Purity: | USP37 |
---|---|
Model Number: | 137862-53-4 |
Brand Name: | Tianrui |
Grade Standard: | Medicine Grade |
Type: | Anti-hypertensive /Anti-hyperlipidemic |
Place of Origin: | China (Mainland) |
MF: | C24H29N5O3 |
CAS No.: | 137862-53-4 |
Packaging: 25K g/drum: | Characteristics:white or white crystalline powder |
Quick Details
Specifications
CAS 137862-53-4 Anti Hypertensive Medication Valsartan Medication
Quick Details:
Chemical Name: Valsartan
Molecular Formula: C24H29N5O3
Formula Weight: 435.5188
CAS NO.: 137862-53-4
Purity: 99%
Characteristics:white or white crystalline
Powder
Quality standard: USP
Packaging: 25K g/drum
Usage:it's used for various types of
Hypertension,and has the better protection effect on cardiovascular and renal.
It can be routinely used by Hypertensive patients who are Myocardial
Infarction, heart failure, proteinuria, diabetes. It's also can be combined
with diuretics (such as hydrochlorothiazide)
Description:
Valsartan is an angiotensin-receptor Blocker that may be used to treat a variety of cardiac conditions including Hypertension, diabetic nephropathy and heart failure. Valsartan lowers blood Pressure by antagonizing the renin-angiotensin-aldosterone system; it competes with angiotensin II for binding to the type-1 angiotensin II receptor subtype and prevents the blood pressure increasing effects of angiotensin II.
Specification:
Test Items |
Standard |
Result | ||
Description |
White or off-white powder,odorless,slightly hygroscopy Hygroscopy |
Qualified | ||
Solubility |
Free soluble in methanol and Ethanol,sparingly soluble in ethyl acetate,slightly soluble in Dichloromethane, particularly insoluble in water |
Qualified | ||
Identification |
IR,HPLC Must conform to reference standard |
Qualified | ||
Absorbance at 420nm |
≤0.02 |
<0.01 | ||
Water(KF) |
≤2.0% |
0.4% | ||
Residue on Ignition |
≤0.1% |
<0.1% | ||
Heavy Metals |
≤10ppm |
<10ppm | ||
Related compounds | ||||
D-valsartan | ≤1.0% |
0.49% | ||
Butyryl-valsartan | ≤0.2% |
0.02% | ||
Benzyl-valsartan | ≤0.1% |
N.D. | ||
Any Other individual impurity | ≤0.1% |
0.03% | ||
Total Impurities(ExcludingD-valsartan) | ≤0.3% |
0.11% | ||
Residual Solvents | ||||
Ethanol | NMT5000ppm |
N.D | ||
Ethyl acetate | NMT5000ppm |
2283ppm | ||
Toluene | NMT890ppm |
89ppm | ||
Assay(HPLC) |
98.0%-102.0% |
100.3% | ||
Conclusion |
the results conform with USP37 | |||
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