N-Nitroso-Betaxolol
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Ubicación del inventario

  • New Jersey, USA
  • Czech Republic, EU
  • Mumbai, India

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Documentation

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Incluye: HPLC, MASS/LC-MS, RMN de 1H, FT-IR, potencia, informe de elucidación estructural (SER) y datos analíticos adicionales según el producto.

N-Nitroso-Betaxolol

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Número de catálogo:VE0012730
N.º CAS:N/A
Fórmula mol.::C18H28N2O4
Peso mol.::336.43 g/mol

Información adicional sobre el N-Nitroso-Betaxolol

FDA Potency Category 4 NDSRI

1500 ng/day is the U.S. FDA’s current Acceptable Intake (AI) limit for N-nitroso-betaxolol (NDSRI). Refer to the FDA nitrosamine page for the latest guidance.

Fármaco de origen

Betaxolol

Nombre IUPAC

N-(3-(4-(2-(cyclopropylmethoxy)ethyl)phenoxy)-2-hydroxypropyl)-N-isopropylnitrous amide

Sinónimos farmacopeicos

N/A

Otros sinónimos

N/A

SMILES

O=NN(CC(O)COC1=CC=C(CCOCC2CC2)C=C1)C(C)C

InChl

InChI=1S/C18H28N2O4/c1-14(2)20(19-22)11-17(21)13-24-18-7-5-15(6-8-18)9-10-23-12-16-3-4-16/h5-8,14,16-17,21H,3-4,9-13H2,1-2H3

Descripción

N-Nitroso-Betaxolol is an N-nitroso derivative of the secondary amine present in Betaxolol | which is a highly characterized reference material that meets stringent regulatory standards set for nitrosamine compounds | including those set by USP | EMA | JP | and BP. This nitroso standard is essential for a variety of applications | such as analytical method development | method validation (AMV) | and Quality Control (QC) | particularly in the context of Betaxolol production. It is suitable for use in both Abbreviated New Drug Applications (ANDA) and New Drug Applications (NDA). This nitrosamine standard helps establish detection limits | quantify impurity levels | and ensure trace nitroso impurities in pharmaceutical products remain within FDA and EMA safety limits.

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