Azithromycin EP Impurity E, PurCert
PurCert
Properties
| Assay Purity | >=92 % |
| M pt. | NA |
| Form | Solid |
Safety Information
| Hazard Statement(s) | NA |
| Precautionary Statement | NA |
| GHS Pictogram | |
| Signal word | NA |
| HS Code | NA |
| Storage Temp. | 2-8°C |
| Storage Class | 11 - Combustible Solids |
| UN Number | NA |
Description
Application
Pharmaceutical analysis- identification and quantification of impurity E in azithromycin. Quality control- used in HPLCUPLC method development and validation. Stability testing- monitoring degradation pathways of the drug.
Purpose
To ensure impurity levels comply with EP limits. Support regulatory and quality assurance requirements. Confirm the purity safety and consistency of azithromycin products.
General Description
It is typically a process-related or degradation impurity formed during the manufacture or storage of azithromycin. It is supplied as a high-purity reference standard for analytical use.
Documents
| SDS | |
| COA | |
| Specification | |
| Bulk quote order form | |
| Sample COA |