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Postion:Product Catalog >Piperacillin Impurity
Piperacillin Impurity
  • Piperacillin Impurity
  • Piperacillin Impurity
  • Piperacillin Impurity
  • Piperacillin Impurity
  • Piperacillin Impurity

Piperacillin Impurity NEW

Price Get Latest Price
Package 10mg 50mg 100mg
Min. Order: 10mg
Supply Ability: 1000
Update Time: 2025-06-13

Product Details

Product Name: Piperacillin Impurity CAS No.: 64817-22-7
Min. Order: 10mg Purity: 99%+ HPLC
Supply Ability: 1000 Release date: 2025/06/13

Piperacillin Impurity; 64817-22-7

Article illustration


  • Product Information (P032043)

  • Product Code: P032043

  • English Name: Piperacillin Impurity 43

  • English Alias: (2R,4S)-2-((R)-carboxy((R)-2-(4-ethyl-2,3-dioxopiperazine-1-carboxamido)-2-phenylacetamido)methyl)-5,5-dimethylthiazolidine-4-carboxylic acid

  • CAS No.: 64817-22-7

  • Molecular Formula: C??H??N?O?S

  • Molecular Weight: 535.57

  • Advantages

  • Strict Structural Confirmation: Confirmed by NMR, HRMS, and elemental analysis with ≥98.5% purity (HPLC), meeting high requirements for Piperacillin impurity analysis.

  • Controllable Stability: Stored at -20℃ in the dark with a shelf life of 36 months; degradation rate <1% in acetonitrile-water solution within 3 months.

  • Applications

  • Antibiotic Quality Research: Used for impurity detection in Piperacillin API and formulations, complying with USP, EP, and other pharmacopoeial standards for β-lactam antibiotics.

  • Methodology Validation: Serves as a reference standard for developing impurity detection methods, verifying HPLC specificity and sensitivity (LOQ 0.1 μg/mL).

  • Background Description

  • Piperacillin, a broad-spectrum semi-synthetic penicillin, may generate Impurity 43 from side chain condensation or piperazine ring oxidation. With complex structure and multiple chiral centers, this impurity may affect the drug's antibacterial activity and safety. As antibiotic impurity control standards improve, studying such complex impurities is key to ensuring drug quality.
  • Research Status

  • Detection Technology: HPLC-UV (220nm) with C18 column (5μm) and phosphate buffer-acetonitrile gradient elution, achieving resolution >2.0 and LOQ 0.5 μg/mL.

  • Formation Mechanism: Results from side reactions between Piperacillin side chain and 4-ethyl-2,3-dioxopiperazine intermediates; optimizing acylation reaction pH (7.0-7.5) reduces impurity generation by >50%.

  • We can also customize related analogues and modified peptides including HPLC, MS, 1H-NMR, MS, HPLC, IR, UV, COA, MSDS.
    This product is intended for laboratory use only!

    WhatsAPP: +86 17320513646
    E-mail: anna@molcoo.com


    NEW IN STOCK!

    The Molcoo Laboratory added drug impurity reference standards, including Baricitinib, Piperazine, Benzylpenicillin, Tranilast and multiple N-Nitroso drug impurities! Now available for immediate delivery! 





Company Profile Introduction

1. Drug standards and drug impurity reference substances: provide more than 20,000 kinds of spot impurity reference substances, with sufficient supply and same-day delivery. We have a professional R&D team and comprehensive quality control testing to ensure product quality and reliability. 2. Customized synthesis of impurities and new molecules: Quickly respond to the customized needs of CDE impurities, stably supply impurities that have established quality standards, and provide customized synthesis services for new compounds in the research and development of innovative drugs. 3. Preparation and separation of unknown impurities: With a professional impurity preparation and separation technical team and SFC preparation and separation instruments, we can solve the problems of impurity preparation in complex projects. 4. Process development of new drug intermediates: provide the supply of new drugs and new molecular impurities, process optimization services, as well as the screening and impurity analysis of commercialization routes. 5. Peptide synthesis: Provide customized peptide synthesis services, and cover all kinds of degradation impurities and process impurities generated in the research and development of peptide drugs. At the same time, it provides comprehensive structural confirmation data and customized testing services.

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