Olmesartan EP Impurity B
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Includes: HPLC, MASS/LC-MS, 1H NMR, FT-IR, Potency, Structure Elucidation Report (SER), and additional analytical data depending on the product.

849206-43-5Olmesartan EP Impurity B

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Catalogue No.:VL184001
CAS No.:849206-43-5
Mol. Formula:C24H24N6O2
Mol. Weight:428.49 g/mol

Additional information on CAS 849206-43-5

Parent drug

Olmesartan

IUPAC Name

6,6-dimethyl-2-propyl-3-[[2′-(1H-tetrazol-5-yl)biphenyl-4-yl]methyl]-3,6-dihydro-4H-furo[3,4-d]imidazol-4-one

Synonyms

Olmesartan Related Compound A; Olmesartan EP Impurity B; Olmesartan Gama-Lactone; Olmesartan Lactone; Olmesartan Lactone Impurity; 3, 6-Dihydro-6, 6-dimethyl-2-propyl-3-[[2′-(2H-tetrazol-5-yl)[1, 1′-biphenyl]-4-yl]methyl]-4H-Furo[3, 4-d]imidazol-4-one; Olmesartan EP Impurity B;

Description

Olmesartan EP Impurity B (CAS No: 849206-43-5) or Olmesartan Lactone Impurity is an impurity present in olmesartan which is an angiotensin II receptor blocker that selectively blocks the binding of angiotensin 2 to the AT1 receptor in vascular smooth muscle.

References

Srinivasu, Kondra, et al. “Novel Analytical Method Using Acquity QDa Mass Detector Coupled with LC-PDA for Impurity Profiling of Amlodipine Besylate and Olmesartan Medoxomil in Fixed Dose Tablets Formulation.” Saudi Journal of Medical and Pharmaceutical Sciences, vol. 05, no. 10, Oct. 2019, pp. 871–84, https://doi.org/10.36348/sjmps.2019.v05i10.008.?

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