Betaxolol EP Impurity C
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Documentation

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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.

63659-17-6Betaxolol EP Impurity C

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Catalogue No.:VE007363
CAS No.:63659-17-6
Mol. Formula:C15H20O3
Mol. Weight:248.32 g/mol

Additional information on CAS 63659-17-6

Parent drug

Betaxolol

IUPAC Name

(2RS)-2-[[4-[2-(Cyclopropylmethoxy)ethyl]phenoxy]-methyl]oxirane ;

Pharmacopoeial Synonyms

Betaxolol Oxirane Analog

Other Synonyms

[[4-[2-(Cyclopropylmethoxy)ethyl]phenoxy]methyl]oxirane

Smiles

C1CC1COCCC2=CC=C(C=C2)OCC3CO3

InChI

InChI=1S/C15H20O3/c1-2-13(1)9-16-8-7-12-3-5-14(6-4-12)17-10-15-11-18-15/h3-6,13,15H,1-2,7-11H2

Description

Betaxolol EP Impurity C (Free Base), also known as Betaxolol Oxirane Analog, in various pharmacopoeias, is a highly characterized standard. It meets strict regulatory requirements set by USP, EMA, JP, and BP, making it a crucial component in Abbreviated New Drug Applications (ANDA), New Drug Applications (NDA), and the commercial production of Betaxolol. To ensure precision and reliability in analytical applications, this impurity standard is supplied with a detailed Structure Elucidation Report (SER), offering valuable insights for method development and quality control.

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