Description

Sobuzoxane is a synthetic organic compound belonging to the class of oxazolidinones, recognized for its role as a key intermediate in advanced pharmaceutical synthesis. Its importance lies in enabling the production of complex active pharmaceutical ingredients (APIs) with high purity and structural specificity, which is critical for therapeutic efficacy and safety. This compound is essential for research institutions and manufacturers in the pharmaceutical and fine chemical industries focused on developing novel therapeutic agents.

Application

• Pharmaceutical Intermediate: A crucial building block in the multi-step synthesis of novel antibiotic and antibacterial agents.
• Antibiotic Research: Serves as a core scaffold for the development of next-generation oxazolidinone-class antibiotics targeting resistant bacterial strains.
• Fine Chemical Synthesis: Used in the preparation of complex chiral molecules requiring the oxazolidinone moiety for stereochemical control.
• Biochemical Research: Employed as a reference standard or reagent in studies investigating bacterial protein synthesis inhibition.
• Process Development: Utilized by process chemists for scaling up and optimizing synthetic routes for pharmaceutical production.

Basic Information

Product Name	Sobuzoxane
CAS No.	98631-95-9
Molecular Formula	C16H21FN2O5
Molecular Weight	340.35 g/mol
Synonyms	(S)-N-{3-[3-Fluoro-4-(4-morpholinyl)phenyl]-2-oxo-5-oxazolidinyl}methyl acetamide; Sobuzoxan; PNU-100592; (S)-N-[[3-[3-Fluoro-4-(morpholin-4-yl)phenyl]-2-oxo-1,3-oxazolidin-5-yl]methyl]acetamide; Linezolid Intermediate; Oxazolidinone Derivative
EINECS	Contact for details

Quality Control

Our Sobuzoxane is manufactured under strict quality management systems to ensure batch-to-batch consistency and high purity, suitable for pharmaceutical R&D and production. Each lot undergoes comprehensive analytical testing, including HPLC for assay and related substances, to meet exacting customer specifications. A Certificate of Analysis (COA) detailing all test results is provided with every shipment to support your quality assurance and regulatory documentation needs.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated area at a 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 reference spectrum
Identification (HPLC)	Retention time corresponds to reference standard
Assay (HPLC)	≥ 98.0%
Related Substances (HPLC)	Total impurities ≤ 2.0% Any single unknown impurity ≤ 0.5%
Water Content (KF)	≤ 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.