Product Data Sheet

Losartan impurity 8

Catalog No. B10711

main product photo
Losartan impurity 8 (O-Acetyl Losartan) is a known impurity of the antihypertensive agent Losartan. It serves as a critical reference standard for quality control and analytical testing in pharmaceutical research. This compound is significant for ensuring the purity and regulatory compliance of Losartan formulations. Its characterization aids in understanding the pharmacological profile and potential impacts of impurities on drug efficacy and safety.
Chemical Information
Catalog NumB10711
M. Wt464.95
FormulaC24H25ClN6O2
Purity>98%
Storageat -20 °C 3 years (powder form); at -20 °C 6 months (Solution base)
CAS No.1006062-27-6
SynonymsO-Acetyl Losartan
SMILESO=C(OCC1=C(Cl)N=C(N1CC=2C=CC(=CC2)C=3C=CC=CC3C4=NN=NN4)CCCC)C
Biological Activity
DescriptionLosartan impurity 8 (O-Acetyl Losartan) is a known impurity of the antihypertensive agent Losartan. It serves as a critical reference standard for quality control and analytical testing in pharmaceutical research. This compound is significant for ensuring the purity and regulatory compliance of Losartan formulations. Its characterization aids in understanding the pharmacological profile and potential impacts of impurities on drug efficacy and safety.
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