Category
Amorolfine
CAS Number
67468-13-7
Molecular Formula
C₂₁H₃₅NO
Molecular Weight
317.52 g/mol
Synonym

(2RS,6SR)-2,6-Dimethyl-4-[(2RS)-2-methyl-3-[4-(3-methylbutan-2-yl)phenyl]propyl]morpholine ; 4-[3-[4-(1,2-Dimethylpropyl)phenyl]-2-methylpropyl]-2,6-dimethyl-morpholine; 2,6-Dimethyl-4-(2-methyl-3-(4-(3-methylbutan-2-yl)phenyl)propyl)morpholine; Desmethyl Methylbutyl Amorolfine;

Keywords
Fine Chemicals
Pharmaceutical Standards
Metabolites.
Impurities
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 I (CAS No. 67468-13-7; Molecular Formula: C₂₁H₃₅NO; Molecular Weight: 317.52 g/mol) is a high-purity Amorolfine related compound and pharmaceutical impurity reference standard used for impurity identification, related substances analysis, process impurity monitoring, drug substance characterization, degradation studies, chromatographic purity testing, HPLC/LC-MS analysis, analytical method development, and stability-indicating studies. Manasa Life Sciences, a trusted API impurity manufacturer and pharmaceutical reference material supplier in Hyderabad, India, provides Amorolfine EP Impurity I reference standards, Amorolfine related substances, process-related impurity standards, degradation product standards, API characterization materials, pharmaceutical analytical standards, and impurity profiling reference materials for pharmaceutical R&D, QC laboratories, CROs, and analytical research worldwide. Products are supplied with COA, MSDS, SDS, and supporting technical documentation, with applicable quality and distribution practices aligned with GMP, GDP, ICH, USFDA, USP, EP, and EMA requirements.