Powder: | Yes |
---|---|
Customized: | Non-Customized |
Certification: | GMP, HSE, ISO 9001, USP, BP |
State: | Powder |
Purity: | >99% |
CAS: | 76095-16-4 |
Samples: |
---|
Customization: |
---|
Suppliers with verified business licenses
Produet Name | Enalapril maleate | |||||
Batch No | 5112-20-001 | Batch Size | 622.72kg | |||
Batch Type | Commercial | Report Date | 2020-01-09 | |||
Retest Date | 2023-12-31 | Storage Condition | Preserved in a well-closed container | |||
Manufactrue Date | 2020-01-01 | Manufactrue Site | Xunqiao,Linhai,Zhejiang,317024,China | |||
Reference | USP | |||||
Test | Specification | Results | ||||
Appearance | White or almost white crystalline powder | Almost white crystalline powder |
||||
Solubility | Frecly soluble in methanol, sparingly soluble in water, practically insoluble in dichloromethane |
Conforms | ||||
Melting Point | About 144ºC | 143-144ºC | ||||
Specific rotation | -41.0°~43.5° | -41.8° | ||||
Identification | I)The infrared absorption spectrum is concordant with Enalapril Maleate RS. |
Conforms | ||||
Identification | 2)The retention time of the major peak of the Sample solution corresponds to that of the Standard solution,as obtained in the Assay. |
Conforms | ||||
Loss on drying | ≤1.0% | <0.1% | ||||
Residue on ignition | ≤0.2% | <0.1% | ||||
Related substances Impurity (RRT=1.10) |
≤1.0% | N.D | ||||
Related substances Total impurities |
≤1.0% | 0.33% | ||||
Related substances Any other impurity |
≤0.3% | 0.14% | ||||
Residual solvents(GC) Ethanol |
≤5000ppm | N.D | ||||
Assay(HPLC) | 98.0~102.0%(Calculated on the dried basis) | 99.4% | ||||
Conclusion | Complies with USP |
mode of transportation | ||
By Air | By Express | By Sea |
suitable for >50 | suitable for sampple order or <50 | suitable for >300 |
Fast:3-7 days | Fast:3-10 days | Fast: 7-45 days |
lower than the express cost | high shipping cost | lowest cost |
Suppliers with verified business licenses