Keywords

• 6H-Purin-6-one,2-amino-1,9-dihydro-9-((2-(1-oxopropoxy)-1-((1-oxopropoxy)methyl)ethoxy)methyl)
• 2-[(2-amino-6-oxo-3,6-dihydro-9H-purin-9-yl)methoxy]propane-1,3-diyl dipropanoate
• 86357-20-2

Quick Details

• ProName: IMp. I (EP): 2-[(2-AMino-6-oxo-1,6-dih...
• CasNo: 86357-20-2
• Molecular Formula: C15H21N5O6
• Appearance: off-white powder
• 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

Ganciclovir Impurity Reference Standards

Ganciclovir impurity reference standards are indispensable tools in the fields of drug research and development, quality control, and pharmaceutical testing. Ganciclovir, as a highly effective and broad-spectrum antiviral drug, is widely used in clinical treatment. To ensure the purity and safety of Ganciclovir products, accurate identification and quantitative analysis of Ganciclovir and its impurities are crucial.

Our Ganciclovir impurity reference standards cover a variety of key impurities, including but not limited to Ganciclovir EP Impurity A, Ganciclovir Impurity C, Ganciclovir Impurity C-D5, and Ganciclovir Impurity H. These impurity reference standards have undergone rigorous quality control and purity testing to ensure they meet international and industry standards.

With Ganciclovir impurity reference standards, you can:

1. Accurately Identify Impurities: By comparing with impurity reference standards, you can quickly and accurately identify impurity components in pharmaceutical products.
2. Quantitatively Analyze Impurity Content: Utilize impurity reference standards for quantitative analysis to ensure that the impurity content in pharmaceutical products meets the specified standards.
3. Improve Pharmaceutical Quality Control: During pharmaceutical production and research and development, impurity reference standards can serve as important quality control tools to help improve the overall quality of pharmaceutical products.

We are committed to providing high-quality and high-purity Ganciclovir impurity reference standards to meet our customers' needs in drug research and development, quality control, and pharmaceutical testing.