Category
Amorolfine
CAS Number
NA
Molecular Formula
C₂₁H₃₃NO₃
Molecular Weight
347.5 g/mol
Synonym

2-[(2RS)-3-[(2RS,6SR)-2,6-Dimethylmorpholin-4-yl]-2-methylpropyl]-5-(2-methylbutan-2-yl)phenol ;  

Keywords
Fine Chemicals
Pharmaceutical Standards
Metabolites.
Impurities
Intermediates
High-Quality Pharmaceutical Reference Standards
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 H (CAS No.: N/A; Molecular Formula: C₂₁H₃₃NO₃; Molecular Weight: 347.50 g/mol) is a high-purity Amorolfine related substance and pharmaceutical impurity reference material used for impurity profiling, drug substance characterization, related substances testing, process impurity evaluation, degradation assessment, chromatographic analysis, HPLC/LC-MS testing, analytical method development, and stability studies. Manasa Life Sciences, a trusted pharmaceutical impurity standard manufacturer and supplier in Hyderabad, India, provides Amorolfine EP Impurity H reference standards, Amorolfine related compounds, process-related impurity standards, degradation product reference materials, API characterization standards, pharmaceutical analytical compounds, and impurity profiling materials for pharmaceutical R&D, QC laboratories, CROs, and analytical research worldwide. Products are supplied with COA, MSDS, SDS, and supporting technical documentation, supporting applicable GMP, GDP, ICH, USFDA, USP, EP, and EMA quality and regulatory requirements.