Category
Amorolfine
CAS Number
2714893-32-8
Molecular Formula
C₂₁H₃₅NO
Molecular Weight
317.52 g/mol
Synonym

(2RS,6SR)-2,6-Dimethyl-4-[(2RS)-2-methyl-3-[3-(2-methylbutan-2-yl)phenyl]propyl]morpholine ; Morpholine, 4-[3-[3-(1,1-dimethylpropyl)phenyl]-2-methylpropyl]-2,6-dimethyl-, (2R,6S)-rel; meta-Amorolfine;

Keywords
Fine Chemicals
Pharmaceutical Standards
Metabolites.
Impurities
Intermediates
High-Quality Pharmaceutical Reference Standards
Impurities Manufacturer in India
Impurities manufacturer and Suppliers in Hyderabad india
Slide_1
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 J (CAS No. 2714893-32-8; Molecular Formula: C₂₁H₃₅NO; Molecular Weight: 317.52 g/mol) is a high-purity Amorolfine related substance and pharmaceutical impurity reference standard intended for impurity profiling, related compound identification, process-related impurity assessment, drug substance characterization, degradation product analysis, chromatographic purity testing, HPLC/LC-MS analysis, analytical method development, and stability-indicating studies. Manasa Life Sciences, a trusted pharmaceutical impurity manufacturer and supplier in Hyderabad, India, offers Amorolfine EP Impurity J reference standards, Amorolfine related compounds, process impurity markers, pharmaceutical analytical standards, API characterization materials, degradation product standards, and impurity profiling reference materials for pharmaceutical R&D, QC laboratories, CROs, and analytical testing applications worldwide. Products are supported with COA, MSDS, SDS, and relevant technical documentation, with quality practices aligned with applicable GMP, GDP, ICH, USFDA, USP, EP, and EMA requirements.