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(5-Dimethylaminocarbonylpyrrolidin-3-Ylthio)-6-(1-Hydroxyethyl)Penem-3-Carboxylic Acid CAS NO 96036-10-1


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CAS No.:96036-10-1

Grade:Pharmacy Grade

Content:99.9%

Brand:Customizable

Packaging:Customizable

Description

(5-Dimethylaminocarbonylpyrrolidin-3-Ylthio)-6-(1-Hydroxyethyl)Penem-3-Carboxylic Acid is a key advanced pharmaceutical intermediate belonging to the penem class of β-lactam antibiotics. This compound is critical for the research and development of novel antibacterial agents, offering a sophisticated structural platform for further chemical modification. It is primarily utilized by pharmaceutical R&D laboratories and fine chemical manufacturers engaged in the synthesis of next-generation antibiotics to combat resistant bacterial strains.

Application

  • Pharmaceutical Intermediate: A crucial building block in the synthesis of novel penem-based antibiotic candidates.
  • Antibacterial Research: Serves as a core scaffold in medicinal chemistry programs aimed at developing new mechanisms of action against resistant bacteria.
  • Fine Chemical Synthesis: Used in multi-step organic synthesis for creating complex, high-value active pharmaceutical ingredients (APIs).
  • Biochemical Studies: Employed in research to study β-lactamase inhibition and bacterial cell wall synthesis.
  • Process Development: Used in scaling up and optimizing manufacturing routes for advanced antibiotic compounds.

Basic Information

Product Name (5-Dimethylaminocarbonylpyrrolidin-3-Ylthio)-6-(1-Hydroxyethyl)Penem-3-Carboxylic Acid
CAS No. 96036-10-1
Molecular Formula C16H23N3O5S
Molecular Weight 369.44 g/mol
Synonyms FCE 22101; (5-Dimethylaminocarbonylpyrrolidin-3-ylthio)-6-(1-hydroxyethyl)penem-3-carboxylic acid; 6-(1-Hydroxyethyl)-2-[(3S,5S)-5-(dimethylcarbamoyl)pyrrolidin-3-yl]sulfanyl-1-azabicyclo[3.2.0]hept-2-ene-7-one-3-carboxylic acid; FCE-22101; Faropenem Intermediate; Penem Derivative
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Quality Control

Our production of this high-purity pharmaceutical intermediate adheres to strict quality management systems. Every batch is subjected to comprehensive analytical testing, including HPLC, NMR, and MS, to ensure identity, purity, and consistency. A detailed Certificate of Analysis (COA) is provided with each shipment, confirming compliance with agreed specifications. We support development and commercial projects requiring material that meets GMP-grade standards for advanced pharmaceutical synthesis.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at a controlled room temperature (15-25°C). This compound is hygroscopic (moisture-sensitive) and must be kept under an inert atmosphere (e.g., nitrogen or argon) in its original packaging to prevent degradation. For long-term storage, consider freezing at -20°C.

Specification

Item Specification
Appearance White to off-white powder
Identification (HPLC) Conforms to reference standard
Identification (IR) Conforms to structure
Assay (HPLC) ≥ 98.0%
Water Content (KF) ≤ 1.0%
Residue on Ignition ≤ 0.1%
Related Substances (HPLC) Total impurities ≤ 2.0% Any single impurity ≤ 0.5%

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

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Each batch undergoes strict QC, accompanied by COA, MSDS, and full compliance with international standards.

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