Amylmetacresol EP Impurity C

We will provide complete documentation support for every Standard Material. All analytical reports such as ¹H NMR, ¹³C NMR, Mass, FT-IR, HPLC Purity/GC Purity/QNMR Purity, Water content by KF/ Loss on Drying/TGA (Thermo-gravimetric Analysis). Certificate of Analysis with potency report. Each Standard Material SER (Structure Elucidation Report) with NMR, Mass, IR spectral interpretation. This whole analytical document can be included in eCTD, ANDA, DMF submissions to regulatory agencies.

Amylmetacresol EP Impurity C is a pharmaceutical impurity reference standard used for impurity profiling, related substance analysis, HPLC, LC-MS/MS, and pharmaceutical quality control. With CAS No. NA, molecular formula C₁₂H₁₈O, and molecular weight 178.3 g/mol, it supports impurity identification, quantification, analytical method development, validation, and stability studies. Manasa Life Sciences is a leading manufacturer and supplier, offering synthesis research and development, custom impurity synthesis, analytical characterization, and structural elucidation with the expertise of expert scientists, along with comprehensive documentation such as Potency/COA, NMR, QNMR, FTIR, GC, SER, MSDS, and regulatory documents.

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