N-Nitroso Amoxicillin EP Impurity E
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Stock Locations

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

* Stock subject to availability.

Documentation

Download MSDS

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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.

N-Nitroso Amoxicillin EP Impurity E

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Catalogue No.:VE0024324
CAS No.:N/A
Mol. Formula:C15H20N4O5S
Mol. Weight:368.41 g/mol

Additional information on N-Nitroso Amoxicillin EP Impurity E

Parent drug

Amoxicillin

IUPAC Name

(2R, 4S)-2-(((R)-2-amino-2-(4-hydroxyphenyl)acetamido)methyl)-5, 5-dimethyl-3-nitrosothiazolidine-4-carboxylic acid

Pharmacopoeial Synonyms

N/A

Other Synonyms

N/A

Smiles

OC1=CC=C([C@@]([H])(N)C(NC[C@@]2([H])SC(C)(C)[C@]([H])(C(O)=O)N2N=O)=O)C=C1

InChI

InChI=1S/C15H20N4O5S/c1-15(2)12(14(22)23)19(18-24)10(25-15)7-17-13(21)11(16)8-3-5-9(20)6-4-8/h3-6, 10-12, 20H, 7, 16H2, 1-2H3, (H, 17, 21)(H, 22, 23)/t10-, 11-, 12?/m1/s1

Description

N-Nitroso Amoxicillin EP Impurity E is an N-nitroso derivative of the secondary amine present in Amoxicillin | 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 Amoxicillin 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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