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Sancycline Hydrochloride CAS NO 6625-20-3
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CAS No.:6625-20-3
Grade:Pharmacy Grade
Content:99.9%
Brand:Customizable
Packaging:Customizable
Description
Sancycline Hydrochloride CAS NO 6625-20-3 is a chemically modified tetracycline derivative, primarily valued as a key intermediate in pharmaceutical synthesis. Its significance lies in its role as a precursor for the development of novel semi-synthetic tetracycline antibiotics, which are crucial in addressing antibiotic resistance. This high-purity compound is essential for research institutions and manufacturers in the pharmaceutical and biotechnology sectors focused on antimicrobial drug discovery and development.
Application
- Pharmaceutical Intermediate: A critical building block for the synthesis of next-generation tetracycline-class antibiotics, such as tigecycline analogs.
- Antimicrobial Research: Used in biochemical and microbiological research to study structure-activity relationships (SAR) and mechanisms of action against resistant bacterial strains.
- Reference Standard: Serves as a high-purity analytical reference standard in quality control (QC) and research and development (R&D) laboratories for method development and validation.
- Chemical Synthesis: Employed in organic synthesis for the preparation of novel chemical entities with potential therapeutic applications beyond antibiotics.
Basic Information
| Product Name | Sancycline Hydrochloride |
| CAS No. | 6625-20-3 |
| Molecular Formula | C22H24N2O8 • HCl |
| Molecular Weight | 480.90 g/mol |
| Synonyms | 6-Deoxy-6-demethyltetracycline Hydrochloride; 6-Deoxytetracycline Hydrochloride; Santycin Hydrochloride; 4-(Dimethylamino)-1,4,4a,5,5a,6,11,12a-octahydro-3,6,10,12,12a-pentahydroxy-6-methyl-1,11-dioxo-2-naphthacenecarboxamide Hydrochloride; 6-Desmethyl-6-deoxytetracycline HCl; Antibiotic U-24729A |
| EINECS | Contact for details |
Quality Control
Our Sancycline Hydrochloride is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing, including HPLC for purity, identification by IR and NMR spectroscopy, and tests for residual solvents and heavy metals, to ensure it meets stringent standards for pharmaceutical intermediates. A detailed Certificate of Analysis (COA) is provided with every shipment to guarantee traceability and compliance with your specifications.
Storage
Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated area at a controlled room temperature (15-25°C). Due to its hygroscopic (moisture-sensitive) nature, the container must be kept tightly sealed after each use to prevent degradation from atmospheric moisture.
Specification
| Item | Specification |
|---|---|
| Appearance | Yellow to light yellow powder |
| Identification (IR) | Conforms to reference spectrum |
| Identification (HPLC) | Retention time corresponds to reference standard |
| Assay (HPLC) | ≥ 98.0% |
| Water Content (KF) | ≤ 2.0% |
| Residue on Ignition | ≤ 0.5% |
| Heavy Metals | ≤ 20 ppm |
| Related Substances (HPLC) | Total impurities ≤ 2.0% |
Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.
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