Buy Propafenone Hydrochloride Powder Raw Anti-arrhythmic Medication Online CAS 34183-22-7
Propafenone Hydrochloride Specification
Product Name: Propafenone Hydrochloride
CAS: 34183-22-7
Level: Medical grade
Content: 98%
Appearance: white powder
Packing: 1kg/aluminum foil bag detachable
Physical and chemical properties: white crystalline powder; odorless, bitter, slightly soluble in ethanol, chloroform or glacial acetic acid, very slightly soluble in water;
Category: Pharmaceutical raw materials
Area: Antiarrhythmia
Down products: tablets, injections, capsules
Application: For the prevention and treatment of ventricular or supraventricular ectopic pulsation, tachycardia, pre-excitation syndrome and prevention of ventricular fibrillation after electric shock
Dosage: Oral. 100 to 200 mg (2 to 4 tablets) once a day, 3 to 4 times a day. The amount of treatment, 300 ~ 900mg (6 ~ 18 tablets) a day, 4 ~ 6 times a day. The maintenance dose is 300 to 600 mg (6 to 12 tablets) per day, and is taken in 2 to 4 times. Due to its local anesthetic effect, it should be swallowed after meals or with food, and should not be chewed.
What is Propafenone?
Propafenone brand name Rythmol SR or Rytmonorm is a class 1C anti-arrhythmic medication, which treats illnesses associated with rapid heart beats such as atrial and ventricular arrhythmias
Propafenone Hydrochloride Certificate of Analysis
| Product name |
Propafenone Hydrochloride |
| CAS No. |
34183-22-7 |
Outer Packing |
1kg/foil bag |
| Production date |
2017.11.02 |
Shelf life |
2019.11.01 |
| Standard adopted |
USP36 |
| Items of analysis |
Specification |
Results |
| Appearance |
White powder |
White powder |
| Identification |
B:meets the requirements |
Conform |
| Clarity of solution |
1.0g-30ml hot water, immediately observed, the solution should be clarified |
Conform |
| Dissolution process |
171-175℃ |
172.7-173.5℃ |
| pH |
5.0-6.2 |
5.77 |
| Loss on drying |
Not more than 0.5% |
0.062% |
| Residue on ignition |
Not more than 0.1% |
0.030% |
| Heavy metals |
Not more than 20ppm |
Conform |
| Chromatographic purity |
impurity B≤0.1%,impurity D≤0.1%,impurity |
B:N/D |
| Chromatographic purity |
G≤0.1% impurity C≤0.1%,impurity F≤0.1% |
D:0.046% |
| Single impurity |
≤0.1% |
0.034% |
| Total impurities |
≤0.3% |
0.17% |
| Residual solvent |
Acetone≤0.5% |
N/D |
| Residual solvent |
Ethanol≤0.5% |
0.034% |
| Assay |
According to the dry product, the content of hydrochloric acid is 98.0%-102.0% |
99.96% |
| Conclusion |
Qualified |
