINECS | Contact for details |
Quality Control
Our Zalcitabine Monophosphate Ammonium Salt is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing, including HPLC for purity, NMR and IR for structural confirmation, and stringent controls for residual solvents and impurities. Certificates of Analysis (COA) are provided, detailing compliance with in-house specifications developed for pharmaceutical intermediate applications.
Storage
Preserve in a tightly closed container, protected from light. Store in a cool, dry place at a controlled room temperature (15-25°C). Due to its hygroscopic nature, the container must be kept sealed in a dry environment to prevent moisture absorption. For long-term storage, consider desiccants or inert atmosphere.
Specification
| Item | Specification |
|---|---|
| Appearance | White to off-white powder |
| Identification (HPLC) | Conforms to reference standard |
| Identification (IR) | Conforms to structure |
| Assay (HPLC) | ≥ 98.0% |
| Water Content (KF) | ≤ 2.0% |
| Residual Solvents (GC) | Meets ICH guidelines |
| Heavy Metals | ≤ 20 ppm |
| Bacterial Endotoxins | < 0.5 EU/mg (if applicable) |
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.






