Betaxolol EP Impurity A
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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.

67193-95-7Betaxolol EP Impurity A

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Catalogue No.:VL2940005
CAS No.:67193-95-7
Mol. Formula:C14H23NO2
Mol. Weight:237.34 g/mol

Additional information on CAS 67193-95-7

Parent drug

Betaxolol

IUPAC Name

(2RS)-1-(4-Ethylphenoxy)-3-[(1-methylethyl)amino] propan-2-ol

Pharmacopoeial Synonyms

Betaxolol Related Compound A

Other Synonyms

1-(4-Ethylphenoxy)-3-(isopropylamino)-2-propanol; 1-(4-ethylphenoxy)-3-[(propan-2-yl)amino]propan-2-ol

Smiles

CCC1=CC=C(C=C1)OCC(CNC(C)C)O

InChI

InChI=1S/C14H23NO2/c1-4-12-5-7-14(8-6-12)17-10-13(16)9-15-11(2)3/h5-8,11,13,15-16H,4,9-10H2,1-3H3

Description

Betaxolol EP Impurity A (Free Base), also known as Betaxolol Related Compound A, 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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