100.1% Pharmaceutical Raw powder Enalapril maleate to treat high blood pressure
100.1% Pharmaceutical Raw powder Enalapril maleate to treat high blood pressure
| Purchase Qty | Unit | Fob Price |
|---|---|---|
| ≥10 | g(s) | Negotiable |
Payment Terms: T/T,,Money Gram,Others
Get Latest PriceActive Ingredients:
Chemical Formula: C24H32N2O9
Molecular Weight: 492.52
Assay: 99.65%
Pharmacopeia: CP
Package Type: As your request
Shelf Life: 18 months
Storage: Sealed
Place of Origin: Wuhan,Hubei
Appearance: white powder
Molecular Formula: C24H32N2O9
Enalapril maleate
Molecular Formula:C24H32N2O9
Formula Weight:492.52
CAS No.:76095-16-4
Appearance:white powder
Purity:100.1%
Standard:USP standard
Enalapril maleate is part of a class of drugs called angiotensin-converting which prevents the constriction of blood vessels.Enalapril maleate is used to treat high blood pressure, congestive heart failure, and left ventricular dysfunction. As an ACE inhibitor, it works by blocking the angiotensin-converting enzyme, causing blood vessels to relax, which can lower blood pressure. The tablets are generally taken once or twice daily. Side effects may include cough, low blood pressure, and dizziness.
The COA of Enalapril maleate:
| Product name | Enalapril maleate | |||
| CAS No. | 76095-16-4 | Outer Packing | 25kg drum | |
| Production date | 20151024 | Shelf life | ||
| Standard adopted | USP | |||
| Items of analysis | Specification | Results | ||
| Appearance | A white or almost white crystalline powder | Almost white crystalline powder | ||
| Solubility | Freely soluble in methanol, sparingly soluble in water, practically insoluble in dichloromethane | Conforms | ||
| Identification | The infrared absorption spectrum is concordant with Enalapril Maleate RS. | Conforms | ||
| Identification | The retention time of the major peak in the chromatogram of Test solution corresponds to that in the chromatogram of the Standard solution, as obtained in the Assay. | Conforms | ||
| Melting range | About 144 ℃ | 143~144 ℃ | ||
| Specific rotation | -41.0°~ -43.5° | -41.7° | ||
| Loss on drying | Not more than 1.0% | 0.10% | ||
| Residue on ignition | Not more than 0.2% | 0.10% | ||
| Heavy metals | Not more than 0.001% | ＜0.001% | ||
| Residual solvents(GC) Ethanol | Not more than 0.5% | ＜LOD | ||
| Impurity(RRT=1.10) | Not more than 1.0% | N.D | ||
| Any other individual impurity | Not more than 0.3% | 0.19% | ||
| Total impurities | Not more than 1.0% | 0.33% | ||
| Assay | 98.0%~102.0% | 100.10% | ||
| Conclusion | Qualified | |||
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