Powder: | Yes |
---|---|
Customized: | Non-Customized |
Certification: | GMP, ISO 9001 |
Suitable for: | Adult |
State: | Solid |
Purity: | >99% |
Samples: |
---|
Suppliers with verified business licenses
Product Description
English name: Valsartan
Anothername:3-methyl-2-[pentanoyl-[[4-[2-(2h-tetrazol-5-yl)phenyl]phenyl]methyl]amino]-butanoic acid
Synonyms:L-Valine,N-(1-oxopentyl)-N-[[2'-(1H-tetrazol- 5-yl)[1,1'-biphenyl]-4-yl]methyl]-;Diovan;Diovan (TN);L-Valine, N-(1-oxopentyl)-N-((2-(1H-tetrazol-5-yl)(1,1-biphenyl)-4-yl)methyl)-;N-(p-(o-1H-Tetrazol-5-ylphenyl)benzyl)-N-valeryl-L-valine;Valsartan [USAN:INN];N-(1-n.Pentanoyl)-N-[[2'-(1H-tetrazol-5-yl)[1',1- biphenyl]-4-yl]methyl]-L-valine;Dihydrotachystero;Valsartan USP30
Specification: 98%
CAS NO.: 137862-53-4
Standards:EP, USP
Appearance: white crystalline powder
Molecular weight:435.5188
Molecular formula:C24H29N5O3
Boilling point: 684.9°C at 760 mmHg
Certification of Analysis
ITEMS |
SPECIFICATION |
Appearance |
White or off white powder |
Solubility |
Very soluble in methanol and ethanol.sparingly soluble in chloroform practically insoluble in water |
Identification |
|
--IR |
Similar to standard |
--HPLC |
Similar to standard |
Absorbance |
NMT0.02 at 420nm(1/20 in methanol ) |
Water |
NMT 2.00% |
Residue on ignition |
NMT 0.1% |
Heavy metals |
NMT 0.001% |
Related compounds Related compounds A Related compounds B Related compounds C Any other individual impurity Total impurities(not include related compound A ) |
NMT1.0% NMT0.2% NMT0.1% NMT0.1% NMT0.3% |
Assay (HPLC) |
NLT98.0% and NMT102.0% Calculated on the anhydrous basis |
Suppliers with verified business licenses