Category
Amorolfine
CAS Number
2109184-47-4
Molecular Formula
C₂₁H₃₅NO₂
Molecular Weight
333.5 g/mol
Synonym

(2RS,4E,6SR)-2,6-dimethyl-4-[(2RS)-2-methyl-3-[4-(2- methylbutan-2-yl)phenyl]propyl]morpholine 4-oxide ; 2,6-Dimethyl-4-(2-methyl-3-(4-(tert-pentyl)phenyl)propyl)morpholine 4-oxide; Morpholine, 4-[3-[4-(1,1-dimethylpropyl)phenyl]-2-methylpropyl]-2,6-dimethyl-, 4-oxide;Amorolfine N-Oxide;

Keywords
High-Quality Pharmaceutical Reference Standards
Intermediates
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 A (CAS No. 2109184-47-4) is a pharmaceutical impurity reference standard with the molecular formula C₂₁H₃₅NO₂ and molecular weight 333.5 g/mol, suitable for pharmaceutical impurity profiling, related-substance analysis, drug substance characterization, analytical testing, and quality control applications. This impurity standard is valuable for HPLC impurity analysis, LC-MS characterization, analytical method development, method validation, stability studies, degradation-product evaluation, and pharmaceutical R&D. Manasa Life Sciences is a trusted India-based manufacturer and supplier of pharmaceutical impurities, analytical reference standards, and research compounds, supporting pharmaceutical manufacturers, CROs, QC laboratories, and research organizations with reliable analytical solutions. Our expert scientific team can support chromatographic analysis, impurity identification, analytical data generation, specification testing, and regulatory documentation, with characterization techniques including HPLC, LC-MS, ¹H NMR, ¹³C NMR, GC, and TGA, aligned with applicable ICH, EMA, EP, and USP requirements.