N-Nitroso Formoterol
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  • New Jersey, USA
  • Czech Republic, EU
  • Mumbai, India

* Stock subject to availability.

Documentation

Download MSDS

Download Sample COA

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

N-Nitroso Formoterol

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Catalogue No.:VE0014176
CAS No.:N/A
Mol. Formula:C19H23N3O5
Mol. Weight:373.41 g/mol

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UNIT PRICE QTY STATUS ACTION
100 mg $499.00
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Additional information on N-Nitroso Formoterol

Parent drug

Formoterol

IUPAC Name

N-(2-Hydroxy-5-((S)-1-hydroxy-2-(((S)-1-(4-methoxyphenyl)propan-2-yl)(nitroso)amino)ethyl)phenyl)formamide

Pharmacopeial Synonyms

N/A

Synonyms

N/A

Smiles

O=CNC1=CC([C@H](O)CN([C@@H](C)CC2=CC=C(OC)C=C2)N=O)=CC=C1O

InChI

InChI=1S/C19H23N3O5/c1-13(9-14-3-6-16(27-2)7-4-14)22(21-26)11-19(25)15-5-8-18(24)17(10-15)20-12-23/h3-8,10,12-13,19,24-25H,9,11H2,1-2H3,(H,20,23)/t13-,19+/m0/s1

FDA Potency Category 4 NDSRI

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

Shipping Condition

Ambient Temperature

Description

N-Nitroso Formoterol is an N-nitroso derivative of the secondary amine present in Formoterol, 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 Formoterol 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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