Valsartan impurity E is a chemical compound used as a pharmaceutical reference standard for analytical testing. It is structurally related to the active pharmaceutical ingredient valsartan and is employed in quality control to ensure the purity and consistency of valsartan drug substances.
콘텐츠 범위: 이 페이지의 정보는 화학물질 식별 및 산업 공급·연구개발·제조 맥락을 대상으로 합니다. 치료 효능 주장, 의료 조언 또는 의약품 사용 지침에 해당하지 않습니다.
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CAS 137863-17-3
Valsartan benzyl ester
pharmaceutical impurity reference standard
발사르탄
active pharmaceutical ingredient
D-Valsartan
pharmaceutical impurity reference standard
Despentanoyl butanoyl valsartan
valsartan impurity reference standard
(2S)-3-methyl-2-[2,2,3,3,4,4,5,5,5-nonadeuteriopentanoyl-[[4-[2-(2H-tetrazol-5-yl)phenyl]phenyl]methyl]amino]butanoic acid
pharmaceutical reference standard
Phenyl (3R,4R)-4-(3-isopropoxyphenyl)-3,4-dimethylpiperidine-1-carboxylate
pharmaceutical reference standard
Octreotide Impurity 13
pharmaceutical reference standard
Alogliptin Impurity 14
pharmaceutical reference standard
methyl (2S)-3-methyl-2-[pentanoyl-[[4-[2-(2H-tetrazol-5-yl)phenyl]phenyl]methyl]amino]butanoate
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