CasNo.1703748-89-3,Fosnetupitant 141702-36-5,(1703748-89-3) Suppliers

1 Kilogram	FOB Price: USD 10.0000

Min.Order :1 Kilogram
Purity: 95%+
Payment Terms : T/T,Other

Keywords

Fosnetupitant 1703748-89-3 Fosnetupitant [INN]

Quick Details

Appearance:White solid
Application:Pharmaceutical research
PackAge:Screw bottle,foil bags,Reagent bottles
ProductionCapacity:5000|Metric Ton|Year
Storage:cool and dry
Transportation: DHL,FedEx,UPS,EMS,TNT;

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:

Fosnetupitant Impurity Reference Standards – High-Purity Tools for Drug Development

Product Overview
Fosnetupitant (CAS: 1703748-89-3) is a novel NK1 receptor antagonist prodrug used in the prevention of chemotherapy-induced nausea and vomiting (CINV). To meet the needs of drug R&D, quality analysis, and bioequivalence studies, we offer high-purity Fosnetupitant impurity reference standards, empowering research institutions and pharmaceutical companies to accelerate project timelines.

Key Features

Purity Assurance: HPLC purity ≥98%, with select batches reaching 99%. COA reports and HNMR, MS, HPLC spectra provided.
Structural Verification: Comprehensive data including IR, UV, and 2D NMR (COSY, NOESY, HMBC, HMQC) for unambiguous impurity identification.
Rapid Supply: In-stock availability with flexible packaging (10mg–100g). 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.