CasNo.51496-03-8,diisopropylphenylphosphate,(51496-03-8) Suppliers

10 Milligram	Negotiable

Min.Order :10 Milligram
Purity: 95%+

Keywords

Diisopropylphenyl phosphate Sofosbuvir Impurity 51496-03-8

Quick Details

Appearance:off-white powder
Application:Pharmaceutical research
PackAge:Screw bottle,foil bags,Reagent bottles
ProductionCapacity:100|Gram|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:

Sofosbuvir Impurity Reference Standards

Sofosbuvir, as a highly effective antiviral drug, plays a crucial role in drug research and development, production, and quality control. The Sofosbuvir impurity reference standards we provide have been carefully prepared and rigorously tested to ensure their accuracy and reliability.

Product Features:

Comprehensive Range: Our product covers a wide range of Sofosbuvir impurities, including Impurity 1 to Impurity 41, to meet your needs at different research stages.
High Purity: All impurity reference standards are purified using advanced techniques such as High Performance Liquid Chromatography (HPLC), with purities exceeding 95%.
Structural Confirmation: Nuclear Magnetic Resonance (NMR) and Mass Spectrometry (MS) spectra are provided to ensure the accurate structure of the impurity reference standards.
Quality Assurance: Each batch of impurity reference standards is accompanied by a detailed Certificate of Analysis (COA) to ensure product quality traceability.

Applications:

Drug Research and Development: Used for new drug screening, pharmacodynamics evaluation, and toxicology studies.
Production Monitoring: As a quality control standard in the production process to ensure product stability.
Regulatory Compliance: To meet the regulatory requirements of domestic and foreign drug regulatory agencies for drug impurity control.