Keywords

• Faropenem daloxate
• Faropenem medoxil
• Faropenem medoxomil

Quick Details

• ProName: Faropenem daloxate 141702-36-5
• CasNo: 141702-36-5
• Molecular Formula: C17H19NO8S
• Appearance: White solid
• Application: Pharmaceutical research
• DeliveryTime: prompt delivery
• PackAge: Screw bottle,foil bags,Reagent bottles
• Port: shenzhen/hongkong
• ProductionCapacity: 5000 Metric Ton/Year
• Purity: 95%+
• Storage: cool and dry
• Transportation: DHL,FedEx,UPS,EMS,TNT;
• LimitNum: 1 Kilogram
• Moisture Content: 0.1%
• Impurity: 0.1%

Superiority

We supply over 20000 types of spot impurity reference materials, with sufficient supply and same day delivery to meet customers' urgent needs for replenishment at any time. The company has its own research and development center and laboratory, and the team members have over ten years of experience in developing drug impurity reference standards. Our website www.molcoo.com covers over 98% of cutting-edge generic drug projects, with complete structural formulas that greatly save customers time in impurity structure analysis and inference. All products undergo strict quality control testing and provide relevant information such as COA, H-NMR, C-NMR, MS/GC-MS, HPLC/GC purity, QNMR quantification, TGA thermogravimetric analysis, IR infrared, UV ultraviolet, two-dimensional (COSY, NOESY, HMBC, HMQC), etc. These structural confirmation spectra ensure quality and reliability. Our products have a wide range of categories, fast delivery time, good quality, and low prices, which can quickly solve various customer needs such as replenishment and consistency evaluation.

Details

Faropenem Esters Impurity Reference Standards – Accelerating Drug Development & Quality Control

Product Overview
Faropenem Esters, derivatives of Faropenem, are penem-class antibiotics that inhibit bacterial cell wall synthesis, making them effective against drug-resistant infections. To meet the needs of drug R&D, quality analysis, and bioequivalence studies, we offer high-purity Faropenem Esters impurity reference standards, including popular impurities like Impurity 2 (CAS: 106560-13-8), Impurity 18 (CAS: 1690457-78-3), and Impurity 7 (CAS: 120705-68-2).

Key Features

• High Purity: HPLC purity ≥95%, with select batches reaching 98%+. COA reports, HNMR, MS, and HPLC spectra provided.
• Comprehensive Structural Verification: IR, UV, and 2D NMR (COSY, NOESY, HMBC, HMQC) data for unambiguous impurity identification.
• In-Stock Availability: Multiple packaging options (10mg–100g) with expedited shipping for urgent requests.
• Regulatory Support: Impurity source analysis, QC strategy development, and analytical method optimization services.

Applications

• Drug Discovery: Impurity structural elucidation, metabolite profiling, and degradation pathway studies.
• Quality Control: Impurity limit determination, stability testing, and lot-to-lot consistency evaluation.
• Bioequivalence: Impurity spectrum comparison for generic drug development.

Technical Expertise

• Over a decade of experience in impurity R&D, with custom synthesis capabilities.
• Advanced SFC purification technology for complex impurity isolation.
• End-to-end solutions including process scale-up and CMC optimization.