Category
Flutamide
CAS Number
98-16-8
Molecular Formula
C₇H₆F₃N
Molecular Weight
161.12 g/mol
Synonym

3-Aminobenzotrifluoride; 3-(Trifluoromethyl)benzenamine; α,α,α-Trifluoro-m-toluidine; 1-Amino-3-(trifluoromethyl)benzene; 3-(Trifluoromethyl)benzenamine; 3-(Trifluoromethyl)phenylamine; 3-Amino-α,α,α-trifluorotoluene; m-(Trifluoromethyl)aniline; m-Amino-α,α,α-trifluorotoluene; m-Aminobenzal Fluoride; m-Aminobenzotrifluoride; m-Trifluoromethylaniline; α,α,α-Trifluoro-m-toluidine; 3-(Trifluoromethyl)aniline (USP)

Keywords
Intermediates
Pharmaceutical Standards
Amines
Aromatics
Fine Chemicals
Mutagenesis Research Chemicals
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.

Flutamide EP Impurity D is also known as Flutamide Impurity D CAS No.: 98-16-8, Molecular Formula: C₇H₆F₃N, Molecular Weight: 161.12 g/mol. Flutamide EP Impurity D is a pharmaceutical analytical reference standard used for impurity profiling, method development, method validation, stability studies, and quality control testing using analytical techniques such as HPLC, LC-MS, Mass Spectrometry (MS), and NMR spectroscopy. It supports pharmaceutical research and development by providing reliable reference material for analytical applications. Manasa Life Sciences, a reputable manufacturer in India, supplies high-quality certified reference materials accompanied by comprehensive documentation, including Certificate of Analysis (CoA), Material Safety Data Sheet (MSDS)/Safety Data Sheet (SDS), and supporting quality documentation. The company's quality systems are designed to support Good Laboratory Practice (GLP), Good Manufacturing Practice (GMP), and Good Distribution Practice (GDP) requirements, with documentation intended to facilitate analytical testing and regulatory submissions. Product information and supporting documentation are prepared in accordance with applicable international pharmaceutical quality expectations and are designed to support laboratories working under guidelines published by the International Council for Harmonisation (ICH), the European Medicines Agency (EMA), the U.S. Food and Drug Administration (FDA), the United States Pharmacopeia (USP), and the European Pharmacopoeia (EP), where applicable.