Reliable impurity analysis is essential for pharmaceutical quality control. For APIs such as Trimebutine, well-characterised reference standards help laboratories identify and quantify related impurities while supporting analytical method development, validation, and routine testing. Understanding N-Desmethyl Trimebutine Hydrochloride
N-Desmethyl Trimebutine Hydrochloride, also known as Nortrimebutine Hydrochloride or Trimebutine EP Impurity E HCl, is an important pharmaceutical impurity and a major N-demethylated metabolite of Trimebutine.
With a molecular formula of C₂₁H₂₈ClNO₅ and a molecular weight of 409.9 g/mol, it is categorised as an API Working Standard / Pharmaceutical Impurity.
ADVENT's Focus on Analytical Reliability
ADVENT has developed this compound as a pharmaceutical reference standard, emphasising identity confirmation, purity, and analytical reliability.
The material is characterised using:
HPLC — Chromatographic purity assessment
Mass Spectrometry (MS) — Molecular mass confirmation
¹H NMR Spectroscopy — Structural elucidation
FT-IR Spectroscopy — Functional group identification
Applications Across the Analytical Workflow
Trimebutine-related impurity identification and quantification
Analytical method development and validation
Routine quality control and impurity profiling
Working/reference standard applications
Ready to Support Your Analytical Programme
N-Desmethyl Trimebutine Hydrochloride (CAS No. 294882-33-0; Product Code: 55053) supports pharmaceutical manufacturers and analytical laboratories in Trimebutine impurity assessment.
Contact ADVENT for product specifications, analytical documentation, and availability details.
Reliable reference standards. More confident analytical results.
