| Function: | Antibiotic and Antimicrobial Agents |
|---|---|
| Certification: | GMP |
| Grade Standard: | Medicine Grade |
| Type: | Analysis reagent |
| State: | Solid |
| Volatile: | Not Volatile |
| Samples: |
|---|
| Customization: |
|---|
Suppliers with verified business licenses
Audited Supplier Quick Details:
| Product name | Ranitidine Hydrochloride |
| CAS NO. | 66357-59-3 |
| Synonyms | Ranitidine Hydrochloride |
| Category | Pharmaceutical Raw Materials,Active Pharmaceutical Ingredients,Bulk Drugs,Fine Chemicals. |
| Purity | 99% Ranitidine Hydrochloride |
| Appearance | Ranitidine Hydrochloride powder |
| Shelf life | 2 years for Ranitidine Hydrochloride |
| Product Name | Ranitidine Hcl |
| Package | 25KG Drum |
| Description | White to pale yellow, crystalline practically odorless powder |
| Identification | A.The IR absorption spectrum of the test specimen comply with that of the corresponding USP Reference Standard B.Absorptivities at 229nm and 315nm ,do not differ by more than 3.0% C. A solution of it meets the requirements of Chloride. |
| pH | Should be 4.5~6.0 |
| Loss on drying | ≤0.75% |
| Residue on ignition | ≤0.1% |
| Chromatographic purity | Ranitidine related Compound B: ≤0.5% Any other impurity: ≤0.3% The sum of all impurities: ≤1.0% |
| Organic volatile impurities | Meet the requirements |
| Residual solvents | Alcohol: ≤0.5% |
| Assay | Assay (Dried basis C13H22N4O3S·HCl 97.5%~102%) |
Suppliers with verified business licenses
Audited Supplier 
){kind=link}
){kind=link}