باب
Flutamide
رقم CAS
13312-12-4
الصيغة الجزيئية
C₁₀H₉F₃N₂O₃
وزن جزيئي
262.2 g/mol
مرادف

N-[4-Nitro-3-(trifluoromethyl)phenyl]propanamide;N-[4-Nitro-3-(trifluoro-methyl)phenyl]propanamide; Propanamide, N-[4-nitro-3-(trifluoromethyl)phenyl]-; m-Propionotoluidide, α,α,α-trifluoro-4′-nitro-; Propionyl Analog; N-[4-Nitro-3-(trifluoromethyl) phenyl]propionamide (USP);

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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.

Flutamide EP Impurity C (CAS No. 13312-12-4) is a high-purity European Pharmacopoeia (EP) impurity reference standard manufactured by Manasa Life Sciences. With the molecular formula C₁₀H₉F₃N₂O₃ and a molecular weight of 262.2 g/mol, it is widely used for related substances analysis, HPLC impurity testing, analytical method validation, LC-MS characterization, pharmaceutical quality control, stability studies, and regulatory compliance.

Each batch is supplied as a Certified Reference Material (CRM) with a comprehensive Certificate of Analysis (CoA), including HPLC purity, LC-MS, and NMR characterization data to ensure traceability, reliability, and batch-to-batch consistency. Manufactured in accordance with ICH, EP, USP, US FDA, EMA, and GMP guidelines, this certified reference standard is ideal for pharmaceutical research, API testing, analytical method development, and quality assurance.