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Erythromycin A 11,12-Carbonate L-Aspartate CAS NO 55171-82-9
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CAS No.:55171-82-9
Grade:Pharmacy Grade
Content:99.9%
Brand:Customizable
Packaging:Customizable
Description
Erythromycin A 11,12-Carbonate L-Aspartate is a chemically modified derivative of the macrolide antibiotic erythromycin, designed to enhance stability and alter pharmacokinetic properties. This compound is critical for pharmaceutical R&D, particularly in the development of novel antibiotic formulations and prodrug strategies to improve bioavailability and patient compliance. It serves as a key intermediate for researchers and manufacturers in the pharmaceutical and fine chemical sectors focused on advanced anti-infective therapies.
Application
- Pharmaceutical Intermediate: Primary use as a key building block in the synthesis of advanced erythromycin derivatives and prodrugs.
- Antibiotic Research & Development: Serves as a critical material for studying structure-activity relationships (SAR) to develop new macrolide antibiotics with improved efficacy.
- Prodrug Synthesis: Utilized in the creation of prodrug formulations aimed at enhancing oral absorption, masking taste, or providing targeted release.
- Reference Standard: Used as a high-purity analytical standard in quality control (QC) and research laboratories for method development and validation.
- Fine Chemical Synthesis: Acts as a specialized intermediate in custom synthesis and contract manufacturing for niche pharmaceutical applications.
Basic Information
| Product Name | Erythromycin A 11,12-Carbonate L-Aspartate |
| CAS No. | 55171-82-9 |
| Molecular Formula | C40H68N2O16 |
| Molecular Weight | 832.98 g/mol |
| Synonyms | Erythromycin A cyclic 11,12-carbonate with L-aspartate; Erythromycin 11,12-carbonate aspartate; L-Aspartic acid, compd. with erythromycin A 11,12-cyclic carbonate (1:1); Erythromycin A cyclic carbonate L-aspartate salt |
| EINECS | Contact for details |
Quality Control
Our Erythromycin A 11,12-Carbonate L-Aspartate is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing, including HPLC for purity and identity confirmation, to ensure it meets exacting standards for pharmaceutical research. A Certificate of Analysis (COA) detailing all test results is provided with every shipment to guarantee traceability and batch-to-batch consistency.
Storage
Preserve in a tightly closed container, protected from light. Store in a cool, dry place at a controlled room temperature (15-25°C). This product is hygroscopic (moisture-sensitive) and must be kept in a dry environment to maintain stability and purity.
Specification
| Item | Specification |
|---|---|
| Appearance | White to off-white powder |
| Identification (IR) | Conforms to reference spectrum |
| Identification (HPLC) | Retention time matches reference standard |
| Assay (HPLC) | ≥ 98.0% |
| Water Content (KF) | ≤ 2.0% |
| Residue on Ignition | ≤ 0.5% |
| Heavy Metals | ≤ 20 ppm |
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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