Description

Nilutamide CAS NO 63612-50-0 is a non-steroidal antiandrogen pharmaceutical compound used primarily in the treatment of prostate cancer. It functions by competitively inhibiting androgen binding to its receptor, thereby blocking the growth-stimulating effects of androgens on cancerous cells. This product is essential for pharmaceutical manufacturers and research institutions developing advanced oncological therapies and conducting hormone-related biochemical studies.

Application

• Pharmaceutical Active Ingredient (API): Primary use in the formulation of anti-prostate cancer medications.
• Hormone Therapy Research: A key compound in preclinical and clinical studies investigating androgen receptor antagonists.
• Biochemical Standard: Serves as a reference standard in analytical laboratories for quality control and method validation.
• Oncology Drug Development: Used in R&D for developing new combination therapies and dosage forms for hormone-sensitive cancers.

Basic Information

Product Name	Nilutamide
CAS No.	63612-50-0
Molecular Formula	C12H10F3N3O4
Molecular Weight	317.22 g/mol
Synonyms	5,5-Dimethyl-3-[4-nitro-3-(trifluoromethyl)phenyl]imidazolidine-2,4-dione; RU 23908; Anandron; Nilandron; Nilutamida; Nilutamidum; Nilutamid; Nilutamid
EINECS	Contact for details

Quality Control

Our Nilutamide is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing including identification, assay, impurity profiling, and residual solvent analysis to ensure it meets high-purity standards suitable for pharmaceutical applications. A Certificate of Analysis (COA) detailing all test results is provided with every shipment.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at controlled room temperature (15-25°C). Due to its hygroscopic nature, the container must be kept tightly sealed in a dry environment to prevent moisture absorption.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to reference spectrum
Identification (HPLC)	Retention time corresponds to reference standard
Assay (HPLC)	98.0% - 102.0% (on anhydrous basis)
Related Substances (HPLC)	Individual impurity: NMT 0.5% Total impurities: NMT 1.5%
Water Content (KF)	NMT 0.5%
Residue on Ignition	NMT 0.1%
Heavy Metals	NMT 20 ppm

Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.