Keywords

• CyclosporinA, 6-[(3R,4R)-3-hydroxy-N,4-dimethyl-L-2-aminooctanoic acid]-
• 1,4,7,10,13,16,19,22,25,28,31-Undecaazacyclotritriacontane, cyclic peptidederiv.
• Cyclosporin A, dihydro-

Quick Details

• ProName: DIHYDROCYCLOSPORIN A
• CasNo: 59865-15-5
• Molecular Formula: C62H113N11O12
• 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

Cyclosporine Impurity Reference Standards

Cyclosporine impurity reference standards are crucial for drug development and quality control. Cyclosporine is a widely used immunosuppressant for preventing rejection reactions in allogeneic organ transplantations. To ensure the safety and efficacy of the drug, accurate detection and quantitative analysis of cyclosporine and its impurities are essential.

Our cyclosporine impurity reference standards cover a variety of cyclosporine impurities, including but not limited to Cyclosporine Impurity A, B, C, D, and more. These impurity reference standards have undergone rigorous quality control and purity testing to ensure they meet international and industry standards.

With cyclosporine impurity reference standards, you can:

1. Accurate Identification: By comparing with impurity reference standards, accurately identify impurity components in the drug.
2. Quantitative Analysis: Utilize impurity reference standards for quantitative analysis to ensure that the impurity content in the drug is within an acceptable range.
3. Quality Control: Use impurity reference standards for quality control during drug production and development to ensure product quality is stable and reliable.

We are committed to providing high-quality cyclosporine impurity reference standards to meet our customers' needs in drug development and quality control.