Category
Amorolfine
CAS Number
2134097-34-8
Molecular Formula
C₂₁H₃₅NO
Molecular Weight
317.51 g/mol
Synonym

(2S,6S)-2,6-dimethyl-4-[2-methyl-3-[4-(2-methylbutan-2-yl)phenyl]propyl]morpholine; Mixture of (2RS,6RS)-2,6-Dimethyl-4-[(2R)-2-methyl-3-[4-(2-methylbutan-2-yl)phenyl]propyl]morpholine and (2RS,6RS)-2,6-dimethyl-4-[(2S)-2-methyl-3-[4-(2-methylbutan-2-yl)phenyl]propyl]morpholine

Keywords
High-Quality Pharmaceutical Reference Standards
Impurities
Metabolites.
Pharmaceutical Standards
Fine Chemicals
Impurities Manufacturer in India
Impurities manufacturer and Suppliers in Hyderabad india
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Purity:

Above - 95.0%

Technical Data:

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.

Amorolfine EP Impurity E (CAS No. 2134097-34-8) is a pharmaceutical impurity reference standard with the molecular formula C₂₁H₃₅NO and molecular weight 317.51 g/mol, used in pharmaceutical impurity profiling, related-substances analysis, drug substance characterization, analytical research, and quality control testing. It supports applications such as HPLC analysis, LC-MS identification, analytical method development, method validation, stability-indicating studies, degradation-product assessment, and impurity monitoring. Manasa Life Sciences is an India-based manufacturer and supplier of pharmaceutical impurities, analytical reference standards, and research compounds, serving pharmaceutical manufacturers, CROs, QC laboratories, and R&D organizations. With expert scientific support and advanced analytical capabilities, Manasa Life Sciences can provide characterization data including HPLC, LC-MS, ¹H NMR, ¹³C NMR, GC, and TGA, supporting analytical method optimization, impurity identification, specification development, quality assessment, and regulatory documentation in accordance with applicable ICH, EMA, EP, and USP requirements.