Category
Atropine
CAS Number
500-55-0
Alternate CAS Number
5978-81-4 (HCl salt) ; 6020-16-2 (HBr salt)
Molecular Formula
C₁₇H₂₁NO₂
Molecular Weight
271.36 g/mol
Synonym

Hyoscyamine sulfate Impurity G (EP); Atropate-1αH,5αH-tropan-3α-ol; Apoatropin; endo-α-Methylenebenzeneacetic Acid 8-Methyl-8-azabicyclo[3.2.1]oct-3-yl Ester; Apoatropin; Apohyoscyamin; Apohyoscyamine; Atropamin; Atropamine; Atropyltropeine; (1R,3r,5S)-8-methyl-8-azabicyclo[3.2.1]oct-3-yl 2-phenylpropenoate (apoatropine); Apoatropine; (1R ,3r ,5S )-8-Methyl-8-azabicyclo[3.2.1]octan-3-yl 2-phenylacrylate (USP);

Keywords
High-Quality Pharmaceutical Reference Standards
Fine Chemicals
Pharmaceutical Standards
Intermediates
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.

Manasa Lifesciences is a reliable manufacturer and supplier of Atropine EP Impurity A (CAS No. 500-55-0) in India, offering high-quality pharmaceutical impurity reference standards for quality control, analytical testing, impurity profiling, synthesis research, and R&D. Atropine EP Impurity A has the molecular formula C₁₇H₂₁NO₂ and molecular weight 271.36 g/mol. Our expert scientists support comprehensive characterization and documentation, including HPLC, LC-MS/MS, NMR, FTIR, QNMR, potency/assay testing, and COA, with applicable GDP and GLP practices and consideration of relevant ICH, EMA, USP, and EP regulatory and pharmacopoeial requirements. We provide dependable solutions for pharmaceutical research, analytical method development, impurity characterization, quality assurance, and regulatory support.