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Valsartan 137862-53-4

98% up by HPLC, EP/USP/JP

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Product Detail

Product Information

Product name	Valsartan
CAS No.	137862-53-4
Molecular Formula	C24H29N5O3
Molecular Weight	435.519
Quality Standard	98% up, USP/JP/EP
Appearance	White to almost white powder

COA of Valsartan

ITEMS	STANDARDS	RESULTS
Appearance	White to almost white powder	White powder
Identification	Infrared absorption: The IR spectrum is consistent with that obtained with the reference	Conforms
Identification	The retention time of the major peak in the chromatogram of the assay preparation corresponds to that in the chromatogram of the standard preparation, as obtained in the assay	Conforms
Absorbance	NMT 0.02	0.003
Water	NMT2.0%	0.56%
Residue on ignition	NMT0.1%	0.06%
Heavy metals	NMT0.001%
Related compounds (HPLC)	Compound A NMT1.0%	0.49%
	Compound B NMT0.2%	0.08%
	Compound C NMT0.1%	Undetected
	Any other individual impurity NMT0.1% (excluding compound A )	0.04%
	Total impurities NMT0.3% (excluding compound A )	0.20%
Residual solvents(GC)	Ethyl acetate NMT5000ppm	2820ppm
	Dichloromethane NMT600ppm	Undetected
	Methanol NMT3000ppm	Undetected
	N,N-Dimethylformamide NMT880ppm	Undetected
Assay	98.0—102.0%	99.2%
Conclusion	The analysis results show that this batch of valsartan conforms to USP

Usage

Function of Valsartan

Valsartan is an angiotensin II receptor antagonist anti-hypertensive drug. The drug can block the type I (AT1) receptor of angiotensin II, increase the plasma level of angiotensin II and stimulate The unblocked AT2 receptor also counteracts the role of the AT1 receptor, so as to achieve the effect of dilating blood vessels and lowering blood pressure, the effect is lasting and stable, and the toxic and side effects are small. Therefore, valsartan is mainly suitable for antihypertensive, mild to moderate primary hypertension, especially for the treatment of secondary hypertension caused by kidney damage.