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Postion:Product Catalog >Fosfomycin Impurity 28
Fosfomycin Impurity 28
  • Fosfomycin Impurity 28
  • Fosfomycin Impurity 28
  • Fosfomycin Impurity 28
  • Fosfomycin Impurity 28
  • Fosfomycin Impurity 28

Fosfomycin Impurity 28 NEW

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Package 10mg 50mg 100mg
Min. Order: 10mg
Supply Ability: 1000
Update Time: 2025-07-31

Product Details

Product Name: Fosfomycin Impurity 28 CAS No.: 60821-12-7
Min. Order: 10mg Purity: 99%+ HPLC
Supply Ability: 1000 Release date: 2025/07/31
M.W.: C4H11O5P

Fosfomycin Impurity 28;60821-12-7

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WhatsAPP: +86 17386083646
E-mail: anna@molcoo.com

Product Information

  • Product Code:F042028

  • English Name:Fosfomycin Impurity 28

  • English Alias:2-ethoxyethyl dihydrogen phosphate

  • CAS No.:60821-12-7

  • Molecular Formula:C₄H₁₁O₅P

  • Molecular Weight:170.10

Advantages

  • High-Purity Reference Standard:Confirmed by HPLC (≥99.0%), NMR (1H, 13C, 31P), HRMS, and elemental analysis, suitable for Fosfomycin impurity analysis and quality control.

  • Stability Assurance:Stable for 36 months at -20℃ under light-protected, sealed storage; degradation rate <0.3% in methanol-water mixture within 6 months.

Applications

  • Quality Control Testing:Used for UPLC-MS/MS detection of Impurity 28 in Fosfomycin API and formulations, controlling content to meet ICH Q3A standards (single impurity limit ≤0.1%).

  • Process Optimization Research:Monitors impurity formation during Fosfomycin synthesis, reducing generation by >30% by adjusting ethylation temperature (e.g., 40-50℃) and reaction time.

  • Method Validation:Serves as a standard for developing impurity detection methods, verifying UPLC resolution (≥3.0) and LOD (0.01 ng/mL).

Background Description

Fosfomycin, a broad-spectrum antibiotic, inhibits bacterial cell wall synthesis and is used for treating urinary tract infections, respiratory infections, etc. Impurity 28, a process-related impurity in Fosfomycin synthesis, may originate from phosphorylation or etherification side reactions. Its ethoxy and phosphate groups may affect drug water solubility, stability, and antibacterial activity. Strict impurity control for antibiotics is critical to drug quality, making research on this impurity essential.

Research Status

  • Detection Technology:UPLC-MS/MS with C18 column (1.7μm) and 0.1% formic acid-acetonitrile gradient elution achieves separation within 4 minutes, with LOD of 0.005 ng/mL for trace impurity analysis.

  • Formation Mechanism:Formed by esterification of phosphoric acid with 2-ethoxyethanol under acidic catalyst (e.g., sulfuric acid); optimizing catalyst dosage and reaction pH inhibits side reactions.

  • Safety Evaluation:In vitro cytotoxicity shows IC₅₀ of 205.6 μM against Vero cells (Fosfomycin IC₅₀=12.3 μM), with lower toxicity than the main drug but requiring strict content control. Long-term stability testing is ongoing to monitor degradation under high temperature and humidity conditions.

NOTE!

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 17386083646
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! 


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