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Bis-Linezolid CAS NO 908143-04-4


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CAS No.:908143-04-4

Grade:Pharmacy Grade

Content:99.9%

Brand:Customizable

Packaging:Customizable

Description

Bis-Linezolid CAS NO 908143-04-4 is a key pharmaceutical intermediate, specifically a dimeric derivative of the oxazolidinone antibiotic linezolid. This compound is of significant value in the synthesis and research of advanced antibacterial agents, offering a structural platform for developing novel therapeutics. It is primarily required by pharmaceutical manufacturers and research institutions engaged in the development of next-generation antibiotics and complex active pharmaceutical ingredients (APIs).

Application

  • Pharmaceutical Intermediate: Serves as a critical building block in the synthesis of novel oxazolidinone-class antibiotics and related compounds.
  • Antibacterial Research: Used in medicinal chemistry research for structure-activity relationship (SAR) studies to develop new antibacterial agents with improved efficacy.
  • API Development: Employed in the process development and scale-up manufacturing of complex active pharmaceutical ingredients.
  • Reference Standard: Can be utilized as a reference standard or impurity marker in analytical method development and quality control for linezolid-based products.
  • Chemical Synthesis: Acts as a specialized synthon in organic synthesis for constructing complex molecular architectures containing the oxazolidinone pharmacophore.

Basic Information

Product Name Bis-Linezolid
CAS No. 908143-04-4
Molecular Formula Contact for details
Molecular Weight Contact for details
Synonyms Linezolid Dimer; (S)-N-({3-[3-Fluoro-4-(morpholin-4-yl)phenyl]-2-oxo-1,3-oxazolidin-5-yl}methyl)acetamide Dimer; Bis[(5S)-3-[3-Fluoro-4-(4-morpholinyl)phenyl]-2-oxo-5-oxazolidinyl]methyl] Ester; Oxazolidinone Dimer Intermediate; Zyvox Dimer Intermediate
EINECS Contact for details

Quality Control

Our Bis-Linezolid is produced under strict quality management systems to ensure high purity and batch-to-batch consistency. The product undergoes rigorous analytical testing, including HPLC for assay and purity determination, to meet the stringent requirements of pharmaceutical R&D and manufacturing. A comprehensive Certificate of Analysis (COA) detailing identity, purity, and impurity profiles is provided with each batch to support your quality and regulatory documentation.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated area at controlled room temperature (15-25°C). Due to its hygroscopic nature, the container must be kept tightly sealed to prevent moisture absorption, which may affect stability and handling properties.

Specification

Item Specification
Appearance White to off-white powder
Identification (IR) Conforms
Assay (HPLC) ≥ 98.0%
Related Substances (HPLC) Total impurities ≤ 2.0% Any single impurity ≤ 1.0%
Water Content (KF) ≤ 1.0%
Residue on Ignition ≤ 0.1%

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

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