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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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