Category
Xanomeline
CAS Number
NA
Molecular Formula
C₈H₁₁N₃OS
Molecular Weight
197.3 g/mol
Synonym

4-(1-Methyl-1,2,5,6-tetrahydropyridin-3-yl)-1,2,5-thiadiazol-3-ol ; 

Keywords
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.

Xanomeline Alcohol Impurity (CAS No. Not Available), with a Molecular Formula of C₈H₁₁N₃OS and Molecular Weight of approximately 197.26 g/mol, is a Xanomeline-related impurity reference standard used in pharmaceutical API impurity profiling, process-related impurity identification, related substances analysis, analytical method development, and quality control testing. Manasa Life Sciences, a pharmaceutical impurity reference standards manufacturer and supplier in India, offers Xanomeline Alcohol Impurity Analytical Reference Standard for API manufacturers, pharmaceutical companies, CROs, CDMOs, and analytical research laboratories. This Xanomeline Alcohol Impurity Standard supports HPLC analysis, LC-MS/MS characterization, impurity identification, stability studies, and analytical method validation, helping laboratories evaluate the purity and quality of Xanomeline drug substances. Product-specific documentation, including Certificate of Analysis (COA), SDS/MSDS, chromatographic purity data, and analytical characterization reports, may be available upon request, subject to availability.