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L-Glutamic Acid, Compound With Erythromycin (1:1) CAS NO 16667-03-1
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CAS No.:16667-03-1
Grade:Pharmacy Grade
Content:99.9%
Brand:Customizable
Packaging:Customizable
Description
L-Glutamic Acid, Compound With Erythromycin (1:1) is a pharmaceutical salt formed by the combination of the amino acid L-glutamic acid and the macrolide antibiotic erythromycin. This specific 1:1 molecular complex is engineered to enhance the stability, solubility, or bioavailability profile of the active pharmaceutical ingredient. It is a critical intermediate or active component primarily for the development and manufacturing of specialized antibiotic formulations. Target industries include pharmaceutical synthesis, veterinary medicine, and advanced research into antimicrobial agents.
Application
- Pharmaceutical Intermediate: Serves as a key starting material or active component in the synthesis of advanced antibiotic drugs.
- Veterinary Pharmaceuticals: Used in formulating treatments for bacterial infections in livestock and companion animals.
- Antimicrobial Research: Employed in R&D for studying modified erythromycin derivatives with improved pharmacological properties.
- Drug Delivery Systems: Utilized in developing formulations aimed at enhancing drug stability and controlled release.
- Reference Standard: Acts as a certified reference material for quality control and analytical testing in regulatory compliance.
Basic Information
| Product Name | L-Glutamic Acid, Compound With Erythromycin (1:1) |
| CAS No. | 16667-03-1 |
| Molecular Formula | C37H67NO13 • C5H9NO4 |
| Molecular Weight | Contact for details |
| Synonyms | Erythromycin L-glutamate; Erythromycin glutamate salt; Erythromycin compound with L-glutamic acid (1:1); L-Glutamic acid erythromycin salt; Glutamic acid, L-, compd. with erythromycin (1:1); Erythromycin glutamic acid complex; AB-Fortisin (trade name variant); Erythromycinium glutamate |
| EINECS | Contact for details |
Quality Control
Our L-Glutamic Acid, Compound With Erythromycin (1:1) is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing, including identification, assay, and impurity profiling, to ensure it meets high-purity standards suitable for pharmaceutical applications. A Certificate of Analysis (COA) detailing specific results for purity, related substances, and residual solvents 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 opening to prevent degradation from atmospheric moisture. Keep away from incompatible materials.
Specification
| Item | Specification |
|---|---|
| Appearance | White to off-white powder |
| Identification (IR) | Conforms to standard |
| Assay (HPLC) | ≥ 98.0% |
| Water Content (KF) | ≤ 2.0% |
| Related Substances (HPLC) | Total impurities ≤ 2.0% |
| Residual Solvents (GC) | Complies with ICH guidelines |
| Specific Rotation | Contact for details |
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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