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Di(Cefuroxime Ethyl) Ether CAS NO 1202925-10-7


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CAS No.:1202925-10-7

Grade:Pharmacy Grade

Content:99.9%

Brand:Customizable

Packaging:Customizable

Description

Di(Cefuroxime Ethyl) Ether is a key chemical intermediate derived from the cefuroxime antibiotic structure. This compound is of significant value in the pharmaceutical industry for the synthesis of advanced cephalosporin derivatives and other active pharmaceutical ingredients (APIs). It is primarily utilized by research institutions, fine chemical manufacturers, and pharmaceutical companies engaged in the development and production of novel antibacterial agents. Its role as a specialized building block enables the creation of compounds with potentially enhanced efficacy and stability.

Application

  • Pharmaceutical Intermediate: A critical building block in the synthesis of advanced cephalosporin antibiotics and related β-lactam compounds.
  • API Development: Used in research and development for creating new active pharmaceutical ingredients with targeted antibacterial properties.
  • Fine Chemical Synthesis: Serves as a specialized precursor in multi-step organic syntheses for complex molecules.
  • Biochemical Research: Employed in studies investigating structure-activity relationships (SAR) of antibiotic analogs.
  • Process Chemistry: Utilized in scale-up and optimization of manufacturing routes for antibiotic drugs.

Basic Information

Item Details
Product Name Di(Cefuroxime Ethyl) Ether
CAS No. 1202925-10-7
Molecular Formula Contact for details
Molecular Weight Contact for details
Synonyms Bis(cefuroxime ethyl) ether; Cefuroxime ethyl ether dimer; 1,1'-[Oxybis(ethane-2,1-diyl)]bis[(6R,7R)-3-[(carbamoyloxy)methyl]-7-[[(2Z)-2-(2-furyl)-2-(methoxyimino)acetyl]amino]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate]; Cefuroxime Axetil Impurity; Cefuroxime Axetil Related Compound
EINECS Contact for details

Quality Control

Our Di(Cefuroxime Ethyl) Ether is produced under a strict quality management system. Each batch undergoes comprehensive analytical testing, including HPLC for purity and identity confirmation, to ensure it meets the stringent requirements for pharmaceutical intermediates. Certificates of Analysis (COA) are provided with every shipment, detailing all relevant specifications. We adhere to cGMP principles where applicable to guarantee consistent quality and traceability.

Storage

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

Specification

Item Specification
Appearance White to off-white powder
Identification (HPLC/IR) Conforms to reference standard
Assay (HPLC) ≥ 95.0%
Related Substances (HPLC) Total impurities ≤ 5.0%
Water Content (KF) ≤ 2.0%
Residual Solvents (GC) Complies with ICH guidelines

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

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