Description

Lufuradom is a synthetic chemical compound belonging to the benzodiazepine class, identified by CAS No. 85118-42-9. It is valued in research and development for its specific pharmacological profile and serves as a key intermediate in the synthesis of more complex active pharmaceutical ingredients (APIs). This compound is primarily utilized by pharmaceutical R&D laboratories and fine chemical manufacturers focused on neuropharmacology and central nervous system (CNS) drug discovery.

Application

• Pharmaceutical Intermediate: Serves as a critical building block in the multi-step synthesis of novel benzodiazepine derivatives and related therapeutic agents.
• Research & Development: Used in preclinical studies and pharmacological research to investigate structure-activity relationships (SAR) within the benzodiazepine receptor family.
• Reference Standard: Employed as an analytical standard in quality control laboratories for method development and impurity profiling.
• Fine Chemical Synthesis: Acts as a specialized intermediate for contract research organizations (CROs) and custom synthesis operations.

Basic Information

Product Name	Lufuradom
CAS No.	85118-42-9
Molecular Formula	C₁₇H₁₄ClFN₂O
Molecular Weight	316.76 g/mol
Synonyms	Lufuradom; 7-Chloro-5-(2-fluorophenyl)-1,3-dihydro-1-methyl-2H-1,4-benzodiazepin-2-one; 85118-42-9; Lufuradom (Benzodiazepine); 1-Methyl-7-chloro-5-(2-fluorophenyl)-1,3-dihydro-2H-1,4-benzodiazepin-2-one; Ro 11-6896; Ro-11-6896
EINECS	Contact for details

Quality Control

Our Lufuradom is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing, including identification, purity assay, and impurity profiling via techniques such as HPLC, NMR, and mass spectrometry, to ensure it meets the stringent requirements for research and synthesis. A Certificate of Analysis (COA) detailing all specifications and results is provided with every shipment.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated area at controlled room temperature (typically 15-25°C). Keep the container tightly sealed to protect from moisture.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to structure
Identification (HPLC)	Retention time matches reference standard
Purity (HPLC)	≥ 98.0%
Related Substances (HPLC)	Any individual impurity ≤ 0.5%
Total Impurities	≤ 2.0%
Loss on Drying	≤ 0.5%
Residue on Ignition	≤ 0.1%

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